Разбор слова «подсолнечное»: для переноса, на слоги, по составу
Объяснение правил деление (разбивки) слова «подсолнечное» на слоги для переноса.
Онлайн словарь Soosle.ru поможет: фонетический и морфологический разобрать слово «подсолнечное» по составу, правильно делить на слоги по провилам русского языка, выделить части слова, поставить ударение, укажет значение, синонимы, антонимы и сочетаемость к слову «подсолнечное».
Содержимое:
- 1 Слоги в слове «подсолнечное» деление на слоги
- 2 Как перенести слово «подсолнечное»
- 3 Синонимы слова «подсолнечное»
- 4 Ударение в слове «подсолнечное»
- 5 Фонетическая транскрипция слова «подсолнечное»
- 6 Фонетический разбор слова «подсолнечное» на буквы и звуки (Звуко-буквенный)
- 7 Предложения со словом «подсолнечное»
- 8 Сочетаемость слова «подсолнечное»
- 9 Значение слова «подсолнечное»
- 10 Как правильно пишется слово «подсолнечное»
- 11 Ассоциации к слову «подсолнечное»
Слоги в слове «подсолнечное» деление на слоги
Количество слогов: 5
По слогам: по-дсо-лне-чно-е
По правилам школьной программы слово «подсолнечное» можно поделить на слоги разными способами. Допускается вариативность, то есть все варианты правильные. Например, такой:
под-сол-неч-но-е
По программе института слоги выделяются на основе восходящей звучности:
по-дсол-не-чно-е
Ниже перечислены виды слогов и объяснено деление с учётом программы института и школ с углублённым изучением русского языка.
л — непарная звонкая согласная (сонорная), примыкает к текущему слогу
ч примыкает к этому слогу, а не к предыдущему, так как не является сонорной (непарной звонкой согласной)
Как перенести слово «подсолнечное»
по—дсолнечное
под—солнечное
подсо—лнечное
подсол—нечное
подсолне—чное
подсолнеч—ное
Синонимы слова «подсолнечное»
1. дольний
2. земной
3. дольный
4. подлунный
5. подсолнечниковый
6. подсолнуховый
Ударение в слове «подсолнечное»
подсо́лнечное — ударение падает на 2-й слог
Фонетическая транскрипция слова «подсолнечное»
[пац`олн’ич’най’э]
Фонетический разбор слова «подсолнечное» на буквы и звуки (Звуко-буквенный)
Буква | Звук | Характеристики звука | Цвет |
---|---|---|---|
п | [п] | согласный, глухой парный, твёрдый, шумный | п |
о | [а] | гласный, безударный | о |
д | — | не образует звука | д |
с | [ц] | согласный, глухой непарный, твёрдый, шумный | с |
о | [`о] | гласный, ударный | о |
л | [л] | согласный, звонкий непарный (сонорный), твёрдый | л |
н | [н’] | согласный, звонкий непарный (сонорный), мягкий | н |
е | [и] | гласный, безударный | е |
ч | [ч’] | согласный, глухой непарный, мягкий, шипящий | ч |
н | [н] | согласный, звонкий непарный (сонорный), твёрдый | н |
о | [а] | гласный, безударный | о |
е | [й’] | согласный, звонкий непарный (сонорный), мягкий | е |
[э] | гласный, безударный |
Число букв и звуков:
На основе сделанного разбора делаем вывод, что в слове 12 букв и 12 звуков.
Буквы: 5 гласных букв, 7 согласных букв.
Звуки: 5 гласных звуков, 7 согласных звуков.
Предложения со словом «подсолнечное»
Разложенное на тарелки кушанье поливают подсолнечным маслом и посыпают зеленью петрушки и укропа.
Группа авторов, Великолепная рыбацкая и охотничья кухня, 2010.
У двери его лавки стоял автомат, который за монетку в один цент насыпал горсть подсолнечных семечек.
Ларри Кинг, Путь журналиста, 2009.
Широкие беспредельные степи, нивы и подсолнечные поля окружали дороги, по которым мы шли на восток.
Готтлоб Бидерман, В смертельном бою. Воспоминания командира противотанкового расчета. 1941-1945, 2005.
Сочетаемость слова «подсолнечное»
1. подсолнечное масло
2. подсолнечные семечки
3. подсолнечная шелуха
4. бутылка подсолнечного масла
5. литр подсолнечного масла
6. уже купила подсолнечное масло
7. (полная таблица сочетаемости)
Значение слова «подсолнечное»
ПОДСО́ЛНЕЧНЫЙ1 , -ая, -ое. Прил. к подсолнечник. Подсолнечные семечки. Подсолнечные жмыхи.
ПОДСО́ЛНЕЧНЫЙ2 , -ая, -ое. Трад.-поэт. 1. Существующий под солнцем; находящийся на земле, земной. (Малый академический словарь, МАС)
Как правильно пишется слово «подсолнечное»
Правописание слова «подсолнечное»
Орфография слова «подсолнечное»
Правильно слово пишется:
Нумерация букв в слове
Номера букв в слове «подсолнечное» в прямом и обратном порядке:
Ассоциации к слову «подсолнечное»
-
Семечко
-
Масло
-
Аннушка
-
Уксус
-
Чеснок
-
Перец
-
Макароны
-
Картошка
-
Сметана
-
Сковорода
-
Соль
-
Круп
-
Консервы
-
Капуста
-
Семя
-
Картофель
-
Огурец
-
Помидор
-
Морковь
-
Лакомство
-
Сало
-
Сахар
-
Гост
-
Ложка
-
Сковородка
-
Салат
-
Луковица
-
Жир
-
Волость
-
Лук
-
Чайная
-
Каша
-
Зелень
-
Мука
-
Квас
-
Сельсовет
-
Цистерна
-
Кастрюля
-
Сухарь
-
Перепись
-
Керосин
-
Переработка
-
Бутыль
-
Соус
-
Уезд
-
Овощ
-
Баранина
-
Молока
-
Кишечник
-
Приправа
-
Миска
-
Бутылка
-
Тара
-
Хозяйство
-
Яйцо
-
Начинка
-
Тест
-
Сахара
-
Бутылочка
-
Хлеб
-
Кислота
-
Оливковый
-
Всесоюзный
-
Кукурузный
-
Растительный
-
Льняной
-
Октябрьский
-
Бараний
-
Крестьянский
-
Литровый
-
Пшеничный
-
Пахучий
-
Жареный
-
Пальмовый
-
Троицкий
-
Ореховый
-
Хлебный
-
Рыбный
-
Свиной
-
Пищевой
-
Допотопный
-
Базарный
-
Съедобный
-
Полить
-
Жарить
-
Насчитываться
-
Перемешать
-
Смазать
-
Нарезать
-
Посыпать
-
Заправить
-
Разлить
-
Смесить
-
Поджарить
-
Смешать
-
Семенить
-
Проживать
-
Облить
-
Употребляться
-
Мелко
Как правильно пишется словосочетание «растительное масло»
- Как правильно пишется слово «растительный»
- Как правильно пишется слово «масло»
Делаем Карту слов лучше вместе
Привет! Меня зовут Лампобот, я компьютерная программа, которая помогает делать
Карту слов. Я отлично
умею считать, но пока плохо понимаю, как устроен ваш мир. Помоги мне разобраться!
Спасибо! Я стал чуточку лучше понимать мир эмоций.
Вопрос: намыкаться — это что-то нейтральное, положительное или отрицательное?
Ассоциации к словосочетанию «растительное масло»
Синонимы к словосочетанию «растительное масло»
Предложения со словосочетанием «растительное масло»
- Морковь, нарезанную кубиками, отварить в подсоленной воде, добавив ложку растительного масла и щепотку натёртой лимонной цедры.
- Смесь заправить растительным маслом, уксусом, чёрным перцем, посолить и перемешать.
- Для этого желток смешайте с мёдом, добавляйте растительное масло небольшими порциями.
- (все предложения)
Цитаты из русской классики со словосочетанием «растительное масло»
- Всего более мутил меня запах проклятого растительного масла, употребляемого китайцами в пищу; запах этот преследовал меня с Явы: там я почуял его в первый раз в китайской лавчонке и с той минуты возненавидел.
- Что ни фанза, то новый промысел: ловля жемчуга, добыча какого-то растительного масла, ханшина, корней острогала, да всего и не перечтешь.
- Прямые азиатские жиды: где их нет? и всюду разносят они запах чесноку, сандального дерева и растительного масла.
- (все
цитаты из русской классики)
Сочетаемость слова «масло»
- растительное масло
сливочное масло
оливковое масло - масло чайного дерева
масло лаванды
масло какао - ложка масла
на сковороде в растительном масле
запах масла - масло способствует
масло растаяло
масло закипит - обжарить в растительном масле
добавить масло
смазать маслом - (полная таблица сочетаемости)
Значение словосочетания «растительное масло»
-
Расти́тельные масла́, растительные жиры — продукты, извлекаемые из растительного сырья и состоящие из триглицеридов жирных кислот и сопутствующих им веществ (фосфолипиды, свободные жирные кислоты, воски, стеролы, вещества, придающие окраску и др.). (Википедия)
Все значения словосочетания РАСТИТЕЛЬНОЕ МАСЛО
Афоризмы русских писателей со словом «растительный»
- Истинное счастье — это прежде всего удел знающих, а не невежд. Человек, знающий, например, жизнь растений и законы растительного мира, гораздо счастливее того, кто даже не может отличить ольху от осины или клевер от подорожника.
- Человек, знающий, например, жизнь растений и законы растительного мира, гораздо счастливее того, кто даже не может отличить ольху от сосны или клевер от подорожника.
- (все афоризмы русских писателей)
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Дополнительно
Смотрите также
Расти́тельные масла́, растительные жиры — продукты, извлекаемые из растительного сырья и состоящие из триглицеридов жирных кислот и сопутствующих им веществ (фосфолипиды, свободные жирные кислоты, воски, стеролы, вещества, придающие окраску и др.).
Все значения словосочетания «растительное масло»
-
Морковь, нарезанную кубиками, отварить в подсоленной воде, добавив ложку растительного масла и щепотку натёртой лимонной цедры.
-
Смесь заправить растительным маслом, уксусом, чёрным перцем, посолить и перемешать.
-
Для этого желток смешайте с мёдом, добавляйте растительное масло небольшими порциями.
- (все предложения)
- постное масло
- масло
- сливочное масло
- оливковое масло
- топлёное масло
- (ещё синонимы…)
- масло
- (ещё ассоциации…)
- растительное масло
- продукты растительного происхождения
- обжарить в растительном масле
- (полная таблица сочетаемости…)
- растительное масло
- масло чайного дерева
- ложка масла
- масло способствует
- обжарить в растительном масле
- (полная таблица сочетаемости…)
- Разбор по составу слова «растительный»
- Разбор по составу слова «масло»
- Как правильно пишется слово «растительный»
- Как правильно пишется слово «масло»
Морфемный разбор слова:
Однокоренные слова к слову:
«МаслО» или «маслА» – как правильно пишется?
В диктантах, сочинениях, изложениях учащихся можно встретить разные ошибки: простые, сложные; типичные, редкие. Иногда совершенно понятное с точки зрения орфографии слово вызывает сомнение у пишущих. На помощь в этом случае приходят грамматика и этимология.
Значение и разбор слова
Выясним, как пишется масло. Итак, данная лексема оканчивается на букву о.
Это нарицательное имя существительное второго склонения, среднего рода, единственного числа, именительного падежа.
В предложении выполняет функцию подлежащего, в косвенных падежах – дополнения. В словосочетании занимает главную позицию, согласовывая в роде, числе и падеже зависимые имена прилагательные (вкусное, сливочное), порядковые числительные (первое, второе), определительные местоимения (всякое, каждое, иное).
Семантика: вещество, обладающее свойствами размягчения при повышенной температуре воздуха и затвердения при пониженной, использующееся для смазывания поверхности, намазывания на какой-либо предмет. Слово является многозначным, употребляется в прямом и переносном смысле.
Синонимы: мазь, смазка, бальзам, жир.
Правило орфографии
Правописание слова «масло» связано с этимологией лексемы. Конструкция появилась в русской речи из праславянского языка, аналогичные формы есть и в польском, и в украинском, и в сербском. Правописание слова запоминается, то есть лексема является словарной.
Примеры предложений
Растительное масло полезно для здоровья детей и взрослых, так как способствует усиленному пищеварению.
Оливковое масло – лучшая заправка для салатов из свежих овощей: помидоров, огурцов, болгарских перцев и зелени.
Анна Илларионовна положила сливочное масло в большую кастрюлю с дымящейся гречневой кашей и начала раскладывать еду по тарелкам всем членам многочисленной семьи Кузнецовых.
Читайте также, как пишутся другие проблемные слова:
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Ответ справочной службы русского языка
Ответ справочной службы русского языка
Рыбий жир – это определенный продукт, который получают из печени рыб. Рыбный жир – это в целом жир рыб. Так что, если составители СанПиН имели в виду второе, ошибки нет.
Добрый день! Подскажите, пожалуйста, как правильно написать: в составе крема маслО ши и монои или маслА ши и монои. Спасибо.
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Подскажите как правильно написать «четыре килограмма масла » или «четыре килограммов масла «?
Ответ справочной службы русского языка
Как правильно: не нужно добавлять маслА или маслО?
Ответ справочной службы русского языка
Ставится ли запятая в предложении: «Оцени(,) сколько масла нужно, чтобы приготовить суфле»? Спасибо.
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Вот какое слово есть в «Словаре русских народных говоров»:
Как правильно написать, в единственном или множественном числе. «В состав входят оливковое и подсолнечное масло» или «В состав входят оливковое и подсолнечное масла ». И почему?
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Так в чем вопрос-то? Форма мн. ч. используется, но при употреблении таких слов во мн. ч. меняется (или модифицируется) значение слова. Об этом и говорится в учебнике.
Уважаемые сотрудники грамотного портала! Очень надеюсь на ответ.
Можно ли в одном ряду оставить слова «мультимедийный» и «интерактивный» в заголовке? Не будет ли это маслом масляным?
«Методологические принципы разработки и функционирования инновационных образовательных интерактивных мультимедийных пособий для дошкольных образовательных учреждений»
Спасибо.
Ответ справочной службы русского языка
Скажите, пожалуйста, как пишется первая часть сложных слов «арома-«?
Знаю, что слово «ароматерапия» пишется вместе, а как написать «арома* масла «, «арома*сфера», «арома*талисман», и т.д.?
Очень надеюсь на скорый ответ!
Ответ справочной службы русского языка
Ответ справочной службы русского языка
как правильно: на основе масел мяты и миндаля или на основе масла мяты или миндаля?
Ответ справочной службы русского языка
Добрый день!
Подскажите, допустимо ли подобное написание: «массаж-релакс» (Ароматерапия: массаж-релакс, косметика для лица и тела, эфирные масла ).
Ответ справочной службы русского языка
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Добрый день!
Не будет ли » масло масляное » написание «Культурно-просветительский»?
Ответ справочной службы русского языка
Нет, сочетание культурно-просветительский корректно.
Добрый день! Как правильно писать: МаслЕный, маслЕННый или маслЯный?
Что-то является прилагательным, а что-то причастием, наверное, еще зависимое слово должно быть?
Ответ справочной службы русского языка
Грамотно ли сказать: в конечном итоге? Или это избыточно, как » масло масляное «?
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Словосочетание главный победитель нельзя назвать корректным: «неглавным», второстепенным победитель быть не может.
Уточняющий вопрос к вопросу №250741.
Повторюсь, как звучит предложение. «Это будет действительно эксклюзив, причем в единичном экземпляре». Скажите, а слово «эксклюзив» не подразумевает «нечто», изготовленное в единичном экземпляре? Не получается ли » масло масляное «.
Ответ справочной службы русского языка
Понятие «эксклюзив» не обязательно означает «единичный экземпляр».
Вопрос № 250125
Вопрос № 250072
«и обещает сделать это к июню месяцу.»
Ответ справочной службы русского языка
К сожалению, Вы ошибаетесь. Сочетания родовых и видовых наименований в русском языке очень частотны: город Москва, месяц июнь, сеть Интернет, животное корова и т. д. Выражение июнь месяц неграмотным не является. Более того, это и подобные выражения получают фиксацию в словарях русского языка: http://gramota.ru/slovari/dic/?word=*%EC%E5%F1%FF%F6&all=x
Скажите, пожалуйста, можно ли употреблять словосочетание «исламская мечеть» или это » масло масляное »
Спасибо
Ответ справочной службы русского языка
Добрый день!
Скажите, пожалуйста, правильно ли с точки зрения русского языка название «Отдел перспективного развития»? Или это » масло масляное «? Что-то в этом смущает.
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Возможно ли словосочетание «архивное хранение»? Это не » масло масляное «? Заранее спасибо.
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Верно: _ масло масляное _. Такое написание зафиксировано в словарях.
Ответ справочной службы русского языка
Это сочетание избыточно, правильно: _обслуживание техники_.
Ответ справочной службы русского языка
Источник
Теперь вы знаете какие однокоренные слова подходят к слову Как правильно пишется растительное масло, а так же какой у него корень, приставка, суффикс и окончание. Вы можете дополнить список однокоренных слов к слову «Как правильно пишется растительное масло», предложив свой вариант в комментариях ниже, а также выразить свое несогласие проведенным с морфемным разбором.
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Обозначь орфограмму, на которую нужно обратить внимание в каждом из данных слов. Образуй от этих слов наречия. Придумай и запиши сними словосочетания. Укажи главные и зависимые слова. Легкий- Дерзкий- Меткий- Жуткий —
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×òî òàêîå «ðàñòèòåëüíîå ìàñëî»? Êàê ïðàâèëüíî ïèøåòñÿ äàííîå ñëîâî. Ïîíÿòèå è òðàêòîâêà.
ðàñòèòåëüíîå ìàñëî ? ïèùåâûå æèðû
? èç, ñåìåíà
ìàñëî: ïîäñîëíå÷íîå.
ïîñòíîå ìàñëî. îëèâêîâîå. äåðåâÿííîå.
õëîïêîâîå. ëüíÿíîå. ñîåâîå. àðàõèäíîå. êîêîñîâîå.
êîíîïëÿíîå.
êàñòîðîâîå.
êóêóðóçíîå. ðàïñîâîå. êóíæóòíîå.
øðîò — îòæàòûå ñåìåíà ìàñëè÷íûõ ðàñòåíèé.
Расти́тельные масла́, растительные жиры — продукты, извлекаемые из растительного сырья и состоящие из триглицеридов жирных кислот и сопутствующих им веществ (фосфолипиды, свободные жирные кислоты, воски, стеролы, вещества, придающие окраску и др.).
Все значения словосочетания «растительное масло»
МА́СЛО, -а, мн. (спец., для обозначения различных сортов и видов) масла́, ма́сел, масла́м, ср. 1. Жировое вещество, получаемое из молока домашних животных, из семян, цветов или плодов некоторых растений и из веществ минерального происхождения. Топленое масло. Растительное масло. Эфирные масла. Смазочное масло.
Все значения слова «масло»
РАСТИ́ТЕЛЬНЫЙ, —ая, —ое. 1. Относящийся к растению (растениям). Растительный организм. Растительные вещества. Растительное происхождение.
Все значения слова «растительный»
-
В качестве основы для приготовления мази можно использовать и масла растительного происхождения – подсолнечное, оливковое.
-
Как было открыто сливочное масло, сосед по кухне и родственник по химическому составу масла растительного?
-
Требуется: 1/2 л воды, 120 г мяса, 150 г капусты квашеной, 10 г моркови, 10 г корня петрушки, 20 г лука репчатого, 50 г томатов консервированных, 10 г масла растительного, 2 г чеснока, 2 г сахара, 20 г сметаны, соль, зелень по вкусу.
- (все предложения)
- масло сливочное
- сливочное масло
- столовая ложка растительного масла
- кукуруза консервированная
- спаржевая фасоль
- (ещё синонимы…)
- масло
- (ещё ассоциации…)
- елей
- молоко
- маслина
- касторка
- маслозавод
- (ещё ассоциации…)
- растительность
- травоядные
- (ещё ассоциации…)
- Разбор по составу слова «масло»
- Разбор по составу слова «растительный»
- Как правильно пишется слово «масло»
- Как правильно пишется слово «растительный»
Содержание
- «МаслО» или «маслА» – как правильно пишется?
- Значение и разбор слова
- Правило орфографии
- Примеры предложений
- Поиск ответа
- Растительное и подсолнечное масло: отличия
- Что нужно знать о растительном масле
- Подсолнечное масло
- Схожесть и различие подсолнечного и растительного масел
- Сорта растительных масел
- Полезные свойства растительного масла
- Выбор масла
- Как правильно: масляный или масленый?
- Новости на эту же тему
- Фоторепортажи
«МаслО» или «маслА» – как правильно пишется?
В диктантах, сочинениях, изложениях учащихся можно встретить разные ошибки: простые, сложные; типичные, редкие. Иногда совершенно понятное с точки зрения орфографии слово вызывает сомнение у пишущих. На помощь в этом случае приходят грамматика и этимология.
Значение и разбор слова
Выясним, как пишется масло. Итак, данная лексема оканчивается на букву о.
Это нарицательное имя существительное второго склонения, среднего рода, единственного числа, именительного падежа.
В предложении выполняет функцию подлежащего, в косвенных падежах – дополнения. В словосочетании занимает главную позицию, согласовывая в роде, числе и падеже зависимые имена прилагательные (вкусное, сливочное), порядковые числительные (первое, второе), определительные местоимения (всякое, каждое, иное).
Семантика: вещество, обладающее свойствами размягчения при повышенной температуре воздуха и затвердения при пониженной, использующееся для смазывания поверхности, намазывания на какой-либо предмет. Слово является многозначным, употребляется в прямом и переносном смысле.
Синонимы: мазь, смазка, бальзам, жир.
Правило орфографии
Правописание слова «масло» связано с этимологией лексемы. Конструкция появилась в русской речи из праславянского языка, аналогичные формы есть и в польском, и в украинском, и в сербском. Правописание слова запоминается, то есть лексема является словарной.
Примеры предложений
Растительное масло полезно для здоровья детей и взрослых, так как способствует усиленному пищеварению.
Оливковое масло – лучшая заправка для салатов из свежих овощей: помидоров, огурцов, болгарских перцев и зелени.
Анна Илларионовна положила сливочное масло в большую кастрюлю с дымящейся гречневой кашей и начала раскладывать еду по тарелкам всем членам многочисленной семьи Кузнецовых.
Читайте также, как пишутся другие проблемные слова:
Источник
Поиск ответа
Добрый день!
Не будет ли » масло масляное » написание «Культурно-просветительский»?
Ответ справочной службы русского языка
Нет, сочетание культурно-просветительский корректно.
Добрый день! Как правильно писать: МаслЕный, маслЕННый или маслЯный?
Что-то является прилагательным, а что-то причастием, наверное, еще зависимое слово должно быть?
Ответ справочной службы русского языка
Грамотно ли сказать: в конечном итоге? Или это избыточно, как » масло масляное «?
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Словосочетание главный победитель нельзя назвать корректным: «неглавным», второстепенным победитель быть не может.
Уточняющий вопрос к вопросу №250741.
Повторюсь, как звучит предложение. «Это будет действительно эксклюзив, причем в единичном экземпляре». Скажите, а слово «эксклюзив» не подразумевает «нечто», изготовленное в единичном экземпляре? Не получается ли » масло масляное «.
Ответ справочной службы русского языка
Понятие «эксклюзив» не обязательно означает «единичный экземпляр».
Вопрос № 250125
Вопрос № 250072
«и обещает сделать это к июню месяцу.»
Ответ справочной службы русского языка
К сожалению, Вы ошибаетесь. Сочетания родовых и видовых наименований в русском языке очень частотны: город Москва, месяц июнь, сеть Интернет, животное корова и т. д. Выражение июнь месяц неграмотным не является. Более того, это и подобные выражения получают фиксацию в словарях русского языка: http://gramota.ru/slovari/dic/?word=*%EC%E5%F1%FF%F6&all=x
Скажите, пожалуйста, можно ли употреблять словосочетание «исламская мечеть» или это » масло масляное »
Спасибо
Ответ справочной службы русского языка
Добрый день!
Скажите, пожалуйста, правильно ли с точки зрения русского языка название «Отдел перспективного развития»? Или это » масло масляное «? Что-то в этом смущает.
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Возможно ли словосочетание «архивное хранение»? Это не » масло масляное «? Заранее спасибо.
Ответ справочной службы русского языка
Ответ справочной службы русского языка
Верно: _ масло масляное _. Такое написание зафиксировано в словарях.
Ответ справочной службы русского языка
Это сочетание избыточно, правильно: _обслуживание техники_.
Ответ справочной службы русского языка
Источник
Растительное и подсолнечное масло: отличия
Различают несколько разновидностей растительных масел, и подсолнечное тоже входит в их число. Кстати, Россия является одной из ведущих стран, производящих именно подсолнечное масло. Для того, чтобы разобраться в этом вопросе более подробно, рекомендуется знать несколько интересных фактов о растительных маслах и о том, как лучше употреблять их в пищу.
Различают несколько разновидностей растительных масел, и подсолнечное тоже входит в их число. Кстати, Россия является одной из ведущих стран, производящих именно подсолнечное масло. Для того, чтобы разобраться в этом вопросе более подробно, рекомендуется знать несколько интересных фактов о растительных маслах и о том, как лучше употреблять их в пищу.
Что нужно знать о растительном масле
Масло растительного происхождения — один из популярных видов жиров. Мы заправляем им салаты и жарим на нём продукты. Извлечение любого растительного масла производится так: нагретые либо измельчённые семена или плоды отжимают по особой технологии, а культуры, используемые для производства такой продукции, относят к масленичным. Консистенция растительного масла бывает разной:
Методов получения масел (отжимов) тоже несколько. Они бывают:
Различают нерафинированное растительное масло, получаемое после того, как его отфильтруют от примесей. В нём сохранены все ценные вещества вместе с запахом и вкусовыми качествами. Такое масло густое, имеет насыщенный цвет, а если его долго хранить, оно начинает постепенно выделять осадок. Им идеально заправлять любые салаты, а вот жарка на нём проблематична.
Рафинированные масла подвергают, как минимум, нескольким методам очистки, кроме фильтрации. Обычно их нейтрализуют с помощью щелочного состава. Такой продукт не имеет ни запаха, ни вкуса. Он прекрасно выдерживает хранение и как раз предназначен для жарки. Дыма и пены во время жарки рафинированное масло почти не даёт, поэтому в кулинарных целях его применять идеально.
Бывают ещё гидратированные масла, очищаемые горячей водой. При очистке воду распыляют особым образом, а сам продукт — прозрачный, без мути и примесей, не имеющий никакого осадка.
Дезодорированные масла готовят путём очистки горячим паром. При этом используют вакуумную методику. У масла тоже отсутствуют вкус, цвет и запах.
Любое растительное масло является высококалорийным продуктом, так как состоит из жира почти на сто процентов. Конечно, убирать его из рациона питания не рекомендуется, даже если человек соблюдает очень строгую диету. Дефицит растительных масел в организме чреват быстрым появлением недостатка витамина Е, а также всех типов жирных кислот, участвующих в формировании клеток.
Подсолнечное масло
Как уже было сказано, этот вид масла получают из подсолнечных семечек. Почти все маслоэкстракционные заводы изготавливают подсолнечное масло с соблюдением непростого технологического процесса. Вначале семена подсолнечника помещают в рушально-веечное отделение, где их тщательно очищают, а затем обрушивают, отделяя лузгу от ядрышек. После этого семечки попадают в вальцевый цех, где ядра обрабатывают вальцами. В результате получается мятка, которую помещают в отдел прессования. Там есть специальные жаровни, где масло подвергают тепловой обработке и отжимают.
После отжима продукт отстаивают и хранят в течение некоторого времени. Масса, получаемая в процессе обработки, называется мезга. Её обрабатывают в маслоэкстракционном цехе и получают смесь, которую в дальнейшем используют в качестве корма для домашних животных и птиц.
После хранения и отстаивания масло отправляют в экстрактор. Это специальный аппарат для экстрагирования продукта с помощью растворителей органического происхождения. В результате экстрагирования получаются:
Из мисцеллы и шрота масло отгоняют в экстракторе, затем очищают (рафинируют), убирая из него органические примеси. Есть несколько стадий рафинирования, которые отличаются сложностью и последовательностью процесса. В целом, изготавливают масло долго, с применением сложных технологий, но результатом становится полезный продукт, доступный для каждого потребителя.
Схожесть и различие подсолнечного и растительного масел
Как уже было сказано, подсолнечное масло — это разновидность растительного, а сырьём для его изготовления служат подсолнечные семечки. Отличия подсолнечного масла от других видов этого продукта тоже есть, например:
Кроме подсолнечного масла, желающие всегда могут выбрать в магазинах и другие виды масел, так как каждый из них приносит организму определённую пользу.
Сорта растительных масел
Сортов растительных масел много и среди них различают следующие:
Тем не менее, лечиться оливковым маслом без предварительной консультации с врачом нельзя.
Полезные свойства растительного масла
Люди, которые стараются вести здоровый образ жизни, всегда употребляют в пищу растительное масло. Прежде всего, любой его вид богат содержанием:
Любое растительное масло хорошего качества улучшает работу желудка и кишечника, способствует очищению организма от «плохого» холестерина и других вредных веществ. Главное — чтобы продукт был изготовлен именно из полезного сырья, с применением корректных производственных технологий. Некоторые специалисты рекомендуют отдавать приоритет маслу, не подвергавшемуся искусственной обработке (рафинированию, дезодорированию и проч.). Считается, что масло, при производстве которого был применён холодный отжим, самое полезное, при условии минимальной обработки. Безусловно, чем короче её процесс, тем больше полезных компонентов сохраняет продукт. Например, под воздействием высоких температур при нагревании сырья много витаминов теряется, поэтому сторонники здорового образа жизни предпочитают покупать нерафинированные виды масел.
Выбор масла
Эксперты «Росконтроля», изучив технологии изготовления и состав известных в России марок растительного масла, подготовили их рейтинг, на основании которого потребители могут судить об их пользе, популярности и соответствии нормативам, установленным ГОСТ.
На первом месте находится подсолнечное масло марки «Слобода». При его производстве были соблюдены все необходимые правила безопасности, а характеристики и состав, описанные на этикетке, полностью соответствуют действительности, равно как и сорт продукта — высший. Употреблять его в пищу можно без всякого опасения.
На второе место эксперты поставили масло «Мистер Рикко». Его тестировали впервые, не выявив никаких серьёзных недостатков, поэтому и рекомендуют к покупке. Раньше сотрудники «Росконтроля» не знали, как им относиться к этой марке, но после тщательного тестирования они утверждают, что ей можно доверять.
На третьем месте находится известное масло «Олейна». Оно в изобилии содержит линолевую кислоту, мало в чём уступая другим видам масла по основным характеристикам. Масло «Олейна» до сих пор считают продуктом первого сорта, хотя, по идее, оно вполне могло бы претендовать и на высший сорт.
Четвёртое место эксперты отдали растительному маслу «Злато». Для продукта первого сорта оно обладает вполне приличными качествами и произведено в полном соответствии со всеми требованиями безопасности. Все показатели производства досконально проверены специалистами.
На пятом месте — масло «Золотая семечка». У него оказался завышенным только один из показателей, но пределов нормы он не превышает.
Масло «Благо», к сожалению, попало на шестое место, так как производитель позиционирует его как продукт класса премиум, которому оно точно не соответствует. Это показал лабораторный анализ. Что касается его пригодности к употреблению в пищу, с этим проблем не возникает.
Источник
Как правильно: масляный или масленый?
Выбор буквы в этом случае зависит от значения слова.
Администрация города Екатеринбурга в рамках проекта «Екатеринбург говорит правильно» обращается к вопросу о корректном написании слов масленый и масляный.
Как отмечает справочно-информационный портал «Русский язык», выбор буквы в этом случае зависит от значения слова, однако ударение всегда остается на первом слоге.
Масленый пишется в следующих случаях:
— покрытый, испачканный, пропитанный маслом (масленые руки);
— выражающий чувственность, вожделение (о глазах, взгляде) (следить маслеными глазами);
— слащавый, льстивый, заискивающий (масленый голосок).
Слово масляный же употребляется в других значениях:
— разведенный на масле (масляные краски);
— относящийся к маслу или соотнесенный с ним, свойственный маслу, работающий на масле (масляный насос);
— написанный масляными красками (масляный портрет).
Таким образом, правильно: масленый пирог, масленый взгляд, масляный крем.
Фото www.yandex.ru
Новости на эту же тему
Это первое дошкольное учреждение Ленинского района с собственным бассейном.
Здание учреждения было законсервировано с 2013 года.
В олимпиаде приняли участие 279 учащихся.
Фоторепортажи
На Официальном портале Екатеринбурга расположена наиболее полная информация о городе и его истории, опубликованы новости Екатеринбурга и его окрестностей, фоторепортажи. Городской портал Екатеринбурга содержит справочные материалы: афиша театров и кино, информация о погоде, каталог предприятий Екатеринбурга, пробки в Екатеринбурге, полная структура органов местного самоуправления, таких как Администрация города Екатеринбурга. Большое количество официальных документов размещено в разделах «Официально», «Власть Екатеринбурга».
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Источник
Vegetable oils, or vegetable fats, are oils extracted from seeds or from other parts of fruits. Like animal fats, vegetable fats are mixtures of triglycerides.[1] Soybean oil, grape seed oil, and cocoa butter are examples of seed oils, or fats from seeds. Olive oil, palm oil, and rice bran oil are examples of fats from other parts of fruits. In common usage, vegetable oil may refer exclusively to vegetable fats which are liquid at room temperature.[2][3] Vegetable oils are usually edible.
Uses[edit]
In antiquity[edit]
Oils extracted from plants have been used since ancient times and in many cultures. Archaeological evidence shows that olives were turned into olive oil by 6000 BCE[4] and 4500 BCE in present-day Israel and Palestine.[5]
In addition to use as food, fats and oils (both vegetable and mineral) have long been used as fuel, typically in lamps which were a principal source of illumination in ancient times. Oils may have been used for lubrication, but there is no evidence for this. Vegetable oils were probably more valuable as food and lamp-oil;[citation needed] Babylonian mineral oil was known to be used as fuel, but there are no references to lubrication. Pliny the Elder reported that animal-derived fats such as lard were used to lubricate the axles of carts.[6]
Culinary[edit]
Many vegetable oils are consumed directly, or indirectly as ingredients in food – a role that they share with some animal fats, including butter, ghee, lard, and schmaltz. The oils serve a number of purposes in this role:
- Shortening – as in giving pastries a crumbly texture.
- Enriching – adding calories and satisfaction in consumption
- Texture – altering how ingredients combine, especially fats and starches
- Flavoring – examples include olive, sesame, or almond oil
- Flavor base – oils can also «carry» flavors of other ingredients, such as peppers,[7] since many flavors are due to chemicals that are soluble in oil.
Oils can be heated to temperatures significantly higher than the boiling point of water, 100 °C (212 °F), and used to fry foods. Oils for this purpose must have a high flash point. Such oils include both the major cooking oils – soybean, rapeseed, canola, sunflower, safflower, peanut, cottonseed, etc. – and tropical oils, such as coconut, palm, and rice bran. The latter are particularly valued in Asian cultures for high-temperature cooking, because of their unusually high flash points.
Industrial[edit]
Vegetable oils are used as an ingredient or component in many manufactured products.
Many vegetable oils are used to make soaps, skin products, candles, perfumes and other personal care and cosmetic products. Some oils are particularly suitable as drying oils, and are used in making paints and other wood treatment products. They are used in alkyd resin production. Dammar oil (a mixture of linseed oil and dammar resin), for example, is used almost exclusively in treating the hulls of wooden boats. Vegetable oils are increasingly being used in the electrical industry as insulators as vegetable oils are not toxic to the environment, biodegradable if spilled and have high flash and fire points. However, vegetable oils are less stable chemically, so they are generally used in systems where they are not exposed to oxygen, and they are more expensive than crude oil distillate. Synthetic tetraesters, which are similar to vegetable oils but with four fatty acid chains compared to the normal three found in a natural ester, are manufactured by Fischer esterification. Tetraesters generally have high stability to oxidation and have found use as engine lubricants. Vegetable oil is being used to produce biodegradable hydraulic fluid[8] and lubricant.[9]
One limiting factor in industrial uses of vegetable oils is that all such oils are susceptible to becoming rancid. Oils that are more stable, such as ben oil or mineral oil, are thus preferred for industrial uses. Castor oil has numerous industrial uses, owing to the presence of hydroxyl group on the fatty acid. Castor oil is a precursor to Nylon 11. Castor oil may also be reacted with epichlorohydrin to make a glycidyl ether which is used as a diluent and flexibilizer with epoxy resins.
Pet food additive[edit]
Vegetable oil is used in the production of some pet foods. AAFCO[10] defines vegetable oil in this context as the product of vegetable origin obtained by extracting the oil from seeds or fruits which are processed for edible purposes.
Fuel[edit]
Vegetable oils are also used to make biodiesel, which can be used like conventional diesel. Some vegetable oil blends are used in unmodified vehicles but straight vegetable oil, also known as pure plant oil, needs specially prepared vehicles which have a method of heating the oil to reduce its viscosity. The use of vegetable oils as alternative energy is growing[citation needed] and the availability of biodiesel around the world is increasing.[citation needed]
The NNFCC estimates that the total net greenhouse gas savings when using vegetable oils in place of fossil fuel-based alternatives for fuel production, range from 18 to 100%.[11]
Production[edit]
The production process of vegetable oil involves the removal of oil from plant components, typically seeds. This can be done via mechanical extraction using an oil mill or chemical extraction using a solvent. The extracted oil can then be purified and, if required, refined or chemically altered.
[edit]
Oils can be removed via mechanical extraction, termed «crushing» or «pressing.» This method is typically used to produce the more traditional oils (e.g., olive, coconut etc.), and it is preferred by most health-food customers in the United States and in Europe.[citation needed] There are several different types of mechanical extraction.[12] Expeller pressing extraction is common, though the screw press, ram press, and ghani (powered mortar and pestle) are also used. Oilseed presses are commonly used in developing countries, among people for whom other extraction methods would be prohibitively expensive; the ghani is primarily used in India.[13] The amount of oil extracted using these methods varies widely, as shown in the following table for extracting mowrah butter in India:[14]
Method | Percentage extracted |
---|---|
Ghani[15] | 20–30% |
Expellers | 34–37% |
Solvent | 40–43% |
[edit]
The processing of vegetable oil in commercial applications is commonly done by chemical extraction, using solvent extracts, which produces higher yields and is quicker and less expensive. The most common solvent is petroleum-derived hexane. This technique is used for most of the «newer» industrial oils such as soybean and corn oils. After extraction, the solvent is evaporated out by heating the mixture to about 300 °F (149 °C).[16]
Supercritical carbon dioxide can be used as a non-toxic alternative to other solvents.[17]
Hydrogenation[edit]
Unsaturated vegetable oils can be transformed through partial or complete hydrogenation into oils of higher melting point, some of which, such as vegetable shortening, will remain solid at room temperature.
Hydrogenating vegetable oil is done by raising a blend of vegetable oil and a metal catalyst, typically nickel, in near-vacuum to very high temperatures, and introducing hydrogen. This causes the carbon atoms of the oil to break double-bonds with other carbons. Each carbon atom becomes single-bonded to an individual hydrogen atom, and the double bond between carbons can no longer exist. A fully hydrogenated oil, also called a saturated fat, has had all of its double bonds converted into single bonds. If a polyunsaturated oil is left incompletely-hydrogenated (not all of the double bonds are reduced to single bonds), then it is a «partially hydrogenated oil» (PHO). An oil may be hydrogenated to increase resistance to rancidity (oxidation) or to change its physical characteristics. As the degree of saturation is raised by full or partial hydrogenation, the oil’s viscosity and melting point increase.
While full hydrogenation produces largely saturated fatty acids, partial hydrogenation results in the transformation of unsaturated cis fatty acids to unsaturated trans fatty acids in the oil mixture due to the heat used in hydrogenation. Partially hydrogenated oils and their trans fats have been linked to an increased risk of mortality from coronary heart disease,[18] among other increased health risks. These concerns have led to regulations mandating the removal of partially hydrogenated oils from food.[19]
Deodorization[edit]
In the processing of edible oils, the oil is heated under vacuum to near the smoke point or to about 450 °F (232 °C),[20] and water is introduced at the bottom of the oil. The water immediately is converted to steam, which bubbles through the oil, carrying with it any chemicals which are water-soluble. The steam sparging removes impurities that can impart unwanted flavors and odors to the oil. Deodorization is key to the manufacture of vegetable oils. Nearly all soybean, corn, and canola oils found on supermarket shelves go through a deodorization stage that removes trace amounts of odors and flavors, and lightens the color of the oil. However, the process commonly results in higher levels of trans fatty acids and distillation of the oil’s natural compounds.[21][22][23]
Occupational exposure[edit]
People can breathe in vegetable oil mist in the workplace. The U.S. Occupational Safety and Health Administration (OSHA) has set the legal limit (permissible exposure limit) for vegetable oil mist exposure in the workplace as 15 mg/m3 total exposure and 5 mg/m3 respiratory exposure over an 8-hour workday. The U.S. National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 10 mg/m3 total exposure and 5 mg/m3 respiratory exposure over an 8-hour workday.[24]
Yield[edit]
Typical productivity of some oil crops, measured in tons (t) of oil produced per hectare (ha) of land per year (yr). Oil palm is by far the highest yielding crop, capable of producing about 4 tons of palm oil per hectare per year.
Crop | Yield (t/ha/yr) |
---|---|
Palm oil [25] | 4.0 |
Coconut oil [26] | 1.4 |
Canola oil [27] | 1.4 |
Soybean oil [27] | 0.6 |
Sunflower oil [26] | 0.6 |
Particular oils[edit]
The following triglyceride vegetable oils account for almost all worldwide production, by volume. All are used as both cooking oils and as SVO or to make biodiesel. According to the USDA, the total world consumption of major vegetable oils in 2007/08 was:[28]
Oil source | World consumption (million metric tons) |
Notes |
---|---|---|
Palm | 41.31 | The most widely produced tropical oil, also used to make biofuel |
Soybean | 41.28 | One of the most widely consumed cooking oils |
Rapeseed | 18.24 | One of the most widely used cooking oils, also used as fuel. Canola is a variety (cultivar) of rapeseed. |
Sunflower seed | 9.91 | A common cooking oil, also used to make biodiesel |
Peanut | 4.82 | Mild-flavored cooking oil |
Cottonseed | 4.99 | A major food oil, often used in industrial food processing |
Palm kernel | 4.85 | From the seed of the African palm tree |
Coconut | 3.48 | Used in cooking, cosmetics and soaps |
Olive | 2.84 | Used in cooking, cosmetics, soaps and as a fuel for traditional oil lamps |
Note that these figures include industrial and animal feed use. The majority of European rapeseed oil production is used to produce biodiesel, or used directly as fuel in diesel cars which may require modification to heat the oil to reduce its higher viscosity.
Other significant oils include:
- Corn oil, one of the most common cooking oils, is used for cooking oil, salad dressing, margarine, mayonnaise, prepared goods like spaghetti sauce and baking mixes, and to fry prepared foods like potato chips and French fries.
- Grape seed oil, used in cooking and cosmetics
- Hazelnut oil and other nut oils
- Linseed oil, from flax seeds
- Rice bran oil, from rice grains
- Safflower oil, a flavorless and colorless cooking oil
- Sesame oil, used as a cooking oil, and as a massage oil, particularly in India
- Açaí palm oil, used in culinary and cosmetics
- Jambú oil, is extracted from the flowers, leaves and stem from jambu (Acmella oleracea), contains spilanthol
- Graviola oil, derived from Annona muricata
- Tucumã oil, from Astrocaryum aculeatum is used to manufacture soap.
- Brazil nut oil, culinary and cosmetics use
- Carapa oil, pharmaceutical use and anti-mosquito candle
- Buriti oil, from Mauritia flexuosa, used in cosmetics (skin and hair care)
- Passion fruit oil, derived from Passiflora edulis, has varied applications in cosmetics manufacturing and for uses as a human or animal food.
- Pracaxi oil, obtained from Pentaclethra macroloba, cosmetics use
- Solarium oil, derived from chloroplasts, various applications in cooking
Composition of fats[edit]
Properties of vegetable oils[29][30]
The nutritional values are expressed as percent (%) by mass of total fat. | |||||||||
Type | Processing treatment[31] |
Saturated fatty acids |
Monounsaturated fatty acids |
Polyunsaturated fatty acids |
Smoke point | ||||
---|---|---|---|---|---|---|---|---|---|
Total[29] | Oleic acid (ω-9) |
Total[29] | α-Linolenic acid (ω-3) |
Linoleic acid (ω-6) |
ω-6:3 ratio |
||||
Avocado[32] | 11.6 | 70.6 | 52–66[33] | 13.5 | 1 | 12.5 | 12.5:1 | 250 °C (482 °F)[34] | |
Brazil nut[35] | 24.8 | 32.7 | 31.3 | 42.0 | 0.1 | 41.9 | 419:1 | 208 °C (406 °F)[36] | |
Canola[37] | 7.4 | 63.3 | 61.8 | 28.1 | 9.1 | 18.6 | 2:1 | 238 °C (460 °F)[36] | |
Coconut[38] | 82.5 | 6.3 | 6 | 1.7 | 175 °C (347 °F)[36] | ||||
Corn[39] | 12.9 | 27.6 | 27.3 | 54.7 | 1 | 58 | 58:1 | 232 °C (450 °F)[40] | |
Cottonseed[41] | 25.9 | 17.8 | 19 | 51.9 | 1 | 54 | 54:1 | 216 °C (420 °F)[40] | |
Cottonseed[42] | hydrogenated | 93.6 | 1.5 | 0.6 | 0.2 | 0.3 | 1.5:1 | ||
Flaxseed/linseed[43] | 9.0 | 18.4 | 18 | 67.8 | 53 | 13 | 0.2:1 | 107 °C (225 °F) | |
Grape seed | 10.5 | 14.3 | 14.3 | 74.7 | – | 74.7 | very high | 216 °C (421 °F)[44] | |
Hemp seed[45] | 7.0 | 9.0 | 9.0 | 82.0 | 22.0 | 54.0 | 2.5:1 | 166 °C (330 °F)[46] | |
Olive[47] | 13.8 | 73.0 | 71.3 | 10.5 | 0.7 | 9.8 | 14:1 | 193 °C (380 °F)[36] | |
Palm[48] | 49.3 | 37.0 | 40 | 9.3 | 0.2 | 9.1 | 45.5:1 | 235 °C (455 °F) | |
Palm[49] | hydrogenated | 88.2 | 5.7 | 0 | |||||
Peanut[50] | 16.2 | 57.1 | 55.4 | 19.9 | 0.318 | 19.6 | 61.6:1 | 232 °C (450 °F)[40] | |
Rice bran oil | 25 | 38.4 | 38.4 | 36.6 | 2.2 | 34.4[51] | 15.6 | 232 °C (450 °F)[52] | |
High-oleic safflower oil[53] | 7.5 | 75.2 | 75.2 | 12.8 | 0 | 12.8 | very high | 212 °C (414 °F)[36] | |
Sesame[54] | 14.2 | 39.7 | 39.3 | 41.7 | 0.3 | 41.3 | 138:1 | ||
Soybean[55] | 15.6 | 22.8 | 22.6 | 57.7 | 7 | 51 | 7.3:1 | 238 °C (460 °F)[40] | |
Soybean[56] | partially hydrogenated | 14.9 | 43.0 | 42.5 | 37.6 | 2.6 | 34.9 | 13.4:1 | |
Walnut oil[57] | unrefined | 9.1 | 22.8 | 22.2 | 63.3 | 10.4 | 52.9 | 5:1 | 160 °C (320 °F)[58] |
Sunflower[59] | 8.99 | 63.4 | 62.9 | 20.7 | 0.16 | 20.5 | 128:1 | 227 °C (440 °F)[40] |
Seed oil[edit]
Seed oils are vegetable oils obtained from the seed (endosperm) of some plants, rather than the fruit (pericarp). Most vegetable oils are seed oils. Examples are sunflower, corn, and sesame oils.
Pre-pressing[edit]
Extracting the oils first by expeller or cold pressing methods, then solvent expelling the rest of the oils from the leftover matter. This is a method used by larger capacity oil mills. As the energy consumption of the mechanical press increases as more oil is released, it is more efficient to extract the rest of the oil (past around 60%) by solvent extraction.[60]
History[edit]
Such oils have been part of human culture for millennia.[4] Oils such as poppy seed, rapeseed, linseed, almond oil, sesame seed, safflower, and cottonseed were variously used since at least the Bronze Age in the Middle East.[4] Vegetable oils have been used for lighting fuel, cooking, medicine and lubrication.
Palm oil has long been recognized in West and Central African countries, and European merchants trading with West Africa occasionally purchased palm oil for use as a cooking oil in Europe and it became highly sought-after commodity by British traders for use as an industrial lubricant for machinery during Britain’s Industrial Revolution.[61] Palm oil formed the basis of soap products, such as Lever Brothers’ (now Unilever) «Sunlight», and
B. J. Johnson Company’s (now Colgate-Palmolive) «Palmolive»,[62] and by around 1870, palm oil constituted the primary export of some West African countries.[63]
In 1780 Carl Wilhelm Scheele demonstrated that fats were derived from glycerol. Thirty years later Michel Eugène Chevreul deduced that these fats were esters of fatty acids and glycerol. Wilhelm Normann, a German chemist introduced the hydrogenation of liquid fats in 1901, creating what later became known as trans fats, leading to the development of the global production of margarine and vegetable shortening.
In the USA cottonseed oil was developed, and marketed by Procter & Gamble as a creamed shortening – Crisco – as early as 1911. Ginning mills were happy to have someone haul away the cotton seeds. The extracted oil was refined and partially hydrogenated to give a solid at room temperature and thus mimic natural lard, and canned under nitrogen gas. Compared to the rendered lard Procter & Gamble was already selling to consumers, Crisco was cheaper, easier to stir into a recipe, and could be stored at room temperature for two years without turning rancid.
Soybeans are protein-rich, and the medium viscosity oil rendered from them was high in polyunsaturates. Henry Ford established a soybean research laboratory, developed soybean plastics and a soy-based synthetic wool, and built a car «almost entirely» out of soybeans.[64] Roger Drackett had a successful new product with Windex, but he invested heavily in soybean research, seeing it as a smart investment.[65] By the 1950s and 1960s, soybean oil had become the most popular vegetable oil in the US; today it is second only to palm oil. In 2018–2019, world production was at 57.4 MT with the leading producers including China (16.6 MT), US (10.9 MT), Argentina (8.4 MT), Brazil (8.2 MT), and EU (3.2 MT).[66]
The early 20th century also saw the start of the use of vegetable oil as a fuel in diesel engines and in heating oil burners. Rudolf Diesel designed his engine to run on vegetable oil. The idea, he hoped, would make his engines more attractive to farmers having a source of fuel readily available. Diesel’s first engine ran on its own power for the first time in Augsburg, Germany, on 10 August 1893 on nothing but peanut oil. In remembrance of this event, 10 August has been declared «International Biodiesel Day».[67] The first patent on Biodiesel was granted in 1937.[68] Periodic petroleum shortages spurred research into vegetable oil as a diesel substitute during the 1930s and 1940s, and again in the 1970s and early 1980s when straight vegetable oil enjoyed its highest level of scientific interest. The 1970s also saw the formation of the first commercial enterprise to allow consumers to run straight vegetable oil in their vehicles. However, biodiesel, produced from oils or fats using transesterification is more widely used. It is Led by Brazil, many countries built biodiesel plants during the 1990s, and it is now widely available for use in motor vehicles, and is the most common biofuel in Europe today. In France, biodiesel is incorporated at a rate of 8% in the fuel used by all French diesel vehicles.[69]
In the mid-1970s, Canadian researchers developed a low-erucic-acid rapeseed cultivar. Because the word «rape» was not considered optimal for marketing, they coined the name «canola» (from «Canada Oil low acid»). The U.S. Food and Drug Administration approved use of the canola name in January 1985,[70] and U.S. farmers started planting large areas that spring. Canola oil is lower in saturated fats, and higher in monounsaturates. Canola is very thin (unlike corn oil) and flavorless (unlike olive oil), so it largely succeeds by displacing soy oil, just as soy oil largely succeeded by displacing cottonseed oil.
Used oil[edit]
A large quantity of used vegetable oil is produced and recycled, mainly from industrial deep fryers in potato processing plants, snack food factories and fast food restaurants.
Recycled oil has numerous uses, including use as a direct fuel, as well as in the production of biodiesel, livestock feed, pet food, soap, detergent, cosmetics, and industrial chemicals.
Since 2002, an increasing number of European Union countries have prohibited the inclusion of recycled vegetable oil from catering in animal feed. Used cooking oils from food manufacturing, however, as well as fresh or unused cooking oil, continue to be used in their animal feed.[71]
Shelf life[edit]
Due to their susceptibility to oxidation from the exposure to oxygen, heat and light, resulting in the formation of oxidation products, such as peroxides and hydroperoxides, plant oils rich in polyunsaturated fatty acids have a limited shelf-life.[72][73]
Product labeling[edit]
In Canada, palm oil is one of five vegetable oils, along with palm kernel oil, coconut oil, peanut oil, and cocoa butter, which must be specifically named in the list of ingredients for a food product.[74] Also, oils in Canadian food products which have been modified or hydrogenated must contain the word «modified» or «hydrogenated» when listed as an ingredient.[75] A mix of oils other than the aforementioned exceptions may simply be listed as «vegetable oil» in Canada; however, if the food product is a cooking oil, salad oil or table oil, the type of oil must be specified and listing «vegetable oil» as an ingredient is not acceptable.[74]
From December 2014, all food products produced in the European Union were legally required to indicate the specific vegetable oil used in their manufacture, following the introduction of the Food Information to Consumers Regulation.[76]
See also[edit]
- Algae culture
- Cholesterol
- Decorticator
- Deodorizer
- Essential oils
- Fatty acid
- Fatty acid methyl ester
- Food extrusion
- Fragrance oil
- Lipid
- List of macerated oils
- List of vegetable oils
- Neem
- Non-food crops
- Oleochemistry
- Soap
- Vernonia oil
- Vegetable oil recycling
Notes and references[edit]
- ^ Alfred Thomas (2002). «Fats and Fatty Oils». Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_173. ISBN 3527306730.
- ^ Parwez Saroj (September 2007). The Pearson Guide to the B.Sc. (Nursing) Entrance Examination. Pearson Education India. p. 109. ISBN 978-81-317-1338-9.
- ^ Robin Dand (1999). The International Cocoa Trade. Woodhead Publishing. p. 169. ISBN 1-85573-434-6.
- ^ a b c Ruth Schuster (December 17, 2014). «8,000-year old olive oil found in Galilee, earliest known in world», Haaretz. Retrieved December 17, 2014.
- ^ Ehud Galili et al., «Evidence for Earliest Olive-Oil Production in Submerged Settlements off the Carmel Coast, Israel», Journal of Archaeological Science 24:1141–1150 (1997); Pagnol, p. 19, says the 6th millennium in Jericho, but cites no source.
- ^ Harris, H. A. (2009). «Lubrication in Antiquity». Greece and Rome. 21 (1): 32–36. doi:10.1017/S0017383500021665. ISSN 0017-3835. S2CID 162746719.
- ^ «Blooming in Oil for Flavor» Cooks Illustrated
- ^ Linda McGraw (April 19, 2000). «Biodegradable Hydraulic Fluid Nears Market». USDA. Retrieved 2006-09-29.
- ^
«Cass Scenic Railroad, West Virginia». GWWCA. Retrieved 2011-11-01. - ^ «The Association of American Feed Control Officials (AAFCO)».
- ^ National Non-Food Crops Centre. GHG Benefits from Use of Vegetable Oils for Electricity, Heat, Transport, and Industrial Purposes, NNFCC 10-016 Archived 2016-03-05 at the Wayback Machine
- ^ Hossain, Amjad (2012). «Kalu». In Islam, Sirajul; Jamal, Ahmed A. (eds.). Banglapedia: National Encyclopedia of Bangladesh (Second ed.). Asiatic Society of Bangladesh.
- ^ Janet Bachmann. «Oilseed Processing for Small-Scale Producers». Retrieved 2006-07-31.
- ^ B.L. Axtell from research by R.M. Fairman (1992). «Illipe». Minor oil crops. FAO. Retrieved 2006-11-12.
- ^ Aziz, KMA (2012). «Ghani». In Islam, Sirajul; Jamal, Ahmed A. (eds.). Banglapedia: National Encyclopedia of Bangladesh (Second ed.). Asiatic Society of Bangladesh. A ghani is a traditional Indian oil press, driven by a horse or ox.
- ^ «Polyunsaturated Fats». Clark’s Nutrition. Retrieved March 13, 2019.
- ^ Eisenmenger, Michael; Dunford, Nurhan T.; Eller, Fred; Taylor, Scott; Martinez, Jose (2006). «Pilot-scale supercritical carbon dioxide extraction and fractionation of wheat germ oil». Journal of the American Oil Chemists’ Society. 83 (10): 863–868. doi:10.1007/s11746-006-5038-6. S2CID 59940212.
- ^ Trans Fat Task Force (June 2006). «TRANSforming the Food Supply (Appendix 9iii)». Archived from the original on February 25, 2007. Retrieved 2007-01-09. (Consultation on the health implications of alternatives to trans fatty acids: Summary of Responses from Experts)
- ^ «Final Determination Regarding Partially Hydrogenated Oils (Removing Trans Fat)». www.fda.gov. U.S. Food and Drug Administration. 20 February 2020. Retrieved 14 April 2021.
- ^ Feuge, R. O. «Vegetable Oils and Fats for Edible Use». usda.gov. Retrieved March 13, 2019.
Certain crude oils that contain minor amounts of impurities other than free fatty acids can be refined by a process known as steam refining. It is merely a high-temperature steam distillation under reduced pressure. The crude vegetable oil is heated to about 450° F. and maintained under a pressure of 0.25 inch of mercury or less while steam is passed through it. The steam strips the free fatty acids out of the oil. The proccss is used somewhat in Europe but not often in the United States.
- ^ Gupta, Monoj K. (2017). Practical guide to vegetable oil processing (Second ed.). Amsterdam. ISBN 978-1-63067-051-1. OCLC 974497799.
- ^ Lawrence Alan Johnson; Pamela J. White; Richard Galloway (2008). Soybeans : chemistry, production, processing, and utilization. Urbana, IL: AOCS Press. ISBN 978-0-12-804352-3. OCLC 491265615.
- ^ «Chapter 5 : Processing and refining edible oils». Food and Agriculture Organization of the United Nations. Retrieved 2021-07-04.
{{cite web}}
: CS1 maint: url-status (link) - ^ «CDC – NIOSH Pocket Guide to Chemical Hazards – Vegetable oil mist». www.cdc.gov. Retrieved 2015-11-27.
- ^ Malaysian Palm Oil Industry, palmoilworld.org
- ^ a b Oil Staple Crops Compared, gardeningplaces.com
- ^ a b Global oil yields: Have we got it seriously wrong? Archived 2016-01-31 at the Wayback Machine, Denis J. Murphy, August 2009, aocs.org
- ^ January 2009 (PDF). Oilseeds: World Market and Trade. Vol. FOP 1-09. USDA. 2009-01-12. Archived from the original (PDF) on 2013-03-09. Retrieved 2009-01-29., Table 03: Major Vegetable Oils: World Supply and Distribution at Oilseeds: World Markets and Trade Monthly Circular Archived 2010-10-18 at the Wayback Machine
- ^ a b c «US National Nutrient Database, Release 28». United States Department of Agriculture. May 2016. All values in this table are from this database unless otherwise cited or when italicized as the simple arithmetic sum of other component columns.
- ^ «Fats and fatty acids contents per 100 g (click for «more details»). Example: Avocado oil (user can search for other oils)». Nutritiondata.com, Conde Nast for the USDA National Nutrient Database, Standard Release 21. 2014. Retrieved 7 September 2017. Values from Nutritiondata.com (SR 21) may need to be reconciled with most recent release from the USDA SR 28 as of Sept 2017.
- ^ «USDA Specifications for Vegetable Oil Margarine Effective August 28, 1996» (PDF).
- ^ «Avocado oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ Feramuz Ozdemir; Ayhan Topuz (May 2003). «Changes in dry matter, oil content and fatty acids composition of avocado during harvesting time and post-harvesting ripening period» (PDF). Elsevier. Retrieved 15 January 2020.
- ^ Marie Wong; Cecilia Requejo-Jackman; Allan Woolf (April 2010). «What is unrefined, extra virgin cold-pressed avocado oil?». Aocs.org. The American Oil Chemists’ Society. Retrieved 26 December 2019.
- ^ «Brazil nut oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ a b c d e Katragadda, H. R.; Fullana, A. S.; Sidhu, S.; Carbonell-Barrachina, Á. A. (2010). «Emissions of volatile aldehydes from heated cooking oils». Food Chemistry. 120: 59–65. doi:10.1016/j.foodchem.2009.09.070.
- ^ «Canola oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Coconut oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Corn oil, industrial and retail, all purpose salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ a b c d e Wolke, Robert L. (May 16, 2007). «Where There’s Smoke, There’s a Fryer». The Washington Post. Retrieved March 5, 2011.
- ^ «Cottonseed oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Cottonseed oil, industrial, fully hydrogenated, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Linseed/Flaxseed oil, cold pressed, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ Garavaglia J, Markoski MM, Oliveira A, Marcadenti A (2016). «Grape Seed Oil Compounds: Biological and Chemical Actions for Health». Nutrition and Metabolic Insights. 9: 59–64. doi:10.4137/NMI.S32910. PMC 4988453. PMID 27559299.
- ^ Callaway J, Schwab U, Harvima I, Halonen P, Mykkänen O, Hyvönen P, Järvinen T (April 2005). «Efficacy of dietary hempseed oil in patients with atopic dermatitis». The Journal of Dermatological Treatment. 16 (2): 87–94. doi:10.1080/09546630510035832. PMID 16019622. S2CID 18445488.
- ^ Melina, Vesanto. «Smoke points of oils» (PDF). veghealth.com. The Vegetarian Health Institute.
- ^ «Olive oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Palm oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Palm oil, industrial, fully hydrogenated, filling fat, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Oil, peanut». FoodData Central. usda.gov.
- ^ Orthoefer, F. T. (2005). «Chapter 10: Rice Bran Oil». In Shahidi, F. (ed.). Bailey’s Industrial Oil and Fat Products. Vol. 2 (6 ed.). John Wiley & Sons, Inc. p. 465. doi:10.1002/047167849X. ISBN 978-0-471-38552-3.
- ^ «Rice bran oil». RITO Partnership. Retrieved 22 January 2021.
- ^ «Safflower oil, salad or cooking, high oleic, primary commerce, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Oil, sesame, salad or cooking». FoodData Central. fdc.nal.usda.gov. 1 April 2019.
- ^ «Soybean oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Soybean oil, salad or cooking, (partially hydrogenated), fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Walnut oil, fat composition, 100 g». US National Nutrient Database, United States Department of Agriculture.
- ^ «Smoke Point of Oils». Baseline of Health. Jonbarron.org.
- ^ «FoodData Central». fdc.nal.usda.gov.
- ^ «Expeller Pressed Method for Vegetable Oil Extraction». www.kmecomp.com. Retrieved 2020-05-28.
- ^ «British Colonial Policies and the Oil Palm Industry in the Niger Delta Region of Nigeria, 1900–1960» (PDF). African Study Monographs. 21 (1): 19–33. 2000. Archived (PDF) from the original on 16 January 2013.
- ^ Bellis, Mary. «The History of Soaps and Detergents». About.com.
In 1864, Caleb Johnson founded a soap company called B.J. Johnson Soap Co., in Milwaukee. In 1898, this company introduced a soap made of palm and olive oils called Palmolive.
- ^ Commercial Agriculture, the Slave Trade and Slavery in Atlantic Africa ISBN 978-1-847-01075-9 p. 22
- ^ «Soybean Car». Popular Research Topics. Benson Ford Research Center. Retrieved 2006-10-23.
- ^ Horstman, Barry M. (1999-05-21). «Philip W. Drackett: Earned profits, plaudits». The Cincinnati Post. E. W. Scripps Company. Archived from the original on 2005-12-05. Retrieved 2006-10-22.
- ^ «World Soy Oil Production». The Soybean Processors Association of India. Archived from the original on 2019-01-04. Retrieved 2019-01-04.
- ^ «Biodiesel Day». Days Of The Year. Retrieved 30 May 2015.
- ^ Knothe, G. «Historical Perspectives on Vegetable Oil-Based Diesel Fuels» (PDF). Inform, Vol. 12(11), pp. 1103–1107 (2001). Retrieved 2007-07-11.
- ^ Avril Group : Activity Report 2014, p. 58[full citation needed]
- ^ «Canola oil». Food and Drug Administration. Archived from the original on 2006-06-17. Retrieved 2006-07-31.
- ^ «Food and cooking oil waste». Food Standards Agency. GOV.UK. 22 May 2018.
- ^ H. Ramachandra Prabhu (2000). «Lipid peroxidation in culinary oils subjected to thermal stress». Indian Journal of Clinical Biochemistry. 15 (1): 1–5. doi:10.1007/BF02873539. PMC 3453543. PMID 23105229.
- ^ Tańska, M; Roszkowska, B; Skrajda, M; Dąbrowski, G (2016). «Commercial Cold Pressed Flaxseed Oils Quality and Oxidative Stability at the Beginning and the End of Their Shelf Life». Journal of Oleo Science. 65 (2): 111–21. doi:10.5650/jos.ess15243. PMID 26782307.
- ^ a b «Basic Labelling Requirements», Guide to Food Labelling and Advertising, Canadian Food Inspection Agency, 18 February 2014, retrieved 2015-04-08
- ^ «Common Name — Fats and Oils» (PDF), Labelling Requirements for Fats and Oils, Canadian Food Inspection Agency, retrieved 2015-04-08
- ^ «Regulation (EU) No 1169/2011 of the European Parliament and of the Council», Official Journal of the European Union, 2011-11-21
Further reading[edit]
- Gupta, Monoj K. (2007). Practical guide for vegetable oil processing. AOCS Press, Urbana, Illinois. ISBN 978-1-893997-90-5.
- Jee, Michael, ed. (2002). Oils and Fats Authentication. Blackwell Publishing, Oxford, England. ISBN 1-84127-330-9.
- Salunkhe, D.K., Chavan, J.K., Adsule, R.N. and Kadam, S.S. (1992). World Oilseeds – Chemistry, Technology, and Utilization. Van Nostrand Reinhold, New York. ISBN 0-442-00112-6.
{{cite book}}
: CS1 maint: multiple names: authors list (link)
Vegetable oils, or vegetable fats, are oils extracted from seeds or from other parts of fruits. Like animal fats, vegetable fats are mixtures of triglycerides.[1] Soybean oil, grape seed oil, and cocoa butter are examples of seed oils, or fats from seeds. Olive oil, palm oil, and rice bran oil are examples of fats from other parts of fruits. In common usage, vegetable oil may refer exclusively to vegetable fats which are liquid at room temperature.[2][3] Vegetable oils are usually edible.
Uses[edit]
In antiquity[edit]
Oils extracted from plants have been used since ancient times and in many cultures. Archaeological evidence shows that olives were turned into olive oil by 6000 BCE[4] and 4500 BCE in present-day Israel and Palestine.[5]
In addition to use as food, fats and oils (both vegetable and mineral) have long been used as fuel, typically in lamps which were a principal source of illumination in ancient times. Oils may have been used for lubrication, but there is no evidence for this. Vegetable oils were probably more valuable as food and lamp-oil;[citation needed] Babylonian mineral oil was known to be used as fuel, but there are no references to lubrication. Pliny the Elder reported that animal-derived fats such as lard were used to lubricate the axles of carts.[6]
Culinary[edit]
Many vegetable oils are consumed directly, or indirectly as ingredients in food – a role that they share with some animal fats, including butter, ghee, lard, and schmaltz. The oils serve a number of purposes in this role:
- Shortening – as in giving pastries a crumbly texture.
- Enriching – adding calories and satisfaction in consumption
- Texture – altering how ingredients combine, especially fats and starches
- Flavoring – examples include olive, sesame, or almond oil
- Flavor base – oils can also «carry» flavors of other ingredients, such as peppers,[7] since many flavors are due to chemicals that are soluble in oil.
Oils can be heated to temperatures significantly higher than the boiling point of water, 100 °C (212 °F), and used to fry foods. Oils for this purpose must have a high flash point. Such oils include both the major cooking oils – soybean, rapeseed, canola, sunflower, safflower, peanut, cottonseed, etc. – and tropical oils, such as coconut, palm, and rice bran. The latter are particularly valued in Asian cultures for high-temperature cooking, because of their unusually high flash points.
Industrial[edit]
Vegetable oils are used as an ingredient or component in many manufactured products.
Many vegetable oils are used to make soaps, skin products, candles, perfumes and other personal care and cosmetic products. Some oils are particularly suitable as drying oils, and are used in making paints and other wood treatment products. They are used in alkyd resin production. Dammar oil (a mixture of linseed oil and dammar resin), for example, is used almost exclusively in treating the hulls of wooden boats. Vegetable oils are increasingly being used in the electrical industry as insulators as vegetable oils are not toxic to the environment, biodegradable if spilled and have high flash and fire points. However, vegetable oils are less stable chemically, so they are generally used in systems where they are not exposed to oxygen, and they are more expensive than crude oil distillate. Synthetic tetraesters, which are similar to vegetable oils but with four fatty acid chains compared to the normal three found in a natural ester, are manufactured by Fischer esterification. Tetraesters generally have high stability to oxidation and have found use as engine lubricants. Vegetable oil is being used to produce biodegradable hydraulic fluid[8] and lubricant.[9]
One limiting factor in industrial uses of vegetable oils is that all such oils are susceptible to becoming rancid. Oils that are more stable, such as ben oil or mineral oil, are thus preferred for industrial uses. Castor oil has numerous industrial uses, owing to the presence of hydroxyl group on the fatty acid. Castor oil is a precursor to Nylon 11. Castor oil may also be reacted with epichlorohydrin to make a glycidyl ether which is used as a diluent and flexibilizer with epoxy resins.
Pet food additive[edit]
Vegetable oil is used in the production of some pet foods. AAFCO[10] defines vegetable oil in this context as the product of vegetable origin obtained by extracting the oil from seeds or fruits which are processed for edible purposes.
Fuel[edit]
Vegetable oils are also used to make biodiesel, which can be used like conventional diesel. Some vegetable oil blends are used in unmodified vehicles but straight vegetable oil, also known as pure plant oil, needs specially prepared vehicles which have a method of heating the oil to reduce its viscosity. The use of vegetable oils as alternative energy is growing[citation needed] and the availability of biodiesel around the world is increasing.[citation needed]
The NNFCC estimates that the total net greenhouse gas savings when using vegetable oils in place of fossil fuel-based alternatives for fuel production, range from 18 to 100%.[11]
Production[edit]
The production process of vegetable oil involves the removal of oil from plant components, typically seeds. This can be done via mechanical extraction using an oil mill or chemical extraction using a solvent. The extracted oil can then be purified and, if required, refined or chemically altered.
[edit]
Oils can be removed via mechanical extraction, termed «crushing» or «pressing.» This method is typically used to produce the more traditional oils (e.g., olive, coconut etc.), and it is preferred by most health-food customers in the United States and in Europe.[citation needed] There are several different types of mechanical extraction.[12] Expeller pressing extraction is common, though the screw press, ram press, and ghani (powered mortar and pestle) are also used. Oilseed presses are commonly used in developing countries, among people for whom other extraction methods would be prohibitively expensive; the ghani is primarily used in India.[13] The amount of oil extracted using these methods varies widely, as shown in the following table for extracting mowrah butter in India:[14]
Method | Percentage extracted |
---|---|
Ghani[15] | 20–30% |
Expellers | 34–37% |
Solvent | 40–43% |
[edit]
The processing of vegetable oil in commercial applications is commonly done by chemical extraction, using solvent extracts, which produces higher yields and is quicker and less expensive. The most common solvent is petroleum-derived hexane. This technique is used for most of the «newer» industrial oils such as soybean and corn oils. After extraction, the solvent is evaporated out by heating the mixture to about 300 °F (149 °C).[16]
Supercritical carbon dioxide can be used as a non-toxic alternative to other solvents.[17]
Hydrogenation[edit]
Unsaturated vegetable oils can be transformed through partial or complete hydrogenation into oils of higher melting point, some of which, such as vegetable shortening, will remain solid at room temperature.
Hydrogenating vegetable oil is done by raising a blend of vegetable oil and a metal catalyst, typically nickel, in near-vacuum to very high temperatures, and introducing hydrogen. This causes the carbon atoms of the oil to break double-bonds with other carbons. Each carbon atom becomes single-bonded to an individual hydrogen atom, and the double bond between carbons can no longer exist. A fully hydrogenated oil, also called a saturated fat, has had all of its double bonds converted into single bonds. If a polyunsaturated oil is left incompletely-hydrogenated (not all of the double bonds are reduced to single bonds), then it is a «partially hydrogenated oil» (PHO). An oil may be hydrogenated to increase resistance to rancidity (oxidation) or to change its physical characteristics. As the degree of saturation is raised by full or partial hydrogenation, the oil’s viscosity and melting point increase.
While full hydrogenation produces largely saturated fatty acids, partial hydrogenation results in the transformation of unsaturated cis fatty acids to unsaturated trans fatty acids in the oil mixture due to the heat used in hydrogenation. Partially hydrogenated oils and their trans fats have been linked to an increased risk of mortality from coronary heart disease,[18] among other increased health risks. These concerns have led to regulations mandating the removal of partially hydrogenated oils from food.[19]
Deodorization[edit]
In the processing of edible oils, the oil is heated under vacuum to near the smoke point or to about 450 °F (232 °C),[20] and water is introduced at the bottom of the oil. The water immediately is converted to steam, which bubbles through the oil, carrying with it any chemicals which are water-soluble. The steam sparging removes impurities that can impart unwanted flavors and odors to the oil. Deodorization is key to the manufacture of vegetable oils. Nearly all soybean, corn, and canola oils found on supermarket shelves go through a deodorization stage that removes trace amounts of odors and flavors, and lightens the color of the oil. However, the process commonly results in higher levels of trans fatty acids and distillation of the oil’s natural compounds.[21][22][23]
Occupational exposure[edit]
People can breathe in vegetable oil mist in the workplace. The U.S. Occupational Safety and Health Administration (OSHA) has set the legal limit (permissible exposure limit) for vegetable oil mist exposure in the workplace as 15 mg/m3 total exposure and 5 mg/m3 respiratory exposure over an 8-hour workday. The U.S. National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 10 mg/m3 total exposure and 5 mg/m3 respiratory exposure over an 8-hour workday.[24]
Yield[edit]
Typical productivity of some oil crops, measured in tons (t) of oil produced per hectare (ha) of land per year (yr). Oil palm is by far the highest yielding crop, capable of producing about 4 tons of palm oil per hectare per year.
Crop | Yield (t/ha/yr) |
---|---|
Palm oil [25] | 4.0 |
Coconut oil [26] | 1.4 |
Canola oil [27] | 1.4 |
Soybean oil [27] | 0.6 |
Sunflower oil [26] | 0.6 |
Particular oils[edit]
The following triglyceride vegetable oils account for almost all worldwide production, by volume. All are used as both cooking oils and as SVO or to make biodiesel. According to the USDA, the total world consumption of major vegetable oils in 2007/08 was:[28]
Oil source | World consumption (million metric tons) |
Notes |
---|---|---|
Palm | 41.31 | The most widely produced tropical oil, also used to make biofuel |
Soybean | 41.28 | One of the most widely consumed cooking oils |
Rapeseed | 18.24 | One of the most widely used cooking oils, also used as fuel. Canola is a variety (cultivar) of rapeseed. |
Sunflower seed | 9.91 | A common cooking oil, also used to make biodiesel |
Peanut | 4.82 | Mild-flavored cooking oil |
Cottonseed | 4.99 | A major food oil, often used in industrial food processing |
Palm kernel | 4.85 | From the seed of the African palm tree |
Coconut | 3.48 | Used in cooking, cosmetics and soaps |
Olive | 2.84 | Used in cooking, cosmetics, soaps and as a fuel for traditional oil lamps |
Note that these figures include industrial and animal feed use. The majority of European rapeseed oil production is used to produce biodiesel, or used directly as fuel in diesel cars which may require modification to heat the oil to reduce its higher viscosity.
Other significant oils include:
- Corn oil, one of the most common cooking oils, is used for cooking oil, salad dressing, margarine, mayonnaise, prepared goods like spaghetti sauce and baking mixes, and to fry prepared foods like potato chips and French fries.
- Grape seed oil, used in cooking and cosmetics
- Hazelnut oil and other nut oils
- Linseed oil, from flax seeds
- Rice bran oil, from rice grains
- Safflower oil, a flavorless and colorless cooking oil
- Sesame oil, used as a cooking oil, and as a massage oil, particularly in India
- Açaí palm oil, used in culinary and cosmetics
- Jambú oil, is extracted from the flowers, leaves and stem from jambu (Acmella oleracea), contains spilanthol
- Graviola oil, derived from Annona muricata
- Tucumã oil, from Astrocaryum aculeatum is used to manufacture soap.
- Brazil nut oil, culinary and cosmetics use
- Carapa oil, pharmaceutical use and anti-mosquito candle
- Buriti oil, from Mauritia flexuosa, used in cosmetics (skin and hair care)
- Passion fruit oil, derived from Passiflora edulis, has varied applications in cosmetics manufacturing and for uses as a human or animal food.
- Pracaxi oil, obtained from Pentaclethra macroloba, cosmetics use
- Solarium oil, derived from chloroplasts, various applications in cooking
Composition of fats[edit]
Properties of vegetable oils[29][30]
The nutritional values are expressed as percent (%) by mass of total fat. | |||||||||
Type | Processing treatment[31] |
Saturated fatty acids |
Monounsaturated fatty acids |
Polyunsaturated fatty acids |
Smoke point | ||||
---|---|---|---|---|---|---|---|---|---|
Total[29] | Oleic acid (ω-9) |
Total[29] | α-Linolenic acid (ω-3) |
Linoleic acid (ω-6) |
ω-6:3 ratio |
||||
Avocado[32] | 11.6 | 70.6 | 52–66[33] | 13.5 | 1 | 12.5 | 12.5:1 | 250 °C (482 °F)[34] | |
Brazil nut[35] | 24.8 | 32.7 | 31.3 | 42.0 | 0.1 | 41.9 | 419:1 | 208 °C (406 °F)[36] | |
Canola[37] | 7.4 | 63.3 | 61.8 | 28.1 | 9.1 | 18.6 | 2:1 | 238 °C (460 °F)[36] | |
Coconut[38] | 82.5 | 6.3 | 6 | 1.7 | 175 °C (347 °F)[36] | ||||
Corn[39] | 12.9 | 27.6 | 27.3 | 54.7 | 1 | 58 | 58:1 | 232 °C (450 °F)[40] | |
Cottonseed[41] | 25.9 | 17.8 | 19 | 51.9 | 1 | 54 | 54:1 | 216 °C (420 °F)[40] | |
Cottonseed[42] | hydrogenated | 93.6 | 1.5 | 0.6 | 0.2 | 0.3 | 1.5:1 | ||
Flaxseed/linseed[43] | 9.0 | 18.4 | 18 | 67.8 | 53 | 13 | 0.2:1 | 107 °C (225 °F) | |
Grape seed | 10.5 | 14.3 | 14.3 | 74.7 | – | 74.7 | very high | 216 °C (421 °F)[44] | |
Hemp seed[45] | 7.0 | 9.0 | 9.0 | 82.0 | 22.0 | 54.0 | 2.5:1 | 166 °C (330 °F)[46] | |
Olive[47] | 13.8 | 73.0 | 71.3 | 10.5 | 0.7 | 9.8 | 14:1 | 193 °C (380 °F)[36] | |
Palm[48] | 49.3 | 37.0 | 40 | 9.3 | 0.2 | 9.1 | 45.5:1 | 235 °C (455 °F) | |
Palm[49] | hydrogenated | 88.2 | 5.7 | 0 | |||||
Peanut[50] | 16.2 | 57.1 | 55.4 | 19.9 | 0.318 | 19.6 | 61.6:1 | 232 °C (450 °F)[40] | |
Rice bran oil | 25 | 38.4 | 38.4 | 36.6 | 2.2 | 34.4[51] | 15.6 | 232 °C (450 °F)[52] | |
High-oleic safflower oil[53] | 7.5 | 75.2 | 75.2 | 12.8 | 0 | 12.8 | very high | 212 °C (414 °F)[36] | |
Sesame[54] | 14.2 | 39.7 | 39.3 | 41.7 | 0.3 | 41.3 | 138:1 | ||
Soybean[55] | 15.6 | 22.8 | 22.6 | 57.7 | 7 | 51 | 7.3:1 | 238 °C (460 °F)[40] | |
Soybean[56] | partially hydrogenated | 14.9 | 43.0 | 42.5 | 37.6 | 2.6 | 34.9 | 13.4:1 | |
Walnut oil[57] | unrefined | 9.1 | 22.8 | 22.2 | 63.3 | 10.4 | 52.9 | 5:1 | 160 °C (320 °F)[58] |
Sunflower[59] | 8.99 | 63.4 | 62.9 | 20.7 | 0.16 | 20.5 | 128:1 | 227 °C (440 °F)[40] |
Seed oil[edit]
Seed oils are vegetable oils obtained from the seed (endosperm) of some plants, rather than the fruit (pericarp). Most vegetable oils are seed oils. Examples are sunflower, corn, and sesame oils.
Pre-pressing[edit]
Extracting the oils first by expeller or cold pressing methods, then solvent expelling the rest of the oils from the leftover matter. This is a method used by larger capacity oil mills. As the energy consumption of the mechanical press increases as more oil is released, it is more efficient to extract the rest of the oil (past around 60%) by solvent extraction.[60]
History[edit]
Such oils have been part of human culture for millennia.[4] Oils such as poppy seed, rapeseed, linseed, almond oil, sesame seed, safflower, and cottonseed were variously used since at least the Bronze Age in the Middle East.[4] Vegetable oils have been used for lighting fuel, cooking, medicine and lubrication.
Palm oil has long been recognized in West and Central African countries, and European merchants trading with West Africa occasionally purchased palm oil for use as a cooking oil in Europe and it became highly sought-after commodity by British traders for use as an industrial lubricant for machinery during Britain’s Industrial Revolution.[61] Palm oil formed the basis of soap products, such as Lever Brothers’ (now Unilever) «Sunlight», and
B. J. Johnson Company’s (now Colgate-Palmolive) «Palmolive»,[62] and by around 1870, palm oil constituted the primary export of some West African countries.[63]
In 1780 Carl Wilhelm Scheele demonstrated that fats were derived from glycerol. Thirty years later Michel Eugène Chevreul deduced that these fats were esters of fatty acids and glycerol. Wilhelm Normann, a German chemist introduced the hydrogenation of liquid fats in 1901, creating what later became known as trans fats, leading to the development of the global production of margarine and vegetable shortening.
In the USA cottonseed oil was developed, and marketed by Procter & Gamble as a creamed shortening – Crisco – as early as 1911. Ginning mills were happy to have someone haul away the cotton seeds. The extracted oil was refined and partially hydrogenated to give a solid at room temperature and thus mimic natural lard, and canned under nitrogen gas. Compared to the rendered lard Procter & Gamble was already selling to consumers, Crisco was cheaper, easier to stir into a recipe, and could be stored at room temperature for two years without turning rancid.
Soybeans are protein-rich, and the medium viscosity oil rendered from them was high in polyunsaturates. Henry Ford established a soybean research laboratory, developed soybean plastics and a soy-based synthetic wool, and built a car «almost entirely» out of soybeans.[64] Roger Drackett had a successful new product with Windex, but he invested heavily in soybean research, seeing it as a smart investment.[65] By the 1950s and 1960s, soybean oil had become the most popular vegetable oil in the US; today it is second only to palm oil. In 2018–2019, world production was at 57.4 MT with the leading producers including China (16.6 MT), US (10.9 MT), Argentina (8.4 MT), Brazil (8.2 MT), and EU (3.2 MT).[66]
The early 20th century also saw the start of the use of vegetable oil as a fuel in diesel engines and in heating oil burners. Rudolf Diesel designed his engine to run on vegetable oil. The idea, he hoped, would make his engines more attractive to farmers having a source of fuel readily available. Diesel’s first engine ran on its own power for the first time in Augsburg, Germany, on 10 August 1893 on nothing but peanut oil. In remembrance of this event, 10 August has been declared «International Biodiesel Day».[67] The first patent on Biodiesel was granted in 1937.[68] Periodic petroleum shortages spurred research into vegetable oil as a diesel substitute during the 1930s and 1940s, and again in the 1970s and early 1980s when straight vegetable oil enjoyed its highest level of scientific interest. The 1970s also saw the formation of the first commercial enterprise to allow consumers to run straight vegetable oil in their vehicles. However, biodiesel, produced from oils or fats using transesterification is more widely used. It is Led by Brazil, many countries built biodiesel plants during the 1990s, and it is now widely available for use in motor vehicles, and is the most common biofuel in Europe today. In France, biodiesel is incorporated at a rate of 8% in the fuel used by all French diesel vehicles.[69]
In the mid-1970s, Canadian researchers developed a low-erucic-acid rapeseed cultivar. Because the word «rape» was not considered optimal for marketing, they coined the name «canola» (from «Canada Oil low acid»). The U.S. Food and Drug Administration approved use of the canola name in January 1985,[70] and U.S. farmers started planting large areas that spring. Canola oil is lower in saturated fats, and higher in monounsaturates. Canola is very thin (unlike corn oil) and flavorless (unlike olive oil), so it largely succeeds by displacing soy oil, just as soy oil largely succeeded by displacing cottonseed oil.
Used oil[edit]
A large quantity of used vegetable oil is produced and recycled, mainly from industrial deep fryers in potato processing plants, snack food factories and fast food restaurants.
Recycled oil has numerous uses, including use as a direct fuel, as well as in the production of biodiesel, livestock feed, pet food, soap, detergent, cosmetics, and industrial chemicals.
Since 2002, an increasing number of European Union countries have prohibited the inclusion of recycled vegetable oil from catering in animal feed. Used cooking oils from food manufacturing, however, as well as fresh or unused cooking oil, continue to be used in their animal feed.[71]
Shelf life[edit]
Due to their susceptibility to oxidation from the exposure to oxygen, heat and light, resulting in the formation of oxidation products, such as peroxides and hydroperoxides, plant oils rich in polyunsaturated fatty acids have a limited shelf-life.[72][73]
Product labeling[edit]
In Canada, palm oil is one of five vegetable oils, along with palm kernel oil, coconut oil, peanut oil, and cocoa butter, which must be specifically named in the list of ingredients for a food product.[74] Also, oils in Canadian food products which have been modified or hydrogenated must contain the word «modified» or «hydrogenated» when listed as an ingredient.[75] A mix of oils other than the aforementioned exceptions may simply be listed as «vegetable oil» in Canada; however, if the food product is a cooking oil, salad oil or table oil, the type of oil must be specified and listing «vegetable oil» as an ingredient is not acceptable.[74]
From December 2014, all food products produced in the European Union were legally required to indicate the specific vegetable oil used in their manufacture, following the introduction of the Food Information to Consumers Regulation.[76]
See also[edit]
- Algae culture
- Cholesterol
- Decorticator
- Deodorizer
- Essential oils
- Fatty acid
- Fatty acid methyl ester
- Food extrusion
- Fragrance oil
- Lipid
- List of macerated oils
- List of vegetable oils
- Neem
- Non-food crops
- Oleochemistry
- Soap
- Vernonia oil
- Vegetable oil recycling
Notes and references[edit]
- ^ Alfred Thomas (2002). «Fats and Fatty Oils». Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_173. ISBN 3527306730.
- ^ Parwez Saroj (September 2007). The Pearson Guide to the B.Sc. (Nursing) Entrance Examination. Pearson Education India. p. 109. ISBN 978-81-317-1338-9.
- ^ Robin Dand (1999). The International Cocoa Trade. Woodhead Publishing. p. 169. ISBN 1-85573-434-6.
- ^ a b c Ruth Schuster (December 17, 2014). «8,000-year old olive oil found in Galilee, earliest known in world», Haaretz. Retrieved December 17, 2014.
- ^ Ehud Galili et al., «Evidence for Earliest Olive-Oil Production in Submerged Settlements off the Carmel Coast, Israel», Journal of Archaeological Science 24:1141–1150 (1997); Pagnol, p. 19, says the 6th millennium in Jericho, but cites no source.
- ^ Harris, H. A. (2009). «Lubrication in Antiquity». Greece and Rome. 21 (1): 32–36. doi:10.1017/S0017383500021665. ISSN 0017-3835. S2CID 162746719.
- ^ «Blooming in Oil for Flavor» Cooks Illustrated
- ^ Linda McGraw (April 19, 2000). «Biodegradable Hydraulic Fluid Nears Market». USDA. Retrieved 2006-09-29.
- ^
«Cass Scenic Railroad, West Virginia». GWWCA. Retrieved 2011-11-01. - ^ «The Association of American Feed Control Officials (AAFCO)».
- ^ National Non-Food Crops Centre. GHG Benefits from Use of Vegetable Oils for Electricity, Heat, Transport, and Industrial Purposes, NNFCC 10-016 Archived 2016-03-05 at the Wayback Machine
- ^ Hossain, Amjad (2012). «Kalu». In Islam, Sirajul; Jamal, Ahmed A. (eds.). Banglapedia: National Encyclopedia of Bangladesh (Second ed.). Asiatic Society of Bangladesh.
- ^ Janet Bachmann. «Oilseed Processing for Small-Scale Producers». Retrieved 2006-07-31.
- ^ B.L. Axtell from research by R.M. Fairman (1992). «Illipe». Minor oil crops. FAO. Retrieved 2006-11-12.
- ^ Aziz, KMA (2012). «Ghani». In Islam, Sirajul; Jamal, Ahmed A. (eds.). Banglapedia: National Encyclopedia of Bangladesh (Second ed.). Asiatic Society of Bangladesh. A ghani is a traditional Indian oil press, driven by a horse or ox.
- ^ «Polyunsaturated Fats». Clark’s Nutrition. Retrieved March 13, 2019.
- ^ Eisenmenger, Michael; Dunford, Nurhan T.; Eller, Fred; Taylor, Scott; Martinez, Jose (2006). «Pilot-scale supercritical carbon dioxide extraction and fractionation of wheat germ oil». Journal of the American Oil Chemists’ Society. 83 (10): 863–868. doi:10.1007/s11746-006-5038-6. S2CID 59940212.
- ^ Trans Fat Task Force (June 2006). «TRANSforming the Food Supply (Appendix 9iii)». Archived from the original on February 25, 2007. Retrieved 2007-01-09. (Consultation on the health implications of alternatives to trans fatty acids: Summary of Responses from Experts)
- ^ «Final Determination Regarding Partially Hydrogenated Oils (Removing Trans Fat)». www.fda.gov. U.S. Food and Drug Administration. 20 February 2020. Retrieved 14 April 2021.
- ^ Feuge, R. O. «Vegetable Oils and Fats for Edible Use». usda.gov. Retrieved March 13, 2019.
Certain crude oils that contain minor amounts of impurities other than free fatty acids can be refined by a process known as steam refining. It is merely a high-temperature steam distillation under reduced pressure. The crude vegetable oil is heated to about 450° F. and maintained under a pressure of 0.25 inch of mercury or less while steam is passed through it. The steam strips the free fatty acids out of the oil. The proccss is used somewhat in Europe but not often in the United States.
- ^ Gupta, Monoj K. (2017). Practical guide to vegetable oil processing (Second ed.). Amsterdam. ISBN 978-1-63067-051-1. OCLC 974497799.
- ^ Lawrence Alan Johnson; Pamela J. White; Richard Galloway (2008). Soybeans : chemistry, production, processing, and utilization. Urbana, IL: AOCS Press. ISBN 978-0-12-804352-3. OCLC 491265615.
- ^ «Chapter 5 : Processing and refining edible oils». Food and Agriculture Organization of the United Nations. Retrieved 2021-07-04.
{{cite web}}
: CS1 maint: url-status (link) - ^ «CDC – NIOSH Pocket Guide to Chemical Hazards – Vegetable oil mist». www.cdc.gov. Retrieved 2015-11-27.
- ^ Malaysian Palm Oil Industry, palmoilworld.org
- ^ a b Oil Staple Crops Compared, gardeningplaces.com
- ^ a b Global oil yields: Have we got it seriously wrong? Archived 2016-01-31 at the Wayback Machine, Denis J. Murphy, August 2009, aocs.org
- ^ January 2009 (PDF). Oilseeds: World Market and Trade. Vol. FOP 1-09. USDA. 2009-01-12. Archived from the original (PDF) on 2013-03-09. Retrieved 2009-01-29., Table 03: Major Vegetable Oils: World Supply and Distribution at Oilseeds: World Markets and Trade Monthly Circular Archived 2010-10-18 at the Wayback Machine
- ^ a b c «US National Nutrient Database, Release 28». United States Department of Agriculture. May 2016. All values in this table are from this database unless otherwise cited or when italicized as the simple arithmetic sum of other component columns.
- ^ «Fats and fatty acids contents per 100 g (click for «more details»). Example: Avocado oil (user can search for other oils)». Nutritiondata.com, Conde Nast for the USDA National Nutrient Database, Standard Release 21. 2014. Retrieved 7 September 2017. Values from Nutritiondata.com (SR 21) may need to be reconciled with most recent release from the USDA SR 28 as of Sept 2017.
- ^ «USDA Specifications for Vegetable Oil Margarine Effective August 28, 1996» (PDF).
- ^ «Avocado oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ Feramuz Ozdemir; Ayhan Topuz (May 2003). «Changes in dry matter, oil content and fatty acids composition of avocado during harvesting time and post-harvesting ripening period» (PDF). Elsevier. Retrieved 15 January 2020.
- ^ Marie Wong; Cecilia Requejo-Jackman; Allan Woolf (April 2010). «What is unrefined, extra virgin cold-pressed avocado oil?». Aocs.org. The American Oil Chemists’ Society. Retrieved 26 December 2019.
- ^ «Brazil nut oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ a b c d e Katragadda, H. R.; Fullana, A. S.; Sidhu, S.; Carbonell-Barrachina, Á. A. (2010). «Emissions of volatile aldehydes from heated cooking oils». Food Chemistry. 120: 59–65. doi:10.1016/j.foodchem.2009.09.070.
- ^ «Canola oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Coconut oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Corn oil, industrial and retail, all purpose salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ a b c d e Wolke, Robert L. (May 16, 2007). «Where There’s Smoke, There’s a Fryer». The Washington Post. Retrieved March 5, 2011.
- ^ «Cottonseed oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Cottonseed oil, industrial, fully hydrogenated, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Linseed/Flaxseed oil, cold pressed, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ Garavaglia J, Markoski MM, Oliveira A, Marcadenti A (2016). «Grape Seed Oil Compounds: Biological and Chemical Actions for Health». Nutrition and Metabolic Insights. 9: 59–64. doi:10.4137/NMI.S32910. PMC 4988453. PMID 27559299.
- ^ Callaway J, Schwab U, Harvima I, Halonen P, Mykkänen O, Hyvönen P, Järvinen T (April 2005). «Efficacy of dietary hempseed oil in patients with atopic dermatitis». The Journal of Dermatological Treatment. 16 (2): 87–94. doi:10.1080/09546630510035832. PMID 16019622. S2CID 18445488.
- ^ Melina, Vesanto. «Smoke points of oils» (PDF). veghealth.com. The Vegetarian Health Institute.
- ^ «Olive oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Palm oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Palm oil, industrial, fully hydrogenated, filling fat, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Oil, peanut». FoodData Central. usda.gov.
- ^ Orthoefer, F. T. (2005). «Chapter 10: Rice Bran Oil». In Shahidi, F. (ed.). Bailey’s Industrial Oil and Fat Products. Vol. 2 (6 ed.). John Wiley & Sons, Inc. p. 465. doi:10.1002/047167849X. ISBN 978-0-471-38552-3.
- ^ «Rice bran oil». RITO Partnership. Retrieved 22 January 2021.
- ^ «Safflower oil, salad or cooking, high oleic, primary commerce, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Oil, sesame, salad or cooking». FoodData Central. fdc.nal.usda.gov. 1 April 2019.
- ^ «Soybean oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Soybean oil, salad or cooking, (partially hydrogenated), fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Walnut oil, fat composition, 100 g». US National Nutrient Database, United States Department of Agriculture.
- ^ «Smoke Point of Oils». Baseline of Health. Jonbarron.org.
- ^ «FoodData Central». fdc.nal.usda.gov.
- ^ «Expeller Pressed Method for Vegetable Oil Extraction». www.kmecomp.com. Retrieved 2020-05-28.
- ^ «British Colonial Policies and the Oil Palm Industry in the Niger Delta Region of Nigeria, 1900–1960» (PDF). African Study Monographs. 21 (1): 19–33. 2000. Archived (PDF) from the original on 16 January 2013.
- ^ Bellis, Mary. «The History of Soaps and Detergents». About.com.
In 1864, Caleb Johnson founded a soap company called B.J. Johnson Soap Co., in Milwaukee. In 1898, this company introduced a soap made of palm and olive oils called Palmolive.
- ^ Commercial Agriculture, the Slave Trade and Slavery in Atlantic Africa ISBN 978-1-847-01075-9 p. 22
- ^ «Soybean Car». Popular Research Topics. Benson Ford Research Center. Retrieved 2006-10-23.
- ^ Horstman, Barry M. (1999-05-21). «Philip W. Drackett: Earned profits, plaudits». The Cincinnati Post. E. W. Scripps Company. Archived from the original on 2005-12-05. Retrieved 2006-10-22.
- ^ «World Soy Oil Production». The Soybean Processors Association of India. Archived from the original on 2019-01-04. Retrieved 2019-01-04.
- ^ «Biodiesel Day». Days Of The Year. Retrieved 30 May 2015.
- ^ Knothe, G. «Historical Perspectives on Vegetable Oil-Based Diesel Fuels» (PDF). Inform, Vol. 12(11), pp. 1103–1107 (2001). Retrieved 2007-07-11.
- ^ Avril Group : Activity Report 2014, p. 58[full citation needed]
- ^ «Canola oil». Food and Drug Administration. Archived from the original on 2006-06-17. Retrieved 2006-07-31.
- ^ «Food and cooking oil waste». Food Standards Agency. GOV.UK. 22 May 2018.
- ^ H. Ramachandra Prabhu (2000). «Lipid peroxidation in culinary oils subjected to thermal stress». Indian Journal of Clinical Biochemistry. 15 (1): 1–5. doi:10.1007/BF02873539. PMC 3453543. PMID 23105229.
- ^ Tańska, M; Roszkowska, B; Skrajda, M; Dąbrowski, G (2016). «Commercial Cold Pressed Flaxseed Oils Quality and Oxidative Stability at the Beginning and the End of Their Shelf Life». Journal of Oleo Science. 65 (2): 111–21. doi:10.5650/jos.ess15243. PMID 26782307.
- ^ a b «Basic Labelling Requirements», Guide to Food Labelling and Advertising, Canadian Food Inspection Agency, 18 February 2014, retrieved 2015-04-08
- ^ «Common Name — Fats and Oils» (PDF), Labelling Requirements for Fats and Oils, Canadian Food Inspection Agency, retrieved 2015-04-08
- ^ «Regulation (EU) No 1169/2011 of the European Parliament and of the Council», Official Journal of the European Union, 2011-11-21
Further reading[edit]
- Gupta, Monoj K. (2007). Practical guide for vegetable oil processing. AOCS Press, Urbana, Illinois. ISBN 978-1-893997-90-5.
- Jee, Michael, ed. (2002). Oils and Fats Authentication. Blackwell Publishing, Oxford, England. ISBN 1-84127-330-9.
- Salunkhe, D.K., Chavan, J.K., Adsule, R.N. and Kadam, S.S. (1992). World Oilseeds – Chemistry, Technology, and Utilization. Van Nostrand Reinhold, New York. ISBN 0-442-00112-6.
{{cite book}}
: CS1 maint: multiple names: authors list (link)
подсолнечное масло
- подсолнечное масло
- подсо́лнечное ма́сло
растительное жирное масло, получаемое из семян подсолнечника. Используется в пищу, для производства маргарина, консервов, а также лаков и мыл.
* * *
ПОДСОЛНЕЧНОЕ МАСЛО
ПОДСО́ЛНЕЧНОЕ МА́СЛО, растительное жирное масло, получаемое из семян подсолнечника. Используется в пищу, для производства маргарина, консервов, а также лаков и мыл.
Энциклопедический словарь.
2009.
Смотреть что такое «подсолнечное масло» в других словарях:
-
Подсолнечное масло — Подсолнечное масло … Википедия
-
ПОДСОЛНЕЧНОЕ МАСЛО — растительное жирное масло, получаемое из семян подсолнечника. Используется в пищу, для производства маргарина, консервов, а также лаков и мыл … Большой Энциклопедический словарь
-
подсолнечное масло — Растительное масло, извлекаемое из семян подсолнечника. [ГОСТ 21314 75] Тематики масла растительные … Справочник технического переводчика
-
Подсолнечное масло — Тип блюда: Категория: Рецепт приготовления: В текущей категории (Абрикосы): | | | | | | | | | | | | | | | | | | | | … Энциклопедия кулинарных рецептов
-
Подсолнечное масло — Это масло получают из семян подсолнечника (Helianthus annuus), оно имеет светлый золотисто желтый цвет. Используется как салатное масло, в производстве маргарина и заменителей лярда. Подсолнечное масло является полувысыхающим, что определяет его… … Официальная терминология
-
подсолнечное масло — saulėgrąžų aliejus statusas T sritis chemija apibrėžtis Iš saulėgrąžų sėklų spaudžiamas aliejus. atitikmenys: angl. sunflower oil rus. подсолнечное масло … Chemijos terminų aiškinamasis žodynas
-
Подсолнечное масло — масло растительное жирное, получаемое из семян Подсолнечника. Сырое П. м. имеет приятные запах и вкус. Плотность при 10 °С 920 927 кг/м3, температура застывания от 16 до 19 °С, кинематическая вязкость при 20 °С 60,6․10 6 м2/сек. … … Большая советская энциклопедия
-
Подсолнечное масло — см. Масла жирные, Маслобойные производства … Энциклопедический словарь Ф.А. Брокгауза и И.А. Ефрона
-
ПОДСОЛНЕЧНОЕ МАСЛО — светло желтая жидкость с приятным запахом; т. заст. от 180C до 190C; 0,924 0,927; 1,474 1,478; h 54,6 59,8 мПа … Химическая энциклопедия
-
Масло камелии — (восточное оливковое масло) растительное масло высокой вязкости, получаемое прессованием из богатых маслом семян различных видов камелии. Масло камелии производится и используется в основном в Китае, Вьетнаме и Японии. Содержание … Википедия
Unrefined sunflower oil with sunflower inflorescence
Refined high-oleic sunflower oil
Sunflower oil is the non-volatile oil pressed from the seeds of the sunflower (Helianthus annuus). Sunflower oil is commonly used in food as a frying oil, and in cosmetic formulations as an emollient.
Sunflower oil is primarily composed of linoleic acid, a polyunsaturated fat, and oleic acid, a monounsaturated fat. Through selective breeding and manufacturing processes, oils of differing proportions of the fatty acids are produced.[1] The expressed oil has a neutral taste profile.[2] The oil contains a large amount of vitamin E.[2]
As of 2017, genome analysis[3] and development of hybrid sunflowers to increase oil production are under development to meet greater consumer demand for sunflower oil and its commercial varieties.[4][5]
In 2018, Ukraine and Russia together accounted for 53% of the world’s production of sunflower oil.
Composition[edit]
Sunflower oil is mainly a triglyceride.[6] The British Pharmacopoeia lists the following profile:[7]
- Palmitic acid (saturated): 5%
- Stearic acid (saturated): 6%
- Oleic acid (monounsaturated omega-9): 30%
- Linoleic acid (polyunsaturated omega-6): 59%
Four types of sunflower oils with differing concentrations of fatty acids are produced through plant breeding and industrial processing: high-linoleic, high-oleic, mid-oleic, and high-stearic combined with high-oleic.[1][2]
- High-linoleic, 69% linoleic acid
- High-oleic, 82% oleic acid
- Mid-oleic, 65% oleic acid
- High-stearic with high-oleic, 18% stearic acid and 72% oleic acid[2]
Sunflower oil production – 2019 | |
---|---|
Country | (millions of tonnes) |
5.84 | |
5.42 | |
1.41 | |
1.10 | |
0.69 | |
0.53 | |
0.53 | |
0.52 | |
0.49 | |
0.32 | |
World | 20.29 |
Source: FAOSTAT of the United Nations[8] |
In an analysis of the sunflower genome to reveal plant metabolism producing its oil, phytosterols were identified,[3] as confirmed in another analysis of sunflower oil components, including polyphenols, squalene, and terpenoids.[9]
Production[edit]
Sunflower oil in the Silpo store in Kyiv, Ukraine. August 2021.
In 2018, world production of sunflower oil was 18 million tonnes, led by Ukraine and Russia as the leading producers accounting together for 53% of the world total.[8]
In 2022, there is a global shortage of sunflower oil due to the 2022 Russian invasion of Ukraine which has led to over 50% drop in the availability of sunflower oil. Due to the shortages many brands are reforming their recipes by switching to rapeseed oil to allow the production of their products to continue.
Nutrition[edit]
Nutritional value per 100 g (3.5 oz) | |
---|---|
Energy | 3,699 kJ (884 kcal) |
Carbohydrates |
0 g |
Fat |
100 g |
Saturated | 9.748 g |
Monounsaturated | 83.594 g |
Polyunsaturated | 3.798 g |
Protein |
0 g |
Vitamins | Quantity
%DV† |
Vitamin E |
274% 41.08 mg |
Vitamin K |
5% 5.4 μg |
|
|
†Percentages are roughly approximated using US recommendations for adults. Source: USDA FoodData Central |
Nutritional value per 100 g (3.5 oz) | |
---|---|
Energy | 3,699 kJ (884 kcal) |
Carbohydrates |
0 g |
Fat |
100 g |
Saturated | 10.3 g |
Monounsaturated | 19.5 g |
Polyunsaturated | 65.7 g |
Protein |
0 g |
Vitamins | Quantity
%DV† |
Vitamin E |
274% 41.08 mg |
Vitamin K |
5% 5.4 μg |
|
|
†Percentages are roughly approximated using US recommendations for adults. Source: USDA FoodData Central |
Nutritional value per 100 g (3.5 oz) | |
---|---|
Energy | 3,699 kJ (884 kcal) |
Carbohydrates |
0 g |
Fat |
100 g |
Saturated | 9.009 g |
Monounsaturated | 57.344 g |
Polyunsaturated | 28.962 g |
Protein |
0 g |
Vitamins | Quantity
%DV† |
Vitamin E |
274% 41.08 mg |
Vitamin K |
5% 5.4 μg |
|
|
†Percentages are roughly approximated using US recommendations for adults. Source: USDA FoodData Central |
Several varieties of sunflower oil seeds have been developed by standard plant breeding methods, mainly to vary the amounts of oleic acid and linoleic acid which, respectively, are the predominant monounsaturated and polyunsaturated fats in sunflower oil.[10] Sunflower oil is a rich source of vitamin E (tables).
Physical properties[edit]
Sunflower oil is liquid at room temperature. The refined oil is clear and slightly amber-colored with a slightly fatty odour.
Smoke point (refined) | 232 °C | 450 °F[11] |
Smoke point (unrefined) | 107 °C | 225 °F[11] |
Density (25 °C) | 918.8 kg/m3[12] | |
Refractive index (25 °C) | ≈1.4735[12] | |
Saponification value | 188-194 | |
Iodine value | 120-145 | |
Unsaponifiable matter | 1.5-2.0% | |
Viscosity (25 °C), unrefined | 0.04914
kg/(m*s)[13] |
Preparation and storage[edit]
Because sunflower oil is primarily composed of less-stable polyunsaturated and monounsaturated fatty acids, it can be particularly susceptible to degradation by heat, air, and light, which trigger and accelerate oxidation. Keeping sunflower oil at low temperatures during manufacture and storage can help minimize rancidity and nutrient loss—as can storage in bottles that are made of either darkly-colored glass, or, plastic that has been treated with an ultraviolet light protectant.[citation needed]
[edit]
Sunflower oil can be extracted using chemical solvents (e.g., hexane), or expeller pressing (i.e., squeezed directly from sunflower seeds by crushing them).[14] «Cold-pressing» (or expeller pressing) sunflower seeds under low-temperature conditions is a method that does not use chemical solvents to derive sunflower seed oil.[citation needed]
Refined versus unrefined[edit]
Refining sunflower oil through solvent extraction, de-gumming, neutralization, and bleaching can make it more stable and suitable for high-temperature cooking, but doing so will also remove some of the oil’s nutrients, flavor, color (resulting in a pale-yellow), free fatty acids, phospholipids, polyphenols, and phytosterols. Also, some of the polyunsaturated fatty acids will be converted into trans fat due to the high temperatures involved in the process.[15][16] Unrefined sunflower oil is less heat-stable (and therefore well-suited to dishes that are raw, or cooked at low temperatures), but it will retain more of its original nutrient content, flavor, and color (light-amber).
Uses[edit]
In food preparation[edit]
Refined sunflower oil is used for low-to-extremely-high-temperature cooking. As a frying oil, it behaves as a typical vegetable triglyceride. Unrefined sunflower oil is a traditional salad dressing in Eastern European cuisines.[17] Sunflower oil is also an ingredient in sunflower butter.
Methods for cooking snack foods, such as potato chips or French fries, may use sunflower oil.[18][19]
Seed meal[edit]
Extraction of sunflower oil leaves behind the crushed seeds, typically referred to as seed meal, which is rich in protein and dietary fiber and used as an animal feed, fertilizer or fuel.[20]
Supplements[edit]
Sunflower oil dietary supplements have been marketed for treatment of eczema, but research has shown it is not medically effective.[21]
As fuel[edit]
Sunflower oil can be used to run diesel engines when mixed with diesel in the tank. Due to the high levels of unsaturated fats, there is higher viscosity in cold temperatures.[22]
Cosmetics industry[edit]
PEG-10 sunflower glycerides, a pale yellow liquid with a «slightly fatty» odor, are the polyethylene glycol derivative of the mono- and diglycerides derived from sunflower seed oil with an average of 10 moles of ethylene oxide.[23] PEG-10 sunflower glycerides are commonly used in cosmetic formulations.
Horticulture[edit]
In the European Union, and United Kingdom (since Brexit), sunflower oil is sprayed onto tomato crops as a fungicide to control powdery mildew from Oidium neolycopersici.[24] For this use it is classified as a ‘Basic Substance’ that can be used on both organic and conventional farms.[25]
Properties[edit]
The nutritional values are expressed as percent (%) by mass of total fat. | |||||||||
Type | Processing treatment[28] |
Saturated fatty acids |
Monounsaturated fatty acids |
Polyunsaturated fatty acids |
Smoke point | ||||
---|---|---|---|---|---|---|---|---|---|
Total[26] | Oleic acid (ω-9) |
Total[26] | α-Linolenic acid (ω-3) |
Linoleic acid (ω-6) |
ω-6:3 ratio |
||||
Avocado[29] | 11.6 | 70.6 | 52–66[30] | 13.5 | 1 | 12.5 | 12.5:1 | 250 °C (482 °F)[31] | |
Brazil nut[32] | 24.8 | 32.7 | 31.3 | 42.0 | 0.1 | 41.9 | 419:1 | 208 °C (406 °F)[33] | |
Canola[34] | 7.4 | 63.3 | 61.8 | 28.1 | 9.1 | 18.6 | 2:1 | 238 °C (460 °F)[33] | |
Coconut[35] | 82.5 | 6.3 | 6 | 1.7 | 175 °C (347 °F)[33] | ||||
Corn[36] | 12.9 | 27.6 | 27.3 | 54.7 | 1 | 58 | 58:1 | 232 °C (450 °F)[37] | |
Cottonseed[38] | 25.9 | 17.8 | 19 | 51.9 | 1 | 54 | 54:1 | 216 °C (420 °F)[37] | |
Cottonseed[39] | hydrogenated | 93.6 | 1.5 | 0.6 | 0.2 | 0.3 | 1.5:1 | ||
Flaxseed/linseed[40] | 9.0 | 18.4 | 18 | 67.8 | 53 | 13 | 0.2:1 | 107 °C (225 °F) | |
Grape seed | 10.5 | 14.3 | 14.3 | 74.7 | – | 74.7 | very high | 216 °C (421 °F)[41] | |
Hemp seed[42] | 7.0 | 9.0 | 9.0 | 82.0 | 22.0 | 54.0 | 2.5:1 | 166 °C (330 °F)[43] | |
Olive[44] | 13.8 | 73.0 | 71.3 | 10.5 | 0.7 | 9.8 | 14:1 | 193 °C (380 °F)[33] | |
Palm[45] | 49.3 | 37.0 | 40 | 9.3 | 0.2 | 9.1 | 45.5:1 | 235 °C (455 °F) | |
Palm[46] | hydrogenated | 88.2 | 5.7 | 0 | |||||
Peanut[47] | 16.2 | 57.1 | 55.4 | 19.9 | 0.318 | 19.6 | 61.6:1 | 232 °C (450 °F)[37] | |
Rice bran oil | 25 | 38.4 | 38.4 | 36.6 | 2.2 | 34.4[48] | 15.6 | 232 °C (450 °F)[49] | |
High-oleic safflower oil[50] | 7.5 | 75.2 | 75.2 | 12.8 | 0 | 12.8 | very high | 212 °C (414 °F)[33] | |
Sesame[51] | 14.2 | 39.7 | 39.3 | 41.7 | 0.3 | 41.3 | 138:1 | ||
Soybean[52] | 15.6 | 22.8 | 22.6 | 57.7 | 7 | 51 | 7.3:1 | 238 °C (460 °F)[37] | |
Soybean[53] | partially hydrogenated | 14.9 | 43.0 | 42.5 | 37.6 | 2.6 | 34.9 | 13.4:1 | |
Walnut oil[54] | unrefined | 9.1 | 22.8 | 22.2 | 63.3 | 10.4 | 52.9 | 5:1 | 160 °C (320 °F)[55] |
Sunflower[56] | 8.99 | 63.4 | 62.9 | 20.7 | 0.16 | 20.5 | 128:1 | 227 °C (440 °F)[37] |
References[edit]
- ^ a b «Four types of sunflower oil». National Sunflower Association. 2018. Retrieved 19 November 2018.
- ^ a b c d «Sunflower oil fatty acid profile» (PDF). National Sunflower Association. 2018. Retrieved 19 November 2018.
- ^ a b Badouin, H; Gouzy, J; Grassa, C. J; Murat, F; Staton, S. E; Cottret, L; Lelandais-Brière, C; Owens, G. L; Carrère, S; Mayjonade, B; Legrand, L; Gill, N; Kane, N. C; Bowers, J. E; Hubner, S; Bellec, A; Bérard, A; Bergès, H; Blanchet, N; Boniface, M. C; Brunel, D; Catrice, O; Chaidir, N; Claudel, C; Donnadieu, C; Faraut, T; Fievet, G; Helmstetter, N; King, M; et al. (2017). «The sunflower genome provides insights into oil metabolism, flowering and Asterid evolution». Nature. 546 (7656): 148–152. Bibcode:2017Natur.546..148B. doi:10.1038/nature22380. PMID 28538728.
- ^ Rauf S, Jamil N, Tariq SA, Khan M, Kausar M, Kaya Y (2017). «Progress in modification of sunflower oil to expand its industrial value». J Sci Food Agric. 97 (7): 1997–2006. doi:10.1002/jsfa.8214. PMID 28093767.
- ^ Christov M (2012). «Contribution of interspecific hybridization to sunflower breeding» (PDF). Helia. 35 (57): 37–46. doi:10.2298/hel1257037c. S2CID 85351878.
- ^ Alfred Thomas (2002). «Fats and Fatty Oils». Ullmann’s Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_173. ISBN 3527306730.
- ^ British Pharmacopoeia Commission (2005). «Ph Eur monograph 1371». British Pharmacopoeia 2005. Norwich, England: The Stationery Office. ISBN 0-11-322682-9.
- ^ a b «Sunflower oil production, 2019; Crops/Regions/World list/Production Quantity; unofficial data (pick lists)». UN Food and Agriculture Organization, Corporate Statistical Database (FAOSTAT). 2020. Retrieved 14 May 2022.
- ^ Alicia Ayerdi Gotor; Larbi Rhazi (2016). «Effects of refining process on sunflower oil minor components: a review». Oilseeds and Fats, Crops and Lipids. 23 (2): D207. doi:10.1051/ocl/2016007.
- ^ Skorić D, Jocić S, Sakac Z, Lecić N (2008). «Genetic possibilities for altering sunflower oil quality to obtain novel oils». Can J Physiol Pharmacol. 86 (4): 215–21. doi:10.1139/Y08-008. PMID 18418432.
{{cite journal}}
: CS1 maint: uses authors parameter (link) - ^ a b Chu, Michael (2004-06-10). «Smoke Points of Various Fats — Kitchen Notes». Cooking For Engineers. Retrieved 2013-02-07.
- ^ a b Irina NITA, Anisoara NEAGU, Sibel GEACAI, Anca DUMITRU and Anca STERPU: «Study of the behavior of some vegetable oils during the thermal treatment,» Technology and Chemical Engineering Department, Ovidius University, bd. Mamaia 124, Constanta, 900527, Romania http://www.univ-ovidius.ro/anale-chimie/chemistry/2010-1/full/1_nita.pdf Archived 2011-06-28 at the Wayback Machine
- ^ Esteban B, Riba J-R, Baquero G, Rius A, Puig R (2012). «Temperature dependence of density and viscosity of vegetable oils» (PDF). Biomass and Bioenergy. 42: 164–71. doi:10.1016/j.biombioe.2012.03.007. hdl:2117/16423.
{{cite journal}}
: CS1 maint: uses authors parameter (link) - ^ Cox, Jeff (April 1979). «The Sunflower Seed Huller and Oil Press». Organic Gardening. Rodale Press. Retrieved 26 June 2013.
- ^ Kemény, Z.; Recseg, K.; Hénon, G.; Kővári, K.; Zwobada, F. (2001). «Deodorization of vegetable oils: Prediction of trans polyunsaturated fatty acid content». Journal of the American Oil Chemists’ Society. 78 (9): 973–979. doi:10.1007/s11746-001-0374-0. S2CID 67792000.
- ^ Liu, W.; Lu, G. H. (2018). «Cis-trans isomerization of unsaturated fatty acids in edible oils to prepare trans fat». Grasas y Aceites. 69 (3): 268. doi:10.3989/gya.0225181. S2CID 105827306 – via ResearchGate.
- ^ Peter Vatrooshkin (2012). Easier Than a Steamed Turnip: Simple and Delicious Meatless Russian Recipes. Plutagora LLC. pp. 21–22, 26–28, 30. ISBN 9781938407017.
- ^ «How we make Lays Classic potato chips». Frito-Lay North America, Inc. 2017. Retrieved 16 February 2017.
- ^ «The best chips you have ever tasted». BBC Food Recipes. 2017. Retrieved 16 February 2017.
- ^ Lomascolo, A; Uzan-Boukhris, E; Sigoillot, J. C.; Fine, F (2012). «Rapeseed and sunflower meal: A review on biotechnology status and challenges». Applied Microbiology and Biotechnology. 95 (5): 1105–14. doi:10.1007/s00253-012-4250-6. PMID 22752367. S2CID 11723992.
- ^ Bath-Hextall FJ, Jenkinson C, Humphreys R, Williams HC (2012). «Dietary supplements for established atopic eczema». Cochrane Database Syst Rev (Systematic review). 2 (2): CD005205. doi:10.1002/14651858.CD005205.pub3. PMID 22336810.
- ^ Johnson, JJ. Meyer, RF. Krall, JM. Shroyer, JP. Schlegel, AJ. Falk, JS and Lee, CD. 2005. Agronomic Practices. In High Plains Sunflower Production Handbook. Kansas State University, Manhattan, KS [accessed 2014 October 22].
- ^ «Material Safety Data Sheet for Florasolvs PEG-10 Sunflower» (PDF).
- ^ Sharp, Dr Russell (2021-11-22). «Basic Substances; what are they and how can they used for pest and disease control on farms?». Eutrema. Retrieved 2021-12-06.
- ^ European Commission. «Finalised in the Standing Committee on Plants, Animals, Food and Feed at its meeting on 7 October 2016 in view of the approval of sunflower oil as basic substance in accordance with Regulation (EC) No 1107/2009 Sunflowerseed oil (sunflower oil) is derived from sunflower seeds (seeds of Helianthus annuus L.)» (PDF).
{{cite web}}
: CS1 maint: url-status (link) - ^ a b c «US National Nutrient Database, Release 28». United States Department of Agriculture. May 2016. All values in this table are from this database unless otherwise cited or when italicized as the simple arithmetic sum of other component columns.
- ^ «Fats and fatty acids contents per 100 g (click for «more details»). Example: Avocado oil (user can search for other oils)». Nutritiondata.com, Conde Nast for the USDA National Nutrient Database, Standard Release 21. 2014. Retrieved 7 September 2017. Values from Nutritiondata.com (SR 21) may need to be reconciled with most recent release from the USDA SR 28 as of Sept 2017.
- ^ «USDA Specifications for Vegetable Oil Margarine Effective August 28, 1996» (PDF).
- ^ «Avocado oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ Feramuz Ozdemir; Ayhan Topuz (May 2003). «Changes in dry matter, oil content and fatty acids composition of avocado during harvesting time and post-harvesting ripening period» (PDF). Elsevier. Retrieved 15 January 2020.
- ^ Marie Wong; Cecilia Requejo-Jackman; Allan Woolf (April 2010). «What is unrefined, extra virgin cold-pressed avocado oil?». Aocs.org. The American Oil Chemists’ Society. Retrieved 26 December 2019.
- ^ «Brazil nut oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ a b c d e Katragadda, H. R.; Fullana, A. S.; Sidhu, S.; Carbonell-Barrachina, Á. A. (2010). «Emissions of volatile aldehydes from heated cooking oils». Food Chemistry. 120: 59–65. doi:10.1016/j.foodchem.2009.09.070.
- ^ «Canola oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Coconut oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Corn oil, industrial and retail, all purpose salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ a b c d e Wolke, Robert L. (May 16, 2007). «Where There’s Smoke, There’s a Fryer». The Washington Post. Retrieved March 5, 2011.
- ^ «Cottonseed oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Cottonseed oil, industrial, fully hydrogenated, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Linseed/Flaxseed oil, cold pressed, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ Garavaglia J, Markoski MM, Oliveira A, Marcadenti A (2016). «Grape Seed Oil Compounds: Biological and Chemical Actions for Health». Nutrition and Metabolic Insights. 9: 59–64. doi:10.4137/NMI.S32910. PMC 4988453. PMID 27559299.
- ^ Callaway J, Schwab U, Harvima I, Halonen P, Mykkänen O, Hyvönen P, Järvinen T (April 2005). «Efficacy of dietary hempseed oil in patients with atopic dermatitis». The Journal of Dermatological Treatment. 16 (2): 87–94. doi:10.1080/09546630510035832. PMID 16019622. S2CID 18445488.
- ^ Melina, Vesanto. «Smoke points of oils» (PDF). veghealth.com. The Vegetarian Health Institute.
- ^ «Olive oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Palm oil, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Palm oil, industrial, fully hydrogenated, filling fat, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Oil, peanut». FoodData Central. usda.gov.
- ^ Orthoefer, F. T. (2005). «Chapter 10: Rice Bran Oil». In Shahidi, F. (ed.). Bailey’s Industrial Oil and Fat Products. Vol. 2 (6 ed.). John Wiley & Sons, Inc. p. 465. doi:10.1002/047167849X. ISBN 978-0-471-38552-3.
- ^ «Rice bran oil». RITO Partnership. Retrieved 22 January 2021.
- ^ «Safflower oil, salad or cooking, high oleic, primary commerce, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Oil, sesame, salad or cooking». FoodData Central. fdc.nal.usda.gov. 1 April 2019.
- ^ «Soybean oil, salad or cooking, fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Soybean oil, salad or cooking, (partially hydrogenated), fat composition, 100 g». US National Nutrient Database, Release 28, United States Department of Agriculture. May 2016. Retrieved 6 September 2017.
- ^ «Walnut oil, fat composition, 100 g». US National Nutrient Database, United States Department of Agriculture.
- ^ «Smoke Point of Oils». Baseline of Health. Jonbarron.org.
- ^ «FoodData Central». fdc.nal.usda.gov.
Unrefined sunflower oil with sunflower inflorescence
Refined high-oleic sunflower oil
Sunflower oil is the non-volatile oil pressed from the seeds of the sunflower (Helianthus annuus). Sunflower oil is commonly used in food as a frying oil, and in cosmetic formulations as an emollient.
Sunflower oil is primarily composed of linoleic acid, a polyunsaturated fat, and oleic acid, a monounsaturated fat. Through selective breeding and manufacturing processes, oils of differing proportions of the fatty acids are produced.[1] The expressed oil has a neutral taste profile.[2] The oil contains a large amount of vitamin E.[2]
As of 2017, genome analysis[3] and development of hybrid sunflowers to increase oil production are under development to meet greater consumer demand for sunflower oil and its commercial varieties.[4][5]
In 2018, Ukraine and Russia together accounted for 53% of the world’s production of sunflower oil.
Composition[edit]
Sunflower oil is mainly a triglyceride.[6] The British Pharmacopoeia lists the following profile:[7]
- Palmitic acid (saturated): 5%
- Stearic acid (saturated): 6%
- Oleic acid (monounsaturated omega-9): 30%
- Linoleic acid (polyunsaturated omega-6): 59%
Four types of sunflower oils with differing concentrations of fatty acids are produced through plant breeding and industrial processing: high-linoleic, high-oleic, mid-oleic, and high-stearic combined with high-oleic.[1][2]
- High-linoleic, 69% linoleic acid
- High-oleic, 82% oleic acid
- Mid-oleic, 65% oleic acid
- High-stearic with high-oleic, 18% stearic acid and 72% oleic acid[2]
Sunflower oil production – 2019 | |
---|---|
Country | (millions of tonnes) |
5.84 | |
5.42 | |
1.41 | |
1.10 | |
0.69 | |
0.53 | |
0.53 | |
0.52 | |
0.49 | |
0.32 | |
World | 20.29 |
Source: FAOSTAT of the United Nations[8] |
In an analysis of the sunflower genome to reveal plant metabolism producing its oil, phytosterols were identified,[3] as confirmed in another analysis of sunflower oil components, including polyphenols, squalene, and terpenoids.[9]
Production[edit]
Sunflower oil in the Silpo store in Kyiv, Ukraine. August 2021.
In 2018, world production of sunflower oil was 18 million tonnes, led by Ukraine and Russia as the leading producers accounting together for 53% of the world total.[8]
In 2022, there is a global shortage of sunflower oil due to the 2022 Russian invasion of Ukraine which has led to over 50% drop in the availability of sunflower oil. Due to the shortages many brands are reforming their recipes by switching to rapeseed oil to allow the production of their products to continue.
Nutrition[edit]
Nutritional value per 100 g (3.5 oz) | |
---|---|
Energy | 3,699 kJ (884 kcal) |
Carbohydrates |
0 g |
Fat |
100 g |
Saturated | 9.748 g |
Monounsaturated | 83.594 g |
Polyunsaturated | 3.798 g |
Protein |
0 g |
Vitamins | Quantity
%DV† |
Vitamin E |
274% 41.08 mg |
Vitamin K |
5% 5.4 μg |
|
|
†Percentages are roughly approximated using US recommendations for adults. Source: USDA FoodData Central |
Nutritional value per 100 g (3.5 oz) | |
---|---|
Energy | 3,699 kJ (884 kcal) |
Carbohydrates |
0 g |
Fat |
100 g |
Saturated | 10.3 g |
Monounsaturated | 19.5 g |
Polyunsaturated | 65.7 g |
Protein |
0 g |
Vitamins | Quantity
%DV† |
Vitamin E |
274% 41.08 mg |
Vitamin K |
5% 5.4 μg |
|
|
†Percentages are roughly approximated using US recommendations for adults. Source: USDA FoodData Central |
Nutritional value per 100 g (3.5 oz) | |
---|---|
Energy | 3,699 kJ (884 kcal) |
Carbohydrates |
0 g |
Fat |
100 g |
Saturated | 9.009 g |
Monounsaturated | 57.344 g |
Polyunsaturated | 28.962 g |
Protein |
0 g |
Vitamins | Quantity
%DV† |
Vitamin E |
274% 41.08 mg |
Vitamin K |
5% 5.4 μg |
|
|
†Percentages are roughly approximated using US recommendations for adults. Source: USDA FoodData Central |
Several varieties of sunflower oil seeds have been developed by standard plant breeding methods, mainly to vary the amounts of oleic acid and linoleic acid which, respectively, are the predominant monounsaturated and polyunsaturated fats in sunflower oil.[10] Sunflower oil is a rich source of vitamin E (tables).
Physical properties[edit]
Sunflower oil is liquid at room temperature. The refined oil is clear and slightly amber-colored with a slightly fatty odour.
Smoke point (refined) | 232 °C | 450 °F[11] |
Smoke point (unrefined) | 107 °C | 225 °F[11] |
Density (25 °C) | 918.8 kg/m3[12] | |
Refractive index (25 °C) | ≈1.4735[12] | |
Saponification value | 188-194 | |
Iodine value | 120-145 | |
Unsaponifiable matter | 1.5-2.0% | |
Viscosity (25 °C), unrefined | 0.04914
kg/(m*s)[13] |
Preparation and storage[edit]
Because sunflower oil is primarily composed of less-stable polyunsaturated and monounsaturated fatty acids, it can be particularly susceptible to degradation by heat, air, and light, which trigger and accelerate oxidation. Keeping sunflower oil at low temperatures during manufacture and storage can help minimize rancidity and nutrient loss—as can storage in bottles that are made of either darkly-colored glass, or, plastic that has been treated with an ultraviolet light protectant.[citation needed]
[edit]
Sunflower oil can be extracted using chemical solvents (e.g., hexane), or expeller pressing (i.e., squeezed directly from sunflower seeds by crushing them).[14] «Cold-pressing» (or expeller pressing) sunflower seeds under low-temperature conditions is a method that does not use chemical solvents to derive sunflower seed oil.[citation needed]
Refined versus unrefined[edit]
Refining sunflower oil through solvent extraction, de-gumming, neutralization, and bleaching can make it more stable and suitable for high-temperature cooking, but doing so will also remove some of the oil’s nutrients, flavor, color (resulting in a pale-yellow), free fatty acids, phospholipids, polyphenols, and phytosterols. Also, some of the polyunsaturated fatty acids will be converted into trans fat due to the high temperatures involved in the process.[15][16] Unrefined sunflower oil is less heat-stable (and therefore well-suited to dishes that are raw, or cooked at low temperatures), but it will retain more of its original nutrient content, flavor, and color (light-amber).
Uses[edit]
In food preparation[edit]
Refined sunflower oil is used for low-to-extremely-high-temperature cooking. As a frying oil, it behaves as a typical vegetable triglyceride. Unrefined sunflower oil is a traditional salad dressing in Eastern European cuisines.[17] Sunflower oil is also an ingredient in sunflower butter.
Methods for cooking snack foods, such as potato chips or French fries, may use sunflower oil.[18][19]
Seed meal[edit]
Extraction of sunflower oil leaves behind the crushed seeds, typically referred to as seed meal, which is rich in protein and dietary fiber and used as an animal feed, fertilizer or fuel.[20]
Supplements[edit]
Sunflower oil dietary supplements have been marketed for treatment of eczema, but research has shown it is not medically effective.[21]
As fuel[edit]
Sunflower oil can be used to run diesel engines when mixed with diesel in the tank. Due to the high levels of unsaturated fats, there is higher viscosity in cold temperatures.[22]
Cosmetics industry[edit]
PEG-10 sunflower glycerides, a pale yellow liquid with a «slightly fatty» odor, are the polyethylene glycol derivative of the mono- and diglycerides derived from sunflower seed oil with an average of 10 moles of ethylene oxide.[23] PEG-10 sunflower glycerides are commonly used in cosmetic formulations.
Horticulture[edit]
In the European Union, and United Kingdom (since Brexit), sunflower oil is sprayed onto tomato crops as a fungicide to control powdery mildew from Oidium neolycopersici.[24] For this use it is classified as a ‘Basic Substance’ that can be used on both organic and conventional farms.[25]
Properties[edit]
The nutritional values are expressed as percent (%) by mass of total fat. | |||||||||
Type | Processing treatment[28] |
Saturated fatty acids |
Monounsaturated fatty acids |
Polyunsaturated fatty acids |
Smoke point | ||||
---|---|---|---|---|---|---|---|---|---|
Total[26] | Oleic acid (ω-9) |
Total[26] | α-Linolenic acid (ω-3) |
Linoleic acid (ω-6) |
ω-6:3 ratio |
||||
Avocado[29] | 11.6 | 70.6 | 52–66[30] | 13.5 | 1 | 12.5 | 12.5:1 | 250 °C (482 °F)[31] | |
Brazil nut[32] | 24.8 | 32.7 | 31.3 | 42.0 | 0.1 | 41.9 | 419:1 | 208 °C (406 °F)[33] | |
Canola[34] | 7.4 | 63.3 | 61.8 | 28.1 | 9.1 | 18.6 | 2:1 | 238 °C (460 °F)[33] | |
Coconut[35] | 82.5 | 6.3 | 6 | 1.7 | 175 °C (347 °F)[33] | ||||
Corn[36] | 12.9 | 27.6 | 27.3 | 54.7 | 1 | 58 | 58:1 | 232 °C (450 °F)[37] | |
Cottonseed[38] | 25.9 | 17.8 | 19 | 51.9 | 1 | 54 | 54:1 | 216 °C (420 °F)[37] | |
Cottonseed[39] | hydrogenated | 93.6 | 1.5 | 0.6 | 0.2 | 0.3 | 1.5:1 | ||
Flaxseed/linseed[40] | 9.0 | 18.4 | 18 | 67.8 | 53 | 13 | 0.2:1 | 107 °C (225 °F) | |
Grape seed | 10.5 | 14.3 | 14.3 | 74.7 | – | 74.7 | very high | 216 °C (421 °F)[41] | |
Hemp seed[42] | 7.0 | 9.0 | 9.0 | 82.0 | 22.0 | 54.0 | 2.5:1 | 166 °C (330 °F)[43] | |
Olive[44] | 13.8 | 73.0 | 71.3 | 10.5 | 0.7 | 9.8 | 14:1 | 193 °C (380 °F)[33] | |
Palm[45] | 49.3 | 37.0 | 40 | 9.3 | 0.2 | 9.1 | 45.5:1 | 235 °C (455 °F) | |
Palm[46] | hydrogenated | 88.2 | 5.7 | 0 | |||||
Peanut[47] | 16.2 | 57.1 | 55.4 | 19.9 | 0.318 | 19.6 | 61.6:1 | 232 °C (450 °F)[37] | |
Rice bran oil | 25 | 38.4 | 38.4 | 36.6 | 2.2 | 34.4[48] | 15.6 | 232 °C (450 °F)[49] | |
High-oleic safflower oil[50] | 7.5 | 75.2 | 75.2 | 12.8 | 0 | 12.8 | very high | 212 °C (414 °F)[33] | |
Sesame[51] | 14.2 | 39.7 | 39.3 | 41.7 | 0.3 | 41.3 | 138:1 | ||
Soybean[52] | 15.6 | 22.8 | 22.6 | 57.7 | 7 | 51 | 7.3:1 | 238 °C (460 °F)[37] | |
Soybean[53] | partially hydrogenated | 14.9 | 43.0 | 42.5 | 37.6 | 2.6 | 34.9 | 13.4:1 | |
Walnut oil[54] | unrefined | 9.1 | 22.8 | 22.2 | 63.3 | 10.4 | 52.9 | 5:1 | 160 °C (320 °F)[55] |
Sunflower[56] | 8.99 | 63.4 | 62.9 | 20.7 | 0.16 | 20.5 | 128:1 | 227 °C (440 °F)[37] |
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