Vegetable oils, or vegetable fats, are oils extracted from seeds, or less often, from other parts of fruits. Like animal fats, vegetable fats are mixtures of triglycerides. Soybean oil, rapeseed oil, and cocoa butter are examples of fats from seeds.
Tech Startup Growth Hacking 101 - Basics on Growth Marketing
Â
Vegetable oil
1. Vegetable oil
Â
Vegetable oils, or vegetable fats, are oils extracted from seeds, orÂ
less often, from other parts of fruits. Like animal fats, vegetableÂ
fats are mixtures of triglycerides. Soybean oil, rapeseed oil, andÂ
cocoa butter are examples of fats from seeds. Olive oil, palm oil, andÂ
rice bran oil are examples of fats from other parts of fruits. InÂ
common usage, vegetable oil may refer exclusively to vegetable fatsÂ
which are liquid at room temperature. Vegetable oils are usuallyÂ
edible; non-edible oils derived mainly from petroleum are termedÂ
mineral oils.Â
2. Uses of triglyceride vegetable oilÂ
Uses in antiquity Â
Oils extracted from plants have been used since ancient times andÂ
in many cultures. As an example, in a 4,000-year-old kitchenÂ
unearthed in Indiana's Charlestown State Park, archaeologist BobÂ
McCullough of Indiana University-Purdue University Fort WayneÂ
found evidence that large slabs of rock were used to crush hickoryÂ
nuts and the oil was then extracted with boiling water. Â
AddressBazar.com is an Bangladeshi Online Yellow Page. From here you
will find important and necessary information of various ​Vegetable Oil
Companies in Bangladesh.
Archaeological evidence shows that olives were turned into olive oilÂ
by 6000 BCE and 4500 BCE in present-day Israel and Palestine.Â
In addition to food, fats and oils (both vegetable and mineral) haveÂ
long been used as fuel, typically in lamps which were a principalÂ
source of illumination in ancient times. Oils may have been used forÂ
lubrication, but there is no evidence for this. Vegetable oils wereÂ
probably more valuable as food and lamp-oil; Babylonian mineralÂ
oil was known to be used as fuel, but there are no references toÂ
lubrication. Pliny the Elder reported that fats such as lard were usedÂ
to lubricate the axles of carts.Â
Â
3. Â
Â
Â
Culinary uses Â
Â
Many vegetable oils are consumed directly, or indirectly asÂ
ingredients in food – a role that they share with some animal fats,Â
including butter, ghee, ​lard​, and schmaltz. The oils serve a numberÂ
of purposes in this role:Â
â—Ź Shortening – to give the pastry a crumbly texture.Â
â—Ź Texture – oils can serve to make other ingredients stickÂ
together less.Â
4. â—Ź Flavor – while less flavorful oils command premium prices,Â
some oils, such as olive, sesame, or almond oil, may beÂ
chosen specifically for the flavor they impart.Â
â—Ź Flavor base – oils can also "carry" flavors of otherÂ
ingredients, since many flavors are due to chemicals thatÂ
are soluble in oil.Â
Oils can be heated to temperatures significantly higher than theÂ
boiling point of water, 100 °C (212 °F), and used to cook foodsÂ
(frying). Oils for this purpose must have a high flash point. SuchÂ
oils include the major ​cooking ​oils – ​soybean​, ​rapeseed​, ​canola​,Â
sunflower, safflower, peanut, cottonseed, etc. Tropical oils, such asÂ
coconut​, pa​lm​, and ​rice ​bran oils, are particularly valued in AsianÂ
cultures for high-temperature cooking, because of their unusuallyÂ
high flash points.Â
Hydrogenated oilsÂ
Unsaturated vegetable oils can be transformed through partial orÂ
complete "hydrogenation" into oils of higher melting point. TheÂ
hydrogenation process involves "sparging" the oil at highÂ
temperature and pressure with hydrogen in the presence of aÂ
catalyst, typically a powdered nickel compound. As eachÂ
carbon-carbon double-bond is chemically reduced to a single bond,Â
two hydrogen atoms each form single bonds with the two carbonÂ
atoms. The elimination of double bonds by adding hydrogen atomsÂ
is called saturation; as the degree of saturation increases, the oilÂ
5. progresses ​toward ​being fully hydrogenated. An oil may beÂ
hydrogenated to increase resistance to rancidity (oxidation) or toÂ
change its physical characteristics. As the degree of saturationÂ
increases, the oil's viscosity and melting point increase.Â
The use of hydrogenated oils in foods has never been completelyÂ
satisfactory. Because the center arm of the triglyceride is shieldedÂ
somewhat by the end fatty acids, most of the hydrogenation occursÂ
on the end fatty acids, thus making the resulting fat more brittle. AÂ
margarine made from naturally more saturated oils will be moreÂ
plastic (more "spreadable") than a margarine made fromÂ
hydrogenated soy oil. While full hydrogenation produces largelyÂ
saturated fatty acids, partial hydrogenation results in theÂ
transformation of unsaturated cis fatty acids to unsaturated transÂ
fatty acids in the oil mixture due to the heat used in hydrogenation.Â
Partially hydrogenated oils and their trans fats have been linked toÂ
an increased risk of mortality from coronary heart disease, amongÂ
other increased health risks.Â
In the US, the Standard of Identity for a product labeled asÂ
"vegetable oil margarine" specifies only canola, safflower,Â
sunflower, corn, soybean, or peanut oil may be used. Products notÂ
labeled "vegetable oil margarine" do not have that restriction.Â
Â
Â
6. Industrial uses Â
Vegetable oils are used as an ingredient or component in manyÂ
manufactured products.Â
Many ​vegetable ​oils are used to make soaps, skin products, candles,Â
perfumes and other personal care and cosmetic products. Some oilsÂ
are particularly suitable as drying oils, and are used in makingÂ
paints and other wood treatment products. Dammar oil (a mixtureÂ
of linseed oil and dammar resin), for example, is used almostÂ
exclusively in treating the hulls of wooden boats. Vegetable oils areÂ
increasingly being used in the electrical industry as insu​lators​ asÂ
vegetable oils are not toxic to the environment, biodegradable ifÂ
spilled and have high flash and fire points. However, vegetable oilsÂ
are less stable chemically, so they are generally used in systemsÂ
where they are not exposed to oxygen, and they are more expensiveÂ
than crude oil distillate. Synthetic tetraesters, which are similar toÂ
vegetable oils but with four fatty acid chains compared to theÂ
normal three found in a natural ester, are manufactured by FischerÂ
esterification. Tetraesters generally have high stability to oxidationÂ
and have found use as engine lubricants. Vegetable oil is being usedÂ
to produce biodegradable hydraulic fluid and lubricant.Â
One limiting factor in industrial uses of vegetable oils is that allÂ
such oils are susceptible to becoming rancid. Oils that are moreÂ
stable, such as ben oil or mineral oil, are thus preferred forÂ
7. industrial uses. ​Castor oil​ has numerous industrial uses, owing toÂ
the presence of hydroxyl groups on the fatty acid. Castor oil is aÂ
precursor to Nylon 11.Â
Pet food additive Â
Vegetable oil is used in the production of some pet foods. AAFCOÂ
defines​ v​e​getable o​il, in this context, as the product of vegetableÂ
origin obtained by extracting the oil from seeds or fruits which areÂ
processed for edible purposes.Â
FuelÂ
Â
Main article: Vegetable oil fuelÂ
8. Vegetable oils are also used to make biodiesel, which can be usedÂ
like conventional diesel. Some vegetable oil blends are used inÂ
unmodified vehicles but straight vegetable oil, also known as pureÂ
plant oil, needs specially prepared vehicles which have a method ofÂ
heating the oil to reduce its viscosity. The use of vegetable oils asÂ
alternative energy is growing and the availability of biodieselÂ
around the world is increasing.Â
The NNFCC estimates that the total net greenhouse gas savingsÂ
when using vegetable oils in place of fossil fuel-based alternativesÂ
for fuel production, range from 18 to 100%.Â
Production Â
The production process of ​vegetable oil​ involves the removal of oilÂ
from plant components, typically seeds. This can be done viaÂ
mechanical extraction using an oil mill or chemical extractionÂ
using a solvent. The extracted oil can then be purified and, ifÂ
required, refined or chemically altered.Â
Mechanical extraction Â
Oils can be removed via mechanical extraction, termed "crushing"Â
or "pressing." This method is typically used to produce the moreÂ
traditional oils (e.g., olive, coconut etc.), and it is preferred by mostÂ
"health-food" customers in the United States and in Europe. ThereÂ
are several different types of mechanical extraction.Â
9. Expeller-pressing extraction is common, though the screw press,Â
ram press, and ghani (powered mortar and pestle) are also used.Â
Oilseed presses are commonly used in developing countries, amongÂ
people for whom other extraction methods would be prohibitivelyÂ
expensive; the ghani is primarily used in India. The amount of oilÂ
extracted using these methods varies widely, as shown in theÂ
following table for extracting mowrah butter in India:Â
Solvent extraction Â
The processing of vegetable oil in commercial applications isÂ
commonly done by chemical extraction, using solvent extracts,Â
which produces higher yields and is quicker and less expensive. TheÂ
most common solvent is petroleum-derived hexane. This techniqueÂ
is used for most of the "newer" industrial oils such as soybean andÂ
corn oils. After extraction, the solvent is evaporated out by heatingÂ
the mixture to about 300 °F (149 °C).Â
Supercritical carbon dioxide​ can be used as a non-toxic alternativeÂ
to other solvents.Â
Hydrogenation Â
Oils may be partially hydrogenated to produce various ingredientÂ
oils. Lightly hydrogenated oils have very similar physicalÂ
characteristics to regular soy oil, but are more resistant toÂ
becoming rancid. Margarine oils need to be mostly solid at 32 °C (90Â
10. °F) so that the margarine does not melt in warm rooms, yet it needsÂ
to be completely liquid at 37 °C (98 °F), so that it doesn't leave aÂ
"lardy" taste in the mouth.Â
Hardening vegetable oil is done by raising a blend of vegetable oilÂ
and a catalyst in a near-vacuum to very high temperatures, andÂ
introducing hydrogen. This causes the carbon atoms of the oil toÂ
break double-bonds with other carbons, each carbon forming a newÂ
single-bond with a hydrogen atom. Adding these hydrogen atomsÂ
to the oil makes it more solid, raises the smoke point, and makesÂ
the oil more stable.Â
Â
11. Hydrogenated vegetable oils differ in two major ways from otherÂ
oils which are equally saturated. During hydrogenation, it is easierÂ
for hydrogen to come into contact with the fatty acids on the end ofÂ
the triglyceride, and less easy for them to come into contact withÂ
the center fatty acid. This makes the resulting fat more brittle thanÂ
a tropical oil; soy margarines are less "spreadable". The otherÂ
difference is that trans fatty acids (often called trans Â
fat) are formed in the hydrogenation reactor, and may amount to asÂ
much as 40 percent by weight of a partially hydrogenated oil.Â
Hydrogenated oils, especially partially hydrogenated oils with theirÂ
higher amounts of trans fatty acids, are increasingly thought to beÂ
unhealthy.Â
Deodorization
In the processing of edible ​oils​, the oil is heated under vacuum toÂ
near the smoke point or to about 450 °F (232 °C), and water isÂ
introduced at the bottom of the oil. The water immediately isÂ
converted to steam, which bubbles through the oil, carrying with itÂ
any chemicals which are water-soluble. The steam spargingÂ
removes impurities that can impart unwanted flavors and odors toÂ
the oil. Deodorization is key to the manufacture of vegetable oils.Â
Nearly all soybean, corn, and canola oils found on supermarketÂ
shelves go through a deodorization stage that removes traceÂ
amounts of odors and flavors, and lightens the color of the oil.Â
12. Occupational exposure Â
People can breathe in vegetable oil mist in the workplace. The U.S.Â
Occupational Safety and Health Administration (OSHA) has set theÂ
legal limit (permissible exposure limit) for vegetable oil mistÂ
exposure in the workplace as 15 mg/m​3​
total exposure and 5 mg/m​3
Â
respiratory exposure over an 8-hour workday. The U.S. NationalÂ
Institute for Occupational Safety and Health (NIOSH) has set aÂ
recommended exposure limit (REL) of 10 mg/m​3​
total exposure andÂ
5 mg/m​3​
respiratory exposure over an 8-hour workday.Â
Â