CHAPTER ONE
1.0INTRODUCTION
1.1 EDIBLE OIL
Edible oils are essential ingredients for our daily diet that serve as a transporter
for vitamins that are fat soluble, provide energy, and those essential to human
health. Edible oils are also known as cooking oils, which are mostly extracted
from plants and animals. According to the Canadian government, the definition
of an edible oil is "a substance of food, which should not be from any dairy
product and, whatever its composition, source, or whatever its origin, that is
completely synthesized for consumption of humans or in part from a fat or oil
other than that of milk. Regarding nutritional requirements, many modifications
of ingesting dietary fats have been seen over the years, although worldwide
health organizations have continuously been emphasizing dietary guidelines to
reduce the utilization levels of saturated and trans-fats. These fats have negative
effects on cardiovascular health, which is associated with enhancing the levels
of low-density lipoprotein (LDL), also known as "bad cholesterol". Contrary to
that, both unsaturated fats (mono and poly) tend to reduce LDL levels. Owing to
that, nutritional guidelines endorse replacing saturated and trans-fats with
unsaturated fats in our diet. Recently, it has been declared that saturated fats are
not that bad as they were perceived to be. Com- pared with that, trans-fats and
exchange of carbohydrates with saturated fats (to reduce intake of saturated
fats) is actually a bad option. The sunflower and soybean oils are decent sources
1
of polyunsaturated fats, whereas the canola and olive oils are best sources of
monounsaturated oils. To overcome hazards of cardiovascular diseases, use of
non- hydrogenated unsaturated oils such as sunflower and soybean is better
compared with palm oil. Several factors are responsible for the deterioration of
edible oil quality such as harvesting and packaging systems, agronomic
practices, ripening stage, seasonal conditions, and sanitary state of drupes,
processing technologies, and storage duration. To avoid likely adulterations and
to check the oil quality, several analytical techniques are used.
1.2 SOURCES OF EDIBLE OIL
There are a wide variety of cooking oils from plant sources such as olive oil,
palm oil, soybean oil, canola oil (rapeseed oil), corn oil, peanut oil and other
vegetable oils, as well as animal- based oils like butter and lard. Oil can be
flavored with aromatic foodstuffs such as herbs, chilies or garlic.
1.3 IMPORTANCE OF EDIBLE OIL
The demand for edible oils for cooking is increasing in developing countries of
Middle East, Africa, and Asia. In the United States, marketing of saturated fats
and popular public education about advantages of edible oils are used to
convince people to use edible oils. The edible oils also play an important role in
human nutrition and our daily life food. They are used as nutritional
components but not as particular essential fatty acids such as tocopherols,
2
phytosterols, phenolic compounds, and vitamins, which further- more
extraordinarily influence the flavor and taste of food. It has been proven that the
quality of fat, besides the quantity of fat, has a major effect on user's health. The
Public Health Institutes of many countries as well as international organizations,
Le. FAT/ OMS, have suggested through publications about daily absorption of
different types of fatty acids, such as SEA, monounsaturated fatty acids
(MUFA), and polyunsaturated fatty acids (PUFA). These commonly check the
SFA absorption, and stimulate the destruction of MUFA and PUFA. Nowadays,
oils rich in unsaturated fatty acids are pre- scribed as components of saturated
fats used in industrialized countries.
Oils and fats are used as major sources for energy. Lipids play a basic role as a
structural ingredient of cell walk. In food, lipids give flavor, physical
appearance, and mouth fresh products. Furthermore, fats and oils work as
heating media. Some of them come from direct interaction of lipids and their
degeneration products with food components. More than 95% of the world's
biodiesel is manufactured from edible oils, which is simply accessible from
agricultural industries. Biodiesels are also useful in recycling degradable lands.
In fact, biodiesel production in rural areas provides employment to people.
Biodiesel incorporates neutral chemicals in the air, which is why it is used to
neutralize the land's toxicity.
3
Nonedible plants have been considered as pressing agents for the manufacturing
of biodiesel. The utilization of nonedible oils along with edible oils has been
significant in the progress of many countries. The edible oils are mainly used as
food because they are too costly to be used as fuel. The nonedible oils are found
in nature on a large scale throughout the world. These essential oils are used to
preserve food by bioactive edible coatings. As we know, natural antimicrobials
in essential oils have been intensively studied. Essential oils (EO) are available
on a large scale for action. Hence, microorganisms and foodborne and
postharvest pathogens are sensitive to these antimicrobials. Although, due to the
huge embryonic of essential oils, their uses in the food manufacturing residue
are modified generally due to their intense aroma and toxicity problems. Many
authors have reported changes in the organoleptic properties of a food when
these oils are used. Edible coatings have currently achieved a landmark in the
field of food preservation due to promising results. Biodegradable films can
improve the variety of food products. Edible oils are the major source of fats
and vitamin E in our diet. These are also used for food cooking purposes. Edible
oils are also known as vegetable oils. These are also a source of omega 3 fatty
acids for the body, hence reducing the chances of breast cancer and heart
diseases. For cell growth and protection, vitamin E is an essential compound in
the body. Vitamin E-rich vegetable oils are obtained from almond, cottonseed,
sunflower, safflower, and wheat germ. It is also used to protect body tissues
such as breasts, eyes, skin, liver, and testes. Oleic acid and hydroxytyrosol
4
found in olive oil disturbs the occurrence of acute pancreatitis. Scientists have
discovered that the segments of extra virgin olive oil could be helpful in
protecting acute pancreatitis. Some of the edible oils, i.e., almond oil, peanut
oil, and wheat germ oils, have vitamin E, which benefits our body because it
plays an important role in the improvement of the immune system. These oils
work as enemies of oxidants and secure the distinctive body tissues, for
example, liver, skin, eyes, testes, and preventing heart illnesses. Vitamin E is an
antioxidant, which controls free radicals, and helps to prevent blood clusters and
blockages in coronary arteries, therefore helping prevent cardiovascular
illnesses.
1.4 OIL EXTRACTION METHOD
Two different methods for the extraction of oil from prepared seeds are used, ie,
chemical and mechanical oil extraction methods. The chemical extraction
method uses n-hexane solvents, whereas the other uses electric power in the oil
extraction process. Both processes are managed to determine the optimized
moisture contents for high oil yield.
1.4.1 MECHANICAL EXTRACTION
In the case of mechanical process, oil extraction is the most convenient method.
In this process, both manual ram press and an engine-driven screw press are
used. In this method, properly dried leaf seed is used for the oil extraction. By
5
using a screw press, it is difficult to process the seed. In an experiment, three
grated samples and whole seeds are used. Blender machine is used for the
grinding purpose. It has been observed that it takes several hours to process one
sample under the control of an operator. This is required to check the efficiency
of the machine. That is why the rate of reaction is slow. It has been shown that
the grinded seeds provide higher oil yield than the non-grinded seeds [20]. It is
declared that oil yield by ram press has 60%-65% efficiency, whereas 68%-80%
efficiency is achieved by the screw press. It is reported that mechanical press is
not suitable for extracting oil, owing to the issues related with nonedible oil
seeds. Moreover, with 15% absolute moisture contents, most compatible oil
yield is obtained. In addition to that, the extraction of oil from leaf involves the
changing of parameters by using screw press in the machine. These parameters
involve compression ratio, pressure, speed, and hot pressing.
1.4.2 SOLVENT OR CHEMICAL EXTRACTION
In this process, excessive components are removed by using liquid solvent from
solid. This process is also known as leaching. Chemical extraction done by
using n-hexane method gives high efficiency of oil yield. In this method, oil is
extracted using three grated samples of seeds. Dried samples of seed are grinded
in the coffee grinder and blended to maximize the particle size in the chemical
oil extraction method. The n-hexane with 2:1 ml. (hexane seed) ratio are added
in the grinded seed placed in a conical flask. Initially, the mixture is stirred to
6
dissolve all seeds in hexane. The opening of the conical flask is placed in an
incubator for 20 to 24h and is wrapped with aluminum foil. For solvent
evaporation, the mixture of hexane is now filtered into aluminum foil. For good
oil recovery, five-time extraction is completed. When it is confirmed that the
hexane is fully evaporated from the oil, then for further processing oil is
transferred into a container. Solvent extraction method is vastly more
successful, with approximately 54% for the oil yield. However, the cost of
solvent is the major barrier.
1.5 STATEMENT OF PROBLEM
To give value addition and for health benefits.
1.6 AIM:
To compare the soybean oil, groundnut oil and melon seed oil to know the oil
with more health benefit and which of them will add more value to industrialist
during the production.
1.7 SIGNIFICANCE OF STUDY:
My interest in groundnut and melon seed oil is that melon seed is been
cultivated in Nigeria and it's affordable. A groundnut has a lower shelf life that
if you did not extract oil, the whole groundnut will spoil, that extracting the oil
will add value to the groundnut.
7
CHAPTER 2
2.0 LITERATURE REVIEW
2.1 MELON SEED
Watermelon seed oil, rich in linoleic acid (~64.5%), is used for frying and
cooking in some African and Middle Eastern American countries owning to its
unique flavor (Akoh, C.C, and C.V. Nwosu, 2008). Much research has been
published on the oxidative stability of vegetable or fruit oils, but a little has
been reported on the stability of melon seed oil. The modification of melon seed
oil fatty acid composition by incorporation of oleic acid (18:1) has been
explored (Charment, O. Moussata, and C.C. Akoh, 2007). The modified melon
seed oil was produced with the better balance of monounsaturate (18:1) and
essential fatty acids (18:2), and also improved the seed oil oxidative stability
and nutritional value (Charment, O. Moussata, and C.C. Akoh, 2010). Thus, the
seed oil composition of the domestic watermelon was evaluated in the current
study, which had not been previously investigated. These data may help in the
selection of melon seed oil for future commercial production in human diet.
2.2 GROUNDNUT SEED
Groundnut (Arachis hypogaea L.) is a native to eastern region of South
America. It is grown as an annual crop purposely for its edible oil and protein
rich seeds. The groundnut is an herbaceous plant with many cultivars, common
8
in the United States, grow up to 30-46 cm high. Runner varieties, the most
common in the West African countries are shorter and run along the ground for
30-60 cm (Atasie et al., 2009). The peanut plant produces yellow, orange or
white flowers which produce 'pegs', characteristic floral structures which sink
into the ground to grow the pod. The pods can reach up to 10 cm in length and
can contain between 1 and 5 seeds, depending on the varieties (Krapovickan et
al., 2007). Vegetable oils are widely consumed domestically in Nigeria and
other parts of the world. It is used primarily as a cooking and salad oil. Studies
have shown that groundnut oil.
2.3 SEED PREPARATION METHODS
Oil extraction from seed involves the elimination of external layer of plants to
open up the seed of the plant and then drying the seed up to the desired moisture
content. At room temperature, the dried seeds are cleaned, sieved, and then
stored for 3-4 days. The seeds are also dried in an oven at 65°C to 700°C.
2.4 SEED EXTRACTION
In the first step, the outer layer of the seed is removed to expose the seed. For
further processing, the seeds are cracked open. This process involves two
methods: mallets and stompers. For the mallet, an operator cracks the seed
individually before removing the waste husk and seeds on the surface. For the
stomper, the process does not stop until the large numbers of seed are cracked;
9
those seeds are placed on the ground and then waste husk or seeds are removed.
By the stomper, numerous seeds are cracked at a time, whereas by the mallet,
seeds are cracked individually. It is also observed that, rather than steel or
wooden-headed mallets, rubber-headed mallets are preferred because they
rebound excessively. The efficiency of the stomper is reduced due to variability
in size of seed. In fact, the largest seeds are stuck in each blow. Extraction of
seeds is a labor-intensive and time-consuming process. However, it has been
estimated that 2 to 3kg of seeds per hour are cracked. Both methods have equal
efficiency of seed-cracking rate.
2.5 SEED DRYING
To obtain high oil yield, the seed must contain optimum moisture contents. It is
observed that, in the solvent and mechanical extraction methods, the highest oil
yield from seeds is with 15% seed moisture contents. This is when the seeds are
dried before oil extraction under temperature control using laboratory-scale
Clayson electric oven. The dried samples of seeds are placed in aluminum foil
trays and stored in a refrigerator.
2.6.1 SATURATED FATS CONTENT IN MELON OIL
Eleven fatty acids were identified in the Cucumis melo lipid fraction.
Concerning the saturated fatty acids, most of them were palmitic (14.4%) and
stearic (5.81%). For the unsaturated fatty acids, linoleic (59.2%) and oleic
10
(23.5%) stand. Saturated fatty acids in melon seed oil were undecanoic (C11),
myristic (C14), palmitic (C16) and stearic (C18). Palmitic and stearic acid were
(12, 13, and 13 mg/100 g), (13, 13, and 15 mg/100 g) for EO1, E02 and EO3,
respectively.
2.6.2 SATURATED FATS CONTENT IN GROUNDNUT OIL
It is a vegetable oil that is naturally trans-fat-free, cholesterol free, and low in
saturated fats. Peanut oil is high in unsaturated fats, especially monounsaturated
fat, which is also found in olive oil. It is also a source of the antioxidant vitamin
E and phytosterols, which benefit heart health
2.7 HEALTH BENEFITS OF EDIBLE OIL
The properties of these vegetable oils include their high content of unsaturated
fatty acids and vitamins, which help to the health of the cardiovascular system.
It is important to ensure that our food should contain moderate amount of edible
oil with unsaturated fat. The enrichment of the vegetable oils with various
ingredients may contribute to the development of global health care in the
future.
11
CHAPTER 3
3.0 MATERIAL AND METHODS
3.1 COLLECTION OF SAMPLES
Due to being commonly consumed by people commercial soybean oil, melon
seed oil, and groundnut seed oil were purchased from a local market in Eke
Oko, Anambra State. All the oil samples were kept at room temperature until
further analysis.
3.2 HEATING PROCESS
The oil sample was first heated up to 180±1°C for 10 minutes and the analysis
was carried out for the effect of heating on melon seed oil, soybean oil, and
groundnut oil quality.
3.3 USE OF REFRACTOMETER FOR REFRACTIVE INDEX
Refractive index is determined using the refractometer. The refractometer is
cleaned and a smear of the sample is made on the prism and then covered. The
refractive index in nD is read from the calibration through the lens.
3.4 ACID VALUE OR FREE FATTY ACIDS (FFA)
Methods
Mix 25ml diethyl ether with 25ml alcohol and 1ml phenolphthalein solution
(1%) and carefully neutralize with 0.1M NaOH. Dissolve 2g of the oil in the
12
mixed neutral solvent and titrate with aqueous 0.1M NaOH shaking constantly
until a pink colour which persists for 15seconds is obtained.
Calculation:
Acid value = titre value (ml) x 5.61
Sample weight
The FFA figure is usually calculated as oleic acid (1ml of 0.1M potassium
hydroxide = 0.0282g oleic acid), in which case the acid value = 2 x FFA
3.5 IODINE VALUE
Method
Pour the oil into a small beaker, add a small rod and weigh out a suitable
quantity of the sample by difference into a dry glass-stoppered bottle of about
250ml capacity. The approximate weight in g of the oil to be taken can be
calculated by dividing 20 by the highest expected iodine value. Add 10ml of
carbon tetrachloride to the oil and dissolve. Add 20ml of Wijis’ solution insert
the stopper (previously moistened with potassium iodine solution) and allow to
stand in the dark for 30minutes. Add 15ml of potassium iodide solution (10%)
and 100ml of water, mix and titrate with 0.1M thiosulphate solution using starch
as indicator just before the end-point (titration = aml). Carry out a blank at the
same time commencing with 10ml of carbon tetrachloride (titration = bml).
Iodine value = (b-a) x 1.269
Sample weight
13
3.6 SAPONIFICATION VALUE
Method
Weigh 2g of the oil into a conical flask and add exactly 25ml of alcoholic
potassium hydroxide solution. Attach a reflux condenser and heat the flask in a
boiling water bath for 1hr shaking frequently. Add 1ml of phenolphthalein (1%)
solution and titrate hot the excess alkali with 0.5M hydrochloric acid (titration =
aml). Carry out a blank at the same time (titration = bml).
Calculation
Saponification value = (b-a) x 28.05
Sample weight
3.7 PEROXIDE VALUE
Method
Weigh out 1g of oil/fat into a clean dry boiling tube and while still liquid add 1g
powdered potassium iodide and 20ml of solvent mixture ( 2 vol glacial acetic
acid + 1 vol chloroform). Place the tube in boiling water so that the liquid boils
within 30 seconds and allow vigorously for not more than 30 seconds. Pour the
14
contents quickly into a flask containing 20ml potassium iodide solution (5%),
wash out the tube twice with 25ml water and titrate with 0.002M sodium
thiosulphate solution using starch. Perform a blank at the same time.
The peroxide value is often reported as the number of ml of 0.002M sodium
thiosulphate per g of sample. If the value so obtained is multiplied by 2, the
figure equals milliequivalents of peroxide oxygen per kg of sample (mEq/kg)
which has greater international recognition.
3.8 MELTING POINT
Method
Make a smear of the oil on the heating plate of the Fisher-John melting
apparatus and cover with the observation lens. Observe the temperatures at
which the oil just began to melt and when the little smear completely melts
through an inserted thermometer.
Ester value = saponification value – acid value
3.9 DETERMINATION OF VISCOSITY
The viscosity of the oil samples was carried out with the use of viscometer. The
spindle of the viscometer was set with spindle 3 and rpm speed of 65. The
spindle of the viscometer was allowed to be inserted into the oil sample and the
viscosity of the sample measured.
15
3.10 BETA CAROTENE CONTENT
1g of the oil samples each were measured into a 100ml volumetric flask. 5ml of
cyclo-hexane solvent were added to dissolve the oil and make up to mark. The
solution was transferred into 5ml cuvette and the absorbance was measured at
445nm against cyclo-hexane as blank. The carotene content of the oils was
calculated.
Beta carotene (ppm) = V x 383 x (As-Ab)
100 x weight of oil
Where V = volume of oil sample used
As = absorbance of sample
Ab = absorbance of blank
3.11 MOISTURE CONTENT DETERMINATION
The moisture content of oil samples before and after heating was determined by
the Association of Official Analytical Chemists (AOAC, 2004) method. Firstly,
the weight of the previously dried (1 hr at 100°C) crucible with cover was taken
and 5-15 g of sample was placed on it. The samples were dried to constant
weights in an oven at 105°C, cooled in desiccators and weighed. Drying,
cooling and weighing were repeated until the two consecutive weights were the
same. From these weights the percentage of moisture was calculated.
16
3.12 FREE FATTY ACID DETERMINATION
By titrating the alcoholic solution of the oils with an aqueous solution of sodium
hydroxide using phenolphthalein indicator, the free fatty acid concentration was
determined (Aletor et al., 1990). Approximately 10g of the oil was assessed into
the conical flask. 50 ml of alcohol ether mixture in equal volume was added and
it was warmed in a laboratory hotplate stirrer to obtain a homogeneous mixture.
1 mL of phenolphthalein indicator was then added and was titrated with [Link]
NaOH until a fairly pink endpoint was obtained.
FFA as palmitic acid = Titre (mL) of NaOH x N of NaOH x 28.2 Weight of the
sample (g).
3.13 COLOUR DETERMINATION
While the colour is not regarded as an imperative quality feature for the oil, it
has a prodigious impact on consumer acceptance. The colour of oils was
measured the surface colour in terms of L*, a* and b* (Moni et al., 2023) and
using the CIE Hunter Lab system (Color Quest XT, Hunter Associates
Laboratory Inc, USA).
17
CHAPTER FOUR
4.0 RESULT AND DISCUSSION
PHYSIOCHEMICAL COMPOSITION OF GROUNDNUT AND MELON
OIL
TABLE 1
PARAMETER TESTED GROUNDNUT OIL MELON OIL
Acid value (mgKOH/g) 0.65 3.88
Refractive index (nD) 1.693 1.465
Saponification value (mgKOH/g) 194.5 185.0
Iodine value (g/100) 90.2 115.8
Viscosity (mPas-1) 851.00 102.70
Density (g/mL) 0.841 0.883
Peroxide value (meq/kg) 2.21 5.10
Boiling point (C) 205 195
Moisture content % 3.45 0.84
18
4.0 DISCUSSION
4.1 SAPONIFICATION VALUE (SV) OF THE GROUNDNUT AND
MELON OIL
Saponification value (SV) provides very useful information and represent the
optimized quality of cooking oil without the adulteration in the refined oils. The
results as shown in the Table 1, depicts lower SV of 185.0 mg KOH/100g in
melon oil and higher SV of 851 mg KOH/100g in groundnut oil. According to
reported value in literature, an optimized SV should be 182/193mgof
KOH/100g of oil (Alfekaik and Al-Hilfi, 2016). Higher SV indicates higher free
fatty acid and adulteration which is not recommended as healthy cooking oil.
4.2 THE REFRACTIVE INDEX OF THE GROUNDNUT AND
MELON OIL
The refractive index was observed to be 1.693nD in groundnut oil and 1.465nD
in melon oil. The refractive index of melon oil is in close agreement with Bello
et al (2011) for T. occidentalis oil. This value of melon oil is similar to soybean
oil (1.466-1.451) and pure virgin olive oil (1.467) Baig et al., 2022. Refractive
index indicates the possible chances of rancidity development in oil. The higher
the refractive index, the higher is the chances of spoilage during oxidation.
19
Sarkar et al., (2015)
4.3 THE ACID VALUE OF THE GROUNDNUT AND MELON OIL
The acid value of 0.65 mg of KOH/g was obtained in groundnut oil while 3.88
mg KOHg in melon oil. These findings are in close range (0.50-3.00mg/KOH/g
of sample) with the acid value of flaxseed oil from Cold press as reported by
Choo et al., (2007). Acid value is taken as an importance indicator of oxidation
of oil. The acid value is the number of mg of potassium hydroxide required to
neutralize the free acid in 1g of the substance.
4.4 THE VISCOSITY OF THE GROUNDNUT AND MELON OIL
The resistance of the fluid (liquid or gas) to a change in shape, or movement of
neighboring portions relative to one another. From the table 1, the result
indicates that groundnut oil contains+ 851.00mPas-1 while 102.70mPas-1 in
melon oil. Viscosity denotes opposite to flow, the reciprocal of the viscosity is
called the fluidity, a measure of the ease of flow.
CHAPTER FIVE
20
CONCLUSION
Findings from this study showed that, the oil extracted from seeds of groundnut
is a good source of oil due to the oil yield obtained and is capable of meeting
the increasing need for quality and potent oil in industries and domestic
applications based on their physical and chemical properties.
The presented data suggest that melon seeds may constitute useful product with
good nutritional value. The melon seeds contain a high content of crude protein
and oil, e.g. 21% and 22% respectively. The melon kernels had especially high
content: 38% of protein and 52% of oil. The seed oil contains linoleic acid, as a
major fatty acid in 62%. The seeds could be extracted for oil and furthermore
used for edible purposes, and the meal could be used as a meat substitute, and
also for animal and poultry feed or protein production.
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