FAQ

Typical Consumer    Technical     Quality Assurance

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Answers

What is canola oil ?


Canola is a rapeseed variety ( Brassica napus or Brassica campesteris ) which oil component of seed contain less than 5% erucic acid and the solid component less than 30 m mol of glucosinolates per gram of air dry oil free solid (GLC method of the Canadian Grain Commission). 

Rapeseed is mainly grown in Canada, France, Denmark, Poland, UK, India and China. In Western countries, oil for edible use is controlled by legislation at a level of 5% erucic acid (C22 :1) maximum whereas rapeseed oil with high levels of erucic acid (40% minimum ) isfor industrial use only.

Canola oil contains very low levels of saturated fat and high levels of monounsaturated fat. Saturated fats raise cholesterol levels in the blood and promote clogging up of blood arteries leading to heart attack while it has been proven that monounsaturated fat reduces bad cholesterol levels. This leads scientists worldwide to believe that canola oil is one of the healthiest vegetable oil available.

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What is ‘good’ and ‘bad’ cholesterol ?


Cholesterol is distributed throughout the body by lipoproteins (cholesterol carriers) in the blood. Lipoproteins refers to a chemical compound made of fat and protein. There are two kinds, the low density lipoprotein (LDL) which have more fat than protein and high density lipoprotein (HDL) which have more protein than fat.

LDLs carries away cholesterol from the liver through the bloodstream. When excessive LDL levels are registered, they form a hard deposit called plaque, that attaches itself to the walls of the arteries. When an artery of the heart is blocked, a heart attack occurs. If an artery to the brain is clogged, then a stroke occurs. Therefore LDL cholesterol is often referred to as the ‘bad’ cholesterol.

HDLs acts like a little vacuum cleaner and picks up excess fat. HDL carries cholesterol away from the arteries and back to the liver where it is eventually sent to the intestines to be discharged from the body. Therefore HDL cholesterol is also known as the ‘good’ cholesterol because a high HDL level seems to protect against heart attack.

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Is there any cholesterol in canola, soybean, corn or sunflower oil and what are their dietary fat content?

No, these oils are cholesterol free .

Moreover, the amount of saturated fats present are relatively low (refer table 1).

Table 1.   Comparison of dietary fats of various vegetable oils

Fatty acid content normalized to 100 percent (%)

Dietary Fat

 

Saturat- ed Fat

Polyunsaturated Fat

Monounsaturated Fat

Linoleic1

Alpha - Linoleic2
Canola Oil

Sunflower Oil

Corn Oil

Olive Oil

Soya Bean Oil

Palm Oil

Coconut oil

6%

11%

13%

14%

15%

51%

92%

26%

69%

61%

8%

54%

10%

2%

10%

0%

1%

1%

7%

0%

0%

58%

20%

25%

77%

24%

39%

6%


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What are saturated, monounsaturated and polyunsaturated fat ?

What is the significance of these fats to health ?


Basically, all fats or oils (triglycerides) are built up from combinations of fatty acids. These fatty acids combine with one glycerin molecule to form one triglyceride unit. Saturated fatty acid contains the maximum quantity of hydrogen atoms. Saturated fats are solid at room temperature and they are more stable than unsaturated fats.

A fatty acid is unsaturated when there are places on the carbon atom that are unoccupied by hydrogen. When one pair of hydrogen atoms is missing, it is called monounsaturated. When more than one pair of hydrogen atoms is missing, it is called polyunsaturated. Monounsaturated fatty acids which are more stable than polyunsaturated fatty acids will not oxidize as quickly especially during cooking.

Saturated fatty acids is found mainly in palm oil, coconut oil, meat and dairy products. High consumption of saturated fat can raise the cholesterol levels in the blood, clogging up arteries, thus risking a heart attack or stroke.

Polyunsaturated fatty acids is found in vegetable oils such as corn, soybean, sunflower, safflower, cottonseed, as well as most nuts. It can help our bodies remove newly formed cholesterol, thus keeping cholesterol levels low. However, while they lower ‘bad’ LDL cholesterol, they also reduce ‘good’ HDL cholesterol .

Monounsaturated fatty acids, which is abundant in canola and olive oil, reduces cholesterol levels and should make up the bulk of fat in the diet. Medical diet research has proven that monounsaturated fat are healthier than polyunsaturates because they maintain the ‘good’ HDL cholesterol and gets rid of the ‘bad’ LDL cholesterol.

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What are essential fatty acids (EFA) ?


Most fatty acids can be synthesized in the body, but a few polyunsaturated fatty acids cannot be produced at all or are only made in small insufficient amounts. Since the human body cannot function properly without them and must be obtained from food, these are known as essential fatty acids (EFAs).

Essential fatty acids can be divided into two groups :

Omega -3 fatty acids – The two most important types, Eicosapentaenoic acid (EPA) and docosahexanoic acid (DHA) are formed in the body from alpha-linoleic acid . Omega- 3 fatty acid has been found to reduce the process of atherosclerosis (the building up of plaque on the artery walls). Prostaglandins derived from Omega-3 fatty acids regulate the immune system, inhibit blood clotting and have anti-inflammatory effects. It is postulated that multiple sclerosis, a disease characterized by disturbances in the nervous system and myelin breakdown during brain maturation results from deficiency of Omega-3 fatty acids. Canola and soybean oil are good sources.

Omega-6 fatty acids – The most important types are linoleic acid and gamma-linoleic acid (GLA). Linoleic acid is necessary for growth & development of infants, reproduction and essential for healthy skin. Prostaglandins produced from GLA have a beneficial effect on the immune system, circulation and menstrual cycle. Sunflower, corn, soybean and safflower oil are good sources.

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What is the difference between corn oil & soybean oil processing ?

Corn oil is extracted from the corn germ therefore it requires an additional degermination process to separate the germ from the endosperm. The later process is similar with soybean oil processing which involves :

 

1.

Oil Extraction

Historically, many processes were used to recover oil from seeds, but the two most common procedures are expeller pressing and solvent extraction.

Expellers are still used throughout the world on a wide variety of oleaginous materials having high oil contents (e.g. corn germ, sunflower, cottonseed etc.) but their use for soybeans ( having relatively low oil content of 18-20 %) has greatly diminished.

Solvent extraction process to produce crude oil generally consist of three parts

     (i)  preparation of oilseeds – involves cleaning & crushing of oilseeds/ corn germ into flakes to facilitate oil extraction

    (ii)  extraction of oil from the flakes

    (iii) reclamation of solvent from the oil and meal

 

2

Refining of crude oil to produce refined bleached & deodorized oil. This processing step consist of :

Chemical or physical refining - to remove free fatty acids, phosphatides and gums, coloring matter, insoluble matter, settlings and miscellaneous unsaponifiable materials from the triglycerides.

Bleaching – an adsorption treatment to further reduce remaining impurities in refined oil so that the finished oil will be of acceptable color and taste.

Deodorization – the final process step to improve the odor, taste, color and stability of oils by the removal of undesirable substances. This includes FFA, various flavor and odor compounds classified largely as aldehydes, ketones, alcohols , hydrocarbons and compounds formed by heat decomposition of peroxides and pigments.

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How is oil quality measured ?

A number of analytical tests are done in setting up specifications for fats and oils to meet customer’s quality requirements. The most common are as follows:

 

a.

Free Fatty Acids (% FFA)

 

Free fatty acids are fatty acids that are not tied onto a glycerin molecule.

The FFA content in oil can be easily determined by the titration of a known amount of oil sample with NaOH solution (AOCS method Ca 5a-40 ). The result is reported as percentage of free oleic acid.

% FFA indicates the care and control exercised during processing. It is an indication of fresh oil/fat quality. In a well-refined shortening or oil (which does not contain emulsifier) the typical free fatty acid level should be less than 0.05%.

With used oils/fats, it is an indication of the amount of hydrolysis that has taken place. Free fatty acids are the result of reaction of water and fats at frying temperatures. Very high levels of free fatty acids (e.g. about 3-4%) can result in excessive smoking and an unsatisfactory flavor.

Factors that affect the rate of free fatty acid development in frying :

  1. amount of moisture from food that goes into the frying system
  2. Temperature of the frying oil/fat.
  3. presence of burnt food crumbs in the oil/fat
  4. the rate of oil/fat turnover (replacement with fresh frying oil/fat)

a.

Free Fatty Acids (% FFA)

Free fatty acids are fatty acids that are not tied onto a glycerin molecule.

The FFA content in oil can be easily determined by the titration of a known amount of oil sample with NaOH solution (AOCS method Ca 5a-40 ). The result is reported as percentage of free oleic acid.

% FFA indicates the care and control exercised during processing. It is an indication of fresh oil/fat quality. In a well-refined shortening or oil (which does not contain emulsifier) the typical free fatty acid level should be less than 0.05%.

With used oils/fats, it is an indication of the amount of hydrolysis that has taken place. Free fatty acids are the result of reaction of water and fats at frying temperatures. Very high levels of free fatty acids (e.g. about 3-4%) can result in excessive smoking and an unsatisfactory flavor.

Factors that affect the rate of free fatty acid development in frying :

  1. amount of moisture from food that goes into the frying system
  2. Temperature of the frying oil/fat.
  3. presence of burnt food crumbs in the oil/fat
  4. the rate of oil/fat turnover (replacement with fresh frying oil/fat)

 

b. Iodine Value (IV)

The Iodine Value is an index of the number of double bonds in fat. It is a term that can quantify the degree of unsaturation of fat. IV is reported in terms of the grams of iodine that will react with 100g of fat or oil under specified conditions.

Iodine value (AOCS method Cd 1-25 or Wijs Method ) is obtained by reacting fat with known amount of excess halogen, iodine or iodine chloride. The reduction of the excess halogen with KOH and titration with standard sodium thiosulfate using starch solution as free iodine indicator determines the amount of iodine consumed by the fat. The results are expressed as the number of grams of iodine absorbed by 100g of sample, irrespective of the halogen combination used.

Different types of oil have different IV. Therefore IV is a useful means to check for the type of oil and contamination with other types of oil.

 

c. Peroxide Value (PV)

PV is an index to indicate the amount of oxidation a fat has undergone. When oil becomes oxidized, it first develops hydroperoxides. The extent of oxidation is measured by the amount of free iodine the oxidized fat can liberate from KI. The results are expressed as peroxide value (PV) the miliequivalents of iodine formed per kg of fat (AOCS Method Cd 8-53 ). Freshly deodorized oil should have zero PV

PV as a measure of oxidation for unheated fats is useful for determining fat quality after processing and storage. With a fat or oil processed correctly and quickly from good quality oils, the fresh peroxide value will be practically zero . Peroxides will develop to a certain extent during storage before use, with the quantity depending on time, temperature and exposure to light and air.

 

e. Color

Besides having a crystal clear clarity, a good refined oil should have a colour as low as possible. Colour of RBD oil is very critical in the production of mayonnaise and salad oils. Therefore the more colourless the oil is, the better the oil quality.

Color of oil is usually measured by the Lovibond tintometer (AOCS method Cc 13b-45)

Comparing the color of the oil in a glass tube at a standard depth with color of several glass standards does this. Most oils only require a combination of yellow and red glasses. The analyst selects the closest red glass, which is the easiest color to match and then selects a yellow glass with 10 times the color value. The color of measured oil is customarily reported as Red Index / Yellow index.

 

f. Smoke Point

Smoke point is the temperature at which smoking is first detected in a laboratory apparatus protected from drafts and provided with special illumination (AOCS Method Cc 9a-48)

The smoke point of fatty materials is a measure of thermal stability of fats and oils when heated in contact with air. Lower than normal smoke point imply the presence of too much residual non-triglyceride impurities such as FFA, monoglycerides and other volatiles.

 

g. Cold Test

This test is to ensure that all the wax in the oil (especially corn & sunflower oil) have been removed completely in the winterising process. Wax causes the oil to turn cloudy in cold temperature. This is a critical test when oil is exported to countries that experiences winter. Cold winter temperature may cause the wax in the oil to crystallise resulting in a blur appearance. Soybean oil and canola generally do not contain much wax. As such, a positive cold test may indicate that there is a cross contamination of the oil either with corn/ sunflower oil. 

 

h. Shelf Stability Test

This is an accelerated method to determine how stable the RBD oil is during storage. The colour of the RBD oil is measured after incubation in the oven at 100 C for 2 hours. This reading is correlated to the change in colour anticipated afer a few weeks of storage at room temperature. The higher the colour reading is, the less stable the oil is during storage.

 

i. Filter test

This is to check for impurities in the oil. 50 ml of oil is forced through 1 micron filter paper using vacuum suction. The filter paper is then inspected later to see if there are dark stains on it.

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What causes rancidity ?


Off-flavor /odor of fat/oil resulting from the reaction of fat/oil with oxygen in the air is referred to as rancidity. This reaction occurs at the double bonds or points of unsaturation.

Products containing a higher proportion of unsaturated fatty acids are more prone to oxidation. This is owing to the more unstable double bonds; oxygen will more readily react at these points of instability. However proper processing techniques can minimize this tendency.

Factors contributing to the oxidative deterioration of fats and oils

  1. Oxygen (in air )

  2. Amount of surface area of fat that is exposed to air

  3. Light (UV)

  4. Duration of exposure (time)

  5. Temperature (Heat)

  6. Prooxidant metals (e.g copper and iron) which will catalyze oxidation

  7. Presence of antioxidants which retards oxidation

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What are the precautions that needs to be followed to prevent oil oxidation ?

 
Generally, precautions that needs to be followed are as follows :

  1. Limiting atmospheric oxidation by minimizing contact of oil with air (e.g. nitrogen blanketing ) at ambient temperatures and avoiding all contact with oxygen (vacuuming) at very high temperatures e.g. deodorization.

  2. keeping the process time at elevated temperatures as short as possible.

  3. Avoiding, removing and inactivating trace metals (e.g. copper alloys and high temperatures common iron ) with prooxidant effect.

  4. Avoiding exposure of oil to light.

Although these precautions are readily stated, implementing them in commercial operations is not so simple.

Practices to be avoided in transporting or handling the oil includes allowing oil to fall through air and sucking, whipping or bubbling air through the oil.

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What are the factors that causes the deterioration of finished oil quality ?

Factors most likely to affect the quality of finished oils to such an extent that they would require reprocessing (recycling) or be used as a industrial sub-quality product include :
  1. Contamination from atmospheric adulterants
  2. Atmospheric adulteration is avoided by storing the oil in completely closed tanks

  3. Internal contamination from water and soaps
  4. Finished oils held in storage tanks can be contaminated by water leaking from steam or cooling coils. Moisture in the oil can promote hydrolysis, particularly at elevated temperatures resulting in an increase in % FFA content. Proper maintenance of coils is necessary.

  5. Overheating
  6. Overheating of bulk stored oil is undesirable because soaps and pro-oxidant metals are much more active at elevated temperatures. Storage tanks for finished oil should be equipped with automatic temperature controllers to prevent overheating.

     

  7. Exposure to air and oxygen
  8. Oxidation has the most detrimental effect on the quality of finished oils held in bulk storage. The usual procedure involves nitrogen blanketing (i.e. replacing oxygen with nitrogen ) where the finished oil is delivered from the deodorizer to the storage tank under a complete nitrogen blanket. The nitrogen blanket is maintained by a pressure system controlled by a regulator

    Resistance to oxidation : Crude oil > Partially processed oil > Finished oil

    Oil stores best as crude oil. Refined bleached & deodorized oil (finished oil) is more susceptible to oxidation than other stages in processing. For this reason, the finished oil should be stored only for brief periods.

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How does Soon Soon assure the quality of oils ?

Soon-Soon is committed to assure the quality of oils/oil products to meet customer requirements by performing quality evaluation on every process step involving:
  1. Incoming Raw material - oilseeds & packing material
  2. Storage of Raw Material
  3. Storage of refined oil
  4. On line processing (QC)
  5. Delivery – quality testing, tanker inspection and issuing of COA
  6. After sales – A team of QA Inspectors doing after sales ‘Quality Survey’ at Supermarkets.
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Facility Function / Tests conducted
1. Central lab

 

Chemical Analysis - PV, FFA, Moisture

Physical Analysis - Color, Filter Test, Cold test, Clarity,

Shelf Stability Test

2. Instrumentation Lab NIR- Iodine value, GC – Fatty Acid Content, Rancimat- OSI

AAS –Heavy metal analysis, NMR –Solid Fat Content

3. Microbiology lab Total Aflatoxin Count for incoming oilseed
4. Food Research Center Intensive R & D programs
5. Pilot Plant Process investigation & new product development
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