We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 2
BABCOCK UNIVERSITY
COLLEGE OF HEALTH AND MEDICAL SCIENCES
BENJAMIN S. CARSON (SNR.) SCHOOL OF MEDICINE DEPARTMENT OF BIOCHEMISTRY
312 PRACTICAL (NUTRITION AND FOOD BIOCHEMISTRY)
2ND SEMESTER, 2020/2021 SESSION VENUE: Biochemistry Laboratory LECTURER: ADEWOLE O and OGBONNAYA F.C.
DETERMINATION OF SAPONIFICATION VALUE
Saponification is the hydrolysis of fats or oils under basic conditions to afford glycerol and the salt of the corresponding fatty acid. Saponification literally means "soap making". It is important to the industrial user to know the amount of free fatty acid present, since this determines in large measure the refining loss. The amount of free fatty acid is estimated by determining the quantity of alkali that must be added to the fat to render it neutral. This is done by warming a known amount of the fat with strong aqueous caustic soda solution, which converts the free fatty acid into soap. This soap is then removed and the amount of fat remaining is then determined. The loss is estimated by subtracting this amount from the amount of fat originally taken for the test. The saponification number is the number of milligrams of potassium hydroxide required to neutralize the fatty acids resulting from the complete hydrolysis of 1g of fat. It gives information concerning the character of the fatty acids of the fat, the longer the carbon chain, the less acid is liberated per gram of fat hydrolysed. It is also considered as a measure of the average molecular weight (or chain length) of all the fatty acids present. The long chain fatty acids found in fats have low saponification value because they have a relatively fewer number of carboxylic functional groups per unit mass of the fat and therefore high molecular weight.
DETERMINATION OF SAPONIFICATION VALUE OF OIL SAMPLES
Aim: To determine the saponification value of fresh and rancid oil samples. Materials: Burette, conical flask, hot plate, funnel, oil samples (rancid and fresh oil), retort stand, 0.5M KOH, 0.5M HCL, fat solvent (diethyl ether and ethanol in the ratio 1:1), phenolphthalein indicator, dropping pipette. Procedure: Place 1ml of each oil sample in different conical flasks. Add 3ml of fat solvent and 20ml of KOH to each. Boil solution on hot plate for one minute. 1 Allow to cool, then add 2 drops of phenolphthalein. Titrate each against 0.5M HCL and record the titre value for each. Repeat procedure for blank test but without addition of any oil sample (i.e. exclude step 1). Calculate the saponification value for each oil sample using the following formula: Saponification value (mg/ml of KOH) = (a–b) ml X Molarity of HCL X Molar mass of base Volume of oil sample Where: a = Titre value of blank b = Titre value of oil sample Molarity of HCL = 0.5M Molar mass of base = 56.1