Oil Analysis
Oil Analysis
Oil Analysis
Oil analysis refers to the analysis of oil or fats to determine the properties of
oil, which are important in different purposes. These values are important in
different circumstances. We have to know the number of instaurations or double
or triple bonds in an oil or fat while using in chemical reactions or industrial
purposes. Iodine value indicates the number of double/triple bonds. On the other
hand, if we want to produce soap, for best production we have to select suitable
oil, which will produce more soap & is easy to collect. For this purpose we have
to know the saponification values of different oils. We must know the acidity or
alkalinity of oil while using it in chemical reactions, even in hair care. So we will
use some experimental way of determining the properties of oil. These
experiments are DETERMINATION OF IODINE VALUE (IV) OF OILS
DETERMINATION OF SAPONIFICATION VALUE (SV) OF OILS
DETERMINATION OF ACID VALUE & BASE VALUE OF OILS.
Iodine Value- Iodine value can be defined as the amount of iodine in grams
reacted with 100 grams of a oil or fat under saturated condition, and is measure
of the instaurations present. Iodine value (IV) is a measure of the total number of
double bonds present in fats and oils. It is generally expressed in terms of
"number of grams of iodine that will react with the double bonds in 100 grams of
fats or oils".
Oils have double bonds & iodine replaces the pai () bonds and produce iodides.
C C
+ I2
I
I
CC
I
I
This amount of iodine reacted with oil sample is the iodine value. Higher the
iodine value indicates the higher instauration. So in case of edible oils with high
iodine value are usually less stable and more susceptible to oxidation and a
better quality of oil but in case of coconut hair oil this means rather different.
C C
+ IBr
I
I
CC
I
I
Br2
Br2
I2
KBr
Then this remaining Iodine is titrated with standard Na 2S2O3 solution. This
titration is a iodometric titration. There is still excess iodide in the sample, and it combines
with the iodine to form tri-iodide ( I-3):
I2(aq)
I-(aq)
I-3 (aq)
Finally, the tri-iodide is reacted in yet another oxidation-reduction step back to iodide, in the
presence of thiosulphate ion (S2O3-2), with the formation of tetrathionate ion (S 4O6-2):
I-3(aq)
S2O3-2(aq)
3I-(aq)
S4O6-2(aq)
Useful Chemicals:
Experimental Data:
Table 1: Standardization of Sodium thiosulphate (Na 2S2O3) solution with
standard potassium dichromate (K2Cr2O7) solution:
No. of
Volume of
Burette reading
Volume of
Average
Obs.
K2Cr2O7 (ml) Initial (ml) Final (ml)
Na2S2O3
volume of
(ml)
Na2S2O3 (ml)
1
10
0.2
15.1
14.9
14.933
2
10
15.1
30.0
14.9
3
10
30.0
45.0
15.0
Sample (Parachute Coconut Oil) Oil taken, W = 0.728 gram
No. of
Obs.
1
Calculations:
Weight of the sample Lily Coconut Oil, W = 0.728 gm
Strength of Na2S2O3, N =
0.1 10
N
14.933
= 0.0676 N
Volume of Na2S2O3 in blank titration, B = 32.7 ml
Volume of Na2S2O3 in sample titration, A = 11.5 ml
12.7 B A N
Iodine Value, IV =
W
12.7 33.5 18.20 0.0676
=
0.728
= 18.043
Result:
The Iodine Value (IV) Of Sample Lily Coconut Oil = 18.043
Volume of
Na2S2O3 (ml)
18.20
Volume of
Na2S2O3 (ml)
33.50
Discussion:
Here while determining iodine value Iodine was not added directly. It was added
as Ian iodine reagent henus solution where iodine is present as IBr. If we use
iodine directly the reaction would not be done easily as the reaction mechanism
does not support iodine to directly with the bonds. I 2is not a polar molecule, but
the bonds reacts easily with polar molecules. On the other hand the IBr
molecule is polar which reacts easily with unsaturated oils & fats.
The measure of such instauration is more important in case of edible
oils. So in case of edible oil high iodine value is more favorable than
that of a lower one.
To perform the experiment more accurately we must have to shake the
reagents mixture for about an hour otherwise the saturation may not
be occurred. And some disappearances have to be observed from the
standard value.
Objective:
The objective of this experiment is to determine the saponification value of oils
or fats. The saponification value is usually used, where in analytical work the
saponification equivalent is more useful.
KOH =
soap
water
Total reaction:
CH2OCOC17H35
|
CHOCOC17H35
|
CH2OCOC17H35
Stearin
potassium stearate
+ 3KOH
CH2OH
|
CHOH
|
CH2OH
3C17H35COOK
glycerol
will give the value of HCl solution required to neutralize the KOH, which was
involved to saponify the oil if in both case the amount of solution of KOH is same.
Indicator- In the neutralization titration of excess KOH with standard HCl
we used phenolphthalein indicator. This indicator changes its color in
neutralization reactions in pH range 8.3 to 10.
Chemicals:
Alkoholic KOH
HCl, 0.5N
Phenolphthalein Indicator
Experimental Data:
Weight of sample: (Soya bin oil) = 1.121 gm
Table 1: Data for blank titration:
No. of
Vol. of alcoholic
Burette Reading
Obs.
KOH (ml)
Initial (ml)
Final (ml)
1
20
0.10
17.6 0
Table 2: Data for titration of excess KOH with HCl for Soya bin oil:
No. of
Vol. of alcoholic
Burette Reading
Volume of HCl (ml)
Obs.
KOH (ml)
Initial (ml)
Final (ml)
1
20
18.10
27.70
9.60
Calculation:
Here,
Weight of the sample Lily coconut oil, W = 1.121 gm
Normality of HCl, N = 0.532 N
Vol. of HCl in ml use in the titration with sample, V =9.60 ml
Vol. of HCl in ml use in the blank titration, V o = 17.50 ml
Result:
The Saponification Value (SV) Of Sample: (Soya bin Oil) = 210.33
Discussion:
The saponification value is inversely proportional to the molecular
weight of the fatty acids obtained from esters.
To do the experiment perfectly we should reflux the reagents
mixture in water bath for about 24h otherwise we may have some
disappearances. There may some disappearances due not to
hydrolyze the fat properly because we spent only half an hour
instead of 24 hour.
The solution of HCl must be standardized properly before titration
carried out.
From the experiment we can know how to measure the purity of
oils or
fats.
This saponification value must vary from source to source of oil and
fat such as the saponification value of edible pure oil, pure fat,
and hair oil must be different.
Figure: Phenolphthalein
In a typical procedure, a known amount of sample dissolved in organic
solvent is titrated with a solution of potassium hydroxide with known
concentration and with phenolphthalein as a color indicator.
Chemicals:
KOH solution
Phenolphthalein Indicator
Experimental Data:
No.
Obs.
1
Calculation:
Here,
Weight of the sample Lily coconut oil, W = 0.927 gm
Normality of KOH solution, N = 0.01 N
Volume of KOH in ml, V = 2.80 ml
Result:
The Acid Value (AV) Of Sample Lily Coconut Oil = 1.694
Discussion:
BIBLIOGRAPY:
VOGELS
TEXTBOOK OF QUANTATIVE CHEMICAL ANALYSIS
-J MENDHAM, R C DENNEY, J D BARNES, M J K THOMAS.
GENERAL CHEMISTRY
-EBBINGS.
ESSENTIALS OF PHYSICAL CHEMISTRY
-B S BHAL, G D TULI, ARUN BHAL.