Chemistry Investigation Project
Chemistry Investigation Project
subheadings
soap:
introduction
fat in soap
preparation of soap
2 objective
3 theory
4 observation
5 Apparatus Requirements
6 Chemical Requirements
8 Procedure
9 observation
10 results
OBJECTIVE:
To compare the foaming capacity of various soaps.
Theory
The foaming capacity of soap depends upon the nature of
the soap and its concentration. This may be compared by
shaking equal volumes of solutions of different samples
having the same concentration with same force for the
same amount of time. The solutions are then allowed to
stand when the foam produced during shaking disappears
gradually. The time taken for the foam to disappear in
each sample is determined. The longer the time taken for
the disappearance of the foam for the given sample of
soap, greater is its foaming capacity or cleansing action.
Apparatus Requirements:
Five 100ml conical flasks, five test tubes, 100ml
measuring cylinder, test tube stand, weighing machine,
stop watch.
Chemical Requirements:
Five different soap samples, distilled water, tap
water.
Procedure
1.Take five 100ml conical flasks and number them 1,2,3,4,5. Put 16ml of
water in each flask and add 8 grams of soap.
2.Warm the contents to get a solution.
3.Take five test tubes; add 1ml of soap solution to 3ml of water.
Repeat the process for each soap solution in different test tubes
4. Close the mouth of the test tube and shake vigorously for a minute.
Do the same for all test tubes and with equal force.
From this experiment, we can infer that Santoor has the highest
foaming capacity, in other words, highest cleaning capacity. Lux,
on the other hand is found to have taken the least amount of
time for the disappearance of foam produced and thus is said
to be having the least foaming capacity and cleansing capacity.
The tests show negative results for the presence of the salts
causing hardness in water. The water used does not contain salts
of Ca2+ and Mg2+. The tap water provided is soft and thus, the
experimental results and values hold good for distilled water and
tap water.
effect of adding sodium
carbonate
Soaps are sodium or potassium salts of higher fatty acids like stearic, palmitic
and oleic acids can be either saturated or unsaturated. They contain a long
hydrocarbon chain of about 10-20 carbon with one carboxylic acid group as the
functional group. A soap molecule a tadpole shaped structure, whose ends have
different polarities. At one end is the long hydrocarbon chain that is non- polar
and hydrophobic, i.e., insoluble in water but oil soluble. At the other end is the
short polar carboxylate ion which is hydrophilic i.e., water soluble but insoluble
in oil and grease. Long Hydrocarbon Chain contain Hydrophobic and Hydrophilic
end. When soap is shaken with water it becomes a soap solution that is colloidal
in nature. Agitating it tends to concentrate the solution on the surface and
causes foaming. This helps the soap molecules make a unimolecular film on the
surface of water and to penetrate the fabric. The long non-polar end of a soap
molecule that are hydrophobic, gravitate towards and surround the dirt (fat or
oil with dust absorbed in it). The short polar end containing the carboxylate ion,
face the water away from the dirt. A number of soap molecules surround or
encircle dirt and grease in a clustered structure called ‘micelles’, which encircles
such particles and emulsify them. Cleansing action of soaps decreases in hard
water. Hard water contains Calcium and magnesium ions which react with sodium
carbonate to produce insoluble carbonates of higher fatty acids. This hardness
can be removed by addition of Sodium Carbonate
commercial
preparation of soap
The most popular soap making process today is the cold process method,
where fats such as olive oil react with strong alkaline solution, while some
soapers use the historical hot process. Handmade soap differs from
industrial soap in that, usually, an excess of fat is sometimes used to
consume the alkali (super fatting), and in that the glycerine is not
removed, leaving a naturally moisturizing soap and not pure detergent.
Often, emollients such as jojoba oil or Shea butter are added ‘at trace’
(the point at which the saponification process is sufficiently advanced
that the soap has begun to thicken), after most of the oils have
saponified, so that they remain unreacted in the finished soap.
Soap is derived from either vegetable or animal fats. Sodium
Tallowate, a common ingredient in much soap, is derived from
rendered beef fat. Soap can also be made of vegetable oils, such as
palm oil, and the product is typically softer. An array of specifiable
oils and fats are used in the process such as olive, coconut, palm,
cocoa butter to provide different qualities. For example, olive oil
provides mildness in soap; coconut oil provides lots of lather; while
coconut and palm oils provide hardness. Sometimes castor oil can also
be used as an ebullient. Smaller amounts of unsaponifiable oils and
fats that do not yield soap are sometimes added for further
benefits.
preparations
of soap
HOT AND COLD PROCESS
about
soaps
Soap is a common term for a number of related compounds used as of washing clothes or
bathing. Soaps are sodium or potassium salts of higher fatty acids such as stearic acid (C17 H35
COOH), palmittic acid (C15 H31 COOH) and oleic acid (C17H35 COOH) they have the general
formula RCOONa and R COONa. Soap is produced by a saponification or basic hydrolysis
reaction of a fat or oil. Currently sodium carbonate or sodium hydroxide is used to neutralize
the fatty acid and convert it to the salt..
Although the reaction is shown as one step reaction, it is in fact two steps. The net effect as
that the ester bonds all broken. The glycerol turns back into an alcohol. The fatty acid is
turned into a salt due to the presence of a basic solution of NaoH. In the carboxyl group, one
oxygen now has a negative charge that attacts the positive sodium ion. A molecule of soap
consists of two parts.
When present in water, these substances arrange themselves in the spherical structure in
such a manner that their hydrophobic parts are present towards the centre, while the
hydrophilic parts are pointing towards the outside (as shown in the given figure). This is
known as micelles formation.
These molecules are arranged radially with the hydrocarbon or non-polar part towards
the centre and the periphery.
The hydrocarbon tail is made of the long carbon chain and it is nonpolar.
Since it is a carbon chain it doesn’t have the affinity towards the water.
Therefore, it is also called the hydrophobic end (or water-hating or repelling).
It is readily soluble in oil and grease The sops are fatty acid derivatives
therefore one end of the hydrocarbon chain bonded to the carboxylic acid
therefore the negatively charged head is polar. It has a great affinity towards
the water. It is also known as the hydrophilic end (water-loving). It is readily
soluble in water.
Additional information:
In aqueous solution, water molecules are polar thus they
surround the head of the molecule and repel the hydrocarbon
tail. Therefore when soap or detergent is dissolved in water,
the molecules associate to form a cluster of molecules called
as the micelles as shown below,
SOAP