Soap-Making Manual: A Practical Handbook on the Raw Materials, Their Manipulation, Analysis and Control in the Modern Soap Plant.Thomssen, Edgar George
Science
Soap-Making Manual: A Practical Handbook on the Raw Materials, Their Manipulation, Analysis and Control in the Modern Soap Plant.
Thomssen, Edgar George
Soap
To make the determination about 30 grams of fat are roughly weighed in a
metal dish and 30-40 cubic centimeters of a 30 per cent. (36 degs.
Baume) solution of sodium hydroxide, together with 30-40 cubic
centimeters of alcohol, denatured alcohol will do, are added and the
mass heated until saponified. Heat over a low flame or over an asbestos
plate until the soap thus formed is dry, constantly stirring the
contents of the dish to prevent burning. The dried soap is then
dissolved in about 1000 cubic centimeters of water, being certain that
all the alcohol has been expelled by boiling the soap solution for about
half an hour. When the soap is in solution add sufficient sulphuric acid
to decompose the soap, approximately 100 cubic centimeters of 25 degs.
Baume sulphuric acid, and boil until the fatty acids form a clear layer
on top of the liquid. A few pieces of pumice stone put into the mixture
will prevent the bumping caused by boiling. Siphon off the water from
the bottom of the dish and wash the fatty acids with boiling water until
free from sulphuric acid. Collect the fatty acids in a small casserole
or beaker and dry them over a steam bath or drying oven at 110 degs.
Centigrade. When the fatty acids are dry, cool them to about 10 degs.
above the titer expected and transfer them to a titer tube or short test
tube which is firmly supported by a cork in the opening of a salt mouth
bottle. Hang the thermometer by a cord from above the supported tube so
it reaches close to the bottom when in the titer tube containing the
fatty acids and so that it may be used as a stirrer. Stir the mass
rather slowly, closely noting the temperature. The temperature will
gradually fall during the stirring operation and finally remain
stationary for half a minute or so then rise from 0.1 to 0.5 degs. The
highest point to which the mercury rises after having been stationary is
taken as the reading of the titer.
DETERMINATION OF UNSAPONIFIABLE MATTER.
In order to determine the unsaponifiable matter in fats and oils they
are first saponified, then the unsaponifiable, which consists mainly of
hydrocarbons and the higher alcohols cholesterol or phytosterol, is
extracted with ether or petroleum ether, the ether evaporated and the
residue weighed as unsaponifiable.
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