Food Adulteration and Its Detection: With photomicrographic plates and a bibliographical appendixBattershall, Jesse P. (Jesse Park)
Science
Food Adulteration and Its Detection: With photomicrographic plates and a bibliographical appendix
Battershall, Jesse P. (Jesse Park)
Food adulteration and inspection; Food adulteration and inspection -- United States
_Free Tartaric Acid and Potassium Bitartrate._--In the presence
of a small amount of free acids, the detection of a considerable
proportion of free tartaric acid may fairly be considered as strong
evidence that the wine is artificial. Nessler recommends the following
qualitative test:--20 c.c. of the sample are repeatedly shaken with
a little freshly prepared and finely ground cream of tartar. After
standing one hour, the solution is filtered, 3 or 4 drops of a 20
per cent. solution of potassium acetate are added, and the mixture
is allowed to remain at rest for twelve hours, when, in presence of
free tartaric acid, a precipitation will take place. The quantitative
estimation of free tartaric acid and potassium bitartrate is made
by Berthelot’s method, as follows:--Separate portions of the wine
(20 c.c. each) are introduced into two flasks, a few drops of 20 per
cent. solution of potassium acetate being added to the second flask.
200 c.c. of a mixture of equal parts of alcohol and ether are then
added to both flasks, their contents repeatedly shaken and finally
set aside for eighteen hours at a temperature between 0° and 10°. The
separated precipitates are now removed by filtration, washed with the
ether-alcohol mixture, and then titrated with 1/10th normal alkali
solution. That formed in the first flask corresponds to the potassium
bitartrate originally contained in the wine; the second represents the
total tartaric acid present. The addition of a small quantity of clean
sand will assist in the separation of the precipitates.
_Malic Acid._--A slight excess of lime-water is added to 100 c.c. of
the wine, and, after standing for some time the solution is filtered,
concentrated by evaporation to one-half its original volume, and
treated with an excess of absolute alcohol. The resulting precipitate
(consisting of calcium malate and sulphate) is collected upon a filter,
dried and then incinerated. The proportion of malic acid contained
is now estimated by volumetrically determining the amount of calcium
carbonate present by means of a normal acid solution: 1 part of calcium
carbonate represents 1·34 parts of malic acid (C_{4}H_{6}O_{5}).
_Tannic Acid._--10 c.c. of the sample are taken, the free acids
present neutralised with normal alkali solution, and a few drops of
concentrated sodium acetate solution (40 per cent.) added. A solution
of ferric chloride (10 per cent.) is then added, drop by drop,
carefully avoiding an excess. A single drop of the iron solution
represents 0·05 per cent. of tannic acid. The method of tannin
determination described under Tea (see p. 22) can also be applied.
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