Legal Chemistry: A Guide to the Detection of Poisons, Examination of Tea, Stains, Etc., as Applied to Chemical Jurisprudence — John Shaqi
Legal Chemistry: A Guide to the Detection of Poisons, Examination of Tea, Stains, Etc., as Applied to Chemical JurisprudenceNaquet, Alfred
Science
Legal Chemistry: A Guide to the Detection of Poisons, Examination of Tea, Stains, Etc., as Applied to Chemical Jurisprudence
Naquet, Alfred
Chemistry, Forensic; Poisons
The solution is placed in a retort provided with a receiver and
distilled until the residual fluid assumes a pasty consistence: the
operation is then discontinued. If hydrochloric acid be present in the
materials under examination, the distillate will have an acid reaction,
and, upon addition of solution of nitrate of silver, a white
precipitate, which is easily soluble in ammonia but insoluble in nitric
acid and in short possesses all the properties of chloride of silver,
will be formed.
NITRIC ACID.
The distillate, obtained as in the preceding process, is neutralized by
the addition of potassa or soda, and evaporated to dryness. The residue
is mixed with copper filings, and introduced into a glass tube closed at
one end and provided at the other with a cork through which a
delivery-tube passes. Sulphuric acid is then added to the mixture, the
cork inserted, the tube heated, and the evolved vapors conducted into a
solution of protosulphate of iron. The latter solution acquires a brown
coloration which, upon addition of sulphuric acid, changes to a violet,
if nitric acid be present. Upon conducting the disengaged gas into a
solution of narcotine, the latter acquires a beautiful red color.
Another portion of the residue should deflagrate when saturated with an
alkali and projected upon live coals.
SULPHURIC ACID.
In order to detect this acid, the solution obtained by treating the
organs with water is not distilled but is concentrated to one-sixth of
its original volume, and then agitated with ether for about ten minutes.
By this treatment the ether takes up the free sulphuric acid, but not
the acid sulphates present. After ten minutes contact, the ether is
decanted and allowed to spontaneously evaporate. Upon treating the
residue, which contains the free sulphuric acid and fatty substances,
with water, a solution containing only the sulphuric acid is obtained.
Nitrate of baryta is then added to a portion of the fluid: in presence
of sulphuric acid, a white precipitate, insoluble in acids, is produced.
If this is heated on charcoal before the blow-pipe, a mass is formed,
which, when moistened with hydrochloric acid and placed upon a clean
silver coin, produces a black spot on the metal. Another portion of the
solution is mixed with copper and the mixture evaporated in a tube
closed at one end: sulphurous acid is evolved towards the end of the
operation. This gas is detected by allowing it to pass over paper
saturated with a mixture of iodic acid and starch; a blue coloration is
produced which, owing to the transformation of the iodine set free into
hydriodic acid, subsequently disappears. (We have never been able to
effect the disengagement of sulphurous acid spoken of above when an
exceedingly dilute sulphuric acid was used, even upon evaporating the
mixture to dryness, notwithstanding Orfila's statement that the reaction
occurs very readily.)
PHOSPHORIC ACID.
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