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
_c._ OXALIC ACID.--The third portion of the residue is heated with
sulphuric acid, and the evolved gas carefully collected. It should then
be confirmed by an elementary analysis that the gas consists of equal
volumes of carbonic oxide and carbonic acid. This test is not
conclusive; it is also necessary to ascertain if the precipitate
produced by the addition of a baryta solution (_vide_: under portion
_B._) produces the same reaction, inasmuch as other organic bodies could
give rise to carbonic oxide and carbonic acid, and the danger of both
admitting the presence of oxalic acid, when it is absent, and omitting
its detection, in case it is present, would be incurred.
_d._ ACETIC AND FORMIC ACIDS.--The fourth portion of the residue is
distilled with dilute sulphuric acid. After determining that a small
portion, previously neutralized with a base, acquires a red color, upon
addition of a solution of a persalt of iron, the distillate is divided
into two parts. One portion is treated with bichloride of mercury: if
_formic acid_ be present, metallic mercury is formed, with evolution of
carbonic acid which produces turbidity in lime-water. The remaining
portion of the fluid is digested, in the cold, with an excess of
litharge: in presence of _acetic acid_, a soluble basic salt of lead,
possessing an alkaline reaction, is produced.
PORTION B.--The second portion of the solution is supersaturated with
nitric acid, and this neutralized by addition of a slight excess of
ammonia. The ammonia is then expelled by boiling the fluid, and a
solution of nitrate of baryta added. If a _precipitate_ forms, it is
collected and subsequently examined for sulphuric, phosphoric, oxalic
and boric acids as directed below. The _filtrate_ is preserved and
tested for hydrochloric, hydrobromic and hydriodic acids.
_a._ OXALIC ACID.--A portion of the precipitate produced by the addition
of nitrate of baryta is submitted to the test mentioned under the
treatment of portion _A_.
_b._ SULPHURIC ACID.--If an insoluble residue remains upon treating the
remainder of the precipitate with dilute hydrochloric acid, it consists
of sulphate of baryta and indicates the presence of _sulphuric acid_.
_c._ PHOSPHORIC ACID.--An excess of solution of alum and ammonia is
added to the portion of the precipitate dissolved in hydrochloric acid.
If phosphoric acid be present, insoluble phosphate of alumina is
precipitated. This is brought upon a filter: the _filtrate_ being
preserved and subsequently examined for boric acid. Upon boiling the
precipitate with solution of silicate of potassa, silicate of alumina is
thrown down, and phosphate of potassa remains in solution. Chloride of
ammonia is now added to the liquid--in order to eliminate the excess of
silica from the silicate--and the solution filtered. The _filtrate_ is
then tested for phosphates, by means of molybdate of ammonia (_vide_:
_detection of phosphoric acid_, p. 48).
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