Poisons, Their Effects and Detection: A Manual for the Use of Analytical Chemists and ExpertsBlyth, Alexander Wynter
Science
Poisons, Their Effects and Detection: A Manual for the Use of Analytical Chemists and Experts
Blyth, Alexander Wynter
Poisons
§ 149. Benzene is separated from liquids by distillation, and may be
recognised by its odour, and by the properties described at p. 130.
The best process of identification, perhaps, is to purify and
convert it into nitro-benzene, and then into aniline, in the
following manner:--
1. =Purification.=--The liquid is agitated with a solution of
caustic soda; this dissolves out of the benzene any bodies of an
acid character, such as phenol, &c. The purified liquid should again
be distilled, collecting that portion of the distillate which passes
over between 65° and 100°; directly the thermometer attains nearly
the 100°, the distillation should be stopped. The distillate, which
contains all the benzene present, is next shaken with concentrated
sulphuric acid in the cold; this will dissolve out all the
hydrocarbons of the ethylene and acetylene series. On removing the
layer of benzene from the acid, it must be again shaken up with
dilute soda, so as to remove any trace of acid. The benzene is, by
this rather complicated series of operations, obtained in a very
fair state of purity, and may be converted into nitro-benzene, as
follows:--
2. =Conversion into Nitro-Benzene.=--The oily liquid is placed in a
flask, and treated with four times its volume of fuming nitric acid.
The flask must be furnished with an upright condenser; a vigorous
action mostly takes place without the application of heat, but if
this does not occur, the flask may be warmed for a few minutes.
After the conversion is over, the liquid, while still warm, must be
transferred into a burette furnished with a glass tap, or to a
separating funnel, and all, except the top layer, run into cold
water; if benzene was originally present, either oily drops of
nitro-benzene will fall, or if the benzene was only in small
quantity, a fine precipitate will gradually settle down to the
bottom of the vessel, and a distinct bitter-almond smell be
observed; but, if there be no benzene in the original liquid, and,
consequently, no nitro-benzene formed, no such appearance will be
observed.
3. =Conversion into Aniline.=--The nitro-benzene may itself be
identified by collecting it on a wet filter, dissolving it off the
filter by alcohol, acidifying the alcoholic solution by hydrochloric
acid, and then boiling it for some time with metallic zinc. In this
way aniline is formed by reduction. On neutralising and diluting the
liquid, and cautiously adding a little clear solution of
bleaching-powder, a blue or purple colour passing to brown is in a
little time produced.
3. TERPENES--ESSENTIAL OILS--OIL OF TURPENTINE.
§ 150. The terpenes are hydrocarbons of the general formula
C_{n}H_{2n-4}. The natural terpenes are divided into three
classes:--
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