48 CHANGES OF CONDITION.
tion has been obtained, the ether can be driven off completely and
air introduced to oxidize the excess phosphorus, without injury
to the gold colloid (hydrosol). This preparation of colloidal gold
solution is very sensitive to external conditions; it is not possible
to produce equally good solutions in all laboratories.
- Colloidal Gold by Reduction with Carbon Monoxide. Prepare
carbon monoxide by heating oxalic acid crystals with concentrated
sulfuric acid, and passing the gas through sodium hydroxide solu-
tion to remove carbon dioxide. Pass a slow stream of the carbon
monoxide into 120 cc. of 0.03% chlorauric acid. There is pro-
duced a violet color which changes to violet-red and later to a dark
red. Do not carry the reduction too far, as the solution will then
assume a permanent violet color.
- Colloidal Gold by Reduction with the Hydrogen Flame.
1
It is
easy to prepare a colloidal gold solution by merely directing a
pointed hydrogen flame, 1 to 2 cm. long, against a 0.03% solution
of chlorauric acid contained in a wide, porcelain dish. After
about five minutes the solution begins to be colored; soon a rich
red color is produced. Occasional stirring hastens the formation
of the colloidal gold.
Use a gold solution prepared by any one of these methods in the
following experiments.
I. Synthesis of Purple of Cassius. From a mixture of colloidal
stannic oxide and colloidal gold, the gold-stannic oxide adsorption
compound is precipitated on the addition of electrolytes. In order
to prepare the colloidal stannic acid solution, allow 5 cc. of tin
tetrachloride (No. 50) to become hydrolyzed by the addition of
150 to 200 cc. of water, and pour this solution into 500 cc. of
water to which a few drops of ammonia have been added. Dialyze
the clear mixture for five days (cf. No. 21), changing the outside
water two or three times daily, until it shows no test for chlorides.
If during this process a hydrogel separates in the dialyzing tube,
it may be peptonized (see p. 40) in a beaker by the addition of
about three drops of ammonia, whereupon, after a time, the jelly
will go over into a perfectly clear hydrosol. A mixture of this
hydrosol with an equal volume of gold solution remains unchanged,
but on addition of a salt (ammonium chloride) a beautiful deep-
(^1) J. Donau, Monatsh. 34, 949 (1913). Colloidal solutions of silver, platinum
and molybdenum blue can be prepared by this method.