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dissolve it in as little HCl as possible, and evaporate it almost to dryness. On adding water to this solution, a precipitate of Biocl at once forms, which is insoluble in tartaric acid (compare corresponding reaction with antimony, 74, 4). Solutions of bismuth salts containing much free acid do not give this reaction with H2O until the excess of acid has been expelled by evaporation.

4. K,Cr0, produces a yellow precipitate of Big(CrO4)3, soluble in HNO3, and insoluble in NaHO. (Compare reaction for lead, 65, 3.)

5. Heated on charcoal with NaHCO, in the reducing flame of the blow-pipe, yields brittle metallic globules; also a slight yellow incrustation of oxide on the charcoal.

70. COPPER. Cu, c.w. 63.5.

1. H,S produces a black precipitate of CuS, soluble in HNO3, but insoluble in KHS, and only slightly soluble in (NH4)2S2. CuS is also dissolved by KCN, but is insoluble in hot dilute H2SO4.

2. KHO produces a pale blue precipitate of Cu(HO), insoluble in excess of the precipitant. If the KHO be added in excess and the mixture boiled, the precipitate becomes black and loses water.

3. (NH4)HO produces, when added in small quantities, a greenish blue precipitate of a basic salt, soluble in excess to a dark blue solution, which consists of a double basic salt of copper and ammonium.

4. K Fe(CN). produces a brown precipitate of Cu, Fe(CN), insoluble in dilute acids, but decomposed by KHO.

5. Fe precipitates copper in the metallic state, from its solutions, especially in presence of a little free acid. The iron ought to be bright and clean.

6. Zn also precipitates copper solutions. If a solution of copper containing a few drops of HCl be placed in a platinum capsule, and a fragment of zinc added, the copper will be precipitated on the platinum as a red coating.

7. Compounds of copper, when heated in the Bunsen lamp flame, impart a green colour to it, especially after addition of AgCl.

8. Mixed with NaHCO3 + KCN and heated on charcoal before the reducing blow-pipe flame, yields bright red metallic particles, soluble in HNO3, and giving a deep blue solution on adding (NH4)HO.

71. CADMIUM. Cd, C.W. 112.

1. H S produces a yellow precipitate of CdS, soluble in HNO3, but insoluble in KHS, in (NH4),S, and in KCN. CdS is dissolved by hot dilute H2SO4. (Compare reaction for copper, 70, 1.)

2. KHO produces a white precipitate of Ca(HO)2, insoluble in an excess of the precipitant.

3. (NH4)HO also precipitates Ca(HO)2, but the precipitate is soluble in excess.

4. Heated on charcoal with NaHCO3 in the reducing blow-pipe flaine, yields no metallic bead, but a brown incrustation of Cdo.

TABLE D. 72.-COPPER GROUP (II.). Separation of Mercury, Lead, Bismuth, Copper, and Cadmium (Sub-Group A).

To the filtrate from the Silver Group add an equal bulk of HCI, boil down nearly to dryness, dilute with

H2O, and pass H S through the hot solution. Filter.


HgS, PbS, Bi,S3, Cus, Cds, Sns, SnS2, Sb,S3, and As Sz.

Groups III., IV., and V.

Wash with hot H2O containing H, S, until free from Cl; digest residue with (NH4)2S, for about fifteen

minutes. Filter. RESIDUE.


HgS, PbS, Bi,S3, Cus and Cds.

Sub-Group B. (Sn, Sb, and As.)

(See Table E.)

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Wash with hot H,0 till no longer alkaline ; add a small quantity of boiling HNO3, pouring it on several

times. Filter.


Dissolve in aqua regia, boil down to expel acid,
and test with SnCly. White precipitate changing to
grey indicates Mercury. Confirm by reduction
test, or Bunsen's test for mercury (59).

Pb, Bi, Cu, cd.
Add H2SO4, and boil down. White precipitate in-
dicates Lead. Filter from PbSO4, and add (NH)HO
to filtrate. Filter.



Cu, cd.
A white precipitate. A blue solution indi-
Dissolve in HCl, evapo- cates Copper. Adopt
rate to a small bulk, and Method I. or II.
add to H2O. A white
precipitate indicates

Add to the blue solution KCN till colourless; pass
a few bubbles of H2S through the solution. Yellow
precipitate indicates Cadmium. (Excess of H2S
must be avoided, because traces of mercury may be

Add HCl till acid; pass HQS through ; filter ; wash
rapidly and thoroughly, and treat with hot dilute
H2SO4. Black residue indicates Copper. To fil-
trate, add H,S. Yellow precipitate indicates Cad-

73. SUB-GROUP B.-Sulphides soluble in (NH),S2 viz., those of Tin, Antimony, and Arsenic.

TIN, Sn, c.w. 18. Stannous Salts.

1. H S produces a dark brown precipitate of Sns, soluble in (NH4)2S, (yellow), but nearly insoluble in (NH4)2S (colourless). From its solution in (NH4)2S2 it is re-precipitated as SnS, (yellow) on adding HCl. SnS is also soluble in KHO, and, on the addition of acids, is re-precipitated as SnS (brown).

2. KHO produces a white precipitate of Sn (HO), soluble in excess of the reagent.

3. (NH)HO also produces a precipitate of Sn(HO) but not soluble in excess.

4. HgCl, produces at first a white precipitate of Hg,Cl2, and on boiling with excess of the reagent, a grey precipitate of Hg.

5. AuClz produces a purple precipitate (purple of Cassius) on addition of a little HNO3.

6. Zn produces a precipitate of metallic tin, in shining laminæ or as a spongy mass.

7. Mixed with NaHCO3 + KCN and heated on charcoal in the reducing blow-pipe flame, yields small globules of Sn and a white incrustation of SnO2.

Stannic Salts.—1. H2S produces a yellow precipitate of SnS2, soluble in (NH4)2S, in KHO, and in boiling concentrated HCl. It is with difficulty soluble int (NH)HO, and insoluble in (NH4)2CO3.

2. KHO or (NH)HO produces a white precipitate of SnO(HO),, soluble in an excess of the precipitant.

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