Chromium alums sulphate

Hydrated chromium(III) sulphate exhibits different colours and different forms from which varying amounts of sulphate ion can be precipitated by barium chloride, due to the formation of sulphato-complexes. Chromium(III) sulphate can form alums. 

SYNS CHROME ALUM CHROME POTASH ALUM CHROMIC POTASSIUM SULFATE CHROMIC POTASSIUM SULPHATE CHROMIUM POTASSIUM SULFATE (1 1 2) CHROMIUM POTASSIUM SULPHATE CRYSTAL CHROME ALUM POTASSIUM CHROMIC SULPHATE POTASSIUM CHROMIUM ALUM POTASSIUM DISULPHATOCHROMATE(III) SULFURIC ACID, CHROMIUM (3+) POTASSIUM SALT (2 1 1)... 

If there is no available salt of constant composition, such as copper(II) sulphate or iron(III), aluminium or chromium alums, it is advisable to prepare first a stock solution of an approximate concentration, slightly higher than required and to determine the concentration by a gravimetric or volumetric method. After suitable calculations the solution is diluted with pure solvent to obtain a solution containing exactly, e.g., 1 mg/ml of the given element. In some cases, standard solutions are obtained by dissolving a precisely weighed amount of the element in its pure form. 

Subbing solution (5 X). Gelatin is dissolved in water at 65°C to make a 0.5% solution. This solution is cooled to room temperature and made 0.05% with respect to chrom alum ( = chromium potassium sulphate CrK(SO4)2-12H2O). Sterile water is used for further dilutions of the subbing solution. 

Chrome alum CrK(S04)2.12H2Q Chromium acid sulphate. Used In tanning and as a mordant in dying. 

Basicity chrome alum CCRIS 7532 Chrome alum Chrome potash alum Chromic potassium sulfate Chromic potassium sulphate Chromium potassium bis(sulphate) Chromium potassium sulfate (1 1 2) Chromium potassium sulfate (CrK(S04)2) Chromium potassium sulphate Chromium(lll) potassium sulfate Crystal Chrome Alum EINECS 233401-6 Potassium chromic sulfate Potassium chromic sulphate Potassium chromium alum Potassium chromium disulfate (KCr(S04)2) Potassium disulphatochromate (III) Sulfuric acid, chromium(3 ) potassium salt (2 1 1). Mordant for dyeing fabrics uniformly [dodecahydratej mp = 89° d = 1.83 soluble in 4 parts H2O. 

Til A 20-o iice bottle put 7 ounces of silicate of soda, till up the bottle with water, ami stir and shake well until a thorough IV lioniogeneons fluid is produced. This will take time and patience, but is absolutely necessary if the experiment is to be a success. Having done tliis, next put sand into the bottle or jar until it forms a layer at the bottom nearly half an inch thick. Tlie sand must be deposited quietly, and is best poured down a tube reaching to the bottom of the jar. Take a number of crystals of various substances such as alum, sulphates of iron, copper, chromium, etc., and with a glass rod finnly embed them in tlie sand, about half covering them but no more. The bottle or jar must then be set aside and left absolutely undisturbed. In course of time the crystals will spout rut in filaments, etc., of varying colours. 

Chromium alum Cr2(S04)3K2S04-24H20 (double sulphate of potassium and chromium)... 

The dichromate ion oxidises iron(II) to iron(III), sulphite to sulphate ion, iodide ion to iodine and arsenic(III) to arsenic(V) (arsenate). Reduction of dichromate by sulphite can be used to prepare chrome alum, since, if sulphur dioxide is passed into potassium dichromate acidified with sulphuric acid, potassium and chromium(III) ions formed are in the correct ratio to form the alum, which appears on crystallisation ... 

The halogenates of chromium, uranium, and manganese.—The double decomposition of chrome alum and barium chlorate, or a soln. of chromic sulphate and potassium chlorate, furnishes a violet liquid containing chromium chlorate,134 which becomes green at 65°. Even at ordinary temp, the soln. smells of chlorine at 100°, chlorine gas is given off and the liquid becomes reddish-yellow—it contains chromic... 

The preparation of potassium dichromate (Preparation 61) illustrated how chromic oxide, Cr203, can be oxidized to a chromate in which chromium exists as Cr03. For the preparation of chromic alum, it might seem as if chromic oxide or the natural chromite should yield chromic sulphate directly on treatment with sulphuric acid. This is impossible, however, because both of these substances are very resistant to the action of acids. Practically, they yield only to the action of alkaline oxidizing agents, which convert them into a chromate. Therefore potassium, or sodium, dichromates are always the products made directly from the mineral, and these serve as the materials from which other compounds of chromium are prepared. To make chromic alum from potassium dichromate it is necessary to reduce the chromium to the state of oxidation in which it originally existed in the mineral, and to add sufficient sulphuric acid to form the sulphates of potassium and... 

Cobaltic sulphate, like the sulphates of rhodium and iridium, unites with the sulphates of the alkali metals to yield a series of well-defined, crystalline salts known as alums. These are isomorphous with those of iron, manganese, chromium, and aluminium, and form an interesting link between these metals and the central vertical column in Group VIII of the Periodic Table, of which column cobalt is the first member. 

Chromium in its Compounds is sometimes metallic and sometimes non-metallic toward the other components. Thus, in chromium trioxide, CrOg, the anhydride of the hypothetical chromic acid, H2Cr04, chromium acts as a non-metal, just like sulphur in sulphuric acid hence in chromates the chromium is acidic, or non-metallic, in its chemical relations with the other elements. In chromic compounds, however, chromium acts as a metal. Thus chromium hydroxide, Cr(OH)3, is analogous to aluminium hydroxide chrome alum is potassium chromium sulphate, and is analogous to aluminium alum. The two classes pass into each other by appropriate operations,... 

The chromous salts, derived from the oxide CrO, arc analogous to the salts of divalent vanadium, manganese, and iron. This is seen in the isomorphism of the sulphates of the type R" SOj-THgO. The stability of such salts increases in the order of the atomic number of the metal. The chief basic oxide of chromium is the sesquioxidc CraO, which is closely allied to ferric oxide, and, like the latter, resembles aluminium oxide. The hydroxide, Cr(OH)3, with bases yields chromites analogous to, but less stable than, the aluminates. Chromic sulphate enters into the formation of alums. The chromic salts are very stable, but in the trivaJent condition the metal shows a marked tendency to form complex ions, both anions and cations thus it resembles iron in producing complex cyanides, whilst it also yields compounds similar to the cobaltamines. 

The sesquioxide, Cr Oa, containing trivalent chromium, is an amphoteric oxide. It yields chromic salts, such as chromic chloride, CrCla, and sulphate, Cr2(S04)a, which are very stable and show great similarity to the ferric salts and to salts of aluminium as, for example, in the formation of alums. Since, however, chromic oxide functions as a weaker base than chromous oxide, the latter having a lower oxygen content, the chromic salts are more liable to hydrolysis than the chromous salts. This is well marked in the case of the chlorides. Again, in spite of the stability of chromic salts, only a slight tendency to form simple Cr " ions is exhibited, whilst complex ions are formed much more readily, not only complex anions, as in the case of iron and aluminium, but also complex cations, as in the extensive chromammine series. In this respect chromium resembles cobalt and platinum. 

But the admirable researches of Gay-Lussac and of Mitscherlich have established the fact, that in many instances, different compounds assume the same form. Thus, the following substances, and many others, take the form of the cube, tetrahedron, or regular octohedron, which are geometrically connected. Chloride of sodium (sea-salt), chloride of potassium, sal ammoniac bromide of potassium iodide of potassium sulphuret of lead fluoride of calcium bisnlphuret of iron arseniuret of cobalt sulphate of alumina and potash (alum) ammonia alum chrome alum, iron alum sesqnioxide of iron, sesquioxide of aluminum, sesquioxide of chromium. In like manner, other crystalline forms are found to be common to many different compounds, although none occurs so frequently as the cube and its congeners. 

Cowper-Coles found that a soln. of 100 parts of chrome-alum in 100 parts of water with 12 parts of barium sulphate does not yield a deposit of chromium metal on electrolysis. E. Placet found that when a soln. of chrome-alum and an alkali sulphate acidified with sulphuric acid, is electrolyzed, chromium is deposited at the cathode as a hard, bluish-white, lustrous metal, which, under certain conditions, crystallizes in groups resembling the branching of firs. Other metals and alloys— bronze, copper, iron, brass, etc.—may be plated with chromium, and a surface can be obtained to resemble oxidized silver. E. Placet and J. Bonnet have a number of patents on this subject. 

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