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disulphide

disulphide Sentence Examples

  • The disulphide, IrS2, is formed when powdered iridium is heated with sulphur and an alkaline carbonate.

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  • Molybdenum disulphide, MoS 2, is found as the mineral molybdenite, and may be prepared by heating the trioxide with sulphur or sulphuretted hydrogen.

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  • It is a brown powder which on heating in air loses sulphur and leaves a residue of the disulphide.

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  • If excess of a mineral acid be added to a solution of an alkaline thiogermanate a white precipitate of germanium disulphide, GeS2, is obtained.

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  • By heating the disulphide in a current of hydrogen, germanious sulphide, GeS, is formed.

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  • The germanium salts are most readily recognized by the white precipitate of the disulphide, formed in acid solutions, on passing sulphuretted hydrogen.

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  • This salt, on standing, decomposes into barium dithionate, BaS206, and diethyl disulphide, (C2H5)2S2, which points to the presence of the SH group in the molecule.

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  • Passing over the discovery of carbon disulphide by W.

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  • Normal values of K were given by nitrogen peroxide, N204, sulphur chloride, S 2 C1 21 silicon tetrachloride, SiC1 4, phosphorus chloride, PC1 3, phosphoryl chloride, POC1 31 nickel carbonyl, Ni(CO) 4, carbon disulphide, benzene, pyridine, ether, methyl propyl ketone; association characterized many hydroxylic compounds: for ethyl alcohol the factor of association was 2.74-2.43, for n-propyl alcohol 2.86-2.72, acetic acid 3.62 -2.77, acetone 1 .

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  • If the gas be mixed with the vapour of carbon disulphide, the mixture burns with a vivid lavender-coloured flame Nitric oxide is soluble in solutions of ferrous salts, a dark brown solution being formed, which is readily decomposed by heat, with evolution of nitric oxide.

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  • cystin (stone-cystin), or a-thio-/3-aminoglyceric acid " disulphide," (NH 2 � CH 2 � CH: S.

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  • Either they are placed in a leaden cupboard into which the vapour is introduced, or they are dipped for a few seconds in a mixture of one part of chloride of sulphur and forty parts of carbon disulphide or purified light petroleum.

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  • The light oil fraction of the coal-tar distillate, which comes over below 140° and consists principally of benzene, toluene and the xylenes, yields on fractionation (i) various volatile impurities such as carbon disulphide, (2) the benzene fraction boiling at about 80° C., (3) the toluene fraction boiling at too°, (4) the xylene fraction boiling at 140°.

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  • Its specific gravity is o 899 at o° C. It is very slightly soluble in water, more soluble in alcohol, and completely miscible with ether, acetic acid and carbon disulphide.

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  • Aqueous alcohol becomes turbid when mixed with benzene, carbon disulphide or paraffin oil; when added to a solution of barium oxide in absolute alcohol, a white precipitate of barium hydroxide is formed.

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  • Bismuth combines directly with sulphur to form a disulphide, B12S2, and a trisulphide, B12S3, the latter compound being formed when the sulphur is in excess.

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  • A hydrated disulphide, B12S2.2H20, is obtained by passing sulphuretted hydrogen into a solution of bismuth nitrate and stannous chloride.

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  • Bismuth disulphide is a grey metallic substance, which is decomposed by hydrochloric acid with the separation of metallic bismuth and the formation of bismuth trichloride.

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  • The solubility of the gas in various liquids, as given by different observers, is zoo Volumes of Brine Water Alcohol Paraffin Carbon disulphide Fusel oil Benzene Chloroform Acetic acid Acetone It will be seen from this table that where it is desired to collect and keep acetylene over a liquid, brine, i.e.

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  • Under the same conditions it becomes incandescent in the vapour of sulphur, yielding calcium sulphide and carbon disulphide; the vapour of phosphorus will also unite with it at a red heat.

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  • Osmium disulphide, OsS2, is obtained as a dark brown precipitate, insoluble in water, by passing sulphuretted hydrogen into a solution of an osmichloride.

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  • MARCASITE, a mineral with the same chemical composition as pyrites, being iron disulphide FeS2, but crystallizing in the orthorhombic instead of in the cubic system.

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  • Marcasite is thus the less stable of the two modifications of iron disulphide.

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  • Heated in chlorine or with bromine, it yields carbon and calcium chloride or bromide; at a dull red heat it burns in oxygen, forming calcium carbonate, and it becomes incandescent in sulphur vapour at 500°, forming calcium sulphide and carbon disulphide.

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  • The disulphide, CaS2, and pentasulphide, CaS 5, are formed when milk of lime is boiled with flowers of sulphur.

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  • Aluminium sulphide, Al2S3, results from the direct union of the metal with sulphur, or when carbon disulphide vapour is passed over strongly heated alumina.

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  • PYRITES, a term applied to iron disulphide when crystallized in the cubic system, but used also in a general sense to designate a group of metallic sulphides of which this mineral is the most characteristic example.

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  • In some cases the two forms of iron disulphide occur in intimate association and are difficult to distinguish.

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  • When heated in a current of hydrogen it is transformed into the colourless disulphide, whilst if the heating be carried out in a current of nitrogen it yields the trisulphide, Rb 2 S 3 H 2 0.

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  • Tungsten disulphide, W52, is obtained as soft black acicular crystals by the action of sulphur, sulphuretted hydrogen or carbon bisulphide on tungsten.

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  • The carbon disulphide and salicylic aldehyde products have also been used as means of distinction, as has also the formation of the stilbazonium bases obtained by condensing ortho-semidines with benzil (0.

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  • Phosphorus trichloride or phosphorous chloride, PC13, discovered by Gay-Lussac and Thenard in 1808, is obtained by passing a slow current of chlorine over heated red phosphorus or through a solution of ordinary phosphorus in carbon disulphide (purifying in the latter case by fractional distillation).

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  • Phosphorus tribromide, PBr 3, prepared by mixing solutions of its elements in carbon disulphide and distilling, is a transparent, mobile liquid, boiling at 173° and resembling the trichloride chemically.

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  • Boulough (Comptes rendus, 1905, 141, p. 256), who acted with dry iodine on phosphorus dissolved in carbon disulphide; with alkalis it gives P 4 (OH).

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  • The product is extracted with carbon disulphide and the residue distilled in carbon dioxide.

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  • The second, P4S7, is obtained by heating a mixture of red phosphorus and sulphur in the proportions given by P4S7+5% P4S3, and crystallizing from carbon disulphide in which P 4 S 3 is readily soluble.

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  • Thiel (Ber., 1905, 3 8, p. 2719 1910, 43, p. 1223), who heated sulphur with phosphorus in carbon disulphide solution with a trace of iodine to 120 0 -130 0.

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  • more or less pure disulphide of iron which occurs in large quantities in many countries.

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  • At this point in the manufacturing process the gas has already undergone some important changes in its composition, but there yet remain impurities which must be removed, these being ammonia, sulphuretted hydrogen, carbon disulphide and carbon dioxide.

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  • In this wet purifying apparatus the gas is almost wholly freed from ammonia and from part of the sulphuretted hydrogen, whilst carbon dioxide and carbon disulphide are also partially extracted.

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  • When the gas had to be purified from carbon disulphide as well as from sulphuretted hydrogen, slaked lime was employed for the removal of carbon dioxide and the greater quantity of the sulphur compounds, whilst a catch box or purifier of oxide of iron served to remove the last traces of sulphuretted hydrogen.

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  • This operation was necessitated by the fact that carbon dioxide has the power of breaking up the sulphur compounds formed by the lime, so that until all carbon dioxide is absorbed with the formation of calcium carbonate, the withdrawal of sulphuretted hydrogen cannot proceed, whilst since it is calcium sulphide formed by the absorption of sulphuretted hydrogen by the slaked lime that absorbs the vapour of carbon disulphide, purification from the latter can only be accomplished after the necessary calcium sulphide has been formed.

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  • The foul gas leaving the scrubbers contains, as a general average, 30 grains of sulphuretted hydrogen, 40 grains of carbon disulphide and zoo grains of carbon dioxide per Ioo cub.

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  • On entering the first purifier, which contains calcium thiocarbonate and other combinations of calcium and sulphur in small quantity, the sulphuretted hydrogen and disulphide vapour have practically no action upon the material, but the carbon dioxide immediately attacks the calcium thiocarbonate, forming calcium carbonate with the production of carbon disulphide vapour, which is carried over with the gas into the second box.

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  • In the connexion between the first and the second box the gas is found to contain 500 grains of sulphuretted hydrogen and 80 grains of carbon disulphide per Ioo cub.

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  • In the second box the formation of calcium thiocarbonate takes place by the action of carbon disulphide upon the calcium sulphide with the liberation of sulphuretted hydrogen, which is carried over to the third purifier.

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  • The gas in the connecting pipe between the second and third purifier will be found to contain 400 grains of sulphuretted hydrogen and 20 grains of carbon disulphide.

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  • The contents of the third box, being mostly composed of slaked lime, take up sulphuretted hydrogen forming calcium sulphide, and practically remove the remaining impurities, the outlet gas showing 20 grains of sulphuretted hydrogen and 8 grains of carbon disulphide per Ioo cub.

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  • It will be noticed that in the earlier stages the quantity of sulphur impurities is actually increased between the purifiers - in fact, the greater amount of sulphiding procures the ready removal of the carbon disulphide, - but it is the carbon dioxide in the gas that is the disturbing element, inasmuch as it decomposes the combinations of sulphur and calcium; consequently it is a paramount object in this system to prevent this latter impurity finding its way through the first box of the series.

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  • Iron disulphide, FeS2, constitutes the minerals pyrite and marcasite; copper pyrites is (Cu, Fe)S2.

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  • Sulphuretted hydrogen is passed through the liquid until it is thoroughly saturated, the excess of sulphuretted hydrogen is expelled from the solution by a brisk stream of carbon dioxide, and the precipitate is filtered on a Gooch crucible and washed with water containing a little sulphuretted hydrogen and dried at 100° C.; it is then well washed with small quantities of pure carbon disulphide to remove any free sulphur, again dried and weighed.

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  • Aniline combines directly with alkyl iodides to form secondary and tertiary amines; boiled with carbon disulphide it gives sulphocarbanilide (diphenyl thio-urea), CS(NHC 6 H 5) 2, which may be decomposed into phenyl mustard-oil, C 6 H 5 CNS, and triphenyl guanidine, C 6 H 5 N: C(NHC6H5)2.

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  • The disulphide, IrS2, is formed when powdered iridium is heated with sulphur and an alkaline carbonate.

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  • Molybdenum disulphide, MoS 2, is found as the mineral molybdenite, and may be prepared by heating the trioxide with sulphur or sulphuretted hydrogen.

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  • It is a brown powder which on heating in air loses sulphur and leaves a residue of the disulphide.

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  • If excess of a mineral acid be added to a solution of an alkaline thiogermanate a white precipitate of germanium disulphide, GeS2, is obtained.

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  • By heating the disulphide in a current of hydrogen, germanious sulphide, GeS, is formed.

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  • The germanium salts are most readily recognized by the white precipitate of the disulphide, formed in acid solutions, on passing sulphuretted hydrogen.

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  • This salt, on standing, decomposes into barium dithionate, BaS206, and diethyl disulphide, (C2H5)2S2, which points to the presence of the SH group in the molecule.

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  • Passing over the discovery of carbon disulphide by W.

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  • Normal values of K were given by nitrogen peroxide, N204, sulphur chloride, S 2 C1 21 silicon tetrachloride, SiC1 4, phosphorus chloride, PC1 3, phosphoryl chloride, POC1 31 nickel carbonyl, Ni(CO) 4, carbon disulphide, benzene, pyridine, ether, methyl propyl ketone; association characterized many hydroxylic compounds: for ethyl alcohol the factor of association was 2.74-2.43, for n-propyl alcohol 2.86-2.72, acetic acid 3.62 -2.77, acetone 1 .

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  • If the gas be mixed with the vapour of carbon disulphide, the mixture burns with a vivid lavender-coloured flame Nitric oxide is soluble in solutions of ferrous salts, a dark brown solution being formed, which is readily decomposed by heat, with evolution of nitric oxide.

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  • cystin (protein-cystin) or a-amino-,-thioglyceric acid " disulphide," (S.

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  • cystin (stone-cystin), or a-thio-/3-aminoglyceric acid " disulphide," (NH 2 � CH 2 � CH: S.

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  • Either they are placed in a leaden cupboard into which the vapour is introduced, or they are dipped for a few seconds in a mixture of one part of chloride of sulphur and forty parts of carbon disulphide or purified light petroleum.

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  • If cotton or linen is used, it is usual to incorporate sulphur with the paste, and to effect vulcanization by steam heat; but, when silk or wool is employed, no sulphur is added to the paste, the dried coating of rubber being merely brought into momentary contact with the mixture of chloride of sulphur and carbon disulphide already mentioned.

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  • The light oil fraction of the coal-tar distillate, which comes over below 140° and consists principally of benzene, toluene and the xylenes, yields on fractionation (i) various volatile impurities such as carbon disulphide, (2) the benzene fraction boiling at about 80° C., (3) the toluene fraction boiling at too°, (4) the xylene fraction boiling at 140°.

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  • Its specific gravity is o 899 at o° C. It is very slightly soluble in water, more soluble in alcohol, and completely miscible with ether, acetic acid and carbon disulphide.

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  • It may be obtained by distilling benzyl sulphide !or disulphide, by the action of sodium on benzaldehyde or benzal chloride, by distilling fumaric and cinnamic phenyl esters: C6H50.OC CH:CH CO.OC6H5 - >C02+C6H5.CH:CH CO.006H5 - >2C02 -{-C 6 H 5 CH: CH C 6 H 5 (Ber., 18, p.1945), and fromchlorasymmetrical diphenylethane derivatives which undergo a rearrangement when heated (Ber., 7.

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  • Aqueous alcohol becomes turbid when mixed with benzene, carbon disulphide or paraffin oil; when added to a solution of barium oxide in absolute alcohol, a white precipitate of barium hydroxide is formed.

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  • Bismuth combines directly with sulphur to form a disulphide, B12S2, and a trisulphide, B12S3, the latter compound being formed when the sulphur is in excess.

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  • A hydrated disulphide, B12S2.2H20, is obtained by passing sulphuretted hydrogen into a solution of bismuth nitrate and stannous chloride.

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  • Bismuth disulphide is a grey metallic substance, which is decomposed by hydrochloric acid with the separation of metallic bismuth and the formation of bismuth trichloride.

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  • The solubility of the gas in various liquids, as given by different observers, is zoo Volumes of Brine Water Alcohol Paraffin Carbon disulphide Fusel oil Benzene Chloroform Acetic acid Acetone It will be seen from this table that where it is desired to collect and keep acetylene over a liquid, brine, i.e.

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  • Under the same conditions it becomes incandescent in the vapour of sulphur, yielding calcium sulphide and carbon disulphide; the vapour of phosphorus will also unite with it at a red heat.

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  • Osmium disulphide, OsS2, is obtained as a dark brown precipitate, insoluble in water, by passing sulphuretted hydrogen into a solution of an osmichloride.

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  • MARCASITE, a mineral with the same chemical composition as pyrites, being iron disulphide FeS2, but crystallizing in the orthorhombic instead of in the cubic system.

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  • Marcasite is thus the less stable of the two modifications of iron disulphide.

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  • Heated in chlorine or with bromine, it yields carbon and calcium chloride or bromide; at a dull red heat it burns in oxygen, forming calcium carbonate, and it becomes incandescent in sulphur vapour at 500°, forming calcium sulphide and carbon disulphide.

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  • The disulphide, CaS2, and pentasulphide, CaS 5, are formed when milk of lime is boiled with flowers of sulphur.

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  • Aluminium sulphide, Al2S3, results from the direct union of the metal with sulphur, or when carbon disulphide vapour is passed over strongly heated alumina.

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  • PYRITES, a term applied to iron disulphide when crystallized in the cubic system, but used also in a general sense to designate a group of metallic sulphides of which this mineral is the most characteristic example.

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  • In some cases the two forms of iron disulphide occur in intimate association and are difficult to distinguish.

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  • Manganese Disulphide, MnS2, found native as hauerite, is formed as a red coloured powder by heating manganous sulphate with potassium polysulphide in a sealed tube at 160°-170° C. (H.

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  • When heated in a current of hydrogen it is transformed into the colourless disulphide, whilst if the heating be carried out in a current of nitrogen it yields the trisulphide, Rb 2 S 3 H 2 0.

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  • Tungsten disulphide, W52, is obtained as soft black acicular crystals by the action of sulphur, sulphuretted hydrogen or carbon bisulphide on tungsten.

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  • The carbon disulphide and salicylic aldehyde products have also been used as means of distinction, as has also the formation of the stilbazonium bases obtained by condensing ortho-semidines with benzil (0.

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  • Phosphorus trichloride or phosphorous chloride, PC13, discovered by Gay-Lussac and Thenard in 1808, is obtained by passing a slow current of chlorine over heated red phosphorus or through a solution of ordinary phosphorus in carbon disulphide (purifying in the latter case by fractional distillation).

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  • Phosphorus tribromide, PBr 3, prepared by mixing solutions of its elements in carbon disulphide and distilling, is a transparent, mobile liquid, boiling at 173° and resembling the trichloride chemically.

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  • Boulough (Comptes rendus, 1905, 141, p. 256), who acted with dry iodine on phosphorus dissolved in carbon disulphide; with alkalis it gives P 4 (OH).

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  • The product is extracted with carbon disulphide and the residue distilled in carbon dioxide.

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  • The second, P4S7, is obtained by heating a mixture of red phosphorus and sulphur in the proportions given by P4S7+5% P4S3, and crystallizing from carbon disulphide in which P 4 S 3 is readily soluble.

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  • Thiel (Ber., 1905, 3 8, p. 2719 1910, 43, p. 1223), who heated sulphur with phosphorus in carbon disulphide solution with a trace of iodine to 120 0 -130 0.

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  • more or less pure disulphide of iron which occurs in large quantities in many countries.

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  • At this point in the manufacturing process the gas has already undergone some important changes in its composition, but there yet remain impurities which must be removed, these being ammonia, sulphuretted hydrogen, carbon disulphide and carbon dioxide.

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  • In this wet purifying apparatus the gas is almost wholly freed from ammonia and from part of the sulphuretted hydrogen, whilst carbon dioxide and carbon disulphide are also partially extracted.

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  • When the gas had to be purified from carbon disulphide as well as from sulphuretted hydrogen, slaked lime was employed for the removal of carbon dioxide and the greater quantity of the sulphur compounds, whilst a catch box or purifier of oxide of iron served to remove the last traces of sulphuretted hydrogen.

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  • This operation was necessitated by the fact that carbon dioxide has the power of breaking up the sulphur compounds formed by the lime, so that until all carbon dioxide is absorbed with the formation of calcium carbonate, the withdrawal of sulphuretted hydrogen cannot proceed, whilst since it is calcium sulphide formed by the absorption of sulphuretted hydrogen by the slaked lime that absorbs the vapour of carbon disulphide, purification from the latter can only be accomplished after the necessary calcium sulphide has been formed.

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  • The foul gas leaving the scrubbers contains, as a general average, 30 grains of sulphuretted hydrogen, 40 grains of carbon disulphide and zoo grains of carbon dioxide per Ioo cub.

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  • On entering the first purifier, which contains calcium thiocarbonate and other combinations of calcium and sulphur in small quantity, the sulphuretted hydrogen and disulphide vapour have practically no action upon the material, but the carbon dioxide immediately attacks the calcium thiocarbonate, forming calcium carbonate with the production of carbon disulphide vapour, which is carried over with the gas into the second box.

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  • In the connexion between the first and the second box the gas is found to contain 500 grains of sulphuretted hydrogen and 80 grains of carbon disulphide per Ioo cub.

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  • In the second box the formation of calcium thiocarbonate takes place by the action of carbon disulphide upon the calcium sulphide with the liberation of sulphuretted hydrogen, which is carried over to the third purifier.

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  • The gas in the connecting pipe between the second and third purifier will be found to contain 400 grains of sulphuretted hydrogen and 20 grains of carbon disulphide.

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  • The contents of the third box, being mostly composed of slaked lime, take up sulphuretted hydrogen forming calcium sulphide, and practically remove the remaining impurities, the outlet gas showing 20 grains of sulphuretted hydrogen and 8 grains of carbon disulphide per Ioo cub.

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  • It will be noticed that in the earlier stages the quantity of sulphur impurities is actually increased between the purifiers - in fact, the greater amount of sulphiding procures the ready removal of the carbon disulphide, - but it is the carbon dioxide in the gas that is the disturbing element, inasmuch as it decomposes the combinations of sulphur and calcium; consequently it is a paramount object in this system to prevent this latter impurity finding its way through the first box of the series.

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  • Iron disulphide, FeS2, constitutes the minerals pyrite and marcasite; copper pyrites is (Cu, Fe)S2.

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  • Sulphuretted hydrogen is passed through the liquid until it is thoroughly saturated, the excess of sulphuretted hydrogen is expelled from the solution by a brisk stream of carbon dioxide, and the precipitate is filtered on a Gooch crucible and washed with water containing a little sulphuretted hydrogen and dried at 100° C.; it is then well washed with small quantities of pure carbon disulphide to remove any free sulphur, again dried and weighed.

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  • Aniline combines directly with alkyl iodides to form secondary and tertiary amines; boiled with carbon disulphide it gives sulphocarbanilide (diphenyl thio-urea), CS(NHC 6 H 5) 2, which may be decomposed into phenyl mustard-oil, C 6 H 5 CNS, and triphenyl guanidine, C 6 H 5 N: C(NHC6H5)2.

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