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extract; work the cotton in this at 160 deg. F. for three hours, then pass into a cold bath of 1 lb. copperas and 1/4 lb. chalk for half an hour, then into a bath of 3 lb. bichromate of potash for half an hour at 150 deg. F., then wash and dry. (7) PRODUCTION OF COLOUR DIRECT UPON COTTON FIBRES. By the action of nitrous acid upon the salts of the primary organic amines the so-called diazo compounds are formed. An example of this important process is that of nitrous acid on aniline hydrochloride shown in the following equation:-- C{6}H{5}NH{2} + HCl + HNO{2} 2H{2}O + C{6}H{5}N:NCl Hydrochloric acid Nitrous Water, Diazo-benzene aniline, acid, chloride. These diazo compounds are distinguished by their active properties, especially in combining with amines in acid solutions, or with phenols in alkaline solution to form the azo dyes, thus diazobenzene chloride will combine with naphthol to form naphthol-azo-benzene, thus:-- C{6}H{5}N:NCl + C{10}H{7}OH + NaOH = Diazo-benzene chloride, Naphthol, Caustic soda. C{10}H{6}OHN:NC{6}H{5} + NaCl + H{2}O Naphthol-azo-benzene, Salt, Water. These azo compounds are coloured, but are perfectly insoluble in water, alkalies, or acids; on the other hand the sulphonates of these bodies are easily soluble and form the numerous azo dyes now so largely made and used in wool and silk dyeing, but which on account of their being sulphonates cannot be used for cotton dyeing. Methods have been devised for producing the insoluble azo colours direct upon the fibres. They are also called naphthol colours from the use of beta-and alpha-naphthol in their production. Although these azo dyes, when produced on the fibre, do not possess the fastness of the alizarine dyes, yet, on account of their cheapness and relative great fastness to soap and the action of sunlight, they are better than many of the newer cotton dyes. By this method (first introduced in England by Holliday) colours of exceptional brightness and fastness can be obtained which were not obtainable with the dyes then known. Those which are obtained from phenols are of the first importance. _The Diazotisation of the Amido Bases._ With most bases this must be accomplished as cold as possible below 65 deg. F. At a higher temperature, and when allowed to stand, most diazo compounds decompose quickly with evolution of nitrogen, which decomposition results in the mixture l
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