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    • 2. 发明授权
    • Separation of cobalt and nickel by oxidative precipitation with
peroxymonosulfuric acid
    • 用过氧单硫酸氧化沉淀分离钴和镍
    • US4394357A
    • 1983-07-19
    • US321575
    • 1981-11-16
    • Diana M. MounseyDavid B. Mobbs
    • Diana M. MounseyDavid B. Mobbs
    • B01D20060101C01G20060101C01G51/00C01G51/04C01G53/00C01G53/10C07F15/04C22B20060101C22C19/00C25C1/20
    • C22B23/0484
    • The invention relates to the preferential precipitation of cobalt from aqueous acidic sulphate solutions of nickel and cobalt.The separation is carried out by introducing at least a stoichiometric amount of Caro's Acid containing no more than a small amount of hydrogen peroxide into the nickel/cobalt solution progressively over a period of at least an hour, while maintaining the solution of a pH from 3.1 or 3.5 up to 4.7 by addition of an alkali metal hydroxide carbonate or bicarbonate, or at 4.3 to 4.7 with the corresponding ammonium compound, and, thereafter separating the precipitate from the aqueous cobalt depleted solution.In preferred features, the Caro's Acid solution used contains hydrogen peroxide in a mole ratio to peroxomonosulphuric acid of not more than 1:10; the Caro's Acid solution is introduced continuously or in increments of less than 1% of the total over a period of at least an hour; the Caro's Acid is produced by reaction between 93-98% sulphuric acid and 65-72% aqueous hydrogen peroxide in a mole ratio of 2.7:1 to 3.5:1; the Caro's Acid solution is diluted before use; and particular amounts of Caro's Acid are used depending upon the nature of the nickel/cobalt solution, the mode of treatment, and the nature of the neutralizing agent. Further separation can be effected by subsequent water and particularly not acid washing of the precipitate.
    • 本发明涉及钴从镍和钴的酸性硫酸盐水溶液中优先沉淀。 通过在至少1小时的时间内将至少含有不超过少量过氧化氢的化学计量量的Caro酸向镍/钴溶液中逐渐引入,同时保持pH为3.1的溶液来进行分离 或通过加入碱金属氢氧化物碳酸盐或碳酸氢盐,或在4.3至4.7℃下加入相应的铵化合物,然后从含钴贫化溶液中分离出沉淀物,3.5至4.7。 在优选的特征中,所用Caro's酸溶液含有与过氧二硫酸的摩尔比不大于1:10的过氧化氢; Caro酸溶液在至少一小时内持续或以小于总量的1%的增量引入; 卡罗酸是通过93-98%硫酸和65-72%过氧化氢水溶液之间的摩尔比为2.7:1至3.5:1的反应产生的; 使用前将Caro's Acid溶液稀释; 并且根据镍/钴溶液的性质,处理方式和中和剂的性质,使用特定量的Caro酸。 进一步的分离可以通过随后的水进行,特别是不是酸洗该沉淀物。
    • 4. 发明授权
    • Process for waste treatment
    • 废物处理工艺
    • US4729835A
    • 1988-03-08
    • US910969
    • 1986-09-24
    • Alastair McNeillieDavid B. Mobbs
    • Alastair McNeillieDavid B. Mobbs
    • C02F1/72
    • C02F1/725C02F1/722Y10S210/916
    • Organic sulphides are extremely malodorous compounds that are found in gaseous or aqueous effluents from many industries such as paper and pulp manufacture, hydrocarbon refinering, tanneries, and in the synthesis of organic sulphur compounds. Their removal is necessary before such effluents can be discharged into the environment.In the present invention their removal is effected using hydrogen peroxide at a pH controlled to pH 8.5 to 11.5 and in the presence of a catalytic amount of a soluble tungstate. Such a process is especially applicable to the removal of dialkyl disulphides, which are regarded as being especially difficult to remove oxidatively. In especially preferred conditions, the pH is about pH 11 and about 3-4 moles H.sub.2 O.sub.2 is used per mole equivalent of sulphur, in the presence of at least 20 ppm sodium tungstate (as W).
    • 有机硫化物是在许多行业的气态或水性流出物中发现的非常恶臭的化合物,例如纸和纸浆制造,烃精炼,制革厂和有机硫化合物的合成。 在将这些废水排放到环境中之前,必须拆除它们。 在本发明中,使用过氧化氢在pH值控制在pH 8.5至11.5,并在催化量的可溶性钨酸盐存在下进行除去。 这种方法特别适用于去除被认为特别难以氧化去除的二烷基二硫化物。 在特别优选的条件下,在至少20ppm钨酸钠(如W)存在下,pH为约11,并且每摩尔当量硫使用约3-4摩尔H 2 O 2。