首页> 外国专利> SEPARATION OF COBALT FROM NICKEL AND COBALT BEARING AMMONIACAL SOLUTIONS

SEPARATION OF COBALT FROM NICKEL AND COBALT BEARING AMMONIACAL SOLUTIONS

机译:从镍和含钴氨溶液中分离钴

摘要

1344549 Cobalt and nickel separation SHERRITT GORDON MINES Ltd 14 Feb 1972 [5 March 1971] 6837/72 Heading C1A Nickel and cobalt bearing material is leached in one or more stages under oxidizing conditions with an ammonium salt leach solution, the solution from the leach operation being treated in at least two cobalt removal stages with a sulphidizing agent to form a mixed Nickelcobalt sulphide precipitate, the agent in one stage being sufficient to produce a Ni-Co ratio in the treated solution of 500 : 1 or over, the agent in another stage being sufficient to cause the precipitate formed therein to have a Ni-Co ratio of 2 : 1 or lower; the precipitate is removed from each stage and at least a portion is recycled to the solution from which it was removed, the un-recycled portion of the precipitate from the other stage is removed as mixed Ni-Co sulphide product and any unrecycled precipitate formed in said one stage is added to a further stage, at least a portion of solution from the other stage is recycled to the leach operation and the solution from said one stage is recovered as product liquor for subsequent treatment to yield nickel. Where three cobalt removal stages are used, 1, 2 and 3 in conjunction with two leaching stages, A and B, solution from A is treated in 2, the precipitate in 2 being separated and a portion being recycled to 2, the remainder with solution from B being passed to 3, solution from 2 being passed to 1 and the un-recycled portion of the precipitate from 1 is passed to 2. The sulphidizing agents may be H 2 S, (NH 4 ) 2 S, Na 2 S and NaHS. The product liquor may be maintained at 65-70‹ C. for a time sufficient to precipitate contained sulphides and manganese which are separated. The Ni-Co sulphide product may be washed with (NH 4 ) 2 CO 3 , the wash solution, after washing, being recycled to the leaching operation.
机译:1344549钴和镍的分离SHERRITT GORDON MINES Ltd 1972年2月14日[1971年3月5日] 6837/72品目C1A在氧化条件下,用铵盐浸出液分第一步或多次浸出含镍和钴的材料,该溶液来自浸出操作在至少两个脱钴步骤中用硫化剂处理以形成混合的镍钴钴沉淀物,该试剂在一个步骤中足以在处理后的溶液中产生500:1或更高的Ni-Co比,在另一阶段中足以产生Ni-Co比该阶段足以使其中形成的沉淀物的Ni-Co比为2∶1或更低。从每个阶段除去沉淀物,并将至少一部分再循环至从中除去沉淀物的溶液,将另一阶段沉淀物中未回收的部分作为混合的Ni-Co硫化物产物除去,并在其中形成任何未回收的沉淀物将所述一个阶段添加到另一阶段,将来自另一阶段的至少一部分溶液再循环至浸提操作,并将来自所述一个阶段的溶液作为产物液回收,用于后续处理以产生镍。在使用三个脱钴步骤,1、2和3以及两个浸出步骤A和B的情况下,将A中的溶液在2中进行处理,将2中的沉淀物分离出来,并将一部分再循环到2中,其余的则与溶液一起处理从B转移到3,将溶液从2转移到1,并将沉淀的未再循环部分从1转移到2。硫化剂可以是H 2 S,(NH 4)2 S,Na 2 S和NaHS。产物液可以在65-70℃下保持足以沉淀分离出的硫化物和锰的时间。 Ni-Co硫化物产物可以用(NH 4)2 CO 3洗涤,洗涤后的洗涤溶液再循环到浸出操作中。

著录项

  • 公开/公告号FR2128549B1

    专利类型

  • 公开/公告日1976-06-11

    原文格式PDF

  • 申请/专利权人 SHERRITT GORDON MINES;

    申请/专利号FR19720007289

  • 发明设计人

    申请日1972-03-02

  • 分类号C22B23/00;C01G51/00;C01G53/00;

  • 国家 FR

  • 入库时间 2022-08-23 01:55:05

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