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A process for preparing high-purity uranium values from uranium ore concentrates

机译:从铀精矿中制备高纯度铀的方法

摘要

A solution containing uranium substantially free from other metals is obtained by preparing an aqueous solution of a uranium ore concentrate, having a pH from 0.1-3.0, contacting the solution with a solution of a dialkyl phosphate in an organic water-immiscible solvent and separating the resultant uranium-bearing organic phase from the aqueous phase. The initial solution is prepared by the use of an oxidising agent with a mineral acid, e.g. sodium perchlorate with hydrochloric acid, or with an oxidising acid such as nitric acid; hydrogen peroxide and manganese dioxide are also referred to as oxidising agents, and sulphuric acid is mentioned. The aqueous solution is then intimately mixed with the organic phase in an extractor. The preferred dialkyl phosphate is di-(2-ethylhexyl)phosphoric acid and suitable solvents are kerosene, naphtha, heptane or other water-immiscible aliphatic hydrocarbon. The phases are separated and the uranium-containing organic phase may be scrubbed with a small amount of dilute hydrochloric acid and stripped e.g. with sodium or ammonium hydroxide or carbonate solutions or concentrated hydrochloric acid. If hydrochloric acid is used, the solution may be evaporated to dryness and the resultant uranyl chloride calcined to U3O8, or evaporated to eliminate excess hydrochloric acid (which can be recycled), diluted with water and the uranium precipitated with ammonia as ammonium diuranate which can be calcined to oxide.
机译:通过制备具有0.1-3.0的pH值的铀矿精矿的水溶液,使该溶液与磷酸二烷基酯在不与水混溶的有机溶剂中接触并将其分离,从而获得基本上不含其他金属的铀溶液。由水相得到的含铀有机相。初始溶液是通过使用氧化剂与无机酸,例如无机酸来制备的。高氯酸钠与盐酸,或与氧化性酸,如硝酸;过氧化氢和二氧化锰也被称为氧化剂,并且提及硫酸。然后在萃取器中将水溶液与有机相充分混合。优选的磷酸二烷基酯是二(2-乙基己基)磷酸,合适的溶剂是煤油,石脑油,庚烷或其他与水不混溶的脂族烃。分离各相,并用少量稀盐酸洗涤含铀的有机相,并汽提例如。用氢氧化钠或氢氧化铵或碳酸盐溶液或浓盐酸处理。如果使用盐酸,则可将溶液蒸发至干,将生成的铀酰氯煅烧为U3O8,或蒸发以消除过量的盐酸(可循环使用),用水稀释,然后将铀沉淀成氨(如二铀酸铵),可以被煅烧成氧化物。

著录项

  • 公开/公告号GB856827A

    专利类型

  • 公开/公告日1960-12-21

    原文格式PDF

  • 申请/专利权人 UNION CARBIDE CORPORATION;

    申请/专利号GB19570029465

  • 发明设计人

    申请日1957-09-19

  • 分类号C01G43/00;C22B60/02;

  • 国家 GB

  • 入库时间 2022-08-23 18:23:19

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