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The manufacture of phosphorus oxychloride addition products and their use for separating niobium and tantalum from mixtures containing them

机译:氯氧化磷加成产物的生产及其在从含铌和钽的混合物中分离铌和钽的用途

摘要

An addition product of tantalum or niobium pentachloride and phosphorus oxychloride is prepared by contacting the constituents under anhydrous conditions. Amongst the products, compounds having a ratio of metal pentachloride to phosphorus oxychloride of 1:1 are formed. Tantalum and niobium may be separated by fractional distillation of the addition products. The pentachloride may be reacted with phosphorus oxychloride by dissolution of solid or gaseous pentachloride in the liquid oxychloride at ordinary or elevated temperature, excess oxychloride being then removed by distillation at 100-200 DEG C. at atmospheric pressure or by reacting phosphorus oxychloride vapour (or an inert gas containing phosphorus oxychloride vapour) with the solid pentachlorides, preferably at above the meltingpoint of the addition products, i.e. at 100-180 DEG C., or with the pentachloride in gaseous form, e.g. when leaving a chlorination zone. An initial mixture of halides may be obtained by briquetting slags, concentrates or ores containing niobium and tantalum in oxidized form with carbon and chlorinating with chlorine gas at 400-1000 DEG C.; if the products contain niobium oxychloride they are further chlorinated in the presence of carbon to convert the oxychloride to pentachloride. Chlorides such as silicon, titanium, tin and manganese chlorides may thereafter if desired be at least partly removed by condensing the mixture under suitable conditions. Alternatively, the initial mixture may be prepared by treating niobium and tantalum oxides with phosphorus pentachloride at 200 DEG C. in the absence of air or moisture or with a current of dry carbon tetrachloride or by chlorinating an alloy of niobium and tantalum. If the crude chlorination gases are dissolved in phosphorus oxychloride, addition products with zirconium and titanium chlorides separate in crystalline form and may be removed. The niobium and tantalum addition products may, if desired, be subjected to a preliminary distillation to remove other metals. The separation of niobium and tantalum by fractional distillation may be carried out under reduced pressure or under atmospheric pressure with the exclusion of moisture and in air or an inert gas such as nitrogen or carbon dioxide. The tantalum product has the higher boiling-point. Zirconium, aluminium and iron chloride addition products, if present, remain in the residue. It is desirable to add to the mixture before distillation an inert substance boiling above the tantalum pentachloride addition product, e.g. the addition product with aluminium chloride (or aluminium trichloride itself). If desired the products may be redistilled, and the pentachlorides then recovered by adding the addition products to a solvent at room temperature or an elevated temperature. Suitable solvents are those which dissolve or form addition products with phosphorus oxychloride without decomposing and in which the tantalum and niobium pentachlorides are insoluble, e.g. liquid hydrocarbons and carbon tetrachloride, chloroform and chlorobenzene, and solvents which form new addition products with niobium and tantalum pentachlorides which are insoluble in the solvent and unstable at raised temperatures, e.g. ethyl ether, ethyl acetate and acetone. The phosphorus oxychloride formed may be separated, e.g. by distillation, and re-used in forming further quantities of reaction product and the process made cyclic. Examples are given in some of which in addition to the metals mentioned above, silicon, manganese and tungsten are mentioned as being present in the addition products.
机译:钽或五氯化铌与三氯氧化磷的加成产物是通过在无水条件下使各组分接触而制备的。在这些产物中,形成五氯化金属与三氯氧化磷之比为1:1的化合物。可以通过分馏加成产物来分离钽和铌。通过在常温或高温下将固体或气态五氯化物溶解在液态氯氧化物中,可以使五氯化物与三氯氧化磷反应,然后通过在大气压下于100-200℃下蒸馏或通过使三氯氧化氯蒸气反应(或(一种含有三氯氧化磷蒸气的惰性气体)与固态的五氯化物,优选在加成产物的熔点以上,即100-180℃,或与五氯化物呈气态,例如离开氯化区时。卤化物的初始混合物可以通过将含铌和钽的氧化形式的碳,铌和钽的矿渣,精矿或矿石压块并在400-1000℃下用氯气进行氯化而得到。如果产品包含三氯氧化铌,则将它们在碳存在下进一步氯化以将三氯氧化氯转化为五氯化碳。如果需要,此后如果需要,可以通过在合适的条件下冷凝混合物来至少部分除去氯化物,例如硅,钛,锡和锰的氯化物。或者,可以通过在无空气或湿气的情况下在200℃下用五氯化磷处理铌和钽的氧化物或用干燥的四氯化碳气流或通过氯化铌和钽的合金来制备初始混合物。如果将粗氯化气溶解在三氯氧化磷中,则含有锆和氯化钛的加成产物会分离成结晶形式,并且可以除去。如果需要,可以将铌和钽的加成产物进行初步蒸馏以除去其他金属。通过分馏分离铌和钽的步骤可以在减压或大气压下进行,不包括水分,在空气或惰性气体(如氮气或二氧化碳)中进行。钽产物具有较高的沸点。残留的锆,铝和氯化铁加成产物(如果存在)。希望在蒸馏之前将沸点高于五氯化钽加成产物的惰性物质,例如碳酸氢钠,加到混合物中。加入产物与氯化铝(或三氯化铝本身)。如果需要,可以将产物再蒸馏,然后通过将添加产物在室温或高温下添加到溶剂中来回收五氯化物。合适的溶剂是那些能与三氯氧化磷溶解或形成加成产物而不分解的溶剂,其中五氯化钽和五氯化铌不溶于其中,例如氯化钠和氯化铌。液态烃和四氯化碳,氯仿和氯苯,以及与五氯化铌和五氯化钽形成新加成产物的溶剂,该五氯化铌和五氯化钽不溶于该溶剂,并且在高温下不稳定,例如乙醚,乙酸乙酯和丙酮。可以分离形成的三氯氧化磷,例如将其分离。通过蒸馏,再用于形成更多数量的反应产物,并使该过程循环。给出了一些例子,其中除了上述金属之外,还提到了硅,锰和钨存在于加成产物中。

著录项

  • 公开/公告号GB833569A

    专利类型

  • 公开/公告日1960-04-27

    原文格式PDF

  • 申请/专利权人 CIBA LIMITED;

    申请/专利号GB19570009025

  • 发明设计人

    申请日1957-03-19

  • 分类号C01G33/00;

  • 国家 GB

  • 入库时间 2022-08-23 19:04:55

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