首页> 外国专利> Recovering of ruthenium, rhodium, palladium, osmium, iridium and platinum from precious metal containing solution by cathodic separation, comprises supplying the solution to cathode chamber and then separating or detaching the metal

Recovering of ruthenium, rhodium, palladium, osmium, iridium and platinum from precious metal containing solution by cathodic separation, comprises supplying the solution to cathode chamber and then separating or detaching the metal

机译:通过阴极分离从含贵金属的溶液中回收钌,铑,钯,,铱和铂,包括将溶液供应到阴极室,然后分离或分离金属

摘要

The procedure for recovering of ruthenium, rhodium, palladium, osmium, iridium and platinum from a precious metal containing solution by cathodic separation with the help of a electrolysis cell separated by a cation exchanger membrane, comprises supplying the solution to a cathode chamber, and then mechanically separating or electro-chemically detaching the precious metal. The separation is carried out with a current density of 10-50 mA/cm2 at a cathode potential of -240 to -280 mV related to the potential of a saturated calomel electrode at a temperature of 313-333 K. The procedure for recovering of ruthenium, rhodium, palladium, osmium, iridium and platinum from a precious metal containing solution by cathodic separation with the help of a electrolysis cell separated by a cation exchanger membrane, comprises supplying the solution to a cathode chamber, and then mechanically separating or electro-chemically detaching the precious metal. The separation is carried out with a current density of 10-50 mA/cm2 at a cathode potential of -240 to -280 mV related to the potential of a saturated calomel electrode at a temperature of 313-333 K and the electro-chemical separation is stopped, if redox potential, which is measured by silver/silver chloride-combined electrode, of the precious metal solution in the cathode chamber of the electrolysis cell is dropped to less than -100 mV related to the reference electrode. Anolyte nitric acid of concentration 1.5-5 Mol/liter is used as electrolytes, which flow throughable by the cathode- and anode ring of the respective electrode chamber. The base elements separated on the electrode are replaced by anodically dissolving in the nitric acid of the concentration 0.5-2.0 Mol/liter with a potential of 400-1000 mV referred on the potential of the calomel electrode. The palladium is obtained by anodically dissolving the metal precipitate with a potential of 1.0-1.2 V related to the potential of the calomel electrode in sulfuric acid of the concentration 0.5-1.5 Mol/liter nitric acid and 1.0-4.5 Mol/liter hydrochloric acid at a temperature of 313-343 K. The platinum is obtained by anodically dissolving the precipitate with a potential of 1200-1400 mV related to the potential of the calomel electrode in diluted aqua regia of the concentration 0.5-1.5 Mol/liter nitric acid and 1.0-4.5 Mol/liter hydrochloric acid at a temperature of 313-343 K. The rhodium is obtained by anodically dissolving in hydrobromic acid of the concentration 1-5 Mol/liter with a potential of 1000-1400 mV related to the potential of the calomel electrode. The separation takes place on an electrode, which is coated with diamond contaminated with boron. The distance between cathode and membrane is 2.5-5 mm and the cathode is coated by a plastic net. The cathodes are intended as sheet metals. The anodes are intended as sheet metals, perforated plates, expanded metal or fabrics. Spacers from plastic nets with an aperture greater than 60% are present between the electrodes and the membrane. The flow rate of the electrolytes in cathode and anode region is 0.1-10 cm/second. The precious metal components are crushed for the receipt of precious metal solution and disrupted by the extraction with a diluted acid mixture. The precious metal components are released by casing and isolation. The diluted aqua regia of the concentration 0.8-1.2 Mol/liter nitric acid and 2.5-3.5 Mol/liter hydrochloric acid is used for the extraction, which is carried out repeatedly in a temperature of 323-343 K for 4-14 hours. The decomposition solution is agitated while the extraction. Solids are separated from the decomposition solution. The separated solids with a quantity of less than 50% of their volume are washed at diluted aqua regia. The washing solution is added to the decomposition solution and the washing process is repetitively carried out. The cathodes and anodes are used on basis of titanium, niobium and tantalum, which are superficially coated with niobium, rhodium, tantalum, iridium and platinum or its alloys or its oxides.
机译:在通过阳离子交换膜分离的电解池的帮助下,通过阴极分离从含贵金属的溶液中回收钌,铑,钯,,铱和铂的步骤,包括将溶液供应至阴极室,然后机械分离或电化学分离贵金属。分离是在电流密度为10-50 mA / cm2的情况下,在-240至-280 mV的阴极电势下进行的,该电势与温度为313-333 K的饱和甘汞电极的电势有关。借助借助阳离子交换器膜分离的电解池,通过阴极分离从含贵金属的溶液中分离钌,铑,钯,,铱和铂,包括将溶液供应至阴极室,然后进行机械分离或电解-化学分离贵金属。分离是在10-40 mA / cm2的电流密度下,在-240至-280 mV的阴极电势下进行的,该电势与温度为313-333 K的饱和甘汞电极的电势和电化学如果通过电解银阴极室中的贵金属溶液的贵金属溶液的氧化还原电势(通过银/氯化银复合电极测得)相对于参比电极下降到小于-100 mV,则停止分离。浓度为1.5-5 Mol / L的阳极电解液硝酸用作电解质,可通过相应电极室的阴极和阳极环流通。电极上分离的基础元素被阳极溶解在浓度为0.5-2.0 Mol /升的硝酸中,电位为甘汞电极的电势为400-1000 mV。通过将与甘汞电极的电势相关的电势为1.0-1.2 V的金属沉淀物阳极溶解在浓度为0.5-1.5 Mol / L的硝酸和1.0-4.5 Mol / L的硫酸中,从而获得钯。温度为313-343K。通过将沉淀物阳极溶解在浓度为0.5-1.5 Mol /升硝酸和1.0稀稀王水中的与甘汞电极电位相关的1200-1400 mV的电位下获得铂。 -4.5摩尔/升盐酸,温度为313-343K。铑是通过将1-5摩尔/升的氢溴酸阳极溶解在与甘汞电位相关的1000-1400 mV的电位上而制得的电极。分离在电极上进行,电极上涂有被硼污染的金刚石。阴极和膜之间的距离为2.5-5 mm,阴极用塑料网覆盖。阴极用作金属板。阳极用作金属板,穿孔板,金属网或织物。电极和膜之间存在塑料网的垫片,其孔径大于60%。阴极和阳极区域中的电解质的流速为0.1-10cm /秒。压碎贵金属成分以接收贵金属溶液,并通过用稀酸混合物萃取来打碎。贵金属成分通过包装和隔离释放。使用浓度为0.8-1.2摩尔/升硝酸和2.5-3.5摩尔/升盐酸的稀王水进行萃取,萃取在323-343 K的温度下重复进行4-14小时。提取时搅拌分解液。从分解溶液中分离出固体。数量少于其体积50%的分离出的固体在稀释王水上洗涤。将洗涤溶液添加到分解溶液中,并且重复进行洗涤过程。阴极和阳极以钛,铌和钽为基础,钛,铌和钽表面覆盖有铌,铑,钽,铱和铂或其合金或氧化物。

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