摘要:
A method of purifying phosphoric acid after solvent extraction to remove residual amounts of an immiscible organic carrier including contacting the phosphoric acid with a sorbent which sorbs or takes up the residual amount of organic carrier and separating the phosphoric acid from the organic carrier-laden sorbent. The method is especially suitable for removing residual organic carrier from phosphoric acid after solvent extraction uranium recovery.
摘要:
An organic phase including both phosphoric acid and sulfuric acid is purified of sulfate ion content by countercurrently washing same with an aqueous liquid in an at least two-stage wash zone, the pH of which having been adjusted with an alkali metal or ammonium compound to a value greater than that as would exist if the washing were effected with the aqueous liquid alone, under the same conditions, and whereby there results a purified organic phase comprising both SO.sub.4 and P.sub.2 O.sub.5 in an amount by weight of SO.sub.4 to P.sub.2 O.sub.5 of less than 50 ppm.
摘要翻译:包括磷酸和硫酸的有机相通过在至少两级洗涤区中的水性液体逆流洗涤来纯化硫酸根离子含量,所述至少两个阶段的洗涤区的pH用碱金属或铵化合物调节至 如果在相同条件下仅用水性液体进行洗涤即可存在,其结果是SO 4和P 2 O 5的纯化有机相的SO 4和P 2 O 5的重量比小于50ppm 。
摘要:
Contaminated phosphoric acid, particularly wet-processed phosphoric acid, is purified by extracting it from its aqueous solution by means of an organic solvent, which is immiscible or partially miscible with water and in which phosphoric acid is soluble, separating the phosphoric acid being dissolved in the organic solvent from extraction residue, and recovering the phosphoric acid from the organic solution.The aqueous phosphoric acid is more particularly mixed in a reaction zone, in a ratio by volume within the range 1:0.3 to 1:30, with a solvent having a boiling point higher than that of water or higher than that of the resulting water solvent-azeotrope, the phosphoric acid/solvent-mixture is heated to temperatures between the boiling point of water or of the said azeotrope and that of the solvent until distillation of substantially all uncombined water originally present in the mixture, and residue and resulting anhydrous phosphoric acid solution in the organic solvent are separated.
摘要:
There is disclosed a countercurrent multi-stage process for separating an organic solvent from a phosphoric acid solvent solution by the addition of an alkali material such that the ratio of Na.sub.2 O to P.sub.2 O.sub.5 in the water phase in each stage is from 0.45:1 to 0.90:1 whereby substantially all the organic solvent is recovered from the starting solution in the final stage of the extractor.
摘要:
There is provided a process for preparing a crystalline electrode material, the process comprising: providing a liquid bath comprising the electrode material in a melted state; and introducing a precursor of the electrode material into the liquid bath, wherein the electrode material comprises lithium, a metal and phosphate. There is also provided a crystalline electrode material, comprising lithium substituted by less than 0.1 atomic of Na or K; Fe and/or Mn, substituted by less than 0.1 atomic ratio of: (a) Mg, Ca, Al and B, (b) Nb, Zr, Mo, V and Cr, (c) Fe(III), or (d) any combinations thereof; and PO4, substituted by less than 20% atomic weight of an oxyanion selected from SO4, SiO4, BO4, P2O7, and any combinations thereof, the material being in the form of particles having a non-carbon and non-olivine phase on at least a portion of the surface thereof.
摘要:
An arrangement (100) for production of fully soluble, pure and well defined mono- or di-ammonium phosphates, comprises an extraction section (10), a stripping section (20) and end treatment arrangements (90). The extraction section performs a liquid-liquid extraction of phosphate between a feed liquid (1) comprising phosphoric acid and being essentially free from nitrate ions, and a solvent (5) having a solubility in water of less than 2%. The stripping section performs a liquid-liquid extraction of phosphate between solvent loaded with phosphate and a strip solution (4). The solvent depleted in phosphate is recirculated to the extraction section for further extraction of phosphate. The strip solution is an aqueous ammonium phosphate solution, wherein at least 80% of the ammonium phosphate is monoammonium phosphate and/or wherein the solvent is a water-immiscible alcohol. The end treatment arrangements comprise a source of ammonia (60), an adding arrangement (70), a cooling arrangement (50), a precipitate remover (40) and a recirculation system (80).
摘要:
A method for removing organic materials dissolved in purified phosphoric acid by decomposing it with hydrogen peroxide, characterized in that after the treatment with hydrogen peroxide, the purified phosphoric acid is contacted with reducing phosphorus compounds.
摘要:
A process is developed for producing phosphoric acid and phosphates from wet-process phosphoric acid. The crude acid is extracted with a waterimmiscible solvent mixture consisting of mixed trialkyl phosphine oxide and a diluent, wherein about 2/3 P.sub.2 O.sub.5 in the crude acid is extracted into solvent mixture and the balance remains in the raffinate. Pure phosphoric acid or phosphates are produced by stripping the loaded solvent with appropriate aqueous phase and secondary calcium phosphate fertilizer is obtained by neutralizing the raffinate with calcium carbonate.
摘要翻译:开发了一种从湿法磷酸生产磷酸和磷酸盐的工艺。 粗酸用与混合的三烷基氧化膦和稀释剂组成的水混溶性溶剂混合物萃取,其中将粗酸中的约2/3 P 2 O 5萃取到溶剂混合物中,余量保留在萃余液中。 通过用适当的水相汽提负载的溶剂来制备纯磷酸或磷酸盐,通过用碳酸钙中和萃余液获得二次磷酸钙肥料。
摘要:
The invention is a process to purify a solution of phosphoric acid by removing transition metal impurities such as iron, chromium and vanadium. In the process a solution of phosphoric acid in an organic solvent which is substantially immiscible with water is contacted with an aqueous solution of a salt of an alkali metal of phosphoric acid. The phosphoric acid recovered following the contacting contains a substantially lesser content of transition metal impurities.
摘要:
Disclosed is a process for the precipitation and separation of cadmium sulphide from the raffinates derived from phosphoric acid purification by treating the cadmium containing streams of the raffinates with a H.sub.2 S containing solvent phase in a mixing-settling apparatus, by separating the raffinate phase from the cadmium sulphide containing solvent phase and by separating the precipitated cadmium sulphide from the solvent phase. By operating this process it is possible to remove cadmium in a simple manner from the raffinates since their inherent properties don't influence the precipitation and separation of cadmium sulphide.