摘要:
An industrial waste salt resourceful treatment method comprises the following steps: the industrial waste salt is sequentially subject to dissolving, chemical pre-purification, deep purification, organic matter concentration reduction, adsorption and oxidation decolorization and multi-effect evaporative crystallization to respectively obtain sodium sulfate, sodium chloride and sodium nitrate crystals; the crystallization temperature of sodium sulfate is in a range of 75° C. to 85° C.; the crystallization temperature of sodium chloride is in a range of 60 to 70° C.; and the crystallization temperature of sodium nitrate is in a range of 45° C. to 55° C. An industrial waste salt resourceful treatment device is further provided.
摘要:
A process for treating wastewater or waste brines that include sodium and chloride ions. The waste brine is concentrated and thereafter directed to a Mirabilite crystallizer that produces hydrated sulfate salt crystals and a first solution. The hydrated crystals are melted to form an aqueous sulfate solution that is directed to a sodium sulfate crystallizer which produces sodium sulfate salt crystals. The first solution produced by the Mirabilite crystallizer is directed to a nanofiltration device which produces a permeate stream and a reject stream containing sulfate removed by the nanofiltration device. The permeate stream is directed to a sodium chloride crystallizer that produces sodium chloride salt crystals. The reject stream is recycled to the Mirabilite crystallizer.
摘要:
There are provided methods for the production of potassium sulphate. The methods comprise contacting an aqueous potassium- and sulphate-containing composition with magnesium chloride (MgCl2), thereby obtaining a composition comprising kainite; optionally concentrating the kainite from the composition; reacting the kainite with magnesium sulphate (MgSO4) and potassium sulphate (K2SO4) so as to convert the kainite into leonite (K2SO4.MgSO4.4H2O); optionally contacting the leonite with water to remove excess MgSO4 and contacting the leonite with water so as to leach the MgSO4, contained in the leonite, and to at least substantially selectively precipitate potassium sulphate (K2SO4), and further involving a process brine sulphate control step, based on bloedite precipitation, to control the overall level of sulphate in the method. The method according to the invention can be operated at higher temperatures, in particular at temperatures above 35° C. and does not require a cooling step at 20 to 25° C. The method produces potassium sulphate with a low amount of chloride.
摘要:
A process employing a fixed-resin bed Acid Retardation Unit (ARU) to separate spent acid from chlorine dioxide generators into a de-acidified sodium sulfate component and a purified sulfuric acid component. The de-acidified sodium sulfate produced is returned to the chemical recovery cycle of the kraft mill in place of acidic chlorine dioxide generator effluent thereby avoiding the destruction of alkalinity in pulp mill liquors. In addition, sulfuric acid is purified providing an opportunity for reuse in various mill applications, and/or concentrated and recycled to the generator. Alternatively, to avoid high evaporation costs, the purified acid can be used to regenerate a cation-exchange unit (CEU) used in the conversion of sodium chlorate to a sodium chlorate/chloric acid mixture which is fed to the generator in place of sodium chlorate and sulfuric acid. Using this approach, the sulfuric acid requirement of chlorine dioxide generators and, in turn, the amount of acidic generator effluent can be reduced. The process is applicable to both atmospheric and subatmospheric chlorine dioxide generators. In the latter case, the concentration of the purified sulfuric acid from the ARU or any other acid separation system can be increased by using a portion of it to dissolve the sodium sesquisulfate by-product from such generators.
摘要:
Disclosed is a process for making orthorhombic Na.sub.2 SO.sub.4 containing less than 0.1 ppm chromium from a solution of Na.sub.2 SO.sub.4 containing 0.1 to 100 ppm Cr(III). The Cr(III) is oxidized to Cr(VI) at a pH greater than 7, water is evaporated from the solution to precipitate the orthorhombic Na.sub.2 SO.sub.4, and the precipitated orthorhombic Na.sub.2 SO.sub.4 is separated from the solution.
摘要翻译:公开了从含有0.1至100ppm Cr(III)的Na 2 SO 4溶液中制备含有小于0.1ppm铬的正交Na 2 SO 4的方法。 在大于7的pH下将Cr(III)氧化成Cr(VI),从溶液中蒸发水以沉淀正交的Na 2 SO 4,并将沉淀的正交Na 2 SO 4与溶液分离。
摘要:
In a purification process for brine, impurities such as calcium, magnesium and/or sulphate are precipitated by the addition of calcium hydroxide (Ca(OH).sub.2) and sodium carbonate (Na.sub.2 CO.sub.3). Following NaCl crystallization by evaporation of the brine, a mother liquor is obtained which still contains among others sulphate, potassium and bromide ions. Further concentration of this mother liquor by evaporation results in the precipitation of both NaCl and Na.sub.2 SO.sub.4 and a more strongly concentrated mother liquor with respect to both potassium and bromide remains. This concentrated mother liquor is drained off. Either the precipitated NaCl and Na.sub.2 SO.sub.4 are dissolved in water or the Na.sub.2 SO.sub.4 is dissolved in purified brine or crude brine and then returned to the brine purification process, thereby lowering both the potassium and bromide ion levels in the purified brine. As a consequence the contents of both potassium and bromide of the NaCl are reduced.
摘要:
A method for removing magnesium and calcium from sodium sulfate solutions to render the solutions suitable for membrane processing, which comprises adjusting the pH of the solutions to about 11 to 13 with sodium hydroxide to form a precipitate containing the bulk of the magnesium and the calcium, removing the precipitate from the resulting partially purified sodium sulfate solution, and contacting the partially purified sodium sulfate solution with a polystyrene divinyl benzene copolymer chelating cation exchange resin having an aminophosphonic functional group and having sodium as the exchangeable cation, to remove essentially all of the magnesium and the calcium from the partially purified sodium sulfate solution.
摘要:
Process of purification of magnesic raw material. Sulphur dioxide is allowed to react with an aqueous suspension of calcinated magnesite, crude or contaminated magnesium oxide, magnesium hydroxide, hydrated magnesium carbonates, or crude crystals of magnesium sulphite, and, after reaching a pH of 3 to 7.5 the reaction mixture is separated into a solid phase at least one fraction of which is rich in MgSO.sub.3.xH.sub.2 O, wherein x stands for 3 or 6, and at least one fraction containing concentrated impurities. The whole process is carried out at least once. A reaction mixture having a pH below 5 can be preferably transferred to pH 5.2 by the addition of an alkali, e.g. magnesium oxide or magnesium hydroxide, whereupon separation of at least two fractions of the solid phase is accomplished. The fractions obtained can be further purified by mixing in a hydrophilic liquid, and by a following separation. The fraction of crude magnesium sulphite crystals can be heated to a temperature over 60 degress C., preferably to 90 to 100 degrees C., whereupon the solution containing magnesium sulphite is separated from solid impurities, or the treated mixture is cooled to a temperature below 60 degrees C. and solid phases are separated into one or more fractions rich in MgSO.sub.3.xH.sub.2 O and to one or more fractions mainly containing impurities. Filtration, sedimentation, or centrifugation can be used for the separation.