羟肟萃取剂LIX984N酸解和铜萃取分相性能

铜溶剂萃取时,萃取剂与硫酸溶液接触将促发其降解。研究羟肟萃取剂LIX984N的酸解行为及其对萃取分相性能的影响。结果表明:酸降解使肟基结构破坏,LIX984N中5-壬基水杨醛肟降解生成2-羟基-5-壬基苯甲醛、2-羟基-5-壬基乙酰苯酮肟降解生成2-羟基-5-壬基苯甲酮;有机相与浓硫酸溶液接触30 h后,萃余液表面张力从56.4 m N/m降至38.1 m N/m,铜萃取分相速率明显降低,萃余液中有机相夹带量、溶解量显著增大,有机相流失现象加重。研究发现夹带是萃余液中有机相流失的主要形式,接触50 h时夹带量在有机相流失总量中占61%。

BL-SX-EW工艺中萃取界面乳化现象成因研究

德兴铜矿生物浸出 溶剂萃取 电积铜生产中 ,在溶剂萃取界面产生严重的乳化现象 ,致使整个生物冶铜工艺运行状况恶化。通过对界面乳化物特性进行系统研究 ,认为乳化物的生成是由有机相中杂质和降解产物 ,以及萃取过程中的沉淀物和萃原液中固体悬浮物引起。同时 。

Optimization of separation processing of copper and iron of dump bioleaching solution by Lix 984N in Dexing Copper Mine

The effects of the concentration of Lix 984N,phase ratio,initial pH value of aqueous phase and extraction time on the extraction of copper and iron under the condition of low Cu2+ /Fe3+ ratio in dump bioleaching solution of Dexing Copper Mine were explored.The optimal conditions of extraction are as follows: the concentration of Lix 984N 10%; the phase ratio (O/A) 1:1; the initial pH value of aqueous phase 1.5 and the mixing time 2 min.The stripping experiments show that H2SO4 solution could efficiently recover copper from the organic phase under the optimal conditions.

Recovery of Copper（II） and Nickel（II） from Plating Wastewater by Solvent Extraction

The solvent extraction technology, was applied to recover Cu^2＋ and Ni^2＋ from plating wastewater.Lix984N was chosen as the extractant due to-its gooff extraction performance. The influence parame-ters were examlned. The results show that the separation of Cu^2＋ and Ni＂ from sulphate medium can be realized by adjusting pH value with the help of Lix984N. For extracting Cu^2＋ and Ni^2＋, the optimal pH values are 4 and 10.5, and the maximal extraction percentages are 92.9% and 93.0%, respectively .With recovered Cu^2＋ and Ni^2＋ stripped in 170g.L^ -1 and 200 g.L^-1 H2SO4 medium, the stripping percentages of Cu^2＋ and Ni^2＋ are 92.9% and 93.0%, respectively. This method is simple and can be used to recover Cu^2＋ and Ni^2＋ from plating wastewater. And a flow sheet for separation of Cu^2＋ and Ni^2＋ is presented.

Recovery of nickel,cobalt,copper and zinc in sulphate and chloride solutions using synergistic solvent extraction

A number of synergistic solvent extraction （SSX） systems have been developed to recover nickel, cobalt, zinc and copper from sulphuric and chloride leach solutions by the solvent extraction team of CSIRO, Australia. These in- clude （1） Versatic 10/CLXS0 system for the separation of Ni from Ca in sulphate solutions, （2） Versatic 10/4PC system for the separation of Ni and Co from Mn/Mg/Ca in sulphate solutions, （3） Cyanex 471X/HRJ-4277 system for the separation of Zn from Cd in sulphate solutions, （4） Versatic 10/LIX63 system for the separation of Co from Mn/Mg/Ca in sulphate solutions, （5） Versatic 10/LIX63/TBP system for separation of Ni and Co from Mn/Mg/Ca in sulphate solutions, （6） Versatic 10/LIX63 system for the separation of cobalt from nickel in sulphate solutions by difference in kinetics, （7） Cyanex 272/LIX84 system for the separation of Cu/Fe/Zn from Ni/Co in sulphate solutions, （8） Versatic 10/LIX63fFBP system to recover Cu/Ni from strong chloride solutions, and [9） Versatic 10/LIX63 system to separate Cu from Fe in strong chloride solutions. The synergistic effect on metal separation and efficiency is presented and possible industrial applications are demonstrated. The chemical stability of selected SSX systems is also reported.

Copper solvent extraction from alkaline cyanide solution with guanidine extractant LIX 7950

The use of the guanidine extractant LIX 7950 extracting copper and cyanide from alkaline cyanide solution was investigated.The extraction of copper and cyanide under different initial copper and extractant concentrations was examined and the stoichiometric extraction constant of Cu(CN)32- with LIX 7950 was calculated.Both the distribution coefficient and the stoichiometric extraction constant of Cu(CN)3 2-with LIX 7950 decrease when the temperature is varied from 25℃to 45℃, indicating the extraction process is exothermic.The calculated enthalpy change of the reaction(-HΘ)is about-190 kJ/mol.The copper extraction isotherms under different molar ratios of cyanide to copper are established.The preferential extraction of Cu(CN)32- over Cu(CN)4 3-and CN -has been confirmed and a high cyanide-to-copper molar ratio tends to suppress copper loading. The loaded copper and cyanide can be stripped efficiently by the moderately strong NaOH solutions(0.5-1.0 mol/L)and the presence of NaCN in the stripping solution facilitates copper stripping.

Extraction and stripping of Cu and Ni from synthetic and industrial solutions of Sarcheshmeh Copper Mine containing Cu, Ni, Fe and Zn ions

The extraction and stripping of Cu and Ni ions from synthetic and industrial solutions of Sarcheshmeh Copper Mine containing Cu(770 mg/L),Ni(3200 mg/L),Fe(800 mg/L)and Zn(200 mg/L)were comprehensively investigated using D2 EHPA,LIX 984,Cyanex 302,Chemorex CP 150 and Acorga 5774 diluted in kerosene.The influential parameters such as mixing speed and time,concentration of extractant,p H and temperature were considered in extraction stage.Furthermore,stripping of Cu and Ni was examined using different inorganic and organic acids(sulfuric,hydrochloric,nitric and citric acids)with different concentrations.The results indicated that the highest extractions of Cu and Ni occurred within 3 min,with the mixing speed of 500 r/min,28℃and A/O ratio of 1:1.Moreover,Cu was extracted by LIX 984 at the concentration of 10%(v/v),whereas Ni was extracted by Cyanex 302 at the concentration of 30%(v/v),efficiently.The optimal p H for Cu and Ni extraction is in ranges of 2-3 and 4-5,respectively.Cu and Ni were selectively extracted with the recoveries of 85%,93%and 77%,82%from synthetic and industrial solutions containing Ni,Cu,Zn and Fe ions,respectively.The results of optimal condition showed that 96%of Ni and 93%of Cu were stripped from the synthetic and industrial solutions.Finally,four elements Zn,Fe,Cu and Ni were extracted in three stages with D2 EHPA,LIX 984 and Cyanex 302 extractants respectively with the least impurities.

Degradation of Lix984N and its effect on interfacial emulsion

The organic phase separated from the interfacial crud provided by Dexing copper mine in Jiangxi, China, was analyzed by combined gas chromatography-mass spectroscopy. The results show that many kinds of emphiphiles containing such hydrophilic groups as carbonyl, carboxyl, sulphonyl or acylamine exist in organic phase. Conclusively, Lix984N would degrade gradually during a long-term contact with the acidic aqueous feed and strip reagents. Lix84 and nonylphenol as effective components of Lix984N degraded almost completely after long-term recycling. Lix984N degraded through such reactions as Beck.mann rearrange, hydrolysis and sulphofication. The degradation of Lix984N would deteriorate solvent extraction and disengagement performance, and result in a more stable interracial emulsion.

Selective extraction of gold(Ⅲ) from hydrochloric acid-chlorine gas leach solutions of copper anode slime by tri-butyl phosphate(TBP)

The oxidative leaching causes to dissolve various impurities such as Fe, Cu, Pd, Se in copper anode slime. Organicextractant tri-butyl phosphate (TBP) was used to purify leach solution. Several parameters, such as TBP, HCl and chloride inorganicsalt concentrations were chosen in order to determine efficient state for impurities separation. Standard solvent extraction tests forextraction and separation of Au, Pd, Pt, Fe, Cu and Se were conducted with equal volume of aqueous and organic phases in batchexperiments. The effect of hydrochloric acid, organic phase and metals initial concentration were examined at ambient temperature. Itwas found that 0.25 mol/L TBP in the presence of 2.5 mol/L hydrochloric acid can cause high extraction of gold. Meanwhile, in theseconditions the extraction of other impurities is negligible. After extraction, pregnant organic phase was scrubbed by distilled waterand some impurities were removed. Finally, gold was stripped by sodium thiosulfate solution. The stripping solution does not haveany impurities. By adding H2SO4 to stripping solution containing Na2S2O2, SO2 gas is released and Au3+ ions could be reduced.

Selective separation of copper and cadmium from zinc solutions by low current density electrolysis

Copper and cadmium ions were selectively separated from zinc sulphate aqueous solution or zinc ammonia/ammonium sulphate aqueous solution by low current density electrolysis.It was shown that the concentration of cadmium ion in zinc sulphate solution decreased from 4.56 g/L to 0.18 g/L in an electrolysis time of 8.5 h,whilst it decreased from 5.16 g/L to lower than 0.005 g/L in zinc ammonia/ammonium sulphate aqueous solution.On the other hand,the deposition rate of copper was so low that it was difficult to separate copper and cadmium ions from the zinc ammonia/ammonium sulphate aqueous solution during electrolysis.But copper ion could be decreased to 0.002 g/L in this solution through solvent extraction by using kerosene diluted LIX984N as extractant.Therefore,it is favorable to recover cadmium ion from the zinc ammonia/ammonium sulphate solution by electrolysis after solvent extraction of copper.

Solvent extraction of copper and zinc from bioleaching solutions with LIX984 and D2EHPA

The solvent extraction of copper and zinc from the bioleaching solutions of low-grade sulfide ores with LIX984 and D2EHPA was investigated. The influences of extractant content, aqueous pH value, phase ratio and (equilibration) time on metals extraction were studied. The results show that LIX984 has a higher selectivity for copper than for iron, zinc and other metals, and has the copper extraction rate above 97%, while the zinc and iron extraction rate is less than 1.6% respectively. Zinc extraction is carried out following the copper extraction from the raffinate. The zinc extraction with di(2-ethylhexyl) phosphoric acid(D2EHPA) is low due to its poor cation exchange. A sodium salt of D2EHPA is used and the zinc extraction rate is enhanced to above 98%. Though iron (Ⅲ) is strongly extracted before the extraction of zinc by D2EHPA, it is difficult to strip iron from the organic phase by sulfuric acid. The zinc stripping rate is above 99% with 100g/L sulfuric acid, while that of iron is 0.16%. Hence, the separation of zinc from iron can be achieved by the selective stripping.

Solvent extraction of copper and ammonia from ammoniacal solutions using sterically hindered β-diketone

Extraction of copper and ammonia from Cu2+-NH3-Cl--H2O solution using laboratorialy synthesized sterically hindered β-diketone(4,4-dimethyl-1-(4-dodecylphenyl)-1,3-pentanedione) was studied.The effects of the copper concentration,the total ammonia concentration,the initial pH in the aqueous phase,the phase ratio,and the temperature on copper extraction ratio and ammonia extraction in loaded organic phase were investigated using this sterically hindered β-diketone.Under the conditions of temperature 25℃,contact time of two phases 30 min,phase ratio 1-1,concentration of copper 3 g/L,concentration of total ammonia 3 mol/L,aqueous pH 8.43,and the concentration of β-diketone in organic phase 20%(volume fraction),ammonia in aqueous phase is much lower to be extracted by organic phase(just 14.5 mg/L),while the extraction rate of copper is 95.09%.