Deepatana A, Valix M
Department of Chemical Engineering, The University of Sydney, Sydney 2006, NSW, Australia.
J Hazard Mater. 2006 Sep 21;137(2):925-33. doi: 10.1016/j.jhazmat.2006.03.015. Epub 2006 May 15.
This study examined the recovery of nickel and cobalt from organic acid complexes using a chelating aminophosphonate Purolite S950 resin. These metal complexes are generated by bioleaching nickel laterite ores, a commercial nickel and cobalt mineral oxide, with heterotrophic organism and their metabolites or organic acid products. Equilibrium adsorption tests were conducted as a function of Ni and Co concentrations (15-2000 mg/L), solution pH (0.01 and 0.1 M acids) and three metabolic complexing agents (citrate, malate and lactate). It was shown that the adsorption of the various Ni- and Co-complexes on Purolite were quite low, 16-18 and 5.4-9 mg/g of resin, respectively, in comparison to the smaller nickel ions and nickel sulfate. This was attributed to the bulky organic ligands which promoted crowding effect or steric hindrance. The adsorption of these complexes was further hampered by the strong affinity of the resin to H+ ions under acidic conditions. Mechanisms of adsorption, as inferred from the fitted empirical Langmuir and Freundlich models, were correlated to the proposed steric hindrance and competitive adsorption effects. Nickel and cobalt elution from the resin were found be effective and were independent of the type of metal complexes and metal concentrations. This study demonstrated the relative challenges involved in recovering nickel and cobalt from bioleaching solutions.
本研究考察了使用螯合氨基膦酸Purolite S950树脂从有机酸络合物中回收镍和钴的情况。这些金属络合物是通过用异养生物及其代谢产物或有机酸产物对商业镍钴矿物氧化物红土镍矿进行生物浸出而生成的。进行了平衡吸附试验,考察了镍和钴浓度(15 - 2000 mg/L)、溶液pH值(0.01和0.1 M酸)以及三种代谢络合剂(柠檬酸盐、苹果酸盐和乳酸盐)的影响。结果表明,与较小的镍离子和硫酸镍相比,各种镍和钴络合物在Purolite树脂上的吸附量相当低,分别为16 - 18 mg/g和5.4 - 9 mg/g树脂。这归因于庞大的有机配体促进了拥挤效应或空间位阻。在酸性条件下,树脂对H⁺离子的强亲和力进一步阻碍了这些络合物的吸附。从拟合的经验朗缪尔和弗伦德利希模型推断出的吸附机制与所提出的空间位阻和竞争吸附效应相关。发现从树脂中洗脱镍和钴是有效的,并且与金属络合物的类型和金属浓度无关。本研究证明了从生物浸出溶液中回收镍和钴所涉及的相关挑战。