Treatment of acid mine drainage: I. Equilibrium biosorption of zinc and copper on non-viable activated sludge

被引:72
作者
Utgikar, V
Chen, BY
Tabak, HH [1 ]
Bishop, DF
Govind, R
机构
[1] US EPA, Natl Risk Management Res Lab, Cincinnati, OH 45268 USA
[2] Univ Cincinnati, Dept Chem Engn, Cincinnati, OH 45221 USA
关键词
D O I
10.1016/S0964-8305(00)00053-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Biosorption is potentially attractive technology for treatment of acid mine drainage for separation/recovery of metal ions and mitigation of their toxicity to sulfate reducing bacteria. This study describes the equilibrium biosorption of Zn(II) and Cu(II) by nonviable activated sludge in a packed column adsorber. The Zn(II) uptake capacity of unconditioned sludge (not subjected to processing other than drying) was found to decrease in repeated adsorption-desorption cycles, declining by a factor greater than 20 from cycle 1 to cycle 6, Equilibrium uptake of metals by dried sludge conditioned by exposure to deionized water at a pH corresponding to that of the feed solution showed a strong pH dependence and was modeled using the Langmuir adsorption isotherm. Equilibrium metal uptakes from solutions containing single metal ion were 2.5 mg g(dry biomass)(-1) and 3.4 mg g(dry biomass)(-1) for Zn(II), and 1.9 mg g(dry biomass)(-1) and 5.9 mg g(dry biomass)(-1) for Cu(II) at pH 3.0 and 3.8, respectively. Equilibrium uptakes from binary mixtures were 30% lower than single component solution uptakes for both metals, indicating some competition between the two metals. No hysteresis was detected between adsorption and desorption equilibria. Anion concentration and pH measurements indicated that simultaneous sorption of metal cation and sulfate anion was probably occurring at pH 3.0, while proton exchange predominated at pH 3.8. Results of the study point to the usefulness of non-viable activated sludge as a biosorbent for recovery/separation of metal ions from acid mine drainages. Published by Elsevier Science Ltd.
引用
收藏
页码:19 / 28
页数:10
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