Selective membrane alternative to the recovery of zinc from hot-dip galvanizing effluents

被引:53
|
作者
Carrera, J. A. [1 ]
Bringas, E. [1 ]
Roman, M. F. San [1 ]
Ortiz, I. [1 ]
机构
[1] Univ Cantabria, ETSII & T, Dept Chem Engn & Inorgan Chem, E-39005 Santander, Spain
关键词
Emulsion pertraction; Zinc recovery; Hollow fiber; Tributyl phosphate; Spent pickling effluents; SUPPORTED LIQUID-MEMBRANE; EMULSION PERTRACTION PROCESS; HYDROCHLORIC-ACID SOLUTIONS; SPENT PICKLING SOLUTIONS; SOLVENT-EXTRACTION; NONDISPERSIVE EXTRACTION; BACK-EXTRACTION; MASS-TRANSFER; SEPARATION; REMOVAL;
D O I
10.1016/j.memsci.2008.11.002
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This work reports the study of the kinetics of zinc recovery from spent pickling solutions by means of emulsion pertraction technology (EPT) in order to reuse the metal in electrolytic processes. Tributyl phosphate (TBP) and service water were used as extraction (EX) and back-extraction (BEX) agents, respectively. Kinetic experiments were carried out in hollow fiber membrane contactors in order to analyse the influence of several operation variables on the rate of zinc recovery. A mathematical model that considers the mass transfer resistance shared between the organic liquid membrane and the organic phase boundary layer was developed; the mass transfer coefficients were estimated by means of the parameter estimation tool ASPEN CUSTOM MODELER (from ASPENTECH) to obtain the values k(m) = 2.68 x 10(-7) m/s and A(v)k(o) = 0.0125 s(-1). Simulated results agreed satisfactorily well with experimental data. Consequently, the kinetic model and parameters were confirmed. Finally, a comparison between EPT and non-dispersive solvent extraction (NDSX) was carried out in order to evaluate the advantages and disadvantages of both membrane configurations. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:672 / 680
页数:9
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