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Original scientific paper

https://doi.org/10.15255/CABEQ.2017.1119

Optimization of Removal Efficiency and Minimum Contact Time for Cadmium and Zinc Removal onto Iron-modified Zeolite in a Two-stage Batch Sorption Reactor

M. Ugrina orcid id orcid.org/0000-0002-5042-2645 ; Faculty of Chemistry and Technology, University of Split, Ruđera Boškovića 35, 21000 Split, Croatia
N. Vukojević Medvidović orcid id orcid.org/0000-0002-8646-4249 ; Faculty of Chemistry and Technology, University of Split, Ruđera Boškovića 35, 21000 Split, Croatia
M. Trgo ; Faculty of Chemistry and Technology, University of Split, Ruđera Boškovića 35, 21000 Split, Croatia
I. Nuić orcid id orcid.org/0000-0002-8921-6224 ; Faculty of Chemistry and Technology, University of Split, Ruđera Boškovića 35, 21000 Split, Croatia


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Abstract

In highly congested industrial sites where significant volumes of effluents have to be treated in the minimum contact time, the application of a multi-stage batch reactor is suggested. To achieve better balance between capacity utilization and cost efficiency in
design optimization, a two-stage batch reactor is usually the optimal solution. Thus, in this paper, a two-stage batch sorption design approach was applied to the experimental data of cadmium and zinc uptake onto iron-modified zeolite. The optimization approach involves the application of the Vermeulen’s approximation model and mass balance equation to kinetic data. A design analysis method was developed to optimize the removal efficiency and minimum total contact time by combining the time required in the two-stages, in order to achieve the maximum percentage of cadmium and zinc removal using a fixed mass of zeolite. The benefits and limitations of the two-stage design approach have been investigated and discussed.







This work is licensed under a Creative Commons Attribution 4.0 International License.

Keywords

two-stage batch design; iron-modified zeolite; zinc; cadmium; optimization

Hrčak ID:

192269

URI

https://hrcak.srce.hr/192269

Publication date:

10.1.2018.

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