Desulfurization: Critical step towards enhanced selenium removal from industrial effluents

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TitreDesulfurization: Critical step towards enhanced selenium removal from industrial effluents
Type de publicationJournal Article
Year of Publication2017
AuteursStaicu LC, Morin-Crini N, Crini G
JournalCHEMOSPHERE
Volume172
Pagination111-119
Date PublishedAPR
Type of ArticleArticle
ISSN0045-6535
Mots-clésadsorption, Desulfurization, FerrIX A33E resin, FGD wastewater, Selenium pollution
Résumé

Selenium (Se) removal from synthetic solutions and from real Flue Gas Desulfurization (FGD) wastewater generated by a coal-fired power plant was studied for the first time using a commercial iron oxide impregnated strong base anion exchange resin, Purolite (R) FerrIX A33E. In synthetic solutions, the resin showed high affinity for selenate and selenite, while sulfate exhibited a strong competition for both oxyanions. The FGD wastewater investigated is a complex system that contains Se (similar to 1200 mu g L-1), SO (similar to 1.1 g L-1), Cl- (similar to 9.5 g L-1), and Ca2+ (similar to 5 g L-1), alongside a broad spectrum of toxic trace metals including Cd, Cr, Hg, Ni, and Zn. The resin performed poorly against Se in the raw FGD wastewater and showed moderate to good removal of several trace elements such as Cd, Cr, Hg, and Zn. In FGD effluent, sulfate was identified as a powerful competing anion for Se, having high affinity for the exchange active sites of the resin. The desulfurization of the FGD effluent using BaCl2 led to the increase in Se removal from 3% (non-desulfurized effluent) to 80% (desulfurized effluent) by combined precipitation and ion exchange treatment. However, complete desulfurization using equimolar BaCl2 could not be achieved due to the presence of bicarbonate that acts as a sulfate competitor for barium. In addition to selenium and sulfate removal, several toxic metals were efficiently removed (Cd: 91%; Cr: 100%; Zn: 99%) by the combined (desulfurization and ion exchange) treatment. (C) 2016 Elsevier Ltd. All rights reserved.

DOI10.1016/j.chemosphere.2016.12.132