Biochar based removal of antibiotic sulfonamides and tetracyclines in aquatic environments: A critical review

[Display omitted] •Limited knowledge is present on surface interactions of biochar on antibiotics.•Remediation is governed by properties of biochar as well as antibiotics.•Presence of other ions, DOC, and pH influence antibiotics removal.•Predominant adsorption mechanism is electron donor accepter i...

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Published inBioresource technology Vol. 246; pp. 150 - 159
Main Authors Peiris, Chathuri, Gunatilake, Sameera R., Mlsna, Todd E., Mohan, Dinesh, Vithanage, Meththika
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.12.2017
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Summary:[Display omitted] •Limited knowledge is present on surface interactions of biochar on antibiotics.•Remediation is governed by properties of biochar as well as antibiotics.•Presence of other ions, DOC, and pH influence antibiotics removal.•Predominant adsorption mechanism is electron donor accepter interaction. Utilization of biochar (BC) as a low cost adsorbent for water remediation has gained an immense research interest due to their surface functionality and porosity. Although many reports on the BC based sorptive removal of Sulfonamides (SA) and Tetracyclines (TC) are available in literature, a deep insight into sorption mechanisms is yet to be reviewed. Objective of this review is to fill the research gap of a methodological understanding of sorption mechanisms and characteristics which is essential to develop efficient methods for contaminant removal. The most common adsorption mechanism can be considered as electron donor-acceptor interactions of electron withdrawing moieties with surface arene rings. The strongest adsorption of both antibiotics occurs at mildly acidic pH where the dominant species are zwitterionic or cationic. Smaller SAs exhibit micro pore-filling effects while bulky TCs experience size exclusions. Furthermore, the effect of matrix components and modifications are also been taken into account.
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ISSN:0960-8524
1873-2976
1873-2976
DOI:10.1016/j.biortech.2017.07.150