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Metal oxyanion removal from wastewater using manganese-oxidizing aerobic granular sludge.

Authors :
He, Zhanfei
Wei, Zhen
Zhang, Qingying
Zou, Jinte
Pan, Xiangliang
Source :
Chemosphere. Dec2019, Vol. 236, pN.PAG-N.PAG. 1p.
Publication Year :
2019

Abstract

As, Sb, and Cr are redox-sensitive and toxic heavy metal(loid)s, and redox reactions are usually involved in the treatment of substrates containing these elements. In this study, manganese-oxidizing aerobic granular sludge (Mn-AGS) was obtained by continuously adding Mn(II) to the sludge in a sequencing batch reactor (SBR). Morphological observations, and analyses of extracellular polymeric substances (EPS), Mn valence-states, and microbial communities were performed on the resulting sludge. After 50 days of cultivation, biogenic Mn(III,IV) oxides (bio-MnO x) accumulated up to approximately 25 mg Mn/g suspended solids (SS). X-ray photoelectron spectroscopy (XPS) revealed that the percentage of Mn(III,IV) was 87.6%. The protein (PN) component in EPS increased from 80.3 to 87.8 mg/g volatile suspended solids (VSS) during cultivation, which might be favorable for sludge granulation and heavy metal(loid) removal. Batch experiments showed that Mn-AGS was better at oxidizing As(III)/Sb(III) into less toxic As(V)/Sb(V) than traditional AGS. Remarkably, the results indicated that Mn-AGS did not oxidize Cr(III) but was able to reduce Cr(VI) into relatively harmless Cr(III). This work provided a new promising method with which to treat As(III), Sb(III), and Cr(VI) in wastewaters. Image 1 • Manganese-oxidizing aerobic granular sludge (Mn-AGS) was successfully obtained. • A high level of biogenic MnO x accumulation was observed in aerobic granules. • Oxidation of As(III)/Sb(III) into less toxic forms was largely improved by Mn-AGS. • Cr(III) was not oxidized but Cr(VI) was reduced into harmless Cr(III) by Mn-AGS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
236
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
138984152
Full Text :
https://doi.org/10.1016/j.chemosphere.2019.124353