4.7 Article

Biodegradation of organophosphorus pesticides in moving bed biofilm reactors: Analysis of microbial community and biodegradation pathways

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JOURNAL OF HAZARDOUS MATERIALS
卷 408, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.jhazmat.2020.124950

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Organophosphorus pesticides; Moving bed biofilm reactors; Micropollutants removal; Biofilms

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The performance of a lab-scale moving bed biofilm reactor for general bioconversion processes and biotransformation of organophosphorus pesticides was investigated. Decrease in organic load resulted in thinner biofilm and more biomass, shifting bioconversion processes. The reactor supported more nitrification at low organic loading, but denitrification was enhanced at higher organic loading.
We investigated the performance of a lab-scale moving bed biofilm reactor (MBBR) with respect to general bioconversion processes and biotransformation of two commonly used organophosphorus pesticides, Chlorpyrifos (CHL) and Malathion (MAL). The reactor was operated for 300 days under different organic loads by changing hydraulic retention time (HRT). The decrease in organic load resulted in the formation of a thinner biofilm and the growth of more biomass in the bulk, which greatly shifted bioconversion processes. The low organic loading supported more nitrification in the reactor, but an opposite trend was observed for denitrification, which was enhanced at higher organic loading where the formation of anoxic zones in the thick biofilm was favored. 70% and 55% removal corresponding to 210 and 165 mu g/m(2)/d occurred for MAL and CHL, respectively, at an HRT of 3 h and progressively increased with higher HRTs. Phylogenetic analysis revealed a shift in composition and abundance of taxa throughout the reactor operation where lower loading rate supported the growth of a more diverse and evenly distributed community. The analysis also highlighted the dominance of heterotrophic communities such as Flavobacterium and Acinetobacter johnsonii, which could be involved in the biotransformation of CHL and MAL through co-metabolism.

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