矿化(土壤科学)
光催化
生物降解
化学
生物转化
生物膜
环境化学
催化作用
有机化学
细菌
生物
酶
遗传学
氮气
作者
Houfeng Xiong,Shuangshi Dong,Jun Zhang,Dandan Zhou,Bruce E. Rittmann
出处
期刊:Water Research
[Elsevier BV]
日期:2018-03-02
卷期号:136: 75-83
被引量:149
标识
DOI:10.1016/j.watres.2018.02.061
摘要
Intimately coupled photocatalysis and biodegradation (ICPB) was realized in a macroporous carrier in which a photocatalyst was present on the outer surface, while a biofilm accumulated inside the carrier. In ICPB, photocatalysis products are rapidly biodegraded by a protected biofilm, leading to mineralization of the refractory organics, such as antibiotics. However, mineralization in ICPB could be compromised if the photocatalysis products remain refractory or are inhibitory. To address this, we attempted to increase metabolic activity by providing a readily biodegradable co-substrate (acetate) that could act as a source of energy and electrons to improve biotransformation and mineralization of the refractory antibiotic tetracycline (TCH). When we added acetate during ICPB of TCH, TCH removal increased by ∼5%, mineralization increased by ∼20%, and almost all photocatalysis products disappeared. Acetate addition also led to an increase in active biomass, an increase in the biomass's respiratory activity, and evolution of the microbial community to having more members able to biodegrade photocatalysis and biotransformation intermediates. Thus, providing an easily biodegradable co-substrate was an effective means for enhancing TCH removal and mineralization with the ICPB technology.
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