金若菲

个人信息Personal Information

副教授

硕士生导师

主要任职:环境学院副院长

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:环境学院

学科:环境工程

办公地点:环境楼B711

联系方式:jruofei@dlut.edu.cn

电子邮箱:jruofei@dlut.edu.cn

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Facilitated bioreduction of nitrobenzene by lignite acting as low-cost and efficient electron shuttle

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论文类型:期刊论文

发表时间:2020-06-01

发表刊物:CHEMOSPHERE

收录刊物:PubMed、EI、SCIE

卷号:248

页面范围:125978

ISSN号:0045-6535

关键字:Lignite; Nitrobenzene bioreduction; Shewanella oneidensis; Redox mediator; Nitric acid treatment

摘要:The searching for efficient and economical redox mediators to promote the treatment of wastewater containing recalcitrant organic compounds is greatly needed. In this study, the redox mediator activities of four different lignite samples to facilitate the bioreduction of nitrobenzene by Shewanella oneidensis MR-1 were tested for the first time. The initial nitrobenzene reduction rate was increased by 40.4%-90.3% in the presence of 50 mg/L of different lignite samples. Lignite collected from Xinjiang (XJL) having more oxygenated groups performed better in enhancing nitrobenzene bioreduction. The stimulating effects increased with the increase of lignite dosage (0-200 mg/L) and the decrease of lignite particle size (150-0.1 mu m). However, the pristine XJL samples with assorted sizes of particles exhibited better stimulating effects than size-fractionated ones, implying that different-sized XJL particles might have synergetic effects on the bioreduction process. When humic acid or iron was removed from XJL, its promoting effects were decreased, demonstrating the crucial roles of both components in lignite-enhanced nitrobenzene bioreduction. Nitric acid treatment could form more oxygenated moieties on lignite surface, which played vital roles in promoting nitrobenzene bioreduction. The initial nitrobenzene bioreduction rate in the presence of HNO3-treated XJL was 80.8% higher than that obtained with pristine XJL. This study proposed an effective and readily available redox mediator that could be applied to promote the bioreduction of recalcitrant electrophilic pollutants. (C) 2020 Elsevier Ltd. All rights reserved.