4.8 Article

Enhancing sludge methanogenesis with improved redox activity of extracellular polymeric substances by hematite in red mud

期刊

WATER RESEARCH
卷 134, 期 -, 页码 54-62

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2018.01.062

关键词

Conductive materials; Extracellular polymeric substances (EPS); Interspecies electron transfer; Aggregates; Redox activity

资金

  1. National Natural Science Foundation of China [51608121, 41671264, 41601241]
  2. Project of Fujian Provincial Department of Science and Technology, China [2016N5004, 2017N0007]
  3. Project of Fujian Development and Reform Commission, China [20160527]

向作者/读者索取更多资源

Different conductive materials have been employed to stimulate direct interspecies electron transfer (DIET) during methanogenesis, but few studies have been concerned with the interaction between conductive materials and extracellular polymeric substances (EPS) such as the effect on sludge aggregation and redox activity of EPS. This study aims to systematically investigate the role of red mud with 45.46 wt% hematite on methanogenesis during the anaerobic digestion of waste activated sludge. The results showed that the multivalent cations from hematite effectively promoted the formation of large and compact aggregates, which might contribute to the rapid direct electron exchange during the DIET process. Meanwhile,, more redox-active mediators, including c-type cytochromes (c-Cyts) and humic substances, particularly in tight-bound EPS (TB-EPS), and more redox-active metals such as Fe introduced by red mud could take part in the interspecies electron transfer process between syntrophic bacteria and methanogenic archaea, which also promoted methane production (35.52 +/- 2.64% increase compared with the control). This study provided initial scientific evidence to comprehensively assess the role of conductive materials during methanogenesis, with important implications for the biogeochemical redox processes of conductive minerals in natural and engineered environments. (C) 2018 Elsevier Ltd. All rights reserved.

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