File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Quaternary Ammonium Compound in Anolyte without Functionalization Accelerates the Startup of Bioelectrochemical Systems using Real Wastewater

TitleQuaternary Ammonium Compound in Anolyte without Functionalization Accelerates the Startup of Bioelectrochemical Systems using Real Wastewater
Authors
KeywordsBioelectrochemical systems
Microbial community
Microbial fuel cells
Quaternary ammonium compounds
Startup
Issue Date2016
Citation
Electrochimica Acta, 2016, v. 188, p. 801-808 How to Cite?
AbstractQuaternary ammonium has been demonstrated to be an efficient functional group for anodic material modification in bioelectrochemical systems (BESs). However, not all anode materials can be easily functionalized with quaternary ammonium. Here QAC of 0.05 M, 0.01 M and 0.001 M is directly added in anolyte instead of complex material functionalization. The startup time of 0.01 M (91 ± 0.5 h) and 0.001 M (101 ± 1 h) using real wastewater were 29% and 21% shorter than 128 ± 1.5 h of the no QAC control. Coulombic efficiency increased by 95% from 37 ± 1% (control) to 72 ± 2% (0.01 M), while the startup was obviously inhibited up to 0.05 M due to its biotoxicity. Cyclic voltammetry reveals that 0.01 M had a 23% higher peak current density than the control with a broader redox window observed. High-throughput sequencing confirmed that QAC imposed a selective stress on anodic microbial community. This provides a simple method to accelerate BES startup for anodes that not be easily modified.
Persistent Identifierhttp://hdl.handle.net/10722/352936
ISSN
2023 Impact Factor: 5.5
2023 SCImago Journal Rankings: 1.159
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorFeng, Cuijuan-
dc.contributor.authorLiu, Yinan-
dc.contributor.authorLi, Qiang-
dc.contributor.authorChe, You-
dc.contributor.authorLi, Nan-
dc.contributor.authorWang, Xin-
dc.date.accessioned2025-01-13T03:01:09Z-
dc.date.available2025-01-13T03:01:09Z-
dc.date.issued2016-
dc.identifier.citationElectrochimica Acta, 2016, v. 188, p. 801-808-
dc.identifier.issn0013-4686-
dc.identifier.urihttp://hdl.handle.net/10722/352936-
dc.description.abstractQuaternary ammonium has been demonstrated to be an efficient functional group for anodic material modification in bioelectrochemical systems (BESs). However, not all anode materials can be easily functionalized with quaternary ammonium. Here QAC of 0.05 M, 0.01 M and 0.001 M is directly added in anolyte instead of complex material functionalization. The startup time of 0.01 M (91 ± 0.5 h) and 0.001 M (101 ± 1 h) using real wastewater were 29% and 21% shorter than 128 ± 1.5 h of the no QAC control. Coulombic efficiency increased by 95% from 37 ± 1% (control) to 72 ± 2% (0.01 M), while the startup was obviously inhibited up to 0.05 M due to its biotoxicity. Cyclic voltammetry reveals that 0.01 M had a 23% higher peak current density than the control with a broader redox window observed. High-throughput sequencing confirmed that QAC imposed a selective stress on anodic microbial community. This provides a simple method to accelerate BES startup for anodes that not be easily modified.-
dc.languageeng-
dc.relation.ispartofElectrochimica Acta-
dc.subjectBioelectrochemical systems-
dc.subjectMicrobial community-
dc.subjectMicrobial fuel cells-
dc.subjectQuaternary ammonium compounds-
dc.subjectStartup-
dc.titleQuaternary Ammonium Compound in Anolyte without Functionalization Accelerates the Startup of Bioelectrochemical Systems using Real Wastewater-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.electacta.2015.12.069-
dc.identifier.scopuseid_2-s2.0-84950264509-
dc.identifier.volume188-
dc.identifier.spage801-
dc.identifier.epage808-
dc.identifier.isiWOS:000370986500094-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats