Tags

Type your tag names separated by a space and hit enter

Self-purification of actual wastewater via microbial-synergy driving of catalyst-surface microelectronic field: A pilot-scale study.
J Hazard Mater. 2023 Sep 05; 457:131744.JH

Abstract

High energy consumption is impedimental for eliminating refractory organics in wastewater by current technologies. Herein, we develop an efficient self-purification process for actual non-biodegradable dyeing wastewater at pilot scale, using N-doped graphene-like (CN) complexed Cu-Al2O3 supported Al2O3 ceramics (HCLL-S8-M) fixed-bed reactor without additional input. About 36% chemical oxygen demand removal was achieved within 20 min empty bed retention time and maintained stability for almost one year. The HCLL-S8-M structure feature and its interface on microbial community structure, functions, and metabolic pathways were analyzed by density-functional theory calculation, X-ray photoelectron spectroscopy, multiomics analysis of metagenome, macrotranscriptome and macroproteome. On the surface of HCLL-S8-M, a strong microelectronic field (MEF) was formed by the electron-rich/poor area due to Cu-π interaction from the complexation between phenolic hydroxy of CN and Cu species, driving the electrons of the adsorbed dye pollutants to the microorganisms through extracellular polymeric substance and the direct transfer of extracellular electrons, causing their degradation into CO2 and intermediates, which was degraded partly via intracellular metabolism. The lower energy feeding for the microbiome produced less adenosine triphosphate, resulting in little sludge throughout reaction. The MEF from electronic polarization is greatly potential to develop low-energy wastewater treatment technology.

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Xing X
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Lyu L
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Yan Z
Shandong Key Laboratory of Water pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Qingdao 266237, China.
Zhang H
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Li T
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Han M
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Li Z
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Zhang F
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Wang Z
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Wang S
Shandong Key Laboratory of Water pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Qingdao 266237, China.
Hong Y
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
Hu C
Institute of Environmental Research at Greater Bay, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China. Electronic address: huchun@gzhu.edu.cn.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

37285789

Citation

Xing, Xueci, et al. "Self-purification of Actual Wastewater Via Microbial-synergy Driving of Catalyst-surface Microelectronic Field: a Pilot-scale Study." Journal of Hazardous Materials, vol. 457, 2023, p. 131744.
Xing X, Lyu L, Yan Z, et al. Self-purification of actual wastewater via microbial-synergy driving of catalyst-surface microelectronic field: A pilot-scale study. J Hazard Mater. 2023;457:131744.
Xing, X., Lyu, L., Yan, Z., Zhang, H., Li, T., Han, M., Li, Z., Zhang, F., Wang, Z., Wang, S., Hong, Y., & Hu, C. (2023). Self-purification of actual wastewater via microbial-synergy driving of catalyst-surface microelectronic field: A pilot-scale study. Journal of Hazardous Materials, 457, 131744. https://doi.org/10.1016/j.jhazmat.2023.131744
Xing X, et al. Self-purification of Actual Wastewater Via Microbial-synergy Driving of Catalyst-surface Microelectronic Field: a Pilot-scale Study. J Hazard Mater. 2023 Sep 5;457:131744. PubMed PMID: 37285789.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Self-purification of actual wastewater via microbial-synergy driving of catalyst-surface microelectronic field: A pilot-scale study. AU - Xing,Xueci, AU - Lyu,Lai, AU - Yan,Zhen, AU - Zhang,Han, AU - Li,Tong, AU - Han,Muen, AU - Li,Zesong, AU - Zhang,Fagen, AU - Wang,Zhu, AU - Wang,Shuguang, AU - Hong,Yiguo, AU - Hu,Chun, Y1 - 2023/05/30/ PY - 2023/02/10/received PY - 2023/05/12/revised PY - 2023/05/29/accepted PY - 2023/6/8/medline PY - 2023/6/8/pubmed PY - 2023/6/7/entrez KW - Dyeing wastewater KW - Electroactive microorganisms KW - Extracellular electron transfer KW - HCLL-S8-M KW - Surface microelectronic field SP - 131744 EP - 131744 JF - Journal of hazardous materials JO - J Hazard Mater VL - 457 N2 - High energy consumption is impedimental for eliminating refractory organics in wastewater by current technologies. Herein, we develop an efficient self-purification process for actual non-biodegradable dyeing wastewater at pilot scale, using N-doped graphene-like (CN) complexed Cu-Al2O3 supported Al2O3 ceramics (HCLL-S8-M) fixed-bed reactor without additional input. About 36% chemical oxygen demand removal was achieved within 20 min empty bed retention time and maintained stability for almost one year. The HCLL-S8-M structure feature and its interface on microbial community structure, functions, and metabolic pathways were analyzed by density-functional theory calculation, X-ray photoelectron spectroscopy, multiomics analysis of metagenome, macrotranscriptome and macroproteome. On the surface of HCLL-S8-M, a strong microelectronic field (MEF) was formed by the electron-rich/poor area due to Cu-π interaction from the complexation between phenolic hydroxy of CN and Cu species, driving the electrons of the adsorbed dye pollutants to the microorganisms through extracellular polymeric substance and the direct transfer of extracellular electrons, causing their degradation into CO2 and intermediates, which was degraded partly via intracellular metabolism. The lower energy feeding for the microbiome produced less adenosine triphosphate, resulting in little sludge throughout reaction. The MEF from electronic polarization is greatly potential to develop low-energy wastewater treatment technology. SN - 1873-3336 UR - https://www.unboundmedicine.com/medline/citation/37285789/Self_purification_of_actual_wastewater_via_microbial_synergy_driving_of_catalyst_surface_microelectronic_field:_A_pilot_scale_study_ DB - PRIME DP - Unbound Medicine ER -