污泥源生物炭促进热碱性预处理污泥厌氧消化产甲烷:性能与机理

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yin-Ping Hou , Fang-Yuan Wang , Wang-Tao Dong , Hong-Rui Ma , Bin-Bin Cai
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引用次数: 0

摘要

在厌氧消化(AD)中添加生物炭是一种很有前途的通过加强直接种间电子转移(DIET)来提高硫酸铵产量的策略。本研究考察了在300/500/700℃条件下制备的三种污泥源生物炭(分别命名为BC300、BC500和BC700)在热碱预处理的废活性污泥(WAS) AD过程中提高硫酸铵生产效率和系统稳定性的效果。对照、BC300、BC500和BC700组的最大硫酸铵产量分别为326.8 mL/g VS、401.8 mL/g VS、423.8 mL/g VS和420 mL/g VS。与BC300和BC700相比,BC500对硫酸铵的最大产量提高了35.4% %。电化学分析表明,BC500同时具有表面氧化还原官能团和石墨结构,使其具有优良的电容(0.31 mF/g)和电导率(3.1 ×10−4 S/m),有利于DIET。微生物群落分析表明,在生物炭添加组中,能够参与DIET的乙营养化产甲烷菌Methanosaeta的丰度从24.0 %增加到32.3-34.0 %。这些发现表明,在was AD期间,DIET被优先刺激以促进甲烷生成,取代了热力学上不利的氢介导的种间电子转移。本研究为污泥源生物炭原位强化AD提供了理论基础,并提出了一种闭环“以废治废”策略:提高WAS的能量回收和污水处理厂(WWTPs)的可持续污泥管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sludge-derived biochar promoted the methane production in anaerobic digestion of thermo-alkaline pretreated waste-activated sludge: Performance and mechanisms
The addition of biochar is a promising strategy to improve CH₄ production by strengthening direct interspecies electron transfer (DIET) in anaerobic digestion (AD). In this study, three types of sludge-derived biochar prepared at 300/500/700 °C (designated BC300, BC500, and BC700) were evaluated for their effects in improving CH₄ production efficiency and system stability during AD of thermo-alkaline pretreated waste-activated sludge (WAS). The maximum CH₄ production for the control, BC300, BC500, and BC700 groups was 326.8 mL/g VS, 401.8 mL/g VS, 423.8 mL/g VS, and 420 mL/g VS, respectively. BC500 promoted more significantly than BC300 and BC700, with 35.4 % higher maximum CH₄ production than the control group. Electrochemical analysis demonstrated that BC500 possesses both surface redox functional groups and graphitic structure, endowing it with excellent capacitance (0.31 mF/g) and electrical conductivity (3.1 ×10−4 S/m), which facilitates DIET. Microbial community analysis revealed that the acetotrophic methanogens Methanosaeta, which are capable of participating in DIET, were enriched from 24.0 % to 32.3–34.0 % in the biochar-added groups. These findings suggest that DIET was preferentially stimulated to promote methanogenesis during WAS AD, replacing the thermodynamically unfavorable hydrogen-mediated interspecies electron transfer. This study provides a theoretical foundation for in-situ enhanced AD via sludge-derived biochar and proposes a closed-loop “treating waste with waste” strategy: improved energy recovery from WAS and sustainable sludge management in wastewater treatment plants (WWTPs).
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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