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通过钴催化热解和产甲烷共消化从废水藻类生物质中生产沼气的化学机制

Chemical mechanisms of biogas production from wastewater algal biomass via cobalt-catalysed pyrolysis and methanogenic co-digestion.

作者信息

Zuo Ning, He JinChao, Tan XueMei

机构信息

Southwest Research Institute for Hydraulic and Water Transport Engineering, Chongqing Jiaotong University, Chongqing, China.

Key Laboratory of Inland Waterway Regulation Technology Transportation Industry, Chongqing, China.

出版信息

PLoS One. 2025 May 6;20(5):e0321364. doi: 10.1371/journal.pone.0321364. eCollection 2025.

DOI:10.1371/journal.pone.0321364
PMID:40327643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12054884/
Abstract

Biogas energy derived from recycled algal biomass grown on wastewater could provide a sustainable pathway for a renewable future. This research investigates the chemical details of cobalt-catalysed pyrolysis integrated with methanogenic archaea co-anaerobic fermentation to improve biogas and methane generation from wastewater algae. Algal biomass (500 mL sample) was harvested from multiple locations at the Qinghe Wastewater Treatment Plant in Beijing, China. The algal species Chlorella vulgaris and Scenedesmus obliquus were identified. A 5% Co/Al₂O₃ catalyst was prepared by impregnating commercial alumina with a cobalt nitrate solution. Pyrolysis was conducted in a 500 mL fixed-bed reactor, and bio-oil and char yields were measured. Thermal degradation of biomass and by-products was analysed using thermogravimetric analysis (TGA). Microbial cultures of Methanosaeta concilii and Methanosarcina barkeri were used for anaerobic fermentation in 1 L batch biodigesters, with bio-oil as the carbon source. Biogas production kinetics were modelled using the modified Gompertz and Arrhenius equations. Statistical analyses were performed using GraphPad Prism version 10.2.0 and R version 4.03. The results demonstrated that biogas production in the experimental group was significantly higher across all temperatures. Maximum methane yield (Pmax) increased from 301.05 mL at 400°C to 436.71 mL at 800°C in the experimental group, compared to the control group. The rate constant (k) for biogas production also increased, reaching 0.20 mL/day at 800°C in the experimental group. CO₂ yield was higher in the control group at lower temperatures, while the integrated system consistently produced more biochar and biogas. The energy efficiency analysis revealed that the calorific value of biogas increased from 7.552 MJ at 400°C to 12.966 MJ at 800°C in the experimental group, with net energy gain decreasing as temperature increased. The mass balance showed that, during the pyrolysis stage, 100 g of biomass resulted in 35 g of biochar, 250 mL of biogas, and 50 g of bio-oil. In the anaerobic digestion stage, 155.47 g of biochar and 300 mL of biogas were produced. Kinetic model analysis showed that the activation energy for pyrolysis in the experimental group decreased from 145 kJ/mol at 400°C to 125 kJ/mol at 800°C, while the maximum methane yield in the Gompertz model increased from 405.026 mL at 400°C to 434.525 mL at 800°C in the experimental group. Thermogravimetric analysis (TGA) showed that biomass had 96.8% volatile matter, while biochar had 87.5% volatile matter and 12.5% ash content. BET surface area analysis of Co/Al₂O₃ biochar showed a surface area of 400 m²/g. Cobalt-catalysed pyrolysis and the subsequent anaerobic digestion process provide synergistic effects, leading to enhanced biogas yield while reducing the production time required.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/5c48466a0667/pone.0321364.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/675fb1a3228f/pone.0321364.g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/066154f5cf41/pone.0321364.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/cc8983df8724/pone.0321364.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/947cd3eb7257/pone.0321364.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/ad89ca0509d2/pone.0321364.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/5c48466a0667/pone.0321364.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/675fb1a3228f/pone.0321364.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/218b6c0d6f9b/pone.0321364.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/03284ba3f3ba/pone.0321364.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/066154f5cf41/pone.0321364.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/cc8983df8724/pone.0321364.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/947cd3eb7257/pone.0321364.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/ad89ca0509d2/pone.0321364.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700a/12054884/5c48466a0667/pone.0321364.g008.jpg
摘要

源自废水培养的循环利用藻类生物质的沼气能源可为可再生未来提供一条可持续途径。本研究调查了钴催化热解与产甲烷古菌共厌氧发酵相结合的化学细节,以提高废水藻类产生的沼气和甲烷产量。从中国北京清河污水处理厂的多个地点采集了藻类生物质(500毫升样品)。鉴定出小球藻和斜生栅藻这两种藻类。通过用硝酸钴溶液浸渍商业氧化铝制备了5%的Co/Al₂O₃催化剂。在500毫升固定床反应器中进行热解,并测量生物油和焦炭产量。使用热重分析(TGA)分析生物质和副产物的热降解。以Methanosaeta concilii和Methanosarcina barkeri的微生物培养物作为碳源,在1升分批生物消化器中进行厌氧发酵。使用修正的Gompertz方程和Arrhenius方程对沼气生产动力学进行建模。使用GraphPad Prism 10.2.0版和R 4.03版进行统计分析。结果表明,在所有温度下,实验组的沼气产量均显著更高。与对照组相比,实验组的最大甲烷产量(Pmax)从400°C时的301.05毫升增加到800°C时的436.71毫升。实验组沼气生产的速率常数(k)也增加,在800°C时达到0.20毫升/天。在较低温度下,对照组的CO₂产量较高,而集成系统始终产生更多的生物炭和沼气。能量效率分析表明,实验组中沼气的热值从400°C时的7.552兆焦增加到800°C时的12.966兆焦,净能量增益随温度升高而降低。质量平衡表明,在热解阶段,100克生物质产生35克生物炭、250毫升沼气和50克生物油。在厌氧消化阶段,产生了155.47克生物炭和300毫升沼气。动力学模型分析表明,实验组热解的活化能从400°C时的145千焦/摩尔降至800°C时的1

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