{"title":"生物质-甲烷共热解生产富氢合成气:热力学分析。","authors":"Haiyan Guo, Zhiling Wang, Kang Kang, Dongbing Li","doi":"10.3390/polym17192695","DOIUrl":null,"url":null,"abstract":"<p><p>This study presents a thermodynamic equilibrium analysis of hydrogen-rich syngas production via biomass-methane co-pyrolysis, employing the Gibbs free energy minimization method. A critical temperature threshold at 700 °C is identified, below which methanation and carbon deposition are thermodynamically favored, and above which cracking and reforming reactions dominate, enabling high-purity syngas generation. Methane addition shifts the reaction pathway towards increased reduction, significantly enhancing carbon and H<sub>2</sub> yields while limiting CO and CO<sub>2</sub> emissions. At 1200 °C and a 1:1 methane-to-biomass ratio, cellulose produces 50.84 mol C/kg, 119.69 mol H<sub>2</sub>/kg, and 30.65 mol CO/kg; lignin yields 78.16 mol C/kg, 117.69 mol H<sub>2</sub>/kg, and 19.14 mol CO/kg. The H<sub>2</sub>/CO ratio rises to 3.90 for cellulose and 6.15 for lignin, with energy contents reaching 43.16 MJ/kg and 52.91 MJ/kg, respectively. Notably, biomass enhances methane conversion from 25% to over 53% while sustaining a 67% H<sub>2</sub> selectivity. These findings demonstrate that syngas composition and energy content can be precisely controlled via methane co-feeding ratio and temperature, offering a promising approach for sustainable, tunable syngas production.</p>","PeriodicalId":20416,"journal":{"name":"Polymers","volume":"17 19","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2025-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12526537/pdf/","citationCount":"0","resultStr":"{\"title\":\"Production of Hydrogen-Rich Syngas via Biomass-Methane Co-Pyrolysis: Thermodynamic Analysis.\",\"authors\":\"Haiyan Guo, Zhiling Wang, Kang Kang, Dongbing Li\",\"doi\":\"10.3390/polym17192695\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This study presents a thermodynamic equilibrium analysis of hydrogen-rich syngas production via biomass-methane co-pyrolysis, employing the Gibbs free energy minimization method. A critical temperature threshold at 700 °C is identified, below which methanation and carbon deposition are thermodynamically favored, and above which cracking and reforming reactions dominate, enabling high-purity syngas generation. Methane addition shifts the reaction pathway towards increased reduction, significantly enhancing carbon and H<sub>2</sub> yields while limiting CO and CO<sub>2</sub> emissions. At 1200 °C and a 1:1 methane-to-biomass ratio, cellulose produces 50.84 mol C/kg, 119.69 mol H<sub>2</sub>/kg, and 30.65 mol CO/kg; lignin yields 78.16 mol C/kg, 117.69 mol H<sub>2</sub>/kg, and 19.14 mol CO/kg. The H<sub>2</sub>/CO ratio rises to 3.90 for cellulose and 6.15 for lignin, with energy contents reaching 43.16 MJ/kg and 52.91 MJ/kg, respectively. Notably, biomass enhances methane conversion from 25% to over 53% while sustaining a 67% H<sub>2</sub> selectivity. These findings demonstrate that syngas composition and energy content can be precisely controlled via methane co-feeding ratio and temperature, offering a promising approach for sustainable, tunable syngas production.</p>\",\"PeriodicalId\":20416,\"journal\":{\"name\":\"Polymers\",\"volume\":\"17 19\",\"pages\":\"\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-10-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12526537/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymers\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.3390/polym17192695\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymers","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.3390/polym17192695","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Production of Hydrogen-Rich Syngas via Biomass-Methane Co-Pyrolysis: Thermodynamic Analysis.
This study presents a thermodynamic equilibrium analysis of hydrogen-rich syngas production via biomass-methane co-pyrolysis, employing the Gibbs free energy minimization method. A critical temperature threshold at 700 °C is identified, below which methanation and carbon deposition are thermodynamically favored, and above which cracking and reforming reactions dominate, enabling high-purity syngas generation. Methane addition shifts the reaction pathway towards increased reduction, significantly enhancing carbon and H2 yields while limiting CO and CO2 emissions. At 1200 °C and a 1:1 methane-to-biomass ratio, cellulose produces 50.84 mol C/kg, 119.69 mol H2/kg, and 30.65 mol CO/kg; lignin yields 78.16 mol C/kg, 117.69 mol H2/kg, and 19.14 mol CO/kg. The H2/CO ratio rises to 3.90 for cellulose and 6.15 for lignin, with energy contents reaching 43.16 MJ/kg and 52.91 MJ/kg, respectively. Notably, biomass enhances methane conversion from 25% to over 53% while sustaining a 67% H2 selectivity. These findings demonstrate that syngas composition and energy content can be precisely controlled via methane co-feeding ratio and temperature, offering a promising approach for sustainable, tunable syngas production.
期刊介绍:
Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.