Jintao Xu, Ziyang Guo, Xiefei Zhu, Xiao Chen, Zejun Luo, Chunbao Charles Xu, Weihong Li
{"title":"Sequential catalysis enables efficient pyrolysis of food waste for syngas production","authors":"Jintao Xu, Ziyang Guo, Xiefei Zhu, Xiao Chen, Zejun Luo, Chunbao Charles Xu, Weihong Li","doi":"10.1016/j.biortech.2025.132042","DOIUrl":null,"url":null,"abstract":"Thermochemical conversion technologies are emerging as one of the most promising approaches to tackle food waste crisis. However, the existing techniques confront significant challenges in terms of syngas selectivity and catalyst stability. This study introduced a cost-effective Joule heating approach utilizing sequential catalysts composed of treated stainless steel (SS) and biochar to optimize syngas production from food waste. This system achieved a syngas yield of 17.64 mmol⋅g<ce:inf loc=\"post\">rice</ce:inf><ce:sup loc=\"post\">−1</ce:sup>, marking a 76.40 % improvement over conventional thermal pyrolysis. The molar ratio of hydrogen (H<ce:inf loc=\"post\">2</ce:inf>) to carbon monoxide (CO) was adjustable from 0.36 to 0.94, offering flexibility for different applications. Over five cycles, the system maintained robust catalytic stability, with only a 9.70 % decrease in syngas yield. Furthermore, the sequential catalysts proved versatile across diverse food wastes, achieving a maximum selectivity of 87.99 vol%. This approach enhanced catalyst activity and stability by promoting the sequential cracking of large oxygenates and reforming small molecules.","PeriodicalId":258,"journal":{"name":"Bioresource Technology","volume":"1 1","pages":""},"PeriodicalIF":9.7000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioresource Technology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1016/j.biortech.2025.132042","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURAL ENGINEERING","Score":null,"Total":0}
引用次数: 0
Abstract
Thermochemical conversion technologies are emerging as one of the most promising approaches to tackle food waste crisis. However, the existing techniques confront significant challenges in terms of syngas selectivity and catalyst stability. This study introduced a cost-effective Joule heating approach utilizing sequential catalysts composed of treated stainless steel (SS) and biochar to optimize syngas production from food waste. This system achieved a syngas yield of 17.64 mmol⋅grice−1, marking a 76.40 % improvement over conventional thermal pyrolysis. The molar ratio of hydrogen (H2) to carbon monoxide (CO) was adjustable from 0.36 to 0.94, offering flexibility for different applications. Over five cycles, the system maintained robust catalytic stability, with only a 9.70 % decrease in syngas yield. Furthermore, the sequential catalysts proved versatile across diverse food wastes, achieving a maximum selectivity of 87.99 vol%. This approach enhanced catalyst activity and stability by promoting the sequential cracking of large oxygenates and reforming small molecules.
期刊介绍:
Bioresource Technology publishes original articles, review articles, case studies, and short communications covering the fundamentals, applications, and management of bioresource technology. The journal seeks to advance and disseminate knowledge across various areas related to biomass, biological waste treatment, bioenergy, biotransformations, bioresource systems analysis, and associated conversion or production technologies.
Topics include:
• Biofuels: liquid and gaseous biofuels production, modeling and economics
• Bioprocesses and bioproducts: biocatalysis and fermentations
• Biomass and feedstocks utilization: bioconversion of agro-industrial residues
• Environmental protection: biological waste treatment
• Thermochemical conversion of biomass: combustion, pyrolysis, gasification, catalysis.