Jiaqi Deng , Baojun Yi , Ondřej Mašek , Xiangzhou Yuan , Sung Yeon Hwang , Hwai Chyuan Ong , Zewen Hua , Yong Sik Ok
{"title":"生物质和塑料废物共热解成碳材料与环境应用:一个关键的审查†","authors":"Jiaqi Deng , Baojun Yi , Ondřej Mašek , Xiangzhou Yuan , Sung Yeon Hwang , Hwai Chyuan Ong , Zewen Hua , Yong Sik Ok","doi":"10.1039/d4gc04842c","DOIUrl":null,"url":null,"abstract":"<div><div>The urgent need for global energy transformation and environmental protection, combined with widespread plastic contamination, has stimulated research into the co-pyrolysis of biomass and plastic waste. This approach challenges traditional resource utilization methods and opens new pathways for sustainable energy generation and waste management. The reaction processes and mechanisms of both biomass pyrolysis and various plastic wastes are comprehensively examined. The influences of co-processing parameters on the composition, content, and product characteristics are analysed, providing a solid theoretical foundation for the large-scale production and application of co-pyrolysis. Besides the potential problems related to plastic co-pyrolysis, the enhancement of carbon materials’ properties by plastic waste in co-pyrolysis is also explored, which is significant for the functionalization of carbon materials. The reaction mechanism, reaction process, reaction conditions, and products generated from the co-pyrolysis of biomass and plastic waste are discussed. In the co-pyrolysis of biomass (especially lignocellulosic biomass) and plastic waste, PET, PU, and PVC are more conducive to the production of carbon materials, while PP, PE, and PS are more favourable for the generation of bio-oils. The interaction between the hydroxyl radicals provided by biomass and the hydrogen radicals provided by plastic waste enhances the reaction. Slow co-pyrolysis at 500 °C, a feedstock ratio of 3 : 1 (biomass to plastic waste), and a suitable catalyst (such as zeolites) are more beneficial for carbon materials in terms of the yield, porosity, and production rate. Co-pyrolysis carbon materials possess superior hydrophobicity and adsorption properties compared to conventional carbon materials and can be enriched in elements often absent from the original carbon materials, such as nitrogen. These potential advantages of co-pyrolyzing plastics with biomass open new prospects beyond waste management, such as enhanced material development for a range of environmental and agricultural applications.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 22","pages":"Pages 6320-6341"},"PeriodicalIF":9.2000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Co-pyrolysis of biomass and plastic waste into carbon materials with environmental applications: a critical review†\",\"authors\":\"Jiaqi Deng , Baojun Yi , Ondřej Mašek , Xiangzhou Yuan , Sung Yeon Hwang , Hwai Chyuan Ong , Zewen Hua , Yong Sik Ok\",\"doi\":\"10.1039/d4gc04842c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The urgent need for global energy transformation and environmental protection, combined with widespread plastic contamination, has stimulated research into the co-pyrolysis of biomass and plastic waste. This approach challenges traditional resource utilization methods and opens new pathways for sustainable energy generation and waste management. The reaction processes and mechanisms of both biomass pyrolysis and various plastic wastes are comprehensively examined. The influences of co-processing parameters on the composition, content, and product characteristics are analysed, providing a solid theoretical foundation for the large-scale production and application of co-pyrolysis. Besides the potential problems related to plastic co-pyrolysis, the enhancement of carbon materials’ properties by plastic waste in co-pyrolysis is also explored, which is significant for the functionalization of carbon materials. The reaction mechanism, reaction process, reaction conditions, and products generated from the co-pyrolysis of biomass and plastic waste are discussed. In the co-pyrolysis of biomass (especially lignocellulosic biomass) and plastic waste, PET, PU, and PVC are more conducive to the production of carbon materials, while PP, PE, and PS are more favourable for the generation of bio-oils. The interaction between the hydroxyl radicals provided by biomass and the hydrogen radicals provided by plastic waste enhances the reaction. Slow co-pyrolysis at 500 °C, a feedstock ratio of 3 : 1 (biomass to plastic waste), and a suitable catalyst (such as zeolites) are more beneficial for carbon materials in terms of the yield, porosity, and production rate. Co-pyrolysis carbon materials possess superior hydrophobicity and adsorption properties compared to conventional carbon materials and can be enriched in elements often absent from the original carbon materials, such as nitrogen. 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Co-pyrolysis of biomass and plastic waste into carbon materials with environmental applications: a critical review†
The urgent need for global energy transformation and environmental protection, combined with widespread plastic contamination, has stimulated research into the co-pyrolysis of biomass and plastic waste. This approach challenges traditional resource utilization methods and opens new pathways for sustainable energy generation and waste management. The reaction processes and mechanisms of both biomass pyrolysis and various plastic wastes are comprehensively examined. The influences of co-processing parameters on the composition, content, and product characteristics are analysed, providing a solid theoretical foundation for the large-scale production and application of co-pyrolysis. Besides the potential problems related to plastic co-pyrolysis, the enhancement of carbon materials’ properties by plastic waste in co-pyrolysis is also explored, which is significant for the functionalization of carbon materials. The reaction mechanism, reaction process, reaction conditions, and products generated from the co-pyrolysis of biomass and plastic waste are discussed. In the co-pyrolysis of biomass (especially lignocellulosic biomass) and plastic waste, PET, PU, and PVC are more conducive to the production of carbon materials, while PP, PE, and PS are more favourable for the generation of bio-oils. The interaction between the hydroxyl radicals provided by biomass and the hydrogen radicals provided by plastic waste enhances the reaction. Slow co-pyrolysis at 500 °C, a feedstock ratio of 3 : 1 (biomass to plastic waste), and a suitable catalyst (such as zeolites) are more beneficial for carbon materials in terms of the yield, porosity, and production rate. Co-pyrolysis carbon materials possess superior hydrophobicity and adsorption properties compared to conventional carbon materials and can be enriched in elements often absent from the original carbon materials, such as nitrogen. These potential advantages of co-pyrolyzing plastics with biomass open new prospects beyond waste management, such as enhanced material development for a range of environmental and agricultural applications.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.