{"title":"热解生物油催化加氢脱氧生成喷气燃料:综述","authors":"Zhongyang Luo, Wanchen Zhu, Feiting Miao, Jinsong Zhou","doi":"10.1007/s11708-024-0943-7","DOIUrl":null,"url":null,"abstract":"<div><p>Bio-oil from biomass pyrolysis cannot directly substitute traditional fuel due to compositional deficiencies. Catalytic hydrodeoxygenation (HDO) is the critical and efficient step to upgrade crude bio-oil to high-quality bio-jet fuel by lowering the oxygen content and increasing the heating value. However, the hydrocracking reaction tends to reduce the liquid yield and increase the gas yield, causing carbon loss and producing hydrocarbons with a short carbon-chain. To obtain high-yield bio-jet fuel, the elucidation of the conversion process of biomass catalytic HDO is important in providing guidance for metal catalyst design and optimization of reaction conditions. Considering the complexity of crude bio-oil, this review aimed to investigate the catalytic HDO pathways with model compounds that present typical bio-oil components. First, it provided a comprehensive summary of the impact of physical and electronic structures of both noble and non-noble metals that include monometallic and bimetallic supported catalysts on regulating the conversion pathways and resulting product selectivity. The subsequent first principle calculations further corroborated reaction pathways of model compounds in atom-level on different catalyst surfaces with the experiments above and illustrated the favored C–O/C=O scission orders thermodynamically and kinetically. Then, it discussed hydrogenation effects of different H-donors (such as hydrogen and methane) and catalysts deactivation for economical and industrial consideration. Based on the descriptions above and recent researches, it also elaborated on catalytic HDO of biomass and bio-oil with multi-functional catalysts. Finally, it presented the challenges and future prospective of biomass catalytic HDO.</p></div>","PeriodicalId":570,"journal":{"name":"Frontiers in Energy","volume":"18 5","pages":"550 - 582"},"PeriodicalIF":3.1000,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Catalytic hydrodeoxygenation of pyrolysis bio-oil to jet fuel: A review\",\"authors\":\"Zhongyang Luo, Wanchen Zhu, Feiting Miao, Jinsong Zhou\",\"doi\":\"10.1007/s11708-024-0943-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Bio-oil from biomass pyrolysis cannot directly substitute traditional fuel due to compositional deficiencies. Catalytic hydrodeoxygenation (HDO) is the critical and efficient step to upgrade crude bio-oil to high-quality bio-jet fuel by lowering the oxygen content and increasing the heating value. However, the hydrocracking reaction tends to reduce the liquid yield and increase the gas yield, causing carbon loss and producing hydrocarbons with a short carbon-chain. To obtain high-yield bio-jet fuel, the elucidation of the conversion process of biomass catalytic HDO is important in providing guidance for metal catalyst design and optimization of reaction conditions. Considering the complexity of crude bio-oil, this review aimed to investigate the catalytic HDO pathways with model compounds that present typical bio-oil components. First, it provided a comprehensive summary of the impact of physical and electronic structures of both noble and non-noble metals that include monometallic and bimetallic supported catalysts on regulating the conversion pathways and resulting product selectivity. The subsequent first principle calculations further corroborated reaction pathways of model compounds in atom-level on different catalyst surfaces with the experiments above and illustrated the favored C–O/C=O scission orders thermodynamically and kinetically. Then, it discussed hydrogenation effects of different H-donors (such as hydrogen and methane) and catalysts deactivation for economical and industrial consideration. Based on the descriptions above and recent researches, it also elaborated on catalytic HDO of biomass and bio-oil with multi-functional catalysts. 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引用次数: 0
摘要
由于成分缺陷,生物质热解产生的生物油不能直接替代传统燃料。催化加氢脱氧(HDO)是将粗生物油升级为优质生物喷气燃料的关键和高效步骤,可降低氧含量并提高热值。然而,加氢裂化反应往往会降低液体产率,增加气体产率,造成碳损失并产生碳链较短的碳氢化合物。为了获得高产生物喷气燃料,阐明生物质催化加氢脱氧的转化过程对于指导金属催化剂的设计和反应条件的优化非常重要。考虑到粗生物油的复杂性,本综述旨在利用呈现典型生物油成分的模型化合物研究催化 HDO 途径。首先,它全面总结了贵金属和非贵金属(包括单金属和双金属支撑催化剂)的物理和电子结构对调节转化途径和由此产生的产品选择性的影响。随后进行的第一性原理计算进一步证实了模型化合物在不同催化剂表面的原子级反应路径与上述实验之间的联系,并从热力学和动力学角度说明了有利的 C-O/C=O 裂解顺序。然后,从经济和工业角度讨论了不同 H 供体(如氢气和甲烷)的加氢效应和催化剂失活问题。根据上述描述和近期研究,还阐述了使用多功能催化剂催化生物质和生物油的 HDO。最后,报告介绍了生物质催化脱氧的挑战和未来前景。
Catalytic hydrodeoxygenation of pyrolysis bio-oil to jet fuel: A review
Bio-oil from biomass pyrolysis cannot directly substitute traditional fuel due to compositional deficiencies. Catalytic hydrodeoxygenation (HDO) is the critical and efficient step to upgrade crude bio-oil to high-quality bio-jet fuel by lowering the oxygen content and increasing the heating value. However, the hydrocracking reaction tends to reduce the liquid yield and increase the gas yield, causing carbon loss and producing hydrocarbons with a short carbon-chain. To obtain high-yield bio-jet fuel, the elucidation of the conversion process of biomass catalytic HDO is important in providing guidance for metal catalyst design and optimization of reaction conditions. Considering the complexity of crude bio-oil, this review aimed to investigate the catalytic HDO pathways with model compounds that present typical bio-oil components. First, it provided a comprehensive summary of the impact of physical and electronic structures of both noble and non-noble metals that include monometallic and bimetallic supported catalysts on regulating the conversion pathways and resulting product selectivity. The subsequent first principle calculations further corroborated reaction pathways of model compounds in atom-level on different catalyst surfaces with the experiments above and illustrated the favored C–O/C=O scission orders thermodynamically and kinetically. Then, it discussed hydrogenation effects of different H-donors (such as hydrogen and methane) and catalysts deactivation for economical and industrial consideration. Based on the descriptions above and recent researches, it also elaborated on catalytic HDO of biomass and bio-oil with multi-functional catalysts. Finally, it presented the challenges and future prospective of biomass catalytic HDO.
期刊介绍:
Frontiers in Energy, an interdisciplinary and peer-reviewed international journal launched in January 2007, seeks to provide a rapid and unique platform for reporting the most advanced research on energy technology and strategic thinking in order to promote timely communication between researchers, scientists, engineers, and policy makers in the field of energy.
Frontiers in Energy aims to be a leading peer-reviewed platform and an authoritative source of information for analyses, reviews and evaluations in energy engineering and research, with a strong focus on energy analysis, energy modelling and prediction, integrated energy systems, energy conversion and conservation, energy planning and energy on economic and policy issues.
Frontiers in Energy publishes state-of-the-art review articles, original research papers and short communications by individual researchers or research groups. It is strictly peer-reviewed and accepts only original submissions in English. The scope of the journal is broad and covers all latest focus in current energy research.
High-quality papers are solicited in, but are not limited to the following areas:
-Fundamental energy science
-Energy technology, including energy generation, conversion, storage, renewables, transport, urban design and building efficiency
-Energy and the environment, including pollution control, energy efficiency and climate change
-Energy economics, strategy and policy
-Emerging energy issue