Shan Jiang , Riyang Shu , Anqi Wang , Zhuoli Deng , Yuhong Xiao , Jiajin Li , Qingwei Meng , Qian Zhang
{"title":"Efficient hydrodeoxygenation of lignin-derived phenolic compounds under acid-free conditions over carbon-supported NiMo catalysts†","authors":"Shan Jiang , Riyang Shu , Anqi Wang , Zhuoli Deng , Yuhong Xiao , Jiajin Li , Qingwei Meng , Qian Zhang","doi":"10.1039/d4gc02298j","DOIUrl":null,"url":null,"abstract":"<div><p>High-quality liquid biofuels can be produced from renewable lignin-derived phenolic compounds through an efficient hydrodeoxygenation (HDO) process in which the traditional catalysts usually include metal sites and acid sites that catalyze the hydrogenation and deoxygenation procedures respectively. This work presents a novel acid-free Ni<sub>x</sub>Mo<sub>y</sub>N/C catalyst from the perspective of green chemistry providing a new pathway for HDO of lignin-derived phenolic compounds that involves hydrogenation deoxygenation and hydrogenolysis at the same time. A series of Ni<sub>x</sub>Mo<sub>y</sub>N/C catalysts were prepared by varying the Ni : Mo molar ratio among which the Ni<sub>1</sub>Mo<sub>3</sub>N/C catalyst showed the best HDO performance. Guaiacol could be completely converted at 260 °C after 4 h with 95.8% cyclohexane selectivity. In addition a small amount of benzene could be obtained as a valuable fuel additive by-product by altering the conventional HDO reaction path. By shortening the reaction time benzene could be obtained as an intermediate product with a relative high selectivity. Based on the characterizations using XRD BET SEM TEM XPS H<sub>2</sub>-TPD and EPR, the results demonstrate that the multiple active components of the Ni<sub>1</sub>Mo<sub>3</sub>N/C catalyst allow it to efficiently catalyze the hydrogen activation and C–O bond cleavage even under acid-free conditions. The existence of the active phases of Ni Ni<sub>2</sub>Mo<sub>3</sub>N and β-Mo<sub>2</sub>C as well as the interaction between Ni and Mo metals together contributed toward efficient HDO performance. Not only for the various phenolic model compounds the feasibility of Ni<sub>1</sub>Mo<sub>3</sub>N/C catalysts for upgrading raw lignin oil was also demonstrated with the hydrocarbon content increasing from 5.7% to 88.4%. Notably arenes accounted for 18.2% of the hydrocarbon products which confirmed the occurrence of hydrogenolysis in the catalytic process. This work provides a novel route for the conversion of lignin-derived phenolic compounds to produce high-quality hydrocarbon liquid biofuels especially the direct production of arene components.</p></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"26 17","pages":"Pages 9330-9345"},"PeriodicalIF":9.2000,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926224007118","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
High-quality liquid biofuels can be produced from renewable lignin-derived phenolic compounds through an efficient hydrodeoxygenation (HDO) process in which the traditional catalysts usually include metal sites and acid sites that catalyze the hydrogenation and deoxygenation procedures respectively. This work presents a novel acid-free NixMoyN/C catalyst from the perspective of green chemistry providing a new pathway for HDO of lignin-derived phenolic compounds that involves hydrogenation deoxygenation and hydrogenolysis at the same time. A series of NixMoyN/C catalysts were prepared by varying the Ni : Mo molar ratio among which the Ni1Mo3N/C catalyst showed the best HDO performance. Guaiacol could be completely converted at 260 °C after 4 h with 95.8% cyclohexane selectivity. In addition a small amount of benzene could be obtained as a valuable fuel additive by-product by altering the conventional HDO reaction path. By shortening the reaction time benzene could be obtained as an intermediate product with a relative high selectivity. Based on the characterizations using XRD BET SEM TEM XPS H2-TPD and EPR, the results demonstrate that the multiple active components of the Ni1Mo3N/C catalyst allow it to efficiently catalyze the hydrogen activation and C–O bond cleavage even under acid-free conditions. The existence of the active phases of Ni Ni2Mo3N and β-Mo2C as well as the interaction between Ni and Mo metals together contributed toward efficient HDO performance. Not only for the various phenolic model compounds the feasibility of Ni1Mo3N/C catalysts for upgrading raw lignin oil was also demonstrated with the hydrocarbon content increasing from 5.7% to 88.4%. Notably arenes accounted for 18.2% of the hydrocarbon products which confirmed the occurrence of hydrogenolysis in the catalytic process. This work provides a novel route for the conversion of lignin-derived phenolic compounds to produce high-quality hydrocarbon liquid biofuels especially the direct production of arene components.
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.