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Synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone

New solid acid catalysts were prepared by bisphenol A, paraformaldehyde and chlorosulfonic acid, and applied to hydroxylalkylation/alkylation (HAA) of 2-methylfuran (2-MF) and cyclohexanone. After optimizing the reaction conditions, the conversion of 2-MF reached 99% and the yield of 5,5′-(cyclohexa...

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Autores principales: Sun, Shaoying, Zhang, Xing, Li, Yanqing, Shao, Xianzhao, Ji, Jianwei, Liu, Junhai, Wang, Wei, Li, Zhizhou, Ji, Xiaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048630/
https://www.ncbi.nlm.nih.gov/pubmed/35496336
http://dx.doi.org/10.1039/d2ra01987f
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author Sun, Shaoying
Zhang, Xing
Li, Yanqing
Shao, Xianzhao
Ji, Jianwei
Liu, Junhai
Wang, Wei
Li, Zhizhou
Ji, Xiaohui
author_facet Sun, Shaoying
Zhang, Xing
Li, Yanqing
Shao, Xianzhao
Ji, Jianwei
Liu, Junhai
Wang, Wei
Li, Zhizhou
Ji, Xiaohui
author_sort Sun, Shaoying
collection PubMed
description New solid acid catalysts were prepared by bisphenol A, paraformaldehyde and chlorosulfonic acid, and applied to hydroxylalkylation/alkylation (HAA) of 2-methylfuran (2-MF) and cyclohexanone. After optimizing the reaction conditions, the conversion of 2-MF reached 99% and the yield of 5,5′-(cyclohexane-1,1-diyl)bis(2-methylfuran) acquired 98%. The activity and catalytic efficiency were higher than those of Amberlyst 15 and Amberlyst 36 resins, which could be rationalized by high acid strength. At the same time, the catalysts were characterized by acid–base titration and FTIR. Hydrodeoxygenation (HDO) of HAA products of 2-methylfuran and cyclopentanone were processed on the Ni/SiO(2) catalyst prepared by wet impregnation method to further convert into aviation kerosene, and the yield reached 93%.
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spelling pubmed-90486302022-04-28 Synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone Sun, Shaoying Zhang, Xing Li, Yanqing Shao, Xianzhao Ji, Jianwei Liu, Junhai Wang, Wei Li, Zhizhou Ji, Xiaohui RSC Adv Chemistry New solid acid catalysts were prepared by bisphenol A, paraformaldehyde and chlorosulfonic acid, and applied to hydroxylalkylation/alkylation (HAA) of 2-methylfuran (2-MF) and cyclohexanone. After optimizing the reaction conditions, the conversion of 2-MF reached 99% and the yield of 5,5′-(cyclohexane-1,1-diyl)bis(2-methylfuran) acquired 98%. The activity and catalytic efficiency were higher than those of Amberlyst 15 and Amberlyst 36 resins, which could be rationalized by high acid strength. At the same time, the catalysts were characterized by acid–base titration and FTIR. Hydrodeoxygenation (HDO) of HAA products of 2-methylfuran and cyclopentanone were processed on the Ni/SiO(2) catalyst prepared by wet impregnation method to further convert into aviation kerosene, and the yield reached 93%. The Royal Society of Chemistry 2022-04-28 /pmc/articles/PMC9048630/ /pubmed/35496336 http://dx.doi.org/10.1039/d2ra01987f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Sun, Shaoying
Zhang, Xing
Li, Yanqing
Shao, Xianzhao
Ji, Jianwei
Liu, Junhai
Wang, Wei
Li, Zhizhou
Ji, Xiaohui
Synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone
title Synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone
title_full Synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone
title_fullStr Synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone
title_full_unstemmed Synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone
title_short Synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone
title_sort synthesis of renewable diesel and jet fuel range alkanes using 2-methylfuran and cyclohexanone
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048630/
https://www.ncbi.nlm.nih.gov/pubmed/35496336
http://dx.doi.org/10.1039/d2ra01987f
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