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In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source

A new noble metal-free Ni–Co–P/HAP (hydroxyapatite) amorphous alloy catalyst was synthesized by an impregnation-chemical reduction method; the structure and properties of the catalysts were characterized by XRD, SEM, BET, XPS and DSC. Based on the model of the hydrodeoxygenation (HDO) of vanillin to...

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Autores principales: Duan, Mingxing, Cheng, Qingyan, Wang, Mingming, Wang, Yanji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695862/
https://www.ncbi.nlm.nih.gov/pubmed/35423576
http://dx.doi.org/10.1039/d1ra00979f
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author Duan, Mingxing
Cheng, Qingyan
Wang, Mingming
Wang, Yanji
author_facet Duan, Mingxing
Cheng, Qingyan
Wang, Mingming
Wang, Yanji
author_sort Duan, Mingxing
collection PubMed
description A new noble metal-free Ni–Co–P/HAP (hydroxyapatite) amorphous alloy catalyst was synthesized by an impregnation-chemical reduction method; the structure and properties of the catalysts were characterized by XRD, SEM, BET, XPS and DSC. Based on the model of the hydrodeoxygenation (HDO) of vanillin to 2-methoxy-4-methylphenol (MMP) with formic acid as a hydrogen source, the catalytic performance of the catalyst was studied. The results found that the Ni–Co–P/HAP catalyst exhibited excellent catalytic activity for the in situ HDO reaction of vanillin compared with Ni–P and Ni–Co–P. The conversion of vanillin could be high to 97.86% with MMP selectivity of 93.97% under optimized reaction conditions. In addition, mechanism studies have shown that the side reaction of carbocation and vanillyl alcohol (HMP) condensation can be effectively reduced with increasing the hydrogenation rate, thereby the selectivity of MMP was effectively increased.
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spelling pubmed-86958622022-04-13 In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source Duan, Mingxing Cheng, Qingyan Wang, Mingming Wang, Yanji RSC Adv Chemistry A new noble metal-free Ni–Co–P/HAP (hydroxyapatite) amorphous alloy catalyst was synthesized by an impregnation-chemical reduction method; the structure and properties of the catalysts were characterized by XRD, SEM, BET, XPS and DSC. Based on the model of the hydrodeoxygenation (HDO) of vanillin to 2-methoxy-4-methylphenol (MMP) with formic acid as a hydrogen source, the catalytic performance of the catalyst was studied. The results found that the Ni–Co–P/HAP catalyst exhibited excellent catalytic activity for the in situ HDO reaction of vanillin compared with Ni–P and Ni–Co–P. The conversion of vanillin could be high to 97.86% with MMP selectivity of 93.97% under optimized reaction conditions. In addition, mechanism studies have shown that the side reaction of carbocation and vanillyl alcohol (HMP) condensation can be effectively reduced with increasing the hydrogenation rate, thereby the selectivity of MMP was effectively increased. The Royal Society of Chemistry 2021-03-16 /pmc/articles/PMC8695862/ /pubmed/35423576 http://dx.doi.org/10.1039/d1ra00979f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Duan, Mingxing
Cheng, Qingyan
Wang, Mingming
Wang, Yanji
In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source
title In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source
title_full In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source
title_fullStr In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source
title_full_unstemmed In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source
title_short In situ hydrodeoxygenation of vanillin over Ni–Co–P/HAP with formic acid as a hydrogen source
title_sort in situ hydrodeoxygenation of vanillin over ni–co–p/hap with formic acid as a hydrogen source
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695862/
https://www.ncbi.nlm.nih.gov/pubmed/35423576
http://dx.doi.org/10.1039/d1ra00979f
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