Cargando…

Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water

The hydrogenation of furan ring in the biomass-derived furans is of great importance for the conversion of biomass to valuable chemicals. Fabrication of high activity and selectivity catalyst for this hydrogenation under mild conditions was one of the focuses of this research. In this manuscript, Ui...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Yanliang, Deng, Dongsheng, Sui, Dong, Xie, Yanfu, Li, Dongmi, Duan, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956234/
https://www.ncbi.nlm.nih.gov/pubmed/31795102
http://dx.doi.org/10.3390/nano9121698
_version_ 1783487113756409856
author Yang, Yanliang
Deng, Dongsheng
Sui, Dong
Xie, Yanfu
Li, Dongmi
Duan, Ying
author_facet Yang, Yanliang
Deng, Dongsheng
Sui, Dong
Xie, Yanfu
Li, Dongmi
Duan, Ying
author_sort Yang, Yanliang
collection PubMed
description The hydrogenation of furan ring in the biomass-derived furans is of great importance for the conversion of biomass to valuable chemicals. Fabrication of high activity and selectivity catalyst for this hydrogenation under mild conditions was one of the focuses of this research. In this manuscript, UiO-66-v, in which vinyl bonded to the benzene ring, was first prepared. Then, the uniformly distributed vinyl was used as the reductant for the preparation of Pd/UiO-66-v. The catalyst was characterized by X-ray diffraction, thermogravimetric, N(2) physical adsorption/desorption, X-ray photoelectron spectroscopy, scanning electron microscope, transmission electron microscopy, energy dispersive spectrometer elemental mappings, and inductively coupled plasma atomic emission spectroscopy to find the Pd/UiO-66-v had a narrow palladium nanoparticles size of 3–5 nm and maintained the structure and thermal stability of UiO-66-v. The Pd/UiO-66-v was used for the hydrogenation of furfuryl alcohol to tetrahydrofurfuryl alcohol in water. 99% conversion of furfuryl alcohol was obtained with 90% selectivity to tetrahydrofurfuryl alcohol after reacted at 0.5 MPa H(2), 303 K for 12 h. The Pd/UiO-66-v was proved to be effective for the hydrogenation of furan ring in furans and could be used for at least five times.
format Online
Article
Text
id pubmed-6956234
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-69562342020-01-23 Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water Yang, Yanliang Deng, Dongsheng Sui, Dong Xie, Yanfu Li, Dongmi Duan, Ying Nanomaterials (Basel) Article The hydrogenation of furan ring in the biomass-derived furans is of great importance for the conversion of biomass to valuable chemicals. Fabrication of high activity and selectivity catalyst for this hydrogenation under mild conditions was one of the focuses of this research. In this manuscript, UiO-66-v, in which vinyl bonded to the benzene ring, was first prepared. Then, the uniformly distributed vinyl was used as the reductant for the preparation of Pd/UiO-66-v. The catalyst was characterized by X-ray diffraction, thermogravimetric, N(2) physical adsorption/desorption, X-ray photoelectron spectroscopy, scanning electron microscope, transmission electron microscopy, energy dispersive spectrometer elemental mappings, and inductively coupled plasma atomic emission spectroscopy to find the Pd/UiO-66-v had a narrow palladium nanoparticles size of 3–5 nm and maintained the structure and thermal stability of UiO-66-v. The Pd/UiO-66-v was used for the hydrogenation of furfuryl alcohol to tetrahydrofurfuryl alcohol in water. 99% conversion of furfuryl alcohol was obtained with 90% selectivity to tetrahydrofurfuryl alcohol after reacted at 0.5 MPa H(2), 303 K for 12 h. The Pd/UiO-66-v was proved to be effective for the hydrogenation of furan ring in furans and could be used for at least five times. MDPI 2019-11-28 /pmc/articles/PMC6956234/ /pubmed/31795102 http://dx.doi.org/10.3390/nano9121698 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yang, Yanliang
Deng, Dongsheng
Sui, Dong
Xie, Yanfu
Li, Dongmi
Duan, Ying
Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water
title Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water
title_full Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water
title_fullStr Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water
title_full_unstemmed Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water
title_short Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water
title_sort facile preparation of pd/uio-66-v for the conversion of furfuryl alcohol to tetrahydrofurfuryl alcohol under mild conditions in water
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956234/
https://www.ncbi.nlm.nih.gov/pubmed/31795102
http://dx.doi.org/10.3390/nano9121698
work_keys_str_mv AT yangyanliang facilepreparationofpduio66vfortheconversionoffurfurylalcoholtotetrahydrofurfurylalcoholundermildconditionsinwater
AT dengdongsheng facilepreparationofpduio66vfortheconversionoffurfurylalcoholtotetrahydrofurfurylalcoholundermildconditionsinwater
AT suidong facilepreparationofpduio66vfortheconversionoffurfurylalcoholtotetrahydrofurfurylalcoholundermildconditionsinwater
AT xieyanfu facilepreparationofpduio66vfortheconversionoffurfurylalcoholtotetrahydrofurfurylalcoholundermildconditionsinwater
AT lidongmi facilepreparationofpduio66vfortheconversionoffurfurylalcoholtotetrahydrofurfurylalcoholundermildconditionsinwater
AT duanying facilepreparationofpduio66vfortheconversionoffurfurylalcoholtotetrahydrofurfurylalcoholundermildconditionsinwater