Cargando…

Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach

Sulfided nickel, an established hydrocracking and hydrotreating catalyst for hydrocarbon refining, was synthesized on porous aluminosilicate supports for the hydrocracking of mixed polyolefin waste. Zeolite beta, zeolite 13X, MCM41 and an amorphous silica-alumina catalyst support were impregnated wi...

Descripción completa

Detalles Bibliográficos
Autores principales: Tedstone, Aleksander A., Bin Jumah, Abdulrahman, Asuquo, Edidiong, Garforth, Arthur A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924768/
https://www.ncbi.nlm.nih.gov/pubmed/35308628
http://dx.doi.org/10.1098/rsos.211353
_version_ 1784669930058153984
author Tedstone, Aleksander A.
Bin Jumah, Abdulrahman
Asuquo, Edidiong
Garforth, Arthur A.
author_facet Tedstone, Aleksander A.
Bin Jumah, Abdulrahman
Asuquo, Edidiong
Garforth, Arthur A.
author_sort Tedstone, Aleksander A.
collection PubMed
description Sulfided nickel, an established hydrocracking and hydrotreating catalyst for hydrocarbon refining, was synthesized on porous aluminosilicate supports for the hydrocracking of mixed polyolefin waste. Zeolite beta, zeolite 13X, MCM41 and an amorphous silica-alumina catalyst support were impregnated with the single-source precursor (SSP) nickel (II) ethylxanthate for catalyst support screening. Application of this synthesis method to beta-supported nickel (Ni@Beta), as an alternative to wet impregnation using aqueous nickel (II) nitrate, provided catalytic materials with higher conversion to fluid products at the same mild batch reaction conditions of 330°C with appropriate agitation and 20 bar H(2) pressure. Mass balance quantification demonstrated that SSP-derived 5wt%Ni@Beta yielded a greater than 95 wt% conversion of a mixed polyolefin feed to fluid products, compared with 39.8 wt% conversion in the case of 5wt%Ni@Beta prepared by wet impregnation. Liquid and gas products were quantitatively analysed by gas chromatography–flame ionization detection (GC-FID) and gas chromatography–mass spectrometry (GC-MS), revealing a strong selectivity to saturated C(4) (37.3 wt%), C(5) (21.6 wt%) and C(6) (12.8 wt%) hydrocarbons in the case of the SSP-derived catalyst.
format Online
Article
Text
id pubmed-8924768
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-89247682022-03-17 Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach Tedstone, Aleksander A. Bin Jumah, Abdulrahman Asuquo, Edidiong Garforth, Arthur A. R Soc Open Sci Chemistry Sulfided nickel, an established hydrocracking and hydrotreating catalyst for hydrocarbon refining, was synthesized on porous aluminosilicate supports for the hydrocracking of mixed polyolefin waste. Zeolite beta, zeolite 13X, MCM41 and an amorphous silica-alumina catalyst support were impregnated with the single-source precursor (SSP) nickel (II) ethylxanthate for catalyst support screening. Application of this synthesis method to beta-supported nickel (Ni@Beta), as an alternative to wet impregnation using aqueous nickel (II) nitrate, provided catalytic materials with higher conversion to fluid products at the same mild batch reaction conditions of 330°C with appropriate agitation and 20 bar H(2) pressure. Mass balance quantification demonstrated that SSP-derived 5wt%Ni@Beta yielded a greater than 95 wt% conversion of a mixed polyolefin feed to fluid products, compared with 39.8 wt% conversion in the case of 5wt%Ni@Beta prepared by wet impregnation. Liquid and gas products were quantitatively analysed by gas chromatography–flame ionization detection (GC-FID) and gas chromatography–mass spectrometry (GC-MS), revealing a strong selectivity to saturated C(4) (37.3 wt%), C(5) (21.6 wt%) and C(6) (12.8 wt%) hydrocarbons in the case of the SSP-derived catalyst. The Royal Society 2022-03-16 /pmc/articles/PMC8924768/ /pubmed/35308628 http://dx.doi.org/10.1098/rsos.211353 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Chemistry
Tedstone, Aleksander A.
Bin Jumah, Abdulrahman
Asuquo, Edidiong
Garforth, Arthur A.
Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach
title Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach
title_full Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach
title_fullStr Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach
title_full_unstemmed Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach
title_short Transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach
title_sort transition metal chalcogenide bifunctional catalysts for chemical recycling by plastic hydrocracking: a single-source precursor approach
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924768/
https://www.ncbi.nlm.nih.gov/pubmed/35308628
http://dx.doi.org/10.1098/rsos.211353
work_keys_str_mv AT tedstonealeksandera transitionmetalchalcogenidebifunctionalcatalystsforchemicalrecyclingbyplastichydrocrackingasinglesourceprecursorapproach
AT binjumahabdulrahman transitionmetalchalcogenidebifunctionalcatalystsforchemicalrecyclingbyplastichydrocrackingasinglesourceprecursorapproach
AT asuquoedidiong transitionmetalchalcogenidebifunctionalcatalystsforchemicalrecyclingbyplastichydrocrackingasinglesourceprecursorapproach
AT garfortharthura transitionmetalchalcogenidebifunctionalcatalystsforchemicalrecyclingbyplastichydrocrackingasinglesourceprecursorapproach