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Enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride

Hydrogen-type mordenite (HMOR) modified with pyrazole hydrochloride (Pya·HCl) was prepared by the ion exchange method. The results showed that Pya·HCl introduction significantly improved the activity and stability of HMOR in the carbonylation reaction of dimethyl ether (DME) to methyl acetate (MA)....

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Detalles Bibliográficos
Autores principales: Liu, Yiyin, Shen, Yiyang, Geng, Jianming, Dong, Xinfa
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/PMC8978611/
https://www.ncbi.nlm.nih.gov/pubmed/35424504
http://dx.doi.org/10.1039/d1ra08235c
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author Liu, Yiyin
Shen, Yiyang
Geng, Jianming
Dong, Xinfa
author_facet Liu, Yiyin
Shen, Yiyang
Geng, Jianming
Dong, Xinfa
author_sort Liu, Yiyin
collection PubMed
description Hydrogen-type mordenite (HMOR) modified with pyrazole hydrochloride (Pya·HCl) was prepared by the ion exchange method. The results showed that Pya·HCl introduction significantly improved the activity and stability of HMOR in the carbonylation reaction of dimethyl ether (DME) to methyl acetate (MA). Small pyrazole ions (HPya(+)) entered into the twelve-membered ring (12-MR) pores of HMOR and selectively replaced part of the Brønsted acid (BAS), thus suppressing the formation of carbon deposits. The modified HMOR presented a larger specific surface area and pore volume, which provided larger channels for molecular diffusion. Additionally, non-framework aluminum was removed by the acidic Pya·HCl solution, resulting in the formation of mesopores, which facilitated the migration of carbon-deposited species from the inside of the zeolite to the outside.
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spelling pubmed-89786112022-04-13 Enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride Liu, Yiyin Shen, Yiyang Geng, Jianming Dong, Xinfa RSC Adv Chemistry Hydrogen-type mordenite (HMOR) modified with pyrazole hydrochloride (Pya·HCl) was prepared by the ion exchange method. The results showed that Pya·HCl introduction significantly improved the activity and stability of HMOR in the carbonylation reaction of dimethyl ether (DME) to methyl acetate (MA). Small pyrazole ions (HPya(+)) entered into the twelve-membered ring (12-MR) pores of HMOR and selectively replaced part of the Brønsted acid (BAS), thus suppressing the formation of carbon deposits. The modified HMOR presented a larger specific surface area and pore volume, which provided larger channels for molecular diffusion. Additionally, non-framework aluminum was removed by the acidic Pya·HCl solution, resulting in the formation of mesopores, which facilitated the migration of carbon-deposited species from the inside of the zeolite to the outside. The Royal Society of Chemistry 2021-12-21 /pmc/articles/PMC8978611/ /pubmed/35424504 http://dx.doi.org/10.1039/d1ra08235c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Liu, Yiyin
Shen, Yiyang
Geng, Jianming
Dong, Xinfa
Enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride
title Enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride
title_full Enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride
title_fullStr Enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride
title_full_unstemmed Enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride
title_short Enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride
title_sort enhancing the dimethyl ether carbonylation performance over hydrogen-type mordenites modified by pyrazole hydrochloride
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8978611/
https://www.ncbi.nlm.nih.gov/pubmed/35424504
http://dx.doi.org/10.1039/d1ra08235c
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