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Effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol

K(3)PO(4)/NaX catalysts were prepared by loading potassium phosphate on NaX zeolite, and the catalytic performance was studied for the side-chain alkylation of toluene with methanol to styrene and ethylbenzene. Combined with the characterization of XRD, TPD-NH(3), TPD-CO(2), and FTIR and the determi...

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Autores principales: Li, Huijun, Wang, Bin, Wen, Yueli, Hao, Chunyao, Liu, Yuhua, Huang, Wei
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/PMC8697353/
https://www.ncbi.nlm.nih.gov/pubmed/35423809
http://dx.doi.org/10.1039/d1ra00263e
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author Li, Huijun
Wang, Bin
Wen, Yueli
Hao, Chunyao
Liu, Yuhua
Huang, Wei
author_facet Li, Huijun
Wang, Bin
Wen, Yueli
Hao, Chunyao
Liu, Yuhua
Huang, Wei
author_sort Li, Huijun
collection PubMed
description K(3)PO(4)/NaX catalysts were prepared by loading potassium phosphate on NaX zeolite, and the catalytic performance was studied for the side-chain alkylation of toluene with methanol to styrene and ethylbenzene. Combined with the characterization of XRD, TPD-NH(3), TPD-CO(2), and FTIR and the determination of phosphorus content, it is revealed that firstly, the P element loaded on the catalyst surface can prominently promote the percentage of middle base sites, which will accordingly enhance the selectivity of the products (styrene and ethylbenzene) of side-chain alkylation of toluene; secondly, if there are enough middle base sites distributed on the catalysts, the higher percentage of strong base sites benefit the selectivity of styrene, which is confirmed by the performance of the two-stage catalysts.
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spelling pubmed-86973532022-04-13 Effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol Li, Huijun Wang, Bin Wen, Yueli Hao, Chunyao Liu, Yuhua Huang, Wei RSC Adv Chemistry K(3)PO(4)/NaX catalysts were prepared by loading potassium phosphate on NaX zeolite, and the catalytic performance was studied for the side-chain alkylation of toluene with methanol to styrene and ethylbenzene. Combined with the characterization of XRD, TPD-NH(3), TPD-CO(2), and FTIR and the determination of phosphorus content, it is revealed that firstly, the P element loaded on the catalyst surface can prominently promote the percentage of middle base sites, which will accordingly enhance the selectivity of the products (styrene and ethylbenzene) of side-chain alkylation of toluene; secondly, if there are enough middle base sites distributed on the catalysts, the higher percentage of strong base sites benefit the selectivity of styrene, which is confirmed by the performance of the two-stage catalysts. The Royal Society of Chemistry 2021-04-08 /pmc/articles/PMC8697353/ /pubmed/35423809 http://dx.doi.org/10.1039/d1ra00263e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Li, Huijun
Wang, Bin
Wen, Yueli
Hao, Chunyao
Liu, Yuhua
Huang, Wei
Effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol
title Effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol
title_full Effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol
title_fullStr Effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol
title_full_unstemmed Effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol
title_short Effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol
title_sort effect of relative percentage of acid and base sites on the side-chain alkylation of toluene with methanol
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697353/
https://www.ncbi.nlm.nih.gov/pubmed/35423809
http://dx.doi.org/10.1039/d1ra00263e
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