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Sn(II)/PN@AC catalysts: synthesis, physical-chemical characterization, and applications
In this study, the novel tin-based catalysts (Sn(II)/PN@AC) were prepared using the phosphorus and nitrogen dual-modified activated carbon as support and SnCl(2) as active compounds, as well as then evaluated in acetylene hydrochlorination. Under the reaction temperature of 180 °C and an acetylene g...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Scientific and Technological Research Council of Turkey
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596525/ https://www.ncbi.nlm.nih.gov/pubmed/34849061 http://dx.doi.org/10.3906/kim-2103-9 |
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author | WU, Yibo LI, Fuxiang LI, Qinbin HAN, Yongjun WANG, Li MA, Wei XV, Fu |
author_facet | WU, Yibo LI, Fuxiang LI, Qinbin HAN, Yongjun WANG, Li MA, Wei XV, Fu |
author_sort | WU, Yibo |
collection | PubMed |
description | In this study, the novel tin-based catalysts (Sn(II)/PN@AC) were prepared using the phosphorus and nitrogen dual-modified activated carbon as support and SnCl(2) as active compounds, as well as then evaluated in acetylene hydrochlorination. Under the reaction temperature of 180 °C and an acetylene gas hourly space velocity (GHSV-C(2)H(2)) of 30 h(–1), the 15%Sn(II)/PN@AC-550 showed the initial acetylene conversion of 100% and vinyl chloride selectivity over 98.5%. Additionally, the deactivation rate of 15%Sn(II)/PN@AC-550 reached 0.47% h(–1), which was lower than that of 15%Sn(II)/AC-550 (1.02% h(–1)), suggesting that PN@AC-550 as novel support can retarded the deactivation of Sn(II)/AC-550 catalysts during acetylene hydrochlorination. Based on the catalytic tests and characterization results (XRD, Raman, BET surface area, TEM, C(2)H(2)-TPD, H(2)-TPR, XPS, FT-IR, TGA, and ICP), it demonstrated that PN@AC-550 as support could effectively improve the dispersion of tin species, retard the formation of coke deposition, lessen the oxidation of SnCl(2) during the preparation process, as well as relatively inhibit the leach of tin species during the reaction. By combing the FTIR results and Rideal–Eley mechanism, we proposed that that HSnCl(3) was transition state of SnCl(2) in catalysis acetylene hydrochlorination and then adsorbed the acetylene to produce the vinyl chloride. |
format | Online Article Text |
id | pubmed-8596525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Scientific and Technological Research Council of Turkey |
record_format | MEDLINE/PubMed |
spelling | pubmed-85965252021-11-29 Sn(II)/PN@AC catalysts: synthesis, physical-chemical characterization, and applications WU, Yibo LI, Fuxiang LI, Qinbin HAN, Yongjun WANG, Li MA, Wei XV, Fu Turk J Chem Article In this study, the novel tin-based catalysts (Sn(II)/PN@AC) were prepared using the phosphorus and nitrogen dual-modified activated carbon as support and SnCl(2) as active compounds, as well as then evaluated in acetylene hydrochlorination. Under the reaction temperature of 180 °C and an acetylene gas hourly space velocity (GHSV-C(2)H(2)) of 30 h(–1), the 15%Sn(II)/PN@AC-550 showed the initial acetylene conversion of 100% and vinyl chloride selectivity over 98.5%. Additionally, the deactivation rate of 15%Sn(II)/PN@AC-550 reached 0.47% h(–1), which was lower than that of 15%Sn(II)/AC-550 (1.02% h(–1)), suggesting that PN@AC-550 as novel support can retarded the deactivation of Sn(II)/AC-550 catalysts during acetylene hydrochlorination. Based on the catalytic tests and characterization results (XRD, Raman, BET surface area, TEM, C(2)H(2)-TPD, H(2)-TPR, XPS, FT-IR, TGA, and ICP), it demonstrated that PN@AC-550 as support could effectively improve the dispersion of tin species, retard the formation of coke deposition, lessen the oxidation of SnCl(2) during the preparation process, as well as relatively inhibit the leach of tin species during the reaction. By combing the FTIR results and Rideal–Eley mechanism, we proposed that that HSnCl(3) was transition state of SnCl(2) in catalysis acetylene hydrochlorination and then adsorbed the acetylene to produce the vinyl chloride. The Scientific and Technological Research Council of Turkey 2021-10-19 /pmc/articles/PMC8596525/ /pubmed/34849061 http://dx.doi.org/10.3906/kim-2103-9 Text en Copyright © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This article is distributed 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 and redistribution provided that the original author and source are credited. |
spellingShingle | Article WU, Yibo LI, Fuxiang LI, Qinbin HAN, Yongjun WANG, Li MA, Wei XV, Fu Sn(II)/PN@AC catalysts: synthesis, physical-chemical characterization, and applications |
title | Sn(II)/PN@AC catalysts: synthesis, physical-chemical characterization, and applications |
title_full | Sn(II)/PN@AC catalysts: synthesis, physical-chemical characterization, and applications |
title_fullStr | Sn(II)/PN@AC catalysts: synthesis, physical-chemical characterization, and applications |
title_full_unstemmed | Sn(II)/PN@AC catalysts: synthesis, physical-chemical characterization, and applications |
title_short | Sn(II)/PN@AC catalysts: synthesis, physical-chemical characterization, and applications |
title_sort | sn(ii)/pn@ac catalysts: synthesis, physical-chemical characterization, and applications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596525/ https://www.ncbi.nlm.nih.gov/pubmed/34849061 http://dx.doi.org/10.3906/kim-2103-9 |
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