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Modifying Y zeolite with chloropropyl for improving Cu load on Y zeolite as a super Cu/Y catalyst for toluene oxidation
Developing an efficient catalyst is desirable when for example moving from a noble metal-based catalyst to a transition metal-based one for VOC removal. In this work, the chloropropyl-modified NaY zeolite (NaY-CPT) was first synthesized in an extremely dense system through introducing 3-chloropropyl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043743/ https://www.ncbi.nlm.nih.gov/pubmed/35496414 http://dx.doi.org/10.1039/d1ra06469j |
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author | Meng, Xiaoling Meng, Lingke Gong, Yanjun Li, Zhihong Mo, Guang Zhang, Jing |
author_facet | Meng, Xiaoling Meng, Lingke Gong, Yanjun Li, Zhihong Mo, Guang Zhang, Jing |
author_sort | Meng, Xiaoling |
collection | PubMed |
description | Developing an efficient catalyst is desirable when for example moving from a noble metal-based catalyst to a transition metal-based one for VOC removal. In this work, the chloropropyl-modified NaY zeolite (NaY-CPT) was first synthesized in an extremely dense system through introducing 3-chloropropyl-trimethoxysilane (CPT) in the aluminosilicate sol. Then the Cu/Y-CPT catalyst was fabricated by impregnating Cu species on the NaY-CPT zeolite and the highly effective Cu/Y based catalyst has been achieved for catalytic toluene oxidation. The structure evolution of CPT modified sol and its effect on texture properties of NaY-CPT and thereby reduction ability of Cu/Y catalyst were systematically investigated by synchrotron radiation small angle X-ray scattering (SR-SAXS), EXAFS and other characterization. The CPT modified sol can promote the formation of more active aluminosilicate species, greatly accelerating crystal growth and improving framework Si/Al ratio of NaY zeolite. Due to the presence of the CPT group, the Cu/Y-CPT catalyst enhanced the interaction between Cu species and the zeolite matrix, resulting in small sized CuO nanoparticles (2.0–4.0 nm) anchoring to NaY-CPT. The Cu/Y-CPT catalyst renders more isolated Cu(2+) species and adsorbed oxygen species, which are reactive in the oxidation reaction due to their high reducibility and mobility. Finally, the Cu/Y-CPT catalyst exhibits 90% toluene conversion at 296 °C (T(90)), lower than the value of 375 °C on the conventional Cu/Y-con catalyst. Meanwhile, the optimal Cu/Y-CPT catalyst also gives higher toluene conversion and stability in moisture conditions. |
format | Online Article Text |
id | pubmed-9043743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90437432022-04-28 Modifying Y zeolite with chloropropyl for improving Cu load on Y zeolite as a super Cu/Y catalyst for toluene oxidation Meng, Xiaoling Meng, Lingke Gong, Yanjun Li, Zhihong Mo, Guang Zhang, Jing RSC Adv Chemistry Developing an efficient catalyst is desirable when for example moving from a noble metal-based catalyst to a transition metal-based one for VOC removal. In this work, the chloropropyl-modified NaY zeolite (NaY-CPT) was first synthesized in an extremely dense system through introducing 3-chloropropyl-trimethoxysilane (CPT) in the aluminosilicate sol. Then the Cu/Y-CPT catalyst was fabricated by impregnating Cu species on the NaY-CPT zeolite and the highly effective Cu/Y based catalyst has been achieved for catalytic toluene oxidation. The structure evolution of CPT modified sol and its effect on texture properties of NaY-CPT and thereby reduction ability of Cu/Y catalyst were systematically investigated by synchrotron radiation small angle X-ray scattering (SR-SAXS), EXAFS and other characterization. The CPT modified sol can promote the formation of more active aluminosilicate species, greatly accelerating crystal growth and improving framework Si/Al ratio of NaY zeolite. Due to the presence of the CPT group, the Cu/Y-CPT catalyst enhanced the interaction between Cu species and the zeolite matrix, resulting in small sized CuO nanoparticles (2.0–4.0 nm) anchoring to NaY-CPT. The Cu/Y-CPT catalyst renders more isolated Cu(2+) species and adsorbed oxygen species, which are reactive in the oxidation reaction due to their high reducibility and mobility. Finally, the Cu/Y-CPT catalyst exhibits 90% toluene conversion at 296 °C (T(90)), lower than the value of 375 °C on the conventional Cu/Y-con catalyst. Meanwhile, the optimal Cu/Y-CPT catalyst also gives higher toluene conversion and stability in moisture conditions. The Royal Society of Chemistry 2021-11-22 /pmc/articles/PMC9043743/ /pubmed/35496414 http://dx.doi.org/10.1039/d1ra06469j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Meng, Xiaoling Meng, Lingke Gong, Yanjun Li, Zhihong Mo, Guang Zhang, Jing Modifying Y zeolite with chloropropyl for improving Cu load on Y zeolite as a super Cu/Y catalyst for toluene oxidation |
title | Modifying Y zeolite with chloropropyl for improving Cu load on Y zeolite as a super Cu/Y catalyst for toluene oxidation |
title_full | Modifying Y zeolite with chloropropyl for improving Cu load on Y zeolite as a super Cu/Y catalyst for toluene oxidation |
title_fullStr | Modifying Y zeolite with chloropropyl for improving Cu load on Y zeolite as a super Cu/Y catalyst for toluene oxidation |
title_full_unstemmed | Modifying Y zeolite with chloropropyl for improving Cu load on Y zeolite as a super Cu/Y catalyst for toluene oxidation |
title_short | Modifying Y zeolite with chloropropyl for improving Cu load on Y zeolite as a super Cu/Y catalyst for toluene oxidation |
title_sort | modifying y zeolite with chloropropyl for improving cu load on y zeolite as a super cu/y catalyst for toluene oxidation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9043743/ https://www.ncbi.nlm.nih.gov/pubmed/35496414 http://dx.doi.org/10.1039/d1ra06469j |
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