Issue 4, 2023

Hydrophobically modified mesoporous silica supported Pt as a dual-function adsorbent buffer-catalyst for toluene removal under low-temperature

Abstract

A bifunctional adsorption-catalysis system for the abatement of trace amounts of toluene was developed and realized by loading different amounts of Pt on mesoporous silica synthesized with ionic liquid with hydrophobic modification. The textural properties were evaluated using BET, contact angle, XRD, IR, XPS, TEM, and H2-TPR techniques. The capability of the synthesized catalysts for room-temperature adsorption and low-temperature catalysis of toluene was appraised. The hydrophobic sample exhibited better toluene adsorption capacity of 53.1 mg g−1 than SiO2-350 and 3.0Pt/SiO2 samples with 28.3 mg g−1 and 18.9 mg g−1, respectively. Furthermore, the hydrophobic sample showed increased maximum desorption temperatures of 52 °C in comparison with those at 44 °C and 37 °C, which acted as a good adsorption buffering system. 3.0Pt/SiO2-H showed the best toluene conversion capacity at T90 = 129 °C, together with superior water vapor resistance and sequential capture-destruction performances. The increased bifunctional adsorption-catalysis performance with hydrophobic modification may be ascribed to the change in surface functional groups. The prepared system could be a valuable candidate material for adsorption-catalysis integration and assistance for VOCs elimination technology in barren waste gases.

Graphical abstract: Hydrophobically modified mesoporous silica supported Pt as a dual-function adsorbent buffer-catalyst for toluene removal under low-temperature

Supplementary files

Article information

Article type
Paper
Submitted
27 Sep 2022
Accepted
30 Nov 2022
First published
22 Dec 2022

New J. Chem., 2023,47, 1767-1776

Hydrophobically modified mesoporous silica supported Pt as a dual-function adsorbent buffer-catalyst for toluene removal under low-temperature

M. Zhou, S. Li, S. Chai, T. Wang, L. Nie and Y. Chen, New J. Chem., 2023, 47, 1767 DOI: 10.1039/D2NJ04768C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements