Excellent Low-Temperature Formaldehyde Decomposition Performance over Pt Nanoparticles Directly Loaded on Cellulose Triacetate
Cellulose triacetate (CTA) was first applied as the catalytic support to load Pt nanoparticles for low-temperature formaldehyde (HCHO) decomposition. The room-temperature HCHO decomposition rate of the obtained catalyst (Pt/CTA) is 13.4 times and 4.3 times as high as that of the microcrystalline cel...
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Published in: | Industrial & engineering chemistry research Vol. 59; no. 50; pp. 21720 - 21728 |
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Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
American Chemical Society
16-12-2020
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Subjects: | |
Online Access: | Get full text |
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Summary: | Cellulose triacetate (CTA) was first applied as the catalytic support to load Pt nanoparticles for low-temperature formaldehyde (HCHO) decomposition. The room-temperature HCHO decomposition rate of the obtained catalyst (Pt/CTA) is 13.4 times and 4.3 times as high as that of the microcrystalline cellulose-supported Pt catalyst and Pt/TiO2 under the parallel preparation condition, respectively. With facile shaping, the CTA microsphere-supported Pt catalyst and the CTA film-supported Pt catalyst could also exhibit similar HCHO decomposition performance to that of the powdery one. Structural analyses showed that Pt nanoparticles (∼2.3 nm) could densely disperse on the small-area surface of Pt/CTA and provide abundant active sites. Moreover, only the HCHO molecules could slightly adsorb onto CTA, while other HCHO decomposition-related species absolutely could not. This is beneficial to the coordination of various steps of HCHO decomposition and the transfer of reaction species to vicinal active sites of Pt/CTA. HCHO-diffuse reflectance infrared Fourier transformed spectroscopy studies demonstrated that no species were accumulated on the Pt/CTA catalyst. Both the good Pt dispersion and unique adsorption properties of CTA were responsible for the excellent low-temperature HCHO decomposition performance of Pt/CTA. |
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ISSN: | 0888-5885 1520-5045 |
DOI: | 10.1021/acs.iecr.0c04568 |