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Synergistic effect for promoted benzene oxidation over monolithic CoMnAlO catalysts derived from in situ supported LDH film
[Display omitted] •Monolithic CoMnAl LDH films are prepared by ammonia hydrothermal growing on Al palte.•CoMnAlO film catalysts are obtained by the calcination of LDH precursor.•Structural and benzene oxidation of the film catalysts are well characterized.•CoMn2AlO shows best activity with T90 = 238...
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Published in: | Catalysis today 2019-07, Vol.332, p.132-138 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Monolithic CoMnAl LDH films are prepared by ammonia hydrothermal growing on Al palte.•CoMnAlO film catalysts are obtained by the calcination of LDH precursor.•Structural and benzene oxidation of the film catalysts are well characterized.•CoMn2AlO shows best activity with T90 = 238 °C at space velocity 300,000 ml g−1 h−1.•Synergistic effect promoted benzene degradation over monolithic CoMnAlO films.
Monolithic catalysts with high catalytic activity bring about increasing interest in practical environmental purification field for volatile organic compounds (VOCs) degradation with low pressure drops. Monolithic CoMnAlO catalysts with varied Co/Mn molar ratio derived from in situ supported layered double hydroxides (LDH) film are prepared through ammonia hydrothermal growing on Al substrate following calcinations. The textural properties for CoMnAlO catalysts with low temperature reducibility, surface element species are controlled by tuning the initial Co/Mn molar ratio verified through H2-TPR and XPS spectra. CoMn2AlO film sample shows best activity with the temperature for 90% benzene decomposition (T90) around 238 °C with space velocity 300,000 ml gcat−1 h−1. The reaction rate of CoMn2AlO film is about 1.32 mmol gcat−1 h−1 at 260 °C with T99, which is nearly two times to that of Co3AlO film catalyst with 0.73 mmol gcat−1 h−1, because of the higher Mn4+/Mn3+ and Co3+/Co2+ atomic ratios and reducibility inducing by the synergistic effect of Co and Mn. The value is five times higher than CoMn2AlO powder catalyst with 0.26 mmol gcat−1 h−1, which is due to the great exposure active sites. |
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ISSN: | 0920-5861 1873-4308 |
DOI: | 10.1016/j.cattod.2018.08.014 |