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Combustion of toluene over cobalt-modified MFI zeolite dispersed on monolith produced using 3D printing technique

期刊

CATALYSIS TODAY
卷 375, 期 -, 页码 369-376

出版社

ELSEVIER
DOI: 10.1016/j.cattod.2020.04.005

关键词

Total oxidation; Volatile organic compounds; Cobalt-containing catalysts; MFI zeolite; Monolith; 3D printing

资金

  1. Polish National Science Centre [2016/23/B/ST5/01108]
  2. European Regional Development Fund in the framework of the Polish Innovation Economy Operational Program [POIG.02.01.0012-023/08]

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A facile method using 3D printing to fabricate ceramic monoliths for Co3O4-based catalysts of total oxidation of volatile organic compounds was developed. The monoliths, coated with a MFI zeolite layer, showed excellent catalytic activity in toluene combustion due to highly dispersed Co3O4 spinel particles. The stability tests confirmed the longevity and consistent performance of the monolith catalysts in prolonged reactions.
A facile method of fabrication of ceramic monoliths assisted by 3D printing was developed for preparation of Co3O4-based catalysts of total oxidation of volatile organic compounds. The proposed approach was based on the production of a resin template, which was subsequently used at a casting step for the construction of corundum monolith. The walls of this material were additionally coated with a MFI zeolite layer providing the possibility of modification with a Co3O4 precursor using ion-exchange and impregnation techniques. The parent and Co3O4-modified monoliths with varying active phase content were characterized by SEM/EDS, XRD, XRF, XPS, UV-visDR and H-2-TPR. Their catalytic performance in the toluene combustion was also tested. It was shown that the formation of Co3O4 spinel particles highly dispersed on the zeolite-coated monolith resulted in excellent catalytic activity measured by very high TOF values. Furthermore, stability tests confirmed that the obtained monolith catalysts can work for prolonged reaction time without noticeable changes in the toluene conversion and selectivity to CO2.

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