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Ruthenium versus Platinum on Cerium Materials in Wet Air Oxidation of Acetic Acid.
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SYSNO ASEP 0469246 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Ruthenium versus Platinum on Cerium Materials in Wet Air Oxidation of Acetic Acid. Tvůrce(i) Gaálová, Jana (UCHP-M) RID, SAI, ORCID
Barbier, Jr., J. (FR)
Rossignol, S. (FR)Zdroj.dok. Journal of Hazardous Materials. - : Elsevier - ISSN 0304-3894
Roč. 181, 1-3 (2010), s. 633-639Poč.str. 7 s. Jazyk dok. eng - angličtina Země vyd. NL - Nizozemsko Klíč. slova ruthenium ; ceria ; deactivation Vědní obor RIV CC - Organická chemie Institucionální podpora UCHP-M - RVO:67985858 UT WOS 000280601300083 EID SCOPUS 77954564948 DOI https://doi.org/10.1016/j.jhazmat.2010.05.059 Anotace This study was a comparison between Ru-catalysts and similar, previously investigated, Pt-catalysts. In this paper, ruthenium catalysts for catalytic wet air oxidation are prepared, characterized and tested. Both catalysts were supported on commercial CeO2 as well as mixed oxide Zr0.1(Ce0.75Pr0.25)0.9O2. The catalysts were characterized by measuring the oxygen storage capacities (OSC), BET, XRD, FTIR and chemisorption of hydrogen. In addition, the effect of sintering (treatments under H2) was compared with both of the catalysts. The comparison of the results showed that initial intrinsic activity of ruthenium is not significantly influenced by the type of the support, which is contrast to platinum. Furthermore, the particle size of Ru had an important effect on CWAO activity: the higher the particle size, the better the activity. This was different with Pt-catalysts, where the optimal particle size was smaller, having about 15% of metal dispersion. Pracoviště Ústav chemických procesů Kontakt Eva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227 Rok sběru 2017
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