Number of the records: 1  

Catalytic and photocatalytic processes on 18O-labeled TiO2

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    SYSNO ASEP0369217
    Document TypeC - Proceedings Paper (int. conf.)
    R&D Document TypeConference Paper
    TitleCatalytic and photocatalytic processes on 18O-labeled TiO2
    Author(s) Kavan, Ladislav (UFCH-W) RID, ORCID
    Zukalová, Markéta (UFCH-W) RID, SAI, ORCID
    Ferus, Martin (UFCH-W) ORCID, RID
    Kürti, J. (HU)
    Koltai, J. (HU)
    Civiš, Svatopluk (UFCH-W) RID, ORCID, SAI
    Source TitleSborník příspěvků. 5. Seminář výzkumného centra NANOPIN. Nanomateriály a fotokatalýza. - Praha : VŠCHT Praha, 2011 / Krýsa J. ; Klusoň P. - ISBN 978-80-7080-780-4
    Pagess. 11-13
    Number of pages3 s.
    ActionSeminář výzkumného centra NANOPIN. Nanomateriály a fotokatalýza /5./
    Event date20.06.2011-23.06.2011
    VEvent locationHnanice
    CountryCZ - Czech Republic
    Event typeWRD
    Languageeng - English
    CountryCZ - Czech Republic
    KeywordsTiO2 ; photocatalysis
    Subject RIVCG - Electrochemistry
    R&D Projects1M0577 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    Annotation18O-isotope labelled titania (anatase, rutile) was synthesized. The products were characterized by Raman spectra together with their quantum chemical modelling. The interaction with carbon dioxide was investigated using high-resolution FTIR spectroscopy, in dark and upon UV-excitation. The oxygen isotope exchange at the Ti18O2/C16O2 interface was elucidated. The C18O2 was formed as the dominating final product with a minor content of C16O18O. The rate of oxygen-isotope exchange is highly sensitive to the conditions of the titania pretreatment. The vacuum-annealed Ti18O2 at 450 C exhibited a very high spontaneous oxygen exchange activity with gaseous C16O2. A mechanism for the 18O/16O exchange process is discussed at the molecular level. The photocatalytic formation of methane, acetylene and C16O released from the Ti18O2 surface was triggered by an XeCl excimer laser irradiation.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2012
Number of the records: 1  

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