Gloria Issa, Martin Kormunda, Momtchil Dimitrov, Jiri Henych, Radostina Ivanova and Tanya Tsoncheva
University of Jan Evangelista Purkyne, Czechia
Bulgarian Academy of Sciences, Sofia, Bulgaria
Institute of Inorganic Chemistry AS CR v.v.i., Czechia
Posters & Accepted Abstracts: J Material Sci Eng
Current investigation is aimed at the investigation of the textural, structural, redox and catalytic properties of
MnTi binary oxides in comparison with their single analogues. Template assisted hydrothermal technique
was used for the preparation of xMnyTi mixed oxides, varrying the x/y ratio in a wide range. A complex of
different physicochemical techniques, such as nitrogen physisorption, XRD, TPR, UV-Vis, FTIR, Raman, SEM
and XPS spectroscopies, were applied for their characterization. The catalytic behaviour was studied in methanol
decomposition to CO and hydrogen as a potential alternative fuel. All prepared materials exhibited high surface area
and mesoporous volume. Among them, the binary oxides demonstrated improved textural characteristics, which
was most pronounced for 5Mn5Ti. XRD and Raman analyses showed co-existence of anatase, Mn2O3, Mn5O8 and
Mn3O4 for 2Mn8Ti and 8Mn2Ti and well crystallized anatase and rutile for 5Mn5Ti, which were also better dispersed
as compared to the single oxides. The slight changes in the anatase unit cell parameters for the binary materials did
not exclude partial isomorphous substitution of Ti4+ by Mnn+ ions. XPS analyses showed stabilization if Ti and Mn
ions in lower oxidative state. TPR-TG experiments demonstrated improved reducibility of the mixed oxide samples
as compared to their single analogues. This could be due to the improved dispersion and formation of more labile
shared Mn-O-Ti bonds. It was found that small manganese additives to titania promoted the catalytic activity in
methanol decomposition but this effect could be controlled by the x/y ratio in the mixed oxides.
Acknowledgement: The authors from IOCCP, BAS thank the project DFNI H29/3/28.08.2018 for the financial
support during the preparation of the materials and catalytic tests and bilateral project BAS- AS CR for the help
in physicochemical characterization. The authors thank the project CZ.02.2.69/0.0/0.0/16_027/0008492 for the
financial support.
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