Number of the records: 1
Reverse Micelles Directed Synthesis of TiO2-CeO2 Mixed Oxides and Investigation of Their Crystal Structure and Morphology
- 1.0386079 - ÚCHP 2013 RIV US eng J - Journal Article
Matějová, Lenka - Valeš, V. - Fajgar, Radek - Matěj, Z. - Holý, V. - Šolcová, Olga
Reverse Micelles Directed Synthesis of TiO2-CeO2 Mixed Oxides and Investigation of Their Crystal Structure and Morphology.
Journal of Solid State Chemistry. Roč. 198, FEB (2013), s. 485-495. ISSN 0022-4596. E-ISSN 1095-726X
R&D Projects: GA ČR GA203/09/1117; GA TA ČR TA01020804
Grant - others:GA ČR(CZ) GAP204/11/0785
Institutional support: RVO:67985858
Keywords : titania–ceria * cerium titanate * sol-gel preparation * reverse micelle * X-ray diffraction * Raman spectroscopy
Subject RIV: CI - Industrial Chemistry, Chemical Engineering
Impact factor: 2.200, year: 2013 ; AIS: 0.561, rok: 2013
DOI: https://doi.org/10.1016/j.jssc.2012.11.013
The synthesis of TiO2–CeO2 mixed oxides based on the sol–gel process controlled within reverse micelles of non-ionic surfactant Triton X-114 in cyclohexane is reported. The crystallization, phase composition, trends in nanoparticles growth and porous structure properties are studied as a function of Ti:Ce molar composition and annealing temperature by in-situ X-ray diffraction, Raman spectroscopy and physisorption. The brannerite-type CeTi2O6 crystallizes as a single crystalline phase at Ti:Ce molar composition of 70:30 and in the mixture with cubic CeO2 and anatase TiO2 for composition 50:50. At Ti:Ce molar ratios 90:10 and 30:70 the mixtures of TiO2 anatase, rutile and cubic CeO2 appear. In these mixtures TiO2 rutile is formed at higher temperatures than conventionally. Additionally, the amount of a present amorphous phase in individual mixtures was estimated from diffraction data. The porous structure morphology depends both on molar composition and annealing temperature. This is correlated with the presence of carbon impurities of different character.
Permanent Link: http://hdl.handle.net/11104/0219463
File Download Size Commentary Version Access 0386079.pdf 1 8.9 MB Author’s postprint open-access
Number of the records: 1