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FTIR Spectroscopic Study of Titanium-Containing Mesoporous Silicate Materials Научная публикация

Журнал Langmuir
ISSN: 0743-7463 , E-ISSN: 1520-5827
Вых. Данные Год: 2005, Том: 21, Номер: 23, Страницы: 10545-10554 Страниц : 10 DOI: 10.1021/la0514516
Ключевые слова MOLECULAR-SIEVES; THIOETHER OXIDATIONS; CATALYTIC-ACTIVITY; SURFACE-ACIDITY; TS-1 CATALYSTS; Ti(IV) CENTERS; Ti-SILICALITE; CO ADSORPTION; NH3; IR
Авторы Trukhan Natalia N. 1 , Panchenko Alexander A. 1 , Roduner Emil 1 , Mel'gunov Maxim S. 2 , Kholdeeva Oxana A. 2 , Mrowiec-Białoń Julita 3 , Jarzębski Andrzej B. 4
Организации
1 Institute of Physical Chemistry, Stuttgart University, Pfaffenwaldring 55, D-70569 Stuttgart, Germany
2 Boreskov Institute of Catalysis, Acad. Lavrentiev Av. 5, 630090 Novosibirsk, Russia
3 Institute of Chemical Engineering, Polish Academy of Sciences, Bałtycka 5, 44-100 Gliwice, Poland
4 Department of Chemical Engineering, Silesian University of Technology, M. Strzody 7, 44-100 Gliwice, Poland

Реферат: The surface acidity of different mesoporous titanium−silicates, such as well-organized hexagonally packed Ti−MMM, Ti−MMM-2, Ti−SBA-15, and amorphous TiO2−SiO2 mixed oxides (aerogels and xerogels), was studied by means of FTIR spectroscopy of CO adsorbed at 80 K and CD3CN adsorbed at 293 K. The surface hydroxyl groups of mesoporous titanium-silicates with 2−7 wt % Ti revealed a Brönsted acidity slightly higher to that of pure silicate. TiO2−SiO2 xerogels revealed the highest Brönsted acidity among the titanium−silicates studied. CO adsorption revealed two additional sites on the surface in comparison to pure silicate, characterized by ν(CO) from 2185 (high pressure) to 2178 (low pressure) cm-1 and from 2174 (high pressure) to 2170 (low pressure) cm-1. These bands are due to CO adsorbed on isolated titanium cations in the silica surrounding or having one Ti4+ cation in their second coordination sphere and due to CO interactions with Ti−OH groups, respectively. CD3CN adsorption similarly revealed the existence of two additional sites, which were not detected for pure silicate:  at 2289 cm-1 due to CD3CN interaction with titanol groups and from 2306 (low pressure) to 2300 (high pressure) cm-1 due to acetonitrile interaction with isolated framework titanium cations with probably one Ti4+ cation in their second coordination shell. The spectroscopic results are compared with computational data obtained on cluster models of titanium−silicate with different titanium content. According to the IR data, the Ti accessibility on the surfaces for mesoporous titanium−silicates with similar Ti loading (2 wt %) was found to fall in the order TiO2−SiO2 aerogel ∼ TiO2−SiO2 xerogel > Ti−MMM ∼ Ti−MMM-2 > Ti−SBA-15. This order (except TiO2−SiO2 xerogel) correlates with the catalytic activity found previously for titanium−silicates in 2,3,6-trimethylphenol oxidation with H2O2.
Библиографическая ссылка: Trukhan N.N. , Panchenko A.A. , Roduner E. , Mel'gunov M.S. , Kholdeeva O.A. , Mrowiec-Białoń J. , Jarzębski A.B.
FTIR Spectroscopic Study of Titanium-Containing Mesoporous Silicate Materials
Langmuir. 2005. V.21. N23. P.10545-10554. DOI: 10.1021/la0514516 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 2 июн. 2005 г.
Принята к публикации: 10 авг. 2005 г.
Опубликована online: 27 сент. 2005 г.
Опубликована в печати: 1 нояб. 2005 г.
Идентификаторы БД:
Web of science: WOS:000233129500051
Scopus: 2-s2.0-28044450410
РИНЦ: 13483437
Chemical Abstracts: 2005:1032311
Chemical Abstracts (print): 143:447510
OpenAlex: W2040581625
Цитирование в БД:
БД Цитирований
Web of science 42
Scopus 42
РИНЦ 42
OpenAlex 41
Альметрики: