کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
66123 48416 2012 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Acid–base properties of TiO2-modified MCM-41 mesoporous silica and its catalytic performance for ortho-selective ethylation of phenol with diethyl carbonate
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
پیش نمایش صفحه اول مقاله
Acid–base properties of TiO2-modified MCM-41 mesoporous silica and its catalytic performance for ortho-selective ethylation of phenol with diethyl carbonate
چکیده انگلیسی

A series of catalysts were prepared by impregnation of MCM-41 mesoporous silica with TiO2. Alkylation of phenol with diethyl carbonate was carried out over the TiO2-modified MCM-41 catalysts for the first time, and the reaction had high ortho-selectivity and a high phenol conversion. The physicochemical properties of the catalysts were characterized by X-ray diffraction, X-ray fluorescence, N2 adsorption–desorption, Fourier-transform infrared spectroscopy with pyridine adsorption, and CO2 and NH3 temperature programmed desorption. Long-range regularity of the hexagonal arrays of MCM-41 was sustained after TiO2 modification. As the TiO2 mass fraction in the catalyst increased, the number of acidic and basic sites also increased, which suggests that TiO2 modification affects the acid–base properties of MCM-41. The high ortho-selectivity and the high phenol conversion for alkylation of phenol with diethyl carbonate over TiO2-modified MCM-41 could be ascribed to catalytic interaction between adjacent acidic and basic sites on the catalysts. The effects of temperature, feed ratio, reactant contact time and time-on-stream on the conversion of phenol and the selectivity for various products over TiO2-modified MCM-41 catalysts were also investigated.

Figure optionsDownload high-quality image (112 K)Download as PowerPoint slideHighlights
► Acid–base properties of the TiO2 modified MCM-41 has been studied.
► High ortho-selectivity is obtained for alkylation of phenol with diethyl carbonate.
► Catalytic interaction between acidic sites and basic sites is approved.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Catalysis A: Chemical - Volume 357, May 2012, Pages 50–58
نویسندگان
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