Characterization of 12-molybdophosphoric acid supported on mesoporous silica MCM-41 and its catalytic performance in the synthesis of hydroquinone diacetate

被引:36
|
作者
Ahmed, Awad I. [1 ]
Samra, S. E. [1 ]
El-Hakam, S. A. [1 ]
Khder, A. S. [2 ]
El-Shenawy, H. Z. [1 ]
El-Yazeed, W. S. Abo [1 ]
机构
[1] Mansoura Univ, Fac Sci, Dept Chem, Mansoura, Egypt
[2] Umm Al Qura Univ, Fac Sci Appl, Mecca, Saudi Arabia
关键词
MCM-41; Surface area; Surface acidity; Hydroquinone diacetate; N-PENTANE ISOMERIZATION; HETEROPOLY ACIDS; MOLECULAR-SIEVES; EFFICIENT CATALYST; ZIRCONIA; SURFACE; OXIDE; NANOPARTICLES; ALKYLATION; REACTIVITY;
D O I
10.1016/j.apsusc.2013.05.105
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
12-molybdophosphoric acid (PMA) was supported on mesoporous molecular sieves MCM-41 by impregnation of 12-molybdophosphoric acid followed by calcination. The nanochannels of MCM-41 provide a large surface area for the solid state dispersion of 12-molybdophosphoric acid. The samples have been characterized by N-2 adsorption-desorption at -196 degrees C, transmission electron microscopy (TEM), powder X-ray diffraction (PXRD), and FT-IR measurements. The acidity and catalytic activity have been, respectively, examined by nonaqueous titration of n-butylamine in acetonitrile and synthesis of hydroquinone diacetate. The results showed that ordered hexagonal pore structure was observed in the synthesized MCM-41. Also the results indicate that PMA are highly dispersed on mesoporous silica MCM-41 spherical nanoparticles while PMA retains its Keggin structure. On the other hand, with increasing the introduced PMA amount, the specific surface area decreases, and the mesoporous ordering of the samples become poor. Both the surface acidity and the catalytic activity sharply increase with the modification of MCM-41 by PMA but decrease by increasing the calcination temperature. The sample with 55 wt% PMA/MCM-41 calcined at 350 degrees C shows the highest acidity and catalytic activity. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:217 / 225
页数:9
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