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Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
Preparation of Hierarchical Ti-Sil-BEA Zeolite by Silanization Modification for the Application in Dicyclopentadiene
Tianzeng Zhao1, Xinxin Peng1, Zhongpeng Zhu1
1SINOPEC Research Institute of Petroleum Processing Co.,Ltd., No. 18 Xueyuan Road, Haidian District, Beijing 100083, China.
Abstract:
The pore-expanding modification of zeolites is an important means to improve their catalytic performance. This study demonstrates the postsynthesis of Ti-Sil-BEA zeolites via silanization-modified parent BEA zeolite and its application in catalyzing epoxidation reactions of dicyclopentadiene (DCPD). The zeolites were characterized by BET, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, UV-vis spectroscopy, and X-ray electron spectroscopy. The impact of silanizing reagents on the crystallization of BEA zeolites as well as pore-expanding was studied. It is revealed that the addition of N-[3-(Trimethoxysilyl)-propyl]-ethylenediamine (TSPED) before crystallization of *BEA-type zeolites can effectively introduce mesoporous structures without impacting the integrity of the zeolite crystals (resulting in an augmentation of the mesopore volume by 55% and emergence of mesopores with a diameter of 11 nm). Furthermore, the introduction of TSPED led to the reduction of zeolite size, and the change of the mesoporous structure of Ti-Sil-BEA improved its catalytic performance for the DCPD epoxidation reaction; the DCPD conversion was increased by 11.5%. The dicyclopentadiene dioxide (DCPDDO) selectivity was increased by 52.5%.
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