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A Titanium Silicalite-1 (TS-1) Catalyst with Abundant Active Ti-VI Species for Efficient Conversion of Ethylene to
Huali Tan1, Yi Zuo1, Gudan Li1
1State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials Oriented Chemical Engineering, School of Chemical Engineering, Dalian University of Technology, No. 2 Linggong Road, Dalian, 116024, China.
Abstract:
One-pot synthesis of glycol from ethylene and H2O2 is simple and environmentally friendly, making it a potential alternative for glycol production. The key to the success of this is to have a bifunctional catalyst with both oxidative activity for ethylene epoxidation and acidic centers for the hydration of ethylene oxide. Typically, the incorporation of trivalent metal ions into titanium silicalite-1 (TS-1) framework can provide the two types of active centers, but this often results in decreased oxidative activity. Here, we propose a dual-chemical post-treatment regime to introduce acid centers in TS-1 while simultaneously improving oxidative activity. The combined tetrapropylammonium hydroxide (TPAOH) + (NH4)2CO3 post-treatment not only produces abundant Ti(OSi)2(OH)4 (Ti-VI) species from Ti(OSi)4, but also creates internal cavities within TS-1. Ti-VI possesses both high oxidative activity and acidic sites. The presence of internal cavities enhances the diffusion on the catalyst as well as increases the accessibility of Ti-VI species. Consequently, when applied as a catalyst, the combined-treated TS-1 demonstrates an outstanding catalytic performance, achieving 98.6 % conversion of H2O2 and 99.8 % selectivity of EG, which is ≈2 times of the conventional TS-1. This study also unveils the formation mechanism of Ti-VI during the post-treatment.
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