结晶
钛
沸石
苯酚
催化作用
分子筛
化学工程
羟基化
溴化物
水热合成
扩散
化学
材料科学
热液循环
无机化学
核化学
有机化学
工程类
酶
物理
热力学
作者
Yi Zuo,Yu Chen,Tonghui Li,Jiaojiao Yu,Hong Yang,Min Liu,Xinwen Guo
标识
DOI:10.1016/j.micromeso.2022.111884
摘要
A bulky composite material, CaCO3@TS-1, was synthesized in a tetrapropylammonium bromide hydrothermal system by adding nanosized CaCO3 particles of 60–80 nm to a titanium silicalite-1 (TS-1) synthesis gel. The macroporous TS-1 free of extraframework Ti was then obtained by the posttreatment of the CaCO3@TS-1 in HCl solution to remove CaCO3 and extraframework Ti simultaneously. This study demonstrates that this new synthesis route, the acidity posttreatment, can produce a bulky TS-1 with volume-controllable intracrystal macropores. The crystallization mechanism of the macroporous TS-1 was studied systematically. The addition of CaCO3 accelerates the crystallization of silicon source, and leads to the similar crystallization rates of silicon and titanium sources. Therefore, the formation of extraframework Ti was inhibited, and more Ti ions were inserted into the TS-1 framework. The catalytic performance of macroporous TS-1 was evaluated in the hydroxylation of phenol. An outstanding catalytic activity was obtained due to their enhanced diffusion property and reduced extraframework Ti.
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