共聚物
介孔材料
化学工程
结晶
材料科学
催化作用
微球
微晶
吡啶
纳米颗粒
高分子化学
化学
纳米技术
有机化学
聚合物
复合材料
工程类
冶金
作者
Zhendong Wang,Le Xu,Jingang Jiang,Yueming Liu,Mingyuan He,Peng Wu
标识
DOI:10.1016/j.micromeso.2012.02.025
摘要
Mesoporous TS-1 microspheres, denoted as M-TS-1-MS, were directly synthesized by adding triblock copolymer (F127 or P123) into the synthetic system for crystallizing conventional TS-1 (C-TS-1). With the assistance of surfactant, TS-1 nanoparticles of 50–100 nm were self-assembled into microspheres which contained regular intercrystal mesopores in the range of 6–10 nm in addition to original micropores. The crystallite aggregates in microspheres did not collapse after ultrasonication for 2 h or refluxing in 2 M HNO3 for 20 h. The high mechanical strength implied their potential applications in slurry reactors where an easy separation of solid catalyst from reaction mixture is required. M-TS-1-MS was comparably active to C-TS-1 in pyridine oxidation and 1-hexene epoxidation with H2O2 as the oxidant, whereas exhibited a higher activity in the oxidation of bulky substrates such as 3-picoline and cyclohexene due to the presence of mesopores. By tracking the crystallization process at different stages, a tentative mechanism is proposed to explain the role of triblock copolymer in inducing the aggregation of nanocrystals to microspheres.
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