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Tetrapropylammonium Hydroxide Treatment of Aged Dry Gel to Make Hierarchical TS-1 Zeolites for Catalysis

[Image: see text] This work presents the development and systematic study of a method to prepare hierarchical titanium silicalite-1 (TS-1) zeolites with high tetra-coordinated framework Ti species content. The new method involves (i) the synthesis of the aged dry gel by treating the zeolite precurso...

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Detalles Bibliográficos
Autores principales: Yang, Zhenyuan, Guan, Yanan, Xu, Lei, Zhou, Yangtao, Fan, Xiaolei, Jiao, Yilai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983304/
https://www.ncbi.nlm.nih.gov/pubmed/36879771
http://dx.doi.org/10.1021/acs.cgd.2c01291
Descripción
Sumario:[Image: see text] This work presents the development and systematic study of a method to prepare hierarchical titanium silicalite-1 (TS-1) zeolites with high tetra-coordinated framework Ti species content. The new method involves (i) the synthesis of the aged dry gel by treating the zeolite precursor at 90 °C for 24 h; and (ii) the synthesis of hierarchical TS-1 by treating the aged dry gel using tetrapropylammonium hydroxide (TPAOH) solution under hydrothermal conditions. Systematic studies were conducted to understand the effect of the synthesis conditions (including the TPAOH concentration, liquid-to-solid ratio, and treatment time) on the physiochemical properties of the resulting TS-1 zeolites, and the results showed that the condition of a TPAOH concentration of 0.1 M, liquid-to-solid ratio of 1.0, and treatment time of 9 h was ideal to enable the synthesis of hierarchical TS-1 with a Si/Ti ratio of 44. Importantly, the aged dry gel was beneficial to the quick crystallization of zeolite and assembly of nanosized TS-1 crystals with a hierarchical structure (S(ext) = 315 m(2) g(–1) and V(meso) = 0.70 cm(3) g(–1), respectively) and high framework Ti Species content, making the accessible active sites ready for promoting oxidation catalysis.