Volume 48, Issue 5 e70023
Research Article

Pore Size Effects over Hierarchical Pore Hβ via Two-Stage Crystallization in Benzene Hydroalkylation

Zhang Liangliang

Zhang Liangliang

School of Petrochemical Engineering, Liaoning Petrochemical University, No. 1 West Section of Dandong Road, Fushun, Liaoning, 113001 China

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Cai Yulin

Cai Yulin

School of Petrochemical Engineering, Liaoning Petrochemical University, No. 1 West Section of Dandong Road, Fushun, Liaoning, 113001 China

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Dr. Han Qiao

Corresponding Author

Dr. Han Qiao

School of Petrochemical Engineering, Liaoning Petrochemical University, No. 1 West Section of Dandong Road, Fushun, Liaoning, 113001 China

E-mail: [email protected]; [email protected]

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He Jing

He Jing

Hebei Marketing Company of PetroChina Co., Ltd., Quality Testing Center, No. 9 Shiqing Road, Shijiazhuang, Hebei, 050000 China

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Prof. Dr. Sun Na

Corresponding Author

Prof. Dr. Sun Na

School of Petrochemical Engineering, Liaoning Petrochemical University, No. 1 West Section of Dandong Road, Fushun, Liaoning, 113001 China

E-mail: [email protected]; [email protected]

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First published: 15 April 2025

Abstract

Hierarchical pore Hβ molecular sieve with high crystallinity were synthesized by two-step hydrothermal crystallization and seed-assisted, indicating that the method was more favorable to synthesize the hierarchical pore structure, and seed-assisted was helpful to improve the relative crystallinity and acid properties of Hβ. Compared with microporous Hβ, the hierarchical pore Hβ synthesized by a two-step hydrothermal crystallization strategy were presented high performance of benzene hydroalkylation. The conversion of benzene was 54.69 %, selectivity for cyclohexylbenzene was 74.31 %, and the catalyst activities was relatively stable within 280 h under hydrogen pressure of 2 MPa, temperature of 473 K, liquid space speed of 1 h−1, and H2/benzene molar ratio of 0.8 over Hβ loading 0.2 % (wt.%) Ru. Furthermore, the mesoporous structure of sample was beneficial to improve the diffusion rate of reactants and products and exposed more acidic active centers, which was conducive to the efficient hydroalkylation.

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