Organic‐Free Synthesis of Zeolite Y with High Si/Al Ratios: Combined Strategy of In Situ Hydroxyl Radical Assistance and Post‐Synthesis Treatment

Author:

Wang Jianyu1ORCID,Liu Pusheng12,Boronat Mercedes3ORCID,Ferri Pau3ORCID,Xu Zhaoguo1,Liu Peng4,Shen Baojian4,Wang Zhendong5,Yu Jihong16ORCID

Affiliation:

1. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P. R. China

2. Lanzhou Petrochemical Research Center PetroChina Lanzhou 730060 P. R. China

3. Instituto de Tecnologia Quimica Universitat Politecnica de Valencia Consejo Superior de Investigaciones Cientificas 46022 Valencia Spain

4. State Key Laboratory of Heavy Oil Processing The Key Laboratory of Catalysis of CNPC College of Chemical Engineering China University of Petroleum Beijing 102249 P. R. China

5. Sinopec Shanghai Research Institute of Petrochemical Technology State Key Laboratory of Green Chemical Engineering and Industrial Catalysis Shanghai 201208 P. R. China

6. International Center of Future Science Jilin University Changchun 130012 P. R. China

Abstract

AbstractZeolite Y, with a high SiO2/Al2O3 ratio (SAR), plays an important role in fluidized catalytic cracking processes. However, in situ synthesis of zeolite Y with high SARs remains a challenge because of kinetic limitations. Here, zeolite Y with an SAR of 6.35 is synthesized by a hydroxyl radical assisted route. Density‐functional theory (DFT) calculations suggest that hydroxyl radicals preferentially enhanced the formation of Si‐O‐Si bonds, thus leading to an increased SAR. To further increase the SAR, a dealumination process was carried out using citric acid, with a subsequent second‐step hydrothermal crystallization, giving an SAR of up to 7.5 while maintaining good crystallinity and high product yield. The resultant zeolite Y shows good performance in cumene cracking. Introduced here is a new strategy for synthesizing high SAR zeolite Y, which is widely used in commercial applications.

Funder

National Natural Science Foundation of China

National Basic Research Program of China

Higher Education Discipline Innovation Project

Publisher

Wiley

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