Hydrothermal Annealing of Hierarchical ZSM‐5 Zeolites Improves Catalytic Performance

K Kumari Shilpa H Heng Dai (Department of Chemical and Biomolecular Engineering University of Houston Houston Texas TX 77204 USA) P Peng Lu (The ZeoMat Group, Key Laboratory of Photoelectric Conversion and Utilization of Solar Energy, Qingdao New Energy Shandong Laboratory) X Xinwei Ye C Carolin Rieg S Song Luo (Department of Chemical Engineering University of Massachusetts Amherst Massachusetts 01003 USA) H Han Chen (GBRCE for Functional Molecular Engineering, LIFM, IGCME, School of Chemistry) O Omar Abdelrahman (Department of Chemical and Biomolecular Engineering University of Houston Houston Texas TX 77204 USA) W Wei Fan (State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering) B Bert M. Weckhuysen (Inorganic Chemistry and Catalysis group, Institute for Sustainable and Circular Chemistry, Faculty of Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands) M Michael Tsapatsis (Department of Chemical and Biomolecular Engineering & Institute for NanoBioTechnology, Johns Hopkins University 2 , Baltimore, Maryland 21218-2625, and , Laurel, Maryland 20723,) J Jeffrey D. Rimer

Abstract

Abstract Engineering next‐generation zeolite catalysts requires state‐of‐the‐art synthesis techniques to tailor the properties of materials along with robust methods to evaluate their catalytic performance. Here, we introduce hydrothermal annealing as a facile and highly effective method to improve the activity and lifetime of zeolite catalysts. This post‐synthesis treatment uses a siliceous growth solution at approximate solubility of zeolite crystals with high temperature to alter the physicochemical properties of as‐synthesized materials. We employ the methanol‐to‐hydrocarbons (MTH) process as a benchmark reaction, along with a wide range of characterization techniques, to assess the impact of annealing on four nanosized and hierarchical ZSM‐5 materials compared to a commercial sample. Our findings reveal that annealing significantly increased cumulative MTH turnover without appreciably altering product selectivity, despite non‐obvious changes to zeolite structure as a result of the annealing process. Comparisons of catalyst performance are made under identical reaction conditions using a descriptor that correlates cumulative turnovers to compositional, mass transport, and textural properties of each material – in line with growing efforts to increase rigor and reproducibility in the field of catalysis. The collective approach used in this study serves as a guideline for establishing structure‐composition‐performance relationships for zeolite‐based catalysts across wide‐ranging applications.

Article Details

Volume / Issue Vol. 65, Issue 8
Published February 16, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

K

Kumari Shilpa

H

Heng Dai

Department of Chemical and Biomolecular Engineering University of Houston Houston Texas TX 77204 USA

P

Peng Lu

The ZeoMat Group, Key Laboratory of Photoelectric Conversion and Utilization of Solar Energy, Qingdao New Energy Shandong Laboratory

X

Xinwei Ye

C

Carolin Rieg

S

Song Luo

Department of Chemical Engineering University of Massachusetts Amherst Massachusetts 01003 USA

H

Han Chen

GBRCE for Functional Molecular Engineering, LIFM, IGCME, School of Chemistry

O

Omar Abdelrahman

Department of Chemical and Biomolecular Engineering University of Houston Houston Texas TX 77204 USA

W

Wei Fan

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering

B

Bert M. Weckhuysen

Inorganic Chemistry and Catalysis group, Institute for Sustainable and Circular Chemistry, Faculty of Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands

M

Michael Tsapatsis

Department of Chemical and Biomolecular Engineering & Institute for NanoBioTechnology, Johns Hopkins University 2 , Baltimore, Maryland 21218-2625, and , Laurel, Maryland 20723,

J

Jeffrey D. Rimer