Rapid Synthesis of ZSM-50 Zeolites for Effective <i>n</i>-Heptane Hydroisomerization

In this study, a rapid synthesis of ZSM-50 zeolites is achieved by a two-step aging–crystallization hydrothermal method. By optimizing the temperature/time for aging (393 K/48 h) and crystallization (423 K/72 h), the synthesis time for obtaining pure-phase ZSM-50 zeolites has been significantly shortened to 4 days from typically weeks. The gel compositions to form pure-phase ZSM-50 have also been mapped out in the ternary composition diagram of 5Al2O3/SiO2–OSDA/SiO2–OH–/SiO2 under the optimized aging–crystallization conditions. Furthermore, three ZSM-50 samples are synthesized using different gel compositions and/or crystallization conditions. The samples have different acidity characteristics and average crystal sizes from 5 to 17 μm. As catalysts for n-heptane hydroisomerization, the three Pt-loaded ZSM-50 catalysts deliver the maximum iso-heptane yield directly correlated to their surface weak Brönsted acid sites on the external surface. The ZSM-50 (5 μm) catalyst has a superior catalytic activity, achieving a maximum iso-heptane yield of 71.4% at 543 K, along with a high fraction of multibranched isomers of 29.1%. This study highlights the pivotal role of particle size in modulating acid properties and pore accessibility in ZSM-50 and offers a facile strategy for designing effective bifunctional catalysts for n-alkane isomerization.

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Publication Details

Journal
Chemistry of Materials
Published
2025-08-14
DOI
https://doi.org/10.1021/acs.chemmater.5c00735
Citations
1
Primary Topic
Geochemistry and Geologic Mapping
Type
article
Field-Weighted Citation Impact
2.48
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article

Rapid Synthesis of ZSM-50 Zeolites for Effective n-Heptane Hydroisomerization

1 citations
Chemistry of Materials
Geochemistry and Geologic Mapping
2.48
article

Rapid Synthesis of ZSM-50 Zeolites for Effective n-Heptane Hydroisomerization

article en
1 citations

Abstract

In this study, a rapid synthesis of ZSM-50 zeolites is achieved by a two-step aging–crystallization hydrothermal method. By optimizing the temperature/time for aging (393 K/48 h) and crystallization (423 K/72 h), the synthesis time for obtaining pure-phase ZSM-50 zeolites has been significantly shortened to 4 days from typically weeks. The gel compositions to form pure-phase ZSM-50 have also been mapped out in the ternary composition diagram of 5Al2O3/SiO2–OSDA/SiO2–OH–/SiO2 under the optimized aging–crystallization conditions. Furthermore, three ZSM-50 samples are synthesized using different gel compositions and/or crystallization conditions. The samples have different acidity characteristics and average crystal sizes from 5 to 17 μm. As catalysts for n-heptane hydroisomerization, the three Pt-loaded ZSM-50 catalysts deliver the maximum iso-heptane yield directly correlated to their surface weak Brönsted acid sites on the external surface. The ZSM-50 (5 μm) catalyst has a superior catalytic activity, achieving a maximum iso-heptane yield of 71.4% at 543 K, along with a high fraction of multibranched isomers of 29.1%. This study highlights the pivotal role of particle size in modulating acid properties and pore accessibility in ZSM-50 and offers a facile strategy for designing effective bifunctional catalysts for n-alkane isomerization.

Chemistry of MaterialsVol. 37(16)
Sinopec (China) (CN), The University of Western Australia (AU), Dalian University of Technology (CN), Smart Material (Germany) (DE), State Key Laboratory of Fine Chemicals
Clean water and sanitation
Openalex Percentile: Top 7%
Geochemistry and Geologic Mapping
2.48
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