Boosting Acidity of SAPO-11 through Silicon Source Regulation: Towards High-Performance Ni-Based Catalysts for n-Dodecane Hydroisomerization

Abstract

SAPO-11 molecular sieves represent one of the most widely studied catalytic supports for alkane hydroisomerization in the petrochemical and coal chemical industries. Herein, we prepared a series of SAPO-11 samples by adjusting the addition amount of the silicon precursor during hydrothermal synthesis. The results demonstrate that the S11-0.25 sample achieves a maximum acid density of 903 μmol g-1 at a SiO2/Al2O3 molar ratio of 0.25. Combined NH3-TPD and 29Si-NMR characterizations confirm that isolated Si sites and minor silicon islands contribute to the enhancement of total acid content and acid strength. Subsequently, the optimized Ni/S11-0.25 catalyst with 4 wt% Ni loading was prepared via impregnation and evaluated for n‑dodecane hydroisomerization. This catalyst exhibits excellent isomerization selectivity together with a maximum iso-dodecane yield of 81.1%. The obtained results provide valuable references for the rational design of low‑cost non‑noble metal hydroisomerization catalysts.

Supplementary files

Article information

Article type
Paper
Submitted
18 Dec 2025
Accepted
09 Jun 2026
First published
10 Jun 2026

New J. Chem., 2026, Accepted Manuscript

Boosting Acidity of SAPO-11 through Silicon Source Regulation: Towards High-Performance Ni-Based Catalysts for n-Dodecane Hydroisomerization

S. Yang, J. Huang, W. Wang, H. Xu, H. Gao, S. Chen, B. Li and Z. Hua, New J. Chem., 2026, Accepted Manuscript , DOI: 10.1039/D5NJ04887G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements