Enhanced catalytic activity of Pt/H-ZSM-12 via alkaline post-treatment for the hydroisomerization of n-hexane

Bifunctional Pt/H-ZSM-12 catalysts with enhanced inter-mesoporosity were prepared from synthesized ZSM-12 samples by alkaline post-treatments with or without the presence of the template in the zeolite pores, ammonium ion-exchange, and impregnation with Pt(NH3)4Cl2. Different techniques, such as N2...

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Veröffentlicht in:Microporous and mesoporous materials 2020-10, Vol.306, p.110459, Article 110459
Hauptverfasser: Lu, Xinqing, Guo, Yuping, Zhang, Yang, Ma, Rui, Fu, Yanghe, Zhu, Weidong
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Sprache:eng
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Zusammenfassung:Bifunctional Pt/H-ZSM-12 catalysts with enhanced inter-mesoporosity were prepared from synthesized ZSM-12 samples by alkaline post-treatments with or without the presence of the template in the zeolite pores, ammonium ion-exchange, and impregnation with Pt(NH3)4Cl2. Different techniques, such as N2 adsorption-desorption, X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), NH3 temperature-programmed desorption (NH3-TPD), and pyridine-adsorption infra-red spectroscopy (Py-IR), were used to characterize the synthesized samples. The prepared Pt/H-ZSM-12 catalysts were evaluated in the hydroisomerization of n-hexane. The results show that the template-containing ZSM-12 is a better parent for introducing abundant inter-mesopores by the alkaline post-treatment, accompanying with a better preservation of microporosity and strong acid sites, in comparison to the template-free ZSM-12 as the parent. In addition, the dispersion of Pt on the alkaline-treated zeolite is increased as well, which is also helpful to enhance the conversion of n-hexane and the selectivity for the dibranched hexanes. [Display omitted] •Introduced inter-mesoporosity in templated ZSM-12 with alkaline treatment.•Microporosity and acidity well preserved in the alkali-treated ZSM-12.•Introduced mesoporosity helps the dispersion of Pt on the zeolite.•Introduced mesoporosity enhances the hydroisomerization performance.
ISSN:1387-1811
1873-3093
DOI:10.1016/j.micromeso.2020.110459