A supported nickel-based catalyst for the selective hydrogenation of biomass derivatives, a method of preparation and use

By using PMSQ microsphere-supported nickel-based catalysts, the problems of hydrothermal stability and weak metal-support interaction in the selective hydrogenation reaction of biomass derivatives by traditional supports have been solved, realizing a highly efficient and selective hydrogenation reaction with bio-based alcohols as products, which is suitable for a variety of reaction media.

CN122399897APending Publication Date: 2026-07-17ZHEJIANG UNIV
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
ZHEJIANG UNIV
Filing Date
2026-05-09
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing γ-Al2O3 and SiO2 supports suffer from poor hydrothermal stability or weak metal-support interactions in the selective hydrogenation of biomass derivatives, leading to rapid catalyst deactivation and low conversion rates, which fail to meet the economic requirements of industrial production.

Method used

Using polymethylsilsesquioxane (PMSQ) microspheres as a support, metallic nickel is uniformly loaded through a vacuum freeze-drying process to form a core-shell structured supported nickel-based catalyst. Combined with a specific preparation method, the catalyst is ensured to have both hydrophilic and oleophilic wetting properties and high-temperature stability.

Benefits of technology

It achieves highly selective and active hydrogenation reactions of biomass derivatives in different reaction media, producing bio-based alcohols such as cyclopentanol and tetrahydrofurfuryl alcohol. It has both broad-spectrum media adaptability and excellent stability, and is suitable for aqueous phase, polar organic solvent phase or non-polar organic solvent phase.

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Abstract

本公开提供了一种用于生物质衍生物选择性加氢的负载型镍基催化剂、制备方法及应用,所述催化剂包括聚甲基硅倍半氧烷微球载体以及负载在所述载体上的金属镍活性组分;所述应用包括:在氢气存在下,于水相、极性有机溶剂相或非极性有机溶剂相中,使所述生物质衍生物与所述催化剂接触进行选择性加氢反应。金属镍与PMSQ载体之间形成Ni‑O‑Si界面键合结构,使催化剂由PMSQ本身的强疏水性转变为亲水亲油双亲性,从而能够在水相、极性有机相及非极性有机相中均实现生物质衍生物的高效选择性加氢。该催化剂具有优异的水热稳定性和热稳定性,用于生物质衍生物选择性加氢反应时可实现完全转化及较高的醇类选择性。
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