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On thermal stability and catalytic reactivity of Zr-metal-organic framework (UiO-67) encapsulated Pt catalysts

机译:Zr-金属 - 有机骨架(UiO-67)包覆pt催化剂的热稳定性和催化活性

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摘要

Pt nanoparticles (NPs, 0.5 wt.%) encapsulated in a zirconium-based metal-organic framework (UiO-67 MOF) were synthesised via a linker design method. Thermal behaviours of Pt in UiO-67 composite materials were studied using thermogravimetric and differential thermal analysis (TG-DTA) in comparison with UiO-67. TG-DTA results showed that Pt insertion can impair the thermal stability of the bulk UiO-67 resulting in a ca. 14% drop in the critical temperature of the thermal decomposition. Temperature-programmed oxidation of materials showed that calcination at 450 K was essential to render a clean framework. Temperature-programmed reduction of materials revealed that the chemisorption of H2 on UiO-67 (at 323 K) was evidently enhanced owing to the incorporation of Pt NPs thus making PtNP@UiO-67 suitable for hydrogenation reactions and hydrogen storage. PtNP@UiO-67 catalyst was evaluated by the oxidation and hydrogenation of 5-hydroxymethylfurfural in aqueous solutions at 363 K showing an improved activity and selectivity in hydrogenation reactions.
机译:通过接头设计方法合成了封装在锆基金属有机骨架(UiO-67 MOF)中的Pt纳米颗粒(NPs,0.5 wt。%)。与UiO-67相比,使用热重分析和差热分析(​​TG-DTA)研究了Pt在UiO-67复合材料中的热行为。 TG-DTA结果表明,Pt的插入会损害块状UiO-67的热稳定性,从而产生约5%的热稳定性。热分解的临界温度下降14%。材料的程序升温氧化表明,在450 K下煅烧对于提供干净的骨架至关重要。程序升温还原的材料表明,由于引入了Pt NP,H2在UiO-67(在323 K)上的化学吸附明显增强,因此使PtNP @ UiO-67适用于氢化反应和储氢。 PtNP @ UiO-67催化剂是通过在水溶液中于363 K下对5-羟甲基糠醛进行氧化和氢化来评估的,显示出改进的氢化反应活性和选择性。

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