Catalytic combustion of toluene over highly dispersed Pt NPs embedded in porous TiO2 via in situ pyrolysis of MOFs

被引：4

作者：

Yang, Jinping ^{[1
]}

Jiang, Yunpeng ^{[1
]}

Chu, Peiqi ^{[1
]}

Lv, Likang ^{[1
]}

Tao, Jinxiong ^{[1
]}

Wang, Zhiwei ^{[1
]}

Liu, Yuxi ^{[1
]}

Dai, Hongxing ^{[1
]}

Deng, Jiguang ^{[1
]}

机构：

[1] Beijing Univ Technol, Coll Mat Sci & Engn, Dept Chem Engn & Technol, Beijing Key Lab Green Catalysis & Separat,Key Lab, Beijing 100124, Peoples R China

来源：

CATALYSIS TODAY | 2024年 / 437卷

基金：

北京市自然科学基金; 中国国家自然科学基金; 中国博士后科学基金;

关键词：

Pt NPs; MOFs; Toluene oxidation; Mesoporous structure; Pt@TiO 2 catalyst; PERFORMANCE; PLASMA;

D O I：

10.1016/j.cattod.2024.114792

中图分类号：

O69 [应用化学];

学科分类号：

081704 ;

摘要：

In this work, a series of x wt% Pt@TiO2 (x = 0.18, 0.42, and 0.84) catalysts with highly dispersed Pt nanoparticles (NPs) are synthesized via pyrolysis method using Ti-based metal-organic frameworks (MOFs) as precursors. Physicochemical properties of the catalysts are characterized by a number of analytical techniques. It is shown that all samples possess mesoporous structure with surface area of 59-75.6 m2/g, thus can suppress the aggregation of Pt NPs, and enhance toluene adsorption and diffusion. The 0.84 wt% Pt@TiO2 catalyst exhibits the best catalytic performance for toluene oxidation (T90% =150 degrees C at space velocity = 20,000 mL/ (g h)), which is attributed to the higher surface area, abundant adsorbed oxygen and Pt0 species, and strong interaction between Pt NPs and TiO2. In addition, the possible reaction mechanism of toluene oxidation is proposed based on in situ DRIFTS technique.

引用

页数：10

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