Platinum and Molybdenum Oxide Supported on Mesostructured Silica Nanoparticles for n-Pentane and Cyclohexane Isomerization

Fatah, N.A.A., Jalil, A.A., T. S.
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引用次数: 1

Abstract

Alkane isomerization into its equivalent branched isomers has gained numerous attention as a reaction to obtain high quality fuel. In this study, platinum and molybdenum oxide supported on mesostructured silica nanoparticles (Pt/MoO3/MSN) was prepared via impregnation method and tested for n-pentane and cyclohexane isomerization. The catalyst was characterized by using X-ray diffraction (XRD), nitrogen (N2) physisorption, and pyridine Fourier-transform infrared (pyridine-FTIR) spectroscopy. The IR result revealed that the addition of Pt and MoO3 into MSN formed different strength of Lewis and Brönsted acid sites. It was observed that the catalyst possessed strong acid sites and several numbers of relatively weak Lewis and Brönsted acid sites. Pt/MoO3/MSN was catalytically active towards n-pentane and cyclohexane isomerization with conversion of 63 and 87%, respectively, at 300 °C. It was proposed that the addition of Pt might assist the generation of active protonic acid sites from molecular hydrogen via the mechanism of hydrogen spillover and hence improve isomerization reaction.
介结构二氧化硅纳米颗粒负载的铂和钼氧化物用于正戊烷和环己烷异构化
烷烃同分异构体的异构化反应作为一种获得高质量燃料的反应受到了广泛的关注。本研究采用浸渍法制备了介结构二氧化硅纳米颗粒(Pt/MoO3/MSN)负载的铂和钼,并对其正戊烷和环己烷异构化进行了测试。采用x射线衍射(XRD)、氮(N2)物理吸附、吡啶傅里叶变换红外(pyridine- ftir)光谱对催化剂进行了表征。红外光谱结果表明,Pt和MoO3加入到MSN中形成了不同强度的Lewis和Brönsted酸位。结果表明,该催化剂具有较强的酸位和若干较弱的路易斯酸位和Brönsted酸位。Pt/MoO3/MSN在300℃下对正戊烷和环己烷异构化具有催化活性,转化率分别为63%和87%。提出Pt的加入可能通过氢溢出机制促进氢分子生成活性质子酸位点,从而改善异构化反应。
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