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n-Heptane hydroconversion over sulfated-zirconia-supported molybdenum carbide catalysts

机译:硫酸盐氧化锆负载碳化钼催化剂上的正庚烷加氢转化

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Molybdenum carbide on sulfated zirconia was prepared by impregnation of MoO3 on sulfated zirconia to give a loading of 5?wt% followed by carburisation at 923?K in a mixture of CH4/H2 (4:1). The resulting catalyst was characterised by N2 adsorption–desorption, CO chemisorption, FTIR of pyridine adsorption, XRD, TPR, TGA, Raman and SEM–EDX. This combination of characterisation studies suggests formation of a well-dispersed Mo2C phase over tetragonal zirconia. When employed in the hydroconversion of n-heptane, high temperature and low space velocity lead to substantial cracking. However, under some conditions, an increase in the research octane number (RON) from 0 (n-heptane) to ca. 50 was attained. Between 723 and 873?K, n-heptane is mainly cracked to iso-pentane and ethane. The product distribution as a function of conversion suggests that the reaction did not simply follow a consecutive reaction pathway, but that other parallel routes were involved.
机译:硫酸钼氧化锆上的碳化钼是通过将MoO3浸渍在硫酸氧化锆上制成5重量%的负载量,然后在923?K的CH4 / H2(4:1)混合物中渗碳。所得催化剂的特征在于氮气吸附-解吸,CO化学吸附,吡啶吸附的FTIR,XRD,TPR,TGA,拉曼和SEM-EDX。表征研究的这种组合表明在四方氧化锆上形成了分散良好的Mo2C相。当用于正庚烷的加氢转化中时,高温和低空速导致大量裂化。但是,在某些情况下,研究辛烷值(RON)从0(正庚烷)增加到大约1。达到50。在723至873?K之间,正庚烷主要裂化为异戊烷和乙烷。产物分布作为转化的函数表明该反应不仅仅遵循连续的反应路径,而且还涉及其他平行路径。

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