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Simultaneous isomerization of n-heptane and hydrogenation of benzene over bimetallic PtMe/Beta catalysts in the absence and presence of sulfur

机译:在硫磺和存在的情况下,对二氧化硅PTME /β催化剂的N-庚烷和苯氢化的同时异构化

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Bifunctional bimetallic PtMe/Beta catalysts (Me = Pd, Ir, Ru) have been prepared and studied for the simultaneous isomerization of n-heptane and hydrogenation of benzene. In the absence of sulfur, PtPd samples were less selective to iso-C_7 than PtIr and PtRu. The extent of cracking increased with the Pd concentration in PtPd/Beta. The conversion of benzene was 100% for all catalysts. In the presence of 200 ppm sulfur, the n-C_7 conversion decreased while the cracking selectivity increased. The relative decrease of activity was lower for PtPd catalysts, suggesting a higher sulfur resistance as compared to PtIr and PtRu. Benzene conversion was much less affected by sulfur, but there was a loss of activity for isomerization of cyclohexane into methylcyclopentane. The better sulfur resistance of PtPd samples may arise from a stabilization of partially charged Pt~(δ+) species by interaction with Pd, which could be associated with a lower reducibility of Pt~(2+) in presence of Pd, as observed by TPR.
机译:双功能双金属PTME /β催化剂(ME =钯,铱,钌)已经制备并研究了正庚烷和苯的氢化的同时异构化。在不存在的硫,的PtPd样品到异C_7比PTIR和的PtRu选择性较低。的程度与在的PtPd /βPd浓度裂纹增加。苯的转化是所有催化剂100%。在200ppm的硫的存在,该n C_7转换而开裂选择性的增加而降低。活性的相对减少,降低了的PtPd催化剂,相比于PTIR和的PtRu提示有较高的硫电阻。苯的转化率要少得多硫影响,但有环己烷异构化为甲基环戊烷活性的丧失。的PtPd样品的更好硫电阻可以从部分充电的Pt〜的稳定化引起(δ+)物种通过用Pd相互作用,这可能有Pt〜(2+)的在Pd存在下的较低还原性相关,通过所观察到的TPR。

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