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Study of Mn-based catalysts for oxidative dehydrogenation of cyclohexane to cyclohexene

机译:study of mn-based catalysts for oxidative dehydrogenation of cyclohexane to cyclohexene

摘要

The gas-phase oxidative dehydrogenation (ODH) of cyclohexane to cyclohexene in the presence of molecular oxygen has been studied over various Mn-based catalysts. It is found that LiCl/MnOx/PC (Portland cement) catalyst exhibits the highest catalytic performance, and a 42.8% cyclohexane conversion, 58.8% cyclohexene selectivity and 25.2% cyclohexene yield can be achieved under 600 degrees C, 20,000 h(-1) and C6H12/O-2/N-2= 14/7/79. There are good correlations between the selectivities to cyclohexene and the electrical conductivities of Li doped Mn-based catalysts, from which it is deduced that the non-fully reduced oxygen species (O-2(-), O-2(2-), O-) involved in a new phase of LiMn2O4 might be responsible for the high selectivity toward cyclohexene, whereas the Mn2O3 crystal phase results in the COx formation. The selectivity to cyclohexene increases with increasing molar ratio of Li to Mn in LiCl/ MnOx/PC.
机译:已经在各种锰基催化剂上研究了在分子氧存在下环己烷的气相氧化脱氢(ODH)生成环己烯。发现LiCl / MnOx / PC(波特兰水泥)催化剂表现出最高的催化性能,在600摄氏度,20,000 h(-1)下可以达到42.8%的环己烷转化率,58.8%的环己烯选择性和25.2%的环己烯收率。 C6H12 / O-2 / N-2 = 14/7/79。对环己烯的选择性与掺杂锂的Mn基催化剂的电导率之间存在良好的相关性,由此可以推断出未完全还原的氧种类(O-2(-),O-2(2-), LiMn2O4的新相中所涉及的O-)可能是对环己烯的高选择性的原因,而Mn2O3晶相会导致COx的形成。在LiCl / MnOx / PC中,随着Li与Mn摩尔比的增加,对环己烯的选择性增加。

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