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Selective ring opening of naphthenic molecules

机译:环烷烃分子的选择性开环

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Increasingly stringent environmental regulations require significant quality improvements in both gasoline and diesel fuels. Specifications for diesel will likely include ultra low sulfur and reduced multiring aromatic contents. Such mandates can be met by a combination of deep hydrodesulfurization and aromatic saturation. Further diesel quality improvements are possible by lowering density and increasing cetane value by selective ring opening (SRO) single and multiring naphthenes present in mid-distillate streams into acyclic paraffins. Noble metal based hydrogenolysis catalysts such as platinum and iridium are quite effective for selectively ring opening five-membered ring naphthenes such as methylcyclopentane. Ring opening of six-membered-ring are, in contrast, much more difficult to open via a hydrogenolysis route [1]. Strongly acidic hydrocracking catalysts readily covert naphthenic molecules but the primary ring opened products undergo rapid secondary reactions to lighter molecules [2,3,4]. To achieve significant diesel quality improvements it will be necessary to selectively convert alkyl substituted molecules in mid-distillate feedstocks.
机译:日益严格的环境法规要求汽油和柴油燃料的质量都有显着提高。柴油的规格可能包括超低硫和降低的多环芳烃含量。深度加氢脱硫和芳烃饱和的组合可以满足这些要求。通过降低存在于中间馏分流中的无环烷烃的选择性开环(SRO)单环和多环环烷烃,降低密度并提高十六烷值,可以进一步改善柴油质量。基于贵金属的氢解催化剂如铂和铱对于选择性开环五元环烷烃如甲基环戊烷是非常有效的。相比之下,六元环的开环更难通过氢解途径打开[1]。强酸性加氢裂化催化剂很容易使环烷烃分子隐蔽,但开环的初级产物会迅速发生次级反应,生成较轻的分子[2,3,4]。为了实现柴油质量的显着提高,有必要在馏分中间原料中选择性地转化烷基取代的分子。

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