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Isomerization-cracking of n-octane on catalysts based on heteropolyacid H3Pw12O40 and heteropolyacid supported on zirconia and promoted with Pt and Cs

机译:正辛烷在杂多酸H3Pw12O40和负载在氧化锆上并由Pt和Cs促进的杂多酸的催化剂上的异构化裂解

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Isomerization - cracking of n-octane was studied using H3PW12O40 (HPA) and HPA supported on zirconia and promoted with Pt and Cs. The addition of Pt and Cs to the supported HPA did not modify the Keggin structure. The Pt addition to the supported HPA did not substantially modify the total acidity; however, the Brönsted acidity increased significantly. Cs increased the total acidity and Brönsted acidity. A linear relation was observed between the n-C8 total conversion and Brönsted acidity. The most adequate catalysts for performing isomerization and cracking to yield high research octane number (RON) are those with higher values of Brönsted acidity.
机译:异构化-使用H3PW12O40(HPA)和负载在氧化锆上并用Pt和Cs促进的HPA研究了正辛烷的裂解。在支持的HPA中添加Pt和Cs不会改变Keggin结构。负载的HPA中添加的Pt基本上不会改变总酸度。但是,布朗斯台德酸度显着增加。 Cs增加了总酸度和Brönsted酸度。在n-C8总转化率和布朗斯台德酸度之间观察到线性关系。进行异构化和裂化以产生高研究辛烷值(RON)的最合适的催化剂是布朗斯台德酸度较高的催化剂。

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