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- W1520444516 abstract "Hydroisomerization and hydrocracking are widely recognized as versatile reactions. They allow not only converting feeds of various origin and quality into high-value blendstocks but also identifying the opportunities brought about by different solid acids with characteristic framework structures to tailor activity and product selectivity. The bifunctional reaction mechanism is an essential feature in this respect. It comprises acid-catalyzed rearrangement and cracking in addition to metal-catalyzed (de)hydrogenation and is effective at relatively mild operating conditions. Innumerable combinations of metal and acid functions, ranging, respectively, from sulfided transition metals to noble ones and from crystalline, microporous to wider pore, amorphous materials are available for ensuring the required catalytic performance to convert the feed into the desired product slate. An adequate understanding of the detailed reaction mechanism represents a crucial element in this endeavor. Over the years an interesting evolution from simple, lumped model toward advanced ones accounting for all potentially occurring elementary steps could be discerned. Hydrocracking has been among the first reactions involved in hydrocarbon fuel production and regained popularity in the last years because of the processing of ever more heavy crudes. Its horizon, however, extends beyond the fossil era with applications in bio-fuel production and plastic waste valorization. It ensures a bright future for a historical and reliable conversion process." @default.
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- W1520444516 date "1997-07-01" @default.
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- W1520444516 title "SO42−–ZrO2and Pt/SO42−–ZrO2: Activity and Stability duringn-Hexane Isomerization" @default.
- W1520444516 doi "https://doi.org/10.1006/jcat.1997.1690" @default.
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