Shape-selective diisopropylation of naphthalene in H-Mordenite: Myth or reality?

Journal of Catalysis

Volumn 270, Issue 1, 2010, Pages 60-66

  Bouvier, Christophe ^a   Buijs, Wim ^a   Gascon, Jorge ^a   Kapteijn, Freek ^a   Gagea, Bogdan C ^b   Jacobs, Pierre A ^b   Martens, Johan A ^b  

^a DELFT UNIVERSITY OF TECHNOLOGY   (Netherlands)

^b UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

2,6 Diisopropylnaphthalene; H MOR; H USY; Kinetic mixture; Molecular modeling; Shape selectivity; Thermodynamical distribution

Indexed keywords

2,6-DIISOPROPYLNAPHTHALENE; ACTIVE CATALYST; COMPUTATIONAL WORK; H-MOR; H-MORDENITE; HIGH REACTION TEMPERATURES; POSITIONAL ISOMERS; SHAPE SELECTIVITY; THERMODYNAMIC EQUILIBRIA; ULTRASTABLE Y;

CATALYSIS; ISOMERS; MIXTURES; MOLECULAR MODELING; NAPHTHALENE; SILICATE MINERALS; ZEOLITES;

CATALYST SELECTIVITY;

EID: 76749135656     PISSN: 00219517     EISSN: 10902694     Source Type: Journal    
DOI: 10.1016/j.jcat.2009.12.005     Document Type: Article

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