Generation of diamondoid hydrocarbons as confined compounds in SAPO-34 catalyst in the conversion of methanol.

Formation of adamantane hydrocarbons and their confinement in SAPO-34 caused the long induction period and the quick catalyst deactivation in methanol conversion. Via ship-in-a-bottle synthesis, adamantane and methyladamantanes could be produced from methanol conversion in the cage of 8-ring SAPO catalysts under very mild reaction conditions.

[1]  Chun Yang,et al.  GC/MS Quantitation of Diamondoid Compounds in Crude Oils and Petroleum Products , 2006 .

[2]  K. Peters,et al.  Diamondoid hydrocarbons as indicators of natural oil cracking , 1999, Nature.

[3]  Ronghui Wang,et al.  CHARACTERISTICS AND PERFORMANCE OF SAPO-34 CATALYST FOR METHANOL-TO-OLEFIN CONVERSION , 1990 .

[4]  Michael Stöcker,et al.  Methanol-to-hydrocarbons: catalytic materials and their behavior 1 Dedicated to my wife Wencke Ophau , 1999 .

[5]  Bert M. Weckhuysen,et al.  Product shape selectivity dominates the Methanol-to-Olefins (MTO) reaction over H-SAPO-34 catalysts , 2009 .

[6]  J. F. Haw,et al.  The Prediction of Persistent Carbenium Ions in Zeolites , 1998 .

[7]  Ivar M. Dahl,et al.  On the reaction mechanism for propene formation in the MTO reaction over SAPO-34 , 1993 .

[8]  B. Arstad,et al.  The reactivity of molecules trapped within the SAPO-34 cavities in the methanol-to-hydrocarbons reaction. , 2001, Journal of the American Chemical Society.

[9]  G. Olah,et al.  Chemistry in superacids. 7. Superacid-catalyzed isomerization of endo- to exo-trimethylenenorbornane (tetrahydrodicyclopentadiene) and to adamantane , 1986 .

[10]  U. Olsbye,et al.  Coke precursor formation and zeolite deactivation: mechanistic insights from hexamethylbenzene conversion , 2003 .

[11]  Zhongmin Liu,et al.  Ultra-short contact time conversion of chloromethane to olefins over pre-coked SAPO-34: direct insight into the primary conversion with coke deposition. , 2009, Chemical communications.

[12]  B. Arstad,et al.  Methanol-to-hydrocarbons reaction over SAPO-34. Molecules confined in the catalyst cavities at short time on stream , 2001 .

[13]  Zhongmin Liu,et al.  Highly efficient catalytic conversion of chloromethane to light olefins over HSAPO-34 as studied by catalytic testing and in situ FTIR , 2006 .

[14]  Weiguo Song,et al.  Methylbenzenes Are the Organic Reaction Centers for Methanol-to-Olefin Catalysis on HSAPO-34 , 2000 .

[15]  Silvia Bordiga,et al.  The Effect of Acid Strength on the Conversion of Methanol to Olefins Over Acidic Microporous Catalysts with the CHA Topology , 2009 .

[16]  M. Guisnet,et al.  "Coke" molecules trapped in the micropores of zeolites as active species in hydrocarbon transformations , 2002 .

[17]  L. Landau,et al.  Multivariate statistical analysis of diamondoid and biomarker data from Brazilian basin oil samples , 2008 .

[18]  G. Marin,et al.  Understanding the failure of direct C-C coupling in the zeolite-catalyzed methanol-to-olefin process. , 2006, Angewandte Chemie.

[19]  Fernando Ramôa Ribeiro,et al.  Prevention of zeolite deactivation by coking , 2009 .

[20]  P. Schleyer A SIMPLE PREPARATION OF ADAMANTANE , 1957 .

[21]  K. Lillerud,et al.  Spectroscopic evidence for a persistent benzenium cation in zeolite H-beta. , 2003, Journal of the American Chemical Society.

[22]  Weiguo Song,et al.  The mechanism of methanol to hydrocarbon catalysis. , 2003, Accounts of chemical research.

[23]  J. F. Haw,et al.  Well-defined (supra)molecular structures in zeolite methanol-to-olefin catalysis , 2005 .

[24]  D. McCann,et al.  A complete catalytic cycle for supramolecular methanol-to-olefins conversion by linking theory with experiment. , 2008, Angewandte Chemie.