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Hydrocarbon-pool chemistry is important in methanol to olefins (MTO) conversion on acidic zeolite catalysts. The hydrocarbon-pool (HP) species, such as methylbenzenes and cyclic carbocations, confined in zeolite channels during the reaction are essential in determining the reaction pathway. Herein, we experimentally demonstrate the formation of supramolecular reaction centers composed of organic hydrocarbon species and the inorganic zeolite framework in H-ZSM-5 zeolite by advanced 13C-27Al double-resonance solid-state NMR spectroscopy. Methylbenzenes and cyclic carbocations located near Brønsted acid/base sites form the supramolecular reaction centers in the zeolite channel. The internuclear spatial interaction/proximity between the 13C nuclei (associated with HP species) and the 27Al nuclei (associated with Brønsted acid/base sites) determines the reactivity of the HP species. The closer the HP species are to the zeolite framework Al, the higher their reactivity in the MTO reaction. [ABSTRACT FROM AUTHOR]

The methanol to olefins conversion over zeolite catalysts is a commercialized process to produce light olefins like ethene and propene but its mechanism is not well understood. We herein investigated the formation of ethene in the methanol to olefins reaction over the H-ZSM-5 zeolite. Three types of ethylcyclopentenyl carbocations, that is, the 1-methyl-3-ethylcyclopentenyl, the 1,4-dimethyl-3-ethylcyclopentenyl, and the 1,5-dimethyl-3-ethylcyclopentenyl cation were unambiguously identified under working conditions by both solid-state and liquid-state NMR spectroscopy as well as GC-MS analysis. These carbocations were found to be well correlated to ethene and lower methylbenzenes (xylene and trimethylbenzene). An aromatics-based paring route provides rationale for the transformation of lower methylbenzenes to ethene through ethylcyclopentenyl cations as the key hydrocarbon-pool intermediates. [ABSTRACT FROM AUTHOR]

A secondary amino-modified mesoporous molecular sieve MCM-41 was obtained by reaction of bis(3-(triethoxysilyl)propyl)amine with MCM-41. The chiral Salen-Mn (III) complex was anchored onto the modified MCM-41 by a multi-step grafting method and two heterogenized catalysts with different Mn contents were obtained. The catalysts were characterized by XRD, N2 adsorption, ICP, FT-IR and DR UV-Vis. Their catalysis on asymmetric epoxidation of several olefins was studied with NaCIO and m-CPBA as oxidants respectively. It was found that both the activity and enantioselectivity of the catalysts decreased after the homogeneous catalyst was heterogenized. The reasons resulting in the decrease of catalytic performance were discussed. [ABSTRACT FROM AUTHOR]

The hydrocarbon pool (HP) species in methanol-to-olefins (MTO) reactions over zeolite H-ZSM-5 were investigated by solid-state NMR spectroscopy and GC–MS. The distribution and reactivity of retained HP species such as carbocations and methylbenzenes (MBs) were found to evolve with reaction time and their positions in the catalyst bed. The underlying mechanism of the typical S-shaped methanol conversion curve was revealed, in which the dominating reaction route was found to be dependent on the formation and reactivity of different HP species that were varied at different reaction time. During the induction period, cyclopentenyl cations served as the precursor to MBs and exhibited higher reactivity than the latter. The reaction was accelerated by the accumulation of alkenes and further enhanced by consequent involvement of the cyclopentenyl cations and aromatics, which eventually led to a steady state reaction. The interconversions of the reaction cycles based on alkenes, cyclopentenyl cations, and MBs were proposed for the formation of light olefins. The co-catalysis of HP species in the MTO reactions showed that the cyclopentenyl cations and alkenes favored propene formation, while the light MBs such as xylene and triMB facilitated ethene formation. Within the catalyst bed, both cyclopentenyl cations and MBs were dominantly formed in the upper catalyst layers. The experiments indicated that both cyclopentenyl cations and alkenes maintained high reactivity throughout the catalytic bed, while MBs exhibited high reactivity only in the upper catalyst position. [ABSTRACT FROM AUTHOR]

The formation and reactivity of a methylbenzenes (MBs) hydrocarbon pool in the induction period of the methanol-to-olefins (MTO) reaction over zeolite H-ZSM-5 was investigated and the mechanistic link of MBs to ethene and propene was revealed. Time evolution analysis of the formed MBs and 12 C/ 13 C methanol-switching experiments indicate that in the induction period bulkier compounds such as tetraMB and pentaMB have higher reactivity than their lighter counterparts such as p/m-diMB and triMB. By correlating the distribution of MBs trapped on H-ZSM-5 with ethene and propene, we found that tetraMB and pentaMB favor the formation of propene, while p/m-diMB and triMB mainly contribute to the formation of ethene. On the basis of this relationship, the olefin (ethene and propene) selectivity can be controlled by regulating the distribution of trapped MBs by varying the silicon-to-aluminum ratio of ZSM-5, reaction temperature, and space velocity. The reactivity of MBs and the correlation of MBs with olefins were also verified under steady-state conditions. By observation of key cyclopentenyl and pentamethylbenzenium cation intermediates using in situ solid-state NMR spectroscopy, a paring mechanism was proposed to link MBs with ethene and propene. P/M-diMB and triMB produce ethylcyclopentenyl cations followed by splitting off of ethene, while tetraMB and pentaMB generate propyl-attached intermediates, which eventually produce propene. This work provides new insight into the MBs hydrocarbon pool in MTO chemistry. [ABSTRACT FROM AUTHOR]