Mechanistic Investigations of Liquid-phase Direct Alkylation of Benzene with <i>n</i>-Heptane Using Proton-exchanged Montmorillonite Catalysts
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- TAKABATAKE Moe
- Dept. of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology
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- NAMBO Masayuki
- Dept. of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology
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- MANAKA Yuichi
- Dept. of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology Renewable Energy Research Center, National Institute of Advanced Industrial Science and Technology (AIST)
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- MOTOKURA Ken
- Dept. of Chemical Science and Engineering, School of Materials and Chemical Technology, Tokyo Institute of Technology PRESTO, Japan Science and Technology Agency (JST)
Bibliographic Information
- Other Title
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- プロトン交換モンモリロナイト触媒を用いた<i>n</i>-ヘプタンによるベンゼンの液相直接アルキル化の反応機構
- Mechanistic Investigations of Liquid-phase Direct Alkylation of Benzene with n-Heptane Using Proton-exchanged Montmorillonite Catalysts
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Abstract
<p>The direct alkylation of benzene with n-heptane was investigated using noble-metal-free montmorillonite as a solid acid catalyst. It was found that the catalytic activity of proton-exchanged montmorillonite increased after pretreatments such as heating and ultrasonic irradiation. Aluminum-exchanged montmorillonite was also found to be a good catalyst. Moreover, during the reaction using proton-exchanged montmorillonite, the product selectivity depended on the interlayer distance of the catalyst. Detailed time-course analysis of the selectivity of the alkylation product revealed that, in the case of the catalysts with smaller interlayer distances, the bimolecular reaction occurred preferentially at the surface, resulting in higher selectivity with respect to the target C7 alkylated products (Ph-C7). On the other hand, the monomolecular cracking of heptane in the interlayer spaces resulted in a stable t-butyl cation, yielding t-butylbenzene. Monomolecular cracking also occurred when H-ZSM-5 was used as the catalyst, and the main product was isopropylbenzene.</p>
Journal
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- Journal of the Japan Petroleum Institute
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Journal of the Japan Petroleum Institute 63 (5), 289-296, 2020-09-01
The Japan Petroleum Institute
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Details 詳細情報について
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- CRID
- 1390566775163778816
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- NII Article ID
- 130007895038
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- NII Book ID
- AA11590615
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- ISSN
- 1349273X
- 13468804
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- NDL BIB ID
- 030648468
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed