Nucleophilic Reactions of Bromocyclopentane in the Structure-H Methane plus Bromocyclopentane Mixed Hydrate System at High Pressures

被引:4
|
作者
Matsumoto, Yuuki [1 ]
Katsuta, Yoshito [1 ]
Kamo, Fumitaka [1 ]
Bando, Tatsuya [1 ]
Makino, Takashi [2 ]
Sugahara, Takeshi [1 ]
Ohgaki, Kazunari [1 ]
机构
[1] Osaka Univ, Grad Sch Engn Sci, Div Chem Engn, Dept Mat Engn Sci, Toyonaka, Osaka 5608531, Japan
[2] Natl Inst Adv Ind Sci & Technol, Sendai, Miyagi 9838551, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2014年 / 118卷 / 47期
关键词
MOLECULE GUEST SUBSTANCES; PHASE-EQUILIBRIUM; THERMODYNAMIC STABILITY; CLATHRATE HYDRATE; WATER-SYSTEMS; GAS HYDRATE; 15; KBAR; CYCLOPENTANE; BOUNDARIES; TETRAHYDROPYRAN;
D O I
10.1021/jp505313v
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Thermodynamic stability boundary in the structure-H methane + bromocyclopentane mixed hydrate system was measured at pressures from 20 to 100 MPa. The thermodynamic stability boundary of the methane + bromocyclopentane mixed hydrate exhibits anomalous behavior under conditions at high pressures and high temperatures. This phenomenon is due to the elimination and substitution reactions of bromocyclopentane to cyclopentene and cyclopentanol, respectively. The nucleophilic reactions of bromocyclopentane are mainly advanced in the liquid bromocyclopentane-rich phases, while it is restrained when bromocyclopentane is enclathrated in hydrate cage.
引用
收藏
页码:13404 / 13408
页数:5
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