Compensation between activation entropy and enthalpy in reactions of aromatic hydrocarbons catalyzed by solid acids

被引:16
作者
Nakamura, Koshiro [1 ]
Mizuta, Ryo [1 ]
Suganuma, Satoshi [2 ]
Tsuji, Etsushi [1 ]
Katada, Naonobu [1 ]
机构
[1] Tottori Univ, Dept Chem & Biotechnol, Grad Sch Engn, Minami Ku, 4-101 Koyama Cho, Tottori 6808552, Japan
[2] Tottori Univ, Ctr Res Green Sustainable Chem, Fac Engn, Minami Ku, 4-101 Koyama Cho, Tottori 6808552, Japan
关键词
Activation entropy; Activation enthalpy; Zeolite; Silica-alumina; Toluene disproportionation; Cumene cracking; TEMPERATURE-PROGRAMMED DESORPTION; CRACKING; ZEOLITES; AMMONIA; ALKANES; SITES; DISPROPORTIONATION; TRANSALKYLATION; THERMODYNAMICS; ALKYLBENZENES;
D O I
10.1016/j.catcom.2017.08.033
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
Reaction rates of toluene disproportionation (A) and cumene cracking (B) normalized by the number of Bronsted acid sites were analyzed on aluminosilicates. The activation entropy showed linear and compensatory relationship against the activation enthalpy. The slope of entropy-enthalpy plot was in the order of (B) > (A) > small alkane cracking, whereas the intercept on the horizontal axis was in the order of propane and isobutane cracking > linear C4-8 alkanes and iso-pentane cracking > (A) > (B). The former is consistent with the bulkiness of reactant, while the latter is consistent with intrinsic difficulty of formation of intermediate cations.
引用
收藏
页码:103 / 107
页数:5
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