Conversion of 1-and 2-Tetralone Over HY Zeolite

被引:3
作者
Prasomsri, Teerawit [1 ,4 ]
Tailleur, Roberto E. Galiasso [1 ,4 ]
Alvarez, Walter E. [2 ]
Sooknoi, Tawan [3 ]
Resasco, Daniel E. [1 ,4 ]
机构
[1] Univ Oklahoma, Ctr Biomass Refining, Norman, OK 73019 USA
[2] ConocoPhillips Res Ctr, Bartlesville, OK 74004 USA
[3] King Mongkuts Inst Technol, Dept Chem, Fac Sci, Bangkok 10520, Thailand
[4] Univ Oklahoma, Sch Chem Biol & Mat Engn, Norman, OK 73019 USA
基金
美国国家科学基金会;
关键词
Oxygenated aromatic; 1-Tetralone; 2-Tetralone; Tetralin; Dihydronaphthalene; Naphthalene; Tetralol; Naphthol; Thermal reaction; HY; Zeolite; HYDROGEN-TRANSFER; TETRALIN; CRACKING; DECALIN; MOLECULES;
D O I
10.1007/s10562-010-0308-1
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
Conversion of 1- and 2-tetralone was investigated over acid HY zeolite under various reaction conditions in the vapor phase. Reactions were conducted in a fixed-bed reactor at 300, 400 and 500 degrees C in hydrogen atmospheric pressure. It was found that 1- and 2-tetralone are thermally unstable and thermal reaction has a contribution, particularly at high temperatures. The reactivity of 2-tetralone was significantly higher than that of 1- tetralone. This behavior is more pronounced in the presence of acid HY zeolite. For both isomers, the main products were naphthol, coupling compounds (4-ring), naphthalene and tetralin. Trace amounts of dihydronaphthalene, ring-contraction and ring-opening product were also observed. At high temperatures, isomerization and dehydration of naphthol were observed over the HY zeolite. It seems that on the acidic zeolite, hydrogen transfer plays a significant role in determining the reaction path.
引用
收藏
页码:226 / 232
页数:7
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