Vapor-phase intramolecular aldol condensation of 2,5-hexanedione over yttrium zirconate catalyst

被引:2
|
作者
Adachi, Takuto [1 ]
Kurniawan, Enggah [1 ]
Hara, Takayoshi [1 ]
Takahashi, Ryoji [2 ]
Yamada, Yasuhiro [1 ]
Sato, Satoshi [1 ]
机构
[1] Chiba Univ, Grad Sch Engn, 1-33 Yayoi, Inage, Chiba 2638522, Japan
[2] Ehime Univ, Grad Sch Sci & Engn, 2-5 Bunkyocho, Matsuyama, Ehime 7908577, Japan
基金
日本学术振兴会;
关键词
Intramolecular aldol condensation; 5-hexanedione; Yttrium zirconate; Deactivation control; STABILIZED ZIRCONIA; BIOMASS; DEHYDRATION; BUTANEDIOLS; ETHANOL;
D O I
10.1016/j.apcata.2024.119887
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
Vapor-phase intramolecular aldol condensation of 2,5-hexanedione (2,5-HD) to 3-methyl-2-cyclopentenone (MCP) was performed over several rare-earth zirconate catalysts, with yttrium zirconate (YZrO) emerged as the most efficient catalyst. Several parameters, such as Y content, calcination temperature, reaction temperature, and contact time, highly influenced the catalytic performance of the YZrO catalyst: YZrO calcined at 700 degrees C exhibited the highest catalytic activity but still suffered from catalyst deactivation due to coke formation. Modifying the YZrO with Ag and employing the modified catalyst in an H2 flow effectively reduced the coke accumulation, thus improving the catalytic stability during the aldol condensation of 2,5-HD at 350 degrees C. The poisoning experiment with the co-fed of acidic CO2 gas and basic molecules of 2,6-, and 3,5-dimethylpyridine suggested that the aldol condensation proceeded via an acid-base concerted mechanism.
引用
收藏
页数:8
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