Efficient Conversion of Bio-Lactic Acid to 2,3-Pentanedione on Cesium-Doped Hydroxyapatite Catalysts with Balanced Acid-Base Sites

被引:31
|
作者
Li, Xinli [1 ]
Sun, Liangwei [2 ]
Zou, Weixin [3 ]
Cao, Ping [1 ]
Chen, Zhi [1 ]
Tang, Congming [1 ,2 ]
Dong, Lin [3 ]
机构
[1] Chongqing Univ Technol, Sch Chem & Chem Engn, Chongqing 40054, Peoples R China
[2] China West Normal Univ, Chem Synth & Pollut Control Key Lab Sichuan Prov, Nanchong 637002, Sichuan, Peoples R China
[3] Nanjing Univ, Jiangsu Key Lab Vehicle Emiss Control Ctr Modern, Nanjing 210093, Jiangsu, Peoples R China
关键词
biomass; calcium; C-C coupling; cesium; ketones; ACRYLIC-ACID; HIGHLY EFFICIENT; PHOSPHATE CATALYSTS; DEHYDRATION; GLYCEROL; ACETALDEHYDE; PERFORMANCE; DECARBONYLATION; OXIDATION; ETHANOL;
D O I
10.1002/cctc.201701332
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
We report the design and synthesis of cesium-doped hydroxyapatite for direct and high-yield conversion of biobased lactic acid to 2,3-pentanedione (72.3%). Cs species derived from CsNO3 at high temperature of calcination is introduced into the hydroxyapatite structure to regulate its acid-base properties. It is found that a balance of acid-base chemistry favors the condensation of lactic acid to 2,3-pentanedione. As a result, the undesired reactions such as lactic acid dehydration, decarbonylation, and coking are suppressed. Instead, a concerted catalysis between surface basic site and acidic site for lactic acid condensation to 2,3-pentanedione dominates on the cesium-doped hydroxyapatite catalyst, leading to a highly selective process for direct conversion of bio-lactic acid to 2,3-pentanedione.
引用
收藏
页码:4621 / 4627
页数:7
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