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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
来源:
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.
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页码:4621 / 4627
页数:7
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