Liquid phase catalytic hydrodechlorination of 2,4-dichlorophenol over Pd/Al2O3: Batch vs. continuous operation

被引:46
作者
Gomez-Quero, Santiago [1 ]
Cardenas-Lizana, Fernando [1 ]
Keane, Mark A. [1 ]
机构
[1] Heriot Watt Univ, Sch Engn & Phys Sci, Edinburgh EH14 4AS, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
Catalytic hydrodechlorination; 2,4-Dichlorophenol; Pd/Al2O3; catalyst; Batch reactor; Continuous reactor; SUPPORTED PALLADIUM CATALYSTS; SUPERCRITICAL CARBON-DIOXIDE; WASTE-WATER TREATMENT; NICKEL-CATALYSTS; BIMETALLIC MIXTURE; RH CATALYSTS; NI-AU; CHLOROPHENOLS; PD; PENTACHLOROPHENOL;
D O I
10.1016/j.cej.2010.07.032
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The three-phase (atmospheric pressure, T=303 K, bulk solution pH 12) catalytic hydrodechlorination (HDC) of 2,4-dichlorophenol (2,4-DCP) over Pd/Al2O3 has been studied in batch and continuous flow reactors. In both cases, 2,4-DCP yielded 2-chlorophenol and phenol as products of partial and complete HOC, respectively. Cyclohexanone, resulting from further ring hydrogenation, was also isolated but was formed with low selectivity (<= 4%). Conditions have been established in both reactors where HOC proceeds under catalytic control. A move from discontinuous to continuous operation resulted in a more efficient (five-fold) H-2 transfer, which can be attributed to an extended gas/liquid interface available for mass transport. Higher HDC rate and increased selectivity to phenol were obtained in the continuous flow reactor, which we attribute to a lower pH at the liquid/solid interface relative to batch operation. Furthermore, the productive catalyst lifetime was extended in the flow reactor due to the more effective removal of HCl from the catalyst surface. The results presented establish the feasibility of continuous, liquid phase HOC under mild conditions as a means of treating environmentally toxic 2,4-DCP. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1044 / 1051
页数:8
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