Degradation of high concentration 2,4-dichlorophenol by simultaneous photocatalytic-enzymatic process using TiO2/UV and laccase

Degradation of high concentration 2,4-dichlorophenol by simultaneous photocatalytic-enzymatic process using TiO2/UV and laccase
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使用 TiO2/UV 和漆酶同步光催化酶法降解高浓度 2,4-二氯苯酚

DOI:
10.1016/j.jhazmat.2011.12.052
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发表时间:
2012-02-29
影响因子:
13.6
通讯作者:
Wang, Huajun
Wang, Huajun
中科院分区:
环境科学与生态学1区
文献类型:
--
作者:
Jia, Jingbo;Zhang, Songping;Wang, Huajun

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Removal of 2,4-dichlorophenol (2,4-DCP) by TiO2/UV photocatalytic, laccase, and simultaneous photocatalytic-enzymatic treatments were investigated. Coupling of native laccase with TiO2/UV showed a negative synergetic effect due to the rapid inactivation of laccase. Immobilizing laccase covalently to controlled porous glass (CPG) effectively enhanced the stability of laccase against TiO2/UV induced inactivation. By coupling CPG-laccase with the TiO2/UV the degradation efficiency of 2,4-DCP was significantly increased as compared with the results obtained when immobilized laccase or TiO2/UV were separately used. Moreover, the enhancement was more remarkable for the degradation of 2,4-DCP with high concentration, such that for the degradation of 5 mM 2,4-DCP, 90% removal percentage was achieved within 2 h with the coupled degradation process. While for the TiO2/UV and CPG-laccase process, the removal percentage of 2,4-DCP at 2 h were only 26.5% and 78.1%, respectively. The degradation kinetics were analyzed using a intermediate model by taking into account of the intermediates formed during the degradation of 2,4-DCP. The high efficiency of the coupled degradation process therefore provided a novel strategy for degradation of concentrated 2,4-DCP. Furthermore, a thermometric biosensor using the immobilized laccase as biorecognition element was constructed for monitoring the degradation of 2,4-DCP, the result indicated that the biosensor was precise and sensitive. (C) 2011 Elsevier B.V. All rights reserved.