Photoelectrocatalytic degradation of ethylene by a combination of TiO2 and activated carbon felts

被引:57
作者
Ye, Sheng-ying [1 ]
Tian, Qing-mei [1 ]
Song, Xian-liang [1 ]
Luo, Shu-can [1 ]
机构
[1] S China Agr Univ, Coll Food Sci, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Ethylene; Photoelectrocatalytic; Titanium dioxide; Activated carbon felts; Storage; PHOTOCATALYTIC OXIDATION; REMOVAL; TOLUENE; FIBER; FRUIT; DYE;
D O I
10.1016/j.jphotochem.2009.08.001
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
Postharvest loss of quality is an important problem in the food and horticultural product industry. One of the major factors contributing to loss of quality is the uncontrolled exposure of the products to small amounts of ethylene gas during storage. In this Study we investigated the photoelectrocatalytic (PEC) degradation of ethylene gas at a temperature of 3 +/- 1 degrees C and relative humidity of 90 +/- 3% on an activated carbon felts (ACF)-supported photocatalyst titanium dioxide photoelectrode [TiO2/ACF] or on a photoelectrode which had been modified by coating the ACF Support with platinum [TiO2/ACF-Pt]. The apparent pseudo-first-order kinetic model was used to describe the PEC degradation of ethylene. The key designing parameters for a PEC reactor affecting the degradation efficiency in terms of the rate constant of this model were studied, including the bias voltage and the light intensity. Degradation of ethylene by applying a bias voltage to the [TiO2/ACF] vertical bar Nafion vertical bar [TiO2/ACF] electrode-membrane assembly or to the [TiO2/ACF-Pt] vertical bar Nafion vertical bar [TiO2/ACF-Pt] electrode-membrane assembly enhanced the efficiency of photocatalytic (PC) degradation. The combination of the ACF support modified with platinum and the applied bias voltage were found to have an additive enhancement effect on the rate constant compared to PEC degradation carried out using the unmodified ACF support. With respect to the [TiO2/ACF-Pt] vertical bar Nafion vertical bar [TiO2/ACF-Pt] electrode-membrane assembly, a kinetic model was established using response surface methodology to describe the relationship between the rate constant and the affecting parameters. Optimized parameters were found to be a light intensity of 3.1 mW cm(-2) with a bias voltage of 47.5 V. Crown Copyright (C) 2009 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 35
页数:9
相关论文
共 34 条
  • [1] Abeles F. B., 1992, ETHYLENE PLANT BIOL
  • [2] AKHURI AA, 1987, RESPONSE SURFACE DES
  • [3] Improving ultraviolet light transmission in a packed-bed photoelectrocatalytic reactor for removal of oxalic acid from wastewater
    An, Taicheng
    Xiong, Ya
    Li, Guiying
    Zhu, Xihai
    Sheng, Guoying
    Fu, Jiamo
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2006, 181 (2-3) : 158 - 165
  • [4] MECHANISTIC STUDIES OF WATER DETOXIFICATION IN ILLUMINATED TIO2 SUSPENSIONS
    BAHNEMANN, D
    BOCKELMANN, D
    GOSLICH, R
    [J]. SOLAR ENERGY MATERIALS, 1991, 24 (1-4): : 564 - 583
  • [5] Bansal R.C., 1988, ACTIVE CARBON
  • [6] Box G., 2005, Statistics for Experimenters, VSecond
  • [7] Evaluation of color removal and degradation of a reactive textile azo dye on nanoporous TiO2 thin-film electrodes
    Carneiro, PA
    Osugi, ME
    Sene, JJ
    Anderson, MA
    Zanoni, MVB
    [J]. ELECTROCHIMICA ACTA, 2004, 49 (22-23) : 3807 - 3820
  • [8] Bimodal mesoporous TiO2-P25 composite thick films with high photocatalytic activity and improved structural integrity
    Chen, Yongjun
    Dionysiou, Dionysios D.
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2008, 80 (1-2) : 147 - 155
  • [9] The photoelectrocatalytic oxidation of aqueous nitrophenol using a novel reactor
    Christensen, PA
    Egerton, TA
    Kosa, SAM
    Tinlin, JR
    Scott, K
    [J]. JOURNAL OF APPLIED ELECTROCHEMISTRY, 2005, 35 (7-8) : 683 - 692
  • [10] Preparation of Pt catalysts supported on activated carbon felts (ACF)
    de Miguel, SR
    Villella, JI
    Jablonski, EL
    Scelza, OA
    de Lecea, CSM
    Linares-Solano, A
    [J]. APPLIED CATALYSIS A-GENERAL, 2002, 232 (1-2) : 237 - 246