甲醛光催化降解与过氧化氢生成的相关性研究

华兆哲, 陈坚, 白石文秀, 中迫亚昇, 王歆鹏. 甲醛光催化降解与过氧化氢生成的相关性研究[J]. 环境化学, 2005, 24(5): 520-524.
引用本文: 华兆哲, 陈坚, 白石文秀, 中迫亚昇, 王歆鹏. 甲醛光催化降解与过氧化氢生成的相关性研究[J]. 环境化学, 2005, 24(5): 520-524.
HUA Zhao-zhe, CHEN Jian, SHIRAISHI Fumihide, NAKASAKO Tsugunori, WANG Xin-peng. RELATIONSHIP BETWEEN PHOTOCATALYTIC DEGRADATION OF FORMALDEHYDE AND FORMATION OF HYDROGEN PEROXIDE[J]. Environmental Chemistry, 2005, 24(5): 520-524.
Citation: HUA Zhao-zhe, CHEN Jian, SHIRAISHI Fumihide, NAKASAKO Tsugunori, WANG Xin-peng. RELATIONSHIP BETWEEN PHOTOCATALYTIC DEGRADATION OF FORMALDEHYDE AND FORMATION OF HYDROGEN PEROXIDE[J]. Environmental Chemistry, 2005, 24(5): 520-524.

甲醛光催化降解与过氧化氢生成的相关性研究

  • 基金项目:

    江苏省创新人才(学术)项目(No.BK2004401)

RELATIONSHIP BETWEEN PHOTOCATALYTIC DEGRADATION OF FORMALDEHYDE AND FORMATION OF HYDROGEN PEROXIDE

  • Fund Project:
  • 摘要: 分别采用两种光催化剂(TiO2与Pd/TiO2)和三种紫外光源(黑光灯、杀菌灯、臭氧灯)分解水溶液中的甲醛,同时以酶法测定光催化降解过程中生成的低浓度过氧化氢.发现波长较短的紫外光源生成过氧化氢的浓度较高.当以臭氧灯为光源时,无论是否有催化剂存在,生成的过氧化氢浓度都在50mmol·m-3以上,因为185nm以下的紫外光可以直接由水与溶解氧生成臭氧,而后生成过氧化氢.不管有无催化剂存在,在臭氧灯作用下,甲醛溶液中生成的过氧化氢浓度高于纯水中生成的过氧化氢浓度.但是,在以黑光灯或臭氧灯为光源时,上述结果正好相反.此外,对于每种光源而言,当采用Pd/TiO2代替TiO2时,甲醛的分解和过氧化氢的生成都得到加强.甲醛光催化分解速率与相同条件下纯水中过氧化氢的生成速率呈正比,表明光催化降解的活性与光催化生成过氧化氢的能力近似呈正相关.
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  • [1] Wang S, Shiraishi F, Nakano K,A Synergistic Effect of Photocatalysis and Ozonation on Decomposition of Formic Acid in an Aqueous Solution [J] .Chem. Eng.J.,2002,87:261-271
    [2] Arslan I, Balcioglu A, Bahnemann D W,Advanced Chemical Oxidation of Reactive Dyes in Simulated Dyehouse Effluents by Ferrioxalate-fenton/UV-A and TiO2/UV-A Process [J] .Dyes and Pigments,2000,47:207-218
    [3] Fallmann H, Krutzler T, Bauer R, Malato S et al.,Applicability of the Photo-Fenton Method for Treating Water Containing Pesticides [J] .J. Catalysis Today,1999,54:309-319
    [4] Hugul M, Apak R,Demirci C,Modeling the Kinetics of UV/Hydrogen Peroxide Oxidation of Some Mono-,Di-, and Trichlorophenols [J] .J.Hazard. Mat.,2000,77:193-208
    [5] Lunar L, Sicilia D, Rubio S et al.,Degradation of Photographic Developers by Fenton Reagent: Condition Optimization and Kinetics for Metol Oxidation [J] .Water Res.,2000,34:1791-1802
    [6] Nedoloujko A, Kiwi J,TiO2 Speciation Precluding Mineralization of 4-Tert-butylpyridine Accelerated Mineralization via Fenton photo-assisted reaction [J] .Water Res.,2000,34:3277-3284
    [7] Matsuo K, Takeshita T, Nakano K,Formation of Thin Films by the Treatment of Amorphous Tatiana with H2O2[J] . J. Crystal Growth,1990,99:621-624.
    [8] Xu J-H, Shiraishi F,Photocatalytic Decomposition of Acetaldehyde in Air Over Titanium Dioxide [J] .J.Chem.Technol. Biotechnol.,1999,74:1096-1100
    [9] Wang S, Shiraishi F,Decompositions of Formic Acid in Two Types of Photocatalytic Reactors--Effects of Film-Diffusional Resistance and Penetration of UV Light on Decomposition Rates [J] .Eco-Engineering,2002,14:9
    [10] Fukinbara S, Shiraishi F, Nakano K,Characteristics of the Photocatalytic Reactor with an Annular Array of Glass Tubes Surrounding a Light Source: 1.Selection of a Light Source and Photocatalyst Support [J] .CELSS J.,2001,13:1-10
    [11] Fukinbara S, Shiraishi F,Characteristics of the Photocatalytic Reactor with an Annular Array of Glass Tubes Surrounding a Light Source: 2.Kinetic Analysis [J] .CELSS J.2001,13:11-13
    [12] Beltran F J, Garcia-Araya J F, Acedo B,Advanced Oxidation of Atrazine in Water. II. Ozonization Combined with Ultraviolet Radiation [J] .Water Res.,1994,28:2165-2174.
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  • 收稿日期:  2004-12-24
华兆哲, 陈坚, 白石文秀, 中迫亚昇, 王歆鹏. 甲醛光催化降解与过氧化氢生成的相关性研究[J]. 环境化学, 2005, 24(5): 520-524.
引用本文: 华兆哲, 陈坚, 白石文秀, 中迫亚昇, 王歆鹏. 甲醛光催化降解与过氧化氢生成的相关性研究[J]. 环境化学, 2005, 24(5): 520-524.
HUA Zhao-zhe, CHEN Jian, SHIRAISHI Fumihide, NAKASAKO Tsugunori, WANG Xin-peng. RELATIONSHIP BETWEEN PHOTOCATALYTIC DEGRADATION OF FORMALDEHYDE AND FORMATION OF HYDROGEN PEROXIDE[J]. Environmental Chemistry, 2005, 24(5): 520-524.
Citation: HUA Zhao-zhe, CHEN Jian, SHIRAISHI Fumihide, NAKASAKO Tsugunori, WANG Xin-peng. RELATIONSHIP BETWEEN PHOTOCATALYTIC DEGRADATION OF FORMALDEHYDE AND FORMATION OF HYDROGEN PEROXIDE[J]. Environmental Chemistry, 2005, 24(5): 520-524.

甲醛光催化降解与过氧化氢生成的相关性研究

  • 1.  江南大学生物工程学院, 工业生物技术教育部重点实验室, 无锡, 214036;
  • 2.  日本九州工业大学生化工程与科学系, 日本福冈县饭市, 820-8502
基金项目:

江苏省创新人才(学术)项目(No.BK2004401)

摘要: 分别采用两种光催化剂(TiO2与Pd/TiO2)和三种紫外光源(黑光灯、杀菌灯、臭氧灯)分解水溶液中的甲醛,同时以酶法测定光催化降解过程中生成的低浓度过氧化氢.发现波长较短的紫外光源生成过氧化氢的浓度较高.当以臭氧灯为光源时,无论是否有催化剂存在,生成的过氧化氢浓度都在50mmol·m-3以上,因为185nm以下的紫外光可以直接由水与溶解氧生成臭氧,而后生成过氧化氢.不管有无催化剂存在,在臭氧灯作用下,甲醛溶液中生成的过氧化氢浓度高于纯水中生成的过氧化氢浓度.但是,在以黑光灯或臭氧灯为光源时,上述结果正好相反.此外,对于每种光源而言,当采用Pd/TiO2代替TiO2时,甲醛的分解和过氧化氢的生成都得到加强.甲醛光催化分解速率与相同条件下纯水中过氧化氢的生成速率呈正比,表明光催化降解的活性与光催化生成过氧化氢的能力近似呈正相关.

English Abstract

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