[1] Huang C P, Dong C, Tang Z. Advanced chemical oxidation:its presentrole and potential future in hazardous waste treatment[J].Waste Manage, 1993, 13(5/6/7):361-377.
[2] Rahhal S, Richter H W. Reduction of hydrogen peroxide by the ferrousion chelate of diethylenetriamine-N, N, N’, N’’, N’’-pentaacetate[J]. J. Am. Chem. Soc., 1988, 110:3126-3133.
[3] Rush J D, Koppenol W H. Oxidizing intermediates in the reaction offerrous EDTA with hydrogen peroxide[J]. J. Boil. Chem., 1986, 261(15):6730-6733.
[4] Watts R J, Dilly S E. Evaluation of iron catalysts for the Fenton-likeremediation of diesel contaminated soils [J]. J. Hazard. Mater., 1996, 51(1):209-224.
[5] Zepp R G, Faust B C, Hoign J. Hydroxyl radical formation inaqueous reactions(pH:3-8) of iron(Ⅱ) with hydrogen peroxide:the photo-Fenton reaction[J]. Environ. Sci. Technol., 1992, 26(2):313-319.
[6] Malik P K. Oxidation of safranine T in aqueous solution using Fenton’sreagent:Involvement of a Fe(Ⅲ) chelate in the catalytic hydrogenperoxide oxidation of safranine T[J]. J. Phys. Chem. A, 2004, 108(14):2675-2681.
[7] Fukushima M, Tatsumi K, Morimoto K. The fate of aniline after aphoto-Fenton reaction in an aqueous system containing iron(Ⅲ), humic acid, and hydrogen peroxide[J]. Environ. Sci. Technol., 2000, 34(10):2006-2013.
[8] Fukushima M, Sawada A, Kawasaki M, et al. Influence of humicsubstances on the removal of pentachlorophenol by a biomimeticcatalytic system with a water-soluble iron(Ⅲ)-porphyrin complex[J]. Environ. Sci. Technol., 2003, 37(5):1031-1036.
[9] Fukushima M, Tatsumi K. Effect of hydroxypropyl-β-cyclo-dextrinon the degradation of pentachlorophenol by potassium monopersulfatecatalyzed with Iron(Ⅲ)-porphyrin complex[J]. Environ. Sci.Technol., 2005, 39(23):9337-9342.
[10] Paciolla M D, Davies G, Jansen S A. Generation of hydroxyl radicalsfrom metal-loaded humic acids [J]. Environ. Sci. Technol., 1999, 33(11):1814-1818.
[11] Sun Y, Pignatello J J. Activation of hydrogen peroxide by iron(Ⅲ)chelates for abiotic degradation of herbicides and insecticides inwater[J]. J. Agric. Food Chem., 1993, 41(2): 308-312.
[12] Howsawkeng J, Watts R J, Washington D L, et al. Evidence for simultaneousabiotic-biotic oxidations in a microbial-Fenton’s system[J]. Environ. Sci. Technol., 2001, 35(14):2961-2966.
[13] Hughes M N. The inorganic chemistry of biological process[M]. 2th ed. New York:John Wiley Sons, 1972:118.
[14] Everse J, Everse K E, Grisham M B. Peroxidases in chemistry andbiology(VolumeⅡ)[M]. CRC:Boca Raton, FL, 1991:156.
[15] Moss T H, Ehrenberg A, Bearden A. M觟ssbauer spectroscopic evidencefor the electronic configuration of iron in horseradish peroxidaseand its peroxide derivatives[J]. Biochem. , 1969 , 8(10) :4159-4162.
[16] Balch A L, Chan Y W, Cheng R J, et al. Oxygenation patterns foriron(Ⅱ) porphyrins peroxo and ferryl[Fe(Ⅳ)O] intermediatesdetected by 1H nuclear magnetic resonance spectroscopy during theoxygena tion of (tetramesityl-porphyrin) iron(Ⅱ)[J]. J. Am.Chem. Soc., 1984, 106(25) :7779-7785.
[17] Harami T, Maeda Y, Morita Y, et al. M?ssbauer spectroscopic determinationof the electronic structure of highly oxidized iron inhemoproteins[J]. J. Chem. Phys., 1977, 67(3):1164-1169.
[18] Sitter A J, Reczek C M, Terner J. Observation of the Fe(Ⅳ)O stretching vibration of ferryl myoglobin by resonance Raman spectroscopy[J]. Biochim. Bio phys. Acta., 1985, 828 (3):229 -235.
[19] Tao X, Ma W, Zhang T, et al. Efficient oxidative degradation of organicpollutants in the presence of iron tetrasulfophthalayanine undervisible irradiation[J]. Angew. Chem. Int. Ed., 2001, 113:3013.
[20] Tao X, Ma W, Zhang T, et al. A novel approach for the oxidativedegradation of organic pollutants in aqueous solutions mediated byiron tetrasulfophthalayanine under visible light radiation[J].Chem. Eur. J., 2002, 8(6):1321-1326.
[21] 高冠道, 陈金龙, 费正皓, 等. 超高交联树脂催化剂对水溶液中孔雀绿的催化降解研究[J]. 高分子学报, 2006(1):113-117.
[22] Collins T J, Kostka K L, Munck E, et al. Stabilization of mononuclearfive-coordinate iron(Ⅳ)[J]. J. Am. Chem. Soc., 1990, 112(14): 5637-5639.
[23] Gupta S S, Stadler M, Noser C A, et al. Rapid total destructionchlorophenols by activated hydrogen peroxide [J]. Science, 2002, 296(5566):326-328.
[24] Ciardelli F, Carlini C, Pertici P, et al. Polymer effect on catalysis bymacromolecules/transition metal complexes[J]. J. Macromol. Sci.A, 1989, 26(2/3):327-329.
[25] Ingham S L, Long N J. The first metal complexes with a doubly S3-bridged ferrocene ligand[J]. Angew. Chem. Int. Ed. Engl., 1994, 33(17):1752-1753.
[26] 王贤保, 陈正国, 程时远. 高分子金属络合物的性能及应用进展[J]. 高分子材料科学与工程, 2000, 16(4):8-12.
[27] Parton R F, Neys P E, Jacobs P A, et al. Iron-phthalocyanine im-mobilized on activated carbon black: a selective catalyst for alkaneoxidation[J]. J. Catal. , 1996, 164(2):341-346.
[28] Fernandez J, Bandara J, Lopez A, et al. Photoassisted Fentondegradation of nonbiodegradable azo dye(Orange Ⅱ) in Fe-freesolutions mediated by cation transfer membranes[J]. Langmuir, 1999, 15(1):185-192.
[29] Fernandez J, Bandara J, Kiwi J, et al. Efficient photo-assisted Fentoncatalysis mediated by Fe ions on Nafion membranes active inthe abatement of non-biodegradable azo dye[J]. Chem. Commun., 1998(14):1493-1494.
[30] Kiwi J, Denisov N, Gak Y, et al. Catalytic Fe3+ clusters and complexesin Nafion active in photo-Fenton processes. High-resolutionelectron microscopy and femtosecond studies[J]. Langmuir, 2002, 18(23):9054-9066.
[31] Héquet V, Le C P, Gonzalez C, et al. Photocatalytic degradation ofatrazine by porphyrin and phthalocyanine complexes[J]. Chemosphere, 2000, 41(3):379-386.
[32] Mukherjee M, Ray A R. Biomimetic oxidation of L-arginine withhydrogen peroxide catalyzed by the resin-supported iron(Ⅲ) porphyrin[J]. J. Mol. Catal. A:Chem., 2007, 266(1/2):207-214.
[33] Liou R M, Chen S H, Hung M Y, et al. Fe(Ⅲ) supported on resinas effective catalyst for the heterogeneous oxidation of phenol inaqueous solution[J]. Chemosphere, 2005, 59(1):117-125.
[34] 张瑛洁, 马军, 姚军, 等. 可见光多相类Fenton降解水中孔雀石绿[J]. 哈尔滨工业大学学报, 2010, 42(4):1569-1572.
[35] 张瑛洁, 马军, 陈雷, 等. 树脂负载草酸铁光助类Fenton降解水中孔雀石绿[J]. 环境科学, 2009, 30(12):3609-3613.
[36] 张瑛洁, 马军, 宋磊, 等. 树脂负载Fe3+/Cu2+多相类Fenton降解染料橙黄Ⅳ[J]. 环境科学学报, 2009, 9(7):1419-1425.
[37] 张瑛洁, 马军, 张亮, 等. 树脂负载Fe(Ⅲ)F催化过氧化氢降解染料孔雀石绿[J]. 环境科学学报, 2009, 29(10):2063-2069.
[38] Koppenol W H, Liebman J F. The oxidizing nature of the hydroxylradical. A comparison with the ferryl iron (FeO2+)[J]. J. Phys.Chem., 1984, 88(1): 99-101.
[39] Wink D A, Nims R W, Saavedra J E, et al. The Fenton oxidationmechanism:reactivities of biologically relevant substrates with twooxidizing intermediates differ from those predicted for the hydroxylradical[J]. Proc. Natl. Acad. Sci. , 1994, 91(14):6604-6608.
[40] Bossmann S H, Oliveros E, G?b S, et al. New evidence agaist hydroxylradicals as reactive intermediates in the thermal and photochemicallyenhanced Fenton reactions[J]. J. Phys. Chem. A, 1998, 102(28):5542-5550.
[41] Sheu C, Sobkowiak A, Zhang L, et al. Iron-hydroperoxide inducedphenylselenization of hydrocarbons (Fenton chemistry)[J]. J. Am.Chem. Soc., 1989, 111(20):8030-8032.
[42] Tung H C, Kang C, Sawyer D T. Nature of the reactive intermediatesfrom the iron-induced activation of hydrogen peroxide: agentsfor the ketonization of methylenic carbon, the monooxygenation ofhydrocarbons , and the dioxygenation of arylolefins[J]. J. Am.Chem. Soc., 1992, 114(9):3445-3455.
[43] Sawyer D T, Kang C, Llobet A, et al. Fenton reagents [1∶1 Fe(Ⅱ)Lx/HOOH] react via [LxFe(Ⅱ)OOH(BH+)](1) as hydroxylases(RH→ROH), not as generations of free hydroxyl radicals (HO)[J]. J. Am. Chem. Soc., 1993, 115:5817-5818.
[44] Hage J P, Llobet A, Sawyer D T. Aromatic hydroxylation by Fentonreagents {reactive intermediate [Lx+Fe(Ⅱ)OOH(BH+)], not freehydroxyl radical(HO)}[J]. Bioorg. Med. Chem., 1995, 3 (10):1383-1388.
[45] Sawyer D T, Sobkowiak A, Matsushita T. Metal [MLx;M=Fe, Cu, Co, Mn]/hydroperoxide-induced activation of dioxygen for the oxygenationof hydrocarbon:oxygenated Fenton chemistry[J]. Acc.Chem. Res., 1996, 29:409-416.
[46] Macfaul P A, Wayner D D M, Ingold K U. A radical account of oxygenated Fenton chemistry[J]. Acc. Chem. Res., 1998, 31:159-162.
[47] Walling C. Fenton’agentrevisited[J]. Acc. Chem. Res., 1975, 8:125-131.
[48] Walling C. Intermediates in the reaction of Fenton type reagents[J]. Acc. Chem. Res. , 1998, 31:155-157.
[49] Goldstein S, Meyerstein D. Comments on the mechanism of the Fenton-like reaction[J]. Acc. Chem. Res., 1999, 32:547-550.
[50] Yamazaki I, Piette L H. EPR spin-trapping study on the oxidizingspecies formed in the reaction of the ferrous ion with hydrogen peroxide[J]. J. Am. Chem. Soc., 1991, 113(20):7588-7593.
[51] Zhang Yingjie, Ma Jun, Liu Xusheng, et al. Reactive species inresin supported heterogeneous Fenton-like oxidation of malachitegreen solution[J]. Journal of Harbin Institute of Technology, 2010, 17(2):99-105.
[52] 张瑛洁, 马军, 赵吉, 等. 树脂负载高价铁催化H2O2降解染料橙黄Ⅳ[J]. 哈尔滨工业大学学报, 2010, 42(4):1569-1572. |