期刊文献+

磷钨酸光催化六氟苯脱氟的研究 被引量:4

Photocatalytic Degradation of Hexafluorobenzene by Tungstophosphoric Acid
下载PDF
导出
摘要 选择六氟苯作为目标化合物,利用266 nm脉冲激光照射磷钨酸与六氟苯的混合溶液证实了光催化转化六氟苯的可行性.结果表明,氟离子生成率与光照时间、pH值、磷钨酸初始投加量和添加物的量有关.氟离子生成率随激光脉冲次数的增加而升高.在溶液pH=1.0的条件下,氟离子生成率最高.2.0×10-4mol/L的六氟苯与5.0×10-6mol/L的磷钨酸的混合溶液在接受脉冲激光后,氟离子生成率可达208.1%.外加的氧化剂O2、KMnO4、K2S2O8可以有效氧化还原态的磷钨酸,实现整个光催化循环.溶液中存在的醇类及芳香族有机化合物不利于磷钨酸光催化转化六氟苯. We verified that C6F6, a typical perfluorine compound, could be photocatalytic degraded by H3PW12O40. The defluorination of C6F6 was determined as a function of irradiation time, pH, initial concentration of H3PW12O40, and additives as well. The defluorination of C6F6 increased with the irradiation time. Acid condition, especially pH = 1.0 is preferred. 3 mL solution of 2.0 × 10^-4 mol/L C6F6 and 5.0 × 10^-6 mol/L H3PW12O40 was irradiated for 20 min and the defluorination of C6F6 was equal to 208.1%. 02, KMnO4 and K2S2O6 added in the solution were able to increase the defluorination of C6F6 via oxidating [PW12O40]^4-. The defluorination of C6F6 would decline in the presence of alcohol and aromatic compounds.
出处 《环境科学》 EI CAS CSCD 北大核心 2006年第8期1501-1507,共7页 Environmental Science
基金 国家自然科学基金项目(20377009)
关键词 H3PW12O40 脉冲激光 六氟苯 添加物 tungstophosphoric acid laser hexafluorobenzene additives
  • 相关文献

参考文献26

  • 1Banks R E.Preparations,Properties and Industrial Application of Organofluorine Compounds[M].Chichester:Wiley,1982.
  • 2Martin J W,Mabury S A,Solomon K R,et al.Bioconcentration and tissue distribution of perfluorinated acids in rainbow trout (Oncorhynchus mykiss)[J].Environmental Toxicology Chemistry,2003,22:196~ 204.
  • 3Berthiaume J,Wallace K B.Perfluorooctanoate,perflourooctanesulfonate,and N-ethyl perfluorooctanesulfonamido ethanol; peroxisome proliferation and mitochondrial biogenesis[J].Toxicology Letters,2002,129:23~32.
  • 4Biegel L B,Hurtt M E,Frame S R,et al.Mechanisms of Extrahepatic Tumor induction by peroxisome proliferators in male CD rats[J].Toxicological Sciences,2001,60:44 ~ 55.
  • 5Martin J W,Kannan K,Berger U,et al.Analytical chanllenges hamper perfluoroalkyl research[J].Environmental Science & Technology,2004,248A~255A.
  • 6Hori H,Takano Y,Koike K,et al.Decomposition of environmentally persistent trifluoroacetic acid to fluoride ions by a homogeneous photocatalyst in water[J].Environmental Science & Technology,2003,37:418~422.
  • 7Hori H,Yamamoto A,Kutsuna S.Efficient photochemical decomposition of long-chain perfluorocarboxylic acids by means of an aqueous/liquid CO2 biphasic system[J].Environmental Science & Technology,2005,39(19):7692~7697.
  • 8Hori H,Yamamoto A,Hayakawa E,et al.Efficient decomposition of environmentally persistent perfluorocarboxylic acids by use of persulfate as a photochemical oxidant[J].Environmental Science & Technology,2005,39(7):2383~2388.
  • 9Moriwaki H,Takagi Y,Tanaka M,et al.Sonochemical decomposition of perfluorooctane sulfonate and perfluorooctanoic acid[J].Environmental Science & Technology,2005,39(9):3388~ 3392.
  • 10Minero C,Pelizzetti E,Terzian R,et al.Reactions of hexafluorobenzene and pentafluorophenol catalyzed by irradiated TiO2 in aqueous suspensions[J].Langmuir,1994,10:692~698.

二级参考文献25

  • 1Lipczynska-Kochany,E.;Bolton,J.R.Environ.Sci.Technol.,1992,26:259
  • 2Kochany,J.;Bolton,J.R.Environ.Sci.Technol.,1992,26:262
  • 3Draganic,Z.D.;Draganic,I.G.J.Am.Chem.Soc.,1969,78(8):2571
  • 4Michael,B.D.;Hart,E.J.J.Phys.Chem.,1970,98(15):2878
  • 5Shimo,N.;Nakashima,N.;Yoshihara,K.Bull.Chem.Soc.Jpn.,1983,56:389
  • 6Nakashima,N.;Yoshihara,K.J.Chem.Phys.,1982,77(12):6040
  • 7Yu,X.Y.;Barker,J.R.J.Phys.Chem.A,2003,107(9):1325
  • 8Yu,X.Y.;Barker,J.R.J.Phys.Chem.A,2003,107(9):1313
  • 9Pastia,B.;Laverne,J.A.J.Phys.Chem.,1999,103:1592
  • 10Matheson,M.S.;Mamou,A.;Silverman,J.;Rabani,J.J.Phys.Chem.,1973,77:2420

共引文献5

同被引文献63

  • 1邓谦,吕晓萌,蔡铁军,彭振山,萧菡曦,朱永法.磷钨酸表面修饰TiO_2光催化降解空气污染物[J].中国环境科学,2005,25(3):375-379. 被引量:35
  • 2张芳,李光明,盛怡,胡惠康,王华.电催化氧化法处理苯酚废水的Mn-Sn-Sb/γ-Al_2O_3粒子电极研制[J].化学学报,2006,64(3):235-239. 被引量:27
  • 3郑怀礼,彭德军,李宏,李晓红,王白雪,谢礼国.光助Fenton催化氧化反应降解孔雀石绿试验研究[J].光谱学与光谱分析,2007,27(5):1006-1009. 被引量:23
  • 4Vinod Kumar Gupta, Rajeev Jain, Shaily Varshney. Electrochemical removal of the hazardous dye reactofix red 3BFN from industrial effluents [J]. Journal of Colloid and Interface Science, 2007,312:292-296.
  • 5Eleonora-Mihaela Ungureanu, Alexandru C Razus, Liviu Birzan,et al. Electrochemical study of azo-azulene compounds [J]. Electrochimica, 2008,53:7089-7099.
  • 6Zhong Jun-bo, Ma Di, Zhao Hong, et al. Kinetic study on photocatalytic degradation of reactive orange 5solution with phosphotungstic acid [J]. J Mol Catal A: Chemical, 2008,283: 93 -98.
  • 7Andrea Maldotti, Alessandra Molinari, Rossano Amadelli. Photocatalysis with organized systems for the oxofunetionalization of hydrocarbons by O2 [J]. Chem. Rev., 2002,102:3811- 3836.
  • 8Qu Ping, Zhao Jincai, Shen Tan, et al. TiO2assisted photodegradation of dyes: a study of two competitive primary process in the degradation of RB in an aqueous TiO2 colloidal solution [J]. Journal of Molecular Catalysisi A: Chemical, 1998,129:257-268.
  • 9Anastasia Hiskia, Athanasius Mylonas, Despina Tsipi, et al. Photocatalytic degradation of lindane in aqueous solution [J]. Pestic.Sci., 1997,50:171 - 174.
  • 10Craig L Hill, Donald A Bouchard, Miryam Kadkhodayan, et al. Catalytic photochemical oxidation of organic substrates by polyoxometalates. Picosend spectroscopy, hotoehemistry, and structural properties of charge-transfer eomplexes between hetefopolytungstic acids and dipolar organic compounds [J]. J. Am. Chem. Soc., 1988,110(16):5471-5479.

引证文献4

二级引证文献31

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部