期刊文献+

胶原纤维负载铁Fe(Ⅲ)催化剂对邻苯二甲酸二甲酯的光助催化降解特性 被引量:4

Catalytic degradation of dimethyl phthalate by photo-assisted Fe(Ⅲ) immobilized collagen fiber
下载PDF
导出
摘要 将Fe(Ⅲ)负载在胶原纤维上制备负载型铁催化剂(FeCF),并研究了该催化剂对邻苯二甲酸二甲酯(DMP)的非均相Fenton催化降解性能。结果表明:与FeCF/H2O2/暗光体系、FeCF/UV体系和H2O2/UV体系相比,FeCF/H2O2/UV体系对DMP的降解率明显提高。H2O2用量、反应温度是影响FeCF光助催化降解DMP的两个主要因素。在254nm紫外线照射下,当FeCF和H2O2的用量分别为1.0g.L-1和1.0mmol.L-1时,30min内即可将DMP 100%降解。此外,FeCF的最适pH值范围较宽,为3.07~7.96。FeCF使用5次后其光催化降解能力没有明显降低。因此,FeCF在治理DMP污染方面具有潜在的应用前景。 Fe (Ⅲ) immobilized collagen fiber (FeCF) catalyst was prepared and its photo-assisted catalytic degradation behaviors to dimethyl phthalate (DMP) were investigated. Compared with FeCF/ H2O2/dark, FeCF/UV and H2O2/UV reaction system, FeCF/H2O2/UV is more effective for degradation of DMP. It is found that the H2O2 concentration and temperature are the main factors that greatly influence the degradation performance of DMP. Under irradiation of UV 254 nm, 100% degradation of DMP can be obtained within 30 min when the dosage of FeCF and H2O2 is 1.0 g · L^-1 and 1.0 mmol · L^-1 respectively. In addition, FeCF is effective for the degradation of DMP in the wide pH range of 3.07 to 7.96, and its photo-assisted catalytic degradation activity has no obvious decrease in 5 cycles. So, there is a potential for FeCF to treat DMP pollutant.
出处 《化工学报》 EI CAS CSCD 北大核心 2011年第12期3419-3427,共9页 CIESC Journal
基金 国家自然科学基金项目(20776090)~~
关键词 胶原纤维 负载铁催化剂 邻苯二甲酸二甲酯 UV光助催化降解 collagen fiber Fe(Ⅲ) immobilized catalyst dimethyl phthalate UV assisted degradation
  • 相关文献

参考文献34

  • 1Bauer M J, Herrmann R. Estimation of the environmental contamination hy phthalic acid esters leaching from household wastes [J]. Science of the Total Environment, 1997, 208 (1/2): 49-57.
  • 2Wang P, Wang S L, Fan C Q. Atmospheric distribution of particulateand gas-phase phthalic esters (PAEs) in a Metropolitan City, Nanjing, East China[J]. Chemosphere, 2008, 72 (10):1567-1572.
  • 3Chen J, Liu H, Qiu Z, Shu W. Analysis of di-n-butyl phthalate and other organic pollutants in Chongqing women undergoing parturition [J ]. Environmental Pollution, 2008, 156 (3): 849-853.
  • 4Wang F, Xia X, Sha Y. Distribution of phthalic acid esters in Wuhan section of the Yangtze River, China [J]. Journal of Hazardous Materials, 2008, 154 (1/2/3) 317-324.
  • 5Zeng F, Cui K, Xie Z, Wu L, Liu M, Sun G, Lin Y, Luo D, Zeng Z. Phthalate esters (PAEs) : emerging organic contaminants in agricultural soils in peri-urban areas around Guangzhou, China [J]. Environmental Pollution, 2008, 156 (2): 425-434.
  • 6van Wezel A P, van Vlaardingen P, Posthumus Crommentuijn G H, Sijm D T H M. Environmental limits for two phthalates, with special emphasis R, risk on endocrine disruptive properties [ J ]. Ecotoxicology and Environmental Safety, 2000, 46 (3): 305-321.
  • 7吕怡兵,付强,陈瑛.环境中邻苯二甲酸酯类物质的污染现状与监测方法[J].中国环境监测,2007,23(5):66-70. 被引量:35
  • 8Salima C J, Liu H, Kennedy J F, Comparative study of the adsorption on chitosan beads of phthalate esters and their degradation products [J]. Carbohydrate Polymers, 2010, 81:640-644.
  • 9Stales C A, Peterson D R, Parkerton T F, Adams W J. The environmental fate of phthalate esters: a literature review[J]. Chemosphere, 1997, 35 (4) : 667-749.
  • 10雷乐成,何锋.均相Fenton氧化降解苯酚废水的反应机理探讨[J].化工学报,2003,54(11):1592-1597. 被引量:27

二级参考文献99

共引文献344

同被引文献40

引证文献4

二级引证文献20

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