高等学校化学学报 ›› 2002, Vol. 23 ›› Issue (6): 1180.

• 研究简报 • 上一篇    下一篇

硝基酚类化合物在海水中的光化学氧化研究

杨桂朋1, 戚佳琳2   

  1. 1. 青岛海洋大学化学化工学院, 青岛 266003;
    2. 山东省商品进出口检验局, 青岛 266002
  • 收稿日期:2001-06-11 出版日期:2002-06-24 发布日期:2002-06-24
  • 通讯作者: 杨桂朋(1963年出生),男,博士,教授,博士生导师,从事海洋化学和环境化学研究.E-mail:gpyang@ees.hokudai.ac.jp E-mail:gpyang@ees.hokudai.ac.jp
  • 基金资助:

    国家自然科学基金(批准号:49706070);山东省自然科学基金(批准号:Q97E04145)资助

Studies on Photochemical Oxidation of Nitrophenols in Seawater

YANG Gui-Peng1, QI Jia-Lin2   

  1. 1. College of Chemistry and Chemical Engineering, Ocean University of Qingdao, Qingdao 266003, China;
    2. Shandong Import and Export Commodity Inspection Bureau, Qingdao 266002, China
  • Received:2001-06-11 Online:2002-06-24 Published:2002-06-24

关键词: 对硝基苯酚, 2, 4-二硝基苯酚, 光化学反应, 海水

Abstract: The photochemical degradation of p-nitrophenol and 2,4-dinitrophenol in both natural seawater and artificial seawater was studied under the irradiation of mixed light sources(ultraviolet lamp/high pressure mercury lamp). The photolysis of the two nitrophenols was influenced by various factors including medium, heavy metal ions and photosensitizer. The photolysis of the two nitrophenols in natural seawater was faster than in artificial seawater, presumably due to the effect of inherent photosensitizers in natural seawater. The addition of Cu2+, Pb2+ or Cd2+ into the seawater solutions obviously increased the photolysis rate of the nitrophenols. Interestingly, we found that the presence of anthroquinone could accelerate the photolysis of p-nitrophenol in natural seawater but had almost no impact on the photolysis of 2,4-dinitrophenol. The half-lives of the photoreactions in natural seawater under our conditions were 40-54 min for p-nitrophenol and 37-69 min for 2,4-dinitrophenol, respectively. Our study suggests that photochemical degradation is an important removal pathway for the nitrophenols in seawater.

Key words: p-Nitrophenol, 2,4-Dinitrophenol, Photochemical oxidation, Seawater

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