4.7 Article

Photolytic and photocatalytic degradation of surface oil from the Deepwater Horizon spill

期刊

CHEMOSPHERE
卷 95, 期 -, 页码 415-422

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2013.09.060

关键词

Photochemistry; Oil spill; Petroleum; Photocatalyst; Remediation

资金

  1. National Science Foundation [CHE-0611902, CHE-1111525]
  2. BP/The Gulf of Mexico Research Initiative via the Northern Gulf Institute [10-BP-GRI-UNO-01]
  3. National Science Foundation Research Experiences for Undergraduates site [DMR-1004869]
  4. Army Research Office via Academy of Applied Science [W911NF-04-1-0226]
  5. Direct For Mathematical & Physical Scien [1262904] Funding Source: National Science Foundation
  6. Division Of Chemistry [1111525] Funding Source: National Science Foundation

向作者/读者索取更多资源

The photochemical behavior of Deepwater Horizon oil collected from the surface of the Gulf of Mexico was studied. Thin oil films on water were subjected to simulated sunlight, and the resulting chemical and optical changes were observed. Polycyclic aromatic hydrocarbons (PAHs) showed substantial photodegradation, with larger PAHs being more rapidly decomposed. About 60% of the fluorescence at the excitation and emission maxima was observed with 12 h of simulated solar irradiation equivalent to approximately 3 d of sunlight. Synchronous scan fluorescence measurements showed 80-90% loss of larger PAHs with 12 h of simulated solar irradiation. Absorbance of the oil decreased by only 20% over the same time period. Alkanes showed no significant photochemical losses. After irradiation, the toxicity of water in contact with the oil significantly increased, presumably due to the release of water soluble photoproducts that were toxic. Photocatalyst addition resulted in enhanced degradation rate for PAHs, and toxicity of the aqueous layer was altered in the presence of photocatalysts added to the oil film. Photochemistry is an important pathway for degradation of large PAHs, which are typically resistant to biodegradation. (C) 2013 Elsevier Ltd. All rights reserved.

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