کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
150101 456444 2012 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Efficient degradation of perfluorooctanoic acid by UV–Fenton process
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
Efficient degradation of perfluorooctanoic acid by UV–Fenton process
چکیده انگلیسی

Decomposition of perfluorooctanoic acid (PFOA) was investigated in UV–Fenton systems. It was found that PFOA could be efficiently degraded in the UV–Fenton system, producing fluoride ions and short-chain perfluorinated carboxylic acids. The degradation of PFOA could be divided into two stages: Within reaction time of 1 h, the added PFOA was rapidly degraded, resulting in a PFOA removal of 87.9% and a defluorination efficiency of 35.8%; Beyond 1 h, the PFOA removal was slowly increased to more than 95% at reaction time of 5 h, along with the defluorination efficiency of 53.2%. This corresponded to a two-stage mechanism for the PFOA degradation process in the UV–Fenton system. The fast defluorination and degradation of PFOA at the first stage was attributed to the generation of strong oxidizing OH radicals, which accelerated PFOA decarboxylation. At the second stage, H2O2 was completely consumed, and the defluorination was mainly due to the interactions between PFOA and Fe3+ ions.

The degradation and decarboxylation of PFOA in UV–Fenton system proceeds through two pathways: attacking from the generated OH radicals and decomposing originated from the electron transfer interactions between PFOA and the generated Fe3+ ions.Figure optionsDownload as PowerPoint slideHighlights
► It was confirmed that hydroxyl radicals could decompose PFOA.
► An efficient UV–Fenton approach was proposed for the degradation of PFOA.
► The degradation intermediates of PFOA were short-chain PFCs and fluoride ions.
► A two-stage mechanism was proposed for the UV–Fenton degradation of PFOA.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Chemical Engineering Journal - Volume 184, 1 March 2012, Pages 156–162
نویسندگان
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