2017
DOI: 10.1016/j.chemosphere.2016.10.027
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Ibuprofen degradation and toxicity evolution during Fe2+/Oxone/UV process

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Cited by 47 publications
(15 citation statements)
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“…Davide 35 found that both ozonation and UV/H 2 O 2 systems proved to be effective in DCF degradation, ensuring a complete conversion of the chlorine into chloride ions, while degrees of mineralization for ozonation was 32% and 39% for UV/H 2 O 2 after a 90-min treatment. Similar low TOC removal results have been reported in degrading the three NSAIDs using other AOPs, such as UV/H 2 O 2 36 , UV/O 3 37 , and UV/TiO 2 38 . It can be concluded that DPs cannot be mineralized effectively by AOPs, though parent compounds are largely removed.…”
Section: Resultssupporting
confidence: 84%
See 1 more Smart Citation
“…Davide 35 found that both ozonation and UV/H 2 O 2 systems proved to be effective in DCF degradation, ensuring a complete conversion of the chlorine into chloride ions, while degrees of mineralization for ozonation was 32% and 39% for UV/H 2 O 2 after a 90-min treatment. Similar low TOC removal results have been reported in degrading the three NSAIDs using other AOPs, such as UV/H 2 O 2 36 , UV/O 3 37 , and UV/TiO 2 38 . It can be concluded that DPs cannot be mineralized effectively by AOPs, though parent compounds are largely removed.…”
Section: Resultssupporting
confidence: 84%
“… 58 observed that C. carpio exposed to 7 mg/L DCF water was affected in oxidative stress status during the initial days of the study (at 4 days), exhibiting an increased response in blood and liver at 24 days. A higher toxicity of DPs of NSAIDs (NPX 59 , DCF 60 , IBP 37 , 39 ) generated in UV or AOPs were observed using Daphnia magna, Vibrio fisheri as test organisms. According to the biochemical parameters, Group 4 (NSAIDs treated by UV/PS for 30 min) showed more severe oxidative damage than Group 3 (NSAIDs treated by UV/PS for 5 min), suggesting that more toxic DPs were produced as the UV/PS treatment time increased.…”
Section: Resultsmentioning
confidence: 97%
“…Because the samples were taken manually, the first sampling point fell into 10 s–30 min in the literature determining the degradation kinetics of organic contaminants in the Fe­(II)/PMS process, as summarized in Table S1. The researchers have neglected the degradation kinetics of organic contaminants in the Fe­(II)/PMS process before the first sampling point, although most of the organic contaminants were decomposed in this stage. , , For instance, one study displayed that 74.2% of 2-chlorobiphenyl was degraded within 30 min (the first sampling time) in the Fe­(II)/PMS process and only 23.6% of 2-chlorobiphenyl was further oxidized in the following 3.5 h . Therefore, it could be inferred that the degradation rate of organic contaminants in the rapid oxidation stage was greatly underestimated in the literature.…”
Section: Introductionmentioning
confidence: 99%
“…In the single Fe 2+ and single UV lacking in oxidant, the main contribution to the removal of organics was iron colloids or UV light. 37,38 In single H 2 O 2 without catalysis, ROS production was limited. Hence, the single process cannot achieve a satisfactory treatment results for the above reasons.…”
Section: Resultsmentioning
confidence: 99%