1999
DOI: 10.1016/s0304-3894(98)00225-8
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Estimation of ⋅OH radical reaction rate constants for phenol and chlorinated phenols using UV/H2O2 photo-oxidation

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Cited by 102 publications
(44 citation statements)
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“…However, the time required for degradation in both the cases is still long (300 min). This is in agreement with the observations of De et al (1999), that the presence of chlorine atoms creates an electron rich atmosphere in the aromatic ring, making it more resistant to hydroxyl radical attack. In Fenton process, the same amount of 2,4,6 T is degraded with in 180 min.…”
Section: Mineralisation Of 246 Tsupporting
confidence: 93%
“…However, the time required for degradation in both the cases is still long (300 min). This is in agreement with the observations of De et al (1999), that the presence of chlorine atoms creates an electron rich atmosphere in the aromatic ring, making it more resistant to hydroxyl radical attack. In Fenton process, the same amount of 2,4,6 T is degraded with in 180 min.…”
Section: Mineralisation Of 246 Tsupporting
confidence: 93%
“…In the presence of an excess mole ratio of H 2 O 2 to phenol, the following additional reactions are likely to occur [33,34]: …”
Section: Kinetic Analysismentioning
confidence: 99%
“…Applying the steady-state approximation [5,8,33,34,39,40] to the transitory reactive intermediates, we can write the following:…”
Section: Kinetic Analysismentioning
confidence: 99%
“…Degradation of phenol by different AOPs, including UVbased processes, has been reported in the literature [8][9][10][11][12][13][14]. It is well known that phenol oxidation treatments lead to the generation of highly toxic intermediate products [1], and there is scarcity of toxicity and environmental impact studies.…”
Section: Introductionmentioning
confidence: 99%