2016
DOI: 10.4067/s0717-97072016000200019
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Hydroxyl Radical Based Degradation of Ciprofloxacin in Aqueous Solution

Abstract: This study reports the degradation of ciprofloxacin (CIP) by means of ionizing radiations. Kinetic studies with aqueous concentrations of 4.6, 10, 15, 17.9 mg/L reveals that degradation of CIP follows pseudo-first order kinetics and the decay constant increased with decrease in initial concentration of CIP. The removal efficiency, represented by G-value, decreased with increasing absorbed dose and increased with higher [CIP] 0 concentration at a given absorbed dose. The effects of bubbling CIP solution with N … Show more

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Cited by 17 publications
(6 citation statements)
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References 23 publications
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“…6a, 7a, 8a, 9a) suggested, in general, highest decomposition (77% to 95%) under saturated N 2 O and at natural pH. The higher degradation under N 2 O atmosphere was previously described [35], being related with the increase of OH radical due to the conversion of …”
Section: Degradation Of Phenolic Acidssupporting
confidence: 50%
“…6a, 7a, 8a, 9a) suggested, in general, highest decomposition (77% to 95%) under saturated N 2 O and at natural pH. The higher degradation under N 2 O atmosphere was previously described [35], being related with the increase of OH radical due to the conversion of …”
Section: Degradation Of Phenolic Acidssupporting
confidence: 50%
“…This result can be explained by the high concentration of hydroxyl radicals formed, leading to great degradation efficiency. 51,52…”
Section: Resultsmentioning
confidence: 99%
“…This result can be explained by the high concentration of hydroxyl radicals formed, leading to great degradation efficiency. 51,52 The inuence of catalyst concentration on the degradation rate of methidathion was investigated by using different concentrations of CuFe 2 O 4 @SiO 2 -GO COOH sonocatalyst. The results of this study are presented in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…In Fricke dosimeter, hydrogen ions are considered as strong scavengers of hydrated electrons [4][5][6]. The effectiveness of a chemical scavenger depends upon the product k[scavenger] that must have a higher value than k[substrate].…”
Section: Competition Kineticsmentioning
confidence: 99%