2021
DOI: 10.1016/j.cej.2020.127255
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Degradation of spiramycin by thermally activated peroxydisulfate: Kinetics study, oxidation products and acute toxicity

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Cited by 23 publications
(4 citation statements)
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“…Furthermore, it was found that there was a good linear relationship between the natural log of k obs and the reciprocal of the thermodynamic temperature (Figure S18). The apparent activation energy ( E a ) was then calculated as 0.34 kJ mol –1 according to the Arrhenius equation, which was far lower than that of heat-activated PDS (above 85.00 kJ mol –1 ). , The result further demonstrated that the acceleration of the reaction between PDS and ABTS to form reactive species was the major cause for the improvement of DCF degradation with increasing reaction temperature in the PDS/ABTS system.…”
Section: Resultsmentioning
confidence: 94%
See 1 more Smart Citation
“…Furthermore, it was found that there was a good linear relationship between the natural log of k obs and the reciprocal of the thermodynamic temperature (Figure S18). The apparent activation energy ( E a ) was then calculated as 0.34 kJ mol –1 according to the Arrhenius equation, which was far lower than that of heat-activated PDS (above 85.00 kJ mol –1 ). , The result further demonstrated that the acceleration of the reaction between PDS and ABTS to form reactive species was the major cause for the improvement of DCF degradation with increasing reaction temperature in the PDS/ABTS system.…”
Section: Resultsmentioning
confidence: 94%
“…The apparent activation energy (E a ) was then calculated as 0.34 kJ mol −1 according to the Arrhenius equation, which was far lower than that of heat-activated PDS (above 85.00 kJ mol −1 ). 7,55 The result further demonstrated that the acceleration of the reaction between PDS and ABTS to form reactive species was the major cause for the improvement of DCF degradation with increasing reaction temperature in the PDS/ABTS system. Anti-interference Capacity of the PDS/ABTS System.…”
Section: •−mentioning
confidence: 87%
“…Advanced oxidation processes (AOPs) have been reported to effectively degrade an array of recalcitrant organic pollutants via highly reactive oxidants such as hydroxyl radical (•OH) and sulfate radical (SO •− 4 ) [14][15][16][17], among which, SO •− 4 -based AOPs have recently attracted tremendous attention due to their strong oxidation ability and wide reaction pH range [18]. SO •− 4 can be generated from persulfate anion (S 2 O 2− 8 ), as reported in many successful applications of the peroxydisulfate (PDS)-based oxidation process once activated by light, metal ion, or heat [15,19,20].…”
Section: Introductionmentioning
confidence: 99%
“…SO •− 4 can be generated from persulfate anion (S 2 O 2− 8 ), as reported in many successful applications of the peroxydisulfate (PDS)-based oxidation process once activated by light, metal ion, or heat [15,19,20]. Then, in principle, persulfates could be a suitable candidate to be integrated with MD, where the temperature of the feed solution, usually kept at 40-100 • C, could serve as an existing activator for the generation of SO •− 4 [15,18]. The degradation of surfactants using AOPs, especially to mitigate membrane wetting in the MD process, has rarely been investigated.…”
Section: Introductionmentioning
confidence: 99%