
Advanced oxidation of pharmaceuticals by the ozone-activated peroxymonosulfate process : the role of different oxidative species
- Author
- Emma Deniere, Stijn Van Hulle (UGent) , Herman Van Langenhove (UGent) and Kristof Demeestere (UGent)
- Organization
- Abstract
- Given the need for innovations in advanced oxidation processes to deal with challenges such as center dot OH scavenging, this paper addresses the removal of pharmaceuticals with a large variety in ozone reactivity (k(O3) = 0.15-3 x 10(5) M-1 s(-1)) by use of the novel ozone -activated peroxymonosulfate (O-3/PMS) process. A clear improvement in removal efficiency (up to 5 times higher) is noticed as a result of the generation of SO4 center dot-radicals, mainly for slow-ozone reacting compounds (k(O3) <= 250 M-1 s(-1)) and in the presence of a center dot OH scavenger. Depending on the target compound, SO4 center dot-are assessed to contribute for 50-90% to the overall removal of the micropollutants, both in single-compound and mixture experiments. Ozone-based PMS activation occurs at neutral to alkaline pH and, in the presence of a center dot OH scavenger, removal efficiencies during O-3/PMS are up to 3 times higher than with the O-3/H2O2 process. In optimizing the O-3/PMS process, a trade-off has to made between the desired removal and the PMS:O-3 ratio. A molar ratio of 1:10 already results in a clear benefit compared to the ozonation process. Further increase of the PMS content up to a 1:1 ratio improved the removal by an additional factor of 1.3-1.5.
- Keywords
- Advanced oxidation process, Ozone, Peroxymonosulfate, Sulfate radicals, Pharmaceuticals, WASTE-WATER TREATMENT, PARA-CHLOROBENZOIC ACID, DRINKING-WATER, MICROPOLLUTANT ELIMINATION, CHEMICAL OXIDATION, HYDROXYL RADICALS, TREATMENT PLANTS, ORGANIC-MATTER, OZONATION, DEGRADATION
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8583254
- MLA
- Deniere, Emma, et al. “Advanced Oxidation of Pharmaceuticals by the Ozone-Activated Peroxymonosulfate Process : The Role of Different Oxidative Species.” JOURNAL OF HAZARDOUS MATERIALS, vol. 360, 2018, pp. 204–13, doi:10.1016/j.jhazmat.2018.07.071.
- APA
- Deniere, E., Van Hulle, S., Van Langenhove, H., & Demeestere, K. (2018). Advanced oxidation of pharmaceuticals by the ozone-activated peroxymonosulfate process : the role of different oxidative species. JOURNAL OF HAZARDOUS MATERIALS, 360, 204–213. https://doi.org/10.1016/j.jhazmat.2018.07.071
- Chicago author-date
- Deniere, Emma, Stijn Van Hulle, Herman Van Langenhove, and Kristof Demeestere. 2018. “Advanced Oxidation of Pharmaceuticals by the Ozone-Activated Peroxymonosulfate Process : The Role of Different Oxidative Species.” JOURNAL OF HAZARDOUS MATERIALS 360: 204–13. https://doi.org/10.1016/j.jhazmat.2018.07.071.
- Chicago author-date (all authors)
- Deniere, Emma, Stijn Van Hulle, Herman Van Langenhove, and Kristof Demeestere. 2018. “Advanced Oxidation of Pharmaceuticals by the Ozone-Activated Peroxymonosulfate Process : The Role of Different Oxidative Species.” JOURNAL OF HAZARDOUS MATERIALS 360: 204–213. doi:10.1016/j.jhazmat.2018.07.071.
- Vancouver
- 1.Deniere E, Van Hulle S, Van Langenhove H, Demeestere K. Advanced oxidation of pharmaceuticals by the ozone-activated peroxymonosulfate process : the role of different oxidative species. JOURNAL OF HAZARDOUS MATERIALS. 2018;360:204–13.
- IEEE
- [1]E. Deniere, S. Van Hulle, H. Van Langenhove, and K. Demeestere, “Advanced oxidation of pharmaceuticals by the ozone-activated peroxymonosulfate process : the role of different oxidative species,” JOURNAL OF HAZARDOUS MATERIALS, vol. 360, pp. 204–213, 2018.
@article{8583254, abstract = {{Given the need for innovations in advanced oxidation processes to deal with challenges such as center dot OH scavenging, this paper addresses the removal of pharmaceuticals with a large variety in ozone reactivity (k(O3) = 0.15-3 x 10(5) M-1 s(-1)) by use of the novel ozone -activated peroxymonosulfate (O-3/PMS) process. A clear improvement in removal efficiency (up to 5 times higher) is noticed as a result of the generation of SO4 center dot-radicals, mainly for slow-ozone reacting compounds (k(O3) <= 250 M-1 s(-1)) and in the presence of a center dot OH scavenger. Depending on the target compound, SO4 center dot-are assessed to contribute for 50-90% to the overall removal of the micropollutants, both in single-compound and mixture experiments. Ozone-based PMS activation occurs at neutral to alkaline pH and, in the presence of a center dot OH scavenger, removal efficiencies during O-3/PMS are up to 3 times higher than with the O-3/H2O2 process. In optimizing the O-3/PMS process, a trade-off has to made between the desired removal and the PMS:O-3 ratio. A molar ratio of 1:10 already results in a clear benefit compared to the ozonation process. Further increase of the PMS content up to a 1:1 ratio improved the removal by an additional factor of 1.3-1.5.}}, author = {{Deniere, Emma and Van Hulle, Stijn and Van Langenhove, Herman and Demeestere, Kristof}}, issn = {{0304-3894}}, journal = {{JOURNAL OF HAZARDOUS MATERIALS}}, keywords = {{Advanced oxidation process,Ozone,Peroxymonosulfate,Sulfate radicals,Pharmaceuticals,WASTE-WATER TREATMENT,PARA-CHLOROBENZOIC ACID,DRINKING-WATER,MICROPOLLUTANT ELIMINATION,CHEMICAL OXIDATION,HYDROXYL RADICALS,TREATMENT PLANTS,ORGANIC-MATTER,OZONATION,DEGRADATION}}, language = {{eng}}, pages = {{204--213}}, title = {{Advanced oxidation of pharmaceuticals by the ozone-activated peroxymonosulfate process : the role of different oxidative species}}, url = {{http://doi.org/10.1016/j.jhazmat.2018.07.071}}, volume = {{360}}, year = {{2018}}, }
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