Chenyang Song, Junfeng Li, Zhaoyang Wang, Lijuan Yi, Xi Xie, Wenhuai Wang, Qiong Feng, Zhiheng Cao
{"title":"紫外光活化过硫酸盐体系中对乙酰氨基酚自由基和非自由基氧化降解:PDS和PMS的比较。","authors":"Chenyang Song, Junfeng Li, Zhaoyang Wang, Lijuan Yi, Xi Xie, Wenhuai Wang, Qiong Feng, Zhiheng Cao","doi":"10.1080/09593330.2025.2471048","DOIUrl":null,"url":null,"abstract":"<p><p>Due to differences in physical and chemical properties, peroxymonosulfate (PMS) and peroxydisulfate (PDS) show distinct reactivity under ultraviolet (UV) activation. Consequently, selecting the appropriate persulfate concentration is critical for optimising the degradation efficiency of the system. This study compared the degradation efficiency of acetaminophen (ACE) in UV light-activated PDS (UV/PDS) and PMS (UV/PMS) systems. Under optimal conditions ([ACE]<sub>0</sub> = 10 mg·L<sup>-1</sup>, UV light power = 6 W, [pH]<sub>0</sub> = 7), the ACE removal rate reached 97.8% within 60 min when the dosage of PDS was 8 mM. 91.7% within 60 min with 10 mM PMS in the UV/PMS system, and only 82.4% when the PMS dosage was 8 mM. Quenching experiments and electron paramagnetic resonance (EPR) analysis revealed that the UV/PDS system exhibited higher characteristic peak signal intensities for sulfate radical (<math><mi>S</mi><msubsup><mi>O</mi><mn>4</mn><mrow><mo>⋅</mo><mo>-</mo></mrow></msubsup></math>), superoxide radical (<math><msubsup><mi>O</mi><mn>2</mn><mrow><mo>⋅</mo><mo>-</mo></mrow></msubsup></math>), singlet oxygen (<sup>1</sup>O<sub>2</sub>), and hydroxyl radical (<math><mi>OH</mi><mo>⋅</mo></math>) compared to the UV/PMS system. In the UV/PDS system, <math><mi>S</mi><msubsup><mi>O</mi><mn>4</mn><mrow><mo>⋅</mo><mo>-</mo></mrow></msubsup></math> and <sup>1</sup>O<sub>2</sub> were identified as the primary contributors to ACE removal, whereas <math><mi>S</mi><msubsup><mi>O</mi><mn>4</mn><mrow><mo>⋅</mo><mo>-</mo></mrow></msubsup></math> was the predominant species in the UV/PMS system. Moreover, the intermediate products generated during the UV/PDS reaction were analyzed using liquid chromatography-mass spectrometry (LC-MS). This study demonstrated the feasibility of UV light-activated persulfate systems for ACE treatment, providing a systematic comparison of the performance and mechanisms of ACE degradation between the two systems. The findings offer valuable insights and practical guidance for selecting persulfates in UV light-activated research and applications.</p>","PeriodicalId":12009,"journal":{"name":"Environmental Technology","volume":" ","pages":"3571-3588"},"PeriodicalIF":2.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Radical and nonradical oxidative degradation of acetaminophen in ultraviolet light activated persulfate systems: comparison of PDS and PMS.\",\"authors\":\"Chenyang Song, Junfeng Li, Zhaoyang Wang, Lijuan Yi, Xi Xie, Wenhuai Wang, Qiong Feng, Zhiheng Cao\",\"doi\":\"10.1080/09593330.2025.2471048\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Due to differences in physical and chemical properties, peroxymonosulfate (PMS) and peroxydisulfate (PDS) show distinct reactivity under ultraviolet (UV) activation. Consequently, selecting the appropriate persulfate concentration is critical for optimising the degradation efficiency of the system. This study compared the degradation efficiency of acetaminophen (ACE) in UV light-activated PDS (UV/PDS) and PMS (UV/PMS) systems. Under optimal conditions ([ACE]<sub>0</sub> = 10 mg·L<sup>-1</sup>, UV light power = 6 W, [pH]<sub>0</sub> = 7), the ACE removal rate reached 97.8% within 60 min when the dosage of PDS was 8 mM. 91.7% within 60 min with 10 mM PMS in the UV/PMS system, and only 82.4% when the PMS dosage was 8 mM. Quenching experiments and electron paramagnetic resonance (EPR) analysis revealed that the UV/PDS system exhibited higher characteristic peak signal intensities for sulfate radical (<math><mi>S</mi><msubsup><mi>O</mi><mn>4</mn><mrow><mo>⋅</mo><mo>-</mo></mrow></msubsup></math>), superoxide radical (<math><msubsup><mi>O</mi><mn>2</mn><mrow><mo>⋅</mo><mo>-</mo></mrow></msubsup></math>), singlet oxygen (<sup>1</sup>O<sub>2</sub>), and hydroxyl radical (<math><mi>OH</mi><mo>⋅</mo></math>) compared to the UV/PMS system. In the UV/PDS system, <math><mi>S</mi><msubsup><mi>O</mi><mn>4</mn><mrow><mo>⋅</mo><mo>-</mo></mrow></msubsup></math> and <sup>1</sup>O<sub>2</sub> were identified as the primary contributors to ACE removal, whereas <math><mi>S</mi><msubsup><mi>O</mi><mn>4</mn><mrow><mo>⋅</mo><mo>-</mo></mrow></msubsup></math> was the predominant species in the UV/PMS system. Moreover, the intermediate products generated during the UV/PDS reaction were analyzed using liquid chromatography-mass spectrometry (LC-MS). This study demonstrated the feasibility of UV light-activated persulfate systems for ACE treatment, providing a systematic comparison of the performance and mechanisms of ACE degradation between the two systems. The findings offer valuable insights and practical guidance for selecting persulfates in UV light-activated research and applications.</p>\",\"PeriodicalId\":12009,\"journal\":{\"name\":\"Environmental Technology\",\"volume\":\" \",\"pages\":\"3571-3588\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental Technology\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1080/09593330.2025.2471048\",\"RegionNum\":4,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/4 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Technology","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1080/09593330.2025.2471048","RegionNum":4,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/4 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Radical and nonradical oxidative degradation of acetaminophen in ultraviolet light activated persulfate systems: comparison of PDS and PMS.
Due to differences in physical and chemical properties, peroxymonosulfate (PMS) and peroxydisulfate (PDS) show distinct reactivity under ultraviolet (UV) activation. Consequently, selecting the appropriate persulfate concentration is critical for optimising the degradation efficiency of the system. This study compared the degradation efficiency of acetaminophen (ACE) in UV light-activated PDS (UV/PDS) and PMS (UV/PMS) systems. Under optimal conditions ([ACE]0 = 10 mg·L-1, UV light power = 6 W, [pH]0 = 7), the ACE removal rate reached 97.8% within 60 min when the dosage of PDS was 8 mM. 91.7% within 60 min with 10 mM PMS in the UV/PMS system, and only 82.4% when the PMS dosage was 8 mM. Quenching experiments and electron paramagnetic resonance (EPR) analysis revealed that the UV/PDS system exhibited higher characteristic peak signal intensities for sulfate radical (), superoxide radical (), singlet oxygen (1O2), and hydroxyl radical () compared to the UV/PMS system. In the UV/PDS system, and 1O2 were identified as the primary contributors to ACE removal, whereas was the predominant species in the UV/PMS system. Moreover, the intermediate products generated during the UV/PDS reaction were analyzed using liquid chromatography-mass spectrometry (LC-MS). This study demonstrated the feasibility of UV light-activated persulfate systems for ACE treatment, providing a systematic comparison of the performance and mechanisms of ACE degradation between the two systems. The findings offer valuable insights and practical guidance for selecting persulfates in UV light-activated research and applications.
期刊介绍:
Environmental Technology is a leading journal for the rapid publication of science and technology papers on a wide range of topics in applied environmental studies, from environmental engineering to environmental biotechnology, the circular economy, municipal and industrial wastewater management, drinking-water treatment, air- and water-pollution control, solid-waste management, industrial hygiene and associated technologies.
Environmental Technology is intended to provide rapid publication of new developments in environmental technology. The journal has an international readership with a broad scientific base. Contributions will be accepted from scientists and engineers in industry, government and universities. Accepted manuscripts are generally published within four months.
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