<p>Chloroquine phosphate (CQP), a widely utilized antimalarial and anti-COVID-19 medication, exhibits persistence and ecotoxicity in aquatic environments. This study systematically investigated the CQP degradation in the UV-activated peroxymonosulfate (UV/PMS) process, focusing on influencing factors, degradation pathways, and constructs the first-principle kinetic model describing this degradation. The UV/PMS process effectively degraded CQP with a pseudo-first-order reaction rate constant of 0.271&#xa0;min<sup>− 1</sup>, sulfate radicals (SO<sub>4</sub>•<sup>−</sup>, 62.4%) and hydroxyl radicals (HO•, 27.3%) were the dominant reactive species. Increasing PMS concentration enhanced radical generation and degradation efficiency. Furthermore, the UV/PMS process exhibited excellent pH adaptability, when the pH value was 10.8, the maximum pseudo-first-order reaction rate constant was 2.894&#xa0;min<sup>− 1</sup> due to the sharp increase in HO• contribution. Cl<sup>−</sup> slightly inhibited degradation by consuming SO<sub>4</sub>•<sup>−</sup>, while HCO<sub>3</sub><sup>−</sup> had no obvious effect due to the non-negligible role of CO<sub>3</sub>•<sup>−</sup>. Additionally, a kinetic model simulated the radical dynamics and degradation trends, showing a strong correlation with experiments. Several potential degradation pathways involved N-deethylation, C-N bond cleavage, hydrogen abstraction, and N-oxidation. An economic analysis revealed that the total cost reached the minimum of 0.33 USD/(m<sup>3</sup>∙order) when the concentration of PMS was 0.14 mM. This study provides theoretical support for UV/PMS-based CQP removal from water.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Kinetic modeling and mechanistic insights into chloroquine phosphate degradation by UV-activated peroxymonosulfate

  • Tongtong Jiang,
  • Yang Li,
  • Mingle Xia,
  • Lin Deng,
  • Changbo Zhang,
  • Rajendra Prasad Singh,
  • Gongde Wu

摘要

Chloroquine phosphate (CQP), a widely utilized antimalarial and anti-COVID-19 medication, exhibits persistence and ecotoxicity in aquatic environments. This study systematically investigated the CQP degradation in the UV-activated peroxymonosulfate (UV/PMS) process, focusing on influencing factors, degradation pathways, and constructs the first-principle kinetic model describing this degradation. The UV/PMS process effectively degraded CQP with a pseudo-first-order reaction rate constant of 0.271 min− 1, sulfate radicals (SO4, 62.4%) and hydroxyl radicals (HO•, 27.3%) were the dominant reactive species. Increasing PMS concentration enhanced radical generation and degradation efficiency. Furthermore, the UV/PMS process exhibited excellent pH adaptability, when the pH value was 10.8, the maximum pseudo-first-order reaction rate constant was 2.894 min− 1 due to the sharp increase in HO• contribution. Cl slightly inhibited degradation by consuming SO4, while HCO3 had no obvious effect due to the non-negligible role of CO3. Additionally, a kinetic model simulated the radical dynamics and degradation trends, showing a strong correlation with experiments. Several potential degradation pathways involved N-deethylation, C-N bond cleavage, hydrogen abstraction, and N-oxidation. An economic analysis revealed that the total cost reached the minimum of 0.33 USD/(m3∙order) when the concentration of PMS was 0.14 mM. This study provides theoretical support for UV/PMS-based CQP removal from water.