研究报告

  • 段书乐,马婧捷,党宁,黄艳超,董慧峪,侯嫔,强志民.紫外高级氧化工艺降解水溶液中的人工甜味剂[J].环境科学学报,2020,40(12):4289-4296

  • 紫外高级氧化工艺降解水溶液中的人工甜味剂
  • Oxidation of artificial sweetener in aqueous solution by ultraviolet advanced oxidation processes
  • 基金项目:国家自然科学基金(No.51525806,51878648);北京城市学院2019年度实培计划项目
  • 作者
  • 单位
  • 段书乐
  • 1. 中国矿业大学(北京), 化学与环境工程学院, 北京 100083;2. 中国科学院生态环境研究中心, 中国科学院饮用水科学与技术重点实验室, 北京 100085
  • 马婧捷
  • 北京城市学院, 城市建设学部, 北京 100191
  • 党宁
  • 中国矿业大学(北京), 化学与环境工程学院, 北京 100083
  • 黄艳超
  • 北京城市学院, 城市建设学部, 北京 100191
  • 董慧峪
  • 中国科学院生态环境研究中心, 中国科学院饮用水科学与技术重点实验室, 北京 100085
  • 侯嫔
  • 中国矿业大学(北京), 化学与环境工程学院, 北京 100083
  • 强志民
  • 中国科学院生态环境研究中心, 中国科学院饮用水科学与技术重点实验室, 北京 100085
  • 摘要:人工甜味剂(ASs)作为一类新兴污染物在世界范围内的各种水体中被广泛检出,本文选取具有代表性的糖精(SAC)作为研究对象,探讨了紫外/过氧化氢(UV/H2O2)和UV/过硫酸盐(PS)两种高级氧化工艺(AOPs)降解SAC的动力学、影响因素、矿化率、转化产物和降解机制.结果表明:单独的UV、PS和H2O2对SAC的去除效果有限(去除率<5%),UV/H2O2和UV/PS工艺对SAC的去除效果良好(去除率>99%)且降解符合伪一阶动力学,速率分别为0.38 min-1和0.09 min-1.降低溶液pH值、增大PS浓度均可促进SAC降解;但随着H2O2浓度的升高,SAC降解效率先增加后减小.相比UV/PS工艺,UV/H2O2工艺降解SAC的矿化率更高(可达43%).产物鉴定结果表明,两种UV-AOPs氧化降解SAC均会生成开环产物,表明反应会破坏SAC分子中的N—S结构.此外,UV/H2O2工艺更易生成羟基化产物,二聚体产物仅在UV/PS工艺中被检测到.
  • Abstract:Artificial sweeteners (ASs), are a class of emerging pollutants, which are widely detected in various water samples around the world. Using saccharin (SAC) as the representative ASs, the kinetics, influencing factor, mineralization rate, degradation products and mechanisms by ultraviolet/hydrogen peroxide (UV/H2O2) and UV/persulfate (PS) were investigated in this study. The results showed that the removals of SAC by UV, PS and H2O2 alone were limited (<5%), but exhibited significant removal (>99%) in UV/H2O2 and UV/PS processes. The pseudo-first-order degradation rates of SAC were determined to be 0.38 min-1 and 0.09 min-1 in UV/H2O2 and UV/PS processes, respectively. Both decreasing solution pH and increasing PS dosage enhanced the oxidation of SAC significantly. However, the degradation of SAC increased first and then decreased with increasing initial H2O2 concentration. Compared with UV/PS process, UV/H2O2 process degraded SAC with higher mineralization rate (up to 43%). The ring-opening products of SAC were observed in both UV-based processes, indicating that the N—S structure in the SAC molecule was damaged after the oxidation. In addition, the hydroxylated products were prone to form in UV/H2O2 process, and the dimer product was only observed in UV/PS process.

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