...
首页> 外文期刊>Water Science and Technology >Oxidation of sulfamethoxazole by UVA radiation and modified Fenton reagent: toxicity and biodegradability of by-products
【24h】

Oxidation of sulfamethoxazole by UVA radiation and modified Fenton reagent: toxicity and biodegradability of by-products

机译:UVA辐射和改性Fenton试剂氧化磺胺甲恶唑:副产物的毒性和生物降解性

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Improvement of sulfamethoxazole (4-amino-N-(5-methylisoxazol-3-yl)-benzenesulfonamide-SMX) biodegradability using a modified Fenton's reaction has been studied. The modification consists of replacing hydrogen peroxide with atmospheric air and adding copper sulphate as a reaction promoter. Two series of experiments were carried out. The first (Series 1) was conducted using only the catalysts with aeration. In the second series (Series 2), cycles of UVA radiation and aeration were used. During UVA radiation, the removal of sulfamethoxazole proceeds less rapidly than in only aerated solution. After 1.5 h of these two processes, the SMX degradation was 23% in Series 2 and 59% in Series 1. The opposite trend was observed for mineralization and the removal of DOC was about 5% higher in Series 2 than in Series 1. The FTIR spectra of the extracts of reaction products yielded by four organic solvents of varying polarity revealed a wide diversity of functional groups in the post-reaction mixture in comparison to the extracts from sulfamethoxazole solution. Based on FTIR analysis, several oxidation products of sulfamethoxazole are proposed. Apparently, hydroxyl radicals initially attack sulphonamide bonds, resulting in the formation of sulfanilic acid and 3-amino-5-methylisoxazole. Irrespective of the reference organism used in toxicity tests, the post-reaction mixture in the Series 2 was more toxic than the post-reaction mixture in Series 1. In contrast, the biodegradability calculated as BOD5/DOC ratio, was higher for post-reaction mixture 2 and amounted to 0.43.
机译:研究了使用改良的Fenton反应改善磺胺甲恶唑(4-氨基-N-(5-甲基异恶唑-3-基)-苯磺酰胺-SMX)的生物降解性。改性包括用大气代替过氧化氢并加入硫酸铜作为反应促进剂。进行了两个系列的实验。第一次(系列1)仅使用充气催化剂进行。在第二系列(系列2)中,使用了UVA辐射和曝气循环。在UVA辐射过程中,磺胺甲恶唑的去除速度不及仅在充气溶液中。在这两个过程中经过1.5小时后,SMX降解在系列2中为23%,在系列1中为59%。观察到相反的矿化趋势,系列2中的DOC去除比系列1高约5%。与磺胺甲恶唑溶液的提取物相比,四种极性不同的有机溶剂产生的反应产物的提取物的FTIR光谱显示,反应后混合物中的官能团差异很大。基于FTIR分析,提出了磺胺甲恶唑的几种氧化产物。显然,羟基自由基最初会攻击磺酰胺键,导致形成磺胺酸和3-氨基-5-甲基异恶唑。不管毒性试验中使用的参考生物如何,系列2中的反应后混合物比系列1中的反应后混合物更具毒性。相反,以BOD5 / DOC比计算的生物降解性对于反应后更高。混合物2的量为0.43。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号