研究报告

  • 杨博文,张环,李爽爽.聚合多巴胺功能化非织造布增强Fe2+活化过硫酸盐降解酸性红B[J].环境科学学报,2022,42(7):209-216

  • 聚合多巴胺功能化非织造布增强Fe2+活化过硫酸盐降解酸性红B
  • Enhanced degradation of acid red B by Fe2+ activated persulfate with polydopamine functionalized nonwovens cloth
  • 基金项目:国家自然科学基金资助(No. 52070142); 天津市高等学校创新团队培养计划(No. TD13-5042)
  • 作者
  • 单位
  • 杨博文
  • 天津工业大学环境科学与工程学院,天津 300387;天津工业大学省部共建分离膜与膜过程国家重点实验室,天津 300387
  • 张环
  • 天津工业大学环境科学与工程学院,天津 300387;天津工业大学省部共建分离膜与膜过程国家重点实验室,天津 300387
  • 李爽爽
  • 天津工业大学环境科学与工程学院,天津 300387;天津工业大学省部共建分离膜与膜过程国家重点实验室,天津 300387
  • 摘要:为了提高Fe2+活化过硫酸盐(PS)过程中Fe2+的利用效率,降低其对自由基的淬灭作用.制备了聚多巴胺复合聚丙烯非织造布(PDA-PP),考察了PDA-PP材料应用于Fe2+/PS体系中,对酸性红B(ARB)的氧化降解性能和机理.结果表明:PDA-PP/Fe2+/PS体系能够更持续地活化PS氧化降解ARB.一方面聚多巴胺中酚羟基使Fe3+还原为Fe2+,保持对PS分解的持续性,另一方面聚多巴胺中的邻苯二酚和氨基对Fe2+的络合作用控制了Fe2+的释放速率,降低了Fe2+对自由基的淬灭.自由基淬灭实验与ESR分析结果表明,羟基自由基(·OH)是PDA-PP/Fe2+/PS体系的主要活性物种. (SO4·-)的产生量少于·OH.研究显示,PDA-PP的加入能有效提高Fe2+/PS体系中Fe2+ 的利用效率,降低自由基的淬灭作用,PDA-PP在重复使用5次后,催化体系依然保持催化性能.该研究在促进过硫酸盐催化氧化降解有机物方向具有一定的应用潜力.
  • Abstract:In this study, polydopamine composite polypropylene nonwovens (PDA-PP) were prepared and utilized in the process of Fe2+ activated persulfate (PS) to enhance the activation efficiency and reduce the quenching effect of Fe2+ on free radicals. The performance and mechanism of acid red B (ARB) degradation by PDA-PP/Fe2+/PS were investigated. The results indicated that PS could continuously be activated by PDA-PP/Fe2+ for ARB catalytic degradation. The Fe3+ could be reduced to Fe2+ by phenolic hydroxyl group in polydopamine and active PS continuously. The complexation of catechol and amino group in polydopamine with Fe2+ could control the release of Fe2+ and reduce the quenching of free radicals. The results of radical quenching experiments and ESR analysis showed that hydroxyl radical (·OH) is the main active species in PDA-PP/Fe2+/PS system. The yield of SO4·- is lower than ·OH. After the reuse of PDA-PP for 5 times, the PDA-PP/Fe2+/PS still maintains the catalytic performance. This study has a certain application potential on developing persulfate catalytic oxidation for organic compounds.

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