{"title":"Fe3+和H2O2辅助多巴胺在三聚氰胺泡沫上快速聚合以激活PMS降解有机污染物†","authors":"Haoxiang Yan, Jianzheng Zhen and Yuyuan Yao","doi":"10.1039/D4EW00596A","DOIUrl":null,"url":null,"abstract":"<p >Developing a facile preparation method to construct separable and recyclable Fenton-like catalysts holds great significance in the field of environmental remediation. Herein, a rapid dopamine (DA) polymerization strategy to modify melamine foam (MF) was proposed for the construction of bulk foam catalytic materials, which was further utilized for peroxymonosulfate (PMS) activation to degrade organic pollutants. Taking advantage of the chelation between dopamine's catechol group and Fe<small><sup>3+</sup></small>, as well as the oxidative environment provided by H<small><sub>2</sub></small>O<small><sub>2</sub></small>, DA could encapsulate and polymerize on the surface of MF within 2 h to obtain the MF@Fe@PDA catalyst. Detailed experimental results demonstrated that MF@Fe@PDA could efficiently activate PMS to achieve almost 100% removal of bisphenol A (BPA) in 20 min, and the corresponding turnover frequency (TOF) value was one order of magnitude higher than that of the homogeneous (Fe<small><sup>2+</sup></small>, Fe<small><sup>3+</sup></small>) and nanoparticle (Fe<small><sup>0</sup></small>) catalysts. The high activity of the MF@Fe@PDA/PMS system stemmed from the Fe sites and carbonyl group (C<img>O), which could induce the activation of PMS for the rapid generation of singlet oxygen (<small><sup>1</sup></small>O<small><sub>2</sub></small>), sulfate radical (SO<small><sub>4</sub></small>˙<small><sup>−</sup></small>) and hydroxyl radicals (˙OH). Meanwhile, the coexisting bicarbonate ions (HCO<small><sub>3</sub></small><small><sup>−</sup></small>) in the MF@Fe@PDA/PMS system could enhance the generation of <small><sup>1</sup></small>O<small><sub>2</sub></small>, thereby accelerating the degradation of BPA. Moreover, a flow-through system assisted by the bulk MF@Fe@PDA catalyst was constructed for organic pollutant degradation. Overall, these findings may open up new possibilities for developing highly efficient catalysts for wastewater remediation.</p>","PeriodicalId":75,"journal":{"name":"Environmental Science: Water Research & Technology","volume":" 11","pages":" 2698-2708"},"PeriodicalIF":3.5000,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fe3+ and H2O2 assisted dopamine rapid polymerization on melamine foam to activate PMS for organic pollutant degradation†\",\"authors\":\"Haoxiang Yan, Jianzheng Zhen and Yuyuan Yao\",\"doi\":\"10.1039/D4EW00596A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Developing a facile preparation method to construct separable and recyclable Fenton-like catalysts holds great significance in the field of environmental remediation. Herein, a rapid dopamine (DA) polymerization strategy to modify melamine foam (MF) was proposed for the construction of bulk foam catalytic materials, which was further utilized for peroxymonosulfate (PMS) activation to degrade organic pollutants. Taking advantage of the chelation between dopamine's catechol group and Fe<small><sup>3+</sup></small>, as well as the oxidative environment provided by H<small><sub>2</sub></small>O<small><sub>2</sub></small>, DA could encapsulate and polymerize on the surface of MF within 2 h to obtain the MF@Fe@PDA catalyst. Detailed experimental results demonstrated that MF@Fe@PDA could efficiently activate PMS to achieve almost 100% removal of bisphenol A (BPA) in 20 min, and the corresponding turnover frequency (TOF) value was one order of magnitude higher than that of the homogeneous (Fe<small><sup>2+</sup></small>, Fe<small><sup>3+</sup></small>) and nanoparticle (Fe<small><sup>0</sup></small>) catalysts. The high activity of the MF@Fe@PDA/PMS system stemmed from the Fe sites and carbonyl group (C<img>O), which could induce the activation of PMS for the rapid generation of singlet oxygen (<small><sup>1</sup></small>O<small><sub>2</sub></small>), sulfate radical (SO<small><sub>4</sub></small>˙<small><sup>−</sup></small>) and hydroxyl radicals (˙OH). Meanwhile, the coexisting bicarbonate ions (HCO<small><sub>3</sub></small><small><sup>−</sup></small>) in the MF@Fe@PDA/PMS system could enhance the generation of <small><sup>1</sup></small>O<small><sub>2</sub></small>, thereby accelerating the degradation of BPA. Moreover, a flow-through system assisted by the bulk MF@Fe@PDA catalyst was constructed for organic pollutant degradation. Overall, these findings may open up new possibilities for developing highly efficient catalysts for wastewater remediation.</p>\",\"PeriodicalId\":75,\"journal\":{\"name\":\"Environmental Science: Water Research & Technology\",\"volume\":\" 11\",\"pages\":\" 2698-2708\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental Science: Water Research & Technology\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ew/d4ew00596a\",\"RegionNum\":4,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENGINEERING, ENVIRONMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science: Water Research & Technology","FirstCategoryId":"93","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ew/d4ew00596a","RegionNum":4,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
Fe3+ and H2O2 assisted dopamine rapid polymerization on melamine foam to activate PMS for organic pollutant degradation†
Developing a facile preparation method to construct separable and recyclable Fenton-like catalysts holds great significance in the field of environmental remediation. Herein, a rapid dopamine (DA) polymerization strategy to modify melamine foam (MF) was proposed for the construction of bulk foam catalytic materials, which was further utilized for peroxymonosulfate (PMS) activation to degrade organic pollutants. Taking advantage of the chelation between dopamine's catechol group and Fe3+, as well as the oxidative environment provided by H2O2, DA could encapsulate and polymerize on the surface of MF within 2 h to obtain the MF@Fe@PDA catalyst. Detailed experimental results demonstrated that MF@Fe@PDA could efficiently activate PMS to achieve almost 100% removal of bisphenol A (BPA) in 20 min, and the corresponding turnover frequency (TOF) value was one order of magnitude higher than that of the homogeneous (Fe2+, Fe3+) and nanoparticle (Fe0) catalysts. The high activity of the MF@Fe@PDA/PMS system stemmed from the Fe sites and carbonyl group (CO), which could induce the activation of PMS for the rapid generation of singlet oxygen (1O2), sulfate radical (SO4˙−) and hydroxyl radicals (˙OH). Meanwhile, the coexisting bicarbonate ions (HCO3−) in the MF@Fe@PDA/PMS system could enhance the generation of 1O2, thereby accelerating the degradation of BPA. Moreover, a flow-through system assisted by the bulk MF@Fe@PDA catalyst was constructed for organic pollutant degradation. Overall, these findings may open up new possibilities for developing highly efficient catalysts for wastewater remediation.
期刊介绍:
Environmental Science: Water Research & Technology seeks to showcase high quality research about fundamental science, innovative technologies, and management practices that promote sustainable water.