Pengyi Wang , Fan Kang , Xiangbin Huang , Zhipeng Luo , Jing Zou , Min Yang , Meng Sun , Xin Yu , Huabin Zeng
{"title":"Fenton过程中羟基自由基对ph值的响应","authors":"Pengyi Wang , Fan Kang , Xiangbin Huang , Zhipeng Luo , Jing Zou , Min Yang , Meng Sun , Xin Yu , Huabin Zeng","doi":"10.1016/j.ese.2025.100566","DOIUrl":null,"url":null,"abstract":"<div><div>Efficient management of temporal latency and spatial heterogeneity remains a critical challenge in sensor-based pH regulation for smart water management, primarily due to inherent response delays and mass transfer constraints. In oxidation systems with dynamic pH environments, delayed responses can lead to issues such as cyanide release, unwanted side reactions, or pipe damage. To address these challenges, we propose a “pause-then-adjust” control strategy, exploiting the pH-responsive generation of hydroxyl radicals (<sup>•</sup>OH) in a modified Fenton reaction system. This system utilizes hydroxylamine as an electron donor and ethylenediaminetetraacetic acid (EDTA) as a stabilizer for iron ions. Within the pH range of 7.0–10.0, the coexistence of [Fe<sup>2+</sup>-EDTA]<sup>2−</sup> and [Fe<sup>3+</sup>-OH-EDTA]<sup>2−</sup> complexes facilitates efficient electron transfer, resulting in the selective and sustained production of <sup>•</sup>OH radicals. The inherent pH-responsiveness of this strategy enables rapid and spatially coherent adjustments, offering a robust supplementary method for addressing complex and evolving requirements in advanced water treatment systems.</div></div>","PeriodicalId":34434,"journal":{"name":"Environmental Science and Ecotechnology","volume":"25 ","pages":"Article 100566"},"PeriodicalIF":14.0000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A pH-responsive production of hydroxyl radical in Fenton process\",\"authors\":\"Pengyi Wang , Fan Kang , Xiangbin Huang , Zhipeng Luo , Jing Zou , Min Yang , Meng Sun , Xin Yu , Huabin Zeng\",\"doi\":\"10.1016/j.ese.2025.100566\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Efficient management of temporal latency and spatial heterogeneity remains a critical challenge in sensor-based pH regulation for smart water management, primarily due to inherent response delays and mass transfer constraints. In oxidation systems with dynamic pH environments, delayed responses can lead to issues such as cyanide release, unwanted side reactions, or pipe damage. To address these challenges, we propose a “pause-then-adjust” control strategy, exploiting the pH-responsive generation of hydroxyl radicals (<sup>•</sup>OH) in a modified Fenton reaction system. This system utilizes hydroxylamine as an electron donor and ethylenediaminetetraacetic acid (EDTA) as a stabilizer for iron ions. Within the pH range of 7.0–10.0, the coexistence of [Fe<sup>2+</sup>-EDTA]<sup>2−</sup> and [Fe<sup>3+</sup>-OH-EDTA]<sup>2−</sup> complexes facilitates efficient electron transfer, resulting in the selective and sustained production of <sup>•</sup>OH radicals. The inherent pH-responsiveness of this strategy enables rapid and spatially coherent adjustments, offering a robust supplementary method for addressing complex and evolving requirements in advanced water treatment systems.</div></div>\",\"PeriodicalId\":34434,\"journal\":{\"name\":\"Environmental Science and Ecotechnology\",\"volume\":\"25 \",\"pages\":\"Article 100566\"},\"PeriodicalIF\":14.0000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental Science and Ecotechnology\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666498425000444\",\"RegionNum\":1,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science and Ecotechnology","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666498425000444","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
A pH-responsive production of hydroxyl radical in Fenton process
Efficient management of temporal latency and spatial heterogeneity remains a critical challenge in sensor-based pH regulation for smart water management, primarily due to inherent response delays and mass transfer constraints. In oxidation systems with dynamic pH environments, delayed responses can lead to issues such as cyanide release, unwanted side reactions, or pipe damage. To address these challenges, we propose a “pause-then-adjust” control strategy, exploiting the pH-responsive generation of hydroxyl radicals (•OH) in a modified Fenton reaction system. This system utilizes hydroxylamine as an electron donor and ethylenediaminetetraacetic acid (EDTA) as a stabilizer for iron ions. Within the pH range of 7.0–10.0, the coexistence of [Fe2+-EDTA]2− and [Fe3+-OH-EDTA]2− complexes facilitates efficient electron transfer, resulting in the selective and sustained production of •OH radicals. The inherent pH-responsiveness of this strategy enables rapid and spatially coherent adjustments, offering a robust supplementary method for addressing complex and evolving requirements in advanced water treatment systems.
期刊介绍:
Environmental Science & Ecotechnology (ESE) is an international, open-access journal publishing original research in environmental science, engineering, ecotechnology, and related fields. Authors publishing in ESE can immediately, permanently, and freely share their work. They have license options and retain copyright. Published by Elsevier, ESE is co-organized by the Chinese Society for Environmental Sciences, Harbin Institute of Technology, and the Chinese Research Academy of Environmental Sciences, under the supervision of the China Association for Science and Technology.