{"title":"单宁酸和 g-C3N4 自组装成掺氮分层多孔碳以增强 PMS 活性","authors":"Jiamei Qian, Fengzhen Wu, Yunjiao Jiang, Zhirui Zuo, Lirong Tang, Guanfeng Lin, Biao Huang, Beili Lu","doi":"10.1016/j.jwpe.2024.106616","DOIUrl":null,"url":null,"abstract":"<div><div>The emerging field of persulfate-based advanced oxidation focused on heteroatom-doped carbon catalysts for their tunable catalytic properties and environmental benefits. Here, a novel nitrogen-doped porous carbon catalyst (N-C-T) was synthesized by self-assembling tannic acid with g-C<sub>3</sub>N<sub>4</sub> nanosheets, followed by carbonization. The g-C₃N₄ nanosheets played a critical role in forming a nitrogen-rich hierarchical porous structure, significantly boosting PMS activation and enhancing phenol degradation efficiency. The optimized catalyst, N-C-900, showed superior performance, removing 97.6 % of phenol in 30 min with a rate constant of 0.121 min<sup>−1</sup>, 30 times higher than tannic acid-derived TA-900 catalyst. Surface-bound radicals were identified as the primary reactive species in the N-C-900/PMS system. The enhanced adsorption of PMS and phenol on the surface of N-C-900 was conducive to the generation of surface-bound radicals, thereby accelerating phenol degradation. Furthermore, the N-C-900/PMS system also exhibited good reusability and stability across a pH range of 3.5 to 9.5. This study provides insights into designing nitrogen-doped hierarchical porous carbon catalysts and sheds light on the possible catalytic mechanisms during PMS activation.</div></div>","PeriodicalId":17528,"journal":{"name":"Journal of water process engineering","volume":"69 ","pages":"Article 106616"},"PeriodicalIF":6.3000,"publicationDate":"2024-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-assembly of tannic acid and g-C3N4 into nitrogen-doped hierarchical porous carbon for enhanced PMS activation\",\"authors\":\"Jiamei Qian, Fengzhen Wu, Yunjiao Jiang, Zhirui Zuo, Lirong Tang, Guanfeng Lin, Biao Huang, Beili Lu\",\"doi\":\"10.1016/j.jwpe.2024.106616\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The emerging field of persulfate-based advanced oxidation focused on heteroatom-doped carbon catalysts for their tunable catalytic properties and environmental benefits. Here, a novel nitrogen-doped porous carbon catalyst (N-C-T) was synthesized by self-assembling tannic acid with g-C<sub>3</sub>N<sub>4</sub> nanosheets, followed by carbonization. The g-C₃N₄ nanosheets played a critical role in forming a nitrogen-rich hierarchical porous structure, significantly boosting PMS activation and enhancing phenol degradation efficiency. The optimized catalyst, N-C-900, showed superior performance, removing 97.6 % of phenol in 30 min with a rate constant of 0.121 min<sup>−1</sup>, 30 times higher than tannic acid-derived TA-900 catalyst. Surface-bound radicals were identified as the primary reactive species in the N-C-900/PMS system. The enhanced adsorption of PMS and phenol on the surface of N-C-900 was conducive to the generation of surface-bound radicals, thereby accelerating phenol degradation. Furthermore, the N-C-900/PMS system also exhibited good reusability and stability across a pH range of 3.5 to 9.5. This study provides insights into designing nitrogen-doped hierarchical porous carbon catalysts and sheds light on the possible catalytic mechanisms during PMS activation.</div></div>\",\"PeriodicalId\":17528,\"journal\":{\"name\":\"Journal of water process engineering\",\"volume\":\"69 \",\"pages\":\"Article 106616\"},\"PeriodicalIF\":6.3000,\"publicationDate\":\"2024-11-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of water process engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2214714424018488\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of water process engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214714424018488","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
Self-assembly of tannic acid and g-C3N4 into nitrogen-doped hierarchical porous carbon for enhanced PMS activation
The emerging field of persulfate-based advanced oxidation focused on heteroatom-doped carbon catalysts for their tunable catalytic properties and environmental benefits. Here, a novel nitrogen-doped porous carbon catalyst (N-C-T) was synthesized by self-assembling tannic acid with g-C3N4 nanosheets, followed by carbonization. The g-C₃N₄ nanosheets played a critical role in forming a nitrogen-rich hierarchical porous structure, significantly boosting PMS activation and enhancing phenol degradation efficiency. The optimized catalyst, N-C-900, showed superior performance, removing 97.6 % of phenol in 30 min with a rate constant of 0.121 min−1, 30 times higher than tannic acid-derived TA-900 catalyst. Surface-bound radicals were identified as the primary reactive species in the N-C-900/PMS system. The enhanced adsorption of PMS and phenol on the surface of N-C-900 was conducive to the generation of surface-bound radicals, thereby accelerating phenol degradation. Furthermore, the N-C-900/PMS system also exhibited good reusability and stability across a pH range of 3.5 to 9.5. This study provides insights into designing nitrogen-doped hierarchical porous carbon catalysts and sheds light on the possible catalytic mechanisms during PMS activation.
期刊介绍:
The Journal of Water Process Engineering aims to publish refereed, high-quality research papers with significant novelty and impact in all areas of the engineering of water and wastewater processing . Papers on advanced and novel treatment processes and technologies are particularly welcome. The Journal considers papers in areas such as nanotechnology and biotechnology applications in water, novel oxidation and separation processes, membrane processes (except those for desalination) , catalytic processes for the removal of water contaminants, sustainable processes, water reuse and recycling, water use and wastewater minimization, integrated/hybrid technology, process modeling of water treatment and novel treatment processes. Submissions on the subject of adsorbents, including standard measurements of adsorption kinetics and equilibrium will only be considered if there is a genuine case for novelty and contribution, for example highly novel, sustainable adsorbents and their use: papers on activated carbon-type materials derived from natural matter, or surfactant-modified clays and related minerals, would not fulfil this criterion. The Journal particularly welcomes contributions involving environmentally, economically and socially sustainable technology for water treatment, including those which are energy-efficient, with minimal or no chemical consumption, and capable of water recycling and reuse that minimizes the direct disposal of wastewater to the aquatic environment. Papers that describe novel ideas for solving issues related to water quality and availability are also welcome, as are those that show the transfer of techniques from other disciplines. The Journal will consider papers dealing with processes for various water matrices including drinking water (except desalination), domestic, urban and industrial wastewaters, in addition to their residues. It is expected that the journal will be of particular relevance to chemical and process engineers working in the field. The Journal welcomes Full Text papers, Short Communications, State-of-the-Art Reviews and Letters to Editors and Case Studies