{"title":"Effect of persulfate dosage on organic degradation using N-doped biochar: Reaction pathway and environmental implications.","authors":"Shijia Li, Ruonan Duan, Yandi Hu, Jingqi Wu, Tongshuai Wang, Wei Tang, Zhixiong Li, Wu Qin, Jiawei Chen","doi":"10.1002/wer.70054","DOIUrl":null,"url":null,"abstract":"<p><p>Persulfate-based advanced oxidation processes (PS-AOPs) catalyzed by carbon-based catalysts are promising for removing organic pollutants via radical/non-radical pathways. However, the activation efficiency of peroxymonosulfate (PMS) or peroxydisulfate (PDS) usage and the reaction mechanism remain insufficiently understood. In this study, the effects of PMS/PDS dosage on the degradation of bisphenol A (BPA, 10 mg/L) were evaluated using N-doped biochar (N-BC, 0.2 g/L) assisted PS-AOPs. The reaction pathways were comprehensively investigated through a combination of characterization techniques and molecular simulations. With low PS dosages (0.05 and 0.1 mM), the degradation rate constants ( <math> <semantics> <mrow><msub><mi>k</mi> <mi>obs</mi></msub> </mrow> <annotation>$$ {k}_{obs} $$</annotation></semantics> </math> ) were higher in N-BC/PDS (0.04 and 0.07 min<sup>-1</sup>) compared to N-BC/PMS (0.02 and 0.04 min<sup>-1</sup>), likely due to higher PDS utilization, which enhanced the contribution of the non-radical pathway. Interestingly, with higher PS dosages (0.5 and 1.5 mM), the <math> <semantics> <mrow><msub><mi>k</mi> <mi>obs</mi></msub> </mrow> <annotation>$$ {k}_{obs} $$</annotation></semantics> </math> values were 0.16 min<sup>-1</sup> and 0.18 min<sup>-1</sup> in N-BC/PMS, respectively, significantly exceeding those determined in N-BC/PDS (0.11 and 0.11 min<sup>-1</sup>). This result stemmed from the greater adsorption capacity of N-BC for PMS compared to PDS, leading to increased formation of <sup>1</sup>O<sub>2</sub>. The contribution of non-radical pathways for both PMS and PDS increased with higher PS dosage. The results highlighted that BPA degradation improved significantly with the increase in PMS dosage; meanwhile, BPA degradation was insensitive to PDS dosage. The optimal PMS dosage for BPA degradation was found to be 1.5 mM and 0.1 mM for PDS. This study offered valuable insights for optimizing PS-AOPs in environmental remediation, helping to guide the selection of appropriate oxidants and dosages for maximizing pollutant removal. PRACTITIONER POINTS: Effect of PMS/PDS dosage on BPA degradation by N-doped biochar was revealed. Contribution of dominated non-radical pathway increased as PMS/PDS dosage increased. The greater PDS utilization and non-radical pathway resulted in the higher <math> <semantics> <mrow><msub><mi>k</mi> <mi>obs</mi></msub> </mrow> <annotation>$$ {k}_{obs} $$</annotation></semantics> </math> at low dosage. N-BC adsorbed more PMS than PDS, leading to an increase in <math> <semantics> <mrow><msub><mi>k</mi> <mi>obs</mi></msub> </mrow> <annotation>$$ {k}_{obs} $$</annotation></semantics> </math> at high dosage.</p>","PeriodicalId":23621,"journal":{"name":"Water Environment Research","volume":"97 3","pages":"e70054"},"PeriodicalIF":2.5000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Water Environment Research","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1002/wer.70054","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}
引用次数: 0
Abstract
Persulfate-based advanced oxidation processes (PS-AOPs) catalyzed by carbon-based catalysts are promising for removing organic pollutants via radical/non-radical pathways. However, the activation efficiency of peroxymonosulfate (PMS) or peroxydisulfate (PDS) usage and the reaction mechanism remain insufficiently understood. In this study, the effects of PMS/PDS dosage on the degradation of bisphenol A (BPA, 10 mg/L) were evaluated using N-doped biochar (N-BC, 0.2 g/L) assisted PS-AOPs. The reaction pathways were comprehensively investigated through a combination of characterization techniques and molecular simulations. With low PS dosages (0.05 and 0.1 mM), the degradation rate constants ( ) were higher in N-BC/PDS (0.04 and 0.07 min-1) compared to N-BC/PMS (0.02 and 0.04 min-1), likely due to higher PDS utilization, which enhanced the contribution of the non-radical pathway. Interestingly, with higher PS dosages (0.5 and 1.5 mM), the values were 0.16 min-1 and 0.18 min-1 in N-BC/PMS, respectively, significantly exceeding those determined in N-BC/PDS (0.11 and 0.11 min-1). This result stemmed from the greater adsorption capacity of N-BC for PMS compared to PDS, leading to increased formation of 1O2. The contribution of non-radical pathways for both PMS and PDS increased with higher PS dosage. The results highlighted that BPA degradation improved significantly with the increase in PMS dosage; meanwhile, BPA degradation was insensitive to PDS dosage. The optimal PMS dosage for BPA degradation was found to be 1.5 mM and 0.1 mM for PDS. This study offered valuable insights for optimizing PS-AOPs in environmental remediation, helping to guide the selection of appropriate oxidants and dosages for maximizing pollutant removal. PRACTITIONER POINTS: Effect of PMS/PDS dosage on BPA degradation by N-doped biochar was revealed. Contribution of dominated non-radical pathway increased as PMS/PDS dosage increased. The greater PDS utilization and non-radical pathway resulted in the higher at low dosage. N-BC adsorbed more PMS than PDS, leading to an increase in at high dosage.
期刊介绍:
Published since 1928, Water Environment Research (WER) is an international multidisciplinary water resource management journal for the dissemination of fundamental and applied research in all scientific and technical areas related to water quality and resource recovery. WER''s goal is to foster communication and interdisciplinary research between water sciences and related fields such as environmental toxicology, agriculture, public and occupational health, microbiology, and ecology. In addition to original research articles, short communications, case studies, reviews, and perspectives are encouraged.