Enhancement of peroxydisulfate activation by inherent nature of Fe-N-P/C biochar derived from Capsosiphon fulvescens as a green biomass material for organic pollutants degradation

被引:14
作者
Seo, Giung [1 ]
Annamalai, Sivasankar [1 ,2 ]
Shin, Won Sik [1 ]
机构
[1] Kyungpook Natl Univ, Sch Architecture Civil Environm & Energy Engn, Daegu 41566, South Korea
[2] Saveetha Inst Med & Tech Sci, Saveetha Med Coll & Hosp, Ctr Global Hlth Res, Chennai 600077, India
关键词
Sulfadiazine; Seaweed biomass; Biochar; Peroxydisulfate; Superoxide; Electron transfer pathway; DOPED GRAPHENE; BISPHENOL-A; CARBON; REMOVAL; IRON; ANTIBIOTICS; OXIDATION; NITROGEN; BORON; NANOPARTICLES;
D O I
10.1016/j.cej.2023.146445
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study explores the catalytic activity of biochar materials derived from seaweed biomass (Capsosiphon fulvescens) for groundwater treatment. A facile pyrolysis process was utilized to prepare C. fulvescens biochar (CFBCX), where X represents the pyrolysis temperature. The instrumental analysis using surface characterization techniques revealed that CFBC800 inherently contained heteroatoms (N, P) and a trace metal (Fe) in the biochar. The adsorption kinetics and isotherm experiments depicted a mixed mechanism of physical and chemical adsorption of SDZ on CFBC. Consequently, in optimal conditions with 2 mM peroxydisulfate (PDS), 200 mg L-1 CFBC800, and 6.1 initial solution pH, SDZ degradation (>97.2%) is achieved within 60 min. Chemical quenching tests indicate the involvement of radical (O-2(center dot-) = 41.6%) and non-radical processes, including electron transfer (58.4%), in the PDS/CFBC800 system. The electron spin resonance spectroscopy confirmed the formation of reactive oxygen species (ROS) in the PDS/CFBC800 system, including radical (O-2(center dot-), SO4 center dot-, and HO center dot) and non-radical (O-1(2)) species. Furthermore, electrochemical studies demonstrated the existence of an electron transfer pathway in the non-radical process of the PDS/CFBC800 system. Based on chemical scavenger and ESR analyses, the PDS/CFBC800 system exhibited both radical and non-radical mechanisms, with the electron transfer pathway being more dominant in this catalytic system. The excellent catalytic activity of the PDS/CFBC800 system toward co-existing ions and various organic contaminant degradation is demonstrated. Moreover, the CFBC800-activated PDS system successfully demonstrated catalyst reusability in SDZ degradation. Thus, this study establishes CFBC800 as an ecofriendly catalyst with remarkable catalytic activity for groundwater remediation.
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页数:16
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