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Multifunctional capacity of CoMnFe-LDH/LDO activated peroxymonosulfate for p-arsanilic acid removal and inorganic arsenic immobilization: Performance and surface-bound radical mechanism.
Ye, Cheng; Deng, Jing; Huai, Lingyi; Cai, Anhong; Ling, Xiao; Guo, Hongguang; Wang, Qiongfang; Li, Xueyan.
Afiliação
  • Ye C; College of Civil Engineering, Zhejiang University of Technology, Hangzhou 310023, China.
  • Deng J; College of Civil Engineering, Zhejiang University of Technology, Hangzhou 310023, China. Electronic address: zjut_djing@163.com.
  • Huai L; College of Civil Engineering, Zhejiang University of Technology, Hangzhou 310023, China.
  • Cai A; College of Civil Engineering, Zhejiang University of Technology, Hangzhou 310023, China.
  • Ling X; College of Civil Engineering, Zhejiang University of Technology, Hangzhou 310023, China.
  • Guo H; MOE Key Laboratory of Deep Earth Science and Engineering, College of Architecture and Environment, Sichuan University, Chengdu 610065, China.
  • Wang Q; College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai 201600, China.
  • Li X; School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China.
Sci Total Environ ; 806(Pt 1): 150379, 2022 Feb 01.
Article em En | MEDLINE | ID: mdl-34571222
ABSTRACT
Organoarsenic contaminants existing in water body threat human health and ecological environment due to insufficient bifunctional treatment technologies for organoarsenic degradation and inorganic arsenic immobilization. In order to safely and efficiently treat organoarsenic contaminants discharged into the aquatic environment, Co-Mn-Fe layered double hydroxide (CoMnFe-LDH) and Co-Mn-Fe layered double oxide (CoMnFe-LDO) were fabricated and employed as peroxymonosulfate (PMS) activator for organoarsenic degradation and inorganic arsenic immobilization, and p-arsanilic acid (p-ASA) was selected as target pollutant. Results demonstrated that the satisfactory removal of p-ASA (100.0%) in both CoMnFe-LDH/PMS and CoMnFe-LDO/PMS systems was obtained within 30 min, and substantial inorganic arsenic adsorption could be achieved (below 0.5 mg/L) in two systems with converting major inorganic arsenic species to arsenate. As XPS, ESR and quenching experiment revealed, the existence and generation of surface-bound radicals in two systems were identified. Based on density functional theory calculation and XPS analysis, the catalytic mechanism of CoMnFe-LDO/PMS system that PMS could be activated via direct electron transfer from adsorbed p-ASA was clarified, which differed from PMS activation via coupling with surface hydroxyl groups in CoMnFe-LDH/PMS system. Catalytic performance assessment under various critical operation parameters indicated that CoMnFe-LDH presented more stable ability of p-ASA removal in a wide pH range and complex aquatic environment. The recycle experiment demonstrated the excellent stability and reusability of CoMnFe-LDH(LDO). Besides, seven degradation products of p-ASA in CoMnFe-LDH/PMS system including phenolic compounds, azophenylarsonic acid, nitrobenzene and benzoquinne were identified by UV-Vis spectra and LC-TOF-MS analysis, and the corresponding degradation pathway was proposed. In summary, compared to CoMnFe-LDO/PMS, CoMnFe-LDH/PMS holds great promise for the development of an oxidation-adsorption process for efficient control of organoarsenic pollutant.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácido Arsanílico / Arsênio Limite: Humans Idioma: En Revista: Sci Total Environ Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácido Arsanílico / Arsênio Limite: Humans Idioma: En Revista: Sci Total Environ Ano de publicação: 2022 Tipo de documento: Article