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Activation of periodate by biocarbon-supported multiple modified nanoscale iron for the degradation of bisphenol A in high-temperature aqueous solution.
Zhao, Jingnan; Chen, Junwen; Wang, Qun; Xiong, Renxuan; Ma, Jun.
Afiliação
  • Zhao J; The IT Electronics Eleventh Design & Research Institute Scientific and Technological Engineering Co., LTD, Chengdu, 610021, People's Republic of China.
  • Chen J; Faculty of Geoscience and Environmental Engineering, Southwest Jiaotong University, Chengdu, 610031, People's Republic of China.
  • Wang Q; Faculty of Geoscience and Environmental Engineering, Southwest Jiaotong University, Chengdu, 610031, People's Republic of China.
  • Xiong R; School of Chemical Engineering, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Ma J; Faculty of Geoscience and Environmental Engineering, Southwest Jiaotong University, Chengdu, 610031, People's Republic of China. xhlu_swjtu@126.com.
Environ Sci Pollut Res Int ; 31(16): 24263-24281, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38436863
ABSTRACT
As reported, the persistent toxic and harmful pollutant bisphenol A (BPA) from industrial emissions has been consistently found in aquatic environments inhabited by humans. Periodate (PI)-based advanced oxidation processes (AOPs) have been employed to degrade BPA, although activating PI proves more challenging compared to other oxidants. A novel nano iron metal catalyst, sulfided nanoscale iron-nickel bimetallic nanoparticle supported on biocarbon (S-(nFe0-Ni)/BC) was synthesized and utilized to activate PI for the removal of BPA. The morphology, structure, and composition of S-(nFe0-Ni)/BC were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy-energy dispersive spectrometer (SEM-EDS), and fourier-transform infrared spectrum (FTIR). The catalyst demonstrates an excellent ability to activate PI, achieving a BPA removal efficacy of 86.4%, accompanied by a 33% reduction in total organic carbon (TOC) in the {S-(nFe0-Ni)/BC}/PI system. BPA degradation exhibited a significant change at the 5-min mark. In the first stage (0-5 min), nonlinear dynamic fitting research, combined with scavenging experiments, unveiled the competitive degradation of pollutants primarily driven by iodate radical ( IO 3 · ), singlet oxygen 1 O 2 , and hydroxyl radical ( · OH ). The competitive dynamics aligned with the ExpAssoc model. The contribution rates of different active species during the second stage (5-120 min) were calculated. The contributions of main species to BPA removal follow the order of IO 3 · > 1 O 2 > · OH throughout the entire process. The influence of various parameters, such as the dosage of S-(nFe0-Ni)/BC, initial PI concentration, BPA concentration, pH, temperature, and the presence of coexisting anions, was also examined. Finally, a plausible reaction mechanism in the system is proposed, suggesting that the {S-(nFe0-Ni)/BC}/PI system involves a heterogeneous synergistic reaction occurring primarily on the surface of S-(nFe0-Ni)/BC. Therefore, this study proposes a promising approach for PI-based AOPs to degrade organic pollutants, aiming to mitigate the irreversible harm caused by such pollutants to organisms and the environment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenóis / Poluentes Químicos da Água / Compostos Benzidrílicos / Ácido Periódico / Ferro Limite: Humans Idioma: En Revista: Environ Sci Pollut Res Int Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenóis / Poluentes Químicos da Água / Compostos Benzidrílicos / Ácido Periódico / Ferro Limite: Humans Idioma: En Revista: Environ Sci Pollut Res Int Ano de publicação: 2024 Tipo de documento: Article