Construction of a C-decorated and Cu-doped (Fe,Cu)S/CuFe 2 O 4 solid solution for photo-Fenton degradation of hydrophobic organic contaminant: Enhanced electron transfer and adsorption capacity
Chemosphere, ISSN: 0045-6535, Vol: 296, Page: 134005
2022
- 21Citations
- 17Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations21
- Citation Indexes21
- 21
- CrossRef15
- Captures17
- Readers17
- 17
Article Description
To effectively treat the hydrophobic organic contaminant and utilize an industrial solid waste manganese residue (MR), a novel starch-derived carbon (SC)-decorated and Cu-doped (Fe,Cu)S/CuFe 2 O 4 solid solution (CFS/CFO@SC) was prepared from MR via mechanical activation treatment of precursor materials followed by one-step pyrolysis and applied as a photo-Fenton catalyst to treat a hydrophobic organic compound, 17α-ethinylestradiol (EE2). Characterization results showed that the CFS/CFO@SC solid solution with unique crystal and electronic structures exhibited high adsorption capacity and catalytic activity, ascribed to that Cu doping and C decorating enhanced its hydrophobicity and BET surface area. The CFS/CFO@SC showed excellent degradation efficiency with nearly 100% of EE2 removal rate in 40 min (degradation rate constant of 0.112 min −1 ), and a high mineralization degree with 95.2% of TOC removal in 180 min. This could be ascribed to that C decorating and the formation of CFS/CFO solid solution promoted the charge transfer in a continuous band, resulting in effective separation of photogenerated holes–electrons (h + –e – ). The strong interaction of Fe–Cu collaborating with the photoelectron could effectively accelerate the recycle of Fe 3+ /Fe 2+ and Cu 2+ /Cu +, thus generating more active radicals. Moreover, CFS/CFO@SC showed promising stability and recyclability with the EE2 removal rates all >95% after five cycles. This work brings a valuable approach for the rational design of high-performance Fe-based photo-Fenton catalysts for environmental remediation and the valorization of MR.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0045653522004982; http://dx.doi.org/10.1016/j.chemosphere.2022.134005; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85124722091&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/35181432; https://linkinghub.elsevier.com/retrieve/pii/S0045653522004982; https://dx.doi.org/10.1016/j.chemosphere.2022.134005
Elsevier BV
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