Valorization of plastics and goethite into iron-carbon composite as persulfate activator for amaranth oxidation

Valorization of plastics and goethite into iron-carbon composite as persulfate activator for amaranth oxidation
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DOI:
10.1016/j.cej.2020.127188
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发表时间:
2020-10
影响因子:
15.1
通讯作者:
Gihoon Kwon;Dong-wan Cho;Kwangsuk Yoon;Hocheol Song
Gihoon Kwon;Dong-wan Cho;Kwangsuk Yoon;Hocheol Song
中科院分区:
工程技术1区
文献类型:
--
作者:
Gihoon Kwon;Dong-wan Cho;Kwangsuk Yoon;Hocheol Song

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In this work, iron-carbon composites were prepared by co-pyrolysis of polyethylene (PE) and goethite (α-FeO(OH)) and used as a persulfate (S2O82−) activator for catalytic oxidation of an azo dye chemical, amaranth. The instrumental characterization of the composites indicated the composites were composed of graphitic carbon layers embedded with iron minerals. The graphitic property of the carbon and the types of iron mineral phase in the composites were highly dependent on the pyrolytic temperature employed during their production. The increase of pyrolytic temperature led to more graphitization of carbon as well as sequential phase transformation of goethite into hematite (α-Fe2O3) at 250 °C, magnetite (Fe3O4) at 600 °C, and wustite (FeO)/zero-valent iron (Fe0) at 900 °C. Amaranth degradation experiments with the composite produced from PE:goethite mixture at 2:1 mass ratio at 900 °C resulted in complete removal of 10 mg L−1amaranth within 5 min in the presence of 0.1 g L−1composite and 4 mM persulfate. Oxidation of amaranth occurred through reactions with hydroxyl- (OHradical dot) and sulfate radicals (SO4radical dot−) generated from S2O82activation by the composite, and experiments with quenching agents suggested SO4radical dot−was more dominant radical in the oxidation process. The catalytic ability of the composite for S2O82−activation was well maintained during 10 repeated cycles of amaranth degradation. As a result, it was demonstrated that iron-loaded S2O82−activator can be prepared through a strategic combination of iron oxide and plastic by using co-pyrolysis.