期刊
JOURNAL OF WATER PROCESS ENGINEERING
卷 33, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.jwpe.2019.101010
关键词
Radical oxidation; Metal-organic frameworks; Emerging organic contaminants; Degradation; Light emitting diode
资金
- National Natural Science Foundation of China [51778270]
- Fundamental Research Funds for the Central Universities [21617448]
Metal-organic frameworks (MOFs) have become one of the most attractive classes of materials due to their versatile features. It is desirable to evaluate the photocatalysis performance of MOFs in aquatic medium. In this study, graphene oxide compositing MIL-101(Fe) (GO@MIL-101(Fe)) was fabricated. Based on this MOF, a light/MOF/H2O2 photocatalysis system was developed to degrade tris(2-chloroethyl) phosphate (TCEP). GO@MIL-101(Fe) has a lower band gap energy (2.17 eV) than MIL-101(Fe) (2.41 eV), suggesting an expansion of visible light absorption from 520 nm to 570 nm. Under 420 nm irradiation, removal of TCEP under the 15%GO@MIL-101(Fe) photocatalysis system followed pseudo-first-order kinetic with a reaction rate constant at 1.64 x 10(-3) s(-1). Using GO@MIL-101(Fe), a fast activation and electron transfer was achieved due to the high conductibility of GO, resulting in a higher removal efficiency of TCEP (similar to 95% at 30 min) than using MIL-101(Fe) (similar to 50%). The basic reaction mechanism involved the excitation of electrons from HOMO (oxygen orbitals in ligands) to LUMO (Fe(II)/Fe(III) in core nodes) induced by visible light irradiation, followed by the electron transport between GO@MIL-101(Fe) and H2O2 to generate (OH)-O-center dot. GO@MIL-101(Fe) visible-light photocatalysis would be a potential treatment process for organic contaminants.
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