Iron oxide nanoparticles;
Silica microspheres;
Magnetic nanocomposites;
Fenton catalyst;
Water-treatment;
IRON-OXIDE;
DEGRADATION;
OXIDATION;
MANGANESE;
SILICAS;
ORANGE;
ROUTE;
D O I:
10.1016/j.apcatb.2013.01.046
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Maghemite nanoparticles (gamma-Fe2O3 NP) and maghemite/silica nanocomposite microspheres (gamma-Fe2O3/SiO2 MS) have been evaluated as magnetic heterogeneous Fenton catalysts. The catalysts were fully characterized by electronic microscopies, magnetometry, XRD, UV-vis-NIR spectroscopy, and sorption volumetry. It was found that the two materials differ in size, morphology, porosity and microstructure, although the maghemite nanoparticles are not modified by their encapsulation into the silica. Both catalysts have a strong magnetic susceptibility, but only the MS catalyst can be easily recovered by magnetic settlement. The mineralization and decolorization of aqueous solutions containing a model pollutant in presence of the catalysts were comparatively studied. Three model pollutants differing in their structure and their electrostatic charge were tested. The obtained reaction rates depend on the nature of the pollutant and catalyst The results indicate the existence of a correlation between the amount of adsorbed pollutant and the decolorization rate. The free NP are usually more active than the MS catalyst, but larger velocity can also be obtained with the MS catalyst when the pollutant is strongly adsorbed on this material. Moderate mineralization rates were observed for both catalysts illustrating the larger stability towards oxidation of the uncoloured organic intermediates resulting from the primary degradation of the model pollutants. Moreover the efficiency and stability of the MS catalyst were established since this material showed an activity for a pollutant during five consecutive tests. This was also confirmed by characterization of the catalyst after these tests. (C) 2013 Elsevier B.V. All rights reserved.
机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
BACRI, JC
PERZYNSKI, R
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机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
PERZYNSKI, R
SALIN, D
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机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
SALIN, D
CABUIL, V
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机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
CABUIL, V
MASSART, R
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机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
BACRI, JC
PERZYNSKI, R
论文数: 0引用数: 0
h-index: 0
机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
PERZYNSKI, R
SALIN, D
论文数: 0引用数: 0
h-index: 0
机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
SALIN, D
CABUIL, V
论文数: 0引用数: 0
h-index: 0
机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE
CABUIL, V
MASSART, R
论文数: 0引用数: 0
h-index: 0
机构:
UNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCEUNIV PIERRE & MARIE CURIE, PHYS CHIM INORGAN LAB, F-75252 PARIS 05, FRANCE