2016
DOI: 10.3906/kim-1507-7
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Preparation, characterization, and adsorption studies of core@shell SiO$_{2}$@CeO$_{2}$ nanoparticles: a new candidate to remove Hg(II) from aqueous solutions

Abstract: SiO 2 supported core@shell nanoparticles (CSNs) have recently attracted great attention due to their unique, tunable, optical, photocatalytic, and higher adsorption properties. In this study, SiO 2 @CeO 2 CSNs were synthesized using a chemical precipitation technique and characterized by Fourier transform infrared (FT-IR), X-ray diffraction (XRD), scanning electron microscope (SEM), and transmission electron microscope (TEM) analysis. XRD analysis showed that SiO 2 particles were the core while CeO 2 particles… Show more

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Cited by 5 publications
(5 citation statements)
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“…The peaks at 980 cm -1 and 854 cm -1 correspond to the asymmetric stretching vibration and symmetric stretching of Si-O-Si [35]. Moreover, the peak observed at 936 cm -1 should be due to the stretching vibration band of Ce-O-Si bonds [37], which reveals that Si 4+ is integrated into the surface of CeO2.…”
Section: Methodsmentioning
confidence: 96%
“…The peaks at 980 cm -1 and 854 cm -1 correspond to the asymmetric stretching vibration and symmetric stretching of Si-O-Si [35]. Moreover, the peak observed at 936 cm -1 should be due to the stretching vibration band of Ce-O-Si bonds [37], which reveals that Si 4+ is integrated into the surface of CeO2.…”
Section: Methodsmentioning
confidence: 96%
“…The XRD patterns of SiO 2 , C‐CTS, CTS‐S and C‐CTS‐S are presented in Figure . As shown in Figure , the broad peak is observed at about 22.31 ο belonging to the amorphous SiO 2 . The strong and broad bread peak at 10–30 ο of CTS‐S has a shift to a low angle (15.85 ο ) compared to pure SiO 2 , this could be attributed that the composite of SiO 2 and cross‐linked CTS leads to the lattice distortion of SiO 2 and significantly influences the crystal structure of the obtained products.…”
Section: Resultsmentioning
confidence: 95%
“…For the samples labeled C‐CTS‐S and C‐CTS, the amorphous phase can be identified by the fact that there are no sharp, single, intense and well recognizable peaks but only unclearly, low‐intense and broad recognizable peaks, it is the evidence of the disorder structure of the products containing Ce, which is demonstrated by SEM. The individual phases of Ce 2 O 3 and CeO 2 are not observed in C‐CTS and C–CTC−S, but there have appeared a peak at 26.68 ο in CTS‐S and C–CTC−S, which may be a new phase of Si species. The broad peak occurred at 20.54 ο in C‐CTS (see attached chart) resulted from the neat arrangement and crystallization of part of CTS molecular, and this peak is covered up by diffraction peak of SiO 2 in CTS‐S and shifts to 19.66 ο in C–CTC−S, which indicates that SiO 2 species not only stayed on the surface of CTS but entered its chain layer structure during the composite process.…”
Section: Resultsmentioning
confidence: 99%
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“…The decrease in the adsorption of adsorbate observed as the concentration (mg/L) increases might be attributed to the reduction of vacant sites on the adsorbents as they are completely filled with ions of adsorbate (Pb 2+ and Cd 2+ ). This indicates that uptake or efficiency of the adsorption process does not depend solely on adsorbent properties, but also on the initial adsorbate concentration (mg/L) in solution [12,29]. However, TbVI exhibited better uptake efficiency in Pb removal as the concentration of the adsorbate increases.…”
Section: Influence Of Parameters On Adsorption Experimentsmentioning
confidence: 92%