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Chinese Journal of Materials Research  2016, Vol. 30 Issue (5): 365-371    DOI: 10.11901/1005.3093.2015.440
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Ceria Hollow Nanospheres Synthesized by Hydrothermal Method and Their Adsorption Capacity
ZHANG Jiao, JIANG Xueliang**(), YU Lu, CHEN Jiangtao
School of Materials Science and Engineering, Wuhan Institute of Technology, Wuhan 430073, China
Cite this article: 

ZHANG Jiao, JIANG Xueliang, YU Lu, CHEN Jiangtao. Ceria Hollow Nanospheres Synthesized by Hydrothermal Method and Their Adsorption Capacity. Chinese Journal of Materials Research, 2016, 30(5): 365-371.

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Abstract  

Uniform-sized and monodisperse ceria (CeO2) hollow nanospheres were synthesized in a ethylene glycol aqueous solution with cerium nitrate hexahydrate (Ce(NO3)3·6H2O) as cerium sources and polyvinylpyrrolidone (PVP) as surfactant. The synthesized products were characterized by means of Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoelectron spectrum (XPS), X-ray diffraction (XRD), N2 adsorption-desorption and UV-Vis. The results show that the porous CeO2 hollow nanospheres composed of small nanoparticles with cubic fluorite structure; the average diameter and wall thickness of the CeO2 hollow nanospheres were about 400nm and 30 nm respectively; they have a high specific surface area of 76.86 m2g-1 and BJH pore size about 3~5 nm. On the basis of time-dependent experiment, the relevant formation mechanism was proposed. The ceria hollow nanospheres show an excellent adsorption rate about 70% of heavy metal ions at room temperature for Cr(VI) solutions, which is 3 times higher than that of ceria powder.

Key words:  metallic materials      ceria hollow nanospheres      hydrothermal method      adsorption capacity     
Received:  04 August 2015     
ZTFLH:  TB383  
Fund: *Supported by National Natural Science Foundation of China No.51273154, the Natural Science Foundation of Hubei No.2011CBD220, the Graduate Student Education Innovation Foundation of Wuhan Institute of Technology No.CX2014064
About author:  **To whom correspondence should be addressed, Tel: 15802730640, E-mail: sjtujxl@163.com

URL: 

https://www.cjmr.org/EN/10.11901/1005.3093.2015.440     OR     https://www.cjmr.org/EN/Y2016/V30/I5/365

Fig.1  FT-IR spectra of the precursor (a) and CeO2 hollow spheres after calcination (b)
Fig.2  XRD spectra of the precursor (a) and CeO2 hollow spheres (b)
Fig.3  SEM (a) and TEM (b) images of the obtained ceria hollow spheres
Fig.4  SEM and TEM images of the obtained CeO2 samples collected at different reaction time (a, b) 6 h; (c, d) 12 h; (e, f) 16 h; (g, h) 22 h
Fig.5  XPS wide spectrum (a) and Ce3d spectrum (b) of CeO2 hollow nanospheres
Fig.6  N2 adsorption-desorption isotherm of the CeO2 hollow spheres (a) and the corresponding BJH pore size distribution curve (b)
Fig.7  Schematic illustration of the formation of the CeO2 hollow spheres
Fig.8  The absorption rate curve of Cr(VI) solutions at different time (a) CeO2 powder, (b) the precursor, and (c) CeO2 hollow spheres
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