Surface nucleation and independent growth of Ce(OH)4 within confinement space on modified carbon black surface to prepare nano-CeO2 without agglomeration

Xinyue ZHANG, Chunhui XIA, Kaitao LI, Yanjun LIN

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Front. Mater. Sci. ›› 2018, Vol. 12 ›› Issue (2) : 168-175. DOI: 10.1007/s11706-018-0421-4
RESEARCH ARTICLE
RESEARCH ARTICLE

Surface nucleation and independent growth of Ce(OH)4 within confinement space on modified carbon black surface to prepare nano-CeO2 without agglomeration

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Abstract

Highly dispersed negative carboxyl groups can be formed on carbon black (CB) surface modified with strong nitric acid. Therefore positive cations can be uniformly absorbed by carboxyl groups and precipitated within a confinement space on modified CB surface to prepare highly dispersed nanomaterials. In this paper, the formation and dispersion status of surface negative carboxyl groups, adsorption status of Ce3+, surface confinement nucleation, crystallization and calcination process were studied by EDS, SEM, and laser particle size analysis. The results show that the carboxyl groups formed on modified CB surface are highly dispersed, and Ce3+ cations can be uniformly anchored by carboxyl groups. Therefore, highly dispersed Ce3+ can react with OH within a confinement surface region to form positive nano-Ce(OH)4 nuclei which also can be adsorbed by electrostatic attraction. After independent growth of Ce(OH)4 without agglomeration, highly dispersed CeO2 nanoparticles without agglomeration can be prepared together with the help of effectively isolates by CO2 released in the combustion of CB.

Keywords

surface nucleation / confinement space / modified CB / agglomeration / nano-CeO2

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Xinyue ZHANG, Chunhui XIA, Kaitao LI, Yanjun LIN. Surface nucleation and independent growth of Ce(OH)4 within confinement space on modified carbon black surface to prepare nano-CeO2 without agglomeration. Front. Mater. Sci., 2018, 12(2): 168‒175 https://doi.org/10.1007/s11706-018-0421-4

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Acknowledgements

This work was supported by the National Key R&D Program of China (2016YFB0301602) and the National Natural Science Foundation of China (Grant Nos. 21776018 and 21627813).

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2018 Higher Education Press and Springer-Verlag GmbH Germany, part of Springer Nature
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