Preparation of Inverse Opal Zirconia

Authors

  • Xiao-peng Li Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science and Technology
  • Li-li Wang Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science and Technology
  • Zai-lei Gong Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science and Technology
  • Xiu-feng Wang Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science and Technology
  • Ye-ming Zhou Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry, Ministry of Education, Shaanxi University of Science and Technology

Abstract

Inverse opal zirconia is useful in many ways because of their ability to combine several chemical and physical properties. In this research, polystyrene template was fabricated by self-assembly method and inverse opal zirconia was prepared by colloidal crystal-templating method. The process of preparation of inverse opal zirconia as well as effects on morphology and phase of as-prepared inverse opal zirconia were studied. The results showed precursor ratio of zirconium acetate and methanol, mass ratio of polystyrene templates and precursor and dipping times had remarkable influence on morphology of inverse opal zirconia. When the precursor ratio was 1:1; the mass ratio was 1:15 and dipped once, much better morphology of inverse opal zirconia was obtained. The mass ratio, sintering temperature and holding time had significant effect on crystallization of zirconia. Pure phase zirconia could be obtained when sintered at 600 oC, holding time was 2h and the mass ratio was 1:1. A distinguished single stop band in the visible region of the spectrum and unique structural color were observed in inverse opal zirconia, which will make this material promising candidate for novel pigment.

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Published

2018-06-13

Issue

Vol. 50 No. 3 (2018)

Section

Articles

License

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