Abstract

We have made investigations of the phase formation and microstructure on the ceramics obtained from a starting nanopowder mixture with the weight ratio ZnO : TiO2 = 4 : 1. Ceramic is obtained at different sintering temperatures, namely, 948, 1223 and 1473 ?. Using the characterization methods of electron microscopy, energy dispersive microanalysis and X-ray diffraction phase analysis it has been shown that the ceramics structure is consisted of two dispersed phases of Zn2TiO4 and ZnO with the grain sizes being in range 0,5-1 ?m. It has been found also that, at ceramic`s sintering temperature of 1223 ?, the solid phase interactions are completed with the structure ZnO : Zn2TiO4 ? 1 : 1,5 phase ratio.

Highlights

  • Nanostructures based on zinc and titanium oxides attract attention due to their peculiar structural, optical, optoelectronic and other characteristics

  • Observed two phase ceramics were obtained by solid phase sintering of the nanopowder mixture of ZnO and TiO2

  • The initial stage of sintering is found to be at 948 К and it is declared with forming neck contacts between dispersed powder particles inside the nanopowder agglomerates

Read more

Summary

Introduction

Nanostructures based on zinc and titanium oxides attract attention due to their peculiar structural, optical, optoelectronic and other characteristics. Compounds based on ZnO-TiO2 (zinc titanates) are technologically important since they possess specific properties hardly obtained using solely ZnO. In the ZnO–TiO2 system six chemical compounds of various types are formed, where ortho- and metatitanate are the best studied [4,5,6]. Zinc orthotitanate Zn2TiO4 occurs in the form of crystals having cubic regular octahedra structure with the lattice parameter being а = 0,846 nm. The obtained compounds of zinc orthotitanate are found to be stable to temperature changes. Zinc metatitanate ZnTiO3 occurs as hexagonal system crystals – ilmenite wit the lattice parameters being а = 0,508 nm and с = 1,392 nm

Objectives
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.