Research Article
BibTex RIS Cite

SYNTHESIS AND CHARACTERIZATION OF A NEW COBALT POLYMERIC SPINELS

Year 2003, Volume: 49 , 0 - 0, 01.01.2003
https://doi.org/10.1501/Commub_0000000360

Abstract

Some cobalt spinels were synthesized under hydrothermal conditions, starting from metal chlorides, and Poly N-Acrolylquinazoline. The color properties in these systems mainly depend upon the preparative method and cation distributions, which have been determined by visible and near infrared absorption spectra. We observe the influence of tetrahedral and octahedral preference of cations such as Co2+, Cr3+, Mn3+ upon the formation and the color development of cobalt spinel polymers. All the samples prepared revealed the formation of single spinel with particle size at about 0.8-2.1 /J m; COAI2O4 reveals kings blue, CoMn2O4 dark blue and CoCr2O4 bluish green. Cobalt blues developed giving deep absorption characteristic of tetrahedral Co2+ ions at about 550-680 nm; therefore, color changed from kings blue to bluish green in CoCr2O4, showing the absorption band of octahedral Cr3+ ions owing to the large excess octahedral crystal field stabilization energy.

References

  • Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
Year 2003, Volume: 49 , 0 - 0, 01.01.2003
https://doi.org/10.1501/Commub_0000000360

Abstract

References

  • Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
There are 1 citations in total.

Details

Primary Language English
Subjects Chemical Engineering
Journal Section Research Article
Authors

A. Al-thabaıtı Shaeel This is me

Publication Date January 1, 2003
Published in Issue Year 2003 Volume: 49

Cite

Vancouver Shaeel AA-t. SYNTHESIS AND CHARACTERIZATION OF A NEW COBALT POLYMERIC SPINELS. Commun. Fac. Sci. Univ. Ank. Ser. B. 2003;49.

Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.