Comparison of Polythionates as Precursors for the Formation of Thallium Sulfide Layers

Authors

  • Vitalijus JANICKIS Kaunas University of Technology
  • Rūta STOKIENĖ Kaunas University of Technology
  • Nijolė KREIVĖNIENĖ Kaunas University of Technology

DOI:

https://doi.org/10.5755/j01.ms.17.4.774

Keywords:

polythionates, polyamide, sorption-diffusion, thallium sulfide layers

Abstract

The processes of obtaining layers of thallium, sulfides, TlxSy, by the sorption-diffusion method on polyamide 6 using solutions of lower polythionates - sodium trithionate and tetrathionate, Na2S3O6, Na2S4O6, potassium pentathionate, K2S5O6, and of dodecathionic acid, H2S12O6, as precursors of sulfur are compared. The concentration of sorbed sulfur increases with increasing the duration of treatment, the concentration and temperature of precursor solution. It rather significantly also depends on the nature - sulfurity of polythionate, i. e. on the number of sulfur atoms in the polythionate anion: effectiveness of sulfurization using solutions of dodecathionic acid is significantly higher than that of lower polythionates. Thallium sulfide layers are formed on the surface of polyamide after the treatment of sulfurized polymer with Tl(I) salt solution. The concentration of thallium in the layer increases with the increase of initial sulfurization duration and in case of H2S12O6 solution used - on the temperature of this process. The results of X-ray diffraction analysis confirmed the formation of thallium sulfide layers in the surface of polyamide 6. The phase composition of layer changes depending on the conditions of initial treatment in a H2S12O6 solution. Five thallium sulfide phases, two forms of TlS, Tl2S2, Tl4S3 and Tl2S5 were identified in the composition of the layers treated for different time with a solution of dodecathionic acid at the temperature of 20 °C and 30 °C and then with Tl(I) salt solution by X-ray diffraction but the maxima of TlS and Tl2S5 phases predominate in the diffractograms.

http://dx.doi.org/10.5755/j01.ms.17.4.774

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Published

2011-11-18

Issue

Section

POLYMERS AND COMPOSITES