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Temperature-modulated DSC TOPEM ® method was applied to study amorphization in directly synthesized high-temperature polymorph of tetra-arsenic tetra-sulfide β-As 4 S 4 affected to high-energy mechanical milling in a dry mode with 100–600 min −1 rotational speeds. The appeared amorphous phase is shown to possess dual nature, being related to As-rich glassy-like substances with low- and high-temperature glass transition midpoints. In respect of DSC TOPEM ® studies, the crystalline–amorphous heterogeneity of chemical environment around β-As 4 S 4 crystallites results in incongruent double-peak melting revealed through two endothermic effects at~ 305 °C and ~ 315 °C. Amorphous phase continuously generated under ball milling with increased rotational speed is identified as compositionally authentic to arsenic monosulfide, but different in medium-range order from stoichiometric As 2 S 3 . The overall amorphization in commercial arsenic sulfide prepared by direct synthesis from elemental constituents under high-energy ball milling occurs from two sources, these being high-to-low- T g amorphous phase transformation and direct vitrification of β-As 4 S 4 phase. These data testifies in favor of “shell” model treated solid-state amorphization in terms of defect generation in parent β-As 4 S 4 phase, the amorphous substance being nucleated heterogeneously from grain boundaries followed by stretching into crystalline grain interior.
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Shpotyuk et al. (2018) studied this question.
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