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April 22, 2026Molecules0 citationsOpen Access

High-Sensitivity Terahertz Time-Domain Spectroscopic Characterization of the Thermal Evolution of Hydrated Copper Sulfate

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YJYuqiu JiaoXLXinyu LiYZY X Zhang

Key Points

  • To investigate how water affects terahertz spectral responses during the thermal decomposition of hydrated copper sulfate.
  • Utilized terahertz time-domain spectroscopy to monitor thermal decomposition.
  • Examined variations in THz signals as water is removed from the copper sulfate lattice under heat.
  • THz signals show pronounced changes as copper sulfate hydrate loses water.
  • At around 60 °C, a strong THz absorption is observed, reflecting dynamic equilibrium between crystalline and free water.

Abstract

To elucidate the influence of water on terahertz (THz) spectral responses, terahertz time-domain spectroscopy (THz-TDS) was employed to monitor the thermal decomposition of copper(II) sulfate pentahydrate in this study. Continuous dehydration of the hydrate induces pronounced variations in the THz signal. At the initial stage of thermal decomposition, these changes primarily originate from the evolving state and amount of water confined within the CuSO4·5H2O lattice. After detaching from the crystalline framework, the released water molecules do not evaporate immediately; instead, they transiently reside near the copper sulfate as free water. When the temperature reaches approximately 60 °C, a dynamic equilibrium is established between crystalline water and free water. The THz spectral data reveal that the sample exhibits its strongest THz absorption at this temperature. Consequently, the THz signal during decomposition displays a characteristic trend: an initial decrease followed by an enhancement. These findings demonstrate that THz-TDS represents a promising approach for probing the state and content of water, thereby contributing to the development of a powerful analytical tool for fundamental studies in mineralogy.

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Cite This Study

Jiao et al. (2026) studied this question.

synapsesocial.com/papers/69e866ad6e0dea528ddeb15ahttps://doi.org/10.3390/molecules31081342
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