Abstract <p>As a result of the analysis of data from literature sources, the average values of the reaction rate constant for the dissolution of gypsum in water (<i>k</i><sub>av</sub> = 1.48 × 10<sup>–5</sup> mmol/(cm<sup>2</sup> s, 25°C) and activation energy (<InlineEquation ID="IEq1"> <InlineMediaObject> <ImageObject Color="BlackWhite" FileRef="11969_2025_7468_Article_IEq1.gif" Format="GIF" Height="20" Rendition="HTML" Resolution="72" Type="Linedraw" Width="26" /> </InlineMediaObject> <EquationSource Format="TEX">\(E_{{{\text{av}}}}^{1}\)</EquationSource> <!--BGeoMGU2570030Lebedev-m1--> </InlineEquation>&#xa0;= 39&#xa0;kJ/mol), characteristic of kinetic and diffusion-kinetic control conditions, were determined. The calculated temperature dependence follows the Arrhenius equation in the range 0–40°C (log <i>k</i><sub>av</sub> = 1.95–2021/<i>T</i>, К). An increase in solution temperature (<i>T</i> &gt; 40°C) causes diffusion inhibition of heterogeneous chemical reactions of gypsum dissolution. It is assumed that at <i>T</i> ≈ 40–42°C the boundary between the macrokinetic regions of gypsum dissolution in water corresponds to the zone of temperature transition between the equilibrium state of gypsum and anhydrite (CaSO<sub>4</sub>⋅2H<sub>2</sub>O<sup>s</sup>–<InlineEquation ID="IEq2"> <InlineMediaObject> <ImageObject Color="BlackWhite" FileRef="11969_2025_7468_Article_IEq2.gif" Format="GIF" Height="18" Rendition="HTML" Resolution="72" Type="Linedraw" Width="49" /> </InlineMediaObject> <EquationSource Format="TEX">\({\text{CaSO}}_{4}^{{\text{s}}}\)</EquationSource> <!--BGeoMGU2570030Lebedev-m2--> </InlineEquation>–H<sub>2</sub>O; <i>P</i> = 0.1 MPa). It is proposed that a similar transition in electrolyte solutions should also be determined taking the diffusion resistance of the rate of chemical interactions on the reaction gypsum surface with increasing solution temperature into account.</p>

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The Temperature Dependence of the Rate Constant of the Reaction of Gypsum Dissolution in Water

  • A. L. Lebedev,
  • I. V. Avilina

摘要

Abstract

As a result of the analysis of data from literature sources, the average values of the reaction rate constant for the dissolution of gypsum in water (kav = 1.48 × 10–5 mmol/(cm2 s, 25°C) and activation energy ( \(E_{{{\text{av}}}}^{1}\)  = 39 kJ/mol), characteristic of kinetic and diffusion-kinetic control conditions, were determined. The calculated temperature dependence follows the Arrhenius equation in the range 0–40°C (log kav = 1.95–2021/T, К). An increase in solution temperature (T > 40°C) causes diffusion inhibition of heterogeneous chemical reactions of gypsum dissolution. It is assumed that at T ≈ 40–42°C the boundary between the macrokinetic regions of gypsum dissolution in water corresponds to the zone of temperature transition between the equilibrium state of gypsum and anhydrite (CaSO4⋅2H2Os \({\text{CaSO}}_{4}^{{\text{s}}}\) –H2O; P = 0.1 MPa). It is proposed that a similar transition in electrolyte solutions should also be determined taking the diffusion resistance of the rate of chemical interactions on the reaction gypsum surface with increasing solution temperature into account.