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Vapor Pressure and Enthalpy of Vaporization of Guanidinium Methanesulfonate as a Phase Change Material for Thermal Energy Storage.
Bi, Wenrong; Liu, Shijie; Rong, Xing; Ma, Guangjun; Luo, Jiangshui.
Affiliation
  • Bi W; Laboratory of Electrolytes and Phase Change Materials, College of Materials Science and Engineering, Sichuan University, Chengdu 610065, China.
  • Liu S; Laboratory of Electrolytes and Phase Change Materials, College of Materials Science and Engineering, Sichuan University, Chengdu 610065, China.
  • Rong X; Laboratory of Electrolytes and Phase Change Materials, College of Materials Science and Engineering, Sichuan University, Chengdu 610065, China.
  • Ma G; Laboratory of Electrolytes and Phase Change Materials, College of Materials Science and Engineering, Sichuan University, Chengdu 610065, China.
  • Luo J; Laboratory of Electrolytes and Phase Change Materials, College of Materials Science and Engineering, Sichuan University, Chengdu 610065, China.
Materials (Basel) ; 17(11)2024 May 27.
Article in En | MEDLINE | ID: mdl-38893846
ABSTRACT
This paper reports the vapor pressure and enthalpy of vaporization for a promising phase change material (PCM) guanidinium methanesulfonate ([Gdm][OMs]), which is a typical guanidinium organomonosulfonate that displays a lamellar crystalline architecture. [Gdm][OMs] was purified by recrystallization. The elemental analysis and infrared spectrum of [Gdm][OMs] confirmed the purity and composition. Differential scanning calorimetry (DSC) also confirmed its high purity and showed a sharp and symmetrical endothermic melting peak with a melting point (Tm) of 207.6 °C and a specific latent heat of fusion of 183.0 J g-1. Thermogravimetric analysis (TGA) reveals its thermal stability over a wide temperature range, and yet three thermal events at higher temperatures of 351 °C, 447 °C, and 649 °C were associated with vaporization or decomposition. The vapor pressure was measured using the isothermogravimetric method from 220 °C to 300 °C. The Antoine equation was used to describe the temperature dependence of its vapor pressure, and the substance-dependent Antoine constants were obtained by non-linear regression. The enthalpy of vaporization (ΔvapH) was derived from the linear regression of the slopes associated with the linear temperature dependence of the rate of weight loss per unit area of vaporization. Hence, the temperature dependence of vapor pressures ln Pvap (Pa) = 10.99 - 344.58/(T (K) - 493.64) over the temperature range from 493.15 K to 573.15 K and the enthalpy of vaporization ΔvapH = 157.10 ± 20.10 kJ mol-1 at the arithmetic mean temperature of 240 °C were obtained from isothermogravimetric measurements using the Antoine equation and the Clausius-Clapeyron equation, respectively. The flammability test indicates that [Gdm][OMs] is non-flammable. Hence, [Gdm][OMs] enjoys very low volatility, high enthalpy of vaporization, and non-flammability in addition to its known advantages. This work thus offers data support, methodologies, and insights for the application of [Gdm][OMs] and other organic salts as PCMs in thermal energy storage and beyond.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Materials (Basel) Year: 2024 Document type: Article Affiliation country: China Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Materials (Basel) Year: 2024 Document type: Article Affiliation country: China Country of publication: Suiza