SATIE, IFSTTAR, University Gustave Eiffel, Campus de Marne-La-Vallée, 25, allée des Marronniers, 78000 Versailles, France.
Laboratory of Materials, Catalysis, Environment and Analytical Methods (MCEMA) and LEADDER Laboratory, Faculty of Sciences and EDST, Lebanese University, Hariri Campus, Hadath, P.O. Box 6573/14, Beirut, Lebanon.
J Chromatogr Sci. 2022 Feb 16;60(2):126-142. doi: 10.1093/chromsci/bmab066.
A new methodology was proposed to determine the dispersive component of the surface energy ${\gamma}s^d$ of a solid taking into account the effect of the temperature on the surface area of n-alkanes, methylene group (${a}{- CH2-}$) and polar molecules, thus defeating the method used by Dorris-Gray Schultz et al. We determined the correct ${\gamma}_s^d$ of the surface energy, the specific free energy, enthalpy and entropy of adsorption of polar molecules as well as the acid base constants of silica particles with an excellent accuracy. We confirmed the dependence of the dispersive component of the surface energy on the variations of the surface areas of organic molecules used in IGC technique at infinite dilution. The specific properties of interactions of silica particles were determined. The new proposed model took into account this thermal effect. Obtained results proved that the other used IGC methods gave inaccurate values of the specific parameters of silica surface, except for the vapor pressure method that led to excellent results of the specific free energy, enthalpy and entropy of adsorption, and the acid-base constants of the silica particles.
提出了一种新的方法来确定固体的表面能分散分量${\gamma}s^d$,该方法考虑了温度对 n-烷烃、亚甲基(${a}{- CH2-}$)和极性分子表面积的影响,从而克服了 Dorris-Gray Schultz 等人使用的方法。我们确定了极性分子的正确表面能分散分量${\gamma}_s^d$、比吸附自由能、焓和熵以及具有优异精度的硅粒子的酸碱常数。我们证实了表面能分散分量随 IGC 技术中无限稀释时使用的有机分子表面积的变化而变化。确定了硅粒子相互作用的特定性质。新提出的模型考虑了这种热效应。得到的结果证明,除了蒸汽压法导致硅粒子的比吸附自由能、焓和熵以及酸碱常数的优异结果外,其他使用的 IGC 方法给出了硅表面的比参数的不准确值。