scholarly journals Solutions, in Particular Dilute Solutions of Nonelectrolytes: A Review

Author(s):  
Emmerich Wilhelm

AbstractThe liquid state is one of the three principal states of matter and arguably the most important one; and liquid mixtures represent a large research field of profound theoretical and practical interest. This topic is of importance in many areas of the applied sciences, such as in chemical engineering, geochemistry, the environmental sciences, biophysics and biomedical technology. First, I will concisely present a review of important concepts from classical thermodynamics of nonelectrolyte solutions; this will be followed by a survey of (semi-)empirical approaches to representing the composition and temperature dependence of selected thermodynamic mixture properties, and finally the focus will be on dilute binary nonelectrolyte solutions where one component, a supercritical solute, is present in much smaller quantity than the other component, called the solvent. Partial molar properties in the limit of infinite dilution (indicated by a superscript ∞) are of particular interest. For instance, activity coefficients (Lewis–Randall (LR) convention) are customarily used to characterize mixing behavior, and infinite-dilution values $$\gamma_{i}^{{{\text{LR,}}\infty }}$$ γ i LR, ∞ provide a convenient route for obtaining binary parameters for several popular solution models. When discussing solute (j)—solvent (i) interactions in solutions where the solute is supercritical, the Henry fugacity $$h_{j,i} \left( {T,P} \right)$$ h j , i T , P , also known as Henry’s law (HL) constant, is a measurable thermodynamic key quantity. Its temperature dependence yields information on the partial molar enthalpy change on solution $$\Delta H_{j}^{\infty } \left( {T,P} \right)$$ Δ H j ∞ T , P , while its pressure dependence yields information on the partial molar volume $$V_{j}^{{{\text{L,}}\infty }} \left( {T,P} \right)$$ V j L, ∞ T , P of solute j in the liquid phase (superscript L). I will clarify issues frequently overlooked, touch upon solubility data reduction and correlation, report a few recent high-precision experimental results on dilute aqueous solutions of supercritical nonelectrolytes, and show the equivalency of results for caloric quantities (e.g. $$\Delta H_{j}^{\infty }$$ Δ H j ∞ ) obtained via van ’t Hoff analysis of high-precision solubility data with directly measured calorimetric data.

2013 ◽  
Vol 85 (11) ◽  
pp. 2097-2116 ◽  
Author(s):  
Pengsheng Song ◽  
Bai Sun ◽  
Dewen Zeng

Solubility equilibria are relevant to many aspects of chemistry and chemical engineering. Studies on solubility phenomena are of importance in understanding chemistry and in the development of chemical technology. Solubility equilibria are especially useful for geochemists investigating the formation and evolution of natural salt deposits. China possesses an enormous variety of such resources, including salt lakes, underground brines, oilfield brines, and natural soda and borate deposits, etc. With the ongoing economic development of China, the exploitation and comprehensive utilization of these kinds of mineral resources are making great progress. Although much research on aqueous salt systems has been published, solubility equilibria studies have long been an active research field in China. This paper presents a review of solubility research on salt/water systems, encompassing more than 200 papers from Chinese researchers.


2015 ◽  
Vol 37 (5-6) ◽  

In the 1970s, IUPAC’s Solubility Data Commission (now the Subcommittee on Solubility and Equilibrium Data) embarked on a project to compile and critically evaluate experimental data for solubility in systems of scientific and practical interest. The first volume in the IUPAC Solubility Data Series, covering the solubility of helium and neon in liquid solvents, was published in 1979. Subsequent years saw many volumes on gas-liquid, liquid-liquid, and solid-liquid solubilities. These volumes are an invaluable scientific resource.


2008 ◽  
Vol 354 (34) ◽  
pp. 4094-4100 ◽  
Author(s):  
Yaron Greenberg ◽  
Eyal Yahel ◽  
Moshe Ganor ◽  
Refael Hevroni ◽  
Igor Korover ◽  
...  

1996 ◽  
Vol 453 ◽  
Author(s):  
Z. -Y. Cheng ◽  
R. S. Katiyar ◽  
Yao Xi

AbstractAddition to thermally activated flips of polar regions in relaxor ferroelectrics, a new polarization mechanism, which originates from the vibrations (breathing) of surface of polar regions, is introduced to explain the dielectric behavior of relaxor ferroelectrics. This new mechanism plays an important role in the dielectric behavior of such materials at low temperature. Based on the above assumption and general dielectric theory, a formula is given to characterize the temperature dependence of the dielectric constant. The correctness of the formula is verified by using it to fit the experimental results of the two typical relaxors. The fitted results show that the method is of high precision and that the temperature of the dielectric constant maximum is decided by the two polarization behavior. It also indicates that the new polarization is a resonance polarization.


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