Solubility Constant

2016 ◽  
Author(s):  
Heinz Gamsjäger ◽  
John W. Lorimer ◽  
Pirketta Scharlin ◽  
David G. Shaw
Keyword(s):  
Minerals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 135
Author(s):  
Justyna Topolska ◽  
Bartosz Puzio ◽  
Olaf Borkiewicz ◽  
Julia Sordyl ◽  
Maciej Manecki

Although vanadinite (Pb5(VO4)3Cl) occurs in abundance in various terrestrial geochemical systems of natural and anthropogenic origin and is seriously considered as a potential nuclear waste sequestering agent, its actual application is severely limited by a lack of understanding of its basic thermodynamic parameters. In this regard, the greatest challenge is posed by its incongruent dissolution, which is a pivotal hurdle for effective geochemical modeling. Our paper presents an universal approach for geochemical computing of systems undergoing incongruent dissolution which, along with unique, long-term experiments on vanadinites’ stability, allowed us to determine the mineral solubility constant. The dissolution experiments were carried out at pH = 3.5 for 12 years. Vanadinite has dissolved incongruently, continuously re-precipitating into chervetite (Pb2V2O7) with the two minerals remaining in mutual equilibrium until termination of the experiments. The empirically derived solubility constant Ksp,V,298 = 10–91.89 ± 0.05 of vanadinite was determined for the first time. The proposed modeling method is versatile and can be adopted to other mineral systems undergoing incongruent dissolution.


2019 ◽  
Vol 203 ◽  
pp. 86-103 ◽  
Author(s):  
Helei Liu ◽  
Raphael Idem ◽  
Paitoon Tontiwachwuthikul
Keyword(s):  

2013 ◽  
Vol 85 (11) ◽  
pp. 2051-2058 ◽  
Author(s):  
Alex De Visscher ◽  
Maria S. Conejo

Capturing CO2 emissions from energy production and storing it under the ground is a potential CO2 mitigation strategy that currently receives much attention. Both CO2 capture and CO2 storage are solubility problems. This paper reviews some important solubility aspects of CO2 capture and storage that are often overlooked. Until very recently, there was not a single CO2 solubility relationship that was both applicable in a wide temperature range and thermodynamically consistent with the enthalpy of solution of CO2. Furthermore, very often the relationship used for the first acidity constant of carbonic acid as a function of temperature is inconsistent with the relationship used for the solubility constant (or Henry constant) of CO2. The removal of CO2 from a gas stream with amine solutions is usually viewed as a chemical reaction, which leads to the practice of heating to remove the CO2 from the solvent. However, viewing this process as a solubility phenomenon suggests the practice of using vacuum to remove the CO2 from the solvent, a potentially more efficient approach.


2008 ◽  
Vol 72 (2) ◽  
pp. 343-346 ◽  
Author(s):  
Mauro Iuliano ◽  
Liberato Ciavatta ◽  
Gaetano De Tommaso
Keyword(s):  

Clay Minerals ◽  
1998 ◽  
Vol 33 (1) ◽  
pp. 77-86 ◽  
Author(s):  
J. P. Gustafsson ◽  
D. G. Lumsdon ◽  
M. Simonsson

AbstractFifteen Swedish and Finnish soil samples from spodic B horizons containing imogolite-type materials were equilibrated with dilute NaCl and HC1 at 8°C. For the NaCl extracts, apparent equilibrium with respect to an AI(OH)3 phase was reached in one to two weeks. Equilibrium with respect to an imogolite-type phase was slower, especially at large soil:solution ratios. The results show that log *Ks (gibbsite), i.e. the logarithm of the solubility constant for reactive AI(OH)3 at 8°C was ~9.40 (8.29 at 25°C) while log *Ks (imogolite) was variable; for the soil studied in most detail it was 7.66 (6.64 at 25°C) As well-ordered gibbsite rarely forms in spodic B horizons, it is suggested that Al(OH)3 and poorly-ordered allophanic materials may be slowly converted to less soluble and less reactive imogolite-type materials.


1998 ◽  
Vol 13 (1) ◽  
pp. 16-21 ◽  
Author(s):  
S. Gñni ◽  
A. Macías ◽  
J. Madrid ◽  
J. M. Díez

Mixtures of CaO–CdO (1 : 1) were hydrothermally treated in a pressure reactor at 200 °C and 200 psi of pressure during a period of 16 h. The evolution of the reaction was followed by x-ray diffraction (XRD), infrared spectroscopy (IR), and thermogravimetric (TG and DTG) analysis. Also, the composition of the filtered solutions was analyzed to determine the mechanism of the reaction as well as the thermodynamic solubility constant of the new compound formed. The results show that CaO and CdO react, giving rise to a new CaCd(OH)4 hydroxide whose thermodynamic solubility constant, 1.5 ± 0.4 × 10−11 M2, is six orders of magnitude lower than those of both Ca(OH) 2 and β–Cd(OH) 2. This low solubility constant justifies the Cd2+ concentration measured in the pore solution of cement matrices used to immobilize cadmium containing wastes. The mechanism of the reaction proposed is via dissolution of both Ca(OH) 2 and β–Cd(OH)2, Ca2+ and being the predominant species in solution.


2007 ◽  
Vol 71 (4) ◽  
pp. 1137-1140 ◽  
Author(s):  
Mauro Iuliano ◽  
Liberato Ciavatta ◽  
Gaetano De Tommaso
Keyword(s):  

1988 ◽  
Vol 127 ◽  
Author(s):  
Kaija Olliia

ABSTRACTThe solubilities of uranium measured in deionized water, in sodium bicarbonate solutions as a function of carbonate concentration and in two types of synthetic groundwaters have been compared with those predicted using the reaction pathway program, PHREEQE. All the measurements were carried out under both air-saturated, oxidizing and anoxic, reducing conditions.The experimental solubility values of uranium under oxidizing conditions are, in general, lower when compared to the corresponding theoretical ones calculated by PHREEQE. A critical factor is the choice of solubility constant for the solid phase. The reason for the lower solubility values may also be the mechanism of dissolution leading for example either to a situation where low dissolution rate is a limiting factor, or to formation of some solid phase of uranium with lower solubility. The experimental solubility values under reducing conditions appear to be in good agreement with the theoretical solubility values.


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