scholarly journals Comment on “Measurement and Modeling of Solubility of para-tert-Butylbenzoic Acid in Pure and Mixed Organic Solvents at Different Temperatures” and “Determination of Solubility and Thermodynamic Properties of Benzophenone in Different Pure Solvents”

Author(s):  
William E. Acree
2001 ◽  
Vol 33 (1) ◽  
pp. 47-59 ◽  
Author(s):  
F.Javier Carmona ◽  
Venkat R. Bhethanabotla ◽  
Scott W. Campbell ◽  
J. Antonio González, ◽  
Isaías García de la Fuente ◽  
...  

2017 ◽  
Vol 62 (9) ◽  
pp. 2676-2688 ◽  
Author(s):  
Clemente Bretti ◽  
Rosalia Maria Cigala ◽  
Francesco Crea ◽  
Concetta De Stefano ◽  
Giuseppe Gattuso ◽  
...  

2020 ◽  
Vol 13 (1) ◽  
pp. 25-29
Author(s):  
Tanaji N. Bansode

Potentiometric titrations of phenothiazines derivatives were performed in methanolwater, ethanol-water, acetonitrile-water and dioxane-water mixtures with varying contents of organic solvent. All titrations were performed in aqua-organic medium at constant ionic strength (0.15 mol⋅dm−3) and at different temperatures (25 to 45 °C). The pKa were determined at different aqua-organic proportions. Effect of temperature and dielectric constant on dissociation constant has been compared. The pKa values were then obtained by Yasuda‐Shedlovsky extrapolation.


1979 ◽  
Vol 44 ◽  
pp. 349-355
Author(s):  
R.W. Milkey

The focus of discussion in Working Group 3 was on the Thermodynamic Properties as determined spectroscopically, including the observational techniques and the theoretical modeling of physical processes responsible for the emission spectrum. Recent advances in observational techniques and theoretical concepts make this discussion particularly timely. It is wise to remember that the determination of thermodynamic parameters is not an end in itself and that these are interesting chiefly for what they can tell us about the energetics and mass transport in prominences.


1985 ◽  
Vol 54 (02) ◽  
pp. 533-538 ◽  
Author(s):  
Wilfried Thiel ◽  
Ulrich Delvos ◽  
Gert Müller-Berghaus

SummaryA quantitative determination of soluble fibrin in plasma was carried out by affinity chromatography. For this purpose, desAA-fibrin and fibrinogen immobilized on Sepharose 4B were used at the stationary side whereas batroxobin-induced 125I-desAA-fibrin or thrombin-induced 125I-desAABB-fibrin mixed with plasma containing 131I-fibrinogen represented the fluid phase. The binding characteristics of these mixtures to the immobilized proteins were compared at 20° C and 37° C. Complete binding of both types of fibrin to the immobilized desAA-fibrin was always seen at 20° C as well as at 37° C. However, binding of soluble fibrin was accompanied by substantial binding of fibrinogen that was more pronounced at 20° C. Striking differences depending on the temperature at which the affinity chromatography was carried out, were documented for the fibrinogen-fibrin interaction. At 20° C more than 90% of the applied desAA-fibrin was bound to the immobilized fibrinogen whereas at 37° C only a mean of 17% were retained at the fibrinogen-Sepharose column. An opposite finding with regard to the tested temperature was made with the desAABB-fibrin. Nearly complete binding to insolubilized fibrinogen was found at 37° C (95%) but only 58% of the desAABB-fibrin were bound at 20° C. The binding patterns did not change when the experiments were performed in the presence of calcium ions. The opposite behaviour of the two types of soluble fibrin to immobilized fibrinogen at the different temperatures, together with the substantial binding of fibrinogen in the presence of soluble fibrin to insolubilized fibrin in every setting tested, devaluates affinity chromatography as a tool in the quantitative assessment of soluble fibrin in patients’ plasma.


1960 ◽  
Vol XXXV (I) ◽  
pp. 34-48 ◽  
Author(s):  
Gerd Ittrich

ABSTRACT A series of organic solvents and phenol derivatives have been examined for the extraction of the pink Kober-colour complex. Optimal results could be achieved for fluorimetry by a solution of 2 % (w/v) p-nitrophenol and 1 % (v/v) ethanol in acetylenetetrabromide, when the green mercury line (546 mμ was used as primary light. The sensitivity, stability and specificity have been improved, compared with the previously described reaction. By changing the sequence of purification steps and by reducing the volume of the urine sample (5 ml) the method for the determination of total oestrogens has been simplified. Approximately 10 determinations can be done within 3–4 hours by one person. Recovery experiments and comparative determinations with a previously described method have been carried out. The excretion of total oestrogens in a complete menstrual cycle is determined with the described method.


2014 ◽  
Vol 32 (11) ◽  
pp. 1251
Author(s):  
Jing DA ◽  
Xianglu HUANG ◽  
Gangli WANG ◽  
Jin CAO ◽  
Qingsheng ZHANG

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