Evaluation of changing the structure of aqueous solutions in the near-wall layers with using dielectrometry and resonance method

2015 ◽  
Vol 9 (2) ◽  
pp. 0-0
Author(s):  
Саркисов ◽  
Yu. Sarkisov ◽  
Сидоренко ◽  
G. Sidorenko ◽  
Лаптев ◽  
...  

In this work the authors evaluated changes of the structure of aqueous solutions of chlorides of sodium and potassium in various concentrations in the parietal layer by means of the dielectrometry and resonance method. In experiments at 20 ° C, the concentration of sodium and potassium chloride concentration of 0.01 M to 1 M in thenear-wall layer "glass - water solutions" height of less than 1000 microns observed multiple reduction of capacitance of solutions, and Q of an oscillatory circuit and a multiple increase coefficient KS which allows to evaluate the structure of the solutions. It is shown that the structure of the solutions in the wall layer depends on the solution concentration, the nature of the solute and the material of surface. Methods of dielectrometry and resonance are informative in the interpretation of the processes in the fluid layer at the interface, "solid – aqueous solution".

1984 ◽  
Vol 49 (3) ◽  
pp. 559-569 ◽  
Author(s):  
Jaroslav Nývlt

The metastable zone width of an aqueous solution of KCI was measured as a function of the time and temperature of overheating above the equilibrium solubility temperature. It has been found that when the experiments follow close upon one another, the parameters of the preceding experiment affect the results of the experiment to follow.The results are interpreted in terms of hypotheses advanced in the literature to account for the effect of thermal history of solution. The plausibility and applicability of these hypotheses are assessed for the given cause of aqueous solution of a well soluble electrolyte.


1879 ◽  
Vol 29 (196-199) ◽  
pp. 472-482 ◽  

In order to investigate this subject, I devised and constructed the following apparatus :—A and B are two thin glass basins, 81 millims. internal diameter (= 5,153 sq. millims. of mercury surface), and 6·0 centims. deep; each containing a layer of mercury about 1·0 centim. deep, covered by a layer, about 3 centims. deep, of the aqueous solution to be examined.


2021 ◽  
Author(s):  
Junyi Li ◽  
Zoltán Szabó ◽  
Mats Jonsson

Four different uranyl-(peroxide)-carbonate complexes were identified during studtite and meta-studtite dissolution in aqueous solution containing 10 mM HCO3− by 13C NMR.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Zhirayr Baghdasaryan ◽  
Arsen Babajanyan ◽  
Levon Odabashyan ◽  
Jung-Ha Lee ◽  
Barry Friedman ◽  
...  

AbstractIn this study, a new optical method is presented to determine the concentrations of NaCl and glucose aqueous solutions by using a thermo-elastic optical indicator microscope. By measuring the microwave near-field distribution intensity, concentration changes of NaCl and glucose aqueous solutions were detected in the 0–100 mg/ml range, when exposed to microwave irradiation at 12 GHz frequency. Microwave near-field distribution intensity decreased as the NaCl or glucose concentration increased due to the changes of the absorption properties of aqueous solution. This method provides a novel approach for monitoring NaCl and glucose in biological liquids by using a CCD sensor capable of visualizing NaCl and glucose concentrations without scanning.


2021 ◽  
Author(s):  
Liang Wang ◽  
Peng Gao ◽  
Mengxin Liu ◽  
Ziqing Huang ◽  
Shixia Lan ◽  
...  

Monodisperse polypyrrole/SBA-15 composite (PPy/SBA-15) was fabricated by in-situ polymerization and used for Cr(Ⅵ) adsorption from aqueous solution. PPy/SBA-15 was characterized by numerous approaches. Factors affecting the Cr(Ⅵ) adsorption process included...


1989 ◽  
Vol 42 (3) ◽  
pp. 365 ◽  
Author(s):  
MK Manthey ◽  
SG Pyne ◽  
RJW Truscott

The oxidation of catechol in the presence of two aliphatic and aromatic amines has been investigated. In aqueous solutions of pH 7.0 and 11.7, the substitution pattern of the adduct was dependent on the type of amine used. Aromatic amines produced 4,5-disubstituted o-quinones, whereas aliphatic amines gave either 2,4,5-trisubstituted or 2,4-disubstituted o-quinone adducts. A rationale based upon the stability of vinylogous amides is presented to account for the observed substitution pattern.


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