Filtration of an aqueous salt solution in capillary-porous materials in the presence of a phase transition

1987 ◽  
Vol 52 (2) ◽  
pp. 205-209
Author(s):  
P. A. Novikov ◽  
A. V. Kuz'mich ◽  
L. A. Sergeeva
Keyword(s):  
Phase Transition ◽  
Porous Materials ◽  
Salt Solution ◽  
Aqueous Salt Solution

Transmembrane potential in vesicles formed by catanionic surfactant mixtures in an aqueous salt solution

2020 ◽  
Vol 22 (45) ◽  
pp. 26438-26451
Author(s):  
Ksenia A. Emelyanova ◽  
Polina O. Sorina ◽  
Alexey I. Victorov
Keyword(s):  
Salt Solution ◽  
Transmembrane Potential ◽  
Aqueous Salt Solution ◽  
Simple Theory ◽  
Surfactant Mixtures ◽  
Catanionic Surfactant

Simple theory shows the effects of vesicle structure and the composition of the medium on the transmembrane potential.

Spectrophotometry Study of Aqueous Salt Solution in Carbon Dioxide Microemulsions

Langmuir ◽  
2002 ◽  
Vol 18 (10) ◽  
pp. 3787-3791 ◽  
Author(s):  
Mohammed J. Meziani ◽  
Ya-Ping Sun
Keyword(s):  
Carbon Dioxide ◽  
Salt Solution ◽  
Aqueous Salt Solution

scholarly journals Droplet desorption modes at high heat flux

2019 ◽  
Vol 196 ◽  
pp. 00002
Author(s):  
Sergey Misyura ◽  
Anton Meleshkin
Keyword(s):  
Temperature Field ◽  
Salt Solution ◽  
Ambient Air ◽  
Nucleate Boiling ◽  
High Heat ◽  
Droplet Surface ◽  
Aqueous Salt Solution ◽  
Heated Wall ◽  
High Heat Flux ◽  
Desorption Rate

Nonisothermal droplet desorption of aqueous salt solution H2O/LiBr during nucleate boiling was studied experimentally. A droplet was placed on a horizontal heated wall. The initial concentration of salt C0 = 25 %. The wall temperature Tw = 120 °C and ambient air pressure is 1 bar. Thermal images of the temperature field on the droplet surface show an extremely non-uniform temperature field. At nucleate boiling in LiBr salt solution it is incorrect to predict the desorption behavior in stationary approximation. It was previously believed that the rate of evaporation does not vary with time. For the first time it is shown that the desorption rate is divided into several characteristic time intervals. These intervals is characterized by a significant change in the desorption rate.

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