scholarly journals Dynamics and growth of droplets close to the two-phase coexistence curve in fluids

Soft Matter ◽  
2013 ◽  
Vol 9 (16) ◽  
pp. 4178 ◽  
Author(s):  
Sutapa Roy ◽  
Subir K. Das
1999 ◽  
Vol 111 (14) ◽  
pp. 6617-6624 ◽  
Author(s):  
Mitsuo Nakata ◽  
Toshiaki Dobashi ◽  
Yu-ichi Inakuma ◽  
Kiyotaka Yamamura

2014 ◽  
Vol 136 (49) ◽  
pp. 16962-16965 ◽  
Author(s):  
Seyed R. Tabaei ◽  
Joshua A. Jackman ◽  
Bo Liedberg ◽  
Atul N. Parikh ◽  
Nam-Joon Cho

2009 ◽  
Vol 92 (7) ◽  
pp. 1552-1555 ◽  
Author(s):  
Yaodong Yang ◽  
Shashank Priya ◽  
Jie-Fang Li ◽  
Dwight Viehland

The study of phase equilibria is historically one of the most important sources of information about the nature of intermolecular forces in non-electrolyte liquids and their mixtures. Many of the main features of vapour-liquid and liquid-liquid phase behaviour were already well characterized experimentally during the early part of this century, but the theoretical explanation of phase equilibria for a wide variety of substances and over a large range of pressures and temperatures has lagged far behind. This paper presents theoretical studies of phase equilibria in binary mixtures obeying the van der Waals equation, especially liquid-liquid equilibria that can occur at high pressures. The variety of fluid phase behaviour that occurs in binary mixtures can be qualitatively discussed in terms of the changes in thermodynamic properties near critical points. Upper critical solution temperatures (UCSTs) occur when a heterogeneous (two-phase) system becomes a homogeneous (one-phase) system when the temperature is raised. The maximum temperature along the temperature-mole fraction ( T, x ) coexistence curve for constant pressure is the UCST at this pressure. Lower critical solution temperatures (LCSTs) occur when a homogeneous system becomes a two-phase system when the temperature is increased. The LCST is at the minimum of the T, x coexistence curve. Thermodynamic considerations of critical points yield requirements for the curvature of the mixing functions plotted against x .


2020 ◽  
Vol 75 (1) ◽  
pp. 87-93 ◽  
Author(s):  
Sergey V. Adichtchev ◽  
Konstantin A. Okotrub ◽  
Alexey M. Pugachev ◽  
Irina V. Zaytseva ◽  
Nikolay V. Surovtsev

Binary phospholipid bilayers composed of 1,2-dioleoyl-sn-glycero-3-phosphocholine and 1,2-palmitoyl-sn-glycero-3-phosphocholine (DPPC) were studied by Raman spectroscopy and differential scanning calorimetry (DSC). We examined features in Raman scattering spectra that are sensitive to the lipid phase and, therefore, could indicate the phase coexistence. It was found that the low-frequency half-width of half-maximum (LHWHM) of the 2850 cm−1 Raman line, corresponding to the symmetric CH2 stretching vibrations, unequivocally reveals the coexisting phospholipids in ordered and disordered conformational states, which correspond to ordered and disordered phases coexistence, in the DPPC mole concentration range from 0.4 to 0.9. The phase coexistence in this concentration range was supported by the particular concentration behavior of the ratio between the intensities of the 2880 cm−1 antisymmetric CH2 vibration line and the 2850 cm−1 symmetric one. It was also shown that the spectral shape of the 1300 cm−1 Raman line, corresponding to the CH2 twisting vibrations, is a good indicator for the phase state and phase coexistence in the phospholipid bilayers. Comparison with the DSC curves confirmed that in the DPPC mole concentration range from 0.4 to 0.9, the two phase transition peaks are observed in DSC curve, those positions are independent of the DPPC concentration. The outcome of the study is the robust label-free contactless approach for the detection of the lipid phase separation, which can be realized with the micrometer resolution.


2014 ◽  
Vol 31 (4) ◽  
pp. 1057-1064 ◽  
Author(s):  
A. M. Lopes ◽  
V. C. Santos-Ebinuma ◽  
A. Pessoa Júnior ◽  
C. O. Rangel-Yagui

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