scholarly journals Phase separation dynamics in aqueous solutions of thermoresponsive polymers

2021 ◽  
Vol 24 (4) ◽  
pp. 43601
Author(s):  
V. Kovalchuk

Phase transition kinetics of aqueous hydroxypropyl cellulose solution was studied by using turbidimetric monitoring and mathematical modelling techniques. Based on the nonlinear Cahn-Hilliard equation with a mobility depending on the component concentration, the phase separation has been modeled on a simple one-dimensional Flory lattice. For value set of the interfacial energy parameter, data were obtained on the changing of the average values of the cluster sizes, their mass and concentration. The simulation results allow us to distinguish three stages of the spinodal decomposition: early, intermediate and final. It was found that for the intermediate stage, the kinetics of the cluster mass growth is described by a dependence that is characteristic of the usual diffusion mass transfer; the change in the average cluster size can be represented by a scaling function with an exponent close to 1/3, typical of the systems with a conserved scalar order parameter. It is shown that the concentration of clusters at the final stage is determined by the temperature dependence of the interfacial energy.

2020 ◽  
pp. 129088
Author(s):  
Yael Templeman ◽  
Malki Pinkas ◽  
Eli Brosh ◽  
Einat Strumza ◽  
Shmuel Hayun ◽  
...  

1995 ◽  
Vol 398 ◽  
Author(s):  
Joshua W. Kriesel ◽  
Susanne M. Lee

ABSTRACTUsing rf sputtering and post-deposition annealing in a differential scanning calorimeter (DSC), we manufactured bulk (4000 nm) films of crystalline Ge0.83Sn0.17. This Sn concentration is much greater than the solid solubility limit of Sn in Ge (x ≤ 0.01). Continued annealing thermally induces Sn phase separation from the alloy, limiting the ultimate attainable grain size in the metastable crystals. We examine, here, the mechanisms and kinetics of the processes limiting the size of the Ge0.83Sn0.17 polycrystals. From a combination of DSC, electron microprobe, and x-ray diffraction (XRD) measurements, we propose phase transformation mechanisms corresponding to crystallization of amorphous Ge0.83Sn0.17, crystallization of an as-yet unidentified phase of Sn, and phase separation of Sn from the Ge1-xSnx crystals. We were unable to observe the unidentified phase of Sn in XRD, but the phase must be present in the material to account for the quantitative discrepancies (as much as 8 at.%) in Sn percentages determined from each of the DSC, XRD, and electron microprobe measurements. Our models for the various transformation kinetics were corroborated by the subsequent phase-separated Sn melting behavior observed in the DSC: two Sn melting endotherms, one of which was 20–100°C lower than the bulk melting temperature of Sn. This depressed temperature endotherm we speculate represents liquefaction of nanometer-sized (β–Sn clusters.


2021 ◽  
Vol 120 (7) ◽  
pp. 1219-1230 ◽  
Author(s):  
Jerelle A. Joseph ◽  
Jorge R. Espinosa ◽  
Ignacio Sanchez-Burgos ◽  
Adiran Garaizar ◽  
Daan Frenkel ◽  
...  

1999 ◽  
Vol 60 (2) ◽  
pp. 822-830 ◽  
Author(s):  
S. Mazumder ◽  
D. Sen ◽  
I. S. Batra ◽  
R. Tewari ◽  
G. K. Dey ◽  
...  

2005 ◽  
Vol 67 (1) ◽  
pp. 85-96 ◽  
Author(s):  
V. V. Slezov ◽  
A. S. Abyzov ◽  
Zh. V. Slezova

2009 ◽  
Vol 113 (26) ◽  
pp. 8820-8827 ◽  
Author(s):  
Yanhua Niu ◽  
Liang Yang ◽  
Katsumi Shimizu ◽  
Jai A. Pathak ◽  
Howard Wang ◽  
...  

2005 ◽  
Vol 138 (3-4) ◽  
pp. 823-828
Author(s):  
N. Mikhin ◽  
V. Grigor’ev ◽  
V. Maidanov ◽  
A. Penzev ◽  
S. Rubets ◽  
...  

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