Early stages of phase separation from polydisperse polymer mixtures

2001 ◽  
Vol 4 (3) ◽  
pp. 327-336 ◽  
Author(s):  
N. Clarke

1987 ◽  
Vol 20 (7) ◽  
pp. 1671-1681 ◽  
Author(s):  
T. E. Schichtel ◽  
K. Binder


1994 ◽  
Vol 27 (15) ◽  
pp. 4231-4241 ◽  
Author(s):  
C. Huang ◽  
M. Olvera de la Cruz


Minerals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 715
Author(s):  
Miodrag J. Lukić ◽  
Felix Lücke ◽  
Teodora Ilić ◽  
Katharina Petrović ◽  
Denis Gebauer

Nucleation of minerals in the presence of additives is critical for achieving control over the formation of solids in biomineralization processes or during syntheses of advanced hybrid materials. Herein, we investigated the early stages of Fe(III) (oxy)(hydr)oxide formation with/without polyglutamic acid (pGlu) at low driving force for phase separation (pH 2.0 to 3.0). We employed an advanced pH-constant titration assay, X-ray diffraction, thermal analysis with mass spectrometry, Fourier Transform infrared spectroscopy, and scanning electron microscopy. Three stages were observed: initial binding, stabilization of Fe(III) pre-nucleation clusters (PNCs), and phase separation, yielding Fe(III) (oxy)(hydr)oxide. The data suggest that organic–inorganic interactions occurred via binding of olation Fe(III) PNC species. Fourier Transform Infrared Spectroscopy (FTIR) analyses revealed a plausible interaction motif and a conformational adaptation of the polypeptide. The stabilization of the aqueous Fe(III) system against nucleation by pGlu contrasts with the previously reported influence of poly-aspartic acid (pAsp). While this is difficult to explain based on classical nucleation theory, alternative notions such as the so-called PNC pathway provide a possible rationale. Developing a nucleation theory that successfully explains and predicts distinct influences for chemically similar additives like pAsp and pGlu is the Holy Grail toward advancing the knowledge of nucleation, early growth, and structure formation.



2010 ◽  
Vol 81 (8) ◽  
Author(s):  
A. Cornish ◽  
T. Eralp ◽  
A. Shavorskiy ◽  
R. A. Bennett ◽  
G. Held ◽  
...  


Polymers ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 1576
Author(s):  
Biswaroop Mukherjee ◽  
Buddhapriya Chakrabarti

Surface segregation of the low molecular weight component of a polymeric mixture is a ubiquitous phenomenon that leads to degradation of industrial formulations. We report a simultaneous phase separation and surface migration phenomena in oligomer–polymer ( O P ) and oligomer–gel ( O G ) systems following a temperature quench that induces demixing of components. We compute equilibrium and time varying migrant (oligomer) density profiles and wetting layer thickness in these systems using coarse grained molecular dynamics (CGMD) and mesoscale hydrodynamics (MH) simulations. Such multiscale methods quantitatively describe the phenomena over a wide range of length and time scales. We show that surface migration in gel–oligomer systems is significantly reduced on account of network elasticity. Furthermore, the phase separation processes are significantly slowed in gels leading to the modification of the well known Lifshitz–Slyozov–Wagner (LSW) law ℓ ( τ ) ∼ τ 1 / 3 . Our work allows for rational design of polymer/gel–oligomer mixtures with predictable surface segregation characteristics that can be compared against experiments.



2009 ◽  
Vol 79 (10) ◽  
Author(s):  
G. Bonny ◽  
D. Terentyev ◽  
L. Malerba ◽  
D. Van Neck


1988 ◽  
Vol 36 (2) ◽  
pp. 413-424 ◽  
Author(s):  
U.D. Kulkarni ◽  
S. Banerjee




1997 ◽  
Vol 30 (15) ◽  
pp. 4459-4463 ◽  
Author(s):  
N. Clarke ◽  
T. C. B. McLeish ◽  
S. Pavawongsak ◽  
J. S. Higgins


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