“Dynamics of Phase Segrewation in Poly-P-Phenylene Terephtualamide and Amorphous Nylon Molfcular Composites”

1989 ◽  
Vol 171 ◽  
Author(s):  
Thein Kyu ◽  
Jan Chang Yang ◽  
Tsuey Ing Chen
Keyword(s):  
Temperature Jump ◽  
Phase Segregation ◽  
Solution Temperature ◽  
Distilled Water ◽  
Two Phase ◽  
Time Resolved ◽  
Critical Solution Temperature ◽  
Dynamical Scaling ◽  
Molecular Composites ◽  
Phase Temperature

ABSTRACTTime-resolved light scattering has been employed to elucidate the dynamics of phase segregation of poly-p-phenylene terephthalamide (PPTA)/ amorphous nylon (AN) molecular composites. Miscible PPTA/AN blends can be prepared from sulfuric acid solution by rapidly coagulating the solution in distilled water. The composites, however, undergo phase segregation upon thermal treatment and exhibit a miscibility window reminiscent of a lower critical solution temperature (LCST). Several temperature-jump experiments were undertaken from ambient to a two-phase temperature region of 240, 250 and 260°C. Time-evolution of scattering profiles are analyzed in accordance with non-linear and dynamical scaling theories.

Phase Separation Dynamics of Blends of Telechelic Epoxy Terminated Polybutadiene and Maltene

1995 ◽  
Vol 68 (1) ◽  
pp. 158-166 ◽  
Author(s):  
Tsunehiro Yamamoto ◽  
Thein Kyu
Keyword(s):  
Phase Separation ◽  
Scaling Laws ◽  
Phase Region ◽  
Solution Temperature ◽  
Two Phase ◽  
Time Resolved ◽  
Thermally Induced ◽  
Dynamical Scaling ◽  
Upper Critical Solution Temperature ◽  
Deep Temperature

Abstract Thermally induced phase separation in a mixture of telechelic epoxy terminated polybutadiene (ETPB) and maltene has been studied by means of time-resolved light scattering and optical microscopy. Maltene, consisting of various hydrocarbon derivatives, was extracted from asphalt with n-heptane and isolated by centrifugation. The cloud point studies of the ETPB/maltene mixture showed an upper critical solution temperature (UCST) which is thermally reversible. Several deep temperature quench experiments were conducted at an off-critical composition (27/73 ETPB/maltene) from a single phase (80°C) to a two-phase region (27, 29, 31 and 33 °C). The time-evolution of the structure factor for the late stage of spinodal decomposition (SD) was analyzed in the framework of nonlinear and dynamical scaling laws. The reverse quench experiments were also undertaken to elucidate the phase dissolution process.

The Effect of Molecular Architecture on the Phase Diagram and Mobility of a Polymer Blend Exhibiting a Lower Critical Solution Temperature: Cycles Mixed with Linear Chains.

1991 ◽  
Vol 248 ◽  
Author(s):  
Maria M. Santore ◽  
Gregory McKenna ◽  
Charles Han
Keyword(s):  
Phase Diagram ◽  
Phase Separation ◽  
Lower Critical Solution Temperature ◽  
Phase Region ◽  
Solution Temperature ◽  
Free Energy Function ◽  
Molecular Architecture ◽  
Two Phase ◽  
Critical Solution Temperature ◽  
Linear Chains

AbstractWe examine the role of molecular architecture on the phase diagram of the PS/PVME (poly[styrenel /poly[vinyl methyl ether]) blend, a mixture which in previous studies with linear chains exhibited a lower critical solution temperature, (LCST) i.e. it phase separated on heating. In this investigation, two blends with components exceeding the critical molecular weight for entanglement were compared: one consisting of linear PS and PVME and a second with cyclic PS and linear PVME. Cloud point experiments over a broad composition range reveal that the blend containing cyclic PS undergoes phase separation at temperatures 7-8 °C higher than the analogous linear blend. In other words, the mixture of cycles and linear chains is more thermodynamically stable than the mixture of two linear chains.The LCST nature of the system facilitates examining chain mobility by considering the phase separation kinetics. Time-resolved light scattering studies of blends near their critical compositions tracked the spinodal decomposition following a rapid temperature jump from the one-phase to the two-phase region. An analysis of the scattering intensity growth ultimately led to mutual diffusion coefficients whose temperature dependence confirmed the observed cloud points. An approximation of the second derivative of the free energy function based on SANS studies of the linear PS/PVME blend allowed us to estimate mutual mobilities. The values determined for the cycle-containing blend were considerably lower than those for the blend of linear chains at these molecular weights.

Selective Hydrogen Bonding Controls Temperature Response of Layer-by-Layer Upper Critical Solution Temperature Micellar Assemblies

Soft Matter ◽  
2021 ◽  
Author(s):  
Aliaksei Aliakseyeu ◽  
Victoria Albright ◽  
Danielle Yarbrough ◽  
Samantha Hernandez ◽  
Qing Zhou ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Methacrylic Acid ◽  
Temperature Response ◽  
Solution Temperature ◽  
Layer By Layer ◽  
Critical Solution Temperature ◽  
Hydrogen Bonding Interactions ◽  
Upper Critical Solution Temperature ◽  
Lbl Films

This work establishes a correlation between the selectivity of hydrogen-bonding interactions and the functionality of micelle-containing layer-by-layer (LbL) assemblies. Specifically, we explore LbL films formed by assembly of poly(methacrylic acid)...

scholarly journals Thermo- and Photoresponsive Behaviors of Dual-Stimuli-Responsive Organogels Consisting of Homopolymers of Coumarin-Containing Methacrylate

Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 329
Author(s):  
Seidai Okada ◽  
Eriko Sato
Keyword(s):  
Functional Group ◽  
Solution Temperature ◽  
Stimuli Responsive ◽  
Critical Solution Temperature ◽  
Equilibrium Degree ◽  
Stimuli Responsive Polymers ◽  
Responsive Polymers ◽  
Dual Functional ◽  
Wide Range ◽  
Increasing Temperature

Coumarin-containing vinyl homopolymers, such as poly(7-methacryloyloxycoumarin) (P1a) and poly(7-(2′-methacryloyloxyethoxy)coumarin) (P1b), show a lower critical solution temperature (LCST) in chloroform, which can be controlled by the [2 + 2] photochemical cycloaddition of the coumarin moiety, and they are recognized as monofunctional dual-stimuli-responsive polymers. A single functional group of monofunctional dual-stimuli-responsive polymers responds to dual stimuli and can be introduced more uniformly and densely than those of dual-functional dual-stimuli-responsive polymers. In this study, considering a wide range of applications, organogels consisting of P1a and P1b, i.e., P1a-gel and P1b-gel, respectively, were synthesized, and their thermo- and photoresponsive behaviors in chloroform were investigated in detail. P1a-gel and P1b-gel in a swollen state (transparent) exhibited phase separation (turbid) through a temperature jump and reached a shrunken state (transparent), i.e., an equilibrium state, over time. Moreover, the equilibrium degree of swelling decreased non-linearly with increasing temperature. Furthermore, different thermoresponsive sites were photopatterned on the organogel through the photodimerization of the coumarin unit. The organogels consisting of homopolymers of coumarin-containing methacrylate exhibited unique thermo- and photoresponsivities and behaved as monofunctional dual-stimuli-responsive organogels.

scholarly journals Time-resolved PIV measurements of a deflected submerged jet interacting with liquid-gas and liquid-liquid interfaces

2021 ◽  
Author(s):  
Stefan Puttinger ◽  
Mahdi Saeedipour
Keyword(s):  
Liquid Layer ◽  
Large Scale ◽  
Free Surface Flow ◽  
Industrial Applications ◽  
Liquid Pool ◽  
Surface Flow ◽  
Two Phase ◽  
Time Resolved ◽  
Submerged Jet ◽  
Major Interest

AbstractThis paper presents an experimental investigation on the interactions of a deflected submerged jet into a liquid pool with its above interface in the absence and presence of an additional lighter liquid. Whereas the former is a free surface flow, the latter mimics a situation of two stratified liquids where the liquid-liquid interface is disturbed by large-scale motions in the liquid pool. Such configurations are encountered in various industrial applications and, in most cases, it is of major interest to avoid the entrainment of droplets from the lighter liquid into the main flow. Therefore, it is important to understand the fluid dynamics in such configurations and to analyze the differences between the cases with and without the additional liquid layer. To study this problem, we applied time-resolved particle image velocimetry experiments with high spatial resolution. A detailed data analysis of a small layer beneath the interface shows that although the presence of an additional liquid layer stabilizes the oscillations of the submerged jet significantly, the amount of kinetic energy, enstrophy, and velocity fluctuations concentrated in the proximity of the interface is higher when the oil layer is present. In addition, we analyze the energy distribution across the eigenmodes of a proper orthogonal distribution and the distribution of strain and vortex dominated regions. As the main objective of this study, these high-resolution time-resolved experimental data provide a validation platform for the development of new models in the context of the volume of fluid-based large eddy simulation of turbulent two-phase flows.

scholarly journals Synthesis of a thermoresponsive crosslinked MEO2MA polymer coating on microclusters of iron oxide nanoparticles

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Alejandro Lapresta-Fernández ◽  
Alfonso Salinas-Castillo ◽  
Luis Fermín Capitán-Vallvey
Keyword(s):  
Iron Oxide ◽  
Synthesis Temperature ◽  
Water Soluble ◽  
Covalent Attachment ◽  
Solution Temperature ◽  
Tetraethylene Glycol ◽  
Critical Solution Temperature ◽  
Large Size ◽  
Transmission Electron ◽  
Azo Initiator

AbstractEncapsulation of magnetic nanoparticles (MNPs) of iron (II, III) oxide (Fe3O4) with a thermopolymeric shell of a crosslinked poly(2-(2-methoxyethoxy)ethyl methacrylate) P(MEO2MA) is successfully developed. Magnetic aggregates of large size, around 150–200 nm are obtained during the functionalization of the iron oxide NPs with vinyl groups by using 3-butenoic acid in the presence of a water soluble azo-initiator and a surfactant, at 70 °C. These polymerizable groups provide a covalent attachment of the P(MEO2MA) shell on the surface of the MNPs while a crosslinked network is achieved by including tetraethylene glycol dimethacrylate in the precipitation polymerization synthesis. Temperature control is used to modulate the swelling-to-collapse transition volume until a maximum of around 21:1 ratio between the expanded: shrunk states (from 364 to 144 nm in diameter) between 9 and 49 °C. The hybrid Fe3O4@P(MEO2MA) microgel exhibits a lower critical solution temperature of 21.9 °C below the corresponding value for P(MEO2MA) (bulk, 26 °C). The MEO2MA coating performance in the hybrid microgel is characterized by dynamic light scattering and transmission electron microscopy. The content of preformed MNPs [up to 30.2 (wt%) vs. microgel] was established by thermogravimetric analysis while magnetic properties by vibrating sample magnetometry.

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