Topic
Miscibility
About: Miscibility is a research topic. Over the lifetime, 5521 publications have been published within this topic receiving 133547 citations. The topic is also known as: miscible.
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TL;DR: The purpose of the study was to investigate and identify the interactions within solid dispersions of cationic drugs and anionic polymers processed by hot-melt extrusion (HME) technique and found intermolecular ionic interactions varied according to the drug-polymer miscibility.
134 citations
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TL;DR: Etude theorique de la relation temperature de transition vitreuse-composition des melanges de polycaprolactone/polymere chlore as discussed by the authors, et al.
Abstract: Etude theorique de la relation temperature de transition vitreuse-composition des melanges de polycaprolactone/polymere chlore
133 citations
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TL;DR: In this paper, the interaction energies of low molecular weight polymers were calculated by fitting spinodal curves predicted by the Flory-Huggins theory and the Sanchez-Lacombe equation of state theory to experimental cloud point data.
Abstract: Interaction energies for each of the binary pairs PS/Pα-MS, PS/PMMA, and PMMA/Pα-MS were calculated by fitting spinodal curves predicted by the Flory-Huggins theory and the Sanchez-Lacombe equation of state theory to experimental cloud point data for blends of low molecular weight polymers. For blends of PS and Pα-MS, where cloud points could not be observed, the molecular weight limit of miscibility was used to bracket the interaction energy. Phase separation boundaries for this system were predicted to be caused by UCST-type behavior. Oligomeric blends of PMMA with PS showed UCST-type phase boundaries while blends of PMMA with Pα-MS showed LCST-type boundaries. The mechanism of phase separation boundaries was found to stem from the differences between the characteristic temperatures for the pure components (ΔT * )
132 citations
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TL;DR: The phase equilibrium in C8H17(OCH2CH2)3OH/water/decane system was studied at 13.6, 15.8, 21.5, 26.0, and 30.0 °C.
Abstract: The phase equilibrium in C8H17(OCH2CH2)3OH/water/decane system was studied at 13.6, 15.8, 21.5, 26.0, and 30.0 °C. An upper critical solution point for the surfactant and oil phases, and a lower critical solution point for the surfactant and water phases were found. Strong critical opalescence was observed in the vicinity of the critical points. In a temperature range between two critical points, a three-phase region appeared due to the superposition of three miscibility gaps, i.e., 1) surfactant+water; 2) surfactant+oil, and 3) oil+water phases. The correlations between the phase equilibria and the ultralow interfacial tensions were straightforward. An ionic surfactant/cosurfactant/brine/oil system gave similar phase equilibria as the nonionic surfactant system, but the effect of temperature was the reverse.
131 citations
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TL;DR: In this article, it was shown that random copolymers of methyl methacrylate (MMA) and N,N-dimethylacrylamide (DMA) containing different molar fractions of DMA can be used as a miscible block for the nanostructuration of epoxies, a fact that is particularly illustrated for a DGEBA−DDS epoxy network.
Abstract: Nanostructured thermosets may be obtained by the self-assembly of amphiphilic block copolymers (BCP) in a reactive solvent and fixation of the resulting morphologies by the cross-linking reaction. Nanostructuration requires the presence of a block that remains miscible in the thermosetting polymer during polymerization. The selection of the miscible block depends on the particular system, and in some cases (e.g., for epoxy−amine network based on diglycidyl ether of bisphenol A, DGEBA, and 4,4‘-diaminodiphenyl sulfone, DDS) it is very difficult to find such a block. In this paper it is shown that random copolymers of methyl methacrylate (MMA) and N,N-dimethylacrylamide (DMA) containing different molar fractions of DMA can be used as a miscible block for the nanostructuration of epoxies, a fact that is particularly illustrated for a DGEBA−DDS epoxy network. The miscibility of the random copolymer during formation of the epoxy network was first analyzed determining cloud-point conversions as a function of th...
131 citations