Search results for "Miscibility"

Phase diagrams of the system tetrahydrofuran/γ-butyrolactone/poly(ether imide) and determination of interaction parameters

1998

Abstract The thermodynamic interactions in the ternary mixture tetrahydrofuran/γ-butyrolactone/poly(ether imide) (THF/γ-BL/PEI) are investigated from 30 to 50°C. This is a membrane-forming system with a high He-selectivity. Cloud point measurements show that the two binary polymer solutions THF/PEI and γ-BL/PEI exhibit miscibility gaps which close towards the centre of the ternary phase diagram where the mixtures become homogeneous (cosolvency). Vapour pressures were determined for the subsystem THF/γ-BL. For the theoretical calculations the Gibbs energy of mixing is formulated according to the Flory-Huggins theory and the interaction parameter χ THF γ-BL calculated from the vapour pressure…

Monolayer phases of the fatty acids and their ethyl esters

1991

The miscibility correspondence between water-surface monolayer phases of the fatty acids and their ethyl esters was determined. Ester phases were found corresponding to all the known phases of the acids, and vice versa, in similar relative positions of the π-T diagram. Evidence is presented for the existence of a ninth distinct miscibility category, represented by a phase in each of the pure materials, and a tenth found only in mixtures. We propose a tentative correspondence to bulk smectic miscibility categories.

New binary solid dispersion of indomethacin with surfactant polymer: From physical characterization to in vitro dissolution enhancement

2009

This article investigated preparation of solid dispersions containing a poor water-soluble drug, indomethacin (IND), and a new surfactant polymer, polyoxyethylene 32 distearate (POED). Solid dispersions were prepared by the melting method and characterized by DSC, hot-stage microscopy (HSM), X-ray diffraction (XRD) and scanning electron microscopy (SEM). DSC and HSM analyses performed on IND/POED physical mixtures indicated that IND could dissolve in liquid POED. The materials showed complete miscibility at liquid state. Combination of DSC, XRD, and SEM revealed that these materials had limited miscibility at the solid state. Up to 20% w/w IND in POED, we did not detect significant modifica…

Miscibility and properties of linear poly(l-lactide)/branched poly(l-lactide) copolyester blends

2006

Abstract Polymer blends consisting of linear poly( l -lactide) (PLLA) and different proportions of dendritic PLLA-based copolyesters ( hb -PLLA) characterized by different degrees of branching (DB) were obtained in melt. The solid-state properties of poly( l -lactide)s and their blends were investigated by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), atomic force microscopy (AFM) and stress–strain measurements. DSC and DMA methods proved miscibility of PLLA/ hb -PLLA blends for the studied composition range. AFM indicated that no phase separation occurs in PLLA/ hb -PLLA blends and that PLLA and hb -PLLA cocrystallize in one single lamellae type. The mechanica…

Reactive blending of functionalized acrylic rubbers and epoxy resins

2001

A high molecular weight acrylonitrile/butadiene/methacrylic acid (Nipol 1472) rubber is chosen to control processability and mechanical properties of a TGDDM (tetra glycidyl diphenyl methane) based epoxy resin formulation for aerospace composite applications. The physical blend of rubber and epoxy resin, achieved by dissolution of all the components in a common solvent, forms a heterogeneous system after solvent removal and presents coarse phase separation during cure that impairs any practical relevance of this material. A marked improvement of rubber-epoxy miscibility is achieved by reactive blending ('pre-reaction') the epoxy oligomer with the functional groups present in the rubber. The…

On the structural aspects of solid solutions of enantiomers: an intriguing case study of enantiomer recognition in the solid state

2018

Structural aspects of solid solutions of enantiomers have been considered and the corresponding definitions of type 1 and type 2 solid solutions have been revised based on the available structures reported in the literature. Examples of both types are presented indicating that (e.g., type 1 solid solutions) there is a straightforward relationship between the particular structural aspects and the enantiomer miscibility limits in the solid state. Furthermore, enantiomer recognition in a type 2 solid solution formed by the enantiomers of a pharmaceutically active ingredient, pimobendan, has been studied in more detail. It was found that upon rapid crystallization from a solution a structure po…

Crystal Inclusions in Diamonds and Other Crystals

2013

Single crystal inclusions in natural single crystals bear a lot of information on the genesis and phase stabilities between host and guest crystals. Not only parameters of the natural environment of crystallization may be elucidated, also the history of up-rise within the earth to the surface and the development during procedures, eventually applied by mankind to enhance the physical properties of crystals, may be detectable. Structural reactions resulting in phase separation due to chemical stress during change of physical parameters shed light on the borders of solid solution and exsolution domains. Natural crystals of proper quality allow us to evaluate a time factor in phase stabilities…

Building Bridges by Blending: Morphology and Mechanical Properties of Binary Tapered Diblock/Multiblock Copolymer Blends

2021

Blends of poly(2,6-dimethyl-1,4-phenylene oxide) with styrene copolymers

1994

Binary blends of poly(2,6–dimethyl–1,4–phenylene oxide) (PPE) with various styrene copolymers were investigated. Poly(styrene–co–acrylonitrile) (SAN), poly[styrene–co–(methyl methacrylate)] (SMMA), poly[styrene–co–(acrylic acid)] (SAA) and poly[styrene–co–(maleic anhydride)] (SMA) are only miscible with PPE when the amount of comonomer is rather small. From calculated binary interaction densities it can be concluded that the strong repulsion between PPE and comonomer limits miscibility. In blends of PPE with SAN, as well as with ABS, the inter-facial tension between the blend components is significantly reduced upon addition of polystyrene–block–poly–(methyl methacrylate) diblock copolymers…

Pressure dependence of the demixing of polymer solutions determined by viscometry

1981

From the break-down in the viscosity of a polymer solution, associated with the entrance into the two phase region, the pressure dependence of the demixing temperatures of solutions of polystyrene (M = 600.000) in cyclohexane, cyclopentane, diethylmalonate and 1-phenyldecane was measured up to 1000 bar. The application of pressure increases the solubility of polystyrene in cyclopentane and diethylmalonate, but decreases that in 1-phenyldecane; in the case of cyclohexane, a pressure of optimum miscibility is observed at ca. 120 bar.