A phase field model for dynamic simulations of reactive blending of polymers

A facile way to generate compatibilized blends of immiscible polymers is through reactive blending of end-functionalized homopolymers. The reaction may be reversible or irreversible depending on the end-groups and is...

Melt Spinning of Flexible and Conductive Immiscible Thermoplastic/Elastomer Monofilament for Water Detection

In many textile fields, such as industrial structures or clothes, one way to detect a specific liquid leak is the electrical conductivity variation of a yarn. This yarn can be developed using melt spun of Conductive Polymer Composites (CPCs), which blend insulating polymer and electrically conductive fillers. This study examines the influence of the proportions of an immiscible thermoplastic/elastomer blend for its implementation and its water detection. The thermoplastic polymer used for the detection property is the polyamide 6.6 (PA6.6) filled with enough carbon nanotubes (CNT) to exceed the percolation threshold. However, the addition of fillers decreases the polymer fluidity, resulting in the difficulty to implement the CPC. Using an immiscible polymers blend with an elastomer, which is a propylene-based elastomer (PBE) permits to increase this fluidity and to create a flexible conductive monofilament. After characterizations (morphology, rheological and mechanical) of this blend (PA6.6CNT/PBE) in different proportions, two principles of water detection are established and carried out with the monofilaments: the principle of absorption and the short circuit. It is found that the morphology of the immiscible polymer blend had a significant role in the water detection.

Morphology optimization of poly(ethylene terephthalate)/polyamide blends compatibilized via extension-dominated twin-screw extrusion

Poly(ethylene terephthalate) (PET) and polyamide (PA) are immiscible polymers, which requires the use of compatibilizers to stabilize the morphology and achieve acceptable property levels. Therefore, controlling the degree of dispersion, especially the size of the disperse PA droplets in the PET matrix is of paramount importance. This study aims to improve the mixing, i.e., minimize PA droplet size, in immiscible and compatibilized PET/PA and PET/Nylon-MXD6 (MXD6) blends by resorting to extension-dominated mixing in twin-screw extrusion (TSE). MXD6 is an aromatic polyamide similar in polarity to PET, so it is expected that it will blend more effectively than is the case with aliphatic nylon-6 and PET. Two screw configurations are used, a benchmark shear-dominated screw with kneading blocks (KBs) in an aggressive configuration, and an extension-dominated screw configuration with static mixers with hyperbolic C–D channels, recently developed by our group, in place of the KBs. The results show that the use of extensional mixing elements (EMEs) in place of KBs results in a significant decrease of both average and maximum droplet size for all blends, and up to more than one order of magnitude between the most extreme cases of the KB-processed immiscible blend and EME-processed compatibilized blends.

Microstructural Evolution of Poly(ε-Caprolactone), Its Immiscible Blend, and In Situ Generated Nanocomposites

Polymer–polymer systems with special phase morphology were prepared, leading to an exceptional combination of strength, modulus, and ductility. Two immiscible polymers: poly(ε-caprolactone) (PCL) and polyhydroxyalkanoate (PHA) were used as components for manufacturing a nanoblend and a nanocomposite characterized by nanodroplet-matrix and nanofibril-matrix morphologies, respectively. Nanofibrils were formed by high shear of nanodroplets at sufficiently low temperature to stabilize their fibrillar shape by shear-induced crystallization. The effects of nanodroplet vs. nanofiber morphology on the tensile mechanical behavior of the nanocomposites were elucidated with the help of in situ 2D small-angle X-ray scattering, microcalorimetry and 2D wide-angle X-ray diffraction. For neat PCL and a PCL/PHA blend, the evolution of the structure under uniaxial tension was accompanied by extensive fragmentation of crystalline lamellae with the onset at strain e = 0.1. Limited lamellae fragmentation in the PCL/PHA composite occurred continuously over a wide range of deformations (e = 0.1–1.1) and facilitated plastic flow of the composite and was associated with the presence of a PHA nanofiber network that transferred local stress to the PCL lamellae, enforcing their local deformation. The PHA nanofibers acted as crystallization nuclei for PCL during their strain-induced melting–recrystallization.

PLA/PHB Blends: Biocompatibilizer Effects

The purpose of this work was to formulate a fully bio-based blend with superior properties, based on two immiscible polymers: polylactic acid (PLA) and poly-hydroxy butyrate (PHB). To improve the miscibility between the polymeric phases, two different kinds of compatibilizers with a different chemical structure were used, namely, an ethylene oxide/propylene oxide block copolymer in the form of flakes and a mixture of two liquid surfactants with a variable lipophilic–hydrophilic index. The morphology of the blends and their thermal, mechanical, and rheological behavior were evaluated, aiming at assessing the influence of the selected compatibilizers on the microstructure and final properties of the systems. Morphological analyses of the compatibilized blends indicated that the liquid surfactant is more effective than the solid copolymer in inducing morphology refinement, as also suggested by results coming from rheological measurements. Furthermore, thermal analyses demonstrated that the presence of both kinds of compatibilizers induced an enhancement of the crystallinity content of blends. Finally, a remarkable increase of the elastic modulus values was obtained for the compatibilized blends as compared to the pure counterparts, with a consequent significant enhancement of the HDT values.

Electrospun acellular scaffolds for mimicking the natural anisotropy of the extracellular matrix

Co-axial electrospinning of three immiscible polymers by sequentially blending in solvents of different boiling points to obtain biomimetic scaffolds.

Permeation of Toluene into (Polypropylene/Acrylonitrile-co-butadiene Rubber) immiscible blend

This study examines the unsteady permeation process of a solvent through a mixture of two immiscible polymers with a complex dividing interface. The mathematical model consists of three nonlinear PDEs that incorporate the coupling arising between mass transport and the dynamic changes of the blend internal structure. In addition to the solvent mass fraction c, we choose, as additional state variables, the conformation tensor m to characterize the macromolecular chains while the embedded interface is described by a scalar Q and a traceless second-order tensor q respectively for the size and shape anisotropy of the area. We extend the Fick's first law by two new non-Fickian terms. Among the obtained results, we present the transient permeation mass flux profiles of toluene through PP/NBR blend system at different compositions and predict the corresponding time lag.