Cellular polypropylene‐based piezoelectric films

Cellular polypropylene‐calcium carbonate based piezoelectric films were obtained using biaxial stretching and gas‐mediated inflation followed by a corona discharge treatment using home‐made devices. The obtained results revealed a cellular structure that develops at the interface between the solid particles and the polymer matrix and the final piezoelectric coefficient was found to depend both on the gas pressure profile and on time. The inflation step gives better results when the gas pressure is increased in stepwise manner allowing the gas to adequately intrude the cavities and maintain the required pressure. The overall results are discussed in terms of processing conditions and in terms of the developed microstructure. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Morphology Development in Novel Composition of Thermoplastic Vulcanizates Based on PA12/PDMS Reactive Blends

The main objective of the present work was to tailor a new thermoplastic vulcanisate (TPV) composed of PA 12 as the thermoplastic phase and PDMS as the rubber phase. The PDMS was crosslinked by dicumyl peroxide (DCP). Interestingly, addition of 2,2,6,6‐tetramethylpiperidinyloxyl (TEMPO) to the TPV provided the compatibilization of the PA12/PDMS blend in the dynamic process and gave a new material with control structure and morphology. The electron microscopy (SEM and TEM) studies revealed that adding silica nanoparticles and Lotader in PA12 and PDMS phases, respectively, led to a drastic reduction in R_v of the PDMS particles from 16.5 µm (virgin blend) to nearly 0.6 µm for the PA12/PDMS reactive blend. Therefore, a stable co‐continuous morphology was obtained for the new TPV based on 60–40 wt.‐% of PDMS‐PA12 blend.

     

Cover Picture: Macromol. Mater. Eng. 8/2005

Summary: Poly(butylene succinate‐co‐adipate) (PBSA) and organically modified montmorillonite (OMMT) nanocomposites of three different compositions were prepared by melt‐extrusion in a batch mixer. The structure of the nanocomposites was studied using X‐ray diffraction (XRD) and transmission electron microscopy (TEM) that revealed a coexistence of exfoliated and intercalated silicate layers dispersed in the PBSA matrix, regardless of the silicate loading. The degree of crystallinity of PBSA decreases with the addition of OMMT platelets. Dynamic mechanical analysis revealed remarkable increase in flexural storage modulus when compared with that of neat PBSA. Tensile property measurements exhibit substantial increase in stiffness with simultaneous increase in elongation at break of nanocomposites as compared to that of neat PBSA. The effect of clay loading on the melt‐state linear viscoelastic behavior of mixed intercalated/exfoliated nanocomposites was also investigated.

Elongation at break of compression molded annealed samples of neat PBSA and various PBSACNs.     

Heterogeneous PHPMA hydrogels for tissue repair and axonal regeneration in the injured spinal cord

A biocompatible heterogeneous hydrogel of poly[N-(2-hydroxypropyl) methacrylamide] (PHPMA) showing an open porous structure, viscoelastic properties similar to the neural tissue and a large surface area available for cell interaction, was evaluated for its ability to promote tissue repair and axonal regeneration in the transected rat spinal cord. After implantation, the polymer hydrogel could correctly bridge the tissue defect, from a permissive interface with the host tissue to favour cell ingrowth, angiogenesis and axonal growth occurred within the microstructure of the network. Within 3 months the polymer implant was invaded by host derived tissue, glial cells, blood vessels and axons penetrated the hydrogel implant. Such polymer hydrogel matrices which show neuroinductive and neuroconductive properties have the potential to repair tissue defects in the central nervous system by promoting the formation of a tissue matrix and axonal growth by replacing the lost of tissue.     

Effect of compatibilization on the deformation and breakup of drops in step-wise increasing shear flow

Drop deformation and breakup were investigated in the presence of a block copolymer in step-wise simple shear flow using a home-made Couette cell connected to an Anton Paar MCR500 rheometer. Polyisobutylene (PIB) was used as the matrix, while five different molecular weights of polydimethylsiloxane (PDMS) were selected to provide drops with a relatively wide range of viscosity ratio. A block copolymer made of PDMS-PIB was used for interfacial modification of the drop-matrix system. The copolymer concentration was 2 wt% based on the drop phase. The experiments consisted in analyzing the drop shape and measuring the variation of the length to diameter ratio, L/D, both in steady state and in transient regimes till breakup. This allowed revising of the classical Grace curve that reports the variation of the critical capillary number for breakup as a function of viscosity ratio and providing also a new one for blends compatibilized with an interfacial active agent with a given molecular weight.     

Tensile mechanical properties of sulfonated poly(ether ether ketone) (SPEEK) and BPO4/SPEEK membranes

A study to evaluate the tensile mechanical properties of sulfonated poly(ether ether ketone) (SPEEK) and BPO₄/SPEEK composite membranes has been carried out. It is aimed to give an assessment of these materials for applications in proton exchange membrane fuel cells. The stress–strain response of the membranes was measured as a function of the degree of sulfonation (DS) and the filler–matrix ratio. In addition, the effects of immersion in water at various temperatures were explored in situ by means of a homemade testing chamber fitted to the tensile analyzer. The results indicate that the DS has an important influence on the final mechanical behavior of the membranes. The introduction of the BPO₄ solid filler leads to deterioration in mechanical performance compared to unfilled SPEEK. A general picture of the microstructural features influencing the mechanical properties of SPEEK and BPO₄/SPEEK membranes is proposed. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2380–2393, 2005     

Role of organically modified layered silicate as an active interfacial modifier in immiscible polystyrene/polypropylene blends

The role of organically modified layered silicate as a compatibilizer for immiscible polystyrene (PS) with polypropylene (PP) or polypropylene grafted with maleic anhydride (PP-g-MA) blends was investigated. Scanning electron micrographs (SEM) revealed efficient mixing of the polymers in the presence of organically modified layered silicate. X-ray diffraction (XRD) patterns and transmission electron microscopic (TEM) observations showed that silicate layers were either intercalated or exfoliated, depending on their interactions with the polymer pair, and were located at the interface between the two polymers. The compatibilizing action of the organically modified layered silicate resulted in a decrease in interfacial tension and particle size and in a remarkable increase in mechanical properties of the modified immiscible blends.     

Biaxial stretching of polymers using a novel and versatile stretching system

A novel versatile biaxial stretching module that can be adapted to any uniaxial traction testing machine was developed to generate consecutive or simultaneous two‐directional biaxial stretching at various stretching ratios and draw rates. The module allows direct conversion of the uniaxial machine displacement to transverse displacement with a precise adjustment of the stretch ratio between the transverse of the longitudinal strains. Additionally, the developed device allows simultaneous measurements of films mechanical properties in the two directions. The efficiency and the accuracy of the module were verified without and with standard polymer films such as polypropylene and high density polyethylene. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers