Effect of UV aging on the tensile and fracture mechanical response of syndiotactic polypropylenes of various crystallinity

Syndiotactic polypropylene (sPP) sheets of various crystallinities were subjected to accelerated ultraviolet (UV) aging. The chemical modification of the polymer was followed by FTIR spectroscopy measuring the carbonyl index in transmittance (film) and diffuse reflectance (powder) modes. Both the tensile stress and strain, suitable indicators of the UV aging, changed linearly with the carbonyl index in semilogarithmic representation. The essential work of fracture (EWF) method proved to be less suitable for characterization, as the UV irradiation resulted in surface embrittlement of the polymer. This caused brittle fracture of the notched specimens instead of the required ductile one. On the other hand, the term of the specific work of fracture related to yielding may adequately reflect the structural and morphological changes of sPP caused by UV irradiation. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3462–3469, 2004     

Toughened carbon fiber fabric‐reinforced pCBT composites

Toughened carbon fiber‐fabric reinforced polymerized cyclic butylene terephthalate (pCBT) composites were obtained by chemical modification of cyclic butylene terephthalate (CBT) with small amounts of epoxy resin and isocyanates as chain extenders. Homogeneous CBT/epoxy and CBT/isocyanate blends were prepared by melt blending the components in a lab‐scale batch mixer at low temperatures and high shear rate. Melt blending was stopped before the ring‐opening polymerization of CBT could start. The modified CBT was the starting material for carbon fiber fabric‐reinforced pCBT composites (fiber content at about 65 wt%) which were prepared by ring‐opening polymerization during compression molding using a simple powder prepreg method. Interlaminar shear strength, flexural strength, and failure strain of the chemically modified composites increased up to 60% with respect to unmodified pCBT composites. Nevertheless, the flexural moduli slightly decreased due to the toughening effect of the chain extender on the pCBT matrix. Drop weight impact tests revealed that the energy absorption of the modified composites was relatively higher as compared to unmodified pCBT composites. POLYM. COMPOS., 37:1453–1460, 2016. © 2014 Society of Plastics Engineers     

Effect of modified layered silicates on the confined crystalline morphology and thermomechanical properties of poly(ethylene oxide) nanocomposites

In this work, poly(ethylene oxide) (PEO)/organoclay nanocomposites with three different types of nanoclays (Cloisite 30B, Somasif JAD400, and Somasif JAD230) were prepared by melt mixing with a laboratory kneader followed by compression molding. The nanocomposites were characterized by atomic force microscopy and scanning electron microscopy. Their crystallization behavior on a hot stage was investigated with polarized optical microscopy. The size and regularity of the spherulites of the PEO matrix were altered significantly by the incorporation of Cloisite 30B, but there was not as much variation with the other two clays. The dynamic viscoelastic behavior of the PEO/organoclay nanocomposites was assessed with a strain‐controlled parallel‐plate rheometer. The effects of clay modification on the thermomechanical and rheological properties were addressed. The reinforcing effect of the organoclay was determined with dynamic mechanical analysis and tensile testing. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Preparation and characterization of polypropylene homocomposites: Exploiting polymorphism of PP homopolymer

In this study, the properties of polypropylene (PP) homocomposites, prepared by film‐stacking followed by hot pressing, were investigated. Alpha‐ and beta‐PP served as matrices, whereas highly oriented PP tapes of the alpha form acted as reinforcement in the homocomposites. Tapes with different draw ratios (DR = 6–12) have been produced and characterized by mechanical and wide‐angle X‐ray scattering measurements. Tapes with a DR = 8 were incorporated in a cross‐ply (CP) manner in the corresponding homocomposite laminates. Specimens were subjected to static (tensile, flexural) and dynamic (instrumented falling weight impact, IFWI) tests. The thermal and thermomechanical properties of the PP tapes and homocomposites were studied by differential scanning calorimetry and dynamic mechanical thermal analysis. The homocomposite morphology was probed by polarized light microscopy, which gave evidence of transcrystalline layer at the interface between tape and matrix. The storage modulus of the CP homocomposites was improved prominently by the tape reinforcement. In static tensile tests, the homocomposites exhibited much higher stiffness and strength when compared with the neat PP specimens. However, this was accompanied with a marked reduction in the ultimate elongation. The IFWI tests showed that both alpha‐ and the beta‐PP failed in macroscopically brittle manner, whereas the corresponding homocomposites failed in semiductile way. The homocomposite laminates prepared with beta‐PP matrix exhibited higher resistance to penetration than those with alpha‐PP. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Interactions and Chemical Transformations of Coronene Inside and Outside Carbon Nanotubes

By exposing flat and curved carbon surfaces to coronene, a variety of van der Waals hybrid heterostructures are prepared, including coronene encapsulated in carbon nanotubes, and coronene and dicoronylene adsorbed on nanotubes or graphite via π–π interactions. The structure of the final product is determined by the temperature of the experiment and the curvature of the carbon surface. While at temperatures below and close to the sublimation point of coronene, nanotubes with suitable diameters are filled with single coronene molecules, at higher temperatures additional dimerization and oligomerization of coronene occurs on the surface of carbon nanotubes. The fact that dicoronylene and possible higher oligomers are formed at lower temperatures than expected for vapor‐phase polymerization indicates the active role of the carbon surface used primarily as template. Removal of adsorbed species from the nanotube surface is of utmost importance for reliable characterization of encapsulated molecules: it is demonstrated that the green fluorescence attributed previously to encapsulated coronene is instead caused by dicoronylene adsorbed on the surface which can be solubilized and removed using surfactants. After removing most of the adsorbed layer, a combination of Raman spectroscopy and transmission electron microscopy was employed to follow the transformation dynamics of coronene molecules inside nanotubes.     

Two-phase solvent extraction of canola

The equilibrium relationships in the extraction process that was developed in our research laboratory for the treatment of canola were studied. In the process, hexane is used as well as CH₃OH that contains 5% (vol/vol) H₂O and 0.08% (w/w) NaOH to simultaneously produce improved meal and high-quality oil. Equilibrium data for canola oil in the hexane-CH₃OH/H₂o/NaOH, meal-hexane, and meal-CH₃OH/H₂O/NaOH-hexane systems are reported. A high partition coefficient for oil between hexane and the polar phase provided a large driving force for mass transfer. The presence of the CH₃OH phase improved oil extraction, probably by rupturing the cell structure. The process proved to be a somewhat less desirable replacement for CH₃OH/H₂O/NH₃ extraction and recovered 93.5% of the oil and 91.8% of the protein in the seed, while with CH₃OH/H₂O/NH₃, the oil and protein recoveries were 96.8 and 94.0%, respectively. The NaOH treatment removed only 50.2% of the glucosinolates, and some of the oil was hydrolyzed by the NaOH, making the process less effective, despite its simplicity.     

Stimulating Cooperation in Self-Organizing Mobile Ad Hoc Networks

In military and rescue applications of mobile ad hoc networks, all the nodes belong to the same authority; therefore, they are motivated to cooperate in order to support the basic functions of the network. In this paper, we consider the case when each node is its own authority and tries to maximize the benefits it gets from the network. More precisely, we assume that the nodes are not willing to forward packets for the benefit of other nodes. This problem may arise in civilian applications of mobile ad hoc networks. In order to stimulate the nodes for packet forwarding, we propose a simple mechanism based on a counter in each node. We study the behavior of the proposed mechanism analytically and by means of simulations, and detail the way in which it could be protected against misuse.     

Morphological study on the effect of elastomeric impact modifiers in polypropylene systems

The morphological effect of elastomeric impact modifiers has been studied in polypropylene systems by wide-angle and small-angle X-ray diffractometry, small-angle light scattering, light and electron microscopy and differential scanning calorimetry. It was established that the incorporation of an impact modifier altered the superstructure of the polypropylene matrix by decreasing the average size of spherulites through which the impact strength of the composite may be influenced. The changes in the mechanical and thermal properties are probably caused by the interphase between the amorphous elastomeric modifier and the polypropylene spherulites. The particle size of the dispersed elastomer is of vital importance in toughening of the amorphous polymer while in the crystalline resin, the changes in the superstructure also seem to be very important. Above T_g, the amorphous impact modifier acts as an energy absorber which markedly influences the crazing susceptibility of the polypropylene matrix.