Glass transition and alpha-relaxation dynamics of thin films of labeled polystyrene

The glass transition temperature and relaxation dynamics of the segmental motions of thin films of polystyrene labeled with a dye, 4-[N-ethyl-N-(hydroxyethyl)]amino-4-nitraozobenzene (Disperse Red 1, DR1) are investigated using dielectric measurements. The dielectric relaxation strength of the DR1-labeled polystyrene is approximately 65 times larger than that of the unlabeled polystyrene above the glass transition, while there is almost no difference between them below the glass transition. The glass transition temperature of the DR1-labeled polystyrene can be determined as a crossover temperature at which the temperature coefficient of the electric capacitance changes from the value of the glassy state to that of the liquid state. The glass transition temperature of the DR1-labeled polystyrene decreases with decreasing film thickness in a reasonably similar manner to that of the unlabeled polystyrene thin films. The dielectric relaxation spectrum of the DR1-labeled polystyrene is also investigated. As thickness decreases, the $\alpha$-relaxation time becomes smaller and the distribution of the $\alpha$-relaxation times becomes broader. These results show that thin films of DR1-labeled polystyrene are a suitable system for investigating confinement effects of the glass transition dynamics using dielectric relaxation spectroscopy.Comment: 10 pages, 11 figures, 2 Table

Flammability of styrenic polymer clay nanocomposites based on a methyl methacrylate oligomerically-modified clay

Nanocomposites of polystyrene, high impact polystyrene, acrylonitrile–butadiene–styrene terpolymer, polypropylene, and polyethylene were prepared using a methyl methacrylate oligomerically-modified clay by melt blending and the thermal stability and fire retardancy were studied. These nanocomposites were characterized by X-ray diffraction, transmission electron microscopy, thermogravimetric analysis and cone calorimetry. The results show a mixed morphology, depending on the polymer

Structural investigations of poly(ethylene terephthalate)- graft-polystyrene copolymer films

Structural investigations of poly(ethylene terephthalate)-graft-polystyrene (PET-g-PS) films prepared by radiation-induced grafting of styrene onto commercial poly- (ethylene terephthalate) (PET) films were carried out by FTIR, X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The variation in the degree of crystallinity and the thermal characteristics of PETfilms was correlated withthe amount of polystyrene grafted therein (i.e., the degree of grafting). The heat of melting was found to be a function of PET crystalline fraction in the grafted films. The grafting is found to take place by incorporation of amorphous polystyrene grafts in the entire noncrystalline (amorphous) region of the PET films and at the surface of the crystallites. This results in a decrease in the degree of crystallinity with the increase in the degree of grafting, attributed to the dilution of PET crystalline structure with the amorphous polystyrene, without almost any disruption in the inherent crystallinity

Nanocomposites Based on Poly (ε-Caprolactone) (PCL)/Clay Hybrid: Polystyrene, High Impact Polystyrene, ABS, Polypropylene and Polyethylene

Nanocomposites of polystyrene, high impact polystyrene, acrylonitrile–butadiene–styrene terploymer, polypropylene and polyethylene have been prepared using an organically-modified clay that contains polycaprolactone—PCL-modified clay. Depending upon the mode of preparation of the PCL-modified clay, all three types of nanocomposites, immiscible, intercalated and exfoliated, may be produced. The materials have been characterized by X-ray diffraction, transmission electron microscopy, cone calorimetry, thermogravimetric analysis, and the evaluation of mechanical properties

Insecticide-treated nets against malaria vectors and polystyrene beads against Culex larvae.

In Parasitology Today in 1985, Curtis and Lines, and Curtis and Minjas presented the ideas of insecticide-treated nets and polystyrene beads for mosquito control. The former idea has grown to be a major component of the strategy for malaria prevention, especially in Africa. However, although polystyrene beads have been demonstrated to work extremely well, they have yet to be taken up on a major scale

Polystyrene Magadiite Nanocomposites

An organically modified magadiite has been prepared and used to make a mixed intercalated-exfoliated polystyrene nanocomposite by bulk polymerization. This system gives excellent improvement in mechanical properties, but the thermogravimetric analysis curves do not show any change in the onset of the degradation and the degradation pathway is not changed from that for virgin polystyrene, unlike the situation for an aluminosilicate clay, monlmorillonite. By cone calorimetry, the peak heat release rate is not changed, again unlike the results with the aluminosilicate. This suggests that not all clays exhibit the same behavior in nanocomposite formation

Synergistic Effect of Carbon Nanotubes and Decabromodiphenyl Oxide/Sb\u3csub\u3e2\u3c/sub\u3eO\u3csub\u3e3\u3c/sub\u3e in Improving the Flame Retardancy of Polystyrene

Brominated flame retardant polystyrene composites were prepared by melt blending polystyrene, decabromodiphenyl oxide, antimony oxide, multi-wall carbon nanotubes and montmorillonite clay. Synergy between carbon nanotubes and clay and the brominated fire retardant was studied by thermogravimetric analysis, microscale combustion calorimetry and cone calorimetry. Nanotubes are more efficient than clay in improving the flame retardancy of the materials and promoting carbonization in the polystyrene matrix. Comparison of the results from the microscale combustion calorimeter and the cone calorimeter indicate that the rate of change of the peak heat release rate reduction in the microscale combustion calorimeter was slower than that in the cone. Both heat release capacity and reduction in the peak heat release rate in the microscale combustion calorimeter are important for screening the flame retardant materials; they show good correlations with the cone parameters, peak heat release rate and total heat released

Dynamics of Micropollutant Adsorption to Polystyrene Surfaces Probed by Angle-Resolved Second Harmonic Scattering

Angle-resolved second harmonic scattering is used to probe the adsorption dynamics of aqueous cationic and anionic dye molecules onto polystyrene surfaces. The adsorptions of malachite green to negatively charged polystyrene and naphthol yellow S to positively charged polystyrene are both highly favorable, with Î"GAds values of -10.9 ± 0.2 and -10.27 ± 0.09 kcal/mol, respectively. A competitive displacement methodology was employed to obtain values for the adsorption free energies of various smaller neutral organic molecules, including the important micropollutant ascorbic acid, caffeine, and pentoxifylline. For charged adsorbers, electrostatic interactions appear to significantly contribute to adsorption behavior. However, electrostatic repulsion does not necessarily deter the adsorption of molecules with large uncharged moieties (e.g., surfactants). In these cases, the mechanism of adsorption is dominated by van der Waals interactions, with the surface charge playing a relatively minor role

Fire properties of styrenic polymer–clay nanocomposites based on an oligomerically-modified clay

An oligomerically-modified clay has been used to fabricate nanocomposites with styrenic polymers, such as polystyrene, high-impacted polystyrene, poly(styrene-co-acrylonitrile) and acrylonitrile–butadiene–styrene by melt blending. The clay dispersion was evaluated by X-ray diffraction and bright field transmission electron microscopy. All of the nanocomposites have a mixed delaminated/intercalated structure. The fire properties of nanocomposites were evaluated by cone calorimetry and the mechanical properties were also evaluated

Novel Polymerically-Modified Clays Permit the Preparation of Intercalated and Exfoliated Nanocomposites of Styrene and its Copolymers by Melt Blending

Two new organically-modified clays have been made and used to produce nanocomposites of polystyrene, high impact polystyrene and acrylonitrile–butadiene–styrene terploymer. At a minimum, intercalated nanocomposites of all of these polymers have been produced by melt blending in a Brabender mixer and, in some cases, exfoliated nanocomposites have been obtained. The systems have all been characterized by X-ray diffraction, transmission electron microscopy, thermogravimetric analysis, cone calorimetry and the measurement of mechanical properties. These novel new clays open new opportunities for melt blending of polymers with clays to obtain nanocomposites with important properties