Our continuing study of the mechanism of flammability reduction of polymer−layered-silicate nanocomposites has yielded results for polypropylene-graft-maleic anhydride and
polystyrene−layered-silicate nanocomposites using montmorillonite and fluorohectorite. Cone
calorimetry was used to measure the heat release rate and other flammability properties of
the nanocomposites, under well-controlled combustion conditions. Both the polymer−layered-silicate nanocomposites and the combustion residues were studied by transmission electron
microscopy and X-ray diffraction. We have found evidence for a common mechanism of
flammability reduction. We also found that the type of layered silicate, nanodispersion, and
processing degradation have an influence on the flammability reduction.
The solid–liquid phase transition temperatures and heats of fusion ΔHf of nonpolar organic solids confined in the pores of controlled pore glasses were measured by differential scanning calorimetry. The pore diameters d were in the range of 40–730 Å and the organics studied were cis-decalin, trans-decalin, cyclohexane, benzene, chlorobenzene, naphthalene, and heptane. In accordance with previous reports on studies of primarily inorganic materials, the melting point of the pore solid T(d) decreased with decreasing pore diameter. In addition, a large reduction in the bulk enthalpy of fusion ΔHf of the pore solid was measured, which apparently has not been studied in detail by other workers. A linear correlation was found between the melting point depression (ΔTm) and the reciprocal diameter, as predicted by theories of solidification in a capillary. The calculated values of the solid–liquid interfacial energy σsl were in reasonable agreement with values reported in the literature based on other methods of measurement.
Charged poly(amidoamine) (PAMAM) dendrimers are used to create organic-inorganic hybrid colloids in aqueous solution. The formation of gold colloids upon reduction of a gold salt precursor serves as a model reaction to study the influence of reaction conditions and dendrimer generation on the resulting nanostructures. Characterization by transmission electron microscopy (TEM), small-angle neutron scattering (SANS), and small-angle X-ray scattering (SAXS) show that the gold particles are formed inside the dendrimer and located offset from the center. Although lower generation dendrimers aggregate when stabilizing the metal particles formed, dendrimers of generation 6-9 can template one gold colloid per dendrimer molecule, the size of which is well-controlled by the number of gold atoms added per dendrimer. For generation 10, multiple smaller gold particles per dendrimer are observed. The effectiveness of PAMAM dendrimers as templates in the host-guest nanoscale synthesis is confirmed for different chemical reactions.
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