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Fluorescence (FL) emission properties, microporous structures, energy-minimized chain conformations, and lamellar layer structures of the silicon-containing poly(diphenylacetylene) derivative of p-PTMSDPA before and after desilylation were investigated. The nitrogen-adsorption isotherms of p-PTMSDPA film before and after desilylation were typical of type I, indicating microporous structures. The BET surface area and pore volume of the p-PTMSDPA film were significantly reduced after the desilylation reaction, simultaneously, its FL emission intensity remarkably decreased. The theoretical calculation on both model compounds of p-PTMSDPA and its desilylated polymer, PDPA, showed a remarkable difference in chain conformation: The side phenyl rings of p-PTMSDPA are discontinuously arranged in a zig-zag pattern, while the PDPA is continuously coiled in a helical manner. The lamellar layer distance (LLD) in the p-PTMSDPA film significantly decreased after the desilylation reaction.

ABSTRACT:The morphology of nylon 6 and polystyrene (PS) blend with styrene-maleic anhydride copolymer (SMA) as a compatibilizing agent was studied. The long-time mixing of blends exhibited slight decrease in storage modulus and larger domain size. This may be caused by imidization between amine end-group of nylon 6, and SMA produce the water, which hydrolyzes an amide group of nylon 6 and results in the decrease of viscosity. As the morphology change in blend influence on physical properties, it is found that modification of nylon 6 by SMA has a better morphology and good physical properties with shorter mixing time.However, the morphology investigation in nylon 6/PS blends reveals that the effect of mixing time was negligibly small. Addition of small amount of SMA into nylon 6/PS blend has proved to give improvement in physical properties. This behavior is based on the concentration of water derived from imidization.

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