缩聚合成聚芳酯和聚酯－聚醚弹性体的微相复合物

通过原位直接缩聚反应，制备了刚性棒状聚对羟基苯甲酸酯（ＰＨＢ）和聚对苯二甲酸丁二醇酯－聚四亚甲基醚多嵌段共聚物（ＰＢＴ－ＰＴＭＧ）的微相复合物．复合物可溶于氯仿等溶剂，可以浇铸成膜．本文研究了ＰＨＢ含量和聚合过程中，基体聚合物溶液浓度对微相复合物形态以及力学性能影响．同共混法相比，原位缩聚法可得到分散更均匀，力学性能更优良的微相复合物．     

Anisotropic dispersion polymerization of N-(4-aminobenzoyl)–caprolactam in polymer melts

When N-(4-aminobenzoyl)–caprolactam (PAC) is injected into polymer melts, dispersions of anisotropic polyaramide particles with average diameters of 100–400 nm and aspect ratios of 5–10 are formed within few minutes. At 200°C PAC dispersion polymerization yields caprolactam and predominantly poly(p-phenylenebenzamide), whereas with increasing polymerization temperatures PAC ring-opening polymerization accounts for the incorporation of 6-aminocaproic acid units into the polyaramide backbone. Covalent bond formation between microparticle surfaces and functional groups of the matrix polymer provides excellent interfacial adhesion and stabilizes the anisotropic polyaramide microparticle dispersions. This in situ PAC dispersion polymerization during melt processing, producing polyaramide-whisker reinforced thermoplastics, represents a versatile route to organic microcomposites exhibiting improved stiffness and strength.     

Tailored flame retardancy via nanofiller dispersion state: Synergistic action between a conventional flame-retardant and nanoclay in high-impact polystyrene

Two preparation techniques attempting to disperse nanoclays in high-impact polystyrene matrix yielded different clay dispersion states either as intercalated or phase-separated morphologies. By this means, the influence of micro- and nanocomposite formation on the synergistic flame retardancy between nanoclays and a conventional mineral-type flame-retardant additive, namely aluminium tri-hydroxide, was investigated in terms of limiting oxygen index, horizontal burning rates and cone calorimetric fire properties. Reductions in peak heat release rates in the cone calorimeter were doubled with nanocomposites relative to microcomposites, attributed to char enhancement and lower mass loss rates. This was accompanied by higher limiting oxygen index, lower burning rates and better mechanical properties. In particular, the formation of nanocomposites allowed for the recovery of tensile strength reductions caused by high loadings of aluminium tri-hydroxide in the polymer.     

Maleated polypropylene OMMT nanocomposite: Annealing, structural changes, exfoliated and migration

Annealing of maleated polypropylene/organoclay nanocomposites is studied at a range of temperatures from 180 °C to 300 °C under a stream of nitrogen and nitrogen/air mixtures. The study comprises determinations of the migration of clay to the surface by the use of attenuated total reflectance Fourier transform infra red (ATR-FTIR) spectra. The extent of migration is shown to increase with the increase in the percent of maleic anhydride (MA) grafted onto the PP and with the percentage of air added to the nitrogen gas used for purging of the samples during annealing. The extent of migration increases with temperature up to 225 °C. At temperatures of 250-300 °C, the extent of migration decreases. Simultaneously, a change in the structure of the nanocomposites is observed by small-angle X-ray diffraction (XRD), showing a conversion of the nanostructure to the non-colloidal microcomposite. The study conforms to previous findings and indicates that the migrating moiety is composed of exfoliated clay particles. The effect of the decomposition of the grafted MA groups and the evolution of CO₂ on the rate of oxidation and migration are observed and discussed. The effect of the evolved CO₂ on the stability of the clay particles is pointed out. The role of migration in the elucidation of the structure of nanocomposites is discussed along with other mechanistic considerations.