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Phenylene Oxide (phenylene + oxide)
Selected AbstractsSynthesis of well-defined rod-coil block copolymers containing trifluoromethylated poly(phenylene oxide)s by chain-growth condensation polymerization and atom transfer radical polymerizationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2010Yun Jun Kim Abstract Well-defined trifluoromethylated poly(phenylene oxide)s were synthesized via nucleophilic aromatic substitution (SNAr) reaction by a chain-growth polymerization manner. Polymerization of potassium 4-fluoro-3-(trifluoromethyl)phenolate in the presence of an appropriate initiator yielded polymers with molecular weights of ,4000 and polydispersity indices of <1.2, which were characterized by 1H nuclear magnetic resonance spectroscopy and gel permeation chromatography. Initiating sites for atom transfer radical polymerization (ATRP) were introduced at the either side of chain ends of the poly(phenylene oxide), and used for ATRP of styrene and methyl methacrylate, yielding well-defined rod-coil block copolymers. Differential scanning calorimetry study indicated that the well-defined trifluoromethylated poly(phenylene oxide)s showed high crystallinity and were immiscible with polystyrene. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1049,1057, 2010 [source] Liquid-Glassy Polymer Diffusion: Effects of Liquid Molecular Weight and TemperatureMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 10 2007J. Pablo Tomba Abstract We examine mechanistic aspects of the diffusion between a series of liquid polystyrenes (PS) and a glassy poly(phenylene oxide) (PPO) matrix, through the use of confocal Raman microspectroscopy. The results show that the diffusion kinetics has Fickean characteristics, similar to those found in liquid-liquid polymer diffusion. No signatures of the linear regime typical of the case-II diffusion mechanism were found. Overall, these observations are consistent with the claim that case-II is unlikely to occur in liquid-glassy polymer diffusion. [source] Miscibility in Blends of Isotactic/Syndiotactic Polystyrenes at Melt or Quenched Amorphous Solid StateMACROMOLECULAR MATERIALS & ENGINEERING, Issue 11 2006Shu Hsien Li Abstract Summary: Miscibility in amorphous phase and behavior in a crystalline phase of blends of two semicrystalline and isomeric polymers, isotactic polystyrene (iPS) and syndiotactic polystyrene (sPS), was probed. Optical and scanning electron microscopy results indicate no discernible heterogeneity in iPS/sPS blends in either melt state or rapidly quenched amorphous super-cooled state, while the Tg behavior of the quenched amorphous blends shows an intimately mixed state of two polymer chains. The crystal forms of the blends were further analyzed to provide additional evidence of miscibility in the amorphous domain. The sPS in the iPS/sPS blends upon melt crystallization was found to predominantly exist as the more stable , -form (rather than mixed , -form and , -form in neat sPS), which also suggests evidence of miscibility in the iPS/sPS blends. The melting behavior of semicrystalline sPS in the iPS/sPS mixtures was analyzed using the Flory-Huggins approach for estimation of interactions. By measuring the equilibrium melting point of the higher-melting sPS species in the sPS/iPS blends, a small negative value, for the interaction parameter (,,,,,0.11) was found. Further, by introducing a third polymer, poly(2,6-dimethyl- p -phenylene oxide) (PPO), a ternary iPS/sPS/PPO blend system was also proven miscible, which constituted a further test for stable phase miscibility in the iPS/sPS blend. General nature of miscibility in blends composed of two crystalline isomeric polymers is discussed. Issues in dealing with blends of polymers of the same chemical repeat unit but different tacticities were addressed. X-ray diffractograms for neat sPS and iPS/sPS blends, each having been isothermally crystallized at 245,°C for 4 h. [source] Composite thin films of poly(phenylene oxide)/poly(styrene) and PPO/silver via vapor phase depositionPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 10 2009I. S. Bayer Abstract We report fabrication of thin (100,300,nm) poly(phenylene oxide) (PPO) films and their composites with poly (styrene) (PS) and silver (Ag) nanoparticles using a one-step electron beam-assisted vapor phase co-deposition technique. Surface morphology and the structure of the deposited polymer thin film composites were characterized by FTIR, Raman, X-ray spectroscopy, and contact angle measurements. As-deposited PPO films and PPO/Ag composites were of porous nature and contrary to solvent casting techniques were free from nodular growth. In the case of PPO/PS thin film polymer composites, however, film morphology displayed nodular growth of PPO with nodule diameters of about ,200,nm and height of approximately 50,nm. Unique morphological changes on the porous PPO thin film surface were noticed at different Ag filling ratios. Further, the capacitance of PPO/Ag composites (<16 wt%) were measured under radio-frequency conditions and they were functional up to 100,MHz with an average capacitance density of about 2,nF/cm2. The fabricated PPO-based composite systems are discussed for their potential applications including embedded capacitor technology. Copyright © 2008 John Wiley & Sons, Ltd. [source] Sulfonated poly(phenylene oxide) membranes as promising materials for new proton exchange membranesPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 5 2006Shifang Yang Abstract Poly(phenylene oxide) (PPO) was sulfonated to different ion exchange capacities (IECs) using chlorosulfonic acid as the sulfonating agent. Tough, ductile films were successfully cast from sulfonated PPO (SPPO) solutions in N -methyl-2-pyrrolidone or N,N -dimethylformamide. The obtained membranes had good thermal stability revealed by thermogravimetric analysis (TGA). Compared with an unsulfonated PPO membrane, the hydrophilicity and water uptake of the SPPO membranes were enhanced, as shown by reduced contact angles with water. The tensile test indicated that the SPPO membranes with IEC ranging from 0.77 to 2.63,meq/g were tough and strong at ambient conditions and still maintained adequate mechanical strength after immersion in water at room temperature for 24,hr. The results of wide-angle X-ray diffraction (WAXD) showed amorphous structures for PPO and SPPO while the peak intensity decreased after sulfonation. The proton conductivity of these SPPO membranes was measured as 1.16,×,10,2,S/cm at ambient temperature, which is comparable to that of Nafion 112 at similar conditions and in the range needed for high-performance fuel cell proton exchange membranes. Copyright © 2006 John Wiley & Sons, Ltd. [source] Modulation of the Aerobic Oxidative Polymerization in Phenylazomethine Dendrimers Assembling Copper ComplexesCHEMISTRY - A EUROPEAN JOURNAL, Issue 36 2010Dr. Takane Imaoka Abstract The aerobic oxidative polymerization of phenol derivatives can provide poly(phenylene oxide)s, which are known as engineering plastics. This oxidation can be carried out with atmospheric oxygen molecules as the oxidizing reagent in the presence of copper complexes as the catalyst; however, stoichiometric or excess amounts of bases are also generally required. By using a phenylazomethine dendrimer complexed with several equivalent amounts of copper chloride, the additive (base)-free polymerization of 2,6-difluorophenol was successful with a very small amount of the catalyst (0.7,mol,% of copper for the monomer) because the dendrimer was composed of many Schiff base units, affording a base and catalyst (copper complex) condensed reaction field. The resulting polymer was nearly linear and the molecular weight was very high. When the equimolar amount of the copper complex in one dendrimer molecule was increased, the polymer obtained under this reaction condition was rather branched, resulting in a higher glass transition temperature. [source] | ||||||||||