Effect of Hot Band Annealing on Magnetic Properties in 3% Si Grain‐oriented Electrical Steels

Hot band annealing is known to be a prerequisite for good magnetic properties irrespective of manufacturing methods in grain‐oriented Fe‐3 wt.% Si electrical steels. In this study, the effects of hot band annealing on magnetic properties were investigated in 3% grain‐oriented electrical steels of low soluble AI contents and one‐stage cold rolling. Microstructure and precipitate distribution were compared with hot band annealing conditions. Secondary recrystallization behaviour with hot band annealing condition was also discussed.     

Surface oxidation of styrene butadiene copolymers: Study by laser ablation and secondary ion mass spectrometry

The capabilities of ion bombardment and laser ablation coupled to mass spectrometry as independent techniques to investigate the surface thermooxidative stability of polystyrene, polybutadiene polymers, and styrene butadiene rubber (SBR) copolymers were investigated. Surface chemical modifications were detected according to the polymeric structure. The degradation products detected by static secondary ion mass spectrometry appeared at m/z 29, 43, and 55. Their compositions were related to the general formulae C_nH_mO⁺ with n = 1–3 and m = 1–3 for polybutadiene and styrene butadiene copolymers, whereas polystyrene was not affected by the aging treatment. The C_nH_mO⁺ ions result from butadiene unit degradation. The laser ablation ionization Fourier transform ion cyclotron resonance mass‐spectrometry results confirmed the detection of C_nH_mO⁺ ions. Finally, it may be considered that the surface thermooxidative process of SBR copolymers begins with butadiene unit degradation. The development of butadiene unit oxidation showed a dynamic oxidation phase, which coincided with a loss of unsaturation. The influence of the polymer conformation (blocked, branched, and random) on the surface oxidation for 30% styrene SBR compounds was also studied. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1910–1917, 2003     

The characteristic properties of poly(methyl methacrylate)/polystyrene core‐shell composite polymer latex

In this study, the poly(methyl methacrylate/polystyrene (PMMA/PS) core‐shell composite latex was synthesized by the method of soapless seeded emulsion polymerization. The morphology of the PMMA/PS composite latex was core‐shell structure, with PMMA as the core and PS as the shell. The core‐shell morphology of the composite polymer latex was found to be thermally unstable. Under the effect of thermal annealing, the PS shell region first dispersed into the PMMA core region, and later separated out to the outside of the PMMA core region. This was explained on the basis of lowing interfacial tension between the PMMA and PS phases owing to the interpenetration layer. The interpenetration layer, which was located at the interface of the core and shell region, contained graft copolymer and entangled polymer chains. Both the graft copolymer and entangled polymer chains had the ability to lower the interfacial tension between the PMMA and PS phases. Also, the effect of thermal annealing on the morphology of commercial polymer/composite latex polymer blends was examined. The result showed that the core‐shell composite latex had the ability to enhance the compatibility of the components of polymer blends. The compatibilizing ability of the core‐shell composite latex was better than that of a random copolymer. Moreover, the effect of the amount of core‐shell composite latex on the morphology of the polymer blend was investigated. The polymer blends, which contained composite latex above 50% wt, showed the morphology of a double sea‐island structure. In addition, the composite latex was completely dissolved in solvent to destroy the core‐shell structure and release the entangled polymer chains, and then dried to form the entangled free composite polymer. The entangled free composite polymer had the ability to enhance the compatibility of the components of the polymer blend as usual. The weight ratio 3/7 commercial polymer/entangled free composite polymer blend showed the morphology of the phase inversion structure. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 312–321, 2003     

Synthesis,structures, and properties of side‐chain cholesteric liquid‐crystalline polysiloxanes

The synthesis of three cholesteric monomers and side‐chain liquid‐crystalline polymers was described. The structure–property relationships of monomers IM–IIIM and polymers IP–IIIP were discussed. Their phase behavior and optical properties were investigated by differential scanning calorimetry, thermogravimetric analyses (TGA), and polarizing optical microscopy. Monomers IM–IIIM exhibited cholesteric oily‐streak texture and focal‐conic texture. Polymers IIP and IIIP revealed smectic A fan‐shaped texture and cholesteric grandjean texture, respectively. Experimental results demonstrated that the selective reflection of IM–IIIM shifted to the short‐wavelength region with increasing the flexible spacer length or decreasing the rigidity of the mesogen. Polymers with a longer flexible spacer had lower glass‐transition temperatures and wider mesomorphic temperature ranges. TGA showed that the temperatures at which 5% weight loss occurred were greater than 300°C for all the polymers. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3944–3950, 2003     

Melting process and mechanism for vibration induced single‐screw extruder

The effect of a vibration force field on the melting process of an extruder is studied. It is shown that the mechanism for melting differs from conventional theory. Experimental studies of melting of low‐density polyethylene (LDPE) pellets in a vibration‐induced single‐screw (VISS) extruder show that melting is initiated on the inside of the barrel and the surface of screw. Models were developed that explain the melting mechanism in those regions. The melting at the surface of the screw is mainly initiated by frictional work on the pellets by the vibration and rotation of the screw. The melting action at the barrel is induced by a barrel temperature higher than the melting point and propagated by viscous dissipation heating of the melt film produced. The theory is supplemented by a calculation sample, which shows good agreement with experimental data obtained on a transparent barrel VISS (T‐VISS) extruder and a half‐open barrel VISS (H‐VISS) extruder with LDPE. The results of the experiment and calculation sample indicate that the introduction of vibration‐induced field can improve the melting capacity of extruder to a great extent. The present model enables the prediction of processing parameters for VISS extruders, from which the optimum operating conditions can be obtained. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2504–2514, 2007     

Preparation,characterization, and some physical properties of polypropylene/poly(methyl acrylate)‐grafted glass wool composites

Polypropylene/poly(methyl acrylate)‐grafted glass wool (PMA‐g‐GW) mixes were prepared. The polymerization process was carried out using potassium persulfate (PPS) and PPS/acetone sodium bisulfite (ASBS) as a redox‐pair initiation system at 60 and 70°C. The effect of using PPS or PPS/ASBS on the grafting percent and conversion percent reveals that the conversion percent values on using PPS as an initiator are higher than those of PPS/ASBS, while in the case of grafting, the inverse is true, that is, using PPS as an initiator gives grafting percent values lower than those that can be obtained using PPS/ASBS. The dielectric properties, thermal diffusivity, specific heat capacity, and thermal conductivity of PP loaded with modified glass wool as a function of different types and concentrations of initiators—used in the grafting polymerization process, namely, PPS and the redox initiating system—were also studied. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 723–732, 2003     

Monodisperse polymer/metal composite particles by electroless chemical deposition: Effect of surface functionality of polymer particles

Micron‐sized polymer particles were coated with layers of nickel compounds by plating electrolessly in the presence of aqueous solutions of nickel chloride, sodium hypophosphite, sodium citrate, and ammonium chloride at elevated temperature. The uniform functional polymer particle could be obtained by seeded polymerization. To investigate the effect of surface functionality on the conditions for nickel deposition, the polymer particle was functionalized with the thiol group. From morphological observation, it was found that the mode of nickel deposition was greatly dependent on the surface functionality of the polymer particle. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 420–424, 2003     

Derivation of a Retinoid X Receptor Scaffold from Peroxisome Proliferator‐Activated Receptor γ Ligand 1‐Di(1H‐indol‐3‐yl)methyl‐4‐trifluoromethylbenzene

PPARγ agonist DIM‐Ph‐4‐CF ₃ , a template for RXRα agonist (E)‐3‐[5‐di(1‐methyl‐1H‐indol‐3‐yl)methyl‐2‐thienyl] acrylic acid: DIM‐Ph‐CF₃ is reported to inhibit cancer growth independent of PPARγ and to interact with NR4A1. As both receptors dimerize with RXR, and natural PPARγ ligands activate RXR, DIM‐Ph‐4‐CF₃ was investigated as an RXR ligand. It displaces 9‐cis‐retinoic acid from RXRα but does not activate RXRα. Structure‐based direct design led to an RXRα agonist.