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Polystyrene Matrix (polystyrene + matrix)
Selected AbstractsImprovement of the interfacial compatibility between sugar cane bagasse fibers and polystyrene for compositesPOLYMER COMPOSITES, Issue 2 2004Edgar García-Hernández Sugar cane bagasse fibers were modified by surface treatments using either physical or chemical methods in order to improve their adhesion to polystyrene matrices. The surface treatment methods used were alkaline treatment, treatment with silane coupling agents, physical coating with polystyrene and grafting of polystyrene with and without crosslinker. Fiber modifications were monitored by Fourier Transform Infrared Spectroscopy (FTIR), Differential Thermal Analysis coupled with Thermogravimetric Analysis (DTA-TGA) and Scanning Electron Microscopy (SEM). On the other hand, the improvement of the adhesion between sugar cane modified fibers and polystyrene was assessed by micromechanical pull-out and by macromechanical Iosipescu tests. It was found, from Interfacial Shear Strength values (IFSS), that substantial improvements in fiber-matrix compatibility were achieved. According to micro- and macromechanical test results, the IFSS increased for all treated fibers as compared to non-treated fibers. Particularly, both the coating the fibers or grafting with polystyrene using crosslinker resulted in substantial adhesion improvement to the polystyrene matrix in comparison with the non-treated fibers and fibers treated by alkaline and silane methods only. Polym. Compos. 25:134,145, 2004. © 2004 Society of Plastics Engineers. [source] Electrode Modified with Cobalt Cyclohexylbutyrate for the Determination of Low Molecular Weight Thiol Group Bearing Compounds Using Catalytic Stripping VoltammetryELECTROANALYSIS, Issue 3 2010Petr Jakubec Abstract Glassy carbon electrode, modified with cobalt(II) cyclohexylbutyrate monohydrate immobilized in polystyrene matrix is usable for determination of thiol group bearing compounds both in oxidized and reduced forms using catalytic stripping voltammetry. The measurements are carried out in acetate buffer (pH,4.3) containing Tween 40. After the accumulation step at ,850,mV vs. Ag/AgCl a peak at ,170,mV is observed on linear sweep voltammogram, the height of which is proportional to the concentration of added thiol. Addition of carbon nanotubes into polystyrene film enhances the sensitivity of the modified electrode. The detection limit is 1×10,6,mol dm,3 for all studied thiols. The electrode can be regenerated by exposing it to the potential between 300,600,mV. [source] Macroscopically Aligned Ionic Self-Assembled Perylene-Surfactant Complexes within a Polymer Matrix,ADVANCED FUNCTIONAL MATERIALS, Issue 13 2008Ari Laiho Abstract Ionic self-assembled (ISA) surfactant complexes present a facile concept for self-assembly of various functional materials. However, no general scheme has been shown to allow their overall alignment beyond local polydomain-like order. Here we demonstrate that ionic complexes forming a columnar liquid-crystalline phase in bulk can be aligned within polymer blends upon shearing, taken that the matrix polymers have sufficiently high molecular weight. We use an ISA complex of N,N,-bis(ethylenetrimethylammonium)perylenediimide/bis(2-ethylhexyl) phosphate (Pery-BEHP) blended with different molecular weight polystyrenes (PS). Based on X-ray scattering studies and transmission electron microscopy the pure Pery-BEHP complex was found to form a two-dimensional oblique columnar phase where the perylene units stack within the columns. Blending the complex with PS lead to high aspect ratio Pery-BEHP aggregates with lateral dimension in the mesoscale, having internal columnar liquid-crystalline order similar to the pure Pery-BEHP complex. When the Pery-BEHP/PS blend was subjected to a shear flow field, the alignment of perylenes can be achieved but requires sufficiently high molecular weight of the polystyrene matrix. The concept also suggests a simple route for macroscopically aligned nanocomposites with conjugated columnar liquid-crystalline functional additives. [source] Polythiophene-Fullerene Based Photodetectors: Tuning of Spectral Response and Application in Photoluminescence Based (Bio)Chemical SensorsADVANCED MATERIALS, Issue 37 2010Kanwar S. Nalwa A photoluminescence (PL)-based oxygen and glucose sensor utilizing inorganic or organic light emitting diode as the light source, and polythiophene:fullerene type bulk-heterojunction devices as photodetectors, for both intensity and decay-time based monitoring of the sensing element's PL. The sensing element is based on the oxygen-sensitive dye Pt-octaethylporphyrin embedded in a polystyrene matrix. [source] Photoinitiated polymerization of methacrylic monomers in a polystyrene matrix: Kinetic, mechanistic, and structural aspectsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2001J. L. Mateo Abstract The kinetics and mechanism of the photoinitiated polymerization of tetrafunctional and difunctional methacrylic monomers [1,6-hexanediol dimethacrylate (HDDMA) and 2-ethylhexyl methacrylate (EHMA)] in a polystyrene (PS) matrix were studied. The aggregation state, vitreous or rubbery, of the monomer/matrix system and the intermolecular strength of attraction in the monomer/matrix and growing macroradical/matrix systems are the principal factors influencing the kinetics and mechanism. For the PS/HDDMA system, where a relatively high intermolecular force of attraction between monomer and matrix and between growing macroradical and matrix occurs, a reaction-diffusion mechanism takes place at low monomer concentrations (<30,40%) from the beginning of the polymerization. For the PS/EHMA system, which presents low intermolecular attraction between monomer and matrix and between growing macroradical and matrix, the reaction-diffusion termination is not clear, and a combination of reaction-diffusion and diffusion-controlled mechanisms explains better the polymerization for monomer concentrations below 30,40%. For both systems, for which a change from a vitreous state to a rubbery state occurs when the monomer concentration changes from 10 to 20%, the intrinsic reactivity and kp/kt1/2 ratio (where kp is the propagation kinetic constant and kt is the termination kinetic constant) increase as a result of a greater mobility of the monomer in the matrix (a greater kp value). The PS matrix participates in the polymerization process through the formation of benzylic radical, which is bonded to some extent by radical,radical coupling with the growing methacrylic radica, producing grafting on the PS matrix. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 2049,2057, 2001 [source] In Vivo Phosphorescence Imaging of pO2 Using Planar Oxygen SensorsMICROCIRCULATION, Issue 6 2005PHILIPP BABILAS ABSTRACT Objective: Oxygen-dependent quenching of luminescence of metal porphyrin complexes has been used to image the pO2 distribution over tumor and normal tissue. Methods: An experimental setup is described using a platinum(II),octaethyl,porphyrin immobilized in a polystyrene matrix as transparent planar sensor. Results: Sensitivity over a broad range is high at low pO2 values (± 0.2 mm Hg at 0 mm Hg; ± 1.5 mm Hg at 160 mm Hg pO2). Due to intrinsically referencing via lifetime encoding there was no modification of the sensor response in vivo in the dorsal skinfold chamber model with amelanotic melanoma (A-MEL-3) in awake hamsters when compared to the in vitro calibration. pO2 measurements over normal tissue (25.8 ± 5.1 mm Hg) and tumor tissue (9.2 ± 5.1 mm Hg) were in excellent agreement with previous results obtained in this model using a surface multiwire electrode. Conclusions: Using the presented method the surface pO2 distribution can be mapped with a high temporal resolution of approximately 100 ms and a spatial resolution of at least 25 , m. Moreover, the transparent sensor allows the simultaneous visualization of the underlying microvasculature. [source] Holographic properties of azobenzene oligomers with differently bonded chromophore groupsPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 3 2007A. Ozols Abstract Holographic properties of two types (I and II, specified in the text) of azobenzene oligomers (ABO) have been experimentally studied in the spectral region of low absorption at 633 nm. In the case of type I ABO the chromophore groups were covalently bonded to either tolyl-polyurethane or hexamethylene-polyurethane matrix. In the case of type II ABO azobenzene chromophores were dispersed in polystyrene matrix, and their concentration was varied from 0.005 to 0.200 mol/l. Samples were in the form of 10 µm thick films. In both cases the diffraction efficiency exposure time dependences were measured for the holographic grating period of 2 (m at 633 nm. The diffraction efficiency of more than 2% and the specific recording energy down to 30 - 60 J/(cm2%) were achieved in both cases. In the case of type I ABO the best results were achieved with 4-nitronaphtylazobenzene chromophore groups in hexamethylene-polyurethane matrix. The chromophore concentration threshold within 0.01 , 0.04 mol/l range, the holographic efficiency growth with chromophore concentration and the photosensitization effect were found in the case of type II ABO. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Improvement of the interfacial compatibility between sugar cane bagasse fibers and polystyrene for compositesPOLYMER COMPOSITES, Issue 2 2004Edgar García-Hernández Sugar cane bagasse fibers were modified by surface treatments using either physical or chemical methods in order to improve their adhesion to polystyrene matrices. The surface treatment methods used were alkaline treatment, treatment with silane coupling agents, physical coating with polystyrene and grafting of polystyrene with and without crosslinker. Fiber modifications were monitored by Fourier Transform Infrared Spectroscopy (FTIR), Differential Thermal Analysis coupled with Thermogravimetric Analysis (DTA-TGA) and Scanning Electron Microscopy (SEM). On the other hand, the improvement of the adhesion between sugar cane modified fibers and polystyrene was assessed by micromechanical pull-out and by macromechanical Iosipescu tests. It was found, from Interfacial Shear Strength values (IFSS), that substantial improvements in fiber-matrix compatibility were achieved. According to micro- and macromechanical test results, the IFSS increased for all treated fibers as compared to non-treated fibers. Particularly, both the coating the fibers or grafting with polystyrene using crosslinker resulted in substantial adhesion improvement to the polystyrene matrix in comparison with the non-treated fibers and fibers treated by alkaline and silane methods only. Polym. Compos. 25:134,145, 2004. © 2004 Society of Plastics Engineers. [source] Deformation mechanism of polystyrene toughened with sub-micrometer monodisperse rubber particlesPOLYMER INTERNATIONAL, Issue 11 2006Guanghui Gao Abstract Core,shell polybutadiene- graft -polystyrene (PB- g -PS) rubber particles with different ratios of polybutadiene to polystyrene were prepared by emulsion polymerization through grafting styrene onto polybutadiene latex. The weight ratio of polybutadiene to polystyrene ranged from 50/50 to 90/10. These core-shell rubber particles were then blended with polystyrene to prepare PS/PB- g -PS blends with a constant rubber content of 20 wt%. PB- g -PS particles with a lower PB/PS ratio (,70/30) form a homogeneous dispersion in the polystyrene matrix, and the Izod notched impact strength of these blends is higher than that of commercial high-impact polystyrene (HIPS). It is generally accepted that polystyrene can only be toughened effectively by 1,3 µm rubber particles through a toughening mechanism of multiple crazings. However, the experimental results show that polystyrene can actually be toughened by monodisperse sub-micrometer rubber particles. Scanning electron micrographs of the fracture surface and stress-whitening zone of blends with a PB/PS ratio of 70/30 in PB- g -PS copolymer reveal a novel toughening mechanism of modified polystyrene, which may be shear yielding of the matrix, promoted by cavitation. Subsequently, a compression-induced activation method was explored to compare the PS/PB- g -PS blends with commercial HIPS, and the result show that the toughening mechanisms of the two samples are different. 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