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Optical Microscope Images (optical + microscope_image)
Selected AbstractsUV-Curable Azobenzene Polymer Bearing Photo-Crosslinkable Moiety for Stabilization of Photo-Fabricated Surface Relief StructureMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 16 2002Tatsumi Kimura Abstract In order to find a new class of photo-processable liquid crystalline (LC) aligning material, five kinds of new maleimide-based copolymers bearing both azobenzene and cinnamate moieties with different functionalization ratio have been synthesized. The properties of these five copolymers were compared regarding physical and chemical properties that are required for our aim. The photo-induced surface relief (PSR) gratings could be fabricated on the films of these copolymers using an Ar+ laser (,,=,488 nm), and were successfully immobilized and bleached by UV-light irradiation that causes photo-crosslinking of the cinnamate moiety and photo-degradation of the azobenzene moiety, respectively. The PSR inscription rate and the thermal stability have been investigated regarding the functionalization ratio between cinnamate and azobenzene side chain. The residual ratio of the PSR structure after UV-curing was increased with increasing photo-crosslinkable moiety. It was confirmed that the UV-cured PSR grating structure becomes transparent at visible wavelength and was able to align LC molecules parallel to the grating direction. Polarized optical microscope image of LC cell aligned by the PMPDC 21-18 film with UV-cured PSR structure (0°). [source] Effect of an organic dicarboxylic acid salt on fractionated crystallization of polypropylene dropletsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007Y. Jin Abstract The effect of a particulate nucleating agent on fractionated crystallization of polypropylene (PP) was studied. A novel method utilizing breakup of PP nanolayers was used to obtain a dispersion of PP droplets in a polystyrene (PS) matrix. An assembly with hundreds of PP nanolayers alternating with thicker PS layers was fabricated by layer-multiplying coextusion. The concentration of an organic dicarboxylic acid salt (HPN) nucleating agent in the coextruded PP nanolayers was varied up to 2 wt %. When the assembly was heated into the melt, interfacial driven breakup of the thin PP layers produced a dispersion of PP particles in a PS matrix. Analysis of optical microscope images and atomic force microscope images indicated that layer breakup produced a bimodal particle size distribution of submicron particles and large, micron-sized particles. Almost entirely submicron particles were obtained from breakup of 12 nm PP layers. The fraction of PP as submicron particles dropped dramatically as the PP nanolayer thickness increased to 40 nm. Only large, micron-sized particles were obtained from 200 nm PP nanolayers. The crystallization behavior of the particle dispersions was characterized by thermal analysis and wide angle X-ray diffraction. Only part of the PP was nucleated by HPN. It was found that HPN was not effective in nucleating the population of submicron particles. The particulate HPN was too large to be accommodated in the submicron PP particles. On the other hand, the amount of nucleated crystallization qualitatively paralleled the fraction of PP in the form of large, micron-sized particles. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source] Facile synthesis of polyaniline hemispheres in diethyl ether/ice mixture solvent and growth mechanism studyJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 16 2010Hui-yan Ma Abstract By using the new methodology of synthesis of container structure, we demonstrate the ability to control an improved ice-templating method to synthesis of polyaniline (PANI) in the form of hemisphere. The influence of the synthetic parameters, such as the concentration of doping-acid, oxidant, and aniline on the morphologies of PANI structures, has been investigated. It is determined that the doping acid and the second solvent added (such as diethyl ether absolute) have great positive influence on the formation of product's micro-morphology. The structure and morphology of PANI hemispheres are characterized by Fourier transform infrared (FT-IR) spectra, X-ray diffraction (XRD) patterns, energy-dispersive X-ray analysis (EDX), optical microscope images, and scanning electron microscope images (SEM). The formation mechanism of hemispheres in this article is well suggested. PANI hemispheres have super performance in sensitivity, time response to NH3 compared with traditional polymerization at room temperature. This work extends the field of functional materials with complex container structure and offers a new green route to synthesis of hemispherical container structure. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3596,3603, 2010 [source] Gravimetric method to find internal surface of macroporous silicon membranesPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 6 2007A. A. Nechitailov Abstract A simple method to evaluate the internal surface area, porosity, pore diameter and pore density of macroporous silicon membranes has been proposed and tested. The porosity p is obtained from the mass loss under anodizing, and the surface area per unit volume Sv is determined from the mass of SiO2 formed on the pore surface as a result of thermal oxidation. The average pore diameter d and pore density N can be easily calculated from the obtained Sv and p. Experimental verification of d and N was performed by means of SEM and optical microscope images; Sv was checked by BET technique. Surface area and porosity on the resistivity of initial n-Si in the range , = 3,25 Ohm · cm have been studied for the samples with regular and self-organized macropore "lattices". The obtained values are within the limits p = 27,50%, Sv = 2800,6000 cm2/cm3, d = 1.9,6.5 ,m, N = 1.4,10 × 106 cm,2, and in a good agreement with the data of microscopic characterization. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] | ||||||||||