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Film Preparation (film + preparation)
Selected AbstractsSynthesis of Au@SiO2 Core/Shell Nanoparticles and their Dispersion into an Acrylic Photocurable Formulation: Film Preparation and CharacterizationMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 22 2008Marco Sangermano Abstract Au core/silica shell (Au@SiO2) nanoparticles were synthesized by coating gold NPs with sol/gel silica in alcoholic solution. The alcoholic dispersion was added, in the range of 1,5 wt.-%, to TPGDA and photocured by means of UV light. Transparent coatings were obtained and they can find suitable applications. It was shown that the NPs can restrict the segmental motion and decrease the free volume of the polymer network, with a consequent increase in glass transition temperature. TEM analysis put in evidence that the particles are well dispersed without any macroscopic agglomeration, and many particles are present as isolated particles. [source] Rice bran protein-based edible filmsINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 3 2008Abayomi P. Adebiyi Summary The development of degradable and edible films from protein sources has drawn significant attention for the utilisation of natural resources as well as for the alleviation of the environmental burden. Rice bran protein (RBP) was applied to protein film preparation in this study. The protein solutions were casted on plastic tissue culture dishes with glycerol as a plasticiser after heat treatment. Functional properties of the films were then measured. The puncture strength (PS) of RBP films increased up to pH 8.0 and then decreased. PS of protein films depends on the degree of protein purity, quality and composition. Higher concentration of glycerol weakened the films. The pH affected the water solubility of RBP films and the films showed least solubility at pH 3.0. RBP could be utilised in the preparation of degradable protein-based films. The RBP-based film had functional properties comparable to those of the soy protein-based ones. [source] Fluorescent, molecularly imprinted thin-layer films based on a common polymer,JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007Piotr Cywinski Abstract Fluorescent, molecularly imprinted polymer thin films, with cyclic guanosine 3,,5,-monophosphate (cGMP) as a template and 1,2-diphenyl-6-vinyl-1H -pyrazole-[3,4- b]-quinoline as a fluorescent receptor, were prepared according to a method based on commercially available poly (methyl methacrylate). This method of preparation predicts photoinduced crosslinking in the mixture of polymer chains and involved components. The advantages of this method are the relative simplicity of its preparation and the fact that a common polymer can be used. The spin-coated thin-layer films of imprinted and nonimprinted polymers were studied with the use of fluorescence microscopy with a scanning range of 80 × 80 ,m. A strong fluorescence quenching effect was observed when a cGMP-imprinted film was incubated in aqueous solutions of cGMP, but a comparatively small effect was observed for a nonimprinted polymer and when an imprinted film was incubated with cyclic adenosine 3,,5,-monophosphate (cAMP). The separation factor by the imprinted polymer was determined to be 2.55 for cGMP against cAMP. The obtained polymeric sensor appeared to be stable during subsequent measurements after rewashing and readsorption. The homogeneity of the surface of the polymer film, dependent on the method of film preparation, was also studied. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 105: 229,235, 2007 [source] Monitoring ultrathin film photopolymerization of tetra-alkylepoxyporphyrin by UV-Vis spectroscopyJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 22 2009Kalle Lintinen Abstract Cationic photopolymerization is a convenient in situ polymerization method for organic thin film preparation. In this work, the polymerization mechanisms is applied for highly viscous cross-linking monomers, using tetra-alkylepoxyporphyrin (TAEP) as a case study. By comparing the UV-Vis spectra of the polymerized sample before and after the unreacted monomers have been dissolved, it is possible to estimate the polymerization yield. An IR spectrum of a reference thick film confirms full polymerization. Scanning fluorescence lifetime microscopy and AFM show the uniformity of the polymer. It was shown that photopolymerization is highly dependent on the substrate nature and requires at best case a 10 min illumination at 90 °C. Thermal polymerization of the same sample requires 10 min heating at 150 °C in dark. It was also shown that TAEP works as a self-sensitizer for cationic photopolymerization. The proposed method is a mild and versatile technique for in situ preparation of thin polymeric films directly from chromophore monomers. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 6095,6103, 2009 [source] Control of Induced Chirality in Optically Active Poly(N-propargylcarbamate) Films by Solvent VaporMACROMOLECULAR RAPID COMMUNICATIONS, Issue 15 2009Toshiyuki Fukushima Abstract Chiral polyethyne derivatives with lyotropic liquid-crystalline properties are found to be able to self-assemble, forming two chiral organizations with opposite handedness in solid thin films by selection of the casting solvent and its concentration. After the film preparation, chiral organization could also be induced by simple exposure to an appropriate organic solvent's vapor for several minutes without thermal treatment. Furthermore, irreversible inversion of the handedness of the chiral organization in the film could be achieved by exposure to solvent vapor. [source] Nanofibrous polyaniline thin film prepared by plasma-induced polymerization technique for detection of NO2 gasPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 9 2010Ashutosh Tiwari Abstract A nanofibrous polyaniline (PANI) thin film was fabricated using plasma-induced polymerization method and explored its application in the fabrication of NO2 gas sensor. The effects of substrate position, pressure, and the number of plasma pulses on the PANI film growth rate were monitored and an optimum condition for the PANI thin film preparation was established. The resulting PANI film was characterized with UV,visible spectrophotometer, FTIR, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The PANI thin film possessed nanofibers with a diameter ranging from 15 to 20 nm. The NO2 gas sensing behavior was studied by measuring the change in electrical conductivity of PANI film with respect to NO2 gas concentration and exposure time. The optimized sensor exhibited a sensitivity factor of 206 with a response time of 23 sec. The NO2 gas sensor using nanofibrous PANI thin film as sensing probe showed a linear current response to the NO2 gas concentration in the range of 10,100 ppm. Copyright © 2009 John Wiley & Sons, Ltd. [source] | ||||||||||