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Total Reflectance Spectroscopy (total + reflectance_spectroscopy)
Selected AbstractsPotential Modulated Attenuated Total Reflectance Spectroscopy of Prussian Blue Films on ITOISRAEL JOURNAL OF CHEMISTRY, Issue 3 2006Zeynep Ozkan Araci Potential modulated attenuated total reflectance (PM-ATR) spectroscopy has been employed to study charge transfer processes in Prussian blue (PB) films deposited on indium tin oxide (ITO) electrodes. PM-ATR is a planar waveguide-based spectroelectrochemical technique in which the optical response of an electroactive film is measured as a function of applied potential and modulation frequency. The multiple internal reflection geometry of PM-ATR provides a significant sensitivity advantage over the single external reflectance geometry that has been employed in most prior electroreflectance studies. The apparent electron transfer rate of PB on ITO obtained using PM-ATR was compared to that obtained with conventional cyclic voltammetry; the respective rates, 0.33 ± 0.15 s,1 (n = 3) and 0.71 ± 0.37 s,1 (n = 10), are in good agreement. [source] Comparison of poly(o -anisidine) and poly(o -anisidine- co -aniline) copolymer synthesized by chemical oxidative methodJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010J. Longun Abstract In this study, poly(o -anisidine) [POA], poly(o -anisidine- co -aniline) [POA- co -A], and polyaniline [PANi] were chemically synthesized using a single polymerization process with aniline and o -anisidine as the respective monomers. During the polymerization process, p -toluene sulfonic acid monohydrate was used as a dopant while ammonium persulfate was used as an oxidant. N -methyl-pyrolidone (NMP) was used as a solvent. We observed that the ATR spectra of POA- co -A showed features similar to those of PANi and POA as well as additional ones. POA- co -A also achieved broader and more extended UV,vis absorption than POA but less than PANi. The chemical and electronic structure of the product of polymerization was studied using Attenuated Total Reflectance spectroscopy (ATR) and UV,visible spectroscopy (UV,vis). The transition temperature of the homopolymers and copolymers was studied using differential scanning calorimetry and the viscosity average molecular weight was studied by using dilute solution viscometry. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Effect of accelerated aging on the structure and properties of monolayer and multilayer packaging filmsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008P. A. Tarantili Abstract The effect of accelerated aging on the structure and properties of single, metalized, and multilayer films used in food packaging was studied through the exposure of specimens of those films to repeated aging cycles in a weather meter under the combined action of ultraviolet, humidity, and heat. The aged specimens were tested for their mechanical properties and water vapor transmission characteristics, and the results were compared to those obtained from the original specimens. The property changes introduced into the films by aging were further explored by attenuated total reflectance spectroscopy and differential scanning calorimetry in an attempt to correlate the changes in the properties with structural characteristics. The results showed that the films made of polypropylene (PP) underwent severe chain scission upon irradiation and lost mechanical properties but still retained their impermeability to water vapor. The metallic coating could not prevent PP from degrading, as it seemed to oxidize under the aging conditions. Therefore, the metalized film showed the same mechanical response as PP, but its water impermeability dropped dramatically. Polyethylene (PE) and poly(ethylene terephthalate) (PET) films showed modest decreases in their mechanical properties, which could be attributed to crosslinking reactions taking place with PE and to the increased ultraviolet stability of PET, respectively. On the other hand, the multilayer films presented a decrease in their mechanical properties according to those of their weak component, which would be expected for a composite structure. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Conformational changes of enzymes adsorbed at liquid, solid interface: Relevance to enzymatic activityBIOPOLYMERS, Issue 4-5 2002S. Noinville Abstract FTIR with attenuated total reflectance spectroscopy was used to study in situ adsorption of enzymes at water,solid interfaces to better understand how conformational changes may monitor enzymatic activity. Because the adsorption process depends on hydrophobic and electrostatic interactions, conformational changes were studied as a function of the nature of the adsorbing substrates, which are hydrophobic or hydrophilic in character. The adsorption kinetics of two examples of serine enzymes, ,-chymotrypsin (,-chym) and Humicola lanuginosa lipase (HLL), were studied. The secondary structure and solvation of the adsorbed enzymes were both compared to the dissolved enzymes. The positively charged ,- chym was adsorbed on a negatively charged hydrophilic support with minor structural changes, but the negatively charged lipase had no affinity for a similar support. Both enzymes were strongly retained on the hydrophobic support. The secondary and tertiary structures of the ,-chym adsorbed on the hydrophobic support were strongly altered, which correlates to the inhibition of enzymatic hydrolysis. The specific solvation obtained for the adsorbed HLL is consistent with the existence of the open conformer in relation to the enhanced enzymatic activity at the water,hydrophobic interface. © 2002 Wiley Periodicals, Inc. Biopolymers (Biospectroscopy) 67: 323,326, 2002 [source] | ||||||||||