Infrared spectroscopy poly

Poly(vinyl acetate). The dielectric and mechanical spectra of hybrids produced by mixing a poly(vinyl acetate)—THE solution with TEOS, followed by the addition of HCl have been investigated (45). Mixtures were made which were beheved to be 0, 5, 10, 15, and 20 wt % Si02, respectively. These composites were transparent and Eourier transform infrared spectroscopy (ftir) revealed hydrogen bonding between the siUcate network and carbonyl units of the poly(vinyl acetate) (PVAc). No shift in the T of the composites from that of the pure PVAc was observed. Similarly, the activation... 

Infrared spectroscopy. Due to experimental difficulties, infrared spectroscopy is used infrequently in these kinetic studies. However, continuous measurements have been carried out by Schumann28 in the study of the poly(ethylene terepthalate) synthesis. 

The structure of poly(iminocarbonates) synthesized by the direct interfacial polymerization of BPA and cyanogen bromide was analyzed by NMR, Fourier transform infrared spectroscopy and elemental analysis and found to be identical in all aspects to authentic poly(imino-carbonates) obtained by solution polymerization (46). 

Mori, S., Determination of the composition and molecular-weight distribution of a poly(vinyl chloride-vinyl acetate) co-polymer by gel permeation chromatography and infrared spectroscopy, ]. Chromatogr., 157, 75, 1978. 

V.A. Basiuk and J. Douda, Pyrolysis of poly glycine and poly 1 alanine analysis of less volatile products by gas chromatography/Fourier Transform infrared spectroscopy/mass spectrometry, J. Anal. Appl. Pyrol., 55, 235 236 (2000). 

Infrared spectroscopy has been widely used for the qualitative and quantitative characterization of polymorphic and pseudopolymorphic compounds of pharmaceutical interest. Since solid state IR can be used to probe the nature of (pseudo)polymorphism on the molecular level, this method is particularly useful in instances where full crystallographic characterization of (pseudo)poly-morphism was not found to be possible. Recently, a significant number of publications have appeared that discuss where a multidisciplinary, spectroscopic... 

Gaboury, S. R. Urban, M. W. Analysis of Gas-Plasma-Modified Poly(Dimethylsiloxane) Elastomer Surfaces. Attenuated-Total-Reflectance-Fourier Transform Infrared Spectroscopy. In Structure-Property Relations in Polymers Urban, M. W., Graver, C. D., Eds. Advances in Chemistry Series 236 American Chemical Society Washington, DC, 1993 pp 777-790. 

A mechanistic study by Haynes et al. demonstrated that the same basic reaction cycle operates for rhodium-catalysed methanol carbonylation in both homogeneous and supported systems [59]. The catalytically active complex [Rh(CO)2l2] was supported on an ion exchange resin based on poly(4-vinylpyridine-co-styrene-co-divinylbenzene) in which the pendant pyridyl groups had been quaternised by reaction with Mel. Heterogenisation of the Rh(I) complex was achieved by reaction of the quaternised polymer with the dimer, [Rh(CO)2l]2 (Scheme 11). Infrared spectroscopy revealed i (CO) bands for the supported [Rh(CO)2l2] anions at frequencies very similar to those observed in solution spectra. The structure of the supported complex was confirmed by EXAFS measurements, which revealed a square planar geometry comparable to that found in solution and the solid state. The first X-ray crystal structures of salts of [Rh(CO)2l2]" were also reported in this study. 

Miranda et al. used a combination of Fourier-Transform Infrared Spectroscopy (FT-IR) and PCA to elucidate the chemistry that occurs when poly(vinyl alcohol)... 

A 21.3-g sample of poly(hexamethylene adipamide) is found to contain 2.50 x 10-3 mol of carboxyl groups by both titration with base and infrared spectroscopy. From these data the polymer is calculated to have a number-average molecular weight of 8520. What assumption is made in the calculation How can one experimentally obtain the correct value of M ... 

The investigation of the 300 MHz spectrum of poly(3-methyl-l -butene) indicates that the conclusions drawn by previous workers (2—4) concerning the structures of the crystalline and amorphous polymers are essentially correct the crystalline polymer being almost entirely of the 1,3-structure and the amorphous polymer being a mixture of both 1,2- and 1,3-structures. Further, it has indicated that this method is useful for analysis of the composition of the polymer. Quantitative composition determination, however, has not been carried out, since it is felt that the accuracy of the previous estimates utilizing near infrared spectroscopy were satisfactory. 

The formation of block copolymers from styrene-maleic anhydride and acrylic monomers was also indicated by pyrolytic gas chromatography and infrared spectroscopy. A comparison of the pyrograms of the block copolymers in Figure 7 shows peaks comparable with those obtained when mixtures of the acrylate polymers and poly(styrene-co-maleic anhydride) were pyrolyzed. A characteristic infrared spectrum was observed for the product obtained when macroradicals were added to a solution of methyl methacrylate in benzene. The characteristic bands for methyl methacrylate (MM) are noted on this spectogram in Figure 8. 

Several researchers have combined the separating power of supercritical fluid chromatography (SFC) with more informative spectroscopic detectors. For example, Pinkston et. al. combined SFC with a quadrupole mass spectrometer operated in the chemical ionization mode to analyze poly(dimethylsiloxanes) and derivatized oligosaccharides (7). Fourier Transform infrared spectroscopy (FTIR) provides a nondestructive universal detector and can be interfaced to SFC. Taylor has successfully employed supercritical fluid extraction (SFE)/SFC with FTIR dectection to examine propellants (8). SFC was shown to be superior over conventional gas or liquid chromatographic methods. Furthermore, SFE was reported to have several advantages over conventional liquid solvent extraction (8). Griffiths has published several... 

A polyvinyl acetate latex prepared by semi-continuous polymerization at 55° using a polymethacrylic acid-nonylphenol-poly-ethoxylate phosphate ester emulsifier and sodium persulfate-sodium formaldehyde sulfoxylate initiator (23). The latex was cleaned by ion exchange and serum replacement using both Nuclepore and Pellicon membranes, and the cleaned latex and serum fractions were analyzed by conductometric titration. In addition, the dried films were extracted with water and organic solvents, and the extracts were analyzed by infrared spectroscopy and thermo-gravimetric analysis. 

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