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FTIR spectra of polymers

The GC electrodes (3 mm diameter) were purchased from bioanalytical science. The cyclic voltammetiy was performed with a bioanalytical system (BAS) potentiostat (Model 100). In the voltammetric experiments, a three-electrode configuration was used, including Ag/AgCl reference electrode and a platinum wire counter electrode. The reflectance fourier transform infrared (FTIR) spectra of polymers were obtained using Nicolet NEXUS 870 FTIR instrument. The UV-vis. spectra use an Agilent 8453 spectrophotometer. [Pg.176]

Interspectrum. Fireash Data Management (FDM) FTIR Spectra of Polymers and Polymer Additives (580 Spectra). Toravere, Tartumaa, Estonia. Available at http // www.interspectrum.ee. [Pg.116]

FIGURE 3.5 Fourier Transform infrared (FTIR) spectra of acrylic rubber (ACM)-siUca hybrid nanocomposites. The numbers after ACM (10 and 50) indicate the wt% tetraethoxysilane (TEOS) concentration. The letters preceding the numbers indicate the ACM-silica samples cross-linked from benzoyl peroxide (B) and a mixed cross-linker hexamethylene diamine carbamate and ammonium benzoate (D). The numbers over the absorption peaks are the wave numbers corresponding to absorbance of those peaks. (From Bandyopadhyay, A., Bhowmick, A.K., and De Sarkar, M., J. Appl. Polym. Sci., 93, 2579, 2004. Courtesy of Wiley InterScience.)... [Pg.64]

SFC-based methods still need to show their potential, in spite of past great promise. pSFC-APCI-MS is a powerful method for identification of polymer additives, provided that a library of mass spectra of polymer additives using this technique is available. SFC-MS appears less performing than originally announced nevertheless, SFE-SFC-EIMS is an interesting niche approach to additive analysis. On the other hand, we notice the lack of real breakthrough in SFE-SFC-FTIR. [Pg.735]

Fig. 3 FTIR spectra of monomer EDOT and polymer PEDOT in the presence of PSSNa. (Reprinted with permission from Bruno et al. [37]. 2006, American Chemical Society)... Fig. 3 FTIR spectra of monomer EDOT and polymer PEDOT in the presence of PSSNa. (Reprinted with permission from Bruno et al. [37]. 2006, American Chemical Society)...
X-ray photoelectron spectroscopy (XPS) was used for elemental analysis of plasma-deposited polymer films. The photoelectron spectrometer (Physical Electronics, Model 548) was used with an X-ray source of Mg Ka (1253.6 eV). Fourier transform infrared (FTIR) spectra of plasma polymers deposited on the steel substrate were recorded on a Perkin-Elmer Model 1750 spectrophotometer using the attenuated total reflection (ATR) technique. The silane plasma-deposited steel sample was cut to match precisely the surface of the reflection element, which was a high refractive index KRS-5 crystal. [Pg.463]

Raman is simple to use and require virtually no sample preparation. The vibrational spectra of polymer samples in their original forms can be measured and casting or hotpressing of the material into thin films (commonly used for FTIR measurements), a very time-consuming procedure that can affect the original structure of the material, are not required. It also offers remote analysis capabilities if combined with fibre optics [108, 109]. Accurate determination of contaminant content in recycled polymeric resins have been reported in the literature [110, 111, 112]. [Pg.217]

Figure 2.2 Single beam PA-FTIR spectra of MTEC carbon-filled polymer... Figure 2.2 Single beam PA-FTIR spectra of MTEC carbon-filled polymer...
Unfortunately, temperature dependent UV-Vis spectra of polymers, 31, were not reported. Films of the polymers were irradiated (medium-pressure Hg lamp) and the reactions monitored by UV-Vis and FTIR spectroscopy. Homopolymer, 31 (jc = 6), was irradiated at 120°C in the N phase. A gradual decrease in the main absorption band of the chromophore at 352 nm was observed and the film eventually became completely insoluble. Interestingly, no initial increase in absorbance was observed, as had been seen for a small molecule LC model and for MCLC polymers [64] 30 (vide supra) and previously attributed to disruption of... [Pg.163]

Fig. 2 i FTIR spectra of 0.1 xm silica particles in radius (a) bare (b) with chemisorbed GPS (c) with grafted PS ii Calibration plot for PS grafted layer in the mixture of PS powder with silica particles o 0.1 xm and A 1.2 urn in radius in terms of the FTIR spectrum integral absorbance vs. mass fraction of the polymer... [Pg.76]

Faix O, Beinhoff O (1988) FTIR spectra of milled wood lignins and lignin polymer models (DHPs) with enhanced resolution obtained by deconvolution J Wood Chem Technol... [Pg.106]

Figure 11.8 FTIR spectra of plasma polymers prepared by cascade arc torch from (a) tetramethydisiloxane (TMDSO), (b) hexamethydisiloxane (HMDSO), and (c) vinylpenta-methyldisiloxane (VpMDSO) 750 seem argon, 4.0 A arc current, 5.0 seem monomers. Figure 11.8 FTIR spectra of plasma polymers prepared by cascade arc torch from (a) tetramethydisiloxane (TMDSO), (b) hexamethydisiloxane (HMDSO), and (c) vinylpenta-methyldisiloxane (VpMDSO) 750 seem argon, 4.0 A arc current, 5.0 seem monomers.
Tailor-made materials require access to linear as well as to branched macro-molecular structures. FTIR spectra of the polymer and GC analysis of the oligomers in solution (if present) can be used for characterization and as a reference for structural changes. [Pg.13]

The FTIR spectra showed that the aerosols formed contained hydrates, polymeric forms, acetals and hemiacetals. Several peaks in these spectra closely corresponded to peaks in FTIR spectra of aerosols collected in the Smoky Mountains (Jang et al. 2002). Czoschke et al. (2003) concluded, that in their experiments, isoprene had been oxidised to aldehydes by ozone in the gas phase, and the aldehydes had been converted to the observed products in heterogeneous, acid-catalysed reactions. However, the presented analysis of aerosol yields was very approximate, and did not exclude the possibility of heterogeneous reactions of isoprene in the discussed experiments. All the differences in reactors and techniques given, in the experiments by Limbeck et al. (2003) ozone reacted with isoprene in the gas phase, but decreased the amount of polymers formed. [Pg.264]

O Falx and O Beinhoff. Ftir Spectra of Milled Wood Lignins and Lignin Polymer Models (DHP s) with Enhanced Resolution Obtained by Deconvolution. J. Wood Chem. Technol. 8 505-522, 1988. [Pg.135]


See other pages where FTIR spectra of polymers is mentioned: [Pg.403]    [Pg.306]    [Pg.403]    [Pg.306]    [Pg.71]    [Pg.20]    [Pg.448]    [Pg.35]    [Pg.93]    [Pg.416]    [Pg.119]    [Pg.152]    [Pg.108]    [Pg.349]    [Pg.396]    [Pg.79]    [Pg.95]    [Pg.997]    [Pg.231]    [Pg.960]    [Pg.422]    [Pg.315]    [Pg.712]    [Pg.395]    [Pg.326]    [Pg.333]    [Pg.184]    [Pg.189]    [Pg.140]    [Pg.226]   
See also in sourсe #XX -- [ Pg.184 , Pg.189 ]




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Spectra of polymers

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