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Fourier Transform Infrared Spectroscopy FTIR

For ESs, FTIR is usually used with TEM, SEM, XRD, BET and other techniques to characterize electrode materials. For example, FTIR is used to examine and chemically confirm the presence of uniform ultrathin polymer layers formed on carbon nanofiber electrodes [52]. FTIR, SEM, and XRD are also used to study surface morphologies of materials, for example, surface changes created during activation of polyacrylonitrile thin films deposited on carbon fibers. Other examples include analysis of CNT electrodes after polyaniline [Pg.310]

Modern FTIR instrument from Thermo Scientific. Source Thermo Scientific Instruments. Direct Industry (online), http //www.directindustry.com/prod/thermo-scientific-scien-tific-instruments/ft-ir-spectrometers-7217-56689.html [accessed March 30, 2012]. With permission.) [Pg.310]

Fourier transform infrared spectroscopy (FTIR) is an effective analytical tool for screening and profiling polymer samples. Infrared spectroscopy is widely used in the analysis and characterization of polymers. Polymer products are not a singular species, but rather, they are a population of polymer molecules varying in composition and configuration plus other added components. [Pg.323]

FTIR spectra of xyloglucan and grafted copolymer were compared. In the case of pure XG, a broad absorption peak at 3450 cm indicates the hydrogen bonded OH [Pg.323]

A Fourier transform infrared spectroscopy (FTIR) study was obtained by using Perkin-Elmer spectrometer 100, USA. Prior to this analysis, kenaf whiskers were mixed with KBr to prepare homogeneous suspensions and afterwards pressed into transparent pellets and analyzed in transmittance mode within the range of 4000-500 cm. In the case of thin nanocomposite film (Cellulose Acetate Butyrate [CAB] and kenaf whiskers) the analysis was done within the range of 4000-500 cm transmittance mode. [Pg.344]

3 Fourier Transform Infrared/Attenuated Total Reflectance Spectroscopy (FTIR/ATR) [Pg.483]

FTIR/ATR permits the examination of the surface on a true monolayer scale. Waveguides bevel-cut from silicon wafers transmit the IR radiation through the reactor via BaF viewports. This allows the vibrational modes of surface molecules and atoms to be studied. [Pg.483]

The strength of IRis the qualitative and sometimes quantitative (with standards) identification of the presence of chemical species, or functional groups, sometimes down to trace levels in liquids and solids. For solids stress, strain, crystallinity/ amorphousity, and inhomogeneities can be detected from absorption peak broaden-ings and shifts. [Pg.273]


Most hydrocarbon resins are composed of a mixture of monomers and are rather difficult to hiUy characterize on a molecular level. The characteristics of resins are typically defined by physical properties such as softening point, color, molecular weight, melt viscosity, and solubiHty parameter. These properties predict performance characteristics and are essential in designing resins for specific appHcations. Actual characterization techniques used to define the broad molecular properties of hydrocarbon resins are Fourier transform infrared spectroscopy (ftir), nuclear magnetic resonance spectroscopy (nmr), and differential scanning calorimetry (dsc). [Pg.350]

The role of specific interactions in the plasticization of PVC has been proposed from work on specific interactions of esters in solvents (eg, hydrogenated chlorocarbons) (13), work on blends of polyesters with PVC (14—19), and work on plasticized PVC itself (20—23). Modes of iateraction between the carbonyl functionaHty of the plasticizer ester or polyester were proposed, mostly on the basis of results from Fourier transform infrared spectroscopy (ftir). Shifts in the absorption frequency of the carbonyl group of the plasticizer ester to lower wave number, indicative of a reduction in polarity (ie, some iateraction between this functionaHty and the polymer) have been reported (20—22). Work performed with dibutyl phthalate (22) suggests an optimum concentration at which such iateractions are maximized. Spectral shifts are in the range 3—8 cm . Similar shifts have also been reported in blends of PVC with polyesters (14—20), again showing a concentration dependence of the shift to lower wave number of the ester carbonyl absorption frequency. [Pg.124]

In this chapter, three methods for measuring the frequencies of the vibrations of chemical bonds between atoms in solids are discussed. Two of them, Fourier Transform Infrared Spectroscopy, FTIR, and Raman Spectroscopy, use infrared (IR) radiation as the probe. The third, High-Resolution Electron Enetgy-Loss Spectroscopy, HREELS, uses electron impact. The fourth technique. Nuclear Magnetic Resonance, NMR, is physically unrelated to the other three, involving transitions between different spin states of the atomic nucleus instead of bond vibrational states, but is included here because it provides somewhat similar information on the local bonding arrangement around an atom. [Pg.413]

This is a nonpolar rubber with very little unsamration. Nanoclays as well as nanotubes have been used to prepare nanocomposites of ethylene-propylene-diene monomer (EPDM) rubber. The work mostly covers the preparation and characterization of these nanocomposites. Different processing conditions, morphology, and mechanical properties have been smdied [61-64]. Acharya et al. [61] have prepared and characterized the EPDM-based organo-nanoclay composites by X-ray diffracto-gram (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy... [Pg.35]

In the present study, we synthesized in zeolite cavities Co-Mo binary sulfide clusters by using Co and Mo carbonyls and characterized the clusters by extended X-ray absorption fine structure (EXAFS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), and high resolution electron microscopy (HREM). The mechanism of catalytic synergy generation in HDS is discussed. [Pg.503]

Figure 5.11 (Crisp Wilson, 1974b) shows the time-dependent variation of the concentration of soluble ions in setting and hardening cements. Note that the concentrations of aluminium, calcium and fluoride rise to maxima as they are released from the glass. After the maximum is reached the concentration of soluble ions decreases as they are precipitated. Note that this process is much more rapid for calcium than for aluminium and the sharp decline in soluble calcium corresponds to gelation. This indication is supported by information from infrared spectroscopy which showed that gelation (initial set) was caused by the precipitation of calcium polyacrylate. This finding was later confirmed by Nicholson et al. (1988b) who, using Fourier transform infrared spectroscopy (FTIR), found that calcium polyacrylate could be detected in the cement paste within one minute of mixing the cement. There was no evidence for the formation of any aluminium polyacrylate within nine minutes and substantial amounts are not formed for about one hour (Crisp et al, 1974). Figure 5.11 (Crisp Wilson, 1974b) shows the time-dependent variation of the concentration of soluble ions in setting and hardening cements. Note that the concentrations of aluminium, calcium and fluoride rise to maxima as they are released from the glass. After the maximum is reached the concentration of soluble ions decreases as they are precipitated. Note that this process is much more rapid for calcium than for aluminium and the sharp decline in soluble calcium corresponds to gelation. This indication is supported by information from infrared spectroscopy which showed that gelation (initial set) was caused by the precipitation of calcium polyacrylate. This finding was later confirmed by Nicholson et al. (1988b) who, using Fourier transform infrared spectroscopy (FTIR), found that calcium polyacrylate could be detected in the cement paste within one minute of mixing the cement. There was no evidence for the formation of any aluminium polyacrylate within nine minutes and substantial amounts are not formed for about one hour (Crisp et al, 1974).
There is little information available on their setting and structure. Bagby Greener (1985) used Fourier transform infrared spectroscopy (FTIR) to examine the cement-forming reaction between zinc oxide and a mixture of EBA and n-hexyl vanillate. Although they found evidence for reaction between zinc oxide and EBA, they were unable to find any for reaction between zinc oxide and n-hexyl vanillate because of peak overlaps, the minor concentration of n-hexyl vanillate and the subtle nature of the spectral changes. [Pg.343]

In recent years, infrared spectroscopy has been enhanced by the possibility of applying Fourier transform techniques to it. This improved spectroscopic technique, known as Fourier transform infrared spectroscopy (FTIR), is of much greater sensitivity than conventional dispersive IR spectroscopy (Skoog West, 1980). Moreover, use of the Fourier transform technique enables spectra to be recorded extremely rapidly, with scan times of only 0-2 s. Thus it is possible to record spectra of AB cements as they set. By comparison, conventional dispersive IR spectroscopy requires long scan times for each spectrum, and hence is essentially restricted to examining fully-set cements. [Pg.364]

In contrast, SIMCA uses principal components analysis to model object classes in the reduced number of dimensions. It calculates multidimensional boxes of varying size and shape to represent the class categories. Unknown samples are classified according to their Euclidean space proximity to the nearest multidimensional box. Kansiz et al. used both KNN and SIMCA for classification of cyanobacteria based on Fourier transform infrared spectroscopy (FTIR).44... [Pg.113]

Gas chromatography (GC) and with mass spectrometry (GC-MS) Fourier transform infrared spectroscopy (FTIR)... [Pg.564]

Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance spectroscopy ( ll NMR) have become standards for verifying the chemistry of polyanhydrides. The reader is referred to the synthesis literature in the previous section for spectra of specific polymers. The FTIR spectrum for PSA is shown in Fig. 2. In FTIR the absorption... [Pg.189]

Polymerization Behavior. Both Fourier-transform infrared spectroscopy (FTIR) and differential scanning photocalorimetry (DPC) were used to characterize the polymerization behavior, curing time, and maximum double bond conversion in these systems. [Pg.192]

Miniaturized chemical analysis systems have been developed for most macroscopic counterparts (Dittrich et al. 2006). The availability of optical fibers, light sources, and detectors in the visible UV and near-infrared (NIR) wavelengths makes it possible to integrate spectroscopic measurements in microreactors (Lobbecke et al. 2005). Fourier transform infrared spectroscopy (FTIR) is an efficient, broadly applicable... [Pg.68]

Fourier transformed infrared spectroscopy(FTIR) Parkin-aim 6X2000 Surface chemis y, adsorbed species, reaction mechanism Trained Free... [Pg.354]

The 11 nm-sized Ti02 were crystallized using either hydrothermal or thermal methods from 100 nm, amorphous gel spheres. The Ti02 crystal and agglomerate sizes were determined by X-ray diffraction (Philip 1080) and transmission electron microscopy (JEOL JEM 2010), respectively. The surface area and chemistry of the nanostructured Ti02 were analyzed by nitrogen physisorption (Coulter SA 3100) and Fourier transform infrared spectroscopy (FTIR, Perkin-Elmer GX 2000). Metal catalyst was deposited by incipient... [Pg.375]

Fourier transform infrared spectroscopy (FTIR) can now be combined with GC to provide IR spectra on peaks eluting from a capillary column [700-702]. [Pg.88]

The characterization of graphene often involves several techniques in conjunction in order to build up a complete picture of the material. The techniques typically include electron microscopy, Raman spectroscopy, X-ray photo-emission spectroscopy (XPS), Fourier-transform infrared spectroscopy (FTIR) and thermal-gravimetric analysis (TGA). [Pg.33]

One of the initial spectroscopic methods applied to stationary-phase characterization was Fourier transform infrared spectroscopy (FTIR). This originated from several important studies of phase conformational order in crystalline n-alkanes conducted in the late 1960s and early 1980s by Snyder, Maroncelli, and coworkers [111-114], In this work, assignments of C—H bond wagging modes were associated with chain... [Pg.261]

Fourier transform Infrared spectroscopy has been shown to be an excellent tool for surface and Interface studies (.2), In this paper, the application of reflection/absorption Fourier transform Infrared spectroscopy (FTIR-RA) for studying the degradation of amine-cured epoxy and polybutadiene coatings on cold-rolled steel after exposure to a warm, humid environment is reported. [Pg.101]


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