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Fourier transform infrared spectroscopy definition

CO adsorption on Cu electrode surface is interfered with by specifically adsorbed anions. CO can be adsorbed below a certain definite potential, determined by the adsorption strength of CO and the anion. When CO molecules displace the specifically adsorbed anions on Cu electrode, a voltammetric peak is observed as exemplified for Cu(lOO) in CO saturated phosphate buffer solution in comparison with N2 saturated solution (Fig. 29). Subtractively normalized interfacial Fourier transform infrared spectroscopy (SNIFTIRS) spectra in Fig. 30 demonstrates that CO is adsorbed at -0.8 V vs. SHE but not at -0.4 V, and adsorbed phosphate anion vice versa. " This process is equivalent to charge displacement adsorption of CO on Pt electrode revealed by Clavilier et al The profile of the voltammogram depends greatly on the crystal... [Pg.170]

The selective detectors discussed in the previous sections often do not provide enough information to elucidate with 100% probability the nature of the eluting solutes. For this reason, data with selective detectors can be erratic. The future in this respect definitely belongs to the spectroscopic detectors that allow. selective recognition of the separated compounds. Today, the hyphenated techniques CGC-mass spectroscopy (CGC-MS), CGC-Fourier transform infrared spectroscopy (CGC-FTIR), and CGC-atomic emission detection (CGC - AED) are the most powerful analytical techniques available. They provide sensitive and selective quantitation of target compounds and structural elucidation or identification of unknowns. The applicability and ease of use of the hyphenated techniques were greatly increased by the introduction of fused silica wall coaled open tubular columns. The main reason for this is that because of the low flows of capillary columns, no special interfaces are required and columns are connected directly to the different spectrometers. The introduction of relatively inexpensive benchtop hyphenated systems has enabled many laboratories to acquire such instrumentation, which in turn has expanded their applicability ever further. [Pg.236]

Figure 11 IR difference spectra, CZ-FZ, using FZ (bottom) as reference. Samples were 2 mm thick. Carbon-oxygen complex bands are indicated by arrows. See text for definition of CZ and FZ. Reproduced by permission of Academic Press from Krishnan K, Stout PJ and Watanabe M (1990) Characterisation of semiconductor silicon using Fourier transform infrared spectrometry. In Ferraro JR and Krishnan K (eds) Practical Fourier Transform Infrared Spectroscopy, pp 286-351. New York Academic Press. Figure 11 IR difference spectra, CZ-FZ, using FZ (bottom) as reference. Samples were 2 mm thick. Carbon-oxygen complex bands are indicated by arrows. See text for definition of CZ and FZ. Reproduced by permission of Academic Press from Krishnan K, Stout PJ and Watanabe M (1990) Characterisation of semiconductor silicon using Fourier transform infrared spectrometry. In Ferraro JR and Krishnan K (eds) Practical Fourier Transform Infrared Spectroscopy, pp 286-351. New York Academic Press.
Spectroscopy. Infrared spectroscopy (48) permits stmctural definition, eg, it resolves the 2,2 - from the 2,4 -methylene units in novolak resins. However, the broad bands and severely overlapping peaks present problems. For uncured resins, nmr rather than ir spectroscopy has become the technique of choice for microstmctural information. However, Fourier transform infrared (ftir) gives useful information on curing phenoHcs (49). Nevertheless, ir spectroscopy continues to be used as one of the detectors in the analysis of phenoHcs by gpc. [Pg.299]

It is only since 1980 that in situ spectroscopic techniques have been developed to obtain identification of the adsorbed intermediates and hence of reliable reaction mechanisms. These new infrared spectroscopic in situ techniques, such as electrochemically modulated infrared reflectance spectroscopy (EMIRS), which uses a dispersive spectrometer, Fourier transform infrared reflectance spectroscopy, or a subtractively normalized interfacial Fourier transform infrared reflectance spectroscopy (SNIFTIRS), have provided definitive proof for the presence of strongly adsorbed species (mainly adsorbed carbon monoxide) acting as catalytic poisons. " " Even though this chapter is not devoted to the description of in situ infrared techniques, it is useful to briefly note the advantages and limitations of such spectroscopic methods. [Pg.76]

Because neither PrP" nor PrP " " could be crystallized, it was not possible to establish the 3D structure of these proteins by X-ray crystallography To circumvent this xmfavorable situation, Prusiner used circular dichroism and Fourier transformed infrared (FTIR) spectroscopy, both techniques that allow determination of the respective percentages of the secondary structures (a, (3, and turns) in a peptide or a protein. Applied to PrP and PrP samples, these spectroscopic approaches definitely demonstrated that both isoforms have a distinct 3D structure. In a seminal article published in 1993, the Prusiner s group established that PrP is chiefly an a-helical protein (43% of a-helix structure) with few -structures (3%). In contrast, PrP has less a-helix (30%) but has gained a high percentage of -structures (43%). [Pg.206]

Infrared (in) spectrometers are gaining popularity as detectors for gas chromatographic systems, particularly because the Fourier transform iafrared (ftir) spectrometer allows spectra of the eluting stream to be gathered quickly. Gc/k data are valuable alone and as an adjunct to gc/ms experiments. Gc/k is a definitive tool for identification of isomers (see Infrared and raman spectroscopy). [Pg.108]

Vibrational spectroscopy (particularly infrared) has found wide application in the characterisation of supported metal carbonyl clusters. Such studies have been facilitated by the advent of high-sensitivity Fourier transform instrumentation. However, the information provided should be used with caution — the behaviour of carbonyl stretching vibrations need not necessarily correlate in any definite or specific manner with the presence or absence of metal-metal bonding in a supported organometallic carbonyl species. [Pg.81]


See other pages where Fourier transform infrared spectroscopy definition is mentioned: [Pg.297]    [Pg.131]    [Pg.27]    [Pg.6]    [Pg.368]    [Pg.132]    [Pg.17]    [Pg.468]    [Pg.701]    [Pg.248]    [Pg.93]    [Pg.364]    [Pg.77]    [Pg.217]    [Pg.39]   
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