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Spectroscopy derivative, FTIR

In conclusion, the analysis of spectra properly recorded to 185 nm, or lower where possible, can give useful estimates of secondary structure content, but the content of turns and of P-structure should be interpreted with caution. Fourier transform infrared spectroscopy (FTIR) provides better estimates of the latter. When using the results of far-UV CD determination to characterize reproducibility of folding for different samples, it is important first to compare the spectra visually and to look for possible trends or factors that may explain small differences, rather than to rely solely on comparison of derived secondary structure contents. [Pg.239]

The samples of free lipase, pure silica (PS), silanized and activated silica, and immobilized derivatives were submitted to the Fourier Transform Infrared Spectroscopy (FTIR) analysis (Spectrophotometer FTIR BOMEM MB-100). The spectra were obtained in the wavelength range of 400-4000 cm-1 for evaluation of the immobilization procedures. [Pg.311]

Conversion of the as-deposited film into the crystalline state has been carried out by a variety of methods. The most typical approach is a two-step heat treatment process involving separate low-temperature pyrolysis ( 300 to 350°C) and high-temperature ( 550 to 750°C) crystallization anneals. The times and temperatures utilized depend upon precursor chemistry, film composition, and layer thickness. At the laboratory scale, the pyrolysis step is most often carried out by simply placing the film on a hot plate that has been preset to the desired temperature. Nearly always, pyrolysis conditions are chosen based on the thermal decomposition behavior of powders derived from the same solution chemistry. Thermal gravimetric analysis (TGA) is normally employed for these studies, and while this approach seems less than ideal, it has proved reasonably effective. A few investigators have studied organic pyrolysis in thin films by Fourier transform infrared spectroscopy (FTIR) using reflectance techniques. - This approach allows for an in situ determination of film pyrolysis behavior. [Pg.539]

Figures 8B and 8C illustrate the use of second-derivative spectroscopy and FSD, respectively, to resolve the overlapping component bands of the amide I band profile in the FTIR spectrum of p-lactoglobuhn (Figure 8A). Both of these techniques should only be applied to spectra that exhibit a high signal-to-noise ratio (>1000 1), or otherwise artefacts may be introduced by resolution enhancement. The presence of water vapour in the region of the spectrum of interest will also produce features in the processed spectrum that may be misinterpreted as absorption bands of the sample (Figure 9). Figures 8B and 8C illustrate the use of second-derivative spectroscopy and FSD, respectively, to resolve the overlapping component bands of the amide I band profile in the FTIR spectrum of p-lactoglobuhn (Figure 8A). Both of these techniques should only be applied to spectra that exhibit a high signal-to-noise ratio (>1000 1), or otherwise artefacts may be introduced by resolution enhancement. The presence of water vapour in the region of the spectrum of interest will also produce features in the processed spectrum that may be misinterpreted as absorption bands of the sample (Figure 9).
Fourier Transform Infrared Spectroscopy (FTIR) provided a convenient tool by which reaction success was qualitatively evaluated. The spectrum of unfunctionalized PVBC on the polyethylene support is included in Figure 6a. Because of the intense absorbances of the PA, MPE, and IPE species, FTIR proved to be a convenient tool to investigate the progression of the syntheses. Note the changes in the spectra as the membranes were functionalized especially in the range of 900-1250 wavenumber for the MPE and IPE functional groups The PA functionalized membranes have several other very broad characteristic absorbances Figures 6b, 6c, and 6d contain the FTIR spectra of the membranes functionalized with the phosphorous species. Note that the intense absorbances around 3000 wavenumber are derived from the polyethylene support. [Pg.103]

Any technique for gas analysis can be applied to EGA. The most frequently used methods are mass spectroscopy (MS) and Fourier transform infrared spectroscopy (FTIR). Many instrument manufacturers provide the ability to interface their TGAs with MS or FTIR (see Section 3.7, on instrumentation). Temporal resolution between the TGA and the MS or FTIR detector is an important feature, for example, in distinguishing absorbed water from water as a reaction product and in assigning a decomposition product to a specific mass loss. Each method has its experimental requirements, limitations, and advantages. Mass spectroscopy is a very sensitive technique that identifies volatile species by their mass-to-charge ratio, referred to as m/z. The evolution of the sum of all mJz species can be plotted and compared with the derivative TGA plot to ensure temporal resolution between the TGA and the mass spectrometer. The evolution of a specific mJz, associated with species such as water or formaldehyde, can show the distinct evolution of these compounds. The most common ionization is by 70eV electron impact (El), which operates... [Pg.249]

The results of fourier transform-infrared spectroscopy (FTIR) agreed with those of XDR analyses. The solution B-derived film showed an absorption peak due to Zn-O bond vibration around 400 cm when heat-treated at 300° C, while the solution C-and D-derived films showed the absorption at 200°C. In the TGA-DTA curves, a large exothermic peak with large weight loss was found at about 460° C for solution A, about 510°C for solution B, about 390°C for solution C, about 340°C and 400°C for solution D. These results indicate the difference in temperatures for the burning of the organics. [Pg.66]

Pieniazek PA, Stangret J (2005) Hydration of tetraethylammonium tetrafluoroborate derived from FTIR spectroscopy. Vib Spectrosc 39(l) 81-87. doi 10.1016/j.vibspec.2004.11.004... [Pg.68]

The reaction of OH with Af,Af-dimethylformamide has been studied by Solignac et al. (2005) using a relative rate method in combination with long path Fourier transform infrared spectroscopy (FTIR) and gas chromatography (GC). Six different reference compounds were used to derive the rate coefficient values (table VIII-B-3). An unweighted mean of the six values obtained gives k= 1.4 x 10 cm molecule" s at 298 K with an estimated uncertainty of 30%. [Pg.888]

Fourier transform infrared (FTIR) spectroscopy was performed oj a Nicolet 10DX spectrometer. Nuclear magnetic resonance ( H) characterization was accomplished using an IBM 270 SL. Both techniques can successfully be utilized to analyze both the diblock precursors as well as the derived acid containing polymers. [Pg.263]

Derivatives of spectra (dT/dA or dA/dA, and their wavenumber equivalents in FTIR) have been known and used in spectroscopy for a long time. Both first derivatives and second derivatives (d2T/dA2 or d2A/dA2) are in common use in modern spectroscopy, particularly in NIR spectroscopy. We also note that they also enjoy widespread use in some nonoptical spectroscopic techniques, such as NMR and ESR spectroscopies. The mathematics and behavior of the derivative is independent of the particular spectroscopic technique to which it is applied, however. But since our own backgrounds are in optical spectroscopy, where pertinent we will discuss it in terms of the spectroscopy we are familiar with. [Pg.339]


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Derivative spectroscopy

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