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Integration line

NMR spectroscopy is a quantitative technique and NMR spectra are usually recorded with an integral which indicates the relative areas of the absorption peaks in the spectrum. The area of a peak is proportional to the number of protons which give rise to the signal. In most NMR spectrometers, the integral is represented as a horizontal line plotted over the spectrum. Whenever a peak is encountered, the vertical displacement of the integral line is proportional to the area of the peak. [Pg.38]

Figure 17-6 Proton nmr spectrum of C,0H10Oa at 60 MHz with tetra-methylsilane as the standard. The integral of the offset peak at 16.1 ppm has the same vertical scale as the other integral lines, See Exercise 17-47. Figure 17-6 Proton nmr spectrum of C,0H10Oa at 60 MHz with tetra-methylsilane as the standard. The integral of the offset peak at 16.1 ppm has the same vertical scale as the other integral lines, See Exercise 17-47.
By taking the ratio of both expressions, one obtains a formula, which in the case of an ionizing plasma couples the particle flux to the spatially integrated line emission from that element, provided that the ratio (u ve)/(<7EXgwe) is not strongly temperature or density dependent ... [Pg.139]

Carbon-13 NMR Spectroscopy. High resolution 13C NMR spectra of maltenes, bitumen, and liquid products taken up in a 1 2 mixture of CDC13 were obtained on a Varian XL-100-15 FT spectrometer equipped with a V-4412 probe and a 2.5 mega word disc. A pulse angle of 45° and a repetition period of 60 s were selected to avoid saturation of any nonprotonated carbons. Gated decoupling was also employed to suppress NOE effects in the line intensities. These precautions have been shown for mixtures of model compounds to minimize error in integrated line intensities to less than 10% (3). [Pg.219]

The orientational contribution can be computed directly from the integrated line intensity of the absorption band associated with the dispersion by using the Kramers-Kronig relation in the form... [Pg.250]

The area of each fjeak gives the relative number of protons and is produced directly on the spectrum (Fig. 29.6). On CW—NMR spectrometers the height of the peak area integration line must be measured using a ruler, whereas on FT-NMR machines the area is calculated and displayed as a number. You must remember that ... [Pg.194]

Isolators are now used in industrial scale aseptic processing for both formulation and filling. Fig. 5 shows an example of a rigid interconnected network of isolators providing a complete component handling and aseptic filling capability in an integrated line. The internal... [Pg.2136]

XRD is widely used to determine the degree of crystallinity of pharmaceuticals. The procedure developed by Hermans and Weidinger is based on three assumptions. First, it must be possible to demarcate and measure the crystalline intensity (/J and amorphous intensity (4) from the powder pattern. Usually, the integrated line intensity (area under the curve), rather than the peak intensity (peak height), is measured. Second, there is a proportionality between the experimentally measured crystalline intensity and the crystalline fraction (xc) in the sample. Finally, a proportionality exists between the experimentally measured amorphous intensity and the amorphous fraction (x ) in the sample. The degree of crystallinity (or percent crystallinity), is given by the expression. [Pg.4108]

When measuring intensity, the integrated line intensity (peak area) and not the maximum intensity (peak height) must be measured. Variations in lattice strain and particle size can significantly influence the line shape, but their effect on the integrated intensity will generally be minimal. [Pg.4115]

Use baseline corrections on each integral cut if spectral tilt is noticeable. Extensive zero filling (see step 2) is useful, because it provides more data points to define line shapes better (Section 2-5b). Slight line broadening produces smoother spectral and integral lines with less baseline noise. [Pg.58]

Since LINEs do not contain LTRs, their mechanism of transposition through an RNA Intermediate differs from that of LTR retrotransposons. ORFl and ORF2 proteins are translated from a LINE RNA. In vitro studies Indicate that transcription by RNA polymerase II Is directed by promoter sequences at the left end of Integrated LINE DNA. LINE RNA Is polyadenylated by the same post-transcriptlonal mechanism that polyadenylates other mRNAs. The LINE RNA then Is transported Into the cytoplasm, where It Is translated Into ORFl and ORF2 proteins. Multiple copies of ORFl protein then bind to the LINE RNA, and ORF2 protein binds to the poly (A) tall. [Pg.420]

The extraction of temperatures from SpRS spectra can happen by following a number of different strategies. One is based on the deduction of the number density of all the main molecular species resident in the interaction volume and responsible for rovibrational lines or pure rotational spectra. Another strategy focuses on the details of the whole spectral shape that usually contains a considerable number of lines. Finally, a third approach is rooted in the ratio of integrated line intensities of Stokes and anti-Stokes transitions. [Pg.284]

Analysis of the integration line in the NMR spectrum of 1-bromo-2,2-dimethylpropane. [Pg.539]

Chemical shift (8). The alteration of the resonant frequency of chemically distinct NMR-active nuclei due to the resistance of the electron cloud to the applied magnetic field. The point at which the integral line of a resonance rises to 50% of its total value. [Pg.13]


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See also in sourсe #XX -- [ Pg.361 ]




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Line integrals

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