Peak height

The external reflection of infrared radiation can be used to characterize the thickness and orientation of adsorbates on metal surfaces. Buontempo and Rice [153-155] have recently extended this technique to molecules at dielectric surfaces, including Langmuir monolayers at the air-water interface. Analysis of the dichroic ratio, the ratio of reflectivity parallel to the plane of incidence (p-polarization) to that perpendicular to it (.r-polarization) allows evaluation of the molecular orientation in terms of a tilt angle and rotation around the backbone [153]. An example of the p-polarized reflection spectrum for stearyl alcohol is shown in Fig. IV-13. Unfortunately, quantitative analysis of the experimental measurements of the antisymmetric CH2 stretch for heneicosanol [153,155] stearly alcohol [154] and tetracosanoic [156] monolayers is made difflcult by the scatter in the IR peak heights. 

The correction due to the temperature gradient in the capillary wave peak heights is the corresponding fractional difference, which can be obtained by evaluating A(<7, = w. The result is simple ... 

The peak at mje = 98 is taken as the arbitrary standard. The height of the other peaks is measmed relative to it. Once this matrix has been established, ordered sets of mass spectral peak heights at mfe = 69, 83, 84, and 98 constitute the experimental b vector for an unknown mixture that contains or may contain the four... 

Band Asymmetry. The peak asymmetry factor AF is often defined as the ratio of peak half-widths at 10% of peak height, that is, the ratio b/a, as shown in Fig. 11.2. When the asymmetry ratio lies outside the range 0.95-1.15 for a peak of k =2, the effective plate number should be calculated from the expression... 

Quantitative Calculations In a quantitative analysis, the height or area of an analyte s chromatographic peak is used to determine its concentration. Although peak height is easy to measure, its utility is limited by the inverse relationship between the height and width of a chromatographic peak. Unless chromatographic conditions are carefully controlled to maintain a constant column efficiency, variations in... 

With conventional nonspectroscopic detectors, other methods must be used to identify the solutes. One approach is to spike the sample by adding an aliquot of a suspected analyte and looking for an increase in peak height. Retention times also can be compared with values measured for standards, provided that the operating conditions are identical. Because of the difficulty of exactly matching such conditions, tables of retention times are of limited utility. 

Peak Height Peak Height Miiiigrams Miiiigrams Ratio Ratio... 

After adding a 10.00-mL portion of the internal standard, the solution was filtered. Analysis of the sample gave a peak height ratio of 23.2 for ASA and 17.9 for CAE. 

The analysis of N03 in aquarium water was carried out by CZE using 104 as an internal standard. A standard solution of 15.0-ppm N03 and 10.0-ppm 104 gives peak heights (arbitrary units) of 95.0 and 100.1, respectively. A sample of water from an aquarium is diluted 1 100, and sufficient internal standard added to make its concentration 10.0 ppm. Analysis gives signals of 29.2 and 105.8 for N03 and 104 , respectively. Report the parts per million of N03 in the sample of aquarium water. 

Of the six parameters shown in Figure 13.18, the most important are peak height and return time. The peak height is related, directly or indirectly, to the analyte s concentration and is used for quantitative work. The sensitivity of the method, therefore, is also determined by the peak height. The return time determines the frequency with which samples maybe injected. Figure 13.19 shows that when a second sample is injected at a time T after injecting the first sample. 

Most flow injection analyses use peak height as the analytical signal. When there is insufficient time for reagents to merge with the sample, the result is a split-peak, or doublet, due to reaction at the sample s leading and trailing edges. This experiment describes how the difference between the peak times can be used for quantitative work. 

When a mass spectrum has been acquired by the spectrometer/computer system, it is already in digital form as m/z values versus peak heights (ion abundances), and it is a simple matter for the computer to compare each spectrum in the library with that of the unknown until it finds a match. The shortened search is carried out first, and the computer reports the best fits or matches between the unknown and spectra in the library. A search of even 60,000 to 70,000 spectra takes only a few seconds, particularly if transputers are used, thus saving the operator a great deal of time. Even a partial match can be valuable because, although the required structure may not have been found in the library, it is more than likely that some of the library compounds will have stractural pieces that can be recognized from a partial fit and so provide information on at least part of the structure of the unknown. 

Resolution 10% valley definition, m/Am. Let two peaks of equal height in a mass spectrum at masses m and m/Am be separated by a valley that at its lowest point is just 10% of the height of either peak. For similar peaks at a mass exceeding m, let the height of the valley at its lowest point be more (by any amount) than 10% of either peak height. Then the resolution (10% valley definition) is m/Am. It is usually a function of m therefore, m/Am should be given for a number of values of m. 

Resolving power (mass). The ability to distinguish between ions differing slightly in mass-to-charge ratio. It can be characterized by giving the peak width, measured in mass units, expressed as a function of mass, for at least two points on the peak, specifically for 50% and for 5% of the maximum peak height. 

Because the line width is much less than the resolution this ratio is not reflected in the peak heights in Figure 6.8. 

Transitions. Samples containing 50 mol % tetrafluoroethylene with ca 92% alternation were quenched in ice water or cooled slowly from the melt to minimise or maximize crystallinity, respectively (19). Internal motions were studied by dynamic mechanical and dielectric measurements, and by nuclear magnetic resonance. The dynamic mechanical behavior showed that the CC relaxation occurs at 110°C in the quenched sample in the slowly cooled sample it is shifted to 135°C. The P relaxation appears near —25°C. The y relaxation at — 120°C in the quenched sample is reduced in peak height in the slowly cooled sample and shifted to a slightly higher temperature. The CC and y relaxations reflect motions in the amorphous regions, whereas the P relaxation occurs in the crystalline regions. The y relaxation at — 120°C in dynamic mechanical measurements at 1 H2 appears at —35°C in dielectric measurements at 10 H2. The temperature of the CC relaxation varies from 145°C at 100 H2 to 170°C at 10 H2. In the mechanical measurement, it is 110°C. There is no evidence for relaxation in the dielectric data. 

Fig. 7. Comparison of various transport schemes for advecting a cone-shaped puff in a rotating windfield after one complete rotation (a), the exact solution (b), obtained by an accurate numerical technique (c), the effect of numerical diffusion where the peak height of the cone has been severely tmncated and (d), where the predicted concentration field is very bumpy, showing the effects of artificial dispersion. In the case of (d), spurious waves are...

FIG. 16"31 Properties of a Gaussian peak. is the peak height tfn, the peak apex time <3, the... 

In practice, the calculation of peak skew for highly tailing peaks is rendered difficult by basehne errors in the calculation of third moments. The peak asymmetry factor, A, = b/a, at 10 percent of peak height (see Fig. 16-32) is thus frequently used. An approximate relationship between peak skew and A, for taihng peaks, based on data in Yau et al. is Peak skew= [0.51 -t- 0.19/(A, — 1)] . Values of A, < 1.25... 

FIG. 16-32 Exponentially modified Gaussian peak with Xq/Gq = 1.5. The graph also shows the definition of the peak asymmetry factor at 10 percent of peak height. 

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