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Absorbance spectrum for

Now that we have spectra for each of the pure components, we can put the concentration values for each sample into the Beer-Lambert Law to calculate the absorbance spectrum for each sample. But first, let s review various ways of... [Pg.38]

Plots of the correlation coefficients obtained from the absorbance and its first and second derivatives (D1 and D2) are shown superimposed on the absorbance spectrum of the 100% Fe SWy in Figure 4a. Correlation coefficients for the full set, superimposed on the absorbance spectrum for 100% Fe Otay sample, are shown in Figure 4b. The quality of the correlation is significantly improved using 1st derivative data and improved still further using 2nd derivative data. This can be seen from Table III where a summary of the correlation coefficients obtained from absorbance and first and second derivatives of absorbance at several prominent wavelengths, including the computer optimum, are displayed. [Pg.414]

Figure 10. VCD and absorbance spectrum for (+)-limonene measured with a PMI FT-VCD spectrometer. Figure 10. VCD and absorbance spectrum for (+)-limonene measured with a PMI FT-VCD spectrometer.
The aromatic nature of macrocycles 4.96a-4.99 was inferred from the large diamagnetic ring-current effect observed in their H NMR spectra. For instance, in the case of the octaethyl derivative 4.96a, the shift difference between the internal C-H protons and the external ones was found to be 25.3 ppm. This shift difference is over twice as large as that found for [18]annulene (A5 = 12.1 ppm). The UV-vis absorbance spectrum for 4.96a exhibits an intense Soret-like absorbance at 547 nm... [Pg.212]

The concentration of bilirubin in amniotic fluid is generally too low (-0.01 to 0.03mg/dL 0.17 to 0.51pmol/L) to be measured by standard photometric techniques, but the determination can be done rapidly, accurately, and directly by absorption spectrophotometry. The maximal absorbance of bilirubin is at 450 nm. In the absence of significant amounts of bilirubin, the absorbance spectrum for the amniotic fluid between 365 and 550 nm defines a nearly exponential curve (Figure 54-16). On log-linear axes, the height of the curve at 450 nm above the straight line is linearly proportional to the concentration of bilirubin in the... [Pg.2187]

Figure 4 Absorbance spectrum for pyridoxal phosphate, alone and 1n the presence of aminooxy acetate(l), propionate(2), butyrate(3) and valerate(4). Figure 4 Absorbance spectrum for pyridoxal phosphate, alone and 1n the presence of aminooxy acetate(l), propionate(2), butyrate(3) and valerate(4).
Fig. 1. A characteristic absorbance spectrum for seawater (Florida Bay, South Florida) overlaid by a typical sunlight incident spectrmn at the sea siuface at noon (LI-COR radiometer). Bulk natural water sample 10 cm pathlength... Fig. 1. A characteristic absorbance spectrum for seawater (Florida Bay, South Florida) overlaid by a typical sunlight incident spectrmn at the sea siuface at noon (LI-COR radiometer). Bulk natural water sample 10 cm pathlength...
FIGURE 12.5 Detection mechanism. Panel A shows an idealized absorbance spectrum for a porphyrin in solution. When the porphyrin interacts with the immobilized enzyme, the preexposure spectrum is observed (Panel B). Upon exposure of the porphyrin-enzyme surface to the target analyte, the porphyrin dissociates from the enzyme resulting in unique postexposure absorbance spectra depending on whether the sample is applied as a vapor (Panel C) or in solution (Panel D). Difference spectra are calculated as the postexposure absorbance spectrum minus the preexposure absorbance spectrum. The rhombus represents porphyrin, the concave shape represents enzyme, and the black rectangle represents immobilization support. [Pg.321]

Figure 2. In vivo action spectrum for 32K degradation and absorbance spectrum for plastosemiquinone anion radical. The action spectrum for the rate of 32K degradation (histogram) is redrawn from Greenberg et al (20). The absorbance spectrum for plastosemiquinone in alkaline methanol (—) is redrawn from Amesz (28). Figure 2. In vivo action spectrum for 32K degradation and absorbance spectrum for plastosemiquinone anion radical. The action spectrum for the rate of 32K degradation (histogram) is redrawn from Greenberg et al (20). The absorbance spectrum for plastosemiquinone in alkaline methanol (—) is redrawn from Amesz (28).
All polarizers are placed within the sample compartment directly in the infrared beam. They are mounted for complete 360" rotation. At 0° or 180° rotational settings the transmitted electric field vector (E) of the infrared energy is horizontal (s-polarized). This represents the A n or the absorbance spectrum for parallel polarized light. Likewise at 90° or 270° rotational settings the transmitted electric field vector (E) of the infrared energy is vertical (p-polarized). This represents the or the absorbance spectrum for perpendicularly polarized light. [Pg.528]

Fig. 1. Absorbance spectrum for the OB-2 crude oil sample emulsion in the vicinity of the vanadium secondary line at 305.633nm, with a pyrolysis temperature of 1000 °C,... Fig. 1. Absorbance spectrum for the OB-2 crude oil sample emulsion in the vicinity of the vanadium secondary line at 305.633nm, with a pyrolysis temperature of 1000 °C,...
Figure 8.35 Time-resolved absorbance spectrum for DOLT-2 Dogfish Liver reference material in the vicinity of the cobalt absorption line at 240.725 nm (a). solubilized in TMAH (b)... Figure 8.35 Time-resolved absorbance spectrum for DOLT-2 Dogfish Liver reference material in the vicinity of the cobalt absorption line at 240.725 nm (a). solubilized in TMAH (b)...
Figure 8.43 Time-resolved absorbance spectrum for cadmium in SARM-20 coal in the vicinity of 228.802 nm pyrolysis temperature 800 °C, atomization temperature 1700 °C direct solid sample analysis with Ir as permanent modifier... Figure 8.43 Time-resolved absorbance spectrum for cadmium in SARM-20 coal in the vicinity of 228.802 nm pyrolysis temperature 800 °C, atomization temperature 1700 °C direct solid sample analysis with Ir as permanent modifier...

See other pages where Absorbance spectrum for is mentioned: [Pg.7]    [Pg.533]    [Pg.146]    [Pg.119]    [Pg.88]    [Pg.6470]    [Pg.221]    [Pg.221]    [Pg.6469]    [Pg.164]    [Pg.154]    [Pg.61]    [Pg.107]    [Pg.93]    [Pg.172]   
See also in sourсe #XX -- [ Pg.373 , Pg.373 ]




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Absorbance spectrum

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