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Molar absorption coefficients for

A) The use of a calibration graph. This overcomes any problems created due to non-linear absorbance/concentration features and means that any unknown concentration run under the same conditions as the series of standards can be determined directly from the graph. The procedure requires that all standards and samples are measured in the same fixed-path-length cell, although the dimensions of the cell and the molar absorption coefficient for the chosen absorption band are not needed as these are constant throughout all the measurements. [Pg.753]

The molar-absorption coefficients for such transitions will be very small and so Ti states will have a longer lifetime than Si states. In... [Pg.57]

Alternatively the absorbance of the mixture can be measured at different wavelengths (usually one for each compound present) and, provided that the molar absorption coefficients for each compound at each wavelength are known, the concentration of each compound can be calculated. Procedure 2.2 illustrates such a calculation. [Pg.56]

The enzyme activity in katals per litre may be calculated from the molar absorption coefficient for NADH at 340 nm (6.22 X 103 1 mol-1 cm-1). [Pg.290]

A. The use of the molar absorption coefficient for NADI I to calculate the concentration change (mol... [Pg.290]

Fig. 5. Data for frequency shift, Av monomer frequency minus H-bonded frequency), band width at half maximum iq, and integrated molar absorption coefficient per bonded OH minus integrated molar absorption coefficient for monomer, AB. Curves are those... Fig. 5. Data for frequency shift, Av monomer frequency minus H-bonded frequency), band width at half maximum iq, and integrated molar absorption coefficient per bonded OH minus integrated molar absorption coefficient for monomer, AB. Curves are those...
This weak transition is due to the promotion of an electron from the non-bonding molecular orbital n to an anti-bonding tt orbital. This transition is usually observed in molecules that contain a heteroatom as part of an unsaturated system. The most common of these bands corresponds to the carbonyl band at around 270 to 295 nm, which can be easily observed. The molar absorption coefficient for this band is weak. The nature of the solvent influences the position of absorption bands because the polarity of the bond is modified during absorption. For example, ethanal Amax = 293 nm (e = 12 in ethanol as solvent). [Pg.193]

Calculate the molar absorptivity coefficient for the permanganate at this wavelength. [Pg.218]

The following table gives the absorbances for various concentrations of a solution. A 1 cm optical cell is used. Use this to calculate the molar absorption coefficient for the solute. [Pg.39]

Table 7 Values of Quantum Yields and Molar Absorption Coefficients for Different Water Pollutants and Oxidants in Water... [Pg.32]

Fig. 2 a Molar absorption coefficients for ferric species of interest (Fe3+ and FeOH2+), and b HO quantum yields obtained from photolysis of pH 3 ferric solutions in the wavelength range 280-370 nm in the presence and absence of oxygen (data from [10])... [Pg.259]

An aqueous solution of diazoniun salt and polyvinyl pyrrolidone is used as a contrast enhancement material. An improved resist profile is obtained with this CEL material when a g-line stepper is used. Resist contrast is discussed in terms of such optical characteristics as the quantun yield of bleaching and the molar absorption coefficient for the materials. [Pg.188]

According to Griffing and West, the main requirements for CEL materials are as followsd) (1) the molar absorption coefficient for the photobleachable dye must be as high as possible, (2) the Ta>/Tb ratio must be as large as possible, and (3) the quantun yield of the bleaching reaction must be as high as possible. [Pg.197]

Ae In circular dichroism, amplitude of the CD maximum difference in molar absorption coefficients for right and left circularly polarised light. May be positive or negative. [Pg.157]

The Use of DEC. Detection of Methacrylate (and Acrylate) Component. DCE was transparent at wavelengths over 230 nm, and methacrylate (and acrylate) homopolymers and copolymers could be monitored with a UV detector around 233 nm (9). The molar absorption coefficients for both polystyrene and poly(methyl methacrylate) (PMMA) at 233 nm were nearly equal, and the chromatograms obtained at this wavelength reflected the relative amounts of the copolymers with different chemical compositions. [Pg.220]

DNA fragments separated by polymer networks are detected by ultraviolet (UV) detector or laser-induced fluorescence (LIF) detection. UV detection of DNA fragments is based on the UV absorption of the DNA bases that is, the wavelength and the molar absorption coefficient for the UV absorption maxima of DNA bases are 260 nm for A, 254 nm for G, 267 nm for T, and 271 nm for C, respectively. [Pg.1056]

XH NMR experiments show that the viologen residue interacts effectively with the CB7 host [53], Voltammetric and mass spectrometric data are also consistent with the formation of inclusion complexes between the dendronized viologens and CB7. As was the case with methylviologen, complexation by CB7 depresses the molar absorptivity coefficient for the viologen UV absorption band and this effect can be conveniently utilized to fit the absorbance data in titration experiments to 1 1 binding isotherms. From the optimization of these fittings we obtained the corresponding equilibrium association constants (Table 3). [Pg.224]

Eyer P, Worek F, Kiderlen D, Sinko G, Stuglin A, Simeon-Rudolf V, Reiner E. Molar absorption coefficients for the reduced Ellman reagent reassessment. Anal Biochem, 2003 312 224—227. [Pg.543]

When monochromatic circularly polarized light passes through an enantiomeri-cally pure sample which absorbs at the corresponding frequency, rep light will be absorbed to a greater or less extent than Icp light. The circular dichroism (CD) of the sample is defined as Ae = l — Er where El and are the molar absorption coefficients for Icp and rep light, respectively. [Pg.145]

Recommendations on experimental methods for the determination and the compilation of molar absorption coefficients for transient species in solution have been proposed by Bonneau, Carmichael, and Hug . Note should be taken of the proposals put forward. [Pg.8]

TABLE 4.2 Molar Absorptivity Coefficients for Compounds Formed During the Classical Determinations of Some Metal Ions. X = Wavelength of Maximum Absorption. For Experimental Conditions, see Ref. [13]... [Pg.101]

In very rare cases in which photoionization is the only photoprocess, the absorption observed in a nitrous oxide-saturated solution will be that of the cation radical. However, generally, other processes such as intersystem crossing also occur in parallel. In the presence of oxygen, the hydrated electron and the triplet will be scavenged at diffusion-controlled rates, and the absorption observed in the oxygenated solution will be due to the cation radical. Under these conditions, the cation radical spectrum is easily determined. The molar absorption coefficient of the cation radical can also be calculated using the hydrated electron as an internal standard. The molar absorption coefficient for sulphacetamide cation radical was determined in this manner (Land et al 1982) and later confirmed by pulse radiolysis (see Section 12.2.2.6). [Pg.271]

Photolysis of nitrous oxide at 1470 A. in these solutions can be discounted since the molar absorption coefficient for cyclohexane is 10,000 M"1 cm."1 (10) and that for nitrous oxide about 2500Af"1 cm."1 (13). Preferential absorption by nitrous oxide would occur if nitrous oxide were adsorbed on the sapphire window, but this is discounted since the nitrogen yield is a function of the alkane present. [Pg.488]


See other pages where Molar absorption coefficients for is mentioned: [Pg.671]    [Pg.114]    [Pg.13]    [Pg.49]    [Pg.333]    [Pg.333]    [Pg.28]    [Pg.551]    [Pg.234]    [Pg.160]    [Pg.31]    [Pg.70]    [Pg.115]    [Pg.535]    [Pg.396]    [Pg.323]    [Pg.79]    [Pg.115]    [Pg.239]    [Pg.141]    [Pg.39]    [Pg.360]    [Pg.364]    [Pg.171]    [Pg.58]   


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