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Conversion factors spectrum

For a comparison of experimental Mossbauer isomer shifts, the values have to be referenced to a common standard. According to (4.23), the results of a measurement depend on the type of source material, for example, Co diffused into rhodium, palladium, platinum, or other metals. For Fe Mossbauer spectroscopy, the spectrometer is usually calibrated by using the known absorption spectrum of metallic iron (a-phase). Therefore, Fe isomer shifts are commonly reported relative to the centroid of the magnetically split spectrum of a-iron (Sect. 3.1.3). Conversion factors for sodium nitroprusside dihydrate, Na2[Fe(CN)5N0]-2H20, or sodium ferrocyanide, Na4[Fe(CN)]6, which have also been used as reference materials, are found in Table 3.1. Reference materials for other isotopes are given in Table 1.3 of [18] in Chap. 1. [Pg.81]

Collecting the numerical constants and length conversion factors, we obtain the practical expression Equation 2.37. The proportionality constant will differ for a different choice of units. It is unnecessary and not recommended to convert the emission spectrum of the donor to a wavenumber scale for the calculation of J (see Section 3.4). [Pg.51]

DRS, the method of subtraction of the baseline requires special attention, especially because instructions in various commercial manuals might lead to erroneous results. The procedure adopted by the author involves (i) digital acquisition and storage of the reflectance spectrum of the white standard, Ro(v) over the range of wavenumbers v (cm1) of interest, where v = MX, X is the wavelength in cm and the conversion factor for the photon energy in... [Pg.209]

In this expression J is dimensionless, the half-life has units of seconds and the twentieth-power term in the numerator is a conversion factor with units of moles/photon. The integral overlap of the lamp emission and the chromophore electronic spectrum, EexZx, defines light absorption in photons mole-1 sec-1. EX is the average extinction coefficient for a given wavelength Interval with Zx equaling the lamp output over this same band. [Pg.273]

The property of a Josephson-junction whereby the frequency of the illuminating radiation is converted into a voltage, with a conversion factor based on fundamental constants, means that it too can be used as a spectrum analyzer well suited to (sub)millimetre lasers [3.16]. [Pg.22]

The band gap of mtile Ti02 is larger as compared to that of WO3 and Fc203. The wide band gap of Ti02 proves to be an obstacle in absorption of visible light and also decreases photoenergy conversion factor to less than 1 % since the UV spectrum is only around 4 % of the whole solar spectrum [18, 20],... [Pg.44]

Direct Photolysis. Direct photochemical reactions are due to absorption of electromagnetic energy by a pollutant. In this "primary" photochemical process, absorption of a photon promotes a molecule from its ground state to an electronically excited state. The excited molecule then either reacts to yield a photoproduct or decays (via fluorescence, phosphorescence, etc.) to its ground state. The efficiency of each of these energy conversion processes is called its "quantum yield" the law of conservation of energy requires that the primary quantum efficiencies sum to 1.0. Photochemical reactivity is thus composed of two factors the absorption spectrum, and the quantum efficiency for photochemical transformations. [Pg.29]

Characterization of the reaction intermediate is facilitated by studies in a flow system in which the sample cell and a reference cell are mounted in series in a double beam spectrometer (IS). Not only can we observe the intermediate bands under rigorous steady state conditions, but we can monitor the conversion by sampling the effluent. In addition, the reference cell assures the spectrum we see is that of surface species. Primitive analysis of the kinetics reveals the intermediate is favored by relatively high ethylene pressures hence, use of a reference cell to cancel contributions of the gas phase is an important factor. [Pg.23]

Currently used nonlinear optical crystals are potassium dihydrogen phosphate (KDP) and barium borate (BBO). Compared to KDP, the advantages of BBO are its transparency in the UV and its larger quantum efficiency of up-conversion by a factor of 4—6. For a given position of the crystal, only a narrow band of the fluorescence spectrum is up-converted. Therefore, if the full fluorescence spectrum is of interest, the crystal must be rotated at a series of angles. An example of experimental set-up is presented in Figure 11.2. The fwhm of the response is 210 fs. [Pg.352]

Natural minerals may contain simultaneously up to 20-25 luminescence centers, which are characterized by strongly different emission intensities. Usually one or two centers dominate, while others are not detectable by steady-state spectroscopy. In certain cases deconvolution of the liuninescence spectra may be useful, especially in the case of broad emission bands. It was demonstrated that for deconvolution of luminescence bands into individual components, spectra have to be plotted as a function of energy. This conversion needs the transposition of the y-axis by a factor A /hc (Townsend and Rawlands 2000). The intensity is then expressed in arbitrary imits. Deconvolution is made with a least squares fitting algorithm that minimizes the difference between the experimental spectrum and the sum of the Gaussian curves. Based on the presumed band numbers and wavelengths, iterative calculations give the band positions that correspond to the best fit between the spectrum and the sum of calculated bands. The usual procedure is to start with one or... [Pg.38]

The similarity of the absorption spectrum of DMP to that of TMB indicates a similar electronic structure. The structure of TMB is deviated from pseudo-Dsh symmetry because of repulsion of three Me groups, while that of DMP is closer to pseudo-Dsh symmetry. When Dsh symmetry is an important factor for higher efficiency of the fluorescence and Me group enhances internal conversion, DMP fluoresces stronger than TMB . It is interesting to know whether unimolecular deprotonation from DMP " ... [Pg.689]


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See also in sourсe #XX -- [ Pg.66 , Pg.67 , Pg.68 ]




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