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Wavelengths function

The software for generation of the channnel to wavelength function is included in the PARC OMA II system. [Pg.39]

The influence of monochromaticity of the incident radiation beam in turbidimetry is not as critical as in spectrophotometry because scattering is involved. Linearity of the analytical response curve is generally not influenced by the spectral bandwidth of the incident beam in a significant manner because the turbidance versus wavelength function is characterised by broader bands. Consequently, relatively large wavelength bandwidths (typically 10—100 nm) can be used. This favours the exploitation of LED-based technology [53]. [Pg.111]

The spectrum of the secondary emission, that is, the intensity of X-ray radiation as a function of wavelength is established using a crystal analyzer based on Bragg s law. [Pg.33]

The first requirement is a source of infrared radiation that emits all frequencies of the spectral range being studied. This polychromatic beam is analyzed by a monochromator, formerly a system of prisms, today diffraction gratings. The movement of the monochromator causes the spectrum from the source to scan across an exit slit onto the detector. This kind of spectrometer in which the range of wavelengths is swept as a function of time and monochromator movement is called the dispersive type. [Pg.57]

SASW-result (dispersion curve) showing Rayleigh Wave speed as a function of wavelength (depth)... [Pg.1005]

The detailed examination of the behavior of light passing through or reflected by an interface can, in principle, allow the determination of the monolayer thickness, its index of refiraction and absorption coefficient as a function of wavelength. The subjects of ellipsometry, spectroscopy, and x-ray reflection deal with this goal we sketch these techniques here. [Pg.126]

In absorption spectroscopy, the attenuation of light as it passes tln-ough a sample is measured as a function of wavelength. The attenuation is due to rovibrational or electronic transitions occurring in the sample. Mapping out the attenuation versus photon frequency gives a description of the molecule or molecules responsible for the absorption. The attenuation at a particular frequency follows the Beer-Lambert law,... [Pg.805]

An illustrative example generates a 2 x 2 calibration matrix from which we can determine the concentrations xi and X2 of dichromate and permanganate ions simultaneously by making spectrophotometric measurements yi and j2 at different wavelengths on an aqueous mixture of the unknowns. The advantage of this simple two-component analytical problem in 3-space is that one can envision the plane representing absorbance A as a linear function of two concentration variables A =f xuX2). [Pg.83]

Measurements were performed employing a Perkin Elmer X2, 5 or 12 UV-Vis spectrophotometer at 25 O.r- C. Equilibrium constants were determined by measuring the extinction coefficient at a suitable wavelength of the partially complexed dienophile (y,.hs) as a function of the concentration of... [Pg.67]

Another related issue is the computation of the intensities of the peaks in the spectrum. Peak intensities depend on the probability that a particular wavelength photon will be absorbed or Raman-scattered. These probabilities can be computed from the wave function by computing the transition dipole moments. This gives relative peak intensities since the calculation does not include the density of the substance. Some types of transitions turn out to have a zero probability due to the molecules symmetry or the spin of the electrons. This is where spectroscopic selection rules come from. Ah initio methods are the preferred way of computing intensities. Although intensities can be computed using semiempirical methods, they tend to give rather poor accuracy results for many chemical systems. [Pg.95]

The specific bonds or functional groups in a molecule responsible for the absorption of a particular wavelength of light... [Pg.382]

Four types of transitions between quantized energy levels account for molecular UV/Vis spectra. The approximate wavelength ranges for these absorptions, as well as a partial list of bonds, functional groups, or molecules that give rise to these transitions is shown in Table 10.5. Of these transitions, the most important are the n and TZ —> TZ, because they involve functional groups that are characteristic... [Pg.382]

In an emission spectrum a fixed wavelength is used to excite the molecules, and the intensity of emitted radiation is monitored as a function of wavelength. Although a molecule has only a single excitation spectrum, it has two emission spectra, one for fluorescence and one for phosphorescence. The corresponding emission spectra for the hypothetical system in Figure 10.43 are shown in Figure 10.44. [Pg.427]

A fluorescence or phosphorescence spectrum in which the emission intensity at a fixed wavelength is measured as a function of the wavelength used for excitation. [Pg.427]


See other pages where Wavelengths function is mentioned: [Pg.171]    [Pg.114]    [Pg.445]    [Pg.178]    [Pg.329]    [Pg.528]    [Pg.22]    [Pg.171]    [Pg.114]    [Pg.445]    [Pg.178]    [Pg.329]    [Pg.528]    [Pg.22]    [Pg.100]    [Pg.100]    [Pg.54]    [Pg.158]    [Pg.717]    [Pg.729]    [Pg.208]    [Pg.875]    [Pg.1121]    [Pg.1125]    [Pg.1734]    [Pg.1974]    [Pg.2420]    [Pg.2871]    [Pg.2949]    [Pg.156]    [Pg.54]    [Pg.3]    [Pg.53]    [Pg.1296]    [Pg.375]    [Pg.378]    [Pg.382]    [Pg.401]    [Pg.406]    [Pg.426]    [Pg.427]    [Pg.432]   


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Function of excitation wavelength

Optical properties solids, as function of wavelength

Quantum Yield a as Function of the Wavelength

Significance of the Peak Absorption Coefficient Functions for Quantitative Millimetre Wavelength Spectrometry

Wave function Wavelength

Wavelength dispersion function

Wavelength selection optimization functions

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