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Atomic resonance absorption spectrometry

Bromine-atom atomic resonance absorption spectrometry (ARAS) has been applied to measure the thermal decomposition rate constants of CF3Br in Kr over the temperature range 1222-1624 K. The results were found to be consistent with recently published theory. The formation of cyclopent[a]indene and acenaphthylene from alkyl esters of biphenyl-mono- and -di-carboxylic acids has been observed in flash vacuum pyrolyses at 1000-1100 °C. The kinetics and mechanisms of free-radical generation in the ternary system containing styrene epoxide, / -TsOH, and i-PrOH have been examined in both the presence and absence of O2. ... [Pg.130]

Above 1000 K, the CgHs + O2 C6H5O2 equilibrium will favour CgHs radicals which will then disappear in radical-radical processes or decompose. Stock tube studies [118] using atomic resonance absorption spectrometry to measure [H] provided strong evidence that the phenyl radical... [Pg.117]

A. Lifshitz and M. Frenklach, The reaction between H2 and D2 in a shock tube Study of the atomic VS. molecular mechanism by atomic resonance absorption spectrometry, J. Chem. Phys. 67 ... [Pg.660]

Spectral overlap of emission and absorption wavelengths Is a potential cause of Interference In atomic absorption spectrometry (57) Thus, (a) the emission line of Fe at 352.424 nm Is close to the resonance line of N1 at 352.454, (b) the emission line of Sb at 217.023 nm Is close to the resonance line of Pb at 216.999 nm, and (c) the emission line of As at 228.812 nm Is close to the resonance line of Cd at 228.802 (57). To date, these practically coincident spectral lines have not been reported to be of practical Importance as sources of analytical Interference In atomic absorption analyses of biological materials. [Pg.258]

The basic instrumentation used for spectrometric measurements has already been described in Chapter 7 (p. 277). The natures of sources, monochromators, detectors, and sample cells required for molecular absorption techniques are summarized in Table 9.1. The principal difference between instrumentation for atomic emission and molecular absorption spectrometry is in the need for a separate source of radiation for the latter. In the infrared, visible and ultraviolet regions, white sources are used, i.e. the energy or frequency range of the source covers most or all of the relevant portion of the spectrum. In contrast, nuclear magnetic resonance spectrometers employ a narrow waveband radio-frequency transmitter, a tuned detector and no monochromator. [Pg.355]

Atomic absorption spectrometry (AA). This is a standard laboratory analytical tool for metals. The metal is extracted into a solution and then vaporized in a flame. A light beam with a wavelength absorbed by the metal of interest passes through the vaporized sample for example, to measure zinc, a zinc resonance lamp can be used so that the emission and absorbing wavelengths are perfectly matched. The absorption of the light by the sample is measured and Beer s law is applied to quantify the amount present. [Pg.620]

The techniques considered in this chapter are infrared spectroscopy (or vibrational spectroscopy), nuclear magnetic resonance spectroscopy, ultraviolet-visible spectroscopy (or electronic spectroscopy) and mass spectrometry. Absorption of infrared radiation is associated with the energy differences between vibrational states of molecules nuclear magnetic resonance absorption is associated with changes in the orientation of atomic nuclei in an applied magnetic field absorption of ultraviolet and visible radiation is associated with changes in the energy states of the valence electrons of molecules and mass spectrometry is concerned... [Pg.254]

Before describing the application of Nuclear magnetic resonance (NMR) spectroscopy to potentized homeopathic drugs we would first discuss the basic principles of NMR spectroscopy. This spectroscopy is a powerful tool providing structural information about molecules. Like UV-visible and infra red spectrometry, NMR spectrometry is also a form of absorption spectrometry. Nuclei of some isotopes possess a mechanical spin and the total angular momentum depends on the nuclear spin, or spin number 1. The numerical value of I is related to the mass number and the atomic number and may be 0, Vi, 1 etc. The medium of homeopathic... [Pg.40]

FIGURE 4.4 Assays commonly used in ion channel research. FRET = fluorescence resonance energy transfer Im = transmembrane current Vm = transmembrane potential AVm = change in transmembrane potential A mn = change in concentration of intracellular ion AAS = atomic absorption spectrometry. [Pg.71]

Graphite Furnace Atomic Absorption Spectrometry GF A AS is based on absorption by free atoms, of the resonance lines characteristic of a given element, emitted by the radiation source [6, 72]. [Pg.208]

Thus, the emitting and absorbing atoms have to be embedded in solids and both have to be kept at low temperatures, in order to measure recoilless resonance absorption of y rays. These are essential conditions for Mossbauer spectrometry. [Pg.197]

The application of atomic absorption spectrometry to quantitative analysis is illustrated in Figure 2.2. The incident radiation at resonance wavelength with intensity /q is focused on the flame containing the atoms in their fundamental state and is transmitted with a reduced intensity I determined by the concentration of the atoms in the flame. The radiation is directed to the detector where the intensity is measured. The quantity of absorbed light is determined by comparing / to /q. [Pg.40]

Several physical methods have been employed to ascertain the existence and nature of ICs infrared (IR) absorption spectroscopy nuclear magnetic resonance (NMR) spectroscopy,14 including JH nuclear Overhauser effect (NOE) difference spectroscopy, H 2-D rotating-frame Overhauser effect spectroscopy (2-D ROESY),15 and solid-state 13C cross-polarization/magic angle spinning (CP/MAS) spectroscopy 16 induced circular dichroism (ICD) absorption spectroscopy 17 powder and singlecrystal X-ray diffraction 18 and fast atom bombardment mass spectrometry (FAB MS). [Pg.217]

In atomic absorption spectrometry we need a primary source delivering monochromatic radiation of which the wavelength agrees with that of a resonance line of the elment to be determined. The spectral width must be narrow with respect to the absorption profile of the analyte line. From this point of view atomic absorption... [Pg.32]

Sensitivity is a term used in atomic absorption spectrometry to indicate the concentration that will cause an absorption of 1% (= 0.0044 absorbance units) of the hollow cathode resonance line radiation used for the determination. An example of typical instrumental sensitivity and detection limits for commercially available instruments is given in Table 4.3. [Pg.75]


See other pages where Atomic resonance absorption spectrometry is mentioned: [Pg.246]    [Pg.258]    [Pg.23]    [Pg.8]    [Pg.362]    [Pg.157]    [Pg.335]    [Pg.28]    [Pg.6]    [Pg.2]    [Pg.338]    [Pg.148]    [Pg.250]    [Pg.83]    [Pg.11]    [Pg.1558]    [Pg.857]    [Pg.7]    [Pg.545]    [Pg.138]   


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