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Optical absorption spectroscopy, atomic

In atomic absorption spectroscopy (AAS), the optical absorption of atoms in their ground state is measured when the sample is irradiated with the appropriate source. [Pg.253]

In many synthetically useful radical chain reactions, hydrogen donors are used to trap adduct radicals. Absolute rate constants for the reaction of the resulting hydrogen donor radicals with alkenes have been measured by laser flash photolysis techniques and time-resolved optical absorption spectroscopy for detection of reactant and adduct radicals Addition rates to acrylonitrile and 1,3-pentadienes differ by no more than one order of magnitude, the difference being most sizable for the most nucleophilic radical (Table 8). The reaction is much slower, however, if substituents are present at the terminal diene carbon atoms. This is a general phenomenon known from addition reactions to alkenes, with rate reductions of ca lOO observed at ambient temperature for the introduction of methyl groups at the attacked alkene carbon atom . This steric retardation of the addition process either completely inhibits the chain reaction or leads to the formation of rmwanted products. [Pg.625]

Heavy metals, boron (B(V)), arsenic and total phosphorus were determined in the fraction < 20 pm to improve the comparability of the results. This fraction was separated from the freeze-dried and non-milled samples by ultrasonic sieving (Ackermann 1980). Metals were analysed after microwave-assisted digestion with aqua regia at 180 °C in closed vessels by inductively coupled plasma optical emission spectroscopy, atomic fluorescence spectroscopy (mercury) and hydride atomic absorption spectroscopy (arsenic). [Pg.149]

Cluster properties, mostly those that control electron transfer processes such as the redox potential in solution, are markedly dependent on their nuclearity. Therefore, clusters of the same metal may behave as electron donor or as electron acceptor, depending on their size. Pulse radiolysis associated with time-resolved optical absorption spectroscopy is used to generate isolated metal atoms and to observe transitorily the subsequent clusters of progressive nuclearity yielded by coalescence. Applied to silver clusters, the kinetic study of the competition of coalescence with reactions in the presence of added reactants of variable redox potential allows us to describe the autocatalytic processes of growth or corrosion of the clusters by electron transfer. The results provide the size dependence of the redox potential of some metal clusters. The influence of the environment (surfactant, ligand, or support) and the role of electron relay of metal clusters in electron transfer catalysis are discussed. [Pg.293]

Irradiation by ionizing radiation able to penetrate into a zeolite material exchanged by metal ions allows to generate metal atoms and clusters in situ in the cavities.The observation of irradiated faujasite (Na-Y zeolite) by optical absorption spectroscopy at increasing doses and at low silver content demonstrates the formation of two bands at 265 and 305 nm which have been assigned to the charged trimer Agj ". Then, the ESR observation after a dehydration step indicates the reduction of this species into Agj . Irradiation of HjPtClg solution included in mesoporous channels of molecular sieves induces nanowires of platinum. ... [Pg.433]

H. Edner, P. Ragnarson, S. Spannare, S. Svanberg A differential optical absorption spectroscopy (DOAS) system for urban atmospheric pollution monitoring. Appl. Opt. 32, 327 (1993) and Lund Reports on Atomic Physics LRAP-133 (Lund Institute of Technology, Lund 1992)... [Pg.493]

Detector Detection in FIA may be accomplished using many of the electrochemical and optical detectors used in ITPLC. These detectors were discussed in Chapter 12 and are not considered further in this section. In addition, FIA detectors also have been designed around the use of ion-selective electrodes and atomic absorption spectroscopy. [Pg.652]

Analyses of alloys or ores for hafnium by plasma emission atomic absorption spectroscopy, optical emission spectroscopy (qv), mass spectrometry (qv), x-ray spectroscopy (see X-ray technology), and neutron activation are possible without prior separation of hafnium (19). Alternatively, the combined hafnium and zirconium content can be separated from the sample by fusing the sample with sodium hydroxide, separating silica if present, and precipitating with mandelic acid from a dilute hydrochloric acid solution (20). The precipitate is ignited to oxide which is analy2ed by x-ray or emission spectroscopy to determine the relative proportion of each oxide. [Pg.443]

Aluminum is best detected quaUtatively by optical emission spectroscopy. SoHds can be vaporized direcdy in a d-c arc and solutions can be dried on a carbon electrode. Alternatively, aluminum can be detected by plasma emission spectroscopy using an inductively coupled argon plasma or a d-c plasma. Atomic absorption using an aluminum hoUow cathode lamp is also an unambiguous and sensitive quaUtative method for determining alurninum. [Pg.105]

Ozin, Hanlan, and Power, using optical spectroscopy (49,121). In view of the marked temperature-effect observed for the cobalt system, we shall focus on this cluster system here. Evidence for cobalt-atom aggregation at the few-atom extreme first came from a comparison of the optical data for Co Ar — 1 10 mixtures recorded at 4.2 and 12 K (see Fig. 4). A differential of roughly 8 K in this cryogenic-temperature regime was sufficient to cause the dramatic appearance of an entirely new set of optical absorptions in the regions 320-340 and 270-280 nm (see Fig. 4). Matrix variation, from Ar, to Kr, to Xe, helped clarify atom-cluster, band-overlap problems (see Fig. 5). [Pg.87]

The optical absorption spectra of sulfonyl radicals have been measured by using modulation spectroscopy s, flash photolysis and pulse radiolysis s techniques. These spectra show broad absorption bands in the 280-600 nm region, with well-defined maxima at ca. 340 nm. All the available data are summarized in Table 3. Multiple Scattering X, calculations s successfully reproduce the experimental UV-visible spectra of MeSO 2 and PhSO 2 radicals, indicating that the most important transition observed in this region is due to transfer of electrons from the lone pair orbitals of the oxygen atoms to... [Pg.1093]

The potential applications of NIR OFCD determination of metal ions are numerous. The detection of metal contaminants can be accomplished in real-time by using a portable fiber optical metal sensor (OFMD). Metal probe applications developed in the laboratory can be directly transferred to portable environmental applications with minimal effort. The response time of the NIR probe is comparable to its visible counterparts and is much faster than the traditional methods of metal analysis such as atomic absorption spectroscopy, polarography, and ion chromatography. With the use of OFMD results can be monitored on-site resulting in a significant reduction in labor cost and analysis time. [Pg.209]

The luminescence of diamonds is related to various defects in its structure. Almost always, luminescence centers in diamonds are related to N atoms. It is logical, because the atomic radii of C and N are nearly equal (approximately 0.77 A). Luminescence spectroscopy has proven to be the most widely used method in studies of diamonds even in comparison with optical absorption, ESR, IR and Raman spectroscopies. Himdreds of spectra have been obtained, fluorescence characteristics enter into diamond quality gemological certificates, a wide range of electronic and laser applications are based on diamond optical properties in excited states nitrogen center aggregation is controlled by the residence time of diamond in the mantle, distinction between natural... [Pg.116]

Analysis. Ca gives a brick-red flame coloration, indicating that various optical spectroscopies will be effective in its determination. Ca is quantitatively determined by colorimetry down to 100 ppb using murexide or o-cresolphthalein, by atomic absorption spectroscopy (AAS) to 20 ppb, to 1 ppb by electrothermal absorption spectroscopy (ETAS), to 0.01 ppb by inductively-coupled plasma emission spectroscopy (ICPES), and to 10 ppb by inductively-coupled plasma mass spectroscopy (ICPMS). A spot test for Ca which extends to 3 ppm is provided by glyoxal bis(2-hydroxyanil). [Pg.139]

Optical Transitions of the Halogen Atoms observed by Absorption Spectroscopy in the Vacuum Ultraviolet... [Pg.8]


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