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401.
We have demonstrated more than 3 W of average output power from a 2.94-mu;m quasi-cw diode-pumped total internal reflection (TIR) Er:YAG laser operating at 100 Hz with a 4% duty cycle. Moreover, repetition rates of up to 600 Hz at more than 1.2-W output power have been achieved. The cavity consists of a plane-mirror resonator of 40-mm length and uses three of five TIR regions within the laser crystal as pump facets to efficiently couple the pump energy into the resonant laser mode. Differential efficiencies of up to 18.3% have been achieved at an optimum pump pulse width in the range of 300 micros .  相似文献   
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Using67Zn Mössbauer absorption and emission spectroscopy, we have investigated the electronic structure at the A and B sites in the normal spinels (Zn)[Al2]O4, (Zn)[Fe2]O4 and (Zn)[Ga2]O4. Within each system, the center shift Sc at the A site is more positive. In all systems investigated, the electric field gradientV u at the B site is negative. The values for SC andV U scale with oxygen nearest-neighbour distance to Zn. In the Fe spinel, a transferred magnetic hyperfine field is observed at the Zn site below the antiferromagnetic ordering temperatureT N=10 K. For a more detailed discussion of the chemical bond, we have performed ab initio Hartree-Fock cluster calculations for the Al and Fe spinels. Our experimental and theoretical results show that all hyperfine parameters are essentially determined by covalency effects. Our data on the Ga spinel raise the question of a partially inverse structure.  相似文献   
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We report on first experiments to investigate the electronic structure in the normal spinels ZnAl2O4 and ZnFe2O4 and in the inverse spinels Zn2SnO4 and Zn2TiO4 using the high-resolution67Zn-Mössbauer spectroscopy. The electric field gradient for67Zn at the B (octahedral) site in ZnAl2O4 is negative, whereas the A (tetrahedral) site remains essentially cubic, however, with a more positive center shift. ZnFe2O4 orders antiferromagnetically at ≈10K. Due to superexchange a magnetic field is observed at67Zn. In the inverse spinels short range order leads to only few (Zn,Sn) and (Zn,Ti) configurations at the octahedral sites. The s-electron densities at the67Zn sites are distinct and cover a surprisingly broad range for Zn2TiO4. This strongly suggests that d-electrons of Ti play an essential role in the chemical bond of this compound.  相似文献   
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The electron-capture decay of228Pa to levels in228Th has been studied using mass-separated sources and high-resolutionγ-ray and conversion-electron spectroscopy. A level at 979.5 keV is assigned as 2+ member of a second excited Kπ=0+ band, with the 0+ band head at 938.6 keV. The 2+ and 3+ members of a second excited Kπ=2+ band at 1153.5 and 1200.5 keV, which decay by strongE0 transitions to the 969 keVγ-vibrational band, are confirmed. In addition we tentatively propose a Kπ=1+ band at 944 keV. The Kπ=0?, 1? and 2? members of the octupole quadruplet are confirmed, and theγ decay of these levels is analysed in an approach, in which the mixing of the octupole bands by the Coriolis interaction is taken into account. It is suggested that octupole correlations might be important for theE1 transition moments. A total of 29 levels is observed between ~1.4 and ~2.0 MeV, for which the nuclear structure, and the possible assignment to rotational bands, is unclear.  相似文献   
408.
Excited states of the doubly-odd nucleus V6Br have been studied with in-beam γ-ray spectroscopy techniques. In addition to the positive parity band that has been extended up to I=(13) a Iπ=4? isomer (T1/2=0.5±0.2 ns) and two bands of negative parity have been identified. The bands are discussed in terms of two-quasiparticle configurations. For the band built on the 4? isomer the configuration πg9/2?νf5/2 or p3/2 is proposed.  相似文献   
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Zusammenfassung Es werden eine hochdruckflüssigkeits- und eine gas-chromatographische Methode zur quantitativen Bestimmung der Styrol-Metaboliten MandelsÄure und PhenylglyoxylsÄure im Urin beschrieben. Bei beiden Verfahren wird die PhenylglyoxylsÄure wegen der InstabilitÄt ihrer Derivate durch Oxidation mit Wasserstoffperoxid in der Urinprobe quantitativ zur BenzoesÄure decarboxyliert. Nach einer Flüssig-Flüssig-Extraktion werden die SÄuren mit Diazomethan verestert und dann chromatographiert. Die Probenaufarbeitung erfolgt unter den Bedingungen der internen Standardisierung. Zur Trennung der SÄureester wird bei der GLC ein Temperaturprogramm, bei der HPLC die Gradientenelution mit einer Reversed-Phase-SÄule eingesetzt. Die Detektion wird mit einem Flammenionisationsdetektor bzw. mit einem UV-Detektor mit variabler WellenlÄnge vorgenommen. Mit beiden Methoden wurden Urinproben von 24 styrolbelasteten Personen auf ihren MandelsÄure- und PhenylglyoxylsÄure-Gehalt untersucht. Es ergaben sich Korrelationskoeffizienten von r=0,980 bzw. r=0,916 für Mandelbzw. PhenylglyoxylsÄure.
Quantitative determination of the styrene metabolites mandelic acid and phenylglyoxylic acid in urine by high-performance liquid chromatography and gas chromatography
Summary In both the procedures described the urinary phenylglyoxylic acid is quantitatively decarboxylated to benzoic acid by means of an oxidation with hydrogen peroxide. After a liquid-liquid extraction and a subsequent methylation of the acids with diazomethane the chromatographic analysis is carried out. Internal standardization is used for both the methods. The gas chromatographic method uses a temperature program for the separation of the acid esters and a double-flame ionization detector for detection. High-performance liquid chromatography applies gradient elution on a reversed-phase column; a UV-detector with variable wave-length is used for detection. Checking of the reliability of both the methods was done by means of a parallel determination of mandelic and phenylglyoxylic acids in urine samples of 24 persons exposed to styrene. This resulted in a correlation coefficient of r=0.980 and r=0.916 for mandelic and phenylglyoxylic acid, respectively.
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