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Close to a supercritical Hopf bifurcation, oscillatory media may be described, by the complex Ginzburg-Landau equation. The most important spatiotemporal behaviors associated with this dynamics are reviewed here. It is shown, on a few concrete examples, how real chemical oscillators may be described by this equation, and how its coefficients may be obtained from the experimental data. Furthermore, the effect of natural forcings, induced by the experimental realization of chemical oscillators in batch reactors, may also be studied in the framework of complex Ginzburg-Landau equations and its associated phase dynamics. We show, in particular, how such forcings may locally transform oscillatory media into excitable ones and trigger the formation of complex spatiotemporal patterns.  相似文献   
33.
We have calculated the leading and next-to-leading logarithm coefficients ofO(α s 2 )e + e ? annihilation jet cross sections, thrust distribution and energy-energy correlation in the two-jet limit when the jet resolution and the event shape variables vanish. We have compared our results with expectations based on leading logarithm approximations used to resum the pertubative cross sections where this is possible. There is good agreement for the leading and next-to-leading coefficients of jet cross sections in the Durham scheme. Also for the thrust distribution and energy-energy correlation we find results which are consistent with the leading logarithm predictions.  相似文献   
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A flame photometric method of determining calcium in phosphate, carbonate, and silicate locks has been developed Aluminum and phosphate interference was overcome by the addition of a large excess of magnesium. The method is rapid and suitable for routine analysis Results obtained are within ± 2% of the calcium oxide content.  相似文献   
36.
We calculate the cross section fore + e 3 jets for longitudinally polarized virtual photons up to order s 2 in the quark-gluon coupling.Dedicated to the memory of Kurt Symanzik  相似文献   
37.
The electroanalytical determination of avidin in solution, in a carbon paste, and in a transgenic maize extract was performed in acidic medium at a carbon paste electrode (CPE). The oxidative voltammetric signal resulting from the presence of tyrosine and tryptophan in avidin was observed using square-wave voltammetry. The process could be used to determine avidin concentrations up to 3 fM (100 amol in 3 l drop) in solution, 700 fM (174 fmol in 250 l solution) in an avidin-modified electrode, and 174 nM in a maize seed extract. In the case of the avidin-modified CPE, several parameters were studied in order to optimize the measurements, such as electrode accumulation time, composition of the avidin-modified CPE, and the elution time of avidin. In addition, the avidin-modified electrode was used to detect biotin in solution (the detection limit was 7.6 pmol in a 6 l drop) and to detect biotin in a pharmaceutical drug after various solvent extraction procedures. Comparable studies for the detection of biotin were developed using HPLC with diode array detection (HPLC-DAD) and flow injection analysis with electrochemical detection, which allowed biotin to be detected at levels as low as 614 pM and 6.6 nM, respectively. The effects of applied potential, acetonitrile content, and flow rate of the mobile phase on the FIA-ED signal were also studied.  相似文献   
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INAA was used to obtain genetic informations on basalts through their weathering and sedimentary products. The rare earths content of the samples could be determined with sufficient accuracy without radiochemical separation using routine computer programs. Basalts of different tectonic setting could be distinguished by their rare earths, thorium and uranium contents. Relations between magmatic rock fragments and sedimentary environment (including manganese nodules) of the Romanche Zone (Atlantic) are discussed.  相似文献   
40.
The ultrafast N-O bond fragmentation in a series of N-methoxypyridyl radicals, formed by one-electron reduction of the corresponding N-methoxypyridiniums, has been investigated as potentially barrierless electron-transfer-initiated chemical reactions. A model for the reaction involving the electronic and geometric factors that control the shape of the potential energy surface for the reaction is described. On the basis of this model, molecular structural features appropriate for ultrafast reactivity are proposed. Femtosecond kinetic measurements on these reactions are consistent with a kinetic definition of an essentially barrierless reaction, i.e., that the lifetime of the radical is a few vibrational periods of the fragmenting bond, for the p-methoxy-N-methoxypyridyl radical.  相似文献   
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