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21.
Absolute spectrophotometric measurements of the Swan bands of two comets have been compared with computed synthetic spectra using modern Franck-Condon and Hönl-London factors, and varying rotational, vibrational, and electronic excitation temperatures. Rotational and vibrational temperatures were obtained for the comets. Although the electronic excitation temperature and the molecular column density cannot be separated, a relationship is found between these two quantities. A review is made of recent determinations of column densities for CN in comets.  相似文献   
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The structure and dynamics of 2-dimensional fluids in swelling clays   总被引:3,自引:0,他引:3  
The interlayer pores of swelling 2:1 clays provide an ideal 2-dimensional environment in which to study confined fluids. In this paper we discuss our understanding of the structure and dynamics of interlayer fluid species in expanded clays, based primarily on the outcome of recent molecular modelling and neutron scattering studies. Counterion solvation is compared with that measured in bulk solutions, and at a local level the cation-oxygen coordination is found to be remarkably similar in these two environments. However, for the monovalent ions the contribution to the first coordination shell from the clay surfaces increases with counterion radius. This gives rise to inner-sphere (surface) complexes in the case of potassium and caesium. In this context, the location of the negative clay surface charge (i.e. arising from octahedral or tetrahedral substitution) is also found to be of major importance. Divalent cations, such as calcium, eagerly solvate to form outer-sphere complexes. These complexes are able to pin adjacent clay layers together, and thereby prevent colloidal swelling. Confined water molecules form hydrogen bonds to each other and to the clays' surfaces. In this way their local environment relaxes to close to the bulk water structure within two molecular layers of the clay surface. Finally, we discuss the way in which the simple organic molecules methane, methanol and ethylene glycol behave in the interlayer region of hydrated clays. Quasi-elastic neutron scattering of isotopically labelled interlayer CH3OD and (CH2OD)2 in deuterated clay allows us to measure the diffusion of the CH3- and CH2-groups in both clay and liquid environments. We find that in both the one-layer methanol solvates and the two-layer glycol solvates the diffusion of the most mobile organic molecules is close to that in the bulk solution.  相似文献   
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Rhenium and osmium isotopes in sulfide minerals from the Bagdad porphyry Cu–Mo deposit have been used to determine timing of mineralization and the source of osmium and, by inference, ore metals. Molybdenite, chalcopyrite and pyrite were analyzed mainly from the quartz monzonite and porphyritic quartz monzonite units, which are characterized by moderate to strong potassic alteration (secondary biotite and K-feldspar). Rhenium concentrations in molybdenite are between 330 and 642 ppm. Four Re–Os analyses of two molybdenite samples from the quartz monzonite and porphyritic quartz monzonite yield a weighted average age of 71.8±0.2 Ma (2s). Analyses of a third sample from a molybdenite vein in Precambrian rocks, outside of the main ore zone, yield a weighted average age of 75.9±0.2 Ma (2s), and provide evidence of two separate mineralization episodes. Chalcopyrite samples contain 6 to 12 ppt Os and 1.7 to 4.1 ppb Re; 187Os/ 188Os initial ratios are between 0.1 and 0.8. Pyrite samples have osmium and rhenium concentrations varying in the range 8–17 ppt and 3.9–6.8 ppb, respectively. Analyses from these pyrite samples yield an eight-point isochron with an age of 77±15 Ma (2s) and an initial 187Os/ 188Os ratio of 2.1±0.8 (MSWD=0.90). The results presented here add to the growing body of work indicating that porphyry-type mineralization is produced by long-term, multiple episodes of magmatism and associated mineralization. The data also support the hypothesis that a significant part of the metals and magmas may have a crustal source, as has been suggested for other copper deposits and districts in Arizona.  相似文献   
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We present an overview of our recent results on utilizing small earthquakes in the earthquake engineering practice. Site-specific ground motion time-histories of large earthquakes can be successfully simulated using recordings of small earthquakes which are often referred to as 'empirical Green's functions' in seismology. Another important practical problem is whether and how these observations can be used in seismic risk studies which are based on empirical attenuation relations for ground motion parameters. We study a possibility of extrapolating attenuation relations for small earthquakes, to larger magnitudes using the data from the Garner Valley downhole array in Southern California. Finally we introduce efficient ground motion processing techniques in frequency- and time-domains and apply them to site response estimation.  相似文献   
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When the output of a complex chemical model is analysed, a typical topic isthe determination of pathways, i.e., reaction sequences, that produce ordestroy a chemical species of interest.A representative example is the investigation of catalytic ozone destruction cycles in the stratosphere.An algorithm for the automatic determination of pathways in any given reactionsystem is presented. Under the assumption that reaction rates are known, it finds all significant pathways, i.e., all pathways with a rate above a prescribed threshold.The algorithm forms pathways step by step, starting from single reactions.The chemical species in the system are consecutively considered as `branching points'.For every branching-point species, each pathway producing it is connected witheach pathway consuming it.Rates proportional to `branching probabilities' are calculated.Pathways with a rate that is smaller than a prescribed threshold arediscarded.If a newly formed pathway contains sub-pathways, e.g., null cycles, it is split into these simpler pathways.In order to demonstrate the performance of the algorithm, it has been applied to the determination of catalytic ozone destruction cycles and methaneoxidation pathways in the stratosphere.  相似文献   
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