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1.
Summary We are going to present the focal-mechanism solution of Fruili earthquake occurred on May 6, 1976, as it results from the
analysis, on original seismograms, of the polarities of initial longitudinal waves obtained in 92 seismic stations. The polarities
so obtained have been reported on the projection which represents the surface of the Earth and the solution has been drawn,
directly, from the study of the resulting distribution, by establishing through Gr?fe's theory the two couples of forces considered
as the sources of the seism at the focus. At last, a comparison has been carried out with the solution already obtained by
other authors.
Riassunto Si presenta la soluzione del meccanismo focale del terremoto del Fruili del 6/5/1976 ottenuta dallo studio, sui sismogrammi originali, della polarità delle onde longitudinali iniziali, quale si è presentata in 92 stazioni sismiche vicine e lontane. Le polarità ottenute sono state riportate sulla superficie della Terra e la soluzione è stata ricavata direttamente dallo studio della distribuzione così ottenuta, definendo mediante la teoria di Gr?fe le due coppie di forze che hanno agito all'ipocentro. Un confronto è stato infine eseguito con le soluzioni in precedenza ottenute da altri autori.
Резюме Предлагается решение фокального механизма землетрясения, имевшего место в Фриули 6 мая 1976 г. Решение есть результат анализа исходных сейсмограмм, которые получены на 92 сейсмнческих, удаленнынных и близких. Полученные пояьрности представлены в проекции на поверхность Земли. Решение получено непосредственно из исследования результируюшего распределения, которое следует из теории Грефа для для двух пар сил, представляюших источники землетрясения в фокусе. В заключение проводится сравнение с решением, полученным ранее другими авторами.相似文献
2.
Experimental Techniques - 相似文献
3.
Oscar E. Piro Eduardo E. Castellano Roberto C. V. Piatti Agustín E. Bolzn Alejandro J. Arvia 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(4):m252-m255
The crystal structures of two salts of bis(thiourea)gold(I) complexes, namely bis(thiourea‐κS)gold(I) chloride, [Au(CH4N2S)2]Cl, (I), and bis[bis(thiourea‐κS)gold(I)] sulfate, [Au(CH4N2S)2]2SO4, (II), have been determined. The chloride salt, (I), is isomorphous with the corresponding bromide salt, although there are differences in the bonding. The AuI ion is located on an inversion centre and coordinated by two symmetry‐related thiourea ligands through the lone pairs on their S atoms [Au—S 2.278 (2) Å and Au—S—C 105.3 (2)°]. The sulfate salt, (II), crystallizes with four independent [Au(CH4N2S)2]+ cations per asymmetric unit, all with nearly linear S—Au—S bonding. The cations in (II) have similar conformations to that found for (I). The Au—S distances range from 2.276 (3) to 2.287 (3) Å and the Au—S—C angles from 173.5 (1) to 177.7 (1)°. These data are relevant in interpreting different electrochemical processes where gold–thiourea species are formed. 相似文献
4.
de Namor AF Chahine S Castellano EE Piro OE Jenkins HD 《Chemical communications (Cambridge, England)》2005,(30):3844-3846
An additive thermodynamic contribution of pendant arms to the complexation of calixarene derivatives with mercury(II) in acetonitrile is for the first time demonstrated. 相似文献
5.
6.
Pablo Albores Zulema D. Chaia Luis Baraldo Eduardo E. Castellano Oscar E. Piro 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(4):m235-m236
The octahedral title compound, [Ru(C2H5O)(NO)(NO2)2(C6H16N2)], crystallizes in the rhombohedral space group P31 with an ethoxy ligand axially coordinated trans to the nitrosyl ligand. The RuII ion is equatorially coordinated by a tetramethylethylenediamine group acting as a bidentate ligand, and to two nitro moieties whose planes are tilted with respect to the mean equatorial plane. Each nitrogen ligand bonded to the metallic centre has a different hybridization state. 相似文献
7.
Danil de Namor AF Chahine S Castellano EE Piro OE 《The journal of physical chemistry. A》2005,109(30):6743-6751
The solvent control on the ability of a partially substituted lower rim calix(4)arene derivative 5,11,17,23,tetra-tert-butyl[25,27-bis(hydroxy)-26,28-bis(ethylthioethoxy)]-calix(4)arene, 1 to host soft metal cations (Hg(II) and Ag(I)) is demonstrated through 1H NMR, electrochemical (conductance measurements), and thermodynamic characterization of the complexation process in a wide variety of solvents. Solvent-ligand interactions were assessed from 1H NMR measurements involving 1 and various solvents in CDCl3. Thus, the formation of a 1:1 1-CH3CN adduct is reported. As far as metal cations are concerned, depending on the medium their complexation with 1 was only observed for Hg(II) and Ag(I). Thus, in acetonitrile, 1 is more selective for Hg(II) relative to Ag(I) by a factor of 2.2 x 10(3). In methanol the selectivity is reversed to an extent that the affinity of 1 for Ag(I) is 1.4 x 10(3) higher than that for Hg(II). However, 1 is unable to recognize selectively these cations in N,N-dimethylformamide while in propylene carbonate the ability of 1 to interact with these cations is lost. An outstanding feature of thermodynamics emerges when an assessment is made of the ligand effect on the complexation of these cations and analogues calix(4)arene derivatives. Thus, in acetonitrile the thermodynamics of cation complexation by the hydrophilic cavity of a calix(4)arene containing mixed pendant groups is built up from thermodynamic data for the same process involving derivatives with common functionalities at the narrow rim. This is a unique example of the additive contribution of pendant arms in the field of thermodynamics of calixarene chemistry. 相似文献
8.
Maria Ana Castro Zulema D. Chaia Oscar E. Piro Fabio D. Cukiernik Eduardo E. Castellano Marcia Rusjan 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(7):m393-m395
The title compound, tetrakis(μ‐3,4,5‐triethoxybenzoato‐κ2O:O′)bis[(pyrazine‐κN)rhodium(II)](Rh—Rh), [Rh2(C13H17O5)4(C4H4N2)2], crystallizes on an inversion centre in the triclinic space group . The equatorial carboxylate ligands bridge the two RhII atoms, giving a binuclear lantern‐like structure. The pyrazine molecules occupy the two axial coordination sites. The phenyl rings are tilted by ca 10° with respect to the attached carboxylate groups. The pyrazine planes have a torsion angle of ca 19° around the Rh—N bond with respect to the plane of the nearer carboxylate group and are not coplanar with the Rh—Rh bond. 相似文献
9.
Andrs Zelcer Zulema D. Chaia Fabio D. Cukiernik Oscar E. Piro Eduardo E. Castellano 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(3):m144-m146
The title compound, catena‐poly[[tetrakis(μ‐decanoato‐κ2O:O′)diruthenium(II,III)(Ru—Ru)]‐μ‐octanesulfonato‐κ2O:O′], [Ru2(C10H19O2)4(C8H17O3S)], is an octanesulfonate derivative of the mixed‐valence complex diruthenium tetradecanoate. The equatorial carboxylate ligands are bidentate, bridging two Ru atoms to form a dinuclear structure. Each of the two independent dinuclear metal complexes in the asymmetric unit is located at an inversion centre. The octanesulfonate anion bridges the two dinuclear units through axial coordination. The alkyl chains of the carboxylate and sulfonate ligands are arranged in a parallel manner. The global structure can be seen as infinite chains of polar moieties separated by a double layer of non‐polar alkyl groups, without interdigitation of the alkyl chains. 相似文献
10.
The dynamics of small spherical neutrally buoyant particulate impurities immersed in a two-dimensional fluid flow are known to lead to particle accumulation in the regions of the flow in which vorticity dominates over strain, provided that the Stokes number of the particles is sufficiently small. If the flow is viewed as a Hamiltonian dynamical system, it can be seen that the accumulations occur in the nonchaotic parts of the phase space: the Kolmogorov-Arnold-Moser tori. This has suggested a generalization of these dynamics to Hamiltonian maps, dubbed a bailout embedding. In this paper we use a bailout embedding of the standard map to mimic the dynamics of neutrally buoyant impurities subject not only to drag but also to fluctuating forces modeled as white noise. We find that the generation of inhomogeneities associated with the separation of particle from fluid trajectories is enhanced by the presence of noise, so that they appear in much broader ranges of the Stokes number than those allowing spontaneous separation. (c) 2002 American Institute of Physics. 相似文献