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1.
Phys Rev Lett ; 115(2): 025503, 2015 Jul 10.
Artigo em Inglês | MEDLINE | ID: mdl-26207479

RESUMO

We report on an extensive characterization of the cracking noise produced by charcoal samples when dampened with ethanol. We argue that the evaporation of ethanol causes transient and irregularly distributed internal stresses that promote the fragmentation of the samples and mimic some situations found in mining processes. The results show that, in general, the most fundamental seismic laws ruling earthquakes (the Gutenberg-Richter law, the unified scaling law for the recurrence times, Omori's law, the productivity law, and Båth's law) hold under the conditions of the experiment. Some discrepancies were also identified (a smaller exponent in the Gutenberg-Richter law, a stationary behavior in the aftershock rates for long times, and a double power-law relationship in the productivity law) and are related to the different loading conditions. Our results thus corroborate and elucidate the parallel between the seismic laws and fracture experiments caused by a more complex loading condition that also occurs in natural and induced seismicity (such as long-term fluid injection and gas-rock outbursts in mining processes).

2.
Phys Rev E Stat Nonlin Soft Matter Phys ; 86(5 Pt 1): 051705, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23214803

RESUMO

We demonstrate theoretically that the presence of ions in insulating materials such as nematic liquid crystals may be responsible for the dielectric spectroscopy behavior observed experimentally. It is shown that, at low frequencies, an essentially non-Debye relaxation process takes place due to surface effects. This is accomplished by investigating the effects of the adsorption-desorption process on the electrical response of an electrolytic cell when the generation and recombination of ions is present. The adsorption-desorption is governed by a non-usual kinetic equation in order to incorporate memory effects related to a non-Debye relaxation and the roughness of the surface. The analysis is carried out by searching for solutions to the drift-diffusion equation that satisfy the Poisson equation relating the effective electric field to the net charge density. We also discuss the effect of the mobility of the ions, i.e., situations with equal and different diffusion coefficients for positive and negative ions, on the impedance and obtain an exact expression for the admittance. The model is compared with experimental results measured for the impedance of a nematic liquid crystal sample and a very good agreement is obtained.


Assuntos
Íons/química , Cristais Líquidos/química , Modelos Químicos , Modelos Moleculares , Adsorção , Simulação por Computador , Impedância Elétrica , Propriedades de Superfície
3.
J Chem Phys ; 135(11): 114704, 2011 Sep 21.
Artigo em Inglês | MEDLINE | ID: mdl-21950880

RESUMO

The electrical response of an electrolytic cell in which the diffusion of mobile ions in the bulk is governed by a fractional diffusion equation of distributed order is analyzed. The boundary conditions at the electrodes limiting the sample are described by an integro-differential equation governing the kinetic at the interface. The analysis is carried out by supposing that the positive and negative ions have the same mobility and that the electric potential profile across the sample satisfies the Poisson's equation. The results cover a rich variety of scenarios, including the ones connected to anomalous diffusion.

4.
Eur Phys J E Soft Matter ; 24(3): 247-50, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18034217

RESUMO

The phase diagram is an interesting field of research, particularly in lyotropic liquid crystals (LLC). In this way, one of the most important phase diagrams of this LLC system was reported by Yu and Saupe. Two uniaxial (calamitic--N(C) and discotic--N(D)) and one biaxial nematic (N(B)) phases were determined by these authors. Furthermore, in this phase diagram the classical isotropic phase (I was observed at high temperature as well as a reentrant isotropic phase (I(RE)) which takes place at lower temperature. Later, this phase diagram was also studied by several authors and in all cases the I(RE)-N(C)-I phase transitions were not observed. In this work, we present a study of this phase diagram through digital image processing and refractometry optical techniques. The occurrence of these phase transitions is investigated and characterized. In addition, the order parameter is obtained based on the Vuks hypothesis from a particular point, in the range of the N(C) phase, where the absolute value of the optical birefringence (Deltan is maximum.

5.
Phys Rev E Stat Nonlin Soft Matter Phys ; 74(6 Pt 1): 062701, 2006 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-17280107

RESUMO

In this work, through the Z-scan technique, we report on measurements of the nonlinear refractive index (n{2}) in discotic and calamitic nematic phases at room temperature in lyotropic mixtures of potassium laurate, decanol and D(2)O . This technique presents high sensitivity when compared to conventional interferometry. The nonlinear optical birefringence (Deltan{2}) of these nematic phases was also determined. The sign and absolute value of this relevant nonlinear parameter are discussed in terms of structural changes in the micellar configuration which takes place in each nematic lyotropic phase.

6.
Phys Rev E Stat Nonlin Soft Matter Phys ; 65(5 Pt 2): 057602, 2002 May.
Artigo em Inglês | MEDLINE | ID: mdl-12059766

RESUMO

In this work the temperature dependence of the extraordinary/ordinary refractive indices and optical birefringence are determined near the reentrant isotropic (I(RE))-calamitic nematic (N(C)) and N(C)-isotropic (I) phase transitions in a lyotropic mixture of potassium laurate, decanol, and water. This reentrant isotropic phase is verified by our experimental data and discussed in terms of thermal variation of the micellar shape anisotropy. The results showed also, with basis in the Vuks's equation, that near the maximum optical birefringence in the range of N(C) phase the extraordinary coefficient of electronic polarizability (phi(parallel)) is equal to the ordinary coefficient (phi( perpendicular)).

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