Spectral distribution of scattered light by fluid mixtures of correlated atoms and molecules

1981 ◽  
Vol 59 (11) ◽  
pp. 1620-1626 ◽  
Author(s):  
S. Kielich ◽  
T. Bancewicz ◽  
S. Woźniak

A stochastic theory of the spectral distribution of light scattered by mixtures of atoms and molecules, colliding in time and space, is proposed. New time-correlation functions C(0)(t) and C(2)(t) are introduced describing respectively the statistical microscopic mechanisms of isotropic and anisotropic coherent scattering, related with changes in the first and second perturbation of the molecular polarizability tensor due to the long-range fields of induced molecular electric multipoles. In this way, not only anisotropic but also isotropic scattering is shown to have a rotational spectral structure due to orientational motions and angular collisions of the polar molecules. The hitherto not considered cross approximations 0,1 and 0,2 of the functions C(0)(t) and C(2)(t) involve the first power of the dipole–quadrupole, dipole–octupole, and quadrupole–quadrupole tensors thus permitting first determinations of the signs of the successive multipolar molecular polarizabilities.

2017 ◽  
Vol 813 ◽  
pp. 205-249 ◽  
Author(s):  
Rohit Dhariwal ◽  
Sarma L. Rani ◽  
Donald L. Koch

The relative velocities and positions of monodisperse high-inertia particle pairs in isotropic turbulence are studied using direct numerical simulations (DNS), as well as Langevin simulations (LS) based on a probability density function (PDF) kinetic model for pair relative motion. In a prior study (Rani et al., J. Fluid Mech., vol. 756, 2014, pp. 870–902), the authors developed a stochastic theory that involved deriving closures in the limit of high Stokes number for the diffusivity tensor in the PDF equation for monodisperse particle pairs. The diffusivity contained the time integral of the Eulerian two-time correlation of fluid relative velocities seen by pairs that are nearly stationary. The two-time correlation was analytically resolved through the approximation that the temporal change in the fluid relative velocities seen by a pair occurs principally due to the advection of smaller eddies past the pair by large-scale eddies. Accordingly, two diffusivity expressions were obtained based on whether the pair centre of mass remained fixed during flow time scales, or moved in response to integral-scale eddies. In the current study, a quantitative analysis of the (Rani et al. 2014) stochastic theory is performed through a comparison of the pair statistics obtained using LS with those from DNS. LS consist of evolving the Langevin equations for pair separation and relative velocity, which is statistically equivalent to solving the classical Fokker–Planck form of the pair PDF equation. Langevin simulations of particle-pair dispersion were performed using three closure forms of the diffusivity – i.e. the one containing the time integral of the Eulerian two-time correlation of the seen fluid relative velocities and the two analytical diffusivity expressions. In the first closure form, the two-time correlation was computed using DNS of forced isotropic turbulence laden with stationary particles. The two analytical closure forms have the advantage that they can be evaluated using a model for the turbulence energy spectrum that closely matched the DNS spectrum. The three diffusivities are analysed to quantify the effects of the approximations made in deriving them. Pair relative-motion statistics obtained from the three sets of Langevin simulations are compared with the results from the DNS of (moving) particle-laden forced isotropic turbulence for $St_{\unicode[STIX]{x1D702}}=10,20,40,80$ and $Re_{\unicode[STIX]{x1D706}}=76,131$. Here, $St_{\unicode[STIX]{x1D702}}$ is the particle Stokes number based on the Kolmogorov time scale and $Re_{\unicode[STIX]{x1D706}}$ is the Taylor micro-scale Reynolds number. Statistics such as the radial distribution function (RDF), the variance and kurtosis of particle-pair relative velocities and the particle collision kernel were computed using both Langevin and DNS runs, and compared. The RDFs from the stochastic runs were in good agreement with those from the DNS. Also computed were the PDFs $\unicode[STIX]{x1D6FA}(U|r)$ and $\unicode[STIX]{x1D6FA}(U_{r}|r)$ of relative velocity $U$ and of the radial component of relative velocity $U_{r}$ respectively, both PDFs conditioned on separation $r$. The first closure form, involving the Eulerian two-time correlation of fluid relative velocities, showed the best agreement with the DNS results for the PDFs.


2003 ◽  
Vol 3 (1) ◽  
pp. 145-160 ◽  
Author(s):  
R. Lang ◽  
J. E. Williams ◽  
W. J. van der Zande ◽  
A. N. Maurellis

Abstract. We use a recently proposed spectral sampling technique for measurements of atmospheric transmissions called the Spectral Structure Parameterization (SSP) in order to retrieve total water vapor columns (WVC) from reflectivity spectra measured by the Global Ozone Monitoring Experiment (GOME). SSP provides a good compromise between efficiency and speed when performing retrievals on highly structured spectra of narrow-band absorbers like water vapor. We show that SSP can be implemented in a radiative transfer scheme which treats both direct-path absorption and absorption by singly-scattered light directly. For the retrieval we exploit a ro-vibrational overtone band of water vapor located in the visible around 590 nm. We compare our results to independent values given by the data assimilation model of ECMWF. In addition, results are compared to those obtained from the more accurate, but more computationally expensive, Optical Absorption Coefficient Spectroscopy (OACS).


Author(s):  
Wieland Schöllkopf

AbstractWhen Otto Stern embarked on molecular-beam experiments in his new lab at Hamburg University a century ago, one of his interests was to demonstrate the wave-nature of atoms and molecules that had been predicted shortly before by Louis de Broglie. As the effects of diffraction and interference provide conclusive evidence for wave-type behavior, Otto Stern and his coworkers conceived two matter-wave diffraction experiments employing their innovative molecular-beam method. The first concept assumed the molecular ray to coherently scatter off a plane ruled grating at grazing incidence conditions, while the second one was based on the coherent scattering from a cleaved crystal surface. The latter concept allowed Stern and his associates to demonstrate the wave behavior of atoms and molecules and to validate de Broglie’s formula. The former experiment, however, fell short of providing evidence for diffraction of matter waves. It was not until 2007 that the grating diffraction experiment was retried with a modern molecular-beam apparatus. Fully resolved matter-wave diffraction patterns were observed, confirming the viability of Otto Stern’s experimental concept. The correct explanation of the experiment accounts for quantum reflection, another wave effect incompatible with the particle picture, which was not foreseen by Stern and his contemporaries.


1976 ◽  
Vol 47 (2) ◽  
pp. 729-735 ◽  
Author(s):  
Kunitsugu Soda ◽  
Izumi Nishio ◽  
Akiyoshi Wada

Symmetry ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 1971
Author(s):  
Elena V. Orlenko ◽  
Fedor E. Orlenko

A non-Anderson weak localization of an electron beam scattered from disordered matter is considered with respect to the principle of electron indistinguishability. A weak localization of electrons of a new type is essentially associated with inelastic processing. The origin of inelasticity is not essential. We take into account the identity principle for electron beam and electrons of the atom of the scatterer with an open shell. In spite of isotropic scattering by each individual scatterer, the electron exchange contribution has a hidden parameters effect on the resulting angular dependence of the scattering cross-section. In this case, the electrons of the open shell of an atomic scatterer can be in the s-state, that is, the atomic shell remains spherically symmetric. The methods of an invariant time-dependent exchange perturbation theory and a Green functions with exchange were applied. An additional angular dependence of the scattering cross-section appears during the coherent scattering process. It is shown exactly for the helium scatterer that the role of exchange effects in the case of a singlet is negligible, while for the triplet state, it is decisive, especially for those values of the energy of incident electrons when de Broglie’s waves are commensurate with the atomic.


2011 ◽  
Author(s):  
Wilson Marques ◽  
Gilberto M. Kremer ◽  
Miriam Pandolfi Bianchi ◽  
Ana Jacinta Soares

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