The Effect of Differences in the Diffusion Coefficients of Components on the Onset of Convection in Isothermal Multicomponent Systems

2016 ◽  
Vol 367 ◽  
pp. 96-102
Author(s):  
Vladimir Kossov ◽  
Yuriy Zhavrin ◽  
Olga Fedorenko

Two series of experiments on the formation of convective flows in multicomponent liquid and gaseous mixtures are considered. In the first series, the convective structures arising during the diffusion of a binary aqueous solution of salt and sugar in an aqueous solution of pure salt were studied using the schlieren method. The observed behavior of convective cells corresponds to the instability similar to the "finger structures". In the second series, the experiments were conducted to determine the effective diffusion coefficients as a function of pressure in gas mixtures 0.5504 CH4 + 0.4496 Ar – N2 and 0.5994 H2 + 0.4006 Ar – N2. Our experiments have shown that the onset of convective flows both in liquid and gaseous multicomponent mixtures is due to the difference in the interdiffusion coefficients of the components. The experimental data for the ternary gas mixtures are described in the framework of the linear theory of stability.

1927 ◽  
Vol 10 (4) ◽  
pp. 575-598 ◽  
Author(s):  
L. Michaelis ◽  
W. A. Perlzweig

The theoretical aspects of the problem of sieve-like membranes are developed. The method of preparing the dried collodion membrane is described, and the method of defining the property of a particular membrane is given. It consists of the measurement of the Co P, that is the P.D. between an 0.1 and an 0.01 M KCl solution separated by the membrane. Co P is in the best dried membranes 50 to 53 millvolts, the theoretically possible maximum value being 55 millivolts. Diffusion experiments have been carried out with several arrangements, one of which is, for example, the diffusion of 0.1 M KNO3 against 0.1 M NaCl across the membrane. The amount of K+ diffusing after a certain period was in membranes with a sufficiently high Co P (about 50 millivolts or more) on the average ten times as much as the amount of diffused Cl-. In membranes with a lower Co P the ratio was much smaller, down almost to the proportion of 1:1 which holds for the mobility of these two ions in a free aqueous solution. When higher concentrations were used, e.g. 0.5 M solution, the difference of the rate of diffusion for K+ and Cl- was much smaller even in the best membranes, corresponding to the fact that the P.D. of two KCl solutions whose concentrations are 10:1 is much smaller in higher ranges of concentration than in lower ones. These observations are confirmed by experiments arranged in other ways. It has been shown that, in general, the diffusion of an anion is much slower than the one of a cation across the dried collodion membrane. The ratio of the two diffusion coefficients would be expected to be calculable in connection with the potential difference of such a membrane when interposed between these solutions. The next problem is to show in how far this can be confirmed quantitatively.


1965 ◽  
Vol 43 (2) ◽  
pp. 431-435 ◽  
Author(s):  
Harry Watts

The diffusion coefficient of trace amounts of xenon-133 has been measured in binary mixtures of xenon with helium, neon, argon, and krypton. Measurements were made over the complete composition range in the pressure range 10–300 Torr at 302.6 °K. These systems are the first studied in which the results do not agree with the equation:[Formula: see text],which relates the effective diffusion coefficient of a trace in an ideal gas mixture to binary diffusion coefficients and the composition of the mixture. Deviation from this equation can not be accounted for in terms of the known deviation of xenon from ideal gas behavior.The self-diffusion coefficient of xenon was 0.060 and the binary diffusion coefficients Xe–He 0.535, Xe–Ne 0.230, Xe–Ar 0.127, Xe–Kr 0.0823, in cm2 s−1 corrected to 1 atm pressure.


2014 ◽  
Vol 758 ◽  
pp. 407-435 ◽  
Author(s):  
Céline Guervilly ◽  
David W. Hughes ◽  
Chris A. Jones

AbstractUsing numerical simulations of rapidly rotating Boussinesq convection in a Cartesian box, we study the formation of long-lived, large-scale, depth-invariant coherent structures. These structures, which consist of concentrated cyclones, grow to the horizontal scale of the box, with velocities significantly larger than the convective motions. We vary the rotation rate, the thermal driving and the aspect ratio in order to determine the domain of existence of these large-scale vortices (LSV). We find that two conditions are required for their formation. First, the Rayleigh number, a measure of the thermal driving, must be several times its value at the linear onset of convection; this corresponds to Reynolds numbers, based on the convective velocity and the box depth, $\def \xmlpi #1{}\def \mathsfbi #1{\boldsymbol {\mathsf {#1}}}\let \le =\leqslant \let \leq =\leqslant \let \ge =\geqslant \let \geq =\geqslant \def \Pr {\mathit {Pr}}\def \Fr {\mathit {Fr}}\def \Rey {\mathit {Re}}{\gtrsim }100$. Second, the rotational constraint on the convective structures must be strong. This requires that the local Rossby number, based on the convective velocity and the horizontal convective scale, ${\lesssim }0.15$. Simulations in which certain wavenumbers are artificially suppressed in spectral space suggest that the LSV are produced by the interactions of small-scale, depth-dependent convective motions. The presence of LSV significantly reduces the efficiency of the convective heat transport.


2007 ◽  
Vol 263 ◽  
pp. 189-194
Author(s):  
Ivo Stloukal ◽  
Jiří Čermák

Coefficient of 65Zn heterodiffusion in Mg17Al12 intermetallic and in eutectic alloy Mg - 33.4 wt. % Al was measured in the temperature region 598 – 698 K using serial sectioning and residual activity methods. Diffusion coefficient of 65Zn in the intermetallic can be written as DI = 1.7 × 10-2 m2 s-1 exp (-155.0 kJ mol-1 / RT). At temperatures T ≥ 648 K, where the mean diffusion path was greater than the mean interlamellar distance in the eutectic, the effective diffusion coefficient Def = 2.7 × 10-2 m2 s-1 exp (-155.1 kJ mol-1 / RT) was evaluated. At two lower temperatures, the diffusion coefficients 65Zn in interphase boundaries were estimated: Db (623 K) = 1.6 × 10-12 m2 s-1 and Db (598 K) = 4.4 × 10-13 m2 s-1.


2021 ◽  
Author(s):  
Christos Katsavrias ◽  
Ioannis A. Daglis ◽  
Afroditi Nasi ◽  
Constantinos Papadimitriou ◽  
Marina Georgiou

<p>Radial diffusion has been established as one of the most important mechanisms contributing the acceleration and loss of relativistic electrons in the outer radiation belt. Over the past few years efforts have been devoted to provide empirical relationships of radial diffusion coefficients (D<sub>LL</sub>) for radiation belt simulations yet several studies have suggested that the difference between the various models can be orders of magnitude different at high levels of geomagnetic activity as the observed D<sub>LL</sub> have been shown to be highly event-specific. In the frame of SafeSpace project we have used 12 years (2009 – 2020) of multi-point magnetic and electric field measurements from THEMIS A, D and E satellites to create a database of calculated D<sub>LL</sub>. In this work we present the first statistics on the evolution of D<sub>LL </sub>during the various phases of Solar cycle 24 with respect to the various solar wind parameters and geomagnetic indices.</p><p>This work has received funding from the European Union's Horizon 2020 research and innovation programme “SafeSpace” under grant agreement No 870437.</p>


2018 ◽  
Vol 107 (1) ◽  
pp. 39-54
Author(s):  
Chunli Wang ◽  
Xiaoyu Yang ◽  
Jiangang He ◽  
Fangxin Wei ◽  
Zhong Zheng ◽  
...  

Abstract To explore the diffusion behavior of 75Se(IV) in Beishan granite (BsG), the influences of temperature, oxygen condition and ionic strength were investigated using the through-diffusion experimental method. The effective diffusion coefficient De of 75Se(IV) in BsG varied from 4.21×10−14 m2/s to 3.19×10−13 m2/s in our experimental conditions, increased with increasing temperature. The formation factor Ff of BsG was calculated to be nearly constant in the range of temperatures investigated, suggesting that the inner structure of BsG had no significant change in the temperature range of 20–55°C. Meanwhile, the De values of 75Se(IV) in BsG under anaerobic condition was significantly larger than that under aerobic condition, which may be attributed to the difference in the sorption characteristics and species distribution of Se and pH values. Moreover, the diffusion of 75Se(IV) was promoted with ionic strength increased from 0.01 M to 0.1 M, and then decreased at 0.5 M, mainly due to the combined effects of reduced double layers with increased ionic strength and increase of the solution viscosity at higher ionic strength.


In a previous communication from these laboratories by G. A. Scott an account was given of the determination of the isotherms of hydrogen, carbon monoxide and mixtures of the two in the molecular proportion 2 : 1, 1 : 1 and 1 : 2 over a pressure range up to 170 atmospheres and at a temperature of 25° C. Since the completion of that investigation new apparatus has been installed so that the pressure and temperature ranges might be extended; and in this paper are embodied the results of further determinations carried out at both 0° C. and 25° C. and over a pressure range extending up to 600 atmospheres. In pursuing this investigation further it is our endeavour to furnish information in regard to the gaseous mixtures in question over the pressure and temperature ranges now commonly used in industrial processes. The Isotherms of the Single Gases . A repetition in our new apparatus of the determinations previously made by Scott both for the single gases and gas mixtures at 25° C. and at pressures up to 170 atmospheres showed his figures to be in close agreement with our own, the variations never exceeding 0·1 per cent.


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