On the determination of the diffusion coefficient of heterogeneous aerosols by the dynamic method

1957 ◽  
Vol 37 (1) ◽  
pp. 183-190 ◽  
Author(s):  
L. W. Pollak ◽  
A. L. Metnieks
2003 ◽  
Vol 57 (1) ◽  
pp. 9-14
Author(s):  
Jelena Bastic ◽  
Dejan Skala ◽  
Slavica Ivanovic

The determination of specific characteristics of materials commonly used in the preparation of cloths for the protection of the human body, lungs and other human organs, based on the principles of the effective adsorption of highly toxic organic vapors initially requires the development of specific and reliable techniques for the preparation of a gas stream with the relevant highly toxic organic substances. The dynamic method, one of the techniques commonly used for material characterization, is based on the procedure of determining the concentration of different substances in the gas stream at the inlet and after passing through a specific thin layer of the adsorption material (outlet). Therefore, the generation of a gas phase containing highly toxic organic substances in a defined quantity during a specific time interval, is the requirement that must previously be fulfilled before using the dynamic method for testing specific materials for protection of the human body. Usually, a dynamic method of determining the quality of cloths prepared with specific adsorbents requires a relatively low volumetric flow rate of the gas phase containing the test substance which may be achieved by using a diffusion tube (DT) as the standard equipment for the generation of test substances. A very wide range of concentrations of the test substances in a specific gas phase (inert, air) can be obtained by varying the working conditions (temperature, pressure, gas flow rate) and the geometrical size of the diffusion tube, taking into account that the concentration of toxic substances, is determined as the ratio of their diffusion rate and from the DT and the carrier gas flow rate. The diffusion rate of the test substances from the DT is caused by the concentration gradient between the partial pressure of the saturated vapor at one end of the DT capillary and the partial pressure at the outlet of the diffusion tube according to Fick's law. The mass rate of the generated test substances from the DT is constant for constant conditions (temperature and pressure) in the reservoir of the DT On the basis of a detailed theoretical calculation such a rate (R) may be defined by the equation: R = 16.624 DM(P/T)(A/L)log [P/(P- pv)l, mg/min where: D - the diffusion coefficient, cm/s; M - the molar mass of the test substance, g/mol; P - the pressure in the DT kPa; pv - the vapor pressure of the test substance, kPa; A - the cross sectional area of the capillary of the DT cm2: L - the length of the capillary of the DT cm; T - the temperature, K. A procedure for the constant isothermal vapor generation of hydrogen cyanide (HCN) and 2-bromo-2-chloro-1,1,1-trifluoroethane (halotane) into air by a using diffusion tube is described. The DT was placed into a thermostat 0.5?C) and the diffusion rates of the substance were measured during some time interval and the above equation was used for the determination of the diffusion coefficient. The obtained data were correlated with the calculated ones on the basis of an empirical correlation from the literature. The relative differences in the experimentally determined and theoretically calculated values of the diffusion coefficient for hydrogen cyanide at different temperature (19-23.2?C) were 26-31 % and for halotane (26-45?C) 8-14%.


1984 ◽  
Vol 49 (10) ◽  
pp. 2349-2354 ◽  
Author(s):  
František Vláčil ◽  
Karel Koňák

The selectivity coefficients of the nitrate and chloride ions and of anionic chloro complexes of Au(III), Rh(III), Pd(II), and Pt(IV) for ion exchange on Spheron DEAE in the chloride form are determined by the dynamic method. the complex anion species formed are identified and the ion exchange nature of the sorption of precious metals on this sorbent is confirmed based on the elution order of the precious metals as determined previously by the column chromatography on Spheron DEAE using hydrochloric acid as the mobile phase. The effect of the presence of perchlorate in the mobile phase during the liquid chromatography of precious metals and during the chromatographic determination of nitrate traces is explained.


1996 ◽  
Vol 61 (6) ◽  
pp. 844-855 ◽  
Author(s):  
Olga Šolcová ◽  
Petr Schneider

It was shown that the sampling loop, detector and connecting elements in the chromatographic set-up for determination of transport parameters by the dynamic method significantly influence the response peaks from columns packed with porous or nonporous particles. A method, based on the use of convolution theorem, was developed which can take these effects into account. The applicability of this method was demonstrated on the case of axial dispersion in a single-pellet-string column (SPSR) packed with nonporous particles. It is possible to handle also responses from columns packed with porous particles by a similar procedure.


1996 ◽  
Vol 05 (01) ◽  
pp. 3-11 ◽  
Author(s):  
GÜLHAYAT NASÜN-SAYGILI ◽  
HASANCAN OKUTAN

1997 ◽  
Vol 496 ◽  
Author(s):  
M. Inaba ◽  
S. Nohmi ◽  
A. Funabiki ◽  
T. Abe ◽  
Z. Ogumi

ABSTRACTThe electrochemical permeation method was applied to the determination of the diffusion coefficient of Li+ion (DLi+) in a glassy carbon (GC) plate. The cell was composed of two compartments, which were separated by the GC plate. Li+ions were inserted electrochemically from one face, and extracted from the other. The flux of the permeated Li+ions was monitored as an oxidation current at the latter face. The diffusion coefficient was determined by fitting the transient current curve with a theoretical one derived from Fick's law. When the potential was stepped between two potentials in the range of 0 to 0.5 V, transient curves were well fitted with the theoretical one, which gaveDLi+ values on the order of 10−8cm2s−1. In contrast, when the potential was stepped between two potentials across 0.5 V, significant deviation was observed. The deviation indicated the presence of trap sites as well as diffusion sites for Li+ions, the former of which is the origin of the irreversible capacity of GC.


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