Verbesserung des Meß-und Auswerteverfahrens zur Bestimmung der gemeinsamen und partiellen Diffusionskoeffizienten am Beispiel von Kupfer-Gold-Legierungen/An Improved Method for Measuring and Analysing Chemical and Intrinsic Diffusion Coefficients Applied to Copper-Gold Alloys

1975 ◽  
Vol 30 (10) ◽  
pp. 1282-1289 ◽  
Author(s):  
Th. Heumann ◽  
Th. Rottwinkel

Abstract A method is described which enables the determination of the chemical diffusion coefficients D̃ in a binary system as well as the intrinsic diffusion coefficients of both components with sufficient accuracy. The difference in concentration between the diffusion couples should not exceed 5 at%. Numerous diffusion profiles at different annealing times are taken by electron microprobe analysis from each specimen before calculating D̃ according to a method proposed by Sauer and Freise Combining the results for different pairs of specimens with overlapping concentration range mean values of D̃ are obtained in the total concentration range unter consideration. An analytical expression for D̃ is given, which is used to determine the diffusion profile for a special diffusion couple according to the method of Wagner4 . By this one obtains the total diffusion profile including the flat ends which cannot be accurately determinated by electron microprobe analysis. The determination of the intrinsic diffusion coefficients according to van Loo5 is based on these calculated profiles with additional knowledge of the position of the welding interface. This method has been applied to diffusion measurements in Cu-Au alloys. The following relation for D̃ has been found in the concentration range between 0 and 32 at% Au at 911 °C D̃(N)Cu Au911 °C =3,71·10-10 + 5.04·10-9 N+1.76·10-10 N2 + 1.01 -10-11 N3 [cm2 sec-1 ]. N = mole fraction of Au.

1990 ◽  
Vol 102 (4-6) ◽  
pp. 201-212
Author(s):  
Alex von Bohlen ◽  
Stefan Brüggerhoff ◽  
Reinhold Klockenkämper

1976 ◽  
Vol 24 (6) ◽  
pp. 749-751 ◽  
Author(s):  
V S Sottiurai ◽  
R L Malvin ◽  
L F Allard ◽  
W C Bigelow

A method is described for the determination of the intracellular concentration of sodium in individual cells using the electron microprobe analyzer. This method gives an accuracy equal to that obtained by using flame photometry on tissues with large cell populations. Intracellular sodium was precipitated in the cell by a fixative containing pyroantimonate. Cartilaginous needles from shark fins which were equilibrated in saline solutions of differing concentrations were used as biological standards.


1987 ◽  
Vol 59 (7) ◽  
pp. 930-937 ◽  
Author(s):  
Bert J. Raeymaekers ◽  
Xiande. Liu ◽  
Koen H. Janssens ◽  
Piet J. Van Espen ◽  
Fred C. Adams

1999 ◽  
Vol 84 (1-2) ◽  
pp. 78-85 ◽  
Author(s):  
Vladimir N. Sobolev ◽  
Catherine A. McCammon ◽  
Lawrence A. Taylor ◽  
Gregory A. Snyder ◽  
Nikolai V. Sobolev

Author(s):  
R. I. Johnsson-Hegyeli ◽  
A. F. Hegyeli ◽  
D. K. Landstrom ◽  
W. C. Lane

Last year we reported on the use of reflected light interference microscopy (RLIM) for the direct color photography of the surfaces of living normal and malignant cell cultures without the use of replicas, fixatives, or stains. The surface topography of living cells was found to follow underlying cellular structures such as nuceloli, nuclear membranes, and cytoplasmic organelles, making possible the study of their three-dimensional relationships in time. The technique makes possible the direct examination of cells grown on opaque as well as transparent surfaces. The successful in situ electron microprobe analysis of the elemental composition and distribution within single tissue culture cells was also reported.This paper deals with the parallel and combined use of scanning electron microscopy (SEM) and the two previous techniques in a study of living and fixed cancer cells. All three studies can be carried out consecutively on the same experimental specimens without disturbing the cells or their structural relationships to each other and the surface on which they are grown. KB carcinoma cells were grown on glass coverslips in closed Leighto tubes as previously described. The cultures were photographed alive by means of RLIM, then fixed with a fixative modified from Sabatini, et al (1963).


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