Measurements of mobilities and longitudinal diffusion coefficients of Na+ ions in Ne, Ar, and CH4 at room temperature by a continuous guard‐ring system

1983 ◽  
Vol 79 (8) ◽  
pp. 3893-3899 ◽  
Author(s):  
K. Iinuma ◽  
M. Takebe ◽  
Y. Satoh ◽  
K. Seto
1980 ◽  
Vol 73 (4) ◽  
pp. 2012-2013 ◽  
Author(s):  
M. G. Thackston ◽  
M. S. Sanchez ◽  
G. W. Neeley ◽  
W. M. Pope ◽  
F. L. Eisele ◽  
...  

Clay Minerals ◽  
1998 ◽  
Vol 33 (2) ◽  
pp. 255-267 ◽  
Author(s):  
D. Tessier ◽  
M. Dardaine ◽  
A. Beaumont ◽  
A. M. Jaunet

AbstractClay from Fourges has been selected by the Commissariat à l'Energie Atomique as a support in radioactive waste disposal studies. This material was activated by adding Na2CO3, then compacted at 60 MPa. Subsequently, its swelling behaviour was monitored at 90°C and 145°C for 330 days and at the end of this period the samples were examined by transmission electron microscopy (TEM). For this, they were embedded in a resin then sectioned with an ultramicrotome for mineralogical and chemical analyses. The initial material is essentially composed of kaolinite and smectite. Addition of Na2CO3 at room temperature induces a replacement of Ca ions by Na ions and the precipitation of finely divided carbonates on the surface of the constituents. At the end of 330 days at 90°C under a hydraulic pressure of 1 MPa, the initial particles combine and the material exerts a swelling pressure of 20 MPa. A complete reorganisation of the clay crystallites is observed without significant dissolution of the solid phases. After the same time at 145°C under a hydraulic pressure of 10 MPa, in a basic medium, the combined conditions are such that a high proportion of the clay is dissolved with formation of amorphous aluminosilicates correlated with a marked drop in the swelling pressure to 5 MPa. This work establishes the advantages of following the macroscopic properties in parallel with the microstructure variations for understanding the changes in the properties of clays.


2006 ◽  
Vol 20 (5-6) ◽  
pp. 261-268 ◽  
Author(s):  
Cristina M. Muntean ◽  
Rolf Misselwitz ◽  
Heinz Welfle

The influence of Mn2+ions on the structure of natural calf thymus DNA was studied by Raman spectroscopy. Measurements were done at room temperature and pH 6.2±0.2, in the presence of the physiological concentration of 150 mM Na+ions, and in the presence of Mn2+concentrations that varied between 0 and 600 mM. No condensation of DNA was observed at any of the Mn2+concentrations. At 5 mM Mn2+and 150 mM Na+no significant influence of Mn2+ions on the DNA structure can be observed. Compared with our previous results obtained at 10 mM Na+ions, binding of Mn2+ions to charged phosphate groups and to DNA bases is inhibited in the presence of 150 mM Na+ions. DNA backbone conformational changes were not observed in the whole concentration range of Mn2+ions as judging from the Raman spectra. No evidence for DNA melting was identified. A high Mn2+affinity for binding to guanine N7 and possibly, in a much lesser extent, to adenine have been found.


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