Application of proton magnetic resonance soundings to groundwater reserve mapping in weathered basement rocks (Brittany, France)

2004 ◽  
Vol 175 (1) ◽  
pp. 21-34 ◽  
Author(s):  
Robert Wyns ◽  
Jean-Michel Baltassat ◽  
Patrick Lachassagne ◽  
Anatoly Legchenko ◽  
Jacques Vairon ◽  
...  

Abstract The Proton Magnetic Resonance (PMR) or Nuclear Magnetic Resonance (NMR) method, coupled with geometrical aquifer modelling, has been used to create a map of groundwater reserves over a 270 km2 study area in a weathered basement setting. Most of the reserves are contained in a stratiform multi-layer aquifer whose geometry is influenced by the weathering front. The depths to the interfaces determined by PMR are considered and validated by comparison with the geometrical approach. Water contents and decay times of the PMR signal for each weathered layer are compared with the hydrogeological model. The results of the study show a decrease in water content from the top downwards for the three main aquifer layers (respectively : unconsolidated alterite, and an upper and a lower fissured zone). The groundwater reserves (80 % in the fissured zone and 20 % in unconsolidated alterite) represent approximately three years of average infiltration.




Intelligence ◽  
2009 ◽  
Vol 37 (2) ◽  
pp. 192-198 ◽  
Author(s):  
Rex E. Jung ◽  
Charles Gasparovic ◽  
Robert S. Chavez ◽  
Arvind Caprihan ◽  
Ranee Barrow ◽  
...  


1973 ◽  
Vol 56 (1) ◽  
pp. 124-127 ◽  
Author(s):  
Eric B Sheinin ◽  
Walter R Benson ◽  
Myron M Smith

Abstract Disulfiram was determined in disulfiram drug substance and tablets by proton magnetic resonance (PMR) spectroscopy at the 100–480 mg level and by a colorimetric technique involving cuprous iodide at the 50 mg level. The tablet excipients do not interfere in the analysis. The average result for disulfiram in a tablet composite was 100.8±1.4% of label claim by PMR and 100.7±0.4% by the colorimetric method.



1967 ◽  
Vol 20 (8) ◽  
pp. 1663 ◽  
Author(s):  
JFK Wilshire

2-Fluoro-5-nitrobenzonitrile, an analogue of 1-fluoro-2,4- dinitrobenzene, in which the 2-nitro group has been replaced by a cyano group, has been prepared and made to react with several amines, amino acids, and NH-heteroaromatic compounds. The proton magnetic resonance spectra of some of the resultant N-(2-cyano-4-nitrophenyl) derivatives were compared with the spectra of the corresponding N-(2,4- dinitrophenyl) derivatives and furnish further evidence that the ortho nitro group of the latter derivatives is rotated out of the plane of the aromatic nucleus.





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