Long‐time magnetic relaxation measurements on a quench melt growth YBCO superconductor

1994 ◽  
Vol 76 (10) ◽  
pp. 6950-6952 ◽  
Author(s):  
L. H. Bennett ◽  
L. J. Swartzendruber ◽  
M. J. Turchinskaya ◽  
J. E. Blendell ◽  
J. M. Habib ◽  
...  
1998 ◽  
Vol 11 (11) ◽  
pp. 1241-1250 ◽  
Author(s):  
M Holiastou ◽  
M Pissas ◽  
D Niarchos ◽  
P Haibach ◽  
U Frey ◽  
...  

2014 ◽  
Vol 30 ◽  
pp. e118-e119
Author(s):  
G. Kalaitzakis ◽  
L. Kavroulakis ◽  
T. Boursianis ◽  
S. Veneti ◽  
L. Kontopodis ◽  
...  

2021 ◽  
Vol 38 (7) ◽  
pp. 077201
Author(s):  
Yang Wang ◽  
Cong Li ◽  
Yong Li ◽  
Xuebo Zhou ◽  
Wei Wu ◽  
...  

Author(s):  
Kiyoshi Sawano ◽  
Mitsuru Morita ◽  
Masamoto Tanaka ◽  
Keiichi Kimura ◽  
Seiki Takebayashi ◽  
...  

1970 ◽  
Vol 25 (11) ◽  
pp. 1674-1680
Author(s):  
Hans Lütje

Abstract The nuclear magnetic relaxation times T1 and T2 may be determined by observing the relaxation that follows after a stop of an adiabatic fast passage at different points of the resonance signal. High resolution measurements are possible with external proton stabilization during the relaxation process if the chemical shifts are larger than 1 ppm and the relaxation times are longer than 1 sec. If no high resolution is required the lower limit is 0.2 seconds. Relaxation measurements are possible using conventional NMR-spectrometers without additional equipment. Since the signal to noise ratio is favourable, rather dilute solutions may be investigated. Relaxation measurements on benzene, on 4 different protons of 4-dimethylamino-benzaldehyde and on polyethylene oxide in solution are reported.


2004 ◽  
Vol 18 (10) ◽  
pp. 548-552 ◽  
Author(s):  
E. Romanus ◽  
N. Matoussevitch ◽  
S. Prass ◽  
J. Heinrich ◽  
R. Müller ◽  
...  

2000 ◽  
Vol 334 (1-2) ◽  
pp. 115-122 ◽  
Author(s):  
E.V Blinov ◽  
H Huhtinen ◽  
E Lähderanta ◽  
Yu Stepanov ◽  
K Traito ◽  
...  

1979 ◽  
Vol 177 (1) ◽  
pp. 303-309 ◽  
Author(s):  
N Boden ◽  
M C Holmes ◽  
P F Knowles

Proton nuclear-relaxation rates have been measured as a function of frequency, temperature, pH and cyanide concentration in aqueous solutions of superoxide dismutase from bovine erythrocytes. The results show that, whereas for pH less than or equal to 9 only one water molecule is bound to each Cu2+ ion, at higher pH a second co-ordination site for OH- becomes available; it is proposed that this involves cleavage of the bond between Cu2+ and the histidine residue that bridges to Zn2+.


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