Nuclear Magnetic Resonance in Exchange-Enhanced Metals:Rh103Knight Shifts and Relaxation Rates in Palladium-Rhodium and Nickel-Rhodium Alloys

1971 ◽  
Vol 3 (3) ◽  
pp. 616-625 ◽  
Author(s):  
Albert Narath ◽  
H. T. Weaver
2004 ◽  
Vol 851 ◽  
Author(s):  
Sarah C. Chinn ◽  
Julie L. Herberg ◽  
April M. Sawvel ◽  
Robert S. Maxwell

ABSTRACTSiloxanes have a wide variety of applications throughout the aerospace industry which take advantage of their exceptional insulating and adhesive properties and general resilience. They also offer a wide range of tailorable engineering properties with changes in composition and filler content. They are, however, subject to degradation in radiatively and thermally harsh environments. We are using solid state nuclear magnetic resonance techniques to investigate changes in network and interfacial structure in siloxane elastomers and their correlations to changes in engineering performance in a series of degraded materials. Nuclear magnetic resonance (NMR) parameters such as transverse (T2) relaxation times, cross relaxation rates, and residual dipolar coupling constants provide excellent probes of changes crosslink density and motional dynamics of the polymers caused by multi-mechanism degradation. The results of NMR studies on aged siloxanes are being used in conjunction with other mechanical tests to provide insight into component failure and degradation kinetics necessary for preliminary lifetime assessments of these materials as well as into the structure-property relationships of the polymers. NMR and magnetic resonance imaging (MRI) results obtained both from high resolution NMR spectrometers as well as low resolution benchtop NMR screening tools will be presented.


1992 ◽  
Vol 119 (2) ◽  
pp. 157-164 ◽  
Author(s):  
G. J. McDougall ◽  
B. A. Goodman ◽  
J. A. Chudek

SUMMARYNuclear magnetic resonance (NMR) micro-imaging techniques have been employed to study noninvasively the spatial distribution of mobile protons (1H) around the cotyledonary node of flax (Linum usitatissimum) plants of two differing growth morphologies. The gross anatomy of the tissues of the stem can be discerned as a result of differences in their mobile 1H contents. The technique produced excellent images of the complex changes in stem structure that occur at the point of origin of side shoots. Detailed structure within the xylem could be visualized and the presence of fibre bundles deduced as dark areas amongst tissues of higher 1H signal intensity.As a result of the non-invasive and non-destructive nature of NMR-imaging, the images obtained have been compared to micrographs obtained by conventional histological techniques on the same plant tissue. In general, the two approaches produce comparable results, but the NMR images are influenced by the relaxation properties of the protons as well as their concentration. Paramagnetic species, such as Mn2+ ions, produce enhanced relaxation rates of protons in their vicinity and an apparent increase in proton density at short recycle times. Thus an NMR image can yield both chemical and structural information. Some of the advantages and disadvantages of this technique over conventional histological methods are discussed.


1974 ◽  
Vol 52 (6) ◽  
pp. 924-929 ◽  
Author(s):  
George Kotowycz

The influence of paramagnetic Cu2+ ions on the proton decoupled 13C n.m.r. spectra of pyrimidine nucleosides and nucleotides has been studied. For 5′-CMP, the C5 resonance is broadened first on the addition of Cu2+ ions followed by the C2, C4, and C1′ resonances. From a comparison of the transverse and longitudinal relaxation rates of the base carbon nuclei due to the presence of Cu2+ ions, binding of Cu2+ to the N3 nitrogen of 5′-CMP is predicted. A similar broadening behavior is observed for 5′-UMP, 5′-TMP, cytidine, and uridine. This indicates that the Cu2+ ion is located near the N3 nitrogen in these Cu2+-nucleoside and -nucleotide complexes.


2016 ◽  
Vol 3 (3) ◽  
pp. 150705 ◽  
Author(s):  
Richard J. Foster ◽  
Robin A. Damion ◽  
Thomas G. Baboolal ◽  
Stephen W. Smye ◽  
Michael E. Ries

Aggrecan, a highly charged macromolecule found in articular cartilage, was investigated in aqueous salt solutions with proton nuclear magnetic resonance. The longitudinal and transverse relaxation rates were determined at two different field strengths, 9.4 T and 0.5 T, for a range of temperatures and aggrecan concentrations. The diffusion coefficients of the water molecules were also measured as a function of temperature and aggrecan concentration, using a pulsed field gradient technique at 9.4 T. Assuming an Arrhenius relationship, the activation energies for the various relaxation processes and the translational motion of the water molecules were determined from temperature dependencies as a function of aggrecan concentration in the range 0–5.3% w/w. The longitudinal relaxation rate and inverse diffusion coefficient were approximately equally dependent on concentration and only increased by upto 20% from that of the salt solution. The transverse relaxation rate at high field demonstrated greatest concentration dependence, changing by an order of magnitude across the concentration range examined. We attribute this primarily to chemical exchange. Activation energies appeared to be approximately independent of aggrecan concentration, except for that of the low-field transverse relaxation rate, which decreased with concentration.


1987 ◽  
Vol 41 (7) ◽  
pp. 1194-1199 ◽  
Author(s):  
David L. Ashley ◽  
Elizabeth R. Barnhart ◽  
Donald G. Patterson ◽  
Robert H. Hill

Nuclear magnetic resonance (NMR) techniques are used to determine the chlorination pattern on a number of chlorinated pyrenes and pyrene-addition products. Determining chemical shifts, couplings, and longitudinal relaxation rates makes the unequivocal assignment of these molecules possible. Chlorination under the conditions described here were found to follow the normal orientation rules for pyrene. Spectral parameters obtained from these molecules are consistent enough to allow further application to unknown compounds. This should simplify assigning NMR spectra to other chlorinated pyrene standards.


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