Molecular Water Motions of Skim Milk Powder Solutions during Acidification Studied by17O and1H Nuclear Magnetic Resonance and Rheology

2011 ◽  
Vol 59 (18) ◽  
pp. 10097-10103 ◽  
Author(s):  
Sandie M. Møller ◽  
Andrew K. Whittaker ◽  
Jason R. Stokes ◽  
Michael J. Gidley ◽  
Ulf Andersen ◽  
...  
1977 ◽  
Vol 44 (1) ◽  
pp. 125-130 ◽  
Author(s):  
R. E. Hester ◽  
D. E. C. Quine

SummaryA small process analyser employing the pulsed nuclear magnetic resonance technique has been used to determine both water and fat contents of milk powder and cottage cheese samples. The procedures used for establishing and eliminating cross-interferences in these analyses are described. For milk powders, water and fat contents in the ranges 1–5 and 0·5–25 % respectively were determined with standard deviations of 0·20 % water and 0·64 % fat. Cottage cheese samples with water and fat contents in the ranges 77–81 and 2–7 % respectively were determined with standard deviations of 0·30 % water and 0·16 % fat.


2021 ◽  
Vol 11 (6) ◽  
pp. 14127-14141

This paper presents the characteristics of potato and apple tissues, with/out electroporation, by Time Domain-Nuclear Magnetic Resonance (TD-NMR). A portable TD-NMR was used to measure the proton relaxation time, T2, and the changes in the cells due to molecular water mobility of potato tubers,-NMR to identify the modifications that occurred at the cell level involving water molecules mobility in potato tubers and apple tissues after the electroporation treatment and compared with non-electroporated ones. The comparisons with normal potato and apple tissue and preliminary measurements in bulk were performed. Samples were also analyzed in terms of conductivity of the tissue and microscopic morphology. The results indicate that the electroporation process effect is identified with a variation of the peak position in T2 distribution, associated with sub-cell modifications.


Author(s):  
M.J. Hennessy ◽  
E. Kwok

Much progress in nuclear magnetic resonance microscope has been made in the last few years as a result of improved instrumentation and techniques being made available through basic research in magnetic resonance imaging (MRI) technologies for medicine. Nuclear magnetic resonance (NMR) was first observed in the hydrogen nucleus in water by Bloch, Purcell and Pound over 40 years ago. Today, in medicine, virtually all commercial MRI scans are made of water bound in tissue. This is also true for NMR microscopy, which has focussed mainly on biological applications. The reason water is the favored molecule for NMR is because water is,the most abundant molecule in biology. It is also the most NMR sensitive having the largest nuclear magnetic moment and having reasonable room temperature relaxation times (from 10 ms to 3 sec). The contrast seen in magnetic resonance images is due mostly to distribution of water relaxation times in sample which are extremely sensitive to the local environment.


Author(s):  
Paul C. Lauterbur

Nuclear magnetic resonance imaging can reach microscopic resolution, as was noted many years ago, but the first serious attempt to explore the limits of the possibilities was made by Hedges. Resolution is ultimately limited under most circumstances by the signal-to-noise ratio, which is greater for small radio receiver coils, high magnetic fields and long observation times. The strongest signals in biological applications are obtained from water protons; for the usual magnetic fields used in NMR experiments (2-14 tesla), receiver coils of one to several millimeters in diameter, and observation times of a number of minutes, the volume resolution will be limited to a few hundred or thousand cubic micrometers. The proportions of voxels may be freely chosen within wide limits by varying the details of the imaging procedure. For isotropic resolution, therefore, objects of the order of (10μm) may be distinguished.Because the spatial coordinates are encoded by magnetic field gradients, the NMR resonance frequency differences, which determine the potential spatial resolution, may be made very large. As noted above, however, the corresponding volumes may become too small to give useful signal-to-noise ratios. In the presence of magnetic field gradients there will also be a loss of signal strength and resolution because molecular diffusion causes the coherence of the NMR signal to decay more rapidly than it otherwise would. This phenomenon is especially important in microscopic imaging.


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