NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...
NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...
NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...
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3.1 <strong>IN</strong>TRODUCTION<br />
- 31 -<br />
CHAPTER 3<br />
NARROW<strong>IN</strong>G THE NUCLEAR RESONANCE SPECTRUM BY<br />
MACROSCOPIC SAMPLE ROTATION<br />
In Chapter 2 the various line-broadening interactions which<br />
exist in solids, and metals in particular, have been considered.<br />
In many liquids and solids the situation is different: motion of<br />
the nuclear spins averages out the secular line broadening mechan-<br />
ism. ' The internal motion may be described by a correlation funct-<br />
ion f(v) with a mean correlation time Tc. If Tc is short and less<br />
than T2 (the characteristic time describing the dephasing of spins<br />
in the rotating frame) the spin vectors will execute a random walk<br />
in the rotating frame and only slowly accumulate a phase difference<br />
relative to the mean resonance frequency vo. In the extreme case<br />
the secular interactions become so inefficient that the width of<br />
the resonance spectrum is determined by the homogeneity of the<br />
magnetic field across the sample and lifetime broadening.<br />
The above discussion is concerned with microscopic motion with-<br />
in a particular sample. Similar arguments apply when studying<br />
the effect of a macroscopic rotation of the sample about a unique<br />
axis, but there are a few important differences. Unlike random<br />
internal motion, macroscopic rotation only causes averaging over<br />
the plane of rotation and not over inter-nuclear distances. Macro-<br />
scopic motion is a very slow process by molecular standards and<br />
involves a single frequency of motion. Although Fourier analysis