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NNR IN RAPIDLY ROTATED METALS By - Nottingham eTheses ...

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CHAPTER 8<br />

MEASUREMENTS ON VANADIUM, NIOBIUM AND CADMIUM <strong>METALS</strong><br />

8.1 <strong>IN</strong>TRODUCTION<br />

In practice the number of metals which can usefully be investi-<br />

gated using the magic angle rotation technique is limited. Although<br />

the more common metals all possess at least one isotope with a<br />

nuclear magnetic moment, the natural abundance of many of these is<br />

extremely low. This fact combined with low values of magnetic<br />

moment- means that the resonances of a number of isotopes are extrem-<br />

ely weak. Such isotopes are unsuited to the macroscopic rotat-<br />

ion technique using existing equipment: indeed for many isotopes<br />

the resonance condition lay outside the range of the spectrometer.<br />

For those nuclear isotopes with spin greater than } existing in non-<br />

cubic lattices, quadrupole interactions lead to very broad character-<br />

istic spectra. Of those metals with cubic or near cubic lattice<br />

symmetry scandium, ß-manganese, tantalum and thallium still have<br />

too large a -static<br />

linewidth to be narrowed completely by the rotat-<br />

ion rates which can be achieved at present. In the other extreme,<br />

at room temperature the secular line broadening interactions in the<br />

alkali metals are already reduced by diffusional motion. The room<br />

temperature linewidths of lead and platinum arise in large part from<br />

T1 broadening, which is unaffected by macroscopic specimen rotation.<br />

Consequently these two metals were also excluded from the list of<br />

possible samples.

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