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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- 70 -<br />
sequence may be repeated. In practice the PGI was used to measure<br />
the signal amplitude at a fixed time after the second pulse. Once<br />
a constant value was recorded the pulse separation T was changed<br />
and the procedure repeated.<br />
5.8.2 DIPOLAR RELAXATION TIME (TID)<br />
Measurements of T1D (or more accurately Tis) were under-<br />
taken using the 90-T-4590-t'-4590 pulse sequence of Jeener and<br />
(69)<br />
Brockaert. In this sequence two rf pulses 900 out of phase<br />
are used to transfer Zeeman order into observable amounts of dipolar<br />
order. We include below a simple explanation as to the effect<br />
of this pulse sequence on the nuclear spin system.<br />
The first 900 pulse aligns the spins along the y* axis in the<br />
rotating frame. After a time t ti T2 the spins have dephased so<br />
that the fast spins point along the +x* axis direction and the<br />
slow spins along the -x* direction. The second pulse along y*<br />
turns the fast spins along the -z direction and the slow spins<br />
along the +z direction. Once the remaining transverse magnet-<br />
ization has decayed to zero this corresponds to a state of dipolar<br />
order, i. e. an absorption spectrum which is absorptive above vo<br />
and emissive below. Although this explanation is based on two<br />
90° pulses the transfer of order is most efficient when the second<br />
pulse length is reduced to 450. A third pulse, again 45 0, is<br />
used to detect the amount of dipolar order after a time t'.<br />
Experimentally the sequence was set up in the same manner as<br />
described by Tunstall and Brown (72) and will not be reiterated<br />
here. The delay unit described in Section 5.2 was used to step