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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

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