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gence provides overall molecular orientation. Limited studies have
reported on the use of off-line polarized Raman spectroscopy to esti-
mate orientation in fi lms [12,14,66] and fi bers [13,67,68] . The detailed
procedure for determining the orientation of the polymer specimens
by polarized Raman spectroscopy was presented by Bower [69] . Later
studies [12,13,67] proposed approaches to simplify the experimental
complexities.
Paradkar et al. [23] demonstrated the use of Raman spectroscopy
for measuring molecular orientation during fi ber spinning of i- PP. They
used the ratio of Raman peaks at 841 and 809 cm − 1 , which is sensitive
to the molecular anisotropy in PP, to estimate a semiquantitative
molecular orientation in the fi ber line for different throughput and
draw ratios. Figure 3.13 shows the real-time ZZ polarized Raman
spectra for PP obtained at three different positions along the fi ber line.
The ratio of the 841- to 809-cm − 1 peak was reported to decrease as the
Near die
3
2.5
Near feed roll
2
1.5
1
Between feed and
draw rolls
0.5
0
600
800
1000
1200
1400
Raman shift (cm -1 )
Figure 3.13 Polarized Raman spectra (ZZ) representing development of molecular
orientation in polypropylene at three different locations in the fi ber-spinning line.
(Reproduced from Paradkar et al. [23].)
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