Page 411 - Handbook of Properties of Textile and Technical Fibres
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384                             Handbook of Properties of Textile and Technical Fibres


                      0.3
                               DR 2.5 normal
                               DR 2.5 quenched
                               DR 3.5 normal
                      0.2
                    Estimated ν TT  (–)  0.1  DR 4.5 normal
                               DR 3.5 quenched
                               DR 4.5 quenched






                      0.0
                        0.0  1.0   2.0   3.0   4.0    5.0   6.0   7.0
                                    Fiber modulus (GPa)
         Figure 12.19 Relation between initial modulus and the portion of taut tie molecules for PA 6
         fibers (according to (Mishra and Deopura, 1982)).


            For calculation of the property P, it is therefore necessary to know P c ,P a ,v TT , and
         v c . In their work Mishra and Deopura (1982) used the initial modulus E as the
         property; for PA 6 they adopted the following values E c ¼ 24.0 GPa and
         E a ¼ 0.7 Gpa, and they measured X-rayebased crystallinity. Then they calculated
         from the known fiber initial modulus E the corresponding portion of taut tie molecules
         v TT .
            Results for PA 6 fibers drawn to three draw ratios (25, 3.5, and 4.5) and partially
         quenched by a quenching system with a temperature of about  16 C are shown in

         Fig. 12.19.
            It is interesting that the dependence between E and v TT is practically linear, which
         supports the hypothesis that the taut tie molecules play a major role in determining the
         properties of PA fibers.
            More recently, the portion of taut tie molecules v TT between 0.04 and 0.10 was
         estimated from nuclear magnetic resonance results (Zhizhenkov and Egorov, 1984).
         One reason for the differences can be probable errors in the equation for the calculation
         of v TT using the modulus E.
            Assessment of molecular orientation in polyamides is simply based on the bire-
         fringence measurement (Lim et al., 1989). Hermans et al. (1946) provided a thor-
         ough analysis of the orientation factor, f, and its effects on axial alignment of
         macromolecules. Ziabicki and Kedzierska (Lim et al., 1989; Ziabicki and
         Kedzierska, 1959, 1962) proved that the birefringence of the as-spun fibers
         increases at a monotonic rate with the reciprocal of fiber diameter. Also, Ishibashi
         (Lim et al., 1989; Ishibashi et al., 1970) provided an equation that describes how
         birefringence decreases with spinning temperature.
            A theoretical framework developed by Shigemitsu et al. (1998) can be used for
         analyzing intensity of polarized fluorescence in an anisotropic polymer and its direct
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