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Carbon nanotube-reinforced polymer nanocomposite fibers   81


                 6000
                                                17.2                        50
                     1s
                 4000                 PAN
                                      PAN/GO
                E′ (MPa)              PAN/C 60  2q (degree)  17.1           40
                                      PAN/CNT
                 2000                           17.0
                                                                   2q (110,200)
                                                16.9               Xc (%)
                                                                   XS (A)
               (A)  0 0    60      120     180  (B)  0  2  4   6   8  10  12  30
                             Time (min)                   Time duration (h)
                    Amorphous                                            Amorphous
                    polymer            Amorphous    Crystalline  Graphitic  carbon
                              Crystalline  polymer  polymer  structure
                              polymer
                                   1s
                                                        Carbonization


               (C)
              Fig. 5.6  (A) Storage modulus versus dynamic strain durations for PAN film and C 60 /PAN,
              GO/PAN, MWNT/PAN composite films; (B) plots of the structural parameters of MWNT/
              PAN films versus dynamic strain durations [42]; and (C) schematic of PAN interphase
              development during dynamic straining and the resulting carbonized structures [29].
              (Source of (A) and (B): Y. Li, P. Zhou, F. An, Y. Liu, C. Lu, Dynamic self-stiffening and struc-
              tural evolutions of polyacrylonitrile/carbon nanotube nanocomposites, ACS Appl. Mater.
              Interfaces 9 (6) (2017) 5653–5659. Source of (C): Y. Li, Y. Yu, Y. Liu, C. Lu, Interphase develop-
              ment in polyacrylonitrile/SWNT nano composite and its effect on cyclization and carboniza-
              tion for tuning carbon structures, ACS Appl. Nano Mater. 1 (7) (2018) 3105–3113.)

              of PAN chains. The structural change of the nanocomposites was also depen-
              dent on the direction of the dynamic straining, that is, the growth direction
              of PAN crystals was perpendicular to the straining direction, while there was
              no structural change observed along the straining direction. A scheme of the
              interphase growth during dynamic straining is shown in Fig. 5.6C. For PAN/
              CNT nanocomposites, the interphase PAN would form graphitized struc-
              tures during carbonization at a temperature between 1100°C and 1300°C.

              5.2.3  Properties of CNT-containing fibers
              Besides the improvement of mechanical properties, the incorporation of
              CNTs in a polymer fiber can also affect other properties of the fiber, such as
              glass transition temperature and thermal shrinkage, electrical conductivity,
              thermal conductivity, and solvent resistance.
                 CNT restricts  the polymer chain mobility in its vicinity. For PAN/
              SWNT nanocomposite fibers, the glass transition temperature increased
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