Page 23 - Fiber Fracture
P. 23

8                                                             K.K. Chawla

                fibers as well  as to the presence of  microvoids and  the  skin-core  structure of  these
                fibers. It  should be  pointed  out  that  poor  properties  in  shear  and  compression are,
                however, also observed in other highly oriented polymeric fibers such as polyethylene
                and poly@-phenylene benzobisoxazole) or PBO fibers, which are not based on rigid-rod
                polymers. A  correlation between good  compressive characteristics and  a  high  glass
                transition temperature (or melting point) has been suggested (Northolt, 198 1; Kozey and
                Kumar, 1994).
                  Thus,  with  the  glass  transition  temperature  of  organic  fibers  being  lower  than
                that of  inorganic fibers, the  former would  be  expected to  show poorer properties in
                compression. For aramid and similar fibers, compression results in the formation of kink
                bands leading to eventual ductile failure. Yielding is observed at about 0.5% strain. This
                is thought to correspond to a  molecular rotation of  the amide carbon-nitrogen  bond
                from the normal extended trans configuration to a kinked configuration Tanner et al.,
                1986). This causes a 45" bend in the chain, which propagates across the unit cell, the
                microfibrils, and a kink band results in the fiber.
                  Efforts to  improve  the  compressive properties  of  rigid-rod  polymer  fibers  have
                involved introduction of cross-linking in the transverse direction. There is a significant
                effect  of  intermolecular  interaction  or  intermolecular  cross-linking  on  compressive
                strength. A polymeric fiber (PPD) with a compressive strength of  1.6 GPa has been
                reported  (Jenkins  et  al.,  2001).  This  high  compressive  strength  is  ascribed  to  bi-
                directional, intermolecular hydrogen bonding. A high degree of intermolecular covalent
                cross-linking should result in higher compressive strength, as compared to systems in
                which only hydrogen bonding is present (Jenkins et al., 2001). However, cross-linking
                may also result in lower tensile strength and increased brittleness of  the fiber. Cross-
                linking by thermal treatment may result in the development of  internal stresses. Other
                cross-linking methods (e.g.  via  radiation) should be  explored in  greater detail.  One
                would expect radiation to result in a different cross-linked structure than that obtained
                by thermal treatment. Here it is instructive to compare the behavior of  some carbon
                fibers.  Highly  graphitic,  mesophase pitch-based fibers  show  a  fibrillar fracture  and
                poor compressive properties. PAN-based carbon fibers, which have some linking of thc
                graphitic planes in the transverse direction, show better properties in compression and
                not a very fibrillar fracture. Of course metallic and ceramic fibers show little fibrillation
                during a tensile or compressive failure.


                Environmental Effects on Polymeric Fibers
                  Environmental  factors  such  as  humidity,  temperature,  pH,  ultraviolet  radiation,
                and  micro-organisms can  affect  the  strength  and  the  fracture  process  in  polymeric
                fibers. Natural polymeric fibers are more susceptible to environmental degradation than
                synthetic polymeric fibers. Cellulose is attacked by  a  variety of  bacteria, fungi, and
                algae. Micro-organisms use cellulose as a food source. Natural fibers based on protein
                such as wool, hair, silk, etc., can also be a food source for micro-organisms, but  such
                fibers are more prone to degradation due to humidity and temperature. Polymeric fibers,
                natural  or  synthetic, undergo photo  degradation when  exposed to light (both visible
                and ultraviolet). Physically this results in discoloration, but is also accompanied by  a
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