Page 27 - Mechanics Analysis Composite Materials
P. 27

12                  Mechanics and anaIysis of composite materials
             filaments are made  in  approximately the  same manner  as for  glass fibers from
             molten petroleum or coal pitch and pass through carbonization and graphitization
             processes. Because pyrolysis is accompanied with a loss of material, carbon fibers
             have a porous structure and their specific gravity (about  1.8)  is less than that of
             graphite (2.26). The properties of carbon fibers are affected with the crystallite size,
             crystalline orientation, porosity and purity of carbon structure.
               Typical stress-strain  diagrams for high-modulus (HM)  and high-strength (HS)
             carbon fibers are plotted in  Fig.  1.7. As components of advanced composites for
             engineering applications, carbon fibers are characterized with very  high modulus
             and strength, high chemical and biological resistance, electricconductivity and very
             low Coefficient of thermal expansion. Strength of carbon fibers practically does not
             decrease under temperature elevated up to  1500°C (in the inert media preventing
             oxidation of fibers).
               The exceptional strength of 7.06 GPa is reached in Toray T-1000 carbon fibers,
             while  the  highest  modulus  of  850 GPa  is  obtained  in  Carbonic  HM-85  fibers.
             Carbon fibers are anisotropic, very  brittle, and sensitive to damage. They do not
             absorb water and change their dimensions in humid environments.
               There  exist  more  than  50  types  of  carbon  fibers  with  a  broad  spectrum  of
             strength, stiffness and cost, and the process of fiber advancement is not over - one
             may expect fibers with strength up to 10 GPa and modulus up to 1000 GPa within a
             few years.
               Organic fibers commonly encountered in textile applications can be employed as
             reinforcing elements of  advanced composites.  Naturally,  only  high  performance
             fibers, i.e. fibers possessing high stiffness and strength, can be used for this purpose.
             The most widely used organic fibers that satisfy these requirements are known as
             aramid  (aromatic polyamide) fibers. They  are extruded from a  liquid crystalline
             solution of the corresponding polymer in sulfuric acid with subsequent washing in a
             cold water bath  and stretching under heating. Properties of typical aramid fibers
             are listed in Table 1.1, and the corresponding stress-strain  diagram is presented in
             Fig.  I .7.  As  components  of  advanced  composites for  engineering  applications,
             aramid  fibers are characterized with low  density providing high specific strength
             and  stiffness,  low  thermal  conductivity  resulting  in  high  heat  insulation,  and
             negative thermal expansion coefficient allowing us to construct hybrid composite
             elements that do not change their dimensions under heating. Consisting actually of
             a  system of  very  thin  filaments (fibrils), aramid  fibers have very  high  resistance
             to  damage.  Their  high  strength  in  longitudinal  direction  is  accompanied with
             relatively low  strength  under  tension  in  transverse direction.  Aramid  fibers  are
             characterized with pronounced temperature (see Fig.  1.8) and time dependence for
             stiffness and strength. Unlike inorganic fibers discussed above, they absorb water
             resulting in moisture content up to 7% and degradation of material properties by
             15-20%.
               The  list  of  organic  fibers  was  supplemented  recently  with  extended  chain
             polyethylene fibers demonstrating outstanding low density (less than that of water)
             in  conjunctions  with  relatively  high  stiffness and  strength  (see  Table 1.1  and
             Fig.  1.7). Polyethylene fibers are extruded from the corresponding polymer melt in
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