4.7 Article

Carbon fiber polypropylene interphase modification as a route to improved toughness

Journal

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.compositesa.2022.107001

Keywords

Carbon Fiber; Polypropylene; Interphase; Interface

Funding

  1. Deakin University [IH210100023, IC160100032, DP180100094, DP220100130]
  2. Deakin University
  3. Australian Government via the ARC Research Hub for Functional and Sustainable Fibres [IH210100023]
  4. ARC Training Centre for Lightweight Automotive Structures and Discovery projects [IC160100032, DP180100094, DP220100130]
  5. Army Research Laboratory and Office of Naval Research [IH210100023, IC160100032]
  6. [FA5209-18-P-0119]
  7. [N62909-18-1-2024]
  8. Australian Research Council [IH210100023] Funding Source: Australian Research Council

Ask authors/readers for more resources

This manuscript presents a rapid surface modification method for carbon fibers using small molecules in polypropylene composites. The attachment of n-butylphenyl species onto the fiber surface improved the toughness by 32% and 30% at 10% and 40% weight fractions respectively. The embedded fiber length, fiber weight fraction, and polymer thermal properties were not affected by the modification, suggesting that the mechanical performance changes originated from the installed surface chemistry blending with the polymer phase.
This manuscript describes the rapid surface modification of carbon fibers using small molecules for application in polypropylene composites at 10% and 40% weight fractions. Attachment of an n-butylphenyl species onto the fiber surface and incorporation into homo-polypropylene resulted in a significant toughness improvement, of 32% and 30% at 10% and 40% weight fractions respectively, when compared against untreated control samples. Further examination of the embedded fiber length, fiber weight fraction, and polymer thermal properties (e.g. Tm and Tc) showed no differences between untreated and treated samples. However, it is proposed that the mechanical performance changes originated from the installed surface chemistry blending with the polymer phase. This is observed through experimental testing which suggests that the sliding interactions of the fiber-matrix interface has created a material that possesses superior ductility and toughness.

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