Microstructure and elastic properties of individual components of C/C composites

Soydan Ozcan, Jale Tezcan, Peter Filip

Research output: Contribution to journalArticlepeer-review

64 Scopus citations

Abstract

Carbon fiber reinforced carbon matrix (C/C) composites are often used for structural and frictional applications at a wide range of temperatures due to their excellent mechanical and thermal properties. Tailoring of mechanical properties through optimization of microstructure is critical for achieving maximum composite performance. This article addresses the evolution of the fiber and matrix microstructure and related nano-mechanical properties in two different C/C composites after being subjected to heat treatment at temperatures between 1800 and 2400 °C. Microstructure and corresponding nano-mechanical properties of C/C composites were studied using Polarized Light Microscopy (PLM), High-Resolution Transmission Electron Microscopy (HRTEM) and nanoindentation techniques. Increased heat treatment temperature (HTT) led to formation of a better-organized microstructure of fiber and matrix and also to formation of thermal cracks. The elastic modulus of rough laminar CVI pyrocarbon decreased from 18 to 12 GPa with increased HTT. In contrast, the isotropic CVI pyrocarbon and charred resin matrix displayed only a slight change of elastic modulus. The elastic modulus of PAN fiber increased from 18 to 34 GPa, indicating the development of a better-organized microstructure in the fiber-axial direction.

Original languageEnglish
Pages (from-to)3403-3414
Number of pages12
JournalCarbon
Volume47
Issue number15
DOIs
StatePublished - Dec 2009
Externally publishedYes

Funding

This research was sponsored by the National Science Foundation (Grant EEC 3369523372), State of Illinois and a consortium of 11 industrial partners of Center for Advanced Friction Studies ( http://frictioncenter.engr.siu.edu ). The authors acknowledge Mr. Bijay Gurung for his help on nanoindentation studies, and Drs. John Bozzola and Steve Schmitt at Micro-imaging and Analysis Center at Southern Illinois University for assisting with the microscopy studies. The high-resolution TEM characterization was carried out at the Center for Microanalysis of Materials, University of Illinois, which is partially supported by the US Department of Energy under Grant DEFG02-91-ER45439.

FundersFunder number
State of Illinois
National Science FoundationEEC 3369523372
U.S. Department of EnergyDEFG02-91-ER45439

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