A simple method was used to assemble single-walled carbon nanotubes into indefinitely long ribbons and fibers. The processing consists of dispersing the nanotubes in surfactant solutions, recondensing the nanotubes in the flow of a polymer solution to form a nanotube mesh, and then collating this mesh to a nanotube fiber. Flow-induced alignment may lead to a preferential orientation of the nanotubes in the mesh that has the form of a ribbon. Unlike classical carbon fibers, the nanotube fibers can be strongly bent without breaking. Their obtained elastic modulus is 10 times higher than the modulus of high-quality bucky paper.
We study the phase behavior of single walled carbon nanotubes in aqueous solutions of surfactant molecules or amphiphilic polymers. Homogeneous dispersions can be obtained by using sodium dodecyl sulfate (SDS) in a well-defined concentration range. In contrast, polyvinyl alcohol (PVA) is not efficient at stabilizing the tubes. Carbon nanotubes stick with each other when PVA is added to homogeneous dispersions initially stabilized by SDS. This behavior is the basis of a simple method that we developed to assemble single walled carbon nanotubes into indefinitely long ribbons and fibers. The processing consists of dispersing the nanotubes in SDS solutions, re-condensing the nanotubes in the flow of a PVA solution to form a nanotube mesh, and then collating this mesh to a nanotube fiber. Flow induced alignment may lead to a preferential orientation of the nanotubes in the mesh that has the form of a ribbon. Unlike classical carbon fibers, the nanotube fibers can be strongly bent without breaking. Their obtained elastic modulus is 10 times higher than the modulus of high-quality bucky paper.
The static fatigue of SiC-based fiber bundles and single fibers has been examined in previous papers, with emphasis placed on the analysis of the stress-rupture time data, and on the modelling of delayed failure from slow crack growth. The present paper investigates the oxidation of the fibers during static fatigue, at temperatures in the intermediate temperature range (5001-8001C). Two oxidation-induced phenomena have been evidenced: the formation of a thin silica film at the surface of fibers and the delayed failure of fiber bundles and single filaments. The stress-rupture time data are interpreted with respect to the chemical and structural characteristics of fibers, and to the oxide film growth rate. The structural analysis of the fibers was carried out using scanning electron microscopy and Auger electron spectroscopy. Delayed failure was found to result from slow crack propagation from surface defects, as a result of the consumption of the free carbon at grain boundaries and the local stresses induced by the SiC-SiO 2 transformation at the crack tip. The respective contributions of these phenomena to static fatigue are discussed.
SiC/SiC minicomposites that comprise different pyrocarbon/silicon carbide ((PyC/SiC) n ) multilayered interphases and a tow of SiC fibers (Hi-Nicalon) have been prepared via pressure-pulsed chemical vapor infiltration. Pyrocarbon and SiC were deposited from propane and a CH 3 SiCl 3 /H 2 mixture, respectively. The microstructure of the interphases has been investigated using transmission electron microscopy. The mechanical tensile behavior of the minicomposites at room temperature exhibits the classical features of tough composites, regardless of the characteristics of the (PyC/SiC) sequences. The interfacial shear stress has been determined from the width of hysteresis loops upon unloading/reloading and from the crack-spacing distance at saturation. All the experimental data indicate that the strength of the fiber/interphase interfaces is rather weak (∼50 MPa).
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