Magnetic alignment of SWCNTs decorated with Fe3O4 to enhance mechanical properties of SC-15 epoxy
Source abstract
Abstract
We report significant improvement in mechanical properties of SC-15 epoxy when reinforced with decorated nanotubes and cured in a modest magnetic field. The chemical synthesis and field curing process is a low cost and relatively easy technique to impose strong magnetic anisotropy into the system without the need of a superconducting magnet. SWCNT(COOH)s were decorated with Fe3O4nanoparticles through a sonochemical oxidation process and then dispersed into SC-15 epoxy at 0.5 wt% loading. The admixture was cured for 6 hours in a magnetic field of 10 kOe followed by an additional 24 hours of post curing at room temperature. Control samples were prepared in a similar manner but without the application of the magnetic field. Mechanical tests performed on field-cured samples indicated that tensile strength and modulus increased by 62%and 40%. Most importantly, modulus of toughness, fracture strain, and modulus of resilience improved by 346%, 165%% and 170%, respectively. Such enhancement in mechanical properties was attributed to changes in polymer morphology, partial alignment of nanotubes in the field direction, and sliding at the polymer-nanotube interface. Detailed characterization of the system with XRD, TEM, DMA, and Magnetometry are described in the paper.
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Research context
OpenAlex topics: Carbon Nanotubes in Composites · Polymer Nanocomposites and Properties · Fiber-reinforced polymer composites
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Florida Atlantic University 1 Department of Ocean and Mechanical Engineering, , Boca Raton, Florida 33431, USA
Florida Atlantic University 2 Department of Physics, , Boca Raton, Florida 33431, USA
Oak Ridge National Laboratory 3 Center for Nanophase Materials Sciences, , Oak Ridge, Tennessee 37831, USA
Tuskegee University 4 Center for Advanced Materials (T-CAM), , Tuskegee, Alabama 36088, USA
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