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Effect of nanotube functionalization on the properties of single‐walled carbon nanotube/polyurethane composites
Authors:Fabian Buffa  Gustavo A. Abraham  Brian P. Grady  Daniel Resasco
Affiliation:1. Instituto de Investigaciones en Ciencia y Tecnología de Materiales, INTEMA (UNMdP‐CONICET), Av. J. B. Justo 4302, B7608FDQ Mar del Plata, Argentina;2. School of Chemical, Biological and Materials Engineering and Carbon Nanotube Technology Center (CANTEC), University of Oklahoma, 100 East Boyd, Norman, Oklahoma 73019School of Chemical, Biological and Materials Engineering and Carbon Nanotube Technology Center (CANTEC), University of Oklahoma, 100 East Boyd, Norman, Oklahoma 73019;3. School of Chemical, Biological and Materials Engineering and Carbon Nanotube Technology Center (CANTEC), University of Oklahoma, 100 East Boyd, Norman, Oklahoma 73019
Abstract:A commercially available aliphatic thermoplastic polyurethane formulated with a methylene bis(cyclohexyl) diisocyanate hard segment and a poly(tetramethylene oxide) soft segment and chain‐extended with 1,4‐butanediol was dissolved in dimethylformamide and mixed with dispersed single‐walled carbon nanotubes. The properties of composites made with unfunctionalized nanotubes were compared with the properties of composites made with nanotubes functionalized to contain hydroxyl groups. Functionalization almost eliminated the conductivity of the tubes according to the conductivity of the composites above the percolation threshold. In most cases, functionalized and unfunctionalized tubes yielded composites with statistically identical mechanical properties. However, composites made with functionalized tubes did have a slightly higher modulus in the rubbery plateau region at higher nanotube fractions. Small‐angle X‐ray scattering patterns indicated that the dispersion reached a plateau in the unfunctionalized composites that was consistent with the plateau in the rubbery plateau region. The room‐temperature modulus and tensile strength increase was proportionally higher than almost all increases seen previously in thermoplastic polyurethanes; however, the increase was still an order of magnitude below what has been reported for the best nanotube–polymer systems. Nanotube addition increased the hard‐segment glass transition temperature slightly, whereas the soft‐segment glass transition was so diffuse that no conclusions could be drawn. Unfunctionalized tubes suppressed the crystallization of the hard segment; whereas functionalized tubes had no effect. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 490–501, 2007
Keywords:crystallization  glass transition  nanocomposites  polyurethanes  segmented polyurethanes  SAXS  single‐walled carbon nanotubes
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