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New polyurethane nanocomposites preparation, structure and properties of
Author: GuoShuZhong
Tutor: LiuTianXi
School: Fudan University
Course: Polymer Chemistry and Physics
Keywords: Nanocomposites Multi-walled carbon nanotubes Layered double hydroxides Fudan University Structure and Properties Polyurethane Elastomer Elongation at break Polysiloxane Isocyanate
CLC: TB383.1
Type: Master's thesis
Year: 2009
Downloads: 343
Quote: 1
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Abstract
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Polyurethane (PU) elastomers are a cross between rubber and plastic elastic material, with both high elasticity of rubber, but also has a high-strength plastic. Its wear resistance, biocompatibility and blood compatibility particular. It also has excellent oil resistance, impact resistance, low temperature resistance, ozone resistance, radiation resistance and weight-bearing insulation, and insulation. As superior overall performance and is widely used in civil, sports, aerospace, military and other fields, to become an important and indispensable materials. But because of its strength, biocompatibility, heat and oxidation performance is also not ideal, its application is limited to a certain extent. To further broaden its application field, researchers usually some nanoparticles added to the system to improve the performance of some of the polyurethane material. In this paper, the polyester polyol (PDA), isophorone diisocyanate (IPDI), isophorone diamine (IPDA) system, the prepolymer prepared using three different polyurethane nanocomposite system, and structure and properties were studied in detail, the main research results obtained are as follows: (1) a combination of in-situ polymerization and solution casting method to prepare polyurethane / multi-walled carbon nanotubes (MWNT) composite materials. As can be seen by scanning electron microscopy, when the low levels of carbon uniformly dispersed in the polyurethane tube in the body, and the carbon nanotubes between the polymer body and the carbon nanotubes have a strong interfacial interaction force (by the embedded in the polyurethane matrix is ??pulled off the morphology of carbon nanotubes), which is conducive to the stress transmitted from the polymer to the carbon tube body, while maintaining a high elongation at break under the premise of having excellent mechanical successfully prepared nanocomposite tensile strength, and this The thermal stability is also improved significantly. (2) synthesized by RAFT polymerization of a range of different molecular weights of PU-b-PTPM (PTPM, poly [3 - (trimethoxysilyl) propyl acrylate]) amphiphilic block copolymers, such copolymers in THF / methanol mixed solvent can self-assemble into the shell with PU to hydrophobic PTPM for the nuclear nuclear - shell structure, and then through the hydrolysis and condensation catalyst synthesis PU / silsesquioxane ball nanocomposites. By the tensile test, TGA and atomic force microscopy study found that compared to pure polyurethane resin, the mechanical properties of the resulting composite material properties and thermal stability were significantly increased; and with the block polymer molecular weight increase, an increasing number of available , the size of uniform silsesquioxane nanoparticles. (3) dodecyl sulfonate anions CoAl-layered double hydroxide (LDH) for intercalation and were first prepared by in situ polymerization of exfoliated polyurethane / CoAl-LDH nanocomposites. Using X-ray diffraction, tensile test, thermal gravimetric analysis, real-time Fourier transform infrared spectroscopy by means of nanocomposite structure / morphology, mechanical properties, thermal stability, and found that its thermal oxidation and mechanical performance was significantly better than the pure polyurethane resin.
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