Home  About us  Contact
 

Resultant Nanocomposites (resultant + nanocomposite)

Distribution by Scientific Domains
Polymers and Materials Science100%

Selected Abstracts

High Mechanical Performance Composite Conductor: Multi-Walled Carbon Nanotube Sheet/Bismaleimide Nanocomposites

ADVANCED FUNCTIONAL MATERIALS, Issue 20 2009
Qunfeng Cheng
Abstract Multi-walled carbon nanotube (MWNT)-sheet-reinforced bismaleimide (BMI) resin nanocomposites with high concentrations (,60,wt%) of aligned MWNTs are successfully fabricated. Applying simple mechanical stretching and prepregging (pre-resin impregnation) processes on initially randomly dispersed, commercially available sheets of millimeter-long MWNTs leads to substantial alignment enhancement, good dispersion, and high packing density of nanotubes in the resultant nanocomposites. The tensile strength and Young's modulus of the nanocomposites reaches 2,088,MPa and 169,GPa, respectively, which are very high experimental results and comparable to the state-of-the-art unidirectional IM7 carbon-fiber-reinforced composites for high-performance structural applications. The nanocomposites demonstrate unprecedentedly high electrical conductivity of 5,500,S cm,1 along the alignment direction. Such unique integration of high mechanical properties and electrical conductance opens the door for developing polymeric composite conductors and eventually structural composites with multifunctionalities. New fracture morphology and failure modes due to self-assembly and spreading of MWNT bundles are also observed. [source]

Photopolymerization of clay/polyurethane nanocomposites induced by intercalated initiator

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2007
Hailin Tan
Abstract An intercalated initiator was synthesized and used for preparation of clay/polyurethane nanocomposites by UV irradiation. Organoclays containing initiator groups were prepared by cationic exchange process which acted as both suitable intercalant and photoinitiator. These modified clays were then dispersed in the mixture of urethane acrylate and hexanediol diacrylate in different loading, then situ photopolymerized. Intercalated and exfoliated nanocomposite structure were evidenced by both X-ray diffraction spectroscopy and Transmission Electron Microscope. Thermal properties and morphologies of the resultant nanocomposites were also investigated. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source]

Clay-PMMA Nanocomposites by Photoinitiated Radical Polymerization Using Intercalated Phenacyl Pyridinium Salt Initiators

MACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 9 2006
Alper Nese
Abstract Summary: In situ synthesis of poly(methyl methacrylate) (PMMA) nanocomposites by photopolymerization using organophilic montmorillonite (MMT) as the layered clay is reported. MMT clay was ion exchanged with N -phenacyl, N,N -dimethylanilinium hexafluoro phosphate (PDA) which acts as both suitable intercalant- and photo-initiator. These modified clays were then dispersed in methyl methacrylate (MMA) monomer in different loading degrees to carry out the in situ photopolymerization. Intercalation ability of the photoinitiator and exfoliated nanocomposite structure were evidenced by both X-ray diffraction (XRD) spectroscopy and transmission electron microscopy (TEM). Thermal properties and morphologies of the resultant nanocomposites were also studied. Schematic representation of clay-PMMA nanocomposites by photoinitiated radical polymerization. [source]

Completely discontinuous organic/ inorganic hybrid nanocomposites by self-curing of nanobuilding blocks constructed from reactions of [HMe2SiOSiO1.5]8 with vinylcyclohexene

POLYMER INTERNATIONAL, Issue 11 2007
Norihiro Takamura
Abstract The reaction of 4-vinyl-1-cylcohexene with [HMe2SiOSiO1.5]8 provides tetra- and octa-2-cyclohexenylethyloctasilsesquioxanes. The tetrabifunctional [cyclohexenylethylMe2SiOSiO1.5]4 -[HMe2SiOSiO1.5]4 (average degree of functionalization) melts near 80 °C and can be cast and then cured (by thermal hydrosilylation) into transparent nanocomposite shapes. These materials, while not nanoporous, offer dielectric constants of 2.8,2.9 at 100 kHz to 3 MHz, and are air stable to temperatures , 400 °C. The resulting materials appear (by X-ray diffraction) to be partially ordered after curing. The octafunctional material also melts at low temperatures (ca 120 °C) and can be copolymerized with hydridosiloxanes to give similar materials with lower thermal stability. The synthesis and characterization of the starting materials is described, as well as thermal curing studies and properties characterization of the resultant nanocomposites. Copyright © 2007 Society of Chemical Industry [source]