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Clay/polyurethane Nanocomposites (polyurethane + nanocomposite)

Distribution by Scientific Domains

Polymers and Materials Science	100%

Selected Abstracts

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]

Thermal stability and molecular interaction of polyurethane nanocomposites prepared by in situ polymerization with functionalized multiwalled carbon nanotubes

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008
R. N. Jana
Abstract Polyurethane (PU) nanocomposites were prepared through conventional and in situ methods with multiwalled carbon nanotubes (MWNTs) functionalized with poly(,-caprolactone). The thermal degradation and stability of PU,MWNT nanocomposites were investigated with nonisothermal thermogravimetry and were explained in terms of the interaction between MWNTs and PU molecules with Fourier transform infrared spectroscopy. The difference in thermal stability between the conventional and in situ nanocomposites was also compared. The thermal degradation of all the nanocomposite samples took place in two stages and followed a first-order reaction. The degradation temperature of the in situ nanocomposites was higher than that of the conventional nanocomposites with the same loading of MWNTs. The activation energy at 10% degradation and the half-life period were also higher in the in situ nanocomposites compared to the conventional nanocomposites. Such higher thermal stability of the in situ nanocomposites was ascribed to covalent bond formation between MWNTs and PU chains, which could result in better dispersion of MWNTs in the PU matrix for the in situ nanocomposites than for the conventional nanocomposites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]

Effective preparation and characterization of montmorillonite/poly(,-caprolactone)-based polyurethane nanocomposites

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2008
Eun Hwan Jeong
Abstract In this study, montmorillonite (MMT)/poly(,-caprolactone)-based polyurethane cationomer (MMT/PCL-PUC) nanocomposites were prepared and their mechanical properties, thermal stability, and biodegradability were investigated. PCL-PUC has 3 mol % of quaternary ammonium groups in the main chain. The MMT was successfully exfoliated and well dispersed in the PCL-PUC matrix for up to 7 wt % of MMT. The 3 mol % of quaternary ammonium groups facilitated exfoliation of MMT. The 1 wt % MMT/PCL-PUC nanocomposites showed enhanced tensile properties relative to the pure PCL-PU. As the MMT content increased in the MMT/PCL-PUC nanocomposites, the degree of microphase separation of PCL-PUC decreased because of the strong interactions between the PCL-PUC chains and the exfoliated MMT layers. This resulted in an increase in the Young's modulus and a decrease in the elongation at break and maximum stress of the MMT/PCL-PUC nanocomposites. Biodegradability of the MMT/PCL-PUC nanocomposites was dramatically increased with increasing content of MMT, likely because of the less phase-separated morphology of MMT/PCL-PUC. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]

Morphological and physical properties of a thermoplastic polyurethane reinforced with functionalized graphene sheet

POLYMER INTERNATIONAL, Issue 4 2009
Duc Anh Nguyen
Abstract BACKGROUND: Functionalized graphene sheet (FGS) was recently introduced as a new nano-sized conductive filler, but little work has yet examined the possibility of using FGS as a nanofiller in the preparation of polymer nanocomposites. In particular, there are currently no published papers that evaluate polyurethane/FGS nanocomposites. The purpose of this study was to prepare a polyurethane/FGS nanocomposite and examine the morphological and physical properties of the material. RESULTS: A cast nanocomposite film was prepared from a mixture of thermoplastic polyurethane (TPU) solution and FGS suspended in methyl ethyl ketone. The FGS dispersed on the nanoscale throughout the TPU matrix and effectively enhanced the conductivity. A nanocomposite containing 2 parts of FGS per 100 parts of TPU had an electrical conductivity of 10,4 S cm,1, a 107 times increase over that of pristine TPU. The dynamic mechanical properties showed that the FGS efficiently reinforced the TPU matrix, particularly in the temperature region above the soft segment melt. CONCLUSION: Our results show that FGS has a high affinity for TPU, and it could therefore be used effectively in the preparation of TPU/FGS nanocomposites without any further chemical surface treatment. This indicates that FGS is an effective and convenient new material that could be used for the modification of polyurethane. It could also be used in place of other nano-sized conductive fillers, such as carbon nanotubes. Copyright © 2009 Society of Chemical Industry [source]

Preparation and properties of polyurethane/montmorillonite nanocomposites cured under room temperature

POLYMER COMPOSITES, Issue 5 2006
Hangbin Jiang
The polyurethane/C16C18 -MMT (the montmorillonite modified with cetyloctadecyldimethyl ammonium bromide) nanocomposites were synthesized by intercalative polymerization and cured under room temperature. The d -spacing and the dispersion of the C16C18 -MMT in the nanocomposites were measured by X-ray Diffraction (XRD) and Transmission Electron Microscope (TEM). The mechanical and thermal properties of the nanocomposites were measured by Universal Testing System, Electric Anti-fold Instrument, Thermogravimetric Analysis (TGA), and Differential Scanning Calorimetry (DSC). It was found out that introducing C16C18 -montmorillonite (MMT) in the polyurethane (PU) displayed good mechanical properties and thermal stability. Rheology behavior in liquid state showed that the addition of the C16C18 -MMT to PU resulted in low gel time and high viscosity. POLYM. COMPOS. 27:470,474, 2006. © 2006 Society of Plastics Engineers. [source]