Nanoclay Loadings (nanoclay + loading)

Distribution by Scientific Domains


Selected Abstracts


Effects of nano- and micro-fillers and processing parameters on injection-molded microcellular composites

POLYMER ENGINEERING & SCIENCE, Issue 6 2005
Mingjun Yuan
The effects of submicron core-shell rubber (CSR) particles, nanoclay fillers, and molding parameters on the mechanical properties and cell structure of injection-molded microcellular polyamide-6 (PA6) composites were studied. The experimental results of PA6 nanocomposites with 5.0 and 7.5 wt% nanoclay loadings and of CSR-modified PA6 composites with 0.5 and 3.1 wt% CSR loadings were compared to their neat resin counterparts. This study found that nanoclay was more efficient in promoting a smaller cell size, larger cell density, and higher tensile strength for microcellular injection molding parts. A higher nanoclay loading led to more brittle behavior for microcellular parts. It was found that a proper amount of CSR particles could be added to the microcellular injection-molded PA6 to reduce the cell size, increase the cell density, and enhance the toughness of the molded part. However, CSR particles were less effective cell nucleation agents as compared to nanoclay for producing desirable cell structures, and a higher CSR loading was found to have diminishing effects on the process and on the properties of the parts. POLYM. ENG. SCI., 45:773,788, 2005. © 2005 Society of Plastics Engineers [source]


Correlation of morphology, rheology, and performance improvement in gasoline tubes based on PA-6 nanocomposites

JOURNAL OF VINYL & ADDITIVE TECHNOLOGY, Issue 3 2010
Mehdi Moghri
PA-6/organo-modified layered silicate nanocompounds were prepared by the melt mixing of PA-6 with different nanoclay loadings in a corotating twin-screw extruder. Gasoline tubes based on these nanocompounds were produced at different silicate loadings. Thermal, mechanical, rheological, and barrier properties of the different samples were investigated and correlated to their morphology. Transmission electron microscopy, wide angle X-ray scattering, and linear melt state viscoelastic measurements were used to characterize the different aspects of nanoclay dispersion in the nanocomposite samples. While tensile modulus, softening point, heat distortion temperature, and gasoline barrier properties of the prepared tubes were improved considerably by increasing the clay content, performance improvement with respect to clay content (after a certain value) decreased with increasing clay loading. It could be attributed to the re-agglomeration of tactoids at higher concentrations. These findings were correlated with the rheological and morphological observations. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers [source]


CO2 sorption and diffusion in polymethyl methacrylate,clay nanocomposites

POLYMER ENGINEERING & SCIENCE, Issue 7 2005
Allan R. Manninen
This study reports the glass transition temperature (Tg), and sorption and diffusion of subcritical CO2 gas in polymethyl methacrylate (PMMA) nanocomposites containing organically modified smectite clay, Cloisite 20A (C20A). A range of methods for preparing the PMMA-clay nanocomposites was investigated and a solution coprecipitation method was selected as the most appropriate. Using this method, PMMA nanocomposite containing 2, 4, 6, and 10 wt% nanoclay loadings were prepared. Wide-angle X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM) indicated that the 2 wt% nanocomposite materials had a well-dispersed intercalated clay structure. The Tg for PMMA-C20A nanocomposites, as measured by differential scanning calorimetry (DSC), was found to be independent of the clay loading. CO2 solubility studies from 0 to 65°C and pressures up to 5.5 MPa using an in situ gravimetric technique were performed on compression-molded films. The organoclay was found to have no effect on the solubility of CO2 in PMMA, and therefore the solubility of CO2 in the nanocomposite can be determined from the solubility of CO2 in the matrix polymer alone. Diffusion coefficients were determined using the appropriate transport models for these test conditions and the diffusion coefficients for CO2 in PMMA-C20A composites were found to increase with organoclay loading. It is believed that the processing path taken to prepare the nanocomposites may have resulted in the agglomeration of the C20A organoclay, thereby preventing the polymer chains from fully wetting and intercalating a large number of clay particles. These agglomerations are responsible for the formation of large-scale holes within the glassy nanocomposite, which behave as low resistance pathways for gas transport within the PMMA matrix. POLYM. ENG. SCI., 45:904,914, 2005. © 2005 Society of Plastics Engineers [source]


Effects of nano- and micro-fillers and processing parameters on injection-molded microcellular composites

POLYMER ENGINEERING & SCIENCE, Issue 6 2005
Mingjun Yuan
The effects of submicron core-shell rubber (CSR) particles, nanoclay fillers, and molding parameters on the mechanical properties and cell structure of injection-molded microcellular polyamide-6 (PA6) composites were studied. The experimental results of PA6 nanocomposites with 5.0 and 7.5 wt% nanoclay loadings and of CSR-modified PA6 composites with 0.5 and 3.1 wt% CSR loadings were compared to their neat resin counterparts. This study found that nanoclay was more efficient in promoting a smaller cell size, larger cell density, and higher tensile strength for microcellular injection molding parts. A higher nanoclay loading led to more brittle behavior for microcellular parts. It was found that a proper amount of CSR particles could be added to the microcellular injection-molded PA6 to reduce the cell size, increase the cell density, and enhance the toughness of the molded part. However, CSR particles were less effective cell nucleation agents as compared to nanoclay for producing desirable cell structures, and a higher CSR loading was found to have diminishing effects on the process and on the properties of the parts. POLYM. ENG. SCI., 45:773,788, 2005. © 2005 Society of Plastics Engineers [source]