MMT Clay (mmt + clay)

Distribution by Scientific Domains


Selected Abstracts


Mechanical and morphological properties of organic,inorganic, hybrid, clay-filled, and cyanate ester/siloxane toughened epoxy nanocomposites

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007
S. Nagendiran
Abstract Organic,inorganic hybrids involving cyanate ester and hydroxyl-terminated polydimethylsiloxane (HTPDMS) modified diglycidyl ether of bisphenol A (DGEBA; epoxy resin) filled with organomodified clay [montmorillonite (MMT)] nanocomposites were prepared via in situ polymerization and compared with unfilled-clay macrocomposites. The epoxy-organomodified MMT clay nanocomposites were prepared by the homogeneous dispersion of various percentages (1,5%), and the resulting homogeneous epoxy/clay hybrids were modified with 10% HTPDMS and ,-aminopropyltriethoxysilane as a coupling agent in the presence of a tin catalyst. The siliconized epoxy/clay prepolymer was further modified separately with 10% of three different types of cyanate esters, namely, 4,4,-dicyanato-2,2,-diphenylpropane, 1,1,-bis(3-methyl-4-cyanatophenyl) cyclohexane, and 1,3-dicyanato benzene, and cured with diaminodiphenylmethane as a curing agent. The reactions during the curing process between the epoxy, siloxane, and cyanate were confirmed by Fourier transform infrared analysis. The results of dynamic mechanical analysis showed that the glass-transition temperatures of the clay-filled hybrid epoxy systems were lower than that of neat epoxy. The data obtained from mechanical studies implied that there was a significant improvement in the strength and modulus by the nanoscale reinforcement of organomodified MMT clay with the matrix resin. The morphologies of the siloxane-containing, hybrid epoxy/clay systems showed heterogeneous character due to the partial incompatibility of HTPDMS. The exfoliation of the organoclay was ascertained from X-ray diffraction patterns. The increase in the percentage of organomodified MMT clay up to 5 wt % led to a significant improvement in the mechanical properties and an insignificant decrease in the glass-transition temperature versus the unfilled-clay systems. © 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]


Preparation of extruded melt-mixed polypropylene/montmorillonite nanocomposites with inline monitoring

POLYMER ENGINEERING & SCIENCE, Issue 3 2010
Marcelo K. Bertolino
This article advances the use of an inline optical detector to monitor the disaggregation of the montmorillonite (MMT) clay tactoids during the preparation of polypropylene (PP)/MMT nanocomposites via polymer melt compounding. During the exfoliation of the tactoids their size are reduced below the minimum particle size to produce light extinction and so, the signal of the inline detector reduces as the nanosize composite is formed. The measurement is done at the transient state with the MMT clay added as a pulse with constant weight into the PP extrusion melt flow and followed by the optical detector. The data comes out as the common residence time distribution curves having its maximum intensity related to the tactoids average particle size, keeping all other variables constants. The light extinction was measured for composites with different clays (Cloisite® 15A, 30B, Na+, and Sintered 20A) using the same PP grafted with maleic anhydride compatibilizer. The dissaglomeration/exfoliation efficiency increases as: ,,Sintered 20A'' < ,,Na+ clay'' < ,,organo-modified clay'' < ,,organo-modified clay + compatibilizer''. The best result is obtained using Cloisite® 15A and Cloisite® 20A following the expected reduction of the particle size obtained during a nanocomposite melt processing. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers [source]


Thermo-Mechanical Degradation of LDPE-Based Nanocomposites

MACROMOLECULAR MATERIALS & ENGINEERING, Issue 7 2007
Nadka Tzankova Dintcheva
Abstract Thermo-mechanical degradation of LDPE-based nanocomposites was studied by mainly investigating the rheological properties. For all of the investigated processing conditions, the viscosity of the nanocomposites was higher than that of the pure-LDPE matrix, but on increasing the severity of the mixing conditions, the difference between the viscosity of the nano-filled polymer and that of the pure LDPE decreased. The X-ray traces of the nanocomposites suggest that intercalation has been achieved during the melt, when less-severe processing conditions were used. At severe processing conditions (longer mixing time, high temperature and shear stress) the thermo-mechanical degradation was accelerated, possibly due to the loss of mass from the organoclay galleries. The variations of the viscosity in the presence of two organo-modified montmorillonite (MMt) clays were compared to the ones observed with a MMt clay at different processing conditions. [source]