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Montmorillonite Nanocomposites (montmorillonite + nanocomposite)

Distribution by Scientific Domains

Polymers and Materials Science	100%

Selected Abstracts

Synthesis and characterization of poly(styrene-maleic anhydride)-montmorillonite nanocomposite

POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 5 2002
N. Salahuddin
Abstract Poly(styrene-maleic anhydride)-montmorillonite nanocomposites were prepared by intercalation of layered montmorillonite with the polymer ions. Synthetic approaches including polymerization and phosphonium salt formation have been used for polymer intercalation and dispersion of the host layers in the polymer matrix. The ratio of the mineral in the composites ranged 30,50%. Wide-angle X-ray diffraction (WAXD) disclosed that the d(001) spacing between the internal lamellar surface were only expanding to about 13 and 15,Å according to the type of phosphonium salt suggesting packing of polymer molecules between the layers. Examination of these materials by scanning and transmission electron microscopy showed spherical nano size particles of average diameter, 350,nm. Copyright © 2002 John Wiley & Sons, Ltd. [source]

Thermal degradation kinetics of epoxy/organically modified montmorillonite nanocomposites

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008
Ivan Brnardi
Abstract Nanocomposites based on a commercial epoxy resin and organically modified montmorillonites (OMMTs), containing 5 and 10 phr OMMT, were prepared and characterized. Poly(oxypropylene) diamine (Jeffamine D400) and octadecylamine were used as organic modifiers. Another poly(oxypropylene) diamine (Jeffamine D230) was used as a curing agent. The thermal degradation kinetics of the neat resin system and nanocomposites were investigated by thermogravimetric analysis. The dispersion of silicate layers within the crosslinked epoxy matrix was verified by transmission electron microscopy. The activation energy of degradation for the investigated systems was determined by the isoconversional Kissinger,Akahira,Sunose method. The thermal behavior of the neat resin systems and nanocomposites was modeled with an empirical kinetic model. The influence of organic modifiers and the OMMT loading on the thermal stability of the nanocomposites was discussed. © 2007 Wiley Periodicals, Inc. JAppl Polym Sci, 2008 [source]

Synthesis and characterization of novel poly(o -toluidine) montmorillonite nanocomposites: Effect of surfactant on intercalation

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2007
Rahul Singhal
Abstract The investigation of clay based polymer nanocomposites has opened the door for the development of novel, ecofriendly advanced nano materials that can be safely recycled. Because of their nanometer size dispersion, these nanocomposites often have superior physical and mechanical properties. In this study, novel nanocomposites of poly(o -toluidine) (POT) and organically modified montmorillonite (MMT) were synthesized using camphor sulfonic acid (CSA), cetyl pyridinum chloride (CPCl), and N -cetyl- N,N,N -trimethyl ammonium bromide (CTAB) to study the role of surfactant modification on the intercalation. The in situ intercalative polymerization of POT within the organically modified MMT layers was analyzed by FTIR, UV,visible, XRD, SEM as well as TEM studies. The average particle size of the nanocomposites was found to be in the range 80,100 nm. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source]

Recycled PET nanocomposites improved by silanization of organoclays

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007
Milan Krá, alík
Abstract Recycled PET/organo-modified montmorillonite nanocomposites were prepared via melt compounding as a promising possibility of the used beverage bottles recovery. According to our previous work, the three suitable commercial organoclays Cloisite 25A, 10A, and 30B were additionally modified with [3-(glycidyloxy)propyl]trimethoxysilane, hexadecyltrimethoxysilane and (3-aminopropyl)trimethoxysilane. The selected organoclays were compounded in the concentration 5 wt % and their degree of intercalation/delamination was determined by wide-angle X-ray scattering and transmission electron microscopy. Modification of Cloisite 25A with [3-(glycidyloxy)propyl]trimethoxysilane increased homogeneity of silicate layers in recycled PET. Additional modification of Cloisite 10A and Cloisite 30B led to lower level of delamination concomitant with melt viscosity reduction. However, flow characteristics of all studied organoclay nanocomposites showed solid-like behavior at low frequencies. Silanization of commercial organoclays had remarkable impact on crystallinity and melt temperature decrease accompanied by faster formation of crystalline nuclei during injection molding. Thermogravimetric analysis showed enhancement of thermal stability of modified organoclays. The tensile tests confirmed significant increase of PET-R stiffness with organoclays loading and the system containing Cloisite 25A treated with [3-(glycidyloxy)propyl]trimethoxysilane revealed combination of high stiffness and extensibility, which could be utilized for production of high-performance materials by spinning, extrusion, and blow molding technologies. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source]

Morphology and mechanical and viscoelastic properties of rubbery epoxy/organoclay montmorillonite nanocomposites

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2007
Amar Boukerrou
Abstract The morphology and mechanical and viscoelastic properties of rubbery epoxy/organoclay montmorillonite (MMT) nanocomposites were investigated with wide-angle X-ray scattering (WAXS), transmission electron microscopy (TEM), tensile testing, and dynamic mechanical thermal analysis. An ultrasonicator was used to apply external shearing forces to disperse the silicate clay layers in the epoxy matrix. The first step of the nanocomposite preparation consisted of swelling MMT in a curing agent, that is, an aliphatic diamine based on a polyoxypropylene backbone with a low viscosity for better diffusion into the intragalleries. Then, the epoxy prepolymer was added to the mixture. Better dispersion and intercalation of the nanoclay in the matrix were expected. The organic modification of MMT with octadecylammonium ions led to an increase in the initial d -spacing (the [d001] peak) from 14.4 to 28.5 Å, as determined by WAXS; this indicated the occurrence of an intercalation. The addition of 5 phr MMTC18 (MMT after the modification) to the epoxy matrix resulted in a finer dispersion, as evidenced by the disappearance of the diffraction peak in the WAXS pattern and TEM images. The mechanical and viscoelastic properties were improved for both MMT and MMTC18 nanocomposites, but they were more pronounced for the modified ones. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 103: 3547,3552, 2007 [source]

Preparation and characterization of polypropylene/solid-state organomodified montmorillonite nanocomposites

POLYMER COMPOSITES, Issue 4 2008
Sun Yu-hai
A novel organomodified montmorillonite prepared by solid-state method and its nanocomposites with polypropylene were studied. The interaction between modifying agent and montmorillonite was investigated by X-ray diffraction (XRD) analysis, contact angle determination, and Fourier-transform infrared spectroscopy. The results showed that the modifying agent behaves as an effective intercalating agent, enlarging the interlayer spacing of montmorillonite and making montmorillonite more hydrophobic. Polypropylene/solid-state organomodified montmorillonite composites were prepared by melt-mixing method. The dispersion of the silicates was investigated by XRD analysis and transmission electron microscopy. It was found that the nanocomposites are formed with solid-state organomodified montmorillonite and polypropylene. The thermogravimetric analysis and differential scanning calorimetry results showed that the organoclay could enhance the thermal stability and decrease the relative crystallinity of polypropylene. Mechanical and rheological tests indicated that the organoclay improves the mechanical properties but has no obvious effect on rheological properties of polypropylene. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers [source]

Synthesis of exfoliated polyamide 6,6/organically modified montmorillonite nanocomposites by in situ interfacial polymerization

POLYMER COMPOSITES, Issue 6 2007
M. Tarameshlou
Polyamide 6,6 (PA 6,6)/organically modified montmorillonite (OMMT) nanocomposites were prepared by a novel method, using direct interfacial polymerization of an aqueous hexamethylene diamine and a nonaqueous adipoyl chloride in dichloromethane solution containing different amounts of OMMT dispersed nanoparticles. The state of dispersion of OMMT in the PA 6,6 matrix was investigated by means of X-ray diffraction, as well as transmission electronic microscopy. The results indicated that the OMMT nanoparticles were dispersed homogeneously and nearly exfoliated in the PA 6,6 matrix. The random arrangement of clay platelets in the PA 6,6 matrix, exfoliation, and intercalation of clays between the PA 6,6 matrix were distinguished. The amount of the incorporated OMMT in the PA 6,6 matrix was determined by means of TGA technique. Furthermore it was found that addition of a small amount of OMMT dramatically improved the thermal stability of PA 6,6. The TGA thermograms of all the synthesized nanocomposite samples showed an interesting unexpected lag in the weight loss at high temperatures, which could be another evidence for formation of fully exfoliated nanocomposites structures, with improved thermal stability. Nucleating effect of the OMMT nanoparticles and their influence on crystallization behavior of PA 6,6 was confirmed by DSC. Finally it is concluded that the in situ interfacial polycondensation is a suitable method for synthesis of nanocomposites with well dispersed structures and enhanced properties. POLYM. COMPOS., 28:733,738, 2007. © 2007 Society of Plastics Engineers [source]