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Montmorillonite polymerization

Organo-modified montmorillonite Polymeric nanocomposites Polymerization Sol-gel technologies... [Pg.65]

Nylon-6. Nylon-6—clay nanometer composites using montmorillonite clay intercalated with 12-aminolauric acid have been produced (37,38). When mixed with S-caprolactam and polymerized at 100°C for 30 min, a nylon clay—hybrid (NCH) was produced. Transmission electron microscopy (tern) and x-ray diffraction of the NCH confirm both the intercalation and molecular level of mixing between the two phases. The benefits of such materials over ordinary nylon-6 or nonmolecularly mixed, clay-reinforced nylon-6 include increased heat distortion temperature, elastic modulus, tensile strength, and dynamic elastic modulus throughout the —150 to 250°C temperature range. [Pg.329]

Moleculady mixed composites of montmorillonite clay and polyimide which have a higher resistance to gas permeation and a lower coefficient of thermal expansion than ordinary polyimides have been produced (60). These polyimide hybrids were synthesized using montmorillonite intercalated with the ammonium salt of dodecylamine. When polymerized in the presence of dimethyl acetamide and polyamic acid, the resulting dispersion was cast onto glass plates and cured. The cured films were as transparent as polyimide. [Pg.330]

NR, styrene-butadiene mbber (SBR), polybutadiene rubber, nitrile mbber, acrylic copolymer, ethylene-vinyl acetate (EVA) copolymer, and A-B-A type block copolymer with conjugated dienes have been used to prepare pressure-sensitive adhesives by EB radiation [116-126]. It is not necessary to heat up the sample to join the elastomeric joints. This has only been possible due to cross-linking procedure by EB irradiation [127]. Polyfunctional acrylates, tackifier resin, and other additives have also been used to improve adhesive properties. Sasaki et al. [128] have studied the EB radiation-curable pressure-sensitive adhesives from dimer acid-based polyester urethane diacrylate with various methacrylate monomers. Acrylamide has been polymerized in the intercalation space of montmorillonite using an EB. The polymerization condition has been studied using a statistical method. The product shows a good water adsorption and retention capacity [129]. [Pg.866]

E. Haque. Physicochemical interactions between montmorillonite and polymerizing systems Effect on particle-reinforced composites. PhD thesis. Rice Univ, 1986. [Pg.401]

The authors [1] studied kinetics of poly (amic acid) (PAA) solid phase imidization in the presence of nanofiller (Na+-montmorillonite) and in its absence. It was found out, that the kinetic curves conversion (imidization) degree Q versus reaction duration t were have typical for polymerization reactions shape with autodeceleration showing imidization rate reduction as time is passing. As it is known [2], such curves Q(t) are specific for reaction passing in heterogeneous medium and are described by the simple relationship ... [Pg.223]

Soma et al. (12) have generalized the trends for aromatic compound polymerization as follows (1) aromatic compounds with ionization potentials lower than approximately 9.7 eV formg radical cations upon adsorption in the interlayer of transition-metal ion-exchanged montmorillonites, (2) parasubstituted benzenes and biphenyls are sorbed as the radical cations and prevented from coupling reactions due to blockage of the para position, (3) monosubstituted benzenes react to 4,4 -substituted biphenyls which are stably sorbed, (4) benzene, biphenyl, and p-terphenyl polymerized, and (5) biphenyl methane, naphthalene, and anthracene are nonreactive due to hindered access to reaction sites. However, they observed a number of exceptions that did not fit this scheme and these were not explained. [Pg.471]

J. Zhang, L. Wang, A. Wang, Preparation and properties of chitosan-g-poly(acrylic acid)/montmorillonite superabsorbent nanocomposite via In situ intercalative polymerization, Ind. Eng. Chem Res., vol. 46, pp. 2497-2505, 2007. [Pg.115]

Styrene Polymerization Palygorskite, kaoUnite, and montmorillonite Weakest catalyst is montmorillonite... [Pg.298]

A small increase of the (d 001) basal spacing is observed for the Li containing Zr pillared clays. However, the thermal stability of these solids drastically decrease. At high temperature, the collapse of the strucutre is also supported by the decrease of the surface area which is, at 700°C, almost identical to those measured for the montmorillonite. Different hypothesis may be proposed to explain the increase of the interlayer distance at low temperature (i) a better polymerization of the intercalated complex (ii) a modification of the distribution of the pillars (iii) a lower interaction between the pillar and the silica layer. The first hypothesis may easily be eliminated since the small variation of the height of the pillars (less than 1 A) cannot be explained by structural changes of the... [Pg.101]

The presence of an organophilic clay increases the catalyst activity (10). Suitable clays include montmorillonite, hectorite, mica, etc. For example, Lucentite is a trioctylmonomethylammonium salt-treated synthetic hectorite. The clays are modified with quaternary ammonium compounds. The clays are heat treated prior to their use in the polymerization process. Further, the incorporated clay can improve the performance of the UHMWPE or function as filler. [Pg.80]

Low-loaded, organophilic Pd-montmorillonites were shown to exhibit high cis-selectivity in the hydrogenation of 1-phenyl-1-alkynes working with high (=5000) substrate catalyst ratio.402 Studies with respect to the use palladium membrane catalysts403 105 and polymeric hollow fiber reactors406"408 were reported. [Pg.671]

Oxidizing/Reducing Entities. Other reactions depend on oxidation/reduction processes. Among them is polymerization of various aromatic molecules. Such polymerizations are preceeded by formation of radical cations of the aromatic hydrocarbon. Cu-montmorillonites are capable of catalyzing such reactions (136). [Pg.20]

Leszczynska, A., Njuguna, J., Pielichowski, K., and Banerjee, J. R. (a) Polymer/montmorillonite nanocomposites with improved thermal properties, Part I Factors influencing thermal stability and mechanisms of thermal stability improvement, Thermochim. Acta (2007), 453, 75-96. (b) Polymer/montmorillonite nanocomposites with improved thermal properties. Part II Thermal stability of montmorillonite nanocomposites based on different polymeric matrixes, Thermochim. Acta (2007), 454, 1-22. [Pg.292]


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