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Trimethylammonium methacrylate

Cationic water-dissolved polyelectrolytes find wide application in industry different fields, namely, for the ecological problems solution [34]. For understanding these polymers action mechanism and synthesis processes it is necessary to define their molecular characteristics and water solutions properties too [35]. Therefore, the authors [36] performed description of cationic polyelectrolytes in solution behavior within the framework of fractal analysis on the example of copolymer of acrylamide with trimethylammonium methacrylate chloride (PAA-TMAC). The data [35] for four copolymer PAA-TMAC with TMAC contents of 8, 25, 50 and 100 mol. % were used. In Ref [35] the equations Maik-Kuhn-Hou-wink type were obtained, which linked intrinsic viscosity [q] (the Eq. (1)) and macromolecular coil gyration radius with average weight molecular weight of polymer [35] ... [Pg.52]

Poly [ l(2-hydroxyethyl)trimethylammonium methacrylate] benzene sulfonate ... [Pg.2041]

Molecular weights of polymers that function as bridging agents between particles are ca 10 —10. Ionic copolymers of acrylamide are the most significant commercially (see Acrylamide POLYMERS). Cationic comonomers include (2-methacryloyloxyethyl)trimethylammonium salts, diethyl aminoethyl methacrylate [105-16-8], and dimethyldiallylammonium chloride [7398-69-8], anionic comonomers include acryUc acid [79-10-7] and its salts. Both types of polyacrylamides, but especially the anionic, can be more effective in the presence of alum (10,11). Polyetbylenimine and vinylpyridine polymers, eg, po1y(1,2-dimethy1-5-viny1pyridiniiim methyl sulfa te) [27056-62-8] are effective but are used less frequentiy. [Pg.15]

PE-TMAI pentaerythritol trimethylammonium iodide phen 1,10-phenanthroline PMMA poly(methyl methacrylate)... [Pg.258]

PAA = poly (acrylic acid), PMAA = poly(methacrylic acid), PI A = poly(itaconic acid), PGA = poly(L-glutamic acid), QPVP = poly(N-ethyl-4-vinyl-pyridinium bromide), PLL = poly(L-lysine), PDMAEMA = poly(2-N,N-dimethylaminoethyl methacrylate), PVBMA = poly(4-vinylbenzyl-trimethylammonium chloride), 5,6-ionene, 2,5-ionene, 10,10-ionene, 2X and 3X (see text)... [Pg.25]

NaSS = polyfsodium styrenesulfonate), FVBMA = poly(4-vinylbenzyl-trimethylammonium chloride), PAA = poly(acrylic acid), PEPP = poly(ethylenepiperazine), HEMA = poly(2-hyd-roxyethyl methacrylate)... [Pg.42]

As a result, zones A, B, and C have comparatively a basic, neutral, and acidic character, respectively. Increasing the DC electric current leads to the overall acidification of the gel sample (see Fig. 6, curve 4) due to the easy ionization of the acidic groups. Consequently, this narrows the zones B and C and expands zone A. Polybetaine hydrogel membranes of isopropyl-2-[2 -(trimethylammonium)ethyl phosphoryl] ethyl fumaramate and 2-hydroxyethyl methacrylate effectively enhance the water content in comparison with poly(2-hydroxyethyl methacrylate) [224]. The content of water in hydrogel membranes increases, but the amount of adsorbed BSA decreases with the increase of the betaine content in the feed. The values of the tensile strength and tensile elongation of the hydrogel reach 68.4 g mm and 239%, respectively. [Pg.196]

A similar photo-effect on the swelling of cross-linked poly(methacrylic acid) (PMA) was observed in the presence of 4-phenylazophenyl trimethylammonium ions (J9) [38]. An increased cis content of the chromophore by photoirradiation at a pH in the range of conformation unfolding of PMA led to an increased ionization and thus enhanced swelling. The conversion efficiency of light energy to mechanical work was calculated to be 3 x 10 . ... [Pg.46]

General. Aqueous solutions of hydrophilic monomers were emulsified in xylene using water-in-oil emulsifiers, and polymerized using oil-soluble initiators. Typical hydrophilic monomers were sodium p-vinylbenzene sulfonate, sodium vinylbenzyl sulfonate, 2-sulfoethyl acrylate, acrylic acid, acrylamide, vinylbenzyl-trimethylammonium chloride, and 2-aminoethyl methacrylate hydrochloride. Typical oil-soluble initiators were benzoyl and lauroyl peroxides. In some cases, water-soluble potassium persulfate was used, both separately and in mixtures with oil-soluble peroxides. Of the water-in-oil emulsifiers, one of the most effective was Span 60 (technical sorbitan monostearate. Atlas Chemical Industries, Inc.). [Pg.35]

Water is the solvent of choice for ionic monomers such as sodium methacrylate, where a direct radical polymerization (i.e., with the nonprotected form of the monomer) is carried out with the copper-based systems in aqueous media (pH 8—9) at 90 °C to afford controlled molecular weights and narrow MWDs.200 Another ionic monomer, sodium 4-vinylbenzoate, is polymerized very fast in aqueous media (pH 11) at 20 °C.247 An ammonium salt monomer, [2-(methacryl-oxy)ethyl]trimethylammonium chloride (FM-6 Figure 12), was polymerized in water with CuBr/L-1 in conjunction with a surface-confined initiator, while... [Pg.478]

Typically, carboxylate ionomers are prepared by direct copolymerization of acrylic or methacrylic acid with ethylene, styrene or similar comonomers by free radical copolymerization (65). More recently, a number of copolymerizations involving sulfonated monomers have been described. For example, Weiss et al. (66-69) prepared ionomers by a free-radical, emulsion copolymerization of sodium sulfonated styrene with butadiene or styrene. Similarly, Allen et al. (70) copolymerized n-butyl acrylate with salts of sulfonated styrene. The ionomers prepared by this route, however, were reported to be "blocky" with regard to the incorporation of the sulfonated styrene monomer. Salamone et al. (71-76) prepared ionomers based on the copolymerization of a neutral monomer, such as styrene, methyl methacrylate, or n-butyl acrylate, with a cationic-anionic monomer pair, 3-methacrylamidopropyl-trimethylammonium 2-acrylamlde-2-methylpropane sulfonate. [Pg.20]

Moschou et al. used the compact disc microfluidic platform that is spun to allow the centripetal force to achieve pumping of the mobile phase through the channel. They incorporated a poly(2-hydroxyethyl methacrylate-co-ethylene dimethacrylate-co-[2-(methacryloyloxy) ethyl] trimethylammonium chloride) monolith in the channel of a poly(dimethylsiloxane) (PDMS) chip. The unusual feature of this preparation is the use of irradiation with microwaves in a common domestic microwave oven to initiate the polymerization reaction, which is then completed in only 4.5 min. This is a significantly shorter time compared to 20 h required to obtain monolith using thermally initiated polymerization of the same mixture. This monolith was then used for the purification of enhanced green fluorescent protein in ion-exchange mode. [Pg.1301]

Chem. Descrip. 2-Trimethylammonium ethyl methacrylate chloride with 600 60 ppm MEHQ inhibitor (75% sol n. in water)... [Pg.522]

PEAA-co-XMA (X = butyl or hexyl). The cationic block, based on trimethylammonium ethyl methacrylate, was also modified with hydrophobic groups. These polymers showed the ability to silence GAPDH expression upon the deUvery of anti-GAPDH siRNA in the MCF-7 cell line. [Pg.301]

Figure 16 Outline of the cleavage and characterization of side chains in molecular brushes (a) P/iBA side chains by acid solvolysis, and (b) poly [2-(trimethylsilyloxy)ethyl methacrylate] (PTMS-HEMA) side chains or poly[[2-(methacryloyloxy)ethyl] trimethylammonium iodide] (PMETAI) side chains by basic hydrolysis. Figure 16 Outline of the cleavage and characterization of side chains in molecular brushes (a) P/iBA side chains by acid solvolysis, and (b) poly [2-(trimethylsilyloxy)ethyl methacrylate] (PTMS-HEMA) side chains or poly[[2-(methacryloyloxy)ethyl] trimethylammonium iodide] (PMETAI) side chains by basic hydrolysis.
The cationic polymer is selected from salts of poly(vinyl amine) or copolymers from 2-(acryloyloxy)ethyl-trimethylammonium chloride and 3-(trimethoxysilyl)propyl methacrylate (3). [Pg.273]


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See also in sourсe #XX -- [ Pg.138 ]




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Trimethylammonium

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