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Methacrylic acid-ethylene glycol copolymers

Another example of new sorbents is the molecular imprinted polymers (MIP) from the work of Siemann and co-workers (1996). They synthesized a methacrylic acid-ethylene glycol dimethacrylate copolymer with atrazine as an imprint molecule. Imprint synthesis entails polymerization around an imprint species with monomers that are selected for their ability to form specific and definable interactions with the imprint molecule. The atrazine is chemically removed from the polymer leaving holes or cavities. The cavities are formed in the polymer matrix whose size and shape are complementary to that of the imprint molecule (Siemann et al., 1996). These recognition sites enable the polymer to rebind the imprint species selectively from a mixture of closely related compounds, in many instances with binding affinities approaching those demonstrated by antigen-antibody systems. [Pg.321]

Acrylic acid-methyl methacrylate copolymer esterified to an unknown degree to methyl acrylate Acrylic acid-styrene copolymer esterified to an unknown degree to methyl acrylate Ethylene-methacrylic acid copolymer neutralized to an unknown degree to sodium methacrylate Isophthalic acid-ethylene glycol copolymer post-treated to form the diallyl ester 2-Propenoic acid, 2-methyl-, methyl ester, polymer with 2-propenoic acid, methyl ester 2-Propenoic acid, poljrmer with ethenylbenzene, methyl ester 2-Propenoic acid, 2-methyl-, polymer with ethene, sodium salt 1,3-Benzenedicarboxylic acid, polymer with 1,2-ethanediol, di-2-propenyl ester... [Pg.5062]

A review is presented on the controlled release of calcitonins from polymeric matrices and oil-based formulations covering the period 1992-8. Polymers covered include biodegradable polymers, such as polyglycolic acid, polylactic acid and copolymers thereof, and non-biodegradable polymers, such as styrene-isopropyl acrylamide copolymers and poly(methacrylic acid-g-ethylene glycol) copolymers, for oral calcitonin delivery systems. 28 refs. [Pg.93]

An adipic acid-diethylene glycol copolymer, by treatment with a THF polymer or polypropylene glycol in the presence of chlorosulfonic acid, afforded polyether polyesters useful for the preparation of thermoplastic block copolyester rubbers and polyurethans. Strongly acid sulfonate derivatives of hydrophilic polymers may be prepared by reacting glycidyl methacrylate-ethylene dimethacrylate copolymer or ethylene dimethacrylate-glycidyl methacrylate-styrene copolymer with chlorosulfonic acid or oleum at 0-60 °C. ... [Pg.249]

Acryhc stmctural adhesives have been modified by elastomers in order to obtain a phase-separated, toughened system. A significant contribution in this technology has been made in which acryhc adhesives were modified by the addition of chlorosulfonated polyethylene to obtain a phase-separated stmctural adhesive (11). Such adhesives also contain methyl methacrylate, glacial methacrylic acid, and cross-linkers such as ethylene glycol dimethacrylate [97-90-5]. The polymerization initiation system, which includes cumene hydroperoxide, N,1S7-dimethyl- -toluidine, and saccharin, can be apphed to the adherend surface as a primer, or it can be formulated as the second part of a two-part adhesive. Modification of cyanoacrylates using elastomers has also been attempted copolymers of acrylonitrile, butadiene, and styrene ethylene copolymers with methylacrylate or copolymers of methacrylates with butadiene and styrene have been used. However, because of the extreme reactivity of the monomer, modification of cyanoacrylate adhesives is very difficult and material purity is essential in order to be able to modify the cyanoacrylate without causing premature reaction. [Pg.233]

Several polymer-related uses of brassylic acid (BA) have been investigated. For example, a BA/l,3-butanediol/lauric acid oligomer is an effective plasticizer for poljrvinyl chloride,[6] BA/ethylene glycol and BA/propylene glycol polymers function as polyester based polyurethane elastomers,[7] and BA has been patented as a cross-linker for glycidyl methacrylate copolymer powder coatings.[8] However, the most detailed studies have involved polyamides selected data from these studies are summarized in Table I. [Pg.222]

Becer CR, Hahn S, Fijten MWM, Thijs HML, Hoogenboom R, Schubert US (2008) Libraries of methacrylic acid and oligo(ethylene glycol) methacrylate copolymers with LCST behavior. J Polym Sci Part A Polym Chem 46 7138-7147... [Pg.14]

Byme et al. [124] have shown the possibility of creating imprinted polymer ordered micropattems, of a variety of shapes and dimensions, on polymer and silicon substrates using iniferters and photopolymerization. They applied this approach to the recognition of D-glucose using copolymer networks containing poly(ethylene glycol) and functional monomers such as acrylic acid, 2-hydro-xyethyl methacrylate, and acrylamide. [Pg.157]

Poly( ethylene oxide)-block-poly (propylene oxide)-hZock-poly(ethylene oxide)-g-poly(acrylic acid) (PEO-fc-PPO-fc-PEO-g-PAA, Pluronic-PAA) graft copolymers were synthesized by free radical grafting copolymerization of acrylic acid monomers onto PEO-h-PPO-h-PEO (Pluronic F127) and the aqueous solution properties were characterized by Bromberg [133, 134]. Chiu et al. [135] reported on the micellization of (non-ionic) poly(stearyl methacrylate)-gra/f-poly(ethylene glycol) graft copolymers. [Pg.204]

PVC can be blended with numerous other polymers to give it better processability and impact resistance. For the manufacture of food contact materials the following polymerizates and/or polymer mixtures from polymers manufactured from the above mentioned starting materials can be used Chlorinated polyolefins blends of styrene and graft copolymers and mixtures of polystyrene with polymerisate blends butadiene-acrylonitrile-copolymer blends (hard rubber) blends of ethylene and propylene, butylene, vinyl ester, and unsaturated aliphatic acids as well as salts and esters plasticizerfrec blends of methacrylic acid esters and acrylic acid esters with monofunctional saturated alcohols (Ci-C18) as well as blends of the esters of methacrylic acid butadiene and styrene as well as polymer blends of acrylic acid butyl ester and vinylpyrrolidone polyurethane manufactured from 1,6-hexamethylene diisocyanate, 1.4-butandiol and aliphatic polyesters from adipic acid and glycols. [Pg.31]


See other pages where Methacrylic acid-ethylene glycol copolymers is mentioned: [Pg.26]    [Pg.1520]    [Pg.71]    [Pg.143]    [Pg.3758]    [Pg.619]    [Pg.251]    [Pg.748]    [Pg.491]    [Pg.51]    [Pg.195]    [Pg.82]    [Pg.96]    [Pg.22]    [Pg.533]    [Pg.25]    [Pg.13]    [Pg.91]    [Pg.5]    [Pg.156]    [Pg.909]    [Pg.9]    [Pg.192]    [Pg.69]    [Pg.127]    [Pg.136]    [Pg.233]    [Pg.289]    [Pg.5]    [Pg.11]    [Pg.14]    [Pg.365]    [Pg.368]    [Pg.1738]    [Pg.2452]    [Pg.2533]    [Pg.46]    [Pg.368]    [Pg.38]   
See also in sourсe #XX -- [ Pg.32 ]




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Acid copolymers

Acids methacrylic acid

Copolymer methacrylate

Copolymers acidic

Copolymers ethylene

Copolymers methacrylic

Ethylene acidity

Ethylene acids

Ethylene glycol acidity

Ethylene methacrylate

Ethylene-acid copolymers

Ethylene-methacrylic acid copolymers

Glycol methacrylate

Glycolic acid / Glycolate

Glycolic acid Glycols

Glycolic acid copolymers

Glycollic acid

METHACRYLIC ACID COPOLYMER

Methacrylic acid

Methacrylic acid methacrylate

Methacrylic acid-ethylene glycol

Methacrylic ethylene

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