Maleic anhydride/acid copolymer with ethylene

Alkenylsuccinic anhydrides made from several linear alpha olefins are used in paper sizing, detergents, and other uses. Sulfosuccinic acid esters serve as surface active agents. Alkyd resins (qv) are used as surface coatings. Chlorendric anhydride [115-27-5] is used as a flame resistant component (see Flame retardants). Tetrahydrophthalic acid [88-98-2] and hexahydrophthalic anhydride [85-42-7] have specialty resin appHcations. Gas barrier films made by grafting maleic anhydride to polypropylene [25085-53-4] film are used in food packaging (qv). Poly(maleic anhydride) [24937-72-2] is used as a scale preventer and corrosion inhibitor (see Corrosion and corrosion control). Maleic anhydride forms copolymers with ethylene glycol methyl vinyl ethers which are partially esterified for biomedical and pharmaceutical uses (189) (see Pharmaceuticals). 

Examples of acid modified polyolefins are the copolymers of ethylene with acrylic acid or methacrylic acid. Variations include the partially neutralised acid copolymers with metal ions (ionomers) or terpolymers of ethylene, an acid and an acrylate such as methyl acrylate or isobutyl acrylate. Acid-containing extrudable adhesives are widely used to bond to aluminium foil. Examples of anhydride-modified polyolefins include terpolymers of ethylene, maleic anhydride and acrylates such as ethyl acrylate or butyl acrylate and the anhydride-grafted polyolefins. Some typical applications and stmctures of a variety of multilayer materials with extruded polymer tie-layer adhesives, as described in Du-Pont trade literature, are detailed in Table 16.2. 

Copolymers maleic anhydride copolymer with ethylene or vinyl methyl ether, acrylic acid copolymers, and methacrylic acid copolymers (Eudragit)... 

To increase the starch load up to 40-60% in PO a gelatinized starch is used in the films of poly(ethylene-co-acrylic acid) (EAA) or a mixture of EAA/LDPE or LDPE/EMA (ethylene-maleic anhydride). The difficulty with this system is that the high level of filler seriously impairs the mechanical properties, especially in thin films, and the starch is subjected to moisture-absorption problems. LDPE Mn stea-rate/starch showed a decrease of MW during thermo-oxidation and an increase of MW during UV irradiation. In the mixtures, it has been estabhshed that ethylene-acrylic acid copolymer accelerates LDPE oxidative degradation while plasticized starch inhibits it [62]. 

The interaction of the polymer with the filler is promoted by the presence of reactive functionality in the polymer, capable of chemical reaction or hydrogen bonding with the functionality, generally hydroxyl, on the surface of the filler. Thus, carboxyl-containing polymers, e.g. ethylene-acrylic acid copolymers and maleic anhydride- and acrylic acid-grafted polyethylene and polypropylene interact readily with fillers. 

Superabsorbent polymers are now commonly made from the polymerization of acrylic acid blended with sodium hydroxide in the presence of an initiator to form a polyacrylic acid, sodium salt (sometimes referred to as cross-linked sodium polyacrylate). Some of the polymers include polyacrylamide copolymer, ethylene maleic anhydride copolymer, cross-linked carboxy-methyl-cellulose, polyvinyl alcohol copolymers, cross-linked polyethylene oxide, and starch grafted copolymer of polyacrylonitrile to name a few. The latter is one of the oldest SAP forms created. 

In addition, borane-containing POs can be prepared by copolymerization of olefin with borane monomers or by hydroboration of polyolefins including unsaturated groups, such as olefin-divinylbenzene copolymer and olefin-diene copolymers. Many kinds of graft copolymers, such as poly-elhylene-gra/f-poly( vinyl alcohol), PE-g-PMMA, polypropylcnc-gra/f-poly-(maleicanhydride-co-styrene), polypropylene-gra/f-poly(methacrylic acid), polypropylene-gra/f-poly(vinyl alcohol), polypropylene-gra/f-polycaprolac-tone (PP-g-PCL), polypropylcnc-gra/f-poly(methyl methacrylate) (PP-g-PMMA), poly( ethylene-co-propylene)-gra/f-poly(methyl methacrylate) (EPR-g-PMMA), and poly(ethylene-co-propylene)-gra/f-poly(maleic anhydride-costyrene), have been synthesized by such a method resulting in controllable composition and molecular microstructures [63-66]. 

Anhydride Groups. Anhydride groups present on commercially available ethylene-maleic anhydride copolymers are readily reactive with the nucleophile-containing amino acid residues of proteins.11 These groups react directly with lysine residues, for example, to form amide bonds (4.16) ... 

Alkyl phenol ethoxylates can also react with P4O10 yielding alkyl phenol etherphosphates as a mixture of mono-/diesters or with maleic anhydride to yield maleic acid monoesters, which then react with NaHS03 to yield sulphosuccinate monoesters. Alkylphenolpolyglycolether sulphates, phosphates or sulphosuccinates are mainly used as primary anionic emulsifiers for the manufacturing of acrylic, styrene/acrylic or vinyl acetate co-polymer dispersions. Another type of non-ionic emulsifier is block copolymers of ethylene oxide with propylene oxide. 

The same technique can be used to dye a material that is otherwise difficult to dye. An ethylene-propylene copolymer rubber was reacted first with maleic anhydride, then with an aromatic amine dye in an extruder to produce a dyed rubber.81 Dye sites can also be inserted into polyolefins by grafting them with dimethylaminoethyl methacrylate, using azo or peroxide catalysts in an extruder.82 jV-Vinylimidazole has been grafted to polyethylene in an extruder with the help of dicumylperoxide.83 The product was mixed with an acrylic acid-modified polypropylene and used to compatibilize polyethylene and polypropylene. This could be helpful in the recycling of mixed polyolefins from municipal solid waste. Recycling of cross-linked (thermoset) polymers is more of a problem because they cannot be remelted in an extruder. However, they can be if... 

Photosensitized crosslinking of polymers has been the subject of numerous publications [l - 30], concerned mainly with poly(ethylene), poly(vinyl alcohol), various vinyl copolymers, copolymers of maleic anhydride and/or phtalic anhydride with styrene and some polymers derivated from cinnamic acid. The following compounds were used as sensitizers benzophenone, 4-chloro- and 4,4-dimethylbenzophenone [l, 3-6, 8, 9l, oC -and -derivatives of anthraquinone [3, 23] acetophenone, hydroquinone, triphenylmethane and pyridine li.] chlorobenzene and no less than trichlorinated n-paraffins [6], a complex of zink chloride with o-dia-nizidine fill potassium bichromate [l2j, anthracene fl3, 14] 2,5-methoxy-4-amino-trans-stilbene [l5], benzyl ideneacetophenone fl6-l8] -thiophenylacetophenone,... 

Materials. Two samples of polyacrylic acid, PAA-1 (4) and PAA-2, were obtained as gifts from S. C. Johnson Company. Their degrees of polymerization were 3090 and 4420, respectively, as calculated from the intrinsic viscosities of their sodium salts in 0.102V NaBr at 15°C using the appropriate relation of Takahashi and Nagasawa (5). The samples of the hydrolyzed copolymers of maleic anhydride witn ethylene (HEMA) and with methyl vinyl ether (HVMEMA) have been described previously (4). 

Commercially available water soluble copolymers of maleic anhydride with ethylene and methyl vinyl ether (presumably partially hydrolyzed to vicinal carboxylic acids) and triphenylsulfonium triflate were dissolved in water as a casting solvent. Spin-cast films were baked at 130 °C for 10 s, exposed to 254 nm radiation, and postexposure-baked at 130 °C for 40 s. Development with pure water provided negative tone images, presumably due to acid-catalyzed dehydration between vicinal carboxylic acids to form less polar anhydride, as was demonstrated for polarity reversal (4.3.1). However, a copolymer of maleic acid with methyl vinyl ether failed to provide any negative images,... 

The most commonly used compatibilLzers for the blends are graft copolymers of polypropylene with maleic anhydride (PP-g-MAH) (197-203), glycidyl methacrylate (PP-g-GMA) (204,205), and acrylic acid (PP-g-AA) (198,206). They can increase the tensile strength and impact strength of the blends. Favis et al. (207-210) used an ionomer, a copolymer of ethylene and a mixture of methacrylic acid, zinc methacrylate, and isobutylacrylate to compatibUize PP/PA blends and found it effective to decrease the dispersed particles and improve mechanical properties. 

Powder coatings are also formed from ethylene-vinyl acetate copolymers (see Section 3.4). Copolymers of ethylene with maleic acid (anhydride) of low molecular mass are water-soluble, form salts, and undergo cross-linking reactions. 

Among such oxidations, note that liquid-phase oxidations of solid paraffins in the presence of heterogeneous and colloidal forms of manganese are accompanied by a substantial increase (compared with homogeneous catalysis) in acid yield [3]. The effectiveness of n-paraffin oxidations by Co(III) macrocomplexes is high, but the selectivity is low the ratio between fatty acids, esters, ketones and alcohols is 3 3 3 1. Liquid-phase oxidations of paraffins proceed in the presence of Cu(II) and Mn(II) complexes boimd with copolymers of vinyl ether, P-pinene and maleic anhydride (Amberlite IRS-50) [130]. Oxidations of both linear and cyclic olefins have been studied more intensively. Oxidations of linear olefins proceed by a free-radical mechanism the accumulation of epoxides, ROOH, RCHO, ketones and RCOOH in the course of the reaction testifies to the chain character of these reactions. The main requirement for these processes is selectivity non-catalytic oxidation of propylene (at 423 K) results in the formation of more than 20 products. Acrylic acid is obtained by oxidation of propylene (in water at 338 K) in the presence of catalyst by two steps at first to acrolein, then to the acid with a selectivity up to 91%. Oxidation of ethylene by oxygen at 383 K in acetic acid in... 

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