Propylene glycol/maleic

Propylene glycol Maleic anhydride Phthalic anhydride... 

Next, the obtained polyesters and copolyesters were dissolved in styrene or vinyl acetate forming lyotropic liquid-crystalhne thermoset (LLCT) systems, capable of thermal crosslinking by the addition of a free-radical initiator. The thermal and hquid crystal properties of the novel UPs were investigated. It was also reported that UPRs prepared from propylene glycol, maleic anhydride and isophthaUc acid were used as a matrix for nematic liquid-crystal droplets [23]. 

Used as fibres, particularly in textiles and film. Many other polyester polymers are of importance, e.g. unsaturated polyester resins from phthalic anhydride, propylene glycol and maleic anhydride used with reinforcement in boats, cars, etc. (alkyd resins). U.S. production 1983 1-7 megatonnes. 

Uses. About 35% of the isophthahc acid is used to prepare unsaturated polyester resins. These are condensation products of isophthahc acid, an unsaturated dibasic acid, most likely maleic anhydride, and a glycol such as propylene glycol. The polymer is dissolved in an inhibited vinyl monomer, usually styrene with a quinone inhibitor. When this viscous hquid is treated with a catalyst, heat or free-radical initiation causes cross-linking and sohdification. A range of properties is possible depending on the reactants used and their ratios (97). 

The properties of polymers formed by the step growth esterification (1) of glycols and dibasic acids can be manipulated widely by the choice of coreactant raw materials (Table 1) (2). The reactivity fundamental to the majority of commercial resins is derived from maleic anhydride [108-31-6] (MAN) as the unsaturated component in the polymer, and styrene as the coreactant monomer. Propylene glycol [57-55-6] (PG) is the principal glycol used in most compositions, and (i9f2v (9)-phthahc anhydride (PA) is the principal dibasic acid incorporated to moderate the reactivity and performance of the final resins. 

The cleavage of dicyclopentadiene into cyclopentadiene can be accomplished at temperatures above 160°C, producing the heterocycHc Diels-Alder maleic addition product, which opens to the diacid. This product can be esterified with propylene glycol to produce resins that demonstrate enhanced resihence and thermooxidative resistance suitable for molded electrical components. 

The basic patent (US Patent 3256219) indicates that the system is viable with conventional resins although special grades have been developed that are said to be particularly suitable. One example in the patent recommends the use of a polyester prepared using a maleic acid, phthalic acid and propylene glycol ratio of 2 1 33 and with an acid value of 40. To 500g of such a resin are added 10g of benzoyl peroxide and 167 g of styrene. Water 600 g is then stirred in at 5-10°C until a white creamy water-in-oil emulsion is obtained. A solution of 0.8 g of dimethyl-p-toluidine in lOOg of styrene is stirred into the emulsion and the resin is cast between plates and cured at 50°C. 

About 60% of the propylene oxide made is polymerized to polypropylene glycol and other polyethers for use in polyurethane foams and adhesives. Propylene glycol is also widely used in polyester resins based on maleic anhydride. 

As is often said, the simplest unsaturated polyester resin (UPR) is the condensation product of maleic anhydride and propylene glycol dissolved in styrene. 

A 41 resin reactor, equipped with a condensor, a stirrer and a nitrogen inlet, is charged with a polyether polyol and maleic anhydride. The mixture is heated to 60 °C and the catalyst is added. The mixture is then heated to 185 °C for 10 h or until the acid number is reduced to 140mgKOH/g. Some propylene glycol is added and the mixture is maintained at this temperature for another 4h or until the acid number is lowered to about 40mgKOH/g. The yield is about 90 %. 

An unsaturated polyester resin consists of a linear polyester whose chain contains double bonds and an unsaturated monomer such as styrene that copolymerizes with the polyester to provide a cross-linked product. The most common unsaturated polyester is made by step growth polymerization of propylene glycol with phthalic and maleic anhydrides. Subsequent treatment with styrene and a peroxide catalyst leads to a solid, infusible thermoset. 

Maleic and phthalic anhydrides with propylene glycol Cross-linked with free radical initiator and styrene... 

Thermoset polymeric esters consisting of neopentyl glycol, propylene glycol, trimethylol propane, adipic acid, maleic anhydride, and 2-ethyl hexanol were prepared by McAlvin et al. (3) and were used in blends containing styrene monomer. The mixture was cured by pultrusion and had improved weatherabil-ity characteristics. 

In the manufacture of unsaturated polyester resins the polyester is synthesized and then diluted with a vinyl reactive monomer such as styrene (see POLYESTERS, UNSATURATED). A portion of the dibasic acid of the polyester is maleic or some other vinyl reactive diacid that can be polymerized with the styrene to yield a highly cross-linked, high performance polymer system. Other esters made with propylene glycol, dipropylene glycol, and tripropylene glycol are used as emulsifiers in foods, as plasticizers in polymer systems, and as part of acrylate resin systems. 

The distribution of styrene crosslinks in cured unsaturated polyesters based on maleic anhydride, phthalic anhydride, propylene glycol and dipropylene glycol is found to be dependent on the molar ratio of styrene vs. maleic/fumaric unit. If the molar ratio is higher than 1, the dyad distribution is predominant lower molar ratios yield mostly styrene microdomains, i.e. n-ads with more than 2 styrene repeating units 232>. 

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