Cured polyesters processes

OTHER EXAMPLES OF CURED POLYESTER PROCESSES 2.4.1 System 1... 

Phenanthroline and some of its alkyl-substituted derivatives improve the heat stability of polyesters and magnetic recording tape. They also improve the color of cured polyester resins. They are also useful in various electroplating and electrolytic processes " ... 

Curing polyester resins involves the transformation of the polyester from a liquid to a solid state, taking place on the addition of a catalyst, usually organic peroxide (Table 13.2). To speed up the process, the catalyst has to be activated, either by heating or, by the addition of an accelerator. The crosslinking reaction is exothermic and, since polyester resins are... 

Polyurethane foams used as a core in sandwich structures are usually made by the foam-in-place process. In this process, the skins (cured polyester, epoxy fiberglass, or aluminum) are laid up in a mold, and the urethane foamant is injected into the space between the skins. 

UPRs based on a mixture of maleic anhydride, phthalic anhydride and adipic acid in a molar ration of 1 2 2 were prepared in the presence of the polyesterification catalysts, i.e. lead dioxide, p-toluenesulfonic acid monohydrate and zinc acetate dihydrate, and next crossHnked with styrene by using MEKP as the initiator and cobalt naphthenate (CoNp) as the promoter [197]. Most often, the catalysts used in the polyesterification process cannot be easily separated from the polyester, thus the effect of the residual catalysts on the curing process and color of the cured polyester resin should be taken into account. It was shown that the residual catalyst could affect the curing reaction even in a small amount (Table 28), increasing the activation energy a, frequency factor ko and the reaction order x. 

THPC—Amide—PoIy(vinyI bromide) Finish. A flame retardant based on THPC—amide plus poly(vinyl bromide) [25951-54-6] (143) has been reported suitable for use on 35/65, and perhaps on 50/50, polyester—cotton blends. It is appUed by the pad-dry-cure process, with curing at 150°C for about 3 min. A typical formulation contains 20% THPC, 3% disodium hydrogen phosphate, 6% urea, 3% trimethylolglycouril [496-46-8] and 12% poly(vinyl bromide) soUds. Approximately 20% add-on is required to impart flame retardancy to a 168 g/m 35/65 polyester—cotton fabric. Treated fabrics passed the FF 3-71 test. However, as far as can be determined, poly(vinyl bromide) is no longer commercially available. 

Other common radical-initiated polymer processes include curing of resins, eg, unsaturated polyester—styrene blends curing of mbber grafting of vinyl monomers onto polymer backbones and telomerizations. 

The commonly used resins in the manufacture of decorative and industrial laminates ate thermosetting materials. Thermosets ate polymers that form cross-linked networks during processing. These three-dimensional molecules ate of essentially infinite size. Theoretically, the entire cured piece could be one giant molecule. The types of thermosets commonly used in laminates ate phenoHcs, amino resins (melamines), polyesters, and epoxies. 

The relative effectiveness of nucleating agents in a polymer can be determined by measuring recrystallization exotherms of samples molded at different temperatures (105). The effect of catalyst concentration and filler content has been determined on unsaturated polyesters by using dynamic thermal techniques (124). Effects of formulation change on the heat of mbber vulcanization can be determined by dsc pressurized cells may be needed to reduce volatilization during the cure process (125). 

Catalyst Selection. The low resin viscosity and ambient temperature cure systems developed from peroxides have faciUtated the expansion of polyester resins on a commercial scale, using relatively simple fabrication techniques in open molds at ambient temperatures. The dominant catalyst systems used for ambient fabrication processes are based on metal (redox) promoters used in combination with hydroperoxides and peroxides commonly found in commercial MEKP and related perketones (13). Promoters such as styrene-soluble cobalt octoate undergo controlled reduction—oxidation (redox) reactions with MEKP that generate peroxy free radicals to initiate a controlled cross-linking reaction. 

Vinyl ester resins generally offer mechanical properties superior to those of polyester matrices but at an increased cost. Vinyl esters are chemically similar to epoxy resins but are manufactured via a cold-curing process similar to that used in the manufacture of polyester resins. Vinyl esters offer superior resistance to water and chemical attack and are used in such appHcations as underground pipes, tank liners, and storage tanks (see Vinyl polymers). 

Phenohc resins (qv), once a popular matrix material for composite materials, have in recent years been superseded by polyesters and epoxies. Nevertheless, phenohc resins stiU find considerable use in appHcations where high temperature stabiHty and fire resistance are of paramount importance. Typical examples of the use of phenoHc resins in the marine industry include internal bulkheads, decks, and certain finishings. The curing process involves significant production of water, often resulting in the formation of voids within the volume of the material. Further, the fact that phenoHcs are prone to absorb water in humid or aqueous conditions somewhat limits their widespread appHcation. PhenoHc resins are also used as the adhesive in plywood, and phenohc molding compounds have wide use in household appliances and in the automotive, aerospace, and electrical industries (12). 

Ease of cure, easy removal of parts from mold surfaces, and wide availabiHty have made polyesters the first choice for many fiber-reinforced composite molders. Sheet mol ding compound, filament winding, hand lay-up, spray up, and pultmsion are all weU adapted to the use of polyesters. Choosing the best polyester resin and processing technique is often a challenge. The polyester must be a type that is weU adapted to the processing method and must have the final mechanical properties requked by the part appHcation. Table 1 Hsts the deskable properties for a number of fiber-reinforced composite fabrication methods. 

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