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Polyester resin reactivity

As in polyester resins, reactive halogens containing fire-retardant chemicals are most often used in epoxy materials. Tetrabromobisphenol A is perhaps the most widely used component for flame-retarding epoxy resins. Nara and Matsuyama (24) and Nara et al. (25) described the thermal degradation and flame retardance of tetrabrominated bisphenol A diglycidyl ether compared to the nonbrorainated structure. Their results indicate that bromine acts by vapor-phase as well as condensed-phase mechanisms of flame inhibition. [Pg.317]

Polyester resins can also be rapidly formed by the reaction of propylene oxide (5) with phthaUc and maleic anhydride. The reaction is initiated with a small fraction of glycol initiator containing a basic catalyst such as lithium carbonate. Molecular weight development is controlled by the concentration of initiator, and the highly exothermic reaction proceeds without the evolution of any condensate water. Although this technique provides many process benefits, the low extent of maleate isomerization achieved during the rapid formation of the polymer limits the reactivity and ultimate performance of these resins. [Pg.314]

Dicylopentadiene Resins. Dicyclopentadiene (DCPD) can be used as a reactive component in polyester resins in two distinct reactions with maleic anhydride (7). The addition reaction of maleic anhydride in the presence of an equivalent of water produces a dicyclopentadiene acid maleate that can condense with ethylene or diethylene glycol to form low molecular weight, highly reactive resins. These resins, introduced commercially in 1980, have largely displaced OfXv o-phthahc resins in marine apphcations because of beneficial shrinkage properties that reduce surface profile. The inherent low viscosity of these polymers also allows for the use of high levels of fillers, such as alumina tfihydrate, to extend the resin-enhancing, fiame-retardant properties for apphcation in bathtub products (Table 4). [Pg.316]

Reactive (unsaturated) epoxy resins (qv) are reaction products of multiple glycidyl ethers of phenoHc base polymer substrates with methacrylic, acryhc, or fumaric acids. Reactive (unsaturated) polyester resins are reaction products of glycols and diacids (aromatic, aUphatic, unsaturated) esterified with acryhc or methacrylic acids (see POLYESTERS,unsaturated). Reactive polyether resins are typically poly(ethylene glycol (600) dimethacrylate) or poly(ethylene glycol (400) diacrylate) (see PoLYETPiERs). [Pg.428]

OC-Methylstyrene. This compound is not a styrenic monomer in the strict sense. The methyl substitution on the side chain, rather than the aromatic ring, moderates its reactivity in polymerization. It is used as a specialty monomer in ABS resins, coatings, polyester resins, and hot-melt adhesives. As a copolymer in ABS and polystyrene, it increases the heat-distortion resistance of the product. In coatings and resins, it moderates reaction rates and improves clarity. Physical properties of a-methylstyrene [98-83-9] are shown in Table 12. [Pg.490]

Polyester Resins. Reinforced polyester resins are thermosets based on unsaturated polyesters from glycols and dibasic acids, either or both of which contain reactive double bonds. The ratio of saturated to unsaturated components controls the degree of cross-linking and thus the rigidity of the product (see Polyesters, unsaturated). Typically, the glycols and acids are esterified until a viscous Hquid results, to which an inhibitor is added to prevent premature gelation. Addition of the monomer, usually styrene, reduces the viscosity to an easily workable level. [Pg.328]

Because of the unusual reactivity of the DCPD molecule, there are a number of wide and varying end use areas. The primary uses in the U.S. are DCPD-based unsaturated polyester resins (36%) hydrocarbon type resins, based on DCPD alone or with other reactive olefins (39%) EPDM elastomers via a third monomer ethylidenenorhornene or DCPD (16%) and miscellaneous uses (9%), including polychlorinated pesticides, polyhalogenated flame retardants, and polydicyclopentadiene for reaction injection mol ding (39). [Pg.434]

Many other acids, glycols and reactive monomers have been described in the literature but these remain of either minor or academic importance. In a number of cases this is simply because of the high cost of the chemical and a reduction in cost due to its widespread use in some other application could well lead to extensive use in polyester resins. [Pg.701]

Besides resin and reactive diluent, additives are commonly incorporated into polyester resins. These include not only curing agents and fillers (see Section 25.2.3) but also ultraviolet stabilisers. The latter are particularly important for outdoor applications such as roof lighting, benzotriazoles being particularly effective. [Pg.701]

Self-leveling epoxy, polyester or reactive acrylic resin systems 9/105... [Pg.99]

Saturable dye absorber, 14 677 Saturated aqueous salt solution, 9 34 Saturated calomel electrode (SCE), 9 571 Saturated fatty acids, 10 829, 830 Saturated hydrocarbons adsorbent affinity, 1 674 adsorption by zeolites, 1 624 fluorine reactivity with, 11 831 isomerization of, 12 172—173 Saturated polyester resins, based on trimethylpentanediol, 12 673 Saturated polyesters, 10 7 Saturated synthetic rubber, 10 705 Saturation and coating processes, 10 12-13 Saturation bonding, 17 509-510 Saturation color, 19 262 Saturation concentration, 15 677 Saturation index... [Pg.820]

Unsaturated polyester resin (UPR) has two main components, i.e. a polyester and a reactive diluent. [Pg.700]

Figures 10 and 11 show the weight change and the retention of strength for iso-phthalic unsaturated polyester resin (iso-UP). These behaviors show almost the same tendency as MTHPA-EP, however, as shown in Figure 12 the concentration influences flexural strength and the strength becomes minimum at the concentration of 30wt%. This behavior is thought to depend on contradictory tendency of the wetability and the reactivity with the concentration. Figures 10 and 11 show the weight change and the retention of strength for iso-phthalic unsaturated polyester resin (iso-UP). These behaviors show almost the same tendency as MTHPA-EP, however, as shown in Figure 12 the concentration influences flexural strength and the strength becomes minimum at the concentration of 30wt%. This behavior is thought to depend on contradictory tendency of the wetability and the reactivity with the concentration.
Uses. Reactive free radical-generating chemical used as a curing agent for unsaturated polyester resins hardening agent for fiberglass-reinforced plastics manufacture of acrylic... [Pg.478]

Although polyurethanes or other reactive resins can be used in RTM, the most common resins are polyesters and epoxies. The two pumping reservoirs in Figure 7.90, then, contain polyester resin and initiator, or epoxy resin and hardener, respectively. Epoxies require relatively long cycle times. When cycle time is critical, low viscosity vinyl ester, acrylamate, or urethanes can be injected very rapidly into the mold. Even the use of thermoplastics is possible. [Pg.799]

Bis(bromomethyl)propane-l,3-diol is a reactive flame retardant that is used primarily in unsaturated polyester resins for moulded products and in rigid polyurethane... [Pg.456]

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. [Pg.366]

Of particular importance in describing the difference between these two families of resins are the locations of die reactive unsaturation. In the polyester resin, these groups are located along the backbone of die polymer with terminal hydroxyl or carboxylic acid groups. The vinyl ester resins contain no significant acidity but terminate in reactive vinyl ester groups. Because of the location of these reactive sites, the vinyl ester resins will homopolymerize as well as coreact with various vinyl monomers. [Pg.1688]


See other pages where Polyester resin reactivity is mentioned: [Pg.4473]    [Pg.4473]    [Pg.361]    [Pg.366]    [Pg.368]    [Pg.372]    [Pg.222]    [Pg.225]    [Pg.316]    [Pg.321]    [Pg.162]    [Pg.337]    [Pg.696]    [Pg.106]    [Pg.59]    [Pg.41]    [Pg.789]    [Pg.504]    [Pg.523]    [Pg.175]    [Pg.185]    [Pg.361]    [Pg.368]    [Pg.372]    [Pg.316]    [Pg.321]    [Pg.1556]    [Pg.1688]    [Pg.106]   
See also in sourсe #XX -- [ Pg.216 ]




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