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Polymers hydroxyl-terminated, curing

The diisocyanates and polyols are reacted to form a high molecular weight hydroxyl terminated millable gum. These millable gums are compounded and processed as conventional elastomers, both sulphur and peroxides being used to cure the polymers. Here again, polyether and polyester types are available, and the differences between these two types referred to above also apply here. [Pg.111]

The effect of curing on the diffusion of polymer and the curing agent is studied for the system of hydroxyl-terminated polybutadiene (R-45-M)/isophorone disso-cyanate (IPDI). Both components contribute to the echo intensity and the plot of In P(x)/I(0)] vs (G5)2 (A — 5/3) consists of two exponentials (Eq. (22)) the fast component (the steep intial slope) is attributed to the IPDI, and the long component to the R-45-M. The dependence of both diffusion constants on the curing time is shown in Fig. 19. The accuracy for Dfast data is less pronounced than for the polymer D(Mn), because only the first few data points are relevant for its determination. Furthermore, the low tail of the R-45-M molecular weight distribution nearly coin-... [Pg.40]

Summary Two-component room temperature-vulcanizing, condensation-curing systems (RTV-2) are well known in silicone chemistry. Even silicone-based materials caimot fulfill all requirements in diverse applications. It is therefore desirable to combine the curing properties of silicone-based systems with those of other polymer backbones. The use of isocyanatomethyl-dimethylmonomethoxysilane allows the straightforward derivatization of, e.g., hydroxyl-terminated polymers, which yield mono-silanol-terminated polymers upon hydrolysis. [Pg.765]

Two-Package Polyol Urethane Coatings (ASTM Type 5). Two-package polyol urethane coatings consist of isocyanate-terminated adducts of polymers that are cured by reaction with di- or polyfunctional hydroxyl-containing materials. The latter may consist of low- to medium-weight polyols with a polyester, polyether, polyether urethane, or castor oil backbone. When the two components (OH- and NC0-) are mixed together, they have only a limited pot life. Therefore, the components are mixed prior to application. Catalysts may be used to speed up the cure either for room temperature or oven cure. [Pg.1008]

The dimethylsiloxane polymers in condensation-curing systems have hydroxyl functions as terminal reactive groups. [Pg.712]

There are many different formulations for two component polyurethane sealants dependent of the sealant properties required. The usual NCO/OH equivalent ratio is 1.05 to 1.10. One component is a liquid isocyanate-terminated prepolymer containing pigments, fillers such as calcimn carbonate or talc, and an antisag agent such as fimied silica. The second component is a hydroxyl terminated polymer, pigment, and a catalyst such as methylene dianiline. The individual components are mixed at elevated temperatures under dry conditions so that premature crosslinking does not occur. Prior to use, the two components are mixed well and have a pot life of about 1 to 4 hours. Cure time to develop full sealant properties is 1 to 2 days. [Pg.323]

Two types of solid product are prepared commercially, viz hydroxyl-and thiol-terminated polymers. The significance of the nature of the end-groups lies in the means whereby the polymer may be cured (see section 19.5). [Pg.440]


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Hydroxyl termination

Hydroxylated polymers

Polymer curing

Polymers hydroxyl terminated

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