Elastic polyurethanes crosslink density

For imperfect epoxy-amine or polyoxypropylene-urethane networks (Mc=103-10 ), the front factor, A, in the rubber elasticity theories was always higher than the phantom value which may be due to a contribution by trapped entanglements. The crosslinking density of the networks was controlled by excess amine or hydroxyl groups, respectively, or by addition of monoepoxide. The reduced equilibrium moduli (equal to the concentration of elastically active network chains) of epoxy networks were the same in dry and swollen states and fitted equally well the theory with chemical contribution and A 1 or the phantom network value of A and a trapped entanglement contribution due to the similar shape of both contributions. For polyurethane networks from polyoxypro-pylene triol (M=2700), A 2 if only the chemical contribution was considered which could be explained by a trapped entanglement contribution. 

Atomic force microscopy and attenuated total reflection infrared spectroscopy were used to study the changes occurring in the micromorphology of a single strut of flexible polyurethane foam. A mathematical model of the deformation and orientation in the rubbery phase, but which takes account of the harder domains, is presented which may be successfully used to predict the shapes of the stress-strain curves for solid polyurethane elastomers with different hard phase contents. It may also be used for low density polyethylene at different temperatures. Yield and rubber crosslink density are given as explanations of departure from ideal elastic behaviour. 17 refs. 

Creep behavior of a single sample at three different crosslink densities is depicted in Figure 4, vq being the virgin network sample which was crossllnked by irradiating for 30 minutes to yield which was further Irradiated 30 minutes to yield V2. In the previous work on polyurethane samples, values obtained from equation 3 were used to determine the rubber elasticity vertical... 

Telechelic polymers rank among the oldest designed precursors. The position of reactive groups at the ends of a sequence of repeating units makes it possible to incorporate various chemical structures into the network (polyether, polyester, polyamide, aliphatic, cycloaliphatic or aromatic hydrocarbon, etc.). The cross-linking density can be controlled by the length of precursor chain and functionality of the crosslinker, by molar ratio of functional groups, or by addition of a monofunctional component. Formation of elastically inactive loops is usually weak. Typical polyurethane systems composed of a macromolecular triol and a diisocyanate are statistically simple and when different theories listed above are... 

The cured silane crosslinking spray foams exhibit very good mechanical properties. They possess a high hardness and a very good elasticity. The compressive strength is comparable to common polyurethane (PU) spray foams. Foam densities < 40 kg/m, i.e. the densities of common PU foams,... 

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