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Thermosetting scheme

The final general approach can be considered a thermosetting scheme [12] (Fig. 20). With this method, lattice hardening occurs during both spin casting and poling... [Pg.637]

The thermoset included here is derived from bisphenol-A dicya-nate. It can be thermally trimerized yielding a triazine or cyanurate network (8,9,10) as seen in the reaction scheme (Table 1). The critical molecular weight between crosslinks is relatively low, resulting in an extremely tight, brittle network. The material is usually used as a prepeg because a total cure produces a hard, infusible, and insoluble matrix. It possesses excellent adhesive properties and is currently used as a metal coupling agent. It offers many superior properties relative to conventional epoxies derived from bisphenol-A. [Pg.246]

After three decades of accumulating experimental results, we should be expected to have an almost complete knowledge of the rate equations that describe the most important thermosetting polymerizations. Unfortunately, the situation seems to be quite different on the one hand, some authors persist in using intrinsically incorrect methodologies to analyze kinetic data on the other hand, even for the most studied systems - e.g., the epoxy-amine reaction - no general kinetic schemes are universally accepted. [Pg.157]

SCHEME 2.5 Initial chain scissions in polyester.53 (From Levchik, S.V., Thermosetting polymers, in Plastics Flammability Handbook, Troitzsch, J. (ed.), Hanser, Munich, 2004, pp. 83-98.)... [Pg.26]

Although the major interest in experimental and theoretical studies of network formation has been devoted to elastomer networks, the epoxy resins keep apparently first place among typical thermosets. Almost exclusively, the statistical theory based on the tree-like model has been used. The problem of curing was first attacked by Japanese authors (Yamabe and Fukui, Kakurai and Noguchi, Tanaka and Kakiuchi) who used the combinatorial approach of Flory and Stockmayer. Their work has been reviewed in Chapter IV of May s and Tanaka s monograph Their experimental studies included molecular weights and gel points. However, their conclusions were somewhat invalidated by the fact that the assumed reaction schemes were too simplified or even incorrect. It is to be stressed, however, that Yamabe and Fukui were the first who took into account the initiated mechanism of polymerization of epoxy groups (polyetherification). They used, however, the statistical treatment which is incorrect as was shown in Section 3.3. [Pg.24]

Elimination of side-chains, followed by cross-linking and creating a porous charred residue, including the non-volatile additives. This scheme is followed by most thermosets and other cross-linked polymers. [Pg.13]

Sellinger and Laine [34] presented methacrylate/cube hybrids (XXIX) (Scheme 8) that can act as thermosets or photocurable monomers. [Pg.241]

Fig. 30. A scheme for thermosetting mechanism of silyl-carborane hybrid diethynylbenzene-silylene polymer by diene reaction between theC=C group and Ph-C=C group. Fig. 30. A scheme for thermosetting mechanism of silyl-carborane hybrid diethynylbenzene-silylene polymer by diene reaction between theC=C group and Ph-C=C group.
For engineering purposes, the most useful classification of polymers is based on their thermal (thermomechanical) response. Under this scheme, polymers are classified as thermoplastics or thermosets. As the name suggests, thermoplastic polymers soften and flow under the action of heat and pressure. Upon cooling, the polymer hardens and assumes the shape of the mold (container). Thermoplastics, when compounded with appropriate ingredients, can usually withstand several of these heating and cooling cycles without suffering any structural breakdown. This behavior is similar to that of candle wax. Examples of thermoplastic polymers are polyethylene, polystyrene, and nylon. [Pg.30]

A composite is any combination of two or more resources held together by some type of mastic or matrix. The mastic or matrix can be as simple as physical entanglement of fibers to more complicated systems based on thermosetting or thermoplastic polymers. The scheme shown below gives possible processing pathways that lead to the composite products identified in this report that can come from each fraction of the plant. The entire plant (leaves, stock, pith, roots) can be used directly to produce structural and nonstructural composites... [Pg.433]

Next, we will present applications of the CTH scheme in several real-world composite stractures. They arc fiber reinforced syntactic foam cored sandwich structures, sandwich stractures with a continuous fiber reinforced grid stiffened syntactic foam core, and 3-D woven fabric reinforced polymer composite structures. Of course, the core or the polymer composite is based on the same thermosetting PSMP as discussed above. [Pg.244]


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See also in sourсe #XX -- [ Pg.637 ]




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