Thermoset Polymer Materials

A number of plastic, adhesive, and coating materials are utilized in a densely cross-linked form known as thermosets. Some of the more important of these include the phenol-formaldehyde resins, urea-formaldehydes, polyimides, epoxies, amino resins, and the alkyds, among others (8). Because these 

These materials are produced by heating phenol and formaldehyde in the presence of either an acid or a base catalyst. With a base catalyst and an excess of formaldehyde, a composition called resole resins are prepared. With an acid catalyst and an excess of phenol, a two-stage resin called novolacs are made. In both cases high-melting or viscous oligomers are made, which react further at elevated temperatures to produce high modulus but brittle materials (9). 

The basic structure of these materials in the fully cured (cross-linked) state may be written 

The open bonds indicate points of attachment to other regions of the network. Of course, this structure is only an illustration of the very many possibilities of a very irregular network. Applications include electrical connectors, pot handles, and so on. 

One of the most important monomers in epoxy chemistry is the diglycidyl ether of bisphenol A (9a)  

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Another way to classify polymers results from the consideration of their typical applications. Typical classes are Compression molding compounds, injection molding compounds, semi-finished products, films, fibers, foams (urethane foam, styrofoam), adhesives (synthetic adhesives are based on elastomers, thermoplastics, emulsions, and thermosets. Examples of thermosetting adhesives are Epoxy, polyurethane, cyanoacrylate, acrylic polymers), coatings, membranes, ion exchangers, resins (polyester resin, epoxy resin, vinylether resin), thermosets (polymer material that irreversibly cures), elastomers (BR, silicon rubber). 

B73.5M-1995 Thermoplastic and Thermoset Polymer Material Horizontal End Suc on Centrifugal Pumps for Chemical Process... 

In this section we examine some examples of cross-linked step-growth polymers. The systems we shall describe are thermosetting polymers of considerable industrial importance. The chemistry of these polymerization reactions is more complex than the hypothetical AB reactions of our models. We choose to describe these commercial polymers rather than model systems which might conform better to the theoretical developments of the last section both because of the importance of these materials and because the theoretical concepts provide a framework for understanding more complex systems, even if they are not quantitatively successful. 

Polymers are characteri2ed as thermosetting and thermoplastic with respect to the methods by which they are joined. Thermosetting polymers are permanently hard and do not soften upon the apphcation of heat they are joined by mechanical fasteners and adhesives. Several methods have been devised to join thermoplastic polymers, as weU as thermoplastic composite materials, which soften upon heating. 

Thermosetting Reactive Polymers. Materials used as thermosetting polymers include reactive monomers such as urea—formaldehyde, phenoHcs, polyesters, epoxides, and vinyls, which form a polymerized material when mixed with a catalyst. The treated waste forms a sponge-like material which traps the soHd particles, but not the Hquid fraction the waste must usually be dried and placed in containers for disposal. Because the urea—formaldehyde catalysts are strongly acidic, urea-based materials are generally not suitable for metals that can leach in the untrapped Hquid fractions. Thermosetting processes have greater utiHty for radioactive materials and acid wastes. 

Synthetic Resins. Various polymers and resins are utilized to produce some specialty carbon products such as glassy carbon or carbon foam and as treatments for carbon products. Typical resins include phenoHcs, furan-based polymers, and polyurethanes. These materials give good yields of carbon on pyrolysis and generally carbonize directly from the thermoset polymer state. Because they form Httle or no mesophase, the ultimate carbon end product is nongraphitizing. 

Polyurethanes are thermoset polymers formed from di-isocyanates and poly functional compounds containing numerous hydroxy-groups. Typically the starting materials are themselves polymeric, but comprise relatively few monomer units in the molecule. Low relative molar mass species of this kind are known generally as oligomers. Typical oligomers for the preparation of polyurethanes are polyesters and poly ethers. These are usually prepared to include a small proportion of monomeric trifunctional hydroxy compounds, such as trimethylolpropane, in the backbone, so that they contain pendant hydroxyls which act as the sites of crosslinking. A number of different diisocyanates are used commercially typical examples are shown in Table 1.2. 

Composites consist of two (or more) distinct constituents or phases, which when combined result in a material with entirely different properties from those of the individual components. Typically, a manmade composite would consist of a reinforcement phase of stiff, strong material, embedded in a continuous matrix phase. This reinforcing phase is generally termed as filler. The matrix holds the fillers together, transfers applied loads to those fillers and protects them from mechanical damage and other environmental factors. The matrix in most common traditional composites comprises either of a thermoplastic or thermoset polymer [1]. 

Details are given of the development of energy and material recycling processes for thermosetting polymer composites. Applications in the cement industry and in coal fired fluidised bed combustion plants are discussed. 3 refs. 

Epoxy resins are widely used in high-strength adhesives, corrosion-resistant coatings, and corrosion-resistant pipes and tanks. The simplest starting material for these thermoset polymers is made from phenol, acetone (to bisphenol A), and epichlorohydrin. 

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