Injection reinforced

Composites. The history of phenoHc resin composites goes back to the early development of phenoHc materials, when wood flour, minerals, and colorants were combined with phenoHc resins to produce mol ding compounds. In later appHcations, resin varnishes were developed for kraft paper and textile fabrics to make decorative and industrial laminates. Although phenoHcs have been well characterized in glass-reinforced composites, new developments continue in this area, such as new systems for Hquid-injection molding (LIM) and sheet-molding compounds (SMC). More compHcated composite systems are based on aramid and graphite fibers. 

When surfactant-coated glass fibers are included to improve product flexibility and reduce thermal expansion, these semibatch processes are termed reinforced reaction injection mol ding (RRIM). 

Nittile mbber is much like SBR in its physical properties. It can be compounded for physical strength and abrasion resistance using traditional fillers such as carbon black, siUca, and reinforcing clays. The primary benefit of the polymer is its oil and solvent resistance. At a medium ACN content of 34% the swell in IRM 903 oil at 70°C is typically 25—30%. Nitrile mbber processes on conventional mbber equipment and can be compression, transfer, or injection molded. It can also be extmded easily. 

The furnace process involves injecting low end fraction of cmde oil, eg. Bunker Euel C, into a heated chamber. The temperature, shape of the injectors of the oil, rate of injection, and other factors are controlled to produce black fillers of different particle si2e and stmcture. The particle si2e and stmcture control the reinforcing character of the carbon black. There are 30 common grades of carbon black used in the mbber industry. There are numerous specialty grades produced, and several hundred are used in plastic, conductive appHcations, and other uses. 

The largest segment of the CASE family of polyurethanes are elastomers. Cast polyurethane elastomers reached a new dimension when high pressure impingement mixing led to reaction injection molding (RIM). This technology is used widely in the automotive industry, and reinforced versions (RRIM) and stmctural molded parts (SRIM) have been added in more recent years. 

Polypropylene can be fabricated by almost any process used for plastics (see Plastics processing). The extmsion of pipe and injection mol ding of fittings present no unusual problem. However, there is no way to bond the fittings to the pipe except by remelting the polymer, which is impractical on most constmction sites. The resin can be reinforced by glass fibers, mineral fillers, or other types of fillers and can be pigmented readily. 

The resins have wide appHcation. In nonreinforced form they serve as insulating coatings for electrical coils (46—47). As fiber reinforced resins, they can be made by reaction injection mol ding into laminates, castings, and coatings (48—49). Fiber-reinforced resins are used in marine appHcations (recreational boats) automotive parts (50) bathroom countertops and shower stalls and tubs and more recendy as baUistic protection for military vehicles and aircraft. 

Fast concentration and sample injection are considered with the use of a theory of vibrational relaxation. A possibility to reduce a detection limit for trinitrotoluene to 10 g/cnf in less than 1 min is shown. Such a detection limit can by obtained using selective ionization combined with ion drift spectrometry. The time of detection in this case is 1- 3 s. A detection technique based on fluorescent reinforcing polymers, when the target molecules strongly quench fluorescence, holds much promise for developing fast detectors. 

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