Elastomeric polyethylene

Chlorosulfonated polyethylene Elastomeric alloys Polychloroprene EPDM... 

Polyethylene, elastomeric (very highly branched) Polyethylene, linear low-density Polyethylene, low-density Polyethylene, metallocene linear low-density... 

Polyethylene, elastomeric (yery highly branched) Poly (ethylene imine)... 

Thermoplastics. There are five elastomeric membranes that are thermoplastic. Two materials, chlorinated polyethylene (CPE) and polyisobutylene (PIB), are relatively obscure. Thermoplastic materials can be either heat-fused or solvent-welded. In contrast to Hypalon and uncured EPDM, this abiHty to fuse the membranes together remains throughout the life of the material. However, cleaning of the membrane surface after exposure to weather is required. Correct cleaning procedures for specific membranes are available from the individual manufacturer. 

Waterproof. Waterproofing barrier systems may be either hot- or cold-appHed. The hot-appHed generaUy involve a bituminous material such as asphalt used in conjunction with a reinforcing fabric such as roofing felt, cotton, or glass cloth. Cold-appHed can be bituminous or elastomeric materials either in Hquid or sheet form, with or without fabric reinforcement. Liquid elastomeric treatments include neoprene, polyurethanes, and blends of these or epoxies with bituminous materials. Among the commonly used precured elastomeric sheet materials are neoprene, polyisobutylene, EPDM mbber, and plasticized PVC. Polyethylene and PVC films and nonwoven plastic or glass fabric coated with bituminous materials also find use (78). Because these... 

The properties of elastomeric materials are also greatly iafluenced by the presence of strong interchain, ie, iatermolecular, forces which can result ia the formation of crystalline domains. Thus the elastomeric properties are those of an amorphous material having weak interchain iateractions and hence no crystallisation. At the other extreme of polymer properties are fiber-forming polymers, such as nylon, which when properly oriented lead to the formation of permanent, crystalline fibers. In between these two extremes is a whole range of polymers, from purely amorphous elastomers to partially crystalline plastics, such as polyethylene, polypropylene, polycarbonates, etc. 

Unlike most elastomeric polymers, which are made by direct polymerization of monomers or comonomers, chlorosulfonated polyethylene, as the name implies, is made by chemical modification of a preformed thermoplastic polymer. The chlorination and chlorosulfonation reactions are usually carried out simultaneously but may be carried out ia stages. 

ACS polymers, developed primarily in Japan, are grafts of acrylonitrile and styrene onto elastomeric chlorinated polyethylene. Although the polymer has good weathering properties it is somewhat susceptible to thermal degradation during processing and to date these polymers have been of limited interest. 

Chlorinated polyethylene CPEs provide a very wide range of properties from soft/ elastomeric to hard. They have inherent oxygen and ozone resistance, have improved resistance (compared to PEs) to chemical extraction, resist plasticizers, volatility, and weathering. Products do not fog at high temperatures as do PVCs and can be made flame retardant. 

Chattopadhyay S., Chaki T.K., and Bhowmick A.K., New thermoplastic elastomers from poly(ethyle-neoctene) (engage), poly(ethylene-vinyl acetate) and low-density polyethylene by electron beam technology structural characterization and mechanical properties. Rubber Chem. TechnoL, 74, 815, 2001. Roy Choudhury N. and Dutta N.K., Thermoplastic elastomeric natural rubber-polypropylene blends with reference to interaction between the components. Advances in Polymer Blends and Alloys Technology, Vol. 5 (K. Finlayson, ed.), Technomic Publishers, Pensylvania, 1994, 161. 

Tullock C.W. et al.. Polyethylene and elastomeric polypropylene using alumina-supported bis(arene) titanium, zirconium, and hafnium catalysts, J. Polym. Sci, Part A, Polym. Chem., 27, 3063, 1989. Mueller G. and Rieger R., Propene based thermoplastic elastomers by early and late transition metal catalysis. Prog. Polym. Sci., 27, 815, 2002. 

Choudhury N.R., Chaki T.K., Dutta A., and Bhowmick A.K. Thermal, x-ray and d3mamic mechanical properties of thermoplastic elastomeric natural rubber-polyethylene blends. Polymer, 30, 2047, 1989. Marasch M.J., TPU s Growth from versatility, 53rd Annual Tech. Conference, Antech 95 4088, Boston, May 7-11, 1995. 

Chattopadhyay, S., Chaki, T.K., Bhowmick, A.K., Gao, G.J.P., and Bandyopadhyay, S., Structural characterization of electron-beam crosslinked thermoplastic elastomeric films from blends of polyethylene and ethylene-vinyl acetate copolymers, J. Appl. Polym. Sci., 81, 1936, 2001. 

The data of Table II indicate that the etch rates for CB and its "homologues"—TP, CO (or TO), and EPM—tend to increase monotonically with a decrease in vinylene (-CH=CH-) unsaturation. The elastomeric EPM was chosen instead of crystalline polyethylene as a model for the fully saturated CB to avoid a morphology factor in etch rates, as was observed with crystalline TB. The difference in etch rates for the partially crystalline TO and the elastomeric CO (ratio of about 1.2 1.0) is attributable more to a morphology difference between these polyoctenamers than to the difference in their cis/trans content. Cis/trans content had likewise no perceptible effect on etch rates in the vinyl-containing polybutadienes (see Table I) if there was a small effect, it was certainly masked by the dominant effect of the vinyl groups. 

Polyethylene and polystyrene are examples of plastics subject to environmental stress cracking. Crack resistance tests have shown that surfactants, alcohols, organic acids, vegetable and mineral oils, and ethers provide an active environment for stress cracking of polyethylene. Table 6 lists typical sterile devices and plastic materials used to fabricate them, while Tables 7-9 list the potential effects of sterilization processes on polymeric materials. The effect of gamma irradiation on elastomeric closures has been studied by the Parenteral Drug Association [15]. 

The copolymerisation of ethylene with vinyl acetate (VA) is another method by which the crystallinity of polyethylene can be reduced and a rubbery polymer obtained. The final properties of the copolymer depend on the VA content at a VA level of 50% the copolymer is entirely amorphous, and elastomeric grades generally contain 40-60% VA by weight. The oil resistance of the copolymer is also dependent on the VA content in general, however, this lies between that of SBR and polychloroprene. It is swollen by most organic solvents and not resistant to animal and vegetable oils, but has some resistance to weak acids and alkalis at ambient temperature. 

CPE is the standardized acronym for thermoplastic chlorinated polyethylene. CM is the standardized acronym for elastomeric chlorinated polyethylene. 

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