Ethylene elastomer

Laughner, M. Parikh, D. Walton, K. New developments in metallocene ethylene elastomers for automotive applications. In Polyolefins 2001, Proceedings, Houston, TX, February 25-28, 2001 339-367. 

Paraclor. [Unitoyal] ChMiiated pdy-ethylene elastomer used in wire, cable, hose, mech. goods, extruded, inj. molded, and calendered goods, she sptmge, and for blending. 

J.J. Hemphill et al.. Expanding the product portfolio of ethylene elastomers - ENGAGE polyolefin elastomers for large volume TPO applications, in Proceedings of the SPE-Automotive TPO Global Conference, October 10-12, 2005, Sterling Heights, MI, USA... 

MOR Momeau, G.A., Roth, P.I., and Shultz, A.R., Trifluoronitrosomethane/tetrafluoro-ethylene elastomers dilute solution properties and molecular weight, J. Polym. Sci., 55, 609, 1961. 

Lu YL, Liu L, Shen DY, Yang C, Zhang LQ (2004) Infrared study on in situ polymerization of zinc dimethacrylate in poly(a-octylene-co-ethylene) elastomer. Polym Int 53(6) 802-808... 

The new metallocene ethylene elastomer TPOs now used in the automotive industry possess better low-temperature impact properties and better lifetime durability than soft vinyl plastic. Some new proprietary ethylene-octene copolymer elastomers are being used as TPOs as well, and a new introduction of an ethylene-butene copolymer has been made as well. 

Cincinnati, Oh., 17th.-19th. Oct. 2000, paper 79 MONTE CARLO SIMULATION OF THE PEROXIDE VULCANISATION OF ETHYLENE ELASTOMERS... 

Polyolefins. In these thermoplastic elastomers the hard component is a crystalline polyolefin, such as polyethylene or polypropylene, and the soft portion is composed of ethylene-propylene rubber. Attractive forces between the rubber and resin phases serve as labile cross-links. Some contain a chemically cross-linked rubber phase that imparts a higher degree of elasticity. 

ELASTOMERS,SYNTHETIC - ETHYLENE-PROPYLENE-DIENE RUBBER] (Vol 8)... 

EPM/EPDM compounding [ELASTOMERS, SYNTHETIC - ETHYLENE-PROPYLENE-DIENE RUBBER] (Vol 8) -as insecticide [INSECT CONTROL TECHNOLOGY] (Vol 14)... 

Polyacrylate elastomers find limited use in hydrauhc systems and gasket apphcations because of their superior heat resistance compared to the nitrile mbbers (219,220). Ethylene—acrylate copolymers were introduced in 1975. The apphcations include transmission seals, vibration dampers, dust boots, and steering and suspension seals. Further details and performance comparisons with other elastomers are given in reference 221 (see also Elastomers, SYNTHETIC-ACRYLIC ELASTOTffiRS). 

Acryhc stmctural adhesives have been modified by elastomers in order to obtain a phase-separated, toughened system. A significant contribution in this technology has been made in which acryhc adhesives were modified by the addition of chlorosulfonated polyethylene to obtain a phase-separated stmctural adhesive (11). Such adhesives also contain methyl methacrylate, glacial methacrylic acid, and cross-linkers such as ethylene glycol dimethacrylate [97-90-5]. The polymerization initiation system, which includes cumene hydroperoxide, N,1S7-dimethyl- -toluidine, and saccharin, can be apphed to the adherend surface as a primer, or it can be formulated as the second part of a two-part adhesive. Modification of cyanoacrylates using elastomers has also been attempted copolymers of acrylonitrile, butadiene, and styrene ethylene copolymers with methylacrylate or copolymers of methacrylates with butadiene and styrene have been used. However, because of the extreme reactivity of the monomer, modification of cyanoacrylate adhesives is very difficult and material purity is essential in order to be able to modify the cyanoacrylate without causing premature reaction. 

HDPE, high density polyethylene PP, polypropylene EVA, ethylene—vinyl alcohol SMC, sheet-molding compound ERP, fiber-reinforced plastic LDPE, low density polyethylene PE, polyethylene BMC, bulk mol ding compound TPE, thermoplastic elastomer. 

A series of compounded flame retardants, based on finely divided insoluble ammonium polyphosphate together with char-forming nitrogenous resins, has been developed for thermoplastics (52—58). These compounds are particularly useful as iatumescent flame-retardant additives for polyolefins, ethylene—vinyl acetate, and urethane elastomers (qv). The char-forming resin can be, for example, an ethyleneurea—formaldehyde condensation polymer, a hydroxyethylisocyanurate, or a piperazine—triazine resin. 

Most elastomers can be made iato either opea-ceUed or closed-ceUed materials. Natural mbber, SBR, nitrile mbber, polychloroprene, chlorosulfonated polyethylene, ethylene—propylene terpolymers, butyl mbbers, and polyacrylates have been successfuUy used (4,111,112). 

A unique process for chemical stabili2ation of a ceUular elastomer upon extmsion has been shown for ethylene—propylene mbber the expanded mbber obtained by extmsion is exposed to high energy radiation to cross-link or vulcani2e the mbber and give dimensional stabUity (9). EPDM is also made continuously through extmsion and a combination of hot air and microwaves or radio frequency waves which both activate the blow and accelerate the cure. 

EPDM-Derived Ionomers. Another type of ionomer containing sulfonate, as opposed to carboxyl anions, has been obtained by sulfonating ethylene—propjlene—diene (EPDM) mbbers (59,60). Due to the strength of the cross-link, these polymers are not inherently melt-processible, but the addition of other metal salts such as zinc stearate introduces thermoplastic behavior (61,62). These interesting polymers are classified as thermoplastic elastomers (see ELASTOLffiRS,SYNTHETIC-THERMOPLASTICELASTOLffiRS). 

Many synthetic latices exist (7,8) (see Elastomers, synthetic). They contain butadiene and styrene copolymers (elastomeric), styrene—butadiene copolymers (resinous), butadiene and acrylonitrile copolymers, butadiene with styrene and acrylonitrile, chloroprene copolymers, methacrylate and acrylate ester copolymers, vinyl acetate copolymers, vinyl and vinyUdene chloride copolymers, ethylene copolymers, fluorinated copolymers, acrylamide copolymers, styrene—acrolein copolymers, and pyrrole and pyrrole copolymers. Many of these latices also have carboxylated versions. 

Densities and crystallinities of ethylene—a-olefin copolymers mosdy depend on their composition. The classification ia Table 1 is commonly used (ASTM D1248-48). VLDPE resias are usually further subdivided iato PE plastomers of low crystallinity, 10—20%, with densities ia the range of 0.915—0.900 g/cm, and completely amorphous PE elastomers with densities as low as 0.860 g/cm. ... 

Polypropylene polymers are typically modified with ethylene to obtain desirable properties for specific applications. Specifically, ethylene—propylene mbbers are introduced as a discrete phase in heterophasic copolymers to improve toughness and low temperature impact resistance (see Elastomers, ETHYLENE-PROPYLENE rubber). This is done by sequential polymerisation of homopolymer polypropylene and ethylene—propylene mbber in a multistage reactor process or by the extmsion compounding of ethylene—propylene mbber with a homopolymer. Addition of high density polyethylene, by polymerisation or compounding, is sometimes used to reduce stress whitening. In all cases, a superior balance of properties is obtained when the sise of the discrete mbber phase is approximately one micrometer. Examples of these polymers and their properties are shown in Table 2. Mineral fillers, such as talc or calcium carbonate, can be added to polypropylene to increase stiffness and high temperature properties, as shown in Table 3. 

Organic peroxides are used in the polymer industry as thermal sources of free radicals. They are used primarily to initiate the polymerisation and copolymerisation of vinyl and diene monomers, eg, ethylene, vinyl chloride, styrene, acryUc acid and esters, methacrylic acid and esters, vinyl acetate, acrylonitrile, and butadiene (see Initiators). They ate also used to cute or cross-link resins, eg, unsaturated polyester—styrene blends, thermoplastics such as polyethylene, elastomers such as ethylene—propylene copolymers and terpolymers and ethylene—vinyl acetate copolymer, and mbbets such as siUcone mbbet and styrene-butadiene mbbet. 

Most elastomers that are used for nylon modification contain a small amount of maleic anhydride (0.3 to 2%). In the melt blending process, these elastomers react with the primary amine end groups in nylon, giving rise to nylon grafted elastomers. These grafts reduce the interfacial tension between the phases and provide steric stabili2ation for the dispersed mbber phase. Typically, thermally stable, saturated mbbers such as EPR, EPDM, and styrene—ethylene/butylene—styrene (SEBS) are used. 

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