Thermoplastic polyolefin blends

Thermoplastic polyolefin blends can be produced as quite soft materials (as low as 55 Shore A) or as harder (above 95 Shore A), flexible products. They are particularly useful when a combination of good weatherabi1ity and rubbery behavior is required. Applications include automotive parts, weather stripping, hose, and sporting goods. Because of their good dielectric and insulating properties, polyolefin blends may be particularly useful in wire and cable insulation. 

Block Copolymers Thermoplastic Polyolefins (Blends, partly crosslinked)... 

T.L. Wong, C.M.F. Barry, S.A. Oiroth, The effects of filler size on the properties of thermoplastic polyolefin blends. J. Vinyl Addit. Technol. 5, 235-240 (1999)... 

Thermoplastic polyolefin blend paintable without necessity of surface pretreatment STRUCTURE Co-continuous... 

V.A. Dang, D. Dong, T.T.M. Phan, and C.Q. Song, Compatibiliz-ing agent for engineering thermoplastic/polyolefin blend, US Patent 6 887 940, assigned to Basell Poliolefine Italia S.p.A. (Milan, IT), May 3,2005. 

In the early stages of development of polypropylene rubbers, particularly butyl rubber, were used to reduce the brittleness of polypropylene. Their use declined for some years with the development of the polypropylene copolymers but interest was greatly renewed in the 1970s. This interest has been centred largely around the ethylene-propylene rubbers which are reasonably compatible in all proportions with polypropylene. At first the main interest was with blends in which the rubber content exceeded 50% of the blend and such materials have been designated as thermoplastic polyolefin elastomers (discussed in Section 11.9.1). There is also increasing interest in compounds with less than 50% rubber, often referred to as elastomer-modified thermoplastics. It is of interest to note... 

In addition to the somewhat sophisticated triblock thermoplastic elastomers described above, mention should be made of another group of thermoplastic diene rubbers. These are physical blends of polypropylene with a diene rubber such as natural rubber. These may be considered as being an extension to the concept of thermoplastic polyolefin rubbers discussed in Section 11.9.1 and although extensive experimental work has been carried out with these materials they do not yet appear to have established themselves commercially. 

These rubbers are now also being blended on a large scale with polyolefin plastics, particularly polypropylene, to produce a range of materials which at one extreme are tough plastics and at the other the so-called thermoplastic polyolefin rubbers (TPORs) (.see Section 11.9.1). 

Although the elastomer phase is essentially in particulate form, the tensile strength of the blend can be increased five-fold by increasing the cross-link density from zero to that conventionally used in vulcanisation processes, whilst tension set may be reduced by over two-thirds. Since the thermoplastic polyolefin phase may be completely extracted by boiling decalin or xylene, there is apparently no covalent chemical bonding of elastomer and thermoplastic phases. 

A manufacturer considering using a thermoplastic elastomer would probably first consider one of the thermoplastic polyolefin rubbers or TPOs, since these tend to have the lowest raw polymer price. These are mainly based on blends of polypropylene and an ethylene-propylene rubber (either EPM or EPDM) although some of the polypropylene may be replaeed by polyethylene. A wide range of blends are possible which may also contain some filler, oil and flame retardant in addition to the polymers. The blends are usually subject to dynamic vulcanisation as described in Section 11.9.1. 

Currently, important TPE s include blends of semicrystalline thermoplastic polyolefins such as propylene copolymers, with ethylene-propylene terepolymer elastomer. Block copolymers of styrene with other monomers such as butadiene, isoprene, and ethylene or ethylene/propy-lene are the most widely used TPE s. Styrene-butadiene-styrene (SBS) accounted for 70% of global styrene block copolymers (SBC). Currently, global capacity of SBC is approximately 1.1 million tons. Polyurethane thermoplastic elastomers are relatively more expensive then other TPE s. However, they are noted for their flexibility, strength, toughness, and abrasion and chemical resistance. Blends of polyvinyl chloride with elastomers such as butyl are widely used in Japan. ... 

Thermoplastic polyolefin rubbers are usually blends based on polypropylene and ethylene-propylene rubbers. They are not resistant to hydrocarbons. 

A route to compatibility involving ionomers has been described recently by Eisenberg and coworkers [250-252]. The use of ionic interactions between different polymer chains to produce new materials has gained tremendous importance. Choudhury et al. [60] reported compatibilization of NR-polyolefin blends with the use of ionomers (S-EPDM). Blending with thermoplastics and elastomers could enhance the properties of MPR. The compatibility of copolyester TPE, TPU, flexible PVC, with MPR in aU proportions, enables one to blend any combination of these plastics with MPR to cost performance balance. Myrick has reported on the effect of blending MPR with various combinations and proportions of these plastics and provided a general guideline for property enhancement [253]. 

Roy Choudhury N., De P.P., and Bhowmick A.K., Thermoplastic elastomeric natural rubber-polyolefin blends. Thermoplastic Elastomers from Rubber Plastic Blend (De S.K. and Bhowmick A.K., eds.), Ellis Horwood, London, 1990, 11. 

Roy Choudhury N. and Bhowmick A.K., Compatibilization of natural rubber-polyolefin thermoplastic elastomeric blends by phase modification, J. Appl. Polym. Sci., 30, 1091, 1989. 

Kresge E.N., Polyolefin thermoplastic elastomer blends. Rubber Chem. TechnoL, 64, 469, 1991. 

Choudhury, N.R. and Bhowmick, A.K., Strength of thermoplastic elastomers from rubber-polyolefin blends, J. Mater. Sci., 25, 161, 1990. 

In addition to the polyolefin blends designed for thermoplastic elastomer applications, a great deal of interest also has centered on other kinds of blends of polyolefins as has been reviewed recently (see chapter 21 of Ref. 10 by Plochocki). In a recent paper (84), we showed that blends involving polypropylene-high density polyethylene-low density polyethylene in various proportions and combinations exhibit additivity of tensile strength however, there are serious losses in ductility in some cases such that the blends are less ductile than either pure component. It is interesting to note, however, that these losses in ductility can largely be restored by addition of rather small amounts of an amorphous ethylene-propylene rubber (84). 

Plastic types are variable, ranging from flexible to rigid and from thermoplastic to thermoset. Because of these variations, the type of coating applied to them also varies, depending on cure response, solvent sensitivity, and modulus. The type of coating also depends upon the end use of the coated plastic. For example, topcoats can be applied directly to the plastic without the use of a conductive primer if two-toning or blackout areas are not part of the styling latitude. Adhesion promoters also are often utilized if a particularly difficult-to-adhere-to plastic is encountered (i.e., polypropylenes or thermoplastic polyolefins (TPOs), a blend of elastomer and olefin). 

TPOs are basically two-component elastomer systems consisting of an elastomer finely dispersed in a thermoplastic polyolefin (such as polypropylene). The thermoplastic polyolefin is the major component. Thermoplastic elastomers (TPEs) include TPOs, TPVs (thermoplastic vulcanizates), etc. Properties of TPOs depend upon the types and amounts of polymers used, the method by which they are combined, and the use of additives such as oils, fillers, antioxidants, and colors. Blends and reactor-made products compete primarily with other TPEs and metals. There are vulcanizates (TPVs) that have higher elastomeric properties. They compete primarily with TS elastomers. 

Thermoplastic polyolefins (TPOs) are based on blends of polypropylene with ethylene-propylene rubbers. Many perform well as hose, exterior automotive trim and bumpers without chemical linking of the main polymeric components. 

The first reactor-type thermoplastic polyolefin (R-TPO) was LLDPE/PP [Yamazaki and Eujimaki, 1970, 1972]. The three-component R-TPO s (PE with PP and EPR) soon followed [Strametz et al, 1975]. PE was also polymerized in the presence of active catalyst and an olefinic copolymer [Morita and Kashiwa, 1981]. Blending amorphous co-polyolefins with crystalline PO s (HDPE, LLDPE, PP), and a filler resulted in moldable blends, characterized by excellent sets of properties [Davis and Valaitis, 1993, 1994]. Blends of polycycloolefin (PCO) with a block copolymer (both polymerized in metallocene catalyzed process) and PE, were reported to show outstanding properties, viz. strength, modulus, heat resistance and toughness [Epple and Brekner, 1994]. 

Reactor-blends PE with PP and EPR reactor- thermoplastic polyolefin, R-TPO Yamazaki Eujimaki, 1970... 

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