Thermoplastic polyolefin elastomers TPOs

Blends of EPDM rubbers with polypropylene in suitable ratios have been marketed as thermoplastic elastomers (TPE), also commercially known as thermoplastic polyolefin elastomers (TPO). These heterophasic polymers, characterized by thermoreversible interaction among the polymeric chains, belong to a broad family of olefinic alloys that can now be produced directly during the polymerization phase, unlike blended TPE and TPO, and various compositions (with various compounding additives) can be formulated which are primarily tailored to meet different requirements of most of car applications. The TPE-based synthetic leather and foam sheets are typical examples. 

Polypropylene (PP) in various forms (filled, unfilled, reinforced, rubber blended) finds the greatest usage of all automotive plastics. Its consumption is likely to accelerate as a result of new laws requiring recyclability, and because of the weight and cost reductions it offers. New fabrication techniques may also contribute to growth. For example, the monomaterial sandwich construction techniques developed by fabricators yield rugged and lightweight PP-based instrument and door panels. These parts consist of a sandwich of reinforced or neat PP substrate, a cross-linked PP foam, and a thermoplastic polyolefin elastomer (TPO) cover. 

A thermoplastic polyolefin elastomer TPO-g-PLA was prepared by grafting PLA onto maleic anhydride-functionalized TPO in the presence of 4-dimethyl aminopyridine (DMAP). A high reaction temperature and a high DMAP concentration resulted in the polymerization of PLA. These copolymers were used as a compatibilizer for PLA/TPO blends. An increase in concentration of this copolymer from 0% to 2.5% resulted in an increase in elongation at break and tensile toughness of the blends [94]. 

Poly(ethylene-octene) Copolymer/PLA Blends Poly(ethylene-octene) copolymer, a thermoplastic polyolefin elastomer (TPO), was melt blended with PLA at a ratio of 20/ 80 wt% [10]. The difference in polarities of the two polymers led to thermodynamic immiscibility and phase separation of the final blends as determined by the Molau test. Therefore, a copolymer of TPO-gra//-PLA (TPO-PLA synthesized via functionalization of TPO and MA with benzoyl peroxide (BPO), followed by esterification of the MA-functionalized TPO (TPO-MAH) with PLA using 4-dimethylaminopyridine (DMAP) as a catalyst) was introduced to improve the compatibility of the TPO/PLA blends. The use of 5 wt% TPO-... 

If polypropylene is too hard for the purpose envisaged, then the user should consider, progressively, polyethylene, ethylene-vinyl acetate and plasticised PVC. If more rubberiness is required, then a vulcanising rubber such as natural rubber or SBR or a thermoplastic polyolefin elastomer may be considered. If the material requires to be rubbery and oil and/or heat resistant, vulcanising rubbers such as the polychloroprenes, nitrile rubbers, acrylic rubbers or hydrin rubbers or a thermoplastic elastomer such as a thermoplastic polyester elastomer, thermoplastic polyurethane elastomer or thermoplastic polyamide elastomer may be considered. Where it is important that the elastomer remain rubbery at very low temperatures, then NR, SBR, BR or TPO rubbers may be considered where oil resistance is not a consideration. If, however, oil resistance is important, a polypropylene oxide or hydrin rubber may be preferred. Where a wide temperature service range is paramount, a silicone rubber may be indicated. The selection of rubbery materials has been dealt with by the author elsewhere. ... 

In addition to the two-phase TPEs, two new technologies have emerged. They are the metallocene-catalyzed polyolefin plastomers (POPs, the name given to Exxon s EXACT product line) and polyolefin elastomers (POEs, DuPont Dow Elastomer s ENGAGE), and reactor-made thermoplastic polyolefin elastomers (R-TPOs). These new types of TPEs are often called metallocene elastomers-TPEs (MEs-TPEs) [87]. The new POPs and POEs are essentially very low-molecular-weight-Unear low-density PEs (VLMW-LLDPE). These new-generation TPEs exhibit mbber-like properties and can be processed on... 

Polyolefins, PO. First impact modification of PO, by addition of elastomers, was patented independently by Bayer A.-G. and Standard Oil Co. in 1937. The isotactic polypropylene, PP, was commercialized in 1957, and its first blends (with polyisobutylene, PIB, and polyethylene, PE) were patented in 1958. In 1960, du Pont started manufacturing ethylene-propylene, EPR, and three years later ethylene-propylene-diene, EPDM, copolymers [Gresham and Hunt, I960]. The first patent on impact modification of PP by addition of EPR dates from 1960. Direct reactor blending of PE/PP/EPR resulting in a thermoplastic polyolefin, R-TPO, dates from 1979. The newest (introduced in 1992) single-site metallocene catalysts generate polymers with controlled tacticity, co-monomer sequences, molecular... 

Thermoplastic Polyolefin n (TPO) Any of a group of elastomers produced by either of two processes. In one, polypropylene is melt-blended with from 15% to 85% of terpolymer elastomer, ethylenepropylene rubber, or styrene-butadiene rubber. In the other, propylene is copolymerized with ethylene-propylene elastomer in a series of reactions. The smaller elastomeric domains obtained in the latter process are claimed to provide improved properties over the blended materials. 

Figure 3. Hardness range of selected polymers and TPEs. TPO - thermoplastic polyolefin elastomer all other abbreviations are disclosed in the text...

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. 

Obviously, there exists severe interplastics competition, e.g. PP vs. ABS, clarified PP vs. PS, PA, PVC, HDPE and PS (Table 10.7). A wide range of cross-linked and thermoplastic elastomer applications, from footware to automotive parts and toothbrushes, are adopting new metallocene-catalysed polyolefin elastomers (POEs). These low-density copolymers of ethylene and octene were first accepted as impact modifiers for TPOs, but now displace EPDM, (foamed) EVA, flexible PVC, and olefinic thermoplastic vulcanisates (TPVs). Interpolymer competition may also result from... 

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. 

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