Vulcanates, thermoplastic

The ability to make PE with properties that fall outside these limitations would lead to a tremendous expansion of uses for this polymer, for example replacing flexible polyvinylchloride (f-PVC), which cannot be incinerated or recycled, thermoplastic polyurethanes (TPUs), or thermoplastic vulcanates (TPVs). 

TPEs are blends of various amorphous rubbers such as ethylene-propylene and of polyolefin semicrystalline plastics such as PP. They are part of the family of TP olefins (TPOs). TPOs are mechanical blends consisting of a hard plastic and softer rubber. They are considered different from blends that are dynamically thermoplastic vulcanized (TPV) a process in which the elastomer phase is cured during mixing of the polymers.84 94... 

The blends of EPDM terpolymers and isotactic PP with curing agents, such as peroxide, phenol resins, and sulfur, are termed as thermoplastic vulcanized elastomer (TPV) since the rubber domains are vulcanized. Polyolefin copolymers, such as random copolymer of propylene with ethylene, copolymers of other olefins, elastomeric PP, and elastomeric PE, are developed with recent advances of... 

The effect of compatabilizer (MAPE) to eliminate discontinuity in the flow curve of the thermoplastic vulcanized (PE/PB) was studied. Various concentration of the compatabilizer (0, 2, 4, 6, 8 and 10 wt/wt%) were tested. It was shown that the complete elimination of discontinuity which caused by the pressure oscillation inside the die during the polymer melt flow. The presence of the MAPE will act as compatabilizer between the two polymer chain and both the 8% and 10% can achieved the complete chain interaction and the blend will be completely miscible and act as one phase, while the 8% cannot offer the sufficient adhesion forces between the polymer and the die... 

Polymer melt instabilities Polymer rheology Thermoplastic vulcanized... 

Peroxides can be used to promote crosslinking of a rubber as is done in dynamic vulcanization. Dynamic vulcanization is usually done in an extruder and is the process of selectively crosslinking rubber during its melt mixing with a molten thermoplastic such as polypropylene. This produces thermoplastic vulcanates, often referred to as TPVs [16]. Peroxides are also used to provide grafting reactions. For example, polypropylene, maleic anhydride, and a peroxide initiator in a twin-screw extruder give a graft polypropylene [17]. These polymers can have improved properties such as improved adhesion. 

The effect of the injection molding process conditions (melt and mold temperatures, holding/packing pressure and injection velocity) over the adhesion resistance of two overmolded materials was studied. The materials used were a Thermoplastic Vulcanized Elastomer (TPV) (Santoprene 8211-55) and a Polypropylene (PP) (Moplen HP501H). The measurement of the adhesion resistance was done by Tensile Test and it was observed that the melt and mold temperature are the parameters that affect in greater degree the adhesion resistance. 

At this point in the process, thermoplastic and chlorosulfonated polyethylene (CSPE) membranes are complete and are ready for packaging. In the case of ethylene—propylene—diene monomer (EPDM), the curing step occurs before the membrane is ready for packaging. The curing process is accomphshed by placing the membrane in a large vulcanizer where the material is heated under pressure to complete the cure. 

Ethylene—Propylene Rubber. Ethylene and propjiene copolymerize to produce a wide range of elastomeric and thermoplastic products. Often a third monomer such dicyclopentadiene, hexadiene, or ethylene norbomene is incorporated at 2—12% into the polymer backbone and leads to the designation ethylene—propylene—diene monomer (EPDM) mbber (see Elastomers, synthetic-ethylene-propylene-diene rubber). The third monomer introduces sites of unsaturation that allow vulcanization by conventional sulfur cures. At high levels of third monomer it is possible to achieve cure rates that are equivalent to conventional mbbers such as SBR and PBD. Ethylene—propylene mbber (EPR) requires peroxide vulcanization. 

The more important grades of thermoplastic natural mbber, which fall into the olefinic class of thermoplastic elastomers, are prepared with the natural mbber phase partially cross-linked during blending, a process known as dynamic vulcanization. The hardness of the soft blends is controlled by the natural mbber content, and typical properties of those of 50—90 hardness (Shore A) are shown in Table 7. 

An entirely new concept was iatroduced iato mbber technology with the idea of "castable" elastomers, ie, the use of Hquid, low molecular-weight polymers that could be linked together (chain-extended) and cross-linked iato mbbery networks. This was an appealing idea because it avoided the use of heavy machinery to masticate and mix a high viscosity mbber prior to mol ding and vulcanization. In this development three types of polymers have played a dominant role, ie, polyurethanes, polysulftdes, and thermoplastic elastomers. 

Thermoplastic Elastomers. These represent a whole class of synthetic elastomers, developed siace the 1960s, that ate permanently and reversibly thermoplastic, but behave as cross-linked networks at ambient temperature. One of the first was the triblock copolymer of the polystyrene—polybutadiene—polystyrene type (SheU s Kraton) prepared by anionic polymerization with organoHthium initiator. The stmcture and morphology is shown schematically in Figure 3. The incompatibiHty of the polystyrene and polybutadiene blocks leads to a dispersion of the spherical polystyrene domains (ca 20—30 nm) in the mbbery matrix of polybutadiene. Since each polybutadiene chain is anchored at both ends to a polystyrene domain, a network results. However, at elevated temperatures where the polystyrene softens, the elastomer can be molded like any thermoplastic, yet behaves much like a vulcanized mbber on cooling (see Elastomers, synthetic-thermoplastic elastomers). 

Because of increased production and the lower cost of raw material, thermoplastic elastomeric materials are a significant and growing part of the total polymers market. World consumption in 1995 is estimated to approach 1,000,000 metric tons (3). However, because the melt to soHd transition is reversible, some properties of thermoplastic elastomers, eg, compression set, solvent resistance, and resistance to deformation at high temperatures, are usually not as good as those of the conventional vulcanized mbbers. AppHcations of thermoplastic elastomers are, therefore, in areas where these properties are less important, eg, footwear, wine insulation, adhesives, polymer blending, and not in areas such as automobile tires. 

Multiblock Copolymers. Replacement of conventional vulcanized mbber is the main appHcation for the polar polyurethane, polyester, and polyamide block copolymers. Like styrenic block copolymers, they can be molded or extmded using equipment designed for processing thermoplastics. Melt temperatures during processing are between 175 and 225°C, and predrying is requited scrap is reusable. They are mostiy used as essentially pure materials, although some work on blends with various thermoplastics such as plasticized and unplasticized PVC and also ABS and polycarbonate (14,18,67—69) has been reported. Plasticizers intended for use with PVC have also been blended with polyester block copolymers (67). 

Subsequently, much improved thermoplastic polyolefin rubbers were obtained by invoking a technique known as dynamic vulcanisation. This process has been defined (Coran, 1987) as the process of vulcanizing elastomer during its intimate melt-mixing with a non-vulcanizing thermoplastic polymer. Small elastomer droplets are vulcanized to give a particulate... 

Partially vulcanized EPDM/Poly- propylene blend" Completely vulcanized EPDM/Poly- propylene blend Neoprene vulcanizate Ester-ether copolymer thermoplastic elastomer ... 

Thermoplastic polyurethane (TPU) is a type of synthetic polymer that has properties between the characteristics of plastics and rubber. It belongs to the thermoplastic elastomer group. The typical procedure of vulcanization in rubber processing generally is not needed for TPU instead, the processing procedure for normal plastics is used. With a similar hardness to other elastomers, TPU has better elasticity, resistance to oil, and resistance to impact at low temperatures. TPU is a rapidly developing polymeric material. 

Compatibilization along with dynamic vulcanization techniques have been used in thermoplastic elastomer blends of poly(butylene terephthalate) and ethylene propylene diene rubber by Moffett and Dekkers [28]. In situ formation of graft copolymer can be obtained by the use of suitably functionalized rubbers. By the usage of conventional vulcanizing agents for EPDM, the dynamic vulcanization of the blend can be achieved. The optimum effect of compatibilization along with dynamic vulcanization can be obtained only when the compatibilization is done before the rubber phase is dispersed. 

In addition to dynamic vulcanization, the technological compatibilization technique was also adopted by Coran and Patel [34] to obtain thermoplastic vulcanizate having good mechanical integrity and elastic recovery. 

Thermoplastic elastomers are materials that have the properties of vulcanized rubbers but can be processed by techniques associated with thermoplastics. The commercial importance of TPEs is due to their superior processing properties and economic advantages over conventional rubbers and plastics. TPEs from rubber-plastic blends became important because they combine the superior processability of thermoplastics and the... 

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