Terpolymers of ethylene, vinyl

However, a method to improve the flow properties of such fuel oils of animal or vegetable origin, has been developed (26). This consists in adding a EVA copolymer or a comb polymer based on methyl acrylate and a-olefins. In addition, terpolymers of ethylene, vinyl acetate and isobutylene have been found to be useful as cold flow improvers (29). 

TVy blending with any one of a multitude of additives, PVC can be transformed into a broad spectrum of resins ranging from highly plasticized to impact resistant. The use of polymeric plasticizers has attracted a great deal of attention because they provide superior permanence in physical properties over their low molecular weight counterparts. Recently a terpolymer of ethylene, vinyl acetate, and carbon monoxide was reported to be miscible with PVC (1,2). The system is of interest because blends of PVC and ethylene-vinyl acetate copolymers range from incompatible to miscible, depending on the content of vinyl acetate in the copolymer (3,4,5). We have therefore undertaken x-ray,... 

Terpolymers of ethylene, vinyl acetate and N15AK ac e prepared by adding the lal er two inder constant ethylene pressure into an initiated emulsifier solution containing polyvinyl alcohol, controlling the amount of unpolymerised vinyl acetate at any one time to be under This method enables ethylene to be copolymv... 

Ethylene-vinyl acetate (EVA) polymers (containing 65%-70% by weight of vinyl acetate) are of industrial interest as high-molecular weight plasticizers for PVC, mainly because of their low cost. A polymeric plasticizer PB-3041 available from Du Pont allows the preparation of a highly permanent plasticized PVC formulation. It is believed to be a terpolymer of ethylene, vinyl, acetate, and carbon monoxide. Also, butylene terephthalate-tetrahydrofuran block copolymers, with the trade name of Hytrel (Du Pont), are used as excellent permanent plasticizers of PVC. 

These blends with LDPE are sometimes reported as incompatible [110], at other times praised for their benefits. For example, addition of 10% of LDPE more than tripled impact strength [205] and LDPE has been reported to improve ultimate tensile strength and elongation, impact strength, water resistance, and dimensional stability [108,109]. In one study, blends were compatibilized by adding a terpolymer of ethylene/vinyl alcohol/vinyl mercaptoacetate, which reduced domain size and improved mechanical properties [202]. 

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. 

The isoprene units in the copolymer impart the ability to crosslink the product. Polystyrene is far too rigid to be used as an elastomer but styrene copolymers with 1,3-butadiene (SBR rubber) are quite flexible and rubbery. Polyethylene is a crystalline plastic while ethylene-propylene copolymers and terpolymers of ethylene, propylene and diene (e.g., dicyclopentadiene, hexa-1,4-diene, 2-ethylidenenorborn-5-ene) are elastomers (EPR and EPDM rubbers). Nitrile or NBR rubber is a copolymer of acrylonitrile and 1,3-butadiene. Vinylidene fluoride-chlorotrifluoroethylene and olefin-acrylic ester copolymers and 1,3-butadiene-styrene-vinyl pyridine terpolymer are examples of specialty elastomers. 

At room temperature, PE is a semi-crystalline plastomer (a plastic which on stretching shows elongation like an elastomer), but on heating crystallites melt and the polymer passes through an elastomeric phase. Similarly, by hindering the crystallisation of PE (that is, by incorporating new chain elements), amorphous curable rubbery materials like ethylene propylene copolymer (EPM), ethylene propylene diene terpolymer (EPDM), ethylene-vinyl acetate copolymer (EVA), chlorinated polyethylene (CM), and chlorosulphonated polyethylene (CSM) can be prepared. 

Physical Properties of Blends of Poly(vinyl Chloride) and a Terpolymer of Ethylene... 

The compatibility of blends of poly (vinyl chloride) (PVC) and a terpolymer (TP) of ethylene, vinyl acetate, and carbon monoxide was investigated by dynamic mechanical, dielectric, and calorimetric studies. Each technique showed a single glass transition and that transition temperature, as defined by the initial rise in E" at 110 Hz, c" at 100 Hz, and Cp at 20°C/min, agreed to within 5°C. PVC acted as a polymeric diluent which lowered the crystallization temperature, Tc, of the terpolymer such that Tc decreased with increasing PVC content while Tg increased. In this manner, terpolymer crystallization is inhibited in blends whose value of (Tc — Tg) was negative. Thus, all blends which contained 60% or more PVC showed little or no crystallinity unless solvent was added. 

Studies of ethylene-vinyl aromatic monomer polymerizations continue to be published. Chung and Lu reported the synthesis of copolymers of ethylene and P-methylstyrene [28] and the same group extended these studies to produce and characterize elastomeric terpolymers which further include propylene and 1-octene as the additional monomers [29,30]. Returning to the subject of alternative molecular architectures for copolymers, Hou et al. [31] has reported the ability of samarium (II) complexes to copolymerize ethylene and styrene into block copolymers. 

From three-component free-radical-initiated polymerization studies of ethylene, vinyl chloride, and MA, it was concluded that MA can undergo alternating copolymerization with vinyl chloride. Regardless of the initial monomer composition, a terpolymer was obtained with 50 mol % vinyl chloride and ethylene combined with 50 mol % MA. A CTC has been suggested to play a role in the copolymerization. However, the fact that... 

In the case of EVOH being used as an interlayer with polyethylene or polystyrene, it is necessary to use additional adhesive layers such as an ethylene-vinyl acetate-maleic anhydride terpolymer (e.g. Orevac— Atochem). 

In the following decades, homo-, co- and terpolymers of VAM with other vinyl esters, (meth)acrylates, and ethylene were developed to give thermoplastic materials with tailored properties that are nowadays produced as solid resins, aqueous dispersions and dispersible powders. 

New terpolymers of vinyl acetate with ethylene and carbon monoxide have been prepared and their uses as additives to improve the curing and flexibility of coating resins, eg, nitrocellulose, asphalt, phenolics, and polystyrene, have been described (130—132). Vinyl acetate and vinylidene cyanide form highly alternating copolymers. 

Internal plasticizers are synthesized by copolymerization of suitable monomers. Polymeric non-extractable plasticizers, mostly copolymers having substantially lower glass transition temperatures due to the presence of plasticizing ( soft ) segments such as poly(ethylene-co-vinyl acetate) with approximately 45 % vinylacetate content, ethylene-vinyl acetate-carbon monooxide terpolymer, or chlorinated PE, are available for rather special applications in medicinal articles (Meier, 1990). In this case, the performance of the internally plasticized polymers is the principal advantage. However, copolymerization may account for worse mechanical properties. A combination with external plasticizers may provide an optimal balance of properties. For example, food contact products made from poly(vinylidene chloride) should have at most a citrate or sebacate ester based plasticizers content of 5 % and at most 10 % polymeric plasticizers. 

Poly[styrene-co-(2-hydroxy-4 -vinylbenzophenone)] was less efficient in PS than 2-hydroxy-4-methoxybenzophenone [334]. Similarly, PE films doped with 4-dodecyloxy-2-hydroxybenzophenone (0.1 mol%) were more stable than PE doped with copolymers of ethylene with polymerisable benzophenones having a comparable content of chromophores [54]. The efficiency of a SAN type LS, a terpolymer of 2-hydroxy-4-(4-vinylbenzyloxy)benzophenone with acrylonitrile and styrene did not exceed that of conventional LS [84]. No efficiency loss of 2-hydroxy-4-methacryloyloxybenzophenone in ABS was observed after bonding into a terpolymer with styrene and acrylonitrile. The homopolymer was slightly inferior to both the monomer and terpolymer [84]. A better protection of PP was provided by poly[(2-hydroxy-3-allyl-4-methoxyphenylbenzophenone)-co-dibutyl maleate] than with 2-hydroxy-3-allyl-4-methoxybenzophenone [335] (stabilization tests were performed in the presence of phenolic antioxidants). A comparable or better light stabilizing efficiency of poly[vinyl acetate-co-(5-methylacryloyloxy salicylate)] or poly(2-allylphenyl salicylate-co-dioctyl maleate) than that of alkyl-phenyl salicylates was observed in polyolefins [335]. 

Co-polymerization of ethylene with cyclic dienes such as 1,3-cyclopentadiene, dicyclopentadiene, and 4-vinyl-l-cyclohexene using rac-C2H4(Ind)2ZrCl2 showed that dicyclopentadiene was the most reactive co-monomer. 1,3-Cyclopentadiene rapidly dimerizes to dicyclopentadiene, and thus ethylene/l,3-cyclopentadiene co-polymerization actually resulted in ethylene/l,3-cyclopentadiene terpolymers with dicyclopentadiene. Co-polymers with more than 9mol% of the co-monomer did not show a melt transition.1058... 

Figure 3 shows the solubility characteristics of the vinyl acetate copolymers in MEK note the improved solubility over the homopolymers of vinyl chloride. Because these copolymers are still significantly less soluble than the metal adhesion terpolymers, one manufacturer has produced a copolymer not based on vinyl acetate (see Figure 3, high solubility copolymers). This copolymer is described in more detail in Figure 13. Copolymers are also available based on vinyl chloride-trifluorochloro-ethylene and vinyl chloride-vinylidene chloride.

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