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Ethylene vinyl acetate plastic

VCEVAC (Vinyl chloride)-ethylene-(vinyl acetate) plastic... [Pg.75]

Other Films. Although commercially less important than polyethylenes and polypropylenes, a number of other plastic films are in commercial use or development for special appHcations, including ethylene—vinyl acetate, ionomer, and polyacrylonitrile [25014-41-9]. [Pg.452]

Plasticizers. Monomeric (mol wt 250—450) plasticizers (qv) are predominantiy phthalate, adipate, sebacate, phosphate, or trimeUitate esters. Organic phthalate esters like dioctyl phthalate (DOP) are by far the most common plasticizers in flexible PVC. Phthalates are good general-purpose plasticizers which impart good physical and low temperature properties but lack permanence in hot or extractive service conditions and are therefore sometimes called migratory plasticizers. Polymeric plasticizers (mol wt up to 5000 or more) offer an improvement in nonmigratory permanence at a sacrifice in cost, low temperature properties, and processibiHty examples are ethylene vinyl acetate or nitrile polymers. [Pg.327]

The use of TAG as a curing agent continues to grow for polyolefins and olefin copolymer plastics and mbbers. Examples include polyethylene (109), chlorosulfonated polyethylene (110), polypropylene (111), ethylene—vinyl acetate (112), ethylene—propylene copolymer (113), acrylonitrile copolymers (114), and methylstyrene polymers (115). In ethylene—propylene copolymer mbber compositions. TAG has been used for injection molding of fenders (116). Unsaturated elastomers, such as EPDM, cross link with TAG by hydrogen abstraction and addition to double bonds in the presence of peroxyketal catalysts (117) (see Elastol rs, synthetic). [Pg.88]

The very low density materials (VLDPEs) introduced in the mid-1980s are generally considered as alternatives to plasticised PVC (Chapter 12) and ethylene-vinyl acetate (EVA) plastics (see Chapter 11). They have no volatile or extractable plasticisers as in plasticised PVC nor do they have the odour or moulding problems associated with EVA. Whilst VLDPE materials can match the flexibility of EVA they also have better environmental stress cracking resistance, improved toughness and a higher softening point. [Pg.227]

Whilst vinyl acetate is reluctant to copolymerise it is in fact usually used today in copolymers. Two of particular interest to the plastics industry are ethylene-vinyl acetate (Chapter 11) and vinyl chloride-vinyl acetate copolymers (Chapter 12). In surface coatings internal plasticisation to bring the Tg to below ambient temperatures and thus facilitate film forming is achieved by the use of ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate and dialkyl maleates and fumarates. [Pg.397]

Among the different pressure sensitive adhesives, acrylates are unique because they are one of the few materials that can be synthesized to be inherently tacky. Indeed, polyvinylethers, some amorphous polyolefins, and some ethylene-vinyl acetate copolymers are the only other polymers that share this unique property. Because of the access to a wide range of commercial monomers, their relatively low cost, and their ease of polymerization, acrylates have become the dominant single component pressure sensitive adhesive materials used in the industry. Other PSAs, such as those based on natural rubber or synthetic block copolymers with rubbery midblock require compounding of the elastomer with low molecular weight additives such as tackifiers, oils, and/or plasticizers. The absence of these low molecular weight additives can have some desirable advantages, such as ... [Pg.485]

Coran and Patel [33] selected a series of TPEs based on different rubbers and thermoplastics. Three types of rubbers EPDM, ethylene vinyl acetate (EVA), and nitrile (NBR) were selected and the plastics include PP, PS, styrene acrylonitrile (SAN), and PA. It was shown that the ultimate mechanical properties such as stress at break, elongation, and the elastic recovery of these dynamically cured blends increased with the similarity of the rubber and plastic in respect to the critical surface tension for wetting and with the crystallinity of the plastic phase. Critical chain length of the rubber molecule, crystallinity of the hard phase (plastic), and the surface energy are a few of the parameters used in the analysis. Better results are obtained with a crystalline plastic material when the entanglement molecular length of the... [Pg.641]

Plasticization Polycaprolactone, polyurethanes, nitrile rubber, ethylene-vinyl acetate, copolyester, chlorinated polyoxymethylenes (acetals)... [Pg.347]

DWP design with plastics EVA ethylene-vinyl acetate... [Pg.650]

ISO 4613-1 1993 Plastics - Ethylene/vinyl acetate (E/VAC) moulding and extrusion materials - Part 1 Designation and specification ISO 4613-2 1995 Plastics - Ethylene/vinyl acetate (E/VAC) moulding and extrusion materials - Part 2 Preparation of test specimens and determination of properties ISO 8985 1998 Plastics - Ethylene/vinyl acetate copolymer (EVAC) thermoplastics -Determination of vinyl acetate content... [Pg.289]

BXL Plastics ERP Division is to introduce new grades of antistatic and conductive closed-cell crosslinked PE and ethylene copolymer foam at the Internepcon Exhibition to meet a growing demand from the electronics industry, for ways of minimising the effect of static electricity on circuits embodying static-sensitive devices, particularly using metal oxide/silicone technology. Very brief details are noted of Evazote C conductive closedcell, crosslinked ethylene-vinyl acetate copolymer foam. [Pg.115]

New modified polymeric electrodes selective to procaine and other local anaesthetic compounds were reported [72]. The electrode was constructed by incorporating the ion-pair complex of procaine with tungsto-phosphoric acid into ethylene-vinyl acetate copolymer. Best results were obtained with 1 1 nitrobenzene-dioctyl phthalate as a plasticizer. The calibration graph was linear fi om 18 p to 10 mM of procaine. When these electrodes were applied to the determination of the drug in pharmaceutical formulations, the recoveries were found to be quantitative. [Pg.423]

Some authors took advantage of the reactivity of polymers with ozone to recycle some peculiar plastic wastes coming from different origins. In this way, Fargere [155, 156] succeeded in degradation of cross-linked ethylene-vinyl acetate copolymers used in the production of sport shoes. This operation was achieved on grinded industrial wastes in suspension in CC14. In a second... [Pg.69]

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. [Pg.169]

Ethylene Copolymers. Ethylene copolymers probably are the most important materials in hot-melt formulations. Ethylene-vinyl acetate and ethylene-ethyl acrylate polymers are very versatile and available in a wide range of grades offering different co-monomer contents and viscosities. The melts are stable and compatible with various modifying resins, waxes, extenders, and fillers. Adhesion to many substrates is good—including the polyolefin plastics, which are difficult to bond with most other types of adhesive unless the surfaces are pre-treated. [Pg.98]

A new approach was proposed for making effective helmets which could replace the former British army steel helmet. Essentially the new helmet used modified phenolic resins reinforced with nylon, and the crown cap inside was thermoformed from polyethylene. Formerly the crown cap was attached to the steel by rivets—not an appropriate method for fixing polyethylene to reinforced plastics. Instead a method was developed with a hot-melt adhesive based on ethylene-vinyl acetate copolymers cast as film on release paper. For assembly, the cast film is cut in advance to match the intricate shape required and activated by heat to bond under light pressure subsequently, a further heat activation is employed to fix the crown cap in place (Figure 52 illustrates this). [Pg.111]

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. [Pg.54]

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,... [Pg.405]

Ethylene/vinyl Acetate Copolymers (EVA). LDPE is easily internally plasticized by copolymerization with increasing amounts (2-20%) of vinyl acetate comonomer. [Pg.643]


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See also in sourсe #XX -- [ Pg.227 , Pg.361 , Pg.386 , Pg.394 , Pg.897 ]

See also in sourсe #XX -- [ Pg.227 , Pg.361 , Pg.386 , Pg.394 , Pg.897 ]

See also in sourсe #XX -- [ Pg.227 , Pg.361 , Pg.386 , Pg.394 , Pg.897 ]




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