Polyethylene, considered

Even polyethylene specially treated for medical implants has aluminum as a contaminant ultrahigh molecular mass polyethylene, considered of special quality, may present up to 40 ppm A1 [77]. 

The polymer microstructure based on triad intensities in pyrolysates has been evaluated for poly(styrene-co-butyl acrylate), poly(styrene-co-methyl methacrylate), poly(vinyl chloride-co-vinylidene chloride), poly(styrene-co-maleic anhydride), and for chlorinated polyethylene considered as a copolymer of polyethylene and vinyl chloride [30]. 

The cos 4>j are not independent, but are tied together through trigonometric relationships. For an orthorhombic unit cell such as polyethylene, consider the... 

Chemically Resistant Fibers. Fibers with exceUent chemical resistance to corrosive and/or chemical warfare agents or extreme pH conditions (eg, very acidic or very alkaline) were initially used for protective clothing. However, appHcations for filtration of gases and Hquids in numerous industrial faciHties are now the more important. For example, PPS is suitable for use in filter fabrics for coal-fired boilers because of its outstanding chemical and heat resistance to acidic flue gases and its exceUent durabUity under these end use conditions. Many high tenacity fibers are also chemically inert or relatively unaffected under a variety of conditions. Aramids, gel spun polyethylene, polypropylene, fluorocarbon, and carbon fibers meet these criteria and have been used or are being considered for appHcations where chemical resistance is important. 

Carbon Cha.in Backbone Polymers. These polymers may be represented by (4) and considered derivatives of polyethylene, where n is the degree of polymeriza tion and R is (an alkyl group or) a functional group hydrogen (polyethylene), methyl (polypropylene), carboxyl (poly(acryhc acid)), chlorine (poly(vinyl chloride)), phenyl (polystyrene) hydroxyl (poly(vinyl alcohol)), ester (poly(vinyl acetate)), nitrile (polyacrylonitrile), vinyl (polybutadiene), etc. The functional groups and the molecular weight of the polymers, control thek properties which vary in hydrophobicity, solubiUty characteristics, glass-transition temperature, and crystallinity. 

Polyolefins such as polyethylene and polypropylene contain only C—C and C—H bonds and may be considered as high molecular weight paraffins. Like the simpler paraffins they are somewhat inert and their major chemical reaction is substitution, e.g. halogenation. In addition the branched polyethylenes and the higher polyolefins contain tertiary carbon atoms which are reactive sites for oxidation. Because of this it is necessary to add antioxidants to stabilise the polymers against oxidation Some polyolefins may be cross-linked by peroxides. 

At the time of writing photodegradants are in an early stage of development and have not yet been fully evaluated. It is a moot point whether or not manufacturers will put such materials into polymer compounds and thus increase the price about 5% without legal necessity. However, if such legislation, considered socially desirable by many, took place one might expect polyethylene... 

At the end of the 1970s considerable interest developed in what became known as linear low density polyethylenes (LLDPE) which are intermediate in properties and structure to the high pressure and low pressure materials. While strictly speaking these are copolymers it is most convenient to consider them alongside the homopolymers. The LLDPE materials were rapidly accepted by industry particularly in the manufacture of film. The very low density polyethylenes (VLDPE) introduced by Union Carbide in 1985 were closely related. 

In broad tonnage terms the injection moulding markets for high-density polyethylene and polypropylene are very similar. The main reasons for selecting polypropylene have been given above. In favour of HDPE is the inherently better oxidation and ultraviolet resistance. Whilst these properties may be greatly improved in polypropylene by the use of additives these may increase the cost of polypropylene compounds to beyond that which is considered economically attractive. It is for this reason that HDPE has retained a substantial part of the crate market. 

The linear low-density polyethylenes discussed in the previous chapter might be considered as variations of this type of polymer. 

A further class of ethylene-vinyl acetate copolymer exists where the vinyl acetate content is of the order of 3 mole %. These materials are best considered as a modification of low-density polyethylene, where the low-cost comonomer introduces additional irregularity into the structure, reducing crystallinity and increasing flexibility, softness and, in the case of film, surface gloss. They have extensive clearance as non-toxic materials. 

In addition to acting as impact modifiers a number of polymeric additives may be considered as processing aids. These have similar chemical constitutions to the impact modifiers and include ABS, MBS, chlorinated polyethylene, acrylate-methacrylate copolymers and EVA-PVC grafts. Such materials are more compatible with the PVC and are primarily included to ensure more uniform flow and hence improve surface finish. They may also increase gelation rates. In the case of the compatible MBS polymers they have the special function already mentioned of balancing the refractive indices of the continuous and disperse phases of impact-modified compound. 

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