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Chemical oxidative degradation poly ethylene oxide

Two reactions can occur during wear oxidative degradation as a result of frictional heating in the contact zone and mechanochemical degradation initiated by shear-induced rupture of chemical bonds. Present evidence favors the latter process. For example, in the absence of oxygen, the wear of cis-polyisoprene changes to resemble that of c/x-polybutadiene, whereas the wear of poly(ethylene-co-propylene) is unaltered (Gent and Pulford, 1983). These results are in accord with the response of these materials to free radical reactions. [Pg.512]

Polymers are widely used as implant materials because they have physical properties that are similar to those of natural tissues. Examples are long-term and shortterm implants such as blood vessels, heart valves, membranes, mesh prostheses, corneas, tracheal prostheses, dental materials, parts of the nose and ear, knee and hip joints, and others. The synthetic polymers used include polyethylene (PE), particularly ultrahigh molecular weight PE (UHMWPE), poly(ethylene terephthal-ate) (PET), poly(tetrafluoroethylene) (PTFE), polyurethane (PU), and poly(methyl methacrylate) (PMMA). The necessary sterilization before implantation can be performed by y-irradiation, heat (steam), or chemical treatment (ethylene oxide), which should not cause any structural degradation of the polymers. Current challenges in research include the development of biomimetic materials that match both the mechanical and biological properties of their natural counterparts. [Pg.488]

Rubbers, often based on poly diene rubbers or else copolymers of dienes like 1,3-butadiene, were the first successful toughening additives, and they are effective partly because they have a low modulus, 100 to 500 times lower than that of most thermoplastic polymers. Unfortunately polydienes introduce chemical double bonds which are susceptible to UV, thermal and oxidative degradation. Hydrogenation removes some of them. Acrylic compounds and ethylene copolymers are also popular impact modifiers, and they do not necessarily introduce double bonds. [Pg.66]


See other pages where Chemical oxidative degradation poly ethylene oxide is mentioned: [Pg.488]    [Pg.208]    [Pg.246]    [Pg.1816]    [Pg.13]    [Pg.129]    [Pg.247]    [Pg.789]    [Pg.13]    [Pg.11]    [Pg.400]    [Pg.474]    [Pg.154]    [Pg.331]    [Pg.227]    [Pg.347]    [Pg.169]    [Pg.1113]    [Pg.299]    [Pg.81]    [Pg.215]    [Pg.160]    [Pg.259]    [Pg.1297]    [Pg.522]    [Pg.426]    [Pg.210]    [Pg.374]   
See also in sourсe #XX -- [ Pg.141 , Pg.142 , Pg.145 ]




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Chemical degradation

Chemical oxidants

Chemical oxidation

Chemical oxidizers

Chemicals oxidizing

Degraded poly

OXIDATION OXIDATIVE DEGRADATION

Oxidations degradative oxidation

Oxidative degradation

Oxidized Poly

Poly , oxidative

Poly chemical oxidation

Poly oxidative degradation

Poly oxide

Poly(ethylene

Poly(ethylene oxide

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