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Polyethylene with temperature

Fig. 6.4 The variation of the electriG strength of polyethylene with temperature. The inset diagram shows the type of recessed specimen used. Reproduced from Lawson (1966) with permission of the Institution of Electrical Engineers. Fig. 6.4 The variation of the electriG strength of polyethylene with temperature. The inset diagram shows the type of recessed specimen used. Reproduced from Lawson (1966) with permission of the Institution of Electrical Engineers.
Figure 5 shows the changes of these thermodynamic functions of polyethylene with temperature. [Pg.8434]

Fig. 6.6. Change of g-values for normal polyethylene with temperature O, A radical X, B-radical , meanscompletecoincidence of O and X (Ref,... Fig. 6.6. Change of g-values for normal polyethylene with temperature O, A radical X, B-radical , meanscompletecoincidence of O and X (Ref,...
Figure 5 Light transmission of polyethylene as a function of the curing agent concentration (plate thickness 1 mm, moulding temperature 160°C, time 15 min.). 1-noncured polyethylene 2, 3, and 4-quenched cured polyethylene with different concentrations of the curing agent 2-0.5%, 3-1%, 4-2%. Figure 5 Light transmission of polyethylene as a function of the curing agent concentration (plate thickness 1 mm, moulding temperature 160°C, time 15 min.). 1-noncured polyethylene 2, 3, and 4-quenched cured polyethylene with different concentrations of the curing agent 2-0.5%, 3-1%, 4-2%.
At 300°C and in the presence of KOH an increase in the molecular weight is observed, i.e., the reaction of macropolymerization is realized [38,39]. Potassium hydroxide is effectively inhibiting thermal destruction of polyethylene at temperatures from 350-375°C. The per cent change in molecular weight is half or one-third as high as that without the use of an inhibitor. At 400°C the efficiency of inhibition is insignificant. Potassium hydroxide with an ABC carrier is effective up to the temperature of 440°C due to the increased contact surface of the inhibitor with macroradicals. [Pg.84]

The effect of thermal aging on polyethylene and isotactic polypropylene have been studied by Konar et al. [49]. They used contact angle, contact angle hysteresis, and XPS to characterize the modified surfaces of the polymers. Hysteresis increased with aging temperature. In the case of polyethylene, thermal aging led to a significant increase in adhesion strength of polyethylene with aluminium, but the increase in the case of polypropylene was much less marked. [Pg.528]

The most common backbone structure found in commercial polymers is the saturated carbon-carbon structure. Polymers with saturated carbon-carbon backbones, such as polyethylene, polypropylene, polystyrene, polyvinyl chloride, and polyacrylates, are produced using chain-growth polymerizations. The saturated carbon-carbon backbone of polyethylene with no side groups is a relatively flexible polymer chain. The glass transition temperature is low at -20°C for high-density polyethylene. Side groups on the carbon-carbon backbone influence thermal transitions, solubility, and other polymer properties. [Pg.4]

Boothroyd et al. [74] recently determined the temperature dependence of the Kuhn length for polyethylene with the aid of small-angle neutron scattering. In the temperature range between 100 and 200°C, dlnC /dT = - 1.1 x 10 3 K 1... [Pg.56]

The properties are close to those of polyethylenes, with some differences due to the tertiary carbon linked to the backbone good mechanical properties at ambient temperature, low price, attractive price/property ratios, easy processing, chemical inertness, we absorption of water, low density, good electrical insulation even in wet media, feasibility of welding, versatility of processing methods, broad range of available melt flow rates (MFR). [Pg.243]

None of the experimental techniques described by Bonner, however, has been capable of providing reliable vapor-liquid equilibrium data at the combined extremes of elevated temperature and reduced pressure, conditions applicable to most commercial polymer-stripping operations. This problem has been addressed by Meyer and Blanks (1982), who developed a modified isopiestic technique that could be used when solubilities are low. Although the success of this new technique was demonstrated using just polyethylene with isobutane and propane, the idea shows considerable promise for obtaining data at unusual conditions of temperature and pressure. [Pg.67]

Polyethylene is an organic polymer with an amorphous crystalline structure, formed by the polymerization of ethylene gas. A low-density polyethylene with a processing temperature of 130 to 150°C has been evaluated in bench-scale and full-scale tests as a final waste form for evaporator concentrates, sludges, blowdown solutions, incinerator ash, and ion exchange resins. [Pg.551]


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Polyethylene temperature

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