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Polyethylene fusion

The use of steam is generally limited to polypropyleae and polyethylene fusion because impractical pressures are required to reach the temperature levels, eg, >200° C, required for bonding polyesters. In general, greater temperature control is required for area bonding polypropylene than for other polymers because the temperature difference between the matrix and biader fibers can be only 3°C (26). [Pg.168]

The use of steam is generally limited to polypropylene and polyethylene fusion because impractical pressures are required to reach the temperature levels... [Pg.5163]

Extrusion blow moulding of bottles has been successfully accomplished in reeent years by attention to the points mentioned above. It is to be noted here that UP VC has a much lower average specific heat between the proeessing temperature and room temperature than polyethylene and, being essentially amorphous, no latent heat of fusion. This leads to much less heat needing to be removed on cooling of mouldings and very short cycle times are possible. [Pg.350]

Other factors which can affect impact behaviour are fabrication defects such as internal voids, inclusions and additives such as pigments, all of which can cause stress concentrations within the material. In addition, internal welds caused by the fusion of partially cooled melt fronts usually turn out to be areas of weakness. The environment may also affect impact behaviour. Plastics exposed to sunlight and weathering for prolonged periods tend to become embrittled due to degradation. Alternatively if the plastic is in the vicinity of a fluid which attacks it, then the crack initiation energy may be reduced. Some plastics are affected by very simple fluids e.g. domestic heating oils act as plasticisers for polyethylene. The effect which water can have on the impact behaviour of nylon is also spectacular as illustrated in Fig. 2.80. [Pg.152]

It has also been inferred that differences found between crystallinities measured by density and those from heat of fusion by DSC area determination, as given for polyethylenes in the example of Figure 4 [72], may be related to baseline uncertainties, or not accounting for the temperature correction of AHc. Given that similar differences in crystallinity from density and heat of fusion were reported for isotactic poly(propylene) [43] and polyfaryl ether ether ketone ketone), PEEKK [73], other features of phase structure that deviate from the two-phase model may be involved in the crystallinity discrepancy. [Pg.262]

Fig. 5 Initial fold length L against undercooling AT = To - T for both melt- and solution-crystallized polyethylene, from different solvents [16]. Dashed line gives previous calculations (Model A [9], old model in Fig. 4), solid line shows the results from the new model in Fig. 4 after re-adjusting the energy of fusion per - CH2 - unit from E= 1.07 to E- 1.42 kcal/mol... Fig. 5 Initial fold length L against undercooling AT = To - T for both melt- and solution-crystallized polyethylene, from different solvents [16]. Dashed line gives previous calculations (Model A [9], old model in Fig. 4), solid line shows the results from the new model in Fig. 4 after re-adjusting the energy of fusion per - CH2 - unit from E= 1.07 to E- 1.42 kcal/mol...
Polyethylene terephthalate (9.94 mg) gave a peak of area 116.3 cm2 on melting on a DSC, whereas 5.89 mg of pure indium (AHtus = 28.45 J g 1) gave a peak of 40.0 cm2. Calculate the latent heat of fusion of this polyethylene terephthalate, and compare with the pure crystalline value AHtus = 117.57 J g. Comment on the answers. [Pg.501]

In 1904 Bally obtained a bluish violet solid by alkali fusion of benzanthrone at approximately 220 °C. Two isomeric compounds were isolated by vatting the reaction mixture and filtering off a sparingly soluble sodium salt. Oxidation of the filtrate gave a blue vat dye, violanthrone (6.75 Cl Vat Blue 20), as the main component. The less soluble residue similarly afforded a violet product, isoviolanthrone (6.76 Cl Vat Violet 10). The formation of isoviolanthrone can be suppressed by carrying out the fusion in a solvent such as naphthalene or a polyethylene glycol in the presence of sodium acetate and sodium nitrite. Dyes of this type are often referred to as dibenzanthrones. [Pg.302]

ISO 7214 1998 Cellular plastics - Polyethylene - Methods of test ISO 8085-1 2001 Polyethylene fittings for use with polyethylene pipes for the supply of gaseous fuels - Metric series - Specifications - Part 1 Fittings for socket fusion using heated tools (available in English only)... [Pg.235]

ISO/TR 11647 1996 Fusion compatibility of polyethylene (PE) pipes and fittings ISO 12176-1 1998 Plastics pipes and fittings - Equipment for fusion jointing polyethylene systems - Part 1 Butt fusion... [Pg.236]

Successful fusion (2) is a rare event, but the frequency can be improved by adding polyethylene glycol (PEG). To obtain only successfully fused cells, incubation is required for an extended period in a primary culture with HAT medium (3), which contains hypoxan-thine, aminopterin, and thymidine. Amino-pterin, an analogue of dihydrofolic acid, competitively inhibits dihydrofolate reductase and thus inhibits the synthesis of dTMP (see p. 402). As dTMP is essential for DNA synthesis, myeloma cells cannot survive in the presence of aminopterin. Although spleen cells are able to circumvent the inhibitory effect of aminopterin by using hypoxanthine and thymidine, they have a limited lifespan and die. Only hybridomas survive culture in HAT medium, because they possess both the immortality of the myeloma cells and the spleen cells metabolic side pathway. [Pg.304]

Figure 20 shows the phase diagram of polyethylene119). The existence range of the condis crystals increases with pressure and temperature. The enthalpy of the reasonably reversible, first order transition from the orthorhombic to the hexagonal condis phase of polyethylene is 3.71 kJ/mol at about 500 MPa pressure 121) which is about 80 % of the total heat of fusion. The entropy of disordering is 7.2 J/(K mol), which is more than the typical transition entropy of paraffins to their high temperature... [Pg.41]

Keywords Positron annihilation high density polyethylene interphase glass-filled silane coupling agent heat of fusion. [Pg.365]

The interfacial region modified by the silane has properties different from those of the bulk polyethylene. The crystallization in the interphase will be hindered due to the chemical bonds between the azidofunctional group and the polyethylene chains. Figure 6 shows this effect by a decrease of the heat of fusion (AH) with increasing number of silane layers for the composites with 20 and 50 vol% of glass. The AH values in Fig. 6 are in J/g polymer and were calculated from the values... [Pg.372]

Figure 6. Heat of fusion (A W). in J/g of the polymer matrix, of the silane-modified composites against the number of silane layers. The crystallinity scale on the right-hand side was obtained by assumine AH for a polyethylene crystal to be 290 J/g. Figure 6. Heat of fusion (A W). in J/g of the polymer matrix, of the silane-modified composites against the number of silane layers. The crystallinity scale on the right-hand side was obtained by assumine AH for a polyethylene crystal to be 290 J/g.
The fusion temperature of these polymers is low enough to allow the spinning of fibres and melt pressing of films 263). They can also be blended with normal thermoplastics such as polystyrene or polyethylene oxide)2711. The conductivity shows a percolation threshold of about 16% which is expected for a random distribution of conducting spheres. [Pg.32]


See other pages where Polyethylene fusion is mentioned: [Pg.704]    [Pg.704]    [Pg.168]    [Pg.979]    [Pg.73]    [Pg.263]    [Pg.184]    [Pg.448]    [Pg.596]    [Pg.596]    [Pg.574]    [Pg.574]    [Pg.427]    [Pg.262]    [Pg.264]    [Pg.265]    [Pg.636]    [Pg.150]    [Pg.44]    [Pg.194]    [Pg.182]    [Pg.235]    [Pg.236]    [Pg.237]    [Pg.88]    [Pg.143]    [Pg.96]    [Pg.164]    [Pg.31]    [Pg.46]    [Pg.374]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.239 ]




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