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Polyolefins crystalline

Crosslinking reduces the polyolefin crystallinity. Crosslinks play the role of defect centres which impede the folding of macromolecules and thus decrease the sizes of the lamellar crystals. Even a small number of crosslinks reduces the crystallinity of low density polyethylene provided that it is performed above the melting tonperature of the polymer crystallites. The linkage of polymer chains impedes their independoit displacement and the degree of crystallinity is distinctly Iowa even when only one macromolecule involves one crosslink [160]. [Pg.186]

Tg was measured by gas-chromatography in the following polyolefines crystalline-amorphous polypropylene [1], isotactic, atactic and syn-diotactic polypropylene [170], polyethylene of various densities, polyiso-butene and poly(l-butene) [130], polybutadiene [206]. [Pg.170]

Polyolefins. In these thermoplastic elastomers the hard component is a crystalline polyolefin, such as polyethylene or polypropylene, and the soft portion is composed of ethylene-propylene rubber. Attractive forces between the rubber and resin phases serve as labile cross-links. Some contain a chemically cross-linked rubber phase that imparts a higher degree of elasticity. [Pg.1024]

Because of the high melt viscosity of polyolefins, normal spinning melt temperatures are 240—310°C, which is 80—150°C above the crystalline melting point. Because of the high melt temperatures used for polyolefin fiber spinning, thermal stabilizers such as substituted hindered phenols are added. In the presence of pigments, the melt temperature must be carefully controlled to prevent color degradation and to obtain uniform color dispersion. [Pg.317]

Above 100°C, most polyolefins dissolve in various aHphatic and aromatic hydrocarbons and their halogenated derivatives. For example, polybutene dissolves in benzene, toluene, decalin, tetralin, chloroform, and chlorobenzenes. As with other polyolefins, solubiHty of PB depends on temperature, molecular weight, and crystallinity. [Pg.426]

Physical Properties. Table 3 Hsts physical properties of stereoregular polymers of several higher a-olefins. Crystal ceU parameters of these polymers ate available (34—36). AU. stereoregular polyolefins have helix conformations ia the crystalline state. Their densities usually range from 0.90 to 0.95 g/cm. Crystalline PMP, however, represents an exception its density is only 0.812—0.815 g/cm, lower even than that of amorphous PMP (0.835—0.840 g/cm ), thus making it one of the lowest densities among plastics. [Pg.427]

Polymorphism. Many crystalline polyolefins, particularly polymers of a-olefins with linear alkyl groups, can exist in several polymorphic modifications. The type of polymorph depends on crystallisa tion conditions. Isotactic PB can exist in five crystal forms form I (twinned hexagonal), form II (tetragonal), form III (orthorhombic), form P (untwinned hexagonal), and form IP (37—39). The crystal stmctures and thermal parameters of the first three forms are given in Table 3. Form II is formed when a PB resin crystallises from the melt. Over time, it is spontaneously transformed into the thermodynamically stable form I at room temperature, the transition takes about one week to complete. Forms P, IP, and III of PB are rare they can be formed when the polymer crystallises from solution at low temperature or under pressure (38). Syndiotactic PB exists in two crystalline forms, I and II (35). Form I comes into shape during crystallisation from the melt (very slow process) and form II is produced by stretching form-1 crystalline specimens (35). [Pg.427]

The minimum service temperature is determined primarily by the Tg of the soft phase component. Thus the SBS materials ctm be used down towards the Tg of the polybutadiene phase, approaching -100°C. Where polyethers have been used as the soft phase in polyurethane, polyamide or polyester, the soft phase Tg is about -60°C, whilst the polyester polyurethanes will typically be limited to a minimum temperature of about 0°C. The thermoplastic polyolefin rubbers, using ethylene-propylene materials for the soft phase, have similar minimum temperatures to the polyether-based polymers. Such minimum temperatures can also be affected by the presence of plasticisers, including mineral oils, and by resins if these become incorporated into the soft phase. It should, perhaps, be added that if the polymer component of the soft phase was crystallisable, then the higher would also affect the minimum service temperature, this depending on the level of crystallinity. [Pg.876]

Brosse et al. [41] modified isotactic polypropylene and other polyolefins by a cold plasma. In isotactic polypropylene, plasma treatment results in a polypropylene crystallization of paracrystalline or smectic form into a a-crystalline form. Further, the active films are susceptible to react with monomers in a postgrafting reaction. [Pg.527]

Other polyolefins A variety of other crystalline polyolefins are available such as polybutene-1 (improved creep resistance over polyethylene), poly-4-methyl pentene-1 (excellent temperature deformation resistance) and ethylene-vinyl acetate (greater flexibility). [Pg.933]

The operating pressures and shear rates in the extrusion process are considerably lower than they are in molding. As it exits the die, but not necessarily when it leaves the process, the material is in an essentially stress-free condition. Depending on the wall thickness of the material and the particular material, there is orientation of the plastic to a greater or lesser controllable degree. Thin walls produce higher orientation in materials such as PP, that is a highly crystalline polyolefin, and which orients much more than materials such as PVC. [Pg.282]

Dow ABS Nylon 6/6 Polycarbonate Polyethylene, HDPE, LDPE, LLDPE, ULDPE Polypropylene HPPP, CPPP Polystyrene HIPS, GPPS, Recycled, Advanced Styrenic Resin SAN Polyurethane Elastomers Polyolefin Plastomer PC/ABS Crystalline Polymer ABS/TPU... [Pg.628]

Mechanical properties, such as elastic modulus and yield point, that depend on crystallinity per se are not seriously affected by low to moderate doses of ionizing radiation. On the other hand, those mechanical properties that are sensitive to interlamellar activity are most dramatically affected by the low to moderate radiation doses. This is seen in the ultimate tensile strength and elongation at failure of the polyolefins. It is also reflected in the large change in melt index between 0 and 18 Mrad, which indicates formation of cross-links that increase with increasing... [Pg.98]

Tobolosky suggestion of crystalline and amorphous polyolefin copolymers Commercial PU elastic fiber, DuPont Commercial PU TPEs lonomeric TPE, DuPont (Surlyn)... [Pg.103]

New family of TPV having heat and oil resistance based on ACM and polyamide Development of crystalline-amorphous block copolymers (Engage), mettalocene catalyzed TPEs, Polyolefin elastomer (POEs), application research on TPEs Protein-based block-copolymer... [Pg.104]


See other pages where Polyolefins crystalline is mentioned: [Pg.45]    [Pg.44]    [Pg.5]    [Pg.1410]    [Pg.45]    [Pg.44]    [Pg.5]    [Pg.1410]    [Pg.313]    [Pg.313]    [Pg.317]    [Pg.331]    [Pg.426]    [Pg.426]    [Pg.426]    [Pg.427]    [Pg.428]    [Pg.430]    [Pg.515]    [Pg.148]    [Pg.469]    [Pg.95]    [Pg.485]    [Pg.17]    [Pg.175]    [Pg.271]    [Pg.359]    [Pg.461]    [Pg.563]    [Pg.716]    [Pg.69]    [Pg.112]    [Pg.428]    [Pg.97]    [Pg.98]    [Pg.99]    [Pg.597]    [Pg.114]   
See also in sourсe #XX -- [ Pg.328 ]




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Polyolefin crystallinity, crosslinking

Polyolefin crystallinity/morphology

Polyolefin semi-crystalline

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