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Amorphous tensile strength

Polycarbonates are an unusual and extremely useful class of polymers. The vast majority of polycarbonates are based on bisphenol A [80-05-7] (BPA) and sold under the trade names Lexan (GE), Makrolon (Bayer), CaUbre (Dow), and Panlite (Idemitsu). BPA polycarbonates [25037-45-0] having glass-transition temperatures in the range of 145—155°C, are widely regarded for optical clarity and exceptional impact resistance and ductiUty at room temperature and below. Other properties, such as modulus, dielectric strength, or tensile strength are comparable to other amorphous thermoplastics at similar temperatures below their respective glass-transition temperatures, T. Whereas below their Ts most amorphous polymers are stiff and britde, polycarbonates retain their ductiUty. [Pg.278]

On the other hand, if an amorphous polymer is struck above the Tg, i.e. in the rubbery state, large extensions are possible before fracture occurs and, although the tensile strength will be much lower, the energy to break (viz. the area under the curve) will be much more, so that for many purposes the material will be regarded as tough. [Pg.190]

The type of counterion present in an ionomer may, or may not, have a significant effect of properties. For polyethylene-based ionomers, where the presence of crystallinity has an appreciable effect on properties, the type of counterion present does not appear to have a significant effect on either modulus or tensile strength, as Fig. 4 indicates. However, in amorphous ionomers, the effects of changing the counterion from a monovalent one, as in Na or K, to a divalent one, such as Ca, may be appreciable. [Pg.149]

Below Tg tensile strengths are usually at least as strong for crystalline polymers as for amorphous polymers. Between and T, the strength and rigidity will be very dependent on the degree of crystallinity and... [Pg.919]

Strength Fibrous minerals Ductility gaining tensile strength. Carbon fibers are more expensive fibrous minerals are least expensive but only slightly reinforcing. Reinforcement makes brittle resins tougher and embrittles tough resins. Fibrous minerals are not commonly used in amorphous resins. [Pg.350]

Deflection Temperature (HDT) Fibrous minerals Ductility yield much greater increases in HDT than do amorphous resins. As with tensile strength, fibrous minerals increase HDT only slightly. Fillers do not increase HDT. [Pg.350]

Amorphous -1-Can more than double —Lower tensile strength... [Pg.352]

Usually, crystallization of flexible-chain polymers from undeformed solutions and melts involves chain folding. Spherulite structures without a preferred orientation are generally formed. The structure of the sample as a whole is isotropic it is a system with a large number of folded-chain crystals distributed in an amorphous matrix and connected by a small number of tie chains (and an even smaller number of strained chains called loaded chains). In this case, the mechanical properties of polymer materials are determined by the small number of these ties and, hence, the tensile strength and elastic moduli of these polymers are not high. [Pg.211]

The new polymers are intermediate in composition and crystallinity between the essentially amorphous EPR and the semicrystalhne iPP. The presence of the complementary blocks of elastomers for both ethylene and propylene crystallinity should not indicate a similarity, beyond the levels of the crystallinity in the properties of the E-plastomers and the P-plastomers. The E-plastomers and the P-plastomers differ in their stmctural, rheological, as well as their thermal, mechanical, and elastic properties. In a comparison of the tensile strength and tensile recovery (tension set) from a 100% elongation for a range of P-plastomers and E-plastomers, the former have lower tension set than EPR and iPP. However, for comparative E-plastomers and P-plastomers at equivalent tensile strength, the latter have significantly better tension set. In summary, P-plastomers are tough polyolefins which are uniquely soft and elastic. [Pg.184]

Thermoplastic polymers can be heated and cooled reversibly with no change to their chemical structure. Thermosets are processed or cured by a chemical reaction which is irreversible they can be softened by heating but do not return to their uncured state. The polymer type will dictate whether the compound is completely amorphous or partly crystalline at the operating temperature, and its intrinsic resistance to chemicals, mechanical stress and electrical stress. Degradation of the basic polymer, and, in particular, rupture of the main polymer chain or backbone, is the principal cause of reduction of tensile strength. [Pg.21]


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See also in sourсe #XX -- [ Pg.97 , Pg.98 , Pg.108 , Pg.124 , Pg.134 , Pg.139 , Pg.148 , Pg.150 , Pg.214 ]




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