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Cross-over molecular mass

Styrene Copolymer Dispersions. The and hardness of polystyrene can be adjusted over a wide temperature range by copolymerization of styrene with soft monomers such as butadiene and acrylate esters. Styrene-butadiene (SB) dispersions are quantitatively the most important. With a styrene-butadiene weight ratio of 85 15 the is ca. 80 C, at a ratio of 45 55 the T, is ca. — 25 C. On account of the cross-linking capability of butadiene, SB copolymers are not thermoplastics, but elastomers. Elasticity can be modified by controlling the molecular mass and degree of cross-linking. [Pg.35]

In vulcanized rubber the molecular chains are cross linked by chemical bonds which inhibit macro-flow. That is why vulcanized stocks are more perfectly elastic than raw rubber (cf. the models having piston and spring in series.) The chemical cross links, randomly distributed over the mass of rubber, act as permanent junction points. A netlike structure is obviously present in vulcanized rubber. [Pg.630]

As in a melt, the reptation time depends strongly on the molecular mass and, for high molecular mass polymers, can be as long as several seconds. As the concentration is decreased, the reptation time decreases and crosses over towards the Zimm time (the characteristic time of a dilute solution) at the overlap concentration c = c. ... [Pg.227]

Using trouser tear tests, Gent and Tobias [21] showed that the Lake-Thomas model held reasonably well for a number of elastomers. In their analysis, they took the molecular mass of a strand as that extracted from the elastic modulus and thereby incorporated the effect of entanglements (Section 9.8.2). More recent results on poly(dimethyl siloxane) (PDMS) elastomers using simple shear tests [22,23] over a wide range of structure (extent of cross-links and trapped entanglements) indicate that the role of entanglements in elastomer fracture needs to be elucidated further. [Pg.434]

A number of excellent reviews and books have included consideration of the fundamental electron impact ionization process, and the attention afforded the experimental measurement of ionization potentials and Augment ion appearance energies over the years is reflected in the comprehensive database of ionization potentials and gas phase ion enthalpies of formation published through the National Bureau of Standards in printed and electronic forms. In contrast, few absolute ionization cross sections have been measured. The most comprehensive compilation of molecular ionization cross sections are relative values measmed with a modified commercial electron impact mass spectrometer ion source using the cross section for Ar as a reference. ... [Pg.27]


See other pages where Cross-over molecular mass is mentioned: [Pg.14]    [Pg.14]    [Pg.14]    [Pg.15]    [Pg.14]    [Pg.14]    [Pg.14]    [Pg.15]    [Pg.259]    [Pg.89]    [Pg.48]    [Pg.363]    [Pg.336]    [Pg.4]    [Pg.413]    [Pg.136]    [Pg.373]    [Pg.561]    [Pg.286]    [Pg.190]    [Pg.96]    [Pg.200]    [Pg.254]    [Pg.253]    [Pg.5111]    [Pg.672]    [Pg.269]    [Pg.36]    [Pg.82]    [Pg.17]    [Pg.465]    [Pg.125]    [Pg.872]    [Pg.564]    [Pg.44]    [Pg.157]    [Pg.224]    [Pg.280]    [Pg.40]    [Pg.243]    [Pg.403]    [Pg.90]    [Pg.2]    [Pg.277]    [Pg.382]    [Pg.214]    [Pg.133]   
See also in sourсe #XX -- [ Pg.11 , Pg.12 , Pg.13 ]




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Cross over

Crossing-over

Molecular mass

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