Surfaces, TPEs studies

Fluoroelastomers Novikova et al. [32] reported unproved physico-mechanical properties of fluoro mbbers by reinforcement with chopped polyamide fibers. Other fiber reinforcements are covered by Grinblat et al. [33]. Watson and Francis [34] described the use of aramid (Kevlar) as short fiber reinforcement for vulcanized fluoroelastomer along with polychloroprene mbber and a co-polyester TPE in terms of improvement in the wear properties of the composites. Rubber diaphragms, made up of fluorosilicone mbbers, can be reinforced using aramid fiber in order to impart better mechanical properties to the composite, though surface modification of the fiber is needed to improve the adhesion between fluorosUicone mbber and the fiber [35]. Bhattacharya et al. [36] studied the crack growth resistance of fluoroelastomer vulcanizates filled with Kevlar fiber. 

Thomas and co-workers [1986] studied effects of gamma-irradiation on a thermoplastic elastomer, TPE, a polyether-ester block copolymer from 1,4-butanediol, polybutylene glycol and terephthalic acid (Hytrel D40), TPE, and its blends with PVC, in air, at doses of 1, 10, 100 and 500 kGy. Visual inspection of the samples showed no color change up to 500 kGy, but the samples irradiated at 500 kGy showed surface cracks. 

Although ATR has been used to quantify the variation in composition at the surface in TPEs (Sung and Hu, 1980), a related utility is its ability to monitor in situ processes such as reaction injection molding (RIM) (Ishida and Scott, 1986) and protein adsorption onto a polyurethane substrate (Pitt and Cooper, 1986). In the latter, the effect of shear rate on the kinetics of protein adsorption and desorption from phosphate-buffered saline (PBS) was studied in a specially designed flow cell. A very thin film of the commercial MDI-ED-PTMO polyurethane Biomer was cast from solution onto a Ge ATR prism. The thickness of the film was less than the penetration depth so the protein concentration could be monitored after the infrared absorption of the polymer... 

Another extremely important parameter of any surface technique is the depth of penetration (d ), which is a characteristic distance from the surface that the measurement will probe. Table V gives approximate depths of penetration for the methods discussed in this section for measurement of TPE surfaces. Since Table V shows that the depth of penetration varies widely, the change in composition can be monitored from the surface almost continuously to thousands of angstroms. Alternatively, some methods discussed in this section measure the morphology near the surface. Studies of TPE surfaces are less numerous than investigations of bulk properties, which in general speaks to the relative lack of importance of the surface properties of TPEs for most applications. However, exceptions to the latter generalization definitely exist, for example in the medical device area. 

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