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Acrylonitrile-butadiene rubber particle size distribution

Fig. 35. Dependence of fracture energy on the modifier composition (CTBN 1300 X 9 = carboxyl-tenninated acrylonitrile, acrylic acid and butadiene rubber with 18% acrylonitrile and 2% acrylic acid contents CTBN 1300x 13 = carboxyl-terminated acrylonitrile, butadiene rubber with 26% acrylonitrile content) (Reprinted from Journal of Materials Science, 27, T.K. Chen, Y.H. Jan, Fracture mechanism of toughened epoxy resin with bimodal rubber-particle size distribution, 111-121, Copyright (1992), with kind permission from Chapman Hall, London, UK)... Fig. 35. Dependence of fracture energy on the modifier composition (CTBN 1300 X 9 = carboxyl-tenninated acrylonitrile, acrylic acid and butadiene rubber with 18% acrylonitrile and 2% acrylic acid contents CTBN 1300x 13 = carboxyl-terminated acrylonitrile, butadiene rubber with 26% acrylonitrile content) (Reprinted from Journal of Materials Science, 27, T.K. Chen, Y.H. Jan, Fracture mechanism of toughened epoxy resin with bimodal rubber-particle size distribution, 111-121, Copyright (1992), with kind permission from Chapman Hall, London, UK)...
FIGURE 38.9 Particle size distribution of ambient ground acrylonitrile butadiene rubber (NBR) waste powder. (Reprinted from Anandhan, S., De, P.P., Bhowmick, A.K., Bandyopadhyay, S., and De, S.K., J. Appl. Polym. Sci., 90, 2348, 2003. With permission from Wiley InterScience.)... [Pg.1059]

The morphology of ruber modified epoxy photopolymers was found to depend on the cure conditions as well as the nature and concentration of rubber. The commercially available acrylonitrile-butadiene copolymer rubber modifiers with varying percentages of acrylonitrile content were used. They were polymerized using a photocationic initiator involving a UV exposure followed by a thermal cure. Transmission electron micrographs of osmium tetroxide stained specimens, coupled with dynamic mechanical measurements indicated that phase separation and particle size distribution depended not only on rubber concentration and compatibility, but also on the cure conditions. [Pg.345]

Ishida et reported melt blending of PLA with four types of common rubbers, ethylene-propylene copolymer (EPM), ethylene-acrylic rubber (EAM), acrylonitrile-butadiene rubber (NBR) and isoprene rubber (IR), to toughen PLA. All blends showed separated phase morphology where the elastomer phase was homogeneously distributed in the form of small droplets in the continuous PLA phase. Izod impact testing showed that toughening was achieved only when PLA was blended with NBR, which showed the smallest rubber particle size in the blends. In addition, the interfacial tension between both phases, PLA and NBR, was the lowest. [Pg.202]

Toughening epoxy matrices using liquid reactive rubbers (such as carboxyl-terminated butadiene acrylonitrile, CTBN, or the amine-terminated equivalent, ATBN) has been widely reported in the literature. Spherical rubber particles of a proper size distribution (usually 1-5 pm) can effectively enhance the toughness through crack blunting or cavitation mechanisms. However, rubber modification of epoxies becomes... [Pg.400]


See other pages where Acrylonitrile-butadiene rubber particle size distribution is mentioned: [Pg.321]    [Pg.331]    [Pg.1058]    [Pg.38]    [Pg.122]    [Pg.92]    [Pg.106]    [Pg.21]    [Pg.2746]    [Pg.231]    [Pg.421]    [Pg.1045]    [Pg.1190]    [Pg.133]    [Pg.362]    [Pg.130]    [Pg.265]    [Pg.874]    [Pg.419]    [Pg.4]    [Pg.28]   
See also in sourсe #XX -- [ Pg.1059 ]




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