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PP/EVA blend

The cross-linking of a polymer could be enhanced by the incorporation of a second polymer easily cross-linkable. In PP/EVA blends containing 70% of PP and 30% of EVA, EVA was described to cross-link under low doses of irradiation, whereas PP underwent chain scissions. Minkova et al. found that higher amounts of EVA in PP matrix favored cross-linking and increased the cross-linking density. EVA in PP slows the oxidation of alkyl radicals of PP. °... [Pg.283]

Mihailova, M., Kresteva, M., Aivazova, N., Krestev, V, Nedkov, E., X-ray investigation of polypropylene and poly(ethylene-co-vinyl acetate) blends irradiated with fast electrons WAXS investigation of irradiated i-PP/EVA blends. Radiation Physics and Chemistry 1999, 56(5-6), 581-589. [Pg.299]

Aghjeh R. Masoud, Khonakdar A. Hossein, and Seyed H. Jafari. Application of mean-field theory in PP/EVA blends by focnsing on dynamic mechanical properties in correlation with miscibility analysis. Compos. B. Eng. 79 (2015) 74—82. [Pg.187]

The water sorption isotherms of all PP/EVA blends are shown in Figure 14.4. With regards to the EVA content, differences in water uptake are apparent... [Pg.428]

Figure 23.21 Growth of peroxyl radicals during copolymers of vinyl acetate content 18% and storage of PP and PP/EVA blends e-beam- 28%, respectively. Reprinted with permission irradiated with a dose of 25 kCy. PPE1(13) and from Ref [92] 2007, Elsevier. Figure 23.21 Growth of peroxyl radicals during copolymers of vinyl acetate content 18% and storage of PP and PP/EVA blends e-beam- 28%, respectively. Reprinted with permission irradiated with a dose of 25 kCy. PPE1(13) and from Ref [92] 2007, Elsevier.
In the PP/EVA blend system, the effect of mixing time (converted as residence time) on phase coarsening has revealed a substantial linear particle size increase as a function of the mean residence time. As illustrated in Figure 22.4, the phase morphology is set up very fast (within a minute) and starts evolving by a more dominant coalescence process as the residence time is increased. The particle size is doubled after 2 min 30 s of residence time in the extruder. The pronounced coarsening effect is ascribed to a decrease in the viscosity of the dispersed phase a low viscosity favors flow of particles, their subsequent collision, and merging. [Pg.424]

Canto LB. On the coarsening of phase morphology of PP/EVA blends during compounding in a twin screw extruder. Polym Test 2014 34 175-182. [Pg.436]

Id. Thus, it is expected that in the modified PRP-EVA blend, probably due to interface modification by reactive processing, a transesterification between the pendant MAH group in MAH-PP, and acetate groups in the EVA elastomer, as predicted in reaction Scheme 1, the dispersed rubber particles become more efficient in craze initiation. [Pg.480]

It was proposed [85] that PLA could improve the properties of PP/HDPE/EVA blends. The mechanical properties showed that the polymer blend had optimum tensile and burst strengths at 4 wt% PLA incorporated into the PP/HDPE/EVA blend. The tear strength decreased with increasing PLA content in both the machine and the transverse directions. The friction coefficient was found to be the lowest at 4 wt% PLA... [Pg.138]

Dalai, S., Wenxiu, G., Radiation effects on poly(propylene) (PP)/ethylene-vinyl acetate copolymer (EVA) blends. Journal of Applied Polymer Science 2002, 86, 3420-3424. [Pg.299]

The double reptation model was used to evaluate viscoelastic behavior of metallocene-catalyzed polyethylene and low-density polyethylene blends by Peon et al. (2003). They compared their results with those obtained for HDPE/BPE blends prepared under similar conditions. Since this model assumes miscibility between the mixed species, the experimental viscosity of HDPE/BPE blends showed only small deviation compared to that expected according to the reputation miscible model. However, the model underestimated the compositional dependence of the zero-shear viscosity for mPE/LDPE blends, especially at intermediate levels. The enhanced zero-shear viscosity in immiscible blends such as PETG/EVA, PP/EVA, or EVA/PE blends was found to be more abrupt than it is for mPE/LDPE blends (Lacroix et al. 1996, 1997 Peon et al. 2003). [Pg.784]

Aliphatic dicarboxylic acid dichlorides were applied to the surface-saponified blend of 50 wt% poly(ethylene-co-propene) and 50 wt% poly(ethylene-co-vinyl acetate) (PP/EVA). After coupling without cyclization, the second carboxylic acid group is available for the covalent binding of the protein via the W-terminal amino group [ 140]. The use of anhydrides, e.g. glutaric acid anhydride, is another possibility to introduce free carboxyl groups into the polymer surface. [Pg.38]

Lasagabaster, A., Jose Abad, M., Barral, L., Ares, A., and Bouza, R. (2009) Application of FTIR spectroscopy to determine transport properties and water-polymer interactions in polypropylene (PP)/poly (ethylene-co-vinyl alcohol) (EVA) blend films effect of poly(ethylene-co-vinyl alcohol) content and water activity. [Pg.452]

Abolhasani, M., Arefazar, A., and Mozdianfard, M. (2010) Effect of dispersed phase composition on morphological and mechanical properties of PET/EVA/PP ternary blends. J. Polym. Sci. Part B Polym. Phys., 48 (3), 251-259. [Pg.702]

Figure 224 Number-average (dn) and volume-average (dv) diameters of EVA droplets in the PP/EVA 80/20 blends compounded in a Co-TSE as a function of the mean residence time (f), showing the coarsening kinetics during compounding in the Co-TSE. Canto [27]. Reproduced with permission of Elsevier. Figure 224 Number-average (dn) and volume-average (dv) diameters of EVA droplets in the PP/EVA 80/20 blends compounded in a Co-TSE as a function of the mean residence time (f), showing the coarsening kinetics during compounding in the Co-TSE. Canto [27]. Reproduced with permission of Elsevier.
EM micrographs of PP/EVA/silica blends. All the components were added simultaneously in the extruder, (a) PP/EVA2803 (/W =53,500g/mol)/hydrophilic silica, (b) PP/EVA28420 (W = 12,000g/mol)/hydrophilic silica, (c) PP/EVA2803/hydrophobic silica, (d) PP/EVA28420/hydrophobic silica [73]. [Pg.225]


See other pages where PP/EVA blend is mentioned: [Pg.277]    [Pg.26]    [Pg.314]    [Pg.700]    [Pg.386]    [Pg.430]    [Pg.118]    [Pg.223]    [Pg.277]    [Pg.26]    [Pg.314]    [Pg.700]    [Pg.386]    [Pg.430]    [Pg.118]    [Pg.223]    [Pg.473]    [Pg.479]    [Pg.511]    [Pg.47]    [Pg.50]    [Pg.41]    [Pg.139]    [Pg.113]    [Pg.1525]    [Pg.1526]    [Pg.1534]    [Pg.1537]    [Pg.1540]    [Pg.580]    [Pg.429]    [Pg.702]    [Pg.848]    [Pg.97]    [Pg.116]    [Pg.132]    [Pg.211]    [Pg.345]    [Pg.335]    [Pg.221]    [Pg.224]   
See also in sourсe #XX -- [ Pg.130 , Pg.428 ]




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PET Blends (with EVA, PE, PP, PA)

PP blends

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