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Poly polyethylene blends

We have tested the following polymers polycarbonate (PC), poly-carbonate/4% polyethylene blend (PC/PE), poly (ethylene terephthal-ate) (PET), ABS, and impact modified polystyrene (HIPS). All materials except PC were compression molded into nominal Vs-inch sheets. The PC used was an Vs-inch extruded sheet heat-treated in a manner previously described (22). These PC specimens were considered to be... [Pg.107]

Doube, C. P. Walsh, D. J., "Studies of Poly(vinyl chloride)/Solution Chlorinated Polyethylene Blends by Inverse Gas Chromatography," Eur. [Pg.170]

As reported by Diehl et al. [58], interpolymers are also compatible with a broader range of polymers, including styrene block copolymers [59], poly(vinyl chloride) (PVC)-based polymers [60], poly(phenylene ethers) [61] and olefinic polymers such as ethylene-acrylic acid copolymer, ethylene-vinyl acetate copolymer and chlorinated polyethylene. Owing to their unique molecular structure, specific ESI have been demonstrated as effective blend compatibilizers for polystyrene-polyethylene blends [62,63]. The development of the miscibility/ compatibility behavior of ESI-ESI blends differing in styrene content will be highlighted below. [Pg.617]

Fig. 23. The relative surface tension difference -Ay/y(T) between components of six poly-olefinic blends grouped in three microstructurally identical pairs Xj/x2 (x1>x2) 66/52 (Q, ), 86/75 (A, ) and 75/66 (V, Y). Open and solid symbols correspond to blends with deu-terated more (x,) and less (x2) branched components, respectively. Large and small symbols correspond to previously determined whole segregation isotherms and singular surface excess data, respectively [16,120,145]. y(T) is given by Eq. (45) for polyethylene. Solid lines denote average values for each blend at Tref=100 °C (thick bar)... Fig. 23. The relative surface tension difference -Ay/y(T) between components of six poly-olefinic blends grouped in three microstructurally identical pairs Xj/x2 (x1>x2) 66/52 (Q, ), 86/75 (A, ) and 75/66 (V, Y). Open and solid symbols correspond to blends with deu-terated more (x,) and less (x2) branched components, respectively. Large and small symbols correspond to previously determined whole segregation isotherms and singular surface excess data, respectively [16,120,145]. y(T) is given by Eq. (45) for polyethylene. Solid lines denote average values for each blend at Tref=100 °C (thick bar)...
Benzene can be separated over cyclohexane with an revalue of 26 with a polvinyl alcohol-poly(allylamine) blend containing a cobalt(II) complex.213 An a-value of 60 has been obtained by pervaporation with a poly(acrylonitrile-co-methyl methacrylate) membrane.214 Membranes of porous polyethylene grafted with glycidyl methacrylate215 and poly(A,A-dimethylacrylamide-co-methyl methacrylate)216 have also been used in this separation with separation factors of 21-22. This is a separation that would be difficult to do by size and by distillation. The two boil only 2°C apart. The cyclohexane produced by the reduction of benzene is the starting material for nylon. The best solution to the problem is to run the reduction to 100% completion. [Pg.190]

Examples of such compatibilized systems that have been studied include EPDM/PMMA blends compatibilized with EPDM- -MMA, polypropylene/polyethylene blends with EPM or EPDM, polystyrene/nylon-6 blends with polystyrene/nylon-6 block copolymer, and poly(styrene-co-acrylonitrile)/poly(styrene-co-butadiene) blends with butadiene rubber/PMMA block copolymer. [Pg.534]

I. Kolesov, O. Dolynchuk, S. Borieck, H.-J. Radusch, Morphology-controlled multiple one-and two-way shape-memory behavior of cross-linked polyethylene/poly( -caprolactone) blends. Polym. Adv. Technol. doi 10.1002/pat.3338... [Pg.150]

Monika, P. Upadhyaya, N. Chand, Vi Kumar, Effect of poly lactic acid on morphological, mechanical, and optical properties of compatibilized polypropylene and high density polyethylene blend. Compos. Interfaces 21, 133-141 (2014)... [Pg.154]

Siddaramaiah, M.N. Satheesh Kumar, G.B. Nando, Rheological and mechanical properties of poly(ethylene acrylic acid) and low density polyethylene blends. J. Appl. Polym. Sci. 121, 3070-3077 (2011)... [Pg.155]

M. Kollar, G. Zsoldos, Investigating poly-(vinyl-chloride)-polyethylene blends by thermal methods. J. Therm. Anal. Calorim. 107, 645-650 (2012)... [Pg.156]

Fig. 4.120 Fatigue strength in flexural alternating range of two poly(vinyl chloride)/polyethylene-blends [98Dom]. Fig. 4.120 Fatigue strength in flexural alternating range of two poly(vinyl chloride)/polyethylene-blends [98Dom].
Fig. 4.189a Time to fracture as a function of applied stress intensity factor for poly(vinyl chloride) (a) and poly(vinyl chloride)/chlorinated polyethylene blend [95Bre]. Fig. 4.189a Time to fracture as a function of applied stress intensity factor for poly(vinyl chloride) (a) and poly(vinyl chloride)/chlorinated polyethylene blend [95Bre].
The use of mixtures of polymers where one of them acts as a compatibilizer between starch and less hydrophilic components e.g. PVA in TPS/polyethylene blends or a low molecular weight polymer like poly(ethylene glycol) in TPS/PLA blends [50, 110, 115, 119]). [Pg.333]

S. MaUick, A.K. Dhibar, B.B. Khatua, Effect of nanoclay on the morphology and properties of poly(methyl methacrylate)/high-density polyethylene blends. Journal of Applied Polymer Science 116 (2) (2010) 1010-1020. [Pg.49]

Wenig W. Meyer K. Investigation of the crystallization behaviour of polypropylene— polyethylene blends by optical microscopy. Kolloid-Zeitschrift Zeitschriftfiir Poly-mere. 1980,258(9), 1009-1014. [Pg.169]

Esso Research and Engineering Company, Improved Polypropylene-Polyethylene Blends, Br. Pat. 934,640 (1963). Physical or thermoplastic crystalline/crystalline IPNs. Poly-ethylene/polypropylene blends. Improved low-temperature properties. [Pg.247]

Stell J R, Paul D R and Barlow J W (1976) Mechanical properties of oriented polyethylene/poly-styrene blends, Polym Eng Sci 16 496-506. [Pg.434]

Li Z M, Yang W, Xie B H, Shen K Z, Huang R and Yang M B (2004) Morphology and tensile strength prediction of in situ microfibrillar poly(ethylene terephthalate)/polyethylene blends fabricated via slit-die extrusion- hot stretching-quenching, Macromol Mater Eng 289 349-354. [Pg.434]

Jiang C H, Zhong G J and Li Z M (2007) Recyclabihty of in situ microfibrillar poly(ethylene terephthalte)/high-density polyethylene blends, Macromol Mater Eng 292 362-372. [Pg.626]

The compositions of poly(ethylene-co- ropylene) were estimated from the A 25 /Aj absorbance ratios of the IR spectrumfwith a Bomem MB—102 Infrared Spectrophotometer). The calibration curve for the absorbcince ratios was obtained by using polypropylene—polyethylene blends dissolved in xylene. [Pg.266]

Jams, D Summers, J.W., Hiltner, A., and Baer, E. (2000) Weld line strength of poly (vinyl chloride)/polyethylene blends. Polymer, 41, 3057-3068. [Pg.296]

Figure 8.32 Melt flow index variation with blend composition for high-density poly-ethylene/low-density polyethylene blend at 190°C and 2.16-kg test load condition for MFI using data from Ref. 87 (validity at all temperatures). (Reprinted from Ref. 78 with kind permission from Steinkopff Verlag Darmstadt.)... Figure 8.32 Melt flow index variation with blend composition for high-density poly-ethylene/low-density polyethylene blend at 190°C and 2.16-kg test load condition for MFI using data from Ref. 87 (validity at all temperatures). (Reprinted from Ref. 78 with kind permission from Steinkopff Verlag Darmstadt.)...
The favorable effect on polyolefin miscibility of statistical segment length asymmetry due to the entropy contributions required for conformational adjustments has also been emphasized by Bates et al. [87]. In a series of papers. Bates and Fredrickson [88] attributed the miscibility of athermal or nearly athermal polymer mixtures mainly to these conformational asymmetries which contribute substantially to a nonlocal conformational excess entropy of mixing. The effect is exemplified for the amorphous polyethylene/poly-(ethylethylene) blend. Due to the fact that unperturbed PE and PEE molecules cannot be randomly interchanged, a positive excess free energy of mixing caused by nonlocal excess entropy contribution is anticipated by the authors. The effect of asymmetry on polymer miscibility is also supported by computer simulations, which suggest additional contributions due to entropy density differences of the pure polymeric phases [89]. [Pg.219]

Polyethylene blends with Poly(styrene-co-butadiene) Polycarbonate Nylon 6... [Pg.68]

Mechanical testing (strain-stress, tensile strength, elongation at break, elastic modulus, melt flow, viscoelastic properties, etc), have frequently been used in the study of the photodegradation of polyethylene [711, 1656, 1704, 1750, 1957, 2124, 2128], polypropylene [1750, 1899, 1903], poly(styrene) [748], poly(styrene-co-carbon monoxide) [1429], poly(styrene-co-acrylonitrile) [747], EPDM [896], poly(vinyl chloride) [806,1137,1138,1232,1748,1938], impact modified poly(vinyl chloride) [761, 764,1232], nylon 6 [672, 726, 727, 1395,1396,2300,2305], polyethylene blends with nylon 6 [506], and polyurethanes and its blends with poly(vinyl chloride), poly(vinyl alcohol), poly(vinyl acetate) and poly(vinyl chloride-co-vinyl acetate) [652]. [Pg.569]


See other pages where Poly polyethylene blends is mentioned: [Pg.96]    [Pg.46]    [Pg.587]    [Pg.134]    [Pg.19]    [Pg.217]    [Pg.76]    [Pg.160]    [Pg.203]    [Pg.16]    [Pg.17]    [Pg.266]    [Pg.222]    [Pg.216]    [Pg.246]    [Pg.2606]    [Pg.2791]    [Pg.6267]    [Pg.117]    [Pg.49]    [Pg.410]   


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