Mechanical properties polypropylene-vinyl acetate

Chattopadhyay S., Chaki T.K., and Bhowmick A.K., New thermoplastic elastomers from poly(ethyle-neoctene) (engage), poly(ethylene-vinyl acetate) and low-density polyethylene by electron beam technology structural characterization and mechanical properties. Rubber Chem. TechnoL, 74, 815, 2001. Roy Choudhury N. and Dutta N.K., Thermoplastic elastomeric natural rubber-polypropylene blends with reference to interaction between the components. Advances in Polymer Blends and Alloys Technology, Vol. 5 (K. Finlayson, ed.), Technomic Publishers, Pensylvania, 1994, 161. 

On mechanical rather than thermal properties, plastics which were harder were also more difficult to cut and to fabricate satisfactorily. Chemically, plastics which resisted organic solvents were also more difficult to print safely and with good results, and so forth. Often, in practice, intractable properties were modified to the required degree by the inclusion of small amounts of other monomers (vinyl acetate in vinyl chloride a-olefins in polypropylene, etc.)—just as an unwanted property like brittleness in polystyrene was ameliorated by adding to it styrene-butadiene. 

Thomas, S., Gupta, B. R., De, S. K., Mechanical properties, surface morphology and failure mode of gamma-ray irradiated blends of polypropylene and ethylene-vinyl acetate rubber. Polymer Degradation and Stability 1987,18(3), 189-212. 

The combination of HALS with a UV absorber is used in fihns of polypropylene and polyethylene as well as in thick sections. In films of LDPE, nickel quenchers were commonly used with a UV absorber, except in a very thin film, in which a higher concentration of nickel stabilizer is superior to the combination. The low-molecular-weight HALS are not sufficiently compatible with LDPE at the concentrations necessary, possibly as high as 2%, for the required protection. Incompatibility of HALS with LDPE has been overcome with the development of polymeric HALS. It is considerably better than either the UV absorber or nickel quencher or combinations of the two. For thicker films (100-200 ftm), the combination of a benzophenone-type UV absorber with polymeric HALS is significantly superior to an equivalent amount of polymeric HALS. The type of stabilizers used for linear low-density polyethylene (LLDPE) and ethyl vinyl acetate (EVA) copolymer are similar to those for LDPE. Since LLDPE has superior mechanical properties (elongation at break and tensile strength), thinner films can be used for most applications, and the loss of UV stabihty with reduction in thickness has to be compensated for by improving the stabilization system. 

Ethylene-vinyl acetate copolymers, usually known as EVA, are used in many applications, but especially for low voltage cables. These polymers are easily flammable and flame retardants are added to reduce their flammability. The classic solution is to incorporate aluminium hydroxide or magnesium hydroxide that develop endothermic reactions when heated. Nevertheless, large amounts have to be incorporated, often around 60% and this can lead to a loss of mechanical properties in the compound. Intumescent technology that works well with polypropylene has also been tried for EVA polymer systems. 

Thermoplastics used to blend with NR include PS, " polyamide 6, ethylene-vinyl acetate (EVA) copolymer, poly(methyl methacrylate) (PMMA), polypropylene (PP), low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE) " and high-density polyethylene (HDPE). To improve the properties of TPNR, modified NR is also used. ENR is the most frequently used modified NR. TPNR blends are prepared by blending NR and thermoplastics in various proportions. The role of rubber is to improve the impact strength and ductility of the plastic. Depending on the ratio, materials with a wide range of properties are obtained. The stiffness of the rubber is increased with the incorporation of plastic into the rubber matrix. The mechanical properties of TPNR again depend on the proportions of the rubber and thermoplastic components. The elastic properties of TPNR are considerably... 

Until 2003, Chen s [28], Qu s [29-31], and Hu s [32] groups independently reported nanocomposites with polymeric matrices for the first time the. In Hsueh and Chen s work, exfoUated polyimide/LDH was prepared by in situ polymerization of a mixture of aminobenzoate-modified Mg-Al LDH and polyamic acid (polyimide precursor) in N,N-dimethylactamide [28]. In other work, Chen and Qu successfully synthesized exfoliated polyethylene-g-maleic anhydride (PE-g-MA)/LDH nanocomposites by refluxing in a nonpolar xylene solution of PE-g-MA [29,30]. Then, Li et al. prepared polyfmethyl methacrylate) (PMMA)/MgAl LDH by exfoliation/adsorption with acetone as cosolvent [32]. Since then, polymer/LDH nanocomposites have attracted extensive interest. The wide variety of polymers used for nanocomposite preparation include polyethylene (PE) [29, 30, 33 9], polystyrene (PS) [48, 50-58], poly(propylene carbonate) [59], poly(3-hydroxybutyrate) [60-62], poly(vinyl chloride) [63], syndiotactic polystyrene [64], polyurethane [65], poly[(3-hydroxybutyrate)-co-(3-hydroxyvalerate)] [66], polypropylene (PP) [48, 67-70], nylon 6 [9,71,72], ethylene vinyl acetate copolymer (EVA) [73-77], poly(L-lactide) [78], poly(ethylene terephthalate) [79, 80], poly(caprolactone) [81], poly(p-dioxanone) [82], poly(vinyl alcohol) [83], PMMA [32,47, 48, 57, 84-93], poly(2-hydroxyethyl methacrylate) [94], poly(styrene-co-methyl methacrylate) [95], polyimide [28], and epoxy [96-98]. These nanocomposites often exhibit enhanced mechanical, thermal, optical, and electrical properties and flame retardancy. Among them, the thermal properties and flame retardancy are the most interesting and will be discussed in the following sections. 

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]. 

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