Propylene flame properties

Acrylonitrile—Butadiene—Styrene. ABS is an important commercial polymer, with numerous apphcations. In the late 1950s, ABS was produced by emulsion grafting of styrene-acrylonitrile copolymers onto polybutadiene latex particles. This method continues to be the basis for a considerable volume of ABS manufacture. More recently, ABS has also been produced by continuous mass and mass-suspension processes (237). The various products may be mechanically blended for optimizing properties and cost. Brittle SAN, toughened by SAN-grafted ethylene—propylene and acrylate mbbets, is used in outdoor apphcations. Flame retardancy of ABS is improved by chlorinated PE and other flame-retarding additives (237). 

Chemical pretreatments with amines, silanes, or addition of dispersants improve physical disaggregation of CNTs and help in better dispersion of the same in rubber matrices. Natural rubber (NR), ethylene-propylene-diene-methylene rubber, butyl rubber, EVA, etc. have been used as the rubber matrices so far. The resultant nanocomposites exhibit superiority in mechanical, thermal, flame retardancy, and processibility. George et al. [26] studied the effect of functionalized and unfunctionalized MWNT on various properties of high vinyl acetate (50 wt%) containing EVA-MWNT composites. Figure 4.5 displays the TEM image of functionalized nanombe-reinforced EVA nanocomposite. 

Aryloxyphosphazene copolymers can also confer fireproof properties to flammable materials when blended. Dieck [591] have used the copolymers III, and IV containing small amounts of reactive unsaturated groups to prepare blends with compatible organic polymers crosslinkable by the same mechanism which crosslinks the polyphosphazene, e.g. ethylene-propylene and butadiene-acrylonitrile copolymers, poly(vinyl chloride), unsaturated urethane rubber. These blends were used to prepare foams exhibiting excellent fire retardance and producing low smoke levels or no smoke when heated in an open flame. Oxygen index values of 27-56 were obtained. 

Examples of fluoroplastics include polytetrafluoroethylene (PTFE), fluorinated ethylene propylene (FEP), ethylene—chlorotrifluoroethylene (ECTFE), ethylene—tetrafluoroethylene (ETFE), poly(vinylidene fluoride) (PVDF), etc (see Fluorine compounds, organic). These polymers have outstanding electrical properties, such as low power loss and dielectric constant, coupled with very good flame resistance and low smoke emission during fire. Therefore, in spite of their relatively high price, they are used extensively in telecommunication wires, especially for production of plenum cables. Plenum areas provide a convenient, economical way to run electrical wires and cables and to interconnect them throughout nonresidential buildings (14). Development of special flame-retardant low smoke compounds, some based on PVC, have provided lower cost competition to the fluoroplastics for indoors application such as plenum cable, Riser Cables, etc. 

Wang, Z., Shen, X., Fan, W., Hu, Y., Qu, B., andZou, G., Effects of poly(ethylene-co-propylene) elastomer on mechanical properties and combustion behaviour of flame retarded polyethylene/magnesium hydroxide composites, Polym. Int., 2002, 51(7), 653-657. 

Properties Colorless to pale yel. liq., fruity odor misc. with alcohol, fixed oils si. sol. in propylene glycol insol. in water m.w. 158.27 dens. 0.851-0.857 b.p. 150 C flash pt. 58 C ref. index 1.407 Toxicology LD50 (oral, rat) 8200 mg/kg, (skin, rabbit) > 5 g/kg low toxicity by ing. and skin contact skin irritant TSCA listed Precaution Flamm. when exposed to heat, flames, sparks, oxidizers Hazardous Decomp. Prods. Heated to decomp, emits acrid smoke and fumes NFPA Health 0... 

Definition Obtained by esterification of isovaleric acid with ethyl alcohol in presence of cone. H2SO4 Empirical C7H14O2 Formula (CH3)2CHCH2COOC2H5 Properties Colorless oily liq., apple odor sol. in propylene glycol si. sol. in water 135 C misc. with alcohol, fixed oils, benzene, ether m.w. 130.21 dens. 0.868 (20/20 C) b.p. 135 C m.p. -99 C flash pt. 77 F ref. index 1.395-1.399 Toxicology LD50 (oral, rabbit) 7031 mg/kg, (IP, rat) 1200 mg/kg mod. toxic by IP route mildly toxic by ing. skin irritant TSCA listed Precaution Flamm. liq. when exposed to heat, flame, or sparks... 

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. 

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