Ethylene flame properties

Prepare a saturated solution of sodium sulphide, preferably from the fused technical sodium polysulphide, and saturate it with sulphur the sulphur content should approximate to that of sodium tetrasulphide. To 50 ml. of the saturated sodium tetrasulphide solution contained in a 500 ml. round-bottomed flask provided with a reflux condenser, add 12 -5 ml. of ethylene dichloride, followed by 1 g. of magnesium oxide to act as catalyst. Heat the mixture until the ethylene dichloride commences to reflux and remove the flame. An exothermic reaction sets in and small particles of Thiokol are formed at the interface between the tetrasulphide solution and the ethylene chloride these float to the surface, agglomerate, and then sink to the bottom of the flask. Decant the hquid, and wash the sohd several times with water. Remove the Thiokol with forceps or tongs and test its rubber-like properties (stretching, etc.). 

Flame-Retardant Resins. Flame-retardant resins are formulated to conform to fire safety specifications developed for constmction as well as marine and electrical appHcations. Resins produced from halogenated intermediates (Table 5) are usually processed at lower temperatures (180°C) to prevent excessive discoloration. Dibromoneopentyl glycol [3296-90-0] (DBNPG) also requires glass-lined equipment due to its corrosive nature. Tetrabromophthahc anhydride (TBPA) and chlorendic anhydride (8) are formulated with ethylene glycols to maximize fiame-retardant properties reaction cycle times are about 12 h. Resins are also produced commercially by the in situ bromination of polyester resins derived from tetrahydrophthahc anhydride... 

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. 

These comprise components A to C, the amount of component B being 5 to 50 pbw per 100 pbw of A (based on solid content) and the amount of C being 50 to 350 pbw per 100 pbw of A (based on solid content). A is an emulsion of ethylene-vinyl ester copolymer, which is composed of 5 to 35 wt.% of ethylene and 95 to 65 wt.% of vinyl ester, and has a Tg of -25 to -I-15C and a toluene-insoluble part of 30 wt.% or more. B is a thermal expansive hollow microbead and C is an inorganic filler. The emulsion has superior mechanical strength, crack resistance, water resistance, alkali resistance, blocking resistance, foaming property, embossing property and superior flame resistance and can be used for flameproof foam sheet for wallpaper. 

Dicylopentadiene Resins. Dicyclopentadiene (DCPD) can be used as a reactive component in polyester resins in two distinct reactions with maleic anhydride (7). The addition reaction of maleic anhydride in the presence of an equivalent of water produces a dicyclopentadiene acid maleate that can condense with ethylene or diethylene glycol to form low molecular weight, highly reactive resins. These resins, introduced commercially in 1980, have largely displaced 0 0-phthalic resins in marine applications because of beneficial shrinkage properties that reduce surface profile. The inherent low viscosity of these polymers also allows for the use of high levels of fillers, such as alumina trihydrate, to extend the resin-enhancing, flame-retardant properties for application in bathtub products (Table 4). 

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. 

The traditional halogen fire retardants used in styrenic copolymers are decabromodiphenyl ether and octabromodiphenyl ether, tetrabromobisphenol A, bis(tribromophenoxy) ethane, ethylene bis-tetrabromophthalimide, and chlorinated paraffins. Actually the octabromodiphenyl ether has been banned on precautionary principles, as will be explained below. The fire-retardant capabilities of the more effective halogen-containing compounds are in line with the quantity of halogen in the final polymer blend, with consideration for the use of synergists. Thus, the practical utility of these flame-retardant compounds (once the issue of degradation temperature is resolved) is often based on their ability to be blended into the polymer and to not substantially affect the physical properties of the polymers. 

Lv, J., Qie, L., and Qu, B., Controlled synthesis of magnesium hydroxide nanoparticles with different morphological structures and related properties in flame retardant ethylene-vinyl acetate blends, Nanotechnology, 15, 1576-1581, 2004. 

Hermansson et al. carried out extensive investigations on the fire-retardant behavior of ethylene-acrylate copolymer modified with chalk and silicone elastomer.30 32 They have shown that incorporation of a silicone elastomer (at 5wt.%) and chalk filler (at 30wt.%) can greatly improve the flame-retardant properties of ethylene butyl acrylate formulations. The results show that, compared to the pure polymer, an increase in the LOI from 18 to 30, and a decrease in the peak heat release rate (PHRR) from 1300 to 330kW/m2 were observed. 

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. 

Ethylene shows all the chemical properties of alkenes. It undergoes combustion, addition reactions and polymerization reactions. It burns with a bright yellow flame. 

Polyphosphates derived from 4,4 -dihydric phenols or 4,4 -isopropylidenebis-phenol, bis(2,6-dibromophenol) and having an active moiety like 154 impart flame retardant properties [ W]. Thermostable polyesters were prepared by addition of bis(2-hydroxyethyl)phosphate prior to the final step of the polycondensation of ethylene glycol with dimethyl terephthalate [205]. Zinc salt of polydithiophosphate obtained by reaction of phosphorus pentasulfide with 4-substituted anisole was tested as AO in lubricating oils and greases. 

Condensation monomers having the benzimidazolin-2-one ring system have found utility as modifiers in polyester synthesis. In particular, halogenated diols (73) and dicarboxylic acids (74) may be incorporated (78MI11100) into poly(ethylene terephthalate) or poly(butyl-ene terephthalate) at fairly low levels to impart flame retardancy. This can be accomplished without adverse effects upon other polymer properties. 

Applications Gas chromatography has limited applications to filled systems. It was used for characterization of the various degradation products of ethylene ethyl acrylate copolymer filled with calcium carbonate by GC-MS, " evaluation of ecotoxi-cological properties of materials containing flame retardants,"" and determination of carbon black content by pyrolysis gas chromatography." ... 

---