Thermoplastic retardant

Uses Solvent for organic materials, fats, phenol, camphor, dye extraction, perfumes, pharmaceuticals, thermoplastics retarding fermentation additive to dye and lacquer sol ns. organic synthesis medicine degreasing agent Regulatory SARA 313 reportable Manuf./Distrib. Aldrich http //www.sigma-aldrich.com... 

Ethylenebis(tetrabromophthalimide). The additive ethylenebis(tetrabromophthalimide) [41291 -34-3] is prepared from ethylenediamine and tetrabromophthabc anhydride [632-79-1]. It is a specialty product used ia a variety of appHcations. It is used ia engineering thermoplastics and polyolefins because of its thermal stabiUty and resistance to bloom (42). It is used ia styrenic resias because of its uv stabiUty (43). This flame retardant has been shown to be more effective on a contained bromine basis than other brominated flame retardants ia polyolefins (10). 

Cblorina.ted Pa.ra.ffins, The term chlotinated paraffins covers a variety of compositions. The prime variables are molecular weight of the starting paraffin and the chlorine content of the final product. Typical products contain from 12—24 carbons and from 40—70 wt % chlorine. Liquid chlotinated paraffins are used as plasticizers (qv) and flame retardants ia paint (qv) and PVC formulations. The soHd materials are used as additive flame retardants ia a variety of thermoplastics. In this use, they are combiaed with antimony oxide which acts as a synergist. Thermal stabilizers, such as those used ia PVC (see vinyl polymers), must be used to overcome the inherent thermal iastabiUty. 

R. Gachter and H. MuUer, eds. Plastics Additives Handbook, Hanser Pubhshers, Munich, Germany, 1987 H. Jenkner, "Flame Retardants for Thermoplastics, Chapt. 11 iu Gachter and Muder, pp. 535—564. 

Physical or chemical vapor-phase mechanisms may be reasonably hypothesized in cases where a phosphoms flame retardant is found to be effective in a noncharring polymer, and especially where the flame retardant or phosphoms-containing breakdown products are capable of being vaporized at the temperature of the pyrolyzing surface. In the engineering of thermoplastic Noryl (General Electric), which consists of a blend of a charrable poly(phenylene oxide) and a poorly charrable polystyrene, experimental evidence indicates that effective flame retardants such as triphenyl phosphate act in the vapor phase to suppress the flammabiUty of the polystyrene pyrolysis products (36). 

A series of compounded flame retardants, based on finely divided insoluble ammonium polyphosphate together with char-forming nitrogenous resins, has been developed for thermoplastics (52—58). These compounds are particularly useful as iatumescent flame-retardant additives for polyolefins, ethylene—vinyl acetate, and urethane elastomers (qv). The char-forming resin can be, for example, an ethyleneurea—formaldehyde condensation polymer, a hydroxyethylisocyanurate, or a piperazine—triazine resin. 

C2HgNg H4O2P2 (60). The pyrophosphate is reported to be only soluble to the extent of 0.09 g/100 mL water, whereas melamine orthophosphate is soluble to 0.35 g/mL. The pyrophosphate is the most thermally stable. Melamine orthophosphate is converted to the pyrophosphate with loss of water on heating. AH three are available as finely divided soflds. AH are used commercially in flame-retardant coatings (qv) and from patents also appear to have utihty in a wide variety of thermoplastics and thermosets. A detaHed study of the thermal decomposition of the these compounds has been pubHshed (61). 

Triphenyl phosphate [115-86-6] C gH O P, is a colorless soHd, mp 48—49°C, usually produced in the form of flakes or shipped in heated vessels as a hquid. An early appHcation was as a flame retardant for cellulose acetate safety film. It is also used in cellulose nitrate, various coatings, triacetate film and sheet, and rigid urethane foam. It has been used as a flame-retardant additive for engineering thermoplastics such as polyphenylene oxide—high impact polystyrene and ABS—polycarbonate blends. 

Usage of phosphoms-based flame retardants for 1994 in the United States has been projected to be 150 million (168). The largest volume use maybe in plasticized vinyl. Other use areas for phosphoms flame retardants are flexible urethane foams, polyester resins and other thermoset resins, adhesives, textiles, polycarbonate—ABS blends, and some other thermoplastics. Development efforts are well advanced to find appHcations for phosphoms flame retardants, especially ammonium polyphosphate combinations, in polyolefins, and red phosphoms in nylons. Interest is strong in finding phosphoms-based alternatives to those halogen-containing systems which have encountered environmental opposition, especially in Europe. 

E. Termine and K. G. Taylor, "A New Intumescent Flame Retardant Additive for Thermoplastics and Thermosets," n Additive Approaches to PolymerModification, SPE RETEC Conference Papers, Toronto, Ontario, Canada, Sept. 1989. 

Considerable effort is being made (ca 1993) to develop satisfactory flame retardants for blended fabrics. It has been feasible for a number of years to produce flame-resistant blended fabrics provided that they contain about 65% or more ceUulosic fibers. It appears probable that blends of even greater synthetic fiber content can be effectively made flame resistant. An alternative approach may be to first produce flame-resistant thermoplastic fibers by altering the chemical stmcture of the polymers. These flame-resistant fibers could then be blended with cotton or rayon and the blend treated with an appropriate flame retardant for the ceUulose, thereby producing a flame-resistant fabric. Several noteworthy finishes have been reported since the early 1970s. 

MixedPhosphona.te Esters. Unsaturated, mixed phosphonate esters have been prepared from monoesters of 1,4-cyclohexanedimethanol and unsaturated dicarboxyhc acids. Eor example, maleic anhydride reacts with this diol to form the maleate, which is treated with benzenephosphonic acid to yield an unsaturated product. These esters have been used as flame-retardant additives for thermoplastic and thermosetting resias (97). 

Ethylene vinyl acetate (EVA) polymers are used in thermoplastic and thermosetting jacketing compounds for apphcations that require flame retardancy combined with low smoke emission during the fire as well as the absence of halogen in the composition. 

Flame-Retardant Filler. Demand has increased for Mg(OH)2 as a nonhalogenated, flame-retardant filler for thermoplastics used in the aerospace, microelectronics, and cable and wire manufacturing industries (90). Producers of nonhalogenated, flame retardant fillers include Kyowa, Aluisuisse-Lonza (Magnifin product line), Morton, and a Dead Sea Periclase/Dead Sea Bromine joint venture (91). 

The binder system of a plastic encapsulant consists of an epoxy resin, a hardener or curing agent, and an accelerating catalyst system. The conversion of epoxies from the Hquid (thermoplastic) state to tough, hard, thermoset soHds is accompHshed by the addition of chemically active compounds known as curing agents. Flame retardants (qv), usually in the form of halogens, are added to the epoxy resin backbone because epoxy resins are inherently flammable. 

Noryl. Noryl engineering thermoplastics are polymer blends formed by melt-blending DMPPO and HIPS or other polymers such as nylon with proprietary stabilizers, flame retardants, impact modifiers, and other additives (69). Because the mbber characteristics that are required for optimum performance in DMPPO—polystyrene blends are not the same as for polystyrene alone, most of the HIPS that is used in DMPPO blends is designed specifically for this use (70). Noryl is produced as sheet and for vacuum forming, but by far the greatest use is in pellets for injection mol ding. 

Injection-Molded Products. Numerous housings, electrical enclosures, and cabinets are injection-molded from rigid PVC. These take advantage of PVC s outstanding UL flammabiUty ratings and easy mol ding into thin-waHed parts. PVC has developed melt flow capabiUties to the point where it competes with essentially any other flame-retarded engineering thermoplastic and molds easier than most. 

Polycarbonates. Polycarbonates (qv) are pardy crystalline thermoplastics with some disorder in the crystalline part and considerable order in the amorphous part. This disorder conveys high impact strength which, combined with its good transparency and outdoor exposure resistance, makes polycarbonates usefiil for vandal-resistant glazing and outdoor lighting. It is easily processed by extmsion and injection mol ding. Various uv and dame-retardant agents are often added. 

As with other so-called engineering thermoplastics, the polyacetals are available modified with glass fibre, and may contain fire retardants, and some grades are blended with PTFE. In 1982 Hoechst introduced blends of polyacetals... 

A manufacturer considering using a thermoplastic elastomer would probably first consider one of the thermoplastic polyolefin rubbers or TPOs, since these tend to have the lowest raw polymer price. These are mainly based on blends of polypropylene and an ethylene-propylene rubber (either EPM or EPDM) although some of the polypropylene may be replaeed by polyethylene. A wide range of blends are possible which may also contain some filler, oil and flame retardant in addition to the polymers. The blends are usually subject to dynamic vulcanisation as described in Section 11.9.1. 

Literatures are available on POSS-polymer composites synthesized from different thermoplastics [71-74]. These composites are lightweight and show good fire retardancy, thermal stability, and mechanical reinforcement. Literatures on POSS-rubber composites are yet to come in a big way. 

FIRE RETARDANT FILLERS. The next major fire retardant development resulted from the need for an acceptable fire retardant system for such new thermoplastics as polyethylene, polypropylene and nylon. The plasticizer approach of CP or the use of a reactive monomer were not applicable to these polymers because the crystallinity upon which their desirable properties were dependent were reduced or destroyed in the process of adding the fire retardant. Additionally, most halogen additives, such as CP, were thermally unstable at the high molding temperatures required. The introduction of inert fire retardant fillers in 1965 defined two novel approaches to fire retardant polymers. 

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