Fire-retarding

Fire pictures Fire protection Fire-rated laminates Fire retardancy Fire retardant... 

Fire retardant treatments Fire-tube furnace Fireworks... 

Panels for siding might be cut to resemble rough-cut lumber and grooved at intervals to show the appearance of board-on-board siding. Other treatments might include pressure-treatment with preservatives or fire-retardant chemicals for special appHcations requiring these characteristics. 

A small amount of particleboard is made with a fire-retardant treatment for use in locations where codes require this material, as in some offices and elevators. Particleboards receive overlay and finishing treatments with ease. Wood veneers, melamine overlays, printed paper overlays, vinyl overlays, foils, and direct grain printing can all be done quite simply. A small amount of particleboard is also made in the form of shaped, molded articles such as furniture parts, paper roU plugs, bmsh bases, and even toilet seats. There is another small increment of particleboard made by the extmsion process. These products are made in small captive operations owned by furniture manufacturers which consume all of this production in their furniture. The extmsion process differs from conventional flat-pressed particleboard in that the wood furnish is forced between two stationary heated surfaces. The mats are formed from one edge and this edge is alternately formed and pushed between the heated platens, which are maintained at a distance equal to the thickness of board produced. This is an old, slow, small-scale process, but is stiU in use in at least one location. 

The reaction with sodium sulfite or bisulfite (5,11) to yield sodium-P-sulfopropionamide [19298-89-6] (C3H7N04S-Na) is very useful since it can be used as a scavenger for acrylamide monomer. The reaction proceeds very rapidly even at room temperature, and the product has low toxicity. Reactions with phosphines and phosphine oxides have been studied (12), and the products are potentially useful because of thek fire retardant properties. Reactions with sulfide and dithiocarbamates proceed readily but have no appHcations (5). However, the reaction with mercaptide ions has been used for analytical purposes (13)). Water reacts with the amide group (5) to form hydrolysis products, and other hydroxy compounds, such as alcohols and phenols, react readily to form ether compounds. Primary aUphatic alcohols are the most reactive and the reactions are compHcated by partial hydrolysis of the amide groups by any water present. 

With sheet or pipe, multilayer coextmsion can be used. SoHd outer-soHd core coextmsion can place an ABS grade on the outside that has special attributes such as color, dullness, chemical resistance, static dissipation, or fire-retardancy over a core ABS that is less expensive or even regtind. 

Production of pentaerythritol in the United States has been erratic. Demand decreased in 1975 because of an economic recession and grew only moderately to 1980 (69). The range of uses for pentaerythritol has grown rapidly in lubricants (qv), fire-retardant compositions, adhesives, and other formulations where the cross-linking capabiUties are of critical importance. 

Although the cross-sectional shape of the spinneret hole direcdy affects the cross-sectional shape of the fiber, the shapes are not identical. Round holes produce filaments with an approximately round cross section, but with crenelated edges triangular holes produce filaments in the form of a "Y." Different cross sections are responsible for a variety of properties, eg, hand, luster, or cover, in the finished fabric. Some fibers may contain chemical additives to provide light-fastness and impart fire retardancy. These are usually added to the acetate solution before spinning,... 

Film or sheet generally function as supports for other materials, as barriers or covers such as packaging, as insulation, or as materials of constmction. The uses depend on the unique combination of properties of the specific resins or plastic materials chosen. When multilayer films or sheets are made, the product properties can be varied to meet almost any need. Further modification of properties can be achieved by use of such additives or modifiers as plasticizers (qv), antistatic agents (qv), fire retardants, sHp agents, uv and thermal stabilizers, dyes (qv) or pigments (qv), and biodegradable activators. 

The assessment of the contribution of a product to the fire severity and the resulting hazard to people and property combines appropriate product flammabihty data, descriptions of the building and occupants, and computer software that includes the dynamics and chemistry of fires. This type of assessment offers benefits not available from stand-alone test methods quantitative appraisal of the incremental impact on fire safety of changes in a product appraisal of the use of a given material in a number of products and appraisal of the differing impacts of a product in different buildings and occupancies. One method, HAZARD I (11), has been used to determine that several commonly used fire-retardant—polymer systems reduced the overall fire hazard compared to similar nonfire retarded formulations (12). 

The materials of attention in promoting fire safety are generally organic polymers, both natural, such as wood (qv) and wool (qv), and synthetic, nylon (see Polyamides), vinyl, and mbber (qv). Less fire-prone products generally have either inherently more stable polymeric stmctures or fire-retardant additives. 

Useful materials incorporating fire-retardant additives are not always straightforward to produce. Loadings of 10% are common, and far higher levels of flame retardants are used in some formulations. These concentrations can have a negative effect on the properties and functions for which the materials were originally intended. Product-specific trade-offs are generally necessary between functionaUty, processibiUty, fire resistance, and cost. 

Another factor potentially affecting the market for halogenated fire retardants is the waste disposal of plastics (see Wastes, industrial). As landfiU availabihty declines or becomes less popular, two alternatives are incineration and recycling (qv). The nature of the combustion products from halogenated products requires carefiil constmction and maintenance of incinerators (qv) to avoid damage to the incinerator itself and a pubHc health problem from the exhaust. The ease of recycling used products also has a potential effect on fire retardants. 

Flame-retardant additives are capable of significant reduction in the ha2ard from unwanted fires, and techniques are now available to quantify these improvements. Combined with an understanding of fire-retardant mechanisms, polymer-retardant interactions, and reuse technology, formulations optimi2ed for pubHc benefit and manufacturing practicaUty can be selected. 

V. Babrauskas and R. D. Peacock, Proceedings of the Fire Retardant Chemicals Association (FRCA) Fall Meeting, Lancaster Pa., 1990, pp. 67—80. 

Reduction of Fire Hazard Using Fire Retardant Chemicals, Fire Retardant Chemicals Association, Lancaster, Pa., 1989. 

Handbook of Fire Retardant Coatings and Fire Testing Services, Technomic, Lancaster, Pa., 1990. 

TrialkylPhosphates. Triethyl phosphate [78-40-0] C H O P, is a colorless Hquid boiling at 209—218°C containing 17 wt % phosphoms. It may be manufactured from diethyl ether and phosphoms pentoxide via a metaphosphate intermediate (63,64). Triethyl phosphate has been used commercially as an additive for polyester laminates and in ceHulosics. In polyester resins, it functions as a viscosity depressant as weH as a flame retardant. The viscosity depressant effect of triethyl phosphate in polyester resins permits high loadings of alumina trihydrate, a fire-retardant smoke-suppressant filler (65,66). 

E. D. Weil and A. M. Aaronson, "Phosphoms Flame Retardants—Meeting New Requirements," iu Proceedings of the 1st European Conference on Flammability and Fire Retardants, Brussels, Belgium, July 1977, Technomic Publishing Co., Westport, Coim., 1978. 

Y. Uehara and Y. Ogawa, iu V. M. Bhatnagar, A., Advances in Fire Retardant Textiles, Prog. Eire Ret. Senes, Vol. 5, Technomic Publishing Co.,... 

The first known fire-retardant process found durable to laundering was developed in 1912 (4). A modification of an earlier process (5), this finish was based on the formation of a tin(IV) oxide [18282-10-5] deposit. Although the fabric resulting from treatment was flame resistant, afterglow was reputed to be a serious problem, resulting in the complete combustion of the treated material through smoldering. 

The weight and constmction of the fabric affect its burning rate and ease of ignition. Lightweight, loose-weave fabrics bum much faster than heavier weight fabrics therefore, a higher weight add-on of fire retardant is needed to impart adequate flame resistance. 

Coating Theory. This theory includes fire retardants which form an impervious skin on the fiber surface. This coating may be formed during normal chemical finishing, or subsequently when the fire retardant and substrate are heated. It excludes the air necessary for flame propagation and traps any tarry volatiles produced during pyrolysis of the substrate. Examples of this type of agent include the easily fusible salts such as carbonates or borates. 

The most extensive body of tests are provided under the auspices of ASTM Standard methods. Specific ASTM test designations and descriptions are available (48). The other compendium of fire-retardant tests are contained ia Federal Test Method Standards 191A (49). 

The Fire Tests for Flame Resistant Textiles and Films, issued by the National Fire Protection Association (NFPA) ia 1989, is the method most used by iadustrial fire-retardant finishers (ca 1993) (50). It has been approved by the American National Standards Institute. 

Finally, a modification has been carried out in which a polyacrylate emulsion is added to a normal tetrakis(hydroxymethyl)phosphonium sulfate [55566-30-8] (THPS), urea, and TMM fire-retardant treatment in an attempt to completely alleviate the strength loss during the finishing. Indeed, better retention of tensile properties is achieved with no loss in fire resistance (85). 

Ammonia—Gas-Cured Flame Retardants. The first flame-retardant process based on curing with ammonia gas, ie, THPC—amide—NH, consisted of padding cotton with a solution containing THPC, TMM, and urea. The fabric was dried and then cured with either gaseous ammonia or ammonium hydroxide (96). There was Httle or no reaction with cellulose. A very stable polymer was deposited in situ in the cellulose matrix. Because the fire-retardant finish did not actually react with the cellulose matrix, there was generally Httle loss in fabric strength. However, the finish was very effective and quite durable to laundering. 

THPOH—Ammonia—Tris Finish. By far the most effective finish for polyester—cotton textiles was a system based on the THPOH—NH treatment of the cotton component either foUowed or preceded by the appUcation of Tris finish to the polyester component. This combined treatment appeared to be effective on almost any polyester—cotton blend. A large amount of fabric treated in this way was sold throughout the United States and much of the rest of the world. Shortly after the introduction of Tris finishing, Tris was found to be a carcinogen. Most of the Tris treated production was in children s sleepwear, and this created a situation in which almost aU chemical fire-retardant-treated textiles were unfairly condemned as dangerous. Manufacturers mshed to replace chemically treated textiles with products produced from inherently flame-resistant fibers. Nowhere was the impact more severe than in the children s sleepwear market. New, safer materials have been introduced to replace Tris. Thus far none has been as completely effective. 

Cotton—Wool Blends. Although they command only a very small fraction of the cotton blend market, cotton—wool blends are easier to make fire resistant than cotton itself. As might be expected, twiU fabrics containing both cotton and wool had decreased burning rates and increased 01 values both before and after fire-retardant treatment (147). 

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