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Fire retardant thermal

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. [Pg.84]

The feasibility of using these elastomeric foams as fire retardant thermal insulation has been demonstrated by a Department of the Navy-National Bureau of Standards Test Program (54). [Pg.238]

Perez RM, Sandler JKW, Altstadt V, Hoffmann T, Pospiech D, Ciesielski M, Doling M. Effect of DOP-based compounds on fire retardancy, thermal stability, and mechanical properties of DGEBA cured with 4,4 -DDS. J. Mater. Sci. 2006 41 341-353. [Pg.415]

In addition to the chemical mechanisms of fire retardants, thermal or barrier-type mechanisms may be operative. Coatings may prevent oxygen from reaching the wood surface. Dilution of combustible gases by noncombustible gases and inhibition of flaming by free radicals can also be in effect. Therefore, fire retardancy of wood involves many complex reactions. The effectiveness of a particular fire retardant depends on the overall summation of these competitive and sequential reactions and the thermal and physical environment of the material. [Pg.569]

In general, when compared with the conventional polymer composites, polymer nanocomposites exhibit significant improvements in different properties at relatively much lower concentration of filler. The efficiency of various additives in polymer composites can be increased manyfold when dispersed in the nanoscale. This becomes more noteworthy when the additive is used to address any specific property of the final composite such as mechanical properties, conductivity, fire retardancy, thermal stability, etc. In case of polyolefin/LDH nanocomposites, similar improvements are also observed in many occasions. For example, the thermal properties of PE/LDH showed that even a small amount of LDH improves the thermal stability and onset decomposition temperature in comparison with the unfilled PE [22] its mechanical properties revealed increasing LDH concentration brought about steady increase in modulus and also a sharp decrease in the elongation at break [25]. While in this section, fire-retardant properties and electric properties of polyolefin/LDH nanocomposite were described in detail. [Pg.235]

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. [Pg.373]

The drawbacks of cellular materials include limited temperature of appHcations, poor flammabiUty characteristics without the addition of fire retardants, possible health ha2ards, uncertain dimensional stabiUty, thermal aging and degradation, friabiUty, and embrittlement due to the effects of uv light (3,6,15). [Pg.332]

Another problem occurs when some fire retardant formulations ate exposed to elevated temperatures (eg, when used as roof tmsses or as roof sheathing) thermal-induced strength reductions can occur in-service. The thermo-chemical factors were discussed by LeVan and Winandy (26), and a kinetic degrade model was developed (27). The treater should be consulted to obtain appropriate in-service modifications for specific fire retardant treatments. [Pg.327]

Solutions of these fire retardant formulations are impregnated into wood under fliU cell pressure treatment to obtain dry chemical retentions of 65 to 95 kg/m this type of treatment greatly reduces flame-spread and afterglow. These effects are the result of changed thermal decomposition reactions that favor production of carbon dioxide and water (vapor) as opposed to more flammable components (55). Char oxidation (glowing or smoldering) is also inhibited. [Pg.329]

Some of the chemicals mentioned above and others, such as chlorinated mbber or paraffin, antimony trioxide, calcium carbonate, calcium borate, pentaerythrithol, alumina trihydrate, titanium dioxide, and urea—melamine—formaldehyde resin, may be used to formulate fire retardant coatings. Many of these coatings are formulated in such a way that the films intumesce (expand) when exposed to fire, thus insulating the wood surface from further thermal exposure. Fire retardant coatings are mostly used for existing constmction. [Pg.329]

The compounds so formed have excellent thermal stability and are self-extinguishing and even completely fire-retardant. Their properties are given in Table 13.14. A few common types of insulators and supports are shown in Figure 13.31. [Pg.369]

Whilst rigid closed-cell polyurethanes are excellent thermal insulators they do suffer from a limited and often unsatisfactory level of fire resistance, even in the presence of phosphorus-containing and halogen-containing fire retardants. Considerable promise is now being shown by the polyisocyanurates, which are also based on isocyanate chemistry. [Pg.805]

Baneijee et al. reported a number of soluble poly-imido [134], polyazomethine [135], and polyazoxy phos-phonates [136] by the two phase polycondensation method with or without any phase transfer catalyst. Resulting polymers exhibit high thermal stability and fire retardancy. [Pg.46]

SFC-FID is widely used for the analysis of (nonvolatile) textile finish components. An application of SFC in fuel product analysis is the determination of lubricating oil additives, which consist of complex mixtures of compounds such as zinc dialkylthiophosphates, organic sulfur compounds (e.g. nonylphenyl sulfides), hindered phenols (e.g. 2,6-di-f-butyl-4-methylphenol), hindered amines (e.g. dioctyldiphenylamines) and surfactants (sulfonic acid salts). Classical TLC, SEC and LC analysis are not satisfactory here because of the complexity of such mixtures of compounds, while their lability precludes GC determination. Both cSFC and pSFC enable analysis of most of these chemical classes [305]. Rather few examples have been reported of thermally unstable compounds analysed by SFC an example of thermally labile polymer additives are fire retardants [360]. pSFC has been used for the separation of a mixture of methylvinylsilicones and peroxides (thermally labile analytes) [361]. [Pg.217]

The use of copolymers is essentially a new concept free from low-MW additives. However, a random copolymer, which includes additive functions in the chain, usually results in a relatively costly solution yet industrial examples have been reported (Borealis, Union Carbide). Locking a flame-retardant function into the polymer backbone prevents migration. Organophosphorous functionalities have been incorporated in polyamide backbones to modify thermal behaviour [56]. The materials have potential for use as fire-retardant materials and as high-MW fire-retardant additives for commercially available polymers. The current drive for incorporation of FR functionality within a given polymer, either by blending or copolymerisation, reduces the risk of evolution of toxic species within the smoke of burning materials [57]. Also, a UVA moiety has been introduced in the polymer backbone as one of the co-monomers (e.g. 2,4-dihydroxybenzophenone-formaldehyde resin, DHBF). [Pg.721]

Examples A, closed cell thermal insulation with high fire retardency and low smoke generation (52,54) B, pigmented APN coatings in aluminum substrates with low flammability, low flame spread, and low smoke (55) C, APN insulation and cable jacketing (56) D, open cell APN comfort cushioning (57). (Photograph courtesy of the Firestone Tire... [Pg.239]

Aluminium hydroxide is essentially non-toxic, but does require high addition levels to be effective. As a result, the physical properties of the compound usually suffer. Its fire retardancy action results from the endothermic reaction which releases water under fire conditions and produces a protective char . The endothermic reaction draws heat from the rubber/filler mass and thus reduces the thermal decomposition rate. The water release dilutes the available fuel supply, cooling the rubber surface and mass. [Pg.149]

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. [Pg.90]

No discussion of polymer fire retardance would be complete without at least a brief mention of the highly aromatic polymers, all of which are very difficultly flammable if they burn at all (1 ). Although the low flammability of phenolic and furane resins are well known, these thermally... [Pg.93]

L. Costa, G. Camino and L. Trossaarelli, "Thermal Degradation of Fire Retardant Chloroparaffin - Metal Compound Mixtures - Part I. Antimony Oxide,"Polym. Degradation and Stability, 5, 267 (1983). [Pg.128]

Mechanism of Thermal Degradation of Fire-Retardant Melamine Salts... [Pg.211]

The salts can be classified in three main classes salts which undergo thermal dissociation to acid and melamine salts of strong acids which catalyse melamine condensation salts of acids which react with melamine condensation products. Implications of the thermal behaviour of the salts in the mechanism of fire retardance is briefly discussed. [Pg.211]

Melamine and its salts are widely used in formulations of fire retardant additives, particularly of the intumescent type (4-71. The role played by melamine structures in these additives is however not yet understood. The thermal behaviour is of paramount importance in studies of the fire retardance mechanism. It is known that melamine undergoes progressive condensation on heating with elimination of ammonia and formation of polymeric products named "melam", "melem", "melon" (8.91. The following schematic reaction is reported in the literature (10-121 ... [Pg.211]


See other pages where Fire retardant thermal is mentioned: [Pg.151]    [Pg.151]    [Pg.314]    [Pg.452]    [Pg.532]    [Pg.338]    [Pg.344]    [Pg.327]    [Pg.111]    [Pg.463]    [Pg.593]    [Pg.129]    [Pg.140]    [Pg.950]    [Pg.345]    [Pg.574]    [Pg.434]    [Pg.91]    [Pg.93]    [Pg.95]    [Pg.204]    [Pg.213]   


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Fire retardance

Fire retardancy

Fire retardant polymers thermal properties

Fire retardant thermal insulation

Fire retardants, thermal decomposition

Fire retardants, thermal decomposition products

Fire retardents

Fire-retardant fillers thermal degradation

Fire-retardant fillers thermal effects

Fire-retarding

High Thermal-Resistant and Fire-Retardant Coatings

Thermal properties fire retardants

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