Fire-retardant fillers types

In this chapter, an overview is presented of the principal fire-retardant filler types, including details of their origin, characteristics, and application. Consideration will then be given to their mechanism of action both as flame retardants and as smoke suppressants, and to means for potentially increasing their efficiency using synergists and nanoscale variants. 

Using this concept, it has been shown by cone calorimetry that over a 3 min combustion period, 3 and 6 mm thick laminated structures, made with different fire-retardant skin and unfilled core combinations can give similar resistance to ignition and comparable HRR and smoke extinction area (SEA) results to fully fire-retardant compositions (Table 7.4). Mechanical properties, in particular impact strength, were also found to be greatly enhanced by this approach, since less fire-retardant filler is present in the material. Whereas this approach has been demonstrated to be effective with hydrated fillers, it is applicable to all fire-retardant types. 

They also observed that carbon retention and subsequent oxidation could be very important and was particularly noticeable with magnesium hydroxide in polypropylene leading to a sharp exotherm of the type already illustrated in Figure 6.11. They also claimed that this could lead to greater heat feedback in the oxygen index test, thus reducing fire retardant filler effects. 

The carbon black generated by a fire from a rubber source increases the smoke density other products are highly toxic and often corrosive. The halogens, phosphates, borates, and their acids evolved during a fire corrode metals and electrical and electronic equipment. Hence many of the fire retardants described below cannot be used in situations where the toxic gases evolved will create their own hazards. In these cases inorganic hydroxides are used, at filler-type addition levels. Aluminium hydroxide and magnesium hydroxide are used as non-toxic fire retardant systems. 

Several micron-sized layered silicates, such as talcs, can improve the fire retarding behavior of EVA by partial substitution of metal hydroxides. Clerc et al.63 have shown that better fire performance was achieved using higher values of the lamellarity index and specific surface area for four different types of talcs in MH/EVA blends. Expanded mineral and charred layers were formed, similar to intumescent compositions with APP, proving the barrier effect on mass transfer, even at the micron scale for the mineral filler. 

Electrical and electronic devices are made utilizing several various types of plastic materials, thus when discarded their waste is difficult to recycle. The plastics employed in housing and other appliances are more or less homogeneous materials (among others PP, PVC, PS, HIPS, ABS, SAN, Nylon 6,6, the pyrolysis liquids of which have been discussed above). However, metals are embedded in printed circuit boards, switches, junctions and insulated wires, moreover these parts contain fire retardants in addition to support and filler materials. Pyrolysis is a suitable way to remove plastics smoothly from embedded metals in electrical and electronic waste (EEW), in addition the thermal decomposition products of the plastics may serve as feedstock or fuel. PVC, PBT, Nylon 6,6, polycarbonate (PC), polyphenylene ether (PPO), epoxy and phenolic resins occur in these metal-containing parts of EEW. 

Flame-retardants are used as additives in the preparation of fire retardant paints. They are decomposed by heat to produce nonflammable components, which are able to blanket the flames. Both inorganic and organic types of flame-retardants are available in the market. The most widely used inorganic flame-retardants are aluminum trihydroxide, magnesium hydroxide, boric acid, and their derivatives. These substances have a flame-retardant action mainly because of their endothermic decomposition reaction and their dilution effect. The disadvantage of these solids is that they are effective in very high filler loads (normally above 60 percent). 

Oil industry cables are usually finished with an extruded heavy-duty polymeric sheath such as PVC, PE or CSP. For situations where resistance to heat, oil and flames is necessary it is the practice to use special elastomerics that are identified as HOFR types. These compounds include EVA, EMA, CPE, and EPR together with suitable fillers that are used during their curing processes. BS7655 details the requirements for HOFR cables, and IEC60332 for their fire retardance. 

Intrinsically fillers can be divided into two types, reactive and inert. Reactive fillers will react with their environment. A good example of this is gibbsite (aluminium hydroxide), which will react with both acidic and basic substances. Aluminium hydroxide also loses its water of crystallisation at around 200 °C and this enables it to provide fire retardancy in polymer formulations. The silicate minerals (kaolin, mica, talc, quartz, etc.), are, in classical chemical terms, virtually inert, only being attacked by very strong acids and alkalis. The carbonate minerals and the hydroxide minerals are very reactive to acids. 

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