Читать книгу Non-halogenated Flame Retardant Handbook - Группа авторов - Страница 32

Red phosphorus is a polymeric form of elemental phosphorus consisting of non-periodic five- and six-membered rings with some crosslinks. Red phosphorus is made by prolonged heating of white phosphorus at about 250-300°C in anaerobic conditions. At the end of the production red phosphorus comes out in the form of cake like solid chunk which needs to be broken and milled. Being exposed to moist air, non-stabilized red phosphorus slowly reacts with water and oxygen producing phosphine and various phosphorous acids. Oxidation starts on the sharp edges which are considered to be active sites. Smaller dusty particles are the most susceptible to oxidation and because of this red phosphorus is usually sieved out to different fractions with the removal of dusty particles. In the late 80s a process of producing mostly spherical particles of red phosphorus [10] which are considered less prone to oxidation was developed in Japan. Red phosphorus is very thermally stable and environmentally benign [11] because being exposed to weathering conditions it eventually converts to phosphoric acids.

Red phosphorus is a controversial flame retardant because on one hand it is very efficient, allowing achievement of a V-0 rating in glass-filled polyamides or polyesters at only 6-12% wt. loading and on the other hand it is very combustible, and the powder can easily ignite if heated in the open air. This doesn’t create problems in molded plastics, but storage and processing of red phosphorus should be monitored very carefully. Because of possible accumulation of phosphine, the containers with red phosphorus should be opened under a fume hood or ventilation canopy. Direct compounding of red phosphorus requires an inert gas blanket to the extruder and all feeding equipment, which can be a very costly investment. Another disadvantage of red phosphorus is its red color which is difficult to overcome even with a high concentration of other colorants like TiO₂ [12, 13]. Because of this, red phosphorus containing molded parts are typically pigmented black [14].

Historically, red phosphorus was mostly used in Europe and Asia and almost not used in North America [15]. For safe handling, red phosphorus is usually coated, for example with urea-formaldehyde resin [16], and stabilized with metal oxides [17] or metal hydroxides[18] or metal salts [19] or hydrotalcite [20] which can react and scavenge the phosphine as it forms. In order to ensure safe handling red phosphorus is sold as a wet filter cake, or as a dispersion in an epoxy resin or as a dispersion in castor oil. Red phosphorus is also available in the form of masterbatches with a variety of polymers [21].

Red phosphorus is particularly useful in glass-filled polyamide 6.6 where a high processing temperature (> 280°C) excludes the use of less stable phosphorus compounds [11]. Many industrial studies have been done to find synergists for red phosphorus. It has been found helpful to combine red phosphorus with phenolic resins [22]. It is believed that under burning conditions, red phosphorus-phenolic combinations form a cross-linked network which eliminates flaming drips by reducing melt flow. A typical polyamide 6.6 formulation which contains 25 wt.% glass fibers, 7% wt. red phosphorus and 5% wt. phenolic resin gives a V-0 rating. It is interesting that polyethylene terephthalate (PET) is synergistic with red phosphorus when used in glass-filled polyamide 6.6 [23]. Recently synergistic combinations with other phosphorus flame retardants like hexaphenoxytricyclophosphazene [24] and aluminum phosphite were patented [25]. Combinations of red phosphorus, aluminum diethyl phosphinate and melamine salts also allow boosting the glow wire ignition temperature [26].

Early work on the flame-retardant mechanism of red phosphorus in polyamide 6 suggests a mostly gas phase mechanism of action due to depolymerization into white phosphorus and volatilization in the oxygen depleted atmosphere of the pre-flame zone [27]. Later Levchik et al. [28] studied thermal decomposition of polyamide 6 flame-retarded with red phosphorus in nitrogen and found that phosphate esters are formed even in an inert atmosphere. Similarly, it was found that interaction of red phosphorus with PET leads to the formation of phosphate esters [29]. A more recent study also confirms an increased solid residue of polyamide 6.6 in the presence of red phosphorus [30]. Although an interaction of red phosphorus with traces of O₂ and absorbed moisture [31] as well as H₂O formed during the thermal decomposition of the polyamide [32] is a possible explanation of the formation of phosphate esters, it is also possible that red phosphorus reacts directly with polyamide via a free radical mechanism as an electron spin resonance study suggests [28].

Despite the fact that red phosphorus is effective in both condensed and gas phase [33] it achieves V-0 rating only in nitrogen and oxygen containing heteropolymers, mostly engineering thermoplastics. In polyolefins, red phosphorus was found useful for a V-2 rating and a high limiting oxygen index (LOI) especially in polyethylene [34]. It is believed there is better match between the temperature of the thermal decomposition of polyethylene and the volatilization of red phosphorus compared to polypropylene [22]. It was shown that a V-2 rating at 1.6 mm could be obtained at a level as low as 2.5% finely divided red phosphorus (5 μm) [35]. Melamine-formaldehyde coating improves the efficiency of red phosphorus in polyolefins because it provides charring to enhance the flame-retardant effect of the phosphorus [36]. Although red phosphorus is not efficient alone in poly(acrylonitrile-butadiene-styrene) (ABS) it allows achievement of a V-0 rating at 8 wt. % loading when combined with 15 wt. % PET [37] or 8 wt. % magnesium hydroxide and 6 wt. % polyamide 6 [38].

Apart from thermoplastics red phosphorus finds applications in polyurethane foams, polyurethane elastomers [39], epoxy resins and textiles [40]. Typically, polyurethane foams are flame retarded with chloroalkyl phosphates, but in some applications where stringent fire tests are required red phosphorus can be used. For example, only 5 wt. % red phosphorus with 5 wt. % of melamine is required to pass the British BS 5852 Crib 5, furniture test [41] versus almost 20 wt. % of chloroalkyl phosphate combined with melamine. Red phosphorus combined with expandable graphite is used in automotive sound insulation foam under the hood [42].

In the mid 90s production of epoxy-molding compounds flame retarded by stabilized and coated red phosphorus for encapsulation of electronic devices started in Japan [43]. Because encapsulating epoxy is very heavily filled with silica only few percent of red phosphorus is enough to achieve a V-0 rating [44]. In the late 90s and early 2000s electronics manufacturers using red phosphorus containing molding epoxy started to receive massive recalls due to electronics failure. Further investigation showed that despite stabilization and coating, red phosphorus was still reacting with oxygen producing acids and phosphine which damaged semiconductor circuits [43]. In recent years more failures were reported in cables [45] and connectors [46] due to the presence of red phosphorus. Recently some electronics manufacturers announced a ban on red phosphorus in their products and resin manufacturers start reducing their red phosphorus-based lines of products. The only potential applications for red phosphorus in epoxy which are still being researched are light weight composites [47] and coatings [48].