Flame retardant polymeric composition

Abstract

The invention disclose halogen free thermoplastic or cross linked polymers compositions comprising a polyolefin and/or a polyolefin containing polar co-monomers and a combination of metal hydroxides and inorganic hypophosphite as a synergic, and optionally other ingredients. These compositions show a superior balance of flame retardant properties compared to already known corresponding halogen free formulations. Molded items obtained using the polymer composition according to the present invention are useful in a wide range of injection molding and extrusion applications, especially cables.

Claims

1. A thermoplastic or cross-linked polymer composition, comprising a thermoplastic or cross-linked polymer, wherein said thermoplastic or cross-linked polymer is selected from the group consisting of polyolefins, polar polyolefins, and their mixtures and said thermoplastic or cross-linked polymer composition includes a combination of at least a metal hypophosphite and a metal hydroxide, the combination having a ratio of the metal hypophosphite to the metal hydroxide within a range of 1:100 to 1:3 by weight.

2. The thermoplastic or cross-linked polymer composition according to claim 1, wherein said ratio is within a range of 1:70 to 1:5 by weight.

3. The thermoplastic or cross-linked polymer composition according to claim 1, wherein said ratio is within a range of 1:64 to 5:64 by weight.

4. The thermoplastic or cross-linked polymer composition according to claim 1, wherein the thermoplastic or cross-linked polymer composition further comprises additional ingredients and additives.

5. The thermoplastic or cross-linked polymer composition according to claim 4, wherein the thermoplastic or cross-linked polymer composition comprises a polymeric coupling agent.

6. The thermoplastic or cross-linked polymer composition according to claim 4, wherein the thermoplastic or cross-linked polymer composition comprises a copolymer with acrylic acid.

7. The thermoplastic or cross-linked polymer composition according to claim 4, wherein the thermoplastic or cross-linked polymer composition comprises a polymer grafted with maleic anhydride.

8. The thermoplastic or cross-linked polymer composition according to claim 4, wherein the thermoplastic or cross-linked polymer composition comprises a polydimethylsiloxane, silicone oil, or silicone gum.

9. The thermoplastic or cross-linked polymer composition according to claim 4, wherein the metal hypophosphite is uncoated.

10. The thermoplastic or cross-linked polymer composition according to claim 1, wherein said thermoplastic or cross-linked polymer is cross linked.

11. The thermoplastic or cross-linked polymer composition according to claim 1, wherein said metal hypophosphite is aluminum hypophosphite or calcium hypophosphite.

12. The thermoplastic or cross-linked polymer composition according to claim 1, wherein said thermoplastic or cross-linked polymer is selected from the group consisting of ethylene vinyl acetate (EVA), ethylene butyl acetate (EBA), ethylene methyl acrylate (EMA), and their mixtures.

13. The thermoplastic or cross-linked polymer composition according to claim 1, wherein said metal hydroxide is aluminum hydroxide or magnesium hydroxide.

14. The thermoplastic or cross-linked polymer composition according to claim 1, wherein the thermoplastic or cross-linked polymer composition comprises additional ingredients selected from the group consisting of magnesium hydroxide, calcium carbonate, aluminum hypophosphite, coupling agents, and polydimethylsiloxane.

15. The thermoplastic or cross-linked polymer composition according to claim 1, wherein the metal hypophosphite is uncoated.

16. The thermoplastic or cross-linked polymer composition according to claim 1, wherein the metal hypophosphite has a chemical formula: Me(H.sub.2PO.sub.2).sub.n in which n is an integer number ranging from 1 to 4.

17. The thermoplastic or cross-linked polymer composition according to claim 16, wherein the metal hypophosphite includes a metal of group I, II, III or IV of the periodic table of elements.

18. The thermoplastic or cross-linked polymer composition according to claim 1 used for tarpaulin, cable insulation or floor covering.

19. A thermoplastic polymer composition comprising a thermoplastic polymer, wherein said thermoplastic polymer is selected from the group consisting of polyolefins, polar polyolefins, and their mixtures and includes a combination of at least a metal hypophosphite and a metal hydroxide, the combination having a ratio of the metal hypophosphite to the metal hydroxide within the range of 1:100 to 1:3 by weight.

20. The thermoplastic polymer composition according to claim 19, wherein said thermoplastic polymer is a nonpolar polyolefin.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) The present invention relates to a polymer composition containing a flame retardant combination of an inorganic hypophosphite, a metal hydroxide, a polymer or polymer blends and optionally other additives as coupling agents, processing aids, fillers, crosslinking agents/co-agents, stabilizers and pigments.

(2) Inorganic Hypophosphites

(3) Hypophosphorus acid metal salts, also called inorganic phosphinates or inorganic hypophosphites (phosphorus valence state=+1) are known as effective halogen free flame retardant additives for polymers.

(4) Hypophosphites have the following chemical formula:
Me(H.sub.2PO.sub.2).sub.n
where: “n” is an integer number ranging from 1 to 4 in dependence of the valence of the metal Me. The metal is any atom belonging to the groups I, II, III and IV of the periodic table of the elements.

(5) Hypophosphite of sodium and calcium are widely commercially available and they are normally produced by reacting the corresponding metal hydroxide on yellow phosphorus, as for instance:
P.sub.4+2Ca(OH).sub.2+H.sub.2O.fwdarw.Ca(H.sub.2PO.sub.2).sub.2+CaHPO.sub.3+PH.sub.3

(6) Hypophosphite of metals other than calcium and sodium are normally produced through the hypophosphorus acid reaction on the metal hydroxide or by exchange reaction with the corresponding soluble metal salts (see for example “Hypophosphorus Acid and its salts”, Russian Chemical Review, 44 (12), 1975).

(7) The choice of hypophosphites is subjected to a number of critical factors. Particularly, suitable hypophosphites must be characterized by sufficient thermal stability to overcome melt processing at temperature higher than about 200° C. In case they do form hydrates they must be used in the corresponding anhydrous form and they must not be hygroscopic when successively exposed to ambient humidity. Examples of such hypophosphites are aluminum hypophosphite (CAS 7784-22-7), calcium hypophosphite (CAS 7789-79-9), manganese hypophosphite (10043-84-2), magnesium hypophosphite (CAS 10377-57-8), zinc hypophosphite (CAS 15060-64-7), barium hypophosphite (CAS 171258-64-3). Most preferred in the purpose of the present invention are aluminum and calcium hypophosphites.

(8) Aluminum hypophosphite, corresponding to chemical formula Al(H.sub.2PO.sub.2).sub.3, is currently produced by Italmatch Chemicals Spa (“Phoslite IP-A”) in a white powder form with a low humidity level, high purity and various PSD suitable for thermoplastic processing.

(9) Calcium hypophosphite, corresponding to chemical formula Ca(H.sub.2PO.sub.2).sub.2, is also currently produced by Italmatch Chemicals Spa (“Phoslite IP-C”).

(10) Aluminum and calcium hypophosphite, being flammable powders as most of anhydrous hypophosphites, are often commercialized as dry powders blended with other solid flame retardants agents, in masterbatch or in paste form, for making transport and manipulation operations easier.

(11) Thermoplastic polymers moulding materials containing hypophosphites as flame retardants have been described in the art.

(12) Polycarbonate containing hypophosphites as flame retardants have been described in WO 2005/044906. Polycarbonate is not in the purpose of the present invention.

(13) Polyamides containing hypophosphites as flame retardants have been described in WO 2005/075566. Polyamides are not in the purpose of the present invention.

(14) According to WO 2007/010318 polyolefin polymers, particularly polypropylene compositions, are made flame retardant by incorporating a synergic mixture of inorganic hypophosphite and halogenated organic compounds. Halogen compounds however do generate highly corrosive halogen based and other gases during combustion, and are becoming a topic of environmental concern, so olefin polymers compositions containing halogen are not in the object of the present invention.

(15) According to WO 2009/010812, a polymer compositions, particularly polyesters or polyamides, comprising hypophosphites coated with inorganic hydrates and/or organic salts, show good flame retardant performance but, at the same time, showed reduced polymer degradation compared to a corresponding polymer composition comprising uncoated hypophosphites. The claimed ratio hypophosphite to metal hydrate coating, is in the range 100/1 to 5/1 by weight. Such coated hypophosphites, when applied to polyolefins, polar polyolefins and crosslinked rubbers do not show satisfactory results in term of flame retardancy compared to existing formulations based on metal hydroxides. Increasing dramatically the metal hydroxide content in the system, so decreasing the ratio hypophosphite to metal hydroxide in the range from 5/1 to 1/3 by weight, flame retardancy became even worse.

(16) Surprisingly, according to the present invention, it has been discovered that when the amount of metal hypophosphite in the system is below the ratio: metal hypophosphite to metal hydroxide 1/3 by weight, flame retardancy is improved compared to existing metal hydroxide based formulations.

(17) Hypophosphites in the composition range according to the present invention are new flame retardant agents when used as synergic to metal hydroxides specifically on polyolefins and polar polyolefins.

(18) Metal Hydroxide

(19) Metal hydroxide, that can be also called metal hydrates, are flame retardant agents based on metal hydroxides salts or metal hydroxide molecules, able to release water upon heating, i.e. in the range from about 200° up to about 400° C. Examples are aluminum hydroxide and magnesium hydroxide, of both synthetic or natural origin and with different particle size and surface treatments. Other compounds are boehmite (aluminum oxide-hydroxide) or also layered double hydroxides, which may be referred as hydrotalcite. Mix of the different hydroxides with other fillers (not hydrate) like calcium carbonate or calcinated kaolin or natural occurring mineral silicates or magnesium carbonate or huntite or hydromagnesite are also in the scope of the present invention. Particularly, calcium carbonate is often employed to reduce cost and improve processing and mechanical properties of the compound.

(20) Polymer and Polymer Blends

(21) In the composition of the invention the polymer is at least a polyolefin, at least a polar polyolefin or a mixture of at least a polyolefin with at least a polar polyolefin. The term polyolefin is used for both olefin homo- or co-polymers. Example of polyolefins include homopolymers or copolymers of ethylene, propylene, butene, esene, isoprene, ottene. Possible polyolefins include: PP (Poly Propylene), LDPE (Low Density Poly Ethylene), LLDPE (Linear Low Density Poly Ethylene), VLDPE (Very Low Density Poly Ethylene), MDPE (Medium Density Poly Ethylene), HDPE (High Density Poly Ethylene), EPR (Ethylene Propylene Rubber), EPDM (Ethylene Propylene Diene Monomer) and Plastomers or Poly Olefin Elastomers like ethyelene 1-ottene or ethylene 1-esene produced with single site catalyst technology.

(22) The term polar polyolefins is used for copolymers of olefin with polar co-monomers, like vinyl acetate, alkyl acrylates, methacrylates, acryklic acids, methacrylic acid, acrylonitrile and styrene. Examples of polar polyolefins include EVA (Ethylene Vinyl Acetate), EVM (Ethylene Vinyl Monomer rubbers, the segment of EVA copolymers with vinyl acetate content between 40% and 90%), EBA (Ethylene Butyl Acrylate), EEA (Ethylene Ethyle Acrylate), EMA (Ethylene Methyl Acrylate), NBR (Nitrile Butadiene Rubber), SBR (Styrene Butadiene Rubber).

(23) It is particularly preferred, according to the present invention, that the polar polyolefin comprises a copolymer of ethylene with vinyl acetate with a vinyl acetate content from 4% to 80%, more preferably from 14% to 50%.

(24) Polar polyolefins, depending on their polar monomer content, confer good flame retardant properties, and may be used in combinations with polyolefins, conferring to the resulting polymer composition additional interesting properties such as good processability, better thermal resistance and electrical properties.

(25) Coupling Agents

(26) A polymeric coupling agent is a polymer that link an inorganic filler, for example Aluminum or Magnesium hydrate, to the polymer matrix. In any case the addition of high level of filler will reduce the elongation at break, and the toughness of the polymer. In order to overcome the drawbacks of the addition of fillers, coupling agents have to be added in order to reduce the repellency of the polymers and fillers respectively. As a result, the filler will adhere better to the polymer matrix and the properties of the final composite (mainly toughness and dispersion) will be enhanced. Because better filler dispersion may improve flame retardancy by avoid dripping and improving char consistency, coupling agents may also be considered as flame retardant coadjuvants. Maleated polymers are a well known family of functionalized polymers used as coupling agents. They can be prepared directly by polymerization or by modification during compounding (this process is called reactive extrusion). Silanes or aminosilanes are also used to improve adhesion between the filler and the polymer matrix. One example is vinyltrimethoxysilane.

(27) Processing Aids

(28) In the industrial field, the term “silicones” usually refer to linear or branched polydimehtylsiloxanes (PDMS) fluids and gums, used as a processing aid to improve extrusion, surface aspect, abrasion resistance, friction. They are also often used as flame retardant adjuvant. Silicones oil or gums are generally available in masterbatches form or supported on inert fillers with high surface area, like silica.

(29) Vinyl unsatured PDMS are also possible to be used in conjuction with radical initiators for in situ grafting into the polymer.

(30) According to the present invention, a particularly useful polymeric composition comprises aluminum or magnesium hydroxide, calcium carbonate, Aluminum hypophosphite, coupling agents and polydimethylsiloxane. This composition showed significant improvements when used in extrusion processes for cable insulation.

(31) The composition according to the invention is advantageously used in cable jacketing for low, medium or high voltage as well as for primary electrical insulation.

(32) Again, polymeric composition of the invention, is used for cable conduit extruded profile, roofing foil, molded pallet, tarpaulin, floor covering, wall covering.

(33) According to the present invention, polymer compositions, particularly polyolefin compositions, characterized by the presence of metal hydroxide or metal hypophosphite only as flame retardant agent, FIGRA values (in the first case i.e. metal hydroxide as sole flame retardant agent) and FPI values (in the second case i.e. metal hypophosphite as sole flame retardant agent) are not good enough to be considered as slightly satisfactory. When metal hydroxide concentrations raise with respect to the amount of metal hypophosphite, FIGRA and FPI values are not good as well. On the contrary, in case the ratio metal hydroxide/metal hypophosphite in the polymeric composition is 95/5 to 97/3 according to the present invention, surprisingly FIGRA and FPI values are optimal, particularly if compared with those deriving from the compositions according to the prior art.

(34) Particularly, it has been found that, according to the present invention, the following percentage range values of metal hypophosphite on the total weight % of the mixture metal hypophosphite+metal hydroxide are preferred: 1% to 33% 1% to 20% 1,5% to 9% 3% to 5%.
Experimental Part

(35) The lab-scale compounds were prepared in a 100 cc Brabender mixer at 180° C. with 60 rpm for 5 minutes. Compounds samples were pressed into 3 mm thick plaques at 180° C. for 5 minutes for subsequent cone calorimeter analysis. Each reported cone calorimeter measurement, is the mean of 5 single measurements performed at 35 kW/m2 irradiation in a Stanton Redcroft's machine. This kind of measurement calculates, through suitable software, the following parameters: TTI=Time To Ignition (kW/m2) HRR=Heat Release Rate (kW/m2) HRR peak=maximum of peak of HRR (kW/m2) THR=Total Heat Relase (MJ/m2) EHC=Effective Heat Release (MJ(kg)

(36) FIGRA and FPI were calculated manually. When the HRR vs time curve shows a second peak, and this second peak is higher in intensity than the first peak, it means a restart of burning. This occurrence is not desired, and it is therefore reported in the following tables as “Curve observation” arrow, as “NOT OK”.

(37) Materials used for preparing the tested compositions:

(38) Polymers

(39) Greenflex MQ 40 (Enichem, Ethylene vinyl acetate having a VA content=19%), hereafter “EVA” Exact 8201 (Dex Plastomers; ethylene 1-octene plastomer with hardenss Shore A=85 e MFR (190° C., 2,16 kg)=1 gr/10′), hereafter “Plastomer”
Metal Hydrates Magnifin H10 (Magnesium hydroxide by Albemarle), herafter “Mg(OH).sub.2” Alcan Superfine (Aluminum hydroxide by Alcan), hereafter “Al(OH).sub.3”
FR Additives Firebrake ZB (Zinc borate by Borax), hereafter “ZnB”
Metal Hypophosphite Phoslite IP-A (, Aluminium hypophosphite by Italmatch Chemicals), hereafter “IP-A”
Organic Phosphinate Exolit OP1230 (Aluminium diethylphosphinate, by Clariant), hereafter “OP1230”
Coupling Agent Compoline CO LL/05 (Auserpolimeri, LLDPE grafted with around 0.5-1% of maleic anhydride), hereafter “LLDPE-g-MAH”
Processing Aids Silmaprocess AL1142A (Silma Srl, silicon oil masterbatch 50% concentrated, based on LLDPE), hereafter “PDMS MB”

EXAMPLES

(40) In Examples 2 and 3 (indicated in the following Table 1 as E.2 and E.3) and Comparative Example 1,4,5,6,7,8,9 (indicated in the following Table 1 as C.1, C.4-C.9) (Table 1), cone calorimeter results are reported as well as the corresponding FIGRA and FPI for EVA based formulations at 65% total loading of filler by weight were calculated. Comparing C. 1 and C. 9, we can observe that FPI values of compositions containing Aluminum hypophosphite (C.9) are worse than those of the compositions containing an equal amount of Aluminum hydroxide (C.1). Comparing FIGRA and FPI values of C.7 and C.8 (realized according to WO 2009/010812) with corresponding values reported for C. 9, we can observe an improvement in flame retardancy properties, notwithstanding this improvement is not sufficient to be compared to C. 1 value. Increasing the ratio of Aluminum hydroxide to Aluminum hypophosphite (C.6, C.5, C.4) flame retardant properties decrease dramatically in terms of FIGRA and FPI values. Surprisingly, E. 2 and E. 3 show a great improvement over C. 1 in terms of FIGRA and FPI values.

(41) TABLE-US-00001 TABLE 1 C. 1 E. 2 E. 3 C. 4 C. 5 C. 6 C. 7 C. 8 C. 9 EVA 35% 35% 35%   35%   35%   35% 35% 35% 35% Al(OH)3 65% 63% 61% 52.5% 32.5% 12.5%  4%  2% IP-A  2%  4% 12.5% 32.5% 52.5% 61% 63% 65% TTI (sec) 96 86 77 48 54 51 55 50 52 HRR peak (kW/m2) 235 145 115 276 284 258 140 137 150 Time to HRR peak 169 145 108 123 130 128 137 133 137 (sec) FIGRA (lower, the 1.40 1.00 1.06 2.24 2.18 2.01 1.02 1.03 1.09 best) FPI (higher, the best) 0.41 0.59 0.67 0.44 0.46 0.50 0.39 0.36 0.35

(42) From the above data it is evident that, while FIGRA value of the compound according to C.9, comprising Aluminum hypophosphite as the sole Flame Retardant agent, is comparable with corresponding values of compounds according to E.2 and E.3 according to the present invention, FPI values of the compounds according to the invention, significantly improve.

(43) In Example 10 and Comparative Example 11 (Table 2) cone calorimeter results for plastomer based formulations at 55% loading of Magnesium hydroxide are reported. The calculated FIGRA and FIP values show the beneficial effect of the presence of Aluminum hypophosphite into the composition according to the present invention (according to Example 10).

(44) TABLE-US-00002 TABLE 2 Example 10 Comparative 11 Plastomer 39%  39% LLDPE-g-MAH 4%  4% PDMS MB 2%  2% IP-A 2% Mg(OH)2 53%  55% TTI (sec) 116 122 HRR medium (kW/m2) 73 78 HRR peak (kW/m2) 181 204 Time to HRR peak (sec) 175 170 THR (MJ/m2) 65 68 EHC (MJ/kg) 27 29 FIGRA (lower, the best) 1.03 1.20 FPI (higher, the best) 0.64 0.60 Curve observation OK OK

(45) In Table 3, Comparative Example 12 (C.12) to Comparative Example 21 (C.21), cone calorimeter results for EVA based formulation at 65% loadings of Magnesium hydroxide are reported.

(46) Calculated FIGRA and FPI values for polymer compositions according to Example 13, when compared to the results obtained through the polymer compositions according to Comparative Example 12 (C.12), show the beneficial effect of Aluminum hypophosphite into the polymer composition according to the invention.

(47) Similar performances are achievable with zinc borate instead of Aluminium hypophosphite, but only if zinco borate is loaded at 5% (C.14). When Zinc Borate is loaded at the corresponding concentration of Aluminium hypophosphite, i.e. 2%, a re start of flame is observed (C.15). Example 18 compared to Comparative Example 16 and Example 13 show that a coupling agent in presence of Aluminum hypophosphite, further improves FR performances. Comparative Example 17 compared to Example 18 shows that the presence of aluminum hypophosphite together with the metal hydroxide can give superior performances with respect to analogous compositions comprising organic metal phosphinate. Example 20 compared to Comparative Example 19 shows how the presence of a coupling agent and polydimethylsiloxane further improves FR performances in the presence of Aluminum hypophosphite together with the metal hydroxide, while its substitution with Zinc Borate in the same composition, does not afford similar performances (C. 21).

(48) TABLE-US-00003 TABLE 3 C. 12 E. 13 C. 14 C. 15 C. 16 C. 17 E. 18 C. 19 E. 20 C. 21 EVA 35% 35% 35% 35% 31% 31% 31% 29% 29%  29%  LLDPE-g-MAH  4%  4%  4%  4% 4% 4% PDMS MB  2% 2% 2% OP 1230  2% IP-A 2.00%    2% 2% Mg(OH)2 65% 63% 60% 63% 65% 63% 63% 65% 63%  60%  ZnB 5.0%   2% 5% TTI (sec) 96 102 96 111  134 138  113 130 116 126 HRR medium 91 67 65 77 88 90 72  71 56 73 (kW/m2) HRR peak 235 134 131 (108)  199 (184)  139 (150) 105 139 (kW/m2) Time to HRR 169 126 125 (122)  175 (203)  159 (218) 177 209 peak (sec) THR (MJ/m2) 56 65 64 50 53 61 63  48 53 47 EHC (MJ/kg) 24.6 27 28 22 22 25 26  21 23 22 FIGRA (lower, 1.39 1.06 1.05 — 1.14    0.91 0.87 — 0.59 0.66 the best) FPI (higher, the 0.40 0.76 0.73 — 0.67    0.75 0.81 — 1.1 0.91 best) Curve OK OK OK NOT OK NOT OK NOT OK OK observation OK OK OK

(49) In Table 4, cone calorimeter results for EVA based formulation at 65% loadings of Aluminum hydroxide are reported.

(50) Calculated FIGRA and FIP for Example 25 and Example 26 compared to corresponding results obtained according to Comparative Examples 22, 23 and 24 show the beneficial effect of Aluminum hypophosphite when used in combination with metal hydroxides.

(51) TABLE-US-00004 TABLE 4 C. 22 C. 23 C. 24 E. 25 E. 26 EVA 35% 35% 35% 35% 35% Al(OH)3 65% 60% 63% 63% 61% IP-A  2%  4% ZnB  5%  2% TTI (sec) 96 96 101 86 77 HRR medium 91 77 73 76 60 (kW/m2) HRR peak 235 177 (122) 145 115 (kW/m2) Time to HRR 169 142 (163) 145 108 peak (sec) THR (MJ/m2) 56 62 60 66 48 EHC (MJ/kg) 24.6 25 25 26 26 FIGRA (lower, 1.40 1.25 — 1.00 1.06 the best) FPI (higher, 0.41 0.54 — 0.59 0.67 the best) Curve OK OK NOT OK OK OK observation

(52) In Table 5, Comparative Examples 27, 28, 30 and Example 29, cone calorimeter results for EVA based formulation at 55% loadings of Aluminum hydroxide are reported.

(53) Calculated FIGRA and FIP values for polymeric compositions according to Comparative Examples 27 and 30 are compared to corresponding values obtained for polymeric compositions according to the present invention (Example 29). It is shown the beneficial effect of Aluminum hypophosphite when used in combination with metal hydroxides, according to the present invention.

(54) Comparative Example 28 is compared to Example 29. The comparison shows that aluminum hypophosphite used as flame retardant together with metal hydroxide gives superior performances to the polymeric compositions with respect to organic metal phosphinate used in corresponding formulations.

(55) TABLE-US-00005 TABLE 5 C. 27 C. 28 E. 29 C. 30 EVA 41% 41% 41% 41% LLDPE-g-MAH  4%  4%  4%  4% IP-A  2% A1(OH)3 55% 53% 53% 53% OP 1230  2% ZnB  2% TTI (sec) 92 114 95 101 HRR medium 102 116 91 91 (kW/m2) HRR peak 192 (238) 179 201 (kW/m2) Time to HRR 156 (175) 154 168 peak (sec) THR (MJ/m2) 64 66 62 62 EHC (MJ/kg) 25 28 24 24 FIGRA (lower, 1.23 1.36 1.16 1.20 the best) FPI (higher, 0.48 0.48 0.53 0.50 the best) Curve OK/NOT OK * NOT OK OK OK/NOT OK * observation * 3 curves out of 5 show a second peak higher than the first one

(56) In Table 6, Comparative Examples 31, 32, 34 and Example 33 according to the present invention, cone calorimeter results for EVA based formulation at 55% loadings of Magnesium hydroxide are reported.

(57) Calculated FIGRA and FIP values for compositions obtained according to Comparative Examples 31 and 32 are compared to corresponding values of polymeric compositions according to the present invention (Example 34). It is shown the beneficial effect of Aluminum hypophosphite used as FR agent in combination with metal hydroxide.

(58) Comparative Example 32 compared to Example 33 according to the invention shows that aluminum hypophosphite used as flame retardant agent in polymer formulations according to the present invention, is superior to organic metal phosphinate used in corresponding formulations.

(59) TABLE-US-00006 TABLE 6 C. 31 C. 32 E. 33 C. 34 EVA 41% 41% 41% 41% LLDPE-g-MAH  4%  4%  4%  4% IP-A  2% Mg(OH)2 55% 53% 53% 53% OP 1230  2% ZnB  2% TTI (sec) 127 121 110 129 HRR medium (kW/m2) 122 125 112 135 HRR peak (kW/m2) 314 (277) 256 (345) Time to HRR peak (sec) 231 (193) 192 (251) THR (MJ/m2) 65 66 64 64 EHC (MJ/kg) 27 27 25 26 FIGRA (lower, the best) 1.36 1.44 1.33 138 FPI (higher, the best) 0.40 0.44 0.43 0.37 Curve observation OK NOT OK OK NOT OK