GB2562167A - Fire retardant natural rubber based compositions - Google Patents
Fire retardant natural rubber based compositions Download PDFInfo
- Publication number
- GB2562167A GB2562167A GB1806256.2A GB201806256A GB2562167A GB 2562167 A GB2562167 A GB 2562167A GB 201806256 A GB201806256 A GB 201806256A GB 2562167 A GB2562167 A GB 2562167A
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- United Kingdom
- Prior art keywords
- flame retarding
- composition
- natural rubber
- rubber
- additive
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- 244000043261 Hevea brasiliensis Species 0.000 title claims abstract description 66
- 229920003052 natural elastomer Polymers 0.000 title claims abstract description 66
- 229920001194 natural rubber Polymers 0.000 title claims abstract description 66
- 239000000203 mixture Substances 0.000 title claims abstract description 47
- 239000003063 flame retardant Substances 0.000 title claims abstract description 33
- 150000001875 compounds Chemical class 0.000 claims abstract description 38
- 230000000979 retarding effect Effects 0.000 claims abstract description 36
- 229920001971 elastomer Polymers 0.000 claims abstract description 34
- 239000005060 rubber Substances 0.000 claims abstract description 33
- 239000000654 additive Substances 0.000 claims abstract description 31
- 230000000996 additive effect Effects 0.000 claims abstract description 26
- 239000011256 inorganic filler Substances 0.000 claims abstract description 22
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 6
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims abstract description 5
- 239000000347 magnesium hydroxide Substances 0.000 claims abstract description 5
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims abstract description 5
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 claims abstract description 5
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims abstract description 4
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims abstract description 4
- 229910021502 aluminium hydroxide Inorganic materials 0.000 claims abstract description 4
- DXZMANYCMVCPIM-UHFFFAOYSA-L zinc;diethylphosphinate Chemical compound [Zn+2].CCP([O-])(=O)CC.CCP([O-])(=O)CC DXZMANYCMVCPIM-UHFFFAOYSA-L 0.000 claims abstract description 4
- 229940071182 stannate Drugs 0.000 claims abstract description 3
- 239000011701 zinc Substances 0.000 claims abstract description 3
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 3
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical compound [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 abstract description 6
- ZSFDBVJMDCMTBM-UHFFFAOYSA-N ethane-1,2-diamine;phosphoric acid Chemical compound NCCN.OP(O)(O)=O ZSFDBVJMDCMTBM-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000463 material Substances 0.000 description 16
- 238000000034 method Methods 0.000 description 11
- 238000006735 epoxidation reaction Methods 0.000 description 10
- 238000000576 coating method Methods 0.000 description 7
- 230000004580 weight loss Effects 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000000779 smoke Substances 0.000 description 5
- 229920002943 EPDM rubber Polymers 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920003051 synthetic elastomer Polymers 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000004114 Ammonium polyphosphate Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 2
- 229920001276 ammonium polyphosphate Polymers 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000009408 flooring Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 150000004965 peroxy acids Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- -1 alkyl hydroperoxide Chemical compound 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 238000007416 differential thermogravimetric analysis Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920006168 hydrated nitrile rubber Polymers 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000004967 organic peroxy acids Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 1
- 230000009044 synergistic interaction Effects 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 229940117958 vinyl acetate Drugs 0.000 description 1
- BHTBHKFULNTCHQ-UHFFFAOYSA-H zinc;tin(4+);hexahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Zn+2].[Sn+4] BHTBHKFULNTCHQ-UHFFFAOYSA-H 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0066—Flame-proofing or flame-retarding additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
- C08K3/013—Fillers, pigments or reinforcing additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/10—Metal compounds
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/5399—Phosphorus bound to nitrogen
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L15/00—Compositions of rubber derivatives
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- C08L7/00—Compositions of natural rubber
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2217—Oxides; Hydroxides of metals of magnesium
- C08K2003/2224—Magnesium hydroxide
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
- C08K2003/387—Borates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/02—Flame or fire retardant/resistant
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/22—Halogen free composition
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/28—Non-macromolecular organic substances
- C08L2666/36—Nitrogen-containing compounds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/28—Non-macromolecular organic substances
- C08L2666/40—Phosphorus-containing compounds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/54—Inorganic substances
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- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/66—Substances characterised by their function in the composition
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- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/66—Substances characterised by their function in the composition
- C08L2666/72—Fillers; Inorganic pigments; Reinforcing additives
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- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/66—Substances characterised by their function in the composition
- C08L2666/84—Flame-proofing or flame-retarding additives
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
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- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A flame retardant rubber composition comprises a rubber compound containing epoxidised natural rubber (ENR), inorganic filler, and a flame retarding additive. Typically, the inorganic filler is present in an amount of 40-65 wt.% and may be aluminium hydroxide, magnesium hydroxide, zinc borate, zinc hydroxyl stannate, or silica. The flame retarding additive may be an intumescent additive and may be an organic phosphorus-nitrogen-containing compound, such as ethylene diamine phosphate. The rubber compound may contain 25 mol.% or 50 mol.% epoxidised natural rubber. A flame retarding composition comprising epoxidised natural rubber, inorganic filler, and an additive is also disclosed. A further halogen-free flame retarding composition comprising epoxidised natural rubber, inorganic filler, and an organic phosphorus-nitrogen-containing additive is claimed.
Description
(71) Applicant(s):
Lembaga Getah Malaysia
15th Floor 148 Jalan Ampang, Kuala Lumpur 50450, Malaysia
Tun Abdul Razak Research Centre (Incorporated in the United Kingdom) BRICKENDONBURY, Hertfordshire, SG13 8NL, United Kingdom (51) INT CL:
C08K5/00 (2006.01) C08K3/10 (2018.01) C08K 5/521 (2006.01) C08L 7/00 (2006.01) (56) Documents Cited:
EP 1361249 A2 CN 106317519 A CN 105860506 A (58) Field of Search:
INT CL C08K, C08L Other: WPI, EPODOC
C08K 3/013 (2018.01) C08K 5/17 (2006.01) C08K 13/02 (2006.01) C08L 15/00 (2006.01)
CN 106479007 A CN 105860510 A CN 105754171 A (72) Inventor(s):
Marina Fernando (74) Agent and/or Address for Service:
Williams Powell
Staple Inn, LONDON, WC1V 7QH, United Kingdom (54) Title of the Invention: Fire retardant natural rubber based compositions Abstract Title: Fire retardant rubber composition (57) Aflame retardant rubber composition comprises a rubber compound containing epoxidised natural rubber (ENR), inorganic filler, and a flame retarding additive. Typically, the inorganic filler is present in an amount of 40-65 wt.% and may be aluminium hydroxide, magnesium hydroxide, zinc borate, zinc hydroxyl stannate, or silica. The flame retarding additive may be an intumescent additive and may be an organic phosphorus-nitrogen-containing compound, such as ethylene diamine phosphate. The rubber compound may contain 25 mol.% or 50 mol.% epoxidised natural rubber. Aflame retarding composition comprising epoxidised natural rubber, inorganic filler, and an additive is also disclosed. A further halogen-free flame retarding composition comprising epoxidised natural rubber, inorganic filler, and an organic phosphorus-nitrogen-containing additive is claimed.
1/4
IR | NR(SMR 10) | DPNR | ENR50 | |
max. % weight loss rate, (%wt. loss/sec) | 0.82 | 0.88 | 0.82 | 0.72 |
Temperature at maximum wt. loss, (°C) | 389 | 383 | 389 | 412 |
FIGURE 1
2/4
Standard | Requirement | Measurement on | |
ENR 50 based, Natural-FR compound | |||
Smoke density, | EN5659-2;25kW/m2 | <150 | 97 (9mm) |
Ds max | |||
Smoke toxicity, CITg | EN5659-2;25kW/m2 | <0.75 | 0.22 (9mm) |
Flame Spread,CHF | EN ISO 9239-1, kW/m2 | >8 | >10.8 (9mm) |
Flammability | BS EN ISO 4589- 2:1999 | >32 | 54.3 (6mm) 48.3(4mm) |
FIGURE 2
3/4
SMR 10 | ENR50 | ||
max. % weight loss rate, (%wt. loss/sec) | 0.19 | 0.16 | |
Temperature at maximum wt.loss, (°C) | 382 | 412 |
FIGURE 3
4/4
ENR50 | EPDM/EVA | ||
max. % weight loss rate, (%wt. loss/sec) | 0.06 | 0.07 | |
Temperature at maximum wt.loss, (°C) | 419 | 370 |
FIGURE 4
FIRE RETARDANT NATURAL RUBBER BASED COMPOSITIONS
Field of Invention
The present invention relates to fire retardant natural rubber compositions, and more particularly to halogen-free fire retardant compositions based on epoxidized natural rubber (ENR).
Background of the Invention
In the industrial rubber products sector, new requirements for reaction to fire tests on materials are in place, such as in the construction and transportation industries. Fire statistics clearly indicate that more lives are lost by smoke density, which impedes escape and is toxic by inhalation. Legislation on the use of materials exists in several industrial sectors worldwide to improve the safety of the public and safeguard structures. One such example is the requirements in the rail sector where stringent testing is needed as part of a product acceptance phase. For example, in the rail sector in Europe the new harmonized EU standard Railway applications-Fire protection on railway vehicles, Part 2: Requirements for fire behaviour of materials and components - EN45545-2 (2013) lists requirements for flame resistance of materials used in rolling stock. In this standard hazard level categories are indicated, based on a matrix which consider the train design and the operating environment. The defined material tests, consider many aspects of fire development and growth such as, the heat released from a burning material, the extent of flame spread once initiated, the ease of ignition as well as the smoke density and toxicity. Current use halogen free, low smoke, low toxic emission rubbers are based on synthetic elastomers, and do not contribute to a low carbon economy, thus the present invention provides a greener route to achieving material flammability resistance.
EP 2196492B1 discloses a method of protecting an elastomeric body with fire retardant coating. The fire retardant coating has been successfully commercialized and is in use to protect rubber springs in the rail bogie. The fire retardant coating is halogen-free and comprises a fire retardant substance and a binder material. The fire retardant coating can be adapted to include at least one material from the group zinc borate, aluminium trihydrate, expandable graphite, ammonium polyphosphate, magnesium hydroxide, montmorillonite clay and red phosphorous. Similarly, it is claimed that the binder material can be selected from the group consisting of NR, EPDM ENR, SBR, PU, NBR and HNBR.
WO 2014019008 discloses a polymeric composition suitable for use as a coating containing a vinyl-acetate containing thermoplastic polymer and an unsaturated elastomer vulcanized with sulphur and a method of application of the coating thereof is claimed.
The above coatings approach is not based on natural resource derived polymers and accordingly there is a commercial need for the provision of halogen-free natural rubber based fire retardant compositions. These will have potential applications as an outer layer in rubber to metal-bonded products as well as to be used directly on its own and not as an outer layer, in other suitable applications such as flooring.
Summary of the Invention
An aspect of the present invention provides a halogen-free flame retarding composition comprising an epoxidized natural rubber, inorganic fillers in range of 40 to 65 in weight percentage; and an organic nitrogen-phosphorous containing additive .
Another aspect of the present invention provides a flame retarding rubber composition having hardness of 90 IRHD, 50 mol % epoxidized natural rubber and suitable for entrance matting in public or private establishments.
A further aspect of the present invention provides a flame retarding rubber composition having hardness of 85 IRHD, 50 mol % epoxidized natural rubber and suitable for coloured floor tiles in public areas.
A further aspect of the present invention provides a flame retarding rubber composition having hardness of 78 IRHD, 25 mol % epoxidized natural rubber and suitable for use as an outer fire retardant layer in anti-vibration components.
Brief Description of the Drawings
Embodiments of the present invention are described below, by way of example only, with reference to the accompanying drawings, in which:
Figure 1 shows a table illustrating TGA/DTG data for raw rubbers in air at 30°C/min, according to an embodiment herein;
Figure 2 shows a table illustrating fire test data on ENR 50 based fire retardant entrance matting compound (Natural-FR) , according to an embodiment herein;
Figure 3 shows a table illustrating TGA/DTG data on typical fire retardant compounds used in entrance matting and a SMR 10 compound based on the same formulation as the ENR 50 compound measured in air at a rate of 30°C/min, according to an embodiment herein; and
Figure 4 shows a table illustrating TGA/DTG data on current fire retardant compounds used in entrance matting and the ENR 50 compound measured in air at a rate of 10°C/min
Detailed Description of the Preferred Embodiments
The teachings herein relate generally to flame-retardant rubber compositions to produce rubber articles in industrial applications, which needs to meet current requirements for fire safe materials. The flame-retardant rubber compositions as described can be used in making articles that can be used at public places wherein flame resistance is required to prevent fire initiation and spread.
The preferred embodiments provide a halogen-free fire retardant composition that comprises epoxidised natural rubber with varying degrees of epoxidation, inorganic fillers in the range 40% - 65% by weight, and an organic nitrogenphosphorous containing additive with possible synergism with epoxidised natural rubber.
The preferred flame/fire retardant rubber composition described herein is made using natural rubber based compound and more specifically an epoxidized natural rubber. The natural rubber based compound advantageously consists of an epoxidized natural rubber (ENR). Since no synthetic rubber derived from petroleum resources is used, it is possible to reduce the amount of use of materials derived from petroleum resources .
Thermal decomposition data on the raw ENR 50 rubber using thermogravimetric analysis and differential thermogravimetric analysis (TGA/DTG) when compared with other natural rubbers demonstrates its superior performance as shown in Figure 1. The maximum rate of weight loss for ENR is 12% lower than synthetic polyisoprene (IR) and deproteinised natural rubber (DPNR) and 18% lower than field grade natural rubber (NR), SMR 10. Similarly, the temperature at which the maximum decomposition occurs is also higher for ENR 50 by 23°C and 29°C compared with IR and NR (SMR 10).
The epoxidized natural rubber (ENR) is a modified natural rubber, in which unsaturated double bonds of a natural rubber (NR) are epoxidized. Epoxidation increases the glass transition temperature by approximately 1° for each mole percent epoxidation, the resulting polymer as compared with NR has improved damping, better oil resistance, reduced gas permeability, improved interaction with polar fillers such as silica resulting in improved wet grip. The ability to strain crystallize is however retained up to 75% epoxidation and epoxidation reduces the storage hardening. Unlike NR, premastication of ENR is not generally required as the breakdown on a mill or in an internal mixer is rapid. ENR is normally compounded with either semi-EV and EV cure. A base is added to ENR recipes to improve the ageing behaviour of ENR based compounds.
With respect to the epoxidized natural rubber (ENR), those commercially available may be used such as Ekoprena™ as manufactured by FGV in Malaysia, or those formed by epoxidizing a natural rubber (NR) may be used. With respect to the method for epoxidizing the natural rubber (NR), not particularly limited, for example, a chlorohydrin method, a direct oxidizing method, a hydrogen peroxide method, an alkyl hydroperoxide method and a peroxide method may be used. With respect to the peroxide method, for example, a method may be used in which, for example, an emulsion of a natural rubber is allowed to react with an organic peroxy acid, such as acetic peroxy acid and formic peroxy acid, serving as an epoxidizing agent.
The epoxidation ratio of the epoxidized natural rubber (ENR) is preferably set to 5 mol % or more, preferably, to 10 mol % or more. In the present specification, the epoxidation ratio refers to a ratio of the number of epoxidized double bonds among all the number of double bonds in a natural rubber prior to the epoxidization, and this ratio is found by using, for example, a titration analysis and a nuclear magnetic resonance (NMR) analysis. With respect to the epoxidized natural rubber (ENR), typically, an epoxidized natural rubber having an epoxidation ratio of 25 mol %, or an epoxidized natural rubber having an epoxidation ratio of 50 mol %, may be used in fire retardant formulations
Fire retardant rubber compound based on epoxidised natural rubber thus provides a fully compliant rubber compound that can meet current reaction to fire tests specifications on materials for a number of rubber products. Data showing the compliance of an entrance matting compound based on epoxidized natural rubber is shown in Figure 2.
The rubber composition according to the preferred embodiment of the present invention comprises one or more inorganic fillers. The inorganic filler is preferably blended in a range from 40 to 65 parts by weight relative to the total weight of the compound. The compounding amount of the inorganic filler is preferably set to 40 parts by weight or more, preferably to 50 parts by mass or more, and is also preferably set to 65 parts by mass or less.
The inorganic filler consists of at least one material selected from the group consisting of, aluminium hydroxide, magnesium hydroxide, zinc borate, zinc hydroxy stannate and silica .
In the preferred embodiments, in addition to inorganic fillers, organic phosphorus-nitrogen compound, ethylene diamine phosphate (commercially available from Polymer Tailoring, UK) are used as an additive in the epoxidized natural rubber to confer the required flame retardancy to composition. These types of fire retardants can be active either in the condensed or the vapour-phase or both. Phosphorus has very good flame retarding properties and it is believed that the evolution of ammonia from the decomposition of the nitrogen-phosphorus additive, a non-flammable gas, dilutes the fire gases. The decomposition of the nitrogenphosphorus additive results also in phosphoric acid which encourages char formation.
In the preferred embodiments, the range of fillers and fire retardant additives specified, when used in combination were found to act with epoxidised natural rubber in a manner to give enhanced fire retardant activity. The addition of fire retardant additives delays the thermal decomposition of the epoxidised natural rubber based compound when compared with a similar compound based on fire retardant natural rubber as shown in Figure 3. This is illustrated by data showing that the maximum rate of weight loss is significantly reduced by the addition of FR additives (comparing values in Figure 1 and Figure 3) but that the ENR 50 based compound has a lower maximum rate of weight loss as compared with the NR based compound. The maximum temperature at which the maximum weight loss rate occurs, is higher for the ENR 50 compound than the NR based compound indicating the delayed thermal decomposition of the ENR 50 compound.
The preferred embodiments comprising epoxidised natural rubber with varying degrees of epoxidation, inorganic fillers in the range 40% - 65% by weight, and an organic phosphorousnitrogen containing additive are believed to deliver enhanced fire retardant properties through synergistic interactions between the various fillers, fire retardant additives and the epoxidised natural rubber.
According to an embodiment of the present invention a flame retarding rubber composition having hardness of 90 IRHD comprising an epoxidized natural rubber, an inorganic filler in range of 40 to 65 in weight percentage and an organic phosphorous-nitrogen containing additive is suitable for suitable for entrance matting in metro stations and other areas where fire retardant material requirements are present. Figure 4 shows thermal decomposition data (TGA/DTG) on a fire retardant compound in current use in entrance matting manufacture made from an ENR 50 based compound and a comparison with a fire compliant EPDM/EVA compound also used currently in entrance matting manufacture. The ENR 50 based compound shows improved decomposition characteristics as compared with the EPDM/EVA compound. Furthermore, the ENR 50 compound meets all requirements in reaction to fire tests
in place specified | for materials used as in BS EN 45545-2:2013. | flooring | for | railways | as |
According | to an embodiment of the present | invention flame | |||
retarding | rubber composition has | hardness | of | 85 IRHD | and |
includes an epoxidized natural rubber, an inorganic filler in range of 40 to 65 in weight percentage or by mass, and an organic phosphorous-nitrogen containing additives, such as ethylene diamine phosphate, ammonium polyphosphate, melamine phosphate, melamine polyphosphate or their mixtures, are suitable for coloured floor tiles in public areas.
According to an embodiment of the present invention flame retarding rubber composition having hardness of 78 IRHD comprising an epoxidized natural rubber, an inorganic filler in range of 40 to 65 in weight percentage and an organic phosphorous-nitrogen containing one additive is suitable for use as an outer fire retardant layer in anti-vibration components .
A Typical FR formulation based on ENR 50 formulation consists of the following:
Ingredient | % w/w |
ENR 50 (Ekoprena™ 50) | 20 - 30 |
Carbon Black (or silica) | 0-10 (or 0 - 20) |
Inorganic FR fillers | 40 - 65 | |
Organic phosphorous-nitrogen | 0-10 | |
additive | ||
Antidegradants, | activators, | 0.5 - 5.0 |
base, colorant | ||
Cure System | ||
Sulphur | 0.25 - 0.5 | |
Sulfenamide | 0.25-0.5 | |
PVI | 0 - 0.1 |
While various embodiments are disclosed herein, it should be understood that they have been presented by way of example only, and not limitation. It will be apparent to persons skilled in the relevant art that various changes in form and detail may be made therein without departing from the spirit and scope of the methods and systems disclosed herein. Thus, the breadth and scope of the claims should not be limited by any of the example embodiments disclosed herein.
Claims (14)
1. A flame retarding rubber composition comprising:
a rubber compound containing an epoxidized natural rubber;
inorganic fillers in range of 40 to 65 parts by mass; and a flame retarding additive.
2. The flame retarding composition of claim 1, wherein said additive is a phosphorous-nitrogen containing additive.
3. The flame retarding composition of claim 1, wherein the flame retarding additive is an organic phosphorousnitrogen containing compound.
4. The flame retarding composition of claim 1, 2 or 3, where in the flame retarding rubber composition has a hardness of 90 IRHD.
5. The flame retarding composition of claim 4, wherein the rubber compound has 50 mol % epoxidized natural rubber.
6. The flame retarding composition of claim 1, 2, or 3, where in the flame retarding rubber composition has hardness of 85 IRHD.
7. The flame retarding composition of claim 6, wherein the rubber compound has 50 mol % epoxidized natural rubber.
8. The flame retarding composition of claim 1, 2 or 3, where in the flame retarding rubber composition has hardness of 78 IRHD.
9. The flame retarding composition of claim 8, wherein the rubber compound has 25 mol % epoxidized natural rubber.
10. The flame retarding composition of any preceding claim, wherein the flame retarding additive is an intumescent flame retardant additive.
11. The flame retarding composition of any preceding claim, wherein the inorganic filler is selected from at least aluminium hydroxide, magnesium hydroxide, zinc borate, zinc hydroxyl stannate and silica.
12. A flame retarding composition comprising:
a natural rubber compound consisting of an epoxidized natural rubber;
an inorganic filler in range of 40 to 65 parts by mass; and an additive.
13. A halogen free flame retarding composition comprising:
an epoxidized natural rubber;
an inorganic filler in range of 40 to 65 parts by mass; and an organic phosphorous-nitrogen containing additive .
14. The flame retarding composition of claim 13, where in the flame retarding rubber composition having hardness of 90 IRHD.
Intellectual
Property
Office
Application No: GB 1806256.2 Examiner: Dr Paul Minton
Applications Claiming Priority (1)
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MYPI2017000644A MY182405A (en) | 2017-05-02 | 2017-05-02 | Fire retardant natural rubber based compositions |
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GB2562167A true GB2562167A (en) | 2018-11-07 |
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CN112500616B (en) * | 2020-11-20 | 2023-03-24 | 株洲时代新材料科技股份有限公司 | Flame-retardant rubber for track vibration damper and preparation method thereof |
CN116731408A (en) * | 2023-07-31 | 2023-09-12 | 云南国为机械科技有限公司 | Rubber shock pad and preparation process thereof |
Citations (6)
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EP1361249A2 (en) * | 2002-05-07 | 2003-11-12 | Armstrong World Industries, Inc. | Thermoplastic elastomer |
CN105754171A (en) * | 2016-03-16 | 2016-07-13 | 吉林师范大学 | High-strength wear-resistant flame-retardant modified natural rubber composite |
CN105860506A (en) * | 2016-04-19 | 2016-08-17 | 滁州环球聚氨酯科技有限公司 | Composite flame retardant modified polyurethane composite material |
CN105860510A (en) * | 2016-04-19 | 2016-08-17 | 滁州环球聚氨酯科技有限公司 | High-flame-retardancy polyurethane composite material |
CN106317519A (en) * | 2016-08-11 | 2017-01-11 | 芜湖诚通自动化设备有限公司 | Anti-aging and flame-retardant power cable sheath material |
CN106479007A (en) * | 2016-10-25 | 2017-03-08 | 姹や寒 | A kind of wearable environment protection type power cable sheath material |
-
2017
- 2017-05-02 MY MYPI2017000644A patent/MY182405A/en unknown
-
2018
- 2018-04-17 GB GB1806256.2A patent/GB2562167A/en not_active Withdrawn
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1361249A2 (en) * | 2002-05-07 | 2003-11-12 | Armstrong World Industries, Inc. | Thermoplastic elastomer |
CN105754171A (en) * | 2016-03-16 | 2016-07-13 | 吉林师范大学 | High-strength wear-resistant flame-retardant modified natural rubber composite |
CN105860506A (en) * | 2016-04-19 | 2016-08-17 | 滁州环球聚氨酯科技有限公司 | Composite flame retardant modified polyurethane composite material |
CN105860510A (en) * | 2016-04-19 | 2016-08-17 | 滁州环球聚氨酯科技有限公司 | High-flame-retardancy polyurethane composite material |
CN106317519A (en) * | 2016-08-11 | 2017-01-11 | 芜湖诚通自动化设备有限公司 | Anti-aging and flame-retardant power cable sheath material |
CN106479007A (en) * | 2016-10-25 | 2017-03-08 | 姹や寒 | A kind of wearable environment protection type power cable sheath material |
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MY182405A (en) | 2021-01-25 |
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