CA2025122A1 - Smoke suppressed flame retardant unsaturated polyester resin compositions - Google Patents
Smoke suppressed flame retardant unsaturated polyester resin compositionsInfo
- Publication number
- CA2025122A1 CA2025122A1 CA002025122A CA2025122A CA2025122A1 CA 2025122 A1 CA2025122 A1 CA 2025122A1 CA 002025122 A CA002025122 A CA 002025122A CA 2025122 A CA2025122 A CA 2025122A CA 2025122 A1 CA2025122 A1 CA 2025122A1
- Authority
- CA
- Canada
- Prior art keywords
- flame retardant
- composition
- chain
- retardant agent
- phosphate compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 68
- 239000003063 flame retardant Substances 0.000 title claims abstract description 25
- 239000000779 smoke Substances 0.000 title claims abstract description 25
- 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 title claims abstract description 22
- 229920006337 unsaturated polyester resin Polymers 0.000 title description 4
- -1 bicyclic phosphate compound Chemical class 0.000 claims abstract description 32
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 30
- 239000004634 thermosetting polymer Substances 0.000 claims abstract description 18
- 239000010452 phosphate Substances 0.000 claims abstract description 17
- 229920006305 unsaturated polyester Polymers 0.000 claims abstract description 12
- 235000021317 phosphate Nutrition 0.000 claims description 29
- 150000001875 compounds Chemical class 0.000 claims description 26
- 239000012757 flame retardant agent Substances 0.000 claims description 22
- 239000011347 resin Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Chemical class 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 5
- 150000004677 hydrates Chemical class 0.000 claims description 5
- 239000000347 magnesium hydroxide Substances 0.000 claims description 5
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 5
- 229920000647 polyepoxide Polymers 0.000 claims description 5
- 150000004684 trihydrates Chemical class 0.000 claims description 5
- 229920001567 vinyl ester resin Polymers 0.000 claims description 5
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 239000003365 glass fiber Substances 0.000 claims description 4
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical class [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 4
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 4
- 230000002787 reinforcement Effects 0.000 claims description 4
- 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 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- PKTNMTDLDLSRDE-UHFFFAOYSA-N C1OC2(P(=O)=O)OCC1(CO)CO2 Chemical compound C1OC2(P(=O)=O)OCC1(CO)CO2 PKTNMTDLDLSRDE-UHFFFAOYSA-N 0.000 claims description 3
- 150000001642 boronic acid derivatives Chemical class 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000011342 resin composition Substances 0.000 claims description 3
- 229920001187 thermosetting polymer Polymers 0.000 abstract description 11
- 239000000463 material Substances 0.000 abstract description 2
- 239000000654 additive Substances 0.000 description 17
- 229920001276 ammonium polyphosphate Polymers 0.000 description 11
- 230000000996 additive effect Effects 0.000 description 9
- 125000002619 bicyclic group Chemical group 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 229910052787 antimony Inorganic materials 0.000 description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- UNYOJUYSNFGNDV-UHFFFAOYSA-M magnesium monohydroxide Chemical compound [Mg]O UNYOJUYSNFGNDV-UHFFFAOYSA-M 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 230000001629 suppression Effects 0.000 description 3
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- FWKIOSWFVPOWSM-UHFFFAOYSA-N 1,1,12,12,12-pentabromododecylbenzene Chemical compound BrC(Br)(Br)CCCCCCCCCCC(Br)(Br)C1=CC=CC=C1 FWKIOSWFVPOWSM-UHFFFAOYSA-N 0.000 description 1
- UZOSVZSBPTTWIG-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-chlorocyclohexane Chemical compound ClC1C(Br)C(Br)C(Br)C(Br)C1Br UZOSVZSBPTTWIG-UHFFFAOYSA-N 0.000 description 1
- FIAXCDIQXHJNIX-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-ethylbenzene Chemical compound CCC1=C(Br)C(Br)=C(Br)C(Br)=C1Br FIAXCDIQXHJNIX-UHFFFAOYSA-N 0.000 description 1
- ACRQLFSHISNWRY-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-phenoxybenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=CC=CC=C1 ACRQLFSHISNWRY-UHFFFAOYSA-N 0.000 description 1
- ORYGKUIDIMIRNN-UHFFFAOYSA-N 1,2,3,4-tetrabromo-5-(2,3,4,5-tetrabromophenoxy)benzene Chemical compound BrC1=C(Br)C(Br)=CC(OC=2C(=C(Br)C(Br)=C(Br)C=2)Br)=C1Br ORYGKUIDIMIRNN-UHFFFAOYSA-N 0.000 description 1
- NQKVVCRUKCIGHX-UHFFFAOYSA-N 1,2,3-tribromo-4-[1-[2-(9,9-dibromononyl)phenoxy]ethoxy]benzene Chemical compound C=1C=C(Br)C(Br)=C(Br)C=1OC(C)OC1=CC=CC=C1CCCCCCCCC(Br)Br NQKVVCRUKCIGHX-UHFFFAOYSA-N 0.000 description 1
- DEIGXXQKDWULML-UHFFFAOYSA-N 1,2,5,6,9,10-hexabromocyclododecane Chemical compound BrC1CCC(Br)C(Br)CCC(Br)C(Br)CCC1Br DEIGXXQKDWULML-UHFFFAOYSA-N 0.000 description 1
- YATIGPZCMOYEGE-UHFFFAOYSA-N 1,3,5-tribromo-2-[2-(2,4,6-tribromophenoxy)ethoxy]benzene Chemical compound BrC1=CC(Br)=CC(Br)=C1OCCOC1=C(Br)C=C(Br)C=C1Br YATIGPZCMOYEGE-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- RYUJRXVZSJCHDZ-UHFFFAOYSA-N 8-methylnonyl diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)(OCCCCCCCC(C)C)OC1=CC=CC=C1 RYUJRXVZSJCHDZ-UHFFFAOYSA-N 0.000 description 1
- 239000004114 Ammonium polyphosphate Substances 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- YBAIRXAJHLSFLB-UHFFFAOYSA-N BrC1(CCC(CC1)CC(Br)Br)Br Chemical compound BrC1(CCC(CC1)CC(Br)Br)Br YBAIRXAJHLSFLB-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 238000005698 Diels-Alder reaction Methods 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical group 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- UUEDINPOVKWVAZ-UHFFFAOYSA-N bis(2-ethylhexyl) 3,4,5,6-tetrabromobenzene-1,2-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1=C(Br)C(Br)=C(Br)C(Br)=C1C(=O)OCC(CC)CCCC UUEDINPOVKWVAZ-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical class C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 1
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 1
- QRBLPTJJQNRVAJ-UHFFFAOYSA-N dioctyl 3,4,5,6-tetrabromobenzene-1,2-dicarboxylate Chemical compound CCCCCCCCOC(=O)C1=C(Br)C(Br)=C(Br)C(Br)=C1C(=O)OCCCCCCCC QRBLPTJJQNRVAJ-UHFFFAOYSA-N 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 238000007706 flame test Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000009787 hand lay-up Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 229920006216 polyvinyl aromatic Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- 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
- C08K5/527—Cyclic esters
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
GL354.APP
ABSTRACT
Smoke suppressed flame retardant thermoset resin compositions comprise bicyclic phosphate compound(s), flame retardant(s) and unsaturated polyester or other thermoset materials. These compositions exhibit a reduced tendency to smoke under conditions of burning.
ABSTRACT
Smoke suppressed flame retardant thermoset resin compositions comprise bicyclic phosphate compound(s), flame retardant(s) and unsaturated polyester or other thermoset materials. These compositions exhibit a reduced tendency to smoke under conditions of burning.
Description
C.L354.APP
A ~; ~
CROSS-REFERRNCE
This application is a continuat:ion-in-part of co-pending application Serial No. 289,973, filed December 22, 1988.
BACKGROUND OF THE I NVENT I ON
Field of the Invention. This invention relates to thermoset polymers and specifically to additiv,es which provide smoke suppression to unsaturatad polyester ("UPE") and other thermoset resin compositions and anhance the effect of flame retardant agents incorporated therewith.
Description of the Prior Art. It is known in the art that the flammability of thermoset resins such as unsaturated polyesters can be reduced by incorporation of a flame retardant agent. Typical flame retardant agents include reactive ur additive halogenated organic compounds, inorganic fillers, and special formulations based on phosphorous and ammonium salts.
Although efficient in suppressing the rate of combustion in a resin system, most flame retardants tend to affect adversely one or more key properties of the resin. For example, many flame retardant additives are ineffective at producing low smoke ("smoXe suppressed") formulations.
Recent public awareness about risk and hazard assessment during fire situations, and technical limitations of conventional flame retardant additives warrant a need for improved 1ame retardant thermoset compositions. In particular, a need exists for a thermoset composition that passes flammability standards with low smoke and combustion by-product formation, and does not detract from overall polymer performance.
.
GL354.APP
A ~; ~
CROSS-REFERRNCE
This application is a continuat:ion-in-part of co-pending application Serial No. 289,973, filed December 22, 1988.
BACKGROUND OF THE I NVENT I ON
Field of the Invention. This invention relates to thermoset polymers and specifically to additiv,es which provide smoke suppression to unsaturatad polyester ("UPE") and other thermoset resin compositions and anhance the effect of flame retardant agents incorporated therewith.
Description of the Prior Art. It is known in the art that the flammability of thermoset resins such as unsaturated polyesters can be reduced by incorporation of a flame retardant agent. Typical flame retardant agents include reactive ur additive halogenated organic compounds, inorganic fillers, and special formulations based on phosphorous and ammonium salts.
Although efficient in suppressing the rate of combustion in a resin system, most flame retardants tend to affect adversely one or more key properties of the resin. For example, many flame retardant additives are ineffective at producing low smoke ("smoXe suppressed") formulations.
Recent public awareness about risk and hazard assessment during fire situations, and technical limitations of conventional flame retardant additives warrant a need for improved 1ame retardant thermoset compositions. In particular, a need exists for a thermoset composition that passes flammability standards with low smoke and combustion by-product formation, and does not detract from overall polymer performance.
.
GL354.APP
2 ~ j r;~ r J
Many prior art references describe the use of a variety of smoke additives in unsaturated polyesters. Modern Plastics Encyclopedia, Vol. 63, No. lOA, McGraw-Hill, Inc., pp. 179-180 (1986). However, the selection of a suitable smoXe suppressant for thermoset resins is not predictable. Selection is particu-larly difficult when flame retardants are employed, exacerbated by the complex interaction between the polymer and the flame retardant agent.
Hechenbleikner, et al. describe in U.S. Patent No. 3,293,327 the production of bicyclic phosphites, phosphonates, thiophosphates, and selenophosphates. These compositions are said to be stabilizers for vinyl halide resins. They are alleged to be useful as heat stabilizers for vinyl chloride resin, and as antioxidants for fats and oils. The Hechenbleikner patent does not specify the use of bicyclic phosphates to achieve low smoke thermoset resin compositions, nor does it disclose that cyclic phosphates of the present invention coul~ be used with flame retardant agents to produce smoke suppressed flame retardant thermoset compositions.
British Patent No. g99,793 ~escribes a process for producing organic phosphates by ~ubjecting organic phosphites to reaction with peracetic acid. This patent shows a method for producing the most preferred bicyclic phosphate of the present invention, 2,6,7-trioxa-l-phosphobicyclo~2.2.2]-octane-4-methanol-l-oxide and teaches the use of acetal ring-containing phosphates as plasticizers or functional fluids. The British patent, however, does not disclose the present invention. It does not mention ' ', :~,,, , ~
GL354.APP
2~ 3.~. 2 ~
~ yclic phosphates as being useful for flame retardant thermoset resins, nor that the most preferred bicyclic phosphate of the present invention can be used with flame retardant-additives to yield improved thermoset compositions.
Hills, et al. describe in U.S. Patent No. 3,873,496 a 1ame retardant polyester composition which contains 5 to 25 percent of a hydroxymethyl bicyclic phosphate compound as a ~lame retardant additive. Hills did not observe the ability for bicyclic phos-phates to act as smoke suppressors for thermoset resin compositions which employ other compounds as the primary flame retardant additive.
Halpern, e~ al. describe in U.S. Patent No. 4,341,694 a composition comprising 2,6,7-trioxa-1-phosphobicyclo[2.~.2]-octane-4-methanol-1-oxide and a nitrogen-containing co-additive, which are intumescent and are adaptable to flame retard polyolefins, polyvinylaromatic resins, polycarbonates, PVC and blends thereof. Halpern did not observe any smoke suppression of the present invention.
Parr, et al. describe in U.S. Patent No. 4,801,625 a flame resistant composition having (1) an organic polymeric substance in intimate contact with (2) a bicyclic phosphorous compound, and (3) a gas producing compound. Parr is silent on the use of bicyclic compounds to attain smoke suppressed flame retardant thermoset compositions.
Accordingly, a primary object o~ this invention is to provide smoke suppressed flame retardant thermoset resin compositions.
., . , , . ; .
GL354.APP ~J ~3 ~J 3i~ 2~, A related object is to provide flame retardant unsaturated polyester resin compositions with a reduced tendency to smoke under burning conditions.
A further object is to provide unsaturated polyester resin compositions incorporating bicyclic phosphat~ compound and flame retardant agents.
SUMMARY OF T~E INVENTION
The foregoing and other object~, advantages and features of the present invention may be achievable with smoke suppressed thermoset resin compositions incorporating an additive mixture comprising a flame retardant agent and a bicyclic phosphate compound of the the followin~ Formula (I):
O _ - R
O=P ~ - CH
X
where X is OH, OR', or OC(O~R'; R i6 H or a saturated or unsaturated straight-chain or branched-chain Cl-C17 alkyl; and R' i8 a saturated or unsaturated straight-chain or branched chain Cl-C17 alkyl. The present invention is particularly useul with isophthalic un~aturated polyesters, orthophthalic unsaturated polyesters, vinylester resins, and epoxy resins. Compositions in accordance with this invention exhibit a reduced tendency to smoke under burning conditions.
. .: - . . .
- . . . . .
:, ;, ' . ;;' , ' ' , ~
GL354.APP
DESCRIPTION OF THE PREFERRED EMBODIMENTS
This invention relates to smoke suppressed flame retardant thermoset resin compositions. In pa:rticular, the invention relates to unsaturated polyesters, vinylester resins and epoxy resin compositions which are flame retardant and which exhibit a reduced tendency to smoke when burning. Compositions in accordance with this invention incorporate an additive mixture comprising one or more bicyclic phosphate compounds and one or more halogen-containing flame retardants.
Preferred bicyclic phosphates in accordance with this invention are compounds of Formula (I) where X is OH or OC(O)R'.
The most preferred bicyclic compounds are 2,6,7-trioxa-phosphobicyclo[2.2.2]-octane-4-methanol-1-oxide (Compound BCP, that is, Formula [I] when R is H and X is OH), and 2,6,7-trioxa-1-phosphobicyclo[2.2.2]-octane-4-methanol, acetate, 1-oxide (Compound BCP-A, that is, when R is H and X is OC(O)CH3).
The flame retardant agent employed in accordance with the present invention may be any common flame retardant agent which can be used to reduce the flammability of thermoset resins, ~uch as halogenated compounds containing bromine and chlorine, or inorganic materials, such as metal hydrates, metal borates, antimony-containing compounds, or phosphorous-containing compounds.
Preferred halogen-containing compounds are di(octyl)tetrabromophthalate, hexabromocyclododecane, tetrabromobisphenol A, te.trabromobisphenol A
bis-(dibromopropylether), dibromo(dibromoethyl)cyclohexane, .
.
GL354.APP
~ 3 2 ~
atrabromocyclooctane, bis-(dibromonorbornane dicarboximido)ethane, bis~(tetrabromopht~alimido)ethane, Diels-Alder adduct of chlorinated cyclopentadiene and unsaturated cycloaliphatic compound, bis-(tribromophenoxyethyl)-tetrabromobisphenol A ether, pentabromodiphenyl ether, octabromodiphenyl ether, decabromodiphenyl ether, bis-(tribromophenoxy)ethane, bis~(pentabromophenoxy)ethane, chloropentabromocyclohexane, (tribromophenoxy)-(dibromononylphenoxy)ethane, pentabromoethylbenzene, pentabromododecylbenzene, carbonate oligomers of tetrabromobisphenol A, poly(bromostyrene), and brominated polystyrene, poly(bromophenylene) ether, and mixtures thereof.
Substantially any suitable metal hydrates and oxides may be employed as flame retardant agents, including hydrates and oxides of aluminum, iron, zinc, magnesium, tin, molybdenum and antimony.
Alumina trihydrate, magnesium hydroxide, and antimony trioxide are the preferred compounds in this class.
Suitable metal boron-containing flame retardant compounds include zinc, barium, calcium, magnesium, cadmium and mercury.
Zinc borate is the preferred compound in this class.
Substantially any suitable phosphorus-containing compound may be used a~ a flame retardant agent, including ammonium polyphosphate, arylphosphates and alkarylphosphates.
Particularly preferred are alkaryl phosphates commercially .
.: : , . .
~, :
- :
, '~
:
GL354.APP
. 2 ~, ~vailable from FMC Corporation under the trademarks Kronitex lO0 and Santicizer 148.
The foregoing flame retardant compounds are added to thermo-plastic resins at levels such that the resultant resi~ composi-tion may be rendered flame retardant.
Thermoset resins which may be treated in accordance with the invention include thermosets such as polyesters, epoxies, vinylesters, alkyl polyesters, melamine isocyanurates, polyurethanes, phenolic resins and phenylene-based resins.
Isophthalic and orthophthalic unsaturated polyesters, vinylester resins and epoxY resins are preferred thermosets in accordance with this invention.
It is custo~ary to provide thermoset resins such as unsaturated polyesters with glass fiber reinforcements. Glass fiber reinforcements may usefully be employed at a level of about 5 to 60 percent by weight of the composition, preferably about 10 to 40 percent by weight.
The scope of the present invention also includes the incorporation of other additives in the composition so far as to produce a particular end result. Such additives include, without limitation, blowing ayents, heat stabilizers, light stabilizers, plasticizers, pigments, preservatives, ultraviolet light stabi-lizers, fillers, antioxidants, antistatic agents and other materials well known to those skilled in the art, for example, as described in Modern Plastics EncYclo~edia, Vol. 63, No. lOAJ
McGraw-Hill, Inc. (1986).
' ' ' ~ ~ .
: :
GL354.APP
The bicyclic phosphates of the present invention may be used alone or as mixtures of any such compounds. When mixtures of bicyclic phosphates are employed, substantially any combinations of amounts and proportions of the individual compounds may be used. The use of Compound BCP and Compound BCP-A is especially preferred in accordance with this invention.
The bicyclic phosphate may be employed at substantially any level because even very low levels are believed to assist in smoke suppression. Desirably, bicyclic phosphates are present at a level of about 1 to 30 percent, preferably about 5 to 25 percent, and most preferably about 10 to 20 percent, all by weight of the composition.
The flame retardant agents of the present invention may be used alone or as mixtures of any such compounds. When mixtures of flam~ agents are employed, ~ubstantially any combinations of amounts and proportions of the individual compounds may be used.
The use of di-(2-ethylhexyl)tetrabromophthalate, alumina trihydrate, magnesium hydroxide, zinc borate, antimony tioxide, and alkaryl phosphates are especially preerred in accordance with this invention. Preferably flame retardants are employed at a level of about 1 to 65 percent by weight of the composition, preferably about 5 to 45 percent, and most preferably about 30 to 40 percent, depending on the particular resin system and retardant employed.
Desirably, the bicyclic phosphate compound a~d flame retardant are provided as a mixture useful as an additive which may be added to the thermoset resin compositions. The additive ,, ,' ' ' ' ' ' ~ ~ .
' GL354.APP ~ J
mixture utilizes bicyclic phosphate and flame retardant in a weight ratio lying in the range of about 1:2S to 20:1, most preferably, about 3:20 to 20:3.
The additive mixture is incorporated into the polymer composition at a level such that the resulting resin composition is rendered flame retardant. In general, the additive mixture is provided in the flame retardant at a level of about 2 - 50 percent by weight of the resin composition, preferably about 3 -30 percent by weight.
Practice of the present invention is illustrated by the following examples, which are given to illustrate the invention and should not be construed as limiting its scope.
EXAMPLES
Pre~aration of Unsaturated Polyesters. Unsaturated polyesters ("UPE") thermosets were prepared by standard hand lay-up procedures. Koppers Dion 810 isophthalic unsaturated polyester resin was used in all cases. ~ncured resin was promoted with cobalt naphthenate, blended with fillers, additives, and glass reinforcing agent. The mixture was degased in a vacuum oven, treated with methyl ethyl ketone ("NEK") peroxide catalyst, and cured at room temperature for 12 hours followed by 1 hour at 100C. The general composition of the ~amples in parts by weight ("PBW") is given in the following chart.
.
. . .
' ~` :
GL354.APP
!
USPE Formulations __ _ Component PBW
Koppers Dion 810 varied Isophthalic Re sin Flame Retardant varied Chopped Strand Glass 20 TiO2 MEK Peroxide Cobalt Naphthenate 0.5 __ , _ _ _ _ The specific composition of each sample prepared using this methodology is given in Ta~le I. These samples were subjected to a series of standard ~est procedures as described below.
Flammability Test Procedures. The following test protocols were used for the samples prepared in the foregoing manner.
'' ' ' ' ' ,' ' , ' . ". " ~ ", . ~; ', ': ' ' '` ,, '' ~ .' ' '~ ' '' .
GL354.APP
-Test Method Description .
Four Foot Tunnel Test Apparatus to measure flame spread and smoke development in accordance with ASTM-E-84 test procedures.
The length of the specimen was four feet instead of 25 feet. Lower values for flame spread and smoke development indicate improved perfor.mance.
HLT-l Vertical Flame Test A test method which rankP specimen based on time to extinguish a flame after ignition. The highest rating (best performance) is 100.
Each of the test samples was subjected to these tests. The data are given in Table I.
.
; : . : ' `:: ' . ~ - :
, : , . . . : .
.
GL354.APP
TA LE I
NUMBER BCP TYPE AMOUNT FL.AMESMOKE ASTM BARCOL
wt % wt % SPREADDEVELOPMENT ASTM
2 15 MgOH 38 17 85 10045 COMP 2 0 MgOH 38 39 640 2447 3 15 ZnBor 38 19 120 g644 COMP 3 0 ZnBor 38 53 945 2448 BCP - Preferred bicyclic phosphate ATH - alumina trihydrate MgOH - magnesium hydroxide 2nBor - zinc borate These data demonstrate the patentability of the subject invention. The Control Example shows the effect of 15.0% BCP on flame spread and smoke development, as measured by the four foot tunnel testing for isophthalic polyester thermoset composites.
Comparative Examples 1-3 show the effect of various flame retardants on flammability performance when Compound BCP is not present. Examples 1-3 illustrate the invention using the same flame retardant agents in combination with Compound BCP.
In every case, compositions comprising Compound BCP had lower smoke development than the Control Example (a sy3tem without additional flame retardant agents) or the corresponding Comparative Examples 1-3 (i.e., systems without Compound BCP~.
Moreover, compositions containing BCP did not afect physical property performance, as exemplified by the minimal change in Hardness.
. . . ... , . . . -.
- , . . .: ~
' . i ~
,;
. , :
' 1,
Many prior art references describe the use of a variety of smoke additives in unsaturated polyesters. Modern Plastics Encyclopedia, Vol. 63, No. lOA, McGraw-Hill, Inc., pp. 179-180 (1986). However, the selection of a suitable smoXe suppressant for thermoset resins is not predictable. Selection is particu-larly difficult when flame retardants are employed, exacerbated by the complex interaction between the polymer and the flame retardant agent.
Hechenbleikner, et al. describe in U.S. Patent No. 3,293,327 the production of bicyclic phosphites, phosphonates, thiophosphates, and selenophosphates. These compositions are said to be stabilizers for vinyl halide resins. They are alleged to be useful as heat stabilizers for vinyl chloride resin, and as antioxidants for fats and oils. The Hechenbleikner patent does not specify the use of bicyclic phosphates to achieve low smoke thermoset resin compositions, nor does it disclose that cyclic phosphates of the present invention coul~ be used with flame retardant agents to produce smoke suppressed flame retardant thermoset compositions.
British Patent No. g99,793 ~escribes a process for producing organic phosphates by ~ubjecting organic phosphites to reaction with peracetic acid. This patent shows a method for producing the most preferred bicyclic phosphate of the present invention, 2,6,7-trioxa-l-phosphobicyclo~2.2.2]-octane-4-methanol-l-oxide and teaches the use of acetal ring-containing phosphates as plasticizers or functional fluids. The British patent, however, does not disclose the present invention. It does not mention ' ', :~,,, , ~
GL354.APP
2~ 3.~. 2 ~
~ yclic phosphates as being useful for flame retardant thermoset resins, nor that the most preferred bicyclic phosphate of the present invention can be used with flame retardant-additives to yield improved thermoset compositions.
Hills, et al. describe in U.S. Patent No. 3,873,496 a 1ame retardant polyester composition which contains 5 to 25 percent of a hydroxymethyl bicyclic phosphate compound as a ~lame retardant additive. Hills did not observe the ability for bicyclic phos-phates to act as smoke suppressors for thermoset resin compositions which employ other compounds as the primary flame retardant additive.
Halpern, e~ al. describe in U.S. Patent No. 4,341,694 a composition comprising 2,6,7-trioxa-1-phosphobicyclo[2.~.2]-octane-4-methanol-1-oxide and a nitrogen-containing co-additive, which are intumescent and are adaptable to flame retard polyolefins, polyvinylaromatic resins, polycarbonates, PVC and blends thereof. Halpern did not observe any smoke suppression of the present invention.
Parr, et al. describe in U.S. Patent No. 4,801,625 a flame resistant composition having (1) an organic polymeric substance in intimate contact with (2) a bicyclic phosphorous compound, and (3) a gas producing compound. Parr is silent on the use of bicyclic compounds to attain smoke suppressed flame retardant thermoset compositions.
Accordingly, a primary object o~ this invention is to provide smoke suppressed flame retardant thermoset resin compositions.
., . , , . ; .
GL354.APP ~J ~3 ~J 3i~ 2~, A related object is to provide flame retardant unsaturated polyester resin compositions with a reduced tendency to smoke under burning conditions.
A further object is to provide unsaturated polyester resin compositions incorporating bicyclic phosphat~ compound and flame retardant agents.
SUMMARY OF T~E INVENTION
The foregoing and other object~, advantages and features of the present invention may be achievable with smoke suppressed thermoset resin compositions incorporating an additive mixture comprising a flame retardant agent and a bicyclic phosphate compound of the the followin~ Formula (I):
O _ - R
O=P ~ - CH
X
where X is OH, OR', or OC(O~R'; R i6 H or a saturated or unsaturated straight-chain or branched-chain Cl-C17 alkyl; and R' i8 a saturated or unsaturated straight-chain or branched chain Cl-C17 alkyl. The present invention is particularly useul with isophthalic un~aturated polyesters, orthophthalic unsaturated polyesters, vinylester resins, and epoxy resins. Compositions in accordance with this invention exhibit a reduced tendency to smoke under burning conditions.
. .: - . . .
- . . . . .
:, ;, ' . ;;' , ' ' , ~
GL354.APP
DESCRIPTION OF THE PREFERRED EMBODIMENTS
This invention relates to smoke suppressed flame retardant thermoset resin compositions. In pa:rticular, the invention relates to unsaturated polyesters, vinylester resins and epoxy resin compositions which are flame retardant and which exhibit a reduced tendency to smoke when burning. Compositions in accordance with this invention incorporate an additive mixture comprising one or more bicyclic phosphate compounds and one or more halogen-containing flame retardants.
Preferred bicyclic phosphates in accordance with this invention are compounds of Formula (I) where X is OH or OC(O)R'.
The most preferred bicyclic compounds are 2,6,7-trioxa-phosphobicyclo[2.2.2]-octane-4-methanol-1-oxide (Compound BCP, that is, Formula [I] when R is H and X is OH), and 2,6,7-trioxa-1-phosphobicyclo[2.2.2]-octane-4-methanol, acetate, 1-oxide (Compound BCP-A, that is, when R is H and X is OC(O)CH3).
The flame retardant agent employed in accordance with the present invention may be any common flame retardant agent which can be used to reduce the flammability of thermoset resins, ~uch as halogenated compounds containing bromine and chlorine, or inorganic materials, such as metal hydrates, metal borates, antimony-containing compounds, or phosphorous-containing compounds.
Preferred halogen-containing compounds are di(octyl)tetrabromophthalate, hexabromocyclododecane, tetrabromobisphenol A, te.trabromobisphenol A
bis-(dibromopropylether), dibromo(dibromoethyl)cyclohexane, .
.
GL354.APP
~ 3 2 ~
atrabromocyclooctane, bis-(dibromonorbornane dicarboximido)ethane, bis~(tetrabromopht~alimido)ethane, Diels-Alder adduct of chlorinated cyclopentadiene and unsaturated cycloaliphatic compound, bis-(tribromophenoxyethyl)-tetrabromobisphenol A ether, pentabromodiphenyl ether, octabromodiphenyl ether, decabromodiphenyl ether, bis-(tribromophenoxy)ethane, bis~(pentabromophenoxy)ethane, chloropentabromocyclohexane, (tribromophenoxy)-(dibromononylphenoxy)ethane, pentabromoethylbenzene, pentabromododecylbenzene, carbonate oligomers of tetrabromobisphenol A, poly(bromostyrene), and brominated polystyrene, poly(bromophenylene) ether, and mixtures thereof.
Substantially any suitable metal hydrates and oxides may be employed as flame retardant agents, including hydrates and oxides of aluminum, iron, zinc, magnesium, tin, molybdenum and antimony.
Alumina trihydrate, magnesium hydroxide, and antimony trioxide are the preferred compounds in this class.
Suitable metal boron-containing flame retardant compounds include zinc, barium, calcium, magnesium, cadmium and mercury.
Zinc borate is the preferred compound in this class.
Substantially any suitable phosphorus-containing compound may be used a~ a flame retardant agent, including ammonium polyphosphate, arylphosphates and alkarylphosphates.
Particularly preferred are alkaryl phosphates commercially .
.: : , . .
~, :
- :
, '~
:
GL354.APP
. 2 ~, ~vailable from FMC Corporation under the trademarks Kronitex lO0 and Santicizer 148.
The foregoing flame retardant compounds are added to thermo-plastic resins at levels such that the resultant resi~ composi-tion may be rendered flame retardant.
Thermoset resins which may be treated in accordance with the invention include thermosets such as polyesters, epoxies, vinylesters, alkyl polyesters, melamine isocyanurates, polyurethanes, phenolic resins and phenylene-based resins.
Isophthalic and orthophthalic unsaturated polyesters, vinylester resins and epoxY resins are preferred thermosets in accordance with this invention.
It is custo~ary to provide thermoset resins such as unsaturated polyesters with glass fiber reinforcements. Glass fiber reinforcements may usefully be employed at a level of about 5 to 60 percent by weight of the composition, preferably about 10 to 40 percent by weight.
The scope of the present invention also includes the incorporation of other additives in the composition so far as to produce a particular end result. Such additives include, without limitation, blowing ayents, heat stabilizers, light stabilizers, plasticizers, pigments, preservatives, ultraviolet light stabi-lizers, fillers, antioxidants, antistatic agents and other materials well known to those skilled in the art, for example, as described in Modern Plastics EncYclo~edia, Vol. 63, No. lOAJ
McGraw-Hill, Inc. (1986).
' ' ' ~ ~ .
: :
GL354.APP
The bicyclic phosphates of the present invention may be used alone or as mixtures of any such compounds. When mixtures of bicyclic phosphates are employed, substantially any combinations of amounts and proportions of the individual compounds may be used. The use of Compound BCP and Compound BCP-A is especially preferred in accordance with this invention.
The bicyclic phosphate may be employed at substantially any level because even very low levels are believed to assist in smoke suppression. Desirably, bicyclic phosphates are present at a level of about 1 to 30 percent, preferably about 5 to 25 percent, and most preferably about 10 to 20 percent, all by weight of the composition.
The flame retardant agents of the present invention may be used alone or as mixtures of any such compounds. When mixtures of flam~ agents are employed, ~ubstantially any combinations of amounts and proportions of the individual compounds may be used.
The use of di-(2-ethylhexyl)tetrabromophthalate, alumina trihydrate, magnesium hydroxide, zinc borate, antimony tioxide, and alkaryl phosphates are especially preerred in accordance with this invention. Preferably flame retardants are employed at a level of about 1 to 65 percent by weight of the composition, preferably about 5 to 45 percent, and most preferably about 30 to 40 percent, depending on the particular resin system and retardant employed.
Desirably, the bicyclic phosphate compound a~d flame retardant are provided as a mixture useful as an additive which may be added to the thermoset resin compositions. The additive ,, ,' ' ' ' ' ' ~ ~ .
' GL354.APP ~ J
mixture utilizes bicyclic phosphate and flame retardant in a weight ratio lying in the range of about 1:2S to 20:1, most preferably, about 3:20 to 20:3.
The additive mixture is incorporated into the polymer composition at a level such that the resulting resin composition is rendered flame retardant. In general, the additive mixture is provided in the flame retardant at a level of about 2 - 50 percent by weight of the resin composition, preferably about 3 -30 percent by weight.
Practice of the present invention is illustrated by the following examples, which are given to illustrate the invention and should not be construed as limiting its scope.
EXAMPLES
Pre~aration of Unsaturated Polyesters. Unsaturated polyesters ("UPE") thermosets were prepared by standard hand lay-up procedures. Koppers Dion 810 isophthalic unsaturated polyester resin was used in all cases. ~ncured resin was promoted with cobalt naphthenate, blended with fillers, additives, and glass reinforcing agent. The mixture was degased in a vacuum oven, treated with methyl ethyl ketone ("NEK") peroxide catalyst, and cured at room temperature for 12 hours followed by 1 hour at 100C. The general composition of the ~amples in parts by weight ("PBW") is given in the following chart.
.
. . .
' ~` :
GL354.APP
!
USPE Formulations __ _ Component PBW
Koppers Dion 810 varied Isophthalic Re sin Flame Retardant varied Chopped Strand Glass 20 TiO2 MEK Peroxide Cobalt Naphthenate 0.5 __ , _ _ _ _ The specific composition of each sample prepared using this methodology is given in Ta~le I. These samples were subjected to a series of standard ~est procedures as described below.
Flammability Test Procedures. The following test protocols were used for the samples prepared in the foregoing manner.
'' ' ' ' ' ,' ' , ' . ". " ~ ", . ~; ', ': ' ' '` ,, '' ~ .' ' '~ ' '' .
GL354.APP
-Test Method Description .
Four Foot Tunnel Test Apparatus to measure flame spread and smoke development in accordance with ASTM-E-84 test procedures.
The length of the specimen was four feet instead of 25 feet. Lower values for flame spread and smoke development indicate improved perfor.mance.
HLT-l Vertical Flame Test A test method which rankP specimen based on time to extinguish a flame after ignition. The highest rating (best performance) is 100.
Each of the test samples was subjected to these tests. The data are given in Table I.
.
; : . : ' `:: ' . ~ - :
, : , . . . : .
.
GL354.APP
TA LE I
NUMBER BCP TYPE AMOUNT FL.AMESMOKE ASTM BARCOL
wt % wt % SPREADDEVELOPMENT ASTM
2 15 MgOH 38 17 85 10045 COMP 2 0 MgOH 38 39 640 2447 3 15 ZnBor 38 19 120 g644 COMP 3 0 ZnBor 38 53 945 2448 BCP - Preferred bicyclic phosphate ATH - alumina trihydrate MgOH - magnesium hydroxide 2nBor - zinc borate These data demonstrate the patentability of the subject invention. The Control Example shows the effect of 15.0% BCP on flame spread and smoke development, as measured by the four foot tunnel testing for isophthalic polyester thermoset composites.
Comparative Examples 1-3 show the effect of various flame retardants on flammability performance when Compound BCP is not present. Examples 1-3 illustrate the invention using the same flame retardant agents in combination with Compound BCP.
In every case, compositions comprising Compound BCP had lower smoke development than the Control Example (a sy3tem without additional flame retardant agents) or the corresponding Comparative Examples 1-3 (i.e., systems without Compound BCP~.
Moreover, compositions containing BCP did not afect physical property performance, as exemplified by the minimal change in Hardness.
. . . ... , . . . -.
- , . . .: ~
' . i ~
,;
. , :
' 1,
Claims (15)
1. A smoke suppressed thermoset resin composition comprising a thermoset resin and a mixture comprising:
at least one flame retardant agent; and at least one bicyclic phosphate compound of the formula:
where X is OH, OR', or OC(O)R'; R is H or a saturated or unsaturated straight-chain or branched-chain C1-C17 alkyl; and R' is a saturated or unsaturated straight-chain or branched-chain C1-C17 alkyl.
at least one flame retardant agent; and at least one bicyclic phosphate compound of the formula:
where X is OH, OR', or OC(O)R'; R is H or a saturated or unsaturated straight-chain or branched-chain C1-C17 alkyl; and R' is a saturated or unsaturated straight-chain or branched-chain C1-C17 alkyl.
2. A composition, as claimed in claim 1, wherein the flame retardant agent is a member selected from the group consisting of halogenated compounds, metal hydrates, metal borates, phosphorous compounds, and mixtures thereof.
3. A composition, as claimed in claim 1, wherein the flame retardant agent is a member selected from the group consisting of alumina trihydrate, magnesium hydroxide, antimony trioxide, zinc borate and alkaryl phosphates.
4. A composition, as claimed in claim 1, wherein the bicyclic phosphate compound is 2,6,7-trioxa-phosphobicyclo [2.2.2]-octane-4-methanol-1-oxide; or 2,6,7-trioxa-1-phosphobicyclo[2.2.2]-octane-4-methanol, acetate, 1-oxide.
GL354.APP
GL354.APP
5. A composition, as claimed in claim 1, wherein the resin is a member selected from the group consisting of isophthalic unsaturated polyesters, orthophthalic unsaturated polyesters, vinylester resins and epoxy resins.
6. A composition, as claimed in claim 4, wherein the member is an unsaturated polyester.
7. A composition, as claimed in claim 1, wherein the weight ratio of bicyclic phosphate compound to flame retardant agent lies in the range of about 1:25 to 20:1.
8. A composition, as claimed in claim 1, wherein the mixture of bicyclic phosphate compound and flame retardant agent is provided in the resin composition at a level lying in the range of about 2 - 50 percent by weight of the overall composition.
9. A composition, as claimed in claim 8, wherein the composition additionally comprises glass fiber reinforcements.
10. A method for suppressing the tendency of thermoset resin compositions to smoke under conditions of burning comprising the step of incorporating therein an effective amount of a mixture comprising:
a flame retardant agent; and a bicyclic phosphate compound of the formula:
GL354.APP
where X is OH, OR', or OC(O)R'; R is H or a saturated or unsaturated straight-chain or branched-chain C1-C17 alkyl; and R' is a saturated or unsaturated straight-chain or branched-chain C1-C17 alkyl.
a flame retardant agent; and a bicyclic phosphate compound of the formula:
GL354.APP
where X is OH, OR', or OC(O)R'; R is H or a saturated or unsaturated straight-chain or branched-chain C1-C17 alkyl; and R' is a saturated or unsaturated straight-chain or branched-chain C1-C17 alkyl.
11. A method, as claimed in claim 10, wherein the flame retardant agent is a member selected from the group consisting of halogenated compounds, metal hydrates, metal borates, phosphorous compounds, and mixtures thereof.
12. A method, as claimed in claim 10, wherein the flame retardant agent is a member selected from the group consisting of alumina trihydrate, magnesium hydroxide, antimony trioxide, zinc borate, and alkaryl phosphate.
13. A method, as claimed in claim 10, wherein the bicyclic phosphate compound is 2,6,7-trioxa-phosphobicyclo [2.2.2]-octane-4-methanol-1-oxide; or 2,6,7-trioxa-1-phosphobicyclo[2.2.2]-octane-4-methanol, acetate, 1-oxide.
14. A method, as claimed in claim 10, wherein the weight ratio of bicyclic phosphate compound to halogen-containing flame retardant lies in the range of about 1:25 to 20:1.
15. A method, where the thermoset resin composition additionally comprises glass fiber reinforcements.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US40814389A | 1989-09-15 | 1989-09-15 | |
US408,143 | 1989-09-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2025122A1 true CA2025122A1 (en) | 1991-03-16 |
Family
ID=23615031
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002025122A Abandoned CA2025122A1 (en) | 1989-09-15 | 1990-09-12 | Smoke suppressed flame retardant unsaturated polyester resin compositions |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0491870A1 (en) |
JP (1) | JPH05501423A (en) |
KR (1) | KR927003726A (en) |
AU (1) | AU640959B2 (en) |
CA (1) | CA2025122A1 (en) |
IL (1) | IL95674A (en) |
WO (1) | WO1991004295A2 (en) |
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EP2921498A1 (en) | 2014-03-17 | 2015-09-23 | Eidgenössische Materialprüfungs- und Forschungsanstalt EMPA | Dopo-based hybrid flame retardants |
WO2021193883A1 (en) * | 2020-03-25 | 2021-09-30 | 株式会社Adeka | Flame retardant composition, flame-retardant synthetic-resin composition, and molded object |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US3189633A (en) * | 1960-09-20 | 1965-06-15 | Pittsburgh Plate Glass Co | 2, 6, 7-trioxa-1-phosphabicyclo [2.2.2] octane sulfo-oxo, and seleno derivatives and process for making same |
US4734455A (en) * | 1986-12-05 | 1988-03-29 | The Dow Chemical Company | Stabilizers for filled polyol compositions |
US4992215A (en) * | 1988-10-31 | 1991-02-12 | Tag Investments, Inc. | Polymer fire retardant |
AU640705B2 (en) * | 1990-10-31 | 1993-09-02 | Sumitomo Rubber Industries, Ltd. | Apparatus for forming ring-shaped member |
-
1990
- 1990-09-12 AU AU65305/90A patent/AU640959B2/en not_active Ceased
- 1990-09-12 WO PCT/US1990/005158 patent/WO1991004295A2/en not_active Application Discontinuation
- 1990-09-12 EP EP90915264A patent/EP0491870A1/en not_active Withdrawn
- 1990-09-12 KR KR1019920700582A patent/KR927003726A/en not_active Application Discontinuation
- 1990-09-12 JP JP2514172A patent/JPH05501423A/en active Pending
- 1990-09-12 CA CA002025122A patent/CA2025122A1/en not_active Abandoned
- 1990-09-13 IL IL9567490A patent/IL95674A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
WO1991004295A2 (en) | 1991-04-04 |
EP0491870A1 (en) | 1992-07-01 |
WO1991004295A3 (en) | 1991-05-16 |
JPH05501423A (en) | 1993-03-18 |
IL95674A (en) | 1995-05-26 |
AU640959B2 (en) | 1993-09-09 |
AU6530590A (en) | 1991-04-18 |
IL95674A0 (en) | 1991-06-30 |
KR927003726A (en) | 1992-12-18 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Discontinued |