EP0500608A1 - Smoke suppressed flame retardant thermoplastic resin compositions - Google Patents
Smoke suppressed flame retardant thermoplastic resin compositionsInfo
- Publication number
- EP0500608A1 EP0500608A1 EP19900916156 EP90916156A EP0500608A1 EP 0500608 A1 EP0500608 A1 EP 0500608A1 EP 19900916156 EP19900916156 EP 19900916156 EP 90916156 A EP90916156 A EP 90916156A EP 0500608 A1 EP0500608 A1 EP 0500608A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- flame retardant
- composition
- retardant agent
- chain
- 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.)
- Withdrawn
Links
- 239000000779 smoke Substances 0.000 title claims abstract description 29
- 239000011342 resin composition Substances 0.000 title claims abstract description 15
- 229920005992 thermoplastic resin Polymers 0.000 title claims abstract description 12
- 239000003063 flame retardant Substances 0.000 title abstract description 35
- 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 abstract description 31
- 239000000203 mixture Substances 0.000 claims abstract description 54
- -1 bicyclic phosphate compounds Chemical class 0.000 claims abstract description 34
- 229920005989 resin Polymers 0.000 claims abstract description 11
- 239000011347 resin Substances 0.000 claims abstract description 11
- 239000004793 Polystyrene Substances 0.000 claims abstract description 9
- 229920002223 polystyrene Polymers 0.000 claims abstract description 8
- 229920001291 polyvinyl halide Polymers 0.000 claims abstract description 7
- 229910019142 PO4 Inorganic materials 0.000 claims description 28
- 150000001875 compounds Chemical class 0.000 claims description 26
- 239000012757 flame retardant agent Substances 0.000 claims description 21
- 239000010452 phosphate Substances 0.000 claims description 19
- 239000004800 polyvinyl chloride Substances 0.000 claims description 16
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 16
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Chemical class 0.000 claims description 8
- 238000000034 method Methods 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
- 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 claims description 5
- 150000004677 hydrates Chemical class 0.000 claims description 5
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical class [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 5
- 239000000347 magnesium hydroxide Substances 0.000 claims description 5
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 5
- 229920005672 polyolefin resin Polymers 0.000 claims description 5
- 229920005990 polystyrene resin Polymers 0.000 claims description 5
- 150000004684 trihydrates Chemical class 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 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
- 229910052787 antimony Inorganic materials 0.000 claims description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 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 2
- 239000004698 Polyethylene Substances 0.000 claims description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 229920001748 polybutylene Polymers 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 claims 1
- 150000001463 antimony compounds Chemical class 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 1
- 229920000098 polyolefin Polymers 0.000 abstract description 6
- 238000002485 combustion reaction Methods 0.000 abstract description 3
- 235000021317 phosphate Nutrition 0.000 description 21
- 239000000654 additive Substances 0.000 description 17
- 229920001169 thermoplastic Polymers 0.000 description 12
- 239000004416 thermosoftening plastic Substances 0.000 description 12
- 125000002619 bicyclic group Chemical group 0.000 description 10
- 230000000996 additive effect Effects 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000004014 plasticizer Substances 0.000 description 6
- 238000009472 formulation Methods 0.000 description 4
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920000642 polymer Polymers 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
- 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 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-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
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- JJXNVYMIYBNZQX-UHFFFAOYSA-N diphenyl (2-propan-2-ylphenyl) phosphate Chemical compound CC(C)C1=CC=CC=C1OP(=O)(OC=1C=CC=CC=1)OC1=CC=CC=C1 JJXNVYMIYBNZQX-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- 238000010348 incorporation Methods 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
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 238000010998 test method Methods 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
- YHMOQCYOOUHZSF-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-[1-(2,3,4,5,6-pentabromophenoxy)ethoxy]benzene Chemical compound BrC=1C(Br)=C(Br)C(Br)=C(Br)C=1OC(C)OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br YHMOQCYOOUHZSF-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
- LXIZRZRTWSDLKK-UHFFFAOYSA-N 1,3-dibromo-5-[2-[3,5-dibromo-4-(2,3-dibromopropoxy)phenyl]propan-2-yl]-2-(2,3-dibromopropoxy)benzene Chemical compound C=1C(Br)=C(OCC(Br)CBr)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(OCC(Br)CBr)C(Br)=C1 LXIZRZRTWSDLKK-UHFFFAOYSA-N 0.000 description 1
- NEUHYMIDXNTABG-UHFFFAOYSA-N 4,5,6,7-tetrabromo-2-[1-(4,5,6,7-tetrabromo-1,3-dioxoisoindol-2-yl)ethyl]isoindole-1,3-dione Chemical compound O=C1C(C(=C(Br)C(Br)=C2Br)Br)=C2C(=O)N1C(C)N1C(=O)C(C(Br)=C(Br)C(Br)=C2Br)=C2C1=O NEUHYMIDXNTABG-UHFFFAOYSA-N 0.000 description 1
- 239000004114 Ammonium polyphosphate Substances 0.000 description 1
- 239000004604 Blowing Agent 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
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-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
- 229910018316 SbOx Inorganic materials 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
- QRSFFHRCBYCWBS-UHFFFAOYSA-N [O].[O] Chemical compound [O].[O] QRSFFHRCBYCWBS-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
- 229920001276 ammonium polyphosphate Polymers 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 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
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000001246 bromo group Chemical group Br* 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
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 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
- 239000003925 fat Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000012796 inorganic flame retardant Substances 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
- 239000007788 liquid Substances 0.000 description 1
- UNYOJUYSNFGNDV-UHFFFAOYSA-M magnesium monohydroxide Chemical compound [Mg]O UNYOJUYSNFGNDV-UHFFFAOYSA-M 0.000 description 1
- 238000005259 measurement Methods 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
- 210000000056 organ Anatomy 0.000 description 1
- LPLPPIFARDQDDL-UHFFFAOYSA-N phenyl (2-propan-2-ylphenyl) hydrogen phosphate Chemical compound CC(C)C1=CC=CC=C1OP(O)(=O)OC1=CC=CC=C1 LPLPPIFARDQDDL-UHFFFAOYSA-N 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 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
- 229920000728 polyester Polymers 0.000 description 1
- 229920006216 polyvinyl aromatic Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent 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
Definitions
- thermoplastic resin compositions that exhibit a reduc tendency to generate smoke under burning conditions. More particularly, this invention relates to thermoplastic compositions such as polyvinyl chloride (“PVC"), polystyrene an polyolefins, comprising bicyclic phosphate compound(s); and fla retardant agent(s).
- PVC polyvinyl chloride
- polystyrene an polyolefins
- the compositions produced in accordance wi this invention exhibit a reduced tendency to smoke under burnin conditions.
- thermoplastics such as polystyrene, polyolefins, and polyvinyl halides
- Typical flame retardant agents include reactive or additive halogenated organ compounds, inorganic fillers, and special formulations based on phosphorous and ammonium salts.
- thermoplastic compositions Although efficient in suppressing the rate of combustion i a resin system, most flame retardants tend to affect adversely one or more key properties of the resin. For example, many fla retardant additives are ineffective at producing low smoke ("smoke suppressed") formulations. Recent public awareness about risk and hazard assessment during fire situations, and technical limitations of conventi flame retardant additives warrant a need for improved flame retardant thermoplastic compositions. In particular, a need exists for a thermoplastic composition that passes flammabili standards with low smoke and combustion by-product formation, does not detract from overall polymer performance.
- Hechenbleikner, et al. describe in U.S. Patent No. 3,293, the production of bicyclic phosphites, phosphonates, thiophosphates, and selenophosphates. These compositions are said to be stabilizers for vinyl halide resins. They are all to be useful as heat stabilizers for vinyl chloride resin, an antioxidants for fats and oils.
- the Hechenbleikner patent do not specify the use of bicyclic phosphates to achieve low smo thermoplastic resin compositions, nor does it disclose that cyclic phosphates of the present invention could be used with flame retardant agents to produce smoke suppressed flame retardant thermoplastic compositions.
- Halpern, et al. describe in U.S. Patent No. 4,341,694 a composition comprising 2,6,7-trioxa-l-phosphobicyclo[2.2.2]- octane-4-methanol-l-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 the present invention. ___
- Parr, et al. describe in U.S. Patent No. 4,801,625 a f resistant composition having (1) an organic polymeric subst in intimate contact with (2) a bicyclic phosphorous compoun (3) a gas producing compound. Parr is silent on the use of bicyclic compounds to attain smoke suppressed flame retarda thermoplastic compositions.
- a primary object of this invention is to provide smoke suppressed flame retardant thermoplastic compositions.
- a related object is to provide flame retardant thermopl polyvinyl chloride compositions with a reduced tendency to ⁇ under burning conditions.
- a further object is to provide polyvinyl chloride resin compositions incorporating bicyclic phosphate compound and flame retardants.
- thermoplastic polyvinyl halide, polyolefin or polystyrene resin compositions incorporating an effective amount of an additive mixture comprising a flame retardant agent and a bicyclic phosphate compound of the following Formula (I):
- compositions in accordance with this invention exhibit a reduced tendency to smoke under burning conditions.
- DESCRIPTION OF THE PREFERRED EMBODIMENTS This invention relates to smoke suppressed flame retardant thermoplastic polyvinyl halide, polyolefin and polystyrene compositions.
- thermoplastic polyvinyl chloride, polyolefin and polystyrene 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 flame retardant agents.
- Preferred bicyclic phosphates in accordance with this invention are compounds of Formula (I) where X is OH or OC(0)R' .
- the most preferred bicyclic compounds are 2,6,7-trioxa- phosphobicyclo[2.2.2]-octane-4-methanol-l-oxide (Compound BCP, that is, Formula [I] when R is H and X is OH), and 2,6,7-trioxa-l-phosphobicyclo[2.2.2]-octane-4-methanol, acetate, 1-oxide (Compound BCP-A, that is, when R is H and X is OC(0)CH 3 ).
- 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 thermoplastic resins, such as halogenated compounds containing bromine and/or chlorine, or inorganic materials, such as metal hydrates, metal borates, antimony-containing compounds, or phosphorous-containing compounds.
- Preferred halogen-containing compounds are di-(2-ethylhexyl)tetrabromophthalate, hexabromocyclododecane, tetrabromobisphenol A, tetrabromobisphenol A bis-(dibromopropylether), dibromo(dibromoethyl)cyclohexane, tetrabromocyclooctane, bis-(dibromonorbornane dicarboximido)ethane, bis-(tetrabromophthalimido)ethane, Diels-Alder adduct of chlorinated cyclopentadiene and an unsaturated cycloaliphatic compound, bis-(tribromophenoxyethyl) -tetrabromobisphenol A ether, pentabromodiphenyl ether, octabromodiphenyl ether, decabromodiphenyl
- any suitable metal hydrates and oxides may employed as flame retardant agents, including hydrates and oxi of aluminum, iron, zinc, magnesium, tin, molybdenum and antimo 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.
- any suitable phosphorus-containing compound may be used as a flame retardant agent, including ammonium polyphosphate, arylphosphates, alkarylphosphates and alkylphosphates. Particularly preferred are phenyl isopropylphenyl phosphate and isodecyldiphenyl phosphate commercially available from FMC Corporation under the trademar Kronitex 100 and Santicizer 148.
- the foregoing flame retardant compounds are added to ther plastic resins at effective levels such that the resultant res composition may be rendered flame retardant.
- thermoplastic resins which may be treated in accordance the invention include thermoplastics such as polyvinyl halid polystyrene, and homopolymers and copolymers of polypropylen polyethylene, and polybutylene.
- Polyvinyl chloride is most preferred in accordance with this invention.
- the scope of the present invention also includes the incorporation of other additives in the composition so far a produce a particular end result.
- additives include, wi limitation, blowing agents, heat stabilizers, light stabiliz plasticizers, pigments, preservatives, ultraviolet light sta lizers, fillers, antioxidants, antistatic agents and other materials well known to those skilled in the art, for example described in Modern Plastics Encyclopedia, Vol. j53_, No. 10A, McGraw-Hill, Inc. (1986).
- bicyclic phosphates of the present invention may be alone or as mixtures of any such compounds. When mixtures of bicyclic phosphates are employed, substantially any combinati of amounts and proportions of the individual compounds may be used.
- the use of Compound BCP and Compound BCP-A is especial preferred in accordance with this invention.
- the bicyclic phosphate may be employed at substantially level because even very low levels are believed to assist in smoke suppression. Preferably it is present at a level of at least 2 percent and preferably about 3 percent up to about 20 percent by weight of the composition.
- the flame retardant agents of the present invention may b used alone or as mixtures of any such compounds. When mixture of flame agents are employed, substantially any combinations o amounts and proportions of the individual compounds may be use.
- the use of di-(2-ethylhexyl)- tetrabromophthalate, alumina trihydrate, magnesium hydroxide, zinc borate, antimony trioxid and alkylaryl phosphates are especially preferred in accordanc with this invention.
- flame retardants are employed at a level of ab 2 to 50 percent by weight of the composition, preferably about to 20 percent, depending on the specific flame retardant and thermoplastic resin employed. Operative and preferred ranges various flame retardants in accordance with this invention are given in the Table I.
- BrFr - di-(2-ethylhexyl)tetrabromophthalides brominated flame retardant AAP - alkylarylphosphate (Kronitex 100 - FMC Corp.) ATH - alumina trihydrate MgOH - magnesium hydroxide ZnBor - zinc borate SbOx - antimony oxide
- the bicyclic phosphate compound and flame retardant are provided as a mixture useful as an additive which may be added to polystyrene or polyolefin resin compositions.
- the additive mixture utilizes bicyclic phosphate and flame retardant in a weight ratio lying in the range of about 1:25 to 20:1, most preferably, about 3:20 to 20:3.
- the additive mixture is incorporated into the polymer composition at an effective level such that the resulting resin composition is rendered flame retardant.
- 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.
- PVC polyvinylchloride
- powdered additives and flame retardant were blended a mixing bowl and warmed to 90°C.
- Liquid plasticizer was added and the admixture was compounded on a two-roll mill at 160°C.
- the compounded PVC material was compression molded at 180°C.
- Table II shows examples of the use of Compound BCP in flexible PVC formulations.
- the general formulation used is as follows: Material % by weight
- Dioctylphthalate Plasticizer varied (see below) Epoxidized Soya Plasticizer 5
- DOP dioctyl phthalate
- Control Example shows the effect of 5.0% BCP alone on the smoke performance of a 30 01 flexible PVC composition.
- Comparative Examples 2-6 show the effect of various flame retardants on smoke performance when Compound BCP is not present.
- Example 1 illustrates the invention when the flame retardant is a bromine-containing flame retardant.
- Example 2 illustrates the invention when the flame retardant is phosphate-containing flame retardant (an alkarylphosphate) .
- Example 3-5 illustrate the invention when the flame retardant is an inorganic flame retardant.
- compositions comprising a bicyclic phosphate (Compound BCP) and a flame retardant had lower smoke than the Control (i.e., a system without any additional flame retardant agent) or the corresponding Comparative Examples 2-6 (i.e., a system without bicyclic phosphate).
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Abstract
Les compositions de résines thermoplastiques ignifuges sans fumée comprennent un ou plusieurs composés de phosphates bicycliques, un ou plusieurs agents ignifuges ainsi que des résines d'halogénure de polyvinyle de polyoléfine ou de polystyrène. Ces compositions présentent une tendance réduite à fumer dans des conditions de combustion.Smokeless flame retardant thermoplastic resin compositions include one or more bicyclic phosphate compounds, one or more flame retardants as well as polyolefin or polystyrene polyvinyl halide resins. These compositions exhibit a reduced tendency to smoke under combustion conditions.
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40814289A | 1989-09-15 | 1989-09-15 | |
| US408142 | 1989-09-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0500608A1 true EP0500608A1 (en) | 1992-09-02 |
Family
ID=23615027
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19900916156 Withdrawn EP0500608A1 (en) | 1989-09-15 | 1990-09-12 | Smoke suppressed flame retardant thermoplastic resin compositions |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0500608A1 (en) |
| JP (1) | JPH05500983A (en) |
| KR (1) | KR927003711A (en) |
| AU (2) | AU6625390A (en) |
| CA (1) | CA2025172A1 (en) |
| IL (1) | IL95673A (en) |
| WO (1) | WO1991004294A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997041173A1 (en) * | 1996-04-26 | 1997-11-06 | Akzo Nobel N.V. | Flame retardant composition for polymers |
| US10851228B2 (en) | 2018-07-26 | 2020-12-01 | FSIT Services LLC | Flame-retardant composition |
| CN110894331B (en) * | 2019-12-19 | 2022-04-08 | 天津金发新材料有限公司 | Environment-friendly low-smoke flame-retardant HIPS material and preparation method thereof |
| CN115340736B (en) * | 2022-05-20 | 2023-09-29 | 扬州实嘉电缆材料有限公司 | Nitrogen-phosphorus flame retardant modified polyvinyl chloride fireproof cable material |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4341694A (en) * | 1981-07-06 | 1982-07-27 | Borg-Warner Corporation | Intumescent flame retardant compositions |
| US4801625A (en) * | 1987-08-27 | 1989-01-31 | Akzo America Inc. | Bicyclic phosphate ether, ester, and carbonate intumescent flame retardant compositions |
| KR910700007A (en) * | 1988-12-22 | 1991-03-13 | 윌리암 피. 블레이크 | Stable flame retardant and thermoplastic polyolefin and polystyrene compositions against heat and light |
-
1990
- 1990-09-12 KR KR1019920700594A patent/KR927003711A/en not_active Ceased
- 1990-09-12 AU AU66253/90A patent/AU6625390A/en not_active Abandoned
- 1990-09-12 CA CA002025172A patent/CA2025172A1/en not_active Abandoned
- 1990-09-12 EP EP19900916156 patent/EP0500608A1/en not_active Withdrawn
- 1990-09-12 JP JP2514943A patent/JPH05500983A/en active Pending
- 1990-09-12 WO PCT/US1990/005147 patent/WO1991004294A1/en not_active Ceased
- 1990-09-13 IL IL9567390A patent/IL95673A/en not_active IP Right Cessation
-
1994
- 1994-08-18 AU AU70355/94A patent/AU7035594A/en not_active Abandoned
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9104294A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| IL95673A0 (en) | 1991-06-30 |
| WO1991004294A1 (en) | 1991-04-04 |
| CA2025172A1 (en) | 1991-03-16 |
| IL95673A (en) | 1995-05-26 |
| AU6625390A (en) | 1991-04-18 |
| JPH05500983A (en) | 1993-02-25 |
| AU7035594A (en) | 1994-11-03 |
| KR927003711A (en) | 1992-12-18 |
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