US20030216484A1 - Blends of (alkyl substituted) triaryl phosphate esters with phosphorus-containing flame retardants for polyurethane foams - Google Patents
Blends of (alkyl substituted) triaryl phosphate esters with phosphorus-containing flame retardants for polyurethane foams Download PDFInfo
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- US20030216484A1 US20030216484A1 US10/441,573 US44157303A US2003216484A1 US 20030216484 A1 US20030216484 A1 US 20030216484A1 US 44157303 A US44157303 A US 44157303A US 2003216484 A1 US2003216484 A1 US 2003216484A1
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- United States
- Prior art keywords
- flame retardant
- phosphorus
- phosphate
- alkyl substituted
- triaryl
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 132
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims abstract description 84
- 229910052698 phosphorus Inorganic materials 0.000 title claims abstract description 84
- 239000011574 phosphorus Substances 0.000 title claims abstract description 84
- 239000000203 mixture Substances 0.000 title claims abstract description 65
- 125000000217 alkyl group Chemical group 0.000 title claims abstract description 47
- 229920005830 Polyurethane Foam Polymers 0.000 title claims abstract description 34
- 239000011496 polyurethane foam Substances 0.000 title claims abstract description 34
- 150000003014 phosphoric acid esters Chemical class 0.000 title description 15
- 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 123
- 239000000654 additive Substances 0.000 claims abstract description 53
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 52
- 239000010452 phosphate Substances 0.000 claims abstract description 44
- -1 phosphate ester Chemical class 0.000 claims abstract description 40
- 239000011541 reaction mixture Substances 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 12
- 230000000979 retarding effect Effects 0.000 claims abstract description 5
- 235000021317 phosphate Nutrition 0.000 claims description 49
- 230000000996 additive effect Effects 0.000 claims description 38
- 229920002635 polyurethane Polymers 0.000 claims description 33
- 239000004814 polyurethane Substances 0.000 claims description 33
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical class C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 claims description 30
- 229920005862 polyol Polymers 0.000 claims description 24
- 150000003077 polyols Chemical class 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 20
- OWICEWMBIBPFAH-UHFFFAOYSA-N (3-diphenoxyphosphoryloxyphenyl) diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=C(OP(=O)(OC=2C=CC=CC=2)OC=2C=CC=CC=2)C=CC=1)(=O)OC1=CC=CC=C1 OWICEWMBIBPFAH-UHFFFAOYSA-N 0.000 claims description 16
- HRKAMJBPFPHCSD-UHFFFAOYSA-N Tri-isobutylphosphate Chemical compound CC(C)COP(=O)(OCC(C)C)OCC(C)C HRKAMJBPFPHCSD-UHFFFAOYSA-N 0.000 claims description 11
- 239000012948 isocyanate Substances 0.000 claims description 11
- 150000002513 isocyanates Chemical class 0.000 claims description 11
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 9
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 claims description 9
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 6
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 claims description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
- YWDFOLFVOVCBIU-UHFFFAOYSA-N 1-dimethoxyphosphorylpropane Chemical compound CCCP(=O)(OC)OC YWDFOLFVOVCBIU-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 5
- GTVWRXDRKAHEAD-UHFFFAOYSA-N Tris(2-ethylhexyl) phosphate Chemical compound CCCCC(CC)COP(=O)(OCC(CC)CCCC)OCC(CC)CCCC GTVWRXDRKAHEAD-UHFFFAOYSA-N 0.000 claims description 5
- VONWDASPFIQPDY-UHFFFAOYSA-N dimethyl methylphosphonate Chemical compound COP(C)(=O)OC VONWDASPFIQPDY-UHFFFAOYSA-N 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 2
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims 4
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims 4
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 4
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 14
- 239000006260 foam Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- ISNNXHQBIBWQHG-UHFFFAOYSA-N CC.CC.CC.O=P(Oc1ccccc1)(Oc1ccccc1)Oc1ccccc1 Chemical compound CC.CC.CC.O=P(Oc1ccccc1)(Oc1ccccc1)Oc1ccccc1 ISNNXHQBIBWQHG-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011280 coal tar Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000012757 flame retardant agent Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000012974 tin catalyst Substances 0.000 description 2
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- ASMQGLCHMVWBQR-UHFFFAOYSA-M diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-M 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000006353 environmental stress Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000006261 foam material Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000582 polyisocyanurate Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
-
- 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
- C08K5/523—Esters of phosphoric acids, e.g. of H3PO4 with hydroxyaryl compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
-
- 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
-
- 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
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5313—Phosphinic compounds, e.g. R2=P(:O)OR'
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2110/00—Foam properties
- C08G2110/0008—Foam properties flexible
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2110/00—Foam properties
- C08G2110/0041—Foam properties having specified density
- C08G2110/005—< 50kg/m3
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2110/00—Foam properties
- C08G2110/0083—Foam properties prepared using water as the sole blowing agent
-
- 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
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
Definitions
- the present invention relates to flame retardant polyurethane compositions, and more particularly to flame retardant flexible polyurethane foam compositions, methods of flame retarding flexible polyurethane foam compositions, articles made therefrom and flame retardants that comprise blends of alkylated triaryl phosphate esters and phosphorus-containing flame retardant additives.
- Flame retardant additives commonly used in flexible polyurethane foams typically contain halogens. Non-halogen flame retardant additives have also been used. However, non-halogen flame retardant additives may be less efficient than halogenated flame retardants, thereby prompting the use of higher flame retardant additive levels to compensate for this lower efficiency. Unfortunately, the use of higher flame retardant additive levels may contribute to reduced foam physical properties.
- U.S. Pat. No. 4,746,682 to Green discloses blending alkylated triaryl phosphate esters with brominated diphenyl oxide for use as a flame retardant for polyurethane.
- U.S. Pat. No. 4,565,833 to Buszard et al. discloses the use of isopropylated phosphate esters as flame retardant agents in rigid polyurethanes or polyisocyanurates. These esters contain varying levels of triphenyl phosphate (TPP).
- TPP triphenyl phosphate
- the use of triphenyl phosphate has hereto been desirable because it was found to reduce viscosity and contribute to higher phosphorus content. Phosphorus is known to contribute to performance as a flame retardant.
- Example 2 illustrates the properties of foam samples having the minimum amount of flame retardant additive necessary to achieve a pass rating on the Cal 117 test. More particularly, Sample 1 is a comparative example in which Reofos® 35, alone, was added to the polyurethane mixture as the flame retardant. Samples 2-5 use a two component blend of an (alkyl substituted) triaryl phosphate ester/phosphorous-containing flame retardant in accordance with the present invention.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
- Fireproofing Substances (AREA)
Abstract
Flame retardant flexible polyurethane foam compositions, methods of flame retarding flexible polyurethane foam compositions, articles made therefrom and flame retardants that comprise blends of (alkyl substituted) triaryl phosphate ester and phosphorus-containing flame retardant having at least about 5 wt. % phosphorus additives. The combined weight of the (alkyl substituted) triaryl phosphate ester and the phosphorus-containing flame retardant comprises about 5 to about 40% by weight of the flexible polyurethane foam compositions or reaction mixtures. The ratio of the (alkyl substituted) triaryl phosphate ester to the phosphorus-containing flame retardant is from about 95:5 to about 50:50 percent by weight.
Description
- This application claims priority to U.S. Provisional Application No. 60/381,915, filed on May 20, 2002.
- 1. Field of the Invention
- The present invention relates to flame retardant polyurethane compositions, and more particularly to flame retardant flexible polyurethane foam compositions, methods of flame retarding flexible polyurethane foam compositions, articles made therefrom and flame retardants that comprise blends of alkylated triaryl phosphate esters and phosphorus-containing flame retardant additives.
- 2. Description of Related Art
- Polyurethanes are polymers produced by the reaction of an isocyanate and a hydroxyl-containing material, such as a polyol. Polyurethanes are available in many different forms including a flexible foam, which is typically formed by treating a polyol with a diisocyanate in the presence of water and a catalyst. This reaction results in a flexible foam composition having an abundance of carbon-hydrogen bonds, a large surface area, and an open cell structure. Due, at least in part, to these characteristics, the flexible polyurethane foam is extremely susceptible to combustion. Accordingly, flame retardant additives are often used to reduce the risk and severity of flexible polyurethane foam combustion.
- Flame retardant additives commonly used in flexible polyurethane foams typically contain halogens. Non-halogen flame retardant additives have also been used. However, non-halogen flame retardant additives may be less efficient than halogenated flame retardants, thereby prompting the use of higher flame retardant additive levels to compensate for this lower efficiency. Unfortunately, the use of higher flame retardant additive levels may contribute to reduced foam physical properties.
- Triaryl phosphate-based flame retardant agents have been used in thermoplastic compositions. However, such agents may form a liquid deposit on the injection molds, which may adversely affect the environmental stress crack resistance of the resulting thermoplastic resins.
- Historically, the first commercially available triaryl phosphates were derived from coal tar and included tricresyl phosphate, trixylyl phosphate, and mixtures of triaryl phosphates. Isopropylated and butylated synthetic triaryl phosphates were later developed as direct substitutes for coal tar derivatives and were mainly used as plasticizers for polyvinylchloride (PVC) compositions. During the development of flame retardant applications, the trend for newer additives was toward higher performance through increased phosphorus content and lower viscosity.
- Alkylated triaryl phosphate esters have been used as flame retardants for flexible polyurethane foam for many years. These esters combine good hydrolytic and thermal stability with flame retardant efficiency provided by their phosphorus content. Triaryl phosphate esters are used either alone, or more commonly, in conjunction with halogenated additives.
- U.S. Pat. No. 4,746,682 to Green discloses blending alkylated triaryl phosphate esters with brominated diphenyl oxide for use as a flame retardant for polyurethane. U.S. Pat. No. 4,565,833 to Buszard et al. discloses the use of isopropylated phosphate esters as flame retardant agents in rigid polyurethanes or polyisocyanurates. These esters contain varying levels of triphenyl phosphate (TPP). The use of triphenyl phosphate has hereto been desirable because it was found to reduce viscosity and contribute to higher phosphorus content. Phosphorus is known to contribute to performance as a flame retardant.
- Alkylated triphenyl phosphates that have been recommended and used as flame retardants have had phosphorus contents in excess of 7.7 percent. Butylated phosphates available and recommended for use as flame retardants have a phosphorus content of at least 8 percent (AKZO-Nobel Functional Chemicals Bulletin 99-94, 1999).
- U.S. Pat. No. 5,958,993 to Blundell et al. discloses the use of resorcinol bisdiphenylphosphate (RDP) to impart flame retardency to polyurethane compositions.
- According to the present invention, it has been unexpectedly discovered that blends of (alkylated) triaryl phosphates and any phosphorus source having at least 5 wt. % phosphorus demonstrate enhanced performance as compared to the individual flame retardant components.
- According to various features, characteristics and embodiments of the present invention, which will become apparent as the description thereof proceeds, the present invention provides a flame retardant polyurethane composition including an (alkyl substituted) triaryl phosphate ester; a phosphorus-containing flame retardant having at least about 5 wt. % phosphorus and comprising at least one monomeric phosphorus-containing compound, dimeric phosphorus-containing compound or mixture thereof; and a flexible polyurethane foam reaction mixture including at least one polyol and at least one isocyanate.
- The present invention further provides a flame retardant polyurethane composition including a flexible polyurethane foam reaction mixture including at least one polyol and at least one isocyanate; and a flame retardant additive comprising an (alkyl substituted) triaryl phosphate ester; and a phosphorus-containing flame retardant comprising at least one monomeric phosphorus-containing compound, dimeric phosphorus-containing compound or mixture thereof, wherein the ratio of the (alkyl substituted) triaryl phosphate ester to the phosphorus-containing flame retardant is from about 95:5 to about 50:50 percent by weight.
- The present invention further provides a flame retardant additive for use in flame retarding a flexible polyurethane foam reaction mixture, which includes at least one polyol and at least one isocyanate. The flame retardant additive includes an (alkyl substituted) triaryl phosphate ester ester; and a phosphorus-containing flame retardant having at least about 5 wt. % phosphorus and including at least one monomeric phosphorus-containing compound or dimeric phosphorus-containing compound, wherein the combined weight of the (alkyl substituted) triaryl phosphate ester and the phosphorus-containing flame retardant comprises about 5 to about 40% by weight of the polyol.
- The present invention further provides a method of making flame retarded flexible polyurethane compositions including the steps of adding to a flexible polyurethane foam reaction mixture about 5 to about 40% by weight of polyol of a flame retardant additive comprising: an (alkyl substituted) triaryl phosphate ester; and a phosphorus-containing flame retardant having at least about 5 wt. % phosphorus and including at least one monomeric phosphorus-containing compound or dimeric phosphorus-containing compound.
- The invention relates to flame retardant flexible polyurethane foam compositions and methods of flame retarding flexible polyurethane foams. The compositions comprise an otherwise flammable flexible polyurethane foam mixture and a two component flame retardant additive. The flexible polyurethane foam may be any well known, industrial polyurethane composition. Such flexible polyurethane foam mixtures generally include at least one polyol and at least one isocyanate. The two-component flame retardant additive generally includes one or more (alkyl substituted) triaryl phosphate esters (Component A), and a phosphorous-containing flame retardant additive having at least 5 wt. % phosphorus (Component B) and including at least one monomeric or dimeric phosphorous-containing compound.
- Examples of (alkyl substituted) triaryl phosphate esters suitable for use as Component A according to the present invention are represented by the general structure (I), illustrated below, where each R is independently either a linear or branched C 1 to C6 alkyl group, and n is an integer of 0, 1 or 2.
- In general, the alkylated triaryl phosphate esters used in the present invention contain from about 6 wt. % to about 9 wt. % phosphorus, depending on the degree of alkylation. Specific examples of (alkyl substituted) triaryl phosphate esters that have structure (I) and that are suitable for use as Component A include: tricresyl phosphate, butylated triphenyl phosphate, isopropylated triphenyl phosphate, and triphenyl phosphate. Examples of (alkyl substituted) triaryl phosphate esters that have been found to be particularly useful as Component A include isopropylated triphenyl phosphates. It should be understood that Component A may be a pure compound such as 4-isopropylphenyl (diphenyl phosphate). Alternatively, Component A may comprise a mixture of alkylated triaryl phosphates in which each individual ring may contain 0, 1 or 2 isopropyl groups. For instance, a mixture of (alkyl substituted) triaryl phosphate esters that has been found to produce desired results as Component A is a mixed isopropylated triphenyl phosphate containing about 8.6% phosphorus and also having about 35 wt. % of non-alkylated triphenyl phosphate. This particular (alkyl substituted) triaryl phosphate ester is sold under the tradename Reofos® 35 and is available from Great Lakes Chemical Corp.
- The phosphorous-containing flame retardant additive used as Component B can be any monomeric or dimeric-containing, non-halogen containing phosphorus source that has at least about 5 wt. % phosphorus, and that is not a triaryl phosphate ester represented by the general structure (I) above. Non-halogenated phosphorous sources having less than about 5 wt. % phosphorus may also be used, but it has been determined that excessively high amounts of such phosphorous sources may be required to provide the desired levels of flame retardancy.
- Phosphorus sources suitable for use as Component B according to the present invention include phosphates, phosphonates, phosphinates, phosphites and phosphine oxides. These phosphorous sources may contain various alkyl, aryl, or alkaryl groups provided that the size of the group does not cause the phosphorus content to be lower than about 5 wt. %. The phosphorous-containing flame retardant additive may include monomeric, dimeric and/or oligomeric phosphorous sources, but preferably include a substantial amount of monomeric and/or dimeric phosphorous sources.
- Phosphorous-containing flame retardant additives particularly suitable for use as Component B include phosphates and phosphonates having one or two phosphorus atoms per molecule. Examples include triethyl phosphate, tris(2-ethylhexyl)phosphate, dimethylmethyl phosphonate, dimethylpropyl phosphonate, and isodecyl diphenyl phosphate. Phosphorous-containing flame retardant additives that have been found to produce desired results according to the present invention include resorcinol bis(diphenyl phosphate) (RDP), tri-n-butyl phosphate (TBP) and tri-iso-butyl phosphate (TiBP).
- Components A and B are used in ratios that are readily determined to provide the best balance of properties. These ratios of Component A to Component B are generally from about 95:5 to about 50:50 wt. %, and more typically from about 95:5 to about 80:20. Ratios of about 90 wt. % of the isopropylated triphenyl phosphates to about 10 wt. % of the resorcinol bis(diphenyl phosphate), tri-n-butyl phosphate or tri-iso-butyl phosphate have been found to produce desirable results according to the present invention.
- Basically, flexible polyurethane foam compositions can be made according to the present invention by reacting an isocyanate with a polyol in the presence of a foam-forming agent and a blend of (alkyl substituted) triaryl phosphate esters and phosphorus-containing flame retardant additives. Components A and B may be pre-combined before being added to the polyurethane foam reaction mixture, such that the combined Components A and B may be provided as a single flame retardant additive package. Alternatively, Components A and B may be added individually to the polyurethane reaction mixture reactants. When used as a pre-combined package, the A and B combination is typically used in an amount of from about 5 to about 40 php (parts per hundred polyol) based on the polyol used in the polyurethane foam reaction mixture.
- The blends of the (alkyl substituted) triaryl phosphate esters and phosphorus-containing flame retardants of the present invention can be used in conjunction with other conventional additives that are used in polyurethane foam compositions such as catalysts, surfactants, cross linkers, dyes, fillers, etc. In addition, the blends of the (alkyl substituted) triaryl phosphate esters and phosphorus-containing flame retardants of the present invention can be used in other types of polymer compositions used to produce synthetic polymers such as thermoplastic polymers, including polyurethanes.
- The flame retardant flexible polyurethane foams of the present invention are useful as cushioning materials in home furnishing and automotive applications and other applications that typically involve the use of flexible foam materials.
- The features and characteristics of the present invention are further illustrated below in the following non-limiting Examples.
- In this example, flexible polyurethane foam samples were prepared, which had a density of 1.8 lbs/ft 3 (28.8 kg/m3) and incorporated either a single component flame retardant additive or the flame retardant additive of the present invention. The formulations used in producing the foam samples include the flame retardant additives listed in Table 1 together with, tolylene diisocyanate (TDI) at an index* of 110 and the following reactants:
56.6 OH Polyether Polyol 100.00 parts by weight (Hydroxy No. 56.6; Molecular Weight of 3000) Water 3.50 parts by weight Amine Catalyst (Dabco 8264)** 0.50 parts by weight Silicone Surfactant (Osi L-620)*** 1.00 parts by weight Tin Catalyst (Dabco T-9)** 0.51 parts by weight - The foam samples were prepared by mixing the polyol and the flame retardant additive together. The remaining components of the formulations, except for the isocyanate, were added and stirred into the polyol/flame retardant mixture. Finally, the isocyanate was added and stirred into the mixture. The reaction mixture was then poured into a box and allowed to expand fully. The box containing the expanded foam was placed in a ventilated 110° C. oven for 30 minutes (1,800 sec) to accelerate curing. Foam samples were removed from the boxes and stored under ambient conditions for at least twenty four hours prior to testing. All of the resulting foam samples had similar densities of about 1.8 lbs/ft 3 (28.8 kg/m3) and similar porosities of about 2 ft3/min (56.6 L/min) airflow.
- The samples were then tested using the “Cal 117” test in order to evaluate flame retardant properties. The “Cal 117” test is a vertical burn test described by the State of California Department of Consumer Affairs, Bureau of Home Furnishings, Technical Bulletin No. 117, REQUIREMENTS, TEST PROCEDURE AND APPARATUS FOR TESTING THE FLAME RETARDANCE OF RESILIENT FILLING MATERIALS USED IN UPHOLSTERED FURNITURE, January 1980, which is incorporated herein by reference.
- Table 1 illustrates the properties of foam samples having the minimum amounts of flame retardant additive necessary to achieve a pass rating in the Cal 117 test. More particularly, samples 1-6 are comparative samples in which single component flame retardant additives were used. Samples 7-14 use an (alkyl substituted) triaryl phosphate ester/phosphorous-containing flame retardant blend in accordance with the present invention. As illustrated in Table 1, the foam samples using the two component flame retardant blend of the present invention demonstrated an increase in flame retardant efficiency, requiring less flame retardant additive (as compared to the single component flame retardant additive) to achieve effective flame retardation.
TABLE 1 Sam- Quantity of Flame ple Retardant Additive Re- No. (parts per hundred polyol) sult Single Component Flame Retardant Additive 1. Reofos ® 35 12 pass 2. Reofos ® RDP 18 pass 3. Reomol ® TiBP >18 pass 4. Reomol ® TBP >18 pass 5. Reomol ® TOP >18 pass 6. Kronitex ® TCP 14 pass Two Component Flame Retardant Additive (Component A:Component B) 7. Reofos ® 35/RDP 9 pass (90:10) 8. Reofos ® 35/RDP 11 pass (80:20 ratio) 9. Reofos ® 35/RDP 18 pass (70:30 ratio) 10. Reofos ® 35/TiBP 9 pass (90:10 ratio) 11. Reofos ® 35/TBP 9 pass (90:10 ratio) 12. Reofos ® 35/Reomol ® TOP 9 pass (90:10) 13. Kronitex ® TCP/RDP (90:10) 9 pass 14. Kronitex ® TCP/TiBP 9 pass (90:10) - Flame-retarded polyurethane foam samples were prepared, which had a density of 1.2 lbs/ft 3 (19.2 kg/m3), a porosity of 6 ft3/min (169 L/min) air flow, and which incorporated either a single component flame retardant additive or the two component flame retardant additive of the present invention. The samples were prepared using the procedure described above in Example I, the flame retardant additives listed in Table 2 and the following formulation:
56.6 OH Polyether Polyol 100.00 parts by weight (Hydroxy No. 56.6; Molecular Weight of 3000) Water 6.20 parts by weight Amine Catalyst (Dabco 8264)* 0.50 parts by weight Silicone Surfactant (Osi L-620)** 1.00 parts by weight Tin Catalyst (Dabco T-9)* 0.56 parts by weight - The resulting polyurethane foam samples were tested using the Cal 117 test as described and referenced in Example I. Table 2 illustrates the properties of foam samples having the minimum amount of flame retardant additive necessary to achieve a pass rating on the Cal 117 test. More particularly, Sample 1 is a comparative example in which Reofos® 35, alone, was added to the polyurethane mixture as the flame retardant. Samples 2-5 use a two component blend of an (alkyl substituted) triaryl phosphate ester/phosphorous-containing flame retardant in accordance with the present invention. As illustrated in Table 2, the triaryl phosphate ester/phosphorous containing flame retardant blends demonstrated an increase in flame retardant efficiency, requiring less flame retardant additive (as compared to Reofos® 35, alone) to achieve flame retardation.
TABLE 2 Sample Flame Retardant Additive Quantity (parts No. (Component A:Component B) per hundred polyol) Result 1. Reofos ® 35 30 pass 2. Reofos ® 35/TiBP (90:10) 22 pass 3. Reofos ® 35/RDP (90:10) 22 pass 4. Reofos ® 35/RDP (80:20) 24 pass 5. Reofos ® 35/RDP (70/30) 28 pass - Although the present invention has been described with reference to particular means, materials and embodiments, from the foregoing description, one skilled in the art can easily ascertain the essential characteristics of the present invention and various changes and modifications can be made to adapt the various uses and characteristics without departing from the spirit and scope of the present invention as described above.
Claims (36)
1. A flame retardant polyurethane composition comprising:
an (alkyl substituted) triaryl phosphate ester;
a phosphorus-containing flame retardant having at least about 5 wt. % phosphorus and comprising at least one of a monomeric phosphorus-containing compound, a dimeric phosphorus-containing compound or a mixture thereof; and
a flexible polyurethane foam reaction mixture including at least one polyol and at least one isocyanate.
2. The flame retardant polyurethane composition of claim 1 , wherein the combined weight of the (alkyl substituted) triaryl phosphate ester and the phosphorus-containing flame retardant comprises about 5 to about 40% by weight of the polyol.
3. The flame retardant polyurethane composition of claim 1 , wherein the ratio of the (alkyl substituted) triaryl phosphate ester to the phosphorus-containing flame retardant is from about 95:5 to about 50:50 percent by weight.
4. The flame retardant polyurethane composition of claim 3 , wherein the ratio of the (alkyl substituted) triaryl phosphate ester to the phosphorus-containing flame retardant is from about 95:5 to about 80:20 percent by weight.
6. The flame retardant polyurethane composition of claim 5 , wherein the (alkyl substituted) triaryl phosphate ester comprises at least one of tricresyl phosphate, butylated triphenyl phosphate, isopropylated triphenyl phosphate, and triphenyl phosphate.
7. The flame retardant polyurethane composition of claim 6 , wherein the (alkyl substituted) triaryl phosphate ester comprises a mixed isopropylated triphenyl phosphate containing about 8.6% phosphorus and also having about 35 wt. % of non-alkylated triphenyl phosphate.
8. The flame retardant polyurethane composition of claim 1 , wherein the phosphorus-containing flame retardant comprises at least one of a phosphate, a phosphonate, a phosphinate, a phosphite and a phosphine oxide.
9. The flame retardant polyurethane composition of claim 8 , wherein the phosphorus-containing flame retardant comprises at least one of triethyl phosphate, tris(2-ethylhexyl)phosphate, dimethylmethyl phosphonate, dimethylpropyl phosphonate and isodecyl diphenyl phosphate.
10. The flame retardant polyurethane composition of claim 8 , wherein the phosphorus-containing flame retardant comprises at least one of resorcinol bis(diphenyl phosphate), tri-n-butyl phosphate and tri-iso-butyl phosphate.
11. A flame retardant polyurethane composition comprising:
a flexible polyurethane foam reaction mixture including at least one polyol and at least one isocyanate; and
a flame retardant additive comprising an (alkyl substituted) triaryl phosphate ester; and a phosphorus-containing flame retardant comprising at least one of a monomeric phosphorus-containing compound, a dimeric phosphorus-containing compound or a mixture thereof, wherein the ratio of the (alkyl substituted) triaryl phosphate ester to the phosphorus-containing flame retardant is from about 95:5 to about 80:20 percent by weight.
12. The flame retardant polyurethane composition of claim 11 wherein the phosphorus-containing flame retardant includes at least about 5 wt. % phosphorus.
13. The flame retardant polyurethane composition of claim 11 , wherein the combined weight of the (alkyl substituted) triaryl phosphate ester and the phosphorus-containing flame retardant comprises about 5 to about 40% by weight of the polyol.
15. The flame retardant polyurethane composition of claim 14 , wherein the (alkyl substituted) triaryl phosphate ester comprises at least one of tricresyl phosphate, butylated triphenyl phosphate, isopropylated triphenyl phosphate, and triphenyl phosphate.
16. The flame retardant polyurethane composition of claim 15 , wherein the (alkyl substituted) triaryl phosphate ester comprises a mixed isopropylated triphenyl phosphate containing about 8.6% phosphorus and also having about 35 wt. % of non-alkylated triphenyl phosphate.
17. The flame retardant polyurethane composition of claim 11 , wherein the phosphorus-containing flame retardant comprises at least one of a phosphate, a phosphonate, a phosphinate, a phosphite and a phosphine oxide.
18. The flame retardant polyurethane composition of claim 17 , wherein the phosphorus-containing flame retardant comprises at least one of triethyl phosphate, tris(2-ethylhexyl) phosphate, dimethylmethyl phosphonate, dimethylpropyl phosphonate and isodecyl diphenyl phosphate.
19. The flame retardant polyurethane composition of claim 17 , wherein the phosphorus-containing flame retardant comprises at least one of resorcinol bis(diphenyl phosphate), tri-n-butyl phosphate and tri-iso-butyl phosphate.
20. A flame retardant additive for use in flame retarding a flexible polyurethane foam reaction mixture including at least one polyol and at least one isocyanate, the flame retardant additive comprising:
an (alkyl substituted) triaryl phosphate ester; and
a phosphorus-containing flame retardant having at least about 5 wt. % phosphorus and including at least one monomeric phosphorus-containing compound or dimeric phosphorus-containing compound, wherein the combined weight of the (alkyl substituted) triaryl phosphate ester and the phosphorus-containing flame retardant comprises about 5 to about 40% by weight of the polyol.
21. The flame retardant additive of claim 20 , wherein the ratio of the (alkyl substituted) triaryl phosphate ester to the phosphorus-containing flame retardant is from about 95:5 to about 80:20 percent by weight.
23. The flame retardant additive of claim 22 , wherein the (alkyl substituted) triaryl phosphate ester comprises at least one of tricresyl phosphate, butylated triphenyl phosphate, isopropylated triphenyl phosphate, and triphenyl phosphate.
24. The flame retardant additive of claim 23 , wherein the (alkyl substituted) triaryl phosphate ester comprises a mixed isopropylated triphenyl phosphate containing about 8.6% phosphorus and also having about 35 wt. % of non-alkylated triphenyl phosphate.
25. The flame retardant additive of claim 20 , wherein the phosphorus-containing flame retardant comprises at least one of a phosphate, a phosphonate, a phosphinate, a phosphite and a phosphine oxide.
26. The flame retardant additive of claim 25 , wherein the phosphorus-containing flame retardant comprises at least one of triethyl phosphate, tris(2-ethylhexyl)phosphate, dimethylmethyl phosphonate, dimethylpropyl phosphonate and isodecyl diphenyl phosphate.
27. The flame retardant additive of claim 25 , wherein the phosphorus-containing flame retardant comprises at least one of resorcinol bis(diphenyl phosphate), tri-n-butyl phosphate and tri-iso-butyl phosphate.
28. A method of making flame retarded flexible polyurethane compositions comprising the step of:
adding to a flexible polyurethane foam reaction mixture about 5 to about 40% by weight of polyol of a flame retardant additive comprising: an (alkyl substituted) triaryl phosphate ester; and a phosphorus-containing flame retardant having at least about 5 wt. % phosphorus and including at least one monomeric phosphorus-containing compound or dimeric phosphorus-containing compound.
29. The method of claim 28 , further comprising the step of pre-combining the (alkyl substituted) triaryl phosphate ester and the phosphorus-containing flame retardant prior to the step of adding the flame retardant additive to the flexible polyurethane foam reaction mixture.
30. The method of claim 28 , wherein the ratio of the (alkyl substituted) triaryl phosphate ester to the phosphorus-containing flame retardant is from about 95:5 to about 80:20 percent by weight.
32. The method of claim 31 , wherein the (alkyl substituted) triaryl phosphate ester comprises at least one of tricresyl phosphate, butylated triphenyl phosphate, isopropylated triphenyl phosphate, and triphenyl phosphate.
33. The method of claim 32 , wherein the (alkyl substituted) triaryl phosphate ester comprises a mixed isopropylated triphenyl phosphate containing about 8.6% phosphorus and also having about 35 wt. % of non-alkylated triphenyl phosphate.
34. The method of claim 30 , wherein the phosphorus-containing flame retardant comprises at least one of a phosphates, a phosphonate, a phosphinate, a phosphite and a phosphine oxide.
35. The method claim 34 , wherein the phosphorus-containing flame retardant comprises at least one of triethyl phosphate, tris(2-ethylhexyl)phosphate, dimethylmethyl phosphonate, dimethylpropyl phosphonate and isodecyl diphenyl phosphate.
36. The method of claim 34 , wherein the phosphorus-containing flame retardant comprises at least one of resorcinol bis(diphenyl phosphate), tri-n-butyl phosphate and tri-iso-butyl phosphate.
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| US10/441,573 US20030216484A1 (en) | 2002-05-20 | 2003-05-20 | Blends of (alkyl substituted) triaryl phosphate esters with phosphorus-containing flame retardants for polyurethane foams |
| US11/333,398 US7390839B2 (en) | 2002-05-20 | 2006-01-17 | Blends of alkyl substituted triaryl phosphate esters with phosphorus-containing flame retardants for polyurethane foams |
Applications Claiming Priority (2)
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| US38191502P | 2002-05-20 | 2002-05-20 | |
| US10/441,573 US20030216484A1 (en) | 2002-05-20 | 2003-05-20 | Blends of (alkyl substituted) triaryl phosphate esters with phosphorus-containing flame retardants for polyurethane foams |
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Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4273881A (en) * | 1979-12-03 | 1981-06-16 | Basf Wyandotte Corporation | Organo-phosphorus flame-retardant for polyurethane foams prepared from graft polyoxyalkylene polyether polyols |
| US4565833A (en) * | 1982-10-12 | 1986-01-21 | Ciba-Geigy Ag | Fire retardant composition |
| US4649163A (en) * | 1984-12-07 | 1987-03-10 | Takeda Chemical Industries, Ltd. | Flame-retardant polyurethane foam and polyol composition therefor |
| US4696952A (en) * | 1984-07-26 | 1987-09-29 | Ikeda Bussan Co., Ltd. | Production of polyurethane foam |
| US4746682A (en) * | 1987-04-01 | 1988-05-24 | Fmc Corporation | Polyurethane flame retardant |
| US4910241A (en) * | 1983-08-25 | 1990-03-20 | General Electric Company | Crosslinkable flame retardant compositions of olefinic rubber and polyphenylene ether |
| US5164417A (en) * | 1990-06-01 | 1992-11-17 | Albright & Wilson Americas Inc. | Phosphate ester flame retardant mixture and foamed resins containing same |
| US5578651A (en) * | 1992-08-04 | 1996-11-26 | Bayer Aktiengesellschaft | Process for producing rigid polyurethane foams |
| US5672645A (en) * | 1993-08-26 | 1997-09-30 | Bayer Ag | Flame resistant polycarbonate/ABS moulding compounds resistant to stress cracking |
| US5728746A (en) * | 1995-11-03 | 1998-03-17 | Hoechst Aktiengesellschaft | Process for the preparation of mixtures of oligomeric phosphoric acid esters and their use as flame-proofing agents for polyurethane foams |
| US5958993A (en) * | 1994-08-30 | 1999-09-28 | Akzo Novel Nv | Fog reduction in polyurethane foam using phosphate esters |
| US6054499A (en) * | 1993-02-10 | 2000-04-25 | Rathor Ag | Prepolymer composition for insulating foams |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4206067A (en) * | 1978-10-02 | 1980-06-03 | Chevron Research Company | Thermally stabilized erosion-inhibited functional fluids containing perhalometal compounds and an organic base |
| CA2029460C (en) * | 1989-11-14 | 2004-01-06 | Gerald Fesman | Viscosity reduction of high viscosity fluid flame retardants for polyurethanes |
| US6083428A (en) * | 1995-03-07 | 2000-07-04 | Asahi Kasei Kogyo Kabushiki Kaisha | Flame-retardant resin composition |
| US5817606A (en) * | 1996-08-08 | 1998-10-06 | Rohm And Haas Company | Viscosity index improving additives for phosphate ester-containing hydraulic fluids |
| JPH10147708A (en) * | 1996-11-18 | 1998-06-02 | Meisei Kagaku Kogyo Kk | Method for producing lightweight polyurethane elastic body |
| WO2000027955A1 (en) * | 1998-11-10 | 2000-05-18 | Exxonmobil Research And Engineering Company | PHOSPHATE ESTER BASE STOCKS COMPRISING MIXED n-BUTYL/ISOBUTYL PHOSPHATE ESTERS AND AIRCRAFT HYDRAULIC FLUIDS COMPRISING THE SAME |
| US7288577B1 (en) * | 1999-09-09 | 2007-10-30 | Supresta U.S. Llc | Polyurethane foam containing flame retardant blend of non-oligomeric and oligomeric flame retardants |
| AU2002212954A1 (en) * | 2000-08-04 | 2002-02-18 | Exxonmobil Research And Engineering Company | Method for lubricating high pressure hydraulic system using phosphate ester hydraulic fluid |
| US6667355B2 (en) * | 2001-08-30 | 2003-12-23 | Pabu Services, Inc. | Higher alkylated triaryl phosphate ester flame retardants |
-
2003
- 2003-05-20 DE DE60316431T patent/DE60316431T2/en not_active Expired - Lifetime
- 2003-05-20 BR BRPI0310058-8A patent/BR0310058B8/en not_active IP Right Cessation
- 2003-05-20 JP JP2004508167A patent/JP3987068B2/en not_active Expired - Lifetime
- 2003-05-20 US US10/441,573 patent/US20030216484A1/en not_active Abandoned
- 2003-05-20 EP EP03755378A patent/EP1506256B1/en not_active Expired - Lifetime
- 2003-05-20 RU RU2004137127/04A patent/RU2004137127A/en not_active Application Discontinuation
- 2003-05-20 CN CNB038114402A patent/CN100506897C/en not_active Expired - Lifetime
- 2003-05-20 AT AT03755378T patent/ATE373691T1/en not_active IP Right Cessation
- 2003-05-20 AU AU2003273184A patent/AU2003273184A1/en not_active Abandoned
- 2003-05-20 KR KR1020047018192A patent/KR100901789B1/en not_active Expired - Fee Related
- 2003-05-20 WO PCT/US2003/015687 patent/WO2003099919A1/en not_active Ceased
-
2006
- 2006-01-17 US US11/333,398 patent/US7390839B2/en not_active Expired - Lifetime
Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4273881A (en) * | 1979-12-03 | 1981-06-16 | Basf Wyandotte Corporation | Organo-phosphorus flame-retardant for polyurethane foams prepared from graft polyoxyalkylene polyether polyols |
| US4565833A (en) * | 1982-10-12 | 1986-01-21 | Ciba-Geigy Ag | Fire retardant composition |
| US4910241A (en) * | 1983-08-25 | 1990-03-20 | General Electric Company | Crosslinkable flame retardant compositions of olefinic rubber and polyphenylene ether |
| US4696952A (en) * | 1984-07-26 | 1987-09-29 | Ikeda Bussan Co., Ltd. | Production of polyurethane foam |
| US4649163A (en) * | 1984-12-07 | 1987-03-10 | Takeda Chemical Industries, Ltd. | Flame-retardant polyurethane foam and polyol composition therefor |
| US4746682A (en) * | 1987-04-01 | 1988-05-24 | Fmc Corporation | Polyurethane flame retardant |
| US5164417A (en) * | 1990-06-01 | 1992-11-17 | Albright & Wilson Americas Inc. | Phosphate ester flame retardant mixture and foamed resins containing same |
| US5578651A (en) * | 1992-08-04 | 1996-11-26 | Bayer Aktiengesellschaft | Process for producing rigid polyurethane foams |
| US6054499A (en) * | 1993-02-10 | 2000-04-25 | Rathor Ag | Prepolymer composition for insulating foams |
| US5672645A (en) * | 1993-08-26 | 1997-09-30 | Bayer Ag | Flame resistant polycarbonate/ABS moulding compounds resistant to stress cracking |
| US5958993A (en) * | 1994-08-30 | 1999-09-28 | Akzo Novel Nv | Fog reduction in polyurethane foam using phosphate esters |
| US5728746A (en) * | 1995-11-03 | 1998-03-17 | Hoechst Aktiengesellschaft | Process for the preparation of mixtures of oligomeric phosphoric acid esters and their use as flame-proofing agents for polyurethane foams |
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Also Published As
| Publication number | Publication date |
|---|---|
| KR100901789B1 (en) | 2009-06-11 |
| EP1506256B1 (en) | 2007-09-19 |
| JP3987068B2 (en) | 2007-10-03 |
| US20060116432A1 (en) | 2006-06-01 |
| EP1506256A1 (en) | 2005-02-16 |
| BR0310058A (en) | 2005-02-15 |
| DE60316431T2 (en) | 2008-06-12 |
| KR20050012241A (en) | 2005-01-31 |
| CN100506897C (en) | 2009-07-01 |
| DE60316431D1 (en) | 2007-10-31 |
| US7390839B2 (en) | 2008-06-24 |
| CN1656165A (en) | 2005-08-17 |
| BR0310058B8 (en) | 2013-02-19 |
| WO2003099919A1 (en) | 2003-12-04 |
| JP2005526892A (en) | 2005-09-08 |
| ATE373691T1 (en) | 2007-10-15 |
| BR0310058B1 (en) | 2013-01-08 |
| AU2003273184A1 (en) | 2003-12-12 |
| RU2004137127A (en) | 2005-07-10 |
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