WO2002079315A1 - Blend of organophosphorus flame retardant, lactone stabilizer, and phosphate compatibilizer - Google Patents
Blend of organophosphorus flame retardant, lactone stabilizer, and phosphate compatibilizer Download PDFInfo
- Publication number
- WO2002079315A1 WO2002079315A1 PCT/US2001/051604 US0151604W WO02079315A1 WO 2002079315 A1 WO2002079315 A1 WO 2002079315A1 US 0151604 W US0151604 W US 0151604W WO 02079315 A1 WO02079315 A1 WO 02079315A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkyl
- flame retardant
- composition
- phosphate ester
- hydrogen
- Prior art date
Links
- 0 *c(cc1C2c3c(*)c(*)c(*)c(*)c3*)cc(*)c1OC2=O Chemical compound *c(cc1C2c3c(*)c(*)c(*)c(*)c3*)cc(*)c1OC2=O 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
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1535—Five-membered rings
- C08K5/1539—Cyclic anhydrides
-
- 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
-
- 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
- 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
- C08G18/4833—Polyethers containing oxyethylene units
- C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1535—Five-membered rings
-
- 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
- C08G2110/0083—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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S521/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S521/906—Polyurethane cellular product containing unreacted flame-retardant material
Definitions
- the present invention relates to the combination of three components in a flame retardant additive formulation that, when incorporated in a polyurethane foam, results in a considerable reduction in the discoloration (also referred to as "scorch") of that polyurethane foam as to compared to when only the two organophosphorus components of the combination are employed.
- the present invention relates to the use of a solubilizing monomeric phosphate ester component with a combination of an organophosphorus flame retardant, which in certain embodiments can be an oligomeric phosphate ester, and a benzofuran-2-one (or "lactone”) stabilizer.
- solubilizing component retards the normal solution instability that would be observed, over time, if just the organophosphorus flame retardant and benzofuran-2-one stabilizer were used together.
- organophosphorus flame retardant and benzofuran-2-one stabilizer were used together.
- Other advantages of the solubilizing component for example, PHOSFLEX® TBEP brand from Akzo Nobel Functional
- Chemicals are that the viscosity is reduced when an oligomeric organophosphorus flame retardant is used and, unlike other flammable compatibilizers , the flame retardant performance is not influenced to an appreciable degree.
- the more solution-stable composition of the present invention allows for a reduction of scorch, which normally occurs, for example, when a phosphate ester flame retardant is used, in low-density polyurethane flexible foams .
- An essential component in the flame retardant blend of the present invention is an organophosphorus flame retardant which is present in a predominant amount compared to the other two components of the three part flame retardant blend of this invention.
- the amount of the organophosphrus additive in the blend will range from about 60% to about 98%, by weight of the blend, more preferably from about 80% to about 96%.
- Representative examples of such flame retardants include tris (dichloroisopropyl) phosphate, tris (2-chloroisopropyl) phosphate, and tris (2-chloroethyl) phosphate.
- the organophosphorus flame retardant component can be an oligomeric organophosphorus flame retardant, preferably having a phosphorus content of no less than about 5%, by weight and, in preferred embodiments when an organophosphate is desired, at least three phosphate ester units therein (i.e., at least two phosphate ester repeat units and a phosphate capping unit) .
- oligomeric as used herein is meant to exclude either monomeric or dimeric species .
- a representative organophosphorus additive of this type is generally described in U.S. Patent No. 4,382,042 to T.A. Hardy with the non-halogenated versions being preferred (e.g., especially the ethyl group-containing composition) .
- organophosphate oligomers can be formed by reacting phosphorus pen oxide with the selected trialkyl phosphate (e.g., triethyl phosphate) to form a polyphosphate ester containing P-O-P bonds that is then reacted with epoxide (e.g., ethylene oxide) to form the desired product.
- epoxide e.g., ethylene oxide
- n (which designates the "repeat” phosphate ester units) can range, on a number average basis, from 2 to about 20, preferably from 2 to about 10
- R is selected from the group consisting of alkyl and hydroxyalkyl and R' is alkylene.
- the alkyl and alkylene groups will generally contain from about two to about ten carbon atoms .
- oligomeric phosphates for use herein will comprise ethyl and ethylene groups as the alkyl and alkylene moieties, will have a hydroxy functionality of no more than about 30 mg KOH/g, will have an acid number of no more than about 2.5 mg KOH/g, and will have a phosphorus content that ranges from about 15% to about 25%, by weight. It is referred to herein after as "PEEOP" (or “poly (ethyl ethyleneoxy) hosphate”) .
- oligomeric phosphonate-containing materials as component (b) .
- oligomeric phosphonate-containing materials are intended to be included. These have the same structure as depicted above for the oligomeric phosphate species with the exception that the internal (bracketed) RO- on the left side of the structure may be R- and one of the terminal -OR structures on the right side of the formula may be —R.
- a representative and commercially available example of an additive of this type is FYROL 51 from Akzo Nobel Chemicals Inc. which is made by a multistep process from dimethyl methylphosphonate, phosphorus pentoxide, ethylene glycol, and ethylene oxide.
- FYROL ® PNX is a preferred product of this type for use herein. It is an oligomeric phosphate ester (CAS # 184538-58-7) of the formula:
- n (which designates the "repeat” phosphate ester units) is, on a number average basis, of from about 2 to about 20, R is ethyl, and R' is ethylene. This preferred has a phosphorus content of about 19 wt% and a viscosity at 25°C of about 2000 mPa. s .
- the second essential component of the flame retardant blend of the present invention is of the type of benzofuran-2-one stabilizer that is described in U.S. Patent No. 5,869,565, which is incorporated herein by reference for its illustration of such an additive.
- the structure of this class of stabilizer is provided in the following formulae:
- R_ f R 7 , Re, R 9 and Rio are each independently of the other C 1 -C 4 alkyl or C 1 -C 4 alkoxy, the others being hydrogen, or R 7 to Rio are hydrogen, or at most two of these radicals are each independently of the other methyl or methoxy
- Ri is -O-CHR 3 -CHR 5 -O-CO—R 6
- R 2 and R 4 are each independently of the other hydrogen or C ⁇ _C 6 alkyl
- R 3 is hydrogen or C 1 -C 4 alkyl
- R 5 is hydrogen, phenyl or C ⁇ -C 6 alkyl
- R 6 is C 1 -C 4 alkyl.
- HP-136 brand product from Ciba Specialty Chemicals is a preferred species for use herein and is (5,7-di-t-butyl-3 (3,4 dimethylphenyl) -3H-benzofuran-2-one, wherein R 2 and R 4 are each t-butyl and two of Ri , R7 , Re, R9 and Rio are each methyl .
- This stabilizer component is present in the flame retardant blend of the present invention at from about 0.05% to about 1.0%, by weight of the blend, more preferably from about 0.2% to about 0.5%.
- R is independently selected from alkyl , alkoxyalkyl , or haloalkyl containing up to about 8 carbon atoms in the alkyl , alkoxyalkyl and/or haloalkyl groups. It is present at from about 1% to about 40%, by weight of the blend, more preferably from about
- Representative compounds of this type that can be selected include tributoxyethyl phosphate, tri (1,3 dichloroisopropyl) phosphate, tributyl phosphate, tri (2-chloroethyl)phosphate, triethylphosphate, tri (2-chloroisopropyl)phosphate, isopropylated triarylphosphate, and a tert-butylated triphenyl phosphate mixture.
- a monomeric phosphate compatibilizers from the same general type of organophosphorus compound that could be selected for the predominant component of this invention (which will normally be a compound that does not form a compatible blend with the benzo-2-furanone stabilizer
- the present invention contemplates that a differing compound from within that class will be selected so that there are three components in the flame retardant blend.
- the previously described flame retardant blend can be incorporated in conventional polyurethane foams at use levels of up to about 24 parts by weight per one hundred parts of polyol (which will normally contain antioxidants for scorch inhiubition) to confer the desired degree of flame retardancy and antiscorch behavior on those foams .
- System 1 which is described below, uses FYROL ® 38 as a solubilizer for the lactone additive HP-136 with FYROL ® PNX.
- System 2 uses a phosphate ester, PHOSFLEX ® TBEP as a solubilizer for HP-136 with the FYROL ® PNX material.
- a microwave oven test method was used as a means to determine the degree of discoloration in the tested foams with a numerical scale of 1 to 5 being used to assign the degree of scorch present in the foam.
- a value of 1 was assigned to a white foam control showing no discoloration, whereas the value of 5 was assigned to a very dark brown scorch pattern. The values increased from 1 to 5 with increasing discoloration.
- Foams prepared with either system (flame retardant, solubilizer, and lactone additive) produced foams with a 1.5 to 2.0 rating, whereas without the use of the HP-136 lactone stabilizer the level of scorch was rated at 2.5 to 3.0.
- the nominal density was 1.20 pcf (pounds per cubic foot) .
- Fyrol ® PNX mixed with only HP-136 was difficult to dissolve and did not form a clear, stable solution; therefore, a compatibilizer or solubilizer, in accordance with the present invention, was necessary to maintain a stable solution.
- the formulation components mentioned in Table A, above, were combined and poured into a (8.0" x 8.0" x 5.0") box and allowed to rise freely. The foam was then placed in a GE PROFILE SENSOR microwave oven and heated for one hundred and twenty seconds. The foam was removed from the oven. It was cooled to room temperature for two hours . The foam bun was cut into a 1 inch slice in a perpendicular to rise direction and was examined for its discoloration rating.
- a second set of foams was produced using system 2 but the scorch characteristics of the foams were measured using a colorimeter (namely, the DR LANGE Micro Color apparatus) .
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE60133482T DE60133482T2 (en) | 2000-11-13 | 2001-11-13 | MIXTURE OF ORGANOPHOSPHOR FLAME PROTECTION AGENT, LACTON STABILIZER, AND PHOSPHATE COMPATIBILIZATION AGENT |
EP01273813A EP1334149B1 (en) | 2000-11-13 | 2001-11-13 | Blend of organophosphorus flame retardant, lactone stabilizer, and phosphate compatibilizer |
JP2002578327A JP2004519547A (en) | 2000-11-13 | 2001-11-13 | Mixture of organophosphorus flame retardant, lactone stabilizer and phosphate compatibilizer |
CA002428540A CA2428540A1 (en) | 2000-11-13 | 2001-11-13 | Blend of organophosphorus flame retardant, lactone stabilizer, and phosphate compatibilizer |
US10/433,968 US7122135B2 (en) | 2000-11-13 | 2001-11-13 | Blend of organophosphorus flame retardant, lactone stabilizer, and phosphate compatibilizer |
KR10-2003-7006418A KR20030063377A (en) | 2000-11-13 | 2001-11-13 | Blend of organophosphorus flame retardant, lactone stabilizer, and phosphate compatibilizer |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24754100P | 2000-11-13 | 2000-11-13 | |
US60/247,541 | 2000-11-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2002079315A1 true WO2002079315A1 (en) | 2002-10-10 |
Family
ID=22935283
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2001/051604 WO2002079315A1 (en) | 2000-11-13 | 2001-11-13 | Blend of organophosphorus flame retardant, lactone stabilizer, and phosphate compatibilizer |
Country Status (9)
Country | Link |
---|---|
US (1) | US7122135B2 (en) |
EP (1) | EP1334149B1 (en) |
JP (1) | JP2004519547A (en) |
KR (1) | KR20030063377A (en) |
CN (1) | CN1240760C (en) |
AT (1) | ATE391149T1 (en) |
CA (1) | CA2428540A1 (en) |
DE (1) | DE60133482T2 (en) |
WO (1) | WO2002079315A1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005105911A1 (en) * | 2004-04-27 | 2005-11-10 | Supresta Llc | Low scorching flame retardants for polyurethane foams |
WO2005118699A1 (en) * | 2004-04-27 | 2005-12-15 | Supresta Llc | Low scorching flame retardants for colored polyurethane foams |
US20130172435A1 (en) * | 2012-01-03 | 2013-07-04 | Iran OTERO MARTINEZ | Flame-retardant polyurethane foams |
EP2612876A1 (en) | 2012-01-03 | 2013-07-10 | Basf Se | Flame-proof polyurethane foams |
EP2687535A1 (en) | 2012-07-20 | 2014-01-22 | LANXESS Deutschland GmbH | Halogen-free poly(alkylene phosphate) |
EP3660064A1 (en) | 2018-11-28 | 2020-06-03 | LANXESS Deutschland GmbH | Compositions with enhanced efficacy as flame retardants |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7833441B2 (en) * | 2003-05-09 | 2010-11-16 | Prometheus Developments Limited | Method of producing a polymeric material |
US20110046250A1 (en) * | 2007-07-06 | 2011-02-24 | Stowell Jeffrey K | Flame retardant composition and flexible polyurethane foam prepared therewith |
EP2816066A1 (en) * | 2013-06-19 | 2014-12-24 | Basf Se | Low emission, stabilised polyurethane |
EP2848640A1 (en) * | 2013-09-13 | 2015-03-18 | LANXESS Deutschland GmbH | Phosphoric acid ester compositions with reduced hygroscopicity |
JP5782148B2 (en) * | 2014-03-14 | 2015-09-24 | ダウ グローバル テクノロジーズ エルエルシー | Halogen-free flame retardant TPU composite |
CN115895036A (en) * | 2022-11-28 | 2023-04-04 | 云南云天化股份有限公司 | Flame retardant composition, polyurethane foam and preparation method thereof |
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US5308899A (en) * | 1991-11-19 | 1994-05-03 | Ciba-Geigy Corporation | Polyether polyol and polyurethane compositions protected against oxidation and core scorching |
US5367008A (en) * | 1992-05-22 | 1994-11-22 | Ciba-Geigy Corporation | 3-(alkoxyphenyl)benzofuran-2-ones as stabilisers |
US5369159A (en) * | 1992-05-22 | 1994-11-29 | Ciba-Geigy Corporation | 3-(acyloxyphenyl)benzofuran-2-one stabilizers |
EP0867467A1 (en) * | 1997-03-26 | 1998-09-30 | General Electric Company | Compositions stabilized with tertiary amine oxides |
US5844026A (en) * | 1997-06-30 | 1998-12-01 | Ciba Specialty Chemicals Corporation | N,N',N''-tris{2,4-bis Hydrocarbyloxy-2,2,6,6-tetra-methylpiperidin-4-yl)alkylamino!-s-triazin-6-yl}-3,3'-ethylenediiminodipropylamines, their isomers and bridged derivatives and polymer compositions stabilized therewith |
WO1999003915A1 (en) * | 1997-07-14 | 1999-01-28 | Dover Chemical Corporation | Lactone/phosphite blends |
WO1999067223A2 (en) * | 1998-06-22 | 1999-12-29 | Cytec Tech Corp | Trisaryl-1,3,5-triazine ultraviolet light absorbers containing hindered phenols |
JP2000154289A (en) * | 1998-11-20 | 2000-06-06 | Asahi Chem Ind Co Ltd | Flame-retardant resin composition |
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2001
- 2001-11-13 CA CA002428540A patent/CA2428540A1/en not_active Abandoned
- 2001-11-13 AT AT01273813T patent/ATE391149T1/en not_active IP Right Cessation
- 2001-11-13 CN CNB018188273A patent/CN1240760C/en not_active Expired - Fee Related
- 2001-11-13 JP JP2002578327A patent/JP2004519547A/en active Pending
- 2001-11-13 EP EP01273813A patent/EP1334149B1/en not_active Expired - Lifetime
- 2001-11-13 WO PCT/US2001/051604 patent/WO2002079315A1/en active Application Filing
- 2001-11-13 DE DE60133482T patent/DE60133482T2/en not_active Expired - Lifetime
- 2001-11-13 US US10/433,968 patent/US7122135B2/en not_active Expired - Fee Related
- 2001-11-13 KR KR10-2003-7006418A patent/KR20030063377A/en not_active Application Discontinuation
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005105911A1 (en) * | 2004-04-27 | 2005-11-10 | Supresta Llc | Low scorching flame retardants for polyurethane foams |
WO2005118699A1 (en) * | 2004-04-27 | 2005-12-15 | Supresta Llc | Low scorching flame retardants for colored polyurethane foams |
JP2007534831A (en) * | 2004-04-27 | 2007-11-29 | スプレスタ エルエルシー | Low scorch flame retardant for polyurethane foam |
US20130172435A1 (en) * | 2012-01-03 | 2013-07-04 | Iran OTERO MARTINEZ | Flame-retardant polyurethane foams |
EP2612876A1 (en) | 2012-01-03 | 2013-07-10 | Basf Se | Flame-proof polyurethane foams |
WO2013102535A1 (en) | 2012-01-03 | 2013-07-11 | Basf Se | Flame-protected polyurethane foams |
US10640602B2 (en) | 2012-01-03 | 2020-05-05 | Basf Se | Flame-retardant polyurethane foams |
EP2687535A1 (en) | 2012-07-20 | 2014-01-22 | LANXESS Deutschland GmbH | Halogen-free poly(alkylene phosphate) |
EP2687534A1 (en) | 2012-07-20 | 2014-01-22 | LANXESS Deutschland GmbH | Halogen-free poly(alkylene phosphate) |
EP3660064A1 (en) | 2018-11-28 | 2020-06-03 | LANXESS Deutschland GmbH | Compositions with enhanced efficacy as flame retardants |
EP3660065A1 (en) | 2018-11-28 | 2020-06-03 | LANXESS Deutschland GmbH | Compositions with enhanced efficacy as flame retardants |
Also Published As
Publication number | Publication date |
---|---|
CA2428540A1 (en) | 2002-10-10 |
ATE391149T1 (en) | 2008-04-15 |
DE60133482D1 (en) | 2008-05-15 |
KR20030063377A (en) | 2003-07-28 |
CN1474852A (en) | 2004-02-11 |
EP1334149A1 (en) | 2003-08-13 |
JP2004519547A (en) | 2004-07-02 |
US20050107500A1 (en) | 2005-05-19 |
DE60133482T2 (en) | 2009-05-20 |
US7122135B2 (en) | 2006-10-17 |
CN1240760C (en) | 2006-02-08 |
EP1334149B1 (en) | 2008-04-02 |
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