GB919067A - Phosphorus containing polyurethane foams - Google Patents
Phosphorus containing polyurethane foamsInfo
- Publication number
- GB919067A GB919067A GB2489761A GB2489761A GB919067A GB 919067 A GB919067 A GB 919067A GB 2489761 A GB2489761 A GB 2489761A GB 2489761 A GB2489761 A GB 2489761A GB 919067 A GB919067 A GB 919067A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- acids
- polyester
- phosphorus
- phosphorous
- 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.)
- Expired
Links
- 239000011574 phosphorus Substances 0.000 title abstract 10
- 229910052698 phosphorus Inorganic materials 0.000 title abstract 10
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title abstract 6
- 229920005830 Polyurethane Foam Polymers 0.000 title 1
- 239000011496 polyurethane foam Substances 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 16
- 229920000728 polyester Polymers 0.000 abstract 14
- -1 ethylene, propylene, butylene Chemical group 0.000 abstract 8
- 150000007513 acids Chemical class 0.000 abstract 7
- 239000007795 chemical reaction product Substances 0.000 abstract 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 7
- 239000000203 mixture Substances 0.000 abstract 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract 6
- 229920000570 polyether Polymers 0.000 abstract 6
- 229920000642 polymer Polymers 0.000 abstract 6
- 238000000034 method Methods 0.000 abstract 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 4
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 abstract 4
- 235000011037 adipic acid Nutrition 0.000 abstract 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 abstract 4
- DJKGDNKYTKCJKD-UHFFFAOYSA-N chlorendic acid Chemical compound ClC1=C(Cl)C2(Cl)C(C(=O)O)C(C(O)=O)C1(Cl)C2(Cl)Cl DJKGDNKYTKCJKD-UHFFFAOYSA-N 0.000 abstract 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 4
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 abstract 4
- 229920001228 polyisocyanate Polymers 0.000 abstract 4
- 239000005056 polyisocyanate Substances 0.000 abstract 4
- 150000005846 sugar alcohols Polymers 0.000 abstract 4
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 abstract 4
- JYFHYPJRHGVZDY-UHFFFAOYSA-N Dibutyl phosphate Chemical class CCCCOP(O)(=O)OCCCC JYFHYPJRHGVZDY-UHFFFAOYSA-N 0.000 abstract 3
- 239000001361 adipic acid Substances 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 abstract 3
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 abstract 3
- 229940029284 trichlorofluoromethane Drugs 0.000 abstract 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 2
- 239000004254 Ammonium phosphate Substances 0.000 abstract 2
- 238000005698 Diels-Alder reaction Methods 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- 229910019142 PO4 Inorganic materials 0.000 abstract 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 abstract 2
- 239000000654 additive Substances 0.000 abstract 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 2
- 229910000148 ammonium phosphate Inorganic materials 0.000 abstract 2
- 235000019289 ammonium phosphates Nutrition 0.000 abstract 2
- 150000008064 anhydrides Chemical class 0.000 abstract 2
- 239000010425 asbestos Substances 0.000 abstract 2
- 235000011132 calcium sulphate Nutrition 0.000 abstract 2
- 239000001175 calcium sulphate Substances 0.000 abstract 2
- 235000013877 carbamide Nutrition 0.000 abstract 2
- 230000001413 cellular effect Effects 0.000 abstract 2
- 239000004927 clay Substances 0.000 abstract 2
- 229910052570 clay Inorganic materials 0.000 abstract 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 abstract 2
- 125000005442 diisocyanate group Chemical group 0.000 abstract 2
- GOJNABIZVJCYFL-UHFFFAOYSA-N dimethylphosphinic acid Chemical compound CP(C)(O)=O GOJNABIZVJCYFL-UHFFFAOYSA-N 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- 150000002118 epoxides Chemical class 0.000 abstract 2
- 239000000945 filler Substances 0.000 abstract 2
- 230000009970 fire resistant effect Effects 0.000 abstract 2
- 239000006260 foam Substances 0.000 abstract 2
- 239000004088 foaming agent Substances 0.000 abstract 2
- 235000019253 formic acid Nutrition 0.000 abstract 2
- 239000003365 glass fiber Substances 0.000 abstract 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 abstract 2
- QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 230000004048 modification Effects 0.000 abstract 2
- 238000012986 modification Methods 0.000 abstract 2
- 150000002989 phenols Chemical class 0.000 abstract 2
- 235000021317 phosphate Nutrition 0.000 abstract 2
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 abstract 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical group [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 abstract 2
- 150000003013 phosphoric acid derivatives Chemical group 0.000 abstract 2
- 239000000376 reactant Substances 0.000 abstract 2
- 229910052895 riebeckite Inorganic materials 0.000 abstract 2
- 150000003333 secondary alcohols Chemical class 0.000 abstract 2
- 229920002994 synthetic fiber Polymers 0.000 abstract 2
- 150000003509 tertiary alcohols Chemical class 0.000 abstract 2
- 150000003672 ureas Chemical class 0.000 abstract 2
- NOJBUSGDSMAHQU-UHFFFAOYSA-N (4-octadecoxyphenyl)-(2-phenyloxiran-2-yl)methanone Chemical compound C1(=CC=CC=C1)C1(CO1)C(C1=CC=C(C=C1)OCCCCCCCCCCCCCCCCCC)=O NOJBUSGDSMAHQU-UHFFFAOYSA-N 0.000 abstract 1
- WSWCOQWTEOXDQX-MQQKCMAXSA-M (E,E)-sorbate Chemical compound C\C=C\C=C\C([O-])=O WSWCOQWTEOXDQX-MQQKCMAXSA-M 0.000 abstract 1
- WMMGRPSGJRRNLN-UHFFFAOYSA-N 1-$l^{1}-phosphanylbutane Chemical compound CCCC[P] WMMGRPSGJRRNLN-UHFFFAOYSA-N 0.000 abstract 1
- GELKGHVAFRCJNA-UHFFFAOYSA-N 2,2-Dimethyloxirane Chemical class CC1(C)CO1 GELKGHVAFRCJNA-UHFFFAOYSA-N 0.000 abstract 1
- PJOUFZLECMLIAX-UHFFFAOYSA-N 2-(butylsulfanylmethyl)oxirane Chemical compound CCCCSCC1CO1 PJOUFZLECMLIAX-UHFFFAOYSA-N 0.000 abstract 1
- LKMJVFRMDSNFRT-UHFFFAOYSA-N 2-(methoxymethyl)oxirane Chemical compound COCC1CO1 LKMJVFRMDSNFRT-UHFFFAOYSA-N 0.000 abstract 1
- BVXKWTBRQORZNE-UHFFFAOYSA-N 2-(methylsulfonylmethyl)oxirane Chemical compound CS(=O)(=O)CC1CO1 BVXKWTBRQORZNE-UHFFFAOYSA-N 0.000 abstract 1
- SNZYOYGFWBZAQY-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;2-methyloxirane Chemical compound CC1CO1.CCC(CO)(CO)CO SNZYOYGFWBZAQY-UHFFFAOYSA-N 0.000 abstract 1
- GQICKXRCZNGDLY-UHFFFAOYSA-N 2-ethyl-3-methyl-2-pentyloxirane Chemical compound C(C)C1(C(C)O1)CCCCC GQICKXRCZNGDLY-UHFFFAOYSA-N 0.000 abstract 1
- LIESJAYIOKBLIL-UHFFFAOYSA-N 2-methyl-3-propyloxirane Chemical compound CCCC1OC1C LIESJAYIOKBLIL-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract 1
- BBGQARREKZWTAT-UHFFFAOYSA-N C(CCC)P(O)(O)O Chemical compound C(CCC)P(O)(O)O BBGQARREKZWTAT-UHFFFAOYSA-N 0.000 abstract 1
- GFMYEVPBEJFZHH-UHFFFAOYSA-N CP(O)(O)O Chemical compound CP(O)(O)O GFMYEVPBEJFZHH-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 abstract 1
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 abstract 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- 150000001279 adipic acids Chemical class 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 1
- BNMJSBUIDQYHIN-UHFFFAOYSA-N butyl dihydrogen phosphate Chemical class CCCCOP(O)(O)=O BNMJSBUIDQYHIN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000002311 glutaric acids Chemical class 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000002440 hydroxy compounds Chemical class 0.000 abstract 1
- 150000002691 malonic acids Chemical class 0.000 abstract 1
- PMVVRSKJCGEFIY-UHFFFAOYSA-N methylphosphonous acid Chemical compound CP(O)O PMVVRSKJCGEFIY-UHFFFAOYSA-N 0.000 abstract 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 abstract 1
- 150000002913 oxalic acids Chemical class 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 abstract 1
- 150000003017 phosphorus Chemical class 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 229940075554 sorbate Drugs 0.000 abstract 1
- 150000003444 succinic acids Chemical class 0.000 abstract 1
- 125000000565 sulfonamide group Chemical group 0.000 abstract 1
- 125000001174 sulfone group Chemical group 0.000 abstract 1
- AKXUUJCMWZFYMV-UHFFFAOYSA-M tetrakis(hydroxymethyl)phosphanium;chloride Chemical compound [Cl-].OC[P+](CO)(CO)CO AKXUUJCMWZFYMV-UHFFFAOYSA-M 0.000 abstract 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical class CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 abstract 1
- 150000004072 triols Chemical class 0.000 abstract 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3878—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Epoxy Resins (AREA)
Abstract
A process for the production of a fire resistant cellular reaction product comprises reacting (1) a hydroxyl-containing polymer having a hydroxyl number of between about 25 and 900, (2) an organic polyisocyanate, and (3) from 5 to 30% by weight, based on the weight of the hydroxyl-containing polymer of a phosphorus acid or a partially esterified phosphorus acid or mixtures thereof. The hydroxyl-containing polymer may be a polyester, polyether or mixtures thereof. As a modification an organic diisocyanate is first reacted with a polyester to form a prepolymer and this prepolymer is then reacted with a polyether and/or further polyester and with the phosphorus acid or partially esterified phosphorus acid. The polyesters may be prepared from malaeic, fumaric, phthalic, tetrachlorophthalic, oxalic, malonic, succinic, glutaric or adipic acids, or Diels-Alder adducts of hexahalocyclopentadiene and a polycarboxylic compound. As hydroxy compounds there may be used glycols, triols, pentaerythritol or a Diels-Alder adduct of a hexahalocyclopentadiene and a polyhydric alcohol. The polyethers are reaction products of a polyhydric alcohol or polycarboxylic acid with an epoxide such as ethylene, propylene, butylene or isobutylene oxides, 2,3-epoxyhexane, 3-ethyl-2,3-epoxyoctane, epichlorhydrin, epibromohydrin, styrene oxide, glycidyl ether, methyl glycidyl ether, phenyl glycidyl ether, butyl glycidyl sulphide, glycidylmethyl sulphone, glycidyl methacrylate or acrylate, benzoate, acetate, octanoate, or sorbate, glycidyl allyl phthalate, phenyl-(p-octadecyloxybenzoyl) ethylene oxide and compounds of the formulae <FORM:0919067/IV(a)/1> Gas is formed by reaction of the polyisocyanate with the phosphorus compound, but as an additional foaming agent there can be used fluorochlorohydrocarbons; tertiary alcohols in the presence of strong acids; secondary alcohols alone or with acids; polycarboxylic acids, or anhydrides, dimethylol ureas, polymethylol phenols, formic acid or tetrahydroxymethylphosphonium chloride. As phosphorus acids there are listed, phosphoric, phosphorous, and hypophosphorous acids and a number of phosphonic, phosphinic, and phosphonous acids, primary and secondary phosphates and phosphites, and primary phosphonates and phosphonites. Specified fillers and additives are clay, calcium sulphate, ammonium phosphate, dyes, fibrous glass, asbestos or synthetic fibres. In examples foams are prepared by reacting (1) (A) a mixture of a trimethylolpropane-propylene oxide reaction product, a polyester from trimethylolpropane and 1,4,5,6,7,7-hexachlorobicyclo-(2.2.1)-5-heptene-2,3-dicarboxylic acid and mono- and di-butyl phosphates with (B) a solution of trichlorofluoromethane and a reaction product of 1,4,5,6,7,7-hexachlorobicyclo-(2.2.1)-5-heptene-2,3-dicarboxylic acid and toluene 2.4- and 2.6-diisocyanates; (2) similar reactants but with the use of phosphorous acid in place of the butyl phosphates; (3) a mixture of a glycerine/adipic acid/1,4,5,6,7,7-hexachlorobicyclo-(2.2.1)-5-heptene-2, 3-dicarboxylic acid polyester, a trimethylolpropane/adipic acid polyester mono- and dibutyl phosphates and trichlorofluoromethane with a semi-prepolymer from a portion of the chlorine containing polyester and toluene diisocyanates; (4) an adipic acid/phthalic anhydride/trimethylolpropane polyester with other reactants and procedures as specified in Example (3). In other examples the procedure of Example (1) is followed using as the phosphorus compound (8) phosphoric acid, (9) phenylphosphonic acid, (10) dimethylphosphinic acid, (11) methylphosphonous acid, (12) phenylphosphoric acid, (13) methyl ethyl phosphoric acid, (14) butyl phosphorus acid. Specification 873,974 is referred to.ALSO:A process for the production of a fire-resistant cellular reaction product comprises reacting (1) a hydroxylcontaining polymer having a hydroxyl number of between about 25 and 900, (2) an organic polyisocyanate, and (3) from 5 to 30% by weight, based on the weight of the hydroxyl-containing polymer of a phosphorus acid or a partially esterified phosphorous acid or mixtures thereof. The hydroxyl-containing polymer may be a polyester, polyether or mixtures thereof. As a modification an organic diisocyanate is first reacted with a polyester to form a prepolymer and this is then reacted with a polyether and/or further polyester and with the phosphorous acid or partially esterified phosphorous acid. Components are listed for the preparation of the polyesters and include Diels-Alderd adducts of a bexahalocyclopentadiene with a polycarboxylic acid or with a polyhydric alcohol. Compounds list for reaction with polyalcohols or polycarboxylic acids in the preparation of polyethers include epoxides containing halogen, ether, sulphide, sulphone, ester, amino and sulphonamide groups. Gas is formed by the reaction of the polyisocyanate and the phosphorus compound, but as an additional foaming agent there can be used fluorochlorohydrocarbons; tertiary alcohols in the presence of p strong acids; secondary alcohols above or with acids; polycarboxylic acids or anhydrides, dimethylol ureas, polymethylol phenols, formic acid or tetrahydroxymethyl phosphorium chloride. As phosphorous acids these are listed phosphoric, phosphorous and hypophosphorous acids and a number of phosphonic, phosphinic and phosphonous acids primary and secondary phosphates and phosphites, and primary phosphonates and phosphonites. Specified fillers and additives are clay, calcium sulphate, ammonium phosphate, dyes, fibrous glass, asbestos or synthetic fibres. In Example (1) a foam is prepared (1) by reacting (A) a mixture of trimethylalpropane-propylene oxide reaction product, a polyester from trimethylolpropane and 1, 4, 5, 6, 7, 7-hexachlorobicyilo -(2, 2,1)-5-heptene -2, 3-decarboxylic acid and mono-and dibutyl phosphates with (B) a solution of trichlorofluoromethane and a reaction product of 1, 4, 5, 6, 7, 7- hexachlorobicyclo- (2.2.1)-5- heptene -2, 3- dicarboxylic acid and toluene -2, 4-and 2, 6- diisocyanates. In other examples the procedure of (1) is followed using as the phosphorus compound (8) phosphoric acid, (9) phenylphosphoric acid, (10) dimethylphosphinic acid, (11) methylphosphorous acid, (12) phenyl phosphoric acid, (13) methyl ethyl phosphoric acid, (14) butyl phosphorous acid. Specification 873,974 is referred to.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2489761A GB919067A (en) | 1961-07-10 | 1961-07-10 | Phosphorus containing polyurethane foams |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2489761A GB919067A (en) | 1961-07-10 | 1961-07-10 | Phosphorus containing polyurethane foams |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB919067A true GB919067A (en) | 1963-02-20 |
Family
ID=10218992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2489761A Expired GB919067A (en) | 1961-07-10 | 1961-07-10 | Phosphorus containing polyurethane foams |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB919067A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3385801A (en) * | 1964-05-05 | 1968-05-28 | Monsanto Co | Flame-resistant polyurethanes |
| US3424701A (en) * | 1967-08-29 | 1969-01-28 | Hooker Chemical Corp | Polyurethane compositions |
| DE1301119B (en) * | 1964-08-06 | 1969-08-14 | Albright & Wilson Mfg Ltd | Process for the production of polyurethanes |
| US3498936A (en) * | 1964-05-27 | 1970-03-03 | Hooker Chemical Corp | Hydroxyalkylated phenol-sulfur halide resins and polyurethanes containing same |
| US3791914A (en) * | 1972-01-26 | 1974-02-12 | Ppg Industries Inc | Laminated glass articles |
| US4666967A (en) * | 1985-01-23 | 1987-05-19 | Ciba-Geigy Corporation | Flame retardants for polyurethanes |
| EP0853073A4 (en) * | 1995-09-27 | 1998-11-25 | Sanyo Chemical Ind Ltd | INORGANIC-ORGANIC COMPOSITE FOAM AND MANUFACTURING METHOD THEREOF |
| US6610756B1 (en) | 1997-07-08 | 2003-08-26 | Sanyo Checmical Industries, Ltd. | Inorganic/organic composite foam and process for producing the same |
| CN113698568A (en) * | 2021-07-20 | 2021-11-26 | 佳化化学科技发展(上海)有限公司 | Combined polyether, polyisocyanurate foam, preparation method and application thereof |
-
1961
- 1961-07-10 GB GB2489761A patent/GB919067A/en not_active Expired
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3385801A (en) * | 1964-05-05 | 1968-05-28 | Monsanto Co | Flame-resistant polyurethanes |
| US3498936A (en) * | 1964-05-27 | 1970-03-03 | Hooker Chemical Corp | Hydroxyalkylated phenol-sulfur halide resins and polyurethanes containing same |
| DE1301119B (en) * | 1964-08-06 | 1969-08-14 | Albright & Wilson Mfg Ltd | Process for the production of polyurethanes |
| US3424701A (en) * | 1967-08-29 | 1969-01-28 | Hooker Chemical Corp | Polyurethane compositions |
| US3791914A (en) * | 1972-01-26 | 1974-02-12 | Ppg Industries Inc | Laminated glass articles |
| US4666967A (en) * | 1985-01-23 | 1987-05-19 | Ciba-Geigy Corporation | Flame retardants for polyurethanes |
| EP0853073A4 (en) * | 1995-09-27 | 1998-11-25 | Sanyo Chemical Ind Ltd | INORGANIC-ORGANIC COMPOSITE FOAM AND MANUFACTURING METHOD THEREOF |
| US6313186B1 (en) | 1995-09-27 | 2001-11-06 | Sanyo Chemical Industries, Ltd. | Inorganic-organic composite foam and process for the production thereof |
| US6610756B1 (en) | 1997-07-08 | 2003-08-26 | Sanyo Checmical Industries, Ltd. | Inorganic/organic composite foam and process for producing the same |
| CN113698568A (en) * | 2021-07-20 | 2021-11-26 | 佳化化学科技发展(上海)有限公司 | Combined polyether, polyisocyanurate foam, preparation method and application thereof |
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