BG63343B1 - Полиетерполиол, метод за получаването му, полиетерполиолна смес, твърд пенополиуретан и използването му - Google Patents

Полиетерполиол, метод за получаването му, полиетерполиолна смес, твърд пенополиуретан и използването му Download PDF

Info

Publication number: BG63343B1
Authority: BG; Bulgaria
Prior art keywords: polyol; range; polyether polyol; mixture; polyurethane foam
Prior art date: 1995-12-07

Application number

BG101034A

Other languages

Bulgarian (bg)

English (en)

Other versions

BG101034A (en

Inventor

Thomas Broennum

Parminder SANGHA

Johannes STEINMETZ

Original Assignee

Shell Internationale Research Maatschappij B.V.

Priority date (The priority date 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 date listed.)

1995-12-07

Filing date

1996-12-05

Publication date

2001-10-31

1996-12-05 Application filed by Shell Internationale Research Maatschappij B.V. filed Critical Shell Internationale Research Maatschappij B.V.

1997-09-30 Publication of BG101034A publication Critical patent/BG101034A/xx

2001-10-31 Publication of BG63343B1 publication Critical patent/BG63343B1/bg

Links

239000006260 foam Substances 0.000 title claims abstract description 16
238000002360 preparation method Methods 0.000 title claims abstract description 11
229920002635 polyurethane Polymers 0.000 title abstract description 8
239000004814 polyurethane Substances 0.000 title abstract description 8
229920005862 polyol Polymers 0.000 claims abstract description 84
150000003077 polyols Chemical class 0.000 claims abstract description 80
239000000203 mixture Substances 0.000 claims abstract description 52
239000005056 polyisocyanate Substances 0.000 claims abstract description 23
229920001228 polyisocyanate Polymers 0.000 claims abstract description 23
229920005903 polyol mixture Polymers 0.000 claims abstract description 23
125000003118 aryl group Chemical group 0.000 claims abstract description 22
125000001931 aliphatic group Chemical group 0.000 claims abstract description 20
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 18
239000003153 chemical reaction reagent Substances 0.000 claims abstract description 16
125000002723 alicyclic group Chemical group 0.000 claims abstract description 12
238000000034 method Methods 0.000 claims abstract description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 11
239000012948 isocyanate Substances 0.000 claims abstract description 11
150000002513 isocyanates Chemical class 0.000 claims abstract description 11
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 10
239000001257 hydrogen Substances 0.000 claims abstract description 10
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract description 5
125000000217 alkyl group Chemical group 0.000 claims abstract description 3
239000004721 Polyphenylene oxide Substances 0.000 claims description 53
229920000570 polyether Polymers 0.000 claims description 53
229920005830 Polyurethane Foam Polymers 0.000 claims description 45
239000011496 polyurethane foam Substances 0.000 claims description 45
239000007787 solid Substances 0.000 claims description 30
150000001875 compounds Chemical class 0.000 claims description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
230000008961 swelling Effects 0.000 claims description 12
239000003795 chemical substances by application Substances 0.000 claims description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
125000002947 alkylene group Chemical group 0.000 claims description 8
238000005187 foaming Methods 0.000 claims description 7
RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 6
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 3
238000009413 insulation Methods 0.000 claims description 3
238000006243 chemical reaction Methods 0.000 abstract description 11
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 28
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 22
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 21
239000003054 catalyst Substances 0.000 description 18
238000010438 heat treatment Methods 0.000 description 12
206010042674 Swelling Diseases 0.000 description 11
238000009472 formulation Methods 0.000 description 11
-1 polypropylene Polymers 0.000 description 11
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical class C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 10
150000001298 alcohols Chemical class 0.000 description 10
239000011810 insulating material Substances 0.000 description 10
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 7
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 7
239000000047 product Substances 0.000 description 7
150000003254 radicals Chemical class 0.000 description 7
239000000600 sorbitol Substances 0.000 description 7
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
150000001335 aliphatic alkanes Chemical class 0.000 description 6
125000004435 hydrogen atom Chemical class [H]* 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
238000007906 compression Methods 0.000 description 5
230000006835 compression Effects 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
229910000831 Steel Inorganic materials 0.000 description 4
230000032683 aging Effects 0.000 description 4
PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 4
239000010959 steel Substances 0.000 description 4
SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 3
SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
229930006000 Sucrose Natural products 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
239000001569 carbon dioxide Substances 0.000 description 3
229910002092 carbon dioxide Inorganic materials 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
150000008282 halocarbons Chemical class 0.000 description 3
239000012774 insulation material Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000005720 sucrose Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
BHNZEZWIUMJCGF-UHFFFAOYSA-N 1-chloro-1,1-difluoroethane Chemical group CC(F)(F)Cl BHNZEZWIUMJCGF-UHFFFAOYSA-N 0.000 description 2
229930185605 Bisphenol Natural products 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
208000000474 Poliomyelitis Diseases 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
229910000272 alkali metal oxide Inorganic materials 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
150000001734 carboxylic acid salts Chemical class 0.000 description 2
235000019820 disodium diphosphate Nutrition 0.000 description 2
GYQBBRRVRKFJRG-UHFFFAOYSA-L disodium pyrophosphate Chemical compound [Na+].[Na+].OP([O-])(=O)OP(O)([O-])=O GYQBBRRVRKFJRG-UHFFFAOYSA-L 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000012467 final product Substances 0.000 description 2
239000004872 foam stabilizing agent Substances 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
230000003472 neutralizing effect Effects 0.000 description 2
125000002524 organometallic group Chemical group 0.000 description 2
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
230000003578 releasing effect Effects 0.000 description 2
150000003512 tertiary amines Chemical class 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 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
230000004580 weight loss Effects 0.000 description 2
SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
ICLCCFKUSALICQ-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanato-3-methylphenyl)-2-methylbenzene Chemical compound C1=C(N=C=O)C(C)=CC(C=2C=C(C)C(N=C=O)=CC=2)=C1 ICLCCFKUSALICQ-UHFFFAOYSA-N 0.000 description 1
RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 description 1
SODXZRVMVYFUDO-UHFFFAOYSA-N 2-(2-hydroxypropoxy)propan-1-ol;propane-1,2,3-triol Chemical compound OCC(O)CO.CC(O)COC(C)CO SODXZRVMVYFUDO-UHFFFAOYSA-N 0.000 description 1
QZWKEPYTBWZJJA-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine-4,4'-diisocyanate Chemical compound C1=C(N=C=O)C(OC)=CC(C=2C=C(OC)C(N=C=O)=CC=2)=C1 QZWKEPYTBWZJJA-UHFFFAOYSA-N 0.000 description 1
VIVLBCLZNBHPGE-UHFFFAOYSA-N 3-methoxy-n,n-dimethylpropan-1-amine Chemical compound COCCCN(C)C VIVLBCLZNBHPGE-UHFFFAOYSA-N 0.000 description 1
229910015900 BF3 Inorganic materials 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
235000014755 Eruca sativa Nutrition 0.000 description 1
244000024675 Eruca sativa Species 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
239000002841 Lewis acid Substances 0.000 description 1
AKTQSHIRSZYKJS-UHFFFAOYSA-N N-methylmethanamine Chemical compound CNC.CNC AKTQSHIRSZYKJS-UHFFFAOYSA-N 0.000 description 1
229920000265 Polyparaphenylene Polymers 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical group [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000002585 base Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
230000000593 degrading effect Effects 0.000 description 1
RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical compound CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-UHFFFAOYSA-L 0.000 description 1
229940105990 diglycerin Drugs 0.000 description 1
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
238000009826 distribution Methods 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
229920001903 high density polyethylene Polymers 0.000 description 1
239000004700 high-density polyethylene Substances 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
DSSXKBBEJCDMBT-UHFFFAOYSA-M lead(2+);octanoate Chemical compound [Pb+2].CCCCCCCC([O-])=O DSSXKBBEJCDMBT-UHFFFAOYSA-M 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
PGYPOBZJRVSMDS-UHFFFAOYSA-N loperamide hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)N(C)C)CCN(CC1)CCC1(O)C1=CC=C(Cl)C=C1 PGYPOBZJRVSMDS-UHFFFAOYSA-N 0.000 description 1
XFLSMWXCZBIXLV-UHFFFAOYSA-N n,n-dimethyl-2-(4-methylpiperazin-1-yl)ethanamine Chemical compound CN(C)CCN1CCN(C)CC1 XFLSMWXCZBIXLV-UHFFFAOYSA-N 0.000 description 1
GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
UIEKYBOPAVTZKW-UHFFFAOYSA-L naphthalene-2-carboxylate;nickel(2+) Chemical compound [Ni+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 UIEKYBOPAVTZKW-UHFFFAOYSA-L 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
150000002902 organometallic compounds Chemical class 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035939 shock Effects 0.000 description 1
229920005573 silicon-containing polymer Polymers 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
230000008646 thermal stress Effects 0.000 description 1
238000002411 thermogravimetry Methods 0.000 description 1
230000000930 thermomechanical effect Effects 0.000 description 1
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- 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
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- 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
- C08G18/487—Polyethers containing cyclic groups
- C08G18/4879—Polyethers containing cyclic groups containing aromatic groups
- 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
- C08G2110/0025—Foam properties rigid
- 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

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)
Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Polyethers (AREA)

BG101034A 1995-12-07 1996-12-05 Полиетерполиол, метод за получаването му, полиетерполиолна смес, твърд пенополиуретан и използването му BG63343B1 (bg)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP95203399		1995-12-07

Publications (2)

Publication Number	Publication Date
BG101034A BG101034A (en)	1997-09-30
BG63343B1 true BG63343B1 (bg)	2001-10-31

Family

ID=8220917

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BG101034A BG63343B1 (bg)	1995-12-07	1996-12-05	Полиетерполиол, метод за получаването му, полиетерполиолна смес, твърд пенополиуретан и използването му

Country Status (21)

Country	Link
US (1)	US5824714A (de)
EP (1)	EP0778302B1 (de)
JP (1)	JPH09176302A (de)
KR (1)	KR100467382B1 (de)
CN (1)	CN1082516C (de)
AT (1)	ATE216710T1 (de)
BG (1)	BG63343B1 (de)
CA (1)	CA2192146C (de)
CZ (1)	CZ291241B6 (de)
DE (1)	DE69620850T2 (de)
DK (1)	DK0778302T3 (de)
ES (1)	ES2176401T3 (de)
HU (1)	HU218088B (de)
NO (1)	NO311694B1 (de)
PL (1)	PL186571B1 (de)
PT (1)	PT778302E (de)
RU (1)	RU2177960C2 (de)
SG (1)	SG48495A1 (de)
SK (1)	SK281277B6 (de)
TW (1)	TW505672B (de)
UA (1)	UA52585C2 (de)

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EP1260529A1 (de)	2001-05-21	2002-11-27	Borealis Technology OY	Propylenpolymere mit verbesserten Eigenschaften
US6706776B2 (en) *	2002-06-18	2004-03-16	Bayer Corporation	Syntactic foams with improved water resistance, long pot life and short demolding times
DE102004028769A1 (de) *	2004-06-16	2005-12-29	Basf Ag	Verfahren zur Herstellung von Polyetheralkoholen und Polyurethanen
EP1840143A1 (de)	2006-03-29	2007-10-03	Sika Technology AG	Wässriger einkomponentiger Dispersionsprimer für das Verkleben von Kunststofffolien mittels Dispersionsklebstoffen
US7538162B2 (en) *	2006-06-23	2009-05-26	Bayer Materialscience Llc	Process for the production of polyoxyalkylene containing polyols from phenol condensation products
CN101161699B (zh) *	2006-10-09	2011-09-21	李颂兵	一种用于制备无氟聚氨酯硬质泡沫塑料的聚醚多元醇及其制取方法
DE102006048288A1 (de) *	2006-10-12	2008-04-17	Bayer Materialscience Ag	Polyesterpolyole, Verfahren zu ihrer Herstellung und ihre Verwendung
RU2339663C1 (ru) *	2007-06-05	2008-11-27	Федеральное казенное предприятие (ФКП) "Пермский пороховой завод"	Полиоловая композиция для получения жестких пенополиуретанов теплоизоляционного назначения
CN102287049B (zh) *	2011-05-26	2012-12-05	昆明二建建设（集团）有限公司	防腐抗渗保温屋面的施工方法
WO2020160206A1 (en) *	2019-01-31	2020-08-06	Dow Global Technologies Llc	Isocyanate reactive compositions
CN113773484A (zh) *	2021-09-10	2021-12-10	山东一诺威新材料有限公司	高抗压缩强度矿用聚醚多元醇的制备方法

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1996
- 1996-12-04 RU RU96122861/04A patent/RU2177960C2/ru not_active IP Right Cessation
- 1996-12-04 CZ CZ19963548A patent/CZ291241B6/cs not_active IP Right Cessation
- 1996-12-05 PL PL96317340A patent/PL186571B1/pl not_active IP Right Cessation
- 1996-12-05 BG BG101034A patent/BG63343B1/bg unknown
- 1996-12-05 CA CA002192146A patent/CA2192146C/en not_active Expired - Fee Related
- 1996-12-05 DK DK96203440T patent/DK0778302T3/da active
- 1996-12-05 AT AT96203440T patent/ATE216710T1/de not_active IP Right Cessation
- 1996-12-05 ES ES96203440T patent/ES2176401T3/es not_active Expired - Lifetime
- 1996-12-05 HU HU9603358A patent/HU218088B/hu not_active IP Right Cessation
- 1996-12-05 UA UA96124552A patent/UA52585C2/uk unknown
- 1996-12-05 PT PT96203440T patent/PT778302E/pt unknown
- 1996-12-05 JP JP8339135A patent/JPH09176302A/ja active Pending
- 1996-12-05 NO NO19965210A patent/NO311694B1/no unknown
- 1996-12-05 SK SK1557-96A patent/SK281277B6/sk unknown
- 1996-12-05 SG SG1996011539A patent/SG48495A1/en unknown
- 1996-12-05 EP EP96203440A patent/EP0778302B1/de not_active Expired - Lifetime
- 1996-12-05 DE DE69620850T patent/DE69620850T2/de not_active Expired - Fee Related
- 1996-12-06 CN CN96117276A patent/CN1082516C/zh not_active Expired - Fee Related
- 1996-12-06 KR KR1019960062465A patent/KR100467382B1/ko not_active Expired - Fee Related
- 1996-12-09 US US08/762,811 patent/US5824714A/en not_active Expired - Fee Related
1997
- 1997-01-24 TW TW086100794A patent/TW505672B/zh not_active IP Right Cessation

Also Published As

Publication number	Publication date
CN1157833A (zh)	1997-08-27
KR100467382B1 (ko)	2005-10-19
DE69620850D1 (de)	2002-05-29
TW505672B (en)	2002-10-11
CZ354896A3 (en)	1997-08-13
UA52585C2 (uk)	2003-01-15
RU2177960C2 (ru)	2002-01-10
NO311694B1 (no)	2002-01-07
NO965210D0 (no)	1996-12-05
PT778302E (pt)	2002-08-30
EP0778302B1 (de)	2002-04-24
CZ291241B6 (cs)	2003-01-15
SG48495A1 (en)	1998-04-17
ES2176401T3 (es)	2002-12-01
PL317340A1 (en)	1997-06-09
DE69620850T2 (de)	2002-10-10
HU218088B (hu)	2000-05-28
SK281277B6 (sk)	2001-02-12
JPH09176302A (ja)	1997-07-08
US5824714A (en)	1998-10-20
BG101034A (en)	1997-09-30
CN1082516C (zh)	2002-04-10
PL186571B1 (pl)	2004-01-30
ATE216710T1 (de)	2002-05-15
HU9603358D0 (en)	1997-01-28
HUP9603358A3 (en)	1998-03-02
CA2192146C (en)	2005-08-02
CA2192146A1 (en)	1997-06-08
NO965210L (no)	1997-06-09
KR970042643A (ko)	1997-07-24
EP0778302A1 (de)	1997-06-11
SK155796A3 (en)	1998-01-14
DK0778302T3 (da)	2002-08-19
HUP9603358A2 (en)	1997-12-29

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