GB1480949A - Preparation of flexible polyurethane foams - Google Patents
Preparation of flexible polyurethane foamsInfo
- Publication number
- GB1480949A GB1480949A GB52014/74A GB5201474A GB1480949A GB 1480949 A GB1480949 A GB 1480949A GB 52014/74 A GB52014/74 A GB 52014/74A GB 5201474 A GB5201474 A GB 5201474A GB 1480949 A GB1480949 A GB 1480949A
- Authority
- GB
- United Kingdom
- Prior art keywords
- stannous
- primary
- content
- propylene oxide
- glycerol
- 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
- 229920005830 Polyurethane Foam Polymers 0.000 title abstract 3
- 239000011496 polyurethane foam Substances 0.000 title abstract 3
- -1 ether polyol Chemical class 0.000 abstract 6
- 229920005862 polyol Polymers 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 3
- 239000005056 polyisocyanate Substances 0.000 abstract 3
- 229920001228 polyisocyanate Polymers 0.000 abstract 3
- 229920001296 polysiloxane Polymers 0.000 abstract 3
- CESZUODSLPRJDU-UHFFFAOYSA-N 2-methyloxirane;oxirane;propane-1,2,3-triol Chemical compound C1CO1.CC1CO1.OCC(O)CO CESZUODSLPRJDU-UHFFFAOYSA-N 0.000 abstract 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 abstract 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- 239000006260 foam Substances 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 229940049964 oleate Drugs 0.000 abstract 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-M oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC([O-])=O ZQPPMHVWECSIRJ-KTKRTIGZSA-M 0.000 abstract 2
- 150000003077 polyols Chemical class 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 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 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- OSNILPMOSNGHLC-UHFFFAOYSA-N 1-[4-methoxy-3-(piperidin-1-ylmethyl)phenyl]ethanone Chemical compound COC1=CC=C(C(C)=O)C=C1CN1CCCCC1 OSNILPMOSNGHLC-UHFFFAOYSA-N 0.000 abstract 1
- YTZRFUSYPGFDNC-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;2-methyloxirane;oxirane Chemical compound C1CO1.CC1CO1.CCC(CO)(CO)CO YTZRFUSYPGFDNC-UHFFFAOYSA-N 0.000 abstract 1
- BJUPZVQSAAGZJL-UHFFFAOYSA-N 2-methyloxirane;propane-1,2,3-triol Chemical compound CC1CO1.OCC(O)CO BJUPZVQSAAGZJL-UHFFFAOYSA-N 0.000 abstract 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-M 9-cis,12-cis-Octadecadienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O OYHQOLUKZRVURQ-HZJYTTRNSA-M 0.000 abstract 1
- 239000005995 Aluminium silicate Substances 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- 229910010413 TiO 2 Inorganic materials 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- PZZYQPZGQPZBDN-UHFFFAOYSA-N aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 abstract 1
- 229910000323 aluminium silicate Inorganic materials 0.000 abstract 1
- 235000012211 aluminium silicate Nutrition 0.000 abstract 1
- 229910000410 antimony oxide Inorganic materials 0.000 abstract 1
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract 1
- 235000010216 calcium carbonate Nutrition 0.000 abstract 1
- 239000000378 calcium silicate Substances 0.000 abstract 1
- 229910052918 calcium silicate Inorganic materials 0.000 abstract 1
- 235000012241 calcium silicate Nutrition 0.000 abstract 1
- 239000001175 calcium sulphate Substances 0.000 abstract 1
- 235000011132 calcium sulphate Nutrition 0.000 abstract 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 abstract 1
- 239000006229 carbon black Substances 0.000 abstract 1
- ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 abstract 1
- PNOXNTGLSKTMQO-UHFFFAOYSA-L diacetyloxytin Chemical compound CC(=O)O[Sn]OC(C)=O PNOXNTGLSKTMQO-UHFFFAOYSA-L 0.000 abstract 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000001023 inorganic pigment Substances 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 abstract 1
- 235000013980 iron oxide Nutrition 0.000 abstract 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 abstract 1
- 229940070765 laurate Drugs 0.000 abstract 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 abstract 1
- 229940049918 linoleate Drugs 0.000 abstract 1
- 239000000391 magnesium silicate Substances 0.000 abstract 1
- 229910052919 magnesium silicate Inorganic materials 0.000 abstract 1
- 235000019792 magnesium silicate Nutrition 0.000 abstract 1
- ZADYMNAVLSWLEQ-UHFFFAOYSA-N magnesium;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[Mg+2].[Si+4] ZADYMNAVLSWLEQ-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 abstract 1
- CYCFYXLDTSNTGP-UHFFFAOYSA-L octadecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CYCFYXLDTSNTGP-UHFFFAOYSA-L 0.000 abstract 1
- 150000002894 organic compounds Chemical class 0.000 abstract 1
- 239000012860 organic pigment Substances 0.000 abstract 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000377 silicon dioxide Substances 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
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/24—Catalysts containing metal compounds of tin
- C08G18/244—Catalysts containing metal compounds of tin tin salts of carboxylic acids
-
- 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
- Y10S521/914—Polyurethane cellular product formed from a polyol which has been derived from at least two 1,2 epoxides as reactants
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US421088A US3887505A (en) | 1973-12-03 | 1973-12-03 | Preparation of low density flexible urethane foams with enhanced load-bearing properties |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1480949A true GB1480949A (en) | 1977-07-27 |
Family
ID=23669122
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB52014/74A Expired GB1480949A (en) | 1973-12-03 | 1974-12-02 | Preparation of flexible polyurethane foams |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3887505A (enExample) |
| BE (1) | BE822798A (enExample) |
| CA (1) | CA1033896A (enExample) |
| DE (1) | DE2455289A1 (enExample) |
| FR (1) | FR2253038B3 (enExample) |
| GB (1) | GB1480949A (enExample) |
| IT (1) | IT1023461B (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4101471A (en) * | 1975-12-18 | 1978-07-18 | M & T Chemicals Inc. | High resiliency foam with improved load bearing ability by use of organotin mercaptides |
| JPS583488B2 (ja) * | 1978-05-15 | 1983-01-21 | 株式会社ブリヂストン | 軟質ポリエ−テルポリウレタンフオ−ムの製造方法 |
| US4302552A (en) * | 1980-07-01 | 1981-11-24 | Nisshin Spinning Co., Ltd. | Microcellular polyurethane vibration isolator |
| EP0044481B2 (de) * | 1980-07-21 | 1987-03-11 | Mobay Chemical Corporation | Verfahren zur Herstellung elastischer geformter Gegenstände |
| DE3100977A1 (de) * | 1981-01-15 | 1982-08-05 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von gegebenenfalls geschaeumten polyurethanen |
| DE3126517A1 (de) * | 1981-07-04 | 1983-01-20 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von gegebenenfalls zellhaltigen polyurethan-elastomeren |
| US4607064A (en) * | 1983-05-16 | 1986-08-19 | The Dow Chemical Company | Polyurethane and urethane-modified isocyanurate foams and a polyol composition useful in their preparation |
| US4487854A (en) * | 1983-12-27 | 1984-12-11 | Basf Wyandotte Corporation | Polyoxyalkylene polyether polyols and polyurethane foams prepared therefrom |
| US4532262A (en) * | 1984-03-21 | 1985-07-30 | Gloskey Carl R | Process for the preparation of urethane foam |
| US4661529A (en) * | 1984-08-09 | 1987-04-28 | The Dow Chemical Company | Polyurethane and urethane-modified isocyanurate foams and a polyol composition useful in their preparation |
| US4600730A (en) * | 1984-12-19 | 1986-07-15 | Societe Chimique Des Charbonnages S.A. | Stable prepolymers of polyisocyanate with hydroxyl functions, a process for their manufacture and their application to the manufacture of polyurethanes |
| GB2185987B (en) * | 1986-01-31 | 1989-10-25 | Japan National Railway | Resilient coat for tie of direct-connection type track |
| US4950694A (en) * | 1989-06-29 | 1990-08-21 | Union Carbide Chemicals And Plastics Company Inc. | Preparation of polyurethane foams without using inert blowing agents |
| JP2014524965A (ja) | 2011-07-25 | 2014-09-25 | ノボマー， インコーポレイテッド | ポリウレタンに使用するための脂肪族ポリカーボネート |
| ES2752043T3 (es) | 2012-11-07 | 2020-04-02 | Saudi Aramco Tech Co | Composiciones de espuma de poliuretano de gran resistencia y métodos |
| US20160115288A1 (en) * | 2013-05-13 | 2016-04-28 | Novomer, Inc. | Co2 containing foams and related methods |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3398106A (en) * | 1960-04-26 | 1968-08-20 | Union Carbide Corp | Tin-containing catalyst for isocyanate reactions |
| US3332934A (en) * | 1965-05-21 | 1967-07-25 | Allied Chem | Trialkylolamine polyether polyols |
| US3595814A (en) * | 1968-11-14 | 1971-07-27 | Jefferson Chem Co Inc | Urethanes containing monocarbamate chain extenders |
-
1973
- 1973-12-03 US US421088A patent/US3887505A/en not_active Expired - Lifetime
-
1974
- 1974-11-15 CA CA213,899A patent/CA1033896A/en not_active Expired
- 1974-11-22 DE DE19742455289 patent/DE2455289A1/de not_active Withdrawn
- 1974-11-29 FR FR7439309A patent/FR2253038B3/fr not_active Expired
- 1974-11-29 IT IT54308/74A patent/IT1023461B/it active
- 1974-11-29 BE BE151028A patent/BE822798A/xx unknown
- 1974-12-02 GB GB52014/74A patent/GB1480949A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2253038A1 (enExample) | 1975-06-27 |
| FR2253038B3 (enExample) | 1977-08-26 |
| BE822798A (fr) | 1975-05-29 |
| IT1023461B (it) | 1978-05-10 |
| DE2455289A1 (de) | 1975-06-05 |
| US3887505A (en) | 1975-06-03 |
| CA1033896A (en) | 1978-06-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |