GB1164997A - Improvements in Polyether Polyols and Polyurethanes Derived therefrom - Google Patents
Improvements in Polyether Polyols and Polyurethanes Derived therefromInfo
- Publication number
- GB1164997A GB1164997A GB5012665A GB5012665A GB1164997A GB 1164997 A GB1164997 A GB 1164997A GB 5012665 A GB5012665 A GB 5012665A GB 5012665 A GB5012665 A GB 5012665A GB 1164997 A GB1164997 A GB 1164997A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyether polyols
- mixture
- functionality
- polyol
- polyether
- 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
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
- 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
- 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
- C08G18/4829—Polyethers containing at least three hydroxy 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
- C08G18/56—Polyacetals
-
- 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
- C08G4/00—Condensation polymers of aldehydes or ketones with polyalcohols; Addition polymers of heterocyclic oxygen compounds containing in the ring at least once the grouping —O—C—O—
-
- 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
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
Abstract
1,164,997. Acetals of polyether polyols. B.P. CHEMICALS (U.K.) Ltd. 17 Nov., 1966 [25 Nov., 1965], No. 50126/65. Heading C2C. [Also in Division C3] Novel polyether polyols having a functionality of at least 4 and containing at least 1 but not more than 3 acetal links between branch points in the molecule are prepared by reaction of a polyether polyol having a functionality of at least 3 and an aldehyde under acidic conditions, whereby at least 0À5 but not more than 0À75 mole of aldehyde reacts for each mole of polyol present. The invention also comprises novel mixtures of polyether polyols having an average functionality greater than 3, at least one of the polyether polyols in the mixture having a functionality of at least 4 and containing 1 or more acetal links between branch points in its molecule, and the mixture as a whole containing an average of not more than 3 acetal links per molecule, which are prepared by reaction under acidic conditions of a polyether polyol having a functionality of at least 3, a mixture of polyether polyols or a mixture of one or more polyether polyols with a polyol which is not a polyether polyol but which contains at least 4 carbon atoms between any 2 of its hydroxyl groups, any such mixture having an average functionality greater than 2À25 whereby not more than 0À75 mole of the aldehyde reacts for each mole of polyol initially present, but sufficient aldehyde reacts to raise the functionality of the mixture to more than 3. Suitable polyether polyols for use as starting materials are the condensation products of ethylene oxide and/or 1,2-propylene oxide with glycerol, trimethylolpropane, 1,3,5-trihydroxycyclohexane, pentaerythritrol, sorbitol and sucrose, and mixtures thereof with each other and with polyoxyalkylene glycols. Suitable polyols which are not polyether polyols are diethylene and dipropylene glycols, tetramethylene and pentamethylene glycols, 1,4- dihydroxy- and dimethylol-cyclohexanes and bis-(2-hydroxyalkyl)-ethers of dihydroxy aromatic compounds. Specified aldehydes are aliphatic aldehydes containing up to 4 carbon atoms, especially formaldehyde, and also benzaldehyde and glyoxal. The resulting polyether polyols preferably have hydroxyl numbers between 30 and 70 mg. KOH per gram and may be reacted with ethylene oxide and/or propylene oxide to reduce the hydroxyl numbers to this range.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5012665A GB1164997A (en) | 1965-11-25 | 1965-11-25 | Improvements in Polyether Polyols and Polyurethanes Derived therefrom |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5012665A GB1164997A (en) | 1965-11-25 | 1965-11-25 | Improvements in Polyether Polyols and Polyurethanes Derived therefrom |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1164997A true GB1164997A (en) | 1969-09-24 |
Family
ID=10454748
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5012665A Expired GB1164997A (en) | 1965-11-25 | 1965-11-25 | Improvements in Polyether Polyols and Polyurethanes Derived therefrom |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1164997A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996000253A1 (en) * | 1994-06-23 | 1996-01-04 | The Dow Chemical Company | A surface active composition containing an acetal or ketal adduct |
WO2014095679A1 (en) | 2012-12-21 | 2014-06-26 | Bayer Materialscience Ag | Nco-modified polyoxymethylene block copolymers |
WO2016112274A1 (en) * | 2015-01-08 | 2016-07-14 | Dow Global Technologies Llc | Polyether-acetal polyol compositions |
US9469715B2 (en) | 2012-12-21 | 2016-10-18 | Covestro Deutschland Ag | Method for producing formaldehyde/CO2 copolymers |
US9688814B2 (en) | 2012-12-21 | 2017-06-27 | Covestro Deutschland Ag | Functionalized polyoxymethylene block copolymers |
US9790328B2 (en) | 2013-06-13 | 2017-10-17 | Covestro Deutschland Ag | Polyethercarbonate-polyoxymethylene block copolymers |
-
1965
- 1965-11-25 GB GB5012665A patent/GB1164997A/en not_active Expired
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996000253A1 (en) * | 1994-06-23 | 1996-01-04 | The Dow Chemical Company | A surface active composition containing an acetal or ketal adduct |
CN104918974B (en) * | 2012-12-21 | 2017-10-13 | 科思创德国股份有限公司 | The polyformaldehyde block copolymer that NCO is modified |
CN104918974A (en) * | 2012-12-21 | 2015-09-16 | 拜耳材料科技股份有限公司 | Nco-modified polyoxymethylene block copolymers |
US9469715B2 (en) | 2012-12-21 | 2016-10-18 | Covestro Deutschland Ag | Method for producing formaldehyde/CO2 copolymers |
US9534090B2 (en) | 2012-12-21 | 2017-01-03 | Covestro Deutschland Ag | NCO-modified polyoxymethylene block copolymers |
US9688814B2 (en) | 2012-12-21 | 2017-06-27 | Covestro Deutschland Ag | Functionalized polyoxymethylene block copolymers |
WO2014095679A1 (en) | 2012-12-21 | 2014-06-26 | Bayer Materialscience Ag | Nco-modified polyoxymethylene block copolymers |
US9790328B2 (en) | 2013-06-13 | 2017-10-17 | Covestro Deutschland Ag | Polyethercarbonate-polyoxymethylene block copolymers |
WO2016112274A1 (en) * | 2015-01-08 | 2016-07-14 | Dow Global Technologies Llc | Polyether-acetal polyol compositions |
CN107108846A (en) * | 2015-01-08 | 2017-08-29 | 陶氏环球技术有限责任公司 | Polyetheracetal glycol composition |
KR20170103818A (en) * | 2015-01-08 | 2017-09-13 | 다우 글로벌 테크놀로지스 엘엘씨 | Polyether-acetal polyol compositons |
US10435502B2 (en) | 2015-01-08 | 2019-10-08 | Dow Global Technologies Llc | Polyether-acetal polyol compositions |
CN107108846B (en) * | 2015-01-08 | 2020-07-10 | 陶氏环球技术有限责任公司 | Polyether-acetal polyol compositions |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2786081A (en) | Acetal condensation products | |
GB1494538A (en) | Stabilised polyalkylene polyols and polyurethane foams prepared therefrom | |
GB1164997A (en) | Improvements in Polyether Polyols and Polyurethanes Derived therefrom | |
ES259814A1 (en) | Hydroxy-containing hemi-acetals, their preparation and use | |
GB1125046A (en) | Starch-based polyhydroxy-polyoxyalkylene ethers | |
GB1529475A (en) | Process for the preparation of etherified acetal polymers | |
GB850178A (en) | Improvements in the manufacture of polyformal materials | |
GB956586A (en) | Intermediates and polyurethane plastics | |
GB1039936A (en) | Process for the manufacture of copolymers of acetals | |
FR2240283A1 (en) | Borate ester brake fluids for vehicles - derived from glycols, triols and/or glycol, mono-ethers, with reduced water absorption | |
GB1488108A (en) | Polyglycol ether derivatives and wetting washing and cleansing compositions containing them | |
GB1100404A (en) | Improvements in or relating to the manufacture of polyols from epoxides | |
GB1384957A (en) | Method of preparing polyoxyalkylene glycols and their monoethers | |
SE7508823L (en) | KIT FOR CONTINUOUS PREPARATION OF TRIMETHYLOLAL CHANNEL LYLETHERS. | |
GB1129028A (en) | New compounds containing oxetane groups, a process for their preparation, and use | |
US3388169A (en) | Stabilization of polyoxyalkylene compounds | |
ES409466A1 (en) | Adhesive solutions | |
FR2160976A1 (en) | Pure crystalline ethers - from phenol and alkyl polyols using azeotropic distn | |
US3322740A (en) | Alkylene oxide-polyol polyether modified acetal resins | |
GB1169272A (en) | Polyglycols and Photographic Compositions containing them | |
KR840001942A (en) | Process for preparing glycol ether | |
JPS5589333A (en) | Polyol for raw material of polyurethanes and its production | |
GB1384949A (en) | Halogenated methylol phenols | |
GB1066326A (en) | Process for the manufacture of polyethers | |
GB1451720A (en) | Mixtures of methylol monoalkyl ureas and their butyl ethers |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |