GB1108013A - Improvements in or relating to foamed polyurethanes - Google Patents
Improvements in or relating to foamed polyurethanesInfo
- Publication number
- GB1108013A GB1108013A GB19994/64A GB1999464A GB1108013A GB 1108013 A GB1108013 A GB 1108013A GB 19994/64 A GB19994/64 A GB 19994/64A GB 1999464 A GB1999464 A GB 1999464A GB 1108013 A GB1108013 A GB 1108013A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polyester
- agents
- phthalic anhydride
- phthalic
- groups
- 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
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
- C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain 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
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4291—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from polyester forming components containing monoepoxy compounds
-
- 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
- C08G2110/005—< 50kg/m3
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)
Abstract
Foamed polyurethanes are formed by reaction in presence of an inert liquid of low B.Pt. of an organic polyisocyanate with an OH-containing polyester having at least 3 isocyanate-reactive groups/molecule, more than 50 molar per cent of the acid residue in the polyester being phthalic or substituted phthalic acid residues, and the polyester being obtained by reacting phthalic anhydride or substituted phthalic anhydride with a polyhydric alcohol having at least 3 OH groups and with an alkylene oxide. Substituted phthalic anhydrides mentioned are tetrabromo- and tetrachloro-phthalic anhydride. Suitable polyhydric alcohols are glycerol, trimethylolmethane, trimethylolpropane, erythritol, pentaerythritol and methyl glycoside. Alkylene oxides mentioned are ethylene, 1,2-propylene, butylene, and epichlorohydrin. Any of the conventional di- or tri-isocyanates may be used. Preferred inert liquids are halogenated hydrocarbons. Water may be included as an additional gas generator. Plasticizers or flame-proofing agents, e.g. tris-b -chloroethyl phosphate may be included in the reaction mixture. If desired the polyester may be mixed with up to an equal weight of a polyether with at least 3 OH groups per molecule. Conventional catalysts, surface-active agents, cross-linking agents, foam-stabilizing agents, colouring matters, fillers, plasticizers and antioxidants may also be incorporated.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE663892D BE663892A (en) | 1964-05-13 | ||
GB19994/64A GB1108013A (en) | 1964-05-13 | 1964-05-13 | Improvements in or relating to foamed polyurethanes |
FR16990A FR1442569A (en) | 1964-05-13 | 1965-05-13 | Polyurethane foam manufacturing process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB19994/64A GB1108013A (en) | 1964-05-13 | 1964-05-13 | Improvements in or relating to foamed polyurethanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1108013A true GB1108013A (en) | 1968-03-27 |
Family
ID=10138563
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19994/64A Expired GB1108013A (en) | 1964-05-13 | 1964-05-13 | Improvements in or relating to foamed polyurethanes |
Country Status (2)
Country | Link |
---|---|
BE (1) | BE663892A (en) |
GB (1) | GB1108013A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3933700A (en) * | 1973-03-12 | 1976-01-20 | Standard Oil Company | Modified polyurethane foams containing imide groups |
DE2656600A1 (en) * | 1976-01-19 | 1977-07-28 | Upjohn Co | POLYISOCYANURATE |
US4246365A (en) | 1976-08-18 | 1981-01-20 | Bayer Aktiengesellschaft | Process for the production of plastics containing isocyanurate groups and urethane groups |
US6103822A (en) * | 1996-08-16 | 2000-08-15 | Inolex Investment Corporation | Polymeric acid functional polyols, polyurethanes and methods for making same |
WO2011000546A1 (en) * | 2009-07-01 | 2011-01-06 | Bayer Materialscience Ag | Method for the production of a polyurethane polymer comprising polyester polyols that contain terminal secondary hydroxyl groups |
CN102414239A (en) * | 2009-05-06 | 2012-04-11 | 拜尔材料科学股份公司 | Method for producing polyester polyols having secondary OH end groups |
WO2013024108A1 (en) | 2011-08-16 | 2013-02-21 | Bayer Intellectual Property Gmbh | Method for producing a polyurethane/polyisocyanurate rigid foam |
WO2013024107A1 (en) | 2011-08-16 | 2013-02-21 | Bayer Intellectual Property Gmbh | Process for producing a rigid polyurethane-polyisocyanurate foam |
WO2015091471A1 (en) | 2013-12-18 | 2015-06-25 | Bayer Materialscience Ag | Method for working up alkaline polyether polyols |
-
0
- BE BE663892D patent/BE663892A/xx unknown
-
1964
- 1964-05-13 GB GB19994/64A patent/GB1108013A/en not_active Expired
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3933700A (en) * | 1973-03-12 | 1976-01-20 | Standard Oil Company | Modified polyurethane foams containing imide groups |
DE2656600A1 (en) * | 1976-01-19 | 1977-07-28 | Upjohn Co | POLYISOCYANURATE |
US4246365A (en) | 1976-08-18 | 1981-01-20 | Bayer Aktiengesellschaft | Process for the production of plastics containing isocyanurate groups and urethane groups |
US6103822A (en) * | 1996-08-16 | 2000-08-15 | Inolex Investment Corporation | Polymeric acid functional polyols, polyurethanes and methods for making same |
CN102414239B (en) * | 2009-05-06 | 2014-01-29 | 拜尔材料科学股份公司 | Method for producing polyester polyols having secondary OH end groups |
CN102414239A (en) * | 2009-05-06 | 2012-04-11 | 拜尔材料科学股份公司 | Method for producing polyester polyols having secondary OH end groups |
CN102471444A (en) * | 2009-07-01 | 2012-05-23 | 拜尔材料科学股份公司 | Process for preparing polyurethane polymers comprising polyester polyols having secondary hydroxyl end groups |
WO2011000546A1 (en) * | 2009-07-01 | 2011-01-06 | Bayer Materialscience Ag | Method for the production of a polyurethane polymer comprising polyester polyols that contain terminal secondary hydroxyl groups |
CN102471444B (en) * | 2009-07-01 | 2014-05-28 | 拜尔材料科学股份公司 | Process for preparing polyurethane polymers comprising polyester polyols having secondary hydroxyl end groups |
RU2543383C2 (en) * | 2009-07-01 | 2015-02-27 | Байер Матириальсайенс Аг | Method of obtaining polyurethane polymer, containing polyestherpolyols with terminal secondary hydroxyl groups |
US9139685B2 (en) | 2009-07-01 | 2015-09-22 | Bayer Materialscience Ag | Process for the preparation of a polyurethane polymer with secondary hydroxyl end groups comprising polyester polyols |
WO2013024108A1 (en) | 2011-08-16 | 2013-02-21 | Bayer Intellectual Property Gmbh | Method for producing a polyurethane/polyisocyanurate rigid foam |
WO2013024107A1 (en) | 2011-08-16 | 2013-02-21 | Bayer Intellectual Property Gmbh | Process for producing a rigid polyurethane-polyisocyanurate foam |
WO2015091471A1 (en) | 2013-12-18 | 2015-06-25 | Bayer Materialscience Ag | Method for working up alkaline polyether polyols |
US10131743B2 (en) | 2013-12-18 | 2018-11-20 | Covestro Deutschland Ag | Method for working up alkaline polyether polyols |
Also Published As
Publication number | Publication date |
---|---|
BE663892A (en) |
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