GB934629A - Foamed materials - Google Patents
Foamed materialsInfo
- Publication number
- GB934629A GB934629A GB37816/59A GB3781659A GB934629A GB 934629 A GB934629 A GB 934629A GB 37816/59 A GB37816/59 A GB 37816/59A GB 3781659 A GB3781659 A GB 3781659A GB 934629 A GB934629 A GB 934629A
- Authority
- GB
- United Kingdom
- Prior art keywords
- novolak
- phenol
- resorcinol
- moles
- formaldehyde
- 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
- C08G18/54—Polycondensates of aldehydes
- C08G18/546—Oxyalkylated polycondensates of aldehydes
-
- 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
-
- 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
- C08G2110/0058—≥50 and <150kg/m3
-
- 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
- C08G2110/0083—Foam properties prepared using water as the sole blowing agent
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
A process for the production of a rigid polyurethane foam comprises reacting an alkoxylated novolak resin with a polyisocyanate and water in the presence of a polyurethane-forming catalyst. By an alkoxylated novolak resin is meant a novolak resin in which at least one phenolic group per molecule has been etherified by reaction with an a ,b -alkylene oxide. The novolak can be derived from such phenols as phenol itself, cresols, difunctional xylenols, resorcinol and diphenylol propane, and from formaldehyde, acetaldehyde and benzaldehyde. 1,2-Ethylene-, propylene- and butylene oxides are specified alkylene oxides. They may be reacted with the novolak or with the phenol before reaction with the aldehyde is effected. Catalysts for the foam formation include triethylamine and triethylene diamine. In examples (1) an ethoxylated novolak is prepared by reacting (with a hydrochloric acid catalyst) formaldehyde and an ethoxylated phenol (from phenol and 5,2 moles of ethylene oxide). Ethyl cellulose and wetting agent are then dissolved in heated novolak and, after cooling, foaming is effected by adding zinc naphthenate in white spirit, aqueous triethylene diamine and a commercial tolylene diisocyanate mixture. Sufficient heat is generated to cure the foam. (6) A similar process is carried out using a novolak obtained from an addition product of 7,7 moles of ethylene oxide with 1 mole of resorcinol. Specifications 758,249, 775,459, 909,777 and 909,842 are referred to.ALSO:A process for the production of a rigid polyurethane foam comprises reacting an alkoxylated novolak resin with a polyisocyanate and water in the presence of a polyurethaneforming catalyst. By an alkoxylated novolak resin is meant a novolak resin in which at least one phenolic group per molecule has been etherified by reaction with an a , b -alkylene oxide. The novolak can be derived form such phenols as phenol itself, cresols, difunctional xylenols, resorcinol and diphenylol propane, and from formaldehyde, acetaldehyde and benzaldehyde. 1, 2-Ethylene-, propylene- and butylene oxides are specified alkylene oxides. They may be reacted with the novolak or with the phenol before reaction with the aldehyde is effected. Catalysts for the foam formation include triethylamine and triethylene diamine. In examples (1) an ethoxylated novolak is prepared by reacting (with a hydrochloric acid catalyst) formaldehyde and an ethoxylated phenol (from phenol and 5,2 moles of ethylene oxide). Ethyl cellulose and wetting agent are then dissolved in the heated novolak and after cooling, foaming is effected by adding zinc naphthenate, white spirit, aqueous triethylene diamine and a commercial tolylene diisocyanate mixture. Sufficient heat is generated to cure the foam; (6) a similar process is carried out using a novolak obtained from an addition product of 7,7 moles of ethylene oxide with 1 mole of resorcinol. Specifications 758,249, 775,459, 909,777 and 909,842 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB37816/59A GB934629A (en) | 1959-11-07 | 1959-11-07 | Foamed materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB37816/59A GB934629A (en) | 1959-11-07 | 1959-11-07 | Foamed materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB934629A true GB934629A (en) | 1963-08-21 |
Family
ID=10399203
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB37816/59A Expired GB934629A (en) | 1959-11-07 | 1959-11-07 | Foamed materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB934629A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2359865A1 (en) * | 1976-07-30 | 1978-02-24 | Texaco Development Corp | UETHANE POLYISOCYANURATE RIGID FOAM |
EP0397378A1 (en) * | 1989-05-06 | 1990-11-14 | MITSUI TOATSU CHEMICALS, Inc. | Hydrochlorofluorocarbon blown rigid polyurethane foams and their preparation |
EP0483431A1 (en) * | 1990-11-02 | 1992-05-06 | MITSUI TOATSU CHEMICALS, Inc. | Polyol and utilization thereof |
US5198475A (en) * | 1990-10-31 | 1993-03-30 | Mitsui Toatsu Chemicals, Inc. | Polyol and utilization thereof |
US10435503B2 (en) | 2017-09-22 | 2019-10-08 | Hexion Inc. | Compositions for polyurethane applications |
US10604614B2 (en) | 2017-09-22 | 2020-03-31 | Hexion Inc. | Compositions and methods to produce alkoxylated triazine-arylhydroxy-aldehyde condensates |
US10640475B2 (en) | 2017-09-22 | 2020-05-05 | Hexion Inc. | Compositions and methods to produce alkoxylated triazine-arlhydroxy-aldehyde condensates |
EP3819332A1 (en) * | 2019-11-06 | 2021-05-12 | Basf Se | Process for producing rigid polyurethane foams |
CN117965143A (en) * | 2024-04-02 | 2024-05-03 | 中国石油大学(华东) | Compression-resistant composite resin plugging agent and preparation method and application thereof |
-
1959
- 1959-11-07 GB GB37816/59A patent/GB934629A/en not_active Expired
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2359865A1 (en) * | 1976-07-30 | 1978-02-24 | Texaco Development Corp | UETHANE POLYISOCYANURATE RIGID FOAM |
EP0397378A1 (en) * | 1989-05-06 | 1990-11-14 | MITSUI TOATSU CHEMICALS, Inc. | Hydrochlorofluorocarbon blown rigid polyurethane foams and their preparation |
US5107068A (en) * | 1989-05-06 | 1992-04-21 | Mitsui Toatsu Chemicals, Inc. | Polyurethane resin and utilization thereof |
US5198475A (en) * | 1990-10-31 | 1993-03-30 | Mitsui Toatsu Chemicals, Inc. | Polyol and utilization thereof |
EP0483431A1 (en) * | 1990-11-02 | 1992-05-06 | MITSUI TOATSU CHEMICALS, Inc. | Polyol and utilization thereof |
US10435503B2 (en) | 2017-09-22 | 2019-10-08 | Hexion Inc. | Compositions for polyurethane applications |
US10604614B2 (en) | 2017-09-22 | 2020-03-31 | Hexion Inc. | Compositions and methods to produce alkoxylated triazine-arylhydroxy-aldehyde condensates |
US10640475B2 (en) | 2017-09-22 | 2020-05-05 | Hexion Inc. | Compositions and methods to produce alkoxylated triazine-arlhydroxy-aldehyde condensates |
US11028219B2 (en) | 2017-09-22 | 2021-06-08 | Hexion Inc. | Compositions for polyurethane applications |
EP3819332A1 (en) * | 2019-11-06 | 2021-05-12 | Basf Se | Process for producing rigid polyurethane foams |
CN117965143A (en) * | 2024-04-02 | 2024-05-03 | 中国石油大学(华东) | Compression-resistant composite resin plugging agent and preparation method and application thereof |
CN117965143B (en) * | 2024-04-02 | 2024-06-07 | 中国石油大学(华东) | Compression-resistant composite resin plugging agent and preparation method and application thereof |
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