GB723467A - Improved cellular phenolic resin - Google Patents
Improved cellular phenolic resinInfo
- Publication number
- GB723467A GB723467A GB20301/52A GB2030152A GB723467A GB 723467 A GB723467 A GB 723467A GB 20301/52 A GB20301/52 A GB 20301/52A GB 2030152 A GB2030152 A GB 2030152A GB 723467 A GB723467 A GB 723467A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ether
- acid
- phenol
- specified
- methyl
- 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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/142—Compounds containing oxygen but no halogen atom
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2361/00—Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
- C08J2361/04—Condensation polymers of aldehydes or ketones with phenols only
- C08J2361/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Low density resin foams of uniform texture are made by adding an aliphatic ether, having a boiling point not in excess of 150 DEG C., in an amount of 0.5 to 10 per cent by weight of the resin and an acid selected from hydrochloric, sulphuric, nitric, and water-soluble aromatic sulphonic acids, to a heat-hardenable liquid A-stage monohydric phenol-formaldehyde condensate containing less than 10 per cent by weight of water. The ether may be mixed with the condensate before the acid is added, or preferably the acid and ether are mixed together and then added to the condensate. Ageing of the acid-ether mixture at room temperature for 24 to 28 hours results in a firm uniform foamed structure. Phosphoric acid may be added in an amount equal to the specified acids which are used in amounts of 1 to 2 per cent by weight of the neutral mixture of the resin and ether. Ethers specified are dimethyl, diethyl, diisopropyl, n-butyl, methyl-tertiary butyl, isopropyl-tertiary butyl, methyl-isopropyl and methyl-ethyl ethers. The liquid condensates specified are the alkaline catalysed reaction products of 1.3 to 1.6 mols. of formaldehyde with 1 mol. of a monohydric phenol, e.g. phenol, m-cresol, m-xylenol or a mixture of phenol and o-cresol. Catalysts specified are sodium, potassium, barium and ammonium hydroxides, magnesium oxide, diethylamine and ethylene diamine. In examples, liquid condensates made from phenol and formalin in the presence of (1) barium hydroxide, and (2) caustic soda, are foamed by rapidly mixing with polyethylene ether of sorbitan monopalmitate, hydrochloric acid, sodium bicarbonate and diethyl ether. Other foams are made by using other ethers, a different acid, other esters or by omitting the bicarbonate. U.S.A. Specification 2,446,429 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US723467XA | 1951-09-10 | 1951-09-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB723467A true GB723467A (en) | 1955-02-09 |
Family
ID=22107009
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB20301/52A Expired GB723467A (en) | 1951-09-10 | 1952-08-12 | Improved cellular phenolic resin |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE518129A (en) |
CH (1) | CH309193A (en) |
GB (1) | GB723467A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4216295A (en) * | 1976-12-20 | 1980-08-05 | Monsanto Company | Foamable resole resin composition |
US4882364A (en) * | 1987-08-28 | 1989-11-21 | Fiberglas Canada Inc. | Process for manufacturing closed cell phenolic foams |
-
0
- BE BE518129D patent/BE518129A/xx unknown
-
1952
- 1952-08-12 GB GB20301/52A patent/GB723467A/en not_active Expired
-
1953
- 1953-03-05 CH CH309193D patent/CH309193A/en unknown
Also Published As
Publication number | Publication date |
---|---|
CH309193A (en) | 1955-08-31 |
BE518129A (en) |
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