GB891579A - Improvements in the production of expandable polyamides - Google Patents
Improvements in the production of expandable polyamidesInfo
- Publication number
- GB891579A GB891579A GB23742/60A GB2374260A GB891579A GB 891579 A GB891579 A GB 891579A GB 23742/60 A GB23742/60 A GB 23742/60A GB 2374260 A GB2374260 A GB 2374260A GB 891579 A GB891579 A GB 891579A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- diformate
- esters
- diamines
- polyamide
- 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
- C08J2377/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C08J2377/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
Abstract
Expandable polyamide compositions are prepared by heating polyamide-forming substances in the presence of (1) esters of carboxylic acids with 1-3 carbon atoms and polyhydric alcohols and (2) N-hydroxyalkyl diamines or their salts with dicarboxylic acids at temperatures at which condensation but no foam formation takes place, e.g. 180 DEG -240 DEG C., until the polyamide formed is still at least partly soluble in sulphuric acid. Specified reaction mixture components are:- polyamide-forming substances dicarboxylic acid salts of diamines, e.g. adipic acid hexamethylene diamine, sebacic acid hexamethylene diamine and suberic acid octamethylene diamine; omega-aminocarboxylic acids, e.g. omega-aminocaproic acid; and lactams, e.g. caprolactam, oenanthic lactam and caprylic lactam: esters ethylene glycol diformate, ethylene glycol oxalate, propylene glycol diformate, glycerine diformate and triformate, trimethylol-propane diformate and triformate, pentaerythritol formate, trimethylol cyclohexanol formate and diethanolamine diformate: N-hydroxyalkyl diamines the reaction products of alkylene oxides or aldehydes with aliphatic, cycloaliphatic or aromatic diamines or the dicarboxylic acid salts of these products, e.g. N-hydroxyethyl-hexamethylene diamine or its adipate. The reaction mixture may also include the carboxylic acid esters specified in the parent Specification or oxamic acid or esters as specified in Specification 858,254. The compositions are converted into powder form and expanded by further heating at 275 DEG -280 DEG C. by the decomposition of the ester.ALSO:Expandable polyamide compositions are prepared by heating polyamide-forming substances in the presence of (1) esters of carboxylic acids with 1-3 carbon atoms and polyhydric alcohols and (2)N-hydroxyalkyl-diamines or their salts with dicarboxylic acids at temperatures at which condensation but no foam formation takes place, e.g. 180-240 DEG C., until the polyamide formed is still at least partly soluble in sulphuric acid. Specified reaction mixture components are: polyamide-forming substances dicarboxylic acid salts of diamines e.g. adipic acid hexamethylene diamine, sebacic acid hexamethylene diamine and suberic acid octamethylene diamine; omega-aminocarboxylic acids e.g. omega-amino caproic acid; and lactams e.g. caprolactam, oenanthic lactam and caprylic lactam: esters ethylene glycol diformate, ethylene glycol oxalate, propylene glycol diformate, glycerine diformate, glycerine triformate, trimethylol-propane diformate, trimethylol-propane triformate, pentalrythritol formate, trimethylol cyclohexanol formate and diethanolamine diformate: N-hydroxyalkyl diamines the reaction products of alkylene oxides or aldehydes with aliphatic, cycloaliphatic or aromatic diamines or the dicarboxylic acid salts af these products, e.g. N-hydroxyethyl-hexamethylene diamine or its adipate. The reaction mixture may also include the carboxylic acid esters specified in the parent Specification or oxamic acid or esters as specified in Specification 858,254. The compositions are converted into powder form and expanded by further heating at 275-280 DEG C. by the decomposition of the ester.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE891579X | 1959-07-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB891579A true GB891579A (en) | 1962-03-14 |
Family
ID=6845971
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23742/60A Expired GB891579A (en) | 1959-07-10 | 1960-07-07 | Improvements in the production of expandable polyamides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB891579A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2080910A2 (en) * | 1970-01-16 | 1971-11-26 | Ici Ltd | |
WO2011007043A1 (en) * | 2009-07-14 | 2011-01-20 | Kemira Oyj | Biocidal composition for wood, method for wood treatment, and wood produced thereby |
-
1960
- 1960-07-07 GB GB23742/60A patent/GB891579A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2080910A2 (en) * | 1970-01-16 | 1971-11-26 | Ici Ltd | |
WO2011007043A1 (en) * | 2009-07-14 | 2011-01-20 | Kemira Oyj | Biocidal composition for wood, method for wood treatment, and wood produced thereby |
US9125404B2 (en) | 2009-07-14 | 2015-09-08 | Tmainco Finland | Biocidal composition for wood, method for wood treatment, and wood produced thereby |
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