GB1390786A - Polyesteramides - Google Patents
PolyesteramidesInfo
- Publication number
- GB1390786A GB1390786A GB2306772A GB2306772A GB1390786A GB 1390786 A GB1390786 A GB 1390786A GB 2306772 A GB2306772 A GB 2306772A GB 2306772 A GB2306772 A GB 2306772A GB 1390786 A GB1390786 A GB 1390786A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- diamine
- polyesteramides
- fatty acids
- condensate
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
1390786 Polyesteramides VICTOR WOLF Ltd 3 July 1973 [17 May 1972] 23067/72 Headings C3R and C3P Polyesteramides are made by reacting substantially equivalent amounts of an acid component comprising a mixture of polymeric fatty acids, a monofuctional pre-condensate ester of formula in which R represents an alkyl or alkenyl radical, n is from 1-10 and * indicates the reactive site, with an alkylene diamine containing 2-4 C. The pre-condensate may be obtained by interaction of styrene and allyl alcohol followed by esterification of all save one of the -OH groups by reaction with C 10-24 saturated or unsaturated aliphatic acids, e.g. acetic, propionic, butyric, valeric, 2-ethyl hexanoic, isoctanoic, 2-methyl pentanoic, 2- ethyl butyric, isobutyric, 4-tert.-butyl benzoic, diphenolic, caprylic, caproic and benzoic acid. Additionally the reaction mixture may contain another diamine, e.g. an aliphatic, cycloaliphatic or aromatic diamine; another dicarboxylic acid; or an hydroxy acid. In examples tall oil fatty acids, stearic acid and ethylene diamine are preferred reactants. Organic or inorganic phosphites may be included as stabilizers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2306772A GB1390786A (en) | 1972-05-17 | 1972-05-17 | Polyesteramides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2306772A GB1390786A (en) | 1972-05-17 | 1972-05-17 | Polyesteramides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1390786A true GB1390786A (en) | 1975-04-16 |
Family
ID=10189587
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2306772A Expired GB1390786A (en) | 1972-05-17 | 1972-05-17 | Polyesteramides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1390786A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1696022A1 (en) * | 1996-10-18 | 2006-08-30 | Arizona Chemical Company | Ester-terminated polyamides gels |
-
1972
- 1972-05-17 GB GB2306772A patent/GB1390786A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1696022A1 (en) * | 1996-10-18 | 2006-08-30 | Arizona Chemical Company | Ester-terminated polyamides gels |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |