GB1410005A - Polyamide - Google Patents
PolyamideInfo
- Publication number
- GB1410005A GB1410005A GB4296771A GB4296771A GB1410005A GB 1410005 A GB1410005 A GB 1410005A GB 4296771 A GB4296771 A GB 4296771A GB 4296771 A GB4296771 A GB 4296771A GB 1410005 A GB1410005 A GB 1410005A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diamine
- methyl
- residues
- acids
- per cent
- 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
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
- C08G69/265—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids from at least two different diamines or at least two different dicarboxylic acids
Abstract
1410005 Polyamides BP CHEMICALS INTERNATIONAL Ltd 15 Sept 1972 [15 Sept 1971] 42967/71 Heading C3R A polyamide contains acid residues, more than 80 mol. per cent of which are residues of an aromatic or alicyclic acid wherein n = 0 or 1 and the ring is unsubstituted or substituted by methyl, and amine residues which comprise residues of (I) between 10 and 80 moles per cent of optionally methyl-substituted m- or p-xylylene diamine and (II) over 20 and up to 90 moles per cent of an aliphatic diamine wherein q, s, t, u and w are integers totalling not more than 14 and R<SP>1</SP> to R<SP>4</SP> are each H or methyl with at least 2 on the same carbon atom being methyl. It may also contain up to 30 mol. per cent of (III) residues of a diamine wherein R 5 and R 6 are H or methyl and x+y+z #12. It is preferred that not more than 10 mol. per cent of residues of any other diamine is present. Specified acids are terephthalic, 1,4- phenylene diacetic and 1,4-cyclohexane dicarboxylic and diacetic acids as the essential acids, and adipic, suberic, sebacic, dodecane dioic, isophthalic, 1,2- or 1,3-cyclohexanol dicarboxylic or diacetic, and 1,2- or 1,3-phenylene diacetic acids as optional acids. Specified diamines are (II) 2,2,4- and 2,4,4-trimethyl hexamethylene diamine, 2,2,7,7-tetramethyl octamethylene diamine and 2,2-dimethyl pentamethylene diamine, and (III) hexa- and dodecamethylene, 5-methyl nonane 2-methyl pentamethylene, and 2- or 3-methyl or 2,5-dimethyl hexamethylene diamines. Up to 10 mol. per cent of residues of amino-acids or their lactams may also be present, e.g. capro- or lauro-lactam or #-amino hexanoic, undecanoic or dodecanoic acids. Conventional additives such as stabilizers, e.g. the stearyl ester of 3-(4-hydroxy-3,5-di-tbutylphenyl) propionic acid, triphenyl, diethyl hexyl or trisnonyl phosphite or ammonium hypophosphite, and plasticizers, e.g. N-butyl benzene sulphonamide, may be incorporated with the polymer during or after its preparation. In all the specific examples the acid is terephthalic, diamine (I) is a mixture of 70% meta, 30% para-xylylene diamines and (II) is a 50/50 mixture of 2,2,4- and 2,4,4-trimethyl hexamethylene diamines; some also include units of hexa- or dodeca-methylene diamine or caprolactam. It is stated that the selected combination of acid and amine residues in the specified proportions provides polyamides having a high impact strength, generally of at least 44 k JM<SP>-2</SP> while retaining good overall mechanical properties. Reference is made to Specifications 905,475; 1,176,985; 1,225,483 and 1,128,761.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4296771A GB1410005A (en) | 1971-09-15 | 1971-09-15 | Polyamide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4296771A GB1410005A (en) | 1971-09-15 | 1971-09-15 | Polyamide |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1410005A true GB1410005A (en) | 1975-10-15 |
Family
ID=10426757
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4296771A Expired GB1410005A (en) | 1971-09-15 | 1971-09-15 | Polyamide |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1410005A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0010520A1 (en) * | 1978-10-18 | 1980-04-30 | Ciba-Geigy Ag | Substituted derivatives of 11-amino-undeca-4,8 dienals and 11-amino undecanals and process for their preparation |
-
1971
- 1971-09-15 GB GB4296771A patent/GB1410005A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0010520A1 (en) * | 1978-10-18 | 1980-04-30 | Ciba-Geigy Ag | Substituted derivatives of 11-amino-undeca-4,8 dienals and 11-amino undecanals and process for their preparation |
US4355177A (en) | 1978-10-18 | 1982-10-19 | Ciba-Geigy Corporation | Substituted 11-amino-undeca-4,8-dienal and 11-amino-undecanal derivatives and processes for their preparation |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
CSNS | Application of which complete specification have been accepted and published, but patent is not sealed |