GB1410005A - Polyamide - Google Patents

Polyamide

Info

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
Application number
GB4296771A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BP Chemicals Ltd
Original Assignee
BP Chemicals Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by BP Chemicals Ltd filed Critical BP Chemicals Ltd
Priority to GB4296771A priority Critical patent/GB1410005A/en
Publication of GB1410005A publication Critical patent/GB1410005A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/26Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
    • C08G69/265Polyamides 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.
GB4296771A 1971-09-15 1971-09-15 Polyamide Expired GB1410005A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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