GB1410007A - Polyamide - Google Patents

Polyamide

Info

Publication number
GB1410007A
GB1410007A GB4296971A GB4296971A GB1410007A GB 1410007 A GB1410007 A GB 1410007A GB 4296971 A GB4296971 A GB 4296971A GB 4296971 A GB4296971 A GB 4296971A GB 1410007 A GB1410007 A GB 1410007A
Authority
GB
United Kingdom
Prior art keywords
residues
diamine
mol
per cent
acid
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
GB4296971A
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 GB4296971A priority Critical patent/GB1410007A/en
Publication of GB1410007A publication Critical patent/GB1410007A/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

1410007 Polyamides BP CHEMICALS INTERNATIONAL Ltd 15- Sept 1972 [15 Sept 1971] 42969/71 Heading C3R A polyamide comprises (a) residues of an aromatic or alicyclic diacid where n is 0 or 1 and the ring is unsubstituted or substituted by methyl, and (b) diamine residues comprising (I) 10 to 40 mol. per cent of residues of isophorone diamine, (II) over 20 and up to 80 mol. per cent of residues of a diamine where q to w total not more than 20 and R<SP>1</SP> to R<SP>4</SP> are each H or methyl at least 2 thereof attached to the same carbon atom being methyl, and (III) 10 to 50 mol. per cent of residues of a diamine where 4#x+y+z#12 and R<SP>5</SP> and R<SP>6</SP> are H or methyl, the specified acid residues (a) constituting at least 80 mol. per cent of the total diacid residues and the specified residues (b) constituting at least 90 mol. per cent of the total diamine residues. The selected range of proportions of the specified residues and restriction on unspecified residues is stated to result in polymers of high impact strength while retaining good overall mechanical properties. Any balance of acid residue may be those of adipic, suberic, sebacic or dodecanoic acid or a 1,2- or 1,3-isomer of the acids (a). Up to 15 mol. per cent of residue of amino acids or lactams may also be included, e.g. capro- or dodecano-lactam or 6-amino caproic or 11-amino undecanoic acid. Conventional additives such as stabilizers, e.g. trihydrocarbyl phosphites, ammonium hypophosphite or the stearyl ester of 3-(4-hydroxy- 3,5 - di - t - butyl phenyl) propionic acid, and plasticizers, e.g. N-butyl benzene sulphonamide, may be incorporated with the polymer during or after its preparation. In the specific examples residues (a) are those of terephthalic acid; (b) (II) of trimethyl hexamethylene diamine; and (b) (III) of dodeca- or hexa-methylene diamine. Example 6 also includes 10% of caprolactam residues. Reference is made to Specifications 905,475; 1,096,908; 1,100,972; 1,132,039; 1,176,985; 1,228,761; 1,255,483; and 1,266,864.
GB4296971A 1971-09-15 1971-09-15 Polyamide Expired GB1410007A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4296971A GB1410007A (en) 1971-09-15 1971-09-15 Polyamide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4296971A GB1410007A (en) 1971-09-15 1971-09-15 Polyamide

Publications (1)

Publication Number Publication Date
GB1410007A true GB1410007A (en) 1975-10-15

Family

ID=10426767

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4296971A Expired GB1410007A (en) 1971-09-15 1971-09-15 Polyamide

Country Status (1)

Country Link
GB (1) GB1410007A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0010522A1 (en) * 1978-10-18 1980-04-30 Ciba-Geigy Ag Transparent copolyamides, process for their production and their use in the manufacture of moulded articles
EP0010521A1 (en) * 1978-10-18 1980-04-30 Ciba-Geigy Ag Transparent copolyamide and its use in the manufacture of moulded articles
EP0042820A2 (en) * 1980-06-23 1981-12-30 Ciba-Geigy Ag Transparent copolyamides and their use in producing shaped articles
US4345066A (en) 1979-09-12 1982-08-17 Chemische Werke Huls Ag Transparent copolyamides and their application to transparent, impact resistant molded articles

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0010522A1 (en) * 1978-10-18 1980-04-30 Ciba-Geigy Ag Transparent copolyamides, process for their production and their use in the manufacture of moulded articles
EP0010521A1 (en) * 1978-10-18 1980-04-30 Ciba-Geigy Ag Transparent copolyamide and its use in the manufacture of moulded articles
US4345066A (en) 1979-09-12 1982-08-17 Chemische Werke Huls Ag Transparent copolyamides and their application to transparent, impact resistant molded articles
EP0042820A2 (en) * 1980-06-23 1981-12-30 Ciba-Geigy Ag Transparent copolyamides and their use in producing shaped articles
EP0042820A3 (en) * 1980-06-23 1982-08-25 Ciba-Geigy Ag Transparent copolyamides and their use in producing shaped articles
US4377683A (en) 1980-06-23 1983-03-22 Ciba-Geigy Corporation Transparent copolyamide from isophorone diamine and substituted undecane diamine

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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