GB1000216A - Improvements in or relating to copolyamides - Google Patents
Improvements in or relating to copolyamidesInfo
- Publication number
- GB1000216A GB1000216A GB1290364A GB1290364A GB1000216A GB 1000216 A GB1000216 A GB 1000216A GB 1290364 A GB1290364 A GB 1290364A GB 1290364 A GB1290364 A GB 1290364A GB 1000216 A GB1000216 A GB 1000216A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbon atoms
- acids
- aliphatic
- hydrocarbon radical
- specified
- 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
- C08G69/34—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids using polymerised unsaturated fatty acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
Abstract
A process for the production of a copolyamide comprises condensing at a temperature of from 150 DEG to 300 DEG C., a polymerizable composition comprising (A) polymerized, saturated, ethylencally unsaturated or acetylenically unsaturated, naturally occurring or synthetic, monobasic, aliphatic acids containing from 8 to 24 carbon atoms, said polymerized acids having a dimeric fat acids content greater than about 95% by weight, (B) a compound selected from (a) R11OOC-COOR11, (b) R11-OOC-R1-COOR11 (c) the amide-forming derivatives of (a) and (b), (d) H2N-(CH2)xCOOR11 and (e) <FORM:1000216/C3/1> where R1 is an aliphatic hydrocarbon radical having from 1 to 20 carbon atoms, an alicyclic or aliphatic substituted alicyclic hydrocarbon radical having from 6 to 20 carbon atoms, or an aromatic or aliphatic substituted aromatic hydrocarbon aromatic hydrocarbon radical having from 6 to 20 carbon atoms, R11 is hydrogen or an alkyl group having from 1 to 8 carbon atoms and x is an integer of from 2 to 15, and (c) a diamine of the formula H2N-R-NH2, where R is an aliphatic hydrocarbon radical having from 4 to 20 carbon atoms, in which the molar equivalents of amine present are substantially equal to the molar equivalents of carboxyl group present. Specified monobasic, aliphatic acids are caprylic, pelargonic, capric, lauric, myristic, palmitic, isopalmitic, stearic, ararchidic behenic, lignocerice, 3-octenoic, 11-dodecenoic, linderic, lauroleic, myristoleic, tsuzuic, palmitoleic, gadoleic, cetoleic, nervonic, linoleic, oleic, linolenic, eleostearic, hiragonic, moroctic, timnodonic, eicosate traenoic, nisinic, scoliodonic, chaulmoogric, 10-undecynoic, tariric, stearolic, behenolic and isamic acid. Specified diamines are 1 : 6-diaminohexane, 1 : 4-diaminobutane, 1 : 10 - diaminodecane, 1 : 12-diaminonododecane, 1 : 18 - diaminooctadecane, 3 : 4 - diethyl - 1 : 6 - diaminohexane, 3 - ethyl - 1 : 8 - diaminooctane, 2 - nonyl-1 : 10 - diaminodecane and 2 - octyl - 1 : 11-diaminoundecane. Specified dicarboxylic acids are oxalic, malonic, adipic, pimelic, suberic, azelaic, sebacic, dodecanedoic, succinic, glutanic dimethyl malonic, dimethyl succinic, heptadecanedioic, tere- and iso-phthalic, naphthalene dicarboxylic and 1 : 4- and 1 : 3-cyclohexane dicarboxylic acid. Specified amino acids and lactams are aminocaproic acid, C-caprolactam, aminoundecanoic acid and co-capryllactam.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26857663A | 1963-03-28 | 1963-03-28 | |
BE645836A BE645836A (en) | 1963-03-28 | 1964-03-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1000216A true GB1000216A (en) | 1965-08-04 |
Family
ID=25655791
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1290364A Expired GB1000216A (en) | 1963-03-28 | 1964-03-26 | Improvements in or relating to copolyamides |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE645836A (en) |
DE (1) | DE1495967C3 (en) |
GB (1) | GB1000216A (en) |
NL (1) | NL152892B (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3499853A (en) * | 1964-05-23 | 1970-03-10 | Schering Ag | Polyamides |
US3717598A (en) * | 1968-12-05 | 1973-02-20 | Gen Mills Inc | Polyamide compositions |
US4045389A (en) * | 1975-07-31 | 1977-08-30 | Schering Aktiengesellschaft | Method of adhering textiles with a polyamide melt adhesive |
US4150002A (en) * | 1976-12-23 | 1979-04-17 | Schering Aktiengesellschaft | Polyamide melt adhesives |
US4212777A (en) * | 1977-10-28 | 1980-07-15 | Rhone-Poulenc Industries | Linear, flexible, high tensile strength copolyamides |
US4452974A (en) * | 1979-06-26 | 1984-06-05 | Rhone-Poulenc Industries | Preparation of hexamethylenediamine/adipic acid/dimer acid copolyamide |
US20100105812A1 (en) * | 2007-02-16 | 2010-04-29 | Arkema France | Copolyamide, composition containing such copolyamide and use thereof |
WO2012110413A1 (en) * | 2011-02-15 | 2012-08-23 | Dsm Ip Assets B.V. | Polyamide containing monomer units of 1,4-butylene diamine |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2534121C3 (en) * | 1975-07-31 | 1982-06-03 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Use of polyamides for bonding textiles |
DE3315529A1 (en) * | 1983-04-29 | 1984-11-08 | Plate Bonn Gmbh, 5300 Bonn | Use of copolyamides for the heat-sealing of textiles |
-
1964
- 1964-03-20 DE DE19641495967 patent/DE1495967C3/en not_active Expired
- 1964-03-26 NL NL6403333A patent/NL152892B/en not_active IP Right Cessation
- 1964-03-26 GB GB1290364A patent/GB1000216A/en not_active Expired
- 1964-03-27 BE BE645836A patent/BE645836A/xx unknown
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3499853A (en) * | 1964-05-23 | 1970-03-10 | Schering Ag | Polyamides |
US3717598A (en) * | 1968-12-05 | 1973-02-20 | Gen Mills Inc | Polyamide compositions |
US4045389A (en) * | 1975-07-31 | 1977-08-30 | Schering Aktiengesellschaft | Method of adhering textiles with a polyamide melt adhesive |
US4150002A (en) * | 1976-12-23 | 1979-04-17 | Schering Aktiengesellschaft | Polyamide melt adhesives |
US4212777A (en) * | 1977-10-28 | 1980-07-15 | Rhone-Poulenc Industries | Linear, flexible, high tensile strength copolyamides |
US4452974A (en) * | 1979-06-26 | 1984-06-05 | Rhone-Poulenc Industries | Preparation of hexamethylenediamine/adipic acid/dimer acid copolyamide |
US20100105812A1 (en) * | 2007-02-16 | 2010-04-29 | Arkema France | Copolyamide, composition containing such copolyamide and use thereof |
WO2012110413A1 (en) * | 2011-02-15 | 2012-08-23 | Dsm Ip Assets B.V. | Polyamide containing monomer units of 1,4-butylene diamine |
JP2014506614A (en) * | 2011-02-15 | 2014-03-17 | ディーエスエム アイピー アセッツ ビー.ブイ. | Polyamide containing monomer units of 1,4-butylenediamine |
Also Published As
Publication number | Publication date |
---|---|
NL6403333A (en) | 1964-09-29 |
BE645836A (en) | 1964-07-16 |
NL152892B (en) | 1977-04-15 |
DE1495967A1 (en) | 1969-07-03 |
DE1495967C3 (en) | 1975-03-27 |
DE1495967B2 (en) | 1974-07-25 |
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