DE1570645A1 - Polyamid-Kunstharze - Google Patents
Polyamid-KunstharzeInfo
- Publication number
- DE1570645A1 DE1570645A1 DE19651570645 DE1570645A DE1570645A1 DE 1570645 A1 DE1570645 A1 DE 1570645A1 DE 19651570645 DE19651570645 DE 19651570645 DE 1570645 A DE1570645 A DE 1570645A DE 1570645 A1 DE1570645 A1 DE 1570645A1
- Authority
- DE
- Germany
- Prior art keywords
- acid
- fatty acids
- acids
- polymeric
- dimeric
- 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.)
- Pending
Links
- 239000004952 Polyamide Substances 0.000 title claims description 14
- 229920002647 polyamide Polymers 0.000 title claims description 14
- 229920003002 synthetic resin Polymers 0.000 title description 4
- 239000000057 synthetic resin Substances 0.000 title description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 38
- 229930195729 fatty acid Natural products 0.000 claims description 38
- 239000000194 fatty acid Substances 0.000 claims description 38
- 150000004665 fatty acids Chemical class 0.000 claims description 38
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 210000003608 fece Anatomy 0.000 claims 1
- 239000002253 acid Substances 0.000 description 23
- 150000007513 acids Chemical class 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 239000000178 monomer Substances 0.000 description 8
- 239000000539 dimer Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- 239000013638 trimer Substances 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 3
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- KYXHKHDZJSDWEF-LHLOQNFPSA-N CCCCCCC1=C(CCCCCC)C(\C=C\CCCCCCCC(O)=O)C(CCCCCCCC(O)=O)CC1 Chemical compound CCCCCCC1=C(CCCCCC)C(\C=C\CCCCCCCC(O)=O)C(CCCCCCCC(O)=O)CC1 KYXHKHDZJSDWEF-LHLOQNFPSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- RGTIBVZDHOMOKC-UHFFFAOYSA-N stearolic acid Chemical compound CCCCCCCCC#CCCCCCCCC(O)=O RGTIBVZDHOMOKC-UHFFFAOYSA-N 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- GCORITRBZMICMI-CMDGGOBGSA-N (e)-dodec-4-enoic acid Chemical compound CCCCCCC\C=C\CCC(O)=O GCORITRBZMICMI-CMDGGOBGSA-N 0.000 description 1
- ZONJATNKKGGVSU-UHFFFAOYSA-N 14-methylpentadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCC(O)=O ZONJATNKKGGVSU-UHFFFAOYSA-N 0.000 description 1
- NNERWURVSCBMJE-UHFFFAOYSA-N 2-oxospiro[1h-indole-3,2'-1h-quinazoline]-4'-carboxylic acid Chemical compound O=C1NC2=CC=CC=C2C11N=C(C(=O)O)C2=CC=CC=C2N1 NNERWURVSCBMJE-UHFFFAOYSA-N 0.000 description 1
- -1 3-octenonic acid Chemical class 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 235000021353 Lignoceric acid Nutrition 0.000 description 1
- CQXMAMUUWHYSIY-UHFFFAOYSA-N Lignoceric acid Natural products CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCC1=CC=C(O)C=C1 CQXMAMUUWHYSIY-UHFFFAOYSA-N 0.000 description 1
- GCORITRBZMICMI-UHFFFAOYSA-N Linderic acid Natural products CCCCCCCC=CCCC(O)=O GCORITRBZMICMI-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000005643 Pelargonic acid Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 241000282898 Sus scrofa Species 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- VUXNZDYAHSFXBM-UHFFFAOYSA-N docos-13-ynoic acid Chemical compound CCCCCCCCC#CCCCCCCCCCCCC(O)=O VUXNZDYAHSFXBM-UHFFFAOYSA-N 0.000 description 1
- FARYTWBWLZAXNK-WAYWQWQTSA-N ethyl (z)-3-(methylamino)but-2-enoate Chemical compound CCOC(=O)\C=C(\C)NC FARYTWBWLZAXNK-WAYWQWQTSA-N 0.000 description 1
- 150000003948 formamides Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US341693A US3396180A (en) | 1964-01-31 | 1964-01-31 | Polyamide resin compositions of ethylene-diamine and fractionated polymeric fat acids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1570645A1 true DE1570645A1 (de) | 1970-07-09 |
Family
ID=23338631
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19651570645 Pending DE1570645A1 (de) | 1964-01-31 | 1965-01-15 | Polyamid-Kunstharze |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3396180A (en, 2012) |
| BE (1) | BE659059A (en, 2012) |
| CH (1) | CH432838A (en, 2012) |
| DE (1) | DE1570645A1 (en, 2012) |
| FR (1) | FR1421153A (en, 2012) |
| GB (1) | GB1044861A (en, 2012) |
| NL (1) | NL6501120A (en, 2012) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4032549A (en) * | 1976-03-29 | 1977-06-28 | Emery Industries, Inc. | Reactive liquid polyamides from amine residues |
| US4207217A (en) * | 1976-12-20 | 1980-06-10 | Chem-Plast S.P.A. | Heat melting adhesive |
| US4184099A (en) * | 1977-04-27 | 1980-01-15 | International Flavors & Fragrances Inc. | Composition for slow release of volatile ingredients at _high temperature; and article comprising same |
| IT1180214B (it) * | 1984-08-02 | 1987-09-23 | Chem Plast Spa | Promotori d'adesione per plastisols in grado di mantenere stabile il colore dei plastisols all'effetto del trattamento termico d'applicazione |
| US20030086815A1 (en) * | 2001-11-07 | 2003-05-08 | Wesley John N | Fragrance throwing liquid candle |
| EP2892966A4 (en) | 2011-09-06 | 2016-06-15 | Flint Trading Inc | Antifoaming agents for hot-melt adhesives |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2450940A (en) * | 1944-04-20 | 1948-10-12 | John C Cowan | Polyamides from polymeric fat acids |
| US2495008A (en) * | 1947-01-18 | 1950-01-17 | American Marietta Co | Adhesive tape |
| US2635974A (en) * | 1949-11-15 | 1953-04-21 | Us Playing Card Co | Decorating strip with heat activated adhesive |
| US2550682A (en) * | 1950-04-28 | 1951-05-01 | Falkenburg Lee Bert | Coating compositiions |
-
1964
- 1964-01-31 US US341693A patent/US3396180A/en not_active Expired - Lifetime
-
1965
- 1965-01-15 DE DE19651570645 patent/DE1570645A1/de active Pending
- 1965-01-15 GB GB1958/65A patent/GB1044861A/en not_active Expired
- 1965-01-20 FR FR2605A patent/FR1421153A/fr not_active Expired
- 1965-01-28 NL NL6501120A patent/NL6501120A/xx unknown
- 1965-01-29 CH CH125365A patent/CH432838A/fr unknown
- 1965-01-29 BE BE659059A patent/BE659059A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE659059A (en, 2012) | 1965-05-17 |
| GB1044861A (en) | 1966-10-05 |
| CH432838A (fr) | 1967-03-31 |
| FR1421153A (fr) | 1965-12-10 |
| US3396180A (en) | 1968-08-06 |
| NL6501120A (en, 2012) | 1965-08-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69216500T2 (de) | Härtbare Harzzusammensetzungen und Verfahren zur Herstellung | |
| DE1645414C3 (de) | Verfahren zur Herstellung von Copolyamiden und deren Verwendung als Schmelzkleber | |
| EP0023956B1 (de) | Verfahren zur Herstellung von Polyether(ester)amiden | |
| DE1720819A1 (de) | Verfahren zum Herstellen eines Kunststoff-Klebstoffes auf der Grundlage von Polyamiden | |
| DE1595764A1 (de) | Verfahren zum Herstellen von Polyamid-Kunststoffen | |
| DE1570645A1 (de) | Polyamid-Kunstharze | |
| DE2152194B2 (de) | Verfahren zur Herstellung von Polylaurinlactam | |
| DE2148264A1 (de) | Neue polyamide, deren herstellung und verwendung | |
| DE1745917A1 (de) | Polyamidkunstharz | |
| DE1720832A1 (de) | Verfahren zum Herstellen von Polyamiden | |
| EP0325740B1 (de) | In der Kälte schlagzähe thermoplastische Formmassen | |
| DE1940622A1 (de) | Massen aus anionisch polymerisiertem Polycaprolactam und Poly | |
| DE1719192B2 (de) | Klebfolien aus Polyamiden und/oder Polyesteramiden | |
| DE1914561A1 (de) | Thermoplastische Zusammensetzungen auf der Basis von Polyolefinen und Polyamiden | |
| DE1594022C3 (de) | Klebstoff auf Basis von wäßrigen Polyamidharz-Dispersionen | |
| DE1165861B (de) | Verfahren zur Herstellung N-alkylierter Polymethacrylsaeureimide | |
| EP0093085A2 (de) | Verfahren zur Herstellung eines lagerfähigen, mischbaren Härters für Acrylatklebharze | |
| DE1495925A1 (de) | Nicht sproede Kunstharze aus fraktionierten polymeren Fettsaeuren | |
| DE1520002A1 (de) | Verfahren zum Herstellen von copolymeren Polyesteramid-Polyamidgemischen,die als Bindemittel fuer Dichtungsnaehte von Metallbehaeltern geeignet sind | |
| EP0381973B1 (de) | Verfahren zur Herstellung von Nitrilgruppen enthaltenden Copolymerisaten auf Basis von Ethylen | |
| DE1196373B (de) | Verfahren zur Herstellung von Formkoerpern, UEberzuegen oder Verklebungen | |
| DE1102322B (de) | Verfahren zur Herstellung einer thermoplastischen Klebmasse | |
| DE1595747A1 (de) | Verfahren zum Herstellen von Polyamidkunststoffen hoher Zerreissfestigkeit und geringer Wasserabsorption | |
| DE903863C (de) | Verfahren zur Herstellung von Polyadditionsprodukten | |
| DE2142307A1 (de) | Kalt- oder warmhaertende loesungsmittelfreie fluessige ueberzugsmittel, dichtmassen, kleb- oder kunststoffe |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| SH | Request for examination between 03.10.1968 and 22.04.1971 |