CA1076742A - Copolyamides - Google Patents
CopolyamidesInfo
- Publication number
- CA1076742A CA1076742A CA245,730A CA245730A CA1076742A CA 1076742 A CA1076742 A CA 1076742A CA 245730 A CA245730 A CA 245730A CA 1076742 A CA1076742 A CA 1076742A
- Authority
- CA
- Canada
- Prior art keywords
- acid
- carbon atoms
- salt
- weight
- copolyamides
- 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
- 150000003839 salts Chemical class 0.000 claims abstract description 11
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 12
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 10
- 150000004885 piperazines Chemical class 0.000 claims description 10
- WMRCTEPOPAZMMN-UHFFFAOYSA-N 2-undecylpropanedioic acid Chemical compound CCCCCCCCCCCC(C(O)=O)C(O)=O WMRCTEPOPAZMMN-UHFFFAOYSA-N 0.000 claims description 6
- 235000011037 adipic acid Nutrition 0.000 claims description 5
- 239000001361 adipic acid Substances 0.000 claims description 5
- MRNZSTMRDWRNNR-UHFFFAOYSA-N bis(hexamethylene)triamine Chemical class NCCCCCCNCCCCCCN MRNZSTMRDWRNNR-UHFFFAOYSA-N 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract description 16
- -1 cyclic lactam Chemical class 0.000 abstract description 7
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract description 6
- 125000001931 aliphatic group Chemical group 0.000 abstract description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 abstract description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract description 2
- 239000012943 hotmelt Substances 0.000 abstract description 2
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract description 2
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 11
- 239000000306 component Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 3
- 238000004026 adhesive bonding Methods 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- JZLWSRCQCPAUDP-UHFFFAOYSA-N 1,3,5-triazine-2,4,6-triamine;urea Chemical compound NC(N)=O.NC1=NC(N)=NC(N)=N1 JZLWSRCQCPAUDP-UHFFFAOYSA-N 0.000 description 1
- YOOSAIJKYCBPFW-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)butoxy]propan-1-amine Chemical compound NCCCOCCCCOCCCN YOOSAIJKYCBPFW-UHFFFAOYSA-N 0.000 description 1
- OXEZLYIDQPBCBB-UHFFFAOYSA-N 4-(3-piperidin-4-ylpropyl)piperidine Chemical compound C1CNCCC1CCCC1CCNCC1 OXEZLYIDQPBCBB-UHFFFAOYSA-N 0.000 description 1
- 241000905957 Channa melasoma Species 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- HOQIYICTIBDBQU-UHFFFAOYSA-N [4-[2-[4-(aminomethyl)cyclohexyl]propan-2-yl]cyclohexyl]methanamine Chemical compound NCC1CCC(CC1)C(C)(C)C1CCC(CC1)CN HOQIYICTIBDBQU-UHFFFAOYSA-N 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical compound CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- YDLSUFFXJYEVHW-UHFFFAOYSA-N azonan-2-one Chemical compound O=C1CCCCCCCN1 YDLSUFFXJYEVHW-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08G69/36—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino acids, polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (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 |
|---|---|---|---|
| DE19752509791 DE2509791A1 (de) | 1975-03-06 | 1975-03-06 | Copolyamide und deren verwendung als schmelzkleber |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1076742A true CA1076742A (en) | 1980-04-29 |
Family
ID=5940641
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA245,730A Expired CA1076742A (en) | 1975-03-06 | 1976-02-13 | Copolyamides |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4102871A (enExample) |
| JP (1) | JPS51111897A (enExample) |
| BE (1) | BE839098A (enExample) |
| CA (1) | CA1076742A (enExample) |
| CH (1) | CH621136A5 (enExample) |
| DE (1) | DE2509791A1 (enExample) |
| FR (1) | FR2303039A1 (enExample) |
| GB (1) | GB1539600A (enExample) |
| SE (1) | SE7602158L (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2924323C2 (de) * | 1979-06-15 | 1988-10-20 | Chemische Werke Hüls AG, 4370 Marl | Kraftstoffbeständige Schmelzkleber |
| US4423204A (en) * | 1982-09-02 | 1983-12-27 | The Upjohn Company | Amorphous copolyamide from lactam, dicarboxylic acid and bisimidazoline |
| DE3531941A1 (de) * | 1985-09-07 | 1987-03-12 | Henkel Kgaa | Polyamidharze |
| CH674518A5 (enExample) * | 1987-09-09 | 1990-06-15 | Inventa Ag | |
| DE3730504C1 (en) * | 1987-09-11 | 1989-03-16 | Atochem Werke Gmbh | Copolyamides containing caprolactam and laurolactam, process for the preparation thereof and use thereof for heat-sealing textiles |
| CH682617B5 (de) * | 1989-02-20 | 1994-04-29 | Atochem Werke Gmbh | Copolyamide auf Basis von Caprolactam und Laurinlactam, Verfahren zu deren Herstellung und Verwendung derselben zum Heisssiegeln von Textilien. |
| DE4111670A1 (de) * | 1991-04-10 | 1992-10-15 | Schering Ag | Polyamidharze und deren verwendung fuer den reliefdruck |
| EP0536681A1 (de) * | 1991-10-11 | 1993-04-14 | Ems-Inventa Ag | Sperrschicht aus Copolyamid, ihre Verwendung sowie diese Sperrschicht enthaltende Mehrweg-Mehrschicht-Verpackungskörper |
| CH684747A5 (de) * | 1991-10-31 | 1994-12-15 | Inventa Ag | Mehrschicht-Verbund. |
| DE19512004C2 (de) * | 1995-03-31 | 1997-01-30 | Atochem Elf Deutschland | Copolyamid, Verfahren zur Herstellung einer Polyamidfolie und Verwendung der Folie als Heißschmelzklebefolie |
| DE19537614C3 (de) * | 1995-10-09 | 2003-10-02 | Inventa Ag | Polycaprolactam mit neuartiger Kettenregelung |
| DE10022701B4 (de) * | 2000-05-10 | 2006-03-23 | Ems-Chemie Ag | Niedrigschmelzende Copolyamide sowie deren Verwendung als Schmelzklebemittel |
| US20100032629A1 (en) * | 2008-08-07 | 2010-02-11 | Benoit Brule | Adhesive composition containing carbon nanotubes and a copolyamide |
| US20160340472A1 (en) | 2014-01-28 | 2016-11-24 | Radicifil S.P.A. | Three-component copolymers having high transparency and low gas permeability and process for the production thereof |
| FR3026108B1 (fr) * | 2014-09-23 | 2018-07-13 | Arkema France | Composition pour adhesif thermoplastique, adhesif thermoplastique, leurs procedes de fabrication et leurs utilisations |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1348473A (enExample) * | 1962-11-19 | 1964-04-15 | ||
| NL285773A (enExample) * | 1962-11-19 | |||
| JPS5216125B2 (enExample) * | 1972-09-13 | 1977-05-07 |
-
1975
- 1975-03-06 DE DE19752509791 patent/DE2509791A1/de not_active Withdrawn
-
1976
- 1976-02-13 CA CA245,730A patent/CA1076742A/en not_active Expired
- 1976-02-17 US US05/658,527 patent/US4102871A/en not_active Expired - Lifetime
- 1976-02-23 SE SE7602158A patent/SE7602158L/xx unknown
- 1976-03-02 BE BE164778A patent/BE839098A/xx unknown
- 1976-03-03 CH CH267176A patent/CH621136A5/de not_active IP Right Cessation
- 1976-03-04 FR FR7606133A patent/FR2303039A1/fr active Granted
- 1976-03-05 GB GB8864/76A patent/GB1539600A/en not_active Expired
- 1976-03-06 JP JP51023754A patent/JPS51111897A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FR2303039B1 (enExample) | 1979-03-09 |
| JPS51111897A (en) | 1976-10-02 |
| SE7602158L (sv) | 1976-09-07 |
| US4102871A (en) | 1978-07-25 |
| GB1539600A (en) | 1979-01-31 |
| FR2303039A1 (fr) | 1976-10-01 |
| CH621136A5 (enExample) | 1981-01-15 |
| BE839098A (fr) | 1976-09-02 |
| DE2509791A1 (de) | 1976-09-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry | ||
| MKEX | Expiry |
Effective date: 19970429 |