DE1420241B2 - Verfahren zur herstellung von formkoerpern durch polymerisationvon lactamen - Google Patents
Verfahren zur herstellung von formkoerpern durch polymerisationvon lactamenInfo
- Publication number
- DE1420241B2 DE1420241B2 DE19591420241 DE1420241A DE1420241B2 DE 1420241 B2 DE1420241 B2 DE 1420241B2 DE 19591420241 DE19591420241 DE 19591420241 DE 1420241 A DE1420241 A DE 1420241A DE 1420241 B2 DE1420241 B2 DE 1420241B2
- Authority
- DE
- Germany
- Prior art keywords
- polymerization
- caprolactam
- activators
- alkaline
- lactamen
- 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
- 238000000034 method Methods 0.000 title claims description 7
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- 238000006116 polymerization reaction Methods 0.000 title description 20
- 239000012190 activator Substances 0.000 claims description 29
- 150000003951 lactams Chemical class 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000003054 catalyst Substances 0.000 claims description 5
- 238000000465 moulding Methods 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 24
- 239000004952 Polyamide Substances 0.000 description 8
- 239000012948 isocyanate Substances 0.000 description 8
- 150000002513 isocyanates Chemical class 0.000 description 8
- 229920002647 polyamide Polymers 0.000 description 8
- MOMGDEWWZBKDDR-UHFFFAOYSA-M sodium;3,4,5,6-tetrahydro-2h-azepin-7-olate Chemical compound [Na+].O=C1CCCCC[N-]1 MOMGDEWWZBKDDR-UHFFFAOYSA-M 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 235000013877 carbamide Nutrition 0.000 description 4
- 238000012693 lactam polymerization Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- QISSLHPKTCLLDL-UHFFFAOYSA-N N-Acetylcaprolactam Chemical compound CC(=O)N1CCCCCC1=O QISSLHPKTCLLDL-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- YDLSUFFXJYEVHW-UHFFFAOYSA-N azonan-2-one Chemical compound O=C1CCCCCCCN1 YDLSUFFXJYEVHW-UHFFFAOYSA-N 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- DQAKJEWZWDQURW-UHFFFAOYSA-N pyrrolidonecarboxylic acid Chemical compound OC(=O)N1CCCC1=O DQAKJEWZWDQURW-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- KRDJNXNRTUJHRK-UHFFFAOYSA-N 1,3-dimethyl-1,3-bis(phenylcarbamoyl)urea Chemical compound C=1C=CC=CC=1NC(=O)N(C)C(=O)N(C)C(=O)NC1=CC=CC=C1 KRDJNXNRTUJHRK-UHFFFAOYSA-N 0.000 description 1
- NMQQAMXYVWXNQF-UHFFFAOYSA-N 2-oxo-1-phenylazepane-3-carboxamide Chemical compound C1(=CC=CC=C1)N1C(C(CCCC1)C(N)=O)=O NMQQAMXYVWXNQF-UHFFFAOYSA-N 0.000 description 1
- KRMWJYDLDZJRNK-UHFFFAOYSA-N 2-oxo-n-phenylazepane-1-carboxamide Chemical compound C1CCCCC(=O)N1C(=O)NC1=CC=CC=C1 KRMWJYDLDZJRNK-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000003513 alkali Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-N anhydrous cyanic acid Natural products OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000009750 centrifugal casting Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 150000001912 cyanamides Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- -1 nitrogen form alkali salts Chemical class 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000037303 wrinkles Effects 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
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
- C08G69/18—Anionic polymerisation
- C08G69/20—Anionic polymerisation characterised by the catalysts used
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB0053999 | 1959-07-14 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE1420241A1 DE1420241A1 (de) | 1969-02-13 |
| DE1420241B2 true DE1420241B2 (de) | 1972-01-27 |
Family
ID=6970450
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19591420241 Pending DE1420241B2 (de) | 1959-07-14 | 1959-07-14 | Verfahren zur herstellung von formkoerpern durch polymerisationvon lactamen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3304291A (enExample) |
| BE (1) | BE592979A (enExample) |
| CH (1) | CH393741A (enExample) |
| DE (1) | DE1420241B2 (enExample) |
| FR (1) | FR1262436A (enExample) |
| GB (2) | GB900150A (enExample) |
| NL (2) | NL124646C (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0113252A3 (en) * | 1982-12-29 | 1986-07-30 | Toray Industries, Inc. | Process for producing block copolyamide |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1222254B (de) * | 1961-08-31 | 1966-08-04 | Basf Ag | Verfahren zur anionischen Polymerisation von Lactamen |
| NL284553A (enExample) * | 1961-10-20 | |||
| BE627266A (enExample) * | 1962-01-20 | |||
| BE631857A (enExample) * | 1962-05-04 | |||
| US3316221A (en) * | 1963-07-01 | 1967-04-25 | Du Pont | Aromatic ester cocatalysts for lactam polymerization |
| US3216977A (en) * | 1962-12-13 | 1965-11-09 | Du Pont | Anionic polymerization of lactams with methylene oxazolidine-4, 5-dione compounds as activators |
| US3320335A (en) * | 1963-04-22 | 1967-05-16 | Monsanto Co | Process for polymerizing higher lactams in the presence of urethane polymer promoters |
| GB1039113A (en) * | 1964-08-06 | 1966-08-17 | Ucb Sa | New n-substituted lactams |
| US3366608A (en) * | 1965-04-15 | 1968-01-30 | British Celanese | Anionic polymerization of caprolactam |
| US3440227A (en) * | 1966-03-31 | 1969-04-22 | Budd Co | Polymerization of higher lactams |
| US3621001A (en) * | 1967-07-06 | 1971-11-16 | Basf Ag | Accelerating anionic polymerization of lactams |
| DE2507549A1 (de) * | 1974-05-21 | 1975-12-04 | Bhnf Ag | Poly-laurinlactam, verfahren zur herstellung hoeherer poly-lactame und deren verwendung |
| DE2637010A1 (de) | 1976-08-17 | 1978-02-23 | Bayer Ag | Aktivierte anionische polymerisation |
| US4374771A (en) * | 1982-03-08 | 1983-02-22 | American Cyanamid Company | Blocked isocyanate |
| CA1214012A (en) * | 1983-01-27 | 1986-11-18 | Wei-Yeih W. Yang | Rim process using single component composition |
| US4501821A (en) * | 1983-07-28 | 1985-02-26 | Ppg Industries, Inc. | Property enhancement of anionically polymerized nylon with dual initiators |
| US4582879A (en) * | 1984-03-22 | 1986-04-15 | Frisch Kurt C | Reaction injection molding process and reaction injection molded products |
| DE3425318A1 (de) * | 1984-07-10 | 1986-01-16 | Bayer Ag, 5090 Leverkusen | Verzweigte, thermoplastisch verarbeitbare, schlagzaehe polyamide |
| WO2011144602A1 (de) | 2010-05-19 | 2011-11-24 | Basf Se | Quervernetztes polyamid |
| KR20130043205A (ko) | 2010-07-20 | 2013-04-29 | 바스프 에스이 | 마이크로캡슐화된 잠열 축열체 재료를 포함하는 폴리아미드 몰딩 |
| US8957133B2 (en) | 2010-07-20 | 2015-02-17 | Basf Se | Polyamide moldings comprising microencapsulated latent-heat-accumulator material |
| KR101855544B1 (ko) | 2010-10-07 | 2018-05-04 | 바스프 에스이 | 단량체 조성물을 제조하는 방법 및 몰딩된 폴리아미드 부품 제조를 위한 이의 용도 |
| US9139692B2 (en) | 2010-12-03 | 2015-09-22 | Basf Se | Process for polymerizing lactam |
| CN103249761B (zh) * | 2010-12-03 | 2016-08-10 | 巴斯夫欧洲公司 | 交联聚酰胺的方法 |
| EP2460838A1 (de) | 2010-12-03 | 2012-06-06 | Basf Se | Verfahren zur Polymerisation von Lactam |
| CN103649172B (zh) * | 2011-07-05 | 2015-07-01 | 巴斯夫欧洲公司 | 包含内酰胺、活化剂和催化剂的固体颗粒,所述固体颗粒的制备方法以及所述固体颗粒的用途 |
| US8957180B2 (en) | 2011-08-23 | 2015-02-17 | Basf Se | Process for producing moldings |
| KR101956534B1 (ko) | 2011-08-23 | 2019-03-11 | 바스프 에스이 | 성형품의 제조 방법 |
| EP2748228B1 (de) | 2011-08-23 | 2019-10-09 | Basf Se | Verfahren zur herstellung von formkörpern |
| WO2013144132A1 (de) | 2012-03-27 | 2013-10-03 | Basf Se | Verfahren zur herstellung von polyamidformkörpern aus einer polymerisierbaren zusammensetzung mittels rotationsschmelzverfahren |
| US20160068679A1 (en) | 2013-04-04 | 2016-03-10 | Basf Se | Polymerizable lactam composition containing a sulfonated polyaryl sulfone |
| EP3253560B1 (en) | 2015-02-05 | 2019-11-06 | Stratasys Ltd. | Digitally-controlled three-dimensional printing of polymerizable materials |
| EP3411424B1 (en) | 2016-02-05 | 2024-01-10 | Stratasys Ltd. | Three-dimensional inkjet printing using polyamide-forming materials |
| CN109749077A (zh) * | 2018-12-09 | 2019-05-14 | 中山大学 | 一种利用（硫）脲/碱金属化合物催化剂制备高分子量聚酰胺的方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB863859A (en) * | 1956-07-23 | 1961-03-29 | Monsanto Chemicals | Polymerisation of lactams |
| US3017391A (en) * | 1956-12-13 | 1962-01-16 | Monsanto Chemicals | Preparation of polycaprolactam using n-acyl activators |
| US3148174A (en) * | 1958-04-04 | 1964-09-08 | Gen Aniline & Film Corp | Polymerization of pyrrolidone and piperidone employing nu, nu-disubstituted ureas aschain initiators |
| US3086962A (en) * | 1958-10-03 | 1963-04-23 | Monsanto Chemicals | Process for polymerizing higher lactams |
-
0
- BE BE592979D patent/BE592979A/xx unknown
- NL NL253790D patent/NL253790A/xx unknown
- NL NL124646D patent/NL124646C/xx active
-
1959
- 1959-07-14 DE DE19591420241 patent/DE1420241B2/de active Pending
-
1960
- 1960-07-12 GB GB24220/60A patent/GB900150A/en not_active Expired
- 1960-07-12 CH CH795660A patent/CH393741A/de unknown
- 1960-07-13 GB GB24367/60A patent/GB900151A/en not_active Expired
- 1960-07-15 FR FR833021A patent/FR1262436A/fr not_active Expired
-
1965
- 1965-03-22 US US441860A patent/US3304291A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0113252A3 (en) * | 1982-12-29 | 1986-07-30 | Toray Industries, Inc. | Process for producing block copolyamide |
Also Published As
| Publication number | Publication date |
|---|---|
| NL253790A (enExample) | |
| US3304291A (en) | 1967-02-14 |
| CH393741A (de) | 1965-06-15 |
| NL124646C (enExample) | |
| GB900151A (en) | 1962-07-04 |
| FR1262436A (fr) | 1961-05-26 |
| GB900150A (en) | 1962-07-04 |
| DE1420241A1 (de) | 1969-02-13 |
| BE592979A (enExample) |
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