DE2103004A1 - Verfahren zur anionischen katalytischen Polymerisation von Lactamen - Google Patents
Verfahren zur anionischen katalytischen Polymerisation von LactamenInfo
- Publication number
- DE2103004A1 DE2103004A1 DE19712103004 DE2103004A DE2103004A1 DE 2103004 A1 DE2103004 A1 DE 2103004A1 DE 19712103004 DE19712103004 DE 19712103004 DE 2103004 A DE2103004 A DE 2103004A DE 2103004 A1 DE2103004 A1 DE 2103004A1
- Authority
- DE
- Germany
- Prior art keywords
- lactam
- groups
- accelerators
- etherified
- lactams
- 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
- 150000003951 lactams Chemical class 0.000 title claims description 27
- 238000006116 polymerization reaction Methods 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 11
- 125000000129 anionic group Chemical group 0.000 title claims description 8
- 230000003197 catalytic effect Effects 0.000 title claims description 7
- 229920000570 polyether Polymers 0.000 claims description 18
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 16
- 239000004952 Polyamide Substances 0.000 claims description 15
- 229920002647 polyamide Polymers 0.000 claims description 15
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 8
- 230000000694 effects Effects 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 5
- 238000002474 experimental method Methods 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- -1 styrene isobutylene-N-vinyl succinimide Chemical compound 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 230000003750 conditioning effect Effects 0.000 description 4
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 2
- QISSLHPKTCLLDL-UHFFFAOYSA-N N-Acetylcaprolactam Chemical compound CC(=O)N1CCCCCC1=O QISSLHPKTCLLDL-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 2
- UYGTVQNSPBEEPR-UHFFFAOYSA-N [5-(2-amino-6-oxo-3h-purin-9-yl)-3,3-dimethylpentyl]phosphonic acid Chemical compound N1C(N)=NC(=O)C2=C1N(CCC(C)(C)CCP(O)(O)=O)C=N2 UYGTVQNSPBEEPR-UHFFFAOYSA-N 0.000 description 2
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000006266 etherification reaction Methods 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- FCFWEOGTZZPCTO-QMMMGPOBSA-N (2s)-3,6-dimethoxy-2-propan-2-yl-2,5-dihydropyrazine Chemical compound COC1=N[C@@H](C(C)C)C(OC)=NC1 FCFWEOGTZZPCTO-QMMMGPOBSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- 229920002755 poly(epichlorohydrin) Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- AZWIBRSRBIVSHB-UHFFFAOYSA-N prop-2-enoyl chloride styrene Chemical compound ClC(=O)C=C.C=CC1=CC=CC=C1 AZWIBRSRBIVSHB-UHFFFAOYSA-N 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL7001021A NL7001021A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1970-01-24 | 1970-01-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2103004A1 true DE2103004A1 (de) | 1971-08-05 |
Family
ID=19809168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712103004 Pending DE2103004A1 (de) | 1970-01-24 | 1971-01-22 | Verfahren zur anionischen katalytischen Polymerisation von Lactamen |
Country Status (8)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0099058A1 (de) * | 1982-07-06 | 1984-01-25 | BASF Aktiengesellschaft | Verfahren zur Herstellung von schrumpfarmen Polyamid-Formkörpern |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4501821A (en) * | 1983-07-28 | 1985-02-26 | Ppg Industries, Inc. | Property enhancement of anionically polymerized nylon with dual initiators |
| US4578447A (en) * | 1983-12-28 | 1986-03-25 | Ex-Cell-O Corporation | Rim nylon-based urethane block polymer composition |
| US5290865A (en) * | 1988-10-15 | 1994-03-01 | Sumitomo Chemical Company, Ltd. | Process for producing a lactam compound graft copolymer of ethylene copolymer |
| US4980419A (en) * | 1989-07-03 | 1990-12-25 | Gaf Chemicals Corporation | Alkyl vinyl ether polymers containing a lactam functionality |
| US9006381B2 (en) | 2010-06-23 | 2015-04-14 | Nagase Chemtex Corporation | Impact-resistant polyamide composition and process for production of same |
| EP3626788A1 (en) | 2015-02-05 | 2020-03-25 | Stratasys Ltd. | Digitally-controlled three-dimensional printing of polymerizable materials |
| JP7048502B2 (ja) | 2016-02-05 | 2022-04-05 | ストラタシス リミテッド | ポリアミド形成材料を使用する三次元インクジェット印刷 |
| CN115746557B (zh) * | 2022-12-21 | 2024-07-05 | 无锡殷达尼龙有限公司 | 一种增韧长碳链尼龙及其制备方法与应用 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL295605A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1963-04-04 | |||
| GB1126211A (en) * | 1965-01-14 | 1968-09-05 | Courtaulds Ltd | Improvements in the manufacture of shaped bodies of nylon 6 |
-
1970
- 1970-01-24 NL NL7001021A patent/NL7001021A/xx unknown
-
1971
- 1971-01-21 BE BE761835A patent/BE761835A/xx unknown
- 1971-01-21 US US00108583A patent/US3770689A/en not_active Expired - Lifetime
- 1971-01-22 CH CH99471A patent/CH548429A/xx not_active IP Right Cessation
- 1971-01-22 DE DE19712103004 patent/DE2103004A1/de active Pending
- 1971-01-22 FR FR7102135A patent/FR2085577A1/fr not_active Withdrawn
- 1971-01-25 JP JP46002341A patent/JPS4941354B1/ja active Pending
- 1971-04-19 GB GB2312271*A patent/GB1332405A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0099058A1 (de) * | 1982-07-06 | 1984-01-25 | BASF Aktiengesellschaft | Verfahren zur Herstellung von schrumpfarmen Polyamid-Formkörpern |
Also Published As
| Publication number | Publication date |
|---|---|
| NL7001021A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-07-27 |
| US3770689A (en) | 1973-11-06 |
| GB1332405A (en) | 1973-10-03 |
| CH548429A (de) | 1974-04-30 |
| FR2085577A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-12-24 |
| JPS4941354B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-11-08 |
| BE761835A (fr) | 1971-07-22 |
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