DE1745029A1 - Verfahren zur Herstellung von ternaeren Mischpolyamiden - Google Patents
Verfahren zur Herstellung von ternaeren MischpolyamidenInfo
- Publication number
- DE1745029A1 DE1745029A1 DE19681745029 DE1745029A DE1745029A1 DE 1745029 A1 DE1745029 A1 DE 1745029A1 DE 19681745029 DE19681745029 DE 19681745029 DE 1745029 A DE1745029 A DE 1745029A DE 1745029 A1 DE1745029 A1 DE 1745029A1
- Authority
- DE
- Germany
- Prior art keywords
- percent
- weight
- production
- caprolactam
- mixed polyamides
- 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 8
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000004952 Polyamide Substances 0.000 title description 10
- 229920002647 polyamide Polymers 0.000 title description 10
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 18
- UFFRSDWQMJYQNE-UHFFFAOYSA-N 6-azaniumylhexylazanium;hexanedioate Chemical compound [NH3+]CCCCCC[NH3+].[O-]C(=O)CCCCC([O-])=O UFFRSDWQMJYQNE-UHFFFAOYSA-N 0.000 claims description 7
- 229960002684 aminocaproic acid Drugs 0.000 claims description 6
- 229920000299 Nylon 12 Polymers 0.000 claims description 5
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 claims description 4
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 claims description 4
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims description 3
- 229920002292 Nylon 6 Polymers 0.000 claims 1
- 229920002302 Nylon 6,6 Polymers 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 description 7
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- -1 poly aurine lactam Chemical class 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004753 textile Substances 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 |
|---|---|---|---|
| CH358367A CH491150A (de) | 1967-03-13 | 1967-03-13 | Verfahren zur Herstellung von ternären Mischpolyamiden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1745029A1 true DE1745029A1 (de) | 1972-04-13 |
Family
ID=4259114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19681745029 Pending DE1745029A1 (de) | 1967-03-13 | 1968-03-08 | Verfahren zur Herstellung von ternaeren Mischpolyamiden |
Country Status (7)
| Country | Link |
|---|---|
| AT (1) | AT279170B (enExample) |
| BE (1) | BE712009A (enExample) |
| CH (1) | CH491150A (enExample) |
| DE (1) | DE1745029A1 (enExample) |
| ES (1) | ES351485A1 (enExample) |
| FR (1) | FR1574742A (enExample) |
| GB (1) | GB1168404A (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0324773B1 (en) * | 1986-11-24 | 1990-11-22 | AlliedSignal Inc. | Synthetic yarn with heat-activated binder fiber |
| US6969437B1 (en) | 1997-01-30 | 2005-11-29 | Alliedsignal Inc. | Yarn with heat-activated binder material and process of making |
| US6682618B1 (en) | 1986-11-24 | 2004-01-27 | Alliedsignal Inc. | Yarn with heat-activated binder material and process of making |
| CH674518A5 (enExample) | 1987-09-09 | 1990-06-15 | Inventa Ag | |
| US5110641A (en) * | 1990-12-14 | 1992-05-05 | E. I. Du Pont De Nemours And Company | Melt-dispersible package for melt-processible polymers |
| WO1994009196A1 (en) * | 1992-10-14 | 1994-04-28 | Allied-Signal Inc. | Synthetic yarn with heat-activated binder fiber |
| US6658835B1 (en) | 2000-11-28 | 2003-12-09 | Honeywell International Inc. | Untwisted wrapped singles yarns and carpets manufactured therefrom |
| US7261849B2 (en) | 2002-04-30 | 2007-08-28 | Solutia, Inc. | Tacky polymer melt spinning process |
-
1967
- 1967-03-13 CH CH358367A patent/CH491150A/de not_active IP Right Cessation
-
1968
- 1968-03-08 DE DE19681745029 patent/DE1745029A1/de active Pending
- 1968-03-11 ES ES351485A patent/ES351485A1/es not_active Expired
- 1968-03-11 BE BE712009D patent/BE712009A/xx unknown
- 1968-03-12 AT AT242168A patent/AT279170B/de not_active IP Right Cessation
- 1968-03-12 FR FR1574742D patent/FR1574742A/fr not_active Expired
- 1968-03-12 GB GB1198768A patent/GB1168404A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AT279170B (de) | 1970-02-25 |
| FR1574742A (enExample) | 1969-07-18 |
| ES351485A1 (es) | 1969-06-01 |
| BE712009A (enExample) | 1968-09-11 |
| GB1168404A (en) | 1969-10-22 |
| CH491150A (de) | 1970-05-31 |
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