DE1282843B - Fasern und Faeden aus Polyamiden - Google Patents
Fasern und Faeden aus PolyamidenInfo
- Publication number
- DE1282843B DE1282843B DEP20238A DEP0020238A DE1282843B DE 1282843 B DE1282843 B DE 1282843B DE P20238 A DEP20238 A DE P20238A DE P0020238 A DEP0020238 A DE P0020238A DE 1282843 B DE1282843 B DE 1282843B
- Authority
- DE
- Germany
- Prior art keywords
- threads
- fibers
- aromatic
- polymer
- 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
- 239000000835 fiber Substances 0.000 title claims description 30
- 239000004952 Polyamide Substances 0.000 title claims description 16
- 229920002647 polyamide Polymers 0.000 title claims description 16
- 229920000642 polymer Polymers 0.000 claims description 31
- 125000003118 aryl group Chemical group 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 9
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 5
- 239000002904 solvent Substances 0.000 description 24
- 150000001412 amines Chemical class 0.000 description 23
- 238000000034 method Methods 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- -1 aromatic dicarboxylic acids Chemical class 0.000 description 7
- 239000004744 fabric Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 239000004760 aramid Substances 0.000 description 5
- 229920003235 aromatic polyamide Polymers 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 206010061218 Inflammation Diseases 0.000 description 3
- 229920002302 Nylon 6,6 Polymers 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000002657 fibrous material Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 230000004054 inflammatory process Effects 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 229920000889 poly(m-phenylene isophthalamide) Polymers 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 150000003462 sulfoxides Chemical class 0.000 description 3
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000002166 wet spinning Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 238000012695 Interfacial polymerization Methods 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000004984 aromatic diamines Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 238000000578 dry spinning Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 229920006158 high molecular weight polymer Polymers 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- LNWWQYYLZVZXKS-UHFFFAOYSA-N 1-pyrrolidin-1-ylethanone Chemical compound CC(=O)N1CCCC1 LNWWQYYLZVZXKS-UHFFFAOYSA-N 0.000 description 1
- KBLZUSCEBGBILB-UHFFFAOYSA-N 2,2-dimethylthiolane 1,1-dioxide Chemical compound CC1(C)CCCS1(=O)=O KBLZUSCEBGBILB-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- NUIURNJTPRWVAP-UHFFFAOYSA-N 3,3'-Dimethylbenzidine Chemical compound C1=C(N)C(C)=CC(C=2C=C(C)C(N)=CC=2)=C1 NUIURNJTPRWVAP-UHFFFAOYSA-N 0.000 description 1
- YCGKJPVUGMBDDS-UHFFFAOYSA-N 3-(6-azabicyclo[3.1.1]hepta-1(7),2,4-triene-6-carbonyl)benzamide Chemical compound NC(=O)C1=CC=CC(C(=O)N2C=3C=C2C=CC=3)=C1 YCGKJPVUGMBDDS-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- CQPBLBQMIFRGLU-UHFFFAOYSA-N 4-(6-azabicyclo[3.1.1]hepta-1(7),2,4-triene-6-carbonyl)benzamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N1C2=CC=CC1=C2 CQPBLBQMIFRGLU-UHFFFAOYSA-N 0.000 description 1
- ZYEDGEXYGKWJPB-UHFFFAOYSA-N 4-[2-(4-aminophenyl)propan-2-yl]aniline Chemical compound C=1C=C(N)C=CC=1C(C)(C)C1=CC=C(N)C=C1 ZYEDGEXYGKWJPB-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000238557 Decapoda Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 229920001283 Polyalkylene terephthalate Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- VEGZHURRCWERMK-UHFFFAOYSA-N benzene-1,3-diamine;hydrochloride Chemical compound Cl.NC1=CC=CC(N)=C1 VEGZHURRCWERMK-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- VNWKTOKETHGBQD-AKLPVKDBSA-N carbane Chemical compound [15CH4] VNWKTOKETHGBQD-AKLPVKDBSA-N 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229920006015 heat resistant resin Polymers 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- QZUPTXGVPYNUIT-UHFFFAOYSA-N isophthalamide Chemical compound NC(=O)C1=CC=CC(C(N)=O)=C1 QZUPTXGVPYNUIT-UHFFFAOYSA-N 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920003366 poly(p-phenylene terephthalamide) Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000002990 reinforced plastic Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/091—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
-
- 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
- C08G69/32—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids from aromatic diamines and aromatic dicarboxylic acids with both amino and carboxylic groups aromatically bound
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
- D01F6/605—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides from aromatic polyamides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2377/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C08J2377/10—Polyamides derived from aromatically bound amino and carboxyl groups of amino carboxylic acids or of polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Polyamides (AREA)
- Artificial Filaments (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US64292857A | 1957-02-28 | 1957-02-28 | |
| US713304A US3063966A (en) | 1958-02-05 | 1958-02-05 | Process of making wholly aromatic polyamides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1282843B true DE1282843B (de) | 1968-11-14 |
Family
ID=27094145
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19581420681 Pending DE1420681B2 (de) | 1957-02-28 | 1958-02-28 | Verfahren zur herstellung aromatischer polyamide |
| DEP20238A Pending DE1282843B (de) | 1957-02-28 | 1958-02-28 | Fasern und Faeden aus Polyamiden |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19581420681 Pending DE1420681B2 (de) | 1957-02-28 | 1958-02-28 | Verfahren zur herstellung aromatischer polyamide |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE565266A (enrdf_load_stackoverflow) |
| CH (2) | CH426262A (enrdf_load_stackoverflow) |
| DE (2) | DE1420681B2 (enrdf_load_stackoverflow) |
| FR (2) | FR1199458A (enrdf_load_stackoverflow) |
| GB (2) | GB871581A (enrdf_load_stackoverflow) |
| NL (1) | NL108288C (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2219703A1 (de) * | 1971-04-28 | 1972-11-09 | E.I. Du Pont De Nemours And Co., Wilmington, Del. (V.St.A.) | Polyamidfasern und -folien und Verfahren zur Herstellung derselben |
| EP0567998A1 (de) * | 1992-04-30 | 1993-11-03 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von Faserbildenden meta-Aramiden |
| EP0567987A1 (de) * | 1992-04-30 | 1993-11-03 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von Fasern aus meta-Aramiden |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3049518A (en) * | 1960-03-31 | 1962-08-14 | Du Pont | Polyamides from n, n'-bis (3-aminophenyl)-isophthalamide |
| DE1239430B (de) * | 1963-09-18 | 1967-04-27 | Hoechst Ag | Verfahren zur Herstellung von Faeden aus beta-Polyamiden |
| USRE30352E (en) | 1966-06-13 | 1980-07-29 | E. I. Du Pont De Nemours And Company | Optically anisotropic aromatic polyamide dopes |
| DE1745254A1 (de) * | 1966-06-13 | 1970-12-23 | Du Pont | Polyamidfaeden,-fasern,-folien und -fibriden |
| CA928440A (en) * | 1967-12-27 | 1973-06-12 | I. Bair Thomas | Fibres of aromatic para-oriented polyterephthalamides |
| DE1810426B2 (de) * | 1968-06-12 | 1980-08-28 | E.I. Du Pont De Nemours And Co., Wilmington, Del. (V.St.A.) | Aromatische Polyamide enthaltende, optisch anisotrope Masse |
| DE2313308A1 (de) * | 1973-03-17 | 1974-09-19 | Hoechst Ag | Verfahren zur herstellung von faeden, fasern und folien aus aromatischen polyamiden |
| US4162275A (en) * | 1973-07-26 | 1979-07-24 | E. I. Du Pont De Nemours And Company | Flame-resistant fiber |
| US4118374A (en) | 1974-09-09 | 1978-10-03 | Sumitomo Chemical Company, Limited | Production of aromatic polyamides from dicarboxylic acid and diamine |
| AU500143B2 (en) * | 1974-12-27 | 1979-05-10 | Teijin Ltd | Fiber or film-forming copolyamide |
| NL157327C (nl) * | 1975-02-21 | 1984-05-16 | Akzo Nv | Werkwijze ter bereiding van poly-p-fenyleentereftaalamide. |
| JPS5223198A (en) * | 1975-08-15 | 1977-02-21 | Hitachi Ltd | Preparation of aromatic polyether amide resin |
| JPS5569649A (en) * | 1978-11-21 | 1980-05-26 | Teijin Ltd | Aromatic polyamide composition |
| KR950014523B1 (ko) * | 1991-04-29 | 1995-12-05 | 주식회사 코오롱 | 방향족 폴리아미드 펄프 및 그의 제조방법 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB737184A (en) * | 1951-08-29 | 1955-09-21 | Celanese Corp | Production of polyamides |
-
0
- NL NL108288D patent/NL108288C/xx active
-
1958
- 1958-02-27 FR FR1199458D patent/FR1199458A/fr not_active Expired
- 1958-02-27 FR FR1199459D patent/FR1199459A/fr not_active Expired
- 1958-02-28 GB GB6636/58A patent/GB871581A/en not_active Expired
- 1958-02-28 DE DE19581420681 patent/DE1420681B2/de active Pending
- 1958-02-28 CH CH5646258A patent/CH426262A/de unknown
- 1958-02-28 BE BE565266D patent/BE565266A/xx unknown
- 1958-02-28 DE DEP20238A patent/DE1282843B/de active Pending
- 1958-02-28 GB GB6633/58A patent/GB871578A/en not_active Expired
- 1958-02-28 CH CH5646358A patent/CH438572A/de unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB737184A (en) * | 1951-08-29 | 1955-09-21 | Celanese Corp | Production of polyamides |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2219703A1 (de) * | 1971-04-28 | 1972-11-09 | E.I. Du Pont De Nemours And Co., Wilmington, Del. (V.St.A.) | Polyamidfasern und -folien und Verfahren zur Herstellung derselben |
| DE2265806C3 (enrdf_load_stackoverflow) * | 1971-04-28 | 1991-03-07 | E.I. Du Pont De Nemours & Co., Wilmington, Del., Us | |
| EP0567998A1 (de) * | 1992-04-30 | 1993-11-03 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von Faserbildenden meta-Aramiden |
| EP0567987A1 (de) * | 1992-04-30 | 1993-11-03 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von Fasern aus meta-Aramiden |
Also Published As
| Publication number | Publication date |
|---|---|
| CH426262A (de) | 1966-12-15 |
| GB871581A (en) | 1961-06-28 |
| DE1420681A1 (de) | 1968-10-10 |
| NL108288C (enrdf_load_stackoverflow) | |
| GB871578A (en) | 1961-06-28 |
| BE565266A (enrdf_load_stackoverflow) | 1958-08-28 |
| DE1420681B2 (de) | 1971-09-30 |
| CH438572A (de) | 1967-06-30 |
| FR1199459A (fr) | 1959-12-14 |
| FR1199458A (fr) | 1959-12-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1282843B (de) | Fasern und Faeden aus Polyamiden | |
| EP0678539A2 (de) | Aromatische Copolyamide, Verfahren zu deren Herstellung, geformte Gebilde und deren Herstellung | |
| DE3007063A1 (de) | Aromatisches copolyamid und verfahren zu seiner herstellung | |
| DE1570890A1 (de) | Polymerisate aus Diaminobenzaniliden | |
| DE1807144A1 (de) | Fibrillierter Faden | |
| EP0364892A2 (de) | Vollaromatische Polyamide, Verfahren zu ihrer Herstellung und daraus geformte Gebilde | |
| DE3835441A1 (de) | Vollaromatische polyamide, verfahren zu ihrer herstellung und daraus geformte gebilde | |
| EP0396020A2 (de) | Fasermaterialien aus homogenen Legierungen aus aromatischen Polyamiden und Poly-N-Vinyl-pyrrolidon, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE2454118C2 (de) | Verfahren zur Herstellung eines hydrophilen Blockcopolymeren und dessen Verwendung | |
| DE2144126C3 (de) | Hochmolekulare aromatische Polyamide und Fäden aus ihnen | |
| DE3835405A1 (de) | Vollaromatische polyamide, verfahren zu ihrer herstellung und daraus geformte gebilde | |
| EP0852246A2 (de) | Zusammensetzungen enthaltend aromatische Polyamide und Fullerene, sowie geformte Gebilde daraus | |
| DE68927235T2 (de) | Vollaromatisches Polyamidcopolymer | |
| DE1157393B (de) | Verfahren zur Herstellung von Polyamiden | |
| EP0522418B1 (de) | Aromatische Copolyamide, Verfahren zu ihrer Herstellung und daraus geformte Gebilde | |
| DE1645410A1 (de) | Verfahren zur Herstellung von transparenten Polyamiden | |
| EP0553755A2 (de) | Aromatische Copolyamide, Verfahren zu ihrer Herstellung und daraus geformte Gebilde | |
| DE4004652A1 (de) | Vollaromatische polyamide, verfahren zu ihrer herstellung und daraus geformte gebilde | |
| DE1669518A1 (de) | Kristalline,orientierte Faeden | |
| DE2420530A1 (de) | Verfahren zur herstellung von sulfonatgruppenhaltigen aromatischen polyamiden | |
| DE2347163A1 (de) | Film- und faedenbildende loesungen und daraus erhaltene endlosfaeden | |
| EP0499230B1 (de) | Aromatische Copolyamide, Verfahren zu ihrer Herstellung und daraus geformte Gebilde | |
| DE2530875C3 (de) | Anisotrope Flüssigkeit von Polyamiden mit aromatischen und N-heterocycIischen Einheiten | |
| DE2160118B2 (de) | Verfahren zur herstellung von biaxial gereckter polyamidfolie | |
| DE4411757A1 (de) | Aromatische Copolyamide, Verfahren zu deren Herstellung, geformte Gebilde und deren Herstellung |