CA1071348A - Compositions a base de copolymeres arylaliphatiques et articles obtenus a partir de ces compositions - Google Patents
Compositions a base de copolymeres arylaliphatiques et articles obtenus a partir de ces compositionsInfo
- Publication number
- CA1071348A CA1071348A CA227,637A CA227637A CA1071348A CA 1071348 A CA1071348 A CA 1071348A CA 227637 A CA227637 A CA 227637A CA 1071348 A CA1071348 A CA 1071348A
- Authority
- CA
- Canada
- Prior art keywords
- radicals
- copolyamide
- trans
- units
- presents
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 53
- 229920001577 copolymer Polymers 0.000 title description 6
- 239000000835 fiber Substances 0.000 claims abstract description 8
- 239000012528 membrane Substances 0.000 claims abstract description 5
- 239000010408 film Substances 0.000 claims abstract description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 36
- 229920000642 polymer Polymers 0.000 claims description 23
- 239000012530 fluid Substances 0.000 claims description 11
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 9
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 241000238876 Acari Species 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims 1
- 230000000306 recurrent effect Effects 0.000 claims 1
- 239000002131 composite material Substances 0.000 abstract description 2
- 239000004744 fabric Substances 0.000 abstract description 2
- 239000004753 textile Substances 0.000 abstract description 2
- 230000002787 reinforcement Effects 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 238000001125 extrusion Methods 0.000 description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 17
- 238000005406 washing Methods 0.000 description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 12
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 12
- 238000001035 drying Methods 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 150000004985 diamines Chemical class 0.000 description 9
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 9
- 238000004804 winding Methods 0.000 description 9
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 8
- 230000003287 optical effect Effects 0.000 description 8
- 150000001805 chlorine compounds Chemical class 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- -1 polymethylene Polymers 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 6
- PWAXUOGZOSVGBO-UHFFFAOYSA-N adipoyl chloride Chemical compound ClC(=O)CCCCC(Cl)=O PWAXUOGZOSVGBO-UHFFFAOYSA-N 0.000 description 6
- 238000013019 agitation Methods 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000015271 coagulation Effects 0.000 description 5
- 238000005345 coagulation Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000002798 polar solvent Substances 0.000 description 5
- 238000006068 polycondensation reaction Methods 0.000 description 5
- QIKYZXDTTPVVAC-UHFFFAOYSA-N 4-Aminobenzamide Chemical compound NC(=O)C1=CC=C(N)C=C1 QIKYZXDTTPVVAC-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 239000004760 aramid Substances 0.000 description 3
- 229920003235 aromatic polyamide Polymers 0.000 description 3
- 239000000701 coagulant Substances 0.000 description 3
- 230000001112 coagulating effect Effects 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- QZLPDBKEVWFQNF-UHFFFAOYSA-N n,n'-diphenylhexanediamide Chemical compound C=1C=CC=CC=1NC(=O)CCCCC(=O)NC1=CC=CC=C1 QZLPDBKEVWFQNF-UHFFFAOYSA-N 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 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
- 241000708948 Solva Species 0.000 description 2
- TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical compound C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 description 2
- 125000005569 butenylene group Chemical group 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920003366 poly(p-phenylene terephthalamide) Polymers 0.000 description 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 2
- 229940116269 uric acid Drugs 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 241000331231 Amorphocerini gen. n. 1 DAD-2008 Species 0.000 description 1
- 241001338801 Chlorus Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 208000001840 Dandruff Diseases 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241001024304 Mino Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000004522 Pentaglottis sempervirens Nutrition 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 229920006018 co-polyamide Polymers 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000003651 hexanedioyl group Chemical group C(CCCCC(=O)*)(=O)* 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 230000002535 lyotropic effect Effects 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
- TWXDDNPPQUTEOV-FVGYRXGTSA-N methamphetamine hydrochloride Chemical compound Cl.CN[C@@H](C)CC1=CC=CC=C1 TWXDDNPPQUTEOV-FVGYRXGTSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 230000010494 opalescence Effects 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 238000005375 photometry Methods 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910021489 α-quartz Inorganic materials 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/30—Sulfur-, selenium- or tellurium-containing compounds
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Artificial Filaments (AREA)
- Polyamides (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Woven Fabrics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7418524A FR2272118B1 (en, 2012) | 1974-05-24 | 1974-05-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1071348A true CA1071348A (fr) | 1980-02-05 |
Family
ID=9139371
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA227,637A Expired CA1071348A (fr) | 1974-05-24 | 1975-05-23 | Compositions a base de copolymeres arylaliphatiques et articles obtenus a partir de ces compositions |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US4231913A (en, 2012) |
| JP (1) | JPS5911609B2 (en, 2012) |
| BE (1) | BE829431A (en, 2012) |
| BR (1) | BR7503257A (en, 2012) |
| CA (1) | CA1071348A (en, 2012) |
| CH (1) | CH613221A5 (en, 2012) |
| DD (1) | DD120459A5 (en, 2012) |
| DE (1) | DE2522919A1 (en, 2012) |
| DK (1) | DK227775A (en, 2012) |
| ES (1) | ES437898A1 (en, 2012) |
| FR (1) | FR2272118B1 (en, 2012) |
| GB (1) | GB1501287A (en, 2012) |
| IE (1) | IE41833B1 (en, 2012) |
| IT (1) | IT1038439B (en, 2012) |
| LU (1) | LU72573A1 (en, 2012) |
| NL (2) | NL174730B (en, 2012) |
| SU (1) | SU649330A3 (en, 2012) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0005913B2 (en) * | 1978-05-26 | 1991-10-30 | Imperial Chemical Industries Plc | Method of improving the processability of rigid polymers; melts, solutions and shaped articles prepared according to this method |
| JPS57130A (en) * | 1980-05-30 | 1982-01-05 | Unitika Ltd | Melt-moldable copolyamide having aromatic amide unit |
| US4393196A (en) * | 1981-03-02 | 1983-07-12 | Polaroid Corporation | Polymers containing recurring units from dienoic acid |
| US4461887A (en) * | 1981-03-02 | 1984-07-24 | Polaroid Corporation | Birefringent polymer containing recurring units from dienoic acid |
| US4359568A (en) * | 1981-05-20 | 1982-11-16 | The United States Of America As Represented By The Secretary Of The Air Force | Polyaromatic amides containing 1,3-butadiene units |
| US4511709A (en) * | 1981-10-20 | 1985-04-16 | Korea Advanced Institute Of Science And Technology | Wholly aromatic or aliphatic aromatic block copolyamides and process therefor |
| JPS59187054A (ja) * | 1983-04-06 | 1984-10-24 | Toray Ind Inc | 耐熱性熱可塑性樹脂組成物 |
| US4556697A (en) * | 1983-07-25 | 1985-12-03 | The Standard Oil Company | Alternating copolyamide prepared on a polymer matrix |
| KR860000729B1 (ko) * | 1984-02-06 | 1986-06-14 | 한국과학 기술원 | 구조 단위가 규칙적으로 배열된 방향족-지방족 공중합 폴리아미드 섬유의 제조방법 |
| JPS62293496A (ja) * | 1986-06-12 | 1987-12-21 | 松下電器産業株式会社 | 電気器具の表示装置 |
| US5102601A (en) * | 1986-08-25 | 1992-04-07 | Farris Richard J | Process for fabricating novel compostes based on reinforcement with microfibrillar networks of rigid-rod polymers |
| US4842924A (en) * | 1986-08-25 | 1989-06-27 | Farris Richard J | Novel compositions based on reinforcement with microfibrillar networks of rigid-rod polymers |
| US4822669A (en) * | 1987-08-21 | 1989-04-18 | Colgate-Palmolive Company | Absorbent floor mat |
| US4954578A (en) * | 1988-10-25 | 1990-09-04 | International Business Machines Corporation | Fine domain composite films of polyimide mixtures |
| US5331053A (en) * | 1990-12-14 | 1994-07-19 | E. I. Du Pont De Nemours And Company | Fibrid reinforced elastomers |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2174619A (en) * | 1936-09-22 | 1939-10-03 | Du Pont | Polyamides |
| US3063966A (en) * | 1958-02-05 | 1962-11-13 | Du Pont | Process of making wholly aromatic polyamides |
| NL128614C (en, 2012) * | 1962-09-11 | |||
| US3296213A (en) * | 1963-06-19 | 1967-01-03 | Monsanto Co | Aromatic-aliphatic copolyamides |
| US3354125A (en) * | 1963-07-29 | 1967-11-21 | Monsanto Co | Polymers from diaminobenzanilides |
| DE1745254A1 (de) * | 1966-06-13 | 1970-12-23 | Du Pont | Polyamidfaeden,-fasern,-folien und -fibriden |
| US3671542A (en) * | 1966-06-13 | 1972-06-20 | Du Pont | Optically anisotropic aromatic polyamide dopes |
| US3497479A (en) * | 1966-07-29 | 1970-02-24 | Sun Oil Co | Curable polyamides from dimethyl muconic acid isomers |
| US3622545A (en) * | 1969-11-14 | 1971-11-23 | Du Pont | High molecular weight aromatic-aliphatic ordered copolyamides |
| US3600350A (en) * | 1970-04-20 | 1971-08-17 | Du Pont | Poly(p-benzamide) composition,process and product |
| US3673143A (en) * | 1970-06-24 | 1972-06-27 | Du Pont | Optically anisotropic spinning dopes of polycarbonamides |
| IL39187A (en) * | 1971-04-28 | 1976-02-29 | Du Pont | Polyamide fibers and films and their preparation |
| US3770704A (en) * | 1972-03-24 | 1973-11-06 | Monsanto Co | Aromatic polyamides containing 4,4-diamino-oxanilide moieties |
| US3801528A (en) * | 1972-10-27 | 1974-04-02 | Du Pont | Novel polymers and dopes of aromatic polyamides containing a stilbene radical |
| US3804791A (en) * | 1972-10-27 | 1974-04-16 | Du Pont | Polyamide spinning dope |
| US3836498A (en) * | 1972-10-27 | 1974-09-17 | Du Pont | Polyamides and their anisotropic dopes |
-
0
- NL NLAANVRAGE7506101,A patent/NL174730C/xx active
-
1974
- 1974-05-24 FR FR7418524A patent/FR2272118B1/fr not_active Expired
-
1975
- 1975-05-23 CA CA227,637A patent/CA1071348A/fr not_active Expired
- 1975-05-23 IT IT23689/75A patent/IT1038439B/it active
- 1975-05-23 IE IE1152/75A patent/IE41833B1/en unknown
- 1975-05-23 NL NLAANVRAGE7506101,A patent/NL174730B/xx not_active IP Right Cessation
- 1975-05-23 JP JP50062437A patent/JPS5911609B2/ja not_active Expired
- 1975-05-23 BR BR4167/75A patent/BR7503257A/pt unknown
- 1975-05-23 BE BE156659A patent/BE829431A/xx not_active IP Right Cessation
- 1975-05-23 DE DE19752522919 patent/DE2522919A1/de active Granted
- 1975-05-23 CH CH662775A patent/CH613221A5/xx not_active IP Right Cessation
- 1975-05-23 ES ES437898A patent/ES437898A1/es not_active Expired
- 1975-05-23 DK DK227775A patent/DK227775A/da not_active Application Discontinuation
- 1975-05-23 LU LU72573A patent/LU72573A1/xx unknown
- 1975-05-23 SU SU752139552A patent/SU649330A3/ru active
- 1975-05-23 GB GB22638/75A patent/GB1501287A/en not_active Expired
- 1975-05-24 DD DD186242A patent/DD120459A5/xx unknown
-
1978
- 1978-03-28 US US05/890,992 patent/US4231913A/en not_active Expired - Lifetime
-
1980
- 1980-05-23 US US06/152,816 patent/US4309531A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| GB1501287A (en) | 1978-02-15 |
| NL174730C (nl) | |
| DK227775A (da) | 1975-11-25 |
| BE829431A (fr) | 1975-11-24 |
| DE2522919A1 (de) | 1975-12-04 |
| US4231913A (en) | 1980-11-04 |
| DD120459A5 (en, 2012) | 1976-06-12 |
| IE41833L (en) | 1975-11-24 |
| BR7503257A (pt) | 1977-02-23 |
| IE41833B1 (en) | 1980-04-09 |
| NL174730B (nl) | 1984-03-01 |
| LU72573A1 (en, 2012) | 1975-10-08 |
| DE2522919C2 (en, 2012) | 1988-08-04 |
| FR2272118B1 (en, 2012) | 1979-05-11 |
| SU649330A3 (ru) | 1979-02-25 |
| JPS511593A (en, 2012) | 1976-01-08 |
| NL7506101A (nl) | 1975-11-26 |
| US4309531A (en) | 1982-01-05 |
| JPS5911609B2 (ja) | 1984-03-16 |
| ES437898A1 (es) | 1977-01-01 |
| FR2272118A1 (en, 2012) | 1975-12-19 |
| CH613221A5 (en, 2012) | 1979-09-14 |
| IT1038439B (it) | 1979-11-20 |
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