JPS61123631A - 芳香族ポリアミド共重合体の製造法 - Google Patents
芳香族ポリアミド共重合体の製造法Info
- Publication number
- JPS61123631A JPS61123631A JP24252284A JP24252284A JPS61123631A JP S61123631 A JPS61123631 A JP S61123631A JP 24252284 A JP24252284 A JP 24252284A JP 24252284 A JP24252284 A JP 24252284A JP S61123631 A JPS61123631 A JP S61123631A
- Authority
- JP
- Japan
- Prior art keywords
- aromatic
- formula
- aromatic polyamide
- polyamide copolymer
- residues
- 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.)
- Granted
Links
- 239000004760 aramid Substances 0.000 title claims description 23
- 229920003235 aromatic polyamide Polymers 0.000 title claims description 23
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 125000003118 aryl group Chemical group 0.000 claims abstract description 32
- 150000001875 compounds Chemical group 0.000 claims abstract description 11
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 6
- 150000001408 amides Chemical class 0.000 claims abstract description 5
- 239000002904 solvent Substances 0.000 claims abstract description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 abstract description 20
- 229920001577 copolymer Polymers 0.000 abstract description 15
- LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 abstract description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical group CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 description 21
- 238000000034 method Methods 0.000 description 14
- 239000000835 fiber Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 150000004984 aromatic diamines Chemical group 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- -1 aromatic dicarboxylic acids Chemical class 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 229920005603 alternating copolymer Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 238000002166 wet spinning Methods 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- FJVIHKKXPLPDSV-UHFFFAOYSA-N 4-phenoxybenzene-1,2-diamine Chemical compound C1=C(N)C(N)=CC=C1OC1=CC=CC=C1 FJVIHKKXPLPDSV-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 235000008708 Morus alba Nutrition 0.000 description 1
- 240000000249 Morus alba Species 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- MHABMANUFPZXEB-UHFFFAOYSA-N O-demethyl-aloesaponarin I Natural products O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=C(O)C(C(O)=O)=C2C MHABMANUFPZXEB-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000002585 base Substances 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
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000004989 dicarbonyl group Chemical group 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Polyamides (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24252284A JPS61123631A (ja) | 1984-11-19 | 1984-11-19 | 芳香族ポリアミド共重合体の製造法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24252284A JPS61123631A (ja) | 1984-11-19 | 1984-11-19 | 芳香族ポリアミド共重合体の製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61123631A true JPS61123631A (ja) | 1986-06-11 |
| JPH0449571B2 JPH0449571B2 (enrdf_load_stackoverflow) | 1992-08-11 |
Family
ID=17090356
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24252284A Granted JPS61123631A (ja) | 1984-11-19 | 1984-11-19 | 芳香族ポリアミド共重合体の製造法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61123631A (enrdf_load_stackoverflow) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0913421A1 (en) * | 1997-10-27 | 1999-05-06 | Teijin Limited | Biaxially oriented film and magnetic recording medium comprising the same as a base film |
| JP2014521805A (ja) * | 2011-07-29 | 2014-08-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アラミド共重合体 |
| JP2014521777A (ja) * | 2011-07-29 | 2014-08-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アラミド共重合体の製造方法 |
| JP2014521804A (ja) * | 2011-07-29 | 2014-08-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アラミド共重合体の製造方法 |
| JP2014524968A (ja) * | 2011-07-29 | 2014-09-25 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アラミド共重合体の製造方法 |
| WO2016052705A1 (ja) * | 2014-10-01 | 2016-04-07 | 株式会社ブリヂストン | タイヤ骨格体およびタイヤ |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51131595A (en) * | 1975-05-13 | 1976-11-16 | Toyobo Co Ltd | A process for preparing aliphatic-aromatic polyamide |
| JPS53143725A (en) * | 1977-05-17 | 1978-12-14 | Nissan Chem Ind Ltd | Spinning of polypiperazine phthalamide |
| JPS5496A (en) * | 1977-04-27 | 1979-01-05 | Rhone Poulenc Textile | Method of continuously making polyamides derived from paraaphenylene diamine |
-
1984
- 1984-11-19 JP JP24252284A patent/JPS61123631A/ja active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51131595A (en) * | 1975-05-13 | 1976-11-16 | Toyobo Co Ltd | A process for preparing aliphatic-aromatic polyamide |
| JPS5496A (en) * | 1977-04-27 | 1979-01-05 | Rhone Poulenc Textile | Method of continuously making polyamides derived from paraaphenylene diamine |
| JPS53143725A (en) * | 1977-05-17 | 1978-12-14 | Nissan Chem Ind Ltd | Spinning of polypiperazine phthalamide |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0913421A1 (en) * | 1997-10-27 | 1999-05-06 | Teijin Limited | Biaxially oriented film and magnetic recording medium comprising the same as a base film |
| US6180254B1 (en) | 1997-10-27 | 2001-01-30 | Teijin Limited | Biaxially oriented film and magnetic recording medium comprising the same as a base film |
| JP2014521805A (ja) * | 2011-07-29 | 2014-08-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アラミド共重合体 |
| JP2014521777A (ja) * | 2011-07-29 | 2014-08-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アラミド共重合体の製造方法 |
| JP2014521804A (ja) * | 2011-07-29 | 2014-08-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アラミド共重合体の製造方法 |
| JP2014524968A (ja) * | 2011-07-29 | 2014-09-25 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アラミド共重合体の製造方法 |
| WO2016052705A1 (ja) * | 2014-10-01 | 2016-04-07 | 株式会社ブリヂストン | タイヤ骨格体およびタイヤ |
| JP5989279B1 (ja) * | 2014-10-01 | 2016-09-07 | 株式会社ブリヂストン | タイヤ骨格体およびタイヤ |
| US10059808B2 (en) | 2014-10-01 | 2018-08-28 | Bridgestone Corporation | Tire skeleton and tire |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0449571B2 (enrdf_load_stackoverflow) | 1992-08-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4075172A (en) | Novel aromatic copolyamides prepared from 3,4' diphenylene type diamines, and shaped articles therefrom | |
| US3063966A (en) | Process of making wholly aromatic polyamides | |
| US3354127A (en) | Aromatic copolyamides | |
| JPS6139976B2 (enrdf_load_stackoverflow) | ||
| US4507467A (en) | Wholly aromatic halogenated polyamide fiber and film | |
| JPH07300534A (ja) | 特定の成形溶液を用いる繊維またはフィルムの製造方法、および、それによって得ることの可能な繊維またはフィルム | |
| US5093464A (en) | Wholly aromatic polyamide from N,N'-bis (4-amino phenyl)-isophthalamide | |
| JPH06500147A (ja) | 芳香族コポリアミド，それらの製法、および造形構造物の製造のためのそれらの使用 | |
| JPH03153734A (ja) | 芳香族コポリアミドとその製造法 | |
| JPS61123631A (ja) | 芳香族ポリアミド共重合体の製造法 | |
| US5274071A (en) | Wholly aromatic polyamide | |
| Imai et al. | Preparation and properties of N‐phenylated aromatic polyamides from N, N′‐diphenyl‐p‐phenylenediamine and aromatic diacid chlorides | |
| Liaw et al. | Synthesis and characterization of new soluble polyamides containing ether and pendant cyclododecylidene groups | |
| US5543492A (en) | Hydrolysis-resistant aramids | |
| JPH0680775A (ja) | 繊維形成用メタ−アラミドの調製 | |
| US4371690A (en) | Heat-resistant rigid polymers from difunctional 9,10-dihydro-9,10-ethanoanthracenes | |
| CA1329299C (en) | Thermoplastically processible aromatic polyetheramide, process for its production and its use for the production of moldings | |
| JPH02263829A (ja) | 新規芳香族コポリアミド及びその製法 | |
| US4914180A (en) | Polyamides prepared from 2-(3-aminophenyl)-2-(4-aminophenyl) hexafluoro propane | |
| US3842028A (en) | Process for preparing spinning solutions of polyhydrazides | |
| US4373087A (en) | O-Tolidine sulfone based copolyamide fiber | |
| US4794159A (en) | Heat-resistant polyamide from bis(4-aminophenyl)fluorene | |
| JPS6234848B2 (enrdf_load_stackoverflow) | ||
| US3335114A (en) | Polycarbonamides from p-phenylenebis(dimethylacetic acid) and its derivatives | |
| JPH0331730B2 (enrdf_load_stackoverflow) |