GB1128807A - Aromatic polyamides - Google Patents
Aromatic polyamidesInfo
- Publication number
- GB1128807A GB1128807A GB2162165A GB2162165A GB1128807A GB 1128807 A GB1128807 A GB 1128807A GB 2162165 A GB2162165 A GB 2162165A GB 2162165 A GB2162165 A GB 2162165A GB 1128807 A GB1128807 A GB 1128807A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- acids
- dicarboxylic acid
- dicarboxylic
- specified include
- 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
- 239000004760 aramid Substances 0.000 title abstract 2
- 229920003235 aromatic polyamide Polymers 0.000 title abstract 2
- 239000002253 acid Substances 0.000 abstract 11
- 150000007513 acids Chemical class 0.000 abstract 10
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 5
- 150000004985 diamines Chemical class 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 abstract 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 150000001721 carbon Chemical group 0.000 abstract 3
- 125000002843 carboxylic acid group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- -1 polymethylene Polymers 0.000 abstract 3
- MYEWQUYMRFSJHT-UHFFFAOYSA-N 2-(2-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC=C1S(=O)(=O)C1=CC=CC=C1N MYEWQUYMRFSJHT-UHFFFAOYSA-N 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 abstract 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 150000002009 diols Chemical group 0.000 abstract 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 abstract 2
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 2
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 abstract 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 abstract 1
- SBKWSVXSBIBFLP-UHFFFAOYSA-N 2,5-dichlorobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC(Cl)=CC(C(O)=O)=C1Cl SBKWSVXSBIBFLP-UHFFFAOYSA-N 0.000 abstract 1
- LMOSYFZLPBHEOW-UHFFFAOYSA-N 2,5-dichloroterephthalic acid Chemical compound OC(=O)C1=CC(Cl)=C(C(O)=O)C=C1Cl LMOSYFZLPBHEOW-UHFFFAOYSA-N 0.000 abstract 1
- ZRWAPLTWCQQSAN-UHFFFAOYSA-N 2-methoxybenzene-1,3-dicarboxylic acid Chemical compound COC1=C(C(O)=O)C=CC=C1C(O)=O ZRWAPLTWCQQSAN-UHFFFAOYSA-N 0.000 abstract 1
- VQBBXLZPRXHYBO-UHFFFAOYSA-N 2-methoxyterephthalic acid Chemical compound COC1=CC(C(O)=O)=CC=C1C(O)=O VQBBXLZPRXHYBO-UHFFFAOYSA-N 0.000 abstract 1
- XCSGHNKDXGYELG-UHFFFAOYSA-N 2-phenoxyethoxybenzene Chemical compound C=1C=CC=CC=1OCCOC1=CC=CC=C1 XCSGHNKDXGYELG-UHFFFAOYSA-N 0.000 abstract 1
- MILSYCKGLDDVLM-UHFFFAOYSA-N 2-phenylpropan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)C1=CC=CC=C1 MILSYCKGLDDVLM-UHFFFAOYSA-N 0.000 abstract 1
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 abstract 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 abstract 1
- APLYBKHRTXFIBT-UHFFFAOYSA-N 4-chlorobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=C(Cl)C(C(O)=O)=C1 APLYBKHRTXFIBT-UHFFFAOYSA-N 0.000 abstract 1
- PVQOOTFUAPBPFE-UHFFFAOYSA-N 4-propoxybenzene-1,3-dicarboxylic acid Chemical compound CCCOC1=CC=C(C(O)=O)C=C1C(O)=O PVQOOTFUAPBPFE-UHFFFAOYSA-N 0.000 abstract 1
- POSMIIJADZKUPL-UHFFFAOYSA-N 5-methoxybenzene-1,3-dicarboxylic acid Chemical compound COC1=CC(C(O)=O)=CC(C(O)=O)=C1 POSMIIJADZKUPL-UHFFFAOYSA-N 0.000 abstract 1
- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 abstract 1
- 239000004141 Sodium laurylsulphate Substances 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 abstract 1
- 239000012965 benzophenone Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 229940018564 m-phenylenediamine Drugs 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 abstract 1
- ABMFBCRYHDZLRD-UHFFFAOYSA-N naphthalene-1,4-dicarboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=C(C(O)=O)C2=C1 ABMFBCRYHDZLRD-UHFFFAOYSA-N 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 abstract 1
- 235000017557 sodium bicarbonate Nutrition 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 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
- C08G69/26—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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL133092D NL133092C (enrdf_load_stackoverflow) | 1965-05-21 | ||
| GB2162165A GB1128807A (en) | 1965-05-21 | 1965-05-21 | Aromatic polyamides |
| FR62409A FR1487392A (fr) | 1965-05-21 | 1966-05-20 | Polyamides et leur procédé de fabrication |
| FR62410A FR1480706A (fr) | 1965-05-21 | 1966-05-20 | Polymères de condensation synthétiques, essentiellement linéaires |
| DE19661620882 DE1620882A1 (de) | 1965-05-21 | 1966-05-20 | Verfahren zur Herstellung von aromatischen Polyamiden |
| BE681358D BE681358A (enrdf_load_stackoverflow) | 1965-05-21 | 1966-05-20 | |
| NL6606949A NL6606949A (enrdf_load_stackoverflow) | 1965-05-21 | 1966-05-20 | |
| NL6607006A NL6607006A (enrdf_load_stackoverflow) | 1965-05-21 | 1966-05-20 | |
| DE19661620881 DE1620881A1 (de) | 1965-05-21 | 1966-05-20 | Verfahren zur Herstellung von aromatischen Polyamiden |
| CH739766A CH486512A (de) | 1965-05-21 | 1966-05-23 | Verfahren zur Herstellung von aromatischen Polyamiden |
| CH739866A CH484217A (de) | 1965-05-21 | 1966-05-23 | Verfahren zur Herstellung von aromatischen Polyamiden |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2162165A GB1128807A (en) | 1965-05-21 | 1965-05-21 | Aromatic polyamides |
| GB2162265 | 1965-08-24 | ||
| GB3625865 | 1965-08-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1128807A true GB1128807A (en) | 1968-10-02 |
Family
ID=27258020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2162165A Expired GB1128807A (en) | 1965-05-21 | 1965-05-21 | Aromatic polyamides |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE681358A (enrdf_load_stackoverflow) |
| CH (1) | CH486512A (enrdf_load_stackoverflow) |
| DE (1) | DE1620882A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1128807A (enrdf_load_stackoverflow) |
| NL (2) | NL6606949A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2556883A1 (de) * | 1974-12-27 | 1976-07-01 | Teijin Ltd | Aromatische copolyamide, hieraus gefertigte formgegenstaende und verfahren zu deren herstellung |
| DE3007063A1 (de) * | 1979-02-26 | 1980-08-28 | Teijin Ltd | Aromatisches copolyamid und verfahren zu seiner herstellung |
| CN115873239A (zh) * | 2022-11-11 | 2023-03-31 | 川化集团有限责任公司 | 一种共聚改性pa10t的制备方法及其改性pa10t共聚物 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3526622A1 (de) * | 1985-07-25 | 1987-01-29 | Huels Chemische Werke Ag | Aromatische polyamide und verfahren zu ihrer herstellung |
-
0
- NL NL133092D patent/NL133092C/xx active
-
1965
- 1965-05-21 GB GB2162165A patent/GB1128807A/en not_active Expired
-
1966
- 1966-05-20 NL NL6606949A patent/NL6606949A/xx unknown
- 1966-05-20 DE DE19661620882 patent/DE1620882A1/de active Pending
- 1966-05-20 BE BE681358D patent/BE681358A/xx unknown
- 1966-05-23 CH CH739766A patent/CH486512A/de not_active IP Right Cessation
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2556883A1 (de) * | 1974-12-27 | 1976-07-01 | Teijin Ltd | Aromatische copolyamide, hieraus gefertigte formgegenstaende und verfahren zu deren herstellung |
| DE3007063A1 (de) * | 1979-02-26 | 1980-08-28 | Teijin Ltd | Aromatisches copolyamid und verfahren zu seiner herstellung |
| CN115873239A (zh) * | 2022-11-11 | 2023-03-31 | 川化集团有限责任公司 | 一种共聚改性pa10t的制备方法及其改性pa10t共聚物 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1620882A1 (de) | 1970-05-14 |
| NL133092C (enrdf_load_stackoverflow) | |
| BE681358A (enrdf_load_stackoverflow) | 1966-11-21 |
| CH486512A (de) | 1970-02-28 |
| NL6606949A (enrdf_load_stackoverflow) | 1966-11-22 |
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