GB798004A - Polybenzimidazoles and method of preparing the same - Google Patents
Polybenzimidazoles and method of preparing the sameInfo
- Publication number
- GB798004A GB798004A GB32329/56A GB3232956A GB798004A GB 798004 A GB798004 A GB 798004A GB 32329/56 A GB32329/56 A GB 32329/56A GB 3232956 A GB3232956 A GB 3232956A GB 798004 A GB798004 A GB 798004A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- diaminophenyl
- polybenzimidazoles
- propane
- acid
- 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
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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/18—Polybenzimidazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Abstract
Polybenzimidazoles are made by condensing a bis-diaminophenyl compound with an equimolecular quantity of a dicarboxylic acid at a temperature of from 100 DEG to 350 DEG C. in the absence of oxygen. Preferred bis-diaminophenyl compounds are of the general formula <FORM:0798004/IV (a)/1> where R is a carbon to carbon bond or a divalent hydrocarbon radical, e.g. 1,2-bis(3,4-diaminophenyl) ethane and 2,2-bis-(3,4-diaminophenyl) propane. Preferred dicarboxylic acids are those of the formula HOOC-R1-COOH, where R1 is a chain of methylene groups, e.g. adipic and sebacic acids. The examples describe the preparation of polybenzimidazoles form (1) sebacic acid and 3,31-diaminobenzidine, (2) sebacic acid and 1,2-bis-(3,4-diaminophenyl) ethane, (3) adipic acid and 2,2-bis-(3,4-diaminophenyl) propane and (4) sebacic acid and 2,2-bis-(3,4-diaminophenyl) propane. The polybenzimidazoles may be modified by reaction with diamines. The products may be used as fibres, coatings and mouldings. Specifications 461,236 and 461,237, [both in Group IV], are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US798004XA | 1955-10-28 | 1955-10-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB798004A true GB798004A (en) | 1958-07-09 |
Family
ID=22152901
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32329/56A Expired GB798004A (en) | 1955-10-28 | 1956-10-23 | Polybenzimidazoles and method of preparing the same |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB798004A (en) |
-
1956
- 1956-10-23 GB GB32329/56A patent/GB798004A/en not_active Expired
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