GB615884A - Improvements in or relating to the manufacture of linear nitrogen-containing polymers - Google Patents
Improvements in or relating to the manufacture of linear nitrogen-containing polymersInfo
- Publication number
- GB615884A GB615884A GB2251839A GB2251839A GB615884A GB 615884 A GB615884 A GB 615884A GB 2251839 A GB2251839 A GB 2251839A GB 2251839 A GB2251839 A GB 2251839A GB 615884 A GB615884 A GB 615884A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- glycol
- filaments
- tri
- bis
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of 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)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Abstract
Linear polymers of high molecular weight are prepared by reacting a bis chloroformic ester of a glycol with a compound containing as sole reactive radicals two amino groups until the product has film-forming properties. For products of particularly high molecular weight suitable for example for filaments, equivalent proportions of the reactants are used. The bis chloroformic ester may be prepared by treating with carbonyl chloride, a glycol, e.g. ethylene glycol, di-, tri-, tetra- or penta-methylene glycol, or di- or tri-ethylene glycol. Suitable diamines are ethylene and propylene diamine, 1-3-diamino propane, pentamethylene and hexamethylene diamine, 2-5-diamino hexane and phenylene diamines. Reaction may be at normal temperature or heat may be applied especially in the later stages of the reaction. Completion of the reaction may be assisted by reduction of the pressure or by the presence of alkaline materials. Solvent or diluent may be present and may be distilled off in the later reaction stages. Reaction at elevated temperature is preferably performed in nonoxidising atmosphere, e.g. nitrogen. The products may be formed into filaments or films, if desired, with the aid of plasticisers. These materials may be stretched in known manner.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2251839A GB615884A (en) | 1939-08-03 | 1939-08-03 | Improvements in or relating to the manufacture of linear nitrogen-containing polymers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2251839A GB615884A (en) | 1939-08-03 | 1939-08-03 | Improvements in or relating to the manufacture of linear nitrogen-containing polymers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB615884A true GB615884A (en) | 1949-01-13 |
Family
ID=10180667
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2251839A Expired GB615884A (en) | 1939-08-03 | 1939-08-03 | Improvements in or relating to the manufacture of linear nitrogen-containing polymers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB615884A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2660574A (en) * | 1950-08-04 | 1953-11-24 | Celanese Corp | Process for the production of polyurethanes |
US2675360A (en) * | 1952-04-01 | 1954-04-13 | Eastman Kodak Co | Cellulose acetate fibers with improved dyeing properties |
US2757191A (en) * | 1955-08-04 | 1956-07-31 | Du Pont | Polyurethane bis-chloroformates |
US2800464A (en) * | 1952-04-11 | 1957-07-23 | Celanese Corp | Addition of acid to halt polyurethane producing reaction |
US2894935A (en) * | 1956-03-21 | 1959-07-14 | Dow Chemical Co | Method for the preparation of polyurethanes |
-
1939
- 1939-08-03 GB GB2251839A patent/GB615884A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2660574A (en) * | 1950-08-04 | 1953-11-24 | Celanese Corp | Process for the production of polyurethanes |
US2675360A (en) * | 1952-04-01 | 1954-04-13 | Eastman Kodak Co | Cellulose acetate fibers with improved dyeing properties |
US2800464A (en) * | 1952-04-11 | 1957-07-23 | Celanese Corp | Addition of acid to halt polyurethane producing reaction |
US2757191A (en) * | 1955-08-04 | 1956-07-31 | Du Pont | Polyurethane bis-chloroformates |
US2894935A (en) * | 1956-03-21 | 1959-07-14 | Dow Chemical Co | Method for the preparation of polyurethanes |
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