GB734456A - Improvements relating to the production of polyamides - Google Patents
Improvements relating to the production of polyamidesInfo
- Publication number
- GB734456A GB734456A GB1429353A GB1429353A GB734456A GB 734456 A GB734456 A GB 734456A GB 1429353 A GB1429353 A GB 1429353A GB 1429353 A GB1429353 A GB 1429353A GB 734456 A GB734456 A GB 734456A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- polymerized
- polymer
- caprolactam
- minutes
- 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
- 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
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/14—Lactams
- C08G69/16—Preparatory processes
- C08G69/18—Anionic polymerisation
- C08G69/20—Anionic polymerisation characterised by the catalysts used
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
Abstract
Epsilon-caprolactam is polymerized in the presence as catalyst of an alkali metal hydride. Polymerization is complete in 3-10 minutes at 230-255 DEG C., further heating degrading the polymer. Low polymerization temperatures favour high intrinsic viscosities and high temperatures rapidity of polymerization. The polymers formed at low temperatures contain smaller quantities of water extractables. The cyclic amide should have a water content below about 0.02 per cent. In examples (1) e -caprolactam containing 0.005 per cent water was polymerized at 255 DEG C. in an atmosphere of nitrogen using 0.5 mol. per cent of lithium hydride. The intrinsic viscosity of the polymer varied from 2.28 for a heating time of 5 minutes to 0.78 for a heating time of 8 hours. The polymer was powdered and extruded into a film which remained clear on longitudinal stretching. (2)e -caprolacta was polymerized at 255 DEG C. in 4-5 minutes in the presence of 0.5 mol. per cent of lithium hydride, the polymer having an intrinsic viscosity of about 1.02. (3) Samples of e -caprolactam were polymerized in the presence of 0.5 mol. per cent of lithium hydride at various temperatures and over different periods of time. Figures are given for the intrinsic viscosities of the resulting polymers and their content of water extractables. (4) e -caprolactam was polymerized at 255 DEG C. in 7 minutes in the presence of sodium hydride, the polymer having an intrinsic viscosity of 1.40 and containing about 10.5 per cent of water extractables.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US248455A US2647105A (en) | 1951-09-26 | 1951-09-26 | Process of polymerizing epsiloncaprolactam |
GB1429353A GB734456A (en) | 1953-05-21 | 1953-05-21 | Improvements relating to the production of polyamides |
FR1078094D FR1078094A (en) | 1953-05-21 | 1953-06-05 | Improvements in the manufacture of polyamides |
DEP9920A DE972445C (en) | 1953-05-21 | 1953-06-11 | Process for the production of polyamides |
BE520952D BE520952A (en) | 1953-05-21 | 1953-06-25 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1429353A GB734456A (en) | 1953-05-21 | 1953-05-21 | Improvements relating to the production of polyamides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB734456A true GB734456A (en) | 1955-08-03 |
Family
ID=10038557
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1429353A Expired GB734456A (en) | 1951-09-26 | 1953-05-21 | Improvements relating to the production of polyamides |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE520952A (en) |
FR (1) | FR1078094A (en) |
GB (1) | GB734456A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006053076A2 (en) * | 2004-11-09 | 2006-05-18 | E.I. Dupont De Nemours And Company | Ring opening polymerization of cyclic amides using metal amide and metal alkoxide catalysts |
-
1953
- 1953-05-21 GB GB1429353A patent/GB734456A/en not_active Expired
- 1953-06-05 FR FR1078094D patent/FR1078094A/en not_active Expired
- 1953-06-25 BE BE520952D patent/BE520952A/xx unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006053076A2 (en) * | 2004-11-09 | 2006-05-18 | E.I. Dupont De Nemours And Company | Ring opening polymerization of cyclic amides using metal amide and metal alkoxide catalysts |
WO2006053076A3 (en) * | 2004-11-09 | 2006-12-14 | Du Pont | Ring opening polymerization of cyclic amides using metal amide and metal alkoxide catalysts |
Also Published As
Publication number | Publication date |
---|---|
FR1078094A (en) | 1954-11-15 |
BE520952A (en) | 1953-12-28 |
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