GB1249793A - Polymerization of pivalolactone - Google Patents
Polymerization of pivalolactoneInfo
- Publication number
- GB1249793A GB1249793A GB312770A GB312770A GB1249793A GB 1249793 A GB1249793 A GB 1249793A GB 312770 A GB312770 A GB 312770A GB 312770 A GB312770 A GB 312770A GB 1249793 A GB1249793 A GB 1249793A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pivalolactone
- diluent
- jan
- iodide
- quaternary ammonium
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/82—Preparation processes characterised by the catalyst used
- C08G63/823—Preparation processes characterised by the catalyst used for the preparation of polylactones or polylactides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
1,249,793. Polycondensation of pivalolactone. SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ N.V. 22 Jan., 1970 [24 Jan., 1969], No. 3127/70. Heading C3R. Polyesters are made by polycondensing lactone monomers containing at least 95% by wt. of pivalolactone in a liquid diluent in the presence of, as an initiator, a quaternary ammonium salt which has a solubility in the diluent, at the polymerization temperature of not greater than 50 mgms./100 mls. The diluent is preferably a hydrocarbon. Quaternary ammonium salts of strong mineral acids are preferred and in the examples tetraethylene ammonium chloride, bromide and iodide, and tetrabutyl ammonium iodide are used.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL6901177A NL6901177A (en) | 1969-01-24 | 1969-01-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1249793A true GB1249793A (en) | 1971-10-13 |
Family
ID=19805958
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB312770A Expired GB1249793A (en) | 1969-01-24 | 1970-01-22 | Polymerization of pivalolactone |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE744807A (en) |
CH (1) | CH530431A (en) |
DE (1) | DE2002846A1 (en) |
FR (1) | FR2029042A1 (en) |
GB (1) | GB1249793A (en) |
NL (1) | NL6901177A (en) |
-
1969
- 1969-01-24 NL NL6901177A patent/NL6901177A/xx unknown
-
1970
- 1970-01-22 FR FR7002296A patent/FR2029042A1/fr not_active Withdrawn
- 1970-01-22 GB GB312770A patent/GB1249793A/en not_active Expired
- 1970-01-22 BE BE744807D patent/BE744807A/en unknown
- 1970-01-22 DE DE19702002846 patent/DE2002846A1/en active Pending
- 1970-01-22 CH CH88270A patent/CH530431A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FR2029042A1 (en) | 1970-10-16 |
BE744807A (en) | 1970-07-22 |
CH530431A (en) | 1972-11-15 |
NL6901177A (en) | 1970-07-28 |
DE2002846A1 (en) | 1970-10-01 |
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