GB1030746A - Aldehyde polymerisation process - Google Patents
Aldehyde polymerisation processInfo
- Publication number
- GB1030746A GB1030746A GB4297064A GB4297064A GB1030746A GB 1030746 A GB1030746 A GB 1030746A GB 4297064 A GB4297064 A GB 4297064A GB 4297064 A GB4297064 A GB 4297064A GB 1030746 A GB1030746 A GB 1030746A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymerization
- initiator
- degradation
- groups
- temperature
- 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
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/06—Catalysts
-
- 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
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/08—Polymerisation of formaldehyde
-
- 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
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/12—Polymerisation of acetaldehyde or cyclic oligomers thereof
-
- 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
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/14—Polymerisation of single aldehydes not provided for in groups C08G2/08 - C08G2/12
-
- 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
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/28—Post-polymerisation treatments
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
A polymeric aldehyde is prepared by polymerizing at least one aldehyde in the presence of a polymerization initiator at a temperature below that at which the initiator would also act as a catalyst for the degradation of the polymer so formed and the initiator is thereafter rendered ineffective as a catalyst for such degradation, the initiator being the product of reacting together equimolar amounts of a N,N-dihydrocarbon substituted amide and a hydride or hydrocarbon derivative of an element of Groups Ia, IIa, IIIa and IVa (other than carbon or silicon) of the Periodic Table according to Mendel<\>aeeff. The polymerization may be effected in the presence of acid contamination provided the amount of acid present does not substantially exceed 3 moles per mole of initiator. After the polymerization and before allowing the product to warm up, the initiator is either extracted with a suitable selective solvent or a weak acid is added, if sufficient is not already present, to render it ineffective as a degradation catalyst on raising the temperature to that at which degradation of the polymer would normally occur. Aldehydes specified are formaldehyde, acetaldehyde, propionaldehyde, n-butyraldehyde, n-valeraldehyde, iso-valeraldehyde, n-caproaldehyde, cyclohexaldehyde, 2-ethyl hexaldehyde, benzaldehyde and phenyl acetaldehyde. The polymerization may be effected in organic solvents that are liquid at the temperature of the polymerization and a number of these are specified. In the examples, the monomers used are acetaldehyde and n-butyraldehyde in the presence of acetic acid and butyric acid respectively, the catalysts being the reaction products of aluminium triethyl with either dimethyl formamide or tetramethyl urea, the solvents toluene alone or mixed with methyl cyclohexane. The polymerization is effected at -78 DEG C., and is terminated by adding n-butanol and acetone before allowing the mixture to warm up to room temperature. Thermal instability of the polymers may be reduced by reacting the polymer with compounds to replace its terminal hydroxyl groups with more stable groups such as carboxylate, by etherification or by the heat treatment described in Specification 980,516. The polymers may be formed into shaped articles such as films, sheets, fibres and filaments. Conventional composition additives may be incorporatedALSO:Catalysts, used for the low temperature polymerization of aldehydes (see Division C3), are made by reacting equimolar amounts of a N, N-dihydrocarbon substituted amide and a hydride or hydrocarbon derivative of an element of groups IA, IIA, IIIA and IVA (other than carbon or silicon) of the periodic table according to Mendel<\>aeeff. In the examples either dimethyl formamide or a toluene solution of tetramethyl urea are added to a solution of aluminium triethyl in a mixture of cyclohexane and toluene.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2270162A GB1026802A (en) | 1962-06-13 | 1962-06-13 | Improved process for the production of polyaldehydes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1030746A true GB1030746A (en) | 1966-05-25 |
Family
ID=10183706
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4297064A Expired GB1030746A (en) | 1962-06-13 | 1962-06-12 | Aldehyde polymerisation process |
GB2252362A Expired GB1030745A (en) | 1962-06-12 | 1962-06-12 | Aldehyde polymerisation process |
GB2270162A Expired GB1026802A (en) | 1962-06-12 | 1962-06-13 | Improved process for the production of polyaldehydes |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2252362A Expired GB1030745A (en) | 1962-06-12 | 1962-06-12 | Aldehyde polymerisation process |
GB2270162A Expired GB1026802A (en) | 1962-06-12 | 1962-06-13 | Improved process for the production of polyaldehydes |
Country Status (3)
Country | Link |
---|---|
BE (2) | BE633470A (en) |
GB (3) | GB1030746A (en) |
NL (2) | NL293837A (en) |
-
0
- BE BE633469D patent/BE633469A/xx unknown
- BE BE633470D patent/BE633470A/xx unknown
- NL NL293877D patent/NL293877A/xx unknown
- NL NL293837D patent/NL293837A/xx unknown
-
1962
- 1962-06-12 GB GB4297064A patent/GB1030746A/en not_active Expired
- 1962-06-12 GB GB2252362A patent/GB1030745A/en not_active Expired
- 1962-06-13 GB GB2270162A patent/GB1026802A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
NL293877A (en) | |
BE633469A (en) | |
GB1026802A (en) | 1966-04-20 |
BE633470A (en) | |
NL293837A (en) | |
GB1030745A (en) | 1966-05-25 |
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