GB1284459A - Fluorinated elastomer admixture, process for its curing and resulting cured elastomeric product - Google Patents
Fluorinated elastomer admixture, process for its curing and resulting cured elastomeric productInfo
- Publication number
- GB1284459A GB1284459A GB4119069A GB4119069A GB1284459A GB 1284459 A GB1284459 A GB 1284459A GB 4119069 A GB4119069 A GB 4119069A GB 4119069 A GB4119069 A GB 4119069A GB 1284459 A GB1284459 A GB 1284459A
- Authority
- GB
- United Kingdom
- Prior art keywords
- quaternary ammonium
- compound
- radical
- vinylidene fluoride
- curing
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/19—Quaternary ammonium compounds
Abstract
1284459 Curing vinylidene fluoride copolymers MINNESOTA MINING & MFG CO 18 Aug 1969 [19 Aug 1968 27 Feb 1969 9 June 1969] 41190/69 Heading C3P A composition capable of being cured in the presence of an oxidizable aromatic hydroxy or amino compound and an inorganic acid acceptor capable of generating water upon reaction with hydrogen fluoride, comprises an elastomeric copolymer of vinylidene fluoride and at least one terminally unsaturated fluoro-monolefin in which at least 10% of the chain carbon atoms of the copolymer are in the form of -CH 2 - units, at least one quaternary ammonium hydroxide or a quaternary ammonium salt which is capable under the conditions of cure of forming a quaternary ammonium hydroxide and at least one compound which is stable in the absence of water at temperatures below 75‹ C., and which at a temperature above 125‹ C. and in the presence of water releases a basic nitrogen atom containing compound having at least one hydrogen atom bonded to the basic nitrogen atom. The compositions are cured in the presence of the aromatic compound and the acid acceptor in a mould at a pressure of between 7 and 210 kg./cm.<SP>2</SP> at a temperature of between 95‹ and 230‹ C. for a period of between 1 minute and 15 hours. Suitable copolymers are those of vinylidene fluoride with chlorotrifluoroethylene, perfluoropropene, 1-hydroperfluoropropene and/or tetrafluoroethylene. Suitable quaternary ammonium hydroxides are those of formula [R<SP>1</SP> 3 -NR<SP>2</SP>-N-R<SP>3</SP> 3 ]<SP>++</SP>[OH<SP>-</SP>] 2 or [R<SP>4</SP>-N-R<SP>5</SP> 3 ]<SP>+</SP>OH<SP>-</SP> in which R<SP>1</SP>, R<SP>3</SP> and R<SP>5</SP> represent C 1-18 alkyl radicals, R<SP>2</SP> represents a C 2-12 alkylene radical or a C 8-12 phenylene dialkylene radical, R<SP>4</SP> is a C 1-12 alkyl radical or a C 7-12 aralkyl radical. Suitable quaternary ammonium salts are alkoxides, phenoxides and acetates. Suitable acid acceptors are magnesium oxide, lead oxide, zinc oxide and dibasic lead phosphite The preferred aromatic compound is hydro. quinone. An inorganic base may also be included.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US75361868A | 1968-08-19 | 1968-08-19 | |
US80291769A | 1969-02-27 | 1969-02-27 | |
US83129569A | 1969-06-09 | 1969-06-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1284459A true GB1284459A (en) | 1972-08-09 |
Family
ID=27419450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4119069A Expired GB1284459A (en) | 1968-08-19 | 1969-08-18 | Fluorinated elastomer admixture, process for its curing and resulting cured elastomeric product |
Country Status (7)
Country | Link |
---|---|
BE (1) | BE737616A (en) |
CH (1) | CH525917A (en) |
ES (1) | ES370597A1 (en) |
FR (1) | FR2017167A1 (en) |
GB (1) | GB1284459A (en) |
NL (1) | NL6912561A (en) |
SE (1) | SE360877B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4353961A (en) | 1977-09-14 | 1982-10-12 | Raychem Corporation | Shaped article from crosslinked fluorocarbon polymer |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH05339536A (en) * | 1992-06-11 | 1993-12-21 | Minnesota Mining & Mfg Co <3M> | Fluorinated rubber composition for coating |
-
1969
- 1969-08-18 GB GB4119069A patent/GB1284459A/en not_active Expired
- 1969-08-18 FR FR6928183A patent/FR2017167A1/fr active Pending
- 1969-08-18 ES ES370597A patent/ES370597A1/en not_active Expired
- 1969-08-18 CH CH1249769A patent/CH525917A/en not_active IP Right Cessation
- 1969-08-18 BE BE737616D patent/BE737616A/xx not_active IP Right Cessation
- 1969-08-18 NL NL6912561A patent/NL6912561A/xx unknown
- 1969-08-18 SE SE1147169A patent/SE360877B/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4353961A (en) | 1977-09-14 | 1982-10-12 | Raychem Corporation | Shaped article from crosslinked fluorocarbon polymer |
Also Published As
Publication number | Publication date |
---|---|
NL6912561A (en) | 1970-02-23 |
CH525917A (en) | 1972-07-31 |
FR2017167A1 (en) | 1970-05-22 |
DE1941915A1 (en) | 1970-02-26 |
DE1941915B2 (en) | 1972-02-24 |
SE360877B (en) | 1973-10-08 |
ES370597A1 (en) | 1971-08-01 |
BE737616A (en) | 1970-02-18 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PE20 | Patent expired after termination of 20 years |