Vinylidene fluoride → Pmve tfe btfb

A VF2/PMVE/TFE/BTFB fluoroelastomer was prepared by a continuous emulsion polymerization of the invention in a well-stirred 4.0-liter stainless steel liquid full reaction vessel at 110° C. An aqueous solution, consisting of 10.32 g/hour (g/h) ammonium persulfate, 4.53 g/h sodium hydroxide, and 8.9 g/h Zonyl® FS-62 fluorosurfactant (25 wt. % A.I) solution in deionized water, was fed to the reactor at a rate of 10 L/hour. The reactor was maintained at a liquid-full level at a pressure of 6.2 MPa by means of a back-pressure control valve in the effluent line. After 30 minutes, polymerization was initiated by introduction of a gaseous monomer mixture consisting of 667 g/h tetrafluoroethylene (TFE), 872 g/h vinylidene fluoride (VF2), and 1138 g/h perfluoro(methyl vinyl) ether (PMVE) fed through a diaphragm compressor. After 15 minutes more, 4-bromo-3,3,4,4-tetrafluorobutene-1 (BTFB) added at a rate of 40.0 g/h. After 2.0 hours, collection of the resulting fluoroelastomer latex was begun and continued for 6 hours. The latex, which had a pH of 3.87 and contained 20.7 wt. % solids, was separated from residual monomers in a degassing vessel at atmospheric pressure. Fluoroelastomer crumb product was isolated from the latex by reducing the pH to about 3 with dilute sulfuric and coagulating with aluminum sulfate solution. The coagulated fluoroelastomer polymer was allowed to settle, supernatant serum was removed, and the polymer was washed by reslurrying in water three times before filtering. The wet crumb was dried in an air oven at approximately 50°-65° C. to a moisture content of less than 1 wt. %. About 15 kg of fluoroelastomer was recovered at an overall conversion of 96.0%. The product, containing 25.3 wt. % TFE units, 33.1 wt. % VF2 units, 40.0 wt. % PMVE units and 1.54 wt. % BTFB units, was an amorphous elastomer having a glass transition temperature of −22° C., as determined by DSC (heating mode, 10° C./minute, inflection point of transition). Inherent viscosity of the elastomer was 0.66 dL/g, measured at 30° C. in methyl ethyl ketone, and Mooney viscosity, ML (1+10), was 77.

1. temperatureThe reactor was maintained at a liquid-full level at a pressure of 6.2 MPa by means of a back-pressure control valve in the effluent line
2. custompolymerization
3. waitAfter 15 minutes more
4. waitAfter 2.0 hours
5. customcollection of the resulting fluoroelastomer
6. waitcontinued for 6 hours
7. customwas separated from residual monomers in a degassing vessel at atmospheric pressure

ORD 기록

ord-436dbf233cb84dcc85c00b3246322be9

출처 데이터셋

uspto-grants-2004_08

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US06774164B2