戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1835898作成日:2026年10月26日

Vinylidene fluoride → Pmve tfe 2-hpfp

https://huagongshe.com/reaction/1835898

反応式

関与物質

役割名称HCID仕込み量
反応物Vinylidene fluorideHCID 6369—
反応物TetrafluoroethyleneHCID 8301—
反応物Sodium HydroxideHCID 14798—
反応物Ammonium PersulfateHCID 62648—
反応物1,1,3,3,3-PentafluoropropeneHCID 69647—
反応物1,2,3,3,3-Pentafluoro-1-[(1,2,3,3,3-pentafluoroprop-1-en-1-yl)oxy]prop-1-eneHCID 57349567—
溶媒WaterHCID 962—
溶媒IsopropanolHCID 3776—
生成物Pmve tfe 2-hpfpHCID 131724522—

反応手順

A VF2/PMVE/TFE/2-HPFP fluoroelastomer was prepared by a continuous emulsion polymerization process of the invention in a well-stirred 4.0-liter stainless steel liquid full reaction vessel at 110° C. An aqueous solution, consisting of 3.5 g/hour (g/h) ammonium persulfate, 2.0 g/h sodium hydroxide, 8.4 g/h Zonyl® FS-62 fluorosurfactant (25 wt. % A.I.) solution, and 2.4 g/h isopropanol in deionized water, was fed to the reactor at a rate of 8 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 185 g/h tetrafluoroethylene (TFE), 1237 g/h vinylidene fluoride (VF2), and 835 g/h perfluoro(methyl vinyl) ether (PMVE) fed through a diaphragm compressor. After 15 minutes more, 2-hydropentafluoropropylene (2-HPFP) was introduced into the remainder of the gaseous mixture and added at a rate of 68.5 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 5.23 and contained 22.6 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 twice 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 14 kg of fluoroelastomer was recovered at an overall conversion of 97.1%. The product, containing 8.2 wt. % TFE units, 54.1 wt. % VF2 units, 35.9 wt. % PMVE units and 1.84 wt. % 2-HPFP units, was an amorphous elastomer having a glass transition temperature of −30° C., as determined by DSC (heating mode, 10° C./minute, inflection point of transition). Inherent viscosity of the elastomer was 0.89 dL/g, measured at 30° C. in methyl ethyl ketone, and Mooney viscosity, ML (1+10), was 53.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06774164B2
出典データセットuspto-grants-2004_08
ORD IDord-9cf108fe5d3a4622809698b1c4bcd995
出典メモuspto-grants-2004_08