Azobisisobutyronitrile → Styrenesulfonate perfluorooctene

HRID 254136Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 254136
[CH:1]([S:9]([O-:12])(=[O:11])=[O:10])=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[Na+].[F:14][C:15]([F:37])=[C:16]([F:36])[C:17]([F:35])([F:34])[C:18]([F:33])([F:32])[C:19]([F:31])([F:30])[C:20]([F:29])([F:28])[C:21]([F:27])([F:26])[C:22]([F:25])([F:24])[F:23].N(C(C)(C)C#N)=NC(C)(C)C#N>CS(C)=O>[CH:1]([S:9]([O-:12])(=[O:10])=[O:11])=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[F:14][C:15]([F:37])=[C:16]([F:36])[C:17]([F:34])([F:35])[C:18]([F:32])([F:33])[C:19]([F:30])([F:31])[C:20]([F:29])([F:28])[C:21]([F:27])([F:26])[C:22]([F:25])([F:24])[F:23]

Komponenten

5

Versuchsvorschrift

16 g of sodium styrenesulfonate (SSNa) (available from Sigma-Aldrich Corp.) and 4 g of perfluorooctene (1H,1H,2H-perfluoro-1-octene) are fully dissolved in 0.24 L of dimethylsulfoxide (DMSO) with heating. Then, 0.1 g of azobisisobutyronitrile (AIBN) is added dropwise to the DMSO solution. The monomers are polymerized for 24 hours or more. The polymerization is carried out varying the content of perfluorooctene (5, 10, and 20 wt %). The reaction product is allowed to sit at ambient temperature. Then, a precipitate is colleted from the reaction product and filtered with a filter to obtain a poly(styrenesulfonate-perfluorooctene) copolymer {P(SSNa-co-PFO)).

Aufarbeitung

  1. temperaturewith heating
  2. customThe monomers are polymerized for 24 hours or more
  3. customto sit at ambient temperature
  4. filtrationfiltered with
  5. filtrationa filter

Quellen und Nachweise

ORD-Eintrag
ord-0c8c1e0f5bec43adb00d0ea8fe72e99f
Quelldatensatz
uspto-grants-2011_01
Patentnummer
US07875208B2

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