Isopropanol → Sodium styrene sulfonate styrene

HRID 2179838Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2179838
C(O)(C)C.[CH2:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH:13]([S:21]([O-:24])(=[O:23])=[O:22])=[CH:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[Na+:25].S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+]>O>[CH2:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH:13]([S:21]([O-:24])(=[O:22])=[O:23])=[CH:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[Na+:25]

Komponenten

6

Reaktionsbedingungen

Temperatur
83 °C

Versuchsvorschrift

A 1 L four-necked flask was charged with 91 g of isopropyl alcohol (manufactured by Kishida Chemical Co., Ltd.), 137 g of ion exchanged water, 10 g of styrene (manufactured by Kishida Chemical Co., Ltd.), and 40 g of sodium styrene sulfonate (manufactured by Wako Pure Chemical Industries, Ltd.), and the temperature was raised to 83±2° C. After introducing 6.6 g of ammonium persulfate (manufactured by Wako Pure Chemical Industries, Ltd.) as an initiator, the mixture was polymerized for two hours, and further aged for two hours. Thereafter, the solvent was removed under reduced pressure to give styrene/sodium styrene sulfonate copolymer (33/67 mol %). The weight-average molecular weight of this copolymer was 16000.

Aufarbeitung

  1. customthe mixture was polymerized for two hours
  2. customThereafter, the solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-f8a51ab3a63b48f3a4f06cb8685a8ceb
Quelldatensatz
uspto-grants-2015_06
Patentnummer
US09070399B2

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