Acrylamide → N-Octylacrylamide Acrylamide Sodium Styrene Sulfonate
反応式
[CH2:1]([NH:9][C:10](=[O:13])[CH:11]=[CH2:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[C:14]([NH2:18])(=[O:17])[CH:15]=[CH2:16].[CH:19]([S:27]([O-:30])(=[O:29])=[O:28])=[CH:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[Na+:31]>CO>[CH2:1]([NH:9][C:10](=[O:13])[CH:11]=[CH2:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[C:14]([NH2:18])(=[O:17])[CH:15]=[CH2:16].[CH:19]([S:27]([O-:30])(=[O:28])=[O:29])=[CH:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[Na+:31]参加物
反応条件
- 温度
- 25 °C
実験手順
A solution of 15.0 g of SDS in 500 ml of purified, deoxygenated water was prepared and 0.415 g of N-octylacrylamide, 12.73 g of acrylamide and 9.35 g of sodium styrene sulfonate were added. The resulting clear solution was placed in a 2 liter Morton style resin kettle fitted with a chilled water condenser, thermometer, nitrogen sparger and mechanical stirrer. The solution was purged with nitrogen for 0.5 hour at 25° C., then 0.116 g of potassium persulfate and 0.0082 g of sodium metabisulfite were added. After 16 hours of stirring at 300 rpm and 25° C. the reaction mixture was slowly poured into 3 L of acetone. The precipitated polymer was isolated and masticated with 1 L of methanol in a Waring blender for 30 seconds, filtered and dried under vacuum at 30° C. The yield of polymer was 5.14 g.
後処理
- customA solution of 15.0 g of SDS in 500 ml of purified
- customdeoxygenated water
- customwas prepared
- customfitted with a chilled water condenser
- customThe solution was purged with nitrogen for 0.5 hour at 25° C.
- addition0.116 g of potassium persulfate and 0.0082 g of sodium metabisulfite were added
- additionwas slowly poured into 3 L of acetone
- customThe precipitated polymer was isolated
- filtrationfiltered
- customdried under vacuum at 30° C
出典と根拠
- ORDレコード
- ord-1f131f8a52a5430b8710219ac2ce5ea1
- 出典データセット
- uspto-grants-1988_03
- 特許番号
- US04730028
反応ノート
読み込み中…