Reaktionsgleichung
[C:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH:11]([CH3:13])[CH3:12])(=[O:4])[CH:2]=[CH2:3].[C:14]([NH2:18])(=[O:17])[CH:15]=[CH2:16].[C:19]([O:22][CH:23]=[CH2:24])(=[O:21])[CH3:20].N(C(C)(CC(C)C)C#N)=NC(C)(CC(C)C)C#N>C(OCC)(=O)C.CO>[C:1]([O:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH:11]([CH3:13])[CH3:12])(=[O:4])[CH:2]=[CH2:3].[C:14]([NH2:18])(=[O:17])[CH:15]=[CH2:16].[C:19]([O:22][CH:23]=[CH2:24])(=[O:21])[CH3:20]Komponenten
Versuchsvorschrift
A master batch was prepared by combining isooctyl acrylate (62 1.0 g), acrylamide (41.4 g), vinyl acetate (165.6 g), 2,2' azobis (2,4-dimethylpentanenitrile) (1,656 g, VAZO™ 52, DuPont), ethyl acetate (884.5 g) and methanol (87.48 g). A portion (400 g) of the resulting solution was placed in a one quart (0.95 liter) amber glass bottle. The bottle was purged for 2 minutes with nitrogen at a flow rate of 1 liter per minute. The bottle was sealed and placed in a rotating water bath at 45° C. for 24 hours to effect essentially complete polymerization. The copolymer was diluted with ethyl acetate: methanol (250 g, 90:10 volume-to-volume) to 26.05% solids and had a measured inherent viscosity of 1.27 deciliter/g in ethyl acetate at a concentration of 0.15 g/deciliter.
Aufarbeitung
- customA master batch was prepared
- customThe bottle was purged for 2 minutes with nitrogen at a flow rate of 1 liter per minute
- customThe bottle was sealed
- custompolymerization
Quellen und Nachweise
- ORD-Eintrag
- ord-d3b51a95eec04b29a244d6e624415c12
- Quelldatensatz
- uspto-grants-1996_12
- Patentnummer
- US05585111
Verknüpfte Notizen
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