Reaktionsgleichung
S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+].C(OC=C)(=O)C.[C:19]([O:34][CH2:35][CH2:36][CH2:37]C)(=[O:33])[C:20]1[C:21](=[CH:29][CH:30]=[CH:31][CH:32]=1)[C:22]([O:24][CH2:25][CH2:26][CH2:27]C)=[O:23]>O>[C:22]([O:24][CH2:25][CH:26]=[CH2:27])(=[O:23])[C:21]1[C:20](=[CH:32][CH:31]=[CH:30][CH:29]=1)[C:19]([O:34][CH2:35][CH:36]=[CH2:37])=[O:33]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
0.2 g of defoamer and 12 g of Fixapret COC were added to and mixed with a solution of 47 g of polyvinyl alcohol in 600 g of water. The mixture was heated to about 80° C. About 90% of a catalyst solution of 1.3 g of ammonium persulfate in 6 g of water were then added and the mixture was homogenized for about 5 minutes. A mixture of 460 g of vinyl acetate and 10 g of dibutyl phthalate was then added over a period of about 3.5 to 4 hours so that the temperature stayed between 82 and 88° C. After the monomer mixture had been added, the remaining catalyst solution was added and the reaction mixture was stirred for about 1 hour at a temperature of about 90° C. The solids content was then adjusted to about 55%. After the dispersion had cooled to a temperature of about 35 to about 40° C., 15 g of dibutyl phthalate were added. The product thus obtained had a pH of 4.2 and a viscosity (5/2120) of 44,000 cps.
Aufarbeitung
- addition0.2 g of defoamer and 12 g of Fixapret COC were added to and
- additionwas then added over a period of about 3.5 to 4 hours so that the temperature
- customstayed between 82 and 88° C
- additionAfter the monomer mixture had been added
- additionthe remaining catalyst solution was added
- stirringthe reaction mixture was stirred for about 1 hour at a temperature of about 90° C
- additionwere added
- customThe product thus obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-53ea9cf14a8744f78909ae696f4bfac7
- Quelldatensatz
- uspto-grants-2006_07
- Patentnummer
- US07078448B2
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