Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 568862Erstellt: 24. Oktober 2026

Acrylamide → N-Octylacrylamide Acrylamide Vinyl Sulfonate

https://huagongshe.com/de/reaction/568862

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcrylamideHCID 6579—
EduktPotassium PersulfateHCID 24412—
Edukt2-Propenamide, N-octyl-HCID 82370—
EduktSodium vinylsulfonateHCID 3270262—
EduktSodium Lauryl SulfateHCID 3423265—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktN-Octylacrylamide Acrylamide Vinyl SulfonateHCID 86742029—

Reaktionsschritte

A one liter Morton style resin kettle, fitted with a chilled water condenser, thermometer, nitrogen sparger and mechanical stirrer was charged with 500 ml of purified water. The water was refluxed for 1 hour with a nitrogen purge and then cooled to room temperature. Acrylamide, 9.886 g (0.14 mole), 4.81 g (0.37 mole) of sodium vinyl sulfonate as a 25% solution in water, 0.33 g (0.002 mole) of N-octylacrylamide and 15 g of sodium dodecyl sulfate (SDS) were charged into the flask. The reaction solution was heated to 50° C. and 0.01 g potassium persulfate was added. After 17 hours at 50° C. and 300 rpm stirring, the viscous solution was slowly poured into 3 L of methanol and the precipitated polymer was isolated by filtration. The polymer was then masticated in a Waring blender with 2 L of methanol for 30 seconds, filtered and dried under vacuum at room temperature. The yield of the polymer was 10.9 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04730028
Quelldatensatzuspto-grants-1988_03
ORD IDord-bd2c09e4fa2941e1be28610657c18648
Quellennotizuspto-grants-1988_03