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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2188499Erstellt: 25. Oktober 2026

Nitrogen → N,N-Dimethylacrylamide 2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium Salt

https://huagongshe.com/reaction/2188499

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktSodium HydroxideHCID 14798—
EduktSenecioic acid amideHCID 20560—
EduktAmmonium PersulfateHCID 62648—
Edukt2-Acrylamido-2-methyl-1-propanesulfonic acidHCID 65360—
EduktEmulphorHCID 5364713—
EduktMethylene-bisacrylamideHCID 53800990—
EduktHCID 178435162HCID 178435162—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
ProduktN,N-Dimethylacrylamide 2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium SaltHCID 87703436—

Reaktionsschritte

Firstly, 35 g of dimethylacrylamide (manufactured by Kojin Co., Ltd.), 17.5 g of 2-acrylamido-2-methylpropanesulfonic acid (manufactured by Sigma), and 7 mg of methylenebisacrylamide were dissolved in ion-exchanged water, and the pH value of the resulting solution was adjusted at 7.0 by the addition of sodium hydroxide. Thereafter, 260 g of n-hexane, 8.7 g of polyoxyethylene (3) oleyl ether (EMULEX 503, manufactured by Nihon Emulsion Co., Ltd.), and 17.6 g of polyoxyethylene (6) oleyl ether (EMULEX 506, manufactured by Nihon Emulsion Co., Ltd.) were introduced into a 1,000 ml three-neck flask provided with a reflux device, were mixed together, and were thus subjected to dissolution. The inside atmosphere of the three-neck flask was then replaced by an N2 gas. The aqueous monomer solution having been prepared in the manner described above was then introduced into the three-neck flask. The resulting mixture was heated to a temperature of 65° C. to 70° C. in an oil bath, while the mixture was being stirred under the N2 gas atmosphere. At the stage at which the system had reached the temperature of 65° C. to 70° C., it was confirmed that the system had come into a semitransparent microemulsion state, and 2 g of ammonium persulfate was then added to the polymerization system. Polymerization was thus begun. The polymerization system was kept at the temperature of 65° C. to 70° C. with stirring, and a microgel was thus formed. After the polymerization had finished, acetone was added to the microgel suspension, and the microgel was thus precipitated. Subsequently, washing with acetone was performed three times, and the residual monomers and the surfactants were thus removed. The obtained precipitate was collected by filtration and dried under reduced pressure, and a white powder-like microgel dry product was thereby obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08323629B2
Quelldatensatzuspto-grants-2012_12
ORD IDord-aa1b19d1538645b3bddf7cf3837b6d6d
Quellennotizuspto-grants-2012_12