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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1050436Erstellt: 26. Oktober 2026

Hydroquinone → Acrylonitrile-butadiene mono-n-butyl maleate

https://huagongshe.com/reaction/1050436

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroquinoneHCID 785—
Edukt1,3-ButadieneHCID 7845—
EduktAcrylonitrileHCID 7855—
EduktCumen hydroperoxideHCID 53627471—
EduktSodium dodecylbenzene sulphonateHCID 57371080—
EduktMono-n-butyl maleateHCID 86595084—
LösungsmittelWaterHCID 962—
ProduktAcrylonitrile-butadiene mono-n-butyl maleateHCID 131729233—

Reaktionsschritte

To a metal bottle, ion exchanged water in 180 parts, concentration 10 wt % of sodium dodecyl benzene sulfonate aqueous solution in 25 parts, acrylonitrile in 37 parts, mono-n-butyl maleate in 6 parts, and t-dodecyl mercaptan (molecular weight adjuster) in 0.75 part were charged in that order. The inside air was replaced with nitrogen three times, then 1,3-butadiene in 57 parts was charged. The metal bottle was held at 5° C., cumen hydroperoxide (polymerization initiator) in 0.1 part was charged, then the metal bottle was rotated while performing a polymerization reaction for 16 hours. After that, a concentration 10 wt % of hydroquinone aqueous solution (polymerization anticatalyst) in 0.1 part was added to stop the polymerization reaction, then a water temperature 60° C. rotary evaporator was used to remove the residual monomers and thereby obtain a latex of acrylonitrile-butadiene-mono-n-butyl maleate copolymer rubber (solid concentration of about 30 wt %).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09382391B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-252119a7ca6e4b9d92dbfb63e714065f
Quellennotizuspto-grants-2016_07