HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1050436Erstellt: 26. Oktober 2026
Hydroquinone → Acrylonitrile-butadiene mono-n-butyl maleate
https://huagongshe.com/reaction/1050436
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydroquinone | HCID 785 | — |
| Edukt | 1,3-Butadiene | HCID 7845 | — |
| Edukt | Acrylonitrile | HCID 7855 | — |
| Edukt | Cumen hydroperoxide | HCID 53627471 | — |
| Edukt | Sodium dodecylbenzene sulphonate | HCID 57371080 | — |
| Edukt | Mono-n-butyl maleate | HCID 86595084 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Acrylonitrile-butadiene mono-n-butyl maleate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09382391B2 |
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| Quelldatensatz | uspto-grants-2016_07 |
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| ORD ID | ord-252119a7ca6e4b9d92dbfb63e714065f |
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| Quellennotiz | uspto-grants-2016_07 |
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