HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methylhydroquinone → Sodium Chloride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methylhydroquinone | HCID 7253 | — |
| Edukt | 1,2-Diethenylbenzene | HCID 66666 | — |
| Edukt | Lithium Chloride | HCID 433294 | — |
| Edukt | Sodium styrenesulfonate | HCID 53627496 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | Sodium Chloride | HCID 5234 | — |
| Produkt | Lithium styrene sulfonate | HCID 86583601 | — |
Reaktionsschritte
In a 500 ml flat bottomed flask, 50 ml (52.2 g) N-methylpyrrolidone and 50 ml divinyl benzene (80%) are combined at a temperature of 70° C. with stirring. Ten grams of LiCl and 80 mg methylhydroquinone are added to the solution. Subsequently, 50 g sodium styrene sulfonate (81%) are added to the solution forming a suspension, and the reaction allowed to proceed at 70-80° C. for one hour. The LiCl reacts with the suspended sodium styrene sulfonate to form lithium styrene sulfonate and insoluble NaCl. The reaction mixture is allowed to cool to room temperature, and insoluble materials (NaCl and unreacted insoluble sodium styrene sulfonate) are removed by filtration. A brown, clear filtrate (121 g) is obtained for use in membrane synthesis.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06344584B1 |
| Quelldatensatz | uspto-grants-2002_02 |
| ORD ID | ord-1d5d34e378aa4bcd9c29d7c391449793 |
| Quellennotiz | uspto-grants-2002_02 |