HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 1,2-Diethenylbenzene--4-ethenylpyridine (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 4-Vinylpyridine | HCID 7502 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,2-Diethenylbenzene | HCID 66666 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,2-Diethenylbenzene--4-ethenylpyridine (1/1) | HCID 165743 | — |
Reaction Steps
One of the membranes thus obtained (C) was treated with an aqueous ethanol solution of NaOH to convert the --SO3H groups to their sodium salt form. The membrane (C) was then spread on one side with a mixture of the following molar composition: 90% of 4-vinylpyridine, 10% of divinylbenzene and 1% (by moles with respect to the total moles of monomers) dibenzoylperoxide and then was heated in a reactor at 80° C. for 3 hours to effect copolymerization to finally obtain an 0.05 mm thick 4-vinylpyridine/divinylbenzene copolymer layer on one side of the sulfonated membrane (C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04295952 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-fcf2320d08f1452faddbe56b039c16a4 |
| Source note | uspto-grants-1981_10 |