Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | Sodium vinylsulfonate | HCID 3270262 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Oxygen | HCID 977 | — |
| Product | Acrylamide | HCID 6579 | — |
| Product | Acrylonitrile | HCID 7855 | — |
| Product | Vinylsulfonic acid | HCID 62474 | — |
Reaction Steps
A water-soluble copolymer of acrylonitrile, acrylamide and ethylene sulfonic acid was prepared in the following way: 57.5 g of an aqueous 47% solution of sodium ethylene sulfonate, stabilized against polymerization by 0.2% sodium nitrite, was destabilized by adding 3 g urea and acidified with concentrated hydrochloric acid to pH 2. The developing gases were repeatedly drawn off. 7.1 g Acrylamide and 13.6 ml acrylonitrile were added and the monomer mixture was dissolved in 76 ml of oxygen-free water. 1 ml of a 5% sodium pyrosulfite solution and the same amount of ammonium persulfate were stirred in, and the somewhat turbid solution was left standing under carbon dioxide at room temperature for 24 hours. The viscous solution thus obtained was poured into 2 liters of anhydrous ethanol. The white coagulate was purified by dissolving it in water and again precipitating it in anhydrous ethanol, broken to small pieces and dried at 70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03953545 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-035102b7b2114125aea921d27431fc01 |
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| Source note | uspto-grants-1976_04 |
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