Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | Formaldehyde;phenol | HCID 172281 | — |
Reaction Steps
Phenol ( 1 mol) and 50% formalin (0.6 mol) were charged to a reaction vessel and the temperature maintained below 40° C. whilst sodium hydroxide (0.004 mol) was added. The temperature was then raised to 80° C. The temperature was maintained at 80° C. while a second charge of 50% formalin (1.0 mol) was added slowly over 30 minutes and the temperature maintained at 80° C. for a further 15 minutes. The mixture was then held at 70° C. for a further 30 minutes. The pH was adjusted with p-toluene sulphonic acid solution to 4.0 +/-0.2 and the volatiles distilled off under vacuum at 70° C. to a viscosity of 80 centistokes at 25° C. The resin was cooled to 60° C., the pH adjusted to 6.2 +/-0.02 with sodium hydroxide, 0.027 moles of urea were added and the product further concentrated to a final viscosity of 500 cP at 25° C., cooled and discharged.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05051454 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-492bec93932549deadc5497694d25ccc |
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| Source note | uspto-grants-1991_09 |
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