Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | P-Phenylenediamine | HCID 7814 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Product | Nitric Acid | HCID 944 | — |
| Product | Ammonium nitrate | HCID 22985 | — |
| Product | Hydroxylamine nitrate | HCID 26045 | — |
Reaction Steps
The general procedure of Example 8 is repeated except that tetrabutylammonium chloride is added into the catholyte compartment. A solution of 1 M nitric acid, 50 mM 1,4-phenylenediamine and 0.1 M tetrabutylammonium chloride is charged to the catholyte compartment. A solution of 4 M nitric acid is charged to the anolyte compartment. Nitric acid is added to the catholyte compartment to maintain the nitric acid concentration between 0.5 M and 1 M under application of an electrical current. While maintaining the temperature between 5° C. and 10° C., a current of 45 amps (3 ASI) and a cell voltage of about 6.5 volts is applied. The catholyte is stirred under application of the current. A solution of 1.65 M hydroxylammonium nitrate and 0.7 M nitric acid with no detectable ammonium nitrate is obtained from the catholyte compartment. An overall current efficiency of 85% for formation of hydroxylammonium nitrate is achieved.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06024855 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-e0673ea4cd8f4e5b9a00dafe4d6d7caa |
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| Source note | uspto-grants-2000_02 |
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