HuagongsheHuagongshe Chemistry Print Report · For research reference only
Naphthalene → Phthalic Anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Phthalic Acid | HCID 1017 | — |
| Reactant | Succinic Acid | HCID 1110 | — |
| Reactant | 1,4-Naphthoquinone | HCID 8530 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Catalyst | HCID 178419084 | HCID 178419084 | — |
| Product | Phthalic Anhydride | HCID 6811 | 99% |
Reaction Steps
The optimum yield of phthalic anyhdride is produced in the temperature range of 360° ± 10° C, with temperatures over or under this range resulting in over or under oxidation, respectively, of the napthalene yielding undesirable products such as 1-4 napthoquinone, phthalic acid, maleic acid, succinic acid, etc. With a vanadium pentoxide catalyst structure made according to the present invention, a yield of 99% phthalic anhydride was obtained with only a slight trace of 1-4 napthoquinone. Throughout this reaction, the temperature of the catalyst structure was easily maintainable within the optimum operating temperature range of 360° C ± 10° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062872 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-9c7841d5250b4b158d7b59a13727c286 |
| Source note | uspto-grants-1977_12 |