HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Terephthalic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | Mycophenolic acid glucuronide | HCID 6442661 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Catalyst | Manganous Acetate | HCID 12525 | — |
| Product | Terephthalic Acid | HCID 7489 | — |
Reaction Steps
An example of the liquid-phase oxidation reaction is as follows. For example, using an apparatus with a commercial scale, p-xylene is subjected to liquid-phase oxidation by air (reaction temperature: 200 [° C.]; reaction pressure: 1.5 [MPaG]) in the presence of cobalt acetate, manganese acetate and hydrobromic acid in hydrous acetic acid to obtain a crude terephthalic acid slurry (the concentration of terephthalic acid: 34% by weight; the concentration of water in the hydrous acetic acid that is a dispersing medium: 11% by weight), and the resulting slurry is then introduced into crystallization vessels connected in series to subject the slurry to sequential pressure drop.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150487B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-fe7bfc5d424a4c548b99b5941b2318aa |
| Source note | uspto-grants-2015_10 |