HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → Terephthalic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 1,4-Benzenedicarboxylate | HCID 154269 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Water | HCID 962 | — |
| Product | Terephthalic Acid | HCID 7489 | — |
Reaction Steps
0.22 grams of a potassium salt of terephthalate was dissolved in 10.5 grams of deionized water in a 20 ml vial, and 5 grams of dry ice was added directly, and the vial was loosely capped. After two to three minutes, the solution became cloudy, and soon a large quantity of flocculent terephthalic acid precipitate was formed. After filtration, about 40% of the theoretical yield of terephthalic acid was recovered. The filtrate was a clear solution of potassium salts. The pH increased from about 6 when chilled before filtration to about 7 after the dry ice had all sublimed, and the solution warmed to room temperature, showing the presence of excess base after the CO2 had outgassed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441225B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-91b36edb33b34c779ed6436d6740fe4b |
| Source note | uspto-grants-2002_08 |