Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Isoprene | HCID 6557 | — |
| Reactant | Heptane | HCID 8900 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Octane | HCID 356 | — |
| Product | Isoprene | HCID 6557 | — |
| Product | Dodecane | HCID 8182 | — |
Reaction Steps
The volatile hydrocarbon, e.g., isoprene, is harvested by passing the gaseous phase that contains the volatile hydrocarbon, e.g., isoprene, and O2 through a cooled condenser. The volatile hydrocarbon, e.g., isoprene, may then be collected. In some embodiments, the condensed hydrocarbon, e.g., condensed isoprene, is passed through a solvent, typically an organic solvent. Alcohols such as methanol (boiling point 64.7° C.), ethanol (boiling point 78.0° C.), butanol (boiling point 117.7° C.), and pure hydrocarbons such as hexane (boiling point 69.0° C.), heptane (boiling point 98.4° C.), octane (boiling point 125.5° C.), and dodecane (boiling point 216.2° C.) readily form stable “blends” with isoprene, or other volatile hydrocarbons obtained in accordance with the invention, thereby facilitating its retention and stabilization in a liquid solution. Concentrations of isoprene (or, e.g., alcohol, aldehyde, or other volatile hydrocarbon) collected in this manner vary between 1%, when a solvent is used to trap the isoprene, and 100% isoprene when no solvent is used, but a condenser-temperature low enough is employed to enable retention of isoprene in the liquid phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08993290B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-97ce1bad81ac44a0a2b3550346433484 |
|---|
| Source note | uspto-grants-2015_03 |
|---|