Hydroformylation process
US-9174907-B2 · Nov 3, 2015 · US
US10131608B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10131608-B2 |
| Application number | US-201515114191-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 10, 2015 |
| Priority date | Mar 31, 2014 |
| Publication date | Nov 20, 2018 |
| Grant date | Nov 20, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A hydroformylation process wherein a water-soluble amine is contacted with the reaction fluid, liquid from the reactor is sent to an extraction zone, and a neutralized phosphorus acidic compound is at least partially removed from the extraction zone.
Opening claim text (preview).
What is claimed is: 1. A process comprising: (1) conducting in a reaction zone a hydroformylation reaction employing a reaction fluid comprising (a) a phosphorus acidic compound, (b) a metal-organophosphorus ligand complex catalyst that comprises a metal of Group 8, 9 or 10 complexed with an organophosphorous ligand, and, optionally, (c) free organophosphorus ligand; (2) contacting at least a portion of the reaction fluid with a water-soluble amine to neutralize at least some amount of the phosphorus acidic compound and to form a neutralized phosphorus acidic compound; (3) at least partially separating in an extraction zone at least one neutralized phosphorus acidic compound from the reaction fluid; and (4) removing the neutralized phosphorus acidic compound from the extraction zone via an extraction zone aqueous effluent stream; with the proviso that the amount of amine is such that the concentration of the amine in the reaction zone is not more than 0.075 mmoles per liter of hydroformylation reaction fluid. 2. The process of claim 1 wherein the concentration of the amine in the reaction zone is a positive amount that is not more than 0.05 mmole/liter of hydroformylation reaction fluid. 3. The process of claim 1 wherein the water solubility of the amine is at least 2:1, and the basicity of the amine, determined as the pKa of the conjugate acid, is from 5 to 11 at the temperature of the extraction. 4. The process of claim 1 wherein the water solubility of the amine is at least 100:1, and the basicity of the amine, determined as the pKa of the conjugate acid, is from 6.0 to 9.5 at the temperature of the extraction. 5. The process of claim 1 wherein the water solubility of the amine is at least 200:1, and the basicity of the amine, determined as the pKa of the conjugate acid, is from 6.5 to 9.0 at the temperature of the extraction. 6. The process of claim 1 wherein the amine comprises at least one of triethanolamine, methyldiethanolamine, ethyldiethanolamine, tri(2-hydroxypropyl)amine, and ethoxylates of these. 7. The process of claim 1 wherein the amine is triethanolamine. 8. The process of claim 1 wherein the extraction zone aqueous effluent stream has a pH of from 4.5 to 9. 9. The process of claim 1 wherein the extraction zone aqueous effluent stream has a pH of from 6.0 to 7.5. 10. The process of claim 1 wherein at least a portion of the water-soluble amine is added to the reaction zone, and the pH of the extraction zone aqueous effluent stream is controlled by controlling the rate of addition of the water-soluble amine to the reaction zone. 11. The process of claim 9 wherein at least a portion of the water-soluble amine is added to the extraction zone, and the pH of the extraction zone aqueous effluent stream is controlled by controlling the rate of addition of the water-soluble amine to the extraction zone.
Recycling of unreacted starting or intermediate materials · CPC title
Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts (catalysts comprising molecular sieves B01J29/00) · CPC title
by liquid-liquid treatment · CPC title
by oxo-reactions · CPC title
Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.