Deactivation of a process by-product
US-9505675-B2 · Nov 29, 2016 · US
US9802874B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9802874-B2 |
| Application number | US-201314086530-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 21, 2013 |
| Priority date | Jan 18, 2007 |
| Publication date | Oct 31, 2017 |
| Grant date | Oct 31, 2017 |
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Disclosed herein is a method of preparing 1-octene at high activity and high selectivity while stably maintaining reaction activity by tetramerizing ethylene using a chromium-based catalyst system comprising a transition metal or a transition metal precursor, a cocatalyst, and a P—C—C—P backbone structure ligand represented by (R 1 )(R 2 )P—(R 5 )CHCH(R 6 )—P(R 3 )(R 4 ).
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The invention claimed is: 1. A method of preparing 1-octene by tetramizing ethylene using the following catalyst system consisting essentially of : chromium or chromium compound, an alkylaluminoxane cocatalyst, and a P—C—C—P backbone structure ligand represented by Formula 1 below: wherein R1, R2, R3 and R4 are each independently a hydrocarbyl group, a substituted hydrocarbyl group, a heterohydrocarbyl group and a substituted heterohydrocarbyl group, and each of the R1, R2, R3 and R4 has no substituent on atoms adjacent to the atoms bonded with P atoms. 2. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the method is operated at a temperature of −20-250° C. 3. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the method is operated at a temperature of 15-130° C. 4. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the method is operated at a temperature of 30-70° C. 5. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the method is operated at a pressure of atmospheric pressure-500 bar. 6. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the method is operated at a pressure of 10-70 bar. 7. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the method is operated at a pressure of 30-50 bar. 8. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the method is operated using inactive solvent selected from saturated aliphatic hydrocarbons, unsaturated aliphatic hydrocarbons, aromatic hydrocarbons, halogenated hydrocarbons, or a combination thereof. 9. The method of preparing 1-octene by tetramizing ethylene of claim 8 , wherein the inactive solvent selected from benzene, toluene, xylene, cumene, heptanes, cyclohexane, methylcyclohexane, methylcyclopentane, n-hexane, 1-hexene or a combination thereof. 10. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the aluminum of alkylaluminoxane : chromium or chromium compound is 1:1-10,000:1. 11. The method of preparing 1-octene by tetramizing ethylene of claim 1 , wherein the aluminum among alkylaluminoxane : chromium or chromium compound is 1:1-1,000:1.
Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring · CPC title
Metal-hydrocarbon complexes · CPC title
with more than one complexing phosphine-P atom · CPC title
Alkenes · CPC title
with hydrides or organic compounds (C07C2/20 takes precedence) · CPC title
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