Hydrogen-assisted adsorption of sulphur compounds from olefin mixtures
US-10370311-B2 · Aug 6, 2019 · US
US11325874B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11325874-B2 |
| Application number | US-201917263194-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 11, 2019 |
| Priority date | Jul 26, 2018 |
| Publication date | May 10, 2022 |
| Grant date | May 10, 2022 |
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Provided is a method for preparing a linear alpha olefin using a chromium-based catalyst, including the steps of: removing oxygen impurities by contacting an olefin with an oxygen adsorbent; injecting the olefin from which the oxygen impurities are removed; a chromium-based catalyst into a reactor; and oligomerizing the olefin in the reactor.
Opening claim text (preview).
The invention claimed is: 1. A method for preparing a linear alpha olefin, the method comprising steps of: removing oxygen impurities by contacting an olefin with an oxygen adsorbent; injecting the olefin from which the oxygen impurities are removed, and a chromium-based catalyst into a reactor; oligomerizing the olefin in the reactor; and terminating the oligomerizing reaction by using a catalyst deactivator, wherein the step of removing the oxygen impurities is performed under a temperature of 50 to 100° C. 2. The method of claim 1 , wherein the oxygen adsorbent is CuO, NiO, MoO 3 , zeolite 3A, activated alumina, or a mixture thereof. 3. The method of claim 1 , wherein the oxygen adsorbent has a specific surface area of 100 to 900 m 2 /g. 4. The method of claim 1 , wherein the step of removing the oxygen impurities is performed by passing the olefin through an adsorption tower filled with the oxygen adsorbent. 5. The method of claim 4 , wherein the olefin is injected into the adsorption tower at a gas hourly space velocity of 0.02 to 5 hr −1 . 6. The method of claim 4 , further comprising, after the step of removing the oxygen impurities, a step of regenerating the oxygen adsorbent. 7. The method of claim 6 , wherein the oxygen adsorbent is CuO, and the step of regenerating the oxygen adsorbent is performed by passing a mixed gas of hydrogen and nitrogen through the adsorption tower at 100 to 200° C. 8. The method of claim 7 , wherein a volume ratio of hydrogen and nitrogen in the mixed gas is 5:95 to 95:5. 9. The method of claim 1 , wherein the step of removing the oxygen impurities is performed under a pressure of 5 to 100 kg/cm 2 . 10. The method of claim 1 , wherein after the step of removing the oxygen impurities, an oxygen content in the olefin is less than 100 ppm. 11. The method of claim 10 , wherein the oxygen content in the olefin is 0 ppm. 12. The method of claim 1 , wherein the chromium-based catalyst is represented by CrL 1 (l 2 ) p (X) q or Cr 2 X 1 2 L 1 2 (L 2 ) y (X) z (where L 1 is a heteroligand, L 2 is an organic ligand, X and X 1 are each independently halogen, p is 0 or an integer of 1 or more, q is an integer of (oxidation number of Cr−p), y is an integer of 2 or more, and z is an integer of (2×oxidation number of Cr)−y). 13. The method of claim 1 , wherein the olefin is ethylene. 14. The method of claim 1 , wherein the catalyst deactivator is an oxygen-containing inorganic material selected from the group consisting of O 2 , CO 2 , CO, NO, NO 2 , N 2 O, N 2 O 3 , N 2 O 4 , N 2 O 5 and a mixture thereof; an organic compound including one or more of functional groups including at least one selected from the group consisting of oxygen, phosphorus, nitrogen and sulfur, and having a number average molecular weight of 400 or more; or 2-ethylhexanol. 15. The method of claim 14 , wherein the catalyst deactivator is an oxygen-containing inorganic material selected from the group consisting of O 2 , CO 2 , CO, NO, NO 2 , N 2 O, N 2 O 3 , N 2 O 4 , N 2 O 5 and a mixture thereof; or an organic compound including one or more of functional groups including at least one selected from the group consisting of oxygen, phosphorus, nitrogen and sulfur, and having a number average molecular weight of 400 or more.
by molecular-sieve technique · CPC title
containing metal-to-carbon bond; Metal hydrides · CPC title
using catalysts, e.g. selective catalysts · CPC title
as phosphines, arsines, stilbines or bismuthines · CPC title
of aluminium or boron · CPC title
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