Salts of 5-[(1r)-2-(amino)-1-hydroxyethyl]-8-hydroxyquinolin-2(1h)-one
US-2015065471-A1 · Mar 5, 2015 · US
US10227271B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10227271-B2 |
| Application number | US-201615561381-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 7, 2016 |
| Priority date | Mar 30, 2015 |
| Publication date | Mar 12, 2019 |
| Grant date | Mar 12, 2019 |
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An integrated process, suitable for use in a new or retrofitted plant, produces an olefin or di-olefin via the dehydrogenation of an appropriate C3-C4 hydrocarbon feed includes (1) contacting the feed and a dehydrogenation catalyst having a Geldart A or Geldart B classification in a fluidized bed at a temperature from 550° C. to 760° C. and a pressure from about 41.4 to about 308.2 kPa (about 6.0 to about 44.7 psia) and a catalyst to feed ratio, w/w, from 5 to 100 to form a dehydrogenate product; separating the dehydrogenate product and unreacted starting feed mixture from a portion of the catalyst by means of a cyclonic separation system; reactivating the catalyst in a fluidized regenerator by combustion at 660° C. to 850° C., followed by contact with an oxygen-containing fluid at 660° C. or greater, and returning the catalyst to the dehydrogenation reactor; (2) compressing the product mixture to form a compressed product mixture; and (3) fractionating the compressed product mixture to form a product stream including at least the target olefin or di-olefin. The integrated process offers increased plant capacity, improved economics, and reduced environmental impact in comparison with other known and conventional processes.
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The invention claimed is: 1. An integrated process for producing C3-C4 olefins or C3-C4 di-olefins comprising the steps of: (1) (a) contacting, in a fluidized dehydrogenation reactor, (i) a C3-C4 hydrocarbon feed and (ii) a catalyst feed comprising a catalyst meeting the requirements of a Geldart A or Geldart B classification; at a ratio of catalyst feed to C3-C4 hydrocarbon feed of from 5 to 100 on a weight to weight basis; wherein the average contact time between the C3-C4 hydrocarbon feed and the catalyst feed is from about 1 second to about 10 seconds; and wherein the reaction temperature in the fluidized dehydrogenation reactor is from about 550° C. to about 750° C.; and wherein the pressure in the fluidized dehydrogenation reactor is from 6.0 to 44.7 pounds per square inch absolute at the outlet of the reactor; under conditions such that a step (1)(a) product mixture, comprising a C3-C4 target olefin or di-olefin, hydrogen and unreacted C3-C4 hydrocarbon feed, is formed; and the catalyst has coke deposited thereon and is at least partially deactivated such that it forms an at least partially deactivated catalyst; and (b) transferring the step (1)(a) product mixture and the at least partially deactivated catalyst from the fluidized dehydrogenation reactor to a cyclonic separation system, and under conditions such that (i) the step (1)(a) product mixture and the at least partially deactivated catalyst remain in contact, at the reaction temperature and after the transfer to the cyclonic separation system, for an average time of from 0 seconds to less than about 10 seconds, and (ii) the step (1)(a) product mixture is converted to form a step (1)(b) product mixture; and thereafter substantially separating the step (1)(b) product mixture and the at least partially deactivated catalyst from each other; (c) transferring at least a portion of the at least partially deactivated catalyst to a regenerator vessel and heating the at least partially deactivated catalyst therein to a combustion temperature of from about 660° C. to about 850° C. in order to combust the coke deposited on the at least partially deactivated catalyst therein, using heat generated by the coke combustion itself and also by a supplemental fuel, the heating forming a heated, further deactivated catalyst which has an activity for dehydrogenating the C3-C4 hydrocarbon feed that is less than that of the at least partially deactivated catalyst, and, (d) subjecting the heated, further deactivated catalyst to a conditioning step, comprising maintaining the heated, further deactivated catalyst at a temperature of at least 660° C. under a flow of an oxygen-containing gas for more than 2 minutes, to form an oxygen-containing, at least partially reactivated catalyst that has an activity for dehydrogenating the C3-C4 hydrocarbon feed that is greater than that of the at least partially deactivated catalyst; and (e) transferring the at least partially reactivated catalyst back to the fluidized dehydrogenation reactor; (2) transferring the step (1)(b) product mixture to a compressor, wherein the step (1)(b) product mixture is compressed at least once to form a step (2) product mixture; and (3) transferring the step (2) product mixture to a product recovery area, wherein the step (2) product mixture is separated into recovered products comprising at least one or more target C3-C4 olefin or di-olefin fractions. 2. The process of claim 1 , wherein the catalyst comprises gallium and platinum on an alumina or alumina silica support. 3. The process of claim 1 , wherein the C3 hydrocarbon in the C3-C4 hydrocarbon feed is propane and the step (3) product mixture comprises a propylene fraction. 4. The process of claim 1 , being retrofitted in a plant previously comprising a reaction system comprising multiple adiabatic reactors arranged in a series. 5. The process of claim 1 , being retrofitted in a plant previously comprising a reaction system comprising multiple fixed bed dehydrogenation reactors deployed in parallel. 6. The process of claim 4 , wherein the retrofitted plant has a capacity that is at least 5 percent greater than that of a non-retrofitted plant. 7. The process of claim 1 , wherein the fluidized dehydrogenation reactor comprises a lower section operating as a fast fluidized or turbulent bed, and an upper section operating as a riser, and wherein the average catalyst flow and the average gas flow are concurrently upward. 8. The process of claim 1 , where the combustion in the regenerator occurs in either a combustor comprising a lower section operating as a fast fluidized, turbulent, or bubbling bed, and an upper section operating as a riser, wherein the average catalyst flow and average gas flow are concurrently upward; or in a combustor comprising a fast fluidized, turbulent, or bubbling bed, wherein the average catalyst flow is downward and the average gas flow is upward. 9. The process of claim 1 , wherein the conditioning step occurs in a fast fluidized, turbulent or bubbling bed regenerator, wherein the average catalyst flow is downward and the average gas flow is upward. 10. The process of claim 1 , wherein hydrogen is not recycled from step (3) to step (1)(a). 11. The process of claim 1 including as an additional step stripping the catalyst between step (1)(b) and step (1)(c). 12. The process of claim 11 , wherein: the step (2) product mixture is separated into recovered products comprising at least one or more target C3-C4 olefin or di-olefin fractions, and one or more additional fractions selected from an unreacted C3-C4 hydrocarbon feed fraction; a light gas fraction; a heavies fraction; a by-products fraction; and combinations thereof; and wherein at least a portion of the unreacted C3-C4 hydrocarbon feed fraction is recycled back to step (1)(a); and the light gas fraction is transferred to step (1)(c) to serve as the supplemental fuel.
Liquid · CPC title
by an ascending fluid · CPC title
with control of oxygen content in oxidation gas · CPC title
moved by gravity in a downward flow · CPC title
of gallium, indium or thallium · CPC title
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