WO2023212497A1 - Processes for catalytic paraffin dehydrogenation and catalyst recovery - Google Patents

Processes for catalytic paraffin dehydrogenation and catalyst recovery Download PDF

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Publication number
WO2023212497A1
WO2023212497A1 PCT/US2023/065960 US2023065960W WO2023212497A1 WO 2023212497 A1 WO2023212497 A1 WO 2023212497A1 US 2023065960 W US2023065960 W US 2023065960W WO 2023212497 A1 WO2023212497 A1 WO 2023212497A1
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Prior art keywords
catalyst
metal oxide
effluent stream
reactor
oxide catalyst
Prior art date
Application number
PCT/US2023/065960
Other languages
French (fr)
Inventor
Michael J. Tallman
Manoj NAGVEKAR
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Kellogg Brown & Root Llc
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Publication date
Priority claimed from US17/728,501 external-priority patent/US20220250049A1/en
Application filed by Kellogg Brown & Root Llc filed Critical Kellogg Brown & Root Llc
Publication of WO2023212497A1 publication Critical patent/WO2023212497A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/42—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor
    • C07C5/48—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor with oxygen as an acceptor
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00—Regeneration or reactivation of catalysts, in general
    • B01J38/04—Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
    • B01J38/12—Treating with free oxygen-containing gas
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J38/00—Regeneration or reactivation of catalysts, in general
    • B01J38/48—Liquid treating or treating in liquid phase, e.g. dissolved or suspended
    • B01J38/50—Liquid treating or treating in liquid phase, e.g. dissolved or suspended using organic liquids
    • B01J38/56—Hydrocarbons

Definitions

  • the present invention relates to a process for dehydrogenation of paraffins by reacting a paraffin stream with metal oxide catalyst(s) to produce light olefins, such as propylene, and a process for the recovery of metal oxide catalyst fines from the reactor effluent stream using a wash fluid and filtration.
  • a potential deficiency in processes for alkane or paraffin dehydrogenation employing a riser or fluidized-bed type reactor is the amount of catalyst fines in the effluent streams leaving the dehydrogenation reactor.
  • a water quench tower is used to cool the reactor effluent and condense the water therein, particularly if dilution steam is used to lower the partial pressure of the alkane or paraffin.
  • the catalyst fines contained in the reactor effluent stream cannot easily be separated from quench water, leading to excessive fouling in the equipment and consequential high maintenance costs.
  • FIGURE is a schematic illustration of a process for catalytic paraffin dehydrogenation and catalyst recovery of the kind described herein.
  • a process for dehydrogenating paraffins by contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms in a riser, fluidized bed, or fixed-bed swing reactor for a reaction period ranging from about 0.05 seconds to about 10 minutes.
  • the metal oxide catalyst includes an active catalyst including, but not necessarily limited to, zinc, copper, iron, manganese, niobium, and combinations thereof; a catalyst support including, but not necessarily limited to, titanium, aluminum, silicon, and combinations thereof; and a catalyst stabilizer including, but not necessarily limited to, zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, niobium, tungsten, and combinations thereof, wherein the metal oxide catalyst is substantially free of platinum and chromium.
  • an active catalyst including, but not necessarily limited to, zinc, copper, iron, manganese, niobium, and combinations thereof
  • a catalyst support including, but not necessarily limited to, titanium, aluminum, silicon, and combinations thereof
  • a catalyst stabilizer including, but not necessarily limited to, zirconium, cerium, dyspros
  • a process for recovering catalyst fines from the reactor effluent stream of a catalytic paraffin dehydrogenation reaction in a riser or fluidized-bed type reactor comprising: contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms; generating a reactor effluent stream comprising metal oxide catalyst fines after contacting the metal oxide catalyst with the paraffin; and contacting the reactor effluent stream with a wash fluid to transfer the metal oxide catalyst fines from the reactor effluent stream into the wash fluid and form a cooled catalyst effluent stream and a substantially catalyst-free product stream.
  • catalyst fines may be recovered by contacting the effluent stream of the reactor with a wash fluid, typically oil or water, to form a cooled catalyst effluent stream and a substantially catalyst-free product stream and then filtering the cooled catalyst effluent stream with a set of filters to capture the catalyst fines for potential reuse.
  • a wash fluid typically oil or water
  • the paraffin to be contacted with the metal oxide catalyst(s) may be propane, ethane, n-butane, isobutane, and combinations thereof.
  • the paraffin may be introduced to the reactor with or without an inert diluent or steam.
  • the metal oxide catalysts useful in dehydrogenating the paraffin to produce a light olefin product gas may be made up of one or more of the following oxides: zinc, titanium, copper, iron, manganese, aluminum, silicon, zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, tungsten, or niobium.
  • the metal oxide catalyst(s) used are substantially free of platinum and chromium.
  • the metal oxide catalyst has three sub-groups: active catalyst, support, and stabilizer.
  • the active catalyst includes, but is not necessarily limited to, zinc, copper, iron, manganese, niobium, and combinations thereof.
  • the catalyst support includes, but is not necessarily limited to, titanium, aluminum, silicon, and combinations thereof.
  • the catalyst stabilizer includes, but is not necessarily limited to, zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, niobium, tungsten, and combinations thereof.
  • zirconium is not an active catalyst component, but is only a stabilizer for the metal oxide catalyst
  • the dehydrogenation of the paraffin using metal oxide catalysts of the kinds described above and recovery of catalyst fines in the reactor effluent stream may be accomplished, in one non-limiting embodiment, by the process depicted in the FIGURE in which a paraffin feedstock 10 comprising paraffins having 2-8 carbons is contacted with one or more metal oxide catalysts in a riser or fluidized bed reactor under dehydrogenation conditions.
  • This process may be performed at a reaction temperature of 500-800°C, a space velocity of 0.1 -1 tr 1 , and a pressure of 0.01-0.2 MPa.
  • the reaction period may range from about 0.05 seconds to about 10 minutes.
  • the dehydrogenation reaction between the paraffin and the metal oxide catalyst(s) may also be carried out in a fixed-bed swing or riser or fluidized- bed reactor from which a reactor outlet stream 20 is formed.
  • the reactor outlet stream 20, in one non-restrictive embodiment, is then sent to a cyclone or disengager to separate catalyst from the reactor outlet stream and form an overhead reactor effluent stream 30.
  • the reactor effluent stream 30 contains light olefins, such as, without limitation, propylene and/or ethylene.
  • the bulk of the catalyst is retained within the reactor or recovered in the cyclone/disengager and then sent as a separated catalyst stream 40 to a regenerator, which uses combustion air 50 to produce a flue gas stream 60 and a regenerated catalyst stream 70 that is returned to the reactor.
  • some catalyst fines may be contained in the reactor effluent stream 30.
  • These metal oxide catalyst fines may be recovered in a process in which the reactor effluent stream 30 is contacted in a quench tower with a wash fluid 90, typically oil or water, to transfer the metal oxide catalyst fines from the reactor outlet stream into the wash fluid and form a cooled catalyst effluent stream 100 and a substantially catalyst-free product stream 80.
  • the reactor effluent stream 30 is contacted with the wash fluid in a quench tower that contains vapor-liquid contacting elements, such as, without limitation, packing or trays.
  • the quench tower in another embodiment, may also have a recirculation loop for continuously recirculating a wash fluid to the contacting elements.
  • the cooled catalyst effluent stream 100 may subsequently be converted into a slurry and then directed to one or more filters to separate the metal oxide catalyst fines.
  • the slurry is continuously passed through a first filter in a filtration mode to separate the metal oxide catalyst fines therefrom while a second filter in parallel with the first filter is in backflushing mode to remove the separated metal oxide catalyst fines therefrom.
  • the filtration of the slurry may comprise periodically alternating the first and the second filters between filtration and backflushing mode.
  • the separated metal oxide catalyst fines may be collected and accumulated in a catalyst accumulator. The catalyst fines may then be prepared for reuse in the dehydrogenation reaction.
  • the present invention may be practiced in the absence of an element not disclosed.
  • the present invention may suitably comprise, consist or consist essentially of the elements disclosed.
  • the process may comprise, consist of, or consist essentially of: contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms in a reactor for a reaction period ranging from about 0.05 seconds to about 10 minutes.
  • the recovery of the catalyst fines from a reactor effluent stream may comprise, consist of, or consist essentially of: contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms, generating a reactor effluent stream comprising metal oxide catalyst fines after contacting the metal oxide catalyst with the paraffin, and contacting the reactor effluent stream with a wash fluid to transfer the metal oxide catalyst fines from the reactor effluent stream into the wash fluid and form a cooled catalyst effluent stream and a substantially catalyst-free product stream.
  • the present invention may suitably comprise, consist of, or consist essentially of the elements disclosed and may be practiced in the absence of an element not disclosed.
  • a process for dehydrogenating paraffins comprising, consisting essentially of, or consisting of, contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms for a reaction period ranging from about 0.05 seconds to about 10 minutes in a reactor for a catalytic paraffin dehydrogenation reaction
  • the metal oxide catalyst comprises, consists essentially of, or consists of an active catalyst selected from the group consisting of zinc, copper, manganese, niobium, and combinations thereof
  • a catalyst support selected from the group consisting of titanium, aluminum, silicon, and combinations thereof
  • a catalyst stabilizer selected from the group consisting of zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium

Abstract

A paraffin having 2-8 carbon atoms may be dehydrogenated by contacting the paraffin with metal oxide catalyst(s) to produce light olefins, such as propylene, under certain reaction conditions in a riser, fluidized bed, or fixed-bed swing reactor. The resulting metal oxide catalyst fines contained in the reactor effluent stream formed by the dehydrogenation reaction may be recovered by contacting the reactor effluent stream with a wash fluid to form a catalyst effluent stream that is subsequently slurried and filtered to capture the catalyst fines for potential reuse.

Description

PROCESSES FOR CATALYTIC PARAFFIN DEHYDROGENATION AND CATALYST RECOVERY
CROSS-REFERENCE TO RELATED APPLICATION
[0001] This application claims priority to U.S. Application Serial No. 17/728,501 filed April 25, 2022, incorporated herein in its entirety by reference.
TECHNICAL FIELD
[0002] The present invention relates to a process for dehydrogenation of paraffins by reacting a paraffin stream with metal oxide catalyst(s) to produce light olefins, such as propylene, and a process for the recovery of metal oxide catalyst fines from the reactor effluent stream using a wash fluid and filtration.
BACKGROUND
[0003] The abundance of alkanes and paraffins from shale and stranded gas has spurned the development of more cost-effective ways to produce light olefins, the demand for which has increased significantly in recent years. Steam cracker units using lighter shale condensates as feedstock have been used to meet the increase in the demand for light olefins, like ethylene. However, these units have been found to be deficient for propylene production due to the low propylene/ethylene ratio and low propylene yield. As a result, finding routes for the targeted production of propylene have received considerable interest.
[0004] It has been shown that catalytic dehydrogenation provides the possibility of high selectivity to a single olefin product. Current alkane dehydrogenation processes for the production of propylene and other light olefins employ the use of platinum-based and chromium-based catalysts. Given the expense associated with platinum and the carcinogenic properties of chromium, there is a need for developing less expensive, less toxic metal oxide catalysts that can is capable of good alkene selectivity during the dehydrogenation process and a correspondingly high yield.
[0005] A potential deficiency in processes for alkane or paraffin dehydrogenation employing a riser or fluidized-bed type reactor is the amount of catalyst fines in the effluent streams leaving the dehydrogenation reactor. With regard to the reactor effluent stream, a water quench tower is used to cool the reactor effluent and condense the water therein, particularly if dilution steam is used to lower the partial pressure of the alkane or paraffin. The catalyst fines contained in the reactor effluent stream cannot easily be separated from quench water, leading to excessive fouling in the equipment and consequential high maintenance costs. Thus, there is also a need for improved recovery of catalyst fines found in the effluent stream from the dehydrogenation reactor.
BRIEF DESCRIPTION OF THE DRAWINGS
[0006] The FIGURE is a schematic illustration of a process for catalytic paraffin dehydrogenation and catalyst recovery of the kind described herein.
SUMMARY
[0007] There is provided, in one form, a process for dehydrogenating paraffins by contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms in a riser, fluidized bed, or fixed-bed swing reactor for a reaction period ranging from about 0.05 seconds to about 10 minutes. In one embodiment, the metal oxide catalyst includes an active catalyst including, but not necessarily limited to, zinc, copper, iron, manganese, niobium, and combinations thereof; a catalyst support including, but not necessarily limited to, titanium, aluminum, silicon, and combinations thereof; and a catalyst stabilizer including, but not necessarily limited to, zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, niobium, tungsten, and combinations thereof, wherein the metal oxide catalyst is substantially free of platinum and chromium.
[0008] There is further provided in another form, a process for recovering catalyst fines from the reactor effluent stream of a catalytic paraffin dehydrogenation reaction in a riser or fluidized-bed type reactor, the process comprising: contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms; generating a reactor effluent stream comprising metal oxide catalyst fines after contacting the metal oxide catalyst with the paraffin; and contacting the reactor effluent stream with a wash fluid to transfer the metal oxide catalyst fines from the reactor effluent stream into the wash fluid and form a cooled catalyst effluent stream and a substantially catalyst-free product stream.
DETAILED DESCRIPTION
[0009] It has been discovered that contacting one or more metal oxide catalysts with a paraffin having 2-8 carbon atoms in a dehydrogenation reaction for a period ranging from about 0.05 seconds to about 10 minutes in a reactor may lead to better selectively for the production of certain olefins, such as propylene and ethylene. It has also been discovered that metal oxide catalyst fines, generated because of attrition in a riser or fluidized-bed type reactor, are contained within the reactor effluent stream. These catalyst fines may be recovered by contacting the effluent stream of the reactor with a wash fluid, typically oil or water, to form a cooled catalyst effluent stream and a substantially catalyst-free product stream and then filtering the cooled catalyst effluent stream with a set of filters to capture the catalyst fines for potential reuse.
[0010] In one embodiment, the paraffin to be contacted with the metal oxide catalyst(s) may be propane, ethane, n-butane, isobutane, and combinations thereof. In another embodiment, the paraffin may be introduced to the reactor with or without an inert diluent or steam.
[0011] The metal oxide catalysts useful in dehydrogenating the paraffin to produce a light olefin product gas may be made up of one or more of the following oxides: zinc, titanium, copper, iron, manganese, aluminum, silicon, zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, tungsten, or niobium. In a non-limiting embodiment, the metal oxide catalyst(s) used are substantially free of platinum and chromium. In a non-limiting embodiment, the metal oxide catalyst has three sub-groups: active catalyst, support, and stabilizer. In one non-limiting embodiment, the active catalyst includes, but is not necessarily limited to, zinc, copper, iron, manganese, niobium, and combinations thereof. In another non- restrictive version, the catalyst support includes, but is not necessarily limited to, titanium, aluminum, silicon, and combinations thereof. In a different non-limiting embodiment, the catalyst stabilizer includes, but is not necessarily limited to, zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, niobium, tungsten, and combinations thereof. In particular, zirconium is not an active catalyst component, but is only a stabilizer for the metal oxide catalyst
[0012] The dehydrogenation of the paraffin using metal oxide catalysts of the kinds described above and recovery of catalyst fines in the reactor effluent stream may be accomplished, in one non-limiting embodiment, by the process depicted in the FIGURE in which a paraffin feedstock 10 comprising paraffins having 2-8 carbons is contacted with one or more metal oxide catalysts in a riser or fluidized bed reactor under dehydrogenation conditions. This process may be performed at a reaction temperature of 500-800°C, a space velocity of 0.1 -1 tr1, and a pressure of 0.01-0.2 MPa. In one embodiment, the reaction period may range from about 0.05 seconds to about 10 minutes. In other non-limiting embodiments, the dehydrogenation reaction between the paraffin and the metal oxide catalyst(s) may also be carried out in a fixed-bed swing or riser or fluidized- bed reactor from which a reactor outlet stream 20 is formed. The reactor outlet stream 20, in one non-restrictive embodiment, is then sent to a cyclone or disengager to separate catalyst from the reactor outlet stream and form an overhead reactor effluent stream 30.
[0013] In a non-limiting embodiment, the reactor effluent stream 30 contains light olefins, such as, without limitation, propylene and/or ethylene. The bulk of the catalyst is retained within the reactor or recovered in the cyclone/disengager and then sent as a separated catalyst stream 40 to a regenerator, which uses combustion air 50 to produce a flue gas stream 60 and a regenerated catalyst stream 70 that is returned to the reactor.
[0014] However, some catalyst fines, formed due to attrition in reactor types like riser or fluidized-bed reactors, may be contained in the reactor effluent stream 30. These metal oxide catalyst fines may be recovered in a process in which the reactor effluent stream 30 is contacted in a quench tower with a wash fluid 90, typically oil or water, to transfer the metal oxide catalyst fines from the reactor outlet stream into the wash fluid and form a cooled catalyst effluent stream 100 and a substantially catalyst-free product stream 80. In one non-restrictive embodiment, the reactor effluent stream 30 is contacted with the wash fluid in a quench tower that contains vapor-liquid contacting elements, such as, without limitation, packing or trays. The quench tower, in another embodiment, may also have a recirculation loop for continuously recirculating a wash fluid to the contacting elements.
[0015] In another non-restrictive embodiment, the cooled catalyst effluent stream 100 may subsequently be converted into a slurry and then directed to one or more filters to separate the metal oxide catalyst fines. In one embodiment, the slurry is continuously passed through a first filter in a filtration mode to separate the metal oxide catalyst fines therefrom while a second filter in parallel with the first filter is in backflushing mode to remove the separated metal oxide catalyst fines therefrom. The filtration of the slurry may comprise periodically alternating the first and the second filters between filtration and backflushing mode. After filtration, the separated metal oxide catalyst fines may be collected and accumulated in a catalyst accumulator. The catalyst fines may then be prepared for reuse in the dehydrogenation reaction.
[0016] In the foregoing specification, the invention has been described with reference to specific embodiments thereof. However, the specification is to be regarded in an illustrative rather than a restrictive sense. For example, paraffins, metal oxide catalysts, dehydrogenation reaction conditions and equipment, and catalyst fine recovery conditions and equipment falling within the claimed or disclosed parameters, but not specifically identified or tried in a particular example, are expected to be within the scope of this invention.
[0017] The present invention may be practiced in the absence of an element not disclosed. In addition, the present invention may suitably comprise, consist or consist essentially of the elements disclosed. For instance, the process may comprise, consist of, or consist essentially of: contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms in a reactor for a reaction period ranging from about 0.05 seconds to about 10 minutes.
[0018] Alternatively, the recovery of the catalyst fines from a reactor effluent stream may comprise, consist of, or consist essentially of: contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms, generating a reactor effluent stream comprising metal oxide catalyst fines after contacting the metal oxide catalyst with the paraffin, and contacting the reactor effluent stream with a wash fluid to transfer the metal oxide catalyst fines from the reactor effluent stream into the wash fluid and form a cooled catalyst effluent stream and a substantially catalyst-free product stream.
[0019] The present invention may suitably comprise, consist of, or consist essentially of the elements disclosed and may be practiced in the absence of an element not disclosed. For instance, there is provided a process for dehydrogenating paraffins, the process comprising, consisting essentially of, or consisting of, contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms for a reaction period ranging from about 0.05 seconds to about 10 minutes in a reactor for a catalytic paraffin dehydrogenation reaction wherein: the metal oxide catalyst comprises, consists essentially of, or consists of an active catalyst selected from the group consisting of zinc, copper, manganese, niobium, and combinations thereof; a catalyst support selected from the group consisting of titanium, aluminum, silicon, and combinations thereof; and a catalyst stabilizer selected from the group consisting of zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, niobium, and combinations thereof; and the metal oxide catalyst is free of platinum and chromium.
[0020] The words “comprising” and “comprises” as used throughout the claims, are to be interpreted to mean “including but not limited to” and “includes but not limited to”, respectively.
[0021] As used herein, the word “substantially” shall mean “being largely but not wholly that which is specified.”
[0022] As used herein, the singular forms “a,” “an,” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. [0023] As used herein, the term “about” in reference to a given parameter is inclusive of the stated value and has the meaning dictated by the context (e.g., it includes the degree of error associated with measurement of the given parameter).
[0024] As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.

Claims

CLAIMS What is claimed is:
1. A process for recovering catalyst fines from a reactor effluent stream of a catalytic paraffin dehydrogenation reaction, the process comprising: a. causing a reaction by contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms for a reaction period ranging from about 0.05 seconds to about 10 minutes in a reactor for a catalytic paraffin dehydrogenation reaction wherein: the metal oxide catalyst consisting essentially of: an active catalyst selected from the group consisting of zinc, copper, iron, manganese, niobium, and combinations thereof; a catalyst support comprising titanium, aluminum, or silicon,; and a catalyst stabilizer comprising zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, niobium, or tungsten; and wherein the metal oxide catalyst is free of platinum and chromium; b. generating a reactor effluent stream comprising metal oxide catalyst fines after contacting with the metal oxide catalyst with the paraffin; and c. contacting the reactor effluent stream with a wash fluid to transfer the metal oxide catalyst fines from the reactor effluent stream into the wash fluid and form a cooled catalyst effluent stream and a catalyst-free product stream.
2. The process of claim 1 , wherein the reactor is a riser reactor, fluidized bed reactor, or a fixed-bed swing reactor. The process of claim 1 , wherein the paraffin is selected from a group consisting of propane, ethane, n-butane, isobutane, and combinations thereof. The process of claim 1 , further comprising generating a reactor effluent stream comprising an olefin. The process of claim 4, wherein the olefin is selected from a group consisting of propylene, ethylene, and combinations thereof. The process of claim 1 , wherein the reaction occurs at a temperature ranging from about 500°C to about 800°C. The process of claim 1 , wherein the reaction occurs at a pressure ranging from about 0.01 MPa to about 0.02 MPa. The process of claim 1 , wherein the paraffin is introduced to the reactor with an inert diluent or steam. The process of claim 1 , wherein the active catalyst is selected from the group consisting of zinc, copper, manganese, niobium, and combinations thereof. A process for recovering catalyst fines from a reactor effluent stream of a catalytic paraffin dehydrogenation reaction, the process comprising: a. contacting a metal oxide catalyst with a paraffin having 2-8 carbon atoms in a reactor; i. wherein the paraffin is selected from a group consisting of propane, n-butane, isobutane, and combinations thereof; ii. wherein the metal oxide catalyst consists essentially of: an active catalyst selected from the group consisting of zinc, copper, iron, manganese, niobium, and combinations thereof; a catalyst support selected from the group consisting of titanium, aluminum, silicon, and combinations thereof; and a catalyst stabilizer selected from the group consisting of zirconium, cerium, dysprosium, erbium, europium, gadolinium, lanthanum, neodymium, praseodymium, samarium, terbium, ytterbium, yttrium, niobium, tungsten, and combinations thereof; and; iii. wherein the metal oxide catalyst is free of platinum and chromium; b. generating a reactor effluent stream comprising metal oxide catalyst fines after contacting with the metal oxide catalyst with the paraffin; and c. contacting the reactor effluent stream with a wash fluid to transfer the metal oxide catalyst fines from the reactor effluent stream into the wash fluid and form a cooled catalyst effluent stream and a catalyst- free product stream. The process of claim 10, further comprising converting the cooled catalyst effluent stream into a slurry. The process of claim 11 , further comprising directing the slurry to one or more filters to separate the metal oxide catalyst fines. The process of claim 12, wherein the slurry is continuously passed through a first filter in a filtration mode to separate the metal oxide catalyst fines therefrom while a second filter in parallel with the first filter is in backflushing mode to remove the separated metal oxide catalyst fines therefrom. The process of claim 13, wherein the filtration of the slurry comprises periodically alternating the first and the second filters between filtration and backflushing modes. The process of claim 13, wherein the separated metal oxide catalyst fines are accumulated in a catalyst accumulator. The process of claim 10, wherein the reactor effluent stream is contacted with the wash fluid in a quench tower. The process of claim 16, wherein the quench tower has vapor-liquid contacting elements. The process of claim 16, wherein the quench tower has a recirculation loop for continuously recirculating a wash oil to contacting elements. The process of claim 16, wherein the wash fluid comprises oil or water.
PCT/US2023/065960 2022-04-25 2023-04-19 Processes for catalytic paraffin dehydrogenation and catalyst recovery WO2023212497A1 (en)

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US20040069684A1 (en) * 2002-10-10 2004-04-15 Kellogg Brown & Root, Inc. Catalyst recovery from light olefin FCC effluent
US20100236985A1 (en) * 2009-03-19 2010-09-23 Lin Luo Dehydrogenation process and catalyst
US20140371504A1 (en) * 2013-06-18 2014-12-18 Uop Llc Fluidized catalyst circulation reactor for paraffin oxydative dehydrogenation
US20170233312A1 (en) * 2016-02-12 2017-08-17 King Fahd University Of Petroleum And Minerals Fluidizable catalyst for oxidative dehydrogenation of alkanes to olefins in an oxygen free environment
US20200101445A1 (en) * 2018-09-28 2020-04-02 Exelus, Inc. Mixed Metal Oxide Catalyst useful for Paraffin Dehydrogenation
US20200299212A1 (en) * 2019-03-21 2020-09-24 Kellogg Brown & Root Llc Processes for catalytic paraffin dehydrogenation and catalyst recovery
US20220250049A1 (en) * 2019-03-21 2022-08-11 Kellogg Brown & Root Llc Processes for catalytic paraffin dehydrogenation and catalyst recovery

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040069684A1 (en) * 2002-10-10 2004-04-15 Kellogg Brown & Root, Inc. Catalyst recovery from light olefin FCC effluent
US20100236985A1 (en) * 2009-03-19 2010-09-23 Lin Luo Dehydrogenation process and catalyst
US20140371504A1 (en) * 2013-06-18 2014-12-18 Uop Llc Fluidized catalyst circulation reactor for paraffin oxydative dehydrogenation
US20170233312A1 (en) * 2016-02-12 2017-08-17 King Fahd University Of Petroleum And Minerals Fluidizable catalyst for oxidative dehydrogenation of alkanes to olefins in an oxygen free environment
US20200101445A1 (en) * 2018-09-28 2020-04-02 Exelus, Inc. Mixed Metal Oxide Catalyst useful for Paraffin Dehydrogenation
US20200299212A1 (en) * 2019-03-21 2020-09-24 Kellogg Brown & Root Llc Processes for catalytic paraffin dehydrogenation and catalyst recovery
US20220250049A1 (en) * 2019-03-21 2022-08-11 Kellogg Brown & Root Llc Processes for catalytic paraffin dehydrogenation and catalyst recovery

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