WO2017221179A1 - Conversion de catalyseurs à base de chrome désactivé - Google Patents

Conversion de catalyseurs à base de chrome désactivé Download PDF

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Publication number
WO2017221179A1
WO2017221179A1 PCT/IB2017/053712 IB2017053712W WO2017221179A1 WO 2017221179 A1 WO2017221179 A1 WO 2017221179A1 IB 2017053712 W IB2017053712 W IB 2017053712W WO 2017221179 A1 WO2017221179 A1 WO 2017221179A1
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Prior art keywords
chromium
catalyst
deactivated
metal
oxide
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Ceased
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PCT/IB2017/053712
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English (en)
Inventor
YongMan CHOI
Ramsey BUNAMA
Khalid Mohammed EL-YAHYAOUI
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SABIC Global Technologies BV
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SABIC Global Technologies BV
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Publication of WO2017221179A1 publication Critical patent/WO2017221179A1/fr
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    • 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/85—Chromium, molybdenum or tungsten
    • B01J23/86—Chromium
    • B01J23/868—Chromium copper and chromium
    • 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/002—Mixed oxides other than spinels, e.g. perovskite
    • 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/90—Regeneration or reactivation
    • B01J23/94—Regeneration or reactivation of catalysts comprising metals, oxides or hydroxides of the iron group metals or copper
    • 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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation
    • 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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/08—Heat treatment
    • 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
    • B01J38/68—Liquid treating or treating in liquid phase, e.g. dissolved or suspended including substantial dissolution or chemical precipitation of a catalyst component in the ultimate reconstitution of the catalyst

Definitions

  • chromia alumina catalyst For example, it can be used to produce isobutylene, propylene or isoprene from isobutane, propane or isopentane, respectively.
  • the process is an adiabatic, cyclic process. Each cycle comprises several steps, including catalyst reduction, dehydrogenation, purging of the remaining hydrocarbon from the reactor, and finally a regeneration step with air. The cycle then starts again with the reduction step.
  • the dehydrogenation reaction is highly endothermic. Therefore, the temperature of the catalyst bed decreases during the dehydrogenation step. This decrease in temperature causes a decrease in paraffin conversion.
  • the reactor In order to reheat the catalyst bed and remove coke that has deposited on the catalyst during the dehydrogenation step, the reactor is typically purged of hydrocarbon and then undergoes a regeneration step with air. Heat is provided to the bed by the hot air that passes through the bed and also by the combustion of the coke deposits on the catalyst. Reduction of the catalyst, with a reducing gas such as hydrogen, prior to dehydrogenation step also provides some additional heat.
  • Chromium-based catalysts used in CATOFIN® process are often regenerated with heat-generating materials (HGM) used in CATOFIN® reactors.
  • HGM heat-generating materials
  • the catalysts are physically mixed with the heat-generating materials to transfer the extra heat released from the reduction and oxidation reactions of heat-generating materials with reducing gases (such as H 2 , CH 4 , and CO) and oxidizing gases (such as air).
  • the primary heat- generating materials include CuO and Cu.
  • the extra heat is transferred to the endothermic dehydrogenation of hydrocarbons on chromium-based catalysts, which improves the yield.
  • the copper and chromium based components from the heat-generating materials and the catalysts are fused, actually resulting in deactivation of the catalysts and heat-generating materials.
  • a method for generating supported metal chromium oxide catalysts comprises: providing a deactivated chromium-based catalyst; determining the amount of chromium in the deactivated chromium-based catalyst by inductively coupled plasma atomic emission spectroscopy; combining a calculated amount of a metal material with the deactivated chromium-based catalyst to form a mixture, wherein the calculated amount is based on the determined amount of chromium in the deactivated chromium-based catalyst to yield a desired stoichiometry of the metal chromium oxide catalyst; drying the mixture at a temperature of at least 100 °C; and calcining the dried mixture at a temperature of at least 250 °C to form the metal chromium oxide catalysts
  • a method for generating a supported metal chromium oxide catalyst comprising: combining a deactivated chromium-based catalyst with a copper oxide based heat generating material to form a mixture; drying the mixture at a temperature of at least 100 °C; and calcining the dried mixture at a temperature of at least 250 °C to form the supported metal chromium oxide catalyst.
  • the present disclosure provides methods for generating a supported metal chromium oxide catalyst.
  • the present methods can be used to generate copper chromium oxides.
  • the metal chromium oxide catalyst can be of the formula Cu x Cr y O z , wherein x is 1 to 2, y is 1 to 2, and z is 4 to 5.
  • Specific examples of the metal chromium oxide catalysts that can be generated include CuCr0 4 , CuCr 2 0 4 , Cu 2 Cr0 4 , and Cu 2 Cr 2 0s, among others.
  • Copper chromite CuCr 2 0 4
  • the present methods can be used to regenerate the deactivated chromium-based catalysts with heat-generating materials, which avoid merely fusing the heat-generating materials and chromium-based catalysts together, which results in further deactivation of the catalysts.
  • the method can include providing a deactivated chromium-based catalyst and determining the amount of chromium in the deactivated chromium-based catalyst by inductively coupled plasma atomic emission spectroscopy. Based on the amount of chromium in the deactivated chromium-based catalyst, the amount of a heat generating material and/or metal can be calculated to yield a desired stoichiometry of the metal chromium oxide catalyst (e.g., M, Cr). In other words, the specific metal chromium oxide catalyst can be synthesized based on the molar ratio used of chromium and metal, such as copper or nickel, used during the mixing step.
  • the metal chromium oxide catalyst e.g., M, Cr
  • the desired stoichiometry of the metal chromium oxide catalyst can be a 5: 1 molar ratio of metal to chromium to a 1:5 molar ratio of metal to chromium.
  • a desired stoichiometry of the metal chromium oxide catalyst can be a 1: 1 molar ratio of metal to chromium.
  • the deactivated chromium-based catalyst and calculated amount of metal can be combined to form a mixture that is dried at a temperature of at least 100 °C, and then can be calcined at a temperature of at least 250 °C to form the metal chromium oxide catalysts.
  • the dried mixture can be calcined at a temperature of 300-600 °C, for example, 600 °C.
  • the heat generating material can be a heat releasing material.
  • the heat releasing material can be any desirable material that releases heat during reduction and regeneration processes.
  • the heat releasing material may be copper oxide and/or nickel oxide, among others.
  • the deactivated chromium-based catalyst can include a chromium oxide dehydrogenation catalyst manufactured on an alumina support.
  • the deactivated chromium-based catalyst can include Cr 2 0 3 and A1 2 0 3 .
  • the catalyst may be adapted to incorporate other metals or metal oxide catalysts.
  • metals or metal oxides thereof include, but are not limited to, aluminum, magnesium, zirconium, titanium, vanadium, nickel, rhodium, rhenium, iron, silicon, molybdenum, thorium, manganese, cerium, silver, lead, cadmium, calcium, antimony, tin, bismuth, cobalt, tungsten, and zinc.
  • the dehydrogenation catalyst may be adapted to incorporate dehydrogenation catalysts, in lieu of the Cr, such as zeolites, acid treated metal oxides (e.g.
  • Zeolites are microporous, aluminosilicate minerals. Some of the more common mineral zeolites are analcime, chabazite, clinoptilolite, heulandite, natrolite, phillipsite, and stilbite.
  • Synthetic catalysts may include composites of silica and alumina or other metal oxides, including silica-alumina, silica-magnesia, silica-zirconia, silica-thoria, silica-beryllia, silica-titania, silicavanadia, as well as ternary combinations such as silica-alumina-magnesia, silica-alumina-zirconia, and silica-magnesia- zirconia.
  • Other bifunctional catalysts include, platinum and/or rhodium doped zeolites, and platinum-alumina.
  • Acid treated natural clays which may be desirable for use as the catalyst include kaolins, sub-bentonites, montmorillonite, fullers earth, and halloysite.
  • the heat transfer media is copper.
  • the copper heat transfer material may be in a reduced state, i.e. elemental copper.
  • the copper present in the dehydrogenation catalyst bed composition may be in a higher oxidation state (e.g. Cu 1+ or Cu 2+ ).
  • the copper may be in an oxide form, for example CuO.
  • Cu of the present process is selected as heat transfer media because it can easily oscillate between higher and lower oxidation states and produce heat during both oxidation and reduction reactions, whereby the heat generated may be utilized in subsequent dehydrogenation reactions.
  • the present process may be adapted to incorporate other heat releasing media, in lieu of, or in addition to Cu, wherein the heat releasing media is inert to dehydrogenation reactions.
  • Other such heat releasing media may include, but is not limited to, silver, gold, aluminum, tungsten, platinum, etc., as long as it is inert to the dehydrogenation reaction and to produce heat from the reduction and regeneration processes.
  • the dehydrogenation catalyst can comprise 1 wt% to 20 wt%, for example, 1 wt% to 10 wt% or 5 wt% to 15 wt% of the heat transfer media relative to the total weight of the dehydrogenation catalyst.
  • the catalyst can include a support which refers to a high surface area material to which a catalyst is affixed.
  • the support may be inert or may participate in catalytic reactions.
  • the catalyst support can be inert to the dehydrogenation reaction.
  • the reactivity of heterogeneous catalysts and nanomaterial-based catalysts occurs at the surface atoms. Consequently great effort is made to maximize the surface area of a catalyst by distributing it over the support.
  • Typical supports include various kinds of carbon, alumina, and silica.
  • the catalyst support is aluminum oxide.
  • the catalyst support may be comprised of a plurality of different crystallographic phases.
  • the catalyst support may comprise a- AI2O3, ⁇ - ⁇ 1 2 03, ⁇ - ⁇ 1 2 0 3 , ⁇ - ⁇ 1 2 0 3 , ⁇ - ⁇ 1 2 0 3 , ⁇ - ⁇ 1 2 0 3 , and ⁇ - ⁇ 1 2 0 3 , or a combination comprising at least one of the foregoing, for example, the catalyst support is ⁇ - ⁇ 1 2 0 3 , or the catalyst support is ⁇ - ⁇ 1 2 0 3 .
  • an important characteristic of the catalyst support is its ability to store and distribute heat to aid in the catalytic process.
  • One measure of the ability to distribute heat is the thermal conductivity. Heat transfer occurs at a higher rate across materials of high thermal conductivity than across materials of low thermal conductivity.
  • One measure of the ability to store heat is the specific heat capacity. Heat capacity is a measurable physical quantity equal to the ratio of the heat added to (or subtracted from) an object to the resulting temperature change. Heat capacity is an extensive property of matter, meaning it is proportional to the size of the system. When expressing the same phenomenon as an intensive property, the heat capacity is divided by the amount of substance, mass, or volume, so that the quantity is independent of the size or extent of the sample.
  • the specific heat capacity is the heat capacity per unit mass of a material. Temperature reflects the average randomized energy of constituent particles of matter (e.g. atoms or molecules), while heat is the transfer of thermal energy across a system boundary into the body or from the body to the environment. Translation, rotation, and a combination of the two types of energy in the vibration (kinetic and potential) of atoms represent the degrees of freedom of motion which classically contribute to the heat capacity of matter. On a microscopic scale, each system particle absorbs thermal energy among the few degrees of freedom available to it, and at sufficient temperatures, this process contributes to the specific heat capacity. Therefore, a catalyst support with a high specific heat capacity, such as A1 2 0 3 , is advantageous.
  • the mixing of the deactivated chromium-based catalyst with the heat generating material can be performed via a wet impregnation method or a solid state method.
  • the mixing is performed via a wet impregnation method, wherein the heat generating material is copper.
  • the copper can be provided by a precursor of copper nitrate.
  • the deactivated chromium-based catalyst is mixed with the heat generating material via a solid state method, wherein the heat generating material is copper oxide.
  • deactivated chromium-based catalysts including Cr 2 03 can be crushed to powder to increase the interaction with a second metal such as copper.
  • the powder catalysts can be mixed with a copper-containing material by means of wet impregnation with copper nitrate or with copper oxide for the solid-state reaction.
  • the powder catalyst Before adding the second metal component, the powder catalyst can be characterized to determine the amount of chromium content, for example, using the inductively coupled plasma atomic emission spectroscopy (ICP-AES) technique.
  • the molar ratio of chromium to copper can be prepared based on the desired product.
  • a drying process at 120 °C can be performed for 24 hours, followed by calcination at 300 °C for at least 6 hours to produce the final metal chromium oxide catalyst.
  • the generated metal chromium oxide catalysts can be used in a wide variety of applications.
  • copper chromium catalysts can be used in hydrogenation reactions to produce fatty alcohols.
  • Copper oxide- chromium oxide catalysts can also be used in the detoxification of exhaust gases, in particular from automobile engines that contain aluminum, chromium, and copper oxide as substantial components.
  • the generated copper chromite catalysts can also be used in the oxidation of oxidizable hydrocarbons and carbon monoxide present in the exhaust gases of internal combustion engines.
  • CuO was deposited on Cr 2 0 3 /Al 2 03 using a wet impregnation method.
  • An appropriate amount of Cu(N0 3 ) 2 *3H 2 0 was dissolved in a minimum amount of distilled water such that the molar ratio of Cr to Cu was 1: 1, when mixed with Cr 2 0 3 /Al 2 0 3 powder.
  • the mixture was dried for 12 hours at 120 °C in an oven.
  • Inductively coupled plasma atomic emission spectroscopy technique was used to confirm the deposition amount of CuO on Cr 2 0 3 /Al 2 0 3 ., which was found to be 4.23 wt% Cr and 2.58 wt% Cu.
  • In situ X-ray diffractometer experiments were performed in air from room temperature to 1100 °C to examine the Cr and Cu oxide formation region.
  • the supported copper chromium oxide catalysts were successfully prepared by the reaction of copper and Cr 2 0 3 /Al 2 03. Further, various metal chromium-based oxide catalysts can be synthesized based on the molar ratio used of copper to chromium.
  • Embodiment 1 A method for generating supported metal chromium oxide catalysts, comprising: providing a deactivated chromium-based catalyst; determining the amount of chromium in the deactivated chromium-based catalyst by inductively coupled plasma atomic emission spectroscopy; combining a calculated amount of a metal material with the deactivated chromium-based catalyst to form a mixture, wherein the calculated amount is based on the determined amount of chromium in the deactivated chromium-based catalyst to yield a desired stoichiometry of the metal chromium oxide catalyst; drying the mixture at a temperature of at least 100 °C; and calcining the dried mixture at a temperature of at least 250 °C to form the metal chromium oxide catalysts.
  • Embodiment 2 The method of Embodiment 1, further comprising combining the deactivated chromium-based catalyst with the metal material via a wet impregnation method, wherein the metal material includes copper nitrate.
  • Embodiment 3 The method of any of Embodiments 1-2, further comprising combining the deactivated chromium-based catalyst with the metal material via a solid state method, wherein the metal material includes copper oxide.
  • Embodiment 4 The method of any of Embodiments 1-3, further comprising combining the deactivated chromium-based catalyst with the metal material via a solid state method, wherein the metal material includes nickel oxide.
  • Embodiment 5 The method of any of Embodiments 1-4, wherein the metal chromium oxide catalyst is a copper chromium oxide of the formula Cu x Cr y O z , wherein x is 1 to 2, y is 1 to 2, and z is 4 to 5.
  • Embodiment 6 The method of any of Embodiments 1-5, wherein the dried mixture is calcined at a temperature of 600 °C, wherein the metal chromium oxide catalyst is CuCr0 4 .
  • Embodiment 7 The method of Embodiment 6, wherein the dried mixture is calcined at a temperature of 600 °C.
  • Embodiment 8 The method of any of Embodiments 1-7, wherein a desired stoichiometry of the metal chromium oxide catalyst is a 1 : 1 molar ratio of metal to chromium.
  • Embodiment 9 A method for generating a supported metal chromium oxide catalyst, comprising: combining a deactivated chromium-based catalyst with a copper oxide based heat generating material to form a mixture; drying the mixture at a temperature of at least 100 °C; and calcining the dried mixture at a temperature of at least 250 °C to form the supported metal chromium oxide catalyst.
  • Embodiment 10 The method of Embodiment 9, further comprising combining the deactivated chromium-based catalyst with the copper oxide based heat generating material via a wet impregnation method, wherein the copper oxide based heat generating material includes copper nitrate.
  • Embodiment 11 The method of any of Embodiments 9-10, further comprising combining the deactivated chromium-based catalyst with the copper oxide based heat generating material via a solid state method, wherein the copper oxide based heat generating material includes copper oxide.
  • Embodiment 12 The method of any of Embodiments 9-11, wherein the metal chromium oxide catalyst includes a copper chromium oxide of the formula Cu x Cr y O z , wherein x is 1 to 2, y is 1 to 2, and z is 4 to 5.
  • Embodiment 13 The method of any of Embodiments 9-12, wherein the deactivated chromium-based catalyst includes a chromium oxide dehydrogenation catalyst manufactured on an alumina support.
  • Embodiment 14 The method of any of Embodiments 9-13, wherein the deactivated chromium-based catalyst includes Cr 2 03 and A1 2 0 3 .
  • Embodiment 15 The method of any of Embodiments 9-14, wherein the dried mixture is calcined at a temperature of 300-600 °C, wherein the metal chromium oxide catalyst is CuCr0 4 .
  • Embodiment 16 The method of Embodiment 9-15, wherein the dried mixture is calcined at a temperature of 600 °C.
  • the invention may alternately comprise, consist of, or consist essentially of, any appropriate components herein disclosed.
  • the invention may additionally, or alternatively, be formulated so as to be devoid, or substantially free, of any components, materials, ingredients, adjuvants or species used in the prior art compositions or that are otherwise not necessary to the achievement of the function and/or objectives of the present invention.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Un procédé de génération de catalyseurs à base d'oxyde de chrome métallique supporté consiste à fournir un catalyseur à base de chrome désactivé; à déterminer la quantité de chrome dans le catalyseur à base de chrome désactivé par spectroscopie d'émission atomique à plasma à couplage inductif; à combiner une quantité calculée d'un matériau métallique avec le catalyseur à base de chrome désactivé pour former un mélange, la quantité calculée étant basée sur la quantité déterminée de chrome dans le catalyseur à base de chrome désactivé afin d'obtenir une stoechiométrie désirée du catalyseur d'oxyde de chrome métallique; à sécher le mélange à une température d'au moins 100 °C; et à calciner le mélange séché à une température d'au moins 250 °C pour former les catalyseurs d'oxyde de chrome métallique.
PCT/IB2017/053712 2016-06-22 2017-06-21 Conversion de catalyseurs à base de chrome désactivé Ceased WO2017221179A1 (fr)

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US201662353094P 2016-06-22 2016-06-22
US62/353,094 2016-06-22

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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4861745A (en) * 1988-08-03 1989-08-29 United Catalyst Inc. High temperature shift catalyst and process for its manufacture

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4861745A (en) * 1988-08-03 1989-08-29 United Catalyst Inc. High temperature shift catalyst and process for its manufacture

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
ACTA CRYST ET AL: "INORGANIC COMPOUNDS The Spinels CuCr204 and CuRh204", NOVEMBER, 1 January 1997 (1997-01-01), pages 657 - 659, XP055406576, Retrieved from the Internet <URL:http://journals.iucr.org/c/issues/1997/06/00/br1169/br1169.pdf> *
CHIEN ET AL: "Effect of heat-treatment conditions on Cu?Cr@c-alumina catalyst for carbon monoxide and propene oxidation", APPLIED CATALYSIS A: GENERAL, ELSEVIER, AMSTERDAM, NL, vol. 131, no. 1, 12 October 1995 (1995-10-12), pages 73 - 87, XP022255260, ISSN: 0926-860X, DOI: 10.1016/0926-860X(95)00136-0 *

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