US20050113614A1 - Catalyst and process for selective hydrogenation - Google Patents

Catalyst and process for selective hydrogenation Download PDF

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US20050113614A1
US20050113614A1 US10720558 US72055803A US2005113614A1 US 20050113614 A1 US20050113614 A1 US 20050113614A1 US 10720558 US10720558 US 10720558 US 72055803 A US72055803 A US 72055803A US 2005113614 A1 US2005113614 A1 US 2005113614A1
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component
catalyst composition
support
metal
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David Lowe
Michel Molinier
John Ou
Michael Risch
Anthony Volpe
Jeffrey Yoder
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ExxonMobil Chemical Patents Inc
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ExxonMobil Chemical Patents Inc
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    • C07C7/00Purification; Separation; Use of additives
    • C07C7/148Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
    • C07C7/163Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56Platinum group metals
    • B01J23/62Platinum group metals with gallium, indium, thallium, germanium, tin or lead
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56Platinum group metals
    • B01J23/63Platinum group metals with rare earths or actinides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56Platinum group metals
    • B01J23/64Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/89Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
    • B01J23/8933Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/896Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with gallium, indium or thallium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/148Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
    • C07C7/163Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation
    • C07C7/167Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation for removal of compounds containing a triple carbon-to-carbon bond
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts 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
    • B01J23/835Catalysts 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 germanium, tin or lead
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
    • C07C2523/54Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
    • C07C2523/56Platinum group metals
    • C07C2523/62Platinum group metals with gallium, indium, thallium, germanium, tin or lead
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
    • C07C2523/825Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36 with gallium, indium or thallium

Abstract

A selective hydrogenation catalyst composition comprises at least two different metal components selected from Groups 8 to 10 of the Periodic Table of Elements, one of which may be rhodium, and at least one metal component selected from Group 13 of the Periodic Table of Elements, such as indium.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • The present application is related by subject matter to U.S. patent application Ser. No. ______, filed Nov. 24, 2003 (Attorney Docket 2003B125) and U.S. patent application Ser. No. ______, filed Nov. 24, 2003 (Attorney Docket 2003B126) filed concurrently herewith, the entire contents of which applications are incorporated herein by reference.
  • FIELD
  • This invention relates to a catalyst and a process for the selective hydrogenation of alkynes and diolefins to olefins.
  • BACKGROUND
  • Light olefins, such as ethylene, propylene and butylenes, can be produced using various processes such as steam cracking, fluid catalytic cracking, conversion of methanol to olefins, paraffin dehydrogenation, alcohol dehydration, methane coupling and Fischer Tropsch reactions. However, these processes often produce varying levels of acetylenic or diene by-products, such as acetylene, methyl acetylene (MA), propadiene (PD), butyne and butadiene. These by-products must be removed from the light olefin streams because they can act as poisons to the downstream processing catalysts, such as polymerization catalysts. The preferred method of removing these by-products is by selective hydrogenation in which, for example, the acetylenes are converted to ethylene, methyl acetylene and propadiene are converted to propylene, and the butyne and butadiene are converted to butylenes.
  • Currently, the commercial catalysts used for this selective hydrogenation comprise nickel or palladium, such as palladium and silver, on an alumina support. However, in addition to producing the desired olefin products, these catalysts tend to generate significant quantities of saturates (for example, ethane, propane and butanes) as a result of over-hydrogenation and green oil (olefin oligomers) as a result of competing oligomerization reactions. Both of these by-products are undesirable in that they reduce the selectivity to the required light olefins. However, the green oil is particularly problematic in that it decreases the life of the hydrogenation catalyst.
  • There is therefore a need for an improved catalyst for the selective hydrogenation of alkynes and diolefins, wherein the catalyst exhibits increased olefin selectivity and reduced selectivity to saturates and oligomers, such as green oil, while retaining high hydrogenation activity.
  • U.S. Patent Application Publication No. 2002/0068843 discloses a catalyst for selectively hydrogenating acetylenic and diolefinic compounds with low green oil formation, the catalyst comprising the following active components loaded on a porous inorganic support: (1) at least one of platinum, palladium, nickel, ruthenium, cobalt, and rhodium; (2) at least one of silver, copper, zinc, potassium, sodium, magnesium, calcium, beryllium, tin, lead, strontium, barium, radium, iron, manganese, zirconium, molybdenum, and germanium; (3) at least one rare earth metal selected from scandium, yttrium and Lanthanides in Group IIIB of Periodic Table of Elements; and (4) bismuth. Preferably, component (1) is platinum or palladium component (2) is silver, potassium or sodium and component (3) is lanthanum or neodymium.
  • U.S. Pat. No. 6,355,854 discloses a method for the oxidative dehydrogenation of an alkane having from 2 to 4 carbon atoms comprising contacting said alkane in the presence of oxygen to a material having the empirical formula
    NixAjBkClOi
    wherein Ni is nickel and x is in the range of about 0.05-0.96; A is a metal selected from the group consisting of cobalt, niobium, tantalum and combinations thereof and j is in the range of from about 0.05-0.8; B is a dopant selected from the group consisting of lithium, sodium, potassium, rubidium, cesium, magnesium, calcium, strontium, barium, manganese, lanthanum, cerium, praseodymium, neodymium, samarium and combinations thereof and k is in the range of from 0-0.5; C is a dopant selected from the group consisting of tin, aluminum, iron, silicon, boron, antimony, titanium, indium, germanium, chromium, lead and combinations thereof and l is in the range of from 0-0.5; i is a number that satisfies the valence requirements of the other elements present; and the sum of j, k and l is at least 0.15.
  • U.S. Pat. No. 6,255,548 discloses a method for selectively hydrogenating a feed comprising an acetylenic compound and/or a diolefin in the presence of a catalyst comprising at least one support, at least one Group VIII metal selected from nickel, palladium, platinum, rhodium, ruthenium and iridium and at least one additional element M selected from germanium, tin, lead, rhenium, gallium, indium, thallium, gold, and silver, wherein the catalyst is formed by introducing said additional element M into an aqueous solvent in the form of at least one water-soluble organometallic compound comprising at least one carbon-M bond. The preferred Group VIII metals are nickel, palladium and platinum and the preferred additional elements M are germanium, tin, gold, and silver.
  • U.S. Pat. No. 5,877,363 discloses a process for the removal of acetylenes and 1,2-butadiene from a C4 aliphatic hydrocarbon stream by contacting the hydrocarbon stream with hydrogen in a distillation column reactor containing a bed of hydrogenation catalyst comprising a Group VIII metal selected from platinum, palladium, rhodium or mixtures thereof; optionally in combination with a Group IB or Group VIB metal, and fractionally distilling the reaction mixture to remove a heavier fraction and removing a fraction overhead comprising substantially all of the C4 compounds having reduced acetylenes and 1,2-butadiene content. The preferred hydrogenation catalyst is palladium.
  • U.S. Pat. Nos. 5,356,851 and 5,364,998 disclose a catalyst and a process for the selective hydrogenation of unsaturated compounds, wherein the catalyst contains 0.1 to 10% of at least one Group VIII metal selected from nickel, palladium, platinum, rhodium and ruthenium and 0.01 to 10% of at least one Group IIIA metal selected from gallium and indium. The molar ratio of Group IIIA metal to Group VIII metal is between 0.2 and 5, preferably between 0.3 and 2. The metals are deposited on a catalyst support by (a) impregnating the support with a solution of a Group IIIA metal compound precursor, then (b) impregnating the product of (a) with a solution of a Group VIII metal compound and then (c) calcining the product of (b) at 110 to 600° C. The preferred Group VIII metals are nickel, palladium and platinum.
  • In U.S. Pat. No. 4,691,070 a catalyst for the hydrogenation of a diolefin is disclosed in which palladium or a compound thereof and at least one co-catalyst component selected from ruthenium, rhodium, cobalt, and rhenium are supported each in the form of an elemental metal or a metal compound on a non-acidic support.
  • A rhodium catalyst is disclosed in U.S. Pat. No. 4,420,420 in which active rhodium metal is supported on a silica type or titania type support, optionally together with one or more co-catalysts including alkaline earth metals, such as calcium, magnesium, barium and the like, noble metals, such as platinum, palladium, iridium, ruthenium, gold and the like, iron, nickel, cobalt, cerium and manganese.
  • Co-pending U.S. patent application Ser. No. ______, filed Nov. 21, 2003 (Attorney Docket 2003B 125), filed concurrently herewith, describes a catalyst and process for selectively hydrogenating alkynes and/or diolefins, wherein the catalyst comprises (a) a rhodium component present in an amount such that the catalyst composition comprises less than 3.0% of rhodium by weight of the total catalyst composition; and (b) an indium component present in an amount such that the catalyst composition comprises at least 0.4% and less than 5.0% of indium by weight of the total catalyst composition.
  • SUMMARY
  • In one aspect, the present invention resides in a catalyst composition comprising at least two metal components selected from Groups 8 to 10 of the Periodic Table of Elements and at least one metal component selected from Group 13 of the Periodic Table of Elements.
  • In one embodiment, one of said at least two metal components selected from Groups 8 to 10 of the Periodic Table of Elements is rhodium. Conveniently, another of said at least two metal components is selected from one or more of iron, ruthenium and cobalt.
  • Conveniently, said at least one metal component selected from Group 13 of the Periodic Table of Elements is indium.
  • In another aspect, the present invention resides in a catalyst composition comprising:
      • (a) a first component comprising rhodium;
      • (b) a second component comprising at least one metal selected from Group 13 of the Periodic Table of Elements; and
      • (c) a third component comprising at least one metal different from said first and second components and selected from Groups 1 to 15 of the Periodic Table of Elements.
  • Conveniently, said second component comprises indium.
  • In one embodiment, said third component comprises at least one metal selected from Groups 8 to 10 of the Periodic Table of Elements and in particular is selected from one or more of iron, ruthenium and cobalt.
  • In yet another aspect, the invention resides in a catalyst composition comprising:
      • (a) a first component comprising rhodium;
      • (b) a second component comprising indium; and
      • (c) a third component selected from one or more of iron, ruthenium and cobalt.
  • In a further aspect, the invention resides in a method of making a catalyst composition, the method comprising:
      • (a) applying a rhodium compound to a support;
      • (b) applying a compound of a metal selected from Group 13 of the Periodic Table of Elements to the support; and
      • (c) applying a compound of a further metal different from rhodium and from said Group 13 metal and selected from Groups 1 to 15 of the Periodic Table of Elements to the support.
  • Conveniently, said further metal compound is applied to the support before either the rhodium compound or the Group 13 metal compound.
  • Conveniently, the Group 13 metal compound is applied to the support either concurrently with or before the rhodium compound.
  • Conveniently, after (a), and/or (b) and/or (c), the support is calcined at a temperature of about 100° C. to about 600° C.
  • In yet a further aspect, the invention resides in use of any of the catalyst compositions described above or more particularly described hereinafter in a process for selectively removing alkynes and/or diolefins, particularly alkynes and/or diolefins having 2 to 4 carbon atoms, from a feedstock containing olefins, particularly C2 to C4 olefins.
  • DETAILED DESCRIPTION OF THE EMBODIMENTS
  • The present invention relates to a novel catalyst composition, its preparation and its use in the hydrogenation of alkynes and diolefins in a feedstock containing other unsaturated compounds, such as olefins. The catalyst composition comprises at least two different metals from Groups 8 to 10 of the Periodic Table of Elements, one of which is typically rhodium, and at least one metal selected from Groups 1 to 15, typically Group 13, of the Periodic Table of Elements, typically indium. The catalyst composition is capable of hydrogenating the alkynes and diolefins in the feedstock with high selectivity to olefins and low selectivity to green oil (oligomers) and saturates. An additional benefit of the present catalyst composition is the extension of catalyst lifetime and/or operating cycle due to the reduction in green oil formation.
  • The Periodic Table of Elements referred to herein is the IUPAC version described in the CRC Handbook of Chemistry and Physics, 78th Edition, CRC Press, Boca Raton, Fla. (1997).
  • As used herein, the term “acetylene” includes the hydrocarbon C2H2 as well as other acetylenic hydrocarbons, such as methyl acetylene (MA). The term “ethylene product stream” includes streams containing the hydrocarbon C2H4 as well as streams containing other mono- and diolefinically unsaturated hydrocarbons. It will be appreciated, however, that while the catalysts are often discussed in terms of selectively hydrogenating acetylene, MA, propadiene (PD) and optionally, butadiene (BD) in a stream that is predominantly ethylene, propylene and/or butylenes, they are not necessarily limited to the treatment of streams that contain ethylene or propylene or butene, but are expected to find applicability to the selective hydrogenation of other unsaturated compounds in streams of other chemical content as well.
  • Catalyst Composition
  • The present catalyst composition comprises three or more metals or metal-based components that may be combined with a binder and/or a support. The term “component” is used to include a metal compound that may not be purely the elemental metal.
  • In one embodiment, the catalyst composition includes:
      • (a) a first component which includes a metal selected from Groups 8 to 10 of the Periodic Table of Elements and normally comprises rhodium;
      • (b) a second component which includes a metal selected from Group 13 of the Periodic Table of Elements and which normally comprises indium; and
      • (c) a third component which also includes a metal selected from Groups 8 to 10 of the Periodic Table of Elements but which is different from the first component metal and normally comprises one or more of iron, cobalt and/or ruthenium.
  • In another embodiment, the catalyst composition includes:
      • (a) a first component comprising rhodium;
      • (d) a second component comprising at least one metal selected from Group 13 of the Periodic Table of Elements; and
      • (c) a third component comprising at least one metal different from said first and second components and selected from Groups 1 to 15 of the Periodic Table of Elements.
  • The catalyst composition conveniently comprises from about 0.01 wt % to about 20 wt %, such as from about 0.04 wt % to about 5 wt %, of the first component. Where the first component is rhodium or a rhodium compound, the catalyst composition typically comprises from about 0.01 wt % to about 10 wt %, such as from about 0.04 wt % to about 5 wt %, of rhodium.
  • The catalyst composition conveniently comprises from about 0.01 wt % to about 30 wt %, such as from about 0.04 wt % to about 20 wt %, of the second component. Where the second component is indium or an indium compound, the catalyst composition typically comprises from about 0.01 wt % to about 20 wt %, such as from about 0.04 wt % to about 10 wt %, of indium.
  • The catalyst composition conveniently comprises from about 0.01 wt % to about 50 wt %, such as from about 0.05 wt % to about 30 wt %, of the third component. Where the third component is iron or an iron compound, the catalyst composition typically comprises from about 0.05 wt % to about 30 wt %, such as from about 0.1 wt % to about 20 wt %, of iron. Where the third component is cobalt or a cobalt compound, the catalyst composition typically comprises from about 0.05 wt % to about 30 wt %, such as from about 0.1 wt % to about 25 wt %, of cobalt. Where the third component is ruthenium or a ruthenium compound, the catalyst composition typically comprises from about 0.05 wt % to about 10 wt %, such as from about 0.1 wt % to about 5 wt %, of ruthenium.
  • All weight percentages for the metal components of the catalyst composition are based on the amount of elemental metal present by weight of the total catalyst composition, including any binder or support.
  • In general, the molar ratio of the first component metal to the second component metal is from about 0.1 to about 1.2, such as from about 0.3 to about 0.9, whereas the molar ratio of the first component metal to the third component metal is about 0.001 to about 0.6, such as about 0.002 to about 0.3.
  • In addition to the active metal components discussed above, the catalyst composition may also include a support or binder material. Suitable support materials comprise carbon, silicon nitride, silicon carbide, boron nitride, magnesium silicate, bentonite, zeolites, metal alloys, zirconia, alumina, silica, silica-alumina, ceria-alumina, aluminates (such as aluminates of Groups 1 and 2 and of the Periodic Table of Elements) and magnesium oxide-silicon oxide mixtures. Preferred support materials include zirconia, alumina and ceria-alumina. The binder or support material conveniently comprises from about 50 wt % to about 99.9 wt %, such as from about 65 wt % to about 99.5 wt %, of the entire catalyst composition.
  • In general, the first, second and third components are present in the catalyst composition in elemental form, but one or more of these components may also be present at least partly in other forms, such as oxide, hydride or sulfide forms.
  • Each of the active metal components may be substantially uniformly distributed throughout the support, can be located within a thin layer at the support surface (commonly referred to as eggshell), can be located at the center of the support (commonly referred to as eggyolk), or can be concentrated between the outer edge and the center of the support (commonly referred to as eggwhite). Preferably, the metal components are concentrated in a thin layer (not more than 1000 microns, conveniently not more than 500 microns, such as not more than 300 microns, for example not more than 100 microns deep) on the surface of the support.
  • Method of Making the Catalyst Composition
  • The catalyst composition can be prepared by a variety of different procedures. One suitable procedure is by impregnation in which a support, such as alumina, is contacted with an aqueous or organic solution of a compound (such as a nitrate, sulfate, halide, formate, acetate, citrate, oxoacetate, oxalate and acetylacetonate) of the chosen metal or metals, the solution volume being less than, equal to or in excess of the retention volume of the support. After maintaining contact between the support and the solution for about 0.01 to about 24 hours, such as about 0.05 to about 4 hours, the impregnated support is dried and normally calcined under air normally at between 100 and 650° C. and preferably between 110 and 600° C. Such a procedure can be used to apply a plurality of active components to the support in a single operation or alternatively separate impregnations can be used to apply the active components successively to the support.
  • Alternatively, the metal components can be applied to the support by mixing a slurry or solution of a compound of the chosen metal or metals with a slurry of a particulate support in a liquid, such as water. After mixing, the resultant slurry may be treated, such as by heating or vacuum drying, to partially or completely remove the liquid, whereafter the treated support may, if necessary, be filtered, then washed with distilled water, dried and calcined as in the case of the impregnation procedure.
  • As a further alternative, the metal components can be applied to the support by precipitation. For example, a liquid solution, such as an aqueous solution, comprising a source of ions of one of the active components can be subjected to conditions sufficient to cause precipitation of the component as a solid from solution, such as by the addition of a precipitating reagent to the solution. Conveniently, the precipitation is conducted at a pH above 7. For example, the precipitating agent may be a base such as sodium hydroxide or ammonium hydroxide.
  • In addition, two or more of the active metal components can be applied to the support simultaneously by co-precipitation. For example, a first liquid solution comprising a source of ions of one of the active components can be combined with a second liquid solution comprising a source of ions of another component. This combination of two solutions can take place under conditions sufficient to cause co-precipitation of both components onto the support from the liquid medium. Alternatively, the source of ions of the one component and the source of ions of the other component may be combined into a single solution. This solution may then be subjected to conditions sufficient to cause co-precipitation of the solid components onto the support, such as by the addition of a precipitating reagent to the solution.
  • Although any compound of the desired metal can be used to apply the different catalyst components to the support, it is found that in the case of rhodium, the preferred compound used to apply the rhodium to the support is rhodium nitrate. In the case of indium, the preferred compounds are indium nitrate and indium formate. In the case of iron, the preferred compounds are iron nitrate and iron ammonium oxalate. In the case of ruthenium, the preferred compound is ruthenium nitrosyl nitrate. In the case of cobalt, the preferred compounds are cobalt nitrate, acetate and formate.
  • In addition, although the different catalyst components can be applied to the support in any order and any combination, in one preferred embodiment, the third catalyst component is added to the support, such as by impregnation, prior to the addition of either or both of the first and second components. Thereafter, the first and second components can be simultaneously added to the support or the second component can be added to the support before the first component.
  • After applying the metal components to the support, the support is normally calcined, such as in air, at between about 100° C. and about 600° C., for example at between about 110° C. and about 500° C. Where the metal components are applied to the support in consecutive steps, a separate calcination step can be conducted after each metal application step or a single calcination step can be conducted after all the metal components have been applied to the support.
  • Finally, the catalyst composition is conveniently heated in a reducing atmosphere, such as an atmosphere containing about 5 to about 30 mol % hydrogen, with the remainder being an inert gas, such as nitrogen, at a temperature of about 100° C. to about 650° C., such as about 200° C. to about 500° C., to further increase the activity of the catalyst. Such a reduction step can be performed in addition to, or in place of, the calcination step(s) referred to above.
  • Selective Hydrogenation Process
  • The catalyst composition of the invention is capable of hydrogenating alkynes and/or diolefins in a feedstock that also contains olefins with high selectivity to olefins and low selectivity to green oil (oligomers formed from two or more alkyne and/or diolefin molecules) and saturates. In particular, when used to selectively hydrogenate C2 to C4 alkynes and/or diolefins in a feedstock also containing C2 to C4 olefins, the present catalyst composition typically achieves an alkyne conversion in excess of 80%, such as in excess of 90%, with an olefin selectivity in excess of 50%, such as in excess of 60%, and a green oil selectivity of less than 10%, such as less than 8%. The reduction in green oil formation should also result in an extension of catalyst lifetime and/or operating cycle.
  • The selective hydrogenation of acetylene, methyl acetylene (MA), propadiene (PD), and/or butadiene (BD) is typically carried out in one of four unit types:
      • (a) Front-End Selective Catalytic Hydrogenation Reactors, where the feed is composed of C3 and lighter hydrocarbons, or C2 and lighter hydrocarbons. In the case of raw gas applications, other components such as butadiene, ethyl acetylene, dimethyl acetylene, vinyl acetylene, cyclopentadiene, benzene, and toluene can also be present.
      • (b) Back-End Selective Catalytic Hydrogenation Reactors, where the feed is composed of an ethylene-rich stream.
      • (c) MAPD Selective Catalytic Hydrogenation Reactors, where the feed is composed of a propylene-rich stream.
      • (d) BD Selective Catalytic Hydrogenation Reactors, where the feed is composed of a butylene-rich stream.
  • The operating parameters of an alkyne/alkadiene selective hydrogenation process are not narrowly critical and can controlled in view of a number of interrelated factors including, but not necessarily limited to, the chemical composition of the feedstock, the control systems and design of a particular plant, etc (i.e. different reactor configurations including front-end, tail-end, MAPD, and BD converters as mentioned briefly above). In general, however, suitable operating parameters include a temperature of from about 20° C. to about 150° C., such as from about 30° C. to about 100° C., a pressure of from about 100 psig to about 580 psig (690 kPa to 4100 kPa), such as from about 200 psig to about 440 psig (1400 kPa to 3400 kPa), a H2/C2H2 molar feed ratio of from about 1 to about 1000, such-as of from about 1.1 to about 800 and, assuming the reaction is in the vapor phase, a GHSV from about 100 to about 20,000, such as from about 500 to about 15,000 or, if the reaction is in the liquid phase, an LHSV of 0.1 to 100, such as from 1 to 25.
  • The following descriptions serve to illustrate how the inventive process may be practiced in the different commercial units.
  • In the case of a front-end (FE) selective hydrogenation reactor, the inlet operating temperature may range from about 30 to about 150° C., such as from about 50 to about 100° C. Representative operating pressures may range from about 100 psig to about 500 psig (about 690 to 3,500 kPa), such as from about 200 psig to about 400 psig (about 1400 to 2800 kPa). The GHSV may range from about 5000 to about 20,000, such as from about 8000 to about 15,000. Further, the H2 partial pressure may range from about 25 psig to about 175 psig (about 172 to 1200 kPa), such as from about 50 psig to about 140 psig (about 345 to 965 kPa). The feedstreams in FE selective hydrogenation processes typically contain at least about 20% ethylene, and less than 1% acetylene, with the balance comprising ethane, methane, hydrogen and small amounts of similarly light components. (All percentages are mole % unless otherwise noted). Depending upon the process configuration of the plant, this feed stream can also contain C3 components such as methyl acetylene, propadiene, propylene, and propane. Still heavier components such as 1,3 butadiene; 1,2 butadiene; ethyl acetylene; dimethyl acetylene; vinyl acetylene; cyclopentadiene; benzene; toluene and mixtures thereof may also be present as a result of certain process configurations.
  • In the case of a back-end selective hydrogenation reactor, the inlet operating temperature may range from about 30 to about 150° C., such as from about 40 to about 90° C. Representative operating pressures may range from about 100 psig to about 500 psig (about 690 to 3,500 kPa), such as from about 200 psig to about 400 psig (about 1400 to 2800 kPa). The GHSV may range from about 1000 to about 10,000, such as from about 3000 to about 8000. Further, the H2/C2H2 molar feed ratio may range from about 0.5 to about 20, such as from about 1.0 to about 1.5. The feedstreams in back-end selective hydrogenation processes in may contain about 2% acetylene, about 70% ethylene, and the balance other C2 compounds.
  • In the case of a methyl acetylene/propadiene (MAPD) selective hydrogenation reactor, operation can be conducted in either the liquid or vapor phase. In the case of liquid phase operation, the inlet operating temperature may range from about 20 to about 100° C., such as from about 30 to about 80° C. Representative operating pressures may range from about 150 psig to about 600 psig (about 1000 to 4100 kPa), such as from about 250 psig to about 500 psig (about 1700 to 3400 kPa). The LHSV may range from about 0.1 to about 100, such as from about 1 to about 10. In the case of the vapor phase operation, the inlet operating temperature may range from about 20 to about 600° C., such as from about 200 to about 400° C. Representative operating pressures may range from about 150 psig to about 600 psig (about 1000 to 4100 kPa), such as from about 250 psig to about 500 psig (about 1700 to 3400 kPa). The GHSV may range from about 100 to about 20,000, such as from about 500 to about 5000. Further, the H2/C2H2 molar feed ratio may range from about 0.5 to about 20, such as from about 1 to about 10. The feedstreams in MAPD selective hydrogenation processes may contain at least 80% propylene, and less than 10% of a compound selected from the group consisting of methyl acetylene, propadiene, and mixtures thereof.
  • In the case of a butadiene (BD) selective hydrogenation reactor, operation can be conducted in either the liquid or vapor phase. In the case of liquid phase operation, the inlet operating temperature may range from about 20 to about 120° C., such as from about 40 to about 100° C. Representative operating pressures may range from about 150 psig to about 600 psig (about 1000 to 4100 kPa), such as from about 200 psig to about 400 psig (about 1400 to 2800 kPa). The LHSV may range from about 0.1 to about 100, such as from about 1 to about 25. In the case of the vapor phase operation, the inlet operating temperature may range from about 20 to about 600° C., such as from about 50 to about 200° C. Representative operating pressures may range from about 150 psig to about 600 psig (about 1000 to 4100 kPa), such as from about 250 psig to about 500 psig (about 1700 to 3400 kPa). The GHSV may range from about 100 to about 20,000, such as from about 500 to about 5000. Further, the H2/C2H2 molar feed ratio may range from about 0.5 to about 20, preferably from about 1 to about 10. The feedstreams in BD selective hydrogenation processes may contain at least 90% butylene, and greater than 0.2% butadiene.
  • The invention will now be more particularly described with reference to the following Examples.
  • In the Examples, the following definitions are employed: C 2 H 2 Conversion: ( C 2 H 2 ) i n - ( C 2 H 2 ) out ( C 2 H 2 ) i n × 100 C 2 H 4 ( Gain ) Selectivity: ( C 2 H 2 ) i n - ( C 2 H 2 ) out - C 2 H 6 produced - ( 2 × C 4 produced + 3 × C 6 produced ) ( C 2 H 2 ) i n - ( C 2 H 2 ) out × 100 C 2 H 6 Selectivity: C 2 H 6 produced ( C 2 H 2 ) i n - ( C 2 H 2 ) out × 100 Green-Oil   Selectivity: ( 2 × C 4 produced + 3 × C 6 produced ) ( C 2 H 2 ) i n - ( C 2 H 2 ) out × 100
  • EXAMPLE 1 (COMPARATIVE) Pd—Ag Catalyst
  • This example illustrates the performance of a current state of the art commercial Pd-based catalyst. The catalyst, G-58C, was obtained from Sud-Chemie, Inc. and comprised 0.03 wt % Pd and 0.18 wt % Ag on alumina. The catalyst was prereduced at 120° C. for 2 hours under a 100% hydrogen atmosphere and was then evaluated under the following conditions: temperature=100° C., pressure=300 psig, GHSV=4500, H2/C2H2 feed ratio=1.1. The hydrocarbon feed contained nominally 1.65 mole % acetylene and 70 mole % ethylene, with balance being nitrogen. Impurities that may be present in the feed include carbon monoxide (<0.5 ppm), mercury, arsine, phosphorus (<5 ppb), sulfur (<1 ppm), oxygen (<1 ppm), water (<10 ppm), acetone (<10 ppm) and methanol (<2 ppm). Test results at 100% hydrogen conversion are given in Table 1 below.
    TABLE 1
    Green
    Catalyst (wt %) C2H2 conv (%) C2H4 select (%) Oil select (%)
    0.03% Pd/0.18% Ag 84.8 60.1 24.6
  • It will be seen that the conventional catalyst had an ethylene selectivity of about 60% but its green oil selectivity was almost 25%.
  • EXAMPLE 2 (COMPARATIVE) Rh—In Bimetallic Catalyst
  • A rhodium/indium bimetallic catalyst of the type described in our co-pending U.S. patent application Ser. No. ______, filed Nov. 24, 2003 (Attorney Docket 2003B 125), filed concurrently herewith, was prepared and tested as follows.
  • 10 g of theta-alumina (SBa-90 supplied by Sasol) were mixed with 50 ml of deionized water to form a slurry. Then 0.189 gm Rh(NO3)3.2H2O was dissolved in 80 ml deionized water and was mixed with 0.314 g In(NO3)3.xH2O dissolved in 50 ml deionized water. The solution containing both metals was added to the alumina slurry and, after 1 hour stirring, the slurry was gently heated until most of the water was removed. The resulting paste was dried in a vacuum oven for 2 hours at 100° C., whereafter the remaining powder was calcined in air for 2 hours at 120° C. and then for 4 hours at 450° C. The resultant catalyst composition was then reduced at 350° C. for 5 hours in a nitrogen atmosphere containing 5 mol % hydrogen.
  • The final catalyst contained 0.6 wt % rhodium and 1.2 wt % indium and had a rhodium to indium molar ratio of 0.5. When the catalyst was used to treat the same hydrocarbon feed under the same conditions as Example 1, the results shown in Table 2 were obtained. Table 2 also gives the results obtained with the catalyst of Example 1 (but with the prereduction regime of Example 2) after the same time on stream (TOS).
    TABLE 2
    C2H6
    Catalyst TOS C2H2 conv C2H4 select select Green Oil
    (wt %) (hrs) (%) (%) (%) select (%)
    0.6% Rh/1.2% In 11 80.5 40.6 51.7 7.7
    0.03% Pd/0.18% Ag 11 93.2 50.8 24.8 24.5
  • It will be seen that the green oil selectivity of the Example 2 catalyst was less than one third of that of the catalyst of Example 1.
  • EXAMPLE 3 Rh—In-Metal Trimetallic Catalysts
  • A series of trimetallic catalysts were prepared each containing 0.6 wt % rhodium, 1.2 wt % indium and 0.6 wt % of a third metal selected from Groups 2 to 15 of the Periodic Table of Elements on an alumina support. In each case, the alumina support was Norton SA6175 alumina which had been heat treated at 975° C. for 15 minutes to convert the gamma phase alumina to the theta phase.
  • Each catalyst was prepared as follows. Rhodium nitrate (10.01 wt % solution) obtained from Strem Chemicals was diluted to 2.50 wt % rhodium with deionized water. Solid indium nitrate trihydrate obtained from Prochem was dissolved to 6.56 wt % indium using deionized water. 169.1 μL of the diluted rhodium nitrate solution and 117.7 μL of the prepared indium nitrate solution were mixed with deionized water (313.1 μL). This mixed rhodium-indium solution (120 μL) was added to 148 mg of alumina in a vial and agitated by vibration for 30 minutes at room temperature. The obtained material was dried at 120° C. for 3 hours and then calcined in air at 450° C. for 4 hours to afford a sample containing 0.6 wt % rhodium and 1.2 wt % indium supported on theta alumina. Separately prepared calcined samples were then used as the starting materials for the second impregnation steps for each catalyst as described below.
  • 0.6% Scandium: Scandium nitrate solution was prepared by dissolving solid scandium nitrate hydrate as obtained from Aldrich to 4.53 wt % metal using deionized water. The prepared scandium nitrate solution (189.7 μL) was mixed with deionized water (1250.3 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Yttrium: Yttrium nitrate solution was prepared by dissolving solid yttrium nitrate hydrate as obtained from Aldrich to 9.63 wt % metal using deionized water. The prepared yttrium nitrate solution (85.8 μL) was mixed with deionized water (1354.2 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Lanthanum: Lanthanum nitrate solution was prepared by dissolving solid lanthanum nitrate hydrate as obtained from Aldrich to 12.68 wt % metal using deionized water. The prepared lanthanum nitrate solution (64.2 μL) was mixed with deionized water (1375.8 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Titanium: Ammonium titanyl oxalate solution was prepared by dissolving solid ammonium titanyl oxalate hydrate as obtained from Aldrich to 4.61 wt % metal in deionized water. The prepared ammonium titanyl oxalate solution (195.9 μL) was mixed with deionized water (1244.1 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% zirconium: Zirconyl nitrate solution was prepared by diluting the as received zirconyl nitrate solution as obtained from Aldrich as a solution in dilute nitric acid to 14.6 wt % metal using deionized water. The prepared zirconyl nitrate solution (50.3 μL) was mixed with deionized water (1389.7 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Hafnium: Hafnium acetylacetonate solution was prepared by mixing solid hafnium acetylacetonate as obtained from Strem Chemicals with deionized water and nitric acid. The mixture was heated to 60° C. until homogeneous. The final concentrations were 7.57 wt % hafnium and 5.3 wt % nitric acid. The prepared hafnium acetylacetonate solution (129.1 μL) was mixed with deionized water (1310.9 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Vanadium: Solid vanadium pentoxide as obtained from Aldrich was mixed with 1 M solution of oxalic acid in deionized water and the resultant mixture was diluted with deionized water to the desired concentration. The mixture was heated until a deep blue color was achieved and the solution became homogeneous. The resultant vanadium oxalate solution (6.88 wt % vanadium, 131.3 μL) was mixed with deionized water (1308.7 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Niobium: Niobium oxalate solution was prepared by dissolving solid ammonium niobium oxalate as obtained from Aldrich to 4.647 wt % metal in deionized water. The prepared niobium oxalate solution (202.9 μL) was mixed with deionized water (1237.1 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Tantalum: Tantalum (V) ethoxide as obtained from Aldrich was mixed with a 1 M solution of oxalic acid in deionized water and the resultant mixture was heated at 60° C. until homogeneous. The resultant tantalum oxalate solution (9.0 wt % tantalum, 102.1 μL) was mixed with deionized water (1337.9 μL) and the diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Molybdenum: Molybdenum trioxide as obtained from Aldrich was mixed with a 1 M solution of oxalic acid in deionized water and the resultant mixture was heated to 60° C. until homogeneous. The resultant molybdenum oxalate solution (5.50 wt % molybdenum, 171.5 μL) was mixed with deionized water (1268.5 μL) and the diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Tungsten: Ammonium metatungstate solution was prepared by dissolving solid ammonium metatungstate hydrate as obtained from Aldrich in deionized water to 10.91 wt % metal. The prepared ammonium metatungstate solution (84.9 μL) was mixed with deionized water (1355.1 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Manganese: Manganese nitrate solution was prepared by dissolving solid manganese (II) nitrate hydrate as obtained from Aldrich to 9.46 wt % metal using deionized water. The prepared manganese nitrate solution (87.3 μL) was mixed with deionized water (1352.7 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Rhenium: A perrhenic acid solution was prepared by diluting the perrhenic acid solution as received from Aldrich to 4.986 wt % metal using deionized water. The prepared perrhenic acid solution (201.6 μL) was mixed with deionized water (1238.4 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Iron: Ferric nitrate solution was prepared by dissolving solid iron (III) nitrate hydrate as obtained from Aldrich to 3.42 wt % metal using deionized water. The prepared iron nitrate solution (275.7 μL) was mixed with deionized water (1164.3 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Ruthenium: Ruthenium nitrosyl nitrate solution was prepared by dissolving solid ruthenium nitrosyl nitrate hydrate as obtained from Alfa Aesar to 3.49 wt % metal using deionized water. The prepared ruthenium nitrosyl nitrate solution (282.7 μL) was mixed with deionized water (1157.3 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Cobalt: Cobalt nitrate solution was prepared by dissolving solid cobalt (II) nitrate hydrate as obtained from Alfa Aesar to 5.21 wt % metal using deionized water. The prepared cobalt nitrate solution (181.0 μL) was mixed with deionized water (1259.0 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Nickel: Nickel nitrate solution was prepared by dissolving solid nickel (II) nitrate hydrate as obtained from Alfa Aesar to 3.527 wt % metal using deionized water. The prepared nickel nitrate solution (272.2 μL) was mixed with deionized water (1167.8 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Copper: Copper nitrate solution was prepared by dissolving solid copper nitrate (II) hydrate as obtained from Aldrich to 3.51 wt % metal using deionized water. The prepared copper nitrate solution (278.5 μL) was mixed with deionized water (1161.5 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Gold: Hydrogen tetrachloroaurate solution was prepared by dissolving solid hydrogen tetrachloroaurate (III) hydrate as obtained from Aldrich to 3.37 wt % metal using deionized water. The prepared tetrachloroaurate solution (301.1 μL) was mixed with deionized water (1138.9 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Zinc: Zinc nitrate solution was prepared by dissolving solid zinc nitrate hydrate as obtained from Aldrich to 3.51 wt % metal using deionized water. The prepared zinc nitrate solution (276.0 μL) was mixed with deionized water (1164.0 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Gallium: Gallium nitrate solution was prepared by dissolving solid gallium (III) nitrate hydrate as obtained from Aldrich to 7.41 wt % metal using deionized water. The prepared gallium nitrate solution (116.0 μL) was mixed with deionized water (1324.0 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Iridium: Hydrogen hexachloroiridate solution was prepared by dissolving hydrogen hexachloroiridate (IV) hydrate as obtained from Aldrich to 8.08% metal using deionized water. The prepared hexachloroiridate solution (115.7 μL) was mixed with deionized water (1324.3 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Germanium: A concentrated solution of tetramethylammonium hydroxide was prepared in deionized water and solid germanium (IV) oxide as obtained from Aldrich was mixed with this solution and agitated until homogeneous. The prepared germanium oxide solution had concentrations of 9.526 wt % germanium and 15.0 wt % tetramethylammonium hydroxide. This solution (97.3 μL) was mixed with deionized water (1342.7 μL). The diluted germanium solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Tin: A concentrated solution of tetramethylammonium hydroxide was prepared in deionized water and solid tin tartrate, as obtained from Sigma and maintained at 0° C. until used, was mixed with this solution and agitated until homogeneous. The prepared tin solution had concentrations of 4.892 wt % tin and 22.7 wt % tetramethylammonium hydroxide. This solution (201.7 μL) was mixed with deionized water (1238.3 μL). The diluted tin solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Antimony: Antimony oxalate solution was prepared by mixing antimony (III) acetate as obtained from Aldrich with a 1 M solution of oxalic acid in deionized water and heating the mixture to 60° C. A concentrated solution of ammonium hydroxide in deionized water was added dropwise to the antimony containing mixture until the solution became homogeneous. At this point, the solution was diluted as-required with oxalic acid solution or deionized water to desired metal concentration. The prepared antimony oxalate solution (3.3% antimony, 290.9 μL) was mixed with deionized water (1149.1 μL) and the resultant diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Bismuth: Bismuth nitrate solution was prepared by dissolving solid bismuth (III) nitrate hydrate as obtained from Aldrich to 7.49 wt % metal in a mixture of nitric acid and deionized water such that the final concentration of nitric acid was 12.7 wt %. The prepared bismuth nitrate solution (115.7 μL) was mixed with deionized water (1324.3 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Cerium: Ammonium cerium nitrate solution was prepared by dissolving solid ammonium cerium (IV) nitrate hydrate as obtained from Aldrich to 10.03 wt % metal using deionized water. The prepared ammonium cerium nitrate solution (80.5 μL) was mixed with deionized water (1359.5 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Praseodymium: Praseodymium nitrate solution was prepared by dissolving solid praseodymium nitrate hydrate as obtained from Aldrich to 12.74 wt % metal using deionized water. The prepared praseodymium nitrate solution (64.3 μL) was mixed with deionized water (1375.7 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Neodymium: Neodymium nitrate solution was prepared by dissolving solid neodymium (III) nitrate hydrate as obtained from Aldrich to 10.9 wt % metal using deionized water. The prepared neodymium nitrate solution (78.2 μL) was mixed with deionized water (1361.8 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Samarium: Samarium nitrate solution was prepared by dissolving solid samarium (III) nitrate hydrate as obtained from Aldrich to 11.5 wt % metal using deionized water. The prepared samarium nitrate solution (73.5 μL) was mixed with deionized water (1366.5 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Europium: Europium nitrate solution was prepared by dissolving solid europium (III) nitrate hydrate as obtained from Aldrich to 14.73 wt % metal using deionized water. The prepared europium nitrate solution (53.2 μL) was mixed with deionized water (1386.8 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Gadolinium: Gadolinium nitrate solution was prepared by dissolving solid gadolinium (III) nitrate hydrate as obtained from Aldrich to 11.26 wt % metal using deionized water. The prepared gadolinium nitrate solution (75.1 μL) was mixed with deionized water (1364.9 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Terbium: Terbium nitrate solution was prepared by dissolving solid terbium (III) nitrate hydrate as obtained from Aldrich to 12.55 wt % metal using deionized water. The prepared terbium nitrate solution (65.8 μL) was mixed with deionized water (1374.2 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Dysprosium: Dysprosium nitrate solution was prepared by dissolving solid dysprosium (III) nitrate hydrate as obtained from Aldrich to 11.58 wt % metal using deionized water. The prepared dysprosium nitrate solution (73.0 μL) was mixed with deionized water (1367.0 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for, 4 hours.
  • 0.6% Holmium: Holmium nitrate solution was prepared by dissolving solid holmium (III) nitrate hydrate to 10.59 wt % metal using deionized water. The prepared holmium nitrate solution (81.8 μL) was mixed with deionized water (1358.2 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Erbium: Erbium nitrate solution was prepared by dissolving solid erbium (III) nitrate hydrate as obtained from Aldrich to 10.87 wt % metal using deionized water. The prepared erbium nitrate solution (78.4 μL) was mixed with deionized water (1361.6 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Ytterbium: Ytterbium nitrate solution was prepared by dissolving solid ytterbium (III) nitrate hydrate as obtained from Aldrich to 11.31 wt % metal using deionized water. The prepared ytterbium nitrate solution (76.0 μL) was mixed with deionized water (1364.0 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Magnesium: Magnesium acetate solution was prepared by dissolving solid magnesium acetate hydrate as obtained from Aldrich to 5.83 wt % metal using deionized water. The prepared magnesium acetate solution (151.1 μL) was mixed with deionized water (1288.9 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 0.120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Calcium: Calcium acetate solution was prepared by dissolving solid calcium acetate hydrate as obtained from Aldrich to 5.9 wt % using deionized water. The prepared-calcium acetate solution (158.4 μL) was mixed with deionized water (1281.6 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • 0.6% Strontium: Strontium formate solution was prepared by dissolving solid strontium formate as obtained from Pfaltz and Bauer to 5.73 wt % metal using deionized water. The prepared strontium formate solution (169.1 μL) was mixed with deionized water (1270.9 μL). This diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • This series of catalysts was used to treat the same hydrocarbon feed under the same conditions as Example 1 with the exception that the prereduction step was carried out at 350° C. for 2.5 hours in a nitrogen atmosphere containing 5% hydrogen. The results summarized in Table 3 were obtained.
    TABLE 3
    C2H2
    conv C2H4 select Green Oil
    Catalyst (wt %) TOS (%) (%) select (%)
    0.6% Rh, 1.2% In, 0.6% Sc 9.9 63.9 59.9 6.5
    0.6% Rh, 1.2% In, 0.6% Y 9.9 62.2 61.3 6.3
    0.6% Rh, 1.2% In, 0.6% La 9.9 66.7 58.8 7.3
    0.6% Rh, 1.2% In, 0.6% Ti 9.9 58.3 62.9 5.8
    0.6% Rh, 1.2% In, 0.6% Zr 9.9 48.9 60.6 6.5
    0.6% Rh, 1.2% In, 0.6% Hf 9.9 62.9 60.8 7.2
    0.6% Rh, 1.2% In, 0.6% V 10.4 72.6 62.6 6.0
    0.6% Rh, 1.2% In, 0.6% Nb 10.4 57.1 58.2 6.9
    0.6% Rh, 1.2% In, 0.6% Ta 10.4 72.2 58.2 7.0
    0.6% Rh, 1.2% In, 0.6% Mo 10.4 58.8 65.8 5.8
    0.6% Rh, 1.2% In, 0.6% W 10.4 46.8 65.0 6.3
    0.6% Rh, 1.2% In, 0.6% Mn 10.4 71.0 60.6 7.2
    0.6% Rh, 1.2% In, 0.6% Re 11.0 80.4 65.9 5.4
    0.6% Rh, 1.2% In, 0.6% Fe 11.0 73.8 65.3 6.1
    0.6% Rh, 1.2% In, 0.6% Ru 11.0 83.8 64.1 6.7
    0.6% Rh, 1.2% In, 0.6% Co 11.0 69.9 65.1 5.6
    0.6% Rh, 1.2% In, 0.6% Ni 11.5 75.5 62.0 6.0
    0.6% Rh, 1.2% In, 0.6% Cu 11.5 30.2 55.0 9.2
    0.6% Rh, 1.2% In, 0.6% Au 11.5 30.7 12.5 12.0
    0.6% Rh, 1.2% In, 0.6% Zn 11.5 67.5 66.1 5.2
    0.6% Rh, 1.2% In, 0.6% Ga 11.5 52.7 64.8 6.2
    0.6% Rh, 1.2% In, 0.6% Ir 11.5 26.7 46.2 18.3
    0.6% Rh, 1.2% In, 0.6% Ge 12.0 70.8 64.4 5.9
    0.6% Rh, 1.2% In, 0.6% Sn 12.0 59.8 59.2 6.8
    0.6% Rh, 1.2% In, 0.6% Sb 12.0 45.5 49.4 8.4
    0.6% Rh, 1.2% In, 0.6% Bi 12.0 27.8 62.0 6.2
    0.6% Rh, 1.2% In, 0.6% Ce 12.0 59.8 57.6 7.4
    0.6% Rh, 1.2% In, 0.6% Pr 12.0 66.5 58.9 7.8
    0.6% Rh, 1.2% In, 0.6% Nd 12.5 72.3 61.5 6.2
    0.6% Rh, 1.2% In, 0.6% Sm 12.5 66.1 59.2 5.6
    0.6% Rh, 1.2% In, 0.6% Eu 12.5 75.9 61.2 6.8
    0.6% Rh, 1.2% In, 0.6% Gd 12.5 58.7 60.9 5.6
    0.6% Rh, 1.2% In, 0.6% Tb 12.5 60.4 63.4 5.7
    0.6% Rh, 1.2% In, 0.6% Dy 12.5 73.7 60.9 6.6
    0.6% Rh, 1.2% In, 0.6% Ho 13.0 73.8 62.9 6.0
    0.6% Rh, 1.2% In, 0.6% Er 13.0 62.7 61.2 5.9
    0.6% Rh, 1.2% In, 0.6% Yb 13.0 76.3 59.2 6.9
    0.6% Rh, 1.2% In, 0.6% Mg 13.0 59.3 63.5 5.5
    0.6% Rh, 1.2% In, 0.6% Ca 13.0 49.3 66.5 6.0
    0.6% Rh, 1.2% In, 0.6% Sr 13.0 72.6 62.8 6.2
  • It will be seen that a majority of the trimetallic catalysts of Example 3 had a higher ethylene selectivity, and all had a lower green oil selectivity, than the catalyst of Example 1.
  • EXAMPLE 4 Rh—In—Ru Trimetallic Catalyst
  • A series of trimetallic catalysts containing rhodium, indium and ruthenium supported on alumina were produced in the same way as in Example 3 but with the relative amounts of the metals being varied and the prereduction step being conducted at 450° C. for 5 hours in a nitrogen atmosphere containing 5 mol % hydrogen.
  • When the catalysts were used to treat the same hydrocarbon feed under the same conditions as Example 1, the results summarized in Table 4 were obtained.
    TABLE 4
    C2H2
    conv C2H4 select Green Oil
    Catalyst (wt %) TOS (%) (%) select (%)
    0.6% Rh, 0.6% In, 0.3% Ru 10.6 90.6 66.6 5.3
    0.6% Rh, 1.2% In, 0.3% Ru 10.6 79.8 72.7 4.9
    0.6% Rh, 0.6% In, 1% Ru 11.1 93.8 68.0 5.1
    0.6% Rh, 1.2% In, 1% Ru 11.1 81.5 73.7 5.2
    0.6% Rh, 1.8% In, 1% Ru 11.1 65.1 65.8 8.5
    0.6% Rh, 0.6% In, 1.7% Ru 11.6 92.5 67.5 5.4
    0.6% Rh, 1.2% In, 1.7% Ru 11.6 76.8 73.2 5.2
    0.6% Rh, 1.8% In, 1.7% Ru 11.6 63.7 67.7 6.4
    0.6% Rh, 0.6% In, 2.4% Ru 12.2 92.1 67.5 5.4
    0.6% Rh, 1.2% In, 2.4% Ru 12.2 80.8 72.3 5.3
    0.6% Rh, 1.8% In, 2.4% Ru 12.2 62.8 67.0 6.2
  • It will be seen from Table 4 that the use of a trimetallic Rh-In-Ru catalyst allows a high ethylene selectivity (65-74%) and a low green oil selectivity (5-8%) to be achieved at a high acetylene conversion (90% or more).
  • EXAMPLE 5 Rh—In—Fe Trimetallic Catalyst
  • A series of trimetallic catalysts containing 0.6 wt % rhodium, 1.2 wt % indium and varying amounts of iron supported on alumina were produced in the same way as in Example 3 but with the order of addition of the metals to the alumina support being varied as follows:
      • (a) co-impregnation of Rh/In/Fe with the alumina;
      • (b) impregnation of Fe followed by co-impregnation of Rh/In; and
      • (c) co-impregnation of Rh/In followed by impregnation of Fe.
        Again, the prereduction step was conducted at 450° C. for 5 hours in a nitrogen atmosphere containing 5 mol % hydrogen.
  • When the catalysts were used to treat the same hydrocarbon feed under the same conditions as Example 1, the results summarized in Table 5 were obtained.
    TABLE 5
    Metal C2H2 conv C2H4 select Green Oil
    Fe (wt %) Addition TOS (%) (%) select (%)
    0.6 (c) 10.1 99.4 74.3 5.9
    0.6 (a) 10.1 90.0 70.7 8.4
    2.2 (c) 10.7 97.1 72.2 5.7
    2.2 (b) 10.7 99.4 74.8 5.9
    1.75 (a) 10.7 98.7 71.5 7.9
    3.7 (c) 11.2 99.9 73.0 6.4
    3.7 (b) 11.2 99.8 73.9 6.2
    2.9 (a) 11.2 99.6 71.4 8.0
    5.3 (c) 11.8 99.9 72.9 6.4
    5.3 (b) 11.8 99.9 73.5 6.3
    4.1 (a) 11.8 99.8 70.5 8.3
    6.9 (c) 12.3 99.9 72.8 6.3
    6.9 (b) 12.3 99.9 73.7 6.2
    5.2 (a) 12.3 99.8 71.1 7.9
    8.4 (c) 12.9 99.9 71.8 6.7
    8.4 (b) 12.9 99.9 73.8 6.2
    6.4 (a) 12.9 99.6 70.6 8.0
    10 (c) 13.4 95.7 73.3 6.4
    10 (b) 13.4 99.9 73.5 6.2
    7.5 (a) 13.4 99.8 70.0 8.4
  • It will be seen from Table 5 that the use of a trimetallic Rh-In-Fe catalyst allows a high ethylene selectivity (>70%) and a low green oil selectivity (6-9%) to be achieved at a high acetylene conversion (90-100%).
  • EXAMPLE 6 Rh—In—Fe Trimetallic Catalysts with low Rh Loading
  • A series of trimetallic catalysts containing 0.2 wt % rhodium, 7 wt % iron and varying amounts of indium supported on alumina were produced in the same way as in Example 3, with the iron being impregnated first, and followed by a simultaneous impregnation of rhodium and indium. Again, the prereduction step was conducted at 450° C. for 5 hours in a nitrogen atmosphere containing 5 mol % hydrogen.
  • When the catalysts were used to treat the same hydrocarbon feed under the same conditions as Example 1, the results summarized in Table 6 were obtained.
    TABLE 6
    C2H2 conv C2H4 select Green Oil
    Catalyst (wt %) TOS (%) (%) select (%)
    0.2% Rh, 0.4% In, 7% Fe 16.0 100.0 73.8 7.2
    0.2% Rh, 0.5% In, 7% Fe 16.5 99.3 73.6 6.5
    0.2% Rh, 0.3% In, 7% Fe 15.5 99.2 72.5 7.4
    0.2% Rh, 0.6% In, 7% Fe 17.1 99.1 71.8 6.5
    0.2% Rh, 0.2% In, 7% Fe 14.9 97.8 70.5 8.0
  • It will be seen from Table 6 that with the Rh-In-Fe catalyst system, very high acetylene conversion activity and good selectivities can be achieved even at low rhodium loadings.
  • EXAMPLE 7 Rh—In—Co Trimetallic Catalyst
  • A series of catalysts containing 0.3 wt % rhodium and varying amounts of indium and cobalt supported on alumina were produced by incipient wetness impregnation of the alumina with a cobalt nitrate solution and then with a solution containing rhodium and indium nitrates. After each impregnation step the catalyst precursor was calcined for 4 hours in air according to one of the following regimes:
    • (a) calcine at 550° C. after Co addition and at 550° C. after Rh/In addition;
    • (b) calcine at 550° C. after Co addition and at 450° C. after Rh/In addition;
    • (c) calcine at 450° C. after Co addition and at 550° C. after Rh/In addition;
    • (d) calcine at 450° C. after Co addition and at 450° C. after Rh/In addition;
      Again, a prereduction step was conducted at 450° C. for 5 hours in a nitrogen atmosphere containing 5 mol % hydrogen.
  • When the catalysts were used to treat the same hydrocarbon feed under the same conditions as Example 1, the results summarized in Table 7 were obtained.
    TABLE 7
    C2H2 C2H4
    conv select Green Oil
    Catalyst (wt %) Calc. TOS (%) (%) select (%)
    0.3% Rh, 1.2% In, 9% Co (a) 12.7 97.5 70.8 7.5
    0.6% Rh, 1.6% In, 5% Co (b) 13.2 96.2 68.5 6.6
    0.3% Rh, 1.2% In, 9% Co (b) 11.1 95.2 69.4 6.9
    0.3% Rh, 0.8% In, 9% Co (c) 12.7 94.4 67.4 8.4
    0.3% Rh, 1.2% In, 4.9% Co (a) 12.2 94.2 70.5 6.6
    0.3% Rh, 0.8% In, 9% Co (d) 11.1 94.2 67.7 7.7
    0.3% Rh, 1.2% In, 9% Co (d) 11.1 93.8 66.7 8.2
    0.3% Rh, 0.8% In, 4.9% Co (c) 12.2 92.8 68.1 6.6
    0.3% Rh, 1.2% In, 9% Co (c) 12.7 92.6 65.7 9.2
  • It will be seen from Table 7 that a high acetylene conversion activity together with good selectivities to ethylene and green oil can also be achieved with a trimetallic Rh—In—Co catalyst.
  • EXAMPLE 8 Pt—In—Ni Catalyst
  • A catalyst containing platinum, indium and nickel was prepared in the following manner.
  • A solution of tetraammineplatinum nitrate was prepared by dissolving solid tetraammineplatinum nitrate as obtained from Aldrich to 3.5 wt % platinum using deionized water. A solution of indium nitrate was prepared by dissolving solid indium nitrate as obtained from Prochem to 11.05 wt % indium using deionized water. A solution of nickel nitrate was prepared by dissolving solid nickel nitrate as obtained from Alfa Aesar to 13.24 wt % nickel using deionized water. An impregnation solution was then prepared by mixing the prepared platinum solution (73.9 μL), the prepared indium solution (311.5 μL) and the prepared nickel solution (226.6 μL) with deionized water (108.0 μL). This impregnation solution (120 μL) was then added to 148 mg of Norton SA6175 alumina, which had been heat treated at 975° C. for 15 minutes to convert gamma phase to theta phase, and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.
  • The catalyst was used to treat the same hydrocarbon feed under the same conditions as Example 1 with the exception that the prereduction step was carried out at 350 C for 2.5 hours in a nitrogen atmosphere containing 5% hydrogen. The results summarized in Table 8 were obtained.
    TABLE 8
    C2H2 conv C2H4 select Green Oil select
    Ex. Catalyst (% by wt) (%) (%) (%)
    29 0.3% Pt, 5.0% In, 99 48 20
    5.0% Ni
  • It will be seen that the Pt—In—Ni catalyst of Example 8 was inferior to the Rh-based catalysts but nevertheless had significantly higher acetylene conversion and produced slightly less green oil than the catalyst of Example 1.
  • While the present invention has been described and illustrated by reference to particular embodiments, those of ordinary skill in the art will appreciate that the invention lends itself to variations not necessarily illustrated herein. For example, it is within the scope of this invention to produce a catalyst composition comprising four or more different metal components. For this reason, reference should be made solely to the appended claims for purposes of determining the true scope of the present invention.

Claims (62)

  1. 1. A catalyst composition comprising at least two metal components selected from Groups 8 to 10 of the Periodic Table of Elements and at least one metal component selected from Group 13 of the Periodic Table of Elements.
  2. 2. The catalyst composition of claim 1 wherein one of said at least two metal components selected from Groups 8 to 10 of the Periodic Table of Elements is rhodium.
  3. 3. The catalyst composition of claim 2 wherein another of said at least two metal components is selected from iron, ruthenium and cobalt.
  4. 4. The catalyst composition of claim 1 wherein said at least one metal component selected from Group 13 of the Periodic Table of Elements is indium.
  5. 5. The catalyst composition of claim 1 and further including a binder and/or support.
  6. 6. A catalyst composition comprising:
    (a) a first component comprising rhodium;
    (b) a second component comprising at least one metal selected from Group 13 of the Periodic Table of Elements; and
    (c) a third component comprising at least one metal different from said first and second components and selected from Groups 1 to 15 of the Periodic Table of Elements.
  7. 7. The catalyst composition of claim 6 and further including a support.
  8. 8. The catalyst composition of claim 7 and comprising from about 0.01 wt % to about 10 wt % of the first component, based on the rhodium metal present by weight of the total weight of the catalyst including the support.
  9. 9. The catalyst composition of claim 7 and comprising from about 0.04 wt % to about 5 wt % of the first component, based on the rhodium metal present by weight of the total weight of the catalyst including the support.
  10. 10. The catalyst composition of claim 7 and comprising from about 0.01 wt % to about 30 wt % of the second component, based on the amount of said Group 13 metal present by weight of the total weight of the catalyst including the support.
  11. 11. The catalyst composition of claim 7 and comprising from about 0.04 wt % to about 20 wt % of the second component, based on the amount of said Group 13 metal present by weight of the total weight of the catalyst including the support.
  12. 12. The catalyst composition of claim 7 wherein said second component comprises indium.
  13. 13. The catalyst composition of claim 12 and comprising from about 0.01 wt % to about 20 wt % of the second component, based on the amount of indium metal present by weight of the total weight of the catalyst including the support.
  14. 14. The catalyst composition of claim 11 and comprising from about 0.04 wt % to about 10 wt % of the second component, based on the amount of indium metal present by weight of the total weight of the catalyst including the support.
  15. 15. The catalyst composition of claim 7 and comprising from about 0.01 wt % to about 50 wt % of the third component, based on the amount of metal of said third component present by weight of the total weight of the catalyst including the support.
  16. 16. The catalyst composition of claim 7 and comprising from about 0.05 wt % to about 30 wt % of the third component, based on the amount of metal of said third component present by weight of the total weight of the catalyst including the support.
  17. 17. The catalyst composition of claim 6 wherein said third component comprises at least one metal selected from Groups 8 to 10 of the Periodic Table of Elements.
  18. 18. The catalyst composition of claim 6 wherein said third component is selected from iron, ruthenium and cobalt.
  19. 19. The catalyst composition of claim 7 wherein the third component is iron and the catalyst composition comprises from about 0.05 wt % to about 30 wt % of the third component, based on the amount of iron metal present by weight of the total weight of the catalyst including the support.
  20. 20. The catalyst composition of claim 7 wherein the third component is iron and the catalyst composition comprises from about 0.1 wt % to about 20 wt % of the third component, based on the amount of iron metal present by weight of the total weight of the catalyst including the support.
  21. 21. The catalyst composition of claim 7 wherein the third component is cobalt and the catalyst composition comprises from about 0.05 wt % to about 30 wt % of the third component, based on the amount of cobalt metal present by weight of the total weight of the catalyst including the support.
  22. 22. The catalyst composition of claim 7 wherein the third component is cobalt and the catalyst composition comprises from about 0.1 wt % to about 25 wt % of the third component, based on the amount of cobalt metal present by weight of the total weight of the catalyst including the support.
  23. 23. The catalyst composition of claim 7 wherein the third component is ruthenium and the catalyst composition comprises from about 0.05 wt % to about 10 wt % of the third component, based on the amount of ruthenium metal present by weight of the total weight of the catalyst including the support.
  24. 24. The catalyst composition of claim 7 wherein the third component is ruthenium and the catalyst composition comprises from about 0.1 wt % to about 5 wt % of the third component, based on the amount of ruthenium metal present by weight of the total weight of the catalyst including the support.
  25. 25. A catalyst composition comprising:
    (a) a first component comprising rhodium;
    (b) a second component comprising indium; and
    (c) a third component selected from one or more of iron, ruthenium and cobalt.
  26. 26. The catalyst composition of claim 25 and further including a support.
  27. 27. The catalyst composition of claim 26 and comprising from about 0.01 wt % to about 10 wt % of the first component, based on the rhodium metal present by weight of the total weight of the catalyst including the support.
  28. 28. The catalyst composition of claim 26 and comprising from about 0.04 wt % to about 5 wt % of the first component, based on the rhodium metal present by weight of the total weight of the catalyst including the support.
  29. 29. The catalyst composition of claim 26 and comprising from about 0.01 wt % to about 20 wt % of the second component, based on the indium metal present by weight of the total weight of the catalyst including the support.
  30. 30. The catalyst composition of claim 26 and comprising from about 0.04 wt % to about 10 wt % of the second component, based on the indium metal present by weight of the total weight of the catalyst including the support.
  31. 31. The catalyst composition of claim 26 wherein the third component is iron and the catalyst composition comprises from about 0.05 wt % to about 30 wt % of the third component, based on the amount of iron metal present by weight of the total weight of the catalyst including the support.
  32. 32. The catalyst composition of claim 26 wherein the third component is iron and the catalyst composition comprises from about 0.1 wt % to about 20 wt % of the third component, based on the amount of iron metal present by weight of the total weight of the catalyst including the support.
  33. 33. The catalyst composition of claim 26 wherein the third component is cobalt and the catalyst composition comprises from about 0.05 wt % to about 30 wt % of the third component, based on the amount of cobalt metal present by weight of the total weight of the catalyst including the support.
  34. 34. The catalyst composition of claim 26 wherein the third component is cobalt and the catalyst composition comprises from about 0.1 wt % to about 25 wt % of the third component, based on the amount of cobalt metal present by weight of the total weight of the catalyst including the support.
  35. 35. The catalyst composition of claim 26 wherein the third component is ruthenium and the catalyst composition comprises from about 0.05 wt % to about 10 wt % of the third component, based on the amount of ruthenium metal present by weight of the total weight of the catalyst including the support.
  36. 36. The catalyst composition of claim 26 wherein the third component is ruthenium and the catalyst composition comprises from about 0.1 wt % to about 5 wt % of the third component, based on the amount of ruthenium metal present by weight of the total weight of the catalyst including the support.
  37. 37. The catalyst composition of claim 25 wherein the molar ratio of rhodium to indium is from about 0.1 to about 1.2.
  38. 38. The catalyst composition of claim 25 wherein the molar ratio of rhodium to indium is from about 0.3 to about 0.9.
  39. 39. The catalyst composition of claim 25 wherein the molar ratio of rhodium to the metal of the third component is from about 0.001 to about 0.6.
  40. 40. The catalyst composition of claim 25 wherein the molar ratio of rhodium to the metal of the third component is from about 0.002 to about 0.3.
  41. 41. The catalyst composition of claim 26 wherein the support is selected from zirconia, alumina and ceria-alumina.
  42. 42. A method of making a catalyst composition, the method comprising:
    (a) applying a rhodium compound to a support;
    (b) applying a compound of a metal selected from Group 13 of the Periodic Table of Elements to the support; and
    (c) applying a compound of a further metal different from rhodium and from said Group 13 metal and selected from Groups 1 to 15 of the Periodic Table of Elements to the support.
  43. 43. The method of claim 42 wherein said further metal compound is applied to the support before either the rhodium compound or the Group 13 metal compound.
  44. 44. The method of claim 42 wherein the rhodium compound and the Group 13 metal compound are applied to the support concurrently.
  45. 45. The method of claim 42 wherein the Group 13 metal compound is applied to the support before the rhodium compound.
  46. 46. The method of claim 42 wherein the rhodium compound is rhodium nitrate.
  47. 47. The method of claim 42 wherein the Group 13 metal compound is an indium compound.
  48. 48. The method of claim 47 wherein the indium compound is indium nitrate or indium formate.
  49. 49. The method of claim 42 wherein the further metal compound is selected from iron, cobalt and ruthenium compounds.
  50. 50. The method of claim 42 wherein at least one of the compounds is applied to the support by impregnating the support with a solution of the compound.
  51. 51. The method of claim 42 wherein at least one of the compounds is applied to the support by precipitating the compound from a solution containing ions of the associated metal.
  52. 52. The method of claim 42 and, after (a) and/or (b) and/or (c), calcining the support at a temperature of about 100° C. to about 600° C.
  53. 53. The method of claim 42 and, after (a), (b) and (c), treating the calcined support in a reducing atmosphere at a temperature in excess of 200° C.
  54. 54. A process for selectively removing alkynes or diolefins from a feedstock also containing olefins, the process comprising contacting the feedstock with hydrogen in the presence of a catalyst composition made by the method of claim 42.
  55. 55. A process for selectively removing alkynes or diolefins from a feedstock also containing olefins, the process comprising contacting the feedstock with hydrogen in the presence of a catalyst composition comprising at least two different metal components selected from Groups 8 to 10 of the Periodic Table of Elements and at least one metal component selected from Group 13 of the Periodic Table of Elements.
  56. 56. The process of claim 55 wherein the alkynes or diolefins have 2 to 4 carbon atoms and the feedstock also contains C2 to C4 olefins.
  57. 57. A process for selectively removing C2 to C4 alkynes or diolefins from a feedstock also containing C2 to C4 olefins, the process comprising contacting the feedstock with hydrogen in the presence of a catalyst composition comprising at least two different metal components selected from Groups 8 to 10 of the Periodic Table of Elements and at least one metal component selected from Group 13 of the Periodic Table of Elements, and the process producing an olefin-enriched product stream containing less than 20 weight % oligomerized alkyne and diolefin compounds, based on the weight of said oligomerized alkyne and diolefin compounds in said product stream by the weight of said feedstock.
  58. 58. The process of claim 57 and producing an olefin-enriched product stream containing less than 10 weight % oligomerized alkyne and diolefin compounds, based on the weight of said oligomerized alkyne and diolefin compounds in said product stream by the weight of said feedstock.
  59. 59. A process for selectively removing alkynes or diolefins from a feedstock also containing olefins, the process comprising contacting the feedstock with hydrogen in the presence of a catalyst composition comprising
    (a) a first component comprising rhodium;
    (b) a second component comprising indium; and
    (c) a third component selected from one or more of iron, ruthenium and cobalt.
  60. 60. The process of claim 59 wherein the alkynes or diolefins have 2 to 4 carbon atoms and the feedstock also contains C2 to C4 olefins.
  61. 61. The process of claim 59 wherein said contacting is conducted at a temperature of from about 20° C. to about 150° C., a pressure of from about 690 kPa to 4100 kPa, and a molar ratio of hydrogen to alkynes and diolefins of from about 1 to about 1000.
  62. 62. The process of claim 59 wherein said contacting is conducted at a temperature of from about 30° C. to about 100° C., a pressure of from about 1400 kPa to 3400 kPa, and a molar ratio of hydrogen to alkynes and diolefins of from about 1.1 to about 800.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7462751B2 (en) 2003-11-24 2008-12-09 Exxonmobil Chemical Patents Inc. Catalyst and process for selective hydrogenation
EP2075061A1 (en) * 2006-09-29 2009-07-01 Cataler Corporation Rhodium carrying chemical and rhodium catalyst prepared using the same
US20120177831A1 (en) * 2008-05-15 2012-07-12 Steven Bruce Dawes Method for making fused ceramic articles of near net shape

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7348463B2 (en) * 2006-03-27 2008-03-25 Catalytic Distillation Technologies Hydrogenation of aromatic compounds
DE102009045804A1 (en) * 2009-10-19 2011-04-21 INSTITUT FüR MIKROTECHNIK MAINZ GMBH Catalyst for the steam reforming of methanol
WO2011143303A3 (en) 2010-05-12 2012-04-12 Shell Internationale Research Maatschappij B.V. Methane aromatization catalyst, method of making and method of using the catalyst

Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3651167A (en) * 1970-08-03 1972-03-21 Universal Oil Prod Co Selective hydrogenation of c4-acetylenic hydrocarbons
US3793232A (en) * 1971-07-05 1974-02-19 Catalyse Soc Prod Francais Reforming catalyst,its manufacture and use
US3859377A (en) * 1973-12-13 1975-01-07 Monsanto Co Selective hydrogenation of c' 4 'acetylenic hydrocarbons
US4149961A (en) * 1976-05-06 1979-04-17 Uop Inc. Hydrocarbon conversion with an acidic multimetallic catalytic composite
US4207169A (en) * 1978-01-06 1980-06-10 Institut Francais Du Petrole Process for the steam dealkylation of aromatic hydrocarbons
US4243516A (en) * 1976-12-06 1981-01-06 Societe Francaise Des Produits Pour Catalyse Catalytic hydroreforming process
US4420420A (en) * 1980-04-14 1983-12-13 Showa Denko Kabushiki Kaisha Rhodium catalyst and method for preparing the same
US4487848A (en) * 1983-06-02 1984-12-11 Uop Inc. Indium-containing catalyst for reforming hydrocarbons
US4522935A (en) * 1983-06-02 1985-06-11 Uop Inc. Platinum and indium-containing catalyst for reforming hydrocarbons
US4677094A (en) * 1986-09-22 1987-06-30 Uop Inc. Trimetallic reforming catalyst
US4691070A (en) * 1984-06-28 1987-09-01 Toa Nenryo Kogyo Kabushiki Kaisha Catalyst, its method of preparation and process for its use in the hydrogenation of diolefins
US5233118A (en) * 1988-12-05 1993-08-03 Uop Steam dehydrogenation process
US5356851A (en) * 1992-04-02 1994-10-18 Institut Francais Du Petrole Catalyst containing a group VIII metal and a group IIIA metal deposited on a support
US5364998A (en) * 1992-04-02 1994-11-15 Institut Francais Du Petrole Process for the selective hydrogenation of hydrocarbons
US5536695A (en) * 1993-12-16 1996-07-16 Institut Francais Du Petrole Dehydrogenation catalysts for C3 C20 parafrins, and preparation thereof
US5877363A (en) * 1996-09-23 1999-03-02 Catalytic Distillation Technologies Process for concurrent selective hydrogenation of acetylenes and 1,2 butadine in hydrocarbon streams
US5965481A (en) * 1993-05-14 1999-10-12 Institut Francais Du Petrole Process for preparing a catalyst suitable for the treatment of exhaust gases from internal combustion engines
US6084140A (en) * 1996-09-11 2000-07-04 Sud-Chemie Nissan Catalyst, Inc. Catalyst for selective hydrogenation of highly unsaturated hydrocarbon compound in olefin compound
US6096933A (en) * 1996-02-01 2000-08-01 Phillips Petroleum Company Hydrocarbon hydrogenation and catalyst therefor
US6153090A (en) * 1997-10-31 2000-11-28 Institut Francais Du Petrole Catalytic hydroreforming process
US6187985B1 (en) * 1997-10-31 2001-02-13 Institut Francais Du Petrole Process for dehydrogenating saturated aliphatic hydrocarbons to olefinic hydrocarbons
US6255548B1 (en) * 1997-10-31 2001-07-03 Institut Francais Du Petrole Process for selective hydrogenation of unsaturated compounds
US6355854B1 (en) * 1999-02-22 2002-03-12 Symyx Technologies, Inc. Processes for oxidative dehydrogenation
US20020068843A1 (en) * 2000-09-29 2002-06-06 Wei Dai Selective hydrogenation catalyst for selectively hydrogenating of unsaturated olefin, process for preparing the same and its use
US6436871B1 (en) * 1999-02-22 2002-08-20 Symyx Technologies, Inc. Catalysts for oxidative dehydrogenation
US6498280B1 (en) * 1999-04-26 2002-12-24 Institut Francais Du Petrole Catalyst comprising an element from groups 8, 9 or 10 with good accessibility, and its use in a paraffin dehydrogenation process
US6503866B1 (en) * 2000-06-05 2003-01-07 Uop Llc Attrition resistant catalyst with reduced surface area
US6514904B1 (en) * 2000-06-05 2003-02-04 Uop Llc Hydrocarbon conversion catalyst and process of using thereof
US6586647B1 (en) * 2001-02-16 2003-07-01 Uop Llc Process for hydrogenating acetylenes

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2286187B1 (en) * 1974-09-25 1978-12-01 Catalyse Soc Prod Francais
US5863856A (en) 1997-04-22 1999-01-26 Exxon Research And Engineering Company Preparation of high activity catalysts the catalysts and their use
US5856261A (en) 1997-04-22 1999-01-05 Exxon Research And Engineering Company Preparation of high activity catalysts; the catalysts and their use
US5856260A (en) 1997-04-22 1999-01-05 Exxon Research And Engineering Company Preparation of high activity catalysts; the catalysts and their use
DE10010007A1 (en) * 1999-03-03 2000-12-21 Toyota Motor Co Ltd Catalyst used for reforming hydrocarbon fuel comprises precious metal and element of groups 2B and 3B on porous metal oxide carrier
GB0227086D0 (en) 2002-11-20 2002-12-24 Exxonmobil Res & Eng Co Hydrogenation processes
US7220701B2 (en) * 2003-11-24 2007-05-22 Exxonmobil Chemical Patents Inc. Catalyst and process for selective hydrogenation
US7199273B2 (en) * 2003-11-24 2007-04-03 Exxonmobil Chemical Patents, Inc. Selective hydrogenation of alkynes and/or diolefins
US7220700B2 (en) * 2003-11-24 2007-05-22 Exxonmobil Chemical Patents Inc. Catalyst and process for selective hydrogenation

Patent Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3651167A (en) * 1970-08-03 1972-03-21 Universal Oil Prod Co Selective hydrogenation of c4-acetylenic hydrocarbons
US3793232A (en) * 1971-07-05 1974-02-19 Catalyse Soc Prod Francais Reforming catalyst,its manufacture and use
US3859377A (en) * 1973-12-13 1975-01-07 Monsanto Co Selective hydrogenation of c' 4 'acetylenic hydrocarbons
US4149961A (en) * 1976-05-06 1979-04-17 Uop Inc. Hydrocarbon conversion with an acidic multimetallic catalytic composite
US4243516A (en) * 1976-12-06 1981-01-06 Societe Francaise Des Produits Pour Catalyse Catalytic hydroreforming process
US4207169A (en) * 1978-01-06 1980-06-10 Institut Francais Du Petrole Process for the steam dealkylation of aromatic hydrocarbons
US4420420A (en) * 1980-04-14 1983-12-13 Showa Denko Kabushiki Kaisha Rhodium catalyst and method for preparing the same
US4522935A (en) * 1983-06-02 1985-06-11 Uop Inc. Platinum and indium-containing catalyst for reforming hydrocarbons
US4487848A (en) * 1983-06-02 1984-12-11 Uop Inc. Indium-containing catalyst for reforming hydrocarbons
US4691070A (en) * 1984-06-28 1987-09-01 Toa Nenryo Kogyo Kabushiki Kaisha Catalyst, its method of preparation and process for its use in the hydrogenation of diolefins
US4677094A (en) * 1986-09-22 1987-06-30 Uop Inc. Trimetallic reforming catalyst
US5233118A (en) * 1988-12-05 1993-08-03 Uop Steam dehydrogenation process
US5356851A (en) * 1992-04-02 1994-10-18 Institut Francais Du Petrole Catalyst containing a group VIII metal and a group IIIA metal deposited on a support
US5364998A (en) * 1992-04-02 1994-11-15 Institut Francais Du Petrole Process for the selective hydrogenation of hydrocarbons
US5965481A (en) * 1993-05-14 1999-10-12 Institut Francais Du Petrole Process for preparing a catalyst suitable for the treatment of exhaust gases from internal combustion engines
US5536695A (en) * 1993-12-16 1996-07-16 Institut Francais Du Petrole Dehydrogenation catalysts for C3 C20 parafrins, and preparation thereof
US6096933A (en) * 1996-02-01 2000-08-01 Phillips Petroleum Company Hydrocarbon hydrogenation and catalyst therefor
US6084140A (en) * 1996-09-11 2000-07-04 Sud-Chemie Nissan Catalyst, Inc. Catalyst for selective hydrogenation of highly unsaturated hydrocarbon compound in olefin compound
US5877363A (en) * 1996-09-23 1999-03-02 Catalytic Distillation Technologies Process for concurrent selective hydrogenation of acetylenes and 1,2 butadine in hydrocarbon streams
US6153090A (en) * 1997-10-31 2000-11-28 Institut Francais Du Petrole Catalytic hydroreforming process
US6187985B1 (en) * 1997-10-31 2001-02-13 Institut Francais Du Petrole Process for dehydrogenating saturated aliphatic hydrocarbons to olefinic hydrocarbons
US6255548B1 (en) * 1997-10-31 2001-07-03 Institut Francais Du Petrole Process for selective hydrogenation of unsaturated compounds
US6436871B1 (en) * 1999-02-22 2002-08-20 Symyx Technologies, Inc. Catalysts for oxidative dehydrogenation
US6355854B1 (en) * 1999-02-22 2002-03-12 Symyx Technologies, Inc. Processes for oxidative dehydrogenation
US6498280B1 (en) * 1999-04-26 2002-12-24 Institut Francais Du Petrole Catalyst comprising an element from groups 8, 9 or 10 with good accessibility, and its use in a paraffin dehydrogenation process
US6503866B1 (en) * 2000-06-05 2003-01-07 Uop Llc Attrition resistant catalyst with reduced surface area
US6514904B1 (en) * 2000-06-05 2003-02-04 Uop Llc Hydrocarbon conversion catalyst and process of using thereof
US20020068843A1 (en) * 2000-09-29 2002-06-06 Wei Dai Selective hydrogenation catalyst for selectively hydrogenating of unsaturated olefin, process for preparing the same and its use
US6586647B1 (en) * 2001-02-16 2003-07-01 Uop Llc Process for hydrogenating acetylenes

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7462751B2 (en) 2003-11-24 2008-12-09 Exxonmobil Chemical Patents Inc. Catalyst and process for selective hydrogenation
EP2075061A1 (en) * 2006-09-29 2009-07-01 Cataler Corporation Rhodium carrying chemical and rhodium catalyst prepared using the same
US20100075841A1 (en) * 2006-09-29 2010-03-25 Akiya Chiba Rhodium-loading solution and rhodium catalyst prepared using the same
EP2075061A4 (en) * 2006-09-29 2011-10-12 Cataler Corp Rhodium carrying chemical and rhodium catalyst prepared using the same
US8691721B2 (en) 2006-09-29 2014-04-08 Cataler Corporation Rhodium-loading solution and rhodium catalyst prepared using the same
US20120177831A1 (en) * 2008-05-15 2012-07-12 Steven Bruce Dawes Method for making fused ceramic articles of near net shape
US8454885B2 (en) * 2008-05-15 2013-06-04 Corning Incorporated Method for making fused ceramic articles of near net shape

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