CA1277652C - Bimetallic catalysts for the reaction of carbon monoxide and hydrogen - Google Patents
Bimetallic catalysts for the reaction of carbon monoxide and hydrogenInfo
- Publication number
- CA1277652C CA1277652C CA000521315A CA521315A CA1277652C CA 1277652 C CA1277652 C CA 1277652C CA 000521315 A CA000521315 A CA 000521315A CA 521315 A CA521315 A CA 521315A CA 1277652 C CA1277652 C CA 1277652C
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- Prior art keywords
- alumina
- support
- catalyst
- carbonyl
- oxide
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/15—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively
- C07C29/151—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases
- C07C29/153—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used
- C07C29/156—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals or compounds thereof
- C07C29/157—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals or compounds thereof containing platinum group metals or compounds thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts 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
- B01J23/56—Platinum group metals
- B01J23/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/652—Chromium, molybdenum or tungsten
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C27/00—Processes involving the simultaneous production of more than one class of oxygen-containing compounds
- C07C27/04—Processes involving the simultaneous production of more than one class of oxygen-containing compounds by reduction of oxygen-containing compounds
- C07C27/06—Processes involving the simultaneous production of more than one class of oxygen-containing compounds by reduction of oxygen-containing compounds by hydrogenation of oxides of carbon
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/15—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively
- C07C29/151—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases
- C07C29/153—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used
- C07C29/156—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals or compounds thereof
- C07C29/157—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals or compounds thereof containing platinum group metals or compounds thereof
- C07C29/158—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals or compounds thereof containing platinum group metals or compounds thereof containing rhodium or compounds thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Abstract
NOVEL BIMETALLIC CATALYSTS FOR THE REACTION OF
CARBON MONOXIDE AND HYDROGEN
ABSTRACT OF THE DISCLOSURE
For the reaction of CO and H2 to produce hydro-carbons and alcohols, catalysts prepared by depositing carbonyls of molybdenum or tungsten and rhodium or ruthenium on alumina support and decomposing and oxidizing the carbonyls to oxides of the metals on the support.
CARBON MONOXIDE AND HYDROGEN
ABSTRACT OF THE DISCLOSURE
For the reaction of CO and H2 to produce hydro-carbons and alcohols, catalysts prepared by depositing carbonyls of molybdenum or tungsten and rhodium or ruthenium on alumina support and decomposing and oxidizing the carbonyls to oxides of the metals on the support.
Description
"517 ~ ~ ~7 ~S~
NOVEL BIM~TALLIC CATALYSTS FOR THE REACTION OF
_CARBON MONOXIDE AND HYDROGEN
The invention relates to improvements in cata-lysts for the catalytic reaction of carbon monoxide and hydrogen to produce hydrocarbons and oxygenated compounds, and to the use of such catalysts in such reactions. The invention provides improved catalysts and an improved method of making such catalysts and an improved process using such catalysts.
There is much prior ar~ relating to catalysts for use in the Fischer-Tropsch synthesis. More partic-ularly, catalysts having a combination of a Group VI Bmetal, e.g. Mo or W with a Group VIII metal 9 e.g. Rh or Ru, on alumina supports have been described for use in such reactions.
U.S. Patent No. ~,210,597 described use of rhodium tungsten catalysts with some sodium in the cata-lyst to promote oxygenation and decrease methanation, with the result that yields of the lower aliphatic acid and alcohol products were improved. Using the same catalyst but without sodium caused the production of hydrocarbons to predominate with only minimal oxygenated products. The patent stated and demonstrated that without sodium, the rhodium-tungsten catalyst described would be fairly active for producing hydrocarbons but would have little or no activity for producing the more valuable oxygenated com-pounds.
Use of manganese or iron with Rh-Mo or Rh-W as catalyst for the reaction of H2 with CO to favor the pro-duction of two-carbon oxygenation products, was described in U.S. Patent No. 4,096,164.
~2~7~S2 One object of the invention is to provide a method of making catalysts for the catalytic reaction of CO and H2, and the catalysts so made, which can produce conversion selectively to methanol and ethanol as oxy-genate products. Most of the remaining conversion prod-ucts are the hydrocarbon products of methanation.
Another object is to provide a method of making catalysts comprising molybdenum or tungsten and rhodium or ruthenium on an alumina support, and the catalysts so made, which can produce significant oxygenate yields without the need for addition of other elements such as sodium or manganese or iron.
Catalysts of the invention are prepared by im-; pregnating an alumina catalyst support with compounds of Mo or W and Rh or Ru. The alumina support is preferably aprecipitated alumina, for example Cyanamid's Aero, ~-Al2O3 having nominal surface area of 270 m2/gm and pore volume of 0.6 cc/gm. Other useful supports of ~-A12O3 include Alumoxide-C, (Degussa) and Catapal-B-(Conoco) prepared by hydrolysis of the alkoxides or halides of alumina. Useful alumina supports may include other in-gredients in minor proportions, in addition to alumina as the principal ingredient, such as silica, magnesia, zir-conia, titania, etc. in amounts up to about 5 percent by weight. Other alumina supports having surface areas of about 200-300 m2/gm, pore volumes of about 0.4 to 0.8 cc/gm and impurity levels of less than 0.1 to 1 percent by weight are also suitable for use in the invention. The catalyst support may be in the form of alumina powder or shaped alumina particles.
The preparation of the catalysts, and partic-ularly the method of depositing the metals on the support, are important to the catalytic activity and selectivity of conversion that are obtained when the catalyst is used in the catalytic process. A carbonyl compound of the sel-ected molybdenum or tungsten metal is dissolved in an organic solvent, and the alumina support is impregnated by * Trade Mark ~;~776~2 slurrying particulate alumina in the solution and refluxing the slurry for a time sufficient to chemisorb the metal carbonyl on the alumina. The carbonyl is then decomposed and oxidized on the alumina, leaving the metal oxide dispersed on the surface area of the alumina~
r~he carbonyl of the selected rhodium or ruthenium metal is similarly deposited, decomposed and oxidized on the same support, leaving Rh or Ru oxide dispersed on the alumina support which had been previously impregnated with the oxide of Mo or W. Subsequent oxidation and decomposition of the carbonyl on the support leads to deposition of the metal oxide of Rh or Ru over the oxide of Mo or W on the support. The Rh or Ru oxide is thus deposited using the same procedure that was previously used to deposit the Mo or W oxide.
The catalysts can also be prepared as fo~lowsO A carbonyl compound of the selected molybdenum or tungsten metal is dissolved in an organic solvent. The alumina support is impre~nated by slurrying particulate alumina in the solution and refluxing the slurry for time sufficient to chemisorb the metal carbonyl on the surface area of the alumina. The carbonyl of the selected rhodium or ruthenium metal is then similarly deposited on the same parti-cles onto which the metal carbonyl of Mo or W was previously chemisorbed. Those particles are slurried in a carbonyl solution of Rh or Ru and the slurry is refluxed for time sufficient to chemisorb the metal carbonyl of Rh or Ru. Subsequent decomposition and oxidation of the carbonyls of the two metals on the support ~ 3a ~%7~652 leads to formation of Rh or Ru oxide over the oxide of Mo or W
on the support.
It is important to deposit the W or Mo before the Rh or Ru is deposited. The use of metal carbonyl solutions for deposition of the metals is also important. By these procedures we obtain a unique surface epitaxy of the second metal oxide deposited over the first on the ~: `
Z7~765iZ
support.
The molybdenum or tungsten oxide is bound strongly to the surface of the alumina support through shared oxygen atoms as an epitaxial layer. The rhodium or ruthenium oxide i5 bound in turn to the molybdenum or tungsten oxide on the support. The molybdenum or tungsten oxide anchors the rhodium or ruthenium oxide to the support. The cakalytic metals are thus evenly dispersed over the surface area of the support in a unique surface epitaxial structure. We believe this unique surface epitaxy of the catalytic metals results from the method of making the catalyst and accounts for the good yields and good selectivity of conversion to methanol and e-thanol products which can be obtained even under mild conditions using these catalysts in the process of the invention~
Accordingly, the invention herein comprises catalyst for the reaction of synthesis gas containing hydrogen and carbon monoxide for selective production of oxygenates comprising a support of alumina which may contain up to about 5% of other oxidesr molybdenum or tungsten in the range of 1 to lO percent by weight deposited as the metal oxide on the surface area of the alumina support by chemisorption from solution and oxidation of molybdenum or tungsten carbonyl on the surface of said alumina and ~urther comprising rhodium or ruthenium in the range 0.5 to 5 percent by weight deposited as the metal oxide by chemisorption from solution and oxidation of the chemisorbed carbonyl of rhodium or ruthenium over said molybdenum or tungsten oxide on the support.
C' ~ ~ /
~77G~
~a 61109-7490 The invention further comprises a method of making a catalyst having molybdenum or tungsten oxide and rhodium or ruthenium oxide on a catalyst support of alumina, said method comprising adsorbing the carbonyl of molybdenum or tungsten on the surface area of the alumina support and decomposing and oxidizing the adsorbed metal carbonyl to metal oxide, adsorbing the carbonyl of rhodium or ruthenium over the molybdenum or tungsten carbonyl or oxide on the support and decomposing and oxidi~ing the adsorbed metal carbonyl to metal oxides on the support.
The invention is described in more detail in detailed examples below, which demonstrate advantages of the invention. ~y using higher operating pressures for the catalytic reaction than those used in the examples, one may produce even higher conversions with as good or better yields of the oxygenate products.
A solution of 3.684 g W(CO)6 in 150 ml heptane is prepared. Alumina is prepared by heating precipitated alumina powder in a stream of air at 300C for 90 minutes. A slurry is made with 30 grams of the prepared alumina in the tungsten carbonyl solution. The slurry is refluxed for two hours in a flow oE nitrogen, then cooled and vacuum filtered. The filtered solids are dried in air at 120C. The tungsten carbonyl has decomposed leaving an oxide of tungsten dispersed on the alumina support.
277~2 4b 61109-7490 Then a five gram aliquot of this material is slurried in a solution of 0.326 g. Ru3(C0)12 in lO0 ml heptane. The slurry is refluxed under nitrogen for two hours then cooled, vacuum filtered and dried in air at 120C. The ruthenium carbonyl has been deposited and converted to oxide of ruthenium over an oxide of tungsten, on the ,. . .
, ,, j ~ ~7 ~2 support. The finished catalyst is nominally 3% Ru-6%
WlAl2o3 A solution of 5.319 g. Mo~C0)6 in 150 ml heptane is prepared. Alumina powder is prepared by heating in a stream of air at 300C for 90 minutes. A slurry is made with 30 grams of the prepared alumina in the malybde~um carbonyl solution. The slurry is refluxed for two hours in a flow of nitrogen, then cooled and vacuum filtered.
The filtered solids are dried in air at 120C. The mo-lybdenum carbonyl has decomposed leaving an oxide of molybdenum dispersed on the alumina support. Then a ten gram aliquot of this material is slurried in a solution of 0.652 gms of Ru3(C0)12 in 100 ml heptane. The slurry is refluxed under nitrogen for two hours then cooled, vacuum filtered and dried in air at 120C. The ruthenium has been deposited as ruthenium oxide over the molybdenum oxide on the support. The finished catalyst is nominally 3% Ru - 6% Mo/A1203.
A solution of 0.355 g. Mo(C0)6 in 100 ml heptane is prepared. Alumina is prepared by heating in a stream of air at 300C for 90 minutes. A slurry is made with 2 g. of the prepared alumina in the molybdenum carbonyl solution. The slurry is refluxed for two and one half hours in a flow of nitrogen~ and cooled to room temper-ature. Under a purge of nitrogen 0.156 g. of Rh(C0)2 (acetylacetonate) is added to the slurry. The resultant slurry is refluxed in a flow of nitrogen for an additional ~our then cooled, vacuum filtered and dried in air at 120C. The rhodium has been deposited as the carbonyl over the molybdenum carbonyl and both are decomposed in air leaving oxide of rhodium over an oxide of molybdenum, on the support. The finished catalyst is nominally 3% Rh -6% Mo/A1203 A solution of 0.246 g. W(C0)6 in 100 ml heptane is prepared. Alumina is prepared by heating in a stream of air at 300C for 90 minutes. A slurry is made with 2 g of the prepared alumina in the tungsten carbonyl solution.
The slurry is refluxed for two and one half hours in a flow of nitrogen, and cooled to room temperature.
Under a purge of nitrogen 0.156 g. of Rh(CO~2 (acetylacetonate) is added to the slurry. The resultant slurry is refluxed in a flow of nitrogen for an additional hour then cooled, vacuum filtered and dried in air at 120C. The rhodium has been deposited as an oxide of rhodium over an oxide of tungsten, on the support. The finished catalyst is nominally 3% Rh - 6% W/A1203.
A Ru/A12O3 control sample is prepared by slurry-ing 3.22 g. A1203 in a solution of 0.21 g. Ru3(CO)12 in 100 ml heptane and refluxing the slurry under N2 for two hours. The slurry is then filtered and dried in air yielding a catalyst of nominally 3% ~u/A12O3.
Catalysts prepared in Examples 1 to 5 are used as catalysts for the reaction of ~he syngas mixture of H2 and CO by the following procedure. 0.5 Cm3 of 40 x 80 mesh of the catalyst sample are packed into a fixed-bed micro-reactor capable of operating at 1 to 5 atmospheres total pressure. The catalysts are reduced in situ in flowing hydrogen at 450C at atmospheric pressure. The syngas is supplied at a fixed 1:1 ratio in a cylinder of the pre-mixed gases. Gas flow rates are controlled with a cali-brated mass flow meter. Gas flows vary from 2 to 20 cm3/min corresponding to 240 to 2400 hr~l respectively.
The hydrocarbons, oxygenates, water, carbon dioxide and unreacted feed exit the reactor and are analyzed on-line with two gas chromatographs, suitable for the analysis of hydrocarbons and oxygenates, as well as the C02, H2 and C0 respectively. The results of these experiments with each of the catalysts in Examples 1 to 5 are presented in Tables I and II.
l~6~æ
The catalysts of this invention are shown to have both high activity for the conversion of CO and hydrogen to hydrocarbons and an ability to also produce a signif-icant yield of oxygenated products, especially methanol and ethanol, under very mild process conditions.
In addition to the production of significant yields of hydrocarbons and oxygenate when using catalysts according to the invention, as shown in Table II, hydro-carbons which are produced by the syngas reaction with these catalysts are found to contain generally higher proportions of aliphatic hydrocarbons having 2 ~o 6 carbon atoms, and those aliphatics are found to contain generally higher proportions of olefin to parafin hydrocarbvns, as compared in Table I with reaction products from processes that use catalysts of only ruthenium or only rhodium on : alumina, without molybdenum.
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NOVEL BIM~TALLIC CATALYSTS FOR THE REACTION OF
_CARBON MONOXIDE AND HYDROGEN
The invention relates to improvements in cata-lysts for the catalytic reaction of carbon monoxide and hydrogen to produce hydrocarbons and oxygenated compounds, and to the use of such catalysts in such reactions. The invention provides improved catalysts and an improved method of making such catalysts and an improved process using such catalysts.
There is much prior ar~ relating to catalysts for use in the Fischer-Tropsch synthesis. More partic-ularly, catalysts having a combination of a Group VI Bmetal, e.g. Mo or W with a Group VIII metal 9 e.g. Rh or Ru, on alumina supports have been described for use in such reactions.
U.S. Patent No. ~,210,597 described use of rhodium tungsten catalysts with some sodium in the cata-lyst to promote oxygenation and decrease methanation, with the result that yields of the lower aliphatic acid and alcohol products were improved. Using the same catalyst but without sodium caused the production of hydrocarbons to predominate with only minimal oxygenated products. The patent stated and demonstrated that without sodium, the rhodium-tungsten catalyst described would be fairly active for producing hydrocarbons but would have little or no activity for producing the more valuable oxygenated com-pounds.
Use of manganese or iron with Rh-Mo or Rh-W as catalyst for the reaction of H2 with CO to favor the pro-duction of two-carbon oxygenation products, was described in U.S. Patent No. 4,096,164.
~2~7~S2 One object of the invention is to provide a method of making catalysts for the catalytic reaction of CO and H2, and the catalysts so made, which can produce conversion selectively to methanol and ethanol as oxy-genate products. Most of the remaining conversion prod-ucts are the hydrocarbon products of methanation.
Another object is to provide a method of making catalysts comprising molybdenum or tungsten and rhodium or ruthenium on an alumina support, and the catalysts so made, which can produce significant oxygenate yields without the need for addition of other elements such as sodium or manganese or iron.
Catalysts of the invention are prepared by im-; pregnating an alumina catalyst support with compounds of Mo or W and Rh or Ru. The alumina support is preferably aprecipitated alumina, for example Cyanamid's Aero, ~-Al2O3 having nominal surface area of 270 m2/gm and pore volume of 0.6 cc/gm. Other useful supports of ~-A12O3 include Alumoxide-C, (Degussa) and Catapal-B-(Conoco) prepared by hydrolysis of the alkoxides or halides of alumina. Useful alumina supports may include other in-gredients in minor proportions, in addition to alumina as the principal ingredient, such as silica, magnesia, zir-conia, titania, etc. in amounts up to about 5 percent by weight. Other alumina supports having surface areas of about 200-300 m2/gm, pore volumes of about 0.4 to 0.8 cc/gm and impurity levels of less than 0.1 to 1 percent by weight are also suitable for use in the invention. The catalyst support may be in the form of alumina powder or shaped alumina particles.
The preparation of the catalysts, and partic-ularly the method of depositing the metals on the support, are important to the catalytic activity and selectivity of conversion that are obtained when the catalyst is used in the catalytic process. A carbonyl compound of the sel-ected molybdenum or tungsten metal is dissolved in an organic solvent, and the alumina support is impregnated by * Trade Mark ~;~776~2 slurrying particulate alumina in the solution and refluxing the slurry for a time sufficient to chemisorb the metal carbonyl on the alumina. The carbonyl is then decomposed and oxidized on the alumina, leaving the metal oxide dispersed on the surface area of the alumina~
r~he carbonyl of the selected rhodium or ruthenium metal is similarly deposited, decomposed and oxidized on the same support, leaving Rh or Ru oxide dispersed on the alumina support which had been previously impregnated with the oxide of Mo or W. Subsequent oxidation and decomposition of the carbonyl on the support leads to deposition of the metal oxide of Rh or Ru over the oxide of Mo or W on the support. The Rh or Ru oxide is thus deposited using the same procedure that was previously used to deposit the Mo or W oxide.
The catalysts can also be prepared as fo~lowsO A carbonyl compound of the selected molybdenum or tungsten metal is dissolved in an organic solvent. The alumina support is impre~nated by slurrying particulate alumina in the solution and refluxing the slurry for time sufficient to chemisorb the metal carbonyl on the surface area of the alumina. The carbonyl of the selected rhodium or ruthenium metal is then similarly deposited on the same parti-cles onto which the metal carbonyl of Mo or W was previously chemisorbed. Those particles are slurried in a carbonyl solution of Rh or Ru and the slurry is refluxed for time sufficient to chemisorb the metal carbonyl of Rh or Ru. Subsequent decomposition and oxidation of the carbonyls of the two metals on the support ~ 3a ~%7~652 leads to formation of Rh or Ru oxide over the oxide of Mo or W
on the support.
It is important to deposit the W or Mo before the Rh or Ru is deposited. The use of metal carbonyl solutions for deposition of the metals is also important. By these procedures we obtain a unique surface epitaxy of the second metal oxide deposited over the first on the ~: `
Z7~765iZ
support.
The molybdenum or tungsten oxide is bound strongly to the surface of the alumina support through shared oxygen atoms as an epitaxial layer. The rhodium or ruthenium oxide i5 bound in turn to the molybdenum or tungsten oxide on the support. The molybdenum or tungsten oxide anchors the rhodium or ruthenium oxide to the support. The cakalytic metals are thus evenly dispersed over the surface area of the support in a unique surface epitaxial structure. We believe this unique surface epitaxy of the catalytic metals results from the method of making the catalyst and accounts for the good yields and good selectivity of conversion to methanol and e-thanol products which can be obtained even under mild conditions using these catalysts in the process of the invention~
Accordingly, the invention herein comprises catalyst for the reaction of synthesis gas containing hydrogen and carbon monoxide for selective production of oxygenates comprising a support of alumina which may contain up to about 5% of other oxidesr molybdenum or tungsten in the range of 1 to lO percent by weight deposited as the metal oxide on the surface area of the alumina support by chemisorption from solution and oxidation of molybdenum or tungsten carbonyl on the surface of said alumina and ~urther comprising rhodium or ruthenium in the range 0.5 to 5 percent by weight deposited as the metal oxide by chemisorption from solution and oxidation of the chemisorbed carbonyl of rhodium or ruthenium over said molybdenum or tungsten oxide on the support.
C' ~ ~ /
~77G~
~a 61109-7490 The invention further comprises a method of making a catalyst having molybdenum or tungsten oxide and rhodium or ruthenium oxide on a catalyst support of alumina, said method comprising adsorbing the carbonyl of molybdenum or tungsten on the surface area of the alumina support and decomposing and oxidizing the adsorbed metal carbonyl to metal oxide, adsorbing the carbonyl of rhodium or ruthenium over the molybdenum or tungsten carbonyl or oxide on the support and decomposing and oxidi~ing the adsorbed metal carbonyl to metal oxides on the support.
The invention is described in more detail in detailed examples below, which demonstrate advantages of the invention. ~y using higher operating pressures for the catalytic reaction than those used in the examples, one may produce even higher conversions with as good or better yields of the oxygenate products.
A solution of 3.684 g W(CO)6 in 150 ml heptane is prepared. Alumina is prepared by heating precipitated alumina powder in a stream of air at 300C for 90 minutes. A slurry is made with 30 grams of the prepared alumina in the tungsten carbonyl solution. The slurry is refluxed for two hours in a flow oE nitrogen, then cooled and vacuum filtered. The filtered solids are dried in air at 120C. The tungsten carbonyl has decomposed leaving an oxide of tungsten dispersed on the alumina support.
277~2 4b 61109-7490 Then a five gram aliquot of this material is slurried in a solution of 0.326 g. Ru3(C0)12 in lO0 ml heptane. The slurry is refluxed under nitrogen for two hours then cooled, vacuum filtered and dried in air at 120C. The ruthenium carbonyl has been deposited and converted to oxide of ruthenium over an oxide of tungsten, on the ,. . .
, ,, j ~ ~7 ~2 support. The finished catalyst is nominally 3% Ru-6%
WlAl2o3 A solution of 5.319 g. Mo~C0)6 in 150 ml heptane is prepared. Alumina powder is prepared by heating in a stream of air at 300C for 90 minutes. A slurry is made with 30 grams of the prepared alumina in the malybde~um carbonyl solution. The slurry is refluxed for two hours in a flow of nitrogen, then cooled and vacuum filtered.
The filtered solids are dried in air at 120C. The mo-lybdenum carbonyl has decomposed leaving an oxide of molybdenum dispersed on the alumina support. Then a ten gram aliquot of this material is slurried in a solution of 0.652 gms of Ru3(C0)12 in 100 ml heptane. The slurry is refluxed under nitrogen for two hours then cooled, vacuum filtered and dried in air at 120C. The ruthenium has been deposited as ruthenium oxide over the molybdenum oxide on the support. The finished catalyst is nominally 3% Ru - 6% Mo/A1203.
A solution of 0.355 g. Mo(C0)6 in 100 ml heptane is prepared. Alumina is prepared by heating in a stream of air at 300C for 90 minutes. A slurry is made with 2 g. of the prepared alumina in the molybdenum carbonyl solution. The slurry is refluxed for two and one half hours in a flow of nitrogen~ and cooled to room temper-ature. Under a purge of nitrogen 0.156 g. of Rh(C0)2 (acetylacetonate) is added to the slurry. The resultant slurry is refluxed in a flow of nitrogen for an additional ~our then cooled, vacuum filtered and dried in air at 120C. The rhodium has been deposited as the carbonyl over the molybdenum carbonyl and both are decomposed in air leaving oxide of rhodium over an oxide of molybdenum, on the support. The finished catalyst is nominally 3% Rh -6% Mo/A1203 A solution of 0.246 g. W(C0)6 in 100 ml heptane is prepared. Alumina is prepared by heating in a stream of air at 300C for 90 minutes. A slurry is made with 2 g of the prepared alumina in the tungsten carbonyl solution.
The slurry is refluxed for two and one half hours in a flow of nitrogen, and cooled to room temperature.
Under a purge of nitrogen 0.156 g. of Rh(CO~2 (acetylacetonate) is added to the slurry. The resultant slurry is refluxed in a flow of nitrogen for an additional hour then cooled, vacuum filtered and dried in air at 120C. The rhodium has been deposited as an oxide of rhodium over an oxide of tungsten, on the support. The finished catalyst is nominally 3% Rh - 6% W/A1203.
A Ru/A12O3 control sample is prepared by slurry-ing 3.22 g. A1203 in a solution of 0.21 g. Ru3(CO)12 in 100 ml heptane and refluxing the slurry under N2 for two hours. The slurry is then filtered and dried in air yielding a catalyst of nominally 3% ~u/A12O3.
Catalysts prepared in Examples 1 to 5 are used as catalysts for the reaction of ~he syngas mixture of H2 and CO by the following procedure. 0.5 Cm3 of 40 x 80 mesh of the catalyst sample are packed into a fixed-bed micro-reactor capable of operating at 1 to 5 atmospheres total pressure. The catalysts are reduced in situ in flowing hydrogen at 450C at atmospheric pressure. The syngas is supplied at a fixed 1:1 ratio in a cylinder of the pre-mixed gases. Gas flow rates are controlled with a cali-brated mass flow meter. Gas flows vary from 2 to 20 cm3/min corresponding to 240 to 2400 hr~l respectively.
The hydrocarbons, oxygenates, water, carbon dioxide and unreacted feed exit the reactor and are analyzed on-line with two gas chromatographs, suitable for the analysis of hydrocarbons and oxygenates, as well as the C02, H2 and C0 respectively. The results of these experiments with each of the catalysts in Examples 1 to 5 are presented in Tables I and II.
l~6~æ
The catalysts of this invention are shown to have both high activity for the conversion of CO and hydrogen to hydrocarbons and an ability to also produce a signif-icant yield of oxygenated products, especially methanol and ethanol, under very mild process conditions.
In addition to the production of significant yields of hydrocarbons and oxygenate when using catalysts according to the invention, as shown in Table II, hydro-carbons which are produced by the syngas reaction with these catalysts are found to contain generally higher proportions of aliphatic hydrocarbons having 2 ~o 6 carbon atoms, and those aliphatics are found to contain generally higher proportions of olefin to parafin hydrocarbvns, as compared in Table I with reaction products from processes that use catalysts of only ruthenium or only rhodium on : alumina, without molybdenum.
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Claims (16)
1. Catalyst for the reaction of synthesis gas containing hydrogen and carbon monoxide for selective production of oxygenates comprising a support of alumina which may contain up to about 5%
of other oxides, molybdenum or tungsten in the range of 1 to 10 percent by weight deposited as the metal oxide on the surface area of the alumina support by chemisorption from solution and oxidation of molybdenum or tungsten carbonyl on the surface of said alumina and further comprising rhodium or ruthenium in the range 0.5 to 5 percent by weight deposited as the metal oxide by chemisorption from solution and oxidation of the chemisorbed carbonyl of rhodium or ruthenium over said molybdenum or tungsten oxide on the support.
of other oxides, molybdenum or tungsten in the range of 1 to 10 percent by weight deposited as the metal oxide on the surface area of the alumina support by chemisorption from solution and oxidation of molybdenum or tungsten carbonyl on the surface of said alumina and further comprising rhodium or ruthenium in the range 0.5 to 5 percent by weight deposited as the metal oxide by chemisorption from solution and oxidation of the chemisorbed carbonyl of rhodium or ruthenium over said molybdenum or tungsten oxide on the support.
2. A method of making a catalyst having molybdenum or tung-sten oxide and rhodium or ruthenium oxide on a catalyst support of alumina, said method comprising adsorbing the carbonyl of molybdenum or tungsten on the surface area of the alumina support and decompos-ing and oxidizing the adsorbed metal carbonyl to metal oxide, adsorbing the carbonyl of rhodium or ruthenium over the molybdenum or tungsten carbonyl or oxide on the support and decomposing and oxidizing the adsorbed metal carbonyl to metal oxides on the support.
3. A catalyst according to claim 1 wherein the alumina con-tains up to about 5% by weight of other ingredients.
4. A catalyst according to claim 1 wherein the alumina con-tains up to about 5% by weight of other ingredients chosen from silica, magnesia, zirconia and titania.
5. A catalyst according to claim 1 wherein the alumina has a surface area of from about 200 to about 300 m2/gm.
6. A catalyst according to claim 1 wherein the alumina has a pore volume of from about 0.4 to about 0.8 cc/gm.
7. A catalyst according to claim 1 wherein the alumina has an impurity level of from about 0.1 to about 1.0 percent by weight.
8. A catalyst according to claim 1 wherein the alumina catalyst support is in the form of a powder.
9. A catalyst according to claim 1 wherein the alumina catalyst support is in the form of shaped alumina particles.
10. A method according to claim 2 wherein the alumina contains up to about 5% by weight of other ingredients.
11. A method according to claim 2 wherein the alumina contains up to about 5% by weight of other ingredients chosen from silica, magnesia, zirconia and titania.
12. A method according to claim 2 wherein the alumina has a surface area of from about 200 to about 300 m2/gm.
13. A method according to claim 2 wherein the alumina has a pore volume of from about 0.4 to about 0.8 cc/gm.
14. A method according to claim 2 wherein the alumina has an impurity level of from about 0.1 to about 1.0 percent by weight.
15. A method according to claim 2 wherein the alumina catalyst support is in the form of a powder.
16. A method according to claims 2 wherein the alumina catalyst support is in the form of shaped alumina particles.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/791,648 US4684618A (en) | 1985-10-28 | 1985-10-28 | Bimetallic catalysts for the reaction of carbon monoxide and hydrogen and method of making the catalysts |
| US791,648 | 1985-10-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1277652C true CA1277652C (en) | 1990-12-11 |
Family
ID=25154351
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000521315A Expired - Fee Related CA1277652C (en) | 1985-10-28 | 1986-10-24 | Bimetallic catalysts for the reaction of carbon monoxide and hydrogen |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4684618A (en) |
| EP (1) | EP0220477A3 (en) |
| JP (1) | JPS62102831A (en) |
| CA (1) | CA1277652C (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2767721B1 (en) * | 1997-08-29 | 1999-10-22 | Inst Francais Du Petrole | NOVEL CATALYSTS FOR USE IN ORGANIC COMPOUND TRANSFORMATION REACTIONS |
| AUPQ439299A0 (en) * | 1999-12-01 | 1999-12-23 | Silverbrook Research Pty Ltd | Interface system |
| JP3715482B2 (en) * | 1999-11-04 | 2005-11-09 | エヌ・イーケムキャット株式会社 | Carbon monoxide selective oxidation catalyst in hydrogen-containing gas, carbon monoxide removal method using the catalyst, and solid polymer electrolyte fuel cell system |
| DE10208254A1 (en) * | 2002-02-26 | 2003-09-04 | Bayer Ag | catalyst |
| US8394861B2 (en) * | 2007-06-27 | 2013-03-12 | Hrd Corporation | Gasification of carbonaceous materials and gas to liquid processes |
| JP5336714B2 (en) * | 2007-08-20 | 2013-11-06 | 株式会社日本触媒 | Ring opening method of cyclic ether |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4096164A (en) * | 1976-08-30 | 1978-06-20 | Union Carbide Corporation | Process for producing ethanol, acetic acid and/or acetaldehyde, from synthesis gas |
| US4328129A (en) * | 1979-12-14 | 1982-05-04 | Ethyl Corporation | Catalyst for making dimethyl ether and methanol from synthesis gas |
| DE3203060A1 (en) * | 1982-01-30 | 1983-08-04 | Hoechst Ag, 6230 Frankfurt | METHOD FOR PRODUCING ACETIC ACID, ACETALDEHYDE AND ETHANOL |
| US4434248A (en) * | 1982-09-29 | 1984-02-28 | Texaco Inc. | Process for preparing alkanols from synthesis gas |
| GB8334155D0 (en) * | 1983-12-22 | 1984-02-01 | Ici Plc | Catalytic composition |
-
1985
- 1985-10-28 US US06/791,648 patent/US4684618A/en not_active Expired - Lifetime
-
1986
- 1986-09-18 EP EP86112925A patent/EP0220477A3/en not_active Ceased
- 1986-10-02 JP JP61233381A patent/JPS62102831A/en active Pending
- 1986-10-24 CA CA000521315A patent/CA1277652C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP0220477A3 (en) | 1988-06-15 |
| EP0220477A2 (en) | 1987-05-06 |
| JPS62102831A (en) | 1987-05-13 |
| US4684618A (en) | 1987-08-04 |
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