| PATENT ASSIGNEE'S COUNTRY | USA |
| UPDATE | 08.00 |
| PATENT NUMBER | This data is not available for free |
| PATENT GRANT DATE | 01.08.00 |
| PATENT TITLE |
Hydrocarbon hydrogenation and catalyst therefor |
| PATENT ABSTRACT | A supported hydrogenation catalyst composition is disclosed which comprises a palladium component, at least one alkali metal iodide such as, for example, potassium iodide, and an inorganic support material such as alumina. The palladium component is concentrated in an area within about 150 microns of the exterior surface of the composition. Also disclosed is a selective hydrogenation process in which diolefins and/or alkynes are hydrogenated with hydrogen to corresponding monoolefins. |
| PATENT INVENTORS | This data is not available for free |
| PATENT ASSIGNEE | This data is not available for free |
| PATENT FILE DATE | 13.03.98 |
| PATENT REFERENCES CITED | This data is not available for free |
| PATENT PARENT CASE TEXT | This data is not available for free |
| PATENT CLAIMS |
1. A composition useful in selectively hydrogenating diolefins and alkynes to monoolefins consisting essentially of: (a) at least one palladium-containing material selected from the group consisting of palladium metal and palladium oxides, (b) at least one alkali metal iodide, and (c) at least one inorganic support material, wherein said composition comprises about 0.01 weight-% palladium to about 2 weight-% palladium (on a total catalyst composition weight basis) and about 0.02 weight-% alkali metal to about 10 weight-% alkali metal (on a total catalyst composition weight basis) with said palladium concentrated in the skin of said composition. |
| PATENT DESCRIPTION |
FIELD OF THE INVENTION This invention relates to a supported noble metal catalyst composition and to a process for selectively hydrogenating diolefins (alkadienes) and alkynes to monoolefins (alkenes) employing a supported noble metal catalyst composition. BACKGROUND OF THE INVENTION Catalysts comprising palladium and a support material are known catalysts for dienes and/or alkynes hydrogenation. Even though these catalysts are effective hydrogenation catalysts, some such catalysts tend to produce green oil by oligomerizing the alkynes and dienes. The green oil has 6 or more carbons per molecule and is not desirable in the production of an alkene such as, for example, ethylene because it fouls the catalyst and cuts the yield to alkene. Therefore, there is an ever present need for further improvements of a selective hydrogenation process to achieve enhanced selectivity to monoolefins, or increased catalyst life, or both. Accordingly, development of a modified supported palladium catalyst composition and its use in processes for the selective hydrogenation of diolefins (alkadienes) or alkynes to monoolefins (alkenes) would be a significant contribution to the art. SUMMARY OF THE INVENTION It is an object of this invention to provide an improved palladium-containing composition which can be useful as a catalyst in the selective hydrogenation of diolefins and/or alkynes to monoolefins. It is another object of this invention to employ this improved catalyst composition in the selective hydrogenation of diolefins or alkynes to monoolefins. It is also an object of this invention to employ this improved catalyst composition in the selective hydrogenation of alkadienes and alkynes to the corresponding alkenes. It is another object of this invention to employ this improved catalyst composition in the selective hydrogenation of cyclopentadienes to cyclopentene. It is a further object of this invention to employ this improved composition in the selective hydrogenation of dicyclopentadiene to at least one dihydrodicyclopentadiene. Other objects and advantages will be apparent from the detailed description and the appended claims. In accordance with this invention, a catalyst composition is provided which comprises, consists essentially of, or consists of (a) at least one palladium-containing material selected from the group consisting of palladium metal and palladium oxides, (b) at least one alkali metal iodide and (c) at least one inorganic support material. The inorganic support can be a spinel, alumina, silica, titania, zirconia, aluminosilicates, or mixtures of two or more thereof. In accordance with a second embodiment of this invention, a process which can be used for selectively hydrogenating a highly unsaturated hydrocarbon to a less unsaturated hydrocarbon is provided. The process comprises contacting a highly unsaturated hydrocarbon with hydrogen, in the presence of a catalyst composition, under a condition sufficient to effect a selective hydrogenation of the highly unsaturated hydrocarbon. The catalyst composition can be the same as the composition disclosed in the first embodiment of this invention. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 illustrates the advantages of an invention catalyst over a control catalyst in the selective hydrogenation of diolefins to monoolefins. FIG. 2 shows the selectivity to propylene in a selective hydrogenation of acetylene at different conversions of methylacetylene and propadiene. FIG. 3 shows the selectivity to C.sub.6 + hydrocarbons in a selective hydrogenation of acetylene at different conversions of methylacetylene and propadiene. DETAILED DESCRIPTION OF THE INVENTION As used in the present invention, the term "fluid" denotes gas, liquid, vapor, or combinations thereof. The term "saturated hydrocarbon" is referred to as any hydrocarbon which can be converted to an unsaturated hydrocarbon such as an olefinic compound by a thermal cracking process. An "unsaturated hydrocarbon" as used in this application is a hydrocarbon having at least one double bond between carbon atoms in the molecule. Generally, examples of saturated hydrocarbons include, but are not limited to, ethane, propane, butanes, pentanes, hexanes, octanes, decanes, naphtha, and combinations of any two or more thereof. Examples of unsaturated hydrocarbons include, but are not limited to, monoolefins such as ethylene, propylene, butenes, pentenes, hexenes, octenes, and decenes; aromatic compounds such as naphthalene; alkynes such as acetylene, propyne, and butynes; diolefins such as propadiene, butadienes, pentadienes (including isoprene), hexadienes, octadienes, and decadienes; and combinations of two or more thereof. The term "highly unsaturated hydrocarbon" refers to a hydrocarbon which contains a triple bond or two or more double bonds in a molecule. The termn "less unsaturated hydrocarbon" refer to a hydrocarbon in which the triple bond in the highly unsaturated hydrocarbon is hydrogenated to a double bond or a hydrocarbon in which the number of double bonds is one less than that in the highly unsaturated hydrocarbon. The term "selective hydrogenation" is referred to as a hydrogenation process which converts a highly unsaturated hydrocarbon such as an alkyne or a diolefin to a less unsaturated hydrocarbon such as a monoolefin without hydrogenating the less unsaturated hydrocarbon to a saturated or a more saturated hydrocarbon such as alkane. The composition of matter of this invention comprises, consists essentially of, or consists of component (a) palladium metal and/or at least one palladium oxide, component (b) at least one alkali metal iodide (preferably potassium iodide), and component (c) an inorganic support material selected from the group consisting of alumina, silica, titania, zirconia, aluminosilicates (clays and/or zeolites), zinc aluminate, zinc titanate, and combinations of two or more than two of these compounds, preferably alumina, more preferably alpha-alumina. Generally, the catalyst composition contains in the range of from about 0.01 weight-% palladium to about 2 weight-% palladium (Pd) (on a total catalyst composition weight basis) (preferably in the range of from about 0.05 weight-% Pd to about 1 weight-% Pd) and in the range of from about 0.02 weight-% alkali metal to about 10 weight-% alkali metal (on a total catalyst composition weight basis) (preferably in the range of from about 0.05 weight-% alkali metal to about 5 weight-% alkali metal) (preferably the alkali metal is potassium). The term "on a total catalyst composition weight basis" refers to the weight of the total catalyst composition. Thus, the weight-% of a component on a total catalyst composition weight basis is a percentage of the total catalyst composition weight. The composition of this invention may be characterized as a "skin catalyst." The composition of this invention is preferably in the form of catalyst particles. The term "skin" refers to the exterior surface of the composition which can contain components of the composition. The skin can be any thickness as long as such thickness can promote the selective hydrogenation disclosed herein. Generally, the thickness of the skin can be in the range of from about 1 micron to about 1000 microns, preferably in the range of from about 5 microns to about 750 microns, more preferably in the range of from about 5 microns to about 500 microns, and most preferably in the range from 10 microns to 300 microns. The catalyst hydrogenates more selectively when the skin is relatively thin (such as the most preferable skin thickness of 10 microns to 300 microns) than when then the skin is thicker (such as greater than 300 microns). Thus, there is a significant benefit, better selective hydrogenation, by preparing a composition with a thin skin, rather than a thick skin. Further, there is a significant benefit, better selective hydrogenation, by preparing a composition with a skin than a composition without a skin. As used in the present invention, the term "skin catalyst" denotes that at least about 40 weight-% of the Pd (on a Pd weight basis, thus the term "40 weight-% of the Pd" refers to 40 percent of the about 0.01 weight-% Pd (on a total catalyst composition weight basis) to about 2 weight-% Pd (on a total catalyst composition weight basis)), preferably at least about 45 weight-% of the Pd (on a Pd weight basis), is concentrated preferably within about 50 microns of the exterior surface of the composition. At least about 50 weight-% of the Pd (on a Pd weight basis), preferably at least about 55 weight-% of the Pd (on a Pd weight basis), is concentrated preferably within about 100 microns of the exterior surface of the composition. At least about 60 weight-% of the Pd (on a Pd weight basis), preferably at least about 65 weight-% of the Pd (on a Pd weight basis), is concentrated preferably within about 150 microns of the exterior surface of the composition. Preferably about 80 weight-% of the Pd (on a Pd weight basis), most preferably about 90 weight-% of the Pd (on a Pd weight basis), is concentrated in the skin of the composition, preferably in an area within about 300 microns of the exterior surface of the composition. Various skin catalysts have been developed. See for example U.S. Pat. No. 4,404,124 and U.S. Pat. No. 4,484,015, disclosures of which are incorporated herein by reference. One can use any suitable method to determine the concentration of the palladium in the skin of the composition. One technique currently favored is the electron microprobe which is well known to one skilled in the art. Another technique involves breaking open a representative sample of the composition (in catalyst particle form) and treating the catalyst particles with a dilute alcoholic solution of N,N-dimethyl-para-nitrosoaniline. The treating solution reacts with the palladium to give a red color which can be used to evaluate the distribution of the palladium. Another technique for measuring the concentration of the palladium in the skin of the composition involves breaking open a representative sample of catalyst particles followed by treatment with a reducing agent such as, for example hydrogen, to change the color of the skin to evaluate the distribution of the palladium. The catalyst particles can be of any suitable shape (spherical, cylindrical, trilobal and the like), and are preferably either spherical pellets or cyclindrical extrudates. The catalyst particles can be of any suitable dimension and particle size (diameter/length) and generally have a size in the range of from about 1 mm to about 10 mm. However, the advantages of the skin type catalyst are particularly notable for those particles having minimum dimensions of at least about 1 millimeter. A particularly suitable form of catalyst particle is one having dimensions in the range of from about 2 to about 6 millimeters. The catalyst particles can have any suitable surface area (measured by the BET method by Brunauer, Emmett and Teller employing N.sub.2), and generally have a surface area in the range of from about 1 m.sup.2 /g to about 200 m.sup.2 /g (preferably in the range of from about 5 m.sup.2 /g to about 100 m.sup.2 /g). The catalyst particles can be prepared by any suitable means which results in the palladium concentrated in the exterior surface skin of the catalyst particles with the alkali metal iodide distributed in the skin or throughout the catalyst particles. Generally, the extent of penetration of the palladium into the skin of the catalyst particles can be controlled by adjustment of the acidity of the promoter-component containing solution with an acid such as, for example, hydrochloric acid. For example, if the promoter-component containing solution is palladium chloride (PdCl.sub.2), hydrochloric acid should be added to such promoter-component containing solution to form a PdCl.sub.4.sup.-2 complex. Excess hydrochloric acid should be avoided. The promoter components (a) palladium metal and/or at least one palladium oxide, and (b) at least one alkali metal iodide (preferably potassium iodide) can be deposited onto and/or incorporated into the inorganic support material by any suitable means and in any suitable order. It has been discovered that the combination of silver or silver-containing compounds with at least one alkali metal iodide (along with components (a) and (c)) results in a composition that is less effective in selective hydrogenation than the present inventive composition which does not contain a substantial concentration of silver or silver-containing compounds. Thus, it is preferred that the inventive composition contain no substantial concentration of silver or silver-containing compounds especially a substantial concentration such that there is a significant effect on the selective hydrogenation capabilities of the inventive catalyst composition. There is a significant effect on the selective hydrogenation capabilities of the inventive catalyst composition when 40 weight percent (on a total feed weight basis) fewer highly unsaturated hydrocarbons (preferably 30 weight percent fewer highly unsaturated hydrocarbons, most preferably 20 weight percent fewer highly unsaturated hydrocarbons) are converted to less unsaturated hydrocarbons during selective hydrogenation using the inventive catalyst composition than when a composition contains a substantial concentration of silver or silver-containing compounds. Most preferably, the inventive catalyst composition does not contain silver or silver-containing compounds. While the palladium and alkali metal iodide containing composition (final catalyst composition) may be heated or calcined in an oxidizing gas atmosphere such as air at temperatures less than about 200.degree. C., the final composition should not be heated or calcined in an oxidizing gas atmosphere at temperatures greater than about 200.degree. C. Heating or calcining the final composition in an oxidizing gas atmosphere at temperatures greater than about 200.degree. C. will result in the iodide being driven off in the form of gaseous iodine rendering the final composition unuseful for the selective hydrogenation disclosed herein. For instance, the alkali metal iodide can be incorporated into the support material, by impregnation, followed by impregnation of the alkali metal iodide-containing support material with at least one Pd compound (such as H.sub.2 PdCl.sub.4) to obtain an alkali metal iodide-impregnated material, drying the alkali metal iodide-impregnated material to obtain a dried material, and then heating (calcining) of the dried material (preferably in a non-oxidizing or reducing gas atmosphere such as hydrogen gas, or in an inert gas atmosphere such as nitrogen, helium and the like and combinations thereof) to obtain the final catalyst composition. Or, a supported palladium catalyst composition, preferably a Pd/Al.sub.2 O.sub.3 composition (more preferably one which is commercially available, e.g., from Mallinckrodt Specialty Chemicals Company, Erie, Pa.), can be impregnated with an alkali metal iodide to obtain an alkali metal iodide-impregnated material, followed by drying the alkali metal iodide-impregnated material to obtain a dried material, and then heating the dried material (preferably in a non-oxidizing or reducing or inert gas atmosphere) to obtain the final catalyst composition. Or, the supported palladium catalyst composition can be impregnated with at least one alkali metal iodate to obtain an alkali metal iodate-impregnated material, followed by drying the alkali metal iodate-impregnated material to obtain a dried material, and then heating the dried material in a non-oxidizing or reducing gas atmosphere, preferably hydrogen gas (at a temperature sufficient to convert the alkali metal iodate to alkali metal iodide) to obtain the final catalyst composition. The preferred starting material (also referred to as "base catalyst"), which is to be improved in accordance with this invention by incorporation of alkali metal iodide thereon or therein, can be any supported palladium-containing composition having the palladium concentrated in the skin of the composition. The base catalyst composition can be a fresh hydrogenation catalyst or it can be a used and thereafter regenerated hydrogenation catalyst composition. Broadly, the base catalyst can contain about 0.01 weight-% Pd (on a total catalyst composition weight basis) to about 2 weight-% Pd (preferably about 0.05 weight-% Pd to about 1 weight-% Pd), and a solid inorganic support material (listed above), preferably alumina (more preferably alpha-alumina). The supported Pd-containing base catalyst particles can have any suitable shape, and preferably are spherical pellets or cylindrical extrudates. The size of these supported base catalyst particles generally is in the range of from about 1 mm to about 10 mm, preferably in the range of from about 2 mm to about 6 mm, and its surface area generally is in the range of from about 1 m.sup.2 /g to about 200 m.sup.2 /g. In one preferred method of preparing the catalyst composition of this invention, a Pd-containing base catalyst (described above), which more preferably has been prereduced with hydrogen gas at room temperature (about 10.degree. C. to about 40.degree. C.), is contacted with a solution (preferably aqueous) of at least one alkali metal iodide (preferably KI) at such conditions as to obtain a final catalyst composition containing in the range of from about 0.02 weight-% of alkali metal (on a total catalyst composition weight basis) to about 10 weight-% of alkali metal (preferably in the range of from about 0.05 weight-% of alkali metal to about 5 weight-% of alkali metal) (preferably, the alkali metal is potassium). Generally, the concentration of the alkali metal iodide in the contacting (impregnating) solution (preferably aqueous) is in the range of from about 0.02 mol/l to about 10 mol/l (preferably in the range of from about 0.2 mol/l to about 3 mol/l). The preferred contacting method is "incipient wetness impregnation," i.e., essentially completely filling the pores of the base catalyst with the alkali metal iodide solution. Generally, the weight ratio of the solution to the solid base catalyst composition is in the range of from about 0.2:1 to about 2:1, preferably in the range of from about 0.4:1 to about 1:1 (depending on the alkali metal iodide concentration of the impregnating solution and the desired alkali metal iodide level to be attained in the catalyst composition of this invention). Thereafter, the impregnated catalyst composition is substantially dried (preferably at about 50.degree. C. to about 150.degree. C. for about 0.5 hour to about 20 hours) and heated in a non-oxidizing gas atmosphere (more preferably in a reducing gas such as H.sub.2, or an inert gas such as N.sub.2, He and the like and combinations thereof) at a temperature in the range of from about 300.degree. C. to about 600.degree. C. (preferably in the range of from about 300.degree. C. to about 500.degree. C.) for a time period in the range of from about 0.2 hour to about 20 hours (preferably in the range of from about 1 hour to about 10 hours). In another preferred method of preparing the catalyst composition of this invention, a Pd-containing base catalyst (described above) is contacted with a solution (preferably aqueous) of at least one alkali metal iodate (preferably KIO.sub.3) at such conditions to obtain a final catalyst composition containing in the range of from about 0.02 weight-% alkali metal (on a total catalyst composition weight basis) to about 10 weight-% alkali metal (preferably in the range of from about 0.05 weight-% alkali metal to about 5 weight-% alkali metal) (preferably, the alkali metal is potassium), wherein the concentration of the alkali metal iodate(s) in the impregnating solution is in the range of from about 0.02 mol/l to about 10 mol/l (preferably in the range of from about 0.2 mol/l to about 3 mol/l). The impregnating procedure is carried out essentially in accordance with the method described above for the impregnation with alkali metal iodide. Thereafter, the impregnated catalyst composition is substantially dried (as described above) and heated in a reducing gas (preferably H.sub.2) at a temperature in the range of from about 200.degree. C. to about 600.degree. C. (preferably in the range of from about 300.degree. C. to about 500.degree. C.) for a time period in the range of from about 0.2 hour to about 20 hours (preferably in the range of from about 1 hour to about 10 hours) so as to convert said at least one alkali metal iodate to at least one alkali metal iodide. In another preferred method of preparing the catalyst composition of this invention, the impregnated catalyst material is dried and heated (as described above) and then treated with one or more sulfur-containing compounds such as sulfides, disulfides, mercaptans, mercaptides, thiophenes, thiophanes, thiophenols, benzothiophenes, dibenzothiophenes and the like and combinations thereof. The presently preferred sulfur-containing compound is thiophene. The total amount of sulfur in the one or more sulfur-containing compounds is preferably about 100 parts-per-million (ppm) sulfur, more preferably about 75 ppm sulfur, and most preferably 50 ppm sulfur. Any suitable means known to one skilled in the art may be used to treat the dried and heated impregnated catalyst composition with the one or more sulfur-containing compounds. One preferred method is by soaking the dried and heated impregnated catalyst composition at about room temperature (approximately in the range of from about 20.degree. C. to about 25.degree. C.) for a time period in the range of from about 5 hours to about 20 hours (preferably in the range of from about 10 hours to about 18 hours) in a sulfur-compound-containing solution such as thiophene containing about 30 ppm sulfur. The selective hydrogenation process of this invention can be carried out by contacting a fluid which comprises a highly unsaturated hydrocarbon, in the presence of hydrogen, with the catalyst composition disclosed above. Preferably the fluid containing a highly unsaturated hydrocarbon is or comprises an unsaturated alkene stream containing an alkyne, a diolefin, or both as an impurity, generally at a level in the range of from about 1 mg/Kg (ppm) to about 50,000 ppm of the fluid. The unsaturated alkene in the fluid can be ethylene, propylene, butenes, or combinations of two or more thereof. The highly unsaturated hydrocarbon can be, for example, an alkyne, a diolefin, or combinations of any two or more thereof. Examples of suitable alkynes include, but are not limited to, acetylene, propyne, 1-butyne, 2-butyne, 1-pentyne, 2-pentyne, 3-methyl-1-butyne, 1-hexyne, 1-heptyne, 1-octyne, 1-nonyne, 1-decyne, and mixtures of two or more thereof. The presently preferred alkyne is acetylene. These alkynes are primarily hydrogenated to the corresponding alkenes. For example, acetylene is primarily hydrogenated to ethylene, propyne is primarily hydrogenated to propylene, and the butynes are primarily hydrogenated to the corresponding butenes (1-butene, 2-butenes). Similarly, in the selective hydrogenation of diolefins, the diolefins are hydrogenated to the corresponding monoolefins such as, for example, 1,3-butadienes are selectively hydrogenated to butenes. The catalyst composition of this invention can be employed directly in the selective hydrogenation process of the second embodiment of this invention. However, it is preferred to first treat the catalyst composition with a reducing gas such as hydrogen. Generally, the optimal operation of the selective hydrogenation does not begin until there has been a substantial reduction of the palladium component. Typically, the reduction can be carried out at a temperature in the range of from about 10.degree. C. to about 200.degree. C., preferably in the range of from about 20.degree. C. to 100.degree. C., for at least about 10 minutes, preferably in the range of from about 0.5 hour to about 10 hours, and most preferably in the range of from 1 hour to 10 hours. Non-limiting examples of suitable diolefins, preferably containing 3 to 12 carbon atoms per molecule which can be hydrogenated in the process of this invention, include propadiene, 1,2-butadiene, 1,3-butadiene, isoprene, 1,2-pentadiene, 1,3-pentadiene, 1,4-pentadiene, 1,2-hexadiene, 1,3-hexadiene, 1,4-hexadiene, 1,5-hexadiene, 2-methyl-1,2-pentadiene, 2,3-dimethyl-1,3-butadiene, heptadienes, methylhexadienes, octadienes, methylheptadienes, dimethylhexadienes, ethylhexadienes, trimethylpentadienes, methyloctadienes, dimethylheptadienes, ethyloctadienes, trimethylhexadienes, nonadienes, decadienes, undecadienes, dodecadienes, cyclopentadienes, cyclohexadienes, methylcyclopentadienes, cycloheptadienes, methylcyclohexadienes, dimethylcyclopentadienes, ethylcyclopentadienes, dicyclopentadiene, and mixtures of one or two of these diolefins. Presently preferred diolefins are propadiene, 1,3-butadiene, pentadienes (such as 1,3-pentadiene, 1,4-pentadiene, isoprene), cyclopentadienes (such as 1,3-cyclopentadiene) and dicyclopentadiene (also known as tricyclo[5.2.1].sup.2,6 deca-3,8-diene). These diolefins are selectively hydrogenated to the monoolefins containing the same number of carbon atoms per molecule as the diolefins. For example, 1,3-butadiene is hydrogenated to 1-butene and 2-butene, 1,3-pentadiene and 1,4-pentadiene are hydrogenated to 1-pentene and 2-pentene, isoprene is hydrogenated to methyl-1-pentenes and methyl-2-pentenes, 1,3-cyclopentadiene is hydrogenated to cyclopentene, and dicyclopentadiene is hydrogenated to dihydrocyclopentadienes (in particular, tricyclo[5.2.1].sup.2,6 dec-3-ene). The highly unsaturated hydrocarbon-containing fluid feed for the hydrogenation process of this invention can also comprise other hydrocarbons, in particular, monoolefins and aromatic hydrocarbons. Non-limiting examples of such other hydrocarbons which can be present in the feed at a level of at least 30 volume-% include, but are not limited to, ethylene, propylene, 1-butene, 2-butene, isobutylene, 1-pentene, 2-pentene, methyl-1-butenes (such as 2-methyl-1-butene), methyl-2-butenes (such as 2-methyl-2-butene), 1-hexene, 2-hexene, 3-hexene, methyl-1-pentenes, 2,3-dimethyl-1-butene, 1-heptene, 2-heptene, 3-heptene, methyl-1-hexenes, methyl-2-hexenes, methyl-3-hexenes, dimethylpentenes, ethylpentenes, octenes, methylheptenes, dimethylhexenes, ethylhexenes, nonenes, methyloctenes, dimethylheptenes, ethylheptenes, trimethylhexenes, cyclopentene, cyclohexene, methylcyclopentene, cycloheptene, methylcyclohexene, dimethylcyclopentenes, ethylcyclopentenes, cyclooctenes, methylcycloheptenes, dimethylcyclohexenes, ethylcyclohexenes, trimethylcyclohexenes, methylcyclooctenes, dimethylcyclooctenes, ethylcylcooctenes, benzene, toluene, ethylbenzene, styrene, xylenes and the like, and mixtures of two or more than two of these hydrocarbons. The fluid feed, which may be liquid or gaseous at the hydrogenating conditions of this process, generally comprises in the range of from about 0.1 weight-% of at least one diolefin to about 99.9 weight-% of at least one diolefin. The fluid feed can additionally comprise other hydrocarbons (at a level in the range of from about 0.1 weight-% to about 99.9 weight-%), in particular aromatic hydrocarbons, such as benzene, toluene, styrene and ethylbenzene, which may be present at a level in the range of from about 50 weight-% to about 99 weight-%. However, it is within the scope of this invention to employ feeds which contain about 100% of at least one diolefin, such as substantially pure dicyclopentadiene. Also, the feed can contain small amounts, generally less than about 0.05 weight %, in particular in the range of from about 10 ppm S to about 400 ppm S, of sulfur compounds (such as H.sub.2 S, carbonyl sulfide, carbon disulfide, mercaptans, organic sulfides such as thiophene, organic di-, tri- and tetrasulfides, and the like) as impurities. Carbon monoxide and/or water (generally less than about 0.05 mole-% of each) can also be present as impurities. The selective hydrogenation process of this invention is generally carried out by contacting a feed stream containing at least one highly unsaturated hydrocarbon and molecular hydrogen with the catalyst of this invention which is generally contained in a fixed bed. Generally, in the range of from about 1 to about 10, preferably in the range of from about 1 to about 2, moles of hydrogen are employed for each mole of the highly unsaturated hydrocarbon present in the feed. The temperature necessary for the selective hydrogenation process of this invention depends largely upon the activity of the catalyst and the desired extent of diolefin hydrogenation. Generally, reaction temperatures in the range of from about 10.degree. C. to about 300.degree. C., preferably in the range of from about 20.degree. C. to about 250.degree. C., and most preferably 30.degree. C. can be used. A suitable reaction pressure generally is in the range of from about 15 pounds per square inch gauge (psig) to about 2,000 pounds per square inch gauge (psig), preferably in the range of from about 50 psig to about 1,500 psig, and most preferably in the range of from 100 psig to 1,000 psig. The liquid hourly space velocity (LHSV) of the hydrocarbon feed can vary over a wide range. Typically, the space velocity of the feed will be in the range of from about 0.5 liter of hydrocarbon feed per liter of catalyst per hour (liter/liter/hour) to about 100 liters of hydrocarbon feed per liter of catalyst per hour, more preferably in the range of from about 2 liters/liter/hour to about 60 liters/liter/hour. The hydrogenation process conditions should be such as to avoid significant hydrogenation of monoolefins which are formed by hydrogenation of the highly unsaturated hydrocarbons being initially present in the feed to saturated hydrocarbons such as alkanes and cycloalkanes. In a preferred embodiment, the at least one alkadiene is selected from the group consisting of propadiene, 1,3-butadiene, 1,3-pentadiene, 1,4-pentadiene and isoprene and is selectively hydrogenated with hydrogen gas to at least one alkene selected from the group consisting of butenes and pentenes in the presence of the catalyst composition of this invention. In another preferred embodiment, 1,3-cyclopentadiene is selectively hydrogenated with hydrogen gas to cyclopentene in the presence of the catalyst composition of this invention. In still another preferred embodiment, dicyclopentadiene is selectively hydrogenated with hydrogen gas to at least one dihydrodicyclopentadiene in the presence of the catalyst composition of this invention. In one of the preferred embodiments of the diolefin hydrogenation process of this invention, a feed stream containing at least one pentadiene, such as, for example, 1,3-pentadiene and/or 1,4-pentadiene and/or isoprene and molecular hydrogen is contacted with the catalyst, generally contained in a fixed bed. Generally, the hydrocarbon feed contains other hydrocarbons, such as C.sub.4 + alkanes (butanes, pentanes, hexanes), C.sub.4 + alkenes (butenes, pentenes, hexenes) and aromatic hydrocarbons (benzene, toluene, ethylbenzene, styrene and the like). This preferred hydrogenation process generally employs in the range of from about 1 moles of H.sub.2 per mole of pentadiene(s) to about 2 moles of H.sub.2 per mole of pentadiene(s). The reaction temperature necessary for the selective hydrogenation of pentadiene depends largely upon the activity of the catalyst and the desired extent of the pentadiene hydrogenation, and generally is in the range of from about 35.degree. C. to about 100.degree. C. Generally, the total pressure is in the range of from about 50 pounds per square inch gauge (psig) to about 1,000 pounds per square inch gauge (psig). The liquid hourly space velocity (LHSV) of the hydrocarbon feed can also vary over a wide range. Typically, the liquid hourly space velocity will be in the range of from about 1 liter of hydrocarbon feed per liter of catalyst per hour (liters/liter/hour) to about 50 liters/liter/hour. The hydrogenation process conditions should be such as to avoid significant hydrogenation of pentenes to pentane. In another preferred embodiment, dicyclopentadiene is selectively hydrogenated to dihydrodicyclopentadienes, mainly the dicyclopentene containing the double bond in the "3" position (i.e., tricyclo[5.2.1].sup.2,6 dec-3-ene). In still another preferred embodiment, 1,3-butadiene is selectively hydrogenated to butenes. Operating conditions for these embodiments are substantially the same as those described above for the selective hydrogenation of pentadiene(s) to pentenes. Also within the scope of this invention is to employ the catalyst composition in accordance with this invention for the selective hydrogenation of alkynes, preferably containing 2 to 12 carbon atoms, to the corresponding monoolefins (alkenes). The reaction conditions for the selective alkyne hydrogenation are approximately the same as those described above for the selective hydrogenation of diolefins to monoolefins. If it is desired to regenerate the catalyst of this invention after prolonged use in a hydrogenation process, this can be accomplished by leaching the spent catalyst with water to dissolve the alkali metal iodide, calcining the leached catalyst in an oxidizing atmosphere (e.g., in air; at a temperature in the range of from about 500.degree. C. to about 600.degree. C.) to burn off carbonaceous deposits, reimpregnating the calcined catalyst with dissolved alkali metal iodide, and heating it (as is described for the fresh catalyst of this invention). The following examples are presented to further illustrate this invention and should not be construed as unduly limiting the scope of this invention. |
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