Process for preparing alcohols by the Oxo process

Abstract

An improved process for preparing alcohols by the Oxo process. More particularly this invention relates to an improvement in the hydrogenation step of the Oxo process characterized in the use of certain bulk multimetallic hydrogenation catalysts comprised of at least one Group VIII non-noble metal and at least two Group VIB metals.

Description

FIELD OF THE INVENTION

This invention relates to an improved process for preparing alcohols by the Oxo process. More particularly, this invention relates to an improvement in the hydrogenation step of the Oxo process characterized in the use of certain bulk multimetallic hydrogenation catalysts comprised of at least one Group VIII non-oble metal and at least two Group VIB metals.

BACKGROUND OF THE INVENTION

The Oxo process is well known in the art and is generally described in detail in Kirk-Othmer, Encyclopedia of Chemical Technology, Volume 16, 3rd ed., John Wiley & Sons, pp. 637-653, 1981.

In the well known Oxo process, olefins are hydroformylated by reaction with carbon monoxide and hydrogen, generally charged as synthesis gas (syn gas) mixtures, in the presence of a cobalt Oxo catalyst in dissolved form to form a mixture of Oxo aldehydes and alcohols. This Oxo reaction is typically carried out at syn gas pressures of from about 10.33 MPa to 31.00 MPa (1500 to 4500 psig) and at temperatures of from about 65° C. to 230° C. Thereafter, the product mixture containing the alcohols and aldehydes is recovered and can then be treated by known means to hydrogenate the aldehydes to form additional quantities of the corresponding alcohols. These alcohols, in turn, are widely used as chemical intermediates in the manufacture of plasticizers, detergents, solvents, and the like.

Prior to the hydrogenation step, the crude Oxo reaction effluent, which contains dissolved cobalt catalysts, the aldehyde and alcohol products and reaction by-products together with any metallic contaminants, is generally treated to remove the dissolved cobalt catalyst, which then for reasons of economy must be recycled to the Oxo reactor.

“Demetalled” hydroformylation reaction product or crude Oxo alcohol product is the reaction product which is substantially depleted of the transition metal cobalt catalyst required for the hydroformylation reaction. Such crude Oxo product will generally contain cobalt in an amount of from about 0.05 to 3.0 wt. %, calculated as elemental cobalt. The concentration of aldehyde in the crude Oxo alcohol product is generally from about 20 to 75 wt. %.

The next step in the Oxo process is the hydrogenation of the crude alcohol product which is typically carried out at pressures of about 4.83 MPa to 31.00 MPa (700 to 4500 psig) using sulfided bimetallic cobalt and molybdenum oxides or nickel and molybdenum oxide supported on alumina as the hydrogenation catalyst. Because of the high content of carbonyl-containing compounds present in the crude alcohol product the use of relatively high pressures with the traditional bimetallic catalysts has been required in order to achieve the desired yield of alcohol product.

The use of bimetallic catalysts in the hydrogenation of crude alcohol Oxo product is disclosed, for example, U.S. Pat. No. 5,030,774, issued Jul. 9, 1991, and European Application 89304856.1, published Nov. 29, 1989. The present invention is based on the discovery that certain multimetallic catalysts are useful in the two separate hydrogenation steps practiced in the cobalt catalyzed Oxo process.

A parallel Rhodium catalyzed Oxo process is known in the art. The rhodium oxo process employes various catalyst forms including ligand-modified rhodium, rhodium modified with ionic phosphine ligands, and unmodified rhodium catalyst. The ligand-modified rhodium hydroformylation process is typically carried out at low pressures [0.7-3 MPa (100-450 psi)] and low temperatures (80° C.-120° C.). The ionic phosphine ligand process is typically carried out at higher temperatures greater than 125° C. and pressures in excess of 6 MPa. The Rhodium oxo process is discussed in Kirk-Othmer, Encyclopedia of Chemical Technology, Volume 17, 4th ed., John Wiley & Sons, pp. 902-919, 1996, the entirety of which is hereby incorporated by reference.

SUMMARY OF THE INVENTION

In accordance with the present invention there has been discovered an improvement in the process for preparing Oxo alcohols by the catalyzed hydroformylation of olefins which comprises the steps of:

(a) hydroformylation of a hydrocarbon stream comprising at least one olefin selected from C 4 , C 5 , C 6 , C 7 , C 8 , C 9 , C 10 , C 11 , and C 12 olefins by reaction of said olefin with carbon monoxide and hydrogen in the presence of a hydroformylation catalyst to produce a crude reaction product which contains carbonyl-containing compounds;

(b) optionally, demetalling the crude reaction product of step (a) to recover therefrom homogeneous hydroformylation catalyst and to separate therefrom essentially hydroformylation catalyst-free crude alcohol product which contains 20 wt. % or more of said carbonyl-containing compounds;

(c) hydrogenating said crude alcohol product of step (b) to reduce at least a portion of said carbonyl-containing compounds to alcohols;

(d) optionally, distilling the product of step (c) and recovery therefrom Oxo alcohols containing a reduced amount of said carbonyl-containing compounds; and

(e) optionally, hydrofinishing (by hydrogenation) the product of step (d) to provide a substantially pure alcohol product; the improvement which comprises conducting step (c) or step (e) or both in the presence of a bulk multimetallic catalyst comprised of at least one Group VIII non-noble metal and at least two Group VIB metals, wherein the ratio of Group VIB to Group VIII metals is from about 10:1 to about 1:10.

In a preferred embodiment the hydroformylation catalyst is selected from a rhodium-containing catalyst and a cobalt-containing catalyst. In a preferred embodiment the hydroformylation catalyst is a cobalt carbonyl catalyst.

In a preferred embodiment of the present invention the Group VIII non-noble metal is selected from Ni and Co and the Group VIB metals are selected from Mo and W.

In another preferred embodiment of the present invention two Group VIB metals are present as Mo and W and the ratio of Mo to W is about 9:1 to about 1:9.

In yet another preferred embodiment of the present invention the bulk multimetallic is represented by the formula:

(X) b (Mo) c (W) d O Z

wherein X is a Group VIII non-noble metal, and the molar ratio of b: (c+d) is 0.5/1 to 3/1, preferably 0.75/1 to 1.5/1, more preferably 0.75/1 to 1.25/1.

In still another preferred embodiment of the present invention the molar ratio of c:d is preferably >0.01/1, more preferably >0.1/1, still more preferably 1/10 to 10/1, still more preferably 1/3 to 3/1, most preferably substantially equimolar amounts of Mo and W, e.g., 2/3 to 3/2; and z=[2b+6(c+d)]/2.

In another preferred embodiment of the present invention the essentially amorphous material has a unique X-ray diffraction pattern showing crystalline peaks at d=2.53 Angstroms and d=1.70 Angstroms.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 is the X-ray diffraction pattern of a NH 4 —Ni-0.5Mo-0.5W-O compound prepared by boiling precipitation before calcining (Curve A) and after calcining at 400° C. (Curve B). Note that the patterns for both the precursor and the decomposition product of the precursor are quite similar with the two peaks at essentially the same place. The ordinate is relative intensity; the abscissa is two theta (degrees).

FIG. 2 shows the X-ray diffraction patterns, by CuKα radiation (λ=1.5405Å), of NH 4 —Ni—Mo 1−x —W x —O precursors wherein curve A is Mo 0.9 W 0.1 , curve B is Mo 0.7 W 0.3 , curve C is Mo 0.5 W 0.5 , curve D is Mo 0.3 Wo 0.7 , curve E is Mo 0.1 W 0.9 , and curve F is Mo 0 W 1 . The ordinate and abscissa are as described for FIG. 1 .

DETAILED DESCRIPTION OF THE INVENTION

As used herein and in the claims, the term “carbonyl-containing compounds” refers to any hydrocarbon compound containing at least one carbon atom doubly bonded to an oxygen atom. Carbonyl-containing compounds includes, but is not limited to, aldehydes, acetals, carboxylic acids, ketones, ethers, and esters.

The olefin feedstock for the hydroformylation reaction is typically a commercial olefin feedstock which may include linear and branched C 2 -C 17 monoolefins. Preferably, the olefin feedstock contains a significant amount of a branched C 5 -C 12 monoolefin. The preferred olefins include amylenes from petroleum cracking, heptenes, octenes, nonenes and dodecenes from fractionation of oligomers of C 3 -C 4 olefin, and octenes from dimerization and codimerization of isobutylene and 1- and 2-butenes.

Cobalt catalyzed hydroformylation is typically carried out at a pressure of 15-30 MPa and a temperature of about 120° C.-190° C. Cobalt catalyst is present in its active form as hydrido cobalt carbonyl in a concentration of from 0.05-3.0 wt. %, preferably 0.05 to wt. %, calculated as metal based on olefin feedstock. The synthesis gas typically has a H 2 :CO volume ratio in the range of 0.9:1 to 1.5:1.

After separation of the cobalt catalyst from the crude reaction product the crude alcohol product, which is hydrogenated in accordance with this invention, will contain a substantial proportion of carbonyl-containing compounds which are produced as a result of the hydroformylation reaction. These carbonyl-containing compounds mainly include aldehydes, acetals, formates, esters and ethers, and the crude alcohol product will contain 20 wt % or more, more typically 40 to 60 wt. %, of aldehydes and other carbonyl compounds which are to be hydrogenated to the desired alcohol product.

The catalysts of the present invention may be used either in the first hydrogenation step of the Oxo process or in the final hydrofinishing (hydrogenation) step, or in both. When used in the first hydrogenation step, the expected advantage will result in enabling this step to be carried out at relatively lower pressures, i.e., less than 10.34 MPa (1500 psig) and/or a relatively lower temperature, i.e., less than 160° C. while still achieving a desired conversion of carbonyl-containing compounds to the alcohol product. When used as the catalyst in the final hydrofinishing step, which is also a hydrogenation reaction, its expected advantage is that the carbonyl number (mg KOH/g) may be effectively reduced to levels less than 0.2 mg KOH/g in the finished alcohol product. It is expected that use of the trimetallic catalysts of the invention in the hydrofinishing step will provide the desired carbonyl numbers at superior conversion rates when compared with bimetallic catalysts. The hydrofinishing step is preferably carried out at about 5.51 MPa (800 psig) and 130° C. (266° F.), this step effects trace removal of carbonyl species by hydrogenation.

The hydrogenation catalysts of the present invention may also be used in the corresponding crude alcohol hydrotreating step of the rhodium catalyzed Oxo process. Additionally, the hydrogenation catalyst of the present invention may be used in the hydrofinishing step of the rhodium catalyzed oxo process. The rhodium catalyzed oxo process is well known in the art. The rhodium oxo process employs various catalyst forms including ligand-modified rhodium, rhodium modified with ionic phosphine ligands, and unmodified rhodium catalyst. The ligand-modified rhodium hydroformylation process is typically carried out at low pressures [0.7-3 MPa (100-450 psi)] and low temperatures (80-120° C.). The ionic phosphine ligand process is typically carried out at higher temperatures greater than 125° C. and pressures in excess of 6 MPa. The Rhodium oxo process is discussed in Kirk-Othmer, Encyclopedia of Chemical Technology, Volume 17, 4th ed., John Wiley & Sons, pp. 902-919, 1996, the entirety of which is hereby incorporated by reference.

The catalysts used in the practice of this invention are bulk multimetallic catalysts comprised of at least one Group VIII non-noble metal and at least two Group VIB metals and wherein the ratio of Group VIB metal to Group VIII non-noble metal is from about 10:1 to about 1:10. It is preferred that the catalyst be a bulk trimetallic catalyst comprised of one Group VIII non-noble metal, preferably Ni or Co and the two Group VIB metals Mo and W. It is preferred that the ratio of Mo to W be about 9:1 to about 1:9.

The preferred bulk trimetallic catalyst compositions used in the practice of the present invention is represented by the formula:

(X) b (Mo) c (W) d O z

wherein X is a Group VIII non-noble metal, the molar ratio of b: (c+d) is 0.5/1 to 3/1, preferably 0.75/1 to 1.5/1, more preferably 0.75/1 to 1.25/1;

The molar ratio of c:d is preferably >0.01/1, more preferably >0.1/1, still more preferably 1/10 to 10/1, still more preferably 1/3 to 3/1, most preferably substantially equimolar amounts of Mo and W, e.g., 2/3 to 3/2; and z=[2b +6 (c+d)]/2.

The essentially amorphous material has a unique X-ray diffraction pattern showing crystalline peaks at d=2.53 Angstroms and d=1.70 Angstroms. The mixed metal oxide is readily produced by the decomposition of a precursor having the formula:

(NH 4 ) a (X) b (Mo) c (W) d O z

wherein X is a Group VIII non-noble metal, the molar ratio of a:b is ≦1.0/1, preferably 0-1; and b, c, and d, are as defined above, and z=[a+2b+6 (c+d)]/2. The precursor has similar peaks at d=2.53 and 1.70 Angstroms.

Decomposition of the precursor may be effected at elevated temperatures, e.g., temperatures of at least about 300° C., preferably about 300-450° C., in a suitable atmosphere, e.g., inerts such as nitrogen, argon, or steam, until decomposition is substantially complete, i.e., the ammonium is substantially completely driven off. Substantially complete decomposition can be readily established by thermogravimetric analysis (TGA), i.e., flattening of the weight change curve.

The catalyst compositions used in the practice of the present invention can be prepared by any suitable means. One such means is a method wherein not all of the metals are in solution. Generally, the contacting of the metal components in the presence of the protic liquid comprises mixing the metal component and subsequently reacting the resulting mixture. It is essential to the solid route that at least one metal component is added at least partly in the solid state during the mixing step and that the metal of at least one of the metal components which have been added at least partly in the solid state, remains at least partly in the solid state during the mixing and reaction step. “Metal” in this context does not mean the metal in its metallic form but present in a metal compound, such as the metal component as initially applied or as present in the bulk catalyst composition.

Generally, during the mixing step either at least one metal component is added at least partly in the solid state and at least one metal component is added in the solute state, or all metal components are added at least partly in the solid state, wherein at least one of the metals of the metal components which are added at least partly in the solid state remains at least partly in the solid state during the entire process of the solid route. That a metal component is added “in the solute state” means that the whole amount of this metal component is added as a solution of this metal component in the protic liquid. That a metal component is added “at least partly in the solid state” means that at least part of the metal component is added as solid metal component and, optionally, another part of the metal component is added as a solution of this metal component in the protic liquid. A typical example is a suspension of a metal component in a protic liquid in which the metal is at least partly present as a solid, and optionally partly dissolved in the protic liquid.

To obtain a bulk catalyst composition with high catalytic activity, it is therefore preferred that the metal components, which are at least partly in the solid state during contacting, are porous metal components. It is desired that the total pore volume and pore size distribution of these metal components is approximately the same as those of conventional hydrotreating catalysts. Conventional hydrotreating catalysts generally have a pore volume of 0.05-5 ml/g, preferably of 0.1-4 ml/g, more preferably of 0.1-3 ml/g and most preferably of 0.1-2 ml/g determined by nitrogen adsorption. Pores with a diameter smaller than 1 nm are generally not present in conventional hydrotreating catalysts. Further, conventional hydrotreating catalysts have generally a surface area of at least 10 m 2 /g and more preferably of at least 50 m 2 /g and most preferably of at least 100 m 2 /g, determined via the BET method. For instance, nickel carbonate can be chosen which has a total pore volume of 0.19-0.39 ml/g and preferably of 0.24-0.35 ml/g determined by nitrogen adsorption and a surface area of 150-400 m 2 /g and more preferably of 200-370 m 2 /g determined by the BET method. Furthermore these metal components should have a median particle diameter of at least 50 nm, more preferably at least 100 nm, and preferably not more than 5000 μm and more preferably not more than 3000 μm. Even more preferably, the median particle diameter lies in the range of 0.1-50 μm and most preferably in the range of 0.5-50 μm. For instance, by choosing a metal component which is added at least partly in the solid state and which has a large median particle diameter, the other metal components will only react with the outer layer of the large metal component particle. In this case, so-called “core-shell” structured bulk catalyst particles are obtained.

An appropriate morphology and texture of the metal component can either be achieved by applying suitable preformed metal components or by preparing these metal components by the above-described precipitation under such conditions that a suitable morphology and texture is obtained. A proper selection of appropriate precipitation conditions can be made by routine experimentation.

As has been set out above, to retain the morphology and texture of the metal components which are added at least partly in the solid state, it is essential that the metal of the metal component at least partly remains in the solid state during the whole process of this solid route. It is noted again that it is essential that in no case should the amount of solid metals during the process of the solid route becomes zero. The presence of solid metal comprising particles can easily be detected by visual inspection at least if the diameter of the solid particles in which the metals are comprised is larger than the wavelength of visible light. Of course, methods such as quasi-elastic light scattering (QELS) or near forward scattering which are known to the skilled person can also be used to ensure that in no point in time of the process of the solid route, all metals are in the solute state.

The protic liquid to be applied in the solid or solution route of this invention for preparing catalyst can be any protic liquid. Examples include water, carboxylic acids, and alcohols such as methanol or ethanol. Preferably, a liquid comprising water such as mixtures of an alcohol and water and more preferably water is used as protic liquid in this solid route. Also different protic liquids can be applied simultaneously in the solid route. For instance, it is possible to add a suspension of a metal component in ethanol to an aqueous solution of another metal component. In some cases, a metal component can be used which dissolves in its own crystal water. The crystal water serves as protic liquid in this case.

The Group VIB metal generally comprises chromium, molybdenum, tungsten, or mixtures thereof. Suitable Group VIII non-noble metals are, e.g., iron, cobalt, nickel, or mixtures thereof. Preferably, a combination of metal components comprising nickel, molybdenum, and tungsten or nickel, cobalt, molybdenum, and tungsten is applied in the process of the solid route. If the protic liquid is water, suitable nickel components, which are at least partly in the solid state during contacting comprise water-insoluble nickel components such as nickel carbonate, nickel hydroxide, nickel phosphate, nickel phosphite, nickel formiate, nickel sulfide, nickel molybdate, nickel tungstate, nickel oxide, nickel alloys such as nickel-molybdenum alloys, Raney nickel, or mixtures thereof. Suitable molybdenum components, which are at least partly in the solid state during contacting, comprise water-insoluble molybdenum components such as molybdenum (di- and tri) oxide, molybdenum carbide, molybdenum nitride, aluminum molybdate, molybdic acid (e.g., H 2 MoO 4 ), molybdenum sulfide, or mixtures thereof. Finally, suitable tungsten components which are at least partly in the solid state during contacting comprise tungsten di- and trioxide, tungsten sulfide (WS 2 and WS 3 ), tungsten carbide, tungstic acid (e.g., H 2 WO 4 —H 2 O, H 2 W 4 O 13 —9H 2 O), tungsten nitride, aluminum tungstate (also meta-, or polytungstate) or mixtures thereof. These components are generally commercially available or can be prepared by, e.g., precipitation, e.g., nickel carbonate can be prepared from a nickel chloride, sulfate, or nitrate solution by adding an appropriate amount of sodium carbonate. It is generally known to the skilled person to choose the precipitation conditions in such a way as to obtain the desired morphology and texture.

In general, metal components, which mainly contain C, O, and/or H beside the metal, are preferred because they are less detrimental to the environment. Nickel carbonate is a preferred metal component to be added at least partly in the solid state because when nickel carbonate is applied, CO 2 evolves and positively influences the pH of the reaction mixture. Further, due to the transformation of carbonate into CO 2 , the carbonate does not end up in the wastewater.

Preferred nickel components which are added in the solute state are water-soluble nickel components (e.g., nickel nitrate, nickel sulfate, nickel acetate, nickel chloride, or mixtures thereof). Preferred molybdenum and tungsten components which are added in the solute state are water-soluble molybdenum and tungsten components, such as alkali metal or ammonium molybdate (also peroxo-, di-, tri-, tetra-, hepta-, octa-, or tetradecamolybdate), Mo—P heteropolyanion compounds, Wo—Si heteropolyanion compounds, W—P heteropolyanion compounds, W—Si heteropolyanion compounds, Ni—Mo—W heteropolyanion compounds, Co—Mo—W heteropolyanion compounds, alkali metal or ammonium tungstates (also meta-, para-, hexa-, or polytungstate), or mixtures thereof.

Preferred combinations of metal components are nickel carbonate, tungstic acid, and molybdenum oxide. Another preferred combination is nickel carbonate, ammonium dimolybdate, and ammonium metatungstate. It is within the scope of the skilled person to select further suitable combinations of metal components. It must be noted that nickel carbonate always comprises a certain amount of hydroxy groups. It is preferred that the amount of hydroxy groups present in the nickel carbonate be high.

An alternative method of preparing the catalysts used in the practice of the present invention is to prepare the bulk catalyst composition by a process comprising reacting in a reaction mixture a Group VIII non-noble metal component in solution and a Group VIB metal component in solution to obtain a precipitate. As in the case of the solid route, preferably, one Group VIII non-noble metal component is reacted with two Group VIB metal components. The molar ratio of Group VIB metals to Group VIII non-noble metals applied in the process of the solution route is preferably the same as described for the solid route. Suitable Group VIB and Group VIII non-noble metal components are, e.g., those water-soluble nickel, molybdenum and tungsten components described above for the solid route. Further Group VIII non-noble metal components are, e.g., cobalt or iron components. Further Group VIB metal components are, e.g. chromium components. The metal components can be added to the reaction mixture in solution, suspension or as such. If soluble salts are added as such, they will dissolve in the reaction mixture and subsequently be precipitated. Suitable Group VIB metal salts which are soluble in water are ammonium salts such as ammonium dimolybdate, ammonium tri-, tetra- hepta-, octa-, and tetradeca-molybdate, ammonium para-, meta-, hexa-, and polytungstate, alkali metal salts, silicic acid salts of Group VIB metals such as molybdic silicic acid, molybdic silicic tungstic acid, tungstic acid, metatungstic acid, pertungstic acid, heteropolyanion compounds of Mo—P, Mo—Si, W—P, and W—Si. It is also possible to add Group VIB metal-containing compounds which are not in solution at the time of addition, but where solution is effected in the reaction mixture. Examples of these compounds are metal compounds which contain so much crystal water that upon temperature increase they will dissolve in their own metal water. Further, non-soluble metal salts may be added in suspension and as such, the solution is effected in the reaction mixture. Suitable non-soluble metal salts are heteropolyanion compounds of Co—Mo—W (moderately soluble in cold water), heteropolyanion compounds of Ni—Mo—W (moderately soluble in cold water).

The reaction mixture is reacted to obtain a precipitate. Precipitation is effected by adding a Group VIII non-noble metal salt solution at a temperature and pH at which the Group VIII non-noble metal and the Group VIB metal precipitate, adding a compound which complexes the metals and releases the metals for precipitation upon temperature increase or pH change or adding a Group VIB metal salt solution at a temperature and pH at which the Group VIII non-noble metal and Group VIB metal precipitate, changing the temperature, changing the pH, or lowering the amount of the solvent. The precipitate obtained with this process appears to have high catalytic activity. In contrast to the conventional hydroprocessing catalysts, which usually comprise a carrier impregnated with Group VIII non-noble metals and Group VIB metals, said precipitate can be used without a support. Unsupported catalyst compositions are usually referred to as bulk catalysts. Changing the pH can be done by adding base or acid to the reaction mixture, or adding compounds, which decompose upon temperature, increase into hydroxide ions or H + ions that respectively increase or decrease the pH. Examples of compounds that decompose upon temperature increase and thereby increase or decrease the pH are urea, nitrites, ammonium cyanate, ammonium hydroxide, and ammonium carbonate.

In an illustrative process according to the solution route, solutions of ammonium salts of a Group VIB metal are made and a solution of a Group VIII non-noble metal nitrate is made. Both solutions are heated to a temperature of approximately 90° C. Ammonium hydroxide is added to the Group VIB metal solution. The Group VIII non-noble metal solution is added to the Group VIB metal solution and direct precipitation of the Group VIB and Group VIII non-noble metal components occurs. This process can also be conducted at lower temperature and/or decreased pressure or higher temperature and/or increased pressure.

In another illustrative process according to the solution route, a Group VIB metal salt, a Group VIII metal salt, and ammonium hydroxide are mixed in solution together and heated so that ammonia is driven off and the pH is lowered to a pH at which precipitation occurs. For instance, when nickel, molybdenum, and tungsten components are applied, precipitation typically occurs at a pH below 7.

Independently from whether the solid or solution route is chosen in step (i), the resulting bulk catalyst composition preferably comprises and more preferably consists essentially of bulk catalyst particles having the characteristics of the bulk catalyst particles described under the heading “Catalyst compositions of the invention.”

The bulk catalyst composition can generally be directly shaped into hydroprocessing particles. If the amount of liquid of the bulk catalyst composition is so high that it cannot be directly subjected to a shaping step, a solid liquid separation can be performned before shaping. Optionally, the bulk catalyst composition, either as such or after solid liquid separation, can be calcined before shaping.

The median diameter of the bulk catalyst particles is at least 50 nm, more preferably at least 100 nm, and preferably not more than 5000 μn and more preferably not more than 3000 μm. Even more preferably, the median particle diameter lies in the range of 0.1-50 m and most preferably in the range of 0.5-50 μμm.

If a binder material is used in the preparation of the catalyst composition it can be any material that is conventionally applied as a binder in hydroprocessing catalysts. Examples include silica, silica-alumina, such as conventional silica-alumina, silica-coated alumina and alumina-coated silica, alumina such as (pseudo)boehmite, or gibbsite, titania, zirconia, cationic clays or anionic clays such as saponite, bentonite, kaoline, sepiolite or hydrotalcite, or mixtures thereof. Preferred binders are silica, silica-alumina, alumina, titanic, zirconia, or mixtures thereof. These binders may be applied as such or after peptization. It is also possible to apply precursors of these binders that, during the process of the invention are converted into any of the above-described binders. Suitable precursors are, e g., alkali metal aluminates (to obtain an alumina binder), water glass (to obtain a silica binder), a mixture of alkali metal aluminates and water glass (to obtain a silica alumina binder), a mixture of sources of a di-, tri-, and/or tetravalent metal such as a mixture of water-soluble salts of magnesium, aluminum and/or silicon (to prepare a cationic clay and/or anionic clay), chlorohydrol, aluminum sulfate, or mixtures thereof.

If desired, the binder material may be composited with a Group VIB metal and/or a Group VIII non-noble metal, prior to being composited with the bulk catalyst composition and/or prior to being added during the preparation thereof. Compositing the binder material with any of these metals may be carried out by impregnation of the solid binder with these materials. The person skilled in the art knows suitable impregnation techniques. If the binder is peptized, it is also possible to carry out the peptization in the presence of Group VIB and/or Group VIII non-noble metal components.

If alumina is applied as a binder, the surface area preferably lies in the range of 100-400 m 2 /g, and more preferably 150-350 m 2 /g, measured by the B.E.T. method. The pore volume of the alumina is preferably in the range of 0.5-1.5 ml/g measured by nitrogen adsorption.

Generally, the binder material to be added in the process of the invention has less catalytic activity than the bulk catalyst composition or no catalytic activity at all. Consequently, by adding a binder material, the activity of the bulk catalyst composition may be reduced. Therefore, the amount of binder material to be added in the process of the invention generally depends on the desired activity of the final catalyst composition. Binder amounts from 0-95 wt. % of the total composition can be suitable, depending on the envisaged catalytic application. However, to take advantage of the resulting unusual high activity of the composition of the present invention, binder amounts to be added are generally in the range of 0.5-75 wt. % of the total composition.

The catalyst composition can be directly shaped. Shaping comprises extrusion, pelletizing, beading, and/or spray drying. It must be noted that if the catalyst composition is to be applied in slurry type reactors, fluidized beds, moving beds, expanded beds, or ebullating beds, spray drying or beading is generally applied for fixed bed applications, generally, the catalyst composition is extruded, pelletized and/or beaded. In the latter case, prior to or during the shaping step, any additives that are conventionally used to facilitate shaping can be added. These additives may comprise aluminum stearate, surfactants, graphite, or mixtures thereof. These additives can be added at any stage prior to the shaping step. Further, when alumina is used as a binder, it may be desirable to add acids prior to the shaping step such as nitric acid to increase the mechanical strength of the extrudates.

It is preferred that a binder material is added prior to the shaping step. Further, it is preferred that the shaping step is carried out in the presence of a liquid, such as water. Preferably, the amount of liquid in the extrusion mixture, expressed as LOI is in the range of 20-80%.

The resulting shaped catalyst composition can, after an optional drying step, be optionally calcined. Calcination, however, is not essential to the process of the invention. If a calcination is carried out in the process of the invention, it can be done at a temperature of, e.g., from 100°-600° C. and preferably 350° C. to 500° C. for a time varying from 0.5 to 48 hours. The drying of the shaped particles is generally carried out at temperatures above 100° C.

In a preferred embodiment of the invention, the catalyst composition is subjected to spray drying, (flash) drying, milling, kneading, or combinations thereof prior to shaping. These additional process steps can be conducted either before or after a binder is added, after solid-liquid separation, before or after calcination and subsequent to re-wetting. It is believed that by applying any of the above-described techniques of spray drying, (flash) drying, milling, kneading, or combinations thereof, the degree of mixing between the bulk catalyst composition and the binder material is improved. This applies to both cases where the binder material is added before or after the application of any of the above-described methods. However, it is generally preferred to add the binder material prior to spray drying and/or any alternative technique. If the binder is added subsequent to spray drying and/or any alternative technique, the resulting composition is preferably thoroughly mixed by any conventional technique prior to shaping. An advantage of, e.g., spray drying is that no wastewater streams are obtained when this technique is applied.

Furthermore, a cracking component may be added during catalyst preparation. The cracking component may serve as an isomerization enhancer. The cracking component can be any conventional cracking component such as cationic clays, anionic clays, zeolites such as ZSM-5, (ultra-stable) zeolite Y, zeolite X, ALPO's, SAPO's, amorphous cracking components such as silica-alumina, or mixtures thereof. It will be clear that some materials may act as a binder and a cracking component at the same time. For instance, silica-alumina may have at the same time a cracking and a binding finction.

If desired, the cracking component may be composited with a Group VIB metal and/or a Group VIII non-noble metal prior to being composited with the bulk catalyst composition and/or prior to being added during the preparation thereof. Compositing the cracking component with any of these metals may be carried out by impregnation of the cracking component with these materials.

The cracking component, which can comprise about 0-80 wt. %, based on the total weight of the catalyst, can be added at any stage of the process of the present invention prior to the shaping step. However, it is preferred to add the cracking component during the compositing step (ii) with the binder.

Generally, which of the above-described cracking components is added, depends on the envisioned catalytic application of the final catalyst composition. A zeolite is preferably added if the resulting composition shall be applied in hydrocracking or fluid catalytic cracking. Other cracking components such as silica-alumina or cationic clays are preferably added if the final catalyst composition shall be used in hydrotreating applications. The amount of cracking material that is added depends on the desired activity of the final composition and the application envisaged and thus may vary from 0-80 wt. %, based on the total weight of the catalyst composition.

If desired, firther materials can be added in addition to the metal components already added. These materials include any material that is added during conventional hydroprocessing catalyst preparation. Suitable examples are phosphorus compounds, borium compounds, fluor-containing compounds, additional transition metals, rare earth metals, fillers, or mixtures thereof.

Suitable phosphorus compounds include ammonium phosphate, phosphoric acid, or organic phosphorus compounds. Phosphorus compounds can be added at any stage of the process of the present invention prior to the shaping step and/or subsequent to the shaping step. If the binder material is peptized, phosphorus compounds can also be used for peptization. For instance, the binder can be peptized by contacting the binder with phosphoric acid or with a mixture of phosphoric and nitric acid.

Suitable additional transition metals are, e.g., rhenium, ruthenium, rhodium, iridium, chromium, vanadium, iron, cobalt, platinum, palladium, cobalt, nickel, molybdenum, or tungsten. Nickel, molybdenum, and tungsten can be applied in the form of any of the water-insoluble nickel, molybdenum and/or tungsten components that are described above for the solid route. These metals can be added at any stage of the process of the present invention prior to the shaping step. Apart from adding these metals during the process of the invention, it is also possible to composite the final catalyst composition therewith. It is, e.g., possible to impregnate the final catalyst composition with an impregnation solution comprising any of these metals.

The processes of the present invention for preparing the bulk catalyst compositions may further comprise a sulfidation step. Sulfidation is generally carried out by contacting the catalyst composition or precursors thereof with a sulfur-containing compound such as elementary sulfur, hydrogen sulfide, or polysulfides. The sulfidation can generally be carried out subsequently to the preparation of the bulk catalyst composition but prior to the addition of a binder material, and/or subsequently to the addition of the binder material but prior to subjecting the catalyst composition to spray drying and/or any alternative method, and/or subsequently to subjecting the composition to spray drying and/or any alternative method but prior to shaping, and/or subsequently to shaping the catalyst composition. It is preferred that the sulfidation is not carried out prior to any process step that reverts the obtained metal sulfides into their oxides. Such process steps are, e.g., calcination or spray drying or any other high temperature treatment in the presence of oxygen. Consequently, if the catalyst composition is subjected to spray drying and/or any alternative technique, the sulfidation should be carried out subsequent to the application of any of these methods.

Additionally to, or instead of, a sulfidation step, the bulk catalyst composition may be prepared from at least one metal sulfide. If, e.g., the solid route is applied in step (i), the bulk catalyst component can be prepared form nickel sulfide and/or molybdenum sulfide and/or tungsten sulfide.

If the catalyst composition is used in a fixed bed process, the sulfidation is preferably carried out subsequent to the shaping step and, if applied, subsequent to the last calcination step. Preferably, the sulfidation is carried out ex situ, i.e., the sulfidation is carried out in a separate reactor prior to loading the sulfided catalyst composition into the hydroprocessing unit. Furthermore, it is preferred that the catalyst composition is both sulfided ex situ and in situ.

One or more of the reaction zones of any or both of the hydrodesulfurization stages, may contain a conventional hydrodesulfurization catalyst. Suitable conventional hydrodesulfurization catalysts for use in the present invention includes those that are comprised of at least one Group VIII metal, preferably Fe, Co, or Ni, more preferably Co and/or Ni, and most preferably Co; and at least one Group VI metal, preferably Mo or W, more preferably Mo, on a relatively high surface area support material, preferably alumina. Other suitable hydrodesulfurization catalyst supports include zeolites, amorphous silica-alumina, and titania-alumina. Noble metal catalysts can also be employed, preferably when the noble metal is selected from Pd and Pt. It is within the scope of the present invention that more than one type of hydrodesulfurization catalyst be used in the same reaction vessel. The Group VIII metal is typically present in an amount ranging from about 2 to 20 wt. %, preferably from about 4 to 12 wt. %. The Group VI metal will typically be present in an amount ranging from about 5 to 50 wt. %, preferably from about 10 to 40 wt. %, and more preferably from about 20 to 30 wt. %. All metal weight percents are on support. By “on support” we mean that the percents are based on the weight of the support. For example, if the support were to weigh 100 g., then 20 wt. % Group VIII metal would mean that 20 g. of Group VIII metal was on the support.

It has been found that in this case, the bulk catalyst particles are sinter-resistant. Thus, the active surface area of the bulk catalyst particles is maintained during use. The molar ratio of Group VIB to Group VIII non-noble metals ranges generally from 10:1-1:10 and preferably from 3:1-1:3. In the case of a core-shell structured particle, these ratios of course apply to the metals contained in the shell. If more than one Group VIB metal is contained in the bulk catalyst particles, the ratio of the different Group VIB metals is generally not critical. The same holds when more than one Group VIII non-noble metal is applied. In the case where molybdenum and tungsten are present as Group VIB metals, the molybenum:tungsten ratio preferably lies in the range of 9:1-1:9. Preferably, the Group VIII non-noble metal comprises nickel and/or cobalt. It is further preferred that the Group VIB metal comprises a combination of molybdenum and tungsten. Preferably, combinations of nickel/molybdenum/tungsten and cobalt/molybdenum/tungsten and nickel/cobalt/molybdenum/tungsten are used. These types of precipitates appear to be sinter-resistant. Thus, the active surface area of the precipitate is remained during use. The metals are preferably present as oxidic compounds of the corresponding metals, or if the catalyst composition has been sulfided, sulfidic compounds of the corresponding metals.

Preferably, the particles have a surface area of at least 50 m 2 /g, and more preferably of at least 100 m 2 /g measured via the BET method. It is furthermore preferred that the particles comprise 50-100 wt. %, and even more preferably 70-100 wt. % of at least one Group VIII non-noble metal and at least one Group VIB metal, based on the total weight of the particles, calculated as metal oxides. The amount of Group VIB and Group VIII non-noble metals can easily be determined via TEM-EDX.

It is desired that the pore size distribution of the particles is approximately the same as the one of conventional hydrotreating catalysts. More, in particular, these particles have preferably a pore volume of 0.05-5 ml/g, more preferably of 0.1-4 ml/g, still more preferably of 0.1-3 ml/g and most preferably 0.1-2 ml/g determined by nitrogen adsorption. Preferably, pores smaller than 1 nm are not present. Furthermore, these particles preferably have a median diameter of at least 50 nm, more preferably of at least 100 nm, and preferably not more than 5000 μm, and more preferably not more than 3000 μn. Even more preferably, the median particle diameter lies in the range of 0.1-50 μm, and most preferably in the range of 0.5-50 μm.

The surface area of the catalyst composition preferably is at least 40 m 2 /g, more preferably at least 80 m 2 /g and most preferably at least 120 m 2 /g. The total pore volume of the catalyst composition is preferably at least 0.05 ml/g and more preferably at least 01 ml/g as determined by water porosimetry. To obtain catalyst compositions with high mechanical strength, it may be desirable that the catalyst composition of the invention has a low macroporosity.

It was found that the bulk catalyst particles have a characteristic X-ray diffraction pattern which differs from catalysts obtained by co-mixing and conventional hydroprocessing catalysts obtained by impregnation. The X-ray diffraction pattern of the bulk catalyst particles comprises, and preferably essentially consists of, peaks characteristic to the reacted metal components. If, e.g., nickel hydroxy-carbonate has been contacted with a molybdenum and tungsten component as described above, the resulting bulk catalyst particles are characterized by an X-ray diffraction pattern which comprises peaks at d values of (4.09), 2.83, 2.54, 2.32, 2.23, 1.71, (1.54), 1.47. Values in brackets indicate that the corresponding peaks are rather broad and/or have a low intensity or are not distinguished at all. The term “the X-ray diffraction pattern essentially consists of” these peaks means that apart from these peaks, there are essentially no further peaks contained in the diffraction pattern. The precipitate for catalyst obtained by the solution route has a characteristic X-ray diffraction pattern which differs from catalyst obtained by co-mixing and conventional hydroprocessing catalysts obtained by impregnation. For instance the X-ray diffraction pattern of a Ni—Mo—W precipitate as prepared by the solution route has peaks at d values of 2.52, 1.72 and 1.46.

Also as previously stated, the catalyst composition may comprise conventional hydroprocessing catalysts. The binder materials and cracking components of the conventional hydroprocessing catalyst generally comprise any of the above-described binder materials and cracking components. The hydrogenation metals of the conventional hydroprocessing catalyst generally comprise Group VIB and Group VIII non-noble metals such as combinations of nickel or cobalt with molybdenum or tungsten. Suitable conventional hydroprocessing catalysts are, e.g., hydrotreating catalysts. These catalysts can be in the spent, regenerated, or fresh state.

As will be clear from the above, it is possible to add the Group VIII non-noble metal-containing compound and the Group VIB metal-containing compound in various ways, at various temperatures and pHs, in solution, in suspension, and, as such, simultaneously and sequentially.

The precursor compound can also be readily prepared by one of several methods, including a variation of the boiling decomposition method used by Teichner and Astier in which a tungsten compound is added to the initial mixture of a molybdenum salt, a nickel salt, and ammonium hydroxide. Direct precipitation and pH controlled precipitation may also be used to prepare the precursor compound. In all cases, however, water soluble salts of nickel, molybdenum, and tungsten are employed.

Preferably, the molybdenum and tungsten salts are ammonium compounds, e.g., ammonium molybdate, ammonium metatungstate, while the nickel salt may be the nitrate or hydrated nitrates.

The decomposed precursor can be sulfided or pre-sulfided by a variety of known methods. For example, the decomposition product can be contacted with a gas comprising H 2 S and hydrogen, e.g., 10% H 2 S/H 2 , at elevated temperatures for a period of time sufficient to sulfide the decomposition product, usually at the point of H 2 S breakthrough in the exit gas. Sulfiding can also be effected, in situ, by passing a typical feedstock containing sulfur over the decomposition product.

The present invention also provides a bulk multimetallic catalyst comprised of at least one Group VIII nonnoble metal and at least one Group VIB metal. Preferable, the ratio of Group VIB to Group VIII metals is from about 10:1 to about 1:10. In a perferred embodiment, the Group VIII non-nobel metal is selected from Ni and Co and the Group VIB metal is selected from Mo and W. The methods of catalyst formulation and preparation described herein, are also applicable to the above-described catalyst. Additionally, this catalyst can be used as a hydrotreating and/or hydrofinishing catalyst in the oxo process.

Process conditions applicable for the use of the catalysts described herein may vary widely depending on the feedstock to be treated. Thus, as the boiling point of the feed increases, the severity of the conditions will also increase. The following table serves to illustrate typical conditions for a range of feeds.

	TYPICAL BOILING			SPACE VELOCITY
FEED	RANGE ° C.	TEMP. ° C.	PRESS, BAR	V/V/HR	H 2 GAS RATE SCF/B
naphtha	25-210	100-370	10-60	0.5-10	100-2,000
diesel	170-350	200-400	15-110	0.5-4	500-6,000
heavy gas oil	325-475	260-430	15-170	0.3-2	1000-6,000
lube oil	290-550	200-450	6-210	0.2-5	100-10,000
residuum	10-50% >575	340-450	65-1100	0.1-1	2,000-10,000

The following examples will serve to illustrate, but not limit, this invention.

EXAMPLE 1

Preparation of NH 4 —Ni—Mo—O Phase (boiling decomposition as per Teichner and Astier procedure)

In a 1 liter flask, 26.5 g ammonium molybdate (0.15 moles Mo) and 43.6 g nickel nitrate hexahydrate (0.15 moles Ni) were dissolved in 300 cc of water so that the resulting pH equaled 4.3. To this solution, a concentrated NH 4 OH solution was added. At first, a precipitate formed which on further addition of NH 4 OH dissolved to give a clear blue solution with a pH of 8.3, and additional NH 4 OH (˜250 cc) was added until a pH of 10 was reached. The solution was heated to 90° C. for 3 h during which ammonia gas evolved and a green precipitate formed. The final pH lay between 6.8 and 7. The suspension was cooled to room temperature, filtered, washed with water and dried at 120° C. overnight. About 18.6 g of material was obtained. The sample analyzed for Ni at 26.6 wt. % and Mo at 34 wt. %. The X-ray diffraction spectra of the phase matches the pattern reported by Teichner.

EXAMPLE 2

Preparation of NH 4 —Ni—Mo 0.5 W 0.5 O by Boiling Decomposition

In a 1 liter flask, 13.2 g ammonium molybdate (0.075 moles Mo), 18.7 g ammonium metatungstate (0.075 moles W) and 43.6 g nickel nitrate hexahydrate (0.15 moles Ni) were dissolved in 300 cc of water so that the resulting pH equaled 4.3. To this solution, a concentrated NH 4 OH solution (˜600 cc) was added until the pH reached 10. At this point, some precipitate remained. The solution was refluxed at ˜100° C. for 3 h. During this heating, the precipitate dissolved to give a clear blue solution and on further heating, a green precipitate formed. The heating was continued until the pH reached between 6.8 and 7. The suspension was cooled to room temperature, filtered, washed with water and dried at 120° C. overnight. 18 grams of material is obtained. The X-ray diffraction spectra of the phase is given in FIG. 2 showing an amorphous background with the two largest peaks at d=2.58 and 1.70 Å.

EXAMPLE 3

Preparation of NH 4 —Ni—Mo 0.5 W 0.5 —O by Direct Precipitation

In a 1 liter flask, 17.65 g of ammonium molybdate (0.1 mole Mo) and 24.60 g of ammonium metatungstate (0.1 mole W) were dissolved in 800 cc of water giving a solution pH of ˜5.2. To this solution 0.4 moles of NH 4 OH (˜30 cc) was added, raising the pH to ˜9.8 (solution A). This solution was warmed to 90° C. A second solution was prepared by adding 58.2 g of nickel nitrate, (0.2 moles Ni) which was dissolved in 50 cc of water (solution B) and maintained at 90° C. This solution was added dropwise at a rate of 7 cc/min into the ammonium molybdate/ammonium metatungstate solution. A precipitate begins to form after ¼ of the solution was added. This suspension, which was at a pH −6.5, was stirred for 30 minutes while the temperature was maintained at 90° C. The material was filtered hot, washed with hot water, and dried at 120° C. Approximately 38 g of material was recovered.

EXAMPLE 4

Preparation of NH 4 —Ni—Mo 0.5 —Mo 0.5 W 0.5 -O by Controlled pH Precipitation

Two solutions were prepared with the same amounts of nickel, tungsten, molybdenum and ammonium hydroxide as are described in Example 3 (solutions A and B) except that each solution contained about 700 cc of water. The two solutions were added into a separate vessel initially containing 400 cc of water held at 90° C. Solution B (the acidic solution) was pumped into the vessel at a constant rate of ˜15 cc/min, while solution A is added through a separate pump which is under feedback PC control and set to maintain the pH at 6.5. On mixing the two solutions, a precipitate forms. The slurry was stirred at 90° C. for 30 minutes, filtered hot, washed with hot water, and dried at 120° C.

EXAMPLE 5

Catalytic Evaluation Using Dibenzothiophene (DBT)

1.5-2 g of the catalysts of Examples 1-4 were placed in a quartz boat which was in turn inserted into a horizontal quartz tube and placed into a Lindberg furnace. The temperature was raised to 370° C. in about one hour with N 2 flowing at 50 cc/m, and the flow continued for 1.5 h at 370° C. N 2 was switched off and 10% H 2 S/H 2 was then added to the reactor at 20 cc/m, the temperature increased to 400° C., and held there for 2 hours. The heat was then shut off and the catalyst cooled in flowing H 2 S/H 2 to 70° C., at which point this flow was discontinued and N 2 was added. At room temperature, the quartz tube was removed and the material transferred into a N 2 purged glove box. Catalysts were evaluated in a 300 cc modified Carberry batch reactor designed for constant hydrogen flow. The catalyst was pilled and sized to 20/40 mesh and one gram was loaded into a stainless steel basket, sandwiched between a layer of mullite beads. 100 cc of liquid feed, containing 5 wt. % dibenzothiophene in decalin was added to the autoclave. A hydrogen flow of 100 cc/min was passed through the reactor and the pressure was maintained at 3150 kPa using a back pressure regulator. The temperature was raised to 350° C. at 5-6 deg/min and run until either 50% DBT was converted or until 7 hours was reached. A small aliquot of product was removed every 30 minutes and analyzed by GC. Rate constants for the overall conversion as well as the conversion to the reaction products biphenyl (BP) and cyclohexylbenzene (CHB) were calculated as described by M. Daage and R. R. Chianelli [J. Cat. 149, 414-27 (1994)] and are shown in Table 1. As described in that article, high selectivities to cyclohexylbenzene relative to BP during the desulfurization reaction are a good indication of a catalyst with high hydrodenitrogenation activity, whereas high selectivities of BP relative to CHB indicates a catalyst with high hydrodesulfurization activity.

The results show that partial substitution of tungsten for molybdenum results in catalysts that are substantially higher for DBT conversion. A standard supported Ni—Mo on A 1 2 O 3 catalyst is also shown for comparison. The high CHB/BP ratio suggests that the catalysts are active for HDN.

TABLE 1
Comparison of Activity in DBT Conversion Tests With
Tungsten Addition by Different Preparation Schemes
			K Total	CHB/BP
	Preparation		@	@
Catalyst	Technique	Example #	350° C.	350° C.
NH 4 -Ni-Mo-O	boiling	1	106	10.4
	decomposition
NH 4 -Ni-Mo .5 W .5 -O	boiling	2	171	10.2
	decomposition
NH 4 -Ni-Mo .5 W .5 -O	direct	3	167	12.4
	precipitation
NH 4 -Ni-Mo .5 W .5 -O	controlled pH	4	181	12.0
	preparation
Ni,Mo/Al 2 O 3	impregnation		129	6.4

EXAMPLE 6

A series of catalysts were prepared in accordance with the general preparation scheme of Example 2 (i.e., boiling decomposition) but varying the Mo and W relative ratios by changing the amount of ammonium molybdate and ammonium metatungstate added to the solutions. Decomposition was effected as described in Example 5. The catalysts so prepared are shown in Table 2, along with their catalytic activities for DBT measured as described in Example 5.

TABLE 2
Comparison of Activity in DBT Conversion Tests
With Variation in Relative W and Mo Content
				Nickel
		Ammonium	Ammonium	nitrate
		molybdate	metatungstate	hexahydrate	K total @	CHB/BP @
Catalyst	Sample	(g)	(g)	(g)	350° C.	350° C.
NH 4 —NiW—O	18983-97	0	36.95	43.62	128	11.3
NH 4 —NiMo .1 W .9 —O	18983-125	2.65	33.62	43.62	132	14.1
NH 4 —NiMo .3 W .7 —O	18983-101	7.94	25.87	43.62	154	11.6
NH 4 —NiMo .5 W .5 —O	18357-109	13.17	18.74	43.62	171	10.2
NH 4 —NiMo .7 W .3 —O	18983-95	18.54	11.09	43.62	158	11.5
NH 4 —NiMo .9 W .1 —O	18983-92	23.83	3.69	43.62	141	10.5

The data shows that the most active catalyst contains an approximately equimolar mixture of tungsten and molybdenum.

EXAMPLE 7

A series of catalysts were prepared as described in Example 3 (direct precipitation) in which equimolar mixtures of Mo and W were precipitated, but the nickel content was varied. Decomposition was effected as described in Example 5. The catalysts so prepared are shown in Table 3, along with their catalytic activities for DBT measured as described in Example 5.

TABLE 3
Variation of Nickel Content in NH 4 —Ni—Mo .5 W .5 —O Catalysts
				Nickel
		Ammonium	Ammonium	nitrate	K Total	CHB/BP
		molybdate	metatungstate	hexahydrate	@	@
Catalyst	Sample	(g)	(g)	(g)	350° C.	350° C.
NH 4 —Ni 0.75 Mo .5 W .5 —O	19086-110	17.65	24.6	43.65	171	13.0
NH 4 —Ni 1.0 Mo .5 W .5 —O	19086-82	17.65	24.6	58.2	167	12.4
NH 4 —Ni 1.25 Mo .5 W .5 —O	19086-111	17.65	24.6	72.75	174	11.0
NH 4 —Ni 1.5 Mo .5 W .5 —O	19086-112	17.65	24.6	87.3	148	9.55

Catalytic performance does not change substantially with variations in Ni from 0.75 to 1.5, although K appears to go through a maximum at about 1.25 Ni.

EXAMPLE 8

A series of catalysts were prepared in which the quantity of NH 4 OH used in the preparation was varied. The catalysts were prepared in accordance to the procedure described in Example 3 except that the amount of NH 4 OH in solution A was varied to change to NH 4 OH/Ni molar ratio when the two solutions were mixed. Decomposition was effected as described in Example 5. The catalysts so prepared are shown in Table 4 along with their catalytic activities for DBT measured as described in Example 5.

TABLE 4
Variation in NH 4 OH Addition to Preparation
				Nickel
Catalyst		Ammonium	Ammonium	nitrate	cm 3	K Total	K CHB/
NH 4 OH/Ni		molybdate	metatungstate	hexahydrate	conc	@	BP @
mole ratio	Sample	(g)	(g)	(g)	NH 4 OH	350° C.	350° C.
1:2	19086-96	17.65	24.6	43.65	6.8	102	10.5
1:1	19086-97	17.65	24.6	58.2	14	137	10.4
2:1	19086-82	17.65	24.6	72.75	30	167	12.4
3:1	19086-104	17.65	24.6	87.3	41	164	11.4
4:1	19086-106	17.65	24.6	87.3	55	161	12.1

While decomposition of the precursor compound will drive off most, if not all, of the ammonium portion of the precursor, the preparation of the precursor and the catalytic utility of the decomposition product can be affected by the amount of NH 4 OH employed. Thus, the effectiveness of the decomposition product as a catalyst is enhanced when the NH 4 OH/Ni ratio in the preparation of the precursor compound is from about 1:1 to about 4:1, preferably about 1.5:1 to about 4:1, and more preferably about 2:1 to about 4:1. While not wishing to be bound by any particular theory or mechanism, there is some evidence the NH 4 OH/Ni ratio causes the Ni—M—W—O phase to change in the decomposition product.

EXAMPLE 9

The catalysts of Examples 1 and 2 were compared against standard supported Ni—Mo catalysts for the conversion of a LSADO (low sulfur auto diesel oil feed). This feed contained 510 wppm sulfur, 50 wppm nitrogen, and 30.6% aromatics with a gravity of 39.8° API. The catalysts were tested at 579° F., 650 psig of H 2 , and 1850 SCFB/B of H 2 . The relative activities of the different catalysts are summarized in Table 5.

TABLE 5
Relative Hydrotreating Activities on LSADO Feed
		Relative	Relative
		Volumetric HDS	Volumetric HDN
	Catalyst	Activity	Activity
	Ni,Mo/Al 2 O 3	1	1
	NH 4 -NiMo-O	0.25	0.50
	NH 4 -Ni 1.0 Mo .5 W .5 -O	1.4	2.05

The Ni, Mo/Al 2 O 3 catalyst is a standard HDN/HDS catalyst, the NH 4 —Ni—Mo phase is the bulk phase with no tungsten, and the NH 4 —Ni 1.0 Mo 0.5 W 0.5 —O is the bulk phase with partial substitution of W for Mo. The NH 4 —NiMo—O catalyst is also representative of known compounds. The catalyst of this invention is illustrated by NH 4 —Ni 1.0 Mo 0.5 W 0.5 —O and the data show the clear advantage of ammonium nickel tungsten molybdate for HDN activity.

EXAMPLE 10

Preparation of a Bulk Catalyst Composition According to the Solid Route

18.1 kg-ammonium dimolybdate (15.33 kg MoO 3 ) are dissolved in 575 liters water. Subsequently 28.5 kg ammonium metatungstate (24 69 kg WO 3 ) is added to the solution. The resulting solution is preheated up to 90° C. 26.5 kg NiCO 3 (49.7% Ni) powder is mixed with water and the resulting paste is added to the ammonium dimolybdate/ammonium metatungstate solution. The resulting mixture is reacted for 7 hours at 89° C.

EXAMPLE 11

Preparation of a Bulk Catalyst Composition According to the Solution Route

In a 1-liter flask, 13.2 g ammonium molybdate (0.075 moles Mo), 18.7 g ammonium metatungstate (0.075 moles W), and 43.6 g nickel nitrate hexahydrate (0.15 moles Ni) were dissolved in 300 ml water so that the resulting pH equaled 4.3. To this solution, a concentrated NH 4 OH solution (about 600 ml) was added until the pH reached 10. At this point, some precipitate remained. The solution was refluxed at 100° C. for 3 hours. During this heating, the precipitate dissolved to give a clear blue solution and on further heating, a green precipitate formed. The heating was continued until the pH reached a value between 6.8 and 7.0. The suspension was cooled to room temperature, filtered, washed with water and dried at 120° C. overnight. 18 grams of material were obtained.

EXAMPLE 12 (sample 2110587)

657 g of a NiMo—W bulk catalyst composition obtained according to the procedure described in Examples 10 or 11 was added to 1362 g of an aqueous slurry containing 125 g of alumina (prepared by precipitation of sodium aluminate and aluminum sulfate). The resulting Ni—Mo—W bulk catalyst—alumina composition was subsequently mixed at 80° C. until an LOI of 31% was obtained. The resulting composition was subsequently extruded and the extrudates were dried at 120° C. for about 90 minutes and subsequently calcined at 385° C. for one hour in air.

EXAMPLE 13 (sample 2110598)

The process of Example 12 was repeated except that instead of the alumina suspension, a silica sol containing 10 wt. % silica was applied.

EXAMPLE 14 (sample 2110591)

657 g of a Ni—Mo—W bulk catalyst composition obtained according to the procedure described in Examples 7 or 8 was added to 510 g of a boehmite paste containing 125 g boehmite. The rebuffing paste was mixed at 60° C. to obtain an LOI of 42%. The resulting composition was extruded, dried and calcined as described in Example 12.

EXAMPLE 15 (sample 2110469)

The procedure described in Example 7 or 8 was repeated except that alumina is present during the preparation of the bulk catalyst composition. To 755 g of the resulting dried Ni—Mo—W bulk catalyst-alumina composition containing 60 g alumina, 461 g water, and a small amount of nitric acid were added. The resulting mixture was mixed at 70° C. while evaporating water until an LOI of 34% was obtained. The resulting composition was extruded, dried and calcined as described in Example 12.

EXAMPLE 16

Ammonium molybdate, ammonium tungsten and/or ammonium chromate are dissolved and combined in a first reactor. The temperature is increased to 90° C. The Group VIII salt is dissolved in a second reactor and heated to 90° C. Ammonium hydroxide is added to the first reactor to form a basic solution. The Group VIII metal solution is added to the first dropwise with stirring in 20 minutes. After 30 minutes, the precipitate is filtered and washed. The precipitate is dried overnight at 120° C. and calcined at 385° C.

EXAMPLE 17

The precipitation method of Example 16 was used to prepare a precipitate from ammonium dimolybdate, ammonium meta tungstate and Fe(III(NO3)3.9H2O in 98% yield comprising 41.2 wt. % Fe2O3, 21.3 wt. % MoO3, and 36.9 wt. % WO3. The surface area of the precipitate was 76 m2/g. The pore volume as measured up to 60 nm by the BET method using the adsorption curve was 0.147 ml/g.

EXAMPLE 18

The precipitation method of Example 16 was used to prepare a precipitate from Ni(CO 3 ) 2 .6H 2 O, (NH 4 ) 6 MO 7 O 24 .4H 2 O, and (NH 4 ) 2 Cr 2 O 7 in 87.7% yield comprising 52.2 wt. % NiO, 29.4 wt. % MoO 3 , and 16.6 wt. % Cr 2 O 3 . The surface area of the precipitate was 199 m 2 /g. The pore volume as measured up to 60 nm by the BET method using the adsorption curve was 0.276 ml/g.

EXAMPLE 19

The precipitation method of Example 16 was used to prepare a precipitate from Ni(CO 3 ) 2 .6H 2 O, (NH 4 ) 6 H 2 W 12 O 40 , and (NH 4 ) 2 Cr 2 O 7 in 87.7% yield comprising 44.0 wt. % NiO, 42.4 wt. % WO 3 , and 11.8 wt. % Cr 2 O 3 . The surface area of the precipitate was 199 m 2 /g. The pore volume as measured up to 60 nm by the BET method using the adsorption curve was 0.245 ml/g.

Claims

1. In a process for preparing Oxo alcohols by the catalyzed hydroformylation of olefins which comprises the steps of:(a) hydroformylating a hydrocarbon stream comprising at least one olefin selected from C4, C5, C6, C7, C8, C9, C10, C11, and C12 olefins by reaction of said olefin with carbon monoxide and hydrogen in the presence of a hydroformylation catalyst to produce a crude reaction product which contains carbonyl-containing compounds; (b) hydrogenating said crude reaction product of step (a) to reduce at least a portion of said carbonyl-containing compounds to alcohols; the improvement which comprises conducting step (b) in the presence of a bulk multimetallic catalyst comprised of at least one Group VIII non-noble metal and at least two Group VIB metals, wherein the ratio of Group VIB to Group VIII metals is from about 10:1 to about 1:10.

2. The process of claim 1, wherein said hydroformylation catalyst is selected from rhodium-containing catalysts and cobalt-containing catalyst.

3. The process of claim 2, wherein said hydroformylation catalyst is a cobalt carbonyl catalyst.

4. The process of claim 3, wherein said bulk multimetallic catalyst is a trimetallic catalyst comprised of two Group VIB metals and one Group VIII non-noble metal selected from Ni and Co.

5. The process of claim 4, wherein said Group VIB metals are Mo and W.

6. The process of claim 5, wherein the ratio of Mo to W is about 9:1 to about 1:9.

7. The process of claim 1, wherein said bulk multimetallic catalyst is represented by the formula:(X)b(Mo)c(W)dOz wherein X is a Group VIII non-noble metal, and the molar ratio of b: (c+d) is 0.5/1 to 3/1.

8. The process of claim 7, wherein the ratio of b:(c+d) is 0.75/1 to 1.5/1.

9. The process of claim 1, wherein said bulk multimetallic catalyst is essentially an amorphous material having a unique X-ray diffraction pattern showing crystalline peaks at d=2.53 Angstroms and d=1.70 Angstroms.

10. The process of claim 3, further comprising:(c) separating the product of step (b) and recovery therefrom Oxo alcohols containing a reduced amount of said carbonyl-containing compounds; and (d) hydrofmishing (by hydrogenation) the product of step (c) to provide a substantially pure alcohol product.

11. The process of claim 10, further comprising:(e) demetalling the crude reaction product of step (a) to recover therefrom homogeneous cobalt catalyst and to separate therefrom essentially cobalt-free crude alcohol product which contains 20 wt. % or more of said carbonyl-containing compounds, said catalyst-free crude alcohol product becoming the feed to step b of said catalyzed hydroformylation process.

12. In a process for preparing Oxo alcohols by the catalyzed hydroformylation of olefins which comprises the steps of:(a) hydroformylating a hydrocarbon stream comprising at least one olefin selected from C4, C5, C6, C7, C8, C9, C10, C11, and C12 olefins by reaction of said olefin with carbon monoxide and hydrogen in the presence of a hydroformylation catalyst to produce a crude reaction product which contains carbonyl-containing compounds; (b) hydrogenating said crude reaction product of step (a) to reduce at least a portion of said carbonyl-containing compounds to alcohols; (c) separating the product of step (b) and recovery therefrom an unfinished alcohol product stream; and (d) hydrofinishing (by hydrogenation) the product of step (c) to provide a substantially pure alcohol product; the improvement which comprises conducting step (b) or step (d) or both in the presence of a bulk multimetallic catalyst comprised of at least one Group VIII non-noble metal and at least two Group VIB metals, wherein the ratio of Group VIB to Group VIII metals is from about 10:1 to about 1:10.

13. The process of claim 12, wherein said hydroformylation catalyst is selehcted from rhodium-containing catalyst and cobalt-containing catalyst.

14. The process of claim 13, wherein said hydroformylation catalyst is a cobalt carbonyl catalyst.

15. The process of claim 14, wherein said bulk multimetallic catalyst is a trimetallic catalyst comprised of two Group VIB metals and one Group VIII non-noble metal selected from Ni and Co.

16. The process of claim 15, wherein said Group VIB metals are Mo and W.

17. The process of claim 16, wherein the ratio of Mo to W is about 9:1 to about 1:9.

18. The process of claim 12, wherein said bulk multimetallic catalyst is represented by the formula:(X)b(Mo)c(W)dOz wherein X is a Group VIII non-noble metal, and the molar ratio of b: (c+d) is 0.5/1 to 3/1.

19. The process of claim 18, wherein the ratio of b:(c+d) is 0.75/1 to 1.5/1.

20. The process of claim 12, wherein said bulk multimetallic catalyst is essentially an amorphous material having a unique X-ray diffraction pattern showing crystalline peaks at d=2.53 Angstroms and d=1.70 Angstroms.

21. The process of claim 14, further comprising:(e) demetalling the crude reaction product of step (a) to recover therefrom homogeneous hydroformylation catalyst and to separate therefrom essentially hydroformylation catalyst-free crude alcohol product which contains 20 wt. % or more of said carbonyl-containing compounds, said catalyst-free crude alcohol product becoming the feed to step b of said catalyzed hydroformylation process.