Hydrotreating process employing a pretreated alumina containing material

Description

In one aspect, this invention relates to catalytic hydrotreating of liquid hydrocarbon-containing feed stream, in particular heavy petroleum fractions. In a further aspect, this invention relates to new compositions of matter, suitable as catalysts for hydrotreating processes.
The use of alumina, either unpromoted or promoted with transition metal compounds, for hydrotreating (e.g., demetallizing, desulfurizing, denitrogenating, hydrocracking) liquid hydrocarbon feed streams, which contain metal, sulfur and nitrogen impurities, is well known. The removal of these impurities is desirable because they can poison catalysts in downstream operations such as catalytic cracking, and can cause pollution problems when hydrocarbon products from these feed streams are used as fuels in combustion processes. However, there is an ever present need to develop new alumina-containing materials having improved hydrotreating activity and/or having other improved properties, such as higher crush strength.
SUMMARY OF THE INVENTION
It is an object of this invention to provide effective hydrotreating catalyst compositions. It is another object of this invention to provide processes for prepariag new, effective hydrotreating catalyst compositions. It is a still further object of this invention to provide hydrotreating processes for the removal of sulfur, nickel, vanadium and other impurities from hydrocarbon-containing oils, in the presence of new, effective catalyst compositions. Other objects and advantages will be apparent from the detailed description and the appended claims.
In accordance with this invention, there are provided a process and a composition of matter (suitable as a catalyst composition) comprising alumina and at least one compound of at least one transition metal belonging to Groups VIB, VIIB, VIII or IB of the Periodic Table (as defined in Webster's Collegiate Dictionary, 1977), said composition of matter being prepared by the process comprising the steps of:
(A) impregnating a support material comprising (preferably consisting essentially of) alumina with a solution comprising (preferably consisting essentially of) water and at least one dissolved thiocyanate compound (preferably Group IA and/or Group IIA metal thiocyanate and/or ammonium thiocyanate; more preferably NH.sub.4 SCN);
(B) heating the material obtained in step (A) under such conditions as to at least partially dry said material obtained in step (A);
(C) impregnating the at least partially dried material obtained in step (B) with a solution comprising (preferably consisting essentially of) a liquid solvent (preferably water) and at least one dissolved compound of at least one metal selected from the group consisting of transition metals belonging to Group VB, Group VIB, Group VIIB, Group VIII and Group IB of the Periodic Table of Elements (preferably at least one of Mo, Ni and Co);
(D) heating the material obtained in step (C) at a first temperature so as to at least partially dry said material obtained in step (C);
(E) heating (i.e., calcining) the at least partially dried material obtained in step (D) at a second temperature, which is higher than said first temperature, so as to activate said at least partially dried material obtained in step (D).
Further in accordance with this invention, a substantially liquid (i.e., liquid at the hydrotreating conditions) hydrocarbon-containing feed stream, which also contains compounds of at least one metal (preferably nickel and/or vanadium) and of sulfur as impurities, is simultaneously contacted with a free hydrogen-containing gas (preferably consisting essentially of H.sub.2) and the composition of matter prepared by the process comprising steps (A) through (E), under such hydrotreating conditions as to produce a hydrocarbon-containing stream having reduced levels of metal and sulfur.
Still further in accordance with this invention, there are provided a process and a composition of matter (suitable as a material for a layer in a fixed hydrotreating bed) comprising (preferably consisting essentially of) impregnated, substantially spherical alumina-containing particles, prepared by the process comprising the steps of:
(a) impregnating (i) a starting material of substantially spherical alumina-containing particles which have an initial average particle size (diameter) of at least about 0.05 inch, an initial surface area (determined by the BET/N.sub.2 method; ASTM D3037) of at least about 20 m.sup.2 /g, an initial pore volume (determined by mercury intrusion porosimetry at a pressure ranging from 0 to 50,000 psig) of at least about 0.1 cc/g, and an initial Al.sub.2 O.sub.3 content of at least ahout 80 weight-%, with (ii) a a solution (preferably aqueous) comprising dissolved ammonium thiocyanate; and
(b) heating the material obtained in step (a) at a temperature in the range of from about 500.degree. to about 900.degree. C. for a period of time of at least about 10 minutes (preferably in the range of from about 10 minutes to 20 hours), under such heating conditions as to obtain a material having a higher crush strength than said starting material (wherein the crush strength is measured after exposure of each of the two materials for about 100 hours to a liquid hydrocarbon-containing stream which contains at least about 0.5 weight-% sulfur, under hydrotreating conditions at about 2250 psig total pressure, about 400 psig partial pressure of steam and about 700.degree. F.).
Preferably a drying step (a1) after step (a) is carried out, so as to remove at least a portion of water from the material obtained in step (a). In this preferred embodiment, step (b) is carried out with the material obtained in step (a1). Also preferably, the starting material used in step (a) has a normalized crush strength of at least about 100 lb per inch diameter per particle, and an initial Na content of less than about 3.0 weight-%.
Still further in accordance with this invention, a hydrotreating process is provided wherein a substantially liquid, hydrocarbon containing feed stream, which also contains compounds of at least one metal (preferably Ni and/or V) and of sulfur as impurities, is simultaneously contacted with a free hydrogen containing gas (preferably substantially pure H.sub.2) and a fixed catalyst bed comprising (Y) at least one layer of the composition of matter prepared by the process comprising steps (a) and (b), and optionally also (a1), under such hydrotreating conditions as to produce a hydrocarbon-containing stream having reduced levels of metal (preferably Ni and/or V) and of sulfur.
In a particularly preferred embodiment, said fixed catalyst bed additionally comprises
(Y) at least one layer of catalyst particles [i.e., hydrotreating catalyst particles; different from the particles in layer (X)] comprising a refractory inorganic carrier (preferably alumina) and at least one (i.e., one or a mixture of two or more) hydrogenation promoter selected from the group consisting of transition metals of Groups IIIB, IVB, VB, VIB, VIIB, VIII, IB and IIB of the Periodic Table (as defined in Webster's New Collegiate Dictionary, 1977) and compounds of these metals (preferably Y, La, Ce, Ti, Zr, Cr, Mo, W, Mn, Re, Ni, Co and Cu, and compounds thereof).
In another preferred embodiment of this invention, a fixed catalyst bed (preferably a hydrotreating catalyst bed) is provided comprising
(X) at least one catalyst bed layer of impregnated, substantially spherical alumina-containing particles of this invention, having been prepared by the process composing steps (a) and (b), and optionally also step (a1), as described above; and
(Y) at least one catalyst bed layer of catalyst particles [preferably hydrotreating catalyst particles; different from the particles in layer (X)] comprising a refractory inorganic carrier material and a hydrogenation promoter, as defined immediately above.
In a further preferred embodiment of this invention, said impregnated, substantially spherical alumina-containing particles, which can be used in catalyst bed layer (X), also contain at least one compound of at least one element selected from the group consisting of Y, La, Ce, Ti, Zr, Cr, Mo, W, Mn, Re, Ni, Co, Cu, Zn and P, preferably oxide and/or sulfide of Mo and/or Co and/or Ni (more preferably containing about 0.1-2.0 weight-% Mo) as hydrotreating promoters. In a preferred embodiment, the impregnating solution used in step (a) comprises at least one compound of at least one of the elements listed immediately above.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. I shows the arrangement of a fixed multi-layer catalyst bed used for testing catalysts in hydrotreating processes.
FIG. 2 is a graph showing the dependence of crush strength (determined after use in a hydrotreating test in the presence of steam) of alumina-containing particles on the calcination temperature.
FIG. 3 exhibits pore distribution curves for several alumina-containing particles.

DETAILED DESCRIPTION OF THE INVENTION
Composition prepared by Process Comprising Steps (A) Through (E).
The alumina support material used in step (A) of the preparation of the composition of matter (catalyst composition) of this invention can be any alumina or partially hydrated forms thereof, preferably substantially pure alumina. Generally, the surface area (determined by the BET/N.sub.2 method; ASTM D3037) of said support material is about 20 to about 350 m.sup.2 /g and the pore volume (measured by mercury intrusion porosimetry) is about 0.2 to about 2.0 cc/g. The support material may contain transition metals such as those of Groups IB, IIB, IIIB, IVB, VB, VIB, VIIB and VIII of the Periodic Table, e.g., Mo, Ni, Co or compounds thereof. At present, it is not preferred to have more than only traces of these transition metals present in the alumina-containing support material i.e., the level of these transition metals should be less than about 0.2 weight-%, based on the weight of the entire alumina-containing material (before impregnation).
It is within the scope of this invention (yet presently not preferred) to employ mixtures of alumina with other inorganic refractory materials such as silica, aluminosilicates (such as zeolites), magnesia, titania, zirconia, aluminum phosphate, zirconium phosphate, alumina-silica, alumina-titania, zeolite-alumina, zeolite-silica and the like. Generally, the above-mentioned other refractory materials will not exceed about 10 weight-%, based on the weight of the alumina-containing support material. The alumina support material can be spherical (presently preferred diameter of alumina particles: about 0.2-20 mm, preferably about 0.5-3 mm) or can have cyclindrical, trilobal or quadtrilobal form or can be irregularly shaped.
Any suitable thiocyanate compound can be used as solute in the solution employed in step (A). Non-limiting examples of such thiocyanates are NH.sub.4 SCN, LiSCN, NaSCN, KSCN, CsSCN, RbSCN, Mg(SCN).sub.2, Ca(SCN).sub.2, and other alkaline earth metal thiocyanates, preferably NH.sub.4 SCN. It is understood that these thiocyanates can be applied as hydrates. It is also understood that the ammonium group in ammonium thiocyanate can be alkyl-substituted (presently not preferred).
The concentration of the thiocyanate compound in the aqueous impregnating solution used in steps (A) generally is in the range of from about 1 to about 200 grams per liter (g/l) solution, preferably from about 10 to about 100 g/l more preferably from about 3 to about 80 g/l. The weight ratio of the alumina-containing support material to the thiocyanate-containing impregnating solution employed in steps (A) generally is in the range of from about 1:20 to about 5:1 (depending on the concentration of the thiocyanate-containing solution), preferably from about 1:5 to about 1:1. The impregnation time in step (A) should be long enough to ensure that the alumina-containing support materials are substantially penetrated by the impregnating solution. Generally, the impregnation time is in the range of from about 0.5 to about 60 minutes, preferably from about 1 to about 10 minutes. The temperature during impregnation in step A can be ambient (e.g., about 60.degree.-75.degree. F.) or higher (e.g., about 80.degree.-200.degree. F.).
Heating steps (B) and (D) are generally carried out in an oxidizing gas atmosphere (preferably in air) or an inert gas atmosphere, at a temperature ranging from about 40.degree. C. to about 300.degree. C. so as to remove the greatest portion of water from the mixture obtained in the preceding step. The preferred temperature for step (B) is in the range of from about 80.degree. C. to about 300.degree. C.; the preferred temperature for step (D) is in the range of from about 50.degree. C. to about 200.degree. C. Vacuum conditions may be employed but are presently not preferred. The substantially dried material obtained in step (B) generally contains less than about 5 weight-% water. The at least partially dried material obtained in step (D) generally contains less than 20 weight-% water. The rate of heating is controlled so as to avoid surges of water vapor that can cause the impregnating solution to splatter and to excessively accumulate in certain surface regions of the solid support material. Depending on the heating temperature and specific heating conditions (such as extent of gas movement and thickness of the solid layer to be dried), the heating time ranges generally from about 0.5 hour to about 100 hours, preferably from about 1 hour to about 30 hours.
Impregnating step (C) can be carried out in any suitable manner with any suitable dissolved transition metal compound that is at least partially soluble in the solvent of the solution. The solvent can be an organic solvent such as methanol, ethanol, higher alcohols, carboxylic acids such as acetic acid, acetone, esters and similar polar liquids. Preferably the solvent is water. Non-limitative examples of metals contained in said dissolved metal compound are Cr, Mo, W, Re, Co, Ni, Cu and mixtures of two or more; preferably Mo, Co, Ni and mixtures of two or three of these metals. The transition metal compounds can be halides (e.g., chlorides), nitrates, sulfates, bisulfates, bicarbonates, carboxylates (e.g., acetate, oxalate, citrate and the like), coordination complexes (e.g., ammino complexes of Ni and Co salts and the like), homo- and hetropolyacids and their salts (e.g., ammonium molybdates), and the like. It is understood that these compound can be applied as hydrates, e.g., Ni(NO.sub.3).sub.3.6H.sub.2 O, Co(NO.sub.3).sub.3.6H.sub.2 O and (NH.sub.4).sub.2 Mo.sub.7 O.sub.24.4H.sub.2 O (all three compounds being presently preferred).
Any suitable concentration of the at least one transition metal compound in the impregnating solution of steps (C) and any suitable weight ratio of the at least partially dried material from step (B) to said impregnating solution can be applied. This concentration and weight ratio can vary widely, depending on what the desired level of transition metal promoter in the finished catalyst composition is. Generally the combined concentration of all metal compounds in the impregnating solution of step (C) is in the range of from about 0.01 to about 5.0 mol/l preferably from about 0.05 to about 3.0 mol/l. The weight ratio of the at least partially dried material obtained in step (B) to the impregnating solution generally is in the range of from about 1:100 to about 101 preferably from about 1:10 to about 2:1. Other solvents (which may aid in the dissolving of the metal compounds) such as acids (e.g., citric acid, phosphoric acid), borates and phosphates may also be present in the impregnating solution.
Step (C) can be carried out at room temperature (e.g., 60.degree.-75.degree. F.) as at elevaled temperatures (e.g., 80.degree.-200.degree. F.), with or without agitation. The at least partially dried material obtained in steps (B) can be soaked with the impregnating solution (with or without agitation) or can be mixed for any suitable time (generally about 1 minute to about 5 hours, preferably about 0.1-2 hours). Excess impregnating solution can be drained. The impregnating solution can also be sprayed onto the at least partially dried material from step (B). Presently, soaking of the material obtained in step (B) with the impregnating solution and subsequent draining of excess solution is preferred.
Even though it is preferred to employ substantially clear aqueous solutions in steps (A) and (C), it is within the scope of this invention to use aqueous solutions having solid particles dispersed therein. In this case, the solutions plus dispersed particles can be used "as is" in steps (A) and (C), or, preferably, the dispersed solid particles are separated from the solutions by any suitable separation means, such as filtration, centrifugation or settling and subsequent draining, before the solutions are used for the impregnation of alumina.
The preferred heating (calcining) conditions in step (E) comprise heating in a non-reducing gas atmosphere, a temperature ranging from about 300.degree. C. to about 700.degree. C. (more preferably from about 400.degree. C. to about 600.degree. C.) and a heating time ranging from about 1 to about 10 hours. Presently preferred specific calcining conditions are described in Example I (Catalyst A). Generally, the heating is carried out in a free oxygen containing atmosphere, preferably air. But other non-reducing gases, e.g., nitrogen, helium, neon, argon, krypton, xenon or mixtures thereof, may also be employed.
The terms "activate" and "activation" as used herein means that the calcined catalyst composition of this invention is a more effective catalyst for hydrotreating reactions, particularly hydrodemetallization and hydrodesulfurization of liquid hydrocarbon-containing feed streams, than the at least partially dried mixture obtained in preceding step (D). Preferably transition metal compounds contained in the at least partially dried material obtained in step (D) are at least partially converted to metal oxides in step (E).
The calcined composition of matter of this invention obtained in step (E) generally contains from about 0.1 to about 25 weight-% transition metal, and preferably contains from about 0.3 to about 8.0 weight-% transmition metal. The surface area (determined by the BET/N.sub.2 method; ASTM D3037) of the calcined catalyst compositions of matter of this invention generally is in the range of from about 20 to about 350 m.sup.2 /g, preferably in the range of from about 100 to about 250 m.sup.2 /g. The pore volume (determined by mercury intrusion using an Autopore 9200 instrument of Micromeretics, Norcross, Ga.) generally is in the range of from about 0.2 to about 2.0 cc/g. The compositions of matter of this invention can be spherical or can be compacted into various shapes (e.g., cylindrical, trilobal etc) for convenient shipping and use in fixed catalyst beds.
In one embodiment, the composition of matter (catalyst composition) of this invention obtained in step (E) is presulfided by the additional step (F) of contacting the calcined compositions of matter with at least one suitable sulfur compound under such conditions as to at least partially convert transition metal compounds (preferably oxides) contained in the calcined catalyst composition to transition metal sulfides. This can be accomplished by passing a sulfur-containing oil (preferably gas oil) or solutions of COS or of mercaptans or of organic sulfides, e.g., in hydrocarbon solvents, over the composition of matter at an elevated temperature (e.g., at about 300.degree.-650.degree. F.), generally in the presence of hydrogen gas; or a gaseous mixture of hydrogen and hydrogen sulfide (e.g. at a volume ratio of about 10:1) can be passed over the catalyst composition at an elevated temperature, preferably 1-15 hours at about 400.degree. F. and then 1-15 hours at about 700.degree. F. This presulfiding step is particularly desirable when the composition of matter (catalyst composition) of this invention is used for hydrotreating or hydrocracking of liquid hydrocarbon-containing feed streams.
The composition of matter obtained in step (E) can also be heated in a reducing gas such as H.sub.2, CO methane and the like or gas mixtures containing H.sub.2, CO, methane and the like, under such conditions as to at least partially (preferably substantially) convert transition metal compounds to the metallic form (e.g. Ni metal). The reducing treatment is presently not preferred.
Hydrotreating Process
The composition of matter of this invention can be used as a catalyst composition for a variety of hydrocarbon conversion reactions. In one preferred embodiment of this invention, the catalyst composition of this invention is used as a catalyst for hydrotreating substantially liquid hydrocarbon-containing feed streams, which also contain compounds of sulfur, nickel and/or vanadium as impurities, and generally also asphaltenes, coke precursors (measured as Ramsbottom carbon residue) and nitrogen compounds. Suitable hydrocarbon containing feed streams include crude oil and heavy fraction thereof, heavy oil extracts, liquid coal pyrolyzates, heavy liquids from coal liquification, heavy liquids obtained from tar sands, shale oil and heavy shale oil fractions. The catalyst compositions are particularly suited for treating heavy oil residua, which generally have an initial boiling point in excess of about 400.degree. F., preferably in excess of about 600.degree. F., contain about 5-1000 ppmw (parts by weight per million by weight of feed stream) of vanadium, about 3-500 ppmw of nickel, about 0.3-5 weight-% sulfur and about 0.2-2 weight-% nitrogen, and have an API.sub.60 gravity of about 5-30.
The hydrotreating process of this invention employing the catalyst composition of this invention is carried out in any apparatus wherein an intimate contact of the catalyst composition with said hydrocarbon-containing feed stream and a free hydrogen containing gas is achieved, under such conditions as to produce a hydrocarbon-containing product having a reduced levels of nickel and/or vanadium and sulfur. Generally, a lower level of nitrogen and Ramsbottom carbon residue and a higher value of API.sub.60 gravity are also attained in this hydrotreating process. The hydrotreating process can be carried out using a fixed catalyst bed (presently preferred) or a fluidized catalyst bed or a moving catalyst bed or an agitated slurry of the catalyst in the oil feed (hydrovisbreaking operation). The hydrotreating process can be carried out as a batch process or, preferably, as a continuous process, more preferably in a tubular reactor containing one or more fixed catalyst beds or in a plurality of fixed bed reactors in parallel or in series.
The catalyst composition of this invention can be used in said hydrotreating process alone in a reactor or may be used in combination with essentially unpromoted refractory materials such as alumina, silica, titania, magnesia, silicates, metal aluminates, alumino-silicates (e.g., zeolites), metal phosphates and mixtures of these materials. Alternating layers of the refractory material and of the catalyst composition can be used, or the catalyst composition can be mixed with the refractory material. Use of the refractory material with the catalyst composition provides for better dispersion of the hydrocarbon-containing feed stream. Also, other catalysts such as known hydrogenation and desulfurization catalysts (e.g., NiO/MoO.sub.3, CoO/MoO.sub.3 and NiO/CoO/MoO.sub.3 on silica or titania) may be used with the catalyst composition of this invention to achieve simultaneous demetallization, desulfurization, denitrogenation, hydrogenation and hydrocracking, if desired. In one embodiment of said hydrocarbon hydrotreating process, the catalyst composition has been presulfided, as described above, before being used.
Any suitable contact (reaction) time between the catalyst composition, the hydrocarbon-containing feed stream and hydrogen gas can be utilized. In general, the reaction time will range from about 0.05 hours to about 10 hours. Preferably, the reaction time will range from about 0.4 to about 5 hours. Thus, the flow rate of the hydrocarbon-containing feed stream should be such that the time required for the passage of the mixture through the reactor (residence time) will preferably be in the range of about 0.4 to about 5 hours. In a continuous fixed bed operation, this generally requires a liquid hourly space velocity (LHSV) in the range of about 0.10 to about 20 cc of feed per cc of catalyst per hour, preferably from about 0.2 to about 2.5 cc/cc/hr.
The hydrotreating process employing the catalyst composition of the present invention can be carried out at any suitable temperature. The temperature will generally be in the range of about 250.degree. C. to about 550.degree. C. and will preferably be in the range of about 350.degree. C. to about 450.degree. C. Higher temperatures do improve the removal of metals, but temperatures which will have adverse effects on the hydrocarbon-containing feed stream, such as excessive coking, will usually be avoided. Lower temperatures can generally be used for lighter feeds.
Any suitable pressure may be utilized in the hydrotreating process of this invention. The reaction pressure will generally be in the range of about atmospheric pressure (0 psig) to up to about 5,000 psig. Preferably, the pressure will be in the range of about 100 to about 2500 psig. Higher pressures tend to reduce coke formation but operating at high pressure may be undesirable for safety and economic reasons.
Any suitable quantity of hydrogen can be added to the hydrotreating process. The quantity of hydrogen used to contact the hydrocarbon containing feed stock will generally be in the range of about 100 to about 10,000 standard cubic feed H.sub.2 per barrel of the hydrocarbon containing feed stream and will more preferably be in the range of about 1000 to about 6000 standard cubic feed H.sub.2 per barrel of the hydrocarbon containing feed stream.
In general, the catalyst composition is utilized primarily for demetallization until a satisfactory level of metals (Ni, V) removal is no longer achieved. Catalyst deactivation generally results from the coating of the catalyst composition with coke and metals removed from the feed. It is possible to remove the metals from the catalyst. But it is generally contemplated that once the removal of metals falls below a desired level, the spent (deactivated) catalyst will simply be replaced by fresh catalyst.
The time in which the catalyst composition of this invention will maintain its activity for removal of metals and sulfur will depend upon the metals concentration in the hydrocarbon containing feed streams being treated. Generally the catalyst composition can be used for a period of time long enough to accumulate about 20-200 weight-% of metals, mostly Ni and V, based on the initial weight of the catalyst composition, from the hydrocarbon containing feed. In other words, the weight of the spent catalyst composition will be about 20-200% higher than the weight of the fresh catalyst composition.
Generally, at least a portion of the hydrotreated product stream having reduced metal and sulfur contents is subsequently cracked in a cracking reactor, e.g. in a fluidized catalytic cracking unit, under such conditions as to produce lower boiling hydrocarbon materials (i.e., having a lower boiling range at 1 atm. than the feed hydrocarbons) suitable for use as gasoline, diesel fuel, lubricating oils and other useful products. It is within the scope of this invention to hydrotreat said product stream having reduced metal and sulfur contents in one or more processes using different catalyst compositions, such as alumina-supported NiO/MoO.sub.3 or CoO/MoO.sub.3 catalysts, for further removal of sulfur and other impurities, before the product stream is introduced into the cracking reactor.
A further embodiment of this invention is a hydrofining (hydrotreating) process comprising the step of introducing at least one thermally decomposable metal compound into the hydrocarbon containing feed stream prior to its being contacted with the catalyst composition of this invention. The metal in the decomposable metal compound is selected from the group consisting of the metals of Group IV-B, Group V-B, Group VI-B, Group VII-B, Group VIII and Group IB of the Periodic Table of Elements. Preferred metals are molybdenum, tungsten, manganese, chromium, zirconium and copper. Molybdenum is a particularly preferred metal which may be introduced as a carbonyl, acetylacetonate, carboxylate having 1-12 C atoms per molecule (e.g., acetate, octoate, oxalate), naphthenate, mercaptide, dithiophosphate or dithiocarbamate. Molybdenum hexacarbonyl, molybdenum dithiophosphate and molybdenum dithiocarbamate are particularly preferred additives. The life of the catalyst composition and the efficiency of the demetallization process is improved by introducing at least one of the above-cited decomposable metal compounds into the hydrocarbon-containing feed, which also contains metal such as nickel and vanadium. These additives can be added continuously or intermittently and are preferably added at a time when the catalyst composition of this invention has been partially deactivated so as to extend its life.
Any suitable concentration of these additives may be added to the hydrocarbon-containing feed stream. In general, a sufficient quantity of the additive will be added to the hydrocarbon-containing feed stream to result in a concentration of the metal (preferably molybdenum) in said decomposable compounds ranging from about 1 to about 1000 parts per million and more preferably in the range of about 5 to about 100 parts per million in the feed stream.
Impregnated, Substantially Spherical Alumina-Containing Particles
Any suitable substantially spherical alumina-containing particles which have the following initial parameters can be used as said starting material for step (a): average particle diameter of at least about 0.05 inch, preferably in the range of from about 0.05 to about 1.5 inch, more preferably from about 0.1 to about 1.0 inch; surface area (determined by the BET/N.sub.2 method; ASTM D3037) of at least about 20 m.sup.2 /g, preferably in the range of from about 40 to about 600 m.sup.2 /g, more preferably in the range of from 100 to about 400 m.sup.2 /g; a pore volume, as determined by mercury intrusion porosimetry (carried out at room temperature and a mercury pressure varying from 0 psi to about 60,000 psi, using an Autopore 9200 instrument of Micromeritics, Norcross, Ga.), of at least about 0.1 cc/g, preferably in the range of from about 0.2 to about 1.0 cc/g., more preferably from about 0.3 to about 0.7 cc/g; and content of alumina, which generally is a mixture of gamma-alumina and amorphous alumina, of at least about 80 weight-% Al.sub.2 O.sub.3, preferably in the range of from about 90 to about 99 weight-% Al.sub.2 O.sub.3, more preferably from about 93 to about 98 weight-% Al.sub.2 O.sub.3. The preferred starting material has a normalized crush strength per particle, determined as side plate crush strength by means of a mechanical force gauge, such as the one described in Example I, of at least 100 lb. per inch diameter per particle, more preferably in the range of from about 100 to about 400 lb. per inch diameter per particle; and a Na content of less than about 3.0 weight-%, more preferably below about 2.0 weight-% Na, most preferably below about 0.5 weight-% Na. A presently particularly preferred starting material is a commercially available spherical, alumina-containing Claus catalyst material that is marketed by the Aluminum Company of America, Pittsburgh, Pa. under the product designation of S-100 (see Example V).
Preparation step (a), as described above, can be carried out in any suitable manner. The solvent in the impregnating solution used in step (a) generally comprises water, and preferably consists essentially of water. Suitable solvents which can be used besides water are alcohols such as methanol, ethanol, ethylene glycol and the like, acetone, esters such as ethyl acetate, and the like. However, these non-aqueous solvents are presently not preferred. The concentration of ammonium thiocyanate in the impregnating solution of step (a) can be in the range of from about 0.05 to about 5 mol/l preferably in the range of from about 0.1 to about 1.0 mol/l (i.e., mols NH.sub.4 SCN per liter solution).
The impregnation of the alumina-containing starting material with the impregnating solution can be carried out in any suitable manner. Preferably the starting material is soaked with the NH.sub.4 SCN-containing impregnating solution, more preferably with agitation such as mechanical stirring, for a period of time long enough (preferably about 0.2-2 hours) to allow dissolved ammonium thiocyanate to penetrate into the substantially spherical, alumina-containing particles of the starting material, more preferably to the core of these particles. Any suitable weight ratio of said starting material to the impregnating solution can be employed. Preferably, the weight ratio of said starting material to said impregnating solution will be in the range of from about 0.1:1 to about 2.0:1, more preferably from about 0.3:1 to about 1.2:1. Even though presently not preferred, other impregnating methods can be applied, such as spraying of the NH.sub.4 SCN-containing impregnating solution onto the substantially spherical, alumina-containing particles of the starting material.
Even though the material obtained in step (a) can be directly processed in step (b), it is presently preferred to substantially dry the impregnated material obtained in step (a) in drying step (a1). The drying step (a1) is generally carried out in air or an inert gas, at a temperature ranging from about 25.degree. C. to about 200.degree. C. (preferably 50.degree.-100.degree. C.) so as to remove the greatest portion of water from the mixture obtained in step (b). Vacuum conditions may be employed but are presently not preferred. The at least partially dried mixture generally contains less than about 20 weight-% water. The rate of drying is controlled so as to avoid surges of water vapor that can cause the impregnating solution to splatter and can cause the particles to crack. Depending on the drying temperature and specific drying conditions (such as extent of air movement; thickness of the solid layer to be dried), the drying time ranges generally from about 0.5 hour to about 100 hours, preferably from about 1 hour to about 30 hours.
The impregnated alumina-containing material obtained in step (a), or alternatively step (a1), is heated (calcined) at a temperature in the range of from about 500.degree. to about 900.degree. C., preferably from about 550.degree. to about 800.degree. C., more preferably from about 600.degree. to about 750.degree. C. The heating time is at least 10 minutes, preferably in the range of from about 10 minutes to 20 hours, more preferably from about 0.5 to about 10 hours. The pressure can be atmospheric (preferred) or subatmospheric or superatmospheric. The heating process can be carried out in a free oxygen containing gas atmosphere, such as air, or in an inert or in a reducing gas atmosphere. Presently, heating in an O.sub.2 -containing gas is preferred. The gas atmosphere may contain water vapor, but the amount of water vapor should be minimized to less than about 10 volume percent.
Generally the above-described heating (calcining) of the impregnated spherical, alumina-containing material results in a tolerable decrease in surface area, in a slight increase in total pore volume, but in a substantial increase of the pore volume in pores having a pore diameter in the 40-200 Angstroms (A) range. Preferably, the impregnated, substantially spherical alumina-containing particles obtained by the preparation process of this invention have a pore volume of pores in the 40-200 A pore diameter range in excess of about 50%, more preferably from about 50 to about 90% of the total pore volume. Preferably, the total BET/N.sub.2 surface area of the impregnated, substantially spherical particles of this invention is in the range of from about 50 to about 300 m.sup.2 /g, and the total pore volume (determined by mercury porosimetry, discussed above) is in the range of from about 0.3 to about 0.8 cc/g.
The crush strength of the impregnated, substantially spherical alumina-containing particles of this invention is preferably measured after they have been used in a hydrotreating process in the presence of water and sulfur compounds, as has been described above and also in Example IV, so as to determine the retention of initial crush strength under these severe hydrotreating conditions (about 2250 psi total pressure, about 400 psi partial pressure of steam, about 700.degree. F., about 100 hours; with at least about 0.5 weight-% sulfur in the hydrocarbon-containing feed). It is believed that the combination of hydrogen, steam and sulfur compounds (resulting in H.sub.2 S generation under catalytic hydrotreating conditions) is particularly detrimental to the crush strength of these particles. The thus determined crush strength generally exceeds 150 lb. per inch diameter per particle and preferably is in the range of about 150 to about 350 lb./inch/particle.
The impregnated, substantiaIly spherical alumina-containing particles of this invention can be promoted with at least one element or compound at least one element (i.e., one or mixture of two or more) selected from the group consisting of Y, La, Ce, Ti, Zr, Hf, Cr, Mo, W, Mn, Re, Ni, Co, Cu, Zn, P (as phosphite and/or phosphate), preferably Mo, Ni and Co, more preferably Mo. The total promoter level generally is relatively low and suitably ranges from about 0.01 to about 3.0 weight-% of said at least one element (i.e. are element or mixture of two or more elements), preferably from about 0.1 to about 2.0 weight-%, more preferably from about 0.2 to about 1.0 weight-% of said at least one element (most preferably Mo).
Any suitable technique for promoting the particles of this invention can be employed. Preferably the impregnating solution used in step (a) contains one or more of the above-described promoters besides dissolved NH.sub.4 SCN. The thus obtained particles, which additionally contain at least one promoter compound then undergo step (b) optionally after step (a1), as described above. It is, of course, possible (yet presently not preferred) to carry out step (a) without having any transition metal and/or phosphorus promoter compound present in the impregnating solution, and to impregnate the calcined material obtained in step (b) with a solution containing at least one promoter compound, followed by drying and calcining (preferably at about 500.degree.-900.degree. C.) of the thus twice-impregnated material (so as to at least partially convert the at least one transition metal compound to oxides of said metal). Generally the crush strength of the impregnated, substantially spherical alumina-containing particles is not substantially affected by the presence of one or more promoters.
Fixed Catalyst Bed
In accordance with this invention, a fixed catalyst bed, suitable for hydrotreating substantially liquid hydrocarbon-containing feed streams, which also contain sulfur and metal compounds (as has been described earlier for another embodiment of this invention), is provided comprising at least one layer (X) of the impregnated, substantially spherical alumina-containing material of this invention, prepared by the process comprising steps (a), (b), and optionally, (a1).
In a preferred embodiment of this invention, the fixed catalyst bed comprises at least one layer (X), as described above, and also at least one layer (Y) of catalyst particles, different from those in layer (X). The catalyst particles in layer (Y) generally comprise an inorganic refractory carrier. Non-limiting examples of such inorganic refractory carrier materials are those that comprise (preferably consist essentially of) alumina (preferred), aluminum phosphate, silica, titania, zirconia, zirconium phosphate, ceria, boria, magnesia, silica-alumina, titania-silica, titania-alumina. In addition to the carriers, the catalyst particles in catalyst bed layer (Y) comprise at least one promoter selected from compounds of metals of Groups IIIB, IVB, VB, VIB, VIIB, VIII, IB and IIB of the Periodic Table. Presently preferred promoters are compounds of metals selected from the group consisting of Y, La, Ce, Ti, Zr, Cr, Mo, W, Mn, Re, Ni, Co and Cu, more preferably oxides and/or sulfides of these metals, most preferably Mo, Ni, Co, and mixtures of any of these metal oxides and sulfides. Phosphorus compounds of these metals can also be present. Generally the total level of promoter ranges from about 0.5 to about 30 weight-%, preferably from about 1 to about 15 weight-%, based on the elemental metal. Generally the BET/N.sub.2 surface area of the particles in layer (Y) is in the range of from about 50 to about 500 m.sup.2 /g, and their pore volume (measured by mercury porosimetry) is in the range of from about 0.2 to about 2.0 cc/g.
The catalyst particles in layer (Y) can be prepared by any suitable technique such as by impregnation of the carrier (preferably alumina) with one or more solutions containing one or more compounds of the promoter metals (plus, optionally, one or more compounds of phosphorus) and subsequent drying and calcining (this method presently being preferred) as has been described for promoted particles in layer (X); or by coprecipitation e.g., of hydrogels of alumina and promoter metal (e.g., Ni, Co, Mo), followed by drying and calcining. Suitable commercially available catalyst materials for layer (Y) are described in Example IV.
Layers (X) and (Y) can be arranged in the fixed catalyst bed of this invention in any suitable manner. In one preferred embodiment, layer (X) is placed as support layer below at least one catalyst layer (Y). In another embodiment, layer (X) is placed as a cover layer on top of at least catalyst layer (Y). In a further embodiment, catalyst layer (Y) is placed between at least two layers (X). In a still further embodiment, in which at least three layers (X) and at least two catalyst layers (Y) (which are different from each other) are employed, one layer (X) is placed on top of said at least two catalyst layers (Y), one layer (X) is placed as interlayer between two different catalyst layers (Y), and a third layer (X) is placed below said at least two lower catalyst layer (Y). Another suitable catalyst bed arrangement is shown in FIG. 1. The weight ratio of each catalyst layer (X) to each catalyst layer (Y) is generally in the range of from about 1:100 to about 1:1, preferably from about 1:20 to about 1:5.
The dimensions of catalyst bed layer (X) comprising the substantially spherical alumina-containing particles obtained by the above-described heating process are not considered critical and depend on the dimension of the hydrotreating reactor that holds the fixed catalyst bed. Generally the height of each layer (X) ranges from about 1 to about 50 feet in commercial hydrotreating operations. It is within the scope of this invention to have additionally inert particles present (up to 50 weight-%) in layer (X), such as shaped inert ceramic particles. The height of each catalyst layer (Y) can vary widely, depending on the particular reactor dimensions.
If desired, the fixed catalyst bed of this invention can be sulfided by treatment with a fluid stream that contains sulfur compounds, generally prior to said hydrotreating process. Non-limiting examples of such fluid streams are solutions of mercaptans, of mercaptoalcohols, of organic sulfides or of organic disulfides in a suitable organic solvent (such as gas oil and other petroleum fractions), and gas streams that comprise H.sub.2 S, such as mixtures of H.sub.2 and H.sub.2 S. This sulfiding procedure is generally carried out at an elevated temperature (preferably at about 400.degree.-700.degree. F.) for a period of time sufficient (preferably from about 0.5-20 hours) so as to convert at least a portion of compounds of one or more metals contained in particles of layer (Y), and optionally also in particles of layer (X), to sulfides of said one or more metals.
In general, the fixed catalyst bed of this invention is utilized primarily for demetallization and desulfurization. The time in which the fixed catalyst bed of this invention will maintain its activity for the above process will depend upon the hydrotreating conditions and the composition of the hydrocarbon-containing feed. Generally, the temperature of the hydrotreating process is gradually increased to compensate for loss of catalyst activity due to fouling (e.g., due to deposition of coke and metals as the catalyst). The entire fixed catalyst bed or one or more layers of the fixed catalyst bed can, if desired, be regenerated when the catalytic activity has dropped below a desired level. Catalyst regeneration can be carried in-situ by discontinuing the flow of hydrogen and of the hydrocarbon-containing feed streams, purging the fixed bed reactor with an inert gas (e.g., N.sub.2), and then heating the fixed catalyst bed in a free oxygen-containing gas atmosphere (such as air), under such conditions as to remove carbonaceous materials and to at least partially convert sulfides of transition metals such as Mo, Co and/or Ni back to their oxides and/or phosphates. Preferably, however, the fixed bed layers are removed from the cooled hydrotreating reactor after said purging and are transferred to another reactor where the catalyst regeneration takes place. Generally the catalyst regeneration step is carried out at about 400.degree.-600.degree. C. and at a pressure of about 0-1,000 psig.
The following examples are presented in further illustration of the invention and are not to be considered as unduly limiting the scope of this invention.
EXAMPLE I
This example illustrates the preparation of various promoted alumina-containing materials, useful as catalyst for hydrogenation and hydrotreating processes.
Catalyst 1 (Control) was prepared by mixing 20 grams of spherical alumina (diameter 1-2 mm, BET/N.sub.2 surface area: 130 m.sup.2 /g; pore volume, as determined by mercury intrusion porosimetry: 1.0 cc/g; supplied by Alcoa Chemicals Division of Aluminum Company of America, Pittsburg, Pa.) with about 22 g of an aqueous impregnating solution containing 2.94 g citric acid, 2.94 g (NH.sub.4).sub.6 Mo.sub.7 O.sub.24 4H.sub.2 O, 0.79 g Ni(NO.sub.3).sub.2.6H.sub.2 O and 0.79 g Co(NO.sub.3).6H.sub.2 O. The mixture of alumina and impregnating solution was air-dried and then calcined at 800.degree. F. for 3 hours. Catalyst 1 contained 0.7 weight-% Ni, 0.7 weight-% Co and 7.0 weight-% Mo.
Catalyst 2 (Control) was prepared by first soaking 26.5 g of spherical alumina (see above) with a pretreating solution containing 5 g NH.sub.4 HSO.sub.4 in 100 cc deionized water, for about 3 minutes at room temperature. Excess pretreating solution was decanted. The thus pretreated alumina was dried, soaked with about 29 g of an impregnating solution containing 3.7 g citric acid, 3.7 g (NH.sub.4).sub.2 Mo.sub.7 O.sub.24.4H.sub.2 O, 1.0 g Ni(NO.sub.3).sub.2.6H.sub.2 O and 1.0 g Co(NO.sub.3).sub.2.6H.sub.2 O, air-dried, and calcined at 800.degree. F. for 3 hours. Catalyst 2 contained 0.7 weight-% Ni, 0.7 weight-% Co and 7.0 weight-% Mo.
Catalyst 3 (Control) was prepared essentially in accordance with the method for making Catalyst 2, except that the pretreating solution contained 5 g (NH.sub.4).sub.2 SO.sub.4 (in lieu of NH.sub.4 HSO.sub.4) in 100 cc H.sub.2 O. Catalyst 3 contained 0.7 weight-% Ni, 0.7 weight-% Co and 7.0 weight-% Mo.
Catalyst 4 (Invention) was prepared essentially in accordance with tbe method for making Catalyst 2, except that the pretreating solution contained 5 g NH.sub.4 SCN (in lieu of NH.sub.4 HSO.sub.4) in 100 cc H.sub.2 O. Catalyst 4 containing 0.7 weight-% Ni, 0.7 weight-% Co and 7.0 weight-% Mo.
Catalyst 5 (Control) was prepared essentially in accordance with the method for making Catalyst 1, except that the aqueous impregnating solution additionally contained 0.75 grams of NH.sub.4 SCN. Thus, Catalyst 5 was prepared by simultaneous impregnation with NH.sub.4 SCN and compounds of Mo, Ni and Co (rather than by sequential impregnation as was done for making Catalyst 4). Catalyst 5 contained 0.7 weight-% Ni, 0.7 weight-% Co and 7.0 weight-% Mo.
Catalyst 6 (Control) was prepared essentially in accordance with the method for making Catalyst 1, except that 6.9 g of Catalyst 1 (containing 0.7 weight-% Ni, 0.7 weight-% Co and 7.0 weight-% Mo) was soaked for 3 minutes with a solution of 1.25 g NH.sub.4 SCN in 23.75 g deionized water. Excess NH.sub.4 SCN solution was decanted, and the NH.sub.4 SCN-soaked material was dried with a heat lamp and calcined in air at 800.degree. F. for 3 hours. Control Catalyst 6 differed from Invention Catalyst 4 in that Catalyst 6 was prepared by post-treatment with NH.sub.4 SCN (whereas Catalyst 4 was prepared by pretreatment of the alumina support before impregnation with Ni, Co and Mo).
EXAMPLE II
In this example, the automated experimental setup for investigating the hydrofining of heavy oils in accordance with the present invention is described. Oil was pumped downward through an induction tube into a trickle bed reactor, 28.5 inches long and 0.75 inches in diameter. The oil pump used was a reciprocating pump with a diaphragm-sealed head. The oil induction tube extended into a catalyst bed (located about 3.5 inches below the reactor top) comprising a top layer of about 25 cc of low surface area .alpha.-alumina (14 mesh alundum; surface area less than 1 m.sup.2 /gram), a middle layer of 13 cc (6.9 g) of one of the hydrofining catalysts described in Example I mixed with 57 cc of 36 mesh alundum, and a bottom layer of about 15 cc of alundum.
The heavy oil feed was a mixture of 50 volume-% 400 F+ Hondo residium and 50 volume-% light cycle oil. The feed contained about 3.1 weight-% sulfur, about 54 ppmw (parts per million by weight) nickel and about 124 ppmw vanadium.
Hydrogen was introduced into the reactor through a tube that concentrically surrounded the oil induction tube but extended only to the reactor top. The reactor was heated with a 3-zone furnace. The reactor temperature was measured in the catalyst bed at three different locations by three separate thermocouples embedded in axial thermocouple well (0.25 inch outer diameter). The liquid product oil was collected every day for analysis. The hydrogen gas was vented. Vanadium and nickel contents were determined by plasma emission analysis and the sulfur content was measured by X-ray fluorescence spectrometry.
EXAMPLE III
This example illustrates the removal of metals (Ni, V) and sulfur from the heavy oil feed (see Example II) by hydrotreatment in the presence of Catalysts 1-6. Pertinent process conditions were: LHSV of about 1.0 cc oil/cc catalyst/hr; hydrogen flow rate of about 2500 per cubic feet H.sub.2 per barrel oil; reaction pressure of about 2250 psig; and reaction temperature of about 700.degree. F. Catalysts 1-6 had been presulfided (before the hydrotreating tests) by heating in a mixture of H.sub.2 and H.sub.2 S (H.sub.2 /H.sub.2 S volume ratio was 10:1.4) at about 400.degree.-700.degree. F. for about 8 hours. Pertinent hydrotreating test results are summarized in Table I.
TABLE I______________________________________Days on Product AnalysisCatalyst Stream Wt % S ppmw (Ni + V)______________________________________1 1 1.28 59.3(Control) 2 1.55 71.7 3 1.66 74.4 4 1.93 88.5 Average 1.6 742 1 1.51 74.4(Control) 2 1.63 71.1 3 1.70 84.4 4 1.65 67.0 Average 1.6 743 1 1.54 80.7(Control) 2 1.81 88.1 3 1.78 77.2 4 1.91 84.2 Average 1.8 834 1 1.21 56.6(Invention) 2 1.38 62.0 3 1.53 69.6 4 1.50 63.3 Average 1.4 635 1 2.92 58.6(Control) 2 1.54 60.7 3 1.50 65.8 4 2.35 78.9 Average 2.1 666 1 3.07.sup.1 44.1.sup.1(Control) 2 1.56 54.73 pump failure; test terminated6 1 2.83 63.4(Control) 2 2.36 75.6Repeat 3 3.36.sup.1 78.8 4 1.96 86.0 Average 2.4 76______________________________________ .sup.1 results considered erroneous; not included in Average.
Data in Table I clearly show that, unexpectedly, Invention Catalyst 4 (wherein alumina support had been pretreated with NH.sub.4 SCN before impregnation with Ni, Co and Mo) was consistently more effective in removing sulfur and metals from the oil feed than Control Catalyst 1 (no pretreatment of alumina support) and Control Catalysts 2 and 3 (wherein alumina had been pretreated with NH.sub.4 HSO.sub.4 and (NH.sub.4).sub.2 SO.sub.4, respectively). Furthermore, Invention Catalyst 4 generally was also more effective as desulfurization/demetallization catalyst than Control Catalyst 5 (prepared by simultaneous impregnation with NH.sub.4 SCN and compounds of Ni, Co and Mo) and Control Catalyst 6 (prepared by post-treatment of Ni/Co/Mo-impregnated alumina with NH.sub.4 SCN).
EXAMPLE IV
This example illustrates the evaluation of catalyst bed support particles in oil hydrotreating tests, in the presence of steam. The purpose of this evaluation procedure is to determine the hydrodemetallization activity and the retention of crush strength of these support particles under severe hydrotreating conditions, in the presence of steam and sulfur compounds.
The catalyst bed arrangement (simulating proportions of a typical refinery bed loading) which was used in the evaluation tests is shown in FIG. 1. The catalyst bed column had a diameter of about 0.75 inches. Particles A were substantially spherical alumina-containing particles, which can be any of the particles A1 through A12 described in more detail in Example II. Material B was a commercial alumina-supported hydrotreating catalyst comprising 0.9 weight-% Co, 0.5 weight-% Ni and 7.5 weight-% Mo, having a BET/N.sub.2 surface area of 174 m.sup.2 /g and a pore volume of 0.63 cc/g (measured by mercury intrusion porosimetry). Material C was a commercial alumina-based hydrotreating catalyst comprising 3.1 weight-% Ni, 7.9 weight-% Mo and 4.6 weight-% Ti having a BET/N surface area of 140 m.sup.2 /g and a pore volume (by Hg intrusion porosimetry) of 0.5 cc/g. Material D was a commercial alumina-based hydrotreating catalyst comprising 2.4 weight-% Co and 6.7 weight-% Mo, having a BET/N.sub.2 surface area of 290 m.sup.2 /g and pore volume (by Hg intrusion porosimetry) of 0.47 cc/g.
A heavy oil-water mixture containing about 4-8 volume-% H.sub.2 O was pumped to a metallic mixing T-pipe where it was mixed with a controlled amount of hydrogen gas. The heavy oil was a Maya 400F+ resid having an API.sup.60 gravity of 14.0, containing 3.8 weight-% sulfur and about 350 ppmw (Ni+V) (parts by weight of Ni+V per million parts by weight of oil feed). The oil/water/hydrogen mixture was pumped downward through a stainless steel trickle bed reactor which contained the multi-layer catalyst bed described above (see FIG. I). The tubular reactor was about 28.5 inches long, had an inner diameter of about 0.75 inches, and was fitted inside with a 0.25 inch O.D. axial thermocouple well. The reactor was heated by a 3-zone furnace. The reactor temperature was usually measured in four locations along the reactor bed by a traveling thermocouple that was moved within the axial thermocouple well.
Generally, the hydrotreating conditions were as follows: reaction temperature of about 690.degree.-720.degree. F.; liquid hourly space velocity (LHSV) of about 0.3 cc/cc catalyst/hour; about 2,250 psig total pressure; about 400 psig H.sub.2 O (steam) partial pressure; time on stream: about 100-200 hours. When it was desired to determine the desulfurization and demetallization activity of the catalyst bed, the liquid product was filtered through a glass filter and analyzed for sulfur, nickel and vanadium by plasma emission analysis.
After completion of a hydrotreating test, the reactor with catalyst bed was flushed with xylene so as to remove undrained oil. Thereafter, nitrogen gas was passed through the xylene-washed catalyst bed so as to dry it. The various catalyst layers were carefully removed. Particles A, B or C were tested for crush strength in a Mechanic Force Gauge D-75M of Hunter Spring, Division of Ametek, Hot Field, Pa. A single sphere of A or B or C, the average diameter of which had been measured, was placed between the metal plates of D-75M, and the plates were slowly moved toward one another by means of an electric motor. The force applied to the plates was displayed by a gauge. The force necessary to fracture (crush) a catalyst sphere was recorded as the crush strength of the sphere. The normalized crush strength, defined as crush strength of a sphere divided by its average particle diameter (lb/sphere/inch diameter), was calculated.
EXAMPLE V
This example illustrates the preparation of the substantially spherical alumina-containing particles of this invention and of other alumina-containing catalyst bed particles.
Control Particles A1 were spherical, Co/Mo-promoted alumina particles, marketed by Shell Chemical Company, Houston, Tex. under the product designation "Shell 544", suitable as support balls for hydrotreating catalyst beds. Pertinent properties of Particles A1 were: diameter of 1/6 inch; cobalt content of 1.7 weight-%; molybdenum content of 5.3 weight-%; surface area of 300+ m.sup.2 /g; total pore volume of 0.47 cc/g; loss on ignition (LOI; weight loss when heated to 482.degree. C.) of 0.8 weight-%; compacted bulk density (compacted loading density) of about 0.83 g/cc; and side plate crush strength of 30+ lb/particle (i.e., about 190 lb/particle/inch diameter).
Control Particles A2 were substantially spherical, substantially unpromoted alumina-containing particles having an average particle diameter of 1/4 inch; a BET/N.sub.2 surface area of about 325 m.sup.2 /g; a total pore volume of about 0.50 m.sup.2 /g; and average normalized individual ball crush strength of about 240 lb/particle/inch diameter (i.e., the actual crush strength of a 1/4" sphere was about 60 lb/particle); Al.sub.2 O.sub.3 content of about 94.6 weight-%; Na.sub.2 O content of about 0.35 weight-%; and LOI content (weight loss when heated from 250.degree. C. to 1200.degree. C.; a measure of hydroxyl content) of 5.0 weight-%. Particles A2 were supplied by Aluminum Company of America, Pittsburgh, Pa. under the product designation of S-100.
Control Particles A3 were obtained when Control Particles A2 were heated at about 650.degree. C. for about one hour.
Control Particles A4 were obtained by soaking 100 grams of Control Particles A2 with an aqueous solution containing about 1.1 grams of ammonium heptamolybdate, (NH.sub.4).sub.6 Mo.sub.7 O.sub.24.H.sub.2 O (provided by Alfa Products, Danvers, Mass.), dissolved in 100 cc of deionized water for about 20 minutes, as to provide a promoter level of about 0.3 weight-% Mo in the particles (after calcining); decanting excess solution; drying the thus impregnated particles at about 150.degree. C. for about 2 hours, and then calcining them at about 650.degree. C. for about 2 hours in air.
Control Particles A5 also contained about 0.3 weight-% Mo, and were obtained when 60 grams of Control Particles A2 were soaked in 100 cc of an aqueous solution containing about grams of ammonium heptamolybdate and about 3.0 grams of ammonium bisulfate, NH.sub.4 HSO.sub.4, decanting excess solution, drying at about 150.degree. C. for about 2 hours and calcining at about 650.degree. C. for about 2 hours in air.
Control Particles A6 were prepared essentially in accordance with the preparation of Particles A5, except that (NH.sub.4).sub.2 SO.sub.4 (3.0 grams) was used in lieu of NH.sub.4 HSO.sub.4.
Invention Particles A7 were prepared essentially in accordance with the preparation procedure for Particles A5, except that NH.sub.4 SCN (3.0 grams) was used in lieu of NH.sub.4 HSO.sub.4.
EXAMPLE VI
This example illustrates the effect of the impregnation of spherical alumina particles with various ammonium salts on the crush strength of the calcined particles.
In one test series, the average crush strength of Invention Particles A7 aas compared with the average crush strength of Control Particles A4, A5 and A6, measured in accordance with the procedure described in Example V. Test results are summarized in Table II.
TABLE II______________________________________ NH.sub.4 Salts in Wt % of NH.sub.4 Crush StrengthParticles Impregn. Solution Salt in Solution (Lb/Particle)______________________________________A4 None 0 8.2(Control)A5 NH.sub.4 HSO.sub.4 3.0 8.3(Control)A6 (NH.sub.4).sub.2 SO.sub.4 3.0 9.0(Control)A7 NH.sub.4 SCN 3.0 9.8(Invention)______________________________________
Test data in Table II clearly show the improvement in crush strength (after hydrotreating in the presence of steam) of Invention Particles A7 (pretreated with NH.sub.4 SCN versus Control Particles A5 and A6 (pretreated with NH.sub.4 HSO.sub.4 and (NH.sub.4).sub.2 SO.sub.4, respectively). Particles A4-7 all contained 0.3 weight-% Mo.
EXAMPLE VII
This example illustrates the effect of the heating (calcining) conditions on pertinent physical properties of alumina-containing spheres. A2 particles of about 1/8 inch diameter that had been impregnated with about 0.3 weight-% Mo were heated in air at temperatures ranging from 400.degree. C. to 900.degree. C. for about 1 hour (so as to prepare Particles A4). The crush strength of the thus calcined particles (diameter: 1/8 inch) was determined in accordance with the procedure described in Example IV. Tests results are summarized in Table III and are plotted in FIG. 2.
TABLE III______________________________________ Crush NormalizedCalcination Strength Crush StrengthTemp. (.degree.C.) (lb/Particle) (lb/Inch Diameter)______________________________________400 1.88 15.0500 3.42 27.4600 4.37 35.0700 4.80 38.4800 3.95 31.6900 1.65 13.2______________________________________
Data in Table III and FIG. 2 clearly show that maximum crush strength (after hydrotreating in the presence of steam) was attained when the alumina spheres (containing 0.3 weight-% Mo) were calcined at a temperature in the range of from about 550.degree. to about 800.degree. C., preferably from about 600.degree. to about 750.degree. C.
The effect of the calcination time, at a calcination temperature of 650.degree. C., is shown in Table IV.
TABLE IV______________________________________Calcination Crush Strength Crush StrengthTime (minutes) (lb/Particle) (lb/Inch Diameter)______________________________________20 7.01 56.140 7.25 58.060 7.20 57.690 6.68 53.4120 6.41 51.3240 5.22 41.8______________________________________
Data in Table IV show that a calcination time of about 20-90 minutes was suitable for 1/8 inch diameter alumina-containing Particles A4. Prolonged calcining had a detrimental effect.
Based on the above-described test results, it is concluded that the preferred heating conditions in step (A) for preparing the NH.sub.4 SCN-impregnated, substantially spherical alumina-containing particles of this invention (such as Particles A7) will also comprise a temperature of about 550.degree.-800.degree. C. (more preferably about 600.degree.-750.degree. C.) and a heating time of about 20-90 minutes.
EXAMPLE VIII
The effect of the calcination temperature of the pore volume distribution of Particles A1, A2 and A3 was investigated. Pore volume and pore diameter of these particles were determined by measuring intrusion porosimetry (carried out at room temperature at a mercury ranging from 0 psi to 60,000 psi, using an Autopore 9200 instrument of Micromeritics, Norcross, Ga.). In FIG. 3. pore volume was plotted versus logarithm of pore diameter for A1, A2 and two A3 samples. FIG. 4 shows that A1 (Shell 544, as received; 1/6" diameter) and of A2 (Alcoa S-100, as received; 1/16" diameter) had very similar pore distributions, whereas the pore distributions of the two A3 samples (obtained by heating 1/16" A2 particles at 600.degree. C. and 800.degree. C., respectively, for about 3 hours), differed significantly from those of A1 and A2. The most significant changes that resulted when A2 (S-100) particles were heated to 600.degree. C. and 800.degree. C., respectively, (so as to make A3 particles), was a shift toward a substantially greater portion of pores in the 40-200A pore diameter range. About 80% of the total pore volume of A3 was in pores of the 40-200 Angstrom range, whereas the percentage of the total pore volume of A1 and A2 in the 40-200 Angstrom pore diameter range was only about 40%.
Based on the above-described test results, it is concluded that heating at 600-800.degree. C. in step (A) for preparing the NH.sub.4 SCN-impregnated, substantially spherical alumina-containing particles of this invention will have a very similar effect in the pore volume distribution of the particles of this invention (such as Particles A7) as the above-described effect on the pore volume distribution of Particles A3.
The total pore volume of the Mo-impregnated alumina spheres A3 ranged from about 0.5 to about 0.6 cc/g when the calcination was carried out for 16 hours at a temperature in the range of from about 400.degree. C. to about 800.degree. C. Thus, the effect of the calcination temperature on the total pore volume of calcined spheres A3 was rather insignificant. Based on these results, it is concluded that the total pore volume of the NH.sub.4 SCN-impregnated, substantially spherical alumina-containing particles of this invention (such as Particles A7) will also vary only insignificantly with the calcination temperature.
EXAMPLE IX
This example illustrates the improved performance of Particles A4 (with 0.3 weight-% Mo) in prolonged hydrotreating tests versus Particles A1 and A2. Crush strength results, obtained substantially in accordance with the hydrotreating procedure described in Example I, are summarized in Table V. Hydrotreating conditions were: 2200 psig total pressure; 760.degree. F.; 110 psi steam pressure, LHSV of 0.1 cc/cc catalyst/hour. The resid feed contained about 2.0 weight-% sulfur and about 60 ppmw (Ni+V).
TABLE V______________________________________Hours on Stream:0 16 30 140 270 360Particles.sup.1 Crush Strength (lb/Particle)______________________________________1/6" A1 35 11 N/A N/A N/A N/A1/4" A2 58 11 N/A N/A N/A N/A1/4" A4 55 39 37 34 38 381/4" A4 100+ 80+ 80+ 80+ 80+ 80+1/8" B 49 N/A 42 N/A N/A N/A______________________________________ .sup.1 Fractions indicate particle diameter expressed in inches.
Test data in Table V clearly show a significant improvement in crush strength retention of Particles A4 over commercial Particles A1 and A2, after use in the several hydrotreating runs in the presence of steam, as described in Example V. Based on these results and based on the fact that the NH.sub.4 SCN-impregnated, substantially spherical alumina-containing Particles A7 of this invention have a higher crush strength retention than Particles A4 (see Table III), it is concluded that the NH.sub.4 SCN-impregnated, substantially spherical alumina-containing particles of this invention will also be superior to Particles A1 and A2, in terms of crush strength retention.
Reasonable variations and modifications are possible within the scope of the disclosure and appended claims.

Claims

1. A hydrotreating process comprising the step of contacting a substantially liquid hydrocarbon-containing feed stream, which also contains compounds of at least one metal and/or sulfur as impurities, with a free hydrogen containing gas and a catalyst composition, under such conditions as to produce a hydrocarbon-containing stream having reduced levels of said at least one metal and sulfur;
wherein said catalyst composition has been prepared by a process comprising the steps of
(A) impregnating a support material comprising alumina with a solution consisting essentially of water and at least one dissolved thiocyanate compound;
(B) heating the material obtained in step (A) under such conditions as to at least partially dry said material obtained in step (A);
(C) impregnating the at least partially dried material obtained in step (B) with a solution comprising a liquid solvent and at least one dissolved compound of at least one metal selected from the group consisting of transition metals belonging to Group VB, VIB, Group VIIB, Group VIII and Group IB of the Periodic Table of Elements;
(D) heating the material obtained in step (C) at a first temperature so as to at least partially dry said material obtained in step (C); and
(E) heating the at least partially dried material obtained in step (D) at a second temperature, which is higher than said first temperature, so as to activate said at least partially dried material obtained in step (D).
2. A hydrotreating process in accordance with claim 1 wherein said thiocyanate compound used in step (A) is NH.sub.4 SCN.
3. A hydrotreating process in accordance with claim 2 wherein the concentration of NH.sub.4 SCN in the solution used in step (A) is in the range of from about 1 to about 200 g grams per liter.
4. A hydrotreating process in accordance with claim 3 wherein the weight ratio of said support material to said solution used in step (A) is in the range of from about 1:20 to about 5:1.
5. A hydrotreating process in accordance with claim 1 wherein said support material used in step (A) has a surface area, determined in accordance with ASTm method D3037, of about 20 to about 350 m.sup.2 g, and a pore volume, measured by mercury intrusion porosimetry, of about 0.2 to about 2.0 cc/g.
6. A hydrotreating process in accordance with claim 5 wherein said support material consists essentially of alumina.
7. A hydrotreating process in accordance with claim 1 wherein heating steps (B) and (D) are carried out at a temperature of about 40.degree. to about 300.degree. C., and heating step (E) is carried out at a temperature of about 300.degree. C. to about 700.degree. C.
8. A hydrotreating process in accordance with claim 1 wherein said liquid solvent of the solution used in step (C) is water the concentration of said at least one dissolved compound of at least on metal is in the range of from about 0.01 to about 5.0 mol/l, and the weight ratio of said at least partially dried material obtained in step (B) to said solution used in step (C) is in the range of from about 1:100 to about 10:1.
9. A hydrotreating process in accordance with claim 1 wherein said at least one metal in said at least one dissolved compound used in step (C) is selected from the group consisting of Mo, Ni and Co, and the weight percentage of said at least one metal in the activated material obtained in step (E) is in the range of from about 0.1 to about 25 weight-%.
10. A hydrotreating process in accordance with claim 1 wherein said process for preparing said catalyst composition further comprises the step of
(F) contacting the activated material obtained in step (D) with at least one suitable sulfur containing compound under such conditions as to at least partially convert transition metal compounds contained in said activated material to transition metal sulfides.
11. A hydrotreating process in accordance with claim 1 wherein said substantially liquid hydrocarbon-containing feed stream comprises about 3-500 ppmw Ni, about 5-1000 ppmw V and about 0.3-5 weight-% S.
12. A hydrotreating process in accordance with claim 1 wherein said hydrotreating conditions comprise a reaction temperature in the range of from about 250.degree. C. to about 550.degree. C., a reaction pressure in the range of from about 0 to 5,000 psig, a reaction time in the range of from about 0.05 to about 10 hours, and an amount of added hydrogen gas in the range of from about 100 to about 10,000 standard cubic feet H.sub.2 per barrel of hydrocarbon-containing feed stream.
13. A hydrotreating process in accordance with claim 12 wherein said hydrotreating conditions comprise a reaction temperature in the range of from about 350.degree. C. to about 450.degree. C., a reaction pressure in the range of from about 100 to about 2,500 psig, a reaction time in the range of from about 0.4 to about 5 hours, and an amount of added hydrogen as in the range of from about 1,000 to about 6,000 standard cubic feet H.sub.2 per barrel of hydrocarbon-containing feed stream.
14. A hydrotreating process in accordance with claim 13 wherein to said hydrocarbon-containing feed stream has been added at least one thermally decomposable compound of a metal selected from the group consisting of metals belonging to Groups IB, IVB, VB, VIB, VIIB and VIII of the Periodic Table of Elements.
15. A hydrotreating process in accordance with claim 14 wherein the at least one added thermally decomposable metal compound is a molybdenum compound and the added molybdenum content in the hydrocarbon-containing feed stream is about 1-1000 ppmw Mo.
16. A hydrotreating process comprising the step of contacting a substantially liquid hydrocarbon-containing feed stream, which also contains compounds of at least one metal and/or sulfur as impurities, with a free hydrogen containing gas in the presence of a fixed catalyst bed comprising at least one layer (X) of impregnated, substantially spherical alumina-containing particles, under such hydrotreating conditions as to obtain at least one liquid hydrocarbon-containing product stream having lower concentrations of sulfur and said at least one metal than said hydrocarbon-containing feed stream;
wherein said impregnated, substantially spherical alumina-containing particles in fixed catalyst bed layer (X) have been prepared by a process comprising the steps of
(a) impregnating (i) a starting material of substantially spherical alumina-containing particles which have an initial average particle diameter of at least about 0.05 inch, an initial BET/N.sub.2 surface area of at least 20 m.sup.2 g, an initial Hg intrusion pore volume of at least about 0.1 cc/g, and an initial content of Al.sub.2 O.sub.3 of at least about 80 weight-%, with (ii) a solution comprising dissolved ammonium thiocyanate; and
(b) heating the material obtained in step (a) at a temperature in the range of from about 500.degree. to about 900.degree. C. for a period of time of at least 10 minutes, under such heating conditions as to obtain a material having a higher crush strength than said starting material, wherein the crush strength is measured after exposure of each of said materials for about 100 hours to a liquid hydrocarbon-containing stream which contains at least about 0.5 weight-% sulfur, under hydrotreating conditions at about 2250 psig total pressure, about 400 psig partial pressure of steam and about 700.degree. F.
17. A hydrotreating process in accordance with claim 16 wherein said starting material used in step (a) has an initial average particle size in the range of from about 0.1 to about 1.0 inch, an initial surface area in the range of from about 40 to about 600 m.sup.2 /g, an initial pore volume in the range of from about 0.2 to about 1.0 cc/g, and an initial normalized crush strength in the range of from about 100 to about 400 lb. per inch diameter per particle.
18. A hydrotreating process in accordance with claim 16 wherein said initial content of Na is below about 2.0 weight-%, and said initial content of Al.sub.2 O.sub.3 is in the range of from about 90 to about 99 weight-%.
19. A hydrotreating process in accordance with claim 16 wherein the concentration of dissolved ammonium thiocyanate in the impregnating solution used in step (A) is in the range of from about 0.05 to about 5 mol/l and the weight ratio of said starting material to said impregnating solution is in the range of from about 0.1:1 to about 2.0:1.
20. A hydrotreating process in accordance with claim 19 wherein said concentration of dissolved ammonium thiocyanate is inthe range of from about 0.1 to about 1.0 mol/l.
21. A hydrotreating process in accordance with claim 16 wherein said heating in step (b) is carried out at a temperature in the range of from about 550.degree. to about 800.degree. C. for a period of time in the range of from about 10 minutes to about 20 hours.
22. A hydrotreating process in accordance with claim 16 wherein said impregnated, substantially spherical alumina-containing particles obtained in step (b) have a pore volume of pores possessing a diameter of about 40-200 Angstroms in the range of from 50% to about 90% of the total pore volume, and a crush strength in the range of from about 150 to about 350 lb. per inch diameter per particle.
23. A hydrotreating process in accordance with claim 16 wherein said impregnated, substantially spherical alumina-containing particles obtained in step (b) have a surface area in the range of from about 50 to about 300 m.sup.2 /g and a pore volume in the range of from about 0.3 to about 0.8 cc/g.
24. A hydrotreating process in accordance with claim 16 wherein said impregnated spherical alumina-containing particles have been promoted with at least one element or compound of at least one element selected from the group consisting of Y, La, Ce, Ti, Zr, Hf, Cr, Mo, W, Mn, Re, Ni, Co, Cu, Zn and P.
25. A hydrotreating process in accordance with claim 24 wherein said at least one element is selected from the group consisting of Mo, Ni and Co.
26. A hydrotreating process in accordance with claim 24 wherein said at least one element is present at a level of from about 0.1 to about 2.0 weight-%.
27. A hydrotreating process in accordance with claim 16 wherein said catalyst bed further comprises at least one layer (Y) of catalyst particles comprising a refractory inorganic carrier and said at least one hydrogenation promoter selected from the group consisting of transition metals belonging to Groups IIIB, IVB, VB, VIB, VIIB, VIII, IB and IIB of the Periodic Table and compounds of said transition metals.
28. A hydrotreating process in accordance with claim 27 wherein said refractory inorganic carrier comprises alumina, and said at least one hydrogenation promoter is selected from the group consisting of compounds of Y, La, Ce, Ti, Zr, Cr, Mo, W, Mn, Re, Ni, Co and Cu.
29. A hydrotreating process in accordance with claim 22 wherein said catalyst particles in layer (Y) comprise alumina as carrier material and at least one hydrogenation promoter selected from the group consisting of oxides and sulfides of Mo, oxides and sulfides of Ni, oxides and sulfides of Co, and mixtures thereof, and have a surface area in the range of from about 50 to about 500 m.sup.2 /g, a pore volume in the range of from about 0.2 to about 2.0 cc/g.
30. A hydrotreating process in accordance with claim 27 wherein layer (X) of impregnated, substantially spherical alumina-containing particles is placed below at least one layer (Y) of catalyst particles.
31. A hydrotreating process in accordance with claim 27 wherein layer (X) of impregnated, substantially spherical alumina-containing particles is placed on top of at least one layer (Y) of catalyst particles.
32. A hydrotreating process in accordance with claim 27 wherein the weight ratio of each layer (X) of impregnated, substantially spherical alumina-containing particles to each layer (Y) of catalyst particles is in the range of from about 1:100 to about 1:1.
33. A hydrotreating process in accordance with claim 16 wherein said fixed catalyst bed has been contacted with at least one suitable sulfur containing compound under such conditions as to at least partially convert transition metal compounds contained in said fixed catalyst bed to transition metal sulfides.
34. A hydrotreating process in accordance with claim 16 wherein said substantially liquid hydrocarbon-containing feed stream comprises about 3-500 ppmw Ni, about 5-1000 ppmw V about 0.3-5 weight-% S.
35. A hydrotreating process in accordance with claim 16 wherein said hydrotreating conditions comprise a reaction temperature in the range of from about 250.degree. C. to about 550.degree. C., a reaction pressure in the range of from about 0 to 5,000 psig, a reaction time in the range of from about 0.05 to about 10 hours, and an amount of added hydrogen gas in the range of from about 100 to about 10,000 standard cubic feet H.sub.2 per barrel of hydrocarbon-containing feed stream.
36. A hydrotreating process in accordance with claim 16 wherein said hydrotreating conditions comprise a reaction temperature in the range of from about 350.degree. C. to about 450.degree. C., a reaction pressure in the range of from about 100 to about 2,500 psig, a reaction time in the range of from about 0.4 to about 5 hours, and an amount of added hydrogen gas in the range of from about 1,000 to about 6,000 standard cubic feet H.sub.2 per barrel of hydrocarbon-containing feed stream.
37. A hydrotreating process in accordance with claim 16 wherein to said hydrocarbon-containing feed stream has been added at least one thermally decomposable compound of a metal selected from the group consisting of metals belonging to Groups IB, IVB, VB, VIB, VIIB and VIII of the Periodic Table of Elements.
38. A hydrotreating process in accordance with claim 37 wherein said at least one added thermally decomposable metal compound is a molybdenum compound and the added molybdenum content in the hydrocarbon-containing feed stream is about 1-1000 ppmw Mo.
39. A hydrotreating process in accordance with claim 16 wherein water is present during said contacting under said hydrotreating conditions.
40. A hydrotreating process in accordance with claim 39 wherein said water is introduced in admixture with said hydrocarbon containing feed stream.
41. A hydrotreating process in accordance with claim 39 wherein said water is present as steam.

US Referenced Citations (13)

Number	Name	Date
3042197	Binning et al.	Jul 1962
3725531	Pearson et al.	Apr 1973
3926780	Ward	Dec 1975
4009125	Geierhaas et al.	Feb 1977
4048060	Riley	Sep 1977
4177136	Herrington et al.	Dec 1979
4212729	Hensley, Jr. et al.	Jul 1980
4320030	Happel et al.	Mar 1982
4374020	Trevino et al.	Feb 1984
4411771	Baumbrick et al.	Oct 1983
4431525	Hensley, Jr. et al.	Feb 1984
4491639	Huppel et al.	Jan 1985
4568664	Goodboy	Feb 1986

Non-Patent Literature Citations (3)

Entry
"Product Data S-100 Activated Alumina for Claus Catalysis", Alcoa Chemicals Division, 1984.
Technical Bulletins SC:175-80 and SC:462-80, Shell Chemical Company, 1980.
"Technical Data Actispheres: Protection Upper Layer", Procatalyse, 1985.

Hydrotreating process employing a pretreated alumina containing material

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

US Referenced Citations (13)

Non-Patent Literature Citations (3)