Patent Application
20050250642
1. Field of the Invention
The invention pertains to a continuous process and related apparatus for the conversion of inorganic solid starting particles which either are amorphous or possess a degree of order into solid inorganic product particles which when the starting particles are amorphous, possess a degree of order, or when the starting particles possess a degree of order, possess a different order, a different degree of order, or no order.
2. Prior art
Processes for the conversion of inorganic solid particles in the form of a suspension are known, for instance from German patent publication DE 38 23 895, which describes a process for the preparation of boehmite and alpha-aluminum oxide monohydrate compounds having variable pore radii in the range of 3 to 100 nm. In the said process suspensions containing 5 to 15 wt % Al2O3 are aged in an autoclave at a steam pressure of 1 to 30 bar, preferably for between 0.5 and 20 hours, whilst stirring at a peripheral speed of 1.0 to 6.0 m/s. The said stirring preferably takes place in a cascade reactor with 2 to 10, preferably 4 to 10 stages (as shown in FIG. 3 of DE 38 23 895).
The Solids to Liquid Ratio (SLR) in the process according to DE 38 23 895 ranges from roughly 0.05 to 0.18, which means that the suspensions used in this process are relatively large in volume and require similarly large reactors and peripheral equipment.
For many applications, e.g., catalysts, carriers, adsorbents, fillers, electronic materials and/or nano-technology applications, it is preferred to convert solid inorganic starting particles which either are amorphous or possess a degree of order into inorganic solid product particles which possess a degree of order, a different order, a different degree of order, or no order. In this specification “a degree of order” is defined as the presence of a crystalline or quasi-crystalline, i.e. non-amorphous, phase detectable by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) or extended X-ray adsorption fine structure (EXAFS). Normally, a degree of order will be X-ray detectable (either as a peak or as a lump), but in the case of very small crystallites (i.e. below the XRD detection limit) more advanced techniques are required to detect a degree of order: SEM, TEM, or EXAFS. On the other hand, amorphous is defined as not having a degree of order as defined above. The degree of order can be estimated for instance from the width of the XRD-peak (or lump) if the crystallites are X-ray detectable. The narrower this peak, the higher the degree of order. A different order will follow from the detection of different crystal structures or morphologies as detected by the techniques mentioned above. No order means amorphous.
In order to minimize the costs of operation and to maximise energy conservation, the conversion of inorganic solid starting particles is preferably carried out in a continuous mode and with the minimum of liquid required to suspend the starting particles on the one hand and ensure proper flow characteristics on the other.
Suspensions consist of a continuous phase, i.e. a liquid, and a dispersed phase, i.e. solid particles. Suspensions can be homogeneous or heterogeneous. In this specification, homogeneous suspensions are defined as suspensions having a constant volume fraction of the continuous phase throughout the whole system. Suspensions without such a constant volume fraction of the continuous phase are referred to as heterogeneous. In these heterogeneous systems there are concentration gradients of the dispersed phase.
Suspensions can separate into a fraction with a higher volume fraction of the continuous phase and a fraction with a lower volume fraction of the continuous phase. Within this specification this phenomenon is referred to as segregation. Segregation can occur by the action of various forces, for instance centrifugal forces or gravity. Sedimentation is a form of segregation where the dispersed phase settles by gravity.
When sediment is formed, part of the flow region within a reactor is blocked by a stagnant solid, reducing the volume available for free flow. With constant mass flux, the suspension will have to move through a smaller area, resulting in higher velocities of the continuous phase. This results in even more segregation and a non-ideal residence time distribution of the dispersed phase in the reactor.
The conversion of inorganic solid starting particles in a suspension may be performed continuously in traditional pipe reactors or cascade reactors as described for instance in the aforementioned DE 38 23 895, provided that the starting particles easily form a stable homogeneous suspension, e.g., a sol or a gel, and are of a more or less uniform particle size. Even then limitations in the Solids to Liquid Ratio (SLR) may occur due to the rheological behaviour of the homogeneous suspension. High-energy input, e.g., high-shear mixing, may alleviate these difficulties if the suspensions exhibit shear-thinning behaviour.
Unfortunately, many industrially interesting materials are not easily suspendable and/or do not form stable homogeneous suspensions at high solids to liquid ratios. This is due either to their large particle size (say >0.1 micron) or to their chemical incompatibility with the liquid, making segregation of the particles from the liquid very likely. This means that the solid particles will show a tendency to form a sediment layer, resulting in an uncontrolled and non-ideal residence time distribution in the reactor. This lack of homogeneity may hinder the conversion, especially when additional components, for instance colloidal seeds or other reactants, need to be contacted with the starting particles. This situation may be further aggravated if we are dealing with starting particles of different sizes.
Contrary to the case of the stable homogeneous suspensions described above, where high shear can assist in homogenisation and reduction of the viscosity, unstable suspensions tend to segregate even faster when a high-energy input is added to the system. Therefore, good mixing throughout the whole reactor and avoiding any dead or non-mixing zones is preferred to avoid non-ideal residence time distributions and to promote efficient conversion of the starting particles.
Alternatively, expensive chemicals need to be added in order to stabilize and disperse the suspension and to prevent segregation.
It is an object of the present invention to enable the conversion of suspended inorganic solid starting particles, such as (raw) ore and/or mineral particles, into suspended inorganic solid product particles suitable for use in or as a catalyst, in or as a carrier, or in or as an adsorbent.
In one embodiment, the present invention is a continuous process for the conversion of inorganic solid starting particles which either are amorphous or possess a degree of order into inorganic solid product particles which: When the starting particles are amorphous, possess a degree of order, or when the starting particles possess a degree of order, possess a different order, a different degree of order, or no order, which product particles are suitable for use in or as a catalyst, in or as a carrier, or in or as an adsorbent. In the process the starting particles are dispersed in a liquid thus forming a suspension. The suspension flows through at least two separate conversion vessels, which are connected in series, the suspension being agitated in each of these vessels. The conversion vessels are decoupled by one or more of the process conditions in one or more of the conversion vessels differing from those in the other vessel or vessels.
The invention further pertains to an apparatus for the conversion of inorganic solid starting particles employing decoupled conversion vessels as set forth above, including a first vessel for dispersing the starting particles in a liquid so as to form a suspension.
With the process of the present invention, it is possible to process suspensions with high Solids to Liquid Ratios (SLR) in a continuous mode, thereby enabling the use of relatively compact equipment and offering low costs of operation and energy consumption.
It was found that, as a result of agitation and the use of a series of separate vessels, suspensions having a high Solids to Liquid Ratio (SLR) can be processed without an unacceptable level of segregation of the solid particles.
Preferably, the suspension flows substantially upward through the said vessels and/or the mixer exerts mainly axial forces on the suspension, such that the whole reactor is well mixed and dead zones are avoided. With these measures, segregation of the solid particles and the liquid can be further suppressed and the solids to liquid ratio can be further increased. Also, an inhomogeneous distribution in the suspension of smaller particles on the one hand and larger particles on the other is substantially avoided.
A further advantage of the present invention resides in the possibility of fine-tuning particular (aspects of) process steps. It is thus preferred that at least one particular property of the product particles is controlled and/or amplified by adapting, preferably optimizing, the process conditions in at least one of the vessels. Within the framework of the present invention, this technique or procedure is called “de-coupling.” Hence, de-coupling means that in the series of conversion vessels the process conditions in one or more of the vessels differ from those in the other vessel or vessels.
This de-coupling of process stages can be used for, inter alia, effective control of the structure of the product particles. The advantage of de-coupling is not trivial: by de-coupling the various process steps it becomes possible for instance to optimize the mixing and handling of the solid-liquid suspension which can change in rheological behaviour during its conversion. Thus segregation, in the form of either sedimentation or separation of solids with different particle sizes, can be avoided even at high SLR.
De-coupling allows for optimization of the conditions of multi-stage processes. A separate, and important side effect can be the formation of a supersaturated solution. As solid-solid conversions are facilitated by the solvent, formation of a supersaturated solution will yield different product properties than a similar process without this occurrence. Supersaturation can be induced by cooling, removal of the solvent (evaporation) or addition of chemical agents that will lead to precipitation. The supersaturation can increase until the critical concentration, where nucleation is extremely fast.
For example, if one vessel is operated at a certain temperature, and the next vessel in the cascade exhibits a temperature 50° C. below that temperature, the feed entering this vessel may be supersaturated. Temperature differences between the various vessels can be substantial, up to about 50° C. per vessel. The amount of supersaturation (and the temperature difference between successive vessels) is dependant on the residence time (or the ratio between the holdup in the vessel and the feed). The inducement of superaturation need not need to be limited to one technique (temperature or chemical agent for example) only. Its application may be applied once or several times in the cascade, and be applied using one or various techniques, or combinations thereof.
By decoupling the temperature between vessels, each vessel may have a different temperature, with a corresponding autogenous pressure. Pressure differences between vessels will cause a flow from a high pressure vessel to a low pressure vessel if precautions are not taken. By applying a higher overall pressure (and no pressure difference between the vessels) this effect may be prevented.
Carrying out the process at autogenous pressure will require pressure control for each vessel. To facilitate the process, preferably the pressure is the same and constant and in all vessels, and slightly above the highest autogenous pressure occurring in one vessel of the process. Typically, the process will be carried out at 0.05 to 25 bar above the highest autogenous pressure occurring in the process, more preferably 0.5 to 10 bar above the highest autogenous pressure, most preferred 0.5 to 5 bar above the highest autogenous pressure.
Another possibility is the temporal suppression of crystal growth by adding a viscosity enhancing agent. In this case the ratio between crystal growth and nucleation of seeds can be modified. In a latter stage this viscosity enhancing agent can be removed or neutralized. Also in one stage an agent interfering with the crystallization can be added with the aim to change the crystal size distribution.
Another possibility that may be obtained by decoupling is stabilization of a seeding material. In this case, in a first stage at moderate temperature the seeds are subjected to mild aging, before they are exposed to high temperatures. In this case seeding will be more effective.
Application of all or some of the techniques described above give the possibilities to tailor the crystal size distribution. An example can be staged addition of seeds, yielding bi- or multimodal crystal size distributions.
The crystallization can go through gel formation and other known phases. The crystallites can grow to form large crystals or may remain small, even X-ray amorphous. The crystal- and agglomeration growth will determine the processability of the material; for example its Theological and filtration properties.
The apparatus according to the present invention is characterized by at least two, preferably three to five, separate and substantially vertical vessels which are connected in series and which each comprise a dedicated means for agitating the suspension. Axial or coaxial mixers are preferred.
The invention can be used for the conversion of (low-cost) inorganic solid starting particles, comprising for instance aluminum oxides or hydroxides, such as bauxite, crystalline aluminum trihydrate (ATH), gibbsite, bauxite ore concentrate (BOC) or thermally treated forms thereof, such as calcined and/or flash-calcined forms; synthetic and natural clays, such as kaolin, sepiolite, hydrotalcite or bentonite; silica ores, such as sand or diatomaceous earth; magnesium sources, such as magnesium salts, magnesium oxides or hydroxides, e.g., brucite, magnesium carbonate, magnesium hydroxy carbonate; zirconium compounds, such as zirconia, zircon or baddeleyite; titanium oxides or hydroxides; sorbents, catalysts or catalyst precursors, for instance in the form of microspheres, i.e. spray-dried particles, etc. The starting particles can first be reduced in size by mechanical milling, grinding, ultrasound treatment or chemical treatment with organic or inorganic acids or bases, such as nitric acid, sulfuric acid, acetic acid, formic acid, oxalic acid or caustic. Furthermore, improvements in conversion and process operations may be achieved if these starting particles are pre-treated in a high-energy deformation step, for instance milling, grinding, extrusion, flash calcination, flash freezing, ultrasound treatment, and microwaving. Such treatments can damage the particles, e.g., roughen their surface. It is even possible to use spent catalyst, ground brick, cement particles, ground stone or harbor sludge as starting particles.
When the starting particles are amorphous, the product particles possess a degree of order; when the starting particles possess a degree of order, the product particles possess a different order, a different degree of order, or no order at all. An example of the conversion of amorphous starting particles into product particles with a degree of order is the conversion of a precipitated mixture of aluminum sulfate and aluminum nitrate into boehmite. Examples of the conversion of starting particles with a degree of order into product particles with a different order, a different degree of order or no order are, respectively, the conversion of bauxite ore concentrate (BOC) into boehmite, the conversion of quasi-crystalline boehmite into micro-crystalline boehmite, and the conversion of aluminum trihydrate (ATH) with sodium silicate into an amorphous Si—Al cogel.
The conversion of the starting particles is conducted in the minimum of liquid required to suspend the materials on the one hand and to ensure proper flow characteristics on the other. Suitable liquids are for instance water, alcohols such as methanol, ethanol, n-propanol, isopropanol, etc., and hydrocarbon liquids such as toluene, hexane, white spirits, gasoline, etc. The liquid may contain dissolved material, such as sodium silicate, sodium aluminate, aluminum chloride, aluminum sulfate, vanadium compounds, phosphates and/or other metal salts.
Preferred products of the present process include shaped particles suitable as or for use in Fluidized Catalytic Cracking (FCC) catalysts, Hydro Processing Catalysts (HPC), Automotive Exhaust Catalysts or sorbents, comprising or essentially consisting of product particles obtained with the process according to the present invention.
Optionally, the process stages can be de-coupled by feeding additional ingredients (solvents, reactants, seeds or steam for heating purposes) to one or more of the conversion vessels by appropriate means such as injectors. For instance, a portion of the seeds can be fed to the second conversion vessel 3B via injector 6B. In this way it is possible to control the crystallite size and to obtain product particles with a small crystallite size instead of a large crystallite size.
Another way of de-coupling is changing the liquid during the process. This can be done by leading the suspension stream through a high-pressure solid-liquid separator (e.g. a centrifuge or high pressure filter) in between two conversion vessels, in which process the first liquid is removed and the remaining solid particles are mixed with a second liquid, and then leading the resulting mixture to the next conversion vessel, all in a continuous fashion.
It is also possible to provide one or more conversion vessels with an electrical transducer in order to introduce ultrasound waves into the suspension. This type of high energy can speed up the reaction. Another way to introduce high energy into the suspension is microwave treatment.
Suitable temperatures for the conversion of starting particles by the process according to the invention range from 20° to 300° C., preferably 50°-200° C., and even more preferably 10°-200° C. Depending on the liquid, the pressure resulting from the said temperatures may range from 1 to several tens of bars. If the liquid is water, a typical pressure would be roughly 10 bars at 170° C.
After conversion, the suspension containing the product particles (for instance boehmite with a particle size of 3-4 microns) leaves the last conversion vessel, e.g., the fourth vessel 3D, and is led through a duct 7 to a cooler unit 8, where the product is cooled down to, say, below 100° C. A mill 9 may be used to grind these product particles to an average particle size, e.g., roughly 1 micron, after which the suspension is separated into a product fraction of, e.g., 90% and a corresponding seeds fraction (10%). The seeds fraction is ground to particles having an average size of 0.3 to 0.5 micron in a further mill 10, which is connected to a seeds buffer tank 11, which in turn is connected to either the feed preparation vessel 1 or any one of the conversion vessels 3A-3D. By way of example,
The Solids to Liquid Ratio (SLR) of the suspension is defined as the weight ratio of solids, including crystal water, to liquid in the suspension. The process according to the invention allows processing of suspensions having an SLR up to 1.33. The optimal SLR depends on the rheological behavior of the suspension, e.g. the tendency to form a gel. The viscosity of the suspension is preferably between 1 and 500 Pa·s at a shear rate of 0.1 s−1. For aluminum (hydr)oxide suspensions, the SLR is preferably in the range from 0.5 to 1.33, even more preferably in the range from 0.65 to 1.00. The preferred viscosity of aluminum (hydr)oxide suspensions is also between 1 and 500 Pa·s at a shear rate of 0.1 s−1.
The average residence time in the vessels, i.e. all vessels together, is preferably between 10 and 120 minutes.
If desired, the product particles formed in the present process may be shaped to form shaped bodies. Suitable shaping methods include spray-drying, pelletising, extrusion (optionally combined with kneading), beading, or any other conventional shaping method used in the catalyst and absorbent fields or combinations thereof. The amount of liquid present in the suspension used for shaping should be adapted to the specific shaping step to be conducted. It might be advisable to partially remove the liquid used in the suspension and/or add an additional or another liquid, and/or to change the pH of the precursor mixture to make the suspension gellable and thus suitable for shaping. Various additives commonly used in the different shaping methods, e.g. extrusion additives, may be added to the precursor mixture used for shaping.
With this process various materials can be produced starting from inexpensive (raw) materials. For instance, it is now possible to produce silica and silica-based materials from an inexpensive silicate ore such as sand. Prior art methods for the production of these materials use either sodium silicates (water glass), tetra-ethoxy silane (TEOS) or sol-gel methods. With the process according to the invention it is possible to produce homogeneous silicas and silica-based materials from sand at a high solids content, in a continuous mode, and with limited reaction times. The reaction comprises treating the silicate ore with acid in the first conversion vessel (3A), optionally ion-exchanging in the second conversion vessel (3B) by adding an effective amount of suitable ions, and aging in the third conversion vessel (3C). Moreover, part of the formed material may be recycled and used as a seed.
Another product which can easily be obtained by the process according to the invention is a layered magnesium silicate with a short range order, which can be prepared by high-temperature treatment, i.e. above 100° C., of a silica source (e.g., sand, silica sol, water glass, diatomaceous earth) and a magnesium source such as MgO, brucite, hydromagnesite or magnesium salts.
The process according to the invention is also suitable for the production of highly crystalline zirconia by recrystallization of zirconia ores (e.g. zircon or baddeleyite) and the production of zirconia-based solid super acids. These solid super acids can be obtained by recrystallization of zirconia ore via high-temperature treatment, i.e. above 100° C., in the first conversion vessel, followed by reaction with a sulfate- or phosphate-containing compound in the second conversion vessel.
The present process enables the production of gels. For instance, aluminum phosphate gels can be prepared by treating aluminum trihydrate, e.g., bauxite ore concentrate (BOC) or flash-calcined BOC, with phosphates such as H3PO4, (NH4)2HPO4, (NH4)H2PO4 or mixtures thereof in aqueous suspension. Likewise, Al-containing cogels, e.g., Al—Zr cogel, Al—Ti cogel or Al—Si cogel, can be prepared from BOC or flash-calcined BOC and a Zr, Ti, and Si source, respectively. Additionally, as will be explained below, it is possible to use such gels, e.g., Si—Al cogels, as intermediates in the production of other materials.
With the process according to the invention it is also possible to produce and stabilize zeolites and other silica-aluminas from inexpensive starting materials at a high-solids content, in a continuous mode, and with limited reaction times.
For instance, an aluminum source, e.g. aluminum trihydrate, thermally treated forms thereof, boehmite, aluminum chlorohydrol, or mixtures thereof, and an acidic silica source, e.g. sodium (meta)silicate, are converted in conversion vessel (3A) into a Si—Al cogel. In the second conversion vessel (3B) seeds, templates, and further reactants can be added to support the crystallization of the cogel into a zeolite, for instance zeolite X, Y, A, ZSM, beta or mesoporous molecular sieves, depending on the seeds used. Part of the resulting product can be milled and recycled as a seed.
Alternatively, silica can be prepared in the first conversion vessel 3A (for instance from silicate ore or sand), with the zeolite production and the stabilization being performed in conversion vessels 3B and 3C. It is of course also possible to produce alumina (for instance from BOC) in conversion vessel 3A, followed by zeolite production and stabilization in conversion vessels 3B and 3C.
With the present process it is also possible to crystallize zeolites in situ by using microspheres as starting particles. These microspheres may comprise, for instance, kaolin (e.g., hydrous kaolin and/or calcined kaolin), aluminum trihydrate, and a silica binder (e.g., silica sol). Crystallization of zeolites in these microspheres can be performed by the addition of seeds, caustic, and a silica source, e.g., sodium silicate, to one of the vessels.
The so-formed zeolites can be stabilized or activated by treatment at high temperature and pressure, for instance in water above 100° C. and at autogenous pressure. This treatment can be performed during preparation of the zeolite, i.e. in the second conversion vessel, or afterwards in the last conversion vessel. Alternatively, ion-exchange (with for instance rare earth metals, Mg, Ca, Fe, Mn, V, ammonium, etc.), de-alumination (with acid) or de-silication (with base) can be performed in subsequent conversion vessels, at temperatures either below or above 100° C. This shows once more the advantage of de-coupling.
Another possibility is the formation of boehmite from inexpensive aluminum sources like aluminum trihydrate or a thermally treated form thereof, for instance BOC or flash-calcined BOC, or microspheres comprising an aluminum source. The crystallinity of boehmite can be varied by de-coupling, for instance by varying the moment of addition of seeds, varying the pH by adding acids or bases, and/or varying the temperature in the different vessels.
For instance, adding part of the seeds in the second conversion vessel will give boehmite with lower crystallinity than adding all the seeds in the first conversion vessel. Analogously, comparable results can be achieved by the addition of crystal growth inhibitors, such as gluconic acid, sodium gluconate, sucrose, swellable clays, and hydroxides, phosphates, sulfates, and silicates of ammonium and alkali or alkaline earth metals, to the second conversion vessel.
Another way of changing the crystallinity, i.e. the degree of order, is by changing the temperature in the conversion vessels. Higher temperatures will result in more crystalline boehmites than lower temperatures. For instance, at temperatures above 100° C. micro-crystalline boehmite is formed, whereas at temperatures below 85° C. quasi-crystalline boehmite is formed. So, the ratio of micro-crystalline boehmite to quasi-crystalline boehmite can be varied by producing micro-crystalline boehmite at relatively high temperatures in the first conversion vessel and feeding an additional amount of aluminum source to the second conversion vessel, which is lower in temperature, resulting in the formation of quasi-crystalline boehmite.
A further method for changing the crystallinity is changing the pH: at a pH between 1 and 6 quasi-crystalline boehmite is formed, whereas at a higher pH micro-crystalline boehmite is formed.
Boehmite can also be prepared via aluminum chlorohydrol or aluminum nitrohydrol solutions. To this end, aluminum trihydrate, e.g., BOC, or its thermally treated form, e.g., flash-calcined BOC, is reacted in the first conversion vessel with hydrochloric acid or nitric acid to give, respectively, aluminum chlorohydrol and aluminum nitrohydrol. In the subsequent conversion vessels these solutions can be treated thermally or hydrothermally in the way described above in order to obtain a quasi-crystalline boehmite, a micro-crystalline boehmite or a mixture thereof.
The production of zeolite and the production of boehmite can be combined in the process according to the invention. For instance, in the first one to three conversion vessels micro-crystalline boehmite, quasi-crystalline boehmite or a mixture of both can be prepared from, e.g., BOC, flash-calcined BOC or microspheres comprising these aluminum sources. In subsequent conversion vessels a silica source, for instance sodium silicate or polysilicic acid, can be added, optionally together with zeolite seeds and caustic, to obtain a zeolite or a zeolite-containing composition. These zeolites can be ion-exchanged, ultrastabilized and/or de-aluminated in subsequent conversion vessels under hydrothermal conditions.
The process according to the invention is also very suitable for the preparation of anionic clay from inexpensive divalent and trivalent metal compounds. By anionic clays are meant hydrotalcite-like materials and layered double hydroxides, terms interchangeably used by those skilled in the art. Suitable divalent and trivalent metals are Mg and Al. Examples of Mg—Al anionic clays are hydrotalcite and meixnerite.
Suitable starting materials for the production of anionic clays by the process according to the invention are aluminum trihydrate, e.g., gibbsite or BOC, thermally treated forms thereof such as flash-calcined BOC, aluminum chlorohydrol, aluminum nitrohydrol, microspheres comprising aluminum trihydrate, kaolin, boehmite, and/or amorphous alumina, and magnesium oxide or hydroxide. De-coupling, i.e. varying the process conditions in the different conversion vessels, offers the possibility of varying the ratio of different anionic clay polytypes. For instance, in the first conversion vessel 3R2 anionic clay can be formed, while in the second conversion vessel carbonate can be added to this 3R2-type clay, forming a 3R1-type anionic clay.
Another option offered by this process is the formation of boehmite in the first conversion vessel and the formation of anionic clay in any of the following conversion vessels by the addition of a magnesium source, all in a continuous mode.
Optionally, a silica source may be added to one of the vessels, resulting in the formation of smectites or saponites.
Another method for preparing anionic clays involves the addition of a solid solution to the feed preparation vessel, followed by hydrothermal rehydration of the solid solution in the at least two conversion vessels to form an anionic clay. The anionic clays can be subjected to ion-exchange in one of the conversion vessels of the apparatus by introducing an anion-bearing salt into that vessel. Examples of suitable anions are carbonate, bicarbonate, nitrate, chloride, sulfate, bisulfate, vanadates, tungstates, borates, phosphates, and pillaring anions such as V2O74−, HV2O124−, V3O93−V10O286−, Mo7O246−, PW12O403−, B(OH)4−, B4O5(OH)42−, [B3O3(OH)4]−, [B3O3(OH)5]2− HBO42−, HGaO32−, CrO42−, Keggin-ions, formate, acetate, and mixtures thereof.
In all these processes, additives may be added to any of the vessels to obtain doped materials, e.g., doped silica, doped boehmite, doped zeolites, doped magnesium silicates, doped anionic clays, and combinations thereof. Suitable additives are compounds containing elements selected from alkaline earth metals (for instance Ca and Ba), alkaline metals, transition metals (for example Mn, Fe, Ti, Zr, Cu, Ni, Zn, Mo, W, V, Sn), actinides, rare earth metals such as La, Ce, Nd, noble metals such as Pt and Pd, silicon, gallium, boron, and phosphorus.
All sorts of combinations of the above procedures can be used to form various composites, for instance anionic clay and boehmite-containing composites, or composites comprising anionic clay, boehmite, and zeolite. Such compositions can be prepared by adding the different starting materials as starting particles to the vessels, but also by using shaped bodies, e.g. microspheres, comprising the starting materials as the starting particles. By hydrothermally treating these shaped bodies, shaped bodies comprising the above-compositions can be obtained in situ. The advantage of such a process is that no shaping step is required after the hydrothermal treatment.
Moreover, this process can be used for the rejuvenation or activation of spent catalysts, such as FCC equilibrium catalysts.
The invention is further illustrated by the following Examples.
The mixing behavior within a conversion vessel of the apparatus according to the present invention was studied by determination of the residence time distribution curve. If segregation occurs or non-mixing zones are present in the vessel, the distribution will deviate substantially from the theoretical residence time distribution of an ideally mixed reactor (CSTR).
Before the experiment started, the vessel, with a volume of 500 litres and agitated using a double-helix impeller at 76-83 rpm, was filled with a highly viscous shear-thinning alumina suspension (upflow). Subsequently, a suspension of BOC and boehmite seeds (Condea® P-200) with a solids to liquid ratio of 0.72 was pumped through the reactor with a flow rate of 48.3 l/min. The replacement of the shear-thinning alumina by BOC was measured by determining the particle size distribution of the suspension coming out of the reactor.
The result of this experiment is shown in
Comparison
Reference Example A was repeated, except that a pipe reactor with internal packings, viz. a Sulzer® pipe reactor, was used. Ideally, a pipe reactor should show a step change in BOC concentration (plug flow), which means that the BOC concentration of the suspension that leaves the reactor should immediately rise to 100%. However, this was not the case. After running the experiment for several hours, 90% of the pipe reactor was plugged, which means that 90% of the reactor was filled with settled solids which did not move. So, only 10% of the reactor was available for flow. The suspension had to move through an ever smaller area, resulting in a higher velocity and a reduction in residence (reaction) time by 90%.
This Example illustrates the continuous preparation of quasi-crystalline boehmite from flash-calcined gibbsite using the decoupling method and apparatus according to the invention. The apparatus contained three conversion vessels with a total volume of 30 l.
31.70 kg water was added to a feed preparation vessel (1) of 250 l. Subsequently, 4.38 kg of 20 wt % nitric acid and 13.90 kg of flash-calcined gibbsite were added. The flash-calcined gibbsite contained 90.1 wt % solids. The resulting suspension was mixed.
The suspension was pumped to the first conversion vessel (3A). By way of steam injection the suspension was heated up to 190° C., thereby decreasing the solids to liquid ratio to 0.18.
The suspension was led through the subsequent two conversion vessels de-coupled temperatures (3B at 150° C.-3C at 170° C.). The average residence time in each of the three conversion vessels was 30 minutes. The suspension in all conversion vessels was agitated using a double-helix impeller at 76-83 rpm. The pressure of the whole system was controlled by a pressure valve positioned immediately beyond the third conversion vessel. The system pressure in this experiment was maintained at 12 bars. After the third conversion vessel the suspension was cooled down to 60° C. by a shell and tube heat-exchanger. Each reaction vessel was sampled and the rapidly cooled slurry was analyzed and compared with the final product.
The resulting final product was a peptized low-crystalline boehmite alumina. Rapid conversion in the first vessel at high temperature lead to high conversion and high crystal size. Quenching at 150° C. yielded a supersaturated solution, crystal size only slightly increases at an increase in conversion.
The elastic modulus G′ was determined.
In this example the experiment of Example 1 was repeated. However, now the temperature in the reaction vessel 3A was the same as 3B in Example 1, and vice versa. The temperatures in the reaction vessels are 3A 150° C., 3B 190° C. and 3C 170° C. The feed was prepared via the same procedure as in Example 1.
The suspension was pumped to the first conversion vessel (3A). By way of steam injection the suspension was heated up to 150° C., thereby decreasing the solids to liquid ratio to 0.19.
The suspension was led through the subsequent two conversion vessels (3B at 190° C.—3C at 170° C.). The average residence time in each of the three conversion vessels was 30 minutes. The suspension in all conversion vessels was agitated using a double-helix impeller at 76-83 rpm. The pressure of the whole system was controlled by a pressure valve positioned immediately beyond the third conversion vessel. The system pressure in this experiment was maintained at 12 bars. After the third conversion vessel the suspension was cooled down to 60° C. by a shell and tube heat-exchanger. Each reaction vessel was sampled and the rapidly cooled slurry was analyzed and compared with the final product.
Table 2 shows that this route, after treating the slurry at the same, but interchanged, temperatures in a decoupled system yields an improved product. At the same crystallinity, a material with smaller crystal sizes was obtained with no loss in surface areas. Stabilizing of the small crystals in the first vessel (3A) was followed by the conversion step at high temperature in vessel 3B. Quenching in vessel 3C prevented further crystal growth with a small additional conversion. The elastic modulus G′ of the various samples was determined.
By going first through a high elastic modulus (meaning gel-formation) a significant amount of stable nuclei was formed creating more seeds which resulted in a lower crystal size than example 1.
Direct comparison between the product of Example 1 and Example 2 in
| Number | Date | Country | Kind |
|---|---|---|---|
| 01202270.3 | Jun 2001 | EP | regional |
This application is a Continuation-in-Part of U.S. patent application Ser. No. 10/141,800, filed May 8, 2002, that claims priority of U.S. Patent Application Ser. No. 60/290,149, filed on May 10, 2001 and European Patent Application Ser. No. 01202270.3, filed on Jun. 13, 2001.
| Number | Date | Country | |
|---|---|---|---|
| 60290149 | May 2001 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10141800 | May 2002 | US |
| Child | 11143905 | Jun 2005 | US |
