The following relates to systems and methods for solid catalyst separation, in particular for slurry reactors such as hydrocracking reactors.
Bitumen, heavy oil or extra-heavy oil, collectively referred to herein as “heavy oil”, have a high viscosity and density, and thus are treated prior to being transported by pipeline. Heavy oil can be treated by adding a diluent to reduce the viscosity and density to a value that meets certain pipeline requirements. A significant amount of diluent may be required per volume of heavy oil, thus taking up corresponding pipeline capacity. Diluent is also separated at the receiving end, requiring additional capital cost and adding complexity to the treatment process.
Heavy oil feedstock can also be upgraded to synthetic crude oil, which can be processed directly in refineries. One process for upgrading heavy oil involves the addition of hydrogen, which reduces the molecular weight of the heavy oil and increases the hydrogen-to-carbon ratio. Improving the hydrogen-to-carbon ratio can also be achieved by a carbon rejection process (e.g., coking and de-asphalting the heavy oil).
Hydrogen addition processes include hydrocracking in the presence of a suitable catalyst. The catalyst is used to activate the added hydrogen and suppress the formation of gases and coke. The hydrogen addition processes typically utilize catalysts formulated from metals and the catalysts are tailored for selective conversion and high activity to maximize process throughput and output quality. Managing the use of catalysts in hydrocracking processes can affect which reactor type is used. The two main types of reactors are referred to as fixed bed reactors and slurry reactors. Several types of slurry reactors can be used, such as stirred tank reactors and bubble column and ebullated bed reactors.
Dispersed catalysts have been used in slurry reactors. These dispersed catalysts are colloidal suspensions of nanosized catalytic particles. In practice, a slurry that includes the heavy oil and finely dispersed catalyst is fed into a hydrocracking reactor. The high density of available reaction sites can avoid the plugging of pores that cause deactivation of the catalyst, however, maintaining uniform dispersion of the catalyst particles can be challenging and this process has typically been limited to hydrogen mixing in bubble column and ebullated bed reactors.
There are a few challenges for catalyst separation and solid handling after the slurry product exits a hydrocracking reactor. One challenge is the presence of solids in the product stream that can cause severe erosion in the pressure letdown system, for example, slurry pressure valves.
Another challenge is that the separation of solids from the product slurry typically requires expensive and labor-intensive processes such as filtration, centrifugation, or settling, all of which have challenges when faced with fine or ultrafine particles that may be present in a catalyst mixture. Moreover, the solid content specifications for crude oil being transported by pipeline is relatively low, e.g., 0.5 wt %. As such, a polishing step to remove fine particles may be required, further adding to the complexity and costs associated with the system.
Yet another challenge is that the separated catalyst particles can carry and entrain 10-80% of the treated oil, resulting in significant yield loss. Additionally, catalyst wash equipment should be used, further adding to the costs associated with the system.
The following system and method address certain challenges in upgrading heavy oil using a slurry reactor by transferring a solid phase in the treated slurry to a liquid phase in order to leverage the advantages of upgrading heavy oil using slurry reactors while reducing two-phase flow problems such as negative impacts on the subsequent letdown process and thus reduce capital and operating costs.
In one aspect, there is provided a method of processing a treated feed slurry produced by a slurry reactor, comprising mixing a chemical separation feed with the treated feed slurry produced by the slurry reactor to chemically separate solid catalyst particles in the treated feed slurry by dissolving the solid catalyst particles using an acid or base in the chemical separation feed.
In another aspect, there is provided a heavy oil upgrading process comprising the above method
In yet another aspect, there is provided a system for processing a treated feed slurry produced by a slurry reactor, comprising: a source of chemical separation feed, the chemical separation feed comprising an acid or a base; and a connection to an output line exiting the slurry reactor to mix the chemical separation feed with the treated feed slurry in the output line to chemically separate solid catalyst particles in the treated feed slurry by dissolving the solid catalyst particles using an acid or base in the chemical separation feed.
In yet another aspect, there is provided a heavy oil upgrading facility comprising the system.
Embodiments will now be described with reference to the appended drawings wherein:
The following system and method address certain challenges in upgrading heavy oil using a slurry reactor by converting a solid phase in the treated slurry to a liquid phase in order to leverage the advantages of upgrading heavy oil using slurry reactors while reducing two-phase flow problems. In particular, this conversion from a solid phase to a liquid phase can mitigate negative impacts on the subsequent pressure letdown components, e.g., due to erosion in the letdown valve, and reduce capital and operating costs by eliminating the need for enhanced materials in the letdown system or the need to separate the solid catalyst from the treated slurry to avoid such negative impacts.
The product slurry from a slurry reactor can be converted from a solid phase to a liquid phase by using an acidic or basic agent to dissolve the solid catalyst instead of requiring physical separation of the catalyst particles from the slurry. Dissolving and leaching of the catalyst particles can be done at the reactor temperature or lower. The process of dissolving the solid catalyst particles and eliminating the solid phase can effectively convert a solid-liquid process to a liquid-liquid process and make solid handling less complicated and less capital intensive. While certain examples used herein refer to hydrocracking or hydro processing more generally, the principles discussed herein can also be applied to any slurry reactor in which a solid catalyst is used and can be dissolved as herein described.
A slurry hydrocracking process is used to improve heavy oil properties such as density and viscosity, as well as to remove impurities. Due to a high asphaltene content in heavy oil, hydrocracking catalysts are prone to deactivation. In a slurry reactor, solid catalyst particles are typically dispersed or mixed with heavy oil before being fed into the reactor. The hydrocracking reaction takes place in the reactor and the particles are suspended in the reactor according to the type of reactor being used, for example, by hydrogen flow (i.e., bubble flow) and physical mixing. After the hydrocracking reactions terminate, the solid catalyst and treated oil are discharged from the reactor and the catalyst dissolved or “chemically separated” as described below to convert the solid phase to a liquid phase and mitigate negative impacts downstream, in particular on the letdown system.
As will be described below, the process and system described herein can also be integrated with advanced oil recovery processes such as a steam assisted gravity drainage (SAGD) process, where a SAGD emulsion can be added instead of water to the treated slurry. Adding and treating emulsion reduces oil/water separation and water load. The raw bitumen in the SAGD emulsion can blend with the treated heavy oil which could also improve the stability of the treated heavy oil, which is not currently leveraged in heavy oil slurry reaction processes. In addition, the direct addition of wellhead emulsion assists in the entire SAGD heat integration and a portion of water can be converted to steam for the SAGD process, thus further leveraging available sources to integrate the chemical separation technique described herein.
Moreover, since most olefins are with the light hydrocarbon, the olefins in the light end could react with water (in the presence of acid as catalyst) and convert to alcohols (hydration reactions).
Referring now to the figures,
The catalyst mixer 30 outputs a pumpable feed slurry 40. The feed slurry 40 is then fed to a heater 50 to heat the feed slurry 40 to a target reaction temperature for hydrocracking, for example by passing the feed slurry 40 through heating device(s) such as heat exchangers or a heater powered by a fuel or electricity. This results in a heated slurry 60 that is fed into a slurry hydrocracking reactor 80. The reactor 80 is also fed hydrogen 70 to perform the hydrocracking reaction. As indicated above, there are multiple types of slurry hydrocracking reactors 80, such as a stirred tank type reactor or a bubble column reactor, in which hydrogen is used to mix or suspend catalyst particles in the reactor 80.
The process described herein can be applied to either type of reactor 80 or any other slurry hydrocracking reactor 80 (or other slurry reactor) known in the art that produces a treated slurry 90 made up of treated oil with solid catalyst particles, which requires some form of separation to remove the solids from the treated oil. Normally, the treated slurry 90 would require a physical separation step, by settling, filtration, etc. In the process shown in
The choice of acid or base for use in the chemical separation feed is generally dependent on the particular catalyst 20 being used, i.e., according to which acid or base most effectively dissolves the particular catalyst. However, for the purposes of illustration, suitable acids can include strong acids, such as, HCl, H2SO4, H2S, HNO3, and combinations thereof.
Similarly, while the choice of a suitable base will depend on the catalyst 20 being used, for the purposes of illustration, suitable bases can include strong bases, such as, NaOH, KOH, and combinations thereof.
It can be appreciated that the water used to introduce the acid or base can be provided from any available source. Advantageously, an emulsion that includes water can be combined with the acid or base to create the chemical separation feed 100. The emulsion would provide water to carry the acid or base and would also be lightened when combined with the treated oil in the slurry 90 to facilitate later separation, which is not currently leveraged in existing heavy oil upgrading processes. Moreover, lighter oil produced in the hydrocracking process may need to be blended with the emulsion to meet certain pipeline specifications. That is, the use of an emulsion rather than normal feedwater can be strategic as well as convenient. The emulsion can be obtained from an existing oil recovery site such as a SAGD operation. Other sources of water such as blowdown water or other recycled or reused water can be used, with suitable treatments applied if necessary. For example, SAGD boilers generate blowdown water, which is already basic and can be used for this purpose. It may be noted that any such source of water should be tested to ensure suitable reactivity, e.g., to determine if there are any species of concern in the water.
The treated slurry 90 exits the reactor 80 at a relatively high velocity. In existing systems, when the catalyst exits the reactor in solid form, this can cause major problems, such as erosion, when passing through a pressure letdown valve 120 used to reduce the pressure in the system. This problem is known in the art of heavy oil upgrading and has led to the use of expensive materials in the letdown system (e.g., enhanced erosion-resistant materials) or requires physical separation of the catalyst prior to passing through the letdown valve. In the present solution, by mixing the chemical separation feed 100 with the treated slurry 90 before the pressure letdown valve 120, the mixture 110 (which includes dissolved catalyst rather than solid particles) passes through the letdown valve 120. Since the mixture 110 includes dissolved catalyst (single phase) rather than suspended solid catalyst (two phase), the negative impacts on the pressure letdown valve 120 can be mitigated or even eliminated without the need for expensive materials or additional separation equipment. That is, the dissolved catalyst effectively converts the two phase (solid and liquid) treated slurry 90 to a single phase (liquid) or two-phase (liquid-liquid) mixture 110 to lessen the negative impacts on the letdown system. A letdown feed 130 may then be subjected to various downstream operations. For example, as shown in
Referring now to
It can be appreciated that other downstream processes can also be incorporated, such as recycling recovered hydrogen (not shown) and feeding the recycled hydrogen back to the reactor 80. For example, hydrogen that leaves the reactor with the light ends 85 can be separated from the light ends 85 then cleaned and reused.
The treated slurry 90 is then mixed with a chemical separation feed 100 at step 406. As indicated above, the chemical separation feed 100 refers to a combination of an acid or base and water or an emulsion (containing water). This step chemically separates the solid catalyst particles suspended in the treated slurry 90 by dissolving the solid catalyst and effectively converting a solid-liquid two-phase feed into a liquid-liquid phase feed. By dissolving the catalyst particles at step 406 and prior to step 408, which reduces the pressure of the feed at a pressure letdown valve 120, issues normally associated with a slurry flow through such a letdown valve 120 can be mitigated.
At step 410, the treated oil 150 can be separated from the water/emulsion containing the acid/base, and the dissolved particles, to allow the treated oil to be transported or subsequently processed. Optionally, as shown in dashed lines, steam 170 can be generated, e.g., using a three-phase separator 145.
Steps 412 and 414 can also be optionally performed to recover the catalyst by separating the dissolved particles from the acid/base and water/emulsion at step 412 and recycling the recovered catalyst 200 at step 414.
Turning now to
Below is a series of tables illustrating example values used in the simulation shown in
For simplicity and clarity of illustration, where considered appropriate, reference numerals may be repeated among the figures to indicate corresponding or analogous elements. In addition, numerous specific details are set forth in order to provide a thorough understanding of the examples described herein. However, it will be understood by those of ordinary skill in the art that the examples described herein may be practiced without these specific details. In other instances, well-known methods, procedures and components have not been described in detail so as not to obscure the examples described herein. Also, the description is not to be considered as limiting the scope of the examples described herein.
It will be appreciated that the examples and corresponding diagrams used herein are for illustrative purposes only. Different configurations and terminology can be used without departing from the principles expressed herein. For instance, components and modules can be added, deleted, modified, or arranged with differing connections without departing from these principles.
The steps or operations in the flow charts and diagrams described herein are just for example. There may be many variations to these steps or operations without departing from the principles discussed above. For instance, the steps may be performed in a differing order, or steps may be added, deleted, or modified.
Although the above principles have been described with reference to certain specific examples, various modifications thereof will be apparent to those skilled in the art as outlined in the appended claims.
This application claims priority to U.S. Provisional Patent Application No. 63/027,585 filed on May 20, 2020, entitled “System and Method for Solid Catalyst Separation In Slurry Reactors” and the entire contents of which is incorporated herein by reference.
Number | Date | Country | |
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63027585 | May 2020 | US |