Patent Application
20090159501
This invention relates to the electrodesulfurization of heavy oil feedstreams. The heavy oil feedstreams, along with hydrogen, is passed the cathode side of an electrochemical cell wherein the organically bound sulfur compounds in the heavy oil are reduced and the sulfur is released as hydrogen sulfide. The hydrogen sulfide can be fed directly into the anode side of the electrochemical cell to produce sulfur and hydrogen or it can be passed to an oxidation zone containing an aqueous solution of an oxidized metal salt.
Bitumen, in this case, refers to the naturally occurring heavy oil deposits such as the Canadian bitumens found in Cold Lake and Athabasca. Bitumen is a very complex mixture of chemicals and typically contains hydrocarbons, heteroatoms, metals and carbon chains in excess of 2,000 carbon atoms. A variety of technologies are used to upgrade heavy oils, including bitumens. Such technologies include thermal conversion, or coking, that involves using heat to break the long heavy hydrocarbon molecules. Thermal conversion includes such processes as delayed coking and fluid coking. Delayed coking is a process wherein a heavy oil stream is heated to about 932° F. (500° C.) then pumped into one side of a double-sided coker where it cracks into various products ranging from solid coke to vapor products. Fluid coking is similar to delayed coking except it is a continuous process. In fluid coking, the heavy oil stream is heated to about 932° F. (500° C.), but instead of pumping the heavy oil to a coker it is sprayed in a fine mist around the entire height and circumference of the coker. The heavy oil cracks into a vapor and the resulting coke is in the form of a powder-like form, which can be drained from the bottom of the coker.
Another technology used to upgrade heavy oils is catalytic conversion which is used to crack larger molecules into smaller, refineable hydrocarbons in the presence of a cracking catalyst. High-pressure hydrogen is often used in catalytic conversion. While catalytic conversion is more expensive than thermal conversion, it produces a higher yield of upgraded value product.
Distillation is also used for upgrading heavy oils including bitumens wherein the heavy oil is distilled in a distillation tower into a variety of products that boil at different temperatures. The lightest hydrocarbons with the lowest boiling points travel as a vapor to the top of the tower. Heavier and denser hydrocarbons with higher boiling points collect as liquids lower in the tower.
While the above mentioned technologies are useful for converting a portion of heavy oils to lighter and more valuable products, such technologies are not particularly useful for reducing the sulfur content of such feedstocks. One important technology that has been used to reduce the sulfur content (as well as nitrogen and trace metal content) from such feedstocks is hydrotreating. In hydrotreating, or hydrodesulfurization, the heavy oil is contacted with hydrogen and a suitable desulfurization catalyst at elevated pressures and temperatures. The process typically requires the use of hydrogen pressures ranging preferably from about 700 to about 2,500 psig and temperatures ranging from about 650° F. (343° C.) to about 800° F. (426° C.), depending on the nature of the feedstock to be desulfurized and the amount of sulfur required to be removed.
Hydrotreating is efficient in the case of distillate oil feedstocks but less efficient when used with heavier feedstocks such as bitumens and residua. This is due to several factors. First, most of the sulfur in such feedstocks is contained in high molecular weight molecules, and it is difficult for them to diffuse through the catalyst pores to the catalyst surface. Furthermore, once at the surface, it is difficult for the sulfur atoms contained in these high molecular weight molecules to sufficiently contact the catalyst surface. Additionally, such feedstocks may contain large amounts of asphaltenes that tend to form coke deposits on the catalyst surface under the process conditions, thereby leading to deactivation of the catalyst. Moreover, high boiling organometallic compounds present in such oil feedstocks decompose and deposit metals on the catalyst surface thereby diminishing the catalyst life time. Severe operating conditions cause appreciable cracking of high boiling oils thereby producing olefinic fragments which, themselves, consume hydrogen, thereby lowering the process efficiency and increasing costs.
Alternate desulfurization processes that have been employed in the past utilizing alkali metal dispersions, such as sodium, as desulfurization agents. One example of such a process involves contacting a hydrocarbon fraction with a sodium dispersion. The sodium reacts with the sulfur to form dispersed sodium sulfide (Na2S). However, such a process has not proven to be attractive, particularly for treatment of high boiling, high sulfur content feedstocks due to: (a) the high cost of sodium, (b) problems related to removal of sodium sulfide formed in the process, (c) the impracticability of regenerating sodium from the sodium sulfide, (d) the relatively low desulfurization efficiency due, in part, to the formation, of substantial amounts of organo-sodium salts, (e) a tendency to form increased concentrations of high molecular weight polymeric components (asphaltenes), and (f) the failure to adequately remove metal contaminants (iron, nickel, vanadium) from the feed as is observed in the competitive catalytic hydrodesulfurization process.
While various attempts have been made to mitigate some of the above-mentioned problems, low desulfurization efficiency has still remained an unsolved problem. It has been speculated that the low efficiency is due in part to the formation of organo-sodium compounds formed either by reaction of the sodium with acidic hydrocarbons, addition of sodium to certain reactive olefins or as products obtained when sodium cleaves certain of the organic ethers, sulfides and amines contained in the oil. Formation of these organo-sodium compounds, which are desulfurization inactive materials, effectively removes a portion of the sodium that otherwise would be available for the desulfurization reaction. Sodium in excess of the theoretical amount for desulfurization must therefore be added to compensate for organo-sodium compound formation. Moreover, a hydrocarbon insoluble sludge which forms in the course of the sodium-treating reaction (apparently comprised primarily of organo-sodium compounds), makes the reaction mixture extremely viscous and hence impairs mixing and heat transfer performance in the reactor.
Some work has been done to develop electrochemical processes to desulfurize crudes and heavy oils, such as bitumen. Electrochemical processes, such as that taught in U.S. Pat. No. 6,877,556 require the use of reagents such as solvents, electrolytes, or both. Use of such expensive reagents adds to the complexity of those processes since their recovery from the bitumen is required for economic reasons such processes are not commercially practiced.
Therefore, there remains a need in the art for improved process technology-capable of effectively and economically removing sulfur from heavy petroleum feedstock.
In accordance with a preferred embodiment of the present invention there is provided a process for removing sulfur from heavy oil feedstreams containing sulfur-containing molecules, which process comprises:
a) heating and pressurizing said heavy oil feedstream to a temperature of about 400° F. (204° C.) to about 800° F. (426° C.) and a pressure of about 200 psig to about 700 psig;
b) passing said heated and pressurized heavy oil feedstream and an effective amount of a hydrogen source to the cathode side of a desulfurization electrochemical cell containing at least one cathode side and at least one anode side separated by an ion-permeable membrane and subjecting the heavy oil feedstream to a voltage in the range of about 4V to about 500V and a current density of about 10 mA/cm2 to about 1000 mA/cm2, thereby reducing at least a portion of the sulfur-containing molecules to hydrogen sulfide and resulting in a sulfur-lean heavy oil feedstream and hydrogen sulfide;
c) separating said hydrogen sulfide from said sulfur-lean heavy oil feedstream in a gas/liquid separation zone; and
d) introducing at least a portion of said hydrogen sulfide into the anode side of said desulfurization electrochemical cell wherein it is oxidized to produce elemental sulfur and hydrogen ions, and at least a portion of the hydrogen ions migrate to the cathode side of said desulfurization electrochemical cell.
Also in accordance with the present invention there is provided a process for removing sulfur from heavy oil feedstreams containing sulfur-containing molecules, which process comprises:
a) heating and pressurizing said heavy oil feedstream to a temperature of about 400° F. (204° C.) to about 800° F. (426° C.) and a pressure of about 200 psig to about 700 psig;
b) passing the heated and pressurized heavy oil feedstream and an effective amount of a hydrogen source to the cathode side of a desulfurization electrochemical cell containing at least one cathode side and at least on anode side and subjecting the heavy oil feedstream to a voltage in the range of about 4V to about 500V and a current density of about 10 mA/cm2 to about 1000 mA/cm2, thereby reducing at least a portion of the sulfur-containing molecules to hydrogen sulfide and resulting in a sulfur-lean heavy oil feedstream and hydrogen sulfide;
c) separating said hydrogen sulfide from said sulfur-lean heavy oil feedstream in a gas/liquid separation zone;
d) passing at least a portion of said hydrogen sulfide to a hydrogen sulfide oxidation zone containing a aqueous solution of an oxidized metal salt wherein the metal cation in the aqueous solution has an oxidation potential high enough to oxidize hydrogen sulfide to produce elemental sulfur, hydrogen ions and reduced metal ions;
e) separating and recovering the elemental sulfur;
f) passing said aqueous solution of hydrogen ions and reduced metal ions to the anode side of said electrochemical cell, wherein at least a portion of the reduced metal salts are reoxidized and at least a portion of the hydrogen ions migrate to the cathode side of said electrochemical cell to form hydrogen gas; and
g) passing at least a portion of the oxidized metal salts back to the hydrogen sulfide oxidation zone.
In a preferred embodiment, at least about a 10 wt. % fraction of the heavy oil feedstream boils at a temperature of at least about 1050° F. (565° C.).
In another preferred embodiment, the hydrogen source is selected from water and hydrogen gas.
In another preferred embodiment the heavy oil feedstream is a bitumen.
The process of the present invention is preferably practiced on sulfur-containing heavy oil feedstreams. In a preferred embodiment of the present invention, the heavy oil feedstreams contains at least about 10 wt. % of material boiling in excess of about 1050° F. (565° C.) at atmospheric pressure (defined as 0 psig), more preferably at least about 25 wt. % of material boiling above about 1050° F. (565° C.) at atmospheric pressure. Unless otherwise noted, all boiling temperatures herein are designated at atmospheric pressure (defined as 0 psig). Non-limiting examples of such feedstreams include whole, topped or froth-treated bitumens, heavy oils, whole or topped crude oils and residua. These include crude oils obtained from any area of the world, as well as heavy gas oils, shale oils, tar sands or syncrude derived from tar sands, coal oils, and asphaltenes. Additionally, both atmospheric residuum, boiling above about 650° F. (343° C.) and vacuum residuum, boiling above about 1050° F. (565° C.) can be treated in accordance with the present invention. The preferred feedstream to be treated in accordance with the present invention is bitumen. Bitumen is generally defined as a mixture of organic liquids that are highly viscous, black, sticky and composed primarily of highly condensed polycyclic aromatic hydrocarbons. Bitumen is obtained from extraction from oil shales and tar sands. Such heavy feedstreams contain an appreciable amount of so-called “hard” sulfur such as dibenzothiophenes (DBTs) that are very difficult to remove by conventional means.
These heavy feedstreams are sometimes desulfurized with use of sodium, as previously mentioned. In the sodium upgrading of bitumen, elemental sodium acts as a chemical reductant, each sodium atom transferring a single electron to molecules in the bitumen thereby initiating free radical desulfurization chemistry. In the electrochemical process of the present invention, reduction, or the generation of free radicals by transfer of electrons, is accomplished by use of an electrode polarized to the reducing potential of the target sulfur-containing molecules. The primary of advantage of this invention is that the sulfur is released from the heavy oil as hydrogen sulfide, in contrast to being released as sodium sulfide when sodium is used. Regeneration of elemental sodium from sodium sulfide is currently the critical technological limitation of the sodium process. The hydrogen sulfide produced by the practice of the present invention can be converted to sulfur in a Claus plant. The Claus process is well known in the art and is a gas desulfurizing process for recovering elemental sulfur from gaseous hydrogen sulfide. Typically gaseous streams containing at least about 25% hydrogen sulfide are suitable for a Claus plant. The Claus process is a two step process, thermal and catalytic. In the thermal step, hydrogen sulfide-laden gas reacts in a substoichiometric combustion at temperatures above about 1562° F. (850° C.) such that elemental sulfur precipitates in a downstream process gas cooler. The Claus reaction continues in a catalytic step with activated alumina or titanium dioxide, and serves to boost the sulfur yield. Further, the resulting sulfur-lean heavy oil product stream, or bitumen, is similar to that produced by the sodium process. The number of electrons required to initiate the radical chemistry in the process of the present invention will be roughly equivalent to the number required to regenerate sodium in the sodium treating process.
The process of the present invention does not require the addition of an electrolyte to the heavy oil feedstream, but rather, relies on the intrinsic conductivity of the heavy oil feedstream at elevated temperatures. It will be understood that the term “heavy oil” as used herein includes both bitumen and heavy oil petroleum feedstreams, such as crude oils, atmospheric resids, and vacuum resids. This process is preferably utilized to upgrade bitumens and/or crude oils that have an API gravity less than 15. The inventors hereof have undertaken studies to determine the electrochemical conductivity of crudes and residues (which includes bitumen and heavy oils) at temperatures up to about 572° F. (300° C.) and have demonstrated an exponential increase in electrical conductivity with temperature as illustrated in
A 4 mA/cm2 electrical current density at 662° F. (350° C.) with an applied voltage of 150 volts and a cathode-to-anode gap of 1 mm was measured for an American crude oil. Though this is lower than would be utilized in preferred commercial embodiments of the present invention, the linear velocity for this measurement was lower than the preferred velocity ranges by about three orders of magnitude: 0.1 cm/s vs. 100 cm/s. Using a 0.8 exponent for the impact of increased flow velocity on current density at an electrode, it is estimated that the current density would increase to about 159 mA/cm2 at a linear velocity of about 100 cm/s. This suggests that more commercially attractive current densities achieved at higher applied voltages. Narrower gap electrode designs or fluidized bed electrode systems could also be used to lower the required applied voltage.
Two preferred embodiments are presented in this application. The first is represented in
The resulting product stream which is comprised of elemental sulfur, hydrogen ions, and reduced metal ions is passed via line 118 from the hydrogen sulfide oxidation zone OX to second separation zone SZ2 wherein the sulfur is removed via line 120 and the hydrogen ions and reduced metal ions are passed via line 122 to the anode side A of said electrochemical cell wherein the reduced metal ions are re-oxidized to their original state and the hydrogen ions migrate to the cathodic side through ion conducting membrane S to produce molecular hydrogen. Preferably, at least a portion of the re-oxidized metal ions are sent back to the hydrogen sulfide oxidation zone OX via line 124. Thus, the cathodic side of an electrochemical cell is used for electrodesulfurization while the anodic side is used for metal ion re-oxidation. H2S oxidation to sulfur is achieved chemically (or directly) in the oxidation zone OX by the re-oxidized metal ions.
The present invention will be better understood with reference to the following examples that are presented herein for illustrative purposes only and are not to be taken as being limiting in any manner.
For the following examples, a 300-cc autoclave (Parr Instruments, Moline, Ill.) was modified to allow two insulating glands (Conax, Buffalo, N.Y.) to feed through the autoclave head. Two cylindrical stainless steel (316) mesh electrodes were connected to the Conax glands, where a power supply (GW Laboratory DC Power Supply, Model GPR-1810HD) was connected to the other end. The autoclave body was fitted with a glass insert, a thermal-couple and a stirring rod. The autoclave was charged with the desired gas under pressure and run either in a batch mode or a flow-through mode.
To the glass insert was added 1.0 g of dibenzothiophene (DBT), 3.87 g tetrabutylammonium hexafluorophosphate (TBAPF6), and 100 milliliter (“ml”) anhydrous dimethyl sulfoxide (DMSO, Aldrich). After the content was dissolved, the glass insert was loaded into the autoclave body, the autoclave head assembled and pressure tested. The autoclave was charged with 70 psig of N2 and heated to 212° F. (100° C.) with stirring (300 rpm). A voltage of 5 Volts was applied and the current was 0.8 Amp. The current gradually decreased with time and after two hours, the run was stopped. The autoclave was opened and the content acidified with 10% HCl (50 ml). The acidified solution was then diluted with 100 ml of de-ionized (“DI”) water, extracted with ether (50 ml×3). The ether layer was separated and dried over anhydrous Na2SO4, and ether was allowed to evaporate under a stream of N2. The isolated dry products were analyzed by GC-MS. A conversion of 12% was found for DBT and the products are as the following.
This example shows that the electrochemical reduction of DBT under N2 resulted in: 12% DBT conversion after 2 h at 212° F. GC-MS revealed that the products consisted of 35% 2-phenyl benzenethiol, 8% tetrahydro-DBT, and 57% of a species with a mass of 214. The assignment of this peak as 2-phenyl benzenethiol was done by comparing with an authentic sample. The mass 214 species was tentatively assigned as 2-phenyl benzenethiol with two methyl groups added. Addition of methyl groups to DBT indicates that decomposition of solvent DMSO occurred since it is the only source of methyl groups in this system. No desulfurization product biphenyl was observed in this run.
To the glass insert was added 0.5 g DBT, 3.87 g tetrabutylammonium hexafluorophosphate (TBAPF6), and 100 ml anhydrous dimethyl sulfoxide (DMSO, Aldrich). After the content was dissolved, the glass insert was loaded into the autoclave body, the autoclave head assembled and pressure tested. The autoclave was charged with 300 psig of H2 and heated to about 257° F. (125° C.) with stirring at about 300 rpm. A voltage of 4.5 Volts was applied and the current was 1.0 Amp. The current gradually decreased with time and after three and half (3.5) hours, the run was stopped. The autoclave was opened and the content acidified with 10% HCl (50 ml). The acidified solution was then diluted with 100 ml of DI water, extracted with ether (50 ml×3). The ether layer was separated and dried over anhydrous Na2SO4, and ether was allowed to evaporate under a stream of N2. The isolated dry products were analyzed by GC-MS. A conversion of 16.5% was found for DBT and the products are as the following.
To the glass insert was added 1.0 g 4,6-diethyl dibenzothiophene (DEDBT), 3.87 g tetrabutylammonium hexafluorophosphate (TBAPF6), and 100-mL anhydrous dimethyl sulfoxide (DMSO, Aldrich). After the content was dissolved, the glass insert was loaded into the autoclave body, the autoclave head assembled and pressure tested. The autoclave was charged with 200 psig of H2 and heated to about 212° F. with stirring (300 rpm). A voltage of 7 Volts was applied and the current was 1.0 Amp. The current gradually decreased with time and after two and half (2.5) hours, the run was stopped. The autoclave was opened and the content acidified with 10% HCl (50 ml). The acidified solution was then diluted with 100 ml of DI water, extracted with ether (50 ml×3). The ether layer was separated and dried over anhydrous Na2SO4, and ether was allowed to evaporate under a stream of N2. The isolated dry products were analyzed by GC-MS. A conversion of 16% was found for DEDBT and the products are as the following.
Similarly, desulfurization was also observed for sterically hindered Diethyl Dibenzothiophene (DEDBT) under H2. The conversion was ca. 16% and the products contained 53% desulfurized compounds, 46% dihydro-DEDBT and a trace amount of tetrahydro-DEDBT. Solvent decomposition also occurs in this case. Although electrochemical desulfurization of DBT and hindered DBT has been achieved under H2 in the 212° F. to 257° F. (100° to 125° C.) temperature range, the conversion is still quite low.
As a proof of concept, it is critical to demonstrate that high conversion and high degree of desulfurization can be achieved. In this example, it was discovered that, at room temperature, the DMSO/Bu4NPF6 system allows the electrochemical reduction of DBT to be run for an extended period of time. Thermal degradation of the solvent/electrolyte is minimal at room temperature. Conversion of DBT and product distribution is listed in Table 1. Each row in the table represents a separate experiment run under identical conditions except for the length of electrolysis (0.5 g DBT, 4.0 g Bu4NPF6, 100 ml DMSO, 300 psig H2, 4.5 V cell voltage, 77° F. (25° C.), acidic work-up). The electrolysis is clean under these conditions; and the products were isolated following the acidic work-up procedures and analyzed by GC-MS. The assignment for DBT-H2Me3 is tentative; assignments for other products are of high confidence, either by comparing with authentic samples or by good-quality match to the standard in the mass spectrum library. At short run time (3 h and 17 h), the products are 100% desulfurized. As the conversion goes up with increasing run time, small amounts of 2-phenyl benzenethiol and methylated DBT were observed. A small amount of heavy product, tetraphenyl, was also found at long run length (72 h and 163.5 h), which was probably formed from secondary electrochemical reactions. A conversion of 94% was achieved in a week, with the desulfurized products accounting for ˜98% of the products. The overall degree of desulfurization is >90%. The conversion appears to follow first-order kinetics, with a simulated rate constant of 3.5×10−6 s−1 at room temperature (
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This Application claims the benefit of U.S. Provisional Application No. 61/008,416 filed Dec. 20, 2007.
| Number | Date | Country | |
|---|---|---|---|
| 61008416 | Dec 2007 | US |
