Electrolysis is a very important industrial process used to produce a variety of vital chemical building blocks. Processes such as the chlor-alkali process, electro-synthesis of anthraquinone, and electro-fluoridation all play essential roles in the production of chemicals used in our everyday lives. Electrolysis can be an energy efficient process with a significantly lower carbon footprint compared to traditional thermal catalysis processes if the input electricity is derived from a renewable resource such as wind or solar. As of 2006, chemical production by electrochemical processes made up more than 6% of the total electrical generating capacity of the United States, with the most energy intensive process as being performed by the chlor-alkali industry. These processes are used to produce hydrogen gas, caustic soda (sodium hydroxide), and chlorine gas. For the chlor-alkali processes, and most electrolysis processes, the economics are dominated by the cost of electricity, which accounts for a significant fraction of the total manufacturing cost. However, the decreasing costs of electricity from renewable resources and the continued adoption of time-of-use pricing schemes are likely to change the economics of electrochemical processes, shifting importance towards decreasing the capital cost of the electrolyzer system itself.
The process chemistry of the chlor-alkali process is relatively simple but the operational and reactor design issues are vastly complex. The most energy efficient electrolyzer in the chlor-alkali industry is the membrane electrolyzer. The membrane electrolyzer functions by separating anolyte and catholyte streams by means of an ion selective membrane and that only allows cationic species (e.g. Na+, K+, H+) and small amounts of water to pass through it. Diaphragm electrolyzers and mercury electrolytic cells are also used to produce bases, although these technologies are being phased out in favor of membrane reactors. This is due to health and environmental concerns relating to the use of asbestos and mercury, respectively. Key challenges with membrane electrolyzers include the high cost of the ion-selective membranes and their susceptibility to fouling. Further, electrodialysis cells typically rely on multiple membranes and operate at low current densities. Various approaches have been pursued in order to improve the yield, energy efficiency, economics, and environmental impacts of the membrane process.
Accordingly, some embodiments of the present disclosure relates to a system for treatment of brines including one or more electrolyzers, each electrolyzer including an influent flow chamber including an influent stream; at least one anode effluent flow chamber including an anode effluent stream; at least one cathode effluent flow chamber including a cathode effluent stream; at least one porous anode positioned at a location within and extending longitudinally along the influent flow chamber, and further positioned to separate the influent flow chamber from the at least one anode effluent flow chamber; and at least one porous cathode positioned at a location within and extending longitudinally along the influent flow chamber, and further positioned to separate the influent flow chamber from the at least one cathode effluent flow chamber, wherein the at least one anode and at least one cathode are positioned obliquely to each other. In some embodiments, the system includes an anode effluent processing unit in fluid communication with the at least one anode effluent flow chamber; a cathode effluent processing unit in fluid communication with the at least one cathode effluent flow chamber; a neutralization unit producing a system effluent stream, the neutralization unit positioned in fluid communication with the anode effluent processing unit, the cathode effluent processing unit, or combination thereof; and a brine inlet stream in fluid communication with the one or more electrolyzers, the anode effluent processing unit, the cathode effluent processing unit, or combinations thereof, and configured to provide a source of brine to the one or more electrolyzers. In some embodiments, the at least one porous anode and the at least one porous cathode include a catalyst layer and a semi-permeable layer disposed on the catalyst layer, the semi-permeable layer being selectively permeable to one or more components of the influent stream.
In some embodiments, the anode effluent stream includes an acid effluent stream and the cathode effluent stream includes a basic effluent stream and a hydrogen gas stream. In some embodiments, the at least one anode effluent flow chamber and at least one cathode effluent flow chamber each include a fluid effluent outlet and a gas effluent outlet.
In some embodiments, the at least one anode includes a plurality of anode fingers and the at least one cathode includes a plurality of cathode fingers, wherein the plurality of anode fingers and the plurality of cathode fingers are interdigitated. In some embodiments, the one or more electrolyzers include a plurality of electrolyzers arranged in series, wherein the influent flow chambers of the plurality of electrolyzers are in fluid communication; the anode effluent flow chambers of the plurality of electrolyzers are in fluid communication; and the cathode effluent flow chambers of the plurality of electrolyzers are in fluid communication.
In some embodiments, one or more recycle flow chambers are configured to recycle at least a portion of the anode effluent stream, the cathode effluent stream, or combinations thereof, to a previous electrolyzer in the plurality of electrolyzers. In some embodiments, the cathode effluent processing unit is in fluid communication with the brine inlet stream, a carbon dioxide inlet stream, or combinations thereof.
In some embodiments, the system includes a separation unit configured to separate the basic effluent stream into an alkaline product stream and an alkaline salt water stream, the separation unit in fluid communication with the cathode effluent processing unit, one or more electrolyzers, and the neutralization unit. In some embodiments, the influent stream includes at least a portion of the alkaline salt water stream. In some embodiments, the alkaline product stream includes alkali earth metal carbonates, alkali earth metal hydroxides, or combinations thereof. In some embodiments, the system effluent stream includes concentrated carbon dioxide, demineralized salt water, sterilized salt water, neutralized salt water, or combinations thereof. In some embodiments, the acid effluent stream includes a chlorine gas stream and the anode effluent processing unit includes a fuel cell, wherein the fuel cell is in fluid communication with the chlorine gas stream and the hydrogen gas stream. In some embodiments, the influent stream includes at least a portion of the system effluent stream. In some embodiments, the influent stream includes neutralized salt water from the neutralization unit.
Some embodiments of the present disclosure relates to a method for treatment of brines including providing one or more electrolyzers, each electrolyzer including an influent flow chamber; at least one anode effluent flow chamber; at least one cathode effluent flow chamber; at least one porous anode positioned at a location within and extending longitudinally along the influent flow chamber, and further positioned to separate the influent flow chamber from the at least one anode effluent flow chamber; and at least one porous cathode positioned at a location within and extending longitudinally along the influent flow chamber, and further positioned to separate the influent flow chamber from the at least one cathode effluent flow chamber, wherein the at least one anode and at least one cathode are positioned obliquely to each other.
In some embodiments, the method includes providing an influent stream to the influent flow chamber, the influent stream including at least one reactant; applying a voltage across the at least one porous anode and the at least one porous cathode; flowing the influent stream through the at least one porous anode and the at least one porous cathode; isolating an anode effluent stream in the at least one anode effluent flow chamber and a cathode effluent stream in the at least one cathode effluent flow chamber, wherein the anode effluent stream includes an acid effluent stream and the cathode effluent stream includes a basic effluent stream and a hydrogen gas stream; providing at least a portion of the anode effluent stream to an anode effluent processing unit; providing at least a portion of the cathode effluent stream to a cathode effluent processing unit; flowing a brine inlet stream, a carbon dioxide inlet stream, or combinations thereof into the cathode effluent processing unit; providing a stream from the anode effluent processing unit and the cathode effluent processing unit to a neutralization unit; and producing a system effluent stream from the neutralization unit. In some embodiments, the method includes separating the cathode effluent stream from the cathode effluent processing unit into an alkaline product stream and an alkaline salt water stream, wherein the alkaline product stream includes alkali earth metal carbonates, alkali earth metal hydroxides, or combinations thereof and recycling at least a portion of the alkaline salt water stream in the influent stream. In some embodiments, the system effluent stream includes concentrated carbon dioxide, demineralized salt water, sterilized salt water, neutralized salt water, or combinations thereof.
Some embodiments of the present disclosure relates to a method for treatment of brines including providing one or more electrolyzers, each electrolyzer including an influent flow chamber; at least one anode effluent flow chamber; at least one cathode effluent flow chamber; at least one porous anode positioned at a location within and extending longitudinally along the influent flow chamber, and further positioned to separate the influent flow chamber from the at least one anode effluent flow chamber; and at least one porous cathode positioned at a location within and extending longitudinally along the influent flow chamber, and further positioned to separate the influent flow chamber from the at least one cathode effluent flow chamber, wherein the at least one anode and at least one cathode are positioned obliquely to each other, and the at least one anode effluent flow chamber and at least one cathode effluent flow chamber each include a fluid effluent outlet and a gas effluent outlet.
In some embodiments, the method includes providing an influent stream to the influent flow chamber, the influent stream including at least one reactant; applying a voltage across the at least one porous anode and the at least one porous cathode; flowing the influent stream through the at least one porous anode and the at least one porous cathode; isolating an anode effluent stream in the at least one anode effluent flow chamber and a cathode effluent stream in the at least one cathode effluent flow chamber, wherein the anode effluent stream includes an acid effluent stream and an oxygen gas stream and the cathode effluent stream includes a basic effluent stream and a hydrogen gas stream; providing one or more recycle flow chambers configured to recycle at least a portion of the anode effluent stream, the cathode effluent stream, or combinations thereof, to the one or more electrolyzers; providing at least a portion of the acid effluent stream to an anode effluent processing unit; providing at least a portion of the basic effluent stream to a cathode effluent processing unit; flowing a brine inlet stream, a carbon dioxide inlet stream, or combinations thereof into the cathode effluent processing unit providing a stream from the anode effluent processing unit to a neutralization unit; separating the cathode effluent stream from the cathode effluent processing unit into an alkaline product stream and an alkaline salt water stream, wherein the alkaline product stream includes alkali earth metal carbonates, alkali earth metal hydroxides, or combinations thereof; recycling a first portion of the alkaline salt water stream in the influent stream; flowing a second portion the alkaline salt water stream to the neutralization unit; and producing a system effluent stream from the neutralization unit. In some embodiments, the system effluent stream includes concentrated carbon dioxide, demineralized salt water, sterilized salt water, neutralized salt water, or combinations thereof.
The drawings show embodiments of the disclosed subject matter for the purpose of illustrating the invention. However, it should be understood that the present application is not limited to the precise arrangements and instrumentalities shown in the drawings, wherein:
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At least one porous anode 204A is positioned at a location within influent flow chamber 202. In some embodiments, anode 204A extends longitudinally along influent flow chamber 202, e.g., in the direction of flow of influent stream 104. In some embodiments, anode 204A is positioned at an oblique angle to the direction of flow of influent stream 104. In some embodiments, anode 204A is positioned to separate influent flow chamber 202 from anode effluent flow chamber 204. In some embodiments, anode 204A extends across an entire width of anode effluent flow chamber 204. In some embodiments, anode 204A is a wire mesh electrode of any suitable shape.
At least one porous cathode 206A is positioned at a location within influent chamber 202. In some embodiments, cathode 206A extends longitudinally along influent flow chamber 202, e.g., in the direction of flow of influent stream 104. In some embodiments, cathode 206A is positioned at an oblique angle to the direction of flow of influent stream 104. In some embodiments, cathode 206A is positioned to separate influent flow chamber 202 from a cathode effluent flow chamber 206. In some embodiments, cathode 206A extends across an entire width of cathode effluent flow chamber 206. In some embodiments, cathode 206A is a wire mesh electrode of any suitable shape.
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As voltage is applied across the anode 204A/cathode 206A pair, ionic current passes between the two porous electrodes by transport of anion (A−) and cation (X+) species in influent stream 104, resulting in electrochemical reactions at anode 204A and cathode 206A. These electrochemical reactions result in effluent streams 106 discussed above. In some embodiments, the electrochemical reactions at anode 204A generate an anode effluent stream 204S in anode effluent flow chamber 204. In some embodiments, anode effluent stream 204S includes an acid effluent stream 208A. In some embodiments, acidic stream 106B includes acidic effluent stream 208A, as will be discussed in greater detail below. In some embodiments, anode effluent stream 204S includes a gaseous stream 208G. In some embodiments, acidic stream 106B includes gaseous stream 208G. In some embodiments, gaseous stream 208G includes oxygen gas, chlorine gas, or combinations thereof. In some embodiments, the electrochemical reactions at cathode 206A generate a cathode effluent stream 206S in cathode effluent flow chamber 206. In some embodiments, cathode effluent stream 206S includes a basic effluent stream 210A. In some embodiments, alkaline effluent stream 106A includes basic effluent stream 210A, as will be discussed in greater detail below. In some embodiments, cathode effluent stream 206S includes a gaseous stream 210G. In some embodiments, alkaline effluent stream 106A includes gaseous stream 210G. In some embodiments, gaseous stream 210G includes hydrogen gas.
As discussed above, electrochemical reactions at anode 204A and cathode 206A generate separate effluent streams (204S and 206S, respectively) which continue to flow through electrolyzer 102 in their respective flow channels, while any generated gaseous products (gaseous streams 208G and 210G) are driven upward by their own buoyancy. In some embodiments, the half reaction occurring at cathode 206A is water reduction, producing hydrogen (H2) as stream 210G and hydroxyls (base, XOH) as 210A. In some embodiments, the half reaction occurring at anode 204A is water oxidation, producing oxygen gas (O2) as 208G and protons (acid, HA) as 208A. In some embodiments, the oxidation half reaction includes a chlorine evolution reaction, resulting in the production of chlorine gas (Cl2) in 208G. In some embodiments, anode effluent flow chamber 204 and cathode effluent flow chamber 206 each include at least one fluid effluent outlet 212 and at least one gas effluent outlet 214 to remove reaction products, e.g., 204S and 206S, from electrolyzer 102. Referring specifically to
In some embodiments, system 100 includes a plurality of electolyzers 102. In some embodiments, electrolyzer 102 includes a plurality of anodes 204A and cathodes 206A. Referring specifically to
In some embodiments, liquid and gaseous product species produced in given effluent chamber may be separated within or outside of electrolyzer 102. Referring now to
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In some embodiments, anode effluent processing unit 108 is a holding container for at least a portion of anode effluent stream 204S. In some embodiments, anode effluent processing unit 108 is configured to process at least a portion of anode effluent stream 204S, e.g., into unit outlet stream 108S. In some embodiments, anode effluent processing unit 108 is in fluid communication with acid effluent stream 208A. In some embodiments, anode effluent processing unit 108 is in fluid communication with gaseous effluent stream 208G. In some embodiments, anode effluent processing unit 108 includes a fuel cell, release unit, sterilization unit, or combinations thereof.
In embodiments where anode effluent processing unit 108 is a fuel cell, an oxidation reaction in electrolyzer 102 produces chlorine gas as a part of anode effluent stream 204S, e.g., gaseous stream 208G. In these embodiments, gaseous stream 210G from cathode effluent stream 206S includes hydrogen gas. Gaseous streams 208G and 210G are each fed to the fuel cell, which produces electricity and hydrochloric acid (HCl) as unit outlet stream 108S. In some embodiments, a portion of the HCl is used to neutralize basic streams evolved elsewhere in system 100, as will be discussed in greater detail below.
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In some embodiments, cathode effluent processing unit 110 is configured to process at least a portion of cathode effluent stream 206S, e.g., into unit outlet stream 110S. In some embodiments, cathode effluent processing unit 110 is in fluid communication with basic effluent stream 210A. In some embodiments, cathode effluent processing unit 110 is in fluid communication with gaseous stream 210G. In some embodiments, cathode effluent processing unit 110 includes a holding tank, capture tank, mixing tank, sterilization unit, or combinations thereof. In some embodiments, cathode effluent processing unit 110 is in fluid communication with a brine inlet stream B, a carbon dioxide inlet stream C, or combinations thereof. In some embodiments, the source of carbon dioxide in the carbon dioxide inlet stream is a flue gas. In some embodiments, cathode effluent processing unit 110 contacts basic effluent stream 210A, e.g., alkaline salt water, with the brine, carbon dioxide, or combinations thereof. Without wishing to be bound by theory, in some embodiments, basic effluent stream 210A causes precipitation of alkali earth metals cations by reaction with hydroxyls to form alkali earth metal hydroxides (M(OH)2, M=Mg2+, Ca2+). These M(OH)2 are of interest as a carbon-free feedstock material for cement manufacturing. In some embodiments, reaction with carbon dioxide from the carbon dioxide stream forms alkali earth metal carbonates M(CO3) instead of M(OH)2.
In some embodiments, system 100 includes a separation unit 112. In some embodiments, separation unit 112 is in fluid communication with cathode effluent processing unit 110 and configured to receive unit outlet stream 110S. In some embodiments, unit outlet stream 110S includes basic effluent stream 210A processed by cathode effluent processing unit 110. In some embodiments, separation unit 112 separates basic effluent stream 210A into at least an alkaline product stream 112A and an alkaline salt water stream 112B. Separation unit 112 can be any suitable separator or series of separators for performing liquid/solid separation techniques, including but not limited to, filtration, hydrocyclone separators, or combinations thereof. In some embodiments, alkaline product stream 112A includes alkali earth metal carbonates, alkali earth metal hydroxides, or combinations thereof. In some embodiments, alkaline product stream 112A is removed from system 100 as a desired product, e.g., for cement manufacturing. In some embodiments, separation unit 112 is in fluid communication with electrolyzer 102. In some embodiments, at least a portion of alkaline salt water stream 112B is recycled in influent stream 104.
In some embodiments, system 100 includes a neutralization unit 114. In some embodiments, neutralization unit 114 is in fluid communication with electrolyzer 102, anode effluent processing unit 108, cathode effluent processing unit 110, separator 112, or combinations thereof. In some embodiments, neutralization unit 114 produces a system effluent stream 114S. In some embodiments, system effluent stream 114S includes concentrated carbon dioxide, demineralized salt water, sterilized salt water, neutralized salt water, or combinations thereof. In some embodiments, at least a portion of system effluent stream 114S, e.g., neutralized salt water, is recycled in influent stream 104.
In some embodiments, neutralization unit 114 combines outlet streams 108S, typically basic, and 110S, typically acidic, to neutralize the two streams. In some embodiments, neutralization unit 114 is fed at least a portion of alkaline salt water stream 112B from separation unit 112. Upon combination in neutralization unit 114 with outlet stream 108S, alkaline salt water stream 112B is neutralized and can be removed from system 100 as demineralized salt water. In some embodiments, neutralization unit 114 is fed basic effluent stream 210A saturated with carbon dioxide by cathode effluent processing unit 110. Upon combination in neutralization unit 114 with outlet stream 108S, saturated basic effluent stream 210A releases concentrated carbon dioxide that can be removed from system 100. The remaining neutralized salt water can then also be removed as a product, or recycled back to electrolyzer 102 in influent stream 104.
As discussed above, in some embodiments, system 100 includes brine inlet stream B. In some embodiments, brine inlet stream B is in fluid communication with electrolyzers 102, anode effluent processing unit 108, cathode effluent processing unit 110, or combinations thereof. Brine inlet stream B is configured to provide brine to system 100 for treatment, e.g., by electrolyzers 102. In some embodiments, brine inlet stream B is pretreated before entering system 100. In some embodiments, brine inlet stream B is pretreated before entering electrolyzers 102, anode effluent processing unit 108, cathode effluent processing unit 110, or combinations thereof.
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By way of example, membrane-less electrolyzers powered by electricity are used to split salt water into acidic and alkaline effluent streams (along with H2/O2 co-products), where the alkaline cathode effluent is used to cause precipitation of alkali earth metals cations by reaction with hydroxyls to form alkali earth metal hydroxides (M(OH)2, M=Mg2+, Ca2+) as the desired product. These M(OH)2 are of interest as a carbon-free feedstock material for cement manufacturing. In some embodiments, a fraction of the alkaline effluent leaving the separation stage is recycled to the electrolyzer, while the rest is sent to a mixing or neutralization vessel where it is mixed with acidic effluent from the electrolyzer to return the water stream to a desired discharge pH. In one embodiment, CO2 is injected into the mixing tank or separation unit(s) to produce alkali earth metal carbonates, e.g., M(CO3) instead of M(OH)2.
Methods and system of the present disclosure are advantageous to provide acid, base, hydrogen gas, and oxygen gas products from salt water (brine) in a durable and cost-effective manner. The system includes an electrolyzer employing porous electrodes to convert aqueous salt solutions (brine) into these valuable products. The systems of the present disclosure are scalable and allow higher concentrations of acid and base products to be produced with built-in structures for separating and collecting gaseous products from the liquid products. Finally, as discussed above, the systems of the present disclosure are advantageous for use in a broad range of applications, including capturing alkali earth metal hydroxides and/or carbonates from seawater, capturing and concentrating carbon dioxide, sterilizing salt water, and simultaneously treating salt water and capturing/concentrating CO2.
Disclosure relevant to the instant application can also be found in the co-owned U.S. patent application Ser. No. 15/269,804, filed Sep. 19, 2016, the content of which is incorporated herein by reference in its entirety.
Although the invention has been described and illustrated with respect to exemplary embodiments thereof, it should be understood by those skilled in the art that the foregoing and various other changes, omissions and additions may be made therein and thereto, without parting from the spirit and scope of the present invention.
This application is a national stage filing of International Patent Application No. PCT/US2020/024699, filed Mar. 25, 2020, claims the benefit of U.S. Provisional Application Nos. 62/823,516, filed Mar. 25, 2019, and 62/993,888, filed Mar. 24, 2020, which are incorporated by reference as if disclosed herein in their entireties.
Filing Document | Filing Date | Country | Kind |
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PCT/US2020/024699 | 3/25/2020 | WO | 00 |
Number | Date | Country | |
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62823516 | Mar 2019 | US | |
62993888 | Mar 2020 | US |