WO2007008591A9 - Methods and apparatus for generating oxidizing agents - Google Patents
Methods and apparatus for generating oxidizing agentsInfo
- Publication number
- WO2007008591A9 WO2007008591A9 PCT/US2006/026338 US2006026338W WO2007008591A9 WO 2007008591 A9 WO2007008591 A9 WO 2007008591A9 US 2006026338 W US2006026338 W US 2006026338W WO 2007008591 A9 WO2007008591 A9 WO 2007008591A9
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- anode
- carbon felt
- aqueous solution
- carbon
- typically
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/467—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction
- C02F1/4672—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction by electrooxydation
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/46104—Devices therefor; Their operating or servicing
- C02F1/46109—Electrodes
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/46104—Devices therefor; Their operating or servicing
- C02F1/46109—Electrodes
- C02F2001/46133—Electrodes characterised by the material
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/306—Pesticides
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/32—Nature of the water, waste water, sewage or sludge to be treated from the food or foodstuff industry, e.g. brewery waste waters
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/32—Nature of the water, waste water, sewage or sludge to be treated from the food or foodstuff industry, e.g. brewery waste waters
- C02F2103/325—Nature of the water, waste water, sewage or sludge to be treated from the food or foodstuff industry, e.g. brewery waste waters from processes relating to the production of wine products
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/4611—Fluid flow
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/46115—Electrolytic cell with membranes or diaphragms
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/4618—Supplying or removing reactants or electrolyte
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/4618—Supplying or removing reactants or electrolyte
- C02F2201/46185—Recycling the cathodic or anodic feed
Definitions
- the field of the invention is devices and methods for electrochemical generation of oxidizing species, especially as they relate to anodic in situ generation of such species in a fluid.
- Oxidative species including ozone, hypochlorite, hydrogen peroxide, persulfate, chlorine dioxide, and hydroxyl radicals are frequently used to sterilize water and destroy toxic organic compounds.
- Oxidative species some exhibit sufficient chemical stability in water to keep the water sterile over relatively long periods, while other oxidative species ⁇ e.g., ozone) have relatively short half lives in water, which potentially allows reinfection of previously sterilized water.
- hypochlorite Ol "
- hypochlorite Ol "
- Hypochlorite is relatively stable, non toxic to humans, and thought to oxidize bacterial cell membranes. Hypochlorite is also known to bleach numerous colored substances, typically by oxidation of aromatic ring structures in the colored substance.
- hypochlorite is also known to react with naturally occurring organic materials, including fulvic and humic acids (e.g., present in soil and sediments in lakes, rivers, and ground water) to form chloromethanes and other toxic byproducts.
- hypochlorite produces a relatively bad taste in the treated water.
- ozone may be employed as a sterilization agent.
- Ozone is chemically more aggressive as a sterilizing agent, but is often more expensive and has a relatively short half life in water. Therefore, ozone sterilization typically requires in situ production at the point of use.
- hydrogen peroxide may be employed as a sterilizing agent via photolytic cleavage of the H 2 O 2 to generate the OH radical as active species. While the hydroxyl radical is an even stronger oxidizing agent as compared to ozone, the hydroxyl radical also has the shortest half life in water.
- photolytic hydroxyl radical generation is often limited by turbidity or other compounds that absorb and/or scatter incident light.
- Electrosynthesis Corp. developed a device based on precious metal coated niobium electrodes which was installed in a water stream.
- Diamond coatings are characterized as having very high oxygen overpotentials, which is thought to be a prerequisite for generating hydroxyl radicals and/or oxidizing organic materials at high efficiency.
- Magneli phase titanium suboxide electrodes have been employed to create a device that was effective as a sterilizing device in contaminated waters (Magneli phase titanium oxide is characterized by its high oxygen overvoltage).
- Electrode materials are either often relatively expensive, difficult to replace by an inexperienced user, and/or typically require relatively large amounts of energy to provide efficient sterilization/decontamination.
- the present invention is directed to various devices and methods of electrochemical generation of oxidative species in an aqueous solution having typically neutral pH using a carbon felt flow-through anode under conditions that reduce, and more typically eliminate oxidative damage to the anode while generating the oxidative species in an amount effective to reduce and/or destroy a contaminant.
- a method of treating an aqueous solution in which an electrolytic cell is provide having an anode in an anode compartment, a cathode in a cathode compartment, and a diaphragm separating the anode compartment from the cathode compartment.
- the anode comprises a carbon felt that is conductively coupled to an electrical connector such that a flow path is formed to allow flow of the aqueous solution through the carbon felt.
- the aqueous solution is moved through the anode compartment such that substantially the entire solution passes through the carbon felt from one side to another side, and in yet another step, the electrolytic cell is operated at a current density effective to generate oxidative species in an amount sufficient to oxidize a contaminant in the aqueous solution.
- the carbon felt is prepared from carbonized organic textile fibrous felts and has a surface area of about 0.1-5 m 2 /g to about 1200 m 2 /g and even higher (where the carbon felt is activated). While the exact configuration is of the carbon felt may be variable, it is typically preferred that the carbon felt configuration will allow for a flow path having a length of between 0.1 cm and 10 cm, and even more preferably between 0.5 cm and 5 cm.
- Suitable aqueous solutions will have an approximately neutral pH of between 5.5 and 8.5, and more typically between 6.5 and 7.5, and pass through the carbon felt at a flow rate of 0.1 ⁇ 7cm 3 *min to 10 ml/cm 3 *min, and more preferably at a flow rate of 0.5 ml/cm 3 *min to 3 ml/cm 3 *min.
- the oxidative species may vary considerably. However, preferred oxidative species include ozone, hydrogen peroxide, hydroxy radicals, oxygen ions, singlet oxygen, and superoxide anions.
- the contaminant in the aqueous solution may vary from source to source, and suitable contaminants include bacteria, spores, viruses, eukaryotic cells and fragments of thereof, optionally halogenated aromatic organic compounds, and dyes. Where desirable, it is also contemplated to recycle at least part of the aqueous solution back to the anode compartment after the solution has passed through the carbon felt.
- Preferred current densities are typically between 10 mA/cm 2 and 500 mA/cm 2 , and more preferably between 30 mA/cm 2 and 100 mA/cm 2 , and it should be noted that the cell can be continuously operated under such conditions for at least 6 hours, more typically at least 24 hours, and most typically at least 48 hours without apparent oxidative damage (visual inspection using 2Ox optical magnification) to the carbon felt anode.
- Figure 2 is a schematic view of another exemplary device according to the inventive subject matter.
- high-surface area carbon felts provide for highly effective in situ flow-through anodes for sterilization and chemical decontamination, especially when operated in substantially neutral (pH of between about 5.5 and 8.5) aqueous streams. Most typically, sterilization and chemical decontamination is achieved by production of oxidizing species rather than by direct anodic oxidation of the contaminants. Remarkably, the high-surface area carbon felts remained undegraded, even at current densities ordinarily expected to destroy the carbon felt anode to carbon dioxide.
- the carbon anode is substantially completely covered by a protective mixed crystal coating consisting essentially of ruthenium oxide and titanium oxide (Reger et al. describe and depict oxidative destruction of uncoated materials as comparative examples). Still other carbonaceous electrodes are described in, for example, U.S. Pat. Nos.
- the anode in all known carbonaceous anodes, the anode is only used as a 'static electrode' that is in contact with the anolyte.
- the electrolyte is in substantially non-moving contact with the internal surfaces of the porous or otherwise high-surface anode and thus subject to oxidation of locally generated oxidative species, especially where the anode is operated at conditions that promote formation of such oxidative species.
- the inventors contemplate that by continuously passing the anolyte through the entire volume (including the internal surfaces) of the anode, oxidative damage from oxidative species to the anode is avoided as the oxidative species either react with a passing contaminant in the electrolyte, are removed from direct contact with the anode by the moving anolyte, and/or otherwise decay due to their chemical instability.
- the oxidizing species may be 'washed off the anode before reaching residence time and quantities sufficient to damage the anode.
- carbon felt refers to a textile material that predominantly comprises randomly oriented and intertwined carbon fibers, which are typically fabricated by carbonization of organic felts (see e.g. , IUPAC Compendium of Chemical Terminology 2nd Edition (1997)). Most typically, organic textile fibrous felts are subjected to pyrolysis at a temperature of at least 1200 0 K, more typically 1400 0 K, and most typically 1600 0 K in an inert atmosphere, resulting in a carbon content of the residue 90 wt%, more typically 95 wt%, and most typically 99 wt%.
- contemplated carbon felts will have a surface area of at least about 0.01-100 m 2 /g, and more typically 0.1-5 m 2 /g, most typically 0.3-3 mVg, and where the carbon felt is activated, will have a surface area (BET) of more than 100-500 m /g, more typically at least about 500-800 m /g, even more typically at least about 800-1200 m /g, and most typically at least about 1200-1500 m 2 /g, or even more.
- the carbon felt may be graphitic, amorphous, have partial diamond structures (added or formed by carbonization), or a mixture thereof.
- the monopolar parallel plate reactor 100 includes a pair of backing plates 102 that confine the plastic cell body panels 104, typically including one or more flow channels for feeding and/or circulating anolyte or catholyte to the respective anode and cathode compartments 110 and 120, respectively.
- Anolyte and catholyte ports 106 and 108 are fluidly coupled to the body panels to deliver the electrolyte to the respective compartments.
- the anode compartment includes the carbon felt anode 112 that is conductively coupled to the electrical connector 114.
- the connector has a grid shape or otherwise provides openings such that anolyte flowing from the panel 104 passes through the connector 114 and carbon felt anode 112 into the cell gap 130.
- Treated anolyte that has flown through the carbon felt anode 112 is then withdrawn from the anode compartment through a port (not shown) and recirculated for a desirable number of passes.
- the arrows indicate the direction of flow of the anolyte and catholyte. Feeding the anolyte that is to be treated is typically performed from a tank or other reservoir (not shown), but may also be implemented by direct feed from a process.
- the diaphragm 132 that defines the boundary of the cathode and anode compartments in the electrolyte.
- Cathode 122 is typically mechanically coupled to body panel 104 to complete the electrochemical cell.
- the catholyte may be circulated through the cathode compartment, which may include a porous or otherwise open-structured cathode to permit catholyte flow through the cathode.
- the cell may also be constructed as a flow through cell in which the solution to be treated enters the anode compartment and exits the cathode compartment.
- the term "flow through” means that the anolyte enters one side of the anode at a flow rate and exits the anode at that flow rate on another side, typically traversing the entire cross section of the anode.
- substantially the entire volume (i.e., greater than 90 vol%, more typically greater than 95 vol%, even more typically greater 99 vol%) of anolyte to be treated will enter the anode on one side and pass through a volume of the anode and exit on the other side.
- cells with a flow-through anode will typically have an anolyte feed port on one side of the anode and an anolyte withdrawal port on the other side of the anode.
- the anolyte may also be withdrawn from the cathode compartment (e.g., where the anolyte is in at least temporary fluid communication with the catholyte).
- suitable electrolytic cells may be configured as monopolar cells or bipolar cells, each or which may be stacked or configured independently of each other.
- the cell includes a body panel on at least the anode side that is configured such that anolyte is (preferably fed into the body panel and) evenly distributed over one side of the anode.
- the anolyte may be fed in a continuous flow to the anode compartment or in batches. Where the flow to the anode compartment is discontinuous, it is generally preferred that the anolyte is circulated within the anode compartment such that the anolyte flows through the anode.
- Suitable containers may have various volumes, and it is generally contemplated that the container (which at least partially encloses the anode and cathode) will have a volume of between about 50 ml to several 100 liters (and even more). Among other things, it should be recognized that the volume of a container will be determined by the volume flow of the solution, the concentration of the contaminant, and the current/voltage applied to the electrodes.
- the anolyte and the catholyte may be provided to the electrolytic cell in all known manners. Thus, continuous and discontinuous flow are both deemed appropriate. Where desired, at least one of the anolyte and catholyte may also be circulated. However, it is preferred that during operation at least the anolyte will substantially continuously (e.g., at least 90% of the time, and more typically at least 95% of the time) flow through the anode. It should be appreciated that the electrolytes may be moved using any manners known in the art.
- the electrolytes are pumped at a predetermined flow rate, wherein the electrolyte may be pumped from a reservoir or directly from a process operation (e.g., dying bath, rinsing bath, etc.). Alternatively, at least one of the electrolytes may also be moved by gravity.
- a process operation e.g., dying bath, rinsing bath, etc.
- the flow rate of the anolyte through the anode and/or anode compartment may vary considerably and will typically depend on various factors, including the concentration of the contaminant, total anode surface, conductivity of the anolyte, and current density. However, it is generally preferred that the anolyte will pass through the anode at a flow rate of between about 0.01 ml/cm 3 *min to about 100 ml/cm 3 *min, more preferably between about 0.1 ml/cm 3 *min to about 10 ml/cm 3 *min, and most preferably between about 0.5 ml/cm 3 *min to about 3 ml/cm 3 *min (cm 3 reflects bulk volume of carbon felt anode) where the anode is operated under conditions that allow formation of oxidative species.
- the anolyte is preferably fed to one side of the anode via a distributor structure, which may be integral to the body panel, or may be a dedicated distribution device. Once the anolyte exits the anode, it is contemplated that all manners of withdrawing the anolyte from the anode compartment are deemed suitable for use herein.
- treated anolyte can be removed from the anolyte compartment using one or more fluid ports that are configured to receive the treated anolyte in a continuous or intermittent manner. The treated anolyte may then be recirculated to the anode for further treatment, stored in a tank, or can be discharged.
- the flow rate of the catholyte will be determined at least in part by the current density, conductivity, gap width, and other factors that are well within the scope of the person of ordinary skill in the art.
- the flow rate for the catholyte will be between 0.01 vol% (of the total cathode compartment volume) per hour and 50 vol% per hour (or even more), more typically between 0.1 vol% per hour and 20 vol% per hour, and most typically between 0.5 vol% per hour and 10 vol% per hour.
- circulation of the catholyte may not be needed or may only be temporary. With respect to feeding and withdrawing the catholyte, the same considerations as for the anolyte apply.
- the anode material comprises carbon felt produced from an organic textile material via carbonization (see above).
- the carbon felt will have a thickness of between about 0.1 cm and 10 cm (and in some cases even more), and even more preferably between about 0.5 cm and 5 cm, while the width and length are generally dependent on the particular electrolytic cell configuration.
- appropriate anode thicknesses and material parameters will at least in part be determined by the backpressure generated by the anode and desired flow rate.
- anode is fabricated from porous carbonaceous materials, including glassy carbon and similar materials so long as such materials allow anolyte flow through the carbonaceous material (e.g., via network of interconnecting pores or channels) at a rate sufficient to reduce or even eliminate oxidative carbon degradation when the anode is operated under conditions that generate oxidative species.
- Suitable alternative anode materials include fabrics/webbings that include activated carbon fibers, graphite felt, and any reasonable combination thereof.
- Still further contemplated anode materials also include composite materials that include the felt or other carbonaceous materials.
- suitable anodes may be manufactured from a conductive polymer that is coated, or in which is embedded carbon felt or other carbonaceous materials.
- cathodes may vary substantially, and a particular choice for the cathode material and configuration will typically depend on the particular solution and/or contaminant that is to be treated.
- appropriate cathode materials are electrochemically relatively inert. Therefore, especially preferred cathode materials include platinum-coated titanium.
- numerous other metals, metal alloys, and even carbon are considered suitable for use herein.
- the cathode material and configuration may be identical with the anode material and configuration.
- the cathode may have numerous configurations, and may include materials and configurations in which the solution can pass through the cathode, as well as impermeable materials and configurations.
- the anolyte that includes the contaminant is an aqueous solution having a substantially neutral pH, typically between about 5.5 and 8.5, more typically between about 6.0 and 8.0, and most typically between about 6.5 and 7.5).
- more alkaline or more acidic solutions may also be desired, especially where the so desired pH will increase solubility of the contaminant or oxidation product(s) of the contaminant.
- anolytes need not be restricted to purely aqueous solutions, and non-aqueous solutions are also expressly contemplated, including those comprising emulsifiers, organic solvents, and even liquefied gases.
- generally preferred solutions especially include waste streams form an industrial process, wherein such solutions are either circulated between the process and the electrochemical cell (which may further include use of a reservoir), or be directly fed from the process to the electrolytic cell.
- Exemplary processes and sources include rinsing or washing operations (e.g., from fruit or animal processing plant, or from metal plating operations), sterilization, cooling/heating water, aqueous solvents for chemical (e.g., chromatography supplies, buffers, etc.) and/or biological processes (e.g., fermentations, enzymatic reactions, etc.).
- rinsing or washing operations e.g., from fruit or animal processing plant, or from metal plating operations
- sterilization e.g., from fruit or animal processing plant, or from metal plating operations
- cooling/heating water e.g., aqueous solvents for chemical (e.g., chromatography supplies, buffers, etc.) and/or biological processes (e.g., fermentations, enzymatic reactions, etc.).
- aqueous solvents for chemical e.g., chromatography supplies, buffers, etc.
- biological processes e.g., fermentations, enzymatic reactions, etc.
- a contaminant may vary substantially.
- contemplated contaminants include bacteria (including spores), viruses, eukaryotic cells, halogenated (typically aromatic) organic compounds, dyes or otherwise colored compounds, and all organic matter directly or indirectly derived from contact of the organic matter with water. Therefore, it should be recognized that the pH of suitable solutions may vary, and it is generally preferred that electrolysis according to the inventive subject matter will be in the neutral pH range. Suitable pH values may be adjusted by adding acid or base, or a buffer system to the anolyte.
- the solution may further be modified to increase and/or decrease conductivity. Where conductivity is increased, all known salts (preferably with insignificant interference [e.g., electroplating] to the electrolytic process) are considered suitable herein. Similarly, the solution may also be diluted, or otherwise reduced in conductivity (e.g., precipitation, chemical modification, or filtration of conductive species in the solution).
- the current and/or voltage of contemplated systems will vary substantially, and all currents and/or voltages suitable for reduction of the contaminant are considered appropriate for use herein.
- typical voltages will be in the range of 0-100 Volt, and more typically between 10 Volt and 50 Volt, at currents of between about 1 mA (or even less) and 100 A and higher, and more typically between about 0.1 A and 10 A.
- current densities will preferably be in the range of about 1 mA/cm 2 and 1000 mA/cm 2 , more preferably between about 10 mA/cm 2 and 500 mA/cm 2 , and most typically between about 30 mA/cm 2 and 100 mA/cm 2 .
- the term "about” in conjunction with a numeral refers to a range of that numeral starting from 10% below the absolute of the numeral to 10% above the absolute of the numeral, inclusive.
- the term “about 10 mA/cm 2 " refers to a range of 9 mA/cm 2 to 11 mA/cm 2 .
- the contaminant may be oxidized directly at the anode, or indirectly via an oxidative species.
- the current density will be adjusted such that oxidative species are formed in the particular anolyte.
- preferred species include ozone, hydrogen peroxide, hydroxy radicals, oxygen ions, superoxide anions, singlet oxygen, etc. It is contemplated that formation of such oxidative species will provide for reactive molecules that then oxidize the contaminant.
- the contaminant is predominantly oxidized ⁇ i.e., at least 51% of the contaminants, more typically at least 70% of the contaminants, and most typically 85-90% of the contaminants) via such reactive species produced from the aqueous solution rather than being directly oxidized on the anode.
- the inventors performed numerous experiments to generate oxidative species, and in some cases to also perform direct oxidation of various compounds. While generation of oxygen was relatively simple to observe, the detection of hydroxyl radicals, ozone, peroxide, and other oxidative species typically requires expensive and sophisticated equipment. Therefore, the inventors decided to indirectly detect oxidative species by adding materials to the water that react with or capture these species. Initially it was believed that small amounts of chloride ions were being converted to hypochlorite, which could act as the oxidizing agent. However, subsequent experiments with de-ionized water conclusively demonstrated that hypochlorite was not formed in an amount sufficient to react with oxidizable molecules. Instead, it was found that all or almost all of the contemplated configurations and methods allowed for the generation of reactive species that indirectly oxidized contaminants. In some cases, direct oxidation of the contaminant was also observed.
- carbon felt materials made from dehydrogenation of long chain organic structures remained intact, even when continuously operated for prolonged periods (e.g., more than 2 hours, more typically more than 6 hours, even more typically more than 24 hours, and most typically more than 48 hours) at currents of 50 mA/cm 2 (cm 2 representing the gross dimensions of anode felt portion, not actual surface area), which indicates that oxygen and other oxidizing species were generated at higher overpotentials than carbon dioxide formation from the carbon at the electrodes.
- certain carbon black and graphitic structures were oxidized at significant rates (especially where no flow-through configuration was implemented).
- An electrochemical cell was constructed as a monopolar parallel plate reactor similar to the device of Figure 1.
- the anode was made by attaching a carbon felt pad to a predrilled graphite feeder plate.
- the carbon felt was 10 cm by 4 cm, and 1 cm thick.
- the cathode was a flat titanium plate coated with platinum.
- the cell gap (distance between carbon felt and the cathode) was 14 mm.
- the flow through the cell was arranged so that the treated water flowed out of the top of the cell after flowing through the felt in the anode compartment.
- the flow rate was adjusted to 30 ml/min to correspond with a once through treatment which removed the color and odor from the water in the exiting stream.
- the water was dosed with 2 g/liter of sodium sulfate to increase the conductivity.
- the experiments were conducted at room temperature. The water was first pumped through the anode compartment with the current off and samples taken to check for concentrations of the target contaminant. This ensured that the inventors would not observe effects based on adsorption onto the high surface area felt.
- a constant current of 3.0 A was used at various voltages, depending on the particular experiment. Typical voltages were about 12 volts, with the actual voltage being predominantly determined by the cell gap and electrolyte conductivity.
- Acid violet 7B a common triphenylene dye identified by reference to the Color Index as number 42745 was added to deionized water at a concentration of 100 milligrams per liter. Deionized water was made conductive with addition of 2 grams per liter of sodium sulfate. This solution was pumped through the anode compartment described above with the current off. The dye concentration remained the same. A 3.0 amps current was then applied to the cell and the solution pumped through at the rate of 30 ml per minute. Remarkably, the solution was completely decolorized as it exited the cell. The experiment was repeated with Allura Red AC, a common foodstuff dye identified as CI # 16035, and later with Brilliant Green #42040 in the Color Index with the same results.
- PCB Perchlorobiphenyl
- DDT (l,l-Bis-(p-chlorophenyl)-2,2,2-trichloroethane) extracted from an old disused spray containing the organophosphate pesticide Methidathion (O,O-Dimethyl S-(5-methoxy- l,3,4-thiadiazolinyl-3-methyl)dithiophosphate) was added to the test solution producing a solution which on analysis gave 53 ppm of DDT. After passing through the anode compartment without electrolysis, the concentration was found to be 54 ppm, while no DDT was detected and after electrolysis of the solution in the electrolytic anode compartment.
- sodium sulfate (2 grams per liter) was added as a current carrier. The cell was run at 3 amps, and the resultant treated liquors became clear on standing for 30 minutes with brown sediment of insoluble oxidized organics at the bottom of the liquors. There was no odor from the treated liquors either immediately after treatment or after 4 weeks. It should be noted that the addition rate of sodium sulfate could be lessened or entirely omitted by closer spacing of the electrodes.
- contemplated devices and methods may be employed for the (preferably continuous) sterilization of the effluent from septic tanks without the many problems otherwise associated with hypochlorite handling.
- the devices and methods according to the inventive subject matter may also be employed for self cleaning swimming pool water sterilizers in which both the anode and cathode are made from carbon felt and are electrochemically reversed to inhibit growth of calcium salts on the cathode.
Abstract
Description
Claims
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AU2006269410A AU2006269410B2 (en) | 2005-07-07 | 2006-07-07 | Methods and apparatus for generating oxidizing agents |
US11/994,967 US20090152123A1 (en) | 2005-07-07 | 2006-07-07 | Methods and Apparatus for Generating Oxidizing Agents |
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US60/697,455 | 2005-07-07 |
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WO2007008591A2 WO2007008591A2 (en) | 2007-01-18 |
WO2007008591A3 WO2007008591A3 (en) | 2007-05-03 |
WO2007008591A9 true WO2007008591A9 (en) | 2007-06-14 |
WO2007008591B1 WO2007008591B1 (en) | 2007-08-02 |
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DE102007033445A1 (en) * | 2007-07-18 | 2009-01-22 | Monopharm Handelsgesellschaft Mbh | Diaphragmalyse method and use of the products obtained by the method |
US20130029016A1 (en) * | 2010-04-22 | 2013-01-31 | Koninklijke Philips Electronics N.V. | Beverage carbonator and method for producing such carbonated beverage |
CA3048786C (en) | 2010-09-24 | 2020-11-03 | Dnv Gl As | Method and apparatus for the electrochemical reduction of carbon dioxide |
ES2652601T3 (en) * | 2010-12-03 | 2018-02-05 | Electrolytic Ozone Inc. | Electrolytic cell for ozone production |
CN102745794B (en) * | 2011-04-21 | 2015-01-21 | 北京市自来水集团有限责任公司 | Drinking water electrochemical preoxidation device and method |
WO2012166997A2 (en) | 2011-05-31 | 2012-12-06 | Clean Chemistry, Llc | Electrochemical reactor and process |
CA2851240C (en) * | 2011-10-07 | 2020-10-27 | Robert Brian Dopp | Electrochemical digestion of organic molecules |
US20170107128A1 (en) * | 2012-09-07 | 2017-04-20 | Clean Chemistry, Inc. | System and method for generation of reactive oxygen species and applications thereof |
WO2014136063A2 (en) * | 2013-03-06 | 2014-09-12 | Krupakar Murali Subramanian | Systems and methods for generating and collecting reactive species |
US10259729B2 (en) | 2014-09-04 | 2019-04-16 | Clean Chemistry, Inc. | Systems and method of water treatment utilizing reactive oxygen species and applications thereof |
US10450667B2 (en) | 2014-10-27 | 2019-10-22 | International Business Machines Corporation | System for treating solution for use in electroplating application and method for treating solution for use in electroplating application |
WO2016126694A1 (en) * | 2015-02-02 | 2016-08-11 | T+Ink, Inc. | A sanitizing product creation system |
CA2981034A1 (en) | 2015-03-26 | 2016-09-29 | Clean Chemistry, Inc. | Systems and methods of reducing a bacteria population in high hydrogen sulfide water |
US10883224B2 (en) | 2015-12-07 | 2021-01-05 | Clean Chemistry, Inc. | Methods of pulp fiber treatment |
EP3386948A4 (en) | 2015-12-07 | 2019-06-12 | Clean Chemistry Inc. | Methods of pulp fiber treatment |
US11136714B2 (en) | 2016-07-25 | 2021-10-05 | Clean Chemistry, Inc. | Methods of optical brightening agent removal |
US11311012B1 (en) | 2017-09-07 | 2022-04-26 | Clean Chemistry, Inc. | Bacterial control in fermentation systems |
US11001864B1 (en) | 2017-09-07 | 2021-05-11 | Clean Chemistry, Inc. | Bacterial control in fermentation systems |
EP3735396A1 (en) * | 2018-03-21 | 2020-11-11 | Innovative Water Care, LLC | Method of removing pesticides from wastewater |
CN109904390A (en) * | 2019-01-28 | 2019-06-18 | 武汉理工大学 | A kind of preparation method of lithium metal/nickel plating carbon cloth composite negative pole |
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US3975246A (en) * | 1973-06-09 | 1976-08-17 | Sachs-Systemtechnik Gmbh | Method of disinfecting water |
US4285831A (en) * | 1976-10-05 | 1981-08-25 | Toho Beslon Co., Ltd. | Process for production of activated carbon fibers |
WO1979000346A1 (en) * | 1977-12-06 | 1979-06-28 | Battelle Memorial Institute | Process and machine for washing and bleaching textile materials |
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US4505797A (en) * | 1983-03-24 | 1985-03-19 | Ionics, Incorporated | Ion-exchange membranes reinforced with non-woven carbon fibers |
SE9302213L (en) * | 1993-06-28 | 1994-12-05 | Eka Nobel Ab | Preparation of polysulfide by electrolysis of white liquor containing sulfide |
CA2144035C (en) * | 1995-03-03 | 2003-01-07 | Barry R. Macdougall | Removal of organics from aqueous solutions |
US5770037A (en) * | 1996-11-21 | 1998-06-23 | Konica Corporation | Water processing method |
US5904832A (en) * | 1996-12-20 | 1999-05-18 | Huron Tech Canada, Inc. | Regeneration of active carbon and polymeric adsorbents |
US6315886B1 (en) * | 1998-12-07 | 2001-11-13 | The Electrosynthesis Company, Inc. | Electrolytic apparatus and methods for purification of aqueous solutions |
EP1170259A1 (en) * | 2000-07-05 | 2002-01-09 | Sony International (Europe) GmbH | Electrochemical apparatus and process for purification of fluids |
EP1438445A2 (en) * | 2001-10-22 | 2004-07-21 | Halox Technologies Corporation | Electrolytic process and apparatus |
US6984303B2 (en) * | 2003-02-25 | 2006-01-10 | Noveon Ip Holdings Corp. | Electrochemical production of dyes using graphite felt electrodes |
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AU2006269410A1 (en) | 2007-01-18 |
US20090152123A1 (en) | 2009-06-18 |
WO2007008591A2 (en) | 2007-01-18 |
WO2007008591B1 (en) | 2007-08-02 |
WO2007008591A3 (en) | 2007-05-03 |
AU2006269410B2 (en) | 2009-07-02 |
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