NZ750562B2 - Use of electrochemical oxidation for treatment of per-and polyfluoroalkyl substances (pfas) in waste generated from sorbent and resin regeneration processes - Google Patents

Abstract

Perfluorinated and polyfluorinated compounds in an effluent stream are destroyed by means of electro-oxidation. Although electro-oxidation can be used to directly treat effluent, a more efficient use is to pre-concentrate applicable pollutants with filters or sorbents. Concentrated perfluorinated and polyfluorinated compounds are removed from the filter or sorbent with a regenerant solution and treated by electro-oxidation. A current density of 0.5 mA/cm2or 1 mA/cm2effectively reduces the level of perfluorinated contaminants within 1-3 hr. using a titanium electrode. This allows both the regenerant and filter or sorbent to be reused and greatly reduces the amount of material that must be treated as hazardous waste. d polyfluorinated compounds are removed from the filter or sorbent with a regenerant solution and treated by electro-oxidation. A current density of 0.5 mA/cm2or 1 mA/cm2effectively reduces the level of perfluorinated contaminants within 1-3 hr. using a titanium electrode. This allows both the regenerant and filter or sorbent to be reused and greatly reduces the amount of material that must be treated as hazardous waste.

Description

Use of Electrochemical Oxidation for Treatment of Per- and Polyfluoroalkyl Substances [PFAS] in Waste Generated from Sorbent and Resin Regeneration Processes Cross-reference to Prior Applications The current application is based on and claims the priority and benefit of United States Provisional ation No. 62/393,389, filed on 12 September 2016.

US. Government Support Not Applicable Background of the Invention Area of the Art The t invention is in the art of pollution control and more specifically is sed to a proves for destroying fluorinated compounds in an aqueous waste .

Description of the Background Art id="p-1" id="p-1" id="p-1"

[0001] Per— and polyfluoroalkyl substances (PFAS) are organic compounds consisting of fluorine, carbon and heteroatoms such as oxygen, nitrogen and . The hydrophobicity of fluorocarbons and extreme electronegativity of fluorine give these and similar compounds unusual properties. Initially many of these compounds were used as gases in fabrication of integrated circuits. The ozone destroying properties of these molecules restricted their use and resulted in methods to prevent their release into the here. But other PFAS such as fluoro—surfactants have become increasingly r. Although used in relatively small amounts, these compounds are readily ed into the environment where their extreme hydrophobicity as well as negligible rates of natural decomposition results in environmental persistence and bioaccumulation. It appears as if even low levels of bioaccumulation may lead to s health uences for contaminated animals such as human beings, the young being especially susceptible. The environmental effects of these nds on plants and microbes are as yet largely unknown. Nevertheless, serious efforts to limit the environmental release of PFAS are now commencing.

Sorption or filtration technologies have been commonly used to separate PFAS from impacted water (including waste water, surface water, drinking water and groundwater). The tion via sorbents or filters relies on sorption and other physical mechanisms that remove PFAS from water. The sorbents or filters (including ion exchange resin, reverse osmosis filters and activated carbon s) will eventually become loaded with high concentrations of PFAS requiring regeneration of the sorbents or filters if they cannot be safely discharged or disposed of by other means. Such regeneration lly involves the use of chemical reagents to wash or release the PFAS from the "spent" sorbents or filters and results in the generation of a "spent regenerant." In some regeneration processes, "spent regenerants" can be reclaimed for reuse. Following the reclamation s, "still bottoms" or "regeneration wastes" will be generated. This invention applies to coupling a filtration technology with a destruction technology that will destroy PFAS in "spent regenerant", "still bottoms" or "regeneration wastes." id="p-3" id="p-3" id="p-3"

[0003] During the process, low concentrations of PFAS from high-volume impacted water become a low-volume high PFAS concentration waste stream; the PFAS mass is not changed, but the effective concentration is increased. The disposal of concentrated PFAS waste streams is not acceptable or is often rohibitive (e.g., complex hazardous waste management). Therefore, a treatment technology that reduces the PFAS mass in "spent regenerant", "still bottoms" or "regeneration " is needed to ensure removal of PFAS from the environment.

Summary of the Invention The t invention ys PFAS in an effluent stream by means of electrooxidation. gh the electro-oxidation process can be used to directly treat nt, the huge volume of most contaminated effluents makes the use of electro-oxidation very inefficient. The present invention provides a more efficient system by using tional effluent treatment systems to pre-concentrate applicable pollutants with ion exchange resin, activated carbon or similar filtration/sorbent materials. Thereafter the electro-oxidation system is used to reduce the more trated pollutant level in the erant" used to flush the tion/sorbent materials. This allows the regenerant to be reused and greatly reduces the amount of material that must be treated as hazardous waste. Moreover, the size of the electro-oxidation electrodes and the consumption of electricity is greatly reduced as compared to direct o—oxidation of primary effluents.

For electro-oxidation current density of 0.5 mA/cm2 or 1 mA/ cm2 can ively reduce the level of per-fluorinated contaminants within 1-3 hr. using a titanium electrode or similar electrode. The process can operate in a variety of effluents provided a concentration of at least 10 mM salt is present. The effluent can be diluted to control the salt level as WO 97875 2017/051204 necessary. Besides fluorinated organic compounds, other organic compounds that contribute to TOC (total organic carbon) are also oxidized.

Description of the s FIGURE 1 is a m of the process of one embodiment of the invention; id="p-7" id="p-7" id="p-7"

[0007] FIGURE 2 is a graphic representation of the reduction in the level of perfluorinated compounds achieved by the present ion; and FIGURE 3 is a graphic representation of the reduction in the level of perfluorinated compounds achieved by the present invention.

Detailed Description of the Invention id="p-9" id="p-9" id="p-9"

[0009] The following description is provided to enable any person skilled in the art to make and use the invention and sets forth the best modes plated by the inventor of carrying out her invention. Various modifications, however, will remain readily apparent to those skilled in the art, since the general principles of the present invention have been defined herein specifically to provide a method to y perfluorinated compounds in waste streams.

The present invention couples a filtration technology with a destructive technology to remove and destroy and/or reduce the mass of PFAS in effluents. The destructive treatment process allows reuse of treatment effluent for filtration media regeneration or safe discharges and eliminates the need to ship waste offsite for disposal. There are several destructive logies that have been studied at bench scale for PFAS destruction and mineralization. But the inventive s is the first to use electro—oxidative (EO) destructive technology for regeneration waste treatment. For e, EO can effectively degrade PFAS with a proven defluorination process to detoxify and destroy PFAS. The current invention is a new application of this destructive technology (particularly electrochemical oxidation technology) for treatment of concentrated PFAS in a waste stream generated from regeneration of any PFAS filtration technology.

The waste stream (including "spent regenerant", "still bottoms" or "regeneration waste") may contain organic solvents (e.g., methanol), concentrated PFAS, total organic carbon (TOC) in a salt on. Both TOC and PFAS have been demonstrated to be destroyed by the ctive EO process. For ce, the use of titanium de (e.g., Ti4O7)electrode with current density of 0.5 mA/cm2 or 1 mA/ cm2 was able to destroy 100% of perfluorooctanesulfonate (PFOS) which is a fluoro—surfactant typically found spent regenerant. In such systems, an electrode surface area of approximately one square meter can cleanse 50 gallons (189 I) of spent rant (a salt concentration of about 10 mM is typically needed for the E0 reactions) within 1-3 hours. The effluent of this EO process can be ly discharged or returned to the E0 process for additional ent.

Many different electrode combinations can be used in the invention. While the test was conducted with a titanium-based electrode known as "electrode T" (Magnéli phase Titanium sub oxide and mixed Magnéli phase Titanium , other odes as shown in Table 1 are effective. The table demonstrates that preparation and composition of the electrode surface (e.g., nanoparticle es, etc.) have a strong influence on overall defluorination. The rate constants and reaction half-lives of the most effective electrodes do not vary significantly.

Table 1 Electrode Defluorination Rate constant Half—life R2 ratio (%) (k, min'i) (tmi min) Mn02 14.6 0.4 x 10'3 173.2 0.995 Sn02 65.8 2.5 x 10'3 27.7 0.995 modified Sn02 73.7 2.9 x 10'2 23.9 0.999 Pb02 70.5 2.7 x 10'2 25.7 0.997 Ce-Pb02 76.9 3.1 x 10'2 22.4 0.999 modified 92.6 3.9 x 10'2 17.8 0.998 Ce-Pb02 Ebonex (titania 53.9 2.9 x 10'2 23.9 0.997 ceramic) The t invention couples EO with sorbent or filtration technologies that are used to remove PFAS from a waste stream as defined above. Electrode configuration and fluidic configuration will be apparent to one of skill in the art. The process can be performed as a batch reactor mode or continuous flow through in which case various c and geometric parameters can be adjusted to ensure mixing and avoid lamellar flow and other surface effects. The s can also be d out in a batch mode in which case standard mixing devices (impellers, etc.) are used to ensure mixing. id="p-15" id="p-15" id="p-15"

[0015] shows a typical overall water treatment system using ion exchange resin (Lead Contactor 16 and Lag Contactor 18) to remove PFOA, PFOS and similar pollutants.

In normal operation, the influent is stored in holding tank 10 and pumped by a pump 12 through a pre-filter 14 and through a series of two ion exchange resin contactors 16 and 18 2017/051204 and through normally open valve 34 to be released as treated effluent. However, when sampling shows that the effectiveness of the ion exchange contactors is decreasing, they can be rated. Valve 34 is closed and valves 36 and/or 38 are opened while a pump 32 pumps rant from the supply tank 24 through the alternate route 42. This flushes pollutants from the contactors 16 and 18 which flow into a holding tank 20. When the contactors 16 and 18 are sufficiently renewed, the process flow returns to the initial configuration.

During regeneration, spent regenerant moves from the holding tank 20 to the regenerant reclamation tank 22. The reclaimed regenerant flows to the holding tank 24 for reuse as regenerant. "Still bottom" is generated from spent regenerant ation; the "still bottom" moves h the E0 reactor 28 where the E0 takes place. The E0 processed rant can optionally be treated with ion exchange resin 30 and is held in the rant makeup tank 26 where various additives may be added before the regenerant moves to the regenerant supply tank 24 for reuse. The valve 40 can be used to discharge excess volumes of regenerant to waste 34.

As shown in Table 2 below, two "still " samples from the ion exchange regeneration process had an average of 6,810 mg/L TOC, 92 mg/L PFOA and 67.9 mg/L PFOS. (Parts-per—million, 10's, is equivalent to mg/L.) After 17 hours of EO treatment, it was evident that the dark color of the still bottoms faded over time and PFOA and PFOS concentrations decreased sharply with 77.2% PFOA and 96.5% PFOS removed. The results of these experiments are shown graphically in Tab|e2 Parameter Sample 1 Sample 2 PFOA 100.5 ppm 83.5 ppm PFOS 68.6 ppm 67.2 ppm TOC Very high Very high CI' (Chloride) Very high Very high id="p-19" id="p-19" id="p-19"

[0019] For another still bottom sample with relatively lower initial PFOA (15.6 mg/L) and PFOS (25.4 mg/L) concentrations that are more typical in ion exchange resin operation, EO with the Ti4O7 electrode was able to completely remove them to non-detectable levels (detection limits of 33 parts-per—trillion, ‘10'12 for PFOA and 22 parts-per—trillion, 10'12 for PFOS) as shown graphically in This demonstrates that that EO, according to our s, can be used to treat liquid wastes containing low to high PFAS concentrations as well as significant TOC and salt loads.

The following claims are thus to be understood to include what is specifically illustrated and described above, what is conceptually equivalent, what can be obviously substituted and also what essentially orates the essential idea of the invention. Those skilled in the art will appreciate that various adaptations and cations of the just- described preferred embodiment can be configured without departing from the scope of the invention. The illustrated embodiment has been set forth only for the es of example and that should not be taken as limiting the invention. Therefore, it is to be understood that, within the scope of the appended claims, the invention may be practiced other than as ically described herein.

Claims (15)

WHAT IS CLAIMED IS:

1. A process for destroying per- and polyfluoroalkyl substances (PFAS) in an aqueous effluent by electro-oxidation comprising: concentrating the per- and uoroalkyl substances using a filtration or sorbent logy; washing a filter or t from the tion or sorbent technology with a regenerant to te a spent regenerant containing the per- and polyfluoroalkyl substances; providing an electrolytic cell with an anode electrode and a cathode electrode; contacting said regenerant with the anode electrode and the cathode electrode while a current flows between said electrodes, thereby destroying the per- and polyfluoroalkyl substances by electro-oxidation to form a reclaimed regenerant; and reusing the reclaimed regenerant in the filtration or sorbent technology.

2. The s of claim 1, wherein the anode electrode is selected from the group consisting of titanium suboxide, MnO2, SnO2, PbO2, Ce-PbO2 and titania ceramic.

3. The process of claim 1, wherein the aqueous effluent is ed from the group consisting of waste water, surface water, ng water and groundwater.

4. The process of claim 1, wherein the electrolytic cell is operated by ng said cell and filling said cell with new spent regenerant following electro-oxidation.

5. The process of claim 1 wherein the electrolytic cell is operated in a flow through mode.

6. The process of claim 5, wherein the flow through mode is used to y perand polyfluoroalkyl substances in a spent regenerant stream generated by any filtration or sorbent technology, and wherein the spent regenerant stream results from stripping per- and polyfluoroalkyl substances from ion exchange contactors to regenerate ion exchange resin therein, thereby allowing the ion exchange resin to be reused.

7. The process of claim 1, wherein the current flows between the odes with a current density between 0.5 mA/cm2 and 1 mA/cm2.

8. The process of claim 1, wherein the anode electrode comprises a titaniumbased electrode.

9. The process of claim 3, wherein the anode ode comprises titanium suboxide.

10. The s of claim 1, wherein contacting comprises destroying PFOA.

11. The process of claim 1, wherein the electrolytic cell is operated in a batch mode.

12. A water treatment system for destroying per- and polyfluoroalkyl substances (PFAS) in an aqueous effluent by electro-oxidation, the water treatment system comprising: a filtration or sorbent technology for concentrating the per- and polyfluoroalkyl substances; a pump for g regenerant from a supply tank to wash a filter or sorbent from the filter or sorbent technology to generate a spent regenerant containing the perand uoroalkyl substances; and an olytic cell with an anode electrode and a cathode electrode, wherein the anode electrode and the cathode electrode are configured to contact said regenerant while a current flows between the electrodes, thereby destroying the per- and polyfluoroalkyl substances by electro-oxidation to form a reclaimed regenerant, and wherein the reclaimed rant is moved from the electrolytic cell to the supply tank to be reused in the filtration or sorbent technology.

13. The water treatment system of claim 12, n the anode electrode comprises a titanium-based electrode.

14. The water treatment system of claim 13, wherein the anode electrode comprises um suboxide.

15. The water treatment system of claim 12, wherein the current flows between the electrodes with a current density between 0.5 mA/cm2 and 1 mA/cm2.