WO2003053859A1 - Fractional deionization process - Google Patents
Fractional deionization process Download PDFInfo
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- WO2003053859A1 WO2003053859A1 PCT/US2002/041062 US0241062W WO03053859A1 WO 2003053859 A1 WO2003053859 A1 WO 2003053859A1 US 0241062 W US0241062 W US 0241062W WO 03053859 A1 WO03053859 A1 WO 03053859A1
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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
- C02F1/469—Treatment of water, waste water, or sewage by electrochemical methods by electrochemical separation, e.g. by electro-osmosis, electrodialysis, electrophoresis
- C02F1/4693—Treatment of water, waste water, or sewage by electrochemical methods by electrochemical separation, e.g. by electro-osmosis, electrodialysis, electrophoresis electrodialysis
- C02F1/4695—Treatment of water, waste water, or sewage by electrochemical methods by electrochemical separation, e.g. by electro-osmosis, electrodialysis, electrophoresis electrodialysis electrodeionisation
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- 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
- C02F1/469—Treatment of water, waste water, or sewage by electrochemical methods by electrochemical separation, e.g. by electro-osmosis, electrodialysis, electrophoresis
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/42—Electrodialysis; Electro-osmosis ; Electro-ultrafiltration; Membrane capacitive deionization
- B01D61/44—Ion-selective electrodialysis
- B01D61/46—Apparatus therefor
- B01D61/48—Apparatus therefor having one or more compartments filled with ion-exchange material, e.g. electrodeionisation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/42—Electrodialysis; Electro-osmosis ; Electro-ultrafiltration; Membrane capacitive deionization
- B01D61/44—Ion-selective electrodialysis
- B01D61/52—Accessories; Auxiliary operation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J47/00—Ion-exchange processes in general; Apparatus therefor
- B01J47/02—Column or bed processes
- B01J47/06—Column or bed processes during which the ion-exchange material is subjected to a physical treatment, e.g. heat, electric current, irradiation or vibration
- B01J47/08—Column or bed processes during which the ion-exchange material is subjected to a physical treatment, e.g. heat, electric current, irradiation or vibration subjected to a direct electric current
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- 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
- C02F1/001—Processes for the treatment of water whereby the filtration technique is of importance
- C02F1/003—Processes for the treatment of water whereby the filtration technique is of importance using household-type filters for producing potable water, e.g. pitchers, bottles, faucet mounted devices
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- 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
- C02F1/005—Systems or processes based on supernatural or anthroposophic principles, cosmic or terrestrial radiation, geomancy or rhabdomancy
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- 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
- C02F1/4602—Treatment of water, waste water, or sewage by electrochemical methods for prevention or elimination of deposits
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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
- C02F1/68—Treatment of water, waste water, or sewage by addition of specified substances, e.g. trace elements, for ameliorating potable water
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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
- C02F1/42—Treatment of water, waste water, or sewage by ion-exchange
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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
- C02F1/4604—Treatment of water, waste water, or sewage by electrochemical methods for desalination of seawater or brackish water
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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
- C02F1/469—Treatment of water, waste water, or sewage by electrochemical methods by electrochemical separation, e.g. by electro-osmosis, electrodialysis, electrophoresis
- C02F1/4693—Treatment of water, waste water, or sewage by electrochemical methods by electrochemical separation, e.g. by electro-osmosis, electrodialysis, electrophoresis electrodialysis
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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
- C02F11/00—Treatment of sludge; Devices therefor
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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
- C02F2201/4612—Controlling or monitoring
- C02F2201/46125—Electrical variables
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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
- C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
Definitions
- the present invention relates to a novel technique for removal of ionic species from a feed stream without creating any scaling, even at higher levels of inlet water hardness.
- the invention deionizes water using a controlled process system that allows the removal of some ionic components separately from other ionic components without causing any scaling problem in the dilute or concentrate compartment of the cell.
- Such scaling has been the limiting operating condition of preexisting electrodeionization ("EDI") systems and explains the lack of commercial success for such systems.
- EDI electrodeionization
- Ion exchange resin based systems The ion exchange resin adsorbs ionic species at their respective active sites. Once the active sites have been exhausted, the resin can be regenerated by washing the resin with acid or alkali to replace either H + or OH " ions, respectively. This process is called regeneration of resin, and it is the main source for removal of cations and anions from various types of fluids. Demineralizing water is one of the most significant uses of this technology.
- Ion exchange membrane based system Ion exchange membrane based system:
- the ion exchange membranes are made of the same material as resin but work on a different principle.
- an electrical driving force is used to activate the movement of ions present in the water within a chamber of the anion and cation membrane.
- the ions are attracted towards the opposite electrical pole, then they meet the ion selective membrane, which allows selective movement of the ions.
- the cation membrane allows cations to move across the membrane and stops any anion from passing through. Similarly, an anion is allowed to pass through the anion membranes, but cations are prevented from further movement.
- Electro dialysis uses a voltage that is much below the point at which water splitting occurs in water. Electro dialysis has a limitation when it comes to treating water for high purity requirements because of high system resistance and its inability to remove ions like silica .
- EDI system
- EDI is a technology that uses resin for its inherent ion adsorbing property along with the ion exchange membrane system of electrodialysis. EDI utilizes electrodialysis process along with resin as a conducting media introduced between the membranes. Normal EDI works on a very narrow band of feed water quality. The feed water quality required has to be equivalent to the product of reverse osmosis ("RO"), with hardness less than 1000 ppb.
- RO reverse osmosis
- Some prior art teaches use of the RO prior to treatment (U.S. Pat. No. 6,379,518). Because of the inability of RO to provide this quality of feed water, softener also becomes a prerequisite.
- the impurities to be removed include strongly ionized cations, such as sodium and calcium, and strongly ionized anions, such as chloride and sulfate.
- strongly ionized cations such as sodium and calcium
- strongly ionized anions such as chloride and sulfate.
- Sodium and chloride ions have a cleaner removal compared to calcium, because the former ionized species are not chemically inclined to precipitate in EDI.
- Calcium and magnesium are vulnerable to precipitation. Depending on the alkalinity of the system, calcium and magnesium convert to the hydroxide or carbonate form; the hydroxide and carbonate products then tend to precipitate.
- Prior art EDI systems are unable to achieve the necessary hardness tolerance required to prevent scaling. Although such systems claim a maximum hardness tolerance of 1 ppm, the systems have been found vulnerable to scaling even at 1 ppm, limiting the usage of the process. Furthermore, some prior art systems designed to prevent scaling and reduce silica require the use of multiple deionizing apparatus and the addition of harsh chemicals (U.S. Pat. No. 6,398,965), the use of a nonstandard resin (U.S. Pat. No. 6,187,162), or the use of different types of resin in different stacks (U.S. Pat. No. 3,330,750; U.S. Pat. No. 3,149,061, U.S. Pat. No. 6,402,917).
- the present invention is directed toward overcoming one or more of the above-mentioned problems by offering a purification process that may be operated in one or more stacks, does not require the addition of harsh chemicals, and may utilize a uniform resin composition.
- a fractional deionization process for the purification of water using multiple stages of electro-deionization is provided in the current invention. This process may be used to purify water that contains contaminants such as magnesium, calcium, carbon dioxide, and silica; of course, the inventive process is not limited to such uses.
- the fractional deionization process includes treatment of a contaminated feed stream in a first deionization module through which a first voltage is applied.
- this first voltage is calculated to remove strongly ionized species from the feed stream while the system is maintained in a state that is not conducive to "scaling" or precipitation of some ions that might otherwise leave the feed stream at inopportune points in the deionization system.
- the first product stream After the feed stream has passed through the first deionization module it becomes the first product stream. Although strongly ionized contaminant species have been substantially eliminated from the first product stream through operation of the first deionization module, a number of more weakly ionized species may remain.
- the first product stream is therefore introduced into a second deionization module. A second voltage is applied to the second deionization module. Greater than the first voltage, the second voltage is calculated to facilitate removal of more weakly ionized species than were removed in the first module.
- application of a voltage of sufficient strength to remove more weakly ionized species tends to cause scaling of the more strongly ionized species due to creation of an unfavorable pH.
- such strongly ionized species are no longer present after having been removed in the first deionization module. Weakly ionized species may therefore be efficiently removed without fear of scaling. The process therefore becomes more energy efficient.
- the process described is best practiced when the feed stream is introduced with around neutral pH and is maintained at a flow velocity of 100 to 200 cm/minute. Of course, other conditions may be contemplated. Although one embodiment of the invention would have the entire process take place within a single deionization stack modified to allow application of more than one voltage at varying points of the stack, another embodiment would have each step of the process occur in a separate, single-voltage stack.
- the process is not limited to the use of only two discrete deionization modules with two discrete voltages. Rather, any number of deionization modules and voltages may be used, to allow increased differentiation of the ionic species removed at each deionization module. If multiple modules were used, the process could occur in one or more stacks. Unlike prior art systems that require different types of resin in separate stacks, the present invention may use the same type of resin in each stack.
- FIG. 1 Flow pattern in a dilute compartment not packed resulting in the by- passing of the flow and maintaining a continuity of the media for ionic movement
- FIG. 2a and 2b Representations of the two possible scenarios of accelerated water splitting at resin-resin and resin-membrane interfaces
- FIG. 3 Diagram illustrating a possible scenario for ionic movement in the first stage resulting in a lower pH in the first stage reject
- FIG. 4 is an illustration of one embodiment of the instant invention.
- FIG. 5 is a graph tracking silica removal from a product over time.
- FIG. 6 is a graph tracking product quality as a function of resistivity over time.
- FIG. 7 is a graph of product quality expressed as a function of resistivity over time.
- the FDI process of the present invention utilizes salt/ion separation of the ion exchange resin and the ion exchange membrane together with the additional function of water splitting in a controlled, sequential manner. This allows a higher level of hardness to be introduced to the system for purification without danger of scaling.
- the FDI process has been used to remove calcium and silica under successive conditions conducive to each of them. In prior forms of EDI, conditions that are favorable for silica removal also result in hardness removal; however, at higher hardness concentration precipitation occurs at conditions suitable for the removal of silica. Such precipitation is eliminated in this invention.
- the FDI process relates to the selective removal of ionic species under different electrochemical process conditions which creates pH conditions by design favorable to non scaling and keeping the ions in solution within the electrodeionization stack.
- a voltage is applied across the stack, which contains charged media positioned between the membranes. While a lower voltage and the consequent current can remove divalent ions such as Ca 2+ and Mg + , much higher voltages are required to remove difficult ions such as silica.
- divalent ions such as Ca 2+ and Mg 2+ precipitate from the feed stream due to resultant pH. This causes scaling in the stack.
- FDI overcomes this deficiency of the conventional EDI system that has low hardness tolerance. FDI allows generation of resin-regenerating ions and imparts mobility to target the ionic species slated for removal. This permits separation without scaling in the system, even for feed water with a hardness of 5 ppm.
- different voltages are applied across adjacent electrodeionization stacks or in adjacent regions within a single electrodeionization unit. A low voltage is applied across the first stack or part of a stack to remove the hardness. A higher voltage is then applied in the second stack or part of a stack to remove the silica and other difficult ions.
- FDI is, therefore, not susceptible to scale formation due to initial high hardness in the feed water stream, because at the silica removal stage, where pH is alkaline, the feed does not have hardness left to be removed.
- Fractional deionization process has been devised with a concept of improving the hardness tolerance of the system without resulting in any precipitation . This has also been designed with a requirement that there should not be any external chemical dosing to prevent scaling, for example acid need not be added. At the same time the system should be able to deliver the target product quality and silica reduction in an energy efficient manner.
- Certain ionic species e.g. Ca 2+ , Mg 2+ , Na + , Cl " , and sulphates are easier to remove because of their natural affinity to respond to deionization adsorbtion process and their ability to transport themselves within the resin media in the direction of driving force.
- Such ionic species do not need high driving force and can be deionized under milder conditions of DC voltage because of their high mobility within the resin media.
- Certain other species do not exist in readily adsorbable or transportable form and do need modification in their structure to respond to the deionization process.
- Water is known to split above a specific voltage, and extent of splitting can be controlled by controlling the applied voltage and the consequent current.
- the pH of the reject stream can be controlled by extent of application of water splitting and behavior of hydrogen and hydroxyl ions and be made conducive to keeping scaling products in solution. Fractional deionization uses the above mentioned concepts to arrive at the objectives of the design. In a sequential manner, or within the same stack, the focus remains on removing ionic species resulting in scale formation and other monovalent ions by applying minimum possible voltage of 3-5 volts per cell pair, which is just above the water splitting voltage.
- This applied voltage is sufficient to significantly reduce the hardness to less than 0.5 ppm as CaCO 3 .
- silica there is no reduction in silica and there is partial reduction in other ionic species which are detailed later in the examples.
- all the ions responsible for scaling have been fractionally removed without applying high voltage, which is not required for their removal and can cause scaling if it is applied.
- this is achieved by passing feed water through the lower portion of the stack first, which is under the influence of a lower voltage. This part of the stack is called the hardness removal zone. If it is done in a single stack a sample can be drawn from this part of the stack through a sampling point to measure reduction in hardness and test of other parameters.
- the PH in the reject stream here is above 9 and mostly 9 to 10.5. This is because the hydroxyl ions act as carriers for silica and carbon dioxide to the reject stream ,which is probably due to their easier diffusion through the anion resin media. This results in alkaline pH in the reject stream and keeps silica completely in solution. In this process other monovalent anionic and cationic ions are also removed to the expected levels. Silica reduction to an extent of less than 5 and up to 2 ppb is possible in this process without any precipitation. When removal of silica in a same stack is achieved, it happens in top section of the stack that is under the influence of higher voltage . This part is called a silica removal zone. A sample can be separately drawn to analyze conductivity and silica to assess the performance of this part of the stack.
- the reject streams of these two stages are handled separately and kept in a recirculation mode.
- Water splitting is known to happen above a minimum voltage for the system, however, it is accelerated at dissimilar resin-resin and resin membrane interfaces shown in figure 2a and 2b. the following criteria are important in FDI process to control and utilize the water splitting:
- Water splitting happens in a controlled manner so that it can be avoided if it is not required to save energy. This is relevant for first stage of FDI, where the bulk of the reduction can be achieved without any significant water splitting.
- Water splitting happens at specified sites where, in the design , there are higher probabilities of using the H* and OH " ions in regeneration of the relevant sites rather than their recombining or going to a reject stream without any participation or beginning to affect the product pH unfavorably.
- Water splitting happens at sites that are under the influence of heavy mixing and not stagnant to avoid chances of any local precipitation. After working with several combinations of distribution of bipolar surface area in between resin-resin and resin-membrane interfaces, it was observed that FDI performance is best when water splitting is limited to just resin-resin bipolar sites. This enables effective utilization of the water split products in the regeneration process and allows maximization of flux through the media. This also ensures that entire membrane area is available for ionic diffusion limited process especially under higher flux or when low level of silica is expected.
- EXPERIMENTAL DETAILS A series of trials has been conducted, each running for 100 to 700 hours.
- the feed water used had an initial conductivity of 5 ⁇ s cm that was increased until it reached 100 ⁇ s/cm.
- the increase of conductivity was accomplished through the external addition of sodium chloride, sodium bicarbonate, and calcium chloride.
- Study has been done at length with the silica addition in the feed.
- the objective of Experiment-01 was to study the pH profile while simulating different conditions in FDI process with changes in voltage conditions. For each case the effect of voltage and amperage has been recorded for the analysis.
- the stack used was of dilute chamber of 9.5 mm and concentrate chamber of 2.5 mm, with an effective membrane size of 190 mm x 350 mm.
- the bipolar surface area of resin to resin interface used was equivalent to half the available membrane surface area.
- the evaluation was done by differing composition of feed at different voltage and amperage conditions. The data selected below categorizes the voltage and amperage effects.
- the feed contains impurities of cations (sodium and calcium) and anions (chloride, bicarbonates, and dissolved carbon dioxide).
- cations sodium and calcium
- anions chloride, bicarbonates, and dissolved carbon dioxide.
- the feed was recirculated such that the product mixed with the feed.
- the conductivity and the pH of the feed were maintained by the addition of cations and anions, as mentioned above, in their chemical solution extemally to compensate for the ions removed in the reject stream.
- the feed pH was observed at a level between 6 to 6.5, with an occasional rise to 7.
- the voltage applied was between 4 to 6 volts/pair and the amperage consumed was very low, not exceeding 0.25 amps.
- section A has a load of silica not exceeding 1 ppm, and there are no impurities other than sodium, chloride, carbonic acid, bicarbonates, or dissolved CO 2 .
- the section B has the load of calcium not exceeding 1 ppm instead of silica. According to this the anionic load consists of chloride and carbonic acid, whereas the cationic load consists of sodium and calcium ions.
- the concentrated stream conductivity at the inlet is varied from 400 ⁇ s/cm to 700 ⁇ s/cm, except the B-1 data where it is only 200 ⁇ s/cm.
- All the calcium ions are separated in the reject side such that the product received contains no calcium and the reject side is loaded with the calcium ions. There are fewer calcium ions in the feed side than in the reject side. Precipitation in the reject side should be avoided, and to achieve this condition, the reject side pH should be slightly acidic; more H* ions should be transferred along with the cations. Maintaining pH below neutral would be enough to prevent calcium precipitation; any more would be a waste of energy. On the other side, in the feed chamber, basicity needs to be avoided. If the pH of the product is neutral or near neutral, the process would run more smoothly. Because more H + ions are used in the reject side, that many more OH ' ions would find their way into the product after getting consumed , so if the product pH is not neutral, having it at slightly more than 7 would not be detrimental at the outlet point.
- the feed contains both the impurities of anionic ions and cationic ions mentioned in the two cases together, which is a mix of strongly and weakly ionized, the most conducive situations required are contrary to each other.
- the reject pH is suitable if it is acidic in one case and if it is basic in another. The methods to derive the individual conditions are different where operating conditions are different.
- the stack used had the following specifications: Effective membrane dimensions were 190 mm x 350 mm. Dilute chamber thickness of 10 mm and concentrate chamber of 2.0 mm. Resin to resin bipolar surface area equals to the half of the membrane surface area. Deminerahzed water was taken with conductivity of 4 ⁇ s/cm. Calcium hardness was added extemally to give the feed a concentration 5 ppm of CaCO 3 . . Concentrate conductivity was maintained at 200 ⁇ s/cm. Voltage applied was 4 to 5 volts per pair.
- Effective membrane dimensions were 190 mm x 350 mm. Dilute chamber thickness of 10 mm and concentrate chamber of 2.0 mm. Resin to resin bipolar surface area equals to the half of the membrane surface area. Deminerahzed water was taken with conductivity of 4 ⁇ s/cm. Calcium hardness was added extemally to give the feed a concentration 5 ppm of CaCO 3 . . Concentrate conductivity was maintained at 200 ⁇ s/cm. Voltage applied was 4 to 5
- the first stage of the multi-stage fractional deionization system was operated at low voltage and low amperage.
- the product pH was observed to be greater than 8, and the reject pH was as low as 3.6-4.2 Hardness decreased from 6 ppm to less than 1 ppm as CaCO 3 .
- the conductivity and thus the salt reduction in this stage is more than 70%, which is less than we would expect even when the reduction of calcium is more than 85%.
- the OH ' ions generated in the dilute compartment are not mobile and do not migrate to the reject side and find a way out in the product.
- the conversion of carbonic acid to the higher form of bi- carbonate is caused by the OH " ions, which are observed by the rise in the alkalinity of the
- the feed water has impurities of silica and carbonic acid.
- the feed pH is between 6 and 6.5.
- the feed in this stage contains as impurities primarily the weakly ionized species that were not eliminated in the first stage.
- both silica and carbonic acid groups require OH " ions and high energy for ionization and movement.
- the voltage required for the second stage is more than 10 volts/pair.
- the objective in the second stage effect is to eliminate all the residual impurities and obtain a product resistivity of 18 Mega ohms.
- the bed was regenerated and then the addition of a feed stream started that included the silica dosage.
- the stack was run for more than 100 hours.
- the conductivity of the reject in water was maintained at 400 ⁇ s/cm.
- a voltage of between 11 and 17 volts/pair was applied. The voltage and the reject-in conductivity together were responsible to give the amperage consumed on the higher side of more than 2.5 amps.
- the addition was started when on re-circulation the product's continuing resistivity was at least 18 M ⁇ .
- Silica addition was started and maintained at a level of 1000 ppb in the feed.
- the silica level was monitored by the Hack spectrophotometer and was observed to be less than 20 ppb at all operating temperatures between 25 and 40° C. Though the silica content was found to be reduced in the product, the product resistivity started falling from 18 to 17 M ⁇ . Upon ceasing addition of silica, the resistivity rose back to 18 M ⁇ .
- the high voltage state is required because the water contains weakly ionized ions.
- Table 4-B has three sets of readings.
- the modification here was to reduce the amperage at the elevated voltage by reducing the conductivity of reject in stream.
- the conductivity was reduced from 400 to 100 ⁇ s/cm.
- the three sets have small variations of flow conditions.
- the stack was run for more than 50 hours without any deterioration in the quality.
- hardness of more than 5 ppm as CaCO 3 has been tackled in the first stage at a low voltage and ampere condition.
- silica if present, is not removed, and carbonic acid partially converts to the stronger ionic group as bicarbonate, but the bicarbonate is still within the water.
- the product of the first stage when is subjected to the second stage where the voltage and the amperage are different and higher, is stripped of the remaining impurities to give a product of highest purity.
- the two stages can be combined by using different stacks connected in series or by using a specially designed stack that can accommodate two electrical stages. Both the configurations were tried to affirm our results.
- FIG. 4 illustrates one embodiment of the current invention.
- a new stack was designed such that water would flow through a specially made design where it could be subjected to two different voltages in a single path.
- the first half path is subjected to one type of voltage and is the first stage of the fractional deionization system, responsible for removing the strongly charged ion and the hardness.
- the second half is a high voltage area responsible for removal of traces of remaining ionic impurities including weakly charged ions.
- Example-02
- Membrane dimensions 190 mm wide and 350 mm long. Dilute chambers: one and half numbers in each stage. Operating membrane surface area 998 cm 2 in each stage.
- the modified two-in-one stack was designed and run as follows: Two separate water circulation loops were made. One feed circulation loop was connected at the inlet of the stack. The water outlet from this stream was the final product, which was put back in the tank for recirculation.
- the feed tank allowed the addition of hardness in the form of calcium chloride and/or sodium chloride and sodium bicarbonate in case the feed conductivity needed to be increased.
- the other loop was of concentrate feed connected to the reject compartment of the stack of both stages. Reject coming out of the stack was diluted to control the concentrate conductivity before being returned to the stream. Initially the stack was started with minimum feed conductivity for several hours so that the stack was set and regenerated. With the relation of membrane surface area mentioned above and given the experience with the standard stack system, the flow rate expected was between 1200 and 1400 cm 3 per minute. The stack was put in operation with following conditions and expectations:
- the stack performance was observed for one of the runs as follows: a) The stack had run initially for 80 hours, including its stabilizing period; b) The feed flow was maintained at 1200 cm 3 per minute and feed conductivity of 12 to 14 ⁇ s/cm, for next 40 hours. (See Table 5, below); c) The feed conductivity was raised to 60 ⁇ s/cm by the addition of sodium chloride, keeping the hardness load of 5 ppm in the feed from 41 hours onwards.
- the hardness and conductivity were measured along with pH of each stream. The result reflects the following: i. The hardness in the feed was 5 ⁇ 1 ppm, whereas the rejection in the first stage was only 90% of that and never crossed 0.5 ppm. The final product was analyzed as less than 24 ppb of hardness. ii. The hardness was also measured in the reject stream, which is the carrier of the removed salts for finding the material balance, and was found to be correct. iii. The pH of the reject of stage-1 was found to be acidic, confirming that the salts removed would not precipitate in the compartment. The pH for the reject of stage- 2was maintained as alkaline, confirming the theory of ions splitting at the higher voltage required for the removal of the weakly charged remaining ions. iv. The product resistivity was maintained between 16 and 13 M ⁇ cm. The major separation having taken place in the first stage and in the absence of any conducting material being supplied in the second stage, the resistivity varied from
- the stack was put in operation with following conditions, 1) Feed conductivity: 15 to 20 ⁇ s/cm.
- the direct current applied in the primary stage was equal to 3 to 5 volts/pair, while the voltage applied in the final stage was in the range of 15 to 18 volts/pair.
- Continuous monitoring was carried out for hardness leakage, residual silica, and resistivity of the product.
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- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Electrochemistry (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
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Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003554580A JP2005512794A (en) | 2001-12-20 | 2002-12-19 | Separation deionization treatment |
CA2470633A CA2470633C (en) | 2001-12-20 | 2002-12-19 | Fractional deionization process |
EP02794360.4A EP1456132B1 (en) | 2001-12-20 | 2002-12-19 | Fractional deionization process |
MXPA04005925A MXPA04005925A (en) | 2001-12-20 | 2002-12-19 | Fractional deionization process. |
AU2002359797A AU2002359797B2 (en) | 2001-12-20 | 2002-12-19 | Fractional deionization process |
KR1020047009527A KR100764937B1 (en) | 2001-12-20 | 2002-12-19 | Fractional deionization process |
Applications Claiming Priority (2)
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US34332301P | 2001-12-20 | 2001-12-20 | |
US60/343,323 | 2001-12-20 |
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WO2003053859A1 true WO2003053859A1 (en) | 2003-07-03 |
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---|---|---|---|
PCT/US2002/041062 WO2003053859A1 (en) | 2001-12-20 | 2002-12-19 | Fractional deionization process |
Country Status (9)
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US (2) | US6896814B2 (en) |
EP (1) | EP1456132B1 (en) |
JP (1) | JP2005512794A (en) |
KR (1) | KR100764937B1 (en) |
CN (2) | CN101070200A (en) |
AU (1) | AU2002359797B2 (en) |
CA (1) | CA2470633C (en) |
MX (1) | MXPA04005925A (en) |
WO (1) | WO2003053859A1 (en) |
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- 2002-12-19 JP JP2003554580A patent/JP2005512794A/en active Pending
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Also Published As
Publication number | Publication date |
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AU2002359797A1 (en) | 2003-07-09 |
KR20040086244A (en) | 2004-10-08 |
US20030201235A1 (en) | 2003-10-30 |
US20050121397A1 (en) | 2005-06-09 |
AU2002359797B2 (en) | 2008-01-31 |
US7338600B2 (en) | 2008-03-04 |
MXPA04005925A (en) | 2005-03-31 |
US6896814B2 (en) | 2005-05-24 |
CN1615273A (en) | 2005-05-11 |
CA2470633A1 (en) | 2003-07-03 |
CN1328180C (en) | 2007-07-25 |
JP2005512794A (en) | 2005-05-12 |
EP1456132A4 (en) | 2009-07-01 |
CA2470633C (en) | 2010-11-09 |
KR100764937B1 (en) | 2007-10-08 |
EP1456132A1 (en) | 2004-09-15 |
CN101070200A (en) | 2007-11-14 |
EP1456132B1 (en) | 2014-01-22 |
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