Water recovery system for use in confined spaces
10179745 ยท 2019-01-15
Assignee
Inventors
Cpc classification
C02F1/68
CHEMISTRY; METALLURGY
C02F1/4674
CHEMISTRY; METALLURGY
C02F2201/46115
CHEMISTRY; METALLURGY
C02F2201/001
CHEMISTRY; METALLURGY
C02F9/00
CHEMISTRY; METALLURGY
C02F2303/22
CHEMISTRY; METALLURGY
C02F1/20
CHEMISTRY; METALLURGY
C02F1/4618
CHEMISTRY; METALLURGY
International classification
B01D61/42
PERFORMING OPERATIONS; TRANSPORTING
C02F1/469
CHEMISTRY; METALLURGY
C02F1/68
CHEMISTRY; METALLURGY
C02F9/00
CHEMISTRY; METALLURGY
C02F1/467
CHEMISTRY; METALLURGY
Abstract
A water recovery system can treat water in a confined space. The wastewater treatment system includes a cation-exchange device in which water to be treated, such as wastewater originating in a space station, water discharged by the human body, water produced by condensing water vapor contained in the air, is directly introduced to a cation-exchange resin and thereby treated by cation exchange; a diamond-electrode electrolysis device in which organic substances, urea, and other nitrogen compounds contained in water discharged from the cation-exchange device are decomposed; a catalytic decomposition device in which the residual organic component is brought into contact with a catalyst to be decomposed; an electrodialysis device in which water discharged from the catalytic decomposition device is treated by electrodialysis to produce desalted water as well as an acid and an alkali; and a mineral adding device in which a mineral is added to the desalted water.
Claims
1. A water recovery system in a confined space, comprising: a cation-exchange device in which wastewater originating in a confined space is treated by cation exchange with a Na-type weakly acidic cation-exchange resin; an organic-component decomposing device in which an organic component contained in water discharged from the cation-exchange device is decomposed, comprising a diamond-electrode electrolysis device including conductive diamond serving as an electrode, and a catalytic decomposition device; an electrodialysis device in which water discharged from the organic-component decomposing device is treated by electrodialysis, thereby producing an acid and an alkali; a regeneration unit in which the cation-exchange resin is regenerated using the acid and the alkali produced in the electrodialysis device; a mineral adding unit in which a mineral component is added to a treated water discharged from the electrodialysis device; a first tank that stores the acid and supplies the acid to the cation-exchange device to regenerate the cation-exchange resin; and a second tank that stores the alkali and supplies the alkali to the cation-exchange device to regenerate the cation-exchange resin.
2. The water recovery system according to claim 1, wherein the wastewater is urine, which is treated by the cation-exchange device, and condensed water produced by condensing water vapor contained in air in the confined space is merged into the water from the cation-exchange device prior to the organic component is decomposed.
3. The water recovery system according to claim 1, wherein electrodialysis device comprises an anode, a cathode, and an acid compartment, an anion-exchange membrane, a desalting compartment, a cation-exchange membrane, a bipolar membrane, another acid compartment, another anion-exchange membrane, another desalting compartment, and another cation-exchange membrane disposed in order between the anode and the cathode.
4. A combination, comprising: a confined space; and a water recovery system in the confined space, wherein the water recovery system comprises a cation-exchange device in which wastewater originating in the confined space is treated by cation exchange with a Na-type weakly acidic cation-exchange resin; an organic-component decomposing device in which an organic component contained in water discharged from the cation-exchange device is decomposed, comprising a diamond-electrode electrolysis device including conductive diamond serving as an electrode, and a catalytic decomposition device; an electrodialysis device in which water discharged from the organic-component decomposing device is treated by electrodialysis, thereby producing an acid and an alkali; a regeneration unit in which the cation-exchange resin is regenerated using the acid and the alkali produced in the electrodialysis device; a mineral adding unit in which a mineral component is added to a treated water discharged from the electrodialysis device; a first tank that stores the acid and supplies the acid to the cation-exchange device to regenerate the cation-exchange resin; and a second tank that stores the alkali and supplies the alkali to the cation-exchange device to regenerate the cation-exchange resin.
5. The combination according to claim 4, wherein the wastewater is urine, which is treated by the cation-exchange device, and condensed water produced by condensing water vapor contained in air in the confined space is merged into the water from the cation-exchange device prior to the organic component is decomposed.
6. The water recovery system according to claim 1, wherein the alkali is supplied to the cation-exchange device after the acid is supplied and used for regeneration of the cation-exchange resin.
7. The combination according to claim 4, wherein the alkali is supplied to the cation-exchange device after the acid is supplied and used for regeneration of the cation-exchange resin.
Description
BRIEF DESCRIPTION OF DRAWINGS
(1)
(2)
(3)
DESCRIPTION OF EMBODIMENTS
(4) Hereafter, the present invention is described in detail with reference to the attached drawings.
(5)
(6) The wastewater treatment system includes a cation-exchange device 1 in which water to be treated, such as wastewater originating in a space station or the like, water discharged by the human body, water produced by condensing water vapor contained in the air, is directly treated by cation exchange; a diamond-electrode electrolysis device 2 in which organic substances, urea, and other nitrogen compounds contained in the water discharged from the cation-exchange device 1 are decomposed; a catalytic decomposition device 3 in which the residual organic component is brought into contact with a catalyst to be decomposed; an electrodialysis device 4 in which water discharged from the catalytic decomposition device 3 is treated by electrodialysis to produce desalted water as well as an acid and an alkali; and a mineral adding device 5 in which a mineral is added to the desalted water.
(7) In this embodiment, a Na-type weakly acidic cation-exchange resin is used as a cation-exchange resin included in the cation-exchange device 1. The Na-type weakly acidic cation-exchange resin has a larger cation-exchange capacity than strongly acidic cation-exchange resins. The Na-type weakly acidic cation-exchange resin has larger Ca.sup.2+ and Mg.sup.2+ exchange capacities than an H-type weakly acidic cation-exchange resin.
(8) In this embodiment, the hardness components are removed in the cation-exchange device 1, which prevents the ion-exchange membrane in the electrodialysis device 4 from being clogged. Organic substances such as protein, which may cause fouling of the ion-exchange membrane to occur, can be decomposed in the diamond-electrode electrolysis device 2 and the catalytic decomposition device 3.
(9) The acid produced in the electrodialysis device 4 is stored in a tank 6. The acid stored in the tank 6 is supplied to the cation-exchange device 1 when the cation-exchange resin included in the cation-exchange device 1 is regenerated and used for regenerating the cation-exchange resin. The waste fluid resulting from regeneration is introduced to a waste fluid tank 7. In this embodiment, the acid produced in the electrodialysis device 4 is used for regenerating the cation-exchange resin, which eliminates the need for an exclusive acid source.
(10) Although it is impossible to remove urea in the electrodialysis device 4, in this embodiment, urea is decomposed into ammonia and carbonic acid in the diamond-electrode electrolysis device 2 and the catalytic decomposition device 3. This prevents urea from leaking into the treated water.
(11) The details of the reaction mechanism in which impurities are removed in this embodiment are as follows.
(12) In the cation-exchange device 1, Ca.sup.2+, Mg.sup.2+, and some monovalent cations are removed by a cation-exchange reaction with a Na-type weakly acidic cation-exchange resin.
(13) The following softening reaction (i.e., hardness-component-removal reaction) occurs due to ion exchange.
CaX,MgX+RNa.fwdarw.RCa,RMg+NaX
(14) where,
(15) R: Exchange group of ion exchange resin
(16) In the diamond-electrode electrolysis and the catalyst decomposition, the organic substances and urea are decomposed by the following reactions.
Organic Substance.fwdarw.(Oxidation).fwdarw.Organic Acid and CO.sub.2
Urea.fwdarw.NH.sup.4++CO.sub.2.sup.2
2NH.sub.2+3HClO.fwdarw.N.sub.2+3H.sub.2O+3HCl
(17) Examples of the catalyst that can be included in the catalytic decomposition device 3 include, but are not limited to, Pt, Ru, Ni, and Co. It is suitable to operate the catalytic decomposition device 3 at the normal temperature to about 350 C.
(18) The following reaction occurs in the electrodialysis device.
YX+H.sub.2O.fwdarw.HX(acid)+YOH(alkali)
(19)
(20) Although the alkaline solution produced by electrodialysis is discharged into the waste fluid tank 7 in
(21) Gases such as hydrogen, oxygen, and chlorine are generated in the above-described diamond-electrode electrolysis device, catalytic decomposition device, electrodialysis device, and the like due to chemical reactions. It is preferable to perform gas-liquid separation as needed by, for example, using a degassing membrane or centrifugal separation.
(22) In the embodiments illustrated in
(23) The water recovery systems illustrated in
(24) In a confined space, the major sources of water to be treated are urine, water vapor contained in the air, and domestic wastewater. Since they have different water qualities, two or more kinds of the wastewater originating from a different source may be treated separately by the water recovery system of the present invention. Alternatively, two or more kinds of the wastewater may be mixed together and then treated. It is also possible to merge a specific type of water to be treated with water being treated during the treatment process. It is desirable to select from the above-described treatment methods in consideration with treatment efficiency.
(25) In general, urine contains the largest amount of scale component among the above-described wastewater to be treated. Therefore, only urine may be subjected to a hardness-component-removal treatment performed in the cation-exchange device 1, and condensed water produced by condensing water vapor contained in the air may merge into the water from the device 1 prior to the organic-component decomposition step. This increases treatment efficiency without increasing the amount of water to be treated in each step.
EXAMPLES
(26) Urine was experimentally treated in accordance with a treatment flow using the system of the present invention. As described above, urine is a representative example of the water to be treated which may originate in a confined space. Table 1 shows a major ion composition of the urine.
(27) TABLE-US-00001 TABLE 1 Concentration Ion species mg/L meq/L Cation NH.sub.3 572 34 Na.sup.+ 3146 137 Ca.sub.2.sup.+ 8 0.4 Mg.sub.2.sup.+ 199 16 K.sup.+ 1752 45 Total cation 232 Anion Cl.sup. 5645 159 NO.sub.3.sup. 586 9.5 SO.sub.4.sup.2 2076 43 PO.sub.4.sup.3 374 3.9 Total anion 212
[1] Cation-Exchange Treatment
(28) One liter of the urine described above was passed through 50 mL of a Na-type weakly acidic cation-exchange resin (C104E produced by Purolite Corporation). As a result, all the hardness components and part of NH.sub.3 and K.sup.+ were removed from the water treated by the Na-type cation resin. The concentrations of the residual NH.sub.3 and K.sup.+ were 520 mg/L and 1740 mg/L, respectively. The TOC of the water treated with the cation-exchange resin was 7600 mg/L.
(29) [2] Test of Decomposing Organic Substances by Diamond-Electrode Electrolysis Device
(30) Subsequently, 200 mL of the above-described water treated by the cation-exchange resin was treated by electrolysis using an electrolysis device including a 5-cm square diamond electrode at a circulation flow rate of 1.7 L/min. Electrolysis was performed at a constant current of 2.5 A for 100 hours. The voltage varied from 10 V to 5 V. A 20 mm500 mmH acrylic column filled with a catalyst was incorporated into the circulatory system. The catalyst was a TiPt catalyst produced by N.E. CHEMCAT Corporation. After 100 hours, the TOC of the electrolysis circulation water was 1 mg/L or less.
(31) [3] Desalting and Production of Acid and Alkali Using Electrodialysis Device
(32) An electrodialysis device prepared by modifying ACILYZER S3 produced by ASTOM Corporation was used in the test. The cell used was constituted by an anode, an electrode compartment, a bipolar membrane, an acid compartment, an anion-exchange membrane, a desalting compartment, a cation-exchange membrane, an alkaline compartment, a bipolar membrane, an electrode compartment, and a cathode. The electrode solution used was a 0.5 mol/L sodium sulfate solution.
(33) Electrolysis was performed at a constant current of 2.2 A. Circulation of the water treated with the diamond electrode was performed at a flow rate of 50 mL/min. The voltage varied from 10 V to 30 V.
(34) Through each of the acid compartment and the alkaline compartment, 50 mL of pure water was separately circulated at a flow rate of 10 mL/min. After 8 hours, the concentration in the water circulated through the acid compartment was about 1 N, at which the circulated water was capable of being used for regenerating the cation resin. Table 2 summarizes the quality of the desalted water which was determined after the 8-hour circulation period. In Table 2, the term Standard refers to a standard value of tap water.
(35) TABLE-US-00002 TABLE 2 Item Na.sup.+ NH.sub.4.sup.+ K.sup.+ Mg.sup.2+ Ca.sup.2+ Cl.sup. NO.sub.2.sup. NO.sub.3.sup. SO.sub.4.sup.2 PO.sub.4.sup.2 Measured 6.2 0.1 0.7 <0.1 0.1 0.2 2.1 3.8 11.3 7.9 value (mg/L) Standard 200 300*.sup.1 300*.sup.1 200 10*.sup.2 10*.sup.2 (mg/L) *.sup.1As calcium, magnesium, or the like *.sup.2As nitrate nitrogen or nitrite nitrogen
(36) As shown in Table 2, each ion concentration satisfied the tap water standard, and the water quality was suitable for drinking purpose.
INDUSTRIAL APPLICABILITY
(37) According to the present invention, reuse of water, which is vital to human life, may be achieved without concerns about clogging due to scale, fouling due to organic substances, and the like or consuming a large amount of energy as in evaporation. This enables humans to stay in a confined space such as a nuclear shelter or the space for a prolonged period of time.
(38) While details of the present invention are described with reference to specific embodiments, it is apparent to those skilled in the art that various modifications can be made without departing from the spirit and the scope of the present invention.
(39) This application is based on Japanese Patent Application (Japanese Patent Application No. 2013-009380) filed Jan. 22, 2013, which is hereby incorporated by reference herein in its entirety.