WO2020228638A1 - 一种电解盐溶液高效再生树脂的方法 - Google Patents
一种电解盐溶液高效再生树脂的方法 Download PDFInfo
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- WO2020228638A1 WO2020228638A1 PCT/CN2020/089409 CN2020089409W WO2020228638A1 WO 2020228638 A1 WO2020228638 A1 WO 2020228638A1 CN 2020089409 W CN2020089409 W CN 2020089409W WO 2020228638 A1 WO2020228638 A1 WO 2020228638A1
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- resin
- reaction
- titanium
- electrolytic salt
- salt solution
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- 239000011347 resin Substances 0.000 title claims abstract description 284
- 229920005989 resin Polymers 0.000 title claims abstract description 284
- 238000000034 method Methods 0.000 title claims abstract description 69
- 239000012266 salt solution Substances 0.000 title claims abstract description 41
- 230000001172 regenerating effect Effects 0.000 title claims abstract description 37
- 239000000243 solution Substances 0.000 claims abstract description 93
- 238000003795 desorption Methods 0.000 claims abstract description 90
- 238000011069 regeneration method Methods 0.000 claims abstract description 65
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims abstract description 53
- 239000003456 ion exchange resin Substances 0.000 claims abstract description 52
- 229920003303 ion-exchange polymer Polymers 0.000 claims abstract description 52
- 238000003487 electrochemical reaction Methods 0.000 claims abstract description 47
- 230000008929 regeneration Effects 0.000 claims abstract description 45
- 239000007788 liquid Substances 0.000 claims abstract description 41
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims abstract description 40
- 238000006243 chemical reaction Methods 0.000 claims abstract description 32
- 239000011780 sodium chloride Substances 0.000 claims abstract description 20
- 239000002699 waste material Substances 0.000 claims abstract description 15
- 238000011001 backwashing Methods 0.000 claims abstract description 5
- 238000005868 electrolysis reaction Methods 0.000 claims description 30
- 239000003792 electrolyte Substances 0.000 claims description 27
- 238000006276 transfer reaction Methods 0.000 claims description 25
- 229910000428 cobalt oxide Inorganic materials 0.000 claims description 20
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 15
- 239000010949 copper Substances 0.000 claims description 15
- 229910000431 copper oxide Inorganic materials 0.000 claims description 15
- 239000007921 spray Substances 0.000 claims description 15
- 125000004122 cyclic group Chemical group 0.000 claims description 13
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 claims description 11
- QLGFXFCQAIDVFZ-UHFFFAOYSA-N [Ti].[Ti].[Ir].[Ru] Chemical compound [Ti].[Ti].[Ir].[Ru] QLGFXFCQAIDVFZ-UHFFFAOYSA-N 0.000 claims description 9
- 229910045601 alloy Inorganic materials 0.000 claims description 7
- 239000000956 alloy Substances 0.000 claims description 7
- HJPBEXZMTWFZHY-UHFFFAOYSA-N [Ti].[Ru].[Ir] Chemical compound [Ti].[Ru].[Ir] HJPBEXZMTWFZHY-UHFFFAOYSA-N 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 229910052719 titanium Inorganic materials 0.000 claims description 6
- -1 ruthenium iridium titanium-copper-nickel Chemical compound 0.000 claims description 5
- 229910000570 Cupronickel Inorganic materials 0.000 claims description 4
- 239000003957 anion exchange resin Substances 0.000 claims description 4
- MVMKJZBBDIKJKP-UHFFFAOYSA-N [Co].[Ru].[Ir].[Ti] Chemical compound [Co].[Ru].[Ir].[Ti] MVMKJZBBDIKJKP-UHFFFAOYSA-N 0.000 claims description 3
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
- AYFPISJIGHKBBU-UHFFFAOYSA-N [Ir].[Ru].[Cu].[Ti] Chemical group [Ir].[Ru].[Cu].[Ti] AYFPISJIGHKBBU-UHFFFAOYSA-N 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- BASYJLWAYAUJBW-UHFFFAOYSA-N [Ti].[Ir].[Ru].[Pt] Chemical compound [Ti].[Ir].[Ru].[Pt] BASYJLWAYAUJBW-UHFFFAOYSA-N 0.000 claims 1
- 229920001429 chelating resin Polymers 0.000 claims 1
- 238000001179 sorption measurement Methods 0.000 abstract description 58
- MMDJDBSEMBIJBB-UHFFFAOYSA-N [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] MMDJDBSEMBIJBB-UHFFFAOYSA-N 0.000 abstract description 45
- 229920006395 saturated elastomer Polymers 0.000 abstract description 12
- 239000008151 electrolyte solution Substances 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 description 17
- 229910052801 chlorine Inorganic materials 0.000 description 17
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 16
- 239000002351 wastewater Substances 0.000 description 16
- 230000008569 process Effects 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 229910002651 NO3 Inorganic materials 0.000 description 11
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 11
- 230000008859 change Effects 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 239000012492 regenerant Substances 0.000 description 9
- 239000003344 environmental pollutant Substances 0.000 description 7
- 238000001728 nano-filtration Methods 0.000 description 7
- 231100000719 pollutant Toxicity 0.000 description 7
- 238000005516 engineering process Methods 0.000 description 6
- 239000012528 membrane Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 238000000108 ultra-filtration Methods 0.000 description 4
- 238000005345 coagulation Methods 0.000 description 3
- 230000015271 coagulation Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000003673 groundwater Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- FMPKBTUFVFWPQW-UHFFFAOYSA-N [Ru].[Ir].[Pt] Chemical compound [Ru].[Ir].[Pt] FMPKBTUFVFWPQW-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 230000002925 chemical effect Effects 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- YOCUPQPZWBBYIX-UHFFFAOYSA-N copper nickel Chemical group [Ni].[Cu] YOCUPQPZWBBYIX-UHFFFAOYSA-N 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- 229910001448 ferrous ion Inorganic materials 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000010842 industrial wastewater Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000012465 retentate Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 238000002336 sorption--desorption measurement Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000002352 surface water Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Images
Classifications
-
- 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
- B01J49/00—Regeneration or reactivation of ion-exchangers; Apparatus therefor
Definitions
- the invention belongs to the field of resin regeneration, and specifically relates to a method for efficiently regenerating resin from an electrolytic salt solution.
- Resin adsorption is an important technology in the field of water treatment. Its principle is that the resin absorbs pollutants in water through physical and chemical effects and removes them from the water. Resin can remove nitrates, organics, heavy metals, etc. in water. The use of anion exchange method to remove nitrate nitrogen in groundwater has been listed as one of the US Environmental Protection Agency (Environmental Protection Agency, EPA) recommended technologies. Resin adsorption to remove pollutants in water has the characteristics of high removal efficiency and stable water outlet operation. However, resin regeneration is a bottleneck restricting the large-scale application of resin adsorption technology. It mainly includes two problems: 1.
- Patent CN101870505A discloses a method for advanced treatment and reuse of powder resin for printing and dyeing wastewater.
- the printing and dyeing wastewater treated by biotechnology is filtered, and the powder resin is fully mixed and contacted in the reactor to precipitate and separate.
- the separated powder resin is transported to the desorption tank for desorption with a desorption solution containing an inorganic desorption agent, washed with water, and transported to the reactor for reuse.
- the method has simple process, low investment and good treatment effect, and can be realized by simple modification on the existing biochemical treatment system, but the method will produce a large amount of high-salt desorption liquid which is difficult to handle.
- Patent CN102050554A discloses a method for the treatment of high-concentration resin desorption liquid based on deep purification of wastewater, which mainly intercepts the high-concentration resin desorption liquid through nanofiltration membranes, and the nanofiltration permeate is oxidized and reused as a desorption agent , Add coagulant to the nanofiltration retentate for coagulation and precipitation, perform Fenton oxidation or ozone oxidation on the supernatant after coagulation and precipitation, and return the coagulation and precipitation liquid to the biochemical system of the biochemical tail water section for further processing Biodegradation, this method realizes the recycling treatment of high-concentration desorption liquid, but still has the problems of using a large amount of chemical agents, high cost, and serious membrane pollution.
- Patent CN103408102A discloses an ion exchange resin regeneration method that reduces the amount of desorption liquid.
- the resin is regenerated with the regeneration liquid and becomes the desorption liquid.
- the desorption liquid is coagulated to form a clear liquid.
- the regenerated liquid is prepared for recycling and regeneration. There are multiple batches of resin.
- This method has high regeneration agent utilization rate and low desorption liquid output, which saves desorption liquid disposal costs.
- no good desorption liquid disposal method has been proposed, and the recycling of recycled resin may cause The damage of the resin reduces the service life.
- Patent CN103193364A discloses a resource utilization method of ion exchange resin desorption liquid.
- the resin desorption liquid is separated into a concentrated liquid with high organic concentration and a filtrate with low turbidity through an ultrafiltration membrane system.
- the concentrated liquid is acidic Ferrous ions and hydrogen peroxide are added in the environment to generate activated sludge nutrient solution rich in ferric iron and high biodegradability;
- the ultrafiltration filtrate enters the nanofiltration membrane system for separation, resulting in a clear filtrate and a small amount of Concentrate;
- the nanofiltration concentrate is refluxed into the ultrafiltration system, and sodium chloride is added to the nanofiltration filtrate to be used as a resin regenerating agent.
- This method separates the high-concentration organics and salts in the resin desorption solution for comprehensive utilization.
- the resource utilization of the ion exchange resin desorption liquid is realized, but the process of the method is complicated, and both the ultrafiltration membrane and the nanofiltration membrane are easily contaminated, which increases the difficulty and cost of processing.
- Patent CN105080624A discloses an ion exchange resin regeneration method.
- the resin column is backwashed with dilute regeneration solution and then positive washed with dilute sulfuric acid to achieve the purpose of efficiently regenerating resin.
- the degree of ion regeneration resin recovery is as high as 80-90%.
- the utilization rate of the regenerated liquid is improved, the regeneration cost is obviously reduced, and the resin performance is restored well.
- this method only regenerates D001 (732) macroporous strong acid cation exchange resin and has a narrow application range.
- the dilute regenerant used is a mixture of sulfuric acid and copper sulfate, which may introduce the risk of other pollutants, and this method is not mentioned. Disposal of regenerated liquid.
- the purpose of the present invention is to provide a method for efficiently regenerating resin from an electrolytic salt solution on the basis of the prior art.
- a method for efficiently regenerating resin from electrolytic salt solution which includes the following steps:
- the present invention is based on the characteristics that the resin needs to desorb and treat the desorption solution after adsorbing pollutants, adopts electrochemical technology to regenerate the resin, optimizes the reaction conditions, and provides a method for efficiently regenerating resin from an electrolytic salt solution to efficiently remove nitric acid in wastewater Salt nitrogen and some organic matter, while environmentally friendly and convenient treatment of resin desorption liquid.
- the resin desorption solution obtained after backwashing the filled ion exchange resin can be passed into the spray tower before the electrochemical reaction, and mass transfer with the chlorine generated during the electrolysis reaction
- the specific steps of the reaction are as follows: the resin desorption solution obtained in step (2) is first introduced into the spray tower, and the mass transfer reaction is carried out with the chlorine gas generated during the electrolysis reaction in step (1), and the resin after the mass transfer reaction is desorbed
- the liquid undergoes an electrochemical reaction to obtain a liquid effluent.
- the effluent is passed from the bottom of the resin column to backwash the filled ion exchange resin, and the waste liquid after the backwash undergoes an electrochemical reaction, thus performing a cyclic reaction.
- the present invention regenerates the resin through electrochemical technology. After the resin adsorbs pollutants, it also needs to desorb and treat the desorption liquid. Under other conditions, the NaCl solution is electrolyzed to remove the electrolyte from the ion exchange resin. Pass through the bottom of the resin column to backwash the filled ion exchange resin to obtain a resin desorption solution, and then subject the resin desorption solution to electrochemical reaction treatment. The resin desorption solution that is passed into the electrochemical reactor undergoes an electro-reduction oxidation process , Has the advantage of efficiently removing nitrate nitrogen and part of organic matter in wastewater.
- the resin desorption solution obtained after backwashing the filled ion exchange resin is performed before the electrochemical reaction , It can be passed into the spray tower first to carry out the mass transfer reaction with the chlorine produced during the electrolysis reaction.
- the chlorine dissolves in water and becomes free chlorine, it can supplement the chlorine ions in the circulating solution and avoid the addition of chlorine during the circulation process.
- Sodium sulfide is beneficial to the desorption of the resin, effectively reducing the treatment cost, and solving the significant defect that the resin desorption liquid is difficult to handle in the resin adsorption water treatment technology.
- the electrochemical reactor when an electrochemical reaction is carried out in an electrochemical reactor, the electrochemical reactor includes an anode and a cathode, wherein the anode-cathode is ruthenium iridium titanium-copper, ruthenium iridium titanium- Cobalt, ruthenium-iridium-titanium-based cobalt oxide, ruthenium-iridium-titanium-copper-nickel alloy, ruthenium-iridium-titanium-based copper/cobalt oxide, ruthenium-iridium-platinum, graphite-iron, boron-doped diamond-copper-nickel alloy or Boron-doped diamond-titanium-based copper/cobalt oxide.
- the anode-cathode is ruthenium iridium titanium-copper, ruthenium iridium titanium- Cobalt, ruthenium-iridium-titanium-based cobalt oxide, rut
- composition of the copper-nickel alloy submitted above may be, for example, ruthenium-iridium-titanium-copper-nickel alloy (65Ni-32Cu-1Fe) and boron-doped diamond-copper-nickel alloy (65Ni-32Cu-1Fe).
- the anode-cathode is ruthenium-iridium-titanium-based copper/cobalt oxide, ruthenium-iridium-titanium-based cobalt oxide or boron-doped diamond-titanium-based copper/cobalt oxide.
- the area ratio of the cathode to the anode is 1:0.1 to 1:2.5; more preferably, it is 1:0.5 to 1:2.
- the ion exchange resin used in the present invention is a macroporous strongly basic anion exchange resin, preferably a quaternary ammonium salt resin with a styrene skeleton.
- the ion exchange resin used in the present invention is A850, A520E, D201, 201 D202, mp62-A or IRA-900.
- the macroporous strong basic anion exchange resin used in the present invention is not limited to the above-mentioned several resins, and any specific anion exchange resin can be used without affecting the effect of the present invention.
- the current density during the electrochemical reaction is 3 to 150 mA/cm 2 ; preferably 5 to 100 mA/cm 2 .
- the electrochemical reaction time is 0.3 to 3 hours, preferably 0.5 to 2 hours.
- the amount of NaCl solution used during electrolysis is 1 to 5 BV; preferably 1.5 to 3 BV.
- the mass concentration of the NaCl solution is 1%-20%; preferably 5%-10%.
- the voltage is 1-30V; preferably 5-20V.
- the electrolysis reaction time is 5 to 15 minutes.
- the flow rate of the electrolyte from the bottom of the resin column is 0.1-10 BV/h; preferably 0.2-5 BV/h.
- the flow rate of the effluent from the bottom of the resin column is 0.1-10 BV/h; preferably 0.2-5 BV/h.
- the reaction is stopped after the entire regeneration reaction has progressed for 1 to 5 hours, the resin column is replaced, and step (2) is continued.
- the method for regenerating resin is flexible and requires only regular replacement of the resin column, the device is simple and easy to operate, and has high economic feasibility.
- the recovery degree of the resin can generally reach about 75%.
- the recovery degree of the resin of the present invention is higher than that of the existing method.
- the nitrate can be almost completely removed, which is an efficient regeneration. Resin and remove nitrate nitrogen and some organic matter in wastewater.
- the present invention adopts an electrochemical method to treat the resin desorption solution, and the removal efficiency of nitrate nitrogen is high, which can reach 85% to 100%, and the nitrogen selectivity is good;
- the method for efficiently regenerating resin from the electrolytic salt solution provided by the present invention avoids secondary pollution caused by the difficulty of processing a high-concentration resin desorption solution, and the effluent after electrochemical reaction treatment contains free chlorine, which is beneficial to the resin Regeneration, the re-adsorption capacity of the resin after regeneration can reach 80%-95% of the saturated resin adsorption capacity before regeneration, and the resin sphere rate after regeneration is only reduced by 5%-17% compared to the resin sphere rate before regeneration , The structure of the resin has not changed significantly, while saving the amount of NaCl and reclaimed water;
- the method for efficiently regenerating resin from the electrolytic salt solution provided by the present invention is flexible and requires only regular replacement of the resin column, the device is simple and easy to operate, and has high economic feasibility.
- Figure 1 is a schematic diagram of the present invention
- a chemical plant wastewater is filled with 10g
- the resin column of A520E resin adsorbs nitrate. After the adsorption equilibrium is reached, the concentration of nitrate nitrogen in the adsorption and desorption solution of the resin column is 119mg/L.
- the method of efficiently regenerating resin from electrolytic salt solution is carried out according to the following steps:
- the 1BV mass concentration of 5% NaCl solution is electrolyzed in an electrochemical reactor at a constant voltage of 5V DC voltage for 10 minutes to obtain an electrolyte.
- the anode-cathode in the electrochemical reactor is ruthenium-iridium-titanium-titanium-based cobalt oxidation Object electrode pair, the area ratio of cathode to anode is 1:1;
- the content of nitrate nitrogen in the adsorption and desorption solution is 119mg/L
- the nitrate nitrogen concentration in the effluent is 11mg/L, and the nitrate nitrogen removal rate can reach 90 ⁇ 3%.
- the regenerated resin is desorbed again.
- the re-adsorption capacity of the resin can reach 86 ⁇ 2% of the saturated resin adsorption capacity before regeneration.
- the sphere rate of the regenerated resin is 77 ⁇ 3%, compared with The initial resin sphericity was only reduced by 11%, and the resin structure did not change significantly.
- Huai chemical plant wastewater is filled with 35g
- the resin column of A520E resin adsorbs nitrate. After the adsorption equilibrium is reached, the nitrate nitrogen concentration in the adsorption and desorption solution of the resin column is 1022mg/L, and the TOC is 26mg/L.
- the 5BV mass concentration of 15% NaCl solution was electrolyzed in an electrochemical reactor at a constant voltage of 20V DC voltage for 10 minutes to obtain an electrolyte.
- the anode-cathode in the electrochemical reactor was ruthenium-iridium-titanium-titanium-based copper/ Cobalt oxide electrode pair, the area ratio of cathode to anode is 1:0.8;
- the nitrate nitrogen content in the adsorption and desorption solution is 1022mg/L, and the TOC is 26mg/L A520E resin, after being treated by the above-mentioned electrolytic salt solution high-efficiency resin regeneration method, the TOC in the effluent is 1mg/L, the nitrate nitrogen concentration is 18mg/L, the TOC removal rate can reach 96 ⁇ 3%, and the nitrate nitrogen removal rate It can reach 98 ⁇ 3%.
- Re-adsorption of the regenerated resin after 8 adsorption-regeneration cycles can reach 75 ⁇ 3% of the saturated resin adsorption capacity before regeneration, and the sphere rate of the regenerated resin is 71 ⁇ 2%.
- the initial resin sphericity was only reduced by 17%, and the resin structure did not change significantly.
- a factory wastewater is filled with 5g
- the resin column of D201 resin adsorbs nitrate. After the adsorption equilibrium is reached, the nitrate nitrogen concentration in the adsorption and desorption solution of the resin column is 44mg/L.
- the method of electrolytic salt solution to efficiently regenerate resin is carried out according to the following steps:
- the anode-cathode in the electrochemical reactor is a pair of ruthenium-iridium-titanium-cobalt electrodes.
- the area ratio of cathode to anode is 1:1.2;
- the content of nitrate nitrogen in the adsorption and desorption solution is 44mg/L
- the nitrate nitrogen concentration in the effluent is 5mg/L
- the nitrate nitrogen removal rate can reach 88 ⁇ 2%.
- Re-adsorption of the regenerated resin after 6 adsorption-regeneration cycles can reach 87 ⁇ 3% of the saturated resin adsorption capacity before regeneration, and the sphere rate of the regenerated resin is 83 ⁇ 2%, which is higher than
- the initial resin sphericity was only reduced by 5%, and the resin structure did not change significantly.
- a factory wastewater is filled with 5g
- the resin column of D201 resin adsorbs nitrate. After the adsorption equilibrium is reached, the concentration of nitrate nitrogen in the adsorption and desorption solution of the resin column is 57mg/L.
- the method of efficiently regenerating resin from electrolytic salt solution is carried out according to the following steps:
- the anode-cathode in the electrochemical reactor is boron-doped diamond-titanium-based copper/ Cobalt oxide electrode pair, the area ratio of cathode to anode is 1:1.5;
- the nitrate nitrogen content in the adsorption and desorption solution is 57mg/L
- the nitrate nitrogen concentration in the effluent is 6mg/L, and the nitrate nitrogen removal rate can reach 89 ⁇ 2%.
- the regenerated resin is desorbed again.
- the re-adsorption capacity of the resin can reach 90 ⁇ 2% of the saturated resin adsorption capacity before regeneration.
- the sphere rate of the regenerated resin is 81 ⁇ 3%.
- the initial resin sphericity was only reduced by 7%, and the resin structure did not change significantly.
- Waste water from a factory in Yancheng is filled with 20g
- the resin column of the IRA-900 resin adsorbs nitrate. After the adsorption equilibrium is reached, the nitrate nitrogen concentration in the adsorption and desorption solution of the resin column is 813mg/L.
- the method of efficiently regenerating resin from the electrolytic salt solution is carried out according to the following steps:
- an electrolyte is obtained.
- the anode-cathode in the electrochemical reactor is boron-doped diamond-titanium-based copper/ Cobalt oxide electrode pair, the area ratio of cathode to anode is 1:0.5;
- the nitrate nitrogen content in the adsorption desorption solution is 813mg/L
- the nitrate nitrogen concentration in the effluent is 13mg/L
- the nitrate nitrogen removal rate can reach 98 ⁇ 3%.
- the regenerated resin is desorbed again.
- the re-adsorption capacity of the resin can reach 84 ⁇ 1% of the saturated resin adsorption capacity before regeneration, and the sphere rate of the regenerated resin is 74 ⁇ 3%, which is higher than
- the initial resin sphericity was only reduced by 14%, and the resin structure did not change significantly.
- a factory in Nanjing was filled with 15g of wastewater
- the resin column of IRA-900 resin adsorbs nitrate. After the adsorption equilibrium is reached, the concentration of nitrate nitrogen in the adsorption and desorption solution of the resin column is 482 mg/L.
- the method of efficiently regenerating resin from electrolytic salt solution is carried out according to the following steps:
- the 4BV mass concentration of 8% NaCl solution was electrolyzed in an electrochemical reactor at a constant voltage of 15V DC voltage for 10 minutes to obtain an electrolyte.
- the anode-cathode in the electrochemical reactor was ruthenium-iridium-titanium-titanium-based copper/ Cobalt oxide electrode pair, the area ratio of cathode to anode is 1:2;
- the nitrate nitrogen content in the adsorption and desorption solution is 482mg/L
- the nitrate nitrogen concentration in the effluent is 15mg/L, and the nitrate nitrogen removal rate can reach 96 ⁇ 1%.
- the regenerated resin is desorbed again.
- the re-adsorption capacity of the resin can reach 82 ⁇ 2% of the saturated resin adsorption capacity before regeneration.
- the sphere rate of the regenerated resin is 78 ⁇ 3%, which is higher than The initial resin sphericity was only reduced by 10%, and the resin structure did not change significantly.
- a factory wastewater is filled with 10g
- the resin column of A520E resin adsorbs nitrate. After the adsorption equilibrium is reached, the concentration of nitrate nitrogen in the adsorption and desorption solution of the resin column is 225 mg/L.
- the method of efficiently regenerating resin from electrolytic salt solution is carried out according to the following steps:
- an electrolyte is obtained.
- the anode-cathode in the electrochemical reactor is ruthenium-iridium-titanium-titanium-based copper /Cobalt oxide electrode pair, the area ratio of cathode to anode is 1:1.8;
- the content of nitrate nitrogen in the adsorption and desorption solution is 225mg/L
- the nitrate nitrogen concentration in the effluent is 14mg/L
- the nitrate nitrogen removal rate can reach 94 ⁇ 3%.
- Re-adsorption of the regenerated resin after 6 adsorption-regeneration cycles can reach 85 ⁇ 2% of the saturated resin adsorption capacity before regeneration, and the sphere rate of the regenerated resin is 80 ⁇ 2%, which is higher than
- the initial resin sphericity was only reduced by 6%, and the resin structure did not change significantly.
- the 1.5BV mass concentration of 8% NaCl solution is electrolyzed in an electrochemical reactor at a constant voltage of 10V DC voltage for 15 minutes to obtain an electrolyte.
- the anode-cathode in the electrochemical reactor is ruthenium-iridium-titanium-titanium-based cobalt Oxide electrode pair, the area ratio of cathode to anode is 1:1.8;
- the nitrate nitrogen content in the adsorption and desorption solution is 177mg/L
- the nitrate nitrogen concentration in the effluent is 10mg/L
- the nitrate nitrogen removal rate can reach 94 ⁇ 3%.
- the regenerated resin is desorbed again.
- the re-adsorption capacity of the resin can reach 83 ⁇ 4% of the saturated resin adsorption capacity before regeneration.
- the sphere rate of the regenerated resin is 78 ⁇ 2%, which is higher than The initial resin sphericity was only reduced by 9%, and the resin structure did not change significantly.
- a factory wastewater is filled with 20g
- the resin column of D202 resin adsorbs nitrate. After the adsorption equilibrium is reached, the concentration of nitrate nitrogen in the adsorption and desorption solution of the resin column is 598 mg/L.
- the method of efficiently regenerating resin from electrolytic salt solution is carried out according to the following steps:
- the 4BV mass concentration of 12% NaCl solution is electrolyzed in an electrochemical reactor at a constant voltage of 10V DC voltage for 10 minutes to obtain an electrolyte.
- the anode-cathode in the electrochemical reactor is ruthenium-iridium-titanium-titanium-based copper/ Cobalt oxide electrode pair, the area ratio of cathode to anode is 1:1;
- the content of nitrate nitrogen in the adsorption and desorption solution is 598mg/L
- the nitrate nitrogen concentration in the effluent is 9mg/L
- the nitrate nitrogen removal rate can reach 99 ⁇ 3%.
- Re-adsorption of the regenerated resin after 6 adsorption-regeneration cycles can reach 82 ⁇ 3% of the saturated resin adsorption capacity before regeneration, and the sphere rate of the regenerated resin is 73 ⁇ 3%, which is higher than
- the initial resin sphericity was only reduced by 13%, and the resin structure did not change significantly.
- the 1BV mass concentration of 10% NaCl solution is electrolyzed in an electrochemical reactor at a constant voltage of 10V DC voltage for 15 minutes to obtain an electrolyte.
- the anode-cathode in the electrochemical reactor is ruthenium-iridium-titanium-titanium-based copper/ Cobalt oxide electrode pair, the area ratio of cathode to anode is 1:1;
- the content of nitrate nitrogen in the adsorption and desorption solution is 641mg/L, and the TOC is 22mg/L
- the nitrate nitrogen concentration in the effluent is 9mg/L
- the TOC is 0.4mg/L
- the nitrate nitrogen removal rate can reach 99 ⁇ 3%.
- the removal rate of organic matter can reach 98 ⁇ 3%.
- Re-adsorption of the regenerated resin after 5 adsorption-regeneration cycles can reach 80 ⁇ 3% of the saturated resin adsorption capacity before regeneration.
- the sphere rate of the regenerated resin is 72 ⁇ 2%.
- the initial resin sphericity was only reduced by 16%, and the resin structure did not change significantly.
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Abstract
本发明涉及一种电解盐溶液高效再生树脂的方法,属于树脂再生领域。本发明提供的电解盐溶液高效再生树脂的方法,包括以下步骤:(1)将质量浓度为1~20%NaCl 溶液以1~30V电压进行电解反应后,得到电解液;(2)将上述电解液从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;(3)将上述树脂脱附液进行电化学反应后,得到流出液,所述流出液从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液进行电化学反应,如此进行循环反应。本发明的再生树脂的方法,去除硝酸盐氮效率高,达到85%~100%,再生后的树脂再吸附的吸附量为再生前树脂饱和吸附量的80%~95%。
Description
本发明属于树脂再生领域,具体涉及一种电解盐溶液高效再生树脂的方法。
近年来,随着我国经济和社会的高速发展,工业废水,农业用水和生活污水等的大量排放,自然界水体中各类污染物浓度急剧升高,地表水和地下水均遭受严重污染,受污染的水体会对动植物的生长造成严重的影响,这些污染物在饮用水中的存在也会危害人体健康。
树脂吸附是水处理领域的一个重要技术,其原理是树脂通过物理作用和化学作用吸附水中污染物质,将其从水中去除。树脂能够去除水中的硝酸盐、有机物、重金属等。使用阴离子交换法去除地下水中硝酸盐氮已列为美国环境保护署(Environmental Protection Agency,EPA)推荐技术之一。树脂吸附去除水中污染物具有去除效率高,出水运行稳定的特点,但树脂再生是制约树脂吸附技术大规模应用的一个瓶颈,主要包括两个方面的问题:1、树脂再生不彻底,导致树脂吸附能力降低,树脂寿命减少,增加成本;2、树脂再生时需要使用大量化学药剂,工业上大多采用酸、碱、食盐溶液进行再生,产生大量高盐脱附液,难以处理和回收利用。
专利CN101870505A公开了一种粉体树脂用于印染废水深度处理及回用的方法,将生物技术处理后的印染废水经过滤,在反应器中与粉体树脂充分混合接触反应后沉淀分离,将沉淀分离出的粉体树脂输送至脱附槽中用含无机脱附剂的脱附液脱附,水洗后输送至反应器中再次使用。该方法工艺简单、投资较少、处理效果好,且可在现有生化处理系统上通过简单改造实现该工艺,但该方法会产生大量高盐脱附液难以处理。专利CN102050554A公开了一种基于深度净化废水后树脂高浓脱附液的处置方法,主要是将树脂高浓脱附液经纳滤膜截留,纳滤透过液经氧化后作为脱附剂重复利用,在纳滤截留液中加入混凝剂进行混凝沉淀,对混凝沉淀后的上清液进行Fenton氧化或臭氧氧化,将混凝沉淀后的液体返回到生化尾水段的生化系统进一步进行生物降解,该方法实现了高浓脱附液的循环处理,但仍然存在使用大量化学药剂、成本高、膜污染严重等问题。专利CN103408102A公开了一种使脱附液减量化的离子交换树脂再生方法,用再生液再生树脂后成为脱附液,将此脱附液进行混凝形成清液,配制再生液进行循环套用再生树脂多个批次,该方法再生剂利用率高,脱附液产量低,节约了脱附液处置费用,但并未提出良好的脱附液处置方法,且再生液循环套用再生树脂有可能造成树脂的损坏,减少使用寿命。
专利CN103193364A公开了一种离子交换树脂脱附液的资源化利用的方法,将树脂脱附 液通过超滤膜系统分离成有机物浓度高的浓缩液和浊度低的滤出液,浓缩液在酸性环境下加入亚铁离子和过氧化氢氧化,生成富含三价铁可生化性高的活性污泥营养液;超滤滤出液进入纳滤膜系统分离,产生澄清的滤出液和少量的浓缩液;纳滤浓缩液回流进入超滤系统,纳滤滤出液添加氯化钠配制成树脂再生剂使用,该方法将树脂脱附液中高浓度的有机物和盐进行分离,分别进行综合利用,实现了离子交换树脂脱附液的资源化利用,但该方法工艺复杂,超滤膜和纳滤膜都容易被污染,增加了处理难度和成本。
专利CN105080624A公开了一种离子交换树脂再生方法,通过对树脂柱用稀再生液先进行反洗,再用稀硫酸进行正洗,达到高效再生树脂的目的,离子再生树脂恢复程度高达80~90%,再生液的利用率提高,再生费用明显降低,树脂性能恢复良好。但该方法只针对D001(732)大孔强酸阳离子交换树脂进行再生,应用范围较窄,所用稀再生液为硫酸和硫酸铜混合液,可能存在引入其他污染物的风险,且该方法未提及再生液的处置问题。
发明内容
本发明的目的是在现有技术的基础上,提供一种电解盐溶液高效再生树脂的方法。
本发明的技术方案如下:
一种电解盐溶液高效再生树脂的方法,它包括以下步骤:
(1)将质量浓度为1~20%NaCl溶液以1~30V电压进行电解反应后,得到电解液;
(2)将上述电解液从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)将上述树脂脱附液进行电化学反应后,得到流出液,所述流出液从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液进行电化学反应,如此进行循环反应。
本发明基于树脂吸附污染物后还需要脱附并处理脱附液的特点,采用电化学技术再生树脂,优选反应条件,提供一种电解盐溶液高效再生树脂的方法,以高效去除废水中的硝酸盐氮和部分有机物,同时对树脂脱附液进行环保、便捷的处理。
在一种优选方案中,对填充的离子交换树脂进行反洗后得到的树脂脱附液,在进行电化学反应之前,可以先通入喷淋塔中,与电解反应时产生的氯气进行传质反应,具体步骤如下:将步骤(2)得到的树脂脱附液先通入喷淋塔中,与步骤(1)中电解反应时产生的氯气进行传质反应,传质反应后的树脂脱附液再进行电化学反应,得到液出液,所述流出液从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液进行电化学反应,如此进行循环反应。
本发明通过电化学技术再生树脂,利用树脂吸附污染物后还需要脱附并处理脱附液的特点,在其他条件配合的情况下,将NaCl溶液电解后将电解液从填充有离子交换树脂的树脂柱 底部通入,对填充的离子交换树脂进行反洗,得到树脂脱附液,再将树脂脱附液进行电化学反应处理,通入电化学反应器的树脂脱附液经电还原氧化过程,具有高效去除废水中的硝酸盐氮和部分有机物的优势,同时在本发明的再生树脂处理方法中,对填充的离子交换树脂进行反洗后得到的树脂脱附液,在进行电化学反应之前,可以先通入喷淋塔中,与电解反应时产生的氯气进行传质反应,由于氯气溶于水成为游离氯,可以补充循环溶液中的氯离子,可避免在循环过程中补充投加氯化钠,从而有利于树脂的脱附,有效降低了处理成本,解决了树脂吸附水处理技术中树脂脱附液难以处理这一显著缺陷。
本发明提供的电解盐溶液高效再生树脂的方法,在电化学反应器中进行电化学反应时,电化学反应器包括阳极和阴极,其中,阳极-阴极为钌铱钛-铜、钌铱钛-钴、钌铱钛-钛基钴氧化物、钌铱钛-铜镍合金、钌铱钛-钛基铜/钴氧化物、钌铱钛-铂、石墨-铁、掺硼金刚石-铜镍合金或掺硼金刚石-钛基铜/钴氧化物。上述提交的铜镍合金的组成,例如可以为:钌铱钛-铜镍合金(65Ni-32Cu-1Fe)、掺硼金刚石-铜镍合金(65Ni-32Cu-1Fe)。
在一种优选方案中,阳极-阴极为钌铱钛-钛基铜/钴氧化物、钌铱钛-钛基钴氧化物或掺硼金刚石-钛基铜/钴氧化物。
在一种更优选方案中,阴极与阳极的面积比为1:0.1~1:2.5;进一步优选为1:0.5~1:2。例如,1:0.1、1:0.5、1:0.8、1:1.0、1:1.2、1:1.5、1:1.8、1:2.0或1:2.5。
在一种优选方案中,本发明采用的离子交换树脂为大孔强碱性阴离子交换树脂,优选为具有苯乙烯骨架的季铵盐树脂。
例如,本发明采用的离子交换树脂为
A850、
A520E、
D201、
201、
D202、
mp62-A或
IRA-900。但本发明采用的大孔强碱性阴离子交换树脂并不局限于上述提到的几种树脂,在任何不影响本发明效果的情况下,可以采用任何一种具体的阴离子交换树脂。
本发明的再生树脂的方法,进行电化学反应时的电流密度为3~150mA/cm
2;优选为5~100mA/cm
2。
进一步的,进行电化学反应时间为0.3~3h,优选为0.5~2h。
本发明的再生树脂的方法,进行电解反应时,NaCl溶液的用量为1~5BV;优选为1.5~3BV。
进一步的,进行电解反应时,NaCl溶液的质量浓度为1%~20%;优选为5%~10%。
进一步的,进行电解反应时,电压为1~30V;优选为5~20V。
进一步的,电解反应的时间为5~15min。
在一种方案中,电解液从树脂柱底部通入的流速为0.1~10BV/h;优选为0.2~5BV/h。
进一步的,流出液从树脂柱底部通入的流速为0.1~10BV/h;优选为0.2~5BV/h。
本发明的再生树脂的方法,在整个再生反应进行1~5h后停止反应,更换树脂柱,继续步骤(2)。该再生树脂的方法灵活机动,只需定期更换树脂柱,装置简单易操作,具有较高的经济可行性。
现有树脂再生方法中,批次吸附—再生后,树脂的恢复程度一般可以达到75%左右,本发明树脂的恢复程度比现有方法高,同时可以几乎完全去除硝酸盐,是一种高效再生树脂并且去除废水中的硝酸盐氮和部分有机物的方法。
采用本发明的技术方案,优势如下:
(1)本发明采用电化学方法处理树脂脱附液,去除硝酸盐氮效率高,可以达到85%~100%,氮气选择性好;
(2)本发明提供的电解盐溶液高效再生树脂的方法,避免了高浓度树脂脱附液难以处理带来的二次污染,且电化学反应处理后的流出液中含有游离氯,有利于树脂再生,再生后的树脂再吸附的吸附量能达到再生前树脂饱和吸附量的80%~95%,再生后的树脂圆球率相对于再生前的树脂圆球率只降低了5%~17%,树脂的结构未发生明显变化,同时节约了NaCl和再生用水的用量;
(3)本发明提供的电解盐溶液高效再生树脂的方法,灵活机动,只需定期更换树脂柱,装置简单易操作,具有较高的经济可行性。
图1是本发明的示意图;
其中,1是电解池;2是树脂柱;3是喷淋塔。
下面结合具体实施例对本发明进一步进行描述。
实施例1
根据下述实施例,可以更好地理解本发明。然而,本领域的技术人员容易理解,实施例中
所描述的内容仅用于说明本发明,而不应当也不会限制本发明。
实施例1:
(1)将1BV质量浓度为5%NaCl溶液在电化学反应器中以5V直流电压恒电压进行电解10min后,得到电解液,电化学反应器中阳极-阴极为钌铱钛-钛基钴氧化物电极对,阴极与阳 极面积比为1:1;
(2)将上述电解液以0.5BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以5mA/cm
2的工作电流密度进行电化学反应0.3小时后,得到流出液,该流出液作为再生液,再以0.5BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行3h后停止反应。
吸附脱附液中硝酸盐氮含量为119mg/L的
A520E树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为11mg/L,硝酸盐氮的去除率可达到90±3%。再生后的树脂再去吸附,5次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的86±2%,再生后的树脂的圆球率为77±3%,比初始树脂圆球率只降低了11%,树脂结构未发生明显变化。
实施例2:
(1)将5BV质量浓度为15%NaCl溶液在电化学反应器中以20V直流电压恒电压进行电解10min后,得到电解液,电化学反应器中阳极-阴极为钌铱钛-钛基铜/钴氧化物电极对,阴极与阳极面积比为1:0.8;
(2)将上述电解液以2BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以40mA/cm
2的工作电流密度进行电化学反应3小时后,得到流出液,该流出液作为再生液,再以2BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行5h后停止反应。
吸附脱附液中硝酸盐氮含量为1022mg/L,TOC为26mg/L的
A520E树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中TOC为1mg/L,硝酸盐氮浓度为 18mg/L,TOC去除率可达到96±3%,硝酸盐氮的去除率可达到98±3%。再生后的树脂再去吸附,8次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的75±3%,再生后的树脂的圆球率为71±2%,比初始树脂圆球率只降低了17%,树脂结构未发生明显变化。
实施例3:
(1)将1BV质量浓度为3%NaCl溶液在电化学反应器中以5V直流电压恒电压进行电解5min后,得到电解液,电化学反应器中阳极-阴极为钌铱钛-钴电极对,阴极与阳极面积比为1:1.2;
(2)将上述电解液以5BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以10mA/cm
2的工作电流密度进行电化学反应0.5小时后,得到流出液,该流出液作为再生液,再以5BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行1h后停止反应。
吸附脱附液中硝酸盐氮含量为44mg/L的
D201树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为5mg/L,硝酸盐氮的去除率可达到88±2%。再生后的树脂再去吸附,6次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的87±3%,再生后的树脂的圆球率为83±2%,比初始树脂圆球率只降低了5%,树脂结构未发生明显变化。
实施例4:
(1)将2BV质量浓度为5%NaCl溶液在电化学反应器中以3V直流电压恒电压进行电解10min后,得到电解液,电化学反应器中阳极-阴极为掺硼金刚石-钛基铜/钴氧化物电极对,阴极与阳极面积比为1:1.5;
(2)将上述电解液以6BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以15mA/cm
2的工作电流密度进行电化学反应1小时后,得到流出液,该流出液作为再生液,再以6BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行2h后停止反应。
吸附脱附液中硝酸盐氮含量为57mg/L的
D201树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为6mg/L,硝酸盐氮的去除率可达到89±2%。再生后的树脂再去吸附,5次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的90±2%,再生后的树脂的圆球率为81±3%,比初始树脂圆球率只降低了7%,树脂结构未发生明显变化。
实施例5:
(1)将5BV质量浓度为10%NaCl溶液在电化学反应器中以20V直流电压恒电压进行电解15min后,得到电解液,电化学反应器中阳极-阴极为掺硼金刚石-钛基铜/钴氧化物电极对,阴极与阳极面积比为1:0.5;
(2)将上述电解液以2.5BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以80mA/cm
2的工作电流密度进行电化学反应2小时后,得到流出液,该流出液作为再生液,再以2.5BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行4h后停止反应。
吸附脱附液中硝酸盐氮含量为813mg/L的
IRA-900树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为13mg/L,硝酸盐氮的去除率可达到98±3%。再生后的树脂再去吸附,4次吸附-再生循环后树脂再吸附的吸附量能达到再生前树 脂饱和吸附量的84±1%,再生后的树脂的圆球率为74±3%,比初始树脂圆球率只降低了14%,树脂结构未发生明显变化。
实施例6:
(1)将4BV质量浓度为8%NaCl溶液在电化学反应器中以15V直流电压恒电压进行电解10min后,得到电解液,电化学反应器中阳极-阴极为钌铱钛-钛基铜/钴氧化物电极对,阴极与阳极面积比为1:2;
(2)将上述电解液以8BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以60mA/cm
2的工作电流密度进行电化学反应2小时后,得到流出液,该流出液作为再生液,再以8BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行3.5h后停止反应。
吸附脱附液中硝酸盐氮含量为482mg/L的
IRA-900树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为15mg/L,硝酸盐氮的去除率可达到96±1%。再生后的树脂再去吸附,5次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的82±2%,再生后的树脂的圆球率为78±3%,比初始树脂圆球率只降低了10%,树脂结构未发生明显变化。
实施例7:
(1)将1.5BV质量浓度为8%NaCl溶液在电化学反应器中以10V直流电压恒电压进行电解8min后,得到电解液,电化学反应器中阳极-阴极为钌铱钛-钛基铜/钴氧化物电极对,阴极与阳极面积比为1:1.8;
(2)将上述电解液以3BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的
离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以30mA/cm
2的工作电流密度进行电化学反应1.5小时后,得到流出液,该流出液作为再生液,再以3BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行2h后停止反应。
吸附脱附液中硝酸盐氮含量为225mg/L的
A520E树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为14mg/L,硝酸盐氮的去除率可达到94±3%。再生后的树脂再去吸附,6次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的85±2%,再生后的树脂的圆球率为80±2%,比初始树脂圆球率只降低了6%,树脂结构未发生明显变化。
实施例8:
(1)将1.5BV质量浓度为8%NaCl溶液在电化学反应器中以10V直流电压恒电压进行电解15min后,得到电解液,电化学反应器中阳极-阴极为钌铱钛-钛基钴氧化物电极对,阴极与阳极面积比为1:1.8;
(2)将上述电解液以3BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以50mA/cm
2的工作电流密度进行电化学反应1.5小时后,得到流出液,该流出液作为再生液,再以3BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行2h后停止反应。
吸附脱附液中硝酸盐氮含量为177mg/L的
D202树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为10mg/L,硝酸盐氮的去除率可达到94±3%。再生后的树脂再去吸附,5次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的83±4%,再生后的树脂的圆球率为78±2%,比初始树脂圆球率只降低了9%, 树脂结构未发生明显变化。
实施例9:
(1)将4BV质量浓度为12%NaCl溶液在电化学反应器中以10V直流电压恒电压进行电解10min后,得到电解液,电化学反应器中阳极-阴极为钌铱钛-钛基铜/钴氧化物电极对,阴极与阳极面积比为1:1;
(2)将上述电解液以4BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以20mA/cm
2的工作电流密度进行电化学反应3小时后,得到流出液,该流出液作为再生液,再以4BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行4h后停止反应。
吸附脱附液中硝酸盐氮含量为598mg/L的
D202树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为9mg/L,硝酸盐氮的去除率可达到99±3%。再生后的树脂再去吸附,6次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的82±3%,再生后的树脂的圆球率为73±3%,比初始树脂圆球率只降低了13%,树脂结构未发生明显变化。
实施例10:
(1)将1BV质量浓度为10%NaCl溶液在电化学反应器中以10V直流电压恒电压进行电解15min后,得到电解液,电化学反应器中阳极-阴极为钌铱钛-钛基铜/钴氧化物电极对,阴极与阳极面积比为1:1;
(2)将上述电解液以1BV/h的流速从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;
(3)上述树脂脱附液通入喷淋塔中,与电解反应时产生的氯气进行传质反应;
(4)将传质反应后的树脂脱附液通入电化学反应器中,调整电化学反应器为恒电流电解模式,在水力搅拌条件下以20mA/cm
2的工作电流密度进行电化学反应1小时后,得到流出液,该流出液作为再生液,再以1BV/h的流速从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液通入电化学反应器中进行电化学反应,如此进行循环反应。
(5)整个树脂再生过程进行2.5h后停止反应。
吸附脱附液中硝酸盐氮含量为641mg/L,TOC为22mg/L的
IRA-900树脂,经过上述电解盐溶液高效再生树脂的方法处理后,流出液中硝酸盐氮浓度为9mg/L、TOC为0.4mg/L,硝酸盐氮的去除率可达到99±3%,有机物去除率可达到98±3%。再生后的树脂再去吸附,5次吸附-再生循环后树脂再吸附的吸附量能达到再生前树脂饱和吸附量的80±3%,再生后的树脂的圆球率为72±2%,比初始树脂圆球率只降低了16%,树脂结构未发生明显变化。
需要说明的是,以上实施例仅用以说明本发明的技术方案而非限制。尽管参照较佳实施例对本发明进行了详细说明,本领域的普通技术人员应当理解,可以对发明的技术方案进行修改或者等同替换,而不脱离本发明技术方案的范围,其均应涵盖在本发明的权利要求范围中。
Claims (10)
- 一种电解盐溶液高效再生树脂的方法,其特征在于,它包括以下步骤:(1)将质量浓度为1~20%NaCl溶液以1~30V电压进行电解反应后,得到电解液;(2)将所述电解液从填充有离子交换树脂的树脂柱底部通入,对填充的离子交换树脂进行反洗后,得到树脂脱附液;(3)将所述树脂脱附液进行电化学反应后,得到流出液,所述流出液从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液进行电化学反应,如此进行循环反应。
- 根据权利要求1所述的电解盐溶液高效再生树脂的方法,其特征在于,将步骤(2)得到的树脂脱附液先通入喷淋塔中,与步骤(1)中电解反应时产生的氯气进行传质反应,传质反应后的树脂脱附液再进行电化学反应,得到液出液,所述流出液从树脂柱底部通入,对填充的离子交换树脂进行反洗,反洗后的废液进行电化学反应,如此进行循环反应。
- 根据权利要求1或2所述的电解盐溶液高效再生树脂的方法,其特征在于,在电化学反应器中进行电化学反应,所述电化学反应器包括阳极和阴极,其中,阳极-阴极为钌铱钛-铜、钌铱钛-钴、钌铱钛-钛基钴氧化物、钌铱钛-铜镍合金、钌铱钛-钛基铜/钴氧化物、钌铱钛-铂、石墨-铁、掺硼金刚石-铜镍合金或掺硼金刚石-钛基铜/钴氧化物;优选为钌铱钛-钛基铜/钴氧化物、钌铱钛-钛基钴氧化物或掺硼金刚石-钛基铜/钴氧化物。
- 根据权利要求3所述的电解盐溶液高效再生树脂的方法,其特征在于,阴极与阳极的面积比为1:0.1~1:2.5;优选为1:0.5~1:2。
- 根据权利要求1或2所述的电解盐溶液高效再生树脂的方法,其特征在于,进行电化学反应时的电流密度为3~150mA/cm 2;优选为5~100mA/cm 2;电化学反应时间为0.3~3h,优选为0.5~2h。
- 根据权利要求1或2所述的电解盐溶液高效再生树脂的方法,其特征在于,在步骤(1)中,NaCl溶液的用量为1~5BV;优选为1.5~3BV;NaCl溶液的质量浓度为5~10%。
- 根据权利要求1或2所述的电解盐溶液高效再生树脂的方法,其特征在于,在步骤(1)中,电解反应的电压为5~20V;电解反应的时间为5~15min。
- 根据权利要求1或2所述的电解盐溶液高效再生树脂的方法,其特征在于,电解液从树脂柱底部通入的流速为0.1~10BV/h;优选为0.2~5BV/h;流出液从树脂柱底部通入的流速为0.1~10BV/h;优选为0.2~5BV/h。
- 根据权利要求1或2所述的电解盐溶液高效再生树脂的方法,其特征在于,在整个再生反应进行1~5h后停止反应,更换树脂柱,继续步骤(2)。
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