WO2018233610A1 - 一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法 - Google Patents
一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法 Download PDFInfo
- Publication number
- WO2018233610A1 WO2018233610A1 PCT/CN2018/091851 CN2018091851W WO2018233610A1 WO 2018233610 A1 WO2018233610 A1 WO 2018233610A1 CN 2018091851 W CN2018091851 W CN 2018091851W WO 2018233610 A1 WO2018233610 A1 WO 2018233610A1
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- WIPO (PCT)
- Prior art keywords
- fly ash
- chromium slag
- waste incineration
- chromium
- leachate
- Prior art date
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- 239000010881 fly ash Substances 0.000 title claims abstract description 88
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 title claims abstract description 83
- 229910052804 chromium Inorganic materials 0.000 title claims abstract description 68
- 239000011651 chromium Substances 0.000 title claims abstract description 68
- 239000002893 slag Substances 0.000 title claims abstract description 62
- 238000000034 method Methods 0.000 title claims abstract description 48
- 238000004056 waste incineration Methods 0.000 title claims description 35
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 52
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 52
- 235000020939 nutritional additive Nutrition 0.000 claims abstract description 31
- 235000003891 ferrous sulphate Nutrition 0.000 claims abstract description 30
- 239000011790 ferrous sulphate Substances 0.000 claims abstract description 30
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims abstract description 30
- 229910000359 iron(II) sulfate Inorganic materials 0.000 claims abstract description 30
- 239000000463 material Substances 0.000 claims abstract description 23
- 238000005507 spraying Methods 0.000 claims abstract description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 239000007787 solid Substances 0.000 claims description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 10
- 239000011701 zinc Substances 0.000 claims description 10
- 229910052725 zinc Inorganic materials 0.000 claims description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 9
- 239000010815 organic waste Substances 0.000 claims description 8
- 239000011573 trace mineral Substances 0.000 claims description 8
- 235000013619 trace mineral Nutrition 0.000 claims description 8
- 229910017112 Fe—C Inorganic materials 0.000 claims description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- 239000011574 phosphorus Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 239000002699 waste material Substances 0.000 claims description 5
- 229910052742 iron Inorganic materials 0.000 claims description 4
- 239000010802 sludge Substances 0.000 claims description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052796 boron Inorganic materials 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 3
- 235000015097 nutrients Nutrition 0.000 claims description 3
- 238000010979 pH adjustment Methods 0.000 claims description 3
- 230000003134 recirculating effect Effects 0.000 claims description 3
- 239000002689 soil Substances 0.000 claims description 3
- 239000003575 carbonaceous material Substances 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 claims description 2
- 239000008187 granular material Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000000706 filtrate Substances 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 238000005868 electrolysis reaction Methods 0.000 abstract description 15
- 239000000203 mixture Substances 0.000 abstract description 11
- 230000008569 process Effects 0.000 abstract description 4
- 238000010169 landfilling Methods 0.000 abstract 1
- 230000003247 decreasing effect Effects 0.000 description 34
- 239000000243 solution Substances 0.000 description 32
- KVGZZAHHUNAVKZ-UHFFFAOYSA-N 1,4-Dioxin Chemical compound O1C=COC=C1 KVGZZAHHUNAVKZ-UHFFFAOYSA-N 0.000 description 18
- 239000010806 kitchen waste Substances 0.000 description 14
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 14
- 229910001385 heavy metal Inorganic materials 0.000 description 13
- 239000000460 chlorine Substances 0.000 description 10
- 238000010992 reflux Methods 0.000 description 9
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 description 8
- 238000004090 dissolution Methods 0.000 description 8
- -1 iron ions Chemical class 0.000 description 8
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 7
- UFMZWBIQTDUYBN-UHFFFAOYSA-N cobalt dinitrate Chemical compound [Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O UFMZWBIQTDUYBN-UHFFFAOYSA-N 0.000 description 7
- 229910001981 cobalt nitrate Inorganic materials 0.000 description 7
- 150000002013 dioxins Chemical class 0.000 description 7
- 229910052745 lead Inorganic materials 0.000 description 7
- 244000005700 microbiome Species 0.000 description 7
- 239000002957 persistent organic pollutant Substances 0.000 description 7
- 229910000160 potassium phosphate Inorganic materials 0.000 description 7
- 235000011009 potassium phosphates Nutrition 0.000 description 7
- 239000002910 solid waste Substances 0.000 description 7
- 239000000356 contaminant Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000005416 organic matter Substances 0.000 description 6
- 230000009471 action Effects 0.000 description 5
- 239000002994 raw material Substances 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000002920 hazardous waste Substances 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229920002521 macromolecule Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 150000003384 small molecules Chemical class 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000005842 biochemical reaction Methods 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000000185 dioxinlike effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010335 hydrothermal treatment Methods 0.000 description 1
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 230000007269 microbial metabolism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B09—DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
- B09B—DISPOSAL OF SOLID WASTE NOT OTHERWISE PROVIDED FOR
- B09B3/00—Destroying solid waste or transforming solid waste into something useful or harmless
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B09—DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
- B09B—DISPOSAL OF SOLID WASTE NOT OTHERWISE PROVIDED FOR
- B09B1/00—Dumping solid waste
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/467—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction
- C02F1/4672—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction by electrooxydation
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B34/00—Obtaining refractory metals
- C22B34/30—Obtaining chromium, molybdenum or tungsten
- C22B34/32—Obtaining chromium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/02—Working-up flue dust
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/04—Working-up slag
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J1/00—Removing ash, clinker, or slag from combustion chambers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B09—DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
- B09B—DISPOSAL OF SOLID WASTE NOT OTHERWISE PROVIDED FOR
- B09B2101/00—Type of solid waste
- B09B2101/30—Incineration ashes
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/46104—Devices therefor; Their operating or servicing
- C02F1/4618—Devices therefor; Their operating or servicing for producing "ionised" acidic or basic water
- C02F2001/46185—Devices therefor; Their operating or servicing for producing "ionised" acidic or basic water only anodic or acidic water, e.g. for oxidizing or sterilizing
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/20—Heavy metals or heavy metal compounds
- C02F2101/22—Chromium or chromium compounds, e.g. chromates
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/06—Contaminated groundwater or leachate
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/16—Nature of the water, waste water, sewage or sludge to be treated from metallurgical processes, i.e. from the production, refining or treatment of metals, e.g. galvanic wastes
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2305/00—Use of specific compounds during water treatment
- C02F2305/02—Specific form of oxidant
- C02F2305/026—Fenton's reagent
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2700/00—Ash removal, handling and treatment means; Ash and slag handling in pulverulent fuel furnaces; Ash removal means for incinerators
- F23J2700/003—Ash removal means for incinerators
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- the present application relates to the field of environmental protection technologies, and in particular, to a method for co-processing waste incineration fly ash and chromium slag in a landfill.
- Waste incineration fly ash is classified as hazardous waste due to its high concentration of heavy metals and dioxin-like POPs.
- chromium slag is also a kind of hazardous waste.
- the main treatment method of fly ash and chromium slag is landfill, but landfill occupies a large amount of land, and in the process of fly ash transport and open-air landfill, it is easy to form floating dust into the atmosphere, not only Increase the dust content in the air, and may increase the ecological toxicity of smog, cause serious pollution to the atmosphere, and endanger the health and ecological environment of residents.
- the present application proposes a method for co-processing waste incineration fly ash and chromium slag in a landfill, and through special biochemical and engineering measures in the landfill process to improve the above technical problems.
- a method for co-processing waste incineration fly ash and chromium slag in a landfill comprising:
- the anti-seepage layer is laid in the yard for the disposal of fly ash and chromium slag, and the flow guiding material is laid at the bottom, and the upper layer includes a mixed layer of biogas residue, carbon source, ferrous sulfate, nutritional additive, fly ash and chromium slag.
- the inner electrolysis ceramsite layer is placed on the upper part of the mixed layer; during the operation, the carbon source solution is injected from the upper part of the stack from time to time, and the leachate is collected from the bottom diversion material to the leachate collection system from time to time, and then the leachate is returned to the heap.
- the top of the field is sprayed and recharged.
- fly ash, chromium slag, biogas residue, carbon source, ferrous sulfate and nutritional additives in the mixed layer are added in a mass ratio of 1: (0.1-10): (0.01-5): (0.01-5) :(0.15-3): (0.1-1).
- the thickness of the mixed layer is 1-8 m; the thickness of the inner electrolytic ceramsite layer does not exceed 1 m.
- the spraying interval of the leachate refluxing to the top of the stack for spraying and refilling is 1-48 hours.
- the leachate is refluxed to the top of the stack to perform pH adjustment on the leachate, so that the pH of the recirculated leachate is 2-5.
- biogas residue includes organic wastewater, solid organic waste or sludge.
- biogas residue is a solid organic waste after anaerobic treatment.
- the frequency of the carbon source solution in the upper portion of the yard is once every 1-100 days.
- the nutritional additive includes one or more of a nitrogen source, a phosphorus source, and a trace element source.
- the carbon source mass percentage in the carbon source solution is not more than 50%.
- the trace element source includes a nutrient containing one or more elements of boron, zinc, copper, manganese, and cobalt.
- the carbon source solution includes a solution containing one or more of ethanol, methanol, and acetic acid.
- the carbon source solution is doped with ferrous sulfate.
- fly ash includes fly ash after biochemical, physical or chemical disposal.
- the chromium slag includes chromium-containing soil or chromium-containing waste.
- the inner electrolytic ceramsite layer is placed inside the electrolytic ceramsite.
- Internal electrolysis ceramsite also known as microelectrolytic ceramsite, can spontaneously generate electricity under certain conditions.
- the internal electrolysis ceramsite of the internal electrolysis ceramsite layer is Fe-C type internal electrolysis ceramsite, and the internal electrolysis ceramsite contains Fe metal and carbon material, which can generate endogenous current under acidic conditions.
- the mechanism of the method for treating heavy metals and dioxins in fly ash is that first, ferrous sulfate reduces hexavalent chromium in the chromium slag, and then the sulfate reducing bacteria in the biogas residue converts the sulfate in the ferrous sulfate into a sulphate by using a carbon source. Sulfide, heavy metal reacts with sulfide to form a very low solubility precipitate, which greatly reduces the amount of dissolution, while further detoxifying the untreated chromium residue.
- the dioxin in the fly ash is extracted into the leachate by using the carbon source solution and the organic matter degraded by the microorganism residue, and the leachate is recharged to the top of the yard, and the electricity is formed by the action of the internal electrolysis ceramsite.
- the catalytic effect produces hydroxyl radicals and further promotes the decomposition of dioxins.
- the leachate contains the eluate of the biogas residue, which contains a large amount of macromolecular organic matter such as microbial residues, which is difficult to be bio-utilized, so that the biochemical property is not strong, and it flows back to the top of the mixed landfill. Under the action of the granules, the macromolecules are converted into small molecules, which improves the biodegradability. Then, the part of the leachate enters the mixed layer, which is better utilized by the microorganisms in the biogas residue, and accelerates the biodegradation of the biogas residue as a whole.
- the fly ash contains a large amount of Cl.
- the Cl ion in the leachate is converted into Cl 2 and left the landfill by internal electrolysis, thereby reducing the chlorine content in the landfill.
- the production of Cl 2 will also disinfect the harmful microorganisms in the landfill.
- This method can improve the negative impact of waste incineration fly ash and chromium slag on the environment.
- FIG. 1 is a schematic view showing a method for co-processing waste incineration fly ash and chromium slag in a landfill in the present application.
- Icons 1-acid addition device; 2-electrolytic ceramsite layer; 3-impermeable layer; 4-mixed layer; 5-flow material; 6-leachate storage tank.
- Fig. 1 is a schematic view showing a method for co-processing waste incineration fly ash and chromium slag in a landfill in the present application.
- a method for co-processing waste incineration fly ash and chromium slag in a landfill includes laying an anti-seepage layer 3 in a yard for disposal of fly ash and chromium slag, bottom portion
- the flow guiding material 5 is laid, and the mixed layer 4 including the biogas residue, the carbon source, the ferrous sulfate, the nutritional additive, the fly ash and the chromium residue is laid on the upper part, and the inner electrolytic ceramic layer 2 is placed on the upper part of the mixed layer 4.
- the fly ash, chromium slag, biogas residue, carbon source, ferrous sulfate and nutritional additives in the mixed layer 4 are added in a mass ratio of 1: (0.1-10): (0.01-5): (0.01-5) :(0.15-3): (0.1-1).
- the thickness of the mixed layer 4 is 1-8 m; the thickness of the inner electrolytic ceramsite layer 2 does not exceed 1 m.
- the biogas residue can be selected from organic wastewater, solid organic waste or sludge, and the solid organic waste can be used as an anaerobic treatment and then as a biogas residue.
- the nutritive additive includes one or more of a nitrogen source, a phosphorus source and a trace element source, and the addition of the phosphorus source, the nitrogen source and the trace element further promotes the activity of the microorganism in the biogas residue and enhances the disposal of the persistent organic pollutant ( Persistent Organic Pollutants, referred to as POPs).
- the trace element source may be selected to include a nutrient containing one or more elements of boron, zinc, copper, manganese, and cobalt.
- Fly ash includes untreated waste incineration fly ash or fly ash after biochemical, physical or chemical disposal. For example, fly ash after heat treatment, hydrothermal treatment, and chemical stabilization treatment.
- the chromium slag of the examples of the present application may include chromium-containing soil or chromium-containing waste.
- the carbon source solution includes a solution containing one or more of ethanol, methanol, and acetic acid, which can be used as both a microbial carbon source and a POP, such as dioxins in the fly ash.
- the carbon source solution is optionally doped with ferrous sulfate, and the carbon source has a carbon source mass percentage of not more than 50%.
- the spraying interval of the leachate refluxing to the top of the stack for spraying and refilling is 1-48 hours.
- the leachate can be adjusted to pH so that the pH of the recirculated leachate is 2-5, and the pH can be adjusted by adding the acid device 1.
- the micro-electrolytic ceramsite will release a certain amount of iron ions, which will produce a Fenton catalytic effect under the action of a trace amount of hydroxyl radical generated by electrocatalysis, effectively degrading dioxin pollution, and at the same time
- the refractory organic matter produced by the biogas residue is removed.
- the frequency of carbon injection solution in the upper part of the yard is once every 1-100 days.
- Ferrous Sulfate Detoxifies chromium slag at the same time, releases iron and sulfate, iron can be used as raw material of Fenton effect, and sulfate is used as raw material of sulfate reducing bacteria in biogas residue to further participate in the next biochemical reaction.
- the sulfate reducing bacteria in the biogas residue fully utilizes the ferrous sulfate to immobilize the heavy metal, which is ecologically safe compared with the direct use of the chemical curing agent to fix the heavy metal.
- POPs Persistent Organic Pollutants
- the leachate contains the leachate of the biogas residue, which contains a large amount of macromolecular organic matter such as microbial residues, which is difficult to be bio-utilized, so that the biochemical property is not strong, and it flows back to the top of the mixed landfill. Under the action of electrolytic ceramsite, macromolecules are converted into small molecules, which improves biodegradability. Then, this part of the leachate enters the mixed layer, which is better utilized by microorganisms in the biogas residue, and accelerates the biogas residue organism as a whole. degradation.
- the fly ash contains a large amount of Cl.
- the Cl ion in the leachate is converted into Cl 2 and left the landfill by internal electrolysis, thereby reducing the chlorine content in the landfill.
- the production of Cl 2 will also disinfect the harmful microorganisms in the landfill.
- the acid added to the internal electrolysis ceramsite can be used as an important raw material for the operation of internal electrolysis ceramsite, or as a raw material for neutralizing high-alkaline hazardous waste such as chromium slag and fly ash, so that the landfill tends to neutral.
- the present embodiment provides a method for co-processing waste incineration fly ash and chromium slag in a landfill, the method comprising transferring fly ash and chromium slag into a yard; laying an anti-seepage layer 3 in the yard, laying a bottom guide
- the flow material 5 is provided with a mixed layer of biogas residue, carbon source, ferrous sulfate, nutritional additive, fly ash and chromium slag on the upper part thereof, and the carbon source is selected as kitchen waste.
- the addition ratio of fly ash, chromium residue, biogas residue, kitchen waste, ferrous sulfate and nutritional additives is 1:0.5:0.2:0.2:0.15:0.1
- the thickness of the mixed layer 4 is 5m
- the mixed layer 4 The inner electrolytic ceramsite is placed in the upper part and has a thickness of 0.1 m.
- the carbon source solution is injected from the upper part of the stack every 1-5 days.
- the carbon source solution is an ethanol solution.
- the leachate is then collected through the bottom flow guiding material 5 into the leachate collection system, and then the leachate is returned to the upper portion of the yard for recirculation every 1 day, and the pH is adjusted to 4 before reflux.
- the solid hexavalent chromium content in the yard decreased from 3000mg/kg to less than 2mg/kg, the dissolution rate of heavy metals in solid waste in the yard decreased by 91%, and Pb decreased from 5mg/L to less than 0.1mg/L.
- the Cd decreased from 3 mg/L to less than 0.1 mg/L, while the removal rate of dioxin and other contaminants exceeded 99%, and the dioxin content reached the standard.
- the nutritional additive of the present example is a mixture of potassium phosphate, ammonium nitrate and cobalt nitrate, and a trace amount of zinc element is added, and the internal electrolytic ceramsite is Fe-C type internal electrolytic ceramsite.
- the present embodiment provides a method for co-processing waste incineration fly ash and chromium slag in a landfill, the method comprising transferring fly ash and chromium slag into a yard; laying an anti-seepage layer 3 in the yard, laying a bottom guide
- the flow material 5 is provided with a mixed layer of biogas residue, carbon source, ferrous sulfate, nutritional additive, fly ash and chromium slag on the upper part thereof, and the carbon source is selected as kitchen waste.
- the addition ratio of fly ash, chromium residue, biogas residue, kitchen waste, ferrous sulfate and nutritional additives is 1:2:0.5:0.4:0.3:0.1
- the thickness of the mixed layer 4 is 5m
- the mixed layer 4 The inner electrolytic ceramsite is placed in the upper part and has a thickness of 0.01 m.
- the ethanol solution is injected from the upper part of the stack every 30 days, and then the leachate is collected into the leachate collection system through the bottom flow guiding material 5, and then every interval 2
- the leachate is returned to the upper part of the yard for recirculation, and the pH is adjusted to 4 before reflux.
- the solid hexavalent chromium content in the yard decreased from 3000mg/kg to less than 2mg/kg
- the dissolution rate of heavy metals in solid waste in the yard decreased by 91%
- Pb decreased from 5mg/L to less than 0.1mg/L.
- the Cd decreased from 3 mg/L to less than 0.1 mg/L
- the pollutants such as dioxins decreased from 500 ng/kg to 8 ng/kg, the removal rate exceeded 99%
- the dioxin content reached the standard.
- the leachate COD decreased from over 10,000 mg/L to less than 200 mg/L.
- the nutritional additive of the present example is a mixture of potassium phosphate, ammonium nitrate and cobalt nitrate, and a trace amount of zinc element is added, and the internal electrolytic ceramsite is Fe-C type internal electrolytic ceramsite.
- the present embodiment provides a method for co-processing waste incineration fly ash and chromium slag in a landfill, the method comprising transferring fly ash and chromium slag into a yard; laying an anti-seepage layer 3 in the yard, laying a bottom guide
- the flow material 5 is provided with a mixed layer of biogas residue, carbon source, ferrous sulfate, nutritional additive, fly ash and chromium slag on the upper part thereof, and the carbon source is selected as kitchen waste.
- the addition ratio of fly ash, chromium residue, biogas residue, kitchen waste, ferrous sulfate and nutritional additives is 1:1.5:0.5:0.4:0.2:0.1, the thickness of the mixed layer 4 is 5m, the mixed layer 4
- the inner electroceramic layer 2 is not disposed on the upper part; during the operation, the ethanol solution is injected from the upper part of the yard every 25 days, and then the leachate is collected into the leachate collection system through the bottom flow guiding material 5, and then every 2 days interval The leachate is returned to the upper part of the yard for recharge, and the pH is adjusted to 4 before reflux.
- the solid hexavalent chromium content in the yard decreased from 3000mg/kg to less than 2mg/kg.
- the dissolution rate of heavy metals in solid waste in the yard decreased by 91%, and Pb decreased from 5mg/L to less than 0.1mg/L.
- the Cd decreased from 3 mg/L to less than 0.1 mg/L, while the removal rate of dioxin and other contaminants exceeded 99%, and the dioxin content reached the standard.
- the leachate COD decreased from more than 10,000 mg/L to less than 500 mg/L.
- the nutritional additive of this example is a mixture of potassium phosphate, ammonium nitrate and cobalt nitrate, while adding a trace amount of zinc.
- the fly ash and chromium slag are transferred to the yard; the anti-seepage layer 3 is laid in the yard, the flow guiding material 5 is laid at the bottom, and the upper part is laid with sludge, carbon source, ferrous sulfate, nutritional additives, fly ash and chromium slag.
- Mixed layer 4 the carbon source is selected as kitchen waste. According to the mass, the addition ratio of fly ash, chromium residue, biogas residue, kitchen waste, ferrous sulfate and nutritional additives is 1:2:0.5:0.4:0.3:0.1, the thickness of the mixed layer 4 is 5m, the mixed layer 4
- the inner electrolytic ceramsite is placed in the upper part and has a thickness of 0.01 m.
- a mixture of the ethanol solution and the ferrous sulfate is injected from the upper part of the stack every 30 days, and then the leachate is collected through the bottom flow guiding material 5 to the leachate collection.
- the leachate is then returned to the upper part of the yard for recirculation every 2 days, and the pH is adjusted to 4 before reflux.
- the solid hexavalent chromium content in the yard decreased from 3000mg/kg to less than 2mg/kg.
- the dissolution rate of heavy metals in solid waste in the yard decreased by 91%, and Pb decreased from 5mg/L to less than 0.1mg/L.
- the Cd decreased from 3 mg/L to less than 0.1 mg/L, while the removal rate of dioxin and other contaminants exceeded 99%, and the dioxin content reached the standard.
- the leachate COD decreased from over 10,000 mg/L to less than 300 mg/L.
- the nutritional additive of this example is a mixture of potassium phosphate, ammonium nitrate and cobalt nitrate, while adding a trace amount of zinc.
- the present embodiment provides a method for co-processing waste incineration fly ash and chromium slag in a landfill, the method comprising transferring fly ash and chromium slag into a yard; laying an anti-seepage layer 3 in the yard, laying a bottom guide
- the flow material 5 is provided with a mixed layer of biogas residue, carbon source, ferrous sulfate, nutritional additive, fly ash and chromium slag on the upper part thereof, and the carbon source is selected as kitchen waste.
- the addition ratio of fly ash, chromium residue, biogas residue, kitchen waste, ferrous sulfate and nutritional additives is 1:6:2:2:1.5:0.5
- the thickness of the mixed layer 4 is 5m
- the mixed layer 4 The inner electrolytic ceramsite is placed in the upper part and has a thickness of 0.1 m.
- the carbon source solution is injected from the upper part of the stack every 70 days.
- the carbon source solution is a methanol solution.
- the leachate is then collected through the bottom flow guiding material 5 into the leachate collection system, and then the leachate is returned to the upper portion of the stack for reflow every 1 hour, and the pH is adjusted to 2 before reflux.
- the solid hexavalent chromium content in the yard decreased from 3000mg/kg to less than 2mg/kg, the dissolution rate of heavy metals in solid waste in the yard decreased by 91%, and Pb decreased from 5mg/L to less than 0.1mg/L.
- the Cd decreased from 3 mg/L to less than 0.1 mg/L, while the removal rate of dioxin and other contaminants exceeded 99%, and the dioxin content reached the standard.
- the leachate COD decreased from more than 10,000 mg/L to less than 100 mg/L.
- the nutritional additive of this example is a mixture of potassium phosphate, ammonium nitrate and cobalt nitrate, with the addition of trace amounts of zinc.
- the present embodiment provides a method for co-processing waste incineration fly ash and chromium slag in a landfill, the method comprising transferring fly ash and chromium slag into a yard; laying an anti-seepage layer 3 in the yard, laying a bottom guide
- the flow material 5 is provided with a mixed layer of biogas residue, carbon source, ferrous sulfate, nutritional additive, fly ash and chromium slag on the upper part thereof, and the carbon source is selected as kitchen waste.
- the addition ratio of fly ash, chromium residue, biogas residue, kitchen waste, ferrous sulfate and nutritional additives is 1:3.5:2:2.5:2:0.5
- the thickness of the mixed layer 4 is 1m
- the mixed layer 4 The inner electrolytic ceramsite is placed in the upper part and has a thickness of 0.6 m.
- the carbon source solution is injected from the upper part of the stack every 100 days.
- the carbon source solution is an acetic acid solution.
- the leachate is then collected through the bottom flow guiding material 5 into the leachate collection system, and then the leachate is returned to the upper portion of the yard for recirculation every 2 days, and the pH is adjusted to 5 before reflux.
- the solid hexavalent chromium content in the yard decreased from 3000mg/kg to less than 2mg/kg, the dissolution rate of heavy metals in solid waste in the yard decreased by 91%, and Pb decreased from 5mg/L to less than 0.1mg/L.
- the Cd decreased from 3 mg/L to less than 0.1 mg/L, while the removal rate of dioxin and other contaminants exceeded 99%, and the dioxin content reached the standard.
- the nutritional additive of this example is a mixture of potassium phosphate, ammonium nitrate and cobalt nitrate, while adding a trace amount of zinc.
- the present embodiment provides a method for co-processing waste incineration fly ash and chromium slag in a landfill, the method comprising transferring fly ash and chromium slag into a yard; laying an anti-seepage layer 3 in the yard, laying a bottom guide
- the flow material 5 is provided with a mixed layer of biogas residue, carbon source, ferrous sulfate, nutritional additive, fly ash and chromium slag on the upper part thereof, and the carbon source is selected as kitchen waste.
- the addition ratio of fly ash, chromium residue, biogas residue, kitchen waste, ferrous sulfate and nutritional additives is 1:10:5:5:3:1, the thickness of mixed layer 4 is 8m, mixed layer 4
- the inner electrolytic ceramsite is placed in the upper part and has a thickness of 1 m.
- the carbon source solution is injected from the upper part of the stack every 30 days.
- the carbon source solution is a mixture of a methanol solution and a ferrous sulfate.
- the leachate is then collected through the bottom flow guiding material 5 into the leachate collection system, and then the leachate is returned to the upper portion of the yard for recirculation every 1 day, and the pH is adjusted to 4 before reflux.
- the solid hexavalent chromium content in the yard decreased from 3000mg/kg to less than 2mg/kg, the dissolution rate of heavy metals in solid waste in the yard decreased by 91%, and Pb decreased from 5mg/L to less than 0.1mg/L.
- the Cd decreased from 3 mg/L to less than 0.1 mg/L, while the removal rate of dioxin and other contaminants exceeded 99%, and the dioxin content reached the standard.
- the leachate COD decreased from over 10,000 mg/L to less than 200 mg/L.
- the nutritional additive of this example is a mixture of potassium phosphate, ammonium nitrate and cobalt nitrate, while adding a trace amount of zinc.
- the method for co-processing waste incineration fly ash and chromium residue in the landfill of the present application can extract the dioxins in the fly ash into the solution by using the carbon source solution, and promote the dioxins by the action of the internal electrolysis ceramsite. break down.
- the heavy metal is reacted with the sulfide to form a precipitate of extremely low solubility, and the chromium residue is rendered harmless.
- the method can improve the negative impact of waste incineration fly ash and chromium slag on the environment, and rapidly degrade the organic matter content of organic waste such as biogas residue, and promote its rapid stabilization.
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Abstract
一种同步处置飞灰及铬渣的方法,在填埋过程中通过生化及工程措施,将二者无害化。将飞灰及铬渣转移到堆场中;堆场内铺设防渗层(3),底部铺设导流材料(5),其上部铺设沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层(4),混合层(4)上部放置内电解陶粒层(2);运行过程中,不定期从堆场上部注碳源溶液,不定期将渗滤液通过底部导流材料(5)收集至渗滤液收集系统中,随后将渗滤液回流至堆场顶部进行喷洒回灌。
Description
相关申请的交叉引用
本申请要求于2017年06月20日提交中国专利局的申请号为CN201710471506.4、名称为“一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法”的中国专利申请的优先权,其全部内容通过引用结合在本申请中。
本申请涉及环境保护技术领域,具体而言,涉及一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法。
垃圾焚烧飞灰因含有较高浓度的重金属、二噁英类持久性有机污染物而被列为危险废弃物。另外,铬渣也是一种危险废物,飞灰、铬渣目前的主要处理方式是填埋,但是填埋占用大量土地,并且飞灰转运及露天堆填等过程中,易形成飘尘进入大气,不仅增加空气中的粉尘含量,而且可能会加重雾霾的生态毒性,对大气造成严重污染,危害居民健康和生态环境。
发明内容
针对现有技术的不足,本申请提出一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,在填埋过程中通过特殊的生化及工程措施,以改善上述的技术问题。
本申请是通过以下方式实现的:
一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,包括:
在用于飞灰及铬渣处置的堆场内铺设防渗层,底部铺设导流材料,其上部铺设包括沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层,混合层上部放置内电解陶粒层;运行过程中,不定期从堆场上部注碳源溶液,不定期将渗滤液通过底部导流材料收集至渗滤液收集系统中,随后将渗滤液回流至堆场顶部进行喷洒回灌。
进一步的,混合层中的飞灰、铬渣、沼渣、碳源、硫酸亚铁及营养添加剂按质量计添加比例为1:(0.1-10):(0.01-5):(0.01-5):(0.15-3):(0.1-1)。
进一步的,混合层的厚度为1-8m;内电解陶粒层的厚度不超过1m。
进一步的,渗滤液回流至堆场顶部进行喷洒回灌的喷洒间隔时间为1-48小时。
进一步的,将渗滤液回流至堆场顶部进行喷洒回灌时对渗滤液进行pH调节,使回灌的渗滤液pH值为2-5。
进一步的,沼渣包括有机废水、固体有机废物或污泥。
进一步的,沼渣为经厌氧处理后的固体有机废物。
进一步的,运行期间,在堆场上部注碳源溶液的频率为每1-100天一次。
进一步的,营养添加剂包括氮源、磷源及微量元素源中的一种或多种。
进一步的,碳源溶液中碳源质量百分含量不高于50%。
进一步的,微量元素源包括含有硼、锌、铜、锰、钴中的一种或多种元素的营养物质。
进一步的,碳源溶液包括含有乙醇、甲醇、乙酸中一种或多种的溶液。
进一步的,碳源溶液掺杂有硫酸亚铁。
进一步的,飞灰包括经过生化、物理或化学处置后的飞灰。
进一步的,铬渣包括含铬土壤或含铬废物。
进一步的,内电解陶粒层放置内电解陶粒。内电解陶粒,又称微电解陶粒,其可以在特定情况下自发产生电流。
进一步的,内电解陶粒层的内电解陶粒为Fe-C型内电解陶粒,内电解陶粒中含有Fe金属及碳材料,其可以在酸性条件下产生内生电流。
本申请实施例的作用机理及有益效果是:
本方法处理飞灰中重金属及二噁英的机理在于,首先硫酸亚铁将铬渣中六价铬还原,随后沼渣中的硫酸盐还原菌利用碳源将硫酸亚铁中的硫酸盐转化为硫化物,重金属与硫化物反应生成极低溶解度的沉淀物,大大减少其溶出量,同时进一步将未处置的铬渣无害化。同时利用碳源溶液及被沼渣微生物降解后的有机物将飞灰中的二噁英萃取进入渗滤液中,随着渗滤液回灌到堆场顶部,在内电解陶粒的作用下,形成电催化效应,产生羟基自由基,进一步促进二噁英的分解。
渗滤液中包含着沼渣的溶出液,其中含有大量诸如微生物残体在内的大分子有机质,难以被生物利用,即可生化性不强,通过回流至混合填埋场顶部,在内电解陶粒的作用下,大分子转变成小分子,提高了可生化性,随后这部分渗滤液进入混合层,会更好的被沼渣中微生物获取利用,从整体上加快了沼渣的生物降解。
同时,飞灰中含有大量的Cl,进入渗滤液后,通过内电解作用,将渗滤液中Cl离子转变为Cl
2离开填埋场,从而降低填埋场中氯含量。同时Cl
2的产生也会对填埋场有害微生物进行消毒处理。
通过该方法能够改善垃圾焚烧飞灰以及铬渣对环境的负面影响。
为了更清楚地说明本申请实施例或现有技术中的技术方案,下面将对实施例描述中所需要使用的附图作简单地介绍,显而易见地,下面描述中的附图仅仅是本申请的一些实施例,对于本领域普通技术人员来讲,在不付出创造性劳动的前提下,还可以根据这些附图获得其他的附图。
图1是本申请中填埋场内协同处置垃圾焚烧飞灰及铬渣的方法的示意图。
图标:1-加酸装置;2-内电解陶粒层;3-防渗层;4-混合层;5-导流材料;6-渗滤液储存池。
为使本申请实施例的目的、技术方案和优点更加清楚,下面将对本申请实施例中的技术方案进行清楚、完整地描述。实施例中未注明具体条件者,按照常规条件或制造商建议的条件进行。所用试剂或仪器未注明生产厂商者,均为可以通过市售购买获得的常规产品。
图1是本申请中填埋场内协同处置垃圾焚烧飞灰及铬渣的方法的示意图。请参照图1,本申请实施例提供的一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,包括在用于飞灰及铬渣处置的堆场内铺设防渗层3,底部铺设导流材料5,其上部铺设包括沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层4,混合层4上部放置内电解陶粒层2。
其中,混合层4中的飞灰、铬渣、沼渣、碳源、硫酸亚铁及营养添加剂按质量计添加比例为1:(0.1-10):(0.01-5):(0.01-5):(0.15-3):(0.1-1)。混合层4的厚度为1-8m;内电解陶粒层2的厚度不超过1m。沼渣可选为有机废水、固体有机废物或污泥,其中固体有机废物可以先经过厌氧处理再作为沼渣使用。营养添加剂包括氮源、磷源及微量元素源中的一种或多种,磷源、氮源及微量元素的加入进一步促进了沼渣中微生物的活性,增强了其处置持久性有机污染物(Persistent Organic Pollutants,简称POPs)的能力。其中,微量元素源可选为包括含有硼、锌、铜、锰、钴中的一种或多种元素的营养物质。飞灰包括未经处理的垃圾焚烧飞灰或者经过生化、物理或化学处置后的飞灰。比如经过热处理、水热处理、化学药剂稳定化处理后的飞灰。本申请实施例的铬渣可以包括含铬土壤或含铬废物。
将各层铺设完成后,不定期从堆场上部注碳源溶液,不定期将渗滤液通过底部导流材料5收集至渗滤液收集系统中,随后将渗滤液回流至堆场顶部进行喷洒回灌。碳源溶液包括含有乙醇、甲醇、乙酸中一种或多种的溶液,其既可以作为微生物碳源, 也可以用于萃取飞灰中的二噁英等持久性有机污染物。碳源溶液可选地掺杂有硫酸亚铁,并且碳源溶液中碳源质量百分含量不高于50%。
进一步的,渗滤液回流至堆场顶部进行喷洒回灌的喷洒间隔时间为1-48小时。将渗滤液回流至堆场顶部进行喷洒回灌时对渗滤液可以对进行pH调节,使回灌的渗滤液pH值为2-5,pH值的调节可以通过加酸装置1来实现。在这样的pH值下,微电解陶粒会释放一定量的铁离子,在电催化所产生的微量羟基自由基作用下,产生芬顿催化效应,有效地降解二噁英污染,同时过程中将沼渣所产生的难降解有机物去除。可选的,运行期间,在堆场上部注碳源溶液的频率为每1-100天一次。
本申请实施例的具有以下特点:
1.硫酸亚铁将铬渣无害化同时,释放铁跟硫酸盐,铁可以作为芬顿效应的原料,硫酸盐作为沼渣中硫酸盐还原菌的原料进一步参与下一步生化反应。
2.通过内电解陶粒,形成电催化效应,产生羟基自由基,伴随pH的调整(pH在2-5)及Fe-C型内电解陶粒中Fe的释放,会产生芬顿高级氧化效应,可对飞灰中二噁英进行脱Cl反应,使二噁英转变为危害较低的有机物,同时协同沼渣中微生物代谢并处理二噁英污染,形成高级氧化及生化协同处置二噁英污染的效应。
3.利用沼渣处置飞灰,以废治废,即处置了飞灰,也将沼渣污染无害化。
4.沼渣中硫酸盐还原菌充分利用硫酸亚铁固定化重金属,相比直接使用化学固化剂固定重金属,具有生态安全的特点。
5.磷源、氮源及微量元素的加入进一步促进了沼渣中微生物的活性,增强了其处置持久性有机污染物(Persistent Organic Pollutants,简称POPs)的能力。
6.渗滤液中包含着沼渣的溶出液,其中含有大量诸如微生物残体在内的大分子有机质,难以被生物利用,即可生化性不强,通过回流至混合填埋场顶部,在内电解陶粒的作用下,大分子转变成小分子,提高了可生化性,随后这部分渗滤液进入混合层,会更好的被沼渣中微生物获取利用,从整体上加快了沼渣的生物降解。
7.飞灰中含有大量的Cl,进入渗滤液后,通过内电解作用,将渗滤液中Cl离子转变为Cl
2离开填埋场,从而降低填埋场中氯含量。同时Cl
2的产生也会对填埋场有害微生物进行消毒处理。
8.在内电解陶粒上所加的酸,既可以作为内电解陶粒运行的重要原料,也可以所谓中和铬渣及飞灰等高碱性危险废物的原料,使得填埋场趋向于中性。
以下结合实施例对本申请的特征和性能作进一步的详细描述。
实施例1
本实施例提供了一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,该方法包括将飞 灰及铬渣转移到堆场中;堆场内铺设防渗层3,底部铺设导流材料5,其上部铺设沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层4,碳源选为餐厨垃圾。按质量计,飞灰、铬渣、沼渣、餐厨垃圾、硫酸亚铁及营养添加剂的添加比例为1:0.5:0.2:0.2:0.15:0.1,混合层4的厚度为5m,混合层4上部放置内电解陶粒,厚度为0.1m;运行过程中,每隔1-5天从堆场上部注碳源溶液,本实施例中碳源溶液为乙醇溶液。随后将渗滤液通过底部导流材料5收集至渗滤液收集系统中,随后每间隔1天将渗滤液回流至堆场上部进行回灌,回流前调节pH至4。
经过60天处置,堆场中固体六价铬含量从3000mg/kg降低至不足2mg/kg,堆场中固体废物中重金属溶出率降低91%,Pb从5mg/L降低至不足0.1mg/L,Cd从3mg/L降低至不足0.1mg/L,同时二噁英等污染物去除率超过99%,二噁英含量达标。本实例的营养添加剂是磷酸钾、硝酸铵及硝酸钴的混合物,同时添加了微量的锌元素,内电解陶粒为Fe-C型内电解陶粒。
实施例2
本实施例提供了一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,该方法包括将飞灰及铬渣转移到堆场中;堆场内铺设防渗层3,底部铺设导流材料5,其上部铺设沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层4,碳源选为餐厨垃圾。按质量计,飞灰、铬渣、沼渣、餐厨垃圾、硫酸亚铁及营养添加剂的添加比例为1:2:0.5:0.4:0.3:0.1,混合层4的厚度为5m,混合层4上部放置内电解陶粒,厚度为0.01m;运行过程中,每隔30天从堆场上部注乙醇溶液,随后将渗滤液通过底部导流材料5收集至渗滤液收集系统中,随后每间隔2天将渗滤液回流至堆场上部进行回灌,回流前调节pH至4。
经过60天处置,堆场中固体六价铬含量从3000mg/kg降低至不足2mg/kg,堆场中固体废物中重金属溶出率降低91%,Pb从5mg/L降低至不足0.1mg/L,Cd从3mg/L降低至不足0.1mg/L,同时二噁英等污染物从500ng/kg降低至8ng/kg,去除率超过99%,二噁英含量达标。渗滤液COD从超过10000mg/L降低至不足200mg/L。本实例的营养添加剂是磷酸钾、硝酸铵及硝酸钴的混合物,同时添加了微量的锌元素,内电解陶粒为Fe-C型内电解陶粒。
实施例3
本实施例提供了一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,该方法包括将飞灰及铬渣转移到堆场中;堆场内铺设防渗层3,底部铺设导流材料5,其上部铺设沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层4,碳源选为餐厨垃圾。按质量计,飞灰、铬渣、沼渣、餐厨垃圾、硫酸亚铁及营养添加剂的添加比例为1:1.5:0.5:0.4:0.2:0.1,混合层4的厚度为5m,混合层4上部不设置内电解陶粒层2;运行过程中,每隔25天从堆场上部注乙醇溶液,随后将渗滤液通过底部导流材料5收集至渗滤液收集系统中, 随后每间隔2天将渗滤液回流至堆场上部进行回灌,回流前调节pH至4。
经过70天处置,堆场中固体六价铬含量从3000mg/kg降低至不足2mg/kg,堆场中固体废物中重金属溶出率降低91%,Pb从5mg/L降低至不足0.1mg/L,Cd从3mg/L降低至不足0.1mg/L,同时二噁英等污染物去除率超过99%,二噁英含量达标。渗滤液COD从超过10000mg/L降低至不足500mg/L。本实例的营养添加剂是磷酸钾、硝酸铵及硝酸钴的混合物,同时添加了微量的锌元素。
实施例4
将飞灰及铬渣转移到堆场中;堆场内铺设防渗层3,底部铺设导流材料5,其上部铺设污泥、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层4,碳源选为餐厨垃圾。按质量计,飞灰、铬渣、沼渣、餐厨垃圾、硫酸亚铁及营养添加剂的添加比例为1:2:0.5:0.4:0.3:0.1,混合层4的厚度为5m,混合层4上部放置内电解陶粒,厚度为0.01m;运行过程中,每隔30天从堆场上部注乙醇溶液及硫酸亚铁的混合液,随后将渗滤液通过底部导流材料5收集至渗滤液收集系统中,随后每间隔2天将渗滤液回流至堆场上部进行回灌,回流前调节pH至4。
经过70天处置,堆场中固体六价铬含量从3000mg/kg降低至不足2mg/kg,堆场中固体废物中重金属溶出率降低91%,Pb从5mg/L降低至不足0.1mg/L,Cd从3mg/L降低至不足0.1mg/L,同时二噁英等污染物去除率超过99%,二噁英含量达标。渗滤液COD从超过10000mg/L降低至不足300mg/L。本实例的营养添加剂是磷酸钾、硝酸铵及硝酸钴的混合物,同时添加了微量的锌元素。
实施例5
本实施例提供了一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,该方法包括将飞灰及铬渣转移到堆场中;堆场内铺设防渗层3,底部铺设导流材料5,其上部铺设沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层4,碳源选为餐厨垃圾。按质量计,飞灰、铬渣、沼渣、餐厨垃圾、硫酸亚铁及营养添加剂的添加比例为1:6:2:2:1.5:0.5,混合层4的厚度为5m,混合层4上部放置内电解陶粒,厚度为0.1m;运行过程中,每隔70天从堆场上部注碳源溶液,本实施例中碳源溶液为甲醇溶液。随后将渗滤液通过底部导流材料5收集至渗滤液收集系统中,随后每间隔1小时将渗滤液回流至堆场上部进行回灌,回流前调节pH至2。
经过80天处置,堆场中固体六价铬含量从3000mg/kg降低至不足2mg/kg,堆场中固体废物中重金属溶出率降低91%,Pb从5mg/L降低至不足0.1mg/L,Cd从3mg/L降低至不足0.1mg/L,同时二噁英等污染物去除率超过99%,二噁英含量达标。渗滤液COD从超过10000mg/L降低至不足100mg/L。本实例的营养添加剂是磷酸钾、硝酸铵及硝酸钴的混合物, 同时添加了微量的锌元素。
实施例6
本实施例提供了一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,该方法包括将飞灰及铬渣转移到堆场中;堆场内铺设防渗层3,底部铺设导流材料5,其上部铺设沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层4,碳源选为餐厨垃圾。按质量计,飞灰、铬渣、沼渣、餐厨垃圾、硫酸亚铁及营养添加剂的添加比例为1:3.5:2:2.5:2:0.5,混合层4的厚度为1m,混合层4上部放置内电解陶粒,厚度为0.6m;运行过程中,每隔100天从堆场上部注碳源溶液,本实施例中碳源溶液为乙酸溶液。随后将渗滤液通过底部导流材料5收集至渗滤液收集系统中,随后每间隔2天将渗滤液回流至堆场上部进行回灌,回流前调节pH至5。
经过120天处置,堆场中固体六价铬含量从3000mg/kg降低至不足2mg/kg,堆场中固体废物中重金属溶出率降低91%,Pb从5mg/L降低至不足0.1mg/L,Cd从3mg/L降低至不足0.1mg/L,同时二噁英等污染物去除率超过99%,二噁英含量达标。本实例的营养添加剂是磷酸钾、硝酸铵及硝酸钴的混合物,同时添加了微量的锌元素。
实施例7
本实施例提供了一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,该方法包括将飞灰及铬渣转移到堆场中;堆场内铺设防渗层3,底部铺设导流材料5,其上部铺设沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层4,碳源选为餐厨垃圾。按质量计,飞灰、铬渣、沼渣、餐厨垃圾、硫酸亚铁及营养添加剂的添加比例为1:10:5:5:3:1,混合层4的厚度为8m,混合层4上部放置内电解陶粒,厚度为1m;运行过程中,每隔30天从堆场上部注碳源溶液,本实施例中碳源溶液为甲醇溶液和硫酸亚铁的混合液。随后将渗滤液通过底部导流材料5收集至渗滤液收集系统中,随后每间隔1天将渗滤液回流至堆场上部进行回灌,回流前调节pH至4。
经过60天处置,堆场中固体六价铬含量从3000mg/kg降低至不足2mg/kg,堆场中固体废物中重金属溶出率降低91%,Pb从5mg/L降低至不足0.1mg/L,Cd从3mg/L降低至不足0.1mg/L,同时二噁英等污染物去除率超过99%,二噁英含量达标。渗滤液COD从超过10000mg/L降低至不足200mg/L。本实例的营养添加剂是磷酸钾、硝酸铵及硝酸钴的混合物,同时添加了微量的锌元素。
以上实施方式显示和描述了本申请的基本原理和主要特征和本申请的优点。本行业的技术人员应该了解,本申请不受上述实施例的限制,上述实施例和说明书中描述的只是说明本申请的原理,在不脱离本申请精神和范围的前提下,本申请还会有各种变化和改进,这些变化和改进都落入要求保护的本申请范围内。本申请要求保护范围由所附的权利要求 书及其等效物界定。
本申请的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法可以利用碳源溶液将飞灰中的二噁英萃取进溶液中,在内电解陶粒的作用下,促进二噁英的分解。并使重金属与硫化物反应生成极低溶解度的沉淀物,将铬渣无害化。通过该方法能够改善垃圾焚烧飞灰以及铬渣对环境的负面影响,并快速降解沼渣等有机废物中有机质含量,促进其快速稳定化。
Claims (16)
- 一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,包括:在用于飞灰及铬渣处置的堆场内铺设防渗层,底部铺设导流材料,其上部铺设包括沼渣、碳源、硫酸亚铁、营养添加剂、飞灰及铬渣的混合层,所述混合层上部放置内电解陶粒层;运行过程中,不定期从堆场上部注碳源溶液,不定期将渗滤液通过底部导流材料收集至渗滤液收集系统中,随后将所述渗滤液回流至所述堆场顶部进行喷洒回灌。
- 根据权利要求1所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述混合层中的所述飞灰、所述铬渣、所述沼渣、所述碳源、所述硫酸亚铁及所述营养添加剂按质量计添加比例为1:(0.1-10):(0.01-5):(0.01-5):(0.15-3):(0.1-1)。
- 根据权利要求1或2所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述混合层的厚度为1-8m;所述内电解陶粒层的厚度不超过1m。
- 根据权利要求1-3中任一项所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述渗滤液回流至所述堆场顶部进行喷洒回灌的喷洒间隔时间为1-48小时。
- 根据权利要求1-4中任一项所述种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,将所述渗滤液回流至所述堆场顶部进行喷洒回灌时对所述渗滤液进行pH调节,使回灌的所述渗滤液pH值为2-5。
- 根据权利要求1-5中任一项所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,沼渣包括有机废水、固体有机废物或污泥。
- 根据权利要求6所述的一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述沼渣为经厌氧处理后的固体有机废物。
- 根据权利要求1-7中任一项所述种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,运行期间,在所述堆场上部注所述碳源溶液的频率为每1-100天一次。
- 根据权利要求1-8中任一项所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述营养添加剂包括氮源、磷源及微量元素源中的一种或多种。
- 根据权利要求9所述的一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述碳源溶液中碳源质量百分含量不高于50%。
- 根据权利要求9所述的一种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述微量元素源包括含有硼、锌、铜、锰、钴中的一种或多种元素的营养 物质。
- 根据权利要求1-11中任一项所述种填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述碳源溶液包括含有乙醇、甲醇、乙酸中一种或多种的溶液。
- 根据权利要求1-12中任一项所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述碳源溶液掺杂有硫酸亚铁。
- 根据权利要求1-13中任一项所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述飞灰包括经过生化、物理或化学处置后的飞灰。
- 根据权利要求1-14中任一项所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述铬渣包括含铬土壤或含铬废物。
- 根据权利要求1-15中任一项所述的填埋场内协同处置垃圾焚烧飞灰及铬渣的方法,其特征在于,所述内电解陶粒层的内电解陶粒为Fe-C型内电解陶粒,所述内电解陶粒中含有金属铁及碳材料。
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CN114130785B (zh) * | 2021-11-09 | 2022-12-27 | 深圳能源环保股份有限公司 | 一种垃圾焚烧炉的飞灰处理方法 |
CN114669587B (zh) * | 2022-03-28 | 2023-04-07 | 中国环境科学研究院 | 生活垃圾协同处置膜浓缩液淋滤飞灰的方法、得到的残渣及应用 |
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