WO2019218420A1 - 一种有机废弃物快速转化能源的方法 - Google Patents
一种有机废弃物快速转化能源的方法 Download PDFInfo
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- WO2019218420A1 WO2019218420A1 PCT/CN2018/092030 CN2018092030W WO2019218420A1 WO 2019218420 A1 WO2019218420 A1 WO 2019218420A1 CN 2018092030 W CN2018092030 W CN 2018092030W WO 2019218420 A1 WO2019218420 A1 WO 2019218420A1
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- 238000000034 method Methods 0.000 title claims abstract description 32
- 239000010815 organic waste Substances 0.000 title claims abstract description 29
- 230000009466 transformation Effects 0.000 title abstract 3
- 238000000855 fermentation Methods 0.000 claims abstract description 43
- 230000004151 fermentation Effects 0.000 claims abstract description 36
- 239000007788 liquid Substances 0.000 claims abstract description 34
- 239000000446 fuel Substances 0.000 claims abstract description 29
- 239000007791 liquid phase Substances 0.000 claims abstract description 28
- 230000003197 catalytic effect Effects 0.000 claims abstract description 15
- 238000000926 separation method Methods 0.000 claims abstract description 10
- 239000007790 solid phase Substances 0.000 claims abstract description 8
- 239000005416 organic matter Substances 0.000 claims description 25
- DHRLEVQXOMLTIM-UHFFFAOYSA-N phosphoric acid;trioxomolybdenum Chemical compound O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.OP(O)(O)=O DHRLEVQXOMLTIM-UHFFFAOYSA-N 0.000 claims description 18
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 6
- 238000005119 centrifugation Methods 0.000 claims description 6
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 6
- 238000001914 filtration Methods 0.000 claims description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 6
- 238000011084 recovery Methods 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 3
- YVBOZGOAVJZITM-UHFFFAOYSA-P ammonium phosphomolybdate Chemical compound [NH4+].[NH4+].[NH4+].[NH4+].[O-]P([O-])=O.[O-][Mo]([O-])(=O)=O YVBOZGOAVJZITM-UHFFFAOYSA-P 0.000 claims description 3
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- 239000004310 lactic acid Substances 0.000 claims description 3
- 235000014655 lactic acid Nutrition 0.000 claims description 3
- 239000006249 magnetic particle Substances 0.000 claims description 3
- 239000012528 membrane Substances 0.000 claims description 3
- 239000004005 microsphere Substances 0.000 claims description 3
- 239000007800 oxidant agent Substances 0.000 claims description 3
- 235000019260 propionic acid Nutrition 0.000 claims description 3
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 3
- 150000003384 small molecules Chemical class 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 239000002244 precipitate Substances 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims 1
- 239000003792 electrolyte Substances 0.000 claims 1
- 239000012530 fluid Substances 0.000 claims 1
- AMWVZPDSWLOFKA-UHFFFAOYSA-N phosphanylidynemolybdenum Chemical compound [Mo]#P AMWVZPDSWLOFKA-UHFFFAOYSA-N 0.000 claims 1
- 239000011368 organic material Substances 0.000 abstract 3
- 238000004064 recycling Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000005516 engineering process Methods 0.000 description 5
- 239000010806 kitchen waste Substances 0.000 description 4
- 150000002632 lipids Chemical class 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 238000010170 biological method Methods 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000010344 co-firing Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000010336 energy treatment Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000023266 generation of precursor metabolites and energy Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 150000004666 short chain fatty acids Chemical class 0.000 description 1
- 235000021391 short chain fatty acids Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/52—Propionic acid; Butyric acids
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/28—Anaerobic digestion processes
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F11/00—Treatment of sludge; Devices therefor
- C02F11/02—Biological treatment
- C02F11/04—Anaerobic treatment; Production of methane by such processes
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F11/00—Treatment of sludge; Devices therefor
- C02F11/12—Treatment of sludge; Devices therefor by de-watering, drying or thickening
- C02F11/121—Treatment of sludge; Devices therefor by de-watering, drying or thickening by mechanical de-watering
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/005—Combined electrochemical biological processes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/06—Ethanol, i.e. non-beverage
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/56—Lactic acid
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
- H01M8/0606—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
- H01M8/0612—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/18—Regenerative fuel cells, e.g. redox flow batteries or secondary fuel cells
- H01M8/184—Regeneration by electrochemical means
- H01M8/188—Regeneration by electrochemical means by recharging of redox couples containing fluids; Redox flow type batteries
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F11/00—Treatment of sludge; Devices therefor
- C02F11/12—Treatment of sludge; Devices therefor by de-watering, drying or thickening
- C02F11/121—Treatment of sludge; Devices therefor by de-watering, drying or thickening by mechanical de-watering
- C02F11/122—Treatment of sludge; Devices therefor by de-watering, drying or thickening by mechanical de-watering using filter presses
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F11/00—Treatment of sludge; Devices therefor
- C02F11/12—Treatment of sludge; Devices therefor by de-watering, drying or thickening
- C02F11/121—Treatment of sludge; Devices therefor by de-watering, drying or thickening by mechanical de-watering
- C02F11/127—Treatment of sludge; Devices therefor by de-watering, drying or thickening by mechanical de-watering by centrifugation
-
- 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
- C02F1/46109—Electrodes
- C02F2001/46133—Electrodes characterised by the material
- C02F2001/46138—Electrodes comprising a substrate and a coating
- C02F2001/46142—Catalytic coating
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/46115—Electrolytic cell with membranes or diaphragms
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2303/00—Specific treatment goals
- C02F2303/10—Energy recovery
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2303/00—Specific treatment goals
- C02F2303/18—Removal of treatment agents after treatment
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- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
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- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
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- 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/20—Sludge processing
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- 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/30—Wastewater or sewage treatment systems using renewable energies
Definitions
- the invention relates to the technical field of organic waste energy, in particular to a method for rapidly converting energy of organic waste.
- Organic waste includes organic wastewater, sludge, kitchen waste, etc. These wastes contain a lot of water, but they also contain high organic matter content and have the potential to convert energy.
- the main ways to energyize organic waste include thermochemical methods and biological methods. Thermochemical methods include incineration, co-firing, pyrolysis and the like. These technologies require pre-dehydration and drying of organic waste, which consumes a large amount of energy, and the energy recovery efficiency of the combustion process is low.
- the biological method mainly converts organic waste into methane and other combustible gas through anaerobic microorganisms.
- fuel cells are a new type of organic energy conversion energy pathway with high energy efficiency.
- a liquid catalytic fuel cell can utilize a complex organic matter containing a large amount of water as a fuel under low temperature conditions ( ⁇ 100 ° C).
- the existing liquid-flow catalytic fuel cell cannot convert lipids, and the catalyst cannot be separated from the treatment residue, so it cannot be practically used for treating organic waste.
- the present invention proposes a method for rapidly converting energy into organic waste, which can significantly improve the efficiency of converting organic waste into energy.
- a method for rapidly converting energy from organic waste includes the following steps:
- the solid phase portion is disposed or reused as a residue, and the liquid phase portion enters the liquid flow to catalyze the fuel cell to convert the organic matter in the liquid phase portion into electrical energy.
- the above technical solution provided by the invention combines anaerobic fermentation technology and improved liquid flow catalytic fuel cell technology, wherein anaerobic fermentation technology can realize rapid conversion and decomposition of complex organic waste containing lipid components, and liquid catalytic fuel Battery technology can quickly and directly convert fermentation broth into electrical energy, thereby increasing the efficiency of converting organic waste into electrical energy.
- the treatment cycle of the method of the present invention can be shortened to 3 to 7 days, and the energy efficiency can be improved, compared with the treatment cycle of anaerobic digestion for 15 to 30 days and the energy conversion rate of only 15 to 40%. To 45 to 50%.
- the liquid catalytic fuel cell uses a proton exchange membrane to separate the anode and the cathode, the anolyte uses phosphomolybdic acid as a catalyst, and air or pure oxygen as a cathode oxidant; when the liquid phase partially enters the liquid stream After catalyzing the fuel cell, the flow-catalyzed fuel cell is operated at 80 to 95 ° C to convert the organic matter in the liquid phase portion into electrical energy.
- the phosphomolybdic acid is dissolved in an anolyte of the flow catalytic fuel cell. More preferably, after the process of converting the organic matter in the liquid phase portion into electrical energy is completed, an ammonium salt is added to the anolyte to form an ammonium phosphomolybdate precipitate for recovery of phosphomolybdic acid.
- the phosphomolybdic acid is attached to the anode electrode of the liquid flow catalytic fuel cell, and after the process of converting the organic matter in the liquid phase portion into electrical energy is completed, the residual moisture directly flows out of the liquid flow catalysis The fuel cell.
- the phosphomolybdic acid is combined with the insoluble particles, and after the process of converting the organic matter in the liquid phase portion into electrical energy, the phosphomolybdic acid is recovered by filtration, centrifugation or magnetic field separation;
- the insoluble particles include carbon microspheres and/or magnetic particles.
- step S1 is carried out in a fermentation reactor. More preferably, the fermentation reactor employs butyric acid fermentation, propionic acid fermentation, ethanol fermentation, lactic acid fermentation or alkaline fermentation.
- step S2 when the solid-liquid separation is carried out in step S2, a filtration method or a centrifugation method is employed.
- a specific embodiment of the present invention provides a method for rapidly converting energy from organic waste, comprising the following steps S1, S2 and S3:
- Step S1 performing anaerobic fermentation on the organic waste to convert the macromolecular organic matter in the organic waste into a soluble small molecule organic matter to obtain a fermentation liquid; the anaerobic fermentation may be performed in a fermentation reactor
- the fermentation type may be a butyric acid fermentation, a propionic acid fermentation, an ethanol fermentation, a lactic acid fermentation or an alkaline fermentation, and the like, and the like.
- the organic waste is an organic waste containing lipids, and after the anaerobic fermentation, the lipid component is decomposed into small-chain fatty acids such as short-chain fatty acids and glycerin.
- Step S2 performing solid-liquid separation on the fermentation liquid to obtain a solid phase portion and a liquid phase portion, respectively, and the solid-liquid separation in this step may be carried out by filtration or centrifugation.
- Step S3 the solid phase portion is disposed or reused as a residue, and the liquid phase portion enters the liquid stream to catalyze the fuel cell to convert the organic matter in the liquid phase portion into electrical energy.
- the liquid catalytic fuel cell used in the present invention uses a proton exchange membrane to separate the anode and the cathode, the anolyte uses phosphomolybdic acid H 3 PMo 12 O 40 as a catalyst, and the cathode uses air or pure oxygen as a catalyst. Oxidizer.
- the battery is operated at 80 to 95 ° C to directly convert the organic matter in the liquid phase portion of the fermentation liquid into electrical energy.
- the phosphomolybdic acid as the anode catalyst may be dissolved in the anolyte of the fuel cell, or may be insoluble or adhered to the anode electrode or may be combined with insoluble particles such as carbon microspheres and/or magnetic particles.
- an ammonium salt may be added to the anolyte. Recovery of phosphomolybdic acid is carried out by precipitation of ammonium phosphomolybdate.
- the phosphomolybdic acid is attached to the anode electrode, after the process of converting the organic matter in the liquid phase portion into electrical energy, the remaining moisture directly flows out of the liquid catalytic fuel cell; in the phosphomolybdic acid
- the recovery of the phosphomolybdic acid is carried out by a filtration method, a centrifugation method or a magnetic field separation method after the completion of the conversion of the organic matter in the liquid phase portion into electric energy.
- the method of the present invention is used for rapid energy treatment.
- the kitchen waste is placed in a fermentation reactor, and the residence time is set to 4 days, and the fermentation type is adjusted by butyric acid fermentation;
- the obtained fermentation broth is discharged from the fermentation reactor, and then centrifuged, and the organic carbon (TOC) in the supernatant (liquid phase portion) accounts for 80% of the total TOC of the kitchen waste; the supernatant enters the liquid flow catalysis.
- the initial TOC was 4.20 g/L after adjusting the concentration, and after treatment for 24 h, it was reduced to 1.30 g/L, and the conversion rate was about 70%.
- the entire process took 5 days, the organic matter conversion rate was 56% (in terms of TOC), and the system energy efficiency (output power/input energy) was 45.72%.
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Abstract
一种有机废弃物快速转化能源的方法,包括以下步骤:S1、对有机废弃物进行厌氧发酵,已使有机废弃物中的大分子有机质转化为可溶的小分子有机质,得到发酵液;S2、对发酵液进行固液分离,分别获得固相部分和液相部分;S3、所述固相部分作为残渣进行处置或再利用,所述液相部分进入液流催化燃料电池以使所述液相部分中的有机质转化为电能。该有机废弃物快速转化能源的方法能快速、高速地将有机废弃物转化为电能。
Description
本发明涉及有机废弃物能源化技术领域,尤其是涉及一种有机废弃物快速转化能源的方法。
有机废弃物包括有机废水、污泥、餐厨垃圾等,这些废弃物含有大量水分,但同时也含有较高的有机质含量,具有转化能源的潜力。目前有机废弃物能源化的主要途径包括热化学法和生物法等。热化学法包括焚烧、混烧、热解等技术,这些技术都需要对有机废弃物进行预先脱水、干燥,需要消耗大量能量,同时燃烧过程的能量回收效率较低。生物法主要是通过厌氧微生物将有机废弃物转化为甲烷等可燃气,但这一方法处理周期长,有机质转化率低,甲烷还需要进一步燃烧产热或产电,因此总体能量效率也较低。除上述方法外,燃料电池是一种新型的有机质转化能源途径,具有较高的能源效率。在多种燃料电池中,液流催化燃料电池可以在低温条件下(<100℃)利用含有大量水分的复杂有机质作为燃料。然而,现有的液流催化燃料电池不能转化脂类,催化剂也无法与处理残渣分离,因此还不能实际用于处理有机废弃物。
以上背景技术内容的公开仅用于辅助理解本发明的发明构思及技术方案,其并不必然属于本专利申请的现有技术,在没有明确的证据表明上述内容在本专利申请的申请日前已经公开的情况下,上述背景技术不应当用于评价本申请的新颖性和创造性。
发明内容
为弥补上述现有技术的不足,本发明提出一种有机废弃物快速转化能源的方法,能显著提高有机废弃物转化能源的效率。
本发明为达上述目的提出以下技术方案:
一种有机废弃物快速转化能源的方法,包括以下步骤:
S1、对有机废弃物进行厌氧发酵,以使所述有机废弃物中的大分子有机质转化为可溶的小分子有机质,得到发酵液;
S2、对所述发酵液进行固液分离,分别获得固相部分和液相部分;
S3、所述固相部分作为残渣进行处置或再利用,所述液相部分进入液流催化燃料电池以使所述液相部分中的有机质转化为电能。
本发明提供的上述技术方案,结合了厌氧发酵技术和改进的液流催化燃料电池技术,其中厌氧发酵技术可以实现含有脂类成分的复杂有机废弃物的快速转化和分解,液流催化燃料电池技术可以将发酵液快速、直接转化为电能,从而提高有机废弃物转化电能的效率。以有机废弃物污泥为例,相对于厌氧消化15~30天的处理周期和仅15~40%的能量转化率,本发明的方法处理周期可以缩短为3~7天,能量效率可以提高至45~50%。
优选地,所述液流催化燃料电池采用质子交换膜隔离阴阳两极,阳极电解液采用磷钼酸作为催化剂,以及,采用空气或纯氧作为阴极氧化剂;当所述液相部分进入所述液流催化燃料电池后,使所述液流催化燃料电池于80~95℃运行,以使所述液相部分中的有机质转化为电能。
优选地,所述磷钼酸溶解于所述液流催化燃料电池的阳极电解液中。更优选地,在完成所述液相部分中的有机质转化为电能的过程后,往所述阳极电解液中加入铵盐以形成磷钼酸铵沉淀进行磷钼酸的回收。
优选地,所述磷钼酸附着于所述液流催化燃料电池的阳极电极上,并且,在完成所述液相部分中的有机质转化为电能的过程后,剩余水分直接流出所述液流催化燃料电池。
优选地,所述磷钼酸与不溶性颗粒结合,并且,在完成所述液相部分中的有机质转化为电能的过程后,采用过滤法、离心法或磁场分离法回收所述磷钼酸;其中,所述不溶性颗粒包括碳微球和/或磁性颗粒。
优选地,步骤S1于一发酵反应器中进行。更优选地,所述发酵反应器采用丁酸发酵、丙酸发酵、乙醇发酵、乳酸发酵或碱性发酵。
优选地,步骤S2进行固液分离时,采用过滤法或离心法。
下面结合具体的实施方式对本发明作进一步说明。
本发明的具体实施方式提供了一种有机废弃物快速转化能源的方法,包括如下步骤S1、S2和S3:
步骤S1、对有机废弃物进行厌氧发酵,以使所述有机废弃物中的大分子有机质转化为可溶的小分子有机质,得到发酵液;所述厌氧发酵可在一发酵反应器中进行,发酵类型可以采用丁酸发酵、丙酸发酵、乙醇发酵、乳酸发酵或碱性发酵等等不限于此。在优选的实施例中,所述有机废弃物是含有脂类的有机废弃物,在进行厌氧发酵后,其中的脂类成分分解为短链脂肪酸和甘油等小分子有机质。
步骤S2、对所述发酵液进行固液分离,分别获得固相部分和液相部分,此步骤中进行所述固液分离可以采用过滤法或离心法。
步骤S3、所述固相部分作为残渣进行处置或再利用,所述液相部分进 入液流催化燃料电池以使所述液相部分中的有机质转化为电能。
在一种优选的实施例中,本发明所用的液流催化燃料电池采用质子交换膜隔离阴阳两极,阳极电解液采用磷钼酸H
3PMo
12O
40作为催化剂,阴极则采用空气或纯氧作为氧化剂。当所述液相部分进入该燃料电池后,使该电池于80~95℃运行,从而使发酵液中的液相部分中的有机质直接转化为电能。其中,作为阳极催化剂的所述磷钼酸可以溶解于该燃料电池的阳极电解液中,也可以不溶而是附着在阳极电极上或与碳微球和/或磁性颗粒等不溶性颗粒结合。
在磷钼酸溶解于所述液流催化燃料电池的阳极电解液的实施例中,当完成所述液相部分中的有机质转化为电能的过程后,可以往所述阳极电解液中加入铵盐以形成磷钼酸铵沉淀进行磷钼酸的回收。而在磷钼酸附着在所述阳极电极上的实施例中,在完成所述液相部分中的有机质转化为电能的过程后,剩余水分直接流出所述液流催化燃料电池;在磷钼酸与所述不溶性颗粒结合的实施例中,磷钼酸的回收是完成所述液相部分中的有机质转化为电能的过程后,采用过滤法、离心法或磁场分离法回收。
以某餐厨垃圾为例,采用本发明的前述方法进行快速能源化处理,首先将该餐厨垃圾置于发酵反应器,设置停留时间4天,通过碱液调控发酵类型为丁酸发酵;到时间则将得到的发酵液从发酵反应器排出,然后进行离心分离,上清液(液相部分)中有机碳(TOC)占该餐厨垃圾总TOC的80%;上清液进入液流催化燃料电池,调控浓度后初始TOC为4.20g/L,经24h处理后,降低至1.30g/L,转化率约70%。整个处理过程耗时5天,有机质转化率56%(以TOC计),系统能量效率(输出电能/输入能量)为45.72%。
以上内容是结合具体的优选实施方式对本发明所作的进一步详细说 明,不能认定本发明的具体实施只局限于这些说明。对于本发明所属技术领域的技术人员来说,在不脱离本发明构思的前提下,还可以做出若干等同替代或明显变型,而且性能或用途相同,都应当视为属于本发明的保护范围。
Claims (9)
- 一种有机废弃物快速转化能源的方法,包括以下步骤:S1、对有机废弃物进行厌氧发酵,以使所述有机废弃物中的大分子有机质转化为可溶的小分子有机质,得到发酵液;S2、对所述发酵液进行固液分离,分别获得固相部分和液相部分;S3、所述固相部分作为残渣进行处置或再利用,所述液相部分进入液流催化燃料电池以使所述液相部分中的有机质转化为电能。
- 如权利要求1所述的方法,其特征在于:所述液流催化燃料电池采用质子交换膜隔离阴阳两极,阳极电解液采用磷钼酸作为催化剂,以及,采用空气或纯氧作为阴极氧化剂;当所述液相部分进入所述液流催化燃料电池后,使所述液流催化燃料电池于80~95℃运行,以使所述液相部分中的有机质转化为电能。
- 如权利要求2所述的方法,其特征在于:所述磷钼酸溶解于所述液流催化燃料电池的阳极电解液中。
- 如权利要求3所述的方法,其特征在于:在完成所述液相部分中的有机质转化为电能的过程后,往所述阳极电解液中加入铵盐以形成磷钼酸铵沉淀进行磷钼酸的回收。
- 如权利要求2所述的方法,其特征在于:所述磷钼酸附着于所述液流催化燃料电池的阳极电极上,并且,在完成所述液相部分中的有机质转化为电能的过程后,剩余水分直接流出所述液流催化燃料电池。
- 如权利要求2所述的方法,其特征在于:所述磷钼酸与不溶性颗粒结合,并且,在完成所述液相部分中的有机质转化为电能的过程后,采用过滤法、离心法或磁场分离法回收所述磷钼酸;其中,所述不溶性颗粒包括碳微球和/或磁性颗粒。
- 如权利要求1至6任一项所述的方法,其特征在于:步骤S1于一发酵反应器中进行。
- 如权利要求7所述的方法,其特征在于:所述发酵反应器采用丁酸发酵、丙酸发酵、乙醇发酵、乳酸发酵或碱性发酵。
- 如权利要求1所述的方法,其特征在于:步骤S2进行固液分离时,采用过滤法或离心法。
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001229955A (ja) * | 2000-02-14 | 2001-08-24 | Toto Ltd | 発電システム |
US20040045885A1 (en) * | 2002-09-10 | 2004-03-11 | Sanyo Electric Co., Ltd. | Waste treatment system for treatment of organic waste and digested liquid thereof |
CN1868933A (zh) * | 2006-06-09 | 2006-11-29 | 浙江大学 | 生物质资源化循环利用的方法 |
CN101560524A (zh) * | 2009-05-21 | 2009-10-21 | 沈阳化工学院 | 一种利用生物燃料电池反应器产氢并发电转换的方法 |
CN102277388A (zh) * | 2011-06-20 | 2011-12-14 | 中国科学院广州能源研究所 | 一种有机废弃物联产氢气和电的方法及其装置 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001229955A (ja) * | 2000-02-14 | 2001-08-24 | Toto Ltd | 発電システム |
US20040045885A1 (en) * | 2002-09-10 | 2004-03-11 | Sanyo Electric Co., Ltd. | Waste treatment system for treatment of organic waste and digested liquid thereof |
CN1868933A (zh) * | 2006-06-09 | 2006-11-29 | 浙江大学 | 生物质资源化循环利用的方法 |
CN101560524A (zh) * | 2009-05-21 | 2009-10-21 | 沈阳化工学院 | 一种利用生物燃料电池反应器产氢并发电转换的方法 |
CN102277388A (zh) * | 2011-06-20 | 2011-12-14 | 中国科学院广州能源研究所 | 一种有机废弃物联产氢气和电的方法及其装置 |
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