US20130213280A9 - Methods and systems for reducing carbon dioxide emissions - Google Patents
Methods and systems for reducing carbon dioxide emissions Download PDFInfo
- Publication number
- US20130213280A9 US20130213280A9 US11/874,743 US87474307A US2013213280A9 US 20130213280 A9 US20130213280 A9 US 20130213280A9 US 87474307 A US87474307 A US 87474307A US 2013213280 A9 US2013213280 A9 US 2013213280A9
- Authority
- US
- United States
- Prior art keywords
- carbon dioxide
- lime
- zone
- limestone
- gaseous mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 title claims abstract description 199
- 239000001569 carbon dioxide Substances 0.000 title claims abstract description 98
- 229910002092 carbon dioxide Inorganic materials 0.000 title claims abstract description 98
- 238000000034 method Methods 0.000 title claims description 25
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims abstract description 61
- 235000011941 Tilia x europaea Nutrition 0.000 claims abstract description 61
- 239000004571 lime Substances 0.000 claims abstract description 61
- 238000002485 combustion reaction Methods 0.000 claims abstract description 54
- 235000019738 Limestone Nutrition 0.000 claims abstract description 44
- 239000006028 limestone Substances 0.000 claims abstract description 44
- 238000001354 calcination Methods 0.000 claims abstract description 38
- 239000000446 fuel Substances 0.000 claims abstract description 37
- 239000000463 material Substances 0.000 claims abstract description 26
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000001301 oxygen Substances 0.000 claims abstract description 22
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 22
- 239000007789 gas Substances 0.000 claims abstract description 15
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 230000036571 hydration Effects 0.000 claims abstract description 8
- 238000006703 hydration reaction Methods 0.000 claims abstract description 8
- 239000012528 membrane Substances 0.000 claims abstract description 6
- 230000004044 response Effects 0.000 claims abstract description 4
- 239000008246 gaseous mixture Substances 0.000 claims description 42
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 29
- 239000000920 calcium hydroxide Substances 0.000 claims description 29
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 29
- 235000011116 calcium hydroxide Nutrition 0.000 claims description 28
- 239000011575 calcium Substances 0.000 claims description 16
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 15
- 229910052791 calcium Inorganic materials 0.000 claims description 15
- 239000002594 sorbent Substances 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000000356 contaminant Substances 0.000 claims description 8
- 238000002309 gasification Methods 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 230000005611 electricity Effects 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 239000010881 fly ash Substances 0.000 claims description 4
- 230000000887 hydrating effect Effects 0.000 claims 2
- 230000008569 process Effects 0.000 description 11
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 10
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 10
- 238000010521 absorption reaction Methods 0.000 description 7
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- -1 tires Substances 0.000 description 5
- 230000007246 mechanism Effects 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 3
- 239000003245 coal Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000005201 scrubbing Methods 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 239000003344 environmental pollutant Substances 0.000 description 2
- 239000003546 flue gas Substances 0.000 description 2
- 239000010440 gypsum Substances 0.000 description 2
- 229910052602 gypsum Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 1
- 238000010744 Boudouard reaction Methods 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- PASHVRUKOFIRIK-UHFFFAOYSA-L calcium sulfate dihydrate Chemical compound O.O.[Ca+2].[O-]S([O-])(=O)=O PASHVRUKOFIRIK-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000012717 electrostatic precipitator Substances 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000005067 remediation Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J15/00—Arrangements of devices for treating smoke or fumes
- F23J15/006—Layout of treatment plant
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/22—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by diffusion
- B01D53/229—Integrated processes (Diffusion and at least one other process, e.g. adsorption, absorption)
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/62—Carbon oxides
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B7/00—Hydraulic cements
- C04B7/36—Manufacture of hydraulic cements in general
- C04B7/364—Avoiding environmental pollution during cement-manufacturing
- C04B7/367—Avoiding or minimising carbon dioxide emissions
-
- 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
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/02—Roasting processes
- C22B1/04—Blast roasting
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27B—FURNACES, KILNS, OVENS, OR RETORTS IN GENERAL; OPEN SINTERING OR LIKE APPARATUS
- F27B17/00—Furnaces of a kind not covered by any preceding group
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D17/00—Arrangements for using waste heat; Arrangements for using, or disposing of, waste gases
- F27D17/004—Systems for reclaiming waste heat
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/40—Alkaline earth metal or magnesium compounds
- B01D2251/404—Alkaline earth metal or magnesium compounds of calcium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/60—Inorganic bases or salts
- B01D2251/602—Oxides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/60—Inorganic bases or salts
- B01D2251/604—Hydroxides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/50—Carbon oxides
- B01D2257/504—Carbon dioxide
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2215/00—Preventing emissions
- F23J2215/50—Carbon dioxide
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2217/00—Intercepting solids
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2219/00—Treatment devices
- F23J2219/40—Sorption with wet devices, e.g. scrubbers
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2219/00—Treatment devices
- F23J2219/60—Sorption with dry devices, e.g. beds
-
- 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
- Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
- Y02C20/00—Capture or disposal of greenhouse gases
- Y02C20/40—Capture or disposal of greenhouse gases of CO2
-
- 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
- Y02E20/00—Combustion technologies with mitigation potential
- Y02E20/32—Direct CO2 mitigation
-
- 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
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/10—Production of cement, e.g. improving or optimising the production methods; Cement grinding
- Y02P40/18—Carbon capture and storage [CCS]
Definitions
- the reduced emission kiln includes the following: a combustion zone for generating a heat energy, the combustion zone including an oxygen inlet and a fuel inlet; and a calcination zone for converting limestone into lime and carbon dioxide in response to the heat energy from the combustion zone, the calcination zone including an inlet for limestone, a conduit for directing the carbon dioxide to the combustion zone for use as a flood gas to control the heat energy, an outlet for directing the lime to a hydration chamber, and a carbon dioxide permeable membrane for separating the carbon dioxide in the calcination zone from other materials in the calcination zone and preventing the other materials from entering the conduit for directing the carbon dioxide.
- a method of reducing emissions from a kiln includes the following: providing a carbonaceous fuel and oxygen; combusting the carbonaceous fuel and oxygen to form a gaseous mixture including carbon dioxide, the gaseous mixture providing a heat energy; providing limestone; mixing the gaseous mixture with the limestone thereby heating the limestone with the heat energy; converting the limestone to lime and carbon dioxide; separating carbon dioxide from the lime and from other materials in the gaseous mixture; and mixing at least a portion of the carbon dioxide separated from the lime and from other materials in the gaseous mixture with the carbonaceous fuel and oxygen while combusting the carbonaceous fuel and oxygen thereby controlling the heat energy.
- the reduced emission combustion system includes the following: a boiler including a combustion zone for combusting carbonaceous fuels to form a gaseous mixture, the gaseous mixture providing a heat energy; a particle separator for removing fly ash and other particulates from the gaseous mixture; a calcium-based heat exchanger configured to mix and heat steam and slaked lime to form lime and steam, configured to capture the exothermic heat of reaction when the lime reacts to form slaked lime, and configured to recycle the slaked lime to the beginning of the calcium-based heat exchange system, the calcium-based heat exchange system including means for collecting dissolved slaked lime; a dry or wet scrubber for removing contaminants present in the gaseous mixture, the dry or wet scrubber including means for utilizing the dissolved slaked lime from the calcium-based heat exchange system; a carbon dioxide removal chamber for removing carbon dioxide present in the gaseous mixture, the carbon dioxide removal chamber including a mechanism for bringing the gas
- FIG. 1 is a diagram of a reduced emission kiln according to some embodiments of the disclosed subject matter
- FIG. 2 is a diagram of a method of reducing emissions from a kiln according to some embodiments of the disclosed subject matter
- FIG. 3 is a diagram of a reduced emission combustion system according to some embodiments of the disclosed subject matter.
- FIG. 4 is a schematic cross-section of a heat exchanger according to some embodiments of the disclosed subject matter.
- reduced emission kiln 20 can include a kiln having total carbon dioxide emissions to the environment outside of the kiln of less than about 1% or 10,000 parts per million (ppm) of the total gas in the system. In some embodiments, the kiln releases from about 10,000 ppm to about 1 ppm of carbon dioxide into the environment outside of the kiln. In some embodiments, the kiln does not release any carbon dioxide into the environment outside of the kiln.
- reduced emission kiln 20 includes a combustion zone 22 and a calcination zone 24 .
- a carbonaceous fuel 26 is combusted in combustion zone 22 to heat calcination zone 24 .
- limestone 28 is heated until it converts to lime 30 and heated carbon dioxide (CO 2 ) 32 .
- limestone includes materials predominantly composed of calcium carbonate (CaCO 3 ), e.g., a material having CaCO 3 and MgCO 3 (dolomite) and the term “lime” as used herein refers to materials predominantly composed of calcium oxide (CaO), e.g., a material having CaO and MgO.
- carbonaceous fuel as used herein can include, but is not limited to, carbon, coal, fuel oil, natural gas, petro-coke, waste oil, a gaseous hydrocarbon, such as methane, ethane, propane or butane, tires, and biomass.
- Combustion zone 22 includes an oxygen inlet 34 and a fuel inlet 36 .
- a gas containing substantially oxygen or pure oxygen is fed to combustion zone 22 via oxygen inlet 34 to facilitate combustion of carbonaceous fuel 26 .
- Carbonaceous fuel 26 is introduced to combustion zone via fuel inlet 36 . Combustion of carbonaceous fuel 26 generates a heat energy 38 for heating calcination zone 24 .
- Calcination zone 24 includes an inlet 40 for limestone 28 , a conduit 42 for recycling carbon dioxide 32 to combustion zone 22 for use as a flood gas to temper the combustion reaction taking place in the kiln to control heat energy 38 , and an outlet 44 for directing lime 30 to a hydration chamber 46 .
- a hydration chamber 46 For example, use of high purity oxygen for combustion may excessively raise the temperature of the kiln and hot carbon dioxide 32 can be utilized as a flood gas to temper the flame temperature.
- lime 30 is hydrated to form slaked lime 48 .
- the term “slaked lime” as used herein refers to a material predominantly composed of calcium hydroxide Ca(OH) 2 .
- calcination zone 24 also includes a carbon dioxide permeable membrane 50 for separating carbon dioxide in the calcination zone from other materials in the calcination zone and preventing the other materials from entering conduit 42 .
- Carbon dioxide permeable membrane 50 is configured so that a substantially pure stream of carbon dioxide, i.e., carbon dioxide 32 , flows from calcination zone 24 into conduit 42 .
- a nearly complete combustion of carbon dioxide will take place in calcination zone 24 , thereby producing an effluent from the calcination zone of carbon dioxide and steam.
- the steam can be condensed and a concentrated stream of carbon dioxide produced and/or captured.
- reduced emission kiln 20 includes additional apparatus for capturing and sequestering portions of carbon dioxide 32 not used as a flood gas.
- calcination zone 24 can be a fluidized bed that avoids mixing air with the carbon dioxide produced in the calcination process.
- the calciner can be fluidized using a stream of gases, e.g., methane, carbon dioxide, etc., and the heat of combustion can be transferred to the reactive materials.
- the fluidized bed can operate at temperatures ranging from about room temperature to about 1000 degrees Celsius.
- the fluidized bed can produce a pure stream of carbon dioxide and a calcined product such as lime.
- reduced emission kiln 20 includes a preheating zone 52 for preheating limestone 28 before it enters calcination zone 24 .
- Preheating zone 52 includes a conduit 54 for directing preheated limestone 28 to calcination zone 24 .
- reduced emission kiln 20 includes a conduit 56 for directing heat energy 38 from combustion zone 22 to preheating zone 52 .
- an auxiliary heating source (not shown) is used to heat preheating zone 52 .
- reduced emission kiln 20 includes a gasification zone 58 to convert various non-gaseous fuels to a gas prior to burning.
- carbon dioxide 32 which is produced in calcination zone 24 , can be utilized to gasify carbonaceous fuel 26 , e.g., coal, in gasification zone 58 according to the Boudouard reaction prior to combusting in combustion zone 22 .
- an oxygen supply (not shown) and conduit (not shown) for providing oxygen to gasification zone 58 is included. Oxygen provided to gasification zone 58 can be utilized to gasify carbonaceous fuel 26 in the gasification zone prior to combusting in combustion zone 22 .
- some embodiments include a method 60 of reducing emissions from a kiln.
- carbonaceous fuel and oxygen are provided.
- the carbonaceous fuel and oxygen are combusted to form a heated gaseous mixture including carbon dioxide.
- the carbonaceous fuel is gasified prior to combusting.
- the heated gaseous mixture provides heat energy.
- limestone is provided.
- the heated gaseous mixture is mixed with the limestone thereby heating the limestone with the heat energy.
- the limestone is converted to lime and carbon dioxide.
- the limestone is preheated prior to converting.
- heat energy generated at 64 is used to preheat the limestone.
- the carbon dioxide is separated from the lime and from other materials in the gaseous mixture.
- the lime is hydrated to form slaked lime. Slaking the lime helps maintain its reactivity for future use as a carbon dioxide sorbent.
- a portion of the carbon dioxide separated from the lime and from other materials in the gaseous mixture is used as a flood gas to control the heat energy generated during combustion of the carbonaceous fuel and oxygen.
- a portion of the carbon dioxide separated from the lime and from other materials in the gaseous mixture is captured and sequestered.
- System 90 includes a boiler 92 , a particle separator 94 , a calcium-based heat exchanger 96 , a dry or wet scrubber 98 , a carbon dioxide removal chamber 100 , and a sorbent regenerator 102 .
- Boiler 92 includes a combustion zone 104 for combusting carbonaceous fuels 106 to form a heated gaseous mixture 108 .
- boiler 92 is operated at temperatures of at least about 1000 degrees.
- Gaseous mixture 108 provides a heat energy 110 to be used elsewhere in system 90 .
- solid ash can be created and removed from a point 112 adjacent the bottom of combustion zone 104 .
- Gaseous mixture 108 can contain carbon dioxide, fly ash, and other contaminants, e.g., sulfur dioxide (SO 2 ) gas.
- Particle separator 94 includes known mechanisms for removing fly ash and other particulates from a flue gas, i.e., from gaseous mixture 108 .
- particle separator 94 can be an electrostatic precipitator or filters.
- calcium-based heat exchanger 96 includes a heat absorption zone 114 , e.g., made of tubes, that contains a steam 116 and a slaked lime 118 .
- a heat source such as heat energy 110 is applied to heat absorption zone 114 to heat steam 116 and slaked lime 118 until it converts to a lime 120 and a steam 122 .
- the initial temperature of gaseous mixture 108 and resulting heat energy 110 can be above from 500 degrees Celsius to about 900 degrees Celsius. In some embodiments, the temperature of the heated lime 120 and or steam 122 can be above about 100 degrees Celsius to 900 degrees Celsius.
- heat absorption zone 114 can absorb up to about 100% of the heat from gaseous mixture 108 .
- Calcium-based heat exchanger 96 also includes a heat release zone 124 .
- lime 120 combines with steam 122 to re-form slaked lime 118
- the exothermic heat of reaction generated is captured by heat exchange tubes 126 or similar mechanisms in heat release zone 124 and used elsewhere in system 90 .
- Slaked lime 118 is recycled to heat absorption zone 114 .
- calcium-based heat exchanger 96 includes a mechanism (not shown), e.g., filter, drain, conduit, etc., for collecting any slaked lime that is dissolved in water in the heat exchanger.
- the dissolved slaked lime (not shown) can be used in dry or wet scrubber 98 to remove other contaminants from gaseous mixture 108 .
- calcium-based heat exchanger 96 can be integrally incorporated within combustion system 90 .
- gaseous mixture 108 can pass over heat absorption zone 114 and heat generated by the exothermic heat of reaction and captured by heat exchange tubes 126 can be utilized to dry solids entering combustion system 90 .
- the heat generated by the exothermic heat of reaction and captured by heat exchange tubes 126 can also be utilized to heat feed water and drive one or more turbines for generating electricity.
- heat absorption zone 114 , heat release zone 124 , and heat exchange tubes 126 are not necessarily limited as a component of combustion system 90 and can be embodied as a separate component that can be used in any suitable systems or processes.
- any heat containing substance can be contacted or passed over heat absorption zone 114 and the heat generated by the exothermic heat of reaction from the re-formation of slaked lime 118 can be utilized in any desired process, e.g., to heat feed water for another process.
- calcium-based heat exchanger 96 can be used to improve the efficiency of a Fischer-Tropsch process.
- Dry or wet scrubber 98 can be a conventional scrubber for removing other contaminants, e.g., sulfur dioxide, etc., present in gaseous mixture 108 .
- dry or wet scrubber 98 is connected with calcium-based heat exchanger 96 , which provides dissolved calcium hydroxide for use in the scrubber.
- dry sorbent scrubbing or lime spraying can be utilized in scrubber 98 .
- limestone pellets can be introduced to the top of a tank where the surface of the limestone pellets reacts with contaminants, e.g., sulfur dioxide, contained in gaseous mixture 108 .
- the reacted pellets can fall down into a hopper and then be fed into a device that scrapes the reacted outside layer of the limestone pellets.
- the regenerated limestone pellet can be fed back to the top of the tank and the scrubbing repeated.
- lime spraying powdered lime, either in a dry state or mixed with water to form a paste, can be used.
- the lime can be sprayed into gaseous mixture 108 inside a reaction chamber where it reacts with the contaminants. For example, if sulfur dioxide is the predominant contaminant to be removed, lime may turn into gypsum, which can be captured for use in other processes.
- gypsum refers to compounds including calcium sulfate dehydrate (CaSO 4 .2H 2 O).
- Carbon dioxide capture chamber 100 can be a conventional apparatus for removing carbon dioxide by bringing a mixture containing carbon dioxide, e.g., gaseous mixture 108 , into contact with lime or slaked lime to generate limestone.
- carbon dioxide capture chamber 100 can include a chamber, a tube, a container, or the like having holes that allow passage of carbon dioxide into and out of the chamber, tube, container, or the like.
- Carbon dioxide capture chamber 100 can also include a fluidized bed or circulating fluidized bed wherein lime or slaked lime are suspended on an upward blowing stream of carbon dioxide. In some embodiments, a bubbling fluidized bed can be utilized.
- Carbon dioxide capture chamber 100 can also include cyclones (not shown) that separate the solids and residual exhaust or flue gas before discharging any exhaust to the atmosphere via a stack 127 .
- the lime or slaked lime used in carbon dioxide capture chamber 100 can be generated in sorbent regenerator 102 .
- Sorbent regenerator 102 is used to generate lime and carbon dioxide from the limestone generated in carbon dioxide capture chamber 100 .
- sorbent regenerator 102 includes a conduit 128 for providing lime generated to carbon dioxide capture chamber 100 .
- sorbent regenerator 102 includes a conduit (not shown) for providing any excess lime generated to boiler 92 and combustion zone 104 for combustion.
- sorbent regenerator 102 is a low emission kiln such as reduced emission kiln 20 , which is described above.
- system 90 includes additional heat exchangers (not shown) for capturing heat generated in sorbent regenerator 102 .
- additional heat exchangers for capturing heat from calcination zone 24 and combustion zones 22 , 104 can be included.
- system 90 is used to heat steam and drive turbines to generate electricity.
- Heated gaseous mixture 108 can indirectly heat pipes 130 containing, for example, steam, which can then drive one or more turbines (not shown) to generate power, such as electricity.
- uses for an oxygen-blown reduced emission kiln according to the disclosed subject matter include, but are not limited to the following: the production of lime, clinker, and cement with reduced carbon dioxide emissions; reducing the emissions from power plants that run on coal or one or more fossil fuels; reducing carbon dioxide emissions from iron and steel blast furnaces; reducing emissions for paper production processes; for performing Fischer-Tropsch processes with reduced carbon dioxide emissions; and reducing carbon dioxide emissions in a system used for the heat treatment of solids or the volatilization of pollutants, such as a soil remediation method in which soil is burned to oxidize pollutants.
- an oxygen-blown reduced emission kiln according to the disclosed subject matter can be utilized to capture the carbon dioxide gases contained in the exhaust gas of one or more of the processes described above.
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Abstract
A reduced emission kiln is described. In some embodiments, the kiln includes a combustion zone for generating heat energy. The combustion zone includes an oxygen inlet and a fuel inlet. In some embodiments, the kiln also includes a calcination zone for converting limestone into lime and carbon dioxide in response to the heat energy from the combustion zone. The calcination zone includes an inlet for limestone, a conduit for directing the carbon dioxide to the combustion zone for use as a flood gas to control the heat energy, an outlet for directing the lime to a hydration chamber, and a carbon dioxide permeable membrane for separating the carbon dioxide in the calcination zone from other materials in the calcination zone and preventing the other materials from entering the conduit for directing the carbon dioxide.
Description
- This application claims the benefit of International Application Number PCT/US2006/014495, filed Apr. 18, 2006, which claims the benefit of U.S. Provisional Application No. 60/672,279, filed Apr. 18, 2005, each of which is incorporated by reference as if disclosed herein in its entirety.
- Climate change concerns have increased concerns over the level of carbon dioxide emissions from various processes. For example, the lime and cement industries are responsible for approximately 5% of global carbon dioxide emissions. Of these emissions, about 50% arise from the chemical liberation of carbon dioxide bound in carbonates and 40% from fuel consumption with the remainder associated with electricity use and transportation.
- Lime is manufactured from limestone and dolomite by heating these materials in a limekiln. This process results in the evolution of carbon dioxide. The predominant reaction in limekilns, which is commonly referred to as the calcination reaction, is shown in the following equation [1]:
-
CaCO3(s)→Ca(s)+CO2(g) [1] - Combustion of carbonaceous fuel is another process that generates carbon dioxide emissions. Currently, in one method used to reduce carbon dioxide emissions, lime is utilized to convert the carbon dioxide into limestone as shown in the following equation [2]:
-
CaO(s)+CO2(g)→CaCO3(s) [2] - Then, the limestone is fired and converted back into lime as shown Equation [1] and this cycle repeats. However, after repeated cycling, sintering of the lime occurs and its capacity to capture carbon dioxide is greatly reduced.
- A reduced emission kiln is disclosed. In some embodiments, the reduced emission kiln includes the following: a combustion zone for generating a heat energy, the combustion zone including an oxygen inlet and a fuel inlet; and a calcination zone for converting limestone into lime and carbon dioxide in response to the heat energy from the combustion zone, the calcination zone including an inlet for limestone, a conduit for directing the carbon dioxide to the combustion zone for use as a flood gas to control the heat energy, an outlet for directing the lime to a hydration chamber, and a carbon dioxide permeable membrane for separating the carbon dioxide in the calcination zone from other materials in the calcination zone and preventing the other materials from entering the conduit for directing the carbon dioxide.
- A method of reducing emissions from a kiln is disclosed. In some embodiments, the method includes the following: providing a carbonaceous fuel and oxygen; combusting the carbonaceous fuel and oxygen to form a gaseous mixture including carbon dioxide, the gaseous mixture providing a heat energy; providing limestone; mixing the gaseous mixture with the limestone thereby heating the limestone with the heat energy; converting the limestone to lime and carbon dioxide; separating carbon dioxide from the lime and from other materials in the gaseous mixture; and mixing at least a portion of the carbon dioxide separated from the lime and from other materials in the gaseous mixture with the carbonaceous fuel and oxygen while combusting the carbonaceous fuel and oxygen thereby controlling the heat energy.
- A reduced emission combustion system is disclosed. In some embodiments, the reduced emission combustion system includes the following: a boiler including a combustion zone for combusting carbonaceous fuels to form a gaseous mixture, the gaseous mixture providing a heat energy; a particle separator for removing fly ash and other particulates from the gaseous mixture; a calcium-based heat exchanger configured to mix and heat steam and slaked lime to form lime and steam, configured to capture the exothermic heat of reaction when the lime reacts to form slaked lime, and configured to recycle the slaked lime to the beginning of the calcium-based heat exchange system, the calcium-based heat exchange system including means for collecting dissolved slaked lime; a dry or wet scrubber for removing contaminants present in the gaseous mixture, the dry or wet scrubber including means for utilizing the dissolved slaked lime from the calcium-based heat exchange system; a carbon dioxide removal chamber for removing carbon dioxide present in the gaseous mixture, the carbon dioxide removal chamber including a mechanism for bringing the gaseous mixture into contact with lime or slaked lime to generate limestone; and a sorbent regenerator for generating lime and carbon dioxide from the limestone generated in the carbon dioxide removal chamber, the sorbent regenerator including means for providing the lime generated to the carbon dioxide removal chamber.
- The drawings show embodiments of the disclosed subject matter for the purpose of illustrating the invention. However, it should be understood that the present application is not limited to the precise arrangements and instrumentalities shown in the drawings, wherein:
-
FIG. 1 is a diagram of a reduced emission kiln according to some embodiments of the disclosed subject matter; -
FIG. 2 is a diagram of a method of reducing emissions from a kiln according to some embodiments of the disclosed subject matter; -
FIG. 3 is a diagram of a reduced emission combustion system according to some embodiments of the disclosed subject matter; and -
FIG. 4 is a schematic cross-section of a heat exchanger according to some embodiments of the disclosed subject matter. - Referring now to the drawings and in particular to
FIG. 1 , one aspect of the disclosed subject matter relates to a reducedemission kiln 20. The term “reduced emission kiln” as used herein can include a kiln having total carbon dioxide emissions to the environment outside of the kiln of less than about 1% or 10,000 parts per million (ppm) of the total gas in the system. In some embodiments, the kiln releases from about 10,000 ppm to about 1 ppm of carbon dioxide into the environment outside of the kiln. In some embodiments, the kiln does not release any carbon dioxide into the environment outside of the kiln. - In some embodiments, reduced
emission kiln 20 includes acombustion zone 22 and acalcination zone 24. Acarbonaceous fuel 26 is combusted incombustion zone 22 toheat calcination zone 24. Incalcination zone 24,limestone 28 is heated until it converts to lime 30 and heated carbon dioxide (CO2) 32. - As used herein, the term “limestone” includes materials predominantly composed of calcium carbonate (CaCO3), e.g., a material having CaCO3 and MgCO3 (dolomite) and the term “lime” as used herein refers to materials predominantly composed of calcium oxide (CaO), e.g., a material having CaO and MgO. The term “carbonaceous fuel” as used herein can include, but is not limited to, carbon, coal, fuel oil, natural gas, petro-coke, waste oil, a gaseous hydrocarbon, such as methane, ethane, propane or butane, tires, and biomass.
-
Combustion zone 22 includes anoxygen inlet 34 and afuel inlet 36. A gas containing substantially oxygen or pure oxygen is fed tocombustion zone 22 viaoxygen inlet 34 to facilitate combustion ofcarbonaceous fuel 26.Carbonaceous fuel 26 is introduced to combustion zone viafuel inlet 36. Combustion ofcarbonaceous fuel 26 generates aheat energy 38 forheating calcination zone 24. -
Calcination zone 24 includes aninlet 40 forlimestone 28, aconduit 42 forrecycling carbon dioxide 32 tocombustion zone 22 for use as a flood gas to temper the combustion reaction taking place in the kiln to controlheat energy 38, and anoutlet 44 for directing lime 30 to ahydration chamber 46. For example, use of high purity oxygen for combustion may excessively raise the temperature of the kiln andhot carbon dioxide 32 can be utilized as a flood gas to temper the flame temperature. Inhydration chamber 46, lime 30 is hydrated to formslaked lime 48. The term “slaked lime” as used herein refers to a material predominantly composed of calcium hydroxide Ca(OH)2. In some embodiments,calcination zone 24 also includes a carbon dioxidepermeable membrane 50 for separating carbon dioxide in the calcination zone from other materials in the calcination zone and preventing the other materials from enteringconduit 42. Carbon dioxidepermeable membrane 50 is configured so that a substantially pure stream of carbon dioxide, i.e.,carbon dioxide 32, flows fromcalcination zone 24 intoconduit 42. In some embodiments, a nearly complete combustion of carbon dioxide will take place incalcination zone 24, thereby producing an effluent from the calcination zone of carbon dioxide and steam. The steam can be condensed and a concentrated stream of carbon dioxide produced and/or captured. In some embodiments, reducedemission kiln 20 includes additional apparatus for capturing and sequestering portions ofcarbon dioxide 32 not used as a flood gas. - In some embodiments,
calcination zone 24 can be a fluidized bed that avoids mixing air with the carbon dioxide produced in the calcination process. The calciner can be fluidized using a stream of gases, e.g., methane, carbon dioxide, etc., and the heat of combustion can be transferred to the reactive materials. The fluidized bed can operate at temperatures ranging from about room temperature to about 1000 degrees Celsius. The fluidized bed can produce a pure stream of carbon dioxide and a calcined product such as lime. - In some embodiments, reduced
emission kiln 20 includes apreheating zone 52 for preheatinglimestone 28 before it enterscalcination zone 24. Preheatingzone 52 includes aconduit 54 for directing preheatedlimestone 28 tocalcination zone 24. In some embodiments, reducedemission kiln 20 includes aconduit 56 for directingheat energy 38 fromcombustion zone 22 to preheatingzone 52. In some embodiments, an auxiliary heating source (not shown) is used to heatpreheating zone 52. - In some embodiments, reduced
emission kiln 20 includes agasification zone 58 to convert various non-gaseous fuels to a gas prior to burning. For example,carbon dioxide 32, which is produced incalcination zone 24, can be utilized to gasifycarbonaceous fuel 26, e.g., coal, ingasification zone 58 according to the Boudouard reaction prior to combusting incombustion zone 22. In some embodiments, an oxygen supply (not shown) and conduit (not shown) for providing oxygen togasification zone 58 is included. Oxygen provided togasification zone 58 can be utilized to gasifycarbonaceous fuel 26 in the gasification zone prior to combusting incombustion zone 22. - Referring now to
FIG. 2 , some embodiments include amethod 60 of reducing emissions from a kiln. At 62, carbonaceous fuel and oxygen are provided. At 64, the carbonaceous fuel and oxygen are combusted to form a heated gaseous mixture including carbon dioxide. In some embodiments, the carbonaceous fuel is gasified prior to combusting. The heated gaseous mixture provides heat energy. At 66, limestone is provided. At 68, the heated gaseous mixture is mixed with the limestone thereby heating the limestone with the heat energy. At 70, the limestone is converted to lime and carbon dioxide. In some embodiments, the limestone is preheated prior to converting. In some embodiments, heat energy generated at 64 is used to preheat the limestone. At 72, the carbon dioxide is separated from the lime and from other materials in the gaseous mixture. At 74, the lime is hydrated to form slaked lime. Slaking the lime helps maintain its reactivity for future use as a carbon dioxide sorbent. At 76, a portion of the carbon dioxide separated from the lime and from other materials in the gaseous mixture is used as a flood gas to control the heat energy generated during combustion of the carbonaceous fuel and oxygen. At 78, a portion of the carbon dioxide separated from the lime and from other materials in the gaseous mixture is captured and sequestered. - Referring now to
FIGS. 3 and 4 , some embodiments include a reducedemission combustion system 90.System 90 includes aboiler 92, aparticle separator 94, a calcium-basedheat exchanger 96, a dry orwet scrubber 98, a carbondioxide removal chamber 100, and asorbent regenerator 102. -
Boiler 92 includes acombustion zone 104 for combustingcarbonaceous fuels 106 to form a heated gaseous mixture 108. In some embodiments,boiler 92 is operated at temperatures of at least about 1000 degrees. Gaseous mixture 108 provides a heat energy 110 to be used elsewhere insystem 90. Ascarbonaceous fuel 106 burns, solid ash can be created and removed from apoint 112 adjacent the bottom ofcombustion zone 104. Gaseous mixture 108 can contain carbon dioxide, fly ash, and other contaminants, e.g., sulfur dioxide (SO2) gas.Particle separator 94 includes known mechanisms for removing fly ash and other particulates from a flue gas, i.e., from gaseous mixture 108. For example,particle separator 94 can be an electrostatic precipitator or filters. - As best illustrated in
FIG. 4 , calcium-basedheat exchanger 96 includes aheat absorption zone 114, e.g., made of tubes, that contains a steam 116 and a slaked lime 118. A heat source such as heat energy 110 is applied toheat absorption zone 114 to heat steam 116 and slaked lime 118 until it converts to a lime 120 and a steam 122. The initial temperature of gaseous mixture 108 and resulting heat energy 110 can be above from 500 degrees Celsius to about 900 degrees Celsius. In some embodiments, the temperature of the heated lime 120 and or steam 122 can be above about 100 degrees Celsius to 900 degrees Celsius. In some embodiments,heat absorption zone 114 can absorb up to about 100% of the heat from gaseous mixture 108. Calcium-basedheat exchanger 96 also includes aheat release zone 124. When lime 120 combines with steam 122 to re-form slaked lime 118, the exothermic heat of reaction generated is captured byheat exchange tubes 126 or similar mechanisms inheat release zone 124 and used elsewhere insystem 90. Slaked lime 118 is recycled to heatabsorption zone 114. In some embodiments, calcium-basedheat exchanger 96 includes a mechanism (not shown), e.g., filter, drain, conduit, etc., for collecting any slaked lime that is dissolved in water in the heat exchanger. The dissolved slaked lime (not shown) can be used in dry orwet scrubber 98 to remove other contaminants from gaseous mixture 108. - In some embodiments, calcium-based
heat exchanger 96 can be integrally incorporated withincombustion system 90. For example, gaseous mixture 108 can pass overheat absorption zone 114 and heat generated by the exothermic heat of reaction and captured byheat exchange tubes 126 can be utilized to dry solids enteringcombustion system 90. As discussed further below, the heat generated by the exothermic heat of reaction and captured byheat exchange tubes 126 can also be utilized to heat feed water and drive one or more turbines for generating electricity. - In some embodiments,
heat absorption zone 114,heat release zone 124, andheat exchange tubes 126 are not necessarily limited as a component ofcombustion system 90 and can be embodied as a separate component that can be used in any suitable systems or processes. For example, any heat containing substance can be contacted or passed overheat absorption zone 114 and the heat generated by the exothermic heat of reaction from the re-formation of slaked lime 118 can be utilized in any desired process, e.g., to heat feed water for another process. For example, calcium-basedheat exchanger 96 can be used to improve the efficiency of a Fischer-Tropsch process. - Dry or
wet scrubber 98 can be a conventional scrubber for removing other contaminants, e.g., sulfur dioxide, etc., present in gaseous mixture 108. In some embodiments, dry orwet scrubber 98 is connected with calcium-basedheat exchanger 96, which provides dissolved calcium hydroxide for use in the scrubber. For example, dry sorbent scrubbing or lime spraying can be utilized inscrubber 98. - In dry sorbent scrubbing, limestone pellets can be introduced to the top of a tank where the surface of the limestone pellets reacts with contaminants, e.g., sulfur dioxide, contained in gaseous mixture 108. The reacted pellets can fall down into a hopper and then be fed into a device that scrapes the reacted outside layer of the limestone pellets. The regenerated limestone pellet can be fed back to the top of the tank and the scrubbing repeated.
- In lime spraying, powdered lime, either in a dry state or mixed with water to form a paste, can be used. The lime can be sprayed into gaseous mixture 108 inside a reaction chamber where it reacts with the contaminants. For example, if sulfur dioxide is the predominant contaminant to be removed, lime may turn into gypsum, which can be captured for use in other processes. As used herein, “gypsum” refers to compounds including calcium sulfate dehydrate (CaSO4.2H2O).
- Carbon
dioxide capture chamber 100 can be a conventional apparatus for removing carbon dioxide by bringing a mixture containing carbon dioxide, e.g., gaseous mixture 108, into contact with lime or slaked lime to generate limestone. For example, carbondioxide capture chamber 100 can include a chamber, a tube, a container, or the like having holes that allow passage of carbon dioxide into and out of the chamber, tube, container, or the like. Carbondioxide capture chamber 100 can also include a fluidized bed or circulating fluidized bed wherein lime or slaked lime are suspended on an upward blowing stream of carbon dioxide. In some embodiments, a bubbling fluidized bed can be utilized. Carbondioxide capture chamber 100 can also include cyclones (not shown) that separate the solids and residual exhaust or flue gas before discharging any exhaust to the atmosphere via astack 127. As further discussed below, the lime or slaked lime used in carbondioxide capture chamber 100 can be generated insorbent regenerator 102. -
Sorbent regenerator 102 is used to generate lime and carbon dioxide from the limestone generated in carbondioxide capture chamber 100. In some embodiments,sorbent regenerator 102 includes aconduit 128 for providing lime generated to carbondioxide capture chamber 100. In some embodiments,sorbent regenerator 102 includes a conduit (not shown) for providing any excess lime generated toboiler 92 andcombustion zone 104 for combustion. In some embodiments,sorbent regenerator 102 is a low emission kiln such as reducedemission kiln 20, which is described above. - In some embodiments,
system 90 includes additional heat exchangers (not shown) for capturing heat generated insorbent regenerator 102. For example, where reducedemission kiln 20 is included insystem 90, heat exchangers for capturing heat fromcalcination zone 24 andcombustion zones - In some embodiments,
system 90 is used to heat steam and drive turbines to generate electricity. Heated gaseous mixture 108 can indirectly heatpipes 130 containing, for example, steam, which can then drive one or more turbines (not shown) to generate power, such as electricity. - With minor variations for particular applications, e.g., variations in feed materials and operation temperatures, uses for an oxygen-blown reduced emission kiln according to the disclosed subject matter include, but are not limited to the following: the production of lime, clinker, and cement with reduced carbon dioxide emissions; reducing the emissions from power plants that run on coal or one or more fossil fuels; reducing carbon dioxide emissions from iron and steel blast furnaces; reducing emissions for paper production processes; for performing Fischer-Tropsch processes with reduced carbon dioxide emissions; and reducing carbon dioxide emissions in a system used for the heat treatment of solids or the volatilization of pollutants, such as a soil remediation method in which soil is burned to oxidize pollutants. For example, an oxygen-blown reduced emission kiln according to the disclosed subject matter can be utilized to capture the carbon dioxide gases contained in the exhaust gas of one or more of the processes described above.
- Although the disclosed subject matter has been described and illustrated with respect to embodiments thereof, it should be understood by those skilled in the art that features of the disclosed embodiments can be combined, rearranged, etc., to produce additional embodiments within the scope of the invention, and that various other changes, omissions, and additions may be made therein and thereto, without parting from the spirit and scope of the present application.
Claims (20)
1. A reduced emission kiln, said kiln comprising:
a combustion zone for generating a heat energy, said combustion zone including an oxygen inlet and a fuel inlet; and
a calcination zone for converting limestone into lime and carbon dioxide in response to said heat energy from said combustion zone, said calcination zone including an inlet for limestone, a conduit for directing the carbon dioxide to said combustion zone for use as a flood gas to control said heat energy, an outlet for directing the lime to a hydration chamber, and a carbon dioxide permeable membrane for separating the carbon dioxide in said calcination zone from other materials in said calcination zone and preventing the other materials from entering said conduit for directing the carbon dioxide.
2. The kiln according to claim 1 , further comprising a hydration chamber for hydrating the lime received from said outlet for directing the lime, wherein the lime is converted to slaked lime in said hydration chamber.
3. The kiln according to claim 1 , further comprising means for capturing the carbon dioxide present in said calcination zone.
4. The kiln according to claim 1 , further comprising a gasification zone for gasifying fuels to be combusted in said combustion zone, said gasification zone including a fuel inlet and a conduit for directing the gasified fuels to said combustion zone.
5. The kiln according to claim 1 , further comprising a preheating zone for preheating limestone, said preheating zone including a conduit for directing preheated limestone to said calcination zone.
6. The kiln according to claim 5 , further comprising a conduit for directing said heat energy from said combustion zone to said preheating zone.
7. The kiln according to claim 1 , wherein a carbonaceous fuel is combusted in said combustion zone.
8. A method of reducing emissions from a kiln, said method comprising:
providing a carbonaceous fuel and oxygen;
combusting said carbonaceous fuel and oxygen to form a gaseous mixture including carbon dioxide, said gaseous mixture providing a heat energy;
providing limestone;
mixing said gaseous mixture with said limestone thereby heating said limestone with said heat energy;
converting said limestone to lime and carbon dioxide;
separating carbon dioxide from said lime and from other materials in said gaseous mixture; and
mixing at least a portion of the carbon dioxide separated from said lime and from other materials in said gaseous mixture with said carbonaceous fuel and oxygen while combusting said carbonaceous fuel and oxygen thereby controlling said heat energy.
9. The method according to claim 8 , further comprising:
hydrating said lime.
10. The method according to claim 8 , further comprising:
capturing at least a portion of said carbon dioxide separated from said lime and from other materials in said gaseous mixture.
11. The method according to claim 8 , further comprising:
gasifying said carbonaceous fuel prior to combusting.
12. The method according to claim 8 , further comprising:
preheating limestone prior to converting.
13. The method according to claim 12 , further comprising:
preheating limestone with said heat energy.
14. A reduced emission combustion system, said system comprising:
a boiler including a combustion zone for combusting carbonaceous fuels to form a gaseous mixture, said gaseous mixture providing a heat energy;
a particle separator for removing fly ash and other particulates from said gaseous mixture;
a calcium-based heat exchanger configured to mix and heat steam and slaked lime to form lime and steam, configured to capture the exothermic heat of reaction when the lime reacts to form slaked lime, and configured to recycle the slaked lime to the beginning of said calcium-based heat exchange system, said calcium-based heat exchange system including means for collecting dissolved slaked lime;
a dry or wet scrubber for removing contaminants present in said gaseous mixture, said dry or wet scrubber including means for utilizing said dissolved slaked lime from said calcium-based heat exchange system;
a carbon dioxide removal chamber for removing carbon dioxide present in said gaseous mixture, said carbon dioxide removal chamber including means for bringing said gaseous mixture into contact with lime or slaked lime to generate limestone; and
a sorbent regenerator for generating lime and carbon dioxide from said limestone generated in said carbon dioxide removal chamber, said sorbent regenerator including means for providing said lime generated to said carbon dioxide removal chamber.
15. The system according to claim 14 , wherein said sorbent regenerator is a low emission kiln comprising:
a combustion zone for generating a heat energy, said combustion zone including an oxygen inlet and a fuel inlet; and
a calcination zone for converting limestone into lime and carbon dioxide in response to said heat energy from said combustion zone, said calcination zone including an inlet for limestone, a conduit for directing the carbon dioxide to said combustion zone for use as a flood gas to control said heat energy, an outlet for directing the lime to a hydration chamber, and a carbon dioxide permeable membrane for separating the carbon dioxide in said calcination zone from other materials in said calcination zone and preventing the other materials from entering said conduit for directing the carbon dioxide.
16. The system according to claim 15 , further comprising:
a heat exchanger for capturing heat from said calcination zone.
17. The system according to claim 15 , further comprising:
a heat exchanger for capturing heat from said combustion zone.
18. The system according to claim 15 , further comprising:
means for feeding lime generated in said calcination zone to said combustion zone.
19. The system according to claim 14 , further comprising means for generating electricity.
20. The system according to claim 19 , wherein said means for generating electricity include a turbine system.
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