US20120308941A1 - Method and device for high-temperature combustion using fuel and aqueous solution of organic compound - Google Patents
Method and device for high-temperature combustion using fuel and aqueous solution of organic compound Download PDFInfo
- Publication number
- US20120308941A1 US20120308941A1 US13/520,690 US201113520690A US2012308941A1 US 20120308941 A1 US20120308941 A1 US 20120308941A1 US 201113520690 A US201113520690 A US 201113520690A US 2012308941 A1 US2012308941 A1 US 2012308941A1
- Authority
- US
- United States
- Prior art keywords
- temperature
- organic compound
- aqueous solution
- burner
- combustion chamber
- 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
- 238000002485 combustion reaction Methods 0.000 title claims abstract description 117
- 150000002894 organic compounds Chemical class 0.000 title claims abstract description 89
- 239000007864 aqueous solution Substances 0.000 title claims abstract description 86
- 239000000446 fuel Substances 0.000 title claims abstract description 69
- 238000000034 method Methods 0.000 title claims abstract description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 78
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 66
- 239000000243 solution Substances 0.000 claims abstract description 32
- 239000000567 combustion gas Substances 0.000 claims abstract description 14
- 230000003028 elevating effect Effects 0.000 claims abstract description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 78
- 238000010438 heat treatment Methods 0.000 claims description 45
- 239000007789 gas Substances 0.000 claims description 28
- 239000003921 oil Substances 0.000 claims description 27
- 238000005507 spraying Methods 0.000 claims description 20
- 238000009841 combustion method Methods 0.000 claims description 19
- 230000037361 pathway Effects 0.000 claims description 12
- 150000001298 alcohols Chemical class 0.000 claims description 9
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 8
- 238000009835 boiling Methods 0.000 claims description 6
- 239000000919 ceramic Substances 0.000 claims description 6
- 239000003350 kerosene Substances 0.000 claims description 6
- 239000003208 petroleum Substances 0.000 claims description 6
- 239000007921 spray Substances 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 238000000354 decomposition reaction Methods 0.000 claims description 4
- 150000002576 ketones Chemical class 0.000 claims description 4
- 239000003915 liquefied petroleum gas Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 239000003345 natural gas Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 231100000331 toxic Toxicity 0.000 claims description 4
- 230000002588 toxic effect Effects 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 235000005985 organic acids Nutrition 0.000 claims description 3
- KVGZZAHHUNAVKZ-UHFFFAOYSA-N 1,4-Dioxin Chemical compound O1C=COC=C1 KVGZZAHHUNAVKZ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001299 aldehydes Chemical class 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 3
- 230000001476 alcoholic effect Effects 0.000 abstract 1
- 239000000295 fuel oil Substances 0.000 description 32
- 238000006243 chemical reaction Methods 0.000 description 10
- 238000004880 explosion Methods 0.000 description 8
- 239000002351 wastewater Substances 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 5
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
- 239000010815 organic waste Substances 0.000 description 4
- 238000010248 power generation Methods 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000004868 gas analysis Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- -1 aldehyde ketones Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000010794 food waste Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/08—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating
- F23G5/085—High-temperature heating means, e.g. plasma, for partly melting the waste
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/08—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating
- F23G5/12—Incineration of waste; Incinerator constructions; Details, accessories or control therefor having supplementary heating using gaseous or liquid fuel
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/44—Details; Accessories
- F23G5/46—Recuperation of heat
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G5/00—Incineration of waste; Incinerator constructions; Details, accessories or control therefor
- F23G5/50—Control or safety arrangements
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
- F23G7/001—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals for sludges or waste products from water treatment installations
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
- F23G7/008—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals for liquid waste
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
- F23G7/04—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of waste liquors, e.g. sulfite liquors
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23M—CASINGS, LININGS, WALLS OR DOORS SPECIALLY ADAPTED FOR COMBUSTION CHAMBERS, e.g. FIREBRIDGES; DEVICES FOR DEFLECTING AIR, FLAMES OR COMBUSTION PRODUCTS IN COMBUSTION CHAMBERS; SAFETY ARRANGEMENTS SPECIALLY ADAPTED FOR COMBUSTION APPARATUS; DETAILS OF COMBUSTION CHAMBERS, NOT OTHERWISE PROVIDED FOR
- F23M9/00—Baffles or deflectors for air or combustion products; Flame shields
- F23M9/06—Baffles or deflectors for air or combustion products; Flame shields in fire-boxes
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN A CARRIER GAS OR AIR
- F23C2900/00—Special features of, or arrangements for combustion apparatus using fluid fuels or solid fuels suspended in air; Combustion processes therefor
- F23C2900/9901—Combustion process using hydrogen, hydrogen peroxide water or brown gas as fuel
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2204/00—Supplementary heating arrangements
- F23G2204/10—Supplementary heating arrangements using auxiliary fuel
- F23G2204/103—Supplementary heating arrangements using auxiliary fuel gaseous or liquid fuel
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2206/00—Waste heat recuperation
- F23G2206/20—Waste heat recuperation using the heat in association with another installation
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2207/00—Control
- F23G2207/10—Arrangement of sensing devices
- F23G2207/101—Arrangement of sensing devices for temperature
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2900/00—Special features of, or arrangements for incinerators
- F23G2900/50006—Combustion chamber walls reflecting radiant energy within the chamber
Definitions
- the present invention relates to a method and a device for combustion of an aqueous solution of an organic compound.
- it relates to a method and a device for high-temperature combustion in which an aqueous solution of an organic compound like an aqueous alcohol solution and fuel are used.
- examples of the organic compound for an aqueous solution of an organic compound include alcohols, organic acids, and aldehyde ketones.
- examples of the organic aqueous solution include organic waste water, which is an industrial waste.
- a common practice includes that an organic aqueous solution is slowly added thereto for combustion while heavy oil or the like is burned with a burner. According to this method, the organic compounds contained in an organic waste water are oxidized while water contained in the organic waste water is vaporized by burning heavy oil, and as it has almost no contribution in terms of energy, it is just practiced as a simple way of processing waste water.
- the fuels used for an incinerator or an internal combustion engine is mostly a water-in-oil (W/O) type emulsion.
- W/O water-in-oil
- oils in water-in-oil (W/O) type are exposed to surface, and therefore there is a merit that it is easily combustible.
- oils are included as microparticles in water, and therefore there is a problem that it is much less combustible.
- the water vapor explosion does not occur when extremely rapid heat transfer is not allowed.
- the heat transfer occurs about 5 times faster in an O/W type than a W/O type, and therefore it has greater chance to have water vapor explosion.
- the water vapor explosion may occur when molten iron is dropped into a water bath or underground water is in contact with magma (see, Science of Vapor Explosion (written by TAKASHIMA Takeo and IIDA Yoshihiro, SHOKABO Publishing Co., Ltd. published on Jan. 25, 1998, pages 28 to 57).
- an object of the invention is to accomplish improvement of combustion efficiency by having a condition at which water vapor explosion (i.e., microexplosion of sprayed particles or the like) is guaranteed to occur, decomposing organic compounds contained in water by utilizing the energy of microexplosion of water vapor, and promoting an aqueous gas reaction with water molecules and an oxidation reaction with air.
- water vapor explosion i.e., microexplosion of sprayed particles or the like
- droplets of sprayed organic aqueous solution are sprayed into a high temperature environment to cause microexplosion of water vapor, and according to decomposition of an organic compound contained in the organic aqueous solution, an aqueous gas reaction and an oxidation reaction occur to reduce an endothermic reaction of an aqueous gas reaction (i.e., an endothermic reaction is reduced when chemical bonds are broken or the like), and consequently combustion efficiency increases.
- a high-temperature combustion method using fuels and an aqueous solution of an organic compound including: in a combustion chamber, (1) spraying and burning a fuel with a first burner to heat the interior temperature of a combustion chamber to a high temperature of 700° C. or above; and (2) spraying subsequently an aqueous solution of an organic compound with a second burner into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature.
- a high-temperature combustion method using fuels and an aqueous solution of an organic compound including: (1) spraying and burning in a combustion chamber a fuel with a first burner to heat the interior temperature of the combustion chamber to a high temperature of 700° C.
- a device for high-temperature combustion using fuels and an aqueous solution of an organic compound including (1) a combustion chamber, (2) a first burner attached thereto to spray and burn a fuel in the inside of the combustion chamber so that the interior temperature of the combustion chamber is heated to a high temperature of 700° C. or above, and (3) a second burner which is attached close to the first burner and used for spraying an aqueous solution of an organic compound into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature.
- a device for high-temperature combustion using fuels and an aqueous solution of an organic compound including (1) a combustion chamber, (2) a first burner attached thereto to spray and burn a fuel in the inside of the combustion chamber so that the interior temperature of the combustion chamber is heated to a high temperature of 700° C. or above, (3) a second burner which is attached close to the first burner and used for spraying an aqueous solution of an organic compound into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature, and (4) a chamber for heat treatment which is installed to be connected to the combustion chamber.
- the fuel sprayed with the first burner is any one or more types that are selected from petroleum oils like kerosene oil and light oil, organic solvents like alcohols, city gas, LPG, natural gas, hydrogen gas, and brown gas.
- a fuel is sprayed and burned with a first burner to elevate the interior temperature of the combustion chamber to a high temperature of 700° C. or above, and an aqueous solution of an organic compound is subsequently sprayed with a second burner into the high-temperature combustion gas obtained with the first burner, consequently causing mixing and burning.
- interior temperature of the combustion chamber and/or temperature of a chamber for heat treatment can be synergistically increased to high temperature. As such, the fuels and organic compounds are fully burned, and thus the fuel cost can be reduced.
- FIG. 1 is a frontal view for describing the device of Example 1 of the invention
- FIG. 2A is a cross-sectional view for illustrating the combustion chamber in the device of Example 1 and FIGS. 2B and 2C are plane views for illustrating a heat resistant reflector which is placed in the combustion chamber;
- FIG. 3 is a graph for illustrating the temperature change in the device of Example 1;
- FIG. 4 is a graph for illustrating the temperature change in the device of Example 2.
- FIG. 5 is a graph for illustrating the heat calorie generated in the device of Example 2.
- FIG. 6 is a graph for illustrating the temperature change in the device of Example 3.
- FIG. 7 is a graph for illustrating the heat calorie generated in the device of Example 3.
- FIG. 8 is a graph for illustrating the temperature change in the device of Example 4.
- FIG. 9 is a graph for illustrating the temperature change in the device of Example 5.
- FIG. 10 is a graph for illustrating the temperature change in the device of Example 6.
- FIG. 11 is a graph for illustrating the temperature change in the device of Example 7.
- FIG. 12 is a graph for illustrating the temperature change in the device of Example 8.
- FIG. 13 is a graph for illustrating the temperature change in the device of Example 9.
- FIG. 1 is a frontal view for describing the high-temperature combustion device of the example of the invention.
- reference numeral 1 indicates a combustion chamber
- reference numeral 2 indicates a first burner
- reference numeral 3 indicates a second burner
- reference numeral 101 indicates a wall of a combustion chamber
- reference numeral 201 indicates a chamber for heat treatment
- reference numeral 301 indicates a pathway
- reference numerals T 1 to T 3 indicate a thermometer.
- FIG. 2A is a cross-sectional view for illustrating the combustion chamber 1 of FIG. 1 .
- a ceramic heat resistant reflectors 4 and 5 FIGS. 2B and 2C ) having several holes 4 ′ and notch parts 5 ′ are vertically installed within the combustion chamber 1 .
- FIGS. 2B and 2C are plane views of the heat resistant reflectors 4 and 5 .
- fuel oils like heavy oil A, light oil, and kerosene oil are typically sprayed from the first burner (fuel burner) 2 into the combustion chamber 1 and burned therein.
- fuel burner fuel burner
- an amount suitable for complete combustion is supplied with the same fuels and the air ratio is generally in the range of from about 1.3 to 1.7.
- the heat resistant reflectors for example, silicon carbide based ceramic plate of which surface is coated with alumina
- the heat resistant reflectors 4 and 5 which are disposed and installed inside the combustion chamber 1 , are heated to a high temperature of 700° C. or above.
- the heat resistant reflector 4 or 5 one type or a combination of two or more types may be used.
- an organic aqueous solution (water containing an organic compound) is sprayed from the second burner (burner for spraying an aqueous solution of an organic compound) 3 so that it can be mixed with fire flame of the first burner within the combustion chamber 1 and collided with the heat resistant reflectors 4 and 5 which are heated to high temperature, and as a result, the organic compounds are decomposed and oxidized accompanied with water vapor explosion on the surfaces of the heat resistant reflectors 4 and 5 .
- thermometer T 1 the interior temperature of the combustion chamber 1 is constantly monitored.
- the high-temperature gas within a pathway 301 and a chamber for heat treatment 201 is also a high-temperature and superheated steam containing water vapor.
- thermometer T 1 As for the combustion method, heavy oil A or the like is first sprayed from the first burner 2 and burned to heat the heat resistant reflectors 4 and 5 .
- the temperature of the thermometer T 1 reaches 700° C. or above for having an aqueous gas reaction, or possibly 1000° C. or above, the organic aqueous solution starts to be sprayed.
- Spraying of the organic aqueous solution is preferably started with an amount which is the same as the fuels. However, if the temperature is as high as 1000° C., it can be also sprayed in an amount of 2 to 5 times.
- the sprayed organic aqueous solution (water containing an organic compound) is collided with the heat resistant reflectors 4 and 5 , and after sprayed water instead of vapor film on the surface receives the heat directly from the heat resistant reflectors 4 and 5 heated to a high temperature, water vapor microexplosion occurs.
- a W/O type emulsion is used instead of an organic aqueous solution, heat transfer becomes slow, and as a result, possibility of having water vapor microexplosion is extremely low.
- Water containing methanol or ethanol in an organic aqueous solution forms an azeotropic mixture with methanol or ethanol to lower the boiling point.
- the water vapor microexplosion can occur more easily.
- methanol and ethanol are soluble in water and also alcohols are inside of water cluster to get dissolved therein, in accordance with water vapor microexplosion, alcohols undergo partial decomposition or have weak bonding, and having the aqueous gas reaction and oxidation reaction at the same time, combustion with high efficiency can be achieved.
- a device having a combustion chamber 1 to which a chamber for heat treatment 201 is connected is used as illustrated in the frontal view of FIG. 1 .
- combustion chamber 1 and the chamber for heat treatment 201 are connected to each other via a pathway 301 with reduced diameter, which connects an exit of the combustion chamber 1 and an entrance of the chamber for heat treatment 201 .
- a first burner 2 for elevating the interior temperature to a high temperature of 700° C. or above and a second burner 3 for spraying an aqueous solution of an organic compound are installed.
- thermometers are placed at three spots in the device, that is, a first thermometer T 1 is placed in the combustion chamber 1 , a second thermometer T 2 is placed in the pathway 301 , and a third thermometer T 3 is placed in the chamber for heat treatment 201 .
- the chamber for heat treatment 201 is a place for utilizing heat under various purposes and power generation, running a boiler, metal refining, quenching, and incinerating food waste or the like are performed therein.
- a burner is directly attached to a chamber for heat treatment.
- a combustion chamber is prepared separately and fuels are burned in a small combustion chamber. After heating to the temperature of 700° C. or above, preferably 1000° C. or above, an aqueous solution of an organic compound like an aqueous alcohol solution is sprayed to cause water vapor microexplosion, and as result high-temperature gas is produced and transported to the chamber for heat treatment 201 to be utilized for power generation or the like.
- heavy oil A was sprayed at 5.9 L/H from the first burner 2 (air ratio: 1.5) to pre-heat the combustion chamber 1 .
- thermometer T 2 After 20 minutes, the thermometer T 2 showed 1010° C., indicating temperature increase of 210° C.
- thermometer T 3 temperature of the chamber for heat treatment 201 (the thermometer T 3 ) increased by 170° C. from 610° C. to 780° C.
- thermometer T 2 showed 980° C., indicating an increase of 180° C. and the thermometer T 3 showed 750° C., indicating an increase of 140° C.
- FIG. 3 a graph illustrating the temperature change inside the device.
- the high-temperature gas within the pathway 301 and the chamber for heat treatment 201 is high-temperature and superheated steam containing a large amount of water vapor.
- heavy oil A was sprayed at 6.6 L/H (5.7 kg/H) from a first burner 2 to heat a combustion chamber 1 . After heating for about one hour, temperature of a chamber for heat treatment 201 was 630° C. as measured by T 3 .
- temperature of the chamber for heat treatment 201 showed an increase of only 130° C., i.e., from 630° C. to 760° C.
- the chamber for heat treatment 201 Since the chamber for heat treatment 201 is used as a heating device for actual industrial use, the temperature increase in the chamber for heat treatment 201 is most critical in terms of thermal efficiency.
- Specific heat of gases is as follows: CO 2 0.54 kcal/m 3 , H 2 O (water vapor) 0.46 kcal/m 3 , O 2 0.35 kcal/m 3 , N 2 0.35 kcal/m 3 .
- Gas analysis after burning heavy oil is as follows: CO 2 8.4%, H 2 O 8.8%, O 2 6.4%, N 2 76.4% and the specific heat of gas was 0.376.
- Gas analysis after burning heavy oil+ethanol is as follows: CO 2 11.6%, H 2 O 13.8%, O 2 0.8%, N 2 73.7% (when ethanol is added, air was not particularly introduced, and therefore 6.4% of residual O 2 was consumed by burning heavy oil, lowering O 2 to 0.8%), and specific heat of gas was 0.387.
- the heat calorie of the heavy oil+30% by volume aqueous ethanol solution was increased by 23% compared to the heat calorie of heavy oil+pure ethanol in the same amount.
- the high-temperature gas (about 900 to 1100° C.) obtained in this example contains a large amount (23.8%) of H 2 O (water), and it is also high-temperature and superheated steam.
- Example 2 The test was carried out in the same manner as Example 2 for 30% by volume aqueous methanol solution and pure methanol in the same amount.
- thermometer T 2 in the pathway connecting the exit of a combustion chamber reached 800° C. and exhibited an almost stable state.
- 30% by volume aqueous methanol solution was sprayed at 15.2 L/H (pure methanol 4.6 L/H and water 10.6 L/H) from a second burner 3 .
- the thermometer T 2 in the pathway connecting the exit of a combustion chamber showed 940° C., indicating a temperature increase of 140° C.
- a thermometer T 3 in a chamber for heat treatment showed a temperature increase of 130° C., i.e., from 630° C. to 760° C.
- thermometer T 2 in the pathway connecting the exit of a combustion chamber showed a temperature increase of 140° C., i.e., from 800° C. to 940° C., which is the same increase as the 30% by volume aqueous methanol solution.
- thermometer T 3 in the chamber for heat treatment increased from 630° C. to 720° C. only.
- the utilization of heat in a boiler for power generation or an incinerator is determined by the temperature and flow amount (heat flow amount) of a chamber for heat treatment, it is found by calculation that the heat calorie in a chamber for heat treatment is increased by about 19% in the case in which 30% by volume aqueous methanol solution is added compared to the case in which pure methanol is added in the same amount.
- FIG. 7 illustrates such results.
- the high-temperature gas within the pathway 301 and the chamber for heat treatment 201 was high-temperature and superheated steam containing a large amount of high-temperature water vapor.
- thermometer T 1 measures the temperature at the center of the combustion chamber
- thermometer T 2 measures the temperature at the exit of the combustion chamber
- thermometer T 3 measures the temperature around the exit of the chamber for heat treatment. Since the chamber for heat treatment is a place for multipurpose use, it is expected to be used for power generation, or as a boiler or an incinerator or the like. Thus, the thermal efficiency will be improved more as the temperature of the thermometer T 3 increases.
- thermometer T 2 showed a temperature increase of 120° C., i.e., from 960° C. to 1080° C. and the thermometer T 3 showed a temperature increase of 100° C., i.e., from 800° C. to 900° C.
- the results are as illustrated in FIG. 8 .
- Example 2 the same device ( FIG. 1 ) as Example 1 was used.
- Heavy oil A was used at 6.6 L/H and the pre-heating time was 30 minutes.
- 30% by volume aqueous methanol solution was sprayed at 25 L/H.
- thermometer T 2 showed a temperature increase of 135° C., i.e., from 965° C. to 1100° C. and the thermometer T 3 showed a temperature increase of 130° C., i.e., from 810° C. to 940° C. Since the spray amount of 30% by volume aqueous methanol solution was different between Example 4 and Example 5, i.e., 21 L/H and 25 L/H, respectively, the temperature increase measured by the thermometer T 3 was also different, i.e., Example 4: 900° C. (+100° C.) and Example 5: 940° C. (+130° C.). The results are as illustrated in FIG. 9 .
- heavy oil A was sprayed at 6.6 L/H from a first burner 2 to heat the inside of a combustion chamber 1 to 700° C. or above, and then 30% by volume aqueous ethanol solution was sprayed at 15.2 L/H from a second burner 3 (ethanol 4.6 L+water 106 L).
- thermometer T 2 showed a rapid temperature increase of 220° C., i.e., from 780° C. to 1000° C. and the thermometer T 3 showed a temperature increase of 190° C., i.e., from 630° C. to 820° C. Eight minutes later, heavy oil A was reduced by 23%, i.e., from 6.6 to 5.1 L/H, and as a result, the thermometer T 2 was recovered to the level before the addition of ethanol. Meanwhile, although the thermometer T 3 also showed a decrease of 70° C., indicating the temperature of 730° C., but it is still 110° C. higher than the level before the addition of ethanol. The results are as illustrated in FIG. 10 .
- Example 6 The test was carried out under the same condition as Example 6 to determine the reproducibility. First, to heat a combustion chamber to 700° C. or above, heavy oil A was sprayed at 6.6 L/H from a first burner 1 to increase the temperature of the combustion chamber.
- thermometer T 2 and the thermometer T 3 showed 800° C. and 640° C., respectively. At that time, 30% by volume aqueous ethanol solution was sprayed at 15.2 L/H.
- thermometer T 2 showed 980° C., representing a temperature increase of 180° C. and the thermometer T 3 showed 800° C., representing a temperature increase of 160° C.
- thermometer T 2 at the exit of the combustion chamber showed a temperature decrease of 160° C., i.e., from 980° C. to 820° C. and the thermometer T 3 at the exit of the chamber for heat treatment showed a temperature decrease of only 70° C., i.e., from 800° C. to 730° C. (however, there is still a difference of 90° C. compared to the temperature of 640° C. obtained originally from heavy oil A only).
- the results are as illustrated in FIG. 11 .
- the amount of heavy oil A may be further reduced by 22%, thus it is believed that overall 44% reduction can be achieved.
- Example 8 it was added in an amount of 10.6 L/H in Example 8, compared to 21 L/H and 25 L/H in Example 4 and Example 5, respectively.
- thermometer T 2 showed a temperature increase of 135° C., i.e., from 800° C. to 935° C. and the thermometer T 3 showed a temperature increase of only 125° C., i.e., from 625° C. to 745° C. in this example.
- the amount of heavy oil A may be further reduced by 17%, thus it is believed that overall 34% reduction can be achieved.
- test was carried out by adding methanol-based waste water (i.e., waste water containing 40% by volume of methanol and slight amount of others like amine and formalin).
- methanol-based waste water i.e., waste water containing 40% by volume of methanol and slight amount of others like amine and formalin.
- heavy oil A was sprayed at 5.7 L/H from a first burner 2 into a combustion chamber 1 and burned therein followed by heating for about 70 minutes.
- thermometer T 1 of the combustion chamber shows 1050° C.
- thermometer T 2 at the exit of the combustion chamber shows 750° C.
- the methanol-based waste water was added and burned at 11.4 L/H with a second burner 3 .
- the temperature was increased by about 200° C.
- the thermometer T 2 showed an increase of 230° C., i.e., from 750° C. to 980° C. The results are as illustrated in FIG. 13 .
- the temperature of a chamber for heat treatment which can be used as a thermal engine, showed an increase of 160° C., i.e., from 600° C. to 760° C.
- the methanol-based organic waste water can be used for the invention.
- waste water containing methanol in an amount of 40% by volume or so is handed over to a waste water management company with charge since the waste water is not burned as it is.
- a waste water management company with charge since the waste water is not burned as it is.
- it may be fully utilized as a fuel and also a cost required for handing over to a waste management company can be saved.
- the high-temperature gas within the pathway 301 and the chamber for heat treatment 201 was also high-temperature and superheated steam containing a large amount of water vapor.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Spray-Type Burners (AREA)
Abstract
A method and a device are disclosed with which high-temperature combustion is attained using a fuel and an aqueous solution of an organic compound, e.g., an aqueous alcohol solution. In a combustion chamber, a fuel is sprayed and burned with a first burner to elevate the interior temperature of the combustion chamber (and/or a heat-resistant reflector disposed inside the combustion chamber) to a high temperature of 700° C. or above, and an aqueous solution of an organic compound (e.g., an alcohol-water mixture) is subsequently sprayed with a second burner into the high-temperature combustion gas obtained with the first burner, thereby causing microexplosion of water vaper and further elevating the interior temperature. As such, the fuels and organic compounds (e.g., Alcoholic aqueous solution) are fully burned, and thus the fuel cost can be reduced. Thus, high-temperature superheated steam containing a large amount of water vapor is yielded.
Description
- 1. Field of the Invention
- The present invention relates to a method and a device for combustion of an aqueous solution of an organic compound. In particular, it relates to a method and a device for high-temperature combustion in which an aqueous solution of an organic compound like an aqueous alcohol solution and fuel are used.
- 2. Description of the Related Art
- With regard to a conventional method for combustion by using liquid fuel and adding hydrous fuel containing an organic compound, examples of the organic compound for an aqueous solution of an organic compound (hereinbelow, referred to as an “organic aqueous solution”) include alcohols, organic acids, and aldehyde ketones. Examples of the organic aqueous solution include organic waste water, which is an industrial waste.
- For combustion of an organic aqueous solution, a common practice includes that an organic aqueous solution is slowly added thereto for combustion while heavy oil or the like is burned with a burner. According to this method, the organic compounds contained in an organic waste water are oxidized while water contained in the organic waste water is vaporized by burning heavy oil, and as it has almost no contribution in terms of energy, it is just practiced as a simple way of processing waste water.
- There is also a method including adding and mixing heavy oil or the like to an organic aqueous solution to give a water-in-oil (W/O) type emulsion and processing it as fuel. However, according to this method, although the organic compounds contained in an organic aqueous solution can be utilized as fuel, it does not provide any particularly efficient combustion.
- In a case in which an emulsion type hydrous fuel is burned, the fuels used for an incinerator or an internal combustion engine is mostly a water-in-oil (W/O) type emulsion. According to this type, oils in water-in-oil (W/O) type are exposed to surface, and therefore there is a merit that it is easily combustible. On the other hand, according to an oil droplet in water (O/W) type, oils are included as microparticles in water, and therefore there is a problem that it is much less combustible.
- However, with regard to thermal conductivity of petroleum oils and water, water has a thermal conductivity of 0.674 W/mk at 360° K (87° C.) while decane (C10H22), which is one type of oils included in petroleum oils, has a thermal conductivity of 0.119 W/mk at the same temperature. As such, it is known that water has a thermal conductivity which is 5.6 times larger than that of decane (see, Handbook of Chemistry, Basics II (Maruzen Company, Limited, published on Jun. 25, 1984, page 73).
- Meanwhile, with regard to a condition for water vapor explosion, the water vapor explosion does not occur when extremely rapid heat transfer is not allowed. Thus, under the exactly same condition, the heat transfer occurs about 5 times faster in an O/W type than a W/O type, and therefore it has greater chance to have water vapor explosion.
- Further, it is also described that the water vapor explosion may occur when molten iron is dropped into a water bath or underground water is in contact with magma (see, Science of Vapor Explosion (written by TAKASHIMA Takeo and IIDA Yoshihiro, SHOKABO Publishing Co., Ltd. published on Jan. 25, 1998, pages 28 to 57).
- Even when a W/O type emulsion is sprayed, surface of the emulsion is covered with oils, and therefore thermal conductivity is small. Further, as the surface of oils is covered with oil vapor film (in general, thermal conductivity of a gas is only 1/10 or less than that of a liquid), a possibility of having water vapor explosion is extremely low.
- In view of the knowledge described above, an object of the invention is to accomplish improvement of combustion efficiency by having a condition at which water vapor explosion (i.e., microexplosion of sprayed particles or the like) is guaranteed to occur, decomposing organic compounds contained in water by utilizing the energy of microexplosion of water vapor, and promoting an aqueous gas reaction with water molecules and an oxidation reaction with air.
- First, with regard to the condition at which water vapor microexplosion occurs, it involves instantaneous temperature increase of an organic aqueous solution to high temperature, and for example, water vapor microexplosion is caused by collision on surface of a solid at high temperature.
- If no water vapor microexplosion occurs, only a simple aqueous gas reaction of water vapor and organic compounds contained in an organic aqueous solution and an oxidation reaction of air will occur, and therefore it is difficult to expect a significant increase in combustion efficiency. According to the invention, droplets of sprayed organic aqueous solution are sprayed into a high temperature environment to cause microexplosion of water vapor, and according to decomposition of an organic compound contained in the organic aqueous solution, an aqueous gas reaction and an oxidation reaction occur to reduce an endothermic reaction of an aqueous gas reaction (i.e., an endothermic reaction is reduced when chemical bonds are broken or the like), and consequently combustion efficiency increases. In fact, when a 40% by volume aqueous alcohol solution is sprayed on a heat resistant iron reflector with holes, which is heated to 850° C., the heat resistant iron reflector is melted to give a molten mass. Thus, it is believed that water vapor microexplosion, an aqueous gas reaction, and an oxidation reaction occur simultaneously to cause instantaneous temperature increase.
- Under the circumstances described above, inventors of the present invention conducted intensive studies, and as a result, were able to solve the problems with the means given below.
- [1] A high-temperature combustion method using fuels and an aqueous solution of an organic compound, including: in a combustion chamber, (1) spraying and burning a fuel with a first burner to heat the interior temperature of a combustion chamber to a high temperature of 700° C. or above; and (2) spraying subsequently an aqueous solution of an organic compound with a second burner into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature.
[2] A high-temperature combustion method using fuels and an aqueous solution of an organic compound, including: (1) spraying and burning in a combustion chamber a fuel with a first burner to heat the interior temperature of the combustion chamber to a high temperature of 700° C. or above; (2) spraying subsequently in the combustion chamber an aqueous solution of an organic compound with a second burner into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature; and (3) burning completely in a chamber for heat treatment, which is installed to be connected to the combustion chamber, the combustion gas introduced from the combustion chamber for elevating the temperature to a high temperature.
[3] The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to the item [1] or [2], including: (1) spraying and burning in a combustion chamber a fuel with a first burner to heat a heat resistant reflector installed within the combustion chamber to 700° C. or above; and (2) spraying subsequently in the combustion chamber an aqueous solution of an organic compound with a second burner into high-temperature combustion gas obtained with the first burner followed by mixing and burning, and further elevating the interior temperature to higher temperature by colliding with the surface of the heat resistant reflector being heated.
[4] The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to the item [3], wherein the heat resistant reflector is a heat resistant metal or ceramic reflector including several holes.
[5] The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to any one of the items [1] to [4], wherein the organic compound of the aqueous solution of an organic compound has boiling point of 100° C. or less and is soluble in water.
[6] The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to any one of the items [1] to [5], wherein the organic compound of the aqueous solution of an organic compound is one or more types that are selected from water-soluble alcohols, organic acids, aldehydes, and ketones.
[7] The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to any one of the items [1] to [6], wherein the aqueous solution of an organic compound is an aqueous alcohol solution including 10 to 50% by volume of ethanol or methanol.
[8] The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to any one of the items [1] to [7], wherein the fuel sprayed with the first burner is any one or more types that are selected from petroleum oils like kerosene oil and light oil, organic solvents like alcohols, city gas, LPG, natural gas, hydrogen gas, and brown gas.
[9] The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to any one of the items [1] to [8], wherein the aqueous solution of an organic compound includes hardly-decomposable toxic materials including a benzene ring as a skeleton structure like dioxin and PCB and the benzene ring of the toxic materials are detoxified by decomposition in a combustion chamber.
[10] A method of producing high-temperature and superheated steam by using the method described in the items [1] to [9].
[11] A device for high-temperature combustion using fuels and an aqueous solution of an organic compound, including (1) a combustion chamber, (2) a first burner attached thereto to spray and burn a fuel in the inside of the combustion chamber so that the interior temperature of the combustion chamber is heated to a high temperature of 700° C. or above, and (3) a second burner which is attached close to the first burner and used for spraying an aqueous solution of an organic compound into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature.
[12] A device for high-temperature combustion using fuels and an aqueous solution of an organic compound, including (1) a combustion chamber, (2) a first burner attached thereto to spray and burn a fuel in the inside of the combustion chamber so that the interior temperature of the combustion chamber is heated to a high temperature of 700° C. or above, (3) a second burner which is attached close to the first burner and used for spraying an aqueous solution of an organic compound into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature, and (4) a chamber for heat treatment which is installed to be connected to the combustion chamber.
[13] The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to the item [12], wherein a means for connecting the combustion chamber and the chamber for heat treatment is a pathway with reduced diameter, which is installed between an exit of the combustion chamber and an entrance of the chamber for heat treatment.
[14] The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to any one of the items [11] to [13], wherein a heat resistant reflector is disposed and installed in the combustion chamber.
[15] The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to the item [14], wherein the heat resistant reflector is a metal or ceramic reflector including several holes.
[16] The method for high-temperature combustion using fuels and an aqueous solution of an organic compound according to any one of the items [11] to [15], wherein the organic compound of the aqueous solution of an organic compound has boiling point of 100° C. or less and is soluble in water.
[17] The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to any one of the items [11] to [16], wherein the aqueous solution of an organic compound sprayed with the second burner is an aqueous alcohol solution including 10 to 50% by volume of ethanol or methanol.
[18] The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to any one of the items [11] to [17], wherein the fuel sprayed with the first burner is any one or more types that are selected from petroleum oils like kerosene oil and light oil, organic solvents like alcohols, city gas, LPG, natural gas, hydrogen gas, and brown gas.
[19] A device for producing superheated steam using the device described in any one of the items [11] to [18]. - According to the invention, in a combustion chamber, a fuel is sprayed and burned with a first burner to elevate the interior temperature of the combustion chamber to a high temperature of 700° C. or above, and an aqueous solution of an organic compound is subsequently sprayed with a second burner into the high-temperature combustion gas obtained with the first burner, consequently causing mixing and burning. Thus, compared to a case in which combustion is carried out by using only fuels or an aqueous solution of an organic compound, interior temperature of the combustion chamber and/or temperature of a chamber for heat treatment can be synergistically increased to high temperature. As such, the fuels and organic compounds are fully burned, and thus the fuel cost can be reduced.
- Further, with a simple means, high-temperature and superheated steam can be produced in a large amount.
-
FIG. 1 is a frontal view for describing the device of Example 1 of the invention; -
FIG. 2A is a cross-sectional view for illustrating the combustion chamber in the device of Example 1 andFIGS. 2B and 2C are plane views for illustrating a heat resistant reflector which is placed in the combustion chamber; -
FIG. 3 is a graph for illustrating the temperature change in the device of Example 1; -
FIG. 4 is a graph for illustrating the temperature change in the device of Example 2; -
FIG. 5 is a graph for illustrating the heat calorie generated in the device of Example 2; -
FIG. 6 is a graph for illustrating the temperature change in the device of Example 3; -
FIG. 7 is a graph for illustrating the heat calorie generated in the device of Example 3; -
FIG. 8 is a graph for illustrating the temperature change in the device of Example 4; -
FIG. 9 is a graph for illustrating the temperature change in the device of Example 5; -
FIG. 10 is a graph for illustrating the temperature change in the device of Example 6; -
FIG. 11 is a graph for illustrating the temperature change in the device of Example 7; -
FIG. 12 is a graph for illustrating the temperature change in the device of Example 8; and -
FIG. 13 is a graph for illustrating the temperature change in the device of Example 9. - Hereinbelow, the preferred embodiments of the invention are explained in greater detail in view of the drawings and the examples.
-
FIG. 1 is a frontal view for describing the high-temperature combustion device of the example of the invention. Specifically,reference numeral 1 indicates a combustion chamber,reference numeral 2 indicates a first burner,reference numeral 3 indicates a second burner,reference numeral 101 indicates a wall of a combustion chamber,reference numeral 201 indicates a chamber for heat treatment,reference numeral 301 indicates a pathway, and reference numerals T1 to T3 indicate a thermometer. -
FIG. 2A is a cross-sectional view for illustrating thecombustion chamber 1 ofFIG. 1 . Specifically, a ceramic heatresistant reflectors 4 and 5 (FIGS. 2B and 2C ) havingseveral holes 4′ and notchparts 5′ are vertically installed within thecombustion chamber 1. Further,FIGS. 2B and 2C are plane views of the heat 4 and 5.resistant reflectors - First of all, fuel oils like heavy oil A, light oil, and kerosene oil are typically sprayed from the first burner (fuel burner) 2 into the
combustion chamber 1 and burned therein. As to an amount of air, an amount suitable for complete combustion is supplied with the same fuels and the air ratio is generally in the range of from about 1.3 to 1.7. - Accordingly, the heat resistant reflectors (for example, silicon carbide based ceramic plate of which surface is coated with alumina) 4 and 5, which are disposed and installed inside the
combustion chamber 1, are heated to a high temperature of 700° C. or above. As for the heat 4 or 5, one type or a combination of two or more types may be used.resistant reflector - Subsequently, an organic aqueous solution (water containing an organic compound) is sprayed from the second burner (burner for spraying an aqueous solution of an organic compound) 3 so that it can be mixed with fire flame of the first burner within the
combustion chamber 1 and collided with the heat 4 and 5 which are heated to high temperature, and as a result, the organic compounds are decomposed and oxidized accompanied with water vapor explosion on the surfaces of the heatresistant reflectors 4 and 5.resistant reflectors - The aqueous solution of an organic compound is sprayed from the
second burner 3 into thecombustion chamber 1, and the composition ratio range is as follows; organic compounds:water=1:0.5 to 20 (that is, content of the organic compounds is 66.7 to 5.0% by volume). Further, the spray amount of the aqueous solution of an organic compound from thesecond burner 3 is preferably 1 to 5 parts by volume per one part by volume of the kerosene oil sprayed from thefirst burner 2. - Further, the interior temperature of the
combustion chamber 1 is constantly monitored by a thermometer T1. - In such case, the high-temperature gas within a
pathway 301 and a chamber forheat treatment 201 is also a high-temperature and superheated steam containing water vapor. - As for the combustion method, heavy oil A or the like is first sprayed from the
first burner 2 and burned to heat the heat 4 and 5. When the temperature of the thermometer T1 reaches 700° C. or above for having an aqueous gas reaction, or possibly 1000° C. or above, the organic aqueous solution starts to be sprayed.resistant reflectors - Spraying of the organic aqueous solution is preferably started with an amount which is the same as the fuels. However, if the temperature is as high as 1000° C., it can be also sprayed in an amount of 2 to 5 times. The sprayed organic aqueous solution (water containing an organic compound) is collided with the heat
4 and 5, and after sprayed water instead of vapor film on the surface receives the heat directly from the heatresistant reflectors 4 and 5 heated to a high temperature, water vapor microexplosion occurs. In such case, if a W/O type emulsion is used instead of an organic aqueous solution, heat transfer becomes slow, and as a result, possibility of having water vapor microexplosion is extremely low.resistant reflectors - Water containing methanol or ethanol in an organic aqueous solution forms an azeotropic mixture with methanol or ethanol to lower the boiling point. As a result, the water vapor microexplosion can occur more easily. Further, since methanol and ethanol are soluble in water and also alcohols are inside of water cluster to get dissolved therein, in accordance with water vapor microexplosion, alcohols undergo partial decomposition or have weak bonding, and having the aqueous gas reaction and oxidation reaction at the same time, combustion with high efficiency can be achieved.
- In this example, a device having a
combustion chamber 1 to which a chamber forheat treatment 201 is connected is used as illustrated in the frontal view ofFIG. 1 . - Specifically, the
combustion chamber 1 and the chamber forheat treatment 201 are connected to each other via apathway 301 with reduced diameter, which connects an exit of thecombustion chamber 1 and an entrance of the chamber forheat treatment 201. - Further, in the
combustion chamber 1, afirst burner 2 for elevating the interior temperature to a high temperature of 700° C. or above and asecond burner 3 for spraying an aqueous solution of an organic compound are installed. - Further, thermometers are placed at three spots in the device, that is, a first thermometer T1 is placed in the
combustion chamber 1, a second thermometer T2 is placed in thepathway 301, and a third thermometer T3 is placed in the chamber forheat treatment 201. - Meanwhile, the chamber for
heat treatment 201 is a place for utilizing heat under various purposes and power generation, running a boiler, metal refining, quenching, and incinerating food waste or the like are performed therein. - According to a conventional technique, a burner is directly attached to a chamber for heat treatment. According to the invention, however, a combustion chamber is prepared separately and fuels are burned in a small combustion chamber. After heating to the temperature of 700° C. or above, preferably 1000° C. or above, an aqueous solution of an organic compound like an aqueous alcohol solution is sprayed to cause water vapor microexplosion, and as result high-temperature gas is produced and transported to the chamber for
heat treatment 201 to be utilized for power generation or the like. - By using the device illustrated in
FIG. 1 , heavy oil A was sprayed at 5.9 L/H from the first burner 2 (air ratio: 1.5) to pre-heat thecombustion chamber 1. - When the exit temperature of the combustion chamber is about 800° C. as measured by the thermometer T2, 40% by volume aqueous ethanol solution was sprayed at 11 L/H by using the
second burner 3. - After 20 minutes, the thermometer T2 showed 1010° C., indicating temperature increase of 210° C.
- At that time, temperature of the chamber for heat treatment 201 (the thermometer T3) increased by 170° C. from 610° C. to 780° C.
- Meanwhile, when 30% by volume aqueous ethanol solution was used under the same condition, the temperature increase was rather slow, that is, the thermometer T2 showed 980° C., indicating an increase of 180° C. and the thermometer T3 showed 750° C., indicating an increase of 140° C.
- The above results are illustrated in the
FIG. 3 (a graph illustrating the temperature change inside the device). - The reason for above needs to be further clarified. However, it is believed that, according to collision of liquid micro-droplets of an aqueous ethanol solution with a heat resistant reflector which has been heated to 700° C. or above, water vapor microexplosion occurs. The microexplosion exhibits more intense energy as the temperature increases. In particular, ethanol is dissolved in water while sharing clusters with water, and also by having low boiling point of 78.4° C., molecular bonding in ethanol is broken or weakened by intense water vapor microexplosion, and with rapid progress of an aqueous gas reaction and an oxidation reaction, a significant temperature increase is caused.
- Further, in this example, the high-temperature gas within the
pathway 301 and the chamber forheat treatment 201 is high-temperature and superheated steam containing a large amount of water vapor. - Next, another example is explained.
- First, heavy oil A was sprayed at 6.6 L/H (5.7 kg/H) from a
first burner 2 to heat acombustion chamber 1. After heating for about one hour, temperature of a chamber forheat treatment 201 was 630° C. as measured by T3. - When 30% by volume aqueous ethanol solution (ethanol 4.6 L+water 10.6 L) was sprayed at 15.2 L/H by using a
second burner 3, temperature of the chamber forheat treatment 201 as measured by T3 showed an increase of 190° C. from 630° C. to 820° C. - For the comparison, instead of 30% by volume aqueous ethanol solution, the same amount of pure ethanol was added and sprayed at 4.6 L/H by using the
second burner 3, and as a result, temperature of the chamber forheat treatment 201 showed an increase of only 130° C., i.e., from 630° C. to 760° C. - The results are illustrated in
FIG. 4 . - Since the chamber for
heat treatment 201 is used as a heating device for actual industrial use, the temperature increase in the chamber forheat treatment 201 is most critical in terms of thermal efficiency. - Further, when heat calorie is compared between the addition of pure ethanol and addition of 30% by volume aqueous ethanol solution, amount of gas produced by combustion of heavy oil A at 6.6 L/H (5.7 kg/H) was 97 Nm3, which is then changed to 101 Nm3 with addition of 4.6 L of ethanol or 114 Nm3 with addition of 15.2 L of 30% by volume aqueous ethanol solution.
- Specific heat of gases is as follows: CO2 0.54 kcal/m3, H2O (water vapor) 0.46 kcal/m3, O2 0.35 kcal/m3, N2 0.35 kcal/m3. Gas analysis after burning heavy oil is as follows: CO2 8.4%, H2O 8.8%, O2 6.4%, N2 76.4% and the specific heat of gas was 0.376. Gas analysis after burning heavy oil+ethanol is as follows: CO2 11.6%, H2O 13.8%, O2 0.8%, N2 73.7% (when ethanol is added, air was not particularly introduced, and therefore 6.4% of residual O2 was consumed by burning heavy oil, lowering O2 to 0.8%), and specific heat of gas was 0.387. Gas analysis after burning heavy oil+30% by volume aqueous ethanol solution is as follows: CO2 10.3%, H2O 23.8%, O2 0.7%, N2 65.2%, showing higher ratio of H2O and specific heat of gas was increased to 0.396. When heat calorie for the heat treatment is calculated from these numerical values, it was 25580 kcal/H for heavy oil only, 32940 kcal/H for heavy oil+pure ethanol, and 40590 kcal/H for heavy oil+30% by volume aqueous ethanol solution.
- Thus, the heat calorie of the heavy oil+30% by volume aqueous ethanol solution was increased by 23% compared to the heat calorie of heavy oil+pure ethanol in the same amount.
- The results given as a drawing are illustrated in
FIG. 5 . From the results ofFIG. 5 , the energy was 40590 kcal/H when 30% by volume aqueous ethanol solution is added while it was 32940 kcal/H when only pure ethanol is added. Thus, it is understood that the net energy of 7650 kcal/H, which corresponds to the difference between them (40590-32940=7650 kcal/H), is gained. - As it is understood from the explanations of this example and
FIG. 5 , the high-temperature gas (about 900 to 1100° C.) obtained in this example contains a large amount (23.8%) of H2O (water), and it is also high-temperature and superheated steam. - Taken together, according to the invention, a large amount of high-temperature and superheated steam can be produced with a simple means.
- The test was carried out in the same manner as Example 2 for 30% by volume aqueous methanol solution and pure methanol in the same amount.
- The results are illustrated in
FIG. 6 . - By using the device illustrated in
FIG. 1 , heavy oil A was sprayed at 6.6 L/H from afirst burner 2 into acombustion chamber 1 and heated. After heating for 1 hour, a thermometer T2 in the pathway connecting the exit of a combustion chamber reached 800° C. and exhibited an almost stable state. Thus, 30% by volume aqueous methanol solution was sprayed at 15.2 L/H (pure methanol 4.6 L/H and water 10.6 L/H) from asecond burner 3. After 20 minutes, the thermometer T2 in the pathway connecting the exit of a combustion chamber showed 940° C., indicating a temperature increase of 140° C. while a thermometer T3 in a chamber for heat treatment showed a temperature increase of 130° C., i.e., from 630° C. to 760° C. - Meanwhile, for the comparison, pure methanol was sprayed at 4.6 L/H by using the
second burner 3, and as a result, the thermometer T2 in the pathway connecting the exit of a combustion chamber showed a temperature increase of 140° C., i.e., from 800° C. to 940° C., which is the same increase as the 30% by volume aqueous methanol solution. However, the thermometer T3 in the chamber for heat treatment increased from 630° C. to 720° C. only. - In this regard, since the utilization of heat in a boiler for power generation or an incinerator is determined by the temperature and flow amount (heat flow amount) of a chamber for heat treatment, it is found by calculation that the heat calorie in a chamber for heat treatment is increased by about 19% in the case in which 30% by volume aqueous methanol solution is added compared to the case in which pure methanol is added in the same amount.
-
FIG. 7 illustrates such results. - From the results illustrated in
FIG. 7 , it is understood that energy was 37,620 kcal/H when 30% by volume aqueous methanol solution is added and the net energy of 5,980 kcal/H, which corresponds to the difference between them (i.e., 37,620-31,640=5,980 kcal), is gained. - As illustrated in the above, 23% heat calorie increase was obtained from the 30% by volume aqueous ethanol solution (Example 2). The heat calorie increase was only 19% for the 30% by volume aqueous methanol solution (Example 3). However, it is believed to have equal to or more than 20% heat calorie increase when the test is carried out under an optimum condition.
- Also in this example, the high-temperature gas within the
pathway 301 and the chamber forheat treatment 201 was high-temperature and superheated steam containing a large amount of high-temperature water vapor. - With the device of in
FIG. 1 , heavy oil was first sprayed at 6.6 L/H and the combustion chamber was heated. - A thermometer T1 measures the temperature at the center of the combustion chamber, a thermometer T2 measures the temperature at the exit of the combustion chamber, and a thermometer T3 measures the temperature around the exit of the chamber for heat treatment. Since the chamber for heat treatment is a place for multipurpose use, it is expected to be used for power generation, or as a boiler or an incinerator or the like. Thus, the thermal efficiency will be improved more as the temperature of the thermometer T3 increases.
- After heating with heavy oil at 6.6 L/H, 30% by volume aqueous methanol solution was sprayed at 21 L/H.
- As a result, the thermometer T2 showed a temperature increase of 120° C., i.e., from 960° C. to 1080° C. and the thermometer T3 showed a temperature increase of 100° C., i.e., from 800° C. to 900° C. The results are as illustrated in
FIG. 8 . - In this example, the same device (
FIG. 1 ) as Example 1 was used. As pre-heating of a combustion chamber, heavy oil A was used at 6.6 L/H and the pre-heating time was 30 minutes. When the temperature of thermometers T2 and T3 is almost stabilized, 30% by volume aqueous methanol solution was sprayed at 25 L/H. - As a result, the thermometer T2 showed a temperature increase of 135° C., i.e., from 965° C. to 1100° C. and the thermometer T3 showed a temperature increase of 130° C., i.e., from 810° C. to 940° C. Since the spray amount of 30% by volume aqueous methanol solution was different between Example 4 and Example 5, i.e., 21 L/H and 25 L/H, respectively, the temperature increase measured by the thermometer T3 was also different, i.e., Example 4: 900° C. (+100° C.) and Example 5: 940° C. (+130° C.). The results are as illustrated in
FIG. 9 . - With the device illustrated in
FIG. 1 , heavy oil A was sprayed at 6.6 L/H from afirst burner 2 to heat the inside of acombustion chamber 1 to 700° C. or above, and then 30% by volume aqueous ethanol solution was sprayed at 15.2 L/H from a second burner 3 (ethanol 4.6 L+water 106 L). - As a result, the thermometer T2 showed a rapid temperature increase of 220° C., i.e., from 780° C. to 1000° C. and the thermometer T3 showed a temperature increase of 190° C., i.e., from 630° C. to 820° C. Eight minutes later, heavy oil A was reduced by 23%, i.e., from 6.6 to 5.1 L/H, and as a result, the thermometer T2 was recovered to the level before the addition of ethanol. Meanwhile, although the thermometer T3 also showed a decrease of 70° C., indicating the temperature of 730° C., but it is still 110° C. higher than the level before the addition of ethanol. The results are as illustrated in
FIG. 10 . - The test was carried out under the same condition as Example 6 to determine the reproducibility. First, to heat a combustion chamber to 700° C. or above, heavy oil A was sprayed at 6.6 L/H from a
first burner 1 to increase the temperature of the combustion chamber. - About forty minutes later, the thermometer T2 and the thermometer T3 showed 800° C. and 640° C., respectively. At that time, 30% by volume aqueous ethanol solution was sprayed at 15.2 L/H.
- As a result, the thermometer T2 showed 980° C., representing a temperature increase of 180° C. and the thermometer T3 showed 800° C., representing a temperature increase of 160° C.
- Twenty minutes later, heavy oil A of the pilot was decreased by 22%, i.e., from 6.6 L/H to 5.1 L/H.
- As a result, the thermometer T2 at the exit of the combustion chamber showed a temperature decrease of 160° C., i.e., from 980° C. to 820° C. and the thermometer T3 at the exit of the chamber for heat treatment showed a temperature decrease of only 70° C., i.e., from 800° C. to 730° C. (however, there is still a difference of 90° C. compared to the temperature of 640° C. obtained originally from heavy oil A only). The results are as illustrated in
FIG. 11 . - Since the heat utilization according to this type is determined by heat calorie of a chamber for heat treatment, the amount of heavy oil A may be further reduced by 22%, thus it is believed that overall 44% reduction can be achieved.
- Addition amount of 30% by volume aqueous methanol solution was changed in this test.
- Specifically, it was added in an amount of 10.6 L/H in Example 8, compared to 21 L/H and 25 L/H in Example 4 and Example 5, respectively.
- As a result, the thermometer T2 showed a temperature increase of 135° C., i.e., from 800° C. to 935° C. and the thermometer T3 showed a temperature increase of only 125° C., i.e., from 625° C. to 745° C. in this example.
- After that, heavy oil A was decreased by 17%, i.e., from 6.6 L/H to 5.5 L/H. However, the temperature of the thermometer T3, which determines the available heat calorie, was decreased to 695° C., showing a decrease of 55° C. Still, there is a difference of 70° C. compared to the temperature of 625° C. obtained originally from heavy oil A at 6.6 L/H. The results are as illustrated in
FIG. 12 . - Based on the results, the amount of heavy oil A may be further reduced by 17%, thus it is believed that overall 34% reduction can be achieved.
- In this example, test was carried out by adding methanol-based waste water (i.e., waste water containing 40% by volume of methanol and slight amount of others like amine and formalin).
- First, heavy oil A was sprayed at 5.7 L/H from a
first burner 2 into acombustion chamber 1 and burned therein followed by heating for about 70 minutes. - When the thermometer T1 of the combustion chamber shows 1050° C. and the thermometer T2 at the exit of the combustion chamber shows 750° C., the methanol-based waste water was added and burned at 11.4 L/H with a
second burner 3. As a result, ten minutes later, the temperature was increased by about 200° C. Thirty minutes after spraying the waste water, the thermometer T2 showed an increase of 230° C., i.e., from 750° C. to 980° C. The results are as illustrated inFIG. 13 . - Further, the temperature of a chamber for heat treatment, which can be used as a thermal engine, showed an increase of 160° C., i.e., from 600° C. to 760° C. Thus, it was confirmed that the methanol-based organic waste water can be used for the invention.
- Conventionally, as a waste, waste water containing methanol in an amount of 40% by volume or so is handed over to a waste water management company with charge since the waste water is not burned as it is. However, according to the invention, it may be fully utilized as a fuel and also a cost required for handing over to a waste management company can be saved.
- In Examples 4 to 9, the high-temperature gas within the
pathway 301 and the chamber forheat treatment 201 was also high-temperature and superheated steam containing a large amount of water vapor.
Claims (19)
1. A high-temperature combustion method using fuels and an aqueous solution of an organic compound, comprising: in a combustion chamber,
(1) spraying and burning a fuel with a first burner to heat the interior temperature of a combustion chamber to a high temperature of 700° C. or above; and
(2) spraying subsequently an aqueous solution of an organic compound with a second burner into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature.
2. A high-temperature combustion method using fuels and an aqueous solution of an organic compound, comprising:
(1) spraying and burning in a combustion chamber a fuel with a first burner to heat the interior temperature of the combustion chamber to a high temperature of 700° C. or above;
(2) spraying subsequently in the combustion chamber an aqueous solution of an organic compound with a second burner into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature; and
(3) burning completely in a chamber for heat treatment, which is installed to be connected to the combustion chamber, the combustion gas introduced from the combustion chamber for elevating the temperature to a high temperature.
3. The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to claim 1 , comprising:
(1) spraying and burning in a combustion chamber a fuel with a first burner to heat a heat resistant reflector installed within the combustion chamber to 700° C. or above; and
(2) spraying subsequently in the combustion chamber an aqueous solution of an organic compound with a second burner into high-temperature combustion gas obtained with the first burner followed by mixing and burning, and further elevating the interior temperature to higher temperature by colliding with the surface of the heat resistant reflector being heated.
4. The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to claim 3 , wherein the heat resistant reflector is a metal or ceramic reflector including several holes.
5. The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to claim 1 , wherein the organic compound of the aqueous solution of an organic compound has boiling point of 100° C. or less and is soluble in water.
6. The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to claim 1 , wherein the organic compound of the aqueous solution of an organic compound is one or more types that are selected from water-soluble alcohols, organic acids, aldehydes, and ketones.
7. The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to claim 1 , wherein the aqueous solution of an organic compound is an aqueous alcohol solution comprising 10 to 50% by volume of ethanol or methanol.
8. The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to claim 1 , wherein the fuel sprayed with the first burner is any one or more types that are selected from petroleum oils like kerosene oil and light oil, organic solvents like alcohols, city gas, LPG, natural gas, hydrogen gas, and brown gas.
9. The high-temperature combustion method using fuels and an aqueous solution of an organic compound according to claim 1 , wherein the aqueous solution of an organic compound comprises hardly-decomposable toxic materials including a benzene ring as a skeleton structure like dioxin and PCB and the benzene ring of the toxic materials are detoxified by decomposition in a combustion chamber.
10. A method of producing high-temperature and superheated steam by using the method described in claim 1 .
11. A device for high-temperature combustion using fuels and an aqueous solution of an organic compound, comprising
(1) a combustion chamber,
(2) a first burner attached thereto to spray and burn a fuel in the inside of the combustion chamber so that the interior temperature of the combustion chamber is heated to a high temperature of 700° C. or above, and
(3) a second burner which is attached close to the first burner and used for spraying an aqueous solution of an organic compound into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature.
12. A device for high-temperature combustion using fuels and an aqueous solution of an organic compound, comprising
(1) a combustion chamber,
(2) a first burner attached thereto to spray and burn a fuel in the inside of the combustion chamber so that the interior temperature of the combustion chamber is heated to a high temperature of 700° C. or above,
(3) a second burner which is attached close to the first burner and used for spraying an aqueous solution of an organic compound into high-temperature combustion gas obtained with the first burner followed by mixing and burning for further elevating the interior temperature to higher temperature, and
(4) a chamber for heat treatment which is installed to be connected to the combustion chamber.
13. The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to claim 11 , wherein a means for connecting the combustion chamber and the chamber for heat treatment is a pathway with reduced diameter, which is installed between an exit of the combustion chamber and an entrance of the chamber for heat treatment.
14. The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to claim 11 , wherein a heat resistant reflector is disposed and installed in the combustion chamber.
15. The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to claim 13 , wherein the heat resistant reflector is a metal or ceramic reflector including several holes.
16. The method for high-temperature combustion using fuels and an aqueous solution of an organic compound according to claim 10 , wherein the organic compound of the aqueous solution of an organic compound has boiling point of 100° C. or less and is soluble in water.
17. The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to claim 10 , wherein the aqueous solution of an organic compound sprayed with the second burner is an aqueous alcohol solution comprising 10 to 50% by volume of ethanol or methanol.
18. The device for high-temperature combustion using fuels and an aqueous solution of an organic compound according to claim 10 , wherein the fuel sprayed with the first burner is any one or more types that are selected from petroleum oils like kerosene oil and light oil, organic solvents like alcohols, city gas, LPG, natural gas, hydrogen gas, and brown gas.
19. A device for producing superheated steam using the device described in claim 11 .
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010-002281 | 2010-01-07 | ||
| JP2010002281 | 2010-01-07 | ||
| PCT/JP2011/050606 WO2011083877A1 (en) | 2010-01-07 | 2011-01-07 | Method and device for high-temperature combustion using fuel and aqueous solution of organic compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20120308941A1 true US20120308941A1 (en) | 2012-12-06 |
Family
ID=44305611
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/520,690 Abandoned US20120308941A1 (en) | 2010-01-07 | 2011-01-07 | Method and device for high-temperature combustion using fuel and aqueous solution of organic compound |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20120308941A1 (en) |
| JP (1) | JPWO2011083877A1 (en) |
| CN (1) | CN102893087B (en) |
| WO (1) | WO2011083877A1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5006467B1 (en) * | 2011-12-02 | 2012-08-22 | 吉田工業株式会社 | Dioxin incineration treatment apparatus and method |
| CN103900098B (en) * | 2012-12-26 | 2016-03-30 | 陈彦佐 | Hydrogen energy waste heat boiler combustion-supporting system |
| CN106318485B (en) * | 2016-08-17 | 2018-08-21 | 李广信 | A kind of bio oil and using the bio oil as the burning process of fuel |
| CN107694275B (en) * | 2017-10-16 | 2024-02-20 | 杭州华申元环保科技有限公司 | VOCS waste gas treatment method and device |
| CN108844081B (en) * | 2018-06-29 | 2020-01-10 | 赣州东绿环保科技有限公司 | High-concentration organic sewage incineration purification system and method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001116235A (en) * | 1999-10-15 | 2001-04-27 | Asahi Eng Co Ltd | Waste liquid-incinerating device |
| US6592361B2 (en) * | 2000-05-17 | 2003-07-15 | Kayyani C. Adiga | Process for pre-heating a hydro-fuel and producing in-situ steam for cooking |
| JP2008261534A (en) * | 2007-04-11 | 2008-10-30 | Nihonkai Shoji:Kk | Steam boiler and hot water boiler using emulsion fuel, and combustion method of emulsion fuel |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4849272A (en) * | 1971-10-26 | 1973-07-11 | ||
| JPS5226777A (en) * | 1975-08-26 | 1977-02-28 | Yoshida Hachiro | Method of starting and stopping waste oil burning device |
| JPS5434566A (en) * | 1977-08-04 | 1979-03-14 | Kojin Kk | Method of incinerating waste liquid |
| JPS6050303A (en) * | 1983-08-29 | 1985-03-20 | Toyo Kenko Kk | Incinerating furnace for oil-water mixture |
| JPH03128235U (en) * | 1990-04-05 | 1991-12-24 | ||
| JPH04283309A (en) * | 1991-03-12 | 1992-10-08 | Kiyomoto Tekko Kk | Method for incinerating waste liquid containing nitrogen compound |
| JP3553409B2 (en) * | 1999-03-31 | 2004-08-11 | 株式会社ナカニシ技研 | Hydrofuel combustion device |
| JP2001173930A (en) * | 1999-12-22 | 2001-06-29 | Mitsubishi Materials Corp | Recovery processing method for effluent oil and apparatus therefor |
| JP2002156107A (en) * | 2000-11-17 | 2002-05-31 | 照美 ▲巻▼木 | Method for incinerating waste by waste oil and incinerator used for the method |
| JP4185289B2 (en) * | 2002-02-08 | 2008-11-26 | 出光興産株式会社 | Waste liquid incineration method and mixed liquid using industrial combustion equipment |
| SG174732A1 (en) * | 2006-09-01 | 2011-10-28 | Nanomizer Inc | Method for production of emulsion fuel and apparatus for production of the fuel |
| JP4996932B2 (en) * | 2007-01-29 | 2012-08-08 | 日本ペイント株式会社 | Solvent combustion treatment equipment |
| JP2009074782A (en) * | 2007-09-19 | 2009-04-09 | Yukio Ishii | Hydration fuel combustion device |
| JP2009074730A (en) * | 2007-09-19 | 2009-04-09 | Sg Engineering Kk | Combustion method and device for emulsion fuel |
| CN201203110Y (en) * | 2008-04-30 | 2009-03-04 | 石井幸雄 | Water feeding fuel combustion apparatus |
-
2011
- 2011-01-07 CN CN201180012845.7A patent/CN102893087B/en not_active Expired - Fee Related
- 2011-01-07 JP JP2011549045A patent/JPWO2011083877A1/en active Pending
- 2011-01-07 WO PCT/JP2011/050606 patent/WO2011083877A1/en active Application Filing
- 2011-01-07 US US13/520,690 patent/US20120308941A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001116235A (en) * | 1999-10-15 | 2001-04-27 | Asahi Eng Co Ltd | Waste liquid-incinerating device |
| US6592361B2 (en) * | 2000-05-17 | 2003-07-15 | Kayyani C. Adiga | Process for pre-heating a hydro-fuel and producing in-situ steam for cooking |
| JP2008261534A (en) * | 2007-04-11 | 2008-10-30 | Nihonkai Shoji:Kk | Steam boiler and hot water boiler using emulsion fuel, and combustion method of emulsion fuel |
Non-Patent Citations (1)
| Title |
|---|
| Conrad, Mike; April 13, 2000; http://www.madsci.org/posts/archives/2000-04/956095844.Ch.r.html * |
Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2011083877A1 (en) | 2013-05-16 |
| CN102893087B (en) | 2015-09-30 |
| CN102893087A (en) | 2013-01-23 |
| WO2011083877A1 (en) | 2011-07-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Martin et al. | Combustion performance of pyrolysis oil/ethanol blends in a residential-scale oil-fired boiler | |
| US20120308941A1 (en) | Method and device for high-temperature combustion using fuel and aqueous solution of organic compound | |
| Sungur et al. | Effects of nanoparticle additives to diesel on the combustion performance and emissions of a flame tube boiler | |
| Khateeb et al. | Influence of asphaltene concentration on the combustion of a heavy fuel oil droplet | |
| Ren et al. | Supercritical water oxidation of quinoline with moderate preheat temperature and initial concentration | |
| JPH11166705A (en) | Method and apparatus for burning water-fossil fuel mixed emulsion | |
| Mishra | Fundamentals of combustion | |
| RU2027036C1 (en) | Method of improving combustion with hydrocarbon compositions | |
| JP5446351B2 (en) | High temperature combustion method and apparatus using fuel and organic compound aqueous solution | |
| Shi et al. | A novel combustion system for liquid fuel evaporating and burning | |
| Larionov et al. | Energy recycling of pyrolysis water as a part of coal‐water fuel | |
| Yontar et al. | Combustion characteristics of trimethyl borate, diesel, and trimethyl borate-diesel blend droplets | |
| Shehata et al. | Combustion characteristics for turbulent prevaporized premixed flame using commercial light diesel and kerosene fuels | |
| US10082288B2 (en) | Process for high efficiency, low pollution fuel conversion | |
| Xie et al. | Flow field, flame structure and emissions quantifications of oxygenated glycerol in a swirl flame combustor | |
| Kopyev et al. | Combustion of kerosene sprayed with a jet of superheated steam | |
| US10718511B2 (en) | System for combustion of fuel to provide high efficiency, low pollution energy | |
| JPH08270917A (en) | Waste fluid burning apparatus | |
| Lin et al. | Thermochemical conversion characteristics of a single wood pellet in a convective low‐temperature air environment | |
| JP2001296002A (en) | Combustion method using water. | |
| Gvozdyakov et al. | Cocombustion of Coal–Water Fuel with Fuel Oil | |
| Pourhoseini et al. | Cofiring of renewable biodiesel fuels inside natural gas flame for enhancement of thermal properties of flame and NOx reduction | |
| Vershinina et al. | Combustion of coal flotation wastes and woodworking wastes in blends and suspensions | |
| Antonov et al. | A Comparison of Characteristics of Two-Liquid Droplets Fragmentation with a Variable Volatile Component | |
| JP2005533158A (en) | Liquid hydrocarbon combustion method |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF Free format text: CONFIRMATORY LICENSE;ASSIGNOR:HARVARD UNIVERSITY;REEL/FRAME:028783/0684 Effective date: 20120727 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |