US20080044781A1 - Method of solid fuel combustion intensification - Google Patents
Method of solid fuel combustion intensification Download PDFInfo
- Publication number
- US20080044781A1 US20080044781A1 US11/836,921 US83692107A US2008044781A1 US 20080044781 A1 US20080044781 A1 US 20080044781A1 US 83692107 A US83692107 A US 83692107A US 2008044781 A1 US2008044781 A1 US 2008044781A1
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- Prior art keywords
- combustion
- fuel
- oxygen
- zone
- combustion zone
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Links
- 238000002485 combustion reaction Methods 0.000 title claims abstract description 50
- 238000000034 method Methods 0.000 title claims abstract description 30
- 239000004449 solid propellant Substances 0.000 title claims description 11
- 239000000446 fuel Substances 0.000 claims abstract description 15
- 230000004913 activation Effects 0.000 claims abstract description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 9
- 230000005684 electric field Effects 0.000 claims abstract description 9
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 9
- 239000001301 oxygen Substances 0.000 claims abstract description 9
- 239000003054 catalyst Substances 0.000 claims abstract description 8
- 150000003254 radicals Chemical class 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 5
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 3
- 150000001723 carbon free-radicals Chemical class 0.000 claims abstract description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 3
- 230000009467 reduction Effects 0.000 claims abstract description 3
- 239000002184 metal Substances 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 150000002739 metals Chemical class 0.000 claims description 4
- 239000004020 conductor Substances 0.000 claims description 2
- 230000008569 process Effects 0.000 abstract description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052799 carbon Inorganic materials 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract description 5
- 239000003245 coal Substances 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000009434 installation Methods 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000010883 coal ash Substances 0.000 description 1
- 238000010835 comparative analysis Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23B—METHODS OR APPARATUS FOR COMBUSTION USING ONLY SOLID FUEL
- F23B7/00—Combustion techniques; Other solid-fuel combustion apparatus
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23B—METHODS OR APPARATUS FOR COMBUSTION USING ONLY SOLID FUEL
- F23B90/00—Combustion methods not related to a particular type of apparatus
-
- 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
- F23C13/00—Apparatus in which combustion takes place in the presence of catalytic material
-
- 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
- F23C99/00—Subject-matter not provided for in other groups of this subclass
- F23C99/001—Applying electric means or magnetism to combustion
Definitions
- the method relates to the power engineering, metallurgy, and namely, to the solid fuel combustion: coal, peat, wood.
- the method of oxygen-convector steel melting is known (see Kazakov N. F., Osokin A. M., Sishkova A. P. Technology of metals and other structural materials, 1975-688 p.).
- the substance of this method consists in the iron oxygen blow through the lance. During the high-temperature mass oxygen blowing oxidation of hardly oxidized additives is achieved. The highest oxidation of additives takes place at the oxygen jet-metal interface.
- the disadvantages consist in the use of a precious oxidizer, unproductive oxidizer losses due to a large oxygen breakthrough, necessity of obtaining the oxidizer using additional complex and metal consuming technology.
- the disadvantages are that the technology was studied at low concentrations of the reacting components which leads to increase of expenditure of energy for generation of the electric discharge.
- the method of combustion intensification consists in processing the flame with a strong longitudinal electric field (2 kV/cv and more) and a strong transversal electric field rotated, for instance, by means of a three-phase electrode system and a three-phase high-voltage source.
- the method comprises also operation of the flame height measurement and its other parameters, change of the interelectrode distance of the longitudinal field application to the flame with the simultaneous field intensity control.
- the method allows also to rotate the flame by the transversal electric field which increases the mixing and fuel-air reduction degree and additionally enhances the combustion.
- the proposed new operation of electrostatic fuel introduction in the combustion zone by the longitudinal electric field to the molecular level additionally enhances the flame combustion process and decreases fuel consumption.
- the method allows also to control the flame geometry, temperature and heat conduction thereof by the variation of geometry and electric parameters of the above said electric fields, for instance, to focus the flame which is sufficient, for instance, for heat treatment of metals and alloys.
- the disadvantages are high specific power inputs decreasing power efficiency of the process, necessity of fuel mixing and electrostatic atomization, complexity of combustion process regulation.
- the invention is aimed to add to the thermal component of the combustion process activation an electron, wave, light, electrocatalytic activation in order to achieve maximum degree of carbon burning from the solid fuel.
- the essence of the invention is based on the in the fuel-air mixture combustion in the electric field by means of a catalyst located in the combustion zone to which a high voltage is applied, resulting in decrease of activation energies of all endothermic phases of combustion due to creation of oxygen atoms, carbon radicals and oxygen-containing radicals.
- the aim is achieved by overlapping discharge zone, combustion zone and electron-catalytic processes of the synthesis of the low-temperature plasma generated between two electrodes by applying high voltage to the electrodes, the electrodes being made of variable valency metals or their oxides, or other conductive material with the catalyst applied.
- the voltage at the electrodes is within 5 to 20 kV.
- the comparative analysis with the prototype allows making a conclusion that the claimed solution differs from the prototype by the creation of the low-temperature plasma and electrocatalytic processes in the combustion zone.
- the catalytic plasma and oxidation processes are brought in one zone, compared to the prototype the energy expenditures are decreased by three orders, which allows achieving a high specific economy of fuel.
- the fuel expenditures for creation of low-temperature plasma do not exceed 2 to 5% of the energy effect obtained according to the proposed method.
- the method of combustion consists in the following.
- the method by its essence is composed of the physical and thermochemical phases. Fuel grinding, fuel and air transport to the combustion zone, fuel and air mixing and combustion in the combustion chamber of different design are made. Intensification of the combustion process according to the prototype using the electric field relates to the mixing and combustion zone. Intensification of the claimed method relates to the combustion zone where combustion processes, oxidation radical processes, fuel catalytic activation are brought together.
- FIG. 1 installation diagram
- FIG. 2 comparative dependence of the temperature variation of the heat-transfer medium.
- the flowchart of the FIG. 1 comprises: 1 —combustion chamber; 2 —fuel combustion zone; 3 —electrothermal ignition tube of the fuel-air mixture; 4 —reservoir with heated water; 5 —bottom grate; 6 —thermostatic insulation; 7 —high-voltage electrode; 8 —power supply; 9 —ground.
- the air flow containing pulverized solid fuel comes into the combustion chamber 1 . It passes through the grid 7 , bottom grate 5 , and arrives into the zone 2 .
- Electric ignition 3 provides the ignition temperature of the fuel-air mixture and after that it is switched off.
- the stationary combustion process is established which is defined by the heating rate of the precisely measured volume of the heat-transfer medium 4 (water in our case).
- the 5 to 20 kV voltage is supplied from the power supply 8 , 9 to the grid 7 coated with the catalyst enhancing the combustion process. This mode is defined by the heating rate of the equal volume of the heat-transfer medium.
- FIG. 2 shows dependence of the water temperature variation from the time when carrying out idle experiment and with the discharge.
- A zone of establishment of the uniform combustion process (beginning of curves from 0 to 2 minutes);
- B zone of uniform coal combustion: rectilinear section in the middle of the curve, from 2 to 16 minutes; and zone C—extinction of the combustion process (after 16 minutes).
- zone C extinction of the combustion process (after 16 minutes).
- the specific power of heat release in the idle experiment is 73 W/h, while in case of the discharge it averages 94.5 W/h, which is 18.6% higher, and, in its turn, reduces fuel expenditure by the same amount.
- the rate of coal burning was defined. For this purpose, the coal ash and the rate of coal burning with and without the discharge was measured.
- the coal burning rate in the idle experiment is approximately 72% (which approximately corresponds to boilers with the integral grate); the coal burning rate with the use of the discharge amounts to 89%.
- the rate of burning increase was 17.45% on average.
- the proposed method of the combustion process intensification leads to the fuel economy, more complete burning out of the solid fuel and increase of the combustion process efficiency.
- the technical solution claimed allows create an installation for solid fuel combustion intensification for existing boilers of any capacity. Implementation of the technical solution needs not modifications or reworking of the boiler furnaces; electric equipment for creation of electric discharge and low-temperature plasma is standard; catalysts sprayed on the high voltage grid are publicly available.
- the experimental model in the form of the test bed installation is manufactured and tested by the applicants.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
Abstract
Description
- The method relates to the power engineering, metallurgy, and namely, to the solid fuel combustion: coal, peat, wood.
- The process of solid fuel combustion is well known. So far, a considerable number of methods of solid fuel intensification are known. One of the methods consists in combustion intensification by increasing oxygen concentration in the flame, resulting in increasing of atoms and oxygen-containing radicals in the combustion zone.
- The method of oxygen-convector steel melting is known (see Kazakov N. F., Osokin A. M., Sishkova A. P. Technology of metals and other structural materials, 1975-688 p.). The substance of this method consists in the iron oxygen blow through the lance. During the high-temperature mass oxygen blowing oxidation of hardly oxidized additives is achieved. The highest oxidation of additives takes place at the oxygen jet-metal interface.
- The disadvantages consist in the use of a precious oxidizer, unproductive oxidizer losses due to a large oxygen breakthrough, necessity of obtaining the oxidizer using additional complex and metal consuming technology.
- The known from the literature method of intensification of the chemical catalytic heterophase processes by processing catalysis zone with the electric discharge (certificate of authorship No. 1036347, cl. B 01 D35/06/B 01 D 51/00.
- Electrical filter Apr. 30, 1982, and Stolyarenko H. S. Mechanism of chemical radical reactions in heterophase ozone systems H2O—O3—O2—Nox-SO2//Bulletin of Cherkassy engineering-technology institute—
No 3—1999—pp. 81-85). Influence of the electrical discharge on chemical heterophase processes results in the possibility of reactions taking place at temperatures 300 to 500 degrees lower as compared without the influence, which is explained by an additional electron, wave, light activation of process in addition to the temperature activation. - The disadvantages are that the technology was studied at low concentrations of the reacting components which leads to increase of expenditure of energy for generation of the electric discharge.
- “Method of flame intensification and control” (Pat. No. 2125682 Russia, MKI F 23 No. 005/00 F 236005/00) was chosen as a prototype.
- The method of combustion intensification consists in processing the flame with a strong longitudinal electric field (2 kV/cv and more) and a strong transversal electric field rotated, for instance, by means of a three-phase electrode system and a three-phase high-voltage source. The method comprises also operation of the flame height measurement and its other parameters, change of the interelectrode distance of the longitudinal field application to the flame with the simultaneous field intensity control. The method allows also to rotate the flame by the transversal electric field which increases the mixing and fuel-air reduction degree and additionally enhances the combustion. The proposed new operation of electrostatic fuel introduction in the combustion zone by the longitudinal electric field to the molecular level additionally enhances the flame combustion process and decreases fuel consumption. The method allows also to control the flame geometry, temperature and heat conduction thereof by the variation of geometry and electric parameters of the above said electric fields, for instance, to focus the flame which is sufficient, for instance, for heat treatment of metals and alloys.
- The disadvantages are high specific power inputs decreasing power efficiency of the process, necessity of fuel mixing and electrostatic atomization, complexity of combustion process regulation.
- The invention is aimed to add to the thermal component of the combustion process activation an electron, wave, light, electrocatalytic activation in order to achieve maximum degree of carbon burning from the solid fuel.
- The essence of the invention is based on the in the fuel-air mixture combustion in the electric field by means of a catalyst located in the combustion zone to which a high voltage is applied, resulting in decrease of activation energies of all endothermic phases of combustion due to creation of oxygen atoms, carbon radicals and oxygen-containing radicals.
- The aim is achieved by overlapping discharge zone, combustion zone and electron-catalytic processes of the synthesis of the low-temperature plasma generated between two electrodes by applying high voltage to the electrodes, the electrodes being made of variable valency metals or their oxides, or other conductive material with the catalyst applied. The voltage at the electrodes is within 5 to 20 kV.
- The comparative analysis with the prototype allows making a conclusion that the claimed solution differs from the prototype by the creation of the low-temperature plasma and electrocatalytic processes in the combustion zone. This leads to the approach of speeds of thermodestruction and electrocatalytic destruction of carbon and hydrocarbons which are desorbed from the coal; to the increase of the rates of oxidation of the carbon-bearing compounds to the carbon dioxide and water, owing to a high concentration of oxygen-containing radicals, to the increase of the carbon burning degree from the solid fuel and economy of the solid fuel. As the catalytic plasma and oxidation processes are brought in one zone, compared to the prototype the energy expenditures are decreased by three orders, which allows achieving a high specific economy of fuel. The fuel expenditures for creation of low-temperature plasma do not exceed 2 to 5% of the energy effect obtained according to the proposed method.
- The method of combustion consists in the following.
- The method by its essence is composed of the physical and thermochemical phases. Fuel grinding, fuel and air transport to the combustion zone, fuel and air mixing and combustion in the combustion chamber of different design are made. Intensification of the combustion process according to the prototype using the electric field relates to the mixing and combustion zone. Intensification of the claimed method relates to the combustion zone where combustion processes, oxidation radical processes, fuel catalytic activation are brought together.
- The proposed technical solution is explained by the drawings:
- FIG. 1—installation diagram;
- FIG. 2—comparative dependence of the temperature variation of the heat-transfer medium.
- The flowchart of the
FIG. 1 comprises: 1—combustion chamber; 2—fuel combustion zone; 3—electrothermal ignition tube of the fuel-air mixture; 4—reservoir with heated water; 5—bottom grate; 6—thermostatic insulation; 7—high-voltage electrode; 8—power supply; 9—ground. - The air flow containing pulverized solid fuel comes into the
combustion chamber 1. It passes through the grid 7,bottom grate 5, and arrives into thezone 2.Electric ignition 3 provides the ignition temperature of the fuel-air mixture and after that it is switched off. The stationary combustion process is established which is defined by the heating rate of the precisely measured volume of the heat-transfer medium 4 (water in our case). The 5 to 20 kV voltage is supplied from the 8, 9 to the grid 7 coated with the catalyst enhancing the combustion process. This mode is defined by the heating rate of the equal volume of the heat-transfer medium.power supply -
FIG. 2 shows dependence of the water temperature variation from the time when carrying out idle experiment and with the discharge. When coal is combusted with the discharge water heating is accelerated which is evidence of the release of a larger amount of heat as compared to the idle experiment. (On the curves shown three zones can be seen: A—zone of establishment of the uniform combustion process (beginning of curves from 0 to 2 minutes); B—zone of uniform coal combustion: rectilinear section in the middle of the curve, from 2 to 16 minutes; and zone C—extinction of the combustion process (after 16 minutes). For calculations of the coal combustion power and efficiency of the electric activation is used the section of the uniform combustion. - The specific power of heat release in the idle experiment is 73 W/h, while in case of the discharge it averages 94.5 W/h, which is 18.6% higher, and, in its turn, reduces fuel expenditure by the same amount.
- During two experiments the rate of coal burning was defined. For this purpose, the coal ash and the rate of coal burning with and without the discharge was measured. The coal burning rate in the idle experiment is approximately 72% (which approximately corresponds to boilers with the integral grate); the coal burning rate with the use of the discharge amounts to 89%. The rate of burning increase was 17.45% on average.
- When the catalytic grid of the high voltage electrode is removed from the combustion zone, the heat-carrier medium heat rates are approached and the intensification effect of the fuel combustion is decreased and the carbon content in the ash is near the values obtained in the idle experiment.
- Thus, the proposed method of the combustion process intensification leads to the fuel economy, more complete burning out of the solid fuel and increase of the combustion process efficiency.
- The technical solution claimed allows create an installation for solid fuel combustion intensification for existing boilers of any capacity. Implementation of the technical solution needs not modifications or reworking of the boiler furnaces; electric equipment for creation of electric discharge and low-temperature plasma is standard; catalysts sprayed on the high voltage grid are publicly available.
- The experimental model in the form of the test bed installation is manufactured and tested by the applicants.
Claims (3)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| UAA200609123A UA78474C2 (en) | 2006-08-17 | 2006-08-17 | Method for intensification of solid fuel burning |
| UAA200609123 | 2006-08-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20080044781A1 true US20080044781A1 (en) | 2008-02-21 |
Family
ID=37952166
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/836,921 Abandoned US20080044781A1 (en) | 2006-08-17 | 2007-08-10 | Method of solid fuel combustion intensification |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20080044781A1 (en) |
| CN (1) | CN101135439A (en) |
| DE (1) | DE102007038967A1 (en) |
| FR (1) | FR2905001A1 (en) |
| PL (1) | PL383156A1 (en) |
| RU (1) | RU2457395C2 (en) |
| UA (1) | UA78474C2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010074767A1 (en) * | 2008-12-26 | 2010-07-01 | Vacca, Inc. | Jet cavity catalytic heater |
| US20140248566A1 (en) * | 2013-03-04 | 2014-09-04 | Clearsign Combustion Corporation | Combustion system including one or more flame anchoring electrodes and related methods |
| US9618199B2 (en) | 2009-10-22 | 2017-04-11 | Gdf Suez | Radiating burner having enhanced performance and method for improving the performance of a radiating burner |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102517121A (en) * | 2012-01-05 | 2012-06-27 | 江南大学 | Catalysis device for improving combustion calorific value of coal |
| US9289780B2 (en) * | 2012-03-27 | 2016-03-22 | Clearsign Combustion Corporation | Electrically-driven particulate agglomeration in a combustion system |
| WO2013148738A1 (en) * | 2012-03-27 | 2013-10-03 | Clearsign Combustion Corporation | Solid fuel burner with electrodynamic homogenization |
| PL416911A1 (en) | 2016-04-20 | 2017-10-23 | Kmb Catalyst Spółka Z Ograniczoną Odpowiedzialnością | Method of intensification of solid fuels burning process |
| RU2634344C1 (en) * | 2016-08-01 | 2017-10-25 | Акционерное Общество "Сибтехэнерго" - инженерная фирма по наладке, совершенствованию технологий и эксплуатации электро-энергооборудования предприятий и систем | Fuel burning method |
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|---|---|---|---|---|
| US3416780A (en) * | 1966-11-25 | 1968-12-17 | United States Steel Corp | Blast furnace stock line wall and method of constructing the same |
| US3416870A (en) * | 1965-11-01 | 1968-12-17 | Exxon Research Engineering Co | Apparatus for the application of an a.c. electrostatic field to combustion flames |
| US4729821A (en) * | 1986-11-03 | 1988-03-08 | Board Of Regents, The University Of Texas System | In situ activation of catalysts by applied electrical potentials |
| US5458748A (en) * | 1990-07-19 | 1995-10-17 | Thermo Power Corporation | Coronal-catalytic apparatus and method for NOx reduction |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU878774A1 (en) * | 1979-04-10 | 1981-11-07 | Государственный Научно-Исследовательский Энергетический Институт Им.Г.М.Кржижановского | Method of gasifisation of solid carbon-containing fueld |
| FR2491490A1 (en) * | 1980-10-02 | 1982-04-09 | G Energet In | Synthesis gas prodn. from solid fuels - by injecting mixt. of fuel and oxidant into plasma arc |
| FI85910C (en) * | 1989-01-16 | 1992-06-10 | Imatran Voima Oy | FOERFARANDE OCH ANORDNING FOER ATT STARTA PANNAN I ETT KRAFTVERK SOM UTNYTTJAR FAST BRAENSLE SAMT FOER ATT SAEKERSTAELLA FOERBRAENNINGEN AV BRAENSLET. |
| RU2190661C2 (en) * | 2000-07-18 | 2002-10-10 | Государственное унитарное предприятие Научно-производственное объединение "Гидротрубопровод" | Method for reprocessing coal into synthesis gas |
| RU2201554C1 (en) * | 2002-04-10 | 2003-03-27 | Достовалов Виктор Александрович | Method for plasma ignition of pulverized coal |
| BG109247A (en) * | 2005-07-29 | 2005-11-30 | Чавдар АНГЕЛОВ | Method for the conversion of coal into fuels |
-
2006
- 2006-08-17 UA UAA200609123A patent/UA78474C2/en unknown
-
2007
- 2007-08-10 US US11/836,921 patent/US20080044781A1/en not_active Abandoned
- 2007-08-15 RU RU2007131068/06A patent/RU2457395C2/en not_active IP Right Cessation
- 2007-08-16 PL PL383156A patent/PL383156A1/en unknown
- 2007-08-16 CN CNA2007101418927A patent/CN101135439A/en active Pending
- 2007-08-16 FR FR0757074A patent/FR2905001A1/en not_active Withdrawn
- 2007-08-17 DE DE102007038967A patent/DE102007038967A1/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3416870A (en) * | 1965-11-01 | 1968-12-17 | Exxon Research Engineering Co | Apparatus for the application of an a.c. electrostatic field to combustion flames |
| US3416780A (en) * | 1966-11-25 | 1968-12-17 | United States Steel Corp | Blast furnace stock line wall and method of constructing the same |
| US4729821A (en) * | 1986-11-03 | 1988-03-08 | Board Of Regents, The University Of Texas System | In situ activation of catalysts by applied electrical potentials |
| US5458748A (en) * | 1990-07-19 | 1995-10-17 | Thermo Power Corporation | Coronal-catalytic apparatus and method for NOx reduction |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010074767A1 (en) * | 2008-12-26 | 2010-07-01 | Vacca, Inc. | Jet cavity catalytic heater |
| US20100192937A1 (en) * | 2008-12-26 | 2010-08-05 | Vacca, Inc. | Jet Cavity Catalytic Heater |
| JP2012514176A (en) * | 2008-12-26 | 2012-06-21 | ヴァッカ・インコーポレイテッド | Jet cavity catalyst heating device |
| RU2474759C1 (en) * | 2008-12-26 | 2013-02-10 | Гхт Глобал Хитинг Технолоджиз Гмбх | Catalytic heater with spraying cavity |
| US8490617B2 (en) | 2008-12-26 | 2013-07-23 | GHT Global Heating Technologies, GmbH | Jet cavity catalytic heater |
| EP2382419A4 (en) * | 2008-12-26 | 2017-09-27 | GHT Global Heating Technologies GmbH | Jet cavity catalytic heater |
| US9618199B2 (en) | 2009-10-22 | 2017-04-11 | Gdf Suez | Radiating burner having enhanced performance and method for improving the performance of a radiating burner |
| US20140248566A1 (en) * | 2013-03-04 | 2014-09-04 | Clearsign Combustion Corporation | Combustion system including one or more flame anchoring electrodes and related methods |
| US9696034B2 (en) * | 2013-03-04 | 2017-07-04 | Clearsign Combustion Corporation | Combustion system including one or more flame anchoring electrodes and related methods |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2007131068A (en) | 2009-02-20 |
| RU2457395C2 (en) | 2012-07-27 |
| CN101135439A (en) | 2008-03-05 |
| DE102007038967A1 (en) | 2008-02-28 |
| UA78474C2 (en) | 2007-03-15 |
| PL383156A1 (en) | 2008-02-18 |
| FR2905001A1 (en) | 2008-02-22 |
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