US2800172A - Additives to fuel - Google Patents

Additives to fuel Download PDF

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Publication number
US2800172A
US2800172A US247334A US24733451A US2800172A US 2800172 A US2800172 A US 2800172A US 247334 A US247334 A US 247334A US 24733451 A US24733451 A US 24733451A US 2800172 A US2800172 A US 2800172A
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fuel oil
fuel
additive
slurry
tank
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US247334A
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John B Romer
James H Phillips
Lambert F Kooistra
Frederic G Ely
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Babcock and Wilcox Co
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Babcock and Wilcox Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/12Inorganic compounds
    • C10L1/1233Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/188Carboxylic acids; metal salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/188Carboxylic acids; metal salts thereof
    • C10L1/1888Carboxylic acids; metal salts thereof tall oil

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Incineration Of Waste (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)

Description

July 23, "l 957 J. B. ROMER ET AL ADDITIVES TO FUEL Filed Sept. 19, 1951 MG TOR Jo/m 5 Rome! James 7. Phillips Lambert ZJfiloz'sfra Frederic 5 fly INVENTORS ATTORNEY United States atent Ofiice 2,800,172 Patented July 23, 1957 ADDITIVES T FUEL John B. Romer, Akron, James H. Phillips, Alliance, Lambert F. Kooistra, Akron, and Frederic G. Ely, Paris, Ohio, assignors to The Babcock & Wilcox Company, Rockleigh, N. 3., a corporation ofNeW Jersey Application September 19, 1951, Serial No. 247,334
2 Claims. (Cl. 158-1) The present invention relates to the suspension burning of ash-bearing fuels, and more particularly to the combustion of ash-bearing fuels in connection with the heating of tubular heat absorbing apparatus whereby the character of rash accumulation on the heat absorbing apparatus is modified by the addition of metal base materials.
When gaseous, liquid, or fine solid fuels are burned in suspension in the air supplied for combustion purposes the large proportion, if not the major portion, of the noncombustible constituents of the fuel are carried out of the furnace with the products of combustion. Efiicient combustion of any of these fuels results in high temperatures, above the ash fusion temperature of at least the majority of the non-combustible ash constituents, so that suspended ash particles existing in the products of combustion will remain some time in a molten condition. While some cooling of the gaseous products of combustion and the suspended ash particles may result from furnace Wall cooling, the ash particles are frequently at or above the temperature at which they are viscous when they leave the furnace and some attach themselves to tubular heat exchange surfaces extending across the gas stream. When superheaters for relatively high steam temperatures are involved, the metal temperature of the superheater tubes will be considerably higher than the metal temperature of the steam generating tubes. With the customary temperature of gases flowing over the superheater tubes a condition occurs which is conducive to the accumulation of slag or fused ash on such superheater tubes.
The accumulation of ash or slag on the heat exchange surfaces reduces the heat absorbing ability thereof and continued accumulation of slag will tend to build across the intertube spaces so as to increase the gas flow resistance, resulting in a reduction in the vapor generating and superheating capacity of the unit. While it has been the customary practice to periodically remove or reduce slag accumulations on the tubes by means of steam or water lances, or air blowers, it has been found in the suspension burning of some fuels the slag accumulation on the tubes is of such a tenacious character that the customary methods of slag removal are inadequate.
The quality of the liquid petroleum fuels burned in central station vapor generating plants has deteriorated during the past decade, particularly with regard to the amount and composition of the non-combustible constituents of the fuel. This not only results in an increasing amount of slag, but the nature of such slag has also changed so as to form hard rock-like deposits on the heat absorbing surfaces of the vapor generator. Apparently the slag is hardest and most ditficult to remove by mechanical means when it has accumulated on relatively high temperature heat transfer surfaces, such as .on the superheater tubes when a convection type steam superheater is arranged to deliver the steam at a temperature of the order of 800- 1000 R, or higher. Samples of the hard, closely packed layers of slag deposited on the superheater tubes of generator units which have encountered slag ditficulties have shown high vanadium and/ or sodium sulfate contents. While such slags are somewhat corrosive in contact with the tubes the principal difficulty caused by the slag accumulations has been the reduction in the heat transfer rate to the fluid confined by the tubes. Tube metal corrosion can occur by reason of these slag deposits with the seriousness of the corrosion problem increasing with increases in tube temperatures which promotes the formation of corrosive materials in contact with the tubes.
In the present invention metallic oxides having a relatively high melting temperature are combined with the slag forming constituents of the ash-bearing fuel to dilute and thereby modify the character of the slag whenever deposits are formed on the heat transfer surfaces of a vapor generating and superheating unit. This change in the character of the deposits is evidenced in that the physical nature is such that it is softer and more friable. While some chemical reactions between the residual elements from the fuel and the additives undoubtedly occur, the change as regards the deposits is considered to be primarily due to their dilutent action in providing a matrix which makes the deposit more friable. With the use of additives it has become possible to maintain heat exchange surfaces clean over extended periods of operation without substantial loss of heat transfer efficiency, and with a minimum expenditure of slag removal labor costs.
In general this invention can be used in the suspension burning of ash-bearing fuel where it is desirable to increase the average fusion temperature of the non-combustible residue resulting from the combustion of the fuel. The invention is particularly advantageous in the burning of liquid petroleum fuels which form slags having high vanadium compounds and/ or sodium sulfate contents.
According to the present invention the additive material is introduced into the combustion Zone of the furnace so that finely divided high fusion temperature residual particles are dispersed through the gaseous products of combustion of the fuel and will be carried in suspension therein. More specifically the additive particlesconsist substantially of metallic oxides having fusion temperatures in excess of 2500 F. The additives may be introduced into the furnace in solution or suspension in the fuel; entrained with the combustion air; or injected separately at some other location in the furnace or boiler unit. This mixing of the additive materialwith the noncombustible ash constituents of the fuel is necessary for adequate dilution of the slag deposits. When using a liquid petroleum fuel, we prefer to mix the additive with the fuel prior to its combustion.
The additive may be metallic, aluminum or magnesium, which will be converted to the oxide under the combustion conditions in the furnace. Alternately, the additives may be in the form of an oxide of a metal such as for example MgO or CaO. When the additives are inthe metallic oxide form, they can be a fine powder which may be mixed with the fuel or introduced for entrainment with the combustion air. As a further alternative, the additives may be in the form of an organic or inorganic compound of one of the metals aluminum, calcium or magnesium or as a natural or artificial combination of two or more of these metals, such as for example, salts of carboxylic acids or phenolic compounds or as metallic carbonates or hydrates.
Regardless of the original form of the additive, the non-combustible residues thereof must be in a non-reactive or inert form, i. e. substantially all of the oxides should be of aluminum, magnesium and/ or calcium, with a minimized deposit of other metallic oxides, such' as, for example, iron oxides and/ or vanadium oxides, which have a catalytic effect as regards the formation of sulphur trioxide and sodium-sulphur compounds under combustion temperature conditions.
In selecting an additive for use in any particular unit they should advantageously be of alow unit cost to,
minimize increases in the operating expenses of the heat exchange unit, However, in power generating units, Where additives are used, the resulting ability to maintain clean heating surfaces over long periods of operation: with low labor costs resulting from the changed characteristics' of the slag deposits, will justify a reasonable additive expense.
As a general rule the amount of additive used is controlled so that the metal oxide slag dilutent is approximately proportional to the weightof ash in the liquid;
fuel. This proportion will change with circumstances; as for example when a'vaporgenerating unit is operated with arelatively high superheated steam temperature, the,
ratio of additive weight to fuel ashweight may require:
the. formation of as much as two pounds of metal oxide" for each pound of ash in the fuel. On theother-hand, the ratio of additive weight to ashweight may be less thanone when lower design superheat temperatures are involved in the vapor generator. The composition of the fuel ash will also influence the amount of additive material used.
By way of example, but not of limitation, asteam generating and superheating unit having a capacity of 300,000 pounds of steam per hour and asuperheated steam temperature of 910 F. was fired with commercial fuel oil over extended periods of time, both with and without the use of a fuel additive. The fuel burned was No. 6 fuel oil ASTM designation D39648T, with an average analysis of 3.0% sulphur and .12% ash, and having combustible constituents in excess of 99.0%.
When operating the unit without a fuel additive, the unit was removed from service twice each year for cleaning. A month or six weeks after each cleaning outage, it became necessary to lance the superheater with boiler. water and to air lance and water wash the air heater. In addition, normal soot blower practice including automatic blowers in the superheater cavity between the wide and close spaced superheater tube banks, was continued.
An additive of the type described, in an amount substantially equal in weight to the ash content of the fuel, was used for extended operating periods for comparative purposes. Additives having a fineness of approximately 98% through the-325 mesh screen were mixed with the fuel oil prior to theintroductionof the mixture into the furnace, through an atomizing burner.
The drawing illustrates aschematic arrangement of apparatus for carrying out the method of the present invention.
As shown, a vapor generator 10' of known type, as shown in detail by U. S. Patent No. 2,561,875, is fired by liquid petroleum fuel through the burners 11. The burners are positioned in a wall of the vapor generator to receive fuel under pressure from storage 12 through a supply conduit 13. A slurry of the liquid fuel and additive material is prepared in associated equipment which is connected with the conduit 13 for the removal of fuel therefrom and the introduction thereto of the slurry.
The arrangement of'equipment for preparing a slurry of fuel oil and additive material, and mixing the slurry with the fuel oil delivered to the burners is illustrated in the drawing. As. shown, the equipment includes a tank 14 having a usable capacity of approximately 250 gal. of slurry. The tank is provided with an external layer of heat insulatingmaterial, and is furtherprovided with a motor driven agitator 16 to maintain the additive in liquid suspension while in the mixing tank. A motor driven slurry pump 17 is located externally of the mixing tank. The. pump is arranged for variable speed operation and is interconnected, with the tank 14 and the burner fuel line 13 for the delivery of controlled amounts of additive containing slurry to the fuel burners 11.
Fuel oil for batch mixing with the additive is supplied through a valved pipe 20, while the slurry is withdrawn from the tank 14 through a pipe 21 leading to the inlet of the proportioning pump 17. The slurry discharge from the pump passes through a pipe 22 to a mixing T 23 where it mixes with the fuel oil moving through a stub connection 24 from the main fuel oil supply pipe 13. Leaving the T 23, the mixture of oil and slurry passes through a pipe 25 to the main supply pipe 13' and thence through a pressure regulating and How metering station 26 to the burners 11. The pump 17 is of the flooded suction type, with a small sized tubular connection 27 leading from the pipe 20 tothe pump and thence to the tank 14. A pressure relief valve 28 and connecting piping 30 between the discharge and inlet pipe connection i provided from and to the pump. Advantageously a by-pass pipe 31 and valve 32 connects the main supply pipe 13 section between the pipes 24 and 25, so thatwhen necessary the additive supply to the burner can be discontinued without interruption of the fuel supply to the burners.
The use of the additive changed the characteristic of theslag deposits on the superheater tubes so that it was unnecessary to water wash or water lance the tube banks inorder to remove some of the slag deposit. The customary use of steam soot blowing equipment was; discontinued and it was found that adequate cleaningof the tube surfaces could be attained by air lancing with an air pressure of 225 p; s. i. The air lancing was done once a week and the unit wasmaintained in service with permissible reduction inheat transfer efliciency throughout the normal operating periodof 6 months beween shutdowns. The use of additives sometimes results in an increase in the rate of slag accumulation on the water tube walls of the furnace, but this .slag can also be easily removed by the use. of an air lance, when deemed desirable.
A comparison of the chemical analysis of the two deposits with and without alumina as the additive is tabulated below.
Chemical Analysis Prior to Additives With Additives Percent Percent 2. 8 1.1 2. 1 53; 7 0. l 0. 1 l. 8 3. 2 l. 4 0.3 0. 037 0. 06 Nil Nil 7. 8 2: 4 1.8 1.0 43. 8 18; 6 8. 6 6. 6 2. -9 1. 3 81 6 1. 2 18. 6 8. 4 0. 2 0. 4 Nil 1. 7
Fusion Temperatures Red l Oxid 2 Red Oxid Initial Def 2, 260 l, 640 2, 900+ 2, 900+ Soft Temp 2, 380 2, 660 2, 900+ 2, 900+ Fluid Temp; 2, 460 2, 900+ 2, 900+ 2, 900-!- 1 Shrinkage and drainage began at'1750 I and continued through run; 2 Shrinlrageand drainage began at approximately 2050 It will be noted that theaddition of the additive to the petroleumfuelv increased the A1203 content of the slag deposit to a value approximating 50% of the total,
ing petroleum fuel oil which comprises walls defining a combustion chamber; a source of petroleum fuel oil; means connecting said source and said combustion chamher for fuel oil flow to the latter; tank means; means of the additive was granular, soft and powdery in ap- V pearance. While in accordance with the provisions of the statutes we have illustrated and described herein a preferred embodiment of the invention, those skilled in the art will understand that changes may be made in the method of operation and form of the apparatus disclosed without departing from the spirit of the invention covered by our claims, and that certain features of the invention may sometimes be used to advantage without a corresponding use of other features.
We claim:
1. The method of burning an ash-bearing petroleum fuel oil in a combustion zone which comprises supplying a stream of said petroleum fuel oil to said combustion zone; withdrawing a small quantity of said fuel oil from the stream passing to said combustion zone; mixing said withdrawn fuel oil and a finely divided additive to form a slurry wherein said additive consists of a metal compound containing at least one of the metals aluminum, magnesium and calcium; mechanically agitating said slurry to maintain saidfinely divided additive in oil suspension; and adding a controlled quantity of said slurry to the fuel oil stream delivered to said combustion zone, said slurry being added at a rate suflicient to provide and additive weight addition to the fuel oil delivered to said combustion zone substantially equal to the weight of natural ash in the fuel oil.
2. Apparatus for preparing and burning an ash-bearfor withdrawing a small quantity of said fuel oil from said connecting means and discharging the oil to said tank means; means for introducing a finely divided additive to said tank to form a slurry wherein said additive consists of ametal compound containing at least one of the metals aluminum, magnesium and calcium; means for mechanically agitating said slurry to maintain said finely divided additive in oil suspension; a pipe connecting said tank to said fuel oil flow means for adding a controlled stream of said slurry to the fuel oil delivered to'said combustion chamber; and proportioning pump means arranged to deliver said slurry to said fuel flow means from said tank at a rate sulficient to provide an additive weight additionto the fuel oil delivered to said combustion chamber substantially equal to the weight of natural ash in the fuel oil.
References Cited in the file of this patent UNITED STATES PATENTS

Claims (1)

  1. 2. APPARATUS FOR PREPARING AND BURNING AN ASH-BEARING PETROLEUM FUEL OIL WHICH COMPRISES WALLS DEFINING A COMBUSTION CHAMBER; A SOURCE OF PETROLEUM FUEL OIL; MEANS CONNECTING SAID SOURCE AND SAID COMBUSTION CHAMBER FOR FUEL OIL FLOW TO THE LATTER; TANK MEANS; MEANS FOR WITHDRAWING A SMALL QUANTITY OF SAID FUEL OIL FROM SAID CONNECTING MEANS AND DISCHARGING THE OIL TO SAID TANK MEANS; MEANS FOR INTRODUCING A FINELY DIVIDED ADDITIVE TO SAID TANK TO FORM A SLURRY WHEREIN SAID ADDITIVE CONSISTS OF A METAL COMPOUND CONTAINING AT LEAST ONE OF THE METALS ALUMINUM, MAGNESIUM AND CALCIUM; MEANS FOR MECHANICALLY AGITATING SAID SLURRY TO MAINTAIN SAID FINELY DIVIDED ADDITIVE IN OIL SUSPENSION; A PIPE CONNECTING SAID TANK TO SAID FUEL OIL FLOW MEANS FOR ADDING A CONTROLLED STREAM OF SAID SLURRY TO THE FUEL OIL DELIVERED TO SAID COMBUSTION CHAMBER; AND PROPORTIONING PUMP MEANS ARRANGED TO DELIVER SAID SLURRY TO SAID FUEL FLOW MEANS FROM SAID TANK AT A RATE SUFFICIENT TO PROVIDE AN ADDITIVE WEIGHT ADDITION TO THE FUEL OIL DELIVERED TO SAID COMBUSTION CHAMBER SUBSTANTIALLY EQUAL TO THE WEIGHT OF NATURAL ASH IN THE FUEL OIL.
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Cited By (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2938782A (en) * 1956-04-24 1960-05-31 Commw Engineering Corp Method and operation of blast furnaces and metallurgical fuels therefor
US2944807A (en) * 1956-11-20 1960-07-12 Shell Oil Co Process for supplying heat to a bed of finely divided refractory material
US2986456A (en) * 1954-08-20 1961-05-30 Ohio Commw Eng Co Liquid hydrocarbon fuel containing powdered coal, metal, and catalyst
US3120864A (en) * 1962-03-05 1964-02-11 Christian G Teufel Apparatus for the introduction of a liquid having solid particles into a desired zone
US4173454A (en) * 1977-07-18 1979-11-06 Heins Sidney M Method for removal of sulfur from coal in stoker furnaces
US4232615A (en) * 1979-06-11 1980-11-11 Aluminum Company Of America Coal burning method to reduce particulate and sulfur emissions
US4235585A (en) * 1978-03-03 1980-11-25 Anderson Hans Christian Process and composition for neutralization of acidic combustion products and for boiler cleaning
US4253408A (en) * 1979-08-24 1981-03-03 The United States Of America As Represented By The Secretary Of The Navy Method of protecting incinerator surfaces
US4308808A (en) * 1979-06-11 1982-01-05 Aluminum Company Of America Coal burning method to reduce particulate and sulfur emissions
FR2488678A1 (en) * 1980-08-14 1982-02-19 Rockwell International Corp METHOD AND APPARATUS FOR COMBUSTION TO SIGNIFICANTLY REDUCE THE EMISSION OF NITROGEN COMPOUNDS FORMED DURING COMBUSTION
EP0073231A1 (en) * 1981-03-03 1983-03-09 Rockwell International Corp Combustion method and apparatus therefor.
US4447203A (en) * 1980-11-28 1984-05-08 Hampton William J Flame combustion of carbonaceous fuels
US4461224A (en) * 1981-02-21 1984-07-24 L. & C. Steinmuller Gmbh Method of minimizing the emission of contaminants from flame combustion
US4469033A (en) * 1981-02-21 1984-09-04 L. & C. Steinmuller Gmbh Method of minimizing the emission of contaminants from combustion plants
US4542704A (en) * 1984-12-14 1985-09-24 Aluminum Company Of America Three-stage process for burning fuel containing sulfur to reduce emission of particulates and sulfur-containing gases
US4582005A (en) * 1984-12-13 1986-04-15 Aluminum Company Of America Fuel burning method to reduce sulfur emissions and form non-toxic sulfur compounds
US4807542A (en) * 1987-11-18 1989-02-28 Transalta Resources Corporation Coal additives
US4940010A (en) * 1988-07-22 1990-07-10 Ogden-Martin Systems, Inc. Acid gas control process and apparatus for waste fired incinerators
US4960577A (en) * 1988-02-04 1990-10-02 Acurex Corporation Enhanced sorbent injection combined with natural gas reburning for a sox control for coal fired boilers
US5092254A (en) * 1988-07-22 1992-03-03 Ogden-Martin Systems, Inc. Acid gas control process and apparatus for waste fired incinerators
US5322671A (en) * 1992-02-25 1994-06-21 Blue Planet Technologies Co., L.P. Catalytic vessel
US5387569A (en) * 1992-02-25 1995-02-07 Blue Planet Technologies Co., L.P. Catalytic solution suitable for converting combustion emissions
US5386690A (en) * 1992-02-25 1995-02-07 Blue Planet Technologies Co., L.P. Catalytic system
US5460790A (en) * 1992-02-25 1995-10-24 Blue Planet Technologies Co., L.P. Catalytic vessel for receiving metal catalysts by deposition from the gas phase
US6152972A (en) * 1993-03-29 2000-11-28 Blue Planet Technologies Co., L.P. Gasoline additives for catalytic control of emissions from combustion engines
US20060257799A1 (en) * 2005-05-10 2006-11-16 Enviromental Energy Services, Inc. Processes for operating a utility boiler and methods therefor
US20090178599A1 (en) * 2008-01-15 2009-07-16 Environmental Energy Services, Inc. Process for operating a coal-fired furnace with reduced slag formation
US20110100015A1 (en) * 2009-11-05 2011-05-05 General Electric Company Gas turbine system to inhibit coke formation and methods of use
US9127228B2 (en) 2011-01-14 2015-09-08 Enviornmental Energy Serivces, Inc. Process for operating a furnace with a bituminous coal and method for reducing slag formation therewith

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US1832827A (en) * 1929-12-12 1931-11-17 Texas Co Apparatus for preparing liquid fuels
GB445506A (en) * 1934-08-06 1936-04-14 Bataafsche Petroleum A process for burning oil
US2086775A (en) * 1936-07-13 1937-07-13 Leo Corp Method of operating an internal combustion engine
GB496692A (en) * 1936-07-27 1938-12-05 Bbc Brown Boveri & Cie Improved method of firing oil fired furnaces
US2141848A (en) * 1938-12-27 Soot remover
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US1336285A (en) * 1920-04-06 Htdiocabbon-bukweb
US2141848A (en) * 1938-12-27 Soot remover
US1832827A (en) * 1929-12-12 1931-11-17 Texas Co Apparatus for preparing liquid fuels
GB445506A (en) * 1934-08-06 1936-04-14 Bataafsche Petroleum A process for burning oil
US2086775A (en) * 1936-07-13 1937-07-13 Leo Corp Method of operating an internal combustion engine
GB496692A (en) * 1936-07-27 1938-12-05 Bbc Brown Boveri & Cie Improved method of firing oil fired furnaces
US2230642A (en) * 1938-08-13 1941-02-04 Standard Oil Dev Co Fuel oil
US2412809A (en) * 1944-06-21 1946-12-17 Comb Eng Co Inc Corrosion reduction in heat exchangers
US2460700A (en) * 1947-07-01 1949-02-01 Leo Corp Method of operating an internal-combustion engine
GB669056A (en) * 1948-02-26 1952-03-26 Bataafsche Petroleum Improvements in and relating to fuels for internal combustion engines and to the operation of such engines
US2631929A (en) * 1948-10-21 1953-03-17 Standard Oil Dev Co Stabilizing vanadium containing fuel oils

Cited By (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2986456A (en) * 1954-08-20 1961-05-30 Ohio Commw Eng Co Liquid hydrocarbon fuel containing powdered coal, metal, and catalyst
US2938782A (en) * 1956-04-24 1960-05-31 Commw Engineering Corp Method and operation of blast furnaces and metallurgical fuels therefor
US2944807A (en) * 1956-11-20 1960-07-12 Shell Oil Co Process for supplying heat to a bed of finely divided refractory material
US3120864A (en) * 1962-03-05 1964-02-11 Christian G Teufel Apparatus for the introduction of a liquid having solid particles into a desired zone
US4173454A (en) * 1977-07-18 1979-11-06 Heins Sidney M Method for removal of sulfur from coal in stoker furnaces
US4235585A (en) * 1978-03-03 1980-11-25 Anderson Hans Christian Process and composition for neutralization of acidic combustion products and for boiler cleaning
US4308808A (en) * 1979-06-11 1982-01-05 Aluminum Company Of America Coal burning method to reduce particulate and sulfur emissions
US4232615A (en) * 1979-06-11 1980-11-11 Aluminum Company Of America Coal burning method to reduce particulate and sulfur emissions
US4253408A (en) * 1979-08-24 1981-03-03 The United States Of America As Represented By The Secretary Of The Navy Method of protecting incinerator surfaces
FR2488678A1 (en) * 1980-08-14 1982-02-19 Rockwell International Corp METHOD AND APPARATUS FOR COMBUSTION TO SIGNIFICANTLY REDUCE THE EMISSION OF NITROGEN COMPOUNDS FORMED DURING COMBUSTION
US4427362A (en) 1980-08-14 1984-01-24 Rockwell International Corporation Combustion method
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