US1545620A - Process of producing coke - Google Patents

Process of producing coke Download PDF

Info

Publication number
US1545620A
US1545620A US667046A US66704623A US1545620A US 1545620 A US1545620 A US 1545620A US 667046 A US667046 A US 667046A US 66704623 A US66704623 A US 66704623A US 1545620 A US1545620 A US 1545620A
Authority
US
United States
Prior art keywords
coal
oil
sulphur
limestone
mass
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.)
Expired - Lifetime
Application number
US667046A
Inventor
Trent Walter Edwin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US667046A priority Critical patent/US1545620A/en
Priority to FR586490D priority patent/FR586490A/en
Application granted granted Critical
Publication of US1545620A publication Critical patent/US1545620A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B57/00Other carbonising or coking processes; Features of destructive distillation processes in general
    • C10B57/04Other carbonising or coking processes; Features of destructive distillation processes in general using charges of special composition
    • C10B57/06Other carbonising or coking processes; Features of destructive distillation processes in general using charges of special composition containing additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B57/00Other carbonising or coking processes; Features of destructive distillation processes in general
    • C10B57/08Non-mechanical pretreatment of the charge, e.g. desulfurization
    • 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
    • C10L9/00Treating solid fuels to improve their combustion
    • C10L9/10Treating solid fuels to improve their combustion by using additives

Definitions

  • the invention relates to a process for producing metallurgical coke in which the organic sulphur originally contained in the coal is dissolved in the s a'g when the coke is consumed in a blast furnace.
  • the present invention com by which the most substantia organic sulphur is prevented associated with the iron.
  • very finely ground particles of limestone or lime hydrate or an equivalent substance mixed with Oll are unzformly distributed or mixed with finely ground coal particles forming a plastic mass in which there is a close association between the sulphur and the limestone.
  • tie sulphur of the coal is taken up as calcium sulphide and is dissolved in the slag and discharged from the furnace during a blast furnace operation, thereby preventing deleterious quantities of sulphur from becoming associated with the IIOIl.
  • the invention comprises a process wherein coal is first finely pulverized, and then preferabl saturated with water. Finely pulverize limestone is mixed withhydrocarbon oil, and these substances then commingle with the water saturated or suspended coal particles. The agitation causes the oil, limestone and carbon content of the coal to intimately Application filed October 6, 1923. Serial No. 667,046.
  • the product produced consists of a. plastlc mass in which the fine particles of limestone are uniformly distributed throughout the mass so that the limestone particles are in very close association with the organic sulphur whereby the coking of the mass causes the sulphur to be largely taken up as calcium sulphide. This coking also causes some of the sulphur to be dis charged from the coal as a vapor ,in the form of sulphur gases.
  • I preferably take a bltuminous coal of any des1red grade and reduce this coal bya wet grinding to a fineness suflicient to pass through a screen havlng 1.00 meshes perlinear inch. I then lacethis coal in water suspension or at east wet the coal with water.
  • the oil should be in the proportion of about one-fourth of the coal, or that i's to say, with four tones of coal I preferably use about one ton of oil.
  • the quantity of limestone added maybe from ten'to twelve percent of the oil by weight, although thls will vary considerably, depending upon the sulphur content of coal used and also the type of oil, because many "oils contain a sulphur content, andit is an object to re- 1n the body of oil so as to be uniformly distributed in said oil.
  • the oil with the suspended particles of limestone is then introduced to an agitatingvessel containing the water suspended coal.
  • the oil serving to coat or film the coal and to been coated with oil it has no afiinity carry with it the suspended particles of limestone.
  • Sufficient agitation will cause the oil and coal with the limestone to agglomerate or amalgamate in dense plastic masses of a consistency resembling mortar, or in marble-like agglomerates.
  • Ash forming substances, iron sulphides, etc., originally contained in the coal detached by the fine grinding thereof are excluded from said amalgamated masses together with a greater portion of thewater so that the amalgamated mass consists largely of coal oil, limestone and a small quantity of water.
  • the coal impurities are rejected because having once been saturated in water, they have no aflinity for the oil. It is to be observed, however, that the limestone having once been saturated with the oil and after havinfg once or the water. and therefore remains with the oil and coal while the ash formingsubstances are eliminated.
  • the iron thus produced is not subjected toany substantial quantity of sulphur and for this reason an improved procluct can be obtained.
  • the rocess may be applied to oils that are big in sulphur. for'the purpose of desulphurizing the oil'by first making the oil lime coal mixture then distilling out the oil as gases and condensible vapors.
  • a process of the character described consisting in comm-ingling hydrocarbon oil with finely pulverized coal having a sulphur content to form a substantially plastic mass, and in incorporating with the hydrocarbon oil an agent adapted to be thoroughly distributed throughout the plastic mass of coal and oil to intimately contact with the sulphur content of the coal and possessing the properties of forming with said sulphiu' when the mass is heated calcium sulphide.
  • a purifying proces consisting in intimately mixing finely pulverized'coal containing a sulphur content and a hydrocarform with said sulphur when the mass is subjected to a coking. temperature calcium sulphide.
  • a purifying process which consists in mixing comminuted coal,' hydrocarbon oil and reagent to form a homogeneous mass and to bring said reagent into intimate contact with the sulphur contained in the coal to remove said sulphur when the mass is subjected to acoking temperature.
  • a purifying process which consists in mixing comminuted; coal, hydrocarbon oil and reagent to form a homogeneous mass and to bring said agent into intimate contact with the sulphur contained in the coal to remove said sulphur when the ma& is subjected to a coking temperature as calcium and sulphide compounds.
  • the herein described process consistaceous material. and oxides of the calcium group to form a homogeneous substantially plastic mass.
  • the herein described process consisting in thoroughly mixing a mineral oil with a' wet finely reduced comminuted' mineral carbonaceous material and pulverized oxides of the calcium group.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Combustion & Propulsion (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)

Description

' stantial portion of the organic sulphur never- Patented July 14, 1925.
UNITED STATES PATENT OFFICE.
WALTER EDWIN TRENT, OF WASHINGTON, DISTRICT OF COLUMBIA.
PROCESS OF PRODUCING COKE.
No Drawing.
have invented certain new and useful Improveme'nts in Processes of Producing Coke, of which the following is a specification.
The invention relates to a process for producing metallurgical coke in which the organic sulphur originally contained in the coal is dissolved in the s a'g when the coke is consumed in a blast furnace. I
In the past, efiorts have been made to keep the sulphur out of iron made in blast furnaces by mixing with the coal undergoing a coking treatment, a substance such as limestone. The coarsely ground coal, when mixed with limestone and subjected to a coking action, causes some of the sulphur to combine with the limestone, producing in the coke calcium sulphide, but this reaction is not entlrely satisfactory for. the reason that a very subcomes in contact with the limestone in view of the size of the coal, and therefore a substantial part of the sulphur comes in contact with the pig iron in the blast furnace.
rises a process portion of the from becoming The present invention com by which the most substantia organic sulphur is prevented associated with the iron.- In accordance with this invention very finely ground particles of limestone or lime hydrate or an equivalent substance mixed with Oll, are unzformly distributed or mixed with finely ground coal particles forming a plastic mass in which there is a close association between the sulphur and the limestone. On account of the uniformit of the mixture when the mass is coked tie sulphur of the coal is taken up as calcium sulphide and is dissolved in the slag and discharged from the furnace during a blast furnace operation, thereby preventing deleterious quantities of sulphur from becoming associated with the IIOIl.
In a more specific aspect, the invention comprises a process wherein coal is first finely pulverized, and then preferabl saturated with water. Finely pulverize limestone is mixed withhydrocarbon oil, and these substances then commingle with the water saturated or suspended coal particles. The agitation causes the oil, limestone and carbon content of the coal to intimately Application filed October 6, 1923. Serial No. 667,046.
associate and form a homogeneous plastic mass, excluding water and a substantial portlon of the wet impurities originally contalned in the coal which have no affinity for the oil after once receiving a coating or saturation with water, the specific reaction which occurs having been fully described and broadly claimed in my Patent, No. 1420164 The product produced consists of a. plastlc mass in which the fine particles of limestone are uniformly distributed throughout the mass so that the limestone particles are in very close association with the organic sulphur whereby the coking of the mass causes the sulphur to be largely taken up as calcium sulphide. This coking also causes some of the sulphur to be dis charged from the coal as a vapor ,in the form of sulphur gases. When the coke thus produced is used in a blast furnace the calcium sulphide is absorbed in the slag and dis- 'charged from the furnace, thereby preventing the deleterious sulphur from coming in contact with the pig iron.
In carrying out my process, I preferably take a bltuminous coal of any des1red grade and reduce this coal bya wet grinding to a fineness suflicient to pass through a screen havlng 1.00 meshes perlinear inch. I then lacethis coal in water suspension or at east wet the coal with water. A hydrocarbon oil-which may be fuel oil, gas oil, crude oil or the like, is mixed with limestone which is alsovery finely ground, preferably to the fineness equal to the fineness of the coal. .The oil should be in the proportion of about one-fourth of the coal, or that i's to say, with four tones of coal I preferably use about one ton of oil. The quantity of limestone added maybe from ten'to twelve percent of the oil by weight, although thls will vary considerably, depending upon the sulphur content of coal used and also the type of oil, because many "oils contain a sulphur content, andit is an object to re- 1n the body of oil so as to be uniformly distributed in said oil. The oil with the suspended particles of limestone is then introduced to an agitatingvessel containing the water suspended coal. These substances are at this time mostthoroughly agitated,
the oil serving to coat or film the coal and to been coated with oil, it has no afiinity carry with it the suspended particles of limestone. Sufficient agitation will cause the oil and coal with the limestone to agglomerate or amalgamate in dense plastic masses of a consistency resembling mortar, or in marble-like agglomerates. Ash forming substances, iron sulphides, etc., originally contained in the coal detached by the fine grinding thereof are excluded from said amalgamated masses together with a greater portion of thewater so that the amalgamated mass consists largely of coal oil, limestone and a small quantity of water. The coal impurities are rejected because having once been saturated in water, they have no aflinity for the oil. It is to be observed, however, that the limestone having once been saturated with the oil and after havinfg once or the water. and therefore remains with the oil and coal while the ash formingsubstances are eliminated.
The thorough agitation of these materials, as before stated, results in formation of the amalgamated substances in which the fine particles of lime have been carried by the oil into intimate contact with the coal and becomes uniformly distributed throughout the masses. The lime particles being 1n di rect or intimate contact with the various individual coalparticles, and also with the oil, it is therefore closely associated with the organic sulphur contained in the coal particles and also with the sulphur of the o1 When a mass of the amalgamated material is introduced to the coke oven and subjected to a temperature, some of the organic sul phur leaves as sulphur gases, but the predominating ortion thereof'chemically combines with t e limestone and forms in the coke calcium sulphide. Because of the in timate mixture of-the limestone with the coal and oil, substantially all of this sulphur is caused to unite with the limestone producing calcium sulphide. The coke thus produced when used in a blast furnace in the reduction of iron ores, causes a release of the calcium sulphide which is absorbed in the slag in the furnace, and is discharged therefrom without contact with the pi iron. 7
The iron thus produced, therefore, is not subjected toany substantial quantity of sulphur and for this reason an improved procluct can be obtained.
As a specific example of the proportions which I have successfully used in carrying out my process I find that with a coal containing from 1 to 1.5 percent sulphur remainin therein, that suflicient limestone should e added to the oil to represent from 1 to 3 percent of calcium in the final coke. Generally one ton of the fuel oil is used with approximately four tons of coal. Before this oil is added to the coal, pulverized limestone of an impal able fineness, pref erably equal to the neness of the coal, which may be from 100 to 200 meshes per 'inch, is added to the oil, and if the coal is not exceedingly high in sulphur, this quantity of limestone would be sufiicient to perform the reaction herein described. As previously stated, however, the relative quantities may vary, depending upon the amount of sulphur'the coal contains, and also on the t pe of coal used, but with the usual-rune coking bituminous coals, the examples cessful.
The rocess may be applied to oils that are big in sulphur. for'the purpose of desulphurizing the oil'by first making the oil lime coal mixture then distilling out the oil as gases and condensible vapors.
Having thus described my invention what I claim is:
1. The herein described process, which given above have proven succonsists in mixing pulverized coal with 1 water, in adding pulverized lime to a liquid the pulverized coal to form an amalgamated mass.
2. The herein described process, which consists in introducing to hydrocarbon oils a quantity of finely pulverized limestone, and in intimately mixing said limestone with finely reduced coal to form an amalgamated mass of a plastic consistency.
'3. The herein described process, which consists in mixing a substance possessing the properties of lime with hydrocarbon oil, and in then agitating such materials with finely reduced coal to form a" plastic mass. Y Y
4. A process of the character described, consisting in comm-ingling hydrocarbon oil with finely pulverized coal having a sulphur content to form a substantially plastic mass, and in incorporating with the hydrocarbon oil an agent adapted to be thoroughly distributed throughout the plastic mass of coal and oil to intimately contact with the sulphur content of the coal and possessing the properties of forming with said sulphiu' when the mass is heated calcium sulphide.
- 5. A purifying proces, consisting in intimately mixing finely pulverized'coal containing a sulphur content and a hydrocarform with said sulphur when the mass is subjected to a coking. temperature calcium sulphide.
7. A purifying process, which consists in mixing comminuted coal,' hydrocarbon oil and reagent to form a homogeneous mass and to bring said reagent into intimate contact with the sulphur contained in the coal to remove said sulphur when the mass is subjected to acoking temperature.
8. A purifying process, which consists in mixing comminuted; coal, hydrocarbon oil and reagent to form a homogeneous mass and to bring said agent into intimate contact with the sulphur contained in the coal to remove said sulphur when the ma& is subjected to a coking temperature as calcium and sulphide compounds.
9. The herein described process consistaceous material. and oxides of the calcium group to form a homogeneous substantially plastic mass.
10..The herein described process which consists in mixing comminuted coal, a mineraloil, and oxides of the calcium group to form a homogeneous mass with said materials distributed throughout the same.
11. The herein described process consisting in thoroughly mixing a mineral oil with a' wet finely reduced comminuted' mineral carbonaceous material and pulverized oxides of the calcium group.
In testimony whereof I affix my signa- WALTER EDWIN TRENT.
US667046A 1923-10-06 1923-10-06 Process of producing coke Expired - Lifetime US1545620A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US667046A US1545620A (en) 1923-10-06 1923-10-06 Process of producing coke
FR586490D FR586490A (en) 1923-10-06 1924-09-24 Process for the production of coke

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US667046A US1545620A (en) 1923-10-06 1923-10-06 Process of producing coke

Publications (1)

Publication Number Publication Date
US1545620A true US1545620A (en) 1925-07-14

Family

ID=24676585

Family Applications (1)

Application Number Title Priority Date Filing Date
US667046A Expired - Lifetime US1545620A (en) 1923-10-06 1923-10-06 Process of producing coke

Country Status (2)

Country Link
US (1) US1545620A (en)
FR (1) FR586490A (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3661719A (en) * 1970-10-28 1972-05-09 John J Kelmar Non-polluting by-product coal carbonization plant
US4232615A (en) * 1979-06-11 1980-11-11 Aluminum Company Of America Coal burning method to reduce particulate and sulfur emissions
EP0030831A2 (en) * 1979-12-07 1981-06-24 Exxon Research And Engineering Company Coal combustion process
US4308808A (en) * 1979-06-11 1982-01-05 Aluminum Company Of America Coal burning method to reduce particulate and sulfur emissions
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
US4661240A (en) * 1979-06-08 1987-04-28 Alberta Research Council Low sulfur coke using dispersed calcium
US4940010A (en) * 1988-07-22 1990-07-10 Ogden-Martin Systems, Inc. Acid gas control process and apparatus for waste fired incinerators
US5092254A (en) * 1988-07-22 1992-03-03 Ogden-Martin Systems, Inc. Acid gas control process and apparatus for waste fired incinerators
US20060034743A1 (en) * 2004-08-16 2006-02-16 Premier Chemicals, Llc Reduction of coal-fired combustion emissions
US7731821B1 (en) * 2007-02-08 2010-06-08 Sesa Goa Limited Reduction of sulfur-containing gases during conversion of coal into metallurgical coke
WO2015082051A1 (en) * 2013-12-06 2015-06-11 Thyssenkrupp Industrial Solutions Ag Method and coke extraction plant for treating sulfur-containing process residues from crude oil processing; petroleum coke formed from sulfur-containing process residues

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3661719A (en) * 1970-10-28 1972-05-09 John J Kelmar Non-polluting by-product coal carbonization plant
US4661240A (en) * 1979-06-08 1987-04-28 Alberta Research Council Low sulfur coke using dispersed calcium
US4232615A (en) * 1979-06-11 1980-11-11 Aluminum Company Of America Coal burning method to reduce particulate and sulfur emissions
US4308808A (en) * 1979-06-11 1982-01-05 Aluminum Company Of America Coal burning method to reduce particulate and sulfur emissions
EP0030831A2 (en) * 1979-12-07 1981-06-24 Exxon Research And Engineering Company Coal combustion process
EP0030831A3 (en) * 1979-12-07 1981-11-04 Exxon Research And Engineering Company Improved coal combustion process
EP0184847A3 (en) * 1984-12-13 1988-03-09 Aluminum Company Of America Fuel burning method to reduce sulfur emissions and form non-toxic sulfur compounds
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
EP0184847A2 (en) * 1984-12-13 1986-06-18 Aluminum Company Of America Fuel burning method to reduce sulfur emissions and form non-toxic sulfur compounds
EP0184846A2 (en) * 1984-12-14 1986-06-18 Aluminum Company Of America Three-stage process for burning fuel containing sulfur to reduce emission of particulates and sulfur-containing gases
EP0184846A3 (en) * 1984-12-14 1988-03-02 Aluminum Company Of America Three-stage process for burning fuel containing sulfur to reduce emission of particulates and sulfur-containing gases
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
US4940010A (en) * 1988-07-22 1990-07-10 Ogden-Martin Systems, Inc. Acid gas control process and apparatus for waste fired incinerators
US5092254A (en) * 1988-07-22 1992-03-03 Ogden-Martin Systems, Inc. Acid gas control process and apparatus for waste fired incinerators
US20060034743A1 (en) * 2004-08-16 2006-02-16 Premier Chemicals, Llc Reduction of coal-fired combustion emissions
US7276217B2 (en) 2004-08-16 2007-10-02 Premier Chemicals, Llc Reduction of coal-fired combustion emissions
US7731821B1 (en) * 2007-02-08 2010-06-08 Sesa Goa Limited Reduction of sulfur-containing gases during conversion of coal into metallurgical coke
WO2015082051A1 (en) * 2013-12-06 2015-06-11 Thyssenkrupp Industrial Solutions Ag Method and coke extraction plant for treating sulfur-containing process residues from crude oil processing; petroleum coke formed from sulfur-containing process residues
RU2668907C1 (en) * 2013-12-06 2018-10-04 Тиссенкрупп Индастриал Солюшнз Аг Method and plant for producing coke by treating sulphur-containing process residues from crude oil processing, petroleum coke formed from sulphur-containing process residues

Also Published As

Publication number Publication date
FR586490A (en) 1925-03-27

Similar Documents

Publication Publication Date Title
US1545620A (en) Process of producing coke
US4032352A (en) Binder composition
JPH02163308A (en) Method for desulfurization of molten
US1923803A (en) Briquette and method of producing same
US3307927A (en) Process for the treatment of pulverulent material
DE69104664T2 (en) Additive for desulphurizing iron and process for introducing it into pig iron.
US2808325A (en) Process of refining pulverized metallic ores involving the production and use of ore pellets
US2028105A (en) Method of producing sponge iron
US2863755A (en) Oil-treated calcium carbide for desulfurization of iron
GB1473340A (en) Process for producing self-sufficient hot-coke briquettes for use in a metallurgical process
US3873427A (en) Desulfurizing coke using a ferruginous material and a metal chloride
US486100A (en) Sylvania
US4323392A (en) Agent for desulfurizing crude iron and steel melts, and process for making it
US1158366A (en) Process of making cohering masses.
US1729496A (en) Process of making briquettes or nonmolded lumps of comminuted minerals for metallurgical purposes and the product of said process
US1879373A (en) Method of utilizing certain by-products of iron and steel plants
DE3544563C2 (en) Means for desulfurizing molten iron
US780308A (en) Composition fuel.
US2880083A (en) Method of producing sponge iron
US520377A (en) Ernest nienstaedt
US3431103A (en) Process for the manufacture of ferrosilicon
RU2151738C1 (en) Charge for production of silicon and method of preparing molding material for production of silicon
US1129645A (en) Preparing ore for blast-furnaces.
US1562876A (en) Treatment of finely-divided coal and the production of briquettes
US708331A (en) Process of treating fine iron ores for blast-furnaces.