US2869992A - Preliminary heating of fluid coke briquettes - Google Patents

Preliminary heating of fluid coke briquettes Download PDF

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US2869992A
US2869992A US632207A US63220757A US2869992A US 2869992 A US2869992 A US 2869992A US 632207 A US632207 A US 632207A US 63220757 A US63220757 A US 63220757A US 2869992 A US2869992 A US 2869992A
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briquettes
range
coke
oxygen
temperature
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US632207A
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James W Brown
Edward A Destremps
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering 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
    • C10L5/00Solid fuels
    • C10L5/02Solid fuels such as briquettes consisting mainly of carbonaceous materials of mineral or non-mineral origin
    • C10L5/26After-treatment of the shaped fuels, e.g. briquettes
    • C10L5/28Heating the shaped fuels, e.g. briquettes; Coking the binders

Description

Jan. 20, 1959 J. w. BROWN ET AL PRELIMINARY HEATING OF FLUID COKE BRIQUETTES v Filed Jan. 2, 1957 m Q s T w 55 E 52m m VJWLLL m m5 #5. 96 Em; F m m $26 5.
s r O t n e V .m p w n w me BD A Sm ea w ME By '2'. MM Attorney imately 15 to 30 Wt.
aired PRELMINARY HEATING F FLUID COKE BRHQUETTES James W. Brown, Mountainside, and Edward A. Bee tramps, Cranford, N. 3., assignors to Essa Research and Engineering Company, a corporation of Delaware Application January 2, 1957, Serial No. 632,207 4 Claims; (Cl. 44- -10) quettes are heat, hardened in a two-stage process while closely controlling the oxygen content of the treating gases.
There has recently been developed an improved process .known as the fluid coking process for the production of fluid coke and the thermal conversion of heavy hydrocarbon oils to lighter fractions, e. g., see U. S. Patents 2,725,349 and 2,721,169. For completeness the process is described in further detail below although it should be understood that the fluid coking process itself is no part of this invention.
The fluid coking unit consists basically of a reaction vessel or coker and a heater or burner vessel. In a typical operation the heavy oil to be processed is injected into the reaction vessel containing a dense, turbulent, fluidized bed of hot inert solid particles, preferably coke particles. A transfer line or staged reactors can be employed. Uniform temperature exists in the coking bed. Uniform mixing in the bed results in virtually isothermal conditions and effects instantaneous distribution ofthe feed stock. In the reaction zone the feed stock is partially vaporized and partially cracked. Effiuent vapors are removed from the coking vessel and sent to a fractionator for the recovery of gas and light distillates therefrom. Any heavy bottoms is usually returned to the coking vessel. The coke produced in the process re mains in the bed coated on the solid particles. Stripping steam is injected into the stripper to remove oil from the coke particles prior to the passage of the coke to the burner.
The heat for carrying out the endothermic coking reaction is generated in the burner vessel, usually but not necessarily separate. A stream of coke is thus transferred from the reactor to the burner vessel, such as a transfer. line or fluid bed' burner, employing a standpipe and riser'system'; air being supplied to the-riser for-conveyin'g the solids to the burner. Suificient coke or'addecl carbonaceous matter is burned in the 'burningyessel to bring the solids therein up to a temperaturesufiicient to maintain the system in heat balance. The burner solids are maintained at a higher temperaturethan the solids in the reactor. About 5% of coke, based on the feed, is burned for this purpose.- This may amount to approxercent of-thecoke made in the process. The net colte'production, which represents the coke made less the coke burned, is Withdrawn.
Heavy hydrocarbcnoilfeeds suitable for the coking process include heavy 'crudes, atmospheric and crude vacuum bottoms, pitch, asphalt, other heavy hydrocarbon petroleum residue or mixtures thereof. Typically such feeds can have an initial boiling point of about 700 F. or higher, an A. P. Lgravity ofabout'O" to120, and
a Conradson'carbon residue content of about 5 to 40 Estates Patent 1 each other.
- 2 wt. percent. (As to Couradson carbon residue see A. S. T.-M. test D-189-41.) Y
A problem in the marketing of the fluid coke product is the small size of the particles, predominantly, i. e., about 90 wt. percent, in the range of 20 to mesh. The production of substantially larger particles is inconsistent "ith satisfactory operation of the fluid bed. On the other hand industrial requirements for coke often necessitate particles having a diameter of about at least /8 inch to 1 inch.
,These fluid coke particles have accordinglybeen compacted into briquettes using various carbonaceous binder substances. The agglutinating carbonaceous binder-substances that can be utilized include suitable hydrocarbon binders, such as asphalt and other heavy pertoleum res idues, aromatic tars, e. g. vacuum reduced thermal tars,
heavy ends of coal tar, such as'coal tar pitches having about 5 to 25 wt. percentbased on the coke charge and preferably 5 to 15 wt. percent. The binder can also be admixed with steam in an amount of 1 to 10 wt. percent to produce a finely atomized spray which makes for better mixing with the coke particles. The binder can also be air blown to raise its melting point. The Hawkins :coker bottoms, for example, has a softening point of around F. which can be too low. About 3.0 ft,
of 425 F. air per pound of binder is required.
The fluid coke can be used as is to make briquettes, butthe behavior of briquettes during heating and the strength of the final products are improved by grinding part or all of the coke to produce finer particles. The
,optirnumtemperaturefor binder mixing with the coke is .one at which the-binder had a viscosity in the range of l000to 5000 centipoises, for example 2500 centipoises. Thebriquetting should be done at a temperature slightly above the softening point ofthe binder or binders utilized, i. e. conveniently at a temperature in the range of to 200 F, for example-l75 F. The mixture is then briquetted by molding in a press at a pressure of about 2100 to 20,000p. s. i. Rollpresses such as those commonly :employed to make briquettes from coaland other materials can be used. Such machines are described in the article Agglomeration, Chemical Engineering, October 1951, pages 161-165. The mixtures pass directly to the pressing rolls.
These briquettes require heat hardening at a temperature of above 700 F. to decompose the binder to a'car- --bonaceous residue and to produce adequate strength and cohesion. Treating atthese temperatures, however, because of the melting of the binder material results in the .,.deformation of the compactions and also adherence to In addition elevated temperatures tend to oxidize the compactions undersirably to form H 0 and these ditficulties. Some of them deal with particular ways coke which overcomes these difficulties.
Several methods have been proposed to overcome of conducting a preliminary heat hardeningstepso as to avoid subsequent deformation in the higher tempera- "than satisfactory quality.
This invention provides an improved method of thermally and chemically hardening compactions of fluid comprises subjecting; the fluid ,coke briquettes to twostages' of heat treatment. In thefirst, preliminary or ouring stage. they aretreated withan oxygen-containing:gas
The method zone at a lower portion thereof.
containing 2 to volume percent of oxygen at a temperature in the range of 400 to 1100 F. while in the form of a fixed bed of controlled depth. The rate of flow of the oxygen-containing gas as well as the time are carefully controlled. After this treatment the briquettes are allowed to cool and stand so as to relieve internal stresses. They are then heated while in the form of a downward, moving bed to a temperature in the range of 1400 to 2000 F. by countercurrent contact with hot inert gases. The control features are elaborated upon below, and all of them are necessary in combination in order to achieve the improved results of this invention.
In the first or preliminary stage of heating the briquettes are contacted with gas at a temperature in the range of 400 to 1100 F. while the briquettes are in the form of a fixed bed. The term fixed bed connotes a body of the briquettes supported by direct contact with each other and the retaining walls. Thus the coke particles can be and preferably are treated in the form of a fixed bed while on a moving grate. The bed depth is carefully controlled in order to avoid burning and therefore a depth of about 6 inches to 1 foot are utilized.
The oxygen content of the treating gas is quite important and is kept at 2 to 10 volume percent, preferably 5 volume percent, with the rest inerts such as N CO CO, etc. This operation has been found to be very critical with excessive temperatures or oxygen concentration causing combustion of briquettes and binder while less oxidizing conditions cause the briquettes to melt before sufficient oxidation has occurred to harden the binder by dehydrogenation. The amount of oxygen containing gas utilized is 5 to 5000 s. c. f./ cu. ft. of briquettes, preferably 1000. This is the minimum necessary for heat transfer rate and uniformity of treatment. The preliminary heating is conducted for a time interval of 10 to 60 minutes, preferably minutes. The flow of the oxygencontaining gas is frequently reversed, e. g., upflow for one half the indicated time and downflow for the remainder. This is obtained by the use of baflles to reverse the flow of gas through the moving grate.
The thus treated briquettes are then allowed to cool to a temperature in the range of 400 to 700 F. for about 5 to 20 minutes to relieve internal stresses. Experiments showed that briquettes were otherwise too brittle to handle on a conveyor.
The briquettes are then fed to a vertical elongated heat treatment zone conveniently a shaft furnace. They are there heated while in the form of a downward, moving bed to a temperature in the range of 1400 to 2000 F. for a heating time interval of about /2 hour to 5 hours. The requisite temperature is provided by countercurrent This invention will be better understood by reference to the following example and flow diagram shown in the drawing.
Referring now to the flow diagram, coke briquettes prepared as previously explained are sent through hopper 1 and conduit 2 on the moving grate 3 which is conveniently feet long and 4 feet wide. The grate passes through curing oven 4. The briquettes are treated on the grate by hot gas at 900 F. which contains 5 volume percent oxygen. The gas is passed upward through the first half of the grate and downward through the second half. Baliles located above and below the moving grate cause flow reversal as in the shell side of a heat exchanger. This oxygen-containing gas is prepared by controlled combustion of fuel gas such as, e. g. methane, through line 5 in burner a. Air or other oxygen-containing gas is supplied for the combustion through lines 7 and 8 with inert gas entering the burner through line 9 to dilute the oxygen concentration to 5 volume percent. The treating gas is vented through line 10. The curing gas rate is 1000 s. c. f.-/cu. ft. of briquettes. The bed depth of the coke briquettes which can be considered a fixed bed as previously described on a moving grate is about 1 foot. The velocity of the grate is maintained such that the preliminary heating is conducted for 30 minutes.
The thus treated briquettes are then discharged into bucket elevator 11. During this transportation they are allowed to stand and cool for 10 minutes to a temperature of 500 F. so as to relieve internal stresses. They are then fed through lines 12 and 13 into a vertical elongated second stage heating zone 14 conveniently a shaft furnace. Hot upwardly flowing flue gas from burner 15 countercurrently contacts the descending cured briquettes which are in the form of a falling, moving bed. The gases are at a superficial velocity of 5 ft./sec. Heating is at the rate of 9 F. per minuteso that the briquettes are heated to 1740 F. in 2.3 hours. The .tail gas is removed through line 16 and the hot briquettes are withdrawn through line 17.
Scrubbed tail gas can be recycled to the bottom of heating zone 14 to cool the briquettes, pick up heat and improve heat economy.
The advantages of this invention are shown in' the following example.
EXAMPLE ,1
A number of preliminary heat treating tests were made in which fixed shallow beds of briquettes made with coker bottoms were contacted with oxygen-containing gas at temperatures of 425 F. and 900 F. Minimum strength during heat treatment was measured.
contact with hot inert gases, which enter the heat treating The hot inert gases include materials like CO CO, N etc. Preferably the inert gases are flue gases from combustion systems. Combustible material can be fluid coke itself or an extraneous fuel such as fuel oid or natural gas. The combustion is supported by an oxygen containing gas such as air but preferably no oxygen contacts the briquettes. The superficial velocity of the inert gases is in the range of 3 to 15 ft/sec. so that the birquettes flow downwardlyin the form of a moving bed countercurrently thereto.
These data show that a relatively high temperature, around 900 F., is required to obtain hardening in a short time and to maintain sufficient minimum strength so that a fixed bed of briquettes can be supported.
At 900 F. it is necessary to limit the oxygen concentration to about 5 to 10% so as to avoid combustion.
EXAMPLE 2 The conditions for minimum curing gas consumption at 900 F. with5% oxygen were next determined in a. large heat treating furnace and are shown in Table II.
5 Table 11 GAS RATES REQUIRED TO HARDEN FIXED BED OF BRIQUETTES AT 900 F. T 20 LB. MINIMUM STRENGTH was found possible to achieve minimum gas consumption at 33 s. c. f. m. per cu. ft. of briquettes and 11" bed depth. Lower gas rates and higher bed depth were unsatisfactory because of non-uniform heat hardenmg.
These examples show that specific conditions can be selected with the specified ranges to minimize treating time and combustion of the briquettes. The briquettes then have sufficient strength to undergo the subsequent heat treating step.
The conditions usually encountered in a fluid coker for fuels are also listed below so as to further illustrate how the fluid coke was prepared.
CONDITIONS IN FLUID COKER REACTOR Broad Preferred Range Range Temperature, F 850-1, 200 9001. 000 Pressure, Atmospheres 110 1. 2 Superficial Velocity of Fluldizing Gas, it./sec.. 0. 2-10 0. 5-4 Coke Circulation (Solids/O11 Ratio) 2-30 7-15 The advantages of this invention will be apparent to the skilled in the art. Very strong briquettes are prepared in an economical manner with a minimum of deformation, loss of product or combustion.
It is to be understood that this invention is not limited to the specific examples which have been ofiered merely as illustrations and that modifications may be made without departing from the spirit of the invention.
What is claimed is:
1. A process for heat hardening briquettes of fluid coke with an agglutinating carbonaceous binder substance at temperatures at which the briquettes normally tend to deform and oxidize which comprises the steps of heating the briquettes while in the form of a fixed bed having a depth in the range of about 6 inches to 1 foot for a time interval in the range of 10 to minutes with an oxygen-containing gas at a temperature of 400 to 1100 F. and having an oxygen content in the range of about 2 to 10 volume percent. the amount of oxygen-containing gas utilized being in the range of about 5 to 5000 s. c. f./cu. ft. briquettes; cooling the thus treated briquettes to a temperature in the range of about 400 to 700 F. for a time interval of 5 to 20 minutes whereby internal stresses are removed and heating the briquettes while in p References Cited in the file of this patent UNITED STATES PATENTS Maurel July 4, 1939 Findlay Nov. 9, 1954

Claims (1)

1. A PROCESS FOR HEAT HARDENING BRIQUETTES OF FLUID COKE WITH AN AGGLUTINATING CARBONACEOUS HARDER SUBSTANCE AT TEMPERATURES AT WHICH THE BRIQUETTES NORMALLY TEND TO DEFORM AND OXIDIZE WHICH COMPRISES THE STEPS OF HEATING THE BRIQUETTES WHILE IN THE FORM OF A FIXED BED HAVING A DEPTH IN THE RANGE OF ABOUT 6 INCHES TO 1 FOOT FOR A TIME INTERVAL IN THE RANGE OF 10 TO 60 MINUTES WITH AN OXYGEN-CONTAINING GAS AT A TEMPERATURE OF 400* TO 1100* F. AND HAVING AN OXYGEN CONTENT IN THE RANGE OF ABOUT 2 TO 10 VOLUME PERCENT, THE AMOUNT OF OXYGEN-CONTAINING GAS UTILIZED BEING IN THE RANGE OF ABOUT 5 TO 5000 S.C.F./CU.FT. BRIQUETTES; COOLING THE THUS TREATED BRIQUETTES TO A TEMPERATURE IN THE RANGE OF ABOUT 400* TO 700* F. FOR A TIME INTERVAL OF 5 TO 20 MINUTES WHEREBY INTERNAL STRESSES ARE REMOVED AND HEATING THE BRIQUETTES WHILE IN THE FORM OF A DOWNWARD, MOVING BED TO A TEMPERATURE IN THE RANGE OF 1400* TO 2000* F. BY COUNTERCURRENT CONTACT WITH HOT INERT GASES.
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3140242A (en) * 1960-08-03 1964-07-07 Fmc Corp Processes for producing carbonaceous materials from high oxygen coals
US3140241A (en) * 1959-06-18 1964-07-07 Fmc Corp Processes for producing carbonaceous materials
US3172823A (en) * 1965-03-09 Process for hardening carbonaceous briquettes
US3184293A (en) * 1960-05-24 1965-05-18 Fmc Corp Carbonaceous shapes
DE1234188B (en) * 1959-09-26 1967-02-16 Metallgesellschaft Ag Process for oxidative hardening and degassing of briquettes
DE1262219B (en) * 1959-09-10 1968-03-07 Houilleres Bassin Du Nord Tunnel furnace for the three-stage heat treatment of briquettes made of coal and tar
US9278314B2 (en) 2012-04-11 2016-03-08 ADA-ES, Inc. Method and system to reclaim functional sites on a sorbent contaminated by heat stable salts
US9352270B2 (en) 2011-04-11 2016-05-31 ADA-ES, Inc. Fluidized bed and method and system for gas component capture

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2164933A (en) * 1934-11-07 1939-07-04 Maurel Invest Corp Process of baking fuel briquettes
US2694038A (en) * 1950-07-10 1954-11-09 Phillips Petroleum Co Method for manufacturing coke

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2164933A (en) * 1934-11-07 1939-07-04 Maurel Invest Corp Process of baking fuel briquettes
US2694038A (en) * 1950-07-10 1954-11-09 Phillips Petroleum Co Method for manufacturing coke

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3172823A (en) * 1965-03-09 Process for hardening carbonaceous briquettes
US3140241A (en) * 1959-06-18 1964-07-07 Fmc Corp Processes for producing carbonaceous materials
DE1421258B1 (en) * 1959-06-18 1972-09-21 Fmc Corp Process for the production of shaped coke from coals of any kind
DE1262219B (en) * 1959-09-10 1968-03-07 Houilleres Bassin Du Nord Tunnel furnace for the three-stage heat treatment of briquettes made of coal and tar
DE1234188B (en) * 1959-09-26 1967-02-16 Metallgesellschaft Ag Process for oxidative hardening and degassing of briquettes
US3184293A (en) * 1960-05-24 1965-05-18 Fmc Corp Carbonaceous shapes
US3140242A (en) * 1960-08-03 1964-07-07 Fmc Corp Processes for producing carbonaceous materials from high oxygen coals
US9352270B2 (en) 2011-04-11 2016-05-31 ADA-ES, Inc. Fluidized bed and method and system for gas component capture
US9278314B2 (en) 2012-04-11 2016-03-08 ADA-ES, Inc. Method and system to reclaim functional sites on a sorbent contaminated by heat stable salts

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