US3725241A - Solids removal from hydrogenated coal liquids - Google Patents

Solids removal from hydrogenated coal liquids Download PDF

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US3725241A
US3725241A US00206439A US3725241DA US3725241A US 3725241 A US3725241 A US 3725241A US 00206439 A US00206439 A US 00206439A US 3725241D A US3725241D A US 3725241DA US 3725241 A US3725241 A US 3725241A
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solids
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ash
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M Chervenak
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HRI Inc
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/08Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts
    • C10G1/083Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts in the presence of a solvent
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/04Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
    • C10G1/045Separation of insoluble materials

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  • ABSTRACT OF THE DISCLOSURE Better than fifty percent of the ash and associated solids from a coal-derived oil, such as a hydrogenated coal product, are removed by magnetic separation.
  • the ash and associated solids have been rendered magnetically susceptible by prior hydrogenation treatment.
  • coal-derived oil from the hydrogenation of coal by the expanded (ebullated) bed reaction process hereinbefore discussed while containing solids including ash and unconverted coal, if treated by conventional magnetic means can be freed of such solids up to as much as 98 percent.
  • the magnetic field strength for this invention should be at least about 5,000 gauss, and preferably greater than about 10,000
  • the viscosity of the solids-' containing liquid as fed to the magnetic separator device should not exceed about 500 centipoise and preferably should not exceed about 50 centipoise.
  • This liquid viscosity may be adjusted by varying either the liquid composition of the liquid-solids stream, or by varying its temperature, or both.
  • Usual operating condi-' tions for the liquid-solids stream from which the solids are magnetically separated are 400600 F. temperature and having a liquid viscosity of 2-10 centipoise.
  • the particle size of the ash solids in this liquid-solids stream will usually be smaller than about 200 mesh U.S. Std. sieve series, or smaller than about microns.
  • a coal such as bituminous, semibituminous, subbituminous or lignite
  • entering the system at 10 is first passed through a preparation unit generally indicated at 12.
  • a preparation unit generally indicated at 12.
  • the coal has a particle size of about 50 mesh (U.S. Std. screen) and finer.
  • a carrying oil indicated at 18 which, as hereinafter pointed out, is conveniently made in the system.
  • the ground coal should be mixed with at least about an equal weight of carrying oil.
  • the coal-oil slurry is pressurized by pump 20 to superatmospheric pressure such as 500-5000 p.s.i. partial pressure of hydrogen, and is then passed through heater 22 to bring the slurry up to a temperature in the order of 750 F. to 950 F., and preferably 800 F. to 900 F. Such heated slurry then discharges into the reactor feed line 26 wherein it is supplied with make-up hydrogen from line 28 as well as recycle hydrogen from line 46.
  • superatmospheric pressure such as 500-5000 p.s.i. partial pressure of hydrogen
  • a hydrogenation catalyst may be added to reactor 30 at 31 in the ratio of about 0.1 to 2.0 pounds of catalyst per ton of coal.
  • a catalyst would be from the class of cobalt, molybdenum, nickel, tin, iron and the like deposited on a base of the class of alumina, magnesia, silica, and the like and of a size at least inch and more frequently as extrudates in the range of to A1. inch, i.e., between about 3 and 14 mesh screens of the U.S. Std. scale. It is noted that the catalyst need not be added continuously nor is it required that it be in fine admixture with the coal.
  • a vessel containing a mass of solid particles of a contact material which may be a specific catalyst as above indicated, and expanding the mass of solid particles at least 10 percent over the volume of the stationary mass
  • the solid particles are Placed in random motion within the vessel by the upfiowing streams.
  • a mass of solid particles in this state of random motion in a liquid medium may be described as ebullated.
  • the characteristics of the ebullated mass at a prescribed degree of volume expansion can be such that a finer, lighter particulate solid will pass upwardly through the catalyst mass, so that the particles constituting the ebullated mass are retained in the reactor and the finer, lighter material may pass from the reactor.
  • the catalyst bed upper level 32 above which few, if any, particles ascend is called the upper level of ebullation.
  • the gross density of the stationary mass of contact material will be between about 25 and 200 pounds per cubic foot
  • the flow rate of the liquid will be between about to 120 gallons per minute per square foot of horizontal cross section of the ebullated mass
  • the expanded volume of the ebullated mass usually will be not more than about double the volume of the settled mass and preferably greater by at least about 30 percent.
  • a recycle liquid stream 34 which may be internal or external of the reactor, may be removed above the upper level of ebullation 32, and recycled by pump 36 to the bottom of the reactor 30 to maintain the desired superficial liquid velocity in the reactor.
  • Spent catalyst may be removed from time to time by drawoff 37.
  • Preferred reactor operating conditions are in the order of 800 to 900 F. and about 1000 to 3000 p.s.i. partial pressure of hydrogen.
  • Coal throughput or space velocity is at the rate of 15 to 150 pounds coal per hour per cubic foot of reactor space, so that the yield of unreacted coal as char is between 5 and 15 percent of the quantity of moisture and ash free coal feed.
  • the relative size of the coal and catalyst particles and conditions of ebullation are such that the catalyst is retained in the reactor, while the ash and unreacted char is carried out with the reaction products and the slurry oil solid.
  • the reactor eflluent stream 38 passing to high pressure separator 40 includes some gaseous fractions and is virtually free of solid particles of contact material, although it may contain ash and char in the liquid.
  • a gas stream is removed at 42 and then passed to absorber 44.
  • a hydrogen recycle in line 46 removed from absorber 44 may be returned to the reactor 30 to supplement the hydrogen requirements.
  • a liquid stream from the absorber 44 will be removed at 48 and this is joined with the liquid stream 49 from the high pressure separator 40.
  • the combined liquid stream is then passed to a low pressure recovery system 50.
  • the low pressure separator 50 operates at 500 to 650 F. and permits removal of a high B.t.u. heating value gaseous product at 52 and a solids-free liquid at 54. A separate bottoms liquid stream containing ash and char is removed at 56. A portion of the liquid from line 54 may be used as stream 18 to prepare the initial coal-oil slurry.
  • the solids-oil mixture in line 56 which usually has an ash concentration in the range of 5 to 15%, temperature of 450 to 600 F. and viscosity of 2 to 10 centipoise, is passed to magnetic separator 60 having a field strength of at least about 5000 gauss. It conveniently and preferably may be a standard rotary or drum type unit having an appropriate magnetizable surface suitably controlled by circuits to energize portions thereof during rotation. By applying the desired magnetic force to liquid stream 56, the oil portion may be removed at 62 and the magnetic ash portion removed at 64. Suitable scraper blades as recognized in the industry may be used.
  • the oil stream 62 may be passed to a second magnetic separator (not shown) by which further magnetic particles are removed.
  • Example 1 was verified in an experiment performed using a sample of coal-derived separator bottoms liquid containing particulate ash and unconverted coal solids, and designed to be functonally equivalent to actual process conditions.
  • This liquid material was extracted with benzene to dissolve the oil, then the dried particulate material was dispersed in a 6% weight/volume solution of benzene in a glass test tube at room temperature, which was held vertically between the poles of a magnet having a field strength of about 10,000 gauss. After a short time, e.g., about three minutes, the bulk of the particulat solids had settled to the bottom, but some solids remained clinging to the sides of the test tube adjacent the magnet poles. This latter material was removed for chemical analysis, and the procedure repeated. Results using two coal samples are given in the table below:
  • coal hydrogenation solids dispersed in benzene at room temperature comprise a liquid-solids mixture that was chosen to have approximately the same viscosity and to respond to a strong magnetic field in a substantially equivalent manner as the ash and unconverted coal solids dispersed in the actual separator bottoms oil at process temperatures of 450 to 600 F.
  • liquid-containing solids In addition to passing the liquid-containing solids at a suitable temperature (about 500 F.) and a dilution to a viscosity less than about 500 centipoise through a rotary type magnetic separator, so that the accumulated solids can be removed by scraping or demagnetizing, it is alternatively possible to pass the liquid through a magnetic grid or screen for separation. The accumulated solids can be removed therefrom by washing and/or demagnetizing.
  • the improvement in removing ash and unconverted solids from the liquid-solids eflluent, which improvement consists in passing the liquid-solids efiluent through a magnetic field of at least about 5,000 gauss to attract the magnetically sus ceptible particles, and recovering a liquid which is substantially solids-free.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

BETTER THAN FIFTY PERCENT OF THE ASH AND ASSOCIATED SOLIDS FROM A COATED-DERIVED OIL, SUCH AS A HYDROGENATED COAL PRODUCT, ARE REMOVED BY MAGNETIC SEPARATION. THE ASH AND ASSOCIATED SOLIDS HAVE BEEN RENDERED MAGNETICALLY SUSCEPTIBLE BY PRIOR HYDROGENATION TREATMENT.

Description

A ril 3, 1973 c. CHERVENAK SOLIDS REMOVAL FROM HYDROGENATEI) COAL LIQUIDS Filed Dec. 9. 1971 Hydrogen Recycle m V 46 r LT -44 5 4o 1 Absorber COOI j High Pressure Separator EL PELQHQL 3| 38 Drying Grinding Q Screening i 5 52 I8 -|4 Oil l "y 32," LOW 54 7 Pressure 2 Recovery Reoctor Spent 22 26 3 Magnetic 2% V 4 P SeporotorGO :51 62 Heater 28 Make up Oil 20 Hydrogen Ash 54 United States Patent O U.S. Cl. 208 7 Claims ABSTRACT OF THE DISCLOSURE Better than fifty percent of the ash and associated solids from a coal-derived oil, such as a hydrogenated coal product, are removed by magnetic separation. The ash and associated solids have been rendered magnetically susceptible by prior hydrogenation treatment.
BACKGROUND OF THE INVENTION As described in the U.S. Pat. No. 3,519,555, the hydrogenation of coal to more valuable products (both liquid and gas) utilizing relatively low reactor pressures and achieving better than 80 percent conversion of the coal thereby producing in the order of four barrels of oil per ton of coal makes available for the first time a nearly inexhaustible fuel source for commercially competitive fuels.
It is recognized, however, that such liquid (coal-derived oil) contains the ash and unconverted solids which frequently amount to to percent of the coal. It is quite apparent that such solids material must be removed from the oil if it is to have commercial value, and often this removal carries with it some additional fraction of the liquid product.
The usefulness of removing metallic contaminants from coal and ores by magnetic means is, of course, well known and there are many processes available and substantial prior patent art. For example, it is well known in the water washing of coal to utilize magnetic separation for removing metal such as tramp iron. In the Leeman patent, U.S. 2,998,882, it is suggested for example that magnetic separations of both coarse and fine particles can be accomplished to remove magnetite. In the later patent to Ergun U.S. 3,463,310, it is suggested that electromagnetic heating of the iron particles in coal tends to convert them to a magnetic form. He proposes to use microwave energy to convert pyrites to pyrrhotite, magnetite, etc. before magnetic separation. As pointed out, this avoids the need of the high conversion temperatures of 360 600 C. formerly thought necessary, and which would tend to undesirably remove coal volatiles. Utilization of energy frequencies of the order of 10 Hz. or greater for the volumes of coal in commercial operations is considered uneconomical. However, the removal of known magnetic particles even in liquid-coal mixtures has given no suggestion of applicability to coal solids in coal-derived liquids generated by hydrogenation.
SUMMARY OF THE INVENTION I have now found, however, that coal-derived oil from the hydrogenation of coal by the expanded (ebullated) bed reaction process hereinbefore discussed, while containing solids including ash and unconverted coal, if treated by conventional magnetic means can be freed of such solids up to as much as 98 percent. This was completely unexpected as the initial ash is commonly found to be non-magnetic and the extent to which there is any iron present is so small as to render magnetic separation substantially useless. It appears that the prior hydrogenation process influences the ash particles and renders them susceptible to removal by magnetic means.
While I am not certain of the phenomenon, it appears 3,725,241 Patented Apr. 3, 1973 ICE that the iron in the ash, which is probably originally in the form of ferric sulfide, is converted during the hydro genation to a reduced form and, in the magnetic field, it serves as a nucleus to carry with it other non-magnetic portions of the ash. A highly beneficial substantially solids-free liquid product is thus obtained.
There is of course a general relationship which exists between the magnetic susceptibility of the coal-derived particulate solids, the temperature and viscosity of the separator bottoms liquid, and the magnetic field strength required for effective separation of the solids therefrom. For particles which are only slightly magnetic, relatively high magnetic field strengths are required to effect a useful separation, particularly if the liquid is moderately to highly viscous. Increased temperature of the liquid and/ or use of normally less viscous liquid will permit somewhat lower field strengths to be effectively utilized for particle separation. To achieve useful separations the magnetic field strength for this invention should be at least about 5,000 gauss, and preferably greater than about 10,000
gauss. Also for useful results, the viscosity of the solids-' containing liquid as fed to the magnetic separator device should not exceed about 500 centipoise and preferably should not exceed about 50 centipoise.
This liquid viscosity may be adjusted by varying either the liquid composition of the liquid-solids stream, or by varying its temperature, or both. Usual operating condi-' tions for the liquid-solids stream from which the solids are magnetically separated are 400600 F. temperature and having a liquid viscosity of 2-10 centipoise. The particle size of the ash solids in this liquid-solids stream will usually be smaller than about 200 mesh U.S. Std. sieve series, or smaller than about microns.
While this invention appears to be applicable to various types of hydroconversion processes, wherein at least 50 weight percent conversion is accomplished, I find that the results from ebullated bed continuous hydrogenation process are exceptional, wherein in excess of weight percent conversions are obtained.
DESCRIPTION OF THE DRAWING The drawing is a schematic view of the relevant apparatus for coal hydrogenation.
DESCRIPTION OF THE PREFERRED EMBODIMENT This invention will now be described as used with an ebullated bed type hydrogenation process. As shown, a coal such as bituminous, semibituminous, subbituminous or lignite, entering the system at 10 is first passed through a preparation unit generally indicated at 12. In such a unit it is desirable to dry the coal of substantially all surface moisture and to grind the coal to a desired mesh and then to screen it for uniformity. For our purposes, it is preferable that the coal has a particle size of about 50 mesh (U.S. Std. screen) and finer.
The coal fines discharge at 14- into the transfer line 16 where the coal is blended with a carrying oil indicated at 18 which, as hereinafter pointed out, is conveniently made in the system. To establish an effective transportable slurry, it is found that the ground coal should be mixed with at least about an equal weight of carrying oil.
The coal-oil slurry is pressurized by pump 20 to superatmospheric pressure such as 500-5000 p.s.i. partial pressure of hydrogen, and is then passed through heater 22 to bring the slurry up to a temperature in the order of 750 F. to 950 F., and preferably 800 F. to 900 F. Such heated slurry then discharges into the reactor feed line 26 wherein it is supplied with make-up hydrogen from line 28 as well as recycle hydrogen from line 46.
The entire mixture of hydrogen and coal-oil slurry then enters one or more reactors 30, passing upwardly from the bottom at a rate and under pressure and at a temperature to accomplish the desired hydrogenation. In addition, a hydrogenation catalyst may be added to reactor 30 at 31 in the ratio of about 0.1 to 2.0 pounds of catalyst per ton of coal. Such a catalyst would be from the class of cobalt, molybdenum, nickel, tin, iron and the like deposited on a base of the class of alumina, magnesia, silica, and the like and of a size at least inch and more frequently as extrudates in the range of to A1. inch, i.e., between about 3 and 14 mesh screens of the U.S. Std. scale. It is noted that the catalyst need not be added continuously nor is it required that it be in fine admixture with the coal.
By concurrently flowing streams of liquid and gasiform materials upwardly through a vessel containing a mass of solid particles of a contact material, which may be a specific catalyst as above indicated, and expanding the mass of solid particles at least 10 percent over the volume of the stationary mass, the solid particles are Placed in random motion within the vessel by the upfiowing streams. A mass of solid particles in this state of random motion in a liquid medium may be described as ebullated. The characteristics of the ebullated mass at a prescribed degree of volume expansion can be such that a finer, lighter particulate solid will pass upwardly through the catalyst mass, so that the particles constituting the ebullated mass are retained in the reactor and the finer, lighter material may pass from the reactor. The catalyst bed upper level 32 above which few, if any, particles ascend is called the upper level of ebullation. v
In general, the gross density of the stationary mass of contact material will be between about 25 and 200 pounds per cubic foot, the flow rate of the liquid will be between about to 120 gallons per minute per square foot of horizontal cross section of the ebullated mass, and the expanded volume of the ebullated mass usually will be not more than about double the volume of the settled mass and preferably greater by at least about 30 percent. A recycle liquid stream 34, which may be internal or external of the reactor, may be removed above the upper level of ebullation 32, and recycled by pump 36 to the bottom of the reactor 30 to maintain the desired superficial liquid velocity in the reactor. Spent catalyst may be removed from time to time by drawoff 37.
Preferred reactor operating conditions are in the order of 800 to 900 F. and about 1000 to 3000 p.s.i. partial pressure of hydrogen. Coal throughput or space velocity is at the rate of 15 to 150 pounds coal per hour per cubic foot of reactor space, so that the yield of unreacted coal as char is between 5 and 15 percent of the quantity of moisture and ash free coal feed. The relative size of the coal and catalyst particles and conditions of ebullation are such that the catalyst is retained in the reactor, while the ash and unreacted char is carried out with the reaction products and the slurry oil solid.
The reactor eflluent stream 38 passing to high pressure separator 40 includes some gaseous fractions and is virtually free of solid particles of contact material, although it may contain ash and char in the liquid. From the separator 40, a gas stream is removed at 42 and then passed to absorber 44. A hydrogen recycle in line 46 removed from absorber 44 may be returned to the reactor 30 to supplement the hydrogen requirements. A liquid stream from the absorber 44 will be removed at 48 and this is joined with the liquid stream 49 from the high pressure separator 40. The combined liquid stream is then passed to a low pressure recovery system 50.
The low pressure separator 50 operates at 500 to 650 F. and permits removal of a high B.t.u. heating value gaseous product at 52 and a solids-free liquid at 54. A separate bottoms liquid stream containing ash and char is removed at 56. A portion of the liquid from line 54 may be used as stream 18 to prepare the initial coal-oil slurry.
The solids-oil mixture in line 56, which usually has an ash concentration in the range of 5 to 15%, temperature of 450 to 600 F. and viscosity of 2 to 10 centipoise, is passed to magnetic separator 60 having a field strength of at least about 5000 gauss. It conveniently and preferably may be a standard rotary or drum type unit having an appropriate magnetizable surface suitably controlled by circuits to energize portions thereof during rotation. By applying the desired magnetic force to liquid stream 56, the oil portion may be removed at 62 and the magnetic ash portion removed at 64. Suitable scraper blades as recognized in the industry may be used.
If a very high degree of ash separation is required, the oil stream 62 may be passed to a second magnetic separator (not shown) by which further magnetic particles are removed.
Example This invention was verified in an experiment performed using a sample of coal-derived separator bottoms liquid containing particulate ash and unconverted coal solids, and designed to be functonally equivalent to actual process conditions. This liquid material was extracted with benzene to dissolve the oil, then the dried particulate material was dispersed in a 6% weight/volume solution of benzene in a glass test tube at room temperature, which was held vertically between the poles of a magnet having a field strength of about 10,000 gauss. After a short time, e.g., about three minutes, the bulk of the particulat solids had settled to the bottom, but some solids remained clinging to the sides of the test tube adjacent the magnet poles. This latter material was removed for chemical analysis, and the procedure repeated. Results using two coal samples are given in the table below:
These coal hydrogenation solids dispersed in benzene at room temperature comprise a liquid-solids mixture that was chosen to have approximately the same viscosity and to respond to a strong magnetic field in a substantially equivalent manner as the ash and unconverted coal solids dispersed in the actual separator bottoms oil at process temperatures of 450 to 600 F.
Using a new sample of separator bottoms liquid-solids material, a new sample was prepared and several successive magnetic fractions were removed from the benzene dispersion using the above procedure. It was estimated that up to about 98% of the solids material could be removed from the liquid using this magnetic separation procedure.
Thus, these experiments demonstrated that an unexpected and useful separation of these fine ash solids from the separator bottoms oil stream resulting from coal hydrogenation can be made by magnetic means using field strength of at least 5,000 gauss.
On a sample of finely-ground feed coal sized to 200 mesh, it was found that about 98 percent was non-magnetic using the same equipment and technique.
In addition to passing the liquid-containing solids at a suitable temperature (about 500 F.) and a dilution to a viscosity less than about 500 centipoise through a rotary type magnetic separator, so that the accumulated solids can be removed by scraping or demagnetizing, it is alternatively possible to pass the liquid through a magnetic grid or screen for separation. The accumulated solids can be removed therefrom by washing and/or demagnetizing.
Prior experimentation which yielded the results indicated above on a hydrogenated coalderived oil resulting from the ebullated bed process leads me to believe that other hydrogenated coal-derived oils are substantially as susceptible to magnetic separation of ash. In such cases, the resulting ash would similarly be of about the same composition and thus susceptible to separation by magnetic means.
What I claim is:
1. In the hydrogenation of coal under liquid phase conditions in a reaction zone at a temperature in the range of 750 to 950 F. and superatmospheric pressure for a time sufficient to convert at least 50 weight percent of the coal to liquid and gaseous products, the improvement in removing ash and unconverted solids from the liquid-solids eflluent, which improvement consists in passing the liquid-solids efiluent through a magnetic field of at least about 5,000 gauss to attract the magnetically sus ceptible particles, and recovering a liquid which is substantially solids-free.
2. The process of claim 1 wherein the viscosity of said liquid-solids effluent stream does not exceed about 500 centipoise.
3. The process of claim 2, wherein the magnetic field strength is greater than about 10,000 gauss.
4. The process of claim 3 wherein the ash particles removed are smaller than 200 mesh U.S. Std. screen size.
5. The process of claim 1 wherein the hydrogenation is accomplished in the presence of a particulate hydrogenation catalyst and in which the coal in the presence of a liquid recovered from the process is passed upwardly through the reaction zone under ebullated bed conditions, and the ash concentration is in the range of 5 to 15 weight percent of the coal feed.
6. The process of claim 1 wherein the magnetic field is provided by a drum type magnetic separator.
7. The process of claim 1 wherein the magnetic field is provided by a grid type magnetic separator.
References Cited UNITED STATES PATENTS 1,512,870 10/1924 Ullrich et a1 209-214 2,998,882 9/1961 Leeman 209172.5 3,481,471 12/1969 Spodig 210222 DELBERT E. GANTZ, Primary Examiner S. BERGER, Assistant Examiner US. Cl. X.R. 208--8
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3976557A (en) * 1974-11-29 1976-08-24 Hydrocarbon Research, Inc. Pretreatment of coal-derived liquid to improve magnetic separation of solids
US3999958A (en) * 1974-03-05 1976-12-28 Joseph Iannicelli Coal beneficiation
US4052170A (en) * 1976-07-09 1977-10-04 Mobil Oil Corporation Magnetic desulfurization of airborne pulverized coal
US4342640A (en) * 1980-11-24 1982-08-03 Chevron Research Company Magnetic separation of mineral particles from shale oil
US4388179A (en) * 1980-11-24 1983-06-14 Chevron Research Company Magnetic separation of mineral particles from shale oil
US4406773A (en) * 1981-05-13 1983-09-27 Ashland Oil, Inc. Magnetic separation of high activity catalyst from low activity catalyst
US4495055A (en) * 1982-04-05 1985-01-22 Hri, Inc. Coal catalytic hydrogenation process using direct coal slurry feed to reactor with controlled mixing conditions
US5171424A (en) * 1990-10-22 1992-12-15 Ashland Oil, Inc. Magnetic separation of old from new cracking catalyst by means of heavy rare earth "magnetic hooks"
US5190635A (en) * 1989-04-03 1993-03-02 Ashland Oil, Inc. Superparamagnetic formation of FCC catalyst provides means of separation of old equilibrium fluid cracking catalyst
US5538624A (en) * 1994-10-21 1996-07-23 Ashland Inc. Process, apparatus and compositions for recycle of cracking catalyst additives

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3999958A (en) * 1974-03-05 1976-12-28 Joseph Iannicelli Coal beneficiation
US3976557A (en) * 1974-11-29 1976-08-24 Hydrocarbon Research, Inc. Pretreatment of coal-derived liquid to improve magnetic separation of solids
US4052170A (en) * 1976-07-09 1977-10-04 Mobil Oil Corporation Magnetic desulfurization of airborne pulverized coal
US4342640A (en) * 1980-11-24 1982-08-03 Chevron Research Company Magnetic separation of mineral particles from shale oil
US4388179A (en) * 1980-11-24 1983-06-14 Chevron Research Company Magnetic separation of mineral particles from shale oil
US4406773A (en) * 1981-05-13 1983-09-27 Ashland Oil, Inc. Magnetic separation of high activity catalyst from low activity catalyst
US4495055A (en) * 1982-04-05 1985-01-22 Hri, Inc. Coal catalytic hydrogenation process using direct coal slurry feed to reactor with controlled mixing conditions
US5190635A (en) * 1989-04-03 1993-03-02 Ashland Oil, Inc. Superparamagnetic formation of FCC catalyst provides means of separation of old equilibrium fluid cracking catalyst
US5171424A (en) * 1990-10-22 1992-12-15 Ashland Oil, Inc. Magnetic separation of old from new cracking catalyst by means of heavy rare earth "magnetic hooks"
US5538624A (en) * 1994-10-21 1996-07-23 Ashland Inc. Process, apparatus and compositions for recycle of cracking catalyst additives

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