AU2014297503B2 - Production method for reformed coal - Google Patents

Production method for reformed coal Download PDF

Info

Publication number
AU2014297503B2
AU2014297503B2 AU2014297503A AU2014297503A AU2014297503B2 AU 2014297503 B2 AU2014297503 B2 AU 2014297503B2 AU 2014297503 A AU2014297503 A AU 2014297503A AU 2014297503 A AU2014297503 A AU 2014297503A AU 2014297503 B2 AU2014297503 B2 AU 2014297503B2
Authority
AU
Australia
Prior art keywords
coal
deashed
dried
dry
production method
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.)
Ceased
Application number
AU2014297503A
Other versions
AU2014297503A1 (en
Inventor
Kenji Atarashiya
Tsutomu Hamada
Masakazu Sakaguchi
Fumiaki Sato
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries Ltd
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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Publication of AU2014297503A1 publication Critical patent/AU2014297503A1/en
Application granted granted Critical
Publication of AU2014297503B2 publication Critical patent/AU2014297503B2/en
Ceased legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • C10L9/08Treating solid fuels to improve their combustion by heat treatments, e.g. calcining
    • 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
    • C10B57/10Drying
    • 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
    • C10L5/04Raw material of mineral origin to be used; Pretreatment 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
    • C10L9/00Treating solid fuels to improve their combustion
    • 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
    • C10L2250/00Structural features of fuel components or fuel compositions, either in solid, liquid or gaseous state
    • C10L2250/06Particle, bubble or droplet size
    • 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
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/02Combustion or pyrolysis
    • 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
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/06Heat exchange, direct or indirect
    • 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
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/08Drying or removing water
    • 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
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/24Mixing, stirring of fuel components
    • 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
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/28Cutting, disintegrating, shredding or grinding
    • 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
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/40Applying a magnetic field or inclusion of magnets in the apparatus
    • 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
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/54Specific separation steps for separating fractions, components or impurities during preparation or upgrading of a fuel

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Geology (AREA)
  • Geochemistry & Mineralogy (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Materials Engineering (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Coke Industry (AREA)

Abstract

The purpose of the present invention is to increase the calorific value, and to obtain coal having further reduced mercury content. The method involves carrying out a drying step (S1) in which coal (1) of low grade is dried to obtain dry coal (2); a dry deashing step (S2) in which the ash component (6) is eliminated from the dry coal (2) obtained in the drying step (S1), by a dry deashing means to obtain deashed dry coal (3); and a carbonization step (S3) in which the deashed dry coal (3) obtained in the dry deashing step (S2) is carbonized to obtain deashed carbonized coal (4).

Description

PRODUCTION METHOD OF REFORMED COAL
[0001]
The present invention relates to a production method of reformed coal.
[0002]
Low-grade coal (low-rank coal) with high moisture content, such as lignite and sub-bituminous coal, has a low calorific value per unit of weight; thus, such coal is heated so as to be dried and pyrolyzed and is also modified in a low-oxygen atmosphere so as to reduce surface activity. As a result, the coal is converted to reformed coal having a high calorific value per unit of weight while preventing spontaneous combustion (see, for example, Patent Document 1).
[0003]
It is also known that mercury can be removed in coal reformation processes involving such pyrolysis described above through heating operation during pyrolysis (see. for example. Patent Document 2). ]0004]
Patent Document 1: Japanese Unexamined Patent Application Publication No. 2011-37937A Patent Document 2: US Patent No. 5403365B Patent Document 3: US Patent No. 8394240B Patent Document 4: US Patent No. 7540384B
[0005]
Non Patent Document 1: R. Weinstein and R. Snoby, "Advances in dry jigging improves coal quality", p.29 to p.34, Mining Engineering. January 2007 Non Patent Document 2: William H. Pollock et al., "Lowering Costs with Dry Coal Cleaning Technology to Meet New Environmental Requirements", p.l to p,13, presented at the 10th Anniversary CoalGen Conference, Pittsburgh. PA. August 10, 2010 [0006]
However, although the coal reformation process described above is capable of obtaining reformed coal by removing mercury from the raw coal through pyrolysis, there is a demand for coal having a lower mercury content.
[0007]
Embodiments of the present invention have been conceived in order to solve the problem described above, and provide a production method of reformed coal in which coal having a higher calorific value and lower mercury content can be obtained.
[0008]
The invention provides a production method of reformed coal, the method comprising a drying step of drying coal to obtain dried coal, a drying deashing step of removing ash from the dried coal obtained in the drying step to obtain deashed dried coal and a pyrolyzing step of pyrolyzing the deashed dried coal obtained in the dry deashing step to obtain deashed pyrolized coal.
[0009]
Embodiments of the invention include a dividing step of dividing out a portion of the deashed dried coal obtained in the dry deashing step; and a mixing step of mixing the deashed dried coal divided out in the dividing step with the deashed pyrolyzed coal obtained in the pyrolyzing step to obtain mixed coal.
[0010]
Preferably the dry deashing step is performed using a pulverizer that pulverizes the dried coal and a magnetic separation apparatus that magnetically separates and removes the ash from the dried coal pulverized by the pulverizer.
[0011]
Preferably, the dry deashing step is performed using an air stream separation apparatus that, with an air stream, separates and removes the ash from the dried coal.
[0012]
In certain embodiments of the invention, the coal is low-grade coal.
[0013]
In accordance with the production method of reformed coal according to embodiments of the present invention, it is possible to increase a calorific value of coal by drying and dry deashing the coal, before pyrolyzing the coal. In addition, removing ash from the dried coal through dry deashing before pyrolyzing the dried coal allows for the removal of both the ash and mercury contained within the dried coal, resulting in deashed pyrolyzed coal having a mercury content lower than that of pyrolyzed coal obtained by pyrolyzing dried coal. As a result, coal having a higher calorific value and a lower mercury content can be obtained.
[0013A]
The present invention will now be described, by way ot non-limiting example only, with reference to the accompanying drawings as briefly described below.
[0014] FIG. 1 is a process flow chart of a first embodiment of a production method of reformed coal according to embodiments of the present invention. FIG. 2 is a process flow chart of a second embodiment of the production method of reformed coal according to embodiments of the present invention.
[0015]
Embodiments of a production method of reformed coal according to the present invention will now be described with reference to the drawings. However, the present invention is not limited to the embodiments described hereafter witii reference to the drawings.
[0016] [First Embodiment] A first embodiment of the production method of reformed coal according to the present invention will now be described with reference to FIG. 1.
[0017]
The production method of reformed coal according to the present embodiment includes, as illustrated in FIG. 1, a drying step SI of drying low-grade coal (low-rank coal) 1 to obtain dried coal 2, a dry deashing step S2 of dry-deashing the dried coal 2 obtained in the drying step SI using a dry deashing apparatus to obtain deashed dried coal 3, and a pyrolyzing step S3 of pyrolyzing the deashed dried coal 3 obtained in the dry deashing step S2 to obtain deashed pyrolyzed coal 4.
[0018]
The low-rank coal 1 is coal having a high (60 to 70%) moisture content, such as lignite or sub-bituminous coal, which, although vast deposits thereof exist, the coal has a low calorific value per unit of weight and is inefficient to transport.
[0019]
The drying step SI is a step of removing water 5 from the low-rank coal 1. In the drying step SI, for example, feeding the low-rank coal 1 to a hot-air dryer of belt conveyor type or the like and drying the low-rank coal 1 with hot air (100 to 280°C, preferably 150 to 200°C) produces dried coal 2 having a moisture content of substantially 0%.
[0020]
The dry deashing step S2 is a step of separating and removing, from the dried coal 2, ash 6 contained in the dried coal 2. In the dry deashing step S2, for example, feeding the dried coal 2 to a dry deashing apparatus provided with a pulverizer that pulverizes the dried coal 2 and a magnetic separation apparatus that magnetically separates and removes the ash 6 from the dried coal 2 pulverized by the pulverizer, and pulverizing the dried coal 2 to, for example, a particle diameter of 200 mesh or less and magnetically separating and removing the ash 6 (especially pyrite and the like having a high mercury content) produces deashed dried coal 3 having, for example, an ash content of about 35% or less. Alternatively, in the dry deashing step S2, for example, feeding the dried coal 2 to the dry deashing apparatus, such as an air stream separation apparatus, allowing the dried coal 2 to flow on a fluidized bed and supplying air thereto to separate and remove the ash 6 (especially substances including high-mercury-content pyrite, which are heavier than the coal) produces the deashed dried coal 3 having an ash content of, for example, about 35% or less. In other words, the dry deashing step S2 produces deashed dried coal 3 obtained by removing, from the dried coal 2, ash 6 along with the better part of the mercury in the dried coal 2.
[0021]
The apparatus disclosed, for example, in Non Patent Document 1 can be used as the dry deashing apparatus provided with the pulverizer and the magnetic separation apparatus. The apparatus disclosed, for example, in Patent Document 4 or Non Patent Document 2 can be used as the dry deashing apparatus such as the air stream separation apparatus.
[0022]
The pyrolyzing step S3 is a step of removing volatile components 7 such as tar from the deashed dried coal 3. In the pyrolyzing step S3, for example, feeding the deashed dried coal 3 to a continuous pyrolyzer and pyrolyzing the deashed dried coal 3 at an elevated temperature (300 to 500°C, preferably 400 to 450°C) to separate and collect mercury contained in the deashed dried coal 3 along with the volatile components 7 such as tar produces deashed pyrolyzed coal 4.
[0023]
Thus, in accordance with the production method of reformed coal according to the present embodiment, it is possible to dry, dry deash, and pyrolyze the low-rank coal 1 to obtain deashed pyrolyzed coal 4, thereby allowing for a higher calorific value than that of the low-rank coal 1. In addition, mercury in the low-rank coal 1 can be removed in both the dry deashing step S2 and the pyrolyzing step S3, with the mercury being physically removed along with the ash 6 in the dry deashing step S2 before being removed along with the volatile components 7, thereby allowing the deashed pyrolyzed coal 4 to have a lower mercury content than that of pyrolyzed coal obtained by drying and pyrolyzing the low-rank coal 1. As a result, deashed pyrolyzed coal 4 having a higher calorific value and a lower mercury content can be obtained.
[0024] [Second Embodiment] A second embodiment of the production method of reformed coal according to the present invention will now be described with reference to FIG. 2.
The present embodiment is constituted by the steps of the production method of reformed coal illustrated in FIG. 1 to which a dividing step and a mixing step are added. The rest of the steps is substantially identical to that illustrated in FIG. 1 as described above, so the identical steps and substances will be given the same reference numerals and duplicated description thereof will be omitted as appropriate.
[0025]
The production method of reformed coal according to the present embodiment includes, as illustrated in FIG. 2, a drying step SI of drying low-grade coal (low-rank coal) 1 to obtain dried coal 2, a dry deashing step S2 of dry deashing the dried coal 2 obtained in the drying step SI using a dry deashing apparatus to obtain deashed dried coal 3, a dividing step Sll of dividing out a portion of the deashed dried coal 3 obtained in the dry deashing step S2, a pyrolyzing step S12 of pyrolyzing deashed dried coal 3a that has not been divided out in the dividing step Sll to obtain deashed pyrolyzed coal 11, and a mixing step S13 of mixing the deashed pyrolyzed coal 11 obtained in the pyrolyzing step S12 with deashed dried coal 3b that has been divided out in the dividing step Sll to obtain mixed coal 12.
[0026]
The dividing step Sll is a step of dividing out a portion of the deashed dried coal 3. In the dividing step Sll, for example, feeding the deashed dried coal 3 to a dividing apparatus such as a conveyer belt or a screw feeder divides the deashed dried coal 3 into the deashed dried coal 3a to be sent to the pyrolyzing step S12 and the deashed dried coal 3b to be sent to the mixing step SI 3. The proportion of how the deashed dried coal 3 is divided can be adjusted according to the target oxygen content or mercury content of the mixed coal 12. This is because the oxygen content or mercury content of the deashed dried coal 3 and the deashed pyrolyzed coal 11 can be adjusted in accordance with respective processing conditions, and can also be determined through analysis.
[0027]
The pyrolyzing step S12 is a step, identical to the pyrolyzing step S3 described above, of removing volatile components 13 such as tar from the deashed dried coal 3a. In the pyrolyzing step S12, for example, feeding the deashed dry coal 3a to a continuous pyrolyzer, pyrolyzing the deashed dry coal 3a at an elevated temperature (300 to 500°C, preferably 400 to 45G°C), and separating and collecting mercury contained in the deashed dried coal 3a along with the volatile components 13 such as tar, produces deashed pyrolyzed coal 11.
[0028]
The mixing step SI 3 is a step of mixing the deashed pyrolyzed coal 11 obtained in the pyrolyzing step S12 with the deashed dried coal 3b divided out in the dividing step Sll. In the mixing step SI3, feeding the deashed dried coal 7 3b divided out in the dividing step S 11 into a mixer along with the deashed pyrolyzed coal 11 and stirring until the two are uniformly mixed produces mixed coal 12.
[0029]
The mixing ratio of the deashed pyrolyzed coal 1 1 to the deashed dried coal 3b in the mixture are adjusted, as appropriate, according to the respective oxygen content of the deashed pyrolyzed coal 1! and the deashed dried coal 3b, the respective mercury contents ofthe deashed pyrolyzed coal II and the deashed dried coal 3b, and the like. This is because the oxygen content and mercury content of the deashed dried coal 3 can be obtained through the processing condition of the dry deashing step S2 or analysis, and the oxygen content and mercury content of the deashed pyrolyzed coal 11 can be obtained through the processing condition of the pyrolyzing step S12 or analysis.
[0030]
Thus, in accordance with the production method of reformed coal according to the present embodiment, it is possible to mix the deashed pyrolyzed coal 11 obtained by drying, dry deashing, and pyrolyzing the lowrank coal 1 with divided out deashed dried coal 3b to obtain the mixed coal 12, thereby allowing for a higher calorific value than that of the low-rank coal 1. In addition, because the mixed coal 12 is a mixture ofthe deashed pyrolyzed coal 11 obtained by removing mercury from the low-rank coal 1 through dry deashing and pyrolysis and the deashed dried coal 3b obtained by removing mercury from the low-grade coal 1 through dry deashing, with the dry deashing physically removing mercury and the pyrolysis uniformly chemically removing mercury from the entirety ofthe coal, the mercury content of the deashed pyrolyzed coal 11 can be reduced to less than that of pyrolyzed coal obtained by drying and pyrolyzing the low-rank coal 1. As a result, the deashed pyrolyzed coal 11 having a higher calorific value and a Sower mercury content can be obtained. In addition, because the volume of the deashed dried coal 3b to be mixed can be increased according to the respective oxygen content and mercury content of the deashed pyrolyzed coal 1 1 and the deashed dry coal 3b and the target oxygen content and mercury content of the mixed coal 12, the yield can be increased over the production method of reformed coal according to the first embodiment, which does not include the dividing step S 11 and the mixing step S13, resulting in higher productivity ofthe mixed coal 12.
[0031]
Examples performed in order to confirm the effects of the production method of reformed coal according to embodiments of the present invention will now be described; however, the present invention is not limited to the examples described below with reference to various data. 8 [0032]
In the present embodiment, low-rank coal having a mercury content of 69 ppm is used. The low-rank coal is dried with hot air at a temperature of, for example, 100 to 280°C in the drying step to remove water from the low-rank coal and obtain dried coal. As only the water has been removed from the low-rank coal, the mercury content of the dried coal is 69 ppm, which is the same as the low-rank coal.
[0033]
Next, in the dry deashing step, the dried coal is pulverized to 200 mesh or less and the ash is magnetically removed therefrom, for example, by a dry deashing apparatus provided with a pulverizer and a magnetic separation apparatus, and deashed dried coal is obtained. As a result, the ash constituting a portion of the dried coal is removed. The ash is a substance such as pyrite having magnetic properties, which contains more mercury than the other substances in the coal. The mercury content of the deashed dried coal 3 is 24.2 ppm. The size of the finely powdered ash-containing dried coal was set so as to allow 98% of the calorific value of the coal to be retained while reducing mercury content by 65%. In other words, the dry deashing step physically removes the mercury contained in the dried coal.
[0034]
Next, in the dividing step, a portion of the deashed dried coal is divided out. The remainder of the deashed dried coal is pyrolyzed in the pyrolyzing step at an elevated temperature (300 to 500°C, preferably 400 to 450°C) to obtain deashed pyrolyzed coal. As a result, the mercury contained in the deashed dried coal is volatilized along with the volatile components, and removed by 80%. The mercury content of the deashed pyrolyzed coal is 4.83 ppm. In other words, the pyrolyzing step chemically removes the mercury contained in the deashed dried coal.
[0035]
Next, the deashed dried coal divided out in the dividing step and the deashed pyrolyzed coal obtained in the pyrolyzing step are mixed to obtain mixed coal. The divided out deashed dried coal and the deashed pyrolyzed coal obtained in the pyrolyzing step are mixed at the ratio of, for example. 54% by weight to 46% by weight to obtain the mixed coal. The mercury content of the obtained mixed coal is 13.8 ppm.
[0036]
Thus, it was apparent that oxygen content and mercury content can be adjusted by adjusting the particle size of the dried coal and the amount of ash to be removed in the dry deashing step and the mixing ratio of deashed pyrolyzed coal and deashed dried coal in the mixing step, thereby obtaining mixed coal having a higher calorific value and a lower mercury content.
[0037] [Other Embodiments]
In the first embodiment, the production method of reformed coal in which the low-rank coal 1 is dried, dry deashed, and pyrolyzed to obtain the deashed pyrolyzed coal 4 has been described, but a production method of reformed coal in which coal is obtained from the deashed pyrolyzed coal 4 having its surface deactivated through a deactivating process in which the deashed pyrolyzed coal 4 is brought into contact with a specific treatment gas (oxygen-containing gas) is also possible. In addition, a production method of reformed coal is also possible in which, after the coal obtained by the deashed pyrolyzed coal 4 having its surface deactivated through the deactivation process in which the deashed pyrolyzed coal 4 is brought into contact with a specific treatment gas (oxygen-containing gas), the coal is mixed with a binder such as corn starch or asphalt and compressed (at a pressure of 1,200 kg/cm2 and a temperature of 300 to 450°C, preferably 350 to 450°C) into a solid briquette such as a cylinder or a charcoal briquette to produce formed coal.
[0038]
In the second embodiment described above, the production method of reformed coal has been described in which the deashed dried coal 3a obtained by drying and dry deashing the low-rank coal 1 is pyrolyzed to obtain the deashed pyrolyzed coal 11, a portion of the deashed dried coal 3 is divided out, and the deashed pyrolyzed coal 11 and the divided out deashed dried coal 3b are mixed to obtain the mixed coal 12, but a production method of reformed coal in which coal is obtained by the mixed coal 12 having its surface deactivated through a deactivation process in which the mixed coal 12 is brought into contact with a specific treatment gas (oxygen-containing gas) is also possible. In addition, a production method of reformed coal is also possible in which, after the coal is obtained by the mixed coal 12 having its surface deactivated through the deactivation process in which the mixed coal 12 is brought into contact with a specific treatment gas (oxygen-containing gas), the coal is mixed with a binder such as corn starch or asphalt and compressed (at a pressure of 1,200 kg/cm2 and a temperature of 300 to 450°C, preferably 350 to450°C) into a solid briquette such as a cylinder or a charcoal briquette to produce formed coal.
[0039]
The production method of reformed coal according to embodiments of the present invention can obtain coal having a high calorific value and a lower mercury content, and thus can be used to great advantage in industrial applications.
Reference Signs List [0040] 1 Low-grade coal (low-rank coal) 2 Dried coal 3 Deashed dried coal 3a, 3b Deashed dried coal 4 Deashed pyrolyzed coal 5 Water 6 Ash 7 Volatile component 11 Deashed pyrolyzed coal 12 Mixed coal 13 Vo lati le component 51 Drying step 52 Dry deash ing step 53 Pyrolyzing step 511 Dividing step 512 Pyrolyzing step 513 Mixing step [0041]
While various embodiments of the present invention have been described above, it should be understood that they have been presented by way of example only, and not by way of limitation. It will be apparent to a person skilled in the relevant art that various changes in form and detail can be made therein without departing from the spirit and scope of the invention. Thus, the present invention should not be limited by any of the above described exemplary embodiments.
[0042]
Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
[0043]
The reference in this specification to any prior publication (or information derived from it). 01 to any matter which is known, is not, and should not be taken as an acknowledgment or admission 01 any form of suggestion that that prior publication (or information derived from it) or known mallei forms part of the common general knowledge in the field of endeavour to which this specificatior relates.

Claims (5)

  1. CLAIMS [Claim 1] A production method of reformed coal, the method comprising: a drying step of drying coal to obtain dried coal; a dry deashing step of removing ash from the dried coal obtained in the drying step to obtain deashed dried coal; and a pyrolyzing step of pyrolyzing the deashed dried coal obtained in the dry deashing step to obtain deashed pyrolyzed coal. [Claim
  2. 2] The production method of reformed coal according to claim 1, further comprising: a dividing step of dividing out a portion of the deashed dried coal obtained in the dry deashing step; and a mixing step of mixing the deashed dried coal divided out in the dividing step with the deashed pyrolyzed coal obtained in the pyrolyzing step to obtain mixed coal. [Claim
  3. 3] The production method of reformed coal according to claim 1 or 2, wherein the dry deashing step is performed using a pulverizer that pulverizes the dried coal and a magnetic separation apparatus that magnetically separates and removes the ash from the dried coal pulverized by the pulverizer. [Claim
  4. 4] The production method of reformed coal according to claim 1 or 2, wherein the dry deashing step is performed using an air stream separation apparatus that, with an air stream, separates and removes the ash from the dried coal. [Claim
  5. 5] The production method of reformed coal according to any one of claims 1 to 4, wherein the coal is low-grade coal.
AU2014297503A 2013-07-31 2014-07-16 Production method for reformed coal Ceased AU2014297503B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2013-158714 2013-07-31
JP2013158714A JP2015030737A (en) 2013-07-31 2013-07-31 Method for manufacturing modified coal
PCT/JP2014/068852 WO2015016062A1 (en) 2013-07-31 2014-07-16 Production method for reformed coal

Publications (2)

Publication Number Publication Date
AU2014297503A1 AU2014297503A1 (en) 2016-02-11
AU2014297503B2 true AU2014297503B2 (en) 2016-08-25

Family

ID=52431602

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2014297503A Ceased AU2014297503B2 (en) 2013-07-31 2014-07-16 Production method for reformed coal

Country Status (6)

Country Link
US (1) US20160160141A1 (en)
JP (1) JP2015030737A (en)
CN (1) CN105408459A (en)
AU (1) AU2014297503B2 (en)
DE (1) DE112014003532T5 (en)
WO (1) WO2015016062A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9777235B2 (en) 2016-04-04 2017-10-03 Allard Services Limited Fuel oil compositions and processes
AU2017246680B2 (en) 2016-04-04 2021-02-04 Arq Ip Limited Solid-liquid crude oil compositions and fractionation processes thereof
WO2019236871A1 (en) * 2018-06-07 2019-12-12 The Tru Shrimp Company Raceways and systems thereof
GB201815791D0 (en) * 2018-09-27 2018-11-14 Arq Ip Ltd Processes for utilisation of purified coal compositions as a chemical and thermal feedstock and cleaner burning fuel
CN110423628A (en) * 2019-09-09 2019-11-08 重庆润科新材料技术有限公司 A kind of low order dry distillation of coal process units and method

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0940980A (en) * 1995-07-25 1997-02-10 Toshihiko Maruyama Method for dry coal preparation and apparatus therefor
JP2011037937A (en) * 2009-08-07 2011-02-24 Mitsubishi Heavy Ind Ltd Method for producing modified coal

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4242102A (en) * 1978-12-15 1980-12-30 The Lummus Company Production of gasified products from ash containing bitumen produced in coal liquefaction
JPS5896695A (en) * 1981-12-02 1983-06-08 Mitsubishi Heavy Ind Ltd Process for dry deashing of coal
JPH09151386A (en) * 1995-11-29 1997-06-10 Mitsubishi Heavy Ind Ltd Magnetic separation of powdered coal
CN101155642A (en) * 2005-04-11 2008-04-02 脉动波有限公司 Methods for reduction pollutants from carbonaceous materials prior to combustion
CN102159324A (en) * 2007-07-19 2011-08-17 微煤公司 Method and system for separation of contaminants from coal
CN102492518A (en) * 2011-11-30 2012-06-13 中国五环工程有限公司 Quality-improving process and apparatus for high-ash low rank coal

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0940980A (en) * 1995-07-25 1997-02-10 Toshihiko Maruyama Method for dry coal preparation and apparatus therefor
JP2011037937A (en) * 2009-08-07 2011-02-24 Mitsubishi Heavy Ind Ltd Method for producing modified coal

Also Published As

Publication number Publication date
CN105408459A (en) 2016-03-16
US20160160141A1 (en) 2016-06-09
DE112014003532T5 (en) 2016-04-14
JP2015030737A (en) 2015-02-16
AU2014297503A1 (en) 2016-02-11
WO2015016062A1 (en) 2015-02-05

Similar Documents

Publication Publication Date Title
AU2014297503B2 (en) Production method for reformed coal
US8070839B2 (en) Briquetting process
US3619376A (en) Method of making metallurgical coke briquettes from coal, raw petroleum coke, inert material and a binder
GB2103653A (en) Method of producing coke briquettes
EP0020057A1 (en) Method and apparatus for producing char and gases from coal
JP2010222475A (en) Method for utilizing biomass
US2677650A (en) Carbonization of agglomerative coals
JP2015030738A (en) Method for manufacturing modified coal
CN102822317B (en) Process for production of solid fuel for use in sintering, solid fuel for use in sintering, and process for manufacturing sintered ore using same
JP2015030736A (en) Method for manufacturing modified coal
CN101781594A (en) Method and device for converting solid waste into fuel or energy
RU2651827C1 (en) Method of dry beneficiation of high-ash coal
EA201700186A1 (en) METHOD OF OBTAINING COKE
JP2011032370A (en) Iron ore-containing coke and method for producing the iron ore-containing coke
CN205709943U (en) Pyrolysis waste water is utilized to process the system of coal
RU2653509C9 (en) Coke fuel briquette
GB253878A (en) Improvements in carbonising coal
RU2381287C2 (en) Restorative for thermal-electric metallurgical processes
CN110305679A (en) A kind of coking process for the dry/wet coal mixing that can stablize moisture-free coal treating capacity
USRE24574E (en) welinsky
RU2087527C1 (en) Method of manufacturing coal briquets
WO2023129090A3 (en) Method for using biomass in coking coal blend
JP5761314B2 (en) How to use biomass
CN103725301A (en) New combined technique for simultaneously preparing tar, phenol and water gas
PL442937A1 (en) Sachet ethylene absorber with biomass torrefied bed and application of the sachet ethylene absorber

Legal Events

Date Code Title Description
FGA Letters patent sealed or granted (standard patent)
MK14 Patent ceased section 143(a) (annual fees not paid) or expired