WO2018186003A1 - Procédé de production de particules de carbone poreux et particules de carbone poreux - Google Patents

Procédé de production de particules de carbone poreux et particules de carbone poreux Download PDF

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WO2018186003A1
WO2018186003A1 PCT/JP2018/002240 JP2018002240W WO2018186003A1 WO 2018186003 A1 WO2018186003 A1 WO 2018186003A1 JP 2018002240 W JP2018002240 W JP 2018002240W WO 2018186003 A1 WO2018186003 A1 WO 2018186003A1
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solvent
porous carbon
coal
carbon particles
polymer compound
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PCT/JP2018/002240
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English (en)
Japanese (ja)
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濱口　眞基
祥平 和田
聡則 井上
豊田　昌宏
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株式会社神戸製鋼所
国立大学法人大分大学
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2/00—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic
    • B01J2/02—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by dividing the liquid material into drops, e.g. by spraying, and solidifying the drops
    • B01J2/04—Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic by dividing the liquid material into drops, e.g. by spraying, and solidifying the drops in a gaseous medium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/20—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising free carbon; comprising carbon obtained by carbonising processes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/30—Processes for preparing, regenerating, or reactivating
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00—Carbon; Compounds thereof
    • C01B32/05—Preparation or purification of carbon not covered by groups C01B32/15, C01B32/20, C01B32/25, C01B32/30
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00—Processes of treating or compounding macromolecular substances
    • C08J3/12—Powdering or granulating

Definitions

  • the present invention relates to a method for producing porous carbon particles and porous carbon particles.
  • porous carbon particles having pores with a diameter of micron or nanometer order on the surface and a high specific surface area are useful as adsorbents.
  • a carbon raw material is activated with water vapor or an alkaline substance to increase the specific surface area
  • an organic resin is an oxide such as magnesium oxide (template)
  • a method of removing the oxide after mixing with carbon and carbonizing the particles (Japanese Patent Laid-Open No. 2016-41656).
  • the conventional method for producing porous carbon particles in addition to the step of carbonizing the raw material, a step of performing an activation treatment with an alkaline substance and a removal treatment of the template particles is necessary, which increases the production cost and the production efficiency. Decreases. Further, the pores formed by these treatments tend to have larger diameters as they are closer to the surface of the porous carbon particles. For this reason, the conventional porous carbon particles have relatively small pores (mesopores) having a diameter of 2 nm or more and less than 50 nm or pores (macropores) having a diameter of 50 nm or more than pores (micropores) having a diameter of less than 2 nm. It has many, and its specific surface area is low with respect to denseness. Therefore, in the conventional method for producing porous carbon particles, there is room for improvement in production cost, production efficiency, and specific surface area.
  • the present invention has been made based on the circumstances as described above, and aims to provide a method for producing porous carbon particles having relatively high production efficiency and production cost and a large specific surface area, and porous carbon particles. To do.
  • porous carbon particles As a result of intensive studies on a method for producing porous carbon particles, the present inventors spray-dried a solution in which ashless coal and a polymer compound are dissolved in a solvent, so that the porous carbon particles have micropores and It has been found that it has a relatively large number of mesopores and can increase its specific surface area. Moreover, the present inventors have learned that porous carbon particles can be produced by this production method by spray drying without performing activation treatment or treatment with template particles, and have completed the present invention.
  • the invention made to solve the above problems includes a step of spray-drying a solution in which ashless coal and a polymer compound are dissolved in a solvent, and a step of heat-treating the solid content obtained in the spray-drying step.
  • the solvent contains oxygen atoms or nitrogen atoms, and has a boiling point at atmospheric pressure of 50 ° C. or higher and lower than 250 ° C., and a method for producing porous carbon particles mainly comprising an organic compound.
  • the method for producing the porous carbon particles uses ashless coal as a carbon material. Since ashless coal has a higher carbonization yield than coal and petroleum pitch, the production method of the porous carbon particles has high production efficiency of the porous carbon particles. In the method for producing porous carbon particles, in the spray drying process, the solvent is rapidly desorbed from the state in which ashless coal is dissolved, so that a large number of micropores are induced in the obtained solid content. Moreover, since the ratio of heteroelements, such as oxygen, is high in the ashless coal used as the main component of the said solid compared with coal and petroleum pitch, it is hard to carry out crystal growth at the time of heat processing. For this reason, micropores are maintained in the heating process.
  • the mesopores in the solid content mainly increase due to decomposition and dissipation of the polymer compound during carbonization in the heating step.
  • a solvent containing an organic compound containing oxygen atoms or nitrogen atoms and having a boiling point at atmospheric pressure within the above range as a main component is used. Since the ashless coal and the polymer compound can be dissolved in such a solvent at a high concentration, the production efficiency can be increased. Therefore, by using the method for producing porous carbon particles, porous carbon particles having relatively high production efficiency and production cost and a large specific surface area can be produced.
  • the content of ashless coal in the above solution is preferably 5% by mass or more and 50% by mass or less.
  • a step of mixing coal and a solvent, a step of eluting components soluble in the solvent from the coal in the slurry obtained in the mixing step, and the slurry after elution in the elution step May be further provided with a step of separating the solvent into a liquid component containing a solvent-soluble component and a solvent-insoluble component, and a step of mixing a polymer compound with the liquid component.
  • Ashless coal can be eluted into the solvent by solvent extraction of coal in the elution step. Therefore, the production cost of the porous carbon particles can be further reduced by using a solution in which the polymer compound is mixed with the liquid component in which the ashless coal is dissolved in the solvent.
  • the spray pressure and the liquid feeding speed may be adjusted so that the average diameter of the solid content is 1 ⁇ m or more and 20 ⁇ m or less.
  • the specific surface area of the porous carbon particles can be further increased by adjusting the spray pressure and the liquid feeding speed so that the average diameter of the solid content is within the above range.
  • the content of the polymer compound relative to the total amount of the ashless coal and the polymer compound is preferably 1% by mass or more and 15% by mass or less.
  • Another invention made in order to solve the above-mentioned problems is provided with a carbon layer containing carbon as a main component and enclosing a hollow portion, the carbon layer having a plurality of pores, and a specific surface area of 200 cm 2 / g or more. It is the porous carbon particle which is.
  • the porous carbon particles have a carbon layer that encloses the hollow portion, the pores are more likely to penetrate the carbon layer than the solid porous carbon particles, and the diameter of each pore is the distance from the surface. It is easy to make it uniform regardless. For this reason, even if it is a micro hole, a hole is maintained to a comparatively deep position from an outer surface, without a diameter being crushed in the middle. Moreover, since the said specific surface area is more than the said minimum, the said porous carbon particle is excellent in porosity.
  • main component means a component having the largest content, for example, a component having a content of 50% by mass or more, and “average diameter of solid content” is the same volume as the solid content. It means the diameter of a true sphere.
  • porous carbon particles having a large specific surface area can be produced with relatively good production efficiency and production cost.
  • the porous carbon particle of this invention has a large specific surface area, it can be used suitably as an adsorbent or an electronic component.
  • FIG. 1 is a schematic flow diagram showing a method for producing porous carbon particles according to an embodiment of the present invention. It is a schematic flowchart of the spray-drying process of FIG. It is a schematic flowchart which shows the manufacturing method of the porous carbon particle which concerns on embodiment different from FIG.
  • the method for producing porous carbon particles mainly includes a spray drying step S1 and a heating step S2, as shown in FIG.
  • the production method of the porous carbon particles mainly includes, for example, a coal supply unit, a solvent supply unit, a mixing unit, a temperature raising unit, an elution unit, a separation unit, a spraying unit, and a heating unit. It can be done by the device.
  • spray drying process S1 solid content is obtained by spray drying of the solution in which ashless coal and a high molecular compound are dissolved.
  • the spray drying step S1 includes a first mixing step S11, an elution step S12, a solid-liquid separation step S13, a second mixing step S14, and a solid content generating step S15.
  • This 1st mixing process S11 can be performed by a coal supply part, a solvent supply part, and a mixing part, for example.
  • the coal supply unit supplies coal to the mixing unit.
  • a coal supply part well-known coal hoppers, such as a normal pressure hopper used in a normal pressure state, a pressure hopper used in a normal pressure state and a pressurization state, can be used.
  • Coal supplied from the coal supply unit is coal that is a raw material for ashless coal.
  • various quality coals can be used.
  • bituminous coal with a high extraction rate of ashless coal or cheaper low-grade coal (subbituminous coal or lignite) is preferably used.
  • finely pulverized coal means coal having a mass ratio of coal having a particle size of less than 1 mm to 80% or more of the mass of the entire coal.
  • lump coal can also be used as coal supplied from a coal supply part.
  • particle size refers to a value measured in accordance with JIS-Z8815: 1994 general screening test rules. For sorting according to the particle size of coal, for example, a metal net sieve specified in JIS-Z8801-1: 2006 can be used.
  • the lower limit of the carbon content of the low-grade coal is preferably 70% by mass.
  • the upper limit of the carbon content of the low-grade coal is preferably 85% by mass, and more preferably 82% by mass.
  • coal supplied to a mixing part from a coal supply part you may use the coal which mixed a small amount of solvent and made it slurry.
  • the coal By supplying the slurried coal from the coal supply unit to the mixing unit, the coal is easily mixed with the solvent in the mixing unit, and the coal can be dissolved more quickly.
  • the amount of the solvent to be mixed at the time of forming the slurry is large, the amount of heat for raising the slurry to the elution temperature in the temperature raising portion described later becomes unnecessarily large, which may increase the manufacturing cost.
  • the solvent supply unit supplies the solvent to the mixing unit.
  • the said solvent supply part has a solvent tank which stores a solvent, and supplies a solvent from this solvent tank to a mixing part.
  • the solvent supplied from the solvent supply unit is mixed with coal supplied from the coal supply unit in the mixing unit.
  • the solvent supplied from the solvent supply unit is mainly composed of an organic compound containing an oxygen atom or a nitrogen atom.
  • an organic compound containing an oxygen atom or a nitrogen atom may be one kind, and two or more kinds of organic compounds may be mixed.
  • the lower limit of the boiling point of the solvent at atmospheric pressure is 50 ° C., more preferably 60 ° C., and still more preferably 65 ° C.
  • the boiling point of the solvent is less than 250 ° C, more preferably less than 210 ° C, and even more preferably less than 160 ° C. If the boiling point of the solvent is less than the lower limit, the ashless coal may not be sufficiently dissolved and the content of ashless coal may not be increased. Conversely, if the boiling point of the solvent is equal to or higher than the upper limit, the pressure associated with the desorption of the solvent is insufficient in the solid content generation step S15, so that the pores of the porous carbon particles may not be sufficiently formed.
  • the mixing unit mixes the coal supplied from the coal supply unit and the solvent supplied from the solvent supply unit.
  • a preparation tank can be used as the mixing unit.
  • the coal and solvent are supplied to the preparation tank through a supply pipe.
  • the preparation tank the supplied coal and solvent are mixed to prepare a slurry.
  • the said preparation tank has a stirrer, and maintains the mixing state of a slurry by hold
  • the lower limit of the coal concentration is preferably 5% by mass and more preferably 10% by mass.
  • the upper limit of the coal concentration is preferably 65% by mass, and more preferably 40% by mass. If the coal concentration is less than the lower limit, the elution amount of the solvent-soluble component eluted in the elution step S12 is less than the slurry processing amount, and therefore the content of ashless coal contained in the solution is insufficient. There is a risk. Conversely, if the coal concentration exceeds the upper limit, the solvent-soluble component is likely to be saturated in the solvent, and the elution rate of the solvent-soluble component may be reduced.
  • elution step S12 coal components soluble in the solvent are eluted from the coal in the slurry obtained in the first mixing step S11.
  • the elution step S12 can be performed by the temperature raising part and the elution part.
  • the temperature raising unit raises the temperature of the slurry obtained in the first mixing step S11.
  • the temperature raising part is not particularly limited as long as it can raise the temperature of the slurry passing through the inside, and examples thereof include a resistance heating heater and an induction heating coil. Further, the temperature raising unit may be configured to raise the temperature using a heat medium, for example, has a heating tube disposed around the flow path of the slurry passing through the inside, and the heating tube The slurry may be heated by supplying a heat medium such as steam or oil.
  • the temperature of the slurry after the temperature rise by the temperature raising unit is appropriately determined according to the solvent to be used. If the temperature of the slurry is less than the lower limit, the elution rate may decrease. On the other hand, if the temperature of the slurry exceeds the upper limit, the solvent is excessively vaporized, which may make it difficult to control the concentration of the slurry.
  • the pressure of the temperature raising portion is not particularly limited, but can be normal pressure (0.1 MPa).
  • An elution part elutes a coal component soluble in a solvent from coal in a slurry obtained by the above-mentioned mixing part and heated at the above-mentioned temperature raising part.
  • an extraction tank can be used, and the slurry after the above temperature rise is supplied to this extraction tank.
  • the coal components soluble in the solvent are eluted from the coal while maintaining the temperature and pressure of the slurry.
  • the extraction tank has a stirrer. The elution can be promoted by stirring the slurry with this stirrer.
  • the elution time at the elution part is not particularly limited, but is preferably 10 minutes or more and 70 minutes or less from the viewpoint of the extraction amount of the solvent-soluble component and the extraction efficiency.
  • Solid-liquid separation process In the solid-liquid separation step S13, the slurry that has been eluted in the elution step S12 is separated into a liquid component containing a solvent-soluble component and a solvent-insoluble component.
  • This solid-liquid separation step S13 can be performed by a separation unit.
  • the solvent-insoluble component refers to an extraction residue that mainly contains ash and insoluble coal insoluble in the extraction solvent, and further contains an extraction solvent in addition to these.
  • Separatation part As a method for separating the liquid component and the solvent-insoluble component in the separation unit, for example, a gravity sedimentation method, a filtration method, and a centrifugal separation method can be used, and a sedimentation tank, a filter, and a centrifugal separator are used, respectively.
  • the gravitational sedimentation method is a separation method in which a solvent-insoluble component is settled by using gravity in a sedimentation tank to separate it into solid and liquid.
  • the liquid component containing the solvent-soluble component is accumulated in the upper part of the sedimentation tank. This liquid content is filtered using a filter unit as necessary, and then discharged to a spraying section to be described later.
  • the solvent-insoluble component is discharged from the lower part of the separation part.
  • the liquid component including the solvent-soluble component and the solvent-insoluble component can be discharged from the sedimentation tank while continuously supplying the slurry into the separation unit. Thereby, continuous solid-liquid separation processing becomes possible.
  • the time for maintaining the slurry in the separation part is not particularly limited, but can be, for example, 30 minutes or more and 120 minutes or less, and sedimentation separation in the separation part is performed within this time.
  • the time which maintains a slurry in a separation part can be shortened.
  • the temperature and pressure in the separation unit can be the same as the temperature and pressure of the slurry after the temperature is raised by the temperature raising unit.
  • the main component of the solvent-soluble component contained in the liquid is ashless coal.
  • Ashless coal has an ash content of 5% by mass or less or 3% by mass or less, hardly contains ash, has no moisture, and exhibits a higher calorific value than, for example, raw coal.
  • by-product coal can be obtained by evaporating and separating the solvent from the solvent-insoluble component.
  • By-product charcoal does not show softening and melting properties, but the oxygen-containing functional groups are eliminated. Therefore, by-product coal does not inhibit the softening and melting properties of other coals contained in this blended coal when used as a blended coal. Therefore, this blended coal can be used, for example, as a part of the blended coal of the coke raw material. Further, by-product coal may be used as fuel in the same manner as general coal.
  • ⁇ Second mixing step> the polymer compound is mixed with the liquid component in which the ashless coal obtained in the solid-liquid separation step S13 is dissolved. By this dissolution, a solution in which the ashless coal and the polymer compound are dissolved is obtained.
  • the polymer compound is not particularly limited as long as a solvent that can be dissolved with ashless coal is present, but an organic polymer compound is preferable, and an organic polymer compound having a carbon yield lower than that of ashless coal is preferable. preferable. Since the carbon yield of ashless coal is usually 30% by mass or more and 70% by mass or less, the upper limit of the carbon yield of the polymer compound is preferably 25% by mass, more preferably 15% by mass, and more preferably 5% by mass. Is more preferable. By using a polymer compound having a low carbon yield in this way, the mesopore increasing effect in the heating step S2 described later can be easily promoted.
  • the lower limit of the carbon yield of the polymer compound is not particularly limited, and may be 0% by mass.
  • examples of such a polymer compound include polymethyl methacrylate (carbon yield 4% by mass), polyvinylpyrrolidone (carbon yield 0% by mass), polystyrene (carbon yield 10% by mass), and the like.
  • the lower limit of the content of ashless coal in the above solution is preferably 5% by mass, and more preferably 8% by mass.
  • an upper limit of content of ashless coal in the said solution 50 mass% is preferable, 40 mass% is more preferable, and 25 mass% is further more preferable. If the content of the ashless coal is less than the lower limit, the resulting porous carbon particles are excessively pulverized and the handling of the porous carbon particles may be difficult. Moreover, since the quantity of the porous carbon particles obtained from the liquid per unit quantity decreases, there exists a possibility that manufacturing efficiency may fall.
  • the content of the ashless coal exceeds the upper limit, the amount of the solvent is relatively insufficient, and undissolved ashless coal is likely to be generated, so that porous carbon particles may not be obtained. is there.
  • content of the said ashless coal can be adjusted with the quantity of coal added to a solvent by 1st mixing part S11.
  • the lower limit of the content of the polymer compound relative to the total amount of the ashless coal and the polymer compound is preferably 1% by mass, more preferably 3% by mass, and even more preferably 5% by mass.
  • the upper limit of the content of the polymer compound relative to the total amount of the ashless coal and the polymer compound is preferably 15% by mass, and more preferably 10% by mass.
  • the polymer compound may be directly dissolved in the solution, or a solution prepared by dissolving the polymer compound in a solvent is mixed with the liquid component. Also good.
  • Solid content generation step S15 the solution in which the ashless coal and the polymer compound are dissolved in the solvent is spray-dried.
  • generation process S15 can be performed by the spraying part.
  • a sprayer can be used as the spray unit.
  • this atomizer a well-known flash distiller and a cyclone can be mentioned.
  • Such a sprayer has a spray nozzle that injects a spraying gas into a solution supplied to the spraying section through a supply pipe from the separation section.
  • the spray nozzle can be configured, for example, by connecting a supply pipe to a two-fluid nozzle or a four-fluid nozzle.
  • the solution is refined and dispersed by colliding the heated atomizing gas with the solution through a spray nozzle.
  • the solvent in the mist-like solution due to the collision of the atomizing gas evaporates in a flash distiller or a cyclone by self-sensible heat and the application of heat from the heated atomizing gas.
  • the solvent is rapidly desorbed from each droplet of the atomized solution.
  • the atomized solution is dried by rapid desorption of the solvent, and a solid content mainly composed of ashless coal is obtained.
  • the solvent is released from the state where the solvent is trapped inside the carbon layer mainly composed of carbon derived from ashless coal, and this solid content is formed.
  • a carbon layer constituting the hollow portion is provided.
  • the carbon layer has a plurality of micropores induced by the desorption of the solvent.
  • an inert gas such as nitrogen as the atomizing gas. Since the inert gas has low reactivity, it has little influence on the composition of the solid content produced. Further, since it is a gas even at a relatively low temperature below the boiling point of the solvent, it is easy to separate the evaporated solvent and the spray gas.
  • the lower limit of the pressure of the spray gas (spray pressure) that collides with the solution is preferably 0.1 MPa, and more preferably 0.2 MPa.
  • the upper limit of the spray pressure is preferably 1 MPa, and more preferably 0.5 MPa.
  • the lower limit of the temperature of the spray gas is preferably 100 ° C, more preferably 150 ° C.
  • the upper limit of the temperature of the spray gas is preferably 450 ° C., more preferably 400 ° C. If the temperature of the atomizing gas is less than the lower limit, the solvent will not be sufficiently desorbed, so that micropores may not be sufficiently formed. Conversely, if the temperature of the spray gas exceeds the upper limit, the energy consumption for heating may increase unnecessarily.
  • the lower limit of the solution feeding speed of the solution supplied to the spraying part through the supply pipe from the separation part is preferably 0.5 kg / h, more preferably 0.7 kg / h.
  • the upper limit of the liquid feeding speed is preferably 2 kg / h, more preferably 1.5 kg / h.
  • the liquid feeding speed is less than the lower limit, the amount of porous carbon particles obtained per unit time is decreased, and thus production efficiency may be decreased.
  • the liquid feeding speed exceeds the upper limit, the amount of heat applied to the solution is insufficient, and the desorption of the solvent becomes insufficient, so that micropores may not be sufficiently formed.
  • the lower limit of the temperature of the solution supplied to the spraying part through the supply pipe from the separation part is preferably 60 ° C, more preferably 70 ° C, and further preferably 90 ° C.
  • an upper limit of the temperature of the said solution 160 degreeC is preferable and 150 degreeC is more preferable. If the temperature of the solution is less than the lower limit, the amount of heat applied to the solution is insufficient, and the desorption of the solvent becomes insufficient, so that micropores may not be sufficiently formed. Conversely, if the temperature of the solution exceeds the upper limit, the energy consumption for heating may increase unnecessarily.
  • the temperature of the above solution is higher than the boiling point of the solvent.
  • the lower limit of the temperature difference between the solution temperature and the boiling point of the solvent is preferably 10 ° C, more preferably 20 ° C.
  • an upper limit of the said temperature difference 50 degreeC is preferable and 40 degreeC is more preferable. If the temperature difference is less than the lower limit, the desorption of the solvent becomes insufficient, and there is a possibility that micropores are not sufficiently formed. Conversely, if the temperature difference exceeds the upper limit, the energy consumption for heating may increase unnecessarily.
  • the solid content obtained in the spraying part is naturally cooled in the spraying part and discharged at a temperature of 40 ° C. or more and 80 ° C. or less.
  • the lower limit of the average solid content is preferably 1 ⁇ m, more preferably 2 ⁇ m.
  • the upper limit of the average diameter of the solid content is preferably 20 ⁇ m and more preferably 10 ⁇ m.
  • the average diameter of the solid content is determined mainly by the size of the solution droplet sprayed in the solid content generation step S15. Since the size of the droplets of the solution to be sprayed is mainly determined by the spray pressure and the liquid feeding speed, the spray pressure and the liquid feeding speed may be adjusted so that the average diameter of the solid content is within the above range. When the average diameter of the solid content is less than the lower limit, it means that the droplet size of the solution to be sprayed is small, and the amount of the solvent desorbed from the solution is small.
  • Heating step S2 the solid content obtained in the spray drying step S1 is heated.
  • This heating process S2 can be performed by a heating part.
  • Heating part The heating unit carbonizes the solid content obtained in the spray unit. By this carbonization, porous carbon particles are obtained.
  • the heating unit for example, a known electric furnace or the like can be used. After inserting the solid content into the heating unit and replacing the inside with an inert gas, heating is performed while blowing the inert gas into the heating unit. Can carbonize solids. Although it does not specifically limit as said inert gas, For example, nitrogen, argon, etc. can be mentioned. Of these, inexpensive nitrogen is preferred.
  • the polymer compound dispersed in the solid content in the spray drying step S1 is mostly decomposed and dissipated in the heating step S2, so that it is considered that fine voids (mesopores) remain in the ashless coal. .
  • Simply mixing ashless charcoal and a polymer compound will cause phase separation between the two so that no mesopores are produced.
  • mesopores are likely to increase due to decomposition and dissipation of the polymer compound in the heating step S2.
  • the lower limit of the heating temperature is preferably 500 ° C, more preferably 700 ° C.
  • the upper limit of the heating temperature is preferably 3000 ° C and more preferably 2800 ° C. There exists a possibility that carbonization may become inadequate that the said heating temperature is less than the said minimum. Conversely, if the heating temperature exceeds the above upper limit, the production cost may increase from the viewpoint of improving the heat resistance of the equipment and fuel consumption.
  • a temperature increase rate it can be 0.01 degree-C / min or more and 10 degree-C / min or less, for example.
  • the lower limit of the heating time is preferably 10 minutes, and more preferably 20 minutes.
  • the upper limit of the heating time is preferably 10 hours, more preferably 8 hours. There exists a possibility that carbonization may become inadequate that heating temperature is less than the said minimum. Conversely, if the heating time exceeds the above upper limit, the production efficiency of the porous carbon fiber may be reduced.
  • infusibilization may be performed before carbonization. This infusibilization treatment can prevent solids from fusing together. Infusibilization is performed, for example, by heating in an atmosphere containing oxygen using a known heating furnace. As an atmosphere containing oxygen, air is generally used.
  • the lower limit of the infusibilization temperature when infusibilizing is preferably 150 ° C., more preferably 180 ° C.
  • the upper limit of the infusibilization temperature is preferably 300 ° C, and more preferably 280 ° C. If the infusibilization treatment temperature is less than the lower limit, infusibilization may be insufficient, or the infusibilization treatment time may be increased, and production efficiency may be reduced. Conversely, if the infusibilization temperature exceeds the upper limit, the solid content may melt before being infusible.
  • the lower limit of the infusibilization time is preferably 10 minutes, more preferably 20 minutes.
  • the upper limit of the infusibilization time is preferably 120 minutes, and more preferably 90 minutes. If the infusibilization time is less than the lower limit, infusibilization may be insufficient. Conversely, if the infusibilization treatment time exceeds the upper limit, the production efficiency of the porous carbon particles may be reduced.
  • a solvent containing an organic compound containing oxygen atoms or nitrogen atoms and having a boiling point at atmospheric pressure within the above range as a main component is used. Since the ashless coal and the polymer compound can be dissolved in such a solvent at a high concentration, the production efficiency can be increased. Therefore, by using the method for producing porous carbon particles, porous carbon particles having relatively high production efficiency and production cost and a large specific surface area can be produced.
  • ashless coal can be eluted into the solvent by the solvent extraction treatment of coal in the elution step S12. Therefore, the production cost of the porous carbon particles can be further reduced by using a solution in which the polymer compound is mixed with the liquid component in which the ashless coal is dissolved in the solvent.
  • the porous carbon particle includes a carbon layer containing carbon as a main component and enclosing a hollow portion, and the carbon layer has a plurality of pores.
  • the said porous carbon particle can be manufactured with the manufacturing method of the said porous carbon particle mentioned above.
  • the porous carbon particles produced by the method for producing porous carbon particles usually include a hollow portion in the carbon layer, but carbon having a recess is obtained by dividing the porous carbon particle according to the application. It can be used as porous carbon particles comprising a layer.
  • the lower limit of the specific surface area of the porous carbon particles is 200 m 2 / g, more preferably 250 m 2 / g, and even more preferably 300 m 2 / g. If the specific surface area is less than the lower limit, it may be difficult to use as the porous material.
  • the upper limit of the specific surface area is not particularly limited, but is usually about 3000 m 2 / g.
  • the specific surface area of the said porous carbon particle can be adjusted with content of ashless coal in a solution, the kind of solvent, spray conditions, etc., for example.
  • the porous carbon particles have a carbon layer that encloses the hollow portion, the pores are more likely to penetrate the carbon layer than the solid porous carbon particles, and the diameter of each pore is the distance from the surface. It is easy to make it uniform regardless. For this reason, even if it is a micro hole, a hole is maintained to a comparatively deep position from an outer surface, without a diameter being crushed in the middle. Moreover, since the said specific surface area is more than the said minimum, the said porous carbon particle is excellent in porosity.
  • the method for producing porous carbon particles mainly includes a dissolution step S3, a spray drying step S4, and a heating step S5 as shown in FIG.
  • ⁇ Dissolution process> In the dissolution step S3, ashless coal and a polymer compound are dissolved in a solvent. By this dissolution, a solution in which the ashless coal and the polymer compound are dissolved is obtained.
  • a preparation tank can be used for this dissolution.
  • the adjustment tank comprised similarly to the mixing part of 1st embodiment, for example is mentioned.
  • the above solvent is mainly composed of an organic compound containing an oxygen atom or a nitrogen atom, and examples thereof include the same solvents as those in the first embodiment.
  • the solvent has a boiling point at atmospheric pressure of 50 ° C. or higher and lower than 250 ° C.
  • Examples of the polymer compound include those similar to the first embodiment.
  • the ashless coal can be obtained, for example, by a method for producing ashless coal comprising a mixing step, an elution step, a solid-liquid separation step, and an evaporation step.
  • the mixing step in the method for producing ashless coal can be performed in the same manner as the first mixing step S11 of the first embodiment.
  • the solvent to be mixed in the mixing step is not limited to a solvent mainly containing an organic compound containing an oxygen atom or a nitrogen atom, and any solvent that dissolves coal can be used.
  • solvents include methyl naphthalene oil and naphthalene oil which are bicyclic aromatic compounds derived from coal.
  • the elution step in the method for producing ashless coal can be performed in the same manner as the elution step S12 of the first embodiment.
  • the lower limit of the temperature of the slurry after the temperature rise by the temperature raising portion in the elution step is preferably 300 ° C, and more preferably 360 ° C.
  • the upper limit of the temperature of the slurry is preferably 420 ° C., more preferably 400 ° C. If the temperature of the slurry is less than the lower limit, the bonds between the molecules constituting the coal cannot be sufficiently weakened, and the elution rate may decrease. On the contrary, when the temperature of the slurry exceeds the upper limit, the amount of heat for maintaining the temperature of the slurry becomes unnecessarily large, which may increase the production cost of the porous carbon particles.
  • the internal pressure of the said temperature rising part 1.1 MPa is preferable and 1.5 MPa is more preferable.
  • the upper limit of the internal pressure of the temperature raising part is preferably 5 MPa, and more preferably 4 MPa.
  • the internal pressure of the temperature raising part is less than the lower limit, the solvent is reduced by evaporation, and there is a possibility that coal may not be sufficiently dissolved.
  • the internal pressure of the said temperature rising part exceeds the said upper limit, there exists a possibility that the improvement effect of coal melt
  • Solid-liquid separation process The solid-liquid separation step in the ashless coal production method can be performed in the same manner as the solid-liquid separation step S13 of the first embodiment.
  • the heating temperature is preferably 420 ° C., more preferably 400 ° C. If the heating temperature is less than the lower limit, the solvent-soluble component may be reprecipitated and the separation efficiency may be reduced. Conversely, if the heating temperature exceeds the upper limit, the operating cost for heating may increase.
  • the lower limit of the pressure in the separation part is preferably 1 MPa, more preferably 1.4 MPa.
  • the upper limit of the pressure is preferably 3 MPa, more preferably 2 MPa. If the pressure is less than the lower limit, the solvent-soluble component may be reprecipitated and the separation efficiency may be reduced. Conversely, when the pressure exceeds the upper limit, the operating cost for pressurization may increase.
  • a separation method including a general distillation method or an evaporation method (spray drying method or the like) can be used.
  • a separation method including a general distillation method or an evaporation method (spray drying method or the like) can be used.
  • the content of the ashless coal and the content of the polymer compound in the solution in which the ashless coal and the polymer compound are dissolved by the above dissolution can be the same as in the first embodiment.
  • Heating step S5 the solid content obtained in the spray drying step S4 is heated.
  • This heating process S5 can be performed similarly using the apparatus similar to heating process S2 of 1st embodiment.
  • the configuration in which the mixing unit in the first mixing step has the preparation tank has been described.
  • the present invention is not limited to this configuration, and the preparation tank may be omitted as long as the solvent and coal can be mixed.
  • the preparation tank may be omitted and a line mixer may be provided between the supply pipe and the separation unit.
  • the apparatus structure used at each process is not limited to the said embodiment.
  • the method for producing ashless coal by solvent extraction has been described.
  • the method for producing ashless coal is not limited thereto, and for example, the ashless coal is produced by mixing and heating coal and a hydrogen donating solvent. Ashless charcoal can also be used.
  • Ashless coal produced by solvent extraction of bituminous coal was prepared as a carbon raw material.
  • Table 1 shows the elemental analysis values of the ashless coal. Moreover, the carbon yield of this ashless coal was 55 mass%.
  • the amount of oxygen means the amount of components other than carbon, hydrogen, nitrogen and sulfur, and is obtained by subtracting the components of carbon, hydrogen, nitrogen and sulfur from 100% by mass.
  • polymethyl methacrylate (PMMA, carbon yield 4 mass%) was prepared.
  • pyridine having a boiling point of 115 ° C. at atmospheric pressure was prepared.
  • Pyridine is an organic compound (aromatic compound) containing nitrogen.
  • the ashless coal and the polymer compound are dissolved in this solvent, and the content of the ashless coal in the solution is 10% by mass, and the content of the polymer compound with respect to the total amount of the ashless coal and the polymer compound is 2% by mass. It was prepared as follows.
  • This solution was sprayed into a cyclone using a two-fluid nozzle under the conditions of a spraying pressure of 0.3 MPa and a solution feeding speed of 1 kg / h to obtain a solid content.
  • the cyclone inlet temperature was 140 ° C. and the outlet temperature was 70 ° C.
  • the solid content was heated to 900 ° C. at a temperature rising rate of 5 ° C./min, and heat treatment (carbonization) for 30 minutes was performed to produce porous carbon particles of Example 1.
  • Example 2 Porous carbon particles were produced in the same manner as in Example 1 except that the content of ashless coal in the solution was 30% by mass.
  • Example 3 The porous carbon particles of Example 3 were the same as Example 1 except that the solvent was tetrahydrofuran (THF) having a boiling point of 66 ° C. at atmospheric pressure, the cyclone inlet temperature was 100 ° C., and the outlet temperature was 50 ° C. Manufactured. Note that THF is an organic compound (polar organic compound) containing oxygen.
  • Examples 4 and 5 are PMMA
  • Examples 6 and 7 are polyvinyl pyrrolidone (PVP, carbon yield 0% by mass)
  • Example 8 is polystyrene (PSt, carbon yield 10% by mass).
  • a solution was prepared so that the content of the molecular compound was as shown in Table 2.
  • the polymer compound was not dissolved in the solution.
  • Porous carbon particles of Examples 4 to 8 and Comparative Example 1 were produced in the same manner as Example 1 except that the above solution was used.
  • ⁇ Particle size> The particle size of the solid content was measured with an optical microscope. In the measurement, the particle diameter of each particle within the field of view of the optical microscope was measured, and the range was determined. The results are shown in Table 2.
  • porous carbon particles having a large specific surface area can be produced with relatively good production efficiency and production cost.
  • the porous carbon particle of this invention has a large specific surface area, it can be used suitably as an adsorbent or an electronic component.

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  • Chemical & Material Sciences (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
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  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
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Abstract

Le but de la présente invention est de fournir un procédé de production de particules de carbone poreux à grande surface spécifique, qui présente un excellent rendement de production et des coûts de production intéressants comparativement parlant, ainsi que des particules de carbone poreux. Ce procédé de production de particules de carbone poreux comprend une étape de séchage par pulvérisation d'une solution de charbon sans cendres et d'un composé polymère dissous dans un solvant et une étape de chauffage de la fraction de matières solides obtenue lors de l'étape de séchage par pulvérisation. Le solvant possède comme constituant principal un composé organique qui comprend un atome d'oxygène ou un atome d'azote et présente un point d'ébullition variant de 50 °C à moins de 250 °C à la pression atmosphérique. La pression de pulvérisation et la vitesse d'alimentation peuvent être modulées de façon à ce que le diamètre moyen des matières solides de la fraction de matières solides soit compris entre 1 et 20 µm. La teneur en composé polymère par rapport à la quantité totale de charbon sans cendres et de composé polymère varie, de préférence, de 1 à 15 % en masse. Ces particules de carbone poreux comprennent du carbone comme constituant principal et comportent une couche de carbone renfermant une partie creuse. La couche de carbone comporte une pluralité de pores, et la surface spécifique est égale ou supérieure à 200 cm²/g.
PCT/JP2018/002240 2017-04-07 2018-01-25 Procédé de production de particules de carbone poreux et particules de carbone poreux WO2018186003A1 (fr)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115403041A (zh) * 2022-09-15 2022-11-29 中国地质大学（北京） 一种半纤维素基中空多孔碳及其制备方法和其在锌离子储能器件中的应用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010161337A (ja) * 2008-09-29 2010-07-22 Sanwa Yushi Kk 植物焼成物及び電磁波遮蔽体
WO2016052981A1 (fr) * 2014-09-30 2016-04-07 주식회사 엘지화학 Procede de fabrication de capsules creuses de carbone
JP2017014079A (ja) * 2015-07-02 2017-01-19 株式会社神戸製鋼所 活性炭の製造方法、活性炭及び電気二重層キャパシタ用電極材料

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010161337A (ja) * 2008-09-29 2010-07-22 Sanwa Yushi Kk 植物焼成物及び電磁波遮蔽体
WO2016052981A1 (fr) * 2014-09-30 2016-04-07 주식회사 엘지화학 Procede de fabrication de capsules creuses de carbone
JP2017014079A (ja) * 2015-07-02 2017-01-19 株式会社神戸製鋼所 活性炭の製造方法、活性炭及び電気二重層キャパシタ用電極材料

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115403041A (zh) * 2022-09-15 2022-11-29 中国地质大学（北京） 一种半纤维素基中空多孔碳及其制备方法和其在锌离子储能器件中的应用
CN115403041B (zh) * 2022-09-15 2023-11-21 中国地质大学（北京） 一种半纤维素基中空多孔碳及其制备方法和其在锌离子储能器件中的应用

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