US20100325946A1 - Solid fuel and method of producing solid fuel - Google Patents
Solid fuel and method of producing solid fuel Download PDFInfo
- Publication number
- US20100325946A1 US20100325946A1 US12/918,018 US91801808A US2010325946A1 US 20100325946 A1 US20100325946 A1 US 20100325946A1 US 91801808 A US91801808 A US 91801808A US 2010325946 A1 US2010325946 A1 US 2010325946A1
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- Prior art keywords
- solid fuel
- beer lees
- rotor
- sleeve
- housing
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- ATUOYWHBWRKTHZ-UHFFFAOYSA-N CCC Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS 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
- C10L5/00—Solid fuels
- C10L5/40—Solid fuels essentially based on materials of non-mineral origin
- C10L5/44—Solid fuels essentially based on materials of non-mineral origin on vegetable substances
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
Definitions
- the present invention relates to a solid fuel which may be used in thermal power generation equipment, boilers, stone ovens, smokers, wood stoves and ascending kilns for ceramics, and a method of producing such a solid fuel.
- Firewood which is known as a solid fuel is used as a fuel for cooking and warming, and is an important fuel source in stone ovens and wood stoves for baking pizza and bread.
- firewood is used in the firing process of pottery, porcelain and brick produced by traditional techniques, and many ceramists are paying a special attention to wood to create subtle shades from firing at non-uniform temperatures.
- Living trees which serve as a material of firewood contain nearly 50% of moisture and must be dried to a moisture content of around 15% to burn them as firewood. If insufficiently dried firewood is burnt, a large amount of tar or soot may occur.
- the standards management is only directed to cut wood into the same length, and the quality is uneven and varies considerably from firewood to firewood. Flame regulation is therefore difficult.
- sawdust is used as a material to be formed into a firewood shape and is employed as a fuel. Flame can be easily regulated when sawdust is used as firewood because the moisture is controlled during the processing and firewood of the same size can be industrially produced. Firewood obtained from a sawdust material is also a recycled product.
- sawdust is originally obtained from living trees and is therefore a resource only obtained after cutting trees useful for reducing CO 2 emissions. In addition, burning causes the volatile components inherent in living trees to generate disagreeable eye-smarting smoke. It is expensive only to collect enough sawdust to distribute as firewood. Sawdust is considerably distinct from beer lees which are wastes generated in large amounts in beer factories.
- Patent Document 1 discloses a forming device for carbonizing beer lees, but it is clear that the beer lees formed by the forming device is a carbonaceous material, is less flammable and is therefore not a good solid fuel. In other words, it is clear that this type of carbonaceous material is excellent in the function of adhering an adsorbent or microorganism thereto and growing the adhered adsorbent or microorganism (see Non-Patent Document 1), but has low burning performance.
- Patent Document 1 JP 2000-33496 A
- Non-Patent Document 1 Search on the Internet, Oct. 30, 2008; [http://www.japan-hp.com/ksd_hako.html]
- the solid fuel of the present invention is characterized by the inclusion of particulate beer lees heat-treated while preventing carbonization.
- This solid fuel can be prepared by heating beer lees under agitation and compression-molding the agitated beer lees under heating into a solid fuel shape.
- the present invention can provide a solid fuel which has excellent burning characteristics and may be substituted for firewood obtained by drying living trees.
- the present invention is characterized in that beer lees are used as a solid fuel material.
- the usage of living trees that have been used as a material of a solid fuel (firewood) is greatly limited in terms of CO 2 reduction, and a sufficient amount of sawdust to distribute it as firewood cannot be obtained from a living tree material.
- Beer factories producing beer which is a universal beverage are constructed all over the world. Therefore, a large amount of beer lees can be obtained everyday even from one beer factory, which enables transportation costs and CO 2 emissions resulting from transportation to be considerably reduced. Beer lees are considerably distinct from petroleum which is produced only in some areas including the Middle East and involves transportation for its supply.
- the solid fuel made from beer lees has thus a lot of more excellent properties than conventional energy sources. As will be described later, the solid fuel made from beer lees has more excellent burning performance than that made from living trees and may be a substitute for the latter.
- FIG. 1 is a schematic view of a solid fuel production device for effectively implementing the production method.
- FIG. 2 is a cross-sectional view of an agitation and molding portion making up part of the solid fuel production device.
- FIG. 3 is an exploded perspective view of the agitation and molding portion.
- a hopper portion 20 is of a tapered shape in which the diameter size gradually decreases toward the bottom side and is connected to an inlet 11 a formed in a housing body 11 of an agitation and molding portion 10 .
- the housing body 11 of the agitation and molding portion 10 is formed in a cylindrical shape and a hemispherical edge housing 12 is fixed via fixing bolts 13 to one end of the housing body 11 in the horizontal direction (X-axis direction).
- a plurality of (ten in this embodiment) inner blades 12 a having a helix angle are formed at the inner surface of the edge housing 12 and a discharge port 12 b for discharging beer lees is formed at the distal end of the edge housing 12 .
- the proximal end of the edge housing 12 is fixed via fixing bolts 19 to the housing body 11 .
- a rotor 14 is rotatably accommodated in the edge housing 12 and outer blades 14 a having a helix angle are formed at the outer surface of the rotor 14 .
- the outer blades 14 a of the rotor 14 are twisted in the opposite direction with respect to the inner blades 12 a of the edge housing 12 .
- a rotating shaft 14 b of the rotor 14 extends in the X-axis direction and is driven to rotate by the driving force transmitted from a motor 40 shown in FIG. 1 .
- the drive mechanism of the rotor 14 is described later.
- a sleeve 15 is formed in a cylindrical shape and extends in the X-axis direction. One end of the sleeve 15 in the X-axis direction is fixed to a flange portion 18 secured to the distal end of the edge housing 12 .
- An edge screw 16 which extends inside the sleeve portion 15 is attached to one end of the rotor 14 in the X-axis direction.
- a screw shaft 16 a of the edge screw 16 is disposed coaxially with the rotating shaft 14 b of the rotor 14 , and the drive force transmitted from the motor 40 causes the rotor 14 and the edge screw 16 to integrally rotate.
- R 1 and R 2 When the internal diameter of the sleeve 15 and the external diameter of the screw shaft 16 a are represented by R 1 and R 2 , respectively, R 1 -R 2 is preferably from 0.3 to 0.5 mm and more preferably 0.3 mm.
- a heat generating cylinder 17 is disposed concentrically with the sleeve 15 on the outer peripheral surface of the sleeve 15 . Heat transmitted from a heat source (not shown) causes the heat generating cylinder 17 to generate heat.
- a gear box 30 includes a first gear 31 and a second gear line 32 meshed with the first gear 31 .
- the second gear line 32 is connected to the rotating shaft 14 b of the rotor 14 and the rotor 14 rotates in response to the rotational operation of the second gear line 32 .
- An output gear 42 is attached to an output shaft 41 of the motor 40 and is connected to the first gear 31 accommodated in the gear box 30 . Therefore, once the motor 40 is driven, the drive force can be transmitted to the output gear 42 , the first gear 31 and the second gear line 32 in this order to rotate the rotor 14 .
- the first step for producing beer includes crushing a malt which is a germinate barley material, boiling the crushed malted barley to obtain mash and extracting wort from the mash. This step is called mashing. In this step, wort is extracted to generate residues, which are generally called “beer lees.”
- the beer lees usually contain 60 to 75% of moisture and are dried or dehydrated to a moisture content of 1 to 15% before being charged into the housing 11 through the hopper 20 .
- the upper limit is set to 15% because at a moisture content in excess of 15%, a large amount of moisture vapor is generated from the beer lees during the heating to excessively increase the internal pressure of the housing 11 .
- the lower limit is set to 1% because at a moisture content of less than 1%, the compression-molded beer lees do not easily agglomerate and cannot be used as a solid fuel.
- the dried beer lees are charged into the housing body 11 through the hopper 20 .
- the feed rate of the beer lees to the housing body 11 is preferably at least 100 kg/h and more preferably at least 130 kg/h.
- the solid fuel positioned inside the sleeve 15 is heated for a long time to carbonize the solid fuel surface.
- the feed rate of the beer lees may be suitably changed according to the device configuration of the production device from the viewpoint that the solid fuel surface should not be carbonized.
- the beer lees fed to the housing body 11 is transferred to the discharge port 12 b of the edge housing 12 through a gap formed between the rotor 14 and the edge housing 12 .
- the particulate beer lees are brought into contact with each other to generate frictional heat, thus increasing the temperature of the beer lees.
- the rotor 14 Since the rotor 14 has the plurality of outer blades 14 a formed at the outer surface thereof, the amount of beer lees transferred per revolution of the rotor 14 can be increased. On the other hand, the amount of beer lees fed from the edge housing 12 to the sleeve 15 can be limited by setting the internal diameter R 1 of the sleeve 15 and the external diameter R 2 of the screw shaft 16 a as described above.
- Enough frictional heat can be thus applied to the beer lees transferred within the edge housing 12 .
- the temperature of the beer lees can be increased to a material temperature suitable for molding at the discharge port 12 a of the edge housing 12 .
- the material temperature suitable for molding of the beer lees is approximately 90° C. or more.
- the beer lees discharged from the discharge port 12 a of the edge housing 12 are pushed into the sleeve 15 by the rotary action of the screw 16 .
- the temperature at which the sleeve 15 is heated by the heat generating cylinder 17 is preferably from 250° C. to 330° C. (390° C. at the time of preheating). At a heating temperature of less than 250° C., the solid fuel surface is increasingly cracked and the solid fuel is liable to break. At a heating temperature exceeding 330° C., a burnt thin (carbide) film is formed at the solid fuel surface.
- the heating temperature of the sleeve 15 may be suitably changed according to the device configuration of the solid fuel production device. In this case, cracks generated in the solid fuel and a burnt thin film formed at the surface can be visually identified. Therefore, the optimal heating temperature can be empirically derived by adjusting the heating temperature of the sleeve 15 while visually observing the surface of the solid fuel discharged from the sleeve 15 .
- the beer lees within the sleeve 15 are compressed while contacting the inner surface of the sleeve 15 and the outer surface of the screw shaft 16 a of the screw 16 , transferred inside the sleeve 15 and discharged as a solid fuel.
- particulate beer lees generated as a by-product during the production of beer can be used as a material to produce a solid fuel which is eco-friendly, has stable qualities, enables easy flame regulation and satisfies the industrial standards. Since the solid fuel is obtained only by agitating, heating and compressing the beer lees, the production process can be simplified. Moreover, the evolution of fire sparks or eye-smarting smoke can be avoided. Furthermore, it is possible to provide a sensorily favorable solid fuel releasing a spicy savor of barley.
- the solid fuel may be flavored by charging into the agitation and molding portion 10 roasted coffee bean residues, particles obtained by pulverizing disused brewing barrels (e.g., sake barrel, wine barrel and whiskey barrel), residues after squeezing fruits (e.g., apple and mandarin orange), and hop residues after beer brewing in addition to the above-described beer lees.
- roasted coffee bean residues particles obtained by pulverizing disused brewing barrels (e.g., sake barrel, wine barrel and whiskey barrel), residues after squeezing fruits (e.g., apple and mandarin orange), and hop residues after beer brewing in addition to the above-described beer lees.
- Solid fuel A made from beer lees whose surfaces are not carbonized (hereinafter referred to as “Example”) and Solid fuel B made from a barrel material (hereinafter referred to as “Comparative Example”) were respectively subjected to fuel combustion experiments and compared with each other. More specifically, the flash point, the calorific power, the IMO burning velocity and the volatile components were determined to evaluate the fuel performance.
- a barrel material was used in Comparative Example. Firewood made from a barrel material is widely available in the market, can be easily purchased, and is therefore optimal to use as a comparative example for evaluating the burning characteristics of the solid fuel made from beer lees.
- the flash point was measured according to the manual for conducting tests for verifying hazardous substances under the Fire Service Act. More specifically, a closed-cup flash point tester was used as the flash point measuring instrument. The test was conducted in the Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd. The test conditions of Example included a temperature of 26° C., a humidity of 58% and an atmospheric pressure of 1008 hPa. The test was conducted on Aug. 27, 2008. The test conditions of Comparative Example included a temperature of 24° C., a humidity of 51% and an atmospheric pressure of 1010 hPa. The test was conducted on Aug. 25, 2008. The test results of Example were shown in Table 1 and those of Comparative Example were shown in Table 2.
- Example and Comparative Example were 217° C. and 246° C., respectively, which showed that the solid fuel in Example has a lower flash point and more readily catch fire than the solid fuel in Comparative Example.
- the calorific power was measured according to the JIS M 8814 manual.
- the test was conducted in the Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd.
- the test conditions included a temperature of 22° C., a humidity of 78% and an atmospheric pressure of 1007 hPa.
- the test results of Example were shown in Table 3 and those of Comparative Example were shown in Table 4.
- the calorific power in Example and that in Comparative Example were 19940 J/g and 18540 J/g, respectively, which showed that the calorific power in Example is better than that in Comparative Example.
- the IMO burning velocity was measured in the Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd.
- the test conditions included a temperature of 27° C. and a humidity of 84%.
- the following criteria were applied to the evaluation method. More specifically, a case in which the burning velocity was 2.0 mm/sec or more was rated as having high flammability hazard, a case in which the burning velocity was higher than 0 mm/sec but less than 2.0 mm/sec was rated as having medium flammability hazard, and a case in which the burning velocity was 0 mm/sec was rated as having low flammability hazard.
- a prism-shaped specimen with a total length of 250 mm, a width of 20 mm and a height of 10 mm was deposited on a heat insulation plate (with a thickness of 10 mm and a thermal conductivity at 0° C. of up to 0.1 W/m ⁇ K) and one end of the specimen was fired by using a firing device for liquefied petroleum gas. The period of time it took for burning to further proceed over a length of 100 mm from the area of 120 mm where the reaction had previously taken place was measured. The test was repeated six times in both of Example and Comparative Example. The test results of Example are shown in Table 5 and those of Comparative Example are shown in Table 6.
- Burning Flammability Time required to burn length of velocity hazard No. 100 mm (sec) (mm/sec) (reference) 1 Burning does not continue 0 low 2 Burning does not continue 0 low 3 Burning does not continue 0 low 4 Burning does not continue 0 low 5 Burning does not continue 0 low 6 Burning does not continue 0 low Average Burning does not continue 0 low
- Example had a lower burning velocity and therefore a lower flammability hazard than Comparative Example. In other words, it was revealed that the fuel in Example burns longer, is more safe and is easier in handling than that in Comparative Example.
- Example and Comparative Example were burnt in a burning device JIS K 7217. Gases generated during the burning were collected in a Tedlar bag and the collected gases were determined by gas chromatography (GC/TCD).
- the combustion gas generator used was PCT-1 available from Sugiyama-Gen Co., Ltd. The temperature was set to 750° C. Air was used for the combustion supporting gas. The combustion supporting gas was fed at a feed rate of 0.5 L/min.
- the gas chromatograph used was GC-14B available from Shimadzu Corporation.
- Table 7 shows data of Example, and the vertical axis and horizontal axis represent component amount and time, respectively.
- Table 8 shows data of Comparative Example, and the vertical axis and horizontal axis represent component amount and time, respectively.
- FIG. 1 is a schematic view of a solid fuel production device for effectively implementing the production method.
- FIG. 2 is a cross-sectional view of an agitation and molding portion making up part of the solid fuel production device.
- FIG. 3 is an exploded perspective view of the agitation and molding portion.
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Abstract
Description
- The present invention relates to a solid fuel which may be used in thermal power generation equipment, boilers, stone ovens, smokers, wood stoves and ascending kilns for ceramics, and a method of producing such a solid fuel.
- Firewood which is known as a solid fuel is used as a fuel for cooking and warming, and is an important fuel source in stone ovens and wood stoves for baking pizza and bread.
- In the ceramic industry, firewood is used in the firing process of pottery, porcelain and brick produced by traditional techniques, and many ceramists are paying a special attention to wood to create subtle shades from firing at non-uniform temperatures.
- Living trees which are used as a material of firewood absorb carbon dioxide and release oxygen in the photosynthesis and are therefore an extremely important natural resource to protect the global environment. Accordingly, use of firewood made from living trees should be avoided as much as possible.
- Living trees which serve as a material of firewood contain nearly 50% of moisture and must be dried to a moisture content of around 15% to burn them as firewood. If insufficiently dried firewood is burnt, a large amount of tar or soot may occur. The standards management is only directed to cut wood into the same length, and the quality is uneven and varies considerably from firewood to firewood. Flame regulation is therefore difficult.
- On the other hand, there is also a method in which sawdust is used as a material to be formed into a firewood shape and is employed as a fuel. Flame can be easily regulated when sawdust is used as firewood because the moisture is controlled during the processing and firewood of the same size can be industrially produced. Firewood obtained from a sawdust material is also a recycled product. However, sawdust is originally obtained from living trees and is therefore a resource only obtained after cutting trees useful for reducing CO2 emissions. In addition, burning causes the volatile components inherent in living trees to generate disagreeable eye-smarting smoke. It is expensive only to collect enough sawdust to distribute as firewood. Sawdust is considerably distinct from beer lees which are wastes generated in large amounts in beer factories.
- Patent Document 1 discloses a forming device for carbonizing beer lees, but it is clear that the beer lees formed by the forming device is a carbonaceous material, is less flammable and is therefore not a good solid fuel. In other words, it is clear that this type of carbonaceous material is excellent in the function of adhering an adsorbent or microorganism thereto and growing the adhered adsorbent or microorganism (see Non-Patent Document 1), but has low burning performance.
- Non-Patent Document 1: Search on the Internet, Oct. 30, 2008; [http://www.japan-hp.com/ksd_hako.html]
- Accordingly, it has been required to develop a solid fuel that may be used as a substitute fuel for living trees, coal, petroleum and the like.
- In order to solve the above-described problems, the solid fuel of the present invention is characterized by the inclusion of particulate beer lees heat-treated while preventing carbonization. This solid fuel can be prepared by heating beer lees under agitation and compression-molding the agitated beer lees under heating into a solid fuel shape.
- The present invention can provide a solid fuel which has excellent burning characteristics and may be substituted for firewood obtained by drying living trees.
- The present invention is characterized in that beer lees are used as a solid fuel material. The usage of living trees that have been used as a material of a solid fuel (firewood) is greatly limited in terms of CO2 reduction, and a sufficient amount of sawdust to distribute it as firewood cannot be obtained from a living tree material.
- In contrast, beer lees are wastes from the production of beer. Beer factories producing beer which is a universal beverage are constructed all over the world. Therefore, a large amount of beer lees can be obtained everyday even from one beer factory, which enables transportation costs and CO2 emissions resulting from transportation to be considerably reduced. Beer lees are considerably distinct from petroleum which is produced only in some areas including the Middle East and involves transportation for its supply.
- In addition, in cold regions, every home may often have at least one fireplace for burning firewood. Therefore, a solid fuel made from beer lees can be directly put in the fireplace and burnt to keep warm. Therefore, it is not necessary to convert energy obtained from burning into electric power, which enables infrastructural problems to be reduced. Beer lees are also considerably distinct from fuel cells which require hydrogen filling stations.
- The solid fuel made from beer lees has thus a lot of more excellent properties than conventional energy sources. As will be described later, the solid fuel made from beer lees has more excellent burning performance than that made from living trees and may be a substitute for the latter.
- A method of producing a solid fuel made from beer lees is described below in detail.
- The solid fuel production method of the present invention is first described by reference to
FIGS. 1 , 2 and 3.FIG. 1 is a schematic view of a solid fuel production device for effectively implementing the production method.FIG. 2 is a cross-sectional view of an agitation and molding portion making up part of the solid fuel production device.FIG. 3 is an exploded perspective view of the agitation and molding portion. - Now referring to these drawings, a
hopper portion 20 is of a tapered shape in which the diameter size gradually decreases toward the bottom side and is connected to aninlet 11 a formed in ahousing body 11 of an agitation andmolding portion 10. - As shown in
FIG. 2 , thehousing body 11 of the agitation andmolding portion 10 is formed in a cylindrical shape and ahemispherical edge housing 12 is fixed viafixing bolts 13 to one end of thehousing body 11 in the horizontal direction (X-axis direction). - A plurality of (ten in this embodiment)
inner blades 12 a having a helix angle are formed at the inner surface of theedge housing 12 and adischarge port 12 b for discharging beer lees is formed at the distal end of theedge housing 12. The proximal end of theedge housing 12 is fixed viafixing bolts 19 to thehousing body 11. - A
rotor 14 is rotatably accommodated in theedge housing 12 andouter blades 14 a having a helix angle are formed at the outer surface of therotor 14. Theouter blades 14 a of therotor 14 are twisted in the opposite direction with respect to theinner blades 12 a of theedge housing 12. - A rotating
shaft 14 b of therotor 14 extends in the X-axis direction and is driven to rotate by the driving force transmitted from amotor 40 shown inFIG. 1 . The drive mechanism of therotor 14 is described later. - A
sleeve 15 is formed in a cylindrical shape and extends in the X-axis direction. One end of thesleeve 15 in the X-axis direction is fixed to aflange portion 18 secured to the distal end of theedge housing 12. - An
edge screw 16 which extends inside thesleeve portion 15 is attached to one end of therotor 14 in the X-axis direction. - A
screw shaft 16 a of theedge screw 16 is disposed coaxially with the rotatingshaft 14 b of therotor 14, and the drive force transmitted from themotor 40 causes therotor 14 and theedge screw 16 to integrally rotate. - When the internal diameter of the
sleeve 15 and the external diameter of thescrew shaft 16 a are represented by R1 and R2, respectively, R1-R2 is preferably from 0.3 to 0.5 mm and more preferably 0.3 mm. Aheat generating cylinder 17 is disposed concentrically with thesleeve 15 on the outer peripheral surface of thesleeve 15. Heat transmitted from a heat source (not shown) causes theheat generating cylinder 17 to generate heat. - As shown in
FIG. 1 , agear box 30 includes afirst gear 31 and asecond gear line 32 meshed with thefirst gear 31. Thesecond gear line 32 is connected to the rotatingshaft 14 b of therotor 14 and therotor 14 rotates in response to the rotational operation of thesecond gear line 32. - An
output gear 42 is attached to anoutput shaft 41 of themotor 40 and is connected to thefirst gear 31 accommodated in thegear box 30. Therefore, once themotor 40 is driven, the drive force can be transmitted to theoutput gear 42, thefirst gear 31 and thesecond gear line 32 in this order to rotate therotor 14. - Next, the solid fuel production method using the above-described production device is described. The first step for producing beer includes crushing a malt which is a germinate barley material, boiling the crushed malted barley to obtain mash and extracting wort from the mash. This step is called mashing. In this step, wort is extracted to generate residues, which are generally called “beer lees.”
- The beer lees usually contain 60 to 75% of moisture and are dried or dehydrated to a moisture content of 1 to 15% before being charged into the
housing 11 through thehopper 20. The upper limit is set to 15% because at a moisture content in excess of 15%, a large amount of moisture vapor is generated from the beer lees during the heating to excessively increase the internal pressure of thehousing 11. The lower limit is set to 1% because at a moisture content of less than 1%, the compression-molded beer lees do not easily agglomerate and cannot be used as a solid fuel. - The dried beer lees are charged into the
housing body 11 through thehopper 20. The feed rate of the beer lees to thehousing body 11 is preferably at least 100 kg/h and more preferably at least 130 kg/h. At a feed rate of 100 kg/h or less, the solid fuel positioned inside thesleeve 15 is heated for a long time to carbonize the solid fuel surface. The feed rate of the beer lees may be suitably changed according to the device configuration of the production device from the viewpoint that the solid fuel surface should not be carbonized. - By the rotary action of the
rotor 14, the beer lees fed to thehousing body 11 is transferred to thedischarge port 12 b of theedge housing 12 through a gap formed between therotor 14 and theedge housing 12. In this process, the particulate beer lees are brought into contact with each other to generate frictional heat, thus increasing the temperature of the beer lees. - Since the
rotor 14 has the plurality ofouter blades 14 a formed at the outer surface thereof, the amount of beer lees transferred per revolution of therotor 14 can be increased. On the other hand, the amount of beer lees fed from theedge housing 12 to thesleeve 15 can be limited by setting the internal diameter R1 of thesleeve 15 and the external diameter R2 of thescrew shaft 16 a as described above. - Enough frictional heat can be thus applied to the beer lees transferred within the
edge housing 12. As a result, the temperature of the beer lees can be increased to a material temperature suitable for molding at thedischarge port 12 a of theedge housing 12. The material temperature suitable for molding of the beer lees is approximately 90° C. or more. - The beer lees discharged from the
discharge port 12 a of theedge housing 12 are pushed into thesleeve 15 by the rotary action of thescrew 16. The temperature at which thesleeve 15 is heated by theheat generating cylinder 17 is preferably from 250° C. to 330° C. (390° C. at the time of preheating). At a heating temperature of less than 250° C., the solid fuel surface is increasingly cracked and the solid fuel is liable to break. At a heating temperature exceeding 330° C., a burnt thin (carbide) film is formed at the solid fuel surface. - The heating temperature of the
sleeve 15 may be suitably changed according to the device configuration of the solid fuel production device. In this case, cracks generated in the solid fuel and a burnt thin film formed at the surface can be visually identified. Therefore, the optimal heating temperature can be empirically derived by adjusting the heating temperature of thesleeve 15 while visually observing the surface of the solid fuel discharged from thesleeve 15. - By the pushing action of the
screw 16 into thesleeve 15, the beer lees within thesleeve 15 are compressed while contacting the inner surface of thesleeve 15 and the outer surface of thescrew shaft 16 a of thescrew 16, transferred inside thesleeve 15 and discharged as a solid fuel. - As described above, particulate beer lees generated as a by-product during the production of beer can be used as a material to produce a solid fuel which is eco-friendly, has stable qualities, enables easy flame regulation and satisfies the industrial standards. Since the solid fuel is obtained only by agitating, heating and compressing the beer lees, the production process can be simplified. Moreover, the evolution of fire sparks or eye-smarting smoke can be avoided. Furthermore, it is possible to provide a sensorily favorable solid fuel releasing a spicy savor of barley.
- The solid fuel may be flavored by charging into the agitation and
molding portion 10 roasted coffee bean residues, particles obtained by pulverizing disused brewing barrels (e.g., sake barrel, wine barrel and whiskey barrel), residues after squeezing fruits (e.g., apple and mandarin orange), and hop residues after beer brewing in addition to the above-described beer lees. - The present invention is described more specifically by way of examples.
- Solid fuel A made from beer lees whose surfaces are not carbonized (hereinafter referred to as “Example”) and Solid fuel B made from a barrel material (hereinafter referred to as “Comparative Example”) were respectively subjected to fuel combustion experiments and compared with each other. More specifically, the flash point, the calorific power, the IMO burning velocity and the volatile components were determined to evaluate the fuel performance. A barrel material was used in Comparative Example. Firewood made from a barrel material is widely available in the market, can be easily purchased, and is therefore optimal to use as a comparative example for evaluating the burning characteristics of the solid fuel made from beer lees.
- The flash point was measured according to the manual for conducting tests for verifying hazardous substances under the Fire Service Act. More specifically, a closed-cup flash point tester was used as the flash point measuring instrument. The test was conducted in the Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd. The test conditions of Example included a temperature of 26° C., a humidity of 58% and an atmospheric pressure of 1008 hPa. The test was conducted on Aug. 27, 2008. The test conditions of Comparative Example included a temperature of 24° C., a humidity of 51% and an atmospheric pressure of 1010 hPa. The test was conducted on Aug. 25, 2008. The test results of Example were shown in Table 1 and those of Comparative Example were shown in Table 2.
-
TABLE 1 Test name Test for measuring flash point Flash point measuring Closed-cup flash point tester instrument Date of test Aug. 27, 2008 Place of test Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd. Test conditions Temperature (26° C.), humidity (58%), atmospheric pressure (1008 hPa) Flash point 217° C. -
TABLE 2 Test name Test for measuring flash point Flash point measuring Closed-cup flash point tester instrument Date of test Aug. 25, 2008 Place of test Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd. Test conditions Temperature (24° C.), humidity (51%), atmospheric pressure (1010 hPa) Flash point 246° C. - The flash point in Example and that in Comparative Example were 217° C. and 246° C., respectively, which showed that the solid fuel in Example has a lower flash point and more readily catch fire than the solid fuel in Comparative Example.
- The calorific power was measured according to the JIS M 8814 manual. The test was conducted in the Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd. The test conditions included a temperature of 22° C., a humidity of 78% and an atmospheric pressure of 1007 hPa. The test results of Example were shown in Table 3 and those of Comparative Example were shown in Table 4.
-
TABLE 3 Test name Measurement of heat value (total calorific power) Measurement method JIS M 8814 Date of test Aug. 27, 2008 Place of test Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd. Test conditions Temperature (22° C.), humidity (78%), atmospheric pressure (1007 hPa) Measurement result 19940 J/g -
TABLE 4 Test name Measurement of heat value (total calorific power) Measurement method JIS M 8814 Date of test Aug. 27, 2008 Place of test Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd. Test conditions Temperature (22° C.), humidity (78%), atmospheric pressure (1007 hPa) Measurement result 18540 J/g - The calorific power in Example and that in Comparative Example were 19940 J/g and 18540 J/g, respectively, which showed that the calorific power in Example is better than that in Comparative Example.
- The IMO burning velocity was measured in the Safety Engineering Laboratory, Ehime Office of Sumika Chemical Analysis Service, Ltd. The test conditions included a temperature of 27° C. and a humidity of 84%. The following criteria were applied to the evaluation method. More specifically, a case in which the burning velocity was 2.0 mm/sec or more was rated as having high flammability hazard, a case in which the burning velocity was higher than 0 mm/sec but less than 2.0 mm/sec was rated as having medium flammability hazard, and a case in which the burning velocity was 0 mm/sec was rated as having low flammability hazard. A prism-shaped specimen with a total length of 250 mm, a width of 20 mm and a height of 10 mm was deposited on a heat insulation plate (with a thickness of 10 mm and a thermal conductivity at 0° C. of up to 0.1 W/m·K) and one end of the specimen was fired by using a firing device for liquefied petroleum gas. The period of time it took for burning to further proceed over a length of 100 mm from the area of 120 mm where the reaction had previously taken place was measured. The test was repeated six times in both of Example and Comparative Example. The test results of Example are shown in Table 5 and those of Comparative Example are shown in Table 6.
-
TABLE 5 Burning Flammability Time required to burn length of velocity hazard No. 100 mm (sec) (mm/sec) (reference) 1 Burning does not continue 0 low 2 Burning does not continue 0 low 3 Burning does not continue 0 low 4 Burning does not continue 0 low 5 Burning does not continue 0 low 6 Burning does not continue 0 low Average Burning does not continue 0 low -
TABLE 6 Burning Flammability Time required to burn length of velocity hazard No. 100 mm (sec) (mm/sec) (reference) 1 1665 0.06 medium 2 1658 0.06 medium 3 1685 0.06 medium 4 1697 0.06 medium 5 1641 0.06 medium 6 1683 0.06 medium Average 1672 0.06 medium - It was revealed that Example had a lower burning velocity and therefore a lower flammability hazard than Comparative Example. In other words, it was revealed that the fuel in Example burns longer, is more safe and is easier in handling than that in Comparative Example.
- The solid fuels in Example and Comparative Example were burnt in a burning device JIS K 7217. Gases generated during the burning were collected in a Tedlar bag and the collected gases were determined by gas chromatography (GC/TCD). The combustion gas generator used was PCT-1 available from Sugiyama-Gen Co., Ltd. The temperature was set to 750° C. Air was used for the combustion supporting gas. The combustion supporting gas was fed at a feed rate of 0.5 L/min. The gas chromatograph used was GC-14B available from Shimadzu Corporation. The analysis results are shown in Tables 7 and 8. Table 7 shows data of Example, and the vertical axis and horizontal axis represent component amount and time, respectively. Table 8 shows data of Comparative Example, and the vertical axis and horizontal axis represent component amount and time, respectively.
- As for aldehyde and phenol derivatives, no component peak was found in Example, whereas remarkable peaks were detected in Comparative Example. Aldehyde and phenol derivatives are components that may irritate eyes. These results revealed that Solid fuel A has better burning performance than Solid fuel B.
-
FIG. 1 is a schematic view of a solid fuel production device for effectively implementing the production method. -
FIG. 2 is a cross-sectional view of an agitation and molding portion making up part of the solid fuel production device. -
FIG. 3 is an exploded perspective view of the agitation and molding portion. -
- 10 agitation and molding portion
- 11 housing body
- 12 edge housing
- 13 fixing bolt
- 14 rotor
- 15 sleeve
- 16 edge screw
Claims (3)
Applications Claiming Priority (3)
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JP2008035984 | 2008-02-18 | ||
JP2008-035984 | 2008-02-18 | ||
PCT/JP2008/069952 WO2009104311A1 (en) | 2008-02-18 | 2008-10-31 | Solid fuel and method of producing solid fuel |
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US20100325946A1 true US20100325946A1 (en) | 2010-12-30 |
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US12/918,018 Abandoned US20100325946A1 (en) | 2008-02-18 | 2008-10-31 | Solid fuel and method of producing solid fuel |
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US (1) | US20100325946A1 (en) |
EP (1) | EP2258816A4 (en) |
JP (1) | JP4465411B2 (en) |
CN (1) | CN101970620A (en) |
WO (1) | WO2009104311A1 (en) |
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CN102191097B (en) * | 2010-04-09 | 2013-08-14 | 神华集团有限责任公司 | Method for producing bio-briquettes |
CN102041125A (en) * | 2011-01-17 | 2011-05-04 | 泸州品创科技有限公司 | Fuel bar and preparation method thereof |
CN102206527B (en) * | 2011-05-04 | 2013-08-21 | 邹属民 | Biomass fuel and preparation method thereof |
JP5530042B1 (en) * | 2014-01-08 | 2014-06-25 | 新日鉄住金エンジニアリング株式会社 | Carbide manufacturing method and carbide manufacturing system |
RU2634645C2 (en) * | 2014-11-19 | 2017-11-02 | Татьяна Евгеньевна Белькова | Method and device for drying of firewood |
CN106957771A (en) * | 2017-05-19 | 2017-07-18 | 贵州省仁怀市茅台镇郑氏酒业有限公司 | The brewage process of Maotai-flavor liquor |
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US4863488A (en) * | 1986-06-13 | 1989-09-05 | Ube Industries, Ltd. | Solid fuels |
JPH08163977A (en) * | 1994-12-15 | 1996-06-25 | Kitagawa Iron Works Co Ltd | Carrier for decomposing organic material such as leftover food |
JP2001009317A (en) * | 1999-07-02 | 2001-01-16 | Yamamoto Co Ltd | Pulverizer |
JP2001240864A (en) * | 2000-02-28 | 2001-09-04 | Asahi Breweries Ltd | Beer lees carbonization treatment system |
US20020073612A1 (en) * | 2000-12-14 | 2002-06-20 | Takeji Motai | Artificial charcoal |
JP2004223347A (en) * | 2003-01-21 | 2004-08-12 | Kitagawa Iron Works Co Ltd | Compression pulverization apparatus |
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DE3346378A1 (en) * | 1983-12-19 | 1985-04-04 | Manger, Karlheinz | Recycling process: wine yeast (natural product) compressed by high pressure with removal of moisture, to be used as an alternative fuel in place of coal, briquettes and oil |
AT404253B (en) * | 1996-11-20 | 1998-10-27 | Steirerbrau Ag | METHOD FOR THE THERMAL RECYCLING OF TREASURES |
JP3734368B2 (en) | 1998-07-21 | 2006-01-11 | アサヒビール株式会社 | Molding equipment for beer lees carbonization |
JP3669890B2 (en) * | 2000-02-28 | 2005-07-13 | アサヒビール株式会社 | Two-stage continuous fluidized drying system for beer lees |
JP2005140484A (en) * | 2003-11-04 | 2005-06-02 | Yasunobu Yoshida | Method for circulation type drying and pulverizing fuel system of waste, and device therefor |
-
2008
- 2008-10-31 US US12/918,018 patent/US20100325946A1/en not_active Abandoned
- 2008-10-31 EP EP08872724A patent/EP2258816A4/en not_active Withdrawn
- 2008-10-31 WO PCT/JP2008/069952 patent/WO2009104311A1/en active Application Filing
- 2008-10-31 JP JP2009519076A patent/JP4465411B2/en not_active Expired - Fee Related
- 2008-10-31 CN CN2008801273032A patent/CN101970620A/en active Pending
Patent Citations (6)
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US4863488A (en) * | 1986-06-13 | 1989-09-05 | Ube Industries, Ltd. | Solid fuels |
JPH08163977A (en) * | 1994-12-15 | 1996-06-25 | Kitagawa Iron Works Co Ltd | Carrier for decomposing organic material such as leftover food |
JP2001009317A (en) * | 1999-07-02 | 2001-01-16 | Yamamoto Co Ltd | Pulverizer |
JP2001240864A (en) * | 2000-02-28 | 2001-09-04 | Asahi Breweries Ltd | Beer lees carbonization treatment system |
US20020073612A1 (en) * | 2000-12-14 | 2002-06-20 | Takeji Motai | Artificial charcoal |
JP2004223347A (en) * | 2003-01-21 | 2004-08-12 | Kitagawa Iron Works Co Ltd | Compression pulverization apparatus |
Non-Patent Citations (2)
Title |
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English abstract and machine translation for JP 08-163977 A (06-1996). * |
English abstract and machine translation for JP 2004-223347 A (08-2004). * |
Also Published As
Publication number | Publication date |
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JPWO2009104311A1 (en) | 2011-06-16 |
WO2009104311A1 (en) | 2009-08-27 |
EP2258816A1 (en) | 2010-12-08 |
JP4465411B2 (en) | 2010-05-19 |
EP2258816A4 (en) | 2012-01-25 |
CN101970620A (en) | 2011-02-09 |
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