CA2700104A1 - Pyrolysis of biomass - Google Patents
Pyrolysis of biomass Download PDFInfo
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- CA2700104A1 CA2700104A1 CA2700104A CA2700104A CA2700104A1 CA 2700104 A1 CA2700104 A1 CA 2700104A1 CA 2700104 A CA2700104 A CA 2700104A CA 2700104 A CA2700104 A CA 2700104A CA 2700104 A1 CA2700104 A1 CA 2700104A1
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- biomass material
- pyrolysis
- biomass
- vessel
- processing
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- 239000002028 Biomass Substances 0.000 title claims abstract description 53
- 238000000197 pyrolysis Methods 0.000 title claims abstract description 40
- 239000000463 material Substances 0.000 claims abstract description 43
- 238000000034 method Methods 0.000 claims abstract description 32
- 230000005670 electromagnetic radiation Effects 0.000 claims abstract description 7
- 230000005855 radiation Effects 0.000 claims abstract description 5
- 238000012545 processing Methods 0.000 claims description 36
- 239000000047 product Substances 0.000 claims description 20
- 239000007789 gas Substances 0.000 claims description 19
- 238000006243 chemical reaction Methods 0.000 claims description 14
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 239000012265 solid product Substances 0.000 claims description 11
- 239000002023 wood Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 241000124033 Salix Species 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000013019 agitation Methods 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000003245 coal Substances 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 239000012263 liquid product Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000010902 straw Substances 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 1
- 240000003433 Miscanthus floridulus Species 0.000 description 1
- 241000646858 Salix arbusculoides Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- 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
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J19/12—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
- B01J19/122—Incoherent waves
- B01J19/129—Radiofrequency
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
- C10B19/00—Heating of coke ovens by electrical means
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
- C10B53/00—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
- C10B53/02—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of cellulose-containing material
-
- 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
- C10L5/02—Solid fuels such as briquettes consisting mainly of carbonaceous materials of mineral or non-mineral origin
- C10L5/34—Other details of the shaped fuels, e.g. briquettes
- C10L5/36—Shape
- C10L5/363—Pellets or granulates
-
- 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
-
- 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
- C10L9/00—Treating solid fuels to improve their combustion
- C10L9/08—Treating solid fuels to improve their combustion by heat treatments, e.g. calcining
- C10L9/083—Torrefaction
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G7/00—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals
- F23G7/10—Incinerators or other apparatus for consuming industrial waste, e.g. chemicals of field or garden waste or biomasses
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23K—FEEDING FUEL TO COMBUSTION APPARATUS
- F23K1/00—Preparation of lump or pulverulent fuel in readiness for delivery to combustion apparatus
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2201/00—Pretreatment
- F23G2201/30—Pyrolysing
- F23G2201/302—Treating pyrosolids
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2201/00—Pretreatment
- F23G2201/30—Pyrolysing
- F23G2201/303—Burning pyrogases
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2203/00—Furnace arrangements
- F23G2203/20—Rotary drum furnace
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2204/00—Supplementary heating arrangements
- F23G2204/20—Supplementary heating arrangements using electric energy
- F23G2204/203—Microwave
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23G—CREMATION FURNACES; CONSUMING WASTE PRODUCTS BY COMBUSTION
- F23G2206/00—Waste heat recuperation
- F23G2206/10—Waste heat recuperation reintroducing the heat in the same process, e.g. for predrying
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Environmental & Geological Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- General Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Geology (AREA)
- Thermal Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Sustainable Development (AREA)
- Sustainable Energy (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Electromagnetism (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
A method of treating biomass material, particularly plant-derived biomass material, to produce pyrolysis thereof, comprising subjecting the biomass material to radio frequency electromagnetic radiation, e.g. microwave radiation, while the material is being agitated, under suitable conditions to produce a desired degree of pyrolysis.
Description
Title: Pyrolysis of Biomass Field of the invention s This invention concerns pyrolysis of biomass. The term biomass is used herein to refer to any organic source of energy or chemicals that is renewable, including trees (wood) and other vegetation; agricultural products and wastes (corn, fruit, ensilage, etc.); algae and other marine plants; metabolic wastes (manure, sewage); and cellulosic urban waste. The invention is particularly concerned with plant-derived biomass, such as wood, straw, grass, etc.
Background to the invention is Pyrolysis is the thermal transformation, typically degradation, of material by heating in the absence of oxygen or with limited oxygen (less than the amount required for stoichiometric reaction). Pyrolysis of biomass is a useful technique for the recovery of energy from biomass. Pyrolysis of biomass involves heating biomass, typically to a temperature in the range 400 to 1000 C, and results in a range of possible products including solid products such as char, charcoal, or coke, liquid products such as oils and tar, and low molecular weight gases such as carbon monoxide, carbon dioxide, hydrogen, steam, with the nature and relative amounts of the products depending on reaction conditions.
The present invention concerns an alternative approach to pyrolysis of biomass.
Summary of the invention The present invention provides a method of treating biomass material to produce pyrolysis thereof, comprising subjecting the biomass material to radio frequency electromagnetic radiation while the material is being agitated, under suitable conditions to produce a desired degree of pyrolysis.
Background to the invention is Pyrolysis is the thermal transformation, typically degradation, of material by heating in the absence of oxygen or with limited oxygen (less than the amount required for stoichiometric reaction). Pyrolysis of biomass is a useful technique for the recovery of energy from biomass. Pyrolysis of biomass involves heating biomass, typically to a temperature in the range 400 to 1000 C, and results in a range of possible products including solid products such as char, charcoal, or coke, liquid products such as oils and tar, and low molecular weight gases such as carbon monoxide, carbon dioxide, hydrogen, steam, with the nature and relative amounts of the products depending on reaction conditions.
The present invention concerns an alternative approach to pyrolysis of biomass.
Summary of the invention The present invention provides a method of treating biomass material to produce pyrolysis thereof, comprising subjecting the biomass material to radio frequency electromagnetic radiation while the material is being agitated, under suitable conditions to produce a desired degree of pyrolysis.
The term radio frequency is used herein to refer to frequencies of about 10 kHz and higher. It is preferred to use a radio frequency in the range 300 MHz to 3 THz, more preferably 500 MHz to 300 GHz. It is particularly preferred to use microwave frequency electromagnetic radiation, e.g. having a frequency in the range 500 MHz to 100 GHz, preferably 800 MHz to 5 GHz. It is convenient to use microwave radiation from commercially available microwave generators, which commonly produce microwaves with a frequency of 895 MHz, 915 MHz, 922 MHz or 2450 MHz (2.45 GHz).
io The biomass is preferably plant-derived biomass, particularly wood, straw, grass e.g.
miscanthus, etc. Wood (containing about 15% by weight of water) typically has a calorific value of about 16 MJ/kg.
The biomass material is conveniently in the form of discrete solid pieces. The size and form of the pieces is not critical, but will affect processing to some extent.
The pieces are ideally reasonably uniform in terms of size for uniformity of processing. For ease of handling, the pieces preferably have a maximum dimension of not more than about 100 mm, and are conveniently in the form of chunks, chips, pellets or granules.
Each piece preferably has a volume that does not exceed about 30 cm3 as this has been found experimentally to give the best results. Where the biomass material comprises wood, the wood is conveniently in the form of wood chips, e.g. as obtained from a conventional wood chipping machine. Where the biomass material is in compressed form, e.g.
briquettes, the pieces preferably have a maximum dimension of not more than about 25 mm, more preferably not more than about 10 mm, as heat is retained in the centre of the pieces to a greater extent than with uncompressed, less dense materials, resulting in preferential charring in the centre and hence a less uniform product for larger pieces.
The method is typically carried out in a processing vessel, e.g. a rotating drum as discussed below, having inlet means for supplying material to be treated to the vessel and outlet means for removing the resulting pyrolysed product. The vessel is closed or within a sealed enclosure to prevent unwanted ingress of air, enabling control of the gaseous environment within the vessel and so enabling processing to be carried out in the absence of oxygen or with limited oxygen (less than the amount required for stoichiometric reaction) as is required for pyrolysis to take place.
Processing should be carried out at a processing temperature (in the processing vessel) s that is sufficiently high to ensure that volatile gaseous species (e.g.
steam) released during pyrolysis do not condense in the processing vessel during processing.
Processing is preferably carried out at a processing temperature of at least about 70 C, desirably at least 100 C, or at least 120 C, with the processing temperature preferably not exceeding aboutl75 C.
It is found that pyrolysis in accordance with the invention can be carried out at considerably lower temperatures than those required in conventional pyrolysis techniques, not using radio frequency electromagnetic radiation. This is because the mechanism of radio frequency-induced pyrolysis is such that heating is very limited in the biomass material, which accordingly has a relatively low bulk temperature.
Less energy input is required with the method of the invention compared with conventional methods to produce the same degree of pyrolysis and charring. The method of the invention is thus more energy efficient. A further benefit is that the charred solid end product is at a lower temperature than with conventional techniques, reducing or eliminating the need for cooling, e.g. by water quenching. For example, using willow chips (having a calorific value of about 18 MJ/kg, at a water content of about 15% by wt) as the biomass material, treatment at a processing temperature of 120 C
(compared with about 250 C in conventional thermal pyrolysis methods) produces a torrefied type of willow char (that is brown in colour and has a calorific value of about 22 MJ/kg), with the resulting char product having a temperature of about 70 C on exiting the processing vessel. Similarly a willow charcoal (that is black in colour and has a calorific value of about 26 MJ/kg)) can be produced from the willow chips after rather longer processing at a processing temperature of about 175 C (compared with about 600 C in conventional thermal pyrolysis methods), with the resulting char product having a temperature of about 175 C on exiting the processing vessel.
io The biomass is preferably plant-derived biomass, particularly wood, straw, grass e.g.
miscanthus, etc. Wood (containing about 15% by weight of water) typically has a calorific value of about 16 MJ/kg.
The biomass material is conveniently in the form of discrete solid pieces. The size and form of the pieces is not critical, but will affect processing to some extent.
The pieces are ideally reasonably uniform in terms of size for uniformity of processing. For ease of handling, the pieces preferably have a maximum dimension of not more than about 100 mm, and are conveniently in the form of chunks, chips, pellets or granules.
Each piece preferably has a volume that does not exceed about 30 cm3 as this has been found experimentally to give the best results. Where the biomass material comprises wood, the wood is conveniently in the form of wood chips, e.g. as obtained from a conventional wood chipping machine. Where the biomass material is in compressed form, e.g.
briquettes, the pieces preferably have a maximum dimension of not more than about 25 mm, more preferably not more than about 10 mm, as heat is retained in the centre of the pieces to a greater extent than with uncompressed, less dense materials, resulting in preferential charring in the centre and hence a less uniform product for larger pieces.
The method is typically carried out in a processing vessel, e.g. a rotating drum as discussed below, having inlet means for supplying material to be treated to the vessel and outlet means for removing the resulting pyrolysed product. The vessel is closed or within a sealed enclosure to prevent unwanted ingress of air, enabling control of the gaseous environment within the vessel and so enabling processing to be carried out in the absence of oxygen or with limited oxygen (less than the amount required for stoichiometric reaction) as is required for pyrolysis to take place.
Processing should be carried out at a processing temperature (in the processing vessel) s that is sufficiently high to ensure that volatile gaseous species (e.g.
steam) released during pyrolysis do not condense in the processing vessel during processing.
Processing is preferably carried out at a processing temperature of at least about 70 C, desirably at least 100 C, or at least 120 C, with the processing temperature preferably not exceeding aboutl75 C.
It is found that pyrolysis in accordance with the invention can be carried out at considerably lower temperatures than those required in conventional pyrolysis techniques, not using radio frequency electromagnetic radiation. This is because the mechanism of radio frequency-induced pyrolysis is such that heating is very limited in the biomass material, which accordingly has a relatively low bulk temperature.
Less energy input is required with the method of the invention compared with conventional methods to produce the same degree of pyrolysis and charring. The method of the invention is thus more energy efficient. A further benefit is that the charred solid end product is at a lower temperature than with conventional techniques, reducing or eliminating the need for cooling, e.g. by water quenching. For example, using willow chips (having a calorific value of about 18 MJ/kg, at a water content of about 15% by wt) as the biomass material, treatment at a processing temperature of 120 C
(compared with about 250 C in conventional thermal pyrolysis methods) produces a torrefied type of willow char (that is brown in colour and has a calorific value of about 22 MJ/kg), with the resulting char product having a temperature of about 70 C on exiting the processing vessel. Similarly a willow charcoal (that is black in colour and has a calorific value of about 26 MJ/kg)) can be produced from the willow chips after rather longer processing at a processing temperature of about 175 C (compared with about 600 C in conventional thermal pyrolysis methods), with the resulting char product having a temperature of about 175 C on exiting the processing vessel.
Reaction conditions, particularly reaction time, reaction temperatures and radio frequency, e.g. microwave, power, can be readily selected to produce desired results, having regard to factors including the type of biomass (material, moisture content, size of pieces etc) and desired degree of pyrolysis (and hence degree of charring and relative proportions of char and gas). In general, longer processing produces a solid product with a greater degree of charring and a higher calorific value. It is found that the degree of pyrolysis can be finely controlled by the processing time (typically up to about 45 minutes, and commonly in the range 5 to 30 minutes, typically 15 to 30 minutes, depending on the feedstock properties) and the power density of the radio frequency radiation. The processing temperature is typically in the range 120 C to 175 C, with the resulting product temperature (on exiting the processing vessel) being in the range 70 C
to 175 C.
The biomass material is agitated, i.e. moved and mixed, during treatment, preferably on a continuous basis, to encourage uniformity of processing. This is conveniently achieved by performing the method in a rotating processing vessel e.g. a rotary drum.
Additionally or alternatively, a gas may be passed through the biomass material being treated to cause agitation. The gas may be an inert gas, such as nitrogen. As a further possibility, the gaseous product of the pyrolysis reaction may be drawn off and recirculated through the biomass material, e.g. by being injected from beneath, providing a cheaper source of agitating gas.
The method is conveniently carried out in a rotating vessel such as a drum arranged for rotation about a generally horizontal axis, e.g. as disclosed in WO
2007/007068. The vessel is preferably rotated at a speed in the range 1 to 3 rpm, to cause gentle agitation of the biomass material. The axis of rotation is desirably slightly inclined to promote passage of the material along the vessel, with the angle of inclination being set to produce a desired residence time in the vessel, say about 15 minutes.
The moisture content of the biomass material as supplied for treatment is desirably at least about 10% (w/w), preferably about 15% (w/w) for energy-efficient processing.
Material with a higher moisture content is preferably subjected to a pre-drying step to reduce the water content ideally to about 15% (w/w). It is important that the biomass material has some water content.
The method of the invention produces pyrolysis of the biomass material, resulting in s production of a charred solid product of higher calorific value than the biomass material, and a gaseous product (pyrolysis gas) comprising low molecular weight gases such as carbon monoxide, carbon dioxide, hydrogen, steam, etc. The degree of pyrolysis, and hence charring, depends on treatment conditions, particularly treatment time and the power level of the radio frequency electromagnetic radiation, typically microwave radiation, with longer treatment times and/or higher power levels producing greater degrees of pyrolysis, with more charred products of higher calorific value.
The relative proportions of solid and gaseous products also vary with the degree of pyrolysis, with increased gas being produced with increased pyrolysis levels.
The solid product is useful as a fuel (having an increased calorific value and greater friability compared with the biomass material from which it is derived), with other uses including as activated carbon (as the pyrolysed material has increased porosity), as a sequestering agent (having the benefit of being highly resistant to degradation), and as a soil improvement agent.
The solid product has particular use as a feedstock for coal-fired power stations, to replace or supplement coal. It is particularly preferred to use a char product, e.g. as discussed above, for this purpose. The material has a number of benefits and advantages:
it has a calorific value comparable to that of coal (about 22MJ/kg); it is brittle, and so can be fed directly to the power station without requiring any pre-treatment such as grinding.
The char product thus provides a valuable supplementary plant-derived renewable energy source, which can be easily mixed with coal or utilized singly in existing coal-fired power stations.
The pyrolysis gas may be burnt to harness the energy therein, e.g. in the form of heat, electricity, etc.
The method may be carried out in the substantial absence of oxygen, with no introduced air or oxygen. Alternatively, a small, restricted, controlled amount of air/oxygen may be introduced (less than required for stoichiometric reaction with oxygen) during the pyrolysis reaction. It is found that this results in production of a greater proportion of gas, with a much reduced quantity of char and little tar, in a gassification process.
The method may be carried out batch-wise, but is preferably carried out on a continuous basis.
The invention also covers a charred solid product and/or pyrolysis gas produced by the method of the invention.
The invention also covers use of the charred solid product as a feedstock for a coal-fired power station.
The invention will be further described, by way of illustration, in the following example.
Example Experiments were carried out in a test rig comprising a rotary drum microwave processing vessel generally as described and illustrated in WO 2007/007068.
The test rig comprises a louvered drum generally corresponding to vessel 10 of Figures 1 to 4 of WO
2007/007068, with an associated support cradle 60, feedstock input means 54 and discharge means 56, waveguide 58, enclosure 90 etc, as shown in Figures 5 to 15 of WO
2007/007068. Infrared heaters 84, 86, 88 are mounted inside the enclosure. The drum of the rest rig is of stainless steel and is 1500 mm long and 550 mm in diameter.
The vessel of the test rig was modified in certain respects compared with vessel 10, lacking fins 40 which are not needed when processing biomass and which could be a source of undesirable hot spots, and lacking ceramic tiles 36 as biomass is not generally abrasive.
3o The vessel ideally has weirs at the discharge end, sized to allow a feedstock bed depth of at least twice the penetration depth of the microwaves used. The vessel is mounted with the longitudinal axis at an angle of about 1 to horizontal, with the discharge end below the input end, so that in use the biomass material gradually travels along the vessel. The waveguide 58 is linked to a microwave generator operating at 895 MHz.
In use, a biomass feedstock is introduced to the vessel via the input means, with the vessel being continuously rotated at a speed in the range 1 to 3 rpm to cause gentle agitation. The feedstock travels along the vessel towards the discharge means, being continually gently moved and mixed. Residence time in the vessel is controlled by regulating factors including drum inclination and rotation speed. Microwave energy is introduced to the vessel via the waveguide, causing heating of the feedstock.
This results in pyrolysis of the biomass, producing a charred solid product, low molecular weight gases and possibly also a liquid product such as oils or tar, with the exact products depending on the reaction conditions and the nature of the feedstock. The gaseous product and vapour is extracted from the vessel through the louvre vents in the upper quadrant of the drum, over the full length of the drum, by application of suction. This prevents pressure build up within the vessel, and also prevents possible undesirable secondary reactions. The extracted gas is recycled to the interior of the vessel via suitable pipework, being fed through louvre vents in the bottom quadrant of the drum to permeate up through the biomass bed. The gas assists in agitating the biomass and also helps flush away newly generated gaseous pyrolysis products from the bed from activation sites where they are produced, improving processing efficiency.
Instead of recycling pyrolysis gas in this way, an inert gas such as nitrogen could be injected into the bottom of the biomass bed, but this is more expensive. The processing may be carried out on a continuous basis.
Processing is carried out in the substantial absence of oxygen. To this end, the processing vessel is located in a gas-tight enclosure to prevent ingress of air. The vessel may be initially flushed with an inert gas, e.g. nitrogen, but this is not essential and processing in the presence of air initially present in the vessel gives acceptable results.
In a variant process, processing is carried out with a restricted, controlled amount of oxygen (less than required for stoichiometric reaction) introduced to the vessel during pyrolysis. This results in production of a larger proportion of gas with a much reduced quality of char and little tar in a gassification reaction.
Experiments were carried out using willow chips having a maximum dimension of less than 40 mm as feedstock to the test rig described above. Analysis (in wt %) of the wood chips is as follows:
Moisture 14.4 Volatile matter 71.5 Fixed carbon 13.7 Ash 0.4 -LQQLO-O
Calorific value 18.41 MJ/kg The vessel was preheated by means of infrared heaters mounted inside the drum to raise the temperature of the vessel to about 120 C to prevent condensation of steam.
Feedstock comprising the willow chips was introduced to the drum via the input means, with the vessel rotated at a speed of 1 rpm, with microwave energy at 895 MHz introduced via the waveguide. Gas is recirculated as described above. The feedstock is gently agitated and exposed to microwave energy at a processing temperature of about 120 C, passing slowly along the vessel, with parameters being set to produce a residence time in the drum of approximately 15 minutes. The solid product leaving the drum by the discharge means was in the form of brittle, dark brown pieces of char that is at a temperature of about 70 C on leaving the test rig. Analysis (in wt%) of the char product was as follows:
Moisture 5.4 Volatile matter 61.1 Fixed carbon 31.8 Ash 1.7 0.00 Calorific value 22.49 MJ/kg The char product can be used as a fuel, with particular application as a feedstock for coal-fired power stations, without requiring further treatment, as discussed above.
to 175 C.
The biomass material is agitated, i.e. moved and mixed, during treatment, preferably on a continuous basis, to encourage uniformity of processing. This is conveniently achieved by performing the method in a rotating processing vessel e.g. a rotary drum.
Additionally or alternatively, a gas may be passed through the biomass material being treated to cause agitation. The gas may be an inert gas, such as nitrogen. As a further possibility, the gaseous product of the pyrolysis reaction may be drawn off and recirculated through the biomass material, e.g. by being injected from beneath, providing a cheaper source of agitating gas.
The method is conveniently carried out in a rotating vessel such as a drum arranged for rotation about a generally horizontal axis, e.g. as disclosed in WO
2007/007068. The vessel is preferably rotated at a speed in the range 1 to 3 rpm, to cause gentle agitation of the biomass material. The axis of rotation is desirably slightly inclined to promote passage of the material along the vessel, with the angle of inclination being set to produce a desired residence time in the vessel, say about 15 minutes.
The moisture content of the biomass material as supplied for treatment is desirably at least about 10% (w/w), preferably about 15% (w/w) for energy-efficient processing.
Material with a higher moisture content is preferably subjected to a pre-drying step to reduce the water content ideally to about 15% (w/w). It is important that the biomass material has some water content.
The method of the invention produces pyrolysis of the biomass material, resulting in s production of a charred solid product of higher calorific value than the biomass material, and a gaseous product (pyrolysis gas) comprising low molecular weight gases such as carbon monoxide, carbon dioxide, hydrogen, steam, etc. The degree of pyrolysis, and hence charring, depends on treatment conditions, particularly treatment time and the power level of the radio frequency electromagnetic radiation, typically microwave radiation, with longer treatment times and/or higher power levels producing greater degrees of pyrolysis, with more charred products of higher calorific value.
The relative proportions of solid and gaseous products also vary with the degree of pyrolysis, with increased gas being produced with increased pyrolysis levels.
The solid product is useful as a fuel (having an increased calorific value and greater friability compared with the biomass material from which it is derived), with other uses including as activated carbon (as the pyrolysed material has increased porosity), as a sequestering agent (having the benefit of being highly resistant to degradation), and as a soil improvement agent.
The solid product has particular use as a feedstock for coal-fired power stations, to replace or supplement coal. It is particularly preferred to use a char product, e.g. as discussed above, for this purpose. The material has a number of benefits and advantages:
it has a calorific value comparable to that of coal (about 22MJ/kg); it is brittle, and so can be fed directly to the power station without requiring any pre-treatment such as grinding.
The char product thus provides a valuable supplementary plant-derived renewable energy source, which can be easily mixed with coal or utilized singly in existing coal-fired power stations.
The pyrolysis gas may be burnt to harness the energy therein, e.g. in the form of heat, electricity, etc.
The method may be carried out in the substantial absence of oxygen, with no introduced air or oxygen. Alternatively, a small, restricted, controlled amount of air/oxygen may be introduced (less than required for stoichiometric reaction with oxygen) during the pyrolysis reaction. It is found that this results in production of a greater proportion of gas, with a much reduced quantity of char and little tar, in a gassification process.
The method may be carried out batch-wise, but is preferably carried out on a continuous basis.
The invention also covers a charred solid product and/or pyrolysis gas produced by the method of the invention.
The invention also covers use of the charred solid product as a feedstock for a coal-fired power station.
The invention will be further described, by way of illustration, in the following example.
Example Experiments were carried out in a test rig comprising a rotary drum microwave processing vessel generally as described and illustrated in WO 2007/007068.
The test rig comprises a louvered drum generally corresponding to vessel 10 of Figures 1 to 4 of WO
2007/007068, with an associated support cradle 60, feedstock input means 54 and discharge means 56, waveguide 58, enclosure 90 etc, as shown in Figures 5 to 15 of WO
2007/007068. Infrared heaters 84, 86, 88 are mounted inside the enclosure. The drum of the rest rig is of stainless steel and is 1500 mm long and 550 mm in diameter.
The vessel of the test rig was modified in certain respects compared with vessel 10, lacking fins 40 which are not needed when processing biomass and which could be a source of undesirable hot spots, and lacking ceramic tiles 36 as biomass is not generally abrasive.
3o The vessel ideally has weirs at the discharge end, sized to allow a feedstock bed depth of at least twice the penetration depth of the microwaves used. The vessel is mounted with the longitudinal axis at an angle of about 1 to horizontal, with the discharge end below the input end, so that in use the biomass material gradually travels along the vessel. The waveguide 58 is linked to a microwave generator operating at 895 MHz.
In use, a biomass feedstock is introduced to the vessel via the input means, with the vessel being continuously rotated at a speed in the range 1 to 3 rpm to cause gentle agitation. The feedstock travels along the vessel towards the discharge means, being continually gently moved and mixed. Residence time in the vessel is controlled by regulating factors including drum inclination and rotation speed. Microwave energy is introduced to the vessel via the waveguide, causing heating of the feedstock.
This results in pyrolysis of the biomass, producing a charred solid product, low molecular weight gases and possibly also a liquid product such as oils or tar, with the exact products depending on the reaction conditions and the nature of the feedstock. The gaseous product and vapour is extracted from the vessel through the louvre vents in the upper quadrant of the drum, over the full length of the drum, by application of suction. This prevents pressure build up within the vessel, and also prevents possible undesirable secondary reactions. The extracted gas is recycled to the interior of the vessel via suitable pipework, being fed through louvre vents in the bottom quadrant of the drum to permeate up through the biomass bed. The gas assists in agitating the biomass and also helps flush away newly generated gaseous pyrolysis products from the bed from activation sites where they are produced, improving processing efficiency.
Instead of recycling pyrolysis gas in this way, an inert gas such as nitrogen could be injected into the bottom of the biomass bed, but this is more expensive. The processing may be carried out on a continuous basis.
Processing is carried out in the substantial absence of oxygen. To this end, the processing vessel is located in a gas-tight enclosure to prevent ingress of air. The vessel may be initially flushed with an inert gas, e.g. nitrogen, but this is not essential and processing in the presence of air initially present in the vessel gives acceptable results.
In a variant process, processing is carried out with a restricted, controlled amount of oxygen (less than required for stoichiometric reaction) introduced to the vessel during pyrolysis. This results in production of a larger proportion of gas with a much reduced quality of char and little tar in a gassification reaction.
Experiments were carried out using willow chips having a maximum dimension of less than 40 mm as feedstock to the test rig described above. Analysis (in wt %) of the wood chips is as follows:
Moisture 14.4 Volatile matter 71.5 Fixed carbon 13.7 Ash 0.4 -LQQLO-O
Calorific value 18.41 MJ/kg The vessel was preheated by means of infrared heaters mounted inside the drum to raise the temperature of the vessel to about 120 C to prevent condensation of steam.
Feedstock comprising the willow chips was introduced to the drum via the input means, with the vessel rotated at a speed of 1 rpm, with microwave energy at 895 MHz introduced via the waveguide. Gas is recirculated as described above. The feedstock is gently agitated and exposed to microwave energy at a processing temperature of about 120 C, passing slowly along the vessel, with parameters being set to produce a residence time in the drum of approximately 15 minutes. The solid product leaving the drum by the discharge means was in the form of brittle, dark brown pieces of char that is at a temperature of about 70 C on leaving the test rig. Analysis (in wt%) of the char product was as follows:
Moisture 5.4 Volatile matter 61.1 Fixed carbon 31.8 Ash 1.7 0.00 Calorific value 22.49 MJ/kg The char product can be used as a fuel, with particular application as a feedstock for coal-fired power stations, without requiring further treatment, as discussed above.
Claims (16)
1. A method of treating biomass material to produce pyrolysis thereof, comprising subjecting the biomass material to radio frequency electromagnetic radiation while the material is being agitated, under suitable conditions to produce a desired degree of pyrolysis.
2. A method according to claim 1, wherein the electromagnetic radiation comprises microwave frequency radiation.
3. A method according to claim 1 or 2, wherein the biomass is plant-derived biomass.
4. A method according to any one of the preceding claims, wherein the biomass material comprises pieces having a volume that does not exceed about 30 cm3.
5. A method according to any one of the preceding claims, wherein the biomass material is processed at a processing temperature of at least about 70°C.
6. A method according to claim 5, wherein the biomass material is at a processing temperature of at least about 120°C.
7. A method according to any one of the preceding claims, wherein the biomass material is at a processing temperature not exceeding about 175°C.
8. A method according to any one of the preceding claims, wherein the biomass material is agitated in a rotating vessel.
9. A method according to any one of the preceding claims, wherein the biomass material is agitated by passing gas through the material.
10. A method according to claim 9, wherein the gaseous product of the pyrolysis reaction is recirculated through the biomass material.
11. A method according to any one of the preceding claims, wherein the moisture content of the biomass material is at least about 10% (w/w).
12. A method according to claim 10, wherein the moisture content of the biomass material is about 15% (w/w).
13. A method according to any one of the preceding claims, wherein a restricted amount of air/oxygen is introduced (less than required for stoichiometric reaction with oxygen) during the pyrolysis reaction.
14. A method according to any one of the preceding claims, carried out on a continuous basis.
15. A charred solid product and/or pyrolysis gas produced by the method of any one of the preceding claims.
16. Use of the charred solid product of claim 15 as a feedstock for a coal-fired power station.
Applications Claiming Priority (2)
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GB1003587.1 | 2010-03-04 | ||
GBGB1003587.1A GB201003587D0 (en) | 2010-03-04 | 2010-03-04 | Pyrolysis of biomass |
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CA2700104A1 true CA2700104A1 (en) | 2011-09-04 |
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CA2700104A Abandoned CA2700104A1 (en) | 2010-03-04 | 2010-04-14 | Pyrolysis of biomass |
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US (1) | US20120324785A1 (en) |
EP (1) | EP2542649A2 (en) |
KR (1) | KR20130050281A (en) |
BR (1) | BR112012022133A2 (en) |
CA (1) | CA2700104A1 (en) |
GB (2) | GB201003587D0 (en) |
MX (1) | MX2012010137A (en) |
WO (1) | WO2011107789A2 (en) |
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NZ596549A (en) * | 2011-11-21 | 2014-05-30 | Carbonscape Ltd | Apparatus and method for processing biomass |
US20130276363A1 (en) * | 2012-04-23 | 2013-10-24 | Enginuity Worldwide, Inc. | Moisture Resistant Biomass Fuel Compact and Method of Manufacturing |
WO2013163127A1 (en) * | 2012-04-23 | 2013-10-31 | Enginuity Worldwide, LLC | Moisture resistant biomass fuel compact and method of manufacturing |
NZ702870A (en) * | 2012-06-22 | 2017-12-22 | Suganit Systems Inc | Method and apparatus for treatment of biomass substrates |
US9605211B2 (en) | 2012-09-11 | 2017-03-28 | D4 Energy Group, Inc. | Process and device for devolatizing feedstock |
WO2014152931A1 (en) * | 2013-03-15 | 2014-09-25 | Enginuity Worldwide, LLC | Moisture resistant biomass fuel compact and method of manufacturing |
KR101580621B1 (en) * | 2013-10-24 | 2015-12-28 | 부산대학교 산학협력단 | Bio-coal Using Algae and Method for Manufacturing the Same |
CZ305666B6 (en) * | 2014-08-15 | 2016-01-27 | TESORO Spin off, s.r.o. | Process for preparing biochar-based formulation for plant growth support |
KR20170117454A (en) * | 2015-02-13 | 2017-10-23 | 카본스케이프 리미티드 | Manufacture of graphite from biomass |
CN104891765A (en) * | 2015-05-22 | 2015-09-09 | 成都恩承油气有限公司 | Material drying and thermolysis method |
CN107227160B (en) * | 2017-07-10 | 2018-03-02 | 许可 | A kind of continuous garbage disposal furnace based on magnetic energy carbonization |
KR20230133363A (en) * | 2021-01-21 | 2023-09-19 | 카본 테크놀로지 홀딩스, 엘엘씨 | Biocarbon pellets with adjustable grindability index |
CN112899005A (en) * | 2021-03-23 | 2021-06-04 | 南宁学院 | Carbonization treatment method for biomass material |
CN113061446B (en) * | 2021-04-08 | 2022-05-17 | 广东康帝绿色生物科技有限公司 | Machine-made environment-friendly carbon based on camellia oleifera shells and preparation method thereof |
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US3843457A (en) * | 1971-10-14 | 1974-10-22 | Occidental Petroleum Corp | Microwave pyrolysis of wastes |
JPH04350408A (en) * | 1991-05-29 | 1992-12-04 | Shin Meiwa Ind Co Ltd | Waste material treatment equipment |
US7101464B1 (en) * | 1997-05-09 | 2006-09-05 | The Tire Chief, Inc. | Microwave pyrolysis apparatus for waste tires |
US7301060B2 (en) * | 2003-03-28 | 2007-11-27 | Ab-Cwt, Llc | Process for conversion of organic, waste, or low-value materials into useful products |
US8585788B2 (en) * | 2006-03-31 | 2013-11-19 | Coaltek, Inc. | Methods and systems for processing solid fuel |
US8585786B2 (en) * | 2006-03-31 | 2013-11-19 | Coaltek, Inc. | Methods and systems for briquetting solid fuel |
GB2448531B (en) * | 2007-04-19 | 2012-02-08 | Coal Products Ltd | Fuel briquette |
US10072227B2 (en) * | 2008-07-04 | 2018-09-11 | University Of York | Microwave torrefaction of biomass |
US8466332B1 (en) * | 2011-12-21 | 2013-06-18 | Climax Global Energy | Method and apparatus for microwave depolymerization of hydrocarbon feedstocks |
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2010
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- 2010-04-14 CA CA2700104A patent/CA2700104A1/en not_active Abandoned
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EP2542649A2 (en) | 2013-01-09 |
US20120324785A1 (en) | 2012-12-27 |
KR20130050281A (en) | 2013-05-15 |
BR112012022133A2 (en) | 2016-10-25 |
GB201003587D0 (en) | 2010-04-21 |
GB201215219D0 (en) | 2012-10-10 |
MX2012010137A (en) | 2012-11-30 |
WO2011107789A2 (en) | 2011-09-09 |
GB2490835A (en) | 2012-11-14 |
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