WO2022108687A2 - Microwave-based pyrolysis reactor and associated methods - Google Patents
Microwave-based pyrolysis reactor and associated methods Download PDFInfo
- Publication number
- WO2022108687A2 WO2022108687A2 PCT/US2021/054597 US2021054597W WO2022108687A2 WO 2022108687 A2 WO2022108687 A2 WO 2022108687A2 US 2021054597 W US2021054597 W US 2021054597W WO 2022108687 A2 WO2022108687 A2 WO 2022108687A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- microwave
- waste
- pyrolysis reactor
- cavity
- waste mixture
- Prior art date
Links
- 238000000197 pyrolysis Methods 0.000 title claims abstract description 96
- 238000000034 method Methods 0.000 title claims abstract description 76
- 239000002699 waste material Substances 0.000 claims abstract description 194
- 238000012545 processing Methods 0.000 claims abstract description 32
- 238000012546 transfer Methods 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims description 51
- 239000000523 sample Substances 0.000 claims description 42
- 239000007788 liquid Substances 0.000 claims description 17
- 239000000446 fuel Substances 0.000 claims description 16
- 239000012075 bio-oil Substances 0.000 claims description 12
- 239000004020 conductor Substances 0.000 claims description 10
- 238000009413 insulation Methods 0.000 claims description 9
- 238000003756 stirring Methods 0.000 claims description 8
- 230000008878 coupling Effects 0.000 claims description 6
- 238000010168 coupling process Methods 0.000 claims description 6
- 238000005859 coupling reaction Methods 0.000 claims description 6
- 230000005670 electromagnetic radiation Effects 0.000 claims description 5
- 230000010363 phase shift Effects 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 3
- 230000003321 amplification Effects 0.000 claims description 3
- 238000003199 nucleic acid amplification method Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 description 29
- 230000005684 electric field Effects 0.000 description 28
- 230000008569 process Effects 0.000 description 27
- 238000009826 distribution Methods 0.000 description 22
- 230000008859 change Effects 0.000 description 15
- 239000000463 material Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 238000002156 mixing Methods 0.000 description 11
- 238000004088 simulation Methods 0.000 description 10
- 230000015556 catabolic process Effects 0.000 description 9
- 238000013461 design Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- -1 “cracking”) Chemical compound 0.000 description 8
- 238000013459 approach Methods 0.000 description 7
- 239000006227 byproduct Substances 0.000 description 7
- 239000000356 contaminant Substances 0.000 description 7
- 239000004033 plastic Substances 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 230000035515 penetration Effects 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- 239000002023 wood Substances 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000005672 electromagnetic field Effects 0.000 description 5
- 230000005284 excitation Effects 0.000 description 5
- 239000012467 final product Substances 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 239000010794 food waste Substances 0.000 description 5
- 230000006870 function Effects 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 238000011068 loading method Methods 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 238000003763 carbonization Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000010813 municipal solid waste Substances 0.000 description 4
- 238000007493 shaping process Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 229920006328 Styrofoam Polymers 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000009529 body temperature measurement Methods 0.000 description 3
- 238000004364 calculation method Methods 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 239000000571 coke Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 3
- 238000002309 gasification Methods 0.000 description 3
- 238000007726 management method Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000000813 microbial effect Effects 0.000 description 3
- 230000000737 periodic effect Effects 0.000 description 3
- 238000011027 product recovery Methods 0.000 description 3
- 239000008261 styrofoam Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 239000002028 Biomass Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 230000003044 adaptive effect Effects 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000010828 animal waste Substances 0.000 description 2
- 239000002551 biofuel Substances 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 230000004720 fertilization Effects 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 238000002595 magnetic resonance imaging Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910017464 nitrogen compound Inorganic materials 0.000 description 2
- 150000002830 nitrogen compounds Chemical class 0.000 description 2
- 238000013021 overheating Methods 0.000 description 2
- 239000013618 particulate matter Substances 0.000 description 2
- 229920005547 polycyclic aromatic hydrocarbon Polymers 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical class S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 2
- 229910052815 sulfur oxide Inorganic materials 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- 239000012855 volatile organic compound Substances 0.000 description 2
- 238000012935 Averaging Methods 0.000 description 1
- 230000005457 Black-body radiation Effects 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 244000027321 Lychnis chalcedonica Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000009933 burial Methods 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000004185 countercurrent chromatography Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006324 decarbonylation Effects 0.000 description 1
- 238000006606 decarbonylation reaction Methods 0.000 description 1
- 238000006114 decarboxylation reaction Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000004794 expanded polystyrene Substances 0.000 description 1
- 239000004795 extruded polystyrene foam Substances 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000013611 frozen food Nutrition 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 238000010335 hydrothermal treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000013528 metallic particle Substances 0.000 description 1
- 239000010814 metallic waste Substances 0.000 description 1
- 239000010812 mixed waste Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000002310 reflectometry Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- 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
-
- 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
- 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
- C10B53/07—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of solid raw materials consisting of synthetic polymeric materials, e.g. tyres
-
- 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
- C10B7/00—Coke ovens with mechanical conveying means for the raw material inside the oven
- C10B7/10—Coke ovens with mechanical conveying means for the raw material inside the oven with conveyor-screws
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
- C10G1/002—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal in combination with oil conversion- or refining processes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G9/24—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by heating with electrical means
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1003—Waste materials
Definitions
- Pyrolysis is the process of heating waste in an inert environment to induce thermal decomposition of the waste. This thermal decomposition changes the chemical composition of the waste, resulting in by-products with a host of industrial and commercial uses. When the waste contains organic matter, any resulting solid residue is typically high in carbon, taking the form of char. However, pyrolysis may also generate gaseous and liquid by-products, depending on the composition of the waste. Applications of pyrolysis include the conversion of biowaste to syngas and biochar, the production of coke from coal, the production of charcoal from wood, the conversion of ethane to ethylene (i.e., “cracking”), and waste management.
- microwave heating offers improved thermal efficiency and reaction speed.
- Microwave heating uses Joule losses of the electric field, combined with electrical conductivity of the waste material at GHz frequencies, to increase waste temperature. Because of the high penetration depth of electromagnetic waves in the radio-frequency spectrum, this type of heating may be confined within a volume possibly without damage or overheating of the surface, which is difficult to achieve with convection heating. This localized heating also improves system efficiency by directly producing heat inside the intended material, and therefore the heating rate is not limited due to thermal conductivity to an external heat source and the heat capacity of the material.
- the present embodiments feature pyrolysis reactors that use microwaves to rapidly heat waste materials.
- microwave cavities within which the waste materials are located. Electromagnetic modes of the cavities are excited by electromagnetic fields that are coupled into the cavity by one or more microwave probes (or launchers) driven by an external microwave source.
- the present embodiments advantageously use a number of techniques to ensure appropriate distribution of the electromagnetic energy throughout the cavity, thereby ensuring that the waste materials are rapidly and more uniformly heated (as compared to operation without these techniques). As described in more detail below, these techniques include overmoding of the cavity, outphasing, amplitude modulation, and frequency modulation. Unlike many prior-art pyrolysis reactors, the present embodiments are not adversely affected by the moisture content of the waste, and may even perform better when water is intentionally added to the waste.
- the pyrolysis reactors of the present embodiments feature spatial power combining, within the cavity, of electromagnetic power from several solid-state sources.
- magnetron sources e.g., as typically used in conventional microwave ovens
- Solidstate sources do not achieve as high power as magnetrons, but with spatial power combining, high microwave power levels (e.g., up to tens of kilowatts) can be achieved inside the cavity using solid-state amplifiers.
- high microwave power levels e.g., up to tens of kilowatts
- the amplifiers can be operated nonlinearly.
- the microwave cavity can be excited using multiple probes that are all driven by solid-state power amplifiers, which are excited by one or more microwave oscillators. Dynamic relative phase shifting of the power amplifier outputs can be used to improve heating efficiency of the waste in the cavity.
- a radio frequency (RF) applicator delivers electromagnetic energy to a treatment volume containing an emulsion of a hydrocarbon and a substrate, which facilitates separation of the hydrocarbon and substrate molecules into layers. Hydrocarbons and other products can then be recovered from their respective layers (e.g., see US Patent No. 7,486,248). Microwave heating has also been shown to be much faster than conventional resistance heating in hydrothermal treatments.
- the present embodiments can be used to process both large and small quantities of waste mass, and are therefore scalable while maintaining high energy conversion efficiency.
- This scaling can be implemented via (1) selection of the cavity size and frequency, (2) microwave power density by power combining the outputs of multiple solid-state amplifiers, (3) overall power using solid-state amplifiers, (4) time-domain profile when the power is on, and (5) mode-mixing through one or more of mechanical means, frequency modulation, and varying the cavity boundary conditions.
- FIG. 1 shows a micro wave-based pyrolysis reactor, in an embodiment.
- FIG. 2 shows a micro wave-based pyrolysis reactor, in an embodiment.
- FIG. 3 illustrates a microwave-based pyrolysis reactor that modulates electromagnetic power coupled to each of its probes, in an embodiment.
- FIG. 4 illustrates a coaxial auger in a microwave cavity of one microwave-based pyrolysis reactor for stirring waste, according to an embodiment.
- FIGS. 5 and 6 collectively illustrate a microwave-based pyrolysis reactor and a frequency- selective surface, in an embodiment.
- FIG. 7 is a flowchart illustrating a method for processing waste with a pyrolysis reactor, in an embodiment.
- FIG. 8 illustrates a system that processes waste with a pyrolysis reactor to produce liquid fuel, in an embodiment.
- FIG. 9A shows a simulated microwave cavity with dimensions used for calculation.
- FIG. 9B shows calculated magnitude of electric field inside the cavity of FIG. 9A containing low permittivity mixed-density polyethylene.
- FIG. 9C shows calculated magnitude of electric field inside the cavity of FIG. 9A containing high permittivity food mixture.
- FIG. 10 shows simulated electric field distribution within a cylindrical microwave cavity that includes 17 probes.
- FIG. 11 shows a simulation setup for thermal distribution calculation.
- FIG. 12 shows the effect of a small frequency shift (6 MHz) in the field distribution in an empty microwave cavity in a simulation.
- FIG. 1 is a perspective view of a microwave-based pyrolysis reactor 100 that uses electromagnetic energy to induce thermal breakdown of a waste mass 102.
- Waste mass 102 may include one or more of several types of waste, such as biowaste (e.g., food scraps, vegetation, animal waste), wood-based products (e.g., paper, wood), metals (e.g., aluminum), Styrofoam, plastic, crude oils, microalgae, and lignocellulosic biomasses.
- waste mass 102 may contain liquids, such as water, that rapidly absorb electromagnetic energy in the microwave region of the electromagnetic spectrum, and increase the speed with which waste mass 102 is heated.
- An output chute 104 may be used to collect solid and liquid byproducts as they form and drop to the bottom of pyrolysis reactor 100.
- Gaseous byproducts may be collected with a pump 142 that evacuates an inner volume 112 of pyrolysis reactor 100 via a pump port 106.
- gaseous byproducts include particulate matter, volatile organic compounds, polynuclear aromatic hydrocarbons, methane, ammonia, carbon monoxide, hydrogen sulfide, hydrogen cyanide, and sulfur oxides. While waste mass 102 is shown in FIG. 1 as a rectangular prism, it may alternatively have a different shape, provided that it fits within inner volume 112.
- Pyrolysis reactor 100 includes a microwave cavity 110 formed by electrically conductive walls 114 that surround inner volume 112. Electrically conductive walls 114 may be made of metal (e.g., copper, silver, gold, aluminum, etc.). Microwave cavity 110 supports a plurality of electromagnetic modes that store electromagnetic energy when excited.
- microwave cavity 110 is a cylinder in which the conductive walls 114 form a cylindrical shell having a length in the z direction (see right-handed coordinate system 150) and a radius in the transverse x-y plane.
- microwave cavity 110 may have a different geometry without departing from scope hereof.
- microwave cavity 110 may be shaped as a rectangular cuboid, a square cuboid, or another type of hollow three-dimensional prism.
- Microwaves are coupled into the microwave cavity 110 through one or more probes 122, each driven by a corresponding amplifier 120.
- first and second probes 122(1), 122(2) couple electromagnetic energy into the microwave cavity 110, where waste mass 102 absorbs the electromagnetic energy, converting it to heat that increases the temperature of waste mass 102 and results in breakdown of waste mass 102.
- power to each amplifier 120 may be optimized to increase the amount of electromagnetic power delivered to waste mass 102, in turn increasing the speed at which waste mass 102 increases in temperature and therefore breaks down. More than two probes 122 (e.g., four, ten, twenty-eight, fifty or other number) may be used without departing from the scope hereof.
- FIG. 1 shows first and second probes 122(1), 122(2) located on opposite sides of microwave cavity 110 (in the x direction) and at the same z position, probes 122 may be located at different positions without departing from the scope hereof.
- Probes 122 are driven with an electrical microwave signal 131 that is generated by a frequency source 130 and split with a power splitter 132.
- Microwave signal 131 may have a single frequency selected to resonate with one of the modes of microwave cavity 110.
- the frequency may be selected to coincide with the lowest-frequency fundamental resonance of microwave cavity 110 (when the cavity is empty, i.e., not loaded).
- microwave cavity 110 may be overmoded, i.e., driven at a frequency higher than that of the fundamental resonance to excite several modes.
- microwave signal 131 contains a plurality of frequencies.
- each amplifier 120(1), 120(2) may be a high-efficiency solid-state amplifier based on GaN or LDMOS power transistors. Each amplifier 120(1), 120(2) may output several watts of power, or more, depending on the volume and contents of waste mass 102.
- the frequency of microwave signal 131 may be selected near 2.45 GHz or 900 MHz, where the electromagnetic energy has sufficient penetration depth given the electrical conductivity of most waste materials. Therefore, the use of these frequencies may help ensure uniform heating and even thermal breakdown throughout all of waste mass 102.
- the frequency of microwave signal 131 lies within the Industrial, Scientific, and Medical (ISM) band between 2.4 and 2.5 GHz.
- each amplifier 120(1), 120(2) may be based on GaN power transistors.
- the frequency of microwave signal 131 lies within the ISM band between 915 and 928 MHz.
- each amplifier 120(1), 120(2) may be based on either GaN power transistors or LDMOS power transistors
- the frequency of microwave signal 131 is not limited to only these bands, provided that the cavity is shielded.
- pyrolysis reactor 100 may operate with powers up to tens of kilowatts, or more, operation at frequencies within ISM bands advantageously minimizes the likelihood of generating interference that can disrupt telecommunications.
- pyrolysis reactor 100 operates at multiple frequencies simultaneously. For example, first probe 122(1) may be driven near the ISM band at 915 MHz, while second probe 122(2) is driven near the ISM band at 2.45 GHz. The use of multiple frequencies can help ensure uniform heating given the different absorption properties of materials within waste mass 102, and how these absorption properties change as the waste mass 102 breaks down.
- Additional ISM bands are centered at 5.8 GHz, 24.125 GHz, 61.25 GHz, 433.92 MHz, 40.68 MHz, etc. Additional probes 122 may be driven at frequencies within these additional ISM bands to further increase the frequency diversity of the electric field within microwave cavity 110. Since the number of transverse-electric (TE) and transverse-magnetic (TM) modes within the microwave cavity 110 scales as f 3 , where f is the frequency of the microwave signal 131, operating microwave cavity 110 at higher frequencies can advantageously facilitate overmoding. However, a higher frequency usually results in a lower efficiency of solid-state amplifiers 120, and less penetration of the waste due to a smaller skin depth. Thus, there is a trade-off between overmoding and efficiency that can be evaluated based on the design requirements.
- TE transverse-electric
- TM transverse-magnetic
- FIG. 2 is a perspective view of a microwave-based pyrolysis reactor 200 that uses time-varying outphasing to increase the efficiency with which power is coupled out of amplifiers 120(1), 120(2) and into waste mass 102.
- Pyrolysis reactor 200 is similar to pyrolysis reactor 100 of FIG. 1 except that it includes a signal processing module 210 that controls a variable phase shifter 214 with a phase-control signal 208 to change the relative phase A between first and second drive signals 206(1), 206(2) that are fed to first and second amplifiers 120(1), 120(2), respectively.
- the relative phase A is selected to maximize constructive interference between the electromagnetic fields near waste mass 102, which in turn maximizes the power density and thus absorption by waste mass 102. Additionally, outphasing can improve amplifier efficiency when the load is varying.
- signal processing module 210 monitors waste mass 102 to determine how microwave properties (e.g., real and imaginary components of the permittivity) change as waste mass 102 heats and breaks down.
- waste mass 102 may be thought of as a microwave load that varies spatially and temporally.
- signal processing module 210 may use a plurality of thermocouples 212 to record temperatures of waste mass 102 at various positions, both at the surface of waste mass 102 and inside waste mass 102.
- Signal processing module 210 may additionally or alternatively use one or more infrared cameras (e.g., infrared camera 207 as shown) to record a temperature distribution of waste mass 102.
- Infrared camera 207 may view waste mass 102 via a viewport 204.
- Signal processing module 210 processes this temperature data to determine the optimum phase shift A , and then outputs corresponding phase-control signal 208.
- Signal processing module 210 may operate as part of a feedback loop.
- pyrolysis reactor 200 uses radiometry at microwave frequencies to measure the properties of waste mass 102 at depths of several centimeters. This embodiment advantageously overcomes limitations of infrared camera 207, which can only detect the temperature of waste mass 102 to within a few millimeters of its surface. Radiometry may also provide a greater density of spatial temperature measurements than can be implemented with the plurality of thermocouples 212.
- pyrolysis reactor 200 additionally includes a radiometer 209 for receiving the emitted black-body radiation in the microwave region of the spectrum where the skin depth in waste is comparable to the waste dimensions.
- FIG. 2 shows pyrolysis reactor 200 with two probes 122(1), 122(2)
- pyrolysis reactor 200 may include a plurality of n probes 122, where n is an integer greater than or equal to 2.
- the output of frequency source 130 is split into n drive signals 206 that are amplified by n corresponding amplifiers 120 to drive the n probes 122.
- Signal processing module 210 processes the temperature data to determine n — 1 optimum phase shifts A -L, ... , ⁇ pn- for maximizing power absorbed by waste mass 102.
- Signal processing module 210 then outputs n — 1 corresponding phase-control signals 208 that control corresponding n — 1 variable phase shifters 214. Since only relative shifts need to be controlled for outphasing, one of the n drive signals 206 does not need to be phase shifted.
- FIG. 3 illustrates how micro wave-based pyrolysis reactor 200 of FIG. 2 can be additionally configured to modulate the electromagnetic power coupled to each of probes 122.
- thermocouples 212, infrared camera 207, and variable phase shifter 214 are not shown in FIG. 3.
- Signal processing module 210 processes received temperature data to determine n amplitudes, or power levels, at which each the n probes 122 should be driven to control the power absorbed by waste mass 102 in addition to outphasing.
- variation of the power levels throughout the pyrolysis process can be used to maintain high efficiency as the electrical properties of waste mass 102 changes as it breaks down. Such a variation in power levels is difficult to implement in a conventional magnetron-based microwave reactor.
- each amplifier 120(1), 120(2) includes a power amplifier 320(1), 320(2) driven by a corresponding driver amplifier 322(1), 322(2).
- the main purpose of each driver amplifier 322 is gain, not efficiency. However, if the gain of the corresponding power amplifier 320 is low, then the efficiency of driver amplifier 322 affects overall efficiency.
- Each power amplifier 320 and driver amplifier 322 is powered by a DC power supply 326 via a corresponding modulator 324.
- Each modulator 324 is controlled via a corresponding modulation signal 326 to change the power outputted by corresponding amplifier 320, 322. In some embodiments, only power amplifiers 320(1), 320(2) are modulated.
- both driver amplifiers 322(1), 322(2) and power amplifiers 320(1), 320(2) are modulated.
- FIG. 2 shows one example of frequency modulation, wherein frequency source 130 is a voltage-controlled oscillator driven with a frequency-control signal 218 that changes the frequency of microwave signal 131.
- Frequency-control signal 218 may be generated by signal -processing module 210, as shown in FIG. 2, in response to certain detected temperatures, temperature gradients, or temperature distributions. Alternatively, frequency-control signal 218 may be generated by a circuit separate from signal-processing module 210.
- Frequency-control signal 218 may be a periodic signal (e.g., sine wave, triangle wave, sawtooth) such that the frequency modulation is periodic.
- waste mass 102 responds to a time-averaged electric field at each spatial point within microwave cavity 110, where the time averaging is over one period of frequency— control signal 218.
- frequency— control signal 218 may be random (e.g., white noise) or include a random component (e.g., a triangle wave superimposed with white noise).
- FIG. 4 is a side view of a microwave-based pyrolysis reactor 400 that is similar to pyrolysis reactors 100, 200 of FIGS. 1 and 2, except that it uses a coaxial microwave cavity 410 instead of a hollow microwave cavity.
- a mixing auger 422 serves as a linear electrical conductor (hereinafter a “center” conductor) of the coaxial microwave cavity 410, and may be made of metal with high electrical conductivity (e.g., copper, silver, aluminum, etc.).
- Mixing auger 422 includes one or more helical paddles 426 attached to a spindle 424 that is rotated by a motor 412. As mixing auger 422 rotates, paddles 426 mix waste mass 102 to help insure thermal uniformity of waste mass 110. For clarity of illustration, waste mass 102 is not shown in FIG. 4.
- spindle 424 is made of metal and paddles 426 are made of a non-electrically conductive material, such as ceramic, that can withstand the high temperatures achieved within pyrolysis reactor 400. Therefore, in these embodiments, only spindle 424, and not paddles 426, serves as the center conductor of coaxial microwave cavity 410. In other embodiments, paddles 426 are also made of metal and are in electrical contact with spindle 424. In these embodiments, both spindle 424 and paddles 426 serve as the center conductor of coaxial microwave cavity 410. While FIG. 4 shows pyrolysis reactor 400 with two probes 122, pyrolysis reactor 400 may have more than two probes 122 (e.g., 4, 10, 28, 50, etc.) without departing from the scope hereof.
- FIGS. 5 and 6 show a micro wave-based pyrolysis reactor 500 that is similar to pyrolysis reactor 100 of FIG. 1 except that it includes a frequency-selective surface 502.
- Frequency-selective surface 502 is mounted in front of electrically conductive wall 514, which may be electrically grounded, to form microwave cavity 510 (similar to microwave cavity 110 in earlier figures).
- frequency-selective surface 502 may be configured to appear as an inductive, capacitive, or resonant surface.
- the tangential electric field of the cavity’s modes do not need to equal zero at frequency-selective surface 502 (unlike electrically conductive wall 514, where the tangential electric field always equal zero).
- frequency- selective surface 502 provides a mechanism to further alter the energy distribution within inner volume 512 of cavity 510.
- frequency-selective surface 502 may be used to create an energy distribution that is spatially more uniform, as compared to the energy distribution of the modes that are obtained when cavity 510 excludes frequency-selective surface 502.
- Frequency-selective surface 502 is shown in FIG. 5 as a two-dimensional square grid of elements 504 formed on a dielectric substrate 506.
- each element 504 is a Jerusalem cross formed from metal (e.g., copper).
- a dielectric overlayer may be placed on top of elements 504. Dielectric substrate 506 (and the dielectric overlayer, when included) may be flexible so that frequency- selective surface 502 can conform to the curvature of electrically conductive wall 514.
- Frequency-selective surface 502 may be configured differently than shown in FIGS. 5 and 6.
- each element 504 may be a different type of N-pole element (e.g., straight dipole, tripole, square spiral, etc.), loop-type element (e.g., three-legged loaded element, four-legged loaded element, hexagon element), plate-type element with solid interior (e.g., square, hexagon, circle, etc.), or a combination thereof.
- elements 504 may be arranged in a different type of grid (e.g., hexagonal, triangular, rectangular, interlaced, closely-packed, etc.).
- Other design parameters e.g., element size, spacings between neighboring elements, thickness of dielectric substrate 506, etc. may be selected to achieve a particular boundary condition that gives a desired electric field distribution.
- frequency- selective surface 502 subtends an azimuthal angle ⁇ p with respect to a cylindrical axis 602 of microwave cavity 510, and is located a radial distance 504 in front of electrically conductive wall 514 (i.e., toward cylindrical axis 602).
- frequency- selective surface 502 may subtend a different azimuthal angle than shown.
- frequency- selective surface 502 may have a height, in the z direction, of any value less than or equal to the height of electrically conductive wall 514.
- frequency-selective surface 502 azimuthally subtends 360° and has a height equal to that of wall 514, thereby fully covering wall 514.
- an additional frequency-selective surface is placed over one or both of the flat circular top and bottom walls 514 of cylindrical microwave cavity 510. Similar frequency-selective surfaces may be placed in front of electrically conductive walls of a microwave cavity having a different shape. For example, when microwave cavity 510 is rectangular, one or more planar frequency-selective surfaces may be placed in front of these flat walls of the rectangular cavity 510.
- multiple frequency-selective panels 502 are placed in front of walls 514 of microwave cavity 510.
- frequency- selective panels 502 with different electrical properties are used in different regions of microwave cavity 510 to account for spatial variations of waste mass 102.
- a first frequency-selective panel 502 may be used at the top of microwave cavity 510 (in the +z direction) to create a first electric field distribution that is matched to that portion of waste mass 102 at the top of the inner volume 512.
- a second frequency-selective panel 502 may be used at the middle of microwave cavity 510 to create a second electric field distribution that is matched to that portion of waste mass 102 at the middle of the inner volume 512.
- a third frequency-selective panel 502 may be used at the bottom of microwave cavity 510 to create a third electric field distribution that is matched to that portion of waste mass 102 at the bottom of inner volume 512.
- the third frequency- selective panel 502 may be designed to optimally heat the char and ash, while the first and/or second frequency-selective panels 502 may be designed to optimally heat that portion of waste mass 102 that has not yet been converted to char and ash.
- water may be added to waste mass 102 within the inner volume 112, 512 to facilitate thermal conduction of heat within waste mass 102.
- the water may be salt water.
- small metallic particles e.g., nanoparticles
- small metallic particles may be added to waste mass 102 (either with or without additional water added) to enhance scattering of the electromagnetic fields throughout waste mass 102, thereby improving the uniformity with which the electromagnetic energy is absorbed by waste mass 102.
- the microwave cavity 110, 510 may be externally surrounded with thermal shielding, for example in space 553, to reduce heat loss, thereby improving the energy efficiency of the pyrolysis reactor.
- this thermal shielding may be made of a material having low thermal conductivity (e.g., fiberglass, ceramic, Styrofoam, plastic, etc.) to minimize convective heat loss from the microwave cavity to the surrounding environment.
- a heat shield e.g., aluminum foil, steel panels, ceramic thermal barriers
- the microwave cavity is placed within a larger vacuum system that may be evacuated to reduce convective heat loss from the microwave cavity.
- wall 551 confines vacuum space 553, in which microwave cavity 510 is placed.
- Wall 551 of the larger vacuum system may be made of metal to act as heat shield.
- the features described above with respect to the pyrolysis reactors 100, 200, 400, and 500 may be combined in any way without departing from the scope hereof.
- the present embodiments include all combinations of: the outphasing shown in FIG. 2, the frequency modulation shown in FIG. 2, the amplifier modulation shown in FIG. 3, the use of frequency- selective surfaces shown in FIG. 5, and overmoding. Any of these combinations may be further implemented with the mixing auger 422 to form the coaxial microwave cavity 410 of FIG. 4.
- FIG. 7 is a flowchart illustrating a method 700 for processing a waste mixture using a pyrolysis reactor.
- Method 700 may be implemented by part or all of any of pyrolysis reactors 100, 200, 400, and 500.
- Method 700 includes steps 740 and 760. However, in other embodiments method 700 may further include one or more of steps 710, 720, 730, and 750.
- Method 700 may be implemented with a pyrolysis reactor storing a waste mass (used interchangeably with “waste mixture” herein) within an internal space of a microwave cavity.
- method 700 includes placing the waste mass (e.g., waste mass 102 of FIG. 1) into the microwave cavity (e.g., microwave cavity 110).
- the waste mass may include one or more types of waste, such as biowaste (e.g., food scraps, vegetation, animal waste), wood-based products (e.g., paper, wood), metals (e.g., aluminum), Styrofoam, plastic, crude oils, microalgae, and lignocellulosic biomasses.
- the heating profile as described in steps below, may be configured specifically for the types of waste present in the waste mass.
- waste mass containing liquid such as water, absorbs electromagnetic energy in the microwave region of the electromagnetic spectrum more rapidly and, therefore heats up faster, than waste mass with less liquid, and may require a different heating profile.
- additives may be added to the waste mass, such as one or more of water, salt water, and metal or dielectric nanoparticles.
- a microwave signal is generated with an oscillator.
- probes 122 of FIG. 1 are driven with microwave signal 131 that is generated by frequency source 130.
- the generated microwave signal is split into a plurality of drive signals.
- one oscillator may generate drive signals for all probes in the microwave cavity.
- microwave signal 131 from oscillator 130 is split with power splitter 132 into the n drive signals 206, where n is an integer greater than 1.
- Microwave signal 131 may have a single frequency selected to resonate with one of the modes of microwave cavity 110.
- microwave cavity 110 may be overmoded, i.e., driven at a frequency higher than that of the fundamental resonance to excite multiple modes.
- Step 730 includes amplifying the plurality of drive signals into a corresponding one of a plurality of amplified signals. This amplification is for example achieved using a solid-state power amplifier for each probe.
- the amplified drive signals are coupled into the microwave cavity to excite a plurality of cavity modes.
- one or more probes 122, each driven by a corresponding amplifier 120 excites microwave modes in microwave cavity 110 (see FIG. 2).
- probes 122(1) and 122(2) couple electromagnetic energy into microwave cavity 110, where waste mass 102 absorbs the electromagnetic energy, converting it to thermal energy that increases the temperature of waste mass 102 and results in breakdown of waste mass 102.
- Multiple probes and amplifiers 122 increase the electromagnetic power delivered to waste mass 102, in turn increasing the speed at which waste mass 102 increases in temperature and therefore breaks down.
- Step 750 includes measuring one or more temperatures of the waste mass.
- Step 750 is, for example, performed with thermocouples 212 in FIG. 2.
- the temperature measurements are used to determine the relative phases for the variable phase shifters, thereby phase-shifting one or more of the plurality of drive signals.
- signal processing module 210 monitors waste mass 102 to determine how its microwave properties (e.g., real and imaginary components of the permittivity) change as it heats and breaks down.
- waste mass 102 may be thought of as a microwave load that varies spatially and temporally.
- signal processing module 210 may use thermocouples 212 to record temperatures of waste mass 102 at various positions, both at the surface and inside waste mass 102.
- Step 750 may also include recording a thermal image stream of the waste mixture using an infrared camera.
- infrared camera 207 records a temperature distribution of waste mass 102 through viewport 204.
- Infrared camera penetrates only a few millimeters into the water volume due to the limited skin depth. For this reason, the image stream from the infrared camera may be used in conjunction with thermocouples 212 placed at various locations and depth of waste mass 102.
- step 750 includes, instead of or in addition to the infrared camera, a microwave radiometer (e.g., radiometer 209 in FIG. 2) that measures thermally-emitted electromagnetic radiation from waste mass 102.
- a microwave radiometer e.g., radiometer 209 in FIG. 2
- at least one phase-control signal is determined based on the measured temperatures.
- processing module 210 monitors the measured temperatures at various locations including at the surface and inside of waste mass 102, to determine how its microwave properties (e.g., real and imaginary components of the permittivity) change as waste mass 102 heats and breaks down. As waste mass 102 undergoes changes, the thermal load changes as a function of space and time.
- the relative phase is continuously updated to maintain thermal efficiency and uniformity.
- This process requires accurate measurements of temperature at as many locations in the cavity as possible.
- an infrared camera e.g., infrared camera 207
- a microwave radiometer e.g., radiometer 209
- step 760 the one or more phase-control signals are outputted to a one or more corresponding variable phase-shifters.
- signal processing module 210 outputs the relative phase 208 to variable phase shifter 214 for probe 122(2).
- the number of variable phase shifters, and therefore the number of phase-control signals may be one less than the number of probes.
- a different number of phase shifters and corresponding phase control signals may be used without departing from the scope hereof.
- step 760 the phase-adjusted drive signal from each phase-shifter is fed into a corresponding power amplifier of step 730. Accordingly, steps 730, 740, 750 and 760 may be iterated until the waste is fully converted into one or more intermediary compounds that can be used for up-conversion, fuel, or environmentally safe products that can be used for, for example, fertilization.
- Method 700 may include additional steps without departing from the scope hereof.
- method 700 may include, for example, stirring the waste mixture with an auger located at least partially within the internal space of the microwave cavity.
- mixing auger 422 may be rotated by motor 412 to mix waste mass 110, thereby improving thermal uniformity of waste mass 110.
- Method 700 may also include additional or alternate steps to maintain an optimal level of power transfer, or heating efficiency, for efficient breakdown of waste.
- One such step includes improving electric field uniformity inside the microwave cavity by implementing mode mixing using frequency modulation.
- frequency source 130 is a voltage-controlled oscillator driven with frequency— control signal 218 that changes the frequency of microwave signal 131.
- the frequency-modulation control signal 218 may be generated by signal-processing module 210 in response to certain detected temperatures, temperature gradients, or temperature distributions.
- the frequency-modulation control signal may also be random (e.g., white noise) or include a random component (e.g., a triangle wave superimposed with white noise) to further enhance spatial uniformity.
- the steps in method 700 may be modified to accommodate design choices in hardware.
- the cavity design may include frequency selective surfaces, as shown in FIGS. 5 and 6, to modify boundary conditions near the inner walls of the cavity.
- time-domain pulse shaping may be used with a DC power source to enable superposition of modes.
- any microwave pyrolysis reactor including magnetron-based microwave reactor, has advantages over a conventional convection-based reactor, with those advantages being (1) improved thermal efficiency, leading to more rapid thermochemical process to take place and (2) improved thermal uniformity (e.g., not overheating certain parts, such as the surface of waste mass) due to high penetration depth of electromagnetic waves in the radio-frequency spectrum.
- solid-state-based microwave pyrolysis reactor disclosed herein has additional advantages over a conventional magnetron-based microwave reactor with the most important advantage being that the solid-state-based microwave pyrolysis reactor can be scaled in terms of (1) waste mass by cavity size and frequency choice, (2) microwave power density by power combining a plurality of solid-state amplifiers, and (3) overall power by mode-mixing through mechanical, frequency and/or cavity boundary condition design. Additionally, in such a system, byproducts of the pyrolysis process can be further processed to produce liquid fuel, which in turn may at least partially power pyrolysis reactor.
- waste processing system 800 a waste mass 802 is placed in the microwave cavity of pyrolysis reactor 810 and is processed following method 700.
- Dirty biooil 870 from the pyrolysis process has characteristics that vary according to the initial composition of waste mass 802. However, there are some contaminants that negatively influence the quality of the final product of the system.
- liquid fuel 890 as the final product in system 800, may contain contaminants including nitrogen, sulfur, and metal-containing compounds.
- waste processing system 800 includes a co-product recovery module 874 that analyzes dirty bio-oil 870 for these contaminants, and removes any such contaminants that are found.
- co-product recovery module 874 Some of the analysis techniques that may be used in co-product recovery module 874 include gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS) for compound identification and quantitation. Removal of the contaminants from dirty bio-oil 870 may involve one of more compound separation techniques, such as counter current chromatography.
- GC-MS gas chromatography-mass spectrometry
- LC-MS liquid chromatography-mass spectrometry
- the waste processing system 800 includes a microbial upgrading module 872 that uses a sequence of one or more microbial bioreactors to remove these harmful compounds, especially sulfur and nitrogen.
- An example bioreactor may have an established mixed culture dominated by strains of Pseudomonas, Klebsella, or other genera that metabolize contaminating nitrogen compounds.
- the sequence of bioreactors is optimized, such that the broadest and the highest toxic compounds in dirty bio-oil 870 are removed first. This type of optimization may prolong and enhance the stability of the biological treatment processes.
- system 800 After the removal of harmful contaminants, the product of system 800 is clean biofuel.
- dirty bio-oil 870 after having toxic and harmful contaminants removed by co-product recovery module 874 and microbial upgrading module 872, becomes the final product of system 800, i.e., liquid fuel 890.
- Liquid fuel 890 may be sold as clean biofuel 886.
- system 800 may recycle all or a portion of the final product to at least partially power the pyrolysis reactor. More specifically, in some embodiments, system 800 includes an electric generator 892. Electric generator 892 may use all or portion of liquid fuel 890 to generate electricity 884 that can be combined with external power source 882 and supply electricity to pyrolysis reactor 810. Accordingly, pyrolysis reactor 810 can be powered fully or partially by an external power source 882, by electric generator 892 using liquid fuel 890 or by a combination of both sources.
- dT /dt a reasonable approximation for the temperature change dT /dt is given by dT 0.239 x 10“ 6 ⁇ P dt C - where P is the power in watts, C the specific heat in cal/g, and p is the volume mass density in g/cm 3 .
- the efficiency of incineration methods is informally quantified by the amount of diesel energy required to produce carbon-rich products from waste.
- the input is electrical power and the total efficiency will depend on (1) the primary electrical power source efficiency, (2) the microwave generation chain efficiency, and (3) the efficiency of power delivery to the waste mass over time.
- a rate efficiency can be defined as: where V is the volume of the mixed waste (making it difficult to define mass), P is the power in watts required to heat the waste, and T is the time required to reach an average temperature T. We control power and time separately, but one can also quantify it in terms of energy (e.g., joules). This definition of rate efficiency scales in volume.
- the input power in the rate efficiency 77 is the electrical power delivered to the microwave source.
- the heat energy dissipated in the waste mass can be expressed as: where a(x, y, z, t, T is the non-uniform waste conductivity, which is a function of temperature and therefore time.
- the total electric field magnitude is also a function of position within the waste volume and changes with time, since the waste mass electrical properties change, therefore modifying the loading of the microwave cavity.
- thermal power produced in the cavity depends on the filling material properties, relative permittivity (e r ), conductivity ( ⁇ J), geometry of the cavity and type of excitation, and is calculated from:
- FIG. 9 shows the simulated magnitude of the electric field for single-waveguide-port excitation of a cavity completely filled with high and low permittivity and loss materials.
- FIG. 9A shows the simulated cavity with dimensions labeled.
- the simulated results are shown for a cavity completely filled with an effective food waste material (high loss) and for lower electrical loss plastic materials.
- the feed is an S-band (WR340) waveguide port with a lower edge 13 cm above the bottom of the cavity. From FIG. 9, it can be seen that the higher permittivity lossy loading has poor penetration depth (see FIG. 9C), while the loading with lower permittivity loss results in much higher field values and more penetration (see FIG. 9B). This indicates that, for an efficient process, the system will have to adapt to the different feed stocks.
- the fields can be found using a full-wave electromagnetic (EM) solver given a specific geometry, electrical properties, and excitation. It is worth noting that the magnetic component of the electromagnetic field has a small effect on heating since the magnetic properties/loss of the waste load are usually negligible compared to the dielectric ones/loss.
- EM electromagnetic
- Hydrothermal carbonization is carried out mainly to produce a solid product similar to coal starting from wet biomass feedstock. Though it is most effective with wet biomass, HTC has been successfully applied to municipal solid waste and plastics. Removing carboxyl and hydroxy (-OH) groups reduces the oxygen-to-carbon ratio significantly to make the final product more energy dense.
- the solid yield from this process roughly varies between 35% and 65% of the initial dry feedstock with a higher heating value (HHV) around 13-30 MJ/kg depending on the initial energy content of the feedstock. A feedstock with 75-90% moisture content is considered ideal for this process.
- HTC consists of three processes, namely, dehydration, decarboxylation, and decarbonylation, for which pretreatment or drying of the feedstock waste is not needed.
- thermal insulation may be used, in certain embodiments.
- the electrical and chemical processes that occur when there is an electromagnetic field inside a material are linked through the heating rate caused by Joule losses as: where p is the mass density of the filling material, c is the specific heat of the material, T is the temperature at a specific point within the material, and K is the thermal conductivity.
- An analytical solution for the heating rate is complicated since the temperature and electric field are functions of position. Therefore, multi-physics simulations were used to determine the temperature increase due to Joule losses and account for the anticipated energy leakage through the cavity walls with specific thermal insulation as shown in FIG. 11.
- FIG. 11 shows the image of thermal simulation setup and a side cut of the insulation.
- the cavity walls are 1mm thick tin-plated steel, the reflective surrounding has a reflectivity of 94%, and the foam insulation is 1-inch thick expanded polystyrene (XPS).
- XPS 1-inch thick expanded polystyrene
- the setup may be placed inside a second metal enclosure for safety and additional thermal insulation. Note that the waste feed stock is subjected to pressure on the order of 20 bar.
- An example of a coaxial cavity is shown in FIG. 4.
- the center conductor is implemented as an auger which has three functions: to form the cavity with many EM modes, to mix the modes mechanically, and to mix the electric field distribution.
- the RF power is first generated using an efficient oscillator, then amplified through efficient saturated gain stages and delivered to the output power stage. Since linearity is not a specification for the heating application, solid-state GaN circuits can be designed with efficiencies exceeding 80% at the lower power levels. Multiple-level power combining is investigated as a means to increase overall efficiency. Circuit-level combining is limited by combiner loss for a larger number of devices. To maximize efficiency in the present embodiments, power may be combined at the circuit level and via spatial combining within the cavity. Spatial combining has been demonstrated to maintain combining efficiency in plane-wave combiners and over-moded waveguide horn combiners. At the cavity level, the waste mass heating will result in a variable load to the probe, and thus the output-state power amplifiers (PA), which can result in reduced efficiency and instabilities.
- PA output-state power amplifiers
- the standard approach to dealing with load mismatch is to use isolators or impedance tuners at the output of the power amplifier. These devices can also be controlled adaptively in a closed loop.
- the performance of the tuners such as insertion loss and adaptation speed, typically degrades as the range of load reflection coefficient increases.
- the type of tuning device has been limited to lossy p-i-n diodes at higher power levels. For a larger tuning range, the number of tuning elements increases, therefore increasing insertion loss. In the present embodiments, out-phasing of two or more PAs is used.
- Outphasing is traditionally used to maintain efficiency for high peak-to-average power ratio (PAPR) signals by feeding two amplifiers with a constant-envelope signal, varying their relative phase to change the combined amplitude at the output.
- PAPR peak-to-average power ratio
- the reactive impedances presented to the two PAs are complex conjugates.
- a tunable Chireix-type combiner can be designed to address load impedance variations instead of signal amplitude variations (PAPR). This architecture requires a very simple tuner with only two tunable elements which handle half of the output power with a small required tuning range.
- the DC supply to the PA transistor can be varied to produce RF power variation, which is not possibly with, for example, magnetron sources.
- This method is referred to as “supply modulation” and is used effectively for efficiency enhancement when communication signals are amplified.
- the supply modulation does not need to be fast (e.g., 100 MHz in communications systems), but can be on the order of the heating time constants, and therefore the dynamic supply (supply modulator) can be extremely efficient and not degrade the overall system efficiency while providing a means to vary the power level. Variation of the power level is crucial as waste changes properties during breakdown, and from one loading to another where materials might have dramatically different electrical properties.
- the temperature of the waste mixture may be measured throughout the volume, such as with an infrared (IR) camera and several thermocouples (see FIG. 2).
- the measured temperatures are collected as inputs to the processing unit, which then controls the phase and power delivered to the probes.
- An IR camera only penetrates a few millimeters into the waste volume due to the limited skin depth at 2.45 GHz combined with the relatively high average waste conductivity. Therefore several thermocouples may be positioned at various depths in the waste. Should this not prove sufficient for proper feedback, radiometry at microwave frequencies may be used which enables temperature measurements at depths of several centimeters, or tens of centimeters. Noteworthy, the presence of liquid water throughout the entire HTC process will strongly favor temperature homogenization.
- Frequency modulation can be done at the low-power voltage controlled oscillator.
- FIG. 12 illustrates the effect of a small change in the frequency on the fields in a simulated overmoded cavity.
- the simulations in FIG. 12 show that a small change in frequency (6 MHz) has a large effect on the field distribution (cross-sectional view) in a 2.45 GHz cavity.
- the simulation in this example is for an empty cavity. Note that frequency modulation, power modulation or power combining are straightforward with magnetron sources, while SSPAs lend themselves easily to both frequency variation and power variation.
- Load stirring is another effective means of mode mixing.
- the statistics are different and therefore combining different methods will give improved uniformity.
- a statistical approach to modeling this type of problem also showed agreement with simulation.
- metallic walls are fixed boundary conditions which enforce the tangential electric field to be zero on the walls, limiting the type of modes that exist. It has been shown that varying boundary conditions with periodic structures can improve uniformity of the B-field in high-field travelling-wave magnetic resonance imaging (MRI) bores (e.g., at 16 T and 10.5 T). This can also be applied to the electric field for volume power density uniformity, through frequency selective surfaces (FSS). In fact, these can also be electrically or mechanically variable for adaptive boundary conditions.
- MRI travelling-wave magnetic resonance imaging
- FSS frequency selective surfaces
- time-domain pulse shaping For time-domain pulse shaping, this concept is borrowed from MRI time- interleaved acquisition of modes method, which enables superposition of modes over time thus improving overall uniformity. With supply modulation, combined with FM, time-domain pulse shaping is straightforward.
- a pyrolysis reactor includes a microwave cavity configured to contain a waste mixture within an internal space and a plurality of probes that couple a corresponding plurality of drive signals into the microwave cavity to excite a plurality of cavity modes and heat the waste mixture.
- the microwave cavity has walls shaped as a cylindrical shell surrounding the internal space.
- the pyrolysis reactor further includes a linear electrical conductor surrounded by the cylindrical shell.
- the linear electrical conductor is a spindle for an auger located at least partially within the internal space, to stir the waste mixture.
- the pyrolysis reactor further includes thermal insulation surrounding the microwave cavity.
- the pyrolysis reactor further includes a heat shield between the microwave cavity and the thermal insulation.
- the pyrolysis reactor further includes at least one frequency selective surface disposed in front of at least a part of the microwave cavity and in the internal space, to surround the waste mixture.
- the pyrolysis reactor further includes an oscillator for generating a microwave signal, a plurality of solid-state power amplifiers for amplifying the microwave signal into the plurality of drive signals, and one or more variable phase shifters electrically connected to the oscillator, each of the variable phase shifters being configured to phase-shift one of the microwave signals prior to amplification in a corresponding one of the plurality of solid-state power amplifiers.
- the pyrolysis reactor further includes a plurality of sensors for measuring temperatures of the waste mixture, and a processing unit configured to (i) determine, based on measured temperatures, one or more phase-control signals and (ii) output the phase-control signals to the one or more phase-shifters to maximize power transfer to the waste mixture.
- the plurality of sensors includes a plurality of thermocouples and an infrared camera for recording a thermal image stream of the waste mixture.
- the plurality of sensors includes one or more microwave radiometers for measuring thermally-emitted electromagnetic radiation from the waste mixture.
- a method for processing a waste mixture includes coupling a plurality of drive signals into a microwave cavity to excite a plurality of cavity modes, the microwave cavity containing the waste mixture. The method further includes phase-shifting, based on a temperature of the waste mixture, one or more of the plurality of drive signals.
- the method further includes generating a microwave signal with an oscillator, splitting the microwave signal into the plurality of drive signals, and amplifying each of the plurality of drive signals into a corresponding one of a plurality of amplified signals.
- Said coupling includes coupling the plurality of amplified signals into the microwave cavity, and said phase-shifting occurs prior to said amplifying.
- the method further includes measuring the temperature of the waste mixture with a thermocouple.
- the method further includes recording a thermal image stream of the waste mixture using an infrared camera.
- the method further includes measuring thermally-emitted electromagnetic radiation from the waste mixture using a microwave radiometer.
- the method further includes stirring the waste mixture with an auger.
- the method further includes adding one or more additives to the waste mixture to increase thermal conductivity of the waste mixture.
- a system for processing a waste mixture includes a microwave power generator, a pyrolysis reactor having a plurality of microwave probes connected to the microwave power generator and configured to drive electromagnetic energy that heats the waste mixture inside the pyrolysis reactor and produce bio-oil.
- the system also includes a bio-oil upgrade element for producing a liquid fuel from the bio-oil.
- the system further includes an electric generator for at least partially powering the microwave power generator using the liquid fuel.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Processing Of Solid Wastes (AREA)
- Gasification And Melting Of Waste (AREA)
Abstract
A method for processing waste using pyrolysis reactor include generating a microwave signal; amplifying the microwave signal into a plurality of drive signals; measuring temperature of the waste; determining, based on measured temperature, at least one phase-control signal; and outputting the at least one phase-control signal to maximize power transfer to the waste.
Description
MICROWAVE-BASED PYROLYSIS REACTOR AND ASSOCIATED METHODS
RELATED APPLICATIONS
[0001] This application claims priority to U.S. Provisional Patent Application No. 63/090,460, filed October 12, 2020, the entirety of which is incorporated herein by reference.
STATEMENT REGARDING FEDERALLY
SPONSORED RESEARCH OR DEVELOPMENT
[0002] This invention was made with government support under grant number W911NF- 18-1-0203 awarded by ARMY/ARO. The government has certain rights in the invention.
BACKGROUND
[0003] Pyrolysis is the process of heating waste in an inert environment to induce thermal decomposition of the waste. This thermal decomposition changes the chemical composition of the waste, resulting in by-products with a host of industrial and commercial uses. When the waste contains organic matter, any resulting solid residue is typically high in carbon, taking the form of char. However, pyrolysis may also generate gaseous and liquid by-products, depending on the composition of the waste. Applications of pyrolysis include the conversion of biowaste to syngas and biochar, the production of coke from coal, the production of charcoal from wood, the conversion of ethane to ethylene (i.e., “cracking”), and waste management.
SUMMARY
[0004] Pyrolysis has been investigated as a feasible approach to processing municipal solid waste. However, such waste typically has a high moisture content (often in excess of 70%), which slows the heating of the waste. One way to improve the heating rate of pyrolysis is to use microwaves (i.e., electromagnetic waves in the microwave region of the electromagnetic spectrum). Water is an excellent absorber of microwaves, converting the absorbed microwaves into heat. This same principle is used in microwave ovens to heat food (through its water content) much more rapidly than through conventional ovens. Some waste materials (e.g., plastic) are fairly transparent to microwaves, allowing the microwave energy to penetrate the waste and heat it from
within. Other waste materials (e.g., food) are not as transparent to microwaves, yet may become increasingly transparent as they are heated and broken down.
[0005] In the military, current methods for waste management depend on the type of waste and platform. For example, the United States Navy is permitted to throw certain materials overboard ships (e.g., paper rags, glass, metal, food when further than twelve nautical miles from land, ground-up food waste when further than three nautical miles from shore). An incinerator using JP-5 jet fuel is used for paper, rags and wood, wasting weight and cost related to burning jet fuel to dispose of garbage. In the case of US Navy submarines, all possible waste is eliminated prior to deployment, while on-board waste is pumped or blown out. Other solutions include storing waste in frozen food lockers, burial in the field, and pyrolysis.
[0006] Thermochemical processes, pyrolysis, incineration, gasification, etc., have been used for waste management. Unlike incineration and gasification, pyrolysis does not directly process the waste for energy production, but converts it into intermediary compounds that can be used for up-conversion, fuel, or environmentally safe products that can be used for fertilization. Another process for upconverting waste materials is hydrothermal carbonization. Near- supercritical and supercritical fluid have been successfully used for carbonization, gasification, liquefaction, and upgrading of hydrocarbon resources including crude oils, microalgae, lignocellulosic biomasses, food wastes, and plastics. Combined hydrocarbon and nitrogen compounds can be successfully recovered from human biowaste.
[0007] Most of the work in the waste sector uses convection-based heating methods. However, microwave heating offers improved thermal efficiency and reaction speed. Microwave heating uses Joule losses of the electric field, combined with electrical conductivity of the waste material at GHz frequencies, to increase waste temperature. Because of the high penetration depth of electromagnetic waves in the radio-frequency spectrum, this type of heating may be confined within a volume possibly without damage or overheating of the surface, which is difficult to achieve with convection heating. This localized heating also improves system efficiency by directly producing heat inside the intended material, and therefore the heating rate is not limited due to thermal conductivity to an external heat source and the heat capacity of the material.
[0008] The present embodiments feature pyrolysis reactors that use microwaves to rapidly heat waste materials. At the heart of these pyrolysis reactors are microwave cavities within which the waste materials are located. Electromagnetic modes of the cavities are excited by
electromagnetic fields that are coupled into the cavity by one or more microwave probes (or launchers) driven by an external microwave source. The present embodiments advantageously use a number of techniques to ensure appropriate distribution of the electromagnetic energy throughout the cavity, thereby ensuring that the waste materials are rapidly and more uniformly heated (as compared to operation without these techniques). As described in more detail below, these techniques include overmoding of the cavity, outphasing, amplitude modulation, and frequency modulation. Unlike many prior-art pyrolysis reactors, the present embodiments are not adversely affected by the moisture content of the waste, and may even perform better when water is intentionally added to the waste.
[0009] The pyrolysis reactors of the present embodiments feature spatial power combining, within the cavity, of electromagnetic power from several solid-state sources. By comparison, magnetron sources (e.g., as typically used in conventional microwave ovens) are usually not power combined since it is difficult to control the relative frequency and phase. Solidstate sources do not achieve as high power as magnetrons, but with spatial power combining, high microwave power levels (e.g., up to tens of kilowatts) can be achieved inside the cavity using solid-state amplifiers. To increase efficiency, the amplifiers can be operated nonlinearly. The microwave cavity can be excited using multiple probes that are all driven by solid-state power amplifiers, which are excited by one or more microwave oscillators. Dynamic relative phase shifting of the power amplifier outputs can be used to improve heating efficiency of the waste in the cavity.
[0010] In some embodiments, a radio frequency (RF) applicator delivers electromagnetic energy to a treatment volume containing an emulsion of a hydrocarbon and a substrate, which facilitates separation of the hydrocarbon and substrate molecules into layers. Hydrocarbons and other products can then be recovered from their respective layers (e.g., see US Patent No. 7,486,248). Microwave heating has also been shown to be much faster than conventional resistance heating in hydrothermal treatments.
[0011] The present embodiments can be used to process both large and small quantities of waste mass, and are therefore scalable while maintaining high energy conversion efficiency. This scaling can be implemented via (1) selection of the cavity size and frequency, (2) microwave power density by power combining the outputs of multiple solid-state amplifiers, (3) overall power using solid-state amplifiers, (4) time-domain profile when the power is on, and (5) mode-mixing through
one or more of mechanical means, frequency modulation, and varying the cavity boundary conditions.
BRIEF DESCRIPTION OF THE DRAWINGS
[0012] FIG. 1 shows a micro wave-based pyrolysis reactor, in an embodiment.
[0013] FIG. 2 shows a micro wave-based pyrolysis reactor, in an embodiment.
[0014] FIG. 3 illustrates a microwave-based pyrolysis reactor that modulates electromagnetic power coupled to each of its probes, in an embodiment.
[0015] FIG. 4 illustrates a coaxial auger in a microwave cavity of one microwave-based pyrolysis reactor for stirring waste, according to an embodiment.
[0016] FIGS. 5 and 6 collectively illustrate a microwave-based pyrolysis reactor and a frequency- selective surface, in an embodiment.
[0017] FIG. 7 is a flowchart illustrating a method for processing waste with a pyrolysis reactor, in an embodiment.
[0018] FIG. 8 illustrates a system that processes waste with a pyrolysis reactor to produce liquid fuel, in an embodiment.
[0019] FIG. 9A shows a simulated microwave cavity with dimensions used for calculation.
[0020] FIG. 9B shows calculated magnitude of electric field inside the cavity of FIG. 9A containing low permittivity mixed-density polyethylene.
[0021] FIG. 9C shows calculated magnitude of electric field inside the cavity of FIG. 9A containing high permittivity food mixture.
[0022] FIG. 10 shows simulated electric field distribution within a cylindrical microwave cavity that includes 17 probes.
[0023] FIG. 11 shows a simulation setup for thermal distribution calculation.
[0024] FIG. 12 shows the effect of a small frequency shift (6 MHz) in the field distribution in an empty microwave cavity in a simulation.
DETAILED DESCRIPTION
[0025] FIG. 1 is a perspective view of a microwave-based pyrolysis reactor 100 that uses electromagnetic energy to induce thermal breakdown of a waste mass 102. Waste mass 102 may include one or more of several types of waste, such as biowaste (e.g., food scraps, vegetation,
animal waste), wood-based products (e.g., paper, wood), metals (e.g., aluminum), Styrofoam, plastic, crude oils, microalgae, and lignocellulosic biomasses. Advantageously, waste mass 102 may contain liquids, such as water, that rapidly absorb electromagnetic energy in the microwave region of the electromagnetic spectrum, and increase the speed with which waste mass 102 is heated. An output chute 104 may be used to collect solid and liquid byproducts as they form and drop to the bottom of pyrolysis reactor 100. Gaseous byproducts may be collected with a pump 142 that evacuates an inner volume 112 of pyrolysis reactor 100 via a pump port 106. Examples of gaseous byproducts include particulate matter, volatile organic compounds, polynuclear aromatic hydrocarbons, methane, ammonia, carbon monoxide, hydrogen sulfide, hydrogen cyanide, and sulfur oxides. While waste mass 102 is shown in FIG. 1 as a rectangular prism, it may alternatively have a different shape, provided that it fits within inner volume 112.
[0026] Pyrolysis reactor 100 includes a microwave cavity 110 formed by electrically conductive walls 114 that surround inner volume 112. Electrically conductive walls 114 may be made of metal (e.g., copper, silver, gold, aluminum, etc.). Microwave cavity 110 supports a plurality of electromagnetic modes that store electromagnetic energy when excited. In FIG. 1, microwave cavity 110 is a cylinder in which the conductive walls 114 form a cylindrical shell having a length in the z direction (see right-handed coordinate system 150) and a radius in the transverse x-y plane. However, microwave cavity 110 may have a different geometry without departing from scope hereof. For example, microwave cavity 110 may be shaped as a rectangular cuboid, a square cuboid, or another type of hollow three-dimensional prism.
[0027] Microwaves are coupled into the microwave cavity 110 through one or more probes 122, each driven by a corresponding amplifier 120. In the example of FIG. 1, first and second probes 122(1), 122(2) couple electromagnetic energy into the microwave cavity 110, where waste mass 102 absorbs the electromagnetic energy, converting it to heat that increases the temperature of waste mass 102 and results in breakdown of waste mass 102. As described in more detail below, power to each amplifier 120 may be optimized to increase the amount of electromagnetic power delivered to waste mass 102, in turn increasing the speed at which waste mass 102 increases in temperature and therefore breaks down. More than two probes 122 (e.g., four, ten, twenty-eight, fifty or other number) may be used without departing from the scope hereof. Furthermore, while FIG. 1 shows first and second probes 122(1), 122(2) located on opposite sides of microwave cavity
110 (in the x direction) and at the same z position, probes 122 may be located at different positions without departing from the scope hereof.
[0028] Probes 122 are driven with an electrical microwave signal 131 that is generated by a frequency source 130 and split with a power splitter 132. Microwave signal 131 may have a single frequency selected to resonate with one of the modes of microwave cavity 110. For example, the frequency may be selected to coincide with the lowest-frequency fundamental resonance of microwave cavity 110 (when the cavity is empty, i.e., not loaded). However, to increase the spatial uniformity of the electric field within microwave cavity 110, microwave cavity 110 may be overmoded, i.e., driven at a frequency higher than that of the fundamental resonance to excite several modes. In some embodiments, microwave signal 131 contains a plurality of frequencies.
[0029] Since amplifier linearity is not a relevant specification for microwave-based pyrolysis, each amplifier 120(1), 120(2) may be a high-efficiency solid-state amplifier based on GaN or LDMOS power transistors. Each amplifier 120(1), 120(2) may output several watts of power, or more, depending on the volume and contents of waste mass 102.
[0030] The frequency of microwave signal 131 may be selected near 2.45 GHz or 900 MHz, where the electromagnetic energy has sufficient penetration depth given the electrical conductivity of most waste materials. Therefore, the use of these frequencies may help ensure uniform heating and even thermal breakdown throughout all of waste mass 102. In some embodiments, the frequency of microwave signal 131 lies within the Industrial, Scientific, and Medical (ISM) band between 2.4 and 2.5 GHz. In these embodiments, each amplifier 120(1), 120(2) may be based on GaN power transistors. In other embodiments, the frequency of microwave signal 131 lies within the ISM band between 915 and 928 MHz. In these embodiments, each amplifier 120(1), 120(2) may be based on either GaN power transistors or LDMOS power transistors However, in general, the frequency of microwave signal 131 is not limited to only these bands, provided that the cavity is shielded.
[0031] Given that pyrolysis reactor 100 may operate with powers up to tens of kilowatts, or more, operation at frequencies within ISM bands advantageously minimizes the likelihood of generating interference that can disrupt telecommunications. In some embodiments, pyrolysis reactor 100 operates at multiple frequencies simultaneously. For example, first probe 122(1) may be driven near the ISM band at 915 MHz, while second probe 122(2) is driven near the ISM band at 2.45 GHz. The use of multiple frequencies can help ensure uniform heating given the different
absorption properties of materials within waste mass 102, and how these absorption properties change as the waste mass 102 breaks down. Additional ISM bands are centered at 5.8 GHz, 24.125 GHz, 61.25 GHz, 433.92 MHz, 40.68 MHz, etc. Additional probes 122 may be driven at frequencies within these additional ISM bands to further increase the frequency diversity of the electric field within microwave cavity 110. Since the number of transverse-electric (TE) and transverse-magnetic (TM) modes within the microwave cavity 110 scales as f3, where f is the frequency of the microwave signal 131, operating microwave cavity 110 at higher frequencies can advantageously facilitate overmoding. However, a higher frequency usually results in a lower efficiency of solid-state amplifiers 120, and less penetration of the waste due to a smaller skin depth. Thus, there is a trade-off between overmoding and efficiency that can be evaluated based on the design requirements.
[0032] FIG. 2 is a perspective view of a microwave-based pyrolysis reactor 200 that uses time-varying outphasing to increase the efficiency with which power is coupled out of amplifiers 120(1), 120(2) and into waste mass 102. Pyrolysis reactor 200 is similar to pyrolysis reactor 100 of FIG. 1 except that it includes a signal processing module 210 that controls a variable phase shifter 214 with a phase-control signal 208 to change the relative phase A between first and second drive signals 206(1), 206(2) that are fed to first and second amplifiers 120(1), 120(2), respectively. The relative phase A is selected to maximize constructive interference between the electromagnetic fields near waste mass 102, which in turn maximizes the power density and thus absorption by waste mass 102. Additionally, outphasing can improve amplifier efficiency when the load is varying.
[0033] To determine the relative phase A , signal processing module 210 monitors waste mass 102 to determine how microwave properties (e.g., real and imaginary components of the permittivity) change as waste mass 102 heats and breaks down. Thus, waste mass 102 may be thought of as a microwave load that varies spatially and temporally. To determine changes in the microwave load, signal processing module 210 may use a plurality of thermocouples 212 to record temperatures of waste mass 102 at various positions, both at the surface of waste mass 102 and inside waste mass 102. Signal processing module 210 may additionally or alternatively use one or more infrared cameras (e.g., infrared camera 207 as shown) to record a temperature distribution of waste mass 102. Infrared camera 207 may view waste mass 102 via a viewport 204. Signal processing module 210 processes this temperature data to determine the optimum phase shift A ,
and then outputs corresponding phase-control signal 208. Signal processing module 210 may operate as part of a feedback loop.
[0034] In one embodiment, pyrolysis reactor 200 uses radiometry at microwave frequencies to measure the properties of waste mass 102 at depths of several centimeters. This embodiment advantageously overcomes limitations of infrared camera 207, which can only detect the temperature of waste mass 102 to within a few millimeters of its surface. Radiometry may also provide a greater density of spatial temperature measurements than can be implemented with the plurality of thermocouples 212. In this embodiment, pyrolysis reactor 200 additionally includes a radiometer 209 for receiving the emitted black-body radiation in the microwave region of the spectrum where the skin depth in waste is comparable to the waste dimensions.
[0035] Although FIG. 2 shows pyrolysis reactor 200 with two probes 122(1), 122(2), pyrolysis reactor 200 may include a plurality of n probes 122, where n is an integer greater than or equal to 2. In general, the output of frequency source 130 is split into n drive signals 206 that are amplified by n corresponding amplifiers 120 to drive the n probes 122. Signal processing module 210 processes the temperature data to determine n — 1 optimum phase shifts A -L, ... , ^pn- for maximizing power absorbed by waste mass 102. Signal processing module 210 then outputs n — 1 corresponding phase-control signals 208 that control corresponding n — 1 variable phase shifters 214. Since only relative shifts need to be controlled for outphasing, one of the n drive signals 206 does not need to be phase shifted.
[0036] FIG. 3 illustrates how micro wave-based pyrolysis reactor 200 of FIG. 2 can be additionally configured to modulate the electromagnetic power coupled to each of probes 122. For clarity of illustration, thermocouples 212, infrared camera 207, and variable phase shifter 214 are not shown in FIG. 3. Signal processing module 210 processes received temperature data to determine n amplitudes, or power levels, at which each the n probes 122 should be driven to control the power absorbed by waste mass 102 in addition to outphasing. Advantageously, variation of the power levels throughout the pyrolysis process can be used to maintain high efficiency as the electrical properties of waste mass 102 changes as it breaks down. Such a variation in power levels is difficult to implement in a conventional magnetron-based microwave reactor.
[0037] As shown in FIG. 3, each amplifier 120(1), 120(2) includes a power amplifier 320(1), 320(2) driven by a corresponding driver amplifier 322(1), 322(2). The main purpose of
each driver amplifier 322 is gain, not efficiency. However, if the gain of the corresponding power amplifier 320 is low, then the efficiency of driver amplifier 322 affects overall efficiency. Each power amplifier 320 and driver amplifier 322 is powered by a DC power supply 326 via a corresponding modulator 324. Each modulator 324 is controlled via a corresponding modulation signal 326 to change the power outputted by corresponding amplifier 320, 322. In some embodiments, only power amplifiers 320(1), 320(2) are modulated. In other embodiments, both driver amplifiers 322(1), 322(2) and power amplifiers 320(1), 320(2) are modulated. Each amplifier 120(1), 120(2) may include additional stages than shown in FIG. 3, and each of these additional stages may be similarly modulated. While FIG. 3 shows pyrolysis reactor 200 with n = 2 probes 122 and 2n = 4 modulators 324, pyrolysis reactor 200 may have a different integer number n of probes 122 and k * n modulators (where k is the number of stages used for each amplifier 120) without departing from the scope hereof.
[0038] To improve electric field uniformity inside microwave cavity 110, some embodiments use frequency modulation to implement mode mixing in microwave cavity 110. When microwave cavity 110 is overmoded, a small change in the microwave frequency can greatly change the electric field distribution within the microwave cavity 110. FIG. 2 shows one example of frequency modulation, wherein frequency source 130 is a voltage-controlled oscillator driven with a frequency-control signal 218 that changes the frequency of microwave signal 131. Frequency-control signal 218 may be generated by signal -processing module 210, as shown in FIG. 2, in response to certain detected temperatures, temperature gradients, or temperature distributions. Alternatively, frequency-control signal 218 may be generated by a circuit separate from signal-processing module 210. Frequency-control signal 218 may be a periodic signal (e.g., sine wave, triangle wave, sawtooth) such that the frequency modulation is periodic. In this case, waste mass 102 responds to a time-averaged electric field at each spatial point within microwave cavity 110, where the time averaging is over one period of frequency— control signal 218. To further enhance spatial uniformity, frequency— control signal 218 may be random (e.g., white noise) or include a random component (e.g., a triangle wave superimposed with white noise).
[0039] FIG. 4 is a side view of a microwave-based pyrolysis reactor 400 that is similar to pyrolysis reactors 100, 200 of FIGS. 1 and 2, except that it uses a coaxial microwave cavity 410 instead of a hollow microwave cavity. A mixing auger 422 serves as a linear electrical conductor (hereinafter a “center” conductor) of the coaxial microwave cavity 410, and may be made of metal
with high electrical conductivity (e.g., copper, silver, aluminum, etc.). Mixing auger 422 includes one or more helical paddles 426 attached to a spindle 424 that is rotated by a motor 412. As mixing auger 422 rotates, paddles 426 mix waste mass 102 to help insure thermal uniformity of waste mass 110. For clarity of illustration, waste mass 102 is not shown in FIG. 4.
[0040] In some embodiments, spindle 424 is made of metal and paddles 426 are made of a non-electrically conductive material, such as ceramic, that can withstand the high temperatures achieved within pyrolysis reactor 400. Therefore, in these embodiments, only spindle 424, and not paddles 426, serves as the center conductor of coaxial microwave cavity 410. In other embodiments, paddles 426 are also made of metal and are in electrical contact with spindle 424. In these embodiments, both spindle 424 and paddles 426 serve as the center conductor of coaxial microwave cavity 410. While FIG. 4 shows pyrolysis reactor 400 with two probes 122, pyrolysis reactor 400 may have more than two probes 122 (e.g., 4, 10, 28, 50, etc.) without departing from the scope hereof.
[0041] FIGS. 5 and 6 show a micro wave-based pyrolysis reactor 500 that is similar to pyrolysis reactor 100 of FIG. 1 except that it includes a frequency-selective surface 502. Frequency-selective surface 502 is mounted in front of electrically conductive wall 514, which may be electrically grounded, to form microwave cavity 510 (similar to microwave cavity 110 in earlier figures). As described below, frequency-selective surface 502 may be configured to appear as an inductive, capacitive, or resonant surface. As a result, the tangential electric field of the cavity’s modes do not need to equal zero at frequency-selective surface 502 (unlike electrically conductive wall 514, where the tangential electric field always equal zero). Maxwell’s equations can be solved for the electric and magnetic field distributions of the modes satisfying this modified boundary condition. In general, the field distributions of these modes will differ from those for microwave cavity 510 without the frequency-selective surface 502. Thus, frequency- selective surface 502 provides a mechanism to further alter the energy distribution within inner volume 512 of cavity 510. For example, frequency-selective surface 502 may be used to create an energy distribution that is spatially more uniform, as compared to the energy distribution of the modes that are obtained when cavity 510 excludes frequency-selective surface 502.
[0042] Frequency-selective surface 502 is shown in FIG. 5 as a two-dimensional square grid of elements 504 formed on a dielectric substrate 506. In the example of FIG. 5, each element 504 is a Jerusalem cross formed from metal (e.g., copper). To prevent electrical shorting across
elements 504 (e.g., due to waste mass 102, which may be electrically conductive and splatter on frequency- selective surface 502), a dielectric overlayer may be placed on top of elements 504. Dielectric substrate 506 (and the dielectric overlayer, when included) may be flexible so that frequency- selective surface 502 can conform to the curvature of electrically conductive wall 514.
[0043] Frequency-selective surface 502 may be configured differently than shown in FIGS. 5 and 6. For example, each element 504 may be a different type of N-pole element (e.g., straight dipole, tripole, square spiral, etc.), loop-type element (e.g., three-legged loaded element, four-legged loaded element, hexagon element), plate-type element with solid interior (e.g., square, hexagon, circle, etc.), or a combination thereof. Similarly, elements 504 may be arranged in a different type of grid (e.g., hexagonal, triangular, rectangular, interlaced, closely-packed, etc.). Other design parameters (e.g., element size, spacings between neighboring elements, thickness of dielectric substrate 506, etc.) may be selected to achieve a particular boundary condition that gives a desired electric field distribution.
[0044] In FIGS. 5 and 6, frequency- selective surface 502 subtends an azimuthal angle <p with respect to a cylindrical axis 602 of microwave cavity 510, and is located a radial distance 504 in front of electrically conductive wall 514 (i.e., toward cylindrical axis 602). However, frequency- selective surface 502 may subtend a different azimuthal angle than shown. Furthermore, frequency- selective surface 502 may have a height, in the z direction, of any value less than or equal to the height of electrically conductive wall 514. In one embodiment, frequency-selective surface 502 azimuthally subtends 360° and has a height equal to that of wall 514, thereby fully covering wall 514. In some embodiments, an additional frequency-selective surface is placed over one or both of the flat circular top and bottom walls 514 of cylindrical microwave cavity 510. Similar frequency-selective surfaces may be placed in front of electrically conductive walls of a microwave cavity having a different shape. For example, when microwave cavity 510 is rectangular, one or more planar frequency-selective surfaces may be placed in front of these flat walls of the rectangular cavity 510.
[0045] In some embodiments, multiple frequency-selective panels 502 are placed in front of walls 514 of microwave cavity 510. In some embodiments, frequency- selective panels 502 with different electrical properties are used in different regions of microwave cavity 510 to account for spatial variations of waste mass 102. For example, a first frequency-selective panel 502 may be used at the top of microwave cavity 510 (in the +z direction) to create a first electric field
distribution that is matched to that portion of waste mass 102 at the top of the inner volume 512. Similar, a second frequency-selective panel 502 may be used at the middle of microwave cavity 510 to create a second electric field distribution that is matched to that portion of waste mass 102 at the middle of the inner volume 512. Finally, a third frequency-selective panel 502 may be used at the bottom of microwave cavity 510 to create a third electric field distribution that is matched to that portion of waste mass 102 at the bottom of inner volume 512. As an example of how these embodiments may be used, consider waste mass 102 as it undergoes chemical changes: the resulting char and ash may fall to the bottom of inner volume 512 (i.e., in the -z direction), where it accumulates. In this case, the third frequency- selective panel 502 may be designed to optimally heat the char and ash, while the first and/or second frequency-selective panels 502 may be designed to optimally heat that portion of waste mass 102 that has not yet been converted to char and ash.
[0046] In any of the above embodiments, water may be added to waste mass 102 within the inner volume 112, 512 to facilitate thermal conduction of heat within waste mass 102. The water may be salt water. Alternatively or additionally, small metallic particles (e.g., nanoparticles) may be added to waste mass 102 (either with or without additional water added) to enhance scattering of the electromagnetic fields throughout waste mass 102, thereby improving the uniformity with which the electromagnetic energy is absorbed by waste mass 102.
[0047] In any of the above embodiments, the microwave cavity 110, 510 may be externally surrounded with thermal shielding, for example in space 553, to reduce heat loss, thereby improving the energy efficiency of the pyrolysis reactor. For example, this thermal shielding may be made of a material having low thermal conductivity (e.g., fiberglass, ceramic, Styrofoam, plastic, etc.) to minimize convective heat loss from the microwave cavity to the surrounding environment. For similar purposes, a heat shield (e.g., aluminum foil, steel panels, ceramic thermal barriers) may be placed around the microwave cavity to reduce radiative heat loss. In some embodiments, the microwave cavity is placed within a larger vacuum system that may be evacuated to reduce convective heat loss from the microwave cavity. For example, wall 551 confines vacuum space 553, in which microwave cavity 510 is placed. Wall 551 of the larger vacuum system may be made of metal to act as heat shield.
[0048] The features described above with respect to the pyrolysis reactors 100, 200, 400, and 500 may be combined in any way without departing from the scope hereof. Specifically, the present embodiments include all combinations of: the outphasing shown in FIG. 2, the frequency
modulation shown in FIG. 2, the amplifier modulation shown in FIG. 3, the use of frequency- selective surfaces shown in FIG. 5, and overmoding. Any of these combinations may be further implemented with the mixing auger 422 to form the coaxial microwave cavity 410 of FIG. 4.
[0049] FIG. 7 is a flowchart illustrating a method 700 for processing a waste mixture using a pyrolysis reactor. Method 700 may be implemented by part or all of any of pyrolysis reactors 100, 200, 400, and 500. Method 700 includes steps 740 and 760. However, in other embodiments method 700 may further include one or more of steps 710, 720, 730, and 750. Method 700 may be implemented with a pyrolysis reactor storing a waste mass (used interchangeably with “waste mixture” herein) within an internal space of a microwave cavity. In one embodiment, method 700 includes placing the waste mass (e.g., waste mass 102 of FIG. 1) into the microwave cavity (e.g., microwave cavity 110). The waste mass may include one or more types of waste, such as biowaste (e.g., food scraps, vegetation, animal waste), wood-based products (e.g., paper, wood), metals (e.g., aluminum), Styrofoam, plastic, crude oils, microalgae, and lignocellulosic biomasses. In certain embodiments, the heating profile, as described in steps below, may be configured specifically for the types of waste present in the waste mass. For example, waste mass containing liquid, such as water, absorbs electromagnetic energy in the microwave region of the electromagnetic spectrum more rapidly and, therefore heats up faster, than waste mass with less liquid, and may require a different heating profile. In addition, to facilitate thermal conduction within the waste mass, additives may be added to the waste mass, such as one or more of water, salt water, and metal or dielectric nanoparticles.
[0050] In step 710, a microwave signal is generated with an oscillator. In one example of step 710, probes 122 of FIG. 1 are driven with microwave signal 131 that is generated by frequency source 130. In step 720, the generated microwave signal is split into a plurality of drive signals. In general, one oscillator may generate drive signals for all probes in the microwave cavity. For example, in FIG. 2, microwave signal 131 from oscillator 130 is split with power splitter 132 into the n drive signals 206, where n is an integer greater than 1. Microwave signal 131 may have a single frequency selected to resonate with one of the modes of microwave cavity 110. To increase the spatial uniformity of the electric field within microwave cavity 110, microwave cavity 110 may be overmoded, i.e., driven at a frequency higher than that of the fundamental resonance to excite multiple modes.
[0051] Step 730 includes amplifying the plurality of drive signals into a corresponding one of a plurality of amplified signals. This amplification is for example achieved using a solid-state power amplifier for each probe. In step 740, the amplified drive signals are coupled into the microwave cavity to excite a plurality of cavity modes. In one example of step 740, one or more probes 122, each driven by a corresponding amplifier 120, excites microwave modes in microwave cavity 110 (see FIG. 2). In this example, probes 122(1) and 122(2) couple electromagnetic energy into microwave cavity 110, where waste mass 102 absorbs the electromagnetic energy, converting it to thermal energy that increases the temperature of waste mass 102 and results in breakdown of waste mass 102. Multiple probes and amplifiers 122 increase the electromagnetic power delivered to waste mass 102, in turn increasing the speed at which waste mass 102 increases in temperature and therefore breaks down.
[0052] Step 750 includes measuring one or more temperatures of the waste mass. Step 750 is, for example, performed with thermocouples 212 in FIG. 2. In step 760, the temperature measurements are used to determine the relative phases for the variable phase shifters, thereby phase-shifting one or more of the plurality of drive signals. In one example of step 760, signal processing module 210 monitors waste mass 102 to determine how its microwave properties (e.g., real and imaginary components of the permittivity) change as it heats and breaks down. Thus, waste mass 102 may be thought of as a microwave load that varies spatially and temporally. To determine changes in the microwave load, signal processing module 210 may use thermocouples 212 to record temperatures of waste mass 102 at various positions, both at the surface and inside waste mass 102.
[0053] Step 750 may also include recording a thermal image stream of the waste mixture using an infrared camera. For example, infrared camera 207 records a temperature distribution of waste mass 102 through viewport 204. Infrared camera, however, penetrates only a few millimeters into the water volume due to the limited skin depth. For this reason, the image stream from the infrared camera may be used in conjunction with thermocouples 212 placed at various locations and depth of waste mass 102.
[0054] In certain embodiments, step 750 includes, instead of or in addition to the infrared camera, a microwave radiometer (e.g., radiometer 209 in FIG. 2) that measures thermally-emitted electromagnetic radiation from waste mass 102.
[0055] In step 760, at least one phase-control signal is determined based on the measured temperatures. By way of example, to determine the phase-control signal, or relative phase A< >, processing module 210 monitors the measured temperatures at various locations including at the surface and inside of waste mass 102, to determine how its microwave properties (e.g., real and imaginary components of the permittivity) change as waste mass 102 heats and breaks down. As waste mass 102 undergoes changes, the thermal load changes as a function of space and time. As a result, the relative phase is continuously updated to maintain thermal efficiency and uniformity. This process requires accurate measurements of temperature at as many locations in the cavity as possible. In certain embodiments, one or both of an infrared camera (e.g., infrared camera 207) and a microwave radiometer (e.g., radiometer 209) may be used in conjunction with the plurality of thermocouples to provide better spatial and temporal resolution of the measured temperature profile.
[0056] Additionally, in step 760, the one or more phase-control signals are outputted to a one or more corresponding variable phase-shifters. In one example of step 760, after having determined the relative phase between two probes 120(1) and 120(2) needed to maintain thermal uniformity and efficiency in cavity 110 in step 740, signal processing module 210 outputs the relative phase 208 to variable phase shifter 214 for probe 122(2). For reactors having more than two probes, only the relative phase differences among the plurality of probes are determined. Accordingly, the number of variable phase shifters, and therefore the number of phase-control signals, may be one less than the number of probes. However, a different number of phase shifters (and corresponding phase control signals) may be used without departing from the scope hereof.
[0057] From step 760, the phase-adjusted drive signal from each phase-shifter is fed into a corresponding power amplifier of step 730. Accordingly, steps 730, 740, 750 and 760 may be iterated until the waste is fully converted into one or more intermediary compounds that can be used for up-conversion, fuel, or environmentally safe products that can be used for, for example, fertilization.
[0058] Method 700 may include additional steps without departing from the scope hereof. As part of maintaining thermal uniformity of the waste mass throughout the thermochemical process, method 700 may include, for example, stirring the waste mixture with an auger located at least partially within the internal space of the microwave cavity. For example, mixing auger 422
may be rotated by motor 412 to mix waste mass 110, thereby improving thermal uniformity of waste mass 110.
[0059] Method 700 may also include additional or alternate steps to maintain an optimal level of power transfer, or heating efficiency, for efficient breakdown of waste. One such step includes improving electric field uniformity inside the microwave cavity by implementing mode mixing using frequency modulation. When the microwave cavity is overmoded, a small change in the frequency of the microwave signal can greatly change the electric field distribution within the microwave cavity. For example, in FIG. 2, frequency source 130 is a voltage-controlled oscillator driven with frequency— control signal 218 that changes the frequency of microwave signal 131. In this example, the frequency-modulation control signal 218 may be generated by signal-processing module 210 in response to certain detected temperatures, temperature gradients, or temperature distributions. The frequency-modulation control signal may also be random (e.g., white noise) or include a random component (e.g., a triangle wave superimposed with white noise) to further enhance spatial uniformity.
[0060] Additionally, to achieve and maintain a high level of field efficiency and therefore the power transfer, the steps in method 700 may be modified to accommodate design choices in hardware. For example, the cavity design may include frequency selective surfaces, as shown in FIGS. 5 and 6, to modify boundary conditions near the inner walls of the cavity. In another example, time-domain pulse shaping may be used with a DC power source to enable superposition of modes.
[0061] The pyrolysis reactor and methods described herein may be used in a system that can be scaled to process waste of any size including, for example, municipal solid waste. In such a system, any microwave pyrolysis reactor, including magnetron-based microwave reactor, has advantages over a conventional convection-based reactor, with those advantages being (1) improved thermal efficiency, leading to more rapid thermochemical process to take place and (2) improved thermal uniformity (e.g., not overheating certain parts, such as the surface of waste mass) due to high penetration depth of electromagnetic waves in the radio-frequency spectrum. However, solid-state-based microwave pyrolysis reactor disclosed herein has additional advantages over a conventional magnetron-based microwave reactor with the most important advantage being that the solid-state-based microwave pyrolysis reactor can be scaled in terms of (1) waste mass by cavity size and frequency choice, (2) microwave power density by power combining a plurality of
solid-state amplifiers, and (3) overall power by mode-mixing through mechanical, frequency and/or cavity boundary condition design. Additionally, in such a system, byproducts of the pyrolysis process can be further processed to produce liquid fuel, which in turn may at least partially power pyrolysis reactor.
[0062] More specifically, in waste processing system 800 a waste mass 802 is placed in the microwave cavity of pyrolysis reactor 810 and is processed following method 700. Dirty biooil 870 from the pyrolysis process has characteristics that vary according to the initial composition of waste mass 802. However, there are some contaminants that negatively influence the quality of the final product of the system. For example, liquid fuel 890, as the final product in system 800, may contain contaminants including nitrogen, sulfur, and metal-containing compounds. In some embodiments, waste processing system 800 includes a co-product recovery module 874 that analyzes dirty bio-oil 870 for these contaminants, and removes any such contaminants that are found. Some of the analysis techniques that may be used in co-product recovery module 874 include gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS) for compound identification and quantitation. Removal of the contaminants from dirty bio-oil 870 may involve one of more compound separation techniques, such as counter current chromatography.
[0063] In addition, depending on the biosolids pyrolyzed, dirty bio-oil can harm industrial equipment, produce hazardous emissions upon combustion, or both. Accordingly, some embodiments of the waste processing system 800 includes a microbial upgrading module 872 that uses a sequence of one or more microbial bioreactors to remove these harmful compounds, especially sulfur and nitrogen. An example bioreactor may have an established mixed culture dominated by strains of Pseudomonas, Klebsella, or other genera that metabolize contaminating nitrogen compounds. In certain embodiments, the sequence of bioreactors is optimized, such that the broadest and the highest toxic compounds in dirty bio-oil 870 are removed first. This type of optimization may prolong and enhance the stability of the biological treatment processes.
[0064] After the removal of harmful contaminants, the product of system 800 is clean biofuel. For example, dirty bio-oil 870, after having toxic and harmful contaminants removed by co-product recovery module 874 and microbial upgrading module 872, becomes the final product of system 800, i.e., liquid fuel 890. Liquid fuel 890 may be sold as clean biofuel 886.
[0065] Additionally, system 800 may recycle all or a portion of the final product to at least partially power the pyrolysis reactor. More specifically, in some embodiments, system 800 includes an electric generator 892. Electric generator 892 may use all or portion of liquid fuel 890 to generate electricity 884 that can be combined with external power source 882 and supply electricity to pyrolysis reactor 810. Accordingly, pyrolysis reactor 810 can be powered fully or partially by an external power source 882, by electric generator 892 using liquid fuel 890 or by a combination of both sources.
(1) Efficiency of waste breakdown
[0066] Commercial ashing machines typically use approximately 1200 W of power in a small cavity (e.g., 22 cm * 23 cm * 10 cm), giving about 0.24 W/cm3 of volume power density compared to a standard microwave oven (which results in approximately 0.01 W/cm3). A full calculation requires many assumptions since waste content varies and results in varied heating. For example, carbon content is converted to coke (highly caloric fuel), and waste with more carbon results in more coke mass. By-products include particulate matter, volatile organic compounds, polynuclear aromatic hydrocarbons, methane, ammonia, carbon monoxide, hydrogen sulfide, hydrogen cyanide, and sulfur oxides that can be either pumped out or used to continue the coking process. Generally, a reasonable approximation for the temperature change dT /dt is given by dT 0.239 x 10“6 ■ P dt C - where P is the power in watts, C the specific heat in cal/g, and p is the volume mass density in g/cm3.
[0067] The efficiency of incineration methods is informally quantified by the amount of diesel energy required to produce carbon-rich products from waste. In the case of microwave breakdown, the input is electrical power and the total efficiency will depend on (1) the primary electrical power source efficiency, (2) the microwave generation chain efficiency, and (3) the efficiency of power delivery to the waste mass over time. For the purposes of waste breakdown, a rate efficiency can be defined as:
where V is the volume of the mixed waste (making it difficult to define mass), P is the power in watts required to heat the waste, and T is the time required to reach an average temperature T. We control power and time separately, but one can also quantify it in terms of energy (e.g., joules). This definition of rate efficiency scales in volume.
(2) Heat delivery to waste mass
[0068] The input power in the rate efficiency 77 is the electrical power delivered to the microwave source. The heat energy dissipated in the waste mass can be expressed as:
where a(x, y, z, t, T is the non-uniform waste conductivity, which is a function of temperature and therefore time. The total electric field magnitude is also a function of position within the waste volume and changes with time, since the waste mass electrical properties change, therefore modifying the loading of the microwave cavity. Some relevant values that can be used in initial simulations for possible non-metallic waste are given in Table 1.
[0069] An example of the approach for predicting the thermal power is shown next. The thermal power produced in the cavity depends on the filling material properties, relative permittivity (er), conductivity (<J), geometry of the cavity and type of excitation, and is calculated from:
[0070] It is desirable to keep the power density of Joule losses uniform through the heating process because that will usually result in the best time-average efficiency. Several rectangular and
cylindrical cavities with volumes ranging from 0.0008 to 0.15 m3 were compared using a full-wave eigenmode solver (Ansys HFSS) to determine the modal content around the operating frequency of 2.4 GHz. With a single waveguide port excitation used for the simulation there is a tradeoff between large volumes which can have a high level of field uniformity and small volumes which are effectively heated with a single feed. The cavity has the shape of an actual trash-can, cylindrical in shape and with one basis larger, as shown in FIG. 9. FIG. 9 shows the simulated magnitude of the electric field for single-waveguide-port excitation of a cavity completely filled with high and low permittivity and loss materials. FIG. 9A shows the simulated cavity with dimensions labeled. FIG. 9B shows the calculated electric field magnitude for low-density polyethylene (LDPE) and polystyrene with sr = 2.25 and tan 6 = 0.0003, and FIG. 9C shows the calculated electric field magnitude for a food mixture with sr = 42 and tan 6 = 0.3, where the field value is normalized to a 1 W incident power at 2.45 GHz at the waveguide port. The simulated results are shown for a cavity completely filled with an effective food waste material (high loss) and for lower electrical loss plastic materials. For the simulations, the radii of the bases are chosen to be
= 12.7 cm and R2 = 11.2 cm, and the height is chosen to be H = 28.2 cm, as shown in FIG. 9A. The feed is an S-band (WR340) waveguide port with a lower edge 13 cm above the bottom of the cavity. From FIG. 9, it can be seen that the higher permittivity lossy loading has poor penetration depth (see FIG. 9C), while the loading with lower permittivity loss results in much higher field values and more penetration (see FIG. 9B). This indicates that, for an efficient process, the system will have to adapt to the different feed stocks.
[0071] The equation above for thermal power can be simplified if the waste volume is assumed to consist of sub-volumes that have uniform conductivities, where the integral becomes a sum:
The fields can be found using a full-wave electromagnetic (EM) solver given a specific geometry, electrical properties, and excitation. It is worth noting that the magnetic component of the electromagnetic field has a small effect on heating since the magnetic properties/loss of the waste load are usually negligible compared to the dielectric ones/loss.
(3) Hydrothermal carbonization
[0072] Hydrothermal carbonization (HTC) is carried out mainly to produce a solid product similar to coal starting from wet biomass feedstock. Though it is most effective with wet biomass, HTC has been successfully applied to municipal solid waste and plastics. Removing carboxyl and hydroxy (-OH) groups reduces the oxygen-to-carbon ratio significantly to make the final product more energy dense. The solid yield from this process roughly varies between 35% and 65% of the initial dry feedstock with a higher heating value (HHV) around 13-30 MJ/kg depending on the initial energy content of the feedstock. A feedstock with 75-90% moisture content is considered ideal for this process. HTC consists of three processes, namely, dehydration, decarboxylation, and decarbonylation, for which pretreatment or drying of the feedstock waste is not needed.
[0001] The idea remains the same, while process conditions (temperatures of 180-220°C and pressures of 20-25 bar) are intensified to speed up the process. The reaction time can vary from 1 to 72 hours based on the feedstock and desired output products. This is one of the most promising processes for waste treatment as it can handle large amount of water content. Notice how the pressure requirement is rather moderate for this process that keeps the material cost low. (4) Microwave cavity and probe design
[0073] To maximize efficiency, thermal insulation may be used, in certain embodiments. The electrical and chemical processes that occur when there is an electromagnetic field inside a material are linked through the heating rate caused by Joule losses as:
where p is the mass density of the filling material, c is the specific heat of the material, T is the temperature at a specific point within the material, and K is the thermal conductivity. An analytical solution for the heating rate is complicated since the temperature and electric field are functions of position. Therefore, multi-physics simulations were used to determine the temperature increase due to Joule losses and account for the anticipated energy leakage through the cavity walls with specific thermal insulation as shown in FIG. 11. FIG. 11 shows the image of thermal simulation setup and a side cut of the insulation. The cavity walls are 1mm thick tin-plated steel, the reflective surrounding has a reflectivity of 94%, and the foam insulation is 1-inch thick expanded polystyrene (XPS). Although not shown in FIG. 11, the setup may be placed inside a second metal enclosure for safety and additional thermal insulation. Note that the waste feed stock is subjected to pressure on the order of 20 bar. An example of a coaxial cavity is shown in FIG. 4. The center
conductor is implemented as an auger which has three functions: to form the cavity with many EM modes, to mix the modes mechanically, and to mix the electric field distribution.
(4) High-efficiency power amplifiers and power combining
[0074] The RF power is first generated using an efficient oscillator, then amplified through efficient saturated gain stages and delivered to the output power stage. Since linearity is not a specification for the heating application, solid-state GaN circuits can be designed with efficiencies exceeding 80% at the lower power levels. Multiple-level power combining is investigated as a means to increase overall efficiency. Circuit-level combining is limited by combiner loss for a larger number of devices. To maximize efficiency in the present embodiments, power may be combined at the circuit level and via spatial combining within the cavity. Spatial combining has been demonstrated to maintain combining efficiency in plane-wave combiners and over-moded waveguide horn combiners. At the cavity level, the waste mass heating will result in a variable load to the probe, and thus the output-state power amplifiers (PA), which can result in reduced efficiency and instabilities.
[0075] The standard approach to dealing with load mismatch is to use isolators or impedance tuners at the output of the power amplifier. These devices can also be controlled adaptively in a closed loop. The performance of the tuners, such as insertion loss and adaptation speed, typically degrades as the range of load reflection coefficient increases. The type of tuning device has been limited to lossy p-i-n diodes at higher power levels. For a larger tuning range, the number of tuning elements increases, therefore increasing insertion loss. In the present embodiments, out-phasing of two or more PAs is used. Outphasing is traditionally used to maintain efficiency for high peak-to-average power ratio (PAPR) signals by feeding two amplifiers with a constant-envelope signal, varying their relative phase to change the combined amplitude at the output. In the case of a non-isolated Chireix combiner, the reactive impedances presented to the two PAs are complex conjugates. A tunable Chireix-type combiner can be designed to address load impedance variations instead of signal amplitude variations (PAPR). This architecture requires a very simple tuner with only two tunable elements which handle half of the output power with a small required tuning range.
[0076] In addition to varying the phase for load-modulation, the DC supply to the PA transistor can be varied to produce RF power variation, which is not possibly with, for example, magnetron sources. This method is referred to as “supply modulation” and is used effectively for
efficiency enhancement when communication signals are amplified. In this case, however, the supply modulation does not need to be fast (e.g., 100 MHz in communications systems), but can be on the order of the heating time constants, and therefore the dynamic supply (supply modulator) can be extremely efficient and not degrade the overall system efficiency while providing a means to vary the power level. Variation of the power level is crucial as waste changes properties during breakdown, and from one loading to another where materials might have dramatically different electrical properties.
(6) Sensing and controlling the RF field distribution
[0077] The key to efficient waste heating is maintaining the electric field uniformity inside the cavity. The present embodiments combine several approaches to ensure field homogeneity for scalable pyrolysis. First, the temperature of the waste mixture may be measured throughout the volume, such as with an infrared (IR) camera and several thermocouples (see FIG. 2). The measured temperatures are collected as inputs to the processing unit, which then controls the phase and power delivered to the probes. An IR camera only penetrates a few millimeters into the waste volume due to the limited skin depth at 2.45 GHz combined with the relatively high average waste conductivity. Therefore several thermocouples may be positioned at various depths in the waste. Should this not prove sufficient for proper feedback, radiometry at microwave frequencies may be used which enables temperature measurements at depths of several centimeters, or tens of centimeters. Noteworthy, the presence of liquid water throughout the entire HTC process will strongly favor temperature homogenization.
[0078] Other approaches to maintain electric field uniformity include: (a) the use of multiple probes and variable/adaptive probe excitation phasing, which has been shown to improve field uniformity, especially as the cavity loading changes with heating; (b) various types of mode mixing such as frequency modulation (FM) and load stirring; (c) cavity design with modified wall boundary conditions through frequency selective surfaces (FSS), which can also be electrically or mechanically variable; and (d) time-domain pulse shaping can enable superposition of modes over time thus improving overall uniformity averaged over time. These approaches may be used in any combination without departing from the scope hereof.
[0079] Frequency modulation can be done at the low-power voltage controlled oscillator. FIG. 12 illustrates the effect of a small change in the frequency on the fields in a simulated overmoded cavity. The simulations in FIG. 12 show that a small change in frequency (6 MHz) has
a large effect on the field distribution (cross-sectional view) in a 2.45 GHz cavity. The simulation in this example is for an empty cavity. Note that frequency modulation, power modulation or power combining are straightforward with magnetron sources, while SSPAs lend themselves easily to both frequency variation and power variation.
[0080] Load stirring is another effective means of mode mixing. The statistics are different and therefore combining different methods will give improved uniformity. A statistical approach to modeling this type of problem also showed agreement with simulation.
[0081] For cavity design and modified boundary conditions, metallic walls are fixed boundary conditions which enforce the tangential electric field to be zero on the walls, limiting the type of modes that exist. It has been shown that varying boundary conditions with periodic structures can improve uniformity of the B-field in high-field travelling-wave magnetic resonance imaging (MRI) bores (e.g., at 16 T and 10.5 T). This can also be applied to the electric field for volume power density uniformity, through frequency selective surfaces (FSS). In fact, these can also be electrically or mechanically variable for adaptive boundary conditions.
[0082] For time-domain pulse shaping, this concept is borrowed from MRI time- interleaved acquisition of modes method, which enables superposition of modes over time thus improving overall uniformity. With supply modulation, combined with FM, time-domain pulse shaping is straightforward.
[0083] Changes may be made in the above methods and systems without departing from the scope hereof. It should thus be noted that the matter contained in the above description or shown in the accompanying drawings should be interpreted as illustrative and not in a limiting sense. The following claims are intended to cover all generic and specific features described herein, as well as all statements of the scope of the present method and system, which, as a matter of language, might be said to fall therebetween.
Combination of Features
[0084] Features described above as well as those claimed below may be combined in various ways without departing from the scope hereof. The following examples illustrate possible, non-limiting combinations of features and embodiments described above. It should be clear that other changes and modifications may be made to the present embodiments without departing from the spirit and scope of this invention:
[0085] (A) A pyrolysis reactor includes a microwave cavity configured to contain a waste mixture within an internal space and a plurality of probes that couple a corresponding plurality of drive signals into the microwave cavity to excite a plurality of cavity modes and heat the waste mixture.
[0086] (B) In the pyrolysis reactor denoted (A), the microwave cavity has walls shaped as a cylindrical shell surrounding the internal space.
[0087] (C) In the pyrolysis reactor denoted (B), the pyrolysis reactor further includes a linear electrical conductor surrounded by the cylindrical shell.
[0088] (D) In the pyrolysis reactor denoted (C), the linear electrical conductor is a spindle for an auger located at least partially within the internal space, to stir the waste mixture.
[0089] (E) In any one of the pyrolysis reactors denoted (A) to (D), the pyrolysis reactor further includes thermal insulation surrounding the microwave cavity.
[0090] (F) In the pyrolysis reactor denoted (E), the pyrolysis reactor further includes a heat shield between the microwave cavity and the thermal insulation.
[0091] (G) In any one of the pyrolysis reactors denoted (A) to (F), the pyrolysis reactor further includes at least one frequency selective surface disposed in front of at least a part of the microwave cavity and in the internal space, to surround the waste mixture.
[0092] (H) In any one of the pyrolysis reactors denoted (A) to (G), the pyrolysis reactor further includes an oscillator for generating a microwave signal, a plurality of solid-state power amplifiers for amplifying the microwave signal into the plurality of drive signals, and one or more variable phase shifters electrically connected to the oscillator, each of the variable phase shifters being configured to phase-shift one of the microwave signals prior to amplification in a corresponding one of the plurality of solid-state power amplifiers.
[0093] (I) In the pyrolysis reactor denoted (H), the pyrolysis reactor further includes a plurality of sensors for measuring temperatures of the waste mixture, and a processing unit configured to (i) determine, based on measured temperatures, one or more phase-control signals and (ii) output the phase-control signals to the one or more phase-shifters to maximize power transfer to the waste mixture.
[0094] (J) In the pyrolysis reactor denoted (I), the plurality of sensors includes a plurality of thermocouples and an infrared camera for recording a thermal image stream of the waste mixture.
[0095] (K) In the pyrolysis reactor denoted (I), the plurality of sensors includes one or more microwave radiometers for measuring thermally-emitted electromagnetic radiation from the waste mixture.
[0096] (L) A method for processing a waste mixture includes coupling a plurality of drive signals into a microwave cavity to excite a plurality of cavity modes, the microwave cavity containing the waste mixture. The method further includes phase-shifting, based on a temperature of the waste mixture, one or more of the plurality of drive signals.
[0097] (M) In the method denoted (L), the method further includes generating a microwave signal with an oscillator, splitting the microwave signal into the plurality of drive signals, and amplifying each of the plurality of drive signals into a corresponding one of a plurality of amplified signals. Said coupling includes coupling the plurality of amplified signals into the microwave cavity, and said phase-shifting occurs prior to said amplifying.
[0098] (N) In either one of the methods denoted (L) and (M), the method further includes measuring the temperature of the waste mixture with a thermocouple.
[0099] (O) In any one of the methods denoted (L) to (N), the method further includes recording a thermal image stream of the waste mixture using an infrared camera.
[0100] (P) In any one of the methods denoted (L) to (O), the method further includes measuring thermally-emitted electromagnetic radiation from the waste mixture using a microwave radiometer.
[0101] (Q) In any of the methods for processing a waste mixture denoted (L) - (P), the method further includes stirring the waste mixture with an auger.
[0102] (R) In any of the methods for processing a waste mixture denoted (L) - (Q), the method further includes adding one or more additives to the waste mixture to increase thermal conductivity of the waste mixture.
[0103] (S) A system for processing a waste mixture includes a microwave power generator, a pyrolysis reactor having a plurality of microwave probes connected to the microwave power generator and configured to drive electromagnetic energy that heats the waste mixture inside the pyrolysis reactor and produce bio-oil. The system also includes a bio-oil upgrade element for producing a liquid fuel from the bio-oil.
[0104] (T) In the system denoted (S), the system further includes an electric generator for at least partially powering the microwave power generator using the liquid fuel.
Claims
1. A pyrolysis reactor, comprising: a microwave cavity configured to contain a waste mixture within an internal space; and a plurality of probes that couple a corresponding plurality of drive signals into the microwave cavity to excite a plurality of cavity modes and heat the waste mixture.
2. The pyrolysis reactor of claim 1, the microwave cavity having walls shaped as a cylindrical shell surrounding the internal space.
3. The pyrolysis reactor of claim 2, further comprising a linear electrical conductor surrounded by the cylindrical shell.
4. The pyrolysis reactor of claim 3, wherein the linear electrical conductor is a spindle for an auger located at least partially within the internal space, to stir the waste mixture.
5. The pyrolysis reactor of claim 1, further comprising thermal insulation surrounding the micro wave cavity.
6. The pyrolysis reactor of claim 5, further comprising a heat shield between the microwave cavity and the thermal insulation.
7. The pyrolysis reactor of claim 1, further comprising at least one frequency selective surface disposed in front of at least a part of the microwave cavity and in the internal space, to surround the waste mixture.
8. The pyrolysis reactor of claim 1, further comprising: an oscillator for generating a microwave signal; a plurality of solid-state power amplifiers for amplifying the microwave signal into the plurality of drive signals; and
27
one or more variable phase shifters electrically connected to the oscillator, each of the variable phase shifters being configured to phase-shift one of the microwave signals prior to amplification in a corresponding one of the plurality of solid-state power amplifiers. The pyrolysis reactor of claim 8, further comprising: a plurality of sensors for measuring temperatures of the waste mixture; and a processing unit configured to (i) determine, based on measured temperatures, one or more phase-control signals and (ii) output the phase-control signals to the one or more phase-shifters to maximize power transfer to the waste mixture. The pyrolysis reactor of claim 9, the plurality of sensors comprising: a plurality of thermocouples; and an infrared camera for recording a thermal image stream of the waste mixture. The pyrolysis reactor of claim 9, the plurality of sensors comprising one or more microwave radiometers for measuring thermally-emitted electromagnetic radiation from the waste mixture. A method for processing a waste mixture, comprising: coupling a plurality of drive signals into a microwave cavity to excite a plurality of cavity modes, the microwave cavity containing the waste mixture; and phase-shifting, based on a temperature of the waste mixture, one or more of the plurality of drive signals. The method of claim 12, further comprising: generating a microwave signal with an oscillator; splitting the microwave signal into the plurality of drive signals; and amplifying each of the plurality of drive signals into a corresponding one of a plurality of amplified signals;
wherein: said coupling includes coupling the plurality of amplified signals into the microwave cavity; and said phase-shifting occurs prior to said amplifying. The method of claim 12, further comprising measuring the temperature of the waste mixture with a thermocouple. The method of claim 1212, further comprising recording a thermal image stream of the waste mixture using an infrared camera. The method of claim 12, further comprising measuring thermally-emitted electromagnetic radiation from the waste mixture using a microwave radiometer. The method of claim 12, further comprising stirring the waste mixture with an auger. The method of claim 12, further comprising adding one or more additives to the waste mixture to increase thermal conductivity of the waste mixture. A system for processing a waste mixture, comprising: a microwave power generator; a pyrolysis reactor having a plurality of microwave probes connected to the microwave power generator and configured to drive electromagnetic energy that heats the waste mixture inside the pyrolysis reactor and produce bio-oil; and a bio-oil upgrade element for producing a liquid fuel from the bio-oil. The system of claim 19, further comprising an electric generator for at least partially powering the microwave power generator using the liquid fuel.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP21895313.1A EP4226085A2 (en) | 2020-10-12 | 2021-10-12 | Microwave-based pyrolysis reactor and associated methods |
US18/031,337 US20240002729A1 (en) | 2020-10-12 | 2021-10-12 | Microwave-based pyrolysis reactor and associated methods |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202063090460P | 2020-10-12 | 2020-10-12 | |
US63/090,460 | 2020-10-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2022108687A2 true WO2022108687A2 (en) | 2022-05-27 |
WO2022108687A3 WO2022108687A3 (en) | 2022-06-30 |
Family
ID=81709599
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2021/054597 WO2022108687A2 (en) | 2020-10-12 | 2021-10-12 | Microwave-based pyrolysis reactor and associated methods |
Country Status (3)
Country | Link |
---|---|
US (1) | US20240002729A1 (en) |
EP (1) | EP4226085A2 (en) |
WO (1) | WO2022108687A2 (en) |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090295509A1 (en) * | 2008-05-28 | 2009-12-03 | Universal Phase, Inc. | Apparatus and method for reaction of materials using electromagnetic resonators |
IT1404132B1 (en) * | 2011-02-18 | 2013-11-15 | Cooperativa Autotrasportatori Fiorentini C A F Societa Cooperativa A R L | PRODUCTION OF HYDROCARBONS FROM RUBBER PYROLYSIS. |
EP2727647B1 (en) * | 2011-06-29 | 2020-01-15 | Microwave Chemical Co., Ltd. | Chemical reaction apparatus, and chemical reaction method |
EP3813996B1 (en) * | 2018-06-28 | 2022-09-28 | Resynergi, Inc. | Microwave system for converting hydrocarbon-based waste materials into oil and gas fuels |
-
2021
- 2021-10-12 US US18/031,337 patent/US20240002729A1/en active Pending
- 2021-10-12 EP EP21895313.1A patent/EP4226085A2/en active Pending
- 2021-10-12 WO PCT/US2021/054597 patent/WO2022108687A2/en unknown
Also Published As
Publication number | Publication date |
---|---|
EP4226085A2 (en) | 2023-08-16 |
WO2022108687A3 (en) | 2022-06-30 |
US20240002729A1 (en) | 2024-01-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Siddique et al. | Technical challenges in scaling up the microwave technology for biomass processing | |
Fernández Díez et al. | Microwave heating applied to pyrolysis | |
US20090295509A1 (en) | Apparatus and method for reaction of materials using electromagnetic resonators | |
Mehdizadeh | Microwave/RF applicators and probes: for material heating, sensing, and plasma generation | |
Ellison et al. | Investigation of microwave-assisted pyrolysis of biomass with char in a rectangular waveguide applicator with built-in phase-shifting | |
US9545609B2 (en) | Pyrolysis oil made with a microwave-transparent reaction chamber for production of fuel from an organic-carbon-containing feedstock | |
Litvak et al. | Development in Russia of megawatt power gyrotrons for fusion | |
Capodaglio et al. | Microwave-induced pyrolysis for production of sustainable biodiesel from waste sludges | |
Motasemi et al. | Microwave dielectric characterization of hay during pyrolysis | |
Motasemi et al. | Dielectric characterization of corn stover for microwave processing technology | |
Pianroj et al. | Scaled-up reactor for microwave induced pyrolysis of oil palm shell | |
WO2011019931A1 (en) | System and method using a microwave-transparent reaction chamber for production of fuel from a carbon-containing feedstock | |
Porch et al. | Microwave treatment in oil refining | |
AU2014347197A1 (en) | Char made with a microwave system | |
Komarov | A review of radio frequency and microwave sustainability-oriented technologies | |
Hu et al. | Microwave-assisted pyrolysis of waste plastics for their resource reuse: A technical review | |
Gedam et al. | Pyrolysis of municipal solid waste for syngas production by microwave irradiation | |
Vyas et al. | Review of magnetron developments | |
Li et al. | Microwave heating of biomass waste residues for sustainable bioenergy and biomass materials preparation: A parametric simulation study | |
US20240002729A1 (en) | Microwave-based pyrolysis reactor and associated methods | |
Wu et al. | Simulation and optimization of heating rate and thermal uniformity of microwave reactor for biomass pyrolysis | |
Yin | Effect of metal slots on the heating uniformity of multisource cavity microwave | |
Bosia | Low power density ion cyclotron arrays for fusion reactors | |
Jiang et al. | Numerical study on the role of microwave–metal discharge in microwave pyrolysis of WPCBs | |
CN110892789B (en) | Microwave processing apparatus |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 21895313 Country of ref document: EP Kind code of ref document: A2 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 2021895313 Country of ref document: EP Effective date: 20230512 |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 21895313 Country of ref document: EP Kind code of ref document: A2 |