CA2816195C - Hydrothermal decomposition method and apparatus for making pyrolysis liquid in the range of diesel fuel - Google Patents
Hydrothermal decomposition method and apparatus for making pyrolysis liquid in the range of diesel fuel Download PDFInfo
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- CA2816195C CA2816195C CA2816195A CA2816195A CA2816195C CA 2816195 C CA2816195 C CA 2816195C CA 2816195 A CA2816195 A CA 2816195A CA 2816195 A CA2816195 A CA 2816195A CA 2816195 C CA2816195 C CA 2816195C
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- 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
- C10G1/10—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal from rubber or rubber waste
-
- 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
- C10G1/08—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts
- C10G1/083—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal with moving catalysts in the presence of a solvent
-
- 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
- C10G2300/1011—Biomass
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Processing Of Solid Wastes (AREA)
Abstract
Conversion of organic matter to higher value hydrocarbon products comprises the step of decomposing the organic matter into liquid, char and gas in a fast catalytic hydrothermal method that has improved efficiency due to a high local energy transfer through a cavitational effect. Organic matter and catalysts are feed to a hydrothermal decomposition reactor to decompose the organic matter into gas, vapours and char that utilizes the high local energy transfer through a cavitational effect. The reactor operates at temperatures from about 200°C to 380°C with a residence time of about 1 to 60 minutes. The product is separated into a heavy slurry of char and oil, vapours and gas where the vapours are then condensed and separated into an aqueous fraction and an hydrocarbon fraction. Part of the char slurry is recycled to a cavitation chamber and excess char is outputted from the decomposition chamber.
Description
CA 2,816,195 Blakes Ref: 23009/00001 HYDROTHERMAL DECOMPOSITION METHOD AND APPARATUS FOR MAKING
PYROLYSIS LIQUID IN THE RANGE OF DIESEL FUEL
Field of the invention The present invention relates generally to a hydrothermal decomposition method and apparatus for producing organic liquid in the range of diesel fuel from biomass or other organic matter.
More particularly the invention relates to a catalytic assisted fast hydrothermal decomposition method comprising a system for the preparation of the feed and an innovative method for transferring the energy to the reaction mixture.
Background of the invention Hydrothermal decomposition treatments can be used for conversion of biomass to liquid products. In hydrothermal decomposition, also called hydrothermal liquefaction or hydrous pyrolysis, a mixture of the biomass or organic matter with some amount of water is heated in the range of 280-370 C under a pressure comprised between 10 and 25 MPa [9]. At these subcritical conditions the dramatic changes in the physical and chemical properties of water let it to act other than as solvent also as reactant and catalyst, and thus the feed can be directly converted into crude oil [10] that self-separates from excess water when conditions are returned to ambient temperature and pressure (Peterson et al. 2008).
Hydrothermal decomposition is well suited for processing high- and medium moisture (> 20%
moisture) biomass or other organic matter, since water is used as the reaction medium and thus the organic feed can be directly processed avoiding the preliminary energy consuming drying step, necessary in the case of conventional or fast pyrolysis [10].
Owing to the ability of water in subcritical conditions to carry out condensation, cleavage, and hydrolysis reactions on organic matter, significant improvements in liquid product quality were observed in comparison with pyrolysis oil, with increased carbon content, decreased oxygen content, and reduced viscosity. Furthermore, catalysts has shown to have a positive effect on the hydrothermal decomposition processes and can increase the yield of the liquid product, as well as improve its quality.
Even if generally showing better thermal stability, quality and characteristics than the pyrolysis liquid obtained from fast pyrolysis, also the crude oil obtained from hydrothermal decomposition needs to be refined and upgraded to produce an equivalent to diesel fuel for engines.
23962463.1 Date recue/Date Received 2020-08-28 CA 2,816,195 Blakes Ref: 23009/00001 Prior art Hydrothermal decomposition is generally known in the art, the research within the field has been rather extensive [A, B] and currently there is a growing interest in the hydrothermal treatments of biomasses to obtain commercially valuable liquid fuels. Notwithstanding this interest, all the hydrothermal technologies developed from the late '70 to the present had limited or no success, generally achieving the production of thick, highly oxygenated and thermally unstable liquid products that needed expensive refining and upgrading treatments to obtain a product in the range of diesel fuel. This, together with the problems inherent to operate at severe conditions, the difficulties connected with the realization of a continuous process, the low liquid yield, due to the limited dry matter content in the feed and to the low conversion rates, has hampered the commercialization of these technologies and the development of economically viable processes and commercial size plants. The numerous development projects that have been terminated without commercialization underline the difficulties.
For example, one of the first research on liquefaction was performed at the Pittsburgh Energy Research Center (PERC) in the 1970s, which led in 1977 to a pilot plant in Albany, Oregon.
Several technical problems and the low quality of the produced liquid, prevented the pilot unit from operating after 1981 [C, D].
Further, in 1982 Shell started a research aimed to the development of the HTU
(Hydrothermal Upgrading) process, but in the late eighties this research was halted and resumed in 1997 by a Dutch consortium led by Shell with support from the Dutch Government. The started R&D
program on the HTU process was targeted on the design and realization of a pilot plant, built in 2004, for obtaining data for the design of commercial plant. In the HTU pilot plant different biomasses with variable moisture content were liquefied in a range of temperatures and pressures of 300-350 C and 12-18 M Pa, respectively, and a residence time of 5-20 min [E, F].
A technical and economic feasibility study was carried out for a commercial demonstration plant capable of converting 25,000 tons of the wet organic fraction of domestic waste (dry basis)/year, that in our knowledge has not yet been built.
In the eighties, EPA's Water Engineering Research Laboratory, Cincinnati, Ohio, USA, developed a prototype sludge-to-oil reactor system (STORS) capable of processing undigested municipal sewage sludge with 20% solids at a rate of 30 L/h [G].
PYROLYSIS LIQUID IN THE RANGE OF DIESEL FUEL
Field of the invention The present invention relates generally to a hydrothermal decomposition method and apparatus for producing organic liquid in the range of diesel fuel from biomass or other organic matter.
More particularly the invention relates to a catalytic assisted fast hydrothermal decomposition method comprising a system for the preparation of the feed and an innovative method for transferring the energy to the reaction mixture.
Background of the invention Hydrothermal decomposition treatments can be used for conversion of biomass to liquid products. In hydrothermal decomposition, also called hydrothermal liquefaction or hydrous pyrolysis, a mixture of the biomass or organic matter with some amount of water is heated in the range of 280-370 C under a pressure comprised between 10 and 25 MPa [9]. At these subcritical conditions the dramatic changes in the physical and chemical properties of water let it to act other than as solvent also as reactant and catalyst, and thus the feed can be directly converted into crude oil [10] that self-separates from excess water when conditions are returned to ambient temperature and pressure (Peterson et al. 2008).
Hydrothermal decomposition is well suited for processing high- and medium moisture (> 20%
moisture) biomass or other organic matter, since water is used as the reaction medium and thus the organic feed can be directly processed avoiding the preliminary energy consuming drying step, necessary in the case of conventional or fast pyrolysis [10].
Owing to the ability of water in subcritical conditions to carry out condensation, cleavage, and hydrolysis reactions on organic matter, significant improvements in liquid product quality were observed in comparison with pyrolysis oil, with increased carbon content, decreased oxygen content, and reduced viscosity. Furthermore, catalysts has shown to have a positive effect on the hydrothermal decomposition processes and can increase the yield of the liquid product, as well as improve its quality.
Even if generally showing better thermal stability, quality and characteristics than the pyrolysis liquid obtained from fast pyrolysis, also the crude oil obtained from hydrothermal decomposition needs to be refined and upgraded to produce an equivalent to diesel fuel for engines.
23962463.1 Date recue/Date Received 2020-08-28 CA 2,816,195 Blakes Ref: 23009/00001 Prior art Hydrothermal decomposition is generally known in the art, the research within the field has been rather extensive [A, B] and currently there is a growing interest in the hydrothermal treatments of biomasses to obtain commercially valuable liquid fuels. Notwithstanding this interest, all the hydrothermal technologies developed from the late '70 to the present had limited or no success, generally achieving the production of thick, highly oxygenated and thermally unstable liquid products that needed expensive refining and upgrading treatments to obtain a product in the range of diesel fuel. This, together with the problems inherent to operate at severe conditions, the difficulties connected with the realization of a continuous process, the low liquid yield, due to the limited dry matter content in the feed and to the low conversion rates, has hampered the commercialization of these technologies and the development of economically viable processes and commercial size plants. The numerous development projects that have been terminated without commercialization underline the difficulties.
For example, one of the first research on liquefaction was performed at the Pittsburgh Energy Research Center (PERC) in the 1970s, which led in 1977 to a pilot plant in Albany, Oregon.
Several technical problems and the low quality of the produced liquid, prevented the pilot unit from operating after 1981 [C, D].
Further, in 1982 Shell started a research aimed to the development of the HTU
(Hydrothermal Upgrading) process, but in the late eighties this research was halted and resumed in 1997 by a Dutch consortium led by Shell with support from the Dutch Government. The started R&D
program on the HTU process was targeted on the design and realization of a pilot plant, built in 2004, for obtaining data for the design of commercial plant. In the HTU pilot plant different biomasses with variable moisture content were liquefied in a range of temperatures and pressures of 300-350 C and 12-18 M Pa, respectively, and a residence time of 5-20 min [E, F].
A technical and economic feasibility study was carried out for a commercial demonstration plant capable of converting 25,000 tons of the wet organic fraction of domestic waste (dry basis)/year, that in our knowledge has not yet been built.
In the eighties, EPA's Water Engineering Research Laboratory, Cincinnati, Ohio, USA, developed a prototype sludge-to-oil reactor system (STORS) capable of processing undigested municipal sewage sludge with 20% solids at a rate of 30 L/h [G].
-2-23962463.1 Date recue/Date Received 2020-08-28 CA 2,816,195 Blakes Ref: 23009/00001 STORS process was demonstrated in the nineties in Japan in a continuous plant capable of treating 5 tons of dewatered sludge per day, working at a temperature of 300 C and a pressure of 10 MPa [H].
In 2001 a STORS new demonstration plant to converted raw sewage sludge to oil, located in Colton, California, and sponsored by the United States Environmental Protection Agency, was built. The technology was further developed by the ThermoEnergy Company [I].
Using its Thermal Depolymerization technology, Changing World Technologies Inc. (CWT) in 1998 started a subsidiary, Thermo-Depolymerization Process, LLC (TDP), that in 2004 led to the realization of a large-scale plant in Carthage, Missouri, USA, capable to convert 250 tons/day of turkey offal and fats into approximately 500 barrels of fuel oil of un-reported value[L, M].
Hochschule für Angewandte VVissenschaften Hamburg, Germany (HAW) developed a technically different process named DoS (Direct liquefaction of organic Substances), that led to a semicontinuous test plant of 5 kg/h (biomass)[N, 01.
Further, the Danish company SCF Technologies developed a process to convert organic waste to oil in the presence of a homogeneous (K2CO3) and a heterogeneous (Zirconia) catalyst, at subcritical conditions (280-350 C and 22-25 MPa). The so-named CatLiq technology has been demonstrated in a 20 L/h capacity pilot plant in Copenhagen, Denmark [P].
Summary of the invention It is an object of preferred embodiments of the present invention to provide a method and apparatus, which allow for a compact and efficient hydrothermal decomposition assembly. It is a further object of preferred embodiments of the present invention to provide a method for efficiently feed and pump solid organic matter, such as chopped biomass, in the hydrothermal decomposition reactor.
In a first aspect, the invention provides a method for producing liquid hydrocarbon oil from organic matter, comprising the step of decomposing the organic matter into liquid, char and gas in a fast catalytic hydrothermal process, the method comprising the steps of:
¨ Feeding the organic matter and catalysts to a hydrothermal decomposition reactor;
In 2001 a STORS new demonstration plant to converted raw sewage sludge to oil, located in Colton, California, and sponsored by the United States Environmental Protection Agency, was built. The technology was further developed by the ThermoEnergy Company [I].
Using its Thermal Depolymerization technology, Changing World Technologies Inc. (CWT) in 1998 started a subsidiary, Thermo-Depolymerization Process, LLC (TDP), that in 2004 led to the realization of a large-scale plant in Carthage, Missouri, USA, capable to convert 250 tons/day of turkey offal and fats into approximately 500 barrels of fuel oil of un-reported value[L, M].
Hochschule für Angewandte VVissenschaften Hamburg, Germany (HAW) developed a technically different process named DoS (Direct liquefaction of organic Substances), that led to a semicontinuous test plant of 5 kg/h (biomass)[N, 01.
Further, the Danish company SCF Technologies developed a process to convert organic waste to oil in the presence of a homogeneous (K2CO3) and a heterogeneous (Zirconia) catalyst, at subcritical conditions (280-350 C and 22-25 MPa). The so-named CatLiq technology has been demonstrated in a 20 L/h capacity pilot plant in Copenhagen, Denmark [P].
Summary of the invention It is an object of preferred embodiments of the present invention to provide a method and apparatus, which allow for a compact and efficient hydrothermal decomposition assembly. It is a further object of preferred embodiments of the present invention to provide a method for efficiently feed and pump solid organic matter, such as chopped biomass, in the hydrothermal decomposition reactor.
In a first aspect, the invention provides a method for producing liquid hydrocarbon oil from organic matter, comprising the step of decomposing the organic matter into liquid, char and gas in a fast catalytic hydrothermal process, the method comprising the steps of:
¨ Feeding the organic matter and catalysts to a hydrothermal decomposition reactor;
-3-23962463.1 Date recue/Date Received 2020-08-28 CA 2,816,195 Blakes Ref: 23009/00001 ¨ decomposing the organic matter into gas, vapours and char by means of a high local energy transfer through a cavitational effect, while maintaining the bulk slurry temperature in the range of 250-350 C;
¨ separating the product into a heavy slurry of char and oil, vapours and gas;
¨ condensing the vapours;
¨ separating the vapours into an aqueous fraction and an hydrocarbon fraction;
¨ recycling part of the char slurry to the cavitation chamber;
¨ conveying the excess char outer from the decomposition reactor.
In a second aspect, the invention provides an apparatus for conveniently producing liquid hydrocarbon oil from organic matter, comprising:
¨ a system for the convenient preparation of the feed;
¨ a decomposition reactor comprising a cavitation device where the local temperature sharply increases and organic matter decomposes;
¨ an inlet through which the organic matter can be fed into the cavitation device;
¨ a vapour condenser and separator;
¨ a char conveyor for conveying the char away from the reactor.
In the present context, organic matter is to be understood as any organic material, such as plants and animals or residues thereof, such as wood, agricultural and forestry process waste materials, or industrial, human and animal waste, including plastics and petrochemical-based waste feedstock.
The term liquid hydrocarbon oil is to be understood as any organic liquid derived from a hydrothermal decomposition process, such as bio-oil or tar, the components having a boiling point in the range 20-500 C. Vapour is to be understood as any vapour derived from organic matter in a hydrothermal decomposition process, such as vaporized hydrocarbon liquid or water.
The present hydrothermal decomposition method and apparatus confer several benefits.
Thanks to the high local energy transfer through a cavitational effect no need from external heat is needed, eliminating the fouling problem of the heat exchange surfaces. The heat is given in a very effective way directly inside the organic material subject to decomposition. It is not necessary to work under high pressure because the charge is fed directly in the cavitation chamber where the conditions necessary to initiate the hydrothermal decomposition are obtained locally by the cavitation. While the bulk temperature in the decomposition reactor is maintained at temperatures in the range of 240-380 C, locally in the cavitation chamber quasi-
¨ separating the product into a heavy slurry of char and oil, vapours and gas;
¨ condensing the vapours;
¨ separating the vapours into an aqueous fraction and an hydrocarbon fraction;
¨ recycling part of the char slurry to the cavitation chamber;
¨ conveying the excess char outer from the decomposition reactor.
In a second aspect, the invention provides an apparatus for conveniently producing liquid hydrocarbon oil from organic matter, comprising:
¨ a system for the convenient preparation of the feed;
¨ a decomposition reactor comprising a cavitation device where the local temperature sharply increases and organic matter decomposes;
¨ an inlet through which the organic matter can be fed into the cavitation device;
¨ a vapour condenser and separator;
¨ a char conveyor for conveying the char away from the reactor.
In the present context, organic matter is to be understood as any organic material, such as plants and animals or residues thereof, such as wood, agricultural and forestry process waste materials, or industrial, human and animal waste, including plastics and petrochemical-based waste feedstock.
The term liquid hydrocarbon oil is to be understood as any organic liquid derived from a hydrothermal decomposition process, such as bio-oil or tar, the components having a boiling point in the range 20-500 C. Vapour is to be understood as any vapour derived from organic matter in a hydrothermal decomposition process, such as vaporized hydrocarbon liquid or water.
The present hydrothermal decomposition method and apparatus confer several benefits.
Thanks to the high local energy transfer through a cavitational effect no need from external heat is needed, eliminating the fouling problem of the heat exchange surfaces. The heat is given in a very effective way directly inside the organic material subject to decomposition. It is not necessary to work under high pressure because the charge is fed directly in the cavitation chamber where the conditions necessary to initiate the hydrothermal decomposition are obtained locally by the cavitation. While the bulk temperature in the decomposition reactor is maintained at temperatures in the range of 240-380 C, locally in the cavitation chamber quasi-
- 4 -23962463.1 Date recue/Date Received 2020-08-28 CA 2,816,195 Blakes Ref: 23009/00001 plasma conditions are reached assuring the energetic input for a fast hydrothermal decomposition. In fact, cavitation process is characterized by the formation, growth and implosive collapse of gas- or vapour-filled microbubbles in a body of liquid, where the collapse of these mecrobubbles leads to local transient temperatures and pressures over 5000 K and 1000 atm, respectively, with very high heating and cooling rates in the range of 1010 K/s. These conditions along with the presence of catalysts guarantee high liquid yields and the production of an oil containing a very limited amount of oxygen, having the characteristics of a diesel fuel.
The use of catalyst in the invention is particularly advantageous, in that it can be used in the production of a liquid hydrocarbon products that are higher in quality and more highly stable than typical thermal decomposition products. The catalyst consists essentially of or is a mixture of basic metal oxide or hydroxide and a aluminosilicate compound such as synthetic or natural zeolite. The basic metal oxide or hydroxide according to the present invention includes at least one oxide or hydroxide of at least one metal that provides a metal oxide or hydroxide having a measurable uptake of carbon dioxide upon heating.
In order to feed and pump solid organic matter to the reactor, a convenient system for the preparation of the feed is necessary. This system provides a continuous delivery of the charge to the reactor. It was found that the solid feedstock in the form of shredded materials and solid catalysts can be conveniently dispersed in a heavy oil at a ratio 1 of solid against 2 to 3 of oil.
In the preferred embodiment the obtained slurry is prepared in a horizontal blender adding hot recycled oil to the precharged feedstock and catalysts. During this step the mixture is homogenized, at a temperature of about 200 C. At this temperature the feedstock releases part of the moisture and also some light organic compounds, these products together to the air trapped in the solid bulk were conveyed to a condenser. While the gas is removed by a vacuum system, so avoiding the entrance of oxygen in the decomposition reactor, the condensed phase is injected directly in the cavitation chamber assuring part of the necessary water for the hydrothermal decomposition.
The so-prepared slurry is then extracted by a bottom screw conveyor and delivered to the cavitation chamber.
Because this part of the plant works as semi-continuous, in order to maintain continuous operation two horizontal blender are needed.
Description of the figures
The use of catalyst in the invention is particularly advantageous, in that it can be used in the production of a liquid hydrocarbon products that are higher in quality and more highly stable than typical thermal decomposition products. The catalyst consists essentially of or is a mixture of basic metal oxide or hydroxide and a aluminosilicate compound such as synthetic or natural zeolite. The basic metal oxide or hydroxide according to the present invention includes at least one oxide or hydroxide of at least one metal that provides a metal oxide or hydroxide having a measurable uptake of carbon dioxide upon heating.
In order to feed and pump solid organic matter to the reactor, a convenient system for the preparation of the feed is necessary. This system provides a continuous delivery of the charge to the reactor. It was found that the solid feedstock in the form of shredded materials and solid catalysts can be conveniently dispersed in a heavy oil at a ratio 1 of solid against 2 to 3 of oil.
In the preferred embodiment the obtained slurry is prepared in a horizontal blender adding hot recycled oil to the precharged feedstock and catalysts. During this step the mixture is homogenized, at a temperature of about 200 C. At this temperature the feedstock releases part of the moisture and also some light organic compounds, these products together to the air trapped in the solid bulk were conveyed to a condenser. While the gas is removed by a vacuum system, so avoiding the entrance of oxygen in the decomposition reactor, the condensed phase is injected directly in the cavitation chamber assuring part of the necessary water for the hydrothermal decomposition.
The so-prepared slurry is then extracted by a bottom screw conveyor and delivered to the cavitation chamber.
Because this part of the plant works as semi-continuous, in order to maintain continuous operation two horizontal blender are needed.
Description of the figures
-5-23962463.1 Date recue/Date Received 2020-08-28 CA 2,816,195 Blakes Ref: 23009/00001 Details of embodiments of the invention are described by reference to the accompanying drawings:
= Figure 1 is a schematic representation of a decomposition system for the fast catalytic assisted hydrothermal decomposition of a liquid organic feedstock employing method and apparatus of the present invention.
= Figure 2 is a drawing of one embodiments for the preparation of the slurry feed.
= Figure 3 illustrates the boiling distribution curve of the obtained hydrocarbon liquid of the process of the present invention pine sawdust feedstock.
= Figure 4 illustrates the boiling distribution curve of the obtained hydrocarbon liquid of a preferred embodiment of the present invention pine sawdust feedstock.
In the following description the corresponding elements as shown in each figure of the drawings are given the same reference number.
Referring to figures 1 and 2, solid organic matter is charged together with the catalysts in the horizontal blender (1). Once the solid material is charged the blender is sealed and the hot oil coming from the char separation system (7) or a preheated mineral oil is added. The temperature inside the blender has to be high enough to assure that the slurry releases all of the air trapped in the solid matter. The slurry is then sent by means of a pump (2) to the hydrothermal reactor (3). Due to the temperature inside the blender, moisture and some decomposition products can be released. These vapours reach a condenser (4) and the condensate is sent in the cavitation chamber.
Referring to Figures 1 and 2, the fresh charge is fed to the reactor loop at the suction of the recirculation pump (8) and injected to the cavitation chamber (2) where the temperature sharply rise and sent to the reactor drum (3). At steady-state condition the temperature in the reaction drum is in the range 250-350 C. In the reactor drum the liquid from the cavitation chamber release gas and vapours that flow to the condenser (4) where the gas are vented and the vapours condensate. The condensed liquid reach by gravity the separator (5) where they separate in two phases: a hydrocarbon phase and an aqueous phase containing some oxygenated water soluble organics. The slurries, containing the produced char that separate at the bottom of the reactor drum (3) is recycled to the cavitation chamber while a portion is extracted by the pump (6) and sent to a separation system (7) where the solid char is separated from the heavy liquid material.
In order to improve the hydrothermal decomposition in the case of dry feed, some water can be added at the entrance of the cavitation chamber.
= Figure 1 is a schematic representation of a decomposition system for the fast catalytic assisted hydrothermal decomposition of a liquid organic feedstock employing method and apparatus of the present invention.
= Figure 2 is a drawing of one embodiments for the preparation of the slurry feed.
= Figure 3 illustrates the boiling distribution curve of the obtained hydrocarbon liquid of the process of the present invention pine sawdust feedstock.
= Figure 4 illustrates the boiling distribution curve of the obtained hydrocarbon liquid of a preferred embodiment of the present invention pine sawdust feedstock.
In the following description the corresponding elements as shown in each figure of the drawings are given the same reference number.
Referring to figures 1 and 2, solid organic matter is charged together with the catalysts in the horizontal blender (1). Once the solid material is charged the blender is sealed and the hot oil coming from the char separation system (7) or a preheated mineral oil is added. The temperature inside the blender has to be high enough to assure that the slurry releases all of the air trapped in the solid matter. The slurry is then sent by means of a pump (2) to the hydrothermal reactor (3). Due to the temperature inside the blender, moisture and some decomposition products can be released. These vapours reach a condenser (4) and the condensate is sent in the cavitation chamber.
Referring to Figures 1 and 2, the fresh charge is fed to the reactor loop at the suction of the recirculation pump (8) and injected to the cavitation chamber (2) where the temperature sharply rise and sent to the reactor drum (3). At steady-state condition the temperature in the reaction drum is in the range 250-350 C. In the reactor drum the liquid from the cavitation chamber release gas and vapours that flow to the condenser (4) where the gas are vented and the vapours condensate. The condensed liquid reach by gravity the separator (5) where they separate in two phases: a hydrocarbon phase and an aqueous phase containing some oxygenated water soluble organics. The slurries, containing the produced char that separate at the bottom of the reactor drum (3) is recycled to the cavitation chamber while a portion is extracted by the pump (6) and sent to a separation system (7) where the solid char is separated from the heavy liquid material.
In order to improve the hydrothermal decomposition in the case of dry feed, some water can be added at the entrance of the cavitation chamber.
-6-23962463.1 Date recue/Date Received 2020-08-28 CA 2,816,195 Blakes Ref: 23009/00001 Examples The experiments were carried out in a continuous 100L/h pilot plant equipped with a mechanical cavitation device and fed with a slurry of sawdust and mineral oil in 1:3 weight ratio. A mixture of calcium oxide and zeolite X faujasite-type (NaX) was also used. The plant was run at the reaction temperatures indicated below. The total liquid yields and gas yields produced were indicated and in addition the characteristics of the liquid hydrocarbon product were also reported.
Example 1 Feedstock ¨ pine sawdust (dry base) = Carbon Content: 50.7%
= Hydrogen Content: 6.2%
= Oxygen Content: 39.6%
= Nitrogen Content: 1.4%
= Ash Content: 2.1%
Catalysts amount = Calcium oxide: 5% respect to the sawdust = NaX zeolite: 2% respect to the sawdust Reactor Temperature 290 C
Residence Time 10 min Run Time 8.0 hours Water 15 c/o respect to sawdust Total condensed hydrocarbon Yield: 32 %
Gas Yield: 18%
Raw water yield (from sawdust) 25%
Char yield 25%
The true boiling distillation curve of the obtained hydrocarbon liquid is shown in Figure 3.
Example 2 Feedstock ¨ pine sawdust (dry base) = Carbon Content: 50.7%
Example 1 Feedstock ¨ pine sawdust (dry base) = Carbon Content: 50.7%
= Hydrogen Content: 6.2%
= Oxygen Content: 39.6%
= Nitrogen Content: 1.4%
= Ash Content: 2.1%
Catalysts amount = Calcium oxide: 5% respect to the sawdust = NaX zeolite: 2% respect to the sawdust Reactor Temperature 290 C
Residence Time 10 min Run Time 8.0 hours Water 15 c/o respect to sawdust Total condensed hydrocarbon Yield: 32 %
Gas Yield: 18%
Raw water yield (from sawdust) 25%
Char yield 25%
The true boiling distillation curve of the obtained hydrocarbon liquid is shown in Figure 3.
Example 2 Feedstock ¨ pine sawdust (dry base) = Carbon Content: 50.7%
-7-23962463.1 Date recue/Date Received 2020-08-28 CA 2,816,195 Blakes Ref: 23009/00001 = Hydrogen Content: 6.2%
= Oxygen Content: 39.6%
= Nitrogen Content: 1.4%
= Ash Content: 2.1%
Catalysts amount = Calcium oxide: 5% respect to the sawdust = NaX zeolite: 2% respect to the sawdust Reactor Temperature 270 C
Residence Time 10 min Run Time 8.0 hours Water 10 c/o respect to sawdust Total condensed hydrocarbon Yield: 26 %
Gas Yield: 15%
Raw water yield (from sawdust) 22%
Char yield 37%
The true boiling distillation curve of the obtained hydrocarbon liquid is as shown in Figure 4.
= Oxygen Content: 39.6%
= Nitrogen Content: 1.4%
= Ash Content: 2.1%
Catalysts amount = Calcium oxide: 5% respect to the sawdust = NaX zeolite: 2% respect to the sawdust Reactor Temperature 270 C
Residence Time 10 min Run Time 8.0 hours Water 10 c/o respect to sawdust Total condensed hydrocarbon Yield: 26 %
Gas Yield: 15%
Raw water yield (from sawdust) 22%
Char yield 37%
The true boiling distillation curve of the obtained hydrocarbon liquid is as shown in Figure 4.
-8-23962463.1 Date recue/Date Received 2020-08-28
Claims (22)
1. A method for the conversion of solid organic matter to higher value hydrocarbon products, comprising the step of decomposing the solid organic matter into liquid, char and gas in a fast catalytic hydrothermal method, the method comprising the steps of:
¨ Feeding a slurry of the solid organic matter, heavy oil and catalysts to a hydrothermal decomposition reactor;
¨ decomposing the solid organic matter into gas, vapours and char in a hydrothermal decomposition reactor, by means of a high and fast local energy transfer which takes place inside a cavitation chamber; the reactor operating at a temperature from about 200 C to about 380 C and at a residence time of 1 to 60 minutes;
¨ separating the product into a heavy char slurry dispersed into heavy oil, oil, vapours and gas;
¨ condensing the vapours;
¨ separating the vapours into an aqueous fraction and an hydrocarbon fraction;
¨ recycling part of the char slurry to the cavitation chamber; and ¨ conveying the excess char out from the decomposition reactor.
¨ Feeding a slurry of the solid organic matter, heavy oil and catalysts to a hydrothermal decomposition reactor;
¨ decomposing the solid organic matter into gas, vapours and char in a hydrothermal decomposition reactor, by means of a high and fast local energy transfer which takes place inside a cavitation chamber; the reactor operating at a temperature from about 200 C to about 380 C and at a residence time of 1 to 60 minutes;
¨ separating the product into a heavy char slurry dispersed into heavy oil, oil, vapours and gas;
¨ condensing the vapours;
¨ separating the vapours into an aqueous fraction and an hydrocarbon fraction;
¨ recycling part of the char slurry to the cavitation chamber; and ¨ conveying the excess char out from the decomposition reactor.
2. The method of claim 1, wherein the solid organic matter in the hydrothermal decomposition reactor is subjected to a high local energy transfer through a cavitational effect.
3. The method of claim 1 or 2, wherein additional water is added at an entrance of the cavitation chamber.
4. The method according to any one of claims 1 to 3, wherein the residence time in the decomposition reactor is between 5 and 30 minutes.
5. The method according to any one of claims 2 to 4, wherein the cavitational energy is provided in a cavitation chamber.
23902820.3 Date Recue/Date Received 2021-03-25 CA2,816,195 Blakes Ref: 23009/00001
23902820.3 Date Recue/Date Received 2021-03-25 CA2,816,195 Blakes Ref: 23009/00001
6. The method according to claim 5, wherein the cavitation energy is provided by mechanical devices or ultrasound transducers.
7. The method according to any one of claims 1 to 6, wherein the decomposition vapors diffuse into a condenser, in which said step of condensation takes place.
8. The method according to any one of claims 1 to 7, wherein at least a portion of said char is in the form of fine solid particles, which, at the step of conveying, are conveyed away from the reactor in the form of a slurry.
9. The method according to claim 8, wherein the slurry is conveyed in a stagnant zone, in which said solid particles essentially separate from heavy organic liquids.
10. The method according to claim 9, wherein the heavy organic liquids are recycled to the decomposition reactor.
11. The method according to any one of claims 1 to 10, wherein the decomposition reactor is fed by a slurry of solid organic matter, heavy oil and catalysts.
12. The method according to claim 11 where the solid organic matter is selected from the group consisting of: plant biomass, bio-renewable fats and oils, animal biomass, organic municipal waste, sewage sludge, plastics and petrochemical-based waste feedstock.
13. The method according to claim 12, wherein the solid orgainc matter is solid particles suspended in a heavy oil.
14. The method according to claim 13, wherein the heavy oil is a product with a boiling point higher than 280 C.
15. The method according to claim 14 wherein the heavy oil is a mineral oil.
16. The method according to any one of claims 1 to 15, wherein the catalysts are selected respectively from the group of oxides and hydroxides of metal within the first 23902820.3 Date Recue/Date Received 2021-03-25 CA2,816,195 Blakes Ref: 23009/00001 and second group of the periodical system and from a group of aluminosilicate compounds.
17. The method according to claim 16 wherein the catalysts from the group of oxides and hydroxides of metal within the first and second group of the periodical system is NaOH or KOH or Ca(OH)2 or Ca0.
18. The method according to claim 16 wherein the catalysts from the group of aluminosilicate compounds is a synthetic or natural zeolite.
19. A fast hydrothermal decomposition apparatus for producing high value hydrocarbon liquid, char and gas from low value organic matter, comprising:
¨ a system for the convenient preparation of the feed;
¨ a decomposition reactor comprising a cavitation device where the local temperature sharply increases and organic matter decomposes;
¨ an inlet through which the organic matter can be fed into the cavitation device;
¨ a vapour condenser and separator; and ¨ a char conveyor for conveying the char away from the reactor.
¨ a system for the convenient preparation of the feed;
¨ a decomposition reactor comprising a cavitation device where the local temperature sharply increases and organic matter decomposes;
¨ an inlet through which the organic matter can be fed into the cavitation device;
¨ a vapour condenser and separator; and ¨ a char conveyor for conveying the char away from the reactor.
20. The apparatus according to claim 19, wherein the cavitation device is a mechanical device or an ultrasound transducer.
21. The apparatus according to claim 19 or 20, wherein the mechanical device is a pump.
22. The apparatus according to any one of claims 19 to 21, wherein the heat for the decomposition process is provided through the cavitational effect directly inside the reacting mixture without solid exchange surfaces.
23902820.3 Date Recue/Date Received 2021-03-25
23902820.3 Date Recue/Date Received 2021-03-25
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