FI20225958A1 - Method for production of synthesis gas and a reactor - Google Patents
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- FI20225958A1 FI20225958A1 FI20225958A FI20225958A FI20225958A1 FI 20225958 A1 FI20225958 A1 FI 20225958A1 FI 20225958 A FI20225958 A FI 20225958A FI 20225958 A FI20225958 A FI 20225958A FI 20225958 A1 FI20225958 A1 FI 20225958A1
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- wall
- reactor
- slag
- raw gas
- steam
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- 230000015572 biosynthetic process Effects 0.000 title claims abstract description 34
- 238000003786 synthesis reaction Methods 0.000 title claims abstract description 33
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 12
- 239000007789 gas Substances 0.000 claims abstract description 94
- 239000002893 slag Substances 0.000 claims abstract description 40
- 239000000428 dust Substances 0.000 claims abstract description 39
- 238000000034 method Methods 0.000 claims abstract description 32
- 239000001301 oxygen Substances 0.000 claims abstract description 15
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 15
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000012545 processing Methods 0.000 claims abstract description 12
- 230000003647 oxidation Effects 0.000 claims abstract description 11
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 11
- 230000001681 protective effect Effects 0.000 claims abstract description 9
- 150000001722 carbon compounds Chemical class 0.000 claims abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- 239000000306 component Substances 0.000 claims description 25
- 230000008569 process Effects 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 238000005336 cracking Methods 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 239000005864 Sulphur Substances 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 208000036366 Sensation of pressure Diseases 0.000 claims 1
- 239000010410 layer Substances 0.000 description 28
- 238000002309 gasification Methods 0.000 description 12
- 239000011269 tar Substances 0.000 description 12
- 230000035508 accumulation Effects 0.000 description 6
- 238000009825 accumulation Methods 0.000 description 6
- 238000012546 transfer Methods 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 230000001276 controlling effect Effects 0.000 description 4
- 239000004071 soot Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000001805 chlorine compounds Chemical class 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000005192 partition Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000004227 thermal cracking Methods 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 101150034533 ATIC gene Proteins 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000012824 chemical production Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000002844 continuous effect Effects 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- 230000002633 protecting effect Effects 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K1/00—Purifying combustible gases containing carbon monoxide
- C10K1/02—Dust removal
-
- 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
- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
- C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
- C10G2/32—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts
-
- 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
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
- C10G47/22—Non-catalytic cracking in the presence of hydrogen
-
- 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
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
- C10G47/36—Controlling or regulating
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
- C10J3/48—Apparatus; Plants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/46—Gasification of granular or pulverulent flues in suspension
- C10J3/48—Apparatus; Plants
- C10J3/52—Ash-removing devices
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/721—Multistage gasification, e.g. plural parallel or serial gasification stages
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/723—Controlling or regulating the gasification process
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10J—PRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
- C10J3/00—Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
- C10J3/72—Other features
- C10J3/82—Gas withdrawal means
- C10J3/84—Gas withdrawal means with means for removing dust or tar from the gas
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K1/00—Purifying combustible gases containing carbon monoxide
- C10K1/04—Purifying combustible gases containing carbon monoxide by cooling to condense non-gaseous materials
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K1/00—Purifying combustible gases containing carbon monoxide
- C10K1/04—Purifying combustible gases containing carbon monoxide by cooling to condense non-gaseous materials
- C10K1/046—Reducing the tar content
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K3/00—Modifying the chemical composition of combustible gases containing carbon monoxide to produce an improved fuel, e.g. one of different calorific value, which may be free from carbon monoxide
- C10K3/001—Modifying the chemical composition of combustible gases containing carbon monoxide to produce an improved fuel, e.g. one of different calorific value, which may be free from carbon monoxide by thermal treatment
- C10K3/003—Reducing the tar content
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Combustion & Propulsion (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Abstract
Invention relates to a method for production of synthesis gas, the method comprising following steps: - providing raw gas that contains carbon compounds and sticky components to a reactor (1) for processing of the raw gas by partial oxidation wherein oxygen and steam is added to the raw gas stream, - oxygen and steam reacts with portion of said raw gas to rise the temperature to enable melt of ash and crack of hydrocarbon compounds of the sticky components, - thickness of the protective slag/dust layer is being intermittently determined and maintained such that when the slag/dust layer thickness has accumulated to a predetermined value, the slag/dust layer is dropped to the bottom of the reactor (1) by rapping at least one of the inner panel walls (31) at a time. The invention relates also to a corresponding reactor (1).
Description
Method for production of synthesis gas and a reactor
[001] The present invention relates to a method for production of synthesis gas.
The present invention relates also to a reactor for processing of synthesis gas by partial oxidation from a raw gas containing carbon and sticky components.
[002] High temperature gasification can be used to produce raw gas for power — production and various chemical production plants. Many companies are devel- oping high temperature gasification reactors to produce raw gas for further pro- duction of synthesis gas (syngas) and further liguid fuels, using feed stocks like pyrolysis oil, torrefied wood, peat and wood dust. The aim of these processes is thus to use carbon containing feed stock to produce purified gas to a given pur- pose. Ash, soot and tar are among the components that need to be purified away from the gas.
[003] In some cases the syngas produced by primary gasification may contain significant amounts of unreacted higher molecular weight hydrocarbons which can be problematic for downstream eguipment. One example of problematic hy- — drocarbons is those commonly denoted as “tars” that condense in downstream
N eguipment potentially causing operational and efficiency issues. These problem-
N atic hydrocarbons can be further processed by secondary gasification of the hy- © drocarbon-containing syngas from a primary gasifier. This configuration is similar
O to a primary gasifier except that the feedstock to the secondary gasifier includes,
Ek 25 atleast in part, the crude syngas from the primary gasifier. A secondary gasifier
N may be used with feedstocks generated from hydrocarbon processing, such as 3 refinery off gas (that is, crude syngas is not necessarily generated from a gasifi-
N cation process). In the present description these above explained problematic
N hydrocarbons, tar, benzene C6H6, ash and/or soot that need to be purified away from the gas are called as sticky components.
[004] Regarding known technology, in an entrained flow gasification reactor the ash needs to melt, whereafter the hot gas will be cooled and liquid ash will be solidified by means of a water quench or by means of a radiant cooler. Ash +
Flux needs to form a protective layer on the hot face of refractory lining. It is reported that the refractory lining will be fast destroyed by the melt if the protec- tive ash layer will not be formed or it will be washed away. In the other hand liquid alkali metal compounds (Na and K as oxides, carbonates, hydroxides, chlorides, etc) are very aggressive and corrosive in high temperatures. However, if the ash in conventional high temperature gasification reactor will not become fully liquid, — the ash will block the reactor. Still, tar removal is needed in fluidized bed gasifi- cation processes when aiming at very clean gas for various synthesis applica- tions. Thermal cracking or tar removal is known technology itself. In thermal cracking temperatures exceed 1000°C => ash is melting on the heat transfer surfaces
[005] A prior art document US 7587995 B2 shows a synthesis gas cooler for extracting heat from synthesis gas produced by a gasification process. The syn- thesis gas cooler comprises a shell having a synthesis gas inlet and a synthesis gas outlet; a fluid-cooled flue contained within the shell for receiving the synthesis gas: fluid-cooled radiant heat transfer surface is partially extending within the flue — for cooling the synthesis gas; and means for conveying the synthesis gas from the outer flue to the outlet. The main objective in the disclosure is to transfer heat from the synthesis gas so that the ash has a reduced tendency to stick to the cooling tubes and cause deposition and plugging. The document explains that the heat transfer surface design should be based on achieving the required ab-
N 25 sorption without the use of soot blowers to clean the heat transfer surface of
N deposits which will accumulate during operation. The document explains that > based upon experience at current gasification units, an eguilibrium fouling and a absorption rate is achieved over time. It is noted that such equilibrium conditions
E are also attained in industrial and utility boilers firing similar fuels, and the perfor- © 30 mance of such boilers is quite manageable. Experiences indicates that due to slag buildup on sootblowers during service, penetration of corrosive gases, and
N breakdown of seal systems in-gas stream, removable sootblowers are unac-
N ceptable from a practical maintenance and availability standpoint. The document discloses cooled hanging partition walls within a gas cooler enclosure to maintain desired cooling of gas without cleaning the partition walls by soot blowers.
[006] An object of the invention is to provide a method for production of synthe- sis gas in which the performance is considerably improved compared to the prior art solutions.
[007] Another object of the invention is to provide a method wherein residual substances and particles can be removed from a raw gas easily and effectively.
[008] An object of the invention is to provide a reactor for processing of synthe- sis gas by partial oxidation from a raw gas containing carbon and sticky compo- nents.
[009] Objects of the invention can be met substantially as is disclosed in the independent claims and in the other claims describing more details of different embodiments of the invention.
[0010] An embodiment of the present invention is a method for production of synthesis gas, the method comprising following steps: - providing raw gas that contains carbon compounds and sticky components to a
N 20 — reactor for processing of the raw gas by partial oxidation wherein oxygen and
O steam is added to the raw gas stream, oO - oxygen and steam reacts with portion of said raw gas to rise the temperature to = enable melt of ash and crack of hydrocarbon compounds of the sticky compo- - nents,
E 25 — - reactions occuring free of catalyst for cracking of sticky components are driven 3 by hydrogen of the steam to crack complex hydrocarbons into lighter volatile hy- 3 drocarbon fractions:
O - by controlling feed of steam to the reactor, sticky components of the raw gas are decomposed and residuals accumulate as a protective slag/dust layer on an inner wall of the reactor, the reactor comprises temperature-controlled inner wall and an outer wall, being arranged in a coaxial configuration in respect to each other and where the inner wall comprises a number of water tube panel walls on a suspended support and the outer walls being fixed wall, - thickness of the protective slag/dust layer is being continuously and/or intermit- tently determined and maintained such that when the slag/dust layer thickness has accumulated to a predetermined value, the slag/dust layer is dropped to the bottom of the reactor by rapping at least one of the inner panel walls at a time.
[0011] Another embodiment of the invention is a reactor for processing of syn- thesis gas by partial oxidation from a raw gas containing carbon and sticky com- ponents, the reactor comprising: - a first intake passage for feeding the raw gas, - at least one second intake passage for feeding steam and oxygen, - an exhaust passage for exit of synthesis gas, - a- second exhaust passage for removing separated condensed and/or solidified — material, - an outer wall in a fixed configuration defining an internal space, - an inner wall assembly configured on suspended support inside the outer wall and the inner wall being formed of a number of temperature-controlled water tube panel walls, —-the outer wall and the inner wall assembly are arranged in coaxial configuration in relation to each other and a longitudinal axis of the reactor, - at least one rapping device is arranged at an upper part of the inner wall for removal of a slag/dust layer on the inner wall.
N [0012] Thus, the reactor utilizes the method to treat raw gas that contains car-
O 25 bon compounds and sticky components for processing of the raw gas by partial
O oxidation wherein oxygen and steam is added to the raw gas stream. In partial 0 oxidation oxygen and steam reacts with portion of said raw gas to rise the tem-
I perature to enable melt of ash and crack of hydrocarbon compounds of the sticky - components. Depending on the raw gas composition, the temperature should be
O 30 inarange of 1100 to 1400 °C to melt ash and crack tar. Here a gasifier upstream a of the reactor may be operated at a regular lower temperature to avoid issues
N with alkali and other corrosive components. As a conseguence, the raw gas pro- duced in the gasifier and entering the reactor contain sticky components such as tar. As the raw gas is being led to the reactor, added O./ steam reacts with por- tion of said gas to rise the temperature to about 1100 to 1400 °C, then ash melts and tar cracks. The reactions occurring free of catalyst responsible for cracking are driven by hydrogen (from steam) to crack complex hydrocarbons into lighter 5 (volatile) hydrocarbon fractions :
CwHz + Oz + steam — C,H, + H2O,, where w and z are much larger than x and y.
Free of catalyst means that there are no additional substances included or in- volved as a catalyst in the reaction. After the reaction, there are still remaining some residual substances and particles that will be captured by the temperature- — controlled inner wall of the reactor.
[0013] The aim of the present process is to maintain a controlled accumulation of residuals forming a protective slag/dust layer on the reactor walls, in the tem- perature range where the tars of the raw gas will be decomposed. Too thick slag/dust layer causes plugging of the temperature-controlled walls and thus pre- venting controllability of the process. Plugging of the reactor is prevented by rap- ping the inner walls that captures the slag/dust. However, formation of the slag/dust layer is essential to the process, otherwise raw gas purification does not happen and gas separation following the reactor will deteriorate. The accu- mulation is targeted especially on the inner wall assembly configured on sus- pended support inside the outer wall and the inner wall being formed of a number of temperature-controlled water tube panel walls, here such a single hanging sector, section or panel of the inner wall is called as an inner panel wall.
[0014] The temperature of surfaces where slag/dust is to be accumulated during
N operation should be the following:
O 25 -nolessthan 200 °C to avoid any condensation of remaining traces of tar
O - no more than 350 °C to allow effective condensation of alkali and keep corrosion 0 at bay. Temperature in the reactor may advantageously controlled so that the
I reactor has a low corrosion rate below 1 millimeter per annum when exposed to - any liguid alkali metal, sulphur or chlorine compounds, while the crack of hydro-
O 30 carbon compounds of the sticky components is still the primary factor for process a temperature within the reactor. The first ash will deposit onto the inner wall as
N solid, and as the deposit will grow its surface will be increasingly softer as its temperature will be closer to the gas temperature. The deposit growth will be interrupted by rapping the inner panel walls in certain time interval, requiring col- lect of the deposit from the bottom of the reactor. The thickness of the protective slag/dust layer is being continuously and/or intermittently determined and main- tained such that when the slag/dust layer thickness has accumulated to a prede- termined value, the slag/dust layer is dropped to the bottom of the reactor by rapping at least one of the inner panel walls at a time. The cleaning action of the hammer rely on the fact that the slag/ash in direct contact with the panel surface (200 — 350 °C) will be solid. It can be rapped off and down to the bottom of the reactor / hopper only at the boundary layer between deposit and inner wall when — the boundary layer temperature is cooled enough. Rapping breaks the bond and drops the deposits in lumps/sheets which are bulky enough not to have time to melt again while falling down to the hopper. Immediately after the rapping, a new slag/dust layer starts to accumulate on the surfaces of the inner wall.
[0015] According to an embodiment, the rapping device is a spring hammer.
When considering the cleaning up of the heat transfer surfaces i.e. the inner wall, the spring hammer based technology has found to be the most efficient one in this solution. In this invention the inner wall comprising a number of inner panel walls are of hanging type and cleaned by spring hammers. This is very efficient also in operation, if needed, the changing of hanging inner walls is easy and not — very time consuming. Naturally in maintenance operations, the most time-con- suming part is a cooling down procedure of the reactor so that the reactor or possibly its enclosure, heat shield, pressure shell or like can be safely opened.
[0016] One objective of the present invention is to produce synthesis gas that
N fits easily to various following processes. If the gasification temperature in the
S 25 — reactor is under melting temperature of the ash, but over 1100 *C, the ash will
O become soft or become to hemispherical state. If the chemical composition of 0 ash is on the area of more alkaline, the ash won't totally melt in the reactor when z the gasification temperature is under 1400 *C. According to the experiments on - the invention, the gasification temperature range of 1100°C - 1300°C is suitable
O 30 for producing low tar containing gas. That brings one desired property, the pro- a duced synthesis gas by the method can be cooled down to +5°C - +20°C without
N problems. Cooling of the synthesis gas to low temperatures is typically needed because following the water wash for removing ammonium, chlorides etc. and because possible compression. Chlorine removal may be needed for further pro- cessing and to protect shift-conversion catalyst. After shift conversion the most widely used process is so called Rectisol-process. This physical wash will re- move CO. and sour gases from synthesis gas quite well. It is commonly known that Rectisol-process is a physical wash that may handle many hydrocarbons (ex. methane) and i.e. a small amount of tars in the gas are no problem in the
Rectisol-process.
[0017] According to an embodiment of the invention the thickness of the protect- ing layer of the slag/dust on inner walls of the reactor is controlled by rapping the inner walls in sequence so that the temperature of the water/steam inside the inner walls is maintained within desired range. Thus, the thickness of slag/dust layer is determined by calculation based on temperature difference between in- going and outcoming water/steam of the inner panel walls.
[0018] According to an embodiment of the invention the slag/dust layer is dropped to the bottom of the reactor by rapping each one of the inner panel walls at a predetermined time interval. The intention for this action is that when the slag/dust layer is dropped to the bottom of the reactor by rapping only one or part of the inner panel walls at a predetermined time interval, the accumulation in other inner panel walls is still in another phase of the cycle. For illustrative exam- — ple, if the accumulation time for fully grown slag/dust layer is one hour and there are six separate inner panel walls, it gives a theoretical interval of ten minutes to rapp one inner panel wall while the other inner panel walls are at different state of accumulation. This makes the process much more stable when not all the inner
N panel walls are rapped at the same time. &
S 25 [0019] By controlling an insulating thickness of the slag/dust layer on the inner © wall, the cracking of sticky components in the reactor is being kept in balance.
N Also part of possible alkali metal, sulphur and/or chlorine components are being = removed from the process as attached to the slag/dust. The accumulation of the 8 slag/dust layer is not necessarily linear but it can as well be logarithmic or expo-
D 30 — nential depending on the process parameters. Therefore, it is advisable to have
O different tools to decide on the time interval for rapping the inner walls. The con- trolling of the insulating thickness or value or mass is one of those possible tools.
[0020] The fore explained provides a for a method for production of synthesis gas which performance is considerably improved.
[0021] Regarding the reactor construction, the outer wall is in a fixed configura- tion defining an internal space. According to an embodiment also the outer wall being formed of a number of temperature-controlled water tube panel walls. Pref- erably the outer wall is being formed of 6, 7, 8, 9, or more water tube panel walls having substantially planar cross section and joined together to form a continu- ous array of panels. Preferably the outer wall is gas tight.
[0022] The inner wall assembly is configured on suspended support inside the outer wall and the inner wall being formed of a number of temperature-controlled water tube panel walls, here referred as inner panel walls. Preferably the inner wall is being formed of 6, 7, 8, 9, or more inner panel walls having substantially planar cross section. Each inner panel wall is hanging on its own suspended support and thus forming an array of inner panel walls. According to an embodi- ment, the inner wall is having the same number of inner panel walls as the outer wall.
[0023] According to an embodiment, the inner wall and the outer wall are tem- perature controllable by means of fluid temperature inside the inner and outer walls. Water and steam are among the most suitable fluids for controlling the temperature of the inner walls and outer walls. Those water / steam -based con- trol systems are well-known in the industry so there is less effort needed to adapt an existing control system for this purpose.
N [0024] According to an embodiment, the reactor is inside an enclosure that is
N formed as a pressure shell. However, if the pressure inside the reactor is de- 2 25 signed to be relatively low, for example less than 200 kPa, the outer wall as such
S may be sufficient to form the closed space inside the reactor. According to an = embodiment the outer wall inside the enclosure is in a fixed configuration defining
N an internal space and the outer wall being formed of a number of temperature- 3 controlled water tube panel walls, the enclosure surrounds outside the outer wall.
N 30 These form a coaxial configuration of the reactor, the inner wall forms the inner-
N most array of panels, the outer wall is in the middle and the enclosure forms the outermost layer. In an embodiment, the coaxial configuration is such that a normal of the inner wall is substantially perpendicular to the imaginary vertical axis of the reactor. Naturally, the reactor should be heat insulated in a way or another so that it would be feasible to have those operational temperatures inside the reactor without significant heat losses. There may be a heat insulated enclo- — sure, heat shield construction, pressure shell or like.
[0025] According to an embodiment, the inner wall is shorter than the outer tube panel wall. This has the effect that the inner panels are easy to rap and there are enough room below the inner wall for the slag/dust layer to be dropped.
[0026] The exemplary embodiments of the invention presented in this patent ap- plication are not to be interpreted to pose limitations to the applicability of the appended claims. The verb "to comprise" is used in this patent application as an open limitation that does not exclude the existence of also unrecited features.
The features recited in depending claims are mutually freely combinable unless otherwise explicitly stated. The novel features which are considered as charac- teristic of the invention are set forth in particular in the appended claims.
[0027] In the following, the invention will be described with reference to the ac- companying exemplary, schematic drawings, in which — Figure 1 illustrates a reactor according to an embodiment of the invention,
N Figure 2a, 2b and 2c illustrates some details of the reactor according to another
O . . .
N embodiment of the invention,
O
0 Figure 3 illustrates an application of the present invention in a larger context of - synthesis gas production. = © 25
LO
O
LO
N
N
O
N
[0028] Figure 1 depicts schematically a reactor 1 for processing of synthesis gas by partial oxidation from a raw gas containing carbon and sticky components, the reactor comprising: - an enclosure 10 formed as a shell, - a first intake passage 4 for feeding the raw gas, - at least one second intake passage 5 for feeding steam and oxygen, here the first 4 and the second intake passages 5 being combined to one intake passage 4,5, - an exhaust passage 6 for exit of synthesis gas, - a second exhaust passage 7 for removing separated condensed and/or solidi- fied material, - an outer wall 2 inside the enclosure 10 in a fixed configuration defining an inter- nal space, - an inner wall 3 assembly configured on suspended support 32 inside the outer wall 2, - at least one rapping device 8 is arranged at an upper part of the inner wall 3 for removal of a slag/dust layer on the inner wall 3, -ahopper 71 forming a base where the removed slag/dust layer may drop when the inner wall 3 is being rapped, the hopper 71 has an inclined surface that leads the condensed and/or solidified material to the proximity of the second exhaust passage 7. Preferably the second exhaust passage 7 has a gas-tight dual hatch
N arrangement (not shown in figures) that enables collecting the condensed and/or
O 25 solidified material during continuous operation of the reactor 1. In that kind of
O dual hatch arrangement one of the hatches is always closed, meaning that both 0 hatches are not open simultaneously during operation, so there is no direct con-
I nection from inside the reactor 1 to the atmosphere. a 8 [0029] Figure 2a depicts schematical side view of a reactor 1 for processing of
D 30 synthesis gas by partial oxidation from a raw gas containing carbon and sticky
O components. Figure 2b depicts a cross-section of the reactor of Fig. 1at A-A and Fig. 2c depicts an enlarged view of encircled detail of Fig. 2b. The reactor 1 comprises:
- an enclosure 10 formed as a shell, depending on the process conditions as explained above, the enclosure 10 may formed as a pressure shell or as a ther- mal insulation, - a first intake passage 4 for feeding the raw gas, - atleast one second intake passage 5 for feeding steam and oxygen, - an outer wall 2 inside the enclosure 10 in a fixed configuration defining an inter- nal space and the outer wall 2 being formed of a number of temperature-con- trolled water tube panels forming the outer panel walls 21, the panels may pref- erably be arranged as a continuous array as depicted in Fig. 2b and Fig. 2c, - an inner wall 3 assembly configured on suspended support 32 inside the outer wall 2 and the inner wall 3 being formed of a number of separate temperature- controlled water tube inner panel walls 31, the suspended support 32 enables the inner panel walls 31 to vibrate or swing when rapped, - the outer wall 2 and the inner wall 3 assembly are arranged in coaxial configu- ration in relation to each other and a longitudinal axis 9 of the reactor 1 as de- picted in cross-sectional view of Fig. 2b, - at least one rapping device 8 is arranged at an upper part of the inner wall 3 for removal of a slag/dust layer on the inner wall 3.
[0030] According to an embodiment of the invention the interior of the reactor is made of water/steam-cooled tube wall panels according to the exemplar embod- iments shown on Figs. 2a, 2b and 2c. The inner wall and outer wall may comprise e.g. 12 separate sections of wall panels, here called as outer panel wall 21 and inner panel wall, 31. The width of each panel section may be for example 0.6 m
N 25 and height 5 m. Each panel section will be separately cleanable by spring ham-
N mer rapping. The inner panel walls 31 forming the inner wall 3 are fast and easily > replaceable as these can be formed as modular spare parts. Preferably the con- a struction is made of water tubes 310, 210 having a welded fin in between each
E water tube 310 to 310 or 210 to 210. The inner wall 3 may be formed of 6, 7, 8, © 30 9, or more inner panel walls 31 having substantially planar cross section. Simi- 3 larly, the outer wall 2 is being formed of 6, 7, 8, 9, or more outer panel walls 21
N having substantially planar cross section. Preferably the inner wall 3 is having
N the same number of panels 31 as the outer wall 2 so that the spacing between the inner wall and the outer wall remains about the same or equal around the circumference of the inner wall 3/ outer wall 2.
[0031] The reactor 1 may be dimensioned according to following example. - Raw gas flow 45 Nm%/s (combustion heat of raw gas before the reactor 450 - 500 MW) - Gas pressure 25 bar (2500 kPa). -Temperature in the reactor 1300 °C - Cooling water/steam temperature is 250 °C - Gas velocity in the reactor 2 m/s. - Gas retention time in the reactor 2 s. - The total temperature controlled wall area is 40 m? - Area of the roof is 5 m? - The area of one water tube panel wall section is 5,5 m? .
[0032] If oxygen + steam will be fed to the reactor in a relation to the raw gas so that the temperature will be 1200 - 1300 °C in the reactor, the ash will become sticky and will accumulate on the wall surfaces of the reactor. The ash deposit grow or accumulates on the walls to about 100 mm thick. That would be one possible start for seguenced cleaning of wall panel sections one by one. The panels would be freely suspended from top to be efficiently rapped. The inside — surface of the inner wall 3 can be made rough for example by overlay welding (which at the same time provides additional corrosion / erosion protection). Ac- cording to testing experiences after cleaning by spring hammer, there can be left up to 5 mm thin residual ash layer on a cooled water tube panel wall. o [0033] In Fig. 3 it is presented an exemplary embodiment of the present reactor
S 25 1 and method as claimed herein as a part of a larger production chain of synthe-
LO sis gas. Upstream of the reactor there are gasifier delivering the raw gas, then
N there are sources for oxygen and steam. These are combined in the reactor as = explained here earlier. Downstream of the reactor there may be coolers, filtration, 8 washers, shift conversion, Rectisol-process, absorbents, Fischer-Tropsch -syn-
D 30 thesis, etc.
S
N [0034] While the invention has been described herein by way of examples in connection with what are, at present, considered to be the most preferred embodiments, it is to be understood that the invention is not limited to the dis- closed embodiments, but is intended to cover various combinations or modifica- tions of its features, and several other applications included within the scope of the invention, as defined in the appended claims. The details mentioned in con- nection with any embodiment above may be used in connection with another embodiment when such combination is technically feasible.
List of elements in the figures 1 reactor 10 enclosure 2 outer wall 21 outer panel wall 210 water tube 3 inner wall 31 inner panel wall 310 water tube 32 inner wall suspended support 4 first intake passage (for raw gas) 5 second intake passage (for steam and oxygen) 6 exhaus passage (for exit gas) 7 second exhaust passage (for condensed and/or solidified material)
N 71 hopper
N 25 8 rapping device 2 81 spring hammer a 9 longitudinal axis
I ja m o 00
LO
D
N 30
N
O
N
Claims (15)
1. A method for production of synthesis gas, the method comprising follow- ing steps: - providing raw gas that contains carbon compounds and sticky components to a reactor (1) for processing of the raw gas by partial oxidation wherein oxygen and steam is added to the raw gas stream, - oxygen and steam reacts with portion of said raw gas to rise the temperature to — enable melt of ash and crack of hydrocarbon compounds of the sticky compo- nents, - reactions occuring free of catalyst for cracking of sticky components are driven by hydrogen of the steam to crack complex hydrocarbons into lighter volatile hy- drocarbon fractions: - by controlling feed of steam to the reactor (1), sticky components of the raw gas are decomposed and residuals accumulate as a protective slag/dust layer on an inner wall (3) of the reactor (1), the reactor (1) comprises temperature-controlled inner wall (3) and an outer wall (2), being arranged in a coaxial configuration in respect to each other and where the inner wall (3) comprises a number of water — tube panel walls (31) on a suspended support (32) and the outer wall (2) being fixed wall (21), - thickness of the protective slag/dust layer is being continuously and/or intermit- tently determined and maintained such that when the slag/dust layer thickness 3 has accumulated to a predetermined value, the slag/dust layer is dropped to the S 25 — bottom of the reactor (1) by rapping at least one of the inner panel walls (31) at 0 a time.
= 2. The method of according to claim 1, characterized in that thickness of N the protective slag/dust layer on inner wall (3) of the reactor (1) is controlled by 3 rapping the inner wall (3) in sequence so that the temperature of the water/steam N 30 inside the inner wall (3) is maintained within desired range. N
3. The method of according to claim 1 or 2, characterized in that the slag/dust layer is dropped to the bottom of the reactor (1) by rapping at least one of the water tube panel walls (31) forming the inner wall (3) at a predetermined time interval.
4 The method of according to claim 1 or any of the preceding claims, char- acterized in that by controlling an insulating thickness of the slag/dust layer on the inner wall (3), the cracking of sticky components in the reactor (1) is being kept in balance.
5. The method of according to claim 1 or any of the preceding claims, char- acterized in that a part of possible alkali metal, sulphur and/or chlorine compo- nents are being removed from the process as attached to the slag/dust.
6. The method of according to claim 1 or any of the preceding claims, char- acterized in that the reaction in the reactor (1) is: CwHz + Oz + steam — CyHy + H2O, where w and z are larger than x and y.
7. A reactor (1) for processing of synthesis gas by partial oxidation from a raw gas containing carbon and sticky components, the reactor (1) comprising: - a first intake passage (4) for feeding the raw gas, - at least one second intake passage (5) for feeding steam and oxygen, - an exhaust passage (6) for exit of synthesis gas, -asecondexhaust passage (7) for removing separated condensed and/or solid- ified material, - an outer wall (2) in a fixed configuration defining an internal space, N - an inner wall (3) assembly configured on suspended support (32) inside the N outer wall (2) and the inner wall (3) being formed of a number of temperature- 2 25 controlled water tube panel walls (31), S - the outer wall (2) and the inner wall (3) assembly are arranged in coaxial con- = figuration in relation to each other and a longitudinal axis (9) of the reactor (1), N - at least one rapping device (8) is arranged at an upper part of the inner wall (3) 3 for removal of a slag/dust layer on the inner wall (3). N S 30
8. The reactor (1) according to claim 7, characterized in that the rapping device (8) is a spring hammer (81).
9. The reactor (1) according to claim 7 or 8, characterized in that the outer wall (2) is temperature-controlled and being formed of 6, 7, 8, 9, or more water tube panel walls (21) having substantially planar cross section.
10. The reactor (1) according to claim 7 or any of the preceding claims, char- acterized in that the inner wall (3) is being formed of 6, 7, 8, 9, or more water tube panel walls (31) having substantially planar cross section.
11. The reactor (1) according to claim 7 or any of the preceding claims, char- acterized in that the inner wall (3) is having the same number of water tube panel walls (31) as the outer wall (2).
12. The reactor (1) according to claim 7 or any of the preceding claims, char- acterized in that the inner wall (3) and the outer wall (2) are temperature control- lable by means of fluid temperature inside the inner wall (3) and outer wall (2).
13. The reactor (1) according to claim 7 or any of the preceding claims, char- acterized in that further comprising an enclosure (10) that is formed as a pres- — sure shell.
14. The reactor (1) according to claim 7, characterized in that the coaxial configuration is such that a normal of the inner wall is substantially perpendicular to the imaginary longitudinal axis (9) of the reactor (1).
15. The reactor (1) according to claim 7, characterized in that the inner wall — (3) is shorter than the outer wall (2). N N O N O 0 N I a a 00 LO O LO N N O N
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FI20225958A FI20225958A1 (en) | 2022-10-25 | 2022-10-25 | Method for production of synthesis gas and a reactor |
PCT/EP2023/078771 WO2024088822A1 (en) | 2022-10-25 | 2023-10-17 | Method for production of synthesis gas and a reactor |
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FI20225958A FI20225958A1 (en) | 2022-10-25 | 2022-10-25 | Method for production of synthesis gas and a reactor |
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Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3137586A1 (en) * | 1981-09-22 | 1983-04-07 | L. & C. Steinmüller GmbH, 5270 Gummersbach | "METHOD FOR TREATING PROCESS GASES COMING FROM A GASIFICATION REACTOR" |
DE3725424C1 (en) * | 1987-07-31 | 1988-07-21 | Steinmueller Gmbh L & C | Radiation cooler for cooling gases laden with dust |
US5980858A (en) * | 1996-04-23 | 1999-11-09 | Ebara Corporation | Method for treating wastes by gasification |
DE19829385C1 (en) | 1998-07-01 | 1999-10-28 | Krc Umwelttechnik Gmbh | Pressurised slagging gasifier for treating ash-containing carbonaceous materials |
US7587995B2 (en) | 2005-11-03 | 2009-09-15 | Babcock & Wilcox Power Generation Group, Inc. | Radiant syngas cooler |
CN101842467B (en) * | 2007-09-18 | 2013-09-25 | 犹德有限公司 | Gasification reactor and method for entrained-flow gasification |
US8475546B2 (en) | 2008-12-04 | 2013-07-02 | Shell Oil Company | Reactor for preparing syngas |
FI123354B (en) | 2010-12-20 | 2013-03-15 | Foster Wheeler Energia Oy | Arrangement and method for gasification of solid fuel |
CN108410510B (en) * | 2018-06-11 | 2023-11-14 | 宁夏神耀科技有限责任公司 | Integrated coal gasifier for ash removal of waste boiler |
EP4257660A3 (en) * | 2021-01-06 | 2024-01-03 | GIDARA Energy B.V. | Process and apparatus for producing synthesis gas through thermochemical conversion of biomass and waste materials |
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