Process for preparing syngas from liquid feedstock

JP2026534243APending Publication Date: 2026-10-14BASF SE +1
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Patent Information

Application Number
JP2026517946
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Priority Date
2023-09-22
Filing Date
2024-09-20
Publication Date
2026-10-14

AI Technical Summary

Benefits of technology

【0013】 したがって、驚くべきことに、液相中に1種以上の有機化合物を含む供給流をシンガスの調製に使用できることが見出された。さらに、副生成物として生成され得るCO2は、プロセスに再循環させることができることが見出された。CO2を再循環させることにより、O2およびH2Oの添加を低減できることが見出された。さらに、再循環されたCO2は、1種以上の有機化合物を反応ゾーンに噴霧するために使用できることが見出された。これにより、より効率的なプロセスを提供することができ、特にCOの収率を高めることができる。

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Abstract

The present invention relates to a process for preparing syngas, the process comprising: (i) preparing a first feed stream comprising a liquid phase and a gas phase, wherein the liquid phase comprises one or more organic compounds and the gas phase comprises CO2; (ii) preparing a second feed stream comprising O2 and optionally vapor; (iii) mixing the first feed stream and the second feed stream to obtain a mixed feed stream; and (iv) reacting the mixed feed stream obtained in (iii) in a reaction zone to obtain a product stream comprising H2 and CO, optionally CO2, and optionally H2O, wherein the one or more organic compounds independently comprise one or more of C, H, and optionally O, S, and N.
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Description

[Technical Field]

[0001] The present invention relates to a process for preparing syngas (also known as synthesis gas) by a partial oxidation reaction of one or more organic compounds, wherein at least a portion of the one or more organic compounds are provided in liquid form, and the partial oxidation is preferably carried out without the use of a catalyst. [Background technology]

[0002] Generally, syngas contains H2 and CO, and can also contain CO2 and / or H2O. Syngas with specific H2-CO molar ratios can be prepared as needed. The preparation of syngas is typically carried out by partial oxidation of organic compounds in the presence of one or more of O2 and / or vapor. CO2 is produced as a byproduct and can be separated from the product stream. The separated CO2 can also be recycled back into the preparation process.

[0003] International Publication No. 2015 / 090575 relates in general to methods and apparatus for producing syngas.

[0004] International Publication No. 2022 / 200532 relates to a method for producing a synthesis gas mixture containing hydrogen and carbon monoxide by non-catalytic partial oxidation of hydrocarbons in the presence of oxygen and carbon dioxide. In this method, a reaction gas containing at least hydrocarbons, a reaction gas containing oxygen, and a reaction gas containing carbon dioxide are supplied to a partial oxidation reactor and react at a temperature in the range of 1200 to 1550°C to obtain a product gas mixture containing hydrogen, carbon monoxide, and carbon dioxide, and at least a portion of the carbon dioxide is separated from the product gas mixture and supplied back to the partial oxidation reactor. This method is characterized in that the carbon dioxide supplied to the partial oxidation reactor includes additional externally introduced carbon dioxide, and a product gas mixture with a hydrogen-to-carbon monoxide molar ratio in the range of 0.8:1 to 1.6:1 is obtained in the partial oxidation reactor.

[0005] U.S. Patent No. 10435295 relates to a method for preparing liquid fuel from syngas, the method specifically comprising the steps of: preparing a waste conversion reactor having a decomposition chamber; thermally decomposing waste, including organic and inorganic waste, in the waste conversion reactor to produce high-temperature syngas from the organic material and slag from the decomposition of the inorganic waste; the waste conversion reactor comprising a submerged arc furnace or plasma torch furnace that supplies heat to the decomposition chamber for the thermal decomposition and decomposition of the organic and inorganic waste materials; and introducing the syngas into a liquid fuel synthesis system comprising one or more synthetic fuel conversion reactors, where the syngas is converted into liquid fuel. Claim 7 discloses that one or more exhaust streams from the synthetic fuel conversion reactor, including water, carbon dioxide, and tail gas, may be introduced into the waste conversion reactor.

[0006] U.S. Patent Application Publication No. 2016 / 0362355 relates to the preparation of a gasoline oil product. This product contains hydrocarbon compounds in a range corresponding to the composition of gasoline. The refining process of the dimethyl ether (DME) used reduces the supply rate and allows for smaller reactors while keeping costs down. Carbon dioxide (CO2) is separated and recycled to a gasifier, where it can be reused, stored, or used for other purposes to improve the global environment. Simultaneously, CO2 can be reacted with hydrocarbons, water vapor, etc., via a high-temperature plasma torch to produce synthesis gas (syngas) of carbon monoxide (CO) and hydrogen (H2), adjusting the hydrogen / carbon ratio of the compound synthesized with biomass or hydrocarbons and assisting subsequent chemical synthesis reactions. The final gasoline produced is of high yield and high octane rating, with low nitrogen and sulfur pollution, and possesses very "environmentally friendly" quality.

[0007] International Publication No. 2021 / 180482 discloses a process for producing synthesis gas by gasification of carbon-containing materials, preferably by plasma gasification, using a gasification gas comprising at least 2 mol% carbon dioxide and optionally at least one gas selected from steam, oxygen, hydrogen, methane, and air, in which external energy obtained from electricity is supplied to the gasification step, and the exhaust gas of this process, which contains carbon dioxide, is at least partially recycled back into the gasification step. Furthermore, the invention proposes a process for producing a synthesis gas downstream product, by which synthesis gas is produced and used as an intermediate product in a downstream synthesis process.

[0008] U.S. Patent Application Publication 2022 / 234889(A1) relates to a method for controlling syngas composition by reactor temperature. In particular, a method for producing syngas is disclosed, which involves the partial oxidation of a hydrocarbon feedstock, in which the partial oxidation is carried out under specific reaction conditions.

[0009] European Patent Application Publication No. 3878807(A1) relates to a synthesis gas production process by external heat gasification using controlled carbon dioxide reduction. In particular, a synthesis gas production process by gasification of carbon-containing materials is disclosed.

[0010] Since organic compounds exist in liquid form, a process was required to prepare syngas using one or more organic compounds in liquid form. [Prior art documents] [Patent Documents]

[0011] [Patent Document 1] International Publication No. 2015 / 090575 [Patent Document 2] International Publication No. 2022 / 200532 [Patent Document 3] U.S. Patent No. 10435295 [Patent Document 4] U.S. Patent Application Publication No. 2016 / 0362355

Patent Document 5

Patent Document 6

Patent Document 7

Summary of the Invention

Problems to be Solved by the Invention

[0012] Accordingly, it was an object to provide a process for preparing syngas that allows the processing of liquid feedstock. Furthermore, it was also an object to provide a process for preparing syngas that enables CO2 recirculation and allows reduction of the required amounts of O2 and steam. A further object was to provide a process for producing syngas from a circular liquid or circulatable liquid feedstock, which in particular achieves a neutral CO2 balance.

Means for Solving the Problems

[0013] Accordingly, it has surprisingly been found that a feed stream comprising one or more organic compounds in the liquid phase can be used for the preparation of syngas. Furthermore, it has been found that CO2 that may be produced as a by-product can be recirculated to the process. It has been found that recirculating CO2 can reduce the addition of O2 and H2O. Furthermore, it has been found that the recirculated CO2 can be used to atomize one or more organic compounds into the reaction zone. This allows a more efficient process to be provided, and in particular the yield of CO can be increased.

[0014] Accordingly, the present invention relates to a process for preparing syngas, which process comprises: (i) a step of preparing a first feed stream comprising a liquid phase and a gas phase, wherein the liquid phase comprises one or more organic compounds, and the gas phase comprises CO2; (ii) a step of preparing a second feed stream comprising O2 and optionally comprising steam; (iii) The step of mixing the first supply flow and the second supply flow to obtain a mixed supply flow, (iv)(iii) The mixed feed stream obtained in (iv)(iii) is reacted in the reaction zone to obtain a product stream containing H2 and CO, and optionally CO2, H2O, or CO2 and H2O. Includes, One or more organic compounds independently contain one or more of C, H, and optionally O, S, and N.

[0015] Preferably, 90 to 100% by weight, more preferably 95 to 100% by weight, and more preferably 99 to 100% by weight, of one or more organic compounds contained in the liquid phase of the first feed stream prepared in (i) consist of C, H, and optionally one or more O, S, and N.

[0016] Preferably, 49.5 to 100% by weight, more preferably 60 to 95% by weight, and more preferably 70 to 95% by weight of one or more organic compounds consist of C.

[0017] Preferably, 0.5 to 12% by weight, more preferably 2 to 11% by weight, and more preferably 4 to 11% by weight of one or more organic compounds consist of H.

[0018] Preferably, 0 to 50% by weight, more preferably 0 to 40% by weight, more preferably 0 to 30% by weight, and more preferably 0 to 20% by weight or less of one or more organic compounds consist of oxygen.

[0019] It is preferable that 0 to 10% by weight, more preferably 0 to 6% by weight, and more preferably 0 to 4% by weight of one or more organic compounds consist of S.

[0020] It is preferable that 0 to 10% by weight, more preferably 0 to 6% by weight, and more preferably 0 to 4% by weight of one or more organic compounds consist of N.

[0021] The one or more organic compounds contained in the liquid phase are preferably selected from the group consisting of pyrolysis oil, heating oil, vacuum residue, preferably vacuum distillation residue, crude oil residue, heavy crude oil, ultra-heavy crude oil, tar sand bitumen, bisbreaker bottom residue, de-scattering equipment bottom residue, C5 asphaltene fraction, preferably C5 asphaltene, high viscosity residue, bio-oil, fuel oil, pyrolysis gasoline, tire pyrolysis oil (TPO), waste oil, used oil, and mixtures thereof, and the one or more compounds are preferably pyrolysis oils.

[0022] When one or more organic compounds contained in the liquid phase are selected from the group consisting of pyrolysis oil, heating oil, vacuum residue, preferably vacuum distillation residue, crude oil residue, heavy crude oil, ultra-heavy crude oil, tar sand bitumen, bisbreaker bottom residue, de-breaker bottom residue, C5 asphaltene fraction, preferably C5 asphaltene, high viscosity residue, bio-oil, fuel oil, pyrolysis gasoline, tire pyrolysis oil (TPO), waste oil, used oil, and mixtures thereof, the pyrolysis oil is preferably obtained from the pyrolysis of one or more of biomass, plastic waste, and mixed plastic waste, preferably mixed plastic waste, the mixed plastic waste preferably includes optionally shredded waste tires, and the mixed plastic waste more preferably includes one or more polyethylene, polypropylene, polyisoprene, poly(ethylene terephthalate), polystyrene, one or more copolymers thereof, one or more block polymers thereof, one or more graft copolymers thereof, and mixtures of two or more thereof.

[0023] Furthermore, if one or more organic compounds contained in the liquid phase are selected from the group consisting of pyrolysis oil, heating oil, vacuum residue, preferably vacuum distillation residue, crude oil residue, heavy crude oil, ultra-heavy crude oil, tar sand bitumen, bisbreaker bottom residue, de-scattering equipment bottom residue, C5 asphaltene fraction, preferably C5 asphaltene, high viscosity residue, bio-oil, fuel oil, pyrolysis gasoline, tire pyrolysis oil (TPO), waste oil, used oil, and mixtures thereof, the heating oil is (C1-C 100 ) hydrocarbons, preferably (C5-C 80)hydrocarbon, more preferably (C 10 -C 60 )hydrocarbon, more preferably (C 11 -C 40 )hydrocarbon, more preferably (C 12 -C 25 )hydrocarbon, more preferably (C 13 -C 21 )hydrocarbon, preferably (C 14 -C 20 )hydrocarbon. It is preferable to be selected from the group consisting of

[0024] The boiling point of the heating oil is preferably in the range of 100 to 1,000°C, more preferably in the range of 150 to 750°C, more preferably in the range of 200 to 500°C, more preferably in the range of 225 to 375°C, and more preferably in the range of 250 to 350°C, at a pressure in the range of 0.99 to 1.01 bara.

[0025] The one or more organic compounds preferably have a lower heating value in the range of 20 to 60 MJ / kg, more preferably in the range of 30 to 50 MJ / kg.

[0026] 90 to 100% by weight, more preferably 95 to 100% by weight, more preferably 99 to 100% by weight of the gas phase contained in the first feed stream prepared in (i) preferably consists of CO2.

[0027] The first feed stream prepared in (i) preferably has a weight ratio of the one or more organic compounds to CO2, organic compound:CO2, of 1:5 or more, more preferably in the range of 1:5 to 1000:1, more preferably in the range of 1:5 to 500:1, more preferably in the range of 1:5 to 100:1, more preferably in the range of 1:5 to 50:1, more preferably in the range of 1:1 to 25:1, more preferably in the range of 2:1 to 20:1, and more preferably in the range of 5:1 to 15:1.

[0028] It is preferable that 90 to 100% by weight, more preferably 95 to 100% by weight, and more preferably 99 to 100% by weight of the first feed stream prepared in (i) consist of one or more organic compounds and CO2.

[0029] The first supply flow prepared in (i) preferably exhibits a multiphase flow mode, more preferably a two-phase flow mode.

[0030] According to the first alternative embodiment, the first feed flow prepared in (i) exhibits a dispersed flow pattern, a plug flow pattern, a slug flow pattern, a wave flow pattern, a stratified flow pattern, an annular flow pattern, or a mist flow pattern, preferably a dispersed flow pattern, and the first feed flow prepared in (i) preferably exhibits a horizontal flow pattern.

[0031] According to the second alternative embodiment, the first feed flow prepared in (i) preferably exhibits a churn flow, annular flow, bubble flow, slug flow, or mist flow, preferably annular flow or mist flow, more preferably mist flow, and the first feed flow prepared in (i) preferably exhibits a vertical flow.

[0032] The liquid phase of the first feed stream prepared in (i) preferably has a viscosity in the range of 20 to 6,000 mPas, or more preferably in the range of 100 to 5,000 mPas, the viscosity of which is preferably determined according to Reference Example 1.

[0033] The temperature of the first feed stream prepared in (i) is preferably in the range of 50 to 220°C, more preferably in the range of 80 to 190°C, and more preferably in the range of 110 to 160°C.

[0034] The pressure of the first feed stream prepared in (i) is preferably in the range of 5 to 80 bara, more preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0035] The mass flow rate of the first feed stream prepared in (i) is preferably in the range of 100 to 20,000 kg / h, more preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0036] It is preferable that 90-100% by weight, more preferably 95-100% by weight, and more preferably 99-100% by weight of the second feed stream prepared in (ii) consist of O2.

[0037] The second feed stream prepared in (ii) preferably contains steam, and more preferably the second feed stream prepared in (ii) has a weight ratio of O2:steam calculated as element O2 to steam calculated as H2O in the range of 1:10 to 100:1, more preferably in the range of 1:1 to 61:1.

[0038] The temperature of the second feed stream prepared in (ii) is preferably in the range of 25 to 400°C, more preferably in the range of 50 to 300°C, and more preferably in the range of 90 to 250°C.

[0039] The pressure of the second supply flow prepared in (ii) is preferably in the range of 5 to 80 bara, more preferably in the range of 35 to 60 bara, and more preferably in the range of 40 to 52 bara.

[0040] The mass flow rate of the second feed stream prepared in (ii) is preferably in the range of 100 to 20,000 kg / h, more preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0041] The mixing step in (iii) is preferably carried out by spraying the first and second feed streams to form droplets and optionally liquid fragments of the liquid phase.

[0042] (iii) The mixing step is (iii.1) Preferably, the first supply flow and the second supply flow are mixed in a mixing chamber to obtain a mixed supply flow, (iii.2) The step of supplying the mixed feed stream obtained in (iii.1) to the reaction zone and Includes.

[0043] If the mixing step in (iii) includes (iii.1) and (iii.2) as defined herein, the mixing step in (iii.1) is preferably carried out by spraying the mixed feed stream to form droplets and optionally liquid fragments of the liquid phase.

[0044] Furthermore, if the mixing step in (iii) includes (iii.1) and (iii.2) as defined herein, the step of supplying the mixed feed stream to the reaction zone is preferably carried out by spraying the mixed feed stream to form droplets and optionally liquid fragments of the liquid phase.

[0045] If the mixing step in (iii.1) is performed by spraying the mixed feed stream to form droplets and, optionally, liquid fragments of the liquid phase, the spraying step is performed with a flow rate of 100-1500 m³ of the mixed feed stream. 3 Range of / h, more preferably 200~1000m 3 Preferably, the step includes applying within the range of / h.

[0046] The mixed feed flow obtained in (iii) preferably exhibits a multiphase flow mode, more preferably a two-phase flow mode.

[0047] The mixed feed flow obtained in (iii) preferably exhibits a dispersed flow pattern, a plug flow pattern, a slug flow pattern, a wave flow pattern, a stratified flow pattern, an annular flow pattern, or a mist flow pattern, preferably a dispersed flow pattern, and the mixed feed flow obtained in (iii) preferably exhibits a horizontal flow pattern.

[0048] The mixed feed flow obtained in (iii) preferably exhibits a churn flow, annular flow, bubble flow, slug flow, or mist flow, preferably annular flow or mist flow, more preferably mist flow, and the mixed feed flow obtained in (iii) preferably exhibits a vertical flow.

[0049] The mixed feed stream obtained in (iii) preferably has a weight ratio of one or more organic compounds to O2, where organic compound:O2 is in the range of 0.10:1 to 2.00:1, more preferably in the range of 0.25:1 to 1.50:1.

[0050] The mixed feed stream obtained in (iii) preferably has a weight ratio of CO2 to O2, CO2:O2, in the range of 1:500 to 1:10, more preferably in the range of 1:100 to 1:5.0, more preferably in the range of 1:75 to 1:2.0, and more preferably in the range of 1:50 to 1:1.5.

[0051] The mixed feed stream obtained in (iii) preferably has a weight ratio of one or more organic compounds to vapor, where the organic compound:vapor is in the range of 1:1 to 100:1, more preferably in the range of 5:1 to 50:1, more preferably in the range of 7:1 to 41:1, and more preferably in the range of 20:1 to 25:1.

[0052] The reaction in (iv) is preferably carried out at a temperature in the range of 1100 to 1500°C, more preferably in the range of 1200 to 1450°C, and more preferably in the range of 1225 to 1425°C.

[0053] The reaction in (iv) is preferably carried out by gasification, more preferably by co-flow gasification (German: "Flugstromvergasung").

[0054] In (iv), it is preferable that the mixed feed stream exhibits a holding time in the reaction zone in the range of 1 to 10 seconds.

[0055] The product stream obtained in (iv) preferably contains a mole fraction of CO in the range of 0.30 to 0.95, more preferably in the range of 0.40 to 0.90, and more preferably in the range of 0.45 to 0.88.

[0056] The product stream obtained in (iv) preferably contains a mole fraction of H2 in the range of 0.05 to 0.60, more preferably in the range of 0.10 to 0.50, and more preferably in the range of 0.20 to 0.50.

[0057] This process follows (iv), (v)(iv) Separating CO2 from the product stream obtained in (v)(iv) to obtain a stream containing CO2 and a product stream from which CO2 has been removed. It is preferable to further include the following.

[0058] If the process further includes (v), the separation of CO2 is preferably carried out by a CO2 scrubber or CO2 absorption.

[0059] Furthermore, if this process further includes (v), then this process further includes (v) (vi) The step of compressing the CO2-containing flow obtained in (v) to a flow having a pressure preferably in the range of 5 to 80 bara, preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara. It is preferable that it includes.

[0060] Furthermore, if the process further includes (v), preferably (v) and (vi), according to the first alternative method, the process is performed after (v), preferably after (vi). (vii) The step of recirculating the CO2-containing flow obtained in (v) or (vi) to the first feed flow prepared in (i). It is preferable to further include the following.

[0061] If the process further includes (vii), it is preferable that 1 to 100% by weight, more preferably 25 to 75% by weight, and more preferably 40 to 60% by weight of the CO2 contained in the first feed stream prepared in (i) consists of recirculated CO2 from the CO2-containing stream obtained in (v) or (vi).

[0062] Furthermore, if the process further includes (v), preferably (v) and (vi), according to the second alternative method, the process is performed after (v), preferably after (vi), A step of recirculating the flow containing CO2 obtained in (vii')(v) or (vi) to a first feed flow prepared in (i), wherein the weight ratio of the CO2 recirculated to the first feed flow to the CO2 contained in the first feed flow prepared in (i) is in the range of 1:1 to 5:1, preferably in the range of 1:1 to 2:1, and more preferably in the range of 1:1 to 1.5:1. It is preferable that it includes.

[0063] If the process further includes (vii'), it is preferable that 1 to 100% by weight, more preferably 25 to 75% by weight, and more preferably 40 to 60% by weight of the CO2 recycled into the first feed stream obtained in (vii') consists of CO2 recycled from a CO2-containing stream obtained in (v) or (vi).

[0064] This process is carried out after (iv), preferably after (v), (viii) Adding H2 to the product stream obtained in (iv), or to the product stream from which CO2 has been removed obtained in (v). It is preferable to further include the following.

[0065] If the process further includes (viii), the H2 added to the product stream obtained in (iv) or the product stream from which the CO2 obtained in (v) has been removed preferably includes one or more of the following: H2 obtained from the pipeline, H2 obtained from the tank, H2 obtained from a different process, preferably H2 obtained from a process for preparing styrene, and H2 obtained from electrolysis, preferably electrolysis using green electricity.

[0066] (i) Preparation of the first supply flow is (i.1) A step of preparing a flow containing one or more organic compounds, (i.2) A step of preparing a flow containing CO2, (i.3) The step of mixing the flow containing one or more organic compounds obtained in (i.1) with the flow containing CO2 obtained in (i.2) to obtain a first supply flow. It is preferable that it includes.

[0067] If the step of preparing the first supply flow in (i) includes (i.1), (i.2), and (i.3), the temperature of the flow containing one or more organic compounds prepared in (i.1) is preferably in the range of 10 to 350°C, more preferably in the range of 25 to 300°C, more preferably in the range of 50 to 200°C, and more preferably in the range of 70 to 150°C.

[0068] Furthermore, if the step of preparing the first feed flow in (i) includes (i.1), (i.2), and (i.3), the pressure of the flow containing one or more organic compounds prepared in (i.1) is preferably in the range of 5 to 80 bara, more preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0069] Furthermore, if the step of preparing the first supply flow in (i) includes (i.1), (i.2), and (i.3), the mass flow rate of the flow containing one or more organic compounds prepared in (i.1) is preferably in the range of 100 to 20,000 kg / h, more preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0070] Furthermore, if the step of preparing the first supply flow in (i) includes (i.1), (i.2), and (i.3), the temperature of the CO2-containing flow prepared in (i.2) is preferably in the range of 25 to 380°C, more preferably in the range of 40 to 360°C, and more preferably in the range of 60 to 300°C.

[0071] Furthermore, if the step of preparing the first supply flow in (i) includes (i.1), (i.2), and (i.3), the pressure of the CO2-containing flow prepared in (i.2) is preferably in the range of 5 to 80 bara, more preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0072] Furthermore, if the step of preparing the first supply flow in (i) includes (i.1), (i.2), and (i.3), the mass flow rate of the CO2-containing flow prepared in (i.2) is preferably in the range of 100 to 20,000 kg / h, more preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0073] Furthermore, if the step of preparing the first supply flow in (i) includes (i.1), (i.2), and (i.3), it is preferable that the flow containing CO2 includes one or more of the following: CO2 recirculated from (vii), CO2 recirculated from (vii'), CO2 obtained from different processes for preparing syngas, CO2 obtained from a tank, and CO2 obtained from a pipeline from another plant.

[0074] Preferably, the second feed stream prepared in (ii) contains steam, and the step of preparing the second feed stream in (ii) is: (ii.1) A step of preparing a flow containing O2, (ii.2) A step of preparing a flow containing steam, (ii.3) The step of mixing the flow containing O2 obtained in (ii.1) with the flow containing steam obtained in (ii.2) to obtain a second supply flow. Includes.

[0075] If the second feed stream prepared in (ii) contains steam, and the steps for preparing the second feed stream in (ii) include (ii.1), (ii.2), and (ii.3) as defined herein, the temperature of the O2-containing stream prepared in (ii.1) is preferably in the range of 25 to 400°C, more preferably in the range of 60 to 250°C, and more preferably in the range of 120 to 190°C.

[0076] Furthermore, if the second feed stream prepared in (ii) contains steam, and the steps for preparing the second feed stream in (ii) include (ii.1), (ii.2), and (ii.3) as defined herein, the pressure of the O2-containing stream prepared in (ii.1) is preferably in the range of 5 to 80 bara, more preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0077] Furthermore, if the second feed stream prepared in (ii) contains steam, and the step of preparing the second feed stream in (ii) includes (ii.1), (ii.2), and (ii.3) as defined herein, the mass flow rate of the O2-containing stream prepared in (ii.1) is preferably in the range of 100 to 20,000 kg / h, more preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0078] Furthermore, if the second feed stream prepared in (ii) contains steam, and the step of preparing the second feed stream in (ii) includes (ii.1), (ii.2), and (ii.3) as defined herein, the temperature of the steam-containing stream prepared in (ii.2) is preferably in the range of 200 to 500°C, more preferably in the range of 300 to 450°C, and more preferably in the range of 350 to 425°C.

[0079] Furthermore, if the second feed stream prepared in (ii) contains steam, and the step of preparing the second feed stream in (ii) includes (ii.1), (ii.2), and (ii.3) as defined herein, the pressure of the steam-containing stream prepared in (ii.2) is preferably in the range of 5 to 80 bara, more preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0080] Furthermore, if the second feed stream prepared in (ii) contains steam, and the step of preparing the second feed stream in (ii) includes (ii.1), (ii.2), and (ii.3) as defined herein, the mass flow rate of the steam-containing stream prepared in (ii.2) is preferably less than 6,000 kg / h, more preferably less than 3,000 kg / h, more preferably less than 1,500 kg / h, and more preferably less than 1,000 kg / h.

[0081] The molar ratio of CO2 in the product stream obtained in (iv) to the CO2 in the mixed stream obtained in (iii), CO2 (product stream):CO2 (mixed stream), is preferably less than 1:1.

[0082] The product stream obtained in (iv), or the product stream obtained in (v) from which CO2 has been removed, preferably has a volume ratio of H2 to CO, H2:CO, in the range of 0.1:1 to 1.5:1, more preferably in the range of 0.3:1 to 1.3:1, and more preferably in the range of 0.4:1 to 1.1:1.

[0083] The present invention further preferably relates to a method as described herein, A step of converting a product stream containing H2 and CO, which is available or obtained by the process described herein, or a chemical substance, which is available or obtained by the process described herein, to obtain a monomer, polymer, or polymer product. Regarding methods including

[0084] In preferred embodiments, the monomer is a diol or polyol, preferably butanediol; an aldehyde, preferably formaldehyde; a diisocyanate or polyisocyanate, preferably methylenediphenyl diisocyanate (MDI), polymerizable methylenediphenyl diisocyanate (pMDI), toluene diisocyanate (TDI), hexamethylenediisocyanate (HDI), or isophorone diisocyanate (IPDI); an amide, preferably caprolactam; an alkene, preferably styrene, ethene, and norbornene; an alkyne; a (di)ester, preferably methyl methacrylate; a monoacid or diacid, preferably adipic acid or terephthalic acid; a diamine, preferably hexamethylenediamine, nonanediamine, or sulfone, preferably 4,4'-dichlorodiphenyl sulfone.

[0085] In preferred embodiments, the polymer is polyamide (PA), preferably PA6 or PA66, polyisocyanate polyaddition product, preferably polyurethane (PU), thermoplastic polyurethane (TPU), polyurea or polyisocyanurate (PIR), low-density polyethylene (LDPE), high-density polyethylene (HDPE), polyethylene (PE), polypropylene (PP), polyvinyl chloride (PVC), polyvinyl acetate (PVA), polystyrene (PS), polyacrylonitrile butadiene styrene (ABS), polystyrene acrylonitrile (SAN), polyacrylate styrene acrylonitrile (ASA), polytetrafluoroethylene (PTFE), poly(methyl acrylate) (PMA), poly(methyl methacrylate) (PMMA), polybutadiene (BR, PBD), poly(cis-1,4-isoprene), poly(trans-1,4-isoprene), Polyoxymethylene (POM), poly(ethylene terephthalate) (PET), polybutylene terephthalate (PBT), polybutylene adipate coterephthalate (PBAT), polyester (PES), polyethersulfone (PESU), polyhydroxyalkanoate (PHA), poly-3-hydroxybutyrate (P3HB), poly-4-hydroxybutyrate (P4HB), polyhydroxyvalerate (PHV), polyhydroxyhexanoate (PHH), polyhydroxyoctanoate (PHO), polylactic acid (PLA), polysulfone (PSU), polyphenylene sulfone (PPSU), polycarbonate (PC), polyetheretherketone (PEEK), poly(p-phenylene oxide) (PPO), poly(p-phenylene ether) (PPE), or copolymers or mixtures thereof, and / or polymer products containing these.

[0086] In preferred embodiments, the polymer and / or polymer product is Automotive parts, preferably cylinder head covers, engine covers, housings for charge air coolers, charge air cooler flaps, intake pipes, intake manifolds, connectors, gear wheels, fan wheels, coolant boxes, housings, housing components for heat exchangers, coolant coolers, charge air coolers, thermostats, water pumps, radiators, fastening components, battery system components for electric vehicles, dashboards, steering column switches, seats, headrests, center consoles, transmission components, door modules, A, B, C or D pillar covers, spoilers, door handles, exterior mirrors, windshield wipers, windshield wiper protection housings, decorative grilles, cover strips, roof rails, window frames, sunroof frames, antenna panels, headlights and taillights, engine covers, cylinder head covers, intake manifolds, airbags, cushions, or coatings. Cloth, preferably a shirt, trousers, pullover, boots, shoes, soles, tights or jacket, Electrical components, preferably passive or active electrical or electronic components, circuit boards, printed circuit boards, housing components, foils, lines, switches, plugs, sockets, distributors, relays, resistors, capacitors, inductors, bobbins, lamps, diodes, LEDs, transistors, connectors, regulators, integrated circuits (ICs), processors, controllers, memory, sensors, microswitches, microbuttons, semiconductors, reflector housings for light-emitting diodes (LEDs), fasteners, spacers, bolts, strips, slide-in guides, screws, nuts, film hinges, snap hooks (snap-ins), or spring tongues for electrical or electronic components. Consumer products, agricultural products or pharmaceuticals, preferably tennis strings, climbing ropes, bristle, brushes, artificial turf, 3D printing filaments, grass trimmers, zippers, hook-and-loop fasteners, papermaking equipment, extruded coatings, fishing lines, fishing nets, offshore lines and ropes, vials, syringes, ampoules, bottles, sliding elements, spindle nuts, chain conveyors, sliding bearings, rollers, wheels, gears, rollers, ring gears, screws and spring dampers, hoses, pipelines, cable sheathing, sockets, switches, cable ties, fan wheels, carpets, cosmetic boxes or bottles, mattresses, cushions, insulation materials, detergents, dishwasher tablets or powder detergents, shampoos, body washes, shower gels, soaps, fertilizers, fungicides or insecticides, Packaging for the food industry, preferably single-layer or multi-layer inflation film, cast film (single-layer or multi-layer), biaxially oriented film, or laminate film, Part of a structure, preferably a rotor blade, insulation, frame, housing, wall, coating, or partition wall. It is either or a part of these.

[0087] In preferred embodiments, the content of the feedstock in the product stream, which includes H2 and CO, monomers, polymers, or polymer products, is 1% by weight or more, preferably 2% by weight or more, more preferably 5% by weight or more, more preferably 15% by weight or more, more preferably 30% by weight or more, more preferably 40% by weight or more, more preferably 60% by weight or more, more preferably 80% by weight or more, more preferably 90% by weight or more, more preferably 95% by weight or more, and / or The content of the feedstock in the product stream, which includes H2 and CO, monomers, polymers or polymer products, is 100% by weight or less, preferably 95% by weight or less, more preferably 90% by weight or less, more preferably 50% by weight or less, more preferably 25% by weight or less, and more preferably 10% by weight or less. Preferably, the content is determined based on an identity preservation and / or segregation and / or mass balance and / or book-and-claim management chain model, preferably based on mass balance, and preferably based on International Sustainability Carbon Certification (ISCC) standards.

[0088] In preferred embodiments, the C content derived from the product stream containing H2 and CO contained in the monomer, polymer or polymer product is 1% by weight or more (C is calculated as an element), preferably 2% by weight or more, more preferably 5% by weight or more, more preferably 15% by weight or more, more preferably 30% by weight or more, more preferably 40% by weight or more, more preferably 60% by weight or more, more preferably 80% by weight or more, more preferably 90% by weight or more, more preferably 95% by weight or more, and / or The C content derived from the product flow containing H2 and CO contained in monomers, polymers, or polymer products is 100% by weight or less (C is calculated as an element), preferably 95% by weight or less, more preferably 90% by weight or less, more preferably 50% by weight or less, more preferably 25% by weight or less, and more preferably 10% by weight or less, and Preferably, the content is determined based on an identity preservation and / or segregation and / or mass balance and / or book-and-claim management chain model, preferably based on mass balance, and preferably based on International Sustainability Carbon Certification (ISCC) standards. [Modes for carrying out the invention]

[0089] The present invention is further described by the following series of embodiments and combinations of embodiments arising from the shown dependencies and backreferences. In particular, it should be noted that in each example in which the scope of an embodiment is referred to, for example in the context of the term, for example, “any one process of Embodiments 1 to 4,” all embodiments within this scope are intended to be expressly disclosed to those skilled in the art, i.e., the wording of this term should be understood to those skilled in the art as synonymous with “any one process of Embodiments 1, 2, 3, and 4.” Furthermore, it should be explicitly noted that the following series of embodiments represent a well-structured portion of the general description directed toward preferred aspects of the present invention and therefore adequately support, but do not represent, the claims of the present invention.

[0090] 1. A process for preparing syngas, (i) A step of preparing a first feed stream comprising a liquid phase and a gas phase, wherein the liquid phase comprises one or more organic compounds and the gas phase comprises CO2, (ii) A step of preparing a second feed stream containing O2 and optionally steam, (iii) The step of mixing the first supply flow and the second supply flow to obtain a mixed supply flow, (iv)(iii) The mixed feed stream obtained in (iv)(iii) is reacted in the reaction zone to obtain a product stream containing H2 and CO, and optionally CO2, H2O, or CO2 and H2O. Includes, One or more organic compounds independently contain one or more of C, H, and optionally O, S, and N. process.

[0091] The process according to Embodiment 1, wherein 90 to 100% by weight, preferably 95 to 100% by weight, more preferably 99 to 100% by weight, of one or more organic compounds contained in the liquid phase in the first feed stream prepared in 2.(i) consists of one or more C, H, and optionally O, S, and N.

[0092] 3. The process according to Embodiment 1 or 2, wherein 49.5 to 100% by weight, preferably 60 to 95% by weight, and more preferably 70 to 95% by weight, of 1 or more organic compounds consists of C.

[0093] 4. The process according to any one of Embodiments 1 to 3, wherein 0.5 to 12% by weight, preferably 2 to 11% by weight, and more preferably 4 to 11% by weight of 4 or more organic compounds consist of H.

[0094] 5. The process according to any one of Embodiments 1 to 4, wherein 0 to 50% by weight, preferably 0 to 40% by weight, more preferably 0 to 30% by weight, and more preferably 0 to 20% by weight or less of 5.1 or more organic compounds are present.

[0095] 6. The process according to any one of Embodiments 1 to 5, wherein 0 to 10% by weight, preferably 0 to 6% by weight, and more preferably 0 to 4% by weight of 6.1 or more organic compounds constitute S.

[0096] 7. The process according to any one of Embodiments 1 to 6, wherein 0 to 10% by weight, preferably 0 to 6% by weight, and more preferably 0 to 4% by weight of 7.1 or more organic compounds constitute N.

[0097] 8. The process according to any one of Embodiments 1 to 7, wherein one or more organic compounds contained in the liquid phase are selected from the group consisting of pyrolysis oil, heating oil, vacuum residue, preferably vacuum distillation residue, crude oil residue, heavy crude oil, ultra-heavy crude oil, tar sand bitumen, bisbreaker bottom residue, de-scattering equipment bottom residue, C5 asphaltene fraction, preferably C5 asphaltene, high viscosity residue, bio-oil, fuel oil, pyrolysis gasoline, tire pyrolysis oil (TPO), waste oil, used oil, and mixtures thereof, and the one or more compounds are preferably pyrolysis oil.

[0098] 9. The process according to Embodiment 8, wherein the pyrolysis oil is preferably obtained from the pyrolysis of one or more of biomass, plastic waste, and mixed plastic waste, preferably mixed plastic waste, wherein the mixed plastic waste preferably includes optionally shredded waste tires, and more preferably includes one or more of polyethylene, polypropylene, polyisoprene, polyethylene terephthalate, polystyrene, one or more copolymers thereof, one or more block polymers thereof, one or more graft copolymers thereof, and two or more mixtures thereof.

[0099] 10.The heating oil is (C1-C 100 ) hydrocarbons, preferably (C5-C 80 ) hydrocarbons, more preferably (C 10 -C 60 ) hydrocarbons, more preferably (C 11 -C 40 ) hydrocarbons, more preferably (C 12 -C 25 ) hydrocarbons, more preferably (C 13 -C 21 ) hydrocarbons, preferably (C 14 -C 20 The process according to embodiment 8 or 9, selected from the group consisting of hydrocarbons.

[0100] 11. The process according to any one of Embodiments 8 to 10, wherein the boiling point of the heating oil is preferably in the range of 100 to 1,000°C, preferably in the range of 150 to 750°C, more preferably in the range of 200 to 500°C, more preferably in the range of 225 to 375°C, and more preferably in the range of 250 to 350°C at a pressure in the range of 0.99 to 1.01 bara.

[0101] 12. The process according to any one of Embodiments 1 to 11, wherein the lower heating value of 1 or more organic compounds is in the range of 20 to 60 MJ / kg, preferably in the range of 30 to 50 MJ / kg.

[0102] The process according to any one of Embodiments 1 to 12, wherein 90 to 100% by weight, preferably 95 to 100% by weight, and more preferably 99 to 100% by weight of the gas phase contained in the first feed stream prepared in 13.(i) consists of CO2.

[0103] The process according to any one of Embodiments 1 to 13, wherein the first feed stream prepared in 14.(i) has a weight ratio of one or more organic compounds to CO2, organic compound:CO2, of 1:5 or more, preferably in the range of 1:5 to 1,000:1, more preferably in the range of 1:5 to 500:1, more preferably in the range of 1:5 to 100:1, more preferably in the range of 1:5 to 50:1, more preferably in the range of 1:1 to 25:1, more preferably in the range of 2:1 to 20:1, and more preferably in the range of 5:1 to 15:1.

[0104] The process according to any one of Embodiments 1 to 14, wherein 90 to 100% by weight, preferably 95 to 100% by weight, more preferably 99 to 100% by weight of the first feed stream prepared in 15.(i) consists of one or more organic compounds and CO2.

[0105] The process according to any one of Embodiments 1 to 15, wherein the first feed flow prepared in 16.(i) exhibits a multiphase flow mode, more preferably a two-phase flow mode.

[0106] The process according to any one of Embodiments 1 to 16, wherein the first feed flow prepared in 17.(i) exhibits a dispersed flow pattern, a plug flow pattern, a slug flow pattern, a wave flow pattern, a stratified flow pattern, an annular flow pattern, or a mist flow pattern, preferably a dispersed flow pattern, and the first feed flow prepared in (i) preferably exhibits a horizontal flow pattern.

[0107] The process according to any one of Embodiments 1 to 16, wherein the first feed flow prepared in 18.(i) exhibits a churn flow, annular flow, bubble flow, slug flow, or mist flow, preferably annular flow or mist flow, more preferably mist flow, and the first feed flow prepared in (i) preferably exhibits a vertical flow.

[0108] The process according to any one of Embodiments 1 to 18, wherein the liquid phase of the first feed stream prepared in 19.(i) has a viscosity in the range of 20 to 6,000 mPas, or preferably in the range of 100 to 5,000 mPas, the viscosity of which is preferably determined according to Reference Example 1.

[0109] The process according to any one of Embodiments 1 to 19, wherein the temperature of the first feed stream prepared in 20.(i) is in the range of 50 to 220°C, preferably in the range of 80 to 190°C, and more preferably in the range of 110 to 160°C.

[0110] The process according to any one of Embodiments 1 to 20, wherein the pressure of the first feed stream prepared in 21.(i) is in the range of 5 to 80 bara, preferably in the range of 35 to 60 bara, more preferably in the range of 42 to 52 bara.

[0111] The process according to any one of Embodiments 1 to 21, wherein the mass flow rate of the first feed stream prepared in 22.(i) is in the range of 100 to 20,000 kg / h, preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0112] The process according to any one of Embodiments 1 to 22, wherein 90 to 100% by weight, more preferably 95 to 100% by weight, and more preferably 99 to 100% by weight of the second feed stream prepared in 23.(ii) consists of O2.

[0113] The process according to any one of Embodiments 1 to 23, wherein the second feed stream prepared in 24.(ii) contains steam, and the second feed stream prepared in (ii) preferably has a weight ratio of O2:steam calculated as element O2 to steam calculated as H2O in the range of 1:10 to 100:1, preferably in the range of 1:1 to 61:1.

[0114] The process according to any one of Embodiments 1 to 24, wherein the temperature of the second feed stream prepared in 25.(ii) is in the range of 25 to 400°C, preferably in the range of 50 to 300°C, and more preferably in the range of 90 to 250°C.

[0115] The process according to any one of Embodiments 1 to 25, wherein the pressure of the second feed stream prepared in 26.(ii) is in the range of 5 to 80 bara, preferably in the range of 35 to 60 bara, and more preferably in the range of 40 to 52 bara.

[0116] The process according to any one of Embodiments 1 to 26, wherein the mass flow rate of the second feed stream prepared in 27.(ii) is in the range of 100 to 20,000 kg / h, preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0117] The process according to any one of Embodiments 1 to 27, wherein the mixing step in 28.(iii) is carried out by spraying a first feed stream and a second feed stream to form droplets and optionally liquid fragments of the liquid phase.

[0118] The mixing step in 29.(iii) is (iii.1) Preferably, the first supply flow and the second supply flow are mixed in a mixing chamber to obtain a mixed supply flow, (iii.2) The step of supplying the mixed feed stream obtained in (iii.1) to the reaction zone and The process described in any one of embodiments 1 to 28, including the process described in any one of embodiments 1 to 28.

[0119] The process according to Embodiment 29, wherein the mixing step in 30.(iii.1) is carried out by spraying a mixed feed stream to form droplets and optionally liquid fragments of the liquid phase.

[0120] 31. The process according to Embodiment 29 or 30, wherein the step of supplying a mixed feed stream within the reaction zone is carried out by the step of spraying the mixed feed stream to form droplets and optionally liquid fragments of the liquid phase.

[0121] 32. The spraying step is 100-1500m 3 Range of / h, preferably 200-1000m 3 The process according to embodiment 30 or 31, comprising the step of applying a mixed feed stream with a flow rate in the range of / h.

[0122] The process according to any one of Embodiments 1 to 32, preferably any one of Embodiments 28 to 32, wherein the mixed feed flow obtained in 33.(iii) exhibits a multiphase flow, preferably a two-phase flow.

[0123] The process according to any one of Embodiments 1 to 33, preferably Embodiment 33, wherein the mixed feed flow obtained in 34.(iii) exhibits a dispersed flow mode, a plug flow mode, a slug flow mode, a wave flow mode, a stratified flow mode, an annular flow mode, or a mist flow mode, preferably a dispersed flow mode, and the mixed feed flow obtained in (iii) preferably exhibits a horizontal flow.

[0124] The process according to any one of Embodiments 1 to 33, preferably Embodiment 33, wherein the mixed feed flow obtained in 35(iii) exhibits a churn flow, annular flow, bubble flow, slug flow, or mist flow, preferably annular flow or mist flow, more preferably mist flow, and the mixed feed flow obtained in (iii) preferably exhibits a vertical flow.

[0125] The process according to any one of Embodiments 1 to 35, wherein the weight ratio of one or more organic compounds to O2 in the mixed feed stream obtained in 36.(iii), organic compound:O2, is in the range of 0.10:1 to 2.00:1, preferably 0.25:1 to 1.50:1.

[0126] The process according to any one of Embodiments 1 to 36, wherein the weight ratio of CO2 to O2, CO2:O2, of the mixed feed stream obtained in 37.(iii) is in the range of 1:500 to 1:10, preferably in the range of 1:100 to 1:5.0, more preferably in the range of 1:75 to 1:2.0, and more preferably in the range of 1:50 to 1:1.5.

[0127] The process according to any one of Embodiments 1 to 37, wherein the weight ratio of one or more organic compounds to vapor in the mixed feed stream obtained in 38.(iii) is in the range of 1:1 to 100:1, preferably in the range of 5:1 to 50:1, more preferably in the range of 7:1 to 41:1, and more preferably in the range of 20:1 to 25:1.

[0128] The process according to any one of Embodiments 1 to 38, wherein the reaction in 39.(iv) is carried out at a temperature in the range of 1100 to 1500°C, preferably in the range of 1200 to 1450°C, and more preferably in the range of 1225 to 1425°C.

[0129] The process according to any one of Embodiments 1 to 39, wherein the reaction in 40.(iv) is carried out by gasification, preferably by co-flow gasification (German: "Flugstromvergasung").

[0130] The process according to any one of Embodiments 1 to 40, wherein in 41.(iv), the mixed feed stream exhibits a holding time in the reaction zone in the range of 1 to 10 seconds.

[0131] The process according to any one of Embodiments 1 to 41, wherein the product stream obtained in 42.(iv) contains a mole fraction of CO in the range of 0.30 to 0.95, preferably in the range of 0.40 to 0.90, and more preferably in the range of 0.45 to 0.88.

[0132] The process according to any one of Embodiments 1 to 42, wherein the product stream obtained in 43.(iv) contains a mole fraction of H2 in the range of 0.05 to 0.60, preferably in the range of 0.10 to 0.50, and more preferably in the range of 0.20 to 0.50.

[0133] 44.(iv) followed by (v)(iv) Separating CO2 from the product stream obtained in (v)(iv) to obtain a stream containing CO2 and a product stream from which CO2 has been removed. The process according to any one of embodiments 1 to 43, further including the process described above.

[0134] 45. The process according to Embodiment 44, wherein the separation of CO2 is carried out by a CO2 scrubber or CO2 absorption.

[0135] 46. ​​After (v), (vi) The step of compressing the CO2-containing flow obtained in (v) to a flow having a pressure preferably in the range of 5 to 80 bara, preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara. The process according to embodiment 44 or 45, further comprising:

[0136] 47. After (v), preferably after (vi), (vii) The step of recirculating the CO2-containing flow obtained in (v) or (vi) to the first feed flow prepared in (i). The process according to any one of embodiments 44 to 46, further including the above.

[0137] The process according to Embodiment 47, wherein 1 to 100% by weight, preferably 25 to 75% by weight, and more preferably 40 to 60% by weight of the CO2 contained in the first feed stream prepared in 48.(i) consists of CO2 recycled from the CO2-containing stream obtained in (v) or (vi).

[0138] 49. After (v), preferably after (vi), A step of recirculating the flow containing CO2 obtained in (vii')(v) or (vi) to a first feed flow prepared in (i), wherein the weight ratio of the CO2 recirculated to the first feed flow to the CO2 contained in the first feed flow prepared in (i) is in the range of 1:1 to 5:1, preferably in the range of 1:1 to 2:1, and more preferably in the range of 1:1 to 1.5:1. The process according to any one of embodiments 44 to 46, further including the above.

[0139] The process according to Embodiment 49, wherein 1 to 100% by weight, preferably 25 to 75% by weight, more preferably 40 to 60% by weight of the CO2 recycled to the first feed stream obtained in 50.(vii') consists of CO2 recycled from the CO2-containing stream obtained in (v) or (vi).

[0140] 51. After (iv), preferably after (v), (viii) Add H2 to the product stream obtained in (iv) or the product stream from which CO2 has been removed obtained in (v). The process according to any one of embodiments 1 to 50, further including the process described above.

[0141] The process according to Embodiment 51, wherein the H2 added to the product stream obtained in 52.(iv) or the product stream from which the CO2 obtained in (v) has been removed includes one or more of the following: H2 obtained from a pipeline, H2 obtained from a tank, H2 obtained from a different process, preferably H2 obtained from a process for preparing styrene, and H2 obtained from electrolysis, preferably electrolysis using green electricity.

[0142] The step of preparing the first supply flow in 53.(i) is (i.1) A step of preparing a flow containing one or more organic compounds, (i.2) Step of preparing a flow containing CO2, (i.3) A step of mixing the flow containing one or more organic compounds obtained in (i.1) with the flow containing CO2 obtained in (i.2) to obtain a first feed flow. The process according to any one of embodiments 1 to 52, including the process described above.

[0143] The process according to Embodiment 53, wherein the temperature of the flow containing one or more organic compounds prepared in 54.(i.1) is in the range of 10 to 350°C, preferably in the range of 25 to 300°C, more preferably in the range of 50 to 200°C, and more preferably in the range of 70 to 150°C.

[0144] The process according to Embodiment 53 or 54, wherein the pressure of the flow containing one or more organic compounds prepared in 55.(i.1) is in the range of 5 to 80 bara, preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0145] The process according to any one of Embodiments 53 to 55, wherein the mass flow rate of the flow containing one or more organic compounds prepared in 56.(i.1) is in the range of 100 to 20,000 kg / h, preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0146] The process according to any one of embodiments 53 to 56, wherein the temperature of the flow containing CO2 prepared in 57.(i.2) is in the range of 25 to 380°C, preferably in the range of 40 to 360°C, and more preferably in the range of 60 to 300°C.

[0147] The process according to any one of embodiments 53 to 57, wherein the pressure of the flow containing CO2 prepared in 58.(i.2) is in the range of 5 to 80 bara, preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0148] The process according to any one of Embodiments 53 to 58, wherein the mass flow rate of the CO2-containing flow prepared in 59.(i.2) is in the range of 100 to 20,000 kg / h, preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0149] 60. The process according to any one of embodiments 53 to 59, wherein the flow containing CO2 includes one or more of the following: CO2 recirculated from (vii), CO2 recirculated from (vii'), CO2 obtained from different processes for preparing syngas, CO2 obtained from a tank, and CO2 obtained from a pipeline from another plant.

[0150] The second feed stream prepared in 61.(ii) contains steam, and the step of preparing the second feed stream in (ii) is, (ii.1) A step of preparing a flow containing O2, (ii.2) A step of preparing a flow containing steam, (ii.3) The step of mixing the flow containing O2 obtained in (ii.1) with the flow containing steam obtained in (ii.2) to obtain a second supply flow. A process according to any one of embodiments 1 to 60, including the process described above.

[0151] The process according to Embodiment 61, wherein the temperature of the flow containing O2 prepared in 62.(ii.1) is in the range of 25 to 400°C, preferably in the range of 60 to 250°C, and more preferably in the range of 120 to 190°C.

[0152] The process according to Embodiment 61 or 62, wherein the pressure of the flow containing O2 prepared in 63.(ii.1) is in the range of 5 to 80 bara, preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0153] The process according to any one of embodiments 61 to 63, wherein the mass flow rate of the flow containing O2 prepared in 64.(ii.1) is in the range of 100 to 20,000 kg / h, preferably in the range of 3,000 to 17,000 kg / h, more preferably in the range of 5,000 to 15,000 kg / h, and more preferably in the range of 6,000 to 14,000 kg / h.

[0154] The process according to any one of embodiments 61 to 64, wherein the temperature of the flow containing the steam prepared in 65.(ii.2) is in the range of 200 to 500°C, preferably in the range of 300 to 450°C, and more preferably in the range of 350 to 425°C.

[0155] The process according to any one of embodiments 61 to 65, wherein the pressure of the flow containing the steam prepared in 66.(ii.2) is in the range of 5 to 80 bara, preferably in the range of 35 to 60 bara, and more preferably in the range of 42 to 52 bara.

[0156] The process according to any one of Embodiments 61 to 66, wherein the mass flow rate of the flow containing the steam prepared in 67.(ii.2) is less than 6,000 kg / h, preferably less than 3,000 kg / h, more preferably less than 1,500 kg / h, and more preferably less than 1,000 kg / h.

[0157] The process according to any one of Embodiments 1 to 67, wherein the molar ratio of CO2 in the product stream obtained in 68.(iv) to the CO2 in the mixed stream obtained in (iii), CO2 (product stream):CO2 (mixed stream), is less than 1:1.

[0158] The process according to any one of Embodiments 1 to 68, wherein the product stream obtained in 69.(iv), or the product stream from which CO2 has been removed obtained in (v), has a volume ratio of H2 to CO, H2:CO, in the range of 0.1:1 to 1.5:1, more preferably in the range of 0.3:1 to 1.3:1, and more preferably in the range of 0.4:1 to 1.1:1.

[0159] 70. After (iv), preferably after (v), more preferably after (vi), more preferably after (vii), more preferably after (viii), (ix) A step of converting a product stream containing H2 and CO that is available or obtained by the process described in any one of Embodiments 1 to 69, or a chemical substance that is available or obtained by the process described in any one of Embodiments 1 to 69, to obtain a monomer, polymer, or polymer product. The process described in any one of embodiments 1 to 69, including the process described in any one of embodiments 1 to 69.

[0160] 71. The process according to Embodiment 70, wherein the monomer is a diol or polyol, preferably butanediol; an aldehyde, preferably formaldehyde; a diisocyanate or polyisocyanate, preferably methylenediphenyl diisocyanate (MDI), polymerizable methylenediphenyl diisocyanate (pMDI), toluene diisocyanate (TDI), hexamethylenediisocyanate (HDI), or isophorone diisocyanate (IPDI); an amide, preferably caprolactam; an alkene, preferably styrene, ethene, and norbornene; an alkyne; a (di)ester, preferably methyl methacrylate; a monoacid or diacid, preferably adipic acid or terephthalic acid; a diamine, preferably hexamethylenediamine, nonanediamine, or sulfone, preferably 4,4'-dichlorodiphenylsulfone.

[0161] 72. The polymer is polyamide (PA), preferably PA6 or PA66; polyisocyanate polyaddition product, preferably polyurethane (PU); thermoplastic polyurethane (TPU); polyurea or polyisocyanurate (PIR); low-density polyethylene (LDPE); high-density polyethylene (HDPE); polyethylene (PE); polypropylene (PP); polyvinyl chloride (PVC); polyvinyl acetate (PVA); polystyrene (PS); polyacrylonitrile butadiene styrene (ABS); polystyrene acrylonitrile (SAN); polyacrylate styrene acrylonitrile (ASA); polytetrafluoroethylene (PTFE); poly(methyl acrylate) (PMA); poly(methyl methacrylate) (PMMA); polybutadiene (BR, PBD); poly(cis-1,4-isoprene); poly(trans-1,4-isoprene); polyoxymethylene (POM). The process according to Embodiment 70 or 71, wherein the polymer product is poly(ethylene terephthalate) (PET), polybutylene terephthalate (PBT), polybutylene adipate coterephthalate (PBAT), polyester (PES), polyethersulfone (PESU), polyhydroxyalkanoate (PHA), poly-3-hydroxybutyrate (P3HB), poly-4-hydroxybutyrate (P4HB), polyhydroxyvalerate (PHV), polyhydroxyhexanoate (PHH), polyhydroxyoctanoate (PHO), polylactic acid (PLA), polysulfone (PSU), polyphenylene sulfone (PPSU), polycarbonate (PC), polyetheretherketone (PEEK), poly(p-phenylene oxide) (PPO), poly(p-phenylene ether) (PPE), or copolymers or mixtures thereof, and / or the polymer product contains these.

[0162] 73. Polymers and / or polymer products, Automotive parts, preferably cylinder head covers, engine covers, housings for charge air coolers, charge air cooler flaps, intake pipes, intake manifolds, connectors, gear wheels, fan wheels, coolant boxes, housings, housing components for heat exchangers, coolant coolers, charge air coolers, thermostats, water pumps, radiators, fastening components, battery system components for electric vehicles, dashboards, steering column switches, seats, headrests, center consoles, transmission components, door modules, A, B, C or D pillar covers, spoilers, door handles, exterior mirrors, windshield wipers, windshield wiper protection housings, decorative grilles, cover strips, roof rails, window frames, sunroof frames, antenna panels, headlights and taillights, engine covers, cylinder head covers, intake manifolds, airbags, cushions, or coatings. Cloth, preferably a shirt, trousers, pullover, boots, shoes, soles, tights or jacket, Electrical components, preferably passive or active electrical or electronic components, circuit boards, printed circuit boards, housing components, foils, lines, switches, plugs, sockets, distributors, relays, resistors, capacitors, inductors, bobbins, lamps, diodes, LEDs, transistors, connectors, regulators, integrated circuits (ICs), processors, controllers, memory, sensors, microswitches, microbuttons, semiconductors, reflector housings for light-emitting diodes (LEDs), fasteners, spacers, bolts, strips, slide-in guides, screws, nuts, film hinges, snap hooks (snap-ins), or spring tongues for electrical or electronic components. Consumer products, agricultural products or pharmaceuticals, preferably tennis strings, climbing ropes, bristle, brushes, artificial turf, 3D printing filaments, grass trimmers, zippers, hook-and-loop fasteners, papermaking equipment, extruded coatings, fishing lines, fishing nets, offshore lines and ropes, vials, syringes, ampoules, bottles, sliding elements, spindle nuts, chain conveyors, sliding bearings, rollers, wheels, gears, rollers, ring gears, screws and spring dampers, hoses, pipelines, cable sheathing, sockets, switches, cable ties, fan wheels, carpets, cosmetic boxes or bottles, mattresses, cushions, insulation materials, detergents, dishwasher tablets or powder detergents, shampoos, body washes, shower gels, soaps, fertilizers, fungicides or insecticides, Packaging for the food industry, preferably single-layer or multi-layer inflation film, cast film (single-layer or multi-layer), biaxially oriented film, or laminate film, Part of a structure, preferably a rotor blade, insulation, frame, housing, wall, coating, or partition wall. The process described in any one of embodiments 70 to 72, which is either or a part thereof.

[0163] 74. The content of the feed material in the product stream, which includes H2 and CO, monomers, polymers or polymer products, is 1% by weight or more, preferably 2% by weight or more, more preferably 5% by weight or more, more preferably 15% by weight or more, more preferably 30% by weight or more, more preferably 40% by weight or more, more preferably 60% by weight or more, more preferably 80% by weight or more, more preferably 90% by weight or more, more preferably 95% by weight or more, and / or The content of the feedstock in the product stream, which includes H2 and CO, monomers, polymers or polymer products, is 100% by weight or less, preferably 95% by weight or less, more preferably 90% by weight or less, more preferably 50% by weight or less, more preferably 25% by weight or less, and more preferably 10% by weight or less, and Preferably, the content is determined based on an identity preservation and / or segregation and / or mass balance and / or book embodiment management chain model, preferably based on mass balance, and preferably based on International Sustainability Carbon Certification (ISCC) standards, according to any one of embodiments 70 to 73.

[0164] 75. The C content derived from the product stream containing H2 and CO contained in the monomer, polymer or polymer product is 1% by weight or more (C is calculated as an element), preferably 2% by weight or more, more preferably 5% by weight or more, more preferably 15% by weight or more, more preferably 30% by weight or more, more preferably 40% by weight or more, more preferably 60% by weight or more, more preferably 80% by weight or more, more preferably 90% by weight or more, more preferably 95% by weight or more, and / or The C content derived from the product flow containing H2 and CO contained in monomers, polymers, or polymer products is 100% by weight or less (C is calculated as an element), preferably 95% by weight or less, more preferably 90% by weight or less, more preferably 50% by weight or less, more preferably 25% by weight or less, and more preferably 10% by weight or less, and Preferably, the content is determined based on an identity preservation and / or segregation and / or mass balance and / or book and claim management chain model, preferably based on mass balance, and preferably based on International Sustainability Carbon Certification (ISCC) standards. The process described in any one of embodiments 70 to 73.

[0165] The unit bara is an absolute pressure of 10⁻⁶ 5 This refers to Pa.

[0166] The present invention is further illustrated by the following embodiments.

[0167] Examples Reference Example 1: Measurement of liquid phase viscosity Viscosity was measured at 20°C using a Brookfield RV type laboratory viscometer with a spindle #4 or #5 at 100 revolutions per minute, in accordance with the standard method DIN EN ISO 3219:1994.

[0168] Comparative Example 0 and Examples 1-5: Process for preparing syngas The process for preparing the syngas was simulated using Aspen (Aspen version V14). To prepare the first feed stream according to the present invention, a feed stream containing an organic compound was mixed with a CO2-containing feed stream.

[0169] The conditions described in Tables 1-3 below were set. The pressures of the high-pressure-reduced residue flow, CO2 flow, steam flow for the first feed flow, O2 flow, steam flow for the second feed flow, the first feed flow, and the second feed flow were set independently to 47 bara.

[0170] The prepared flows were mixed and reacted by gasification.

[0171] [Table 1]

[0172] [Table 2]

[0173] [Table 3]

[0174] [Table 4]

[0175] In Examples 15 and 16, the weight ratios of organic matter to CO2 in the first feed stream were 47 and 0.22, respectively.

[0176] In Comparative Example 17, the weight ratio of organic matter to CO2 in the first feed stream was 0.18. Due to the CO2, a flame could not develop, and the gasification reaction did not occur. Therefore, the required temperature in the reactor was not reached, and the simulation could not be performed. Consequently, no results were obtained for Comparative Example 17.

[0177] As can be inferred from the results, a process for preparing syngas can be provided that reduces the amount of steam. Furthermore, the process according to the present invention allows for the recirculation of CO2. In particular, the recirculated CO2 can be used to spray the liquid feed stream. Thus, syngas with a relatively high CO content can be prepared according to the present invention. In addition, it has been found that by recirculating CO2, mass flow rate leveling is achieved, and as a result, a steady-state process can be realized.

[0178] References International Publication No. 2015 / 090575(A1) Pamphlet International Publication No. 2022 / 200532(A1) Brochure U.S. Patent No. 10435295 U.S. Patent Application Publication No. 2016 / 0362355(A1) International Publication No. 2021 / 180482(A1) brochure U.S. Patent Application Publication No. 2022 / 234889(A1) European Patent Application Publication No. 3878807

Claims

1. A process for preparing syngas, wherein the method is (i) A step of preparing a first feed stream comprising a liquid phase and a gas phase, wherein the liquid phase comprises one or more organic compounds and the gas phase is CO 2 The first feed stream prepared in (i) contains the one or more organic compounds and CO 2 Weight ratio of organic compounds: CO 2 The step is 1:5 or more, (ii) O 2 The steps include preparing a second supply stream which may include steam, (iii) The step of mixing the first supply flow and the second supply flow to obtain a mixed supply flow, (iv) reacting the mixed feed stream obtained in (iii) in a reaction zone to obtain H 2 and CO, optionally containing CO 2 , H 2 O or CO 2 and H 2 obtaining a product stream comprising O Includes, The one or more organic compounds described above independently contain C, H, and optionally one or more of O, S, and N. process.

2. The process according to claim 1, wherein the one or more organic compounds contained in the liquid phase are selected from the group consisting of pyrolysis oil, heating oil, vacuum residue, crude oil residue, heavy crude oil, ultra-heavy crude oil, tar sand bitumen, bisbreaker bottom residue, de-scraper bottom residue, C5 asphaltene fraction, high viscosity residue, bio-oil, fuel oil, pyrolysis gasoline, tire pyrolysis oil (TPO), waste oil, used oil, and mixtures thereof.

3. (i) The one or more organic compounds and CO 2 Weight ratio of organic compounds: CO 2 The process according to claim 1 or 2, wherein the ratio is in the range of 1:5 to 1,000:

1.

4. The process according to any one of claims 1 to 3, wherein the temperature of the first feed stream prepared in (i) is in the range of 50 to 220°C.

5. The process according to any one of claims 1 to 4, wherein the pressure of the first supply flow prepared in (i) is in the range of 5 to 80 bara.

6. The process according to any one of claims 1 to 5, wherein the temperature of the second supply stream prepared in (ii) is in the range of 25 to 400°C.

7. The process according to any one of claims 1 to 6, wherein the pressure of the second supply flow prepared in (ii) is in the range of 5 to 80 bara.

8. The process according to any one of claims 1 to 7, wherein the mixing step in (iii) is carried out by spraying the first and second supply streams to form droplets and optionally liquid fragments of the liquid phase.

9. (iii) The mixed feed stream obtained in the above-mentioned one or more organic compounds and O 2 Weight ratio of organic compounds: O 2 The process according to any one of claims 1 to 8, wherein the ratio is in the range of 0.10:1 to 2.00:

1.

10. The CO of the mixed feed stream obtained in (iii) 2 and O 2 CO2 by weight 2 : O 2 The process according to any one of claims 1 to 9, wherein the ratio is in the range of 1:500 to 1:

10.

11. The process according to any one of claims 1 to 10, wherein the reaction in (iv) is carried out at a temperature in the range of 1100 to 1500°C.

12. The process according to any one of claims 1 to 11, wherein the reaction in (iv) is carried out by gasification.

13. (iv) followed by, From the product stream obtained in (v)(iv), CO 2 Separate CO 2 Flows including CO 2 Steps to obtain a product stream from which the product has been removed. The process according to any one of claims 1 to 12, further comprising:

14. (v) followed by, CO obtained in (vi)(v) 2 A step of compressing the flow including The process according to claim 13, further comprising:

15. (v) followed by, CO obtained in (vii)(v) or (vi) 2 (i) A step of recirculating the flow including into the first supply flow prepared in (i) The process according to claim 13 or 14, further comprising:

16. (iv) followed by, (ix) H which is available or obtained by the process described in any one of claims 1 to 15 2 A step of converting the product stream containing CO, or a chemical substance available or obtained by the process described in any one of claims 1 to 15, to obtain a monomer, polymer, or polymer product. The process according to any one of claims 1 to 15, including the process described in any one of claims 1 to 15.

17. The process according to claim 16, wherein the monomer is a diol or polyol, an aldehyde, a diisocyanate or polyisocyanate, polymerizable methylenediphenyl diisocyanate (pMDI), toluene diisocyanate (TDI), hexamethylene diisocyanate (HDI) or isophorone diisocyanate (IPDI), an amide, an alkene, an ethene and norbornene, an alkyne, a (di)ester, a monoacid or diacid, a diamine, a nonanediamine, or a sulfone.

18. The polymers mentioned above include polyamide (PA), polyisocyanate polyaddition products, thermoplastic polyurethane (TPU), polyurea or polyisocyanurate (PIR), low-density polyethylene (LDPE), high-density polyethylene (HDPE), polyethylene (PE), polypropylene (PP), polyvinyl chloride (PVC), polyvinyl acetate (PVA), polystyrene (PS), polyacrylonitrile butadiene styrene (ABS), polystyrene acrylonitrile (SAN), polyacrylate styrene acrylonitrile (ASA), polytetrafluoroethylene (PTFE), poly(methyl acrylate) (PMA), poly(methyl methacrylate) (PMMA), polybutadiene (BR, PBD), poly(cis-1,4-isoprene), poly(trans-1,4-isoprene), polyoxymethylene (POM), and polyethylene tetrafluoroethylene. Rephthalate (PET), polybutylene terephthalate (PBT), polybutylene adipate coterephthalate (PBAT), polyester (PES), polyethersulfone (PESU), polyhydroxyalkanoate (PHA), poly-3-hydroxybutyrate (P3HB), poly-4-hydroxybutyrate (P4HB), polyhydroxyvalerate (PHV), polyhydroxyhexanoate (PHH), polyhydroxyoctanoate (PHO), polylactic acid (PLA), polysulfone (PSU), polyphenylene sulfone (PPSU), polycarbonate (PC), polyetheretherketone (PEEK), poly(p-phenylene oxide) (PPO), poly(p-phenylene ether) (PPE), and copolymers and mixtures thereof, and / or polymer products containing these, The process according to claim 16 or 17.

19. The polymer and / or the polymer product Automotive parts, engine covers, charge air cooler housings, charge air cooler flaps, intake pipes, intake manifolds, connectors, gear wheels, fan wheels, coolant boxes, housings, housing components for heat exchangers, coolant coolers, charge air coolers, thermostats, water pumps, radiators, fasteners, battery system components for electric vehicles, dashboards, steering column switches, seats, headrests, center consoles, transmission components, door modules, A, B, C or D pillar covers, spoilers, door handles, exterior mirrors, windshield wipers, windshield wiper protection housings, decorative grilles, cover strips, roof rails, window frames, sunroof frames, antenna panels, headlights and taillights, engine covers, cylinder head covers, intake manifolds, airbags, cushions, or coatings. Cloth, trousers, pullover, boots, shoes, soles, tights or jacket, Electrical components, circuit boards, printed circuit boards, housing components, foil, lines, switches, plugs, sockets, distributors, relays, resistors, capacitors, inductors, bobbins, lamps, diodes, LEDs, transistors, connectors, regulators, integrated circuits (ICs), processors, controllers, memory, sensors, microswitches, microbuttons, semiconductors, reflector housings for light-emitting diodes (LEDs), fasteners, spacers, bolts, strips, slide-in guides, screws, nuts, film hinges, snap hooks (snap-ins), or spring tongues for electrical or electronic components. Consumer products, agricultural products or pharmaceuticals, climbing ropes, bristle, brushes, artificial turf, 3D printing filaments, grass trimmers, zippers, hook-and-loop fasteners, papermaking equipment, extruded coatings, fishing lines, fishing nets, offshore lines and ropes, vials, syringes, ampoules, bottles, sliding elements, spindle nuts, chain conveyors, plain bearings, rollers, wheels, gears, rollers, ring gears, screws and spring dampers, hoses, pipelines, cable sheathing, sockets, switches, cable ties, fan wheels, carpets, cosmetic boxes or bottles, mattresses, cushions, insulation, detergents, dishwasher tablets or powder detergents, shampoos, body washes, shower gels, soaps, fertilizers, fungicides or insecticides, and / or - Packaging for the food industry, cast film (single or multilayer), biaxially oriented film, or laminate film, Part of a structure, insulation, frame, housing, wall, coating, or partition wall The process according to any one of claims 16 to 18, which is either or a part thereof.

20. H contained in the monomer, polymer or polymer product 2 The content of C derived from the product stream containing CO is 1% by weight or more, and / or H contained in the monomer, polymer or polymer product 2 and the content of C derived from the product stream containing CO is 100% by weight or less. The process according to any one of claims 16 to 19.

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