[go: up one dir, main page]

WO2018096018A1 - Multi bed reactor comprising an adiabatic and a heated catalyst bed - Google Patents

Multi bed reactor comprising an adiabatic and a heated catalyst bed Download PDF

Info

Publication number
WO2018096018A1
WO2018096018A1 PCT/EP2017/080157 EP2017080157W WO2018096018A1 WO 2018096018 A1 WO2018096018 A1 WO 2018096018A1 EP 2017080157 W EP2017080157 W EP 2017080157W WO 2018096018 A1 WO2018096018 A1 WO 2018096018A1
Authority
WO
WIPO (PCT)
Prior art keywords
catalyst
reactor
adiabatic
catalyst bed
heated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2017/080157
Other languages
French (fr)
Inventor
Per Juul Dahl
Helbo Anders HANSEN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Topsoe AS
Original Assignee
Haldor Topsoe AS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Haldor Topsoe AS filed Critical Haldor Topsoe AS
Publication of WO2018096018A1 publication Critical patent/WO2018096018A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/04Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/04Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds
    • B01J8/0446Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/04Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds
    • B01J8/0446Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical
    • B01J8/0449Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical in two or more cylindrical beds
    • B01J8/0453Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical in two or more cylindrical beds the beds being superimposed one above the other
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/04Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds
    • B01J8/0446Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical
    • B01J8/0461Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds the flow within the beds being predominantly vertical in two or more cylindrical annular shaped beds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/06Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds in tube reactors; the solid particles being arranged in tubes
    • B01J8/067Heating or cooling the reactor
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/384Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts the catalyst being continuously externally heated
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00522Controlling the temperature using inert heat absorbing solids outside the bed
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00743Feeding or discharging of solids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00796Details of the reactor or of the particulate material
    • B01J2208/00805Details of the particulate material
    • B01J2208/00814Details of the particulate material the particulate material being provides in prefilled containers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00796Details of the reactor or of the particulate material
    • B01J2208/00884Means for supporting the bed of particles, e.g. grids, bars, perforated plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/02Processes carried out in the presence of solid particles; Reactors therefor with stationary particles
    • B01J2208/023Details
    • B01J2208/024Particulate material
    • B01J2208/025Two or more types of catalyst
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00002Chemical plants
    • B01J2219/00018Construction aspects
    • B01J2219/00024Revamping, retrofitting or modernisation of existing plants
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/04Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds
    • B01J8/0496Heating or cooling the reactor
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/0205Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0227Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
    • C01B2203/0233Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a steam reforming step

Definitions

  • Multi bed reactor comprising an adiabatic and a heated catalyst bed
  • prereforming reactors During the last 25 years use of separate prereforming reactors has become common part of the steam reforming section in synthesis gas preparation plants. In the begin- ning this was driven by the need to reform feed stocks with content of higher hydrocarbons.
  • Today prereforming is also used to reduce the size of the downstream primary reformer and to protect the catalyst in the primary reformer even in case of feedstocks with low content of hydrocarbon.
  • a prereforming step is an excellent catalyst guard removing for example all Sulphur components quantitatively.
  • the prereforming - primary reforming concept is a well-established concept in the industry
  • Prereforming protects the primary reforming catalyst typically increasing the expected lifetime from 3-5 to 10 years. Over a 10 years' period 1 to 2 primary reformer catalyst exchanges are thus avoided. As it is time consuming to change primary reformer catalyst this is a huge economic benefit, more than covering the cost of having a prereform- ing step.
  • Heat exchange reformers where a hot gas stream is used as heat source for the reforming process through heat exchange, are typical very compacts designs where catalyst is even more difficult to change than in a primary reformer. It is therefore very rel- evant to have a prereforming step before a heat exchange reformer. Heat exchange reformers are often used for revamps to increase the reforming capacity. This is also feasible for ammonia plants, which typically have no prereforming step and where it typically will not be economically feasible to install a separate prereforming step. In a first aspect of the present invention is provided a reactor which provides reduced equipment/piping cost.
  • a reactor which provides reduced plot space requirement thereby enabling cost savings and increased versatility of the reactor.
  • a rector comprising a guard layer and/or adiabatic catalyst layer and a heated catalyst bed.
  • a single reactor comprising a heated catalyst bed as well as a guard layer and/or adiabatic catalyst layer is provided whereby significant CAPEX savings may be achieved compared to known multi reactor setups.
  • the present invention thus combines prereforming and heat exchange reforming in a single reactor with no or minimal impact on the reactor dimensions.
  • the added cost of having a prereforming step protecting the heat exchange reforming step is therefore merely the catalyst cost making the combined solution economically feasible against a solution with no prereforming step, considering the heat exchange reformer catalyst exchange cost.
  • the heated catalyst bed is downstream the guard layer and/or adiabatic catalyst layer.
  • the outlet from the guard layer and/or adiabatic catalyst layer is the inlet to the heated catalyst bed. This way the reaction gas which enters the reactor first passes the guard layer and/or adiabatic catalyst layer and thereafter the heated catalyst bed.
  • the reaction gas first passes the guard layer and/or adiabatic catalyst layer i.e. when the adiabatic catalyst layer is arranged upstream the heated catalyst bed the lifetime of the catalyst in the heated catalyst bed may be significantly increased.
  • the heated catalyst bed is an exchange reformer, the process of changing the catalyst in the heated cata- lyst bed is relatively demanding in which case it may be highly desirable to be able to enhance the life time of the heated catalyst by adding the guard layer and/or adiabatic catalyst layer which furthermore may be simpler/faster/easier to change.
  • the guard layer and/or adiabatic catalyst layer may e.g. be a Sulphur guard, a hydro- carbon desulphurisation catalyst and/or a hydrocarbon steam reforming catalyst.
  • the catalyst in the heated catalyst bed may preferably be a hydrocarbon steam reforming catalyst.
  • the present reactor may be specifically designed and provided from new to comprise the heated catalyst bed as well as the guard layer and/or adiabatic catalyst layer.
  • the present reactor may alternatively be provided as a revamp solution to existing reactors comprising one or more heated catalyst beds.
  • the present reactor may be provided as a revamp to existing exchange reformers.
  • a heated catalyst bed is present in the reactor.
  • Above the heated catalyst bed is a hollow in known setups due to gas distribution requirements. The applicant has shown that this free space above the heated catalyst bed in a revamp solution advantageously may used for a guard layer and/or adiabatic catalyst layer.
  • the inventions is not limited to the prereforming - primary reformer concept but can also be used for other processes where a combination of an adiabatic/guard reactor and a heat exchange reactor is used.
  • An example of this could be a steam fired reverse shift reactor in combination with a chlorine/Sulphur guard layer.
  • the invention is valid for process combinations where the first step is the heat exchange reactor and the second step a guard/catalyst layer.
  • the heat exchange reactor has inherently also an empty room in the outlet head providing room for a guard/catalyst layer.
  • the guard/catalyst layer can for example be used to remove/convert bi-products formed in the heat exchange reactor step
  • Table 1 shows a typical set of process conditions for a heat exchange reformer.
  • the REACTOR INLET stream is send through a number of reforming catalyst containing tubes. These tubes are heated from outside by cooling the HEAT SOURCE gas. Before leaving the reactor the outlet gas from the catalyst containing tubes is mixed with the cooled heat source gas to form the final PRODUCT gas.
  • Table 2 shows the effect of sending the INLET REACTOR gas through an adiabatic pre-reforming catalyst layer before it is send through the heated reforming catalyst con- taining tubes.
  • the INTERMEDIATE shows the outlet stream from the adiabatic pre-reforming catalyst layer. It is seen that no higher hydrocarbons are present in this stream. Furthermore, Sulphur components in the INLET REACTOR stream will be absorbed by the pre reforming catalyst. These two effects increase the lifetime of the reforming catalyst in the tubes from approximate 3 years to 10 years. As a secondary effect the ca- pacity can be increased.
  • Figure 1 b) - f) show various examples of how a guard/adiabatic catalyst layer (1 ) can be integrated in a heat exchange reformer (2) with no or minimum change of the reactor dimensions.
  • the adiabatic catalyst layer (1 ) is placed in the entrance head of the heat exchange reformer (2), where there typically is an empty room, such that the incoming gas is send through this adiabatic catalyst layer 1 before entering the catalyst tubes (3).
  • Figure 1 b) provides example of a simple solution placing the guard/catalyst layer directly on the top of the tube sheet only separated by a grid (4) preventing catalyst from falling into the tubes.
  • Figure 1 c) - f) provides various examples of one or more cassette's (5) which easily can be taken in and out of the reactor for quick catalyst exchange.
  • Figure 1 shows a standard heat exchange reformer without an adiabatic catalyst layer.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Inorganic Chemistry (AREA)
  • Hydrogen, Water And Hydrids (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)

Abstract

The present application relates to a reactor comprising a heated catalyst bed and a guard layer and/or adiabatic catalyst, as well as a method for revamping an existing actor having at least a heated catalyst bed.

Description

Title: Multi bed reactor comprising an adiabatic and a heated catalyst bed
During the last 25 years use of separate prereforming reactors has become common part of the steam reforming section in synthesis gas preparation plants. In the begin- ning this was driven by the need to reform feed stocks with content of higher hydrocarbons. Today prereforming is also used to reduce the size of the downstream primary reformer and to protect the catalyst in the primary reformer even in case of feedstocks with low content of hydrocarbon. A prereforming step is an excellent catalyst guard removing for example all Sulphur components quantitatively. The prereforming - primary reforming concept is a well-established concept in the industry
There is still a reluctance to use prereforming in the ammonia industry. Partly because of conservatism, partly because of process integration problems as a prereforming step may reduce required steam production.
Prereforming protects the primary reforming catalyst typically increasing the expected lifetime from 3-5 to 10 years. Over a 10 years' period 1 to 2 primary reformer catalyst exchanges are thus avoided. As it is time consuming to change primary reformer catalyst this is a huge economic benefit, more than covering the cost of having a prereform- ing step.
Heat exchange reformers, where a hot gas stream is used as heat source for the reforming process through heat exchange, are typical very compacts designs where catalyst is even more difficult to change than in a primary reformer. It is therefore very rel- evant to have a prereforming step before a heat exchange reformer. Heat exchange reformers are often used for revamps to increase the reforming capacity. This is also feasible for ammonia plants, which typically have no prereforming step and where it typically will not be economically feasible to install a separate prereforming step. In a first aspect of the present invention is provided a reactor which provides reduced equipment/piping cost.
In a first aspect of the present invention is provided a reactor which provides reduced plot space requirement thereby enabling cost savings and increased versatility of the reactor.
These and other advantages are achieved by a rector comprising a guard layer and/or adiabatic catalyst layer and a heated catalyst bed. I.e. by the present invention a single reactor comprising a heated catalyst bed as well as a guard layer and/or adiabatic catalyst layer is provided whereby significant CAPEX savings may be achieved compared to known multi reactor setups.
The present invention thus combines prereforming and heat exchange reforming in a single reactor with no or minimal impact on the reactor dimensions. The added cost of having a prereforming step protecting the heat exchange reforming step is therefore merely the catalyst cost making the combined solution economically feasible against a solution with no prereforming step, considering the heat exchange reformer catalyst exchange cost.
Combining a guard/catalyst layer and a heat exchange reactor step in one reactor provides:
Reduced equipment/piping cost
- Reduced plot space requirement saving cost and increased possibility to installed the solution as part of a revamp of an existing plant.
Possibility for easy exchange of guard/catalyst layer without affecting the heat exchange catalyst. Preferably the heated catalyst bed is downstream the guard layer and/or adiabatic catalyst layer. I.e. preferably the outlet from the guard layer and/or adiabatic catalyst layer is the inlet to the heated catalyst bed. This way the reaction gas which enters the reactor first passes the guard layer and/or adiabatic catalyst layer and thereafter the heated catalyst bed.
When the reaction gas first passes the guard layer and/or adiabatic catalyst layer i.e. when the adiabatic catalyst layer is arranged upstream the heated catalyst bed the lifetime of the catalyst in the heated catalyst bed may be significantly increased. Having the guard layer and/or adiabatic catalyst layer separate from the heated catalyst bed it is possible to change the guard layer and/or adiabatic catalyst more frequently than the catalyst in the heated catalyst layer. If for example the heated catalyst bed is an exchange reformer, the process of changing the catalyst in the heated cata- lyst bed is relatively demanding in which case it may be highly desirable to be able to enhance the life time of the heated catalyst by adding the guard layer and/or adiabatic catalyst layer which furthermore may be simpler/faster/easier to change.
The guard layer and/or adiabatic catalyst layer may e.g. be a Sulphur guard, a hydro- carbon desulphurisation catalyst and/or a hydrocarbon steam reforming catalyst.
The catalyst in the heated catalyst bed may preferably be a hydrocarbon steam reforming catalyst. The present reactor may be specifically designed and provided from new to comprise the heated catalyst bed as well as the guard layer and/or adiabatic catalyst layer.
However, the present reactor may alternatively be provided as a revamp solution to existing reactors comprising one or more heated catalyst beds. For example the present reactor may be provided as a revamp to existing exchange reformers.
In existing reactors, such as exchange reformers, a heated catalyst bed is present in the reactor. Above the heated catalyst bed is a hollow in known setups due to gas distribution requirements. The applicant has shown that this free space above the heated catalyst bed in a revamp solution advantageously may used for a guard layer and/or adiabatic catalyst layer.
The inventions is not limited to the prereforming - primary reformer concept but can also be used for other processes where a combination of an adiabatic/guard reactor and a heat exchange reactor is used. An example of this could be a steam fired reverse shift reactor in combination with a chlorine/Sulphur guard layer. Similarly, the invention is valid for process combinations where the first step is the heat exchange reactor and the second step a guard/catalyst layer. The heat exchange reactor has inherently also an empty room in the outlet head providing room for a guard/catalyst layer. The guard/catalyst layer can for example be used to remove/convert bi-products formed in the heat exchange reactor step
Table 1 shows a typical set of process conditions for a heat exchange reformer. The REACTOR INLET stream is send through a number of reforming catalyst containing tubes. These tubes are heated from outside by cooling the HEAT SOURCE gas. Before leaving the reactor the outlet gas from the catalyst containing tubes is mixed with the cooled heat source gas to form the final PRODUCT gas.
Table 1
INLET HEAT
STREAM DESCRIPTION REACTOR SOURCE PRODUCT
FLOW (nm3/h) 31631,40 263331,60 308659,20
TEMP (°C) 359,88 1010,52 798,95
PRESSURE (bar g) 30,94 30,94 30,32
COMPOSITION (dry mole%)
Hydrogen 3,75 51,31 54,67
Nitrogen 1,51 27,45 23,56
Carbon Monoxide 0,00 13,31 13,73
Carbon Dioxide 2,12 7,45 7,48
Argon 0,02 0,33 0,28
Methane 84,23 0,14 0,29
Ethane 4,47 0,00 0,00
Propane 2,53 0,00 0,00 n-Butane 0,48 0,00 0,00 n-Pentane 0,09 0,00 0,00 n-Hexane 0,08 0,00 0,00
Isobutane 0,55 0,00 0,00
2-Methylbutane 0,16 0,00 0,00
Table 1: Heat exchange reformer without
adiabatic prereformer bed Table 2
Figure imgf000006_0001
Table 2 shows the effect of sending the INLET REACTOR gas through an adiabatic pre-reforming catalyst layer before it is send through the heated reforming catalyst con- taining tubes. The INTERMEDIATE shows the outlet stream from the adiabatic pre-reforming catalyst layer. It is seen that no higher hydrocarbons are present in this stream. Furthermore, Sulphur components in the INLET REACTOR stream will be absorbed by the pre reforming catalyst. These two effects increase the lifetime of the reforming catalyst in the tubes from approximate 3 years to 10 years. As a secondary effect the ca- pacity can be increased.
Figure 1 b) - f) show various examples of how a guard/adiabatic catalyst layer (1 ) can be integrated in a heat exchange reformer (2) with no or minimum change of the reactor dimensions. The adiabatic catalyst layer (1 ) is placed in the entrance head of the heat exchange reformer (2), where there typically is an empty room, such that the incoming gas is send through this adiabatic catalyst layer 1 before entering the catalyst tubes (3). Figure 1 b) provides example of a simple solution placing the guard/catalyst layer directly on the top of the tube sheet only separated by a grid (4) preventing catalyst from falling into the tubes. Figure 1 c) - f) provides various examples of one or more cassette's (5) which easily can be taken in and out of the reactor for quick catalyst exchange. Solutions are not limited to what is shown in Figure 1 . The principle can also be adopted in heat exchange reformer designs with different entrance head design and dimensions. Typically, there will inherently be an empty entrance room used for gas distribution which is large enough to install a feasible guard/catalyst layer. Figure 1 a) shows a standard heat exchange reformer without an adiabatic catalyst layer.

Claims

Claims
1 . A reactor comprising an adiabatic catalyst bed and a heated catalyst bed.
2. A reactor according to claim 1 wherein the product gas leaving the adiabatic catalyst bed is inlet gas to the heated catalyst bed.
3. A reactor according to claim 1 and 2 wherein the adiabatic catalyst bed comprises a hydrocarbon steam reforming catalyst.
4. A reactor according to claim 1 and 2 wherein the adiabatic catalyst bed comprises a hydrocarbon desulphurisation catalyst.
5. A reactor according to claim 1 and 2 wherein the heated catalyst bed comprises a hydrocarbon steam reforming catalyst.
6. A reactor according to any of the preceding claims wherein said reactor is a heat exchange reformer.
7. A hydrocarbon steam reforming process using the reactor according to any of the claims 1 - 6.
8. A method for revamping an existing reactor having at least a heated catalyst bed, said method comprising
- providing a guard layer and/or adiabatic catalyst layer in said existing reactor.
9. A method according to claim 8 wherein the product gas wherein the heated catalyst bed is downstream the adiabatic catalyst bed.
10. A method according to claim 8 or 9 wherein the adiabatic catalyst bed is filled with hydrocarbon steam reforming catalyst.
PCT/EP2017/080157 2016-11-24 2017-11-23 Multi bed reactor comprising an adiabatic and a heated catalyst bed Ceased WO2018096018A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DKPA201600727 2016-11-24
DKPA201600727 2016-11-24

Publications (1)

Publication Number Publication Date
WO2018096018A1 true WO2018096018A1 (en) 2018-05-31

Family

ID=60629660

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2017/080157 Ceased WO2018096018A1 (en) 2016-11-24 2017-11-23 Multi bed reactor comprising an adiabatic and a heated catalyst bed

Country Status (1)

Country Link
WO (1) WO2018096018A1 (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5464606A (en) * 1994-05-27 1995-11-07 Ballard Power Systems Inc. Two-stage water gas shift conversion method
US5928614A (en) * 1996-06-19 1999-07-27 Daimler Benz Ag Reforming reactor, particularly for the water vapor reforming of methanol
CN2621805Y (en) * 2003-06-03 2004-06-30 华东理工大学 Shell external cooling-thermal insulating and combined fixed bed catalyst chember
WO2007000244A1 (en) * 2005-06-28 2007-01-04 Haldor Topsøe A/S Compact reforming reactor
CN102649564A (en) * 2011-02-25 2012-08-29 中国石油化工股份有限公司 Method for dehydrogenating CO-containing mixed gas raw material by means of catalytic oxidation reaction
CN105536654A (en) * 2015-12-15 2016-05-04 惠生工程(中国)有限公司 Large-scale axial multistage-mixing heat exchange type oxydehydrogenation reactor for butylene

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5464606A (en) * 1994-05-27 1995-11-07 Ballard Power Systems Inc. Two-stage water gas shift conversion method
US5928614A (en) * 1996-06-19 1999-07-27 Daimler Benz Ag Reforming reactor, particularly for the water vapor reforming of methanol
CN2621805Y (en) * 2003-06-03 2004-06-30 华东理工大学 Shell external cooling-thermal insulating and combined fixed bed catalyst chember
WO2007000244A1 (en) * 2005-06-28 2007-01-04 Haldor Topsøe A/S Compact reforming reactor
CN102649564A (en) * 2011-02-25 2012-08-29 中国石油化工股份有限公司 Method for dehydrogenating CO-containing mixed gas raw material by means of catalytic oxidation reaction
CN105536654A (en) * 2015-12-15 2016-05-04 惠生工程(中国)有限公司 Large-scale axial multistage-mixing heat exchange type oxydehydrogenation reactor for butylene

Similar Documents

Publication Publication Date Title
EP3402772B1 (en) Methanol process
RU2560363C2 (en) Hydrocarbon reforming method
EP1977993B1 (en) Catalytic steam reforming with recycle
RU2707088C2 (en) Method and system for producing methanol using partial oxidation
EP2676924A1 (en) Process for Reforming Hydrocarbons
US9561968B2 (en) Methods and systems for producing and processing syngas in a pressure swing adsorption unit and making ammonia therefrom
GB2550993A (en) Methanol process
WO2014056535A1 (en) Process for the production of synthesis gas
CA2910356A1 (en) A process for producing ammonia synthesis gas with high temperature shift and low steam-to-carbon ratio
KR20140111677A (en) Co-production of methanol and urea
AU2013279683B2 (en) Process for reforming hydrocarbons and process for starting up a gas -to-liquid process
RU2510883C2 (en) Method of obtaining synthesis-gas for ammonia production
WO2012084135A1 (en) Process for reforming hydrocarbon
CA2938779C (en) Process for producing synthesis gas by catalytic steam reforming of hydrocarbon feedstock
US8906266B2 (en) Process for the preparation of hydrogen and carbon monoxide containing gas
CN107406780B (en) Process for producing substitute natural gas
WO2015181214A1 (en) Increasing co/co2 ratio in syngas by reverse water gas shift
WO2018096018A1 (en) Multi bed reactor comprising an adiabatic and a heated catalyst bed
US10000379B2 (en) Process for the preparation of syngas
EP3659965B1 (en) Method for the production of steam in a steam reforming plant
RU2782258C2 (en) Method for production of methanol and ammonia
NZ743349B2 (en) Methanol process
WO2016139451A1 (en) Process for producing a substitute natural gas
US9683176B2 (en) Process for conversion of natural gas to liquid hydrocarbons and a plant for carrying out the process
CA2869068A1 (en) Process and apparatus for the parallel production of different synthesis gases

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17811486

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 17811486

Country of ref document: EP

Kind code of ref document: A1