WO2006063754A1 - Reactor for a catalytic conversion reaction - Google Patents

Reactor for a catalytic conversion reaction Download PDF

Info

Publication number
WO2006063754A1
WO2006063754A1 PCT/EP2005/013284 EP2005013284W WO2006063754A1 WO 2006063754 A1 WO2006063754 A1 WO 2006063754A1 EP 2005013284 W EP2005013284 W EP 2005013284W WO 2006063754 A1 WO2006063754 A1 WO 2006063754A1
Authority
WO
WIPO (PCT)
Prior art keywords
catalyst
support plate
catalyst support
reactor
perforated
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/EP2005/013284
Other languages
French (fr)
Inventor
Niels Erikstrup
Søren Gyde THOMSEN
Michael Boe
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
Priority to KR1020077013166A priority Critical patent/KR101278115B1/en
Priority to PL05818933T priority patent/PL1827672T3/en
Priority to JP2007545913A priority patent/JP5448342B2/en
Priority to EP05818933A priority patent/EP1827672B1/en
Priority to CA2590411A priority patent/CA2590411C/en
Priority to US11/792,289 priority patent/US7794676B2/en
Application filed by Haldor Topsoe AS filed Critical Haldor Topsoe AS
Priority to AU2005315872A priority patent/AU2005315872B2/en
Priority to ES05818933T priority patent/ES2397164T3/en
Priority to MX2007006887A priority patent/MX2007006887A/en
Publication of WO2006063754A1 publication Critical patent/WO2006063754A1/en
Anticipated expiration legal-status Critical
Priority to NO20073646A priority patent/NO20073646L/en
Ceased legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02—Chemical 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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02—Chemical 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
    • B01J8/0242—Chemical 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 flow within the bed being predominantly vertical
    • B01J8/025—Chemical 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 flow within the bed being predominantly vertical in a cylindrical shaped bed
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/008—Details of the reactor or of the particulate material; Processes to increase or to retard the rate of reaction
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02—Chemical 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
    • B01J8/0285—Heating or cooling the reactor
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen; Reversible storage of hydrogen
    • C01B3/02—Production of hydrogen; Production of gaseous mixtures containing hydrogen
    • C01B3/32—Production of hydrogen; Production of gaseous mixtures containing hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide or air
    • C01B3/34—Production of hydrogen; Production of gaseous mixtures containing hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide or air by reaction of hydrocarbons with gasifying agents
    • C01B3/38—Production of hydrogen; Production of gaseous mixtures containing hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide or air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/384—Production of hydrogen; Production of gaseous mixtures containing hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide or air by reaction of hydrocarbons with gasifying agents using catalysts with external heating of the catalyst
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008—Controlling the process
    • B01J2208/00017—Controlling the temperature
    • B01J2208/00106—Controlling the temperature by indirect heat exchange
    • B01J2208/00115—Controlling the temperature by indirect heat exchange with heat exchange elements inside the bed of solid particles
    • B01J2208/00132—Tubes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00796—Details of the reactor or of the particulate material
    • B01J2208/00884—Means for supporting the bed of particles, e.g. grids, bars, perforated plates
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02—Processes for making hydrogen or synthesis gas
    • C01B2203/0205—Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0227—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
    • C01B2203/0233—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a steam reforming step
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08—Methods of heating or cooling
    • C01B2203/0805—Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0838—Methods of heating the process for making hydrogen or synthesis gas by heat exchange with exothermic reactions, other than by combustion of fuel
    • C01B2203/0844—Methods of heating the process for making hydrogen or synthesis gas by heat exchange with exothermic reactions, other than by combustion of fuel the non-combustive exothermic reaction being another reforming reaction as defined in groups C01B2203/02 - C01B2203/0294
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/16—Controlling the process
    • C01B2203/1604—Starting up the process
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/16—Controlling the process
    • C01B2203/1609—Shutting down the process
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Definitions

  • the invention relates to a catalytic reactor that is constructed to reduce deformation and rupture of the reactor internals .
  • a catalytic reactor with an improved catalyst housing.
  • the chemical reaction is often catalysed by solid catalyst particles.
  • These catalyst particles are typically located in catalyst beds, and during passage of a reactive fluid through the catalyst bed, a chemical reaction takes place, thereby con- verting the reactive fluid into the desired product or mixture of products having a chemical composition different from that of the reactive fluid.
  • reactor in- ternals The inner contents of a reactor are known as reactor in- ternals.
  • the catalyst bed is kept in position in the reactor by reactor internals which allow fluid passage to and from the catalyst particles. This is commonly done by perforating the reactor internals in contact with the catalyst particles. The nature of the perforation determines the fluid flow pattern inside the catalyst bed.
  • the reactor internals for keeping the catalyst bed in position are typically a catalyst support plate supported along its edges and/or on the free side opposite the cata- lyst side. In some cases it is not feasible to support the catalyst support plate on this free side, as for example is the case when the catalyst particles and the catalyst support plate undergo large movement due to thermal expansion of the internals.
  • the catalyst bed can typically have a free upper surface and a bottom surface supported by a horizontal catalyst support plate with perforations.
  • the catalyst bed is kept in place by the vertical non-perforated walls of the catalyst housing and by the perforated catalyst support plate. Gas then enters the catalyst bed from the free upper sur- face side and leaves the catalyst bed through the perforated catalyst support plate at the bottom of the catalyst bed.
  • the catalyst support plate is fixed along its edge to the vertical catalyst housing wall and is typically not supported on its free side from below.
  • An alternative method of supporting the catalyst support plate is by using various supporting structures placed in the catalyst bed and fixed on the catalyst support plate. This allows the use of larger catalyst support plates in comparison to fixing the support plate to the catalyst housing walls. Supporting structures such as stays fixed on the catalyst support plate can be used. Stays are supportive elements fixed at one end to a first structure and at its other end to a second structure, providing support to one or both of the structures.
  • stays and such similar supporting structures can have differences in thermal expansion due to unequal temperature distribution in the reactor. This causes high stress effects within the catalyst support plate and in the stays in the axial direction, and this can lead to their deformation or rupture. The forces experienced by these particular reactor internals in the radial direction are negligible compared to the forces in the axial direc- tion.
  • the English abstract of JP patent application No. 49010172 discloses a catalytic reaction apparatus useful in high temperature catalytic reactions for avoiding rupture of the catalyst supporting plate.
  • the catalyst supporting plate has holes and is partitioned into one or more regions and a supporter for the catalyst-supporting plate. Both are fastened with vertical bolts. The thermal expansion of the catalyst supporting plate can be absorbed by loosening the bolts between the plate and its supporter so that they can slide relative to each other.
  • This application describes a catalytic reaction apparatus in which the stresses in the catalyst supporting plate are reduced in the radial direction only. There is no mention of how to reduce the stresses in the axial direction. It is therefore an objective of the invention to provide a catalytic reactor in which thermal stresses on the reactor internals in the axial direction are reduced. This in turn reduces deformation and rupture of the reactor internals.
  • the invention comprises a catalytic reactor having reactor internals which include a segmented catalytic support plate supported by elongated support elements, in which the stresses experienced by the reactor internals at higher temperatures are reduced in the axial direction.
  • the invention comprises a catalytic reactor having the characteristics described in claim 1.
  • Figs. 1, 2 and 3 are schematic diagrams showing transverse sections of the segmented catalyst support plate in three different embodiments of the invention.
  • Fig. 4 is a schematic diagram showing a longitudinal sec- tion through the catalyst housing with stays fixed at their lower ends to the segmented catalyst support plate.
  • Fig. 5 is a schematic diagram showing a longitudinal section through the catalyst housing with tubes fixed at their lower ends to the segmented catalyst support plate.
  • Fig. 6 is a schematic diagram showing a longitudinal sec- tion through the catalyst housing with double tubes fixed at their lower ends to the segmented catalyst support plate .
  • Fig. 7 is a schematic diagram showing a transverse section of the segmented catalyst support plate with segments attached either to the catalyst housing wall or to the elongated support elements.
  • the catalytic reactor of the invention includes a catalyst housing comprising a plurality of elongated support elements.
  • a perforated cata- lyst support plate for supporting a bed of catalyst particles.
  • the elongated support elements are, at their lower ends, fixed to the perforated catalyst support plate, for instance by means of welding.
  • the perforated catalyst support plate is segmented and each catalyst support plate segment is supported by an elongated support element.
  • the assembly consisting of segmented catalyst support plate and elongated support elements fixed on these catalyst support plate segments are supported by a tube sheet or plate onto which the upper ends of the elongated support elements are fixed.
  • the catalytic bed is positioned on the upper surface of the perforated catalyst support plate.
  • Catalyst particles thus surround the outer surface of the elongated support elements.
  • Process gas entering the catalytic reactor is directed towards the catalytic bed for reaction.
  • the perforations in the catalyst support plate allow the reacted process gas to flow through both the catalyst bed and the catalyst support plate to the lower side of the catalyst support plate.
  • the segmented catalyst support plate can for instance be prepared by cutting a single, large, catalyst support plate having the required dimensions suitable for the reactor apparatus into smaller individual catalyst support plate segments .
  • the catalyst support plate can be cut using, for instance, water jet cutting or any other suitable method known in the art. Perforations can be made in the catalyst support plate segments or the large catalyst support plate can already be perforated before cutting it into individual segments.
  • the catalyst support plate segments can have any suitable shape or combination of shapes which can be placed in the reaction apparatus to form a surface on which the catalyst bed can be positioned.
  • the catalyst support plate segments can for instance be three-sided (triangular) , four-sided, five-sided or six-sided.
  • the catalyst support plate segments can be placed beside each other edge to edge, with or without a gap between the plate segments. If a gap is present then it is important that the catalyst particles are prevented from falling through the aperture into the volume below the catalyst support plate.
  • each catalyst support plate segment should be, under all process, start-up and shut-down conditions, at least equal to the largest possible difference in extension between two neighbouring elongated support elements .
  • the segmented catalyst support plate can be made of any suitable material . Examples are nickel alloys and stainless steel.
  • the elongated support elements can have a transverse cross- section that is cylindrical.
  • Other cross-sectional shapes are also possible, e.g. a hexagonal or square cross- section.
  • the transverse cross-section can be polygonal in shape.
  • the catalytic reactor of the invention is suitable for use at a wide range of temperatures. It is particularly suitable for use at temperatures above 700°C in reactors, where the stays can experience a large variation in temperatures leading to significant variations in thermal ex- pansion.
  • Each catalyst support plate segment is attached to at least one elongated support element.
  • catalyst support plate segments bordering the wall of the catalyst housing can optionally be fixed to this wall while the remaining catalyst support plate segments are attached to the lower ends of the elongated support elements.
  • An embodiment of the invention is a catalytic reactor in which the elongated support elements are stays onto which the catalyst support plate segments are attached.
  • Another embodiment of the invention is the catalytic reactor in which the elongated support elements are tubes e.g. heat transfer tubes onto which the catalyst support plate segments are attached.
  • an embodiment of the invention is the catalytic reactor in which the elongated support elements onto which the catalyst support plate segments are attached are concentric double tubes e.g. with catalyst inside the inner tu- be.
  • the annular volume, that is the annulus, is the concentric double tubes, provides a channel that can for instance be useful in the transfer of process gas.
  • Fig. 1 is a schematic diagram showing a transverse section of a segmented catalyst support plate 1.
  • the catalyst support plate 1 is cut into several seg- ments consisting of a central catalyst support plate segment 2 and peripheral catalyst support plate segments 3 that are correspondingly supported by a centrally placed elongated support element placed in the hole 4 and peripheral elongated support elements placed in hole 5.
  • Each catalyst support plate segment has perforations 6 that provide even distribution of the process gas through both the catalyst bed and the catalyst support plate segments.
  • the catalyst support plate segments 2 and 3 are respectively four and six sided.
  • each catalytic support plate segment can be cut in different shapes as illustrated in Fig. 2.
  • Fig. 2 shows a transverse section through a catalyst housing in a catalytic reactor of the invention comprising a plurality of elongated support elements 4 fixed to a plurality of catalyst support plate segments 2 and 3 with perforations 6.
  • This embodiment shows catalyst support plate segments 2 and 3 that are respectively hexagonal and pentagonal in shape, and the length of the sides of the catalyst support plate segments can vary i.e. they are not identical in length, as shown in catalyst support plate segment 2.
  • Catalyst support plate segments that are triangular or square in shape are also useful in the catalytic reactor of the invention.
  • the catalyst support plate segments 2 can therefore be polygonal in shape.
  • the elongated support elements are cylindrical and consist of concentric double tubes.
  • Fig. 3 shows a variation of the embodiment shown in Fig. 1.
  • the central catalyst support plate segment is eliminated and the peripheral catalyst support plate segments 3 are cut such that they border the central elongated element placed in hole 4.
  • the central elongated element in hole 4 does not support any of the catalyst support plate segments 3.
  • All the catalyst support plate segments are supported. However not all the elongated elements in the catalyst bed provide support to a catalyst support plate segment.
  • the number of the elongated support elements can vary in accordance with the size of the reactor, but will mostly be in the range 1 to 1000. Elongated elements not providing support could be tubes for transport of fluids .
  • FIG. 4 shows a longitudinal section through a catalytic reactor 1 of the invention.
  • the catalytic reactor 1 includes a catalyst housing 2 and a plurality of stays 3 which are arrayed inside the housing 2. Two stays 3 are shown.
  • Each stay 3 supports a catalyst support plate segment 4 at the lower end of the stay.
  • the plate segments 4 have perforations 5 and are placed edge to edge with or without a gap 6 between the edges of the plate segments 4.
  • the plate segments 4 thus form a surface similar to that of a single large catalyst support plate suitable for supporting the catalyst bed 7.
  • Process gas enters the catalyst housing 2 through the inlet 8, and passes through the catalyst bed 7 for catalytic reaction at the required temperature. After catalytic reaction the process gas passes through the perfora- tions 5 and the gaps 6, if present, to enter the volume 9 downstream the catalyst bed 7.
  • FIG. 5 Another embodiment of the invention is shown in Fig. 5.
  • the catalytic reactor of the invention is similar to that described in Fig. 4 with the exception that the elongated support elements are tubes 3 through which a process fluid can flow with the lower ends of the tubes being fixed to the catalyst support plate segments 4. Only the catalyst housing and its contents are shown in this figure.
  • a process fluid enters the catalyst housing 2 through the inlet 8 and is converted during passage through the catalyst bed 7.
  • the reacted process gas enters the volume 9 and thereafter the tubes 3 through their lower ends.
  • the reacted process gas can be in indirect heat exchange with the reacting process gas in the catalyst bed 7.
  • This embodiment is suitable for use in a steam reforming reaction in which methane is reacted with steam to produce carbon monoxide and hydrogen.
  • the endothermic steam reforming reaction takes place in the catalyst bed 7, and the product gas enters volume 9 and is mixed with hot gas entering from inlet 10. The mixture is thereafter, during transfer through the tubes 3, cooled by heat exchange with the reaction occurring in catalyst bed 7. The reacted gas leaves the catalyst housing 2 through the outlet 12.
  • Fig. 5 is particularly useful in steam reforming reactions where temperatures as high as 1000 0 C are experienced.
  • a reactor tube which can be twelve meters in length, can experience an expansion in length of, for instance, 160 millimetres at this temperature, depending on the coefficient of thermal expansion of the tube metal. Since the reactor tube is fixed at its upper end to the tube sheet 11, the expansion is largest at its lower end.
  • FIG. 6 A further embodiment of the invention is shown in Fig. 6. Only the catalyst housing and its contents are shown in this figure.
  • the catalytic reactor of the invention is similar to that described in Fig. 5 with the exception that the elongated support elements are concentric double tubes 3 with their outer tube fixed at their lower ends to the catalyst support plate segments 4.
  • a process fluid can flow in the annulus 5 of the concentric double tubes 3 and the volume of the inner tube 6 can be filled with catalyst particles.
  • the segmented catalyst support plates 4 support the catalytic bed 7 outside the concentric double tubes 3.
  • a process fluid for instance process gas
  • the process gas is simultaneously converted during passage through catalyst bed 7 located outside the concentric double tubes 3.
  • the converted process gas leaves the volume 13 of the inner tube 6 of the concentric double tube 3 and enters the volume 9.
  • the converted process gas also leaves the catalyst bed 7 through the perforated segmented catalyst support plate 4 and enters the volume 9.
  • the converted process gas in volume 9 can then be mixed with another gas entering catalyst housing 2 through inlet 10.
  • the process gas mixture is thereafter transferred through the annulus 5 of the concentric double tubes 3 to the outlet 12.
  • Another preferable embodiment of the invention is the catalytic reactor in which the catalyst support plate segments are fixed to either an elongated support element or to the vertical wall of the catalyst housing as shown in Fig. 7.
  • some of the catalyst support plate segments 1 bordering the vertical wall of the catalyst housing are fixed to and supported by the vertical wall.
  • the remaining catalyst support plate segments 2 are fixed to and supported by elongated support elements placed in the hole 3.

Landscapes

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

Abstract

Reactor for a catalytic conversion reaction comprising within a catalyst housing a perforated catalyst support plate supporting a catalyst bed, the perforated catalyst support plate being supported by a plurality of elongated support elements, and catalyst particles in the catalyst bed being placed outside the elongated support elements, the perforated catalyst support plate being attached to the lower ends of the elongated support elements, the perfo­rated catalyst support plate being divided into a plurality of perforated catalyst support plate segments, at least one perforated catalyst support plate segment being supported by an elongated support element.

Description

REACTOR FOR A CATALYTIC CONVERSION REACTION
The invention relates to a catalytic reactor that is constructed to reduce deformation and rupture of the reactor internals . In particular it relates to a catalytic reactor with an improved catalyst housing.
BACKGROUND OF THE INVENTION
In heterogeneous chemical reactions the chemical reaction is often catalysed by solid catalyst particles. These catalyst particles are typically located in catalyst beds, and during passage of a reactive fluid through the catalyst bed, a chemical reaction takes place, thereby con- verting the reactive fluid into the desired product or mixture of products having a chemical composition different from that of the reactive fluid.
The inner contents of a reactor are known as reactor in- ternals. The catalyst bed is kept in position in the reactor by reactor internals which allow fluid passage to and from the catalyst particles. This is commonly done by perforating the reactor internals in contact with the catalyst particles. The nature of the perforation determines the fluid flow pattern inside the catalyst bed.
The reactor internals for keeping the catalyst bed in position are typically a catalyst support plate supported along its edges and/or on the free side opposite the cata- lyst side. In some cases it is not feasible to support the catalyst support plate on this free side, as for example is the case when the catalyst particles and the catalyst support plate undergo large movement due to thermal expansion of the internals.
The catalyst bed can typically have a free upper surface and a bottom surface supported by a horizontal catalyst support plate with perforations. The catalyst bed is kept in place by the vertical non-perforated walls of the catalyst housing and by the perforated catalyst support plate. Gas then enters the catalyst bed from the free upper sur- face side and leaves the catalyst bed through the perforated catalyst support plate at the bottom of the catalyst bed. The catalyst support plate is fixed along its edge to the vertical catalyst housing wall and is typically not supported on its free side from below. When the reactor is heated up, thermal expansion of the catalyst bed and the vertical walls of the catalyst housing or other reactor internals cause a deformation of the catalyst bed and the reactor internals in a downward axial direction.
During passage of the reactive fluid across the catalyst bed and catalyst support plate, the reactive fluid experiences a pressure drop and this, combined with the weight of the catalyst particles on the catalyst plate, can cause deformation of the catalyst support plate. There exists therefore an upper limit for the surface area of the support plate when the catalyst support plate is only supported along its edges. Proceeding above this upper limit would demand an impractical or uneconomical reinforcement of the catalyst support plate for instance the use of a very thick catalyst support plate. An alternative method of supporting the catalyst support plate is by using various supporting structures placed in the catalyst bed and fixed on the catalyst support plate. This allows the use of larger catalyst support plates in comparison to fixing the support plate to the catalyst housing walls. Supporting structures such as stays fixed on the catalyst support plate can be used. Stays are supportive elements fixed at one end to a first structure and at its other end to a second structure, providing support to one or both of the structures.
However, stays and such similar supporting structures can have differences in thermal expansion due to unequal temperature distribution in the reactor. This causes high stress effects within the catalyst support plate and in the stays in the axial direction, and this can lead to their deformation or rupture. The forces experienced by these particular reactor internals in the radial direction are negligible compared to the forces in the axial direc- tion.
The English abstract of JP patent application No. 49010172 discloses a catalytic reaction apparatus useful in high temperature catalytic reactions for avoiding rupture of the catalyst supporting plate. The catalyst supporting plate has holes and is partitioned into one or more regions and a supporter for the catalyst-supporting plate. Both are fastened with vertical bolts. The thermal expansion of the catalyst supporting plate can be absorbed by loosening the bolts between the plate and its supporter so that they can slide relative to each other. This application describes a catalytic reaction apparatus in which the stresses in the catalyst supporting plate are reduced in the radial direction only. There is no mention of how to reduce the stresses in the axial direction. It is therefore an objective of the invention to provide a catalytic reactor in which thermal stresses on the reactor internals in the axial direction are reduced. This in turn reduces deformation and rupture of the reactor internals.
BRIEF SUMMARY OF THE INVENTION
The invention comprises a catalytic reactor having reactor internals which include a segmented catalytic support plate supported by elongated support elements, in which the stresses experienced by the reactor internals at higher temperatures are reduced in the axial direction.
The invention comprises a catalytic reactor having the characteristics described in claim 1.
BRIEF DESCRIPTION OF THE DRAWINGS
Figs. 1, 2 and 3 are schematic diagrams showing transverse sections of the segmented catalyst support plate in three different embodiments of the invention.
Fig. 4 is a schematic diagram showing a longitudinal sec- tion through the catalyst housing with stays fixed at their lower ends to the segmented catalyst support plate. Fig. 5 is a schematic diagram showing a longitudinal section through the catalyst housing with tubes fixed at their lower ends to the segmented catalyst support plate. Fig. 6 is a schematic diagram showing a longitudinal sec- tion through the catalyst housing with double tubes fixed at their lower ends to the segmented catalyst support plate .
Fig. 7 is a schematic diagram showing a transverse section of the segmented catalyst support plate with segments attached either to the catalyst housing wall or to the elongated support elements.
DETAILED DESCRIPTION OF THE INVENTION
The catalytic reactor of the invention includes a catalyst housing comprising a plurality of elongated support elements. Within the catalyst housing is a perforated cata- lyst support plate for supporting a bed of catalyst particles. The elongated support elements are, at their lower ends, fixed to the perforated catalyst support plate, for instance by means of welding. The perforated catalyst support plate is segmented and each catalyst support plate segment is supported by an elongated support element. The assembly consisting of segmented catalyst support plate and elongated support elements fixed on these catalyst support plate segments are supported by a tube sheet or plate onto which the upper ends of the elongated support elements are fixed. The catalytic bed is positioned on the upper surface of the perforated catalyst support plate. Catalyst particles thus surround the outer surface of the elongated support elements. Process gas entering the catalytic reactor is directed towards the catalytic bed for reaction. The perforations in the catalyst support plate allow the reacted process gas to flow through both the catalyst bed and the catalyst support plate to the lower side of the catalyst support plate.
The segmented catalyst support plate can for instance be prepared by cutting a single, large, catalyst support plate having the required dimensions suitable for the reactor apparatus into smaller individual catalyst support plate segments . The catalyst support plate can be cut using, for instance, water jet cutting or any other suitable method known in the art. Perforations can be made in the catalyst support plate segments or the large catalyst support plate can already be perforated before cutting it into individual segments.
The catalyst support plate segments can have any suitable shape or combination of shapes which can be placed in the reaction apparatus to form a surface on which the catalyst bed can be positioned. The catalyst support plate segments can for instance be three-sided (triangular) , four-sided, five-sided or six-sided.
The catalyst support plate segments can be placed beside each other edge to edge, with or without a gap between the plate segments. If a gap is present then it is important that the catalyst particles are prevented from falling through the aperture into the volume below the catalyst support plate.
In order to avoid this situation, the minimum thickness of each catalyst support plate segment should be, under all process, start-up and shut-down conditions, at least equal to the largest possible difference in extension between two neighbouring elongated support elements .
The segmented catalyst support plate can be made of any suitable material . Examples are nickel alloys and stainless steel.
The elongated support elements can have a transverse cross- section that is cylindrical. Other cross-sectional shapes are also possible, e.g. a hexagonal or square cross- section. In other words, the transverse cross-section can be polygonal in shape.
The catalytic reactor of the invention is suitable for use at a wide range of temperatures. It is particularly suitable for use at temperatures above 700°C in reactors, where the stays can experience a large variation in temperatures leading to significant variations in thermal ex- pansion.
Each catalyst support plate segment is attached to at least one elongated support element. However, catalyst support plate segments bordering the wall of the catalyst housing can optionally be fixed to this wall while the remaining catalyst support plate segments are attached to the lower ends of the elongated support elements. An embodiment of the invention is a catalytic reactor in which the elongated support elements are stays onto which the catalyst support plate segments are attached.
Another embodiment of the invention is the catalytic reactor in which the elongated support elements are tubes e.g. heat transfer tubes onto which the catalyst support plate segments are attached.
Yet an embodiment of the invention is the catalytic reactor in which the elongated support elements onto which the catalyst support plate segments are attached are concentric double tubes e.g. with catalyst inside the inner tu- be. The annular volume, that is the annulus, is the concentric double tubes, provides a channel that can for instance be useful in the transfer of process gas.
The invention and its embodiments are described in more detail in the following:
Fig. 1 is a schematic diagram showing a transverse section of a segmented catalyst support plate 1. In this embodiment, the catalyst support plate 1 is cut into several seg- ments consisting of a central catalyst support plate segment 2 and peripheral catalyst support plate segments 3 that are correspondingly supported by a centrally placed elongated support element placed in the hole 4 and peripheral elongated support elements placed in hole 5. Each catalyst support plate segment has perforations 6 that provide even distribution of the process gas through both the catalyst bed and the catalyst support plate segments. In this embodiment the catalyst support plate segments 2 and 3 are respectively four and six sided.
However, each catalytic support plate segment can be cut in different shapes as illustrated in Fig. 2. Fig. 2 shows a transverse section through a catalyst housing in a catalytic reactor of the invention comprising a plurality of elongated support elements 4 fixed to a plurality of catalyst support plate segments 2 and 3 with perforations 6. This embodiment shows catalyst support plate segments 2 and 3 that are respectively hexagonal and pentagonal in shape, and the length of the sides of the catalyst support plate segments can vary i.e. they are not identical in length, as shown in catalyst support plate segment 2. Catalyst support plate segments that are triangular or square in shape are also useful in the catalytic reactor of the invention. The catalyst support plate segments 2 can therefore be polygonal in shape. In this embodiment the elongated support elements are cylindrical and consist of concentric double tubes.
Fig. 3 shows a variation of the embodiment shown in Fig. 1. In this embodiment, the central catalyst support plate segment is eliminated and the peripheral catalyst support plate segments 3 are cut such that they border the central elongated element placed in hole 4. In this case, the central elongated element in hole 4 does not support any of the catalyst support plate segments 3.
All the catalyst support plate segments are supported. However not all the elongated elements in the catalyst bed provide support to a catalyst support plate segment. The number of the elongated support elements can vary in accordance with the size of the reactor, but will mostly be in the range 1 to 1000. Elongated elements not providing support could be tubes for transport of fluids .
In practice the temperature differences experienced across the total surface of the catalyst support plate segments can vary widely. However, the local temperature differences between neighbouring elongated support elements are not large. This means that the expansion experienced locally by neighbouring elongated support elements is very similar. Any elongated support elements therefore expand by approximately the same length as its nearest neighbours.
Another embodiment of the invention is shown in Fig. 4. Fig. 4 shows a longitudinal section through a catalytic reactor 1 of the invention. The catalytic reactor 1 includes a catalyst housing 2 and a plurality of stays 3 which are arrayed inside the housing 2. Two stays 3 are shown. Each stay 3 supports a catalyst support plate segment 4 at the lower end of the stay. The plate segments 4 have perforations 5 and are placed edge to edge with or without a gap 6 between the edges of the plate segments 4.
The plate segments 4 thus form a surface similar to that of a single large catalyst support plate suitable for supporting the catalyst bed 7.
Process gas enters the catalyst housing 2 through the inlet 8, and passes through the catalyst bed 7 for catalytic reaction at the required temperature. After catalytic reaction the process gas passes through the perfora- tions 5 and the gaps 6, if present, to enter the volume 9 downstream the catalyst bed 7.
Another embodiment of the invention is shown in Fig. 5. In this embodiment the catalytic reactor of the invention is similar to that described in Fig. 4 with the exception that the elongated support elements are tubes 3 through which a process fluid can flow with the lower ends of the tubes being fixed to the catalyst support plate segments 4. Only the catalyst housing and its contents are shown in this figure. A process fluid enters the catalyst housing 2 through the inlet 8 and is converted during passage through the catalyst bed 7. After passage through plate segments 4 the reacted process gas enters the volume 9 and thereafter the tubes 3 through their lower ends. During passage through the tubes 3 the reacted process gas can be in indirect heat exchange with the reacting process gas in the catalyst bed 7.
This embodiment is suitable for use in a steam reforming reaction in which methane is reacted with steam to produce carbon monoxide and hydrogen. The endothermic steam reforming reaction takes place in the catalyst bed 7, and the product gas enters volume 9 and is mixed with hot gas entering from inlet 10. The mixture is thereafter, during transfer through the tubes 3, cooled by heat exchange with the reaction occurring in catalyst bed 7. The reacted gas leaves the catalyst housing 2 through the outlet 12.
The embodiment shown in Fig. 5 is particularly useful in steam reforming reactions where temperatures as high as 10000C are experienced. In such reactors a reactor tube, which can be twelve meters in length, can experience an expansion in length of, for instance, 160 millimetres at this temperature, depending on the coefficient of thermal expansion of the tube metal. Since the reactor tube is fixed at its upper end to the tube sheet 11, the expansion is largest at its lower end.
An unequal temperature distribution in the reactor can lead to a variation in the expansion of each individual reactor tube in the reactor. Ultimately this will result in deformation and rupture of the catalyst support plate if it is not segmented. When the segmented catalyst support plate is used, it allows differential expansion of the reactor tubes without rupture of any of the internals.
A further embodiment of the invention is shown in Fig. 6. Only the catalyst housing and its contents are shown in this figure. In this embodiment the catalytic reactor of the invention is similar to that described in Fig. 5 with the exception that the elongated support elements are concentric double tubes 3 with their outer tube fixed at their lower ends to the catalyst support plate segments 4. A process fluid can flow in the annulus 5 of the concentric double tubes 3 and the volume of the inner tube 6 can be filled with catalyst particles. The segmented catalyst support plates 4 support the catalytic bed 7 outside the concentric double tubes 3.
Fig. 6 is explained in more detail in the following. A process fluid, for instance process gas, enters the catalyst housing 2 through the inlet 8 and is converted during passage through the additional catalyst bed 11 located in the volume 13 of the inner tube 6 of the concentric double tube 3. The process gas is simultaneously converted during passage through catalyst bed 7 located outside the concentric double tubes 3. The converted process gas leaves the volume 13 of the inner tube 6 of the concentric double tube 3 and enters the volume 9. The converted process gas also leaves the catalyst bed 7 through the perforated segmented catalyst support plate 4 and enters the volume 9. The converted process gas in volume 9 can then be mixed with another gas entering catalyst housing 2 through inlet 10. The process gas mixture is thereafter transferred through the annulus 5 of the concentric double tubes 3 to the outlet 12.
Another preferable embodiment of the invention is the catalytic reactor in which the catalyst support plate segments are fixed to either an elongated support element or to the vertical wall of the catalyst housing as shown in Fig. 7. In this embodiment some of the catalyst support plate segments 1 bordering the vertical wall of the catalyst housing are fixed to and supported by the vertical wall. The remaining catalyst support plate segments 2 are fixed to and supported by elongated support elements placed in the hole 3.

Claims

1. Reactor for a catalytic conversion reaction comprising within a catalyst housing a perforated catalyst support plate supporting a catalyst bed, the catalyst support plate being supported by a plurality of elongated support elements, the catalyst particles in the catalyst bed being placed outside the elongated support elements, the perforated catalyst support plate being attached to the lower ends of the elongated support elements, the perforated catalyst support plate being divided into a plurality of perforated catalyst support plate segments, at least one perforated catalyst support plate segment being supported by an elongated support element.
2. Reactor according to claim 1 wherein at least one further catalyst support plate segment bordering the wall of the catalyst housing is supported by this wall.
3. Reactor according to claim 1 wherein the elongated support elements have a cylindrical or polygonal cross section.
5. Reactor according to anyone of claims 1-4, wherein the elongated support elements are stays, tubes or concentric double tubes.
6. Reactor according to claim 5, wherein the tubes are heat transfer tubes. 7. Reactor according to claim 5, wherein the concentric double tubes contain catalyst inside the inner tube and process gas in the annulus .
8. Reactor according to claims 1 - 3, wherein the catalyst support plate segments are polygonal in shape.
9. Use of the reactor according to anyone of claims 1 to 9 in a steam reforming reaction.
PCT/EP2005/013284 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction Ceased WO2006063754A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
AU2005315872A AU2005315872B2 (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction
PL05818933T PL1827672T3 (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction
JP2007545913A JP5448342B2 (en) 2004-12-17 2005-12-12 Reactor for catalytic conversion reaction
EP05818933A EP1827672B1 (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction
CA2590411A CA2590411C (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction
KR1020077013166A KR101278115B1 (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction
MX2007006887A MX2007006887A (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction.
US11/792,289 US7794676B2 (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction
ES05818933T ES2397164T3 (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction
NO20073646A NO20073646L (en) 2004-12-17 2007-07-16 Reactor for a catalytic conversion reaction

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DKPA200401951 2004-12-17
DKPA200401951 2004-12-17

Publications (1)

Publication Number Publication Date
WO2006063754A1 true WO2006063754A1 (en) 2006-06-22

Family

ID=35788726

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2005/013284 Ceased WO2006063754A1 (en) 2004-12-17 2005-12-12 Reactor for a catalytic conversion reaction

Country Status (15)

Country Link
US (1) US7794676B2 (en)
EP (1) EP1827672B1 (en)
JP (1) JP5448342B2 (en)
KR (1) KR101278115B1 (en)
CN (2) CN103537232A (en)
AR (1) AR052816A1 (en)
AU (1) AU2005315872B2 (en)
CA (1) CA2590411C (en)
ES (1) ES2397164T3 (en)
MX (1) MX2007006887A (en)
NO (1) NO20073646L (en)
PL (1) PL1827672T3 (en)
RU (1) RU2399411C2 (en)
WO (1) WO2006063754A1 (en)
ZA (1) ZA200704891B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2417834C1 (en) * 2009-10-09 2011-05-10 Андрей Юрьевич Беляев Convector for gas-phase catalytic processes
RU2419485C1 (en) * 2009-11-17 2011-05-27 Андрей Юрьевич Беляев Convector for gas phase catalytic processes and gas phase catalytic process convector thermal element
EP2556886A4 (en) * 2010-04-05 2014-05-21 Amogreentech Co Ltd HIGH CAPACITY METAL CATALYST SUPPORT AND CATALYTIC CONVERTER USING THE SAME

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9636652B2 (en) * 2013-12-05 2017-05-02 Exxonmobil Research And Engineering Company Reactor bed vessel and support assembly
CN105561887A (en) * 2014-10-10 2016-05-11 天津汇康源科技有限公司 Catalytic reaction structure of chemical reactor
CN107243297A (en) * 2017-07-24 2017-10-13 德艾柯工程技术（上海）有限公司 A kind of board-like modularization temperature control reactor
ES2925579T3 (en) * 2018-12-19 2022-10-18 Topsoe As Catalytic reactor with charge distributor assembly
US10478794B1 (en) 2019-02-26 2019-11-19 Chevron Phillips Chemical Company Lp Bi-modal radial flow reactor
CN114713145B (en) * 2020-12-22 2023-01-10 中国石油化工股份有限公司 Filling method of graded catalyst
WO2026012935A1 (en) * 2024-07-08 2026-01-15 Topsoe A/S Multiple-bed catalytic reactor comprising sandwich tube sheet

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4910172A (en) 1972-05-30 1974-01-29
US4195064A (en) 1978-08-15 1980-03-25 Monsanto Company Unitized catalytic reactor construction
US4743578A (en) * 1985-11-13 1988-05-10 Imperial Chemical Industries Plc Ceramic structures
WO2000040329A1 (en) 1999-01-08 2000-07-13 Imperial Chemical Industries Plc Catalyst support
WO2003086607A1 (en) * 2002-04-12 2003-10-23 Bp Chemicals Limited Support grid

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2291762A (en) * 1939-09-21 1942-08-04 Sun Oil Co Catalytic apparatus
CH449678A (en) * 1967-06-20 1968-01-15 Bertrams Ag Hch Tubular heat exchanger with liquid heat transfer medium
JPS49114581A (en) * 1973-03-05 1974-11-01
US4226830A (en) * 1978-08-28 1980-10-07 Hicap Engineering & Development Corporation Fluidized bed reactor
SU1184556A1 (en) * 1984-09-18 1985-10-15 Предприятие П/Я Р-6518 Reactor for cracking of hydrocarbon raw material
DE3532413A1 (en) * 1985-09-11 1987-03-12 Uhde Gmbh DEVICE FOR GENERATING SYNTHESIS GAS
JPS631436A (en) * 1986-06-20 1988-01-06 Mitsubishi Heavy Ind Ltd Catalyst holding apparatus
JPS631438A (en) * 1986-06-20 1988-01-06 Mitsubishi Heavy Ind Ltd Reactor
JPS6313238U (en) * 1986-07-09 1988-01-28
US4863699A (en) * 1988-02-05 1989-09-05 Shaw Donald J Grid with conical support skirt
JPH01261201A (en) * 1988-04-12 1989-10-18 Mitsubishi Gas Chem Co Inc Hydrocarbon reforming reactor
US5567398A (en) * 1990-04-03 1996-10-22 The Standard Oil Company Endothermic reaction apparatus and method
FR2660875B1 (en) * 1990-04-13 1992-08-14 Technip Cie CATALYTIC, TUBULAR AND PRESSURIZED HYDROCARBON CONVERTER.
JPH04141227A (en) * 1990-10-03 1992-05-14 Nagaoka Kinmo Kk Method and apparatus for holding catalyst in radial flow type catalyst packed tower
JPH04190843A (en) * 1990-11-22 1992-07-09 Toshiba Corp Gas reaction apparatus
CA2207922A1 (en) * 1994-11-17 1996-05-30 International Fuel Cells Corporation Catalytic reactor design to reduce catalyst slumping and crushing
DE10051008A1 (en) * 2000-10-14 2002-04-18 Glatt Ingtech Gmbh Fluidized bed used for drying, granulating, agglomerating and coating processes has fluidized bed segments separated by expansion joints with elastic element arranged below joint of each segment
CA2439544A1 (en) * 2001-03-01 2002-09-12 Shell Internationale Research Maatschappij B.V. Self-supporting reactor internal
JP2005132690A (en) * 2003-10-31 2005-05-26 Chiyoda Corp Activated carbon regenerator

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4910172A (en) 1972-05-30 1974-01-29
US4195064A (en) 1978-08-15 1980-03-25 Monsanto Company Unitized catalytic reactor construction
US4743578A (en) * 1985-11-13 1988-05-10 Imperial Chemical Industries Plc Ceramic structures
WO2000040329A1 (en) 1999-01-08 2000-07-13 Imperial Chemical Industries Plc Catalyst support
WO2003086607A1 (en) * 2002-04-12 2003-10-23 Bp Chemicals Limited Support grid

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2417834C1 (en) * 2009-10-09 2011-05-10 Андрей Юрьевич Беляев Convector for gas-phase catalytic processes
RU2419485C1 (en) * 2009-11-17 2011-05-27 Андрей Юрьевич Беляев Convector for gas phase catalytic processes and gas phase catalytic process convector thermal element
EP2556886A4 (en) * 2010-04-05 2014-05-21 Amogreentech Co Ltd HIGH CAPACITY METAL CATALYST SUPPORT AND CATALYTIC CONVERTER USING THE SAME
RU2598030C2 (en) * 2010-04-05 2016-09-20 Амогринтех Ко., Лтд. Substrate for metal catalyst of high power and catalytic converter using same

Also Published As

Publication number Publication date
JP2008523968A (en) 2008-07-10
AU2005315872A1 (en) 2006-06-22
AU2005315872B2 (en) 2010-05-20
CN101080266A (en) 2007-11-28
RU2007126962A (en) 2009-01-27
US20070264177A1 (en) 2007-11-15
EP1827672A1 (en) 2007-09-05
AR052816A1 (en) 2007-04-04
ES2397164T3 (en) 2013-03-05
NO20073646L (en) 2007-09-11
KR101278115B1 (en) 2013-06-24
ZA200704891B (en) 2008-09-25
JP5448342B2 (en) 2014-03-19
CN103537232A (en) 2014-01-29
KR20070086049A (en) 2007-08-27
RU2399411C2 (en) 2010-09-20
PL1827672T3 (en) 2013-04-30
MX2007006887A (en) 2007-06-22
CA2590411A1 (en) 2006-06-22
US7794676B2 (en) 2010-09-14
EP1827672B1 (en) 2012-11-28
CA2590411C (en) 2013-09-17

Similar Documents

Publication Publication Date Title
US8168131B2 (en) Low pressure drop reforming reactor
EP0025308B1 (en) A process and apparatus for catalytically reacting steam with a hydrocarbon in endothermic conditions
EP2249954B1 (en) Catalytic reactor
US7871579B2 (en) Tubular reactor with expandable insert
AU766169B2 (en) Improved scallop design for radial flow reactor internals
CN101896260B (en) Support system for heat exchanger plates in isothermal chemical reactors
US7794676B2 (en) Reactor for a catalytic conversion reaction
KR20100101158A (en) Catalytic reactor
KR20140001590U (en) Heat exchange reactor
WO2003031050A1 (en) Heat exchange reactor
EP2933016A1 (en) Isothermal tubular catalytic reactor
EP2244821B1 (en) Isothermal chemical reactor with plate heat exchanger
JP2012521960A (en) Steam reformer with passive heat flux control element
GB2057908A (en) Fluid-solid contact
EP4532095B1 (en) Catalyst support system for ammonia oxidation burners
US12109561B2 (en) Support structure for structured catalyst packings
EP0792189A1 (en) Catalytic reactor designed to reduce catalyst slumping and crushing
CN223263798U (en) Shell-side structure of shell-and-tube reactor
AU2022227218A1 (en) Heat exchange reactor seal apparatus
WO2022008219A1 (en) Catalytic reactor comprising an expandable structured packing
WO2001037982A1 (en) Steam reforming apparatus

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KN KP KR KZ LC LK LR LS LT LU LV LY MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU LV MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DPE2 Request for preliminary examination filed before expiration of 19th month from priority date (pct application filed from 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2005818933

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 11792289

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: MX/a/2007/006887

Country of ref document: MX

WWE Wipo information: entry into national phase

Ref document number: 1020077013166

Country of ref document: KR

WWE Wipo information: entry into national phase

Ref document number: 2590411

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 2005315872

Country of ref document: AU

Ref document number: 2007545913

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 200580043458.4

Country of ref document: CN

Ref document number: 2623/CHENP/2007

Country of ref document: IN

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2005315872

Country of ref document: AU

Date of ref document: 20051212

Kind code of ref document: A

WWP Wipo information: published in national office

Ref document number: 2005315872

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2007126962

Country of ref document: RU

WWP Wipo information: published in national office

Ref document number: 2005818933

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 11792289

Country of ref document: US