Thin layer fixed bed reactor for the chemical treatment of a finely divided catalytic solid

US9050569B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9050569-B2
Application numberUS-68227708-A
CountryUS
Kind codeB2
Filing dateSep 15, 2008
Priority dateOct 10, 2007
Publication dateJun 9, 2015
Grant dateJun 9, 2015

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention describes a thin layer fixed bed reactor intended for chemical treatments, in particular reduction of a Fischer-Tropsch synthesis catalyst. The reactor is designed in the form of similar, compact modules and operates with a ratio of linear pressure drop to outlet pressure which falls within certain limits.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for operating a fixed bed reactor with thin layers having a thickness in the range 10 to 500 mm, intended for the treatment of solid particles with a size in the range 30 to 100 microns, said reactor comprising: a plurality of similar modules (M) operating in parallel, enclosed in a common vessel (R) of said reactor, wherein each module (M) comprises: at least two thin layers (CM), having a thickness in the range 10 to 500 mm, of solid particles, with a size in the range 30 to 100 microns, wherein each thin layer is enclosed by a partially porous envelope (P) partially porous envelope (P) having a porous inlet face and a porous outlet face; each of the porous inlet faces of the partially porous envelopes is coupled with at least one diffuser (D) for introduction of reagent gas, wherein diffusers between two adjacent modules are coupled to a porous inlet face of a partially porous envelope in each of said two adjacent modules; each of the porous outlet faces of the partially porous envelopes is coupled with at least one collector (CL) for removal of effluents; at least one pipe (E) for admitting reagent gas into said at least one diffuser (D), wherein said at least one pipe (E) for admitting reagent gas communicates with the exterior of the reactor; at least one pipe (C) for recovering reaction effluents, wherein said at least one pipe (C) for recovering reaction effluents communicates with the exterior of the reactor; at least one pipe (S) for admitting solid particles to be treated into the partially porous envelopes (P); at least one pipe (V) for evacuating treated solid particles from the partially porous envelopes (P), distinct from said at least one pipe (S) for admitting solid particles; said plurality of modules (M) being arranged inside said common vessel (R) so as to form an assembly with a planar or cylindrical geometry; said method comprising the following phases in succession: phase 1: charging solid particles to be treated into upstream metering devices (D am ) and flushing with an inert gas; phase 2: charging solid particles into at least one of said plurality of modules via said at least one pipe (S) for admitting solid particles; phase 3: flushing the charged module or modules with an inert gas; phase 4: treating the charged module or modules with H 2 diluted with nitrogen, at a fixed pressure, and following a temperature ramp-up rate in the range 0.5° C. to 5° C./minute; phase 5: treating the charged module or modules in H 2 , at fixed temperature and pressure, for a fixed period (stages of 4 to 20 hours); phase 6: flushing the charged module or modules after treatment using an inert gas; phase 7: discharging solid particles from the charged module or modules using said at least one pipe (V) for evacuating treated solid particles to downstream metering devices (Dav); phase 8: cooling treated solid particles to a temperature in the range 100° C. to 150° C.; and phase 9: transferring cooled solid particles; a) directly to a Fischer-Tropsch synthesis reactor; b) to a mixer (M j ) wherein the cooled solid particles are mixed with paraffin waxes having a melting point of close to 100° C. with a flush of inert gas, and transferring solid particles which have been coated with waxes into barrels (Bs); or to an intermediate capacity, and optionally transferring solid particles into barrels (Bs). 2. The method according to claim 1 , in which the number of modules (M) in the fixed bed reactor is in the range of 4 to 12. 3. The method according to claim 1 , in which, for each thin layer (CM), the ratio of the linear pressure drop across the thin layer (DP/z) over the pressure at the outlet from said thin layer (Ps) is in the range of 0.5 m −1 to 5 m −1 . 4. The method according to claim 1 , in which said partially porous envelope (P) is constituted by a screen with a planar form having a mesh with a dimension in the range of 5 to 10 microns. 5. The method according to claim 1 , wherein said solid particles are catalyst particles used for Fischer-Tropsch synthesis, and the hourly space velocity is in the range of 1.5 to 3 Nliters/h of H 2 per gram of catalyst. 6. The method according to claim 1 , wherein said solid particles are catalyst particles used for Fischer-Tropsch synthesis, and the maximum temperature in phase 5 is in the range of 350° C. to 400° C. 7. The method according to claim 1 , wherein each of said thin layers has an annular form. 8. The method according to claim 1 , wherein each of said thin layers has a parallelepipedal form. 9. The method according to claim 1 , wherein said solid particles are catalyst particles used for Fischer-Tropsch synthesis, and for each thin layer (CM), the ratio of the linear pressure drop across the thin layer (DP/z) over the pressure at the outlet from said thin layer (Ps) is in the range 0.1 m −1 to 10 m −1 . 10. The method according to claim 2 , wherein for each thin layer (CM), the ratio of the linear pressure drop across the thin layer (DP/z) over the pressure at the outlet from said thin layer (Ps) is in the range of 0.5 m −1 to 5 m −1 . 11. The method according to claim 1 , wherein the quantity of solid particles contained in each module (M) is in the range 50 to 1000 kg. 12. The method according to claim 1 , wherein said at least one pipe (E) for admission of reagent gas, said at least one pipe (S) for admission of solid particles to be treated, and said at least one pipe (C) for collecting effluents are disposed on an upper flange of said reactor which closes an upper portion of said reactor. 13. The method according to claim 1 , wherein each module (M) has a planar geometry, with a height in the range 0.5 to 4 m, a width in the range 0.5 to 4 m, and a thickness of the thin layer of solid particles to be treated in the range 50 mm to 300 mm. 14. The method according to claim 13 , wherein each module (M) has a thickness of the thin layer of solid particles to be treated in the range of 100 mm to 200 mm. 15. The method according to claim 1 , wherein the number of modules (M) in the reactor is in the range 2 to 20. 16. The method according to claim 1 , wherein, for each thin layer (CM), the ratio of the linear pressure drop across the thin layer (DP/z) over the pressure at the outlet from said thin layer (Ps) is in the range 0.1 m −1 to 10 m −1 . 17. The method according to claim 1 , wherein the quantity of solid particles to be treated per module of the reactor is in the range 100 to 500 kg. 18. The method according to claim 1 , wherein said partially porous envelope (P) is constituted by a screen with a planar form having a mesh with a dimension in the range 1 to 20 microns. 19. The method according to claim 1 , wherein said solid particles are catalyst particles used for Fischer-Tropsch synthesis, and the hourly space velocity is in the range 0.5 to 5 Nliters/h of H 2 per gram of catalyst. 20. The method according to claim 1 , wherein said solid particles are catalyst particles used for Fischer-Tropsch synthesis, and the maximum temperature in phase 5 is in the range 300° C. to 450° C. 21. The method according to claim 1 , wherein said solid particles are catalyst particles used for Fischer-Tropsch synthesis, and the ramp-up followed for the reactor temperature rise is in the range 1° C. to 5° C./minute. 22. The method according to claim 1 , wherein said solid particles are catalyst particles based on a noble metal employed for reforming oil cuts with a

Assignees

Inventors

Classifications

  • characterised by dimensions, e.g. grain size (in a colloidal state B01J35/23; crystallite size B01J35/77) · CPC title

  • B01J8/009Primary

    Membranes, e.g. feeding or removing reactants or products to or from the catalyst bed through a membrane · CPC title

  • Feeding reactive fluids (for solid material B01J8/0015) · CPC title

  • in a cylindrical annular shaped bed · CPC title

  • Feeding reactive fluids · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9050569B2 cover?
The present invention describes a thin layer fixed bed reactor intended for chemical treatments, in particular reduction of a Fischer-Tropsch synthesis catalyst. The reactor is designed in the form of similar, compact modules and operates with a ratio of linear pressure drop to outlet pressure which falls within certain limits.
Who is the assignee on this patent?
Douziech Damien, Causse Gilles, Caprani Eric, and 5 more
What technology area does this patent fall under?
Primary CPC classification B01J8/009. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Jun 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).