Method and reactor for performing exothermic reactions
11065591 · 2021-07-20
Assignee
Inventors
- Christian Henrik Speth (Lynge, DK)
- Tommy Lykke Wind (Allerød, DK)
- Uffe Bach Thomsen (Vedbæk, DK)
- Anders Helbo HANSEN (Espergærde, DK)
Cpc classification
C01C1/0417
CHEMISTRY; METALLURGY
B01J8/0469
PERFORMING OPERATIONS; TRANSPORTING
Y02P20/52
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
C01B2203/0283
CHEMISTRY; METALLURGY
B01J2208/021
PERFORMING OPERATIONS; TRANSPORTING
B01J8/0496
PERFORMING OPERATIONS; TRANSPORTING
International classification
B01J8/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A method and reactor for performing exothermic reactions with parallel operated catalyst modules arranged in stacked order within a pressure shell and adapted to axial flow of process gas through one or more catalyst layers and at least one catalyst layer cooled by an intrabed heat exchanger.
Claims
1. Method of performing exothermic catalytic reactions comprising the steps of: passing a fresh process gas in parallel to at least two cylindrical catalyst modules arranged in stacked order, each containing in series one or more catalyst zones, at least one of the catalyst zones is cooled by an intrabed heat exchanger; exothermically reacting the fresh process gas flowing in axial flow direction through all of the catalyst zones to a product gas; in each of the cylindrical catalyst modules, cooling the exothermic reacting process gas with the fresh process gas and thereby preheating the fresh process gas by passing the fresh process gas from an outer annular space formed around each of the cylindrical catalyst modules into the intrabed heat exchanger and passing the fresh process gas through the intrabed heat exchanger in indirect heat exchange with the exothermic reacting preheated process gas passing in axial flow direction through the cooled catalyst zone; and collecting the product gas withdrawn from the at least two catalyst modules in a central space formed centrally within the at least two stacked catalyst modules.
2. The method of claim 1, wherein at least one of serial connected catalyst zones is an adiabatic catalyst zone.
3. The method of claim 1, wherein the process gas from a single cooled catalyst zone is passed in series through a single adiabatic catalyst zone.
4. The method of claim 1, wherein the intrabed bed heat exchanger comprises a plurality of cooling plates forming flow compartments for the fresh process gas in the intrabed heat exchanger.
5. The method of claim 4, wherein the thickness of the cooled catalyst layer between two adjacent cooling plates varies within ±10%.
6. The method of claim 5, wherein the thickness of the cooled catalyst layer between two adjacent cooling plates is between 10 and 300 mm.
7. The method of claim 6, wherein the thickness of the cooled catalyst layer between two adjacent cooling plates is between 20 and 150 mm.
8. The method of claim 5, wherein each of the cooling plate is essentially planar.
9. The method of claim 5, wherein the cooling plates are arranged in three 120° sections in the cylindrical catalyst modules and wherein all cooling plates in each 120° section are essentially planar and parallel.
10. The method of claim 9, wherein the essentially planar and parallel cooling plates in any of the three 120° sections are non-parallel to the essentially planar and parallel cooling plates in another section.
11. The method of claim 1, wherein the fresh process gas is passed through the intra bed heat exchanger in counter-current flow or in co-current flow with the process gas passing through the catalyst zones in each of the cylindrical catalyst modules.
12. The method of claim 1, wherein the fresh process gas is passed through the intrabed heat exchanger in counter-current flow with the process gas passing through the catalyst zones in each of the cylindrical catalyst modules.
13. The method of claim 1, wherein the cylindrical catalyst modules have the same size.
14. A reactor for performing exothermic reactions, comprising within a cylindrical pressure shell: at least two parallel operated cylindrical catalyst modules arranged in stacked order, each containing in series one or more catalyst zones with a catalyst layer adapted to axial flow, the catalyst layer in the at least one of the catalyst zones is cooled by an intrabed heat exchanger; an outer annular space between the cylindrical catalyst modules and the cylindrical pressure shell fluidly connected to the at least two parallel cylindrical catalyst modules; in the at least one cooled catalyst zone feed means for the fresh process gas into the inlet of the intrabed heat exchanger, fluidly connected to the outer annular space; the outlet of the intrabed heat exchanger is formed by open ends of the intrabed heat exchanger in the at least one cooled catalyst zone; covers closing the at least two parallel cylindrical catalyst modules; and outlet means from the at least two parallel cylindrical catalyst modules.
15. The reactor of claim 14, wherein the outlet means from the at least two parallel cylindrical catalyst modules is arranged in a central space formed centrally within the at least two stacked catalyst modules.
16. The reactor of claim 14, wherein at least one of the serial catalyst zones is an adiabatic catalyst zone.
17. The reactor of claim 14, having a single cooled catalyst zone connected in series with a single adiabatic zone.
18. The reactor of claim 14, wherein the intrabed bed heat exchanger is a plate heat exchanger with a plurality of cooling plates forming flow compartments for fresh process gas in the intrabed heat exchanger.
19. The reactor of claim 17, wherein the thickness of the cooled catalyst layer between two adjacent cooling plates varies within ±10%.
20. The reactor of claim 19, wherein the thickness of the cooled catalyst layer between two adjacent cooling plates is between 10 and 300 mm.
21. The reactor of claim 19, wherein the thickness of the cooled catalyst layer between two adjacent cooling plates is between 20 and 150 mm.
22. The reactor of claim 18, wherein each of the cooling plates is essentially planar.
23. The reactor of claim 18, wherein the cooling plates are arranged in three 120° sections in the cylindrical catalyst modules and wherein all cooling plates in each 120° section are essentially planar and parallel.
24. The reactor of claim 23, wherein the essentially planar and parallel cooling plates in any of the three 120° sections are non-parallel to the essentially planar and parallel cooling plates in another section.
25. The reactor of claim 14, wherein the cylindrical catalyst modules have the same size.
26. The reactor of claim 18, wherein the cooling plates are in the form of pillow plates.
27. The reactor of claim 14, wherein the inlet to the intrabed heat exchanger is provided with gas feed means fluidly connected to the outer annular space.
28. The reactor of claim 14, wherein the outlet means from the lower most catalyst zone in each of the at least two parallel operated cylindrical catalyst modules are fluidly connected to a space formed centrally within the at least two stacked catalyst modules.
29. The reactor of claim 14, wherein the reactor contains additional inlet means for supply of a further stream of preheated process gas.
30. The reactor of claim 29, wherein the means for supply of the further stream of preheated process gas is arranged to bypass the outer annular space and the intrabed heat exchanger.
31. The reactor of claim 14, wherein the reactor contains means for supply of a further stream of fresh process gas.
32. The reactor of claim 30, wherein the means for supply of the further stream of fresh process gas is arranged to bypass the outer annular space and the intrabed heat exchanger.
Description
DESCRIPTION OF THE FIGURES
(1)
(2)
(3)
(4)
(5)
(6)
(7)
DETAILED DESCRIPTION OF THE INVENTION
(8) The invention describes a method of performing exothermic catalytic reactions wherein fresh process gas is passed in parallel to at least two cylindrical catalyst modules arranged in stacked order.
(9)
(10) The invention is not limited to the above examples of heat exchange units depicted in
(11)
(12)
(13)
(14)
(15) Finally,
Example
(16) An investigation of the proposed concept of the invention was made for ammonia synthesis application with reference to the present ‘state of the art’ being a radial flow converter since it is presently the preferred choice for large scale ammonia plants. In detail, the methods of the invention were compared to a three bed radial flow converter having two interbed heat exchangers for preheating of fresh process gas and for cooling in-between the catalyst beds.
(17) The converter, according to the invention, was equipped with a number of parallel operated cylindrical catalyst modules adjusted to give a total converter pressure drop below 1 kg/cm2. Each catalyst module consisted of a cooled catalyst zone, holding an intrabed heat exchanger, connected in series with an adiabatic catalyst zone. Axial flow through both catalyst zones of each catalyst module was utilized. The intrabed heat exchanger of each catalyst module consisted of parallel cooling plates proving constant catalyst layer thickness in the cooled catalyst zone. The size of the pressure shell, applied for the two converter types, was the same. Moreover, the loop pressure applied was equal and the same ammonia catalyst was considered in both cases.
(18) The main results are listed in the below Table.
(19) TABLE-US-00001 TABLE Converter type ′State of the art′ Converter radial flow according to Parameter converter the invention Additional catalyst — 24% loading volume Improvement of — 4.5% specific catalyst production rate Additional converter — 30% capacity (production rate) Pressure drop reduction — 64% Reduction of maximum — 75% catalyst zone height Reduction of catalyst — 53% bed weight
(20) The investigation shows that the methods of the present invention provide a number of value propositions compared to the prior art:
(21) Better utilization of the available pressure shell volume is obtained and 24% more catalyst can be loaded into an identical pressure shell.
(22) The specific catalyst production rate, in metric tons of ammonia produced per day per catalyst volume is improved by 4.5%, achieved by the parallel placed cooling plates in the cylindrical modules providing constant catalyst layer thickness and improved reaction conditions for the catalyst of the cooled catalyst zone.
(23) The synergetic effect of the above two points ensures the ability to produce 30% extra ammonia within a fixed pressure shell. This is a significant achievement of value in both revamp scenarios as well as for grass root plants. Associated savings on investment cost will follow for the pressure shell.
(24) The pressure drop over the converter was in the present investigation lowered by no less than 64% giving reduced operation costs and improved energy efficiency.
(25) The maximum catalyst zone height was reduced by 75% providing significantly reduced catalyst forces on the mechanical parts and reduced risk of failures.
(26) The catalyst bed weight was lowered by 53% obtained by the concept of catalyst modules operating in parallel. This eases the possibility of loading catalyst on ground, and installing the catalyst and hardware (modules) simultaneously by lifting the pre-loaded modules directly into the pressure shell for reduced installation time.