US 20050119109 A1
A cleaning kit for removing process impurities carried on the surface of a NO.sub.x reduction catalyst which is installed in the path of a flue gas flow exiting from a fossil fuel burning facility including: a reagent supply grill; a source of supply of liquid cleaning reagent; a reagent collection basin; and a recirculating structure. The reagent supply grid is adapted to be selectively positioned above a portion of a catalyst layer. The source of supply of liquid cleaning reagent adapted to be in communication with the supply grid, and the reagent collection basin being adapted to be selectively positioned below the portion of such catalyst layer to catch cleaning reagent therein after such reagent passes through such portion of the catalyst layer, the recirculating structure recirculates at least a portion of such reagent from the collecting basin for recirculating through such supply grid for further cleaning of such portion of the catalyst layer.
14. A method for treating wholly or partially deactivated catalytic devices used for nitrogen removal of stack gases, comprising the steps of:
treating the surface of the catalytic devices with a regenerating fluid to remove contaminants from the surface of the catalytic devices without removing the catalytic devices from their normal operating position;
collecting the regenerating fluid and the contaminants;
separating at least a portion of the contaminants from the regenerating fluid;
recirculating the regenerating fluid for reuse in the treatment until the catalytic devices have been regenerated; and,
drying the catalytic devices.
15. The method of
16. The method of
17. A catalyst regeneration system for regenerating deactivated catalytic devices used for nitrogen removal of stack gasses without moving the catalytic devices from its normal operating position, comprising:
a container for storing a regeneration fluid;
a fluid pump for conveying the regeneration fluid to the deactivated catalytic devices;
a treatment system for scrubbing the deactivated catalytic devices with the regeneration fluid to remove contaminates from the deactivated catalytic devices;
a catching system for collecting the runoff of the regeneration fluid and the contaminants;
a waste pump for conveying the regeneration fluid and the contaminates to a separating system;
a separating system for separating the regeneration fluid from at least a portion of the contaminates;
a contaminate transfer system for conveying the contaminates to a treatment area; and,
a recycling pump for conveying the regeneration fluid in the separating system to the container for reuse in the catalyst regeneration system.
18. The catalyst regeneration system of
19. The catalyst regeneration system of
20. The catalyst regeneration system of
21. A cleaning system to remove contaminants carried on a surface of a wholly or partially deactivated NOX reduction catalyst which is installed in a flue gas flow path of a fossil fuel burning facility, comprising:
a movable cleaning reagent supply grid adapted to be selectively positioned above a catalyst layer;
a supply source of liquid cleaning reagent adapted for communication with the supply grid, from which a portion of the liquid cleaning reagent is directed through the supply grid so that essentially all of the catalyst layer is contacted by cleaning reagent, the liquid cleaning reagent removing at least a portion of the contaminants from the catalyst layer;
a cleaning reagent collection basin adapted to be selectively positioned below the catalyst layer to catch cleaning reagent after the reagent passes through the catalyst layer; and
a separating device for removing at least a portion of accumulated solids from the at least a portion of such cleaning reagent prior to recirculation through the supply grid.
22. The cleaning system of
23. The cleaning system of
24. The cleaning system of
The invention relates to a method for scrubbing and/or regenerating of wholly or partially deactivated catalytic devices for nitrogen removal from stack gases, wherein the catalytic devices are treated with a scrubbing, or respectively regeneration fluid.
Such catalytic devices are also called SCR (selective catalytic reduction) catalytic devices. The deactivation of such catalytic devices has several different causes, mainly:
Clogging of the honeycomb structure, or respectively the free spaces in the catalytic device. Because of this, the stack gas does not reach the catalytic device and the clogged conduit of the catalytic device is not used for the catalytic reaction. In order to use the installed catalytic material as efficiently as possible, attempts are made to decrease the clogging of honeycomb channels or plate channels by cleaning measures, such as steam blowers in the DENOX installation or manual cleaning actions. In spite of this, some of these honeycombs, or respectively free spaces in the catalytic device, become clogged over time. With some installations the catalyst modules are removed and placed on an appropriate shaking device. The clogs are loosened by the shaking movements. In this way the stack gas again gains access to the catalytic material. The increase in activity does not constitute a regeneration, it only provides access to the clogged catalytic material. The surface layer being formed during operation remains untouched by this cleaning step.
Worsening of the gas diffusion at the surface of the wall of the catalytic device because of the growth of a thin surface layer of approximately 1 to 100 μm and clogging of pores. Because of this, the stack gas can only reach the pores of the catalytic material poorly or not at all. The formation of a thin surface layer worsens the chemical transformation of NOx and NH3 into N2 and H2O, because the gas diffusion into the catalytic material is greatly hampered.
Clogging of the active catalytic centers on the surface of the catalytic devices by means of the accumulation of the so-called catalytic poisons, for example As, K, Na. The settling of catalytic poisons, such as arsenic, for example, on the active centers of the catalytic device makes the reaction at these centers impossible and in this way also aids in a reduction of the activities of the catalytic material.
Abrasion of catalytic material by solids, such as fly ash, contained in the stack gas. The catalytic material is reduced because of the loss of catalytic material and therefore of the surface available for the reaction. The abrasion of catalytic material is an irreversible process which results in a permanent loss of activity. The following actions can also simultaneously occur in the course of abrasion by fly ash:
A method is described in DE 38 16 600 C2 in which the regeneration of catalytic devices contaminated by arsenic is described. This method does not take into consideration the portion of the deactivation by a gas diffusion-hindering surface layer. Aqueous solutions of nitric acid, hydrochloric acid, sulfuric acid or acetic acid are employed as the scrubbing suspension in the method according to DE 38 16 600 C2. These scrubbing suspensions have the disadvantage that for one they are too expensive and also that the disposal of the acids contaminated by arsenic is elaborate.
A method is described in EP 0 136 966 B1, in which initially the dust adhering to the surface is removed with dry steam. The catalytic poisons are then intended to be dissolved and rinsed out in a second step by wet steam with a moisture content of ≦=0.4. Drying is performed with dry steam again. In the method in accordance with EP 0 136 966 B1, the thin, gas diffusion-hindering layer is not removed in a first step, instead clogged conduits are merely opened again. This has already been done on a large-scale basis for a long time in the form of so-called dust or soot blowers. The second step of this method can have an activity-increasing effect only with catalytic devices wherein the gas diffusion-hindering layer does not exist over the entire surface or not at all. Also, the generation of large amounts of dry and wet steam is very energy-intensive.
A method for the reactivation of catalytic devices is described in DE 30 20 698 C2, which removes the deactivating substances by means of a defined pressure and a defined temperature. Various gases, for example methane, propane, carbon dioxide or argon can be added in the process for optimizing the method. This method also does not consider the gas diffusion-hindering surface layer.
A great disadvantage of most of the mentioned methods is the fact that they can only be performed in a separate installation. To this end the removal of the catalytic devices and therefore an outage of the installation is required.
Accordingly, it is the object of the invention to further develop a method of the type mentioned above in such a way that gas diffusion on the surface of the catalytic devices is again made possible, wherein additionally the clogging of the active centers by catalytic poisons is reversed to the greatest extent possible, and which can be performed inside the nitrogen removal installation without the removal of the catalytic devices.
This object is attained in that the scrubbing, or respectively regenerating fluid is fully desalinated water.
The function of the invention is based on the dissolution and removal of the surface layer for restoring the gas diffusion and exposing of active centers for the nitrogen-removing reaction of the surface of the catalytic device. In this case the composition of the fluid must be selected in such a way that, along with a small consumption of regenerating suspension, the fastest possible dissolution of the surface layer is achieved. In connection with the regeneration of SCR catalytic devices it has surprisingly been shown to be useful to employ fully desalinated water, for example demineralized water, for dissolving the surface layer. The use of demineralized water as the scrubbing fluid prevents the introduction of catalytic poisons with the scrubbing fluid. In comparison with other possible fluids, demineralized water has the advantage that it is relatively inexpensive and that in most cases it can be produced at the location of the power plant itself. The cleaning and regeneration of the catalytic devices is performed at ambient temperatures, so that no energy is required for heating the fluid. By means of this method it is possible to drastically reduce the number of deactivated catalytic devices to be disposed. Above all, in large installations for the reduction of nitric oxides, so-called DENOX installations, this method is suitable for regenerating the used and deactivated catalytic devices, i.e. to again increase the reduced catalytic activities, without having to remove them.
An advantageous further development of this method provides, that the catalytic devices are first mechanically cleaned by vacuuming or blowing the deposits out, which is then followed by a scrubbing cycle, which removes the surface layer by means of a regenerating suspension and dissolves the clogs of the active centers to a great extent. It has been shown to be advantageous for the consumption of regenerating suspension if only a small portion of the regenerating suspension is continuously removed and regenerated, i.e. the larger part can be employed in a recirculating operation.
An additional opportunity for reducing the scrubbing water is the use of a suitable abrasive which only removes the surface layer. This method can also be practiced inside the nitrogen removal installation. The abrasive (for example small glass spheres), together with the parts of the gas diffusion-hindering surface layer, can then be disposed of together with the fly ash from the electronic filter.
Further advantageous developments of the invention are defined in the dependent claims.
An exemplary embodiment for the use of a suitable regeneration device will be described in greater detail in what follows, making reference to the attached drawings. Represented are in:
An exemplary embodiment of the present invention becomes clear by means of the flow graph of the method represented in
A container 11 is filled with desalted water, for example demineralized water, from the complete desalination installation of a power plant, via a line 1. Additives can be supplied to the scrubbing fluid via lines 2 and 3, for example hydrochloric acid for lowering the pH value, or regenerating substances, such as vanadium, molybdenum or tungsten, for example. The pump 4 conveys the regenerating suspension through the line 5 into the DENOX installation 17, where the catalytic devices 6 are scrubbed. The scrubbing fluid with the materials contained in the surface layer and the catalytic poisons are conducted via a suitable catching device, for example a funnel, and a pump 7 to a separating device 8. There, the materials contained are separated in a suitable manner from the scrubbing fluid. A hydrocyclone, for example, is suitable for this. However, filters or the like are also conceivable. The underflow from the separating device 8, which is heavily loaded with solids, is conveyed via the pump 16 to a settling tank 9. The solid components are further concentrated in this settling tank 9, are drawn off in a partial flow via a line 10, and conveyed to a suitable waste water treatment, not represented here. The overflow of the settling tank 9 and the upper flow of the separating device 8 are conveyed to the container 11 via the lines 12 and 13 and pumps 14 and 15.
This structure can be expanded by suitable precipitation stages, in which dissolved noxious matter, such as the catalytic poison arsenic, for example, is precipitated, so that it can be separated by means of the separating device 8 and removed from the scrubbing fluid. The scrubbing, or respectively regenerating fluid is conveyed in circulation in this way, from which only a defined volume of fluid with the concentrated noxious matter, is removed per circuit. This volume is replenished through the lines 1, 2 and 3.
A further possibility for execution is closing the honeycombs of the catalytic device, or respectively of the reactor, below the catalytic device 6. The catalytic devices are thereafter filled with the scrubbing, or respectively regenerating fluid. During this bath in the regenerating fluid, first the gas diffusion-hindering surface layer is loosened. The catalytic poisons inside the pores of the catalytic device are then loosened from the active centers on the surface of the catalytic device and are transferred into the regenerating fluid. Because of the concentration drop between the regenerating fluid inside the pores of the catalytic device and the regenerating fluid in the honeycomb channels, the dissolved catalytic poisons move to the honeycomb channels. After a defined period of time the regenerating fluid with the components of the gas diffusion-hindering surface layer and the catalytic poisons is drained. The catalytic devices are thereafter dried by means of stack gas or hot air. The advantage of this embodiment lies in the low consumption of regenerating fluid.
Complementing the mentioned exemplary embodiments it is also possible to connect the regeneration of catalytic devices directly with drying. In large nitrogen-removing installations it can occur that some tons of regenerating fluid still remain in the catalytic devices 6. The structural steel for receiving the catalytic modules must be designed for this additional weight. This is not the case in some installations. It is then necessary to dry a partial section immediately after the regeneration of this section. In the course of this, the catalytic devices 6 are first regenerated as described. Following regeneration, the regenerated section is dried by means of hot air or hot gas. By means of this the regenerating suspension remaining in the catalytic devices 6 is evaporated and removed.
The invention was tested on used and deactivated catalytic devices. To this end, a deactivated catalytic element of a total length of 840 mm and edges of the length of 150×150 mm was removed from a DENOX installation and treated in accordance with the regenerating method. Prior to regeneration with demineralized water, the catalytic element was examined in a test stand. The catalytic element was thereafter rinsed for 5 minutes with demineralized water and subsequently dried with hot air. A subsequent examination showed that the NOX precipitation rate was increased by approximately 5% to 6% over the entire mol ratio range of NH2/NOX of 0.8 to 1.2, as shown in the following table.