DEVICE SYSTEM AND METHOD HAVING SINTERING FLUE GAS CO CATALYTIC HEAT EXCHANGE AND MEDIUM-AND-LOW-TEMPERATURE SCR DENITRATION CONNECTED IN SERIES

Abstract

Disclosed in the present invention are a device system and method having sintering flue gas CO catalytic heat exchange and medium-and-low-temperature SCR denitration connected in series. In the device system, a CO catalytic heat storage and exchange device is arranged to completely replace an original heat exchanger arranged after a raw desulfurized flue gas pipe. The method comprises respectively carrying out first CO catalytic conversion and second CO catalytic conversion on sintering flue gas and denitrated flue gas by means of the CO catalytic heat storage and exchange device, thereby increasing CO conversion efficiency and reducing overall resistance of the system. In addition, the present invention takes both CO pollution control and carbon emission reduction into consideration and thus has good economic benefits and a good application prospect.

Claims

1. A method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, which is performed with a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration; the device system comprises a CO catalytic regenerative heat exchange device, an ammonia spray device, and a medium/low-temperature SCR denitration reaction device which are sequentially connected along the flow direction of raw flue gas; a sintering flue gas inlet of the CO catalytic regenerative heat exchange device is directly connected to a desulfurized raw flue gas pipeline; a purified flue gas outlet of the medium/low-temperature SCR denitration reaction device is connected to a denitrated flue gas inlet of the CO catalytic regenerative heat exchange device; a CO heat-regenerative catalyst comprises a cordierite honeycomb ceramic heat-regenerative framework and an active component which is arranged on the cordierite honeycomb ceramic heat-regenerative framework the cordierite honeycomb ceramic heat-regenerative framework has a porosity of 0.5-0.7; the method comprises the following steps: (1) subjecting sintering flue gas to the CO catalytic regenerative heat exchange device to perform a first CO catalytic conversion and heat the sintering flue gas to obtain heated flue gas; (2) mixing the heated flue gas with an ammonia source by the ammonia spray device, and then introducing into the medium/low-temperature SCR denitration reaction device to perform an SCR denitration reaction to obtain denitrated flue gas; a temperature of the heated flue gas which is introduced into the ammonia spray device in step (2) is 220-280 C., and a complete reaction temperature of the CO heat-regenerative catalyst in the CO catalytic regenerative heat exchange device is 180-220 C.; and (3) introducing the denitrated flue gas into the CO catalytic regenerative heat exchange device to perform heat exchange cooling and a second CO catalytic conversion to obtain purified sintering flue gas; using heat release from CO catalytic oxidation to replace heat compensation of hot blast furnace fuel and a heat exchanger device; for the flue gas with a flow rate of 850000 Nm.sup.3/h, the total system pressure drop is less than or equal to 1900 Pa; the consumption of blast furnace gas is less than or equal to 50000 m.sup.3 in 30 days; the NO.sub.x concentration in the purified flue gas is less than or equal to 40 mg/m.sup.3, and the CO concentration in the purified flue gas is less than or equal to 500 mg/m.sup.3.

2. The method according to claim 1, wherein the CO catalytic regenerative heat exchange device comprises a heat exchange device shell, and the CO heat-regenerative catalyst and a heat exchange element which are provided inside the heat exchange device shell; a guide bearing inside a central axis of the CO catalytic regenerative heat exchange device, and the CO heat-regenerative catalyst and the heat exchange element are allowed to rotate around the guide bearing.

3. The method according to claim 2, wherein the heat exchange element is arranged lower than the CO heat-regenerative catalyst.

4. (canceled)

5. The method according to claim 1, wherein an SCR denitration catalyst is arranged in the medium/low-temperature SCR denitration reaction device.

6.-8. (canceled)

9. The method according to claim 1, wherein at the stage where the process of step (1) is being started up, the heated flue gas is subjected a hot blast furnace device for heat compensation before introduced to the ammonia spray device.

10. The method according to claim 1, wherein a CO concentration in the sintering flue gas is 6000-12000 mg/Nm.sup.3.

11. (canceled)

12. The method according to claim 1, wherein a catalyst for the SCR denitration reaction in step (2) comprises a vanadium-tungsten-titanium catalyst and/or a vanadium-molybdenum-titanium catalyst.

13. (canceled)

14. The method according to claim 10, wherein the CO concentration in the sintering flue gas is 8000-12000 mg/Nm.sup.3.

15. The method according to claim 1, wherein a catalyst for the SCR denitration reaction in step (2) is V.sub.2O.sub.5WO.sub.3/TiO.sub.2 and/or V.sub.2O.sub.5MoO.sub.3/TiO.sub.2.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0056] The accompanying drawings are used to provide a further understanding of the technical solutions herein, and form a part of the specification, which are used together with embodiments of the present application to explain the technical solutions herein, and do not constitute a limitation on the technical solutions herein.

[0057] FIG. 1 is a drawing showing a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration provided by specific embodiments.

[0058] FIG. 2 is a detailed drawing showing the CO catalytic regenerative device in FIG. 1.

[0059] Reference list: 1CO catalytic regenerative heat exchange device; 2hot blast furnace device; 3ammonia spray device; 4low/medium-temperature SCR denitration reaction device; 5shell; 6CO heat-regenerative catalyst; 7heat exchange element; and 8guide bearing.

DETAILED DESCRIPTION

[0060] The technical solutions of the present application are further explained with reference to the accompanying drawings and embodiments.

[0061] The present application is described in further detail below. However, the following examples are only simple examples of the present application and do not represent or limit the protection scope of the present application, and the protection scope of the present application is subject to the claims.

[0062] It should be understood that in the description of the present application, the orientation or position relationship indicated by the terms, such as center, longitudinal, lateral, up, down, front, back, left, right, vertical, horizontal, top, bottom, inside, outside, etc., is based on the orientation or position relationship shown in the drawings, which is only intended to facilitate the description of the present application and to simplify the description, but not to indicate or imply that the device or element referred to must have a particular orientation or must be constructed and operated in a specific orientation, and therefore cannot be regarded as a limitation of the present application. In addition, terms such as first and second are used only for descriptive purposes and cannot be understood as indicating or implying relative importance or implicitly specifying the number of technical features referred to. Thus, features defined by first and second can explicitly or implicitly comprise one or more of the features. In the description of the present application, unless otherwise stated, a plurality of means two or more.

[0063] It should be noted that in the description of the present application, unless otherwise specified or limited, the terms such as arrange, attach, and connect are to be understood in a broad sense, for example, as a fixed connection, or as a detachable connection, or as an integrated connection; as a mechanical connection, or as an electrical connection; as a direct connection, or as an indirect connection via an intermediate medium, or as a communication between two elements. For those skilled in the field, the specific meaning of the above terms in the present application can be understood in the light of specific cases.

[0064] Those skilled in the art should understand that in the present application, the necessary pipelines, regular valves, and general pumps required to complete the process are necessarily comprised, but the above contents do not belong to the main application ideas of the present application, and those skilled in the art may add additional arrangements based on the process flow and equipment structure selection, and there are no special requirements or specific restrictions on this aspect in the present application.

[0065] As a specific embodiment of the present application, a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration is provided, as shown in FIG. 1 and FIG. 2. The device system comprises: a CO catalytic regenerative heat exchange device 1, an ammonia spray device 3, and a medium/low-temperature SCR denitration reaction device 4 which are sequentially connected along the flow direction of raw flue gas; a sintering flue gas inlet of the CO catalytic regenerative heat exchange device 1 is directly connected to a desulfurized raw flue gas pipeline; a purified flue gas outlet of the medium/low-temperature SCR denitration reaction device 4 is connected to a denitrated flue gas inlet of the CO catalytic regenerative heat exchange device 1.

[0066] The CO catalytic regenerative heat exchange device 1 comprises a heat exchange device shell 5, and a CO heat-regenerative catalyst 6 and a heat exchange element 7 which are provided inside the heat exchange device shell 5. A guide bearing 8 inside a central axis of the CO catalytic regenerative heat exchange device 1, and the CO heat-regenerative catalyst 6 and the heat exchange element 7 can rotate around the guide bearing 8.

[0067] The CO catalytic regenerative heat exchange device 1 is further provided with a turnplate, the turnplate can rotate around the guide bearing 8, and the CO heat-regenerative catalyst 6 and the heat exchange element 7 are arranged inside the turnplate. When the turnplate rotates around the guide bearing 8, the CO heat-regenerative catalyst 6 and the heat exchanger element 7 can simultaneously rotate with the turnplate around the guide bearing 8 because they are fixed inside the turnplate. The heat exchange element 7 is arranged lower than the CO heat-regenerative catalyst 6.

[0068] The CO heat-regenerative catalyst 6 comprises a cordierite honeycomb ceramic heat-regenerative framework and an active component which is arranged on the cordierite honeycomb ceramic heat-regenerative framework.

[0069] A usage amount of the catalyst and a usage amount of the heat exchange element can be adjusted in a coordinated way, that is, a volume of the CO heat-regenerative catalyst and a heat exchange area of the heat exchange element can be adjusted, the volume of CO heat-regenerative catalyst is about 85-170 m.sup.3, the heat exchange area of the heat exchange element on the raw flue gas side is about 20000-40000 m.sup.2, and the heat exchange area of the heat exchange element on the purified flue gas side is about 30000-60000 m.sup.2 (estimated based on the flow rate of the sintering flue gas of 850000 Nm.sup.3/h).

[0070] A porosity of the cordierite honeycomb ceramic heat-regenerative framework is 0.5-0.7; a size of the catalyst is 90-110 mm90-110 mm30-50 mm; the active component comprises precious metal platinum; the heat exchange element has a corrugated structure; the heat exchange element has a hot-side material of SPCC (cold-reduced carbon steel sheet and strip of commercial qualities), and a cold-side material of enamel or corrosion-resistant steel; a radial sealing sheet and an axial sealing sheet for sequestering the sintering flue gas and the denitrated flue gas from each other are arranged inside the turnplate of the CO catalytic regenerative heat exchange device.

[0071] An SCR denitration catalyst is arranged in the medium/low-temperature SCR denitration reaction device 4.

[0072] A hot blast furnace device 2 is further arranged between the CO catalytic regenerative heat exchange device 1 and the ammonia spray device 3.

[0073] As another specific embodiment of the present application, a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration is provided, and the method comprises the following steps: [0074] (1) sintering flue gas is subjected to a first CO catalytic conversion by the CO catalytic regenerative heat exchange device, and the sintered flue gas is heated to obtain heated flue gas; [0075] (2) the heated flue gas is mixed with an ammonia source by an ammonia spray device, and then introduced into a medium/low-temperature SCR denitration reaction device to perform an SCR denitration reaction to obtain denitrated flue gas; and [0076] (3) the denitrated flue gas is introduced into the CO catalytic regenerative heat exchange device, and subjected to heat exchange cooling and a second CO catalytic conversion to obtain the purified sintering flue gas.

[0077] After a cycle of step (1) to step (3), the CO heat-regenerative catalyst and the heat exchange element that store heat are transferred around the guide bearing to the sintering flue gas side, that is, circling back to step (1), the CO heat-regenerative catalyst and the heat exchange element release heat to raise the temperature of the sintering flue gas.

[0078] When the process of step (1) is being started, the heated flue gas is first compensated in heat by the hot blast furnace device, and then introduced to the ammonia spray device. When the system device is running stably, the heat of the denitrated flue gas is stored in the CO heat-regenerative catalyst and the heat exchange element by the CO catalytic regenerative heat exchange device to transfer to the sintering flue gas, in which case the fuel feed can be stopped, and the hot blast furnace device can be shut down.

[0079] Typical but non-limiting examples of the present application are as follows:

Example 1

[0080] This example provides a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, and the device system comprised: a CO catalytic regenerative heat exchange device, an ammonia spray device, and a medium/low-temperature SCR denitration reaction device which were sequentially connected along the flow direction of raw flue gas; the sintering flue gas inlet of the CO catalytic regenerative heat exchange device was directly connected to the desulfurized raw flue gas pipeline; the purified flue gas outlet of the medium/low-temperature SCR denitration reaction device was connected to the denitrated flue gas inlet of the CO catalytic regenerative heat exchange device.

[0081] The CO catalytic regenerative heat exchange device comprised a heat exchange device shell and a CO heat-regenerative catalyst and a heat exchange element which were provided inside the heat exchange device shell. A guide bearing inside a central axis of the CO catalytic regenerative heat exchange device, and the CO heat-regenerative catalyst and the heat exchange element can rotate around the guide bearing.

[0082] The CO catalytic regenerative heat exchange device was further provided with a turnplate, the turnplate can rotate around the guide bearing, and the CO heat-regenerative catalyst and the heat exchange element were arranged inside the turnplate. When the turnplate rotates around the guide bearing, the CO heat-regenerative catalyst and the heat exchanger element can simultaneously rotate with the turnplate around the guide bearing because they are fixed inside the turnplate. The heat exchange element was arranged lower than the CO heat-regenerative catalyst.

[0083] The CO heat-regenerative catalyst comprised a cordierite honeycomb ceramic heat-regenerative framework and an active component which was arranged on the cordierite honeycomb ceramic heat-regenerative framework.

[0084] A usage amount of the CO heat-regenerative catalyst was 85 m.sup.3, a heat exchange area of the heat exchange element on the raw flue gas side was about 40000 m.sup.2, and a heat exchange area of the heat exchange element on the purified flue gas side was about 60000 m.sup.2 (estimated based on the flow rate of the sintering flue gas of 850000 Nm.sup.3/h).

[0085] A porosity of the cordierite honeycomb ceramic heat-regenerative framework was 0.6; a size of the catalyst was 100 mm100 mm30 mm; the active component comprised precious metal platinum; the heat exchange element had a corrugated structure; the heat exchange element had a hot-side material of SPCC (cold-reduced carbon steel sheet and strip of commercial qualities), and a cold-side material of corrosion-resistant steel; a radial sealing sheet and an axial sealing sheet for sequestering the sintering flue gas and the denitrated flue gas from each other were are arranged inside the turnplate of the CO catalytic regenerative heat exchange device.

[0086] An SCR denitration catalyst was arranged in the medium/low-temperature SCR denitration reaction device.

[0087] A hot blast furnace device was further arranged between the CO catalytic regenerative heat exchange device and the ammonia spray device.

Example 2

[0088] This example provides a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, the structure of the device system refers to the structure in Example 1, and the difference was only that: the hot blast furnace device was arranged before the CO catalytic regenerative heat exchange device, i.e., the sintering flue gas inlet of the hot blast furnace device was connected to the desulfurized raw flue gas pipeline, the raw flue gas outlet of the hot blast furnace device was connected to the sintering flue gas inlet of the CO catalytic regenerative heat exchange device, and the sintering flue gas outlet of the CO catalytic regenerative heat exchange device was connected to the ammonia spray device.

[0089] Example 1 has better regulation efficiency and heat compensation efficiency on the flue gas temperature after the CO catalytic regenerative heat exchange device compared with Example 2.

Example 3

[0090] This example provides a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, which only differs from Example 1 in that: the usage amount of the CO heat-regenerative catalyst was 128 m.sup.3, the heat exchange area of the heat exchange element on the raw flue gas side was about 26000 m.sup.2, and the heat exchange area of the heat exchange element on the purified flue gas side was about 40000 m.sup.2 (estimated based on the flow rate of the sintering flue gas of 850000 Nm.sup.3/h).

Example 4

[0091] This example provides a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, which only differs from Example 1 in that: the usage amount of the CO heat-regenerative catalyst was 170 m.sup.3, the heat exchange area of the heat exchange element on the raw flue gas side was about 20000 m.sup.2, and the heat exchange area of the heat exchange element on the purified flue gas side was about 30000 m.sup.2 (estimated based on the flow rate of the sintering flue gas of 850000 Nm.sup.3/h), the porosity of the cordierite honeycomb ceramic heat-regenerative framework was 0.5, and the size of the catalyst was 100 mm100 mm40 mm.

Example 5

[0092] This example provides a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, which only differs from Example 1 in that: the porosity of the cordierite honeycomb ceramic heat-regenerative framework was 0.3.

Comparative Example 1

[0093] This comparative example provides a device system for medium/low-temperature SCR denitration. In the device system, the CO catalytic regenerative heat exchange device was not provided, and only a heat exchanger having a heat exchange element with the same structure as in Example 1 was provided. However, the heat exchange area of the heat exchange element on the raw flue gas side was about 60000 m.sup.2, and the heat exchange area of the heat exchange element on the purified flue gas side was about 90000 m.sup.2 (estimated based on the flow rate of the sintering flue gas of 850000 Nm.sup.3/h). In addition, other components, locations, and structures were the same as those in Example 1.

Comparative Example 2

[0094] This comparative example provides a device system for medium/low-temperature SCR denitration. In the device system, the CO catalytic regenerative heat exchange device was not provided, instead, it was replaced by a heat exchanger (the structure of the heat exchange element was the same as that of Example 1, the heat exchange area of the heat exchange element on the raw flue gas side was about 40000 m.sup.2, and the heat exchange area of the heat exchange element on the purified flue gas side was about 90000 m.sup.2) and a CO catalytic oxidation device (the active component for CO catalytic oxidation was a precious metal platinum catalyst, a non-heat-regenerative catalyst) which were arranged in series sequentially, and the denitrated flue gas only passed through the heat exchanger, and did not pass through the CO catalytic oxidation device. In addition, other components, locations, and structures were the same as those in Example 1.

Comparative Example 3

[0095] This comparative example provides a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, the device system was the same as in Example 2 except that only the CO heat-regenerative catalyst was arranged (the usage amount of the CO heat-regenerative catalyst was the same as that in Example 2), the heat exchange element was not arranged, and the purified flue gas outlet of the medium/low-temperature SCR denitration reaction device was not connected with the denitrated flue gas inlet of the CO catalytic regenerative heat exchange device, but was directly discharged externally.

Comparative Example 4

[0096] This comparative example provides a device system for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, the device system was the same as that in Example 2 except that only the CO heat-regenerative catalyst was arranged (the usage amount of the CO heat-regenerative catalyst was 160 m.sup.3), and the heat exchange element was not arranged, and the purified flue gas outlet of the medium/low-temperature SCR denitration reaction device was still connected with the denitrated flue gas inlet of the CO catalytic regenerative heat exchange device.

[0097] In Comparative Example 4, the usage amount of CO heat-regenerative catalyst was increased to replace the heat exchange element in Example 2, and the final pressure drop was decreased. However, due to the lower heat exchange efficiency of the CO heat-regenerative catalyst compared with that of the heat exchange element, the usage amount of the blast furnace gas will increase.

Application Example 1

[0098] This application example provides a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, and the method was performed with the device in Example 1, which comprised the following steps: [0099] (1) the sintering flue gas (the flue gas of 240 m.sup.2 sintering machine, a flow rate of 850000 Nm.sup.3/h, a temperature of 100 C., a CO concentration of 8000 mg/m.sup.3, a particulate matter concentration of 2 mg/Nm.sup.3, a NO.sub.x concentration of 300 mg/Nm.sup.3, and a SO.sub.2 concentration of 16 mg/Nm.sup.3) was subjected to the first CO catalytic conversion by the CO catalytic regenerative heat exchange device, and the sintering flue gas was heated to 250 C., and then introduced into the hot blast furnace device for heat compensation to 280 C. to obtain the heated flue gas; [0100] (2) the heated flue gas was mixed with an ammonia source by the ammonia spray device, and then introduced into a medium/low-temperature SCR denitration reaction device to perform the SCR denitration reaction (the denitration catalyst was V.sub.2O.sub.5WO.sub.3/TiO.sub.2), and the NO.sub.x in the flue gas reacted with a reducing agent to generate N.sub.2 to obtain the denitrated flue gas of 275 C.; and [0101] (3) the denitrated flue gas was introduced into the CO catalytic regenerative heat exchange device, and subjected to heat exchange cooling and a second CO catalytic conversion to obtain the purified sintering flue gas of 110 C.; [0102] after a cycle of step (1) to step (3), the CO heat-regenerative catalyst and the heat exchange element that stored heat were transferred around the guide bearing to the sintering flue gas side, i.e., cycling back to step (1), the CO heat-regenerative catalyst and the heat exchange element released heat to raise the temperature of the sintering flue gas;

[0103] when the system device was running stably, the heat of the denitrated flue gas was stored in the CO heat-regenerative catalyst and the heat exchange element by the CO catalytic regenerative heat exchange device to transfer to the sintering flue gas, in which case, the fuel feed was stopped, and the hot blast furnace device was shut down; by the CO catalytic regenerative heat exchange device, the first CO catalytic conversion was performed and the temperature of the sintering flue gas can be raised to 280 C.

Application Example 2

[0104] This application example provides a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration, and the method was performed with the device in Example 2, which comprised the following steps: [0105] (1) when the device was started, the sintering flue gas (the flue gas of 240 m.sup.2 sintering machine, a flow rate of 850000 Nm.sup.3/h, a temperature of 110 C., a CO concentration of 8000 mg/m.sup.3, a particulate matter concentration of 3 mg/Nm.sup.3, a NO.sub.x concentration of 280 mg/Nm.sup.3, and a SO.sub.2 concentration of 18 mg/Nm.sup.3) was introduced into the hot blast furnace device and heated to 260 C., then subjected to the first CO catalytic conversion by the CO catalytic regenerative heat exchange device, and the sintering flue gas was heated to 280 C. to obtain the heated flue gas; [0106] (2) the heated flue gas was mixed with an ammonia source by the ammonia spray device, and then passed into a medium/low-temperature SCR denitration reaction device to perform the SCR denitration reaction (the denitration catalyst was V.sub.2O.sub.5WO.sub.3/TiO.sub.2), and the NO.sub.x in the flue gas reacted with a reducing agent to generate N.sub.2 to obtain the denitrated flue gas of 278 C.; and [0107] (3) the denitrated flue gas was fed into the CO catalytic regenerative heat exchange device, and subjected to heat exchange cooling and a second CO catalytic conversion to obtain the purified sintering flue gas of 116 C.; [0108] after a cycle of step (1) to step (3), the CO heat-regenerative catalyst and the heat exchange element that store heat were transferred around the guide bearing to the sintering flue gas side, i.e., cycling back to step (1), the CO heat-regenerative catalyst and the heat exchange element released heat to raise the temperature of the sintering flue gas; [0109] when the system device was running stably, the heat of the denitrated flue gas was stored in the CO heat-regenerative catalyst and the heat exchange element by the CO catalytic regenerative heat exchange device to transfer to the sintering flue gas, in which case, the fuel feed was stopped, and the hot blast furnace device was shut down; by the CO catalytic regenerative heat exchange device, the first CO catalytic conversion was performed and the temperature of the sintering flue gas can be raised to 280 C.

Application Example 3

[0110] This application example provides a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration. The method was performed with the device in Example 3, the method had the same steps as in Application Example 1, and the difference is only in that the first CO catalytic conversion was performed by the CO catalytic regenerative heat exchange device, and the sintering flue gas was heated to 254 C., the flue gas was heated to 286 C. by the hot blast furnace device with blast furnace gas introduced, and then introduced into the ammonia spray device, the denitrated flue gas of 278 C. was discharged from the medium/plow-temperature SCR denitration reaction device, and the denitrated flue gas was introduced into the CO catalytic regenerative heat exchange device, and was subjected to heat exchange cooling and the second CO catalytic conversion to obtain the purified sintering flue gas with a temperature of 113 C.

Application Example 4

[0111] This application example provides a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration. The method was performed on the device in Example 4, the method had the same steps as in Application Example 1, and the difference is only in that the sintering flue gas with a temperature of 80 C. was subjected to the first CO catalytic conversion by the CO catalytic regenerative heat exchange device, and heated to 242 C., then the flue gas was heated to 270 C. by the hot blast furnace device with the blast furnace gas introduced, and then introduced into the ammonia spray device, the denitrated flue gas of 267 C. was discharged from the medium/low-temperature SCR denitration reaction device, and the denitrated flue gas was introduced into the CO catalytic regenerative heat exchange device, and was subjected to heat exchange cooling and the second CO catalytic conversion to obtain the purified sintering flue gas with a temperature of 107 C.

Application Example 5

[0112] This application example provides a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration. The method was performed on the device in Example 5, the method had the same steps as in Application Example 1, and the difference was only in that the first CO catalytic conversion was performed by the CO catalytic regenerative heat exchange device, and the sintering flue gas was heated to 252 C., the flue gas was heated to 280 C. by hot blast furnace device with the blast furnace gas introduced, and then introduced into the ammonia spray device.

Application Example 6

[0113] This application example provides a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration. The method was performed on the device in Example 1, the method had the same steps as in Application Example 1, and the difference was only in that the sintering flue gas with a temperature of 80 C. was subjected to the first CO catalytic conversion by the CO catalytic regenerative heat exchange device and heated to 242 C., the flue gas was heated to 270 C. by the hot blast furnace device with the blast furnace gas introduced, and then introduced into the ammonia spray device, the denitrated flue gas of 267 C. was discharged from the medium/low-temperature SCR denitration reaction device, and the denitrated flue gas was introduced into the CO catalytic regenerative heat exchange device, and was subjected to heat exchange cooling and the second CO catalytic conversion to obtain the purified sintering flue gas with a temperature of 106 C.

Application Comparative Example 1

[0114] This application comparative example provides a method for sintering flue gas having medium/low-temperature SCR denitration. The method was performed with the device in Comparative Example 1, and the method specially comprised the following steps: [0115] (1) the sintering flue gas (the flue gas of 240 m.sup.2 sintering machine, a flow rate of 850000 Nm.sup.3/h, a temperature of 100 C., a CO concentration of 8000 mg/m.sup.3, a particulate matter concentration of 2 mg/Nm.sup.3, a NO.sub.x concentration of 300 mg/Nm.sup.3, and a SO.sub.2 concentration of 16 mg/Nm.sup.3) was introduced into a heat exchanger and heated to 250 C., and then introduced into a hot blast furnace device for heat compensation to 280 C. to obtain the heated flue gas; [0116] (2) the heated flue gas was mixed with an ammonia source by the ammonia spray device, and then introduced into the medium/low-temperature SCR denitration reaction device to perform the SCR denitration reaction (the denitration catalyst was V.sub.2O.sub.5WO.sub.3/TiO.sub.2), and the NO.sub.x in the flue gas reacted with a reducing agent to generate N.sub.2 to obtain the denitrated flue gas of 275 C.; and [0117] (3) the denitrated flue gas was introduced into a heat exchanger, and subjected to heat exchange cooling to obtain the purified sintering flue gas of 110 C.

[0118] In this comparative example, the heat exchange area of the heat exchange element on the raw flue gas side was about 60000 m.sup.2, and the heat exchange area of the heat exchange element on the purified flue gas side was about 90000 m.sup.2 (estimated based on the flow rate of the sintering flue gas of 850000 Nm.sup.3/h), the blast furnace gas was required to be introduced constantly, and the operation cost was high.

Application Comparative Example 2

[0119] This application comparative example provides a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration. The method was performed with the device in Comparative Example 2, and the method differed from Application Example 1 only in that the sintering flue gas was first subjected to heat exchange by the heat exchanger, and then subjected to the first CO catalytic conversion by the CO catalytic device and the sintering flue gas was heated to 232 C., and then the flue gas was heat to 280 C. by the hot blast furnace device with the blast furnace gas introduced, and then introduced into the ammonia spray device, the denitrated flue gas at 275 C. was discharged from the medium/low-temperature SCR denitration reaction device, and the denitrated flue gas was introduced into the CO catalytic regenerative heat exchange device, and subjected to heat exchange cooling and the second CO catalytic conversion to obtain the purified sintering flue gas with a temperature of 111 C. In this comparative example, constant heat compensation by the blast furnace gas was not required.

Application Comparative Example 3

[0120] This application comparative example provides a method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration. The method was performed on the device in Comparative Example 3, and the others were the same as in Application Example 1, which specifically comprised: [0121] (1) the sintering flue gas (the flue gas of 240 m.sup.2 sintering machine, a flow rate of 850000 Nm.sup.3/h, a temperature of 100 C., a CO concentration of 8000 mg/m.sup.3, a particulate matter concentration of 2 mg/Nm.sup.3, a NO.sub.x concentration of 300 mg/Nm.sup.3, and a SO.sub.2 concentration of 16 mg/Nm.sup.3) was heated to 230 C. by a hot blast furnace device, and then introduced into a CO catalytic device, and the sintering flue gas was heated to 280 C. by the heat release from catalytic oxidation; and [0122] (2) the heated flue gas was mixed with an ammonia source by the ammonia spray device, and then introduced into the medium/low-temperature SCR denitration reaction device to perform the SCR denitration reaction (the denitration catalyst was V.sub.2O.sub.5WO.sub.3/TiO.sub.2), and the NO.sub.x in the flue gas reacted with a reducing agent to generate N.sub.2 to obtain the denitrated flue gas at 275 C.

[0123] In this comparative example, the raw flue gas and the purified flue gas were not subjected to heat exchange, and the blast furnace gas was required to be introduced constantly for heat compensation to raise the temperature to reach the CO catalytic reaction temperature, and the system pressure drop was small, but the operation cost was high.

[0124] The NO.sub.x concentration and the CO concentration in the purified flue gas were detected with the infrared flue gas analyzer, the system pressure drop was evaluated by the pressure gauges before and after the system, and the fuel consumption in the hot blast furnace device for 30 days of operation was calculated by the flow rate of the blast furnace gas. The results are shown in Table 1.

TABLE-US-00001 TABLE 1 NO.sub.x CO concentration Total pressure Blast furnace gas concentration in in purified drop in the consumption (30 purified flue gas flue gas system days) Application 28 mg/m.sup.3 420 mg/m.sup.3 1700 Pa 30000 m.sup.3 Example 1 Application 29 mg/m.sup.3 460 mg/m.sup.3 1720 Pa 40000 m.sup.3 Example 2 Application 32 mg/m.sup.3 360 mg/m.sup.3 1680 Pa 36000 m.sup.3 Example 3 Application 38 mg/m.sup.3 320 mg/m.sup.3 1850 Pa 50000 m.sup.3 Example 4 Application 27 mg/m.sup.3 260 mg/m.sup.3 2100 Pa 28000 m.sup.3 Example 5 Application 40 mg/m.sup.3 520 mg/m.sup.3 1730 Pa 39000 m.sup.3 Example 6 Application 36 mg/m.sup.3 8000 mg/m.sup.3 2250 Pa 8000000 m.sup.3 Comparative Example 1 Application 34 mg/m.sup.3 800 mg/m.sup.3 2380 Pa 200000 m.sup.3 Comparative Example 2 Application 35 mg/m.sup.3 400 mg/m.sup.3 600 Pa 24000000 m.sup.3 Comparative Example 3

[0125] From the data in Table (1), the following points can be found: [0126] (1) by analyzing Application Examples 1-4, it can be seen that the pressure drop of the method for sintering flue gas having CO catalytic heat exchange in series with medium/low-temperature SCR denitration provided in the present application is low; for the flue gas flow rate of 850000 Nm.sup.3/h, the total pressure drop of the system is only less than or equal to 1900 Pa, and the consumption of blast furnace gas is low, which is less than or equal to 50000 m.sup.3 in 30 days, the result of denitration and CO removal are excellent, wherein the NO.sub.x concentration in the purified flue gas is less than or equal to 40 mg/m.sup.3, and the CO concentration in the purified flue gas is less than or equal to 500 mg/m.sup.3; [0127] (2) by analyzing Application Example 1 and Application Example 5, it can be seen that the porosity of the cordierite honeycomb ceramic heat-regenerative framework in Application Example 1 is 0.6, while the porosity is 0.3 in Application Example 5, and in Application Example 5, the pressure drop increases significantly to 2100 Pa, and the denitration efficiency is not significantly optimized, resulting in a significant increase in the system operation cost; it is shown that in the present application, the porosity of the cordierite honeycomb ceramic heat-regenerative framework is preferably controlled within a specific range, which can better ensure the efficiency of denitration and CO removal while reducing the system pressure drop and the cost; [0128] (3) by analyzing Application Example 1 and Application Comparative Example 1, it can be seen that in order to achieve the same heat exchange result in Application Example 1, the area of the heat exchange element is required to be significantly increased in Application Comparative Example 1, resulting in a significant increase in the pressure drop to 2250 Pa, the overall system no longer has the efficiency of CO removal, and the blast furnace gas consumption is as high as 8000000 m.sup.3/30 days, which shows that in the present application, the pressure drop and the blast furnace gas consumption are significantly reduced by adopting the CO catalytic regenerative heat exchange device with a heat storage function; [0129] (4) by analyzing Application Example 1 and Application Comparative Example 2, it can be seen that only one CO catalytic oxidation device is added on the basis of the original heat exchanger, resulting in a significant increase in the system pressure drop, and the required blast furnace gas consumption is still high; and [0130] (5) by analyzing Application Example 1 and Application Comparative Example 3, it can be seen that in Application Comparative Example 3, only the CO heat-regenerative catalyst is provided, the pressure drop decreases, but the purified flue gas outlet is no connected to the CO catalytic heat-regenerative device, so that the blast furnace gas is continuously operated and has a huge consumption. Moreover, the flue gas does not undergo two times of CO catalysis; the catalytic efficiency on CO is reduced.

[0131] The detailed structural features in the present application are illustrated by the above examples in the present application, but the present application is not limited to the above detailed structural features, that is, the present application does not necessarily rely on the above detailed structural features to be implemented. Those skilled in the art should understand that any improvement of the present application, the equivalent substitution of selected parts, the addition of auxiliary ingredients, and the selection of specific methods in the present application shall fall within the protection scope and disclosure scope of the present application.