Exhaust gas post-processing system

Abstract

An exhaust gas post-processing system includes an oxidation catalyst configured to oxidize substances included in the exhaust gas; a diesel particulate filter configured to collect particulate matters included in the exhaust gas and disposed subsequent to the oxidation catalyst; a dosing module configured to inject a reducing agent and disposed subsequent to the diesel particulate filter; and a selective catalytic reduction configured to remove nitrogen oxide using the reducing agent included in the exhaust gas and disposed subsequent to the dosing module. The diesel particulate filter includes a catalytic component represented by La.sub.1-xAg.sub.xMnO.sub.3 (where 0<x<1).

Claims

1. An exhaust gas post-processing system, comprising: an oxidation catalyst configured to oxidize substances included in the exhaust gas; a diesel particulate filter configured to collect particulate matters included in the exhaust gas and disposed subsequent to the oxidation catalyst; a dosing module configured to inject a reducing agent and disposed subsequent to the diesel particulate filter; and a selective catalytic reduction configured to remove nitrogen oxide using the reducing agent included in the exhaust gas and disposed subsequent to the dosing module, wherein the diesel particulate filter includes a catalytic component represented by La.sub.1-xAg.sub.xMnO.sub.3 (where 0<x<1), and wherein the selective catalytic reduction includes V.sub.2O.sub.5WO.sub.3/TiO.sub.2.

2. The exhaust gas post-processing system of claim 1, wherein: the diesel particulate filter includes a catalyst component represented by La.sub.1-xAg.sub.xMnO.sub.3 (where 0.2x0.8).

3. The exhaust gas post-processing system of claim 1, wherein: the oxidation catalyst includes a catalyst component consisting of platinum and palladium.

4. The exhaust gas post-processing system of claim 1, wherein: the reducing agent includes urea.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a schematic diagram of an exhaust gas post-processing system according to an exemplary embodiment of the present invention.

(2) FIG. 2 is a graph illustrating reaction temperatures and a conversion of nitrogen monoxide of a diesel particulate filter in Examples 1 to 4 and Comparative Example 1.

(3) FIG. 3 is a graph illustrating a conversion of nitrogen oxide in the exhaust gas post-processing system according to Examples 1 to 3.

DETAILED DESCRIPTION OF THE EMBODIMENTS

(4) Various advantages and features of the present inventive concept and methods accomplishing thereof will become apparent from the following description of embodiments with reference to the accompanying drawings. However, the present inventive concept is not limited to the embodiments set forth herein but may be implemented in many different forms. The present embodiments may be provided so that the disclosure of the present invention will be complete, and will fully convey the scope of the invention to those skilled in the art and therefore the present invention will be defined within the scope of claims. Throughout the specification, like reference numerals denote like elements.

(5) Accordingly, technologies well known in some exemplary embodiments are not described in detail to avoid an obscure interpretation of the present invention. Unless defined otherwise, it is to be understood that all the terms (including technical and scientific terms) used in the specification has the same meaning as those that are understood by those who skilled in the art. Throughout the specification, unless explicitly described to the contrary, the word comprise and variations such as comprises or comprising, will be understood to imply the inclusion of stated elements but not the exclusion of any other elements. Further, unless explicitly described to the contrary, a singular form includes a plural form in the present specification.

(6) FIG. 1 is a schematic diagram of an exhaust gas post-processing system according to an exemplary embodiment of the present invention.

(7) Referring to FIG. 1, the exhaust gas post-processing system includes an engine 100, an exhaust line 110, an oxidation catalyst 120, a diesel particulate filter 130, a dosing module 140, and a selective catalytic reduction 150.

(8) The oxidation catalyst 120, the diesel particulate filter 130, the dosing module 140, and the selective catalytic reduction 150 are sequentially disposed in the exhaust line 110 and the exhaust gas is purified by them before being emitted to the outside.

(9) The oxidation catalyst 120 oxidizes hydrocarbons and carbon monoxide included in the exhaust gas, and the diesel particulate filter 130 collects particulate matters included in the exhaust gas and burns them under a predetermined temperature condition to be removed.

(10) Further, the oxidation catalyst 120 converts nitrogen monoxide (NO) included in the exhaust gas into nitrogen dioxide (NO.sub.2) and the diesel particulate filter 130 naturally regenerates the collected particulate matter by increasing the temperature by the oxidation reaction of the oxidation catalyst 120.

(11) The oxidation catalyst 120 may include a catalyst component consisting of platinum (Pt) and palladium (Pd). In detail, the oxidation catalyst 120 may include a catalyst component in which a molar ratio of platinum (Pt) and palladium (Pd) is 4:1.

(12) According to the exemplary embodiment of the present invention, the diesel particulate filter 130 includes the catalyst component represented by La.sub.1-xAg.sub.xMnO.sub.3 (where 0<x<1), in which the catalyst component oxidizes the nitrogen monoxide included in the exhaust gas into the nitrogen dioxide to be supplied to a later stage. Here, the selective catalytic reduction 150 uses the nitrogen dioxide supplied from the diesel particulate filter 130 to maximize purification efficiency of the nitrogen oxide.

(13) The oxidation of the particulate matter is also promoted by a reaction of the nitrogen dioxide with the particulate matter while the nitrogen monoxide is being oxidized into nitrogen dioxide.

(14) The catalyst component represented by La.sub.1-xAg.sub.xMnO.sub.3 (where 0<x<1) increases a conversion of the nitrogen monoxide in, in particular, a low temperature area of 200 to 300 C. In more detail, the diesel particulate filter may include a catalyst component represented by La.sub.1-xAg.sub.xMnO.sub.3 (however, 0.2x0.8).

(15) The dosing module 140 injects a reducing agent into the exhaust line 110, in which the reducing agent may include urea. The selective catalytic reduction 150 uses the reducing agent injected from the dosing module 140 to remove the nitrogen oxide included in the exhaust gas.

(16) The selective catalytic reduction 150 uses the nitrogen dioxide supplied from the diesel particulate filter 130 to maximize purification efficiency of the nitrogen oxide. In detail, the selective catalytic reduction may include a catalyst component consisting of at least one selected from V.sub.2O.sub.5, WO.sub.3, Cu and Fe. In more detail, the selective catalytic reduction may include V.sub.2O.sub.5WO.sub.3/TiO.sub.2, Cu-zeolite, or Fe-zeolite.

(17) When a volume ratio of the nitrogen monoxide and the nitrogen dioxide in the exhaust gas at a front stage of the selective catalytic reduction 150 is 1:1, the purification efficiency of the nitrogen oxide is improved in the low temperature area of 200 to 350 C. due to an SCR reaction.

(18) According to the exemplary embodiment of the present invention, the purification efficiency of the nitrogen oxide of the selective catalytic reduction 150 is improved by supplying the nitrogen dioxide (NO.sub.2) to the later stage by the catalyst component included in the diesel particulate filter 130.

(19) Hereinafter, various Examples of the prevent inventive concept and Comparative Example will be described. However, the following Examples are only the preferred Examples and therefore the present invention is not limited to the following Examples.

Preparation Example: Preparing of Perovskite Monolith-Type Catalytic Reactor

(20) A perovskite monolith-type catalytic reactor for NO oxidation performance evaluation coats a cordierite substrate with perovskite by a general dipping method. The cordierite substrate used for coating used a 400 cpsi cell monolith having a diameter of 0.7 in and a height of 0.57 in. Dipping.fwdarw.air blowing.fwdarw.drying (110 C.) were repeated on slurry prepared by mixing perovskite catalyst and distilled water at a predetermined ratio and performing ball-milling thereon until 40 wt % against the cordierite is supported in the substrate. Finally, the coated monolith catalytic reactor was fired for five hours under air atmosphere of 700 C. and then the NO oxidation performance evaluation was performed by the following evaluation method.

Evaluation Method: NO Oxidation Performance Evaluation

(21) The NO oxidation performance evaluation was performed in a fixed bed continuous flow reactor system and used the monolith-type catalytic reactor upon the evaluation. The injected reaction gas concentration was NO of 400 ppm, O.sub.2 of 8%, H.sub.2O of 10%, and a balance of N.sub.2, the reactor space speed was maintained at 30,000 h.sup.1 upon the evaluation, and a change in the reaction gas concentration after and before the reaction was analyzed by an FT-IR (Nicolet 6700, Thermo Electronic Co.) connected to the reactor online.

Example 1

(22) The exhaust gas including NO of 400 ppm as a volume %, O.sub.2 of 8%, H.sub.2O of 10%, and a balance of N.sub.2 was supplied to the monolith catalyst coated with a La.sub.0.9Ag.sub.0.1MnO.sub.3 catalyst at a space speed of 30,000 h.sup.1.

(23) A conversion of NO for each temperature was measured by the foregoing evaluation method and the measurement results were shown in FIG. 2.

Example 2

(24) Example 2 was performed by the same method as Example 1 except that the monolith catalyst coated with the La.sub.0.8Ag.sub.0.2MnO.sub.3 catalyst was prepared.

(25) The conversion of NO for each temperature was measured by the foregoing evaluation method and the measurement results were shown in FIG. 2.

Example 3

(26) Example 3 was performed by the same method as Example 1 except that the monolith catalyst coated with an La.sub.0.5Ag.sub.0.5MnO.sub.3 catalyst was prepared.

(27) The conversion of NO for each temperature was measured by the foregoing evaluation method and the measurement results were shown in FIG. 2.

Example 4

(28) Example 4 was performed by the same method as Example 1 except that the monolith catalyst coated with the La.sub.0.2Ag.sub.0.8MnO.sub.3 catalyst was prepared.

(29) The conversion of NO for each temperature was measured by the foregoing evaluation method and the measurement results were shown in FIG. 2.

Comparative Example 1

(30) Comparative Example 1 was performed by the same method as Example 1 except that the monolith catalyst coated with the La.sub.0.9Sr.sub.0.1MnO.sub.3 catalyst was prepared.

(31) The conversion of NO for each temperature was measured by the foregoing evaluation method and the measurement results were shown in FIG. 2.

(32) It could be appreciated from FIG. 2 that the monolith catalyst coated with the perovskite manufactured in Examples 1 to 4 has the excellent conversion of the nitrogen monoxide and in particular, has the more excellent conversion in the low temperature area of 200 to 300 C.

Experimental Example 1: Nitrogen Oxide Removal Experiment

(33) The exhaust gas including NO of 400 ppm as a volume %, O.sub.2 of 8%, H.sub.2O of 10%, and a balance of N.sub.2 was supplied to 1.1 cc of the La.sub.0.5Ag.sub.0.5MnO.sub.3 catalyst prepared at a 20/30 mesh at a space speed of 60,000 h.sup.1 at 250 C. The passing exhaust gas was added with the reaction gas so that the whole reaction gas becomes NH.sub.3 of 500 ppm, NOx of 500 ppm, O.sub.2 of 5.6%, H.sub.2O of 10%, and a balance of N.sub.2 to flow in 0.95 cc of V.sub.2O.sub.5WO.sub.3/TiO.sub.2 selective catalytic reduction prepared at the 20/30 mesh at a space speed of 100,000 h.sup.1.

(34) The conversion of nitrogen oxide (NOx) of the exhaust gas passing through the selective catalytic reduction was measured and the measured results were shown in FIG. 3.

Experimental Example 2

(35) The La.sub.0.5Ag.sub.0.5MnO.sub.3 catalyst was not disposed at a front stage of the selective catalytic reduction and only the V.sub.2O.sub.5WO.sub.3/TiO.sub.2 selective catalytic reduction was disposed.

(36) The exhaust gas including NH.sub.3 of 500 ppm as a volume %, NO of 500 ppm, O.sub.2 of 5%, H.sub.2O of 10%, and a balance of N.sub.2 was supplied to the selective catalytic reduction at the space speed of 100,000 h.sup.1.

(37) The conversion of nitrogen oxide (NOx) of the exhaust gas passing through the selective catalytic reduction was measured and the measured results were shown in FIG. 3.

Experimental Example 3

(38) The La.sub.0.5Ag.sub.0.5MnO.sub.3 catalyst was not disposed at a front stage of the selective catalytic reduction and only the V.sub.2O.sub.5WO.sub.3/TiO.sub.2 selective catalytic reduction was disposed.

(39) The exhaust gas including NH.sub.3 of 500 ppm as a volume %, NO of 250 ppm, NO.sub.2 of 250 ppm, O.sub.2 of 5%, H.sub.2O of 10%, and a balance of N.sub.2 was supplied to the selective catalytic reduction at the space speed of 100,000 h.sup.1.

(40) The conversion of nitrogen oxide (NOx) of the exhaust gas passing through the selective catalytic reduction was measured and the measured results were shown in FIG. 3.

(41) It could be confirmed from FIG. 3 that the conversion of the nitrogen oxide of the exhaust gas post-processing system including the La.sub.0.5Ag.sub.0.5MnO.sub.3 catalyst at the front stage of the selective catalytic reduction may have the excellent conversion of the nitrogen oxide and approximately the same conversion as Experimental Example 3 in which the volume ratio of nitrogen monoxide and nitrogen dioxide is controlled to be 1:1 may be obtained. In particular, it could be confirmed that the conversion of the nitrogen oxide is excellent in the low temperature area of 250 to 350 C.

(42) The regeneration Experiment of the particulate matters used the diesel engine to measure the purification performance of PM after 60 minutes and 12 minutes are maintained under the condition that the temperature of the front stage of the DPF is 350 C. and 640 C., respectively. The evaluation layout is configured of a DOC+DPF system, the DOC catalyst uses the monolith catalyst coated with a catalyst having a noble metal ratio of 2 Pt/1 Pd, the DPF coated with a noble metal catalyst having a noble metal ratio of 1 Pt/1 Pd, the La.sub.0.5Ag.sub.0.5MnO.sub.3 catalyst, an Ag/CeO.sub.2 catalyst, respectively, was used to perform the comparison evaluation.

Experimental Example 4: Particulate Matter Regeneration Experiment

(43) The DPF coated with the noble catalyst having 1 Pt/1 Pd measured the particulate matter regeneration result and the measured results were arranged in the following Table 1.

Experimental Example 5

(44) The DPF coated with the La.sub.0.5Ag.sub.0.5MnO.sub.3 catalyst measured the particulate matter regeneration result and the measured results were arranged in the following Table 1.

Experimental Example 6

(45) The DPF coated with the Ag/CeO.sub.2 catalyst measured the particulate matter regeneration result and the measured results were arranged in the following Table 1.

(46) TABLE-US-00001 TABLE 1 Regeneration Regeneration at 350 C. at 640 C. Experimental Example 4 20% 70% Experimental Example 5 30% 69% Experimental Example 6 17% 64%

(47) As illustrated in the above Table 1, in the Experimental Example 4, it could be confirmed that the regeneration rates are equal or excellent at both of the temperatures of 350 C. and 640 C. and, in particular, the regeneration ratios are excellent in a region of 350 C.

(48) As the NO is oxidized into the NO.sub.2 in the diesel particulate filter according to the exemplary embodiment of the present invention, it may be confirmed that the particulate matters are oxidized by the reaction of the particulate material with the NO.sub.2.

(49) The present invention is not limited to the above Examples but may be manufactured in different various forms and it may be understood that a person having ordinary skilled in the art to which the present invention pertains may perform the present invention other detailed forms without changing the technical ideas or the essential features of the present invention. Therefore, it should be understood that the above-mentioned embodiments are not restrictive but are exemplary in all aspects.

(50) While this invention has been described in connection with what is presently considered to be practical exemplary embodiments, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.