Patent Application
20180149055
The present application claims priority to Korean Patent Application No. 10-2016-0159258 filed on Nov. 28, 2016, the entire contents of which are incorporated herein for all purposes by this reference.
The present invention relates to a device for purifying exhaust gas, and more particularly, to a device for purifying exhaust gas capable of reducing harmful materials in exhaust gas by using an LTA zeolite catalyst with improved high-temperature performance.
In general, an exhaust system of an engine includes an exhaust gas post-processing device such as a diesel oxidation catalyst (DOC), a diesel particulate matter filter (DPF), a selective catalyst reduction (SCR), and a lean NOx trap (LNT) catalyst to reduce carbon monoxide (CO), hydrocarbons (HC), a particulate matter, nitrogen oxide (NOx), and the like which are pollutants contained in the exhaust gas.
The DOC may oxidize total hydrocarbon and carbon monoxide in the exhaust gas and oxidize nitrogen monoxide into nitrogen dioxide.
The DPF may collect a particulate material contained in the exhaust gas and purify the particulate material through a chemical conversion process.
Further, in the SCR, a reducing agent (urea) injected in a stream direction of the exhaust gas through an injector is converted into ammonia (NH3) by the heat of the exhaust gas, and as a catalytic reaction of nitrogen oxide and ammonia in exhaust gas by the SCR catalyst, nitrogen oxide is reduced to nitrogen gas (N2) and water (H2O).
In addition, recently, as emissions regulations for the vehicle are enhanced, improvement in nitrogen oxide purification performance for the SCR system is required. Particularly, in a gasoline engine with an exhaust gas of high temperature, a technique for improving heat durability of the catalyst or improving nitrogen oxide purification purify efficiency due to low heat resistance characteristic of the SCR system is required.
The information disclosed in this Background of the Invention section is only for enhancement of understanding of the general background of the invention and should not be taken as an acknowledgement or any form of suggestion that this information forms the prior art already known to a person skilled in the art.
Various aspects of the present invention are directed to providing exhaust gas purification performance by improving the high-temperature performance of a SCR and a SGPF by applying an LTA zeolite catalyst to a SCR and a SGPF.
A device for purifying exhaust gas is provided to purify exhaust gas in an engine, the device including: an exhaust line through which exhaust gas discharged from the engine passes; a warm-up catalytic converter (WCC) that is disposed in the exhaust line; and a catalyst device disposed in the rear of the warm-up catalytic converter configured for reducing nitrogen oxide of the exhaust gas passing through the warm-up catalytic converter, wherein the catalyst device includes an LTA zeolite catalyst.
A ratio of copper and aluminum of the LTA zeolite catalyst may be 11 to 16.
The content of copper may be 0.5 wt % to 5 wt % with respect to the entire weight of the LTA zeolite catalyst.
The device may further include an under floor catalytic converter disposed in the rear of the catalyst device.
The warm-up catalytic converter or the under floor catalytic converter may include a three-way catalyst converting toxic materials including a carbon monoxide, a hydrocarbon, and a nitrogen oxide included in the exhaust gas into harmless substances by an oxidation and reduction reaction.
The catalyst device may include a selective catalyst reduction (SCR).
The catalyst device may include an SGPF (SCR on GPF) coated with a selective catalyst reduction (SCR) on a gasoline particulate filter (GPF).
According to the exemplary embodiment of the present invention, the LTA zeolite catalyst with improved high-temperature performance is applied the SCR or the SGPF, and thus it is possible to provide an environment that can increase the heat resistance of the catalyst in a gasoline engine, improve the nitrogen oxide purification performance, and improve fuel economy.
The methods and apparatuses of the present invention have other features and advantages which will be apparent from or are set forth in more detail in the accompanying drawings, which are incorporated herein, and the following Detailed Description, which together serve to explain certain principles of the present invention.
It should be understood that the appended drawings are not necessarily to scale, presenting a somewhat simplified representation of various features illustrative of the basic principles of the invention. The specific design features of the present invention as disclosed herein, including, for example, specific dimensions, orientations, locations, and shapes will be determined in part by the particular intended application and use environment.
In the figures, reference numbers refer to the same or equivalent parts of the present invention throughout the several figures of the drawing.
Reference will now be made in detail to various embodiments of the present invention(s), examples of which are illustrated in the accompanying drawings and described below. While the invention(s) will be described in conjunction with exemplary embodiments, it will be understood that the present description is not intended to limit the invention(s) to those exemplary embodiments. On the contrary, the invention(s) is intended to cover not only the exemplary embodiments, but also various alternatives, modifications, equivalents and other embodiments, which may be included within the spirit and scope of the invention as defined by the appended claims.
A device for purifying exhaust gas according to an exemplary embodiment of the present invention may be applied to not only vehicles but also various devices which burn fossil fuels to obtain energy and emit gas generated in the process. In the present specification, it is exemplified that the device for purifying exhaust gas is applied to the vehicles, but it should not be interpreted that the device for purifying exhaust gas is applied to only the vehicles.
An engine for generating power is mounted on the vehicle. The engine converts chemical energy into mechanical energy by burning a mixture of fuel and air. The engine is connected to an intake manifold to receive air into a combustion chamber, and connected to an exhaust manifold to collect the exhaust gas generated in the combustion process in the exhaust manifold and discharge the collected exhaust gas to the outside of the vehicle. In the combustion chamber or the intake manifold, an injector is disposed to inject the fuel into the combustion chamber or the intake manifold.
The exhaust gas generated in the engine is discharged to the outside of the vehicle through the exhaust manifold. The exhaust device may include an exhaust pipe and an exhaust gas recirculation (EGR) device.
The exhaust pipe is connected to the exhaust manifold to discharge the exhaust gas to the outside of the vehicle.
The EGR device is mounted on the exhaust pipe and the exhaust gas discharged in the engine passes through the EGR device. Further, the EGR device is connected to the intake manifold to control a combustion temperature by mixing a part of the exhaust gas with the air. The combustion temperature may be adjusted by controlling of the on and off state of an EGR valve (not illustrated) provided in the EGR device. That is, an amount of the exhaust gas supplied to the intake manifold is adjusted by controlling an on and off state of the EGR valve.
The exhaust device may further include a particulate filter that is mounted on the exhaust pipe configured to collect a particulate material contained in the exhaust gas. The particulate filter may be a device for purifying exhaust gas according to the exemplary embodiment of the present invention for purifying a harmful material other than the particulate material contained in the exhaust gas.
Hereinafter, the device for purifying exhaust gas according to the exemplary embodiment of the present invention will be described in detail with reference to the accompanying drawings.
Referring to
The engine 100 configured to generate the driving torque by a combustion of fuel may include a gasoline engine, but the present invention is not limited thereto.
As shown in
The warm-up catalytic converter 110 may be directly connected with exhaust manifold 102, and the under floor catalytic converter 130 may be separated from an exhaust manifold 102 and configured on a vehicle floor in the exhaust line 104.
Herein, the warm-up catalytic converter 110 or the under floor catalytic converter 130 includes a three-way catalyst (TWC) converting toxic materials including a carbon monoxide, a hydrocarbon, and a nitrogen oxide included in the exhaust gas into harmless substances by an oxidation and reduction reaction.
The catalyst device 120 reduces the nitrogen oxide of the exhaust gas which passes through the warm-up catalytic converter 110.
For example, the catalyst device 120 includes a selective catalyst reduction (SCR) according to an exemplary embodiment of the present invention. The catalyst device 120 is configured to inject a reducing agent such as urea into an exhaust pipe, and reduce nitrogen oxide in the exhaust gas into nitrogen and oxygen.
The selective catalytic reduction catalyst may include a Passive SCR (pSCR) of using NH3 exhausted from the LNT catalyst without a urea injection.
In addition, the catalyst device 120 may be a SGPF (SCR on GPF) coated with a selective catalyst reduction (SCR) on a gasoline particulate filter (GPF) according to another exemplary embodiment of the present invention.
The catalyst device 120 may include a LTA zeolite catalyst according to an exemplary embodiment of the present invention. A ratio of copper and aluminum of the LTA zeolite catalyst may be 11 to 16. In addition, the content of copper may be 0.5 wt % to 5 wt % with respect to the entire weight of the LTA zeolite catalyst. The content of copper may be 2 wt % to 3 wt % with respect to the entire weight of the LTA zeolite catalyst.
Hereinafter, a process of manufacturing the LTA zeolite catalyst according to the exemplary embodiment of the present invention will be described.
A method for manufacturing the catalyst according to an exemplary embodiment of the present invention includes preparing LTA zeolite having a Si/Al ratio of more than 1, preparing LTA zeolite containing ions by substituting ions in the LTA zeolite for ions, and preparing copper type LTA zeolite by performing copper (Cu) ion exchange of the LTA zeolite containing ions, and a ratio of copper and aluminum is 0.14 to 0.58. However, the present invention is not limited thereto and a ratio of active metal and aluminum may be adjusted according to a use environment of the catalyst.
First, the preparing of the LTA zeolite will be described. The LTA zeolite may be prepared by using a seed and also prepared without using the seed. A Si/Al ratio of the LTA zeolite prepared in the present process may be more than 1. More particularly, the Si/Al ratio may be 5 to 50. The Si/Al ratio may be 5 to 30. The Si/Al ratio may be 8 or more.
As an example, the process of preparing the LTA zeolite by using the seed will be described.
To prepare the LTA zeolite, first, the LTA zeolite may be prepared by mixing an LTA seed with a mixture of aluminum hydroxide (Al(OH)3) and tetraethyl orthosilicate (Si(OC2H5)4).
Particularly, a first mixture is prepared by mixing a 1,2-dimethyl-3-(4-methylbenzyl)imidazolium hydroxide aqueous solution and aluminum hydroxide (Al(OH)3) and performing primary stirring, and additionally mixing tetramethylammonium hydroxide pentahydrate and performing secondary stirring.
Herein, the first mixture may be prepared by mixing 20 wt % to 35 wt % of 1,2-dimethyl-3-(4-methylbenzyl)imidazolium hydroxide, 1 wt % to 2 wt % of aluminum hydroxide, 1 wt % to 5 wt % of tetramethylammonium hydroxide pentahydrate, and a residue amount of water with respect to a total weight of the first mixture, and the primary stirring and the secondary stirring may be performed for 0.5 hr to 1.5 hrs.
A second mixture is prepared by mixing tetraethyl orthosilicate (Si(OC2H5)4; TEOS) with the prepared first mixture and performing tertiary stirring and then mixing a LTA seed and performing quaternary stirring.
The tetraethyl orthosilicate (TEOS) may be mixed with 30 wt % to 35 wt % with respect to a total weight of the second mixture may be mixed and the LTA seed may be mixed with 2 wt % to 6 wt % with respect to a total weight of all silicon ingredients included in the LTA zeolite.
Further, the tertiary stirring may be performed for 2 hrs to 4 hrs and the quaternary stirring may be performed for 20 hrs to 28 hrs.
Thereafter, a third mixture is prepared by sufficiently heating the second mixture to evaporate ethanol and water generated due to hydrolysis of tetraethyl orthosilicate (TEOS).
The heating of the second mixture may be performed at a temperature of 70° C. to 90° C.
Thereafter, a fourth mixture is prepared by mixing a hydrogen fluoride (HF) aqueous solution with the third mixture and performing heating, washing, and drying processes.
Herein, the heating of the third mixture may be performed at a temperature of 150° C. to 200° C. for a predetermined time and the washing may be performed several times, and the drying may be performed at room temperature.
Next, the LTA zeolite for preparing the zeolite catalyst according to the exemplary embodiment of the present invention is prepared by performing additional heat treatment for removing an organic material of the fourth mixture.
The additional heat treatment may be performed at 500° C. to 700° C. for 6 hrs to 10 hrs and in the LTA zeolite according to the exemplary embodiment, the Si/Al ratio may be 5 to 50.
Further, in the case of preparing the LTA zeolite without the seed, the LTA zeolite may be prepared by the following method. 0.0 mole to 0.2 mole of aluminum hydroxide and 0.0 mole to 0.2 mole of tetramethylammonium hydroxide (hereinafter, TMAOH) are added with 0.1 mole to 1.0 mole of 1,2-dimethyl-3-(4-methylbenzyl)imidazolium hydroxide (hereinafter, 12DM3 (4 MB)IOH) as an organic structure-induced molecule and sufficiently stirred in a plastic beaker. Next, tetraethyl orthosilicate (hereinafter, TEOS) is added to have a ratio of 1 mole with respect to the reactants and sufficiently stirred again.
Next, the solution is sufficiently heated at 60° C. to 100° C. until water becomes 0 mole to 10 moles while completely removing ethanol generated due to the hydrolysis of TEOS added to the solution. Finally, 0.1 mole to 1.0 mole of hydrogen fluoride (HF) is added and sufficiently mixed to obtain a reaction mixture having a desired composition.
The reaction mixture is transferred to a Teflon reactor and put in a container made of stainless steel again, heated at 100° C. to 200° C. for 0.1 days to 14 days to prepare the LTA zeolite. Even in the LTA zeolite prepared by the method, the Si/Al ratio may be 5 to 50. However, the preparing method is exemplified and is not limited by the aforementioned method.
Next, a process of preparing the LTA zeolite containing ions by using the prepared LTA zeolite will be described in detail.
First, the LTA zeolite is put into an ammonium salt, refluxed, washed, and dried to prepare an NH4 type LTA zeolite containing NH4+ ions.
Herein, the ammonium salt may be ammonium nitrate (NH4NO3).
The refluxing process may be performed at a temperature of 60 to 100° C. for 5 hrs to 7 hrs.
In the exemplary embodiment, the ions exemplify ammonium ions, but are not limited thereto. That is, a use of other ions or ionic salts is also included in the range of the present invention.
Next, a process of preparing the copper type LTA zeolite by performing copper (Cu) ion exchange in the LTA zeolite containing ions will be described. In the copper type LTA zeolite prepared in the process, a ratio of copper and aluminum may be 0.14 to 0.58. The ratio is 0.32 to 0.48.
However, the present invention is not limited to the ratio and the ratio of copper and aluminum may be 0.1 to 0.7. The ratio of copper and aluminum may be properly adjusted according to an environmental condition to use the catalyst.
Further, when the content of copper is represented by wt %, the content of copper may be 0.5 wt % to 5 wt %. Further, the content of copper may be 2.0 wt % to 3.0 wt %.
In the above process, copper type LTA zeolite containing Cu ions may be prepared through copper (Cu) ion exchange of NH4 type LTA zeolite containing dried NH4+ ions after preparing.
The copper ion exchange is put in a copper precursor solution such as copper acetate monohydrate, copper nitride, copper nitrate, and copper sulfate and stirring is performed, and then washing and drying processes are performed to prepare the copper type LTA zeolite.
Next, the copper type LTA zeolite may be heat-treated after gradually increasing the temperature in an oven to prepare the catalyst according to the exemplary embodiment of the present invention.
Herein, the heat treatment of the copper type LTA zeolite may be performed for 1 hr to 24 hrs after increasing the temperature up to 400° C. to 750° C. at PC/min to 30° C./min.
In the copper type LTA zeolite prepared in the process, a ratio of copper and aluminum may be 0.14 to 0.58. The ratio of copper and aluminum may be 0.32 to 0.48.
The ratio of copper and aluminum is a ratio having thermal stability and excellent NOx purification performance.
As a result, in the device for purifying exhaust gas according to the exemplary embodiment of the present invention, the Cu/LTA catalyst with improved high-temperature performance is applied the SCR or the SGPF, thereby increasing the heat resistance of the catalyst and improving the nitrogen oxide purification performance in a gasoline engine.
Referring to
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As such, in the device for purifying exhaust gas according to an exemplary embodiment of the present invention, the LTA zeolite catalyst with an improved high-temperature performance is applied the SCR or the SGPF, and thus it is possible to provide an environment that can increase heat resistance of the catalyst in the gasoline engine, improve the nitrogen oxide purification performance, and improve fuel economy.
For convenience in explanation and accurate definition in the appended claims, the terms “upper”, “lower”, “inner”, “outer”, “up”, “down”, “upwards”, “downwards”, “front”, “rear”, “back”, “inside”, “outside”, “inwardly”, “outwardly”, “interior”, “exterior”, “forwards”, and “backwards” are used to describe features of the exemplary embodiments with reference to the positions of such features as displayed in the figures.
The foregoing descriptions of specific exemplary embodiments of the present invention have been presented for purpose of illustration and description. They are not intended to be exhaustive or to limit the invention to the precise forms disclosed, and obviously many modifications and variations are possible in light of the above teachings. The exemplary embodiments were chosen and described in order to explain certain principles of the invention and their practical application, to thereby enable others skilled in the art to make and utilize various exemplary embodiments of the present invention, as well as various alternatives and modifications thereof. It is intended that the scope of the invention be defined by the Claims appended hereto and their equivalents.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2016-0159258 | Nov 2016 | KR | national |
