Patent Application
20220134321
This application claims priority to and the benefit of Korean Patent Application No. 10-2020-0146180 filed in the Korean Intellectual Property Office on Nov. 4, 2020, the entire contents of which are incorporated herein by reference.
The present disclosure relates to a method of preparing an SCR catalyst and an SCR catalyst prepared thereby, and more particularly, to a method of preparing an SCR catalyst having improved thermal durability and NOx purification performance, and an SCR catalyst prepared thereby.
Zeolite is a porous material that fine pores with unique and regular shapes and sizes are well developed.
Acidity of the zeolite may be controlled within a wide range by varying an amount of aluminum present in the skeleton and zeolite has a large specific surface area and may exchange cations, and therefore the zeolite is widely used as a catalyst or an adsorbent in the field of fine chemistry.
Recently, a selective catalytic reduction (SCR) reaction has been commercialized in a post-treatment device for removing nitrogen oxides from automobile exhaust gas according to environmental regulations. As a catalyst for the reaction, copper ion-exchanged Cu/CHA exhibits high activity over a wide temperature range and excellent hydrothermal stability, compared with other zeolites, and thus draws a great interest.
In addition, recently, a technology of coating the SCR catalyst on a diesel particulate filter (DPF) to increase NOx purification performance has been developed, but in order to apply the SCR catalyst to DPF, a catalyst having higher thermal durability and excellent NOx purification performance is required. However, when the aluminum present in the zeolite skeleton is exposed to hot water vapor, the aluminum may be eluted out of the skeleton and thus the structure of the zeolite may collapse, resulting in deteriorating catalytic activity. In addition, since various types of cations present in the zeolite also affect hydrothermal stability, the contents of these components should be controlled in order to increase the hydrothermal stability of the zeolite.
An object of the present disclosure is to provide a method of preparing an SCR catalyst having a Si/Al mole ratio of greater than or equal to about 15, maintaining a zeolite structure even after degradation, and having excellent thermal durability and NOx purification performance.
Another object of the present disclosure is to provide an SCR catalyst prepared by the above preparation method.
According to an embodiment of the present disclosure, a method of preparing a SCR (Selective Catalytic Reduction) catalyst includes preparing a synthetic mother liquid that includes a source of silica and alumina including zeolite A and silica, a structure-inducing material, a complexing material, and a solvent, reacting the synthetic mother liquid to prepare CHA zeolite, and ion-exchanging the prepared CHA zeolite with a transition metal.
The zeolite A may be an NH4-exchanged zeolite A.
The silica may be fumed silica or colloidal silica.
The structure-inducing material may include trimethyladamantyl ammonium hydroxide (AdaOH), benzyl trimethyl ammonium hydroxide, benzyl trimethyl ammonium chloride, choline chloride, or a combination thereof.
The complexing material may be an alkali hydroxide solution including sodium hydroxide.
The synthetic mother liquid may include about 5 mol % to about 30 mol % of the zeolite A and about 70 mol % to about 95 mol % of the silica based on a total amount of the source of silica and alumina.
The synthetic mother liquid may include about 0.1 parts by mole to about 0.4 parts by mole of the structure-inducing material and about 0.1 parts by mole to about 0.4 parts by mole of the complexing material based on 1 part by mole of the source of silica and alumina.
In the second process, the reaction may be performed under conditions of about 120° C. to about 140° C., about 2 days to about 6 days, and about 0 rpm to about 60 rpm.
In the second process, after the reaction, the method may further include firing at about 500° C. to about 600° C. for 4 to 12 hours.
The CHA zeolite prepared in the second process may have a Si/Al mole ratio of about 15 to about 30.
The transition metal may include Cu, Fe, Co, Ti, Zn, Ag, Mn, or a combination thereof.
The SCR catalyst may include about 1 wt % to about 5 wt % of the transition metal based on the total catalyst.
In the third process, the ion-exchanging may be performed at about 25° C. to about 80° C. for about 1 hour to about 24 hours.
According to another embodiment of the present disclosure, a SCR (Selective Catalytic Reduction) catalyst prepared by the above preparation method is provided.
The preparation method of the SCR catalyst according to the present disclosure may provide an SCR catalyst having a Si/Al mole ratio of greater than or equal to about 15 and maintaining the zeolite structure after the degradation and thus having high thermal durability and excellent NOx purification performance.
This disclosure will be described more fully hereinafter in the following detailed description, in which some but not all embodiments of this disclosure are described with reference to the attached drawings. This disclosure may be embodied in many different forms and is not be construed as limited to the embodiments set forth herein. Unless otherwise defined, all terms used in the specification (including technical and scientific terms) may be used with meanings commonly understood by a person having ordinary knowledge in the art. Further, unless explicitly defined to the contrary, the terms defined in a generally-used dictionary are not ideally or excessively interpreted.
In addition, 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.
Unless specifically described to the contrary, a singular form includes a plural form.
A method of preparing a SCR (Selective Catalytic Reduction) catalyst according to an embodiment of the present disclosure includes preparing a synthetic mother liquid that includes a source of silica and alumina including zeolite A and silica, a structure-inducing material, a complexing material, and a solvent, reacting the synthetic mother liquid to prepare CHA zeolite, and ion-exchanging the prepared CHA zeolite with a transition metal.
First, synthetic mother liquid including a source of silica and alumina, a structure-inducing material, a complexing material, and a solvent is prepared at 51.
When the zeolite A is used as the source of silica and alumina, CHA zeolite having an Si/Al mole ratio of about 15 to about 30 may be synthesized.
The zeolite A may be NH4-exchanged zeolite A. When the zeolite A is the NH4-exchanged zeolite A, CHA zeolite having an Si/Al mole ratio of about 15 to about 30 may be synthesized.
The silica may be fumed silica or colloidal silica. When the zeolite A is reacted with the fumed silica or silica, CHA zeolite having an Si/Al mole ratio of about 15 to about 30 may be prepared.
When the CHA zeolite has an Si/Al mole ratio of less than about 15, high temperature durability may be deteriorated, and when the CHA zeolite has an Si/Al mole ratio of greater than about 30, transition metals may not be sufficiently supported.
The synthetic mother liquid may further include, for example, sodium aluminate (NaAlO2), AlCl3, Al2(SO4)3, aluminum hydroxide (Al(OH)3), kaolin, clay, zeolite, or a combination thereof as an additional alumina source. In addition, the synthetic mother liquid may further include zeolite, silicate, silica hydrogel, silicic acid, tetraalkyl orthosilicate, silica hydroxide, precipitated silica, or a combination thereof as an additional silica source.
The synthetic mother liquid may include the zeolite A in an amount of about 5 mol % to about 30 mol %, for example, about 5 mol % to about 20 mol % and the silica in an amount of about 70 mol % to about 95 mol %, for example, about 80 mol % to about 95 mol % based on a total amount of the source of silica and alumina. When the zeolite A is included in an amount of less than about 5 mol % or greater than about 30 mol %, amorphous products or impurities may be generated. When the silica is included in an amount of less than about 70 mol % or greater than about 95 mol %, likewise, the amorphous products or impurities may also be generated.
The structure-inducing material may include trimethyladamantyl ammonium hydroxide (AdaOH), benzyl trimethyl ammonium hydroxide, benzyl trimethyl ammonium chloride, choline chloride, or a combination thereof. In addition, a generally-used structure-inducing material for preparing CHA may also be included. The complexing material may be an alkali hydroxide solution including sodium hydroxide.
The synthetic mother liquid may include about 0.1 parts by mole to about 0.4 parts by mole of the structure-inducing material and about 0.1 parts by mole to about 0.4 parts by mole of the complexing material based on 1 part by mole of the source of silica and alumina. According to the amount of the complexing material added to the synthetic mother liquid, an amount of aluminum present in the synthesized CHA zeolite skeleton may vary, and thereby hydrothermal characteristics may vary.
Subsequently, the synthetic mother liquid is reacted to prepare CHA zeolite at S2.
Specifically, the synthetic mother liquid is reacted at about 120° C. to about 140° C. for about 2 days to about 6 days, while rotated at about 0 rpm to about 60 rpm and then, separated through centrifugation, washed, and fired at about 500° C. to about 600° C. for about 4 hours to about 12 hours to prepare CHA zeolite.
On the other hand, the CHA zeolite may be Na-formed CHA zeolite, and optionally, preparing NH4-formed CHA zeolite may be further included by ion-exchanging the Na-formed CHA zeolite with cations. Specifically, the Na-formed CHA zeolite is dipped in a 1.5 M ammonium nitrate aqueous solution and then, stirred at about 60° C. to about 80° C. for greater than or equal to about 3 hours, which may be three times repeated to ion-exchange it into the form of NH4+, and then, washed, dried, and fired to obtain the NH4-formed CHA zeolite.
Subsequently, the prepared CHA zeolite is ion-exchanged with a transition metal at S3.
Specifically, the ion-exchange of the CHA zeolite with transition metals may be performed using an ion-exchanging method of adding the CHA zeolite to a solution including a precursor of the transition metal to support the transition metal on the CHA zeolite.
The transition metal may include Cu, Fe, Co, Ti, Zn, Ag, Mn, or a combination thereof. The precursor of the transition metal may include nitrate, hydrochloride, acetate, or sulfate. For example, when the metal is Cu, the metal oxide precursor may be copper nitrate (II) (Cu(NO3)2) or copper acetate (Cu acetate).
The solvent may include distilled water, deionized water, ethanol, methanol, ethylene glycol, propylene glycol, isopropyl alcohol, or a combination thereof.
The ion-exchanging may be performed at about 25° C. to about 80° C. for about 1 hour to about 24 hours depending on a type of the transition metal and an amount of exchanged ions.
On the other hand, the prepared SCR catalyst may be hydrothermally treated for a hydrothermal stability test. The hydrothermal treatment may be performed for about 12 hours, while flowing air containing about 10% of water at about 100 ml/min into a catalyst layer heated at about 800° C. to about 900° C.
The SCR catalyst according to an embodiment of the present disclosure is prepared in the preparation method.
The SCR catalyst may be coated on a catalyst substrate such as a honeycomb including a wall-flow filter substrate or a through-flow substrate, and an NOx level in the exhaust gas may be reduced by contacting the SCR catalyst with the gas for sufficient time and temperature to reduce the NOx level in the gas.
Hereinafter, specific examples of the disclosure are presented. However, the examples described below are for illustrative purposes only, and the scope of the disclosure is not limited thereto.
A synthetic mother liquid was prepared with the composition shown in Table 1 below.
The synthetic mother liquid was mixed and put in an autoclave and then, reacted for 4 days, while rotated at 40 rpm at 140° C., separated through centrifugation, washed, and fired at 550° C. for 12 hours to obtain CHA zeolite (CHA-1).
The CHA zeolite was added to a 1.0 M copper acetate aqueous solution and ion-exchanged at 25° C. for 24 hours and then, washed, dried, and fired to prepare a copper ion-exchanged CHA zeolite (Cu/CHA-1).
CHA zeolite (CHA-2A) and copper ion-exchanged CHA zeolite (Cu/CHA-2A) were prepared according to the same method as the comparative example except that the synthetic mother liquid was prepared with the composition shown in Table 1.
CHA zeolite (CHA-2B) and copper ion-exchanged CHA zeolite (Cu/CHA-2B) were prepared according to the same method as the comparative example except that the synthetic mother liquid was prepared with the composition shown in Table 1.
1)SDA: trimethyladamantyl ammonium hydroxide (AdaOH)
Physicochemical characteristics of the CHA zeolites according to the comparative example and Examples 1 and 2 were measured, and the results are shown in Table 2. In addition, electron microscopic photographs of the CHA zeolites according to the comparative example and Examples 1 and 2 were respectively shown in
Referring to Table 2 and
Referring to
Referring to
After hydrothermally treating (degrading) the CHA zeolites ion-exchanged with copper according to the comparative example and Examples 1 and 2 for 12 hours, while flowing air containing 10% water at 100 ml/min into a catalyst layer heated to 900° C., performance of SCR catalysts before and after the degradation was evaluated.
Referring to
Nitrogen adsorption experiments of the SCR catalysts according to the comparative example and Examples 1 and 2 were conducted, and the results are shown in Table 3 and
1)EDX Measurement Result
Referring to Table 3 and
Referring to
While this disclosure has been described in connection with what is presently considered to be practical example embodiments, it is to be understood that the disclosure is not limited to the disclosed embodiments. On the contrary, it is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2020-0146180 | Nov 2020 | KR | national |
