Dry reforming catalyst using metal oxide support, and method for preparing synthetic gas by using same

Abstract

The present invention relates to a dry reforming catalyst in which an active material is impregnated on the surface of a metal oxide support and the active material is surrounded by a surfactant, a method of preparing the same, and a method of producing a synthetic gas using the catalyst. Since the surfactant on the surface of the active material prevents the active material from being sintered and the active material surface from being covered with carbon, the dry reforming catalyst exhibits high activity at high temperature for a long period of time without having to use a precious metal, and thus is useful for the production of a synthetic gas.

Claims

1. A dry reforming catalyst in which an active material is impregnated on a surface of a metal oxide support and the active material is surrounded by a surfactant, wherein the weight ratio of the active material: the metal oxide support: the surfactant is 0.01 to 40:59.6 to 99.5:0.04; the metal oxide is one or more selected from the group consisting of MgO, TiO.sub.2, Al.sub.2O.sub.3, SiO.sub.2, CrO.sub.2, Fe.sub.2O.sub.3, Fe.sub.3O.sub.4, CuO, ZnO, CaO, Sb.sub.2O.sub.4, Co.sub.3O.sub.4, Pb.sub.3O.sub.4, Mn.sub.3O.sub.4, Ag.sub.2O.sub.2, U.sub.3O.sub.8, Cu.sub.2O, Li.sub.2O, Rb.sub.2O, Ag.sub.2O, Tl.sub.2O, BeO, CdO, TiO, GeO.sub.2, HfO.sub.2, PbO.sub.2, MnO.sub.2, TeO.sub.2, SnO.sub.2, La.sub.2O.sub.3, CeO.sub.2, WO.sub.2, UO.sub.2, ThO.sub.2, TeO.sub.2 and MoO.sub.3; the active material is one or more selected from the group consisting of nickel (Ni), cobalt Co), ruthenium (Ru), palladium (Pd), iridium (Ir), platinum (Pt), rhodium (Rh) and molybdenum carbide (Mo.sub.2C); the active material further comprises a promoter; and the promoter is Molybdenum (Mo).

2. The dry reforming catalyst of claim 1, wherein the dry reforming catalyst has a pore area of greater than 0 to 5,000 m.sup.2/g and a CO.sub.2 and CH.sub.4 conversion of 95 to 98%.

3. The dry reforming catalyst of claim 1, wherein the catalyst is used for the dry reforming reaction of methane.

4. A method of preparing a dry reforming catalyst of claim 1, comprising: (a) obtaining a mixture by dissolving an active material precursor, a metal oxide support and a surfactant in a polyol solvent; and (b) preparing a catalyst in which the active material is impregnated on the surface of the metal oxide support by adding a reducing agent to the mixture.

5. The method of preparing a dry reforming catalyst of claim 4, wherein the active material is nickel (Ni).

6. The method of preparing a dry reforming catalyst of claim 4, wherein a precursor of nickel is one or more selected from the group consisting of NiCl.sub.2, NiCl.sub.2.6H.sub.2O, Ni(NO.sub.3).sub.2, NiSO.sub.4, (NH.sub.4).sub.2Ni(SO.sub.4).sub.2.6H.sub.2O, Ni(OCOCH.sub.3).sub.2.4H.sub.2O, NiBr.sub.2, NiCO.sub.3, NiF.sub.2, NiI.sub.2, NiC.sub.2O.sub.4.2H.sub.2O, and Ni(ClO.sub.4).sub.2.6H.sub.2O.

7. The method of preparing a dry reforming catalyst of claim 4, wherein the surfactant is one or more selected from the group consisting of polyvinylpyrrolidone (PVP), oleylamine, oleic acid, benzyl ether, trioctylphosphine, octadecylamine, hexadecylamine, cetyl trimethylammonium bromide (CTAB), polyethyleneglycol (PEG), 1,2-hexadecanediol and 1-octadecene.

8. The method of preparing a dry reforming catalyst of claim 4, wherein the reducing agent is one or more selected from the group consisting of hydrazine, NaBH.sub.4, LiAlH.sub.4, diisobutylaluminum hydride (DIBAL-H) and diborane.

9. A method of dry reforming methane, the method comprises producing a synthetic gas composed of hydrogen and carbon monoxide by reacting methane with carbon dioxide at 600 to 800° C. in the presence of the dry reforming catalyst of claim 1.

10. The method of dry reforming methane of claim 9 wherein the method is performed at a pressure of 1 to 30 bar.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a transmission electron microscope (TEM) image of a catalyst prepared in Example of the present invention.

(2) FIG. 2 is a schematic view of a dry reforming catalyst according to the present invention.

(3) FIG. 3 is a schematic view of a catalyst prepared in Example 1 of the present invention.

(4) FIG. 4 is an X-ray diffraction image of a catalyst prepared in Example 1 of the present invention.

(5) FIG. 5 is a nitrogen adsorption curve of a catalyst prepared in Example 1 of the present invention.

(6) FIG. 6 shows the results of measuring the temperature-dependent reaction activity of a catalyst prepared in Example 1.

(7) FIG. 7 shows the results of measuring the temperature-dependent conversion rate of a catalyst prepared in Example 1.

(8) FIG. 8 shows the results of measuring the time-dependent stability of a catalyst prepared in Example 1.

BEST MODE FOR CARRYING OUT THE INVENTION

(9) Unless defined otherwise, all the technical and scientific terms used herein have the same meaning as those generally understood by one of ordinary skill in the art to which the invention pertains. Generally, the nomenclature used herein and the experiment methods, which will be described below, are those well-known and commonly employed in the art.

(10) In the present invention, it could be confirmed that a catalyst showing no decrease in activity could be prepared by a novel method instead of a general catalyst synthesis method such as wet impregnation, calcination or reduction, and that when a dry reforming catalyst was prepared in which an active material is impregnated on the surface of a metal oxide support and the active material is surrounded by a surfactant, the surfactant on the surface of the active material prevented the active material from being sintered and the active material surface from being covered with carbon, so that the dry reforming catalyst could exhibit high activity at high temperature for a long period of time without having to use a precious metal.

(11) Therefore, in one aspect, the present invention is directed to a dry reforming catalyst in which an active material is impregnated on the surface of a metal oxide support and the active material is surrounded by a surfactant. The dry reforming catalyst according to the present invention is schematically shown in FIG. 2.

(12) In another aspect, the present invention is directed to a method of preparing a dry reforming catalyst, comprising: (a) obtaining a mixture by dissolving an active material precursor, a metal oxide support and a surfactant in a polyol solvent; and

(13) (b) preparing a catalyst in which the active material is impregnated on the surface of the metal oxide support by adding a reducing agent to the mixture.

(14) In the present invention, the metal oxide may be one or more selected from the group consisting of ZrO.sub.2, MgO, TiO.sub.2, Al.sub.2O.sub.3, SiO.sub.2, CrO.sub.2, Fe.sub.2O.sub.3, Fe.sub.3O.sub.4, CuO, ZnO, CaO, Sb.sub.2O.sub.4, Co.sub.3O.sub.4, Fe.sub.3O.sub.4, Pb.sub.3O.sub.4, Mn.sub.3O.sub.4, Ag.sub.2O.sub.2, U.sub.3O.sub.8, Cu.sub.2O, Li.sub.2O, Rb.sub.2O, Ag.sub.2O, Tl.sub.2O, BeO, CdO, TiO, GeO.sub.2, HfO.sub.2, PbO.sub.2, MnO.sub.2, TeO.sub.2, SnO.sub.2, La.sub.2O.sub.3, Fe.sub.2O.sub.3, CeO.sub.2, WO.sub.2, UO.sub.2, ThO.sub.2, TeO.sub.2 and MoO.sub.3, and SiO.sub.2, Al.sub.2O.sub.3, MgO, CeO.sub.2 or La.sub.2O.sub.3 is preferably used as the metal oxide, but is not limited thereto.

(15) In addition, the active material may be one or more selected from the group consisting of an active metal such as nickel (Ni), cobalt (Co), ruthenium (Ru), palladium (Pd), iridium (Ir), platinum (Pt), and rhodium (Rh), and molybdenum carbide (Mo.sub.2C).

(16) The active material may further comprise a promoter such as molybdenum (Mo). Molybdenum (Mo) itself does not exhibit activity, but acts as a promoter that facilitates the distribution of the active material or change the energy state of the active material to further improve the efficiency of the catalyst. Preferably, nickel (Ni) and/or molybdenum (Mo) is used as the active material, but is not limited thereto.

(17) In addition, the surfactant may be one or more selected from the group consisting of polyvinylpyrrolidone (PVP), oleylamine, oleic acid, benzyl ether, trioctylphosphine, octadecylamine, hexadecylamine, cetyl trimethylammonium bromide (CTAB), polyethyleneglycol (PEG), 1,2-hexadecanediol, and 1-octadecene. Preferably, polyvinylpyrrolidone (PVP) is used as the surfactant, but is not limited thereto.

(18) The reducing agent used in the method of preparing the dry reforming catalyst of the present invention may be one or more selected from the group consisting of hydrazine, NaBH.sub.4, LiAlH.sub.4, diisobutylaluminum hydride (DIBAL-H), and diborane. Preferably, hydrazine is used as the reducing agent, but is not limited thereto.

(19) The polyol solvent used in the method of preparing the dry reforming catalyst of the present invention may be one or more selected from the group consisting of ethylene glycol (EG), diethylene glycol (DEG), triethylene glycol (TrEG), polyethylene glycol (PEG), propanediol (PDO), butanediol (BD), pentanediol (PD), glycerol (GLY), and pentaerythritol (PE).

(20) The weight ratio of the active material:the magnesium oxide support: the surfactant may be 0.01 to 40:59.6 to 99.5:0.04. In this range, the catalyst advantageously has high activity and long-lasting stability, and when the weight ratio is out of this range, a problem arises in that the activity of the catalyst readily decreases as the reaction progresses.

(21) According to one preferred embodiment of the present invention, there is provided a nickel-molybdenum dry reforming catalyst in which nickel and molybdenum are impregnated on the surface of a magnesium oxide support and the nickel is surrounded by a surfactant, the catalyst having a nickel content of 0.01 to 100 wt % and a molybdenum content of 99.9 to 0 wt %. The nickel-molybdenum dry reforming catalyst according to the present invention is schematically shown in FIG. 3.

(22) Furthermore, the catalyst according to the present invention may have a formula of Ni.sub.10Mo.sub.2@MgO.

(23) A precursor of nickel in the method of preparing the nickel-molybdenum dry reforming catalyst of the present invention may be one or more selected from the group consisting of NiCl.sub.2, NiCl.sub.2.6H.sub.2O, Ni(NO.sub.3).sub.2, NiSO.sub.4, (NH.sub.4).sub.2Ni(SO.sub.4).sub.2.6H.sub.2O, Ni(OCOCH.sub.3).sub.2.4H.sub.2O, NiBr.sub.2, NiCO.sub.3, NiF.sub.2, NiI.sub.2, NiC.sub.2O.sub.4.2H.sub.2O, and Ni(CLO.sub.4).sub.2.6H.sub.2O, and a precursor of molybdenum may be one or more selected from the group consisting of Mo(CO).sub.6, MoO.sub.3, Na.sub.2MoO.sub.4, CaMoO.sub.4, ZnMoO.sub.4, and (NH.sub.4).sub.6Mo.sub.7O.sub.24.4H.sub.2O.

(24) The prepared dry reforming catalyst may have a pore area of 0 to 5,000 m.sup.2/g, preferably 10 to 3,000 m.sup.2/g, and a conversion of 95 to 98%, and may be used for the dry reforming reaction of methane. Within the range of the pore area, the active metal may be supported. The larger the pore area, the more active material may be supported.

(25) In still another aspect, the present invention is directed to a method for dry reforming of methane, comprising producing a synthetic gas composed of hydrogen and carbon monoxide by reacting methane with carbon dioxide at 600 to 800° C. in the presence of the dry reforming catalyst.

(26) The method for dry reforming of the methane may be performed at a high pressure of 1 to 30 bar, preferably 1 to 20 bar, more preferably 1 to 16 bar.

EXAMPLES

(27) Hereinafter, the present invention will be described in further detail with reference to examples. It will be obvious to a person having ordinary skill in the art that these examples are for illustrative purposes only and are not to be construed to limit the scope of the present invention.

Example 1: Preparation of Ni.SUB.10.Mo.SUB.2.@MgO Catalyst

(28) Ethylene glycol (Samchun Chemicals), nickel chloride hydrate (NiCl.sub.26H.sub.2O, Samchun Chemicals), ammonium heptamolybdate tetrahydrate (NH.sub.4).sub.6Mo.sub.7O.sub.24.4H.sub.2O, Samchun Chemicals) and polyvinylpyrrolidone (Sigma-Aldrich) were used. NaOH (Samchun Chemicals), hydrazine (Sigma Aldrich) and magnesium oxide were used as dry ice and magnesium metal.

(29) First, 0.404 g of a nickel precursor and 36 mg of a molybdenum precursor were dissolved in 1 mL of water and 24 mL of ethylene glycol, and then 0.38 g of PVP was added thereto, followed by stirring. 0.9 g of magnesium oxide was added to the solution which was then stirred, after which the temperature of the solution was increased to 80° C. To the solution, a hydrazine solution (1.7 g of hydrazine/5 mL of ethylene glycol) was added, and when the solution changed color, a solution of 136 mg of NaOH in 10 mL of ethylene glycol was added. As the color of the solution gradually became black, nickel and molybdenum ions were reduced and impregnated on the surface of the magnesium oxide. After 1 hour of stirring, the solution was washed with water and dried, thereby obtaining a catalyst.

Example 2: Characterization of Reaction for Producing Synthetic Gas Using Catalyst

(30) The synthesized catalyst was analyzed by TEM, and as a result, it was confirmed that nickel and molybdenum were distributed uniformly on the surface of the magnesium oxide and that the active material metal nickel was surrounded by the surfactant PVP.

(31) FIG. 4 shows the results of measuring X-ray diffraction. As shown in FIG. 4, Ni and MgO were found. The concentration of Ni was relatively low, and thus the intensity of the peak was relatively weaker than that of MgO. Mo was not detected in the results of XRD due to its low concentration. To determine the exact metal contents, the elements contained in the catalyst were analyzed by ICP and elemental analysis. As a result, as shown in Table 1 below, it was confirmed that the content of nickel was 7.09% and the content of molybdenum was 1.55%. In addition, PVP used as the surfactant covered the surface of the active material, and thus the detected contents of carbon and nitrogen were 4.42% and 0.15%, respectively. To measure the porosity, the catalyst was adsorbed with liquid nitrogen at 77K, and the adsorbed quantity of the liquid nitrogen was measured. As a result, it was shown that the porosity of the catalyst was not high (20 m.sup.2/g), but the activity of the catalyst was high (FIG. 5).

(32) In order to examine the effect of temperature on the catalyst, 50 mg of the synthesized catalyst was placed in a quartz tube reactor, and the temperature-dependent activity of the catalyst was measured while changing the reaction temperature (FIG. 6). The operating temperature was 600 to 800° C. The composition of reactants was CO.sub.2:CH.sub.4:He=1:1:8, and the flow rate was 50 mL/min. The weight hourly space velocity (WHSV) was 60 L/g.sub.cath. The conversion was measured by gas chromatography (Simadzu, GC Tracera). As shown in FIG. 6, the conversion increased with increasing temperature, and the catalyst showed a CO.sub.2 conversion of 95% and a CH.sub.4 conversion of 98% at 800° C.

(33) As shown in FIG. 7, it could be seen that the H.sub.2/CO ratio of the product increased with increasing temperature and reached 0.96, which approaches a theoretical value of 1, at 800° C.

(34) In order to examine the stability of the catalyst during a reaction, the time-dependent conversion of the reactants was measured at a high temperature of 800° C. (FIG. 8). 100 mg of the catalyst was used for a reactant composition of CO.sub.2:CH.sub.4:He=1:1:8 at a flow rate of 20 mL/min, and the conversion rate of the reactants was measured. The WHSV was 12 L/g.sub.cath. As a result, the catalyst showed constant performance without a change in the conversion rate for 65 hours. The results obtained after 65 hours are not significantly different from the results of the first measurement, suggesting that the catalyst is stable even when it is used in the reaction for 65 hours or more.

(35) TABLE-US-00001 TABLE 1 Ni Mo Mg C N H O Ni.sub.10Mo.sub.2@MgO 7.09% 1.55% 40.22% 4.42% 0.15% 1.51% 31%

(36) In addition, in order to examine the stability of the catalyst during a reaction at high pressure, the conversion rate of reactants was measured at a pressure of 1 to 16 bar (Table 2). 3.7 g of the catalyst was used under the condition of CO.sub.2:CH.sub.4:He=41.66 mL/min:41.66 mL/min:16.68 mL/min, and the conversion rate of the reactants was measured. It was confirmed that when methane and carbon dioxide were reacted at high pressure in the presence of the dry reforming catalyst, they could be converted to a synthetic gas composed of hydrogen and carbon monoxide.

(37) TABLE-US-00002 TABLE 2 Tem- 780~850 780~850 780~850 780~850 800~850 800~850 800~850 800~850 800~850 800~850 800~850 800~850 pera- ture (° C.) Pres- 1 3 3 10 10 10 10 10 10 10 10 16 sure (bar) CH.sub.4 29.39 7.09 ~0.5 5.6 7.99 8.03 10.39 9.75 9.56 11.53 11.47 7.23 N.sub.2 14.5 14.17 14.49 15.06 16.02 15.84 16.87 16.5 16.46 17.44 17.88 20.53 CO.sub.2 26.29 10.68 11.16 22.25 24.2 23.56 28.14 27.13 26.27 29.54 31.52 36.84 CO 18.81 38.71 41.36 37.52 34.3 35.68 29.09 31.32 32.24 27.72 26.77 25.97 H.sub.2 10.98 29.33 32.97 19.54 17.47 16.88 15.5 15.25 14.98 13.74 12.34 9.42

INDUSTRIAL APPLICABILITY

(38) The dry reforming catalyst according to the present invention can be prepared by a novel method instead of a general catalyst synthesis method such as wet impregnation, calcination or reduction, in which a catalyst shows no activity. In addition, the surfactant on the surface of the active material prevents the active material from being sintered and the active material surface from being covered with carbon, so that the dry reforming catalyst can exhibit high activity at high temperature and pressure for a long period of time even without having to use a precious metal, and thus, it can be as a catalyst for the dry reforming reaction. In addition, the dry reforming catalyst is useful for the production of a high value-added chemical substance, because the ratio of hydrogen to carbon monoxide in the product is about 1:1.

(39) Although the present invention has been described in detail with reference to the specific features, it will be apparent to those skilled in the art that this description is only for a preferred embodiment and does not limit the scope of the present invention. Thus, the substantial scope of the present invention will be defined by the appended claims and equivalents thereof.