ADSORBENT FOR CAPTURING CARBON DIOXIDE COMPRISING MAGNESIUM OXIDE/TITANIUM DIOXIDE COMPOSITE AND METHOD FOR MANUFACTURING SAME

Abstract

Provided is an adsorbent for capturing carbon dioxide and a method for manufacturing same, and more particularly, to an adsorbent for capturing carbon dioxide, including a magnesium oxide/titanium dioxide composite having wide surface area, large pore volume and good CO.sub.2 adsorption performance, and a method for manufacturing same. According to the present invention, a novel MgO based composite metal oxide which may stably adsorb CO.sub.2 at a low temperature such as room temperature is provided. The adsorbent for capturing carbon dioxide, including a magnesium oxide/titanium dioxide composite has good thermal stability, and controls basic sites easily, and is used in various fields for capturing carbon dioxide. In addition, by controlling the molar ratio of the metal ions of the magnesium oxide/titanium dioxide composite and controlling morphology, an adsorbent for capturing carbon dioxide having large surface area and pore volume and strong basic sites may be provided.

Claims

1. An adsorbent for capturing carbon dioxide comprising a magnesium oxide/titanium dioxide composite.

2. The adsorbent for capturing carbon dioxide according to claim 1, wherein the magnesium oxide/titanium dioxide composite has a mesoporous structure.

3. The adsorbent for capturing carbon dioxide according to claim 1, wherein the magnesium oxide/titanium dioxide composite is formed by self-assembly of a metal precursor comprising a magnesium precursor and a titanium precursor with a soft template.

4. The adsorbent for capturing carbon dioxide according to claim 3, wherein the magnesium precursor is magnesium nitrate hexahydrate or magnesium acetate tetrahydrate, and the titanium precursor is titanium isopropoxide or titanium tetrabutoxide.

5. The adsorbent for capturing carbon dioxide according to claim 3, wherein the soft template is diblock copolymer or triblock copolymer.

6. The adsorbent for capturing carbon dioxide according to claim 5, wherein the triblock copolymer is polyethylene glycol-polypropylene glycol-polyethylene glycol or cetrimonium bromide.

7. The adsorbent for capturing carbon dioxide according to claim 1, wherein the molar ratio of magnesium/titanium is greater than 2.0 and less than 5.0.

8. The adsorbent for capturing carbon dioxide according to claim 1, wherein the molar ratio of magnesium/titanium is from 3.0 to 4.0.

9. The adsorbent for capturing carbon dioxide according to claim 1, wherein the magnesium oxide/titanium dioxide composite has a crystalline phase of MgTi.sub.2O.sub.4.

10. A method for manufacturing an adsorbent for capturing carbon dioxide comprises: dissolving a surfactant in a solvent; adding a metal precursor comprising a magnesium precursor and a titanium precursor and an acid in the solvent, and stirring; evaporating the solvent to obtain a self-assembled solid of the metal precursor and the surfactant; and calcining the solid at a temperature of 500° C. or more to remove the surfactant.

11. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 10, wherein the magnesium precursor is magnesium nitrate hexahydrate or magnesium acetate tetrahydrate, and the titanium precursor is titanium isopropoxide or titanium tetrabutoxide.

12. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 10, wherein the solvent is selected from ethanol, methanol, isopropyl alcohol and a combination thereof.

13. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 10, wherein the surfactant is a soft template.

14. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 13, wherein the soft template is diblock copolymer or triblock copolymer.

15. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 14, wherein the triblock copolymer is polyethylene glycol-polypropylene glycol-polyethylene glycol or cetrimonium bromide.

16. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 10, wherein the acid is selected from nitric acid, acetic acid, hydrochloric acid, sulfuric acid and a combination thereof.

17. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 10, wherein the magnesium precursor and the titanium precursor are added so that the molar ratio of magnesium/titanium is greater than 2.0 and less than 5.0.

18. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 10, wherein the magnesium precursor and the titanium precursor are added so that the molar ratio of magnesium/titanium is from 3.0 to 4.0.

19. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 10, wherein the stirring is performed for 4 to 10 hours.

20. The method for manufacturing an adsorbent for capturing carbon dioxide according to claim 10, wherein calcining is performed for 4 to 10 hours.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0026] FIG. 1 illustrates a manufacturing process of an adsorbent for capturing carbon dioxide comprising a magnesium oxide/titanium dioxide composite according to an embodiment of the present invention;

[0027] FIG. 2 illustrates thermogravimetric analysis results of 3MgO—TiO.sub.2 adsorbents according to example 1 and example 2 of the present invention;

[0028] FIG. 3(a) is N.sub.2 adsorption-desorption isotherm curves of xMgO-TiO.sub.2 according to example 1 of the present invention;

[0029] FIG. 3(b) is pore size distribution curves of xMgO-TiO.sub.2 according to example 1 of the present invention;

[0030] FIG. 4 illustrates analysis results of X-ray diffraction (XRD) patterns of xMgO-TiO.sub.2 according to example 1 of the present invention;

[0031] FIG. 5 show images wherein (a) to (c) are field emission transmission electron microscope (FE-TEM) images of 3MgO—TiO.sub.2 according to example 1 of the present invention; (d) is an field emission scanning electron microscope (FE-SEM) image of 3MgO—TiO.sub.2 according to example 1 of the present invention; and (e) to (h) are energy dispersive spectroscopy (EDS)-elemental mapping images of 3MgO—TiO.sub.2 according to example 1 of the present invention;

[0032] FIG. 6(a) illustrates CO.sub.2 adsorption curves at 25° C. of xMgO-TiO.sub.2 according to example 1 of the present invention;

[0033] FIG. 6(b) illustrates CO.sub.2 adsorption curves at 25° C. of 3MgO—TiO.sub.2 according to example 1 and example 2 of the present invention; and

[0034] FIG. 7 illustrates CO.sub.2 adsorption performance at 25° C. and 200° C. of 3MgO—TiO.sub.2 according to example 1 and example 2 of the present invention.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

[0035] Hereinafter, preferred embodiments of the present invention will be explained in detail.

[0036] The present invention relates to an adsorbent for capturing carbon dioxide comprising a magnesium oxide (MgO)/titanium dioxide (TiO.sub.2) composite.

[0037] Studies on a magnesium based metal oxide adsorbent for capturing CO.sub.2 are being conducted, but structural and morphological studies on an MgO/TiO.sub.2 composite for capturing CO.sub.2 have not been conducted until now. According to the present invention, the most efficient structure and morphology of an MgO/TiO.sub.2 composite for capturing CO.sub.2, and a method for manufacturing an adsorbent comprising the composite are provided.

[0038] The magnesium oxide/titanium dioxide composite according to the present invention is a composite in which MgO is incorporated into a TiO.sub.2 framework. Typically, the insertion of MgO into the TiO.sub.2 framework follows the formation of different phases including MgTiO.sub.3, MgTi.sub.2O.sub.4, Mg.sub.2TiO.sub.4 and MgTi.sub.2O.sub.5. Among them, the Mg.sub.2TiO.sub.4 phase has an inverse spinel structure of (B.sup.II).sup.tet(A.sup.IIB.sup.II).sup.octO.sub.4, and such a structure formed a relatively small amount of Mg—O—Ti base pairs and is somewhat shorts of CO.sub.2 capture performance when compared to other phases.

[0039] In the present invention, it was found that, by changing the composition ratio of Mg and Ti, an MgTi.sub.2O.sub.4 structure having a (A.sup.II).sup.tet(B.sup.III).sub.2.sup.octO.sub.4 structure which is a spinel structure similar to MgAl.sub.2O.sub.4 can be formed. In addition, Ti possess different oxidation states such as +2(Mg.sub.2TiO.sub.4), +3(MgTi.sub.2O.sub.4) and +4(MgTiO.sub.3), and in the present invention, it was confirmed that Ti having the oxidation state of +3 forms the strongest Mg—O—Ti ion pairs and serves favorable CO.sub.2 capture.

[0040] In particular, with respect to the insertion of MgO into the TiO.sub.2 framework, when the ratio of Mg/Ti is from 0.5 to 2.0, MgO—TiO.sub.2 forms an MgTiO.sub.3 structure. In addition, when the ratio of Mg/Ti is greater than 2.0 and less than 5.0, MgO—TiO.sub.2 forms an MgO—MgTi.sub.2O.sub.4 structure, and when the ratio of Mg/Ti is 5.0 or more, MgO—TiO.sub.2 forms an MgO—Mg.sub.2TiO.sub.4 structure.

[0041] In an example of the present invention, it was observed that when the ratio of Mg/Ti was greater than 2.0 and less than 5.0, that is, when forming an MgTi.sub.2O.sub.4 structure, CO.sub.2 adsorption performance was the best, and the surface area and the pore volume were the greatest. In particular, when the molar ratio of Mg/Ti was from 3.0 to 4.0, particularly good CO.sub.2 adsorption performance was attained.

[0042] The difference of CO.sub.2 adsorption performance depending on the Mg/Ti molar ratio may be explained as follows.

[0043] As verified in an XRD pattern analysis according to an example of the present invention, an MgO/TiO.sub.2 composite shows an MgTiO.sub.3 phase until the ratio of Mg/Ti reaches 2. The MgTiO.sub.3 crystalline phase has an ilmenite structure (ABO.sub.3) composed of AO6 (A=Mg) and BO6 (B=Ti) octahedron and forms weak Mg—O—Ti ion pairs.

[0044] Here, when the amount of Mg is increased and the ratio of Mg/Ti is greater than 2.0 and less than 5.0, the crystalline phases of MgO—TiO.sub.2, e.g., 3.0MgO—TiO.sub.2 and 4.0MgO—TiO.sub.2 change MgTiO.sub.3 to MgTi.sub.2O.sub.4. The MgTi.sub.2O.sub.4 crystalline phase with a structure of spindle AB.sub.2O.sub.4 contains element B in octahedral sites and A in tetrahedral sites. In addition, Ti has the oxidation state of Ti.sup.3+ which is the same as Al.sup.3+ in the MgAl.sub.2O.sub.4 spinel structure. This variation in the oxidation states of cationic sites could assist the generation of stronger Mg—O—Ti ion pairs and thus, induces better CO.sub.2 adsorption performance than the MgTiO.sub.3 crystalline phase.

[0045] However, with further increase in the addition of MgO, bulk MgO may be formed, and CO.sub.2 adsorption performance may be deteriorated, and in the case where the ratio of Mg/Ti is 5 or more, the phase changes to Mg.sub.2TiO.sub.4 crystalline phase. Since the Mg.sub.2TiO.sub.4 crystalline phase has an inverse spinel structure as described above, somewhat insufficient CO.sub.2 capture performance may be attained when compared to MgTi.sub.2O.sub.4 having a spinel structure.

[0046] Accordingly, in the present invention, by setting the molar ratio of Mg/Ti to greater than 2.0 and less than 5.0, a composite oxide adsorbent having an MgTi.sub.2O.sub.4 crystalline phase which is the most appropriate crystalline structure for the CO.sub.2 adsorption may be obtained.

[0047] Further, in an example of the present invention, it was confirmed through experiments that an adsorbent having the molar ratio of Mg/Ti of greater than 2.0 and less than 5.0 exhibited the best CO.sub.2 adsorption performance, and particularly, it was confirmed that an adsorbent having the molar ratio of Mg/Ti from 3.0 to 4.0 exhibited particularly good CO.sub.2 adsorption performance.

[0048] The adsorbent for capturing carbon dioxide comprising a magnesium oxide/titanium dioxide composite according to the present invention showed good CO.sub.2 adsorption performance at room temperature such as 25° C., and not inferior CO.sub.2 adsorption performance at a high temperature of 200° C. when compared to other well-known MgO based metal composites in literatures, and may be used for CO.sub.2 adsorption in various fields.

[0049] The magnesium oxide/titanium dioxide composite according to the present invention is formed by the self-assembly of a metal precursor including a magnesium precursor and a titanium precursor with a soft template which is a surfactant, and has a mesoporous structure.

[0050] In the present invention, the term “mesoporous” means a material containing pores having a diameter of mainly 2 to 50 nm.

[0051] In this aspect, the adsorbent for capturing carbon dioxide according to the present invention may be manufactured by dissolving a surfactant in a solvent; adding a metal precursor comprising a magnesium precursor and a titanium precursor and an acid in the solvent, and stirring; evaporating the solvent to obtain a self-assembled solid of the metal precursor and the surfactant; and calcining the solid at a temperature of 500° C. or more to remove the surfactant.

[0052] In the present invention, the solvent may be selected from ethanol, methanol, isopropyl alcohol and a combination thereof, and absolute ethanol is the most preferable.

[0053] In the present invention, the surfactant is preferably a soft template to obtain an ordered mesoporous composite metal oxide. The soft template may be a diblock or triblock copolymer, and the triblock copolymer is preferably used. The triblock copolymer used in the present invention may include polyethylene glycol-polypropylene glycol-polyethylene glycol (PEG-PPG-PEG), cetrimonium bromide, etc. More particularly, HO(CH.sub.2CH.sub.2O).sub.20(CH.sub.2CH(CH.sub.3)O).sub.70(CH.sub.2CH.sub.2O).sub.20H or HO(CH.sub.2CH.sub.2O).sub.100—(CH.sub.2(CH.sub.3)CHO).sub.65—(CH.sub.2CH.sub.2O).sub.100 may be used.

[0054] Hereinafter, the manufacturing process of the mesoporous composite metal oxide adsorbent of the present invention will be explained in detail referring to FIG. 1.

[0055] In the first step, a surfactant is dissolved in a solvent. When PEG-PPG-PEG triblock copolymer is used as a soft template surfactant, the surfactant may be dissolved in the solvent and present as a form of micelle. Then, a metal oxide and an acid are added thereto and stirred to form a cylindrical self-assembled micelle structure of PEG-PPG-PEG, and the metal oxide is positioned around the cylindrical micelles. After that, the solvent is evaporated to obtain a solid state in which the metal oxide is incorporated into the cylindrical PEG-PPG-PEG micelles. The solid is calcined at 500° C. or more to remove PEG-PPG-PEG, and a composite metal oxide adsorbent which maintains the shape of the template is formed. In this case, the composite metal oxide adsorbent has a cylindrically ordered mesoporous structure.

[0056] In the present invention, the magnesium precursor may comprise magnesium nitrate hexahydrate, magnesium acetate tetrahydrate, etc., and the magnesium nitrate hexahydrate is the most preferable.

[0057] In the present invention, the titanium precursor may comprise titanium isopropoxide or titanium tetrabutoxide, and the titanium isopropoxide is the most preferably used.

[0058] In the present invention, the self-assembly of a metal precursor and a soft template may preferably be conducted under acidic conditions, and an acid is preferably added together with the metal precursor. The acid may preferably be nitric acid, acetic acid, hydrochloric acid, sulfuric acid or a combination thereof, and the amount thereof may preferably be controlled to adjust pH to 4.0 to 6.0.

[0059] In the method of the present invention, the stirring may preferably be performed for a sufficient time period so that the metal precursor and the soft template may be sufficiently self-assembled. In an embodiment of the present invention, the stirring may preferably be performed for 4 to 10 hours.

[0060] In the present invention, the evaporation of the solvent may be performed using an appropriate well-known method depending on the kind of the solvent. For example, the evaporation of ethanol may preferably be performed at 50 to 70° C. for 24 to 72 hours. After completing the evaporation of the solvent, a self-assembled solid phase of the metal precursor and the soft template may be obtained.

[0061] The solid phase thus obtained may be calcined at 500° C. or higher to remove the surfactant, physico-chemically adsorbed water, impurities including volatile compounds, etc. The calcining is preferably performed for 4 to 10 hours to sufficiently remove the surfactant and the impurities. In an example of the present invention, it was confirmed that a magnesium oxide/titanium dioxide composite having high crystallinity without remaining impurities or residues may be obtained when performing calcination under the conditions of 500° C. or higher.

[0062] As described above, since the magnesium oxide/titanium dioxide composite formed by the self-assembly of a metal precursor and a soft template has a certain morphology, good CO.sub.2 capture performance may be exhibited when compared to a magnesium oxide/titanium dioxide composite having the same crystalline phase. However, an adsorbent for capturing carbon dioxide, having good stability and good CO.sub.2 adsorption performance may be provided even synthesizing a magnesium oxide/titanium dioxide composite not by the above-described method but by another method. Such embodiments are also included in the scope of the present invention. In addition, by setting the molar ratio of Mg/Ti of such magnesium oxide/titanium dioxide composite to 3 to 4, optimized CO.sub.2 adsorption performance may be attained. For example, in another embodiment of the present invention, MgO—TiO.sub.2 nanoparticles may be obtained using a precipitating agent such as NH.sub.4OH.

[0063] Hereinafter, the present invention will be described below in more detail with reference to particular embodiments. In the embodiments, experimental methods and components are partially explained to illustratively explain the present invention. However, the scope of the present invention is not limited to the embodiments.

Example 1: Synthesis of xMgO-TiO.SUB.2 .Adsorbent

[0064] 2.3 g of HO(CH.sub.2CH.sub.2O).sub.20(CH.sub.2CH(CH.sub.3)O).sub.70(CH.sub.2CH.sub.2O).sub.20H (Pluronic P.sub.123; Sigma Aldrich) was added as a triblock copolymer of a soft template to 50 ml of absolute ethanol (94.5%, Samchun Chemical Co.) and dissolved for 4 hours. Then, 5 g of titanium isopropoxide (Ti[OCH(CH.sub.3).sub.2]4, ≧97%, Sigma Aldrich) was dissolved therein, and 5 ml of nitric acid (70%) was added thereto. After stirring and a clear solution was obtained, magnesium nitrate hexahydrate (Mg(NO.sub.3).sub.2.6H.sub.2O) (99%, ACS reagent) was added so that the ratio of Mg/Ti became 0, 1, 2, 3, 4 and 5, respectively; followed by stirring for 5 hours. Then, the solution thus obtained was evaporated at 60° C. for 48 hours to induce the self-assembly of the metal precursor. The solid obtained after evaporating the solvent was calcined at 550° C. for 5 hours to obtain an ordered mesoporous adsorbent, xMgO-TiO.sub.2 (x=0, 1, 2, 3, 4 and 5).

Example 2: Synthesis of 3MgO—TiO.SUB.2 .Using NH.SUB.4.OH Precipitating Agent

[0065] A 3MgO—TiO.sub.2 composite metal oxide was synthesized using NH.sub.4OH as a precipitating agent. 5 g of titanium isopropoxide (≧97%, Sigma Aldrich) was added to 50 ml of an ethanol solution, and magnesium nitrate hexahydrate (99%, ACS reagent) was added so that the molar ratio of Mg/Ti was 3:1. Then, water was added to complete hydrolysis, and NH.sub.4OH was added as a precipitating agent. In this case, water and NH.sub.4OH were added so that the molar ratio of ethanol:water:NH.sub.4OH was 85:5:0.04. After that, the solution was stirred for 5 hours, and the solvent was evaporated at 60° C. for 48 hours. The solid thus obtained was calcined at 550° C. for 5 hours to finally obtain 3MgO—TiO.sub.2 nanoparticles as an adsorbent.

[0066] Analysis of Thermostability

[0067] 3MgO—TiO.sub.2 manufactured in each of example 1 and example 2 was heated in the atmosphere and thermogravimetric analysis (TGA) was performed. The results are shown in FIG. 2. As shown in FIG. 2, the thermal decomposition of both samples was completed at about 500° C. The TGA was performed at a heating rate of 5° C./min.

[0068] 3MgO—TiO.sub.2 synthesized in example 1 exhibited three major weight loss regions in different temperature ranges. The first region of weight loss, observed 25-150° C., typically assigned to the removal of the surface adsorbed species such as physically adsorbed water and volatile compounds. The second region which is the major weight loss, 150-250° C. is attributed to the decomposition of PEG units of surfactant P.sub.123. The third step was the weight loss in a range of 400-500° C., which was attributed to the dihydroxylation of M(Mg, Ti)-hydroxides and chemically adsorbed water, and to the complete conversion into perfect phases.

[0069] From such TGA, it was found that the magnesium oxide/titanium dioxide composite according to the present invention might completely form a composite structure at a relatively low temperature range of less than 550° C., and xMgO-TiO.sub.2 having high crystallinity might be grown by setting an appropriate calcination temperature.

[0070] In the case of the 3MgO—TiO.sub.2 nanoparticles synthesized in example 2, the mass loss took place stepwise assigned to water, structural hydroxyl groups and organic residues elimination, and the stabilization was also attained at about 500° C.

[0071] Analysis of Surface Characteristics

[0072] xMgO-TiO.sub.2 (x=0, 1, 2, 3, 4 and 5) synthesized in example 1 were analyzed by an N.sub.2 adsorption-desorption analysis at 298K using BELSORP-mini (BEL Japan Inc.), and the analysis results are shown in FIG. 3. FIG. 3(a) illustrates N.sub.2 adsorption-desorption isotherms, and FIG. 3(b) illustrates pore size distribution (PSD) curves.

[0073] In FIG. 3(a), all samples show a Type-IV adsorption isotherms and H1-type hysteresis loop, and from the results, it may be confirmed that the samples had a mesoporous structure.

[0074] The textural properties of the samples such as a specific surface area, a pore volume and a pore diameter were analyzed, and the results are shown in the table 1 below. The specific surface area was calculated by the BET method, the pore volume was obtained at a relative pressure (p/p.sub.0) of 0.99 in FIG. 3(a), and an average pore diameter was calculated from the adsorption branch of N.sub.2 isotherm by the BJH method. In addition, with respect to the samples synthesized in example 2, the specific surface area, the pore volume and the pore diameter were analyzed by the same method, and the results are shown together in table 1.

TABLE-US-00001 TABLE 1 Specific surface area Pore diameter Pore volume xMgO—TiO.sub.2 (m.sup.2/g) (nm) (cm.sup.3/g) 0MgO—TiO.sub.2 41.0 17.16 0.17 1MgO—TiO.sub.2 80.6 26.52 0.53 2MgO—TiO.sub.2 113.3 21.98 0.62 3MgO—TiO.sub.2 111.4 16.44 0.45 4MgO—TiO.sub.2 100.6 14.52 0.36 5MgO—TiO.sub.2 79.9 13.63 0.27 3MgO—TiO.sub.2 63.4 8.65 0.13 (NH.sub.4OH)

[0075] As confirmed in the above table 1, the specific surface area, the pore diameter and the pore volume increased with the increase of the molar ratio of Mg/Ti, but the specific surface area, the pore diameter and the pore volume decreased when the molar ratio of Mg/Ti was greater than 2. Among the adsorbents having the MgO—MgTi.sub.2O.sub.4 crystalline structure, 3MgO—TiO.sub.2 had the greatest specific surface area, pore diameter and pore volume.

[0076] In addition, 3MgO—TiO.sub.2 synthesized using NH.sub.4OH as a precipitating agent had the same composition ratio and crystalline phase as those of the 3MgO—TiO.sub.2 adsorbent having a mesoporous structure using a soft template, but had relatively small specific surface area, pore diameter and volume due to the structural difference.

[0077] Analysis of XRD Patterns

[0078] In order to analyze the XRD patterns of xMgO-TiO.sub.2 samples synthesize in example 1, XRD patterns were measured using XRD (D-Max2500-PC, Rigaku) with 20 value of 20 to 80. The measured results are shown in FIG. 4.

[0079] In FIG. 4, the pristine TiO.sub.2 in which Mg was not incorporated, possessed pure anatase phase as identified by ICDD file no. 01-078-2468. With further introduction of MgO in the TiO.sub.2 lattice has shown the phase transformation as shown in the table below.

TABLE-US-00002 TABLE 2 Mg/Ti ICDD file no. Phase 0 01-0787-2468 Anatase 1 01-079-0831 MgTiO.sub.3 2 01-079-0831 MgTiO.sub.3 3 01-074-2258 MgTi.sub.2O.sub.4 4 01-074-2258 MgTi.sub.2O.sub.4 5 01-079-0829 Mg.sub.2TiO.sub.4

[0080] As shown in the above table, the molar ratio of Mg/Ti was found to have a strong influence to the crystal structure of a composite. Specifically, with the increase of the molar ratio of Mg/Ti, the crystal phase was transformed as the following order: MgTiO.sub.3.fwdarw.MgO—MgTi.sub.2O.sub.4.fwdarw.MgO—Mg.sub.2TiO.sub.4.

[0081] Analysis of FE-TEM/FE-SEM Images

[0082] FE-SEM images of the 3MgO—TiO.sub.2 samples manufactured in example 1 were obtained by Helios 650 scanning electron microscope using an acceleration voltage of 15 kV. Prior to imaging the samples were sputter-coated with platinum coating. In addition, FE-TEM (Tecnai F20, FEI) analysis was carried out to examine the mesopore characteristics of the samples. Simultaneously, an energy dispersion spectroscopy (EDS)-elemental mapping was carried out in order to see the distribution of Mg, Ti and O throughout the composite and to assure the elemental compositions.

[0083] As confirmed from FIGS. 5(a) to 5(c), the TEM images of the samples showed the morphology of random stacking of spherical nanoparticles uniformly distributed with an average diameter of 10 nm or less dispersed throughout the sample. From FIG. 5(c), it was found that mesopores were evenly dispersed. In addition, the FE-SEM image of FIG. 5(d) showed the uniformly distributed particles stacked in irregular fashion. FIGS. 5(e) to 5(h) showed EDS-elemental mapping results, indicating the homogeneous distribution of the active metal species (Mg, Ti, O).

[0084] Analysis of CO.sub.2 Adsorption Performance

[0085] CO.sub.2 adsorption-desorption experiments were conducted using a thermogravimetric analyzer (SCINCO, TGA N-1000), which includes both physisorbed and chemisorbed CO.sub.2.

[0086] 20 mg of each adsorbent manufactured in example 1 and example 2 was placed in a platinum pan, and the adsorbent was pretreated at 200° C. for 30 min with a flow of N.sub.2 (60 ml/min). After cooling to the adsorption temperature (25° C.), the pure CO.sub.2 was introduced at a flow rate of 100 ml/min. Weight change due to the adsorption was then calculated in terms of mmol/g. The results thus obtained are shown in FIG. 6.

[0087] s confirmed in FIG. 6(a), the CO.sub.2 adsorption performance of the samples was increased with the increase of the molar ratio of Mg/Ti, and the best CO.sub.2 adsorption performance was attained at Mg/Ti=3. Then, the CO.sub.2 adsorption performance was decreased with the additional increase of the molar ratio of Mg/Ti. In addition, it may be confirmed that with respect to the 3MgO—TiO.sub.2 crystal having the same molar ratio of Mg/Ti of 3, an adsorbent manufactured using an NH.sub.4OH precipitating agent showed about half of the CO.sub.2 adsorption performance when compared to that of an adsorbent manufactured by the self-assembly of a soft template.

[0088] In order to confirm the influence according to the temperature, the CO.sub.2 adsorption performance was measured at 200° C. for 3MgO—TiO.sub.2 of example 1 and 3MgO—TiO.sub.2 of example 2, and the results were compared with those measured at 25° C. and are shown in FIG. 7. The measured results of the CO.sub.2 adsorption performance at 200° C. were confirmed to have about half of the CO.sub.2 adsorption performance measured at 25° C. for both samples of example 1 and example 2.

[0089] The results of FIGS. 6 and 7 are summarized and shown in table 3 below.

TABLE-US-00003 TABLE 3 CO.sub.2 adsorption CO.sub.2 adsorption performance performance xMgO—TiO.sub.2 (25° C., wt %) (200° C., wt %) 1MgO—TiO.sub.2 1.5 — 2MgO—TiO.sub.2 1.5 — 3MgO—TiO.sub.2 4.39 2.07 4MgO—TiO.sub.2 2.6 — 5MgO—TiO.sub.2 2.1 — 3MgO—TiO.sub.2 2.05 1.16 (NH.sub.4OH)

[0090] In particular, 3.0MgO—TiO.sub.2 according to example 1 showed the CO.sub.2 adsorption performance corresponding to 4.39 wt % (about 1 mmol/g), which was the best performance when compared to that of other adsorbents having different molar ratios of Mg/Ti. That is because strong Mg—O—Ti basic sites were formed due to the crystal structure in addition to the large surface area (111.4 m.sup.2/g) and pore volume (0.45 cm.sup.3/g) thereof. Even other adsorbents having different molar ratios showed lower CO.sub.2 adsorption performance when compared to that of 3MgO—TiO.sub.2, it was noted that the numerical values obtained therefrom also showed better than the CO.sub.2 adsorption performance of MgO based oxide adsorbents which have been reported in literature until now.

[0091] In addition, 3.0MgO—TiO.sub.2 according to example 1 showed better CO.sub.2 adsorption performance by twice than an adsorbent manufactured by using an NH.sub.4OH precipitating agent. That is because the adsorbent having a mesoporous structure formed by the self-assembly of a soft template and a metal precursor had a larger surface area, higher exposure of active site, and an ordered mesoporous structure than the adsorbent formed using an NH.sub.4OH precipitating agent.

[0092] Meanwhile, both adsorbents of example 1 and example 2 showed better CO.sub.2 adsorption performance when performing experiments at 25° C. than at 200° C., and the useful application of the adsorbents in the adsorption field at a low temperature CO.sub.2 was confirmed.

[0093] From the above-description, it can be understood that the present invention may be implemented in another preferred embodiments without changing the technical spirit or the essential configuration thereof by a person skilled in the art. In this regard, the above-disclosed exemplary embodiments are to be considered illustrative, and not restrictive. The scope of the present invention is to be interpreted to include all changes or modifications derived from the meaning and scope of the following claims and equivalents thereof rather than the foregoing detailed description.