METHOD FOR SEPARATING CO2 USING FACILITATED CO2 TRANSPORT MEMBRANE

Abstract

Provided is a facilitated CO.sub.2 transport membrane having an improved CO.sub.2 permeance and an improved CO.sub.2/H.sub.2 selectivity. The facilitated CO.sub.2 transport membrane includes a separation-functional membrane that includes a hydrophilic polymer gel membrane containing a CO.sub.2 carrier and a CO.sub.2 hydration catalyst. Further preferably, the CO.sub.2 hydration catalyst at least has catalytic activity at a temperature of 100? C. or higher, has a melting point of 200? C. or higher, or is soluble in water.

Claims

1. A method for separating CO.sub.2 using a facilitated CO.sub.2 transport membrane, the facilitated CO.sub.2 transport membrane comprising a separation-functional membrane that includes a hydrophilic polymer gel membrane containing a CO.sub.2 carrier with a CO.sub.2 hydration catalyst having catalytic activity at a temperature of 100? C. or higher, the method comprising: supplying a mixed gas containing CO.sub.2 and H.sub.2 and having a temperature of 100? C. or higher to a supply side of the facilitated CO.sub.2 transport membrane under a condition that a pressure difference between the supply side and a permeate side of the facilitated CO.sub.2 transport membrane is not less than 200 kPa, wherein the CO.sub.2 passing through the facilitated CO.sub.2 transport membrane is separated from the mixed gas, and wherein the CO.sub.2 hydration catalyst contains at least one of a tellurous acid compound, a selenious acid compound, an orthosilicic acid compound and a molybdic acid compound.

2. The method of claim 1, wherein the gel membrane is a hydrogel.

3. The method of claim 1, wherein the gel membrane is a polyvinyl alcohol-polyacrylic acid salt copolymer gel membrane.

4. The method of claim 1, wherein the CO.sub.2 carrier contains at least one of a carbonate of an alkali metal, a bicarbonate of an alkali metal and a hydroxide of an alkali metal.

5. The method of claim 4, wherein the alkali metal is cesium or rubidium.

6. The method of claim 1, wherein the separation-functional membrane is supported on a hydrophilic porous membrane.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0047] FIG. 1 is a sectional view schematically showing a structure in one embodiment of a facilitated CO.sub.2 transport membrane according to the present invention.

[0048] FIG. 2 is a flow chart showing a method for producing a facilitated CO.sub.2 transport membrane according to the present invention.

[0049] FIG. 3 is a table showing a list of constitutional conditions and membrane performance for separation-functional membranes of Examples 1 to 7 and Comparative Examples 1 and 2 used in experiments for evaluation of membrane performance of a facilitated CO.sub.2 transport membrane according to the present invention.

[0050] FIG. 4 is a graph showing a CO.sub.2 permeance and a CO.sub.2/H.sub.2 selectivity in Examples 1 to 5 and Comparative Example 1 shown in FIG. 3.

[0051] FIG. 5 is a graph showing a CO.sub.2 permeance and a CO.sub.2/H.sub.2 selectivity in Examples 1 and 6 and Comparative Examples 1 and 2 shown in FIG. 3.

[0052] FIG. 6 is a graph showing a CO.sub.2 permeance and a CO.sub.2/H.sub.2 selectivity in Examples 1 and 7 and Comparative Example 1 shown in FIG. 3.

[0053] FIG. 7 is a table showing a list of constitutional conditions and membrane performance for separation-functional membranes of Examples 2, and 8 to 10 and Comparative Examples 1, 4 and 5 used in experiments for evaluation of membrane performance of a facilitated CO.sub.2 transport membrane according to the present invention.

[0054] FIG. 8 is a graph showing a CO.sub.2 permeance and a CO.sub.2/H.sub.2 selectivity in Examples 2 and 8 and Comparative Examples 1 and 4 shown in FIG. 7.

[0055] FIGS. 9A and 9B are configuration diagrams each schematically showing an outlined configuration in one embodiment of a CO.sub.2 separation apparatus according to the present invention.

DESCRIPTION OF EMBODIMENTS

[0056] By extensively conducting studies, the inventors of the present application have found that when a gel membrane of a facilitated CO.sub.2 transport membrane, which contains a CO.sub.2 carrier and in which a reaction of CO.sub.2 with the CO.sub.2 carrier as expressed by the above (Chemical Formula 2) occurs, contains a catalyst for a CO.sub.2 hydration reaction as expressed by the above (Chemical Formula 1), one of elementary reactions of the above-mentioned reaction, the catalyst being capable of maintaining catalytic activity without being deactivated at a high temperature of 100? C. or higher, the CO.sub.2 permeance is dramatically improved with respect to the H.sub.2 permeance even at such a high temperature, and the CO.sub.2/H.sub.2 selectivity is considerably improved as compared to a conventional facilitated CO.sub.2 transport membrane that does not contain the catalyst. Based on the above-mentioned new finding, the inventors of the present application have completed the invention of a facilitated CO.sub.2 transport membrane and a method for producing the same, and a method and an apparatus for separating CO.sub.2 as shown below.

First Embodiment

[0057] First, one embodiment of a facilitated CO.sub.2 transport membrane and a method for producing the same according to the present invention (hereinafter, referred to as the present facilitated transport membrane and the present production method as appropriate) will be described with reference to the drawings.

[0058] The present facilitated transport membrane is a facilitated CO.sub.2 transport membrane including a separation-functional membrane that includes a water-containing hydrophilic polymer gel membrane containing a CO.sub.2 carrier and a CO.sub.2 hydration catalyst having catalytic activity at a temperature of 100? C. or higher, the facilitated CO.sub.2 transport membrane serving at a temperature of 100? C. or higher and having a high CO.sub.2 permeance and a high CO.sub.2/H.sub.2 selectivity, and the facilitated CO.sub.2 transport membrane being applicable to a CO.sub.2 permeable membrane reactor or the like. Further, for stably achieving a high CO.sub.2/H.sub.2 selectivity, the present facilitated transport membrane includes a hydrophilic porous membrane as a support membrane that supports a gel membrane containing a CO.sub.2 carrier and a CO.sub.2 hydration catalyst.

[0059] Specifically, the present facilitated transport membrane includes a polyvinyl alcohol-polyacrylic acid (PVA/PAA) salt copolymer as a membrane material of the separation-functional membrane, a carbonate of an alkali metal such as cesium carbonate (Cs.sub.2CO.sub.3) or rubidium carbonate (Rb.sub.2CO.sub.3) as the CO.sub.2 carrier, and an oxo acid compound as the CO.sub.2 hydration catalyst. More specifically, for the CO.sub.2 hydration catalyst, an oxo acid compound of at least one element selected from group 6 elements, group 14 elements, group 15 elements and group 16 elements is used, and particularly preferably a tellurous acid compound, a selenious acid compound, an arsenious acid compound, an orthosilicic acid compound or a molybdic acid compound is used. All of CO.sub.2 hydration catalysts used in this embodiment are soluble in water, and extremely thermally stable with a melting point of 400? C. or higher, and have catalytic activity at a high temperature of 100? C. or higher. The melting point of the CO.sub.2 hydration catalyst is only required to be higher than the upper limit of temperature variations in steps in a method for producing the present facilitated transport membrane as described later (e.g. the temperature in the drying step or thermal crosslinking temperature). When the melting point is, for example, about 200? C. or higher, a situation is avoided in which the CO.sub.2 hydration catalyst is sublimed in the course of the production process, leading to a reduction in concentration of the CO.sub.2 hydration catalyst in the separation-functional membrane.

[0060] As an example, the present facilitated transport membrane is configured as a three-layer structure in which a hydrophilic porous membrane 2 supporting a separation-functional membrane 1 is held between two hydrophobic porous membranes 3 and 4 as schematically shown in FIG. 1. The separation-functional membrane 1 as a gel membrane is supported on the hydrophilic porous membrane 2 and has a certain level of mechanical strength, and therefore is not necessarily required to be held between the two hydrophobic porous membranes 3 and 4. The mechanical strength can also be increased by, for example, forming the hydrophilic porous membrane 2 in a cylindrical shape. Therefore, the present facilitated transport membrane is not necessarily a flat plate-shaped one.

[0061] The separation-functional membrane contains the PVA/PAA salt copolymer in an amount falling within a range of about 10 to 80% by weight, and the CO.sub.2 carrier in an amount falling within a range of about 20 to 90% by weight based on the total weight of the PVA/PAA salt copolymer and the CO.sub.2 carrier in the separation-functional membrane.

[0062] Further, the separation-functional membrane contains the CO.sub.2 hydration catalyst, for example, in an amount of 0.01 times or more, preferably 0.02 times or more, further preferably 0.025 times or more the amount of the CO.sub.2 carrier in terms of molar number.

[0063] The hydrophilic porous membrane preferably has heat resistance to a temperature of 100? C. or higher, mechanical strength and adhesion with the separation-functional membrane (gel membrane) in addition to hydrophilicity, and preferably has a porosity (void ratio) of 55% or more and a pore size falling within a range of 0.1 to 1 ?m. In this embodiment, a hydrophilized tetrafluoroethylene polymer (PTFE) porous membrane is used as a hydrophilic porous membrane that satisfies the above-mentioned requirements.

[0064] The hydrophobic porous membrane preferably has heat resistance to a temperature of 100? C. or higher, mechanical strength and adhesion with the separation-functional membrane (gel membrane) in addition to hydrophobicity, and preferably has a porosity (void ratio) of 55% or more and a pore size falling within a range of 0.1 to 1 ?m. In this embodiment, a non-hydrophilized tetrafluoroethylene polymer (PTFE) porous membrane is used as a hydrophobic porous membrane that satisfies the above-mentioned requirements.

[0065] One embodiment of a method for producing the present facilitated transport membrane (the present production method) will now be described with reference to FIG. 2. The following descriptions are based on the assumption that a PVA/PAA salt copolymer is used as the hydrophilic polymer, cesium carbonate (Cs.sub.2CO.sub.3) is used as the CO.sub.2 carrier, and a tellurite (e.g. potassium tellurite (K.sub.2TeO.sub.3)) is used as the CO.sub.2 hydration catalyst. The amounts of the hydrophilic polymer, the CO.sub.2 carrier and the CO.sub.2 hydration catalyst are illustrative, and show amounts used in sample preparation in examples described below.

[0066] First, a cast solution including an aqueous solution containing a PVA/PAA salt copolymer, a CO.sub.2 carrier and a CO.sub.2 hydration catalyst is prepared (step 1). More specifically, 2 g of a PVA/PAA salt copolymer (e.g. provisional name: SS Gel manufactured by Sumitomo Seika Chemicals Company Limited), 4.67 g of cesium carbonate, and a tellurite in an amount of 0.025 times the amount of cesium carbonate in terms of molar number are added to 80 g of water, and the resultant mixture is stirred until they are dissolved, thereby obtaining a cast solution.

[0067] Next, the cast solution obtained in step 1 is cast on a hydrophilic PTFE porous membrane side surface of a layered porous membrane by an applicator (step 2), the layered porous membrane being obtained by joining two membranes: a hydrophilic PTFE porous membrane (e.g. WPW-020-80 manufactured by SUMITOMO ELECTRIC FINE POLYMER, INC.; thickness: 80 ?m; pore size: 0.2 ?m; void ratio: about 75%) and a hydrophobic PTFE porous membrane (e.g. FLUOROPORE FP010 manufactured by SUMITOMO ELECTRIC FINE POLYMER, INC.; thickness: 60 ?m; pore size: 0.1 ?m; void ratio: 55%). The casting thickness in samples of examples and comparative examples described later is 500 ?m. Here, the cast solution penetrates pores in the hydrophilic PTFE porous membrane, but is inhibited from penetrating at the boundary surface of the hydrophobic PTFE porous membrane, so that the cast solution does not permeate to the opposite surface of the layered porous membrane, and there is no cast solution on a hydrophobic PTFE porous membrane side surface of the layered porous membrane. This makes handling easy.

[0068] Next, the hydrophilic PTFE porous membrane after casting is naturally dried at room temperature, and the cast solution is then gelled to produce a separation-functional membrane (step 3). Here, gelation means that the cast solution as a polymer dispersion liquid is dried into a solid form, and the gel membrane is a solid membrane produced by the gelation, and is clearly distinguished from a liquid membrane.

[0069] In the present production method, the cast solution is cast on a hydrophilic PTFE porous membrane side surface of the layered porous membrane in step 2, and therefore the separation-functional membrane is not only formed on a surface (cast surface) of the hydrophilic PTFE porous membrane but also formed so as to fill pores in step 3, so that defects (minute defects such as pinholes) are hard to occur, leading to an increase in membrane production success rate of the separation-functional membrane. It is desirable to further thermally crosslink the naturally dried PTFE porous membrane at about 120? C. for about 2 hours in step 3. All of samples in examples and comparative examples described later are thermally crosslinked.

[0070] Next, a hydrophobic PTFE porous membrane identical to the hydrophobic PTFE porous membrane of the layered porous membrane used in step 2 is superimposed on a gel layer side surface of the hydrophilic PTFE porous membrane obtained in step 3 to obtain the present facilitated transport membrane of three layer structure including a hydrophobic PTFE porous membrane/a separation-functional membrane supported on a hydrophilic PTFE porous membrane/a hydrophobic PTFE porous membrane as schematically shown in FIG. 1 (step 4). FIG. 1 schematically and linearly shows a state in which the separation-functional membrane 1 fills pores of the hydrophilic PTFE porous membrane 2.

[0071] In the present production method, the blending ratio of the CO.sub.2 carrier and the CO.sub.2 hydration catalyst can be adjusted in step 1 of producing a cast solution, and therefore, as compared to a case where after formation of a gel membrane that does not contain at least one of the CO.sub.2 carrier and the CO.sub.2 hydration catalyst, at least one of the CO.sub.2 carrier and the CO.sub.2 hydration catalyst is added into the gel membrane, adjustment of the blending ratio can be more accurately and easily performed, leading to enhancement of membrane performance.

[0072] Thus, the present facilitated transport membrane prepared by following steps 1 to 4 can exhibit extremely high selective permeability to hydrogen even at a high temperature of 100? C. or higher, for example a CO.sub.2 permeance of about 3?10.sup.?5 mol/(m.sup.2.Math.s.Math.kPa) (=90 GPU) or more and a CO.sub.2/H.sub.2 selectivity of about 100 or more.

[0073] Hereinafter, specific membrane performance of the present facilitated transport membrane is evaluated by comparing Examples 1 to 7 in which the separation-functional membrane contains a CO.sub.2 hydration catalyst with Comparative Examples 1 and 2 in which the separation-functional membrane does not contain a CO.sub.2 hydration catalyst.

[0074] The samples in Examples 1 to 7 and Comparative Examples 1 and 2 below were prepared in accordance with the present production method described above. The weights of the solvent (water), the hydrophilic polymer and the CO.sub.2 carrier in the cast solution prepared in step 1 are the same among Examples 1 to 7 and Comparative Examples 1 and 2. As the hydrophilic polymer, a PVA/PAA salt copolymer was used. As the CO.sub.2 carrier, cesium carbonate (Cs.sub.2CO.sub.3) is used except for Example 6, and the weight ratio of cesium carbonate to the total weight of the PVA/PAA salt copolymer and cesium carbonate (carrier concentration) is 70% by weight in each of the examples and comparative examples. In Example 6, rubidium carbonate (Rb.sub.2CO.sub.3) is used as the CO.sub.2 carrier, and the weight ratio of rubidium carbonate to the total weight of the PVA/PAA salt copolymer (2 g) identical to that in Example 1 and rubidium carbonate (4.67 g) (carrier concentration) is 70% by weight.

[0075] In Examples 1, 6 and 7, potassium tellurite (melting point: 465? C.) was used as the CO.sub.2 hydration catalyst. In Examples 2 to 5, lithium tellurite (Li.sub.2O.sub.3Te, melting point: about 750? C.), potassium selenite (K.sub.2O.sub.3Se, melting point: 875? C.), sodium arsenite (NaO.sub.2As, melting point: 615? C.) and sodium orthosilicate (Na.sub.4O.sub.4Si, melting point: 1018? C.) were used, respectively, as the CO.sub.2 hydration catalyst. The molar ratio of the CO.sub.2 hydration catalyst to the CO.sub.2 carrier is 0.025 in Examples 1 to 5, 0.05 in Example 6, and 0.2 in Example 7.

[0076] The sample in Comparative Example 1 was prepared in the same manner as in Example 1 except that the cast solution prepared in step 1 in the production method described above did not contain a CO.sub.2 hydration catalyst. The sample in Comparative Example 2 was prepared in the same manner as in Example 6 except that the cast solution prepared in step 1 in the production method described above did not contain a CO.sub.2 hydration catalyst.

[0077] An experiment method for evaluating membrane performance of the samples in Examples 1 to 7 and Comparative Examples 1 and 2 will now be described.

[0078] Each sample was used while being fixed between a supply side chamber and a permeate side chamber in a stainless steel flow type gas permeation cell using a fluororubber gasket as a seal material. Experimental conditions are the same for the samples, and the temperature of the inside of the cell is fixed at 130? C.

[0079] The supply side gas supplied to the supply side chamber is a mixed gas including CO.sub.2, H.sub.2 and H.sub.2O (steam), and the ratio (mol %) among them is CO.sub.2:H.sub.2:H.sub.2O=23.6:35.4:41.0. The flow rate of the supply side gas is 3.47?10.sup.?2 mol/min, and the supply side pressure is 600 kPa (A). (A) means an absolute pressure. Accordingly, the CO.sub.2 partial pressure on the supply side is 142 kPa (A). The pressure of the supply side chamber is adjusted with a back pressure regulator provided on the downstream side of a cooling trap at some midpoint in an exhaust gas discharging passage.

[0080] On the other hand, the pressure of the permeate side chamber is atmospheric pressure, H.sub.2O (steam) is used as a sweep gas made to flow into the permeate side chamber, and the flow rate thereof is 7.77?10.sup.?3 mol/min. For sending the sweep gas discharged from the permeate side chamber to a gas chromatograph on the downstream side, an Ar gas is inpoured, steam in the gas containing the Ar gas is removed by the cooling trap, the composition of the gas after passing through the cooling trap is quantitatively determined by the gas chromatograph, the permeance [mol/(m.sup.2.Math.s.Math.kPa)] of each of CO.sub.2 and H.sub.2 is calculated from the composition and the flow rate of Ar in the gas, and from the ratio thereof, the CO.sub.2/H.sub.2 selectivity is calculated.

[0081] In the evaluation experiment described above, the experiment apparatus has a pre-heater for heating the gas and the flow type gas permeation cell with a sample membrane fixed therein is placed in a thermostatic oven in order to keep constant the use temperature of the present facilitated transport membrane of each sample and the temperatures of the supply side gas and the sweep gas.

[0082] Next, comparison of membrane performance obtained in experiment results in Examples 1 to 7 and Comparative Examples 1 and 2 is made. FIG. 3 shows a list of constitutional conditions (CO.sub.2 carrier, CO.sub.2 hydration catalyst, molar ratio of CO.sub.2 carrier to CO.sub.2 hydration catalyst, hydrophilic polymer) and membrane performance (CO.sub.2 permeance, H.sub.2 permeance and CO.sub.2/H.sub.2 selectivity) for separation-functional membranes of the samples in Examples 1 to 7 and Comparative Examples 1 and 2.

[0083] First, comparison of membrane performance is made among Examples 1 to 5 and Comparative Example 1. Here, comparison of membrane performance associated with presence/absence of the CO.sub.2 hydration catalyst and the type thereof is made. FIG. 4 shows, in the form of a graph, the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity in Examples 1 to 5 and Comparative Example 1. It is apparent from FIGS. 3 and 4 that since the separation-functional membrane contains a CO.sub.2 hydration catalyst, the CO.sub.2 permeance increases by a factor of 1.14 to 1.76, while the H.sub.2 permeance increases by a factor of 0.72 to 1.29, and the increasing rate of CO.sub.2 permeance is greater than that of H.sub.2 permeance, so that the CO.sub.2/H.sub.2 selectivity is improved to fall within a range of 104 to 135 as compared to a CO.sub.2/H.sub.2 selectivity of 79.2 in Comparative Example 1.

[0084] While from FIG. 4, all of the CO.sub.2 hydration catalysts are confirmed to improve both the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity, the CO.sub.2 permeance is remarkably improved when a tellurite is used.

[0085] Since the CO.sub.2 hydration catalyst is a catalyst for increasing the reaction rate of a CO.sub.2 hydration reaction expressed by the above (Chemical Formula 1), it is considered that when the separation-functional membrane contains a CO.sub.2 hydration catalyst, a reaction of CO.sub.2 with a CO.sub.2 carrier, which includes the CO.sub.2 hydration reaction as one of elementary reactions and which is expressed by the above (Chemical Formula 2), is accelerated, leading to an increase in CO.sub.2 permeance by the facilitated transport mechanism. This is consistent with the experiment results shown in FIG. 3. However, since H.sub.2 does not react with the CO.sub.2 carrier as described above, the H.sub.2 permeation mechanism may be based on the solution-diffusion mechanism rather than the facilitated transport mechanism, and it is considered that the H.sub.2 permeance is not directly affected by presence/absence of the CO.sub.2 hydration catalyst, the blending ratio and type thereof, and the like. Further, the samples in Examples 1 to 7 and Comparative Examples 1 and 2 are different in constitutional conditions for the separation-functional membrane, and are therefore each individually prepared. Therefore, differences in measurement value of H.sub.2 permeance among the samples are considered to mainly result from individual differences (variations) in membrane quality of the hydrophilic polymer gel membrane. It is to be noted that the H.sub.2 permeance may be indirectly affected by influences on membrane quality of the hydrophilic polymer gel membrane given by differences in amount, type and the like of the CO.sub.2 carrier and the CO.sub.2 hydration catalyst in addition to the individual differences in membrane quality.

[0086] Next, comparison of membrane performance is made among Examples 1 and 6 and Comparative Examples 1 and 2. Here, comparison of membrane performance associated with presence/absence of the CO.sub.2 hydration catalyst and the type the CO.sub.2 carrier is made. FIG. 5 shows, in the form of a graph, the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity in Examples 1 and 6 and Comparative Examples 1 and 2. FIG. 5 shows that when the separation-functional membrane does not contain a CO.sub.2 hydration catalyst, there is no significant difference in performance due to a difference in CO.sub.2 carrier with the separation-functional membrane having a CO.sub.2 permeance of 2.83 to 2.84?10.sup.?5 (mol/(m.sup.2.Math.s.Math.kPa)), a H.sub.2 permeance of 3.05 to 3.58?10.sup.?7 (mol/(m.sup.2.Math.s.Math.kPa)) and a CO.sub.2/H.sub.2 selectivity of 79.2 to 93.1 in both cases where the CO.sub.2 carrier is cesium carbonate and where the CO.sub.2 carrier is rubidium carbonate. When the CO.sub.2 carrier is cesium carbonate, performance is greatly improved with the CO.sub.2 permeance increasing by a factor of 1.53, the H.sub.2 permeance increasing by a factor of 1.02 and the CO.sub.2/H.sub.2 selectivity increasing by a factor of 1.50 because the separation-functional membrane contains a CO.sub.2 hydration catalyst. When the CO.sub.2 carrier is rubidium carbonate, performance is greatly improved as in the case where the CO.sub.2 carrier is cesium carbonate, with the CO.sub.2 permeance increasing by a factor of 1.68, the H.sub.2 permeance increasing by a factor of 0.83 and the CO.sub.2/H.sub.2 selectivity increasing by a factor of 2.04. The reason why in Example 6, the H.sub.2 permeance decreases to 0.83 times that in Comparative Example 2 may be because of individual differences in membrane quality of the hydrophilic polymer gel membrane.

[0087] Next, comparison of membrane performance is made among Examples 1 and 7 and Comparative Example 1. Here, comparison of membrane performance associated with presence/absence of the CO.sub.2 hydration catalyst, and the blending ratio thereof (molar ratio to cesium carbonate) is made. FIG. 6 shows, in the form of a graph, the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity in Examples 1 and 7 and Comparative Example 1.

[0088] When comparison is made among Comparative Example 1 and Examples 1 and 7, it is apparent that both the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity are improved as the blending ratio of the CO.sub.2 hydration catalyst (potassium tellurite) increases.

[0089] As a result of measuring the CO.sub.2 permeance with another sample in which the molar ratio of the CO.sub.2 hydration catalyst to the CO.sub.2 carrier is decreased to 0.01 when the hydrophilic polymer is a PVA/PAA salt copolymer, the CO.sub.2 carrier is cesium carbonate and the CO.sub.2 hydration catalyst is potassium tellurite, aside from Examples 1 and 7, it has been confirmed that the CO.sub.2 permeance was improved to 3.74?10.sup.?5 (mol/(m.sup.2.Math.s.Math.kPa)), i.e. 1.32 times the CO.sub.2 permeance in Comparative Example 1.

[0090] While all of the separation-functional membranes in Examples 1 to 7 and Comparative Examples 1 and 2 are gel membranes, Comparative Example 3 having a liquid membrane (aqueous solution) as a separation-functional membrane was prepared as another comparative example. The aqueous solution of a separation-functional membrane in Comparative Example 3 does not contain the PVA/PAA salt copolymer used in Examples 1 to 7 and Comparative Example 1. In Comparative Example 3, cesium carbonate was used as a CO.sub.2 carrier and potassium tellurite was used as a CO.sub.2 hydration catalyst similarly to Example 1. Hereinafter, a method for preparing Comparative Example 3 will be described.

[0091] To an aqueous cesium carbonate solution having a molar concentration of 2 mol/L was added potassium tellurite in an amount of 0.025 times the amount of cesium carbonate in terms of molar number, and the resultant mixture was stirred until potassium tellurite was dissolved, thereby obtaining an aqueous solution for a separation-functional membrane (liquid membrane). Thereafter, instead of the casting method using an applicator in step 2 in the present production method, a hydrophilic PTFE porous membrane was immersed in the aqueous solution for a separation-functional membrane (liquid membrane) for 30 minutes, and the hydrophilic PTFE membrane soaked with the aqueous solution was then placed on a hydrophobic PTFE membrane, and dried at room temperature for half a day or longer. Similarly to Examples 1 to 7 and Comparative Examples 1 and 2, another hydrophobic PTFE membrane is placed on the hydrophilic PTFE membrane to form a three-layer structure with the hydrophilic PTFE porous membrane and the separation-functional membrane (liquid membrane) held between the hydrophobic PTFE membranes at the time of an experiment for evaluation of membrane performance.

[0092] However, in the case of the liquid membrane sample of Comparative Example 3, it was impossible to set the supply side pressure of 600 kPa (A), i.e. an experimental condition similar to that in Examples 1 to 7 and Comparative Examples 1 and 2, and membrane performance could not be evaluated. That is, it became evident that a necessary differential pressure cannot be maintained because the difference in pressure between the supply side and the permeate side in the separation-functional membrane (liquid membrane) cannot be endured.

[0093] Thus, by comparing membrane performance between Examples 1 to 7 in which the separation-functional membrane contains a CO.sub.2 hydration catalyst and Comparative Examples 1 and 2 in which the separation-functional membrane does not contain a CO.sub.2 hydration catalyst, an effect of considerably improving the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity was confirmed as the present facilitated transport membrane includes a CO.sub.2 hydration catalyst in the separation-functional membrane. Here, the facilitated CO.sub.2 transport membrane has such characteristics that in a certain thickness range, thickness dependency is kept low, so that the permeation rate of CO.sub.2 hardly decreases even when the thickness increases. On the other hand, H.sub.2 passes through the separation-functional membrane by the solution-diffusion mechanism as described above, and therefore its permeation rate tends to be inversely proportional to the membrane thickness. Therefore, further improvement of the CO.sub.2/H.sub.2 selectivity is expected due to the synergistic effect of the advantage that the effect of improving the CO.sub.2 permeance due to presence of a CO.sub.2 hydration catalyst in the separation-functional membrane is attained without depending on the membrane thickness and the advantage that the H.sub.2 permeance is reduced as the thickness is increased.

[0094] Results of evaluating membrane performance in Examples 8 and 9 in which the separation-functional membrane prepared with a thickness that is about 2 times the thickness in Examples 1 to 7 and Comparative Examples 1 and 2 contains a CO.sub.2 hydration catalyst and Comparative Example 4 in which the separation-functional membrane does not contain a CO.sub.2 hydration catalyst will now be described.

[0095] The samples in Examples 8 and 9 and Comparative Example 4 were prepared in accordance with the present production method described above. It is to be noted that a series of steps including step 2 and step 3 were repeated twice for increasing the thickness of the separation-functional membrane. The weights of the solvent (water), the hydrophilic polymer and the CO.sub.2 carrier in the cast solution prepared in step 1 are the same among Examples 8 and 9 and Comparative Example 4, and identical to those in Examples 1 to 7 and Comparative Examples 1 and 2. In each of Examples 8 and 9 and Comparative Example 4, cesium carbonate (Cs.sub.2CO.sub.3) is used as the CO.sub.2 carrier, and the weight ratio of cesium carbonate to the total weight of the PVA/PAA salt copolymer and cesium carbonate (carrier concentration) is 70% by weight.

[0096] In Examples 8 and 9, lithium tellurite and potassium molybdate (K.sub.2O.sub.4Mo, melting point: about 919? C.) were used in this order as the CO.sub.2 hydration catalyst. The molar ratio of the CO.sub.2 hydration catalyst to the CO.sub.2 carrier is 0.025 in Example 8, and 0.1 in Example 9. The sample in Comparative Example 4 was prepared in the same manner as in Example 8 except that the cast solution prepared in step 1 in the production method described above did not contain a CO.sub.2 hydration catalyst.

[0097] An experiment method for evaluating membrane performance of the samples in Examples 8 and 9 and Comparative Example 4 is identical to the experiment method for evaluating membrane performance of the samples in Examples 1 to 7 and Comparative Examples 1 and 2 described above including the gas composition and ratio of the supply side gas, the gas flow rate, the pressure, the use temperature and so on.

[0098] FIG. 7 shows a list of constitutional conditions (CO.sub.2 carrier, CO.sub.2 hydration catalyst, molar ratio of CO.sub.2 carrier to CO.sub.2 hydration catalyst, hydrophilic polymer) and membrane performance (CO.sub.2 permeance, H.sub.2 permeance and CO.sub.2/H.sub.2 selectivity) for separation-functional membranes of the samples in Examples 2, 8 and 9 and Comparative Examples 1 and 4. FIG. 8 shows, in the form of a graph, the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity in Examples 2 and 8 and Comparative Examples 1 and 4.

[0099] First, when comparison of membrane performance is made between Comparative Example 4 and Comparative Example 1, the membrane thickness in Comparative Example 4 is about 2 times the membrane thickness in Comparative Example 1, but there is no difference in other constitutional conditions of the separation-functional membrane, and therefore there is substantially no difference in CO.sub.2 permeance as it is not significantly influenced by the membrane thickness, whereas the H.sub.2 permeance is much lower in Comparative Example 4 than in Comparative Example 1 due to the about 2-fold difference in membrane thickness. As a result, the CO.sub.2/H.sub.2 selectivity is higher in Comparative Example 4 than in Comparative Example 1. Similarly, when comparison of membrane performance is made between Example 8 and Example 2, the membrane thickness in Example 8 is about 2 times the membrane thickness in Example 2, but there is no difference in other constitutional conditions of the separation-functional membrane, and therefore there is substantially no difference in CO.sub.2 permeance as it is not significantly influenced by the membrane thickness, and an effect of improving the CO.sub.2 permeance by the CO.sub.2 hydration catalyst is similarly attained, whereas the H.sub.2 permeance is much lower in Example 8 than in Example 2 due to the about 2-fold difference in membrane thickness. As a result, the CO.sub.2/H.sub.2 selectivity is higher in Example 8 than in Example 2. When comparison of membrane performance is made between Example 8 and Comparative Example 4, it is apparent that similarly to considerable improvement of the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity in Example 2 as compared to Comparative Example 1, the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity are considerably improved even when the thickness of the separation-functional membrane is large. That is, it has become evident that the effect of improving the CO.sub.2 permeance due to presence of a CO.sub.2 hydration catalyst in the separation-functional membrane is attained without depending on the thickness of the separation-functional membrane in a certain thickness range.

[0100] Next, when comparison is made between Example 9 and Comparative Example 4, an effect of improving the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity due to presence of a CO.sub.2 hydration catalyst in the separation-functional membrane can be confirmed even with a membrane thickness that is about 2 times the membrane thickness in Examples 1 to 7 also when the CO.sub.2 hydration catalyst is potassium molybdate.

[0101] Here, the CO.sub.2 hydration catalyst in each of Examples 1 to 3 and 6 to 8 and Example 10 described later is an oxo acid compound of a group 16 element, the CO.sub.2 hydration catalyst in Example 4 is an oxo acid compound of a group 15 element, the CO.sub.2 hydration catalyst in Example 5 is an oxo acid compound of a group 14 element, and the CO.sub.2 hydration catalyst in Example 9 is an oxo acid compound of a group 6 element. Accordingly, from the results of evaluating membrane performance, it is apparent that at least oxo acid compounds of group 6 elements, group 14 elements, group 15 elements and group 16 elements suitably include a CO.sub.2 hydration catalyst which is soluble in water and extremely thermally stable with a melting point of 200? C. or higher, and has catalytic activity at a high temperature of 100? C. or higher. However, this does not mean that all the oxo acid compounds of group 6 elements, group 14 elements, group 15 elements and group 16 elements have catalytic activity as a CO.sub.2 hydration catalyst, and the possibility is not ruled out that oxo acid compounds other than those of group 6 elements, group 14 elements, group 15 elements and group 16 elements include those which have catalytic activity as a CO.sub.2 hydration catalyst and can be used for the present facilitated transport membrane.

[0102] Further, as substances having catalytic activity as a CO.sub.2 hydration catalyst, there are many substances other than oxo acid compounds, such as enzymes. Therefore, the CO.sub.2 hydration catalyst is not limited to the oxo acid compounds used in Examples 1 to 9 as long as it can be suitably used for the present facilitated transport membrane. Here, as an example of conditions suitable for the present facilitated transport membrane as a CO.sub.2 hydration catalyst, the substance is soluble in water, and extremely thermally stable with a melting point of 200? C. or higher, and has catalytic activity at a high temperature of 100? C. or higher.

[0103] In the above-mentioned embodiment, as an example of a suitable configuration of the present facilitated transport membrane, a configuration has been shown in which a hydrogel of a PVA/PAA salt copolymer as a hydrophilic polymer is used as a membrane material of a separation-functional membrane, and a hydrophilic porous membrane is used as a porous membrane that supports the separation-functional membrane. However, since the hydrophilic polymer gel membrane contains a CO.sub.2 hydration catalyst, the effect of improving the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity can also be exhibited, although varying in level, when a hydrophilic polymer other than PVA/PAA salt copolymers, such as, for example, polyvinyl alcohol (PVA) or a polyacrylic acid (PAA) salt is used, or when a hydrophobic porous membrane is used as a porous membrane that supports the separation-functional membrane.

[0104] Results of evaluating membrane performance in Example 10 in which the separation-functional membrane contains a CO.sub.2 hydration catalyst and Comparative Example 5 in which the separation-functional membrane does not contain a CO.sub.2 hydration catalyst, with polyvinyl alcohol (PVA) being used as a hydrophilic polymer in both Example 10 and Comparative Example 5, will now be described.

[0105] The samples in Example 10 and Comparative Example 5 were prepared in accordance with the present production method described above. It is to be noted that similarly to Examples 8 and 9 and Comparative Example 4, a series of steps including step 2 and step 3 were repeated twice for increasing the thickness of the separation-functional membrane. The weights of the solvent (water), the hydrophilic polymer and the CO.sub.2 carrier in the cast solution prepared in step 1 are the same between Example 10 and Comparative Example 5. In each of Example 10 and Comparative Example 5, cesium carbonate (Cs.sub.2CO.sub.3) is used as the CO.sub.2 carrier, and the weight ratio of cesium carbonate to the total weight of PVA and cesium carbonate (carrier concentration) is 46% by weight. The polymerization degree of polyvinyl alcohol used is about 2000, and the porous membrane supporting the separation-functional membrane is a PTFE porous membrane having a pore size of 0.1 ?m and a thickness of 50 ?m.

[0106] In Example 10, potassium tellurite is used as a CO.sub.2 hydration catalyst, and the molar ratio of the CO.sub.2 hydration catalyst to the CO.sub.2 carrier is 0.2. The sample in Comparative Example 5 was prepared in the same manner as in Example 10 except that the cast solution prepared in step 1 in the production method described above did not contain a CO.sub.2 hydration catalyst.

[0107] An experiment method for evaluating membrane performance of the samples in Example 10 and Comparative Example 5 is identical to the experiment method for evaluating membrane performance of the samples in Examples 1 to 9 and Comparative Examples 1, 2 and 4 described above except for the ratio of gas components of the supply side gas, the supply side gas flow rate, the supply side pressure and the use temperature. The ratio (mol %) among CO.sub.2, H.sub.2 and H.sub.2O (steam) in the supply side gas supplied to the supply side chamber is CO.sub.2:H.sub.2:H.sub.2O=5.0:48.7:46.3. The flow rate of the supply side gas is 6.14?10.sup.?2 mol/min, the supply side pressure is 300 kPa (A), and the temperature of the inside of the flow type gas permeation cell is fixed at 120? C.

[0108] FIG. 7 shows a list of constitutional conditions (CO.sub.2 carrier, CO.sub.2 hydration catalyst, molar ratio of CO.sub.2 carrier to CO.sub.2 hydration catalyst, hydrophilic polymer) and membrane performance (CO.sub.2 permeance, H.sub.2 permeance and CO.sub.2/H.sub.2 selectivity) for separation-functional membranes of the samples in Example 10 and Comparative Example 5.

[0109] When comparison of membrane performance is made between Example 10 and Comparative Example 5, it is apparent that the CO.sub.2 permeance and CO.sub.2/H.sub.2 selectivity are considerably improved. From this result, it has become evident that the effect of improving the CO.sub.2 permeance due to presence of a CO.sub.2 hydration catalyst in the separation-functional membrane is attained also when polyvinyl alcohol is used as the hydrophilic polymer. Accordingly, it is well conceivable that the effect of improving the CO.sub.2 permeance is attained irrespective of the composition of the hydrophilic polymer. Therefore, the hydrophilic polymer that forms the separation-functional membrane of the present facilitated transport membrane is not limited to the PVA/PAA salt copolymer and polyvinyl alcohol (PVA) shown as examples in the above-mentioned embodiment.

Second Embodiment

[0110] A CO.sub.2 separation apparatus and a CO.sub.2 separation method, to which the facilitated CO.sub.2 transport membrane described in the first embodiment is applied, will now be described with reference to FIGS. 9A and 9B.

[0111] FIGS. 9A and 9B are each a sectional view schematically showing an outlined structure of a CO.sub.2 separation apparatus 10 of this embodiment. In this embodiment, as an example, a facilitated CO.sub.2 transport membrane modified into a cylindrical structure is used instead of the facilitated CO.sub.2 transport membrane of flat plate structure described in the first embodiment. FIG. 9A shows a cross section structure at a cross section perpendicular to the axial center of a facilitated CO.sub.2 transport membrane (the present facilitated transport membrane) 11 of cylindrical structure, and FIG. 9B shows a cross section structure at a cross section extending through the axial center of the present facilitated transport membrane 11.

[0112] The present facilitated transport membrane 11 shown in FIGS. 9A and 9B has a structure in which a separation-functional membrane 1 is supported on the outer circumferential surface of a cylindrical hydrophilic ceramic porous membrane 2. Similarly to the first embodiment, the separation-functional membrane 1 includes a polyvinyl alcohol-polyacrylic acid (PVA/PAA) salt copolymer as a membrane material of the separation-functional membrane, a carbonate of an alkali metal such as cesium carbonate (Cs.sub.2CO.sub.3) or rubidium carbonate (Rb.sub.2CO.sub.3) as the CO.sub.2 carrier, and a tellurous acid compound, a selenious acid compound, an arsenious acid compound and an orthosilicic acid compound as the CO.sub.2 hydration catalyst. The membrane structure in this embodiment is different from the membrane structure in the first embodiment in that the separation-functional membrane 1 and the hydrophilic ceramic porous membrane 2 are not held between two hydrophobic porous membranes. The method for producing the separation-functional membrane 1 and membrane performance thereof in this embodiment are basically similar to those in the first embodiment except for the above-mentioned difference, and therefore duplicate explanations are omitted.

[0113] As shown in FIGS. 9A and 9B, the present cylindrical facilitated transport membrane 11 is housed in a bottomed cylindrical container 12, and a supply side space 13 surrounded by the inner wall of the container 12 and the separation-functional membrane 1 and a permeate side space 14 surrounded by the inner wall of the ceramic porous membrane 2 are formed. A first feeding port 15 for feeding a source gas FG into the supply side space 13 and a second feeding port 16 for feeding a sweep gas SG into the permeate side space 14 are provided on one of bottom portions 12a and 12b on opposite sides of the container 12, and a first discharge port 17 for discharging a CO.sub.2-separated source gas EG from the supply side space 13 and a second discharge port 18 for discharging from the permeate side space 14 a discharge gas SG including a mixture of a CO.sub.2-containing permeate gas PG passing through the present facilitated transport membrane 11 and the sweep gas SG are provided on the other of the bottom portions 12a and 12b on opposite sides of the container 12. The container 12 is made of, for example, stainless steel, and although not illustrated, the present facilitated transport membrane 11 is fixed in the container 12 with a fluororubber gasket interposed as a seal material between opposite ends of the present facilitated transport membrane 11 and the inner walls of the bottom portions 12a and 12b on opposite sides of the container 12 similarly to the experiment apparatus described in the first embodiment as an example. The method for fixing the present facilitated transport membrane 11 and the sealing method are not limited to the methods described above.

[0114] In FIG. 9B, each of the first feeding port 15 and the first discharge port 17 is provided in each of the supply side spaces 13 illustrated separately on the left and the right in FIG. 9B. However, since the supply side spaces 13 annularly communicate with each other as shown in FIG. 9A, the first feeding port 15 and the first discharge port 17 may be provided in one of the left and right supply side spaces 13. Further, FIG. 9B shows as an example a configuration in which the first feeding port 15 and the second feeding port 16 are provided on one of the bottom portions 12a and 12b, and the first discharge port 17 and the second discharge port 18 are provided on the other of the bottom portions 12a and 12b, but a configuration may be employed in which the first feeding port 15 and the second discharge port 18 are provided on one of the bottom portions 12a and 12b, and the first discharge port 17 and the second feeding port 16 are provided on the other of the bottom portions 12a and 12b. That is, the direction along which the source gases FG and EG flow and the direction along which the sweep gas SG and the discharge gas SG flow may be reversed.

[0115] In the CO.sub.2 separation method of this embodiment, the source gas FG including a mixed gas containing CO.sub.2 and H.sub.2 and having a temperature of 100? C. or higher is fed into the supply side space 13 and thereby supplied to the supply side surface of the present facilitated transport membrane 11, so that a CO.sub.2 carrier contained in the separation-functional membrane 1 of the present facilitated transport membrane 11 is reacted with CO.sub.2 in the source gas FG to allow selective passage of CO.sub.2 at a high selection ratio to hydrogen, and the CO.sub.2-separated source gas EG having an increased H.sub.2 concentration is discharged from the supply side space 13.

[0116] The reaction of CO.sub.2 with the CO.sub.2 carrier requires supply of water (H.sub.2O) as shown in the above reaction formula of (Chemical Formula 2), and as the amount of water contained in the separation-functional membrane 1 increases, chemical equilibrium is shifted to the product side (right side), so that permeation of CO.sub.2 is facilitated. When the temperature of the source gas FG is a high temperature of 100? C. or higher, the separation-functional membrane 1 that is in contact with the source gas FG is also exposed to a high temperature of 100? C. or higher, so that water contained in the separation-functional membrane 1 is evaporated and passes into the permeate side space 14 similarly to CO.sub.2, and therefore it is necessary to supply steam (H.sub.2O) to the supply side space 13. The steam may be contained in the source gas FG, or may be supplied to the supply side space 13 independently of the source gas FG. In the latter case, steam (H.sub.2O) passing into the permeate side space 14 may be separated from the discharge gas SG and circulated into the supply side space 13.

[0117] For the CO.sub.2 separation apparatus shown in FIGS. 9A and 9B, a configuration example has been described in which the supply side space 13 is formed at the outside while the permeate side space 14 is formed at the inside of the present cylindrical facilitated transport membrane 11, but the supply side space 13 may be formed at the inside while the permeate side space 14 may be formed at the outside. The present facilitated transport membrane 11 may have a structure in which the separation-functional membrane 1 is supported on the inner circumferential surface of the cylindrical hydrophilic ceramic porous membrane 2. Further, the present facilitated transport membrane 11 used in the CO.sub.2 separation apparatus is not necessarily cylindrical, but may be in the form of a tube having a cross-sectional shape other than a circular shape, and the present facilitated transport membrane of flat plate structure as shown in FIG. 1 may be used.

[0118] As an application example of the CO.sub.2 separation apparatus described in this embodiment, a shift converter (CO.sub.2 permeable membrane reactor) including the present facilitated transport membrane will now be briefly described.

[0119] For example, when a CO.sub.2 permeable membrane reactor is formed using the CO.sub.2 separation apparatus 10 shown in FIGS. 9A and 9B, the supply side space 13 can be used as a shift converter by filling the supply side space 13 with a shift catalyst.

[0120] The CO.sub.2 permeable membrane reactor is an apparatus in which, for example, a source gas FG produced in a steam reforming device and having H.sub.2 as a main component is received in the supply side space 13 filled with a shift catalyst, and carbon monoxide (CO) contained in the source gas FG is removed through a CO shift reaction expressed by the above (Chemical Formula 5). CO.sub.2 produced through the CO shift reaction is allowed to permeate to the permeate side space 14 selectively by means of the present facilitated transport membrane 11 and removed, whereby chemical equilibrium can be shifted to the hydrogen production side, so that CO and CO.sub.2 can be removed beyond the limit imposed by equilibrium restriction with a high conversion rate at the same reaction temperature. A source gas EG freed of CO and CO.sub.2 and having H.sub.2 as a main component is taken out from the supply side space 13.

[0121] Since the performance of the shift catalyst used for the CO shift reaction tends to decrease with a decrease in temperature, the use temperature is considered to be 100? C. at minimum, and the temperature of the source gas FG supplied to the supply side surface of the present facilitated transport membrane 11 is 100? C. or higher. Therefore, the source gas FG is adjusted to a temperature suitable for catalytic activity of the shift catalyst, then fed into the supply side space 13 filled with the shift catalyst, subjected to the CO shift reaction (exothermic reaction) in the supply side space 13, and supplied to the present facilitated transport membrane 11.

[0122] On the other hand, the sweep gas SG is used for maintaining the driving force for the permeation through the present facilitated transport membrane 11 by lowering the partial pressure of the CO.sub.2-containing permeate gas PG which permeates the present facilitated transport membrane 11 and for discharging the permeate gas PG to the outside. It is to be noted that when the partial pressure of the source gas FG is sufficiently high, it is not necessary to feed the sweep gas SG because a partial pressure difference serving as the driving force for permeation is obtained even if the sweep gas SG is not fed. As a gas species used for the sweep gas, steam (H.sub.2O) can also be used as in the case of the experiment for evaluation of membrane performance in the first embodiment, and further an inert gas such as Ar can also be used. The sweep gas SG is not limited to a specific gas species.

[0123] [Other Embodiments]

[0124] Hereinafter, other embodiments will be described.

[0125] <1> The above-mentioned embodiments have been described based on the assumption that a carbonate, a bicarbonate or a hydroxide of an alkali metal such as cesium or rubidium is used as a CO.sub.2 carrier. However, since the present invention is characterized in that a hydrophilic polymer gel membrane that forms a separation-functional membrane contains a CO.sub.2 carrier and a CO.sub.2 hydration catalyst having catalytic activity at a high temperature of 100? C. or higher, the CO.sub.2 carrier is not limited to a specific CO.sub.2 carrier as long as it is such a CO.sub.2 carrier that a reaction of CO.sub.2 with the CO.sub.2 carrier can be accelerated by a CO.sub.2 hydration catalyst to attain membrane performance comparable to or higher than the membrane performance (selective permeability of CO.sub.2 to hydrogen) shown as an example in the first embodiment.

[0126] <2> The above-mentioned embodiments have been described based on the assumption that the CO.sub.2 hydration catalyst contains at least one of a tellurous acid compound, a selenious acid compound, an arsenious acid compound, an orthosilicic acid compound and a molybdic acid compound, but the CO.sub.2 hydration catalyst is not limited to a specific CO.sub.2 hydration catalyst as long as it is a CO.sub.2 hydration catalyst which has catalytic activity for the CO.sub.2 hydration reaction of the above (Chemical Formula 1) at a high temperature of 100? C. or higher, preferably 130? C. or higher, more preferably 160? C. or higher and which can attain membrane performance comparable to or higher than the membrane performance (selective permeability of CO.sub.2 to hydrogen) shown as an example in the first embodiment when combined with a CO.sub.2 carrier. When used in the separation-functional membrane of the present facilitated transport membrane, the CO.sub.2 hydration catalyst is preferably one that has a melting point of 200? C. or higher and is soluble in water similarly to the above-mentioned compounds. While the upper limit of the range of temperatures at which the CO.sub.2 hydration catalyst exhibits catalytic activity is not particularly limited, there is no problem as long as it is higher than the upper limit of the range of temperatures such as the use temperature of the present facilitated transport membrane in an apparatus including the present facilitated transport membrane, and the temperature of a source gas supplied to the supply side surface of the present facilitated transport membrane. The hydrophilic porous membrane or the like that forms the present facilitated transport membrane is also required to have resistance in a similar temperature range as a matter of course. When the present facilitated transport membrane is used at a temperature lower than 100? C., the CO.sub.2 hydration catalyst is not necessarily required to have catalytic activity at a high temperature of 100? C. or higher.

[0127] <3> In the first embodiment, the present facilitated transport membrane is prepared by a method in which a cast solution including an aqueous solution containing a hydrophilic polymer (PVA/PAA salt copolymer, polyvinyl alcohol (PVA) or the like), a CO.sub.2 carrier and a CO.sub.2 hydration catalyst is cast on a hydrophilic PTFE porous membrane, and then gelled, but the present facilitated transport membrane may be prepared by a preparation method other than the above-mentioned preparation method. For example, the present facilitated transport membrane may be prepared by forming a hydrophilic polymer gel membrane that does not contain a CO.sub.2 carrier and a CO.sub.2 hydration catalyst, followed by impregnating the gel membrane with an aqueous solution containing a CO.sub.2 carrier and a CO.sub.2 hydration catalyst.

[0128] <4> In the first embodiment, the present facilitated transport membrane has a three-layer structure including a hydrophobic PTFE porous membrane, a separation-functional membrane supported on a hydrophilic PTFE porous membrane and a hydrophobic PTFE porous membrane, but the support structure of the present facilitated transport membrane is not limited to such a three-layer structure. For example, the present facilitated transport membrane may have a two-layer structure including a hydrophobic PTFE porous membrane and a separation-functional membrane supported on a hydrophilic PTFE porous membrane. In the first embodiment, a case has been described where the separation-functional membrane is supported on the hydrophilic PTFE porous membrane, but the separation-functional membrane may be supported on the hydrophobic PTFE porous membrane.

[0129] <5> In the second embodiment, a CO.sub.2 permeable membrane reactor has been described as an application example of the CO.sub.2 separation apparatus including the present facilitated transport membrane, but the CO.sub.2 separation apparatus including the present facilitated transport membrane can also be used in a decarbonation step in a hydrogen production process other than that in the membrane reactor, and is further applicable to processes other than the hydrogen production process, and the CO.sub.2 separation apparatus is not limited to the application example shown in the above-mentioned embodiment. The supply side gas (source gas) supplied to the present facilitated transport membrane is not limited to the mixed gas shown as an example in the above-mentioned embodiments.

[0130] <6> The mixing ratios of the components in the composition of the present facilitated transport membrane, the dimensions of the portions of the membrane and the like as shown as examples in the above-mentioned embodiments are examples given for easy understanding of the present invention, and the present invention is not limited to facilitated CO.sub.2 transport membranes having such values.

INDUSTRIAL APPLICABILITY

[0131] A facilitated CO.sub.2 transport membrane according to the present invention can be used for separating CO.sub.2 from a mixed gas including CO.sub.2 and H.sub.2 at a high selection ratio to hydrogen in a decarbonation step in a hydrogen production process, a CO.sub.2 permeable membrane reactor, and so on, and is useful particularly for separation of CO.sub.2 at a high temperature of 100? C. or higher.

DESCRIPTION OF SYMBOLS

[0132] 1 separation-functional membrane

[0133] 2 hydrophilic porous membrane

[0134] 3, 4 hydrophobic porous membrane

[0135] 10 CO.sub.2 separation apparatus

[0136] 11 facilitated CO.sub.2 transport membrane

[0137] 12 container

[0138] 12a, 12b bottom portion (upper bottom portion and lower bottom portion) of container

[0139] 13 supply side space

[0140] 14 permeate side space

[0141] 15 first feeding port

[0142] 16 second feeding port

[0143] 17 first discharge port

[0144] 18 second discharge port

[0145] FG source gas

[0146] EG CO.sub.2-separated source gas

[0147] PG permeate gas

[0148] SG, SG sweep gas