The present invention relates to a method for separating carbon dioxide. More specifically, the present invention relates to a method for separating carbon dioxide, which is performed by a membrane separation using an inorganic separation membrane.
As to the carbon dioxide (CO2) contained in a natural gas that includes methane (CH4) as the main component, for example, in a case where a natural gas is transported by using a pipeline, from the viewpoint of improving the heating value per unit gas volume, preventing the pipeline corrosion, and the like, it is required to recover and remove carbon dioxide from a natural gas. Conventionally, as a recovery method of carbon dioxide, a technique such as a chemical absorption method utilizing an amine absorbent or the like, or a physical adsorption method such as a pressure swing adsorption method (PSA) is used, but the energy consumption accompanying regeneration of an absorbent or an adsorbent is large, and therefore, development of a more highly efficient recovery method has been expected.
On the other hand, a process of carbon dioxide separation from a natural gas using a membrane separation has been known as a technique by which the energy can be saved as compared with a carbon dioxide separation process using an existing absorbent or the like. Further, a separation membrane made of a polymer (hereinafter, also referred to as a “polymer membrane”), which has been used as a separation membrane, has a low separation performance, and has a problem in the chemical resistance and the like, therefore, in recent years, a membrane separation using an inorganic separation membrane, which is capable of performing a continuous operation, has a high separation performance, and is excellent in the chemical resistance, has been performed(for example, see JP 2012-236134 A).
In separating carbon dioxide by a membrane separation using an inorganic separation membrane, in order to efficiently enable permeable components to permeate, a driving force that is a partial pressure difference of carbon dioxide between on the carbon dioxide non-permeation side and on the carbon dioxide permeation side in an inorganic separation membrane is required to be maintained. On the other hand, when a membrane having a high separation performance such as an inorganic separation membrane is used, partial pressure of the carbon dioxide on the carbon dioxide permeation side is increased, and the partial pressure difference between on the carbon dioxide non-permeation side and on the permeation side is decreased when the mixed gas that is a raw material is separated up to in the vicinity of the desired concentration, therefore, the driving force is hardly obtained, and thus there has been a problem that the membrane area to be required is increased. Further, because the polymer membrane used so far has a low separation performance, it is not required to consider the maintenance of the driving force, and the like in the application range of a polymer membrane, and the problem is generated only in a case of the separation by applying an inorganic separation membrane, therefore, the specific investigation has not been made so far, and it is urgently required to take measures for this problem. In addition, as to the membrane separation, there is problem that the cost is high and the like when the membrane area of the inorganic separation membrane is large, therefore, it was has been required to suppress the membrane area as small as possible.
The present invention has been made to solve the problems as described above, and to provide a method for separating carbon dioxide in which in separating carbon dioxide from a mixed gas containing methane and the carbon dioxide by a membrane separation using an inorganic separation membrane, the membrane area of the inorganic separation membrane can be suppressed smaller while maintaining the driving force that is a partial pressure difference of carbon dioxide between on the carbon dioxide non-permeation side and on the carbon dioxide permeation side.
According to the present invention, in order to solve the above problems, there is provided a method for separating carbon dioxide, including: separating carbon dioxide from a mixed gas containing methane and the carbon dioxide by a membrane separation, wherein in a case where a carbon dioxide mole fraction at a final outlet on a carbon dioxide non-permeation side is expressed as XCO2, a carbon dioxide mole fraction on a carbon dioxide permeation side corresponding to the final outlet on the carbon dioxide non-permeation side is expressed as YCO2, carbon dioxide non-permeation side pressure is expressed as PX, and carbon dioxide permeation side pressure is expressed as PY, in a separation membrane system provided with an inorganic separation membrane that is permeated by the carbon dioxide preferentially from the mixed gas, the carbon dioxide is membrane-separated from the mixed gas such that a carbon dioxide partial pressure difference ΔP expressed by the following Formula (I) at the final outlet on the carbon dioxide non-permeation side is ⅕ or more of a carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2).
Mathematical Formula 1
ΔP=PXXCO2−PYYCO2 (I)
According to the method for separating carbon dioxide of the present invention, the carbon dioxide is membrane-separated such that the carbon dioxide partial pressure difference ΔP is ⅗ or less of the carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2).
According to the method for separating carbon dioxide of the present invention, an ideal separation factor α of the inorganic separation membrane being provided to the separation membrane system is expressed by the following Formula (II).
According to the method for separating carbon dioxide of the present invention, an ideal separation factor α of the inorganic separation membrane being provided to the separation membrane system is expressed by the following Formula (III).
According to the method for separating carbon dioxide of the present invention, the method is used when carbon dioxide is separated from the mixed gas such that a carbon dioxide mole fraction at the final outlet on the carbon dioxide non-permeation side XCO2 is a ratio (PY/PX) or less of the carbon dioxide permeation side pressure PY to the carbon dioxide non-permeation side pressure PX.
According to the method for separating carbon dioxide of the present invention, carbon dioxide is separated from the mixed gas in the range of PX from 2.1 to 6.1 [MPaA], in the range of PY from 0.10 to 0.25 [MPaA], and in the range of XCO2 from 0.01 to 0.03.
According to the present invention, a method for separating carbon dioxide is as follows. In a separation membrane system provided with an inorganic separation membrane that is permeated by carbon dioxide preferentially from a mixed gas containing methane and the carbon dioxide, the carbon dioxide is membrane-separated from the mixed gas such that a carbon dioxide partial pressure difference ΔP at the final outlet on the carbon dioxide non-permeation side is ⅕ or more of the carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2), therefore, the driving force that is a partial pressure difference of carbon dioxide between on the carbon dioxide non-permeation side and on the carbon dioxide permeation side is maintained, and further the membrane area of the inorganic separation membrane to be used can be suppressed smaller, the carbon dioxide can be efficiently separated, and the cost is low.
Hereinafter, as to one example of the embodiments of the present invention, a method for separating carbon dioxide according to the present invention will be described by using a separation membrane system 1 shown in
The mixed gas to be a raw material, which is subjected to the separation in the present invention, is a mixed gas containing carbon dioxide (CO2) and methane (CH4). The inorganic separation membrane 2 used in the separation membrane system 1 is permeated by carbon dioxide preferentially from the above-described mixed gas, and the mixed gas is supplied from an input part 3 to an inorganic separation membrane 2l. The inorganic separation membrane 2l is permeated by carbon dioxide selectively from the mixed gas to be supplied, the carbon dioxide (permeable component) is taken out, and the remaining components (non-permeable components) containing methane as the main component are separated and sent to an inorganic separation membrane 2m. In the same manner, the inorganic separation membrane 2m arranged on the non-permeation side of the inorganic separation membrane 2l is permeated by carbon dioxide selectively from the non-permeable components of the inorganic separation membrane 2l to be supplied, the carbon dioxide (permeable component) is taken out, and the remaining components (non-permeable components) containing methane as the main component are separated and sent to an inorganic separation membrane 2n. For the following inorganic separation membrane 2n, the same operation is performed, and thus carbon dioxide is separated from the mixed gas. Further, the term “non-permeation side” and “permeation side” used in
In addition, in
Herein, as described above, the mixed gas, which is a raw material, is a mixed gas containing carbon dioxide (CO2) and methane (CH4). Examples of the raw material source of the mixed gas include a natural gas, and a biogas obtained from organic wastes (biomass) or the like, and the present invention can be used as a measure for separating carbon dioxide and taking out methane from the mixed gas.
In the separation membrane system 1 shown in
As the kind of the inorganic separation membrane 2, it is not particularly limited, and a conventionally known inorganic separation membrane 2 such as a zeolite membrane, a silica membrane, or a carbon membrane, can be used. Among them, as the zeolite membrane, for example, a zeolite membrane such as a CHA (chabazite) type, a SAPO (silicoaluminophosphate) type, a DDR (Deca-Dodecasil 3R) type, a MFI type, or a FAU (faujasite) type can be used.
The configuration (shape, module structure, and the like) of the inorganic separation membrane 2 is not particularly limited, and is appropriately determined by the desired concentration, or the like. Further, the inorganic separation membrane 2 may be used in a form of a multitubular, that is, a so-called separation membrane module, for example, a separation membrane module with a shell & tube type structure in a heat exchanger can be used.
In the present invention, the ideal separation factor α indicates a ratio (α=K—CO2/K—CH4) of the permeance of carbon dioxide (K—CO2) (mol/(m2·Pa·s)) and the permeance of methane (K—CH4) (mol/(m2·Pa·s)) under the performance conditions for an inorganic separation membrane 2. Accordingly, it is indicated that as to the inorganic separation membrane 2, as the ideal separation factor α is larger (the permeance of carbon dioxide per unit permeance of methane is larger), the permeation performance of carbon dioxide is better.
Herein, the carbon dioxide partial pressure difference ΔP is indicated by the difference between the carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2) and the carbon dioxide partial pressure on the carbon dioxide permeation side (PY·YCO2) in the separation membrane system 1. In Formula (I), ΔP indicates the carbon dioxide partial pressure difference [MPa] at the final outlet on the carbon dioxide non-permeation side, PX indicates the carbon dioxide non-permeation side pressure [MPaA] (substantially common to the pressure on the mixed gas supply side (raw material side), the same applies hereinafter), XCO2 indicates the carbon dioxide mole fraction [−] at the final outlet on the carbon dioxide non-permeation side ((hereinafter also simply referred to as the “carbon dioxide mole fraction [−] on the carbon dioxide non-permeation side”), PY indicates the carbon dioxide permeation side pressure [MPaA], and YCO2 indicates the carbon dioxide mole fraction [−] on the carbon dioxide permeation side corresponding to the final outlet on the carbon dioxide non-permeation side ((hereinafter also simply referred to as “carbon dioxide mole fraction [−] on the carbon dioxide permeation side”). Herein, “the carbon dioxide permeation side corresponding to the final outlet on the carbon dioxide non-permeation side” indicates “the carbon dioxide permeation side which is positioned while sandwiching the inorganic separation membrane 2 to the final outlet on the carbon dioxide non-permeation side, and on which the carbon dioxide mole fraction on the carbon dioxide permeation side YCO2 can be specified”.
[Mathematical Formula 4]
ΔP=PXXCO2−PYYCO2 (I)
In Formula (I), under the condition that the carbon dioxide partial pressure difference ΔP is extremely small, ΔP≈0, which is approximately equal, therefore, Formula (I) is expressed by Formula (A1).
[Mathematical Formula 5]
P
X
X
CO2
−P
Y
Y
CO2≈0 (A1)
From the Formula (A1), the carbon dioxide partial pressure difference ΔP becomes extremely small, and ΔP≈0, which is approximately equal, therefore, the carbon dioxide mole fraction on the carbon dioxide non-permeation side XCO2 can be expressed by Formula (A2).
[Mathematical Formula 6]
X
CO2
≈P
Y
Y
CO2
/P
X (A2)
In a case where an ideal separation factor α indicating a membrane performance of the inorganic separation membrane 2 (permeance ratio of carbon dioxide and methane) is extremely large, the permeation amount of methane is extremely small, and the carbon dioxide mole fraction on the carbon dioxide permeation side is substantially 1.0 (YCO2≈1.0), therefore, the carbon dioxide mole fraction on the carbon dioxide non-permeation side XCO2 becomes the following Formula (A3).
[Mathematical Formula 7]
X
CO2
≈P
Y
/P
X (A3)
From the above, it is considered that in a case where the carbon dioxide partial pressure in the mixed gas to be supplied is lowered until the condition that the mole fraction of carbon dioxide at the final outlet on the carbon dioxide non-permeation side XCO2 is a ratio (PY/PX ) or less of the carbon dioxide permeation side pressure PY to the carbon dioxide non-permeation side pressure PX is obtained, by the value of the ideal separation factor of the inorganic separation membrane 2, a condition in which the carbon dioxide partial pressure difference that is driving force of a membrane separation is extremely decreased is generated.
Next,
As shown in
Further, the carbon dioxide permeation side pressure (dashed line) (hereinafter also simply referred to as “permeation side pressure”) in the inorganic separation membrane 2 becomes substantially constant. It is considered that the carbon dioxide permeation side pressure shows almost the same behavior even for an inorganic separation membrane having any value of ideal separation factor irrespective of the ideal separation factor of the inorganic separation membrane 2.
In the separation membrane system 1, a pressure difference is generated between on the carbon dioxide non-permeation side and on the carbon dioxide permeation side of the inorganic separation membrane 2, and by using the pressure difference as the driving force, the carbon dioxide preferentially permeates the inorganic separation membrane 2. In order to efficiently enable permeable components to permeate, it is required that the driving force that is a carbon dioxide partial pressure difference between on the carbon dioxide non-permeation side and on the carbon dioxide permeation side is maintained high (the carbon dioxide partial pressure on the carbon dioxide non-permeation side is higher than that on the carbon dioxide permeation side).
As shown in
Further, as shown in
In the present invention, at first, as shown in
Further, at the intersection point of the line indicating the carbon dioxide partial pressure on the carbon dioxide non-permeation side with the carbon dioxide permeation side pressure, the carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2) and the carbon dioxide permeation side pressure (PY) become equal to each other (PY=PX·XCO2), therefore, “XCO2=PY/PX” is satisfied.
The carbon dioxide partial pressure difference ΔP at the outlet on the carbon dioxide non-permeation side of the separation membrane system 1 is determined by the carbon dioxide partial pressure difference between on the carbon dioxide non-permeation side and on the carbon dioxide permeation side, which is shown in the above-described Formula (I). In the separation method according to the present invention, the membrane separation is performed by the separation membrane system 1 provided with an inorganic separation membrane 2 that is permeated by carbon dioxide preferentially from a mixed gas, such that the carbon dioxide partial pressure difference ΔP expressed by Formula (I) at the final outlet on the carbon dioxide non-permeation side is ⅕ or more of the carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2). When the relationship is expressed by equation, the following Formula (II-1) is obtained.
As to the relationship among the carbon dioxide partial pressure difference ΔP, the membrane area of an inorganic separation membrane 2, and methane (CH4) recovery rate indicated in
In addition, the carbon dioxide non-permeation side pressure PX, the carbon dioxide permeation side pressure PY, and the carbon dioxide mole fraction at the final outlet on the carbon dioxide non-permeation side (carbon dioxide mole fraction on the carbon dioxide non-permeation side) XCO2 are used as predetermined conditions, and the carbon dioxide separation from a mixed gas such that the carbon dioxide mole fraction in a mixed gas (supply gas carbon dioxide mole fraction) X0 becomes an intended mole fraction (XCO2) is calculated (simulated) by using various ideal separation factors α (permeance ratio of carbon dioxide and methane), and further the methane (CH4) recovery rate is calculated from the methane (CH4) permeation amount (or the methane (CH4) amount on the carbon dioxide non-permeation side) in each case. From the above, it is summarized as the relationship to ΔP. Further, it is summarized as the relationship to ΔP by calculating the membrane area required in each case. In the drawing, points (rhombus: ⋄) plotted on the solid line indicating the membrane area and points (triangle: Δ) plotted on the dashed-dotted line indicating the methane recovery rate are points corresponding to individual ideal separation factors α, and as the carbon dioxide partial pressure difference ΔP is smaller, the value corresponding to the larger ideal separation factor α is shown, respectively. Herein, as to ΔP, from the calculation (simulation) results, the value at the final outlet of the inorganic separation membrane 2 is calculated.
The position of ΔP=(⅕)·PX·XCO2 shown by the short dashed line in
Further, in the separation method according to the present invention, it is preferred that the membrane separation is performed such that the carbon dioxide partial pressure difference ΔP [MPa] expressed by Formula (I) at the final outlet on the carbon dioxide non-permeation side becomes ⅗ or less of the carbon dioxide partial pressure (PX·XCO2) in the carbon dioxide non-permeation side pressure. When the relationship is expressed by equation, the following Formula (III-1) is obtained.
On the other hand, The position of ΔP=(⅗)·PX·XCO2 shown by the long dashed line in
When the relationship described above is summarized, the following Formula (IV-1) is obtained.
On the other hand,
In a case of XCO2>(PY/PX), the large or small of the driving force does not become problematic when the inorganic separation membrane 2 having relatively large ideal separation factor is used, therefore, in the present embodiment, it is preferred to be applied in a case where the carbon dioxide mole fraction at the final outlet on the carbon dioxide non-permeation side XCO2 is a ratio (PY/PX) or less of the carbon dioxide permeation side pressure PY to the carbon dioxide non-permeation side pressure PX (XCO2≤(PY/PX)).
Further, in the membrane separation of the separation method according to the present invention, in order to perform the membrane separation such that the carbon dioxide partial pressure difference ΔP is ⅕ or more of the carbon dioxide partial pressure on the carbon dioxide non-permeation side PX·XCO2, the ideal separation factor α of the inorganic separation membrane 2 to be used is preferably expressed by the following Formula (II). In Formula (II), α indicates the ideal separation factor of the inorganic separation membrane 2, PX indicates the carbon dioxide non-permeation side pressure [MPaA], XCO2 indicates the carbon dioxide mole fraction [−] at the final outlet on the carbon dioxide non-permeation side, PY indicates the carbon dioxide permeation side pressure [MPaA], and YCO2 indicates the carbon dioxide mole fraction [−] on the carbon dioxide permeation side.
In the same manner, in the membrane separation of the separation method according to the present invention, in order that the carbon dioxide partial pressure difference ΔP is ⅗ or less of the carbon dioxide partial pressure on the carbon dioxide non-permeation side PX·XCO2, the ideal separation factor α of the inorganic separation membrane 2 to be used is preferably expressed by the following Formula (III). In Formula (III), α, PX, XCO2, and PY are common to those in the above-described Formula (II).
The specifications of the calculation of Formula (II) and Formula (III) are as follows. Firstly, as to the membrane performance of the inorganic separation membrane 2, when the permeance of carbon dioxide is KCO2, and the permeance of methane is KCH4 (both unit are [mol/m2·s·Pa]), the ideal separation factors α=KCO2/KCH4, therefore, the following Formula (B1) is obtained.
[Mathematical Formula 13]
K
CH4
=K
CO2/α (B1)
As to the supply side, when the carbon dioxide mole fraction on the supply side is XCO2 [−], the methane mole fraction on the supply side is XCH4 [−], and carbon dioxide and methane are the main components, the relationship between XCO2 and XCH4 is the following Formula (B2).
[Mathematical Formula 14]
X
CO2
+X
CH4=1 (B2)
As to the permeation side, in the same manner as in the above, when the carbon dioxide mole fraction on the permeation side is YCO2 [−], the methane mole fraction on the permeation side is YCH4 [−], and carbon dioxide and methane are the main components, the relationship between YCO2 and YCH4 is the following Formula (B3).
[Mathematical Formula 15]
Y
CO2
+Y
CH4=1 (B3)
As to the gas permeation amount, when the carbon dioxide non-permeation side pressure (supply side pressure) is PX and the carbon dioxide permeation side pressure is PY (both are absolute pressure, and both units are MPaA), the permeation amount of carbon dioxide gas is TCO2 and the permeation amount of methane is TCH4 (both units are [mol/s]) in the inorganic separation membrane 2 in the separation membrane system 1, and the membrane area of the separation membrane is A [m2], the permeation amount of carbon dioxide gas TCO2 is expressed by the following Formula (B4) and the permeation amount of methane gas TCH4 is expressed by the following Formula (B5) (both units are [mol/s]).
[Mathematical Formula 16]
T
CO2
=K
CO2
A(PXXCO2−PYYCO2) (B4)
[Mathematical Formula 17]
T
CH4
=K
CH4
A(PXXCH4−PYYCH4) (B5)
Herein, the composition ratio of carbon dioxide gas and methane gas on the carbon dioxide permeation side at the final outlet (supply gas outlet) on the carbon dioxide non-permeation side, and the permeation amount of carbon dioxide gas and methane gas, which are equal to each other, accordingly the following Formula (B6) is derived.
[Mathematical Formula 18]
Y
CO2
/Y
CH4
=T
CO2
/T
CH4 (B6)
In addition, by assigning Formula (B1), Formula (B2), Formula (B3), Formula (B4), and Formula (B5) to Formula (B6), and by organizing for YCO2, the following Formula (B7) is obtained.
Further, the above-described Formula (II-1) is developed to obtain Formula (II-2), and the following Formula (B8) is obtained from the Formula (II-2) and the above-described Formula (B7).
Further, by assigning Formula (II-1) to the Formula (B8), and by organizing in relation to the ideal separation factor α, the following Formula (II) is obtained.
In the same manner, the above-described Formula (III-1) is developed to obtain Formula (III-2), and the following Formula (B9) is obtained from the (III-2) and the above-described Formula (B7).
In addition, by assigning Formula (III-1) to the Formula (B9), and by organizing in relation to the ideal separation factor α, the following Formula (III) is obtained.
In addition, when the above-described Formula (II) and Formula (III) are summarized for α, the following Formula (IV) is obtained.
Next, the relationship shown in
Ideal separation factor α: 5, 10, 25, 50, 100, 150, 200, 400, 600, 800, and 1000 (11 kinds from 5 to 1000)
Carbon dioxide non-permeation side pressure PX [MPaA]: 2.1, 4.1, and 6.1 (3 kinds from 2.1 to 6.1 MPaA)
Carbon dioxide permeation side pressure PY [MPaA]: 0.10, 0.15, 0.20, and 0.25 (4 kinds from 0.10 to 0.25 MPaA)
Supply gas carbon dioxide mole fraction X0 [−]: 0.10, 0.20, and 0.40 (3 kinds from 0.10 to 0.40)
Carbon dioxide mole fraction at the final outlet on the carbon dioxide non-permeation side (carbon dioxide mole fraction on the carbon dioxide non-permeation side) XCO2 [−]: 0.01, 0.02, and 0.03 (3 kinds from 0.01 to 0.03)
In addition, in the same manner as in
In addition, as to ΔP, from the calculation (simulation) results, the value at the final outlet on the carbon dioxide non-permeation side is extracted, and the relationship among the carbon dioxide partial pressure difference (ΔP), the membrane area relative value of an inorganic separation membrane, and the methane (CH4) recovery rate is shown in
Further, Correspondence Tables of each combination of parameters and the drawing numbers are shown in Tables 1 to 3. In Tables 1 to 3, the numerical values of “PY/PX” surrounded by thick lines (top of
(Correspondence Table)
(Correspondence Table)
As shown in
According to the present invention described above, the method for separating carbon dioxide is as follows. In a separation membrane system 1 provided with an inorganic separation membrane 2 that is permeated by carbon dioxide preferentially from a mixed gas containing methane and the carbon dioxide, the carbon dioxide is membrane-separated from the mixed gas such that the carbon dioxide partial pressure difference ΔP at the final outlet on the carbon dioxide non-permeation side is ⅕ or more of the carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2), therefore, the driving force that is a partial pressure difference of carbon dioxide between on the carbon dioxide non-permeation side and on the carbon dioxide permeation side is maintained, and further the membrane area of the inorganic separation membrane 2 to be used can be suppressed smaller, the carbon dioxide can be efficiently separated, and the cost is low.
Further, by setting ΔP to ⅗ or less of the carbon dioxide partial pressure PX·XCO2, the methane recovery rate is easily maintained in a relatively high state while maintaining the driving force that is a partial pressure difference (ΔP), accordingly, a technique in which the loss of methane to the permeation side is suppressed, and the recovery rate of methane is high is obtained.
In addition, the embodiment described above shows one embodiment of the present invention, the present invention is not limited to the above-described embodiment, and it goes without saying that modifications and improvements within the range in which the constitution of the present invention is provided and the object and effect of the present invention can be achieved are included in the content of the present invention. Further, there is no problem that even if other structures, shapes and the like are used as the specific structures, shapes and the like in performing the present invention within the range in which the object and effect of the present invention can be achieved. The present invention is not limited to the above-described each embodiment, and the modifications and improvements within the range in which the object of the present invention can be achieved are included in the present invention.
For example, in the above-described embodiment, as to the separation membrane system 1, the configuration shown in
In the embodiment described above, as a separation membrane system 1 in which the method for separating carbon dioxide according to the present invention is performed, a separation membrane system 1 configured by connecting an arbitrary number of inorganic separation membranes 2 in series is mentioned by using
Further, it has been described in the embodiment described above that carbon dioxide is membrane-separated from a mixed gas such that the carbon dioxide partial pressure difference ΔP at the final outlet on the carbon dioxide non-permeation side is ⅕ or more to ⅗ or less of the carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2) in the separation membrane system 1, but carbon dioxide may be membrane-separated from a mixed gas such that the carbon dioxide partial pressure difference ΔP is ⅕ or more of the carbon dioxide partial pressure on the carbon dioxide non-permeation side (PX·XCO2), for example, carbon dioxide may be membrane-separated from a mixed gas such that the carbon dioxide partial pressure difference ΔP is slightly larger than ⅗ of the carbon dioxide partial pressure (PX·XCO2).
In addition, the specific structures, shapes and the like in performing the present invention may be another structure or the like within the range in which the object of the present invention can be achieved.
The present invention can be advantageously used as a measure for separating carbon dioxide from a mixed gas such as a natural gas containing carbon dioxide and methane, and the industrial applicability is extremely high.
Number | Date | Country | Kind |
---|---|---|---|
2015-213263 | Oct 2015 | JP | national |
The present application is a continuation under 35 U.S.C. § 120 of PCT/JP2016/081453, filed Oct. 24, 2016, which is incorporated herein reference and which claimed priority to Japanese Application No. 2015-213263, filed Oct. 29, 2015, the entire content of which is also incorporated herein by reference. The present application likewise claims priority under 35 U.S.C. § 119 to Japanese Application No. 2015-213263, filed Oct. 29, 2015, the entire content of which is also incorporated herein by reference.
Number | Date | Country | |
---|---|---|---|
Parent | PCT/JP2016/081453 | Oct 2016 | US |
Child | 15966417 | US |