CO2 AND O2 REMOVER

Abstract

The present invention relates to the CO.sub.2 and O.sub.2 remover. The CO.sub.2 and O.sub.2 remover comprises 65 to 85 weight percent (wt. %) of a nickel oxide (NiO), 5 to 20 wt. % of a magnesium oxide (MgO), wherein the weight ratio of the nickel oxide and the magnesium oxide (NiO/MgO) is 4 to 11, and wherein the wt. % is based on the weight of the CO.sub.2 and O.sub.2 remover.

Claims

1. A CO.sub.2 and O.sub.2 remover comprising: 65 to 85 weight percent (wt. %) of a nickel oxide (NiO), 5 to 20 wt. % of a magnesium oxide (MgO), wherein the weight ratio of the nickel oxide and the magnesium oxide (NiO/MgO) is 4 to 11, and wherein the wt. % is based on the weight of the CO.sub.2 and O.sub.2 remover.

2. The CO.sub.2 and O.sub.2 remover of claim 1, wherein the CO.sub.2/O.sub.2 remover further comprises one or more of other metal oxide selected from the group consisting of an aluminum oxide (Al.sub.2O.sub.3), a silicon oxide (SiO.sub.2), an alkali metal oxide and a mixture thereof

3. The CO.sub.2 and O.sub.2 remover of claim 1, wherein the CO.sub.2 and O.sub.2 remover further comprises 1 to 30 wt. % of an aluminum oxide (Al.sub.2O.sub.3) based on the weight of the CO.sub.2 and O.sub.2 remover.

4. The CO.sub.2 and O.sub.2 remover of claim 1, wherein the CO.sub.2 and O.sub.2 remover further comprises 1 to 20 wt. % of a silicon oxide (SiO.sub.2) based on the weight of the CO.sub.2 and O.sub.2 remover.

5. The CO.sub.2 and O.sub.2 remover of claim 1, wherein the CO.sub.2 and O.sub.2 remover further comprises 0 to 2 wt. % of an alkali metal oxide based on the weight of the CO.sub.2 and O.sub.2 remover.

6. The CO.sub.2 and O.sub.2 remover of claim 1, wherein the CO.sub.2 and O.sub.2 remover comprises no alkali metal oxide.

7. The CO.sub.2 and O.sub.2 remover of claim 1, wherein specific surface area (S.sub.BET) of the CO.sub.2 and O.sub.2 remover is 10 to 1000 m.sup.2/g.

8. A method of manufacturing a CO.sub.2 and O.sub.2 remover comprising steps of: mixing a nickel compound and a magnesium compound, and calcining the mixture to form the CO.sub.2 and O.sub.2 remover, wherein the CO.sub.2 and O.sub.2 remover comprises 65 to 85 weight percent (wt. %) of a nickel oxide (NiO), 5 to 20 wt. % of a magnesium oxide (MgO), wherein the weight ratio of the nickel oxide and the magnesium oxide (NiO/MgO) is 4 to 11, wherein the wt. % is based on the weight of the CO.sub.2 and O.sub.2 remover.

9. The method of manufacturing a CO.sub.2 and O.sub.2 remover of claim 8, wherein the method further comprises a step of adding an aluminum compound to the mixture of a nickel compound and a magnesium compound before the step of calcining or after the step of calcining.

10. The method of manufacturing a CO.sub.2 and O.sub.2 remover of claim 8, wherein the method further comprises a step of shaping the mixture of the nickel compound and the magnesium compound.

11. A method of removing CO.sub.2 and O.sub.2 from air comprising steps of: placing a CO.sub.2 and O.sub.2 remover in a container, wherein the CO.sub.2 and O.sub.2 remover comprises 65 to 85 weight percent (wt. %) of a nickel oxide (NiO), 5 to 20 wt. % of a magnesium oxide (MgO), wherein the weight ratio of the nickel oxide and the magnesium oxide (NiO/MgO) is 4 to 11, and wherein the wt. % is based on the weight of the CO.sub.2 and O.sub.2 remover; and passing air through the container.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0009] FIG. 1 shows an example of the cylindrical CO2/O2 remover 10 having a round cross section.

[0010] FIG. 2 shows an example of the cylindrical CO2/O2 remover 20 with a trilobed cross section.

DETAILED DESCRIPTION OF THE INVENTION

[0011] The CO.sub.2/O.sub.2 remover and the method of manufacturing thereof are explained below.

[0012] The CO.sub.2/O.sub.2 remover comprises 65 to 85 weight percent (wt. %) of a nickel oxide (NiO), 5 to 20 wt. % of a magnesium oxide (MgO) based on the weight of the CO.sub.2/O.sub.2 remover.

[0013] The NiO is 66.5 wt. % or more in an embodiment, 67.5 wt. % or more in another embodiment, 68.5 wt. % or more in another embodiment, 69 wt. % or more in another embodiment, 70.5 wt. % or more in another embodiment, 71.2 wt. % or more in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover. The NiO is 83.5 wt. % or less in an embodiment, 82.1 wt. % or less in another embodiment, 80.5 wt. % or less in another embodiment, 78.6 wt. % or less in another embodiment, 76 wt. % or less in another embodiment, 74.5 wt. % or less in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover.

[0014] The MgO is 5.5 wt. % or more in an embodiment, 6.2 wt. % or more in another embodiment, 7.5 wt. % or more in another embodiment, 7.9 wt. % or more in another embodiment, 8.9 wt. % or more in another embodiment, 9.9 wt. % or more in another embodiment, 10.5 wt. % or more in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover. The MgO is 19.2 wt. % or less in an embodiment, 18.1 wt. % or less in another embodiment, 17.5 wt. % or less in another embodiment, 16.3 wt. % or less in another embodiment, 15.5 wt. % or less in another embodiment, 14.8 wt. % or less in another embodiment, 13.2 wt. % or less in another embodiment, 12.5 wt. % or less in another embodiment, 11.1 wt. % or less in another embodiment, 9.9 wt. % or less in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover.

[0015] The weight ratio of NiO and MgO (NiO/MgO) is 4 to 11. The weight ratio of NiO and MgO (NiO/MgO) is 4.5 or more in an embodiment, 5.1 or more in another embodiment, 5.7 or more in another embodiment, 6.1 or more in another embodiment, 6.9 or more in another embodiment, 7.5 or more in another embodiment, 8.1 or more in another embodiment. The weight ratio of NiO and MgO (NiO/MgO) is 10.5 or less in another embodiment, 9.8 or less in another embodiment, 5.7 or less in another embodiment, 9 or less in another embodiment, 8.2 or less in another embodiment, 7.5 or less in another embodiment, 6.8 or less in another embodiment. The CO.sub.2/O.sub.2 remover comprising NiO and MgO within the range at the weight ratio above could sufficiently remove both CO.sub.2 and O.sub.2.

[0016] The CO.sub.2/O.sub.2 remover further comprises one or more of other metal oxide selected from the group consisting of a silicon oxide (SiO.sub.2), an aluminum oxide (Al.sub.2O.sub.3), a sodium oxide (Na.sub.2O) and a mixture thereof in an embodiment. The CO.sub.2/O.sub.2 remover further comprises one or more of other metal oxide selected from the group consisting of a silicon oxide (SiO.sub.2), an aluminum oxide (Al.sub.2O.sub.3) and a mixture thereof in another embodiment.

[0017] The CO.sub.2/O.sub.2 remover comprises SiO.sub.2 other than NiO and MgO in another embodiment. The SiO.sub.2 is 1 wt. % or more in an embodiment, 2.2 wt. % or more in another embodiment, 2.9 wt. % or more in another embodiment, 3.6 wt. % or more in another embodiment, 4.5 wt. % or more in another embodiment, 5.2 wt. % or more in another embodiment, 6.9 wt. % or more in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover. SiO.sub.2 is 20 wt. % or less in an embodiment, 17.2 wt. % or less in another embodiment, 13.5 wt. % or less in another embodiment, 10.3 wt. % or less in another embodiment, 8.5 wt. % or less in another embodiment, 6.4 wt. % or less in another embodiment, 5.2 wt. % or less in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover.

[0018] The CO.sub.2/O.sub.2 remover comprises Al.sub.2O.sub.3 other than NiO and MgO in an embodiment. The Al.sub.2O.sub.3 is 1 wt. % or more in an embodiment, 3.2 wt. % or more in another embodiment, 5.9 wt. % or more in another embodiment, 7.2 wt. % or more in another embodiment, 9.5 wt. % or more in another embodiment, 10.1 wt. % or more in another embodiment, 11.2 wt. % or more in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover. The Al.sub.2O.sub.3 is 30 wt. % or less in an embodiment, 26.3 wt. % or less in another embodiment, 22.5 wt. % or less in another embodiment, 18.3 wt. % or less in another embodiment, 15.5 wt. % or less in another embodiment, 12.8 wt. % or less in another embodiment, 11.6 wt. % or less in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover.

[0019] The CO.sub.2/O.sub.2 remover comprises an alkali metal oxide other than NiO and MgO in an embodiment. The alkali metal oxide is selected from the group consisting of a sodium oxide (Na.sub.2O), a potassium oxide (K.sub.2O), a lithium oxide (Li.sub.2O) and a combination thereof in another embodiment. The alkali metal oxide comprises a sodium oxide (Na.sub.2O) in another embodiment. The alkali metal oxide is 0.01 wt. % or more in an embodiment, 0.05 wt. % or more in another embodiment, 0.09 wt. % or more in another embodiment, 0.1 wt. % or more in another embodiment, 0.24 wt. % or more in another embodiment, 0.33 wt. % or more in another embodiment, 0.42 wt. % or more in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover. The alkali metal oxide is 2 wt. % or less in an embodiment, 1.9 wt. % or less in another embodiment, 1.2 wt. % or less in another embodiment, 0.8 wt. % or less in another embodiment, 0.6 wt. % or less in another embodiment, based on the weight of the CO.sub.2/O.sub.2 remover. The CO.sub.2/O.sub.2 remover could comprise no alkali metal oxide or Na.sub.2O in another embodiment.

[0020] The CO.sub.2/O.sub.2 remover composition described herein, including those listed in Table I, are not limiting; it is contemplated that one of ordinary skill in the art of chemistry could make minor substitutions or additional ingredients and not substantially change the desired properties of the CO.sub.2/O.sub.2 remover. For example, substitutions such as oxides of iron (Fe), calcium (Ca), titan (Ti), cerium (Ce), zinc (Zn), zirconium (Zr) in amount of 0.001 to 3.0 wt. % based on the weigh of the CO.sub.2/O.sub.2 remover may be used either individually or in combination to achieve similar performance. The CO.sub.2/O.sub.2 remover composition can be determined by a fluorescent X-ray analysis (XRF analysis) about the CO.sub.2/O.sub.2 remover.

[0021] The shape of the CO.sub.2/O.sub.2 remover is not limited. The CO.sub.2/O.sub.2 remover can be any shape as long as it generates sufficient removal capacity and strength as a CO.sub.2/O.sub.2 remover. The CO.sub.2/O.sub.2 remover is particle in an embodiment. The CO.sub.2/O.sub.2 remover is cylindrical or spherical in another embodiment. Cross section of the cylindrical CO.sub.2/O.sub.2 remover is selected from the group consisting of round, ellipse, polygon, rectangle and polylob in an embodiment. Cross section of the cylindrical CO.sub.2/O.sub.2 remover is round, ellipse or polylobe in another embodiment, polylobe in another embodiment, trilobe in another embodiment.

[0022] An example of the cylindrical CO.sub.2/O.sub.2 remover 10 cross-sectionally round is shown in FIG. 1. Diameter 12 of the cylindrical CO.sub.2/O.sub.2 remover 10 is 0.5 to 10 mm in an embodiment, 0.8 to 8.7 mm in another embodiment, 1 to 5.7 mm in another embodiment, 1.2 to 3.3 mm in another embodiment. Length 13 of the cylindrical CO.sub.2/O.sub.2 remover 10 is 0.5 to 30 mm in an embodiment, 1.2 to 21 mm in another embodiment, 2.5 to 16 mm in another embodiment, 3.2 to 10 mm in another embodiment. The diameter of the ellipse and rectangle cross-section is the major axis. Diameter of the cross-section of polylobe, polygon is diameter of the circumcircle. An example of the cylindrical CO.sub.2/O.sub.2 remover 20 cross-sectionally trilobe is shown in FIG. 2. The circumcircle 21 of the trilobe cross-section is taken for the diameter of the cylindrical CO.sub.2/O.sub.2 remover 20. Diameter 22 of the trilobe CO.sub.2/O.sub.2 remover 20 is 0.5 to 10 mm in an embodiment, 0.8 to 8.7 mm in another embodiment, 1 to 5.7 mm in another embodiment, 1.2 to 3.3 mm in another embodiment. Length 23 of the trilobe cylindrical CO.sub.2/O.sub.2 remover 20 is 0.5 to 30 mm in an embodiment, 1.2 to 21 mm in another embodiment, 2.5 to 16 mm in another embodiment, 3.2 to 10 mm in another embodiment.

[0023] The CO.sub.2/O.sub.2 remover is porous in an embodiment. The pore volume is 0.05 mm.sup.3/g to 5.0 mm.sup.3/g in an embodiment. The pore volume can be measured with an automatic pore size distribution measure instrument for example BELSORP-mini-II from MicrotracBEL Corporation. Surface area (S.sub.BET) of the CO.sub.2/O.sub.2 remover is 10 to 1000 m.sup.2/g in an embodiment, 32 to 800 m.sup.2/g in another embodiment, 58 to 645 m.sup.2/g in another embodiment, 68 to 500 m.sup.2/g in another embodiment, 80 to 320 m.sup.2/g in another embodiment, 85 to 240 m.sup.2/g in another embodiment, 100 to 200 m.sup.2/g in another embodiment. The surface area could be measured by a BET method (a single-point method) with a N.sub.2 gas absorption at a liquid nitrogen temperature. A surface area analyzer such as Macsorb® Model-1210 from MOUNTECH Co., Ltd. could be used.

[0024] The CO.sub.2/O.sub.2 remover is made by a precipitation method or a dry method in an embodiment. A Ni compound, a Mg compound and optionally a Si compound, an Al compound and/or a Na compound are prepared. The compounds are mixed and calcined to form the CO.sub.2/O.sub.2 remover. The Al compound can be added to the mixture of the Ni compound and the Mg compound before the step of calcining or after the step of calcining in an embodiment.

[0025] For the raw materials of the CO.sub.2/O.sub.2 remover such as the compound of Ni, Mg, Al, Si and Na, any compound which provides the metal oxide thereof after calcination can be used.

[0026] The Ni compound could be an oxide, a salt or a mixture thereof. The Ni compound could be selected from the group consisting of a nickel oxide, a nickel nitrate, a nickel nitrite, a nickel hydrosulfate and a combination thereof in an embodiment.

[0027] The Mg compound could be an oxide, a salt or a mixture thereof. The Mg compound could be selected from the group consisting of an oxide, a magnesium nitrate, a magnesium nitrite, a magnesium hydrosulfate and a combination thereof in an embodiment.

[0028] The Si compound could be selected from the group consisting of a silica, a diatom earth, a liquid glass and a combination thereof in an embodiment.

[0029] The Al compound could be selected from the group consisting of a boehmite, an alumina sol and a combination thereof in an embodiment.

[0030] The Al compound could also function as a binder for the Ni compound and the Mg compound. As the Al compound could function as a binder of the precipitate, the Al compound could be separately mixed with the precipitate in another embodiment.

[0031] The Na compound could be a sodium carbonate in an embodiment.

[0032] The metal compounds could be mixed through a precipitation method where a solution dissolving the Ni compound and the Mg compound is prepared in an embodiment. The Ni compound and the Mg compound can be soluble salts, such as nitrates, nitrites and hydrosulfate in another embodiment. The Ni compound is nickel nitrate in another embodiment. The Mg compound is magnesium nitrate in another embodiment. The Si compound and/or the Al compound could be added to dissolve in the solution in another embodiment. The Si compound could be dissolved in the solution in another embodiment. The solvent is a water in an embodiment. The solution is heated at 40° C. or higher for 1 hour or more in an embodiment to generate a precipitate. The precipitate was taken out by filtering in an embodiment. The precipitate is powder or particle in an embodiment. The precipitate is optionally mixed with the Si component and/or the Al component in another embodiment.

[0033] The metal compound mixture is calcined. The calcination is carried out after the step of shaping the metal compound mixture in another embodiment. The calcination temperature could be 100 to 900° C. in an embodiment, 120 to 680° C. in another embodiment, 180 to 500° C. in another embodiment, 200 to 400° C. in another embodiment. The calcination time is 30 minutes or more in an embodiment, 1 hour or more in another embodiment. The calcination time is 5 hours or less in an embodiment, 3 hours or less in another embodiment.

[0034] The mixture of the metal compounds can be shaped in a desired form in an embodiment. The shaping method is not limited but in an embodiment the mixture of the metal compounds is shaped by extruding or molding.

[0035] The shaped metal compound mixture could be calcined in an embodiment. The precipitate optionally mixed with the Si component and/or the Al component is calcined in an embodiment.

[0036] The CO.sub.2/O.sub.2 remover is reduced by exposing to a hydrogen gas in an embodiment. The hydrogen gas is a gas flow of 300 to 550° C. for 5 to 30 hours in an embodiment. After the reduction, an oxide layer is formed at the surface of the CO.sub.2/O.sub.2 remover for stabilization by for example exposing to a gas containing O.sub.2 in an embodiment.

[0037] In the precipitation method, the solution can be separately prepared as an acid solution and an alkali solution in an embodiment. The acid solution is prepared by dissolving the Ni compound and the Mg compound in a solution in an embodiment. An alkali solution is prepared by dissolving the additional metal compound such as a Na compound in a solution in an embodiment. The Si compound could be dissolved in the acid solution in an embodiment. The acid solution is incrementally feed to the alkali solution until the mixed solution indicated about pH 7 in an embodiment. The precipitate from the mixed solution is taken out and get calcined.

[0038] In another embodiment, a method of manufacturing a CO.sub.2 and O.sub.2 remover comprises steps of: mixing a nickel compound and a magnesium compound, shaping the mixture of the nickel compound and the magnesium compound, and calcining the shaped mixture.

[0039] In another embodiment, a method of manufacturing a CO.sub.2 and O.sub.2 remover comprises steps of: mixing a nickel compound and a magnesium compound, calcining the mixture of the nickel compound and the magnesium compound, and shaping the calcined mixture.

[0040] The CO.sub.2/O.sub.2 remover can be also prepared by a dry method in another embodiment. The Ni compound and the Mg compound are mixed and calcined in another embodiment.

[0041] The CO.sub.2/O.sub.2 remover is used any places where CO.sub.2 and O.sub.2 are undesired in an atmosphere. For example, the CO.sub.2/O.sub.2 remover is applied to a gas purification system at a semiconductor manufacturing site.

EXAMPLE

Example 1

[0042] The CO.sub.2/O.sub.2 remover was prepared by the following method. An acid solution was prepared by dissolving 7.5 kg of nickel nitrate, 1.6 kg of magnesium nitrate and 0.3 kg of diatom earth in 14.7 kg of ion-exchanged water. Separately, an alkali solution was prepared by dissolving 3.9 kg of sodium carbonate in 17.4 kg of pure water. The acid solution was feed to the alkali solution until the mixed solution indicated neutrality. The generated precipitate was taken out by filtering and washing. The precipitate was dried and calcinated at 350° C. for two hour. The precipitate powder and boehmite were mixed at a weight ratio (precipitate powder:boehmite) of 9:1. The precursor CO.sub.2/O.sub.2 remover was formed by extruding the powder mixture with a vertical extruder. The extruded precursor of the CO.sub.2/O.sub.2 remover was cross-sectionally trilobe shape 20 with 1.6 mm of diameter 21 and about 7 mm of length 22 (FIG. 2).

[0043] The CO.sub.2/O.sub.2 remover of 300 cm.sup.3 was filled in a quartz tube (40 mm inner diameter and 950 mm long) having an inlet and an outlet. The CO.sub.2/O.sub.2 remover reduced by exposing to a pure hydrogen gas. Then the hydrogen gas switched to a nitrogen gas after cooling down to room temperature. After purging the hydrogen gas, a nitrogen gas containing oxygen was flown in the tube to stabilize the CO.sub.2/O.sub.2 remover by making the oxide layer at the surface.

[0044] The surface area (SA.sub.BET) was about 150 m.sup.2/g measured by Macsorb® Model-1210 from MOUNTECH Co., Ltd.

[0045] The composition of the formed CO.sub.2/O.sub.2 remover was analyzed by a X-ray fluorescence spectrometer (XRF, Supermini-200, RIGAKU Corporation).

Example 2

[0046] The CO.sub.2/O.sub.2 remover was formed in the same manner of Example 1 except that magnesium nitrate hexahydrate was 2.43 kg, and silica was 0.14 kg.

[0047] The surface area (SA.sub.BET) was about 150 m.sup.2/g.

Comparative Example 1

[0048] The CO.sub.2/O.sub.2 remover was formed in the same manner of Example 1 except for the composition. The compositions of the CO.sub.2/O.sub.2 remover are shown in Table 1. The surface area (SA.sub.BET) was about 150 m.sup.2/g.

[0049] Measurement

[0050] CO.sub.2 Removal Amount

[0051] A quartz tube (inner diameter 20 mm, height 500 mm) was charged with 40 cm.sup.3 of the CO.sub.2/O.sub.2 remover obtained above. The tube had an inlet at the top and an outlet at the bottom. A reduction was conducted to remove the oxide layer. After the reduction, a 30 ppm CO.sub.2 gas (CO.sub.2/N.sub.2) flowed from the inlet to the outlet through the CO.sub.2/O.sub.2 remover at SV of about 3,500 h.sup.−1. The CO.sub.2 gas flow stopped when the CO.sub.2 concentration at the outlet increased from zero to 0.5 ppm.

[0052] The CO.sub.2 concentration of the outlet gas was measured with a gas chromatograph analyzer with a flame-ionization-detector (FID) and a methanizer (GC-8A/MTN-1, SHIMADZU CORPORATION).

[0053] O.sub.2 Removal Amount

[0054] A 200 ppm O.sub.2 gas (air/N.sub.2) flowed from the inlet to the outlet through the CO.sub.2/O.sub.2 remover at SV of about 3,500 h.sup.−1. The O.sub.2 gas flow stopped when the O.sub.2 concentration at the outlet increased from zero to 7.0 ppm. The O.sub.2 concentration of the outlet gas was measured with a trace oxygen analyzer (Model 1000-RS, Advanced Micro Instruments, Inc.).

[0055] The “CO.sub.2 absorption” and “O.sub.2 absorption” were calculated by the equations below.

CO.sub.2 removal (m.sup.3/kg)=CO.sub.2 gas flow rate (m.sup.3/h)×CO.sub.2 gas flow time (h)×CO.sub.2 concentration 30 ppm/the remover weight (kg)

O.sub.2 removal (m.sup.3/kg)=O.sub.2 gas flow rate (m.sup.3/h)×O.sub.2 gas flow time (h)×O.sub.2 concentration 200 ppm/the remover weight (kg)

[0056] Results are shown in Table 1 below. The CO.sub.2 removal was sufficiently over 1.6×10.sup.−3 m.sup.3/kg and the O.sub.2 removal was sufficiently over 20×10.sup.−3 m.sup.3/kg in Example (Ex.) 1 and 2. The O.sub.2 removal was insufficiently 14×10.sup.−3 m.sup.3/kg in Comparative Example (Com. Ex.) 1.

TABLE-US-00001 TABLE 1 CO.sub.2 O.sub.2 removal × removal × Composition (wt. %) NiO/ 10.sup.3 10.sup.3 NiO MgO SiO.sub.2 Al.sub.2O.sub.3 Na.sub.2O MgO m.sup.3/kg m.sup.3/kg Ex. 1 72.8 8.2 7.6 10.8 0.5 8.8 1.6 26.6 Ex. 2 72.3 11.4 4.2 12.0 0.0 6.3 3.6 20.2 Com. 63.4 15.8 8.0 12.4 0.3 4.0 4.8 14.0 Ex. 1