JP2017039633A - Zirconium hydroxide mesoporous body having carbon dioxide adsorptivity, manufacturing method therefor and carbon dioxide adsorbent consisting of zirconium hydroxide mesoporous body - Google Patents
Zirconium hydroxide mesoporous body having carbon dioxide adsorptivity, manufacturing method therefor and carbon dioxide adsorbent consisting of zirconium hydroxide mesoporous body Download PDFInfo
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- IVORCBKUUYGUOL-UHFFFAOYSA-N 1-ethynyl-2,4-dimethoxybenzene Chemical compound COC1=CC=C(C#C)C(OC)=C1 IVORCBKUUYGUOL-UHFFFAOYSA-N 0.000 title claims abstract description 95
- 239000003463 adsorbent Substances 0.000 title claims abstract description 29
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 title claims description 36
- 238000004519 manufacturing process Methods 0.000 title claims description 19
- 229910002092 carbon dioxide Inorganic materials 0.000 title claims description 18
- 239000001569 carbon dioxide Substances 0.000 title claims description 17
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 78
- 239000007787 solid Substances 0.000 claims abstract description 38
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 16
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- 238000000926 separation method Methods 0.000 claims description 13
- UJVRJBAUJYZFIX-UHFFFAOYSA-N nitric acid;oxozirconium Chemical compound [Zr]=O.O[N+]([O-])=O.O[N+]([O-])=O UJVRJBAUJYZFIX-UHFFFAOYSA-N 0.000 claims description 4
- WRAGBEWQGHCDDU-UHFFFAOYSA-M C([O-])([O-])=O.[NH4+].[Zr+] Chemical compound C([O-])([O-])=O.[NH4+].[Zr+] WRAGBEWQGHCDDU-UHFFFAOYSA-M 0.000 claims description 3
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 abstract description 43
- 229910021536 Zeolite Inorganic materials 0.000 abstract description 42
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 abstract description 42
- 238000001556 precipitation Methods 0.000 abstract description 3
- OERNJTNJEZOPIA-UHFFFAOYSA-N zirconium nitrate Chemical compound [Zr+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O OERNJTNJEZOPIA-UHFFFAOYSA-N 0.000 abstract 2
- 239000000243 solution Substances 0.000 description 38
- 238000002336 sorption--desorption measurement Methods 0.000 description 21
- 150000001412 amines Chemical class 0.000 description 19
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 18
- 239000011148 porous material Substances 0.000 description 14
- 238000011084 recovery Methods 0.000 description 14
- QBHQQYMEDGADCQ-UHFFFAOYSA-N oxozirconium(2+);dinitrate;dihydrate Chemical compound O.O.[Zr+2]=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O QBHQQYMEDGADCQ-UHFFFAOYSA-N 0.000 description 12
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- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 4
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
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- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 230000000274 adsorptive effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
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- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 1
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
- Y02C20/00—Capture or disposal of greenhouse gases
- Y02C20/40—Capture or disposal of greenhouse gases of CO2
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/151—Reduction of greenhouse gas [GHG] emissions, e.g. CO2
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- Separation Of Gases By Adsorption (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
本発明は、特定のＣＯ2吸着性を有する水酸化ジルコニウムメソ多孔体、該水酸化ジルコニウムメソ多孔体からなるＣＯ2吸着剤、該水酸化ジルコニウムメソ多孔体の製造方法、及び、該ＣＯ2吸着剤を用いたＣＯ2吸脱着方法に関する。 The present invention, zirconium hydroxide mesoporous material having a specific CO 2 adsorptive, CO 2 adsorbent consisting of water zirconium oxide mesoporous material, a method of manufacturing a water-zirconium oxide mesoporous material, and, the CO 2 adsorption The present invention relates to a CO 2 adsorption / desorption method using an agent.
火力発電所、石炭ガス化複合発電施設（IGCC：Integrated Gasification Combined Cycle）、製鉄所、化学プラント等から大量に排出される二酸化炭素（以下「ＣＯ2」ということもある）は、地球温暖化の大きな要因になっている。ＣＯ2回収・貯留技術（CCS: Carbon dioxide Capture and Storage）は、ＣＯ2の大気中への排出削減効果が大きいことから、地球温暖化対策への選択肢の一つとして期待されている。
従来のＣＯ2分離・回収技術として、アミン溶液を用いた化学吸収法が挙げられる。アミン溶液はＣＯ2と化学反応を起こして強く結合する性質があり、排ガス中のＣＯ2とアミン溶液を吸収塔内で接触させることでＣＯ2を選択的に吸収することができる。ＣＯ2を吸収したアミン溶液は、再生塔内で高温加熱によってＣＯ2とアミン溶液に分離され、その後ＣＯ2だけを再生塔頂部から回収して濃縮する（特許文献１、２）。
Carbon dioxide (hereinafter sometimes referred to as “CO 2 ”) emitted in large quantities from thermal power plants, integrated gasification combined cycle (IGCC), steelworks, chemical plants, etc. It is a big factor. CO 2 capture and storage (CCS: Carbon dioxide Capture and Storage ) , since emission reduction effect on the atmospheric CO 2 is large, it is expected as an option to global warming.
As a conventional CO 2 separation / recovery technique, there is a chemical absorption method using an amine solution. The amine solution has a property of causing a chemical reaction with CO 2 and binding strongly, and CO 2 can be selectively absorbed by bringing CO 2 in the exhaust gas into contact with the amine solution in the absorption tower. The amine solution that has absorbed CO 2 is separated into CO 2 and an amine solution by high-temperature heating in the regeneration tower, and then only CO 2 is recovered from the top of the regeneration tower and concentrated (
しかしながら、アミン溶液を用いた化学吸収法（従来技術）には、次のような問題点が存在する。
（１）強く化学結合したＣＯ2とアミン溶液を加熱分離する際に大量の熱エネルギーが必要となるため、ＣＯ2分離・回収プロセスの高コスト化が不可避である。
（２）アミン溶液は、ＣＯ2分離・回収工程において熱劣化や酸素劣化等を起こすため短寿命であるし、アミン溶液の性能劣化によってＣＯ2回収量が著しく低下する。また劣化アミン溶液の発生に伴い、劣化アミン溶液の廃液処理と補填が必要となり、これらがプロセスの煩雑化と高コスト化に繋がる。
（３）アミン溶液は反応性に富むが、一方で毒性や腐食性も高く、設備腐食や高環境負荷発生の原因となっている。加えて、アミン溶液は可燃性でもあるため、設備内での爆発や火災の危険性を伴う。
However, the chemical absorption method (prior art) using an amine solution has the following problems.
(1) Since a large amount of heat energy is required when heat-separating strongly chemically bound CO 2 and an amine solution, it is inevitable to increase the cost of the CO 2 separation / recovery process.
(2) The amine solution has a short life because it causes thermal deterioration, oxygen deterioration, and the like in the CO 2 separation / recovery process, and the CO 2 recovery amount is remarkably reduced due to the performance deterioration of the amine solution. Further, with the generation of the deteriorated amine solution, it is necessary to treat and supplement the deteriorated amine solution, which leads to complicated processes and high costs.
(3) The amine solution is rich in reactivity, but on the other hand, it is highly toxic and corrosive, causing equipment corrosion and high environmental load. In addition, the amine solution is also flammable, causing explosions and fire in the facility.
上記の問題を回避するために、近年、化学吸収法に代替するＣＯ2分離・回収技術の開発が求められており、固体吸着剤を利用したＣＯ2分離・回収技術の開発について検討されている。
固体吸着剤は、ナノスケールの細孔構造を持つ多孔質材料であり、高い細孔表面積を有する。この細孔表面にＣＯ2吸着能を付与することで、多孔質材料にＣＯ2を吸着させることができる。アミン溶液に比べて固体吸着剤の優位な点は、固体吸着剤の細孔表面に吸着したＣＯ2を脱着する際に加熱操作を必要とせず、ＣＯ2導入圧(10〜3000kPa)下での加圧・減圧操作(圧力スイング吸脱着法)のみによってＣＯ2の吸脱着が可能となることである。また、固体吸着剤はアミン溶液に比べて毒性、腐食性、可燃性が低く、安全性とハンドリング性に優れた低環境負荷な材料である。アミン溶液の代わりに固体吸着剤を用いることで、ＣＯ2分離・回収プロセスの低コスト化と省エネルギー化が期待される。
To avoid the above problems, in recent years, the chemical absorption method has been required for the development of alternative to CO 2 separation and recovery techniques are being considered for the development of CO 2 separation and recovery technique utilizing solid adsorbent .
The solid adsorbent is a porous material having a nanoscale pore structure and has a high pore surface area. By imparting CO 2 adsorption capacity in this pore surfaces, it can be adsorbed CO 2 in porous material. The advantage of the solid adsorbent compared to the amine solution is that no heating operation is required when desorbing CO 2 adsorbed on the pore surface of the solid adsorbent, and under the CO 2 introduction pressure (10 to 3000 kPa). CO 2 can be adsorbed and desorbed only by pressurizing and depressurizing operations (pressure swing adsorption / desorption method). The solid adsorbent is a low environmental load material that is less toxic, corrosive, and flammable than an amine solution, and is excellent in safety and handling. By using a solid adsorbent instead of an amine solution, cost reduction and energy saving of the CO 2 separation / recovery process are expected.
固体吸着剤に要求される性能を以下に記す。
（１）ＣＯ2吸着能を有し、既存のゼオライト13Xとほぼ同等かそれ以上の高いＣＯ2回収量を有する材料であること。
（２）ＣＯ2分離・回収の際に熱エネルギーを必要としない、再生利用可能な材料であること。このとき、室温(25℃)・ＣＯ2導入圧(10〜3000kPa)下での加圧・減圧操作(圧力スイング吸脱着法)のみによってＣＯ2の吸脱着が可能であること。
（３）低コストで合成可能な材料であること。また、合成手法が簡便であること。
（４）毒性、腐食性、可燃性等が低く、環境負荷の低い材料であること。
（５）材料劣化を起こさない、高い耐久性を有すること。
The performance required for the solid adsorbent is described below.
(1) The material has a CO 2 adsorption capacity and a high CO 2 recovery amount that is almost equal to or higher than that of the existing
(2) Recyclable material that does not require heat energy for CO 2 separation and recovery. At this time, room temperature (25 ° C.), CO 2 introduction pressure (10～3000KPa) pressurization and depressurization under (pressure swing adsorption-desorption method) it is possible adsorption and desorption of CO 2 by only.
(3) The material can be synthesized at low cost. Also, the synthesis method should be simple.
(4) The material must have low environmental impact, such as low toxicity, corrosivity, and flammability.
(5) To have high durability without causing material deterioration.
上記の性能のうちのいくつかを満足する固体吸着剤として、ゼオライトが挙げられる（非特許文献１，２参照）。
ゼオライトは、ミクロスケールの規則的な細孔を有し、耐久性に優れ、同時に毒性、腐食性や可燃性が低く、低環境負荷で安全性の高い多孔質材料であって、その細孔内表面にＣＯ2吸着能を有するため、加熱操作を必要とせず、加圧・減圧操作のみでＣＯ2の吸脱着が可能となる。
しかしながら、ゼオライトを用いてＣＯ2分離・回収する際に、以下の問題点がある。
（１）ゼオライトは、特にIGCCのような1000kPa以上の高圧領域においてはＣＯ2回収量が不十分であり、例えば、25℃、1600kPaの環境下において、ゼオライトは約3.6mmol/mLのＣＯ2回収量を示すが、これよりも高いＣＯ2回収量を有する固体吸着剤の開発が必要である。
（２）ゼオライトは、真密度が低く、重量の軽い材料であるため、これを吸着塔に充填して排ガスを流通した際、吸着塔内で固体吸着剤の流動化が起こり、固体吸着剤のＣＯ2吸着量が低下する。また、固体吸着剤の流動化を防止するため造粒が必要となり、これによって最終的な固体吸着剤のＣＯ2吸着量が著しく低下する。
（３）ゼオライトの場合、圧力を10-3000kPaで吸脱着させた際の有効吸着量が低い（約1.5mmol/mL）。
（４）実際の排ガス中には微量水分が含まれており、ゼオライトの場合、水の阻害によってＣＯ2吸着性能が著しく低下する。このため、ゼオライトを用いる場合は、あらかじめ除湿プロセスを導入し、400℃以上の高温でゼオライトに吸着した水分を除去する必要がある。このため除湿プロセスの導入は、分離回収に係るエネルギー消費量を増大させる。
As a solid adsorbent that satisfies some of the above-mentioned performances, zeolite can be cited (see Non-Patent
Zeolite is a porous material with regular micro-scale pores, excellent durability, and at the same time low toxicity, corrosiveness and flammability, low environmental load and high safety. because having a CO 2 adsorption capacity to the surface, without the need for heating operation, it is possible to adsorption and desorption of CO 2 only pressure-vacuum operation.
However, when CO 2 is separated and recovered using zeolite, there are the following problems.
(1) The amount of CO 2 recovered from zeolite is particularly insufficient in the high pressure region of 1000 kPa or more such as IGCC. For example, the zeolite recovers about 3.6 mmol / mL of CO 2 in an environment of 25 ° C. and 1600 kPa. There is a need for the development of solid adsorbents with higher CO 2 recovery than indicated.
(2) Since zeolite is a material with a low true density and a light weight, when this is filled in an adsorption tower and the exhaust gas is circulated, fluidization of the solid adsorbent occurs in the adsorption tower. The amount of CO 2 adsorption decreases. In addition, granulation is required to prevent fluidization of the solid adsorbent, which significantly reduces the CO 2 adsorption amount of the final solid adsorbent.
(3) In the case of zeolite, the effective adsorption amount when adsorbed and desorbed at a pressure of 10 to 3000 kPa is low (about 1.5 mmol / mL).
(4) The actual exhaust gas contains a trace amount of water, and in the case of zeolite, the CO 2 adsorption performance is significantly reduced due to water inhibition. For this reason, when using zeolite, it is necessary to introduce a dehumidification process in advance to remove moisture adsorbed on the zeolite at a high temperature of 400 ° C. or higher. For this reason, the introduction of the dehumidification process increases the energy consumption for separation and recovery.
上述したとおり、固体吸着剤を利用したＣＯ2分離・回収技術も検討されているが、ゼオライトを含め、既存のアミン溶液に代替できるような固体吸着剤は未だ見つかっていない。 As described above, CO 2 separation / recovery technology using a solid adsorbent has also been studied, but no solid adsorbent that can be substituted for an existing amine solution, including zeolite, has yet been found.
本発明は、こうした現状を鑑みてなされたものであって、従来のゼオライト13Xとほぼ同等かそれ以上の高いＣＯ2吸着量を有するＣＯ2吸着剤として有用な水酸化ジルコニウムメソ多孔体を提供することを課題とする。
また、本発明は、所定のＣＯ2吸着量を有する水酸化ジルコニウムメソ多孔体からなるＣＯ2吸着剤を提供することを追加的な課題とする。
また、本発明は、従来法よりも簡便で、且つ加熱することなく製造することができる水酸化ジルコニウムメソ多孔体の製造方法を提供することを追加的な課題とする。
また、本発明は、ＣＯ2吸着剤を用いたＣＯ2吸脱着方法を提供することを追加的な課題とする。
The present invention has been made in view of the present situation, and provides a zirconium hydroxide mesoporous material useful as a CO 2 adsorbent having a high CO 2 adsorption amount substantially equal to or higher than that of the
Another object of the present invention is to provide a CO 2 adsorbent comprising a zirconium hydroxide mesoporous material having a predetermined CO 2 adsorption amount.
Moreover, this invention makes it an additional subject to provide the manufacturing method of the zirconium hydroxide mesoporous body which is simpler than the conventional method and can be manufactured without heating.
The present invention is directed to additional object is to provide a CO 2 adsorption-desorption method using the CO 2 adsorbent.
本発明者は、前記課題のもと各種の固体吸着剤について検討し、その過程で、（ア）水酸化ジルコニウムは、ゼオライトと同様に優れた耐久性を有し、同時に不燃性で毒性や腐食性も少ない、環境負荷の低い材料であること、（イ）水酸化ジルコニウムはゼオライトに比べて真密度が高く重量の大きい材料であるため、排ガス流通による固体吸着剤の流動化を低減できる可能性が考えられたことから、水酸化ジルコニウム多孔体に着目した。 The present inventor examined various solid adsorbents under the above-mentioned problems. In the process, (a) zirconium hydroxide has excellent durability similar to zeolite, and at the same time is nonflammable, toxic and corrosive. (I) Zirconium hydroxide is a material with higher true density and higher weight than zeolite, so it can reduce fluidization of the solid adsorbent due to exhaust gas circulation. Therefore, attention was paid to the zirconium hydroxide porous body.
水酸化ジルコニウム多孔体は、酸化ジルコニウム製造用の出発素材、触媒や触媒担体用材料としてではあるが、比表面積が高いものも知られている（特許文献３、４参照）。
例えば、特許文献３には、水酸化ナトリウムとジルコニウム原料を混合した出発溶液に硫酸塩を添加して、溶液温度を低温に保持し(−2℃)その後水熱処理を施すことで高比表面積水酸化ジルコニウムの合成に成功したことが記載されている。
また、特許文献４には、アンモニアとジルコニウム原料を混合した出発溶液を70℃以上で8時間以上熟成することで300m2/g以上の比表面積を有する水酸化ジルコニウムを合成したことが記載されている。
A zirconium hydroxide porous body is known as a starting material for production of zirconium oxide, a catalyst and a catalyst carrier material, but has a high specific surface area (see
For example, in
Patent Document 4 describes that zirconium hydroxide having a specific surface area of 300 m 2 / g or more was synthesized by aging a starting solution in which ammonia and a zirconium raw material were mixed at 70 ° C. or more for 8 hours or more. Yes.
しかしながら、これらの水酸化ジルコニウム多孔体は、ＣＯ2吸着性能について全く検討されておらず、ＣＯ2吸着性能に適したメソ多孔構造を有しているとはいえないし、また、それらの合成方法は、比表面積が大きな水酸化ジルコニウムを得るために、高温でかつ長時間の水熱処理や長時間の熟成操作を必要とするもので、製造工程の面でも必ずしも望ましいものではなかった。 However, these zirconium hydroxide porous body has not been studied at all for the CO 2 adsorption performance, to not be to have a mesoporous structure suitable for CO 2 adsorption performance, also methods for their synthesis In order to obtain zirconium hydroxide having a large specific surface area, a high-temperature and long-time hydrothermal treatment and a long-time aging operation are required, which is not necessarily desirable in terms of the production process.
本発明者は、水酸化ジルコニウム多孔体に着目し、その可能性についてさらに検討を進める過程で、水酸化ジルコニウム多孔体はその表面特性によってＣＯ2吸着能を有することを知見したが、一方で、高いＣＯ2吸着性能を達成するためには、ＣＯ2吸着性能に適したメソ多孔構造を有するものの合成が必要であることも認識した。 The present inventor noticed that the zirconium hydroxide porous body has a CO 2 adsorption ability due to its surface characteristics in the process of further studying the possibility by paying attention to the zirconium hydroxide porous body, It has also been recognized that in order to achieve high CO 2 adsorption performance, it is necessary to synthesize one having a mesoporous structure suitable for CO 2 adsorption performance.
本発明者は、高いＣＯ2吸着性能を有する水酸化ジルコニウムメソ多孔体を得るべく、その製造方法や製造条件等について、さらに検討を加えた結果、特定の条件下で、ジルコニウム原料である金属塩の加水分解・重縮合反応を行うことにより、室温か又は同程度の低温度下、短時間で、高いＣＯ2吸着性能を有する水酸化ジルコニウムメソ多孔体を製造しうることを知見した。 The present inventor has further studied the production method and production conditions in order to obtain a zirconium hydroxide mesoporous material having high CO 2 adsorption performance, and as a result, the metal salt which is a zirconium raw material under specific conditions. It has been found that a zirconium hydroxide mesoporous material having high CO 2 adsorption performance can be produced in a short time at room temperature or at a low temperature of the same degree by performing the hydrolysis / polycondensation reaction.
本発明は上述のような検討結果や知見に基づいて完成に至ったものであり、本発明によれば、以下の発明が提供される。
（１）水が共存しない環境下において、平衡圧力10kPa、100kPa、1000kPa、3000kPaにおけるそれぞれの平衡ＣＯ2吸着量Ｖcc(STP)/mLが次の範囲であることを特徴とする水酸化ジルコニウムメソ多孔体。
20cc(STP)/mL ≦ 10kPaの時のＣＯ2吸着量Ｖ ≦ 40cc(STP)/mL
40cc(STP)/mL ≦ 100kPaの時のＣＯ2吸着量Ｖ ≦ 60cc(STP)/mL
80cc(STP)/mL ≦ 1000kPaの時のＣＯ2吸着量Ｖ ≦ 100cc(STP)/mL
110cc(STP)/mL ≦ 3000kPaの時のＣＯ2吸着量Ｖ ≦ 140cc(STP)/mL
（２）水共存下において、平衡圧力10kPa、100kPa、1000kPa、3000kPaにおけるそれぞれの平衡ＣＯ2吸着量Ｖcc(STP)/mLが次の範囲である(１)に記載の水酸化ジルコニウムメソ多孔体。
5cc(STP)/mL ≦ 10kPaの時のＣＯ2吸着量Ｖ ≦ 40cc(STP)/mL
15cc(STP)/mL ≦ 100kPaの時のＣＯ2吸着量Ｖ ≦ 50cc(STP)/mL
25cc(STP)/mL ≦ 1000kPaの時のＣＯ2吸着量Ｖ ≦ 60cc(STP)/mL
35cc(STP)/mL ≦ 3000kPaの時のＣＯ2吸着量Ｖ ≦ 80cc(STP)/mL
（３）(１)又は(２)に記載の水酸化ジルコニウムメソ多孔体からなることを特徴とする二酸化炭素吸着剤。
（４）(１)又は(２)に記載の水酸化ジルコニウムメソ多孔体の製造方法であって、室温下又は室温から60℃の温度下、pH13.0以上の水酸化ナトリウム水溶液にジルコニウム原料を添加して反応させた後、液相中に生じた固体沈殿物を液相から分離することを特徴とする水酸化ジルコニウムメソ多孔体の製造方法。
（５）分離後の固体沈殿物を、60℃以下で乾燥することを特徴とする(４)に記載の水酸化ジルコニウムメソ多孔体の製造方法。
（６）前記ジルコニウム原料が、硝酸ジルコニル、塩化ジルコニウム及び炭酸ジルコニウムアンモニウムから選択される１種又は２種以上であることを特徴とする(４)又は(５)に記載の水酸化ジルコニウムメソ多孔体の製造方法。
（７）(３)に記載の二酸化炭素吸着剤を用い、室温下、0.1〜3000kPa下での加圧・減圧操作のみにより二酸化炭素を吸脱着させることを特徴とする二酸化炭素の吸脱着方法。
（８）水共存下において、二酸化炭素を吸脱着させることを特徴とする(７)に記載の二酸化炭素の吸脱着方法。
The present invention has been completed based on the above examination results and knowledge, and according to the present invention, the following inventions are provided.
(1) Zirconium hydroxide mesoporous, characterized in that the equilibrium CO 2 adsorption amount Vcc (STP) / mL at the equilibrium pressures of 10 kPa, 100 kPa, 1000 kPa, and 3000 kPa is in the following ranges in an environment where water does not coexist. body.
20 cc (STP) / mL ≤ CO 2 adsorption amount when 10 kPa V ≤ 40 cc (STP) / mL
40cc (STP) / mL ≦
80 cc (STP) / when the mL ≦ 1000 kPa CO 2 adsorption amount V ≦ 100cc (STP) / mL
110cc (STP) / mL ≦
(2) The zirconium hydroxide mesoporous material according to (1), wherein each equilibrium CO 2 adsorption amount Vcc (STP) / mL at equilibrium pressures of 10 kPa, 100 kPa, 1000 kPa, and 3000 kPa is in the following range in the presence of water.
5 cc (STP) / mL ≤ CO 2 adsorption amount at 10 kPa V ≤ 40 cc (STP) / mL
15 cc (STP) / mL ≤ CO 2 adsorption amount when 100 kPa V ≤ 50 cc (STP) / mL
25cc (STP) / mL ≦
35cc (STP) / mL ≤ 3000kPa CO 2 adsorption amount V ≤ 80cc (STP) / mL
(3) A carbon dioxide adsorbent comprising the mesoporous zirconium hydroxide according to (1) or (2).
(4) A method for producing a zirconium hydroxide mesoporous material according to (1) or (2), wherein a zirconium raw material is added to an aqueous sodium hydroxide solution having a pH of 13.0 or more at room temperature or at a temperature from room temperature to 60 ° C. A method for producing a zirconium hydroxide mesoporous material, comprising adding and reacting, and then separating a solid precipitate generated in the liquid phase from the liquid phase.
(5) The method for producing a zirconium hydroxide mesoporous material according to (4), wherein the separated solid precipitate is dried at 60 ° C. or lower.
(6) The zirconium hydroxide mesoporous material according to (4) or (5), wherein the zirconium raw material is one or more selected from zirconyl nitrate, zirconium chloride and ammonium zirconium carbonate Manufacturing method.
(7) A method for adsorbing and desorbing carbon dioxide, comprising using the carbon dioxide adsorbent according to (3) and adsorbing and desorbing carbon dioxide only by pressurizing and depressurizing operations at room temperature and under 0.1 to 3000 kPa.
(8) The method for adsorbing and desorbing carbon dioxide according to (7), wherein carbon dioxide is adsorbed and desorbed in the presence of water.
本発明の水酸化ジルコニウムメソ多孔体は、高いＣＯ2吸着量（単位体積当たりのＣＯ2吸着量）を有するもので、そのＣＯ2吸着量は、従来のゼオライトよりも高く、従来のアミン溶液と比べてもほぼ同等かそれ以上である。また、ＣＯ2導入圧(ＣＯ2導入圧0.1〜3000kPa)下での加圧・減圧操作のみによってＣＯ2を吸脱着可能であって、アミン溶液を用いた化学吸収法のようなＣＯ2分離の際に熱エネルギーを必要としないため、水酸化ジルコニウムメソ多孔体のＣＯ2吸着剤としての利用は、省エネルギーなＣＯ2分離・回収プロセスを可能とする。
また、本発明の水酸化ジルコニウムメソ多孔体は、水共存下においてもＣＯ2導入圧(ＣＯ2導入圧0.1〜3000kPa)下で加圧・減圧操作のみによってＣＯ2を吸脱着可能であって、ゼオライトの除湿プロセスの際に熱エネルギーを必要としないため、水酸化ジルコニウムメソ多孔体のＣＯ2吸着剤としての利用は、水共存下において省エネルギーなＣＯ2分離・回収プロセスを可能とする。
本発明の製造方法によれば、高温・長時間の水熱処理を必要とせず、室温下や60℃以下の低い温度下、短時間で約300m2/g以上の高い比表面積を有するとともに、高いＣＯ2吸着量を有する水酸化ジルコニウムメソ多孔体を製造することができる。
また、本発明の水酸化ジルコニウムメソ多孔体は、ＣＯ2導入圧1000kPaにおいて約4mmol/mLのＣＯ2吸着量を示し、ゼオライトの約1.1倍（3.7mmol/mL、実測値）であり、さらに、ＣＯ2導入圧3000kPaで約5.4mmol/mLのＣＯ2吸着量を示し、ゼオライトの約1.5倍（3.7mmol/mL、実測値）高いＣＯ2吸着量を示す。
Zirconium hydroxide mesoporous material of the present invention, those having a high CO 2 adsorption amount (CO 2 adsorption amount per unit volume), the CO 2 adsorption amount is higher than conventional zeolite, the conventional amine solution It is almost equal or better than that. Further, only by pressurizing and depressurizing operations under CO 2 introduction pressure (CO 2 introduction pressure 0.1～3000KPa) of CO 2 a possible adsorption-desorption, of CO 2 separation, such as chemical absorption method using amine solution Since no thermal energy is required, the use of zirconium hydroxide mesoporous material as a CO 2 adsorbent enables an energy-saving CO 2 separation and recovery process.
Further, the zirconium hydroxide mesoporous material of the present invention can adsorb and desorb CO 2 only by pressurization and depressurization operations under CO 2 introduction pressure (CO 2 introduction pressure 0.1 to 3000 kPa) even in the presence of water, Since heat energy is not required during the dehumidification process of zeolite, the use of zirconium hydroxide mesoporous material as a CO 2 adsorbent enables an energy-saving CO 2 separation and recovery process in the presence of water.
According to the production method of the present invention, high temperature and long time hydrothermal treatment is not required, it has a high specific surface area of about 300 m 2 / g or more in a short time at room temperature or at a low temperature of 60 ° C. or less, and high A zirconium hydroxide mesoporous material having a CO 2 adsorption amount can be produced.
The zirconium hydroxide mesoporous material of the present invention exhibits a CO 2 adsorption amount of about 4 mmol / mL at a CO 2 introduction pressure of 1000 kPa, which is about 1.1 times that of zeolite (3.7 mmol / mL, measured value). CO 2 introduction pressure 3000kPa at illustrates the CO 2 adsorption amount of about 5.4 mmol / mL, indicating a 1.5-fold of the zeolite (3.7 mmol / mL, measured value) high CO 2 adsorption amount.
さらに、本発明の水酸化ジルコニウムメソ多孔体は、10-3000kPaで加圧・減圧操作を行った場合、約3.8mmol/mLの有効ＣＯ2吸着量(3000kPaと10kPaでの平衡ＣＯ2吸着量の差)を示し、既存のゼオライト（1.5mmol/mL、実測値）よりも約2.5倍高い。また、水酸化ジルコニウムメソ多孔体は100-3000kPaで加圧・減圧操作を行った場合、約3.2mmol/mLの有効ＣＯ2吸着量(3000kPaと100kPaでの平衡ＣＯ2吸着量の差)を示し、既存のゼオライト（0.6mmol/mL、実測値）よりも約5.3倍高い。ゼオライトは500kPa以上ではＣＯ2吸着量がほとんど増加せず、500-3000kPaの加圧・減圧操作で有効な吸脱着はほとんど行えないのに対し、本発明の水酸化ジルコニウムメソ多孔体は、500kPa以上でも圧力の増加とともにＣＯ2吸着量が増加するので、500-3000kPaの加圧・減圧操作で有効な吸脱着を行うことができる。 Furthermore, the zirconium hydroxide mesoporous material of the present invention has an effective CO 2 adsorption amount of about 3.8 mmol / mL (the equilibrium CO 2 adsorption amount at 3000 kPa and 10 kPa when the pressure / decompression operation is performed at 10-3000 kPa. Difference), about 2.5 times higher than the existing zeolite (1.5 mmol / mL, measured value). The zirconium hydroxide mesoporous material shows an effective CO 2 adsorption amount of about 3.2 mmol / mL (difference in equilibrium CO 2 adsorption amount between 3000 kPa and 100 kPa) when pressurized and decompressed at 100-3000 kPa. , About 5.3 times higher than existing zeolite (0.6 mmol / mL, measured value). Zeolite does not substantially increase CO 2 adsorption at 500 kPa or more, and effective adsorption / desorption can hardly be performed by pressurizing / depressurizing operation of 500-3000 kPa, whereas zirconium hydroxide mesoporous material of the present invention is 500 kPa or more However, since the amount of CO 2 adsorption increases as the pressure increases, effective adsorption and desorption can be performed by pressurization and decompression operations of 500 to 3000 kPa.
さらに、本発明の水酸化ジルコニウムメソ多孔体は、水共存下でも、ＣＯ2導入圧1000kPa及び3000kPaにおいてそれぞれ約1.4mmol/mL以上及び1.9mmol/mL以上のＣＯ2吸着量を示す。一方で水共存下では、ゼオライトのＣＯ2吸着量は著しく低下する。 Further, zirconium hydroxide mesoporous material of the present invention, even in presence of water, indicating the CO 2 introduction pressure 1000kPa and CO 2 adsorption amount of more thereof about 1.4 mmol / mL or more and 1.9 mmol / mL in 3000 kPa. On the other hand, in the presence of water, the amount of CO 2 adsorbed on the zeolite is significantly reduced.
本発明の水酸化ジルコニウムメソ多孔体の製造方法は、室温下又は室温から60℃の温度下で、ゾル−ゲル反応を利用した方法、言い換えれば、ジルコニウム原料の加水分解・重縮合反応を利用して無機構造体を得る液相合成法によるものであり、室温下で、水酸化ナトリウム水溶液にジルコニウム原料を反応させた後、液相中に生じた固体沈殿物を分離することにより、約302m2/g以上の高い比表面積を有する水酸化ジルコニウムメソ多孔体を製造する方法と、該製造方法により得られた水酸化ジルコニウムメソ多孔体からなるＣＯ2吸着剤を提供するものである。 The method for producing a zirconium hydroxide mesoporous material of the present invention is a method using a sol-gel reaction at room temperature or a temperature from room temperature to 60 ° C., in other words, utilizing a hydrolysis / polycondensation reaction of a zirconium raw material. Thus, by reacting a zirconium raw material with an aqueous sodium hydroxide solution at room temperature and separating a solid precipitate generated in the liquid phase at room temperature, about 302 m 2 is obtained. The present invention provides a method for producing a zirconium hydroxide mesoporous material having a high specific surface area of at least 10 g / g, and a CO 2 adsorbent comprising the zirconium hydroxide mesoporous material obtained by the production method.
図１に、本発明における水酸化ジルコニウムメソ多孔体の製造プロセスを示す。
水を溶媒とした強塩基下で、ジルコニウム原料を含む無機前駆体溶液を調製後、室温で数時間の撹拌を行い、水酸化ジルコニウムナノ粒子（一次粒子）を均一核発生させる。その後、水酸化ジルコニウムナノ粒子は液相中で凝集し、約数μmの大きさを持った二次粒子として沈殿する。最終的に、遠心分離によって液相から分離した沈殿粒子を空気乾燥することで、凝集粒子間の間隙にメソ細孔が形成され、水酸化ジルコニウムメソ多孔体を得る。メソ細孔を有した水酸化ジルコニウムの表面をＣＯ2吸着サイトとして利用することができる。
FIG. 1 shows a process for producing a zirconium hydroxide mesoporous material according to the present invention.
After preparing an inorganic precursor solution containing a zirconium raw material under a strong base using water as a solvent, the mixture is stirred for several hours at room temperature to uniformly generate zirconium hydroxide nanoparticles (primary particles). Thereafter, the zirconium hydroxide nanoparticles aggregate in the liquid phase and precipitate as secondary particles having a size of about several μm. Finally, the precipitated particles separated from the liquid phase by centrifugation are air-dried, whereby mesopores are formed in the gaps between the aggregated particles, and a zirconium hydroxide mesoporous material is obtained. The surface of zirconium hydroxide having mesopores can be used as a CO 2 adsorption site.
本発明においては、上記合成プロセスにおける塩基性水溶液として、pH13.0以上の水酸化ナトリウム溶液を用い、これにジルコニウム原料を添加することにより、加熱することなく、室温下、短時間で、液相中に固体沈殿物として高比表面積及び高ＣＯ2吸着量を有する水酸化ジルコニウムメソ多孔体を得ることができる。 In the present invention, as a basic aqueous solution in the above synthesis process, a sodium hydroxide solution having a pH of 13.0 or more is used, and by adding a zirconium raw material thereto, the liquid phase is obtained at room temperature in a short time without heating. A zirconium hydroxide mesoporous material having a high specific surface area and a high CO 2 adsorption amount as a solid precipitate can be obtained.
本発明において、水酸化ナトリウム水溶液に添加するジルコニウム原料としては、硝酸ジルコニル、塩化ジルコニウム及び炭酸ジルコニウムアンモニウム等が用いられ、好ましくは、硝酸ジルコニルが用いられる。 In the present invention, as a zirconium raw material to be added to an aqueous sodium hydroxide solution, zirconyl nitrate, zirconium chloride, ammonium zirconium carbonate and the like are used, and preferably zirconyl nitrate is used.
ジルコニウム原料の添加後、室温で数時間、好ましくは24時間撹拌した後、室温下で数時間、好ましくは5分以上静置することにより、液相中に、水酸化ジルコニウムナノ粒子が凝集した固体沈殿物が得られる。得られた固体沈殿物は、遠心分離後、純水を用いて洗浄することにより、残存する水酸化ナトリウム及び硝酸成分等の副生成物を完全に除去する。
洗浄後の固体沈殿物の乾燥方法は、特に限定されないが、好ましくは、25〜60℃の範囲において、12〜24時間空気雰囲気下で乾燥させるのが好ましい。
After the addition of the zirconium raw material, after stirring for several hours at room temperature, preferably 24 hours, and then standing at room temperature for several hours, preferably 5 minutes or more, a solid in which zirconium hydroxide nanoparticles are aggregated in the liquid phase A precipitate is obtained. The obtained solid precipitate is washed with pure water after centrifugation to completely remove residual by-products such as sodium hydroxide and nitric acid components.
The method for drying the solid precipitate after washing is not particularly limited, but preferably it is dried in an air atmosphere at 25 to 60 ° C. for 12 to 24 hours.
以下、本発明を実施例に基づいて説明するが、本発明はこの実施例に限定されるものではない。 EXAMPLES Hereinafter, although this invention is demonstrated based on an Example, this invention is not limited to this Example.
（実施例１：水酸化ジルコニウムメソ多孔体の製造）
以下の手順で、水酸化ジルコニウムメソ多孔体を製造した。
純水600gに水酸化ナトリウムを添加し、室温下で10分撹拌して、pHが、12.84、13.27、13.39、及び13.49である４種類の水酸化ナトリウム水溶液を調製した。
次いで、得られた水酸化ナトリウム水溶液に、硝酸ジルコニル２水和物を3、5、7、10、15、20、25または30g添加し、室温下で24時間撹拌し、5分間室温で静置した（組成条件は表１参照）。
その結果、pHが12.84の水酸化ナトリウム水溶液を用いた場合には沈殿が起こらなかったが、それ以外の水酸化ナトリウム水溶液では、液相中に固体沈殿物が得られた。
(Example 1: Production of zirconium hydroxide mesoporous material)
A zirconium hydroxide mesoporous material was produced by the following procedure.
Sodium hydroxide was added to 600 g of pure water and stirred at room temperature for 10 minutes to prepare four types of aqueous sodium hydroxide solutions having pHs of 12.84, 13.27, 13.39, and 13.49.
Next, 3, 5, 7, 10, 15, 20, 25 or 30 g of zirconyl nitrate dihydrate was added to the obtained aqueous sodium hydroxide solution, stirred at room temperature for 24 hours, and allowed to stand at room temperature for 5 minutes. (See Table 1 for composition conditions).
As a result, precipitation did not occur when an aqueous sodium hydroxide solution having a pH of 12.84 was used, but solid precipitates were obtained in the liquid phase with other aqueous sodium hydroxide solutions.
液相中に生じた固体の沈殿物を、吸引濾過で、分離し、得られた固体沈殿物を超純水で数回洗浄し、残存している水酸化ナトリウム及び硝酸成分を完全に除去した。
洗浄後、固体沈殿物を60℃で、12時間、空気雰囲気下で乾燥させた。
なお、pHが12.84の水酸化ナトリウム水溶液を用いた場合には、濾紙による吸引濾過では粒子が細か過ぎて回収できず、遠心分離、乾燥によって粒子は回収できたが、後述のＮ２吸脱着測定によれば、回収粒子は細孔を有するものとは言えなかった。
The solid precipitate formed in the liquid phase was separated by suction filtration, and the obtained solid precipitate was washed several times with ultrapure water to completely remove the remaining sodium hydroxide and nitric acid components. .
After washing, the solid precipitate was dried at 60 ° C. for 12 hours in an air atmosphere.
In the case where the pH with sodium hydroxide solution 12.84 can not recovered too fine particles in the suction filtration through filter paper, centrifuged, the particles could be recovered by drying, N 2 adsorption-desorption measurements described below According to the results, the recovered particles could not be said to have pores.
（実施例２：乾燥後の固体沈殿物のキャラクタリゼーション）
実施例１で得られた乾燥後の固体沈殿物について、粉末Ｘ線回折(XRD)、示差熱重量分析（TG-DTA）、走査型電子顕微鏡観察（FE-SEM）、Ｎ2吸脱着測定、及びＣＯ2吸脱着測定を行った。
比較のため、市販のゼオライト13Xについてもキャラクタリゼーションを行った。
(Example 2: Characterization of solid precipitate after drying)
For the solid precipitate after drying obtained in Example 1, powder X-ray diffraction (XRD), differential thermogravimetric analysis (TG-DTA), scanning electron microscope observation (FE-SEM), N 2 adsorption / desorption measurement, And CO 2 adsorption / desorption measurement was performed.
For comparison, the
〈粉末Ｘ線回折(XRD)の結果〉
図２にpH＝13.39(RUN 10)の水酸化ナトリウム水溶液に硝酸ジルコニル２水和物を添加して得られた生成物（固体沈殿物）のXRD回折パターンを示す。結晶に由来する回折パターンは確認されず、2θ = 20-40°及び2θ = 40-70°の範囲にブロードなハローパターンを示したことから、生成物は非晶質構造をとっている。他の組成で調製した固体沈殿物においても、RUN 10と同様な非晶質由来のXRDパターンが確認された。
一方で、pH＝12.84の水酸化ナトリウム水溶液に硝酸ジルコニル２水和物を添加しても、水酸化ジルコニウムの沈殿が起こらなかったことから、今回の実験系において、水酸化ナトリウム水溶液のpHは13.27以上で調製することが望ましい。
<Powder X-ray diffraction (XRD) results>
FIG. 2 shows an XRD diffraction pattern of a product (solid precipitate) obtained by adding zirconyl nitrate dihydrate to an aqueous sodium hydroxide solution having a pH = 13.39 (RUN 10). The diffraction pattern derived from the crystal was not confirmed, and a broad halo pattern was shown in the range of 2θ = 20-40 ° and 2θ = 40-70 °, and thus the product had an amorphous structure. Also in solid precipitates prepared with other compositions, an amorphous XRD pattern similar to RUN 10 was confirmed.
On the other hand, even when zirconyl nitrate dihydrate was added to an aqueous sodium hydroxide solution having a pH = 12.84, precipitation of zirconium hydroxide did not occur. In this experimental system, the pH of the aqueous sodium hydroxide solution was 13.27. It is desirable to prepare by the above.
〈示差熱重量分析（TG-DTA）の結果〉
図３にpH＝13.39 (RUN 10)で調製した水酸化ナトリウム水溶液に硝酸ジルコニル２水和物を添加して得られた固体沈殿物の示差熱重量分析(TG-DTA)の結果を示す。室温から200℃に見られる重量減少（TG）は生成物内に吸着した水分の蒸発に由来する。200℃から800℃までに見られる重量減少は生成物表面に存在するOH基の脱離によるものである。また、430℃付近に見られるシャープなDTAピークは、水酸化ジルコニウムから酸化ジルコニウムへの構造転移を示しており、XRD及びTG-DTAの結果から、生成物は非晶質構造を有した水酸化ジルコニウムであることがわかる。他の組成で合成した生成物についても類似したTG-DTAプロファイルが確認されている。
<Results of differential thermogravimetric analysis (TG-DTA)>
FIG. 3 shows the results of differential thermogravimetric analysis (TG-DTA) of the solid precipitate obtained by adding zirconyl nitrate dihydrate to an aqueous sodium hydroxide solution prepared at pH = 13.39 (RUN 10). The weight loss (TG) seen from room temperature to 200 ° C. is due to the evaporation of moisture adsorbed in the product. The weight loss seen from 200 ° C. to 800 ° C. is due to the elimination of OH groups present on the product surface. In addition, the sharp DTA peak seen around 430 ° C shows the structural transition from zirconium hydroxide to zirconium oxide. From the results of XRD and TG-DTA, the product has a hydroxyl structure with an amorphous structure. It can be seen that it is zirconium. Similar TG-DTA profiles have been confirmed for products synthesized with other compositions.
〈走査型電子顕微鏡観察（FE-SEM）の結果〉
図４にpH＝13.39 (Run 10)で調製した水酸化ナトリウム水溶液に硝酸ジルコニル２水和物を添加して得られた固体沈殿物のFE-SEM観察結果を示す。
FE-SEM観察の結果、マイクロメートルオーダーの２次粒子が得られており、粒子表面を拡大観察すると、水酸化ジルコニウムナノ粒子が凝集構造をとっていることが分かった。
<Results of scanning electron microscope observation (FE-SEM)>
FIG. 4 shows the results of FE-SEM observation of a solid precipitate obtained by adding zirconyl nitrate dihydrate to an aqueous sodium hydroxide solution prepared at pH = 13.39 (Run 10).
As a result of FE-SEM observation, secondary particles of micrometer order were obtained, and it was found that the zirconium hydroxide nanoparticles had an agglomerated structure when the particle surface was magnified.
〈Ｎ2吸脱着測定結果〉
図５〜９にRUN 1-17の77KにおけるＮ2吸脱着等温線を示す。測定前に前処理を行い、水酸化ジルコニウムメソ多孔体(RUN 1〜17)は24時間、室温で真空排気を行っている。RUN 1〜17で得られた生成物は吸脱着等温線にヒステレシスを示すことから水酸化ジルコニウムナノ粒子の凝集構造体にメソ細孔が形成されていることが示唆された。また、硝酸ジルコニル２水和物の添加量を増加させると、ヒステレシスの形も変化したことから、凝集構造に変化が起きていることを示唆する。
<N 2 adsorption / desorption measurement results>
5-9 show N 2 adsorption / desorption isotherms at 77K of RUN 1-17. Pretreatment was performed before measurement, and the zirconium hydroxide mesoporous material (
〈比表面積、細孔容積、平均一次粒子径の算出〉
Ｎ2吸脱着測定結果からBrunauer-Emmett-Teller(BET)法及びGurvich法で算出したセリアメソ多孔体の比表面積及び細孔容積を表２に示す。また、BET比表面積から見積もった水酸化ジルコニウムナノ粒子の平均一次粒子径を表２に示す（なお、平均一次粒子径の見積もりは、F.Rouquerol,J.Rouuquerol,K.Sing著「Adsorpition by Powders and Porous Solids, Principles,Methodology and Applications」P6-8に記載の式(1,1)に基づく）。
<Calculation of specific surface area, pore volume, average primary particle size>
Table 2 shows the specific surface area and pore volume of the ceria mesoporous material calculated by the Brunauer-Emmett-Teller (BET) method and the Gurvich method from the N 2 adsorption / desorption measurement results. The average primary particle diameter of zirconium hydroxide nanoparticles estimated from the BET specific surface area is shown in Table 2 (the average primary particle diameter is estimated by "Adsorpition by Powders" by F. Rouquerol, J. Rouuquerol, K. Sing). and Porous Solids, Principles, Methodology and Applications ”based on formula (1,1) described on page 6-8).
pH＝13.27〜13.49で得られた水酸化ジルコニウムメソ多孔体は302〜396m2/gの比表面積及び0.168〜0.275cm3/gの細孔容積を示し、水酸化ジルコニウムメソ多孔体RUN 10が最も高い比表面積396m2/gを示し、RUN 13が最も大きい細孔容積0.275cm3/gを示した。
The zirconium hydroxide mesoporous material obtained at pH = 13.27 to 13.49 shows a specific surface area of 302 to 396 m 2 / g and a pore volume of 0.168 to 0.275 cm 3 / g, and the zirconium hydroxide
以上、XRD、TG-DTA、SEM、及びＮ2吸脱着測定の結果、pH≧13.0で調整した水酸化ナトリウム水溶液にジルコニウム原料である硝酸ジルコニル２水和物を投入することで、直径約4.9〜6.2nmの多面体形状の水酸化ジルコニウムナノ粒子が生成し、これらが凝集して三次元構造を形成していることがわかった。Ｎ2吸脱着測定の結果、水酸化ジルコニウムナノ粒子の凝集構造を形成させることで、約300〜400m2/gの高比表面積及び0.17〜0.28cm3/gの細孔容積を有する水酸化ジルコニウムメソ多孔体を短時間で合成できることがわかった。 As described above, as a result of XRD, TG-DTA, SEM, and N 2 adsorption / desorption measurement, by introducing zirconyl nitrate dihydrate as a zirconium raw material into an aqueous sodium hydroxide solution adjusted at pH ≧ 13.0, a diameter of about 4.9˜ It was found that 6.2 nm polyhedral zirconium hydroxide nanoparticles were formed and aggregated to form a three-dimensional structure. As a result of N 2 adsorption / desorption measurement, zirconium hydroxide having a high specific surface area of about 300 to 400 m 2 / g and a pore volume of 0.17 to 0.28 cm 3 / g by forming an aggregated structure of zirconium hydroxide nanoparticles. It was found that mesoporous materials can be synthesized in a short time.
〈ＣＯ２吸脱着測定の結果〉
図１０〜１３に水酸化ジルコニウムメソ多孔体、市販のジルコニア、及び市販のゼオライト13Xの298KにおけるＣＯ2吸脱着等温線を示す。
ここでは水酸化ジルコニウムメソ多孔体(RUN 10,11,12,13)を選択し、ＣＯ2吸着能について評価した。
<CO 2 a result of the adsorption-desorption measurement>
FIGS. 10 to 13 show CO 2 adsorption and desorption isotherms at 298 K of zirconium hydroxide mesoporous material, commercially available zirconia, and commercially
Here, zirconium hydroxide mesoporous materials (
図１０〜１３に示すように、水酸化ジルコニウムメソ多孔体は室温のＣＯ2導入圧(ＣＯ2導入圧10〜3000kPa)下で加圧・減圧操作のみによってＣＯ2を吸脱着可能であることがわかった。 As shown in FIGS. 10 to 13, the zirconium hydroxide mesoporous material can adsorb and desorb CO 2 only by pressurization and depressurization operations under room temperature CO 2 introduction pressure (CO 2 introduction pressure 10 to 3000 kPa). all right.
特筆すべきことは、1000-3000kPaの圧力範囲において水酸化ジルコニウムメソ多孔体は市販のジルコニアやゼオライト13Xよりも高いＣＯ2吸着量を示すことである。
図１０において、例えばRUN 10は、ＣＯ2導入圧3000kPaでゼオライト13Xは約83cm3/mL(換算して3.7mmol/mL)、ジルコニアは約4cm3/mL(換算して0.2mmol/mL)のＣＯ2吸着量を示した。これらを比較すると、水酸化ジルコニウムメソ多孔体RUN 10は132cm3/mL(換算して5.9mmol/mL)を示すことから、ゼオライト13Xの約1.6倍、ジルコニアの約30倍高いＣＯ2吸着量を有することがわかった。
It should be noted that the zirconium hydroxide mesoporous material exhibits higher CO 2 adsorption than commercial zirconia and
In FIG. 10, for example,
上記［００４１］と同様に、図１１〜１３において、RUN 11,12,13は1000-3000kPaの圧力範囲において水酸化ジルコニウムメソ多孔体は市販のジルコニアやゼオライト13Xよりも高いＣＯ2吸着量を示す。
As in the above [0041], in FIGS. 11 to 13,
さらに重要なことは、圧力変動によるＣＯ2回収を実施するために、平衡圧力差におけるＣＯ2吸着量を評価する必要がある。10-3000kPaで加圧・減圧操作を行った場合(3000kPaと10kPaでの平衡ＣＯ2吸着量の差)、水酸化ジルコニウムメソ多孔体RUN 10は約94cm3/mL (換算して4.2mmol/mL)の有効ＣＯ2吸着量を示し、既存のゼオライト33cm3/mL（1.5mmol/mL、実測値）よりも約2.8倍高い。100-3000kPaで加圧・減圧操作を行った場合(3000kPaと100kPaでの平衡ＣＯ2吸着量の差)、水酸化ジルコニウムメソ多孔体RUN 10は約76cm3/mL(換算して3.4mmol/mL)の有効ＣＯ2吸着量を示し、既存のゼオライト14cm3/mL（換算して0.6mmol/mL、実測値）よりも約5.4倍高い。ゼオライトは500kPa以上ではＣＯ2吸着量がほとんど増加せず、500-3000kPaの加圧・減圧操作で有効な吸脱着はほとんど行えないが、本発明の水酸化ジルコニウムメソ多孔体は、500kPa以上でも圧力の増加とともにＣＯ2吸着量が増加するので、500-3000kPaの加圧・減圧操作で有効な吸脱着を行うことができる。
More importantly, it is necessary to evaluate the CO 2 adsorption amount at the equilibrium pressure difference in order to perform CO 2 capture by pressure fluctuation. When pressurization / decompression operation is performed at 10-3000 kPa (difference in equilibrium CO 2 adsorption between 3000 kPa and 10 kPa), the zirconium hydroxide
上記［００４３］と同様、10-3000kPa及び100-3000kPaで加圧・減圧操作を行った場合、水酸化ジルコニウムメソ多孔体RUN 11,12,13は既存のゼオライトよりも高い平衡圧力差におけるＣＯ2吸着量を示す。
なお、RUN 1〜9,14〜17についてはＣＯ2吸着量を確かめていないが、RUN 10〜13と同様の比表面積を有するとともに、RUN 10〜13と同様にＮ2吸脱着等温線においてヒステリシスが見られることから、RUN 10〜13と同様のＣＯ2吸着性能を有するものと考えられる。
As in the above [0043], when pressurization and depressurization operations are performed at 10-3000 kPa and 100-3000 kPa, the zirconium hydroxide
In addition, CO 2 adsorption amount is not confirmed for
図１４および１５は、水酸化ジルコニウムメソ多孔体(RUN 10及び13) 及びゼオライト13Xにあらかじめ水を吸着させ、前処理せずに、ＣＯ2吸脱着測定を行った結果である。ここでは水酸化ジルコニウムメソ多孔体(RUN 10及び13)及びゼオライト13Xの水吸着量をそれぞれ、約23wt%及び19-26wt%と調整して、測定を行った。
FIGS. 14 and 15 show the results of CO 2 adsorption / desorption measurement in which zirconium hydroxide mesoporous materials (
水酸化ジルコニウムメソ多孔体は多量の水分共存下において、ＣＯ2吸着量の低下は見られるものの、100-3000kPaの圧力範囲でＣＯ2吸脱着性能を保持していた。このとき、水酸化ジルコニウムメソ多孔体はＣＯ2導入圧100kPaで約22cm3/mL(換算して1mmol/mL以上、ＣＯ2導入圧1000kPaで約35cm3/mL(換算して1.4mmol/mL)以上、ＣＯ2導入圧3000kPaで約43cm3/mL(換算して1.9mmol/mL)以上のＣＯ2吸着量を示した。一方で、ゼオライト13Xは水の先行吸着によってＣＯ2の吸着が阻害され、ＣＯ2の吸着性能は著しく低下し、10-3000kPaの圧力範囲においてＣＯ2吸着量は、ほぼ0に近い値をとった。
The zirconium hydroxide mesoporous material maintained CO 2 adsorption / desorption performance in the pressure range of 100 to 3000 kPa, although a decrease in the CO 2 adsorption amount was observed in the presence of a large amount of moisture. At this time, the zirconium hydroxide mesoporous material is about 22 cm 3 / mL at a CO 2 introduction pressure of 100 kPa (converted to 1 mmol / mL or more, about 35 cm 3 / mL at a CO 2 introduction pressure of 1000 kPa (converted to 1.4 mmol / mL). As described above, the CO 2 adsorption amount was about 43 cm 3 / mL (converted to 1.9 mmol / mL) or more at a CO 2 introduction pressure of 3000 kPa.On the other hand,
Claims (8)
20cc(STP)/mL ≦ 10kPaの時のＣＯ2吸着量Ｖ ≦ 40cc(STP)/mL
40cc(STP)/mL ≦ 100kPaの時のＣＯ2吸着量Ｖ ≦ 60cc(STP)/mL
80cc(STP)/mL ≦ 1000kPaの時のＣＯ2吸着量Ｖ ≦ 100cc(STP)/mL
110cc(STP)/mL ≦ 3000kPaの時のＣＯ2吸着量Ｖ ≦ 140cc(STP)/mL A zirconium hydroxide mesoporous material characterized in that the equilibrium CO 2 adsorption amount Vcc (STP) / mL at equilibrium pressures of 10 kPa, 100 kPa, 1000 kPa, and 3000 kPa is in the following ranges in an environment where water does not coexist.
20 cc (STP) / mL ≤ CO 2 adsorption amount when 10 kPa V ≤ 40 cc (STP) / mL
40cc (STP) / mL ≦ CO 2 adsorption amount V ≦ 60 cc when the 100kPa (STP) / mL
80 cc (STP) / when the mL ≦ 1000 kPa CO 2 adsorption amount V ≦ 100cc (STP) / mL
110cc (STP) / mL ≦ CO 2 adsorption amount V ≦ 140 cc when the 3000kPa (STP) / mL
5cc(STP)/mL ≦ 10kPaの時のＣＯ2吸着量Ｖ ≦ 40cc(STP)/mL
15cc(STP)/mL ≦ 100kPaの時のＣＯ2吸着量Ｖ ≦ 50cc(STP)/mL
25cc(STP)/mL ≦ 1000kPaの時のＣＯ2吸着量Ｖ ≦ 60cc(STP)/mL
35cc(STP)/mL ≦ 3000kPaの時のＣＯ2吸着量Ｖ ≦ 80cc(STP)/mL 2. The zirconium hydroxide mesoporous material according to claim 1, wherein each of the equilibrium CO 2 adsorption amounts Vcc (STP) / mL at the equilibrium pressures of 10 kPa, 100 kPa, 1000 kPa, and 3000 kPa is in the following range in the presence of water.
5 cc (STP) / mL ≤ CO 2 adsorption amount at 10 kPa V ≤ 40 cc (STP) / mL
15 cc (STP) / mL ≤ CO 2 adsorption amount when 100 kPa V ≤ 50 cc (STP) / mL
25cc (STP) / mL ≦ CO 2 adsorption amount V ≦ 60 cc when the 1000kPa (STP) / mL
35cc (STP) / mL ≤ 3000kPa CO 2 adsorption amount V ≤ 80cc (STP) / mL
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7162716B1 (en) | 2021-11-01 | 2022-10-28 | 第一稀元素化学工業株式会社 | zirconium hydroxide powder |
| JP7203180B1 (en) | 2021-11-01 | 2023-01-12 | 第一稀元素化学工業株式会社 | Zirconium hydroxide powder and method for producing zirconium hydroxide powder |
| CN116550276A (en) * | 2023-06-05 | 2023-08-08 | 太原科技大学 | Nano porous zirconia adsorbent and preparation method thereof |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU865381A1 (en) * | 1980-01-29 | 1981-09-23 | Ленинградский Институт Авиационного Приборостроения | Sorbent producing method |
| JP2004323257A (en) * | 2003-04-22 | 2004-11-18 | Nippon Denko Kk | High-purity zirconium hydroxide with high specific surface area, zirconium oxide and production method therefor, and molded product |
| JP2008031023A (en) * | 2006-07-28 | 2008-02-14 | Daiichi Kigensokagaku Kogyo Co Ltd | Zirconia sol and method for producing the same |
| WO2008129968A1 (en) * | 2007-04-13 | 2008-10-30 | National Institute Of Advanced Industrial Science And Technology | Carbon dioxide adsorbent capable of adsorption/desorption in dependence on pressure of atmospheric pressure or higher |
| JP2009013029A (en) * | 2007-07-06 | 2009-01-22 | Hitachi Maxell Ltd | Zirconium oxide hydrate particles and method for producing the same |
| JP2009525250A (en) * | 2006-02-03 | 2009-07-09 | マグネシウム エレクトロン リミテッド | Zirconium hydroxide |
| JP2012504095A (en) * | 2008-09-30 | 2012-02-16 | サン−ゴベン・セントル・ドゥ・レシェルシェ・エ・デチュード・ユーロペアン | Method for producing a derivative, hydrate or oxide of zirconium |
| JP2013014511A (en) * | 2004-02-06 | 2013-01-24 | Millennium Inorganic Chemicals Inc | Nano-structured zirconia particle with high thermal stability |
-
2015
- 2015-08-21 JP JP2015164223A patent/JP6663146B2/en active Active
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU865381A1 (en) * | 1980-01-29 | 1981-09-23 | Ленинградский Институт Авиационного Приборостроения | Sorbent producing method |
| JP2004323257A (en) * | 2003-04-22 | 2004-11-18 | Nippon Denko Kk | High-purity zirconium hydroxide with high specific surface area, zirconium oxide and production method therefor, and molded product |
| JP2013014511A (en) * | 2004-02-06 | 2013-01-24 | Millennium Inorganic Chemicals Inc | Nano-structured zirconia particle with high thermal stability |
| JP2009525250A (en) * | 2006-02-03 | 2009-07-09 | マグネシウム エレクトロン リミテッド | Zirconium hydroxide |
| JP2008031023A (en) * | 2006-07-28 | 2008-02-14 | Daiichi Kigensokagaku Kogyo Co Ltd | Zirconia sol and method for producing the same |
| WO2008129968A1 (en) * | 2007-04-13 | 2008-10-30 | National Institute Of Advanced Industrial Science And Technology | Carbon dioxide adsorbent capable of adsorption/desorption in dependence on pressure of atmospheric pressure or higher |
| JP2009013029A (en) * | 2007-07-06 | 2009-01-22 | Hitachi Maxell Ltd | Zirconium oxide hydrate particles and method for producing the same |
| JP2012504095A (en) * | 2008-09-30 | 2012-02-16 | サン−ゴベン・セントル・ドゥ・レシェルシェ・エ・デチュード・ユーロペアン | Method for producing a derivative, hydrate or oxide of zirconium |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7162716B1 (en) | 2021-11-01 | 2022-10-28 | 第一稀元素化学工業株式会社 | zirconium hydroxide powder |
| JP7203180B1 (en) | 2021-11-01 | 2023-01-12 | 第一稀元素化学工業株式会社 | Zirconium hydroxide powder and method for producing zirconium hydroxide powder |
| JP2023067405A (en) * | 2021-11-01 | 2023-05-16 | 第一稀元素化学工業株式会社 | Zirconium hydroxide powder and manufacturing method of zirconium hydroxide powder |
| JP2023067461A (en) * | 2021-11-01 | 2023-05-16 | 第一稀元素化学工業株式会社 | zirconium hydroxide powder |
| CN116550276A (en) * | 2023-06-05 | 2023-08-08 | 太原科技大学 | Nano porous zirconia adsorbent and preparation method thereof |
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