JPH03290304A - Generation of oxygen gas - Google Patents
Generation of oxygen gasInfo
- Publication number
- JPH03290304A JPH03290304A JP9157390A JP9157390A JPH03290304A JP H03290304 A JPH03290304 A JP H03290304A JP 9157390 A JP9157390 A JP 9157390A JP 9157390 A JP9157390 A JP 9157390A JP H03290304 A JPH03290304 A JP H03290304A
- Authority
- JP
- Japan
- Prior art keywords
- percarbonate
- earth metal
- alkaline earth
- water
- oxygen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 title claims description 3
- 229910001882 dioxygen Inorganic materials 0.000 title claims description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 28
- -1 alkaline earth metal salt Chemical class 0.000 claims abstract description 24
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 23
- 239000002798 polar solvent Substances 0.000 claims abstract description 13
- 239000003054 catalyst Substances 0.000 claims abstract description 12
- 238000000354 decomposition reaction Methods 0.000 claims abstract description 11
- 238000003756 stirring Methods 0.000 claims abstract description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 25
- 239000001301 oxygen Substances 0.000 claims description 25
- 229910052760 oxygen Inorganic materials 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 15
- 230000001737 promoting effect Effects 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 abstract description 19
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 abstract description 19
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 abstract description 5
- 229940045872 sodium percarbonate Drugs 0.000 abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 4
- WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical compound [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 abstract description 3
- 229910001626 barium chloride Inorganic materials 0.000 abstract description 3
- 239000011369 resultant mixture Substances 0.000 abstract 1
- 238000002474 experimental method Methods 0.000 description 16
- 230000007935 neutral effect Effects 0.000 description 16
- 239000000243 solution Substances 0.000 description 12
- 239000002245 particle Substances 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 239000003595 mist Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000011734 sodium Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 102000016938 Catalase Human genes 0.000 description 1
- 108010053835 Catalase Proteins 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- 102000003992 Peroxidases Human genes 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 1
- BHDAXLOEFWJKTL-UHFFFAOYSA-L dipotassium;carboxylatooxy carbonate Chemical compound [K+].[K+].[O-]C(=O)OOC([O-])=O BHDAXLOEFWJKTL-UHFFFAOYSA-L 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- YAGKRVSRTSUGEY-UHFFFAOYSA-N ferricyanide Chemical class [Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] YAGKRVSRTSUGEY-UHFFFAOYSA-N 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 108040007629 peroxidase activity proteins Proteins 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229910001631 strontium chloride Inorganic materials 0.000 description 1
- AHBGXTDRMVNFER-UHFFFAOYSA-L strontium dichloride Chemical compound [Cl-].[Cl-].[Sr+2] AHBGXTDRMVNFER-UHFFFAOYSA-L 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000009469 supplementation Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
Landscapes
- Oxygen, Ozone, And Oxides In General (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、火災、酸素欠乏、有毒ガス発生等の事故や、
病気による呼吸困難時の緊急医療用、あるいはスポーツ
前後、煙草や酒の飲み過ぎ時、仕事、勉強、本運転時等
における健康増進のための酸素補給用として用いられる
酸素ガス発生方法に関するものである。[Detailed Description of the Invention] [Industrial Application Fields] The present invention is useful for preventing accidents such as fire, oxygen deficiency, generation of toxic gas, etc.
This relates to a method for generating oxygen gas that can be used for emergency medical treatment when breathing is difficult due to illness, or for oxygen supplementation to improve health before and after sports, when smoking or drinking too much alcohol, when working, studying, driving, etc. .
[従来技術及び発明が解決しようとする課題]最近、過
炭酸塩の一つである過炭酸ナトリウム(Na2Co3・
3/2H2f)□)と、二酸化マンガン(MnO’z)
等の過酸化水素分解促進触媒の懸濁液あるいは水溶液と
を接触させることによって酸素を発生させる方法を用い
た酸素発生装置が、手軽に利用でき、安全、確実、安価
な手法として着目され、数多くの特許出願がなされてい
る。[Prior art and problems to be solved by the invention] Recently, sodium percarbonate (Na2Co3.
3/2H2f)□) and manganese dioxide (MnO'z)
Oxygen generators that generate oxygen by contacting suspensions or aqueous solutions of hydrogen peroxide decomposition promoting catalysts, such as A patent application has been filed.
しかし、過炭酸ナトリウムはアルカリ性であり、このア
ルカリ水溶液が酸素発生時にミストとなって空中に飛び
出すため、酸素吸入者が同時にこのミストを吸引すれば
有害であり、また酸素発生終了後のアルカリ水溶液の後
処理も問題となる。However, sodium percarbonate is alkaline, and when oxygen is generated, this alkaline aqueous solution turns into a mist and flies into the air, so if a person inhaling oxygen at the same time inhales this mist, it is harmful. Post-processing is also an issue.
そこでアルカリ水溶液のミストの害を防ぐため、反応に
よって発生した酸素をフィルターを通すことによってミ
ストを除去する手法が特開昭62−27307号公報に
示されているが、ミストを完全に除去することは極めて
困難であるし、装置の構造自体が複雑になるという欠点
もある。また、アルカリ水溶液の後処理の問題について
も、前記公開公報において、吸水性高分子化合物によっ
て装置内のアルカリ水溶液をゲル状に固めたうえで、こ
れを廃棄する手法が提示されているが、これにしても、
完全にアルカリ水溶液を吸水し、液が漏れないようにす
ることは事実上困難である。In order to prevent the mist from the alkaline aqueous solution from causing harm, Japanese Patent Laid-Open No. 62-27307 discloses a method of removing the mist by passing the oxygen generated by the reaction through a filter, but it is difficult to completely remove the mist. is extremely difficult, and also has the disadvantage that the structure of the device itself becomes complicated. Regarding the issue of post-treatment of alkaline aqueous solutions, the above-mentioned publication proposes a method in which the alkaline aqueous solution in the device is solidified into a gel-like state using a water-absorbing polymer compound and then disposed of. even if,
It is practically difficult to completely absorb an alkaline aqueous solution and prevent the liquid from leaking.
[課題を解決する手段]
本発明の発明者等は、上記の如き実情に鑑み鋭意研究し
た結果、強極性溶媒下で過炭酸塩と水溶性アルカリ土類
金属塩とを加えると、化学反応によって不溶性アルカリ
のアルカリ土類金属炭酸塩と水溶性の中性塩、中性の過
酸化水素溶液が得られることを見出し、本発明を完成す
るに至った。[Means for Solving the Problems] The inventors of the present invention have conducted extensive research in view of the above-mentioned circumstances, and have found that when a percarbonate and a water-soluble alkaline earth metal salt are added in a strongly polar solvent, a chemical reaction occurs. It was discovered that an insoluble alkaline earth metal carbonate, a water-soluble neutral salt, and a neutral hydrogen peroxide solution could be obtained, and the present invention was completed.
そして本発明は、強極性溶媒下で過炭酸塩、水溶性アル
カリ土類金属塩、および過酸化水素分解促進触媒を用い
、撹拌装置にて撹拌して酸素を発生させることを特徴と
するものである。The present invention is characterized in that a percarbonate, a water-soluble alkaline earth metal salt, and a hydrogen peroxide decomposition promoting catalyst are used in a strong polar solvent and are stirred with a stirring device to generate oxygen. be.
本発明を実施するにあたり、強極性溶媒としては、水溶
液が一般的である。In carrying out the present invention, an aqueous solution is generally used as the strong polar solvent.
一方、過炭酸塩としては、過炭酸ナトリウム、過炭酸カ
リウム等の過炭酸アルカリ金属塩、過炭酸カルシウム等
の過炭酸アルカリ土類金属塩、過炭酸硼素等の三価金属
の過炭酸金属塩等の各種金属塩のなかから、一種あるい
は複数を選択して用いることができる。On the other hand, examples of percarbonates include alkali metal percarbonates such as sodium percarbonate and potassium percarbonate, alkaline earth metal percarbonates such as calcium percarbonate, metal percarbonates of trivalent metals such as boron percarbonate, etc. One or more of these metal salts can be selected and used.
また水溶性アルカリ土類金属塩としては、塩化カルシウ
ム、塩化マグネシウム、塩化バリウム、塩化ストロンチ
ウム等の塩酸塩、硝酸カルシウム、硝酸マグネシウム、
硝酸バリウム、硝酸ストロンチウム等の硝酸塩、硫酸マ
グネシウム等の硫酸塩等の各種水溶性金属塩のなかから
、一種あるいは複数を選択して用いることができる。In addition, water-soluble alkaline earth metal salts include hydrochlorides such as calcium chloride, magnesium chloride, barium chloride, strontium chloride, calcium nitrate, magnesium nitrate,
One or more water-soluble metal salts can be selected and used from various water-soluble metal salts such as nitrates such as barium nitrate and strontium nitrate, and sulfates such as magnesium sulfate.
そしてこれら過炭酸塩、水溶性アルカリ土類金属塩を本
発明方法に用いるにあたり、過酸化水素発生過程の反応
で生成するアルカリ土類金属炭酸塩は不溶性物質として
溶液反応系から除外する必要が有り、そうすることによ
って反応系は、水溶性中性塩が溶解した中性の過酸化水
素溶液となるのである。When using these percarbonates and water-soluble alkaline earth metal salts in the method of the present invention, it is necessary to exclude the alkaline earth metal carbonates produced in the reaction during the hydrogen peroxide generation process from the solution reaction system as insoluble substances. By doing so, the reaction system becomes a neutral hydrogen peroxide solution in which a water-soluble neutral salt is dissolved.
さらにまた、過酸化水素分解触媒としては二酸化マンガ
ン、過マンガン酸カリウム、塩化コバルト、第二銅塩、
銅酸化物、第一鉄錯体、硫化銅、フェリシアン化塩、カ
タラーゼ、パーオキシダーゼ等の通常知られた触媒のな
かから、一種あるいは複数を選択して用いることができ
る。Furthermore, as a hydrogen peroxide decomposition catalyst, manganese dioxide, potassium permanganate, cobalt chloride, cupric salt,
One or more of commonly known catalysts such as copper oxide, ferrous complex, copper sulfide, ferricyanide salt, catalase, peroxidase, etc. can be selected and used.
そして本発明方法を実施するにあたり、過炭酸塩が水溶
性アルカリ土類金属塩と反応する際、過炭酸塩粒子が強
極性溶媒に溶ける前にその表面に反応で生成した不溶の
アルカリ炭酸塩が付着して過炭酸粒子の表面を覆って不
溶化する慣れが有り、この場合には閉じ込められた粒子
内部の過炭酸塩が反応できなくなって効率良く酸素を発
生させることができないことになり、また過炭酸塩粒子
が固まりとなってそのまま不溶化してしまうことも考え
られる。そこで過炭酸塩と水溶性アルカリ土類金属塩お
よび過酸化水素分解促進触媒の強極性溶媒下での反応を
、撹拌装置を用いて撹拌しながら行えば、過炭酸塩粒子
と強極性溶媒、水溶性アルカリ土類金属塩と強極性溶媒
との溶解が強力に促進され、不溶性粒子あるいは不溶性
粒子の固まりが生成しにくくなり、反応を効率良く行わ
せ酸素発生量を増加させることができるという利点があ
る。When carrying out the method of the present invention, when the percarbonate reacts with the water-soluble alkaline earth metal salt, the insoluble alkali carbonate formed by the reaction is deposited on the surface of the percarbonate particles before they are dissolved in the strong polar solvent. There is a habit of adhering to the surface of percarbonate particles and making them insolubilized, and in this case, the percarbonate inside the trapped particles becomes unable to react and oxygen cannot be efficiently generated. It is also possible that the carbonate particles become agglomerated and become insolubilized as they are. Therefore, if the reaction of percarbonate, water-soluble alkaline earth metal salt, and hydrogen peroxide decomposition promoting catalyst in a strong polar solvent is carried out with stirring using a stirring device, the percarbonate particles, the strong polar solvent, and the water-soluble It has the advantage that the dissolution of the strong alkaline earth metal salt and the strong polar solvent is strongly promoted, making it difficult to form insoluble particles or agglomerates of insoluble particles, allowing the reaction to occur efficiently and increasing the amount of oxygen generated. be.
この本発明方法で使用する撹拌装置としては、液体中で
羽根を回転させる手法と、液体の運動エネルギーを利用
する手法のいずれのタイプを使用しても良い。前者には
、実験室で良く用いられるマグネットスターラー等のも
のが有り、後者には、ポンプによる循環、ノズルから噴
出させる方法、スタティックミキサー等がある。As the stirring device used in the method of the present invention, either a method that rotates a blade in the liquid or a method that utilizes the kinetic energy of the liquid may be used. The former includes things such as magnetic stirrers that are often used in laboratories, while the latter include circulation using pumps, jetting from nozzles, and static mixers.
因みに、本発明方法に用いる過炭酸塩および水溶性アル
カリ土類金属塩の粒子サイズはなるへく小さいものを使
用した方が溶解し易いため反応効率的に有利である。Incidentally, it is advantageous in terms of reaction efficiency if the particle size of the percarbonate and water-soluble alkaline earth metal salt used in the method of the present invention is much smaller, since it is easier to dissolve.
さらに本発明方法の実施にあたり、強極性溶媒中への試
薬の投入手順は、強極性溶媒中に過炭酸塩および水溶性
アルカリ土類金属塩を投入した後に、過酸化水素分解促
進触媒を投入する順序が好ましいが、これに限定されず
、過炭酸塩と過酸化水素分解促進触媒を投入した後、時
間をおいて水溶性アルカリ土類金属塩を投入する順序以
外であれば、どの順序であっても良い。ただし、アルカ
リ性ミストを捕集するフィルター等を用いた装置であれ
ば、過炭酸塩と過酸化水素分解促進触媒を投入した後に
、水溶性アルカリ土類金属塩を投入する順序としても良
い。Furthermore, in carrying out the method of the present invention, the procedure for introducing reagents into a strong polar solvent is to introduce a hydrogen peroxide decomposition promoting catalyst after introducing a percarbonate and a water-soluble alkaline earth metal salt into a strong polar solvent. Although the order is preferred, the order is not limited to this, and any order other than adding the percarbonate and the hydrogen peroxide decomposition promoting catalyst and then adding the water-soluble alkaline earth metal salt after a period of time is acceptable. It's okay. However, if the device uses a filter or the like to collect alkaline mist, the water-soluble alkaline earth metal salt may be added in the order after the percarbonate and hydrogen peroxide decomposition promoting catalyst are added.
[発明の作用コ
本発明方法によれば、強極性溶媒下で過炭酸塩と水溶性
アルカリ土類金属塩とを加えると、化学反応によって不
溶性のアルカリ土類金属炭酸塩と水溶性中性塩、中性の
過酸化水素溶液が得られる。[Operation of the invention] According to the method of the invention, when a percarbonate and a water-soluble alkaline earth metal salt are added in a strong polar solvent, an insoluble alkaline earth metal carbonate and a water-soluble neutral salt are formed by a chemical reaction. , a neutral hydrogen peroxide solution is obtained.
つまり例として過炭酸塩として過炭酸ナトリウム(Na
2Co3・3/2H20□)と水溶性アルカリ土類金属
塩として塩化バリウムとを反応させたときの反応式%式
%
となって反応溶液中では、不溶性のアルカリ土類金属炭
酸塩である炭酸バリウム(BaCOi )が析出して反
応溶液系から除外され、水溶性中性塩である塩化ナトリ
ウム(Naα)が溶解した中性の過酸化水素(H2O2
)の反応溶液となり、こうして生成した過酸化水素の中
性溶液に過酸化水素分解促進触媒が作用して酸素を発生
することになる。In other words, as an example of percarbonate, sodium percarbonate (Na
2Co3・3/2H20□) and barium chloride as a water-soluble alkaline earth metal salt are reacted as follows: In the reaction solution, barium carbonate, which is an insoluble alkaline earth metal carbonate, is (BaCOi ) is precipitated and excluded from the reaction solution system, and neutral hydrogen peroxide (H2O2
), and the hydrogen peroxide decomposition promoting catalyst acts on the neutral solution of hydrogen peroxide thus produced to generate oxygen.
[発明の効果]
要するに本発明方法では、過炭酸塩を用いて酸素を発生
させる場合に、反応溶液は殆ど中性になるため、酸素発
生中に生成されるミストも中性になって安全性が高く、
そのうえ酸素発生後の残液も中性であって安全性が高く
、このまま廃棄しても殆ど問題がなく、さらに必要が有
ればこの残液において不溶性のアルカリ土類金属塩は濾
過する等して残液から簡単に分離することもでき、廃棄
処分等の後処理が安全かつ容易である。[Effect of the invention] In short, in the method of the present invention, when oxygen is generated using percarbonate, the reaction solution becomes almost neutral, so the mist generated during oxygen generation also becomes neutral, making it safer. is high;
Furthermore, the residual liquid after oxygen generation is neutral and highly safe, and there is almost no problem even if it is disposed of as is.Furthermore, if necessary, insoluble alkaline earth metal salts in this residual liquid can be filtered, etc. It can be easily separated from the residual liquid, and post-treatment such as disposal is safe and easy.
しかもこの反応は撹拌されるので1反応効率も良く、発
生酸素量が充分得られる利点がある。Moreover, since this reaction is stirred, the efficiency of each reaction is good and there is an advantage that a sufficient amount of oxygen can be generated.
次に本発明の実施例を示す。Next, examples of the present invention will be shown.
口実流側]
水IQを入れた2Ω用のビーカーを用いて次のNa 1
〜3の実験を試みた。Pretext flow side] Using a 2Ω beaker containing water IQ, add the following Na 1
~3 experiments were attempted.
・実験1
前記ビーカーを、マグネットスターラーにて撹拌しなが
ら、6gのB a 022.10gのNa2CO1・3
/2H20□、3gのMnO□を同時に投入し、該溶液
のPH及び酸素発生量(−7分、以下同じ)の経時変化
を測定した。・Experiment 1 While stirring the beaker with a magnetic stirrer, 6g of B a 022.10g of Na2CO1.3
/2H20□ and 3 g of MnO□ were added at the same time, and changes over time in the pH of the solution and the amount of oxygen generated (-7 minutes, the same applies hereinafter) were measured.
・実験2
前記ビーカーを、実験1に対する比較例として撹拌を行
わない状態で、6gのB a Cl12.10gのNa
2Co、 ・3/2H202,3gのMnO2を同時に
投入し、該溶液のpH及び酸素発生量の経時変化を測定
した。・Experiment 2 As a comparative example for Experiment 1, 6 g of B a Cl 12.10 g of Na was added to the beaker without stirring.
2Co, 3/2H202, and 3g of MnO2 were added at the same time, and the pH of the solution and the amount of oxygen generated were measured over time.
・実験3
前記ビーカーを、マグネットスターラーにて撹拌しなが
ら、前記実験1に対する比較例として、水溶性アルカリ
土類金属塩を用いることな°く、LogのNa2CO1
・3/2H20□、2gのMnO□を同時に投入し、該
溶液のpH及び酸素発生量の経時変化を測定した。・Experiment 3 While stirring the beaker with a magnetic stirrer, as a comparative example to the experiment 1, the log of Na2CO1 was added without using a water-soluble alkaline earth metal salt.
- 3/2H20□ and 2g of MnO□ were added at the same time, and the pH of the solution and the amount of oxygen generated were measured over time.
[以下余白コ これら実験1.2.3の各測定結果を表1に示す。[Margin below] Table 1 shows the measurement results of Experiments 1.2.3.
表1から明らかなように、本発明が実施された実験1の
ものは、pHについては、実験2のものに比して反応当
初において明らかに中性側にシフトし、また実験3のも
のに比して終始中性側にシフトしていることが観測され
る。また酸素発生量については、実験2のものに比して
終始価れた酸素発生が認められ、また実験3のものに比
して反応当初において優れた酸素発生が認められ、本発
明が、反応溶液を中性にした状態で酸素を発生すること
に対して如何に有効であるかが立証される。As is clear from Table 1, the pH of Experiment 1 in which the present invention was carried out was clearly shifted to the neutral side at the beginning of the reaction compared to that of Experiment 2, and it was also similar to that of Experiment 3. In comparison, a shift toward the neutral side is observed throughout. In addition, regarding the amount of oxygen generated, a higher level of oxygen generation was observed from beginning to end compared to that in Experiment 2, and superior oxygen generation was observed at the beginning of the reaction compared to that of Experiment 3. It is demonstrated how effective it is in generating oxygen while keeping the solution neutral.
さらに実験4.5として、前記実験1と同様の条件下で
、実験4のものは、6gのBaQ22に変えて3gのC
aα2を、また実験5のものはLogのNa2CO3・
3/ 2H20,に変えて12gのに2Go、−3/2
H20゜を投入し、それぞれの溶液のpH及び酸素発生
量の経時変化を測定し、その結果を表2に示す。Furthermore, as experiment 4.5, under the same conditions as in experiment 1, 3 g of C was used instead of 6 g of BaQ22.
aα2, and that of Experiment 5 is Log of Na2CO3・
3/ Change to 2H20, 12g of 2Go, -3/2
20° of H was added, and the pH and oxygen generation amount of each solution were measured over time. The results are shown in Table 2.
表2からも明らかなように、実験4.5においては略中
性溶液下で円滑な酸素の発生が認められ、ここにおいて
も本発明が1反応溶液を中性にした状態で酸素を発生す
ることに対して如何に有効であるかが立証される。As is clear from Table 2, in Experiment 4.5, smooth generation of oxygen was observed in a substantially neutral solution, and here too, the present invention was able to generate oxygen while the reaction solution was made neutral. It will be demonstrated how effective it is in this regard.
Claims (1)
および過酸化水素分解促進触媒を用い、撹拌装置にて撹
拌して酸素を発生させることを特徴とする酸素ガス発生
方法。percarbonates, water-soluble alkaline earth metal salts, under strong polar solvents;
and a hydrogen peroxide decomposition promoting catalyst, and a method of generating oxygen gas by stirring with a stirring device to generate oxygen.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9157390A JPH03290304A (en) | 1990-04-06 | 1990-04-06 | Generation of oxygen gas |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9157390A JPH03290304A (en) | 1990-04-06 | 1990-04-06 | Generation of oxygen gas |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03290304A true JPH03290304A (en) | 1991-12-20 |
Family
ID=14030274
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9157390A Pending JPH03290304A (en) | 1990-04-06 | 1990-04-06 | Generation of oxygen gas |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03290304A (en) |
-
1990
- 1990-04-06 JP JP9157390A patent/JPH03290304A/en active Pending
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