JPH06107401A - Oxygen generating agent - Google Patents
Oxygen generating agentInfo
- Publication number
- JPH06107401A JPH06107401A JP5390791A JP5390791A JPH06107401A JP H06107401 A JPH06107401 A JP H06107401A JP 5390791 A JP5390791 A JP 5390791A JP 5390791 A JP5390791 A JP 5390791A JP H06107401 A JPH06107401 A JP H06107401A
- Authority
- JP
- Japan
- Prior art keywords
- oxygen
- water
- peroxide
- particles
- generating agent
- 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.)
- Granted
Links
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title claims abstract description 68
- 239000001301 oxygen Substances 0.000 title claims abstract description 68
- 229910052760 oxygen Inorganic materials 0.000 title claims abstract description 68
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 20
- 150000002978 peroxides Chemical class 0.000 claims abstract description 17
- 102000016938 Catalase Human genes 0.000 claims abstract description 13
- 108010053835 Catalase Proteins 0.000 claims abstract description 13
- 239000003094 microcapsule Substances 0.000 claims abstract description 8
- 239000000843 powder Substances 0.000 claims abstract description 4
- 239000002245 particle Substances 0.000 claims description 28
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 claims description 14
- 229940045872 sodium percarbonate Drugs 0.000 claims description 14
- 239000011248 coating agent Substances 0.000 claims description 11
- 238000000576 coating method Methods 0.000 claims description 8
- 239000004343 Calcium peroxide Substances 0.000 claims description 7
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 claims description 7
- 235000019402 calcium peroxide Nutrition 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 19
- 239000003054 catalyst Substances 0.000 abstract description 17
- 241001465754 Metazoa Species 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- 230000009931 harmful effect Effects 0.000 abstract description 3
- 239000000376 reactant Substances 0.000 abstract 2
- 238000011109 contamination Methods 0.000 abstract 1
- 238000000151 deposition Methods 0.000 abstract 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- 238000004140 cleaning Methods 0.000 description 8
- 239000002202 Polyethylene glycol Substances 0.000 description 6
- 229920001223 polyethylene glycol Polymers 0.000 description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000005192 partition Methods 0.000 description 3
- 235000014102 seafood Nutrition 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 2
- -1 bowshaw Polymers 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000004199 lung function Effects 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Chemical class 0.000 description 2
- 239000002184 metal Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- GEMCGUOJDLYZJY-UHFFFAOYSA-N carbonic acid;hydrogen peroxide;sodium Chemical compound [Na].OO.OC(O)=O GEMCGUOJDLYZJY-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229940099596 manganese sulfate Drugs 0.000 description 1
- 239000011702 manganese sulphate Substances 0.000 description 1
- 235000007079 manganese sulphate Nutrition 0.000 description 1
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012476 oxidizable substance Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000015170 shellfish Nutrition 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B23/00—Noble gases; Compounds thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Oxygen, Ozone, And Oxides In General (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、酸素発生剤の改良に関
し、酸素発生剤として過酸化物を用いるとともに、さら
に触媒としてカタラーゼまたはレオネットを用い、これ
によって酸素の発生量および発生持続時間を自在にコン
トロールできるとともに、反応液の汚濁ならびにその有
害性を取り除き、簡便で、しかも安価であり、かつ安全
で確実な酸素発生剤を得ることを目的とする。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improvement in an oxygen generating agent, which uses a peroxide as an oxygen generating agent and catalase or rheonet as a catalyst, thereby increasing the amount of oxygen generated and the duration of generation. The purpose of the present invention is to obtain a simple, inexpensive, safe, and reliable oxygen generator that can be freely controlled, removes pollution of the reaction solution and its harmfulness.
【0002】[0002]
【従来の技術】従来の酸素発生方法としては、本出願人
らが過去に開発した炭酸ソーダと過酸化水素との付加化
合物に対し、触媒の存在下で水を加える方法が一般的に
知られている。2. Description of the Related Art As a conventional oxygen generating method, a method of adding water in the presence of a catalyst to an addition compound of sodium carbonate and hydrogen peroxide developed by the present applicants is generally known. ing.
【0003】また急激な酸素の発生を抑えて長時間一定
量の酸素供給を可能とすべく、上記した炭酸ソーダと過
酸化水素との付加化合物、および触媒としての金属塩
を、濃度の異なる複数種のアラビア糊により固化し、こ
れらの混合物に水を加えて反応させるようにして救急時
の使用に供することができるようにした酸素発生方法に
ついてもすでに特公昭60−44242号(特許第13
21792号)として公にした。Further, in order to suppress abrupt generation of oxygen and enable a constant amount of oxygen to be supplied for a long time, the above-mentioned addition compound of sodium carbonate and hydrogen peroxide, and a metal salt as a catalyst are mixed in a plurality of different concentrations. Regarding the oxygen generation method, which is solidified by a kind of arabic paste and made to react by adding water to these mixtures, which can be used for emergency, it is already disclosed in Japanese Examined Patent Publication No. 60-44242.
No. 21792).
【0004】[0004]
【発明が解決しようとする課題】上記した従来法による
場合には、安価でしかも確実な酸素供給を可能とするた
めに画期的な評価を売ることができた。 しかし酸素の
継続的な発生持続時間の面においては、たとえ上記した
特許第1321792号の発明による場合でも、平均的
に20〜30分程度であるために、急病人に対する応急
手当等の救急用としては一応満足できるものの、少なく
とも2時間以上の連続した酸素の供給が要求される低肺
機能患者の酸素吸入や、魚介類の運搬、あるいは1週間
から1ケ月間単位での連続した酸素供給が要求される植
物の育成用等の酸素発生手段としては、供給時間があま
りにも短すぎるために実用化することができない。In the case of the above-mentioned conventional method, it was possible to sell an epoch-making evaluation in order to enable reliable and reliable oxygen supply. However, in terms of continuous generation time of oxygen, even in the case of the invention of Japanese Patent No. 1321792 mentioned above, since it is about 20 to 30 minutes on average, it is used for emergency such as first aid for suddenly sick people. Although it is satisfactory for the time being, oxygen inhalation of patients with low lung function, which requires continuous oxygen supply for at least 2 hours, transportation of seafood, or continuous oxygen supply for one week to one month is required. As an oxygen generating means for growing plants, the supply time is too short to be put to practical use.
【0005】また過炭酸ソーダと触媒とを混合すると、
互いに反応するために、常に両者を別々に分包する必要
があり、使用時の不便さがあるばかりでなく、量産コス
トの面においても高価となるために実用性にかけるとこ
ろがある。When sodium percarbonate and a catalyst are mixed,
In order to react with each other, it is necessary to always package the both separately, which is not only inconvenient at the time of use but also expensive in terms of mass-production cost, which is not practical.
【0006】さらに触媒として二酸化マンガンや、硫酸
マンガンなどの金属塩を用いるために、反応後の廃液に
汚濁があり、しかもこの汚濁液は魚介類を死滅させ、ま
た植物にも悪影響を及ぼすところから少なくとも水産物
や動植物に対する酸素供給手段としては不向きである。Further, since a metal salt such as manganese dioxide or manganese sulfate is used as a catalyst, the waste liquid after the reaction is contaminated, and the contaminated liquid kills fish and shellfish and also has an adverse effect on plants. It is not suitable as a means for supplying oxygen to at least marine products and animals and plants.
【0007】[0007]
【課題を解決するための手段】本発明は前記したよう
に、低肺機能患者の酸素吸入や、魚介類の運搬、また1
週間から1ケ月間単位での連続した酸素供給が要求され
る植物の育成用等を初めとし、多用途に用いることので
きる酸素発生剤を供給するものであり、特に酸素の発生
量および発生持続時間を自在にコントロールできるとと
もに、反応液の汚濁ならびにその有害性を取り除き、簡
便でしかも安価であり、かつ安全で確実な酸素発生剤を
得るものである。As described above, the present invention provides oxygen inhalation for patients with low lung function, transportation of seafood, and
It supplies an oxygen generating agent that can be used for a variety of purposes, such as for growing plants that require continuous oxygen supply from a week to a month, and especially for the amount of oxygen generated and its duration. It is possible to obtain a simple, inexpensive, safe, and reliable oxygen generator that can control the time freely, remove the pollution of the reaction solution and its harmfulness.
【0008】すなわち、具体的には過炭酸ソーダ、過酸
化カルシウム等の過酸化物粒子に対し、ポリエチレング
リコール等の水溶性皮膜を施してマイクロカプセル化す
るとともに、上記水溶性皮膜の外表面にカタラーゼ粒子
またはレオネットを付着させてなることを特徴とした酸
素発生剤に関する。That is, specifically, a water-soluble coating such as polyethylene glycol is applied to peroxide particles such as sodium percarbonate and calcium peroxide to form microcapsules, and catalase is formed on the outer surface of the water-soluble coating. The present invention relates to an oxygen generator characterized by being formed by adhering particles or leonets.
【0009】また本発明は、過炭酸ソーダ、過酸化カル
シウム等の過酸化物粒子に対し、ポリエチレングリコー
ル等の水溶性皮膜を施してマイクロカプセル化するとと
もに、上記水溶性皮膜の外表面にカタラーゼ粒子または
レオネットを付着させて得た粉体を、さらに錠剤化また
は顆粒化してなる酸素発生剤に関する。The present invention also provides a water-soluble coating such as polyethylene glycol on microparticles of peroxide particles such as sodium percarbonate and calcium peroxide to form microcapsules, and catalase particles on the outer surface of the water-soluble coating. Alternatively, the present invention relates to an oxygen generating agent obtained by further tableting or granulating a powder obtained by attaching Leonet.
【0010】[0010]
【作用】過炭酸ソーダ、過酸化カルシウム等のマイクロ
カプセル化された過酸化物粒子をマイクロカプセル化し
て得た酸素発生剤、もしくはその錠剤化または顆粒化さ
れた酸素発生剤は、水中に投入されると表面の水溶性皮
膜が次第に溶解して前記過酸化物が露出し、順次水に溶
解する。 一方水溶性皮膜の表面に付着させたカタラー
ゼ粒子またはレオネットが順次、上記水中に溶解した過
酸化物と反応を開始して酸素を発生し続ける。[Function] An oxygen generating agent obtained by microencapsulating peroxide particles that are microencapsulated with sodium percarbonate, calcium peroxide, or the like, or a tableted or granulated oxygen generating agent thereof is put into water. Then, the water-soluble film on the surface is gradually dissolved to expose the peroxide, and the peroxide is sequentially dissolved in water. On the other hand, the catalase particles or leonets attached to the surface of the water-soluble film sequentially start to react with the peroxide dissolved in the water to continuously generate oxygen.
【0011】したがって上記酸素発生剤を、反応容器の
形状矢、要求される酸素発生総量、使用する水の量など
の条件を考慮して、単位時間当たりの酸素発生レートを
計算し、かつ表面処理剤の溶解速度、触媒の量などをも
考慮したうえで適量投入して使用する。Therefore, the oxygen generation rate per unit time of the above oxygen generating agent is calculated in consideration of the shape of the reaction vessel, the required total amount of oxygen generation, the amount of water used, etc. Consider the dissolution rate of the agent, the amount of catalyst, etc. before adding the appropriate amount.
【0012】[0012]
【実施例】以下において、本発明の具体的な内容を実施
例をもとに説明する。 本発明において使用される酸素
発生剤としては、過炭酸ソーダ、過酸化カルシウム等の
可酸化物の粒子であり、これらは安価に入手することが
できる。EXAMPLES The specific contents of the present invention will be described below with reference to examples. The oxygen generator used in the present invention is particles of an oxidizable substance such as sodium percarbonate and calcium peroxide, and these are available at low cost.
【0013】過酸化水素付加物として過炭酸ソーダを選
択し、その反応による酸素発生のメカニズムを反応式に
より示すと次のようになる。When sodium percarbonate is selected as the hydrogen peroxide adduct and the mechanism of oxygen generation by the reaction is shown by the reaction formula as follows.
【0014】[0014]
【化1】 [Chemical 1]
【0015】上記の化学式により理解できる通り、過炭
酸ソーダに水を加えると、炭酸ナトリウムと過酸化水素
水とに解離し、触媒の存在下において過酸化水素水が水
と酸素とに分解して酸素が得られる。As can be understood from the above chemical formula, when water is added to sodium percarbonate, it is dissociated into sodium carbonate and hydrogen peroxide solution, and the hydrogen peroxide solution is decomposed into water and oxygen in the presence of a catalyst. Oxygen is obtained.
【0016】またこれらの過酸化物粒子をマイクロカプ
セル化させるための水溶性の表面被膜剤としては、ポリ
エチレングリコール、ピロリン酸ソーダ、デキストリ
ン、ボウショウ、ポバール等の使用が考えられる。 こ
れらの表面被覆剤は、前記過酸化物粒子の外表面を被覆
してマイクロカプセル化し、これによってその上に付着
させる触媒との反応を完全に遮断するとともに、大気中
の水分とも遮断することができる。As the water-soluble surface coating agent for microencapsulating these peroxide particles, use of polyethylene glycol, sodium pyrophosphate, dextrin, bowshaw, poval, etc. is considered. These surface coating agents can coat the outer surface of the above-mentioned peroxide particles to form microcapsules, thereby completely blocking the reaction with the catalyst deposited thereon and also blocking the moisture in the atmosphere. it can.
【0017】また水中に投入された場合には徐々に溶解
し、過酸化物の表面を徐々に露出させると同時に、先に
溶解する触媒との反応をコントロールし、一定量の酸素
を一定時間安定的に発生し続けることができる。When it is put into water, it gradually dissolves to gradually expose the surface of the peroxide, and at the same time controls the reaction with the catalyst that dissolves first to stabilize a certain amount of oxygen for a certain time. Can continue to occur.
【0018】また酸素発生剤を錠剤化もしくは顆粒化さ
せた場合には、その硬度を調整することにより、水中に
投入された場合に、そのミクロン単位の粒子間の反応を
安定的にコントロールして酸素発生剤の溶解速度を自在
に調整することができる。When the oxygen generating agent is tableted or granulated, the hardness thereof is adjusted to stably control the reaction between the particles in the micron unit when the oxygen generating agent is put into water. The dissolution rate of the oxygen generating agent can be adjusted freely.
【0019】さらに触媒としては、酵素のカタラーゼや
レオネットなどの使用が考えられる。 これらは水中に
おいて過炭酸ソーダなどと反応した際に、反応液の汚濁
のおそれがなく、しかも動植物に対する有害性が全くな
い。Further, as the catalyst, use of enzymes such as catalase and leonet can be considered. When they react with sodium percarbonate or the like in water, there is no risk of the reaction solution becoming contaminated, and there is no harmful effect on plants and animals.
【0020】なお、過炭酸ソーダなどの過酸化物表面に
対する触媒の固定化処理は、過酸化物の粒子を母粒子と
し、ポリエチレングリコール等の表面被覆剤を子粒子と
して、この子粒子を前記母粒子のまわりに分散させ、表
面改質化処理することにより、母粒子が皮膜で覆われて
マイクロカプセル化され、さらにその表面にカタラーゼ
等の触媒粒子を固定化する。 なおこのマイクロカプセ
ル化は、表面改質装置により、きわめて短時間に処理す
ることができる。Incidentally, in the immobilization treatment of the catalyst on the surface of the peroxide such as sodium percarbonate, the particles of the peroxide are used as the mother particles, the surface coating agent such as polyethylene glycol is used as the child particles, and the child particles are used as the mother particles. The mother particles are covered with a film to be microencapsulated by being dispersed around the particles and subjected to a surface modification treatment, and further catalyst particles such as catalase are immobilized on the surface. Note that this microencapsulation can be processed in an extremely short time by a surface modification device.
【0021】〔実験例〕 母粒子:過炭酸ソーダ(炭酸ナトリウム過酸化水素付加
物) 300〜400ミクロン 見掛比重 0.79 子粒子:ポリエチレングリコール(PEG4000) 500〜700ミクロン 上記の母粒子100グラムに対して、子粒子10グラム
を投入し、5分間の皮膜処理を施してマイクロカプセル
を得た。 その後カタラーゼ1グラムを投入して3分間
の表面改質処理をおこない、これを上記マイクロカプセ
ルの表面に付着させて酸素発生剤を得た。[Experimental example] Mother particles: sodium percarbonate (sodium carbonate hydrogen peroxide adduct) 300 to 400 microns Apparent specific gravity 0.79 Child particles: Polyethylene glycol (PEG4000) 500 to 700 microns 100 g of the above mother particles On the other hand, 10 g of child particles were added and a film treatment was performed for 5 minutes to obtain microcapsules. After that, 1 gram of catalase was added and surface modification treatment was carried out for 3 minutes.
【0022】ついで上記の酸素発生剤を、図1に示した
酸素発生装置を用いて実際の酸素発生実験をしてみた。
図1の酸素発生装置は、内部を仕切り板4により区画
して反応槽2と洗浄槽3とを形成している。 酸素発生
装置1の上部は、上蓋5により気密に、しかも取り外し
自在に構成され、かつ上蓋5には投入口6が形成されて
おり、この投入口6には蓋体7が気密に、しかも取り外
し自在に取り付けられている。Next, an actual oxygen generation experiment was conducted on the above-mentioned oxygen generator using the oxygen generator shown in FIG.
In the oxygen generator of FIG. 1, the interior is divided by a partition plate 4 to form a reaction tank 2 and a cleaning tank 3. An upper portion of the oxygen generator 1 is configured to be airtight and removable by an upper lid 5, and a charging port 6 is formed in the upper lid 5, and a lid 7 is airtightly removed from the charging port 6. It is attached freely.
【0023】反応槽2と洗浄槽3とを区画する仕切り板
4の上方には通孔8が開口され、しかも該通孔8よりチ
ューブ9により洗浄槽3の内底部付近に設置したポーラ
スストーン10に連結させている。A through hole 8 is formed above the partition plate 4 for partitioning the reaction tank 2 and the cleaning tank 3, and a porous stone 10 is installed from the through hole 8 by a tube 9 near the inner bottom of the cleaning tank 3. It is connected to.
【0024】さらに洗浄槽3に対応する前記上蓋5の一
部に通孔11が形成されており、該通孔11からチュー
ブ12により、途中除湿器13、および電子式酸素流量
計14を介してノズル15より酸素を取り出せるように
なっている。Further, a through hole 11 is formed in a part of the upper lid 5 corresponding to the cleaning tank 3, and a tube 12 is provided from the through hole 11 through an intermediate dehumidifier 13 and an electronic oxygen flow meter 14. Oxygen can be taken out from the nozzle 15.
【0025】因みに酸素発生装置1の全容積は1600
ccであり、反応層2内には900ccの水を、また洗
浄槽3内には250ccの水を入れ、投入口6より前記
した本願発明にかかる酸素発生剤を80グラム投入し
た。 酸素発生剤は反応槽内において水により表面処理
剤が徐々に溶解して過炭酸ソーダとカタラーゼが接触し
て反応を開始し、順次継続的に酸素を発生し続ける。Incidentally, the total volume of the oxygen generator 1 is 1600.
cc, 900 cc of water was put in the reaction layer 2, 250 cc of water was put in the cleaning tank 3, and 80 g of the above-mentioned oxygen generating agent according to the present invention was put through the inlet 6. In the oxygen generator, the surface treatment agent is gradually dissolved by water in the reaction tank, sodium percarbonate and catalase come into contact with each other to start a reaction, and oxygen is continuously and continuously generated.
【0026】反応室2の上部には酸素が溜まり、その圧
力により通孔8からチューブ9を通じて洗浄室内に送り
込まれ、ポーラスストーン10により微細な気泡となっ
て洗浄槽3の内底部より放出される。 さらに放出され
た気泡は水中を上昇しながら炭酸ソーダのミスト等の不
純物が除去されて通孔11よりさらにチューブ12を伝
い、除湿器13を通過する際に水分を除去されて取り出
しノズル15へと送られる。 なお途中電子式酸素流量
計14を通過することにより、その流量がデジタル表示
される。Oxygen collects in the upper part of the reaction chamber 2 and is sent into the cleaning chamber from the through hole 8 through the tube 9 by the pressure thereof, and becomes fine bubbles by the porous stone 10 and is discharged from the inner bottom part of the cleaning tank 3. . Further, the released bubbles rise in the water and impurities such as mist of sodium carbonate are removed and are further transmitted through the tube 12 through the through hole 11. When passing through the dehumidifier 13, the water is removed and the bubbles are taken out to the extraction nozzle 15. Sent. By passing the electronic oxygen flow meter 14 on the way, the flow rate is digitally displayed.
【0027】上記の酸素流量計14により経時的に酸素
の流量を測定し、同時に水温の上昇変化を測定した。
結果を反応液および洗浄液の温度が異なる毎に表1から
表5に示す。The oxygen flowmeter 14 was used to measure the oxygen flow rate over time, and at the same time, the change in water temperature was measured.
The results are shown in Tables 1 to 5 every time the temperature of the reaction solution and the temperature of the cleaning solution are different.
【0028】[0028]
【表1】 [Table 1]
【0029】[0029]
【表2】 [Table 2]
【0030】[0030]
【表3】 [Table 3]
【0031】[0031]
【表4】 [Table 4]
【0032】[0032]
【表5】 [Table 5]
【0033】[0033]
【発明の効果】本発明は上記した通り、過炭酸ソーダ、
過酸化カルシウム等の過酸化物粒子に対し、水溶性皮膜
を施してマイクロカプセル化するとともに、上記水溶性
皮膜の外表面にカタラーゼ粒子またはレオネットを付着
させてなるものであるために、従来のように酸素発生剤
と触媒とを別個に密封分包して保管・使用する必要がな
く、しかも使用に際しては、単に上記酸素発生剤を水中
に投入するだけの簡単な操作で長時間にわたる安定した
酸素の供給を行うことができる。As described above, the present invention provides a sodium percarbonate,
With respect to peroxide particles such as calcium peroxide, a water-soluble film is applied to form microcapsules, and catalase particles or leonets are attached to the outer surface of the water-soluble film. As described above, it is not necessary to separately store and use the oxygen generating agent and the catalyst separately in a sealed package, and at the time of use, stable operation can be achieved for a long period of time by simply inserting the oxygen generating agent into water. Oxygen can be supplied.
【0034】またマイクロカプセル化した水溶性皮膜の
外表面に触媒を付着させて得た粉体を、さらに錠剤化ま
たは顆粒化することにより、酸素の発生量および発生継
続時間を自在にコントロールでき、しかも触媒としてカ
タラーゼまたはレオネットを用いるために、特に反応液
の汚濁、ならびに動植物に対する有害性がなく、その結
果緊急患者をはじめとした病人や、酸素補給を必要とす
る人、または魚介類の輸送や植物の育成をはじめとし、
多用途に用いることができる。 さらに原材料が安価で
あり、かつ安全性が高く、しかも確実な酸素発生を可能
とする等種々の有益な効果を奏する。By further tableting or granulating the powder obtained by adhering the catalyst to the outer surface of the microcapsulated water-soluble film, the amount of oxygen generation and the duration of generation can be freely controlled, Moreover, since catalase or leonet is used as a catalyst, there is no pollution of the reaction solution and no harmful effects on plants and animals, and as a result, transportation of sick people such as emergency patients, people who need supplemental oxygen, or seafood. And growing plants,
It can be used for multiple purposes. Furthermore, the raw materials are inexpensive, the safety is high, and various beneficial effects such as reliable oxygen generation are achieved.
【図1】本発明における酸素発生剤の実験的使用に供さ
れた酸素発生装置の縦断面図。FIG. 1 is a vertical cross-sectional view of an oxygen generator provided for experimental use of an oxygen generator according to the present invention.
1 酸素発生装置 2 反応槽 3 洗浄槽 4 仕切り板 5 上蓋 6 投入口 7 蓋体 8 通孔 9 チューブ 10 ポーラスストーン 11 通孔 12 チューブ 13 除湿器 14 電子式酸素流量計 15 ノズル DESCRIPTION OF SYMBOLS 1 Oxygen generator 2 Reaction tank 3 Washing tank 4 Partition plate 5 Upper lid 6 Input port 7 Lid body 8 Through hole 9 Tube 10 Porous stone 11 Through hole 12 Tube 13 Dehumidifier 14 Electronic oxygen flow meter 15 Nozzle
Claims (2)
酸化物粒子に対し、水溶性皮膜を施してマイクロカプセ
ル化するとともに、上記水溶性皮膜の外表面にカタラー
ゼ粒子またはレオネットを付着させてなることを特徴と
した酸素発生剤。1. A water-soluble coating is applied to peroxide particles such as sodium percarbonate and calcium peroxide to form microcapsules, and catalase particles or leonets are attached to the outer surface of the water-soluble coating. Oxygen generator characterized in that
酸化物粒子に対し、水溶性皮膜を施してマイクロカプセ
ル化するとともに、上記水溶性皮膜の外表面にカタラー
ゼ粒子またはレオネットを付着させて得た粉体を、さら
に錠剤化または顆粒化してなる酸素発生剤。2. A water-soluble coating is applied to peroxide particles such as sodium percarbonate and calcium peroxide to form microcapsules, and catalase particles or leonets are attached to the outer surface of the water-soluble coating. An oxygen generating agent obtained by tableting or granulating the obtained powder.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP05390791A JP3191817B2 (en) | 1991-02-26 | 1991-02-26 | Oxygen generator |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP05390791A JP3191817B2 (en) | 1991-02-26 | 1991-02-26 | Oxygen generator |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06107401A true JPH06107401A (en) | 1994-04-19 |
| JP3191817B2 JP3191817B2 (en) | 2001-07-23 |
Family
ID=12955790
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP05390791A Expired - Fee Related JP3191817B2 (en) | 1991-02-26 | 1991-02-26 | Oxygen generator |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3191817B2 (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0788806A3 (en) * | 1996-01-22 | 1998-04-22 | Gertraud Canavate Riera | Agent for releasing oxigen in an oxigen generator |
| US6267114B1 (en) | 1998-05-14 | 2001-07-31 | Hoshiko Inc. | Handy oxygen generator |
| JP2006131455A (en) * | 2004-11-05 | 2006-05-25 | Mitsubishi Gas Chem Co Inc | Sodium percarbonate particles with excellent foam solubility |
| JP2007523816A (en) * | 2003-05-30 | 2007-08-23 | クラウス・シェヒティング | Method for supplying oxygen to a biologically utilized aqueous system and apparatus and set for carrying out said method |
| WO2018124122A1 (en) | 2016-12-28 | 2018-07-05 | ユニ・チャーム株式会社 | Absorbent article |
| CN110121322A (en) * | 2016-12-28 | 2019-08-13 | 尤妮佳股份有限公司 | Absorbent commodity |
| US10493040B2 (en) * | 2007-04-09 | 2019-12-03 | Wake Forest University Health Sciences | Oxygen-generating compositions for enhancing cell and tissue survival in vivo |
| WO2020150588A1 (en) * | 2019-01-18 | 2020-07-23 | Lifecell Corporation | Time-delayed cross-linking of tissue fillers and applications thereof |
| CN112125279A (en) * | 2020-09-21 | 2020-12-25 | 湖南可孚医疗设备有限公司 | Mixed oxygen generating agent and preparation method thereof |
-
1991
- 1991-02-26 JP JP05390791A patent/JP3191817B2/en not_active Expired - Fee Related
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0788806A3 (en) * | 1996-01-22 | 1998-04-22 | Gertraud Canavate Riera | Agent for releasing oxigen in an oxigen generator |
| US6267114B1 (en) | 1998-05-14 | 2001-07-31 | Hoshiko Inc. | Handy oxygen generator |
| JP2007523816A (en) * | 2003-05-30 | 2007-08-23 | クラウス・シェヒティング | Method for supplying oxygen to a biologically utilized aqueous system and apparatus and set for carrying out said method |
| JP2006131455A (en) * | 2004-11-05 | 2006-05-25 | Mitsubishi Gas Chem Co Inc | Sodium percarbonate particles with excellent foam solubility |
| US10493040B2 (en) * | 2007-04-09 | 2019-12-03 | Wake Forest University Health Sciences | Oxygen-generating compositions for enhancing cell and tissue survival in vivo |
| US10493041B2 (en) | 2007-04-09 | 2019-12-03 | Wake Forest University Health Sciences | Oxygen-generating compositions for enhancing cell and tissue survival in vivo |
| US11318106B2 (en) | 2007-04-09 | 2022-05-03 | Wake Forest University Health Sciences | Oxygen-generating compositions for enhancing cell and tissue survival in vivo |
| WO2018124122A1 (en) | 2016-12-28 | 2018-07-05 | ユニ・チャーム株式会社 | Absorbent article |
| CN110121322A (en) * | 2016-12-28 | 2019-08-13 | 尤妮佳股份有限公司 | Absorbent commodity |
| US11433157B2 (en) | 2016-12-28 | 2022-09-06 | Unicharm Corporation | Absorbent article |
| WO2020150588A1 (en) * | 2019-01-18 | 2020-07-23 | Lifecell Corporation | Time-delayed cross-linking of tissue fillers and applications thereof |
| CN112125279A (en) * | 2020-09-21 | 2020-12-25 | 湖南可孚医疗设备有限公司 | Mixed oxygen generating agent and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3191817B2 (en) | 2001-07-23 |
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