JPS6140803A - Flocculation-like chlorine dioxide generating composition and its packing body - Google Patents
Flocculation-like chlorine dioxide generating composition and its packing bodyInfo
- Publication number
- JPS6140803A JPS6140803A JP16271684A JP16271684A JPS6140803A JP S6140803 A JPS6140803 A JP S6140803A JP 16271684 A JP16271684 A JP 16271684A JP 16271684 A JP16271684 A JP 16271684A JP S6140803 A JPS6140803 A JP S6140803A
- Authority
- JP
- Japan
- Prior art keywords
- chlorine dioxide
- generating composition
- water
- coagulated
- aqueous solution
- 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
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
(Ill上上利用分野)
不発明は二酸化塩素ガスを安定した状態で長時間安全に
放出させ、効率良(脱臭、滅菌を行うことかできる凝固
状二酸化塩素発生組成物及びその包装体に関するもので
ある。Detailed Description of the Invention (Ill. Field of Application) The invention is a coagulated chlorine dioxide generating composition that can safely release chlorine dioxide gas in a stable state for a long period of time and can perform efficient deodorization and sterilization. and its packaging.
(従来の技術)
従来の脱臭剤は主として吸着性を有する物質、例え、ば
活性炭、活性白土シリカゲル等が用いられ、脱臭領内で
自然の状態で臭の分子を吸着せしめるものでめった・
従って、その脱^効果は十分なものでなく、時間と共に
吸着能力は低下し、温度変化により、例えば温度が上昇
した場合には、吸着物を逆に放出してしまうという欠点
がるり、aIn理的な吸着作用のみで滅菌効果は認めら
れなかった。(Prior art) Conventional deodorizers mainly use adsorbent substances, such as activated carbon and activated clay silica gel, which naturally adsorb odor molecules within the deodorizing area. The desorption effect is not sufficient, and the adsorption capacity decreases over time. Due to temperature changes, for example, when the temperature rises, the adsorbate is released instead. No sterilization effect was observed.
従って、これらに代って二酸化塩素を利用する方法か考
えられているが、しかしながら二酸化塩素は不安定な危
険物で、看しい爆発生がるり、多くの物質と激しく反応
し、塩素のが倍の有効塩素量を有する強力な酸化剤で一
般に必要な場所での使用は困難な上、技術的にも高度な
設備と優れた技術を必要とするので、大量に使用する場
合には事業所で自家発生を行っている。Therefore, the use of chlorine dioxide has been considered as an alternative to these, but chlorine dioxide is an unstable and dangerous substance, can cause serious explosions, reacts violently with many substances, and is twice as strong as chlorine. It is a strong oxidizing agent with an effective chlorine content of Self-generated.
また貯蔵並びに容易に輸送され、必要に応じて安全にし
て簡単に使用できる二酸化塩素の研究が行われ、安定し
た二酸化塩素水溶液が開発され、危険性のない安定化二
酸化塩素4%の水溶液の使用時に適度な濃度に稀釈して
使用するか、安定化二酸化塩素水溶液を多大質物質のゼ
オライト等に含浸させ、粉体状態で使用されているのが
央情である。Research has also been carried out on chlorine dioxide, which can be easily stored and transported, and is safe and easy to use when needed. A stable aqueous solution of chlorine dioxide has been developed, and the use of a non-hazardous stabilized 4% aqueous solution of chlorine dioxide has been carried out. Generally, it is used diluted to an appropriate concentration, or in powdered form by impregnating a stabilized aqueous solution of chlorine dioxide into a macromaterial such as zeolite.
しかし粉では製造工程で複雑であり、製品の包装に手間
がか\す、濃度の異なる製品を均一に造ることが出来ず
、二酸化塩素ガスを長時間均一に放出することが困難で
るり、また使用中粉末によって器材その他が汚染される
こともるり、取扱上の欠点がるり、これら欠点を除去す
る方法として特開昭57−22102号の如き二酸化塩
素水を寒天、ゼラチンなどのゲル化剤でゲル化した状態
で使用しているものが知られている=
(発明が解決しようとする問題点)
しかし、このようにゲル化した状態のものは低温におけ
る二酸化塩素の蒸発速度が遅(、冷蔵庫などにおける脱
臭効果及び滅菌効果が悪く、また高温状態における変形
、ないしは融解か起り、盛夏期での例えば自動車内等に
使用する場合に脱臭効果か低下するなどの欠点かめる。However, with powder, the manufacturing process is complicated, it takes time to package the product, it is impossible to make products with different concentrations uniformly, it is difficult to release chlorine dioxide gas uniformly over a long period of time, and In order to eliminate the contamination of instruments and other objects by the powder during use, as well as the disadvantages of handling, a method of removing chlorine dioxide water with a gelling agent such as agar or gelatin as described in JP-A No. 57-22102 is proposed. It is known that chlorine dioxide is used in a gelled state = (Problem to be solved by the invention) However, in this gelled state, the evaporation rate of chlorine dioxide is slow at low temperatures (and It has disadvantages such as poor deodorizing and sterilizing effects, and deformation or melting at high temperatures, which reduces the deodorizing effect when used in, for example, automobiles in midsummer.
(発明の目的)
これら欠点に鑑み、二酸化塩素ガスを安定した状態で長
時間安全に放出させ効率良(脱臭。(Objective of the invention) In view of these drawbacks, chlorine dioxide gas can be released safely for a long time in a stable state with high efficiency (deodorization).
滅菌を有効に行うことができるように、液状安定化二酸
化塩素水溶液を高吸水性樹脂に吸収させ【凝固状態にし
、冷蔵庫内の如き低温時でも盛夏の自動車内の高温の場
合でも凝固状態を保持する凝固状二酸化塩素発生組成物
及び包装体を提供せんとするものである。In order to effectively perform sterilization, a liquid stabilized chlorine dioxide aqueous solution is absorbed into a super absorbent resin and turned into a coagulated state, which maintains its coagulated state even at low temperatures such as inside a refrigerator or at high temperatures inside a car in midsummer. It is an object of the present invention to provide a coagulated chlorine dioxide generating composition and a package.
(発明の構成)
その要旨とするところは、高分子化合物高吸水性樹脂と
水と二数化塩素含有水溶液と接着剤より凝固状に形成し
、該凝′固状より安定状態で発生する二酸化塩素を拡散
せしめるようにした凝固状二酸化塩素発生組成物及びそ
の包装体にるる。(Structure of the Invention) The gist of the invention is to form a coagulated state from a polymer compound superabsorbent resin, water, a divalent chlorine-containing aqueous solution, and an adhesive, and to generate carbon dioxide in a stable state from the solidified state. A coagulated chlorine dioxide generating composition and a package thereof for diffusing chlorine are provided.
而して凝固状二酸化塩素発生組成物の製造方法を以下詳
細に説明する。The method for producing the coagulated chlorine dioxide generating composition will now be described in detail.
二酸化塩素の化学的性質の一つとして二重結合部分並び
にベンゼン核等には強力忙反応し、その他シアン化合資
、硫化水素、ホルムアルデヒド、フェノール化合吻、蛋
白質等とも反応するか、デン粉系、セルローズ系並びに
合成ポリマー系重合体のような高分子化合物高吸水性樹
脂は容易に反応しない性質かめる。One of the chemical properties of chlorine dioxide is that it reacts strongly with double bonds and benzene nuclei, and also reacts with other substances such as cyanide, hydrogen sulfide, formaldehyde, phenolic compounds, proteins, starch, etc. High-molecular compound superabsorbent resins such as cellulose-based and synthetic polymer-based polymers do not react easily.
ことに言う高分子化合物高吸水性樹脂とは具体的には例
えば澱粉系ではポリマーA−100(粉末〕、サンウェ
ット〔粉末〕、セルローズ系゛ではAguaron C
#錐状) 、 AkuceJJ (l)末〕。Specifically, the polymer compound superabsorbent resin mentioned above includes, for example, Polymer A-100 (powder) and Sunwet (powder) for starch-based products, and Aguaron C for cellulose-based products.
#AkuceJJ (l) terminal].
合成ポリマー系ではDowaJ (シート状〕、ワンダ
ーゲル〔粉末〕、スミカゲル〔粉末〕、アクアキープ〔
粉末) 、 Fa Bor (粉末〕、クラレゲル〔粉
末〕、に1ゲル〔粉末〕、アラソープ〔粉末〕などを言
う。Synthetic polymers include DowaJ (sheet form), Wonder Gel [powder], Sumikagel [powder], and Aqua Keep [
powder), Fa Bor (powder), Kuraraygel [powder], Ni 1 Gel [powder], Arasop [powder], etc.
この高分子化合物高吸水性樹脂とは容易に反応しない特
性を利用して、二酸化塩素水溶液を規定のPHと規定の
濃度K11l整し、常温で攪拌し、規定量の高分子高吸
水性樹脂を分散混入する。Utilizing the property of this polymer compound that does not easily react with the super absorbent resin, adjust the chlorine dioxide aqueous solution to the specified pH and concentration K11l, stir at room temperature, and add the specified amount of the polymer super absorbent resin. Distribute and mix.
混入後2〜3分間内に二酸化塩素水溶液は高吸水性樹脂
に吸水され、凝固状態物質に変る。Within 2 to 3 minutes after being mixed in, the chlorine dioxide aqueous solution is absorbed by the superabsorbent resin and turns into a solidified substance.
高吸水性樹脂がフィルム状又は繊維状の樹脂を使用する
場合は、使用目的に従って、攪拌することなしに、逆く
に安定化二酸化塩素水溶液を高吸水性−脂の方に注入し
て凝固状態物質を形成する。When using a film-like or fibrous superabsorbent resin, a stabilized chlorine dioxide aqueous solution is injected into the superabsorbent fat side without stirring, depending on the purpose of use, to form a solidified state material. form.
高分子高吸水性樹脂は粒状で接着力が弱゛^ので、デン
粉、セルローズ、合成ポリマーの各々を混合し接着力を
高めることかできるが安全であるとは言えなho
従って安定化二酸化塩素水を#に収した高吸水樹脂粒子
を粒子間で接着する目的で接着剤を用いることが必要で
ある。Polymer superabsorbent resin is granular and has weak adhesive strength, so it is possible to increase the adhesive strength by mixing starch, cellulose, and synthetic polymers, but it cannot be said to be safe. Therefore, stabilized chlorine dioxide It is necessary to use an adhesive for the purpose of adhering the super absorbent resin particles containing water to each other between the particles.
このための接着剤としては、澱粉質類、動植物蛋白質類
、海藻原料製品類、セルローズ誘導物質類等を用い、高
吸水性樹脂粒子を谷々接層することにより、粘匿の高い
凝固状態物質を得ることを特徴とするものである。For this purpose, starches, animal and plant proteins, seaweed raw material products, cellulose-inducing substances, etc. are used as adhesives, and super-absorbent resin particles are layered in layers to form a highly viscous coagulated state material. It is characterized by obtaining the following.
凝固状態の硬軟は接着剤及び水の添加割合によって加減
することができ、所望する状態を容易に達成することが
できる。The hardness or softness of the solidified state can be adjusted by adjusting the addition ratio of adhesive and water, and a desired state can be easily achieved.
また安定化二酸化塩素を保つためにはPHを保持しなけ
ればならず、そのためには例えばIIk度40.000
PPm o水溶液−eはPH9’に保nfb必要がめる
。In addition, in order to maintain stabilized chlorine dioxide, the pH must be maintained, for example, at IIk degree of 40.000.
The PPmO aqueous solution-e needs to be kept at pH 9'.
PH濃度の変化によって安定性が変化し、PHが小さく
なるにしたがって不安定となり、二酸化塩素か多(遊離
する。Stability changes with changes in pH concentration, and as the pH decreases, it becomes unstable and more chlorine dioxide is liberated.
一般に家庭並びに業界で使用する安定化二酸化塩素の濃
度は20〜5.000PPm程度低濃度の液剤として使
用されている。Generally, stabilized chlorine dioxide used at home and in industry is used as a low-concentration solution of about 20 to 5,000 PPm.
このように安定化二酸化塩素の濃度を下げるとPH7に
近づき安定化の手術か破れて不安定となる。If the concentration of stabilized chlorine dioxide is lowered in this way, the pH will approach 7, and the stabilization process will be broken, resulting in instability.
この不安定となるのを防ぐためにPH9に保ち続ける必
要かめる。To prevent this instability, it is necessary to keep the pH at 9.
次に安定化二酸化塩素を吸収した高分子高吸水性樹脂の
凝固状態物質を充填する容器包装体について、高分子高
吸水性樹脂は日光に対する強度は弱く、精製水をWk収
した高吸水性樹脂を透明ポリ容器に入れて、日光に曝す
と16時間位で糊状の粘度の高い液体状態に変り時間の
経過するに従って粘度は減少して行く。Next, regarding containers and packages filled with a solidified material of polymeric superabsorbent resin that has absorbed stabilized chlorine dioxide, polymeric superabsorbent resin has low resistance to sunlight, and superabsorbent resin that has absorbed purified water Wk. When placed in a transparent plastic container and exposed to sunlight, it changes to a pasty, highly viscous liquid state in about 16 hours, and the viscosity decreases as time passes.
この現象は高吸水性樹脂に安定化二酸化塩素水溶液を吸
収させた場合も同じ状態を示す。The same phenomenon occurs when the superabsorbent resin absorbs a stabilized chlorine dioxide aqueous solution.
この現象は高分子化合物か元エネルギーにより分解され
るものと考えられる。This phenomenon is thought to be due to the decomposition of the polymer compound due to its original energy.
何故ならば熱による変化試験をした結果、安定化二酸化
塩素水溶液をg&収した高吸水性樹脂を透明ポリ容器に
入れて密閉定温加熱器で50℃。This is because, as a result of a heat-induced change test, the super absorbent resin containing 1 g of a stabilized chlorine dioxide aqueous solution was placed in a transparent polyethylene container and heated to 50°C in a closed constant temperature heater.
60℃、10℃、80℃、85℃と各温度で24時間加
熱試駿を行ったもので、その結果85℃で変形。A 24-hour heating test was conducted at 60°C, 10°C, 80°C, and 85°C, and as a result, it deformed at 85°C.
融解1分解等の変化は起きなかった。すなわち熱による
分解反応では無く、光による分解反応である。No changes such as melting and decomposition occurred. In other words, it is not a decomposition reaction due to heat, but a decomposition reaction due to light.
また充填用透明ポリ容器を銀色、黒色、赤褐色、赤色、
黄色、緑色、青色に塗装して、各色の容器に安定化二酸
化塩素水溶液を吸収した高吸水性樹脂を充填して、日光
に曝すと銀色、黒色、赤褐色、赤色、黄色等の容器では
分解反応は起きないが、緑色、青色等では分解反応が徐
々に起きた。We also offer transparent plastic containers for filling in silver, black, reddish-brown, and red.
Painted yellow, green, and blue, containers of each color are filled with super absorbent resin that has absorbed a stabilized chlorine dioxide aqueous solution, and when exposed to sunlight, silver, black, reddish brown, red, yellow, etc. containers decompose. did not occur, but decomposition reactions occurred gradually in green, blue, etc.
そこで安定化二酸化塩素水溶液を高吸水性樹脂に吸取せ
しめた凝固物の充填容器は遮光性容器を用いて高吸水性
樹脂の分解を防止する必要がめる。Therefore, it is necessary to use a light-shielding container to prevent decomposition of the superabsorbent resin in a container filled with a coagulated product in which a stabilized chlorine dioxide aqueous solution is absorbed by a superabsorbent resin.
従って遮光性容器に充填した安定化二酸化塩素水溶液を
吸収した高吸水性樹脂凝固物は直射日光iされた自動車
内の84℃の場所に置いても融解9分、解勢の反応は起
きず、明るく高温の場所に保存すること、並びに光に熱
に耐えて使用されるのか第2の特徴である。Therefore, even if a superabsorbent resin coagulated material that has absorbed a stabilized chlorine dioxide aqueous solution filled in a light-shielding container is placed in a place exposed to direct sunlight at 84°C in a car, it will melt for 9 minutes and no decomposition reaction will occur. The second characteristic is that it must be stored in a bright and hot place, and that it can withstand light and heat.
すなわち盛夏期に自動車内の84℃にもなる場所に置い
′cJli−内の脱臭に使用することができるといろこ
とである。That is, it can be used to deodorize the inside of a car by placing it in a place where the temperature can reach 84°C in midsummer.
この第2の発明である包装体について説明すると、!1
図及び第2図に示すように高分子化合物高吸水性樹脂と
水と二は化塩素含有水溶液と接着剤より成る凝固状組成
物1を少(とも一方に開口部2を有する容器3に充填し
、使用の際に開口部2を開放するものである。This second invention, the package, will be explained below! 1
As shown in Figures 1 and 2, a small amount of a coagulated composition 1 consisting of a polymeric superabsorbent resin, water, a chlorine-containing aqueous solution, and an adhesive is filled into a container 3 having an opening 2 on one side. The opening 2 is opened during use.
容器3はガラス、プラスチック、金属等の任意の素材で
形成されたものを利用することができ、容器3は透明容
器については銀色1M色。The container 3 can be made of any material such as glass, plastic, metal, etc. If the container 3 is transparent, it is 1M silver in color.
赤褐色等に着色して遮光性容器とする必要かめるO
開口部2は図面から明らかなように、容器30口部に装
着する蓋4に設けるのが便利である。As is clear from the drawing, it is convenient to provide the opening 2 in the lid 4 attached to the mouth of the container 30.
なお蓋4の内側には不使用時に二酸化塩素発生溶液の逸
散を防止するように内蓋5t−容器3に嵌合する。An inner lid 5t is fitted inside the lid 4 to the container 3 to prevent the chlorine dioxide generating solution from escaping when not in use.
前記開口部2は蓋4に設けないで、円蓋5に設は蓋4を
密閉蓋として使用するように構成してもよい。The opening 2 may not be provided in the lid 4, but may be provided in the dome 5, and the lid 4 may be used as a sealing lid.
このように構成することにより、開口部2を開口状態に
して使用目的に応じた場所に設置することにより、有効
成分を拡散させて殺菌、脱臭等を行うことができる。With this configuration, the active ingredient can be diffused to perform sterilization, deodorization, etc. by leaving the opening 2 in an open state and installing it at a location depending on the purpose of use.
また容器の形状を変化させることにより、各種の場所に
設置することも可能でめる。Also, by changing the shape of the container, it can be installed in various locations.
(実施例)
安定化二酸化塩素含有量4万PPm水溶液O250ma
に水750rrMlを加えて攪拌し、1.000mJの
水溶液を作り、これに5gの色素を加えて着色する。(Example) Stabilized chlorine dioxide content 40,000 PPm aqueous solution O250ma
Add 750rrMl of water and stir to make a 1.000mJ aqueous solution, and add 5g of dye to this for coloring.
PH測測定結果、必要がめれば炭酸ナトリウムを加えズ
PHを9に調整する。Based on the pH measurement results, if necessary, add sodium carbonate to adjust the pH to 9.
講義された5、OOOPPm含有の安定化二酸化塩素水
溶液の100mJを10個の遮光充填容器に各々に注入
し、各溶液を攪拌しながら、高吸水性樹脂の2gを加え
、良く攪拌混合して攪拌を止める。Lecture 5. Pour 100 mJ of stabilized chlorine dioxide aqueous solution containing OOOPPm into 10 light-shielding filled containers, add 2 g of super absorbent resin while stirring each solution, and mix well. stop.
1分〜2分間後に安定化二酸化塩素水溶液は高吸水性樹
脂に@収され、凝固状態に変り、製品が得られる。After 1 to 2 minutes, the stabilized chlorine dioxide aqueous solution is absorbed into the superabsorbent resin, turns into a solidified state, and a product is obtained.
(発明の効果)
高分子高吸水性樹脂に@収された安定化二酸化塩素水溶
液の凝固物は寒天凝固剤による凝固物又は脂肪酸ナトリ
ウム塩凝固剤による凝固物に比べ高吸水性樹脂による吸
収凝固状物は粒子の集合体であるため、表面積が太き(
蒸散速度は大きくなる。(Effects of the invention) The coagulation of the stabilized chlorine dioxide aqueous solution absorbed in the polymeric superabsorbent resin is more like a coagulated material absorbed by the superabsorbent resin than that of the agar coagulant or the fatty acid sodium salt coagulant. Since objects are aggregates of particles, they have a large surface area (
The transpiration rate increases.
冷蔵庫内の5℃の温度の場合、高吸水性樹脂の蒸発減量
1.2〜1.4gに対し、他の凝固剤の場合は0.3g
〜0.5gで蒸発減量は少ない。At a temperature of 5°C in the refrigerator, the evaporation loss of super absorbent resin is 1.2 to 1.4 g, while that of other coagulants is 0.3 g.
The evaporation loss is small at ~0.5g.
これに対して高吸水性樹脂を用いた場合、冷蔵庫内の二
酸化塩素の蒸散量が多くなり、脱臭効果並itjI4m
効果を高めることができた。On the other hand, when super absorbent resin is used, the amount of transpiration of chlorine dioxide inside the refrigerator increases, and the deodorizing effect is reduced.
I was able to increase the effectiveness.
また高温日光下でも分解反応差に融解等を起さないので
、盛夏の直射日光下の自動車内の84℃の場所に置いて
も使用することが出来る。Furthermore, since no melting occurs due to the difference in decomposition reaction even under high-temperature sunlight, it can be used even when placed in a car at 84° C. under direct sunlight in midsummer.
更に保存する場合、特に冷、暗所に保管する必要がな(
なり、安全で清潔で保管、運搬、使用場所の簡易さ、危
険などはなく、安心して使用することが出来、従来の製
品より2.5倍の効果を発揮することができる特徴かめ
9、冷蔵庫。If you want to store it further, there is no need to store it in a cool, dark place (
It is safe, clean, easy to store, transport, and use, there is no danger, and it can be used with peace of mind, and is 2.5 times more effective than conventional products. .
食器戸棚、生鮮食品ショーケース、食品保管庫。Cupboards, fresh produce showcases, food storage.
はツカ−9室内、トイレ、下駄箱等その他山動車等のろ
らゆる閉成部分に適用される。This applies to the Tsuka-9 interior, toilets, shoe cabinets, and other closed parts of mountain vehicles.
%にタクシ−の場合先客の体臭を消し、次の客に清潔感
を与えると共に、冷蔵庫内の生鮮食品の鮮度保持に顕著
な効果を示す。In the case of taxis, it eliminates the body odor of the previous passenger, giving the next passenger a sense of cleanliness, and has a remarkable effect on preserving the freshness of fresh food stored in the refrigerator.
・ 第1図は本発明に係る凝固状二酸化塩素発生組成
物包装体の一部切欠き正面図、第2図は同発明の斜視図
である。
1・・−M固状組成物、2・・・開口部、3・・・容器
、4・・・葺、5・・・内蓋。- FIG. 1 is a partially cutaway front view of a packaged solidified chlorine dioxide generating composition according to the present invention, and FIG. 2 is a perspective view of the same invention. 1...-M solid composition, 2... Opening, 3... Container, 4... Roof, 5... Inner lid.
Claims (4)
水溶液と接着剤より凝固状に形成し、該凝固状より安定
状態で発生する二酸化塩素を拡散せしめるように形成し
たことを特徴とする凝固状二酸化塩素発生組成物。(1) It is characterized in that it is formed into a coagulated form from a polymeric compound, a superabsorbent resin, water, an aqueous solution containing chlorine dioxide, and an adhesive, and is formed in such a way that the chlorine dioxide generated in a stable state is diffused from the coagulated form. Solidified chlorine dioxide generating composition.
ズ系、及び合成ポリマー系の重合体である特許請求の範
囲第1項記載の凝固状二酸化塩素発生組成物。(2) High molecular compound The coagulated chlorine dioxide generating composition according to claim 1, wherein the superabsorbent resin is a starch-based, cellulose-based, or synthetic polymer-based polymer.
導体である特許請求の範囲第1項記載の凝固状二酸化塩
素発生組成物。(3) The coagulated chlorine dioxide generating composition according to claim 1, wherein the adhesive is starch, protein, or a cellulose derivative of seaweed products.
水溶液と接着剤よりなる凝固状二酸化塩素発生組成物を
少くとも一部開口部を設けた容器に充填したことを特徴
とする凝固状二酸化塩素発生組成物包装体。(4) A coagulated chlorine dioxide generating composition comprising a superabsorbent polymer compound, water, an aqueous solution containing chlorine dioxide, and an adhesive is filled in a container having at least a partial opening. Chlorine dioxide generating composition packaging.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16271684A JPS6140803A (en) | 1984-07-31 | 1984-07-31 | Flocculation-like chlorine dioxide generating composition and its packing body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16271684A JPS6140803A (en) | 1984-07-31 | 1984-07-31 | Flocculation-like chlorine dioxide generating composition and its packing body |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6140803A true JPS6140803A (en) | 1986-02-27 |
Family
ID=15759933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16271684A Pending JPS6140803A (en) | 1984-07-31 | 1984-07-31 | Flocculation-like chlorine dioxide generating composition and its packing body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6140803A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008099911A1 (en) | 2007-02-16 | 2008-08-21 | Taiko Pharmaceutical Co., Ltd. | Broad-spectrum antiviral composition having excellent storage stability |
WO2008111357A1 (en) | 2007-03-15 | 2008-09-18 | Taiko Pharmaceutical Co., Ltd. | Pure chlorine dioxide solution, and gel-like composition and foamable composition each comprising the same |
WO2008117767A1 (en) | 2007-03-27 | 2008-10-02 | Taiko Pharmaceutical Co., Ltd. | Therapeutic agent for infectious skin or mucosal disease |
JP2011246298A (en) * | 2010-05-25 | 2011-12-08 | Amatera:Kk | Chlorine dioxide gas generation and release vessel and chlorine dioxide gas generation and release method using the same |
JP2012011028A (en) * | 2010-07-01 | 2012-01-19 | Yoshinori Matsuyama | Slowly releasing implement for chlorine dioxide gas |
CN102388919A (en) * | 2011-10-17 | 2012-03-28 | 华中农业大学 | Soil composite disinfectant and using method thereof |
JP2012147852A (en) * | 2011-01-17 | 2012-08-09 | Safe Section Inc | Chlorine dioxide controlled releasing agent, and chlorine dioxide controlled releasing agent contained in container |
JP2014025064A (en) * | 2012-07-24 | 2014-02-06 | Hao-Chang Yin | Chlorine dioxide gel and method for manufacturing the same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57153736A (en) * | 1981-03-16 | 1982-09-22 | Enkuraa Bijinesu:Kk | Moisture absorbing sheet having deodorizing capacity |
JPS5946962A (en) * | 1982-09-10 | 1984-03-16 | 株式会社 エンクラ−ビジネス | Deodorant composition |
-
1984
- 1984-07-31 JP JP16271684A patent/JPS6140803A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57153736A (en) * | 1981-03-16 | 1982-09-22 | Enkuraa Bijinesu:Kk | Moisture absorbing sheet having deodorizing capacity |
JPS5946962A (en) * | 1982-09-10 | 1984-03-16 | 株式会社 エンクラ−ビジネス | Deodorant composition |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008099911A1 (en) | 2007-02-16 | 2008-08-21 | Taiko Pharmaceutical Co., Ltd. | Broad-spectrum antiviral composition having excellent storage stability |
WO2008111357A1 (en) | 2007-03-15 | 2008-09-18 | Taiko Pharmaceutical Co., Ltd. | Pure chlorine dioxide solution, and gel-like composition and foamable composition each comprising the same |
WO2008117767A1 (en) | 2007-03-27 | 2008-10-02 | Taiko Pharmaceutical Co., Ltd. | Therapeutic agent for infectious skin or mucosal disease |
JP2011246298A (en) * | 2010-05-25 | 2011-12-08 | Amatera:Kk | Chlorine dioxide gas generation and release vessel and chlorine dioxide gas generation and release method using the same |
JP2012011028A (en) * | 2010-07-01 | 2012-01-19 | Yoshinori Matsuyama | Slowly releasing implement for chlorine dioxide gas |
JP2012147852A (en) * | 2011-01-17 | 2012-08-09 | Safe Section Inc | Chlorine dioxide controlled releasing agent, and chlorine dioxide controlled releasing agent contained in container |
CN102388919A (en) * | 2011-10-17 | 2012-03-28 | 华中农业大学 | Soil composite disinfectant and using method thereof |
JP2014025064A (en) * | 2012-07-24 | 2014-02-06 | Hao-Chang Yin | Chlorine dioxide gel and method for manufacturing the same |
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