JPS60260401A - Manufacture of ice containing ozone - Google Patents

Manufacture of ice containing ozone

Info

Publication number
JPS60260401A
JPS60260401A JP11104584A JP11104584A JPS60260401A JP S60260401 A JPS60260401 A JP S60260401A JP 11104584 A JP11104584 A JP 11104584A JP 11104584 A JP11104584 A JP 11104584A JP S60260401 A JPS60260401 A JP S60260401A
Authority
JP
Japan
Prior art keywords
ozone
water
ice
contg
oxyacid
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
Application number
JP11104584A
Other languages
Japanese (ja)
Inventor
Seitaro Iki
伊木 誠太郎
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
KANKYO HOZEN KAIHATSU KK
Original Assignee
KANKYO HOZEN KAIHATSU KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by KANKYO HOZEN KAIHATSU KK filed Critical KANKYO HOZEN KAIHATSU KK
Priority to JP11104584A priority Critical patent/JPS60260401A/en
Publication of JPS60260401A publication Critical patent/JPS60260401A/en
Pending legal-status Critical Current

Links

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  • Catalysts (AREA)
  • Oxygen, Ozone, And Oxides In General (AREA)

Abstract

PURPOSE:To manufacture ice contg. ozone by cooling water contg. dissolved ozone and adding a ferric compound of oxyacid in vegetable acid or oxyacid produced by the oxidation of saccharides as a catalyst immediately before freezing. CONSTITUTION:About 5ppm ozone is dissolved in water and this water is cooled. The ferric compound of oxyacid in vegetable acid or oxyacid produced by the oxidation of saccharides, e.g., ferric gluconate or ferric glycolate is added to the water as a catalyst by a small amount immediately before freezing, and the water is frozen to manufacture ice contg. ozone. When caught fishes are preserved with the ice contg. ozone on the sea, the ice maintains the freshness for a longer time than ice contg. ozone manufactured without adding the catalyst.

Description

【発明の詳細な説明】 「産業上の利用分野」 本発明はオゾン氷の製造法に関するものである。[Detailed description of the invention] "Industrial application field" The present invention relates to a method for producing ozone ice.

「従来の技術」 食品の鮮度保持を目的として、本発明者は先にオゾンを
溶解した水を冷却し氷結させることに工って製造するオ
ゾン氷を開発した。
"Prior Art" For the purpose of preserving the freshness of foods, the present inventor developed ozone ice, which is produced by cooling and freezing water in which ozone has been dissolved.

しかし、斯かるオゾン氷は食品の鮮度保持については確
かに効果的ではあるが、その鮮度保持期間が意外に短か
いという問題点があった。
However, although such ozone ice is certainly effective in preserving the freshness of food, it has a problem in that its freshness preservation period is surprisingly short.

「発明が解決しようとする問題点」 そこで本発明者は斯かる問題点を解決すべく更に研究し
、実験を重ねた結果、オゾンを溶解した水を冷却してオ
ゾン氷を製造するに際し、その氷。
"Problems to be Solved by the Invention" Therefore, the inventor of the present invention conducted further research and conducted repeated experiments to solve these problems. ice.

結電前に植物酸中のオキシ酸又は糖類の酸化によるオキ
シ酸の第二、鉄化合物を触媒として添加することによっ
て、前記問題点が解決することを発見した。
It has been discovered that the above-mentioned problems can be solved by adding, as a catalyst, an oxyacid in a vegetable acid or an oxyacid secondary to oxidation of sugars, and an iron compound before electricity formation.

尚、実験中において前記以外の触媒、例えば無機の鉄イ
オンを用いて実験を行ってみたが、この場合にはオゾン
の酸化反応速度も増す反面、オゾンの自己分解反応も促
進され、それ程効果的ではないことが分つ、た。さらに
またこの場合には反応 □終了後水酸化第二鉄の析出が
起こシ、商品価値を著しく減することも分った。
During the experiment, we tried using a catalyst other than the above, for example, inorganic iron ions, but in this case, the ozone oxidation reaction rate increased, but the ozone self-decomposition reaction was also accelerated, so it was not as effective. It turns out that's not the case. Furthermore, it has been found that in this case, precipitation of ferric hydroxide occurs after the reaction is completed, which significantly reduces the commercial value.

「問題点を解決するための手段」 本発明に係るオゾン氷の製造法は、前記の通電、オゾン
を溶解した水を冷却し、その氷結直前に植物酸中のオキ
シ酸又は糖類の酸化によるオキシ酸の第二鉄化合物を触
媒として添加することを特徴とするものである。これに
よってオゾンの酸化反応速度が促進され、鮮度保持期間
が大幅に伸びるようになった。
"Means for Solving the Problems" The method for producing ozone ice according to the present invention includes the above-mentioned energization, cooling the water in which ozone has been dissolved, and immediately before freezing, oxidation of oxyacids or sugars in vegetable acids. This method is characterized by adding a ferric acid compound as a catalyst. This accelerates the oxidation reaction rate of ozone and significantly extends the freshness period.

「実施例」 次に本発明の実施例について説明する。"Example" Next, examples of the present invention will be described.

オゾンを溶解した水(オゾン水)を冷却し、氷結直前に
グルコン酸第二鉄又はグリコール酸第二鉄を触媒として
少量添加し、氷結させてオゾン水を製造した。
Ozone water was produced by cooling water in which ozone was dissolved (ozone water), adding a small amount of ferric gluconate or ferric glycolate as a catalyst just before freezing, and freezing the water.

このオゾン水を冷蔵庫に入れたままにしておき、1ケ月
後に取り出して室温で溶解させ、溶解したオゾン水を検
昂した結果は次の通りであった。
This ozonated water was left in the refrigerator, and after one month, it was taken out and dissolved at room temperature. The dissolved ozonated water was tested and the results were as follows.

A)5ppmのオゾンを溶解したオゾン水にグルコン酸
第二鉄を添加した場合の枯草菌(有芽胞菌)の滅菌に要
する時間 B)2ppmのオゾンを溶解したオゾン水にグルコン酸
第二鉄を添加した場合の犬鳴菌の滅菌に要する時間 C)5ppmのオゾンを溶解したオゾン水にグリコール
酸第二鉄を添加した場合のメチルオレンジの水溶液を1
40に脱色するに要する時間尚上記の色素脱色試験は特
許第412776号に準拠したものであシ、色素に対す
る脱色作用はとシもなおさず滅菌作用を示すものである
A) Time required to sterilize Bacillus subtilis (spore-forming bacteria) when ferric gluconate is added to ozonated water with 5 ppm of ozone dissolved B) Ferric gluconate is added to ozonated water with 2 ppm of ozone dissolved Time required for sterilization of Inunaki bacteria when added C) An aqueous solution of methyl orange when ferric glycolate is added to ozonated water in which 5 ppm of ozone is dissolved.
Time required for decolorization to 40% The above dye decolorization test was based on Japanese Patent No. 412776, and shows a sterilization effect without any decolorization effect on the dye.

また、更に本発明によって製造したオゾン水を海上で捕
獲した魚類の保存に使用した時、触媒を添加しないオゾ
ン水を用いた場合よシも更に鮮度が長もちし、実験の結
果本発明によって製造したオゾン水の有効期間は約1ケ
月程度あることが判明した。
Furthermore, when the ozonated water produced according to the present invention was used to preserve fish caught at sea, the freshness lasted longer than when ozonated water without the addition of a catalyst was used, as a result of experiments. It was found that ozonated water has an effective period of about one month.

また本発明において触媒として用いるグルコン酸第二鉄
等は、水溶液中で三価の鉄イオンを持ち、しかも鉄イオ
ンが化学的に隠蔽されて、−の変化等では容易に沈澱が
起こらない性質を有しておシ、且つまた味に変化を与え
ないものである。それ故商品の品質は全く損なわれるこ
ともないものである。
Furthermore, the ferric gluconate used as a catalyst in the present invention has trivalent iron ions in an aqueous solution, and the iron ions are chemically hidden and do not easily precipitate due to changes in -. It is easy to use and does not change the taste. Therefore, the quality of the product is not compromised at all.

「発明の効果」 本発明によれば前記したとお夛、有機オキシ酸の第二鉄
化合物を触媒として添加することによってオゾンの酸化
反応速度が促進され、もってオゾン水の鮮度保持期間を
大幅に引き伸ばすことができるようになった。
"Effects of the Invention" According to the present invention, as mentioned above, the oxidation reaction rate of ozone is accelerated by adding the ferric compound of organic oxyacid as a catalyst, thereby significantly extending the freshness retention period of ozonated water. Now I can do it.

Claims (1)

【特許請求の範囲】[Claims] オゾンを溶解した水を冷却し、その氷結直前に植物酸中
のオキシ酸又は糖類の酸化によるオキシ酸の第二鉄化合
物を触媒として添加することを特徴とするオゾン氷の製
造法。
1. A method for producing ozone ice, which comprises cooling water in which ozone is dissolved, and adding, as a catalyst, a ferric compound of an oxyacid produced by oxidizing an oxyacid or sugar in a vegetable acid just before freezing.
JP11104584A 1984-06-01 1984-06-01 Manufacture of ice containing ozone Pending JPS60260401A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11104584A JPS60260401A (en) 1984-06-01 1984-06-01 Manufacture of ice containing ozone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11104584A JPS60260401A (en) 1984-06-01 1984-06-01 Manufacture of ice containing ozone

Publications (1)

Publication Number Publication Date
JPS60260401A true JPS60260401A (en) 1985-12-23

Family

ID=14551011

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11104584A Pending JPS60260401A (en) 1984-06-01 1984-06-01 Manufacture of ice containing ozone

Country Status (1)

Country Link
JP (1) JPS60260401A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0380962A2 (en) * 1989-02-01 1990-08-08 Seymour Siegel Method and apparatus for obtaining ozone saturated water
US7846408B1 (en) 2006-11-21 2010-12-07 Cox Jr Henry Wilmore Compositions, methods, and systems for managing total sulfide
US8480924B1 (en) 2004-02-02 2013-07-09 Henry Wilmore Cox, Jr. Compositions, methods, and systems for reducing contamination
US8609926B1 (en) 2006-11-21 2013-12-17 Henry Wilmore Cox, Jr. Methods for managing sulfide in wastewater systems
US9023780B2 (en) 2010-04-14 2015-05-05 Ecolab Usa Inc. Ferric hydroxycarboxylate as a builder

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0380962A2 (en) * 1989-02-01 1990-08-08 Seymour Siegel Method and apparatus for obtaining ozone saturated water
US8480924B1 (en) 2004-02-02 2013-07-09 Henry Wilmore Cox, Jr. Compositions, methods, and systems for reducing contamination
US8858806B1 (en) 2004-02-02 2014-10-14 Henry Wilmore Cox, Jr. Method for reducing contamination
US7846408B1 (en) 2006-11-21 2010-12-07 Cox Jr Henry Wilmore Compositions, methods, and systems for managing total sulfide
US8609926B1 (en) 2006-11-21 2013-12-17 Henry Wilmore Cox, Jr. Methods for managing sulfide in wastewater systems
US9067812B1 (en) 2006-11-21 2015-06-30 Henry Wilmore Cox, Jr. Methods for managing sulfide in wastewater systems
US9023780B2 (en) 2010-04-14 2015-05-05 Ecolab Usa Inc. Ferric hydroxycarboxylate as a builder

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