JPH02284646A - Disoxidant - Google Patents

Disoxidant

Info

Publication number
JPH02284646A
JPH02284646A JP1103347A JP10334789A JPH02284646A JP H02284646 A JPH02284646 A JP H02284646A JP 1103347 A JP1103347 A JP 1103347A JP 10334789 A JP10334789 A JP 10334789A JP H02284646 A JPH02284646 A JP H02284646A
Authority
JP
Japan
Prior art keywords
oxygen
glycerin
water
oxygen scavenger
alkaline substance
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
Application number
JP1103347A
Other languages
Japanese (ja)
Other versions
JP2943156B2 (en
Inventor
Yasuo Sugihara
杉原 康夫
Takashi Kashiba
隆史 加柴
Hidetoshi Hatakeyama
秀利 畠山
Toshio Komatsu
小松 俊夫
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.)
Mitsubishi Gas Chemical Co Inc
Original Assignee
Mitsubishi Gas Chemical Co Inc
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 Mitsubishi Gas Chemical Co Inc filed Critical Mitsubishi Gas Chemical Co Inc
Priority to JP10334789A priority Critical patent/JP2943156B2/en
Priority to KR1019900002680A priority patent/KR930001255B1/en
Priority to CA002013803A priority patent/CA2013803C/en
Priority to US07/510,838 priority patent/US5180518A/en
Priority to EP90107340A priority patent/EP0394822B1/en
Priority to ES90107340T priority patent/ES2056288T3/en
Priority to DE69010550T priority patent/DE69010550T2/en
Publication of JPH02284646A publication Critical patent/JPH02284646A/en
Application granted granted Critical
Publication of JP2943156B2 publication Critical patent/JP2943156B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

PURPOSE:To obtain a disoxidant not detectable with a metal detector by blending glycerol with an alkaline substance. CONSTITUTION:A disoxidant is composed of glycerol and an alkaline substance such as NaOH or KOH. Water and/or a compd. (e.g. halide or sulfate) of a transition metal such as iron, e.g. ferrous chloride or ferrous sulfate or a slightly water soluble solid such as activated carbon or zeolite is further added as required. Since the highly hygroscopic glycerol is used as a base and iron powder is not used, a metal detector for checking the mixing of packed food with foreign matter can be worked without hindrance.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は脱酸素剤に関する。さらに詳I〜くけ、グリセ
リンを主剤志する新規な脱酸素剤に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an oxygen scavenger. In more detail, the present invention relates to a novel oxygen scavenger whose main ingredient is glycerin.

なお、本明細書で1脱酸素剤」とは主として[脱酸素作
用を有する組成物] (脱酸素剤組成物)の意味で用い
るが、「脱酸素作用を有する組成物の包装体」 (脱酸
素剤包装体)の意味で用いることもある。
In this specification, the term ``1 oxygen scavenger'' is mainly used to mean ``composition having an oxygen scavenging effect'' (oxygen scavenger composition), but it also refers to a ``package of a composition having an oxygen scavenging effect'' (oxygen scavenger composition). It is also sometimes used to mean an oxygen agent package.

〔従来の技術〕[Conventional technology]

食品等の保存技術として脱酸素剤を用いるものがあり、
これはガスバリヤ−性の密封袋または密閉容器(以下、
単に密封容器、または容器ということがある。)内に食
品等吉脱酸素剤^を存在させ密封系内を実質的に無酸素
状態とすることにより食品等の酸化および細菌や黴の生
育増殖等を抑えるものであり、広範な食品等の保存に用
いられている。
Oxygen absorbers are used as a preservation technique for foods, etc.
This is a gas-barrier sealed bag or container (hereinafter referred to as
Sometimes simply called a sealed container or container. ) The presence of food oxygen scavenger^ in the sealed system makes the sealed system virtually oxygen-free, thereby suppressing the oxidation of foods, etc. and the growth and proliferation of bacteria and mold. Used for preservation.

従来から脱酸素剤としては、その酸素吸収能力、取扱易
さ、安全性、コスト等の理由によって、鉄粉を主剤とす
るものが用いられてきた。
Conventionally, oxygen scavengers based on iron powder have been used for reasons such as their oxygen absorption ability, ease of handling, safety, and cost.

ところで、たとえば包装食品の場合、食品を包装袋に密
封後、異物混入をチエツクする為に金属検出器にかける
ことが行われている。
By the way, in the case of packaged foods, for example, after the food is sealed in a packaging bag, it is passed through a metal detector to check for foreign matter contamination.

しかしながら、鉄粉を主剤とする脱酸素剤は、当然この
金属検出器に検知される為、脱酸素剤を同封した包装食
品等には金属検出器が適用できなかった。
However, since oxygen absorbers based on iron powder are naturally detected by metal detectors, metal detectors cannot be applied to packaged foods that contain oxygen absorbers.

[発明が解決しようとする課題] 本発明の課題は、上記従来技術の問題点に鑑み、脱酸素
剤を金属検出器にかけても検知されないものとすること
である。
[Problems to be Solved by the Invention] In view of the problems of the prior art described above, an object of the present invention is to provide an oxygen scavenger that will not be detected even when applied to a metal detector.

〔課題を解決するための手段〕[Means to solve the problem]

上記の課題を解決する手段は、脱酸素剤をグリセリンと
アルカリ性物質からなる組成物としたことである。
A means for solving the above problems is to use a composition of glycerin and an alkaline substance as an oxygen scavenger.

解決手段の態様としては、(1)グリセリンとアルカリ
性物質からなる脱酸素剤、(2)グリセリン、アルカリ
性物質および水からなる脱酸素剤、(3)グリセリン、
アルカリ性物質および遷移金属化合物からなる脱酸素剤
、(4)グリセリン、アルカリ性物質、遷移金属化合物
および水からなる脱酸素剤、(5)グリセリン、アルカ
リ性物質および水難溶性固体からなる脱酸素剤、(6)
グリセリン、アルカリ性物質、水難溶性固体および水か
らなる脱酸素剤、(7)グリセリン、アルカリ性物質、
遷移金属化合物および水難溶性固体からなる脱酸素剤、
(8)グリセリン、アルカリ性物質、遷移金属化合物、
水難溶性固体および水からなる脱酸素剤が挙げられる。
Embodiments of the solution include (1) an oxygen scavenger made of glycerin and an alkaline substance, (2) an oxygen scavenger made of glycerin, an alkaline substance, and water, (3) glycerin,
Oxygen scavenger consisting of an alkaline substance and a transition metal compound, (4) Oxygen scavenger consisting of glycerin, an alkaline substance, transition metal compound and water, (5) Oxygen scavenger consisting of glycerin, an alkaline substance and a poorly water-soluble solid, (6) )
Glycerin, an alkaline substance, an oxygen scavenger consisting of a poorly water-soluble solid and water, (7) glycerin, an alkaline substance,
Oxygen scavenger consisting of a transition metal compound and a poorly water-soluble solid;
(8) Glycerin, alkaline substances, transition metal compounds,
Examples include oxygen scavengers consisting of poorly water-soluble solids and water.

なお、前記の解決手段において、グリセリンは通常市販
されているものでよく、水等の不純物が含まれていても
良い。
In the above-mentioned solution, the glycerin may be a commercially available glycerin, and may contain impurities such as water.

また、アルカリ性物質としては、水と作用してまたは水
に溶解してアルカリ性を呈する物質であり、アルカリ金
属又はアルカリ土類金属の水酸化物、炭酸塩、炭酸水素
塩、第三リン酸塩、第ニリン酸塩等が好ましく、アルカ
リ金属、アルカリ土類金属の水酸化物等が特に好ましい
。具体的には例えば、水酸化ナトリウム、炭酸ナトリウ
ム、炭酸水素ナトリウム、第三リン酸すl・リウム、第
ニリン酸ナトリウム、水酸化カリウム、炭酸カリウム、
炭酸水素カリウム、第三リン酸カリウム、第ニリン酸カ
リウム、水酸化カルシウム、水酸化マグネシウム等が好
ましい。これらの中でも水酸化ナトリウム、水酸化カリ
ウム、水酸化カルシウム等が特に好ましい。アルカリ性
物質は一種または二種以上の併用で用いることができる
。グリセリンに対するアルカリ性物質の混合量はグリセ
リン1(10)部(重量部、以下、同じ。)に対し10
部以上が好ましく、30−1.(10)0部が更に好ま
しい。アルカリ性物質の混合量が上記範囲より少ない場
合、組成物としての酸素吸収量が小さくなるので好まし
くなく、またアルカリ性物質の混合量が上記範囲より多
くなると、単位重量当たりの酸素吸収量が小ざくなるの
で組成物を包装する包材を大きくする必要があり、食品
包装体への装填面での不備が生じるとともに、外観面で
も好ましくない。
In addition, alkaline substances include substances that exhibit alkalinity by acting with or dissolving in water, such as hydroxides, carbonates, hydrogen carbonates, and tertiary phosphates of alkali metals or alkaline earth metals. Diphosphates and the like are preferred, and alkali metal and alkaline earth metal hydroxides are particularly preferred. Specifically, for example, sodium hydroxide, sodium carbonate, sodium hydrogen carbonate, sulfur and lithium triphosphate, sodium diphosphate, potassium hydroxide, potassium carbonate,
Potassium hydrogen carbonate, potassium triphosphate, potassium diphosphate, calcium hydroxide, magnesium hydroxide, and the like are preferred. Among these, sodium hydroxide, potassium hydroxide, calcium hydroxide, etc. are particularly preferred. The alkaline substances can be used alone or in combination of two or more. The amount of alkaline substance mixed with glycerin is 1 (10) parts (by weight, the same hereinafter) of glycerin.
Part or more is preferable, and 30-1. (10) 0 parts is more preferable. If the amount of the alkaline substance mixed is less than the above range, the amount of oxygen absorbed by the composition will be unfavorable, and if the amount of the alkaline substance mixed is more than the above range, the amount of oxygen absorbed per unit weight will be small. Therefore, it is necessary to increase the size of the packaging material used to package the composition, which leads to problems in loading the food package and is also unfavorable in terms of appearance.

遷移金属化合物としては、遷移金属のハロゲン化物、硫
酸塩、硝酸塩、リン酸塩、炭酸塩、有機酸塩、酸化物、
水酸化物、その他の複塩、キレト化合物等が挙げられる
。遷移金属きしては、鉄、コバルト、ニッケル、銅、亜
鉛、マンガン等が用いられ、銅、鉄、マンガン等が好ま
しく、安全性の面を考慮すると鉄が最も好ましい。最も
好ましい遷移金属化合物の具体例として、塩化第一鉄、
塩化第二鉄、硫酸第一鉄、硫酸第二鉄、水酸化第一鉄、
水酸化第二鉄、クエン酸鉄、酒石酸第一鉄、酒石酸第二
鉄等の無機または有機鉄化合物等を挙げることができる
。これらの遷移金属化合物は必要に応じて一種または二
種以上併用して添加されるもので、本発明の組成物の触
媒として働き、その配合量はグリセリン1(10)部に
対し、1部以上が好ましく、5部以上が特に好ましい。
Examples of transition metal compounds include transition metal halides, sulfates, nitrates, phosphates, carbonates, organic acid salts, oxides,
Examples include hydroxides, other double salts, and chelate compounds. As the transition metal, iron, cobalt, nickel, copper, zinc, manganese, etc. are used, and copper, iron, manganese, etc. are preferable, and iron is most preferable from the viewpoint of safety. Specific examples of the most preferred transition metal compounds include ferrous chloride,
Ferric chloride, ferrous sulfate, ferric sulfate, ferrous hydroxide,
Examples include inorganic or organic iron compounds such as ferric hydroxide, iron citrate, ferrous tartrate, and ferric tartrate. These transition metal compounds are added singly or in combination of two or more as necessary, and act as a catalyst for the composition of the present invention, and the amount of the transition metal compound is 1 part or more per 1 (10) parts of glycerin. is preferred, and 5 parts or more is particularly preferred.

水難溶性固体とは、水に不溶または難溶性の固体物質で
あり、具体的には、たとえば、活性炭、ゼオライト、パ
ーライト、珪藻上、活性白土、シリカ、カオリン、タル
ク、ベントカイト、活性アルミナ、石膏、シリカアル−
す、ケイ酸カルシウム、酸化マグネシウム、黒鉛、カー
ボンブラック、水酸化アルミニウム、酸化鉄等の粉末ま
たは粒状物が挙げられる。水難溶性固体は一種または二
種以上の併用で用いられる。水難溶性固体を配合するこ
とにより、酸素吸収速度または酸素吸収量の増加、組成
物の取り扱いを簡便にすることができる。また、水難溶
性固体の配合により組成物中の液状成分の酸素との接触
面積を大きくすることができる。水難溶性固体の配合量
は他成分との関係で適宜選択され、特に限定されないが
グリセリン1(10)部に対して0.1〜10.(10
)0部が好ましく、1〜i、 ooo部が特に好ましい
Slightly water-soluble solids are solid substances that are insoluble or sparingly soluble in water, and specifically include activated carbon, zeolite, perlite, diatomite, activated clay, silica, kaolin, talc, benthite, activated alumina, and gypsum. , silica al-
Examples include powders or granules of calcium silicate, magnesium oxide, graphite, carbon black, aluminum hydroxide, iron oxide, and the like. The poorly water-soluble solids may be used alone or in combination of two or more. By incorporating a poorly water-soluble solid, it is possible to increase the oxygen absorption rate or the amount of oxygen absorption, and to simplify the handling of the composition. Furthermore, by incorporating a poorly water-soluble solid, the contact area of the liquid component in the composition with oxygen can be increased. The amount of the poorly water-soluble solid to be blended is appropriately selected in relation to other components, and is not particularly limited, but is 0.1 to 10.0 parts per 1 (10) parts of glycerin. (10
) 0 parts are preferred, and 1 to i, ooo parts are particularly preferred.

本発明において上述した各成分の混合方法は特に制限は
ないが、成分が液と粉末との場合は各成分を均一に混合
できる方法ならいずれもよく、成分に粒状物を用いる場
合には、たとえば粒状物に液を含浸後粉分をまぶす様に
添加する方法等を採用することができる。前記各成分は
通常通気性包材に収容され、包装体とされる。その包装
方法としてはたとえば各成分を混合後、バッキングマシ
ンによって通気性包装材料の周縁部の熱シールによって
封じられた小袋に包み、脱酸素剤包装体とすることがで
きる。
In the present invention, there are no particular restrictions on the method of mixing the above-mentioned components, but if the components are liquid and powder, any method that can uniformly mix each component may be used, and if granules are used as the component, for example, A method may be adopted in which the liquid is impregnated into the granular material and then the powder is added so as to be sprinkled thereon. Each of the above components is usually housed in an air-permeable packaging material to form a package. As for the packaging method, for example, after mixing each component, it can be wrapped in a pouch sealed by heat-sealing the periphery of an air-permeable packaging material using a backing machine to form an oxygen absorber package.

この脱酸素剤包装体は、食品等とともに非通気性の包材
に収納し密封する、あるいは食品等とともに気密容器に
収容し密閉するなどの方法で食品等の保存に供すること
ができる。
This oxygen absorber package can be used to preserve foods, etc. by storing the oxygen absorber package together with foods, etc. in an air-impermeable packaging material and sealing it, or by storing it together with foods, etc. in an airtight container and sealing it.

〔作用〕[Effect]

本発明の脱酸素剤はその組成物中に水を入れない場合に
は、比較的水分の多い食品に適用し、食品より蒸散する
水分を組成物内に取り入れて酸素を吸収するタイプにす
ることができる。グリセリンは極めて吸湿性が強い為、
水分蒸散性の大きい雰囲気では良好な脱酸素機能を果た
す。この場合食品と共に密封するまでの取扱性が良いと
の長所がある。また、組成物中に水を入れれば、食品の
含水率には関係なく脱酸素する脱酸素剤とすることがで
きる。
When the oxygen absorber of the present invention does not contain water in its composition, it can be applied to foods with a relatively high moisture content, and the oxygen absorber of the present invention can be of a type that absorbs oxygen by incorporating moisture that evaporates from the food into the composition. I can do it. Glycerin is extremely hygroscopic, so
It has a good deoxidizing function in an atmosphere with high water evaporation. In this case, the advantage is that it is easy to handle until it is sealed together with food. Furthermore, if water is added to the composition, it can be used as an oxygen absorber that removes oxygen regardless of the water content of the food.

〔実施例〕〔Example〕

実施例1〜8 第1表に示す脱酸素剤各成分を混合した後、紙と有孔ポ
リエチレンをラミネートした包材を用いて作った小袋(
縦50mm、横80mm)に収納し、脱酸素剤包装体と
した。この脱酸素剤包装体を空気1゜(10)0m1.
とともに、ポリ塩化ビニリデンコートした延伸ナイロン
とポリエチレンをラミネートした袋に入れ、密封後、2
5℃の雰囲気に数百した。
Examples 1 to 8 After mixing the oxygen scavenger components shown in Table 1, a small bag (
50 mm long and 80 mm wide) to form an oxygen absorber package. This oxygen absorber package was heated to 1° (10) ml of air.
Then, put it in a bag made of polyvinylidene-coated stretched nylon and polyethylene, and after sealing it,
Several hundred people were placed in an atmosphere of 5℃.

6日後袋内の酸素濃度を測定し酸素吸収量を求めた結果
は第1表のとおりであった。
After 6 days, the oxygen concentration in the bag was measured and the amount of oxygen absorbed was determined. The results are shown in Table 1.

第1表(つづき) なお、実施例1.3.5および7については水を含浸さ
せた脱脂綿を一緒に密封し、相対湿度1(10)%下で
実施した。
Table 1 (Continued) For Examples 1.3.5 and 7, water-impregnated absorbent cotton was sealed together and the tests were carried out at a relative humidity of 1 (10)%.

実施例9 グリセリン2g、水酸化カルシウム2g、塩化第一鉄0
,4g、シリカ粉末1.2g、活性炭0.4gおよび水
1゜2gを混合して脱酸素剤として用いる以外は実施例
1と同様に操作した。
Example 9 Glycerin 2g, calcium hydroxide 2g, ferrous chloride 0
, 1.2 g of silica powder, 0.4 g of activated carbon, and 1.2 g of water were mixed and used as an oxygen scavenger.

2日後、袋内の酸素濃度を測定したところ酸素濃度は0
.1%以下であった。この時の酸素吸収量は206mn
であった。
Two days later, when I measured the oxygen concentration inside the bag, it was 0.
.. It was less than 1%. The amount of oxygen absorbed at this time is 206mn
Met.

実施例10 グリセリン2g、水酸化カルシウム3.4g、塩化マン
ガン0.6g、シリカ粉末2.6gおよび水2gを混合
して脱酸素剤として用いる以外は実施例1と同様に操作
した。
Example 10 The same procedure as in Example 1 was carried out except that 2 g of glycerin, 3.4 g of calcium hydroxide, 0.6 g of manganese chloride, 2.6 g of silica powder, and 2 g of water were mixed and used as an oxygen scavenger.

2日後、袋内の酸素濃度を測定したところ酸素濃度は0
.1%以下であった。この時の酸素吸収量は206rr
L1.であった。
Two days later, when I measured the oxygen concentration inside the bag, it was 0.
.. It was less than 1%. The amount of oxygen absorbed at this time was 206rr
L1. Met.

実施例11 グリセリン2g、水酸化カルシウム3.4g、硫酸銅0
、6g、活性炭2゜6gおよび水3.4gを混合して脱
酸素剤として用いる以外は実施例1と同様に操作した。
Example 11 2 g of glycerin, 3.4 g of calcium hydroxide, 0 copper sulfate
, 2.6 g of activated carbon, and 3.4 g of water were mixed and used as an oxygen scavenger, but the same procedure as in Example 1 was carried out.

2日後、袋内の酸素濃度を測定したところ酸素濃度は0
.1%以下であった。この時の酸素吸収量は206dで
あった。
Two days later, when I measured the oxygen concentration inside the bag, it was 0.
.. It was less than 1%. The amount of oxygen absorbed at this time was 206 d.

実施例12 コクゾウの成虫4(10)匹を玄米1 kg中で1週間
飼育した後、成虫を取り除いた。残った玄米を40gず
つに分け、以下の試料に供した。
Example 12 Four (10) adult brown elephants were raised in 1 kg of brown rice for one week, and then the adults were removed. The remaining brown rice was divided into 40 g portions and used for the following samples.

試料の玄米40gと実施例9の脱酸素剤包装体とを、ポ
リ塩化ビニリデンコート延伸ナイロンとポリエチレンを
ラミネートしてなる袋に入れ袋内空気量が1,(10)
0mj2となるように密封した。同一検体を10個作製
し20℃恒温室内に保存した。20日間保存した後開封
し、そのまま25℃で室内に置いて試料玄米から羽化し
てくるコクゾウの数を記録j−だ。
40 g of brown rice as a sample and the oxygen absorber package of Example 9 were placed in a bag made by laminating polyvinylidene chloride coated stretched nylon and polyethylene, and the air volume in the bag was 1.(10).
It was sealed so that it was 0 mj2. Ten identical specimens were prepared and stored in a thermostatic chamber at 20°C. After storing it for 20 days, open it and leave it indoors at 25 degrees Celsius to record the number of brown elephants that emerge from the brown rice sample.

対照区として脱酸素剤包装体を袋に同封しない以外は上
記と全く同一の試験を実施した。この場合羽化してくる
コクゾウの数を1(10)%とした。
As a control, the same test as above was conducted except that the oxygen absorber package was not enclosed in the bag. In this case, the number of brown elephants emerging was set at 1 (10)%.

結果を第2表に示す。The results are shown in Table 2.

実施例13 15gの饅頭10個と、実施例11の脱酸素剤包装体と
を、ポリ塩化ビニリデンコート延伸ナイロンとポリエチ
レンをラミネートしてなる袋に入れ袋内空気量が]、、
(10)0m7!となるようにして20℃で密封保存し
た。11週間後、袋内酸素濃度、炭酸ガス濃度を測定し
、饅頭の性状を観察した。
Example 13 Ten 15g steamed buns and the oxygen absorber package of Example 11 were placed in a bag made of a laminate of polyvinylidene chloride coated stretched nylon and polyethylene, and the amount of air in the bag was...
(10)0m7! It was stored sealed at 20°C. After 11 weeks, the oxygen concentration and carbon dioxide concentration in the bag were measured, and the properties of the manju were observed.

対照区として脱酸素剤包装体を袋に同封しない以外は上
記と全く同一の試験を実施した。
As a control, the same test as above was conducted except that the oxygen absorber package was not enclosed in the bag.

結果を第3表に示す。The results are shown in Table 3.

〔発明の効果〕〔Effect of the invention〕

本発明の脱酸素剤は鉄粉を用いていないので、食品と共
に密封後、金属検出器にかけても検知することはない為
、食品の異物混入検査が可能である。更に、グリセリン
を主剤としている為、成分面の安全性は高く、反応中に
有毒ガスを出すこともない。
Since the oxygen scavenger of the present invention does not use iron powder, it will not be detected even if it is placed in a metal detector after being sealed together with food, making it possible to test food for foreign matter contamination. Furthermore, since it uses glycerin as its main ingredient, it is highly safe in terms of ingredients and does not emit toxic gases during the reaction.

手続補正書 平成1年6月6日Procedural amendment June 6, 1999

Claims (10)

【特許請求の範囲】[Claims] (1)グリセリンとアルカリ性物質からなる脱酸素剤。(1) Oxygen scavenger consisting of glycerin and alkaline substances. (2)グリセリン、アルカリ性物質および水からなる脱
酸素剤。
(2) An oxygen scavenger consisting of glycerin, an alkaline substance and water.
(3)グリセリン、アルカリ性物質および遷移金属化合
物からなる脱酸素剤。
(3) An oxygen scavenger consisting of glycerin, an alkaline substance, and a transition metal compound.
(4)グリセリン、アルカリ性物質、遷移金属化合物お
よび水からなる脱酸素剤。
(4) An oxygen scavenger consisting of glycerin, an alkaline substance, a transition metal compound, and water.
(5)グリセリン、アルカリ性物質および水難溶性固体
からなる脱酸素剤。
(5) An oxygen scavenger consisting of glycerin, an alkaline substance, and a poorly water-soluble solid.
(6)グリセリン、アルカリ性物質、水難溶性固体およ
び水からなる脱酸素剤。
(6) An oxygen scavenger consisting of glycerin, an alkaline substance, a poorly water-soluble solid, and water.
(7)グリセリン、アルカリ性物質、遷移金属化合物お
よび水難溶性固体からなる脱酸素剤。
(7) An oxygen scavenger consisting of glycerin, an alkaline substance, a transition metal compound, and a poorly water-soluble solid.
(8)グリセリン、アルカリ性物質、遷移金属化合物、
水難溶性固体および水からなる脱酸素剤。
(8) Glycerin, alkaline substances, transition metal compounds,
An oxygen scavenger consisting of a poorly water-soluble solid and water.
(9)請求項1〜8のいずれかに記載の脱酸素剤を通気
性包材に収納してなる脱酸素剤包装体。
(9) An oxygen absorber package comprising the oxygen absorber according to any one of claims 1 to 8 housed in an air-permeable packaging material.
(10)請求項9に記載の脱酸素剤包装体と食品とを非
通気性包材または気密容器に収納し密封または密閉して
なる、食品包装体。
(10) A food package obtained by storing the oxygen absorber package according to claim 9 and a food in an air-impermeable packaging material or an airtight container and sealing or sealing the package.
JP10334789A 1989-04-25 1989-04-25 Oxygen scavenger Expired - Lifetime JP2943156B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP10334789A JP2943156B2 (en) 1989-04-25 1989-04-25 Oxygen scavenger
KR1019900002680A KR930001255B1 (en) 1989-04-25 1990-02-28 Deoxidation agent
CA002013803A CA2013803C (en) 1989-04-25 1990-04-04 Oxygen absorbent
EP90107340A EP0394822B1 (en) 1989-04-25 1990-04-18 Oxygen absorbent
US07/510,838 US5180518A (en) 1989-04-25 1990-04-18 Oxygen absorbent
ES90107340T ES2056288T3 (en) 1989-04-25 1990-04-18 OXYGEN ABSORBENT.
DE69010550T DE69010550T2 (en) 1989-04-25 1990-04-18 Oxygen absorption.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10334789A JP2943156B2 (en) 1989-04-25 1989-04-25 Oxygen scavenger

Publications (2)

Publication Number Publication Date
JPH02284646A true JPH02284646A (en) 1990-11-22
JP2943156B2 JP2943156B2 (en) 1999-08-30

Family

ID=14351608

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10334789A Expired - Lifetime JP2943156B2 (en) 1989-04-25 1989-04-25 Oxygen scavenger

Country Status (1)

Country Link
JP (1) JP2943156B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04126591A (en) * 1990-09-14 1992-04-27 Heisei Riken Kk Deoxidizer and method for using same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04126591A (en) * 1990-09-14 1992-04-27 Heisei Riken Kk Deoxidizer and method for using same
JPH0671593B2 (en) * 1990-09-14 1994-09-14 平成理研株式会社 Oxygen absorber and method of using the same

Also Published As

Publication number Publication date
JP2943156B2 (en) 1999-08-30

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