JPH02284645A - Disoxidant - Google Patents

Disoxidant

Info

Publication number
JPH02284645A
JPH02284645A JP1103346A JP10334689A JPH02284645A JP H02284645 A JPH02284645 A JP H02284645A JP 1103346 A JP1103346 A JP 1103346A JP 10334689 A JP10334689 A JP 10334689A JP H02284645 A JPH02284645 A JP H02284645A
Authority
JP
Japan
Prior art keywords
glycol
oxygen
transition metal
water
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
JP1103346A
Other languages
Japanese (ja)
Other versions
JP2943155B2 (en
Inventor
Yasuo Sugihara
杉原 康夫
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 JP10334689A priority Critical patent/JP2943155B2/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 DE69010550T priority patent/DE69010550T2/en
Priority to ES90107340T priority patent/ES2056288T3/en
Publication of JPH02284645A publication Critical patent/JPH02284645A/en
Application granted granted Critical
Publication of JP2943155B2 publication Critical patent/JP2943155B2/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 1,2-glycol with an alkaline substance and a compd. of a transition metal. CONSTITUTION:A disoxidant is composed of 1,2-glycol such as ethylene glycol or propylene glycol, an alkaline substance such as NaOH or KOH and a compd. (e.g. halide or sulfate) of a transition metal such as iron or cobalt. Water and/or a slightly water soluble solid such as activated carbon or zeolite is further added as required. Since the highly hygroscopic glycol is used as a base and iron powder is not used, a metal detector for checking mixing 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。さらに詳しくは、1.2−
グリコールを主剤とする新規な脱酸素剤に関する。なお
、本明細書で「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。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an oxygen scavenger. For more details, see 1.2-
This invention relates to a novel oxygen absorber containing glycol as a main ingredient. In this specification, the term "oxygen scavenger" is mainly used to mean a "composition that has an oxygen scavenging effect" (oxygen scavenger composition), but it also refers to a "package of a composition that has 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]

食品等の保存技術上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
品等と脱酸素剤と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。
Some food preservation techniques use oxygen absorbers.
This is a gas-barrier sealed bag or container (hereinafter referred to as
Sometimes simply called a sealed container or container. ) By placing food, etc. and an oxygen scavenger inside the sealed system to create a substantially oxygen-free condition, it suppresses 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〕[Problem to be solved by the invention]

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。
In view of the above-mentioned problems of the prior art, 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1−92グリ
コール、アルカリ性物質および遷移金属化合物からなる
組成物としたことである。
A means for solving the above problems is to use a composition of 1-92 glycol, an alkaline substance, and a transition metal compound as an oxygen scavenger.

解決手段の態様としては、(1)1.2−グリコール、
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
、(20,2〜グリコール、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、(3)1.2グリコ
ール、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、(4)1.2−グリコール、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。
Aspects of the solution include (1) 1,2-glycol;
Oxygen scavenger consisting of an alkaline substance and a transition metal compound, (20,2-oxygen scavenger consisting of glycol, alkaline substance, transition metal compound, and water, (3) 1.2 glycol, alkaline substance, transition metal compound, and poorly water-soluble Oxygen scavengers made of solids, and (4) oxygen scavengers made of 1,2-glycol, alkaline substances, transition metal compounds, poorly water-soluble solids, and water.

なお、前記の解決手段において、1,2−グリコールは
通常市販されているものでよく、水等の不純物が含まれ
ていてもよく、混合物でもよい。1,2グリコールとし
ては、たとえばエチレングリコール、プロピレングリコ
ール等が好ましく、プロピレングリコールが特に好まし
い。
In the above solution, the 1,2-glycol may be a commercially available one, may contain impurities such as water, or may be a mixture. As the 1,2 glycol, for example, ethylene glycol, propylene glycol, etc. are preferable, and propylene glycol is particularly preferable.

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、炭酸すj・リ
ウム、炭酸水素ナトリウム、第三リン酸す)・リウム、
第リン酸すトリウム、水酸化カリウド、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すトリウム、水酸化カリ
ウム、水酸化カルシウド等が特に好ま(〜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。、1,2−グリコーに対するアルカリ性物質の混合
量は1.2−グリコール100部(重量部、以下、同じ
。)に対し10部以上が好ましく、30〜1.000部
が更に好ましい。
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 bicarbonate, tribasic phosphate,
Sothorium phosphate, potassium hydroxide, potassium carbonate,
Potassium hydrogen carbonate, potassium triphosphate, potassium diphosphate, calcium hydroxide, magnesium hydroxide, and the like are preferred. Among these, thorium hydroxide, potassium hydroxide, calcium hydroxide, etc. are particularly preferable (...).Alkaline substances can be used alone or in combination of two or more types. The amount is preferably 10 parts or more, more preferably 30 to 1.000 parts, based on 100 parts (parts by weight, the same applies hereinafter) of 1.2-glycol.

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さくなるので組成
物を包装する包材が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。
If the amount of the alkaline substance mixed is less than the above range, the amount of oxygen absorbed by the composition will be small, which is undesirable.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. The packaging material for packaging the composition needs to be large, which causes problems in loading the food package and is also unfavorable in terms of appearance.

遷移金属化合物としでは−X 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。遷移金属としては、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(−<、安全性の面を考慮すると、鉄が最も好まL
7い。最も好ましい具体例として、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
ら遷移金属化合物は一種または二種以上併用I7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1.2−グリコール100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 the transition metal compound include -X transition metal halides, sulfates, nitrates, phosphates, carbonates, organic acid salts, oxides, 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 (-<, considering safety, iron is the most preferable).
7. Most preferred specific examples include ferrous chloride, ferric chloride, ferrous sulfate, ferric sulfate, ferrous hydroxide, ferric hydroxide, ferrous citrate, ferrous tartrate, and ferric tartrate. Examples include inorganic or organic iron compounds such as iron. These transition metal compounds are added singly or in combination of two or more and act as catalysts in the composition of the present invention, and the amount thereof is preferably 1 part or more per 100 parts of 1,2-glycol. Parts or more are 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、珪藻土、活性白土、シリカ、カオリン、タル
ク、ベントナイト、活性アルミナ、石膏、シリカアルミ
ナ、ケイ酸カルシウム、酸化マグネジウド、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。水難溶性固体は必要に応じて
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。
Slightly water-soluble solids are solid substances that are insoluble or sparingly soluble in water, and specifically include activated carbon, zeolite, perlite, diatomaceous earth, activated clay, silica, kaolin, talc, bentonite, activated alumina, gypsum, and silica. Examples include powders or granules of alumina, 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, if necessary. 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.

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100部に対して0.1〜10
.000部が好ましく、1〜1.000部が特に好まし
い。
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 parts per 100 parts of glycerin.
.. 000 parts is preferred, and 1 to 1.000 parts is 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、成分が液お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 or powder, any method that allows each component to be mixed uniformly may be used; 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。特にエチレングリコール、プロピレン
グリコール等の1.2グリコール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。
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. In particular, 1.2 glycols such as ethylene glycol and propylene glycol have extremely strong hygroscopic properties, and therefore perform a good deoxidizing function in an atmosphere with a high rate of water evaporation.

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
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1〜4 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500rn1.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、25℃の
雰囲気に放置した。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。
Examples 1 to 4 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 aired at 500rn1. At the same time, the bag was placed in a bag made by laminating polyvinylidene chloride-coated stretched nylon and polyethylene, and after being sealed, the bag was left in an atmosphere at 25°C. 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.

なお、実施例1および3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100%下で実施した。
Note that in Examples 1 and 3, absorbent cotton impregnated with water was sealed together and the tests were carried out at a relative humidity of 100%.

実施例5 プロピレングリコール5g1水酸化カルシウム5g1塩
化マンガン1g、活性炭5gおよび水5g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 5 The same procedure as in Example 1 was carried out except that 5 g of propylene glycol, 5 g of calcium hydroxide, 1 g of manganese chloride, 5 g of activated carbon, and 5 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LOW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 LOW.

実施例6 エチレングリコール5g1水酸化カルシウム5g、塩化
第一鉄1g、活性炭5gおよび水5g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 6 The same procedure as in Example 1 was carried out except that 5 g of ethylene glycol, 5 g of calcium hydroxide, 1 g of ferrous chloride, 5 g of activated carbon and 5 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103m1
.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 103 m1
.. Met.

実施例7 コクゾウの成虫400匹を玄米1kg中で1週間飼育し
た後、成虫を取り除いた。残った玄米を20gずつに分
け、以下の試料に供した。
Example 7 After raising 400 adult black elephants in 1 kg of brown rice for one week, the adults were removed. The remaining brown rice was divided into 20 g portions and used for the following samples.

試料の玄米20gと実施例5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ボリエヂレンを
ラミネートしてなる袋に入れ袋内空気量が500d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
ウの数を記録した。
20 g of brown rice as a sample and the oxygen scavenger package of Example 5 were placed in a bag made by laminating polyvinylidene chloride coated stretched nylon and polyethylene, and the bag was sealed so that the amount of air in the bag was 500 d. Ten identical specimens were prepared and stored in a thermostatic chamber at 20°C. After storing it for 20 days, it was opened and placed indoors at 25°C, and the number of brown elephants emerging from the sample brown rice was recorded.

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100%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 taken as 100%.

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

実施例8 ]、5gの饅頭5個と、実施例6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唐ポリエチレ
ンをラミネートしてなる袋に入れ袋内空気量が500m
Aとなるようにして20℃で密封保存した。1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 8], five 5g manju buns and the oxygen absorber package of Example 6 were placed in a bag made of polyvinylidene chloride coated stretched nylon-tang polyethylene laminated, and the air volume in the bag was 500 m
It was stored sealed at 20°C as shown in A. 1 week later,
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、■、2−グ
リコール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吉もない。
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. In addition, since it uses 2-glycol as its main ingredient, it is highly safe in terms of ingredients.
There is no possibility of releasing toxic gas during the reaction.

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

Claims (8)

【特許請求の範囲】[Claims] (1)1,2−グリコール、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。
(1) An oxygen scavenger consisting of 1,2-glycol, an alkaline substance and a transition metal compound.
(2)1,2−グリコール、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。
(2) An oxygen scavenger consisting of 1,2-glycol, an alkaline substance, a transition metal compound, and water.
(3)1,2−グリコール、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。
(3) An oxygen scavenger consisting of 1,2-glycol, an alkaline substance, a transition metal compound, and a poorly water-soluble solid.
(4)1,2−グリコール、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。
(4) An oxygen scavenger consisting of 1,2-glycol, an alkaline substance, a transition metal compound, a poorly water-soluble solid, and water.
(5)1,2−グリコールがエチレングリコールである
請求項1〜4のいずれかに記載の脱酸素剤。
(5) The oxygen scavenger according to any one of claims 1 to 4, wherein the 1,2-glycol is ethylene glycol.
(6)1,2−グリコールがプロピレングリコールであ
る請求項1〜4のいずれかに記載の脱酸素剤。
(6) The oxygen scavenger according to any one of claims 1 to 4, wherein the 1,2-glycol is propylene glycol.
(7)請求項1〜6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。
(7) An oxygen absorber package comprising the oxygen absorber according to any one of claims 1 to 6 housed in an air-permeable packaging material.
(8)請求項7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。
(8) A food package obtained by storing the oxygen absorber package according to claim 7 and a food in an air-impermeable packaging material or an airtight container and sealing or sealing the package.
JP10334689A 1989-04-25 1989-04-25 Oxygen scavenger Expired - Lifetime JP2943155B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP10334689A JP2943155B2 (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
DE69010550T DE69010550T2 (en) 1989-04-25 1990-04-18 Oxygen absorption.
ES90107340T ES2056288T3 (en) 1989-04-25 1990-04-18 OXYGEN ABSORBENT.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10334689A JP2943155B2 (en) 1989-04-25 1989-04-25 Oxygen scavenger

Publications (2)

Publication Number Publication Date
JPH02284645A true JPH02284645A (en) 1990-11-22
JP2943155B2 JP2943155B2 (en) 1999-08-30

Family

ID=14351578

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10334689A Expired - Lifetime JP2943155B2 (en) 1989-04-25 1989-04-25 Oxygen scavenger

Country Status (1)

Country Link
JP (1) JP2943155B2 (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
JP2943155B2 (en) 1999-08-30

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