JPH04190772A - Alcohol absorbent for packaged food - Google Patents

Alcohol absorbent for packaged food

Info

Publication number
JPH04190772A
JPH04190772A JP2326519A JP32651990A JPH04190772A JP H04190772 A JPH04190772 A JP H04190772A JP 2326519 A JP2326519 A JP 2326519A JP 32651990 A JP32651990 A JP 32651990A JP H04190772 A JPH04190772 A JP H04190772A
Authority
JP
Japan
Prior art keywords
alcohol
absorbent
days
weight
ethanol
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
JP2326519A
Other languages
Japanese (ja)
Inventor
Eiji Hashimoto
橋本 榮治
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Individual
Original Assignee
Individual
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Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP2326519A priority Critical patent/JPH04190772A/en
Publication of JPH04190772A publication Critical patent/JPH04190772A/en
Pending legal-status Critical Current

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  • Storage Of Fruits Or Vegetables (AREA)
  • Food Preservation Except Freezing, Refrigeration, And Drying (AREA)

Abstract

PURPOSE:To obtain the subject absorbent capable of quickly absorbing and removing residual alcohol, etc., in a packaging bag by combining a physical adsorptive reaction agent composed of a porous substance with a specific compound capable of forming an alcohol adduct. CONSTITUTION:The objective alcohol absorbent is composed of (A) a physical adsorptive reaction agent consisting of a porous substance such as zeolite or activated carbon and (B) a chemical absorptive reaction agent capable of forming an alcohol adduct and selected from a deliquescent inorganic salt (e.g. sodium chloride), an organic acid (e.g. adipic acid) and/or an organic acid salt (e.g. sodium adipate).

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、包装用袋内に封入する食品の殺菌・鮮度保持
を目的として殺菌用アルコール液を使用した場合に、包
装用袋内に残留するそのアルコール液や蒸散アルコール
ガス分を吸収するための包装食品のアルコール吸収剤に
関するものである。
[Detailed Description of the Invention] <Industrial Application Field> The present invention provides a method for eliminating residual alcohol in the packaging bag when a sterilizing alcohol solution is used for the purpose of sterilizing and preserving the freshness of food sealed in the packaging bag. This invention relates to an alcohol absorbent for packaged foods for absorbing alcohol liquid and evaporated alcohol gas.

〈従来の技術〉 従来より、水産加工食品をはじめ、生食品、半乾燥食品
、各種惣村、菓子類まで、殆どの包装食品には、その殺
菌・鮮度保持を目的として鮮度保持液を混和せしめたア
ルコール液が使用されている。
<Conventional technology> Traditionally, most packaged foods, including processed seafood foods, raw foods, semi-dried foods, various side dishes, and confectionery, have been mixed with a freshness-preserving liquid for the purpose of sterilizing and preserving freshness. Alcohol solution is used.

しかしながら、このような殺菌処理をすると、包装用袋
内にアルコール分やアルコール臭が残存し、食する際に
不快感を与えたり芳香の変香、賞味の変質などをきたす
弊害があった。
However, when such sterilization treatment is carried out, alcohol content and alcohol odor remain in the packaging bag, causing discomfort when eating, changing the aroma, and deteriorating the taste.

〈発明が解決しようとする課題〉 本発明はこの様な従来の不具合に鑑みてなされたもので
あり、包装用袋内に残留する殺菌用アルコール液や蒸散
アルコールガス分を速やかに吸収除去することが出来る
包装食品のアルコール吸収剤を提供せんとするものであ
る。
<Problems to be Solved by the Invention> The present invention has been made in view of these conventional problems, and it is an object of the present invention to promptly absorb and remove the sterilizing alcohol liquid and evaporated alcohol gas remaining in the packaging bag. The purpose of this invention is to provide an alcohol absorbent for packaged foods that can be used to absorb alcohol.

〈課題を解決するための手段〉 斯る目的を達成する本発明の包装食品のアルコール吸収
剤は、多孔質性物質からなる物理吸着反応剤と、化学吸
収反応剤としてのアルコール付加物生成可能な潮解性無
機塩、有機酸、有機酸塩から選ばれた1種もしくは2種
以上の成分とから成ることを特徴としたものである。
<Means for Solving the Problems> The alcohol absorbent for the packaged food of the present invention that achieves the above purpose comprises a physical adsorption reactant made of a porous substance and a chemical absorption reactant capable of producing an alcohol adduct. It is characterized by consisting of one or more components selected from deliquescent inorganic salts, organic acids, and organic acid salts.

〈実施例〉 以下、本発明の詳細な説明する。<Example> The present invention will be explained in detail below.

本発明で用いられる吸収剤原料のうち、物理吸着反応剤
としては、例えばゼオライト、セピオライト、バーミキ
ュライト、黄土、白土、カオリン。
Among the absorbent raw materials used in the present invention, physical adsorption reactants include, for example, zeolite, sepiolite, vermiculite, loess, white clay, and kaolin.

タルク、ベントナイト、パーライト、焼成又は乾燥ゼオ
ライト、珪藻土、大谷石、活性炭、シリカ。
Talc, bentonite, perlite, calcined or dried zeolite, diatomaceous earth, Oya stone, activated carbon, silica.

アルミナ、軽焼マグネシア、アルミナシリカ、シリカゲ
ル、シリカアルミナ、無水硫酸マグネシウム、合成ケイ
酸アルミニウム、焼石膏9等の多孔質性物質類を、また
化学吸収反応剤としてはアルコール付加物生成可能な、
例えば塩化ナトリウム。
Porous substances such as alumina, light calcined magnesia, alumina silica, silica gel, silica alumina, anhydrous magnesium sulfate, synthetic aluminum silicate, calcined gypsum 9, etc., and chemical absorption reactants capable of producing alcohol adducts,
For example, sodium chloride.

塩化カルシウム、塩化マグネシウム、塩化アルミニウム
、塩化鉄、亜塩素酸ナトリウム等の潮解性無機塩、或い
はクエン酸及びナトリウム塩、りんご酸及びナトリウム
塩、酒石酸及びカリウム塩。
Deliquescent inorganic salts such as calcium chloride, magnesium chloride, aluminum chloride, iron chloride, sodium chlorite, or citric acid and sodium salts, malic acid and sodium salts, tartaric acid and potassium salts.

フマール酸及びナトリウム塩、アジピン酸及びナトリウ
ム塩等の有機酸と有機酸塩とを混合したもの、などを挙
げることができる。
Examples include mixtures of organic acids and organic acid salts such as fumaric acid and sodium salts, adipic acid and sodium salts, and the like.

本発明に係る化学吸着反応剤としての有機酸及び有機酸
塩は、従来から知られている制菌乃至は殺菌作用による
食品の腐敗防止効果は勿論のこと、アルコール付加物の
生成に伴うアルコール吸収効果をも目的としたものであ
る。即ち、有機酸及び有機酸塩には、クエン酸のように
水溶性であるがエタノールに難溶性のものやフマール酸
のようにエタノールには可溶性であるが水に難溶性であ
るといった特性があり、この様な有機酸及び有機酸塩を
アルコール雰囲気中で使用することにより、食品のより
有効な殺菌・鮮度保持効果とアルコール吸収効果を発揮
させるものである。
The organic acids and organic acid salts as chemisorption reactants according to the present invention not only have the effect of preventing spoilage of food through the conventionally known bacteriostatic or bactericidal action, but also the ability to absorb alcohol due to the production of alcohol adducts. It is also intended for effectiveness. That is, organic acids and organic acid salts have characteristics such as those that are soluble in water but poorly soluble in ethanol, such as citric acid, and those that are soluble in ethanol but poorly soluble in water, such as fumaric acid. By using such organic acids and organic acid salts in an alcohol atmosphere, more effective sterilization and freshness preservation effects and alcohol absorption effects on foods can be exhibited.

そして、本発明に係るアルコール吸収剤は、紙や多孔性
プラスチックフィルム、或いは紙と多孔性プラスチック
フィルムとの積層体からなる通気性を有する袋体内に入
れて使用され、使用に際しては前記成分の微粉末、粗粉
末9粒状いづれでも使用可能であり、また各成分の単体
でも2種以上を混和したものでも使用可能である。
The alcohol absorbent according to the present invention is used in an air permeable bag made of paper, a porous plastic film, or a laminate of paper and a porous plastic film, and when used, the alcohol absorbent is used in a bag with air permeability made of paper, a porous plastic film, or a laminate of paper and a porous plastic film. It can be used in the form of powder or coarse powder, and each component can be used alone or in a mixture of two or more.

次に、本発明の好適実施例を記すが、本発明は以下の実
施例に限定されるものではない。
Next, preferred embodiments of the present invention will be described, but the present invention is not limited to the following embodiments.

実施例1゜ アルコール吸収剤としての物理吸着反応剤の性能を調べ
るために、焼石膏、亜硫酸カルシウム。
Example 1 In order to investigate the performance of the physical adsorption reactant as an alcohol absorbent, calcined gypsum and calcium sulfite were used.

粒状焼成ゼオライト、粒状セピオライト、微粉末セピオ
ライト、砂状ヤシガラ活性炭等の多孔質性物質を選択し
、2gづつを市販のヒートシール可能で通気性の良い撥
水性紙のバルブシートからなる吸収剤収納用袋体内に収
納せしめて、上記6種類のアルコール吸収剤を作成した
。他方、食品包装用袋として内容積的500ccのガス
バリアー性の高いプラスチックフィルム製袋(厚さ;6
0μmのKOPフィルム)を用い、その内に内容積的2
00ccのプラスチックトレーを入れ、このトレーの左
端部にエタノール(−級試薬、純度、 99.5%、比
重;約0.8)3ccを滴下したカット面を載せると共
に、上記作成したアルコール吸収剤をトレーの右端部に
両面テープで固定し、プラスチックフィルム製袋の開口
部をヒートシール密封した。この試験体を各2検体作成
し、常温(13℃〜17℃)での重量増加の経日変化を
測定し、エタノール吸収量の比較実験をした。その結果
を別紙の表1に示す。
Select a porous material such as granular calcined zeolite, granular sepiolite, finely powdered sepiolite, or sandy coconut shell activated carbon, and add 2 g each to a commercially available heat-sealable, breathable, water-repellent paper valve sheet for absorbent storage. The six types of alcohol absorbents mentioned above were prepared by storing them in bags. On the other hand, a plastic film bag with a high gas barrier property (thickness: 6
0μm KOP film), and the internal volume is 2.
A 00cc plastic tray was placed, and the cut surface on which 3cc of ethanol (-grade reagent, purity, 99.5%, specific gravity: approx. 0.8) was dropped was placed on the left end of the tray, and the alcohol absorbent prepared above was placed. It was fixed to the right end of the tray with double-sided tape, and the opening of the plastic film bag was sealed by heat sealing. Two specimens of each of these specimens were prepared, and the change in weight increase over time at room temperature (13° C. to 17° C.) was measured, and an experiment was conducted to compare the amount of ethanol absorbed. The results are shown in Table 1 in the attached sheet.

この実験結果より明らかなように、上記6種類のアルコ
ール吸収剤としてのエタノール吸着能力は、粒状焼成ゼ
オライト〉砂状ヤシガラ活性炭〉粒状セピオライト〉粉
状セピオライト〉亜硫酸カルシウム〉焼石膏の順であっ
た。しかも、いづれも初めの10日間迄の方が、次の1
3日間よりはるかに吸着能力が低下しており、速効性を
示している。
As is clear from the results of this experiment, the ethanol adsorption capacity of the six types of alcohol absorbents listed above was in the following order: granular calcined zeolite, sandy coconut shell activated carbon, granular sepiolite, powdered sepiolite, calcium sulfite, and calcined gypsum. Moreover, in each case, the first 10 days are better than the next 1.
The adsorption capacity was much lower than that for 3 days, indicating fast-acting properties.

実施例2゜ アルコール吸収剤における物理吸着反応剤として焼成ゼ
オライト及び砂状ヤシガラ活性炭を使用し、化学吸収反
応剤すなわち潮解性無機塩類のアルコール付加物生成反
応剤として塩化カルシウム2水塩を使用し、その化学吸
収反応剤がアルコール吸収剤全量の10%、20%、3
3%重量部となるように調整すると共に、各成分を下記
表に示す通りに配合して良く混合せしめ、以下実施例1
と同様にして常温(13℃〜17℃位)での重量増加の
経日変化によるエタノール吸収量の比較実験をした。
Example 2 Calcined zeolite and sandy coconut shell activated carbon are used as physical adsorption reactants in an alcohol absorbent, calcium chloride dihydrate is used as a chemical absorption reactant, that is, an alcohol adduct-forming reactant of deliquescent inorganic salts, The chemical absorption reactant is 10%, 20%, 3% of the total amount of alcohol absorbent.
The content was adjusted to 3% by weight, and each component was blended as shown in the table below and mixed well.
In the same manner as above, an experiment was conducted to compare the amount of ethanol absorbed by the change in weight increase over time at room temperature (approximately 13°C to 17°C).

その結果を次の表2に示す。The results are shown in Table 2 below.

表2 以上の実験結果より、試験体Aの重量増加率は、10日
間で38.98%増、23日間で5339%増、試験体
Bの重量増加率は、10日間で69.09%増、23日
間で87.27%増、試験体Cの重量増加率は、10日
間で94.83%増、23日間で112.07%増(い
ずれも2検体平均)となっているが、実際には3ccの
エタノールを重量換算すると2.4g(比重:0.8の
ため)位であり、重量増加率の最大値は夫々試験体A:
47.06%、B:43.64%、C:41J8%、に
留まるべき数値なのに、化学吸収反応剤(塩化カルシウ
ム2水塩)による潮解性のため吸水現象、即ち、“潮解
液だれ”現象により、重量増加過多の数値が得られてい
る。
Table 2 From the above experimental results, the weight increase rate of test body A was 38.98% increase in 10 days, 5339% increase in 23 days, and the weight increase rate of test body B was 69.09% increase in 10 days. , an increase of 87.27% in 23 days, and the weight increase rate of test specimen C is 94.83% increase in 10 days and 112.07% increase in 23 days (both are averages of 2 samples), but in reality The weight of 3 cc of ethanol is about 2.4 g (because specific gravity: 0.8), and the maximum weight increase rate was for test specimen A:
Although the values should remain at 47.06%, B: 43.64%, and C: 41J8%, water absorption occurs due to the deliquescent property of the chemical absorption reactant (calcium chloride dihydrate), that is, the "deliquescent liquid dripping" phenomenon. Therefore, the numerical value of excessive weight increase was obtained.

また、上記表2中の袋体及び袋体内の状況の項目で明ら
かなように、化学吸収反応剤(塩化カルシウム2水塩)
の使用量に比例して、“潮解液だれ”現象が増加し、ア
ルコール吸収剤としては使用不能であることが判明した
In addition, as is clear from the items of the bag and the situation inside the bag in Table 2 above, the chemical absorption reactant (calcium chloride dihydrate)
It was found that the "deliquescence dripping" phenomenon increased in proportion to the amount of alcohol used, making it unusable as an alcohol absorbent.

実施例3゜ 化学吸収反応剤として粉末塩化カルシウム2水塩の配合
率を5%(重量部)に設定し、物理吸着反応剤として粒
状焼成ゼオライト及び砂状活性炭を併用し、各成分を下
記表に示す通りに配合してアルコール吸収剤を作成し、
実施例1と同様のプラスチックフィルム内に入れたトレ
ーの底部に、上記アルコール吸収剤を敷き、トレーの中
心部に3ccのエタノールを滴下したカット綿を載せ、
実施例2と同様にして常温(16℃〜23℃位)での重
量増加の経口変化による、アルコールの吸収量測定と“
潮解液だれ”現象観察を観察した。
Example 3 The blending ratio of powdered calcium chloride dihydrate as a chemical absorption reaction agent was set to 5% (parts by weight), and granular calcined zeolite and sandy activated carbon were used together as a physical absorption reaction agent, and each component was as shown in the table below. Create an alcohol absorbent by mixing as shown in
The alcohol absorbent was placed on the bottom of a tray placed in the same plastic film as in Example 1, and cut cotton on which 3 cc of ethanol had been dropped was placed in the center of the tray.
In the same manner as in Example 2, the amount of alcohol absorbed was measured by oral change in weight increase at room temperature (approximately 16°C to 23°C).
The deliquescent liquid dripping phenomenon was observed.

その結果を次の表3に示す。The results are shown in Table 3 below.

表3 この実験結果より明らかなように、試験体Bの方が試験
体Aよりアルコールの吸収量は多く、又“潮解液だれ”
現象もなく良好な結果が得られた。
Table 3 As is clear from the results of this experiment, test specimen B absorbed more alcohol than test specimen A, and “deliquescence dripped”.
Good results were obtained without any phenomena.

因みに、アルコールの吸収量は、試験体Aの重量増加率
(2検体平均)は、2日間で13.08%増、7日間で
は、1636%増、試験体Bの重量増加率(2検体平均
)は、2日間では、1682%増、7日間では、20.
09%増、の結果を得た。
Incidentally, regarding the amount of alcohol absorbed, the weight increase rate of test specimen A (average of 2 specimens) increased by 13.08% in 2 days, 1636% increase in 7 days, and the weight increase rate of specimen B (average of 2 specimens). ) increased by 1682% in 2 days and by 20% in 7 days.
The result was an increase of 0.09%.

エタノールの添加量が、実施例2と同様に3ccである
ので、重量換算で2.4g位となり、試験体A、  B
共に、重量増加率の最大値は、22.43%に留まる。
Since the amount of ethanol added was 3 cc as in Example 2, the weight was approximately 2.4 g, and the test specimens A and B
In both cases, the maximum weight increase rate remains at 22.43%.

従って、試験体A、Bの7日間後のエタノール吸収率は
、試験体Aの場合72.94%、試験体Bの場合89.
57%となり、試験体Bは試験体Aよりも高いアルコー
ル吸収率が得られると同時に、“潮解液だれ”現象もな
い極めて優れたアルコール吸収剤であることが理解され
る。
Therefore, the ethanol absorption rates of specimens A and B after 7 days were 72.94% for specimen A and 89.9% for specimen B.
57%, and it is understood that test specimen B has a higher alcohol absorption rate than test specimen A, and at the same time is an extremely excellent alcohol absorbent without the "deliquescent liquid dripping" phenomenon.

実施例4゜ 化学吸収反応剤として、塩化カルシウム2水塩。Example 4゜ Calcium chloride dihydrate as a chemical absorption reactant.

塩化鉄水和物、亜塩素酸ナトリウム+過炭酸ナトリウム
3水塩、を使用し、物理吸着反応剤として粒状ゼオライ
ト及び砂状活性炭を併用し、塩化カルシウム2水塩を5
重量%と10重量%に設定する   ゛と共に、塩化鉄
水和物を5重量%に、亜塩素酸ナトリウム9重量%十過
炭酸ナトリウム1重量%の配合率に設定し、下記の表に
示す通りに配合し、実施例3と同様にして常温(21℃
〜25℃位)での重量増加の経口変化による、アルコー
ルの吸収量測定と“潮解液だれ”現象観察を観察した。
Using iron chloride hydrate, sodium chlorite + sodium percarbonate trihydrate, and using granular zeolite and sandy activated carbon as physical adsorption reagents, calcium chloride dihydrate was added to
% by weight and 10% by weight, iron chloride hydrate was set to 5% by weight, sodium chlorite was set to 9% by weight, and sodium percarbonate was 1% by weight, as shown in the table below. in the same manner as in Example 3 at room temperature (21°C).
The amount of alcohol absorbed was measured and the "deliquescence dripping" phenomenon was observed based on the oral change in weight increase at a temperature of ~25°C.

その結果を次の表4に示す。The results are shown in Table 4 below.

表4 この実験結果より明らかなように、試験体C9D、  
Eは試験体A、  Bと比較して、“潮解液だれ”現象
やアルコール吸収率では大きな差異はなかったが、アル
コール吸収剤の包装袋に異変を生じたり、塩素臭を発生
したため、実質上の使用は不能であると言える。
Table 4 As is clear from the results of this experiment, test specimen C9D,
Compared with test samples A and B, there was no major difference in the "deliquescent liquid dripping" phenomenon or alcohol absorption rate, but the packaging bag of the alcohol absorbent changed and a chlorine odor was generated, so it was practically It can be said that the use of is impossible.

やはり、潮解性物質としては塩化カルシウム2水塩が、
現在までの実験結果より最も有効であると推察出来る。
As expected, calcium chloride dihydrate is the deliquescent substance.
It can be inferred that this is the most effective method based on the experimental results to date.

実施例5゜ アルコール吸収剤として、袋体内のアルコール吸収剤約
Logに対して塩化カルシウム2水塩の粉末状を5%(
重量%)、粒状を20%(重量%)に調整作成し、別紙
の表5に示す通りに配合し、実施例4と全く同一の方法
でA−Cの試験体を各2検体づつ作成し、常温(21℃
〜25℃位)での重量増加の経日変化による、アルコー
ルの吸収量測定と“潮解液だれ”現象観察を観察した。
Example 5 As an alcohol absorbent, powdered calcium chloride dihydrate was added in an amount of 5% (about Log of the alcohol absorbent in the bag).
(wt%), the granules were adjusted to 20% (wt%), mixed as shown in Table 5 in the attached sheet, and two specimens of each of A to C were created in exactly the same manner as in Example 4. , normal temperature (21℃
The amount of alcohol absorbed was measured and the "deliquescence dripping" phenomenon was observed based on the change in weight increase over time at a temperature of ~25°C.

その結果を次の表6に示す。The results are shown in Table 6 below.

表6 実験開始後、3日目でパック内のトレー上にアルコール
液が残留していた試験体は、試験体Aだけであった。7
日目に重量測定後、“潮解液だれ”現象による袋濡れが
全く確認出来なかったので、更に2ccのエタノールを
添加した。実験の結果より明らかなように、13日間後
に試験体BとCには袋濡れ現象が観察され、試験体Aは
僅かであった。
Table 6 Test specimen A was the only specimen in which alcohol solution remained on the tray in the pack on the third day after the start of the experiment. 7
After measuring the weight on the second day, no bag wetting due to the "deliquescence dripping" phenomenon could be confirmed, so 2 cc of ethanol was added. As is clear from the results of the experiment, after 13 days, the bag wetting phenomenon was observed in specimens B and C, and was slight in specimen A.

因みに、7日間後のアルコール吸収率の2検体平均は、
夫々試験体A70.83%、試験体B77.08%、試
験体C75,00%、であった。
Incidentally, the average of the two samples of alcohol absorption rate after 7 days is
They were 70.83% for test piece A, 77.08% for test piece B, and 75.00% for test piece C, respectively.

実施例6゜ アルコール吸収剤として塩化カルシウム2水塩。Example 6゜ Calcium chloride dihydrate as an alcohol absorbent.

軽焼マグネシア、無水硫酸マグネシウム、合成けい酸ア
ルミニウムを使用し、別紙表7のような配合率(重量%
)に調整し、実施例4と同様な方法で作成した試験体A
−Hの試験体をトレーの下に敷き、トレー上に直接3c
cのエタノールをピペットにて滴下した。これらの試験
体を各2検体づつ作成し、常温(22℃〜26℃位)で
、2日間は残留アルコール液の有無を、4日間、11日
間では、試験体の重量増加の経日変化の測定と、11日
間後の“潮解液だれ”現象を観察した。
Lightly calcined magnesia, anhydrous magnesium sulfate, and synthetic aluminum silicate are used, and the compounding ratio (wt%) as shown in Appendix Table 7 is used.
) and prepared in the same manner as in Example 4.
- Place the test specimen of H under the tray, and place 3c directly on the tray.
Ethanol (c) was added dropwise using a pipette. Two specimens of each of these specimens were prepared and kept at room temperature (about 22°C to 26°C) for 2 days to check for the presence or absence of residual alcohol solution, and for 4 and 11 days to check for changes in the weight increase of the specimens over time. The measurement and the "deliquescence dripping" phenomenon after 11 days were observed.

その結果を別紙の表8に示す。The results are shown in Table 8 in the attached sheet.

この実験結果より、実験開始2日後において、試験体A
、  B、  C,D、 Hには残留エタノール液がな
く、試験体E、  F、 Gには残留エタノール液かあ
り、試験体A、  B、  C,D、  Hのアルコー
ル吸収力が良いことが判明した。また、この観察結果よ
り、“潮解液だれ”現象は、試験体Aだけに現れた。
From this experimental result, two days after the start of the experiment, test specimen A
, B, C, D, and H had no residual ethanol liquid, and test specimens E, F, and G had residual ethanol liquid, indicating that test specimens A, B, C, D, and H had good alcohol absorption ability. found. Moreover, from this observation result, the "deliquescent liquid dripping" phenomenon appeared only in test specimen A.

実施例7゜ 従来より、包装食品の鮮度保持のため広範囲に使用され
ている、高純度のエタノール液に鮮度保持液を混和せし
めた、鮮度保持用エタノール水液を使用し、実施例6と
同様な実験を行なった。
Example 7 Same as Example 6, using an aqueous freshness-preserving ethanol solution made by mixing a freshness-preserving liquid with a high-purity ethanol solution, which has been widely used for preserving the freshness of packaged foods. We conducted an experiment.

鮮度保持用エタノール水液の調整 純度99.5%のエタノール液70ccに、水道水25
ccを加え、鮮度保持剤としてL−アスコルビン酸を3
.0g、dl−りんご酸を1.0g、ソルビン酸を1.
0g、夫々溶かして、鮮度保持用エタノール水液とする
Adjustment of ethanol aqueous solution for freshness preservation Add 25 ml of tap water to 70 cc of ethanol solution with a purity of 99.5%.
cc and L-ascorbic acid as a freshness preserving agent.
.. 0g, dl-malic acid 1.0g, sorbic acid 1.0g.
0 g, respectively, to make an ethanol aqueous solution for keeping freshness.

次に、実施例6において優れていた試験体B。Next, test specimen B was excellent in Example 6.

C,Dと同様なアルコール吸収剤を下記表の通りに作成
し、上記作成した鮮度保持用エタノール水液4ccをプ
ラスチックトレー上に直接滴下した以外は前記実施例6
と同様にした。
Example 6 except that alcohol absorbents similar to those in C and D were prepared according to the table below, and 4 cc of the freshness-preserving ethanol aqueous solution prepared above was dropped directly onto the plastic tray.
I did the same thing.

この試験体を各2検体づつ作成し、常温(22〜26℃
位)放置で、4日間後の残留アルコール水液の有無、及
び4日間、11日間後の試験体の重量増加の経口変化の
測定と、11日間後の“潮解液だれ”現象並びに、袋及
び袋内の状況を観察した。
Prepare two specimens of each of these specimens and store them at room temperature (22-26°C
1) After 4 days of standing, the presence or absence of a residual alcohol solution, the oral change in weight increase of the test specimen after 4 days and 11 days, the "deliquescence dripping" phenomenon after 11 days, and the bag and I observed the situation inside the bag.

その結果を次の表9に示す。The results are shown in Table 9 below.

表9 エタノール水液吸収剤の重量増加の経日変化この実験結
果より、残留エタノール水液が観察されなかったのは、
実験開始後48目の試験体B゛だけてあった。以上の結
果、試験体B′の配合組成物が最適であるように推察さ
れる。
Table 9 Change in the weight increase of the ethanol aqueous absorbent over time From the results of this experiment, the reason why no residual ethanol aqueous solution was observed is that
There was only the 48th test specimen B after the start of the experiment. From the above results, it is inferred that the blended composition of test specimen B' is optimal.

実施例8゜ 袋内に残留するエタノール水液の除去及び鮮度保持用有
機酸臭の除去の問題点を解消するために、乾燥粉末消石
灰を混和せしめ、塩化カルシウム2水塩と合成けい酸ア
ルミニウムを下記の表の通りに配合せしめ、実施例7と
同様な実験を行なう。
Example 8 In order to solve the problem of removing the ethanol aqueous solution remaining in the bag and the organic acid odor for preserving freshness, dry powdered slaked lime was mixed with calcium chloride dihydrate and synthetic aluminum silicate. The ingredients were mixed according to the table below, and an experiment similar to Example 7 was conducted.

この試験体を各3検体づつ作成し、実施例7で作成した
鮮度保持用エタノール水液3ccをプラスチックトレー
上に直接滴下して、常温(22〜26℃位)放置で、各
々3日、7日、14日、後の重量測定と残留液の有無、
アルコール臭、酸臭の除去。
Three samples of each of these test specimens were prepared, and 3 cc of the freshness-preserving ethanol aqueous solution prepared in Example 7 was dropped directly onto a plastic tray, and left at room temperature (approximately 22 to 26 degrees Celsius) for 3 days and 7 days, respectively. 14 days later, weight measurement and presence or absence of residual liquid,
Removes alcohol and acid odors.

“潮解液だれ”現象9袋及び袋内の状況について観察し
た。
The nine bags and the conditions inside the bags were observed for the "deliquescence dripping" phenomenon.

その結果を次の表10に示す。The results are shown in Table 10 below.

表10 エタノール水液吸収剤の重量増加の径日変化尚、実験開
始後、3日間の観察状況は、試験体Aの場合、残留液多
く、アルコール臭、酸臭あり。
Table 10: Daily change in weight increase of ethanol aqueous absorbent Note that the observation status for 3 days after the start of the experiment was that in the case of test specimen A, there was a lot of residual liquid, and there was an alcohol odor and an acid odor.

袋溝れなしく△)。試験体Bの場合、残留液僅か。△) In the case of test specimen B, there was only a small amount of residual liquid.

アルコール臭、酸臭残り1袋溝れなしく◎)。試験体C
の場合、残留液少し、アルコール臭、酸臭あり1袋溝れ
あり(○)であった。又、14日間後の観察結果も、試
験体B>C>A、となっており、経日変化の状況に変化
は観られなかった。
Alcohol smell, sour smell left in 1 bag without leaving any residue ◎). Test specimen C
In the case of , there was a little residual liquid, alcohol odor, acid odor, and one bag had grooves (○). Furthermore, the observation results after 14 days also showed that test specimen B>C>A, and no change was observed in the condition of deterioration over time.

尚、各成分の配合割合について述べれば、基盤となる物
理吸着反応剤としての多孔質性物質については全成分の
95重量%位まで使用可能であり、アルコール付加物生
成可能な化学吸収反応剤については全成分の約15重量
%位まで使用可能であが、対象包装食品や使用原料によ
って、その配合割合を変える必要がある。即ち、含水量
の多い包装食品の場合には、食品の水分によるアルコー
ル吸収剤の水濡れを防止するために、例えば粉状焼成ゼ
オライ50重量%に砂状活性炭35重量%を加え、塩化
カルシウム2水塩5重量%を混和させ、更にこの混和物
に焼成マグネシア10重量%を加えてアルコール吸収剤
を調整すれば良い。又、保香性を重視する包装食品の場
合には、取香性を有する活性炭のような多孔質性吸着物
質をさけ、例えば粒状乾燥ゼオライト80重量%に塩化
カルシウム2水塩10重量%を混和させ、粉末消石灰1
0重量%を加えてアルコール吸収剤を調整すれば良い。
Regarding the blending ratio of each component, it is possible to use up to 95% by weight of the porous material as the base physical adsorption reactant, and the chemical absorption reactant capable of producing alcohol adducts. Although it is possible to use up to about 15% by weight of the total ingredients, it is necessary to change the blending ratio depending on the target packaged food and the raw materials used. That is, in the case of packaged foods with a high water content, in order to prevent the alcohol absorbent from getting wet due to the water content of the food, for example, 35% by weight of sandy activated carbon is added to 50% by weight of powdered calcined zeolite, and 2% calcium chloride is added. An alcohol absorbent may be prepared by mixing 5% by weight of aqueous salt and further adding 10% by weight of calcined magnesia to this mixture. In addition, in the case of packaged foods where aroma retention is important, porous adsorbents such as activated carbon that have aroma absorption properties should be avoided, and for example, 80% by weight of granular dry zeolite should be mixed with 10% by weight of calcium chloride dihydrate. Powdered slaked lime 1
The alcohol absorbent may be adjusted by adding 0% by weight.

一般に含水量の少なめな包装食品の場合、粒状乾燥ゼオ
ライトや砂状活性炭2粒状セピオライト等の多孔質性物
質の単体又は2種類以上を混和したものを95重量%に
塩化カルシウム・2水塩5重量%を加えてアルコール吸
収剤を調整すれば良い。
In general, in the case of packaged foods with a low water content, 95% by weight of porous substances such as granular dry zeolite, sandy activated carbon, 2 granular sepiolite, etc. or a mixture of two or more types of porous substances are added to 5% by weight of calcium chloride dihydrate. You can adjust the alcohol absorbent by adding %.

〈発明の効果〉 本発明に係るアルコール吸収剤は、有機酸を使用した鮮
度保持液との併用においても、酸臭除去効果、余剰水分
除去効果、及び“潮解液だれ”現象の防止効果、にまで
至る全ての併発障害をも除去出来、極めて優れたアルコ
ール吸収剤と言える。
<Effects of the Invention> The alcohol absorbent according to the present invention has the effect of removing acid odor, the effect of removing excess water, and the effect of preventing the "deliquescence dripping" phenomenon, even when used in combination with a freshness-preserving liquid using an organic acid. It can be said to be an extremely excellent alcohol absorbent, as it can eliminate all the accompanying disorders.

Claims (1)

【特許請求の範囲】[Claims] 多孔質性物質からなる物理吸着反応剤と、化学吸収反応
剤としてのアルコール付加物生成可能な潮解性無機塩、
有機酸、有機酸塩から選ばれた1種もしくは2種以上の
成分とから成ることを特徴とする包装食品のアルコール
吸収剤。
A physical adsorption reactant made of a porous material, a deliquescent inorganic salt capable of producing alcohol adducts as a chemical absorption reactant,
An alcohol absorbent for packaged foods characterized by comprising one or more components selected from organic acids and organic acid salts.
JP2326519A 1990-11-27 1990-11-27 Alcohol absorbent for packaged food Pending JPH04190772A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2326519A JPH04190772A (en) 1990-11-27 1990-11-27 Alcohol absorbent for packaged food

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2326519A JPH04190772A (en) 1990-11-27 1990-11-27 Alcohol absorbent for packaged food

Publications (1)

Publication Number Publication Date
JPH04190772A true JPH04190772A (en) 1992-07-09

Family

ID=18188740

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2326519A Pending JPH04190772A (en) 1990-11-27 1990-11-27 Alcohol absorbent for packaged food

Country Status (1)

Country Link
JP (1) JPH04190772A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007236245A (en) * 2006-03-07 2007-09-20 Ueno Fine Chem Ind Ltd Alcohol volatile agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007236245A (en) * 2006-03-07 2007-09-20 Ueno Fine Chem Ind Ltd Alcohol volatile agent

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