JPH03200546A - Package of oxygen absorbent - Google Patents
Package of oxygen absorbentInfo
- Publication number
- JPH03200546A JPH03200546A JP34118789A JP34118789A JPH03200546A JP H03200546 A JPH03200546 A JP H03200546A JP 34118789 A JP34118789 A JP 34118789A JP 34118789 A JP34118789 A JP 34118789A JP H03200546 A JPH03200546 A JP H03200546A
- Authority
- JP
- Japan
- Prior art keywords
- film
- paper
- packaging material
- air permeability
- water
- 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
Links
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title claims abstract description 49
- 239000001301 oxygen Substances 0.000 title claims abstract description 49
- 229910052760 oxygen Inorganic materials 0.000 title claims abstract description 49
- 230000002745 absorbent Effects 0.000 title 1
- 239000002250 absorbent Substances 0.000 title 1
- 230000035699 permeability Effects 0.000 claims abstract description 37
- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000002985 plastic film Substances 0.000 claims abstract description 9
- 229920006255 plastic film Polymers 0.000 claims abstract description 9
- 229920005989 resin Polymers 0.000 claims abstract description 9
- 239000011347 resin Substances 0.000 claims abstract description 9
- 239000005022 packaging material Substances 0.000 claims description 45
- 239000006096 absorbing agent Substances 0.000 claims description 36
- 239000012982 microporous membrane Substances 0.000 claims description 14
- 229920003023 plastic Polymers 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 abstract description 9
- 230000001070 adhesive effect Effects 0.000 abstract description 9
- 238000010521 absorption reaction Methods 0.000 abstract description 3
- 239000002650 laminated plastic Substances 0.000 abstract 2
- 239000000123 paper Substances 0.000 description 54
- 239000003921 oil Substances 0.000 description 13
- 235000013305 food Nutrition 0.000 description 12
- 238000007789 sealing Methods 0.000 description 12
- 239000004698 Polyethylene Substances 0.000 description 10
- 238000003475 lamination Methods 0.000 description 10
- 229940123973 Oxygen scavenger Drugs 0.000 description 9
- 239000012528 membrane Substances 0.000 description 9
- -1 polyethylene Polymers 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- 239000000565 sealant Substances 0.000 description 7
- 238000002844 melting Methods 0.000 description 6
- 230000002000 scavenging effect Effects 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 229920000690 Tyvek Polymers 0.000 description 5
- 239000004775 Tyvek Substances 0.000 description 5
- 239000012790 adhesive layer Substances 0.000 description 5
- 238000010030 laminating Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 229920001684 low density polyethylene Polymers 0.000 description 3
- 239000004702 low-density polyethylene Substances 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 239000005001 laminate film Substances 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000009920 food preservation Methods 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 229940079826 hydrogen sulfite Drugs 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000002651 laminated plastic film Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 239000011088 parchment paper Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 235000021067 refined food Nutrition 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000009823 thermal lamination Methods 0.000 description 1
Landscapes
- Bag Frames (AREA)
- Packages (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、脱酸素剤包装体に係り、さらに詳しくは、脱
酸素剤を特定のラミネート構成からなる特定の透気度を
有する包装材料で包装した脱酸素剤包装体に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to an oxygen absorber package, and more particularly, the present invention relates to an oxygen absorber package, and more specifically, the present invention relates to an oxygen absorber package, and more specifically, an oxygen absorber packaged in a packaging material having a specific laminate structure and a specific air permeability. This invention relates to a packaged oxygen absorber package.
本発明は、それを構成する脱酸素剤用包装材料の製造及
び製袋が容易であるばかりでなく、脱酸素剤用包装材料
が安定した透気性、ラミネート強度、シール強度を有し
、耐水性、耐酸性、耐アルコール性などの耐久性に優れ
るため安定した脱酸素性能を発揮し、多くの加工食品等
の保存剤として好適に使用される。The present invention not only facilitates the production and bag making of the oxygen absorber packaging material that constitutes the oxygen absorber packaging material, but also enables the oxygen absorber packaging material to have stable air permeability, lamination strength, seal strength, and water resistance. It exhibits stable oxygen scavenging performance due to its excellent durability such as acid resistance and alcohol resistance, and is suitably used as a preservative for many processed foods.
脱酸素剤は、酸素を吸収する性質を有する組成物からな
り、通常、通気性の小袋に封入して用いられる。Oxygen scavengers are made of a composition that has the property of absorbing oxygen, and are usually used by being enclosed in a breathable pouch.
一般に、通気性小袋を構成する包装材料には、例えば、
紙と有孔ポリエチレンフィルムをラミネ−トシた包装材
料、穿孔プラスチックフィルムと紙と有孔ポリエチレン
フィルムを積層接着した包装材料、不織布や微多孔膜な
どを使用した包装材料等が用いられている。In general, the packaging materials that make up breathable sachets include, for example:
Packaging materials in which paper and perforated polyethylene film are laminated, packaging materials in which perforated plastic film, paper, and perforated polyethylene film are laminated and bonded together, and packaging materials using nonwoven fabrics, microporous membranes, and the like are used.
脱酸素剤包装材料の脱酸素剤保存技術上の問題点として
、脱酸素剤は、乾燥食品、高水分食品、酸性食品、油加
工食品、アルコール含有食品等の種々の食品に使用する
ため、脱酸素剤組成物中に含まれる水分が乾燥食品に移
行し脱酸素性能が損われたり、高水分食品の水分が、脱
酸素剤組成物に移行するため、包材の表面に染みが発生
し外観を損なったり、食品の油が包材にしみ込み、包材
の透気性が損なわれて、脱酸素性能が損われるなどがあ
げられる。かかる欠点のために、脱酸素剤を使用する状
況に応じて、包材の材質構成をかえて対応しているが、
完全な脱酸素剤用包装材料とはなっていない。Oxygen absorber Packaging materials have a technical problem in preserving oxygen absorbers. Oxygen absorbers are used in various foods such as dry foods, high-moisture foods, acidic foods, oil-processed foods, and alcohol-containing foods. Moisture contained in the oxygen absorber composition transfers to dry foods, impairing oxygen scavenging performance, and moisture from high-moisture foods transfers to the oxygen scavenger composition, causing stains on the surface of the packaging material and impairing its appearance. Food oils may seep into the packaging material, impairing its air permeability and deoxidizing performance. Due to these drawbacks, the material composition of the packaging material is changed depending on the situation in which the oxygen absorber is used.
It is not a perfect packaging material for oxygen absorbers.
近年は、脱酸素剤の適用分野が多岐にわたり、使用条件
が過、酷となる傾向にあるため、微多孔膜などを用いた
耐久性の優れた包装材料が多用されている。In recent years, oxygen scavengers have been applied to a wide range of fields and the conditions of use have become harsher and harsher, so highly durable packaging materials using microporous membranes and the like have come into widespread use.
また、フィルムラミネートには、ポリエチレン、ポリエ
チレン酢ビ共重合体、アイオノマー樹脂等からなる低融
点のシーラントフィルムを接着層として熱ラミネートす
るのが一般的であるが、この方法においては、熱ラミネ
ート加工の際に低融点フィルムが熔融し、シーラントフ
ィルムに開孔された孔がふさがり透気性が低下すること
などから、安定した透気度を付与する事が困難である。In addition, it is common for film lamination to be thermally laminated using a low melting point sealant film made of polyethylene, polyethylene vinyl acetate copolymer, ionomer resin, etc. as an adhesive layer; It is difficult to provide stable air permeability because the low melting point film melts and the pores in the sealant film become clogged, reducing air permeability.
又、透気度を確保するために、低温のラミネート条件を
採用すると十分なラミネート強度を得る事ができない。Furthermore, if low temperature lamination conditions are used to ensure air permeability, sufficient lamination strength cannot be obtained.
つまり従来の熱ラミネート加工法では、包装材料の製造
及び製袋が容易で、かつ、安定した透気性、ラミネート
強度、シール強度を有し、更に耐水性、耐酸性、耐アル
コール性などの耐久性に優れ、安定した脱酸素性能を発
揮する脱酸素剤用の包装材料を加工する事は困難である
。In other words, with conventional thermal lamination processing methods, it is easy to manufacture packaging materials and form bags, and it has stable air permeability, lamination strength, and sealing strength, as well as durability such as water resistance, acid resistance, and alcohol resistance. It is difficult to process packaging materials for oxygen scavengers that exhibit excellent and stable oxygen scavenging performance.
一方不織布、微多孔膜、耐水耐油性加工紙等の微多孔フ
ィルムを用いた包装材料として、これらの微多孔フィル
ムにポリエチレン、ポリエチレン酢ビ共重合体、アイオ
ノマー樹脂等からなる低融点のシーラントフィルムを熱
ラミネートとたものが多く使用されているが、熱ラミネ
ート加工の際に低融点フィルムが熔融し、シーラントフ
ィルムに開孔された孔がふさがり、透気性が低下し安定
した透気度を確保する事は困難であること、また透気度
を確保するために、低温のラミネート条件を採用すると
十分なラミネート強度を得る事ができないなど、脱酸素
剤用包装材料として、不満足であった。On the other hand, as packaging materials using microporous films such as nonwoven fabrics, microporous membranes, and water- and oil-resistant treated papers, low-melting point sealant films made of polyethylene, polyethylene vinyl acetate copolymers, ionomer resins, etc. are applied to these microporous films. Heat lamination is often used, but during heat lamination, the low melting point film melts and the holes made in the sealant film are closed, reducing air permeability and ensuring stable air permeability. However, it was unsatisfactory as a packaging material for oxygen absorbers because it was difficult to obtain sufficient lamination strength when low-temperature lamination conditions were used to ensure air permeability.
本発明は、製造及び製袋が容易で、かつ、安定した透気
性、シール強度、ラミネート強度を有し、更に耐水性、
耐酸性、耐アルコール性などの耐久性に優れ、安定した
脱酸素性能を発揮する脱酸素剤用包装材料で脱酸素剤を
包装した脱酸素剤包装体を提供することを目的とする。The present invention is easy to manufacture and form bags, has stable air permeability, sealing strength, and lamination strength, and has water resistance and
An object of the present invention is to provide an oxygen absorber package in which an oxygen absorber is packaged using a packaging material for an oxygen absorber that has excellent durability such as acid resistance and alcohol resistance, and exhibits stable oxygen scavenging performance.
本発明者等は、前記目的を遠戚すべく鋭意研究した結果
、不織布、微多孔膜、耐水耐油性加工紙等の微多孔フィ
ルムに、これらよりも低融点のシーラントフィルム以外
の樹脂フィルムをラミネートすることにより、透気性に
優れた積層フィルムが得られることを見出し、本発明を
完成した。As a result of intensive research aimed at distantly related to the above-mentioned object, the inventors of the present invention have found that microporous films such as nonwoven fabrics, microporous membranes, and water- and oil-resistant treated paper are laminated with resin films other than sealant films having a lower melting point than these films. It was discovered that a laminated film with excellent air permeability could be obtained by doing so, and the present invention was completed.
本発明は、常圧で水を通さない不織布、微多孔膜である
プラスチックフィルムおよび耐水耐油性加工紙よりなる
群から選ばれた1種の微細孔を有するフィルム(A)と
、(A)と同等以下の軟化点を有する樹脂からなるガー
レー式透気度が0,1〜1.000秒/100−の微多
孔膜(B)とを貼り合わせてなるガーレー式透気度が1
〜10,000秒/100−であるプラスチック積層フ
ィルム(C)からなる包装材料を、脱酸素剤の包装材料
の全部もしくは一部として用い該包装材料の(A)を外
側にして脱酸素剤を包装しシールしたことを特徴とする
脱酸素剤用包装体である。(第3図参照)本発明におい
て、微細孔を有するフィルム<A)は、常圧で水を通さ
ない不織布、微多孔膜であるプラスチックフィルムおよ
び耐水耐油性加工紙よりなる群から選ばれる1種である
。The present invention provides a film (A) having one kind of micropores selected from the group consisting of a nonwoven fabric that does not pass water under normal pressure, a microporous plastic film, and a water- and oil-resistant treated paper; A microporous membrane (B) with a Gurley air permeability of 0.1 to 1.000 seconds/100-, which is made of a resin having a softening point equal to or lower than the above, is laminated with a Gurley air permeability of 1.
A packaging material made of a plastic laminated film (C) with a speed of ~10,000 seconds/100- is used as all or part of the packaging material for an oxygen absorber, and the oxygen absorber is placed with (A) of the packaging material on the outside. This is a package for an oxygen absorber characterized by being packaged and sealed. (See Figure 3) In the present invention, the film with micropores <A) is one type selected from the group consisting of nonwoven fabrics that do not allow water to pass through under normal pressure, plastic films that are microporous membranes, and water- and oil-resistant treated paper. It is.
常圧で水を通さない不織布は、ガーレー式透気度が0.
01〜1.000秒/10〇−程度の通気性を有し、か
つ常圧で水を通さないポリオレフィン、ポリエステル等
の不織布であり、例えば、タイベック(デュポン社製)
、ルクサー(旭化戊工業製)などの市販品を挙げること
ができる。Nonwoven fabrics that do not allow water to pass through under normal pressure have a Gurley air permeability of 0.
It is a nonwoven fabric made of polyolefin, polyester, etc., which has an air permeability of about 01 to 1.000 seconds/100- and does not allow water to pass through at normal pressure, such as Tyvek (manufactured by DuPont).
, Luxar (manufactured by Asahi Kabo Kogyo Co., Ltd.) and other commercially available products.
微多孔膜であるプラスチックフィルムは、ポリエチレン
、ポリプロピレンなどの合成樹脂フィルムを延伸して製
造する際、シリカ、タルク、炭酸カルシウム等の微粉末
を添加してフィルムを延伸し、該フィルムから微粉末を
抽出するなどの方法により製造される孔径が0.01〜
50μmの微細孔を有するガーレー式透気度が0.1〜
1.000秒/10〇−程度の常圧で水を通さないプラ
スチックフィルムである。例えば、NFレシート徳山曹
達■製)、ボーラム(徳山曹達■製〉、セルポアー(種
水化学工業■製)、FP−2(旭化或工業■製) 、N
OP (日本石油化学IJ@製)、ニドフロンNTF
(日東電気工業■製)、ポリフロンペーノで−(ダイキ
ン工業■製)、ジュラガード(セラニーズ社製)、コー
アテックス(ボア社製)等の市販品を挙げることができ
る。Plastic films, which are microporous membranes, are produced by stretching a synthetic resin film such as polyethylene or polypropylene, by adding fine powder such as silica, talc, or calcium carbonate, stretching the film, and extracting the fine powder from the film. The pore size produced by a method such as extraction is 0.01~
Gurley type air permeability with 50μm micropores is 0.1~
It is a plastic film that does not allow water to pass through under normal pressure of about 1.000 seconds/100. For example, NF Receipt (manufactured by Tokuyama Soda ■), Bolam (manufactured by Tokuyama Soda ■), Cellpore (manufactured by Tanemizu Chemical Industry ■), FP-2 (manufactured by Asahi Kakogyo ■), N
OP (manufactured by Nippon Petrochemical IJ@), Nidoflon NTF
Commercially available products include (manufactured by Nitto Electric Industries, Ltd.), Polyfuronpeno (manufactured by Daikin Industries, Ltd.), Duraguard (manufactured by Celanese Corporation), and Coatex (manufactured by Boa Corporation).
耐水耐油加工紙は、一般に、耐油紙、耐潤紙、耐湿紙、
耐水撥水紙などといわれているものである。具体的には
、塗工印刷用紙(アート紙、コート紙、グラビア紙など
)、情報記録紙、電気絶縁紙、剥離紙、離型紙、段ボー
ル紙、紙器用板紙、化粧板原紙、食品包装用加工紙、食
品包装用カートン紙等の種々の紙のうち、主として、食
品包装用の加工紙に属するもの、及び、紙とプラスチ・
ツクの混抄紙が適当である。又、加工紙には硫酸紙など
の酸処理をした化学処理紙、WS紙、MC紙、フィルタ
紙、グラシン紙、WO2紙などの抄紙工程で合成樹脂な
どを抄き込んだ紙、及び塗工紙(ワックス紙、フッ素加
工紙、塩化ビニリデン加工紙、pvc加工紙、PE加工
紙、ラッカーコート紙など)、ラミネート紙等の抄紙後
に物理的処理を施して加工した紙などがある。Water and oil resistant treated paper is generally oil resistant paper, moisture resistant paper, moisture resistant paper,
This is called water-resistant and water-repellent paper. Specifically, coated printing paper (art paper, coated paper, gravure paper, etc.), information recording paper, electrical insulation paper, release paper, release paper, corrugated paper, folding carton paperboard, base paper for decorative laminates, processing for food packaging. Among various papers such as paper and carton paper for food packaging, mainly those belonging to processed paper for food packaging, and paper and plastic paper.
Tsuku mixed paper is suitable. In addition, processed paper includes chemically treated paper that has been acid-treated such as parchment paper, WS paper, MC paper, filter paper, glassine paper, WO2 paper that has synthetic resin added during the papermaking process, and coated paper. Papers include paper (wax paper, fluorine-processed paper, vinylidene chloride-processed paper, PVC-processed paper, PE-processed paper, lacquer coated paper, etc.), laminated paper, and other papers that are processed by physical processing after papermaking.
好適な加工紙は、坪量が10 = 100 g/m’。A suitable processed paper has a basis weight of 10 = 100 g/m'.
好ましくは20〜60g/m’の厚紙で先に示した方法
で、耐水耐油加工したものである。坪量が小さすぎると
加工性、耐久性などに欠け、大きすぎると包材のコシが
強く、脱酸素剤充填が困難である。Preferably, the paper is made of cardboard having a weight of 20 to 60 g/m' and has been treated to be water and oil resistant by the method described above. If the basis weight is too small, workability and durability will be lacking, and if it is too large, the packaging material will be stiff and difficult to fill with an oxygen scavenger.
一方前記(A)微細孔を有するフィルムと貼り合わせる
微多孔膜(B)は、(A)で使用するフィルムと同等以
下、好ましくは10℃以下の軟化点を有する前記<A)
で例示した微多孔膜からなるプラスチックフィルムと同
種の樹脂フィルムである。On the other hand, the microporous film (B) to be bonded to the film having micropores (A) has a softening point equal to or lower than that of the film used in (A), preferably 10°C or lower.
This is the same type of resin film as the plastic film made of microporous membrane exemplified in .
プラスチック積層フィルム(C)は、前記(A)と(B
)とを、120〜200℃程度の温度でヒートシールに
て貼り合わせたガーレー式透気度が1〜10,000秒
/100−のラミネートフィルムからなる包装材料であ
る。The plastic laminated film (C) consists of the above (A) and (B).
) are laminated together by heat sealing at a temperature of about 120 to 200°C and have a Gurley air permeability of 1 to 10,000 seconds/100.
(C)において、(B)は接着層として機能するが、ま
た包装材料の補強、透気度の調節と共に、製袋する際の
シール層としても機能する。シール方法としては、ヒー
トシール、接着剤によるシールなどがある。In (C), (B) functions as an adhesive layer, but also functions as a sealing layer during bag making, as well as reinforcing the packaging material and adjusting air permeability. Sealing methods include heat sealing, adhesive sealing, and the like.
前記(C)の包装材料の製袋時の接着強度は、(B)の
樹脂の種類及びフィルムの厚さ、ヒートシール条件など
で変化する。特に、フィルムの厚さが極端に薄い場合は
、接着強度が不足して使用に耐えない。一方、厚すぎた
り、坪量が大きすぎる場合には、ヒートシール時に接着
層で熱間剥離が生じたり、透気度が不安定となり、透気
度を確保する事は困難であり、包装材料のコシが強くな
りフレキシビリティに欠けて使いにくい。The adhesive strength of the packaging material (C) during bag making varies depending on the type of resin (B), the thickness of the film, heat sealing conditions, etc. In particular, if the film is extremely thin, the adhesive strength will be insufficient and it will not be usable. On the other hand, if it is too thick or the basis weight is too large, hot peeling may occur in the adhesive layer during heat sealing, and the air permeability will become unstable, making it difficult to ensure air permeability. It becomes stiff and lacks flexibility, making it difficult to use.
また包装材料の透気度は、使用する(Δ)及び(B)の
種類で決まり、包装材料としての接着強度、製袋の容易
さ、脱酸素剤包装材料の使い易さ、包装密封された脱酸
素剤がこぼれないなどの諸因子を考慮して決められる。The air permeability of the packaging material is determined by the types of (Δ) and (B) used, including adhesive strength as a packaging material, ease of bag making, ease of use of the oxygen absorber packaging material, and whether the package is sealed or not. This is determined by considering various factors such as ensuring that the oxygen absorber does not spill.
特に(B)の厚さが10μm以下の場合接着強度が劣り
、一方300μm以上の場合透気度が不安定となるばか
りでなく、包装材料のコシが強くなり、フレキシビリテ
ィに欠けて使い難く、本発明における脱酸素剤用包装材
料としては不適当である。In particular, if the thickness of (B) is less than 10 μm, the adhesive strength will be poor, while if it is more than 300 μm, not only will the air permeability become unstable, but the packaging material will also become stiff, lacking in flexibility and difficult to use. It is unsuitable as a packaging material for an oxygen absorber in the present invention.
本発明の脱酸素剤包装体は、前記(C)の包装材料を全
部または一部に用い、前記(A)を外側にして脱酸素剤
を包装し、シールしたものである。The oxygen absorber package of the present invention uses the above packaging material (C) in whole or in part, and packages and seals the oxygen absorber with the above (A) on the outside.
但し、本発明の範囲は、以下の実施例により何等の制限
を受けるものではない。However, the scope of the present invention is not limited in any way by the following examples.
(1) 積層プラスチックフィルム(C)(a)
試料C−1
微細孔を有するフィルム(A)としてタイベック105
9B(デュポン社製、ポリエチレン不織布)と、微多孔
膜(B)として厚み35μmのボーラム(徳山曹達■製
、PE微多孔膜)とを100〜12D℃の温度でラミネ
ートして、積層フィルム:試料C−1を調製した。(1) Laminated plastic film (C) (a)
Sample C-1 Tyvek 105 as a film with micropores (A)
9B (manufactured by DuPont, polyethylene nonwoven fabric) and Bolam (manufactured by Tokuyama Soda ■, PE microporous membrane) with a thickness of 35 μm as the microporous membrane (B) were laminated at a temperature of 100 to 12D°C to obtain a laminated film: sample. C-1 was prepared.
これらの脱酸素剤として、亜硫酸塩、亜硫酸水素塩、亜
ニチオン酸塩、ヒドロキノン、カテコール、レゾルシン
、ピロガロール、没食子酸、鉄粉等の金属粉、アスコル
ビン酸等を含有するものが使用される。As these oxygen absorbers, those containing sulfite, hydrogen sulfite, dithionite, hydroquinone, catechol, resorcinol, pyrogallol, gallic acid, metal powder such as iron powder, ascorbic acid, etc. are used.
本発明を、実施例及び比較例により、さらに詳細に説明
する。The present invention will be explained in more detail with reference to Examples and Comparative Examples.
(b) 試料C−2
前記試料C−tの調製において、微多孔膜(B)として
使用した厚み35μmのボーラム(前出)を、厚み50
μmのボーラム(徳山曹達■製、PE微多孔膜)に代え
た以外1よ、試料C−1と全く同様の方法でラミネート
し積層フィルム:試料C−2を調製した。(b) Sample C-2 In the preparation of sample C-t, the 35 μm thick borum (described above) used as the microporous membrane (B) was
A laminated film: Sample C-2 was prepared by laminating in exactly the same manner as Sample C-1, except that the film was replaced with .mu.m Boram (manufactured by Tokuyama Soda ■, PE microporous membrane).
(C) 試料C−3〜C−5
前記試料C−1の調製において、微細孔を有するフィル
ム(A)として使用したタイベック1059B(前出)
をルクサーH1040(旭化戊工業■製、ポリエチレン
不織布)、厚み140μmのNFシートS−140(徳
山曹達■製、PP微多孔膜)及びwop紙(40g/m
’)に代えた以外は試IC−1と全く同様の方法でラミ
ネートし積層フィルム;試料C−3〜C−5を調製した
。(C) Samples C-3 to C-5 Tyvek 1059B (described above) used as the film (A) having micropores in the preparation of sample C-1.
Luxar H1040 (manufactured by Asahi Kabo Industries ■, polyethylene nonwoven fabric), 140 μm thick NF sheet S-140 (manufactured by Tokuyama Soda ■, PP microporous membrane), and WOP paper (40 g/m
Laminated films; Samples C-3 to C-5 were prepared by laminating in exactly the same manner as Sample IC-1 except that Sample IC-1 was replaced with Sample IC-1.
(d) 試料C−6
前記試料C−tのall!III!において、微細孔を
有するフィルム(A)として使用したタイベック105
9B(前出〉をルクサー81040 (前出〉に、微多
孔膜(B)として使用した厚み35μmのボーラム(前
出)を厚み120μmのNFシート (前出)にそれぞ
れ代えて使用する以外は試料C−1と全く同様の方法で
ラミネートし積層フィルム:試料C−6を調製した。(d) Sample C-6 All of the sample C-t! III! Tyvek 105 used as the film (A) with micropores in
The samples were the same except that 9B (previously) was replaced with Luxor 81040 (previously) and the 35 μm thick bolam (previously) used as the microporous membrane (B) was replaced with a 120 μm thick NF sheet (previously). A laminated film: Sample C-6 was prepared by laminating in exactly the same manner as C-1.
(e) 比較試料C[ニー 1〜[:C−4WOP紙
(前出)に、有孔低密度ポリエチレン(B穴)を、90
〜100℃で熱ラミネートし比較試料CC−1とした。(e) Comparative sample C [Knee 1 to [: C-4 WOP paper (previously), perforated low density polyethylene (B holes), 90%
It was thermally laminated at ~100°C to obtain a comparative sample CC-1.
また、比較試料CC−1の有孔低密度ポリエチレン(B
穴)を有孔低密度ポリエチレン〈D穴)にに代えて比較
試料CC−2を、WO2紙をタイベック1059B(前
出)及び、NFシートS−140(前出)に代えて、熱
ラミネートし、比較試料CC−3及びCC−4を調製し
た。In addition, the porous low-density polyethylene (B
Comparative sample CC-2 was heat-laminated by replacing the hole) with perforated low-density polyethylene (D hole), and replacing the WO2 paper with Tyvek 1059B (mentioned above) and NF sheet S-140 (mentioned above). , comparative samples CC-3 and CC-4 were prepared.
(2)包装材料試験
前記第(1)項で調製した各試料及び比較試料について
、透気度、接着強度、ヒートシール強度、製袋性、加工
性及び耐久性の測定を行った。(2) Packaging material test The air permeability, adhesive strength, heat seal strength, bag formability, workability, and durability were measured for each sample prepared in the above item (1) and a comparative sample.
測定結果を第1表に示す。The measurement results are shown in Table 1.
(3)脱酸素剤包装体
前記第(1)項で調製した各試料及び比較試料を用い、
微細孔を有するフィルム(A)面を外側にして5QX5
0m−の包材に製袋し、鉄粉を主剤とする酸素吸収能力
が500itgの脱酸素剤組成物を充填し脱酸素剤包装
体とした。(3) Oxygen absorber package using each sample and comparative sample prepared in the above item (1),
Film with micropores (A) side facing outward 5QX5
A bag was made into a 0 m-thick packaging material, and an oxygen absorber composition containing iron powder as a main ingredient and having an oxygen absorption capacity of 500 itg was filled to obtain an oxygen absorber package.
これらの脱酸素剤包装体及び500−の空気を、酸素バ
リヤー性包材(KON/PE)の袋に入れて密封し、2
5℃に放置した酸素濃度が零になる時間を測定した。These oxygen scavenger packages and 500 ml of air were placed in a bag made of oxygen barrier packaging material (KON/PE) and sealed.
The time for the oxygen concentration to reach zero after being left at 5°C was measured.
サンプル数は各側ともIO点で行った。The number of samples was determined at the IO point on each side.
測定結果を第1表に示す。The measurement results are shown in Table 1.
微多孔膜又は、不織布を用いた従来の脱酸素剤包装体は
、微多孔膜又は、不織布に有孔の低融点のシーラントフ
ィルムをラミネート加工した包装材料を使用するのが一
般的であるが、これらにおいては、包装材料のラミネー
ト加工条件の設定がが難しく、高価格であるだけでなく
、透気度を自由に調整する事は不可能であった。Conventional oxygen scavenger packages using microporous membranes or nonwoven fabrics generally use packaging materials in which a microporous membrane or nonwoven fabric is laminated with a perforated low-melting-point sealant film. In these cases, it is difficult to set the laminating processing conditions for the packaging material, which is not only expensive, but also makes it impossible to freely adjust the air permeability.
一方、 本発明においては(A)と(B)とをヒートシ
ールにて貼り合わせたラミネートフィルムの(B)を接
着層としていることから包装材料の製造条件の設定が容
易であるばかりでなく、その透気度を自由に調節するこ
とができる。On the other hand, in the present invention, since (B) of the laminate film made by pasting (A) and (B) together by heat sealing is used as an adhesive layer, it is not only easy to set the manufacturing conditions of the packaging material, but also Its air permeability can be adjusted freely.
また、このようにして形成されたラミネートフィルムは
、包装材料の補強、透気度の調節と共に、製袋する際の
シール層としても機能する。Furthermore, the laminate film thus formed functions not only to reinforce the packaging material and adjust air permeability, but also as a sealing layer during bag making.
特に、有孔の低融点のシーラントフィルムをラミネート
した場合は、透気度の調整が難しいが本発明の微多孔膜
(B)では、微細孔がフィルムの全面に均一に分布して
いるのでヒートシール後も微細孔が保持されるので、十
分な透気性が保持される。In particular, when laminating a porous, low-melting point sealant film, it is difficult to adjust the air permeability, but with the microporous membrane (B) of the present invention, the micropores are uniformly distributed over the entire surface of the film, so it is difficult to adjust the air permeability. Since the fine pores are maintained even after sealing, sufficient air permeability is maintained.
更に、本発明においては、不織布、微多孔膜もしくは、
耐水耐油性加工紙を用いた包装材料を用いることにより
、不織布、微多孔膜もしくは、耐水耐油性加工紙の特徴
がそのまま生かされ、更に(B)が接着層と包装材料の
補強材としての働きを併せ持つことから、その接着強度
と製袋性およびフィルムのフレキシビリティに起因する
使い易さは、フィルムの厚みを調整する事で制御可能で
ある。Furthermore, in the present invention, a nonwoven fabric, a microporous membrane, or
By using packaging materials made of water- and oil-resistant treated paper, the characteristics of non-woven fabric, microporous membranes, or water- and oil-resistant treated paper can be utilized as is, and (B) can also serve as an adhesive layer and reinforcing material for the packaging material. Therefore, the adhesive strength, bag-forming properties, and ease of use due to the flexibility of the film can be controlled by adjusting the thickness of the film.
その結果、不織布、微多孔膜もしくは耐水耐油性加工紙
が、本来、有している透気度を大巾に低下することなく
安定した透気度を付与する事ができるため、脱酸素剤包
装体は安定した脱酸素性能を発揮する事ができ、同時に
好適な製袋性と十分な接着強度を持った脱酸素剤包装体
が得られる。As a result, nonwoven fabrics, microporous membranes, or water- and oil-resistant treated papers can be given stable air permeability without significantly reducing their original air permeability, making it possible to package oxygen absorbers. The body can exhibit stable oxygen scavenging performance, and at the same time, an oxygen scavenger package can be obtained that has suitable bag-forming properties and sufficient adhesive strength.
本発明は、安定した脱酸素性能を有し、かつ耐水性、耐
油性、耐アルコール性に優れた脱酸素剤包装体を提供す
るものであり、その食品保存分野を始めとする産業上の
意義は極めて大きい。The present invention provides an oxygen scavenger package that has stable oxygen scavenging performance and is excellent in water resistance, oil resistance, and alcohol resistance, and has industrial significance including the food preservation field. is extremely large.
第1図Figure 1
第1図:不織布、微多孔膜もしくは耐水耐油性加工紙に
微多孔膜を積層した本発明で使用する包装材料の実施態
様の断面図を示す。
第2図;同包装材料に脱酸素剤を充填して包装し、シー
ルした本発明の脱酸素剤包装体の実施態様の断面図を示
す。
第2図FIG. 1: A cross-sectional view of an embodiment of the packaging material used in the present invention, in which a microporous membrane is laminated on a nonwoven fabric, a microporous membrane, or a water- and oil-resistant treated paper. FIG. 2 is a sectional view of an embodiment of the oxygen absorber package of the present invention, in which the same packaging material is filled with an oxygen absorber, packaged, and sealed. Figure 2
Claims (1)
スチックフィルムおよび耐水耐油性加工紙よりなる群か
ら選ばれた1種の微細孔を有するフィルム(A)と(A
)と同等以下の軟化点を有する樹脂からなるガーレー式
透気度が0.1〜1,000秒/100mlの微多孔膜
(B)とを貼り合わせてなるガーレー式透気度が1〜1
0,000秒/100mlであるプラスチック積層フィ
ルム(C)からなる包装材料を脱酸素剤の包装材料の全
部もしくは一部として用い、該包装材料の(A)を外側
にして脱酸素剤を包装し、シールしたことを特徴とする
脱酸素剤用包装体(1) A film (A) with one type of microporous selected from the group consisting of a nonwoven fabric that does not pass water under normal pressure, a microporous plastic film, and a water- and oil-resistant treated paper;
) and a microporous membrane (B) with a Gurley air permeability of 0.1 to 1,000 seconds/100 ml made of a resin having a softening point equal to or lower than the Gurley air permeability of 1 to 1.
A packaging material made of a plastic laminated film (C) with a speed of 0,000 seconds/100ml is used as all or part of the packaging material for the oxygen absorber, and the oxygen absorber is packaged with (A) of the packaging material on the outside. A package for an oxygen absorber characterized by being sealed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34118789A JPH03200546A (en) | 1989-12-28 | 1989-12-28 | Package of oxygen absorbent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP34118789A JPH03200546A (en) | 1989-12-28 | 1989-12-28 | Package of oxygen absorbent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH03200546A true JPH03200546A (en) | 1991-09-02 |
Family
ID=18344037
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP34118789A Pending JPH03200546A (en) | 1989-12-28 | 1989-12-28 | Package of oxygen absorbent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03200546A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002002823A (en) * | 2000-06-26 | 2002-01-09 | Mitsubishi Gas Chem Co Inc | Oxygen absorber package and method for producing the same |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59142957A (en) * | 1983-01-28 | 1984-08-16 | 三菱瓦斯化学株式会社 | Deoxidizer package |
-
1989
- 1989-12-28 JP JP34118789A patent/JPH03200546A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59142957A (en) * | 1983-01-28 | 1984-08-16 | 三菱瓦斯化学株式会社 | Deoxidizer package |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002002823A (en) * | 2000-06-26 | 2002-01-09 | Mitsubishi Gas Chem Co Inc | Oxygen absorber package and method for producing the same |
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