JPH0358744A - Peeled apple package - Google Patents
Peeled apple packageInfo
- Publication number
- JPH0358744A JPH0358744A JP2081039A JP8103990A JPH0358744A JP H0358744 A JPH0358744 A JP H0358744A JP 2081039 A JP2081039 A JP 2081039A JP 8103990 A JP8103990 A JP 8103990A JP H0358744 A JPH0358744 A JP H0358744A
- Authority
- JP
- Japan
- Prior art keywords
- peeled
- apple
- package
- bag
- peeled apple
- 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
- 229920005989 resin Polymers 0.000 claims abstract description 26
- 239000011347 resin Substances 0.000 claims abstract description 26
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims abstract description 18
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 14
- 230000004888 barrier function Effects 0.000 claims abstract description 14
- 239000007864 aqueous solution Substances 0.000 claims abstract description 12
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000005977 Ethylene Substances 0.000 claims abstract description 10
- 239000001569 carbon dioxide Substances 0.000 claims abstract description 9
- 229910002092 carbon dioxide Inorganic materials 0.000 claims abstract description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims abstract description 8
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 8
- 239000000126 substance Substances 0.000 claims abstract description 8
- 239000002211 L-ascorbic acid Substances 0.000 claims abstract description 7
- 235000000069 L-ascorbic acid Nutrition 0.000 claims abstract description 7
- 238000007789 sealing Methods 0.000 claims abstract description 4
- 239000011780 sodium chloride Substances 0.000 claims abstract description 4
- 239000007789 gas Substances 0.000 claims description 27
- 150000002825 nitriles Chemical class 0.000 claims description 13
- 239000003755 preservative agent Substances 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000000178 monomer Substances 0.000 claims description 4
- 239000002250 absorbent Substances 0.000 abstract description 10
- 230000002745 absorbent Effects 0.000 abstract description 10
- -1 disoxidizer Substances 0.000 abstract description 8
- 239000000796 flavoring agent Substances 0.000 abstract description 5
- 235000019634 flavors Nutrition 0.000 abstract description 5
- 235000019640 taste Nutrition 0.000 abstract description 5
- 229920001542 oligosaccharide Polymers 0.000 abstract description 3
- 150000002482 oligosaccharides Chemical class 0.000 abstract description 3
- 229920000642 polymer Polymers 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 238000004321 preservation Methods 0.000 abstract 1
- 241000220225 Malus Species 0.000 description 35
- 235000021016 apples Nutrition 0.000 description 26
- 238000000034 method Methods 0.000 description 16
- 238000004519 manufacturing process Methods 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- 229940123973 Oxygen scavenger Drugs 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 239000005033 polyvinylidene chloride Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241000272470 Circus Species 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 235000011116 calcium hydroxide Nutrition 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 101100313164 Caenorhabditis elegans sea-1 gene Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 235000011850 desserts Nutrition 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 235000021178 picnic Nutrition 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000029058 respiratory gaseous exchange Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000002000 scavenging effect Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000011888 snacks Nutrition 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000019614 sour taste Nutrition 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Storage Of Fruits Or Vegetables (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野]
本発明は、ガスバリアー性樹脂からなる皮剥きリンゴ包
装体に関するものであり、詳しくは、保存性、食味およ
び風味保持性に優れた皮剥きリンゴ包装体に関するもの
である。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a peeled apple package made of a gas barrier resin, and more specifically, to a peeled apple package that has excellent preservability, taste, and flavor retention. This invention relates to an apple package.
リンゴは、食後のデザート、おやつまたはピクニック、
旅行の友として広く食されている。しかし、リンゴは皮
、芯をナイフ等で切る必要があり、そのまますぐに食べ
られるという手軽さに欠けていた。この要求に対して、
近年、皮および芯をあらかしめ取り除いた皮剥きリンゴ
が市販され始めた。しかしながら、これらの皮剥きリン
ゴは変色し易く、保存期間が短く、風味も損なわれやす
かった。そのため、脱酸素剤等を使用して包装すること
により皮剥きリンゴの保存期間の延長の研究がなされて
いるが、その効果は充分ではなかった。Apples are great for after-dinner desserts, snacks or picnics,
It is widely eaten as a travel companion. However, the skin and core of apples had to be cut with a knife, so they lacked the convenience of being able to be eaten immediately. For this request,
In recent years, peeled apples, in which the skin and core have been roughly removed, have become commercially available. However, these peeled apples were prone to discoloration, had a short shelf life, and were susceptible to loss of flavor. Therefore, research has been carried out to extend the shelf life of peeled apples by packaging them with oxygen absorbers, etc., but the effects have not been sufficient.
また完熟臭、水分、甘味等の風味および食味保持の問題
が未解決であった。In addition, the problems of ripe odor, moisture, flavor such as sweetness, and taste retention remain unsolved.
本発明の目的は従来の方法では不可能であった皮剥きリ
ンゴの保存期間を飛躍的に延長し、変色を防止し、風味
および食味保持性に優れ、歯応えも優れた皮剥きリンゴ
を保存ずる包装体を提供することにある。The purpose of the present invention is to dramatically extend the shelf life of peeled apples, which was impossible with conventional methods, and to preserve peeled apples that prevent discoloration, have excellent flavor and taste retention, and have excellent texture. The objective is to provide a package.
本発明者らは、かかる課題を解決する為鋭意検討し、皮
剥きリンゴを、特定のMi威からなる水溶液を用いて浸
漬処理し、該皮剥きリンゴの包装にガスバリアー性樹脂
を用い、且つ鮮度保持剤を内蔵して包装体内の特定のガ
スを特定量に維持する事により、この問題を解決し、遂
に本発明を完威した。The present inventors have made extensive studies to solve this problem, and have immersed peeled apples in an aqueous solution containing specific Mi, used a gas barrier resin to package the peeled apples, and This problem was solved by incorporating a freshness-preserving agent to maintain a specific amount of a specific gas within the package, and the present invention was finally brought to fruition.
すなわち、本発明は、皮剥きリンゴを、A.L−−アス
コルビン酸
B.塩化ナ1・リウム
C.保水性物質
からなる水溶液で処理し、該皮剥きリンゴをガスバリア
ー性樹脂からなる袋または容器に入れ、鮮度保持剤と共
に密j−J′8!ることを特徴とする皮剥きリンゴ包装
体である。That is, the present invention provides peeled apples with A. L--ascorbic acid B. Sodium chloride, Liumium C. The peeled apples are treated with an aqueous solution made of a water-retaining substance, placed in a bag or container made of gas barrier resin, and mixed with a freshness-preserving agent. This is a peeled apple package characterized by:
本発明で用いる皮?、リきリンゴは、その品種に制限は
ない。皮剥きリンゴは芯および皮の一部または全部を取
り除いたものが好ましい。The skin used in the present invention? There are no restrictions on the variety of Riki apples. Peeled apples are preferably those with the core and part or all of the skin removed.
本発明で用いるL−アスコルビン酸の量は水溶液中に、
0.1%〜5%が好ましい。さらに好ましくは0.5%
〜2%である。0.1%未満の場合はリンゴが変色し易
くなる。5%を越える場合は皮剥きリンコ゛にI,−ア
スコルビン酸臭が付き好ましくない。The amount of L-ascorbic acid used in the present invention is as follows:
0.1% to 5% is preferred. More preferably 0.5%
~2%. If it is less than 0.1%, apples are likely to discolor. If it exceeds 5%, the peeled apples will have an unfavorable odor of I,-ascorbic acid.
本発明で用いる塩化ナI・リウムの量は、水溶液中に0
.5%〜5%が好ましい。さらに好ましくは、1%〜3
%である。0.5%未満の場合はリンゴが変色し易くな
る。5%を越える場合は皮剥きリンゴが塩辛くなり好ま
しくない。The amount of sodium chloride/lium chloride used in the present invention is 0% in the aqueous solution.
.. 5% to 5% is preferred. More preferably, 1% to 3%
%. When it is less than 0.5%, apples tend to discolor. If it exceeds 5%, the peeled apple will become salty, which is not desirable.
本発明で用いる保水性物質としては、食品に用いられる
存機系の保水性物質であればいずれも使用できる。例と
して、糖アルコール類、オリゴ糖類等が挙げられる。As the water-retaining substance used in the present invention, any water-retaining substance used in foods can be used. Examples include sugar alcohols, oligosaccharides, and the like.
木発明で用いる保水性物質の量は、水溶液中に、1%〜
20%が好ましい。l%未満の場合は、皮剥きリンゴの
水分が蒸発し易く、パサっき易くなる。The amount of water-retentive substance used in wood invention is 1% to 1% in the aqueous solution.
20% is preferred. If it is less than 1%, the water in the peeled apple will easily evaporate and it will become dry.
20%を越えても良いが、コス1・アップとなるだけで
ある。It may be more than 20%, but it will only increase the cost by 1.
本発明における皮剥きリンゴの水溶液による処理時間は
、1分以」二である。1分未満の場合は、皮剥きリンゴ
が変色し易くなり好ましくない。The processing time of peeled apples with an aqueous solution in the present invention is 1 minute or more. If the time is less than 1 minute, the peeled apples tend to discolor, which is not preferable.
本発明で用いるガスバリアー性樹脂とは、高ニトリル系
樹脂、ポリ塩化ビニリデン、ポリビニルアルコール、エ
チレン−酢酸ビニル共重合体部分水和物等が挙げられる
。なかでも高ニトリル系樹脂が特に好ましく用いられる
。Examples of the gas barrier resin used in the present invention include high nitrile resins, polyvinylidene chloride, polyvinyl alcohol, and partially hydrated ethylene-vinyl acetate copolymer. Among them, high nitrile resins are particularly preferably used.
本発明で用いる高ニトリル系樹脂とは、アクリロニ1・
リル、メタクリロニI・リルなどの不飽和ニトリルを主
体とする共重合体であって不飽和ニトリル分を50重量
%以上含むものである。不飽和二1・リルと共重合可能
な単量体としては、スチレン、ブタジエン、イソブレン
、メチルアクリレート、エチルアクリレート、メチルメ
タクリレーI・、エチルメタアクリレートなどが挙げら
れこれらの1種または2種以Lを用いることができる。The high nitrile resin used in the present invention is acrylonitrile 1.
It is a copolymer mainly composed of unsaturated nitriles such as lyl and methacrylonitrile, and contains 50% by weight or more of unsaturated nitrile. Examples of monomers copolymerizable with unsaturated di-1-lyl include styrene, butadiene, isobrene, methyl acrylate, ethyl acrylate, methyl methacrylate I, and ethyl methacrylate. L can be used.
また、ブタジェン−アクリ口ニトリル共重合体、イソプ
レン−アクリロニトリル共重合体、ブタシエン−スチレ
ン共重合体、ポリブタジエン、ボリイソプレンなどのゴ
ム状重合体と不飽和二I・リルを主体とする共重合体と
の混合物、およびこれらのゴム状重合体の存在下に不飽
和二I・リルとIrI記共重合可能な単量体をグラフI
・重合させたものも用い得る。In addition, rubber-like polymers such as butadiene-acrylic nitrile copolymer, isoprene-acrylonitrile copolymer, butadiene-styrene copolymer, polybutadiene, polyisoprene, and copolymers mainly composed of unsaturated diI-lyl and Graph I shows the monomers copolymerizable with unsaturated DiI-Ryl and IrI in the presence of these rubbery polymers.
・Polymerized products can also be used.
上記樹脂をそれぞれ単独でフィルム及びシート化しても
よいし、他の樹脂と積層してもよい。Each of the above resins may be formed into a film or a sheet by itself, or may be laminated with other resins.
フィルム及びシート化は、押出威形法、カレンダー或形
法、インフレーション威形法等公知の方法で行うことが
できる。積層フィルム及び積層シー1・は公知の方法、
例えばドライラξネーション法、共押出法、接着法で得
ることができる。Films and sheets can be formed by known methods such as an extrusion forming method, a calender forming method, and an inflation forming method. The laminated film and laminated sheet 1. are prepared by a known method,
For example, it can be obtained by a dry lamination method, a coextrusion method, or an adhesion method.
本発明における袋および容器のl” ソブフィルム(蓋
)としては、ガスバリアー性の高い高ニトリル系樹脂の
単層フィルムあるいはボリブロピレン、ポリエチレン、
ポリエステル、ナイロンなどのフィルムに上記単層フィ
ルムを積層した多層フイルム、他のガスバリアー性樹脂
フイルムを積層した多層フィルム等が使用できる。袋の
場合、該フイルムを公知の方法により袋状ムこ製造され
る。トップフィルムの場合、該フィルムを通常のヒート
シル法、インバルスシール法などにより容器本体とシー
ルする。該フイルムは必要に応して印刷して包装体の商
品価値を高めることもできる。The l'' film (lid) of the bags and containers in the present invention may be a single layer film of high nitrile resin with high gas barrier properties, polypropylene, polyethylene, etc.
A multilayer film obtained by laminating the above-mentioned single layer film on a film of polyester, nylon, etc., a multilayer film obtained by laminating another gas barrier resin film, etc. can be used. In the case of a bag, the film is made into a bag-like bag by a known method. In the case of a top film, the film is sealed to the container body by a conventional heat seal method, invulsion seal method, or the like. The film can also be printed, if necessary, to increase the commercial value of the package.
本発明の袋およびトップフイルムの厚さは、所望のガス
ハリャー性により決定され、特に高ニトリル系樹脂の場
合は、不飽和ニトリル単量体の含有量により異なるが、
指標として通常、酸素透過度が20cc/ rd・at
m・2411r以下であるものが好ましい。The thickness of the bag and top film of the present invention is determined by the desired gas harrier properties, and particularly in the case of high nitrile resins, it varies depending on the content of unsaturated nitrile monomers, but
As an indicator, oxygen permeability is usually 20cc/rd・at
It is preferable that it is not more than m·2411r.
本発明の容器は、上記ガスバリアー性樹脂を通常の押出
し戒形法、カレンダー或形法、インフレーション戒形法
等により得られたシートを単層或いは積層して多層シー
トとし、真空或形、圧空或形することにより製造される
。高ニトリル系樹脂を使用する時は、容易に深絞りが可
能で、種々の形状、例えば円、四角、等の容器を得るこ
とが出来る。The container of the present invention is made of a single layer or a multilayer sheet obtained by laminating the above-mentioned gas barrier resin by a conventional extrusion molding method, calender molding method, inflation molding method, etc. Manufactured by shaping. When a high nitrile resin is used, deep drawing is easily possible, and containers of various shapes, such as circles and squares, can be obtained.
本発明の容器の壁の厚さは、所望のガスハリャー性の他
に内容量、必要強度等により変わるが、通常100〜8
00μmが好ましく、100μm未満では容器としての
剛性が不足するので好ましくない。The wall thickness of the container of the present invention varies depending on the desired gas harrier properties, internal capacity, required strength, etc., but is usually 100 to 8
00 μm is preferable, and less than 100 μm is not preferable because the container lacks rigidity.
また逆に800μmを越えても良いが作業性が不良とな
ったり、コストアンプになるだけである。On the other hand, it is possible to exceed 800 μm, but this will only result in poor workability and increase cost.
ポリ塩化ビニリデン、ポリビニルアルコール、エチレン
ー酢酸ビニル共重合体部分水和物等の樹脂を容器に用い
た場合、これらの樹脂単独では、容器或型、ヒートシー
ル等が行いにくいため、他の或型性、ヒートシール性に
優れた樹脂との多層構造とすることが必要となる。これ
らの多N構造物を容器形状に威型した場合、ハリャー層
が部分的に薄くなったり、バリャー切れ等の現象が起き
、内容物の保存性が低下し易くなることがあるため、あ
る程度厚さを持たせたり、形状等を考慮する必要がある
。When resins such as polyvinylidene chloride, polyvinyl alcohol, or ethylene-vinyl acetate copolymer partial hydrate are used for containers, it is difficult to shape the container, heat seal, etc. with these resins alone, , it is necessary to have a multilayer structure with a resin that has excellent heat sealability. When these multi-N structures are molded into a container shape, phenomena such as partially thinning of the barrier layer or breakage of the barrier may occur, which tends to reduce the shelf life of the contents. It is necessary to consider the shape, etc.
本発明における高ニトリル系樹脂を使用した場合は、加
工性、透明性、ヒートシール性に優れるため、単独で使
用でき、多層構造とする必要がない。また、威型による
ガスバリャー性の低下の恐れもない。When the high nitrile resin in the present invention is used, it has excellent processability, transparency, and heat sealability, so it can be used alone and does not need to have a multilayer structure. In addition, there is no fear that the gas barrier properties will deteriorate due to molding.
本発明で用いる鮮度保持剤としては、酸素、炭酸ガス、
エチレンガスを有効に吸収するものが使用できる。例と
して、脱酸素剤、炭酸ガス吸収剤、エチレンガス吸収剤
の単体の併用あるいは混合物が挙げられる。The freshness preserving agent used in the present invention includes oxygen, carbon dioxide,
A material that effectively absorbs ethylene gas can be used. Examples include a combination or a mixture of an oxygen scavenger, a carbon dioxide absorbent, and an ethylene gas absorbent.
本発明で用いる脱酸素剤としては、速効性のものならば
何れも使用できるが、好ましくは12時間以内に脱酸素
効果が現れるものである。例えば、鉄系、有機系のもの
が挙げられる。脱酸素剤は包装体内部の残存酸素量を密
封後12時間で0.1%以下とすることが好ましい。残
存酸素が0.1%を超える場合は、皮剥きリンゴの熟或
が進行しすぎ、酸味が生したり、品質の劣化、腐敗等が
起こりやすくなる。As the oxygen scavenger used in the present invention, any fast-acting one can be used, but preferably one that exhibits its oxygen scavenging effect within 12 hours. Examples include iron-based and organic-based materials. The oxygen absorber preferably reduces the amount of residual oxygen inside the package to 0.1% or less 12 hours after sealing. If the residual oxygen exceeds 0.1%, the ripening of the peeled apples will progress too much, resulting in a sour taste, deterioration of quality, spoilage, etc.
本発明で用いる炭酸ガス吸収剤としては、容器内部の炭
酸ガス量を1%未満に維持できるものであれば使用でき
る。例として、消石灰、アルカリ金属またはアルカリ土
類金属の水酸化物等が挙げられる。As the carbon dioxide absorbent used in the present invention, any material that can maintain the amount of carbon dioxide inside the container at less than 1% can be used. Examples include slaked lime, alkali metal or alkaline earth metal hydroxides, and the like.
本発明で用いるエチレンガス吸収剤としては、容器内部
のエチレンガス量を0.1ppm未満に維持できるもの
であれば使用できる。例として、大谷石等の多孔質鉱物
の粉末、ゼオライト、活性アルミナシリカ等が挙げられ
る。As the ethylene gas absorbent used in the present invention, any material that can maintain the amount of ethylene gas inside the container at less than 0.1 ppm can be used. Examples include porous mineral powder such as Oya stone, zeolite, activated alumina silica, and the like.
本発明で用いる鮮度保持剤としては、上記の脱酸素剤、
炭酸ガス吸収剤、エチレンガス吸収剤の他に、活性炭等
の多孔質の吸臭剤を併用して使用することもできる。The freshness preserving agent used in the present invention includes the above-mentioned oxygen scavenger,
In addition to the carbon dioxide gas absorbent and ethylene gas absorbent, a porous deodorant such as activated carbon can also be used in combination.
本発明では、皮剥きリンゴを前記水溶液で浸漬、水切り
後、鮮度保持剤と共に袋に内蔵し密封、または容器に内
蔵しトップフィルムにて密封ずる。In the present invention, peeled apples are immersed in the aqueous solution, drained, and then placed in a bag together with a freshness-preserving agent and sealed, or placed in a container and sealed with a top film.
[作用]
皮剥きリンゴを前記水溶液に浸漬、水切り後、袋または
容器に鮮度保持剤と共に収納する。皮剥きリンゴから発
生ずるエチレンガスは鮮度保持剤に速やかに吸収される
。また皮剥きリンゴは呼吸作用により酸素を消費し、炭
酸ガスを発生ずるが、この炭酸ガスも鮮度保持剤に速や
かCこ吸収される。[Operation] A peeled apple is immersed in the aqueous solution, drained, and then stored in a bag or container together with a freshness-preserving agent. Ethylene gas generated from peeled apples is quickly absorbed by the freshness preserving agent. Peeled apples also consume oxygen through respiration and generate carbon dioxide gas, which is quickly absorbed by the freshness-preserving agent.
よって、皮剥きリンゴはエチレンガス、炭酸ガスによる
品質の劣化、腐敗を防止することがごきる。Therefore, peeled apples can be prevented from deteriorating in quality and rotting due to ethylene gas and carbon dioxide gas.
以下、実施例により本発明を説明する。 The present invention will be explained below with reference to Examples.
製造例1
ブタジエン−アクリロニトリルゴム状其重合体(ブクジ
エン含量70重量%)10重量部の在在下でアクリロニ
トリル75重量部とメチルメタアクリレ−1−25重量
部を乳化重合して得た高二1・リル樹脂(アクリロニ1
・リル含量、約70重量%、窒素分析値による。)を用
いて、押出し或形法により厚み300μrnのシーl・
を得た。得られたシー1・を真空或形して1・レーを得
た。Production Example 1 Koji 1 was obtained by emulsion polymerization of 75 parts by weight of acrylonitrile and 1-25 parts by weight of methyl methacrylate in the presence of 10 parts by weight of a butadiene-acrylonitrile rubber-like polymer (butadiene content 70% by weight). Lil resin (acryloni 1)
- Lil content, approximately 70% by weight, based on nitrogen analysis value. ) to make a 300 μrn thick seal by extrusion or forming method.
I got it. The obtained sea 1. was vacuum-formed to obtain 1.re.
製造例2
製造例1ど同じ高ニトリル樹脂を用い、インフレーショ
ン戒形法により厚ノ40μmのフィルムを得た。Production Example 2 Using the same high nitrile resin as in Production Example 1, a film with a thickness of 40 μm was obtained by the inflation method.
製造例3 製造例2で得られたフィル1、を用いて袋を{7た。Manufacturing example 3 A bag was made using Fill 1 obtained in Production Example 2.
製造例4
製造例2で得られたフィル1、とボリゾロビレンフィル
1・どのラ案不−1・フィル1・を用いて袋を得た。Production Example 4 A bag was obtained using the fill 1 obtained in Production Example 2 and the polyzolobylene fill 1.
製造例5
エチレン−酢酸ビニル共重合体部分水和物とボリブロビ
レンフィルl1の多層フィルムヲ用いて袋を得た。Production Example 5 A bag was obtained using a multilayer film of partially hydrated ethylene-vinyl acetate copolymer and polypropylene film 11.
製造例6
ポリプロピレン、ポリ塩化ビニリデン、ポリエチレンの
多層フィルムを用いて袋を得た。Production Example 6 A bag was obtained using a multilayer film of polypropylene, polyvinylidene chloride, and polyethylene.
実施例1
皮および芯を除いたリンゴ(ふし)をL−アスコルビン
酸1重量%、食塩2重景%、保水性物質としてオリゴ糖
であるエスイー57(商品名、日研化学■製)7重量%
の水溶液に10分間浸漬、水切り後、製造例1で得られ
た1・レーに詰め、脱酸素剤として三菱瓦斯化学■製の
商品エージレスを収納し炭酸ガス吸収剤として消石灰、
エチレンガス吸収剤どして活性アルくナを収納し、製造
例2で得られたフィルムで熱シール封入し5゜Cで14
日間保々した。結果を第1表に示す。Example 1 An apple (Fushi) with its skin and core removed was mixed with 1% by weight of L-ascorbic acid, 2% by weight of salt, and 7% by weight of oligosaccharide SC57 (trade name, manufactured by Nikken Kagaku ■) as a water-retaining substance. %
After soaking in the aqueous solution for 10 minutes and draining the water, it was packed in the 1-ray obtained in Production Example 1, containing Ageless, a product manufactured by Mitsubishi Gas Chemical, as an oxygen scavenger, and slaked lime as a carbon dioxide absorbent.
Activated alkuna was stored as an ethylene gas absorbent, heat-sealed with the film obtained in Production Example 2, and heated at 5°C for 14 hours.
It lasted for days. The results are shown in Table 1.
実施例2
製造例3で得られた袋に詰める他は実施例1を繰り返し
た。結果を第1表に示す。Example 2 Example 1 was repeated except that the bags obtained in Production Example 3 were filled. The results are shown in Table 1.
実施例3
製造例4で得られた袋に詰める他は実施例1を繰返した
。結果を第1表に示す。Example 3 Example 1 was repeated except that the bags obtained in Preparation Example 4 were filled. The results are shown in Table 1.
実施例4
製造例5で得られた袋に詰める他は実施例1を繰返した
。結果を第1表に示す。Example 4 Example 1 was repeated except that the bags obtained in Preparation Example 5 were filled. The results are shown in Table 1.
実施例5
製造例6で得られた袋に詰める他は実施例1を繰返した
。結果を第l表に示す。Example 5 Example 1 was repeated except that the bags obtained in Preparation Example 6 were filled. The results are shown in Table I.
比較例1
水溶液処理しない他は実施例1を繰返した。結果を第1
表に示す。Comparative Example 1 Example 1 was repeated except that no aqueous solution treatment was performed. Results first
Shown in the table.
比較例2
L−アスコルビン酸6重量%とする他は実施例1を繰返
した。結果を第1表に示す。Comparative Example 2 Example 1 was repeated except that L-ascorbic acid was used at 6% by weight. The results are shown in Table 1.
比較例3
食塩をO.]重量%とずる他は実施例1を繰返した。結
果を第1表に示す。Comparative Example 3 Salt was added to O. ] Example 1 was repeated except for the weight percent. The results are shown in Table 1.
比較例4 食塩を7重量%とする他は実施例1を繰返した。Comparative example 4 Example 1 was repeated except that the salt content was 7% by weight.
結果を第1表に示す。The results are shown in Table 1.
比較例5
エスイー57を0.05重量%とずる他ば実施例Iを繰
返した。結果を第1表に示す。Comparative Example 5 Example I was repeated except that 0.05% by weight of SE 57 was added. The results are shown in Table 1.
本発明の皮剥きリンゴ包装体は極めて良好の保存性を具
有しており、かつ皮剥きリンゴの品質保持期間を飛躍的
に延長し、消費者に食味、香気も良好な皮剥きリンゴを
提供することが可能となり、皮剥きリンゴの流通販売に
寄与すること大である。The peeled apple package of the present invention has extremely good storage stability, dramatically extends the shelf life of peeled apples, and provides consumers with peeled apples that have good taste and aroma. This will greatly contribute to the distribution and sale of peeled apples.
第1表 (注〕 *印はL アスコルビン酸臭Table 1 (note〕 *mark is L ascorbic acid odor
Claims (1)
ー性樹脂からなる袋または容器に入れ、鮮度保持剤と共
に密封することを特徴とする皮剥きリンゴ包装体。 2、ガスバリアー性樹脂が50重量%以上の不飽和ニト
リル単量体を含有する高ニトリル系樹脂である請求項1
記載の皮剥きリンゴ包装体。 3、包装体内部の残存酸素量を密封後12時間で0.1
%以下、炭酸ガス量を1%未満、およびエチレンガス量
を0.1ppm未満に維持してなる請求項1記載の皮剥
きリンゴ包装体。[Claims] 1. Treating a peeled apple with an aqueous solution consisting of A, L-ascorbic acid B, sodium chloride C, and a water-retaining substance, and placing the peeled apple in a bag or container made of gas barrier resin. , a peeled apple package characterized in that it is sealed together with a freshness preserving agent. 2. Claim 1, wherein the gas barrier resin is a high nitrile resin containing 50% by weight or more of an unsaturated nitrile monomer.
The described peeled apple package. 3. The amount of residual oxygen inside the package was reduced to 0.1 within 12 hours after sealing.
%, the amount of carbon dioxide gas is maintained at less than 1%, and the amount of ethylene gas is maintained at less than 0.1 ppm.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8972389 | 1989-04-11 | ||
JP1-89723 | 1989-04-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0358744A true JPH0358744A (en) | 1991-03-13 |
Family
ID=13978685
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2081039A Pending JPH0358744A (en) | 1989-04-11 | 1990-03-30 | Peeled apple package |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0358744A (en) |
-
1990
- 1990-03-30 JP JP2081039A patent/JPH0358744A/en active Pending
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