JPH01281935A - Packaging material - Google Patents
Packaging materialInfo
- Publication number
- JPH01281935A JPH01281935A JP11150688A JP11150688A JPH01281935A JP H01281935 A JPH01281935 A JP H01281935A JP 11150688 A JP11150688 A JP 11150688A JP 11150688 A JP11150688 A JP 11150688A JP H01281935 A JPH01281935 A JP H01281935A
- Authority
- JP
- Japan
- Prior art keywords
- layer
- barrier properties
- oxygen gas
- resin layer
- gas barrier
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000005022 packaging material Substances 0.000 title claims abstract description 16
- 229920005989 resin Polymers 0.000 claims abstract description 27
- 239000011347 resin Substances 0.000 claims abstract description 27
- 239000010410 layer Substances 0.000 claims description 25
- 239000000853 adhesive Substances 0.000 claims description 17
- 230000001070 adhesive effect Effects 0.000 claims description 17
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 12
- 229910001882 dioxygen Inorganic materials 0.000 claims description 12
- 239000012790 adhesive layer Substances 0.000 claims description 10
- 239000011241 protective layer Substances 0.000 claims 1
- 239000007789 gas Substances 0.000 abstract description 23
- 230000004888 barrier function Effects 0.000 abstract description 22
- 238000000034 method Methods 0.000 abstract description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 5
- 239000001301 oxygen Substances 0.000 abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 abstract description 5
- 239000011342 resin composition Substances 0.000 abstract description 3
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 238000004806 packaging method and process Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000004230 Fast Yellow AB Substances 0.000 description 2
- 239000002386 air freshener Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 229920001342 Bakelite® Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000020997 lean meat Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 235000020995 raw meat Nutrition 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 235000020989 red meat Nutrition 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は必要に応してガス遮断性を除去することが可能
な透明性に優れた包装置A籾に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a packaging device A for paddy rice with excellent transparency, which allows gas barrier properties to be removed if necessary.
芳香剤、殺虫剤等のトイレタリー分野では、ガス遮断性
の低い包装材料が使用され製品寿命が短縮される問題や
、ガス遮断性の高い包装材料を使用することによる取扱
いの煩わしさやガス遮断性の高い包装材料と低い包装4
4オ′4の2種類の絹め合わせ等の方法、さらには実開
昭62−162024号公報のように和紙との組め合わ
せなどの方法が考えられたが、いずれもコストが高くな
る問題点や透明性の問題点があった。さらに食品分野で
は、牛肉の場合高いガス遮断慴包装側斜を使い、保存1
1を(寺たーUると、腐敗はしないが肉の赤身が酸素不
足のため枯色し商品価値が低下する問題があった。その
ためガス遮断性が必要′な時1υIが過ぎれば容易にガ
ス遮断性を低下させることのできる包装材料が望まれて
いた。In the toiletry field, such as air fresheners and pesticides, packaging materials with low gas barrier properties are used, resulting in shortened product lifespans, and the use of packaging materials with high gas barrier properties causes troublesome handling and problems with gas barrier properties. High packaging materials and low packaging 4
Methods such as combining two types of silk as shown in 4o'4, and methods such as combining with Japanese paper as in Japanese Utility Model Publication No. 62-162024 have been considered, but both methods have the problem of high cost. There were also issues with transparency. Furthermore, in the food industry, high gas barrier packaging is used for beef, and storage
1), there was a problem that although it did not spoil, the red meat would wither due to lack of oxygen and the product value would decrease.Therefore, when gas barrier properties are required, gas easily leaks after 1υI. Packaging materials that can reduce barrier properties have been desired.
〔発明が解決しようとする課題]
本発明は従来の包装材料では不可能であった透明性に優
れ、且つ安価でガス遮断性を容易に変えることが可能な
包装材r1を得んとして研究した結果、高いガス遮断性
の樹脂層と低いガス遮断性の樹脂層が容易に剥離できる
が、剥離する前の成形加工には耐えるような接着強度の
領域と接着層の組成に関する知見を得、さらに積層方法
についても検討を加えた結果本発明の完成に至ったもの
である。[Problems to be Solved by the Invention] The present invention was researched to obtain a packaging material r1 that has excellent transparency, which was impossible with conventional packaging materials, and which is inexpensive and whose gas barrier properties can be easily changed. As a result, we obtained knowledge about the composition of the adhesive layer and the region of adhesive strength where the resin layer with high gas barrier properties and the resin layer with low gas barrier properties can be easily peeled off, but can withstand molding processing before peeling. The present invention was completed as a result of consideration of the lamination method.
本発明は層構成が被包装物側から酸素ガス透過量が10
0cc/rrr ・2・24Hr・100 μm以上の
樹脂層(1)、樹脂層(1)又は樹脂(3)との接着強
度が20〜200 g / 25 mm巾の接着層(2
)、酸素ガス透過量が10cc/rK −2・24Hr
・1001tm以下の樹脂層(3)であることを特徴と
する包装材料及びその製造方法である。In the present invention, the layer structure has an oxygen gas permeation rate of 10% from the packaged object side.
0cc/rrr ・2・24Hr・100 μm or more resin layer (1), adhesive layer (2) with adhesive strength of 20 to 200 g / 25 mm width with resin layer (1) or resin (3)
), oxygen gas permeation rate is 10cc/rK -2・24Hr
- A packaging material characterized by a resin layer (3) of 1001 tm or less, and a method for producing the same.
本発明において用いられる低いガス遮断性の樹脂とは、
酸素ガス透過量が厚み100μmで100 cc/+f
・2・24Hr以上のものである。100cc/ni
・2・24Hr以下の酸素ガス透過量の樹脂ではガス遮
断性の樹脂層の除去後のガス透過量が不十分であり具体
的には、芳香剤の場合芳香が包装材料を透過して蒸発発
散されない。又、生肉包装では逆に酸素ガスが十分に透
過侵入できず肉の赤身の回復が遅れる。The low gas barrier resin used in the present invention is
Oxygen gas permeation rate is 100 cc/+f at a thickness of 100 μm
- 2.24 hours or more. 100cc/ni
- If the resin has an oxygen gas permeation rate of 2.24 hours or less, the gas permeation rate after removing the gas barrier resin layer will be insufficient. Specifically, in the case of air fresheners, the fragrance will permeate through the packaging material and evaporate. Not done. On the other hand, in raw meat packaging, oxygen gas cannot penetrate sufficiently and the recovery of lean meat is delayed.
酸素ガス透過量が100cc/+d ・2・24Hr・
100μm以上の樹脂としては、ポリオレフィン樹脂及
びその共重合体、ポリスチレン、ポリカーボネート、さ
らに軟質塩化ヒニル等である。又酸素ガス透過量を大き
くするために透明性を損なわない程度の充填剤等を先記
の樹脂を添加してもよい。Oxygen gas permeation amount is 100cc/+d・2・24Hr・
Examples of resins with a diameter of 100 μm or more include polyolefin resins and copolymers thereof, polystyrene, polycarbonate, and soft hinyl chloride. Further, in order to increase the amount of oxygen gas permeation, a filler or the like may be added to the above-mentioned resin to an extent that does not impair transparency.
又高いガス遮断性の樹脂として、酸素ガス透過量が厚み
100 μmで10cc/rrf ・2・24Hr以下
のものであり、エチレン・酢酸ビニル共重合体ケン化物
、ポリ塩化ビニリデン、ポリアミドさらにポリアクリロ
ニトリル等が使用できる。。In addition, as a resin with high gas barrier properties, the oxygen gas permeation rate is 10 cc/rrf ・2.24 Hr or less at a thickness of 100 μm, and it is suitable for saponified ethylene/vinyl acetate copolymer, polyvinylidene chloride, polyamide, and polyacrylonitrile. can be used. .
本発明の一実施例を図に示し説明する。第1図は本発明
の包装材料の一実施例の断面図であり1は高いガス遮断
性の樹脂層であり、3は低いガス遮断性の樹脂層である
。2は接着層であるがこの実施例では、層1に対して、
接着強度が低く抑えられており、層Iを剥離除去すると
第2図の様な断面図になる。An embodiment of the present invention will be described with reference to the drawings. FIG. 1 is a sectional view of one embodiment of the packaging material of the present invention, in which 1 is a resin layer with high gas barrier properties, and 3 is a resin layer with low gas barrier properties. 2 is an adhesive layer, but in this example, for layer 1,
The adhesive strength is kept low, and when layer I is peeled off, a cross-sectional view as shown in FIG. 2 is obtained.
接着層は、層1又は層3の一方し’v対して、接着強度
が20−200 g / 25 mm幅に制抑されてい
る必要がある。200 g / 2 S mm幅以上で
は剥離が容易でなく、又、4の剥離面が粗化され外観劣
化を起こす。The adhesive layer must have an adhesive strength of 20-200 g/25 mm width for either layer 1 or layer 3. If the width is 200 g/2 S mm or more, peeling is not easy, and the peeled surface of 4 becomes rough, causing deterioration in appearance.
一方接着強度が20 g / 25111111幅以下
ではフィルム加工時に容易tこ剥離現象が起こり、製品
にならない。On the other hand, if the adhesive strength is less than 20 g/25111111 width, peeling phenomenon will easily occur during film processing and the product will not be produced.
本発明では、接着層の接着強度が重要であり接着層の樹
脂組成は、接着する層l及び3の樹脂の種類によって決
められる。In the present invention, the adhesive strength of the adhesive layer is important, and the resin composition of the adhesive layer is determined by the types of resins in layers 1 and 3 to be adhered.
又、接着強度を充分に制抑するには、積層方法も考慮す
る必要がある。接着剤を使用するドライラミネート法で
は、接着強度を調整するための接着剤の調製が非常に困
難であるばかりでなく、そのような接着剤を使用しても
塗布する接着剤の厚みムラで全く、接着強度の制抑はで
きない。Furthermore, in order to sufficiently suppress the adhesive strength, it is necessary to consider the lamination method. In the dry lamination method that uses adhesives, not only is it extremely difficult to prepare the adhesive to adjust the adhesive strength, but even if such adhesives are used, the thickness of the applied adhesive is uneven, making it completely difficult to prepare the adhesive. , the adhesive strength cannot be suppressed.
又、熱プレス法では各樹脂層間の接着面への熱伝導が充
分でないため低い接着強度しか得られずバラツキも大き
くなる。又、加工コストが非常に高いものになる。In addition, in the hot press method, heat conduction to the bonding surfaces between each resin layer is insufficient, so only low bonding strength can be obtained and variations are large. Moreover, the processing cost becomes very high.
本発明では接着強度を制抑できる方法として検δ=t
Lだところ共押出法を用い、接着層の樹脂組成を選ぶご
とにより高い精度で制抑可能なことを見い出した。共押
出法では、完全に熔融した樹脂がシーテイングダイ内部
で一定の圧力下で積層され、押出されるため押出条件さ
え一定に制抑しておけば安定した接着強度が容易に得ら
れる。In the present invention, as a method for suppressing the adhesive strength, the test δ=t
Using a co-extrusion method, it was discovered that the adhesive layer could be suppressed with higher accuracy by selecting the resin composition of the adhesive layer. In the coextrusion method, completely melted resins are laminated under constant pressure inside a sheeting die and extruded, so stable adhesive strength can be easily obtained as long as the extrusion conditions are kept constant.
品いガス遮断性の樹脂(クラレ、エパールE105)と
低いガス遮断性の樹BF; (住友化学工業エバチー)
H2021F)を接着層(三井石油化学工業 エハフレ
ンクスP 2505 C)を中間にした構成で3層マル
チマニホールドダイを使って共押出した。Resin with high quality gas barrier properties (Kuraray, Epal E105) and wood BF with low gas barrier properties; (Sumitomo Chemical Everty)
H2021F) was coextruded using a three-layer multi-manifold die with an adhesive layer (Ehafrex P 2505 C, manufactured by Mitsui Petrochemical Industries, Ltd.) in the middle.
厚めはEI05”301!m /P2505C・301
1m/H2O21F・60μmの計120 μmであっ
た。エバールE105の層の剥離除去前後の酸素ガス透
過が及びエバー用2101層の剥離強度を測定したとこ
ろ次の様な結果であった。The thicker one is EI05”301!m /P2505C・301
The total length was 120 μm (1 m/H2O21F/60 μm). When the oxygen gas permeation of the EVAL E105 layer before and after peeling and removal and the peel strength of the EVAL 2101 layer were measured, the following results were obtained.
(1) 酸素ガス透過量
f剥離前 1・5°c/rK −2・24Hr■剥
離後 2200 cc / nイ・2・24Hr(
2) 剥離強度 1.05 g / 25 mm
幅〔発明の効果〕
本発明の包装材料及び製造方法に従うことにより、従来
得られなかった透明性に優れたガス遮断性を調整及び除
去可能な包装材料が得られ、トイレクリ−1食品分野で
広く利用できる。(1) Oxygen gas permeation rate f Before peeling 1・5°c/rK -2・24Hr ■After peeling 2200 cc/n I・2・24Hr (
2) Peel strength 1.05 g/25 mm
Width [Effect of the Invention] By following the packaging material and manufacturing method of the present invention, a packaging material with excellent transparency and gas barrier properties that can be adjusted and removed, which could not be obtained conventionally, can be obtained, and it is widely used in the toilet cleaner 1 food field. Available.
第1図は、本発明の包装材料の一実施例の断面図であり
、第2図は、高いガス遮断性の樹脂層を剥離除去した後
の断面図である。
特許出願人 住友ベークライト株式会社第1図FIG. 1 is a sectional view of one embodiment of the packaging material of the present invention, and FIG. 2 is a sectional view after the resin layer with high gas barrier properties has been peeled off and removed. Patent applicant Sumitomo Bakelite Co., Ltd. Figure 1
Claims (2)
cc/m^2・24Hr・100μm以上の樹脂層(1
)、樹脂層(1)又は樹脂層(3)との接着強度が20
〜200g/25mm幅の接着層(2)、酸素ガス透過
量が10cc/24Hr・100μm以下の樹脂層(3
)であることを特徴とする包装材料。(1) The layer structure has an oxygen gas permeation rate of 100 from the packaged object side.
cc/m^2・24Hr・100μm or more resin layer (1
), adhesive strength with resin layer (1) or resin layer (3) is 20
~200g/25mm width adhesive layer (2), oxygen gas permeation amount of 10cc/24Hr・100μm or less resin layer (3)
) A packaging material characterized by:
もうけた第(1)項記載の包装材料。(2) The packaging material according to item (1), further comprising a protective layer (4) on the outer surface of the resin layer (3).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63111506A JPH0647279B2 (en) | 1988-05-10 | 1988-05-10 | Packaging material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63111506A JPH0647279B2 (en) | 1988-05-10 | 1988-05-10 | Packaging material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01281935A true JPH01281935A (en) | 1989-11-13 |
JPH0647279B2 JPH0647279B2 (en) | 1994-06-22 |
Family
ID=14563035
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63111506A Expired - Lifetime JPH0647279B2 (en) | 1988-05-10 | 1988-05-10 | Packaging material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0647279B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5232767A (en) * | 1989-06-28 | 1993-08-03 | Kureha Kagaku Kogyo Kabushiki Kaisha | Heat-shrinkable laminate film |
JP2007283565A (en) * | 2006-04-14 | 2007-11-01 | Mitsubishi Plastics Ind Ltd | Gas barrier film, and packaging material and package using the film |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3925688A4 (en) | 2019-03-22 | 2022-11-02 | Murata Manufacturing Co., Ltd. | EMISSION CONTROL CATALYST AND EMISSION TREATMENT EQUIPMENT |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5363484A (en) * | 1976-11-18 | 1978-06-06 | Nippon Synthetic Chem Ind Co Ltd:The | Multilayer structure |
JPS5382880A (en) * | 1976-12-29 | 1978-07-21 | Mitsubishi Petrochemical Co | Method for making composite laminate improved gas barrier property |
JPS57175571A (en) * | 1981-04-20 | 1982-10-28 | Gunze Kk | Packing material for air emitting or air absorbing chemical material |
JPH0199624U (en) * | 1987-12-24 | 1989-07-04 |
-
1988
- 1988-05-10 JP JP63111506A patent/JPH0647279B2/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5363484A (en) * | 1976-11-18 | 1978-06-06 | Nippon Synthetic Chem Ind Co Ltd:The | Multilayer structure |
JPS5382880A (en) * | 1976-12-29 | 1978-07-21 | Mitsubishi Petrochemical Co | Method for making composite laminate improved gas barrier property |
JPS57175571A (en) * | 1981-04-20 | 1982-10-28 | Gunze Kk | Packing material for air emitting or air absorbing chemical material |
JPH0199624U (en) * | 1987-12-24 | 1989-07-04 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5232767A (en) * | 1989-06-28 | 1993-08-03 | Kureha Kagaku Kogyo Kabushiki Kaisha | Heat-shrinkable laminate film |
JP2007283565A (en) * | 2006-04-14 | 2007-11-01 | Mitsubishi Plastics Ind Ltd | Gas barrier film, and packaging material and package using the film |
Also Published As
Publication number | Publication date |
---|---|
JPH0647279B2 (en) | 1994-06-22 |
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