JPH02166076A - Bag containing package - Google Patents
Bag containing packageInfo
- Publication number
- JPH02166076A JPH02166076A JP63308318A JP30831888A JPH02166076A JP H02166076 A JPH02166076 A JP H02166076A JP 63308318 A JP63308318 A JP 63308318A JP 30831888 A JP30831888 A JP 30831888A JP H02166076 A JPH02166076 A JP H02166076A
- Authority
- JP
- Japan
- Prior art keywords
- resin layer
- film
- polymer
- packaging
- heat
- 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
- 238000004806 packaging method and process Methods 0.000 claims abstract description 67
- 229920005989 resin Polymers 0.000 claims abstract description 52
- 239000011347 resin Substances 0.000 claims abstract description 52
- 239000011888 foil Substances 0.000 claims abstract description 31
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 30
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 26
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 239000002131 composite material Substances 0.000 claims abstract description 5
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 31
- 239000000805 composite resin Substances 0.000 claims description 8
- 239000002952 polymeric resin Substances 0.000 claims description 2
- 239000010410 layer Substances 0.000 abstract description 72
- 229920001577 copolymer Polymers 0.000 abstract description 11
- 150000001336 alkenes Chemical class 0.000 abstract description 6
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract description 4
- 238000003860 storage Methods 0.000 abstract description 4
- 239000000758 substrate Substances 0.000 abstract description 4
- 239000012790 adhesive layer Substances 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 28
- 238000007789 sealing Methods 0.000 description 15
- 239000000853 adhesive Substances 0.000 description 13
- 230000001070 adhesive effect Effects 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- 239000000126 substance Substances 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- -1 citric acid Chemical class 0.000 description 9
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 8
- 239000003973 paint Substances 0.000 description 8
- 229920001155 polypropylene Polymers 0.000 description 8
- 229920006015 heat resistant resin Polymers 0.000 description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 239000002985 plastic film Substances 0.000 description 5
- 229920006255 plastic film Polymers 0.000 description 5
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000009820 dry lamination Methods 0.000 description 4
- 239000001530 fumaric acid Substances 0.000 description 4
- 239000000976 ink Substances 0.000 description 4
- 238000010030 laminating Methods 0.000 description 4
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000014171 carbonated beverage Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 230000003628 erosive effect Effects 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
- 239000004299 sodium benzoate Substances 0.000 description 2
- 235000010234 sodium benzoate Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 235000019501 Lemon oil Nutrition 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000019502 Orange oil Nutrition 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004823 Reactive adhesive Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 210000004709 eyebrow Anatomy 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- 239000012793 heat-sealing layer Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000010501 lemon oil Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-N sodium;hydron;carbonate Chemical compound [Na+].OC(O)=O UIIMBOGNXHQVGW-UHFFFAOYSA-N 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Bag Frames (AREA)
- Package Specialized In Special Use (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は塗料、接着剤、印刷インキ、医薬、香粧品、食
品等の諸分野において有用な、直前に混合して使用すべ
き多成分系組成物の包装体において、任意の成分を含有
する該包装体中に5他の各成分を隔離して内蔵させるた
めの包装体内臓用包装袋に関するものである。Detailed Description of the Invention (Field of Industrial Application) The present invention is a multi-component system that is useful in various fields such as paints, adhesives, printing inks, pharmaceuticals, cosmetics, foods, etc., and which should be mixed immediately before use. The present invention relates to a packaging bag for internally containing a composition, which is used to separate and incorporate five other components into the package containing arbitrary components.
(従来の技術)
ポリウレタン塗料やエポキシ樹脂塗料のような二液型塗
料、エポキシ樹脂接着剤のような反応型接着剤、ウレタ
ン系フレキソ或いはグラビヤ・インキのような反応性印
刷インキ、二液型毛染め剤、重炭酸曹達等の重炭酸塩と
クエン酸等の有機酸とからなる発泡性炭酸飲料或いはそ
の発生ガスを利用する加圧噴霧容器などのように産業上
の諸分野において、少なくとも二成分からなっており使
用に当たって直前に混合する必要のある多成分系組成物
が種々存在する。通常、これらの組成物は各成分ごとに
個別に包装されており、使用毎に夫々の包装容器を開封
し、別の容器に移し替えるか、またはいづれか一つの成
分の容器に投入し、混合して使用されている。(Prior art) Two-component paints such as polyurethane paints and epoxy resin paints, reactive adhesives such as epoxy resin adhesives, reactive printing inks such as urethane-based flexo or gravure inks, two-component paints, etc. In various industrial fields, such as dyes, sparkling carbonated drinks made of bicarbonate such as bicarbonate soda and organic acids such as citric acid, and pressurized spray containers that utilize the generated gas, at least two components are used. There are various multi-component compositions that require mixing immediately before use. Usually, each component of these compositions is individually packaged, and each packaging container must be opened and transferred to another container or poured into a container for one of the components and mixed before each use. is used.
前記の混合作業において、各成分の移動や混合の際に内
容物が容器外に飛散したり、こぼれたりし易いため配合
比が変動して所期の効果が得られないことが屡々である
。In the above-mentioned mixing operation, the contents tend to scatter or spill out of the container when the components are moved or mixed, so the blending ratio often fluctuates and the desired effect cannot be obtained.
更に、容器外に内容物が散逸することにより周辺環境が
汚染され、皮膚などに付着するため不快であると共に汚
染部分が更に広がる結果となり、また衛生上の問題の発
生がある場合もある。Furthermore, the contents dissipate outside the container, contaminating the surrounding environment, and adhering to the skin, which is unpleasant and further spreads the contaminated area, which may also cause hygiene problems.
また、電子材料分野の接着剤、部分的な白髪染め、家庭
用塗料・接着剤、発泡性炭酸飲料など各成分を小量づつ
配合すればよい場合には、配合比率が不正確になり易い
上に損失が大きくなるという問題点がある。In addition, when it is necessary to mix small amounts of each component, such as adhesives for the electronic materials field, partial gray hair dye, household paints and adhesives, and sparkling carbonated drinks, the ratio of the ingredients is likely to be inaccurate. There is a problem that the loss becomes large.
その対策として使用直前に混合すべき多成分系組成物を
包装するための包装体において少なくとも任意の一成分
を含む該包装体中に、他の各成分を任意の個数の包装袋
に個別に収納して内蔵せしめ、使用に際して前記の内蔵
された包装袋を適当な手段によって破壊して内容物を混
合する方法が提案されている。As a countermeasure for this, in a package for packaging a multi-component composition to be mixed immediately before use, each of the other components is individually stored in an arbitrary number of packaging bags in the package containing at least one arbitrary component. A method has been proposed in which the packaging bag is built into the bag, and upon use, the built-in packaging bag is destroyed by appropriate means and the contents are mixed.
このような内蔵用包装袋としては食品、医薬品、化粧品
、トイレタリー用品等種々の用途分野において広く使用
されているアルミニウム箔とプラスチックフィルムとを
積層して得られる積層体を基材とする包装袋が包装加工
性、強度、ハンドリング性、光線遮蔽性、ガス遮断性、
耐水性、耐薬品性、耐熱性、耐寒性等諸物性のバランス
が良好であるため多く用いられている。Examples of such built-in packaging bags include packaging bags based on a laminate obtained by laminating aluminum foil and plastic film, which are widely used in various fields such as food, medicine, cosmetics, and toiletry products. Packaging processability, strength, handling properties, light shielding properties, gas barrier properties,
It is widely used because it has a good balance of physical properties such as water resistance, chemical resistance, heat resistance, and cold resistance.
これらの包装用基材はアルミニウム箔乃至はシートの一
方の表面に文字やデザイン等の印刷を施し、または施さ
ずに耐熱性の塗料で被覆するか、或いはポリエチレンテ
レフタレート、ポリカーボネート、ナイロンまたはポリ
プロピレン等のような耐熱性のプラスチックのフィルム
を接着させて耐熱性樹脂層とし、他方の表面には熱封緘
性のポリオレフィン樹脂層を設けた積層体が多く使用さ
れている。These packaging base materials are made by printing letters or designs on one surface of an aluminum foil or sheet, or coating them with a heat-resistant paint without printing, or by coating them with a heat-resistant paint such as polyethylene terephthalate, polycarbonate, nylon, or polypropylene. A laminate is often used in which a heat-resistant plastic film is bonded to form a heat-resistant resin layer, and a heat-sealable polyolefin resin layer is provided on the other surface.
包装体としての形態としては三方シール袋、四方シール
袋、ビロー包装、スティック包装、パウチ包装、ストリ
ップ包装等種々のものがあるが、いづれもこれらの積層
体の包装袋の内層となる熱封緘性樹脂層同志を対向面と
して、或いは熱封緘性樹脂層を包装袋の外層となる耐熱
性樹脂層の表面と重ね合わせ、所要部分を熱封緘するこ
とにより包装袋とする。There are various forms of packaging such as three-sided sealed bags, four-sided sealed bags, billow packaging, stick packaging, pouch packaging, and strip packaging, but all of these laminate packaging bags have heat-sealable properties that form the inner layer of the packaging bag. A packaging bag is obtained by placing the resin layers as opposing surfaces, or by overlapping the heat-sealable resin layer with the surface of the heat-resistant resin layer serving as the outer layer of the packaging bag, and heat-sealing the required portions.
そして、アルミニウム箔の表面に熱封緘性樹脂層として
ポリオレフィン樹脂フィルムを接着させ、他面に耐熱性
樹脂層として耐熱性プラスチックフィルムを貼着させる
場合に直接、加熱融着させることが一般に困難であるた
め、ウレタン系またはエポキシ系等の熱硬化性接着剤を
介して貼着する、所謂ドライラミネーション法が通常行
われている。When adhering a polyolefin resin film to the surface of aluminum foil as a heat-sealable resin layer and adhering a heat-resistant plastic film to the other surface as a heat-resistant resin layer, it is generally difficult to heat-seal the film directly. Therefore, a so-called dry lamination method, in which adhesives are attached using a thermosetting adhesive such as a urethane-based or an epoxy-based adhesive, is commonly used.
(発明が解決しようとする問題点)
前記したようにウレタン系接着剤によって熱封緘性フィ
ルムまたは耐熱性プラスチックフィルムとアルミニウム
箔乃至シートとを積層した従来の包装用熱封緘性積層体
は、眉間の接着力が優れており、諸物性が良好で、特に
耐熱性、耐水蒸気性に優れており、耐薬品性も良好であ
るため、レトルト食品用の包装材を始めとし、て種々の
分野に利ン用されている。(Problems to be Solved by the Invention) As described above, the conventional heat-sealable laminate for packaging in which a heat-sealable film or a heat-resistant plastic film and an aluminum foil or sheet are laminated with a urethane adhesive has a It has excellent adhesive strength and good physical properties, especially heat resistance, water vapor resistance, and chemical resistance, so it can be used in a variety of fields, including packaging materials for retort food. It is used for
しかしながら多成分系組成物の各成分の隔離包装を目的
とする包装体内蔵用包装袋として使用した場合には長期
の保存中に隔離保存された成分の混合が生じてくること
が多く問題となっている。However, when used as a packaging bag for internal packaging for the purpose of isolating and packaging each component of a multi-component composition, there are many problems such as mixing of the isolated components during long-term storage. ing.
このような組成物には染料、賦香や消臭のための香料、
防腐剤、殺菌剤、難燃剤、界面活性剤、反応のための触
媒、有機および無機の酸およびアルカリおよび有機溶剤
等浸透性や腐食性の大きい成分が添加されているのが普
通で、且つ隔離保存された成分は混合された組成物中よ
りも濃度が高くなるために侵食作用等が更に強くなるた
めに包装袋の損傷を来し易いためである。また、内蔵用
包装袋と言う特殊な保存環境のため製袋のデザインにか
かわらず包装袋の基材の断面は必ずいづれかの成分に接
触するため断面からの成分の浸透が生じる。従って前記
の熱封緘性フィルムおよび耐熱性プラスチックフィルム
または耐熱性被覆層とアルミニウム箔とを積層した包装
用熱封緘性積層体の各層を構成する材料は内外層を問わ
ず包装体の内容物に耐性を持つ必要があり、更に眉間に
用いる接着剤や表面の被覆剤にも同様の耐性が要求され
るのであるが、上記の条件を満たし多成分系組成物の各
成分の隔離包装を目的とする包装体内蔵用包装袋として
使用長期間に渉って保存に耐えるものは開発されていな
い。Such compositions include dyes, fragrances for fragrance and deodorization,
It is common for highly permeable and corrosive components such as preservatives, disinfectants, flame retardants, surfactants, catalysts for reactions, organic and inorganic acids and alkalis, and organic solvents to be added, and for isolation. This is because the stored components have a higher concentration than in the mixed composition, and therefore have a stronger erosive effect, which can easily damage the packaging bag. In addition, because of the special storage environment of a built-in packaging bag, the cross section of the base material of the packaging bag always comes into contact with some component, regardless of the design of the bag, so that components permeate through the cross section. Therefore, the materials constituting each layer of the heat-sealable laminate for packaging, which is made by laminating the heat-sealable film, heat-resistant plastic film, or heat-resistant coating layer and aluminum foil, are resistant to the contents of the package, regardless of whether they are the inner or outer layers. In addition, similar resistance is required for the adhesive used between the eyebrows and the surface coating material. No packaging bag has been developed that can be used and stored for a long period of time as a built-in packaging bag.
(問題点を解決するための手段)
本発明者等は、長期の保存において成分の侵食、浸透に
耐え、成分のの移動を阻止し得る多成分系組成物の各成
分の隔離包装を目的とする包装体内蔵用包装袋を得るこ
とを目的として研究を重ねた結果、アルミニウム箔の両
面にそれぞれカルボキシル基変性オレフィン(共)重合
体を主成分とする樹脂層(A)またはカルボキシル基変
性オレフィン(共)重合体を主成分とする樹脂層(A>
およびオレフィン(共)重合体を主成分とする樹脂層(
B)とからなる複合樹脂層(C)を、カルボキシル基変
性オレフィン(共)重合体樹脂層が接着剤層を介せずに
直接アルミニウム箔に接するように設けてなる複合材を
基材(D>として包装袋を製造することにより初期の目
的を達成し得ることを見出して本発明を完成したのであ
る。(Means for Solving the Problems) The present inventors have aimed at isolating and packaging each component of a multi-component composition that can withstand erosion and penetration of components during long-term storage and can prevent migration of components. As a result of repeated research with the aim of obtaining a packaging bag for internal use in packaging bodies, we found that resin layers (A) mainly composed of carboxyl group-modified olefin (co)polymers or carboxyl group-modified olefin (co)polymers were coated on both sides of aluminum foil. Co) Resin layer containing polymer as main component (A>
and a resin layer mainly composed of an olefin (co)polymer (
A composite resin layer (C) consisting of a base material (D The present invention was completed by discovering that the initial objective could be achieved by manufacturing a packaging bag as follows.
本発明の包装体内蔵用包装袋の基材(D>を構成する樹
脂層(A)の主成分であるカルボキシル基変性オレフィ
ン(共)重合体としてはオレフィン類特にエチレンまた
はプロピレンの(共)重合体のカルボキシル基変性体が
適当であり、室温において非粘着性フィルム形成性のも
のが好ましい。カルボキシル基は化学的に結合した形で
有するものが適当であり、その導入方法には特に制約は
ない。The carboxyl group-modified olefin (co)polymer which is the main component of the resin layer (A) constituting the base material (D>) of the packaging bag for built-in packaging of the present invention is a (co)polymer of olefins, particularly ethylene or propylene. A carboxyl group-modified product of the combination is suitable, and one that forms a non-adhesive film at room temperature is preferred.A carboxyl group having a chemically bonded form is suitable, and there are no particular restrictions on the method of introduction. .
Raち、(メタ)アクリル酸、クロトン酸、マレイン酸
1、フマル酸、イタコン酸及びシトラコン酸等の重合性
不飽和カルボン酸或いはそれらの無水物等をオレフィン
(共)重合体の製造時に共重合成分として共重合させる
方法或いはオレフィン(共)重合体にグラフト重合また
は他の不飽和重合性単量体と共にグラフと共重合させる
方法や無水マレイン酸、フマル酸またはイタコン酸等の
ジカルボン酸類をオレフィン(共)重合体に付加させる
方法等の常法を任意に選択することによりカルボキシル
基を導入することが出来る。また、例えば水酸基を有す
るオレフィン(共)重合体をマレイン酸。Rachi, polymerizable unsaturated carboxylic acids such as (meth)acrylic acid, crotonic acid, maleic acid 1, fumaric acid, itaconic acid, and citraconic acid, or their anhydrides, etc. are copolymerized during the production of olefin (co)polymers. A method in which dicarboxylic acids such as maleic anhydride, fumaric acid, or itaconic acid is copolymerized with an olefin (co)polymer as a component, or a method in which an olefin (co)polymer is graft polymerized or copolymerized with other unsaturated polymerizable monomers, and dicarboxylic acids such as maleic anhydride, fumaric acid, or itaconic acid are A carboxyl group can be introduced by arbitrarily selecting a conventional method such as addition to a co)polymer. In addition, for example, an olefin (co)polymer having a hydroxyl group is used as maleic acid.
フマル酸、イタコン酸等の多僅カルボン酸で半エステル
化することによってカルボキシル基を導入する方法等の
合成法を利用したものでもよい0才な、カルボキシル基
変性オレフィン(共)重合体はオレフィンおよびカルボ
キシル基変性単量体以外の他の変性用単量体が共重合さ
れていてもよい。The carboxyl group-modified olefin (co)polymer, which is 0 years old and may be one that utilizes a synthesis method such as a method of introducing a carboxyl group by half-esterification with a slightly carboxylic acid such as fumaric acid or itaconic acid, is an olefin and Modifying monomers other than the carboxyl group-modifying monomer may be copolymerized.
これらの(共)重合体は必要により単独或いは混合物と
して、または前記以外の(共)重合体類や樹脂類と混合
して使用される。These (co)polymers may be used alone or as a mixture, or mixed with other (co)polymers or resins, if necessary.
本発明の包装体内蔵用包装袋の基材(D>を構成する複
合樹脂層(C)の一方の層である樹脂層(B)の主成分
であるオレフィン(共)重合体としてはエチレンまたは
プロピレンの単独重合体および他のオレフィン類との共
重合体が好ましい、これらの(共)重合体類は分子量分
布、コンフォーメーションの相違等物理的構造の相異に
によっても諸物性が異なってくるが、本発明の方法にお
いてはいづれも使用可能である。好ましいポリオレフィ
ン(共)重合体としては種々の構造のポリエチレン、ポ
リプロピレン、ポリブテン−1、ポリ(4−メチルペン
テン−1)、エチレン−プロピレン共重合体、エチレン
・酢酸ビニル共重合体等であり、これらの〈共)重合体
も必要により単独或いは混合物として、または前記以外
の(共)重合体類や樹脂類と混合して使用される。Ethylene or Homopolymers of propylene and copolymers with other olefins are preferred; these (co)polymers have different physical properties due to differences in physical structure such as differences in molecular weight distribution and conformation. However, any of them can be used in the method of the present invention. Preferred polyolefin (co)polymers include polyethylene, polypropylene, polybutene-1, poly(4-methylpentene-1), and ethylene-propylene of various structures. Polymers, ethylene/vinyl acetate copolymers, etc., and these (co)polymers may be used alone or as a mixture, or mixed with (co)polymers or resins other than those mentioned above, if necessary.
各樹脂層(A)および(B)の厚さは各種め物性面から
は厚い方が好ましいが、経済性、加工性や取扱いの面か
らは必ずしも適当ではなく、数μ乃至100μ程度の範
囲にあればよく、特に制限はない。The thickness of each resin layer (A) and (B) is preferably thicker from the viewpoint of various physical properties, but it is not necessarily appropriate from the viewpoint of economy, processability and handling, and the thickness is in the range of several microns to about 100 microns. It's fine if you have one, and there are no particular restrictions.
本発明の方法において使用するアルミニウム箔は特に制
限はなく、一般に包装材として使用されるものであれば
よい、従って、必要により厚さは数μから数100μの
ものも使用され、また硬質及び軟質のいづれの箔も使用
できる。また、アルミニウム箔の表面には必要により文
字やデザインまたは着色皮膜を包装体の内容物に耐性の
ある被覆剤やインキを使用して8]刷等によって施すこ
とも可能である。The aluminum foil used in the method of the present invention is not particularly limited as long as it is generally used as a packaging material. Therefore, if necessary, aluminum foil with a thickness of several microns to several hundreds of microns may be used, and it may be hard or soft. You can also use any type of foil. Furthermore, it is also possible to apply letters, designs, or a colored film to the surface of the aluminum foil by printing or the like using a coating agent or ink that is resistant to the contents of the package, if necessary.
アルミニウム箔の表面にカルボキシル基変性オレフィン
(共)重合体を主成分とする樹脂層(A)またはカルボ
キシル基変性オレフィン(共)重合体を主成分とする樹
脂層(A>およびオレフィン(共〉重合体を主成分とす
る樹脂層(B)とからなる複合樹脂層(C)を、カルボ
キシル基変性オレフィン(共)重合体樹脂層が直接アル
ミニウム箔に接するように積層する方法としては押出し
ラミネート法によって各樹脂層をアルミニウム箔上に積
層する方法或いはT−ダイまたはインフレーション押出
機によってカルボキシル基変性オレフィン(共)重合体
を主成分とするvAD層(A>のフィルムおよびオレフ
ィン(共)重合体を主成分とする樹脂層(B)のフィル
ムを製造し、或いは共押出しによってカルボキシル基変
性オレフィン(共)重合体を主成分とする樹脂層<A)
およびオレフィン(共)重合体を主成分とする樹脂層(
B)とからなる複合樹脂層(C)のフィルムを製造し、
これらのフィルムをアルミニウム箔に熱融着させる方法
が適当である。いづれの場合においてもアルミニウム箔
とカルボキシル基変性オレフィン(共)重合体を主成分
とする樹脂層(A>とが接着するように積層する必要が
ある。A resin layer (A) mainly composed of a carboxyl group-modified olefin (co)polymer or a resin layer (A> and olefin (co)polymer) mainly composed of a carboxyl group-modified olefin (co)polymer is formed on the surface of the aluminum foil. A method of laminating a composite resin layer (C) consisting of a resin layer (B) whose main component is coalescence so that the carboxyl group-modified olefin (co)polymer resin layer is in direct contact with the aluminum foil is an extrusion lamination method. The vAD layer (A> film and the olefin (co)polymer as the main component) is formed by laminating each resin layer on aluminum foil or by using a T-die or an inflation extruder. A resin layer mainly composed of a carboxyl group-modified olefin (co)polymer is produced by manufacturing a film of the resin layer (B) as a component or by coextrusion <A)
and a resin layer mainly composed of an olefin (co)polymer (
B) Produce a film of composite resin layer (C) consisting of
A suitable method is to heat-seal these films to aluminum foil. In either case, it is necessary to laminate the aluminum foil and the resin layer (A>) whose main component is a carboxyl group-modified olefin (co)polymer so that they adhere to each other.
例えば複合樹脂J!1(C)のフィルムのカルボキシル
基変性オレフィン(共)重合体を主成分とする樹脂層(
A>とアルミニウム箔とを接触させ、前記カルボキシル
基変性オレフィン(共)重合体を主成分とする樹脂層(
A>のビカット軟化点以上の温度で軽く圧着して仮接着
させ、得られた積層体を前記ビカット軟化点以上の温度
の雰囲気中に保持した後、前記ビカット軟化点以上の温
度で圧着することによりカルボキシル基変性オレフィン
(共)重合体を主成分とする樹脂層(A>とアルミニウ
ム箔との強固な接着が得られる。For example, composite resin J! 1 (C) The resin layer (C) whose main component is a carboxyl group-modified olefin (co)polymer (
A> and aluminum foil are brought into contact with each other, and a resin layer containing the carboxyl-modified olefin (co)polymer as a main component
Temporarily bonding by lightly pressing at a temperature higher than the Vicat softening point of A>, holding the obtained laminate in an atmosphere at a temperature higher than the Vicat softening point, and then pressing at a temperature higher than the Vicat softening point. As a result, strong adhesion between the resin layer (A> mainly composed of a carboxyl group-modified olefin (co)polymer) and the aluminum foil can be obtained.
本発明の包装体内蔵用包装袋の製造においてはアルミニ
ウム箔の両面にそれぞれカルボキシル基変性オレフィン
(共〉重合体を主成分とする樹脂層(A)tたはカルボ
キシル基変性オレフィン(共)重合体を主成分とする樹
脂層(A)およびオレフィン(共)重合体を主成分とす
る樹脂層<8)とからなる複合樹脂層(C)を、カルボ
キシル基変性オレフィン(共)重合体樹脂層が直接アル
ミニウム箔に接するように設けてなる複合材を包装用基
材(D)とするが、封緘方法等の加工方法は通常の方法
で一般的な包装機械によって行なわれる。In manufacturing the packaging bag for built-in packaging of the present invention, a resin layer (A) containing a carboxyl group-modified olefin (co)polymer or a carboxyl group-modified olefin (co)polymer is applied on both sides of the aluminum foil. A composite resin layer (C) consisting of a resin layer (A) mainly composed of and a resin layer <8) mainly composed of an olefin (co)polymer, is The composite material provided so as to be in direct contact with the aluminum foil is used as the packaging base material (D), and processing methods such as sealing are carried out in a conventional manner using a general packaging machine.
(作用および効果)
本発明の包装体内蔵用包装袋の基材(D)を構成する樹
脂層(A)の主成分であるカルボキシル基変性オレフィ
ン(共)重合体は特にアルミニウム箔に対する接着性に
寄与するものであり、各種の有機、無機の薬品に対する
活性が小さく種々の分野に於ける包装体の主要内容物や
添加剤、例えば染料、顔料、香料、防腐剤、防薇剤、殺
菌網、難燃剤、界面活性剤、触媒、有機および無機の酸
およびアルカリに対しても侵され難いため、包装袋の基
材(D>の外面の表面層ととしても適当であるがアルミ
ニウム箔やオレフィン系プラスチックに対する熱封緘性
に優れているので内面の熱封緘性樹脂層として使用する
と効果が大きい。(Functions and Effects) The carboxyl group-modified olefin (co)polymer, which is the main component of the resin layer (A) constituting the base material (D) of the packaging bag for built-in packaging of the present invention, has particularly good adhesiveness to aluminum foil. It has low activity against various organic and inorganic chemicals, and is used as the main contents and additives of packaging in various fields, such as dyes, pigments, fragrances, preservatives, preservatives, sterilizing nets, etc. Because it is resistant to flame retardants, surfactants, catalysts, organic and inorganic acids and alkalis, it is also suitable as the outer surface layer of the packaging bag base material (D>), but aluminum foil and olefin-based Since it has excellent heat-sealability for plastics, it is highly effective when used as a heat-sealable resin layer on the inner surface.
本発明の包装体内蔵用包装袋の基材(D)を構成する複
合樹脂層(C)の一方の樹脂層(B)の主成分であるオ
レフィン(共〉重合体は前記各種分野に於ける包装袋の
主要内容物や添加剤に対する抵抗性が非常に大きく、物
理的構造や共重合に於ける共単量体の種類や配合量の選
択により熱封緘性を示す樹脂層や耐熱性樹脂層とするこ
とが出来る。従ってカルボキシル基変性オレフィン(共
)重合体を主成分とする樹脂層(A)の上に積層してオ
レフィン系(共)重合体を主成分とする耐熱性樹脂層と
したり、或いは耐熱性樹脂層に対する熱封緘層とするこ
とが出来る。The olefin (co)polymer which is the main component of one resin layer (B) of the composite resin layer (C) constituting the base material (D) of the packaging bag for built-in packaging of the present invention is used in the various fields mentioned above. A resin layer or heat-resistant resin layer that has extremely high resistance to the main contents of the packaging bag and additives, and exhibits heat sealability depending on the physical structure and selection of the type and amount of comonomer in copolymerization. Therefore, it can be laminated on the resin layer (A) whose main component is a carboxyl group-modified olefin (co)polymer to form a heat-resistant resin layer whose main component is an olefin (co)polymer. Alternatively, it can be used as a heat sealing layer for a heat-resistant resin layer.
本発明の包装体内蔵用包装袋の基材(D>はいづれかの
面の樹脂層を熱封緘性とすることにより熱封緘によって
包装袋に加工することが出来、基材(D>を構成する樹
脂層およびアルミニウム箔の各層間は直接接着している
ため包装体内容物による基材断面からの侵食や破壊が生
じない。The base material (D> of the packaging bag for built-in packaging of the present invention can be processed into a packaging bag by heat sealing by making the resin layer on either side heat sealable. Since the resin layer and the aluminum foil are directly bonded to each other, the cross section of the base material is not eroded or destroyed by the contents of the package.
以下、実施例によって更に詳細に説明する。Hereinafter, the present invention will be explained in more detail with reference to examples.
[実施例1]
フィルム1(樹脂層(A>のフィルム)の製造:アドマ
ーNEO70(三井石油化学工業圏製カルボキシル基変
性線状低密度ポリエチレン;ビカット軟化点87℃、メ
ルトインデックス1.0)のベレットから、インフレー
ションフィルム押出成形機を使用してシリンダー温度1
60℃、ダイス温度197°Cで厚さ30μのフィルム
を製造した。[Example 1] Production of film 1 (resin layer (A> film): Admer NEO70 (carboxyl group-modified linear low density polyethylene manufactured by Mitsui Petrochemical Industries; Vicat softening point 87°C, melt index 1.0) From the pellet, cylinder temperature 1 using a blown film extruder
A film with a thickness of 30μ was produced at 60°C and a die temperature of 197°C.
フィルム2(樹脂層(C)のフィルム)の製造:樹脂層
(A)の成分としてフィルム1の例に記載したアトマー
NEO70を使用し、樹脂層(B)の成分としてUPポ
リプロFM201−F(ユニオンポリマm−製ポリプロ
ピレン;ビカット軟化点135℃、メルトインデックス
8.0)を使用して二層インフレーション押出成形機を
使用してシリンダー温度165℃、ダイス温度200℃
でフィルムを製造した。得られた複合樹脂層(C)のフ
ィルムの厚さは40μで、樹脂層(A)および(B)の
厚さはそれぞれ20μとした。Production of film 2 (film of resin layer (C)): Atomer NEO70 described in the example of film 1 was used as a component of the resin layer (A), and UP Polypro FM201-F (Union) was used as a component of the resin layer (B). Polymer M-made polypropylene (Vicat softening point 135°C, melt index 8.0) was used using a two-layer inflation extruder with a cylinder temperature of 165°C and a die temperature of 200°C.
The film was produced. The film thickness of the obtained composite resin layer (C) was 40 μm, and the thicknesses of the resin layers (A) and (B) were each 20 μm.
包装用基材(Dl)の製、遣:
厚さ20μの軟質アルミニウム箔の一面にフィルム2の
樹脂層(A)側を接触させて、170℃に設定したスチ
ール製加熱ロールとシリコーンゴム製圧桐とからなるプ
レスロールにより4 Kg/+仮接着させた後、雰囲気
温度170°Cの加熱炉中に10秒間保持し、更に前記
と同条件に設定したプレスロールで圧着して積層した。Preparation and use of the packaging base material (Dl): The resin layer (A) side of the film 2 was brought into contact with one side of a soft aluminum foil having a thickness of 20μ, and a steel heating roll set at 170°C and a silicone rubber pressure roller were used. After temporary adhesion of 4 kg/+ using a press roll made of paulownia wood, the pieces were held in a heating furnace at an ambient temperature of 170°C for 10 seconds, and then pressed and laminated using a press roll set under the same conditions as above.
次に、上記積層体のアルミニウム箔の他面にフィルム1
を前記のフィルム2の積層作業と同様にして積層し、目
的の包装用基材(Dl)を得た。Next, a film 1 is placed on the other side of the aluminum foil of the laminate.
were laminated in the same manner as the lamination process for film 2, to obtain the desired packaging base material (Dl).
熱封緘強度試験:
得られた包装用基材(Dl)をそれぞれフィルム1同士
およびフィルム1面とフィルム2面とを圧力3 Kg/
cm2で1秒間の条件で180℃で熱封緘を行なった。Heat sealing strength test: The obtained packaging base material (Dl) was applied to each film 1 and the film 1 side and the film 2 side at a pressure of 3 kg/
Heat sealing was performed at 180° C. for 1 second at cm2.
これらの試料の180度剥離強度の剥離速度200 m
/sin、において測定したが、フィルム1面間士の場
合は熱封緘強度が大で2000g。Peel speed of 180 degree peel strength of these samples is 200 m
/sin, the heat sealing strength was as high as 2000 g in the case of one side of the film.
を超えて基材破壊を生じた。フィルム1面と2面との場
合も1800g、で充分な熱封緘強度を示した。The base material was destroyed when the In the case of 1 side and 2 sides of the film, sufficient heat sealing strength was shown at 1800 g.
耐薬品性試験:
前記の熱封緘試験に供したものと同じ試料を使用し10
cn+X I Oc+*に裁断した包装用基材(Dl)
をフィルム1面が内面になるように円筒状にし、フィル
ム1面がフィルム2面に重なるように5m@巾で熱封緘
して円筒を作成した1円筒の両端は同様に5mm幅の熱
封緘によりフィルム1面間士の熱封緘部とし、ビロー包
装袋の構造にした。Chemical resistance test: Using the same sample as the one used in the heat sealing test above,
Packaging base material (Dl) cut into cn+X I Oc+*
Make it into a cylinder so that the first side of the film is the inner surface, and heat seal it with a width of 5 m so that the first side of the film overlaps the second side of the film to create a cylinder. Both ends of the cylinder are similarly heat sealed with a width of 5 mm. The heat-sealed part was made between one side of the film, and the structure was made into a billow packaging bag.
このとロー包装袋にはそれぞれ10%塩酸、10苛性曹
達、メタノール、60zエタノール、トルエン、メチル
エチルケトン、酢酸エチル、ρ−トルエンスルホン酸(
5%キシレン/ブタノール溶液)、オレンジ油、レモン
油、安息香酸ナトリウム(5%水溶液)、ラウリル酸ナ
トリウム(2%水溶液)、中性界面活性剤(ノニルフェ
ノール型、HLB=17.10%水溶液)の薬液を予め
封入し、さらに封入したものと同一の薬液中に中に浸漬
し、40℃で3ヶ月間放置後、包装用基材(D)および
その熱封緘部分の状態を観察した。This and the raw packaging bag each contain 10% hydrochloric acid, 10% caustic soda, methanol, 60z ethanol, toluene, methyl ethyl ketone, ethyl acetate, ρ-toluenesulfonic acid (
5% xylene/butanol solution), orange oil, lemon oil, sodium benzoate (5% aqueous solution), sodium laurate (2% aqueous solution), neutral surfactant (nonylphenol type, HLB = 17.10% aqueous solution). A chemical solution was sealed in advance, and the package was immersed in the same chemical solution as the sealed one, and after being left at 40° C. for 3 months, the state of the packaging base material (D) and its heat-sealed portion was observed.
包装用基材の各層および熱封緘部分の表面乃至界面に明
確な変化は観察されず、眉間の接着が保持されていた。No clear changes were observed in the surfaces or interfaces of each layer of the packaging base material and the heat-sealed portion, and the glabella adhesion was maintained.
(比較例1]
フィルム2°の製造:
樹脂層(C)として実施例1で使用したUPポリプロF
M201−F(ユニオンポリマー−製ポリプロピレン;
ビカット軟化点135℃、メルトインデックス8.0)
の単層フィルムをインフレーション押出成形機によりシ
リンダー温度165℃、ダイス温度200℃で製造した
。得られたフィルムの厚さは20μとした。(Comparative Example 1) Production of film 2°: UP Polypro F used in Example 1 as the resin layer (C)
M201-F (polypropylene manufactured by Union Polymer;
Vicat softening point 135℃, melt index 8.0)
A single-layer film was produced using an inflation extruder at a cylinder temperature of 165°C and a die temperature of 200°C. The thickness of the obtained film was 20μ.
包装用基材(D 1′)の製造:
実施例1において使用した同様のアルミニウム箔の一面
に前記フィルム2°を二液性ポリウレタン系のドライラ
ミネーション用接着剤(大田薬品工業■製、タケラック
A310/タケネートA3)を使用して通常の工程によ
り積層した。Production of packaging base material (D1'): The above film 2° was coated on one side of the same aluminum foil used in Example 1 with a two-component polyurethane dry lamination adhesive (manufactured by Ota Pharmaceutical Co., Ltd., Takelac A310). /Takenate A3) and laminated by a normal process.
次に、上記積層体のアルミニウム箔の他面に実施例1の
フィルム1を前記フィルム2′と同様にドライラミネー
ション用接着剤を使用して積層し、包装用基材(DIo
)を得た。Next, the film 1 of Example 1 was laminated on the other side of the aluminum foil of the laminate using a dry lamination adhesive in the same manner as the film 2', and the packaging base material (DIo
) was obtained.
熱封緘強度試験
得られた包装用基材(D 1”〉をそれぞれフィルム1
面同士およびフィルム1面とフィルム2゛面とを実施例
1と同機にして行なった。これらの試料の180度剥離
強度の剥離速度200 m/sin、において測定した
が、フィルム1面間士の場合は熱封緘強度が大で200
0 g、を超えて基材破壊を生じ、フィルム1面と2°
面との場合も1960g、と大きい値を示した。Heat sealing strength test The obtained packaging base material (D 1”) was
The test was carried out using the same machine as in Example 1, with both sides and the first side of the film and the second side of the film being used. The 180 degree peel strength of these samples was measured at a peel rate of 200 m/sin, but in the case of films with one side to the other, the heat sealing strength was 200 m/sin.
If the weight exceeds 0 g, the base material will be destroyed, and the film will be
The case with the surface also showed a large value of 1960g.
耐薬品性試験:
前記の熱封緘試験に供した同じ試料を使用して実施例1
におけると同様にしてビロー包装袋を作成し、同様に耐
薬品性試験を行なった。Chemical resistance test: Example 1 using the same sample subjected to the heat sealing test above.
A billow packaging bag was prepared in the same manner as in , and a chemical resistance test was conducted in the same manner.
アルミニウム箔打よびフィルム1と2°は大きな変化は
認められなかったがドライラミネーション用接着剤層は
安息香酸ナトリウム以外の薬液中に浸漬した場合は接着
強度をまったく失っているか、または剥離を生じていた
。No major changes were observed for aluminum foil stamping and films 1 and 2°, but the adhesive layer for dry lamination lost all adhesive strength or peeled when immersed in chemicals other than sodium benzoate. Ta.
[実施例2]
フィルム3(樹脂層<A)のフィルム)の製造:アドマ
ーQEO50(三井石油化学工業■製カルボキシル基変
性ポリプロピレン;ビカット軟化点120℃、メルトイ
ンデックス27.0 >のベレットから、実施例1にお
けるフィルム1の製造と同様にしてインフレーションフ
ィルム押出成形機を使用して厚さ30μのフィルムを製
造した。[Example 2] Production of film 3 (film of resin layer <A): Performed from a pellet of Admar QEO50 (carboxyl group-modified polypropylene manufactured by Mitsui Petrochemical Industries, Ltd.; Vicat softening point: 120°C, melt index: 27.0) A 30 micron thick film was produced using a blown film extruder in the same manner as in the production of Film 1 in Example 1.
包装用基材(D2)の製造:
厚さ20μの軟質アルミニウム箔の一面に実施例1のフ
ィルム2の樹脂層(A>!Mを実施例1と同様に処理し
てプレスロールで圧着、積層した。Manufacture of packaging base material (D2): The resin layer (A>!M) of film 2 of Example 1 was treated in the same manner as in Example 1, and the resin layer (A>!M) of the film 2 of Example 1 was treated in the same manner as in Example 1, and then pressed and laminated with a press roll. did.
次に、上記積層体のアルミニウム箔の他面に前記フィル
ム3を前記のフィルム2の積層作業と同機にして積層し
、目的の包装用基材(D2)を得た。Next, the film 3 was laminated on the other side of the aluminum foil of the laminate using the same machine as the film 2, to obtain the desired packaging base material (D2).
熱封緘強度試@:
得られた包装用基材(D2)をそれぞれフィルム1面間
士およびフィルム1面とフィルム2面とを圧力3にg/
cm2で1秒間の条件で180℃で熱封緘を行なった。Heat sealing strength test @: The obtained packaging base material (D2) was applied to a pressure of 3 g /
Heat sealing was performed at 180° C. for 1 second at cm2.
これらの試料の180度剥離強度の剥離速度200 m
/sin、において測定したが、フィルム1面間士の場
合は熱封緘強度が大で2000g、を超えて基材破壊を
生じた。フィルム1面と2面との場合も2000g、を
超えて基材破壊を生じた。Peel speed of 180 degree peel strength of these samples is 200 m
/sin, and in the case of one side of the film, the heat sealing strength was high and exceeded 2000 g, causing destruction of the base material. In the case of the first and second sides of the film, the weight exceeded 2000g, causing substrate failure.
耐薬品性試験:
前記の熱封緘試験に供したものと同じ試料を実施例1と
同機にそれぞれの薬液によって耐薬品性試験を行なった
。Chemical resistance test: A chemical resistance test was conducted using the same sample as that used in the heat sealing test described above using each chemical solution on the same machine as in Example 1.
包装用基材の各層および熱封緘部分の表面乃至界面に明
確な変化は観察されず、層間の接着が保持されていた。No clear changes were observed in the surfaces or interfaces of each layer of the packaging base material and the heat-sealed portion, and adhesion between the layers was maintained.
Claims (1)
レフィン(共)重合体を主成分とする樹脂層(A)また
はカルボキシル基変性オレフィン(共)重合体を主成分
とする樹脂層(A)およびオレフィン(共)重合体を主
成分とする樹脂層(B)とからなる複合樹脂層(C)を
、カルボキシル基変性オレフィン(共)重合体樹脂層が
直接アルミニウム箔に接するように設けてなる複合材を
包装用基材(D)として製造することを特徴とする、 使用時に混合するべき多成分系組成物用の包装体におい
て、少なくとも一成分を収納した包装体の中に他成分を
収納して内蔵させるための内蔵用包装袋。[Scope of Claims] A resin layer (A) containing a carboxyl group-modified olefin (co)polymer as a main component or a resin layer (A) containing a carboxyl group-modified olefin (co)polymer as a main component on both sides of the aluminum foil, respectively. ) and a resin layer (B) containing an olefin (co)polymer as a main component, the composite resin layer (C) is provided such that the carboxyl group-modified olefin (co)polymer resin layer is in direct contact with the aluminum foil. A package for a multi-component composition to be mixed at the time of use, characterized in that a composite material consisting of: A built-in packaging bag for storing and incorporating.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63308318A JP2764208B2 (en) | 1988-12-06 | 1988-12-06 | Packaging bag for packaging |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63308318A JP2764208B2 (en) | 1988-12-06 | 1988-12-06 | Packaging bag for packaging |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02166076A true JPH02166076A (en) | 1990-06-26 |
| JP2764208B2 JP2764208B2 (en) | 1998-06-11 |
Family
ID=17979610
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63308318A Expired - Lifetime JP2764208B2 (en) | 1988-12-06 | 1988-12-06 | Packaging bag for packaging |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2764208B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09164184A (en) * | 1995-12-13 | 1997-06-24 | Nissho Corp | Infant beverage container |
| JP2012157589A (en) * | 2011-02-01 | 2012-08-23 | Ebisu Kagaku Kenkyusho:Kk | Extinction liquid medicine and simple fire extinguishing instrument filling the same |
| JP2014125229A (en) * | 2012-12-26 | 2014-07-07 | Daiwa Can Co Ltd | Container for microwave oven |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5744071U (en) * | 1980-08-25 | 1982-03-10 |
-
1988
- 1988-12-06 JP JP63308318A patent/JP2764208B2/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5744071U (en) * | 1980-08-25 | 1982-03-10 |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09164184A (en) * | 1995-12-13 | 1997-06-24 | Nissho Corp | Infant beverage container |
| JP2012157589A (en) * | 2011-02-01 | 2012-08-23 | Ebisu Kagaku Kenkyusho:Kk | Extinction liquid medicine and simple fire extinguishing instrument filling the same |
| JP2014125229A (en) * | 2012-12-26 | 2014-07-07 | Daiwa Can Co Ltd | Container for microwave oven |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2764208B2 (en) | 1998-06-11 |
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