JPH0449035A - Heat-shrinkable film for packaging dry cell - Google Patents
Heat-shrinkable film for packaging dry cellInfo
- Publication number
- JPH0449035A JPH0449035A JP15833390A JP15833390A JPH0449035A JP H0449035 A JPH0449035 A JP H0449035A JP 15833390 A JP15833390 A JP 15833390A JP 15833390 A JP15833390 A JP 15833390A JP H0449035 A JPH0449035 A JP H0449035A
- Authority
- JP
- Japan
- Prior art keywords
- resin layer
- nylon
- copolymer
- film
- 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.)
- Pending
Links
- 238000004806 packaging method and process Methods 0.000 title claims abstract description 14
- 229920006257 Heat-shrinkable film Polymers 0.000 title claims description 9
- 239000004840 adhesive resin Substances 0.000 claims abstract description 12
- 229920006223 adhesive resin Polymers 0.000 claims abstract description 12
- 229920006122 polyamide resin Polymers 0.000 claims abstract description 9
- 229920013716 polyethylene resin Polymers 0.000 claims abstract description 8
- 229920001577 copolymer Polymers 0.000 abstract description 13
- 229920005989 resin Polymers 0.000 abstract description 10
- 239000011347 resin Substances 0.000 abstract description 10
- 229920005672 polyolefin resin Polymers 0.000 abstract description 6
- 150000001336 alkenes Chemical class 0.000 abstract description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 4
- 239000005977 Ethylene Substances 0.000 abstract description 4
- 239000004677 Nylon Substances 0.000 abstract description 4
- 229920001778 nylon Polymers 0.000 abstract description 4
- 229920000554 ionomer Polymers 0.000 abstract description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract description 3
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 abstract description 2
- 229920000299 Nylon 12 Polymers 0.000 abstract description 2
- 229920002292 Nylon 6 Polymers 0.000 abstract description 2
- 229920000305 Nylon 6,10 Polymers 0.000 abstract description 2
- 229920002302 Nylon 6,6 Polymers 0.000 abstract description 2
- 230000001070 adhesive effect Effects 0.000 abstract description 2
- 239000000178 monomer Substances 0.000 abstract description 2
- 238000010030 laminating Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 3
- 229920000092 linear low density polyethylene Polymers 0.000 description 3
- 239000004707 linear low-density polyethylene Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002184 metal Chemical class 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 150000003839 salts Chemical class 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〉
本発明は強度の優れた乾電池包装用熱収縮性フィルムに
関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a heat-shrinkable film for packaging dry batteries with excellent strength.
く従来の技術〉
従来より乾電池包装用の熱収縮性フィルムとしては各種
のものが散見され、特にポリ塩化ビニル製やポリエチレ
ン製のものが最も広く利用に供されている。ところが前
記ポリ塩化ビニル製のものはシール部の耐衝重性や落下
衝撃に対する強度が不足する傾向にあり、包装品の取扱
いに注意を要した。一方ポリエチレン製のものはシル強
度は満足するが融点が低いため熱収縮工程で溶融して穴
あきが生じ易く、こうした点で奸ましいとは云い得なか
った。BACKGROUND ART Various types of heat-shrinkable films for packaging dry cell batteries have been seen here and there, with those made of polyvinyl chloride and polyethylene being the most widely used. However, those made of polyvinyl chloride tend to lack the impact weight resistance of the sealed portion and the strength against drop impact, and the packaged products must be handled with care. On the other hand, those made of polyethylene have satisfactory sill strength, but because of their low melting point, they tend to melt during the heat shrinking process and cause holes, and in this respect they cannot be said to be undesirable.
〈発明が解決しようとする課題〉
こうした現状に鑑みシール部の強度に優れると共に熱収
縮工程を行い易い材質の追究をした結果、単品の材質で
はどうしてもこれら全てを満足するものは得にくいこと
が解った。そこで本発明者らは積層熱収縮性フィルムを
検討することにより従来の懸案点の解決を図るべく更に
検討を縁り返した結果遂に本発明に到達した。<Problems to be solved by the invention> In view of the current situation, we have searched for a material that has excellent strength for the sealing part and is easy to perform the heat shrinking process, and as a result, we have found that it is difficult to obtain a material that satisfies all of these requirements with a single material. Ta. Therefore, the present inventors conducted further studies in order to solve the conventional problems by studying laminated heat-shrinkable films, and as a result, they finally arrived at the present invention.
く課題を解決するための手段〉
本発明は、乾電池包装用熱収縮性フィルムにおいてポリ
アミド系樹脂層、接着性樹脂層及びポリエチレン系樹脂
層がこの順序で積層されてなる少なくとも三層を有する
多層フィルムで構成されると共にトータルの厚さを10
〜40μmとした点に特徴を有するものである。Means for Solving the Problems> The present invention provides a heat-shrinkable film for packaging dry batteries, which has at least three layers including a polyamide resin layer, an adhesive resin layer, and a polyethylene resin layer laminated in this order. The total thickness is 10.
It is characterized by having a thickness of ~40 μm.
次に課題を解決するための手段を縛々述べることにする
。Next, I will discuss in detail the means to solve the problem.
本発明に係るポリアミド系樹脂(A)とはナイロン6、
ナイロン66、ナイロン610、ナイロン12などの他
にナイロン6−66共重合体、ナイロン6−610共重
合体などのコポリアミドを例示することができ、更に主
鎖もしくは9111mに芳香族環を有する構造のいわゆ
る芳香族系ポリアミド樹脂も例示できる。また、以上に
例示した各樹脂の混合物等も使用できポリアミド系樹脂
としては特に制限はない。The polyamide resin (A) according to the present invention is nylon 6,
In addition to nylon 66, nylon 610, nylon 12, etc., copolyamides such as nylon 6-66 copolymer and nylon 6-610 copolymer can be exemplified, and furthermore, structures having an aromatic ring in the main chain or 9111m Examples include so-called aromatic polyamide resins. Furthermore, mixtures of the resins exemplified above can also be used, and the polyamide resin is not particularly limited.
接着性樹脂(B)とは変性ポリオレフィン系樹脂、アイ
オノマー樹脂等ポリアミド系樹脂層とポリエチレン系樹
脂層の両者と接着性を有するものならば特に制限はない
、好ましくは前記両者と共に共押出の可能な接着性樹脂
が一層好ましい。The adhesive resin (B) is not particularly limited as long as it has adhesive properties with both the polyamide resin layer and the polyethylene resin layer, such as modified polyolefin resin, ionomer resin, etc., and is preferably one that can be coextruded with both of the above. Adhesive resins are more preferred.
ここで前記した変性ポリオレフィン系樹脂としては、オ
レフィン類の単独又は共重合体等に例えばマレイン酸、
フマル酸、アクリル酸等の不飽和カルボン酸又はその酸
無水物、エステルもしくは金属塩等の誘導体を共重合、
例えばグラフト共重合した変性重合体を代表的なものと
して例示でき、上記変性重合体の単独又は他の成分、例
えば他のポリオレフィン系樹脂との混合物等も前記変性
ポリオレフィン系樹脂の中に含まれる。この際前記した
オレフィン類とは高、中、低密度ポリエチレン、線状低
密度ポリエチレン、エチレン−プロピレン共重合体、エ
チレン−ブテン共重合体、エチレンー二チルーアクリレ
ート共重合体、エチレン−酢酸ビニル共重合体等を例示
できる。The modified polyolefin resins mentioned above include olefins alone or copolymers, such as maleic acid,
Copolymerization of unsaturated carboxylic acids such as fumaric acid and acrylic acid, or derivatives such as their acid anhydrides, esters, and metal salts,
For example, a graft copolymerized modified polymer can be exemplified as a representative example, and the modified polyolefin resins include the modified polyolefin resins alone or in mixtures with other components, such as other polyolefin resins. In this case, the above-mentioned olefins include high, medium, and low density polyethylene, linear low density polyethylene, ethylene-propylene copolymer, ethylene-butene copolymer, ethylene-dithyl acrylate copolymer, and ethylene-vinyl acetate copolymer. Examples include merging.
また、ポリエチレン系樹脂(]としては上記したポリオ
レフィン類と同じものを例示でき、要するにエチレンと
他のオレフィンもしくは非オレフインモノマーとの共重
合体等少なくともエチレン部分を有する共重合体ならば
特に制限は無く、これらの混合物でもよい、また、接着
性樹脂°層に用いる変性エチレン系樹脂、アイオノマー
樹脂(接着性樹脂層と同じものの使用は省く)等も使用
可能である。Examples of the polyethylene resin () include the same as the polyolefins mentioned above, and in short, there is no particular restriction as long as it is a copolymer containing at least an ethylene portion, such as a copolymer of ethylene and another olefin or non-olefin monomer. It is also possible to use a modified ethylene resin, an ionomer resin (the same resin as the adhesive resin layer is not used), etc. used for the adhesive resin layer.
こうした(A)CB)(C)の各樹脂からなる層中には
必要ならば更に他の適宜の第三材料が添加されているこ
とはいつこうに差しつかえない。If necessary, other appropriate third materials may be added to the layer made of each of the resins (A), CB, and (C) at any time.
こうした多層フィルムは前記したfA)(B)(C)層
を基本構成としかつ総厚みがlO〜40μのものならば
全て使用可能であり、好ましい多層フィルムの構成とし
ては
A/B/C,C/B/A/B/C1
B、/B、/A/B/C。Any such multilayer film can be used as long as it has the above-mentioned fA), (B), and (C) layers as its basic structure and has a total thickness of 10 to 40 μm, and the preferred multilayer film structure is A/B/C, C. /B/A/B/C1 B, /B, /A/B/C.
B、/B/A/B/C,B/A/B/C(ここでB、B
、はBと別種の接着性樹脂を示す、)を例示できる。勿
論この他に他の第三成分による樹脂層を施けることも自
由であるが総厚みについでは10〜40μmの範囲が必
要である。B, /B/A/B/C, B/A/B/C (here B, B
, indicates a different type of adhesive resin from B). Of course, it is also possible to apply a resin layer made of another third component, but the total thickness must be in the range of 10 to 40 μm.
ここで総厚みがlOμ以下では強度が不足したり、シー
ル部強度が不十分となる恐れがあり、40μを超えると
厚過ぎて、手ざわりも悪くなり好ましい包装物を提供で
きない。If the total thickness is less than 10μ, the strength may be insufficient or the strength of the seal portion may be insufficient; if it exceeds 40μ, it is too thick and has a poor texture, making it impossible to provide a preferable package.
多層フィルムを構成する個々の層の好ましい厚さを述べ
ることにする。ポリアミド層は5〜15μ、接着性樹脂
層は1−10μ、エチレン系重合体層は1〜15μ程度
を例示できるが特に制限はなく、適宜な値を選択し、ト
ータルの厚さを本発明の範囲とすればよい。The preferred thicknesses of the individual layers constituting the multilayer film will now be stated. For example, the polyamide layer may have a thickness of 5 to 15μ, the adhesive resin layer may have a thickness of 1 to 10μ, and the ethylene polymer layer may have a thickness of approximately 1 to 15μ. It may be a range.
乾電池を包装するには、乾電池複数個を一括して包装し
ても1個ずつ包装してもよいが、一般には2個もしくは
4個を一括して集積包装することが行なわれる。To package dry batteries, a plurality of dry batteries may be packaged together or one by one, but generally two or four batteries are packaged together.
包装形態としてはオーバーラツプ包装、スリブ包装等何
でもよいが、一般には複数個の乾電池を該電池の軸方向
が包装形態の軸方向と直角になるようにオーバーラツプ
し、所定部を溶断シールもしくは背貼り状に圧着シール
してその内角方向をカットし、熱収縮を行うことにより
一括包装するいわゆるスリーブ状包装が多く行われ、こ
の際複数値の乾電池がバラバラにならないように包装さ
れていれば十分で、乾電池全体を包んでいなくてもよい
ことは勿論である。The packaging may be of any type, such as overlap packaging or sleeve packaging, but generally multiple dry batteries are overlapped so that the axial direction of the batteries is perpendicular to the axial direction of the packaging, and predetermined portions are fused and sealed or pasted on the back. Sleeve-shaped packaging is often used, in which the batteries are crimped and sealed, the inner corners are cut, and the batteries are heat-shrinked. Of course, it is not necessary to wrap the entire dry battery.
本発明は共押出等適宜の装置を用いインフレート法によ
りチューブ状フィルム、もしくは共押出Tダイ法により
フラット状フィルム等として成膜すればよいが、特に制
限はない、しかしながら熱収縮性を有する必要があり、
熱収縮性については特に制限はないが、例えば100℃
での熱水に30秒浸漬した際に走行方向に5%以上、走
行方向と直角方向に20%以上、好ましくは前者5〜3
0%、後者30〜60%程度の熱収縮率のものを好適な
ものとして例示できる。In the present invention, the film may be formed as a tube-shaped film by the inflation method using an appropriate device such as co-extrusion, or a flat-shaped film by the co-extrusion T-die method, but there is no particular restriction, however, it is necessary to have heat shrinkability. There is,
There are no particular restrictions on heat shrinkage, but for example, 100°C
When immersed in hot water for 30 seconds at
Examples of preferable examples include those having a heat shrinkage rate of 0%, and the latter having a heat shrinkage rate of about 30 to 60%.
熱収縮性を付与せしめるためには延伸を行う必要があり
、延伸については成膜−冷却後再過熱して行う方法を例
示でき、成膜と延伸を連続で行うも、別工程で行うもど
ちらでもよい、更に溶融延伸法、即ち押出し製膜と延伸
とを同時に行う方法により熱収縮性を付与してもよい、
延伸倍率も特に制限はないが、例えば縦に1.0〜4倍
、横に2〜5倍程度を例示でき、延伸温度も特に制限は
ないが、通常は60〜150℃、好ましくは70〜12
0℃程度を例示できる。In order to impart heat shrinkability, it is necessary to perform stretching, and an example of stretching is a method in which film formation is performed by cooling and then reheating. Furthermore, heat shrinkability may be imparted by a melt-stretching method, that is, a method in which extrusion film formation and stretching are performed simultaneously.
The stretching ratio is also not particularly limited, but can be, for example, 1.0 to 4 times in the vertical direction and 2 to 5 times in the horizontal direction, and the stretching temperature is also not particularly limited, but is usually 60 to 150°C, preferably 70 to 70°C. 12
An example is about 0°C.
以上は本発明の好ましい構成を例示的に説明したまでで
、本発明がかかる記載に制限を受けることなく、その請
求の範囲に沿ってあらゆる態様を取ることが可能である
。The preferred configurations of the present invention have been described above by way of example, and the present invention is not limited to such descriptions and can take on any embodiments within the scope of the claims.
実施例 l
ナイロン6−66共重合体(A)、!水マレイン酸がク
ラフト共重合された変性直鎖状低密度ポリエチレンを含
む接着性樹脂(B)、直鎖状低密度ポリエチレン(C)
をC,/B/A/B/C(7)5層構成としてフラット
状に共押出し、しかる後温度80℃で3倍に縦方向にロ
ール延伸し続いて温度100℃で4倍にテンターにより
横方向に延伸し、100℃の30秒熱水での熱収縮率が
縦方向に20%、横方向に40%の熱収縮性フィルムを
得た。かかるフィルムの全厚は18μm、A層は10μ
m、B層は両方共2μm、C層は両方共2μmであった
。C層はヒートシール層としての作用をするものであっ
た。Example l Nylon 6-66 copolymer (A),! Adhesive resin containing modified linear low-density polyethylene (B), linear low-density polyethylene (C) containing water-maleic acid kraft copolymerized
C, /B/A/B/C (7) were co-extruded into a 5-layer structure in a flat shape, then longitudinally stretched 3 times at a temperature of 80°C, and then stretched 4 times by a tenter at a temperature of 100°C. A heat-shrinkable film was obtained by stretching in the transverse direction and having a heat shrinkage rate of 20% in the longitudinal direction and 40% in the transverse direction in hot water at 100° C. for 30 seconds. The total thickness of such a film is 18 μm, and the A layer is 10 μm.
Both the m and B layers were 2 μm in thickness, and the C layers were both 2 μm in thickness. The C layer acted as a heat seal layer.
こうして得たフィルムを所定寸法にカットし、溶断シー
ルによりスリーブ状とした。かかるスリーブに単■乾電
池4個をその軸方向がスリーブの軸方向と直角となるよ
うに挿入し、熱収縮じしめたところ、4個がしっかりと
係合され、見た目の美しい包装物ができ上がった。The film thus obtained was cut into a predetermined size and made into a sleeve by fusing and sealing. When four D batteries were inserted into the sleeve so that their axial direction was perpendicular to the axial direction of the sleeve and heat-shrinked, the four batteries were firmly engaged and a beautiful-looking package was completed. .
比較例
ポリ塩化ビニルを常法により延伸せしめ、厚さ25μm
、熱収縮率が30秒熱水で縦方向に20%、横方向に4
0%の熱収縮性フィルムを作成した。Comparative Example Polyvinyl chloride was stretched by a conventional method to a thickness of 25 μm.
, the heat shrinkage rate is 20% in the longitudinal direction and 4 in the transverse direction in hot water for 30 seconds.
A 0% heat shrinkable film was created.
こうして得たフィルムと首記実施例で得たフィルムの耐
衝撃強度及び落下衝撃強度の比較を第1表に示した。Table 1 shows a comparison of the impact strength and drop impact strength of the film thus obtained and the film obtained in the above examples.
第 1 表
〈発明の効果〉
本発明は乾電池包装用に好適な熱収縮性フィルムがあり
、かかるフィルムを用いて乾電池を包装した場合熱収縮
作業が容易な上に、シール部での強度が優れ、輸送時、
取扱い時等に包装が破れるという事故が極めて少なく、
美しい包装が確保される等の格別なる効果を奏する。Table 1 <Effects of the Invention> The present invention provides a heat-shrinkable film suitable for packaging dry batteries, and when such a film is used to package dry batteries, the heat-shrinking work is easy and the strength of the sealed portion is excellent. , during transportation,
There are very few accidents where the packaging breaks during handling, etc.
This has special effects such as ensuring beautiful packaging.
Claims (1)
樹脂層が、この順序で積層されてなる少なくとも三層を
有する多層フィルムで構成されると共に、前記多層フィ
ルムのトータルの厚さが10〜40μmであることを特
徴とする乾電池包装用熱収縮性フィルム。It is composed of a multilayer film having at least three layers in which a polyamide resin layer, an adhesive resin layer, and a polyethylene resin layer are laminated in this order, and the total thickness of the multilayer film is 10 to 40 μm. A heat-shrinkable film for packaging dry batteries, which is characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15833390A JPH0449035A (en) | 1990-06-16 | 1990-06-16 | Heat-shrinkable film for packaging dry cell |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15833390A JPH0449035A (en) | 1990-06-16 | 1990-06-16 | Heat-shrinkable film for packaging dry cell |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0449035A true JPH0449035A (en) | 1992-02-18 |
Family
ID=15669353
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15833390A Pending JPH0449035A (en) | 1990-06-16 | 1990-06-16 | Heat-shrinkable film for packaging dry cell |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0449035A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100395557B1 (en) * | 2000-09-21 | 2003-08-25 | 박중헌 | Manufacturing method of non-toxic laminated unoriented nylon film |
| KR100714040B1 (en) * | 2002-12-20 | 2007-05-04 | 에스케이 주식회사 | Molded article with multilayer structure |
-
1990
- 1990-06-16 JP JP15833390A patent/JPH0449035A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100395557B1 (en) * | 2000-09-21 | 2003-08-25 | 박중헌 | Manufacturing method of non-toxic laminated unoriented nylon film |
| KR100714040B1 (en) * | 2002-12-20 | 2007-05-04 | 에스케이 주식회사 | Molded article with multilayer structure |
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