JPH04307239A - Composite polyester type film - Google Patents
Composite polyester type filmInfo
- Publication number
- JPH04307239A JPH04307239A JP15628791A JP15628791A JPH04307239A JP H04307239 A JPH04307239 A JP H04307239A JP 15628791 A JP15628791 A JP 15628791A JP 15628791 A JP15628791 A JP 15628791A JP H04307239 A JPH04307239 A JP H04307239A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- film
- resin layer
- polyester type
- polyester
- 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
- 239000002131 composite material Substances 0.000 title claims abstract description 39
- 229920000728 polyester Polymers 0.000 title abstract description 14
- 229920001225 polyester resin Polymers 0.000 claims abstract description 32
- 239000004645 polyester resin Substances 0.000 claims abstract description 32
- 229920005672 polyolefin resin Polymers 0.000 claims abstract description 20
- 239000004840 adhesive resin Substances 0.000 claims abstract description 19
- 229920006223 adhesive resin Polymers 0.000 claims abstract description 19
- 229920006267 polyester film Polymers 0.000 claims description 41
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 31
- 229920005989 resin Polymers 0.000 abstract description 26
- 239000011347 resin Substances 0.000 abstract description 26
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract description 16
- 229920001577 copolymer Polymers 0.000 abstract description 16
- -1 polyethylene Polymers 0.000 abstract description 9
- 150000002009 diols Chemical class 0.000 abstract description 8
- 238000010030 laminating Methods 0.000 abstract description 8
- 239000002253 acid Substances 0.000 abstract description 6
- 229920001519 homopolymer Polymers 0.000 abstract description 6
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 abstract description 4
- 239000004698 Polyethylene Substances 0.000 abstract description 2
- 229920000554 ionomer Polymers 0.000 abstract description 2
- 229920000573 polyethylene Polymers 0.000 abstract description 2
- 229920001038 ethylene copolymer Polymers 0.000 abstract 1
- 238000003475 lamination Methods 0.000 description 15
- 238000000034 method Methods 0.000 description 14
- 238000007789 sealing Methods 0.000 description 11
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 10
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 5
- 229920000092 linear low density polyethylene Polymers 0.000 description 5
- 239000004707 linear low-density polyethylene Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 238000009820 dry lamination Methods 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 238000000576 coating method Methods 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 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
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 229920006228 ethylene acrylate copolymer Polymers 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000009998 heat setting Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920001179 medium density polyethylene Polymers 0.000 description 2
- 239000004701 medium-density polyethylene Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- 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
- 229920001634 Copolyester Polymers 0.000 description 1
- 229920012753 Ethylene Ionomers Polymers 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920005677 ethylene-propylene-butene terpolymer Polymers 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000002184 metal Chemical class 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000012785 packaging film Substances 0.000 description 1
- 229920006280 packaging film Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、ラミネート強度、ヒー
トシール強度及び透明性が優れた易ヒートシール性複合
ポリエステル系フイルムに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an easily heat-sealable composite polyester film that has excellent lamination strength, heat-seal strength and transparency.
【0002】0002
【従来の技術】従来から、主たる繰返し単位がエチレン
テレフタレートであるホモポリエステル系樹脂からなる
フィルムは強度、剛性、透明性、耐熱性、光沢性、耐薬
品性、衛生上の安全性等に優れており多くの用途に使用
されているがヒートシール性が劣るため単体で包装用フ
ィルムとして使用されることはあまりなかった。[Prior Art] Films made of homopolyester resins whose main repeating unit is ethylene terephthalate have been known to have excellent strength, rigidity, transparency, heat resistance, gloss, chemical resistance, sanitary safety, etc. Although it is used for many purposes, it has rarely been used alone as a packaging film because of its poor heat sealability.
【0003】ホモポリエステル系フィルムにヒートシー
ル性を付与せしめるためには、易ヒートシール性を有す
るプラスチック樹脂を有機溶剤等に溶解した接着剤をコ
ートするコーティング法、或はポリオレフィン系樹脂を
ラミネートもしくは積層してヒートシール性を付与する
方法等がある。[0003] In order to impart heat-sealability to a homopolyester film, a coating method is employed in which a plastic resin having easy heat-sealability is coated with an adhesive prepared by dissolving it in an organic solvent, or a polyolefin resin is laminated or laminated. There are methods of imparting heat-sealing properties.
【0004】ポリオレフィン系樹脂をラミネートもしく
は積層するには種々の方法があるがー般的には、ドライ
ラミネートやホモポリエステル系樹脂に接着性樹脂を介
してポリオレフィン系樹脂を共押出して複合する方法が
採用されていた。[0004] There are various methods for laminating or laminating polyolefin resins, but generally, dry lamination or a method of coextruding a polyolefin resin onto a homopolyester resin via an adhesive resin to form a composite is used. He had been hired.
【0005】[0005]
【発明が解決しようとする問題点】しかしながら、コー
ティングにおいては残留溶剤が問題となり、そのため高
度な乾燥設備や溶剤回収設備等高価な設備投資が必要で
あり、そのため加工費が高くなる欠点があった。[Problem to be solved by the invention] However, residual solvent is a problem in coating, which requires expensive equipment investment such as advanced drying equipment and solvent recovery equipment, which has the disadvantage of increasing processing costs. .
【0006】接着剤によるシールの場合はフイルムを折
畳んでシールするとフイルムの弾性に基ずく反発作用に
よりシール部が離れやすい問題がある。[0006] In the case of adhesive sealing, there is a problem in that when the film is folded and sealed, the sealed portion tends to separate due to the repulsive action based on the elasticity of the film.
【0007】ドライラミネート等により易ヒートシール
性フイルムをラミネートするものは工数が多くなり経済
的に不利であるうえに操作も煩雑であり溶剤等による環
境汚染の問題もある。[0007] Laminating easily heat-sealable films by dry lamination or the like requires a large number of man-hours, is economically disadvantageous, and is also complicated to operate, and there is also the problem of environmental pollution due to solvents and the like.
【0008】共押出法により易ヒートシール性樹脂層を
積層したものはヒートシール性があり用途によっては使
用できるが、更に強いラミネート強度及びヒートシール
強度が要求される用途、例えば重量物の包装袋、重量物
を包装した包装物品の輸送等をする場合には不適当であ
りラミネート強度及びヒートシール強度の向上が要求さ
れている。A product in which easily heat-sealable resin layers are laminated by a coextrusion method has heat-sealability and can be used in some applications, but it can be used in applications that require even stronger lamination strength and heat-sealing strength, such as packaging bags for heavy items. However, it is not suitable for transporting packaged articles containing heavy items, and improvements in lamination strength and heat sealing strength are required.
【0009】[0009]
【発明が解決するための手段】本発明は基材層であるポ
リエステル系フイルムの少なくとも片面に変性ポリエス
テル系樹脂を積層してなる少なくとも2層構成を有する
複合フイルムと、2層構成を有する複合ポリエステル系
フイルムの変性ポリエステル糸樹脂層側に接着性樹脂を
介してポリオレフィン系樹脂を積層した少なくとも4層
構成からなる複合ポリエステル系フイルムに関する。Means for Solving the Invention The present invention provides a composite film having at least a two-layer structure obtained by laminating a modified polyester resin on at least one side of a polyester film serving as a base layer, and a composite polyester film having a two-layer structure. The present invention relates to a composite polyester film having at least a four-layer structure in which a polyolefin resin is laminated on the modified polyester thread resin layer side of the film via an adhesive resin.
【0010】本発明における基材層となるポリエステル
系フイルムとは主たる繰返単位がエチレンテレフタレー
トのホモポリマーからなるものを対象とするが必ずしも
これのみに限定されず、ポリエチレンテレフタレートに
おける酸成分が90モル%以上のテレフタル酸と10モ
ル%未満のテレフタル酸以外のジカルボン酸、例えばイ
ソフタル酸、ナフタリンジカルボン酸等の芳香族ジカル
ボン酸、ヘキサヒドロテレフタル酸、ヘキサイソフタル
酸等の脂環族ジカルボン酸、アジピン酸、セバチン酸等
の脂肪族ジカルボン酸等及びこれ等の誘導体の1種以上
とから構成され、ジオール成分がエチレングリコール及
び/又はエチレングリコール以外のジオール成分、例え
ばジエチレングリコール、トリメチレングリコール、テ
トラメチレングリコール、1・4シクロヘキサンジメタ
ノール等及びこれ等の誘導体の1種以上で構成されて成
るコポリマーからなるもの、或はポリエチレンテレフタ
レートホモポリマーと前記コポリマーの混合物からなる
もの等が例示できる。[0010] The polyester film serving as the base material layer in the present invention is intended to be one in which the main repeating unit is a homopolymer of ethylene terephthalate, but is not necessarily limited to this. % or more of terephthalic acid and less than 10 mol% of dicarboxylic acids other than terephthalic acid, such as aromatic dicarboxylic acids such as isophthalic acid and naphthalene dicarboxylic acid, alicyclic dicarboxylic acids such as hexahydroterephthalic acid and hexaisophthalic acid, and adipic acid. , aliphatic dicarboxylic acids such as sebacic acid, and one or more derivatives thereof, and the diol component is ethylene glycol and/or a diol component other than ethylene glycol, such as diethylene glycol, trimethylene glycol, tetramethylene glycol, Examples include a copolymer composed of 1,4 cyclohexanedimethanol and one or more derivatives thereof, and a mixture of a polyethylene terephthalate homopolymer and the copolymer.
【0011】本発明に係る変性ポリエステル系樹脂とは
、特に制限されないが、酸成分が50〜90モル%のテ
レフタル酸と10〜50モル%の、例えばイソフタル酸
、アジピン酸、セバチン酸等及びこれ等の誘導体の1種
以上とから構成され、ジオール成分がエチレングリコー
ル及び/又はエチレングリコール以外のジオール成分、
例えばジエチレングリコール、ネオペンチルグリコール
、1・4シクロヘキサンジメタノール、1・4ブタンジ
オール等及びこれ等の誘導体の1種以上で構成されて成
るコポリマー、或はこれ等コポリマーと前記したポリエ
チレンテレフタレートホモポリマーとの混合物を例示で
きる。The modified polyester resin according to the present invention is not particularly limited, but has an acid component of 50 to 90 mol% of terephthalic acid and 10 to 50 mol% of isophthalic acid, adipic acid, sebacic acid, etc. The diol component is ethylene glycol and/or a diol component other than ethylene glycol,
For example, a copolymer composed of one or more of diethylene glycol, neopentyl glycol, 1,4 cyclohexanedimethanol, 1,4 butanediol, etc. and their derivatives, or a copolymer of these and the above-mentioned polyethylene terephthalate homopolymer. A mixture can be exemplified.
【0012】変性ポリエステル系樹脂のテレフタル酸成
分が90モル%以上になるとヒートシール性が低下する
場合があり、50モル%以下になると機械的強度が低下
し成膜性も著しく低下する傾向があり、又ブロッキング
等も発生する場合が多いが、用途によっては使用可能で
ある。[0012] When the terephthalic acid component of the modified polyester resin exceeds 90 mol%, the heat sealing properties may deteriorate, and when the content falls below 50 mol%, the mechanical strength tends to decrease and the film forming properties tend to decrease significantly. , blocking, etc. often occur, but it can be used depending on the application.
【0013】本発明に係る4層構成の複合ポリエステル
系フィルムに用いる接着性樹脂としてはエチレン−プロ
ピレン共重合体、プロピレン共重合体、プロピレン−ブ
テン共重合体、変性ポリオレフィン系樹脂、アイオノマ
ー等を例示できるが、変性ポリエステル系樹脂層とポリ
オレフィン系樹脂層とを接着できるものであればこれ以
外でもよく、特に制限されない。Examples of the adhesive resin used in the four-layer composite polyester film according to the present invention include ethylene-propylene copolymer, propylene copolymer, propylene-butene copolymer, modified polyolefin resin, and ionomer. However, any other material may be used as long as it can bond the modified polyester resin layer and the polyolefin resin layer, and is not particularly limited.
【0014】変性ポリオレフィン系樹脂としては、オレ
フィン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酸無水物、
エステルもしくは金属塩の誘導体を共重合、例えばグラ
フト重合した変性共重合体を代表的なものとして例示で
きる。上記変性共重合体の単独又はその他の成分、例え
ばポリオレフィン系樹脂との混合物も変性ポリオレフィ
ン系樹脂に含まれる。この際、ポリオレフィン系樹脂と
は、低、中、高密度ポリエチレン、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−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。Modified polyolefin resins include olefin homopolymers or copolymers, unsaturated carboxylic acids or acid anhydrides such as maleic acid, fumaric acid, acrylic acid, etc.
Typical examples include modified copolymers obtained by copolymerizing, for example graft polymerizing, ester or metal salt derivatives. The modified polyolefin resins include the modified copolymers described above alone or in mixtures with other components, such as polyolefin resins. In this case, polyolefin resins include low, medium, and high density polyethylene, linear low density polyethylene, ethylene-propylene copolymer, ethylene-butene copolymer, ethylene-acrylate copolymer, and ethylene-vinyl acetate copolymer. Examples include merging.
【0015】変性ポリエステル系樹脂層に接着性樹脂を
介して積層されるポリオレフィン系樹脂としては、特に
制限はないが、低、中、高密度ポリエチレン、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−プロピレン−ブテン
3元共重合体、エチレン−アクリレート共重合体、エチ
レン−酢酸ビニル共重合体、アイオノマー等を例示でき
る。この場合、これ等の混合物もポリオレフィン系樹脂
に含まれる。The polyolefin resin laminated on the modified polyester resin layer via an adhesive resin is not particularly limited, but includes low, medium, and high density polyethylene, linear low density polyethylene, and ethylene-propylene copolymer. , ethylene-butene copolymer, ethylene-propylene-butene terpolymer, ethylene-acrylate copolymer, ethylene-vinyl acetate copolymer, and ionomer. In this case, a mixture of these is also included in the polyolefin resin.
【0016】本発明の複合ポリエステル系フイルムを積
層するには、特に制限はないが、共押出法、ドライラミ
ネート法、押出ラミネート法、熱圧着ラミネート法等を
例示できるが共押出法が便利である。The method for laminating the composite polyester film of the present invention is not particularly limited, but examples include coextrusion, dry lamination, extrusion lamination, thermocompression lamination, etc., with coextrusion being convenient. .
【0017】共押出法とは、2層構成のフイルムを成膜
する場合には、少なくとも2台の押出機をフラット状多
層ダイス、或は環状多層ダイスと結合し、1台の押出機
にポリエステル系樹脂を、もう1台の押出機には変性ポ
リエステル系樹脂を供給して加熱された前記多層ダイス
に導入し多層ダイス内もしくは多層ダイス外で接合して
押出す方法を例示できる。[0017] In the coextrusion method, when forming a two-layer film, at least two extruders are combined with a flat multilayer die or an annular multilayer die, and one extruder extrudes polyester. An example of a method is to supply a modified polyester resin to another extruder, introduce the resin into the heated multilayer die, join within or outside the multilayer die, and extrude.
【0018】4層構成を有する複合ポリエステル系フイ
ルムを成膜する場合には、少なくとも4台の押出機を用
いて、1台はポリエステル系樹脂、他の1台には変性ポ
リエステル系樹脂、更に他の1台には接着性樹脂、更に
もう1台にはポリオレフィン系樹脂を供給し、加熱され
た共押出多層ダイスに導入し多層ダイス内もしくは多層
ダイス外で溶融状態で接合して共押出する方法を例示で
きる。更に必要ならば少なくとも1台以上の押出機を結
合し複合ポリエステル系フイルムの表面、中間などに積
層しても本発明に包含される。[0018] When forming a composite polyester film having a four-layer structure, at least four extruders are used, one extruder extruding polyester resin, the other one extruding modified polyester resin, and the other extruder extruder extruder extruder. A method of supplying adhesive resin to one machine and polyolefin resin to the other machine, introducing them into a heated coextrusion multilayer die, joining them in a molten state inside or outside the multilayer die, and coextruding them. can be exemplified. Furthermore, if necessary, at least one extruder may be connected to the composite polyester film to laminate it on the surface or in the middle thereof, which is also included in the present invention.
【0019】本発明の複合ポリエステル系フイルムを延
伸するには特に制限はなく、例えば加熱ロールで縦方向
に延伸後テンターに送り込みフイルムの両端を保持しな
がら横方向に延伸し、次いでテンター後室で熱処理を施
し熱固定をする逐次2軸延伸法を例示できるが、これの
みに限定されず同時2軸延伸、1軸延伸、或はこれ等を
組み合わせて延伸してもよく、又は環状多層ダイスでチ
ューブ状複合フイルムを成膜してチューブ状同時2軸延
伸をしてもよく特に制限はない。There are no particular restrictions on how to stretch the composite polyester film of the present invention. For example, after being stretched in the longitudinal direction with heated rolls, the film is fed into a tenter and stretched in the transverse direction while holding both ends of the film, and then in the rear chamber of the tenter. An example is a sequential biaxial stretching method in which heat treatment is performed and heat setting is performed, but the method is not limited to this, and simultaneous biaxial stretching, uniaxial stretching, or a combination of these may be used, or stretching may be performed using a circular multilayer die. A tubular composite film may be formed and simultaneously biaxially stretched into a tubular shape without any particular limitation.
【0020】延伸条件としては、特に制限はないが縦方
向の延伸温度は60〜100℃、延伸倍率は2〜6倍、
横方向の延伸温度は60〜130℃、延伸倍率は2〜1
0倍、熱固定温度は150〜250℃、3〜10秒を例
示できる。The stretching conditions are not particularly limited, but the stretching temperature in the longitudinal direction is 60 to 100°C, the stretching ratio is 2 to 6 times,
The stretching temperature in the transverse direction is 60 to 130°C, and the stretching ratio is 2 to 1.
For example, the heat setting temperature is 150 to 250°C for 3 to 10 seconds.
【0021】本発明の複合ポリエステル系フイルムにお
いて、ホモポリエステルフイルムとコポリエステルフイ
ルムの2層構成の複合フイルムの場合、ホモポリエステ
ル系樹脂と変成ポリエステル系樹脂は共にポリエステル
系樹脂の範ちゅうであるので相溶性がよく、溶融してい
る相間は互いに混じり合いあたかもポリエステル系樹脂
だけが溶融しているかのようになりポリエステル系樹脂
1層と見なすことができる場合が多く、したがって相間
でのラミネート強度は強くなり剥離は発生しにくくなる
傾向に成りがちである。In the composite polyester film of the present invention, in the case of a composite film having a two-layer structure of a homopolyester film and a copolyester film, the homopolyester resin and the modified polyester resin are both in the category of polyester resins, so they are compatible with each other. It has good solubility, and the molten phases mix with each other, making it appear as if only the polyester resin is molten, and can often be considered as one layer of polyester resin, thus increasing the lamination strength between the phases. Peeling tends to be less likely to occur.
【0022】ホモポリエステル系樹脂と変性ポリエステ
ル系樹脂の透明性は略略同等と見なされ良好であるので
溶融積層された本発明に係る複合ポリエステル系フイル
ムの透明性も優れたものとなる場合が多い。Since the transparency of the homopolyester resin and the modified polyester resin are considered to be substantially the same and are good, the transparency of the melt-laminated composite polyester film according to the present invention is often excellent.
【0023】更にホモポリエステル系フイルムは結晶化
するとヒートシール性が劣るが変性ポリエステル系フイ
ルムは非晶質成分やガラス転移点(Tg)を下げる成分
が含まれているのでヒートシールを有しており、ホモポ
リエステル系樹脂層と変性ポリエステル系樹脂層を積層
した複合ポリエステル系フイルムにヒートシール性が付
与される。この複合ポリエステル系フイルムは前記の理
由によりラミネート強度が強いためヒートシール強度も
強いものとなる傾向を有することが多い。Furthermore, homopolyester films have poor heat-sealability when crystallized, but modified polyester films contain amorphous components and components that lower the glass transition point (Tg), so they are heat-sealable. Heat sealability is imparted to a composite polyester film in which a homopolyester resin layer and a modified polyester resin layer are laminated. Due to the above-mentioned reasons, this composite polyester film has a strong lamination strength, and thus tends to have a strong heat seal strength as well.
【0024】本発明に係る4層構成の複合ポリエステル
系フイルムにおいても、ポリエステル系樹脂と変性ポリ
エステル系樹脂は共にポリエステル系樹脂であるので相
溶性がよく溶融積層すれば境界面は溶融混合し、あたか
も1層のポリエステル系樹脂層であるかのようになる。
従って4層構成であっても、ポリエステル系樹脂層/接
着性樹脂層/ポリオレフィン系樹脂層の3層構造と見な
すことができ、ポリエステル系樹脂層と変性ポリエステ
ル系樹脂層とのラミネート強度は強いものとなる場合が
多い。In the composite polyester film having a four-layer structure according to the present invention, the polyester resin and the modified polyester resin are both polyester resins, so they have good compatibility, and when melt-laminated, the interface melts and mixes, as if it were It looks like one layer of polyester resin. Therefore, even if it has a four-layer structure, it can be considered as a three-layer structure of polyester resin layer/adhesive resin layer/polyolefin resin layer, and the lamination strength of the polyester resin layer and modified polyester resin layer is strong. In many cases.
【0025】一般的に変性ポリエステル系樹脂層と接着
性樹脂層との接着強度はホモポリエステル系樹脂層と接
着性樹脂層との接着強度よりも強くなる傾向があるので
、本発明の複合ポリエステル系フイルムは、従来のホモ
ポリエステル系樹脂層/接着性樹脂層/ポリオレフィン
系樹脂層構成からなる複合ポリエステル系フイルムより
もラミネート強度、ヒートシール強度が強くなる傾向が
ある。Generally, the adhesive strength between the modified polyester resin layer and the adhesive resin layer tends to be stronger than the adhesive strength between the homopolyester resin layer and the adhesive resin layer. The film tends to have stronger lamination strength and heat seal strength than a conventional composite polyester film having a homopolyester resin layer/adhesive resin layer/polyolefin resin layer structure.
【0026】しかも本発明の複合ポリエステル系フイル
ムはポリエステル系フイルムの優れた物性である機械的
性質、寸法安定性、耐熱性、化学的安定性、透明性、光
沢性、衛生上の安定性等を維持し優れたラミネート強度
、ヒートシール強度が付与されたものである。Moreover, the composite polyester film of the present invention has the excellent physical properties of polyester films such as mechanical properties, dimensional stability, heat resistance, chemical stability, transparency, gloss, and hygienic stability. It maintains excellent lamination strength and heat seal strength.
【0027】本発明の複合ポリエステル系フイルムの厚
みは用途によって適宜に設定すれば良いが、一般的には
、基材層のポリエステル系フイルムが7〜20μ、変性
ポリエステル系共重合体層が2〜15μ、接着性樹脂層
が2〜5μ、ポリオレフィン系樹脂層が10〜70μを
例示でできるが、これのみに制限されず用途によっては
これ以外でもよい。[0027] The thickness of the composite polyester film of the present invention may be set appropriately depending on the application, but generally, the thickness of the polyester film of the base layer is 7 to 20 μm, and the thickness of the modified polyester copolymer layer is 2 to 2 μm. For example, the adhesive resin layer may have a thickness of 15μ, the adhesive resin layer may have a thickness of 2 to 5μ, and the polyolefin resin layer may have a thickness of 10 to 70μ.
【0028】本発明の複合ポリエステル系フイルムは必
要に応じて印刷を行なう場合には、グラビア印刷機等適
宜な方法によって表印刷、裏印刷等をおこなえばよく、
特に好ましい例としては、別のフイルムに印刷を行ない
印刷面が複合ポリエステル系に接するように適宜な方法
でラミネートする方法を例示できるが、このことに特に
制限はない。When the composite polyester film of the present invention is printed as necessary, it may be printed on the front side, the back side, etc. using an appropriate method such as a gravure printing machine.
A particularly preferred example is a method of printing on another film and laminating it by an appropriate method so that the printed surface is in contact with the composite polyester, but there is no particular restriction on this method.
【0029】必要ならば、コロナ放電処理や樹脂等を有
機溶剤等に溶解した溶液をコーティングしたり、ポリエ
ステル系樹脂やポリオレフィン系樹脂と同種もしくは異
種の樹脂やフイルムを押出ラミネート、ドライラミネー
ト等をしてもよく、特にこのことに制限はない。If necessary, corona discharge treatment, coating with a solution of a resin etc. dissolved in an organic solvent, etc., extrusion lamination, dry lamination, etc. of a resin or film of the same or different type as the polyester resin or polyolefin resin may be performed. There is no particular restriction on this.
【0030】本発明の複合ポリエステル系フイルムを構
成する各樹脂に、必要ならば樹脂、アンチブロッキング
剤、滑剤、顔料、界面活性剤、紫外線防止剤、安定剤、
充填剤等を添加してもよく、このことに特に制限はない
。[0030] If necessary, resins, anti-blocking agents, lubricants, pigments, surfactants, ultraviolet inhibitors, stabilizers,
Fillers and the like may be added, and there are no particular restrictions on this.
【0031】本発明の複合ポリエステル系フイルムは特
に制限されないが、各種の食品、機械部品、重量物の包
装、重量物(例えば、水物)包装物を積み重ねて搬送す
る際の袋、或は特に透明性が要求される物品の包装等に
好適である。Although the composite polyester film of the present invention is not particularly limited, it can be used as packaging for various foods, machine parts, heavy items, bags for stacking and transporting packages of heavy items (for example, water items), or in particular, Suitable for packaging products that require transparency.
【0032】[0032]
【実施例】以下実施例について詳述する。
実施例1
バレル内径40mmの押出機にジカルボン酸成分として
テレフタル酸100モル%、ジオール成分としてエチレ
ングリコール100モル%からなるホモポリエステル樹
脂(A)、他のバレル内径40mmの押出機に酸成分と
してテレフタル酸85モル%、イソフタル酸15モル%
とグリコール成分としてエチレングリコール85モル%
、ジエチレングリコール15モル%とからなる変性ポリ
エステル樹脂(B)を供給し250℃に加熱したフラッ
ト状共押出ダイスに送り込みダイス内で(A)と(B)
を積層させ2層の溶融状フラットフイルムを押出した。
該フイルムはホモポリマー層とコポリマー層の境界面は
溶融混合しあたかも1層であるかのようになった。次い
で該フイルムを冷却水が循環する冷却ロール(30℃)
で冷却固化し遅(前)駆動ロールと速(後)駆動ロール
間の85℃に加熱されたロールで縦方向に3倍延伸後テ
ンターに入りフイルム両端を保持して100℃に加熱し
横方向に4倍延伸し、その後同テンターの後室で240
℃、5秒熱処理した2軸延伸複合ポリエステルフイルム
をえた。[Example] Examples will be described in detail below. Example 1 A homopolyester resin (A) consisting of 100 mol% of terephthalic acid as a dicarboxylic acid component and 100 mol% of ethylene glycol as a diol component was placed in an extruder with a barrel inner diameter of 40 mm, and terephthal was added as an acid component in another extruder with a barrel inner diameter of 40 mm. Acid 85 mol%, Isophthalic acid 15 mol%
and 85 mol% ethylene glycol as glycol component
, diethylene glycol and 15 mol % of the modified polyester resin (B) was fed into a flat coextrusion die heated to 250°C, and (A) and (B) were mixed in the die.
were laminated to extrude two layers of molten flat film. In this film, the interface between the homopolymer layer and the copolymer layer was melt-mixed and became as if they were one layer. Next, a cooling roll (30°C) where cooling water circulates through the film.
After being cooled and solidified, the film is stretched 3 times in the longitudinal direction with rolls heated to 85°C between a slow (front) drive roll and a fast (rear) drive roll, then entered into a tenter and heated to 100°C while holding both ends of the film, and then stretched in the transverse direction. Stretched to 4 times, then 240
A biaxially stretched composite polyester film was obtained which was heat-treated at ℃ for 5 seconds.
【0033】この複合ポリエステルフイルムはホモポリ
エステル層と変性ポリエステル層が完全に溶融積層し1
層のポリエステルフイルムであるかのようになっている
ので、ラミネート剥離は発生しなかった。ヒートシール
強度はヒートシール温度180℃、シール圧力2Kg/
cm2,シール時間1秒の条件で1.0〜1.2Kg/
15mmであった。透明度は2.1%(Haze)、ホ
モポリエステルフイルム/ポリオレフィン系フイルムの
複合フイルムの透明度4.5%(Haze)より優れて
いた。[0033] This composite polyester film has a homopolyester layer and a modified polyester layer completely melted and laminated.
Lamination delamination did not occur because the layers appeared to be polyester films. Heat sealing strength is heat sealing temperature 180℃, sealing pressure 2kg/
cm2, 1.0-1.2Kg/ under the conditions of sealing time of 1 second
It was 15 mm. The transparency was 2.1% (Haze), which was superior to the transparency of the homopolyester film/polyolefin film composite film, 4.5% (Haze).
【0034】実施例2
バレル内径50mmの押出機にジカルボン酸成分として
テレフタル酸100モル%とジオーリル成分としてエチ
レングリコール100モル%とからなるポリエチレンテ
レフタレート樹脂(A)を、バレル内径40mmの押出
機3台の各々に酸成分としてテレフタル酸70モル%、
イソフタル酸30モル%とグリコール成分としてエチレ
ングリコール100モル%とからなる変性ポリエステル
系樹脂(B)、マレイン酸をグラフト重合した変性ポリ
エチレン樹脂(C)、線状低密度ポリエチレン樹脂(D
)を供給し、250℃に加熱したフラット状共押出多層
ダイス内でA/B/C/Dとなるように積層した溶融フ
ラットフイルムを押出した。次いで冷却水が循環する冷
却ロール(30℃)で冷却固化し、遅(前)駆動ロール
と速(後)駆動ロールと90℃の加熱ロールで縦方向に
3倍延伸後テンターに入りフイルム両端を保持して12
0℃に加熱して横方向に4倍延伸を行ない、その後テン
ター後室でフイルム両端を保持したまま240℃、5秒
熱処理し熱固定した2軸延伸複合ポリエステルフイルム
をえた。Example 2 A polyethylene terephthalate resin (A) consisting of 100 mol% of terephthalic acid as a dicarboxylic acid component and 100 mol% of ethylene glycol as a diol component was placed in three extruders with a barrel inner diameter of 40 mm. 70 mol% of terephthalic acid as an acid component,
A modified polyester resin (B) consisting of 30 mol% of isophthalic acid and 100 mol% of ethylene glycol as a glycol component, a modified polyethylene resin (C) obtained by graft polymerization of maleic acid, and a linear low-density polyethylene resin (D).
) was supplied, and a molten flat film laminated in A/B/C/D was extruded in a flat coextrusion multilayer die heated to 250°C. Next, the film is cooled and solidified using a cooling roll (30°C) where cooling water circulates, and stretched 3 times in the longitudinal direction using a slow (front) drive roll, a fast (rear) drive roll, and a 90°C heating roll, and then enters a tenter and both ends of the film are stretched. hold 12
The film was heated to 0° C. and stretched 4 times in the transverse direction, and then heat-treated at 240° C. for 5 seconds while holding both ends of the film in the rear chamber of a tenter to obtain a heat-set biaxially stretched composite polyester film.
【0035】この複合ポリエステルフイルムの変性ポリ
エステル樹脂層(B)と接着性樹脂層(C)とのラミノ
ート強度は200〜230g/15mmであり、複合ポ
リエステルフイルムの線状低密度ポリエチレン同志のヒ
ートシール強度はヒートシール温度180℃,ヒートシ
ール圧力2Kg/cm2,ヒートシール時間1秒の条件
で1.3〜1.5Kg/15mmであった。The laminated strength of the modified polyester resin layer (B) and the adhesive resin layer (C) of this composite polyester film is 200 to 230 g/15 mm, and the heat seal strength of the linear low density polyethylene of the composite polyester film is 200 to 230 g/15 mm. was 1.3 to 1.5 Kg/15 mm under the conditions of a heat seal temperature of 180 DEG C., a heat seal pressure of 2 Kg/cm2, and a heat seal time of 1 second.
【0036】[0036]
【比較例】実施例で用いたホモポリエステル系樹脂(A
),マレイン酸をグラフト重合したポリエチレン系接着
性樹脂(C),線状低密度ポリエチレン樹脂(D)を実
施例と同様な方法でA/C/Dの複合ポリエステル系フ
イルムをえた。[Comparative example] Homopolyester resin (A
), a polyethylene adhesive resin (C) graft-polymerized with maleic acid, and a linear low-density polyethylene resin (D) were used in the same manner as in Examples to obtain an A/C/D composite polyester film.
【0037】この複合ポリエステル系フイルムのホモポ
リエステル系樹脂層と接着性樹脂層とのラミネート強度
は150〜160g/15mm.線状低密度樹脂同志の
ヒートシール強度は実施例と同じ条件で800〜900
g/15mmであった。The lamination strength of the homopolyester resin layer and adhesive resin layer of this composite polyester film is 150 to 160 g/15 mm. The heat sealing strength of the linear low-density resins was 800 to 900 under the same conditions as in the example.
g/15mm.
【0038】これから明らかなように、本発明の複合ポ
リエステル系フイルムは比較例のホモポリエステル系フ
イルム/接着性樹脂層/ポリオレフィン系樹脂層からな
る複合ポリエステル系フイルムよりもポリエステル系フ
イルムと接着性樹脂層間のラミネート強度、ヒートシー
ル強度が強く軽量物から重量物までの広い範囲の包装が
可能となった。As is clear from this, the composite polyester film of the present invention has a stronger bond between the polyester film and the adhesive resin layer than the composite polyester film of the comparative example consisting of a homopolyester film/adhesive resin layer/polyolefin resin layer. Its lamination strength and heat seal strength are strong, making it possible to package a wide range of items from light to heavy items.
【0039】[0039]
【発明の効果】本発明は以上の通りであり、ヒートシー
ル性が劣る主たる繰り返し単位がエチレンテレフタレー
トからなるポリエステル系フイルムにポリエステル系フ
イルムの有する特性を阻害せずヒートシール性を付与さ
せた複合ポリエステル系フイルムを提供するものである
。Effects of the Invention The present invention is as described above, and is a composite polyester in which heat sealability is imparted to a polyester film whose main repeating unit is ethylene terephthalate, which has poor heat sealability, without inhibiting the properties of the polyester film. It provides films based on the following.
【0040】本発明の複合ポリエステル系フイルムは、
特にラミネート強度、ヒートシール強度が優れ軽量物か
ら重量物までの包装が可能なもので、今後広い用途が期
待できる。[0040] The composite polyester film of the present invention is
In particular, it has excellent lamination strength and heat sealing strength, and can be used to package lightweight to heavy items, and is expected to have a wide range of applications in the future.
Claims (2)
なくとも片面に変性ポリエステル系樹脂層を積層した少
なくとも2層構成を有する複合ポリエステル系フイルム
。1. A composite polyester film having at least a two-layer structure in which a modified polyester resin layer is laminated on at least one side of a polyester film as a base layer.
ル系樹脂層から成る積層フイルムの変性ポリエステル系
樹脂層側に接着性樹脂層を介してポリオレフィン系樹脂
層を積層した少なくとも4層構成からなる複合ポリエス
テル系フイルム。Claim 2: A composite polyester film consisting of at least four layers, in which a polyolefin resin layer is laminated on the modified polyester resin layer side of a laminated film consisting of a polyester film and a modified polyester resin layer via an adhesive resin layer. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP03156287A JP3129473B2 (en) | 1991-04-04 | 1991-04-04 | Composite polyester film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP03156287A JP3129473B2 (en) | 1991-04-04 | 1991-04-04 | Composite polyester film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04307239A true JPH04307239A (en) | 1992-10-29 |
JP3129473B2 JP3129473B2 (en) | 2001-01-29 |
Family
ID=15624517
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP03156287A Expired - Fee Related JP3129473B2 (en) | 1991-04-04 | 1991-04-04 | Composite polyester film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3129473B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007517685A (en) * | 2003-12-22 | 2007-07-05 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Thermoformable polyester-containing laminate |
ITMI20121094A1 (en) * | 2012-06-21 | 2013-12-22 | Ind Termoplastica Pavese S P A | PROCESS FOR OBTAINING A MULTILAYER LAMINATE FOR THE CONSTRUCTION OF CONTAINERS, IN PARTICULAR FOR THE PACKAGING OF FOOD OR PHARMACEUTICAL PRODUCTS AND ITS LAMINATE |
CN104684733A (en) * | 2012-10-05 | 2015-06-03 | 荷兰联合利华有限公司 | Novel laminated film for packaging |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0664922U (en) * | 1993-02-23 | 1994-09-13 | タカハラ株式会社 | Loose leaf paper |
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1991
- 1991-04-04 JP JP03156287A patent/JP3129473B2/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007517685A (en) * | 2003-12-22 | 2007-07-05 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Thermoformable polyester-containing laminate |
JP4920422B2 (en) * | 2003-12-22 | 2012-04-18 | デュポン テイジン フィルムス ユーエス リミテッド パートナーシップ | Thermoformable polyester-containing laminate |
ITMI20121094A1 (en) * | 2012-06-21 | 2013-12-22 | Ind Termoplastica Pavese S P A | PROCESS FOR OBTAINING A MULTILAYER LAMINATE FOR THE CONSTRUCTION OF CONTAINERS, IN PARTICULAR FOR THE PACKAGING OF FOOD OR PHARMACEUTICAL PRODUCTS AND ITS LAMINATE |
CN104684733A (en) * | 2012-10-05 | 2015-06-03 | 荷兰联合利华有限公司 | Novel laminated film for packaging |
US10046395B2 (en) | 2012-10-05 | 2018-08-14 | Conopco, Inc. | Laminated film for packaging |
Also Published As
Publication number | Publication date |
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JP3129473B2 (en) | 2001-01-29 |
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