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WO2006087795A1 - Easy-to-tear polyester resin film - Google Patents

Easy-to-tear polyester resin film Download PDF

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Publication number
WO2006087795A1
WO2006087795A1 PCT/JP2005/002544 JP2005002544W WO2006087795A1 WO 2006087795 A1 WO2006087795 A1 WO 2006087795A1 JP 2005002544 W JP2005002544 W JP 2005002544W WO 2006087795 A1 WO2006087795 A1 WO 2006087795A1
Authority
WO
WIPO (PCT)
Prior art keywords
film
polyester resin
polyester
melting point
resin layer
Prior art date
Application number
PCT/JP2005/002544
Other languages
French (fr)
Japanese (ja)
Inventor
Kazumoto Imai
Naonobu Oda
Original Assignee
Toyo Boseki Kabushiki Kaisha
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toyo Boseki Kabushiki Kaisha filed Critical Toyo Boseki Kabushiki Kaisha
Priority to PCT/JP2005/002544 priority Critical patent/WO2006087795A1/en
Publication of WO2006087795A1 publication Critical patent/WO2006087795A1/en

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/36Layered products comprising a layer of synthetic resin comprising polyesters
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2067/00Use of polyesters or derivatives thereof, as moulding material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00Layers arrangement
    • B32B2250/24All layers being polymeric
    • B32B2250/244All polymers belonging to those covered by group B32B27/36
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/30Properties of the layers or laminate having particular thermal properties
    • B32B2307/306Resistant to heat
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/40Properties of the layers or laminate having particular optical properties
    • B32B2307/412Transparent
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/582Tearability
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2553/00Packaging equipment or accessories not otherwise provided for
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2367/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • C08J2367/02Polyesters derived from dicarboxylic acids and dihydroxy compounds

Definitions

  • the present invention relates to a stretched polyester film. More specifically, as a packaging film or tape film that maintains practical properties without losing transparency, heat resistance, barrier properties, etc. and has good tearability, or for PTP packaging and beverages
  • the present invention relates to a stretched polyester film useful as an opening for a pack.
  • cellophane has been known as a film having excellent cutting properties! Cellophane is widely used for various packaging materials and adhesive tapes due to its excellent transparency, easy cutting property, twist fixing property and the like. On the other hand, however, cellophane has a hygroscopic property, and its characteristics fluctuate depending on the season, storage condition, or atmosphere during processing, and it was difficult to always supply a product of a certain quality.
  • packaging bags and adhesive tapes using polyethylene terephthalate as a base film are used because of the excellent properties of stretched polyethylene terephthalate film such as toughness, heat resistance, water resistance, and transparency. Although it has these excellent characteristics, it has the disadvantage that it is difficult to tear the opening of a packaging bag that is difficult to cut and the adhesive tape is difficult to cut.
  • a polyester film oriented in a uniaxial direction is copolymerized with a diethylene glycol component, a low molecular weight polyester resin, or a polyester resin layer (A ) On at least one surface of the polyester resin layer (B) having a melting point higher by 10 ° C or more than the melting point of the polyester resin layer (A) and a thickness of 5% or more and 60% or less of the total thickness.
  • the laminated unstretched laminated film is heat-treated at least at a temperature lower than the melting point of the polyester resin layer (A) by at least 10 ° C. after the axial extension and at a temperature lower than the melting point of the polyester resin layer (B).
  • a method for producing a polyester film having good tearability and twistability has been proposed. (See Patent Document 1-14)
  • Patent Document 1 Japanese Patent Publication No. 55-8551
  • Patent Document 2 Japanese Patent Publication No. 56-50692
  • Patent Document 3 Japanese Patent Publication No. 55-20514
  • Patent Document 4 JP-A-5-104618
  • the method of stretching in the uniaxial direction in the above-described prior art is a method of easily cutting linearly in the alignment direction but difficult to cut in directions other than the alignment direction, and copolymerizing a large amount of diethylene glycol components and the like.
  • the method using low molecular weight polyester resin has been practically powerful because it easily causes troubles of film breakage in the stretching process.
  • the polyester resin layer (A) has a melting point higher by 10 ° C or more than the melting point of the polyester resin layer (A), and 5% or more and 60% or less of the total thickness.
  • the polyester resin layer (B) is 10 ° C. lower than the melting point of the polyester resin layer (A) at least after the unstretched laminated film having the polyester resin layer (B) having a thickness of at least uniaxially stretched.
  • the polyester resin layer (A) is brittle due to the progress of crystallization over time, and the film characteristics may change immediately after film formation and during processing. In this case, there was a failure in that the tension fluctuation during processing was broken when changing.
  • the present invention has been made against the background of the problems of the prior art, and has excellent properties of a polyester film, such as heat resistance, cold resistance, moisture resistance, transparency, fragrance retention, and easy-to-cut properties.
  • a polyester film such as heat resistance, cold resistance, moisture resistance, transparency, fragrance retention, and easy-to-cut properties.
  • tension fluctuation during processing is difficult to break when changing.
  • the present invention is a polyester film in which two or more types of polyester resin layers having different melting points are laminated, and the piercing strength is 8. ON or less and the previous A polyester-based resin film with good bow I tearability, characterized in that the tensile elongation at break in the longitudinal direction of the film is 50% or more.
  • a polyester resin layer having a melting point higher by 10 ° C. or more than the melting point of the polyester resin layer is laminated on at least one surface of the polyester resin layer, and at least uniaxial It is preferable to be stretched.
  • the polyester-based resin film according to the present invention can produce a film having excellent heat resistance, cold resistance, moisture resistance, transparency, fragrance retention, etc. and having stable and easy-cutting properties at low cost. Has the advantage.
  • the polyester resin film in the present invention is a polyester film composed of two or more polyester resin layers having different melting points, and the polyester resin layer used in each layer is crystalline. It is selected from polyester resin or amorphous polyester resin.
  • polyester resin having a higher melting point polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, or a copolymer containing these constituents as main components can be used.
  • a polyester comprising terephthalic acid as the main acid component and ethylene glycol as the main alcohol component, and more preferably a polyester comprising 95 mol% or more of terephthalic acid and 95 mol% or more of ethylene glycol.
  • the intrinsic viscosity of the above-mentioned polyethylene terephthalate! /, A copolymer mainly composed of these components, is preferably 0.55-1.3 dlZg, more preferably 0.6 0-0. 74 dlZg, particularly preferably 0.60-0.65 dlZg.
  • the polyester resin having a lower melting point includes terephthalic acid isophthalic acid-ethylene glycol copolymer, terephthalic acid ethylene glycol-neopentylglycol.
  • Polyesters containing terephthalic acid and ethylene glycol as the main components, such as a copper copolymer, and other acid components and Z or other darlicol components as copolymerization components are preferred.
  • Other acid components include aliphatic dibasic acids (eg, adipic acid, sebacic acid, azelaic acid) and aromatic dibasic acids (eg, isophthalic acid, diphenyldicarboxylic acid, 5-tert-butyl).
  • glycol component examples include aliphatic diols (for example, neopentinoglycolanol, diethylene glycol, propylene glycol, butanediol, hexanediol), alicyclic diols (for example, 1,4-cyclohexanedimethanol) or aromatics.
  • Diols for example, xylylene glycol, bis (4-j8-hydroxyphenyl) sulfone, 2,2- (4-hydroxyphenol) propane derivatives
  • the intrinsic viscosity of the copolyester is preferably 0.70-080 dlZg.
  • polyester resin layers having different melting points selected from these are laminated.
  • the layer structure of the film of the present invention is the best in the laminated structure of a layer having a high melting point and a layer having a low melting point due to film forming properties such as fusion and adhesion in the film stretching step. It is preferable that both outer layers have a high melting point.
  • the polyester resin layer of the present invention preferably has a difference in melting point of 10 ° C or more between the layer having the highest melting point and the layer having the lowest melting point, more preferably 20 °. C or higher.
  • the heat setting temperature is limited to the melting point or less of the polyester resin layer having a high melting point, if the polyester resin layer has a low melting point, sufficient heat setting cannot be performed, and the heat shrinkage rate is reduced. Is unfavorable because it increases. Therefore, polyethylene terephthalate or polyethylene naphthalate is preferred for the high melting point polyester resin layer!
  • the puncture strength is preferably 8. ON or less, more preferably 6.0. N or less, more preferably 5. ON or less. If the piercing strength exceeds 8. ON, the strength of the film will increase and it will not be possible to tear it by hand.
  • the breaking elongation in the longitudinal direction is preferably 20% or more, more preferably 50% or more. If the elongation at break is less than 20%, there is a risk of breaking due to a change in tension during processing, making stable processing difficult.
  • an elastomer component to the layer on the low melting point side so that the elongation at break in the longitudinal direction is 50% or more.
  • the elastomer component Polyolefins such as polypropylene and polyethylene that have a glass transition temperature of 20 ° C or less, polyesters that are copolymerized with polytetramethylene glycol, and the like, are copolymers of polybutylene terephthalate and polytetramethylene glycol. Is preferred.
  • the elastomer component is contained in the lower melting point layer at 1 to 5% by weight, and preferably 1 to 3% by weight!
  • the stretched film has a thickness of 9 ⁇ m force or 40 ⁇ m, but is not particularly limited.
  • the polyester film of the present invention may be added with various known additives such as a lubricant, a pigment, an antioxidant, an antistatic agent and the like within a range not inhibiting the effects of the present invention. .
  • the resin used for the polyester resin layer (A) on the side having the high and melting point and the polyester resin layer (B) having the low and melting point were prepared, respectively, and each was supplied to another two extruders. Supply, melt and extrude at temperatures above their melting points, pass through the composite adapter, and extrude from the die as a 2 type 3 layer (AZBZA), solidify by cooling, and form an unstretched laminated film.
  • AZBZA 2 type 3 layer
  • the unstretched laminated film includes a method of forming an unstretched film by extrusion from a die outlet in a state of being laminated by a coextrusion method.
  • a method of laminating unstretched films which are melted separately at a temperature equal to or higher than the melting point in a plurality of extruders and formed by extruding a die outlet force in a heated state.
  • the unstretched laminated film thus obtained is subjected to -axial stretching at a temperature not lower than the glass transition temperature of the polyester resin layer (A) and not higher than the melting point of the polyester resin layer (B). At this time The draw ratio is 2 to 30 times, preferably 9 to 16 times in terms of stretch area.
  • the stretching method may be sequential biaxial stretching or simultaneous biaxial stretching.
  • the laminated film thus obtained is heat-set at a temperature not lower than 5 ° C of the polyester resin layer (B) and lower than the melting point of the polyester resin layer (A).
  • the presence of the layer in which the molecular orientation has disappeared and the layer in which the molecular orientation has been maintained make it possible to achieve both the strength of the film and the easy-cut property, and the state of the layer configuration and heat setting. It is possible to control hand cutting by controlling.
  • JIS K 7127 “Plastic film and sheet after standing in a 50 ° C atmosphere for 3 days Measured according to “Tensile test method”.
  • Polyester resin (A) with an intrinsic viscosity of 0.62 dlZg was melted by a separate extruder at a temperature of 285 ° C. The melt was joined by a composite adapter, then extruded from a T die, and cooled by a cooling drum. Quenched to obtain a three-layer unstretched laminated film (AZBZA)
  • the unstretched laminated film was first stretched 3.8 times in the longitudinal direction at 95 ° C, then 4.0 times in the transverse direction at 110 ° C, and then relaxed by 3% and then at 220 ° C.
  • the film was heat-treated at a temperature to obtain a 16 ⁇ m film having a total thickness of layer A of 3.0 ⁇ m.
  • the obtained film had a puncture strength of 4.5 N, and was excellent in hand cutting. Table 1 shows the characteristics.
  • a film having a thickness of 16 ⁇ m was obtained by changing the total thickness of the layer A to 8 ⁇ m using the same raw materials and method as in Example 1.
  • the film obtained had a pin puncture strength of 7.2 N and excellent hand cutting properties. Table 1 shows the characteristics.
  • Example 2 Using the same raw materials and method as in Example 1, a 16 ⁇ m film was obtained in which only the thickness of layer A was changed to 12 ⁇ m. The puncture strength of the film obtained by force was 8.5 N, which was inferior to hand cutting.
  • the total thickness of the layer A was 8 ⁇ m in the same manner as in Example 1 except that the polyester resins (A) and (B) of Example 1 had the intrinsic viscosities of 0.74 and 0.76 dl / g, respectively. A 16 ⁇ m film was obtained. The puncture strength of the film obtained by caulking was 9.5 N, which was inferior to hand cutting.
  • Example 3 The same as in Example 1, except that the polyester resin layer (A) and (B) was a polyester resin having an ethylene glycol terephthalate melting point of 265 ° C and an intrinsic viscosity of 0.62 dlZg. A 16 m film was obtained. The film obtained by strengthening had a puncture strength of 10.5 N and was inferior to hand cutting.
  • polyester resin layer (B) was made of terephthalic acid, isophthalic acid-ethylene glycol, having a melting point of 221 ° C and an intrinsic viscosity of 0.664 dlZg. m films were obtained.
  • the obtained film had a significantly reduced breaking strength after being left in an atmosphere of 50 ° C.
  • Table 1 shows the evaluation results of the films obtained in Example 12 and Comparative Example 14.
  • the piercing strength is 8. ON or less, comprising a polyester film in which two or more polyester resin layers having different melting points are laminated. It can be seen that a certain polyester-based resin film has excellent hand cutting properties.
  • the polyester-based resin film of the present invention has excellent hand cutting properties, and can be used in a wide range of fields as a packaging film or tape film, or as an opening for PTP packaging or beverage packs. Can contribute to the industry.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Laminated Bodies (AREA)

Abstract

[PROBLEMS] To inexpensively provide a stretched polyester film which has satisfactory tearableness without losing strength, transparency, heat resistance, barrier properties, etc. and is useful as a packaging film or a film for tape use or as an opening material in a PTP package or beverage pack. [MEANS FOR SOLVING PROBLEMS] The easy-to-tear polyester resin film comprises two or more superposed polyester resin layers differing in melting point, and is characterized by having a piercing strength of 8.0 N or lower.

Description

明 細 書  Specification
弓 Iき裂き性の良好なポリエステル系樹脂フィルム  Bow I Polyester resin film with good tearability
技術分野  Technical field
[0001] 本発明は延伸ポリエステル系フィルムに関する。更に詳しくは、透明性、耐熱性、バ リア性等を失うことなく実用面の特性を維持し、良好な引き裂き性を具備した包装用 フィルムやテープ用フィルムとして、或 、は PTP包装や飲料のパックの開封口として 有用なポリエステル延伸フィルムに関するものである。  [0001] The present invention relates to a stretched polyester film. More specifically, as a packaging film or tape film that maintains practical properties without losing transparency, heat resistance, barrier properties, etc. and has good tearability, or for PTP packaging and beverages The present invention relates to a stretched polyester film useful as an opening for a pack.
背景技術  Background art
[0002] 従来から、切断性の優れたフィルムとしては、セロハンが知られて!/、る。セロハンは 、その優れた透明性と易切断性、ひねり固定性等の特性により各種包装材料、粘着 テープ用として重用されている。しかし、一方ではセロハンは吸湿性を有する為に特 性が季節や、保管状態、或いは加工時の雰囲気により変動し一定の品質のものを常 に供給することは困難であった。  Conventionally, cellophane has been known as a film having excellent cutting properties! Cellophane is widely used for various packaging materials and adhesive tapes due to its excellent transparency, easy cutting property, twist fixing property and the like. On the other hand, however, cellophane has a hygroscopic property, and its characteristics fluctuate depending on the season, storage condition, or atmosphere during processing, and it was difficult to always supply a product of a certain quality.
[0003] また、ポリエチレンテレフタレートをベースフィルムとした包装用袋や粘着テープな どは、延伸されたポリエチレンテレフタレートフィルムの強靭性、耐熱性、耐水性、透 明性などの優れた特性から用いられているが、これらの優れた特性を有する反面、切 断しにくぐ包装用袋の口を引き裂き難い欠点や、粘着テープが切り難い欠点があつ た。 [0003] In addition, packaging bags and adhesive tapes using polyethylene terephthalate as a base film are used because of the excellent properties of stretched polyethylene terephthalate film such as toughness, heat resistance, water resistance, and transparency. Although it has these excellent characteristics, it has the disadvantage that it is difficult to tear the opening of a packaging bag that is difficult to cut and the adhesive tape is difficult to cut.
[0004] 上記問題を解決する方法として、一軸方向に配向させたポリエステルフィルムゃジ エチレングリコール成分などを共重合させたもの、低分子量のポリエステル榭脂を用 いるもの、或いはポリエステル榭脂層(A)の少なくとも片面に、ポリエステル榭脂層( A)の融点よりも 10°C以上高い融点を有し、かつ全厚みに対し 5%以上、 60%以下 の厚みのポリエステル榭脂層(B)を積層した未延伸積層フィルムを少なくともー軸延 伸後にポリエステル榭脂層(A)の融点より 10°C低い温度以上、かつポリエステル榭 脂層(B)の融点未満の温度で熱処理することを特徴とする引き裂き性とひねり性の 良好なポリエステルフィルムの製造方法などが提案されて ヽる。(特許文献 1一 4参照 ) 特許文献 1:特公昭 55 - 8551号公報 [0004] As a method for solving the above-mentioned problem, a polyester film oriented in a uniaxial direction is copolymerized with a diethylene glycol component, a low molecular weight polyester resin, or a polyester resin layer (A ) On at least one surface of the polyester resin layer (B) having a melting point higher by 10 ° C or more than the melting point of the polyester resin layer (A) and a thickness of 5% or more and 60% or less of the total thickness. The laminated unstretched laminated film is heat-treated at least at a temperature lower than the melting point of the polyester resin layer (A) by at least 10 ° C. after the axial extension and at a temperature lower than the melting point of the polyester resin layer (B). A method for producing a polyester film having good tearability and twistability has been proposed. (See Patent Document 1-14) Patent Document 1: Japanese Patent Publication No. 55-8551
特許文献 2:特公昭 56- 50692公報  Patent Document 2: Japanese Patent Publication No. 56-50692
特許文献 3:特公昭 55— 20514公報  Patent Document 3: Japanese Patent Publication No. 55-20514
特許文献 4:特開平 5- 104618公報  Patent Document 4: JP-A-5-104618
[0005] し力しながら、上記従来技術において一軸方向に延伸させる方法は、配向方向へ は直線的に容易に切れるが配向方向以外には切れ難く、またジエチレングリコール 成分などを多量に共重合させる方法は共重合によりポリエチレンテレフタレート本来 の特性が失われるという欠点を有している。更に、低分子量のポリエステル榭脂を用 いる方法は、延伸工程での膜破れのトラブルが発生しやすくなり実用的でな力つた。  [0005] However, the method of stretching in the uniaxial direction in the above-described prior art is a method of easily cutting linearly in the alignment direction but difficult to cut in directions other than the alignment direction, and copolymerizing a large amount of diethylene glycol components and the like. Has the disadvantage that the inherent properties of polyethylene terephthalate are lost by copolymerization. In addition, the method using low molecular weight polyester resin has been practically powerful because it easily causes troubles of film breakage in the stretching process.
[0006] またポリエステル榭脂層(A)の少なくとも片面に、ポリエステル榭脂層(A)の融点よ りも 10°C以上高い融点を有し、かつ全厚みに対し 5%以上、 60%以下の厚みのポリ エステル榭脂層(B)を積層した未延伸積層フィルムを少なくとも一軸延伸後にポリェ ステル榭脂層(A)の融点より 10°C低 、温度以上、かつポリエステル榭脂層(B)の融 点未満の温度で熱処理する方法では、ポリエステル榭脂層(A)が経時による結晶化 の進行により脆ィ匕が進行し、製膜直後と加工時とでフィルムの特性の変化が生じたり 、加工時の張力変動ゃ卷替時に破断するという障害が発生した。  [0006] Further, at least one surface of the polyester resin layer (A) has a melting point higher by 10 ° C or more than the melting point of the polyester resin layer (A), and 5% or more and 60% or less of the total thickness. The polyester resin layer (B) is 10 ° C. lower than the melting point of the polyester resin layer (A) at least after the unstretched laminated film having the polyester resin layer (B) having a thickness of at least uniaxially stretched. When the heat treatment is performed at a temperature lower than the melting point of the polyester, the polyester resin layer (A) is brittle due to the progress of crystallization over time, and the film characteristics may change immediately after film formation and during processing. In this case, there was a failure in that the tension fluctuation during processing was broken when changing.
図面の簡単な説明  Brief Description of Drawings
[0007] [図 1]本発明の突刺強度測定用治具、及び測定方法 [0007] [Fig. 1] Jig strength measuring jig and measuring method of the present invention
発明の開示  Disclosure of the invention
発明が解決しょうとする課題  Problems to be solved by the invention
[0008] 本発明は従来技術の課題を背景になされたもので、ポリエステルフィルムの優れた 特性である耐熱性、耐寒性、防湿性、透明性、保香性等を有し、且つ易切断性があ り、加工時の張力変動ゃ卷替時に破断しにくい事を課題とするものである。 [0008] The present invention has been made against the background of the problems of the prior art, and has excellent properties of a polyester film, such as heat resistance, cold resistance, moisture resistance, transparency, fragrance retention, and easy-to-cut properties. However, there is a problem that tension fluctuation during processing is difficult to break when changing.
課題を解決するための手段  Means for solving the problem
[0009] 本発明者らは上記課題を解決する為、鋭意研究した結果、遂に本発明を完成する に至った。すなわち本発明は、融点の異なる 2種類以上のポリエステル榭脂層が積 層されてなるポリエステル系フィルムであって、突き刺し強度が 8. ON以下、かつ前 記フィルムの長手方向の引つ張り破断伸度が 50%以上であることを特徴とする弓 Iき 裂き性の良好なポリエステル系榭脂フィルムである。 [0009] As a result of intensive studies to solve the above problems, the present inventors have finally completed the present invention. That is, the present invention is a polyester film in which two or more types of polyester resin layers having different melting points are laminated, and the piercing strength is 8. ON or less and the previous A polyester-based resin film with good bow I tearability, characterized in that the tensile elongation at break in the longitudinal direction of the film is 50% or more.
[0010] この場合にお 、て、前記ポリエステル榭脂層の少なくとも片面に、該ポリエステル榭 脂層の融点よりも 10°C以上高い融点を有するポリエステル榭脂層を積層し、少なくと も 1軸延伸してなることが好適である。 In this case, a polyester resin layer having a melting point higher by 10 ° C. or more than the melting point of the polyester resin layer is laminated on at least one surface of the polyester resin layer, and at least uniaxial It is preferable to be stretched.
[0011] このことにより、加工時の張力変動ゃ卷替時に破断するという障害がしに《なると いう効果ある。 [0011] By this, there is an effect that the change in tension at the time of processing becomes an obstacle to breaking at the time of replacement.
発明の効果  The invention's effect
[0012] 本発明によるポリエステル系榭脂フィルムは、耐熱性、耐寒性、防湿性、透明性、 保香性等に優れ、且つ安定した易切断性を有するフィルムを安価に製造する事が出 来るという利点を有する。  [0012] The polyester-based resin film according to the present invention can produce a film having excellent heat resistance, cold resistance, moisture resistance, transparency, fragrance retention, etc. and having stable and easy-cutting properties at low cost. Has the advantage.
発明を実施するための最良の形態  BEST MODE FOR CARRYING OUT THE INVENTION
[0013] 以下、本発明を詳細に説明する。  Hereinafter, the present invention will be described in detail.
[0014] 本発明に於けるポリエステル榭脂フィルム、は融点の異なる 2種類以上のポリエステ ル榭脂層からなるポリエステル系フィルムであり、それぞれの層に使用されるポリエス テル榭脂層は、結晶性ポリエステル榭脂或いは非晶性ポリエステル榭脂より選ばれ る。  [0014] The polyester resin film in the present invention is a polyester film composed of two or more polyester resin layers having different melting points, and the polyester resin layer used in each layer is crystalline. It is selected from polyester resin or amorphous polyester resin.
[0015] 例えば、融点の高い側のポリエステノレ榭脂としては、ポリエチレンテレフタレート、ポ リブチレンテレフタレート、ポリエチレンナフタレート、あるいはそれらの構成成分を主 成分とする共重合体等が用いることができ、好ましくはテレフタル酸を主なる酸成分と し、エチレングリコールを主たるアルコール成分とするポリエステルであり、さらに好ま しくは、テレフタル酸が 95mol%以上、エチレングリコールが 95mol%以上からなる ポリエステルである。  [0015] For example, as the polyester resin having a higher melting point, polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, or a copolymer containing these constituents as main components can be used. Is a polyester comprising terephthalic acid as the main acid component and ethylene glycol as the main alcohol component, and more preferably a polyester comprising 95 mol% or more of terephthalic acid and 95 mol% or more of ethylene glycol.
なお、上記ポリエチレンテレフタレートある!/、はそれらの構成成分を主成分とする共 重合体等の固有粘度は、好ましくは 0. 55- 1. 3dlZgであり、さらに好ましくは 0. 6 0-0. 74dlZgであり、特に好ましくは 0. 60-0. 65dlZgである。  The intrinsic viscosity of the above-mentioned polyethylene terephthalate! /, A copolymer mainly composed of these components, is preferably 0.55-1.3 dlZg, more preferably 0.6 0-0. 74 dlZg, particularly preferably 0.60-0.65 dlZg.
[0016] また、融点の低!、方のポリエステル榭脂としては、テレフタル酸 イソフタル酸ーェチ レングリコール共重合体、テレフタル酸 エチレングリコールーネォペンチルグリコー ル共重合体等のテレフタル酸およびエチレングリコールを主成分とし、他の酸成分お よび Zまたは他のダリコール成分を共重合成分として含有するポリエステルが好まし い。他の酸成分としては、脂肪族の二塩基酸 (例えば、アジピン酸、セバチン酸、ァ ゼライン酸)や芳香族の二塩基酸(例えば、イソフタル酸、ジフヱ-ルジカルボン酸、 5 —第 3ブチルイソフタル酸、 2, 2, 6, 6—テトラメチルビフエ-ルー 4, 4ージカルボン酸、 2, 6 ナフタレンジカルボン酸、 1, 1, 3—トリメチルー 3 フエ-ルインデン 4, 5—ジカ ルボン酸)が用いられる。グリコール成分としては、脂肪族ジオール (例えば、ネオペ ンチノレグリコーノレ、ジエチレングリコール、プロピレングリコール、ブタンジオール、へ キサンジオール)、脂環族ジオール (例えば、 1, 4ーシクロへキサンジメタノール)また は芳香族ジオール(例えば、キシリレングリコール、ビス(4— j8—ヒドロキシフエ-ル)ス ルホン、 2, 2— (4—ヒドロキシフエ-ル)プロパン誘導体)が用いられる。 [0016] In addition, the polyester resin having a lower melting point includes terephthalic acid isophthalic acid-ethylene glycol copolymer, terephthalic acid ethylene glycol-neopentylglycol. Polyesters containing terephthalic acid and ethylene glycol as the main components, such as a copper copolymer, and other acid components and Z or other darlicol components as copolymerization components are preferred. Other acid components include aliphatic dibasic acids (eg, adipic acid, sebacic acid, azelaic acid) and aromatic dibasic acids (eg, isophthalic acid, diphenyldicarboxylic acid, 5-tert-butyl). Isophthalic acid, 2, 2, 6, 6-tetramethylbiphenyl 4,4-dicarboxylic acid, 2,6 naphthalenedicarboxylic acid, 1, 1,3-trimethyl-3-phenolindene 4,5-dicarboxylic acid) Used. Examples of the glycol component include aliphatic diols (for example, neopentinoglycolanol, diethylene glycol, propylene glycol, butanediol, hexanediol), alicyclic diols (for example, 1,4-cyclohexanedimethanol) or aromatics. Diols (for example, xylylene glycol, bis (4-j8-hydroxyphenyl) sulfone, 2,2- (4-hydroxyphenol) propane derivatives) are used.
なお、上記共重合ポリエステルの固有粘度は、好ましくは 0. 70— 080dlZgである のが好ましい。  The intrinsic viscosity of the copolyester is preferably 0.70-080 dlZg.
[0017] これらの内より選ばれた融点の異なる 2種類以上のポリエステル榭脂層が積層され てなることが好ましい。  [0017] It is preferable that two or more types of polyester resin layers having different melting points selected from these are laminated.
[0018] さらに、本発明のフィルムの層構成は、フィルムの延伸工程での融着、粘着等の製 膜性より、融点の高い層と融点の低い層の積層構成に於いて、フィルムの最外層を 共に融点の高 、層とすることが好ま 、。  [0018] Furthermore, the layer structure of the film of the present invention is the best in the laminated structure of a layer having a high melting point and a layer having a low melting point due to film forming properties such as fusion and adhesion in the film stretching step. It is preferable that both outer layers have a high melting point.
[0019] 又、本発明のポリエステル榭脂層は、最も高い融点を示す層と、最も低い融点を示 す層の融点の差が 10°C以上である事が好ましぐさらに好ましくは 20°C以上である。  [0019] The polyester resin layer of the present invention preferably has a difference in melting point of 10 ° C or more between the layer having the highest melting point and the layer having the lowest melting point, more preferably 20 °. C or higher.
[0020] 該融点差が 10°C未満の場合、製膜工程に於いて、低融点のポリエステル榭脂層 の配向を崩壊させる為に、該榭脂層の融点以上の温度に曝した際に、高融点のポリ エステル榭脂層が軟ィ匕或いは溶融して、製膜が不安定となる。  [0020] When the difference between the melting points is less than 10 ° C, in order to disrupt the orientation of the low-melting polyester resin layer in the film-forming process, when exposed to a temperature higher than the melting point of the resin layer. The high melting point polyester resin layer becomes soft or melts and the film formation becomes unstable.
[0021] 更に、熱固定の温度が高融点のポリエステル榭脂層の融点以下に限定される為、 該ポリエステル榭脂層の融点が低いと充分な熱固定を行なうことができず、熱収縮率 が大きくなり好ましくない。従って高融点ポリエステル榭脂層としては、ポリエチレンテ レフタレート、又はポリエチレンナフタレートが好まし!/、。  [0021] Further, since the heat setting temperature is limited to the melting point or less of the polyester resin layer having a high melting point, if the polyester resin layer has a low melting point, sufficient heat setting cannot be performed, and the heat shrinkage rate is reduced. Is unfavorable because it increases. Therefore, polyethylene terephthalate or polyethylene naphthalate is preferred for the high melting point polyester resin layer!
[0022] 本発明に於いて、突刺強度は 8. ON以下であることが好ましぐ更に好ましくは 6. 0 N以下であり、より好ましくは 5. ON以下である。突刺強度が 8. ONを越える場合、フ イルムの強度が強くなり、手で引き裂くことができなくなり好ましくない。 [0022] In the present invention, the puncture strength is preferably 8. ON or less, more preferably 6.0. N or less, more preferably 5. ON or less. If the piercing strength exceeds 8. ON, the strength of the film will increase and it will not be possible to tear it by hand.
[0023] 本発明に於いて、長手方向の破断伸度は 20%以上であることが好ましぐ 50%以 上であることがより好ましい。破断伸度が 20%未満の場合、加工時の張力変化により 破断することが危惧され、安定した加工が困難となる。  [0023] In the present invention, the breaking elongation in the longitudinal direction is preferably 20% or more, more preferably 50% or more. If the elongation at break is less than 20%, there is a risk of breaking due to a change in tension during processing, making stable processing difficult.
[0024] 本発明に於いて、長手方向の破断伸度を 50%以上とする為に、低融点側の層に エラストマ一成分を添加する事が好ましい、この場合のエラストマ一成分としては、ガ ラス転移温度が 20°C以下であるものが好ましぐポリプロピレン、ポリエチレン等のポ リオレフインや、ポリテトラメチレングリコールを共重合したポリエステル等があげられ、 ポリブチレンテレフタレートとポリテトラメチレングリコールの共重合体が好ましい。 エラストマ一成分は低融点側の層に 1一 5重量%含まれるのが好ましぐさらに 1一 3 重量%であることが好まし!/、。  In the present invention, it is preferable to add an elastomer component to the layer on the low melting point side so that the elongation at break in the longitudinal direction is 50% or more. In this case, as the elastomer component, Polyolefins such as polypropylene and polyethylene that have a glass transition temperature of 20 ° C or less, polyesters that are copolymerized with polytetramethylene glycol, and the like, are copolymers of polybutylene terephthalate and polytetramethylene glycol. Is preferred. It is preferable that the elastomer component is contained in the lower melting point layer at 1 to 5% by weight, and preferably 1 to 3% by weight!
[0025] 本発明に於 、て、延伸フィルムの厚みは包装用袋や粘着テープなどで使用される フィルムの厚みは 9 μ m力ら 40 μ mであるが、特に限定されるものではない。  In the present invention, the stretched film has a thickness of 9 μm force or 40 μm, but is not particularly limited.
[0026] 本発明のポリエステルフィルムは、本発明の効果を阻害しな ヽ範囲で、公知の各種 添加材、例えば、滑材、顔料、酸化防止剤、帯電防止剤等が添加されていてもよい。  [0026] The polyester film of the present invention may be added with various known additives such as a lubricant, a pigment, an antioxidant, an antistatic agent and the like within a range not inhibiting the effects of the present invention. .
[0027] 次に、本発明フィルムの製造方法の一例を説明する。  [0027] Next, an example of a method for producing the film of the present invention will be described.
[0028] 高 、融点を有する側のポリエステル榭脂層(A)及び低 、融点を有するポリエステ ル榭脂層(B)に用いる榭脂をそれぞれ調製し、それぞれを別の 2台の押出機に供給 し、それぞれの融点以上の温度で溶融押し出しし、複合アダプターを通過させ、 2種 3層(AZBZA)として口金より押し出し冷却固化させて未延伸積層フィルムを成形 する。  [0028] The resin used for the polyester resin layer (A) on the side having the high and melting point and the polyester resin layer (B) having the low and melting point were prepared, respectively, and each was supplied to another two extruders. Supply, melt and extrude at temperatures above their melting points, pass through the composite adapter, and extrude from the die as a 2 type 3 layer (AZBZA), solidify by cooling, and form an unstretched laminated film.
[0029] ここでいう未延伸積層フィルムとは、共押出し法により積層した状態でダイス出口よ り押 出して未延伸フィルムを成形する方法が挙げられる。別の方法としては、複数 の押出機の中で、融点以上の温度で別々に溶融し、ダイス出口力 押し出して成形 した未延伸フィルム同士を加温状態でラミネートする方法がある。  [0029] As used herein, the unstretched laminated film includes a method of forming an unstretched film by extrusion from a die outlet in a state of being laminated by a coextrusion method. As another method, there is a method of laminating unstretched films which are melted separately at a temperature equal to or higher than the melting point in a plurality of extruders and formed by extruding a die outlet force in a heated state.
[0030] このように得られた未延伸積層フィルムをポリエステル榭脂層(A)のガラス転移温 度以上、ポリエステル榭脂層(B)の融点以下の温度で-軸延伸を行なう。この際の 延伸倍率は延伸面積で 2— 30倍、好ましくは 9一 16倍である。また延伸方式は逐次 二軸延伸でも同時二軸延伸でもよい。 [0030] The unstretched laminated film thus obtained is subjected to -axial stretching at a temperature not lower than the glass transition temperature of the polyester resin layer (A) and not higher than the melting point of the polyester resin layer (B). At this time The draw ratio is 2 to 30 times, preferably 9 to 16 times in terms of stretch area. The stretching method may be sequential biaxial stretching or simultaneous biaxial stretching.
[0031] このように得られた積層フィルムをポリエステル榭脂層(B)の融点 5°C以上、ポリエ ステル榭脂層(A)の融点未満の温度で熱固定を行なう。 [0031] The laminated film thus obtained is heat-set at a temperature not lower than 5 ° C of the polyester resin layer (B) and lower than the melting point of the polyester resin layer (A).
[0032] 本発明では、分子配向が消失した層と、分子配向を維持した層が存在することで、 フィルムの強度と易カット性を両立させることができ、また、層構成や熱固定の状態を 制御することで手切れ性をコントロールすることができる。 [0032] In the present invention, the presence of the layer in which the molecular orientation has disappeared and the layer in which the molecular orientation has been maintained make it possible to achieve both the strength of the film and the easy-cut property, and the state of the layer configuration and heat setting. It is possible to control hand cutting by controlling.
[0033] 本発明では、突刺強度が 8. ON以下とすることにより、生産'加工性に優れ、且つ 優れた引き裂き性を有するフィルムが得られる。 [0033] In the present invention, when the puncture strength is 8. ON or less, a film having excellent production processability and excellent tearability can be obtained.
実施例  Example
[0034] 次に実施例、及び比較例を用いて本発明を具体的に説明する。実施例および比 較例における評価の方法にっ 、ては (a)及び (b)の方法で行った。  Next, the present invention will be specifically described with reference to examples and comparative examples. The evaluation methods in Examples and Comparative Examples were carried out by the methods (a) and (b).
[0035] (A)突刺強度 [0035] (A) Puncture strength
長手方向 200mm、幅方向 20mmの試料を切り出す。引張試験機(島津製作所製 オートグラフ AGC— 1KNG型)を用い、試料を 2つ折として、チャックからの長さが 50 mmとなるようにチャックに挟む。折り返し部分を直径 0. 7mmの鋼球が突き刺すよう に、 50mmZminの速度にて引っ張り、突き刺して穴を開けた時の荷重を求める。測 定は n= 5行 、、最高値と最低値を除!、た 3点の平均にて求めた。  Cut out a specimen with a length of 200 mm and a width of 20 mm. Using a tensile tester (manufactured by Shimadzu Corporation, Autograph AGC-1KNG type), fold the sample in half so that the length from the chuck is 50 mm. Pull at a speed of 50mmZmin so that a steel ball with a diameter of 0.7mm will pierce the folded part, and determine the load when the hole is pierced. Measurements were made with an average of 3 points, n = 5 lines, excluding the highest and lowest values!
[0036] (b)手切れ性 [0036] (b) Hand cutting
官能テストで行、、当該ポリエステルフィルム ZZ9 μ mアルミニウム箔 Z15 m押 出し LDPEとラミネートして積層体を作成した後、ヒートシールにて製袋し、シール部 分を手で切断した時の開封性で評価した。尚、袋を両手で持つ際には、 3mm程度 の間隔を持ち、長手方向、幅方向の両方で行った。  Performed by sensory test, the polyester film ZZ9 μm aluminum foil Z15 m extruded Laminate by laminating with LDPE, then bag-making with heat seal, and unsealing when the seal part is cut by hand It was evaluated with. In addition, when holding the bag with both hands, there was an interval of about 3 mm, and it was performed both in the longitudinal direction and in the width direction.
〇:爪を立てることなく容易に開封できる  ○: Can be opened easily without raising nails
△:爪を立てることで容易に開封できる  Δ: Can be easily opened by raising nails
X:爪を立てても容易に開封できない  X: Cannot be opened easily even if the nails are raised
[0037] (c)長手方向の引っ張り破断伸度 [0037] (c) Longitudinal tensile elongation at break
50°C雰囲気下に 3日間放置した後、 JIS K 7127「プラスチックフィルム及びシート の引張試験方法」に準じて測定した。 JIS K 7127 “Plastic film and sheet after standing in a 50 ° C atmosphere for 3 days Measured according to “Tensile test method”.
[0038] (実施例 1)  [0038] (Example 1)
テレフタル酸 イソフタル酸ーエチレングリコールカゝらなる、融点が 221°C、極限粘度 0. 64dlZgのポリエステル榭脂 98重量0 /0と、テレフタル酸 エチレングリコール ポリ テトラメチレングリコール力もなる、融点が 170°C、極限粘度 0. 76dlZgのエラストマ 一 2重量%からなる層(B)とテレフタル酸 エチレングリコール力もなる、融点が 265 。C、極限粘度 0. 62dlZgのポリエステル榭脂(A)を、おのおの 285°Cの温度で別々 の押出し機により溶融し、この溶融体を複合アダプターで合流させた後に Tダイより 押出し、冷却ドラムで急冷して (AZBZA)構成の 3層の未延伸積層フィルムを得た Terephthalic acid isophthalic acid-ethylene glycol mosquitoゝRanaru, melting point 221 ° C, the polyester榭脂98 weight 0/0 of intrinsic viscosity 0. 64DlZg, also terephthalic acid ethylene glycol polytetramethylene glycol force, melting point 170 ° C A layer (B) consisting of an elastomer with an intrinsic viscosity of 0.76 dlZg, 1% by weight, and an ethylene glycol terephthalate, melting point 265. C. Polyester resin (A) with an intrinsic viscosity of 0.62 dlZg was melted by a separate extruder at a temperature of 285 ° C. The melt was joined by a composite adapter, then extruded from a T die, and cooled by a cooling drum. Quenched to obtain a three-layer unstretched laminated film (AZBZA)
[0039] 該未延伸積層フィルムを先ず縦方向に 95°Cで 3. 8倍、次いで横方向に 110°Cで 4 . 0倍に延伸した後、 3%の弛緩を行ないつつ 220°Cの温度で熱処理を行い、 A層の 厚みの合計が 3. 0 μ mである 16 μ mのフィルムを得た。得られたフィルムの突刺強 度は 4. 5Nであり、手切れ性に優れていた。特性を表 1に示す。 [0039] The unstretched laminated film was first stretched 3.8 times in the longitudinal direction at 95 ° C, then 4.0 times in the transverse direction at 110 ° C, and then relaxed by 3% and then at 220 ° C. The film was heat-treated at a temperature to obtain a 16 μm film having a total thickness of layer A of 3.0 μm. The obtained film had a puncture strength of 4.5 N, and was excellent in hand cutting. Table 1 shows the characteristics.
[0040] (実施例 2)  [0040] (Example 2)
実施例 1と同じ原料、方法で A層の厚みの合計が 8 μ mに変更した 16 μ mのフィル ムを得た。得られたフィルムの得られたフィルムの突刺強度は 7. 2Nであり、手切れ 性に優れていた。特性を表 1に示す。  A film having a thickness of 16 μm was obtained by changing the total thickness of the layer A to 8 μm using the same raw materials and method as in Example 1. The film obtained had a pin puncture strength of 7.2 N and excellent hand cutting properties. Table 1 shows the characteristics.
[0041] (比較例 1) [0041] (Comparative Example 1)
実施例 1と同じ原料、方法で、 A層の厚みのみ 12 μ mに変更した 16 μ mのフィルム を得た。力べして得られたフィルムの突刺強度は 8. 5Nであり、手切れ性に劣ってい た。  Using the same raw materials and method as in Example 1, a 16 μm film was obtained in which only the thickness of layer A was changed to 12 μm. The puncture strength of the film obtained by force was 8.5 N, which was inferior to hand cutting.
[0042] (比較例 2)  [0042] (Comparative Example 2)
実施例 1のポリエステル榭脂 (A)、 (B)の極限粘度をそれぞれ、 0. 74、 0. 76dl/ gとした以外は実施例 1と同様な方法で A層の厚みの合計が 8 μ mである 16 μ mのフ イルムを得た。カゝくして得られたフィルムの突刺強度は 9. 5Nであり、手切れ性に劣つ ていた。  The total thickness of the layer A was 8 μm in the same manner as in Example 1 except that the polyester resins (A) and (B) of Example 1 had the intrinsic viscosities of 0.74 and 0.76 dl / g, respectively. A 16 μm film was obtained. The puncture strength of the film obtained by caulking was 9.5 N, which was inferior to hand cutting.
[0043] (比較例 3) ポリエステル榭脂層(A)、及び (B)として、テレフタル酸 エチレングリコール力ゝらな る融点が 265°C、極限粘度 0. 62dlZgのポリエステル榭脂を用いた以外は、実施例 1と同様に 16 mのフィルムを得た。力くして得られたフィルムは、突刺強度が 10. 5 Nであり、手切れ性に劣っていた。 [0043] (Comparative Example 3) The same as in Example 1, except that the polyester resin layer (A) and (B) was a polyester resin having an ethylene glycol terephthalate melting point of 265 ° C and an intrinsic viscosity of 0.62 dlZg. A 16 m film was obtained. The film obtained by strengthening had a puncture strength of 10.5 N and was inferior to hand cutting.
[0044] (比較例 4) [0044] (Comparative Example 4)
ポリエステル榭脂層(B)として、テレフタル酸 イソフタル酸ーエチレングリコールか らなる、融点が 221°C、極限粘度 0. 64dlZgのポリエステル榭脂を用いた以外は実 施例 1と同様にして 16 μ mのフィルムを得た。得られたフィルムは 50°C雰囲気下に 放置した後、破断強度が著しく低下していた。  16 μm in the same manner as in Example 1 except that the polyester resin layer (B) was made of terephthalic acid, isophthalic acid-ethylene glycol, having a melting point of 221 ° C and an intrinsic viscosity of 0.664 dlZg. m films were obtained. The obtained film had a significantly reduced breaking strength after being left in an atmosphere of 50 ° C.
[0045] 実施例 1 2、比較例 1 4で得られたフィルムの評価結果を表 1に示す。  [0045] Table 1 shows the evaluation results of the films obtained in Example 12 and Comparative Example 14.
[0046] [表 1]  [0046] [Table 1]
Figure imgf000009_0001
Figure imgf000009_0001
[0047] 実施例 1 2、比較例 1 3より明らかなように、融点の異なる 2種類以上のポリエステ ル榭脂層が積層されてなるポリエステル系フィルムよりなる、突き刺し強度が 8. ON以 下であるポリエステル系榭脂フィルムは、優れた手切れ性を有することが解る。  [0047] As is clear from Example 1 2 and Comparative Example 1 3, the piercing strength is 8. ON or less, comprising a polyester film in which two or more polyester resin layers having different melting points are laminated. It can be seen that a certain polyester-based resin film has excellent hand cutting properties.
産業上の利用可能性  Industrial applicability
[0048] 本発明のポリエステル系榭脂フィルムは、優れた手切れ性を有し、包装用フィルム やテープ用フィルムとして、或いは PTP包装や飲料のパックの開封口として幅広い用 途分野に利用する事ができ、産業界に寄与する事が大である。 [0048] The polyester-based resin film of the present invention has excellent hand cutting properties, and can be used in a wide range of fields as a packaging film or tape film, or as an opening for PTP packaging or beverage packs. Can contribute to the industry.

Claims

請求の範囲 The scope of the claims
[1] 融点の異なる、少なくとも 2種類以上のポリエステル榭脂層が積層されてなるポリエ ステル系フィルムであって、突き刺し強度が 8. ON以下、かつ前記フィルムの長手方 向の引っ張り破断伸度が 50%以上であることを特徴とする引き裂き性の良好なポリ エステル系榭脂フィルム。  [1] A polyester film in which at least two types of polyester resin layers having different melting points are laminated, the piercing strength is 8. ON or less, and the tensile breaking elongation in the longitudinal direction of the film is Polyester-based resin film having good tearability, characterized by being 50% or more.
[2] 請求項 1に記載の引き裂き性の良好なポリエステル系榭脂フィルムであって、前記 ポリエステル榭脂層の少なくとも片面に、該ポリエステル榭脂層の融点よりも 10°C以 上高い融点を有するポリエステル榭脂層を積層した、少なくとも 1軸延伸してなること を特徴とする弓 Iき裂き性の良好なポリエステル系榭脂フィルム。  [2] A polyester-based resin film having good tearability according to claim 1, wherein at least one surface of the polyester resin layer has a melting point higher by 10 ° C or more than the melting point of the polyester resin layer. A polyester-based resin film having good bow I cracking characteristics, wherein the polyester resin-coated layer is laminated and is stretched at least uniaxially.
PCT/JP2005/002544 2005-02-18 2005-02-18 Easy-to-tear polyester resin film WO2006087795A1 (en)

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Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05104618A (en) * 1991-10-17 1993-04-27 Toyobo Co Ltd Manufacture for polyester film having favorable tear property and twisting property
WO1994029374A1 (en) * 1993-06-10 1994-12-22 Nkk Corporation Film formed from polyethylene 2,6-naphthalate resin, process for producing said film, and wrapping using said film
JP2002337290A (en) * 2001-05-16 2002-11-27 Toyobo Co Ltd Laminated polyester film
JP2002337285A (en) * 2001-05-16 2002-11-27 Toyobo Co Ltd Laminated polyester film
JP2003311905A (en) * 2002-04-24 2003-11-06 Toyobo Co Ltd Stretched polyester film
JP2003311904A (en) * 2002-04-24 2003-11-06 Toyobo Co Ltd Stretched polyester film and method for manufacturing it
JP2003311906A (en) * 2002-04-24 2003-11-06 Toyobo Co Ltd Stretched polyester film
JP2004098571A (en) * 2002-09-11 2004-04-02 Toyobo Co Ltd Polyester film and its manufacturing method
JP2004358798A (en) * 2003-06-04 2004-12-24 Unitika Ltd Laminated biaxially stretched polyester film excellent in easy cutting properties

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05104618A (en) * 1991-10-17 1993-04-27 Toyobo Co Ltd Manufacture for polyester film having favorable tear property and twisting property
WO1994029374A1 (en) * 1993-06-10 1994-12-22 Nkk Corporation Film formed from polyethylene 2,6-naphthalate resin, process for producing said film, and wrapping using said film
JP2002337290A (en) * 2001-05-16 2002-11-27 Toyobo Co Ltd Laminated polyester film
JP2002337285A (en) * 2001-05-16 2002-11-27 Toyobo Co Ltd Laminated polyester film
JP2003311905A (en) * 2002-04-24 2003-11-06 Toyobo Co Ltd Stretched polyester film
JP2003311904A (en) * 2002-04-24 2003-11-06 Toyobo Co Ltd Stretched polyester film and method for manufacturing it
JP2003311906A (en) * 2002-04-24 2003-11-06 Toyobo Co Ltd Stretched polyester film
JP2004098571A (en) * 2002-09-11 2004-04-02 Toyobo Co Ltd Polyester film and its manufacturing method
JP2004358798A (en) * 2003-06-04 2004-12-24 Unitika Ltd Laminated biaxially stretched polyester film excellent in easy cutting properties

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