JP2661427B2 - Heat fusion method of container body - Google Patents

Heat fusion method of container body

Info

Publication number
JP2661427B2
JP2661427B2 JP3216037A JP21603791A JP2661427B2 JP 2661427 B2 JP2661427 B2 JP 2661427B2 JP 3216037 A JP3216037 A JP 3216037A JP 21603791 A JP21603791 A JP 21603791A JP 2661427 B2 JP2661427 B2 JP 2661427B2
Authority
JP
Japan
Prior art keywords
polyester
polyolefin
heat
acid
hot air
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.)
Expired - Fee Related
Application number
JP3216037A
Other languages
Japanese (ja)
Other versions
JPH0531832A (en
Inventor
賢次 林
浩哉 志岐
秀樹 山本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toppan Inc
Original Assignee
Toppan Printing Co Ltd
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 Toppan Printing Co Ltd filed Critical Toppan Printing Co Ltd
Priority to JP3216037A priority Critical patent/JP2661427B2/en
Priority to DE69207843T priority patent/DE69207843T2/en
Priority to EP92112987A priority patent/EP0529336B1/en
Publication of JPH0531832A publication Critical patent/JPH0531832A/en
Application granted granted Critical
Publication of JP2661427B2 publication Critical patent/JP2661427B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C65/00Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
    • B29C65/02Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
    • B29C65/10Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using hot gases (e.g. combustion gases) or flames coming in contact with at least one of the parts to be joined
    • B29C65/103Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using hot gases (e.g. combustion gases) or flames coming in contact with at least one of the parts to be joined direct heating both surfaces to be joined
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/02Preparation of the material, in the area to be joined, prior to joining or welding
    • B29C66/028Non-mechanical surface pre-treatments, i.e. by flame treatment, electric discharge treatment, plasma treatment, wave energy or particle radiation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/05Particular design of joint configurations
    • B29C66/10Particular design of joint configurations particular design of the joint cross-sections
    • B29C66/11Joint cross-sections comprising a single joint-segment, i.e. one of the parts to be joined comprising a single joint-segment in the joint cross-section
    • B29C66/112Single lapped joints
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/05Particular design of joint configurations
    • B29C66/10Particular design of joint configurations particular design of the joint cross-sections
    • B29C66/13Single flanged joints; Fin-type joints; Single hem joints; Edge joints; Interpenetrating fingered joints; Other specific particular designs of joint cross-sections not provided for in groups B29C66/11 - B29C66/12
    • B29C66/135Single hemmed joints, i.e. one of the parts to be joined being hemmed in the joint area
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/40General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
    • B29C66/41Joining substantially flat articles ; Making flat seams in tubular or hollow articles
    • B29C66/43Joining a relatively small portion of the surface of said articles
    • B29C66/432Joining a relatively small portion of the surface of said articles for making tubular articles or closed loops, e.g. by joining several sheets ; for making hollow articles or hollow preforms
    • B29C66/4326Joining a relatively small portion of the surface of said articles for making tubular articles or closed loops, e.g. by joining several sheets ; for making hollow articles or hollow preforms for making hollow articles or hollow-preforms, e.g. half-shells
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/71General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/723General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/73General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/739General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of the parts to be joined being a thermoplastic or a thermoset
    • B29C66/7392General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of at least one of the parts being a thermoplastic
    • B29C66/73921General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the material of at least one of the parts being a thermoplastic characterised by the materials of both parts being thermoplastics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/723General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered
    • B29C66/7232General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a non-plastics layer
    • B29C66/72321General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a non-plastics layer consisting of metals or their alloys
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/723General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered
    • B29C66/7232General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a non-plastics layer
    • B29C66/72327General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a non-plastics layer consisting of natural products or their composites, not provided for in B29C66/72321 - B29C66/72324
    • B29C66/72328Paper
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/72General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
    • B29C66/723General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered
    • B29C66/7234General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a barrier layer
    • B29C66/72341General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered comprising a barrier layer for gases

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は容器用構成材料の熱融着
方法に関し、更に詳しくは、ポリオレフィン部分とポリ
エステル部分からなる表面とポリエステル表面を同時に
熱融着する方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for heat-sealing a container material, and more particularly, to a method for simultaneously heat-sealing a polyester surface and a surface comprising a polyolefin portion and a polyester portion.

【0002】[0002]

【従来の技術】乳飲料、果実飲料、酒等の液体飲料用容
器としては、その衛生性、耐水性、防湿性及び熱封緘が
可能である事等から、従来、紙を基材とし、内面をポリ
オレフィン類等で加工した容器構成材料が用いられてい
る。
2. Description of the Related Art Containers for liquid drinks such as milk drinks, fruit drinks, and sake are conventionally made of paper as a base material because of their hygiene, water resistance, moisture proofness, and heat sealability. Of the container is processed by using a polyolefin or the like.

【0003】このような容器構成材料のうち、例えば図
3に示されるような胴部を有する容器においては、特に
内容物が酒等の場合、その接合部は構成材料端面が容器
内部に露出して内容物に接触することのないように構成
されている。すなわち、図3Aで示す部分は、図4に拡
大断面図として示すように、一方の材料端部を接着に必
要な所定長さで内側に折り曲げ、該折り曲げ部分の外面
とこれに対応する他方の材料端部の内面とを接着させる
際、予め、前記折り曲げ部分に相当する部分の先端から
厚み方向の中心付近、すなわち、紙の部分の外側部分を
先端から一定長さで除去し、残った内側の半分の厚み部
分を外側の除去部分へ折りこんでおく方法が通常用いら
れている。従って、Xで示される部分においては構成材
料の内面同志が接着され、Yで示される部分においては
構成材料の外面と内面が接着されることになる。
[0003] Among such container constituent materials, in a container having a body as shown in FIG. 3, for example, especially when the contents are sake or the like, the joint portion is formed such that the end face of the constituent material is exposed inside the container. It does not come into contact with the contents. That is, as shown in an enlarged sectional view in FIG. 4, the portion shown in FIG. 3A is formed by bending one end of the material inward at a predetermined length required for bonding, and the outer surface of the bent portion and the other corresponding surface are bent. When bonding the inner surface of the material end portion, in advance, the vicinity of the center in the thickness direction from the tip of the portion corresponding to the bent portion, that is, the outer portion of the paper portion is removed from the tip at a fixed length, and the remaining inner portion is removed. A method of folding a half-thick portion into an outer removed portion is usually used. Therefore, at the portion indicated by X, the inner surfaces of the constituent materials are bonded together, and at the portion indicated by Y, the outer surface and the inner surface of the constituent material are bonded.

【0004】従来、前記の如き容器構成材料としては、
内面、外面のいずれもポリオレフィンが用いられてい
た。しかしながら容器内面にポリオレフィンを用いた場
合、ポリオレフィンが飲料の香味成分を吸着又は透過す
るという性質を有しているため、飲料本来の香り、味等
が維持されないという問題があり、更に上記材料をポリ
オレフィンの押出コーティングにより作成する場合、樹
脂の酸化がおこりやすく、このため異臭が発生するとい
う問題も生じていた。
[0004] Conventionally, as a container constituting material as described above,
Polyolefin was used for both the inner surface and the outer surface. However, when a polyolefin is used for the inner surface of the container, the polyolefin has a property of adsorbing or permeating a flavor component of the beverage, and thus there is a problem that the original aroma and taste of the beverage are not maintained. In the case where the resin is prepared by extrusion coating, there is a problem that the resin is easily oxidized, thereby generating an unpleasant odor.

【0005】上記問題点を解決するために、近年容器内
面層としてポリオレフィンのかわりにポリエステル、特
にヒートシール性に優れたポリエステルを用いたものが
容器構成材料として用いられている。
In order to solve the above-mentioned problems, in recent years, instead of polyolefin, polyester, particularly polyester having excellent heat sealing properties, has been used as a container constituting material instead of polyolefin as an inner surface layer of the container.

【0006】[0006]

【発明が解決しようとする課題】上記の如くヒートシー
ル性ポリエステルを用いた場合においても、紙を主体と
した構成材料の場合、端部の接着部分を形成するためヒ
ートシールを行なおうとしても、紙が断熱材として作用
するため、現実には熱融着は困難であった。このため、
熱融着させるべき両方の面をガスバーナー等であぶり、
加熱溶融した後、重ねあわせ融着する、いわゆるフレー
ム処理が行なわれるが、前記の如く、一方の表面が二種
以上の材質、即ち、ポリエステル部分とポリオレフィン
部分を有する場合、フレーム処理により、ポリエステル
表面に低級酸化物が生成し、該酸化物がポリエステル同
志の接着を阻害するため、図4におけるXの部分の接着
が不十分であった。
In the case where the heat-sealable polyester is used as described above, in the case of a material mainly composed of paper, even if heat sealing is performed to form an adhesive portion at the end. However, since the paper acts as a heat insulating material, it is actually difficult to perform heat fusion. For this reason,
Both surfaces to be heat-sealed are burned with a gas burner or the like,
After being heated and melted, a so-called flame treatment of superimposing and fusing is performed. As described above, when one surface has two or more materials, that is, a polyester portion and a polyolefin portion, the polyester surface is treated by the flame treatment. In this case, a lower oxide was formed, and the oxide hindered the adhesion between the polyesters. Therefore, the adhesion at the portion X in FIG. 4 was insufficient.

【0007】従って、本発明の目的は、ポリオレフィン
部分とポリエステル部分からなる表面とポリエステル表
面とを同時に良好な接着強度をもって熱融着しうる方法
を提供することにある。
Accordingly, it is an object of the present invention to provide a method capable of simultaneously heat-sealing a surface comprising a polyolefin portion and a polyester portion and a polyester surface with good adhesive strength.

【0008】[0008]

【課題を解決するための手段】本発明者等は、前記課題
に鑑みて、鋭意研究の結果、本発明の上記目的は、基体
上の一方の面側にポリオレフィン表面層を有し、他方の
面側にポリエステル表面層を有する積層体フィルムの前
記ポリエステル表面層の一方の端部を前記ポリオレフィ
ン表面層側に折り返して形成されたポリオレフィン部分
とポリエステル部分からなる表面を有する端部と、他方
の面側のポリエステル表面層の端部とを熱融着する容器
胴部の熱融着方法であり、前記ポリオレフィン部分と前
記ポリエステル部分からなる表面を有する端部の前記ポ
リオレフィン部分の表面をフレーム処理すると共に前記
ポリエステル部分の表面をホットエアー処理し、他方の
面側のポリエステル表面層の端部をホットエアー処理
し、次いで両端部のそれぞれの表面を互いに圧着して熱
融着することを特徴とする容器胴部の熱融着方法により
達成されることを見出した。また、前記ポリオレフィン
部分及びポリエステル部分からなる表面のポリオレフィ
ン部分をフレーム処理した後にポリエステル部分をホッ
トエアー処理することは好ましい態様である。
Means for Solving the Problems In view of the above problems, the present inventors have conducted intensive studies and as a result, the object of the present invention is to provide a polyolefin surface layer on one surface side of a substrate, One end of the polyester surface layer of the laminate film having a polyester surface layer on the surface side is folded back to the polyolefin surface layer side, the end having a surface composed of a polyolefin portion and a polyester portion, and the other surface A method of heat-sealing the container body by heat-sealing the end of the polyester surface layer on the side, wherein the surface of the polyolefin portion at the end having a surface composed of the polyolefin portion and the polyester portion is frame-treated. The surface of the polyester portion is subjected to hot air treatment, the end of the polyester surface layer on the other surface side is subjected to hot air treatment, and then both ends are treated. The surface of respectively and pressed together and found to be achieved by the method of thermal fusion bonding container body, characterized by heat sealing. In a preferred embodiment, after the polyolefin portion on the surface comprising the polyolefin portion and the polyester portion is flame-treated, the polyester portion is subjected to hot air treatment.

【0009】なお、現実的には、ポリオレフィン部分と
ポリエステル部分は隣接しており、各々の部分に当てる
フレームおよびホットエアーは、相互に多少隣接部分に
かかるが、このことは本発明の目的を阻害しない範囲で
許容されるものである。
[0009] Actually, the polyolefin portion and the polyester portion are adjacent to each other, and the frame and hot air applied to each portion are applied to the portions slightly adjacent to each other, which hinders the object of the present invention. It is acceptable within the range not to do.

【0010】以下に本発明を更に詳細に説明する。Hereinafter, the present invention will be described in more detail.

【0011】図1は本発明の熱融着方法による容器胴部
の製造の1例を示す概略工程図である。図1において、
容器内面に相当するポリエステル表面2及びその裏面に
容器外面に相当するポリオレフィン表面3とその一方の
端部4にポリエステル面2′を有する積層体フィルム1
を図1(A)に示すように端部4の裏面側のポリオレフ
ィン面3をガスバーナー5によりフレーム処理し、次い
でポリエステル面2′をホットエアー処理用ノズル6に
よりホットエアー処理する。
FIG. 1 is a schematic process diagram showing one example of the production of a container body by the heat fusion method of the present invention. In FIG.
A laminated film 1 having a polyester surface 2 corresponding to the inner surface of the container, a polyolefin surface 3 corresponding to the outer surface of the container on the back surface thereof, and a polyester surface 2 'at one end 4 thereof.
As shown in FIG. 1 (A), the polyolefin surface 3 on the back side of the end portion 4 is subjected to a frame treatment with a gas burner 5, and then the polyester surface 2 'is subjected to hot air treatment with a hot air treatment nozzle 6.

【0012】なお、ポリエステルは、水分の存在下で高
温に晒されると加水分解を起こして、ヒートシール性な
どの物性が低下するため、水分を多量に含むガス炎を使
用するフレーム処理を先に行ない、その後ホットエアー
処理を行なうことが好ましい。すなわち、ホットエアー
をポリエステルに先に当てた後、ポリオレフィンにフレ
ームを当てた場合、ポリエステルは既に十分に加熱され
ており、隣接するポリオレフィンに当てられるフレーム
の影響を受け、加水分解を起こす可能性が高いが、フレ
ーム処理を先に行なえば、ポリエステルは加熱されてお
らず、加水分解するには至らないのである。
When polyester is exposed to a high temperature in the presence of moisture, it undergoes hydrolysis and its physical properties such as heat sealability are deteriorated. Therefore, prior to the flame treatment using a gas flame containing a large amount of moisture, polyester is used. It is preferable to perform hot air treatment after that. In other words, if hot air is first applied to the polyester and then the frame is applied to the polyolefin, the polyester is already sufficiently heated and may be affected by the frame applied to the adjacent polyolefin, causing hydrolysis. Although expensive, the polyester will not be heated and will not hydrolyze if flame treatment is performed first.

【0013】一方、ポリエステル表面2の他の端部には
ホットエアー処理用ノズル6′及び6″によるホットエ
アー処理が施される。このような処理を施した後に、前
記端部4を接着に必要な所定長さ内側に折りこみ、その
外面と、図1(B)に示すようにホットエアー処理した
他の1端のポリエステル面とを互いに合わせ、圧着して
熱融着を行ない、図1(C)に示すような接着された容
器胴部が得られる。
On the other hand, the other end of the polyester surface 2 is subjected to hot air treatment by hot air treatment nozzles 6 'and 6 ". After such treatment, the end 4 is bonded. As shown in FIG. 1 (B), the inner surface is folded inward by a predetermined length, and the outer surface thereof and the other polyester surface which has been subjected to the hot air treatment are combined with each other, press-bonded and heat-fused. As a result, an adhered container body as shown in (C) is obtained.

【0014】本発明において、ポリオレフィン部分とポ
リエステル部分からなる表面のポリオレフィン部分を処
理するフレーム処理は主としてポリオレフィンを酸化し
て極性基を導入するために行なわれるが、このようなフ
レーム処理としては、好ましくは、プロパンガス等の可
燃性ガスと空気の混合ガスで燃焼させたフレームと接触
させる方法が挙げられ、接触時間は好ましくは0.001〜
1.5秒、更に好ましくは0.1〜0.6秒である。すなわち、
接触時間が0.001秒未満ではポリオレフィンの活性化が
不十分であり、ポリオレフィンとポリエステルの接着が
不十分となり、1.5秒を越える場合はポリオレフィンが
溶けて失われたり、場合によっては燃焼する。また、前
述のように、隣接するポリエステルがフレーム中に含ま
れる水分と熱の存在によって加水分解を起こし、接着性
が低下する場合がある。
In the present invention, the flame treatment for treating the polyolefin portion on the surface composed of the polyolefin portion and the polyester portion is mainly performed to oxidize the polyolefin to introduce a polar group. Is a method of contacting with a flame burned with a mixed gas of a combustible gas such as propane gas and air, and the contact time is preferably 0.001 to
It is 1.5 seconds, more preferably 0.1 to 0.6 seconds. That is,
If the contact time is less than 0.001 second, the activation of the polyolefin is insufficient, and the adhesion between the polyolefin and the polyester becomes insufficient. If the contact time exceeds 1.5 seconds, the polyolefin melts and is lost or burns in some cases. Further, as described above, the adjacent polyesters may be hydrolyzed by the presence of moisture and heat contained in the frame, and the adhesiveness may be reduced.

【0015】また、前記フレーム処理されたポリオレフ
ィン部分とポリエステル部分とからなる表面のポリエス
テル部分、及び、該ポリオレフィン部分、ポリエステル
部分と融着されることとなるポリエステル面に対して行
なわれるホットエアー処理は表面部を軟化させるために
行なわれるが、このようなホットエアー処理は、通常30
0〜1000℃の加熱空気を0.2〜5秒間ノズルを通して各々
の面に吹きつけることにより行なわれる。特に、前記ポ
リオレフィン部分とポリエステル部分とからなる表面の
ポリエステル部分を処理する場合は、通常前記フレーム
処理後、直ちに行なう必要はないが、インライン処理で
行なうことが好ましい。
Further, the hot air treatment performed on the polyester portion on the surface comprising the frame-treated polyolefin portion and the polyester portion, and on the polyester surface to be fused with the polyolefin portion and the polyester portion, This hot air treatment is usually performed to soften the surface.
This is performed by blowing heated air at 0 to 1000 ° C. through a nozzle onto each surface for 0.2 to 5 seconds. In particular, when the polyester portion on the surface comprising the polyolefin portion and the polyester portion is to be treated, it is usually not necessary to carry out the treatment immediately after the flame treatment, but it is preferable to carry out the treatment in an in-line treatment.

【0016】本発明においては、前記両面をフレーム処
理及びホットエアー処理した後、好ましくは速やかに両
面を重ね圧着して熱融着を行ない、軟化状態の両面を接
着する。この際、圧着は0.05kg/cm2以上の圧力で行な
うことが好ましい。
In the present invention, after both sides are subjected to a frame treatment and a hot air treatment, preferably, both sides are overlapped and pressed quickly and heat-fused, and the both sides in a softened state are bonded. At this time, it is preferable to perform the pressure bonding at a pressure of 0.05 kg / cm 2 or more.

【0017】本発明において、少なくともポリオレフィ
ン部分とポリエステル部分からなる表面を有する部材と
は少なくともポリオレフィンが表面に露出する部分、例
えば図4におけるY部分、及びポリエステルが表面に露
出する部分、例えば図4におけるX部分を有するもので
ある。このようなポリオレフィンとしてはポリエチレ
ン、ポリプロピレン等が用いられ、ポリエステルとして
は、容器の形成を考慮すると、ヒートシール性に優れた
ヒートシール性ポリエステル樹脂が好ましく用いられ
る。ヒートシール性ポリエステル樹脂としては、例えば
ガラス転移温度Tgが50〜150℃である低結晶性又は非結
晶性ポリエステル樹脂が挙げられる。
In the present invention, a member having a surface composed of at least a polyolefin portion and a polyester portion refers to a portion where at least the polyolefin is exposed on the surface, for example, a Y portion in FIG. 4, and a portion where the polyester is exposed on the surface, for example in FIG. It has an X portion. As such a polyolefin, polyethylene, polypropylene or the like is used. As polyester, a heat-sealable polyester resin having excellent heat-sealability is preferably used in consideration of formation of a container. Examples of the heat-sealable polyester resin include a low-crystalline or non-crystalline polyester resin having a glass transition temperature Tg of 50 to 150 ° C.

【0018】ガラス転移温度Tgが50℃以下のポリエス
テル樹脂を用いた場合、包材加工中又は保管中等に樹脂
の軟化、ベタツキによるブロッキング等が発生し作業上
問題となる場合があり、ガラス転移温度が150℃以上の
ポリエステル樹脂を用いると、ヒートシール時の製袋・
製函が困難となる場合がある。また結晶性の高いポリエ
ステル樹脂は明確な融点を有しているために低温でのヒ
ートシール性が悪く、また、脆いという欠点を有してい
る。
When a polyester resin having a glass transition temperature Tg of 50 ° C. or less is used, the softening of the resin, blocking due to stickiness, etc. may occur during processing of the packaging material or during storage, which may cause a problem in work. When using polyester resin of 150 ° C or higher,
Box making may be difficult. Further, a polyester resin having a high crystallinity has a definite melting point, so that it has poor heat-sealing properties at low temperatures and has a disadvantage of being brittle.

【0019】ポリエステル樹脂は多塩基酸と多価アルコ
ールの共重合体からなる。このような多塩基酸として
は、テレフタール酸を主成分として含むものが好まし
く、また、多価アルコールとしてはエチレングリコール
を主成分として含むものが好ましい。上記多塩基酸及び
多価アルコールはそれぞれコモノマー成分として他の多
塩基酸及び他の多価アルコールを含むことができる。
The polyester resin comprises a copolymer of a polybasic acid and a polyhydric alcohol. As such a polybasic acid, one containing terephthalic acid as a main component is preferable, and as the polyhydric alcohol, one containing ethylene glycol as a main component is preferable. The polybasic acids and polyhydric alcohols can each contain other polybasic acids and other polyhydric alcohols as comonomer components.

【0020】本発明においては、上記ヒートシール性ポ
リエステルとしては具体的には、(1)主としてテレフタ
ル酸を含む2種以上の二塩基酸と二価アルコールとの共
縮合重合体、(2)テレフタル酸と2種以上の二価アルコ
ールとの共縮合重合体、(3)ポリエチレンテレフタレー
ト又は前記(1)若しくは(2)の共縮合重合体と変性ポリオ
レフィンのポリマーアロイが挙げられる。
In the present invention, specific examples of the heat-sealable polyester include (1) a cocondensation polymer of two or more dibasic acids mainly containing terephthalic acid and a dihydric alcohol, (2) terephthalic acid. Examples thereof include a co-condensation polymer of an acid and two or more dihydric alcohols, (3) polyethylene terephthalate, or a polymer alloy of the co-condensation polymer of (1) or (2) and a modified polyolefin.

【0021】テレフタル酸とのコモノマー成分として含
むことのできる他の二塩基酸としてはイソフタール酸、
ナフタリンジカルボン酸、ジフェニルジカルボン酸、ジ
フェノキシエタンジカルボン酸、ジフェニルエーテルジ
カルボン酸、ジフェニルスルホ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ール酸、ヘキサ
ヒドロイソフタール酸等の脂環族ジカルボン酸;アジピ
ン酸、セバシン酸、アゼライン酸等の脂肪族ジカルボン
酸;p−β−ヒドロキシエトキシ安息香酸、p−オキシ
安息香酸、ε−オキシカプロン酸等のオキシ酸等が挙げ
られる。
Other dibasic acids that can be included as comonomer components with terephthalic acid include isophthalic acid,
Aromatic dicarboxylic acids such as naphthalene dicarboxylic acid, diphenyl dicarboxylic acid, diphenoxyethane dicarboxylic acid, diphenyl ether dicarboxylic acid and diphenyl sulfone dicarboxylic acid; alicyclic dicarboxylic acids such as hexahydroterephthalic acid and hexahydroisophthalic acid; adipic acid And aliphatic dicarboxylic acids such as sebacic acid and azelaic acid; and oxyacids such as p-β-hydroxyethoxybenzoic acid, p-oxybenzoic acid and ε-oxycaproic acid.

【0022】また、二価アルコールとしては、例えばエ
チレングリコール、プロピレングリコール、1,4−ブ
タンジオール、1,4−ジシクロヘキサンジメタノー
ル、トリメチレングリコール、テトラメチレングリコー
ル、ヘキサメチレングリコール、デカメチレングリコー
ル、ネオペンチレングリコール、ジエチレングリコー
ル、1,1−シクロヘキサンジメチロール、1,4−シ
クロヘキサンジメチロール、2,2−ビス(4−β−ヒ
ドロキシエトキシフェニル)プロパン、ビス−(4−β
−ヒドロキシエトキシフェニル)スルホンシクロヘキサ
ンジオール、1,4−ビス(β−ヒドロキシエトキシ)
ベンゼン、1,3−ビス(β−ヒドロキシエトキシ)ベ
ンゼン等のグリコール類等が挙げられる。
Examples of the dihydric alcohol include ethylene glycol, propylene glycol, 1,4-butanediol, 1,4-dicyclohexanedimethanol, trimethylene glycol, tetramethylene glycol, hexamethylene glycol, decamethylene glycol, and the like. Neopentylene glycol, diethylene glycol, 1,1-cyclohexane dimethylol, 1,4-cyclohexane dimethylol, 2,2-bis (4-β-hydroxyethoxyphenyl) propane, bis- (4-β
-Hydroxyethoxyphenyl) sulfonecyclohexanediol, 1,4-bis (β-hydroxyethoxy)
Glycols such as benzene and 1,3-bis (β-hydroxyethoxy) benzene are exemplified.

【0023】変性ポリオレフィンとしてはエチレンと不
飽和カルボン酸若しくはそのエステルとの共重合体、又
はアイオノマーが挙げられる。不飽和カルボン酸若しく
はそのエステルとしては、例えばアクリル酸、メタクリ
ル酸、アクリル酸メチル、メタクリル酸メチル、アクリ
ル酸エチル、メタクリル酸エチル等が挙げられる。エチ
レンと不飽和カルボン酸若しくはそのエステルとの共重
合体としては、不飽和カルボン酸の含有量が3〜20重量
%であるものが好ましく、エステルの場合はエステル成
分の含有量が1〜20重量%であるものが好ましい。
Examples of the modified polyolefin include a copolymer of ethylene and an unsaturated carboxylic acid or an ester thereof, or an ionomer. Examples of the unsaturated carboxylic acid or its ester include acrylic acid, methacrylic acid, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate and the like. As the copolymer of ethylene and an unsaturated carboxylic acid or an ester thereof, those having an unsaturated carboxylic acid content of 3 to 20% by weight are preferable. In the case of an ester, the content of the ester component is 1 to 20% by weight. % Is preferred.

【0024】本発明においては上記ポリエステル樹脂に
核剤又は種々の添加剤、例えば滑剤、アンチブロッキン
グ剤、安定剤、防曇剤、着色剤等を含有してもよい。こ
のような核剤としては2〜10μmの粒径を有するポリオ
レフィン類又は無機物の微粒子が用いられる。ポリオレ
フィン類としては例えば低密度ポリエチレン、高密度ポ
リエチレン、線状低密度ポリエチレン、ポリプロピレン
等が挙げられ、無機物としては例えばカーボンブラッ
ク、タルク、石膏、シリカ、アルミナ、炭酸カルシウ
ム、二酸化チタン、グラファイト、粉末ガラス、粉末金
属等が挙げられる。
In the present invention, the polyester resin may contain a nucleating agent or various additives such as a lubricant, an antiblocking agent, a stabilizer, an antifogging agent, a coloring agent, and the like. As such a nucleating agent, polyolefin or inorganic fine particles having a particle size of 2 to 10 μm are used. Examples of polyolefins include low-density polyethylene, high-density polyethylene, linear low-density polyethylene, and polypropylene.Examples of inorganic substances include carbon black, talc, gypsum, silica, alumina, calcium carbonate, titanium dioxide, graphite, and powdered glass. , Powdered metal and the like.

【0025】また、本発明においてポリエステル表面を
有する部材とは表面がポリエステルのみからなるものを
指し、このようなポリエステルとは前記のヒートシール
性ポリエステル樹脂と同様のものが用いられる。
In the present invention, the member having a polyester surface refers to a member whose surface is made of only polyester, and the same polyester as the heat-sealable polyester resin is used as such a polyester.

【0026】本発明における、少なくともポリオレフィ
ン部分とポリエステル部分からなる表面を有する部材と
ポリエステル表面を有する部材は、各々別個のフィルム
部材であってもよいが、好ましくは容器の製造上、基体
上の一方の面側にポリエステル表面層を有し、他方の面
側に図4に示されるようなポリエステル面とポリオレフ
ィン面からなる端部を有する表面層を有する積層体フィ
ルムが使用される。図4におけるポリエステル表面を含
む部分の折り返しの幅、すなわち、X部分の長さとして
は1〜15mmが容器製造上好ましい。上記の積層体フィル
ムとしては、例えば、ポリエステル/接着層/延伸プラ
スチック/金属箔/接着性樹脂/紙/ポリエチレン等の
層構成を有するものが用いられる。
In the present invention, the member having a surface comprising at least a polyolefin portion and a polyester portion and the member having a polyester surface may be separate film members, respectively. A laminate film having a polyester surface layer on one side and a surface layer having an end portion composed of a polyester side and a polyolefin side as shown in FIG. 4 on the other side is used. The width of the folded portion including the polyester surface in FIG. 4, that is, the length of the X portion is preferably 1 to 15 mm from the viewpoint of container production. As the above-mentioned laminated film, for example, a film having a layer structure of polyester / adhesive layer / stretched plastic / metal foil / adhesive resin / paper / polyethylene is used.

【0027】上記層構成において、ポリエステル層及び
ポリエチレン層の各々には前記のものが用いられるが、
その厚さとしてはそれぞれ5〜60μ、5〜50μが好まし
い。
In the above-mentioned layer constitution, the above-mentioned ones are used for each of the polyester layer and the polyethylene layer.
The thickness is preferably 5 to 60 μ and 5 to 50 μ, respectively.

【0028】また、接着層とは接着性樹脂、該接着性樹
脂とポリオレフィンとの積層体、または接着剤あるいは
プライマーコート剤などからなるものが用いられる。
The adhesive layer is made of an adhesive resin, a laminate of the adhesive resin and a polyolefin, or an adhesive or a primer coating agent.

【0029】前記接着性樹脂としては、例えば密度0.91
0以下のエチレン−αオレフィン共重合体、不飽和カル
ボン酸変性ポリオレフィン等が挙げられる。ポリオレフ
ィンとしては、ポリエチレン、ポリプロピレン、ポリブ
テン、エチレン−酢酸ビニル共重合体、エチレン−アク
リル酸共重合体、エチレン−メタクリル酸共重合体、エ
チレン−αオレフィン共重合体等が挙げられる。ここ
で、不飽和カルボン酸変性ポリオレフィンとはカルボン
酸基、酸無水物基及びこれらの誘導体と共重合又はグラ
フト重合させた上記ポリオレフィンを意味し、カルボン
酸基、酸無水物基及びこれらの誘導体として具体的には
メタクリル酸、マレイン酸、フマル酸、メタクリル酸無
水物、無水マレイン酸、メタクリル酸エチル、アクリル
酸グリシジル、メタクリル酸ジグリシジル等が挙げられ
る。接着剤としては、例えば1液又は2液反応型ウレタ
ン系接着剤、ポリエステル系接着剤、アクリル−ウレタ
ン系接着剤、エポキシ−ウレタン系接着剤等が挙げら
れ、プライマーコート剤としては、例えばポリエチレン
イミン、アルキルチタネート等が挙げられる。
As the adhesive resin, for example, a density of 0.91
0 or less ethylene-α-olefin copolymer, unsaturated carboxylic acid-modified polyolefin and the like. Examples of the polyolefin include polyethylene, polypropylene, polybutene, ethylene-vinyl acetate copolymer, ethylene-acrylic acid copolymer, ethylene-methacrylic acid copolymer, ethylene-α-olefin copolymer, and the like. Here, the unsaturated carboxylic acid-modified polyolefin means the above-mentioned polyolefin copolymerized or graft-polymerized with a carboxylic acid group, an acid anhydride group and a derivative thereof, and as a carboxylic acid group, an acid anhydride group and a derivative thereof. Specific examples include methacrylic acid, maleic acid, fumaric acid, methacrylic anhydride, maleic anhydride, ethyl methacrylate, glycidyl acrylate, and diglycidyl methacrylate. Examples of the adhesive include one- or two-component reactive urethane-based adhesives, polyester-based adhesives, acryl-urethane-based adhesives, and epoxy-urethane-based adhesives. Examples of the primer coating agent include polyethyleneimine. And alkyl titanates.

【0030】金属箔のクラックによる内容物の透過を防
止する等のために、延伸プラスチック層を設けることが
できる。延伸プラスチック層に含有される延伸プラスチ
ックとしては、ポリエステル樹脂又はナイロン樹脂を成
形後縦方向に4〜6倍、横方向に4〜6倍二軸延伸して
二軸延伸後熱固定した二軸延伸ポリエステル樹脂又は二
軸延伸ナイロン樹脂が好ましく用いられる。
A stretched plastic layer can be provided to prevent the contents from being transmitted due to cracks in the metal foil. As the stretched plastic contained in the stretched plastic layer, a polyester resin or a nylon resin is biaxially stretched 4 to 6 times in a longitudinal direction and 4 to 6 times in a transverse direction after molding, and then biaxially stretched and then heat-fixed. A polyester resin or a biaxially stretched nylon resin is preferably used.

【0031】また本発明に係る積層体を構成する基材に
は、容器の構造的支持体として用いられうるものならば
特に限定はないが、好ましくは基材の層構成中に紙を含
むものが好ましい。上記基材を構成する紙としては、坪
量100〜400g/m2の白板紙、ミルクカートン用原紙、耐
酸紙等が好ましく用いられる。
The substrate constituting the laminate according to the present invention is not particularly limited as long as it can be used as a structural support of the container. Preferably, the substrate contains paper in the layer constitution. Is preferred. As the paper constituting the base material, white paperboard having a basis weight of 100 to 400 g / m 2 , base paper for milk cartons, acid-resistant paper, and the like are preferably used.

【0032】上記紙上には飲料の浸透防止、外部からの
酸素の侵入を防止するガスバリヤー性付与、遮光性の付
与等のため通常金属箔が設けられており、金属箔として
は厚さ6〜200μmのアルミニウムからなるものが好まし
く用いられる。このような金属箔は例えば前述の接着性
樹脂として用いられたと同様の不飽和カルボン酸変性ポ
リオレフィン、アイオノマー樹脂等により上記紙上に設
けられる。
A metal foil is usually provided on the paper to prevent permeation of beverages, to provide gas barrier properties for preventing oxygen from entering from outside, and to provide light-shielding properties. Those made of 200 μm aluminum are preferably used. Such a metal foil is provided on the paper using, for example, the same unsaturated carboxylic acid-modified polyolefin, ionomer resin, or the like as that used as the adhesive resin.

【0033】本発明の方法を好ましく適用しうる容器と
しては、浸透性の高い液体飲料、例えば酒、ウィスキ
ー、ジュース、コーヒー、麦茶、ウーロン茶、ミネラル
ウォーター、スープ類等を内容物とする種々の形態の容
器があげられる。
The container to which the method of the present invention can be preferably applied is a liquid beverage having a high permeability, for example, alcohol, whiskey, juice, coffee, barley tea, oolong tea, mineral water, soups, etc. Container.

【0034】[0034]

【実施例】以下に実施例を挙げて、本発明を更に具体的
に説明する。
EXAMPLES The present invention will be described more specifically with reference to the following examples.

【0035】実施例1 下記層構成を有する積層体の1端部を内層の紙の層から
ポリエチレン層側を端から一定長さ除去し、図4に示す
ようにポリエステル側の残部をポリエステル層が外層と
なるように折返し幅8mmで折り返し、ポリエステル面と
ポリエチレン面からなる表面を有する積層体フィルムを
作成した。
Example 1 One end of the laminate having the following layer constitution was removed from the inner paper layer by a predetermined length from the inner side of the paper layer to the polyethylene layer side, and as shown in FIG. The laminate was folded back at a folding width of 8 mm so as to be an outer layer, to prepare a laminate film having a surface composed of a polyester surface and a polyethylene surface.

【0036】 ポリエステル (PET)/2軸延伸ポリエステル (OPET)/アルミニウム箔 (Al)/ (60μ) (12μ) (9μ) アイオノマー/ 紙 /ポリエチレン (PE) (20μ) (320g/m2) (20μ)Polyester (PET) / biaxially oriented polyester (OPET) / aluminum foil (Al) / (60μ) (12μ) (9μ) ionomer / paper / polyethylene (PE) (20μ) (320g / m 2 ) (20μ) )

【0037】但し、ポリエステルとしてはテレフタル
酸、イソフタル酸及びエチレングリコールからなるシー
ラー(Selar)PTX 207(三井・デュポンポリケミカ
ル社製)を用いた。
However, as the polyester, a sealer (Selar) PTX 207 (manufactured by Du Pont-Mitsui Polychemicals) comprising terephthalic acid, isophthalic acid and ethylene glycol was used.

【0038】上記作成したフィルムに対し、図1に示す
ようにポリエステル面とポリエチレン面とからなる表面
のポリエチレン部分を、プロパンと空気の混合ガスによ
るフレームにて0.5秒あぶり、フレーム処理した後ホッ
トエアー処理用ノズル6から400℃のホットエアーを1.5
秒間上記ポリエステル面とポリエチレン面とからなる表
面のポリエステル部分とポリエステル表面の他の端部に
吹きつけホットエアー処理を行なった。次いで、このよ
うな処理を行なった両面を直ちに0.2kg/cm2の圧力で圧
着し、熱融着を行ない、その接着強度を調べた。
As shown in FIG. 1, the polyethylene film on the surface composed of the polyester surface and the polyethylene surface was blown on the above-prepared film for 0.5 second with a flame of a mixed gas of propane and air, and after hot-air Hot air of 400 ° C from processing nozzle 6
For a second, hot air treatment was performed by spraying the polyester portion on the surface consisting of the polyester surface and the polyethylene surface and the other end of the polyester surface. Then, both surfaces treated as described above were immediately pressure-bonded at a pressure of 0.2 kg / cm 2 , heat-sealed, and the adhesive strength was examined.

【0039】結果を表1に示す。Table 1 shows the results.

【0040】尚、接着強度は以下の方法にて測定した。The adhesive strength was measured by the following method.

【0041】接着強度の測定:得られた積層体を幅15mm
の短冊状に切断し、両面の間を300mm/minの引張速度で
剥がし、その強度を測定した。
Measurement of adhesive strength: The obtained laminate was 15 mm wide.
, And peeled off between both sides at a tensile speed of 300 mm / min, and the strength was measured.

【0042】実施例2〜5 実施例1におけるポリエステルを1,4−シクロヘキサ
ンジメタノールを含むグリコール成分と二塩基酸成分と
の縮合物であるPET G 5116(イーストマン・コダッ
ク社製)にかえた以外は実施例1と同様にして実施例2
を行ない、更に実施例1におけるホットエアー処理時間
又はフレーム処理時間を第1表に示すようにかえた以外
は実施例1と同様にして実施例3〜5を各々行ない、実
施例2〜5の各々において実施例1と同様にして接着強
度を測定した。結果を表1に示す。
Examples 2 to 5 The polyester in Example 1 was replaced with PET G 5116 (manufactured by Eastman Kodak Co.), which is a condensate of a glycol component containing 1,4-cyclohexanedimethanol and a dibasic acid component. Example 2 was the same as Example 1 except for the above.
In addition, Examples 3 to 5 were performed in the same manner as in Example 1 except that the hot air processing time or the frame processing time in Example 1 was changed as shown in Table 1. In each case, the adhesive strength was measured in the same manner as in Example 1. Table 1 shows the results.

【0043】比較例1〜3 フレーム処理を行なわない以外は実施例1と同様にして
比較例1を行なった。更に比較例1においてホットエア
ー処理の時間を表1に示すようにかえた以外は比較例1
と同様にして、比較例2及び3を行なった。比較例1〜
3の各々において実施例1と同様に接着強度を測定し
た。結果を表1に示す。
Comparative Examples 1 to 3 Comparative Example 1 was performed in the same manner as in Example 1 except that the frame processing was not performed. Comparative Example 1 was the same as Comparative Example 1 except that the hot air treatment time was changed as shown in Table 1.
Comparative Examples 2 and 3 were performed in the same manner as described above. Comparative Examples 1 to
In each of the three samples, the adhesive strength was measured in the same manner as in Example 1. Table 1 shows the results.

【0044】比較例4〜7 ホットエアー処理を行なわない以外は、実施例1と同様
にして比較例4を行なった。更に、比較例4においてフ
レーム処理時間を表1に示すようにかえた以外は比較例
4と同様にして比較例5〜7を行なった。比較例4〜7
の各々において実施例1と同様に接着強度を測定した。
結果を表1に示す。
Comparative Examples 4 to 7 Comparative Example 4 was performed in the same manner as in Example 1 except that the hot air treatment was not performed. Further, Comparative Examples 5 to 7 were performed in the same manner as in Comparative Example 4 except that the frame processing time in Comparative Example 4 was changed as shown in Table 1. Comparative Examples 4 to 7
In each case, the adhesive strength was measured in the same manner as in Example 1.
Table 1 shows the results.

【0045】[0045]

【表1】 表1より明らかなように、ホットエアー処理のみを行な
った比較例1〜3ではポリオレフィン/ポリエステル間
の接着が不十分であり、フレーム処理のみを行なった比
較例4〜7ではポリエステル同志の接着が不十分又は不
可能であるが、実施例1〜5におけるように、フレーム
処理およびホットエアー処理をそれぞれ所定の部位に対
して行なうことにより、ポリオレフィン/ポリエステル
間及びポリエステル同志のいずれにおいても良好な接着
が行なわれた。
[Table 1] As is clear from Table 1, in Comparative Examples 1 to 3 in which only the hot air treatment was performed, the adhesion between the polyolefin and the polyester was insufficient, and in Comparative Examples 4 to 7 in which only the frame treatment was performed, the adhesion between the polyesters was poor. Insufficient or impossible, but as in Examples 1-5, good adhesion both at polyolefin / polyester and between polyesters by applying flame treatment and hot air treatment to predetermined sites, respectively. Was done.

【0046】[0046]

【発明の効果】以上詳細に説明したように、本発明の熱
融着方法により、ポリオレフィン部分とポリエステル部
分とからなる表面とポリエステル表面とを同時に、かつ
インラインで良好な接着強度をもって熱融着することが
できる。
As described above in detail, according to the heat-sealing method of the present invention, the surface consisting of the polyolefin portion and the polyester portion and the polyester surface are heat-sealed simultaneously and in-line with good adhesive strength. be able to.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の熱融着方法の1実施例を示す概略工程
図である。
FIG. 1 is a schematic process diagram showing one embodiment of a heat fusion method of the present invention.

【図2】図1の(A)工程におけるその進行方向側から
見た断面図である。
FIG. 2 is a cross-sectional view of the step (A) in FIG. 1 as viewed from the direction of travel.

【図3】本発明の方法により作成される容器の1例の胴
部を示す概略斜視図である。
FIG. 3 is a schematic perspective view showing a body of an example of a container made by the method of the present invention.

【図4】図3のA部の拡大断面図であり、本発明の方法
により接着される部分の1例を示す。
FIG. 4 is an enlarged cross-sectional view of a portion A in FIG. 3, showing an example of a portion bonded by the method of the present invention.

【符号の説明】[Explanation of symbols]

1 積層体フィルム 2,2′ ポリエステル面 3 ポリオレフィン面 4 端部 5 ガスバーナー 6,6′,6″ ホットエアー処理用ノズル 7 ポリエステル層 8 接着層 9 二軸延伸ポリエステル層 10 紙 11 アルミニウム箔 12 ポリオレフィン層 A 端部熱融着部分 Reference Signs List 1 laminated film 2, 2 'polyester surface 3 polyolefin surface 4 end 5 gas burner 6, 6', 6 "nozzle for hot air treatment 7 polyester layer 8 adhesive layer 9 biaxially oriented polyester layer 10 paper 11 aluminum foil 12 polyolefin Layer A Edge heat-sealed part

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭49−99371(JP,A) 特開 昭57−135141(JP,A) 特開 平2−80235(JP,A) 米国特許4698246(US,A) ────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-49-99371 (JP, A) JP-A-57-135141 (JP, A) JP-A-2-80235 (JP, A) US Pat. , A)

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 基体上の一方の面側にポリオレフィン表
面層を有し、他方の面側にポリエステル表面層を有する
積層体フィルムの前記ポリエステル表面層の一方の端部
を前記ポリオレフィン表面層側に折り返して形成された
ポリオレフィン部分とポリエステル部分からなる表面を
有する端部と、他方の面側のポリエステル表面層の端部
とを熱融着する容器胴部の熱融着方法であり、前記ポリ
オレフィン部分と前記ポリエステル部分からなる表面を
有する端部の前記ポリオレフィン部分の表面をフレーム
処理すると共に前記ポリエステル部分の表面をホットエ
アー処理し、他方の面側のポリエステル表面層の端部を
ホットエアー処理し、次いで両端部のそれぞれの表面を
互いに圧着して熱融着することを特徴とする容器胴部の
熱融着方法。
1. One end of the polyester surface layer of a laminate film having a polyolefin surface layer on one side of the substrate and a polyester surface layer on the other side is placed on the polyolefin surface layer side. A method for heat-sealing a container body for heat-sealing an end having a surface composed of a polyolefin portion and a polyester portion formed by folding, and an end of a polyester surface layer on the other surface side, wherein the polyolefin portion is And the surface of the polyolefin portion of the end having the surface consisting of the polyester portion and the surface of the polyester portion and the surface of the polyester portion is subjected to hot air treatment, the other surface side of the polyester surface layer is subjected to hot air treatment, Then, the respective surfaces of both ends are pressure-bonded to each other and heat-sealed.
【請求項2】 前記ポリオレフィン部分及びポリエステ
ル部分からなる表面のポリオレフィン部分をフレーム処
理した後にポリエステル部分をホットエアー処理するこ
とを特徴とする請求項1記載の容器胴部の熱融着方法。
2. The method according to claim 1, wherein the polyester portion is subjected to hot air treatment after the polyolefin portion on the surface comprising the polyolefin portion and the polyester portion is subjected to a flame treatment.
JP3216037A 1991-08-01 1991-08-01 Heat fusion method of container body Expired - Fee Related JP2661427B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP3216037A JP2661427B2 (en) 1991-08-01 1991-08-01 Heat fusion method of container body
DE69207843T DE69207843T2 (en) 1991-08-01 1992-07-30 Hot glue process
EP92112987A EP0529336B1 (en) 1991-08-01 1992-07-30 Method of thermal fusion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3216037A JP2661427B2 (en) 1991-08-01 1991-08-01 Heat fusion method of container body

Publications (2)

Publication Number Publication Date
JPH0531832A JPH0531832A (en) 1993-02-09
JP2661427B2 true JP2661427B2 (en) 1997-10-08

Family

ID=16682298

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3216037A Expired - Fee Related JP2661427B2 (en) 1991-08-01 1991-08-01 Heat fusion method of container body

Country Status (1)

Country Link
JP (1) JP2661427B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002337840A (en) * 2001-05-10 2002-11-27 Jujo Central Co Ltd Packaging container
TR201910731T4 (en) * 2013-04-10 2019-08-21 Tetra Laval Holdings & Finance The method and device that realizes the method for processing packaging laminate

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4698246A (en) 1986-03-05 1987-10-06 International Paper Company Novel laminates for paperboard cartons and a process of forming said laminates

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4999371A (en) * 1973-01-22 1974-09-19
JPS57135141A (en) * 1981-02-16 1982-08-20 Dainippon Printing Co Ltd Manufacture of packing case
JP2619344B2 (en) * 1988-09-16 1997-06-11 アロン化成株式会社 Laminated structure

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4698246A (en) 1986-03-05 1987-10-06 International Paper Company Novel laminates for paperboard cartons and a process of forming said laminates

Also Published As

Publication number Publication date
JPH0531832A (en) 1993-02-09

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