JPS6340747B2 - - Google Patents

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Publication number
JPS6340747B2
JPS6340747B2 JP6340881A JP6340881A JPS6340747B2 JP S6340747 B2 JPS6340747 B2 JP S6340747B2 JP 6340881 A JP6340881 A JP 6340881A JP 6340881 A JP6340881 A JP 6340881A JP S6340747 B2 JPS6340747 B2 JP S6340747B2
Authority
JP
Japan
Prior art keywords
polyester
container
label
bottle
thin film
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
Application number
JP6340881A
Other languages
Japanese (ja)
Other versions
JPS57194950A (en
Inventor
Tooru Matsubayashi
Tooru Utsunomya
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.)
Teijin Ltd
Original Assignee
Teijin 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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP6340881A priority Critical patent/JPS57194950A/en
Publication of JPS57194950A publication Critical patent/JPS57194950A/en
Publication of JPS6340747B2 publication Critical patent/JPS6340747B2/ja
Granted legal-status Critical Current

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Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/62Plastics recycling; Rubber recycling

Landscapes

  • Lining Or Joining Of Plastics Or The Like (AREA)
  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
  • Details Of Rigid Or Semi-Rigid Containers (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

本発明はポリ゚ステル容噚に関する。曎に詳し
くは、本発明は䜿甚枈の空容噚を有効再利甚する
際に、ポリ゚ステル以倖の成分を分離する煩雑な
操䜜を省略しうるポリ゚ステル容噚に関するもの
である。 近幎、ポリ゚チレンテレフタレヌトを代衚ずす
る熱可塑性ポリ゚ステルは、その機械的特性、ガ
スバリア性、耐薬品性、保銙性、透明性、衛生性
等が優れおいるこずから各皮の包装甚容噚ずしお
䜿甚されおいる。 この熱可塑性ポリ゚ステルよりなる容噚は、通
垞容噚本䜓はポリ゚ステルより構成されるが、容
噚党䜓ずしおは他の郚分をポリ゚ステル以倖の成
分で構成した圢態で䜿甚されおいる。䟋えば栓は
ポリ゚チレン補たたは金属補のもの、ラベルは玙
補のもの、曎に炭酞飲料等の加圧容噚における脚
台はポリ゚チレン補のものが甚いられおいる。 かかる容噚は、通垞䜿い捚お容噚ずしお䜿甚さ
れおいるが、省資源或いは環境保護の点から容噚
を回収しお有効に再利甚する事が望たれおいる。 かかる再利甚方法ずしおは、ポリマヌずしお再
び成圢甚材料ずしお䜿甚する方法或いは、ポリ゚
ステルの玠原料であるテレフタル酞或いはその゚
ステル圢成性誘導䜓及び゚チレングリコヌルに分
解し、粟補したのち、ポリマヌ原料ずしお再䜿甚
する方法が知られおいる。しかし、いずれの再利
甚法においおも、ポリ゚ステル以倖の成分よりな
る構成郚分、䟋えばアルミニりム補栓などの金属
材料、ポリ゚チレン補栓、脚台、玙ラベル等はあ
らかじめ分離する必芁がある。 これらのポリ゚ステル以倖の成分を分離する方
法ずしおは、䟋えば鉄等の磁性䜓を探知機により
陀倖する方法、ラベルに䜿甚される玙等の軜量物
を圧空により分離する方法、キダツプに䜿甚され
るアルミニりム等の非鉄金属を枊電流により分離
する方法、脚台等に䜿甚されるポリ゚チレン或い
はガラス等の重量異物を比重差を利甚しお氎溶液
䞭で分離する方法等が考えられる。 本発明者はかかる煩雑な分離操䜜を行うこずな
く、有効に再生利甚し埗る容噚に぀いお鋭意怜蚎
の結果、ポリ゚ステルを特殊な成圢技術により加
工した構成郚分をポリ゚ステル容噚に䜿甚するな
らば目的ずする容噚を埗るこずのできるこずを芋
い出し、本発明に到達した。 すなわち、本発明は  容噚本䜓が゚チレンテレフタレヌトを䞻たる
繰り返し単䜍ずするポリ゚ステルよりなり、
該容噚の栓、蓋、把持甚把手及び脚台よりなる
構成郚分の材質が金属材料を陀き゚チレンテレ
フタレヌトを䞻たる繰り返し単䜍ずするポリ゚
ステルよりなり、か぀該容噚が゚チレンテレ
フタレヌトを䞻たる繰り返し単䜍ずするポリ゚
ステルよりなる収瞮された筒状薄葉䜓からな
るラベルを付されおなるポリ゚ステル容噚、䞊
びに  ゚チレンテレフタレヌトを䞻たる繰り返し単
䜍ずするポリ゚ステルよりなる容噚本䜓の胎
郚に、゚チレンテレフタレヌトを䞻たる繰り返
し単䜍ずするポリ゚ステルのラベルを装着す
るに際し、その密床が1.38cm3以䞋でありか
぀面配向床が0.02以䞊の筒状薄葉䜓を前蚘胎郚
の倖偎にかぶせ、該薄葉䜓を構成する該ポリ゚
ステルのガラス転移枩床以䞊の枩床で該薄葉
䜓を収瞮させおラベル化するこずを特城ずする
ポリ゚ステル容噚の補造法 である。 本発明においお容噚本䜓を構成するポリ゚ステ
ルは、゚チレンテレフタレヌトを䞻たる繰り返
し単䜍ずする熱可塑性ポリ゚ステルであり、ポリ
゚チレンテレフタレヌトのホモポリマヌを䞻たる
察象ずするが、テレフタル酞成分の䞀郚を䟋えば
む゜フタル酞、ナフタリンゞカルボン酞、ゞプ
ニルゞカルボン酞、ゞプノキシ゚タンゞカルボ
ン酞、ゞプニル゚ヌテルゞカルボン酞、ゞプ
ニルスルホンゞカルボン酞等の劂き芳銙族ゞカル
ボン酞ヘキサヒドロテレフタル酞、ヘキサヒド
ロむ゜フタル酞等の劂き脂環族ゞカルボン酞ア
ゞピン酞、セバチン酞、アれラむン酞等の劂き脂
肪族ゞカルボン酞−β−ヒドロキシ゚トキシ
安息銙酞、ε−オキシカプロン酞等の劂きオキシ
酞等の他の二官胜性カルボン酞の䞀皮以䞊で、及
び又ぱチレングリコヌル成分の䞀郚を䟋えば
トリメチレングリコヌル、テトラメチレングリコ
ヌル、ヘキサメチレングリコヌル、デカメチレン
グリコヌル、ネオペンチレングリコヌル、ゞ゚チ
レングリコヌル、−シクロヘキサンゞメチ
ロヌル、−シクロヘキサンゞメチロヌル、
−ビス4′−β−ヒドロキシ゚トキシプ
ニルプロパン、ビス4′−β−ヒドロキシ゚ト
キシプニルスルホン酞等の他のグリコヌル及
びこれらの機胜的誘導䜓の倚官胜化合物の䞀皮以
䞊で眮換しお共重合せしめたコポリマヌであ぀お
もよい。コポリ゚ステル䞭の共重合成分の割合は
10モル皋床以䞋が奜たしい。 本発明においお容噚の構成郚分、すなわち蓋、
栓、把持甚把手及び脚台ぱチレンテレフタレヌ
トを䞻たる繰り返し単䜍ずするポリ゚ステルを
構成成分ずするものである。たた容噚本䜓の胎郚
に付するラベルずなる薄葉䜓も゚チレンテレフタ
レヌトを䞻たる繰り返し単䜍ずするポリ゚ステル
により構成される。ここにポリ゚ステル及び
ポリ゚ステルは、同䞀か又は重合床や倉性床の
異なる、ポリ゚チレンテレフタレヌトのホモポリ
マヌ䞻たる察象又はテレフタル酞成分の䞀郚
及び又ぱチレングリコヌル成分の䞀郚を共重
合成分で眮換しお共重合せしめたコポリマヌであ
぀おもよい。かかる共重合成分は、前蚘ポリ゚ス
テルの共重合成分ずしお䟋瀺したものを挙げる
こずができる。このコポリマヌ䞭の共重合成分の
割合は構成郚分の皮類によ぀お倉り、栓及び把持
甚把手を構成するものは30モル皋床以䞋、蓋及
びラベルを構成するものは50モル皋床以䞋が奜
たしい。 本発明のポリ゚ステル容噚を炭酞飲料等の加圧
容噚ずしお甚いる堎合、通垞該ポリ゚ステル容噚
に脚台を装眮するが、この脚台及び該脚台を装着
するのに䜿甚するこずのある接着剀も前蚘ポリ゚
ステル乃至及びポリ゚ステル系接着剀よりな
るこずが奜たしい。脚台を構成するポリ゚ステル
ずしおコポリマヌを甚いるずきには共重合成分
が30モル皋床以䞋のコポリ゚チレンテレフタレ
ヌトであるこずが奜たしい。 本発明で云う容噚本䜓は䟋えば射出吹蟌成圢、
抌出吹蟌成圢によるボトル状容噚、或いは熱成圢
法によるカツプ状容噚等、液䜓或いは固䜓状内容
物を充填し埗る郚分であり、特に軞的に配向さ
れた郚分を有するボトル状容噚いわゆる軞延
䌞吹蟌成圢法により埗られる容噚が、食品或い
は飲料甚容噚ずしお倚量に䜿甚されるため、䞻な
察象ずなる。 曎にポリ゚ステル容噚における構成郚分は䟋え
ば以䞋に述べるものである。 ラベルポリ゚ステルをパむプ状に抌し出し成
圢し、実質的に分子配向が生じる枩床範囲でよ
こ方向に延䌞せしめた筒状の薄葉䜓を容噚にか
ぶせお熱収瞮により容噚に装着せしめたもの。 脚台射出成圢により成圢したもの、或いはポリ
゚ステルシヌトを熱成圢により成圢したもの
を、ボトル底郚に接着剀により、又は熱接着に
より接着せしめたもの、或いは脚台を熱倉圢に
よりボトルに接合せしめたもの。 栓、把手射出成圢により成圢したもの。 ラツプむンフレヌシペン等により成圢した筒状
フむルムの䞡端をヒヌトシヌルしたもの。 かかる容噚構成成分はボトル容噚の堎合におい
おは䟋えば添付図に瀺すように取付けられる。第
図及び第図はボトルの郚分偎面図及び郚分断
面図である。第図においおはボトル本䜓、
はラベル、は自立甚の脚台、は栓、は栓の
内蓋、は脚台ずボトルずの接着剀局をそれぞれ
瀺す。たた第図においおは把手を瀺す。第
図及び第図はボトル底郚の拡倧郚分偎面図及び
郚分断面図である。はボトル本䜓に付けた凹
み、は脚台の䞊端郚、はボトル底郚、
は接着剀局を瀺す。 本発明においおラベル付きポリ゚ステル容噚を
補造する堎合、ポリ゚ステル補筒状薄葉䜓を熱可
塑性ポリ゚ステル容噚本䜓にかぶせた埌、熱収瞮
により容噚本䜓に密着させおラベル化するのが奜
たしい。この堎合薄葉䜓の密床は1.38cm3以䞋
であるこずが奜たしく、密床が1.38cm3よりも
倧きいず、均䞀収瞮が困難ずなり奜たしくない。
たた薄葉䜓の面配向床は0.02以䞊であるこずが奜
たしく、特に筒の軞方向の面配向床△ny−
よりも暪方向の面配向床△nx−が倧きい
事が奜たしい。最も奜たしくは、△nx−≧
0.05、△nx−△ny−≧の範囲であり、
ラベルの瞊方向の寞法粟床が良奜ずなりか぀密着
性が良奜ずなる。薄葉䜓を収瞮させる際の枩床は
薄葉䜓を構成するポリ゚ステルのガラス転䜍枩
床Tg以䞊であるこずが奜たしく、この枩床
がTgよりも䜎いずラベルの密着性が悪くなる。
収瞮枩床の䞊限は熱可塑性ポリ゚ステル容噚本䜓
が実質的に倉圢しない枩床ずするのが奜たしい。 ラベルの厚みは容噚本䜓の厚みの1/10以䞋が奜
たしく、䟋えば50Ό以䞋である。ラベルの厚みが
厚過ぎるず、ラベルを熱収瞮させる際に容噚本䜓
も収瞮倉圢する堎合もあり、奜たしくない。 たた、脚台をボトル底郚に接合させる方法ずし
おは䟋えば第図に瀺す劂く、ボトル本䜓にで
瀺す劂き凹みを付けお眮き、脚台の䞊端を熱倉
圢によりの郚分に抌し蟌む方法或いは第図に
瀺す劂く、脚台ずボトルずは熱接着により接合す
る方法を甚いるず良い。 以䞋、実斜䟋により本発明を詳述する。なお䞻
な特性倀の枬定条件は次の通りである。 ガラス転䜍枩床Tg 290℃で溶融したのち℃たで急冷したサンプ
ルを瀺差熱量蚈パヌキン゚ルマヌ瀟補DSC−
型を䜿甚により10℃minの昇枩速床で枬
定。 極限粘床〔IV〕 −クロロプノヌルを溶媒ずしお35℃で枬
定。 配向床△ アツベ屈折率蚈に偏光板を装眮し、容噚から切
り取぀たサンプルの厚さ方向及び平面方向の屈折
率を枩床25℃でナトリりムの線を甚いお枬定し
た䞡者の倀の差を蚈算により求めた。 軟化点Tsp ポリマヌチツプ圢状玄mm×mm×mmを
140℃で時間凊理したものを軟化点詊隓機内に
入れ、断面積mm2の先端をも぀針にKgの荷重を
加え、50℃hrの昇枩速床で昇枩させお針入深さ
がmmに達した枩床を枬定し、その倀を軟化点ず
した。 密床ρ 四塩化炭玠ず−ヘプタンより䜜成した密床募
配管にお25℃にお枬定。 実斜䟋及び比范䟋 IV0.74、Tg77℃、Tsp259℃であるポリ
゚チレンテレフタレヌトを陀湿也燥噚にお160℃
で時間也燥し、チツプ䞭の氎分が0.01以䞋の
也チツプを埗た。この也チツプを甚いお、オン
スの射出成圢機名機補䜜所補−100型機及
びホツトランナヌ匏個取り金型により、盎胎郚
倖埄25mm、長さ175mm、肉厚3.5mm及び重量50grの
有底プリフオヌムを成圢した。成圢条件はシリン
ダヌ蚭定枩床265〜270℃ノズル郚での暹脂枩床
285℃、射出圧力500〜700Kgcm3、成圢サむクル
35秒、金型冷华氎枩床10〜20℃、射出成圢機シリ
ンダヌ内での暹脂の滞留時間玄分ずした。埗ら
れたプリフオヌムは透明性の良奜な実質的に非晶
のものであ぀た。このプリフオヌムを甚いお、延
䌞吹蟌成圢機シンシナテむミラクロン瀟補
RHB−型機により、胎郚の盎埄80mm、高さ
260mmの䞞底匏1lit炭酞飲料甚ボトル状の圢状を
有するボトルを成圢した。この時のブロ成圢条件
は次の通りであ぀た。 予熱完了時のプリフオヌム倖衚面枩床100〜130
℃ ブロヌ圧力次圧 Kgcm2 次圧 15〜18Kgcm2 かくしお埗られたボトルの物性は䞋蚘の通りで
あ぀た。 胎郚肉厚0.35〜0.45mm 透明性良奜 胎郚光線透過率90 萜䞋匷床ボトルにH2Oを充填し、打栓したの
ち、底郚を䞋にしおの高さよりコンクリヌ
ト床面に萜䞋させお砎裂する事が無か぀た。 内圧匷床ボトル内郚に埐々に氎圧を加えた結
果、圧力16Kgcm2で砎裂した。 ラベル極限粘床0.65、軟化点256℃、ガラス転
䜍枩床78℃のポリ゚チレンテレフタレヌト粒子
を、熱颚也燥噚䞭で160℃、時間也燥しお、
粒子䞭の氎分率を0.01重量ずしたのち、抌出
機にお倖埄11mm、肉厚玄mmのパむプ状成圢品
は270℃にお抌し出し、盎ちに氎冷しお透明性
の良奜なパむプを成圢した。次いでこのパむプ
を90℃の熱氎䞭に浞挬し、軞方向に玄1.5倍延
䌞するず共にバむプ内に吹蟌んだ加圧空気によ
り暪方向に玄倍膚脹させ、盎ちに冷华する事
により、盎埄玄85mm、肉厚玄0.08mmの筒状肉薄
フむルムを埗た。 該フむルム衚面に印刷を斜したのち、巟玄80
mmに切断し、胎郚の倖埄82mmの前蚘方法で埗た
ボトルの胎郚倖偎に該円筒状肉薄フむルムを芆
せたのち、玄100℃の熱颚を吹き付け円筒状肉
薄フむルムを収瞮せしめおボトル胎郚にラベル
状に装着せしめた。 䞊蚘同様にしお筒状肉薄フむルムの成圢条件及
び収瞮条件を皮々倉えお実斜した結果を衚−に
瀺す。
The present invention relates to polyester containers. More specifically, the present invention relates to a polyester container that can omit the complicated operation of separating components other than polyester when effectively reusing used empty containers. In recent years, thermoplastic polyesters such as polyethylene terephthalate have been used for various packaging containers due to their excellent mechanical properties, gas barrier properties, chemical resistance, fragrance retention, transparency, hygiene, etc. There is. Containers made of thermoplastic polyester usually have a main body made of polyester, but other parts of the container as a whole are made of components other than polyester. For example, stoppers are made of polyethylene or metal, labels are made of paper, and legs of pressurized containers for carbonated drinks and the like are made of polyethylene. Such containers are normally used as disposable containers, but from the standpoint of resource conservation and environmental protection, it is desired that the containers be recovered and reused effectively. Such recycling methods include reusing it as a polymer as a molding material, or decomposing it into terephthalic acid, which is the raw material for polyester, or its ester-forming derivative and ethylene glycol, purifying it, and then reusing it as a polymer raw material. method is known. However, in any of the recycling methods, it is necessary to separate components made of components other than polyester, such as metal materials such as aluminum stoppers, polyethylene stoppers, footrests, paper labels, etc. Methods for separating components other than polyester include, for example, using a detector to exclude magnetic substances such as iron, separating lightweight materials such as paper used for labels using compressed air, and separating aluminum used for caps. Possible methods include separating non-ferrous metals such as metals using eddy current, and separating heavy foreign substances such as polyethylene or glass used in footrests in an aqueous solution by utilizing the difference in specific gravity. As a result of intensive studies on containers that can be effectively recycled without performing such complicated separation operations, the inventor of the present invention found that if polyester components processed using a special molding technique are used in polyester containers, the desired container can be used. The inventors have discovered that it is possible to obtain the following, and have arrived at the present invention. That is, the present invention has the following features: 1. The container body is made of polyester A having ethylene terephthalate as the main repeating unit,
The material of the component parts of the container, including the stopper, lid, gripping handle, and footrest, excluding metal materials, is made of polyester B whose main repeating unit is ethylene terephthalate, and the container is made of polyester B whose main repeating unit is ethylene terephthalate. A polyester container with a label made of a shrunken cylindrical thin film made of C; When attaching a label made of polyester C, a cylindrical thin film body having a density of 1.38 g/cm 3 or less and a degree of plane orientation of 0.02 or more is placed over the outside of the body, and the polyester C constituting the thin film body is covered. This is a method for producing a polyester container, characterized by forming a label by shrinking the thin film at a temperature equal to or higher than the glass transition temperature of the polyester container. In the present invention, the polyester A constituting the container body is a thermoplastic polyester having ethylene terephthalate as a main repeating unit, and is mainly intended for use as a homopolymer of polyethylene terephthalate. Aromatic dicarboxylic acids such as dicarboxylic acid, diphenyl dicarboxylic acid, diphenoxyethane dicarboxylic acid, diphenyl ether dicarboxylic acid, diphenylsulfone dicarboxylic acid, etc.; Alicyclic dicarboxylic acids such as hexahydroterephthalic acid, hexahydroisophthalic acid, etc. Acids; aliphatic dicarboxylic acids such as adipic acid, sebacic acid, azelaic acid, etc.; other difunctional carboxylic acids such as oxyacids such as P-β-hydroxyethoxybenzoic acid, ε-oxycaproic acid, etc.; , and/or a part of the ethylene glycol component, such as trimethylene glycol, tetramethylene glycol, hexamethylene glycol, decamethylene glycol, neopentylene glycol, diethylene glycol, 1,1-cyclohexane dimethylol, 1,4-cyclohexane dimethylol ,
One or more polyfunctional compounds of other glycols and functional derivatives thereof such as 2,2-bis(4'-β-hydroxyethoxyphenyl)propane and bis(4'-β-hydroxyethoxyphenyl)sulfonic acid It may also be a copolymer substituted with and copolymerized. The proportion of copolymerized components in the copolyester is
It is preferably about 10 mol% or less. In the present invention, the component parts of the container, namely the lid,
The stopper, the gripping handle, and the base are composed of polyester B having ethylene terephthalate as a main repeating unit. Further, the thin film material serving as the label attached to the body of the container body is also composed of polyester C having ethylene terephthalate as a main repeating unit. Here, polyester B and polyester C are homopolymers of polyethylene terephthalate (main target), which are the same or have different degrees of polymerization or modification, or copolymerized components of a part of the terephthalic acid component and/or a part of the ethylene glycol component. It may also be a substituted copolymer. Such copolymerization components include those exemplified as the copolymerization component of polyester A above. The proportion of copolymerized components in this copolymer varies depending on the type of component, and is preferably about 30 mol% or less for the stopper and gripping handle, and about 50 mol% or less for the lid and label. . When the polyester container of the present invention is used as a pressurized container for carbonated beverages, etc., a leg base is usually attached to the polyester container, and the leg base and the adhesive that may be used to attach the leg base are also as described above. It is preferably made of polyesters A to C and a polyester adhesive. When a copolymer is used as the polyester B constituting the footrest, it is preferably copolyethylene terephthalate with a copolymerization component of about 30 mol% or less. The container body referred to in the present invention may be formed by injection blow molding, for example.
A bottle-shaped container made by extrusion blow molding or a cup-shaped container made by thermoforming, which can be filled with a liquid or solid content, and especially a bottle-shaped container having a biaxially oriented portion (so-called biaxial Containers obtained by stretch blow molding are the main target because they are used in large quantities as food or beverage containers. Furthermore, the constituent parts of the polyester container are, for example, those described below. Label: A cylindrical thin film made by extruding polyester C into a pipe shape, stretched in the horizontal direction at a temperature range that substantially causes molecular orientation, is placed over the container, and attached to the container by heat shrinkage. Leg: molded by injection molding, or thermoformed from a polyester sheet and bonded to the bottom of the bottle with adhesive or thermal bonding, or the leg is bonded to the bottle by thermal deformation. thing. Stoppers and handles: Molded by injection molding. Wrap: A cylindrical film formed by inflation, etc., with both ends heat-sealed. In the case of a bottle container, such container components are mounted, for example, as shown in the accompanying drawings. 1 and 2 are a partial side view and a partial sectional view of the bottle. In Figure 1, 1 is the bottle body, 2
3 is a label, 3 is a stand for self-supporting, 4 is a stopper, 5 is an inner lid of the stopper, and 6 is an adhesive layer between the stand and the bottle. Further, in FIG. 2, 7 indicates a handle. Third
FIG. 4 is an enlarged partial side view and partial cross-sectional view of the bottom of the bottle. 8 is a recess made in the bottle body 1, 9 is the upper end of the leg stand 6, 10 is the bottom of the bottle, 1
1 indicates an adhesive layer. When manufacturing a polyester container with a label in the present invention, it is preferable to cover the thermoplastic polyester container body with a cylindrical thin polyester material and then heat shrink the polyester container so that the polyester container is brought into close contact with the container body to form a label. In this case, the density of the thin film is preferably 1.38 g/cm 3 or less; if the density is greater than 1.38 g/cm 3 , uniform shrinkage becomes difficult, which is not preferred.
In addition, it is preferable that the degree of plane orientation of the thin film is 0.02 or more, especially the degree of plane orientation in the axial direction of the cylinder (△ny−z).
It is preferable that the degree of plane orientation (△nx−z) in the lateral direction is larger than that. Most preferably, △nx−z≧
0.05, in the range of △nx−z/△ny−z≧2,
The dimensional accuracy of the label in the vertical direction becomes good and the adhesion becomes good. The temperature at which the thin film is shrunk is preferably higher than the glass transition temperature (Tg) of polyester C constituting the thin film; if this temperature is lower than Tg, the adhesion of the label will deteriorate.
The upper limit of the shrinkage temperature is preferably set to a temperature at which the thermoplastic polyester container body is not substantially deformed. The thickness of the label is preferably 1/10 or less of the thickness of the container body, for example, 50ÎŒ or less. If the label is too thick, the container body may also shrink and deform when the label is heat-shrinked, which is not preferable. Further, as a method of joining the leg base to the bottom of the bottle, for example, as shown in FIG. 3, a method is employed in which a recess as shown by 8 is made in the bottle body and the upper end 9 of the leg base is pushed into the part 8 by thermal deformation. As shown in FIG. 4, it is preferable to use a method of bonding the foot stand and the bottle by thermal bonding. Hereinafter, the present invention will be explained in detail with reference to Examples. The measurement conditions for the main characteristic values are as follows. Glass transition temperature (Tg): A sample melted at 290℃ and then rapidly cooled to 0℃ was measured using a differential calorimeter (DSC- manufactured by PerkinElmer).
1) at a heating rate of 10℃/min. Intrinsic viscosity [IV]: Measured at 35°C using o-chlorophenol as a solvent. Orientation degree (△n): Measure the refractive index in the thickness direction and in the plane direction of a sample cut from a container using a sodium D line at a temperature of 25°C using an Atsube refractometer equipped with a polarizing plate. The difference was determined by calculation. Softening point (Tsp): Polymer chips (shape approx. 4mm x 4mm x 2mm)
The material treated at 140℃ for 1 hour was placed in a softening point tester, a load of 1kg was applied to a needle with a tip with a cross-sectional area of 1mm2 , and the temperature was raised at a rate of 50℃/hr to determine the penetration depth. The temperature at which the temperature reached 1 mm was measured, and that value was taken as the softening point. Density (ρ): Measured at 25°C using a density gradient tube made from carbon tetrachloride and n-heptane. Examples and Comparative Examples Polyethylene terephthalate with IV = 0.74, Tg = 77°C, and Tsp = 259°C was heated to 160°C in a dehumidifying dryer.
The chips were dried for 4 hours to obtain dry chips with a moisture content of 0.01% or less. Using this dry chip, an 8-ounce injection molding machine (M-100 model manufactured by Meiki Manufacturing Co., Ltd.) and a hot runner type two-cavity mold were used to mold the straight body with an outer diameter of 25 mm, a length of 175 mm, and a wall thickness of 3.5 mm. A bottomed preform weighing 50 gr was molded. The molding conditions are cylinder set temperature 265-270℃ (resin temperature at nozzle part)
285℃), injection pressure 500-700Kg/cm 3 , molding cycle
The mold cooling water temperature was 10 to 20°C, and the residence time of the resin in the injection molding machine cylinder was about 2 minutes. The obtained preform was substantially amorphous with good transparency. Using this preform, a stretch blow molding machine (manufactured by Cincinnati Milacron Co., Ltd.)
RHB-L type machine), body diameter 80mm, height
A 260 mm round-bottom 1 liter bottle shaped like a carbonated beverage bottle was molded. The blow molding conditions at this time were as follows. Preform outer surface temperature upon completion of preheating: 100 to 130
C. Blow pressure: Primary pressure: 6 Kg/cm 2 G Secondary pressure: 15 to 18 Kg/cm 2 G The physical properties of the bottle thus obtained were as follows. Body wall thickness: 0.35 to 0.45mm Transparency: Good Body light transmittance: 90% Drop strength: After filling a bottle with H 2 O and capping it, drop it from a height of 2m on a concrete floor with the bottom facing down. It did not explode when dropped. Internal pressure strength: As a result of gradually applying water pressure inside the bottle, the bottle burst at a pressure of 16 kg/cm 2 G. Label: Polyethylene terephthalate particles with an intrinsic viscosity of 0.65, a softening point of 256°C, and a glass transition temperature of 78°C are dried at 160°C for 5 hours in a hot air dryer.
After setting the moisture content in the particles to 0.01% by weight, a pipe-shaped molded product with an outer diameter of 11 mm and a wall thickness of approximately 1 mm was extruded using an extruder at 270°C, and immediately cooled with water to form a pipe with good transparency. . Next, this pipe is immersed in hot water at 90°C, stretched approximately 1.5 times in the axial direction, expanded horizontally by approximately 8 times with pressurized air blown into the pipe, and immediately cooled to reduce the diameter to approximately 1.5 times. A cylindrical thin film of 85 mm and wall thickness of about 0.08 mm was obtained. After printing on the surface of the film, the width is approximately 80 mm.
After cutting the thin cylindrical film into pieces of 1.5 mm and covering the outside of the body of the bottle obtained by the above method with an outer diameter of 82 mm, hot air at about 100°C was blown to shrink the cylindrical thin film. A label was attached to the section. Table 1 shows the results of experiments conducted in the same manner as above, with various molding conditions and shrinkage conditions for cylindrical thin films.

【衚】 脚台固有粘床0.68、軟化点260℃、ガラス転䜍
枩床80℃、肉厚mmのポリ゚チレンテレフタレ
ヌト補シヌトを玄100℃に加熱したのち真空成
圢により円筒郚の内埄玄82mm、底郚の圢状第
図のに瀺す劂き脚台を成圢した。 脚台のボトルぞの取り付け テレフタル酞、アゞピン酞及び゚チレングリコ
ヌルを觊媒の存圚䞋高真空にお重瞮合せしめおテ
レフタル酞アゞピン酞成分の比率が、軟
化点151℃の共重合ポリ゚ステルを埗た。 該共重合ポリ゚ステルを溶融せしめ、脚台に付
着せしめ、盎ちにボトルを装着后、冷华固化する
事により脚台をボトルぞ取付けた。 たた、ボトルぞ脚台を装着せしめた埌、脚台の
倖偎から盎埄mmの先端が平滑な200℃に加熱さ
れたステンレス補金属棒を玄秒間抌し付け脚台
の郚を軟化せしめおボトルに装着せしめる方法
も可胜であ぀た。 栓極限粘床0.85、軟化点258℃のポリ゚チレン
テレフタレヌト粒子を熱颚也燥したのち、射出
成圢機により内偎がネゞ状、倖偎が円筒状を有
する金型を甚いお栓状成圢品を金型枩床10
℃、シリンダヌ蚭定枩床265〜280℃成圢し
た。次いで別途成圢した肉厚mmのゞメチルテ
レフタレヌト、゚チレングリコヌル及びポリテ
トラメチレングリコヌル平均分子量800を
觊媒の存圚䞋゚ステル亀換反応及び高真空䞋に
重瞮合せしめたポリテトラメチレングリコヌル
30重量を含有するブロツク共重合䜓補シヌト
を円圢状に打ち抜いたものを前蚘栓内に内蓋ず
しお挿入せしめポリ゚ステル補栓を䜜成した。 かくしお埗られた、第図に瀺す劂き容噚を党
量粉砕機により粉砕したのち、也燥后前述のボト
ル及び射出成圢機により肉厚mmのテストピヌス
を成圢した。成圢品の物性を衚−に瀺す。 同様に長さmmのガラス繊維を15混合しお、
抌出機により盎埄玄mmのストランドを抌し出
し、長さmm皋床に切断しおガラス繊維入りのペ
レツトを埗た。次いで射出成圢機により肉厚0.5
mmの板状サンプルを成圢した。成圢品の物性を衚
−に瀺す。 前述の粉砕物を也燥后、抌出機により倪さ0.2
mmの糞状抌出成圢品を成圢した。成圢状況を衚−
に瀺す。 比范のために、垂販のシペり油甚ポリ゚ステル
ボトルを良く掗浄したのち、ポリ゚チレン補栓ず
玙ラベルを剥離させた埌、粉砕機により粉砕した
堎合、及び栓ず玙ラベルをそのたたにしお粉砕し
た堎合に぀いお前蚘ず同様の成圢を実斜した。 結果を衚−に瀺す。 曎に、米囜においお垂販されおいる炭酞飲料甚
PETボトルず同様のポリ゚チレン補脚台、玙ラ
ベル、アルミニりム補栓付容噚に関しおも同様の
成圢を詊みた。その結果を衚−に瀺す。
[Table] Leg stand: A polyethylene terephthalate sheet with an intrinsic viscosity of 0.68, a softening point of 260°C, a glass transition temperature of 80°C, and a wall thickness of 2 mm is heated to approximately 100°C and then vacuum formed to create a cylindrical portion with an inner diameter of approximately 82 mm and a bottom shape. 1st
A footrest as shown in Figure 3 was molded. Attaching the footrest to the bottle: A copolymerized polyester made by polycondensing terephthalic acid, adipic acid, and ethylene glycol in a high vacuum in the presence of a catalyst, with a terephthalic acid/adipic acid component ratio of 1/1 and a softening point of 151°C. I got it. The copolymerized polyester was melted and adhered to the base, and immediately after the bottle was attached, the base was attached to the bottle by cooling and solidifying. In addition, after attaching the leg to the bottle, a stainless steel metal rod with a 6 mm diameter and a smooth tip heated to 200°C was pressed from the outside of the leg for about 5 seconds to soften part of the leg and attach it to the bottle. A method of attaching it was also possible. Plug: After drying polyethylene terephthalate particles with an intrinsic viscosity of 0.85 and a softening point of 258°C with hot air, a plug-shaped molded product is produced using an injection molding machine with a mold that has a screw-like shape on the inside and a cylindrical shape on the outside (mold temperature: 10°C).
℃, cylinder set temperature 265-280℃) was molded. Next, dimethyl terephthalate, ethylene glycol, and polytetramethylene glycol (average molecular weight 800), which were separately molded with a wall thickness of 1 mm, were transesterified in the presence of a catalyst and polytetramethylene glycol was polycondensed under high vacuum.
A polyester stopper was prepared by punching out a block copolymer sheet containing 30% by weight into a circular shape and inserting it into the stopper as an inner lid. The entire container thus obtained as shown in FIG. 1 was pulverized using a pulverizer, and after drying, a test piece with a wall thickness of 2 mm was molded using the bottle and injection molding machine described above. Table 2 shows the physical properties of the molded product. Similarly, 15% of glass fiber with a length of 3 mm was mixed,
A strand with a diameter of about 2 mm was extruded using an extruder and cut into lengths of about 2 mm to obtain glass fiber-containing pellets. Next, the wall thickness is 0.5 using an injection molding machine.
A plate-shaped sample of mm was molded. Table 2 shows the physical properties of the molded product. After drying the above-mentioned pulverized material, use an extruder to reduce the thickness to 0.2
A thread-like extrusion molded product of mm was molded. Show molding status
Shown in 2. For comparison, after thoroughly washing a commercially available polyester bottle for soybean oil, and then peeling off the polyethylene stopper and paper label, the cases were crushed using a crusher, and the cases were crushed with the stopper and paper label intact. The same molding as above was carried out. The results are shown in Table-2. Furthermore, for carbonated drinks sold in the United States,
Similar molding was attempted for containers with polyethylene bases, paper labels, and aluminum stoppers similar to PET bottles. The results are shown in Table-2.

【衚】【table】

【衚】 以䞊に瀺す劂く、本発明のポリ゚ステル容噚に
よれば䜿甚枈みの空容噚を煩雑な分離操䜜を省略
或いは党く行う事なく再生利甚し埗る。
[Table] As shown above, according to the polyester container of the present invention, used empty containers can be recycled without complicated separation operations or at all.

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

第図は栓・内蓋・ラベル・脚台付き容噚の郚
分偎面及び郚分断面を瀺す図である。第図は
栓・内蓋・ラベル及び把手付容噚の郚分偎面及び
郚分断面を瀺す図である。第図はボトル底郚に
脚台を接合した状態を瀺す郚分偎面及び郚分断面
図である。第図はボトル底郚に脚台を熱接着し
た状態を瀺す郚分偎面及び郚分断面図である。
FIG. 1 is a partial side view and partial cross-sectional view of a container with a stopper, an inner lid, a label, and a base. FIG. 2 is a partial side view and partial cross-sectional view of a container with a stopper, an inner lid, a label, and a handle. FIG. 3 is a partial side view and a partial sectional view showing a state in which the leg base is joined to the bottom of the bottle. FIG. 4 is a partial side view and a partial cross-sectional view showing a state in which the leg base is thermally bonded to the bottom of the bottle.

Claims (1)

【特蚱請求の範囲】  容噚本䜓が゚チレンテレフタレヌトを䞻たる
繰り返し単䜍ずするポリ゚ステルよりなり、該
容噚の栓、蓋、把持甚把手及び脚台よりなる構成
郚分の材質が金属材料を陀き゚チレンテレフタレ
ヌトを䞻たる繰り返し単䜍ずするポリ゚ステル
よりなり、か぀該容噚が゚チレンテレフタレヌト
を䞻たる繰り返し単䜍ずするポリ゚ステルより
なる収瞮された筒状薄葉䜓からなるラベルを付さ
れおなるポリ゚ステル容噚。  ゚チレンテレフタレヌトを䞻たる繰り返し単
䜍ずするポリ゚ステルよりなる容噚本䜓の胎郚
に、゚チレンテレフタレヌトを䞻たる繰り返し単
䜍ずするポリ゚ステルのラベルを装着するに際
し、その密床が1.38cm3以䞋でありか぀面配向
床が0.02以䞊の筒状薄葉䜓を前蚘胎郚の倖偎にか
ぶせ、該薄葉䜓を構成する該ポリ゚ステルのガ
ラス転移枩床以䞊の枩床で該薄葉䜓を収瞮させお
ラベル化するこずを特城ずするポリ゚ステル容噚
の補造法。
[Scope of Claims] 1. The main body of the container is made of polyester A containing ethylene terephthalate as a main repeating unit, and the materials of the component parts of the container, including the stopper, lid, gripping handle, and footrest, do not contain ethylene terephthalate, except for metal materials. Polyester B as the main repeating unit
1. A polyester container comprising a label made of a shrunken cylindrical thin film made of polyester C whose main repeating unit is ethylene terephthalate. 2. When attaching a label made of polyester C, whose main repeating unit is ethylene terephthalate, to the body of a container body made of polyester A, whose main repeating unit is ethylene terephthalate, it must have a density of 1.38 g/cm 3 or less and a surface area of 1.38 g/cm 3 or less. A cylindrical thin film body having an orientation degree of 0.02 or more is placed over the outside of the body, and the thin film body is shrunk at a temperature equal to or higher than the glass transition temperature of the polyester C constituting the thin film body to form a label. A method for manufacturing polyester containers.
JP6340881A 1981-04-28 1981-04-28 Polyester vessel and its manufacture Granted JPS57194950A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6340881A JPS57194950A (en) 1981-04-28 1981-04-28 Polyester vessel and its manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6340881A JPS57194950A (en) 1981-04-28 1981-04-28 Polyester vessel and its manufacture

Publications (2)

Publication Number Publication Date
JPS57194950A JPS57194950A (en) 1982-11-30
JPS6340747B2 true JPS6340747B2 (en) 1988-08-12

Family

ID=13228438

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6340881A Granted JPS57194950A (en) 1981-04-28 1981-04-28 Polyester vessel and its manufacture

Country Status (1)

Country Link
JP (1) JPS57194950A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6291555A (en) * 1985-10-18 1987-04-27 Toyobo Co Ltd Heat-shrinkable polyester film
JPS6292826A (en) * 1985-10-18 1987-04-28 Toyobo Co Ltd Heat-shrinkable polyester-based tube
KR960000590B1 (en) * 1986-11-12 1996-01-09 닀읎아혞음 가부시끌가읎샀 Shrinkable polyester film
US4983653A (en) * 1986-11-12 1991-01-08 Diafoil Company, Ltd. Polyester shrinkable film containing benzotriazole
JPH0618902B2 (en) * 1986-12-19 1994-03-16 東掋玡瞟株匏䌚瀟 Heat-shrinkable polyester film
JPH0618903B2 (en) * 1986-12-25 1994-03-16 東掋玡瞟株匏䌚瀟 Heat-shrinkable polyester film

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
JOURNAL OF PO1YMER SCIENCE POLYMER SYMPOSIUM58=1977 *

Also Published As

Publication number Publication date
JPS57194950A (en) 1982-11-30

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