JPS60165221A - Manufacture of polypropylene sheet for press through package - Google Patents

Manufacture of polypropylene sheet for press through package

Info

Publication number
JPS60165221A
JPS60165221A JP59019382A JP1938284A JPS60165221A JP S60165221 A JPS60165221 A JP S60165221A JP 59019382 A JP59019382 A JP 59019382A JP 1938284 A JP1938284 A JP 1938284A JP S60165221 A JPS60165221 A JP S60165221A
Authority
JP
Japan
Prior art keywords
polypropylene
resin
sheet
annealing
package
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP59019382A
Other languages
Japanese (ja)
Other versions
JPH0442179B2 (en
Inventor
Katsuyuki Usami
宇佐美 勝幸
Toru Ueki
徹 植木
Hajime Chitoku
千徳 一
Takashi Takahashi
孝 高橋
Kazuharu Kanezaki
金崎 和春
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP59019382A priority Critical patent/JPS60165221A/en
Publication of JPS60165221A publication Critical patent/JPS60165221A/en
Publication of JPH0442179B2 publication Critical patent/JPH0442179B2/ja
Granted 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
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/911Cooling
    • B29C48/9135Cooling of flat articles, e.g. using specially adapted supporting means
    • 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
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • 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
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/10Polymers of propylene
    • B29K2023/12PP, i.e. polypropylene

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Packages (AREA)

Abstract

PURPOSE:To obtain the polypropylene sheet excellent in transparence, theremoforming property and safety by annealing the resin composition composed of 100pts.wt. polypropylene and 3-20pts.wt. hydrogenated petrol resin at the temperature equal to or higher than 50 deg.C for 30min or more, after said resin composition has been extruded. CONSTITUTION:The hydrogenated petrol resin of 3-20pts.wt., preferably 6- 11pts.wt., to 100pts.wt. polypropylene resin is preliminarily blended with polypropylene stabilizer by a Henschel mixer, etc. After said blended resin has been extruded into a resin composition by a extruder, etc. it is sheeted by a T die process, etc. Its annealing is carried out at the annealing temperature equal to or higher than 50 deg.C, preferably at the range of 80-130 deg.C, for 30min or more, preferably for 60min or more. Thus obtained sheet for PTP package is excellent in the resistance for permeability of moisture, transparence and safety, and further excellent in also thermoforming property at TPT package.

Description

【発明の詳細な説明】 用されているプレススルーパノク包装(以下、FTP包
装と略記する)に適した透明性、熱成形性、安全性に優
れたポリプロピレンシートの製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a polypropylene sheet that has excellent transparency, thermoformability, and safety and is suitable for press-through packaging (hereinafter abbreviated as FTP packaging).

従来、FTP包装には硬質塩化ビニル慎j脂シート(以
下、塩ビシートと略記する)が主に使用されている。し
かしながら、塩ビシートはアスピリン、抗生物質等の湿
気により変質し易い医薬品に対してはその透湿度が太き
すぎ、史に透湿度の小さいポリ塩化ビニリデン等を積層
して使用され、そのため高価となる欠点がある。それ故
により安価で透湿准の小さいPTI)包装用シートの出
現が望まれている。
Conventionally, hard vinyl chloride plastic sheets (hereinafter abbreviated as PVC sheets) have been mainly used for FTP packaging. However, the moisture permeability of PVC sheets is too high for pharmaceuticals that are susceptible to deterioration due to moisture, such as aspirin and antibiotics. There are drawbacks. Therefore, the emergence of a packaging sheet (PTI) that is cheaper and has lower moisture permeability is desired.

一方、ポリプロピレンシートは、その透湿度が塩ビシー
トより小さいにもかかわらず、透明性、熱成形性に問題
があり、PTP包装にはほとんど使用されていないのが
現状である。
On the other hand, although polypropylene sheets have lower moisture permeability than PVC sheets, they have problems with transparency and thermoformability, and are currently hardly used in PTP packaging.

ところて゛ポリプロピレンシートの透明性を改良する方
法としては、ポリプロピレンにジベンジリテンソルビト
ール青の造核剤を添刀目する方法か、また熱成形性を改
良する方法としては、ポリプロピレンにポリエチレンを
ブレンドする方法が知ら1tているがいずれにおいても
長短があり、例えば前者においては成形性が悪く、後者
においては透明性が悪く、FTP包装に使用するには問
題がある。
However, one way to improve the transparency of polypropylene sheets is to add dibenzylitensorbitol blue nucleating agent to polypropylene, and one way to improve thermoformability is to blend polypropylene with polyethylene. However, each type has its advantages and disadvantages; for example, the former has poor moldability, and the latter has poor transparency, which poses problems for use in FTP packaging.

ポリプロピレンシートの透明性と熱成形性を同時に改良
する方法としては、ポリプロピレンに水素化/ν るが、この方法で得られるシートはノルマへブタハ ン(以下1.、−f(Tと略記する)溶出量が多く、厚
生省告示第20号の規準(150ppm以下)を満足し
ないものが多く、実質上使用できないのが実状である。
A method for simultaneously improving the transparency and thermoformability of a polypropylene sheet is to hydrogenate the polypropylene, but the sheet obtained by this method is eluted with butahan (hereinafter referred to as 1., -f (abbreviated as T)). The amount is so large that many do not meet the standards (150 ppm or less) of the Ministry of Health and Welfare Notification No. 20, and the reality is that they are virtually unusable.

本発明者らは、上記問題を解決すべく鋭意検討し1こ結
果、上記シートを特定の温度以上で特定の時間以上アニ
ール処理すれば、厚生省告示第20号の基準を満足する
シートが得られることを見出し、本発明に到達した。
The inventors of the present invention have conducted extensive studies to solve the above problem, and have found that if the sheet is annealed at a temperature above a certain level for a certain period of time, a sheet that satisfies the standards of Ministry of Health and Welfare Notification No. 20 can be obtained. They discovered this and arrived at the present invention.

すなわち、本発明は、ポリプロピレフ100重量部と水
素化石油樹脂の3〜20重量部からなる樹脂組成物を押
出成形した後、50℃以上の温度で30分以上アニール
することを特徴とするプレススルーパック包装用ポリプ
ロピレンシートの製造方法である。
That is, the present invention provides a press characterized in that after extrusion molding a resin composition consisting of 100 parts by weight of polypropylene and 3 to 20 parts by weight of hydrogenated petroleum resin, the resin composition is annealed at a temperature of 50° C. or higher for 30 minutes or more. This is a method for manufacturing polypropylene sheets for through-pack packaging.

本発明において、ポリプロピレンとしては、ホモポリプ
ロピレン、プロピレンとエチレン、ブテン−1等のα−
オレフィンとのランダム共重合体が使用可能である。な
かでもJIS K7210の乗件14で測定したメルト
フローインデックス(以下MIと略記する。単位l/1
o分)が1〜4のものが、さらにホモポリプロピレンが
透明性及び成形性のバランス上好ましい。+nIが1未
満では透明性が悪(なり、IVIが4を越えると熱成形
時にべとつき、成形性が悪くなる。
In the present invention, polypropylene includes α-polypropylene, propylene and ethylene, butene-1, etc.
Random copolymers with olefins can be used. Among them, the melt flow index (hereinafter abbreviated as MI, unit: l/1) measured according to Multiplicity 14 of JIS K7210.
Polypropylene having an o content of 1 to 4 is preferable, and homopolypropylene is preferable in view of the balance between transparency and moldability. If +nI is less than 1, the transparency will be poor, and if IVI is more than 4, it will become sticky during thermoforming, resulting in poor moldability.

本発明において使用する水素化石油樹脂とは、芳香族炭
化水系の水素化物、テルペン樹脂の水素化物等であり、
具体的にはスチレン、α−メチルスチレン、ビニルトル
エン、ビニルキシレン、プロペニルベンゼン、インデン
、メチルインデン、エチルインデン等の各種の芳香族不
飽オロ炭fヒ水素及び/又はテルペン類の1種又は2種
以上の混合物を主体として重合して得られる樹脂を水素
化したものや石油の分解、改質の原に副生ずる沸点20
−300℃、とくに150〜300℃の留分を重合して
得られる樹脂を水素化したものがあげられる。なかでも
JIS K5902の環球法で測定した軟化点が124
℃以上の芳香族炭化水系の水素化物はπ−HT浴出量が
少な(好ましい。
The hydrogenated petroleum resin used in the present invention is an aromatic hydrocarbon hydride, a terpene resin hydride, etc.
Specifically, one or two of various aromatic unsaturated orocarbons such as styrene, α-methylstyrene, vinyltoluene, vinylxylene, propenylbenzene, indene, methylindene, and ethylindene, arsenic, and/or terpenes. Hydrogenated resin obtained by polymerizing a mixture of more than 1 species, boiling point 20 as a by-product of petroleum decomposition and reforming.
Examples include hydrogenated resins obtained by polymerizing fractions at -300°C, particularly from 150 to 300°C. Among them, the softening point measured by the JIS K5902 ring and ball method is 124.
Aromatic hydrocarbon-based hydrides with a temperature of .degree. C. or higher have a small amount of .pi.-HT bathed out (preferably).

本発明において、水素化石油樹脂の使用量は、その軟化
点により異なるが、ポリプロピレン100重電部に対し
6〜20重量部、好ましくは6〜11重量部である。そ
の使用量が3重量部未満では、透明性、熱成形性の改良
効果が不充分であり、逆に20重量部を越して使用する
と、熱成り1*性が悪くなる。
In the present invention, the amount of hydrogenated petroleum resin used varies depending on its softening point, but is 6 to 20 parts by weight, preferably 6 to 11 parts by weight, based on 100 parts by weight of polypropylene. If the amount used is less than 3 parts by weight, the effect of improving transparency and thermoformability will be insufficient, and if it is used in excess of 20 parts by weight, the heat build-up 1* property will deteriorate.

本発明において、ポリプロピレンと水素化石油樹脂は、
予め、ポリプロピレン用安定剤とともに、ヘンシェルミ
キサー等の公知の機械で配合し、押出機等の公知の機械
で樹脂組成物とし、しかる後Tダイ法等の公知の方法で
シートとし、さらにアニール処理される。
In the present invention, polypropylene and hydrogenated petroleum resin are
It is mixed in advance with a stabilizer for polypropylene using a known machine such as a Henschel mixer, made into a resin composition using a known machine such as an extruder, then formed into a sheet using a known method such as the T-die method, and then annealed. Ru.

本発明においては、シート化したのちのアニール処理が
重要であり、そのアニール温度は50℃以上、好ましく
は80〜130℃である。50℃未満では、、−HT溶
出抑制効果が不充分であり、溶出量が多くなる。又、ア
ニールの時間は60分以上、より好ましくは60分以上
である。30分未満ではアニールの効果が不充分であり
、7L −H’l’溶出量が多くなる。
In the present invention, annealing treatment after forming into a sheet is important, and the annealing temperature is 50°C or higher, preferably 80 to 130°C. Below 50°C, the effect of suppressing -HT elution is insufficient and the amount of elution increases. Further, the annealing time is 60 minutes or more, more preferably 60 minutes or more. If the time is less than 30 minutes, the annealing effect will be insufficient and the amount of 7L-H'l' elution will increase.

こうして得られたFTP包装用シートは、耐透湿性、透
明性、安全性に優れ、且つ、FTP包装時の熟成形性に
も優れたシートであり、FTP包装用の成形機にかけら
れ実用に供せられる。
The FTP packaging sheet obtained in this way has excellent moisture permeability, transparency, and safety, and also has excellent aging formability during FTP packaging, and can be put into practical use by being put into a molding machine for FTP packaging. be given

なお、P’I”l)包装とは、錠剤、カプセル等をプラ
スチックシートのポケットとそれをシールするアルミ箔
で包装する包装形態であり、通常、熱可塑性シートを熱
成形し、これに錠剤、カプセル等を自動充填し、アルミ
箔でシールし、ミシン目、スリフトを入れ、外周を打抜
くまでの工程を連続的におこなう高速自動包装機械を使
用して実施されている。
Note that P'I"l) packaging is a form of packaging in which tablets, capsules, etc. are packaged with a plastic sheet pocket and aluminum foil that seals the pocket. Usually, a thermoplastic sheet is thermoformed and the tablets, capsules, etc. This is done using a high-speed automatic packaging machine that continuously performs the steps of automatically filling capsules, etc., sealing with aluminum foil, making perforations and thrifts, and punching out the outer periphery.

本発明の製造方法で得られるP’ll”P包装用シート
は、熱成形時の成形性が優れており、且つ、アルミ箔と
の熱接着性、打抜き性にも優れている為、偏肉の少ない
浸れたFTP包装品が高速で得られる。
The P'll"P packaging sheet obtained by the production method of the present invention has excellent formability during thermoforming, and also has excellent thermal adhesion with aluminum foil and punching properties, so it has no uneven thickness. Soaked FTP packaged products with less water can be obtained at high speed.

又、得られたFTP包装品の品質も、透明性、耐透湿性
、安全性ともに優れたものである。
Furthermore, the quality of the obtained FTP packaged product is excellent in terms of transparency, moisture permeability, and safety.

以下、実施例により本発明を更に説明する。The present invention will be further explained below with reference to Examples.

実施例1 ジターシャリブチル−p〜クレゾール01重量部、ステ
アリン酸カルシウム01重量部が配合された+VI=2
のホモポリプロピレン100重Jlt(克 に、軟化色125℃の水素化石油樹脂を10重量部配合
し、ヘンシェルミキサーで混合した後、シリンダー径d
Qmmの押出機を使用して240℃で押出しペレットと
した。
Example 1 Ditert-butyl-p~cresol 01 parts by weight, calcium stearate 01 parts by weight were blended +VI=2
10 parts by weight of homopolypropylene 100 weight Jlt (exactly) was blended with 10 parts by weight of hydrogenated petroleum resin with a softening color of 125°C, and after mixing in a Henschel mixer, the cylinder diameter d
Pellets were extruded at 240° C. using a Qmm extruder.

このベレットを240℃でTダイ付きのシリンダー径4
0關の押出機でシート化し、巾200闘、厚さ0.25
 amの7−トを得た。
This pellet was heated to 240℃ with a cylinder diameter of 4 with a T die.
Made into a sheet using a 0.0-speed extruder, with a width of 200mm and a thickness of 0.25mm.
7-t of am was obtained.

次にこのシートを80℃で120分間アニールし、p’
rp包装用シートを得た。
This sheet was then annealed at 80°C for 120 minutes and p'
An RP packaging sheet was obtained.

得られたシートを株式会社カナエ製のFTP包装機*1
oooによりPTP包装を実施して成形性を評価し1こ
。また、このシートの透明性、透湿ヰ1、、− HT溶
出量も測定した。結果を表−1に示す。
The obtained sheet is passed through an FTP packaging machine manufactured by Kanae Co., Ltd. *1
PTP packaging was performed using ooo, and the moldability was evaluated. In addition, the transparency and moisture permeability of this sheet and the amount of elution of -HT were also measured. The results are shown in Table-1.

なお、透明性はASTM−D−1o 03に従ってヘイ
ズを測定し、透湿度はASTIVi−E−96に従って
測定し1.、−HT溶出量は厚生省告示渠20号に従っ
ておこなった。
In addition, transparency was measured by measuring haze according to ASTM-D-1o 03, and moisture permeability was measured according to ASTIVi-E-96. , -HT elution amount was determined in accordance with Ministry of Health and Welfare Notification No. 20.

実施例2,6及び比較例1〜5 実施例1において、アニール温度を表−1のとおりにか
えた他は同様にしてシートを得た。得られたシートの諸
物性および成形性を評価した。結果を表−1に示す。
Examples 2 and 6 and Comparative Examples 1 to 5 Sheets were obtained in the same manner as in Example 1, except that the annealing temperature was changed as shown in Table 1. The various physical properties and moldability of the obtained sheet were evaluated. The results are shown in Table-1.

実施例4〜6及び比較例4 実施例1において、アニール時間を表−1のとおりにか
えた他は同様にシートを得1こ。得られたシートの諸物
性および成形性を評価した。結果を表−1に示す。
Examples 4 to 6 and Comparative Example 4 A sheet was obtained in the same manner as in Example 1 except that the annealing time was changed as shown in Table 1. The various physical properties and moldability of the obtained sheet were evaluated. The results are shown in Table-1.

実施例48及び比較例5.6 実施例ろにおいて、表−1の軟化点を有する水素化石油
樹脂を表−1の量使用する他は、実施例3と同様にして
シートを得た。得られたシートの諸物性および成形性を
評価した。結果を表−1に示す。
Example 48 and Comparative Examples 5.6 Sheets were obtained in the same manner as in Example 3, except that the hydrogenated petroleum resin having the softening point shown in Table 1 was used in the amount shown in Table 1. The various physical properties and moldability of the obtained sheet were evaluated. The results are shown in Table-1.

Claims (1)

【特許請求の範囲】 1ポリプロピレン100重量部と水素化石油樹脂3〜2
0重量部からなる樹脂組成物を押出成形した後、50℃
以上の温度で60分以上アニールすることを特徴とする
プレススルーパック包装用ポリプロピレンシートの製造
方法。 2水素化石油樹脂が軟化点124℃以上のものである特
許請求の範囲、第1項記載の製造方法。
[Claims] 1 100 parts by weight of polypropylene and 3 to 2 parts of hydrogenated petroleum resin
After extrusion molding a resin composition consisting of 0 parts by weight, 50°C
A method for producing a polypropylene sheet for press-through pack packaging, characterized by annealing at a temperature above 60 minutes or more. The manufacturing method according to claim 1, wherein the dihydrogenated petroleum resin has a softening point of 124° C. or higher.
JP59019382A 1984-02-07 1984-02-07 Manufacture of polypropylene sheet for press through package Granted JPS60165221A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59019382A JPS60165221A (en) 1984-02-07 1984-02-07 Manufacture of polypropylene sheet for press through package

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59019382A JPS60165221A (en) 1984-02-07 1984-02-07 Manufacture of polypropylene sheet for press through package

Publications (2)

Publication Number Publication Date
JPS60165221A true JPS60165221A (en) 1985-08-28
JPH0442179B2 JPH0442179B2 (en) 1992-07-10

Family

ID=11997755

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59019382A Granted JPS60165221A (en) 1984-02-07 1984-02-07 Manufacture of polypropylene sheet for press through package

Country Status (1)

Country Link
JP (1) JPS60165221A (en)

Also Published As

Publication number Publication date
JPH0442179B2 (en) 1992-07-10

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