JPS6236062B2 - - Google Patents

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Publication number
JPS6236062B2
JPS6236062B2 JP54015340A JP1534079A JPS6236062B2 JP S6236062 B2 JPS6236062 B2 JP S6236062B2 JP 54015340 A JP54015340 A JP 54015340A JP 1534079 A JP1534079 A JP 1534079A JP S6236062 B2 JPS6236062 B2 JP S6236062B2
Authority
JP
Japan
Prior art keywords
sheet
polyethylene
weight
mfr
polypropylene
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
JP54015340A
Other languages
Japanese (ja)
Other versions
JPS55108433A (en
Inventor
Koji Nishida
Jun Maeda
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Petrochemical 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 Mitsubishi Petrochemical Co Ltd filed Critical Mitsubishi Petrochemical Co Ltd
Priority to JP1534079A priority Critical patent/JPS55108433A/en
Publication of JPS55108433A publication Critical patent/JPS55108433A/en
Publication of JPS6236062B2 publication Critical patent/JPS6236062B2/ja
Granted legal-status Critical Current

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  • Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はシートの深絞りにより容器を成形する
技術におけるオレフイン重合体シートに関するも
のである。更に詳しくは真空又は圧空成形におい
て成形する際、広範囲温度にわたり安定に成形で
き、かつ肉厚ムラなく深く絞れた容器が得られる
シートに関するものである。 従来、かかる成形用樹脂としてポリスチレン、
ハイインパクトポリスチレン、ABS、塩化ビニ
ール等、非結晶性樹脂が使用されてきた。しかし
最近、例えばかかる成形用樹脂成分に含まれるモ
ノマーの毒性、可塑剤の溶出及び配合されるゴム
成分中の充填物の衛生性等の問題により、この様
な懸念のないポリオレフイン系樹脂の出現が要望
されていた。 一般にポリエチレン、ポリプロピレン等単体の
ポリオレフイン樹脂は結晶性樹脂の為、融点以下
では深く絞るのが困難であり、たとえ出来ても、
成形品は経日と共に歪回復するので結果として深
絞りできないこととなる。一方融点以上では樹脂
の粘度が急激に低下し、温度変化も大きいのでシ
ートの平面及び厚み方向の各場所に於る粘度が異
なり、成形品の厚みムラが大きくなるといつた欠
点がある。 本発明はポリエチレン、ポリプロピレン各々単
独組成のシートのかかる欠点を改良したものであ
る。 すなわち、本発明はメルトフローレイト2.0
g/10分以下のポリエチレン95〜50重量%および
メルトフローレイト3.0g/10分以下のアイソタ
クチツクポリプロピレン5〜50重量%とからなる
組成物を常法により延伸工程を経ることなしに成
形したシートであり、かかるシートは、厚みムラ
のない深絞り容器の製造に好適であり、このシー
トを用いて後述する成形法により深絞りを行なつ
た場合、安定して成形できる温度範囲が広く、厚
みムラのない成形品を得ることができる。 本発明シートから得た容器は食品、冷菓、乳酸
飲料など前述の問題の解決が厳しく要求される用
途は勿論のこと、その他の物品や液体の充填用途
に使用することが出来る。 また本発明シートは鋳造のVプロセスに於い
て、砂型を安定にし、かつ鋳物への砂の進入防止
を目的として用いられる砂型と同形に絞られたシ
ート状の膜の如き用途にも利用できる。 またシート片面に接着剤や粘着剤を塗布して深
絞りをし、紙や金属等他の材料で出来た容器に同
時積層させる技術におけるシートとしても、本発
明シートが利用できる。 本発明で使用するメルトフローレイト2.0g/
10分以下のポリエチレンとは高圧法又は配位型触
媒により製造しうるエチレンの単独重合体または
共重合体であり、かかる共重合体の共重合モノマ
ーとしてはプロピレン、n−ブテン−1、n−ペ
ンテン−1、n−ヘキセン−1、n−ヘプテン−
1、n−オクテン−1、n−デセン−1、4メチ
ルペンテン−1の如き炭素数3〜20のαオレフイ
ンを挙げることができる。かかる重合体は上記共
重合モノマーの2種以上のものとエチレンとの共
重合体であつてもよいが、エチレン含量が少なく
とも50重量%以上のものである。この場合ポリエ
チレンのメルトフローレイト(以下MFRと記載
する)の測定法はJIS K 6760に準拠するもので
ある。MFRに制限があるのは、2.0g/10分超過
のMFRではシート加熱時のタレ下りが大きくな
る事及び成形品の厚みムラが大きくなる為であ
る。 MFRの下限界については、実質上流動性のな
いポリエチレンでも成形機によつてシートに成形
されるものであればよく、実際上は限界がないと
云える。 また、本発明で使用するメルトフローレイト
3.0g/10分以下のアイソタクチツクポリプロピ
レンとは配位型触媒によつて製造しうるプロピレ
ンの単独重合体もしくはプロピレンと炭素数2及
び4〜20のαオレフインとのブロツク共重合体な
いしランダム共重合体(プロピレン含量50重量%
以上のもの)をも含み、沸騰ヘプタン抽出量60重
量%以下の結晶性を有するものである。ポリプロ
ピレンのMFRの測定法はJIS K 6758に準拠す
るものである。MFRがこれより大きい場合、シ
ートのタレ下りが大きくかつ成形品の厚みムラも
大きくなる。MFRの下限界についてはポリエチ
レンのそれと同様である。本発明で使用するかか
るポリエチレンおよびポリプロピレンの配合割合
はポリエチレン95〜50重量%およびポリプロピレ
ン5〜50重量である。組成に於る制限はポリエチ
レン含量をポリプロピレン含量と同等もしくはそ
れ以上にする事が必要であり、ポリプロピレンが
ポリエチレンより多い系ではポリプロピレン単独
の場合と同様な結果となり深絞りができない。又
ポリプロピレン5重量%未満では改良効果がな
い。 本発明シートの組成物であるかかるポリエチレ
ンとポリプロピレンとの配合組成物は公知のブレ
ンド手法、例えば押出機、バンバリー、ロール、
ブラベンダープラストグラムなどの混練機を用い
て得られる。通常は押出機などで混練して一旦ペ
レツト状コンパウンドにした後、シート加工に供
するが、上記のポリエチレンとポリプロピレンの
2成分をドライブレンド等により直接シート成形
することもできる。本発明シートの組成物には酸
化防止剤、耐候性改良剤、帯電防止剤、滑剤、顔
料等の添加剤を併用する事も勿論可能である。 深絞りに供する本発明シートは通常の成形法で
成形される。例えば、Tダイを用いた押出成形、
プレス成形、カレンダー成形等の成形法により得
られるが、薄物の場合はインフレーシヨン成形等
によつても得ることができる。 次に実施例を示すが、成形品の厚みムラおよび
厚みムラの起らない成形温度範囲の評価方法は次
の方法に拠つた。 試験体である150μ厚さのシートを250mm×250
mm×3mmで150mm径の中央孔を有する板状の2枚
のアルミ枠の間に挾み、圧空成形機に水平にセツ
トする。次に圧空成形機の350〜450℃に加熱され
たヒーターをシート上面15cmの高さにスライドさ
せる。シートが加熱され半透明から透明の状態に
なつたらヒーターを取除き先端R40mmでフエルト
を巻いた押込プラグを押込速度300mm/secで210
mm深さに押込む。絞り比は1.4である。冷却後押
込プラグを抜取り成形品の押込方向及び円周方向
の厚みムラを評価する。 又、シートの上面にサーモテープを貼りその色
の変化によつて、厚みムラのない成形品が得られ
る成形可能な温度範囲を評価する。 実施例 1 MFR2.0g/10分、密度0.950のポリエチレンペ
レツトにMFR3.0g/10分のプロピレンホモポリ
マーペレツトを5、10、20、30、40、50、60、80
重量%添加した組成物について、ヘンシエルミキ
サーでブレンドし、Tダイ成形機(スクリユー径
35mm、L/D=22)にて、成形温度230℃で150μ
厚さのシートに成形し、各種項目について検討し
た。ポリエチレン、プロピレンホモポリマー各単
独の場合と比較した結果を表1に示す。これより
ポリエチレンにポリプロピレンを5〜50重量%、
望ましくは10〜40重量%添加すれば安定的に成形
が出来、厚みムラのない成形品が得られる事が判
明した。 実施例 2 MFR0.03、1.0、2.0、3.0のポリエチレン50重
量%に対しMFR3.0g/10分のプロピレンホモポ
リマー50重量%添加した組成物について実施例1
と同様な方法でシート化し、各種検討した。その
結果ポリエチレンのMFRとしては可及的に低い
ことが望ましく、MFR2.0g/10分超過ではシー
トのタレ下りが大きく、かつ厚みムラが目立つよ
うになる。表2に結果を纒めた。 実施例 3 MFR2.0g/10分で密度0.954g/cm3のポリエチ
レン50重量%に対し、MFR0.05、3.0、4g/10
分のプロピレンホモポリマーMFR3.0g/10分で
エチレン含量15重量%を有するプロピレンとエチ
レンとのブロツク共重合体及びMFR3.0g/10分
でエチレン含量3.5重量%を有する結晶性プロピ
レン−エチレンランダム共重合体各50重量%添加
した組成物について実施例1と同様な方法でシー
ト化し、各種検討した。結果を表3に示す。 これより配合するポリプロピレンについても低
MFRが望ましく、MFR3.0g/10分超過ではシー
トのタレ下りが大きく、厚みムラも大であつた。
ポリプロピレンのMFRは3.0g/10分以下に制限
される。更にポリプロピレンとしては単独、ブロ
ツク、ランダム共重合体のいずれでも同様な効果
が確認された。
The present invention relates to an olefin polymer sheet used in the technique of forming containers by deep drawing the sheet. More specifically, the present invention relates to a sheet that can be stably molded over a wide range of temperatures when molded using vacuum or pressure molding, and that can yield containers that are deeply squeezed with uniform wall thickness. Conventionally, polystyrene,
Amorphous resins such as high-impact polystyrene, ABS, and vinyl chloride have been used. However, recently, due to problems such as the toxicity of monomers contained in such molding resin components, the elution of plasticizers, and the hygiene of fillers in rubber components, polyolefin resins that do not have such concerns have appeared. It was requested. In general, simple polyolefin resins such as polyethylene and polypropylene are crystalline resins, so it is difficult to squeeze them deeply below their melting point, and even if it is possible,
Since the molded product recovers from strain over time, it cannot be deep drawn as a result. On the other hand, above the melting point, the viscosity of the resin decreases rapidly and temperature changes are large, so the viscosity differs at various locations in the plane and thickness direction of the sheet, resulting in a disadvantage that the thickness unevenness of the molded product increases. The present invention improves these drawbacks of sheets made of polyethylene and polypropylene alone. That is, the present invention has a melt flow rate of 2.0.
A composition consisting of 95-50% by weight of polyethylene with a melt flow rate of 3.0 g/10 minutes or less and 5-50% by weight of isotactic polypropylene with a melt flow rate of 3.0 g/10 minutes or less was molded by a conventional method without a stretching process. This sheet is suitable for manufacturing deep-drawn containers with uniform thickness, and when this sheet is deep-drawn by the forming method described below, the temperature range in which the sheet can be formed stably is wide, A molded product with even thickness can be obtained. Containers obtained from the sheet of the present invention can be used not only for foods, frozen desserts, lactic acid drinks, and other applications where solving the aforementioned problems are strictly required, but also for filling other articles and liquids. The sheet of the present invention can also be used as a sheet-like membrane drawn into the same shape as the sand mold used in the V process of casting to stabilize the sand mold and prevent sand from entering the casting. The sheet of the present invention can also be used as a sheet in a technique in which adhesive or pressure-sensitive adhesive is applied to one side of the sheet, deep drawing is performed, and the sheet is simultaneously laminated onto a container made of other materials such as paper or metal. Melt flow rate used in the present invention: 2.0g/
Polyethylene of 10 minutes or less is an ethylene homopolymer or copolymer that can be produced by a high-pressure method or a coordination catalyst, and copolymer monomers for such a copolymer include propylene, n-butene-1, n- Pentene-1, n-hexene-1, n-heptene-1
Examples include α-olefins having 3 to 20 carbon atoms such as 1, n-octene-1, n-decene-1, and 4-methylpentene-1. Such a polymer may be a copolymer of two or more of the above copolymerizable monomers and ethylene, but the ethylene content is at least 50% by weight. In this case, the method for measuring the melt flow rate (hereinafter referred to as MFR) of polyethylene is based on JIS K 6760. There is a limit to MFR because if the MFR exceeds 2.0g/10 minutes, the sagging during sheet heating will increase and the thickness of the molded product will become more uneven. As for the lower limit of MFR, it can be said that there is no practical limit, as even polyethylene having substantially no fluidity may be formed into a sheet by a molding machine. In addition, the melt flow rate used in the present invention
Isotactic polypropylene of 3.0 g/10 minutes or less refers to a propylene homopolymer that can be produced using a coordination catalyst, or a block copolymer or random copolymer of propylene and an α-olefin having 2 or 4 to 20 carbon atoms. Polymer (propylene content 50% by weight)
(above), and has crystallinity with a boiling heptane extraction amount of 60% by weight or less. The method for measuring MFR of polypropylene is based on JIS K 6758. If the MFR is larger than this, the sag of the sheet will be large and the thickness unevenness of the molded product will also be large. The lower limit of MFR is the same as that of polyethylene. The blending ratio of such polyethylene and polypropylene used in the present invention is 95 to 50% by weight of polyethylene and 5 to 50% by weight of polypropylene. The restriction on the composition is that the polyethylene content must be equal to or higher than the polypropylene content, and in a system where the polypropylene content is greater than the polyethylene content, the result is similar to that of polypropylene alone, and deep drawing cannot be performed. Further, if the amount of polypropylene is less than 5% by weight, there is no improvement effect. The blended composition of polyethylene and polypropylene, which is the composition of the sheet of the present invention, can be prepared using known blending methods such as extruder, Banbury, roll, etc.
Obtained using a kneader such as a Brabender plastogram. Usually, the compound is kneaded in an extruder or the like to form a pellet-like compound and then processed into a sheet, but it is also possible to directly form a sheet by dry blending the two components of polyethylene and polypropylene. It is of course possible to use additives such as antioxidants, weatherability improvers, antistatic agents, lubricants, and pigments in the composition of the sheet of the present invention. The sheet of the present invention to be subjected to deep drawing is formed by a conventional forming method. For example, extrusion molding using a T-die,
It can be obtained by a molding method such as press molding or calendar molding, but in the case of a thin product, it can also be obtained by inflation molding or the like. Examples will now be shown, in which the following method was used to evaluate the thickness unevenness of the molded product and the molding temperature range in which the thickness unevenness does not occur. The test specimen, a 150μ thick sheet, was placed in a 250mm x 250
It is sandwiched between two plate-shaped aluminum frames measuring mm x 3 mm and having a central hole of 150 mm in diameter, and set horizontally in an air pressure forming machine. Next, slide the heater heated to 350 to 450°C in the pressure forming machine to a height of 15 cm above the sheet surface. When the sheet is heated and changes from translucent to transparent, remove the heater and insert a push-in plug wrapped in felt with a tip radius of 40 mm at a speed of 300 mm/sec to 210 mm.
Push to a depth of mm. The aperture ratio is 1.4. After cooling, the push-in plug is removed and the thickness unevenness of the molded product in the push-in direction and circumferential direction is evaluated. Additionally, thermo tape is applied to the top surface of the sheet, and the temperature range in which a molded product with uniform thickness can be obtained is evaluated based on the change in color. Example 1 Propylene homopolymer pellets with MFR 3.0 g/10 min were added to polyethylene pellets with MFR 2.0 g/10 min and density 0.950 at 5, 10, 20, 30, 40, 50, 60, 80
The composition containing % by weight was blended using a Henschel mixer, and the T-die molding machine (screw diameter
35mm, L/D=22), 150μ at molding temperature 230℃
It was molded into a thick sheet and various items were examined. Table 1 shows the results of comparison with polyethylene and propylene homopolymer alone. From this, 5 to 50% by weight of polypropylene to polyethylene,
It has been found that if it is added preferably in an amount of 10 to 40% by weight, stable molding can be achieved and molded products with even thickness can be obtained. Example 2 Example 1 for a composition in which 50% by weight of propylene homopolymer with an MFR of 3.0 g/10 minutes was added to 50% by weight of polyethylene with an MFR of 0.03, 1.0, 2.0, and 3.0.
It was made into a sheet using the same method as above, and various studies were conducted. As a result, it is desirable that the MFR of polyethylene be as low as possible; if the MFR exceeds 2.0 g/10 minutes, the sheet will sag significantly and the thickness will become noticeably uneven. The results are summarized in Table 2. Example 3 MFR0.05, 3.0, 4g/10 for 50% by weight polyethylene with density 0.954g/ cm3 at MFR2.0g/10 minutes
Propylene homopolymer at 3.0 g/10 min.Propylene-ethylene block copolymer with 15 wt.% ethylene content and crystalline propylene-ethylene random copolymer with 3.5 wt.% ethylene content at MFR3.0 g/10 min. Compositions containing 50% by weight of each polymer were formed into sheets in the same manner as in Example 1, and various studies were conducted. The results are shown in Table 3. From this, the polypropylene blended is also low.
MFR is desirable, and when MFR exceeds 3.0 g/10 minutes, the sheet sag is large and the thickness unevenness is large.
The MFR of polypropylene is limited to 3.0 g/10 minutes or less. Furthermore, similar effects were confirmed when polypropylene was used alone, as a block copolymer, or as a random copolymer.

【表】【table】

【表】【table】

【表】【table】

【表】 実施例 4 MFR0.03g/10分、密度0.940g/cm3のポリエ
チレンペレツトにMFR0.05g/10分のプロピレ
ンホモポリマーペレツトを10重量%添加した組成
物について、実施例1と同様にして成形したシー
ト、および、比較例としてこのシートを一軸延伸
装置にて面積比が原シートに対して2倍及び5倍
になるように延伸した延伸シートを得、厚みムラ
及び引裂性の評価を行なつた。 引裂性の評価は、厚みムラの評価で得られた深
絞り体の深絞り部分を切り取り、これを手で引き
裂くときの容易さにより行なつた。 結果は、表4に示したとおり、延伸シートを深
絞りしたものでは容易に引き裂かれるものであ
り、これによつて成形された深絞り容器では落下
や変形応力によつて延伸方向に裂けが発生して充
填物がもれてしまう等、実用上の点で問題のある
ものである。
[Table] Example 4 Regarding a composition in which 10% by weight of propylene homopolymer pellets with an MFR of 0.05 g/ 10 minutes were added to polyethylene pellets with an MFR of 0.03 g/10 minutes and a density of 0.940 g/cm3, Example 1 and A sheet formed in the same manner and, as a comparative example, a stretched sheet was obtained by stretching this sheet using a uniaxial stretching device so that the area ratio was 2 times and 5 times that of the original sheet. We conducted an evaluation. Tearability was evaluated by cutting out the deep-drawn portion of the deep-drawn body obtained in the evaluation of thickness unevenness and determining how easy it was to tear it by hand. As shown in Table 4, the results show that deep-drawn stretched sheets are easily torn, and deep-drawn containers formed using this method tear in the stretching direction due to falling or deformation stress. This poses problems in practical terms, such as the filling material leaking.

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 メルトフローレイト2.0g/10分以下のポリ
エチレン95〜50重量%とおよびメルトフローレイ
ト3.0g/10分以下のアイソタクチツクポリプロ
ピレン5〜50重量%とからなる樹脂組成物を常法
により延伸工程を経ることなしに成形してなるこ
とを特徴とする深絞り用オレフイン重合体シー
ト。
1. A resin composition consisting of 95-50% by weight of polyethylene with a melt flow rate of 2.0 g/10 minutes or less and 5-50% by weight of isotactic polypropylene with a melt flow rate of 3.0 g/10 minutes or less is subjected to a stretching process by a conventional method. An olefin polymer sheet for deep drawing, which is formed by forming the sheet without undergoing any process.
JP1534079A 1979-02-13 1979-02-13 Deep-drawing olefin polymer sheet Granted JPS55108433A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1534079A JPS55108433A (en) 1979-02-13 1979-02-13 Deep-drawing olefin polymer sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1534079A JPS55108433A (en) 1979-02-13 1979-02-13 Deep-drawing olefin polymer sheet

Publications (2)

Publication Number Publication Date
JPS55108433A JPS55108433A (en) 1980-08-20
JPS6236062B2 true JPS6236062B2 (en) 1987-08-05

Family

ID=11886051

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1534079A Granted JPS55108433A (en) 1979-02-13 1979-02-13 Deep-drawing olefin polymer sheet

Country Status (1)

Country Link
JP (1) JPS55108433A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5893742A (en) * 1981-12-01 1983-06-03 Showa Denko Kk Thermoforming resin composition
JPS60133039A (en) * 1983-12-21 1985-07-16 Mitsubishi Petrochem Co Ltd Thermoplastic resin composition
JPH078532B2 (en) * 1986-05-30 1995-02-01 三菱油化株式会社 Drawing method for resin sheet
AU2002362699A1 (en) 2001-10-03 2003-04-22 Atofina Research Adhesion of polyethylene on polypropylene
CN109716230B (en) 2016-09-16 2021-03-12 富士胶片株式会社 Lens Units, Camera Systems, and Lens Mounts

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5322568A (en) * 1976-08-12 1978-03-02 Sekisui Chemical Co Ltd Method of producing container
JPS5345388A (en) * 1976-10-06 1978-04-24 Asahi Chem Ind Co Ltd Multi-layer sheet
JPS593886Y2 (en) * 1977-05-30 1984-02-03 積水化学工業株式会社 food packaging containers
JPS5463996A (en) * 1977-10-28 1979-05-23 Sekisui Chem Co Ltd Thermal plastic resin film or sheet for close contact packing

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