JPH09100364A - Foamed styrene resin sheet - Google Patents
Foamed styrene resin sheetInfo
- Publication number
- JPH09100364A JPH09100364A JP7259647A JP25964795A JPH09100364A JP H09100364 A JPH09100364 A JP H09100364A JP 7259647 A JP7259647 A JP 7259647A JP 25964795 A JP25964795 A JP 25964795A JP H09100364 A JPH09100364 A JP H09100364A
- Authority
- JP
- Japan
- Prior art keywords
- sheet
- styrene resin
- molding
- container
- deep
- 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.)
- Pending
Links
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Laminated Bodies (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は2次発泡成形性に優
れたスチレン系樹脂発泡シートに関する。さらに詳しく
は、2次発泡成形時の加熱条件幅が広く、深絞り成形に
より深型容器を成形するに際して、ナキ、ヤケ等の外観
不良の発生を抑制し、成形条件幅を広くとることのでき
る、2次発泡成形性に優れたスチレン系樹脂発泡シート
に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a styrene resin foam sheet having excellent secondary foaming moldability. More specifically, the range of heating conditions at the time of secondary foam molding is wide, and when molding a deep container by deep drawing, it is possible to suppress the occurrence of appearance defects such as pear and burn and widen the range of molding conditions. The present invention relates to a styrene resin foam sheet having excellent secondary foam moldability.
【0002】[0002]
【従来の技術】スチレン系樹脂発泡シートを用いた食品
容器は、トレー、カップ、どんぶり等、様々な形で使用
されており、プラスチックのリサイクル性等、地球環境
問題に対する議論が各地でなされる現在においてもな
お、その軽量性、断熱性、耐吸湿性の高さ等により、多
くの需要を有している。2. Description of the Related Art Food containers using foamed styrene resin sheets are used in various forms such as trays, cups and bowls, and discussions on global environmental issues such as plastic recyclability are currently being held in various places. However, there is still a great demand due to its light weight, heat insulation, high resistance to moisture absorption and the like.
【0003】一般にこのスチレン系樹脂発泡シートのよ
うな熱可塑性樹脂発泡シートの2次発泡成形は、オーブ
ン等の加熱手段により発泡シートを加熱、軟化させ、そ
の直後に雌雄両金型間に導き、その後、金型で挟みつけ
るマッチモールド成形により所望の形状に成形される。
ところが、絞り比(容器高/容器口径)が1.0以上で
あるような、いわゆる深絞り成形により深型容器の成形
を行う場合には、特に容器側面部における発泡シートの
引張変形量が大きくなるため、この部分の発泡シートが
成形時に部分的に破断してしまい、これを原因とする容
器外観不良(以下、本現象を「ナキ」という)が発生し
やすくなる。In general, in the secondary foam molding of a thermoplastic resin foam sheet such as this styrene resin foam sheet, the foam sheet is heated and softened by a heating means such as an oven, and immediately after that, it is introduced between the male and female molds. After that, it is molded into a desired shape by match mold molding in which the mold is sandwiched.
However, when forming a deep-type container by so-called deep drawing, in which the drawing ratio (container height / container diameter) is 1.0 or more, the amount of tensile deformation of the foamed sheet is particularly large on the side surface of the container. Therefore, the foamed sheet in this portion is partially broken at the time of molding, and a defective appearance of the container due to this (hereinafter, this phenomenon is referred to as “Naki”) is likely to occur.
【0004】そこで、これだけの大変形を可能とするた
めに、2次発泡成形直前における加熱時の加熱温度、及
び加熱時間を大きくし、発泡シートを軟化、厚肉化させ
たうえで2次成形する方法が知られている。しかし、こ
れを行った場合、発泡シート表面のセルの破泡や樹脂の
劣化のために表層部がケロイド状になってしまう(以
下、本現象を「ヤケ」という)という問題があった。Therefore, in order to make such a large deformation possible, the heating temperature and the heating time immediately before the secondary foam molding are increased to soften and thicken the foamed sheet before the secondary molding. It is known how to do it. However, when this is done, there is a problem that the surface layer portion becomes keloid-like due to the breakage of cells on the surface of the foamed sheet and the deterioration of the resin (hereinafter, this phenomenon is referred to as “burning”).
【0005】こうした問題を解決するために、スチレン
系樹脂中にゴム分を添加した、いわゆるハイインパクト
ポリスチレンを使用したり、分子量の絶対値あるいは分
子量分布を調整することが行なわれてきた(例えば特開
昭62−22834号公報、特開平6−57028号公
報等)。ところが、このような技術は、いずれも成形後
の容器強度あるいは耐熱性が不十分であったり、コスト
高になったりと、物性良好で、かつ安価な成形容器を提
供するに至っていない。In order to solve these problems, so-called high-impact polystyrene in which a rubber component is added to a styrene resin is used, or the absolute value of the molecular weight or the molecular weight distribution has been adjusted (for example, a special method). JP-A-62-22834, JP-A-6-57028, etc.). However, none of these techniques has provided a molded container that has good physical properties and is inexpensive, such as insufficient container strength or heat resistance after molding or high cost.
【0006】[0006]
【発明が解決しようとする課題】また、前記のように、
容器成形時の発泡シートの部分的破断、およびそれによ
る容器外観不良(ナキ)を樹脂改質により防止するため
には、引張大変形に対する抗張力の高い樹脂を選定する
ことが重要である。こうした樹脂の選定は、従来、メル
トフローレートに代表される溶融せん断粘度、常温引張
強度、ビカット軟化点測定等によってなされてきた。し
かし、特に深絞り成形により深型容器を成形する際のナ
キ、ヤケといった成形不良を防止するという観点でこれ
らの評価因子のそれぞれについて検討を行ったところ、
上記成形不良の生じるものとそうでないものについて説
明することができなかった。一般にスチレン系樹脂発泡
シートの2次発泡成形時の発泡シートの表面温度は10
0〜130℃程度であるといわれており、100℃未満
ではナキが発生し、130℃を超えるとヤケが発生す
る。しかし、特に深絞り成形による深型容器の成形にお
いては、上述の通り、特に容器側面部を形成する発泡シ
ートの引張変形量が大きくなるために、ナキが発生しや
すく、成形可能な温度範囲が狭くなり、従来行われてき
たような技術を用いた場合、原反スペックの如何によっ
ては、130℃まで加熱しても、ナキが発生してしま
い、結果的に成形が不可能となってしまうことすらあっ
た。このような成形条件幅を確保するためには、従来は
単位面積あたりの発泡体重量(以下、本パラメータを
「目付」という)を上げ、発泡シートの剛性を上げるこ
とが行われてきた。しかし、こうした発泡シートの目付
アップは、すなわち容器成形コストのアップにつなが
り、好ましくない。Further, as described above,
It is important to select a resin having high tensile strength against large tensile deformation in order to prevent partial breakage of the foamed sheet at the time of molding the container and defective container appearance (naked) due to the resin modification. The selection of such a resin has heretofore been made by measuring melt shear viscosity typified by melt flow rate, tensile strength at room temperature, and Vicat softening point. However, when we examined each of these evaluation factors from the viewpoint of preventing molding defects such as pearing and burning when molding a deep container by deep drawing,
It was not possible to explain what caused the above-mentioned molding failure and what did not. Generally, the surface temperature of the foamed sheet during secondary foam molding of the styrene resin foamed sheet is 10
It is said that the temperature is about 0 to 130 ° C, and naki occurs at temperatures lower than 100 ° C, and burns occur at temperatures higher than 130 ° C. However, particularly in the molding of a deep container by deep drawing, as described above, since the amount of tensile deformation of the foamed sheet forming the side surface of the container becomes large, naki easily occurs, and the moldable temperature range is increased. When the technology becomes narrower and the conventional technique is used, depending on the specifications of the original fabric, naki may occur even if heated up to 130 ° C., resulting in impossible molding. There was even that. In order to secure such a range of molding conditions, conventionally, the foam weight per unit area (hereinafter, this parameter is referred to as "unit weight") has been increased to increase the rigidity of the foam sheet. However, increasing the basis weight of such a foamed sheet leads to an increase in the cost of forming the container, which is not preferable.
【0007】[0007]
【課題を解決するための手段】そこで、本発明者等は、
上記課題に鑑みて鋭意研究を行った結果、上記のような
スチレン系樹脂発泡シートの成形可能な温度範囲の上限
である130℃における伸長粘度特性の改良されたスチ
レン系樹脂からなる発泡シートを用いて深絞り容器成形
を行うことにより、目付アップをすることなく、工業上
十分なだけの成形条件幅を確保し、外観、物性ともに良
好な深絞り容器を得ることができることを見いだしたの
である。Means for Solving the Problems Accordingly, the present inventors have
As a result of earnest research in view of the above problems, a foamed sheet made of a styrene resin having improved extensional viscosity characteristics at 130 ° C., which is the upper limit of the temperature range in which the styrene resin foamed sheet can be molded, is used. It has been found that by performing deep drawing container molding, a deep drawing container having an industrially sufficient molding condition width can be secured and a good appearance and physical properties can be obtained without increasing the basis weight.
【0008】すなわち、130℃における伸長粘度測定
において、伸長粘度の歪硬化指数が1.5以上であるス
チレン系樹脂からなるスチレン系樹脂発泡シート、特
に、2次発泡成形の加熱直前において、密度0.2〜
0.5g/cm3 、厚み1.3〜3.0mmであるスチ
レン系樹脂発泡シートを用いて、絞り比1以上のいわゆ
る深絞り容器を成形した場合には、2次発泡成形時の加
熱条件幅が広く、上記課題が解決されることを見いだ
し、本発明を完成するに到った。更に、前記発泡シート
の片面又は両面に、非発泡フィルムを積層した積層発泡
シートとして用いてもよい。That is, in the elongational viscosity measurement at 130 ° C., a styrene resin foam sheet made of a styrene resin having a strain hardening index of elongational viscosity of 1.5 or more, particularly, a density of 0 is obtained immediately before heating in secondary foam molding. .2-
When a so-called deep-drawing container having a drawing ratio of 1 or more is formed using a styrene resin foam sheet having a thickness of 0.5 g / cm 3 and a thickness of 1.3 to 3.0 mm, heating conditions during secondary foam molding. The inventors have found that the above-mentioned problems can be solved with a wide range and completed the present invention. Further, a non-foamed film may be laminated on one side or both sides of the foamed sheet to be used as a laminated foamed sheet.
【0009】上記のような本発明に係るスチレン系樹脂
発泡シートを用いることで、特に絞り比が1.0以上の
いわゆる深絞り成形による深型容器の2次発泡成形時に
おいて、成形容器に上記ヤケ、ナキのような外観不良が
発生せず、しかも強度、断熱性等の物性の良好な成形品
を提供することが可能となった。By using the styrene-based resin foam sheet according to the present invention as described above, the above-mentioned styrenic resin foam sheet can be used as a molding container during the secondary foam molding of a deep container by so-called deep-draw molding having a drawing ratio of 1.0 or more. It has become possible to provide a molded product that does not suffer from a defective appearance such as scorch and pear and has good physical properties such as strength and heat insulation.
【0010】[0010]
【発明の実施の形態】本発明における前記スチレン系樹
脂とは、ポリスチレンが最も好適に使用されるが、スチ
レンモノマーに対して、他のビニル系単量体、例えばα
−メチルスチレン、p−メチルスチレンなどのスチレン
系モノマーや、アクリロニトリル、アクリル酸メチル、
メタクリル酸メチル、アクリル酸、メタクリル酸、無水
マレイン酸等が共重合されているものを用いてもよい。
前記他のビニル系単量体の割合はスチレンを含めた全ビ
ニル系単量体に対し0〜30重量%である。BEST MODE FOR CARRYING OUT THE INVENTION Polystyrene is most preferably used as the styrene resin in the present invention.
-Styrene monomers such as methylstyrene and p-methylstyrene, acrylonitrile, methyl acrylate,
Those in which methyl methacrylate, acrylic acid, methacrylic acid, maleic anhydride, etc. are copolymerized may be used.
The proportion of the other vinyl-based monomer is 0 to 30% by weight based on the total vinyl-based monomer including styrene.
【0011】そして、これらのスチレン系樹脂のうち、
特に、130℃における伸長粘度測定において、伸長粘
度の歪硬化指数が1.5以上となるようなスチレン系樹
脂を押出発泡等した発泡シートを用いて深絞り容器を成
形した場合、良好な2次成形性を有するのである。Of these styrene resins,
In particular, when measuring the extensional viscosity at 130 ° C., when a deep-drawing container is formed by using a foamed sheet obtained by extruding and foaming a styrene resin having a strain hardening index of the extensional viscosity of 1.5 or more, a good secondary It has moldability.
【0012】前記伸長粘度とは、メルトフローレート、
初期緩和弾性率等の、従来測定の行われてきた樹脂の溶
融粘度(=せん断粘度)とは異なり、棒状あるいは平板
状の測定サンプルの両側を、一定温度雰囲気下において
ピンチローラあるいはキャタピラにより支持した後、ピ
ンチローラあるいはキャタピラを回転させ、一定歪速度
を保つように測定サンプルに引張変形を加え、変形中の
サンプル断面積、およびピンチローラあるいはキャタピ
ラにかかるトルクを検出することにより求められるもの
である。The extensional viscosity means the melt flow rate,
Unlike the melt viscosity (= shear viscosity) of resin, which has been conventionally measured such as initial relaxation elastic modulus, both sides of a rod-shaped or plate-shaped measurement sample were supported by pinch rollers or tracks under a constant temperature atmosphere. After that, the pinch roller or caterpillar is rotated, tensile deformation is applied to the measurement sample so as to maintain a constant strain rate, and the sample cross-sectional area during deformation and the torque applied to the pinch roller or caterpillar are detected. .
【0013】通常、前記伸長粘度測定中における検出ト
ルクは、歪量の増大とともにサンプル断面積が急激に減
少するために、測定初期にピークを形成した後、なだら
かに減少する。ところが、樹脂によっては、この検出ト
ルクのピークが2山となり、その結果、高歪領域におけ
る伸長粘度が急激に上昇する、いわゆる歪硬化性を有す
るものがある。この歪硬化性の度合いを表すパラメータ
として、歪硬化指数(the viscosity growth function)
が知られている(Bradley and Phillips, ANTEC'90,71
7)。Usually, the detected torque during the measurement of the extensional viscosity decreases gently after the peak is formed at the initial stage of measurement because the sample cross-sectional area sharply decreases as the amount of strain increases. However, some resins have a so-called strain hardening property in which the peak of the detected torque has two peaks, and as a result, the extensional viscosity in the high strain region rapidly increases. The parameter indicating the degree of strain hardening is the strain growth index.
Is known (Bradley and Phillips, ANTEC'90,71
7).
【0014】つまり、この伸長粘度の歪硬化指数とは、
一定歪速度(=ε)における1軸伸長粘度測定におい
て、下記式(1)That is, the strain hardening index of this extensional viscosity is
In the uniaxial elongational viscosity measurement at a constant strain rate (= ε), the following formula (1)
【0015】[0015]
【数1】 (Equation 1)
【0016】により定義されるηe + である。ここで、
F(t)は検出トルク、A0 はサンプルの初期断面積、
tは時間である。歪硬化性のない樹脂の場合、伸長粘度
(対数)を時間(対数)に対してプロットした場合、伸
長粘度ηe はゼロせん断粘度の3倍に漸近する曲線とな
り、この場合、歪硬化指数ηe + は1となる。歪硬化性
を有する樹脂の場合、該プロットが漸近曲線とはなら
ず、特に高歪領域においてηe が急激に立ち上がり、ピ
ークを形成した後、破断する。本発明においては、歪硬
化性を有する樹脂のピーク時のηe と、同一歪(時間)
における歪硬化性のない樹脂のηe との比として歪硬化
指数ηe + を定義する。Η e + defined by here,
F (t) is the detected torque, A 0 is the initial cross-sectional area of the sample,
t is time. When the elongational viscosity (logarithm) is plotted against time (logarithm) in the case of a resin having no strain-hardening property, the elongational viscosity η e becomes a curve asymptotic to 3 times the zero-shear viscosity. e + becomes 1. In the case of a resin having a strain hardening property, the plot does not become an asymptotic curve, and η e rises sharply in a particularly high strain region to form a peak and then break. In the present invention, the same strain (time) as η e at the peak of the resin having strain hardening property
The strain hardening index η e + is defined as the ratio with respect to η e of the resin having no strain hardening property.
【0017】本発明では、スチレン系樹脂のうち、13
0℃における伸長粘度測定において、伸長粘度の歪硬化
指数ηe + が1.5以上であるスチレン系樹脂を用い
る。この粘度の歪硬化指数が1.5以上のスチレン系樹
脂は、例えば、特開平6−57028号公報、特開平6
−256420号公報等に記載されたようなスチレン系
樹脂のうちから、前記した伸長粘度測定において歪硬化
指数が1.5以上のものを選択して用いることができ
る。本発明に係る発泡シートは、このような歪硬化指数
を有するスチレン系樹脂に対し、タルクやインジゴ、炭
酸カルシウム、高級脂肪酸金属塩(ステアリン酸バリウ
ム、ステアリン酸マグネシウム、ステアリン酸亜鉛等)
等の気泡調整剤、流動パラフィン等の成形性調整剤等を
適宜添加し、押出機を用いて溶融、混合し、発泡剤を圧
入した後、円筒形状、平板形状等のダイより押出発泡さ
せてシート化することにより製造される。In the present invention, 13 of the styrene resins are used.
In measurement of elongational viscosity at 0 ° C., a styrene resin having a strain hardening index η e + of elongational viscosity of 1.5 or more is used. Styrenic resins having a strain hardening index of 1.5 or more of this viscosity are disclosed in, for example, JP-A-6-57028 and JP-A-6-57028.
Among the styrene-based resins described in JP-A-256420, those having a strain hardening index of 1.5 or more in the above-mentioned elongational viscosity measurement can be selected and used. The foamed sheet according to the present invention has talc, indigo, calcium carbonate, higher fatty acid metal salts (barium stearate, magnesium stearate, zinc stearate, etc.) against styrene resins having such a strain hardening index.
Etc., a foam regulator such as liquid paraffin, and a moldability regulator such as liquid paraffin are appropriately added, melted and mixed by using an extruder, and a foaming agent is press-fitted, and then extruded and foamed from a die having a cylindrical shape, a flat plate shape or the like. It is manufactured by forming a sheet.
【0018】上記スチレン系樹脂発泡シートは、これを
単体で用いてもよく、また、該発泡シートの少なくとも
片面に、上記スチレン系樹脂の他、エチレン−ビニルア
ルコール共重合体、エチレン−酢酸ビニル共重合体、ポ
リ塩化ビニリデン、ポリプロピレン、ポリエチレン、ポ
リブタジエン、ポリイソプレン等の非発泡フィルムを積
層してなる積層シートとして用いてもよい。これらの非
発泡樹脂フィルムは、成形容器の形状、要求物性(強
度、耐熱性等)により適宜決められるが、特に深絞り成
形により深型容器を成形するに際しては、スチレン系樹
脂の他、エチレン−ビニルアルコール共重合体、ポリプ
ロピレンが特に好適に使用される。The styrenic resin foam sheet may be used alone, and in addition to the styrene resin, an ethylene-vinyl alcohol copolymer, an ethylene-vinyl acetate copolymer may be used on at least one surface of the foam sheet. It may be used as a laminated sheet formed by laminating non-foamed films of a polymer, polyvinylidene chloride, polypropylene, polyethylene, polybutadiene, polyisoprene and the like. These non-foamed resin films are appropriately determined depending on the shape of the molding container and the required physical properties (strength, heat resistance, etc.). Especially when molding a deep container by deep drawing, in addition to the styrene resin, ethylene- Vinyl alcohol copolymer and polypropylene are particularly preferably used.
【0019】また、上記スチレン系樹脂発泡シートを、
特に深絞り成形に供する際には、発泡シートの密度は
0.2〜0.5g/cm3 、厚み1.3〜3.0mmと
することが好適である。密度が0.2g/cm3 未満で
は、深絞り容器成形時の発泡体強度が不足し、実質上成
形条件幅がなくなってしまうために好ましくなく、0.
5g/cm3 を超えた場合には、コストアップの他、発
泡容器の特徴である軽量性および断熱性が低下するため
好ましくない。また、厚み1.3mm未満では、得られ
る深絞り容器の厚みが薄すぎ、断熱性が不十分となり、
3.0mmを超える場合には、成形条件幅が狭くなるた
め好ましくない。In addition, the styrene resin foam sheet,
Particularly when subjected to deep drawing, it is preferable that the density of the foamed sheet is 0.2 to 0.5 g / cm 3 and the thickness is 1.3 to 3.0 mm. When the density is less than 0.2 g / cm 3 , the foam strength at the time of molding a deep-drawing container is insufficient and the molding condition width is substantially lost, which is not preferable.
If it exceeds 5 g / cm 3 , not only is the cost increased, but the lightness and heat insulating properties of the foam container are also reduced, which is not preferable. On the other hand, if the thickness is less than 1.3 mm, the thickness of the obtained deep-drawn container is too thin, and the heat insulation becomes insufficient,
If it exceeds 3.0 mm, the molding condition width becomes narrow, which is not preferable.
【0020】[0020]
【実施例】以下、実施例、及び比較例を挙げて本発明を
具体的に述べるが、本発明はこれらの実施例のみに限定
されるものではない。EXAMPLES The present invention will be specifically described below with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.
【0021】(実施例1〜6、比較例1〜4)第1表に
示すような130℃における歪硬化指数、メルトフロー
レート、ビカット軟化点を有する4種類のスチレン系樹
脂を用いて、常法により押出発泡して作製した発泡シー
トを発泡層として用い、第2表の実施例1〜6及び比較
例1〜4に示す構成、密度、厚みの発泡シートを作製し
た。なお、前記発泡シートの発泡層を構成するスチレン
系樹脂の歪硬化指数は、東洋精機製作所製伸長粘度計
「メルテンレオメータ」を用いて行った130℃の伸長
粘度の測定結果から、前記式(1)により求めた。前記
伸長粘度測定の際、棒状サンプル(φ5〜7mm)は1
30(±0.3)℃に調整されたシリコーンオイル中で
約10分間加熱し、また歪速度は0.01〔s-1〕とし
た。(Examples 1 to 6 and Comparative Examples 1 to 4) Four kinds of styrene resins having a strain hardening index at 130 ° C., a melt flow rate and a Vicat softening point as shown in Table 1 were used, and Using the foamed sheet produced by extrusion foaming by the method as a foaming layer, a foamed sheet having a structure, density and thickness shown in Examples 1 to 6 and Comparative Examples 1 to 4 in Table 2 was produced. The strain hardening index of the styrene-based resin forming the foamed layer of the foamed sheet is calculated by the above formula (from the measurement result of the elongational viscosity at 130 ° C. using the elongational viscometer “Melten Rheometer” manufactured by Toyo Seiki Seisakusho Ltd.). It was determined by 1). When measuring the extensional viscosity, the rod-shaped sample (φ5 to 7 mm) is 1
It was heated in silicone oil adjusted to 30 (± 0.3) ° C. for about 10 minutes, and the strain rate was set to 0.01 [s −1 ].
【0022】[0022]
【表1】 [Table 1]
【0023】[0023]
【表2】 [Table 2]
【0024】次に、これら発泡シートの深絞り成形によ
り、容器高=105mm、容器口径=96mm、絞り比
1.1の深型容器の成形を行った結果、得られた成形品
の外観検査結果、および2次発泡成形の際の成形直前の
発泡シートの表面温度を赤外線温度計により測定した結
果を、第2表に併せて示す。Next, by deep drawing of these foamed sheets, a deep container having a container height of 105 mm, a container diameter of 96 mm and a drawing ratio of 1.1 was formed. As a result, the appearance of the obtained molded product was inspected. Table 2 also shows the results of measuring the surface temperature of the foamed sheet immediately before molding in the secondary foam molding by an infrared thermometer.
【0025】[0025]
【発明の効果】以上のように、本発明に係るスチレン系
樹脂発泡シートは、2次発泡成形時の加熱温度幅が広
く、ナキ、ヤケ等の外観不良を発生することなく深絞り
成形による深型容器の成形が可能である。INDUSTRIAL APPLICABILITY As described above, the styrene resin foam sheet according to the present invention has a wide heating temperature range at the time of secondary foam molding and can be deep-drawn by deep drawing without causing defective appearance such as pear and burn. Molded containers can be molded.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 // B29K 25:00 105:04 B29L 9:00 C08L 25:00 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 6 Identification number Office reference number FI technical display location // B29K 25:00 105: 04 B29L 9:00 C08L 25:00
Claims (4)
て、伸長粘度の歪硬化指数が1.5以上であるスチレン
系樹脂からなる、深絞り成形に適したスチレン系樹脂発
泡シート。1. A styrene-based resin foam sheet suitable for deep drawing, comprising a styrene-based resin having a strain-hardening index of elongation viscosity of 1.5 or more in elongation viscosity measurement at 130 ° C.
2〜0.5g/cm 3 、厚みが1.3〜3.0mmであ
ることを特徴とする請求項1記載のスチレン系樹脂発泡
シート。2. The styrene resin foam sheet has a density of 0.
2 to 0.5 g / cm Three, The thickness is 1.3 to 3.0 mm
Styrenic resin foam according to claim 1, characterized in that
Sheet.
レン系樹脂発泡シートの片面又は両面に非発泡樹脂フィ
ルムを積層してなる積層発泡シート。3. A laminated foam sheet obtained by laminating a non-foamed resin film on one side or both sides of the styrene resin foamed sheet according to claim 1 or 2.
れた発泡シートを深絞り成形してなる深型容器。4. A deep container formed by deep-drawing the foam sheet according to any one of claims 1 to 3.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7259647A JPH09100364A (en) | 1995-10-06 | 1995-10-06 | Foamed styrene resin sheet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7259647A JPH09100364A (en) | 1995-10-06 | 1995-10-06 | Foamed styrene resin sheet |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH09100364A true JPH09100364A (en) | 1997-04-15 |
Family
ID=17336961
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7259647A Pending JPH09100364A (en) | 1995-10-06 | 1995-10-06 | Foamed styrene resin sheet |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH09100364A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001354718A (en) * | 2000-06-14 | 2001-12-25 | Idemitsu Petrochem Co Ltd | Styrene resin and molded product thereof |
-
1995
- 1995-10-06 JP JP7259647A patent/JPH09100364A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001354718A (en) * | 2000-06-14 | 2001-12-25 | Idemitsu Petrochem Co Ltd | Styrene resin and molded product thereof |
JP4681103B2 (en) * | 2000-06-14 | 2011-05-11 | 出光興産株式会社 | Styrenic resin and molded products thereof |
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