JPS6331957Y2 - - Google Patents

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Publication number
JPS6331957Y2
JPS6331957Y2 JP1983119606U JP11960683U JPS6331957Y2 JP S6331957 Y2 JPS6331957 Y2 JP S6331957Y2 JP 1983119606 U JP1983119606 U JP 1983119606U JP 11960683 U JP11960683 U JP 11960683U JP S6331957 Y2 JPS6331957 Y2 JP S6331957Y2
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JP
Japan
Prior art keywords
resin
film
glass transition
resin film
container
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
JP1983119606U
Other languages
Japanese (ja)
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JPS6026835U (en
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Filing date
Publication date
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Priority to JP11960683U priority Critical patent/JPS6026835U/en
Publication of JPS6026835U publication Critical patent/JPS6026835U/en
Application granted granted Critical
Publication of JPS6331957Y2 publication Critical patent/JPS6331957Y2/ja
Granted legal-status Critical Current

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  • Laminated Bodies (AREA)
  • Containers Having Bodies Formed In One Piece (AREA)

Description

【考案の詳細な説明】 本考案は、合成樹脂発泡シートを主材とする食
品容器、特に電子レンジでそのまま加熱調理する
のに好適な食品容器に関する。
[Detailed Description of the Invention] The present invention relates to a food container whose main material is a synthetic resin foam sheet, and particularly to a food container suitable for heating and cooking in a microwave oven.

最近、電子レンジでそのまま加熱調理(加温処
理も含む)できる食品収納容器が種々の食品につ
いての包装容器として市場に供されている。この
ような食品容器について通常望まれる性能は、 (イ) 食品収納状態で加熱しても実質的に寸法変化
や変形を生じない耐熱性を有すること。
BACKGROUND ART Recently, food storage containers that can be directly cooked (including heating treatment) in a microwave oven have been put on the market as packaging containers for various foods. The performances normally desired for such food containers are: (a) heat resistance that does not substantially cause dimensional changes or deformation even when heated while storing food;

(ロ) 食品収納状態で片端を持つて保持できる程度
の剛性を有すること。
(b) It must have enough rigidity to be held by holding one end while storing food.

(ハ) 加熱調理後、直接手で持てる程度の断熱性を
有すること。
(c) It must have enough insulation to be able to be held directly in the hand after cooking.

(ニ) いつたん加熱したら収納食品の保温性がよい
こと。
(d) Stored food retains heat well once heated.

(ホ) 耐水性、耐油性を有すること。(e) Must be water and oil resistant.

(ヘ) 食品衛生上問題のないこと。(f) There should be no food hygiene problems.

(ト) 外観上好ましい印象を与えること。(g) Give a favorable impression in terms of appearance.

等である。etc.

従来より、加熱調理可能な食品収納容器として
は、紙とポリエステル樹脂との複合材料からなる
容器が用いられているが、この容器は、上記イ,
ロ,ハおよびニの点で充分満足できるものではな
く、例えば電子レンジでの加熱時にラツプフイル
ムの収縮力あるいは水蒸気圧に抗しきれず変形を
起したり、加熱調理直後に手で持つた場合に熱く
取扱い難い、加温した食品が冷え易い、といつた
欠点を有していた。その上、前記容器は基材が紙
であるため、その製造において容器状とするには
コーナー部分を重ね合せる必要があり、殊に剛性
の高い厚肉の容器や深絞り容器あるいは複雑な形
状の容器の製造が困難であるという問題点があつ
た。
Conventionally, containers made of a composite material of paper and polyester resin have been used as food storage containers that can be heated and cooked.
It is not completely satisfactory in points B, C, and D. For example, when heated in a microwave oven, the wrap film may become deformed due to its shrinkage force or water vapor pressure, or it may become hot when held in the hand immediately after cooking. It had drawbacks such as being difficult to handle and allowing heated food to cool easily. Furthermore, since the base material of the container is paper, it is necessary to overlap the corner portions in order to make it into a container shape during manufacturing. There was a problem in that the container was difficult to manufacture.

そこで、本考案者らは、直接加熱調理できる食
品容器として、調理直後に手で持つても熱く感じ
ずかつ保形性もある容器の開発を試み、一般に断
熱性が良い素材として知られている合成樹脂発泡
体を使用せんとして検討を行なつた。従来より、
ポリスチレン系樹脂発泡シート等の合成樹脂発泡
体は容器その他の種々の用途に利用されている
が、これを電子レンジで直接加熱調理ができる食
品としては市場に供されたものはない。これは、
特にカツプラーメン等の容器に多用されているポ
リスチレン系樹脂の発泡体等では、耐熱性が充分
でなく、常温での剛性および保形性は問題ないも
のの、加熱されると剛性が著しく低下して変形し
易くなり、あるいは高温時の耐油性が必ずしも十
分でなく、100℃前後あるいはそれ以上の温度に
もなる電子レンジでの加熱調理用の容器としては
適さず、また他の耐熱性の良い発泡体の場合コス
トが高くかつ容器形状への成形加工が容易でない
といつた問題があるからである。
Therefore, the inventors of the present invention attempted to develop a food container that can be heated and cooked directly, and which does not feel hot even when held in the hand immediately after cooking, and which retains its shape. A study was conducted assuming that synthetic resin foam was not used. Traditionally,
Synthetic resin foams such as polystyrene resin foam sheets are used for various purposes such as containers, but there is no food product on the market that can be directly heated in a microwave oven. this is,
In particular, polystyrene resin foams, etc., which are often used in containers such as cutlet ramen, do not have sufficient heat resistance, and although there are no problems with rigidity and shape retention at room temperature, the rigidity decreases significantly when heated. It becomes easily deformed, does not necessarily have sufficient oil resistance at high temperatures, and is not suitable as a container for cooking in a microwave oven, which can reach temperatures around 100℃ or higher, and other foams with good heat resistance are not suitable. This is because, in the case of containers, there are problems such as high cost and difficulty in molding them into container shapes.

本考案者らは、上記に鑑みてさらに研究、検討
を重ねた結果、ポリフエニレンエーテル系樹脂と
ポリスチレン系樹脂との混合樹脂の発泡シート
が、剛性および耐熱性があつて加熱したときの剛
性に優れており、特にこの発泡シートにガラス転
移点の高い熱可塑性樹脂フイルムを積層すれば、
加熱時の剛性および保形性をさらに高め得るとと
もに成形加工性その他の属性も改善でき、電子レ
ンジで直接加熱調理できる食品容器としてきわめ
て好適に利用できることを知見し、本考案はこの
知見に基いてなしたものである。
In view of the above, the inventors of the present invention have conducted further research and consideration, and have found that a foamed sheet made of a mixed resin of polyphenylene ether resin and polystyrene resin has high rigidity and heat resistance, and has high rigidity when heated. In particular, if a thermoplastic resin film with a high glass transition temperature is laminated on this foam sheet,
It was discovered that the rigidity and shape retention during heating can be further enhanced, and the moldability and other attributes can also be improved, making it extremely suitable for use as a food container that can be heated and cooked directly in a microwave oven.The present invention is based on this knowledge. This is what was done.

すなわち、本考案は、ポリフエニレンエーテル
系樹脂10〜50重量%とポリスチレン系樹脂90〜50
重量%との混合樹脂を素材とする発泡倍率3〜80
倍、厚み1〜6mmの発泡シートの少なくとも片面
に、ガラス転移点が100℃以上の熱可塑性樹脂フ
イルムまたは同フイルムを含む合成樹脂の複層フ
イルムを積層した複合シートから一体に成形され
てなる食品容器を要旨とするものである。
That is, the present invention uses 10 to 50% by weight of polyphenylene ether resin and 90 to 50% by weight of polystyrene resin.
Foaming ratio 3 to 80 made from resin mixed with weight%
A food product that is integrally formed from a composite sheet made by laminating a thermoplastic resin film with a glass transition point of 100°C or higher, or a multilayer synthetic resin film containing the same film, on at least one side of a foamed sheet with a thickness of 1 to 6 mm. The gist is the container.

次に本考案の実施例を図面に基いて説明する。
図において、Aは本考案に係る食品容器を示し、
ポリフエニレンエーテル系樹脂とポリスチレン系
樹脂との混合樹脂を押出し発泡成形して得られた
発泡シート1の少なくとも片面に、ガラス転移点
が100℃以上の熱可塑性樹脂フイルム2または同
フイルム2を含む合成樹脂の複層フイルムを積層
した複合シートを素材とし、これをプレス成形、
真空成形等の適宜の成形手段により第1図あるい
は第3図、第4図その他の所望の容器形状に一体
に成形してなる。
Next, embodiments of the present invention will be described based on the drawings.
In the figure, A indicates a food container according to the present invention,
At least one side of a foamed sheet 1 obtained by extruding and foam-molding a mixed resin of a polyphenylene ether resin and a polystyrene resin contains a thermoplastic resin film 2 having a glass transition point of 100° C. or higher, or the same film 2. The material is a composite sheet made by laminating multiple layers of synthetic resin films, and this is press-molded.
It is integrally molded into a desired container shape as shown in FIG. 1, FIG. 3, FIG.

上記の発泡シート1の素材である混合樹脂はポ
リフエニレンエーテル系樹脂とポリスチレン系樹
脂とからなるものであるが、その一方のポリフエ
ニレンエーテル系樹脂としては、ポリ(2,6−
ジメチルフエニレン−1,4−エーテル)、ポリ
(2,6−ジエチルフエニレン−1,4−エーテ
ル)等の当該分野で公知のフエニレンエーテル系
樹脂を使用でき、スチレン系化合物を共重合させ
たものも使用できる。他方、ポリスチレン系樹脂
としてはポリスチレン樹脂のほか、スチレンと無
水マイレン酸との共重合樹脂その他のスチレンを
主体とする共重合体およびAS樹脂やABS樹脂等
を用いることができる。また前記混合樹脂にタル
ク等の無機質フイラーを添加混合した樹脂を用い
ることもできる。この発泡シートの表皮層の発泡
倍数を小さくしたり、あるいは殆んど発泡してい
ないスキン層を形成するのが好ましい。
The mixed resin that is the material of the foamed sheet 1 is composed of polyphenylene ether resin and polystyrene resin, and one of the polyphenylene ether resins is poly(2,6-
Phenylene ether resins known in the art such as dimethylphenylene-1,4-ether) and poly(2,6-diethylphenylene-1,4-ether) can be used, and styrene compounds can be copolymerized. You can also use On the other hand, as the polystyrene resin, in addition to polystyrene resin, a copolymer resin of styrene and maleic anhydride, other styrene-based copolymers, AS resin, ABS resin, etc. can be used. Further, a resin obtained by adding and mixing an inorganic filler such as talc to the above-mentioned mixed resin can also be used. It is preferable to reduce the foaming ratio of the skin layer of this foamed sheet, or to form a skin layer that is hardly foamed.

上記の混合樹脂はポリフエニレンエーテル系樹
脂10〜50重量%、ポリスチレン系樹脂90〜50重量
%の混合比率にすることが必要である。すなわち
ポリフエニレンエーテル系樹脂が混合樹脂中の50
重量%を越えると、得られた発泡シートの耐熱性
および剛性は向上するが、シート成形性が不良で
所望の容器状に成形し難く、また10重量%末満で
はシート成形性は良好であるが、得られた容器の
耐熱性および剛性が不充分で、電子レンジでの加
熱調理後の取扱いに難があり好ましくない。な
お、この混合樹脂中には必要に応じて公知の各種
添加剤を含有する。
The above mixed resin needs to have a mixing ratio of 10 to 50% by weight of polyphenylene ether resin and 90 to 50% by weight of polystyrene resin. In other words, polyphenylene ether resin is 50% of the mixed resin.
If it exceeds 10% by weight, the heat resistance and rigidity of the obtained foamed sheet will improve, but the sheet formability will be poor and it will be difficult to form it into the desired container shape, and if it is less than 10% by weight, the sheet formability will be good. However, the resulting container has insufficient heat resistance and rigidity, making it difficult to handle after cooking in a microwave oven, which is undesirable. In addition, this mixed resin contains various known additives as necessary.

また、上記発泡シート1は、発泡倍率3〜80倍
で、厚み1〜6mmとすることが必要である。すな
わち、発泡倍率が80倍を越えると、厚みを6mmと
しかつ積層フイルム層の厚みを比較的厚くした場
合にも剛性が不充分となり、食品収納状態で片端
を持つて保持した際あるいは加熱した際に変形が
生じ易く、また3倍未満では断熱性が不充分で加
熱調理後の取り扱いが従来の紙−ポリエステル容
器と殆んど変らないことになり不適当である。さ
らに厚みが6mmを越えると、熱成形性が悪くなり
容器形状への成形加工が困難となり、また1mm未
満の場合にはやはり断熱性および保形性の点で不
適当である。このような発泡倍率や厚みは押出し
発泡成形の条件を変えることによつて設定でき
る。
Further, the foamed sheet 1 needs to have a foaming ratio of 3 to 80 times and a thickness of 1 to 6 mm. In other words, if the expansion ratio exceeds 80 times, even if the thickness is 6 mm and the thickness of the laminated film layer is relatively thick, the rigidity will be insufficient, and when holding food by holding one end while storing it or heating it. deformation is likely to occur, and if the container is less than 3 times as large, the heat insulation properties will be insufficient and the handling after cooking will be almost the same as that of conventional paper-polyester containers, which is unsuitable. Further, if the thickness exceeds 6 mm, thermoformability deteriorates and it becomes difficult to mold into a container shape, and if the thickness is less than 1 mm, it is still unsuitable in terms of heat insulation and shape retention. Such expansion ratio and thickness can be set by changing the extrusion foam molding conditions.

上記の発泡シート1に積層するガラス転移点
100℃以上の熱可塑性樹脂フイルム2としては、
ポリカーボネートのほか、ポリフエニレンオキサ
イド、ポリサルフオン、高重度ポリスチレン、ポ
リメチルメタクリレート、ポリアクリロニトリ
ル、ポリメタクリロニトリル、ポリビニルホルマ
ール、セルロースアセテート、セルロースブチレ
ート、ポリ−p−ビニルベンジルアルコール、ポ
リビニルピロリドン、ポリ−α−メチルスチレ
ン、ポリ−tert−ブチルスチレン等の熱可塑性樹
脂を例示でき、中でもガラス転移点105℃以上の
ものが好適に用いられる。特に前記ポリカーボネ
ートには様々のものがあるが、そのうちガラス転
移点100℃以上のものは芳香族ポリカーボネート
又は芳香族を含むポリカーボネートの中に多数あ
り、その中から適当に選択できる。4,4′−ジオ
キシジフエニール−2,2′プロパンポリカーボネ
ートはその一つであり、非常に好ましいものであ
る。
Glass transition point laminated to the above foam sheet 1
As the thermoplastic resin film 2 at 100℃ or higher,
In addition to polycarbonate, polyphenylene oxide, polysulfone, high-density polystyrene, polymethyl methacrylate, polyacrylonitrile, polymethacrylonitrile, polyvinyl formal, cellulose acetate, cellulose butyrate, poly-p-vinylbenzyl alcohol, polyvinylpyrrolidone, poly- Examples include thermoplastic resins such as α-methylstyrene and poly-tert-butylstyrene, among which those with a glass transition point of 105° C. or higher are preferably used. In particular, there are various types of polycarbonates, among which many aromatic polycarbonates or aromatic-containing polycarbonates have a glass transition point of 100° C. or higher, and the polycarbonate can be appropriately selected from among them. 4,4'-dioxydiphenyl-2,2'propane polycarbonate is one of them and is highly preferred.

なお、ガラス転移点はガラス転移の起こる温度
であつて、熱可塑性樹脂等の物質はガラス転移点
以下では分子および分子セグメントの運動が凍結
された状態であり、従つて極めて剛性の高い状態
に保持され、またこのガラス転移点は樹脂の種類
によつては一義的には決まらず、重合度、分子構
造、分子形態や共重合成分等によつて変わる。
The glass transition point is the temperature at which glass transition occurs, and below the glass transition point of materials such as thermoplastic resins, the motion of molecules and molecular segments is frozen, and therefore they remain in an extremely rigid state. Furthermore, this glass transition point is not uniquely determined by the type of resin, but varies depending on the degree of polymerization, molecular structure, molecular form, copolymerization components, etc.

ガラス転移点の測定方法としては、種々の方法
があるが、ここでは示差熱分析(DTA)にて行
ない、鮮明なデータが得られない場合は熱機械的
分析(TMA)を補助的に併用するものとし、い
ずれも昇温速度は5℃/分とする。また樹脂の混
合が行なわれ、完全にアロイ化している場合は混
合品のガラス転移点とし、また混練が不十分で複
数の転移点がある場合は成分樹脂のガラス転移点
の成分重量比による加重平均とする。
There are various methods for measuring the glass transition point, but here we will use differential thermal analysis (DTA), and if clear data cannot be obtained, thermomechanical analysis (TMA) will also be used as a supplement. In both cases, the temperature increase rate is 5°C/min. In addition, if the resins are mixed and completely alloyed, the glass transition point of the mixed product is taken as the glass transition point, and if there are multiple transition points due to insufficient kneading, the glass transition point of the component resin is weighted by the component weight ratio. Take the average.

この熱可塑性樹脂フイルム2は、第1図または
第2図に示すように、これを単層で上記発泡シー
ト1の片面もしくは両面に積層して食品容器Aの
構成素材である複合シートとして実施するほか、
第5図または第6図に示すように前記熱可塑性樹
脂フイルム2と他の樹脂フイルム層3との複層フ
イルム4とし、該複層フイルム4を発泡シート1
に積層して実施することもできる。食品容器とし
ての耐油性やガスバリヤー性等をさらに改善する
ということから、前記樹脂フイルム層3として、
ポリエチレンやポリプロピレン等のポリオレフイ
ン系樹脂、ポリエステル系樹脂、ポリ塩化ビニリ
デン系樹脂、ポリアミド系樹脂等の比較的耐油性
やガスバリヤー性(水分や蒸気に対するバリヤー
性も含む)等のよい合成樹脂のフイルムを用い、
該樹脂フイルム層3が表面層となるように発泡シ
ートの片面(第5図)もしくは両面(第6図)に
積層するのが好ましく、特に前記積層が発泡シー
ト片面である場合、第5図のように前記樹脂フイ
ルム層3を容器内面側に向けて成形するのが好ま
しい。また熱可塑性樹脂フイルム2を単層で発泡
シートに積層した場合にも、表面層として少なく
とも容器内面側に前記樹脂フイルム層3と同様の
合成樹脂をフイルム積層またはコーテイングして
おくのが望ましい。このように少なくとも容器内
側表面層として耐油性やガスバリヤー性のよい樹
脂フイルム層が設けられていると、加熱時に生じ
る食用油等による悪影響を防止できかつ収納され
た食品の保存性を一層高めることができる。
As shown in FIG. 1 or 2, this thermoplastic resin film 2 is laminated as a single layer on one or both sides of the foamed sheet 1 to form a composite sheet that is a constituent material of the food container A. others,
As shown in FIG. 5 or 6, a multilayer film 4 is formed by the thermoplastic resin film 2 and another resin film layer 3, and the multilayer film 4 is formed into a foamed sheet 1.
It can also be carried out by laminating them. In order to further improve oil resistance, gas barrier properties, etc. as a food container, as the resin film layer 3,
We use synthetic resin films with relatively good oil resistance and gas barrier properties (including moisture and vapor barrier properties) such as polyolefin resins such as polyethylene and polypropylene, polyester resins, polyvinylidene chloride resins, and polyamide resins. use,
It is preferable that the resin film layer 3 is laminated on one side (FIG. 5) or both sides (FIG. 6) of the foam sheet so as to serve as a surface layer. In particular, when the lamination is on one side of the foam sheet, the resin film layer 3 shown in FIG. It is preferable to mold the resin film layer 3 toward the inner surface of the container. Even when the thermoplastic resin film 2 is laminated in a single layer on a foamed sheet, it is desirable to laminate or coat at least the inner surface of the container with a synthetic resin similar to the resin film layer 3 as a surface layer. In this way, if a resin film layer with good oil resistance and gas barrier properties is provided at least as the inner surface layer of the container, it is possible to prevent the harmful effects of cooking oil, etc. that occur during heating, and further enhance the preservation of the stored food. I can do it.

上記発泡シート1と熱可塑性樹脂フイルム2お
よび熱可塑性樹脂フイルム2と樹脂フイルム層3
のいずれの積層の場合にも、中間層を介しないで
熱融着する方法と接着のための中間層を介する方
法とがある。前記の中間層としては、一層の場合
と、種類の異なる複数層の場合があり、またこれ
らは熱融着可能な熱可塑性樹脂フイルムの場合も
あるし、普通一般に接着剤と呼ばれる素材の場合
もあり、それぞれ単独に用いても、両者を併用し
てもよい。ただし、揮発成分を含有するような接
着剤の場合は塗布乾燥後ドライラミネーシヨン
(熱融着)できるようなものが好ましい。又揮発
成分を含まぬ硬化型のものも好ましい。具体例と
して、接着剤としてはアクリル樹脂系、ウレタン
樹脂系等が用いられる。また熱融着フイルムとし
てはエチレン酢酸ビニル共重合樹脂、ポリスチレ
ン系樹脂等が適当である。なお接着をより強固に
するためにアンカーコート剤と称されるものの使
用が好ましいこともある。
The foamed sheet 1 and the thermoplastic resin film 2 and the thermoplastic resin film 2 and the resin film layer 3
In any case of lamination, there are two methods: heat-sealing without an intermediate layer and methods using an intermediate layer for adhesion. The intermediate layer may be a single layer or multiple layers of different types, and may be a heat-sealable thermoplastic resin film or a material commonly called an adhesive. Each of these may be used alone or both may be used in combination. However, in the case of adhesives containing volatile components, it is preferable to use adhesives that can be dry laminated (heat fused) after application and drying. A curable type containing no volatile components is also preferred. As a specific example, an acrylic resin type adhesive, a urethane resin type adhesive, or the like is used as the adhesive. Further, as the heat-fusion film, ethylene vinyl acetate copolymer resin, polystyrene resin, etc. are suitable. Note that in order to make the adhesion stronger, it may be preferable to use what is called an anchor coating agent.

また上記熱可塑性樹脂フイルム2の厚みは30〜
500ミクロンとするのが好適であり、この厚みが
薄すぎるとフイルムを積層した効果、すなわち剛
性保持効果、特に加熱したときの剛性保持効果が
低下することになり、厚すぎると容器自体が重く
なるとともにコスト高となり好ましくない。さら
に前記のフイルム2と併用する他の樹脂フイルム
層3の厚みは5〜200ミクロン程度が好適で、複
層フイルム4全体としての厚みは35〜550ミクロ
ン程度に設定するのが望ましく、あまり厚くなり
すぎるとやはり重くかつコスト高となり好ましく
ない。
In addition, the thickness of the thermoplastic resin film 2 is 30~
The preferred thickness is 500 microns; if this thickness is too thin, the effect of laminating the films, that is, the rigidity retention effect, especially when heated, will be reduced, and if it is too thick, the container itself will become heavy. This also increases costs, which is undesirable. Furthermore, the thickness of the other resin film layer 3 used together with the film 2 is preferably about 5 to 200 microns, and the thickness of the multilayer film 4 as a whole is preferably set to about 35 to 550 microns, so that it is not too thick. If it is too large, it becomes heavy and costly, which is not preferable.

上記のように本考案の食品容器は、その構成主
体である発泡シート1がポリフエニレンエーテル
系樹脂とポリスチレン系樹脂との混合樹脂からな
るもので、これ自体が剛性および耐熱性良好で加
熱したときにもかなりの剛性を保持できる上、特
にこの発泡シート1の片面にガラス転移点が100
℃以上の熱可塑性樹脂フイルム2または同フイル
ム2を含む合成樹脂の複層フイルムを積層してあ
るので、電子レンジで直接加熱調理する食品容器
としての使用上重要な要素を占める剛性および保
形性がさらに改善され、加熱したときにも充分な
剛性および保形性を保持し得るものである。すな
わち前記熱可塑性樹脂フイルム2はガラス転移点
が100℃以上であるため100℃前後に加熱された場
合にも常温の場合と殆んど変らない剛性を保持で
き、それゆえ常温の場合はもちろん、電子レンジ
で加熱したときの発泡シートの剛性を積層フイル
ム層により補ない得て、食品容器として加熱した
際にもきわめて優れた剛性および保形性を具有す
るものである。
As mentioned above, in the food container of the present invention, the foam sheet 1, which is the main component thereof, is made of a mixed resin of polyphenylene ether resin and polystyrene resin, and this itself has good rigidity and heat resistance, and can be heated easily. In addition to being able to maintain considerable rigidity, especially when one side of this foam sheet 1 has a glass transition temperature of 100
Since it is laminated with a thermoplastic resin film 2 or a multilayer film of synthetic resin containing thermoplastic resin film 2 with a temperature of ℃ or above, rigidity and shape retention are important factors when used as a food container for direct cooking in a microwave oven. is further improved, and can maintain sufficient rigidity and shape retention even when heated. In other words, since the thermoplastic resin film 2 has a glass transition point of 100°C or higher, even when heated to around 100°C, it can maintain almost the same rigidity as at room temperature. The rigidity of the foam sheet when heated in a microwave oven is compensated for by the laminated film layer, and it has extremely excellent rigidity and shape retention even when heated as a food container.

殊に前記熱可塑性樹脂フイルム2が発泡シート
1の両面に積層されている場合、いわゆるスキ
ン・コア・スキンのサンドイツチ構造となり、力
学的な見地からも耐熱剛性発揮の上でさらに有効
である。しかも前記積層フイルム層によつて発泡
シート単独のものに比し耐水性や耐油性等の他の
属性も改善され、もちろん、発泡シート1による
断熱性や加熱された食品の保温性も良好である。
従つて、本考案の容器は、この種加熱調理用食品
容器として望まれる上記性能イ,ロ,ハ,ニ,
ホ,ヘおよびトをいずれも満足するものであり、
電子レンジで加熱調理できる食品容器として好適
に使用できる。さらに前記複合シートからの成形
性も良好なもので、第3図や第4図のごとき複雑
なトレイ形状の食品容器も容易に成形でき大量生
産可能で比較的安価に提供できる。
In particular, when the thermoplastic resin film 2 is laminated on both sides of the foamed sheet 1, a so-called skin-core-skin sandwich structure is formed, which is more effective in exhibiting heat-resistant rigidity from a mechanical standpoint. Moreover, other attributes such as water resistance and oil resistance are improved by the laminated film layer compared to the foam sheet alone, and of course, the foam sheet 1 also has good insulation properties and heat retention of heated foods. .
Therefore, the container of the present invention has the above-mentioned performances desired as a food container for heating and cooking.
It satisfies all of E, F and G,
It can be suitably used as a food container that can be heated in a microwave oven. Further, the moldability of the composite sheet is good, and food containers having complicated tray shapes as shown in FIGS. 3 and 4 can be easily molded, mass-produced, and provided at a relatively low cost.

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

図は本考案の実施例を示すものであり、第1図
は斜視図、第2図は前図−線における拡大断
面図、第3図および第4図は容器形状を異にした
一部欠截斜視図、第5図および第6図はそれぞれ
他の実施例を示す第2図相当断面図である。 A……食品容器、1……混合樹脂の発泡シー
ト、2……熱可塑性樹脂フイルム、3……他の樹
脂フイルム層。
The figures show an embodiment of the present invention, in which Fig. 1 is a perspective view, Fig. 2 is an enlarged sectional view taken along the line - front figure, and Figs. 3 and 4 are partially cutaway views of containers with different shapes. The cutaway perspective view, FIG. 5, and FIG. 6 are respectively sectional views corresponding to FIG. 2 showing other embodiments. A... Food container, 1... Foamed sheet of mixed resin, 2... Thermoplastic resin film, 3... Other resin film layer.

Claims (1)

【実用新案登録請求の範囲】 1 ポリフエニレンエーテル系樹脂10〜50重量%
とポリスチレン系樹脂90〜50重量%との混合樹
脂を素材とする発泡倍率3〜80倍、厚み1〜6
mmの発泡シートの少なくとも片面に、ガラス転
移点が100℃以上の熱加塑性樹脂フイルムまた
は同フイルムを含む合成樹脂の複層フイルムを
積層した複合シートから一体に成形されてなる
食品容器。 2 ガラス転移点100℃以上の熱可塑性樹脂フイ
ルムがポリカーボネート系樹脂からなる実用新
案登録請求の範囲第1項記載の食品容器。 3 複層シートは、容器内側表面層として、ポリ
オレフイン系樹脂、ポリエステル系樹脂、ポリ
塩化ビニリデン系樹脂、ポリアミド系樹脂のう
ちいずれか一の樹脂フイルム層が設けられてな
る実用新案登録請求の範囲第1項または第2項
記載の食品容器。
[Scope of claims for utility model registration] 1. Polyphenylene ether resin 10-50% by weight
Foaming ratio 3 to 80 times, thickness 1 to 6, made from a mixed resin of 90 to 50% by weight of polystyrene resin
A food container that is integrally formed from a composite sheet in which a thermoplastic resin film with a glass transition point of 100°C or higher or a multilayer film of a synthetic resin containing the same film is laminated on at least one side of a foam sheet of 1.0 mm in diameter. 2. The food container according to claim 1, wherein the thermoplastic resin film having a glass transition point of 100° C. or higher is made of polycarbonate resin. 3. The multilayer sheet is provided with a resin film layer of any one of polyolefin resin, polyester resin, polyvinylidene chloride resin, and polyamide resin as the inner surface layer of the container. The food container according to item 1 or 2.
JP11960683U 1983-07-29 1983-07-29 food containers Granted JPS6026835U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11960683U JPS6026835U (en) 1983-07-29 1983-07-29 food containers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11960683U JPS6026835U (en) 1983-07-29 1983-07-29 food containers

Publications (2)

Publication Number Publication Date
JPS6026835U JPS6026835U (en) 1985-02-23
JPS6331957Y2 true JPS6331957Y2 (en) 1988-08-25

Family

ID=30274434

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11960683U Granted JPS6026835U (en) 1983-07-29 1983-07-29 food containers

Country Status (1)

Country Link
JP (1) JPS6026835U (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001219523A (en) * 1999-11-30 2001-08-14 Jsp Corp Thermoforming laminated foam
JP2008094919A (en) * 2006-10-10 2008-04-24 Kyoei Sangyo Kk Heat-resistant foam
JP2013028711A (en) * 2011-07-28 2013-02-07 Fp Corp Heat-resistant polystyrene-based resin composition, heat resistant polystyrene-based resin foamed sheet, laminated sheet, and packaging container

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2562467B2 (en) * 1987-11-04 1996-12-11 呉羽化学工業株式会社 Thermoformed polyarylene sulfide food container and method of making the same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5432722U (en) * 1977-08-09 1979-03-03
JPS55165926A (en) * 1979-06-13 1980-12-24 Asahi Chem Ind Co Ltd Production of heat-resistant, highly foamed product
JPS5643054A (en) * 1979-09-18 1981-04-21 Akebono Brake Ind Co Ltd Double piping liquid pressure controller
JPS5746775A (en) * 1980-07-01 1982-03-17 Mobil Oil Corp Heat resisting and fat resisting vessel
JPS5759477U (en) * 1980-09-26 1982-04-08
JPS637765U (en) * 1986-07-01 1988-01-19

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5550123Y2 (en) * 1975-03-12 1980-11-21
JPS55120929U (en) * 1979-02-20 1980-08-27
JPS617076Y2 (en) * 1980-11-13 1986-03-04
JPS626406Y2 (en) * 1980-12-29 1987-02-14

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5432722U (en) * 1977-08-09 1979-03-03
JPS55165926A (en) * 1979-06-13 1980-12-24 Asahi Chem Ind Co Ltd Production of heat-resistant, highly foamed product
JPS5643054A (en) * 1979-09-18 1981-04-21 Akebono Brake Ind Co Ltd Double piping liquid pressure controller
JPS5746775A (en) * 1980-07-01 1982-03-17 Mobil Oil Corp Heat resisting and fat resisting vessel
JPS5759477U (en) * 1980-09-26 1982-04-08
JPS637765U (en) * 1986-07-01 1988-01-19

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001219523A (en) * 1999-11-30 2001-08-14 Jsp Corp Thermoforming laminated foam
JP2008094919A (en) * 2006-10-10 2008-04-24 Kyoei Sangyo Kk Heat-resistant foam
JP4699327B2 (en) * 2006-10-10 2011-06-08 共栄産業株式会社 Manufacturing method of heat-resistant resin container for food
JP2013028711A (en) * 2011-07-28 2013-02-07 Fp Corp Heat-resistant polystyrene-based resin composition, heat resistant polystyrene-based resin foamed sheet, laminated sheet, and packaging container

Also Published As

Publication number Publication date
JPS6026835U (en) 1985-02-23

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