JPH0976340A - High gloss food container lid - Google Patents

High gloss food container lid

Info

Publication number
JPH0976340A
JPH0976340A JP23968495A JP23968495A JPH0976340A JP H0976340 A JPH0976340 A JP H0976340A JP 23968495 A JP23968495 A JP 23968495A JP 23968495 A JP23968495 A JP 23968495A JP H0976340 A JPH0976340 A JP H0976340A
Authority
JP
Japan
Prior art keywords
rubber
weight
resin
food container
gloss
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.)
Withdrawn
Application number
JP23968495A
Other languages
Japanese (ja)
Inventor
Hiroshi Mikami
宏 三上
Jun Sugiyama
潤 杉山
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP23968495A priority Critical patent/JPH0976340A/en
Publication of JPH0976340A publication Critical patent/JPH0976340A/en
Withdrawn legal-status Critical Current

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  • Packging For Living Organisms, Food Or Medicinal Products That Are Sensitive To Environmental Conditiond (AREA)
  • Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a high gloss food container lid composed of a rubber modified styrenic resin having high glooss, high impact strength, high rigidity and high surface hardness and especially used as yoghurt. SOLUTION: In a rubber modified styrenic resin containing a rubbery elastomer as dispersing particles, a resin phase is a polymer consisting of 30-70wt.% of a styrenic monomer (a) and 70-30wt.% of an acrylic ester monomer (b) and the average particle size of rubber particles of a dispersion phase is 0.3-2.0μm. A sheet obtained from the rubber modified styrenlc resin containing 5-15wt.% of the rubbery elastomer is thermoformed to obtain a food container.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術用分野】本発明は、ゴム変性スチレ
ン系樹脂より得られたシートよりなる食品容器に関す
る。更に詳しくは、表面光沢が85%以上で、光沢性に
優れたゴム変性スチレン系樹脂よりなるシートで、高光
沢食品容器蓋に関する。
TECHNICAL FIELD The present invention relates to a food container comprising a sheet obtained from a rubber-modified styrene resin. More specifically, the present invention relates to a high-gloss food container lid, which is a sheet made of a rubber-modified styrene resin having a surface gloss of 85% or more and excellent in gloss.

【0002】[0002]

【従来技術】食品容器蓋は加工性、印刷性、強度の点か
ら樹脂製品が急速に普及している。高光沢を必要とする
蓋材料は、硬質PVCが主流である。しかし、廃棄物処
理問題及びリサイクル問題等により、代替え材料が求め
られている。代表的な代替え材料としてはゴム変性ポリ
スチレン樹脂の使用が検討されているが、熱成形品の光
沢が充分でない。また、ポリスチレンとスチレン−ブタ
ジエンブロック共重合体との混合物が検討されているが
光沢が充分でないこと、衝撃強度が低いこと、剛性が低
いこと、表面硬度が低いこと等の問題点があり、あまり
実用化されていない。また、このスチレン−ブタジエン
ブロック共重合体はブレンド中にゲル状物質が押出機で
発生して成形品の外観や、印刷時のインク飛び不良等の
悪影響を与えるため、PVC代替え材料としては実用性
に乏しい。
2. Description of the Related Art Resin products for food container lids are rapidly becoming widespread because of their workability, printability and strength. Hard PVC is the mainstream for lid materials that require high gloss. However, alternative materials are required due to waste disposal problems, recycling problems, and the like. The use of rubber-modified polystyrene resin as a typical alternative material has been examined, but the gloss of the thermoformed product is not sufficient. Further, a mixture of polystyrene and a styrene-butadiene block copolymer has been studied, but there are problems such as insufficient gloss, low impact strength, low rigidity, and low surface hardness. It has not been put to practical use. In addition, this styrene-butadiene block copolymer is a practicable PVC substitute material because a gel-like substance is generated in the extruder during blending, which adversely affects the appearance of the molded product and the defective ink ejection during printing. Poor.

【0003】[0003]

【発明が解決しようとする課題】本発明は高光沢を有
し、衝撃強度が高く、剛性が高く、表面硬度が高いゴム
変性スチレン系樹脂よりなる食品容器、特にヨーグルト
容器に使用される高光沢食品容器蓋に適するシートを提
供するものである。
The present invention has a high gloss, a high impact strength, a high rigidity, and a food container made of a rubber-modified styrenic resin having a high surface hardness, particularly a high gloss used for a yogurt container. A sheet suitable for a food container lid is provided.

【0004】[0004]

【課題を解決するための手段】すなわち、本発明は、ゴ
ム状弾性体を分散粒子として含有するゴム変性スチレン
系樹脂に於いて、樹脂相(母相)は(イ)スチレン系単
量体30〜70重量%、(ロ)アクリル酸エステル系単
量体70〜30重量%からなる重合体であり、分散相の
ゴム粒子平均粒子径が0.3〜2.0μmの範囲であ
り、ゴム状弾性体を5〜15重量%含有するゴム変性ス
チレン系樹脂よりなるシートを熱成形することを特徴と
する食品容器である。
That is, the present invention relates to a rubber-modified styrene resin containing a rubber-like elastic material as dispersed particles, wherein the resin phase (mother phase) is (a) styrene monomer 30. To 70% by weight and 70% to 30% by weight of (b) acrylic acid ester-based monomer, the dispersed phase has a rubber particle average particle size in the range of 0.3 to 2.0 μm, and has a rubber-like shape. A food container is characterized in that a sheet made of a rubber-modified styrene resin containing 5 to 15% by weight of an elastic body is thermoformed.

【0005】本発明のゴム変性スチレン系樹脂よりなる
シートを熱成形したものは、表面光沢が85%以上で、
光沢性に優れたゴム変性スチレン系樹脂よりなるシート
で、高光沢食品容器蓋に適するものである。以下に本発
明の詳細を説明する。本発明においてゴム変性スチレン
系樹脂を構成するスチレン系単量体としては、スチレ
ン、α−メチルスチレン、t−ブチルスチレン、p−メ
チルスチレン等が使用できる。これらスチレン系単量体
は単独または混合して使用できる。アクリル酸エステル
系単量体として、メチルメタクリレート、ブチルアクリ
レート、ブチルメタクリレート、エチルアクリレート等
が使用できる。これらアクリル酸エステル単量体は単独
または混合して使用できる。
A sheet formed by thermoforming the rubber-modified styrenic resin of the present invention has a surface gloss of 85% or more,
A sheet made of rubber-modified styrenic resin with excellent gloss, suitable for high-gloss food container lids. The details of the present invention will be described below. In the present invention, styrene, α-methylstyrene, t-butylstyrene, p-methylstyrene and the like can be used as the styrene monomer constituting the rubber-modified styrene resin. These styrene monomers can be used alone or in combination. As the acrylic acid ester-based monomer, methyl methacrylate, butyl acrylate, butyl methacrylate, ethyl acrylate, etc. can be used. These acrylate monomers can be used alone or in combination.

【0006】スチレン系単量体及びアクリル酸エステル
系単量体の構成比は、スチレン系単量体が30〜70重
量%からなる重合体からなることが必要である。スチレ
ン系単量体が30%未満ではゴム変性スチレン系樹脂の
特徴である加工性が著しく低下し好ましくなく、70%
を越えると光沢性が不充分となる。本発明のゴム変性ス
チレン系樹脂の分散相となるゴム成分としては、ポリブ
タジエンゴム、スチレン−ブタジエンゴムを使用するこ
とが出来る。分散相のゴム粒子径は0.3〜2.0μm
である。粒子径が0.3未満では衝撃強度が著しく低下
し好ましくない。粒子径が2.0μm以上では熱成形品
の光沢が低下し好ましくない。
The composition ratio of the styrene-based monomer and the acrylate-based monomer is required to be a polymer in which the styrene-based monomer is 30 to 70% by weight. If the styrene-based monomer content is less than 30%, the processability, which is a characteristic of the rubber-modified styrene-based resin, is significantly reduced, which is not preferable, and 70%
If it exceeds, the glossiness becomes insufficient. Polybutadiene rubber and styrene-butadiene rubber can be used as the rubber component serving as the dispersed phase of the rubber-modified styrenic resin of the present invention. The rubber particle diameter of the dispersed phase is 0.3 to 2.0 μm
It is. If the particle size is less than 0.3, the impact strength is significantly reduced, which is not preferable. When the particle size is 2.0 μm or more, the gloss of the thermoformed product is lowered, which is not preferable.

【0007】ゴム変性スチレン系樹脂に使用されるゴム
状弾性体量は衝撃強度の発現に重要でありスチレン系樹
脂に5〜15重量%含有する事が必要である。好ましく
は8〜15重量%である。ゴム状弾性体量が5%未満で
は強度補強効果が充分ではない。15重量%越える場合
は重合工程での生産性が低下し好ましくない。本発明の
ゴム粒子の平均粒子径は、ゴム変性スチレン系樹脂ペレ
ットをジメチルホルムアミドを溶媒としてレーザー光散
乱測定法により測定した。
The amount of the rubber-like elastic material used in the rubber-modified styrenic resin is important for developing impact strength, and it is necessary that the styrene-based resin be contained in an amount of 5 to 15% by weight. It is preferably 8 to 15% by weight. If the amount of the rubber-like elastic material is less than 5%, the strength reinforcing effect is not sufficient. If it exceeds 15% by weight, the productivity in the polymerization step is lowered, which is not preferable. The average particle diameter of the rubber particles of the present invention was measured by a laser light scattering measurement method using rubber-modified styrene resin pellets with dimethylformamide as a solvent.

【0008】本発明のゴム変性スチレン系樹脂には熱可
塑性エラストマーを添加することができる。添加できる
エラストマーとしてはSBR系の熱可塑性ゴムがよく、
例えば、日本合成ゴム(株)製TR−2000、旭化成
工業(株)製タフプレン125或いは126が好まし
い。また、添加する熱可塑性エラストマー量はゴム変性
スチレン系樹脂100重量%に対し10重量%以下が好
ましく、より好ましくは8重量%以下である。10重量
%を越えると押出機でゲル状物質が発生して成形品の外
観や印刷時のインク飛び不良現象の起こる可能性があ
る。
A thermoplastic elastomer can be added to the rubber-modified styrenic resin of the present invention. As the elastomer that can be added, SBR type thermoplastic rubber is preferable,
For example, TR-2000 manufactured by Nippon Synthetic Rubber Co., Ltd. and Toughprene 125 or 126 manufactured by Asahi Kasei Kogyo Co., Ltd. are preferable. The amount of the thermoplastic elastomer added is preferably 10% by weight or less, more preferably 8% by weight or less, based on 100% by weight of the rubber-modified styrene resin. If it exceeds 10% by weight, a gel-like substance is generated in the extruder, and there is a possibility that the appearance of the molded product or the phenomenon of defective ink ejection during printing may occur.

【0009】本発明で用いられるテルペン系樹脂は、ゴ
ム変性スチレン系樹脂100重量部に対して1〜15重
量部含有することが望ましい。該テルペン樹脂は無水状
態で不活性雰囲気下で塩化アルミニウムに代表される強
ルイス酸を触媒としたフリーデルクラフツ重合により芳
香族ビニル系炭化水素とテルペンをカチオン共重合する
ことにより合成される。ここで言うテルペンとは柑橘系
皮質から得られるd−リモネン、生松脂から得られたα
−ピネンの異性化で得られるペンテン等を言う。本発明
におけるテルペン系樹脂には、テルペン系樹脂を水素添
加することによって得られる部分水素添加テルペン系樹
脂も含まれる。水素添加量については特に規定はないが
10モル%以上の芳香環を残す必要がある。これはテル
ペン系樹脂の芳香族環が無くなると重合段階で母相であ
るスチレン相(マトリックス)との分散相との相溶性、
或いは接着性が悪くなり機械的強度の低下を招く。
The terpene resin used in the present invention is preferably contained in an amount of 1 to 15 parts by weight based on 100 parts by weight of the rubber-modified styrene resin. The terpene resin is synthesized by cation copolymerization of an aromatic vinyl hydrocarbon and a terpene by Friedel-Crafts polymerization using a strong Lewis acid represented by aluminum chloride as a catalyst in an anhydrous state under an inert atmosphere. The terpenes referred to here are d-limonene obtained from citrus cortex and α obtained from raw pine resin.
-Pentene and the like obtained by isomerization of pinene. The terpene resin in the present invention also includes a partially hydrogenated terpene resin obtained by hydrogenating the terpene resin. The hydrogenation amount is not particularly limited, but it is necessary to leave 10 mol% or more of the aromatic ring. This is the compatibility with the dispersed phase with the styrene phase (matrix) which is the mother phase at the polymerization stage when the aromatic ring of the terpene resin disappears,
Alternatively, the adhesiveness deteriorates and the mechanical strength decreases.

【0010】テルペン系樹脂としては例えばヤスハラケ
ミカル(株)製、YSレジン、TΟ125、TΟ11
5、TΟ105及びTΟ85が、部分水素添加系として
は例えばヤスハラケミカル(株)製、クリアロンM10
5、M115が用いられる。テルペン系樹脂の添加は、
重合後のゴム変性スチレン系樹脂と押出し機でブレンド
して得ることが出来る。また、予め混練押出機でゴム成
分の中に押出し混練したもの、又はエチルベンゼン等の
揮発性有機溶媒に溶解させたものを重合液に混合して重
合させることによって行うことも可能である。
Examples of the terpene-based resin include YS resin, T 125 and T 11 manufactured by Yasuhara Chemical Co., Ltd.
5, T105 and T85 are, for example, CLEARON M10 manufactured by Yasuhara Chemical Co., Ltd. as a partial hydrogenation system.
5, M115 is used. The addition of terpene resin is
It can be obtained by blending with a rubber-modified styrene resin after polymerization with an extruder. It is also possible to carry out polymerization by mixing a mixture obtained by extruding and kneading into a rubber component in advance with a kneading extruder or dissolving in a volatile organic solvent such as ethylbenzene in a polymerization solution.

【0011】本発明のスチレン系樹脂は、通常のハイイ
ンパクトポリスチレンの製造方法を用いる事が出来る。
即ち、未架橋ゴムを重合液に溶解し、この原料液を撹拌
機付き反応器に供給し、重合を行う。ゴム粒径の粒径制
御は良く知られている一般的な方法、即ち樹脂成分(マ
トリックス)PSの分子量によるもの、或いは撹拌器の
回転数の増減に依って成し遂げられる。
The styrene-based resin of the present invention can be produced by a conventional method for producing high-impact polystyrene.
That is, an uncrosslinked rubber is dissolved in a polymerization liquid, and this raw material liquid is supplied to a reactor equipped with a stirrer to perform polymerization. The control of the rubber particle diameter can be achieved by a well-known general method, that is, by the molecular weight of the resin component (matrix) PS, or by increasing or decreasing the rotation speed of the stirrer.

【0012】重合するに当たってはその重合原料液にエ
チルベンゼン、トルエン或いはキシレン等の溶媒を用い
ることも可能である。また重合効率を高める為に過酸化
ベンゾイルに代表される様な有機過酸化物、或いはアゾ
ビスブチロニトリルに代表されるラジカル発生剤を重合
初期、あるいは重合途中で加えることも出来る。未反応
物の溜去は一般のポリスチレンに用いられるフラッシュ
タンクシステム、或いは押出し機に多段ベント付きシス
テムを搭載したものが好ましい。その際、水や不活性気
体を溶融樹脂に注入するとより効果的である。未反応単
量体および重合溶媒等を除去しペレットされる。
In the polymerization, it is possible to use a solvent such as ethylbenzene, toluene or xylene for the polymerization raw material liquid. To increase the polymerization efficiency, an organic peroxide such as benzoyl peroxide or a radical generator such as azobisbutyronitrile can be added at the beginning of the polymerization or during the polymerization. The unreacted material is preferably distilled off by using a flash tank system used for general polystyrene or an extruder equipped with a multi-vented system. At this time, it is more effective to inject water or an inert gas into the molten resin. Unreacted monomers and polymerization solvent are removed and pelletized.

【0013】本発明で用いられるテルペン系樹脂はゴム
質重合体を溶解した原料溶液に溶解するか、あるいは、
重合途中に加熱溶融状態であるいは溶媒に溶解して添加
するか、あるいは、回収系を出た後、加熱溶融状態で添
加するか、あるいは、ゴム変性スチレン系樹脂とテルペ
ン系樹脂をブレンドし、押出機で溶融混連する方法で添
加することが出来る。
The terpene resin used in the present invention is dissolved in a raw material solution in which a rubbery polymer is dissolved, or
During the polymerization, it is added in the molten state under heating or dissolved in a solvent, or after leaving the recovery system, it is added in the molten state under heating, or a rubber-modified styrene resin and a terpene resin are blended and extruded. It can be added by a method of melt-mixing with a machine.

【0014】本発明で用いられる熱可塑性エラストマー
はゴム変性スチレン系樹脂とブレンドし、押出機で溶融
混連する方法で添加することが出来る。本発明における
シート成形機は通常のスチレン系樹脂で使用されている
機械を使用することが出来るが、ユナイテッド・モール
ド(株)製のベルト式シート押出機を用いると光沢の優
れたシートを得ることが出来る。シート成形条件として
は、樹脂温度が190〜230℃、冷却ロール温度が5
0〜65℃の範囲を選択することが好ましい。
The thermoplastic elastomer used in the present invention can be added by blending it with a rubber-modified styrene resin and melt-mixing with an extruder. The sheet forming machine in the present invention may be a machine used for ordinary styrenic resins, but if a belt type sheet extruder manufactured by United Mold Co. is used, a sheet having excellent gloss can be obtained. Can be done. As the sheet forming conditions, the resin temperature is 190 to 230 ° C. and the cooling roll temperature is 5
It is preferable to select the range of 0 to 65 ° C.

【0015】シートの二次熱成形方法としては真空成
形、圧空成形、および熱板加熱式圧空成形等を選択する
ことが出来る。成形条件としては、ヒターゾーンの雰囲
気温度を180〜240℃、加熱時間を5〜6秒に設定
することが好ましい。シートの光沢はシーティング時に
ロールタッチ、または、ベルト式押出機を利用すること
により十分に高めることが可能であるが、樹脂が本来持
っていない光沢を加工条件で発現させたシートは二次熱
成形でいわゆる艶もどり現象によって光沢を失い本来の
光沢に戻ってしまう。
As the secondary thermoforming method for the sheet, vacuum forming, pressure forming, hot plate heating type pressure forming or the like can be selected. As molding conditions, it is preferable to set the ambient temperature in the hitter zone to 180 to 240 ° C. and the heating time to 5 to 6 seconds. The gloss of the sheet can be sufficiently increased by using a roll touch or a belt type extruder at the time of sheeting, but the sheet that expresses the gloss originally not possessed by the resin under the processing conditions is the secondary thermoforming. Then, due to the so-called luster restoration phenomenon, the gloss is lost and the original gloss is restored.

【0016】[0016]

【発明の実施の形態】BEST MODE FOR CARRYING OUT THE INVENTION

【0017】[0017]

【実施例1】撹拌機を備えた反応器2基を直列に連結
し、スチレン42.5重量%、ブチルアクリレート9.
1重量%、メチルメタクリレート38.2重量%を混合
し、更に、エチルベンゼン2.7重量%を加えた。この
混合物にゴム状弾性体7.5重量%を分散溶融させる。
その後重合反応を入り口温度が100℃、出口での温度
が150℃に設定された連続重合槽で行った。未反応単
量体を留去するために真空脱気にかけ、残留揮発分を5
00ppm以下にした。
Example 1 Two reactors equipped with a stirrer were connected in series, and 42.5% by weight of styrene and butyl acrylate were used.
1% by weight and 38.2% by weight of methyl methacrylate were mixed, and 2.7% by weight of ethylbenzene was further added. 7.5% by weight of a rubber-like elastic material is dispersed and melted in this mixture.
Thereafter, the polymerization reaction was carried out in a continuous polymerization tank in which the inlet temperature was set at 100 ° C. and the outlet temperature was set at 150 ° C. Vacuum degassing was carried out to distill off unreacted monomer, and residual volatile matter was reduced to 5
It was made less than 00 ppm.

【0018】上記操作にて得られたゴム変性スチレン系
重合体100重量部に対し、熱可塑性エラストマー(タ
フプレン126)を5.0重量部、およびテルペン系樹
脂(クリアロンM115)6.5重量部を単軸押出し機
で造粒して表1に示すゴム変性スチレン系樹脂組成物−
1を得た。この組成物100重量部に対し加工チタン3
重量部を加えシート押出機にて厚さ0.35mmのシー
トを得た。その後、圧空成形によりヨコ110mm×タ
テ85mm、深さ20mmの蓋を成形した。
With respect to 100 parts by weight of the rubber-modified styrenic polymer obtained by the above operation, 5.0 parts by weight of the thermoplastic elastomer (Tuffprene 126) and 6.5 parts by weight of the terpene resin (Clearlon M115) are added. Rubber-modified styrenic resin composition shown in Table 1 obtained by granulating with a single-screw extruder-
1 was obtained. Processed titanium 3 to 100 parts by weight of this composition
A weight of 0.35 mm was obtained with a sheet extruder. After that, a lid having a width of 110 mm, a length of 85 mm, and a depth of 20 mm was formed by pressure molding.

【0019】なお、構成単位の割合は、熱分解ガスクロ
マトグラフィーを用いて定量した。得られたシートのデ
ュポン衝撃強度と光沢度、および、熱成形蓋の光沢度を
表2に示す。光沢度はASTM:D523−67により
測定した。
The proportion of the constituent units was quantified by pyrolysis gas chromatography. Table 2 shows the DuPont impact strength and gloss of the obtained sheet, and the gloss of the thermoformed lid. The glossiness was measured according to ASTM: D523-67.

【0020】[0020]

【実施例2】テルペン系樹脂を添加しない以外は、実施
例1と同様に操作し、表1に示したゴム変性スチレン系
樹脂組成物−2を得、表2に示す物性を得た。
Example 2 A rubber-modified styrene resin composition-2 shown in Table 1 was obtained in the same manner as in Example 1 except that the terpene resin was not added, and the physical properties shown in Table 2 were obtained.

【0021】[0021]

【比較例1】ゴム状弾性体を2.0重量部に変更した以
外は、実施例1と同様に操作し、表1に示したゴム変性
スチレン系樹脂組成物−3を得、表2に示す物性を得
た。
Comparative Example 1 The procedure of Example 1 was repeated except that the rubber-like elastic material was changed to 2.0 parts by weight to obtain the rubber-modified styrene resin composition-3 shown in Table 1, and Table 2 The physical properties shown were obtained.

【0022】[0022]

【比較例2】重合時の撹拌機回転速度を速めた以外は、
実施例1と同様に操作し、表1に示したゴム変性スチレ
ン系樹脂組成物−4を得、表2に示す物性を得た。
Comparative Example 2 Except for increasing the rotation speed of the stirrer during polymerization,
By operating in the same manner as in Example 1, a rubber-modified styrenic resin composition-4 shown in Table 1 was obtained, and physical properties shown in Table 2 were obtained.

【0023】[0023]

【比較例3】ブチルアクリレート、およびメチルメタク
リレート使用しない以外は、実施例1と同様に操作し、
表1に示したゴム変性スチレン系樹脂組成物−5を得、
表2に示す物性を得た。
[Comparative Example 3] The same operation as in Example 1 was carried out except that butyl acrylate and methyl methacrylate were not used,
The rubber-modified styrene resin composition-5 shown in Table 1 was obtained,
The physical properties shown in Table 2 were obtained.

【0024】[0024]

【比較例4】スチレン21.6重量%、ブチルアクリレ
ート10.2重量%、メチルメタクリレート54.2重
量%、エチルベンゼン10.3重量%、ゴム状弾性体
3.7重量%とした以外は、実施例1と同様に操作し、
表1に示したゴム変性スチレン系樹脂組成物−6を得、
表2に示す物性を得た。
[Comparative Example 4] Except that 21.6% by weight of styrene, 10.2% by weight of butyl acrylate, 54.2% by weight of methyl methacrylate, 10.3% by weight of ethylbenzene, and 3.7% by weight of rubber-like elastic material. Operate as in Example 1,
The rubber-modified styrene resin composition-6 shown in Table 1 was obtained,
The physical properties shown in Table 2 were obtained.

【0025】[0025]

【表1】 [Table 1]

【0026】[0026]

【表2】 [Table 2]

【0027】[0027]

【発明の効果】本発明のゴム変性スチレン系樹脂組成物
から得られたシートより成形された食品容器蓋は、高光
沢度および衝撃強度に優れていることがわかる。本発明
のゴム変性スチレン系樹脂組成物から熱成形された蓋は
高意匠性を必要とする、ヨーグルト容器等の蓋材に最適
である。
EFFECTS OF THE INVENTION It can be seen that the food container lid formed from the sheet obtained from the rubber-modified styrene resin composition of the present invention is excellent in high gloss and impact strength. The lid thermoformed from the rubber-modified styrenic resin composition of the present invention is most suitable for a lid material such as a yogurt container that requires high designability.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ゴム状弾性体を分散粒子として含有する
ゴム変性スチレン系樹脂に於いて、樹脂相(母相)は
(イ)スチレン系単量体30〜70重量%、(ロ)アク
リル酸エステル系単量体70〜30重量%からなる重合
体であり、分散相のゴム粒子平均粒子径が0.3〜2.
0μmの範囲であり、ゴム状弾性体を5〜15重量%含
有するゴム変性スチレン系樹脂より得られたシートを熱
成形することを特徴とする食品容器。
1. A rubber-modified styrenic resin containing a rubber-like elastic material as dispersed particles, wherein the resin phase (mother phase) is (a) styrene-based monomer 30 to 70% by weight, and (b) acrylic acid. It is a polymer composed of 70 to 30% by weight of an ester monomer, and the average particle size of rubber particles in the dispersed phase is 0.3 to 2.
A food container characterized by thermoforming a sheet obtained from a rubber-modified styrenic resin having a rubber-like elastic body in an amount of 0 μm in an amount of 5 to 15% by weight.
【請求項2】 ゴム変性スチレン系樹脂100重量部あ
たり熱可塑性エラストマー1〜10重量部を加えること
を特徴とする請求項1記載の食品容器。
2. The food container according to claim 1, wherein 1 to 10 parts by weight of the thermoplastic elastomer is added to 100 parts by weight of the rubber-modified styrene resin.
【請求項3】 ゴム変性スチレン系樹脂100重量部あ
たりテルペン系樹脂1〜15重量部を加えることを特徴
とする請求項1又は2記載の食品容器。
3. The food container according to claim 1, wherein 1 to 15 parts by weight of the terpene resin is added to 100 parts by weight of the rubber-modified styrene resin.
JP23968495A 1995-09-19 1995-09-19 High gloss food container lid Withdrawn JPH0976340A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23968495A JPH0976340A (en) 1995-09-19 1995-09-19 High gloss food container lid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23968495A JPH0976340A (en) 1995-09-19 1995-09-19 High gloss food container lid

Publications (1)

Publication Number Publication Date
JPH0976340A true JPH0976340A (en) 1997-03-25

Family

ID=17048380

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23968495A Withdrawn JPH0976340A (en) 1995-09-19 1995-09-19 High gloss food container lid

Country Status (1)

Country Link
JP (1) JPH0976340A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004075196A (en) * 2002-07-31 2004-03-11 Shikoku Kakoki Co Ltd Hermetic container and its manufacturing method
JP2004075197A (en) * 2002-07-31 2004-03-11 Shikoku Kakoki Co Ltd Hermetic container and its manufacturing method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004075196A (en) * 2002-07-31 2004-03-11 Shikoku Kakoki Co Ltd Hermetic container and its manufacturing method
JP2004075197A (en) * 2002-07-31 2004-03-11 Shikoku Kakoki Co Ltd Hermetic container and its manufacturing method
JP4538207B2 (en) * 2002-07-31 2010-09-08 四国化工機株式会社 Sealed container and manufacturing method thereof

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