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JPS60168733A - Polystyrene resin foam sheet - Google Patents

Polystyrene resin foam sheet

Info

Publication number
JPS60168733A
JPS60168733A JP59022900A JP2290084A JPS60168733A JP S60168733 A JPS60168733 A JP S60168733A JP 59022900 A JP59022900 A JP 59022900A JP 2290084 A JP2290084 A JP 2290084A JP S60168733 A JPS60168733 A JP S60168733A
Authority
JP
Japan
Prior art keywords
weight
styrene
polystyrene
sheet
foam sheet
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP59022900A
Other languages
Japanese (ja)
Other versions
JPH0449861B2 (en
Inventor
Jun Maeda
純 前田
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 BASF Co Ltd
Original Assignee
Mitsubishi Chemical BASF 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 Chemical BASF Co Ltd filed Critical Mitsubishi Chemical BASF Co Ltd
Priority to JP59022900A priority Critical patent/JPS60168733A/en
Publication of JPS60168733A publication Critical patent/JPS60168733A/en
Publication of JPH0449861B2 publication Critical patent/JPH0449861B2/ja
Granted legal-status Critical Current

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  • Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
  • Molding Of Porous Articles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Laminated Bodies (AREA)

Abstract

PURPOSE:The titled foam sheet rich in flexibility and suitable for the production of fruit trays, etc., prepared by mixing polystyrene with a styrene/butadiene/styrene block copolymer and a higher fatty acid metal salt and expansion-molding the mixture. CONSTITUTION:A resin composition comprising 100pts.wt. polystyrene (number- average MW of 8X10<4>-2.2X10<5>, weight-average MW of 10X10<4>-5X10<5>), 5- 20pts.wt. styrene/butadiene/styrene block copolymer (e.g., Toughprene, a product of Asahi Kasei Co., Ltd.), 0.2-5pts.wt. nucleating agent (e.g., talc or magnesium carbonate) and 0.05-1pt.wt. higher fatty acid metal salt (e.g., zinc stearate) is melted together with a blowing agent (a low-boiling organic compound) by heating in an extruder and expansion-molded through a die to form a sheet.

Description

【発明の詳細な説明】 本発明は、果物トレイ、鮮魚トレイ等の容器を真空成形
、圧空成形法により成形するに適したポリスチレン樹脂
発泡体シートに関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polystyrene resin foam sheet suitable for forming containers such as fruit trays and fresh fish trays by vacuum forming or pressure forming.

本発明の発泡体シートは柔軟性に富むので果物間の仕切
りとして用いる緩衝材として有用である。
Since the foam sheet of the present invention is highly flexible, it is useful as a cushioning material used as a partition between fruits.

ポリスチレン樹脂発泡体シート(いわゆるスチレンペー
パー)は、鮮魚、果物のトレイ成形用素材として使用さ
れている(実開昭58−92040号)。
A polystyrene resin foam sheet (so-called styrene paper) is used as a material for molding trays for fresh fish and fruits (Utility Model Application Publication No. 58-92040).

通常、かかるスチレンベーパーは、ポリス4−・ンペレ
ットと核剤、例えば硅砂、タルク、炭カル等とをミキサ
ーで混合した組成物を押出機のホッパーより供給し、こ
れを押出機で230〜250℃で溶融混練し、この溶融
混線物に押出様の途中に設けられたパイプよシブタン、
ペンタン、塩化メチレン、ジクロロジフルオロメタン等
の発泡剤を加えたのち、同押出機の冷却ゾーンで160
℃に冷却し、ついでグイより管状に押出発泡し、冷却後
、カッターによりこの管状発泡シートを二面に切り開い
て製造されている(特公昭43−15709号)。また
、このシートは、混練と冷却を別々の押出機を用いて製
造されることもある(特公昭42−25781号)。
Usually, such styrene vapor is produced by supplying a composition prepared by mixing polystyrene pellets and a nucleating agent such as silica sand, talc, charcoal, etc. in a mixer from a hopper of an extruder, and then extruding the mixture at 230 to 250°C. Shibutane is melted and kneaded, and a pipe is installed in the middle of the extrusion process to extrude the molten mixture.
After adding a blowing agent such as pentane, methylene chloride, dichlorodifluoromethane, etc., the cooling zone of the extruder
It is manufactured by cooling the sheet to 0.degree. C., then extruding it into a tubular foam using a goo, and after cooling, cutting the tubular foam sheet into two sides with a cutter (Japanese Patent Publication No. 15709/1983). In addition, this sheet may be produced using separate extruders for kneading and cooling (Japanese Patent Publication No. 25781/1989).

このようにして型造された肉厚が1〜3間、見掛密度が
0,05〜0.2f/crIKのポリスチレンベーパー
は真空成形され、鮮魚、野菜、肉等のトレイとして使用
されている。また、他のシート、例えば架橋ポリエチレ
ン発泡体シートと積層し、真空成形され、桃、梨等の果
物トレイとして部用されている。
The polystyrene vapor molded in this way with a wall thickness of 1 to 3 and an apparent density of 0.05 to 0.2 f/crIK is vacuum formed and used as a tray for fresh fish, vegetables, meat, etc. . It is also laminated with another sheet, such as a crosslinked polyethylene foam sheet, and vacuum formed to be used as a tray for fruits such as peaches and pears.

このポリスチレンペーパー製トレイは肉、魚介類の包装
資材として用いる場合、通常、ラップフィルムによりく
るまれて使用されるが、柔軟性(耐衝撃性)に乏しいた
めこのフィルムをラッグする際にトレイに捲装する力を
強くすると破損することがある。
When this polystyrene paper tray is used as a packaging material for meat and seafood, it is usually wrapped in cling film, but since it has poor flexibility (impact resistance), it is necessary to wrap the tray around the tray when wrapping this film. If you apply too much force, it may break.

本発明はかかる従来のスチレンペーパーノ欠点を、ポリ
スチレンにスチレン0ブタジエン・スチレンブロック共
重合体および高級脂肪酸の金属塩を添加することにより
柔軟性を向上させて解決を画るものである。
The present invention attempts to solve such drawbacks of conventional styrene paper by adding a styrene/butadiene/styrene block copolymer and a metal salt of a higher fatty acid to polystyrene to improve its flexibility.

即ち、本発明は (4)ポリスチレン ioo重量部 置部スチレン・ブタジェン・スチレンブロック共重合体
 5〜20重量部 0核剤 0.2 〜5重量部 0高級脂肪酸の金属塩 0.05〜1重量部上記(4)
、(8)、(C)および0成分を含有する樹脂組成物を
発泡剤を用いて発泡させて得たシートであって、該シー
トの見掛密度が0.05〜0.297dであることを特
徴とするポリスチレン樹脂発泡体シートを提供するもの
である。
That is, the present invention provides (4) polystyrene ioo parts by weight styrene-butadiene-styrene block copolymer 5 to 20 parts by weight 0 nucleating agent 0.2 to 5 parts by weight 0 metal salts of higher fatty acids 0.05 to 1 part by weight Above (4)
, (8), a sheet obtained by foaming a resin composition containing components (C) and 0 using a foaming agent, and having an apparent density of 0.05 to 0.297 d. The present invention provides a polystyrene resin foam sheet characterized by:

重量平均分子量(MY)が10 X 10’ −5X 
105のポリスチレンが使用できる。
Weight average molecular weight (MY) is 10X 10'-5X
105 polystyrene can be used.

(砂成分のスチレン・ブタジェン・スチレンブロック共
重合体は、平均分子量が25,000〜1.Oo o、
o o oOものが一般であり、米国シェル社よりカリ
フレック、’、TR1101、TR1102、TR11
84、TRI 107、TRIIII、TR1112の
商品名で、旭化成よりタフブレンの商品名で販売されて
いる。
(The styrene-butadiene-styrene block copolymer of the sand component has an average molecular weight of 25,000 to 1.000,
o o oO ones are common, and Cariflex, ', TR1101, TR1102, TR11 from Shell Company in the United States.
84, TRI 107, TRIII, and TR1112, and is sold by Asahi Kasei under the trade name Toughblen.

このスチレン―)゛タジエンースチレンフ゛ロック共重
合体はゴム質である。ポリスチレンの耐衝撃改良剤とし
て特開昭58−187436号にはSBR,NBR,ブ
ナゴム、HIPS、ブチルゴム等のゴム質が開示される
が、ポリスチレンとの相溶性ハ、スチレン−ブタジェン
Oスチレンブロック共重合体が一番優れる。
This styrene-)butadiene-styrene block copolymer is rubbery. JP-A-58-187436 discloses rubber materials such as SBR, NBR, buna rubber, HIPS, and butyl rubber as impact modifiers for polystyrene; Combination is the best.

このスチレン・ブタジェン・スチレンブロック共重合体
は、(4)成分100重量部に対して5〜20重量部の
割合で配合される。5重量部未満では耐衝撃性の改良効
果が低い。逆に20重量部を越えると得られるシートの
曲げ強度の低下が著しいので好ましくない。
This styrene-butadiene-styrene block copolymer is blended in a proportion of 5 to 20 parts by weight per 100 parts by weight of component (4). If the amount is less than 5 parts by weight, the effect of improving impact resistance will be low. On the other hand, if it exceeds 20 parts by weight, the bending strength of the resulting sheet will drop significantly, which is not preferable.

次に(0成分の核剤は、発泡体のセル径を均一に訓整す
るのに役立つものであり、タルク、炭酸マグネシウム、
パーライト、硅酸カルシウム、炭酸カルシウム、酸化硅
素、バライタ、バーミキュライト等の無機系核剤、クエ
ン酸、酒石酸、硼酸、蓚酸等の有機酸が用いられる。
Next, the nucleating agent (component 0) is useful for uniformly adjusting the cell diameter of the foam, and is made of talc, magnesium carbonate,
Inorganic nucleating agents such as perlite, calcium silicate, calcium carbonate, silicon oxide, baryta, and vermiculite, and organic acids such as citric acid, tartaric acid, boric acid, and oxalic acid are used.

この核剤は、■成分のポリスチレン100重量部に対し
て0.2〜−重量部の割合で用いる。
This nucleating agent is used in a proportion of 0.2 to -2 parts by weight per 100 parts by weight of polystyrene as component (1).

0成分の高級脂肪酸の金属塩としては、炭素数が12〜
22の高級脂肪酸、例えばカプリン酸、ステアリン酸、
バルミチン酸等の金属塩(Ca。
As a metal salt of higher fatty acid with 0 components, carbon number is 12~
22 higher fatty acids, such as capric acid, stearic acid,
Metal salts such as valmitic acid (Ca.

Na、K、Li、 Zn、 At)があげられる。特に
ステアリン酸亜鉛、ステアリン酸アルミニウム及びステ
アリン酸カルシウムが好適である。
Examples include Na, K, Li, Zn, At). Particularly suitable are zinc stearate, aluminum stearate and calcium stearate.

この高級脂肪酸の金属塩は、シートを押出成形する際の
加工性を向上させるとともに、発泡体シートの柔軟性を
向上する。この高級脂肪酸の金属塩は、囚成分のポリス
チレン100重量部に対して0.05〜1重量部の割合
で用いる。0.05重量部未満ではシートの柔軟性の改
良効果が小さい。
This metal salt of higher fatty acid improves the processability during extrusion molding of the sheet and also improves the flexibility of the foam sheet. This metal salt of higher fatty acid is used in a proportion of 0.05 to 1 part by weight per 100 parts by weight of polystyrene as the prison component. If the amount is less than 0.05 part by weight, the effect of improving the flexibility of the sheet is small.

1重量部を越えては、シートの製膜安定性が悪化すると
いう欠点がある。
If the amount exceeds 1 part by weight, there is a drawback that the film forming stability of the sheet deteriorates.

この(4)、(Bl、(Qおよび■成分を含有する樹脂
組成物は低沸点有機化合物を発泡剤としてこれを押出機
内で加熱溶融させ、ダイよシ円筒状に押出発泡させてシ
ート状に成形される。その発泡剤は既述したように押出
機にパイプより圧入してもよいが、予じめポリスチレン
樹脂組成物に発泡剤を含浸させ、次いでこれを押出機の
ホッパーより供給し、溶融混線、押出発泡して成形して
もよい。
The resin composition containing components (4), (Bl, (Q and The foaming agent may be press-fitted into the extruder through a pipe as described above, but the polystyrene resin composition is impregnated with the foaming agent in advance, and then this is supplied from the hopper of the extruder. It may also be molded by melt mixing or extrusion foaming.

本発明の発泡体シートを熱成形して得たトレイは、耐衝
撃性が良好でおる。
The tray obtained by thermoforming the foam sheet of the present invention has good impact resistance.

以下、実施例により本発明を更に詳細に説明する。Hereinafter, the present invention will be explained in more detail with reference to Examples.

実施例1 (4)下記の物性を有するポリメチレフ100部数平均
分子量 2.OX 105 重量平均分子量 1.OX 10’ (均スチレンーブタジェン・スチレンブロック共重合体
“カリフレックス1102” 10部 C)タルク 2.5部 (2)ステアリン酸亜鉛 0.3部 上記樹脂組成物を第1押出機に供給し、押出機で230
℃、150 Kf/、、iGの条件で樹脂を溶融混練し
、そこで230℃のブタンを注入口よシ160Kf/c
r/lGで圧入し、ブタンガスを4%の割合で含む混合
物を押出機内のスクリューで押出機の冷却ゾーンに移し
、この冷却ゾーンでブタンガスと溶融ポリスチレンとの
混合をスクリュー混練してよシ均一とするとともに15
0℃迄冷却した。
Example 1 (4) Polymethylef 100 parts average molecular weight having the following physical properties 2. OX 105 Weight average molecular weight 1. OX 10' (homogeneous styrene-butadiene-styrene block copolymer "Califlex 1102" 10 parts C) Talc 2.5 parts (2) Zinc stearate 0.3 parts The above resin composition was supplied to the first extruder 230 with an extruder
The resin was melted and kneaded under the conditions of 150 Kf/, iG at 150 Kf/c, and then butane at 230°C was poured into the injection port at 160 Kf/c.
The mixture containing butane gas at a ratio of 4% is transferred to the cooling zone of the extruder using a screw inside the extruder, and in this cooling zone, the mixture of butane gas and molten polystyrene is kneaded by the screw to make it uniform. and 15
Cooled to 0°C.

ついで円筒ダイ上り口径100 m Bのインフレーシ
ョンシートを押出し、このシートをマンドレルで内部冷
却するとともに拡径し、次いでマンドレルよシ離れる部
分でこのインフレーションシートの1ケ所をカットし、
1枚の発泡体シートとして引きとった(引取速度5m/
分)。
Next, a cylindrical die extrudes an inflation sheet with an upward diameter of 100 m B, and this sheet is internally cooled and expanded in diameter with a mandrel. Next, the inflation sheet is cut at one place at the part separated from the mandrel.
It was collected as a single foam sheet (collection speed 5m/
minutes).

発泡体シートの平均肉厚は約2.3mであシ、シート幅
は790闇あり、見掛密度は0.09t/diであった
The average wall thickness of the foam sheet was approximately 2.3 m, the sheet width was 790 mm, and the apparent density was 0.09 t/di.

この発泡体シートを、真空成形機を用いて170℃で加
熱、溶融させ、15個取りの型を用い、真空(450m
 Hg )成形を行ない、次いでトリミングして平均肉
厚が3.Off、縦195■、横126鱈、深さ22m
mのトレイを15個得た。
This foam sheet was heated and melted at 170°C using a vacuum forming machine, and then vacuum molded (450 m
Hg) Molding and then trimming until the average wall thickness is 3. Off, length 195cm, width 126mm, depth 22m
15 m trays were obtained.

このトレーの両横を手で把み、長手方向に瞬時に90度
折り曲げだ際の割れ方により、その段階を次の4段階に
数値化し、耐脆性の目安(数値力;小さい程よい)とし
た。結果は0であった。
Grasp both sides of this tray with your hands and instantaneously bend it 90 degrees in the longitudinal direction, and the breakage will be evaluated, and the level of breakage will be digitized into the following four levels, and used as a guideline for brittleness resistance (numerical force; the lower the better). . The result was 0.

0=割れなかった。0 = Not broken.

1=底部又は両側部のどちらか一方のみ割れ目が発生す
る。
1 = Cracks occur only on either the bottom or both sides.

2=両側部の双方又は両側部のどちらか一方と底部に割
れ目が発生する。
2 = Cracks occur on both sides or either side and the bottom.

3=両側部の双方と底部いずれにも割れ目が発生する。3=Cracks occur on both sides and the bottom.

又、高滓製作所製オートグラフを用い、前記トレーの長
手中心部を底面より突き上げる形で三点曲げ試験を行っ
た。この時の曲げ強度は、2.0Kfであった。
In addition, a three-point bending test was conducted using an autograph manufactured by Takasugi Seisakusho in which the longitudinal center of the tray was pushed up from the bottom surface. The bending strength at this time was 2.0 Kf.

更に前記オートグラフを用い、トレー長手方向の両測部
中心を両側よりはさみ込む形で12.5m変形させた際
のトレーの反撥力をめたところ、o、s Kfであった
。この反撥力が大きいと、トレーを用いて、包装する時
、ラップフィルムをトレーに被せ、ラップフィルムを張
る時のしめつけ力に対抗できやすくなる。すなわち、薄
いシートでも使用でき、コスト低減となる。
Furthermore, using the autograph described above, the repulsive force of the tray when the tray was deformed by 12.5 m in such a manner that the centers of both measurement parts in the longitudinal direction were sandwiched from both sides was calculated and was found to be o,s Kf. If this repulsive force is large, when packaging using a tray, it becomes easier to resist the tightening force when the wrap film is placed over the tray and the wrap film is stretched. That is, even a thin sheet can be used, resulting in cost reduction.

更に、柔軟性は、IKg / dの荷重を厚さ10咽の
素材(シートを10鰭になる様に重ね合わせる。)に加
えたときの圧縮歪(慎)で示した。この値の大きい素材
はど柔かいといえる。結果は、0.8mmであった。
Furthermore, flexibility was expressed as compressive strain (Shin) when a load of IKg/d was applied to a material with a thickness of 10 fins (sheets were overlapped to form 10 fins). Materials with a large value can be said to be soft. The result was 0.8 mm.

実施例2〜4、比較例1〜3 懺(81,(C”lおよびυ成分の組成を表1に示すよ
うに変更する他は実施例1と同様にして発泡体シートを
得、真空成形してトレイを得た。
Examples 2 to 4, Comparative Examples 1 to 3 Foam sheets were obtained in the same manner as in Example 1, except that the compositions of the C"l and υ components were changed as shown in Table 1, and vacuum formed. And got the tray.

シート、トレイの物性を表1に示す。Table 1 shows the physical properties of the sheet and tray.

比較例4 (B)成分ノスチレンeブタジェン・スチレンブロック
共重合体(SBS)の代りに、スチレン・フ゛タジエン
ランダム共重合体ゴム(SBR)を用いる他は実施例1
と同様にして発泡体シートを得、真空成形してトレイを
得た。
Comparative Example 4 Example 1 except that styrene-butadiene random copolymer rubber (SBR) was used instead of component (B) nostyrene e-butadiene-styrene block copolymer (SBS).
A foam sheet was obtained in the same manner as above, and a tray was obtained by vacuum forming.

シート、トレイの物性を表1に示す。Table 1 shows the physical properties of the sheet and tray.

Claims (1)

【特許請求の範囲】 1)、(4)ポリスチレン 100重量部(9)スチレ
ン−ブタジェン−スチレンブロック共重合体 5〜20
重量部 (0核剤 0.2〜5重量部 (1))高級脂肪酸の金属塩 0.05〜1重量部上記
(A)、(2)、(Qおよび■成分を含有する樹脂組成
物を発泡剤を用いて発泡させて得たシートであって、該
シートの見掛密度が0.05〜o、2y/−であること
を特徴とするポリスチレン樹脂発泡体シート。 2)、高級脂肪酸の金属塩がステアリン酸亜鉛、ステア
リン酸カルシウムまたはステアリン酸アルミニウムであ
ることを特徴とする特許請求の範囲第1項記載の発泡体
シート。
[Claims] 1), (4) Polystyrene 100 parts by weight (9) Styrene-butadiene-styrene block copolymer 5 to 20 parts by weight
Part by weight (0 nucleating agent 0.2 to 5 parts by weight (1)) Metal salt of higher fatty acid 0.05 to 1 part by weight A resin composition containing the above (A), (2), (Q and A polystyrene resin foam sheet obtained by foaming using a foaming agent, characterized in that the sheet has an apparent density of 0.05 to 0.2y/-.2) Higher fatty acid A foam sheet according to claim 1, characterized in that the metal salt is zinc stearate, calcium stearate or aluminum stearate.
JP59022900A 1984-02-13 1984-02-13 Polystyrene resin foam sheet Granted JPS60168733A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59022900A JPS60168733A (en) 1984-02-13 1984-02-13 Polystyrene resin foam sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59022900A JPS60168733A (en) 1984-02-13 1984-02-13 Polystyrene resin foam sheet

Publications (2)

Publication Number Publication Date
JPS60168733A true JPS60168733A (en) 1985-09-02
JPH0449861B2 JPH0449861B2 (en) 1992-08-12

Family

ID=12095518

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59022900A Granted JPS60168733A (en) 1984-02-13 1984-02-13 Polystyrene resin foam sheet

Country Status (1)

Country Link
JP (1) JPS60168733A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003026876A (en) * 2001-07-23 2003-01-29 Idemitsu Petrochem Co Ltd Aromatic vinyl resin composition and molding thereof
JP2019019163A (en) * 2017-07-12 2019-02-07 東洋スチレン株式会社 Styrenic resin composition and molding prepared therewith

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5569638A (en) * 1978-11-20 1980-05-26 Asahi Chem Ind Co Ltd High-specific-gravity styrene resin composition
JPS5669638A (en) * 1979-11-09 1981-06-11 Fuji Photo Film Co Ltd Production of function separation type electrophotographic receptor
JPS5699635A (en) * 1980-01-14 1981-08-11 Sekisui Plastics Co Ltd Preparation of styrene resin foam plate of large thickness
JPS58101026A (en) * 1981-12-12 1983-06-16 Sekisui Plastics Co Ltd Continuous manufacture of polystyrene foamed and molded item

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5569638A (en) * 1978-11-20 1980-05-26 Asahi Chem Ind Co Ltd High-specific-gravity styrene resin composition
JPS5669638A (en) * 1979-11-09 1981-06-11 Fuji Photo Film Co Ltd Production of function separation type electrophotographic receptor
JPS5699635A (en) * 1980-01-14 1981-08-11 Sekisui Plastics Co Ltd Preparation of styrene resin foam plate of large thickness
JPS58101026A (en) * 1981-12-12 1983-06-16 Sekisui Plastics Co Ltd Continuous manufacture of polystyrene foamed and molded item

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003026876A (en) * 2001-07-23 2003-01-29 Idemitsu Petrochem Co Ltd Aromatic vinyl resin composition and molding thereof
JP2019019163A (en) * 2017-07-12 2019-02-07 東洋スチレン株式会社 Styrenic resin composition and molding prepared therewith

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