JPS62149431A - Laminated product of polyolefin group resin foam - Google Patents

Laminated product of polyolefin group resin foam

Info

Publication number
JPS62149431A
JPS62149431A JP29042285A JP29042285A JPS62149431A JP S62149431 A JPS62149431 A JP S62149431A JP 29042285 A JP29042285 A JP 29042285A JP 29042285 A JP29042285 A JP 29042285A JP S62149431 A JPS62149431 A JP S62149431A
Authority
JP
Japan
Prior art keywords
foam
base material
product
polyolefin
laminated
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
JP29042285A
Other languages
Japanese (ja)
Other versions
JPH0353110B2 (en
Inventor
大久保 俊二
利治 中江
莞二 田中
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP29042285A priority Critical patent/JPS62149431A/en
Publication of JPS62149431A publication Critical patent/JPS62149431A/en
Publication of JPH0353110B2 publication Critical patent/JPH0353110B2/ja
Granted legal-status Critical Current

Links

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は成形性に優れたポリオレフィン系樹脂発泡体の
積層製品に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a laminated product of polyolefin resin foam having excellent moldability.

(従来の技術) 従来、ポリオレフィン系樹脂発泡体は、真空成形や圧縮
成形などにより各種の形態の製品として各種多用な用途
に使用されてきたが、これらの発泡体は発泡体単独で製
品化されることは少なく、通常ポリ塩化ビニルやポリオ
レフィンなどのプラスチックシートや布帛などの基材と
熱融着、接着剤などを用いて接合した積層製品の形で使
用されるのが普通であった。
(Prior art) Polyolefin resin foams have traditionally been used for a variety of purposes as products in various forms by vacuum forming, compression molding, etc. However, these foams have not been commercialized as individual foams. It was rarely used, and it was usually used in the form of a laminated product that was bonded to a base material such as a plastic sheet or fabric made of polyvinyl chloride or polyolefin using heat fusion or adhesive.

このような積層製品の成形性は、発泡体そのものの成形
性がよくても、該発泡体に積層されるべき基材の性質に
よって、積層製品そのものの成形性が著しく相違するた
めに、発泡体の成形性をいかに改良しても、基材の種類
によって成形性が相違してくるため、成形加工の際に積
層された発泡体層が破壊され、品質の良好な製品を1q
ることができないという問題があった。
The moldability of such laminated products differs significantly depending on the properties of the base material to be laminated to the foam, even if the foam itself has good moldability. No matter how much the moldability of the product is improved, the moldability will differ depending on the type of base material, so the laminated foam layers will be destroyed during the molding process, and 1q of good quality products will be lost.
The problem was that I couldn't do it.

(発明の解決しようとする問題点〉 本発明の目的は、このようなIi層される表皮基材の種
類により発泡体層が損傷を受けることがなく、良好な真
空成形性および圧縮成形性を有する積層製品を提供する
にある。
(Problems to be Solved by the Invention) The object of the present invention is to prevent the foam layer from being damaged by the type of skin base material used for the Ii layer, and to provide good vacuum moldability and compression moldability. To provide laminated products with:

(問題点を解決するための手段) このような本発明の目的は、 見掛密度が0.025〜0.100CI/cc、140
°Cにおける破断強度と破断伸度との積が少なくとも3
0Kq/cm2・%であり、かつ130〜190℃にお
ける成形絞り比が少なくとも0゜5であるポリオレフィ
ン系発泡体に50%および100%伸長時における引張
応力が前記ポリオレフィン系発泡体の2倍以下である表
皮基材を積層してなるポリオレフィン系樹脂発泡体の積
層製品によって達成することができる。
(Means for Solving the Problems) The object of the present invention is to provide an apparent density of 0.025 to 0.100 CI/cc, 140
The product of breaking strength and breaking elongation at °C is at least 3
0 Kq/cm2・% and a drawing ratio of at least 0°5 at 130 to 190°C, the tensile stress at 50% and 100% elongation is not more than twice that of the polyolefin foam. This can be achieved by a laminated product of polyolefin resin foam made by laminating certain skin base materials.

まず本発明において、積層製品を構成する発泡体は、0
.025〜0.100Q/cc範囲の見掛密度を有して
おり、かつ140℃における破断強度と破断伸度との積
が30Kg/cm2・5以上であるという特性を有する
ことが必要でおる。
First, in the present invention, the foam constituting the laminated product is
.. It is necessary to have an apparent density in the range of 0.025 to 0.100 Q/cc, and a product of breaking strength and breaking elongation at 140° C. of 30 Kg/cm 2 ·5 or more.

ここで見掛密度(C1/CC)は、発泡体を10cm角
に正確に裁断し、その手さと厚みを測定し、次式にした
がって算出した値である。
Here, the apparent density (C1/CC) is a value calculated by accurately cutting the foam into 10 cm square pieces, measuring the shape and thickness, and using the following formula.

見掛密度= 発泡体の重ffi/100x発泡体の厚さくCm)この
見掛密度の値が0.025Q/ccよりも小さくなると
、発泡体の応力が小さく、圧縮回復性および形態保持性
が十分でなく、成形加工品としての実用性能が満足され
ないために好ましくないし、また、0.100g/cc
よりも大きくなると、圧縮硬さが大きくなり、また緩衝
性(クッション性)が低下し、自動車の内装材などの成
形加工品として好ましいものではない。
Apparent density = Foam weight ffi/100x Foam thickness Cm) When the value of this apparent density is smaller than 0.025Q/cc, the stress of the foam is small, and the compression recovery and shape retention properties are low. 0.100g/cc
If it is larger than this, the compression hardness will increase and the cushioning properties will decrease, making it undesirable for molded products such as automobile interior materials.

そして、本発明の特徴は、後述する発泡体に積層される
べき表皮基材の特性と密接な関係を有するが、該発泡体
の140℃における破断強度と破断伸度との積が30K
g/cm2・5以上であることにある。
The feature of the present invention is closely related to the characteristics of the skin base material to be laminated to the foam, which will be described later.
g/cm2.5 or more.

ここで140℃における発泡体の破断強度および破断伸
度の測定法は、次のごとくして測定される値である。
Here, the breaking strength and breaking elongation of the foam at 140° C. are measured as follows.

島津製作所製のオートグラフl5−500型に加熱炉(
大栄科学精機社製)取付けた装置を使用し、試験体をJ
 Is−に−6301に規定されている測定法にしたが
ってダンベル(1号形)状に打扱き、J IS−に−6
767に規定されている測定法に準じて140℃下で引
張速度500mm/分で測定した。
A heating furnace (
Using the attached device (manufactured by Daiei Kagaku Seiki Co., Ltd.), the test specimen was
Handle it in a dumbbell shape (No. 1 shape) according to the measurement method specified in JIS-6301, and
Measurement was carried out at 140° C. and at a tensile speed of 500 mm/min according to the measuring method specified in 767.

なお、試験体の加熱時間は5分間とし、破断点強度およ
び伸度は記録紙上から算出した。一方、強度の単位につ
いては、発泡体単独の場合は単位面積当りの応力(Kq
/cm2 )で示し、表皮材と発泡体の応力とを比較を
する場合は、表皮材の厚さが小さいために試験片の巾当
り応力(Kch/cm)によって示した。
The heating time of the test specimen was 5 minutes, and the strength at break and elongation were calculated from the recording paper. On the other hand, regarding the unit of strength, in the case of a foam alone, the stress per unit area (Kq
When comparing the stress of the skin material and the foam, the stress per width of the test piece (Kch/cm) was used to compare the stress of the skin material and the foam because the thickness of the skin material was small.

上記測定法によって求められる破断強度と破断伸度の積
が30t4C7/cm2・%よりも低くなると、表皮基
材と貼合わせし、成形加工(真空、圧縮)した場合に、
発泡体が成形に必要な応力、伸び率が不足するため発泡
体が破れたり、ざらに貼合わせ界面で剥離が起きるなど
のトラブルを生じ、実用的な成型品を得ることができな
いために好ましくない。また、破断強度と破断伸度の積
の上限は、特に限定されないが、好ましくは約600K
に7Cm2・%がよい。
If the product of breaking strength and breaking elongation determined by the above measurement method is lower than 30t4C7/cm2・%, when laminated with the skin base material and molded (vacuum, compression),
This is undesirable because the foam lacks the stress and elongation necessary for molding, causing problems such as the foam breaking or peeling at the rough bonding interface, making it impossible to obtain a practical molded product. . Further, the upper limit of the product of breaking strength and breaking elongation is not particularly limited, but is preferably about 600K.
7 Cm2・% is good.

このような見掛密度および140℃における破断強度と
破断伸度の積とを有するポリオレフィン系樹脂発泡体の
製造法としては、こうらの各種ポリオレフイ系樹脂、た
とうばポリエチレン、ポリプロピレン、ポリエチレン−
プロピレン共単合体などを原料として、放射線架橋発泡
法および化学架橋発泡法などによって得ることができる
。具体的には、前記ポリオレフィン系樹脂に公知の熱分
解型発泡剤、たとえばアゾジカルボンアミド、ジニトロ
ソペンタメチレンテトラミンなどおよび必要に応じて加
熱によってラジカルを発生する架橋剤を混合し、前記の
発泡剤および架橋剤が分解しない温度に保持して成形、
たとえばシート状に成形する。この成形されたシート状
物を電離性放射線架橋法または化学的架橋法などの公知
の任意の方法を適用して、ゲル分率が15〜60%、好
ましくは20〜40%になるように架橋する。
As a method for producing a polyolefin resin foam having such an apparent density and the product of breaking strength and breaking elongation at 140°C, various polyolefin resins such as these, polyethylene, polypropylene, polyethylene-
It can be obtained by a radiation crosslinking foaming method, a chemical crosslinking foaming method, etc. using a propylene comonolymer as a raw material. Specifically, the polyolefin resin is mixed with a known thermally decomposable blowing agent, such as azodicarbonamide, dinitrosopentamethylenetetramine, etc., and, if necessary, a crosslinking agent that generates radicals by heating, and then the blowing agent is mixed with a crosslinking agent that generates radicals when heated. and molding by holding at a temperature where the crosslinking agent does not decompose.
For example, it is formed into a sheet. This formed sheet material is cross-linked by any known method such as ionizing radiation cross-linking method or chemical cross-linking method so that the gel fraction becomes 15-60%, preferably 20-40%. do.

より具体的には、電離性放射線架橋法の場合は、高エネ
ルギー線としてα、β、γ、X線、電子線、中性子線等
、通常は、高エネルギー電子線照射機を使用し、たとえ
ば1〜50M r a dの線量の電子線を該シート状
物に照射することにより架橋される。この場合に、本発
明のブレンドポリマに対し、0.1〜10重量部の公知
の各種架橋助剤、たとえばジビニルベンゼン、ジアリル
フタレート、トリメチロールプロパンミルリアクリレー
トなどを添加して電子線架橋してもよい。この放射線照
射に代えて、ベンゾフェノンなどの紫外線増感剤を添加
し、紫外線を照射して架橋することもできる。
More specifically, in the case of the ionizing radiation crosslinking method, α, β, γ, X-rays, electron beams, neutron beams, etc. are used as high-energy rays, and a high-energy electron beam irradiation machine is usually used. The sheet material is crosslinked by irradiating the sheet with an electron beam at a dose of ~50 M r a d. In this case, 0.1 to 10 parts by weight of various known crosslinking aids, such as divinylbenzene, diallyl phthalate, trimethylolpropanemyl acrylate, etc., are added to the blend polymer of the present invention and crosslinked with electron beams. Good too. Instead of this radiation irradiation, it is also possible to add an ultraviolet sensitizer such as benzophenone and crosslink by irradiating ultraviolet rays.

また、化学架橋法の場合は、ジクミルパーオキナイド、
ジターシャーリープチルパーオキサイドなどの有機過酸
化物ににる架1・n法、さらにこれらの架橋剤と共にビ
ニルトリメトキシシラン等のビニルシランを混練してグ
ラフ1〜化ざぜた後、シロキサン縮合反応によって架橋
させるシラン架橋法等を適宜適用することかできる。
In addition, in the case of chemical crosslinking method, dicumyl peroxinide,
Cross-linking method using an organic peroxide such as tertiary butyl peroxide, and further kneading vinyl silane such as vinyl trimethoxysilane with these cross-linking agents to form a compound (see graph 1), followed by cross-linking by siloxane condensation reaction. A silane crosslinking method or the like can be applied as appropriate.

かくして’+F7られる成型品は、熱風雰囲気中または
ツル1へ浴上で加熱され、成形品内部に含イ1される発
泡剤を急激に分解させることによって発泡体に変換され
る。
The molded article thus subjected to '+F7' is heated in a hot air atmosphere or on a bath to convert it into a foam by rapidly decomposing the blowing agent contained inside the molded article.

また、本発明の目的を損わない範囲で、本発明の発泡体
の製造に使用する前記組成物には、滑剤、酸化防止剤、
紫外線吸収剤、着色剤、帯電防止剤、難燃剤、その他の
各種添加物を所望の目的を達成し得る範囲内で配合する
ことができる。
In addition, to the extent that the object of the present invention is not impaired, the composition used for producing the foam of the present invention may include lubricants, antioxidants,
Ultraviolet absorbers, colorants, antistatic agents, flame retardants, and other various additives can be blended within the range that can achieve the desired purpose.

さらに、本発明に使用するポリオレフィン系樹脂発泡体
は、その少なくとも1面にコロナ放電処理、コーティン
グなどにより接着剤をイ」与し、ラミネート加工し、そ
の加工性の向上を図ることができるし、プラスデックフ
ィルムやシー1〜、他の発泡体シートや金属箔を貼り合
わせたり、押出ラミネートなどにより複合@造を付与し
たりする、すなわち各種の加工技術を適用することがで
きる。
Furthermore, the polyolefin resin foam used in the present invention can be laminated by applying an adhesive to at least one surface thereof by corona discharge treatment, coating, etc., to improve its workability. Various processing techniques can be applied, such as laminating PlusDeck film, Sea 1~, other foam sheets, or metal foils, or imparting a composite structure by extrusion lamination or the like.

このような見掛密度および140℃における破断強度と
破断伸度との積が30 K O/ c m 2・%以上
であるポリオレフィン系樹脂発泡体は、その真空成形絞
り比、特に130〜190℃下の真空成形絞り比が0.
5以上であることが好ましく、この真空成形絞り比率が
0.5以上であることによって、著しく優れた真空成形
性を積層製品に与えることができる。
A polyolefin resin foam having such an apparent density and a product of breaking strength and breaking elongation at 140°C of 30 K O/cm 2 % or more has a vacuum forming drawing ratio, particularly 130 to 190°C. The lower vacuum forming drawing ratio is 0.
It is preferably 5 or more, and by having this vacuum forming drawing ratio of 0.5 or more, extremely excellent vacuum formability can be imparted to the laminated product.

次に、このようなポリオレフィン系樹脂発泡体に積層さ
れる表皮基材としては、ポリ塩化ビニルシート、ポリオ
レフィンシート、ポウレタンシーi〜および繊維織物な
どがあるが、該表皮基材は、その50%および100%
伸長時における引張応力が前記ポリオレフィン系発泡体
の2.0倍以下、好ましくは1.5倍以下であることが
必要である。
Next, as skin base materials laminated on such polyolefin resin foam, there are polyvinyl chloride sheets, polyolefin sheets, polyurethane sheets, and fiber fabrics. % and 100%
It is necessary that the tensile stress during elongation is 2.0 times or less, preferably 1.5 times or less, than that of the polyolefin foam.

すなわち、該表皮基材の50%および100%伸長時に
おける引張応力がこれを積層する発泡体の2.0倍より
も大きくなると、成形加工さる段階で発泡体と表皮基材
の応力差によって、発泡体が破壊したり、貼り合わせ面
で剥離(界面剥離)を起こし、所望の成形加工品を得る
ことができなくなるために好ましくない。
That is, if the tensile stress of the skin base material at 50% and 100% elongation is greater than 2.0 times that of the foam on which it is laminated, due to the stress difference between the foam and the skin base material during the molding process, This is not preferable because the foam may be destroyed or peeling may occur at the bonded surfaces (interfacial peeling), making it impossible to obtain the desired molded product.

該発泡体への表皮基材の積層法としては、接着剤を用い
て両者を接合する方法、押出はによるラミネート法やフ
レーム(炎)法による接合方法などを挙げることができ
るが、特に限定されるものではない。
Methods for laminating the skin base material onto the foam include a method of bonding the two using an adhesive, a lamination method using extrusion, a bonding method using a flame method, etc., but there are no particular limitations. It's not something you can do.

[発明の効果] かくして得られる本発明の積層製品は、優れた真空成形
性および圧縮成形性をを付し、しかもその成形加工、特
に成形絞り比が0.5以上の成形の際に、積層された発
泡体層が表記桔材から剥離したり、破壊することかなく
、品質、形態に唖れたものである。
[Effect of the invention] The thus obtained laminated product of the present invention has excellent vacuum formability and compression moldability, and moreover, the laminated product has excellent vacuum formability and compression formability, and moreover, the laminated product has excellent vacuum formability and compression formability, and moreover, the laminated product has excellent vacuum formability and compression formability. The resulting foam layer did not peel off from the marking material or break, and the quality and shape were poor.

したがって、多くの用途において優れた成形性を有し、
たとえば自動車の内”A4’)J (ドアー、インスト
ルメントパネルなど)とじの複合成形での1〜ラブルが
ほとんど発生しない。
Therefore, it has excellent moldability in many applications,
For example, in the composite molding of the binding of "A4") J (doors, instrument panels, etc.) in automobiles, 1 to 1 - almost no trouble occurs.

以下、実施例により本発明の効果をより具体的に説明す
る。
EXAMPLES Hereinafter, the effects of the present invention will be explained in more detail with reference to Examples.

実施例1〜4、比較例1〜2 エチレンを4%ランダム共重合したメルトインデックス
(M ! )が1.5のポリプロピレン系樹脂70%に
Mlが2.01密度が0.930のポリエチレン樹脂3
0%、ざらに発泡剤としてアゾジカルボンアミド、架橋
助剤としてジビニルベンゼンおよび安定剤として“アイ
21ノール″を配合し、均一に混合した掛、押出機でシ
ートを成形した。
Examples 1 to 4, Comparative Examples 1 to 2 70% polypropylene resin with melt index (M!) of 1.5, which is made by random copolymerization of 4% ethylene, Ml is 2.01, and polyethylene resin 3 has a density of 0.930.
0%, azodicarbonamide as a foaming agent, divinylbenzene as a crosslinking aid, and "I-21Nol" as a stabilizer were mixed uniformly and then molded into a sheet using an extruder.

得られたシートに電子線を照射した後、加熱された塩浴
上で架橋、発泡させて、第1表に示した特性値を有する
・6種類の発泡体を作成した。
After irradiating the obtained sheet with an electron beam, it was crosslinked and foamed on a heated salt bath to create six types of foams having the characteristic values shown in Table 1.

これらの発泡体に表皮基材として、ポリ塩化ビニルシー
トを積層し、接着剤を用いて接合して積層シートを得た
。この積層シートを直径が500mmφ、深さが250
mm (L/D=0.5)の金型を用いて真空成形し、
底部の破壊(発泡体の破壊d′3よび接合面の界面剥離
)状態を調べて比較した。これらの結果を第1表に併せ
て示した。表から、本発明に規定する条件を満足する積
層1歿品の場合は、良好な真空成形性および圧縮成形性
を有すると共に、成形時に積層された発泡体が破壊した
り、該発泡体と表皮基材との接合面から剥離したりする
ことのない、極めて優れた別械的性能を有することが判
る。
A polyvinyl chloride sheet was laminated on these foams as a skin base material and bonded using an adhesive to obtain a laminated sheet. This laminated sheet has a diameter of 500 mmφ and a depth of 250 mm.
Vacuum forming using a mold of mm (L/D=0.5),
The state of destruction at the bottom (destruction d'3 of the foam and interfacial peeling of the joint surfaces) was investigated and compared. These results are also shown in Table 1. From the table, it can be seen that a laminated one-piece product that satisfies the conditions stipulated in the present invention has good vacuum formability and compression formability, and the laminated foam does not break during molding, and the foam and skin do not break during molding. It can be seen that it has extremely excellent mechanical performance without peeling from the joint surface with the base material.

Claims (2)

【特許請求の範囲】[Claims] (1)見掛密度が0.025〜0.100g/cc、1
40℃における破断強度と破断伸度との積が少なくとも
30Kg/cm^2・%であり、かつ130〜190℃
における成形絞り比が少なくとも0.5であるポリオレ
フィン系発泡体に50%および100%伸長時における
引張応力が前記ポリオレフィン系発泡体の2倍以下であ
る表皮基材を積層してなるポリオレフィン系樹脂発泡体
の積層製品。
(1) Apparent density is 0.025 to 0.100 g/cc, 1
The product of breaking strength and breaking elongation at 40°C is at least 30 Kg/cm^2%, and 130 to 190°C
A polyolefin resin foam formed by laminating a skin base material whose tensile stress at 50% and 100% elongation is not more than twice that of the polyolefin foam at 50% and 100% elongation to a polyolefin foam whose forming drawing ratio is at least 0.5. Body laminated products.
(2)、特許請求の範囲第1項において、表皮基材がポ
リ塩化ビニルシート、ポリオレフィンシート、ポウレタ
ンシートおよび繊維織物からなる群から得らばれた基材
であるポリオレフィン系樹脂発泡体の積層製品。
(2) In claim 1, the skin base material is a laminate of polyolefin resin foams whose skin base material is a base material obtained from the group consisting of a polyvinyl chloride sheet, a polyolefin sheet, a polyurethane sheet, and a fiber fabric. product.
JP29042285A 1985-12-25 1985-12-25 Laminated product of polyolefin group resin foam Granted JPS62149431A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29042285A JPS62149431A (en) 1985-12-25 1985-12-25 Laminated product of polyolefin group resin foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29042285A JPS62149431A (en) 1985-12-25 1985-12-25 Laminated product of polyolefin group resin foam

Publications (2)

Publication Number Publication Date
JPS62149431A true JPS62149431A (en) 1987-07-03
JPH0353110B2 JPH0353110B2 (en) 1991-08-14

Family

ID=17755825

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29042285A Granted JPS62149431A (en) 1985-12-25 1985-12-25 Laminated product of polyolefin group resin foam

Country Status (1)

Country Link
JP (1) JPS62149431A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0267129A (en) * 1988-08-31 1990-03-07 Toray Ind Inc Laminated molded body and preparation thereof
US5910358A (en) * 1996-11-06 1999-06-08 The Dow Chemical Company PVC-free foamed flooring and wall coverings
JP2011235775A (en) * 2010-05-11 2011-11-24 Tomei Kasei Kk Vehicle interior equipment, and skin material for vehicle interior used as skin material of the vehicle interior equipment
JP5980438B2 (en) * 2014-03-24 2016-08-31 リンテック株式会社 Processed product manufacturing method

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51112018A (en) * 1975-03-28 1976-10-04 Asahi Chem Ind Co Ltd Laminated interior material
JPS5720344A (en) * 1980-07-11 1982-02-02 Mitsui Petrochemical Ind Laminate
JPS57145130A (en) * 1981-03-03 1982-09-08 Furukawa Electric Co Ltd:The Heat-processable crosslinked polypropylene foam sheet
JPS60208233A (en) * 1984-04-02 1985-10-19 積水化学工業株式会社 Laminated sheet

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51112018A (en) * 1975-03-28 1976-10-04 Asahi Chem Ind Co Ltd Laminated interior material
JPS5720344A (en) * 1980-07-11 1982-02-02 Mitsui Petrochemical Ind Laminate
JPS57145130A (en) * 1981-03-03 1982-09-08 Furukawa Electric Co Ltd:The Heat-processable crosslinked polypropylene foam sheet
JPS60208233A (en) * 1984-04-02 1985-10-19 積水化学工業株式会社 Laminated sheet

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0267129A (en) * 1988-08-31 1990-03-07 Toray Ind Inc Laminated molded body and preparation thereof
JPH0622961B2 (en) * 1988-08-31 1994-03-30 東レ株式会社 Laminated molded article and method for producing the same
US5910358A (en) * 1996-11-06 1999-06-08 The Dow Chemical Company PVC-free foamed flooring and wall coverings
JP2011235775A (en) * 2010-05-11 2011-11-24 Tomei Kasei Kk Vehicle interior equipment, and skin material for vehicle interior used as skin material of the vehicle interior equipment
JP5980438B2 (en) * 2014-03-24 2016-08-31 リンテック株式会社 Processed product manufacturing method
JP2019021946A (en) * 2014-03-24 2019-02-07 リンテック株式会社 Protective film formation film
JP2019021945A (en) * 2014-03-24 2019-02-07 リンテック株式会社 Protective film formation film
US10510578B2 (en) 2014-03-24 2019-12-17 Lintec Corporation Protective film forming film, protective film forming sheet and work product manufacturing method

Also Published As

Publication number Publication date
JPH0353110B2 (en) 1991-08-14

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