JPH09226034A - Foamed laminated sheet for automobile interior material - Google Patents
Foamed laminated sheet for automobile interior materialInfo
- Publication number
- JPH09226034A JPH09226034A JP8035016A JP3501696A JPH09226034A JP H09226034 A JPH09226034 A JP H09226034A JP 8035016 A JP8035016 A JP 8035016A JP 3501696 A JP3501696 A JP 3501696A JP H09226034 A JPH09226034 A JP H09226034A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- foamed
- automobile interior
- laminated sheet
- layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Molding Of Porous Articles (AREA)
- Laminated Bodies (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は変性ポリフェニレンエー
テル(以下、変性PPEと略す)系樹脂発泡層に非発泡
層を積層した耐熱性が改善された、軽量で成形性、遮音
性、断熱性、耐衝撃性に優れ、安価な自動車内装材用発
泡積層シートに関するものである。TECHNICAL FIELD The present invention relates to a modified polyphenylene ether (hereinafter abbreviated as modified PPE) resin foamed layer in which a non-foamed layer is laminated to improve heat resistance, and is lightweight, formable, soundproof, and heat insulating. The present invention relates to an inexpensive foam laminated sheet for automobile interior materials, which has excellent impact resistance.
【0002】[0002]
【従来技術】従来、自動車内装材として、熱可塑性樹脂
発泡体を主体とする基材にウレタンフォームを積層した
ものや、スチレン−無水マレイン酸共重合体の発泡層の
上下面にスチレン−無水マレイン酸共重合体の非発泡層
を積層した積層シートを所望の形状に成形したものが広
く用いられている。それらの自動車内装材は、軽量で断
熱性が高く、成形加工性がすぐれているという特徴があ
る。しかしながら、従来の自動車内装材、特に自動車天
井基材は、高温に長時間曝されるような用途に用いた場
合に、耐熱性が不十分であるため自重で垂れ下がる(ヒ
ートサグ)などの問題を発生することがあった。2. Description of the Related Art Conventionally, as an automobile interior material, a urethane foam laminated on a base material mainly composed of a thermoplastic resin foam, or styrene-maleic anhydride on the upper and lower surfaces of a foamed layer of a styrene-maleic anhydride copolymer. A laminate sheet formed by laminating a non-foamed layer of an acid copolymer into a desired shape is widely used. These automobile interior materials are characterized by being lightweight, having high heat insulating properties, and having excellent moldability. However, conventional automobile interior materials, especially automobile ceiling base materials, when used in applications where they are exposed to high temperatures for a long time, have problems such as hanging down under their own weight (heat sag) due to insufficient heat resistance. There was something to do.
【0003】そこで、耐熱性を向上させるために、耐熱
性の高い変性PPE系樹脂発泡層の上下面に変性PPE
系樹脂非発泡層を積層した発泡積層シートを用いた自動
車内装材用発泡積層シートが提案されている(実開平4
−11162号公報)。この変性PPE系樹脂を用いた
自動車内装材用発泡積層シートは、耐熱性に優れ軽量で
あるため高温下でのヒートサグが改善されるとされてい
るものである。一方、近年自動車車内空間の快適性が重
要視されるようになり、車内空間にゆとりを持たせるた
め室内を広くとるようになっている。このため自動車天
井基材一般においての軽薄化が実施されており、自動車
天井基材の耐熱性及び寸法安定性への品質要求がさらに
厳しくなっている。Therefore, in order to improve heat resistance, modified PPE is formed on the upper and lower surfaces of the modified PPE resin foam layer having high heat resistance.
A foamed laminated sheet for automobile interior materials using a foamed laminated sheet in which a non-foamed resin-based layer is laminated has been proposed (Actual Kaihei 4
-11162). The foamed laminated sheet for automobile interior materials using the modified PPE resin is excellent in heat resistance and is lightweight, and is said to have improved heat sag at high temperatures. On the other hand, in recent years, the emphasis has been placed on the comfort of the vehicle interior space, and the interior space of the automobile has become large in order to provide room for the interior space. For this reason, the weight reduction of general automobile ceiling base materials has been carried out, and the quality requirements for heat resistance and dimensional stability of automobile ceiling base materials have become more severe.
【0004】そこで、これらの問題を解決するために、
従来は無機質のガラス繊維とプラスチックの複合材料を
ベースとした自動車内装材が使用されてきた。しかし、
この構造では、耐熱性という品質は維持できるものの、
軽量化が図れない上にコスト高になるといった問題があ
った。[0004] In order to solve these problems,
Conventionally, automobile interior materials based on composite materials of inorganic glass fibers and plastics have been used. But,
With this structure, although the quality of heat resistance can be maintained,
There is a problem that the weight cannot be reduced and the cost becomes high.
【0005】[0005]
【発明が解決しようとしている課題】本発明は上記の如
き実情に鑑み、優れた耐熱性(非ヒートサグ性)を有す
るとともに優れた寸法安定性を有し、安価且つ容易に製
造可能な自動車内装材用発泡積層シートを提供するもの
である。In view of the above situation, the present invention has an excellent heat resistance (non-heat sag property) and an excellent dimensional stability, and can be manufactured inexpensively and easily in an automobile interior material. The present invention provides a foam laminated sheet for use.
【0006】[0006]
【課題を解決するための手段】本発明者らは耐熱特性を
維持しつつ軽量化を図るため、変性PPE系樹脂発泡層
を使用し、自動車内装材用発泡積層シートの構成を種々
変化させ鋭意検討を行った結果、非発泡層の熱可塑性樹
脂に無機フィラーを混合することにより、耐熱性に優
れ、かつ線膨張係数の抑制にも効果があることから、優
れた寸法変化率を示すものが得られることを見いだし
た。本発明者らは、自動車内装材用発泡層の少なくとも
片面に無機フィラーを含む非発泡層を使用する事で、軽
量で従来にない耐熱性の高い良好な寸法安定性、成形
性、耐衝撃性、遮音性、断熱性、コスト競争力を有する
変性PPE系樹脂の自動車内装材用発泡積層シートを発
明するに至った。[Means for Solving the Problems] In order to reduce the weight while maintaining the heat resistance, the present inventors have diligently changed the structure of the foam laminated sheet for automobile interior materials by using the modified PPE resin foam layer. As a result of the examination, by mixing an inorganic filler with the thermoplastic resin of the non-foamed layer, it has excellent heat resistance and is effective in suppressing the linear expansion coefficient. I found what I could get. The present inventors have used a non-foamed layer containing an inorganic filler on at least one side of a foamed layer for automobile interior materials, which is lightweight and has high heat resistance that has never been obtained. Good dimensional stability, moldability, and impact resistance. The inventors have invented a foamed laminated sheet for a vehicle interior material of a modified PPE resin having sound insulation, heat insulation and cost competitiveness.
【0007】上記課題を解決するために本発明は、自動
車内装材として変性PPE系樹脂発泡層の少なくとも片
面に無機フィラーを含む熱可塑性樹脂、好ましくは変性
PPE系樹脂からなる非発泡層を積層した自動車内装材
用発泡積層シートを提供する。また、上記課題を解決す
るために本発明は、非発泡層が熱可塑性樹脂100重量
部に対し、1〜50重量部の無機フィラーを含有せしめ
た自動車内装材用発泡積層シートを内容とする。In order to solve the above-mentioned problems, according to the present invention, a thermoplastic resin containing an inorganic filler, preferably a non-foamed layer made of a modified PPE resin is laminated on at least one surface of a modified PPE resin foam layer as an automobile interior material. Provided is a foamed laminated sheet for automobile interior materials. Moreover, in order to solve the said subject, this invention contains the foaming laminated sheet for automotive interior materials in which the non-foaming layer contains 1-50 weight part inorganic filler with respect to 100 weight part thermoplastic resin.
【0008】また、上記課題を解決するために本発明
は、無機フィラーを含む非発泡層を発泡層の上面(車内
天井面側)に使用された自動車内装材用発泡積層シート
を内容とする。また、上記課題を解決するために本発明
は、無機フィラーを含む非発泡層として、変性ポリフェ
ニレンエーテル系樹脂を基材樹脂として使用した自動車
内装材用発泡積層シートを内容とする。Further, in order to solve the above-mentioned problems, the present invention provides a foam laminated sheet for an automobile interior material in which a non-foam layer containing an inorganic filler is used on the upper surface of the foam layer (the ceiling surface side in the vehicle). Further, in order to solve the above problems, the present invention provides a foamed laminated sheet for automobile interior materials, which uses a modified polyphenylene ether resin as a base resin as a non-foamed layer containing an inorganic filler.
【0009】また、上記課題を解決するために本発明
は、発泡層がPPE成分25〜70重量部とポリスチレ
ン成分30〜75重量部であるPPE系樹脂とPS系樹
脂の混合樹脂、フェニルエーテルとスチレンとのグラフ
ト共重合樹脂、または該共重合樹脂とPS系樹脂との混
合樹脂からなる変性PPE系樹脂を基材樹脂として、該
基材樹脂に発泡剤を添加し押出発泡させて得られる一次
厚みが1〜5mm、一次発泡倍率が3〜20倍、セル径
が0.05〜0.3mm、独立気泡率が70%以上の発泡
層を構成要件とする自動車内装材用発泡積層シートを内
容とする。In order to solve the above-mentioned problems, according to the present invention, a foam layer comprises 25 to 70 parts by weight of a PPE component and 30 to 75 parts by weight of a polystyrene component, a mixed resin of a PPE resin and a PS resin, and phenyl ether. Primary obtained by using a modified PPE resin made of a graft copolymer resin with styrene or a mixed resin of the copolymer resin and a PS resin as a base resin, adding a foaming agent to the base resin, and extruding and foaming the resin. A foam laminated sheet for automobile interior material, which has a thickness of 1 to 5 mm, a primary expansion ratio of 3 to 20 times, a cell diameter of 0.05 to 0.3 mm, and a foam layer having a closed cell ratio of 70% or more as contents. And
【0010】本発明において使用される変性PPE系樹
脂発泡層の製造方法としては、変性PPE系樹脂に各種
の添加剤を加え、押出機により溶融・混練し、高温高圧
下で発泡剤を圧入し、発泡最適温度に調節して低圧帯
(通常大気中)に押出した後、マンドレル等によってシ
ート状に成形する方法が好適である。変性PPE系樹脂
発泡層の基材樹脂としてはPPEとPSの混合樹脂及び
フェニルエーテルとスチレンとのグラフト共重合体、該
共重合体とPS系樹脂の混合樹脂等が挙げられるが、製
造が容易である点でPPEとPSの混合樹脂が好まし
い。The method for producing the modified PPE resin foam layer used in the present invention is to add various additives to the modified PPE resin, melt and knead with an extruder, and press the foaming agent under high temperature and high pressure. A suitable method is to adjust the foaming optimum temperature, extrude into a low pressure zone (usually in the atmosphere), and then form into a sheet by a mandrel or the like. Examples of the base resin of the modified PPE resin foam layer include a mixed resin of PPE and PS, a graft copolymer of phenyl ether and styrene, a mixed resin of the copolymer and PS resin, etc. A mixed resin of PPE and PS is preferable in that
【0011】本発明において使用されるPPE系樹脂重
合用単量体としては例えば、2,6−ジメチルフェニレ
ン−1,4−エーテル、2−メチル−6−エチルフェニ
レン−1,4−エーテル、2,6−ジエチルフェニレン
−1,4−エーテル、2−メチル−6−n−プロピルフ
ェニレン−1,4−エーテル、2−メチル−6−n−ブ
チルフェニレン−1,4−エーテル、2−メチル−6−
クロルフェニレン−1,4−エーテル、2−メチル−6
−ブロムフェニレン−1,4−エーテル、2−エチル−
6−クロルフェニレン−1,4−エーテル等が挙げら
れ、これらは単独又は2種以上組み合わせて用いられ
る。Examples of the PPE resin polymerization monomer used in the present invention include 2,6-dimethylphenylene-1,4-ether, 2-methyl-6-ethylphenylene-1,4-ether and 2 , 6-Diethylphenylene-1,4-ether, 2-methyl-6-n-propylphenylene-1,4-ether, 2-methyl-6-n-butylphenylene-1,4-ether, 2-methyl- 6-
Chlorphenylene-1,4-ether, 2-methyl-6
-Bromphenylene-1,4-ether, 2-ethyl-
6-Chlorophenylene-1,4-ether and the like can be mentioned, and these can be used alone or in combination of two or more kinds.
【0012】フェニルエーテルとグラフト共重合される
スチレン系モノマー、又はPPEとブレンドされるポリ
スチレン重合用スチレン系モノマーとしては、例えばス
チレン、α−メチルスチレン、2,4−ジメチルスチレ
ン、モノクロルスチレン、ジクロルスチレン、p−メチ
ルスチレン、エチルスチレン等が挙げられる。上記ポリ
フェニレンエーテル、ポリスチレンのいずれにおいて
も、それぞれと重合可能な化合物、例えばアクリロニト
リル、メタクリロニトリル、メチル(メタ)アクリレー
ト、エチル(メタ)アクリレート、ブチル(メタ)アク
リレート、無水マレイン酸等を1種又は2種以上重合さ
せたものも含む。Examples of the styrene-based monomer graft-copolymerized with phenyl ether or the styrene-based monomer for polystyrene polymerization blended with PPE include styrene, α-methylstyrene, 2,4-dimethylstyrene, monochlorostyrene and dichloro. Examples thereof include styrene, p-methylstyrene, ethylstyrene and the like. In any of the above-mentioned polyphenylene ether and polystyrene, a compound capable of being polymerized with each of them, for example, acrylonitrile, methacrylonitrile, methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, maleic anhydride, etc. Also includes those obtained by polymerizing two or more kinds.
【0013】上記したポリフェニレンエーテルとスチレ
ン系化合物のグラフト共重合体を製造する方法は、従来
周知の方法でよく、例えば特公昭52−30991、特
公昭52−38596、特公昭52−142799号等
に開示されているものである。変性PPE系樹脂発泡層
の製造において使用される発泡剤としてはブタン、プロ
パン、ペンタン、塩化メチル、ジクロロメタン、クロロ
フロロメタン、ジクロロエタン、ジクロロジフロロエタ
ン等の炭化水素、ハロゲン化炭化水素等が挙げられ、ま
たそれらを組み合わせて使用しても良い。The above-mentioned method for producing a graft copolymer of polyphenylene ether and a styrene compound may be a conventionally known method, for example, Japanese Patent Publication Nos. 52-30991, 52-38596 and 52-142799. It is disclosed. Examples of the foaming agent used in the production of the modified PPE-based resin foam layer include hydrocarbons such as butane, propane, pentane, methyl chloride, dichloromethane, chlorofluoromethane, dichloroethane, dichlorodifluoroethane, and halogenated hydrocarbons. Alternatively, they may be used in combination.
【0014】本発明において使用される変性PPE系樹
脂発泡層の基材樹脂は、必要に応じて気泡調整剤、耐衝
撃性改良剤、滑剤、酸化防止剤、静電防止剤、顔料等を
添加することができる。本発明において、変性PPE系
樹脂を基材樹脂とする発泡シートはPPE成分25〜7
0重量部とポリスチレン成分75〜30重量部であるP
PEとPSの混合樹脂及びフェニルエーテルとスチレン
とのグラフト共重合体、該共重合体とPS系樹脂の混合
樹脂等を基材樹脂として、該基材樹脂に発泡剤を添加し
押出発泡させて得られる一次厚みが1〜5mm、一次発
泡倍率が3〜20倍、セル径が0.05〜0.3mm、独
立気泡率が70%以上であることが好ましい。PPE3
0〜65重量部とポリスチレン成分35〜70重量部が
さらに好ましく、PPE35〜60重量部とポリスチレ
ン成分40〜65重量部がさらにいっそう好ましい。ま
た、発泡シート中の残存揮発成分の量は1〜5重量部、
好ましくは2〜4重量部である。The base resin of the modified PPE resin foam layer used in the present invention may contain a cell regulator, an impact resistance improver, a lubricant, an antioxidant, an antistatic agent, a pigment, etc., if necessary. can do. In the present invention, the foamed sheet using the modified PPE resin as the base resin is the PPE component 25 to 7
P, which is 0 to 30 parts by weight and 75 to 30 parts by weight of polystyrene component
Using a mixed resin of PE and PS, a graft copolymer of phenyl ether and styrene, a mixed resin of the copolymer and PS resin as a base resin, and adding a foaming agent to the base resin for extrusion foaming. The obtained primary thickness is preferably 1 to 5 mm, the primary expansion ratio is 3 to 20 times, the cell diameter is 0.05 to 0.3 mm, and the closed cell ratio is preferably 70% or more. PPE3
0 to 65 parts by weight and the polystyrene component 35 to 70 parts by weight are more preferable, and PPE 35 to 60 parts by weight and the polystyrene component 40 to 65 parts by weight are even more preferable. The amount of volatile components remaining in the foamed sheet is 1 to 5 parts by weight,
It is preferably 2 to 4 parts by weight.
【0015】PPE系樹脂の混合重量部が小さいときは
耐熱性が劣る傾向があり、PPE系樹脂の混合重量部が
大きいときは加熱流動時の粘度が上昇し発泡成形が困難
になる場合がある。発泡シートの一次厚みが1mm未満
の場合、強度・断熱性に劣り自動車内装材用発泡積層シ
ートとして適当でない場合がある。また発泡シート一次
厚みが5mm以上の場合、成形加熱時に熱が変性発泡層
の厚み方向の中心部まで伝わり難く、そのため十分な加
熱が行えず成形性が悪くなる場合がある。また、十分な
加熱を行うべく加熱時間を長くすると、発泡層表面のセ
ルの破泡等が生じ、製品として許容できるものが得られ
難い。一次発泡倍率が3倍未満の場合、柔軟性に劣り曲
げ等による破損が生じ易く、また軽量なものが得られな
い。20倍以上の場合強度、成形性に劣る傾向がある。
セル径が0.05mm以下の場合強度が得られず、0.
3mm以上の場合、断熱性に劣る傾向がある。また、独
立気泡率が70%以下の場合、断熱性、剛性に劣るとと
もに成形加熱時の2次発泡倍率を得難くなり、成形性に
劣る傾向がある。When the mixed weight part of the PPE resin is small, the heat resistance tends to be inferior, and when the mixed weight part of the PPE resin is large, the viscosity at the time of heating and flowing may be increased to make foam molding difficult. . When the primary thickness of the foamed sheet is less than 1 mm, it may be unsuitable as a foamed laminated sheet for automobile interior materials due to poor strength and heat insulating properties. Further, when the primary thickness of the foamed sheet is 5 mm or more, it is difficult for heat to be transferred to the central portion in the thickness direction of the modified foamed layer at the time of molding heating, so that sufficient heating cannot be performed and moldability may deteriorate. Further, if the heating time is extended to perform sufficient heating, the cells on the surface of the foam layer will be broken, and it will be difficult to obtain an acceptable product. When the primary expansion ratio is less than 3 times, the flexibility is poor and damage due to bending is likely to occur, and a lightweight product cannot be obtained. When it is 20 times or more, the strength and moldability tend to be poor.
When the cell diameter is 0.05 mm or less, strength cannot be obtained, and
When it is 3 mm or more, the heat insulating property tends to be poor. Further, when the closed cell ratio is 70% or less, the heat insulating property and the rigidity are poor, and it becomes difficult to obtain the secondary expansion ratio at the time of molding and heating, and the moldability tends to be poor.
【0016】本発明における変性PPE系樹脂発泡層
に、非発泡層を積層する方法としては、あらかじめフィ
ルム状に成形した樹脂を発泡成形され供給される発泡層
の上面および/または下面に熱ロール等により接着する
方法、多層押出金型を用いて行う共押出積層方法等が挙
げられるが、あらかじめ発泡成形され、供給される発泡
層の上下面に押出機から供給される可塑化状態にある非
発泡層を冷却ローラーなどによって積層・固着する方法
が好ましい。中でも、発泡層の押出発泡シート成形と非
発泡層の押出をインライン中で行い積層する方法が特に
好ましい。As a method for laminating a non-foamed layer on the modified PPE resin foamed layer in the present invention, a resin which has been molded into a film shape in advance is foam-molded and supplied on the upper and / or lower surface of the foamed layer such as a heat roll. Examples of the method include a method of adhering by a method of coextrusion, a method of coextrusion lamination using a multi-layer extrusion die, and the like. A method of laminating and fixing the layers with a cooling roller or the like is preferable. Above all, a method of laminating by extruding a foamed layer into an extruded foam sheet and extruding a non-foamed layer in-line is particularly preferable.
【0017】非発泡層の熱可塑性樹脂として使用される
ものとしては、ポリスチレン系樹脂(PS系樹脂)、耐
熱ポリスチレン系樹脂(耐熱PS系樹脂)、変成PPE
系樹脂、ポリプロピレン(PP)系樹脂、ポリエチレン
(PE)系樹脂、ポリエチレンテレフタレート(PE
T)系樹脂、ポリアミド(ナイロン)系樹脂等が挙げら
れ、これらは単独又は2種以上の組み合わせて用いられ
るが、変成PPE系樹脂発泡層との接着性からPS系、
耐熱PS系、変成PPE系樹脂が好適である。耐熱PS
系樹脂としてはスチレンとカルボキシル基含有モノマー
との共重合体が挙げられ、例えばスチレン−無水マレイ
ン酸共重合体、スチレン−アクリル酸共重合体、スチレ
ン−メタクリル酸共重合体、スチレン−イタコン酸共重
合体やそれらの共重合体とポリスチレン、ポリカーボネ
ート、ポリフェニレンオキサイドなどの重合体とのブレ
ンド物が挙げられる。耐熱、剛性、発泡シートとの接着
性の点において、変成PPE系樹脂が特に好適である。Polystyrene resin (PS resin), heat-resistant polystyrene resin (heat-resistant PS resin), and modified PPE are used as the thermoplastic resin of the non-foamed layer.
Resin, polypropylene (PP) resin, polyethylene (PE) resin, polyethylene terephthalate (PE
T) -based resins, polyamide (nylon) -based resins, and the like, which may be used alone or in combination of two or more, and are PS-based, because of their adhesiveness to the modified PPE-based resin foam layer.
Heat-resistant PS-based and modified PPE-based resins are suitable. Heat resistant PS
Examples of the system resin include copolymers of styrene and a carboxyl group-containing monomer, for example, styrene-maleic anhydride copolymer, styrene-acrylic acid copolymer, styrene-methacrylic acid copolymer, styrene-itaconic acid copolymer. Examples thereof include blends of polymers and copolymers thereof with polymers such as polystyrene, polycarbonate, and polyphenylene oxide. The modified PPE resin is particularly preferable in terms of heat resistance, rigidity, and adhesiveness with the foamed sheet.
【0018】非発泡層に好適に使用される変成PPE系
樹脂としては、発泡層に用いいられる変性PPE樹脂と
同じく、PPE成分25〜70重量部とポリスチレン成
分75〜30重量部であるPPEとPSの混合樹脂及び
フェニルエーテルとスチレンとのグラフト共重合体、該
共重合体とPS系樹脂の混合樹脂等が挙げられるが、製
造が容易である点でPPEとPSの混合樹脂が好まし
い。As the modified PPE resin preferably used for the non-foamed layer, the same as the modified PPE resin used for the foamed layer, PPE containing 25 to 70 parts by weight of PPE component and 75 to 30 parts by weight of polystyrene component. Examples thereof include a mixed resin of PS, a graft copolymer of phenyl ether and styrene, a mixed resin of the copolymer and PS resin, and the like, and a mixed resin of PPE and PS is preferable in terms of easy production.
【0019】前記PPE系樹脂の具体例、好ましいも
の、PS系樹脂の具体例、好ましいもの、スチレン系単
量体の具体例、好ましいもの、さらには、PS系樹脂に
含まれるまたはスチレン系単量体と重合可能な単量体の
具体例などは、発泡層と同じであるので、説明は省略す
る。ただし、PS系樹脂の好ましい具体例として、ハイ
インパクトポリスチレン(HIPS)で代表されるスチ
レン−ブタジエン共重合体が、非発泡層の耐衝撃改善効
果が大きいという点から追加される。Specific examples and preferred examples of the PPE-based resin, specific examples and preferred examples of the PS-based resin, specific examples and preferred examples of the styrene-based monomer, and further, those contained in the PS-based resin or the styrene-based monomer. Specific examples of the monomer that can be polymerized with the body are the same as those of the foam layer, and thus the description thereof is omitted. However, a styrene-butadiene copolymer typified by high-impact polystyrene (HIPS) is added as a preferable specific example of the PS-based resin because the non-foamed layer has a large impact resistance improving effect.
【0020】変性PPE系樹脂のPPE成分の割合が2
5重量部以下と少なくなる場合には、成形体の耐熱性が
劣る傾向があり、変性PPE系樹脂のPPE成分の割合
が70重量部以上になる場合には、成形が困難となる傾
向がある。本発明における発泡積層シートにおいて、非
発泡層は発泡層の両面もしくは片面に積層されるが、製
造コストが安価で軽量な後者の方が好ましい。The ratio of PPE component of the modified PPE resin is 2
When the amount is less than 5 parts by weight, the heat resistance of the molded article tends to be poor, and when the ratio of the PPE component of the modified PPE resin is 70 parts by weight or more, the molding tends to be difficult. . In the foamed laminated sheet of the present invention, the non-foamed layer is laminated on both sides or one side of the foamed layer, but the latter, which is inexpensive in manufacturing cost and lightweight, is preferable.
【0021】本発明で非発泡層に混合される無機フィラ
ーには特に制限はなく、タルク(ケイ酸マグネシウ
ム)、炭酸カルシウム(重質、軽質、膠質等)、マイ
カ、酸化マグネシウム、炭酸マグネシウム、硫酸バリウ
ム、硫酸カルシウム、亜硫酸カルシウム、シリカ、クレ
ー、カオリン、ホワイトカーボン、水酸化マグネシウ
ム、カーボンブラック、ゼオライト、モリブデンが挙げ
られ、これらの中でも特にタルク、炭酸カルシウム、マ
イカが好ましい。無機フィラーの添加量は変性PPE樹
脂100重量部に対して1〜50重量部、好ましくは5
〜40重量部である。この添加量が1重量部未満では耐
熱性改善等の無機物を充填した明確な効果が得られず、
50重量部を越えて添加すると樹脂の粘度が増加し押出
機に大きな負荷がかかるため好ましくなく、また非発泡
層の衝撃強度の低下が著しくなる。The inorganic filler to be mixed in the non-foamed layer in the present invention is not particularly limited, and talc (magnesium silicate), calcium carbonate (heavy, light, colloidal, etc.), mica, magnesium oxide, magnesium carbonate, sulfuric acid. Examples thereof include barium, calcium sulfate, calcium sulfite, silica, clay, kaolin, white carbon, magnesium hydroxide, carbon black, zeolite and molybdenum, and among these, talc, calcium carbonate and mica are particularly preferable. The amount of the inorganic filler added is 1 to 50 parts by weight, preferably 5 parts by weight, based on 100 parts by weight of the modified PPE resin.
4040 parts by weight. If this addition amount is less than 1 part by weight, a clear effect of filling the inorganic material such as heat resistance cannot be obtained,
If it is added in excess of 50 parts by weight, the viscosity of the resin increases and a large load is applied to the extruder, which is not preferable, and the impact strength of the non-foamed layer is significantly reduced.
【0022】本発明において使用される非発泡層の熱可
塑性樹脂には、必要に応じて耐衝撃性改良剤、滑剤、酸
化防止剤、静電防止剤、顔料等を単独または2種類以上
組み合わせて添加することができる。前記耐衝撃改良剤
は、非発泡層を変性PPE系樹脂発泡層に積層し、2次
発泡させて成形した自動車内装材を輸送する際や、自動
車内装材にさらにパンチング加工を行う際に、非発泡層
の割れなどを防止するために使用されるもので、非発泡
層を形成する熱可塑性樹脂に混合して使用される。具体
的には、耐衝撃改良剤として、天然ゴムおよび合成ゴム
が用いられる。好適に使用しうるゴムまたはゴム状ポリ
マーとしては、たとえば天然クレープゴム、SBRタイ
プゴム、GR−Nタイプゴム、ブタジエンゴム、ブタジ
エン−スチレンゴムまたはイソプレンから製造される合
成ゴム、エラストマー性の改質ジエンポリマー、ポリブ
タジエンとスチレンのゴム状ポリマー等が挙げられる。
耐衝撃改良材の配合量としては、通常、非発泡層を構成
する熱可塑性樹脂中にゴム成分量として1〜15部含有
されるように配合されるのが好ましい。In the thermoplastic resin of the non-foamed layer used in the present invention, an impact resistance improver, a lubricant, an antioxidant, an antistatic agent, a pigment, etc. may be used alone or in combination of two or more kinds, if necessary. It can be added. The impact resistance improver is a non-foaming layer that is laminated on a modified PPE resin foam layer, and is used for transporting an automobile interior material molded by secondary foaming, or for further punching processing on the automobile interior material. It is used to prevent cracking of the foam layer, and is used by being mixed with the thermoplastic resin forming the non-foam layer. Specifically, natural rubber and synthetic rubber are used as the impact modifier. Suitable rubbers or rubbery polymers include, for example, natural crepe rubber, SBR type rubber, GR-N type rubber, butadiene rubber, butadiene-styrene rubber or synthetic rubber produced from isoprene, elastomeric modified dienes. Examples thereof include polymers and rubber-like polymers of polybutadiene and styrene.
The amount of the impact resistance improver to be added is generally preferably such that the thermoplastic resin forming the non-foamed layer contains 1 to 15 parts by weight of a rubber component.
【0023】ゴム成分を含有する変性PPE系樹脂中の
ゴム成分量を特定する方法としては、ゴム成分が不溶で
変性PPE系樹脂が溶解する溶媒に混合樹脂を溶かし、
不溶分を分離し重量を測定する方法(分別法)、IR等
で測定、定量する方法等がある。例えば、ゴム成分がS
BRの場合、トルエン溶媒にゴム入り変性PPEを溶か
し、不溶分の重量を測定することでゴム成分の重量比率
を算出する。As a method for specifying the amount of the rubber component in the modified PPE resin containing the rubber component, the mixed resin is dissolved in a solvent in which the rubber component is insoluble and the modified PPE resin is dissolved,
There are a method of separating the insoluble matter and measuring the weight (fractionation method), a method of measuring and quantifying by IR and the like. For example, the rubber component is S
In the case of BR, the modified PPE containing rubber is dissolved in a toluene solvent and the weight of the insoluble portion is measured to calculate the weight ratio of the rubber component.
【0024】本発明における発泡積層シートにおいて発
泡層に積層される非発泡層の厚みは50〜300μmが
好ましい。50μmより薄い場合には強度、剛性、耐熱
性等に劣り、300μmより厚い場合には成形性に劣
る。本発明において用いられる変性PPE系樹脂発泡積
層シートには、従来の自動車内装材として用いられる表
皮材、例えば織布、不織布、発泡層等を必要に応じて積
層することができる。表皮材の基材としては、ポリエチ
レンテレフタレート、ポリプロピレン、ポリアミド、ポ
リアクリロニトリル、ナイロン等の合成樹脂や羊毛、木
綿等の天然素材を使用することができ、それらを組み合
わせても良い。In the foam laminated sheet of the present invention, the thickness of the non-foam layer laminated on the foam layer is preferably 50 to 300 μm. When the thickness is less than 50 μm, the strength, rigidity, heat resistance and the like are poor, and when the thickness is more than 300 μm, the moldability is poor. The modified PPE resin foam laminated sheet used in the present invention can be laminated with a skin material used as a conventional automobile interior material, for example, a woven fabric, a non-woven fabric, a foam layer or the like, if necessary. As the base material of the skin material, synthetic resins such as polyethylene terephthalate, polypropylene, polyamide, polyacrylonitrile and nylon, and natural materials such as wool and cotton can be used, and they may be combined.
【0025】本発明において用いられる変性PPE系樹
脂発泡積層シートに表皮材を接着する方法としては接着
剤を介して発泡積層シートに接着する方法等が挙げられ
る。接着剤としては、熱可塑性接着剤、ホットメルト接
着剤、ゴム系接着剤、熱硬化性接着剤、モノマー反応型
接着剤、無機系接着剤、天然物接着剤等が挙げられる
が、接着が容易な点でホットメルト接着剤が好適であ
る。ホットメルト接着剤としては、オレフィン系、変性
オレフィン系、ポリウレタン系、エチレン・酢酸ビニル
共重合樹脂系、ポリアミド系、ポリエステル系、熱可塑
性ゴム系、スチレン−ブタン共重合体、スチレン−イソ
プレン共重合体系樹脂を成分としたものが挙げらる。Examples of the method for adhering the skin material to the modified PPE resin foam laminated sheet used in the present invention include a method for adhering it to the foam laminated sheet via an adhesive. Examples of adhesives include thermoplastic adhesives, hot melt adhesives, rubber adhesives, thermosetting adhesives, monomer-reactive adhesives, inorganic adhesives, natural adhesives, etc. Hot melt adhesives are suitable in this respect. Hot melt adhesives include olefin-based, modified olefin-based, polyurethane-based, ethylene / vinyl acetate copolymer resin-based, polyamide-based, polyester-based, thermoplastic rubber-based, styrene-butane copolymer, styrene-isoprene copolymer-based An example of which is a resin.
【0026】表皮材の接着方法としては、あらかじめ表
皮材に接着剤が接着してあるものを発泡積層シートに熱
ロール等を用いて接着する方法あるいは発泡積層シート
に仮止めし加熱成型時に成形と接着を同時に行う方法、
接着剤を発泡積層シートにバインダーラミネーション法
やあらかじめフィルム状に成形された接着剤を熱ラミネ
ーション法等により積層した発泡積層シートに表皮材を
熱ロール等を用いて接着する方法あるいは表皮材を仮止
めし加熱成型時に成形と接着を同時に行う方法、接着剤
を発泡積層シートに積層する際に表皮材を同時に接着す
る方法等が挙げられる。As a method for adhering the skin material, a method in which an adhesive is preliminarily adhered to the skin material is adhered to the foamed laminated sheet using a heat roll or the like, or it is temporarily fixed to the foamed laminated sheet and molded during heat molding. A method of bonding at the same time,
A method of adhering the skin material to the foam laminated sheet using a heat roll or the like, or temporarily fixing the skin material to the foam laminated sheet in which the adhesive is laminated on the foam laminated sheet by the binder lamination method or the adhesive formed in advance in a film shape by the heat lamination method. Then, a method of simultaneously performing molding and adhesion at the time of heat-molding, a method of simultaneously adhering a skin material when laminating an adhesive on a foam laminated sheet, and the like can be mentioned.
【0027】本発明による自動車内装材用発泡積層シー
トの成形方法としては、上下にヒーターを持つ加熱炉の
中央に積層シートをクランプして導き、成形に適した温
度に加熱し二次発泡させた後、温度調節をした金型にて
真空成形・圧空成形等やフリードローイング成形、プラ
グ・アンド・リッジ成形、リッジ成形、マッチド・モー
ルド成形、ストレート成形、ドレープ成形、リバースド
ロー成形、エアスリップ成形、プラグアシスト成形、プ
ラグアシストリバースドロー成形等にて成形する方法が
挙げられる。また、成形の際の発泡層の二次発泡によ
り、二次厚み2.0〜10mmとなるようにすることが
望ましい。As a method for molding a foamed laminated sheet for automobile interior materials according to the present invention, the laminated sheet is guided by clamping it in the center of a heating furnace having heaters above and below, and heated to a temperature suitable for molding to carry out secondary foaming. After that, vacuum molding, pressure molding, free drawing molding, plug and ridge molding, ridge molding, matched mold molding, straight molding, drape molding, reverse draw molding, air slip molding, etc. Examples of the molding method include plug-assist molding and plug-assist reverse draw molding. In addition, it is desirable that the secondary thickness of the foamed layer is 2.0 to 10 mm due to secondary foaming of the foamed layer during molding.
【0028】本発明による自動車内装材用発泡積層シー
トを自動車に固定する場合の配置としては、無機フィラ
ーを含む非発泡層を、図1に示すように、発泡層の上面
(天井外板車内面側)に配置することが高温時の強度の
点から望ましい。When the foamed laminated sheet for automobile interior materials according to the present invention is fixed to an automobile, a non-foamed layer containing an inorganic filler is used as shown in FIG. It is desirable to arrange it on the side) from the viewpoint of strength at high temperature.
【0029】[0029]
【作用】本発明の、少なくとも片面に無機フィラーを充
填した非発泡層を設けることで耐熱性が改善された自動
車内装材用発泡積層シートは、高温下におけるヒートサ
グの改善だけでなく軽量かつ安価であり、従来にない品
質及びコスト競争力に優れたものである。The foamed laminated sheet for automobile interior materials, which has improved heat resistance by providing a non-foamed layer having at least one surface filled with an inorganic filler, is not only improved in heat sag at high temperatures but also lightweight and inexpensive. It has excellent quality and cost competitiveness that have never existed before.
【0030】[0030]
【実施例】以下に本発明の実施例について説明する。な
お、本発明はこれらにより何ら制限を受けるものではな
い。実施例・比較例に用いた樹脂を表1に、充填剤を表
2に、その他の材料を表3に示す。Embodiments of the present invention will be described below. The present invention is not limited by these. Table 1 shows resins used in Examples and Comparative Examples, Table 2 shows fillers, and Table 3 shows other materials.
【0031】[0031]
【表1】 [Table 1]
【0032】[0032]
【表2】 [Table 2]
【0033】[0033]
【表3】 [Table 3]
【0034】発泡積層シートの成形体の耐熱性試験に関
して、以下の方法でヒートサグ試験(片持ち耐熱試験)
を行った。成形体の一部分を試験片として225mm
(発泡積層シートの押出MD方向)×25mm(発泡積
層シートの幅TD方向)の寸法で切り出し、試験片の一
方の端部25mmを保持具にクランプし、片方は自由の
状態にして200mmオーバーハングさせた。自由端上
面に測定点を刻印し更に自由端から5mmの位置に5g
の分銅をのせ荷重をかけた。試験片自由端の垂れ下がり
を測定するために標線を設け、加熱前に標線と測定点の
距離を測定した。次に試験片保持具を85±1℃に設定
した恒温槽内に2時間投入した。その後、試験片保持具
を恒温槽から取り出し、加熱後の試験片の測定点と標線
の距離を測定し、試験片先端の垂れ下がり量を算出し
た。Regarding the heat resistance test of the molded product of the foamed laminated sheet, the heat sag test (cantilever heat resistance test) is carried out by the following method.
Was done. 225 mm with a part of the molded body as a test piece
Cut out in a dimension of (extruded MD direction of foamed laminated sheet) × 25 mm (width TD direction of foamed laminated sheet), clamp one end 25 mm of the test piece to a holder, and leave one side in a free state and overhang it by 200 mm Let Mark the measurement point on the upper surface of the free end and add 5g to the position 5mm from the free end.
A weight was put on and a load was applied. A marked line was provided to measure the sag of the free end of the test piece, and the distance between the marked line and the measurement point was measured before heating. Next, the test piece holder was placed in a constant temperature bath set at 85 ± 1 ° C. for 2 hours. Then, the test piece holder was taken out from the constant temperature bath, the distance between the measurement point of the heated test piece and the marked line was measured, and the amount of sagging of the tip of the test piece was calculated.
【0035】評価基準は次の通りである。 ◎:試験片の垂れ下がりが5mm未満である。 ○:試験片の垂れ下がりが5mm以上、10mm未満で
ある。 ×:試験片の垂れ下がりが10mm以上である。 (一次発泡倍率、平均セル径、独立気泡率) 一次発泡倍率:発泡シートの密度dfをJIS K72
22に準じて測定し、変性PPE樹脂の密度dpをJI
S K7112に準じて測定した。 一次発泡倍率=df/dp 平均セル径:発泡シートの断面を光学顕微鏡、電子顕微
鏡で観察し、任意のn=20以上のセル径を測定し平均
して算出した。 独立気泡率:発泡シートをASTM D−2856に準
じて測定した(マルチビクノメーター(ベックマン社
製)を使用)。The evaluation criteria are as follows. A: The sagging of the test piece is less than 5 mm. ◯: The sagging of the test piece is 5 mm or more and less than 10 mm. X: The sagging of the test piece is 10 mm or more. (Primary expansion ratio, average cell diameter, closed cell ratio) Primary expansion ratio: The density df of the foamed sheet is defined by JIS K72.
22 to measure the density dp of the modified PPE resin according to JI
It was measured according to SK7112. Primary expansion ratio = df / dp Average cell diameter: The cross section of the foamed sheet was observed with an optical microscope and an electron microscope, and an arbitrary n = 20 or more cell diameter was measured and averaged to calculate. Closed cell ratio: The foamed sheet was measured according to ASTM D-2856 (using a multi-vicnometer (manufactured by Beckman)).
【0036】[0036]
【実施例1】PPE樹脂成分40重量%、PS樹脂成分
60重量%となるように、PPE樹脂(A)とPS樹脂
(C)とを混合した混合樹脂100重量部に対して、i
so−ブタンを主成分とする発泡剤(iso/n=85
/15)3重量部、およびタルク0.32重量部を押出
機により加熱混練し、樹脂温度198℃まで冷却し、サ
ーキュラーダイスにより押出し、一次厚み2.6mm、
一次発泡倍率10倍、独立気泡率85%、平均セル径
0.19mm、目付け240g/m2の発泡層を得た。
得られたシートはロール状に巻き取られた。Example 1 For 100 parts by weight of a mixed resin in which PPE resin (A) and PS resin (C) were mixed so that the PPE resin component was 40% by weight and the PS resin component was 60% by weight, i
A foaming agent containing so-butane as a main component (iso / n = 85
/ 15) 3 parts by weight and 0.32 parts by weight of talc are kneaded by heating with an extruder, cooled to a resin temperature of 198 ° C., and extruded with a circular die to have a primary thickness of 2.6 mm,
A primary foaming ratio of 10 times, a closed cell rate of 85%, an average cell diameter of 0.19 mm, and a basis weight of 240 g / m 2 were obtained as a foamed layer.
The obtained sheet was wound into a roll.
【0037】得られたシートを繰り出し、PPE樹脂成
分30重量%,PS樹脂成分64重量%,ゴム成分6重
量%となるようにPPE樹脂(B)、PS樹脂(C)お
よび耐衝撃性改良剤(D)を混合した混合樹脂100重
量部に対してタルク(E)10重量部を加えたものを溶
融・混練しTダイを用いて樹脂温度278℃で押出し、
発泡層の片面に厚み150μmの非発泡層を積層した。
得られた積層シートはロール状に巻取られた。 次に、
非発泡層と異なる側の発泡層表面にホットメルトフィル
ム接着剤(H)を介して表皮材(I)と重ね合わせたも
のを仮止めした。表皮材とホットメルトフィルム接着剤
を仮止めした発泡積層シートの四方をクランプし加熱炉
にいれ表面温度155℃まで加熱し、60℃に温調した
金型にてプラグ成形を行った結果、強固に接着、積層さ
れた自動車内装材用発泡積層体が得られた。このもの
を、トリミング、パンチング加工を施し自動車内装材用
発泡積層成形体を得た。The obtained sheet was fed out, and the PPE resin (B), PS resin (C) and impact resistance improver were adjusted so that the PPE resin component was 30% by weight, the PS resin component was 64% by weight, and the rubber component was 6% by weight. A mixture of 100 parts by weight of (D) and 10 parts by weight of talc (E) was melted and kneaded and extruded at a resin temperature of 278 ° C. using a T-die.
A non-foamed layer having a thickness of 150 μm was laminated on one side of the foamed layer.
The obtained laminated sheet was wound into a roll. next,
The surface of the foamed layer on the side different from the non-foamed layer was temporarily fixed to the surface of the foamed layer (I) with the hot melt film adhesive (H) interposed therebetween. Clamping the four sides of the foamed laminated sheet where the skin material and the hot melt film adhesive were temporarily fixed, put it in a heating furnace and heat it to a surface temperature of 155 ° C, and perform plug molding with a mold whose temperature was adjusted to 60 ° C. A foam laminate for an automobile interior material, which was adhered to and laminated on the above, was obtained. This product was subjected to trimming and punching processing to obtain a foam laminated molding for automobile interior materials.
【0038】得られた自動車内装材用発泡積層体より試
験片を切り出し、非発泡層を上面にしてヒートサグ試験
をおこなったところ、試験片の垂れ下がりは殆どなかっ
た。得られた自動車内装材用発泡積層体の非発泡層の含
有無機フィラー種、耐熱試験時の非発泡層の配置、ヒー
トサグ試験結果を表4に示す。A test piece was cut out from the obtained foam laminate for automobile interior material and subjected to a heat sag test with the non-foamed layer as the upper surface. As a result, there was almost no sagging of the test piece. Table 4 shows the inorganic filler species contained in the non-foamed layer of the foamed laminate for automobile interior materials, the arrangement of the non-foamed layer during the heat resistance test, and the heat sag test result.
【0039】[0039]
【実施例2】無機フィラーとしてタルク(E)の代わり
に炭酸カルシウム(F)を20重量部使用した以外は、
実施例1記載の方法と同様の方法により自動車内装材用
発泡積層体を得た。得られた自動車内装材用発泡積層体
より試験片を切り出し、非発泡層を上面にしてヒートサ
グ試験をおこなったところ、試験片の垂れ下がりは殆ど
なかった。得られた自動車内装材用発泡積層体の非発泡
層の含有無機フィラー種、耐熱試験時の非発泡層の配
置、ヒートサグ試験結果を表4に示す。Example 2 Except that 20 parts by weight of calcium carbonate (F) was used instead of talc (E) as the inorganic filler.
A foam laminate for an automobile interior material was obtained by the same method as described in Example 1. When a test piece was cut out from the obtained foam laminate for automobile interior material and subjected to a heat sag test with the non-foamed layer as the upper surface, almost no sagging of the test piece occurred. Table 4 shows the inorganic filler species contained in the non-foamed layer of the foamed laminate for automobile interior materials, the arrangement of the non-foamed layer during the heat resistance test, and the heat sag test result.
【0040】[0040]
【実施例3】無機フィラーとしてタルク(E)の代わり
にマイカ(G)を10重量部使用した以外は、実施例1
記載の方法と同様の方法により自動車内装材用発泡積層
体を得た。得られた自動車内装材用発泡積層体より試験
片を切り出し、非発泡層を上面にしてヒートサグ試験を
おこなったところ、試験片の垂れ下がりは殆どなかっ
た。得られた自動車内装材用発泡積層体の非発泡層の含
有無機フィラー種、耐熱試験時の非発泡層の配置、ヒー
トサグ試験結果を表4に示す。[Example 3] Example 1 except that 10 parts by weight of mica (G) was used instead of talc (E) as an inorganic filler.
A foam laminate for an automobile interior material was obtained by the same method as described. When a test piece was cut out from the obtained foam laminate for automobile interior material and subjected to a heat sag test with the non-foamed layer as the upper surface, almost no sagging of the test piece occurred. Table 4 shows the inorganic filler species contained in the non-foamed layer of the foamed laminate for automobile interior materials, the arrangement of the non-foamed layer during the heat resistance test, and the heat sag test result.
【0041】[0041]
【実施例4】非発泡層側にホットメルトフィルム接着剤
(H)を介して表皮材(I)と重ね合わせたものを仮止
めした以外は、実施例1記載の方法と同様の方法により
自動車内装材用発泡積層体を得た。得られた自動車内装
材用発泡積層体より試験片を切り出し、非発泡層を下面
(表皮材を下)にして、ヒートサグ試験をおこなったと
ころ、試験片に若干の垂れが観測された。得られた自動
車内装材用発泡積層体の非発泡層の含有無機フィラー
種、耐熱試験時の非発泡層の配置、片持ち耐熱試験結果
を表4に示す。[Example 4] An automobile was manufactured by the same method as that described in Example 1 except that the non-foamed layer side, which was laminated with the skin material (I) via the hot melt film adhesive (H), was temporarily fixed. A foam laminate for an interior material was obtained. A test piece was cut out from the obtained foam laminate for an automobile interior material, and a non-foamed layer was placed on the lower surface (the skin material was facing down), and a heat sag test was carried out. As a result, some sagging was observed on the test piece. Table 4 shows the types of inorganic fillers contained in the non-foamed layer of the foam laminate for automobile interior materials, the arrangement of the non-foamed layer during the heat resistance test, and the cantilever heat resistance test results.
【0042】[0042]
【比較例1】無機フィラーを使用しなかった以外は、実
施例1記載の方法と同様の方法により自動車内装材用発
泡積層体を得た。得られた自動車内装材用発泡積層体よ
り試験片を切り出し、非発泡層を上面にしてヒートサグ
試験をおこなったところ、試験片の垂れ下がりが観察さ
れた。得られた自動車内装材用発泡積層体の非発泡層の
含有無機フィラー種、耐熱試験時の非発泡層の配置、片
持ち耐熱試験結果を表4に示す。Comparative Example 1 A foam laminate for an automobile interior material was obtained by the same method as that described in Example 1 except that the inorganic filler was not used. A test piece was cut out from the obtained foam laminate for an automobile interior material and subjected to a heat sag test with the non-foamed layer as an upper surface. As a result, sagging of the test piece was observed. Table 4 shows the types of inorganic fillers contained in the non-foamed layer of the foam laminate for automobile interior materials, the arrangement of the non-foamed layer during the heat resistance test, and the cantilever heat resistance test results.
【0043】[0043]
【表4】 [Table 4]
【0044】上記のように実施例1〜4に示した無機フ
ィラーを含む非発泡層を有する発泡積層シートは、比較
例1の無機フィラーを含まない非発泡層を有する発泡積
層シートと比較し、耐熱性に非常に優れた効果を示すこ
とが分かる。また、実施例1、2、3と実施例4と比較
すると、発泡積層シートを固定する際には上面に非発泡
層を設けることで耐熱性に優れた効果を示すことが分か
る。The foamed laminated sheet having the non-foamed layer containing the inorganic filler shown in Examples 1 to 4 as described above is compared with the foamed laminated sheet having the non-foamed layer not containing the inorganic filler of Comparative Example 1, It can be seen that it has a very excellent effect on heat resistance. Further, comparing Examples 1, 2, 3 and Example 4, it can be seen that the effect of excellent heat resistance is exhibited by providing the non-foaming layer on the upper surface when fixing the foamed laminated sheet.
【0045】[0045]
【発明の効果】上述のとおり、本発明の少なくとも片面
非発泡層に無機フィラーを含む自動車内装材用発泡積層
シートを用いれば、従来の無機質のガラス繊維をベース
とした基材の軽量化、コスト高の問題の改善された、更
に品質の優れた自動車内装材用発泡積層シートが提供さ
れる。As described above, the use of the foamed laminated sheet for automobile interior materials containing the inorganic filler in at least one non-foamed layer of the present invention reduces the weight and cost of the conventional inorganic glass fiber-based substrate. Provided is a foamed laminated sheet for automobile interior material, which is improved in the problem of height and has excellent quality.
【図1】本発明の自動車内装材用発泡積層シートの自動
車天井部における配置の例を示す。FIG. 1 shows an example of an arrangement of a foam laminated sheet for an automobile interior material of the present invention in an automobile ceiling portion.
1 天井外板 2 自動車天井基材 3 発泡層 4 フィラー含有非発泡層 1 Ceiling outer plate 2 Automotive ceiling base material 3 Foam layer 4 Non-foam layer containing filler
Claims (7)
層の少なくとも片面に無機フィラーを含む熱可塑性樹脂
からなる非発泡層を積層した自動車内装材用発泡積層シ
ート。1. A foamed laminated sheet for automobile interior materials, wherein a non-foamed layer made of a thermoplastic resin containing an inorganic filler is laminated on at least one side of a modified polyphenylene ether resin foamed layer.
対し、1〜50重量部の無機フィラーを含有せしめた樹
脂からなる請求項1記載の自動車内装材用発泡積層シー
ト。2. The foamed laminated sheet for automobile interior materials according to claim 1, wherein the non-foamed layer is made of a resin containing 1 to 50 parts by weight of an inorganic filler with respect to 100 parts by weight of the thermoplastic resin.
ムまたはマイカから選ばれる少なくとも1種である請求
項1または2記載の自動車内装材用発泡積層シート。3. The foamed laminated sheet for automobile interior materials according to claim 1 or 2, wherein the inorganic filler is at least one selected from talc, calcium carbonate and mica.
は変性ポリフェニレンエーテル系樹脂である請求項1、
2または3記載の自動車内装材用発泡積層シート。4. The non-foamed layer is a heat-resistant polystyrene resin or a modified polyphenylene ether resin.
The foamed laminated sheet for an automobile interior material according to 2 or 3.
として1〜15重量%含有する請求項4記載の自動車内
装材用発泡積層シート。5. The foamed laminated sheet for automobile interior materials according to claim 4, wherein the non-foamed layer contains an impact resistance improver as a rubber component in an amount of 1 to 15% by weight.
5〜70重量部とポリスチレン成分30〜75重量部で
あるポリフェニレンエーテル系樹脂とポリスチレン系樹
脂の混合樹脂、フェニルエーテルとスチレンとのグラフ
ト共重合樹脂、または該共重合樹脂とポリスチレン系樹
脂との混合樹脂からなる変性ポリフェニレンエーテル系
樹脂を基材樹脂とし、該基材樹脂に発泡剤を添加し押出
発泡させて得られる一次厚みが1〜5mm、一次発泡倍
率が3〜20倍、平均セル径が0.05〜0.3mm、
独立気泡率が70%以上の発泡層である請求項1、2、
3、4または5記載の自動車内装材用発泡積層シート。6. The foam layer comprises a polyphenylene ether component 2
5 to 70 parts by weight and 30 to 75 parts by weight of polystyrene component, mixed resin of polyphenylene ether resin and polystyrene resin, graft copolymer resin of phenyl ether and styrene, or mixture of copolymer resin and polystyrene resin. A modified polyphenylene ether-based resin made of a resin is used as a base resin, and a primary thickness obtained by adding a foaming agent to the base resin and performing extrusion foaming is 1 to 5 mm, a primary expansion ratio is 3 to 20 times, and an average cell diameter is 0.05-0.3 mm,
The foamed layer having a closed cell rate of 70% or more,
The foamed laminated sheet for automobile interior materials according to 3, 4, or 5.
上面に設置した請求項1、2、3、4、5または6記載
の自動車内装材用発泡積層シート。7. The foam laminated sheet for an automobile interior material according to claim 1, 2, 3, 4, 5, or 6, wherein a non-foam layer containing an inorganic filler is provided on the upper surface of the foam layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8035016A JPH09226034A (en) | 1996-02-22 | 1996-02-22 | Foamed laminated sheet for automobile interior material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8035016A JPH09226034A (en) | 1996-02-22 | 1996-02-22 | Foamed laminated sheet for automobile interior material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH09226034A true JPH09226034A (en) | 1997-09-02 |
Family
ID=12430282
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8035016A Pending JPH09226034A (en) | 1996-02-22 | 1996-02-22 | Foamed laminated sheet for automobile interior material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH09226034A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0988965A3 (en) * | 1998-09-26 | 2000-11-22 | Premark RWP Holdings, Inc. | Polymeric foam compositions and method of making substrates made from such compositions and method of making products made from such substrates and method of making |
SG83691A1 (en) * | 1997-11-25 | 2001-10-16 | Premark Rwp Holdings Inc | Polymeric foam substrate and its use as in combination with decorative surfaces |
JP2019097284A (en) * | 2017-11-21 | 2019-06-20 | 古河電気工業株式会社 | Exterior body for wire, and wire harness with exterior body |
-
1996
- 1996-02-22 JP JP8035016A patent/JPH09226034A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG83691A1 (en) * | 1997-11-25 | 2001-10-16 | Premark Rwp Holdings Inc | Polymeric foam substrate and its use as in combination with decorative surfaces |
EP0988965A3 (en) * | 1998-09-26 | 2000-11-22 | Premark RWP Holdings, Inc. | Polymeric foam compositions and method of making substrates made from such compositions and method of making products made from such substrates and method of making |
JP2019097284A (en) * | 2017-11-21 | 2019-06-20 | 古河電気工業株式会社 | Exterior body for wire, and wire harness with exterior body |
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