JP2899675B2 - Polypropylene resin for pasting synthetic type and pasting synthetic type method - Google Patents

Polypropylene resin for pasting synthetic type and pasting synthetic type method

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Publication number
JP2899675B2
JP2899675B2 JP63233333A JP23333388A JP2899675B2 JP 2899675 B2 JP2899675 B2 JP 2899675B2 JP 63233333 A JP63233333 A JP 63233333A JP 23333388 A JP23333388 A JP 23333388A JP 2899675 B2 JP2899675 B2 JP 2899675B2
Authority
JP
Japan
Prior art keywords
resin
mold
skin material
molding
polypropylene resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP63233333A
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Japanese (ja)
Other versions
JPH0280218A (en
Inventor
捷平 桝井
孚尚 原
正人 松本
信裕 臼井
重義 松原
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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Filing date
Publication date
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP63233333A priority Critical patent/JP2899675B2/en
Publication of JPH0280218A publication Critical patent/JPH0280218A/en
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Publication of JP2899675B2 publication Critical patent/JP2899675B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は自動車用内装部品等に使用する貼合成形品用
樹脂材料及び貼合成形方法に関する。詳しくは成形後に
優れた表皮材の風合いを保持できる同時賦形、貼合成形
用ポリプロピレン樹脂及びその貼合成形方法に関する。
Description: TECHNICAL FIELD The present invention relates to a resin material for a laminated synthetic product used for interior parts for automobiles and the like, and a method of laminating a synthetic resin. More specifically, the present invention relates to a polypropylene resin for simultaneous shaping and laminating, and a laminating method for laminating the same, which can maintain excellent texture of the skin material after molding.

(従来の技術) 最近の自動車の内装材、ドアトリム、クオータートリ
ム等のトリム類、インストルメンタルパネル各種ピラー
類として使用される表皮材と芯材樹脂との貼合成形品
は、外観的に高級感があり、風合いもよいものがますま
す要求されるようになってきている。これらの貼合成形
品の製造法として表皮材を芯材上に接着剤を用いて手貼
りする方法の他に、表皮材と芯材樹脂を同一金型内で賦
形と同時に一体貼合成形する方法がおこなわれている。
この同時賦形貼合成形プロセスとしては、表皮材を装着
した金型を閉じた状態で可塑化した樹脂を型内へ射出
し、賦形と貼合を同時におこなう方法、又は表皮材を装
着した金型を開いた状態で可塑化した樹脂を型内へ供給
しながら又は供給した後に金型を閉じ、賦形と貼合を同
時におこなう方法がある。従来これらの同時賦形、貼合
成形に用いられるポリプロピレンは一般射出成形用で、
JISK6758に準じ、温度230℃、荷重2.16kgの条件で測定
したメルトフローインデックス(以下、「MFI」ともい
う)が0.01〜100g/10分の流動性の範囲のものであっ
た。
(Prior art) In recent automobile interior materials, door trims, quarter trims and other trims, as well as skins and core materials used as various types of instrument panel pillars, synthetic composite products of appearance and luxurious appearance. There is an increasing demand for good texture. As a method of manufacturing these laminated synthetic products, in addition to a method of manually applying a skin material to a core material using an adhesive, the skin material and the core material resin are formed in the same mold and simultaneously integrally molded. There is a way to do that.
As the simultaneous shaping and laminating process, the plasticized resin is injected into the mold with the mold with the skin material closed, and the shaping and laminating are performed simultaneously, or the skin material is mounted. There is a method in which the mold is closed while supplying or after supplying the plasticized resin into the mold with the mold opened, and shaping and bonding are performed simultaneously. Conventionally, these simultaneous shaping, the polypropylene used for the pasting synthetic type is for general injection molding,
According to JISK6758, the melt flow index (hereinafter, also referred to as “MFI”) measured at a temperature of 230 ° C. and a load of 2.16 kg was within a fluidity range of 0.01 to 100 g / 10 minutes.

(発明が解決しようとする課題) しかしながら、同時賦形貼合成形に従来のポリプロピ
レン樹脂を使用すると成形品の風合いがそこなわれるこ
とがある。この様な成形方法では正確なデザインの転
写、表皮材と樹脂芯材との良好な接着性を得るために樹
脂温度は200〜250℃、樹脂の供給又は型締の圧力は50〜
1,000kg/cm2が必要である。すなわち、樹脂が金型内を
流れる際、高温の樹脂の熱は表皮に伝わり、表皮自体が
高温となる。又樹脂の流動時に高い剪断応力が発生し、
樹脂を金型の全面に均一な厚みで押し広げるために高い
圧力を必要とする。一方、表皮材としては、主として熱
可塑性樹脂系のものが使用されるため、高温高圧下で成
形すると永久変形を生じることが多い。この変形は具体
的に表皮材のシボ流れ、毛だおれ、発泡体のつぶれなど
となってあらわれ、貼合成形品の風合いが著しく低下す
る。これまで同時賦形貼合成形における表皮材の風合い
改良に関しては各種の方法が考案されている。例えば金
型の表皮に接する側の表面に模様づけしてシボ流れを防
ぐ方法(特開昭59−83633、特開昭60−212343)、表皮
材の裏うち層を改良してクッション性を維持する方法
(特開昭59−159342、特開昭60−212342、特開昭61−13
9425)等があるが風合い低下の原因となる高温、高圧の
成形条件の変更に関するものでなく、根本的な対策とな
っていないため風合いの著しい改良は困難であった。
(Problems to be Solved by the Invention) However, when a conventional polypropylene resin is used for the simultaneous imprinting and laminating type, the texture of a molded product may be deteriorated. In such a molding method, the resin temperature is 200 to 250 ° C., and the resin supply or mold clamping pressure is 50 to
1,000 kg / cm 2 is required. That is, when the resin flows through the mold, the heat of the high-temperature resin is transmitted to the skin, and the skin itself becomes hot. Also, high shear stress occurs when the resin flows,
High pressure is required to spread the resin over the entire surface of the mold with a uniform thickness. On the other hand, since a thermoplastic resin material is mainly used as the skin material, permanent deformation often occurs when molded under high temperature and high pressure. This deformation specifically appears as a textured flow of the skin material, hair frays, crushing of the foam, and the like, and the texture of the laminated synthetic product is significantly reduced. Until now, various methods have been devised for improving the texture of the skin material in the simultaneous shaping and laminating type. For example, a method of patterning the surface of the mold in contact with the skin to prevent grain flow (JP-A-59-83633, JP-A-60-212343), maintaining the cushioning property by improving the back layer of the skin material (JP-A-59-159342, JP-A-60-212342, JP-A-61-13)
9425), but it is not related to the change of high-temperature and high-pressure molding conditions that cause the texture to deteriorate, and it is difficult to significantly improve the texture because it is not a fundamental measure.

(課題を解決するための手段) 本願発明者らは金型内における同時賦形貼合成形法で
風合い低下を著しく少なくする成形材料の開発につき鋭
意研究した結果、以下に述べる発明に至った。まず成形
時の風合いの低下する原因を検討したところ熱、圧力、
延伸によることが明らかとなった。特にこれらの因子が
同時にはたらくと風合いは相乗的に低下することが判明
した。本願発明者らは芯材用の樹脂材料の側から成形時
に発生する、熱、圧力、延伸を低減すべく検討の結果、
一般に成形用として知られているよりきわめて流動性の
大きい、すなわちメルトフローインデックス120〜800g/
10分の流動性をもつポリプロピレン樹脂を芯材樹脂とし
て用いると表皮貼合成形品の表皮材の風合い低下が著し
く少なくなることを見出した。
(Means for Solving the Problems) The inventors of the present application have conducted intensive studies on the development of a molding material that significantly reduces the reduction in texture by the simultaneous shaping and laminating method in a mold, and as a result, have reached the invention described below. First, we examined the causes of the reduction in the texture during molding.
It became clear that it was due to stretching. In particular, it has been found that when these factors work simultaneously, the texture decreases synergistically. The present inventors have studied to reduce heat, pressure, and stretching generated during molding from the resin material side for the core material,
Extremely high fluidity than generally known for molding, i.e., a melt flow index of 120 to 800 g /
It has been found that when a polypropylene resin having a fluidity of 10 minutes is used as the core resin, the texture of the skin material of the skin-pasted synthetic product is significantly reduced.

この発明におけるポリプロピレン樹脂はプロピレンの
ホモポリマー、もしくはプロピレンとエチレンおよび/
又はブテンとのコポリマーであり、メルトフローインデ
ックスが120〜800g/分の流動性を有するものである。メ
ルトフローインデックス120g/10分より小さいと、成形
時の樹脂の流動時の剪断応力が大きいため高い成形圧力
が必要となる。メルトフローインデックスが800g/10分
より大きいと、ポリマーの機械的物性、特に衝撃強度が
表皮材と複合した状態でも実用に耐えないほど低下す
る。
The polypropylene resin in the present invention is a homopolymer of propylene or propylene and ethylene and / or
Or a copolymer with butene having a fluidity with a melt flow index of 120 to 800 g / min. If the melt flow index is less than 120 g / 10 minutes, a high molding pressure is required because the shear stress during the flow of the resin during molding is large. If the melt flow index is more than 800 g / 10 minutes, the mechanical properties of the polymer, particularly the impact strength, are so low that they cannot be put to practical use even in the state of being combined with the skin material.

高流動化したポリプロピレン樹脂を得る方法として、
重合で分子量を制御して製造する方法がある。又、重合
後に有機過酸化物又は熱で分解により分子量低下して製
造する方法もあり、有機過酸化物としては2,5−ジメチ
ル−2,5−tブチルパーオキシヘキサン、2,5−ジメチル
−2,5−tブチルパーオキシヘキセン−8などのジアル
キルパーオキサイド類、2,5−ジメチルヘキサン−2,5−
ジハイドロパーオキサイド、p−メンタンハイドロパー
オキサイド類及びケトンパーオキサイド類、パーオキシ
エステル類の中で100℃における半減期が10時間をこえ
るものが適当である。
As a method to obtain a highly fluidized polypropylene resin,
There is a method of producing by controlling the molecular weight by polymerization. Further, there is also a method of producing by reducing the molecular weight by decomposition with an organic peroxide or heat after polymerization, and as the organic peroxide, 2,5-dimethyl-2,5-tbutylperoxyhexane, 2,5-dimethyl Dialkyl peroxides such as -2,5-tbutylperoxyhexene-8, 2,5-dimethylhexane-2,5-
Among dihydroperoxides, p-menthane hydroperoxides, ketone peroxides and peroxyesters, those having a half-life at 100 ° C. of more than 10 hours are suitable.

該ポリプロピレン樹脂には酸化防止剤、紫外線防止
剤、造核剤、銅害防止剤、難燃剤等の一般的に知られて
いるポリプロピレン用添加剤の1つ又は複数が添加され
ていても良い。さらに炭酸カルシューム、タルク、硫酸
バリウム、ワラストナイト、ガラス繊維等の一般的によ
く知られているポリプロピレン樹脂用無機充填剤の1つ
又は複数が充填されていてもよい。又、カーボン等の一
般によく知られたポリプロピレン用顔料が添加されてい
てもよい。
One or more commonly known additives for polypropylene such as an antioxidant, an ultraviolet ray inhibitor, a nucleating agent, a copper damage inhibitor, a flame retardant and the like may be added to the polypropylene resin. Further, one or more of generally known inorganic fillers for polypropylene resin such as calcium carbonate, talc, barium sulfate, wollastonite, and glass fiber may be filled. Also, generally well-known pigments for polypropylene such as carbon may be added.

本発明に使用される表皮材としては、ナイロン布を裏
打ちした塩化ビニルレザー、塩化ビニル系レザーにポリ
プロピレン又はウレタンの発泡シートを貼り合わせたも
の、ナイロン又はポリエステルの素材を用いた編物系
(例えばトリコット)、織物系(例えばモケット)、不
織布系及び編物、織物、不織布にポリプロピレン、ウレ
タンなどの発泡シートを貼り合わせたものなどを挙げる
ことができる。
Examples of the skin material used in the present invention include vinyl chloride leather lined with nylon cloth, a material obtained by laminating a foamed sheet of polypropylene or urethane to a vinyl chloride-based leather, or a knitted material using a nylon or polyester material (for example, tricot). ), A woven fabric (for example, moquette), a nonwoven fabric, a knitted fabric, a woven fabric, a nonwoven fabric and a foamed sheet made of polypropylene, urethane, or the like.

本発明の貼合成形方法としては、表皮材を成形用の金
型に設置し、金型を閉じた後加熱溶融した熱可塑性樹脂
を金型のゲートより金型内に射出して前記表皮材と積層
させ貼合成形する方法や、上下金型間に表皮材を配設し
上・下金型が未閉鎖の状態で熱可塑性樹脂溶融体を供給
し、上・下金型を合して表皮材と熱可塑性樹脂を貼合一
体化する方法が挙げられる。
As the pasting synthetic method of the present invention, the skin material is placed in a mold for molding, and after closing the mold, the thermoplastic resin heated and melted is injected into the mold from the gate of the mold to form the skin material. Or by laminating and laminating, or by placing a skin material between the upper and lower molds, supplying the thermoplastic resin melt with the upper and lower molds not closed, and combining the upper and lower molds. A method of bonding and integrating the skin material and the thermoplastic resin is exemplified.

〔発明の効果〕〔The invention's effect〕

上述の如く、本発明によるポリプロピレン材料及び成
形方法を用いるときわめて風合保持性の良好な貼合成形
品が得られ、従来手作業でおこなわれている高級品の分
野の自動車内装材等へ高品質、低コストの製品を提供す
ることが可能となった。
As described above, when the polypropylene material and the molding method according to the present invention are used, it is possible to obtain a laminated synthetic product having an extremely good hand holding property. It has become possible to provide quality, low-cost products.

(実施例) 以下に本願発明の実施例を示すが、本願発明はこれら
の実施例により必ずしも限定されるものではない。な
お、貼合成形品の評価は以下の方法で行なった。
(Examples) Examples of the present invention will be described below, but the present invention is not necessarily limited to these examples. In addition, evaluation of the laminated synthetic product was performed by the following method.

風合保持レベル評価法 成形品における表皮材のシボ流れ.毛だおれおよび発
泡体のつぶれを目視または触指により10段階で評価し
た。10のレベルが成形前の表皮材の風合を完全に保持し
たものであり、1のレベルがもとの風合を完全に失った
ものである。自動車内装材としての使用に耐えるのは8
以上のレベルのものである。
Hand holding level evaluation method Grain flow of skin material in molded products. Hair follicles and foam collapse were evaluated visually or by touch with a 10-point scale. A level of 10 completely retains the texture of the skin material before molding, and a level of 1 completely loses the original texture. 8 that can withstand use as an automotive interior material
It is of the above level.

衝撃試験評価法 図1に示すごとく、成形品から切り出した50mm×50mm
のテストピース(4)上に撃芯(2)を置き、荷重
(1)を上方から撃芯(2)上に落下させ、テストピー
ス(4)が破壊される時の荷重(1)の最低の高さをも
って破壊高さとし、破壊エネルギーを下式より算出し
た。
Impact test evaluation method As shown in Fig. 1, 50mm x 50mm cut out from molded product
Place the gun barrel (2) on the test piece (4), drop the load (1) from above onto the gun barrel (2), and set the minimum load (1) when the test piece (4) is broken. The fracture height was defined as the height of the fracture, and the fracture energy was calculated from the following equation.

破壊エネルギー(kg−cm)=荷重(kg)×破壊高さ(c
m) 実施例1〜2 一般射出成形用ポリプロピレン樹脂(住友ノーブレン
AZ564、住友化学工業(株)製MFI=30、エチレンプロピ
レン共重体)100重量部に、下式(I)の有機過酸化物
0.1重量部とを混合し射出成形機のホッパーに供給し、
シリンダー内で分解をおこない、MFIが400g/10分のポリ
プロピレン樹脂を得た。このポリプロピレン樹脂を芯材
樹脂とし、東レ(株)製ポリプロピレン発泡体PPAM1503
0(発泡倍率15倍)を塩化ビニル樹脂製のレザーと貼り
合わせた共和レザー(株)製表皮材との同時賦形.貼合
成形をおこなった。
Breaking energy (kg-cm) = Load (kg) x Breaking height (c
m) Examples 1-2: Polypropylene resin for general injection molding (Sumitomo Noblen)
AZ564, Sumitomo Chemical Co., Ltd. MFI = 30, ethylene propylene copolymer) 100 parts by weight of an organic peroxide of the following formula (I)
0.1 parts by weight and supply to the hopper of the injection molding machine,
Decomposition was performed in a cylinder to obtain a polypropylene resin having an MFI of 400 g / 10 minutes. Using this polypropylene resin as the core material resin, polypropylene foam PPAM1503 manufactured by Toray Industries, Inc.
Simultaneous shaping with Kyowa Leather Co., Ltd. skin material with 0 (expansion ratio 15 times) bonded to leather made of vinyl chloride resin. Paste composite form was performed.

成形用金型としては200mm×200mm×50mm高さのボック
ス金型を用い外表面に表皮材の貼合をおこなった。又成
形機は横型射出ユニットをもつ堅型の100Tプレスで、溶
融樹脂は金型内のゲートを通り、型内に噴射される方式
の金型を使用した。
A box mold having a height of 200 mm x 200 mm x 50 mm was used as a molding die, and a skin material was bonded to the outer surface. The molding machine was a rigid 100T press having a horizontal injection unit, and a molten resin was injected into the mold through a gate in the mold.

均等な樹脂の肉厚で金型の形状を忠実に再現できる最
低成形圧力で成形をおこなったときの表皮材の風合の保
持状態の評価、結果、および成形品の衝撃試験結果を表
Iに示した。
Table I shows the evaluation, results, and the impact test results of the molded product's texture when molded at the minimum molding pressure that can faithfully reproduce the shape of the mold with an even resin thickness. Indicated.

比較例1〜2 一般射出成形用ポリプロピレン樹脂(住友ノーブレン
AZ564、住友化学工業(株)製、MFI=30、エチレン.プ
ロピレン共重合体)を芯材樹脂とし、東レ(株)製ポリ
プロピレン発泡体PPAM15030(発泡倍率15倍)を塩化ビ
ニル樹脂製レザーと貼り合わせた共和レザー(株)との
同時賦形貼合成形を実施例1に示す成形機、金型を用い
表1に示す条件でおこなったが風合いは著しく低下し
た。
Comparative Examples 1-2 Polypropylene resin for general injection molding (Sumitomo Noblen
AZ564, manufactured by Sumitomo Chemical Co., Ltd., MFI = 30, ethylene. (Propylene copolymer) as the core material resin, and simultaneous molding and laminating with Kyowa Leather Co., Ltd., in which Toray Co., Ltd. polypropylene foam PPAM15030 (expansion ratio: 15 times) is bonded to vinyl chloride resin leather. Using the molding machine and the mold shown in Example 1 under the conditions shown in Table 1, the texture was significantly reduced.

実施例3 一般射出成形用ポリプロピレン樹脂(住友ノーブレン
AZ564、住友化学工業(株)製MFI=30、エチレン.プロ
ピレン共重合体)に実施例1と同一の有機過酸化物を0.
2重量部混合し分解したものを芯材樹脂とし、実施例1
に示すと同じ表皮材、成形材、金型を用い成形できる最
低圧力で同時賦形、貼合成形をおこなった。評価結果を
表1に示す。風合はいずれも成形前の表皮材に近いレベ
ルを保持した成形品を得た。
Example 3 Polypropylene resin for general injection molding (Sumitomo Noblen)
AZ564, Sumitomo Chemical Co., Ltd. MFI = 30, ethylene. The same organic peroxide as in Example 1 was added to propylene copolymer).
Example 1 was prepared by mixing and decomposing 2 parts by weight of a core resin.
The same shaping and laminating were performed at the minimum pressure that could be molded using the same skin material, molding material and mold as shown in (1). Table 1 shows the evaluation results. In each case, a molded product having a feeling close to that of the skin material before molding was obtained.

比較例3 有機過酸化物の使用量を0.04重量部とする以外は実施
例3と同様にして貼合成形を行なった。結果を表1に示
す。
Comparative Example 3 A laminated composite was prepared in the same manner as in Example 3 except that the amount of the organic peroxide used was changed to 0.04 parts by weight. Table 1 shows the results.

比較例4 実施例1と同じポリプロピレン樹脂原料に有機過酸化
物を0.5部混合し得られたMFI1800の材料を用い、実施例
1と同じ表皮材設備金型を用い表1に示す条件下で貼合
成形を実施し、風合保持及び衝撃強度の評価をおこなっ
た。風合保持はきわめて良好なレベルにあるが、衝撃強
度が実用に耐えないほど著しく低下した。
Comparative Example 4 A material of MFI1800 obtained by mixing 0.5 parts of an organic peroxide with the same polypropylene resin raw material as in Example 1 was used, and was pasted under the conditions shown in Table 1 using the same skin material equipment mold as in Example 1. The composite molding was performed, and the hand holding and the impact strength were evaluated. The feeling retention was at a very good level, but the impact strength was so low that it could not withstand practical use.

実施例4 実施例1と同一の芯材樹脂を用い、ポリエステル系の
トリコットに軟質ウレタン発泡体(発泡倍率20倍)を貼
り合わせた共和レザー(株)製の表皮材で表1に示す条
件下で同時賦形貼合成形を実施した。風合保持は著しく
良好であった。
Example 4 Using the same core material resin as in Example 1, a skin material made by Kyowa Leather Co., Ltd. was obtained by laminating a soft urethane foam (expansion ratio: 20 times) to a polyester-based tricot under the conditions shown in Table 1. And the simultaneous shaping and laminating was performed. Hand holding was remarkably good.

比較例5〜6 比較例1と同等のポリプロピレン樹脂を芯材とし、実
施例5と同等の表皮材を用い表1に示す条件下で同時賦
形貼合成形を実施し風合保持の評価をおこなった。風合
は著しく低下した。
Comparative Examples 5 to 6 Using the same polypropylene resin as in Comparative Example 1 as the core material, and using the same skin material as in Example 5 under the conditions shown in Table 1, a simultaneous shaping and laminating was performed to evaluate the feeling retention. I did it. The feeling was significantly reduced.

【図面の簡単な説明】[Brief description of the drawings]

図1は、本発明における衝撃試験装置の縦の断面図であ
る。 (1)……荷重 (2)……撃芯 (3)……撃芯先端R 1/2インチ (4)……テストピース (5)……テストピース支持具
FIG. 1 is a vertical sectional view of an impact test apparatus according to the present invention. (1) Load (2) Shooting tip (3) Tip R 1/2 inch (4) Test piece (5) Test piece support

───────────────────────────────────────────────────── フロントページの続き (72)発明者 松本 正人 大阪府高槻市塚原2丁目10番1号 住友 化学工業株式会社内 (72)発明者 臼井 信裕 大阪府高槻市塚原2丁目10番1号 住友 化学工業株式会社内 (72)発明者 松原 重義 大阪府高槻市塚原2丁目10番1号 住友 化学工業株式会社内 (56)参考文献 特開 昭62−134231(JP,A) 特開 昭60−212313(JP,A) 特開 昭62−267344(JP,A) 特開 昭62−263241(JP,A) 特開 昭61−155437(JP,A) ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Masato Matsumoto 2-10-1, Tsukahara, Takatsuki-shi, Osaka Sumitomo Chemical Industries Co., Ltd. (72) Inventor Nobuhiro Usui 2-1-1 Tsukahara, Takatsuki-shi, Osaka Sumitomo Inside Chemical Industry Co., Ltd. (72) Inventor Shigeyoshi Matsubara 2-10-1, Tsukahara, Takatsuki-shi, Osaka Sumitomo Chemical Industry Co., Ltd. (56) References JP-A-62-134231 (JP, A) JP-A-60- 212313 (JP, A) JP-A-62-267344 (JP, A) JP-A-62-263241 (JP, A) JP-A-61-155437 (JP, A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】表皮材と芯材樹脂とからなる貼合成形品の
製造において、芯材樹脂としてメルトフローインデック
スが120〜800g/10分であるポリプロピレン樹脂を用いる
ことを特徴とする同時賦形貼合成形方法。
1. A method for producing a laminated synthetic product comprising a skin material and a core material resin, wherein a polypropylene resin having a melt flow index of 120 to 800 g / 10 minutes is used as the core material resin. Pasting composite method.
JP63233333A 1988-09-16 1988-09-16 Polypropylene resin for pasting synthetic type and pasting synthetic type method Expired - Lifetime JP2899675B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63233333A JP2899675B2 (en) 1988-09-16 1988-09-16 Polypropylene resin for pasting synthetic type and pasting synthetic type method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63233333A JP2899675B2 (en) 1988-09-16 1988-09-16 Polypropylene resin for pasting synthetic type and pasting synthetic type method

Publications (2)

Publication Number Publication Date
JPH0280218A JPH0280218A (en) 1990-03-20
JP2899675B2 true JP2899675B2 (en) 1999-06-02

Family

ID=16953504

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Country Link
JP (1) JP2899675B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3575812B2 (en) * 1992-07-31 2004-10-13 住友化学工業株式会社 Multilayer molded product and method for producing the same
WO1996023029A1 (en) * 1995-01-23 1996-08-01 Showa Denko K.K. Propylene resin composition and molded article thereof
JP2001182215A (en) * 1999-10-15 2001-07-03 Bridgestone Corp Ceiling panel for unit room
JP2001193218A (en) * 1999-10-15 2001-07-17 Bridgestone Corp Storage panel for unit room

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60212313A (en) * 1984-04-06 1985-10-24 Toyota Motor Corp Laminated molding provided with intermediate material
JPS61155437A (en) * 1984-12-27 1986-07-15 Asahi Chem Ind Co Ltd Polyolefin resin composition
JPS62134231A (en) * 1985-12-09 1987-06-17 Showa Denko Kk Preparation of laminate and device therefor
JPH0678454B2 (en) * 1986-05-14 1994-10-05 住友化学工業株式会社 Method for producing filler-containing polypropylene resin composition
JPH0730217B2 (en) * 1986-05-08 1995-04-05 住友化学工業株式会社 Thermoplastic elastomer composition

Also Published As

Publication number Publication date
JPH0280218A (en) 1990-03-20

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