JPS5819347A - Glass fiber-reinforced polypropylene resin composition - Google Patents

Glass fiber-reinforced polypropylene resin composition

Info

Publication number
JPS5819347A
JPS5819347A JP11900781A JP11900781A JPS5819347A JP S5819347 A JPS5819347 A JP S5819347A JP 11900781 A JP11900781 A JP 11900781A JP 11900781 A JP11900781 A JP 11900781A JP S5819347 A JPS5819347 A JP S5819347A
Authority
JP
Japan
Prior art keywords
glass fiber
ethylene
polypropylene
crystalline
weight
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
JP11900781A
Other languages
Japanese (ja)
Other versions
JPS6367499B2 (en
Inventor
Yoshikazu Fujii
義和 藤井
Tatsuyuki Mino
三野 達行
Kaoru Kitadono
馨 北殿
Yuji Ikezawa
勇司 池沢
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
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP11900781A priority Critical patent/JPS5819347A/en
Publication of JPS5819347A publication Critical patent/JPS5819347A/en
Publication of JPS6367499B2 publication Critical patent/JPS6367499B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain FRPP having a excellent high-temperature rigidity and impact strength of a weld, by specifying the viscosity of crystalline PP and using a specified rubbery polymer in a composition comprising crystalline PP, a modified PP and glass fiber. CONSTITUTION:FRPP is composed of crystalline PP(A) having an intrinsic viscosity eta of 1.25-1.45 in tetralin soln. at 135 deg.C, an oxygen-contg. unsaturated, org. compc.-modified PP(B), a silane compd.-treated glass fiber (C) and an ethylene/alpha-olfefin rubbery polymer (D) having an ethylene content of 60-79% and an intrinsic viscosity eta of 1.0-1.7 in xylene soln. at 70 deg.C. If component D is absent, no sufficient high-temperature rigidity can be obtd. If component A is absent, no sufficient impact strength of a weld can be obtd. Thus, the characteristics of FRPP can be obtd. only when components A and B are present in combination.

Description

【発明の詳細な説明】 本発明は機械的強度とくに高温での剛性度およびウェル
ド部(ウェルド部とは溶融した樹脂分 が二方向以上より流れてきて溶着する部嶋をいう。)の
衝撃強度に優れたガラス繊維強化ぼりプロピレン樹脂組
成物に関する。ガラス繊維強化ぼりプロピレン樹脂はそ
の優れた機械的強度および耐熱性ゆえに自動車部品およ
び電気部品等への応用展開が極めて活発にはかれている
DETAILED DESCRIPTION OF THE INVENTION The present invention focuses on mechanical strength, particularly rigidity at high temperatures, and impact strength of weld parts (weld parts are areas where molten resin flows from two or more directions and welds together). This invention relates to a glass fiber-reinforced propylene resin composition that has excellent properties. Due to its excellent mechanical strength and heat resistance, glass fiber-reinforced propylene resin is being actively applied to automobile parts, electrical parts, and the like.

しかしながらガラス繊維強化ポリプロピレン樹脂C以下
略してFRFPと称す)は概して衝撃強度とくにウェル
ド部での強度が著しく低下するために自動車部品の中で
も内装部のインストルメントパネルやエンジンルーム内
の機mtam部品には優れた耐熱性は有しながらも適用
を阻害されるケースが多い。FRPPにおいてウェルド
部の衝撃強度を改良する手法として(1)組成物自体の
衝撃強度を高める。(2)ガラス繊維のアスペクト比(
アスペクト比=纏維の長さ/繊細の直径)の適性化をは
かるおよび(8)41成物の流動性を向上させる。など
があげられる。
However, glass fiber reinforced polypropylene resin (hereinafter abbreviated as FRFP) generally has a significantly lower impact strength, especially at the weld part, so it is not suitable for automotive parts such as instrument panels in the interior and mechanical parts in the engine compartment. Although it has excellent heat resistance, its application is often hindered. As a method for improving the impact strength of the weld part in FRPP, (1) the impact strength of the composition itself is increased. (2) Aspect ratio of glass fiber (
(8) To improve the fluidity of the 41 product. etc.

まず組成物の衝撃強度を高めるにはポリプロピレンとし
てエチレン−プロピレン共重合体を用いることが考えら
れるが反面剛性度の低下が大@<、FRPPとしての特
徴が失なわれる。次に例えばガラス繊維のアスペクト比
を低減するとウェルド強度は若干改良されるもの−、ガ
ラス繊輪を添加させること!得られる高温での剛性度が
損われる。さらに組成物の流動性を向上させることでウ
ェルド部を形成する時の溶融樹脂の接合スピードを高め
、ウェルド強度を若干改良させることが定性的に言われ
ているが実質的な効果としては小さい。仁のように高温
での剛性度とウェルド部の衝撃強度を両立させることは
非常に難しいのが現吠であった。本発明者らはガラス繊
細強化ぼりプロピレン樹脂組成物のうち主要成分である
結晶性ポリプロピレン。
First, in order to increase the impact strength of the composition, it is possible to use an ethylene-propylene copolymer as the polypropylene, but on the other hand, the rigidity is greatly reduced, and the characteristics of FRPP are lost. Next, for example, if the aspect ratio of glass fibers is reduced, the weld strength will be slightly improved - by adding glass fiber rings! The resulting high temperature stiffness is impaired. Furthermore, it is qualitatively said that improving the fluidity of the composition increases the joining speed of the molten resin when forming the weld part and slightly improves the weld strength, but the actual effect is small. It was very difficult to achieve both high-temperature rigidity and impact strength of the welded part like Jin, which is the case with Genbo. The present inventors have developed a crystalline polypropylene which is the main component of a glass delicate reinforced propylene resin composition.

変性したポリプロピレン、ガラス繊維についてそれらの
種類、量を変えさらにそれらの組合せについても検討し
たが顕著な効果は認められなかった。
Although different kinds and amounts of modified polypropylene and glass fibers were used, and combinations thereof were also investigated, no significant effects were observed.

前記の通り、ゴム状重合体をさらに添加すると高温での
剛性度が低下することは廖実であるが、ゴム状重合体の
sgi*やそれらの量昏こつ0て種々検討した結果とく
に結晶性ぼりプロピレンとの組合せを留意することで優
れた高温での剛性度およびウェルド部の衝撃強度を有す
るFRFPが得られることを見出した。さらに詳しく述
べれば[11(185℃、テトラリン溶液の極限粘度)
が1.26〜1.46好ましくは′1・oo〜1・40
でエチレン含有量が4優以下の結晶性プリプロピレンと
[11(70℃、キシレン溶液の極限粘度)がLO〜1
.7好ましくは1.8〜1.6でエチレン含有量が60
〜79q6のゴム状重合体とを組合せ、所定量の含酸素
不飽和有機化合物で変性したポリプロピレンおよびシラ
ン化合物で表面処理を細したガラス繊細とを加えてなる
樹脂組成物が優れた高温での剛性度、およびウェルド部
の衝撃強度を発揮する。その理由は必ずしも明らかでな
いが〔−〕が1.26〜1.45でエチレン含有量が4
優以下の結晶性ポリプロピレンを用いてもゴム状重合体
の〔1〕が1.0〜1.7でかつエチレン含有量が60
〜79粥の範囲カラ外れるものであれば十分な高温での
剛性度が得られず、又逆に〔−〕が1.0〜1.7でか
つエチレン含有量が60〜79%のゴム状重合体を用い
ても結晶性ポリプロピレンが前述の構造から外れるもの
であれば十分なウェルド部強度が得られないことを総じ
て考えると両成分が同時に存在する場合にのみ発現され
る特徴であると思われる。すなわち[11が1.26〜
1.46好ましくは1.30〜1.40である結晶性ポ
リプロピレン内と含酸素不飽和有機化合物で変性したポ
リプロピレン■とシラン系化合物で表面処理を施したガ
ラス繊維0および〔−〕が1. O−1,7でエチレン
含有量が60〜79%のゴム状重合体υとからなるガラ
ス繊維強化ポリプロピレン樹脂組成物は機械的強度とく
に高温での剛性度およびウェルド部の衝撃強度に優れる
ものであり、とくに自動車部品の中でも内装の機能部品
用材料としてまさに好適である。本発明の組成物に使用
される結晶性ポリプロピレンとしてはポリプロピレン、
プロピレンエチレン共重合体などが挙げられ[1〕(1
85℃、テトラリン溶液の極限粘度)が1.20〜1.
40でエチレン含有量が4%以下のものである0本発明
の組成物に使用される含酸素不飽和有機化合物で変性し
たがりプロピレンとしては特に限定されず公知のものが
使用できるが一般にはポリプロピレン単独重合体、エチ
レンプロピレン共重合体などのポリプロピレンとアクリ
ル酸、メタアクリル酸、マレイン酸、イタコン酸、フマ
ル酸、無水マレイン酸、無水イタコン酸等の酸又は酸無
水物ユニットを有する含酸素不飽和有機化合物との共重
合体又はグラフト共重合体等が使用される。と(1m/
mプリピレンとアクリル酸又は無水マレイン酸の共重合
体又はグラフト共重合体が好ましい6次に本発明の組成
物に使用されるガラス繊維は通常のガラス繊細強化樹脂
に使用されるもので一般的には6〜20Fの直径のもの
でありシラン系化合物で表面処理が施されるが、その表
面処理剤としてはβ−(8,4−エポキシシクロヘキシ
ル)−二チルトリメトキシシラン。
As mentioned above, it is true that the stiffness at high temperatures decreases when a rubbery polymer is further added, but as a result of various studies on the SGI* of the rubbery polymer and their amount It has been found that by paying attention to the combination with propylene, it is possible to obtain a FRFP with excellent rigidity at high temperatures and impact strength of the weld portion. In more detail, [11 (185°C, intrinsic viscosity of tetralin solution)
is 1.26 to 1.46, preferably '1·oo to 1·40
Crystalline propylene with an ethylene content of 4 or less and [11 (70°C, intrinsic viscosity of xylene solution) is LO ~ 1]
.. 7 Preferably 1.8 to 1.6 with an ethylene content of 60
A resin composition made by combining a rubber-like polymer of ~79q6 with polypropylene modified with a predetermined amount of an oxygen-containing unsaturated organic compound and glass finely treated with a silane compound has excellent rigidity at high temperatures. degree, and the impact strength of the weld area. The reason is not necessarily clear, but [-] is 1.26 to 1.45 and the ethylene content is 4.
Even if crystalline polypropylene with a crystallinity below excellent is used, the [1] of the rubbery polymer is 1.0 to 1.7 and the ethylene content is 60.
If it is outside the range of ~79 porridge, sufficient rigidity at high temperatures will not be obtained, and conversely, if [-] is 1.0 to 1.7 and the ethylene content is 60 to 79%, it will be rubbery. Considering that even if a polymer is used, sufficient weld strength cannot be obtained if the crystalline polypropylene deviates from the above-mentioned structure, it seems that this characteristic is only expressed when both components are present at the same time. It will be done. That is, [11 is 1.26~
1.46 Preferably 1.30 to 1.40 in crystalline polypropylene, polypropylene (2) modified with an oxygen-containing unsaturated organic compound, and glass fibers 0 and [-] surface-treated with a silane compound. A glass fiber-reinforced polypropylene resin composition consisting of a rubber-like polymer υ with O-1,7 and an ethylene content of 60 to 79% has excellent mechanical strength, particularly rigidity at high temperatures and impact strength of the weld part. It is especially suitable as a material for functional interior parts among automobile parts. The crystalline polypropylene used in the composition of the present invention includes polypropylene,
Examples include propylene ethylene copolymer [1] (1
85°C, the intrinsic viscosity of the tetralin solution is 1.20 to 1.
40 and has an ethylene content of 4% or less.Propylene is modified with the oxygen-containing unsaturated organic compound used in the composition of the present invention.Propylene is not particularly limited and any known propylene can be used, but in general polypropylene Homopolymers, polypropylenes such as ethylene-propylene copolymers, and oxygen-containing unsaturated compounds containing acid or acid anhydride units such as acrylic acid, methacrylic acid, maleic acid, itaconic acid, fumaric acid, maleic anhydride, itaconic anhydride, etc. Copolymers or graft copolymers with organic compounds are used. and (1m/
A copolymer or graft copolymer of m-propylene and acrylic acid or maleic anhydride is preferred.6 Next, the glass fibers used in the composition of the present invention are those used in ordinary glass fine reinforced resins and are generally has a diameter of 6 to 20F and is surface treated with a silane compound, and the surface treatment agent used is β-(8,4-epoxycyclohexyl)-dityltrimethoxysilane.

γ−グリシドキシプロビルトリメトキシシランなどのエ
ポキシシラン、ビニルトリエトキシシラン、ビニルトリ
クロロシランなどのビニルシラン、r−アミノプロピル
トリエトキシシラン。
Epoxysilanes such as γ-glycidoxypropyltrimethoxysilane, vinylsilanes such as vinyltriethoxysilane and vinyltrichlorosilane, and r-aminopropyltriethoxysilane.

N−β−(アミノエチル)−r−アミノプロピルトリメ
トキシシランなどのアミノシランから選ばれた少なくと
も1種の処理剤を用いる0表面処理を施す方法としては
通常シラン系化合物による表面処理剤の溶液に浸漬した
後乾燥する方法が用いられる。最後に本発明の組成物に
使用されるゴム伏重合体としてはエチレン−ブロンモノ
マー共重合体およびエチレン−ブテン共重合体などが挙
げられ、〔η〕が1.0〜1,7でエチレン含有量が6
0〜79粥のものである0本発明では前述した結晶性ポ
リプロピレン、変性したポリプロピレン、ガラス繊維お
よびゴム状重合体を混合する場合に各成分をできるだけ
均一ニ分散することが必要でこの目的のためにはバンバ
リーミキサ−、スクリュー押出機、ロールミルなどを使
用することができる。又本発明の組成物に一般的な各種
の酸化防止剤、紫外線吸収剤等の安定剤および一般的な
顔料、無機充填剤等の添加は任意になし得る6次に本発
明を実施例および比咬例によりさらに具体的に説明する
A method for performing surface treatment using at least one treatment agent selected from aminosilanes such as N-β-(aminoethyl)-r-aminopropyltrimethoxysilane is usually performed using a solution of a surface treatment agent using a silane compound. A method of soaking and then drying is used. Finally, rubber polymers used in the composition of the present invention include ethylene-brone monomer copolymers and ethylene-butene copolymers, which have an [η] of 1.0 to 1.7 and contain ethylene. amount is 6
0 to 79 gruel 0 In the present invention, when mixing the aforementioned crystalline polypropylene, modified polypropylene, glass fiber, and rubbery polymer, it is necessary to disperse each component as uniformly as possible, and for this purpose. A Banbury mixer, screw extruder, roll mill, etc. can be used for this purpose. In addition, various general antioxidants, stabilizers such as ultraviolet absorbers, general pigments, inorganic fillers, etc. can be optionally added to the composition of the present invention. This will be explained in more detail using bite examples.

*施例1 結晶性ポリプロピレンA(Cη) = 1.8、エチレ
ン含有量1q6)、B ([’2”l =−1,a 5
、エチレン含有量8.5%)又は0 ((tl = 1
. s。
*Example 1 Crystalline polypropylene A (Cη) = 1.8, ethylene content 1q6), B (['2"l = -1, a5
, ethylene content 8.5%) or 0 ((tl = 1
.. s.

エチレン含有量O優)と変性したポリプロピレン(日本
ライヒホールド社製がリボシド1001 )とガラス繊
維(日本硝子繊維製RE806−TP87)およびゴム
状重合体A(C’l〕−1,4、エチレン含有量70%
のエチレンプロプレン共重合体)、B〔[η]=1.8
゜エチレン含有1i78q6のエチレンブテン共重合体
)又はC(r’?) = 1. Lエチレン含有量65
%のエチレンプロピレン共重合体)の各々の所定量と酸
化防止剤も含め粉体混合機で2分湯合し1.温度220
℃でべ氷ト付スクリュー押出機(スクリュー66−0.
 (1,R,=8.01を使用し押出ペレットを作成し
た。得られた組成物を樹脂湿度280℃、圧力s’ro
b/cd。
Ethylene content O), modified polypropylene (Riboside 1001 manufactured by Nippon Reichhold Co., Ltd.), glass fiber (RE806-TP87 manufactured by Nippon Glass Fibers) and rubbery polymer A (C'l]-1,4, containing ethylene. Amount 70%
ethylene proprene copolymer), B [[η] = 1.8
゜Ethylene-containing 1i78q6 ethylene-butene copolymer) or C(r'?) = 1. L ethylene content 65
% ethylene propylene copolymer) and an antioxidant for 2 minutes in a powder mixer.1. temperature 220
A screw extruder (screw 66-0.
(1, R, = 8.01 was used to create extruded pellets.The resulting composition was heated at a resin humidity of 280°C and a pressure of
b/cd.

トータルサイクル40秒の射出成形条件にて所定の試験
片に作成し、物性試験を行なった。
A predetermined test piece was prepared under injection molding conditions with a total cycle of 40 seconds, and a physical property test was conducted.

但しウェルド部のアイゾツト衝撃試験片は試験片両端に
ゲートを設は中央部にウェルド部を形成させ、アイゾヴ
ト衝撃試験ではこのウェルド部をハンマーかた−くよう
調整し実施した。
However, the IZOVT impact test piece had gates at both ends of the test piece and a weld part was formed in the center, and the IZOVT impact test was conducted by adjusting the weld part to make it harder with a hammer.

得られた結果をまとめて第1表に示す、結晶性ポリプロ
ピレンA又はBとゴム吠重合体人又はBが該組成物中に
同時に存在する実施例中のサンプル1.2および8が高
温での剛性度とウェルド部強度で優れた特性を有してい
ることが比較例(サンプル4.5)と対比しても明らか
である。
The results obtained are summarized in Table 1. Samples 1.2 and 8 in the examples in which crystalline polypropylene A or B and rubber polymer or B are simultaneously present in the composition are shown in Table 1. It is clear from comparison with the comparative example (sample 4.5) that it has excellent properties in terms of rigidity and weld strength.

Claims (1)

【特許請求の範囲】 (1)  (11(185℃、テトラリン溶液の極限粘
度)が1.26〜1.46である結晶性ポリプロピレン
因と含酸素不飽和有機化合物で変性したポリプロピレン
の)とシラン系化合物で表面処理を施したガラス繊維(
L)および〔η〕(70℃、キシレン溶液の極限粘度)
が1.o〜!、7でエチレン含有量が60〜79q6の
エチレン−5−オレフィン系ゴム状重合体0とからなる
ガラス繊維強化ポリプロピレン樹脂組成物。 (2)  [7]が1.80〜1.40 テ二f L/
 ン含有量が4優以下の結晶性ポリプロピレンおよヒ[
t〕が1.8〜1.6でエチレン含有量が68〜76倦
のゴムぜ重合体を用いてなる特許請求の範囲第1項記載
のガラス繊維強化ポリプロピレン樹脂組成物。 (8)結晶性ポリプロピレン(2)80〜70重11%
と含酸素不飽和有機化合物で変性したポリプロピレン@
10〜20重量倦とシラン化合物で表面処理を施したガ
ラス繊維(0)15〜86重量%およびゴム状重合体0
5〜1,6重量倦とからなる特許請求の範囲、第1項記
載のガラス繊維強化ポリプロピレン樹脂組成物。
[Scope of Claims] (1) (Crystalline polypropylene whose 11 (intrinsic viscosity of tetralin solution at 185°C) is 1.26 to 1.46 and polypropylene modified with an oxygen-containing unsaturated organic compound) and silane Glass fibers surface-treated with chemical compounds (
L) and [η] (70°C, intrinsic viscosity of xylene solution)
is 1. o~! , 7 and 0 of an ethylene-5-olefin rubber-like polymer having an ethylene content of 60 to 79q6. (2) [7] is 1.80 to 1.40 Ten2f L/
Crystalline polypropylene with a content of 4 or less
t] of 1.8 to 1.6 and an ethylene content of 68 to 76. (8) Crystalline polypropylene (2) 80-70% by weight 11%
and polypropylene modified with oxygen-containing unsaturated organic compounds@
10-20% by weight, 15-86% by weight of glass fiber (0) surface-treated with a silane compound, and 0% by weight of rubbery polymer.
The glass fiber reinforced polypropylene resin composition according to claim 1, comprising a weight of 5 to 1.6.
JP11900781A 1981-07-28 1981-07-28 Glass fiber-reinforced polypropylene resin composition Granted JPS5819347A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11900781A JPS5819347A (en) 1981-07-28 1981-07-28 Glass fiber-reinforced polypropylene resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11900781A JPS5819347A (en) 1981-07-28 1981-07-28 Glass fiber-reinforced polypropylene resin composition

Publications (2)

Publication Number Publication Date
JPS5819347A true JPS5819347A (en) 1983-02-04
JPS6367499B2 JPS6367499B2 (en) 1988-12-26

Family

ID=14750681

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11900781A Granted JPS5819347A (en) 1981-07-28 1981-07-28 Glass fiber-reinforced polypropylene resin composition

Country Status (1)

Country Link
JP (1) JPS5819347A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5896640A (en) * 1981-12-04 1983-06-08 Idemitsu Petrochem Co Ltd Polypropylene-based resin composition and its manufacture
JPS59226041A (en) * 1983-06-08 1984-12-19 Mitsubishi Petrochem Co Ltd Filler-containing propylene polymer composition
JPS6069146A (en) * 1983-09-26 1985-04-19 Mitsubishi Petrochem Co Ltd Glass fiber-reinforced pigmented propylene resin composition
JPS60163950A (en) * 1984-02-07 1985-08-26 Asahi Chem Ind Co Ltd Polypropylene resin composition
US4603153A (en) * 1983-06-08 1986-07-29 Mitsubishi Petrochemical Co., Ltd. Glass fiber reinforced resin composition
JPS61236844A (en) * 1985-04-12 1986-10-22 Ube Ind Ltd Reinforced polypropylene composition
US5369173A (en) * 1989-06-13 1994-11-29 Sumitomo Chemical Company, Limited Glass fiber-reinforced resin composition
US5376701A (en) * 1990-01-15 1994-12-27 Exxon Chemical Patents Inc. Thermoplastic polymer fibre composition
KR20010054822A (en) * 1999-12-08 2001-07-02 유현식 Polypropylene resin composition having thermal resistance, high rigidity and low warpage properties

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS528054A (en) * 1975-07-10 1977-01-21 Mitsui Petrochem Ind Ltd Glass-fiber reinforced polyolefin composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS528054A (en) * 1975-07-10 1977-01-21 Mitsui Petrochem Ind Ltd Glass-fiber reinforced polyolefin composition

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5896640A (en) * 1981-12-04 1983-06-08 Idemitsu Petrochem Co Ltd Polypropylene-based resin composition and its manufacture
JPS6365101B2 (en) * 1981-12-04 1988-12-14
JPS59226041A (en) * 1983-06-08 1984-12-19 Mitsubishi Petrochem Co Ltd Filler-containing propylene polymer composition
US4603153A (en) * 1983-06-08 1986-07-29 Mitsubishi Petrochemical Co., Ltd. Glass fiber reinforced resin composition
JPS6069146A (en) * 1983-09-26 1985-04-19 Mitsubishi Petrochem Co Ltd Glass fiber-reinforced pigmented propylene resin composition
JPS60163950A (en) * 1984-02-07 1985-08-26 Asahi Chem Ind Co Ltd Polypropylene resin composition
JPS61236844A (en) * 1985-04-12 1986-10-22 Ube Ind Ltd Reinforced polypropylene composition
JPH0535738B2 (en) * 1985-04-12 1993-05-27 Ube Industries
US5369173A (en) * 1989-06-13 1994-11-29 Sumitomo Chemical Company, Limited Glass fiber-reinforced resin composition
US5376701A (en) * 1990-01-15 1994-12-27 Exxon Chemical Patents Inc. Thermoplastic polymer fibre composition
KR20010054822A (en) * 1999-12-08 2001-07-02 유현식 Polypropylene resin composition having thermal resistance, high rigidity and low warpage properties

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