JPH03185038A - Polypropylene resin composition - Google Patents

Polypropylene resin composition

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Publication number
JPH03185038A
JPH03185038A JP32516389A JP32516389A JPH03185038A JP H03185038 A JPH03185038 A JP H03185038A JP 32516389 A JP32516389 A JP 32516389A JP 32516389 A JP32516389 A JP 32516389A JP H03185038 A JPH03185038 A JP H03185038A
Authority
JP
Japan
Prior art keywords
weight
mica
polypropylene resin
elastic modulus
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.)
Granted
Application number
JP32516389A
Other languages
Japanese (ja)
Other versions
JP2843391B2 (en
Inventor
Ei Shimizu
清水 映
Katsunori Takamoto
高本 克則
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.)
Kuraray Co Ltd
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Kuraray Co Ltd
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Priority to JP32516389A priority Critical patent/JP2843391B2/en
Publication of JPH03185038A publication Critical patent/JPH03185038A/en
Application granted granted Critical
Publication of JP2843391B2 publication Critical patent/JP2843391B2/en
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Abstract

PURPOSE:To provide the subject composition having high elastic modulus and inner loss and useful for producing lightweight molded products by incorporating in a specific ratio inorganic fillers including mica having a specific weight- average flake diameter and a specified weight-average aspect ratio into the composition. CONSTITUTION:The objective composition comprises a polypropylene resin and <=20wt.% of inorganic fillers including 3-15wt.% of mica (white mica) having a weight-average flake diameter of 10-700mum and a weight-average aspect ratio of >=10. The polypropylenic resin is e.g. a modified resin prepared by activating polypropylene resin and subsequently addition-reacting maleic acid, etc., to the activated polypropylene resin.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、木材、パルプ紙などがその機能的特徴を生か
して用いられている用途において、特に好適にその代替
として用いられるポリプロピレン系樹脂組成物に関する
[Detailed Description of the Invention] [Field of Industrial Application] The present invention provides a polypropylene resin composition that is particularly suitable as a substitute for wood, pulp paper, etc. in applications where they are used to take advantage of their functional characteristics. relating to things.

〔従来の技術〕[Conventional technology]

従来、木材、パルプ紙などが用いられてきた用途におい
て、例えばデザインの自由度が低い、成形組立に要する
時間が長い、乾湿状態において物性変化が大きいなどの
問題点を有する木材、パルプ紙などの問題点を改善する
ため、最近合成木材、合成紙の開発が進められており、
木材、パルプ紙などが持つ機能的特性、例えば高弾性率
、高内部損失を併せもつ素材として結晶性ポリオレフィ
ン樹脂組成物が報告されている(特開昭61−1639
45号公報参照)。
In applications where wood, pulp paper, etc. have traditionally been used, wood, pulp paper, etc. have problems such as low degree of freedom in design, long time required for molding and assembly, and large changes in physical properties in wet and dry conditions. In order to improve this problem, synthetic wood and synthetic paper have recently been developed.
A crystalline polyolefin resin composition has been reported as a material that has the functional properties of wood, pulp paper, etc., such as high elastic modulus and high internal loss (Japanese Patent Application Laid-Open No. 1639-1639).
(See Publication No. 45).

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

しかるに、結晶性ポリオレフィン樹脂組酸物は、樹脂が
結晶性であるために成形前後の体積収縮率が大きく、成
形物にひげが生じる。このひけを改善するためには無機
充填材を多量に用いる必要があり、そのため成形物の密
度が高くなる問題があった。
However, since the resin of the crystalline polyolefin resin combination acid is crystalline, the volumetric shrinkage rate before and after molding is large, and the molded product has whiskers. In order to improve this sink mark, it is necessary to use a large amount of inorganic filler, which poses a problem of increasing the density of the molded product.

而して1本発明の目的は、高弾性率および高内部損失を
有し、かつ軽量化された成形物を得るためのポリプロピ
レン系樹脂組成物を提供することにある。
SUMMARY OF THE INVENTION An object of the present invention is to provide a polypropylene resin composition that has a high modulus of elasticity and a high internal loss, and is capable of producing lightweight molded products.

〔課題を解決するための手段〕[Means to solve the problem]

本発明によれば、上記の目的は、ポリプロピレン系樹脂
および重量平均フレーク径が10〜700μであり、t
it平均アスペクト比が10以上であるマイカ3〜15
重!に%を必須成分とする樹脂組成物であって、マイカ
を含めた光項材の含有率が20@量%以下であることを
特徴とするポリプロピレン系樹脂組成物を提供すること
によって達成される。
According to the present invention, the above object is to use a polypropylene resin and a weight average flake diameter of 10 to 700μ, and t
Mica 3 to 15 with an average aspect ratio of 10 or more
Heavy! This is achieved by providing a polypropylene-based resin composition, which is a resin composition containing % as an essential component, and is characterized in that the content of photonic materials including mica is 20% by mass or less. .

本発明において用いられるポリプロピレン系樹脂につい
ては特に制限はないが、マイカとの親和性を有するよう
に化学変性がなされていることが好筐しい。化学変性が
なされたポリプロピレンとはポリプロピレンと不飽和化
合物の反応により得られる樹脂であり、かかる樹脂は例
えば過酸化物。
There are no particular restrictions on the polypropylene resin used in the present invention, but it is preferably chemically modified to have an affinity for mica. Chemically modified polypropylene is a resin obtained by reacting polypropylene with an unsaturated compound, and such a resin is, for example, a peroxide.

放側線などにより活性化されたポリプロピレン樹脂に、
マレインa、 無水マレイン酸、フマル酸、アクリル酸
、メタクリル酸、グリシジルメタクリレート、グリシジ
ルアクリレート、シランカップリング剤などの化合物を
付加lたはグラフト重合させることにより製造される。
Polypropylene resin activated by radial radiation etc.
It is produced by addition or graft polymerization of compounds such as maleic a, maleic anhydride, fumaric acid, acrylic acid, methacrylic acid, glycidyl methacrylate, glycidyl acrylate, and a silane coupling agent.

これらの化合物についての混合率について特に制限はな
いが、ポリプロピレン樹脂の重量に対して通常0.03
〜3重量蝿である。また、本発明のポリプロピレン系樹
脂はアクリル酸アルキルエステルまたはメタクリル酸ア
ルキルエステルを共重合した脂肪族ポリオレフィン、エ
チレンなどの共重合成分等を含有していても差し支えな
い。さらに本発明のポリプロピレン系樹脂は、化学変性
されたポリプロピレンと未変性のポリプロピレンが混合
されたものであってもよい。
There are no particular restrictions on the mixing ratio of these compounds, but it is usually 0.03% by weight of the polypropylene resin.
~3 weight fly. Further, the polypropylene resin of the present invention may contain an aliphatic polyolefin copolymerized with an alkyl acrylate or an alkyl methacrylate, a copolymer component such as ethylene, and the like. Furthermore, the polypropylene resin of the present invention may be a mixture of chemically modified polypropylene and unmodified polypropylene.

本発明において用いられるマイカは、白マイカ。The mica used in the present invention is white mica.

金マイカ、合成マイカなどから広く選ぶことができ、重
量平均フレーク径が10〜700μの範囲であり、in
平均アスペクト比が10以上である。
You can choose from a wide range of gold mica, synthetic mica, etc., and the weight average flake diameter is in the range of 10 to 700μ.
The average aspect ratio is 10 or more.

重量平均フレーク径がlOμ未満および700μる成形
物の弾性率が極端に低い。重−1XF−均フレーク径が
15〜500μの範囲であり、重量平均アスペクト比が
20以上、特に35以上のマイカを用いるのが好筐しい
The elastic modulus of molded products with weight average flake diameters of less than 10μ and 700μ is extremely low. It is preferable to use mica having a weight average flake diameter of 15 to 500 μm and a weight average aspect ratio of 20 or more, especially 35 or more.

マイカの重量平均アスペクト比とは下記の方法で測定し
7た重量平均フレーク径りと重量平均フレーク厚さdよ
り(1)式を用いて求められる値である。
The weight-average aspect ratio of mica is a value determined using equation (1) from the weight-average flake diameter and weight-average flake thickness d measured by the following method.

重量平均アスペクト比= X / d    (1)こ
こでマイカ粉末の重量平均フレーク径2とVi、マイカ
粉末を各種の目開きの標準ふるいを用いて銖 湿式分会を行い、その結果をRosin−1(Amml
ar 4図にプロットして測定に供したマイカ粉体の5
0重it%が通過するふるいの目開きL6Gを求め、そ
の値から(2)式により算出した値である。
Weight average aspect ratio = Amml
ar 5 of the mica powder plotted in Figure 4 and subjected to measurement
The opening L6G of the sieve through which 0 weight it% passes is determined, and the value is calculated from the obtained value using equation (2).

1’ =l”i nso             (
2)筐たマイカ粉末の1M号平均フレーク厚さdとは。
1' = l”inso (
2) What is the 1M average flake thickness d of the cased mica powder?

C,E、Capesらの報告による水面単粒子脱法(C
,E。
Water surface single particle removal method reported by C, E, Capes et al.
,E.

Capes and R,C,Coleman、 In
d、Eng、Chem、Fundam、、 12゜12
4(1973))により測定されるフレークの水面での
占有面!R8を弔いて、(8)式より算出される値であ
る。
Capes and R.C., Coleman, In.
d, Eng, Chem, Fundam,, 12°12
4 (1973)) occupied by the flake at the water surface! This is a value calculated from equation (8), excluding R8.

ここでWは、測定に供したフレークの重量、Sはフレー
クの水面での占有面積、ρはフレークの比重、(1−ε
)は、フレークが水面上で最密充填状態をとった場合の
占有率であり、フレークが雲母の場合にはρの値として
は2.86f/−が、(1−ε)の値としては0.9が
、計算に際して用いられる。
Here, W is the weight of the flakes subjected to measurement, S is the area occupied by the flakes on the water surface, ρ is the specific gravity of the flakes, (1-ε
) is the occupancy rate when the flakes are in a close-packed state on the water surface, and when the flakes are mica, the value of ρ is 2.86f/-, and the value of (1-ε) is 2.86f/-. 0.9 is used in the calculation.

マイカの配合率は全組成物量の3〜15重量多の範囲で
あり、5〜IO重量多の範囲が好ましい。
The blending ratio of mica is in the range of 3 to 15% by weight of the total composition, preferably in the range of 5 to 10% by weight.

配合率が3重量1%未満の場合、得られる成形物の弾性
率および内部損失が低下する。また配合率が15重量悌
を越える場合、成形物の軽量化という効果が奏されない
If the blending ratio is less than 3% by weight, the elastic modulus and internal loss of the resulting molded product will decrease. Furthermore, if the blending ratio exceeds 15% by weight, the effect of reducing the weight of the molded product cannot be achieved.

本発明において用いられるマイカは、マトリックス樹脂
に対して良好な親和性を有するようにシランカップリン
グ剤等による表面処理がなされていることが好ましい。
The mica used in the present invention is preferably surface-treated with a silane coupling agent or the like so that it has good affinity for the matrix resin.

該シランカップリング剤としては、γ−アミノプロピル
トリメトキシシラン、γ−アミノプロピルトリエトキシ
シラン、N−(β−アミノエチル)−γ−アミノプロピ
ルトリメト乞 キシシラン等φあげることができる。これらシランカツ
プリング削の配合割合に関しては、特に制限はないが、
一般的にはマイカの重量に対して0.05〜3重量多で
ある。なお、シランカッブリング剤尋の表酊処理剤は、
予め、マイカを表面処理する方法で用いてもよいが、樹
脂とマイカを溶融混練する際、直接添加i−でも効果を
発揮する。
Examples of the silane coupling agent include γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, and the like. There are no particular restrictions on the blending ratio of these silane coupling cutters, but
Generally, it is 0.05 to 3 more by weight than the weight of mica. In addition, the surface alcohol treatment agent for silane coupling agent is:
Although mica may be used by surface-treating it in advance, it is also effective to directly add i- when melting and kneading the resin and mica.

本発明においては、マイカの他にガラス繊m。In the present invention, glass fiber m is used in addition to mica.

ウオラストナイト、タルク、ガラスフレーク、炭素偵維
、グラファイト、炭酸カルシウム、硫酸バリウムなどの
無機充填材を添加することができる。
Inorganic fillers such as wollastonite, talc, glass flakes, carbon fibers, graphite, calcium carbonate, barium sulfate, etc. can be added.

特にマイカの配合率が5を遺憾未満の場合%得られろ成
形物の軽量化は奏されるが、弾性率i6よび内部損失が
やや劣るため成形物の弾性率および内部損失を一1eめ
るうえでウオラストナイト、タルク。
In particular, when the blending ratio of mica is less than 5%, the weight of the molded product can be reduced, but the elastic modulus and internal loss of the molded product are slightly inferior, so the modulus of elasticity and internal loss of the molded product must be lowered by 1e. Uedewolastonite, talc.

グラファイトなどをマイカと併用することが好まり、い
。その場合、マイカを含む無機充填材の配合率tま全組
成物隈の20重′gc係以下であり、15重ffi%以
下であることが好″?!Lい。マイカを含む充填材の配
合率が20重重量を越える場合、得られる成形物の密度
が高くなり、成形物の軽量化が損われるとともに成形物
の比弾性率(弾性率/密度)が低下する。
It is preferable to use graphite etc. together with mica. In that case, it is preferable that the blending ratio of the inorganic filler containing mica is less than 20% by weight of the total composition, and preferably less than 15% by weight. If the blending ratio exceeds 20 weight, the density of the resulting molded product becomes high, the weight reduction of the molded product is impaired, and the specific elastic modulus (elastic modulus/density) of the molded product decreases.

本発明の組成物には発泡剤を添加することができ1発泡
剤の種類については特に制限はないが、例えばアゾジカ
ルボンアミド、ジニトロソペンタメチレンテトラミン、
p、p’−オキシビス(ベンゼンスルホニルヒドラジド
)などの窒素化合物や重炭酸ソーダなどの炭酸化合物等
の化学発泡剤、窒素、空気などの物理発泡剤を挙げるこ
とができる。
A blowing agent may be added to the composition of the present invention, and there are no particular restrictions on the type of blowing agent, such as azodicarbonamide, dinitrosopentamethylenetetramine,
Examples include chemical blowing agents such as nitrogen compounds such as p,p'-oxybis(benzenesulfonyl hydrazide) and carbonate compounds such as sodium bicarbonate, and physical blowing agents such as nitrogen and air.

これらの発泡剤は、ステアリン酸カルシウム、2ウリン
酸亜鉛などの発泡助剤と併用してもよい。
These foaming agents may be used in combination with foaming aids such as calcium stearate and zinc diurate.

発泡倍率は1.1〜1.5倍の範囲が好ましい。豊た、
得られる成形物の性能を損わない範囲内で着色剤、可塑
剤、滑剤、酸化防止剤、銅害防止剤など公知の添加剤を
加えることもできる。
The expansion ratio is preferably in the range of 1.1 to 1.5 times. Rich,
Known additives such as colorants, plasticizers, lubricants, antioxidants, and copper damage inhibitors can also be added within a range that does not impair the performance of the resulting molded product.

本発明の組成物は、一般的には各成分を単軸押出機、二
軸押出機、ロール混練機等によシ混練した後、射出成形
機、押出成形機、圧縮成形機、カレンダー成形機等に供
給され各種形状の成形物に成形される。
The composition of the present invention is generally prepared by kneading each component in a single screw extruder, twin screw extruder, roll kneader, etc., and then using an injection molding machine, extrusion molding machine, compression molding machine, or calendar molding machine. etc., and molded into molded products of various shapes.

このようにして得られた成形物は、密度が1.Oy/c
rA以下と小さいうえに弾性率が2.0X10”dyn
/7″以上と大きいことから比弾性率が高く。
The molded product thus obtained has a density of 1. Oy/c
Small, less than rA, and elastic modulus of 2.0X10”dyn
The specific elastic modulus is high due to its large size of /7″ or more.

内部損失も高いのでスピーカーボックス、音響振動板な
どの音響機器等に有用である。
Since it has a high internal loss, it is useful for audio equipment such as speaker boxes and acoustic diaphragms.

〔作用〕[Effect]

本発明によれば、ポリプロピレン系衝折に特定形状のマ
イカを少量添加することにより1弾性率および内部損失
に浚れているだけでなく、4i’Jt化された成形物を
得ることができる。
According to the present invention, by adding a small amount of mica of a specific shape to polypropylene-based crushing, it is possible to obtain a molded product that not only has a modulus of elasticity of 1 and an internal loss but also has a 4i'Jt.

〔実施例〕〔Example〕

以下、実施例を挙げて本発明を説明するが、これらの実
施例は本発明を何ら制限するものではない。なお、実施
例中の弾性率は動的弾性率によって評価し、渣た各物性
は下記の方法により測定した。
EXAMPLES The present invention will be described below with reference to Examples, but these Examples do not limit the present invention in any way. In addition, the elastic modulus in Examples was evaluated by dynamic elastic modulus, and each physical property of the residue was measured by the following method.

密度: JIS  K  7112A法およびC法に準
拠1、て測定l−7、求めた。
Density: Measured 1-7 according to JIS K 7112A method and C method.

発泡倍率:発泡成形物の密度を非発池成形物の密度で除
した値で表1.た。
Expansion ratio: The value obtained by dividing the density of the foamed molded product by the density of the non-foamed molded product, as shown in Table 1. Ta.

動的弾性率および内部損失:東洋ボールドウィン製バイ
プロンL)L)[lEAを用いて、周波数110Hz 
、 230℃の条件にて動的弾性率(窃および内部損失
(tanδ)を測定し求めた。
Dynamic elastic modulus and internal loss: Toyo Baldwin Bipron L) L) [Using lEA, frequency 110 Hz
The dynamic elastic modulus (theft and internal loss (tan δ)) were measured and determined at 230°C.

実施例1および実施例2 メルトフローレート(230℃、21609)159/
10分のホモポリプロピレンに重量平均フレーク径が2
30μであ、b、xi平均アスペクト比が65である金
マイカ(スジライトマイカ150−8%印クりレ製)を
表1に示す割合で混合し、押出機で溶融混練することに
ようペレットを得た。このペレットを射出成形法により
、試験片を作製し、該試験片を用いて密度、弾性率、内
部損失を測定し結果を表1に示す。
Example 1 and Example 2 Melt flow rate (230°C, 21609) 159/
10 minutes of homopolypropylene with a weight average flake diameter of 2
Gold mica (Sujirite Mica 150-8% manufactured by Kurire Co., Ltd.) having a diameter of 30μ and an average b, xi aspect ratio of 65 was mixed in the proportions shown in Table 1, and melted and kneaded in an extruder to form pellets. I got it. A test piece was prepared from this pellet by an injection molding method, and the density, elastic modulus, and internal loss were measured using the test piece. The results are shown in Table 1.

実施例3 実施例1において、ウオラ・ストナイト(ケモリツ1−
8−3、丸和バイオケミカル■製)を表1に示す割合で
配合する以外は同様にして試験片を作製し、密度、弾性
率、内部損失を測定した。結果を表1に示す。
Example 3 In Example 1, Uora stonite (Kemoritsu 1-
8-3, manufactured by Maruwa Biochemical (■)) in the proportions shown in Table 1, test pieces were prepared in the same manner as above, and the density, elastic modulus, and internal loss were measured. The results are shown in Table 1.

実施例4 実施例1において、金マイカの代わbに重量平均フレー
ク径が20μであう、重蚤平均アスペクト比が40であ
る白マイカ(−クラレ#りを用いる以外は同様にして試
験片を作製し、密度、弾性率、内部損失を測定した。結
果を表1に示す。
Example 4 In Example 1, a test piece was prepared in the same manner as in Example 1, except that white mica (-Kuraray #2) having a weight average flake diameter of 20 μ and an average aspect ratio of 40 was used instead of gold mica. , density, elastic modulus, and internal loss were measured.The results are shown in Table 1.

実施例5 実施例1において、低温耐衝撃ポリプロピレン(J−8
1sHK、宇部興産■製)、重情平均フレーク径が20
μであり、重贋平均アスペクト比が40である白マイカ
およびウオラストナイトヶ表1に示す割合で混合する以
外は同様にして試験片を作製し、密度1弾性率、内部損
失を測定1.た。
Example 5 In Example 1, low temperature impact resistant polypropylene (J-8
1sHK, manufactured by Ube Industries), average flake diameter is 20
A test piece was prepared in the same manner except that white mica and wollastonite, which have an average particle diameter of 40 μ and an average aspect ratio of 40, were mixed in the proportions shown in Table 1, and the density, elastic modulus, and internal loss were measured. Ta.

結果を表1に示す。The results are shown in Table 1.

実施例6 実施例1において、メルトフローレート301/10分
のホモポリプロピレン、エチレン−エチルアクリレート
共重合体(MB87n、日本ユニカー■製、共重合率4
0重量遺憾および重量平均フレーク径が650μであう
%It(を平均アスペクト比が90である金マイカを用
いる以外は同様にして試験片を作製し、密度、弾性率、
内部損失を測定した。結果を表1に示す。
Example 6 In Example 1, homopolypropylene with a melt flow rate of 301/10 minutes, ethylene-ethyl acrylate copolymer (MB87n, manufactured by Nippon Unicar ■, copolymerization rate 4)
Test specimens were prepared in the same manner except that gold mica with an average aspect ratio of 90 was used, and the density, elastic modulus,
Internal loss was measured. The results are shown in Table 1.

比較例1〜5 実施例1において、メルトフローレート152/10分
のホモポリプロピレン、白マイカおよびウオラストナイ
トを表1に示す割合で配合する以外は同様にして試験片
を作製し、密度1弾性率、内部損失を測定した。桔釆を
filK示す。
Comparative Examples 1 to 5 Test pieces were prepared in the same manner as in Example 1, except that homopolypropylene with a melt flow rate of 152/10, white mica, and wollastonite were blended in the proportions shown in Table 1. The rate and internal loss were measured. Show the box.

実施例1〜6で得られた樹脂組成物よりなる成形物に比
較し、弾性率および比弾性率が劣っていた。
Compared with the molded products made of the resin compositions obtained in Examples 1 to 6, the elastic modulus and specific elastic modulus were inferior.

実施例7 実施例1において、ホモポリプロピレンの代ワbにアク
リル酸変性ポリプロピレン(東燃ポリプロc−soox
、東燃石油化学■製)を用いる以外は同様にして試験片
を作製し、密度、弾性率、内部損失を測定した。結果を
表1に示す。
Example 7 In Example 1, acrylic acid-modified polypropylene (Tonen Polypropylene C-SOOX) was substituted for homopolypropylene b.
A test piece was prepared in the same manner except that a sample (manufactured by Tonen Petrochemical Co., Ltd.) was used, and the density, elastic modulus, and internal loss were measured. The results are shown in Table 1.

実施例8および9 実施例7において、発泡剤(グイグローP E 111
20、大日本精化■製)を樹脂組成物100重量部に対
して5重量部添加させることによ91.1倍(実施例8
)、1.4倍(実施例9)に発泡させる以外は同様にし
て試験片を作興し、密度1弾性率、内部損失を測定した
。結果を表1に示す。
Examples 8 and 9 In Example 7, blowing agent (GuiGlo P E 111
20, manufactured by Dainippon Seika ■) to 100 parts by weight of the resin composition, 91.1 times (Example 8)
), a test piece was prepared in the same manner except that it was foamed 1.4 times (Example 9), and the density 1 elastic modulus and internal loss were measured. The results are shown in Table 1.

実施例10 実施例8において、無機充填材としてウオラストナイト
を添加する以外は同様にして試験片を作製し、密度1弾
性率、内部損失を測定した。結果を表1に示す。
Example 10 A test piece was prepared in the same manner as in Example 8 except that wollastonite was added as an inorganic filler, and the density 1 elastic modulus and internal loss were measured. The results are shown in Table 1.

実施例11 実施例1Oにおいて、発泡倍率を変える以外は同様にし
て試験片を作製し、密度1弾性率、内部損失を測定した
。結果を表1に示す。
Example 11 A test piece was prepared in the same manner as in Example 1O except that the expansion ratio was changed, and the density 1 elastic modulus and internal loss were measured. The results are shown in Table 1.

以下令白 〔発明の効果〕 本発明によれば、高弾性率および高内部損失を有し、か
つ軽拉化された成形物を得るためのポリプロピレン系樹
脂組成物が提供される。
[Effects of the Invention] According to the present invention, a polypropylene resin composition for obtaining a molded article having a high elastic modulus and a high internal loss and having a light abrasion is provided.

Claims (1)

【特許請求の範囲】[Claims]  ポリプロピレン系樹脂および重量平均フレーク径が1
0〜700μであり、重量平均アスペクト比が10以上
であるマイカ3〜15重量%を必須成分とする樹脂組成
物であつて、マイカを含めた無機充填材の含有率が20
重量%以下であることを特徴とするポリプロピレン系樹
脂組成物。
Polypropylene resin and weight average flake diameter of 1
A resin composition containing 3 to 15% by weight of mica having a weight average aspect ratio of 0 to 700μ and a weight average aspect ratio of 10 or more, the content of inorganic fillers including mica being 20% by weight.
% by weight or less.
JP32516389A 1989-12-14 1989-12-14 Polypropylene resin composition Expired - Fee Related JP2843391B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32516389A JP2843391B2 (en) 1989-12-14 1989-12-14 Polypropylene resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32516389A JP2843391B2 (en) 1989-12-14 1989-12-14 Polypropylene resin composition

Publications (2)

Publication Number Publication Date
JPH03185038A true JPH03185038A (en) 1991-08-13
JP2843391B2 JP2843391B2 (en) 1999-01-06

Family

ID=18173722

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32516389A Expired - Fee Related JP2843391B2 (en) 1989-12-14 1989-12-14 Polypropylene resin composition

Country Status (1)

Country Link
JP (1) JP2843391B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0585832U (en) * 1992-04-15 1993-11-19 東和産業株式会社 Plastic moldings
EP0962488A4 (en) * 1997-12-09 1999-12-08
CN112778648A (en) * 2021-01-28 2021-05-11 武汉瑞琪尔泰科技有限公司 Low-shrinkage lightweight modified PP composite material and preparation method and application thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0585832U (en) * 1992-04-15 1993-11-19 東和産業株式会社 Plastic moldings
EP0962488A4 (en) * 1997-12-09 1999-12-08
CN112778648A (en) * 2021-01-28 2021-05-11 武汉瑞琪尔泰科技有限公司 Low-shrinkage lightweight modified PP composite material and preparation method and application thereof

Also Published As

Publication number Publication date
JP2843391B2 (en) 1999-01-06

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