JPS61204245A - Polyolefin composition - Google Patents

Polyolefin composition

Info

Publication number
JPS61204245A
JPS61204245A JP4357385A JP4357385A JPS61204245A JP S61204245 A JPS61204245 A JP S61204245A JP 4357385 A JP4357385 A JP 4357385A JP 4357385 A JP4357385 A JP 4357385A JP S61204245 A JPS61204245 A JP S61204245A
Authority
JP
Japan
Prior art keywords
mica
weight
polyolefin
composition
parts
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
Application number
JP4357385A
Other languages
Japanese (ja)
Inventor
Kiyotada Narukawa
鳴川 喜代忠
Takashi Yamahata
山畑 孝
Noboru Yamamoto
登 山本
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.)
Tonen General Sekiyu KK
Original Assignee
Toa Nenryo Kogyyo KK
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 Toa Nenryo Kogyyo KK filed Critical Toa Nenryo Kogyyo KK
Priority to JP4357385A priority Critical patent/JPS61204245A/en
Publication of JPS61204245A publication Critical patent/JPS61204245A/en
Pending legal-status Critical Current

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  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Organic Insulating Materials (AREA)

Abstract

PURPOSE:To obtain the titled composition having excellent heat-resistance and voltage-resistance and suitable for the distributor cap and rotor of an automobile, by adding a small amount of a foaming agent, a silane coupling agent and an organic peroxide to a composition composed of a polyolefin and mica at a specific ratio. CONSTITUTION:The objective composition is produced by compounding (A) 100pts.wt. of a composition composed of (i) 95-40wt%, preferably 90-40% polyolefin (preferably propylene polymer) and (ii) 5-60%, preferably 10-60% mica [preferably phlogopite of formula K2Mg6(Si3Al)2O20(OH)4 or muscovite of formula K2Al4(Si3Al)2O20(OH)4] with (B) 0.05-0.5pts. of a foaming agent (e.g. azodicarbonamide), (C) 0.5-5pts. (based on 100pts. of mica) of a silane coupling agent (e.g. triethoxypropylamino-silane) and (D) 0.01-1pt. (based on 100pts. of mica) of an organic peroxide (e.g. di-t-butyl peroxide).

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、ポリオレフィンに無機充填剤及び発泡剤を配
合した耐電圧性組成物に関し、特にマイカ、発泡剤を配
合した自動車のディストリビュータ・キャップ及びロー
ター用途に適した耐熱性、耐電圧性が良好なポリオレフ
ィン組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a voltage-resistant composition containing polyolefin, an inorganic filler, and a blowing agent, and in particular, use in automobile distributor caps and rotors containing mica and a blowing agent. The present invention relates to a polyolefin composition having good heat resistance and voltage resistance suitable for

従来の技術 従来自動車等の電装部品の構造材料、絶縁材料用として
ポリエステル樹脂、フェノール樹脂、ポリオレフィン樹
脂などに無機充填剤を配合して、耐アーク性、耐トラツ
キング特性を付与する試みがなされている。しかしなが
ら最近の自動車用のディストリビュータ・キャップ及び
ロータに要求される性能は新しい公害防止技術及びエン
ジンの高性能化へ対厄するためによシ高い耐電圧性及び
高電圧がかかることにより上昇する熱に対する耐久性が
必要とされてきている。
Conventional technology Attempts have been made to add arc resistance and tracking resistance to polyester resins, phenolic resins, polyolefin resins, etc., by adding inorganic fillers to them for use as structural materials and insulating materials for electrical components such as automobiles. . However, the performance required of distributor caps and rotors for recent automobiles has increased in order to cope with new pollution prevention technology and higher engine performance, and to withstand higher voltage and to withstand the heat that increases due to the application of high voltage. Durability is becoming a necessity.

このために多量の無機充填剤を添加したり、成形品の肉
厚を厚くすることが行われているが、成形品の内部に空
隙が発生したり、成形品表面にひけが生じたりして、か
えって耐電圧性が悪(なる現像が生じている。無機充填
剤を添加し九り、成形品の肉厚を厚くすることによる成
形品のあばれ、ひけなどの発生を防止するために発泡成
形する技術が特開昭53−50251号、特開昭59−
20333号、特開昭59−22956号公報などに開
示されているが、いずれの技術も自動車のディストリビ
ュータ・キャップ及びロータ用途に適した耐電圧性、耐
熱性の良好なものは認識されずかつ得られていなかつ九
For this purpose, large amounts of inorganic fillers are added or the thickness of the molded product is made thicker, but this results in voids forming inside the molded product and sink marks on the surface of the molded product. However, in order to prevent the occurrence of cracks and sink marks on the molded product due to the addition of inorganic fillers and thickening of the wall thickness of the molded product, foam molding is used. The technology to do this is disclosed in JP-A-53-50251 and JP-A-59-
No. 20333, Japanese Unexamined Patent Publication No. 59-22956, etc., but none of these technologies have been recognized as having good voltage resistance and heat resistance suitable for use in automobile distributor caps and rotors. 9.

本発明は前記の問題即ち無機充填剤含有ポリオレフィン
組成物から成形物上製造する際に成形物内部に空隙の発
生を防止し、成形物表面のひけやそ9の発生を防止した
耐電圧性、耐熱性の良好な自動車用のディストリビュー
タ・キャップ及びロータを製造するためのポリオレフィ
ン組成物を提供することを目的とする。
The present invention solves the above-mentioned problem, that is, voltage resistance that prevents the generation of voids inside the molded product and prevents the occurrence of sink marks and crevices 9 on the surface of the molded product when producing the molded product from a polyolefin composition containing an inorganic filler. The object of the present invention is to provide a polyolefin composition for producing automobile distributor caps and rotors with good heat resistance.

問題点を解決するための手段 本発明者らは種々検討を行った結果、ポリオレフィンに
マイカを加え、シランカップリング剤および発泡剤の存
在下に架橋発泡成形することによって成形品内部の空隙
全防止し、耐電圧性および耐熱性を大幅に向上させるこ
とができる自動車用のディストリビュータ・キャップお
よびロータに適したポリオレフィン組成物を見出し本発
明を完成した。
Means for Solving the Problems The inventors conducted various studies and found that by adding mica to polyolefin and performing cross-linking foam molding in the presence of a silane coupling agent and a foaming agent, voids inside the molded product were completely prevented. The present invention was completed by discovering a polyolefin composition suitable for automotive distributor caps and rotors that can significantly improve voltage resistance and heat resistance.

すなわち、本発明はポリオレフイン95S40重量%と
マイカ5〜60重量%の組成物100重量部に対して発
泡剤を0,05〜0.5重量部、マイカ100重量部に
対してシランカップリング剤を0,5〜5重量部および
有機過酸化物0.01〜1重量部とを配合してなること
を特徴とする耐電圧性ポリオレフィン組成物である。
That is, the present invention uses 0.05 to 0.5 parts by weight of a blowing agent to 100 parts by weight of a composition containing 40% by weight of polyolefin 95S and 5 to 60% by weight of mica, and a silane coupling agent to 100 parts by weight of mica. This is a voltage-resistant polyolefin composition characterized in that it contains 0.5 to 5 parts by weight and 0.01 to 1 part by weight of an organic peroxide.

以下本発明の構成について詳細に説明する。The configuration of the present invention will be explained in detail below.

本発明におけるポリオレフィンとしては高・中・低圧法
ポリエチレン、ポリプロピレン、ポリブテン−1等のポ
リマー、エチレン−プロピレン共重合体、エチレン−酢
酸ビニル共重合体、エチレン−アクリル酸共重合体、エ
チレン−a・オレフィン共重合体等のオレフィン系エラ
ストマーであり、これらのポリマー、エラストマーの1
種または2種以上の混合物をいう。これら重合体のうち
でポリプロピレン、プロピレン−エチレンランダムもし
くはブロック共重合体、プロピレン−1−ブテン共重合
体などのプロピレン系重合体において特に効果が著しく
、組成物中に95〜40重食%の範囲で用いるのが好ま
しく、特に90−400重量部の範囲で用いるのが好ま
しい。また上記オレフィン系樹脂に変性ポリオレフィン
塩素化ポリエチレン、38R。
Polyolefins used in the present invention include high-, medium-, and low-pressure polyethylene, polypropylene, polymers such as polybutene-1, ethylene-propylene copolymers, ethylene-vinyl acetate copolymers, ethylene-acrylic acid copolymers, ethylene-a, It is an olefin elastomer such as an olefin copolymer, and one of these polymers and elastomers
A species or a mixture of two or more species. Among these polymers, propylene-based polymers such as polypropylene, propylene-ethylene random or block copolymers, and propylene-1-butene copolymers are particularly effective, and are present in the composition in a range of 95 to 40%. It is preferably used in an amount of 90 to 400 parts by weight. In addition, modified polyolefin chlorinated polyethylene, 38R is added to the above olefin resin.

ポリイノブチレン、ポリブタジェン等を変性剤として添
加してもよい。その他必要に応じて着色剤、核剤、老化
防止剤、紫外線吸収剤、難燃剤、架橋助剤、発泡助剤、
滑剤などの添加剤を加えても良い。
Polyinobutylene, polybutadiene, etc. may be added as a modifier. Other colorants, nucleating agents, anti-aging agents, ultraviolet absorbers, flame retardants, crosslinking aids, foaming aids,
Additives such as lubricants may also be added.

本発明において配合するマイカとしては平均粒子径1〜
500μの白マイカ、紅マイカ、ソーダマイカ、絹マイ
カ、バナジンマイカ、イライト等の白マイカ系マイカや
黒マイカ、金マイカ、チンワルドマイカ等の黒マイカ系
マイカを挙げることができ、中でも特に例えば構造式に
2Mg6(S4sA4)202o(OH)4で示される
金マイカや例えばに2A44(813A/)2Q2o(
OH)4で示される白マイカが好ましい。マイカの配合
量は5〜60重量%が好ましく、特に10〜60重量%
の範囲で使用するのが好ましい。60重量%を越えると
成形性が悪くなり、5重量%未満では耐電性が悪くなる
The average particle size of the mica to be blended in the present invention is 1 to 1.
Examples include white mica such as 500μ white mica, red mica, soda mica, silk mica, vanadium mica, and illite, and black mica such as black mica, gold mica, and Chinwald mica, among which, for example, structural formula For example, gold mica shown as 2Mg6(S4sA4)202o(OH)4 or 2A44(813A/)2Q2o(
White mica represented by OH)4 is preferred. The blending amount of mica is preferably 5 to 60% by weight, particularly 10 to 60% by weight.
It is preferable to use it within the range of . If it exceeds 60% by weight, moldability will deteriorate, and if it is less than 5% by weight, electrical resistance will deteriorate.

本発明におけるシランカップリング剤とバ一般式R’5
i(OR2)、で示される有機シラン化合物であり、R
1は酸、酸無水物あるいはそのエステル類と親和性のあ
る極性官能基を有するアルキル基又はアリール基である
。R1の具体的なものとしては、例えばr−アミノプロ
ピル、u−p−(アミノエチル)r−アミノプロピル、
r−フレイドプロピル、r−グリシドキシプロビル、−
一(3,4−エポキシクロへキシル〕エチル、“r−メ
ルカプトプロピル、バラアミノフェニルなどがあげられ
る。R2はアルキル基又はアリール基であシ、その具体
的なものとしては例えば、メチル、エチル、プロピル、
ブチル、β−メト中クジエチルフェニルなどがあげられ
る。これらの有機シラン化合物のうちでは、トリエトキ
シプロピルアミノシラン、r−ウレイドプロピルトリエ
トキシシランなどが好ましい。有機シラン化合物の配合
量は添加したマイカ100重量部に対して0.5〜5重
量部が好ましい。
Silane coupling agent in the present invention and general formula R'5
It is an organic silane compound represented by i(OR2), and R
1 is an alkyl group or an aryl group having a polar functional group having an affinity with acids, acid anhydrides, or esters thereof. Specific examples of R1 include r-aminopropyl, up-(aminoethyl)r-aminopropyl,
r-freidopropyl, r-glycidoxyprovir, -
Examples include mono(3,4-epoxychlorohexyl)ethyl, r-mercaptopropyl, paraaminophenyl, etc. R2 is an alkyl group or an aryl group, and specific examples thereof include methyl, ethyl , propyl,
Examples include butyl, β-meth, and cudiethylphenyl. Among these organic silane compounds, triethoxypropylaminosilane, r-ureidopropyltriethoxysilane, and the like are preferred. The amount of the organic silane compound to be blended is preferably 0.5 to 5 parts by weight per 100 parts by weight of added mica.

本発明における有機過酸化物は加熱により分解してラジ
カルを発生する過酸化物で、たとえばジ−t−ブチルパ
ーオキサイド、ジクミルパーオキサイド、t−ブチルク
ミルパーオキサイド、α、αI−ビス(t−ブチルパー
オキシフp−ジインプロビルベンゼン、2,5−ジメチ
ル−2,5−ジ(t−ブチルパーオキシ〕ヘキサン、2
,5−ジメチル−2,5−ジ(t−ブチルパーオキシ)
ヘキシン−3などを1種または2s以上を用いる。必要
に応じて架橋助剤を用いても良い。有機過酸化物の配合
量はマイカ100重量部に対して0.01〜1重量部が
好ましい。
The organic peroxide used in the present invention is a peroxide that decomposes upon heating to generate radicals, such as di-t-butyl peroxide, dicumyl peroxide, t-butylcumyl peroxide, α, αI-bis(t -butylperoxyph p-diimprobylbenzene, 2,5-dimethyl-2,5-di(t-butylperoxy)hexane, 2
,5-dimethyl-2,5-di(t-butylperoxy)
One type or 2s or more of hexin-3 or the like is used. A crosslinking aid may be used if necessary. The amount of organic peroxide to be blended is preferably 0.01 to 1 part by weight per 100 parts by weight of mica.

本発明における発泡剤とは加熱により分解して比較的急
激にガスを発生する熱分解型発泡剤が好ましく、例えば
アゾジカルボンアミド、ヒドラジカルボンアミド、ジニ
トロンベンタメテレンテトラミン、 p、p′−オ牟シ
ビスベンゼンスルホニルヒドラジド等の1種又は2珈以
上の混合物である。発泡剤の配合量は目的とする発泡体
の倍率によって選択され得るが、本発明の発泡体ではポ
リオレフィン系樹脂組成物100重量部に対して0.0
5〜0.5重量部を添加するのが耐電圧性及び耐熱性を
発揮させるのに好ましい。
The blowing agent used in the present invention is preferably a thermally decomposable blowing agent that decomposes when heated and generates gas relatively rapidly, such as azodicarbonamide, hydradicarbonamide, dinitron bentametherenetetramine, p, p'-o It is one kind or a mixture of two or more such as bisbenzenesulfonyl hydrazide. The amount of the blowing agent can be selected depending on the desired expansion ratio of the foam, but in the foam of the present invention, it is 0.0 parts by weight per 100 parts by weight of the polyolefin resin composition.
It is preferable to add 5 to 0.5 parts by weight in order to exhibit voltage resistance and heat resistance.

本発明においては上記ポリオレフィンに上記マイカおよ
びシランカップリング剤、有機過酸化物、発泡剤さらに
必要に応じて他の添加剤を混合して各種押出機音用いて
造粒する。勿論この工程は有機過酸化物および発泡剤の
分解温度より20−50℃程低い樹脂温度で造粒する必
要がある。成形品は得られたペレットから射出成形、押
出成形などで成形することができるが、各成分を混合し
たものから直接成形しても良い。
In the present invention, the above polyolefin is mixed with the above mica, a silane coupling agent, an organic peroxide, a blowing agent, and other additives as necessary, and granulated using various extruder noises. Of course, this step requires granulation at a resin temperature that is about 20-50°C lower than the decomposition temperature of the organic peroxide and blowing agent. A molded product can be molded from the obtained pellets by injection molding, extrusion molding, etc., but it may also be molded directly from a mixture of each component.

発泡成形についてはマスターバッチ法又はトライブレン
ド法のいづれを用いても良い。
For foam molding, either the masterbatch method or the triblend method may be used.

発明の効果 本発明のポリオレフィン組成物からの成形品は充填剤含
量が高いにもかかわらず均一な発泡体架橋構造が導入さ
れているため耐電圧性、耐熱性が良く自動車のディスト
リビュータ・キャップ及びロータのような高耐電圧を必
要とする用途に用いることができる。
Effects of the Invention Molded products made from the polyolefin composition of the present invention have a uniform cross-linked foam structure despite the high filler content, so they have good voltage resistance and heat resistance, and are suitable for automobile distributor caps and rotors. It can be used in applications that require high withstand voltage such as.

実施例 以下に本発明の実施例を示す。なお実施例における試験
法は次の通シである。
Examples Examples of the present invention are shown below. The test method in the examples is as follows.

1〕 耐電圧の測定(促進):12111厚さのテスト
ピースを周波数700 G/S、電圧25KV、温 度100℃で測定 2) 耐熱性     : Ai9TM D−648(
4,4g厚さのテスト ピース、264 psl で熱劣化温度()EDT) 全測定】 実施例1〜7、比較例1〜B ポリプロピレン(MI:20360重量%と白マイカ【
粒径27μ]40重量%からなる混合物100重量部に
トリエトキシグロビルアミノシラン、2,5−ジメチル
−2,5−ジ(t−ブチルパーオキシ)ヘキシン−3お
よびヒドラジカルボンアミドを表1に示す配合量でそれ
ぞれ添加し、高速ミキサーで混合し得られた混合物を2
軸混練機を用いてシリンダ一温度190−220℃で溶
融混線後造粒した。得られたペレットヲシリンダ一温度
250℃、射出圧力600kl/IB2  の射出条件
で試験片を成形し耐電圧および耐熱性を測定した。その
結果を表−1に示した。
1] Measurement of withstand voltage (promotion): Measure a test piece with a thickness of 12111 at a frequency of 700 G/S, a voltage of 25 KV, and a temperature of 100°C. 2) Heat resistance: Ai9TM D-648 (
4.4 g thick test piece, thermal deterioration temperature (EDT) at 264 psl All measurements] Examples 1 to 7, Comparative Examples 1 to B Polypropylene (MI: 20360% by weight and white mica [
Table 1 shows triethoxyglobylaminosilane, 2,5-dimethyl-2,5-di(t-butylperoxy)hexine-3, and hydradicarbonamide in 100 parts by weight of a mixture consisting of 40% by weight [particle size 27μ]. Add each amount in the blended amount and mix with a high speed mixer.
The mixture was melt mixed and granulated using a shaft kneader at a cylinder temperature of 190-220°C. The obtained pellets were molded into test pieces under injection conditions of a cylinder temperature of 250° C. and an injection pressure of 600 kl/IB2, and the withstand voltage and heat resistance were measured. The results are shown in Table-1.

なお、比較のためシランカップリング剤1発泡剤を用い
ない場合についても同様の評価を行い、その結果を表−
1jC併記した。
For comparison, the same evaluation was conducted for the case in which the silane coupling agent 1 and the blowing agent were not used, and the results are shown in the table below.
1jC was also written.

Claims (1)

【特許請求の範囲】 ポリオレフィン95−40重量%とマイカ 5−60重量%の組成物100重量部に対して発泡剤を
0.05〜0.5重量部、マイカ100重量部に対して
シランカップリング剤を0.5〜5重量部および有機過
酸化物0.01〜1重量部とを配合してなることを特徴
とする耐電圧性ポリオレフィン組成物。
Scope of Claims: 0.05 to 0.5 parts by weight of a blowing agent to 100 parts by weight of a composition containing 95 to 40% by weight of polyolefin and 5 to 60% by weight of mica, and a silane cup to 100 parts by weight of mica. A voltage-resistant polyolefin composition comprising 0.5 to 5 parts by weight of a ring agent and 0.01 to 1 part by weight of an organic peroxide.
JP4357385A 1985-03-07 1985-03-07 Polyolefin composition Pending JPS61204245A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4357385A JPS61204245A (en) 1985-03-07 1985-03-07 Polyolefin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4357385A JPS61204245A (en) 1985-03-07 1985-03-07 Polyolefin composition

Publications (1)

Publication Number Publication Date
JPS61204245A true JPS61204245A (en) 1986-09-10

Family

ID=12667488

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4357385A Pending JPS61204245A (en) 1985-03-07 1985-03-07 Polyolefin composition

Country Status (1)

Country Link
JP (1) JPS61204245A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6295330A (en) * 1985-10-21 1987-05-01 Kuraray Co Ltd Foamed thermoplastic resin article
JPS63213541A (en) * 1987-02-28 1988-09-06 Fujikura Ltd Electrical insulating composition
WO2011111696A1 (en) * 2010-03-08 2011-09-15 旭化成ケミカルズ株式会社 Foam composition, method for producing same, and foam
WO2013147148A1 (en) * 2012-03-30 2013-10-03 古河電気工業株式会社 Method for producing heat-resistant resin composition, heat-resistant resin composition produced by method for producing heat-resistant resin composition, and molded article using heat-resistant resin composition

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6295330A (en) * 1985-10-21 1987-05-01 Kuraray Co Ltd Foamed thermoplastic resin article
JPH0542975B2 (en) * 1985-10-21 1993-06-30 Kuraray Co
JPS63213541A (en) * 1987-02-28 1988-09-06 Fujikura Ltd Electrical insulating composition
WO2011111696A1 (en) * 2010-03-08 2011-09-15 旭化成ケミカルズ株式会社 Foam composition, method for producing same, and foam
CN102791782A (en) * 2010-03-08 2012-11-21 旭化成化学株式会社 Foam composition, method for producing same, and foam
US20120322905A1 (en) * 2010-03-08 2012-12-20 Yasuhiro Kusanose Foamable Composition, Process for Producing the Same and Foam
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