JPS59176340A - Ultra-high-molecular-weight polyethylene resin composition having improved resistance to impact and wear - Google Patents

Ultra-high-molecular-weight polyethylene resin composition having improved resistance to impact and wear

Info

Publication number
JPS59176340A
JPS59176340A JP5116283A JP5116283A JPS59176340A JP S59176340 A JPS59176340 A JP S59176340A JP 5116283 A JP5116283 A JP 5116283A JP 5116283 A JP5116283 A JP 5116283A JP S59176340 A JPS59176340 A JP S59176340A
Authority
JP
Japan
Prior art keywords
ultra
weight polyethylene
molecular weight
impact
powder
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
JP5116283A
Other languages
Japanese (ja)
Other versions
JPS647617B2 (en
Inventor
Tadao Matsuo
松尾 唯男
Fumio Matsuoka
松岡 文男
Nobuo Yokota
横田 伸夫
Masaaki Yamamoto
正明 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.)
Mitsuboshi Belting Ltd
Original Assignee
Mitsuboshi Belting 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 Mitsuboshi Belting Ltd filed Critical Mitsuboshi Belting Ltd
Priority to JP5116283A priority Critical patent/JPS59176340A/en
Publication of JPS59176340A publication Critical patent/JPS59176340A/en
Publication of JPS647617B2 publication Critical patent/JPS647617B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled resin compsn. which gives moldings having a coefficient of static friction approximately equal to that of ultra-high-molecular- weight polyethylene homopolymer molding and excellent resistance to impact and wear, by blending an org. peroxide and vulcanized rubber powder in specified quantities. CONSTITUTION:0.004-0.2pts.wt. org. peroxide (A) having a half life temp. of 10hr at 90-135 deg.C, such as dicumyl peroxide, and 3-100pts.wt. vulcanized rubber powder (B), (e.g. powder having a particle size of 1mm. or below formed when rubber goods such as tire or belt are grinded) are blended with 100pts.wt. ultra- high-molecular-weight polyethylene powder (C) (viscosity-average MW: 1,000,000 or above, light scattering average MW: 3,000,000 or above).

Description

【発明の詳細な説明】 本発明は耐衝撃摩耗特性を改善する超高分子量ポリエチ
レン樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to ultra-high molecular weight polyethylene resin compositions that have improved impact and wear properties.

従来、粘度法による平均分子量が100万以上、光散乱
法による平均分子量が300万以上の超高分子量ポリエ
チレンは、通常のポリエチレン(平均分子量が粘度法で
約3万程度まで、光散乱法で約60万程度まで)に比べ
耐摩擦摩耗性、低温特性、耐衝撃性、ストレス・クラン
キングに対する抵抗性などの種々の特性に優れており、
主な用途として自己潤滑性、低摩擦係数で耐摩擦摩耗特
性が要求される軸受、歯車、ローラー、ガイドレールな
どとして、また非粘着性、低摩擦係数でブリッジなどを
防ぎ、かつ耐摩耗性が要求されるホッパー、シュートな
どのライニング用として有用であったが、耐衝撃摩耗特
性が比較的低いため径の大きい粒子(砂利、生コン等)
が落下する部分のライニング用などでは摩耗が激しいと
いう難点があった・ 従来、上記のような耐衝撃摩耗特性を要求される用途に
は、ポリウレタン、ゴムなどの弾性を有した材料が用い
られてきたが、この場合摩擦係数そこで、本発明者等は
超高分子量ポリエチレン樹脂単独成形物と同程度の静摩
擦係数を有し、耐衝撃摩耗特性に優れた超高分子量ポリ
エチレン樹脂組成物を得ることを目的として鋭意検討し
た結果、超高分子量ポリエチレンに加硫ゴム粉末及びイ
〒1幾過酸化物を配合することにより目的を達成した。
Conventionally, ultra-high molecular weight polyethylene, which has an average molecular weight of 1 million or more by the viscosity method and 3 million or more by the light scattering method, has been used to produce ultra-high molecular weight polyethylene (with an average molecular weight of up to about 30,000 by the viscosity method and about 30,000 by the light scattering method). 600,000), it has excellent properties such as friction and wear resistance, low temperature properties, impact resistance, and resistance to stress and cranking.
Main uses include bearings, gears, rollers, guide rails, etc. that require self-lubricating properties, low friction coefficients, and friction and wear resistance, and non-adhesive, low friction coefficients that prevent bridging and wear resistance. It was useful for lining hoppers, chutes, etc., as required, but because of its relatively low impact abrasion resistance, large-diameter particles (gravel, ready-mixed concrete, etc.)
It has had the disadvantage of severe abrasion when used as linings for areas where objects fall. Conventionally, elastic materials such as polyurethane and rubber have been used for applications that require impact and abrasion resistance as described above. However, in this case, the coefficient of friction was the same. Therefore, the present inventors set out to obtain an ultra-high molecular weight polyethylene resin composition that had a static friction coefficient comparable to that of a molded ultra-high molecular weight polyethylene resin alone and had excellent impact and wear resistance properties. As a result of intensive study on the objective, the objective was achieved by blending vulcanized rubber powder and I-1 peroxide with ultra-high molecular weight polyethylene.

即−ら、本発明の特徴とするところは、超高分子量ポリ
エチレン100重量部に有機過酸化物0.004〜0.
2重量部および加硫コム粉を配合せしめる点にある。
Specifically, the present invention is characterized by adding 0.004 to 0.00 parts by weight of organic peroxide to 100 parts by weight of ultra-high molecular weight polyethylene.
2 parts by weight and vulcanized comb powder.

本発明でいう超高分子量ポリエチレンとは、市販の粉末
状超高分子量ポリエチレンで、平均分子量が粘度法で1
00万以上、光散乱法で300万以上のものを総称する
The ultra-high molecular weight polyethylene used in the present invention refers to commercially available powdered ultra-high molecular weight polyethylene, which has an average molecular weight of 1 as determined by the viscosity method.
1,000,000 or more, or 3,000,000 or more by light scattering method.

また、本発明でいう有機過酸化物とは、ジクミルパーオ
キサイド、2.5−ジメチル−2,5−シ(t−ブチル
パーオキシ)ヘキサンなどのジアルキルパーオキサ・イ
ド、1.1−ビス(t−ブチルパーオキシ) 3.3.
5− トリメチルシクロヘキサンなどのパーオキシケタ
ールなどの90’C〜135°Cの10時間半減期温度
を有する通常一般にポリエチレンの架橋に用いられる有
機過酸化物を総称していう。 そして、これらは超高分
子量ポリエチレンの粉末中への分散を考慮して粉末状が
望ましい。
In addition, the organic peroxide referred to in the present invention refers to dicumyl peroxide, dialkyl peroxide such as 2,5-dimethyl-2,5-di(t-butylperoxy)hexane, 1,1-bis (t-butylperoxy) 3.3.
A general term for organic peroxides, such as peroxyketals such as 5-trimethylcyclohexane, which have a 10-hour half-life temperature of 90'C to 135C and are commonly used for crosslinking polyethylene. These are preferably in powder form in consideration of dispersion in the ultra-high molecular weight polyethylene powder.

有機過酸化物の添加量は超高分子量ポリエチレンの粉末
100重量部に対し、0.004〜0,2重6量部、好
ましくは0.02〜0.2重量部である。
The amount of organic peroxide added is 0.004 to 0.2 parts by weight, preferably 0.02 to 0.2 parts by weight, per 100 parts by weight of the ultra-high molecular weight polyethylene powder.

0、004重量部以下だと耐摩耗性の向上が少なく、0
.2重量部以上だと動摩擦係数が大きくなることが知ら
れている。
If it is less than 0.004 parts by weight, the improvement in wear resistance will be small;
.. It is known that when the amount is 2 parts by weight or more, the coefficient of dynamic friction increases.

また、本発明でいう加硫ゴム粉とは、タイヤ、ヘルド等
のゴム製品を研磨する時に発生するゴム粉など、粒子径
1鮨程度あるいはそれ以下の加硫ゴムの粉末のことであ
る。加硫ゴム粉の配合量は図に示した静摩擦係数の値か
ら超高分子量ポリエチレンの粉末10(lffiffi
部に対して3〜100重量部が好ましい。
Further, the vulcanized rubber powder as used in the present invention refers to vulcanized rubber powder with a particle size of about 1 sushi or less, such as rubber powder generated when polishing rubber products such as tires and healds. The blending amount of the vulcanized rubber powder is determined from the value of the static friction coefficient shown in the figure.
3 to 100 parts by weight is preferred.

また、本発明の超高分子量ポリエチレン樹脂組成物は、
上記添加剤以外に通常一般に樹脂に混入して用いられる
補強剤、増量剤、添加剤などを含んでもよいことは勿論
である。
Moreover, the ultra-high molecular weight polyethylene resin composition of the present invention is
It goes without saying that in addition to the above-mentioned additives, reinforcing agents, extenders, additives, etc. that are commonly mixed into resins may also be included.

更に、この粉末状超高分子量ポリエチレン樹脂組成物の
成形に際しては、通常の超高分子量ポリエチレン粉末の
成形法と同様、圧縮成形、ラム押出成形、射出成形など
により、板、棒、パイプ、異形品などを製造することが
できる。
Furthermore, when molding this powdered ultra-high molecular weight polyethylene resin composition, it can be molded into plates, rods, pipes, and irregularly shaped products by compression molding, ram extrusion molding, injection molding, etc. in the same way as the usual molding methods for ultra-high molecular weight polyethylene powder. etc. can be manufactured.

以下、本発明を実施例によって詳述するが、本発明がこ
れのみに限定されるものでないことは云うまでもない。
EXAMPLES The present invention will be described in detail below with reference to examples, but it goes without saying that the present invention is not limited to these examples.

実施例 超高分子量ポリエチレンの粉末[ヘキスト社製、11o
stalen GUR412コに対し、炭酸カルシュラ
ムで40重素置に希釈したジクミルパーオキサイド[日
本油脂0勾製、パークミルD−401およびタイヤ研磨
ゴム粉をそれぞれ表1に示す混合割合でヘンシェルミキ
号−を用い800 rpmで20分間混合し、粉末状超
高分子量ポリエチレン樹脂組成物を得た。この粉末状超
高分子量ポリエチレン樹脂組成物を所定!(370g>
秤取し、仮作成用金型(内面180nva×22 f)
+nm)中で37トンプレスを用いて(80〜100 
kg/cボ)×10分子備圧縮を行った後、プレス熱盤
を230℃に設定し、20〜40kg/cfflの面圧
をかけ65分加熱し、その後80〜100 kg/cn
lO面圧をかけ30分冷却し、厚さ10m+nX1W1
78mmX横218m+nの坂を成形し、この坂から1
00+nmX 220+Rmの坂を切出し、静摩擦係数
および衝撃摩耗用の試験片とした。静摩擦係数は試料板
上に鉄片(接触面積18cJ、重ff1123g)を置
き、鉄片がすべり出す時の試料板の傾斜角を測定するこ
とにより求めた。
Example Ultra-high molecular weight polyethylene powder [manufactured by Hoechst, 11o
To stalen GUR412, dicumyl peroxide diluted to 40% with calcium carbonate [NOF 0 grade, Percmill D-401, and tire polishing rubber powder were added to Henschel Miki No. 1 at the mixing ratios shown in Table 1. The mixture was mixed for 20 minutes at 800 rpm to obtain a powdered ultra-high molecular weight polyethylene resin composition. This powdered ultra-high molecular weight polyethylene resin composition is prescribed! (370g>
Weighing and temporary production mold (inner surface 180nva x 22f)
+nm) using a 37 ton press (80-100
After compression with 10 molecules (kg/c), set the press heating plate to 230℃, apply a surface pressure of 20 to 40 kg/cffl and heat for 65 minutes, then 80 to 100 kg/cn.
Apply lO surface pressure and cool for 30 minutes, thickness 10m+nX1W1
Form a slope of 78 mm x 218 m + n, and from this slope 1
A slope measuring 00+nm x 220+Rm was cut out and used as a test piece for static friction coefficient and impact wear. The coefficient of static friction was determined by placing an iron piece (contact area 18 cJ, weight ff 1123 g) on a sample plate and measuring the angle of inclination of the sample plate when the iron piece began to slide.

この傾斜角をθとするとtanθが 静摩擦係数になる
。その結果を図に示す。
If this angle of inclination is θ, then tanθ is the coefficient of static friction. The results are shown in the figure.

次に耐衝撃摩耗試験は生コンクリート用ホ・ツバ−内に
各試験片を貼り付は試験開始後1ク一月、1゜5ケ月、
2ケ月および以後1ケ月毎の摩耗変化を目視により確認
した。なお、生コンクリートの投入量は1ハツチ1.5
Mで約380パ・ノチ/日であり、含まれる砂利の粒子
径は0.15〜40mm、落下高さは850 mmであ
る。また生コンクリ−1−のおおよその配合割合は砂(
粒子径0.15〜5IIIIII):砂利(粒子径5〜
40mm):セメント:水−5:1:1:2である。こ
の試験結果を第2表にしめす。
Next, for the impact abrasion test, each test piece was pasted inside the hot spring for fresh concrete for 1 month, 1.5 months after the start of the test.
Changes in wear were visually confirmed for 2 months and every month thereafter. In addition, the amount of fresh concrete input is 1 hatch 1.5
M is approximately 380 pa-noti/day, the particle size of the gravel contained is 0.15 to 40 mm, and the falling height is 850 mm. In addition, the approximate mixing ratio of ready-mixed concrete 1- is sand (
Particle size 0.15~5III): Gravel (particle size 5~
40 mm): cement: water - 5:1:1:2. The test results are shown in Table 2.

(以下、余白) 第1表 (重量部) (注)有機過酸化物配合割合の内()は有効有機過酸化
物割合に換算したものを示す。
(Hereafter, blank space) Table 1 (parts by weight) (Note) The number in parentheses in the organic peroxide blending ratio shows the value converted to the effective organic peroxide ratio.

第2表 ごの結果から明らかなように本発明の組成物は超高分子
量ポリエヂレン単独成形物(比較例1)に比べ耐衝撃摩
耗特性にすぐれている。また図かられかるように超高分
子量ポリエチレン100重量部に対し、タイヤ研磨ゴム
粉が10重量部以下の配合組成物では、静摩擦係数が超
高分子量ポリエチレン単独成形物と同程度あるいはそれ
以下の値十分適用できるものである。
As is clear from the results shown in Table 2, the composition of the present invention has superior impact and wear resistance properties compared to the molded product made from ultra-high molecular weight polyethylene alone (Comparative Example 1). Furthermore, as can be seen from the figure, in a compounded composition in which the tire polishing rubber powder is 10 parts by weight or less per 100 parts by weight of ultra-high molecular weight polyethylene, the coefficient of static friction is the same as or lower than that of a molded product of ultra-high molecular weight polyethylene alone. It is fully applicable.

【図面の簡単な説明】[Brief explanation of the drawing]

図は本発明の実施例に係るものであってタイヤ研磨ゴム
粉の添加量と静摩擦係数の関係を示すグラフである。 特許出願人 三・7星ベルト株式会社
The figure relates to an example of the present invention and is a graph showing the relationship between the amount of tire polishing rubber powder added and the coefficient of static friction. Patent applicant San-Seven Star Belt Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 粘度法による平均分子量が100万以上、光散乱法によ
る平均分子量が300万以上の超高分子量ポリエチレン
粉末100重量部に有機過酸化物0.004〜0,2重
量部及び加硫ゴム粉を配合してなることを特徴とする耐
衝撃摩耗特性を改善する超高分子量ポリエチレン樹脂組
成物
0.004 to 0.2 parts by weight of organic peroxide and vulcanized rubber powder are blended with 100 parts by weight of ultra-high molecular weight polyethylene powder with an average molecular weight of 1 million or more by a viscosity method and an average molecular weight of 3 million or more by a light scattering method. An ultra-high molecular weight polyethylene resin composition that improves impact and wear resistance characteristics.
JP5116283A 1983-03-25 1983-03-25 Ultra-high-molecular-weight polyethylene resin composition having improved resistance to impact and wear Granted JPS59176340A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5116283A JPS59176340A (en) 1983-03-25 1983-03-25 Ultra-high-molecular-weight polyethylene resin composition having improved resistance to impact and wear

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5116283A JPS59176340A (en) 1983-03-25 1983-03-25 Ultra-high-molecular-weight polyethylene resin composition having improved resistance to impact and wear

Publications (2)

Publication Number Publication Date
JPS59176340A true JPS59176340A (en) 1984-10-05
JPS647617B2 JPS647617B2 (en) 1989-02-09

Family

ID=12879124

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5116283A Granted JPS59176340A (en) 1983-03-25 1983-03-25 Ultra-high-molecular-weight polyethylene resin composition having improved resistance to impact and wear

Country Status (1)

Country Link
JP (1) JPS59176340A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62172061A (en) * 1986-01-23 1987-07-29 アクゾ・ナ−ムロ−ゼ・フエンノ−トシヤツプ High-molecular crosslinking composition
JPS6335452U (en) * 1986-08-27 1988-03-07

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62172061A (en) * 1986-01-23 1987-07-29 アクゾ・ナ−ムロ−ゼ・フエンノ−トシヤツプ High-molecular crosslinking composition
JPS6335452U (en) * 1986-08-27 1988-03-07
JPH0711799Y2 (en) * 1986-08-27 1995-03-22 大日本印刷株式会社 Spray nozzle

Also Published As

Publication number Publication date
JPS647617B2 (en) 1989-02-09

Similar Documents

Publication Publication Date Title
US5385953A (en) Microcellular polyurethane composite
US4645791A (en) Environmentally durable elastomer composition with excellent low temperature dynamic properties
US4427831A (en) Rubber materials having excellent grip on ice
GB2364708A (en) Pre-coated rubber crumb for composites
JPS59176340A (en) Ultra-high-molecular-weight polyethylene resin composition having improved resistance to impact and wear
US3578728A (en) Liquid unsaturated polyesters and polyester urethanes containing cross-linked particles of the same resins
US3468838A (en) Silicone rubber materials
US3259598A (en) Vulcanizing agent prepared from sulfur, linseed oil and styrene
US1111284A (en) Plastic composition.
KR102074237B1 (en) Bio plastic composition comprising wheat bran and Bio plastic film using therefrom
JP2504841B2 (en) Rubber mat manufacturing method
US2814604A (en) Compositions comprising diisocyanatelinked elastomers and silicon dioxide
US2858283A (en) Method of making textile fiber drafting elements containing animal glue, a rubber, and a surface-active material
CN109575577A (en) A kind of wood imitation structure water lubricating bearing material
US1302463A (en) Vulcanizable composition of matter having comminuted leather as a base and method of preparing same.
US1897626A (en) Method of producing rubber articles
KR101902203B1 (en) Composition of flame retardant urethane liner and preparing method thereof
US674872A (en) Material applicable for valve-packing or other purposes.
US655131A (en) Wurtzilite method and product.
US3084130A (en) Dry cold molding composition containing thermosetting resin binder and hydrated mineral absorbent
US1884118A (en) Process of reconditioning old rubber
RU2111989C1 (en) Polymer composition
US1259806A (en) Plastic compositon.
JPH0539384A (en) Rubber composition and its manufacture
US3296185A (en) High impact hard rubber compound and method of making same