JPH02191650A - Self-lubricative styrenic resin composition - Google Patents
Self-lubricative styrenic resin compositionInfo
- Publication number
- JPH02191650A JPH02191650A JP27630488A JP27630488A JPH02191650A JP H02191650 A JPH02191650 A JP H02191650A JP 27630488 A JP27630488 A JP 27630488A JP 27630488 A JP27630488 A JP 27630488A JP H02191650 A JPH02191650 A JP H02191650A
- Authority
- JP
- Japan
- Prior art keywords
- styrenic resin
- resin composition
- self
- silicone oil
- pts
- 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
Links
- 239000011342 resin composition Substances 0.000 title claims abstract description 17
- 229920001890 Novodur Polymers 0.000 title claims abstract description 13
- 229920002545 silicone oil Polymers 0.000 claims abstract description 20
- 235000021355 Stearic acid Nutrition 0.000 claims abstract description 14
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims abstract description 14
- -1 stearate ester Chemical class 0.000 claims abstract description 14
- 239000008117 stearic acid Substances 0.000 claims abstract description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 12
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims abstract description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 21
- 229920005989 resin Polymers 0.000 claims description 18
- 239000011347 resin Substances 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 abstract description 5
- 239000004793 Polystyrene Substances 0.000 abstract description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 abstract description 3
- 238000004898 kneading Methods 0.000 abstract description 3
- 239000000203 mixture Substances 0.000 abstract description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 abstract description 3
- 229920001893 acrylonitrile styrene Polymers 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- 229920001296 polysiloxane Polymers 0.000 abstract description 2
- 229920002223 polystyrene Polymers 0.000 abstract description 2
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 abstract description 2
- 238000013329 compounding Methods 0.000 abstract 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 abstract 1
- 235000019441 ethanol Nutrition 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 238000000465 moulding Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 5
- 238000001746 injection moulding Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 229920007962 Styrene Methyl Methacrylate Polymers 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- ADFPJHOAARPYLP-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;styrene Chemical compound COC(=O)C(C)=C.C=CC1=CC=CC=C1 ADFPJHOAARPYLP-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、摺動性を与える為にスチレン系樹脂にシリコ
ーンオイルを含有させた自己潤滑性樹脂組成物に関する
。この組成物は射出成形時、高剪断力下にさらされたと
き成形品に生ずる黒条が発生しにくい特長をもっている
。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a self-lubricating resin composition in which a styrene resin contains silicone oil to provide sliding properties. This composition has the advantage of being less likely to produce black streaks on molded products when exposed to high shear forces during injection molding.
(従来の技術)
スチレン系樹脂等の熱可塑性樹脂にシリコーンオイルを
添加して自己潤滑性を付与する技術は、例えば特開昭6
0−171117号公報や特開昭62−39610号公
報等により公知である。(Prior art) The technology of adding silicone oil to thermoplastic resins such as styrene resins to impart self-lubricating properties is known, for example, from JP-A No. 6
This method is known from Japanese Patent Application Laid-open No. 0-171117, Japanese Patent Application Laid-Open No. 62-39610, and the like.
また、実際この自己潤滑性樹脂組成物は、摺動部材とし
て長らく使用されていたポリアセタールの代替材として
VTRのリールハブ材やOA機器等の摺動部材に多量に
使用されている。Furthermore, in fact, this self-lubricating resin composition is widely used in sliding members such as VTR reel hub materials and office automation equipment as a substitute for polyacetal, which has been used for a long time as sliding members.
(発明が解決しようとする課題)
しかし、この自己潤滑性樹脂組成物には、射出成形時に
樹脂組成物を高剪断力で溶融させて成形すると、「黒条
」とよばれる成形品に黒いスジ状のマークが発生すると
いう欠点がある。この黒条はVTRリールハブ等、無着
色品として使用される用途では重大な成形不良現象の一
つとして扱われ、黒条の発生した成形品は、製品として
使用できなくなるので、製造上大きな問題となる。(Problem to be Solved by the Invention) However, when this self-lubricating resin composition is melted and molded with high shear force during injection molding, black streaks called "black streaks" appear on the molded product. It has the disadvantage of producing marks. These black streaks are treated as a serious molding defect in applications where uncolored products are used, such as VTR reel hubs, and molded products with black streaks can no longer be used as products, resulting in a major manufacturing problem. Become.
この黒条発生の原因は、スチレン系樹脂組成物中のシリ
コーンオイルが樹脂と相溶性が無い為に、樹脂溶融特高
剪断状態に樹脂がさらされると樹脂から分離して、成形
機スクリューとシリンダー内壁との間に生じた微量の金
m¥Aを拾い出す為であろうと考えられる。つまり、シ
リコーンオイルの添加量と、樹脂の剪断状態に起因して
いるので、シリコーンオイルの添加量を減らすか、樹脂
溶融時に高剪断状態にならないように成形機及びスクリ
ュー形状を変更することによって黒条を無くすことは可
能である。The cause of these black streaks is that the silicone oil in the styrene resin composition is not compatible with the resin, so when the resin is exposed to extremely high shear conditions during resin melting, it separates from the resin, causing the screws and cylinders of the molding machine to It is thought that this is to pick up a trace amount of gold m¥A that was generated between the inner wall and the inner wall. In other words, the problem is caused by the amount of silicone oil added and the shear state of the resin, so it is possible to reduce the amount of silicone oil added or change the molding machine and screw shape so that the high shear state does not occur when melting the resin. It is possible to eliminate the clause.
しかし、上記の解決策は実用的ではなく、シリコーンオ
イルの添加量を減らせば、自己潤滑性が得られず、成形
機やスクリューの変更は、高価なものとなってしまうの
で問題点の解決とはならず、安価で済む解決策はこれま
で知られていなかった。However, the above solution is not practical, and reducing the amount of silicone oil added does not provide self-lubricating properties, and changing the molding machine and screw will be expensive, so it is difficult to solve the problem. Until now, no inexpensive solution was known.
(問題点の解決手段)
発明者は、スチレン系樹脂にシリコーンオイルが特定量
添加された自己潤滑性樹脂組成物に、ステアリン酸と炭
素数が1〜10であるアルコールから構成されるステア
リン酸エステルを特定量添加することにより、上記問題
点を解決した黒条の発生しない自己潤滑性スチレン系樹
脂組成物を得て、本発明が完成した。(Means for solving the problem) The inventor added a stearic acid ester composed of stearic acid and an alcohol having 1 to 10 carbon atoms to a self-lubricating resin composition in which a specific amount of silicone oil is added to a styrene resin. By adding a specific amount of , a self-lubricating styrenic resin composition which solves the above problems and does not generate black streaks was obtained, and the present invention was completed.
即ち、本発明は、スチレン系樹脂1. O0重量部に対
してシリコーンオイル045〜10重量部及びステアリ
ン酸と炭素数が1〜10であるアルコールから構成され
るステアリン酸エステル0.1〜3重量部を含有するこ
とを特徴とする自己潤滑性を有するスチレン系樹脂組成
物である。That is, the present invention provides styrenic resin 1. A self-lubricating product characterized by containing 045 to 10 parts by weight of silicone oil and 0.1 to 3 parts by weight of a stearic acid ester consisting of stearic acid and an alcohol having 1 to 10 carbon atoms per 0 parts by weight. It is a styrene-based resin composition with properties.
以1に、本発明についてさらに説明する。The present invention will be further explained below.
本発明に使用するスチレン系樹脂としては、ポリブタジ
ェン等のゴム存在下又は非存在下、スチレンに代表され
る芳香族ビニル化合物を単独又は他の共重合可能な化合
物と重合してなる樹脂である。The styrenic resin used in the present invention is a resin obtained by polymerizing an aromatic vinyl compound represented by styrene alone or with other copolymerizable compounds in the presence or absence of a rubber such as polybutadiene.
ゴムとしては、ポリブタジェン、スチレン−ブタジェン
ゴム、アクリロニトリル−ブタジェンなどのゴム弾性を
をするものが挙げられる。Examples of the rubber include those having rubber elasticity such as polybutadiene, styrene-butadiene rubber, and acrylonitrile-butadiene rubber.
スチレン以ダの芳香族ビニル化合物としてはαメチルス
チレン等のものが挙げられる。Examples of aromatic vinyl compounds other than styrene include α-methylstyrene and the like.
他の共重合可能な化合物としては、アクリロニトリル、
メタリロニトリル、メチルメタアクリレート等のビニル
基を有する非芳香化合物が挙げられる。Other copolymerizable compounds include acrylonitrile,
Examples include non-aromatic compounds having a vinyl group such as metalrylonitrile and methyl methacrylate.
スチレン系樹脂としてより具体的には、ポリスチレン(
ps)、ゴム強化ポリスチレン(Hl−PS) 、アク
リロニトリル−スチレン共重合体(AS)、アクリロニ
トリル−ブタジェン−スチレン共重合体(ABS)、ス
チレン−メチルメタクリレート共重合体(MS)などの
樹脂が挙げられる。More specifically, polystyrene (
ps), rubber-reinforced polystyrene (Hl-PS), acrylonitrile-styrene copolymer (AS), acrylonitrile-butadiene-styrene copolymer (ABS), and styrene-methyl methacrylate copolymer (MS). .
本発明において使用するシリコーンオイルは樹脂に内包
させる添加量は制限されるが、その種類は特に制限は無
く以下の式で示したポリシロキサン結合を有する線状の
重合体で、一般にシリコーンオイルと称される物を使用
する。The silicone oil used in the present invention is limited in the amount added to the resin, but there is no particular restriction on its type, and it is a linear polymer having polysiloxane bonds as shown in the formula below, and is generally called silicone oil. Use what is available.
但し式中のX及びYはアルキル基、フェニル基、ハロア
ルキル基又はへロフェニル基等を示し、nは繰り返し単
位数である。However, in the formula, X and Y represent an alkyl group, a phenyl group, a haloalkyl group, a herophenyl group, etc., and n is the number of repeating units.
シリコーンオイルとしては、安価で入手しやす(、自己
潤滑性付与効果の高いことから前記式のX及びYがメチ
ル基であるポリジメチルシロキサンを用いることが好ま
しい、又、特に規定するものでは無いが、シリコーンオ
イルの粘度としては樹脂への添加を考えた場合、加工性
能から1ooo〜3000Qc s (25℃)、特
に10000〜30QOOc s (25”C)のも
のを使用することが望ましい。As the silicone oil, it is preferable to use polydimethylsiloxane, in which X and Y in the above formula are methyl groups, because it is cheap and easily available (and has a high self-lubricity imparting effect, although it is not particularly specified. The viscosity of the silicone oil is preferably from 1000 to 3000 Qcs (25°C), especially from 10000 to 30Qcs (25''C), considering its processing performance, when considering addition to the resin.
本発明においてシリコーンオイルの添加量はスチレン系
樹脂100重量部に対して0.5〜lO重量部である。In the present invention, the amount of silicone oil added is 0.5 to 10 parts by weight per 100 parts by weight of styrene resin.
なぜならば、0.5重量部未満では樹脂組成物に自己潤
滑性がみられず10重量部を超えると樹脂組成物製造時
の加工性に支障をきたすと共に、成形物の機械的物性が
低下して実用に供さなくなるからである。さらにシリコ
ーンオイルの望ましい添加量は、加工性、自己潤滑性及
び機械的物性の面から樹脂100重量部に対して2〜5
重量部である。This is because if the amount is less than 0.5 parts by weight, the resin composition will not have self-lubricating properties, and if it exceeds 10 parts by weight, the processability during production of the resin composition will be hindered and the mechanical properties of the molded product will deteriorate. This is because it would not be of practical use. Furthermore, the desirable addition amount of silicone oil is 2 to 5 parts by weight per 100 parts by weight of the resin from the viewpoint of processability, self-lubricating property, and mechanical properties.
Parts by weight.
本発明における成形品の黒条発生という問題点の解決策
として添加するステアリン酸エステルは、ステアリン酸
と炭素数が1〜10であるアルコ−ルによって構成され
るエステルであって、その添加量はスチレン系樹脂10
0重量部に対して0.1〜3重量部である。添加量が0
.1重量部未満であれば黒条発生を防止することが出来
ず、3重量部を超えると樹脂組成物の物性を低下させて
しまい実用に供しなくなる。The stearic acid ester added as a solution to the problem of black streaks in molded products in the present invention is an ester composed of stearic acid and an alcohol having 1 to 10 carbon atoms, and the amount added is Styrene resin 10
The amount is 0.1 to 3 parts by weight relative to 0 parts by weight. Added amount is 0
.. If it is less than 1 part by weight, it will not be possible to prevent the formation of black streaks, and if it exceeds 3 parts by weight, the physical properties of the resin composition will deteriorate and it will no longer be of practical use.
エステル体を構成する炭素数1〜10のアルコールの具
体例とし1では、炭素数が1であるメチルアルコール、
炭素数が2であるエチルアルコールなどの低級アルコー
ルから炭素数が10であるデシルアルコールなどの高級
アルコールが挙げられる。さらに上記アルコールの中で
も望ましい種類としては、エステル体として添加しても
物性低下の低いことから、炭素数の少ないアルコールが
好ましく、具体的には炭素数1〜4までのメチルアルコ
ール、エチルアルコール、プロピルアルコール、ブチル
アルコールが特に挙げられる。Specific examples of alcohols having 1 to 10 carbon atoms constituting the ester body include methyl alcohol having 1 carbon number;
Examples include lower alcohols such as ethyl alcohol having 2 carbon atoms and higher alcohols such as decyl alcohol having 10 carbon atoms. Furthermore, among the above alcohols, alcohols with a small number of carbon atoms are preferable because they cause less deterioration of physical properties even when added as an ester, and specifically, methyl alcohol, ethyl alcohol, propyl alcohol with 1 to 4 carbon atoms are preferable. Particular mention may be made of alcohol and butyl alcohol.
一方ステアリン酸以外のアルキルエステルまたは炭素数
がlOを越えるアルコールとのステアリン酸エステルで
は、黒条を解決することが出来な本発明のスチレン系樹
脂組成物を製造する方法は特に制限は無い、具体的に示
すならば、スチレン早樹脂、シリコーンオイル及びステ
アリン酸エステルをヘンシェルミキサー等の混合機によ
り混合した後、車軸や2軸押出機等の混練機で溶融混練
して得る方法、予め加熱液化したステアリン酸エステル
をシリコーンオイルに混合して均一に分散させたものを
車軸や2軸押出機等の混線機でスチレン系樹脂熔融混練
中に添加して得る方法笠がある。On the other hand, when using an alkyl ester other than stearic acid or a stearic acid ester with an alcohol having more than 10 carbon atoms, there are no particular limitations on the method for producing the styrenic resin composition of the present invention that can solve the black streaks. Specifically, styrene early resin, silicone oil, and stearic acid ester are mixed in a mixer such as a Henschel mixer, and then melted and kneaded in a kneading machine such as an axle or twin-screw extruder. There is a method in which stearic acid ester is mixed with silicone oil and uniformly dispersed and added to the process of melting and kneading styrenic resin in a mixer such as an axle or twin-screw extruder.
(実施例)
以下に実施例を挙げて本発明の効果をさらに詳述するが
、本発明はその主旨からはずれないかぎり、これらの実
施例に限定されるものではない。(Examples) The effects of the present invention will be described in more detail with reference to Examples below, but the present invention is not limited to these Examples unless it deviates from the gist thereof.
実施例1.2及び比較例1〜・5
第1表に記載の配合処方で材籾をヘンシェルミキサーで
予備混合した後、同方向2軸押出機を使用してシリンダ
ー温度220℃で溶融混練してベレットを得た。Example 1.2 and Comparative Examples 1 to 5 After premixing paddy wood with the formulation shown in Table 1 using a Henschel mixer, it was melt-kneaded using a co-directional twin-screw extruder at a cylinder temperature of 220°C. and got a beret.
第1表 配合処分(重量部)
’ILxイ七メ1tに1=1−141kjべこa H
l−R−5fiイt+m式プ)ミ9」ヨ1ν10R−2
000ステアリン酸メチル
ステアリン酸デシル
ステアリン酸ブチル
ベヘニン酸ベヘニル
ポリジメチルシロキサン(25°Cにおける粘度125
00 C3)次に得られたベレットを約3オンスの射出
容量を持つスクリュー式射出成形機を使用し成形温度2
20°C1金型温度50゛Cで成形し、引張強度及び対
同質材比摩耗量を評価するための試験片を得た。Table 1 Mixing disposal (parts by weight) 'IL x 1 to 1 ton = 1-141 kj a H
l-R-5fit+m type pu)mi9''yo1ν10R-2
000 Methyl stearate Decyl stearate Butyl behenate Polydimethylsiloxane (viscosity at 25°C 125
00 C3) Next, the obtained pellet was molded at a molding temperature of 2 using a screw injection molding machine with an injection capacity of about 3 ounces.
A test piece was obtained by molding at a mold temperature of 20°C and 50°C to evaluate the tensile strength and wear amount relative to a homogeneous material.
得られた試験片についてASTM D−638に従い
引張試験を行い、そして対同質材比摩耗量の測定は東京
試験機製作所説のビンオンディスク式摩耗試験機を使用
して行った。The obtained test piece was subjected to a tensile test in accordance with ASTM D-638, and the wear amount relative to a homogeneous material was measured using a bottle-on-disk type wear tester manufactured by Tokyo Shikenki Seisakusho.
具体的な比摩耗量の測定方法は以下の通りである。まず
成形しておいたφ120X2mmの円板を下にφ5X3
0mmのビンを上にしてビンに荷重を10kgf掛けて
円板と接触させた。その後ビンを接触させたまま円板を
回転速度500rpm(2rt+/5ec)でビンの総
摩耗距離がlkmになるまで回転させ、この時の摩耗1
(mm’ )を測定した。最終的には、摩耗量を単位
w1mcikgf)、単位距離(I km)あたりの摩
耗体積(man’ )を表す比摩耗量[ms’/(kg
f−km) ]に換算した。A specific method for measuring specific wear amount is as follows. First, place the previously formed φ120x2mm disc on the bottom.
A load of 10 kgf was applied to the bottle with the 0 mm bottle facing upward, and the bottle was brought into contact with the disc. After that, the disk was rotated at a rotational speed of 500 rpm (2rt+/5ec) with the bottle in contact until the total wear distance of the bottle reached 1km, and at this time the wear 1
(mm') was measured. Finally, the unit of wear is w1mcikgf), and the specific wear amount [ms'/(kg
f-km) ].
黒条の評価は、前述の射出成形機を使用して成形温度1
80℃、スクリュー回転数20Orpmで5″xo、5
” xo、125” (2点ゲート)の試験片を成形
して目視による評価を行った。The black streaks were evaluated using the injection molding machine described above at a molding temperature of 1.
80℃, screw rotation speed 20Orpm, 5″xo, 5
"xo, 125" (2-point gate) test pieces were molded and visually evaluated.
具体的には20個の成形品の黒条発生程度を、1個ずつ
目視で見て黒条発生の無い試験片は[○]、薄く黒条が
発生した試験片は[△]、明瞭に黒条の発生した試験片
を〔×〕として判定した。そして20個の成形品中[0
]が15個以上で[×]が無いものをA、[01と[Δ
]を合わせて15個以上のものをB、それ以外の〔×]
が多いものをCとして、その成形品の黒条の発生度を示
した。Specifically, the degree of black streaks in 20 molded products was visually checked one by one. Test pieces with no black streaks were marked [○], and test pieces with thin black streaks were marked [△]. A test piece with black streaks was rated as [x]. And out of 20 molded products [0
] is 15 or more and there is no [×], A, [01 and [Δ
] are 15 or more in total, B, other [×]
The molded product with a large amount of black streaks was designated as C, and the degree of occurrence of black streaks in the molded product was indicated.
引張強度、対同質材比摩耗量及び黒条の評価結果を第2
表に示す。The evaluation results of tensile strength, wear amount relative to homogeneous material, and black streaks were evaluated in the second
Shown in the table.
第2表 評価結果
第2表にまとめた結果より、シリコーンオイルを添加し
−C自己潤滑性を付与したスチレン系樹脂組成物に、ス
テアリン酸と炭素数が1〜10であるアルコールとのエ
ステルを適切!添加すると、射出成形時に樹脂を高剪断
力で熔融させて成形しても黒条の無い成形品を得られる
ことが明らかである。Table 2 Evaluation Results From the results summarized in Table 2, an ester of stearic acid and an alcohol having 1 to 10 carbon atoms was added to a styrenic resin composition to which silicone oil was added to give -C self-lubricating properties. appropriate! It is clear that when added, a molded product without black streaks can be obtained even if the resin is melted and molded with high shear force during injection molding.
(発明の効果)
本発明のスチレン系樹脂組成物は自己潤滑性を有しなが
ら、黒条の無い成形品を得ることができる。(Effects of the Invention) The styrenic resin composition of the present invention has self-lubricating properties and can provide molded products without black streaks.
手続補正書 昭和63年12日7日Procedural amendment 12th and 7th, 1986
Claims (1)
0.5〜10重量部及びステアリン酸と炭素数が1〜1
0であるアルコールから構成されるステアリン酸エステ
ル0.1〜3重量部を含有することを特徴とする自己潤
滑性を有するスチレン系樹脂組成物。0.5 to 10 parts by weight of silicone oil and stearic acid with 1 to 1 carbon number per 100 parts by weight of styrene resin
1. A styrenic resin composition having self-lubricating properties, characterized in that it contains 0.1 to 3 parts by weight of a stearic acid ester composed of alcohol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27630488A JPH06102747B2 (en) | 1988-10-25 | 1988-11-02 | Self-lubricating styrene resin composition |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63-268892 | 1988-10-25 | ||
JP26889288 | 1988-10-25 | ||
JP27630488A JPH06102747B2 (en) | 1988-10-25 | 1988-11-02 | Self-lubricating styrene resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02191650A true JPH02191650A (en) | 1990-07-27 |
JPH06102747B2 JPH06102747B2 (en) | 1994-12-14 |
Family
ID=26548518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27630488A Expired - Fee Related JPH06102747B2 (en) | 1988-10-25 | 1988-11-02 | Self-lubricating styrene resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06102747B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019021546A1 (en) * | 2017-07-28 | 2019-01-31 | テクノUmg株式会社 | Sliding resin composition and body molded therefrom |
-
1988
- 1988-11-02 JP JP27630488A patent/JPH06102747B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019021546A1 (en) * | 2017-07-28 | 2019-01-31 | テクノUmg株式会社 | Sliding resin composition and body molded therefrom |
Also Published As
Publication number | Publication date |
---|---|
JPH06102747B2 (en) | 1994-12-14 |
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