JPH0786166B2 - Polyacetal resin composition - Google Patents
Polyacetal resin compositionInfo
- Publication number
- JPH0786166B2 JPH0786166B2 JP18566190A JP18566190A JPH0786166B2 JP H0786166 B2 JPH0786166 B2 JP H0786166B2 JP 18566190 A JP18566190 A JP 18566190A JP 18566190 A JP18566190 A JP 18566190A JP H0786166 B2 JPH0786166 B2 JP H0786166B2
- Authority
- JP
- Japan
- Prior art keywords
- polyacetal
- weight
- value
- resin 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.)
- Expired - Lifetime
Links
- 229930182556 Polyacetal Natural products 0.000 title claims description 23
- 229920006324 polyoxymethylene Polymers 0.000 title claims description 23
- 239000011342 resin composition Substances 0.000 title claims description 8
- 229920002545 silicone oil Polymers 0.000 claims description 10
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 239000003921 oil Substances 0.000 description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 239000001993 wax Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 5
- 238000005299 abrasion Methods 0.000 description 4
- MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 3
- 230000000669 biting effect Effects 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 3
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 2
- 230000032798 delamination Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920005027 Ultraform® Polymers 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- XWVQUJDBOICHGH-UHFFFAOYSA-N dioctyl nonanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCC(=O)OCCCCCCCC XWVQUJDBOICHGH-UHFFFAOYSA-N 0.000 description 1
- -1 dioctyl pimelate Chemical compound 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 102200082816 rs34868397 Human genes 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明はポリアセタール樹脂組成物に係り、詳しくはス
クリュー食い込み性に優れ、しかも摩擦、摩耗特性の優
れた成形体になるポリアセタール樹脂組成物に関する。TECHNICAL FIELD The present invention relates to a polyacetal resin composition, and more particularly to a polyacetal resin composition which is a molded product having excellent screw biting property and excellent friction and wear characteristics.
[従来技術] 一般にポリアセタールは金属に比較して自己潤滑性に優
れ、低摩擦係数で摩擦、摩耗特性が良く、軽量で駆動時
の騒音が小さいため、軸受、歯車、ローラー、カムガイ
ドレール等の無注油部品として極めて有用である。ナイ
ロン6、66等と比較して平衡吸水率が極めて小さいた
め、寸法安定性が良く、吸水による機械的物性の低下が
非常に小さいので、その用途は多方面にわたっている。[Prior Art] Generally, polyacetal is superior to metal in self-lubricating property, has low friction coefficient, good friction and wear characteristics, is light in weight, and has low noise during driving. It is extremely useful as a non-lubricated component. Its equilibrium water absorption is extremely small compared to nylon 6, 66, etc., so it has good dimensional stability, and its mechanical properties are not significantly degraded by water absorption, so its application is wide-ranging.
しかしながら摺動部品としてみた場合、限界PV値が比較
的低いため、低負荷の用途に限定されている。However, when viewed as sliding parts, the PV limit value is relatively low, so it is limited to low-load applications.
尚、ここでいう限界PV値とは一般に軸受材料が、ある一
定の面圧P(kg/cm2)と周速(m/min)以上になると材
料が融けたり、焼け付いたりする負荷の限界値を示す。
従って、限界PV値が大きい程、摩擦摩耗特性は良好であ
り高負荷に耐えることを意味する。The limit PV value here is generally the limit of the load at which the bearing material melts or burns above a certain surface pressure P (kg / cm 2 ) and peripheral speed (m / min). Indicates a value.
Therefore, the larger the limit PV value is, the better the friction and wear characteristics are, and the higher the load can be endured.
このため、従来からポリアセタールの摩擦、摩耗特性を
改善するために二硫化モリブデン、グラファイト、四フ
ッ化エチレン微粉末、オイル、ワックス等の潤滑剤を添
加することが行なわれている。Therefore, in order to improve the friction and wear characteristics of polyacetal, it has been customary to add a lubricant such as molybdenum disulfide, graphite, fine powder of tetrafluoroethylene, oil or wax.
また、オイル、ワックスの様な成形中に液状である潤滑
剤を添加する場合にはオイル、ワックスを予め活性炭や
ポリノルボルネン等の吸油体に含油させた後、溶融混合
していた。When a liquid lubricant such as oil or wax is added during molding, the oil or wax is impregnated in advance in an oil absorbent such as activated carbon or polynorbornene and then melt mixed.
[発明が解決しようとする課題] しかし、潤滑剤として二硫化モリブデン、グラファイト
を使用すると樹脂の色が黒色に限定されるばかりでな
く、四フッ化エチレン微粉末やオイル、ワックスを使用
した場合に比べて、摩擦、摩耗特性の向上の効果が得ら
れなかった。[Problems to be Solved by the Invention] However, when molybdenum disulfide or graphite is used as a lubricant, not only the color of the resin is limited to black, but also when tetrafluoroethylene fine powder, oil or wax is used. In comparison, the effect of improving the friction and wear characteristics was not obtained.
また、四フッ化エチレン微粉末を使用しても二硫化モリ
ブデン、グラファイトよりも滑剤としての効果はあるも
のの、オイル、ワックス類よりは劣っており、且つ高価
であるという問題点を有していた。一方、オイル、ワッ
クス類を使用すると摩擦摩耗特性の点で優れているが、
スクリュー押出をしようとすると、スクリューの食い込
み性が悪いという問題があった。Further, even if fine powder of tetrafluoroethylene is used, it is more effective as a lubricant than molybdenum disulfide and graphite, but it is inferior to oils and waxes and has a problem that it is expensive. . On the other hand, when oils and waxes are used, it is superior in terms of friction and wear characteristics,
When screw extrusion is attempted, there is a problem that the biteability of the screw is poor.
また、オイル、ワックス類を活性炭やポリノルボルネン
等の吸油体に含油させる方法のうち活性炭を吸油体とし
て使用すれば、樹脂が黒色に限定されてしまい、また活
性炭が摩擦、摩耗特性の点でマイナス因子になってい
た。他方、ポリノルボルネンを吸油体として使用すれ
ば、ポリノルボルネンが主鎖中に二重結合を有している
ため耐熱性に劣り、且つポリノルボルネン系エラストマ
自身が摩擦、摩耗特性の点が活性炭と同様もしくはそれ
以上にマイナス因子となるという問題点があった。In addition, if activated carbon is used as the oil absorber in the method of impregnating oil or waxes into the oil absorber such as activated carbon or polynorbornene, the resin is limited to black, and the activated carbon has negative friction and wear characteristics. It was a factor. On the other hand, when polynorbornene is used as an oil absorber, polynorbornene has a double bond in the main chain and thus is inferior in heat resistance, and the polynorbornene elastomer itself has the same friction and wear characteristics as activated carbon. Or, there was a problem that it became a negative factor.
本発明は上記の課題を解消し、スクリュー食い込み性を
改善し、しかも摩擦、摩耗特性の優れた、また機械的強
度にも優れた成形体になるポリアセタール樹脂組成物を
提供することを目的とするものである。An object of the present invention is to provide a polyacetal resin composition which solves the above-mentioned problems, improves screw biting property, and has excellent friction and wear characteristics, and also has excellent mechanical strength. It is a thing.
[課題を解決するための手段] 即ち、本発明はポリアセタール100重量部にシリコーン
オイルの0.1〜4重量部と一般式が、 H17C8OOC(CH2)nCOOC8H17 (ただし、nは4〜8までの整数)で表される化合物の
0.5〜8重量部を配合したポリアセタール樹脂組成物で
ある。[Means for Solving the Problems] That is, in the present invention, 100 parts by weight of polyacetal and 0.1 to 4 parts by weight of silicone oil are used, and the general formula is H 17 C 8 OOC (CH 2 ) n COOC 8 H 17 (however, n Is an integer of 4 to 8)
It is a polyacetal resin composition containing 0.5 to 8 parts by weight.
尚、本発明のポリアセタール樹脂組成物は、種々の形態
を有するものであり、例えば所定の成分を配合した混合
物を押出機にて溶融混練りして得られたペレットであ
り、また前記ペレットを用いて射出成形機、押出成形機
等にて丸棒、筒状、板状等の所定形状に作成した成形
体、あるいは所定成分を配合した混合物であって、未だ
溶融固化していないものを含む。Incidentally, the polyacetal resin composition of the present invention has various forms, for example, pellets obtained by melt-kneading a mixture containing predetermined components in an extruder, and using the pellets A molded product formed into a predetermined shape such as a round bar, a tubular shape, or a plate shape by an injection molding machine, an extrusion molding machine, or the like, or a mixture containing predetermined components, which is not yet melted and solidified.
本発明で用いるポリアセタールは、ホモポリマーCH2
−On、コポリマーCH2−OnCH2−CH2−O
mのいずれでも良く、数平均分子量20,000〜100,000を
有している。The polyacetal used in the present invention is a homopolymer CH 2
-O n, copolymers CH 2 -O n CH 2 -CH 2 -O
The number average molecular weight is 20,000 to 100,000.
また、ここで用いられるシリコーンオイルは、ジメチル
ポリシロキサンの構造を持ち、粘度が100cSt(センチス
トークス)以上のもので、中でも3000cSt以上のものが
好適である。これらのオイルは、ポリアセタール100重
量部に対して0.1〜4重量部添加されるが、0.1重量部未
満では十分な限界PV値が得られない。また4重量部を越
えると射出成形する場合にはデラミネイションをおこし
たり、スクリューに食い込まなかったりする。ポリアセ
タールにシリコーンオイルを添加すると摩擦摩耗特性の
うち限界PV値の向上に著しい効果があるものの、耐摩耗
性には十分な効果が得られない。Further, the silicone oil used here has a structure of dimethylpolysiloxane and has a viscosity of 100 cSt (centistokes) or more, preferably 3000 cSt or more. These oils are added in an amount of 0.1 to 4 parts by weight with respect to 100 parts by weight of polyacetal, but if the amount is less than 0.1 parts by weight, a sufficient limiting PV value cannot be obtained. Further, if it exceeds 4 parts by weight, when injection molding is performed, delamination may occur or the screw may not bite. Addition of silicone oil to polyacetal has a remarkable effect on improving the limiting PV value in friction and wear characteristics, but does not provide sufficient effect on wear resistance.
一方、本発明で使用するもう一種のオイル、即ち一般式
を、 H17C8OOC(CH2)nCOOC8H17 (但し、nは4〜8までの整数)で表される化合物でジ
オクチルアジペート、ジオクチルピメレート、ジオクチ
ルスペレート、ジオクチルアゼレート、ジオクチルセバ
ケートの5つが挙げられ、限界PV値の向上より、むしろ
耐摩耗性に著しい効果があることが認められた。On the other hand, another oil used in the present invention, that is, a compound represented by the general formula: H 17 C 8 OOC (CH 2 ) n COOC 8 H 17 (where n is an integer of 4 to 8) is dioctyl. Adipate, dioctyl pimelate, dioctyl sperate, dioctyl azelate, and dioctyl sebacate were mentioned, and it was recognized that the abrasion resistance was more effective than the improvement of the critical PV value.
更に、上記化合物は、 H17C8OOC(CH2)nCOOC8H17 という構造の中で中間のメチレン基が4〜8個存在す
る。このメチレン基を4〜8個もつ化合物とポリアセタ
ール樹脂との相溶性が適度であるため、機械的強度の低
下が比較的小さく、且つ摺動面に適度ににじみでてくる
ので耐摩耗性に寄与する。一方、上記化合物においてn
が3以下となるとメチレン基が少なく、ポリアセタール
との相溶性が良いため、ポリアセタール樹脂の可塑剤と
なり、機械的強度が大巾に低下する。Further, the above compound has 4 to 8 intermediate methylene groups in the structure of H 17 C 8 OOC (CH 2 ) n COOC 8 H 17 . Since the compatibility between the compound having 4 to 8 methylene groups and the polyacetal resin is moderate, the decrease in mechanical strength is relatively small, and the sliding surface moderately bleeds, contributing to wear resistance. To do. On the other hand, in the above compound, n
When it is 3 or less, the number of methylene groups is small and the compatibility with the polyacetal is good, so that it becomes a plasticizer for the polyacetal resin, and the mechanical strength is greatly reduced.
また、相溶性が良いことでポリアセタール内へ取り込ま
れてしまい摺動面へのにじみ出し量が少ないので耐摩耗
性への寄与が相対的に小さい。つまり本発明ではシリコ
ーンオイルでは十分な効果を得にくい耐摩耗性について
一般式を H17C8OOC(CH2)nCOOC8H17 (但し、nは4〜8までの整数)で表される化合物で補
完するものであり、0.5〜8重量部をポリアセタールに
添加するのが好ましい。0.5重量部未満では十分な耐摩
耗性が得られず、8重量部を越えるとスクリュー食い込
み性が悪くなる場合がある。また、ポリアセタールに添
加する上記オイルの総重量が10重量部を越えると機械的
特性が低下し、実用上問題となる。Further, since the compatibility is good, it is taken into the polyacetal and the amount of bleeding to the sliding surface is small, so that the contribution to the wear resistance is relatively small. That is, in the present invention, the general formula for abrasion resistance, which is difficult to obtain a sufficient effect with silicone oil, is represented by H 17 C 8 OOC (CH 2 ) n COOC 8 H 17 (where n is an integer from 4 to 8). It is complementary to the compound, and it is preferable to add 0.5 to 8 parts by weight to the polyacetal. If it is less than 0.5 parts by weight, sufficient abrasion resistance cannot be obtained, and if it exceeds 8 parts by weight, the screw biting property may deteriorate. Further, if the total weight of the above-mentioned oil added to the polyacetal exceeds 10 parts by weight, the mechanical properties will deteriorate, which is a practical problem.
本発明組成物は、上記ポリアセタール樹脂、シリコーン
オイルとを通常の押出機で混練することによって得るこ
とができる。この押出成形、射出成形での押出温度は19
0〜210℃の範囲が好ましい。190℃より低い温度で押出
すと、樹脂が硬くスクリューに食い込みにくい。また、
210℃より高い温度で押出すと、樹脂が焼けたり分解し
易くなるので適当とは言えない。The composition of the present invention can be obtained by kneading the above polyacetal resin and silicone oil with an ordinary extruder. The extrusion temperature in this extrusion molding and injection molding is 19
The range of 0 to 210 ° C is preferable. If extruded at a temperature lower than 190 ° C, the resin will be hard and will not easily penetrate into the screw. Also,
Extrusion at a temperature higher than 210 ° C is not suitable because the resin tends to burn or decompose.
尚、本発明は上記添加剤以外に目的に応じた充填剤、補
強材、各種添加剤や着色剤を用いて実施することも可能
である。The present invention can be carried out by using a filler, a reinforcing material, various additives and a coloring agent according to the purpose other than the above additives.
以下、本発明を実施例により更に詳述するが、これらの
実施例のみに限定するものではない。Hereinafter, the present invention will be described in more detail by way of examples, but the present invention is not limited to these examples.
[実施例] 実施例および比較例に使用した原材料を一括して示すと
次の通りである。即ち、 ウルトラフォルムN2320(BASF社製) シリコーンオイル 10万cSt(東レ・ダウユーニン
グ・シリコーン社製) ジオクチルセバケート(DOS)(三建化工(株)
製) ジオクチルアジペート(DOA)(大八化学(株)
製) [実施例1〜5] 上記各原材料〜を表1の実施例に示す通り配合し、
2軸押出機(池貝鉄工社製:PCM−45)に供給し溶融混練
してペレットを得た。このペレットを用いて射出成形機
で試験片を作成し、得られた成形体の限界PV値とスラス
ト摩耗値と曲げ強さを測定した。結果を表1に示す。[Examples] Raw materials used in Examples and Comparative Examples are collectively shown below. Ultraform N2320 (manufactured by BASF) Silicone oil 100,000 cSt (manufactured by Toray Downing Silicone) Dioctyl sebacate (DOS) (Sanken Kako Co., Ltd.)
Dioctyl adipate (DOA) (Dahachi Chemical Co., Ltd.)
Manufacture) [Examples 1 to 5] The above raw materials were blended as shown in Examples of Table 1,
The mixture was supplied to a twin-screw extruder (PCM-45 manufactured by Ikegai Iron Works Co., Ltd.) and melt-kneaded to obtain pellets. Using the pellets, test pieces were prepared with an injection molding machine, and the limit PV value, thrust wear value, and bending strength of the obtained molded body were measured. The results are shown in Table 1.
尚、限界PV値の求め方は松原式スラスト試験より測定
し、試験片はφ50×3t、相手材S45C円筒状(φ25.6×φ
20)で10分毎に面圧を10kg/cm2上げてゆき、その面圧を
保持できない時の圧力Pと速度Vの積を限界PV値とし
た。The method of obtaining the limit PV value was measured by the Matsubara thrust test, the test piece was φ50 × 3t, the mating material S45C cylindrical shape (φ25.6 × φ
In 20), the surface pressure was increased by 10 kg / cm 2 every 10 minutes, and the product of the pressure P and the speed V when the surface pressure could not be maintained was defined as the limit PV value.
また、スラスト摩耗量は上と同じ試験機、試験片を使用
し、面圧20kg/cm2、速度15m/min、24時間試験し、試験
前後の重量差をもってスラスト摩耗量とした。The thrust wear amount was tested by using the same tester and test piece as above, with a surface pressure of 20 kg / cm 2 and a speed of 15 m / min for 24 hours, and the weight difference before and after the test was used as the thrust wear amount.
[比較例1〜6] 前記諸原材料〜を表1の比較例1〜6の配合とした
以外は実施例1〜4と全く同様の操作を行なって試験片
を作製し、実施例と同様の試験を行なった。結果を表1
に示す。[Comparative Examples 1 to 6] Specimens were prepared in the same manner as in Examples 1 to 4 except that the raw materials 1 to 3 were blended as in Comparative Examples 1 to 6 in Table 1 to prepare test pieces. The test was conducted. The results are shown in Table 1.
Shown in.
表1に示す配合と測定結果からわかるように実施例にお
いては限界PV値がある程度以上の数値を示しており、か
つスラスト摩耗値についても小さな数値が得られてい
る。そして、比較例1より明らかにポリアセタールだけ
より両方の数値とも優れており、比較例2よりシリコー
ンオイルのみを配合したものが限界PV値では実施例と同
じ程度の数値を示しているがスラスト摩耗値では劣って
いる。比較例3、6はシリコーンオイルやDOSを過剰に
配合すると成形はできてもデラミネーションをおこした
り、ペレットがスクリューに食い込まず成形できないこ
とを示しており、比較例4、5ではシリコーンオイルを
配合していないと限界PV値が高くならないことがわか
る。 As can be seen from the composition and the measurement results shown in Table 1, in the examples, the limit PV value shows a certain value or more, and the thrust wear value also has a small value. Then, both values are clearly superior to only polyacetal from Comparative Example 1, and the one containing only silicone oil from Comparative Example 2 shows the same limit PV value as that of the Example, but the thrust wear value. Is inferior. Comparative Examples 3 and 6 show that when silicone oil or DOS is excessively blended, molding is possible but delamination occurs, or pellets do not bite into the screw and cannot be molded. In Comparative Examples 4 and 5, silicone oil is blended. It can be seen that the marginal PV value does not increase without it.
[効果] 以上の様に本発明によれば、シリコーンオイルと一般式
を、 H17C8OOC(CH2)nCOOC8H17 (但しnは4〜8までの整数)で表される化合物の両者
を配合することにより、限界PV値と耐摩耗性両方の物性
が優れ、更に機械的強度にも優れたポリアセタール樹脂
組成物を得ることができる。[Effect] As described above, according to the present invention, a compound represented by H 17 C 8 OOC (CH 2 ) n COOC 8 H 17 (where n is an integer from 4 to 8) is represented by the general formula. By blending both of the above, it is possible to obtain a polyacetal resin composition which is excellent in both physical properties such as a limiting PV value and abrasion resistance and further excellent in mechanical strength.
Claims (1)
イルの0.1〜4重量部と一般式が、 H17C8OOC(CH2)nCOOC8H17 (但しnは4〜8までの整数)で表される化合物の0.5
〜8重量部を配合したことを特徴とするポリアセタール
樹脂組成物。Claims: 1. 100 parts by weight of polyacetal and 0.1 to 4 parts by weight of silicone oil, and the general formula is H 17 C 8 OOC (CH 2 ) n COOC 8 H 17 (where n is an integer from 4 to 8). 0.5 of the compound
A polyacetal resin composition characterized by containing 8 to 8 parts by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18566190A JPH0786166B2 (en) | 1990-07-13 | 1990-07-13 | Polyacetal resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18566190A JPH0786166B2 (en) | 1990-07-13 | 1990-07-13 | Polyacetal resin composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0477546A JPH0477546A (en) | 1992-03-11 |
| JPH0786166B2 true JPH0786166B2 (en) | 1995-09-20 |
Family
ID=16174659
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18566190A Expired - Lifetime JPH0786166B2 (en) | 1990-07-13 | 1990-07-13 | Polyacetal resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0786166B2 (en) |
-
1990
- 1990-07-13 JP JP18566190A patent/JPH0786166B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0477546A (en) | 1992-03-11 |
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