JPH0362741B2 - - Google Patents

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Publication number
JPH0362741B2
JPH0362741B2 JP56116380A JP11638081A JPH0362741B2 JP H0362741 B2 JPH0362741 B2 JP H0362741B2 JP 56116380 A JP56116380 A JP 56116380A JP 11638081 A JP11638081 A JP 11638081A JP H0362741 B2 JPH0362741 B2 JP H0362741B2
Authority
JP
Japan
Prior art keywords
nylon
weight
friction
tracking resistance
present
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
Application number
JP56116380A
Other languages
Japanese (ja)
Other versions
JPS5819355A (en
Inventor
Hironobu Kawasaki
Masayuki Oohata
Junichi Nakabashi
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP11638081A priority Critical patent/JPS5819355A/en
Publication of JPS5819355A publication Critical patent/JPS5819355A/en
Publication of JPH0362741B2 publication Critical patent/JPH0362741B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は、摩擦摩耗特性、耐トラツキング性、
機械物性、耐熱性のすぐれたスライドスイツチ用
材料に関する。 従来、電気分野の摺動部材、特にスライドスイ
ツチ等にはフエノール樹脂がそのその優れた電気
的性質、機械的性質のために多用されてきたが、
この樹脂は耐トラツキング性に劣るという重大な
欠点を有している。 このため、本発明者らは、このような欠点を改
良した材料として、ポリアミド系材料を考えた。
しかし、非補強ポリアミドは機械的強度、耐熱性
が充分でなかつた。また、これを改良した材料と
して補強ポリアミドを考えたが、これらを用いた
時、スライドスイツチ用材料として必須の摩擦摩
耗特性、耐トラツキング性に問題のある場合の多
いことがわかつた。 本発明者らはこれら欠点を解消した材料を得べ
く鋭意検討した結果、ある種の無機充填剤とナイ
ロン66との組成物が、摩擦摩耗特性、耐トラツキ
ング性、機械的強度、耐熱性に優れていることを
見出し、本発明に到達した。 即ち本発明は、アルミニウムの硅酸塩および/
またはマグネシウムの硅酸塩である無機質充填剤
10〜60重量%とナイロン66 40〜90重量%とから
なるスライドスイツチ用材料に関する。 一般にポリアミドに用いられる無機質充填剤に
は数多くの化合物がある。 これらの無機質化合物を表示するのに、一つは
該化合物成分の特徴的な元素、また一つはこれら
元素の存在形態を示す方法がある。 特徴的な元素として、マグネシウム、アルミニ
ウム、ケイ素、カリウム、カルシウム、チタン等
が挙げられる。 元素の存在形態として、酸化物、炭酸塩、硅酸
塩、硫酸塩等がある。 本発明者等はこれらの数多くの化合物について
鋭意検討した結果、これらのうち、アルミニウム
の硅酸塩とマグネシウムの硅酸塩だけがスライド
スイツチ用材料成分として適性のあることを見出
した。 即ち、アルミニウムまたはマグネシウムの硅酸
塩とナイロン66の組成物は、スライドスイツチ用
材料として必要な摩擦摩耗特性、耐トラツキング
性、機械的強度及び耐熱性のいずれをも満足する
ことを見出した。 一方、その他の無機質充填剤は、いずれもスラ
イドスイツチ用材料成分としての適性に欠けるこ
とがことがわかつた。例えば、けい素の酸化物、
カルシウムの硅酸塩は摩擦摩耗特性に劣り(ポリ
アミドの補強剤として常用されるガラス繊維も同
様)、カルシウムの炭酸塩は耐熱性が不十分であ
り、チタン酸カリウムは耐トラツキング性が不良
である。 本発明でいうマグネシウムの硅酸塩には、タル
ク、セピオライト、エンスタタイト等があるが特
にタルクが好ましい。 本発明でいうアルミニウムの硅酸塩には、カオ
リン、マイカ、シラマイト、ピロフイルライト等
があるが特にカオリン、マイカが好ましい。 これらの無機質充填剤の添加量は、10〜60重量
%である。好ましくは15〜50重量%、更に好まし
くは20〜40重量%である。10重量%未満の場合、
機械的性質(引張強度、圧縮強度等)、耐熱性が
充分でない。60重量%を越える場合、機械的性質
及び耐熱性のそれ以上の向上はあまり期待できな
いうえ、この無機質充填剤とナイロン66との溶融
混練時の混練性及び該ナイロン66組成物を成形す
る際の成形性が著しく悪くなる。 これら無機質充填剤のナイロン66への配合方法
は、常用の方法が利用でき、例えば、無機質充填
剤とナイロン66造粒物とをドライブレンドしこれ
を溶融混練する方法、無機質充填剤とナイロン66
造粒物とをドライブレンドしそのまま成形に供す
る方法等がある。また、無機質充填剤をナイロン
66に添加する際、カツプリング剤を用いること、
無機質充填剤をよく分散させることは摩擦摩耗特
性、機械的性質、耐熱性に効果的である。 本発明でいうナイロン66とは、ナイロン66の特
性を損なわない範囲内で共重合したポリアミド共
重合体も含まれる。 本発明の材料は、ナイロン66に、前述したアル
ミニウムの硅酸塩および/またはマグネシウムの
硅酸塩である無機質充填剤に加えて一般に摺動特
性改良剤として知られるカーボンフイバー、ポリ
テトラフルオロエチレン粉末等を含有していても
よく、また、摩擦摩耗特性に悪影響を及ぼさない
範囲において、ガラス繊維、ウオラストナイト、
シリカ等を添加してもよい。その他に、銅化合
物、アルカリ金属のハロゲン化塩、りん化合物等
の熱安定剤、有機ハロゲン化物、アンチモン化合
物等の難燃剤、有機アミド化合物、有機エステル
化合物等の離型剤、高級脂肪酸、その金属塩等の
滑剤、カーボンブラツク、顔料、染料等の着色剤
等を含有してもよい。 本発明の材料は、特に自動車向のスライドスイ
ツチでその効果を最大に発揮する。 本発明のスライドスイツチ用材料は、摩擦摩耗
特性、耐トラツキング性に優れ、機械的性質、耐
熱性も充分に高いものである。 以下、実施例により本発明を更に詳しく説明す
る。 なお、実施例中の摩擦摩耗特性、耐トラツキン
グ性、引張強度、圧縮強度、熱変形温度の測定は
次のようにして行つた。 摩擦摩耗特性:下記の条件で試験片と相手材
(銅)とを摺動させ、摺動前後の相手材の重量
差を測定した。 試験機:東洋ボールドウイン社製摩擦摩耗試験機
EFM−−B型 (試験片と相手材の接触状態を図面に示す。) 測定条件:相手材;銅 面圧;10Kg/cm2; 摺動線速度;5cm/sec 摺動時間;4Hr 耐トラツキング性:DIN−KA法に従つた。 引張強度:ASTM−D−638に従つた。 圧縮強度:ASTM−D−695に従つた。 熱変形温度:ASTM−D−648に従つた。 実施例 1 ナイロン66(旭化成工業(株)製レオナ#1300)80
重量%にタルク((株)龍森社製CRS6002)20重量
%を混合し、石中鉄工(株)社製70mmφ単軸押出機に
て溶融混練造粒を行い。ナイロン66組成物ペレツ
トを得た。これを射出成形機にて成形し、摩擦摩
耗特性、耐トラツキング性、引張強度、圧縮強
度、熱変形温度を測定した。測定結果を表1に示
す。 実施例 2〜4 実施例1と同様の実験をタルク40重量%(実施
例2)、カオリン(林化成(株)製ASP−200)20重
量%(実施例3)、マイカ(白石工業(株)製325M)
20重量%(実施例4)について行つた。但し、実
施例2〜4についてはフイラーにシラン系カツプ
リング剤処理を施した。その結果を表1に示す。 比較例 1 フエノール樹脂について、耐トラツキング性試
験を行つた。その結果を表1に示す。 比較例 2 ナイロン66 67重量%とガラス繊維33重量%と
を混練押出しし、これを成形し摩擦摩耗特性及び
耐トラツキング性、引張強度、圧縮強度、熱変形
温度を測定した。その結果を表1に示す。 比較例 3 ナイロン66 80重量%とチタン酸カリウム(大
塚化学薬品(株)製テイスモタイプD)20重量%とを
溶融混練造粒し、これを成形し、耐トラツキング
性を測定した。その結果を表1に示す。 比較例 4 ナイロン66について引張強度、圧縮強度、熱変
形温度を測定した。その結果を表1に示す。 表1の結果から、フエノール樹脂は耐トラツキ
ング性に劣ること、ナイロン66にガラス繊維を配
合したものは、耐トラツキング性は改善されてい
るものの摩擦摩耗特性に劣ること、またナイロン
66にチタン酸カリウムを配合したものでは耐トラ
ツキング性が充分でないことがわかる。一方本発
明の材料は、摩擦摩耗特性、耐トラツキング性、
機械的性質、耐熱性のいずれがすぐれていること
がわかる。 【表】
DETAILED DESCRIPTION OF THE INVENTION The present invention provides friction and wear characteristics, tracking resistance,
This invention relates to materials for slide switches with excellent mechanical properties and heat resistance. Conventionally, phenolic resin has been widely used for sliding parts in the electrical field, especially slide switches, etc. due to its excellent electrical and mechanical properties.
This resin has a serious drawback of poor tracking resistance. For this reason, the present inventors considered a polyamide-based material as a material that improves upon such drawbacks.
However, non-reinforced polyamides did not have sufficient mechanical strength and heat resistance. We also considered reinforcing polyamide as an improved material, but found that when these were used, there were often problems with the friction and wear characteristics and tracking resistance, which are essential for slide switch materials. The inventors of the present invention conducted intensive studies to obtain a material that overcomes these drawbacks, and found that a composition of a certain type of inorganic filler and nylon 66 has excellent friction and wear characteristics, tracking resistance, mechanical strength, and heat resistance. The present invention was achieved based on the discovery that That is, the present invention provides an aluminum silicate and/or
Or an inorganic filler that is magnesium silicate.
The present invention relates to a material for a slide switch comprising 10 to 60% by weight of nylon 66 and 40 to 90% by weight of nylon 66. There are many compounds as inorganic fillers commonly used in polyamides. In order to display these inorganic compounds, there are two methods: one method is to show the characteristic elements of the compound components, and the other method is to show the existing forms of these elements. Characteristic elements include magnesium, aluminum, silicon, potassium, calcium, titanium, etc. The existing forms of elements include oxides, carbonates, silicates, and sulfates. The inventors of the present invention have intensively studied a large number of these compounds, and have found that among them, only aluminum silicate and magnesium silicate are suitable as material components for slide switches. That is, it has been found that a composition of aluminum or magnesium silicate and nylon 66 satisfies all of the friction and wear characteristics, tracking resistance, mechanical strength, and heat resistance required as a material for a slide switch. On the other hand, it has been found that all other inorganic fillers lack suitability as material components for slide switches. For example, silicon oxide,
Calcium silicates have poor friction and wear properties (as do glass fibers commonly used as reinforcing agents in polyamides), calcium carbonates have insufficient heat resistance, and potassium titanate has poor tracking resistance. . The magnesium silicate used in the present invention includes talc, sepiolite, enstatite, etc., and talc is particularly preferred. Examples of the aluminum silicate used in the present invention include kaolin, mica, sillamite, and pyrofilite, with kaolin and mica being particularly preferred. The amount of these inorganic fillers added is 10 to 60% by weight. Preferably it is 15 to 50% by weight, more preferably 20 to 40% by weight. If it is less than 10% by weight,
Mechanical properties (tensile strength, compressive strength, etc.) and heat resistance are insufficient. If it exceeds 60% by weight, further improvements in mechanical properties and heat resistance cannot be expected, and the kneading properties during melt-kneading of this inorganic filler and nylon 66 and when molding the nylon 66 composition are Moldability deteriorates significantly. Conventional methods can be used to blend these inorganic fillers into nylon 66, such as dry blending the inorganic filler and nylon 66 granules and melt-kneading them;
There is a method of dry blending the granulated material and directly molding it. In addition, inorganic filler is added to nylon.
When adding to 66, use a coupling agent,
Good dispersion of inorganic fillers is effective for improving friction and wear properties, mechanical properties, and heat resistance. The nylon 66 used in the present invention also includes polyamide copolymers copolymerized within a range that does not impair the properties of nylon 66. The material of the present invention includes nylon 66, carbon fiber, polytetrafluoroethylene, which is generally known as a sliding property improver, in addition to the above-mentioned inorganic filler which is aluminum silicate and/or magnesium silicate. It may contain powder, etc., and may contain glass fiber, wollastonite, etc. as long as it does not adversely affect the friction and wear characteristics.
Silica etc. may be added. In addition, heat stabilizers such as copper compounds, halide salts of alkali metals, phosphorus compounds, flame retardants such as organic halides and antimony compounds, mold release agents such as organic amide compounds and organic ester compounds, higher fatty acids, and their metals. It may also contain lubricants such as salts, colorants such as carbon black, pigments, dyes, etc. The material of the present invention exhibits its effects to the maximum especially in slide switches for automobiles. The slide switch material of the present invention has excellent friction and wear characteristics and tracking resistance, and has sufficiently high mechanical properties and heat resistance. Hereinafter, the present invention will be explained in more detail with reference to Examples. In addition, measurements of friction and wear characteristics, tracking resistance, tensile strength, compressive strength, and heat distortion temperature in Examples were performed as follows. Friction and wear characteristics: A test piece and a mating material (copper) were slid under the following conditions, and the difference in weight between the mating material before and after sliding was measured. Testing machine: Toyo Baldwin Friction and Wear Testing Machine
EFM--Type B (The contact state between the test piece and the mating material is shown in the drawing.) Measurement conditions: Comparing material: Copper Surface pressure: 10Kg/cm 2 ; Sliding linear speed: 5cm/sec Sliding time: 4Hr Tracking resistance Gender: According to DIN-KA method. Tensile strength: According to ASTM-D-638. Compressive strength: According to ASTM-D-695. Heat distortion temperature: According to ASTM-D-648. Example 1 Nylon 66 (Leona #1300 manufactured by Asahi Kasei Corporation) 80
The mixture was mixed with 20% by weight of talc (CRS6002 manufactured by Ryumori Co., Ltd.) and melted, kneaded, and granulated using a 70 mmφ single-screw extruder manufactured by Ishinaka Tekko Co., Ltd. Nylon 66 composition pellets were obtained. This was molded using an injection molding machine, and its friction and wear characteristics, tracking resistance, tensile strength, compressive strength, and heat distortion temperature were measured. The measurement results are shown in Table 1. Examples 2 to 4 An experiment similar to Example 1 was conducted using 40% by weight of talc (Example 2), 20% by weight of kaolin (ASP-200 manufactured by Hayashi Kasei Co., Ltd.) (Example 3), and mica (Shiraishi Kogyo Co., Ltd.). )325M)
20% by weight (Example 4). However, in Examples 2 to 4, the filler was treated with a silane coupling agent. The results are shown in Table 1. Comparative Example 1 A tracking resistance test was conducted on a phenolic resin. The results are shown in Table 1. Comparative Example 2 67% by weight of nylon 66 and 33% by weight of glass fiber were kneaded and extruded, molded, and measured for friction and wear characteristics, tracking resistance, tensile strength, compressive strength, and heat distortion temperature. The results are shown in Table 1. Comparative Example 3 80% by weight of nylon 66 and 20% by weight of potassium titanate (Teismo Type D manufactured by Otsuka Chemical Co., Ltd.) were melt-kneaded and granulated, molded and the tracking resistance was measured. The results are shown in Table 1. Comparative Example 4 The tensile strength, compressive strength, and heat distortion temperature of nylon 66 were measured. The results are shown in Table 1. From the results in Table 1, it can be seen that phenolic resin has poor tracking resistance, that nylon 66 mixed with glass fiber has improved tracking resistance but has poor friction and wear properties, and that nylon 66 has poor tracking resistance.
It can be seen that the tracking resistance of 66 mixed with potassium titanate is not sufficient. On the other hand, the material of the present invention has friction and wear properties, tracking resistance,
It can be seen that both mechanical properties and heat resistance are excellent. 【table】

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

図面は、摩擦摩耗特性測定の際の試験片と相手
材との接触状態を示す正面図である。図中、1は
試験片(固定する)、2は相手材(銅)、3は試験
片1と相手材2との摺動面を示す。
The drawing is a front view showing the state of contact between a test piece and a mating material when measuring friction and wear characteristics. In the figure, 1 indicates a test piece (to be fixed), 2 indicates a mating material (copper), and 3 indicates a sliding surface between the test specimen 1 and the mating material 2.

Claims (1)

【特許請求の範囲】 1 アルミニウムの硅酸塩および/またはマグネ
シウムの硅酸塩である無機質充填剤10〜60重量%
とナイロン66 40〜90重量%とからなるスライド
スイツチ用材料。 2 アルミニウムの硅酸塩がカオリン、マイカ、
マグネシウムの硅酸塩がタルクである特許請求の
範囲第1項記載のスライドスイツチ用材料。
[Claims] 1. 10 to 60% by weight of an inorganic filler that is an aluminum silicate and/or a magnesium silicate.
A slide switch material consisting of nylon 66 and 40 to 90% by weight. 2 Aluminum silicate is kaolin, mica,
The material for a slide switch according to claim 1, wherein the magnesium silicate is talc.
JP11638081A 1981-07-27 1981-07-27 Polyamide sliding material Granted JPS5819355A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11638081A JPS5819355A (en) 1981-07-27 1981-07-27 Polyamide sliding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11638081A JPS5819355A (en) 1981-07-27 1981-07-27 Polyamide sliding material

Publications (2)

Publication Number Publication Date
JPS5819355A JPS5819355A (en) 1983-02-04
JPH0362741B2 true JPH0362741B2 (en) 1991-09-26

Family

ID=14685563

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11638081A Granted JPS5819355A (en) 1981-07-27 1981-07-27 Polyamide sliding material

Country Status (1)

Country Link
JP (1) JPS5819355A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS617353A (en) * 1984-06-21 1986-01-14 Oiles Ind Co Ltd Aromatic polyamide resin sliding member and manufacture thereof
JP2015219965A (en) * 2014-05-14 2015-12-07 佐鳥エス・テック株式会社 Trigger switch
WO2020202833A1 (en) * 2019-03-29 2020-10-08 日本電産株式会社 Small gear and gear unit
WO2020202835A1 (en) * 2019-03-29 2020-10-08 日本電産株式会社 Small-sized component

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS517056A (en) * 1974-07-08 1976-01-21 Teijin Ltd NAIRON JUSHI SEIBUTSU
JPS5171349A (en) * 1974-12-18 1976-06-21 Toyo Boseki HORIAMIDOSOSEIBUTSU
JPS51127217A (en) * 1975-02-17 1976-11-05 Teijin Ltd Pulp particles
JPS5845465B2 (en) * 1975-08-20 1983-10-11 旭化成株式会社 Polyamide materials
JPS52105958A (en) * 1976-03-02 1977-09-06 Teijin Ltd Polyamide composition
IT1083439B (en) * 1976-08-26 1985-05-21 Allied Chem MOLDING COMPOSITIONS BASED ON NAILON LOADED WITH MINERAL SUBSTANCES LOW PERMANENT DEFORMATION
JPS6037829B2 (en) * 1977-07-08 1985-08-28 日産化学工業株式会社 Flame retardant polyamide composition

Also Published As

Publication number Publication date
JPS5819355A (en) 1983-02-04

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