JPS63212518A - Manufacture of sliding part - Google Patents

Manufacture of sliding part

Info

Publication number
JPS63212518A
JPS63212518A JP26231386A JP26231386A JPS63212518A JP S63212518 A JPS63212518 A JP S63212518A JP 26231386 A JP26231386 A JP 26231386A JP 26231386 A JP26231386 A JP 26231386A JP S63212518 A JPS63212518 A JP S63212518A
Authority
JP
Japan
Prior art keywords
shaft
bearing surface
lactam
omega
clearance
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
JP26231386A
Other languages
Japanese (ja)
Other versions
JPH0618743B2 (en
Inventor
Hiroshi Isekawa
伊勢川 洋
Tatsuya Kato
加藤 辰也
Takahiro Iwase
隆広 岩瀬
Nobuo Kobayashi
信夫 小林
Hirotake Sugimoto
杉本 裕剛
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.)
Mitsubishi Kasei Polytec Co
Toyota Motor Corp
Original Assignee
Mitsubishi Monsanto Chemical Co
Toyota Motor Corp
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 Mitsubishi Monsanto Chemical Co, Toyota Motor Corp filed Critical Mitsubishi Monsanto Chemical Co
Priority to JP61262313A priority Critical patent/JPH0618743B2/en
Publication of JPS63212518A publication Critical patent/JPS63212518A/en
Publication of JPH0618743B2 publication Critical patent/JPH0618743B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To prevent a line from a solution A tank bottom to a rotary valve and also a clearance between a shaft and a bearing surface from getting clogged by forming resin linings prepared through the process of heating omega-lactam molten substance solution A containing polymerization catalysts at the given temperature on the bearing surface. CONSTITUTION:With a shaft fitted into a bearing face and supported revolvably or reciprocatively, omega-lactam molten substance solution A containing polymerization catalysts for alkaline metal or alkali earth metal compound and omega-lactam molten substance solution B containing polymerization co-catalysts are injected into a clearance between said shaft and bearing surface and polymerically cured to form resin linings on the bearing surface and manufacture a sliding part for sliding the shaft on said linings. In that case, omega-lactam molten substance solution A containing polymerization catalysts is prepared through the process of being heated at the temperature of approximately 110 deg.C. By said process, the line is almost prevented from getting blocked because of the floatings in solution A, and the clogging at clearances between the shaft of the sliding part and the bearing surface is remarkably prevented from occurring and a good resin lining may be formed.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、摺動部品の製造方法に関するものであり、よ
り詳しくはポリアミド系反応射出成形法により樹脂ライ
ニングした摺動部品の製造方法に関するものである。
Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a method for manufacturing sliding parts, and more particularly to a method for manufacturing resin-lined sliding parts using a polyamide reaction injection molding method. It is.

(従来の技術) ポリアミド系反応射出成形においては、重合触媒を含む
ω−ラクタム溶融状物CAM)と重合助触媒を含むω−
ラクタムの溶融状物(B液)とを、同時に金型に注入ま
えは射出し、金型内で反応させ成形品とされる。従来、
上記A液はω−ラクタムと重合触媒とをそれぞれ別々に
計量し、あらかじめ設定した温度、時間条件で溶解し、
その後冷却固化させて調製し、B液と反応上行なうとき
に再溶解していた。
(Prior art) In polyamide-based reaction injection molding, an ω-lactam melt (CAM) containing a polymerization catalyst and an ω-lactam melt containing a polymerization co-catalyst are used.
A molten lactam (liquid B) is simultaneously injected into a mold and reacted in the mold to form a molded product. Conventionally,
The above-mentioned liquid A is made by weighing the ω-lactam and the polymerization catalyst separately, and dissolving them under preset temperature and time conditions.
It was then prepared by cooling and solidifying, and was redissolved when reacting with liquid B.

(発明が解決しようとする問題点) 上記の従来法によりポリアミド系反応射出成形した樹脂
によりライニングされた摺動部品を製造する場合には、
以下n#に説明するポリアミド系反応射出成形機におい
て、特にA液のタンク底からロータリーバルブに至る管
路で管内が閉塞されて吐出不能をきたすばかりでなく、
摺動部品の軸を軸受に嵌合して回転または往復自在に支
持し喪状態で軸と軸受面とのクリアランスに注入すると
き、A[が該クリアランスに均−lこゆきわたらないと
いう欠点があった。
(Problems to be Solved by the Invention) When manufacturing sliding parts lined with polyamide-based reaction injection molded resin by the above-mentioned conventional method,
In the polyamide reaction injection molding machine described in n# below, the pipe from the bottom of the A liquid tank to the rotary valve is not only blocked, but also becomes incapable of discharging.
When the shaft of a sliding part is fitted into a bearing and supported so that it can rotate or reciprocate freely, and when it is injected into the clearance between the shaft and the bearing surface, there is a drawback that A does not evenly spread over the clearance. Ta.

第4図に反応射出成形機のシステム概念因を示す。タン
ク11.22.24に各々A液21.B液23.洗浄液
25を入れ、各タンク内め温度を温調体20により約9
0℃に保ち、タンク11内はインペラ12により撹拌す
る。次に吐出に際しては、プランジャポンプ13及びI
 S’が作動し、ロータリーバルブ14が図示した状態
においてタンク11及び22より各々A液21及びB液
23がプランジャポンプ室15及び15′に入る。次に
ロータリーバルブ14を反#tillJりの方向へ90
”回転し、プランジャポンプ15及び13′か作動し、
AM21及びB液23は管路17を通り、スタティック
ミキサー18に至り、ここでAg21及びB液2sが混
合されて、吐出口19より、軸と軸受面とのクリアラン
ス(図示せず)に射出される。
Figure 4 shows the system concept of the reaction injection molding machine. A liquid 21. into tanks 11, 22, and 24 respectively. B liquid 23. Pour in the cleaning liquid 25 and adjust the temperature inside each tank to about 9
The temperature inside the tank 11 is maintained at 0° C., and the inside of the tank 11 is stirred by an impeller 12. Next, when discharging, the plunger pump 13 and I
S' is activated, and with the rotary valve 14 in the state shown, liquid A 21 and liquid B 23 enter the plunger pump chambers 15 and 15' from the tanks 11 and 22, respectively. Next, move the rotary valve 14 in the opposite direction by 90 degrees.
``rotates, plunger pumps 15 and 13' operate,
AM21 and B liquid 23 pass through a pipe line 17 and reach a static mixer 18, where Ag21 and B liquid 2s are mixed and injected from a discharge port 19 into the clearance between the shaft and the bearing surface (not shown). Ru.

以上の反り射出成形機に3いて、従来法に従って摺動部
品を製造すると、′#1路16が約2遍間で閉塞してし
まい、吐出不能に至るし、管路16が閉塞しない場合で
も、混合液を軸と軸受面とのクリアランスに充分に注入
できないという問題が起こる。特にA液吐出量が1回5
%l以下と少量である場合には、上記の現象の一万また
は両方が急速に発生し、生産性を著しく低下させている
If a sliding part is manufactured using the above-mentioned warp injection molding machine according to the conventional method, the #1 passage 16 will be blocked approximately twice, resulting in the inability to eject, and even if the pipe line 16 is not blocked, , a problem arises in that the mixed liquid cannot be sufficiently injected into the clearance between the shaft and the bearing surface. In particular, the amount of A liquid discharged per time is 5.
When the amount is as small as %l or less, one or both of the above phenomena occur rapidly, significantly reducing productivity.

上記のような現象が多発するのは、A液中にω−ラクタ
ムと混入されている重合触媒そのもの、この分解生成物
またはオリゴマー等が遊離し、ω−ラクタム溶液中に浮
遊して存在しており、その結果タンク11内ではインペ
ラ12で常時攪拌されていても、管路16内では静止静
態が断続的に存在し、前記した浮遊物が管路壁に徐々に
沈降付着したり、軸と軸受面とのクリアランスに詰まっ
たりする九めである。管路壁への付着の場合は、これが
進行すると、付着した物質が配管外からの移動熱に対し
、断熱作用を及ぼし、さらに管路温度の低下にき丸し、
管路壁への浮遊物の付着を一層助長することになる。
The reason why the above phenomenon frequently occurs is that the polymerization catalyst itself mixed with ω-lactam in liquid A, its decomposition products or oligomers, etc. are liberated and exist suspended in the ω-lactam solution. As a result, even though the tank 11 is constantly agitated by the impeller 12, a stationary state exists intermittently in the pipe line 16, causing the above-mentioned floating substances to gradually settle and adhere to the pipe wall, or to become attached to the shaft. The ninth problem is that it gets stuck in the clearance with the bearing surface. In the case of adhesion to the pipe wall, as this progresses, the adhered substance acts as an insulator against the heat transferred from outside the pipe, further reducing the pipe temperature.
This further promotes the adhesion of floating substances to the pipe walls.

本発明は、上記のような問題点を解決する九めのもので
あり、その目的とするところは、ポリアミド系反応射出
成形樹脂によってライニングされた摺動部品を製造する
場合に、A液タンク底からロータリーバルブに至る管路
の詰まりを防止し、かつ軸と軸受面とのクリアランスの
詰まりを防止する方法を提供することである。
The present invention is the ninth to solve the above-mentioned problems, and its purpose is to prevent the bottom of the liquid A tank from producing sliding parts lined with polyamide-based reaction injection molded resin. It is an object of the present invention to provide a method for preventing clogging of a pipe line leading from a rotary valve to a rotary valve, and also preventing clogging of a clearance between a shaft and a bearing surface.

(問題点を解決するための手段) 本発明の摺動部品の製造方法は、 mt軸軸受嵌合して回転または往復動自在に支持した状
態で、この軸と軸受面とのクリアランスに、アルカリ金
属またはアルカリ土類金属化合物の重合触媒を含むω−
ラクタム溶融状物と重合助触媒を含むω−ラクタム溶融
状物とを注入し重合硬化させて、樹脂ライニングを前記
軸受面に形成し、曲記軸が前記樹脂ライニング上を摺動
するようにした摺動部品を製造するにあたり、前記重合
触媒を含むω−ラクタム溶融状物を110℃付近の温度
で加熱する工程を経て調製することを特徴とする。
(Means for Solving the Problems) In the method of manufacturing a sliding component of the present invention, an alkali is added to the clearance between the shaft and the bearing surface in a state where the mt shaft bearing is fitted and supported so as to be rotatable or reciprocating. ω- containing a polymerization catalyst of metal or alkaline earth metal compound
A lactam melt and an omega-lactam melt containing a polymerization promoter were injected and polymerized and cured to form a resin lining on the bearing surface, so that the curved shaft slid on the resin lining. In producing the sliding part, the sliding part is characterized in that it is prepared through a step of heating an omega-lactam melt containing the polymerization catalyst at a temperature of around 110C.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

本発明においてω−ラクタムは、例えばr−。In the present invention, the ω-lactam is, for example, r-.

ブチロラクタム、δ−バレロラクタム、ε−カプロラク
タム、ω−エナントラクタム、ω−カプリルラクタム、
ω−ウンデカノラクタム、ω−ラウリルラクタムなどで
ある。これらは単独Φ でも、二種類以上の混合物であって良い。
Butyrolactam, δ-valerolactam, ε-caprolactam, ω-enantholactam, ω-capryllactam,
These include ω-undecanolactam and ω-lauryllactam. These Φ may be used alone or as a mixture of two or more types.

上記ω−ラクタムに溶解される1合触媒は、ω−ラクタ
ムの陰イオン重合に従来から使用されているアルカリ金
属、アルカリ土類金属及びそれらの化合物である。具体
的には、アルカリ金属、アルカリ土類金属、これらの水
素化物、アルキル化合物、アリール化合物、史には上記
金属または金属化合物とω−ラクタムとの反応生成物、
例えばω−ラクタムのナトリウム塩、カリウム塩、マグ
ネシウムハライド塩などである。
The single catalyst dissolved in the ω-lactam is an alkali metal, an alkaline earth metal, or a compound thereof, which has been conventionally used for anionic polymerization of ω-lactam. Specifically, alkali metals, alkaline earth metals, hydrides thereof, alkyl compounds, aryl compounds, and in particular, reaction products of the above metals or metal compounds with ω-lactams,
Examples include sodium salt, potassium salt, magnesium halide salt, etc. of ω-lactam.

重合触媒の使用量は、ω−ラクタムに対してα01ない
し20モル%が好ましい。cL01モル%未満の場合は
、B液と反応させたときの重合速度が遅く、さらに微量
の水分の影4を受けて重合しない場合もあり、工業的利
用価値が低い。
The amount of the polymerization catalyst used is preferably α01 to 20% by mole based on the ω-lactam. If cL0 is less than 1 mol %, the polymerization rate when reacted with liquid B is slow, and furthermore, polymerization may not occur due to the shadow 4 of a trace amount of water, and the value of industrial use is low.

また20モル%を超える場合は、最終的に祷られる反応
射出成形品の耐候性を低下させる。このため非常に速い
重合速度を必要とする場合以外は、非経済的である。
Moreover, when it exceeds 20 mol%, the weather resistance of the final reaction injection molded product is reduced. Therefore, it is uneconomical unless a very high polymerization rate is required.

Afiは、上記重合触媒をω−ラクタム′m#a秋物に
混合後、110℃付近例えば90℃ないし130℃の温
度に昇温し、この温度で2時間ないし30分間維持し溶
解する工程を経て祷られるが、該工程は本発明の特筆す
べき1点である。前記した様にA液中にω−ラクタムと
混入されている重合触媒そのもの、この分解生成物また
はオリゴマー等が遊離した浮遊物が、反応射出成形機に
おける管路閉塞または軸と軸受面とのクリアランスの詰
まりの原因となっていた。本発明では、A液の溶$を1
10℃付近、特jc90℃ないいS0℃の範囲に昇温し
、この温度で2時間ないし30分間維持して行なったこ
とにより、上記した浮遊物はω−ラクタム溶融物中に良
好に溶解している。この範囲で維持する時間は、低温側
はど長くし、高温側はど短くするのが良い。このため、
浮遊物の析出が少量となり、管路閉塞が大幅に遅延し、
軸と軸受面とのクリアランスの詰まりも著しく減少する
Afi is prepared by mixing the polymerization catalyst with the ω-lactam'm#a autumn product, raising the temperature to around 110°C, for example, 90°C to 130°C, and maintaining this temperature for 2 to 30 minutes to dissolve it. However, this step is one of the noteworthy points of the present invention. As mentioned above, the polymerization catalyst itself mixed with omega-lactam in liquid A, its decomposition products, or floating substances such as oligomers may cause blockage of pipes or clearance between the shaft and bearing surface in the reaction injection molding machine. This was causing the blockage. In the present invention, the solution of liquid A is 1
By raising the temperature to around 10°C, particularly in the range of 90°C to 0°C, and maintaining this temperature for 2 hours to 30 minutes, the above-mentioned suspended matter was well dissolved in the ω-lactam melt. ing. It is best to keep the temperature within this range longer on the low temperature side and shorter on the high temperature side. For this reason,
A small amount of suspended matter is deposited, and pipe blockage is significantly delayed.
Clogging of the clearance between the shaft and the bearing surface is also significantly reduced.

本発明のB液の14#!に用いられる重合助触媒は、ω
−ラクタムを陰イオン1合法によって重合する際に従来
から使用されている化合物が、全て使用可能である。そ
の具体例としては、例えば、トルエンジイソシアネート
、4.4’−ジフェニルメタンジイソシアネート、ヘキ
サメチレンジイソシアネート、ポリメチレンポリフェニ
ルポリイソシアネート、カルボジイミドで変性されたジ
イソシアネート等のイソシアネート類、ヘキサメチレン
−1,6−ビスカルバミドカプロラクタム、N、N’−
ジフェニル−p−フェニレンビスカルバミドカプロラク
タム、N、N’−ジフェニル−p−7エニレンビスカル
パミドピロリド等のカルバミドラクタム類、テレフタル
酸クロリド、アジピン酸クロリド、セバシン酸クロリド
等の酸ハライド類、アジポイルビスカプロラクタム、ア
ジポイルビスピロリドン、テレフタロイルビスカプロラ
クタム、テレフタロイルビスピロリドン、イソフタロイ
ルビスカプロラクタム等のポリアシルラクタム類、また
は式「式中、人はハロゲン原子tXわずか、またはンを
表わす)であり、aは1,2または3のfflであり、
bは2またはそれ以上の壷畝であり、Rsはアルキル基
、アルアルキル基、アルキルオキシ基、アリールオキシ
基、ハロゲン基またはアルアルキルオキシ基を表わし、
烏は炭化水素基およびエーテル結合を有する炭化水素か
ら選択される2価以上の基を表わし、2は(1)最低分
子量約2000を有するポリエーテル、(2)最低分子
量約2000を有するポリエーテルセグメント金含有す
るポリエステルセグメント、または(3)最低分子量1
000を有する炭化水素を表わす。]で表わされる化合
物からなる群より選択される酸ハライド′1能性物質ま
たはラクタム官能性物質である。
14# of B liquid of the present invention! The polymerization promoter used for ω
- All compounds conventionally used in polymerizing lactams by the anion-one method can be used. Specific examples thereof include isocyanates such as toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, hexamethylene diisocyanate, polymethylene polyphenyl polyisocyanate, diisocyanate modified with carbodiimide, and hexamethylene-1,6-biscarbamide. Caprolactam, N, N'-
Carbamide lactams such as diphenyl-p-phenylenebiscarbamide caprolactam, N,N'-diphenyl-p-7enylenebiscarpamide pyrrolide, acid halides such as terephthalic acid chloride, adipic acid chloride, sebacic acid chloride, adipic acid chloride, etc. Polyacyl lactams such as polybiscaprolactam, adipoylbispyrrolidone, terephthaloylbiscaprolactam, terephthaloylbispyrrolidone, isophthaloylbiscaprolactam, or the formula ``in the formula ``, where ``human'' represents a halogen atom, ), a is ffl of 1, 2 or 3,
b is two or more pot ridges, Rs represents an alkyl group, an aralkyl group, an alkyloxy group, an aryloxy group, a halogen group or an aralkyloxy group,
Karasu represents a divalent or higher group selected from a hydrocarbon group and a hydrocarbon having an ether bond, and 2 represents (1) a polyether having a minimum molecular weight of about 2000, (2) a polyether segment having a minimum molecular weight of about 2000. gold-containing polyester segment, or (3) minimum molecular weight 1
000 represents a hydrocarbon. is an acid halide monofunctional substance or a lactam functional substance selected from the group consisting of compounds represented by:

本発明は、上記のA液及びB液を、軸を軸受に嵌合して
回転または往復動自在に支持し次状態で、この軸と軸受
面とのクリアランスに反応射出成形機等により注入し1
合硬化させて、樹脂ライニングを前記軸受面に形成し、
前記軸が前記樹脂ライニング上を摺動するようにした摺
動部凸金製造する。
In the present invention, the above-mentioned liquids A and B are injected into the clearance between the shaft and the bearing surface using a reaction injection molding machine or the like, after a shaft is fitted into a bearing and supported so as to be rotatable or reciprocating. 1
forming a resin lining on the bearing surface by combining and curing;
A sliding part convex metal is manufactured so that the shaft slides on the resin lining.

(作用) 本発明は、ポリアミド系反応射出成形材料によってライ
ニングされた摺動部品を製造する礪ポリアミド系反応射
出成形においてA液タンク底の管謁閉塞を遅延させ、そ
して材料の注入される軸と軸受面とのクリアランスの詰
まりを大幅に減少させる。
(Function) The present invention delays pipe blockage at the bottom of the liquid A tank in polyamide reaction injection molding for manufacturing sliding parts lined with polyamide reaction injection molding material, and the shaft where the material is injected. Significantly reduces clogging of the clearance with the bearing surface.

(実施例) 次に本発明を実施例に基づいて、さらに詳細に説明する
が、本発明はこれに限定されない。
(Examples) Next, the present invention will be described in more detail based on Examples, but the present invention is not limited thereto.

実施例1 第1図および第2図において、1はアウタースプライン
の軸受、2は軸受1に嵌合し往411Ih自在に支持さ
れたインナースプラインの軸を示し、また3は軸受1の
軸受0k14上にポリアミド糸反応射出成形によって形
成された樹脂ライニング、5及び6は、6出し用センタ
ーである。
Embodiment 1 In FIGS. 1 and 2, 1 indicates the outer spline bearing, 2 indicates the shaft of the inner spline that fits into the bearing 1 and is supported freely in the forward direction, and 3 indicates the shaft on the bearing 0k14 of the bearing 1. The resin lining, 5 and 6, is formed by reaction injection molding of polyamide thread, and is the center for 6 exits.

この5!施例の摺動部品は、まず軸受1の軸受面4に離
型剤を、軸2衣山にはブライマーを塗布し、次にこの軸
受1と輔2を140℃に予備加熱してA液及びB液の注
入にそなえた。
This 5! For the sliding parts of this example, first, a mold release agent is applied to the bearing surface 4 of the bearing 1, and a brimer is applied to the coating surface of the shaft 2. Next, the bearing 1 and the bearing 2 are preheated to 140°C and treated with A liquid and Prepared for injection of B solution.

C−カプロラクタム94.5重量部とブロモマグネシウ
ムカプロラクタム5.5重量部とを混合後110℃に加
熱し1時間この温度付近に保持し、90℃以下に降温し
て冷却固化する工程ヲ経てB14gしたA液と、ε−カ
プロラクタム55.5重量部と次式(17 (但し、式中2は分子量約6000のエチレンオキサイ
ドとプロピレンオキサイドのブロック共重合体を表わす
。) で表わされる重合助触媒44.5重量sとよりなるB液
をvI4製した。これらAtL及びB液を第4図に示す
反応射出成形機のタンク11にA液21を、タンク22
にB液23を入れる。これらタンクは温調体20により
90℃に保たれている。
After mixing 94.5 parts by weight of C-caprolactam and 5.5 parts by weight of bromomagnesium caprolactam, the mixture was heated to 110°C, kept around this temperature for 1 hour, cooled to below 90°C, and solidified by cooling to obtain 14g of B. Liquid A, 55.5 parts by weight of ε-caprolactam, and a polymerization cocatalyst represented by the following formula (17 (where 2 in the formula represents a block copolymer of ethylene oxide and propylene oxide having a molecular weight of about 6000) 44. B liquid consisting of 5 weight s was prepared vI4.These AtL and B liquid were placed in the tank 11 of the reaction injection molding machine shown in FIG.
Add liquid B 23 to. These tanks are maintained at 90° C. by a temperature controller 20.

次にA液21及びB液23が重量比で1:1になるよう
にプランジャポンプ15及び15′を作動じ、両液をス
タティックミキサー18に導き混合し、この混合物を吐
出口19より前記した軸受1内に適量注ぎ、次いで@2
を軸受1に嵌合することにより軸2と軸受面4とのクリ
アランスに厚さtが約o、22闘に混合物を均一にゆき
わたらせ、140℃で5分間保持した。
Next, the plunger pumps 15 and 15' are operated so that the weight ratio of liquid A 21 and liquid B 23 is 1:1, and both liquids are introduced into the static mixer 18 and mixed, and this mixture is passed through the discharge port 19 as described above. Pour an appropriate amount into bearing 1, then @2
was fitted into the bearing 1, so that the mixture was uniformly spread over the clearance between the shaft 2 and the bearing surface 4 with a thickness t of about 22 mm, and the mixture was held at 140° C. for 5 minutes.

得られた摺動部品は、@2と軸受14とのクリアランス
の全面にわたり樹脂ライニング5が形成され、軸2か全
くがたつかなかった。
In the obtained sliding part, the resin lining 5 was formed over the entire clearance between @2 and the bearing 14, and the shaft 2 did not shake at all.

さらに上記の組成からなるA液及びB液を用いて、反応
射出成形機の連続便用によるタンク11の底からロータ
リーバルブ14に至る管路16が閉塞し、吐出不能に至
るまでの期間は4ケ月だった。
Furthermore, using liquids A and B having the above compositions, the period of time until the pipe line 16 from the bottom of the tank 11 to the rotary valve 14 for continuous use of the reaction injection molding machine is blocked and discharging becomes impossible is 4. It was a month.

比較例I A液としてε−カプロラクタム? 4.5 重it 8
(1トブロモマグネシウム力プロラクタム5.5重量部
とを混合しただけのもの’を112用した他は、実施例
1と同様の手順で摺IIeJ部品を形成した。
Comparative Example I ε-caprolactam as liquid A? 4.5 heavy it 8
A Suri IIeJ part was formed in the same manner as in Example 1, except that 112 was prepared by mixing 1 tobromomagnesium and 5.5 parts by weight of prolactam.

僧られた摺動S品は、軸と軸受面のクリアランスには詰
まりが生じ、該クリアランスの全面には樹脂ライニング
が形成されず、しかも軸ががたつくものだった。
In the sliding S product, which had been modified, the clearance between the shaft and the bearing surface was clogged, the resin lining was not formed on the entire surface of the clearance, and the shaft rattled.

さらにこの場合の反応射出成形機の管路の閉塞により吐
出不能に至るまでの期間は2週間だった。
Furthermore, in this case, it took two weeks until the reaction injection molding machine became unable to eject due to blockage of the pipe line.

実施例2 第5図は、他の摺動S品であり、軸受7とこれに嵌合し
回転自在に支持される軸8と、軸受7の軸受面10上に
実施例1で用いたと同種のA液及びBgとの混合物によ
る実施例1と同様の手順で成形した樹脂ライニング9(
厚さ平均a15am)からなる。
Embodiment 2 FIG. 5 shows another sliding S product, including a bearing 7, a shaft 8 fitted therein and rotatably supported, and a bearing surface 10 of the bearing 7 of the same type as used in Embodiment 1. Resin lining 9 (
The average thickness is 15 am).

この摺動部品は、軸8と軸受面10のクリアランスの全
面にわたり樹脂ライニング9が形成され、@8はがたつ
きがなく、円滑な回転運動が可能だった。
In this sliding part, a resin lining 9 was formed over the entire clearance between the shaft 8 and the bearing surface 10, and @8 had no rattling and was capable of smooth rotational movement.

(発明の効果) 本発明の摺wb部分の製造方法によると、A液の浮遊物
に由来する雪路の閉塞が住じ−く、摺動部品の軸と軸受
面とのクリアランスの詰まりが著しく抑えられ、艮好な
樹脂ライニングが形成される。これらのことから、本発
明は摺動部品の生産性を同上させ、その産業上の利用価
値は極めて大である。
(Effects of the Invention) According to the method of manufacturing the sliding wb portion of the present invention, the snowy road is not blocked due to the suspended matter of liquid A, and the clearance between the shaft of the sliding part and the bearing surface is significantly clogged. A beautiful resin lining is formed. For these reasons, the present invention improves the productivity of sliding parts, and its industrial utility value is extremely large.

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

第1図は、本発明の一夾施例の摺m部品を示す断面図、 第2図は、第1図の平面図、 第3図は、本発明の他の実施例の摺#IJ部品を示す断
面図、 第4図は、反応射出成形機のシステム概念図である。 図中、 1.7・・・軸受       2.8・・・輔3.9
・・・a4脂ライニング  4.10・・・軸受面特許
出願人 三菱センサント化成体式会社第1図 23図 牙4図
FIG. 1 is a cross-sectional view showing a sliding part according to one embodiment of the present invention, FIG. 2 is a plan view of FIG. 1, and FIG. 3 is a sliding #IJ component according to another embodiment of the present invention. FIG. 4 is a conceptual system diagram of a reaction injection molding machine. In the diagram, 1.7... Bearing 2.8... 3.9
... A4 fat lining 4.10 ... Bearing surface patent applicant Mitsubishi Sensanto Kasei Shiki Co., Ltd. Fig. 1 Fig. 23 Fig. 4

Claims (1)

【特許請求の範囲】[Claims] 軸を軸受に嵌合して回転または往復動自在に支持した状
態で、この軸と軸受面とのクリアランスに、アルカリ金
属またはアルカリ土類金属化合物の重合触媒を含むω−
ラクタム溶融状物と重合助触媒を含むω−ラクタム溶融
状物とを注入し重合硬化させて、樹脂ライニングを前記
軸受面に形成し、前記軸が前記樹脂ライニング上を摺動
するようにした摺動部品を製造するにあたり、前記重合
触媒を含むω−ラクタム溶融状物を110℃付近の温度
で加熱する工程を経て調製することを特徴とする摺動部
品の製造方法。
When the shaft is fitted into a bearing and supported so that it can rotate or reciprocate, the clearance between the shaft and the bearing surface contains an ω-containing polymerization catalyst of an alkali metal or alkaline earth metal compound.
A lactam melt and an omega-lactam melt containing a polymerization promoter are injected and polymerized and cured to form a resin lining on the bearing surface, and the shaft slides on the resin lining. 1. A method for producing a sliding part, which comprises the step of heating a molten omega-lactam containing the polymerization catalyst at a temperature of around 110°C.
JP61262313A 1986-11-04 1986-11-04 Manufacturing method of sliding parts Expired - Lifetime JPH0618743B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61262313A JPH0618743B2 (en) 1986-11-04 1986-11-04 Manufacturing method of sliding parts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61262313A JPH0618743B2 (en) 1986-11-04 1986-11-04 Manufacturing method of sliding parts

Publications (2)

Publication Number Publication Date
JPS63212518A true JPS63212518A (en) 1988-09-05
JPH0618743B2 JPH0618743B2 (en) 1994-03-16

Family

ID=17374043

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61262313A Expired - Lifetime JPH0618743B2 (en) 1986-11-04 1986-11-04 Manufacturing method of sliding parts

Country Status (1)

Country Link
JP (1) JPH0618743B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2230306A (en) * 1989-04-10 1990-10-17 Mitsubishi Monsanto Chem Producing a sliding coupling by a monomer casting method
US8052328B2 (en) * 2005-09-27 2011-11-08 Ntn Corporation Bearing device with sliding bearing

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61214A (en) * 1984-03-22 1986-01-06 スタミカ−ボン・ベスロ−テン・ベンノ−トシヤツプ Reaction injection formation and formed matter
JPS634911A (en) * 1986-06-26 1988-01-09 Mazda Motor Corp Reaction injection molding device for reinforced nylon molded form
JPS6357207A (en) * 1986-08-29 1988-03-11 Toyota Motor Corp Method of wash purging mixing part and its equipment in reaction injection molding machine

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61214A (en) * 1984-03-22 1986-01-06 スタミカ−ボン・ベスロ−テン・ベンノ−トシヤツプ Reaction injection formation and formed matter
JPS634911A (en) * 1986-06-26 1988-01-09 Mazda Motor Corp Reaction injection molding device for reinforced nylon molded form
JPS6357207A (en) * 1986-08-29 1988-03-11 Toyota Motor Corp Method of wash purging mixing part and its equipment in reaction injection molding machine

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2230306A (en) * 1989-04-10 1990-10-17 Mitsubishi Monsanto Chem Producing a sliding coupling by a monomer casting method
US5114521A (en) * 1989-04-10 1992-05-19 Mitsubishi Monsanto Chemical Company Method for producing a sliding coupling by a monomer casting method
GB2230306B (en) * 1989-04-10 1993-06-30 Mitsubishi Monsanto Chem A method of producing a sliding coupling by a monomer casting method
US8052328B2 (en) * 2005-09-27 2011-11-08 Ntn Corporation Bearing device with sliding bearing

Also Published As

Publication number Publication date
JPH0618743B2 (en) 1994-03-16

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