JPH04351543A - Manufacture of double-layered bearing material made of polyacetal resin composition - Google Patents

Manufacture of double-layered bearing material made of polyacetal resin composition

Info

Publication number
JPH04351543A
JPH04351543A JP3025536A JP2553691A JPH04351543A JP H04351543 A JPH04351543 A JP H04351543A JP 3025536 A JP3025536 A JP 3025536A JP 2553691 A JP2553691 A JP 2553691A JP H04351543 A JPH04351543 A JP H04351543A
Authority
JP
Japan
Prior art keywords
polyacetal resin
base material
resin composition
sintered
sintered base
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.)
Pending
Application number
JP3025536A
Other languages
Japanese (ja)
Inventor
Masao Nakajima
正雄 中島
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.)
NDC Co Ltd
Nippon Dia Clevite Co Ltd
Original Assignee
NDC Co Ltd
Nippon Dia Clevite 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 NDC Co Ltd, Nippon Dia Clevite Co Ltd filed Critical NDC Co Ltd
Priority to JP3025536A priority Critical patent/JPH04351543A/en
Publication of JPH04351543A publication Critical patent/JPH04351543A/en
Pending legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/02Parts of sliding-contact bearings
    • F16C33/04Brasses; Bushes; Linings
    • F16C33/20Sliding surface consisting mainly of plastics
    • F16C33/201Composition of the plastic
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C2208/00Plastics; Synthetic resins, e.g. rubbers
    • F16C2208/20Thermoplastic resins
    • F16C2208/66Acetals, e.g. polyoxymethylene [POM]

Landscapes

  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Sliding-Contact Bearings (AREA)
  • Laminated Bodies (AREA)

Abstract

PURPOSE:To improve adhesiveness by coating a sintered base material consisting of a rear metal and a sintered alloy layer on the rear metal with a polyacetal resin compsn. with a particle diameter of 295mum or smaller, passing through the polyacetal resin compsn. of the sintered base material between upper and lower roils under a heated and melted condition and pushing it into the sintered base material. CONSTITUTION:A sintered base material consisting of a rear metal 1 and a sintered alloy layer 2 on the rear metal 1 is coated with a polyacetal resin compsn. with a particle diameter of 295mum or smaller. Then, the polyacetal resin compsn. with which the sintered base material is coated is melted by heating at 170-200 deg.C and 18 pressed into the sintered base material by passing through it between upper and lower rolls under this condition to make it into a double layer to obtain a required double-layered bearing material made of the polyacetal resin compsn.

Description

【発明の詳細な説明】[Detailed description of the invention]

【0001】0001

【産業上の利用分野】本発明は鋼裏金と焼結合金層なら
びにポリアセタ−ル樹脂系組成物層から成る密着性が良
好な複層軸受の製造方法に係り、特にポリアセタ−ル樹
脂を微粉末とし、これに固体潤滑剤等を加えて組成物と
成し、この組成物を焼結基材の空洞部に満遍なく含浸さ
せることができるポリアセタ−ル樹脂系組成物複層軸受
材の製造方法に係る。
[Industrial Application Field] The present invention relates to a method for manufacturing a multilayer bearing with good adhesion consisting of a steel back metal, a sintered alloy layer, and a polyacetal resin composition layer. A method for manufacturing a polyacetal resin composition multi-layer bearing material, in which a solid lubricant etc. are added to this to form a composition, and this composition is evenly impregnated into the cavities of a sintered base material. Related.

【0002】0002

【従来の技術】ポリアセタ−ル樹脂は機械的特性・耐熱
性・耐久性がハイレベルでバランスし、かつ高い結晶性
と化学的安定性を有し自己潤滑性に優れていることから
軸受材として多用されている。軸受材としては二種類に
大別される。一つは射出成形法等で製作されるポリアセ
タ−ル樹脂単品の成形軸受材であり、もう一つは例えば
英国特許第1091710号に記載されているインデン
ト型(油溜り)のポリアセタ−ル樹脂の複層軸受材であ
る。この複層軸受材の製造方法は溶融ブレンドにより所
定厚のポリアセタ−ル樹脂系組成物のシ−トを作り、次
いで、このシ−トを焼結基材へ積層し、この積層体を所
定寸法・パタ−ンを有するインデント加工ロ−ルに通し
てインデント加工をするといういわゆるシ−ト法が技術
の要点となっている。
[Prior Art] Polyacetal resin is used as a bearing material because it has a high level of balance in mechanical properties, heat resistance, and durability, and also has high crystallinity, chemical stability, and excellent self-lubricating properties. It is widely used. Bearing materials are roughly divided into two types. One is a single molded bearing material made of polyacetal resin manufactured by injection molding, and the other is an indented (oil sump) polyacetal resin bearing material as described in British Patent No. 1,091,710. It is a multilayer bearing material. The manufacturing method for this multilayer bearing material is to create a sheet of a polyacetal resin composition with a predetermined thickness by melt blending, then laminate this sheet onto a sintered base material, and form this laminate into a predetermined size. - The key point of the technology is the so-called sheet method, in which the material is passed through a patterned indentation roll for indentation.

【0003】ところで、ポリアセタ−ル樹脂系組成物シ
−トを焼結基材上に積層する複層化においては、焼結層
が緻密すなわち空孔率が小さい場合や合金が複雑な形状
の場合に樹脂が空洞部に十分充填されないこと、また、
この時、空気が焼結基材と樹脂層の界面に残り、製品と
して使用すると樹脂層のふくれやはがれといった不具合
を引起すことがある。また、シ−ト化は押出成形法を採
っており、初期設備投資やランニングコストの負担も無
視できないという問題があった。
[0003] By the way, in multi-layering in which polyacetal resin composition sheets are laminated on a sintered base material, when the sintered layer is dense, that is, the porosity is small, or when the alloy has a complicated shape, The resin may not be sufficiently filled into the cavity, and
At this time, air remains at the interface between the sintered base material and the resin layer, which may cause problems such as blistering or peeling of the resin layer when used as a product. In addition, the extrusion molding method is used to form sheets, and there is a problem in that the burden of initial equipment investment and running costs cannot be ignored.

【0004】0004

【発明が解決しようとする課題】本発明は上記問題を解
決することを目的とし、具体的には、従来例のシ−ト法
の問題点に着目してなされたもので、ポリアセタ−ル樹
脂系組成物と焼結基材との密着性が良好でふくれやはが
れがなく、しかも、ポリアセタ−ル樹脂系組成物のシ−
ト化する装置を特に設けることなく、ポリアセタ−ル樹
脂系組成物の複層軸受材を得ることができるポリアセタ
−ル樹脂系組成物複層軸受材の製造方法を提案すること
を目的とする。
SUMMARY OF THE INVENTION The present invention aims to solve the above-mentioned problems, and specifically focuses on the problems of the conventional sheet method. The adhesiveness between the polyacetal resin composition and the sintered base material is good, and there is no blistering or peeling.
It is an object of the present invention to propose a method for manufacturing a multilayer bearing material made of a polyacetal resin composition, which can obtain a multilayer bearing material made of a polyacetal resin composition without particularly providing a device for converting the polyacetal resin composition into a composite material.

【0005】[0005]

【課題を解決するための手段】すなわち、本発明は裏金
とこの裏金上に焼結合金層とから成る焼結基材上に粒径
が295μm以下のポリアセタ−ル樹脂系組成物をコ−
ティングし、次いで、このコ−ティングされた焼結基材
のポリアセタ−ル樹脂系組成物を加熱溶融状態で上下ロ
−ル間を通し焼結基材に圧入して複層化することを特徴
とする。
[Means for Solving the Problems] That is, the present invention coats a polyacetal resin composition having a particle size of 295 μm or less on a sintered base material consisting of a backing metal and a sintered metal layer on the backing metal.
Then, the polyacetal resin composition of the coated sintered base material is heated and molten and passed between upper and lower rolls and press-fitted into the sintered base material to form a multilayer. shall be.

【0006】[0006]

【作用】本発明によれば焼結基材上にポリアセタ−ル樹
脂系組成物をコ−ティングし、このコ−ティングされた
焼結基材の樹脂組成物を加熱溶融状態でロ−ルにより焼
結基材に圧入するようにしたため焼結基材への充填が高
められる。
[Operation] According to the present invention, a polyacetal resin composition is coated on a sintered base material, and the coated resin composition on the sintered base material is heated and molten by rolling. Since it is press-fitted into the sintered base material, the filling of the sintered base material is increased.

【0007】以下、本発明の手段たる構成を作用と共に
更に詳しく説明すると、次の通りである。
[0007] Hereinafter, the configuration of the means of the present invention will be explained in more detail along with its operation.

【0008】本発明者等はポリアセタ−ル樹脂系組成物
と焼結基材の密着性不良について検討したところ、この
密着性不良は複層化時に起るケ−スが多く、その原因の
多くは焼結基材上の空気の追い出しが不十分なためであ
る。中でも従来の技術のシ−トの積層では、シ−トと焼
結基材との界面に空気が残留し、その部分は樹脂末充填
の密着不良の欠陥部として残ることがわかった。
[0008] The present inventors investigated the problem of poor adhesion between polyacetal resin compositions and sintered substrates, and found that this problem often occurs during multi-layering, and that many of the causes are This is because the air on the sintered base material is not sufficiently expelled. In particular, it has been found that in the conventional stacking of sheets, air remains at the interface between the sheet and the sintered base material, and this portion remains as a defective portion due to poor adhesion of the resin powder filling.

【0009】本発明では、ポリアセタ−ル樹脂系組成物
積層軸受材の一連の複層化処理において、空気残留の最
大の問題はロ−ル加工時に空気抜きが可能かどうかにあ
ると考え、その1つとして空気の出入が自由な粉末法を
検討した結果、その空気抜き効果が確認することができ
た。なお、粉末法では逆に多くの空気を含むため、ポリ
アセタ−ル樹脂は熱分解しやすいため、外観仕上り性か
らホモポリマ−型の適用は難かしく、コポリマ−型のポ
リアセタ−ル樹脂が好ましいことがわかった。
In the present invention, we believe that the biggest problem with residual air in a series of multi-layer treatments for polyacetal resin composition laminated bearing materials lies in whether or not it is possible to remove air during roll processing. As a result of investigating a powder method that allows air to freely enter and exit, we were able to confirm its effectiveness in removing air. However, since the powder method contains a lot of air and the polyacetal resin is easily thermally decomposed, it is difficult to apply a homopolymer type due to the appearance and finish, and a copolymer type polyacetal resin is preferable. Understood.

【0010】以下、図面により本発明の一つの実施例の
ポリアセタ−ル樹脂系組成物複層軸受の構成を説明する
The structure of a polyacetal resin composition multilayer bearing according to one embodiment of the present invention will be explained below with reference to the drawings.

【0011】図1は複層軸受材の縦断面図を示し、符号
1は裏金を示し、この裏金上に焼結された空孔率が30
〜50%の合金層2、その上にポリアセタ−ル樹脂系組
成物層3がある。裏金1は一般にはスチ−ルが使用され
、軸受材の機械的強度の保持と軸受面に発生する熱の放
散の機能をもつ。合金層2はポリアセタ−ル樹脂をアン
カ−効果で保持し、かつ軸受面に発生した熱を裏金に逃
す役割を担う。従って、合金層2は一般的な青銅あるい
は鉛青銅のいずれでも良いが、極度の摩耗で摺動面が合
金層まで達した場合の焼付きを考えた場合、耐焼付性の
良い後者の鉛青銅を用いることが好ましい。合金の形状
はイレギュラ−でも球状でも本発明の粉末積層法は対応
できるが、ポリアセタ−ル樹脂系組成物の圧入性の点で
は球状がより望ましく、その平均粒径は80〜150μ
mの範囲のものが好ましい。また、合金層2は200〜
400μmの範囲が好ましい。この理由は厚すぎると密
着不良を引起す恐れがあり、薄すぎると樹脂に対するア
ンカ−効果が不足するからである。
FIG. 1 shows a longitudinal cross-sectional view of a multilayer bearing material, and reference numeral 1 indicates a backing metal, and the porosity sintered on this backing metal is 30.
~50% alloy layer 2, on which is a polyacetal resin based composition layer 3. The back plate 1 is generally made of steel and has the functions of maintaining the mechanical strength of the bearing material and dissipating heat generated on the bearing surface. The alloy layer 2 serves to hold the polyacetal resin with an anchor effect and to release heat generated on the bearing surface to the backing metal. Therefore, the alloy layer 2 may be made of either general bronze or lead bronze, but considering the possibility of seizure if the sliding surface reaches the alloy layer due to extreme wear, the latter lead bronze has better seizure resistance. It is preferable to use The powder lamination method of the present invention can be applied to both irregular and spherical shapes of the alloy, but from the viewpoint of press-fitting of the polyacetal resin composition, spherical shapes are more desirable, and the average particle size is 80 to 150 μm.
A range of m is preferred. In addition, the alloy layer 2 has a molecular weight of 200~
A range of 400 μm is preferred. The reason for this is that if it is too thick, there is a risk of poor adhesion, and if it is too thin, the anchoring effect for the resin will be insufficient.

【0012】ポリアセタ−ル樹脂系組成物層3は軸受材
の摺動の機能を担うポイントとなる材料である。ポリア
セタ−ル樹脂はその構造からホモポリマ−型とコポリマ
−型に分類され、前者はホルムアルデヒドを出発原料と
して重合されたものであり、後者は例えばトリオキサン
とエチレンオキシドから合成されるコポリマ−である。 このコポリマ−型は分子の中間に「−C−C−」結合が
あるため、熱や化学薬品で解重合が始まっても、ポリオ
キシメチレン主鎖の中で最初に遭遇する「−C−C−」
結合で分解が停止する特性がある。本発明の粉末法では
分解を促進する空気(酸素)を多く含み、熱安定性の悪
いホモポリマ−型ポリアセタ−ル樹脂はいかなる温度〜
時間の条件下でも、ロ−ル成形後に樹脂面に分解ガスの
抜穴を残す。このため摺動性の面で問題が多く、本粉末
法では使用は困難である。一方、コポリマ−型ポリアセ
タ−ル樹脂も処理条件によっては分解の現象はあるが、
前述のような分子構造の特性から加熱温度170〜20
0℃、保持時間5〜20分の処理条件で良好な外観仕上
りを示しており、これを後記の実施例で詳述する。樹脂
層の厚みは特に制限はされないが、耐久性、放熱性そし
てコストなどから総合的にみると10〜400μmの範
囲にするのが望ましい。
The polyacetal resin composition layer 3 is a material that plays a key role in the sliding function of the bearing material. Polyacetal resins are classified into homopolymer types and copolymer types based on their structure; the former is polymerized using formaldehyde as a starting material, and the latter is a copolymer synthesized from, for example, trioxane and ethylene oxide. This copolymer type has a "-C-C-" bond in the middle of the molecule, so even if depolymerization begins due to heat or chemicals, the first "-C-C- -”
It has the property of stopping decomposition upon bonding. In the powder method of the present invention, a homopolymer type polyacetal resin containing a large amount of air (oxygen) that promotes decomposition and having poor thermal stability can be used at any temperature.
Even under long-term conditions, vent holes for decomposed gas are left on the resin surface after roll forming. Therefore, there are many problems in terms of sliding properties, and it is difficult to use this powder method. On the other hand, copolymer-type polyacetal resins may also decompose depending on the processing conditions;
Due to the characteristics of the molecular structure as mentioned above, the heating temperature is 170~20°C.
A good appearance finish was shown under the treatment conditions of 0° C. and a holding time of 5 to 20 minutes, and this will be explained in detail in Examples below. The thickness of the resin layer is not particularly limited, but from the viewpoint of durability, heat dissipation, cost, etc., it is preferably in the range of 10 to 400 μm.

【0013】本発明に係るコポリマ−型ポリアセタ−ル
樹脂に、摺動性を更に改良するために固体潤滑剤を加え
ることができる。固体潤滑剤としては無機系と有機系に
大別され、前者の例としては黒鉛(C)、二硫化モリブ
デン(MoS2)、酸化亜鉛(ZnO)、ふっ化カルシ
ウム(CaF2)、ヨウ化鉛(PbI2)、硫化カドミ
ウム(CdS)などが、後者の例としてはポリエチレン
、三ふっ化樹脂、PTFE(ポリテトラフルオロエチレ
ン)などが挙げられる。なお、ポリアセタ−ル樹脂は酸
あるいはアルカリが存在すると熱分解を起しやすくなる
ため、例えば、MoS2あるいはPbI2を配合する場
合、その配合量は樹脂100重量部に対し2重量部以下
とすることが好ましい。
A solid lubricant can be added to the copolymer-type polyacetal resin according to the present invention in order to further improve sliding properties. Solid lubricants are broadly classified into inorganic and organic types; examples of the former include graphite (C), molybdenum disulfide (MoS2), zinc oxide (ZnO), calcium fluoride (CaF2), and lead iodide (PbI2). ), cadmium sulfide (CdS), etc.; examples of the latter include polyethylene, trifluoride resin, PTFE (polytetrafluoroethylene), etc. Note that polyacetal resin tends to undergo thermal decomposition in the presence of acid or alkali, so for example, when MoS2 or PbI2 is blended, the blending amount should be 2 parts by weight or less per 100 parts by weight of resin. preferable.

【0014】本発明に用いるポリアセタ−ル樹脂は結晶
性が高く、かつガラス転移温度が高いことから常温での
粉砕も可能であるが、常温粉砕では粉砕時の発生熱によ
る化学的変質などが懸念されるため低温粉砕が望ましい
The polyacetal resin used in the present invention has high crystallinity and a high glass transition temperature, so it can be pulverized at room temperature. However, when pulverized at room temperature, there are concerns about chemical deterioration due to the heat generated during pulverization. Therefore, low-temperature pulverization is desirable.

【0015】表1は液体チッ素を用い、−196℃で粉
砕した粉末のふるい目と収率の関係を示す実験結果であ
る。粒径が細かくなるにつれて収率が悪くなり、割高と
なることを示している。例えば400メッシュのふるい
目では収率は僅か18wt%である。この結果より、コ
スト的にはより粒径の大きい粉末を用いることが望まし
いことが判る。
[0015] Table 1 shows the experimental results showing the relationship between the sieve size and yield of powder ground at -196°C using liquid nitrogen. This shows that as the particle size becomes finer, the yield becomes worse and the price becomes higher. For example, with a 400 mesh sieve, the yield is only 18 wt%. From this result, it can be seen that it is desirable to use powder with a larger particle size in terms of cost.

【0016】[0016]

【表1】[Table 1]

【0017】表1で得られた各粉末に固体潤滑剤として
例えばPbI2を加え、焼結基材への充填性と外観仕上
り(色むらの有無)性を評価したところ、本発明に用い
る樹脂粉末の粒径は495μm以下、望ましくは295
μm以下であることがわかった。
For example, PbI2 was added as a solid lubricant to each of the powders obtained in Table 1, and the filling properties into the sintered base material and the appearance finish (presence or absence of color unevenness) were evaluated. The particle size is 495 μm or less, preferably 295 μm or less.
It was found that it was less than μm.

【0018】[0018]

【実施例】以下実施例により本発明法を説明する。[Example] The method of the present invention will be explained by the following example.

【0019】実施例1.ホモポリマ−型ポリアセタ−ル
樹脂(旭化成工業(株)製商品名「テナック4010」
)およびコポリマ−型ポリアセタ−ル樹脂(旭化成工業
(株)製商品名「テナックC4510」)のペレットを
−196℃で低温粉砕し、これを80メッシュのふるい
で分級して粒径が175μm以下の微粉末を得た。 次に、この微粉末に固体潤滑剤としてヨウ化鉛(PbI
2)をポリアセタ−ル樹脂100重量部に対して2重量
部配合し、高速ミキサ−で10分間混合分散をして2種
の黄色のコ−ティング用の微粉樹脂組成物を得た。この
微粉末を巾150mm、長さ250mmの球状鉛青銅(
(Cu85wt%、Sn10wt%、Pb5wt%)合
金を空孔率40%、厚さ200μmで焼結した焼結基材
(総合厚0.98mm)上に散布し、ガラス棒で一様に
ならし、1mm厚のコ−ティング層とした。このコ−テ
ィング板を表2ならびに表3の条件で加熱炉で加熱をし
、処理後直ちに加熱炉より取り出し、図2に示す説明図
のように上下のロ−ル6、6′間に焼結基材4上にポリ
アセタ−ル調製粉5を散布したコ−ティング板を圧入処
理をして積層体7を得た。
Example 1. Homopolymer type polyacetal resin (product name: “Tenac 4010” manufactured by Asahi Kasei Industries, Ltd.)
) and copolymer-type polyacetal resin (product name "Tenac C4510" manufactured by Asahi Kasei Industries, Ltd.) were cryogenically ground at -196°C, and then classified using an 80-mesh sieve to obtain particles with a particle size of 175 μm or less. A fine powder was obtained. Next, lead iodide (PbI) is added to this fine powder as a solid lubricant.
2 parts by weight of 2) were blended with 100 parts by weight of polyacetal resin and mixed and dispersed for 10 minutes using a high speed mixer to obtain two types of yellow fine powder resin compositions for coating. This fine powder was made into a spherical lead bronze with a width of 150 mm and a length of 250 mm (
(Cu85wt%, Sn10wt%, Pb5wt%) alloy was sprinkled on a sintered base material (total thickness 0.98mm) with a porosity of 40% and a thickness of 200μm, and was evenly leveled with a glass rod. The coating layer was 1 mm thick. This coated plate was heated in a heating furnace under the conditions shown in Tables 2 and 3. Immediately after the treatment, it was taken out of the heating furnace and heated between upper and lower rolls 6 and 6' as shown in the explanatory diagram in Figure 2. A laminate 7 was obtained by press-fitting a coating plate on which polyacetal preparation powder 5 was sprinkled onto a bonding base material 4.

【0020】表2に示す結果のようにホモポリマ−型ポ
リアセタ−ル樹脂はいかなる温度下でも熱分解を起して
樹脂面にガスの抜穴が残り実用に供し得ない。一方、コ
ポリマ−型ポリアセタ−ル樹脂も過度の高温あるいは長
時間熱処理をするとホモポリマ−型のものと同様の現象
となるが、温度と時間を所定条件に設定すれば外観仕上
りの良好な複層材が得られることが判った。なお、表2
ならびに表3に用いた樹脂の融点はホモポリマ−型のも
のは179℃、コポリマ−型のものは167℃であった
As shown in Table 2, the homopolymer type polyacetal resin undergoes thermal decomposition at any temperature, leaving gas vent holes on the resin surface, making it unsuitable for practical use. On the other hand, if copolymer-type polyacetal resin is heat-treated at excessively high temperatures or for a long time, it will suffer from the same phenomenon as homopolymer-type polyacetal resin, but if the temperature and time are set to the specified conditions, multilayer materials with a good external finish can be produced. was found to be obtained. In addition, Table 2
The melting points of the resins used in Table 3 were 179°C for the homopolymer type and 167°C for the copolymer type.

【0021】[0021]

【表2】[Table 2]

【0022】[0022]

【表3】[Table 3]

【0023】実施例2.比較例 表1の方法で得られたコポリマ−型ポリアセタ−ル樹脂
粉末(旭化成工業(株)製商品名「テナックC4510
」)にそれぞれ樹脂100重量部に対してヨウ化鉛(P
bI2)を2重量部を配合し、実施例1と同様の方法で
分散混合し、11種の黄色のコ−ティング用の微粉樹脂
組成物を得た。一方、比較例として、上記と同一の樹脂
ペレットにヨウ化鉛を2重量部配合し、押出機により溶
融ブレンド法で厚さ0.4mmの黄色のフィルムを得た
。次いで、これらの粉末とフィルムを実施例1と同一の
基材にのせ、190℃×10分間加熱炉で熱処理したの
ち、直ちに取り出し、実施例1と同一方法でロ−ルにか
け複層化した。樹脂の焼結基材への充填性ならびに外観
の仕上り性(PbI2の分散度合)を基準として評価し
た結果を表4に示す。粉末法においてはより微粉ほど充
填性も良く外観の仕上りも良くなる傾向にあるが、実用
上は粒径が495μm以下、好ましくは295μm以下
で良いことが判る。一方、フィルムの積層では、溶融ブ
レンドにより外観仕上り性は極めてよく、PbI2の分
散性は良好であるが、半面樹脂の焼結基材への充填性は
必ずしも良好とは言えず、密着性に不安が残る。
Example 2. Comparative Example Copolymer-type polyacetal resin powder obtained by the method shown in Table 1 (trade name: ``Tenac C4510'' manufactured by Asahi Kasei Industries, Ltd.)
), lead iodide (P) per 100 parts by weight of resin, respectively.
2 parts by weight of bI2) were blended and dispersed and mixed in the same manner as in Example 1 to obtain 11 types of yellow fine powder resin compositions for coating. On the other hand, as a comparative example, 2 parts by weight of lead iodide was blended into the same resin pellets as above, and a yellow film with a thickness of 0.4 mm was obtained by melt blending using an extruder. Next, these powders and films were placed on the same substrate as in Example 1, heat treated in a heating furnace at 190°C for 10 minutes, immediately taken out, and rolled in the same manner as in Example 1 to form a multilayer structure. Table 4 shows the results of evaluation based on the filling properties of the resin into the sintered base material and the appearance finish (degree of dispersion of PbI2). In the powder method, there is a tendency that the finer the powder, the better the filling properties and the better the appearance finish, but in practice it is understood that the particle size should be 495 μm or less, preferably 295 μm or less. On the other hand, in film lamination, the appearance finish is extremely good due to melt blending, and the dispersibility of PbI2 is good, but the filling of the resin into the sintered base material is not necessarily good, and there are concerns about adhesion. remains.

【0024】[0024]

【表4】[Table 4]

【0025】実施例3.表1の方法で得られたコポリマ
−型ポリアセタ−ル樹脂粉末(旭化成工業(株)製商品
名「テナックC4510」)99重量部とヨウ化鉛(P
bI2)1重量部とを配合した以外は実施例1と同様に
行ない黄色のコ−ティング用微粉樹脂組成物を得た。次
いで、この樹脂組成物を処理時間と温度を変えた以外は
実施例1と同様に行なった結果を表5ならびに図3に示
した。表5ならびに図3から明らかなように温度が17
0℃から200℃に高くなると処理時間が短時間でよい
ことがわかった。なお、樹脂の加熱温度が160℃では
融点以下であるため、樹脂が不溶融若しくは半溶融とな
り、複層化は不可能であった。また、樹脂の加熱温度が
210℃では溶融と熱分解との温度が近接し複層化は困
難であった。
Example 3. 99 parts by weight of copolymer-type polyacetal resin powder (trade name "Tenac C4510" manufactured by Asahi Kasei Corporation) obtained by the method shown in Table 1 and lead iodide (P
A yellow fine powder resin composition for coating was obtained in the same manner as in Example 1 except that 1 part by weight of bI2) was blended. Next, this resin composition was treated in the same manner as in Example 1 except that the treatment time and temperature were changed, and the results are shown in Table 5 and FIG. As is clear from Table 5 and Figure 3, the temperature is 17
It has been found that when the temperature rises from 0°C to 200°C, the processing time can be shortened. Note that since the heating temperature of the resin is 160° C., which is below the melting point, the resin becomes unmolten or semi-molten, making it impossible to form multiple layers. Further, when the heating temperature of the resin was 210° C., the melting and thermal decomposition temperatures were close to each other, making it difficult to form multiple layers.

【0026】[0026]

【表5】[Table 5]

【0027】[0027]

【発明の効果】以上詳しく説明したように、本発明は裏
金とこの裏金上に焼結合金層とから成る焼結基材上に粒
径が295μm以下のポリアセタ−ル樹脂系組成物をコ
−ティングし、次いで、このコ−ティングされた焼結基
材のポリアセタ−ル樹脂系組成物を加熱溶融状態で上下
ロ−ル間を通し焼結基材に圧入して複層化することを特
徴とする。
Effects of the Invention As explained in detail above, the present invention provides a method for coating a polyacetal resin composition with a particle size of 295 μm or less on a sintered base material consisting of a backing metal and a sintered metal layer on the backing metal. Then, the polyacetal resin composition of the coated sintered base material is heated and molten and passed between upper and lower rolls and press-fitted into the sintered base material to form a multilayer. shall be.

【0028】本発明によれば、従来のシ−トあるいはフ
ィルムによる積層法を粉末法に変えたため、樹脂系組成
物の焼結基材への充填性がより完全なものとなり密着性
に優れた安定した品質の製品を顧客に提供することがで
き、また、粉末同志を機械的に極く短時間でブレンドす
ることにより所定の材料が得られるため設備投資も少額
で済み、押出成形機でフィルムとする必要もないため、
ランニングコストも安く済み、低コストの製品を顧客に
提供できる。
According to the present invention, since the conventional sheet or film lamination method has been changed to a powder method, the resin composition can be more completely filled into the sintered base material, resulting in excellent adhesion. We are able to provide products of stable quality to our customers, and because the specified material can be obtained by mechanically blending powders together in a very short time, capital investment is also small. Since there is no need to
Running costs are also low, allowing us to provide customers with low-cost products.

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

【図1】本発明法の一つの実施例のポリアセタ−ル樹脂
系組成物複層軸受材の縦断面図である。
FIG. 1 is a longitudinal sectional view of a multilayer bearing material made of a polyacetal resin composition according to one embodiment of the method of the present invention.

【図2】本発明法のポリアセタ−ル樹脂系組成物の焼結
基材への圧入状態を示す説明図である。
FIG. 2 is an explanatory diagram showing a state in which a polyacetal resin composition according to the present invention is press-fitted into a sintered base material.

【図3】本発明法のポリアセタ−ルの処理条件を示す温
度と時間との関係を示すグラフである。
FIG. 3 is a graph showing the relationship between temperature and time showing the processing conditions for polyacetal according to the present invention.

【符号の説明】[Explanation of symbols]

1  裏金 2  合金層 3  ポリアセタ−ル樹脂系組成物層 4  焼結基材 5  ポリアセタ−ル調整粉 7  複層体 1 Secret money 2 Alloy layer 3 Polyacetal resin composition layer 4 Sintered base material 5 Polyacetal adjusted powder 7 Composite layer

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】  裏金とこの裏金上に焼結合金層とから
成る焼結基材上に粒径が295μm以下のポリアセタ−
ル樹脂系組成物をコ−ティングし、次いで、このコ−テ
ィングされた焼結基材のポリアセタ−ル樹脂系組成物を
170〜200℃の条件で加熱溶融させ、この状態で上
下ロ−ル間を通し焼結基材に圧入して複層化することを
特徴とするポリアセタ−ル樹脂系組成物複層軸受材の製
造方法。
Claim 1: A sintered base material consisting of a back metal and a sintered metal layer on the back metal, and a polyaceter with a particle size of 295 μm or less.
The polyacetal resin composition of the coated sintered base material is then heated and melted at 170 to 200°C, and in this state upper and lower rolls are applied. A method for producing a multilayer bearing material made of a polyacetal resin composition, which comprises press-fitting a polyacetal resin composition into a sintered base material to form a multilayer bearing material.
【請求項2】  ポリアセタ−ル樹脂がコポリマ−型の
樹脂である請求項1記載のポリアセタ−ル樹脂系組成物
複層軸受材の製造方法。
2. The method for producing a polyacetal resin composition multilayer bearing material according to claim 1, wherein the polyacetal resin is a copolymer type resin.
【請求項3】  焼結合金が銅、スズ、鉛から成る鉛青
銅で、かつ平均粒径が80〜150μmである請求項1
又は2記載のポリアセタ−ル樹脂系組成物複層軸受材の
製造方法。
[Claim 3] Claim 1, wherein the sintered alloy is lead bronze consisting of copper, tin, and lead, and has an average grain size of 80 to 150 μm.
Or the method for producing a polyacetal resin composition multilayer bearing material according to 2.
JP3025536A 1991-01-25 1991-01-25 Manufacture of double-layered bearing material made of polyacetal resin composition Pending JPH04351543A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3025536A JPH04351543A (en) 1991-01-25 1991-01-25 Manufacture of double-layered bearing material made of polyacetal resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3025536A JPH04351543A (en) 1991-01-25 1991-01-25 Manufacture of double-layered bearing material made of polyacetal resin composition

Publications (1)

Publication Number Publication Date
JPH04351543A true JPH04351543A (en) 1992-12-07

Family

ID=12168736

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3025536A Pending JPH04351543A (en) 1991-01-25 1991-01-25 Manufacture of double-layered bearing material made of polyacetal resin composition

Country Status (1)

Country Link
JP (1) JPH04351543A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04133019U (en) * 1991-05-31 1992-12-10 エヌテイエヌ株式会社 composite bearing

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53113876A (en) * 1977-03-15 1978-10-04 Daido Metal Co Ltd Metallbacked slideerequired member
JPS61171919A (en) * 1985-12-28 1986-08-02 Taiho Kogyo Co Ltd Manufacture method of composite friction member

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53113876A (en) * 1977-03-15 1978-10-04 Daido Metal Co Ltd Metallbacked slideerequired member
JPS61171919A (en) * 1985-12-28 1986-08-02 Taiho Kogyo Co Ltd Manufacture method of composite friction member

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04133019U (en) * 1991-05-31 1992-12-10 エヌテイエヌ株式会社 composite bearing

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