JPS6362852A - Ferrous sintered sliding material for current collection - Google Patents
Ferrous sintered sliding material for current collectionInfo
- Publication number
- JPS6362852A JPS6362852A JP20721886A JP20721886A JPS6362852A JP S6362852 A JPS6362852 A JP S6362852A JP 20721886 A JP20721886 A JP 20721886A JP 20721886 A JP20721886 A JP 20721886A JP S6362852 A JPS6362852 A JP S6362852A
- Authority
- JP
- Japan
- Prior art keywords
- sintered alloy
- titanium
- sliding material
- trolley wire
- current
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 41
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 title abstract description 5
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 22
- 239000000956 alloy Substances 0.000 claims abstract description 22
- 150000004767 nitrides Chemical class 0.000 claims abstract description 17
- 229910001200 Ferrotitanium Inorganic materials 0.000 claims abstract description 15
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims abstract description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 15
- 229910052742 iron Inorganic materials 0.000 claims description 8
- 239000011148 porous material Substances 0.000 abstract description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 1
- 239000010936 titanium Substances 0.000 description 19
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 17
- 229910052719 titanium Inorganic materials 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 230000013011 mating Effects 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- 239000000314 lubricant Substances 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000005245 sintering Methods 0.000 description 6
- 238000012360 testing method Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000005299 abrasion Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000005121 nitriding Methods 0.000 description 3
- GIMSJJHKKXRFGV-BYPJNBLXSA-N 4-amino-1-[(2r,3s,4r,5r)-3-fluoro-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodopyrimidin-2-one Chemical compound C1=C(I)C(N)=NC(=O)N1[C@H]1[C@@H](F)[C@H](O)[C@@H](CO)O1 GIMSJJHKKXRFGV-BYPJNBLXSA-N 0.000 description 2
- 102000002322 Egg Proteins Human genes 0.000 description 2
- 108010000912 Egg Proteins Proteins 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 210000003278 egg shell Anatomy 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910017135 Fe—O Inorganic materials 0.000 description 1
- 229910011208 Ti—N Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- -1 alcone Substances 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Current-Collector Devices For Electrically Propelled Vehicles (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】 本発明は、鉄系焼結集電摺動材料に関する。[Detailed description of the invention] The present invention relates to a ferrous sintered current collector sliding material.
集電摺動材料に要求される性質として、例えば相手材で
あるトロリー線に対して攻撃性の少ないこと、十分々耐
摩耗性を有すること、機械的な強度を具備し、電気抵抗
の小さいことが挙げられる。Properties required of current collector sliding materials include, for example, low aggressiveness against the mating material, the trolley wire, sufficient abrasion resistance, mechanical strength, and low electrical resistance. can be mentioned.
特にト0り一線の保守、寿命などを考えると、攻撃性の
少ないことが最も重要な性質となる。攻撃性を少なくす
るKは材料の硬すを下げ、潤滑性に富むことが絶対的に
必要な条件となる。材料が軟質であるということと潤滑
性に富むこととは傾向として一致するので好都合である
。すなわち潤滑剤を添加した場合、材料が軟質であれば
あるほど潤滑剤が突出しやすく、従って相手材と潤滑材
の接触する機会が増加するからである。しかしながら従
来の集電摺動用焼結合金はFeあるいはCMを主成分と
する基地中に耐摩性を向上するために各種の金属を添加
しておシ、これらの方法によればいずれの場合も金属の
基地中への拡散が著しく、材質の硬化を伴って必然的に
潤滑性も減少し、結果的にトロリー線に対する攻撃性が
大となる。また電気抵抗は金属の添加とともに増加する
ので、この方法によれば潤滑剤として用いる元素の添加
量もかなシ少1iK制限され、潤滑性の低下がさらに助
長される結果となる。さらに電気抵抗率の増加とあいま
って、これらの元素は機械強度のうち、特にiIi撃値
を極端に低下させる。潤滑剤として用いる元素も同様に
作用するので、機械特性の而からも添加量に制限を受け
る。すなわち、主として耐摩耗性を向上させる目的で添
加する金属はトロリー線に対する攻撃性、電気抵抗率、
l1lI撃値などほとんどの因子に悪影響を及ぼし、こ
のことが従来焼結集電摺動材料において耐摩耗性と潤滑
性の双方を兼備することは予盾するとされてきた原因で
ある。Especially when considering long-term maintenance and lifespan, the most important characteristic is less aggressiveness. K, which reduces aggressiveness, lowers the hardness of the material, and it is absolutely necessary that it has good lubricity. It is advantageous that the material is soft and has good lubricity, since these tend to coincide. That is, when a lubricant is added, the softer the material, the more likely the lubricant will protrude, and therefore the chance of the lubricant coming into contact with the other material increases. However, in conventional sintered alloys for current collector sliding, various metals are added to the base mainly composed of Fe or CM to improve wear resistance. Diffusion into the base is significant, and with the hardening of the material, the lubricity inevitably decreases, resulting in increased aggressiveness against the trolley wire. Furthermore, since the electrical resistance increases with the addition of metal, this method limits the amount of the element used as a lubricant to a very small 1iK, resulting in further deterioration of lubricity. Furthermore, together with the increase in electrical resistivity, these elements extremely reduce the mechanical strength, particularly the iIi impact value. Elements used as lubricants also act in the same way, so the amount added is limited by mechanical properties. In other words, metals added mainly for the purpose of improving wear resistance improve the aggressiveness of trolley wires, electrical resistivity,
This has an adverse effect on most factors such as the l1lI impact value, and this is the reason why it has conventionally been said that it is necessary to have both wear resistance and lubricity in sintered current collector sliding materials.
本発明者は、上記した如き問題点に鑑みて、耐摩耗性及
び潤滑性の双方を兼備する集電摺動材料を見出すべく鋭
意研究を重ねた結果、チタン窒化物又はフェロチタン窒
化物を一定量含有する鉄系焼結合金が所期の効果を奏す
ることを見出し、特許出願を行なった(特願昭55〜5
8490号)。In view of the above-mentioned problems, the inventors of the present invention have conducted intensive research to find a current collector sliding material that has both wear resistance and lubricity. He discovered that iron-based sintered alloys containing a large amount of
No. 8490).
鉄系焼結合金の空孔部に一定量の鉛を溶浸させる場合に
は、集電摺動材料として要求される緒特性が低下するこ
となく、更にトロリー線に対する攻撃性が着るしく小さ
くなることを見出し、ここに窒化物を0.5〜15重量
%含有する鉄系焼結合金100重量部、及び鉛5〜20
重量部からなることを特徴とする鉄系焼結集電摺動材料
に係る。When a certain amount of lead is infiltrated into the pores of the iron-based sintered alloy, the wire properties required as a current collector sliding material will not deteriorate, and the aggressiveness against trolley wires will be significantly reduced. 100 parts by weight of an iron-based sintered alloy containing 0.5 to 15% by weight of nitrides and 5 to 20 parts by weight of lead.
The present invention relates to an iron-based sintered current collector sliding material characterized in that it consists of a weight part.
本発明においてチタンあるいはフよりチタンは予め窒化
処理して添加する方法と、焼結中に窒化する方法とがあ
る。チタンあるいはフェロチタンは容易に窒化されるが
、これらの窒化物は安定でアシ、いったん窒化されると
、なかなか内部にまで窒化は進行しないので窒化された
粉末粒子は表面から厚さ約2μ以下の非常に硬い窒化層
と内部が軟かい純チタンあるいは純フエOチタンから形
成される。この様な窒化物では、実際に耐摩剤として作
用する部分はチタン又はフェロチタンの表面に存在する
薄い窒化層と相手材の接触界面である。したがって摺動
面におけるチタンの窒化層およびフェロチタンの窒化層
の占める面積の割合は極めて微々たるもので1さらに摺
動時にこれらの窒化層が摩耗粉となって欠損し摺動面を
移動するときも、窒化層がせいぜい約2μと非常に薄い
ため相手材への攻撃性は少ない。この窒化層は非常に硬
く、チタン又はフェロチタン粒子の極く表面にほぼ一様
の厚みでちょうど卵の殻のような形で存在し、ミクロ的
にみて摺動面から内部へと連続している。本発明品が摺
動状態にあるとき、この窒化層が摩耗するためにはいわ
ゆる上記の卵の殻を破壊するに足りる剪断応力が必要と
なるが、この窒化層は内部の純チタンあるいは純フエO
チタンとは当然のことながらしっかりと結合しておシ、
破壊して摺動面外へ持ち去ることはむずかしい。また相
手材の摺動面が荒れた面であるとき、窒化層が徐々に破
壊されていくJ4耗でなく、耐摩粒子全体がマトリック
スから離脱する、いわゆる“欠は落ち現象 が生じる危
惧があるが、これは耐摩粒子としてフェロチタンの窒化
物を用いることによって解決される。フェロチタンを窒
化処理すると窒化されやすいTi が優先窒化し、Ft
は窒化されていないので、これをFt を主成分とす
る基地中に添加するとフェロチタンのFz のみがマト
リックスに拡散し、結合が強固となるからである。チタ
ンの窒化物はほとんどマトリックス中に拡散せず、フェ
ロチタンについても上記の通りなので、マトリックス自
体は金属固溶による硬化はほとんどみられない。このよ
うに薄い窒化層を主として耐摩剤として用い、マトリッ
クスが軟かいことによって本発明品は相手材を攻撃する
ことが少ない。チタニア、シソ力などの酸化物もチタン
の窒化層と同様、硬い物質として知られているが、これ
らを耐摩粒子として用いた場合、粒子全体が硬いので破
壊して摩耗する現象よりはむしろ“欠は落ち現象 によ
る摩耗の方が起こり易く、いずれの場合もその摩耗粉は
硬く粗いので相手材を攻撃し、またマトリックスとの結
合がはかれないので耐摩剤としての効果は期待できない
。In the present invention, there is a method in which titanium or titanium is added after being nitrided in advance, and a method in which titanium is added during sintering. Titanium or ferrotitanium is easily nitrided, but these nitrides are stable and nitrided, and once nitrided, the nitridation does not progress to the inside easily. It is made of a very hard nitride layer and a soft interior made of pure titanium or pure Fe-O titanium. In such a nitride, the part that actually acts as an anti-wear agent is the contact interface between the thin nitride layer existing on the surface of titanium or ferrotitanium and the mating material. Therefore, the ratio of the area occupied by the titanium nitride layer and the ferrotitanium nitride layer on the sliding surface is extremely small. 1Furthermore, during sliding, these nitride layers become abrasion particles that break off and move on the sliding surface. However, since the nitride layer is very thin, at most about 2 μm, it is less likely to attack the mating material. This nitrided layer is very hard and exists on the very surface of the titanium or ferrotitanium particles with an almost uniform thickness and in the shape of an eggshell.From a microscopic perspective, it continues from the sliding surface to the inside. There is. When the product of the present invention is in a sliding state, in order for this nitride layer to wear out, a shearing stress sufficient to destroy the so-called eggshell described above is required, but this nitride layer is O
Naturally, it is tightly bonded to titanium.
It is difficult to destroy and remove it from the sliding surface. In addition, when the sliding surface of the mating material is rough, there is a risk that the so-called "chip drop phenomenon" will occur, in which the entire wear-resistant particles separate from the matrix, rather than J4 wear, in which the nitrided layer is gradually destroyed. This problem can be solved by using ferrotitanium nitride as wear-resistant particles.When ferrotitanium is nitrided, Ti, which is easily nitrided, is preferentially nitrided, and Ft
This is because, since it is not nitrided, when it is added to a matrix mainly composed of Ft, only Fz of ferrotitanium will diffuse into the matrix, and the bond will become stronger. Since titanium nitride hardly diffuses into the matrix, and the same is true for ferrotitanium as described above, the matrix itself is hardly hardened by metal solid solution. Since the thin nitride layer is used primarily as an anti-wear agent and the matrix is soft, the product of the present invention is less likely to attack the mating material. Oxides such as titania and titanium are also known to be hard materials, as is the nitride layer of titanium, but when these are used as wear-resistant particles, the entire particle is hard, so rather than breaking and wearing out, the phenomenon of "breakage" occurs. Wear caused by the flaking phenomenon is more likely to occur, and in either case, the wear powder is hard and coarse and attacks the mating material, and cannot be expected to be effective as an anti-wear agent because it cannot be bonded to the matrix.
本発明における上記チタンの窒化物もしくはフ工Oチタ
ンの窒化物としては例えば約100〜200メツシユの
粒子を用いるのが好ましい。また実際に耐摩剤として作
用する部分は粒子のごく表面に限られるから粒度を調整
することによυ任意の耐摩耗特性が得られる。チタン及
び/又はフ工0チタンの量は約焼結合金中0.5〜15
重黛%が好ましい。この範囲では十分な耐摩性、潤滑性
、機械的強度が得られる。In the present invention, it is preferable to use particles of about 100 to 200 mesh as the titanium nitride or the titanium nitride. Furthermore, since the part that actually acts as an anti-wear agent is limited to the very surface of the particle, any desired wear-resistant property can be obtained by adjusting the particle size. The amount of titanium and/or free titanium is approximately 0.5 to 15% in the sintered alloy.
Heavy weight percentage is preferred. In this range, sufficient wear resistance, lubricity, and mechanical strength can be obtained.
金に、更に鉛を溶浸略せることが必要である。鉛を溶浸
させることによシ、焼結合金の空孔部に鉛が侵入し、保
持されて集YIi摺動材料のすシ板特性の改善、特にト
ロリー線の摩耗の軽減が図られる。It is necessary to infiltrate gold with lead. By infiltrating lead, the lead enters into the pores of the sintered alloy and is retained, thereby improving the plate characteristics of the YIi sliding material and, in particular, reducing the wear of the trolley wire.
鉛の含浸社は、上記したチタン窒化物またはフェロチタ
ン窒化物を含む焼結合金100重量部に対して、5〜2
0重ffi部とすることが適当である。Lead Impregnation Co., Ltd. uses 5 to 2 parts by weight of the sintered alloy containing titanium nitride or ferrotitanium nitride as described above.
It is appropriate to use a 0-fold ffi section.
鉛量が5重量部未満では、トロリー線に対する摩耗軽減
効果が不足し、一方20重量部を上回ると集電摺動材料
としての耐摩耗性や機械的特性が低下するので好ましく
ない。If the amount of lead is less than 5 parts by weight, the effect of reducing wear on the trolley wire will be insufficient, while if it exceeds 20 parts by weight, the abrasion resistance and mechanical properties of the current collector sliding material will deteriorate, which is not preferable.
本発明の焼結集電摺動材料は上記のチタンの窒化物及び
/又はフよりチタンの窒化物を含む焼結合金に、鉛を溶
浸させることを特徴とするもので、その他の構成は通常
の焼結集電摺動材料と同じで良い。従って通常の基地成
分としてFt 又はFtt主成分とする合金を用いるこ
とができる。また本発明では機械特性と電気特性を所定
の値に保持する程度の最低限度の鼠で、通常焼結集電摺
動材料に添加される金属等を添加することができる。The sintered current collector sliding material of the present invention is characterized by infiltrating the sintered alloy containing titanium nitride and/or titanium nitride with lead, and other configurations are normal. It can be the same as the sintered current collector sliding material. Therefore, Ft or Ftt-based alloys can be used as the usual base component. Further, in the present invention, metals and the like that are normally added to sintered current collector sliding materials can be added to the material with the minimum amount necessary to maintain the mechanical properties and electrical properties at predetermined values.
これらの金属の例としては例えばNi、Mσ、 Cm、
Fz。Examples of these metals include Ni, Mσ, Cm,
Fz.
Cr、Pのような金属及びこれら金属の合金、代表例と
LテハFtMo、 FtCr、 CmCr等のものを例
示でき、これらは少なくとも1種以上添加でき通常焼結
合金巾約O1a〜1ト1%の範囲で用いられるが、本発
明ではこれら金属の量を従来のものに比して少なくする
ことが可能で通常約0.8〜lQm/%の範囲で用いる
のが特に好ましい0
本発明では上記以外に必要に応じてWS2. MρS2
゜C(黒鉛)、ボロンナイトライド等の潤滑剤、Ha、
Cr、 F gets 、 F tc r等の耐摩剤
などを添加することもできる。Typical examples of metals such as Cr, P and alloys of these metals include LTE, FtMo, FtCr, CmCr, etc., and at least one of these can be added. However, in the present invention, it is possible to reduce the amount of these metals compared to conventional ones, and it is particularly preferable to use them usually in the range of about 0.8 to 1Qm/%. WS2. as necessary. MρS2
°C (graphite), lubricants such as boron nitride, Ha,
Antiwear agents such as Cr, Fgets, Ftcr, etc. can also be added.
本発明の焼結集電摺動材料を得るには、まず上記基地成
分、金属成分及び必要に応じその他の添加剤を配合した
ものに、チタン及び/又はフェロチタンを予め窒化処理
して添加、成形して焼結することにより、或いは該チタ
ン及び/又はフェロチタンを未処理のまま添加して成形
後、窒素またはアン七ニアを含む雰囲気中で焼結して該
焼結中にチタン及び/又はフェロチタンを窒化すること
によシ焼結合金を形成させる。窒化処理を行うには上記
したように窒素ガス、窒素と水素の混合カス、アン七ニ
アガス、アン七ニア分解ガスなどの室紫またはアン七ニ
アを含む雰囲気中、とシわけ中性または還元性雰囲気中
で約600〜1800°Cで加熱するのが良い。成形は
約2.5〜7.51an / cd 。In order to obtain the sintered current collector sliding material of the present invention, first, titanium and/or ferrotitanium is added to a mixture of the base component, metal component, and other additives as necessary, after being nitrided in advance, and then molded. or by adding the titanium and/or ferrotitanium untreated and sintering it in an atmosphere containing nitrogen or ferrotitanium during the sintering. A sintered alloy is formed by nitriding ferrotitanium. To carry out the nitriding treatment, as mentioned above, use nitrogen gas, a mixture of nitrogen and hydrogen, anhydrogen gas, anhydrogen decomposition gas, etc. in a neutral or reducing atmosphere containing purple or anhydrogen. It is preferable to heat at about 600 to 1800°C in an atmosphere. Molding is approximately 2.5-7.51 an/cd.
焼結は通常約750〜1300°Cで行うのが好ましい
。該焼結は窒化を同時に行うときは上記窒素またはアン
七ニアガスを含む雰囲気中で行う必要があるが、予め窒
化処理したチタン及び/又はフ工0チタンを用いる場合
は上記と同じ雰囲気を用いても良いが、これ以外にアル
コン、水素、ヘリウム等のガス或いは真空下の雰囲気で
焼結しても良い。Sintering is usually preferably carried out at a temperature of about 750-1300°C. When nitriding is performed at the same time, the sintering must be performed in an atmosphere containing nitrogen or annealing gas, but when using pre-nitrided titanium and/or untreated titanium, the same atmosphere as above must be used. However, in addition to this, sintering may be performed in a gas such as alcone, hydrogen, or helium, or in a vacuum atmosphere.
次いで、得られた焼結合金に所定鼠の鉛を溶浸させるこ
とによって本発明集電摺動材料が得られる。溶浸の方法
としては、例えば焼結合金上に所定重量の鉛片を載置し
、還元又は中性雰囲気中で1000〜1100℃に加熱
して、鉛を焼結合金の空孔部に侵入させればよい。Next, the current collector sliding material of the present invention is obtained by infiltrating the obtained sintered alloy with a predetermined amount of lead. As for the infiltration method, for example, a lead piece of a predetermined weight is placed on the sintered alloy and heated to 1000 to 1100°C in a reducing or neutral atmosphere to infiltrate the lead into the pores of the sintered alloy. Just let it happen.
以上のようにして得られる本発明の焼結集電摺動材料に
おいては1マトリツクスの硬すは純鉄焼結体以上の任意
の値のものを得ることができるが、機械強度、潤滑性、
相手材(例えばトロリー線)への攻撃性などの諸要件を
考慮すると、通常プリネル硬すで約50〜95、特には
約60〜80のものが好ましい。これらの硬すの範囲に
おいては添加した潤滑剤が十分その効果を発揮する。In the sintered current collector sliding material of the present invention obtained as described above, the hardness of one matrix can be any value higher than that of pure iron sintered material, but the mechanical strength, lubricity,
Considering various requirements such as aggressiveness to mating material (for example, trolley wire), a Purinel hardness of about 50 to 95, particularly about 60 to 80 is preferred. In these hardness ranges, the added lubricant can sufficiently exhibit its effect.
本発明集電摺動材料は、機械的強度、電気特性等に優れ
たものであって、更に耐摩耗性及び潤滑性が良好であシ
、特に相手材であるトロリー線に対する攻撃性が少ない
。The current collector sliding material of the present invention has excellent mechanical strength, electrical properties, etc., and also has good wear resistance and lubricity, and is particularly less aggressive against the mating material, the trolley wire.
以下に実施例を示して本発明の詳細な説明する。The present invention will be described in detail below with reference to Examples.
実施例1
第1表に焼結集電摺動材料の組成を示す。尚、表中のF
tTi −N、 Ti−Nは、pzTi又はTiをアン
上ニア中で1000°C1時間保持して窒化物が生成し
たものである。Example 1 Table 1 shows the composition of the sintered current collector sliding material. In addition, F in the table
tTi-N and Ti-N are nitrides produced by holding pzTi or Ti at 1000° C. for 1 hour in an annealer.
第1表の各成分(Ph を除く)を混合し、6〜7トン
/Cdで成形し、アン七ニア分解ガス中で1120℃で
90分間焼結させて、焼結合金を得た。本発明品1〜7
については、得られた焼結合金上に、所定量の鉛片を載
置して、アシtニア分解ガス雰囲気中で1080°Cで
90分間加熱して、焼結合金中に鉛を溶浸させた。The components listed in Table 1 (excluding Ph) were mixed, molded at 6 to 7 tons/Cd, and sintered at 1120° C. for 90 minutes in annealy cracked gas to obtain a sintered alloy. Invention products 1 to 7
For this, a predetermined amount of lead pieces was placed on the obtained sintered alloy, and heated at 1080°C for 90 minutes in an atmosphere of acitonia decomposition gas to infiltrate lead into the sintered alloy. I let it happen.
第 1 表
得られ九集電摺動材料の物理特性を第2表に、また耐摩
耗性試験結果を第8表に示す。Table 1 The physical properties of the nine current collector sliding materials obtained are shown in Table 2, and the results of the wear resistance test are shown in Table 8.
摩耗試験は得られたすシ板材から寸法形状1゜X25X
90mを切シ出し、集N摺動摩耗の試験片とした。試験
条件は押付力5kg/d、通電電流FiAC(21F)
100A、摺動速度ti 100 KM/にとし、試験
時間を5分間とした。相手側トロリー線は硬銅線を用い
、直径8851Mに巻き付は接触接面を6ff巾に仕上
げた架線構造とした。この場合、すシ板の偏心率を10
ffに設け、電車に於けるパンタグラフの使用条件に相
似とした。The wear test was carried out using the obtained shim board material with dimensions of 1° x 25 x
A length of 90 m was cut out and used as a test piece for N collecting sliding wear. Test conditions are pressing force 5kg/d, current FiAC (21F)
100A, sliding speed ti 100 KM/, and test time 5 minutes. The mating trolley wire was made of hard copper wire, and had an overhead wire structure with a diameter of 8851M and a winding contact surface with a width of 6ff. In this case, the eccentricity of the sushi board is 10
ff, similar to the usage conditions of pantographs on trains.
試料面状態、トロリー面状態の評価は次の通シである。The evaluation of the sample surface condition and trolley surface condition is as follows.
◎ 極めて良好 O良好
Δ やや不良 X 不良
第 2 表
第 8 表
以上の結果から明らかな様に、チタン窒化物又はフェロ
チタン窒化物を含有する鉄系焼結合金に、鉛を溶浸させ
た材料は、電気特性及び機械的強度ともに良好であシ、
集電摺動材料として使用した場合に、耐摩性に優れ、か
つトロリー線を損傷させることが少ないものである。◎ Very good O Good Δ Slightly poor has good electrical properties and mechanical strength,
When used as a current collector sliding material, it has excellent wear resistance and is less likely to damage the trolley wire.
(以 上)
代理人 弁理士 三 枝 英 二 、 ゛・1
614..1(The above) Agent: Patent attorney Eiji Saegusa, ゛・1
614. .. 1
Claims (1)
.5〜15重量%含有する鉄系焼結合金100重量部及
び鉛5〜20重量部からなることを特徴とする鉄系焼結
集電摺動材料。(1) Zero titanium nitride and/or ferrotitanium nitride
.. An iron-based sintered current collector sliding material comprising 100 parts by weight of an iron-based sintered alloy containing 5 to 15% by weight and 5 to 20 parts by weight of lead.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20721886A JPS6362852A (en) | 1986-09-03 | 1986-09-03 | Ferrous sintered sliding material for current collection |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20721886A JPS6362852A (en) | 1986-09-03 | 1986-09-03 | Ferrous sintered sliding material for current collection |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6362852A true JPS6362852A (en) | 1988-03-19 |
Family
ID=16536200
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20721886A Pending JPS6362852A (en) | 1986-09-03 | 1986-09-03 | Ferrous sintered sliding material for current collection |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6362852A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03207837A (en) * | 1990-01-10 | 1991-09-11 | Railway Technical Res Inst | Ferrous sintered current collecting-sliding material |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56153902A (en) * | 1980-04-30 | 1981-11-28 | Japanese National Railways<Jnr> | Sintered material for sliding current collector |
JPS59114125A (en) * | 1982-12-17 | 1984-07-02 | Kinugawa Rubber Ind Co Ltd | Center seal rubber for sashless vehicle |
JPS60215748A (en) * | 1984-04-07 | 1985-10-29 | Riken Corp | Wear-resistant sintered alloy |
JPS6119760A (en) * | 1984-07-06 | 1986-01-28 | Riken Corp | Abrasion resistant sintered alloy |
-
1986
- 1986-09-03 JP JP20721886A patent/JPS6362852A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56153902A (en) * | 1980-04-30 | 1981-11-28 | Japanese National Railways<Jnr> | Sintered material for sliding current collector |
JPS59114125A (en) * | 1982-12-17 | 1984-07-02 | Kinugawa Rubber Ind Co Ltd | Center seal rubber for sashless vehicle |
JPS60215748A (en) * | 1984-04-07 | 1985-10-29 | Riken Corp | Wear-resistant sintered alloy |
JPS6119760A (en) * | 1984-07-06 | 1986-01-28 | Riken Corp | Abrasion resistant sintered alloy |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03207837A (en) * | 1990-01-10 | 1991-09-11 | Railway Technical Res Inst | Ferrous sintered current collecting-sliding material |
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