JP2009013370A - Sliding structure - Google Patents

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JP2009013370A
JP2009013370A JP2007179794A JP2007179794A JP2009013370A JP 2009013370 A JP2009013370 A JP 2009013370A JP 2007179794 A JP2007179794 A JP 2007179794A JP 2007179794 A JP2007179794 A JP 2007179794A JP 2009013370 A JP2009013370 A JP 2009013370A
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sliding
lubricating oil
oil
film
acid
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JP5221067B2 (en
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Yoshio Fuwa
良雄 不破
Tokuji Umehara
徳次 梅原
Takayuki Nooiyama
貴行 野老山
Yuichiro Ogawa
雄一郎 小河
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Nagoya University NUC
Toyota Motor Corp
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Toyota Motor Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a sliding structure which can reduce a friction coefficient and improve a wear resistance, even under a severe sliding environment such as high surface pressure. <P>SOLUTION: The present invention relates to a sliding structure comprising: a pair of sliding members on at least one sliding surfaces of which among mutually sliding surfaces a hard carbon coating film is formed; and a lubricant existing between a pair of the sliding members, wherein the lubricant is a vegetable lubricant containing at least one of oleic acid, linoleic acid and linolenic acid. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、相互に摺動する摺動面のうち少なくとも一方の摺動面に硬質炭素被膜が形成された一対の摺動部材と、該一対の摺動部材の間に存在する潤滑油と、を備えた摺動構造に係り、特に、一対の摺動部材の摩擦係数の低減及び耐摩耗性の向上を図ることできる摺動構造に関する。   The present invention includes a pair of sliding members in which a hard carbon film is formed on at least one of the sliding surfaces that slide relative to each other, a lubricating oil present between the pair of sliding members, In particular, the present invention relates to a sliding structure capable of reducing the friction coefficient and improving the wear resistance of a pair of sliding members.

近年、機械を取り巻くエネルギー問題や環境問題に関心が集まっている。エネルギー源を石油や原子力に依存する現在社会において、エネルギー資源の枯渇は危惧すべき問題である。20世紀は大量生産・大量消費の時代であったが、21世紀は限りあるエネルギーをいかに効率よく使用するかが重要である。   In recent years, there has been an interest in energy issues and environmental issues surrounding machinery. In today's society, where energy sources depend on oil and nuclear power, the depletion of energy resources is a matter of concern. The 20th century was an era of mass production and mass consumption, but in the 21st century it is important to use limited energy efficiently.

機械におけるエネルギー損失の1つに摩擦損失がある。機械には、必ず摺動面が存在し摩擦が生じており、摩擦を減少させることはエネルギーの消費を減少させることに繋がる。摩擦の低減は潤滑油によって2面間の直接接触を妨げ、せん断抵抗を減少させることにより達成される。現在も多くの機械で潤滑油が使用され、潤滑油に関する研究は盛んに行われている。   One energy loss in machines is friction loss. A machine always has a sliding surface and generates friction, and reducing the friction leads to a reduction in energy consumption. Friction reduction is achieved by preventing direct contact between the two surfaces by the lubricant and reducing shear resistance. Many machines still use lubricating oil, and research on the lubricating oil is actively conducted.

一方、摩擦を低減させる材料として、非晶質炭素被膜、窒化炭素被膜、ダイヤモンド被膜などの硬質炭素被膜が注目されており、該被膜を摺動面に適用することにより摺動部材の摩擦の低減・耐摩耗性の向上が期待されている。   On the other hand, hard carbon coatings such as amorphous carbon coatings, carbon nitride coatings, and diamond coatings are attracting attention as materials for reducing friction, and the friction of sliding members can be reduced by applying these coatings to sliding surfaces.・ Improved wear resistance.

しかし、前記機械を構成する部品として、例えば自動車エンジン部品は、近年、高出力及び高回転による高性能化が著しい。これに伴い、エンジンで使用される摺動部材において、摺動面に前記硬質炭素被膜を適用したのみでは、その性能向上は限界がある。よって、摺動部材と潤滑油の最適な組み合わせを考慮して、より摺動特性に優れた摺動構造を提案する必要があった。   However, as engine parts, for example, automobile engine parts have recently been remarkably improved in performance due to high output and high rotation. Along with this, in a sliding member used in an engine, the performance improvement is limited only by applying the hard carbon coating on the sliding surface. Therefore, it is necessary to propose a sliding structure with more excellent sliding characteristics in consideration of the optimum combination of the sliding member and the lubricating oil.

その一例として、表面にDLCが被覆された摺動部材と、該摺動部材の表面に供給される、植物油、動物油、又は合成油などのベースオイルに有機モリブデン化合物を添加した潤滑油と、を備えた摺動構造が提案されている(例えば特許文献1参照)。本発明によれば、添加剤である有機モリブデン化合物が摺動時に固体潤滑剤として作用することにより、摺動部材の摩擦の低減、及び、耐摩耗性の向上を図ることができる。   For example, a sliding member whose surface is coated with DLC, and a lubricating oil in which an organic molybdenum compound is added to a base oil such as vegetable oil, animal oil, or synthetic oil supplied to the surface of the sliding member. A sliding structure has been proposed (see, for example, Patent Document 1). According to the present invention, since the organic molybdenum compound as an additive acts as a solid lubricant during sliding, the friction of the sliding member can be reduced and the wear resistance can be improved.

特開平2004−339486号公報Japanese Patent Laid-Open No. 2004-339486

これまでの研究において、硬質炭素被膜が形成された摺動部材に供給する潤滑油に、特許文献1に示すベース油のみを用いた場合には、前記硬質炭素被膜の低摩擦特性が充分得られないとされており、特許文献1に記載摺動構造の如く、潤滑油に添加剤を添加することにより摺動特性を図ることが一般的であった。   In the past research, when only the base oil shown in Patent Document 1 is used as the lubricating oil supplied to the sliding member on which the hard carbon film is formed, the low friction characteristic of the hard carbon film is sufficiently obtained. In general, the sliding characteristic is improved by adding an additive to the lubricating oil as in the sliding structure described in Patent Document 1.

しかし、前記添加剤を加えた潤滑油を用いた場合であっても、せいぜい摩擦係数は0.1程度しか期待できず、前述したエンジン等の厳しい摺動環境下では、摺動面間が高面圧となるため、その摺動特性が充分なものであるとは言い難い場合があった。また、前記潤滑剤は、効果が発揮できる適量の添加剤を潤滑剤に配合し調整せねばならず、添加剤の種類及び量が増加するに従って潤滑油のコストも増加する。さらに、潤滑油に添加される金属元素の多くは重金属であり、環境保全をベースとした開発等が盛んな今日の趨勢を鑑みた場合、前記金属元素等を含む添加剤を潤滑油に添加しないほうがより好ましいといえる。   However, even when the lubricating oil added with the additive is used, the friction coefficient can only be expected to be about 0.1 at most, and the sliding surface is high in the severe sliding environment such as the engine described above. Because of the contact pressure, it may be difficult to say that the sliding characteristics are sufficient. In addition, the lubricant must be adjusted by adding an appropriate amount of additive capable of exhibiting the effect to the lubricant, and the cost of the lubricating oil increases as the type and amount of the additive increase. Furthermore, most of the metal elements added to the lubricating oil are heavy metals. In view of the current trend of development based on environmental conservation, the additives containing the metal elements and the like are not added to the lubricating oil. It can be said that it is more preferable.

本発明は、上記する問題に鑑みてなされたものであり、その目的とするところは、耐環境性を考慮しつつコストの低減を図ると共に、たとえ、高面圧等の厳しい摺動環境下であっても、摩擦係数を低減しかつ耐摩耗性を向上させることができる摺動構造を提供することにある。   The present invention has been made in view of the above-mentioned problems, and its object is to reduce costs while considering environmental resistance, and even under severe sliding environments such as high surface pressure. Even if it exists, it is providing the sliding structure which can reduce a friction coefficient and can improve abrasion resistance.

前記課題を鑑み、発明者らは、鋭意検討を重ねた結果、耐環境性及びコスト低減を考慮した場合には、植物油(植物性潤滑油)を用いることが好適であると考えた。そして、潤滑油として様々な植物油を用いて実験を行った結果、特定の植物油に含まれる特定成分が潤滑油に含有することにより、金属添加剤等を添加することなく、画期的に、摩擦係数を低減させることができ、かつ、耐摩耗性を向上させることができるとの新たな知見を得た。   In view of the above problems, the inventors have intensively studied and have considered that it is preferable to use vegetable oil (vegetable lubricating oil) when considering environmental resistance and cost reduction. And as a result of conducting experiments using various vegetable oils as lubricating oils, the specific components contained in the specific vegetable oils contained in the lubricating oils, and, without adding metal additives etc. A new finding has been obtained that the coefficient can be reduced and the wear resistance can be improved.

本発明は、前記新たな知見に基づくものであり、本発明に係る摺動構造は、相互に摺動する摺動面のうち少なくとも一方の摺動面に硬質炭素被膜が形成された一対の摺動部材と、該一対の摺動部材の間に存在する潤滑油と、を備えた摺動構造であって、前記潤滑油は、オレイン酸、リノール酸、及びリノレン酸のうち少なくとも1種を含む植物性潤滑油であることを特徴とする。   The present invention is based on the above-mentioned new knowledge, and the sliding structure according to the present invention includes a pair of slides in which a hard carbon coating is formed on at least one of the sliding surfaces sliding relative to each other. A sliding structure comprising a moving member and a lubricating oil present between the pair of sliding members, wherein the lubricating oil includes at least one of oleic acid, linoleic acid, and linolenic acid. It is a vegetable lubricating oil.

本発明に係る摺動構造は、互いに摺動する1対の摺動部材の少なくとも一方の摺動面に、硬質炭素被膜が形成されている。さらに、硬質炭素被膜が形成された摺動部材の摺動面と、該摺動面に摺動する摺動部材の摺動面との間には、潤滑油が存在する構成となっている。本発明にいう「相互に摺動する」とは、少なくとも一方の摺動部材が他方の摺動部材に対して相対的に摺動することをいい、相対的な摺動とは、直線運動、回転運動、又はこれらの運動の組み合わせにより摺動することをいう。   In the sliding structure according to the present invention, a hard carbon coating is formed on at least one sliding surface of a pair of sliding members that slide relative to each other. Furthermore, the lubricating oil exists between the sliding surface of the sliding member on which the hard carbon film is formed and the sliding surface of the sliding member that slides on the sliding surface. In the present invention, “sliding relative to each other” means that at least one sliding member slides relative to the other sliding member, and relative sliding refers to linear motion, Sliding by rotational movement or a combination of these movements.

そして、発明者らの後述する実験からも明らかなように、前記潤滑油として、オレイン酸、リノール酸、及びリノレン酸の不飽和脂肪酸うち少なくとも1種の不飽和脂肪酸を含む植物性潤滑油を用いることにより、硬質炭素被膜が形成された摺動部材の摩擦係数を低減すると共に耐摩耗性を向上させることができる。オレイン酸、リノール酸、又はリノレン酸は、不飽和の分子構造であり、かつ極性をもった分子構造であり、該分子構造が、摩擦係数の低減及び耐摩耗性を向上させる一因になると考えられる。また、植物性潤滑油、すなわち植物油を潤滑油に用いることにより、環境にやさしく、さらには、これらの植物油は安価に入手し易く経済的である。   As is apparent from the experiments described later by the inventors, a vegetable lubricating oil containing at least one unsaturated fatty acid among the unsaturated fatty acids of oleic acid, linoleic acid, and linolenic acid is used as the lubricating oil. As a result, the friction coefficient of the sliding member on which the hard carbon film is formed can be reduced and the wear resistance can be improved. Oleic acid, linoleic acid, or linolenic acid has an unsaturated molecular structure and a polar molecular structure, and this molecular structure is considered to contribute to a reduction in friction coefficient and an improvement in wear resistance. It is done. Further, by using vegetable lubricating oil, that is, vegetable oil, as the lubricating oil, it is environmentally friendly. Furthermore, these vegetable oils are easily available at low cost and are economical.

植物性潤滑油としては、オリーブ油、カカオ油、ゴマ油、大豆油、とうもろこし油、ナタネ油、パーム油、ひまわり油、サフラワー油、こむぎ胚芽油、やし油、落花生油、またはアマニ油等を挙げることができ、これらの植物油を混合した混合油であってもよい。また、より好ましくは、これらの不飽和脂肪酸のうち少なくとも一種を主剤として含む、後述するオリーブ油、サフラワー油、アマニ油等である。   Examples of vegetable lubricating oils include olive oil, cacao oil, sesame oil, soybean oil, corn oil, rapeseed oil, palm oil, sunflower oil, safflower oil, wheat germ oil, palm oil, peanut oil, or linseed oil It may be a mixed oil obtained by mixing these vegetable oils. More preferred are olive oil, safflower oil, linseed oil, etc., which will be described later, containing at least one of these unsaturated fatty acids as a main ingredient.

本発明に係る摺動構造は、前記硬質炭素被膜として、例えばダイヤモンド被膜などの炭素が結晶化した被膜、非晶質炭素被膜などのアモルファス構造を含む被膜など、被膜を被覆する基材に比べて硬質な炭素被膜であれば得に限定されるものではない。しかし、より好ましい硬質炭素被膜は、非晶質炭素被膜(Diamond Like Carbon からなる被膜:DLC被膜)又は窒化炭素被膜(CNx被膜)である。また、窒化炭素被膜のうち非晶質窒化炭素被膜がより好ましい。該被膜は、非晶質炭素被膜に比べて、摺動面となる表面がより活性であるため、摺動時に、より強固な境界潤滑膜を形成することができると考えられる。この結果、非晶質炭素被膜に比べてさらに低い摩擦係数を得ることができる。   The sliding structure according to the present invention has a hard carbon coating as compared with a base material on which the coating is applied, such as a coating obtained by crystallizing carbon such as a diamond coating or a coating containing an amorphous structure such as an amorphous carbon coating. If it is a hard carbon film, it will not be limited to gain. However, a more preferable hard carbon coating is an amorphous carbon coating (a coating made of Diamond Like Carbon: a DLC coating) or a carbon nitride coating (CNx coating). Moreover, an amorphous carbon nitride film is more preferable among the carbon nitride films. Since the surface of the coating is more active than the amorphous carbon coating, it is considered that a stronger boundary lubricating film can be formed during sliding. As a result, a lower friction coefficient can be obtained as compared with the amorphous carbon coating.

前記に示した硬質炭素被膜を摺動部材の基材表面に成膜するにあたっては、真空蒸着、スパッタリング、イオンプレーティング、イオンビームミキシングなどを利用した物理気相成長法(PVD)により成膜してもよく、プラズマ処理などを利用した化学気相成長法(CVD)により成膜してもよく、これらの方法を組み合わせた方法により成膜してもよい。また、DLC被膜の一種である非晶質窒化炭素被膜を成膜する場合、窒化炭素被膜(CNx被膜)を成膜する場合には、より安定した低摩擦特性を得るために、被膜形成とイオン注入とを同時に行うダイナミクスミキシング法によるイオンビーム法により、これら被膜を形成することがより好ましい。また、このような成膜時において硬質炭素被膜中に、Si、Ti、Cr、Fe、Mo、W、Bなどの添加元素を含有させてもよく、このような元素を添加することにより、被膜の表面硬さを調整することもできる。   When forming the hard carbon film described above on the surface of the base material of the sliding member, the film is formed by physical vapor deposition (PVD) using vacuum deposition, sputtering, ion plating, ion beam mixing, or the like. Alternatively, the film may be formed by chemical vapor deposition (CVD) utilizing plasma treatment or the like, or may be formed by a combination of these methods. In addition, when forming an amorphous carbon nitride film, which is a kind of DLC film, when forming a carbon nitride film (CNx film), in order to obtain more stable low friction characteristics, film formation and ion It is more preferable to form these films by an ion beam method based on a dynamic mixing method in which the implantation is performed simultaneously. Further, during such film formation, an additive element such as Si, Ti, Cr, Fe, Mo, W, or B may be included in the hard carbon film, and by adding such an element, the film The surface hardness can be adjusted.

さらに、硬質炭素被膜を摺動部材の表面に成膜するにあたっては、摺動部材の基材とこの被膜との間の密着力を高めるために、ケイ素(Si)からなる中間層を設けてもよく、さらにケイ素の代わりに、クロム(Cr)、チタン(Ti)またはタングステン(W)を用いてもよい。   Further, when forming the hard carbon film on the surface of the sliding member, an intermediate layer made of silicon (Si) may be provided in order to increase the adhesion between the base material of the sliding member and this film. Further, chromium (Cr), titanium (Ti), or tungsten (W) may be used instead of silicon.

さらに、この硬質炭素被膜を表面に成膜する基材は、摺動時において硬質炭素被膜との密着性を確保することができるような材質および表面硬さであれば、鉄、非鉄金属等と特に限定されるものではなく、この摺動部材と摺動する他方の摺動部材も、この硬質炭素被膜に対して極端に表面硬さが低く、摺動時に摩耗し易いものでなければ、その材質は特に限定されるものではない。   Furthermore, if the base material on which the hard carbon film is formed has a material and surface hardness that can ensure adhesion to the hard carbon film during sliding, iron, non-ferrous metal, etc. There is no particular limitation, and the other sliding member that slides with this sliding member is also extremely low in surface hardness with respect to this hard carbon coating and is not easily worn when sliding. The material is not particularly limited.

また、本発明に係る摺動構造は、前記潤滑油が、オレイン酸を少なくとも含んでおり、該オレイン酸は、前記潤滑油に対して70〜85質量%含むことがより好ましい。本発明によれば、前記範囲の含有率となるようにオレイン酸を含むことにより、一対の摺動部材の摩擦係数を低減させることができ、かつ、これらの耐摩耗性を向上させることができる。前記範囲よりも少ない場合には、摩擦係数が高くなる等、より好適な摺動特性を得ることができないことがあり、前記範囲よりも多いであってもそれ以上の効果は期待できない。また、この範囲よりも多いオレイン酸を天然の植物油から得ることは難しく、製油等により製造した場合にはコストが高くなるおそれがある。なお、前記範囲含有率のオレイン酸を含む好適な植物油として例えばオリーブ油が挙げられる。   Moreover, as for the sliding structure which concerns on this invention, the said lubricating oil contains at least oleic acid, and it is more preferable that this oleic acid contains 70-85 mass% with respect to the said lubricating oil. According to the present invention, by containing oleic acid so as to have a content in the above range, the friction coefficient of the pair of sliding members can be reduced, and the wear resistance can be improved. . If the amount is less than the above range, a more favorable sliding characteristic may not be obtained, for example, the friction coefficient becomes high. Even if the amount is more than the above range, no further effect can be expected. Moreover, it is difficult to obtain more oleic acid than this range from natural vegetable oil, and when manufactured by oil production etc., there exists a possibility that cost may become high. In addition, olive oil is mentioned as a suitable vegetable oil containing the oleic acid of the said range content rate, for example.

また、別の態様としては、本発明に係る摺動構造は、前記潤滑油が、リノール酸を少なくとも含んでおり、該リノール酸は、前記潤滑油に対して60〜80質量%含むことがより好ましい。本発明によれば、前記範囲の含有率となるように、リノール酸を含むことにより、一対の摺動部材の摩擦係数を低減させることができ、かつ、これらの耐摩耗性を向上させることができる。なお、リノール酸は、前記オレイン酸よりも不飽和度が大きいため、前記オレイン酸の含有率よりも低い。また、前記範囲よりも少ない場合には、摩擦係数が高くなる等、より好適な摺動特性を得ることができないことがあり、前記範囲よりも多いであってもそれ以上の効果は期待できない。さらに、この範囲よりも多いリノール酸を天然の植物油から得ることは難しく、製油等により製造した場合にはコストが高くなるおそれがある。なお、前記範囲含有率のリノールを含む好適な植物油として例えばひまわり油、サフラワー油、または、こむぎ胚芽油等が挙げられる。   As another aspect, in the sliding structure according to the present invention, the lubricating oil contains at least linoleic acid, and the linoleic acid may contain 60 to 80% by mass with respect to the lubricating oil. preferable. According to the present invention, by including linoleic acid so that the content ratio is in the above range, the friction coefficient of the pair of sliding members can be reduced, and the wear resistance can be improved. it can. In addition, since linoleic acid has a higher degree of unsaturation than the oleic acid, it is lower than the content of the oleic acid. Further, if the amount is less than the above range, a more favorable sliding characteristic may not be obtained, for example, the friction coefficient becomes high. Even if the amount is more than the above range, no further effect can be expected. Furthermore, it is difficult to obtain more linoleic acid than this range from natural vegetable oil, and the cost may increase when it is produced by oil production or the like. In addition, as a suitable vegetable oil containing linole of the said range content rate, a sunflower oil, safflower oil, or a wheat germ oil etc. are mentioned, for example.

さらに、別の態様としては、本発明に係る摺動構造は、前記潤滑油が、リノレン酸を少なくとも含んでおり、該リノレン酸は、前記潤滑油に対して30〜60質量%含むことがより好ましい。本発明によれば、前記範囲の含有率となるように、リノレン酸を含むことにより、一対の摺動部材の摩擦係数を低減させることができ、かつ、これらの耐摩耗性を向上させることができる。なお、リノレン酸は、前記リノール酸よりも不飽和度が大きいため、前記リノール酸の含有率よりも低い。また、前記範囲よりも少ない場合には、摩擦係数が高くなる等、より好適な摺動特性を得ることができないことがあり、前記範囲よりも多いであってもそれ以上の効果は期待できない。さらに、この範囲よりも多いリノレン酸を天然の植物油から得ることは難しい。なお、前記範囲含有率のリノレン酸を含む好適な植物油として例えばアマニ油が挙げられる。   Furthermore, as another aspect, in the sliding structure according to the present invention, the lubricating oil may contain at least linolenic acid, and the linolenic acid may contain 30 to 60% by mass with respect to the lubricating oil. preferable. According to the present invention, by including linolenic acid so as to have a content in the above range, the friction coefficient of the pair of sliding members can be reduced, and the wear resistance can be improved. it can. Since linolenic acid has a higher degree of unsaturation than linoleic acid, it is lower than the content of linoleic acid. Further, if the amount is less than the above range, a more favorable sliding characteristic may not be obtained, for example, the friction coefficient becomes high. Even if the amount is more than the above range, no further effect can be expected. Furthermore, it is difficult to obtain more linolenic acid from this range from natural vegetable oils. An example of a suitable vegetable oil containing linolenic acid in the above range is linseed oil.

また、本発明に係る摺動構造は、一対の摺動部材同士の間に安定的に潤滑油を存在させるために、潤滑油を摺動部材に配置させる(供給する)機構として、循環潤滑機構、ミスト潤滑機構、又は、オイルバスによる油浴潤滑機構などをさらに設けてもよく、摺動時に摺動部材間に、潤滑油が安定的に給油されるのであれば、その機構は特に限定されるものではない。さらに、前記潤滑油には、酸化防止剤、摩耗防止剤、極圧剤、摩擦調整剤、金属不活性剤、清浄剤、防錆剤、泡消剤などを適宜添加することも可能である。   Further, the sliding structure according to the present invention has a circulating lubrication mechanism as a mechanism for arranging (supplying) the lubricating oil on the sliding member in order to allow the lubricating oil to stably exist between the pair of sliding members. In addition, a mist lubrication mechanism or an oil bath lubrication mechanism using an oil bath may be further provided, and the mechanism is particularly limited as long as the lubricating oil is stably supplied between the sliding members during sliding. It is not something. Furthermore, an antioxidant, an antiwear agent, an extreme pressure agent, a friction modifier, a metal deactivator, a detergent, a rust inhibitor, an antifoaming agent, and the like can be added as appropriate to the lubricating oil.

本発明に係る摺動構造によれば、耐環境性を考慮しつつコストの低減を図ると共に、たとえ、高面圧等の厳しい摺動環境下であっても、摩擦係数を低減しかつ耐摩耗性を向上させることができる。   According to the sliding structure of the present invention, the cost is reduced while considering the environmental resistance, and the friction coefficient is reduced and the wear resistance is reduced even in a severe sliding environment such as a high surface pressure. Can be improved.

以下に、本発明を実施例により説明する。なお、本発明は、以下に示す実施例に限定されるものではない。   Hereinafter, the present invention will be described by way of examples. In addition, this invention is not limited to the Example shown below.

(実施例1−1)
本発明に係る摺動構造の一対の摺動部材のうち、硬質炭素被膜を形成した一方の摺動部材として以下に示すディスク試験片を製作し、この摺動部材と摺動する他方の摺動部材として、以下に示すボール試験片を製作した。
(Example 1-1)
Of the pair of sliding members of the sliding structure according to the present invention, the following disk test piece is manufactured as one sliding member on which a hard carbon film is formed, and the other sliding member sliding with this sliding member As a member, the following ball test piece was manufactured.

<ディスク試験片>
硬質炭素被膜を成膜する基材として、直径50mm、厚み0.3mm、円部表面(摺動面)が鏡面状態(100面方位)となる、ディスク形状のシリコンウェハSを準備した。そして、図1に示すようなイオンビームミキシング装置10(日立製作所製 1X−30−30)を用いて、このシリコンウェハSの円部表面に非晶質の窒化炭素(CNx)被膜(硬質炭素被膜)を成膜した。なお、イオンビームミキシング法は、基材と薄膜(表面改質層)との間にミキシング層が形成されるため、従来の基材/被膜境界がなく、被膜との密着性や、被膜の組成制御性に優れた表面処理が可能な成膜方法である。
<Disk specimen>
A disk-shaped silicon wafer S having a diameter of 50 mm, a thickness of 0.3 mm, and a circular surface (sliding surface) in a mirror surface state (100 plane orientation) was prepared as a base material on which a hard carbon film was formed. Then, using an ion beam mixing apparatus 10 (1X-30-30, manufactured by Hitachi, Ltd.) as shown in FIG. 1, an amorphous carbon nitride (CNx) film (hard carbon film) is formed on the surface of the circular portion of the silicon wafer S. ) Was formed. In the ion beam mixing method, since the mixing layer is formed between the substrate and the thin film (surface modified layer), there is no conventional substrate / film boundary, adhesion to the film, and composition of the film. This is a film forming method capable of surface treatment with excellent controllability.

図1に示すように、イオンビームミキシング装置10は、真空チャンバ11、基板ホルダ12、アシスト用イオン源及びガス供給源14、スパッタイオン源15、クライオポンプ16を少なくとも備えており、イオン源はスパッタ用、アシスト用、共にバケット型であり、スパッタイオン源は加速電圧最大1500eV、イオン電流最大200mA、イオンビーム有効径は直径約80mmである。基板ホルダ12は成膜中回転し、またイオンビームと基板表面との角度を0°〜90°の範囲で変化させることができるように構成されている。このような装置10を用いて、以下のように成膜した。   As shown in FIG. 1, the ion beam mixing apparatus 10 includes at least a vacuum chamber 11, a substrate holder 12, an assisting ion source and gas supply source 14, a sputter ion source 15, and a cryopump 16. The ion source is a sputter. Both of the ion source and the assist type are bucket types, the sputter ion source has an acceleration voltage of 1500 eV at the maximum, an ion current of 200 mA at the maximum, and an effective diameter of the ion beam of about 80 mm. The substrate holder 12 is configured to rotate during film formation and to change the angle between the ion beam and the substrate surface within a range of 0 ° to 90 °. Using such an apparatus 10, a film was formed as follows.

具体的には、図1に示すように、シリコンウェハSの円部表面が支持台13上に配置された純度99.9999%のカーボンターゲットTと対向するように、真空チャンバ11内のホルダ12にシリコンウェハSを取り付けた。その後、真空チャンバ11内の圧力を、クライオポンプ16で、2.0×10−4Pa以下に減圧調整し、窒素イオンgn(加速電圧1keV,イオン電流密度μA/cm)を5分間シリコンウェハSに向けて照射して、スパッタクリーニングした。その後、真空チャンバ11内の圧力を、1.4×10−2Paに調整し、スパッタイオン源15からアルゴンイオンgaをカーボンターゲットTに照射し、カーボンターゲットTをカーボンスパッター粒子scにすると同時に、ホルダ12と共にシリコンウェハSを4rpmに回転させ、シリコンウェハの円部表面に厚さ100nmの非晶質の窒化炭素被膜(CNx被膜)を成膜した。 Specifically, as shown in FIG. 1, the holder 12 in the vacuum chamber 11 is arranged so that the circular surface of the silicon wafer S faces the carbon target T with a purity of 99.9999% arranged on the support base 13. A silicon wafer S was attached to the substrate. Thereafter, the pressure in the vacuum chamber 11 is adjusted to 2.0 × 10 −4 Pa or less with a cryopump 16, and nitrogen ions gn (acceleration voltage 1 keV, ion current density μA / cm 2 ) is applied to the silicon wafer for 5 minutes. Irradiation toward S and sputter cleaning was performed. Thereafter, the pressure in the vacuum chamber 11 is adjusted to 1.4 × 10 −2 Pa, and the carbon target T is irradiated with argon ions ga from the sputter ion source 15 to convert the carbon target T into carbon sputtered particles sc. The silicon wafer S was rotated at 4 rpm together with the holder 12, and an amorphous carbon nitride film (CNx film) having a thickness of 100 nm was formed on the circular surface of the silicon wafer.

<ボール試験片>
直径8mm、以下の表1に示す窒化珪素球を準備し、該球の表面に同じようにして、窒化炭素被膜を200nm成膜した。
<Ball specimen>
A silicon nitride sphere having a diameter of 8 mm and shown in Table 1 below was prepared, and a carbon nitride film was formed in a thickness of 200 nm on the surface of the sphere in the same manner.

<潤滑油>
植物性潤滑油でグリセリンにリノール酸及びオレイン酸の不飽和脂肪酸が付いた構造であるアシルグリセロールを準備した。この植物性潤滑油は、ナタネ油と大豆油から得ることができる潤滑油である。
<Lubricating oil>
Acylglycerol, which is a structure obtained by adding linoleic acid and unsaturated fatty acid of oleic acid to glycerin with vegetable lubricating oil, was prepared. This vegetable lubricating oil is a lubricating oil that can be obtained from rapeseed oil and soybean oil.

Figure 2009013370
Figure 2009013370

<摩耗試験>
図2に示すピンオンディスク摩擦試験機30を用いた。尚、本発明に係る「一対の摺動部材」はディスク試験片とボール試験片を示している。
<Abrasion test>
A pin-on-disk friction tester 30 shown in FIG. 2 was used. The “pair of sliding members” according to the present invention indicates a disk test piece and a ball test piece.

摩耗試験を行う事前準備として、ボール試験片Bをアセトンとエタノールで各10分間超音波洗浄した。その後、ボール試験片Bを試験機の本体から取り外し、ボールホルダー31に固定し、光学顕微鏡(図示せず)を用いて表面に傷が無いことを確認後、これらをデシケータ(図示せず)内に投入し、ボール試験片Bを乾燥させた。一方、ディスク試験片Dの表面に形成したCNx被膜の表面(摺動面)の埃などの異物をハンドブロー(図示せず)で取り除いた。   As a preliminary preparation for the wear test, the ball specimen B was ultrasonically cleaned with acetone and ethanol for 10 minutes each. Thereafter, the ball test piece B is removed from the main body of the testing machine, fixed to the ball holder 31, and after confirming that there is no scratch on the surface using an optical microscope (not shown), these are placed in a desiccator (not shown). The ball test piece B was dried. On the other hand, foreign matters such as dust on the surface (sliding surface) of the CNx film formed on the surface of the disk test piece D were removed by hand blow (not shown).

次に、ディスク試験片Dをディスクホルダー32に保持させると共に、ボール試験片Bが固定されたボールホルダー31をステージ33と一体となるように試験機の本体に取り付けた。そして、試験時にディスク試験片Dの表面に潤滑油Lが常時存在するように、ホルダー32に潤滑油が1mmの高さになるまで供給した。さらに、平行板ばね34に接着したひずみゲージ34(協和電業製,KF−1−120−C1−16)を用いて、ボール試験片Bがディスク試験片DのCNx被膜の表面に対して付加される荷重の値が1.0Nとなるようにステージ33を調整して、ディスク試験片Dにボール試験片Bを押付けた。   Next, the disc test piece D was held by the disc holder 32, and the ball holder 31 to which the ball test piece B was fixed was attached to the main body of the testing machine so as to be integrated with the stage 33. Then, the lubricating oil was supplied to the holder 32 until the height reached 1 mm so that the lubricating oil L was always present on the surface of the disk test piece D during the test. Further, a ball test piece B is added to the surface of the CNx coating of the disk test piece D using a strain gauge 34 (Kyowa Dengyo Co., Ltd., KF-1-120-C1-16) bonded to the parallel leaf spring 34. The stage 33 was adjusted so that the value of the applied load was 1.0 N, and the ball test piece B was pressed against the disk test piece D.

この押付け状態を保持して、モータ37を駆動して、カップリング38を介してディスクホルダー32のディスク試験片Dを、摺動速度1.26×10−2m/sとなるように回転させ、このときの摩擦力を、ひずみゲージ34で測定し、センサインターフェイス(協和電業製,PCD−300A)を介して、コンピュータ内にデータを取り込み、記録した。そして、摩擦係数を換算した。この結果を図3に示す。 Holding this pressed state, the motor 37 is driven to rotate the disk test piece D of the disk holder 32 through the coupling 38 so that the sliding speed is 1.26 × 10 −2 m / s. The frictional force at this time was measured with a strain gauge 34, and data was taken into a computer and recorded via a sensor interface (PCD-300A, manufactured by Kyowa Dengyo). And the friction coefficient was converted. The result is shown in FIG.

(実施例1−2)
実施例1−1と同じように、ディスク試験片D、ボール試験片B、潤滑油Lを準備した。実施例1−1と相違する点は、ディスク試験片Dの表面に、プラズマCVDにより、DLC被膜(HT−DLC(厚膜、高信頼性DLC:日本アイ・ティ・エフ株式会社製)を成膜した点である。そして、実施例1−1と同様の摩擦試験条件で摩擦係数を測定した。この結果を図3に示す。
(Example 1-2)
As in Example 1-1, a disk test piece D, a ball test piece B, and a lubricating oil L were prepared. The difference from Example 1-1 is that a DLC film (HT-DLC (thick film, highly reliable DLC: manufactured by Japan IT Corporation)) is formed on the surface of the disk specimen D by plasma CVD. The friction coefficient was measured under the same friction test conditions as in Example 1-1, and the results are shown in FIG.

(比較例1−1〜7−1)
実施例1−1と同じように、ディスク試験片D、ボール試験片B、潤滑油Lを準備した。実施例1−1と相違する点は、潤滑油であり、比較例1−1〜7−1は、潤滑油の代わりに、順次、鉱物油であるベースオイル5W−30、純水、エタノール(COH)、ケロシン(灯油)、シリコン油、ホルムアルデヒド(HCONH:ギ酸のアミド)、ヘキサン(C14)を用いた点である。そして、実施例1−1と同様の摩擦試験条件で摩擦係数を測定した。この結果を図3に示す。
(Comparative Examples 1-1 to 7-1)
As in Example 1-1, a disk test piece D, a ball test piece B, and a lubricating oil L were prepared. The difference from Example 1-1 is a lubricating oil, and Comparative Examples 1-1 to 7-1 are, in place of the lubricating oil, base oil 5W-30, which is a mineral oil, pure water, ethanol (C 2 H 5 OH), kerosene (kerosene), silicon oil, formaldehyde (HCONH 2 : amide of formic acid), and hexane (C 6 H 14 ). And the friction coefficient was measured on the friction test conditions similar to Example 1-1. The result is shown in FIG.

(比較例1−2〜7−2)
実施例1−2と同じように、ディスク試験片D、ボール試験片B、潤滑油Lを準備した。実施例1−2と相違する点は、潤滑油であり、比較例1−2〜7−2の供給する潤滑油等は、順次比較例1−1〜7−1の潤滑油等に対応している。そして、実施例1−2と同様の摩擦試験条件で摩擦係数を測定した。この結果を図3に示す。
(Comparative Examples 1-2 to 7-2)
As in Example 1-2, a disk test piece D, a ball test piece B, and a lubricating oil L were prepared. The difference from Example 1-2 is the lubricating oil, and the lubricating oil supplied in Comparative Examples 1-2 to 7-2 corresponds to the lubricating oil in Comparative Examples 1-1 to 7-1 in order. ing. And the friction coefficient was measured on the friction test conditions similar to Example 1-2. The result is shown in FIG.

(結果1及び考察1)
この試験結果から、CNx被膜を用いて得られる摩擦係数のほうが、DLC被膜を用いて得られる摩擦係数よりも低い傾向があることが確認された。これはCNx膜の方が、DLC被膜よりも活性が高く、より強固な境界潤滑膜が摺動時に形成されたためであると考えられる。なお、比較例4のケロシン、比較例7のヘキサンを潤滑させた場合に、CNx被膜を用いて得られる摩擦係数がDLC被膜を用いて得られるものよりも高いのは、ケロシン、ヘキサンが他のものに比べてせん断抵抗が大きいからである。
(Result 1 and Discussion 1)
From this test result, it was confirmed that the friction coefficient obtained using the CNx film tends to be lower than the friction coefficient obtained using the DLC film. This is considered to be because the CNx film has higher activity than the DLC film, and a stronger boundary lubricating film was formed during sliding. When the kerosene of Comparative Example 4 and the hexane of Comparative Example 7 are lubricated, the friction coefficient obtained using the CNx coating is higher than that obtained using the DLC coating. This is because the shear resistance is larger than that.

また、実施例1−1,1−2の植物性潤滑油下においては、CNx膜、DLC膜ともに低い摩擦係数が得られた。これは、実施例1−1,1−2の植物性潤滑油は、リノール酸、オレイン酸などの不飽和の分子や、極性をもった分子が、他のものに比べて多く存在しているからであると考えられる。   Moreover, under the vegetable lubricating oil of Examples 1-1 and 1-2, a low friction coefficient was obtained for both the CNx film and the DLC film. This is because the vegetable lubricating oils of Examples 1-1 and 1-2 have a lot of unsaturated molecules such as linoleic acid and oleic acid, and molecules having polarity compared to others. It is thought that it is from.

(実施例2〜4)
実施例1−1と同じように、ディスク試験片D、ボール試験片B、潤滑油Lを準備した。実施例1−1と相違する点は、潤滑油であり、実施例2〜4の供給する潤滑油を、オレイン酸、リノール酸、リノレン酸にした点である。そして、実施例1−1と同様の摩擦試験条件で摩擦係数を測定した。実施例1−1と相違する条件は、摺動速度を3.14×10−2m/sにした点である。この結果を図4に示す。また、試験終了後、各ディスク試験片Dを試験機30から取り出して、原子間力顕微鏡(AFM)を用いて、CNx被膜に形成された摩耗痕の断面積を求めて、この被膜の比摩耗量を算出した。この結果を、図5に示す。
(Examples 2 to 4)
As in Example 1-1, a disk test piece D, a ball test piece B, and a lubricating oil L were prepared. The difference from Example 1-1 is a lubricating oil, and the lubricating oil supplied in Examples 2 to 4 is changed to oleic acid, linoleic acid, and linolenic acid. And the friction coefficient was measured on the friction test conditions similar to Example 1-1. The condition different from that of Example 1-1 is that the sliding speed is set to 3.14 × 10 −2 m / s. The result is shown in FIG. Further, after the test is completed, each disk specimen D is taken out from the testing machine 30 and the cross-sectional area of the wear mark formed on the CNx film is obtained using an atomic force microscope (AFM), and the specific wear of this film is determined. The amount was calculated. The result is shown in FIG.

(比較例8)
比較例1−1と同じように、ディスク試験片D、ボール試験片B、潤滑油(ベースオイル)Lを準備した。そして、実施例2と同じように、摩擦係数及び比摩耗量を測定した。この結果を図4及び図5に示す。
(Comparative Example 8)
As in Comparative Example 1-1, a disk specimen D, a ball specimen B, and a lubricating oil (base oil) L were prepared. In the same manner as in Example 2, the friction coefficient and the specific wear amount were measured. The results are shown in FIGS.

(結果2及び考察2)
図4、5に示すように、実施例2〜4の摩擦係数が、比較例8ものに比べて、略1/3程度となり、さらに、実施例2〜4の比摩耗量は、1/20程度となった。実施例2〜4のオレイン酸、リノール酸、リノレン酸の順で不飽和度(炭素数に対する2重結合の数)は高まっており、いずれの不飽和脂肪酸であっても、摩擦係数は平均0.024〜0.035程度であった。但し、実施例2、3の比摩耗量の結果からも明らかなように、オレイン酸、リノール酸のように、不飽和度の小さい脂肪酸では、摩擦係数が他のものに比べてさらに小さかった。この結果から、不飽和度の低いものほど、摩擦係数が小さい傾向にあると考えられる。また同様に、比摩耗量の結果からしても、不飽和度の低いものほど、摩擦係数が小さい傾向にあると考えられる。
(Result 2 and discussion 2)
As shown in FIGS. 4 and 5, the friction coefficients of Examples 2 to 4 are about 1/3 of those of Comparative Example 8, and the specific wear amount of Examples 2 to 4 is 1/20. It became about. The degree of unsaturation (number of double bonds with respect to the number of carbon atoms) increased in the order of oleic acid, linoleic acid, and linolenic acid in Examples 2 to 4, and the friction coefficient averaged 0 for any unsaturated fatty acid. It was about .024 to 0.035. However, as is clear from the results of specific wear amounts of Examples 2 and 3, the fatty acid having a low degree of unsaturation such as oleic acid and linoleic acid had a smaller friction coefficient than that of the other. From this result, it is considered that the lower the degree of unsaturation, the smaller the friction coefficient tends to be. Similarly, from the result of the specific wear amount, it is considered that the lower the degree of unsaturation, the smaller the coefficient of friction.

(実施例5〜7)
実施例4と同じように、ディスク試験片D、ボール試験片B、潤滑油Lを準備した。実施例4と相違する点は、潤滑油である。
(Examples 5-7)
As in Example 4, a disk specimen D, a ball specimen B, and a lubricating oil L were prepared. The difference from the fourth embodiment is the lubricating oil.

具体的には、実施例5は、オレイン酸を70〜85質量%含む潤滑油としてオリーブ油を使用した。具体的には、このオリーブ油は、オレイン酸(80質量%)、パルチミン酸(10質量%)、残り他の脂肪酸(例えば飽和脂肪酸)を含んでいる潤滑油である。実施例6は、リノール酸を60〜80質量%含む潤滑油としてサフラワー油を使用した。具体的には、このサフラワー油は、リノール酸(60質量%)、オレイン酸(20質量%)、パルチミン酸(10質量%)、及び残り他の脂肪酸(例えば飽和脂肪酸)を含んでいる潤滑油である。実施例7は、リノレン酸を30〜60質量%含む潤滑油としてアマニ油を使用した。具体的には、このアマニ油は、リノレン酸(50〜60質量%)、リノール酸(15質量%)、オレイン酸(10質量%)、及び残り他の脂肪酸(例えば飽和脂肪酸)を含んでいる潤滑油である。なお、前述した、オリーブ油、サフラワー油、アマニ油の順で不飽和脂肪酸を含む割合が増加している。   Specifically, Example 5 used olive oil as a lubricating oil containing 70 to 85% by mass of oleic acid. Specifically, this olive oil is a lubricating oil containing oleic acid (80% by mass), palmitic acid (10% by mass), and other remaining fatty acids (for example, saturated fatty acids). In Example 6, safflower oil was used as a lubricating oil containing 60-80% by mass of linoleic acid. Specifically, this safflower oil is a lubricating oil containing linoleic acid (60% by weight), oleic acid (20% by weight), palmitic acid (10% by weight), and the remaining other fatty acids (eg, saturated fatty acids). Oil. In Example 7, linseed oil was used as a lubricating oil containing 30 to 60% by mass of linolenic acid. Specifically, this linseed oil contains linolenic acid (50-60% by weight), linoleic acid (15% by weight), oleic acid (10% by weight), and the remaining other fatty acids (eg, saturated fatty acids). Lubricating oil. In addition, the ratio which contains an unsaturated fatty acid is increasing in order of olive oil, safflower oil, and linseed oil mentioned above.

そして、実施例5〜7についても、実施例4と同じように、摩擦係数及び比摩耗量を測定した。この結果を図6及び図7に示す。   And also about Examples 5-7, similarly to Example 4, the friction coefficient and the specific wear amount were measured. The results are shown in FIGS.

(結果3及び考察3)
図6、7に示すように、実施例5〜7の摩擦係数が、比較例8ものに比べて小さく、特に、オリーブ油とアマニ油においては、摩擦係数が0.017、0.018と、他のものに比べて小さい値となった。また、実施例5〜7に示すように、オリーブ油、サフラワー油、アマニ油の順で不飽和脂肪酸を含む割合が増加するにしたがって、比摩耗量は増加した。
(Result 3 and discussion 3)
As shown in FIGS. 6 and 7, the friction coefficients of Examples 5 to 7 are smaller than those of Comparative Example 8. Particularly, olive oil and linseed oil have friction coefficients of 0.017 and 0.018, and others. It became a small value compared with the one. In addition, as shown in Examples 5 to 7, the specific wear amount increased as the proportion of unsaturated fatty acids increased in the order of olive oil, safflower oil, and linseed oil.

このように実施例5〜7は摩擦係数及び比摩耗量が低減されていることから、不飽和度の大きさが大きくなるに従って、含有させる不飽和脂肪酸の量は少量でもよいと考えられる。そして、オレイン酸、リノール酸、リノレン酸を、天然の植物油から採取するには、それぞれ上記に示した範囲であることが好ましく、さらに、それぞれ不飽和脂肪酸に対して、上記範囲よりも少ない場合には、摩擦係数が高くなる等、より好適な摺動特性を得ることができないことがあり、上記範囲よりも多いであってもそれ以上の効果は期待できない可能性があると考えられる。   Thus, since Examples 5-7 have reduced friction coefficients and specific wear amounts, it is considered that the amount of unsaturated fatty acid to be contained may be small as the degree of unsaturation increases. And, in order to collect oleic acid, linoleic acid, and linolenic acid from natural vegetable oil, it is preferable that the ranges are as shown above, respectively, and further, when each is less than the above range for unsaturated fatty acids. May not be able to obtain a more favorable sliding characteristic such as a higher friction coefficient, and it is considered that no further effect can be expected even if the friction coefficient exceeds the above range.

以上、本発明の実施例を詳述してきたが、具体的な構成はこの実施例に限定されるものではなく、本発明の要旨を逸脱しない範囲における設計変更があっても、それらは本発明に含まれるものである。   As mentioned above, although the embodiment of the present invention has been described in detail, the specific configuration is not limited to this embodiment, and even if there is a design change within a scope not departing from the gist of the present invention, they are not limited to the present invention. Is included.

たとえば、本実施例では、一方の摺動部材の基材としてシリコンウェハに硬質炭素被膜を成膜したが、硬質炭素被膜が摺動時において剥離、亀裂の発生等がないのであれば、鉄等の金属材料に被覆してもよい。また、一対の摺動部材の双方の摺動面に硬質炭素被膜を形成する必要はなく、いずれか一方の摺動面にのみ硬質炭素被膜を成膜してもよい。   For example, in this example, a hard carbon film was formed on a silicon wafer as a base material of one sliding member. However, if the hard carbon film does not peel or crack when sliding, iron, etc. The metal material may be coated. Moreover, it is not necessary to form the hard carbon film on both sliding surfaces of the pair of sliding members, and the hard carbon film may be formed only on one of the sliding surfaces.

実施例に係るイオンミキシングビーム装置を説明するための図。The figure for demonstrating the ion mixing beam apparatus which concerns on an Example. 実施例に係るピンオンディスク摩擦試験機を説明するための図。The figure for demonstrating the pin-on-disk friction testing machine which concerns on an Example. 実施例1−1,1−2,比較例1−1〜7−1,及び比較例1−2〜7−2に係る摩擦係数の結果を示した図。The figure which showed the result of the friction coefficient which concerns on Examples 1-1 and 1-2, Comparative Examples 1-1 to 7-1, and Comparative Examples 1-2 to 7-2. 実施例2〜4及び比較例8に係る摩擦係数の結果を示した図。The figure which showed the result of the friction coefficient which concerns on Examples 2-4 and the comparative example 8. FIG. 実施例2〜4及び比較例8に係る比摩耗量の結果を示した図。The figure which showed the result of the specific wear amount which concerns on Examples 2-4 and the comparative example 8. FIG. 実施例5〜7及び比較例8に係る摩擦係数の結果を示した図。The figure which showed the result of the friction coefficient which concerns on Examples 5-7 and the comparative example 8. FIG. 実施例5〜7及び比較例8に係る比摩耗量の結果を示した図。The figure which showed the result of the specific wear amount which concerns on Examples 5-7 and the comparative example 8. FIG.

符号の説明Explanation of symbols

10:イオンビームミキシング装置、11:真空チャンバ、12:ホルダ、13:支持台,14:アシスト用イオン源及びガス供給源,15:スパッタイオン源、16:クライオポンプ、30:ピンオンディスク摩擦試験機、31:ボールホルダー、32:ディスクホルダー、33:ステージ、34:ひずみゲージ、35:平行板ばね,37:モータ、38:カップリング、B:ボール試験片(摺動部材)、D:ディスク試験片(摺動部材)、S:シリコンウェハ(基材)、T:カーボンターゲット   10: Ion beam mixing device, 11: Vacuum chamber, 12: Holder, 13: Support base, 14: Assist ion source and gas supply source, 15: Sputter ion source, 16: Cryo pump, 30: Pin-on-disk friction test Machine: 31: Ball holder, 32: Disc holder, 33: Stage, 34: Strain gauge, 35: Parallel leaf spring, 37: Motor, 38: Coupling, B: Ball specimen (sliding member), D: Disc Test piece (sliding member), S: silicon wafer (base material), T: carbon target

Claims (5)

相互に摺動する摺動面のうち少なくとも一方の摺動面に硬質炭素被膜が形成された一対の摺動部材と、該一対の摺動部材の間に存在する潤滑油と、を備えた摺動構造であって、
前記潤滑油は、オレイン酸、リノール酸、及びリノレン酸のうち少なくとも1種を含む植物性潤滑油であることを特徴とする摺動構造。
A sliding member comprising a pair of sliding members having a hard carbon film formed on at least one of the sliding surfaces sliding relative to each other, and a lubricating oil present between the pair of sliding members. Dynamic structure,
The sliding structure, wherein the lubricating oil is a vegetable lubricating oil containing at least one of oleic acid, linoleic acid, and linolenic acid.
前記硬質炭素被膜は、非晶質炭素被膜(DLC被膜)又は窒化炭素被膜(CNx被膜)であることを特徴とする請求項1に記載の摺動構造。   The sliding structure according to claim 1, wherein the hard carbon film is an amorphous carbon film (DLC film) or a carbon nitride film (CNx film). 前記潤滑油は、オレイン酸を少なくとも含んでおり、該オレイン酸は、前記潤滑油に対して70〜85質量%含むことを特徴とする請求項1又は2に記載の摺動構造。   The sliding structure according to claim 1 or 2, wherein the lubricating oil includes at least oleic acid, and the oleic acid is included in an amount of 70 to 85 mass% with respect to the lubricating oil. 前記潤滑油は、リノール酸を少なくとも含んでおり、該リノール酸は、前記潤滑油に対して60〜80質量%含むことを特徴とする請求項1又は2に記載の摺動構造。   The sliding structure according to claim 1 or 2, wherein the lubricating oil contains at least linoleic acid, and the linoleic acid is contained in an amount of 60 to 80 mass% with respect to the lubricating oil. 前記潤滑油は、リノレン酸を少なくとも含んでおり、該リノレン酸は、前記潤滑油に対して30〜60質量%含むことを特徴とする請求項1又は2に記載の摺動構造。   The sliding structure according to claim 1 or 2, wherein the lubricating oil contains at least linolenic acid, and the linolenic acid is contained in an amount of 30 to 60 mass% with respect to the lubricating oil.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10669624B2 (en) 2016-09-28 2020-06-02 Toyota Jidosha Kabushiki Kaisha Sliding member and method for producing the same

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08121617A (en) * 1994-10-24 1996-05-17 Kyocera Corp Ceramics sliding material and sliding device using the same
JP2005168690A (en) * 2003-12-10 2005-06-30 Brother Ind Ltd Sliding component
JP2008093713A (en) * 2006-10-13 2008-04-24 Sumitomo Light Metal Ind Ltd Metal tube expanding method, expanding tool used therefor, and lubricating oil used therefor

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08121617A (en) * 1994-10-24 1996-05-17 Kyocera Corp Ceramics sliding material and sliding device using the same
JP2005168690A (en) * 2003-12-10 2005-06-30 Brother Ind Ltd Sliding component
JP2008093713A (en) * 2006-10-13 2008-04-24 Sumitomo Light Metal Ind Ltd Metal tube expanding method, expanding tool used therefor, and lubricating oil used therefor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10669624B2 (en) 2016-09-28 2020-06-02 Toyota Jidosha Kabushiki Kaisha Sliding member and method for producing the same

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