JP2006199857A - Gasoline engine oil composition excellent in low fuel expense - Google Patents

Gasoline engine oil composition excellent in low fuel expense Download PDF

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JP2006199857A
JP2006199857A JP2005014076A JP2005014076A JP2006199857A JP 2006199857 A JP2006199857 A JP 2006199857A JP 2005014076 A JP2005014076 A JP 2005014076A JP 2005014076 A JP2005014076 A JP 2005014076A JP 2006199857 A JP2006199857 A JP 2006199857A
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oil
gasoline engine
engine oil
mass
oil composition
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Etsushi Nagatomi
悦史 長富
Fumio Goto
文夫 後藤
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Showa Shell Sekiyu KK
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Showa Shell Sekiyu KK
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Priority to JP2005014076A priority Critical patent/JP2006199857A/en
Priority to CNA2006100089133A priority patent/CN101003761A/en
Priority to EP06100627A priority patent/EP1683852A1/en
Priority to US11/334,938 priority patent/US20060189491A1/en
Priority to SG200600369A priority patent/SG124375A1/en
Publication of JP2006199857A publication Critical patent/JP2006199857A/en
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  • Chemical & Material Sciences (AREA)
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a gasoline engine oil capable of widely reducing the exhaust amount of carbon dioxide from an automobile by a different approach from preceding technologies and excellent in low fuel expense. <P>SOLUTION: This gasoline engine oil is provided by blending at least a salicylate-based cleaner and an ash-less friction regulator, and contains as a base oil component, the base oil showing ≤95 nm oil membrane thickness measured under the conditions of 4.4 m/s sliding velocity, 0.53 GPa hertz pressure and 100°C oil temperature. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、低燃費性に優れたガソリンエンジン油組成物に関する。   The present invention relates to a gasoline engine oil composition having excellent fuel efficiency.

日本の石油需要は年間約2.5億キロリットルであり、そのうちの約4割がガソリンや軽油などの自動車用燃料として消費されており、我国の全炭酸ガス排出量の約2割が運輸部門から排出され、その排出量は年々増加の傾向にある。1997年12月に京都で開催された地球温暖化防止会議では、炭酸ガスの排出量を削減することが議論され、日本の削減目標は1990年の炭酸ガス排出量より6%削減することが合意された。こうした背景から、運輸部門においては2010年までに1995年比で約20%の燃費向上が義務づけられ、ガソリン及びディーゼル内燃機関の更なる低燃費化による自動車から排出される炭酸ガスの削減が最も重要な課題となっている。   Japan's oil demand is about 250 million kiloliters annually, of which about 40% is consumed as fuel for automobiles such as gasoline and light oil, and about 20% of Japan's total carbon dioxide emissions are in the transportation sector. The amount of emissions is increasing year by year. At the Global Warming Prevention Conference held in Kyoto in December 1997, it was discussed to reduce carbon dioxide emissions, and Japan's reduction target was agreed to be 6% lower than carbon dioxide emissions in 1990 It was done. Against this background, the transportation sector is obliged to improve fuel efficiency by about 20% compared to 1995 by 2010, and the most important is to reduce carbon dioxide emissions from automobiles by further reducing fuel consumption of gasoline and diesel internal combustion engines. It is a difficult issue.

自動車からの炭酸ガス排出量の削減、即ち燃費向上の手法として、エンジン燃焼効率の改善、車体及びエンジンの軽量化等数多くのものが挙げられているが、エンジンに充填する潤滑油によるエンジン内部の摩擦低減が最も社会的コスト負担が少ない方法である。特にエンジン油による対応法は、燃焼効率の改善等とは異なり、エンジンデザイン等の変更を必要としないため、手軽でかつ広範囲に適用することができる。   There are many methods to reduce carbon dioxide emissions from automobiles, that is, to improve fuel efficiency, such as improving engine combustion efficiency and reducing the weight of the vehicle body and engine. Friction reduction is the least social cost burden. In particular, the response method using engine oil does not require changes in engine design or the like, unlike improvement in combustion efficiency, and can be applied easily and in a wide range.

従来の省燃費ガソリンエンジン油に使用されている先行技術は、摩擦調整剤、特に有機モリブデン系摩擦調整剤、の添加や、高粘度指数基油の使用により達成されるものが殆どであった。有機モリブデン系摩擦調整剤を配合する先行技術としては特許文献1〜6があるが、有機モリブデン系摩擦調整剤は高価である点が懸念される。   Most of the prior art used in conventional fuel-saving gasoline engine oils is achieved by the addition of friction modifiers, particularly organic molybdenum friction modifiers, and the use of high viscosity index base oils. Although there exists patent documents 1-6 as a prior art which mix | blends an organomolybdenum type | system | group friction modifier, we are anxious about the point that an organic molybdenum type | system | group friction modifier is expensive.

また、ガソリンエンジン油の基油の特性に着目し、粘度指数の大きい基油を用いて上記の課題を解決する代表的な先行技術としては、非特許文献1が挙げられる。   Further, Non-Patent Document 1 is given as a typical prior art that focuses on the characteristics of the base oil of gasoline engine oil and solves the above problems using a base oil having a large viscosity index.

特開2001−348591号公報JP 2001-348591 A 特開2002−12884号公報Japanese Patent Laid-Open No. 2002-12884 特開2002−371292号公報JP 2002-371292 A 特開2001−181664号公報JP 2001-181664 A 特開平8−302378号公報JP-A-8-302378 特開平9−3463号公報Japanese Patent Laid-Open No. 9-3463 SAE TECHNICAL PAPER 951036SAE TECHNICICAL PAPER 951036

本発明の目的は、前記各先行技術と異なったアプローチにより自動車からの炭酸ガス排出量を大幅に削減でき、低燃費性に優れたガソリンエンジン油組成物を提供する点にある。   An object of the present invention is to provide a gasoline engine oil composition that can significantly reduce carbon dioxide emission from an automobile by an approach different from each of the above-described prior arts and is excellent in fuel efficiency.

本発明者らは、ガソリンエンジン油に使用される基油の特性に着目し、鋭意研究を進めた結果、サリシレート系清浄剤と無灰系摩擦調整剤を含むガソリンエンジン油組成物において、基油成分の1つとして、特定条件下で測定した油膜厚さが95nm以下を示す基油を基油成分の5質量%以上含有させると、驚くべきことに低燃費を達成できることを見出し、本発明を完成するに至ったものである。   The inventors of the present invention have paid attention to the characteristics of the base oil used in gasoline engine oil, and as a result of intensive research, the gasoline engine oil composition containing a salicylate-based detergent and an ashless friction modifier contains a base oil. As one of the components, when a base oil having an oil film thickness of 95 nm or less measured under specific conditions is contained in an amount of 5% by mass or more of the base oil component, it has been surprisingly found that low fuel consumption can be achieved. It has come to be completed.

本発明の第1は、基油に、少なくともサリシレート系清浄剤と無灰系摩擦調整剤を配合したガソリンエンジン油組成物であって、基油成分としてすべり速度4.4m/s、ヘルツ圧0.53GPa、油温100℃の条件下で測定した油膜厚さが95nm以下、好ましくは80nm以下、とくに好ましくは70nm以下の基油を含有することを特徴とするガソリンエンジン油組成物に関する。
本発明の前記油膜厚さの測定方法は、具体的には文献SAE TECHNICAL PAPER 961142の図1記載の方法である。
本発明の第2は、すべり速度4.4m/s、ヘルツ圧0.53GPa、油温100℃の条件下で測定した油膜厚さが95nm以下である前記基油が全基油中5質量%以上、好ましくは7質量%以上、とくに好ましくは9質量%以上を占めるものである請求項1記載のガソリンエンジン油組成物に関する。
本発明の第3は、サリシレート系清浄剤の添加量が0.5〜10.0質量%、好ましくは1.0〜8.0質量%、さらに好ましくは1.0〜5.0質量%、無灰系摩擦調整剤の添加量が0.01〜5.0質量%、好ましくは0.05〜2.5質量%、さらに好ましくは0.5〜2.5質量%である請求項1または2記載のガソリンエンジン油組成物に関する。
本発明の第4は、無灰系摩擦調整剤がオレイル基を含む化合物である請求項1または2記載のガソリンエンジン油組成物に関する。
A first aspect of the present invention is a gasoline engine oil composition in which at least a salicylate detergent and an ashless friction modifier are blended with a base oil, and a slip speed of 4.4 m / s and a Hertz pressure of 0 are used as base oil components. The present invention relates to a gasoline engine oil composition characterized by containing a base oil having an oil film thickness of 95 nm or less, preferably 80 nm or less, particularly preferably 70 nm or less measured under the conditions of .53 GPa and an oil temperature of 100 ° C.
The method for measuring the oil film thickness of the present invention is specifically the method described in FIG. 1 of the document SAE TECHNIC PAPA 961142.
In the second aspect of the present invention, the base oil having an oil film thickness of 95 nm or less measured under conditions of a sliding speed of 4.4 m / s, a Hertz pressure of 0.53 GPa, and an oil temperature of 100 ° C. is 5% by mass in the total base oil. The present invention relates to a gasoline engine oil composition according to claim 1, which preferably accounts for 7% by mass or more, particularly preferably 9% by mass or more.
In the third aspect of the present invention, the addition amount of the salicylate detergent is 0.5 to 10.0% by mass, preferably 1.0 to 8.0% by mass, more preferably 1.0 to 5.0% by mass, The addition amount of the ashless friction modifier is 0.01 to 5.0% by mass, preferably 0.05 to 2.5% by mass, more preferably 0.5 to 2.5% by mass. 2. The gasoline engine oil composition according to 2.
The fourth aspect of the present invention relates to the gasoline engine oil composition according to claim 1 or 2, wherein the ashless friction modifier is a compound containing an oleyl group.

サリシレート系清浄剤の増量は、清浄性および酸化安定性向上に効果がある一方、10.0質量%を越える配合ではコスト上昇に対して添加効果が低減する。また、多量の添加は潤滑油中の灰分の増加につながり、ピストンデポジットの生成量増加を引き起こすことから、10.0質量%以下が現実的であり好ましい。また、0.5質量%未満では効果が期待できないため、0.5質量%以上が好ましい。   Increasing the amount of the salicylate detergent is effective in improving the cleanliness and oxidation stability, while the compounding amount exceeding 10.0% by mass reduces the effect of addition with respect to cost increase. Further, since a large amount of addition leads to an increase in ash content in the lubricating oil and causes an increase in the amount of piston deposit produced, 10.0% by mass or less is practical and preferable. Moreover, since an effect is not expectable if it is less than 0.5 mass%, 0.5 mass% or more is preferable.

本発明で使用するサリシレート系清浄剤は、とくにアルキルベンゼンサリチル酸カルシウムが好ましく、日本国特許第1271215号、第1031507号に示す化合物である芳香族カルボン酸と原子番号12から56の間の周期律表第II族の金属との油溶性塩基性塩、全アルカリ価が12mgKOH/g以上に包括される潤滑剤である。しかし本発明においては、アルキルサリシレート金属塩化合物は、カルシウム塩及びマグネシウム塩が好ましい。この理由は、アルキルサリシレートベリリウム塩とバリウム塩の場合は、内燃機関の燃焼による水分と潤滑油の酸化劣化によって形成される弱酸との反応により水溶性塩が生成される可能性があり、この塩は生物毒性の点で環境上好ましくない場合がある。またベリリウム塩の場合は炭酸ガスとの反応により生成される炭酸ベリリウムの結晶硬度が高いため、耐摩耗性を悪化させる懸念がある。それ以外の金属については、金属のコストが高く実用に供することは困難である。本発明においてのサリシレート系清浄剤は、全アルカリ価が50から400mgKOH/gのものが本発明の潤滑性を付与するガソリンエンジン油組成物として好ましい。   The salicylate detergent used in the present invention is particularly preferably calcium alkylbenzene salicylate, and the periodic table between the aromatic carboxylic acids which are compounds shown in Japanese Patent Nos. 1271,215 and 1031507 and atomic numbers 12 to 56 is used. An oil-soluble basic salt with a Group II metal and a lubricant having a total alkali number of 12 mgKOH / g or more. However, in the present invention, the alkyl salicylate metal salt compound is preferably a calcium salt or a magnesium salt. This is because, in the case of alkyl salicylate beryllium salt and barium salt, a water-soluble salt may be generated by the reaction of moisture caused by combustion of the internal combustion engine and weak acid formed by oxidative degradation of the lubricating oil. May be environmentally unfavorable in terms of biotoxicity. In the case of beryllium salt, the crystal hardness of beryllium carbonate produced by the reaction with carbon dioxide gas is high, so there is a concern that the wear resistance is deteriorated. For other metals, the cost of the metal is high and it is difficult to put it to practical use. The salicylate detergent in the present invention preferably has a total alkali number of 50 to 400 mgKOH / g as a gasoline engine oil composition imparting the lubricity of the present invention.

無灰系摩擦調整剤の増量は、低燃費性向上に効果がある一方、5.0質量%を越える配合ではコスト上昇に対して添加効果が低減することから、5.0質量%以下が現実的である。また、0.01質量%未満では効果が期待できないため、0.01質量%以上が好ましい。アルキルカルボン酸、アルキルカルボン酸エステル、アルキルアミン、アルキルアミド、アルキルエーテル等の無灰系摩擦調整剤はアルキル基の長さが長いほど摩擦低減効果が大きいが、アルキル鎖長が長くなるに従い潤滑油への溶解度が低下する。オレイル基はアルキル基の長さとしては、摩擦低減作用を発揮するのに十分な長さを持ち、尚且つ、その分子内に不飽和結合を含んでおり、オレイル基を有する無灰系摩擦調整剤は潤滑油に対しての溶解性が他の無灰系摩擦調整剤に比べて高い。そのため摩擦低減効果に対してその他の無灰系摩擦調整剤よりは有利である。   While increasing the amount of the ashless friction modifier is effective for improving fuel efficiency, the addition of more than 5.0% by mass reduces the effect of adding to the cost increase, so 5.0% by mass or less is a reality. Is. Moreover, since an effect cannot be anticipated if it is less than 0.01 mass%, 0.01 mass% or more is preferable. Ashless friction modifiers such as alkyl carboxylic acids, alkyl carboxylic acid esters, alkyl amines, alkyl amides, and alkyl ethers have a greater effect of reducing friction as the alkyl group length increases. However, as the alkyl chain length increases, lubricating oil Solubility decreases. The oleyl group has an alkyl group length sufficient to exert a friction reducing action, and also contains an unsaturated bond in the molecule, and has an oleyl group and has an ashless friction control. The agent has higher solubility in lubricating oil than other ashless friction modifiers. Therefore, it is more advantageous than other ashless friction modifiers for the friction reduction effect.

本発明に用いる基油としては、鉱油系潤滑油、合成油系潤滑油又はこれらの中から選ばれる2種以上の混合物等が使用でき、また、そのなかで必ず添加しなければならない上記の条件下で測定された油膜厚さの条件を満たす基油についても同様である。例えば、鉱油系潤滑油、鉱油系潤滑油と芳香族分非含有合成油系潤滑油との混合油、芳香族分含有合成油系潤滑油と芳香族分非含有合成油系潤滑油との混合油等が例示できる。   As the base oil used in the present invention, mineral oil-based lubricating oil, synthetic oil-based lubricating oil, or a mixture of two or more selected from these can be used. The same applies to the base oil that satisfies the conditions of the oil film thickness measured below. For example, mineral oil-based lubricating oil, mixed oil of mineral oil-based lubricating oil and non-aromatic synthetic oil-based lubricating oil, mixing of aromatic-containing synthetic oil and non-aromatic-containing synthetic oil-based lubricating oil An oil etc. can be illustrated.

一般にエンジン油には基油、清浄剤及び摩擦調整剤のほかに耐摩耗剤、無灰系分散剤、酸化防止剤、粘度指数向上剤、流動点降下剤、消泡剤等が配合されているが、本発明の潤滑組成物にも、所望によりこれらの各種添加剤を適量加えることができる。   In general, engine oils contain base oils, detergents and friction modifiers, as well as antiwear agents, ashless dispersants, antioxidants, viscosity index improvers, pour point depressants, antifoaming agents, etc. However, an appropriate amount of these various additives can be added to the lubricating composition of the present invention as desired.

耐摩耗剤としては亜鉛ジチオフォスフェート(ZnDTP)が一般に配合されているが、本発明においては、炭素数3から12のアルキル基を有し、そのアルコール残基が2級(Sec−ZnDTP)または1級(Pri−ZnDTP)、もしくはそれらの混合物が配合されていることが好ましく、添加量としてはりん元素量で0.03〜0.1質量%を配合することが好ましく、とくにりん元素量で0.03〜0.08質量%が最も好ましい。   As the antiwear agent, zinc dithiophosphate (ZnDTP) is generally blended, but in the present invention, it has an alkyl group having 3 to 12 carbon atoms, and the alcohol residue thereof is secondary (Sec-ZnDTP) or Primary (Pri-ZnDTP) or a mixture thereof is preferably blended, and the addition amount is preferably 0.03 to 0.1% by mass in terms of elemental phosphorus, and especially in terms of elemental phosphorus. 0.03-0.08 mass% is the most preferable.

無灰系分散剤としては通常2〜10質量%の割合で配合し、その種類としては日本国特許第1367796号、第1667140号、第1302811号、第1743435号に示されるポリアルケニルこはく酸イミド、ポリアルケニルこはく酸エステルなどが挙げられ、またこれらの化合物のほう素化誘導体を本発明の潤滑性を付与するガソリンエンジン油組成物に配合することも可能である。   As the ashless dispersant, it is usually blended at a ratio of 2 to 10% by mass, and the types thereof include polyalkenyl succinimides shown in Japanese Patent Nos. 1367796, 1667140, 1302811, and 1743435, Examples thereof include polyalkenyl succinic acid esters, and boronated derivatives of these compounds can be blended in the gasoline engine oil composition imparting the lubricity of the present invention.

酸化防止剤としては、2−t−ブチルフェノール、2−t−ブチル−4−メチルフェノール、2−t−ブチル−5−メチルフェノール、2,4−ジ−t−ブチルフェノール、2,4−ジメチル−6−t−ブチルフェノール、2−t−ブチル−4−メトキシフェノール、3−t−ブチル−4−メトキシフェノール、2,6−ジ−t−ブチルフェノール、2,6−ジ−t−ブチル−4−メチルフェノール、2,6−ジ−t−ブチル−4−エチルフェノール、2,6−ジ−t−ブチル−4−メトキシフェノール、2,6−ジ−t−ブチル−4−エトキシフェノール、3,5−ジ−t−ブチル−4−ヒドロキシベンジルメルカプト−オクチルアセテート、n−ドデシル−3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート、2′−エチルヘキシル−3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート、2,6−ジ−t−ブチル−α−ジメチルアミノ−p−クレゾール、4,4′−メチレンビス(2,6−ジ−t−ブチルフェノール)、4,4′−ビス(2,6−ジ−t−ブチルフェノール)、2,2−ビス(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロパン、4,4′−シクロヘキシリデンビス(2,6−t−ブチルフェノール)、ヘキサメチレングリコールビス[3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート](チバ・スペシャルティー・ケミカルズ社製:Irganox L109)、2,2′−チオ−[ジエチル−3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート](チバ・スペシャルティー・ケミカルズ社製:Irganox L115)、テトラキス[メチレン−3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート]メタン(チバ・スペシャルティー・ケミカルズ社製:Irganox L101)、1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)ベンゼン(シェル・ジャパン社製:Ionox330)、ビス−[3,3′−ビス−(4′−ヒドロキシ−3′−t−ブチルフェニル)ブチリックアシッド]グリコールエステル、2−(3′,5′−ジ−t−ブチル−4−ヒドロキシフェニル)メチル−4−(2″,4″−ジ−t−ブチル−3″−ヒドロキシフェニル)メチル−6−t−ブチルフェノール、2,6−ビス(2′−ヒドロキシ−3′−t−ブチル−5′−メチル−ベンジル)−4−メチルフェノール等のフェノール系酸化防止剤、p,p′−ジオクチル−ジフェニルアミン、p,p′−ジ−α−メチルベンジル−ジフェニルアミン、N−p−ブチルフェニル−N−p′−オクチルフェニルアミン、モノ−t−ブチルジフェニルアミン、モノオクチルジフェニルアミン、ジ(2,4−ジエチルフェニル)アミン、ジ(2−エチル−4−ノニルフェニル)アミン、オクチルフェニル−1−ナフチルアミン、N−t−ドデシルフェニル−1−ナフチルアミン、1−ナフチルアミン、フェニル−1−ナフチルアミン、フェニル−2−ナフチルアミン、N−ヘキシルフェニル−2−ナフチルアミン、N−オクチルフェニル−2−ナフチルアミン、N,N′−ジイソプロピル−p−フェニレンジアミン、N,N′−ジフェニル−p−フェニレンジアミン等のアミン系酸化防止剤、さらにはモリブデンジチオカーバメートやモリブデンアルキルアミン塩等の有機モリブデン化合物等を挙げられ、これらを単独もしくは数種類組み合わせて0.01〜5質量%、好ましくは0.1〜3質量%の割合で使用することができる。   Antioxidants include 2-t-butylphenol, 2-t-butyl-4-methylphenol, 2-t-butyl-5-methylphenol, 2,4-di-t-butylphenol, 2,4-dimethyl- 6-t-butylphenol, 2-t-butyl-4-methoxyphenol, 3-t-butyl-4-methoxyphenol, 2,6-di-t-butylphenol, 2,6-di-t-butyl-4- Methylphenol, 2,6-di-t-butyl-4-ethylphenol, 2,6-di-t-butyl-4-methoxyphenol, 2,6-di-t-butyl-4-ethoxyphenol, 3, 5-di-tert-butyl-4-hydroxybenzylmercapto-octyl acetate, n-dodecyl-3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate, 2 -Ethylhexyl-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, 2,6-di-t-butyl-α-dimethylamino-p-cresol, 4,4'-methylenebis (2 , 6-di-t-butylphenol), 4,4'-bis (2,6-di-t-butylphenol), 2,2-bis (3,5-di-t-butyl-4-hydroxyphenyl) propane 4,4'-cyclohexylidenebis (2,6-t-butylphenol), hexamethylene glycol bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] (Ciba Specialty) * Chemicals: Irganox L109), 2,2'-thio- [diethyl-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] Ciba Specialty Chemicals: Irganox L115), tetrakis [methylene-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] methane (Ciba Specialty Chemicals: Irganox L101) ), 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene (manufactured by Shell Japan: Ionox 330), bis- [3,3 '-Bis- (4'-hydroxy-3'-t-butylphenyl) butyric acid] glycol ester, 2- (3', 5'-di-t-butyl-4-hydroxyphenyl) methyl-4- ( 2 ″, 4 ″ -di-tert-butyl-3 ″ -hydroxyphenyl) methyl-6-tert-butylphenol, 2,6-bis (2 -Hydroxy-3'-t-butyl-5'-methyl-benzyl) -4-methylphenol and other phenolic antioxidants, p, p'-dioctyl-diphenylamine, p, p'-di-α-methylbenzyl -Diphenylamine, Np-butylphenyl-Np'-octylphenylamine, mono-t-butyldiphenylamine, monooctyldiphenylamine, di (2,4-diethylphenyl) amine, di (2-ethyl-4-nonyl) Phenyl) amine, octylphenyl-1-naphthylamine, Nt-dodecylphenyl-1-naphthylamine, 1-naphthylamine, phenyl-1-naphthylamine, phenyl-2-naphthylamine, N-hexylphenyl-2-naphthylamine, N-octyl Phenyl-2-naphthylamine, N, N'-diiso Examples include amine-based antioxidants such as propyl-p-phenylenediamine and N, N′-diphenyl-p-phenylenediamine, and organic molybdenum compounds such as molybdenum dithiocarbamate and molybdenum alkylamine salts. Several types can be used in combination at 0.01 to 5% by mass, preferably 0.1 to 3% by mass.

粘度指数向上剤としては、例えば日本国特許第954077号、第1031507号、第1468752号、第1764494号、第1751082号に記載されているスチレン−ブタジエン共重合体、スチレン−イソプレン星状共重合体、ポリメタクリレート系、エチレン−プロピレン共重合体などが挙げられ、これらは1から20質量%の割合で使用される。またこれらのものに窒素原子や酸素原子を分子中に含んだ極性モノマーを共重合させた分散型粘度指数向上剤についても同じように使用することができる。   Examples of the viscosity index improver include styrene-butadiene copolymers and styrene-isoprene star copolymers described in Japanese Patent Nos. 954077, 1031507, 1468752, 1764494, and 1751082. , Polymethacrylates, ethylene-propylene copolymers and the like, and these are used in a proportion of 1 to 20% by mass. Further, a dispersion type viscosity index improver obtained by copolymerizing a polar monomer containing a nitrogen atom or an oxygen atom in the molecule can be used in the same manner.

流動点降下剤としては、日本国特許第1195542号、第1264056号に記載されているメタクリレート重合体などが使用される。防錆剤として、アルケニルこはく酸またはその部分エステル、ベンゾトリアゾール系化合物、チアジアゾール系化合物、などが使用される。   As the pour point depressant, methacrylate polymers described in Japanese Patent Nos. 1195542 and 1264056 are used. As the rust inhibitor, alkenyl succinic acid or a partial ester thereof, benzotriazole compound, thiadiazole compound, and the like are used.

消泡剤としては、ジメチルポリシクロヘキサン、ポリアクリレート等が使用される。   As the antifoaming agent, dimethylpolycyclohexane, polyacrylate or the like is used.

本発明の特徴を一層明らかにするために、現在当該分野で汎用されている低燃費ガソリンエンジン油組成物と本発明の1例であるガソリンエンジン油組成物を対比すると、おおむね下記表1のようになる。   In order to further clarify the features of the present invention, a comparison between a fuel-efficient gasoline engine oil composition that is currently widely used in the field and a gasoline engine oil composition that is an example of the present invention is as shown in Table 1 below. become.

Figure 2006199857
Figure 2006199857

(1)本発明により優れた低燃費性を有するガソリンエンジン油組成物が提供できた。
(2)本発明は、潤滑油の基本成分である基油の特性に着目し、特有の添加剤組成と組み
合わせることにより、優れた低燃費性を有する潤滑油組成物を見出した。
(3)本発明は、有機モリブデン化合物のような無灰系でない摩擦低減剤を用いなくても
、充分目的を達成することができた。
(1) A gasoline engine oil composition having excellent fuel efficiency can be provided by the present invention.
(2) The present invention pays attention to the characteristics of the base oil, which is a basic component of the lubricating oil, and has found a lubricating oil composition having excellent fuel efficiency by combining with a specific additive composition.
(3) The present invention can sufficiently achieve the object without using a non-ashless friction reducing agent such as an organic molybdenum compound.

以下に実施例と比較例を挙げて本発明を詳細に説明するが、本発明はこれにより何ら限定されるものではない。   Hereinafter, the present invention will be described in detail with reference to examples and comparative examples, but the present invention is not limited thereto.

本発明で採用した評価試験法は以下の通りである。
基油の油膜厚さは文献SAE TECHNICAL PAPER 961142に記載された方法(文献中の図1の方法)により測定した。100℃高温高せん断粘度は、ASTM D5481試験法により求めた。
100℃及び40℃の動粘度は、JIS K2283試験法により求めた。
粘度指数はJIS K2283試験法により求めた。
低燃費性の評価
図1に低燃費性を評価するためのエンジントルク損失試験装置の概要を示す。直打式動弁機構をもつ3.0Lエンジンを使用し、エンジン油温80℃でエンジン回転数を電気モータでアイドル回転数から2800rpmまで制御し、発生する摩擦損失トルクを計測することにより、エンジン油の摩擦特性を評価した。
結果は比較例1に対して各エンジン回転数におけるエンジン損失トルクがどれだけ改善されたかを、エンジン損失トルク改善率として示した。
The evaluation test methods employed in the present invention are as follows.
The oil film thickness of the base oil was measured by the method described in the document SAE TECHNICICAL PAPER 961142 (the method of FIG. 1 in the document). The 100 ° C. high temperature high shear viscosity was determined by ASTM D5481 test method.
The kinematic viscosity at 100 ° C. and 40 ° C. was determined by the JIS K2283 test method.
The viscosity index was determined by the JIS K2283 test method.
Evaluation of low fuel consumption FIG. 1 shows an outline of an engine torque loss test apparatus for evaluating low fuel consumption. By using a 3.0L engine with a direct-acting valve mechanism, controlling the engine speed from an idle speed to 2800 rpm with an electric motor at an engine oil temperature of 80 ° C, and measuring the generated friction loss torque, the engine The friction characteristics of the oil were evaluated.
The results show how much the engine loss torque at each engine speed was improved as compared with Comparative Example 1 as the engine loss torque improvement rate.

本発明の実施例と比較例で使用した基油の性状を表2に、本発明の実施例と比較例の組成を表3におよびその低燃費試験結果を表4に示す。表4は比較例1に対する各実施例、比較例の改善程度を示すものであるため、表4中の比較例1のデータは丁度0となる。   Table 2 shows the properties of the base oils used in the examples and comparative examples of the present invention, Table 3 shows the compositions of the examples and comparative examples of the present invention, and Table 4 shows the results of the low fuel consumption test. Since Table 4 shows the degree of improvement of each Example and Comparative Example with respect to Comparative Example 1, the data of Comparative Example 1 in Table 4 is exactly 0.

Figure 2006199857
Figure 2006199857

Figure 2006199857
Figure 2006199857

Figure 2006199857
表中の5W−30および0W−30はSEAエンジン油の粘度分類におけるSEAエンジン粘度番号である。
アイドルとは、軸出力を出さず、エンジンの機械損失に打ち克って設定回転数を維持している状態をいう。
Figure 2006199857
5W-30 and 0W-30 in the table are SEA engine viscosity numbers in the viscosity classification of SEA engine oil.
Idle means a state in which the set rotational speed is maintained without overcoming the mechanical loss of the engine without producing shaft output.

表3中のカルシウムサリシレートはインフィニアム・ジャパン社より入手したInfineum M7101、カルシウムスルフォネートは日本ルーブリゾール社より入手したLz52である。
表3中の無灰系摩擦調整剤は花王社より入手したオレイン酸エステル エマゾールMO−50である。
表3中の粘度指数向上剤は、デグサ・ジャパン社より入手したポリメタアクリレート Viscoplex 6−950、無灰系分散剤は、インフィニアム・ジャパン社より入手したポリアルケニルこはく酸イミド Infineum M7107、耐摩耗剤(ZnDTP)は、日本ルーブリゾール社より入手したLz1395、酸化防止剤は、チバスペシャルティー・ケミカルズ社から入手したフェノール系酸化防止剤 Irganox L135、流動点降下剤はインフィニアム・ジャパン社より入手したポリメタアクリレート Infineum V351、消泡剤はダウコーニング社より入手したジメチルポリシクロヘキサンである。
The calcium salicylate in Table 3 is Infineum M7101 obtained from Infinium Japan, and the calcium sulfonate is Lz52 obtained from Nippon Lubrizol.
The ashless friction modifier in Table 3 is oleic acid ester Emazole MO-50 obtained from Kao Corporation.
The viscosity index improver in Table 3 is polymethacrylate Viscoplex 6-950 obtained from Degussa Japan, and the ashless dispersant is polyalkenyl succinimide Infineum M7107 obtained from Infinium Japan, wear-resistant Agent (ZnDTP) was obtained from Nippon Lubrizol, Lz1395, the antioxidant was a phenolic antioxidant Irganox L135 obtained from Ciba Specialty Chemicals, and the pour point depressant was obtained from Infinium Japan. Polymethacrylate Infineum V351, the antifoaming agent, is dimethylpolycyclohexane obtained from Dow Corning.

図1は、低燃費性を評価するために用いるエンジントルク損失試験装置の概略図である。FIG. 1 is a schematic diagram of an engine torque loss test apparatus used for evaluating low fuel consumption.

Claims (4)

基油に、少なくともサリシレート系清浄剤と無灰系摩擦調整剤を配合したガソリンエンジン油組成物であって、基油成分としてすべり速度4.4m/s、ヘルツ圧0.53GPa、油温100℃の条件下で測定した油膜厚さが95nm以下の基油を含有することを特徴とするガソリンエンジン油組成物。   A gasoline engine oil composition in which at least a salicylate-based detergent and an ashless friction modifier are blended with a base oil, a sliding speed of 4.4 m / s, a Hertz pressure of 0.53 GPa, and an oil temperature of 100 ° C. as a base oil component A gasoline engine oil composition comprising a base oil having an oil film thickness of 95 nm or less measured under the above conditions. すべり速度4.4m/s、ヘルツ圧0.53GPa、油温100℃の条件下で測定した油膜厚さが95nm以下である前記基油が全基油中5質量%以上を占めるものである請求項1記載のガソリンエンジン油組成物。   The base oil having an oil film thickness of 95 nm or less measured under conditions of a sliding speed of 4.4 m / s, a Hertz pressure of 0.53 GPa, and an oil temperature of 100 ° C. occupies 5% by mass or more of the total base oil. Item 4. A gasoline engine oil composition according to Item 1. サリシレート系清浄剤の添加量が0.5〜10.0質量%、無灰系摩擦調整剤の添加量が0.01〜5.0質量%である請求項1または2記載のガソリンエンジン油組成物。   The gasoline engine oil composition according to claim 1 or 2, wherein the addition amount of the salicylate detergent is 0.5 to 10.0 mass% and the addition amount of the ashless friction modifier is 0.01 to 5.0 mass%. object. 無灰系摩擦調整剤がオレイル基を含む化合物である請求項1または2記載のガソリンエンジン油組成物。
The gasoline engine oil composition according to claim 1 or 2, wherein the ashless friction modifier is a compound containing an oleyl group.
JP2005014076A 2005-01-21 2005-01-21 Gasoline engine oil composition excellent in low fuel expense Pending JP2006199857A (en)

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