JPH03285991A - Multi-grade engine oil composition - Google Patents

Multi-grade engine oil composition

Info

Publication number
JPH03285991A
JPH03285991A JP8701390A JP8701390A JPH03285991A JP H03285991 A JPH03285991 A JP H03285991A JP 8701390 A JP8701390 A JP 8701390A JP 8701390 A JP8701390 A JP 8701390A JP H03285991 A JPH03285991 A JP H03285991A
Authority
JP
Japan
Prior art keywords
oil
engine oil
composition
engine
cst
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP8701390A
Other languages
Japanese (ja)
Other versions
JP2866703B2 (en
Inventor
Tetsuo Ueno
上野 哲男
Kazuo Kadokawa
角川 一夫
Yoshitaka Tamoto
芳隆 田本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Idemitsu Kosan Co Ltd
Original Assignee
Idemitsu Kosan Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B1/00Engines characterised by fuel-air mixture compression
    • F02B1/02Engines characterised by fuel-air mixture compression with positive ignition
    • F02B1/04Engines characterised by fuel-air mixture compression with positive ignition with fuel-air mixture admission into cylinder
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B3/00Engines characterised by air compression and subsequent fuel addition
    • F02B3/06Engines characterised by air compression and subsequent fuel addition with compression ignition

Abstract

PURPOSE:To provide the subject composition capable of preventing the abrasion of engine rings especially caused when a Diesel fuel is used and having a good fuel cost by compounding an additive such as zinc dithiophosphate with a specific mineral base oil. CONSTITUTION:The objective composition comprises (A) a mineral base oil having a kinetic viscosity of 2-20cSt at 100 deg.C, a %Cp of 70-80 and a %Ca of <=3 and (B) one kind or more of additives selected from zinc dithiophosphate, a viscosity index improver and a cleansing, dispersing agent preferably comprising a perbasic sulfinate and/or a perbasic sulfonate and an imide compound.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はマルチグレードエンジン油組成物に関し、特に
ディーゼル燃料を用いた場合に生ずるリング摩耗を防止
でき、しかも燃費が良好なマルチグレードエンジン油組
成物に関する。
[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a multigrade engine oil composition, and in particular, a multigrade engine oil composition that can prevent ring wear that occurs when diesel fuel is used and has good fuel efficiency. relating to things.

〔従来の技術及び発明が解決しようとする課題〕従来の
マルチグレードエンジン油(%CP=60〜70)では
、特に大型のエンジンに使用した場合に、エンジン各部
の摩耗、特に、ピストンリングやシリンダーライナーの
摩耗あるいは動弁系の摩耗が大きいという問題とともに
、オイル消費量が多いという問題があった。
[Prior art and problems to be solved by the invention] Conventional multi-grade engine oils (%CP = 60 to 70), especially when used in large engines, cause wear and tear in various parts of the engine, especially piston rings and cylinders. In addition to the problem of large liner wear or valve train wear, there was also the problem of high oil consumption.

また、最近、%C1が85〜90という非常に大きい鉱
油系エンジン油が使用されているが、このエンジン油で
は燃費が悪くなるという問題があった。
Recently, mineral oil-based engine oils with a very high %C1 of 85 to 90 have been used, but this engine oil has the problem of poor fuel efficiency.

〔課題を解決するための手段〕[Means to solve the problem]

本発明者らは、上記従来のマルチグレードエンジン油の
問題を解消し、エンジン各部の摩耗が少なく、またオイ
ル消費量が少なく、しかも燃費の向上したエンジン油を
開発すべく鋭意研究を重ねた。
The inventors of the present invention have conducted intensive research in order to solve the problems of the conventional multi-grade engine oil described above, and to develop an engine oil that causes less wear on various parts of the engine, reduces oil consumption, and has improved fuel efficiency.

その結果、基油として%CFが70〜80である特定の
鉱油を用いることによって、上記目的が達成できること
を見出した。本発明はかかる知見に基いて完成したもの
である。
As a result, it has been found that the above object can be achieved by using a specific mineral oil having a %CF of 70 to 80 as the base oil. The present invention was completed based on this knowledge.

すなわち本発明は、(A) 100℃における動粘度が
2〜20cSt、%C1が70〜80及び%CAが3以
下である鉱油系基油及び(B)ジチオリン酸亜鉛、粘度
指数向上剤及び清浄分散剤から選ばれた少なくとも一種
の添加剤を主成分とするマルチグレードエンジン油組成
物を提供するものである。
That is, the present invention provides (A) a mineral base oil having a kinematic viscosity at 100° C. of 2 to 20 cSt, a %C1 of 70 to 80, and a %CA of 3 or less, and (B) zinc dithiophosphate, a viscosity index improver, and a detergent. The present invention provides a multigrade engine oil composition containing at least one additive selected from dispersants as a main component.

本発明の組成物の(A)成分である基油は、100℃の
粘度が2〜20cSt、好ましくは3〜15cStであ
り、%CPが70〜80、かつ%CAが3以下、好まし
くは%CPが72〜78、かつ%CAが2以下の鉱油で
あれば特に制限はない。
The base oil that is component (A) of the composition of the present invention has a viscosity at 100°C of 2 to 20 cSt, preferably 3 to 15 cSt, a %CP of 70 to 80, and a %CA of 3 or less, preferably % There are no particular limitations as long as the mineral oil has a CP of 72 to 78 and a %CA of 2 or less.

なお、ここで、%CP及び%CAは、ASTM D32
38に規定された方法により求めた値を示す。
In addition, here, %CP and %CA are ASTM D32
The values obtained by the method specified in 38 are shown.

このような鉱油は、各種の方法で製造することができる
が、例えばパラフィン基系または中間基系原油を、通常
の方法で常圧蒸留又は減圧蒸留して得られる潤滑油留分
を、水素化分解処理後、水素化仕上げ又は溶剤抽出等の
処理を行って得ることができる。
Such mineral oils can be produced by various methods, but for example, by hydrogenating a lubricating oil fraction obtained by distilling paraffinic or intermediate-base crude oil by normal pressure distillation or vacuum distillation. After decomposition treatment, it can be obtained by performing treatment such as hydrofinishing or solvent extraction.

この場合、水素化分解の条件(温度、圧力)を適宜選択
すれば、所望の性状(%C7の値)の鉱油を得ることが
できる。
In this case, mineral oil with desired properties (value of %C7) can be obtained by appropriately selecting the conditions for hydrocracking (temperature, pressure).

本発明の(A)成分である基油は、上記で得られる鉱油
を単独又は複数混合して用いてもよいが、上記鉱油と上
記以外の鉱油(つまり、上記%C1の範囲を外れる鉱油
)とを混合したものを用いてもよい。特に上記範囲の%
CPと%CAを有し、100℃における動粘度が2〜8
cStである鉱油と100℃における動粘度が8cSt
以上の鉱油との混合物を用いることが好ましい。但し、
混合後の基油の性状は上記の値を満足することが必要で
ある。
The base oil that is the component (A) of the present invention may be the mineral oil obtained above or in combination, but the above mineral oil and mineral oils other than the above (that is, mineral oils outside the above %C1 range) A mixture of these may also be used. Especially in % of the above range
CP and %CA, and kinematic viscosity at 100°C is 2 to 8.
cSt mineral oil and kinematic viscosity at 100°C is 8 cSt
It is preferable to use a mixture with the above mineral oils. however,
The properties of the base oil after mixing must satisfy the above values.

上記以外の%CP値を示す鉱油としては、通常の溶媒精
製鉱油、水添精製鉱油等を用いることができる。これら
は粘度調整をするのに好都合である。
As the mineral oil exhibiting a %CP value other than the above, ordinary solvent-refined mineral oil, hydrogenated-refined mineral oil, etc. can be used. These are convenient for adjusting viscosity.

また、上記基油を主成分として、少量の合成油(例えば
、ポリα−オレフィン、エステル系合成油等)を配合し
てもよい。
Moreover, a small amount of synthetic oil (for example, polyα-olefin, ester synthetic oil, etc.) may be blended with the base oil as the main component.

次に、本発明の組成物における(B)成分としては、ジ
チオリン酸亜鉛、粘度指数向上剤及び清浄分散剤から選
ばれた少なくとも一種の添加剤を用いる。これらは一種
単独で用いることもできるが、好ましくは二種類を組み
合わせて、さらに好ましくはジチオリン酸亜鉛、粘度指
数向上剤及び清浄分散剤のすべてを組み合わせて使用す
る。
Next, as component (B) in the composition of the present invention, at least one additive selected from zinc dithiophosphate, a viscosity index improver, and a detergent-dispersing agent is used. Although these can be used alone, two types are preferably used in combination, and more preferably all of zinc dithiophosphate, viscosity index improver, and detergent-dispersing agent are used in combination.

ここで、ジチオリン酸亜鉛(ZnDTP)は、酸化防止
剤、耐摩耗剤、極圧剤、腐食防止剤等の機能を併せ持つ
添加剤であり、エンジン油を始め各種の潤滑油に広く利
用されているものを充当すればよい。
Zinc dithiophosphate (ZnDTP) is an additive that has the functions of an antioxidant, anti-wear agent, extreme pressure agent, and corrosion inhibitor, and is widely used in various lubricating oils including engine oil. All you have to do is appropriate it.

一方、粘度指数向上剤としては、特に制限はなく、各種
のものを用いることができ、通常のエンジン油に使用さ
れる粘度指数向上剤を広く用いることができる。その中
でもオレフィンコポリマー(OCP)やポリメタアクリ
レート(PMA)が好適である。
On the other hand, there are no particular limitations on the viscosity index improver, and various types can be used, and a wide variety of viscosity index improvers used in ordinary engine oils can be used. Among them, olefin copolymer (OCP) and polymethacrylate (PMA) are suitable.

また、清浄分散剤についても、特に制限はなく、各種の
ものを用いることができ、通常のエンジン油に使用され
る清浄分散剤、例えばフィネート。
Further, there are no particular restrictions on the detergent dispersant, and various detergent dispersants can be used, such as detergent dispersants used in ordinary engine oils, such as finates.

スルホネート、ナフチネート、サリチレート、ホスホネ
ート及び無灰系分散剤、例えばコハク酸イミド、酸アミ
ド、マンニッヒ塩基(ベンジルアミン型)等をあげるこ
とができる。これらの清浄分散剤は、一種単独で用いて
もよく、あるいは二種以上を混合して用いてもよい。な
お、リング摩耗に対しては、フィネートまたはスルホネ
ート、特に過塩基性フィネートまたは過塩基性スルホネ
ートが好ましい。さらにコハク酸イミド等の無灰系分散
剤を併用すると相乗効果が発現する。
Mention may be made of sulfonates, naphthinates, salicylates, phosphonates and ashless dispersants such as succinimides, acid amides, Mannich bases (benzylamine type) and the like. These cleaning and dispersing agents may be used alone or in combination of two or more. Note that for ring wear, finates or sulfonates, particularly overbased finates or overbased sulfonates, are preferred. Furthermore, when an ashless dispersant such as succinimide is used in combination, a synergistic effect is produced.

上記清浄分散剤中の金属元素はアルカリ金属。The metal element in the above-mentioned cleaning dispersant is an alkali metal.

アルカリ土類金属等が用いられるが、アルカリ土類金属
、特にカルシウムが好ましい、また、清浄分散剤の塩基
価は特に制限されない。高塩基価のものと低塩基価のも
ののいずれか一方、又はこれらの組合わせなど二種以上
を混合して用いてもよい。そのうち、リング摩耗に対し
ては、高塩基価のものが好ましい。
Alkaline earth metals are used, and alkaline earth metals, especially calcium, are preferred, and the base number of the detergent-dispersant is not particularly limited. Either one of those with a high base number or those with a low base number, or a combination thereof, may be used as a mixture of two or more kinds. Among these, those with a high base number are preferred for ring wear.

本発明の組成物において、各成分の配合割合は特に制限
はないが、通常は(B)成分である添加剤を、組成物全
量の2〜30重量%、特に好ましくは5〜20重量%の
範囲で選定する。
In the composition of the present invention, there is no particular restriction on the blending ratio of each component, but the additive (B) is usually added in an amount of 2 to 30% by weight, particularly preferably 5 to 20% by weight of the total amount of the composition. Select by range.

また本発明の組成物は、上記(A)、(B)成分を主成
分とするものであり、基本的にはこの両成分で構成され
るが、さらに必要に応じて、合成油系基油や他の添加剤
、例えば酸化防止剤、錆止め剤、消泡剤、g食切止剤1
着色剤等を適宜配合することもできる。
Further, the composition of the present invention has the above-mentioned components (A) and (B) as main components, and is basically composed of both components, but if necessary, it may also contain a synthetic base oil. and other additives, such as antioxidants, rust inhibitors, antifoaming agents, and anti-corrosion agents 1
A coloring agent or the like may also be added as appropriate.

〔実施例〕〔Example〕

次に本発明を実施例及び比較例によりさらに詳しく説明
する。
Next, the present invention will be explained in more detail with reference to Examples and Comparative Examples.

実施例1及び比較例1〜3 基油と添加剤を第1表に示す割合で配合してエンジン油
組成物を調製した。
Example 1 and Comparative Examples 1 to 3 Engine oil compositions were prepared by blending base oil and additives in the proportions shown in Table 1.

得られたエンジン油組成物について、下記の性能評価を
行った。
The following performance evaluation was performed on the obtained engine oil composition.

(1)エンジン摩耗試験 供試エンジン:三菱4D−30 油温    :105℃ 回転数   :3500rpm 試験時間  :200時間 負荷    :85PS 上記条件で試験を行い、試験終了後の各トップリングの
重量減少量を平均して評価した。
(1) Engine wear test Test engine: Mitsubishi 4D-30 Oil temperature: 105℃ Rotation speed: 3500rpm Test time: 200 hours Load: 85PS The test was conducted under the above conditions, and the weight loss of each top ring after the test was completed. Evaluated on average.

(2)エンジン燃料消費試験 供試エンジン:三菱6D−22TO 油温    :100℃ 回転数   :2200rpm 冷却水温  :80℃ 負荷    :150PS 上記条件下で試験して、燃料消費率(g/PS・時)に
て評価した。
(2) Engine fuel consumption test Test engine: Mitsubishi 6D-22TO Oil temperature: 100℃ Rotation speed: 2200rpm Cooling water temperature: 80℃ Load: 150PS Tested under the above conditions, fuel consumption rate (g/PS・hour) It was evaluated.

(3)オイル消費試験 供試エンジン:三菱6D−22TO 油温    :100℃ 回転数   :220Orpm 冷却水温  :80℃ 負荷    :150PS 試験時間  :100時間 上記条件下で試験して、オイル消費率(g/時)にて評
価した。
(3) Oil consumption test Test engine: Mitsubishi 6D-22TO Oil temperature: 100℃ Rotation speed: 220Orpm Cooling water temperature: 80℃ Load: 150PS Test time: 100 hours Tested under the above conditions, the oil consumption rate (g/ Evaluation was made at

(以下余白) *1:中間基系原油の減圧蒸留留分を、350〜450
℃、60〜200バールで水素化分解し、溶剤膜ろう処
理、溶媒抽出処理して得た芳香族分をほとんど含まない
もの 動粘度(100℃)5cSt、  %C,76゜%CA
0.5 *2:中間基系原油の減圧蒸留留分と脱れき油を混合し
、水素化分解処理、溶剤膜ろう処理を行ったもの 動粘度(100℃) 10cSt、  %C,72゜%
CA3.5 *3:中間基系原油の重質軽油を水素化精製した後、溶
剤膜ろう処理、溶剤抽出処理を行ったもの 動粘度(100℃) 3cSt、  %CP64゜%C
a7 *4:中間基系原油の減圧蒸留留分を、400〜500
℃260〜200バールで水素化分解した後、溶剤膜ろ
う処理を行ったもの 動粘度(100℃) 5 cSt、  %C185%C
aO *5ニオレフインコポリマー(OCP  Mw  10
万)とポリメタアクリレート(PMA Msm 約5万
)を混合して用いた。配合量は、マルチグレードエンジ
ン油を調製するために基油粘度に応じて変更した。
(Left below) *1: The vacuum distillation fraction of intermediate base crude oil is 350 to 450
℃, 60-200 bar hydrogenolysis, solvent membrane brazing treatment, solvent extraction treatment, almost no aromatic content Kinematic viscosity (100℃) 5 cSt, %C, 76゜% CA
0.5 *2: Mixture of vacuum distillation fraction of intermediate base crude oil and deasphalted oil, subjected to hydrocracking treatment and solvent film brazing treatment Kinematic viscosity (100℃) 10cSt, %C, 72゜%
CA3.5 *3: After hydrorefining heavy gas oil of intermediate base crude oil, solvent film waxing treatment and solvent extraction treatment are performed Kinematic viscosity (100℃) 3cSt, %CP64゜%C
a7 *4: Reduce the vacuum distillation fraction of intermediate base crude oil to 400 to 500
Hydrogenolyzed at 260-200 bar ℃ followed by solvent film brazing Kinematic viscosity (100℃) 5 cSt, %C 185%C
aO *5 niolefin copolymer (OCP Mw 10
A mixture of PMA Msm) and polymethacrylate (PMA Msm approximately 50,000) was used. The blending amount was changed depending on the base oil viscosity to prepare a multigrade engine oil.

*6:ジチオリン酸亜鉛、塩基性カルシウムクイネート
塩基性カルシウムスルホネート及びコハク酸イミドを配
合したもの *7:ジチオリン酸亜鉛、カルシウムサリチレート及び
コハク酸イミドを配合したもの *8;ジチオリン酸亜鉛、カルシウムナフチネート及び
コハク酸イミドを配合したもの *9:括弧内の数値は、基油中の各鉱油の配合割合(%
)である。
*6: Formulated with zinc dithiophosphate, basic calcium quinate, basic calcium sulfonate, and succinimide *7: Formulated with zinc dithiophosphate, calcium salicylate, and succinimide *8: Zinc dithiophosphate, Formulated with calcium naphthinate and succinimide *9: The numbers in parentheses indicate the blending ratio (%) of each mineral oil in the base oil.
).

〔発明の効果〕〔Effect of the invention〕

軟土の如く、本発明の組成物をエンジン油として用いれ
ば、エンジン各部の摩耗が少なく、またオイル消費量が
少なく、しかも燃費が著しく向上する。
Like soft soil, if the composition of the present invention is used as an engine oil, there will be less wear on various parts of the engine, less oil consumption, and moreover, fuel efficiency will be significantly improved.

したがって、本発明の組成物はマルチグレードエンジン
油(SAE粘度規格で5W/30.10W/30.IO
W/40等に合致)として有効であり、特に自動車、船
舶、自家発電等のディーゼルエンジン又はアルコール燃
料エンジンの潤滑油として、さらにはガソリンエンジン
の潤滑油として好適に利用できるものである。
Therefore, the composition of the present invention has a multigrade engine oil (SAE viscosity standard of 5W/30.10W/30.IO).
It is effective as a lubricating oil for diesel engines or alcohol-fueled engines used in automobiles, ships, private power generators, etc., and can also be suitably used as a lubricating oil for gasoline engines.

Claims (5)

【特許請求の範囲】[Claims] (1)(A)100℃における動粘度が2〜20cSt
、%C_Pが70〜80及び%C_Aが3以下である鉱
油系基油及び(B)ジチオリン酸亜鉛、粘度指数向上剤
及び清浄分散剤から選ばれた少なくとも一種の添加剤を
主成分とするマルチグレードエンジン油組成物。
(1) (A) Kinematic viscosity at 100°C is 2 to 20 cSt
, a mineral base oil having a %C_P of 70 to 80 and a %C_A of 3 or less, and (B) a mulch containing at least one additive selected from zinc dithiophosphate, a viscosity index improver, and a detergent-dispersant. grade engine oil composition.
(2)清浄分散剤として、過塩基性フィネート及び/又
は過塩基性スルホネートとイミド化合物を用いる請求項
1記載の組成物。
(2) The composition according to claim 1, wherein an overbased finate and/or an overbased sulfonate and an imide compound are used as the detergent and dispersant.
(3)添加剤の配合割合が、組成物全量の2〜30重量
%である請求項1記載の組成物。
(3) The composition according to claim 1, wherein the blending ratio of the additive is 2 to 30% by weight based on the total amount of the composition.
(4)マルチグレードエンジン油組成物が、ディーゼル
エンジン油又はアルコール燃料エンジン油である請求項
1記載の組成物。
(4) The composition according to claim 1, wherein the multigrade engine oil composition is a diesel engine oil or an alcohol fuel engine oil.
(5)基油が、100℃における動粘度が2〜8cSt
、%C_Pが70〜80及び%C_Aが3以下である鉱
油と100℃における動粘度が8cSt以上の鉱油との
混合物である請求項1記載の組成物。
(5) The base oil has a kinematic viscosity of 2 to 8 cSt at 100°C.
The composition according to claim 1, which is a mixture of a mineral oil having a %C_P of 70 to 80 and a %C_A of 3 or less, and a mineral oil having a kinematic viscosity at 100°C of 8 cSt or more.
JP8701390A 1990-03-31 1990-03-31 Multi-grade engine oil composition Expired - Lifetime JP2866703B2 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001059043A1 (en) * 2000-02-09 2001-08-16 Citizen Watch Co., Ltd. Lubricating oil compositions and watch containing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001059043A1 (en) * 2000-02-09 2001-08-16 Citizen Watch Co., Ltd. Lubricating oil compositions and watch containing the same
CN1314787C (en) * 2000-02-09 2007-05-09 西铁城钟表股份有限公司 Lubricating oil compositions and watch containing the same

Also Published As

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JP2866703B2 (en) 1999-03-08

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