JPH08127789A - Lubricating oil composition - Google Patents

Lubricating oil composition

Info

Publication number
JPH08127789A
JPH08127789A JP7214565A JP21456595A JPH08127789A JP H08127789 A JPH08127789 A JP H08127789A JP 7214565 A JP7214565 A JP 7214565A JP 21456595 A JP21456595 A JP 21456595A JP H08127789 A JPH08127789 A JP H08127789A
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JP
Japan
Prior art keywords
type
molecular weight
monotype
blended
long chain
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
JP7214565A
Other languages
Japanese (ja)
Other versions
JP2842585B2 (en
Inventor
Kazushi Okato
一志 岡登
Makoto Tsuji
誠 辻
Hiroshi Ogasa
博司 小笠
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.)
Honda Motor Co Ltd
Original Assignee
Honda Motor Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Honda Motor Co Ltd filed Critical Honda Motor Co Ltd
Priority to JP7214565A priority Critical patent/JP2842585B2/en
Priority to DE69513588T priority patent/DE69513588T2/en
Priority to EP95113919A priority patent/EP0699738B1/en
Publication of JPH08127789A publication Critical patent/JPH08127789A/en
Application granted granted Critical
Publication of JP2842585B2 publication Critical patent/JP2842585B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M161/00Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M133/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M133/12Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to a carbon atom of a six-membered aromatic ring
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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/52Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
    • C10M133/56Amides; Imides
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    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/10Thio derivatives
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    • C10M145/00Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
    • C10M145/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M145/10Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
    • C10M145/12Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate monocarboxylic
    • C10M145/14Acrylate; Methacrylate
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    • C10M155/00Lubricating compositions characterised by the additive being a macromolecular compound containing atoms of elements not provided for in groups C10M143/00 - C10M153/00
    • C10M155/02Monomer containing silicon
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/087Boron oxides, acids or salts
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/084Acrylate; Methacrylate
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    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
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    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/065Phenyl-Naphthyl amines
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    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/066Arylene diamines
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    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/068Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings having amino groups bound to polycyclic aromatic ring systems, i.e. systems with three or more condensed rings
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • C10M2229/051Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon containing halogen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • C10M2229/052Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • C10M2229/053Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon containing sulfur
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/05Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
    • C10M2229/054Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon containing phosphorus
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids

Abstract

PURPOSE: To improve the adsorption per unit area, coefficient of friction, and viscosity index by incorporating bis type and mono type alkenylsuccinimides and a particular polydimethylsiloxane into a base oil. CONSTITUTION: A bis type alkenylsuccinic acid with the average mol.wt. of the alkenyl group being 1000 to 1500, a mono type alkenylsuccinic acid with the average mol.wt. of the alkenyl group being 2000 to 2500, a low-mol.wt. polydimethylsiloxane having a kinematic viscosity of 10 to 100cSt, and a high- mol.wt. polydimethylsiloxane having a kinematic viscosity of 5000 to 20000cSt are incorporated as an additive into a base oil having a kinematic viscosity (100 deg.C) of not less than 3cSt.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、自動変速機の潤滑
油として使用する潤滑油組成物に関する。
TECHNICAL FIELD The present invention relates to a lubricating oil composition used as a lubricating oil for an automatic transmission.

【0002】[0002]

【従来の技術】自動車、モーターボート、農業機械等で
使用される自動変速機用潤滑油:ATF(Automa
tic Transmission Fluid)に、
無灰系分散剤を用いることは公知である。又、摩擦係数
(μ)を高くする目的で金属系清浄剤等を用いたり、こ
れらの添加剤と組合せて用いることも公知である。例え
ば特開平3−39396号公報等。
Lubricating oil for automatic transmissions used in automobiles, motor boats, agricultural machines, etc .: ATF (Automata)
tic Transmission Fluid)
The use of ashless dispersants is known. It is also known to use a metal-based detergent or the like for the purpose of increasing the friction coefficient (μ), or to use it in combination with these additives. For example, JP-A-3-39396, etc.

【0003】[0003]

【発明が解決しようとする課題】しかしながら無灰系分
散剤は、金属系清浄剤よりも比較的摩擦係数を向上させ
る効果が高いので、既存のATF以上に摩擦係数を向上
させるには、無灰系分散剤の吸着量を増して、摩擦係数
を向上させることが考えられる。但し、無灰系分散剤の
添加量を増加させたのでは、ATF中の他の添加剤と形
成する系のバランスがくずれ、安定性の悪いATFにな
ってしまう。
However, since the ashless dispersant has a relatively higher effect of improving the friction coefficient than the metallic detergent, the ashless dispersant can be used to improve the friction coefficient more than the existing ATF. It is considered that the adsorption amount of the system dispersant is increased to improve the friction coefficient. However, if the addition amount of the ashless dispersant is increased, the balance between the system formed with other additives in the ATF is lost and the stability of the ATF becomes poor.

【0004】このようにATF中に無灰系分散剤、又は
摩擦調整剤(FM剤)や金属系清浄剤を配合した場合、
静摩擦係数(μs)、及び動摩擦係数(μd)の値がそ
れほど高くならず、トルク容量の確保や、クラッチの小
径化、クラッチ枚数の低減といったトランスミッシヨン
のコンパクト化、及び軽量化には不向きであった。又、
無灰系分散剤の添加量を増加する等して摩擦係数を無理
に高くしようとすると、安定性の悪いATFになってし
まう不具合がある。
As described above, when an ashless dispersant, a friction modifier (FM agent) or a metal detergent is mixed in ATF,
The values of static friction coefficient (μs) and dynamic friction coefficient (μd) are not so high, and are not suitable for securing torque capacity, downsizing of clutch such as reduction of clutch diameter and number of clutches, and weight reduction. It was or,
If the friction coefficient is forcibly increased by increasing the addition amount of the ashless dispersant or the like, there is a problem that ATF with poor stability results.

【0005】一方、こはく酸イミド骨格を持つ添加剤に
は、平均分子量が5500以上のものもある。例えば特
開平6−240275号公報に記載された潤滑油組成物
は、アミン化合物 0.01〜3.0重量%、過塩基性
カルシウムフェネート 0.05〜5.0重量%と、こ
はく酸イミド系無灰分散剤 0.5〜5.0重量%、及
びB遮蔽型こはく酸イミド無灰分散剤 0.5〜5.0
重量%とを配合したものである。そしてこのこはく酸イ
ミドは、炭素数500〜5000(分子量7000〜7
0000)のものを使用している。
On the other hand, some additives having a succinimide skeleton have an average molecular weight of 5500 or more. For example, the lubricating oil composition described in JP-A-6-240275 has an amine compound of 0.01 to 3.0% by weight, an overbased calcium phenate of 0.05 to 5.0% by weight, and a succinimide. Ashless dispersant 0.5 to 5.0% by weight, and B-shielding succinimide ashless dispersant 0.5 to 5.0
% By weight. This succinimide has a carbon number of 500 to 5000 (molecular weight of 7000 to 7).
0000) is used.

【0006】しかしながら分散剤として分子量7000
〜70000のこはく酸イミドを100℃の動粘度が3
cSt以上の基油に添加する場合、これらの添加剤を前
述の比較的低分子量の分散剤と同程度の量だけ配合する
と、ATF全体の粘度が上昇してしまう。そこで、粘度
指数向上剤(ポリメタクリレート)の量を少なくする訳
であるが、そうすると今度は、ATFとして所望の粘度
指数を達成できなくなる。
However, the dispersant has a molecular weight of 7,000.
~ 70,000 succinimide has a kinematic viscosity of 3 at 100 ° C.
When added to a base oil having a cSt or more, if these additives are added in an amount similar to that of the above-mentioned relatively low molecular weight dispersant, the viscosity of the entire ATF will increase. Therefore, the amount of the viscosity index improver (polymethacrylate) is reduced, but then the desired viscosity index cannot be achieved as the ATF.

【0007】ATFの粘度指数を高く設定できないと、
温度による粘度の変化が大きくなり、高温(例えば10
0℃)の動粘度を揃えると(通常7cSt程度)、低温
の粘度が上昇してしまう。この場合、トランスミッシヨ
ンの油圧制御が、高摩擦係数、且つ高粘度指数のATF
に比べてスムーズにいかなくなる不都合がある。この不
具合が起こる粘度指数(VI)の分岐点は、本発明の高
摩擦係数ATFの場合、VI=190前後である。即
ち、200以上あれば好ましい粘度指数であり、190
に満たなければ高摩擦係数ATFの場合、不具合が生じ
る。
If the viscosity index of ATF cannot be set high,
Viscosity changes greatly with temperature, resulting in high temperatures (for example, 10
If the kinematic viscosity at 0 ° C. is made uniform (usually about 7 cSt), the low temperature viscosity will increase. In this case, the hydraulic control of the transmission is the ATF having a high friction coefficient and a high viscosity index.
There is a disadvantage that it does not go smoothly compared to. The branch point of the viscosity index (VI) at which this problem occurs is around VI = 190 in the case of the high friction coefficient ATF of the present invention. That is, a viscosity index of 200 or more is preferable and 190
If it does not satisfy the above condition, a problem occurs when the coefficient of friction is high.

【0008】[0008]

【課題を解決するための手段】そこで本発明者は、添加
量を変えずに、無灰系分散剤特有のタイプ(後述する8
タイプ)に着目し、これを特定の組合せによって吸着量
を向上させ、延いてはATFの摩擦係数の向上を実現さ
せることが出来た。ここで無灰系分散剤として用いられ
るアルケニルこはく酸イミドは、アルケニル基が短鎖で
平均分子量1000〜1500、長鎖で平均分子量20
00〜2500のものを配合する必要がある。
Therefore, the inventor of the present invention has proposed a type peculiar to the ashless dispersant (see 8
It was possible to improve the adsorption amount by using a specific combination of these types, and eventually to improve the friction coefficient of ATF. The alkenyl succinimide used here as the ashless dispersant has a short-chain alkenyl group with an average molecular weight of 1000 to 1500 and a long-chain alkenyl group with an average molecular weight of 20.
It is necessary to blend those of 00 to 2500.

【0009】本発明によれば、金属系清浄剤を含まない
ので、こはく酸イミドの吸着が阻害されないから、摩擦
係数(μ)が向上する。又、摩擦調整剤(FM剤:アル
キルアミン)の添加量は、0.1〜1.0重量%である
が、添加量が0.1重量%よりも小さいと μ0/μd
1 となり、添加量を1.0重量%よりも大きくする
と、摩擦係数(μ)を低下させる働きが大きくなる。更
に粘度指数を向上させるには、低粘度の基油を使用すれ
ば向上するが、揮発性であるので、実用上問題がある。
According to the present invention, since the metallic detergent is not contained, the adsorption of succinimide is not hindered, and the friction coefficient (μ) is improved. The addition amount of the friction modifier (FM agent: alkylamine) is 0.1 to 1.0% by weight, but if the addition amount is less than 0.1% by weight, μ 0 / μ d >.
1 and when the amount added is more than 1.0% by weight, the function of lowering the friction coefficient (μ) becomes large. In order to further improve the viscosity index, the use of a low-viscosity base oil improves, but it is practically problematic because it is volatile.

【0010】潤滑油組成物中に無灰系分散剤として用い
られるアルケニルこはく酸イミドには、次のタイプのも
のがある。 I)モノタイプ II)ビスタイプ(こはく酸イミド骨格が2ケ) III)B系タイプ(ボロンが導入されたタイプ) IV)非B系タイプ V)長鎖タイプ(アルケニル鎖の長さが平均分子量で2
000〜2500) VI)非長鎖タイプ(アルケニル鎖の長さが平均分子量
で1000〜1500程度 I)〜VI) の化学式は
次の通りである。
Alkenyl succinimides used as ashless dispersants in lubricating oil compositions include the following types: I) Monotype II) Bis type (two succinimide skeletons) III) B type (boron-introduced type) IV) Non-B type V) Long chain type (length of alkenyl chain is average molecular weight) In 2
000 to 2500) VI) Non-long chain type (alkenyl chain length is about 1000 to 1500 in terms of average molecular weight I) to VI) has the following chemical formula.

【0011】[0011]

【化1】 Embedded image

【0012】ところで、アルケニルこはく酸イミドのタ
イプは、(a)B系ビスタイプ、(b)長鎖モノタイプ
を含めて次の8種類がある。 (a)B系ビスタイプ (b)長鎖モノタイプ (c)非長鎖非B系ビスタイプ (d)非B系モノタイプ (e)長鎖ビスタイプ (f)B系モノタイプ (g)長鎖B系ビスタイプ (h)長鎖B系モノタイプ
There are the following eight types of alkenyl succinimide, including (a) B type bis type and (b) long chain monotype. (A) B-type bis type (b) Long-chain monotype (c) Non-long-chain non-B-type bis type (d) Non-B-type monotype (e) Long-chain bistype (f) B-type monotype (g) Long chain B type bis type (h) Long chain B type mono type

【0013】この8種類の組合せは、次のようになる。 8種類中2種類の組合せ:82=28 8種類中3種類の組合せ:83=56 但し、4種類以上の組合せは、効果がないことが判って
いる。この28+56=84通りの組合せは、更に組合
せた添加量の配合の割合を変化させることが出来る。
The eight combinations are as follows. Combination of 2 out of 8 types: 8 C 2 = 28 Combination of 3 out of 8 types: 8 C 3 = 56 However, it is known that combinations of 4 or more types have no effect. With this 28 + 56 = 84 combinations, it is possible to change the mixing ratio of the combined addition amount.

【0014】タイプ別組合せの一例を上げると、(a)
B系ビスタイプ、(b)長鎖モノタイプの組合せにおい
て、(a)の小さい分子のみの場合と、(b)の長鎖分
子(大きい分子)のみの場合とでは、吸着量に限度があ
り、(a)20〜80vol%、(b)80〜20vo
l%の組合せで、基油(鉱物油、合成油)に添加した場
合、好ましくは、(a)40〜60vol%、(b)6
0〜40vol%を添加した場合、後述するテストで示
すように、各々単独で添加した場合に比べて、次のよう
な効果が認められた。 鉄に対する吸着量が上がる。そしてその結果、 ATFとして処方した時に、高い摩擦係数(μ)を持
つ。
As an example of the combination by type, (a)
In the combination of B type bis type and (b) long chain monotype, there is a limit to the amount of adsorption between the case where only small molecule (a) is used and the case where only long chain molecule (large molecule) of (b) is used. , (A) 20 to 80 vol%, (b) 80 to 20 vo
When added to a base oil (mineral oil, synthetic oil) in a combination of 1%, preferably (a) 40 to 60 vol%, (b) 6
When 0 to 40 vol% was added, as shown in the test described later, the following effects were recognized as compared with the case where each was added alone. The amount of adsorption on iron increases. As a result, it has a high coefficient of friction (μ) when formulated as ATF.

【0015】[0015]

【発明の実施の形態】吸着量測定実験を次の条件で行な
った。 ・添加剤試料をPAO(ポリアルファオレフィン、10
0℃ 4cSt)に、5wt%濃度溶解させ、ビーカー
に約200cc採る。 ・次にSP材(φ20、厚さ2mm)の片面を研磨し
て、仕上げバフ研磨迄施し、鏡面にする。このSP材を
ビーカー中に浸潰して、120℃−96hrs.の条件
で吸着させる。 ・吸着したSP材試料は、取り出して石油ベンジンで表
面を洗浄する。 ・IR−RAS(赤外線高感度反射測定法:Infra
red−Reflection Absorption
Spectroscopy)により、SP材表面に吸
着した添加剤のピーク強度を測定する。
BEST MODE FOR CARRYING OUT THE INVENTION An adsorption amount measurement experiment was conducted under the following conditions. -Additive samples are PAO (polyalphaolefin, 10
Dissolve 5 wt% concentration in 0 ° C. 4 cSt) and collect about 200 cc in a beaker.・ Next, polish one side of SP material (φ20, thickness 2mm) and finish buffing to make it a mirror surface. This SP material was immersed in a beaker and heated at 120 ° C.-96 hrs. Adsorb under the conditions of. -Remove the adsorbed SP material sample and wash the surface with petroleum benzine.・ IR-RAS (Infrared high sensitivity reflection measurement method: Infra
red-Reflection Absorption
The peak intensity of the additive adsorbed on the surface of the SP material is measured by Spectroscopy).

【0016】アルケニルこはく酸イミドのアルケニル基
の平均分子量は、 (a)B系ビスタイプ:平均分子量1000〜1500
程度 (b)長鎖モノタイプ:平均分子量2000〜2500
程度 (c)非B系ビスタイプ:平均分子量1000〜150
0程度とした。比較として用いた超高分子量こはく酸イ
ミド骨格を持つ添加剤の分子量は、 (x)平均分子量5500〜7000 (y)平均分子量55000〜70000 である。
The average molecular weight of the alkenyl group of the alkenyl succinimide is (a) B type bis type: average molecular weight 1000 to 1500
Degree (b) long chain monotype: average molecular weight 2000-2500
(C) Non-B type bis type: average molecular weight 1000-150
It was set to about 0. The molecular weight of the additive having an ultrahigh molecular weight succinimide skeleton used as a comparison is (x) average molecular weight 5500 to 7000 (y) average molecular weight 55000 to 70000.

【0017】図1は吸着量の測定結果を示すグラフであ
り、横軸には(a)B系ビスタイプ:(b)長鎖モノタ
イプ=50%:50%、及び(a)B系ビスタイプ10
0%、(b)長鎖モノタイプ100%を取り、縦軸にピ
ーク強度を取ってある。このグラフから明らかなよう
に、(a)B系ビスタイプ50%と、(b)長鎖モノタ
イプ50%の組合せで、アルケニルこはく酸イミドを用
いた時、上記(a)、(b)を単独で用いた時よりもS
P材(鉄)への吸着量が明らかに多かった。
FIG. 1 is a graph showing the results of measurement of the amount of adsorption. The horizontal axis shows (a) B type bis type: (b) long chain monotype = 50%: 50%, and (a) B type bis. Type 10
0% and (b) long chain monotype 100% are taken, and the vertical axis shows the peak intensity. As is clear from this graph, when alkenyl succinimide is used in a combination of (a) B-based bis type 50% and (b) long-chain monotype 50%, the above (a) and (b) are S more than when used alone
The amount of adsorption to the P material (iron) was obviously high.

【0018】図2はチップオンディスクテストのテスト
結果を示すグラフで、横軸に周速(m/s)、縦軸に摩
擦係数(μ)をとってある。このグラフに示すように、
(a)B系ビスタイプ2.5%、(b)長鎖モノタイプ
2.5%ずつの組合せで添加した場合、(a)、(b)
を夫々5%ずつ単独で用いた時より摩擦係数が大きくな
った。
FIG. 2 is a graph showing the test results of the chip-on-disk test, where the horizontal axis represents the peripheral speed (m / s) and the vertical axis represents the coefficient of friction (μ). As shown in this graph,
When (a) B type bis type 2.5% and (b) long chain monotype 2.5% are added in combination, respectively, (a), (b)
The coefficient of friction was greater than when 5% each was used alone.

【0019】モノタイプとビスタイプでは、構造、極性
基の数(C=0,N)、分子量等が異なり、組合せて添
加することにより、ミセル(凝集体)を作り易く、単位
面積当り高密度に吸着すると考えられる。
The monotype and the bis type differ in structure, number of polar groups (C = 0, N), molecular weight, etc., and when added in combination, micelles (aggregates) are easily formed and high density per unit area is achieved. It is considered to be adsorbed on.

【0020】このテストの結果を基にATFを調整し、
SAE NO.2テストで静摩擦係数(μs)、動摩擦
係数(μd)、及び μ0/μd を測定したところ、
表1、表2、表3に示すようになった。(他の添加剤の
添加量は同一である。) 尚、表1は実施例1〜9の成分表、表2は比較例1〜1
0の成分表、表3は比較例8及び11〜14と実施例1
0〜15の成分表であり、SAE NO.2テスト(ク
ラッチ摩擦試験)でテストした結果を表にしたものであ
る。
Adjust the ATF based on the results of this test,
SAE NO. The static friction coefficient (μs), the dynamic friction coefficient (μd), and μ 0 / μd were measured in 2 tests.
The results are shown in Table 1, Table 2 and Table 3. (The addition amounts of other additives are the same.) In addition, Table 1 is a component table of Examples 1 to 9, and Table 2 is Comparative Examples 1 to 1.
No. 0 component table, Table 3 shows Comparative Examples 8 and 11-14 and Example 1
It is a component table of 0 to 15, and SAE NO. 2 is a table showing the results of the test in the 2 test (clutch friction test).

【0021】[0021]

【表1】 [Table 1]

【0022】基油には下記添加剤を、最大30%添加す
る(30%以上添加しても添加剤のコストに見合う効果
がない)。 (清浄分散剤) アルケニルこはく酸イミド:1〜10% 1%以下では効果は期待できず、10%以上では酸化安
定性が悪く、沈殿、析出する。 (粘度指数向上剤) ポリメタクリレート:4〜20% 4%以下では効果が期待できず、20%以上では溶けに
くい。 (酸化防止剤) アルキルジフェニルアミン:0.5〜4% 0.5%以下では効果が期待できず、4%以上ではオイ
ルを劣化させる。 (摩擦調整剤) アルキルアミン:0.05〜1% 0.05%以下では効果が期待できず、1%以上ではオ
イルを劣化させる。 (極圧剤) SP化合物(市販品「バソルーブ719」、バンダービ
ルト社製):0.1〜4% 0.1%以下では効果が期待できず、4%以上では被毒
性が大きく、耐熱性が悪い。
The following additives are added to the base oil at a maximum of 30% (addition of 30% or more has no effect commensurate with the cost of the additives). (Detergent-dispersing agent) Alkenyl succinimide: 1 to 10% If 1% or less, no effect can be expected, and if 10% or more, oxidative stability is poor and precipitation or precipitation occurs. (Viscosity index improver) Polymethacrylate: 4 to 20% No effect can be expected at 4% or less, and it is difficult to dissolve at 20% or more. (Antioxidant) Alkyldiphenylamine: 0.5 to 4% If 0.5% or less, no effect can be expected, and if 4% or more, oil is deteriorated. (Friction modifier) Alkylamine: 0.05 to 1% If 0.05% or less, no effect can be expected, and if 1% or more, oil is deteriorated. (Extreme pressure agent) SP compound (commercial item "Basolve 719", manufactured by Vanderbilt): 0.1-4% If 0.1% or less, no effect can be expected, and if 4% or more, toxicity is large and heat resistance Is bad.

【0023】基油の動粘度は、100℃で3〜5cS
t。2種以上の鉱油の留分または合成油を組合せたもの
でも良い。粘度指数を上げるためには低粘度の基油を使
う方法もあるが、揮発性で、引火点が低いため、長期の
使用ができない。又、添加剤の配合割合は、実施例に記
載する通りであるが、1つの添加剤の配合量が決まれ
ば、他の添加剤の配合量も該割合で決まり、潤滑剤の系
のバランスがとれる。
The kinematic viscosity of the base oil is 3 to 5 cS at 100 ° C.
t. A combination of two or more kinds of mineral oil fractions or synthetic oils may be used. Although there is a method of using a low-viscosity base oil to increase the viscosity index, it cannot be used for a long time because it is volatile and has a low flash point. Further, the blending ratio of the additives is as described in the examples, but once the blending amount of one additive is determined, the blending amount of the other additives is also determined by the proportion, and the balance of the lubricant system is Can be taken.

【0024】(実施例1):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.5wt%:2.5wt%=50wt%:50wt%
で配合。尚、比例式の前半は基油に対する割合、後半は
2つのアルケニルこはく酸イミドの割合である。以下同
様である。
(Example 1): Alkenyl succinimide, (a) B type bis type: (b) long chain monotype =
2.5 wt%: 2.5 wt% = 50 wt%: 50 wt%
Blended with. The first half of the proportional formula is the ratio to the base oil, and the second half is the ratio of the two alkenyl succinimides. The same applies hereinafter.

【0025】(実施例2):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
3.0wt%:2.0wt%=60wt%:40wt%
で配合。
(Example 2): Alkenyl succinimide, (a) B type bis type: (b) long chain monotype =
3.0 wt%: 2.0 wt% = 60 wt%: 40 wt%
Blended with.

【0026】(実施例3):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.0wt%:3.0wt%=40wt%:60wt%
で配合。
(Example 3): Alkenyl succinimide (a) B type bis type: (b) long chain monotype =
2.0 wt%: 3.0 wt% = 40 wt%: 60 wt%
Blended with.

【0027】(実施例4):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
3.5wt%:1.5wt%=70wt%:30wt%
で配合。
(Example 4): Alkenyl succinimide (a) B type bis type: (b) long chain monotype =
3.5 wt%: 1.5 wt% = 70 wt%: 30 wt%
Blended with.

【0028】(実施例5):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
1.5wt%:3.5wt%=30wt%:70wt%
で配合。
(Example 5): Alkenyl succinimide (a) B type bis type: (b) long chain monotype =
1.5 wt%: 3.5 wt% = 30 wt%: 70 wt%
Blended with.

【0029】(実施例6):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ:
(c)非B系ビスタイプ=2.5wt%:1.25wt
%:1.25wt%=50wt%:25wt%:25w
t%で配合。
(Example 6): Alkenyl succinimide, (a) B type bis type: (b) long chain monotype:
(C) Non-B type bis type = 2.5 wt%: 1.25 wt
%: 1.25 wt% = 50 wt%: 25 wt%: 25w
Blended at t%.

【0030】(実施例7):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.5wt%:2.5wt%=50wt%:50wt%
で配合。又、アルキルアミンの基油に対する割合は、
0.2wt%である。
(Example 7) Alkenyl succinimide was used as (a) B type bis type: (b) long chain monotype =
2.5 wt%: 2.5 wt% = 50 wt%: 50 wt%
Blended with. The ratio of alkylamine to base oil is
It is 0.2 wt%.

【0031】(実施例8):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.5wt%:2.5wt%=50wt%:50wt%
で配合。又、アルキルアミンの基油に対する割合は、
0.1wt%である。
(Example 8): Alkenyl succinimide (a) B type bis type: (b) long chain monotype =
2.5 wt%: 2.5 wt% = 50 wt%: 50 wt%
Blended with. The ratio of alkylamine to base oil is
It is 0.1 wt%.

【0032】(実施例9):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.5wt%:2.5wt%=50wt%:50wt%
で配合。又、アルキルアミンの基油に対する割合は、
1.0wt%である。
(Example 9) Alkenyl succinimide was used as (a) B type bis type: (b) long chain monotype =
2.5 wt%: 2.5 wt% = 50 wt%: 50 wt%
Blended with. The ratio of alkylamine to base oil is
It is 1.0 wt%.

【0033】[0033]

【表2】 [Table 2]

【0034】実施例において、ポリジメチルシロキサン
の配合範囲は、10ppm〜100ppm。10ppm
以下の場合、摩擦係数の向上は期待できず、100pp
m以上では分散できない。
In the examples, the compounding range of polydimethylsiloxane is 10 ppm to 100 ppm. 10 ppm
In the following cases, improvement of friction coefficient cannot be expected and 100pp
If it is more than m, it cannot be dispersed.

【0035】実施例において、摩擦係数が向上し、粘度
指数が向上するのは、ポリジメチルシロキサンがビスタ
イプと、モノタイプの配置を均一にするので、鉄に対す
る吸着が緻密になり、吸着量が増大するためと思われ
る。又、ポリジメチルシロキサンは、ATFが機械的に
攪拌された時に生じる油中の気泡を抑制すると共に、ビ
スタイプとモノタイプの分散、及び金属に対する吸着を
助長していると考えられる。特に高分子量(動粘度50
00〜20000cSt)(25℃)のポリジメチルシ
ロキサンと、低分子量(動粘度10〜100cSt)
(25℃)のポリジメチルシロキサンを4:1〜1:4
の割合で混合した時に、上記吸着が助長されるものと考
えられる。
In the examples, the friction coefficient and the viscosity index are improved because the polydimethylsiloxane makes the bis type and the mono type arranged uniformly, so that the adsorption on iron is dense and the adsorption amount is high. It seems to increase. Further, it is considered that the polydimethylsiloxane suppresses air bubbles in the oil generated when the ATF is mechanically stirred, and promotes dispersion of bis type and mono type and adsorption of metal. Especially high molecular weight (kinematic viscosity 50
Polydimethylsiloxane (00 to 20000 cSt) (25 ° C) and low molecular weight (kinematic viscosity 10 to 100 cSt)
(25 ° C) polydimethylsiloxane 4: 1 to 1: 4
It is considered that the above adsorption is promoted when mixed at a ratio of.

【0036】ポリジメチルシロキサンが存在しない場
合、十分な分散、吸着が実現しない。消泡効果が不
足し、油膜切れ等により非接触部の割合が増し、ATF
の摩擦係数の向上が妨げられる。以上の理由により、A
TFの摩擦係数を向上させる上でマイナスの影響を及ぼ
すと考えられる。
In the absence of polydimethylsiloxane, sufficient dispersion and adsorption cannot be realized. The defoaming effect is insufficient, and the ratio of non-contact parts increases due to oil film breakage, etc.
The improvement of the friction coefficient of is hindered. For the above reasons, A
It is considered to have a negative influence on improving the friction coefficient of TF.

【0037】(比較例1):アルケニルこはく酸イミド
を、(a)B系ビスタイプ5.0wt%配合し、(b)
長鎖モノタイプは配合しない。
(Comparative Example 1): Alkenyl succinimide was added to (a) B type bis type of 5.0 wt%, and (b).
Do not mix long chain monotype.

【0038】(比較例2):アルケニルこはく酸イミド
を、(b)長鎖モノタイプ5.0wt%配合し、(a)
B系ビスタイプは配合しない。
(Comparative Example 2): Alkenyl succinimide was blended with (b) 5.0 wt% of long-chain monotype, (a)
B type bis type is not mixed.

【0039】(比較例3):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
0.5wt%:4.5wt%=10wt%:90wt%
で配合。
(Comparative Example 3): Alkenyl succinimide (a) B type bis type: (b) long chain monotype =
0.5 wt%: 4.5 wt% = 10 wt%: 90 wt%
Blended with.

【0040】(比較例4):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
4.5wt%:0.5wt%=90wt%:10wt%
で配合。
(Comparative Example 4): Alkenyl succinimide (a) B type bis type: (b) long chain monotype =
4.5 wt%: 0.5 wt% = 90 wt%: 10 wt%
Blended with.

【0041】(比較例5):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
1.0wt%:4.0wt%=20wt%:80wt%
で配合。
(Comparative Example 5): Alkenyl succinimide (a) B type bis type: (b) long chain monotype =
1.0 wt%: 4.0 wt% = 20 wt%: 80 wt%
Blended with.

【0042】(比較例6):アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
4.0wt%:1.0wt%=80wt%:20wt%
で配合。
(Comparative Example 6): Alkenyl succinimide was used as (a) B type bis type: (b) long chain monotype =
4.0 wt%: 1.0 wt% = 80 wt%: 20 wt%
Blended with.

【0043】(比較例7):超高分子量アルケニルこは
く酸イミドを、(x)B系ビスタイプ:(y)長鎖モノ
タイプ=2.5wt%:2.5wt%=50wt%:5
0wt%で配合。又、ポリメタクリレートの基油に対す
る割合は、4.0wt%である。
(Comparative Example 7): Ultra high molecular weight alkenyl succinimide, (x) B type bis type: (y) long chain monotype = 2.5 wt%: 2.5 wt% = 50 wt%: 5
Blended with 0 wt%. The ratio of polymethacrylate to the base oil is 4.0 wt%.

【0044】(比較例8):超高分子量アルケニルこは
く酸イミドを、(x)B系ビスタイプ:(y)長鎖モノ
タイプ=2.5wt%:2.5wt%=50wt%:5
0wt%で配合。
(Comparative Example 8): Ultra high molecular weight alkenyl succinimide, (x) B type bis type: (y) long chain monotype = 2.5 wt%: 2.5 wt% = 50 wt%: 5
Blended with 0 wt%.

【0045】(比較例9)アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.5wt%:2.5wt%=50wt%:50wt%
で配合。又、アルキルアミンの基油に対する割合は、
0.01wt%である。
(Comparative Example 9) Alkenyl succinimide was added to (a) B type bis type: (b) long chain monotype =
2.5 wt%: 2.5 wt% = 50 wt%: 50 wt%
Blended with. The ratio of alkylamine to base oil is
It is 0.01 wt%.

【0046】[0046]

【表3】 [Table 3]

【0047】ポリジメチルシロキサンの高分子量のもの
と、低分子量のものとを組合せて用いると、こはく酸イ
ミドのモノタイプとビスタイプの組合せで生じた吸着が
更に助長され、摩擦係数が向上したと考えられる。
When a high molecular weight polydimethylsiloxane and a low molecular weight polydimethylsiloxane are used in combination, the adsorption generated by the combination of succinimide monotype and bistype is further promoted, and the friction coefficient is improved. Conceivable.

【0048】トリラウリルトリチオフォスフェートを少
量添加して、こはく酸イミドのモノタイプと、ビスタイ
プの組合せと共に、ATFを処方すると、摩擦係数が向
上することが判った。これは、こはく酸イミドの組合せ
により得た吸着による摩擦係数を向上させる効果を、よ
り一層補完する効果が発揮されるものと考えられる。
It has been found that when ATF is formulated with a combination of succinimide monotype and bis type with the addition of a small amount of trilauryl trithiophosphate, the coefficient of friction is improved. This is considered to exert the effect of further complementing the effect of improving the friction coefficient by adsorption obtained by the combination of succinimide.

【0049】(実施例10):超高分子量アルケニルこ
はく酸イミドを(x)B系ビスタイプ:(y)長鎖モノ
タイプ=2.5wt%:2.5wt%=50wt%:5
0wt%で配合。又、トリラウリルトリチオフォスフェ
ートを基油に対して0.01wt%配合する。ポリジメ
チルシロキサンは、低分子量のものを25ppm、高分
子量のものを25ppm配合する。
(Example 10): Ultra high molecular weight alkenyl succinimide (x) B type bis type: (y) long chain monotype = 2.5 wt%: 2.5 wt% = 50 wt%: 5
Blended with 0 wt%. Further, trilauryl trithiophosphate is blended in an amount of 0.01 wt% with respect to the base oil. As for polydimethylsiloxane, 25 ppm of low molecular weight and 25 ppm of high molecular weight are blended.

【0050】(実施例11):超高分子量アルケニルこ
はく酸イミドを(x)B系ビスタイプ:(y)長鎖モノ
タイプ=2.5wt%:2.5wt%=50wt%:5
0wt%で配合。又、トリラウリルトリチオフォスフェ
ートを、基油に対して0.01wt%配合する。
(Example 11): Ultra high molecular weight alkenyl succinimide (x) B type bis type: (y) long chain monotype = 2.5 wt%: 2.5 wt% = 50 wt%: 5
Blended with 0 wt%. Also, trilauryl trithiophosphate is blended in an amount of 0.01 wt% with respect to the base oil.

【0051】(実施例12):アルケニルこはく酸イミ
ドを、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.5wt%:2.5wt%=50wt%:50wt%
で配合。又、ポリジメチルシロキサンは、低分子量のも
のを25ppm、高分子量のものを25ppm配合す
る。
(Example 12) Alkenyl succinimide was used as (a) B-based bis type: (b) long-chain monotype =
2.5 wt%: 2.5 wt% = 50 wt%: 50 wt%
Blended with. The polydimethylsiloxane is blended with 25 ppm of low molecular weight and 25 ppm of high molecular weight.

【0052】(実施例13):アルケニルこはく酸イミ
ドを、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.5wt%:2.5wt%=50wt%:50wt%
で配合。又、トリラウリルトリチオフォスフェートを、
基油に対して0.01wt%配合する。
(Example 13) Alkenyl succinimide was used as (a) B type bis type: (b) long chain monotype =
2.5 wt%: 2.5 wt% = 50 wt%: 50 wt%
Blended with. Also, trilauryl trithiophosphate,
Add 0.01 wt% to the base oil.

【0053】(実施例14)アルケニルこはく酸イミド
を、(a)B系ビスタイプ:(b)長鎖モノタイプ=
2.5wt%:2.5wt%=50wt%:50wt%
で配合。又、ポリジメチルシロキサンは、低分子量のも
のを25ppm、高分子量のものを25ppm配合す
る。
(Example 14) Alkenyl succinimide was used as (a) B type bis type: (b) long chain monotype =
2.5 wt%: 2.5 wt% = 50 wt%: 50 wt%
Blended with. The polydimethylsiloxane is blended with 25 ppm of low molecular weight and 25 ppm of high molecular weight.

【0054】(実施例15)超高分子量アルケニルこは
く酸イミドを(x)B系ビスタイプ:(y)長鎖モノタ
イプ=2.5wt%:2.5wt%=50wt%:50
wt%で配合。又、ポリジメチルシロキサンは、低分子
量のものを25ppm、高分子量のものを25ppm配
合する。
(Example 15) Ultra high molecular weight alkenyl succinimide (x) B type bis type: (y) long chain mono type = 2.5 wt%: 2.5 wt% = 50 wt%: 50
Blended in wt%. The polydimethylsiloxane is blended with 25 ppm of low molecular weight and 25 ppm of high molecular weight.

【0055】(比較例10):超高分子アルケニルこは
く酸イミドを(x)B系ビスタイプ5.0wt%配合
し、(b)長鎖モノタイプは配合しない。又、ポリジメ
チルシロキサンは、低分子量のものを25ppm、高分
子量のものを25ppm配合する。
(Comparative Example 10): Ultra high molecular weight alkenyl succinimide (x) 5.0 wt% of B type bis type was compounded, and (b) long chain monotype was not compounded. The polydimethylsiloxane is blended with 25 ppm of low molecular weight and 25 ppm of high molecular weight.

【0056】(比較例11):超高分子アルケニルこは
く酸イミドを(x)B系ビスタイプ5.0wt%配合
し、(b)長鎖モノタイプは配合しない。又、トリラウ
リルトリチオフォスフェートを、基油に対して0.01
wt%配合する。
(Comparative Example 11): 5.0% by weight of (x) B-based bis type alkenyl succinimide was blended and (b) long chain monotype was not blended. Also, trilauryl trithiophosphate was added to the base oil at 0.01
wt% is added.

【0057】(比較例12):アルケニルこはく酸イミ
ドを、(a)B系ビスタイプ5.0wt%配合し、
(b)長鎖モノタイプは配合しない。又、ポリジメチル
シロキサンは、低分子量のものを25ppm、高分子量
のものを25ppm配合する。
(Comparative Example 12): (a) B-based bis type of 5.0 wt% was blended with alkenyl succinimide,
(B) Long chain monotype is not mixed. The polydimethylsiloxane is blended with 25 ppm of low molecular weight and 25 ppm of high molecular weight.

【0058】(比較例13)アルケニルこはく酸イミド
を、(a)B系ビスタイプ5.0wt%配合し、(b)
長鎖モノタイプは配合しない。又、トリラウリルトリチ
オフォスフェートを、基油に対して0.01wt%配合
する。
(Comparative Example 13) Alkenyl succinimide was mixed in (a) B type bis type of 5.0 wt%, and (b)
Do not mix long chain monotype. Also, trilauryl trithiophosphate is blended in an amount of 0.01 wt% with respect to the base oil.

【0059】図3は表1、表2のアルケニルこはく酸イ
ミドの配合量の変化による静摩擦係数の推移を示すグラ
フ、図4は同じくアルケニルこはく酸イミドの配合量
(重量%)の変化による動摩擦係数の推移を示すグラフ
である。
FIG. 3 is a graph showing the change of the static friction coefficient depending on the change of the blending amount of alkenyl succinimide in Tables 1 and 2, and FIG. 4 is the dynamic friction coefficient depending on the change of the blending amount (wt%) of alkenyl succinimide. It is a graph which shows the change of.

【0060】この図3、図4から明らかなように、アル
ケニルこはく酸イミドの吸着量がATFの高μ化を左右
することが判り、実用上アルケニルこはく酸イミドの
(a)B系ビスタイプと、(b)長鎖モノタイプを20
wt%〜80wt%の割合で配合した時、好ましくは3
0wt%〜70wt%の割合で配合した時、高い静摩擦
係数(μs)、及び動摩擦係数(μd)を得ることが出
来る。
As is clear from FIGS. 3 and 4, it was found that the amount of alkenyl succinimide adsorbed affects the increase in ATF μ. , (B) 20 long chain monotypes
When blended in a ratio of from wt% to 80 wt%, preferably 3
When blended in a proportion of 0 wt% to 70 wt%, a high static friction coefficient (μs) and high dynamic friction coefficient (μd) can be obtained.

【0061】そしてこの時、図1、図2で説明したよう
に、(a)B系ビスタイプが平均分子量1000〜15
00程度、(b)長鎖モノタイプが平均分子量2000
〜2500程度になっている。
At this time, as described with reference to FIGS. 1 and 2, (a) B type bis type has an average molecular weight of 1000 to 15
00, (b) long chain monotype has an average molecular weight of 2000
It is about 2,500.

【0062】[0062]

【発明の効果】以上詳述したように本発明によれば、次
のような効果を奏する。請求項1によれば、基油に、ビ
スタイプ及びモノタイプの2種のアルケニルこはく酸イ
ミドと、ポリジメチルシロキサンの動粘度10〜100
cStの低分子量物と動粘度5000〜20000cS
tの高分子量物の組合せた添加剤を配合したので、吸着
量が制御され、摩擦係数を向上させることが出来る。
As described in detail above, the present invention has the following effects. According to claim 1, two types of alkenyl succinimide of bis type and mono type are added to the base oil, and kinematic viscosity of polydimethylsiloxane is 10 to 100.
Low molecular weight cSt and kinematic viscosity 5000 to 20000 cS
Since the additive in which the high molecular weight substance of t is combined is blended, the adsorption amount is controlled, and the friction coefficient can be improved.

【0063】請求項2によれば、基油に、ビスタイプ及
びモノタイプの2種のアルケニルこはく酸イミドと、ト
リラウリルチオフォスフェートを組合せた添加剤を配合
したので、静摩擦係数と動摩擦係数を向上させることが
できる。
According to the second aspect of the present invention, since the base oil is blended with the additive which is a combination of two types of alkenyl succinimide of bis type and mono type and trilauryl thiophosphate, the static friction coefficient and the dynamic friction coefficient are improved. Can be made.

【0064】請求項3によれば、基油に、アルケニル基
の平均分子量が1000〜1500と、2000〜25
00の2種のアルケニルこはく酸イミドの添加剤を配合
したので、摩擦係数を向上させることが出来る。
According to claim 3, the base oil has an alkenyl group having an average molecular weight of 1,000 to 1,500 and 2,000 to 25.
Since two kinds of alkenyl succinimide additives of No. 00 are mixed, the friction coefficient can be improved.

【0065】請求項4によれば、100℃の動粘度が3
cSt以上の基油に、アルケニル基の平均分子量が10
00〜1500と、2000〜2500の2種のアルケ
ニルこはく酸イミドの添加剤を配合したので、粘度指数
を向上させて、静摩擦係数と動摩擦係数を向上させるこ
とができる。
According to claim 4, the kinematic viscosity at 100 ° C. is 3
The average molecular weight of the alkenyl group is 10 in base oil of cSt or more
Since two kinds of alkenyl succinimide additives of 00 to 1500 and 2000 to 2500 are mixed, the viscosity index can be improved and the static friction coefficient and the dynamic friction coefficient can be improved.

【図面の簡単な説明】[Brief description of drawings]

【図1】吸着量の測定結果を示すグラフFIG. 1 is a graph showing a measurement result of an adsorption amount.

【図2】チップオンディスクテストの結果を示すグラフFIG. 2 is a graph showing the results of a chip-on-disk test.

【図3】アルケニルこはく酸イミドの配合量(重量%)
の変化による静摩擦係数の推移を示すグラフ
[Fig. 3] Blend amount of alkenyl succinimide (% by weight)
Graph showing changes in static friction coefficient due to changes in

【図4】アルケニルこはく酸イミドの配合量(重量%)
の変化による動摩擦係数の推移を示すグラフ
FIG. 4 Blending amount of alkenyl succinimide (% by weight)
Graph showing changes in dynamic friction coefficient due to changes in

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C10M 137:10) Z C10N 20:04 30:04 30:06 40:04 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display location C10M 137: 10) Z C10N 20:04 30:04 30:06 40:04

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 基油に下記添加剤、 ビスタイプ及びモノタイプの2種のアルケニルこはく酸
イミドと、 ポリジメチルシロキサンの動粘度10〜100cStの
低分子量物と動粘度5000〜20000cStの高分
子量物、 を組合せて配合した潤滑油組成物。
1. A base oil containing the following additives, two alkenyl succinimides of bis type and mono type, a low molecular weight substance having a kinematic viscosity of 10 to 100 cSt and a high molecular weight substance having a kinematic viscosity of 5,000 to 20,000 cSt. A lubricating oil composition prepared by combining and
【請求項2】 基油に下記添加剤、 ビスタイプ及びモノタイプの2種のアルケニルこはく酸
イミドと、 トリラウリルチオフォスフェート、 を組合せて配合した潤滑油組成物。
2. A lubricating oil composition prepared by combining a base oil with the following additives, two alkenyl succinimides of bis type and mono type, and trilauryl thiophosphate.
【請求項3】 基油に下記添加剤、 アルケニル基の平均分子量が1000〜1500と、2
000〜2500の2種のアルケニルこはく酸イミドを
配合した潤滑油組成物。
3. The following additives to the base oil, wherein the alkenyl group has an average molecular weight of 1000 to 1500 and 2.
A lubricating oil composition containing 000 to 2500 alkenyl succinimide.
【請求項4】 100℃の動粘度が3cSt以上の基油
に下記添加剤、 アルケニル基の平均分子量が1000〜1500と、2
000〜2500の2種のアルケニルこはく酸イミドを
配合した潤滑油組成物。
4. A base oil having a kinematic viscosity at 100 ° C. of 3 cSt or more and the following additives, and the alkenyl group having an average molecular weight of 1000 to 1500:
A lubricating oil composition containing 000 to 2500 alkenyl succinimide.
JP7214565A 1994-09-05 1995-08-23 Lubricating oil composition Expired - Fee Related JP2842585B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP7214565A JP2842585B2 (en) 1994-09-05 1995-08-23 Lubricating oil composition
DE69513588T DE69513588T2 (en) 1994-09-05 1995-09-05 Lubricant composition
EP95113919A EP0699738B1 (en) 1994-09-05 1995-09-05 Lubricant composition

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP6-211602 1994-09-05
JP21160294 1994-09-05
JP7214565A JP2842585B2 (en) 1994-09-05 1995-08-23 Lubricating oil composition

Publications (2)

Publication Number Publication Date
JPH08127789A true JPH08127789A (en) 1996-05-21
JP2842585B2 JP2842585B2 (en) 1999-01-06

Family

ID=26518736

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Country Status (3)

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EP (1) EP0699738B1 (en)
JP (1) JP2842585B2 (en)
DE (1) DE69513588T2 (en)

Cited By (5)

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JP2000345181A (en) * 1999-06-04 2000-12-12 Idemitsu Kosan Co Ltd Fluid for traction drive
JP2004155873A (en) * 2002-11-05 2004-06-03 Nippon Oil Corp Lubricating oil composition
WO2007088649A1 (en) * 2006-01-31 2007-08-09 Nissan Motor Co., Ltd. Nanoparticle-containing lubricating oil compositions
JP2008120889A (en) * 2006-11-10 2008-05-29 Showa Shell Sekiyu Kk Lubricating oil composition
JP2014125527A (en) * 2012-12-26 2014-07-07 Showa Shell Sekiyu Kk Method for improving the flash point of oil or oil composition and flash point-improved oily composition

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3520198B2 (en) 1998-05-08 2004-04-19 東燃ゼネラル石油株式会社 Lubricating oil composition
US7553429B2 (en) 2005-08-04 2009-06-30 Ashland Licensing And Intellectual Property, Llc Traction fluid composition
CN102784983A (en) * 2011-05-20 2012-11-21 昆山市瑞捷精密模具有限公司 Working solution for high-speed wire electrical discharge machining

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59122597A (en) * 1982-11-30 1984-07-16 Honda Motor Co Ltd Lubricating oil composition

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000345181A (en) * 1999-06-04 2000-12-12 Idemitsu Kosan Co Ltd Fluid for traction drive
JP2004155873A (en) * 2002-11-05 2004-06-03 Nippon Oil Corp Lubricating oil composition
JP4571776B2 (en) * 2002-11-05 2010-10-27 Jx日鉱日石エネルギー株式会社 Lubricating oil composition
WO2007088649A1 (en) * 2006-01-31 2007-08-09 Nissan Motor Co., Ltd. Nanoparticle-containing lubricating oil compositions
US9023771B2 (en) 2006-01-31 2015-05-05 Nissan Motor Co., Ltd. Nanoparticle-containing lubricating oil compositions
JP2008120889A (en) * 2006-11-10 2008-05-29 Showa Shell Sekiyu Kk Lubricating oil composition
JP2014125527A (en) * 2012-12-26 2014-07-07 Showa Shell Sekiyu Kk Method for improving the flash point of oil or oil composition and flash point-improved oily composition

Also Published As

Publication number Publication date
DE69513588D1 (en) 2000-01-05
DE69513588T2 (en) 2000-03-30
EP0699738A1 (en) 1996-03-06
EP0699738B1 (en) 1999-12-01
JP2842585B2 (en) 1999-01-06

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