JP2000109876A - Hydraulic oil composition for buffer - Google Patents

Hydraulic oil composition for buffer

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Publication number
JP2000109876A
JP2000109876A JP10287958A JP28795898A JP2000109876A JP 2000109876 A JP2000109876 A JP 2000109876A JP 10287958 A JP10287958 A JP 10287958A JP 28795898 A JP28795898 A JP 28795898A JP 2000109876 A JP2000109876 A JP 2000109876A
Authority
JP
Japan
Prior art keywords
viscosity
oil
mineral oil
low
shock absorber
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP10287958A
Other languages
Japanese (ja)
Inventor
Eiji Kamata
栄司 鎌田
Hiroshi Ohashi
広 大橋
Naoto Otsuka
直登 大塚
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.)
Tonen General Sekiyu KK
Original Assignee
Tonen Corp
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Filing date
Publication date
Application filed by Tonen Corp filed Critical Tonen Corp
Priority to JP10287958A priority Critical patent/JP2000109876A/en
Priority to SG9904835A priority patent/SG108213A1/en
Priority to CA002284343A priority patent/CA2284343A1/en
Priority to EP99307976A priority patent/EP0992570A3/en
Publication of JP2000109876A publication Critical patent/JP2000109876A/en
Priority to US10/682,545 priority patent/US7078391B2/en
Pending legal-status Critical Current

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    • C10M111/02Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a non-macromolecular organic compound
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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
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  • Lubricants (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a hydraulic oil compsn, for buffers, which is excellent in low-temp. viscosity characteristics, vaporizability, and shear stability and has a stable damping power at from low to high temps. SOLUTION: This compsn. contains, based on the compsn., at least 80 wt.% base oil comprising (A)(a) a deeply dewaxed mineral oil or a mixed mineral oil consisting of (a) a deeply dewaxed mineral oil and (b) a low-viscosity mineral oil in a wt. ratio of (80/20)-(100/0) or comprising (B) a synthetic base oil consisting of at least either (c) a poly-α-olefin or (d) an ester compd., is prepd. by compounding the base oil with (C) 20 wt.% or lower additive comprising (e) a viscosity index improver and/or a flow point depressant, and has a kinematic viscosity of 1-20 mm2/s at 100 deg.C, a viscosity index of 140 or higher, and a Brookfield viscosity of 29 000 mPa.s or lower at -40 deg.C.

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、緩衝器用油圧作動
油組成物に関する。さらに詳しくは、減衰力安定性に優
れた、特に低温での乗り心地がよい緩衝器用油圧作動油
組成物に関するものである。
TECHNICAL FIELD The present invention relates to a hydraulic oil composition for a shock absorber. More specifically, the present invention relates to a hydraulic fluid composition for a shock absorber having excellent damping force stability, and particularly having good riding comfort at low temperatures.

【0002】[0002]

【従来の技術】自動車における車体のサスペンション
(懸架装置)に、振動を緩和して乗り心地や操縦安定性
の向上のために、一般に油圧型のショックアブソーバー
(緩衝器)が使用されている。緩衝器の構造は、オイル
の流動抵抗を利用した筒形構造が基本となっており、通
常は、油圧のピストンに小さな孔を開けたものが使用さ
れる。この筒形構造を有する緩衝器では、ピストンの上
下に応じて油が孔を通過するが、その時の抵抗はピスト
ンのスピードに比例する。そのため、シリンダーとピス
トンロッドとの摺動部分には、互いの摩耗を防ぐために
案内を兼ねたガイドブッシュが入れられており、更にオ
イル漏れを防ぐため全体がシールされている。また、緩
衝器としては、上記した筒形構造のもの以外に、二重管
型やガス入り型など各種のものが知られている。このよ
うな構造をした緩衝器の場合、前記した如く、ピストン
ロッドとガイドブッシュの間、ピストンロッドとシール
の間、ピストンとシリンダーの間などに多数の複合した
摩擦が発生する。その上、自動車の場合、厳しい走行条
件下において自動車への振動を緩和して乗り心地や操縦
安定性を確保することが必要であり、そのため、従来、
緩衝器に使用される油圧作動油に対し、耐摩耗性が良好
で耐久性があるとともに、摩擦特性が良好であることが
求められている。自動車では、この他、同様の緩衝器が
エンジンの支持装置、バンパーの衝撃吸収装置、ドアチ
ェッカー等にも使用されている。また、航空機でも、離
着陸時の衝撃吸収のための油圧型の緩衝器が配置されて
いる。これらの緩衝器に使用される油圧作動油について
も、前記と同様の性能が求められている。
2. Description of the Related Art In general, a hydraulic shock absorber (buffer) is used for a suspension (suspension device) of a vehicle body of an automobile in order to reduce vibration and improve ride comfort and steering stability. The structure of the shock absorber is basically a cylindrical structure using the flow resistance of oil, and usually a hydraulic piston having a small hole in a piston is used. In the shock absorber having this cylindrical structure, oil passes through the hole according to the up and down of the piston, and the resistance at that time is proportional to the speed of the piston. For this reason, a guide bush, which also serves as a guide, is provided in the sliding portion between the cylinder and the piston rod to prevent mutual wear, and the whole is sealed to prevent oil leakage. Various types of shock absorbers, such as a double-tube type and a gas-filled type, are known in addition to the above-mentioned cylindrical structure. In the case of the shock absorber having such a structure, as described above, a large number of combined frictions occur between the piston rod and the guide bush, between the piston rod and the seal, between the piston and the cylinder, and the like. In addition, in the case of a car, it is necessary to reduce the vibration to the car under severe driving conditions to ensure ride comfort and steering stability.
It is required that the hydraulic oil used for the shock absorber has good wear resistance and durability, and good friction characteristics. In automobiles, similar shock absorbers are also used in engine support devices, bumper shock absorbers, door checkers, and the like. Also, in an aircraft, a hydraulic shock absorber for absorbing impact during takeoff and landing is arranged. The same performance as described above is required for the hydraulic oil used in these shock absorbers.

【0003】従来、良好な耐摩耗性、耐久性及び摩擦特
性を有する緩衝器用油圧作動油としては、潤滑油基油中
にジチオりん酸亜鉛(Zn−DTP)を長鎖脂肪酸など
の油性剤や清浄分散剤と共に添加した緩衝器用油圧作動
油組成物(特開昭55−165996号公報)、潤滑油
基油にホウ素含有清浄分散剤とりん酸エステルを含有さ
せた緩衝器用流体組成物(特公平2−44879号公
報)、潤滑油基油にりん酸エステル等とアルカノールア
ミンを含有させた緩衝器用油圧作動油組成物(特開平5
−255683号公報)、潤滑油基油にリン酸エステル
等と脂肪族ポリアミンを配合した緩衝器用油圧作動油組
成物(特開平7−224293号公報)、及び潤滑油基
油にリン酸エステル等と脂肪族ポリアミン、脂肪族モノ
アミンを配合した緩衝器用油圧作動油組成物(特開平7
−258673号公報)などが提案されている。
[0003] Conventionally, as a hydraulic fluid for a shock absorber having good wear resistance, durability and friction characteristics, zinc dithiophosphate (Zn-DTP) in a lubricating base oil has been used as an oily agent such as a long-chain fatty acid. Hydraulic hydraulic oil composition for buffer added together with detergent dispersant (Japanese Patent Application Laid-Open No. 55-165996), and fluid composition for buffer containing lubricant base oil containing boron-containing detergent dispersant and phosphate ester JP-A-2-44879), a hydraulic oil composition for a buffer containing a phosphate ester or the like and an alkanolamine in a lubricating base oil (Japanese Patent Application Laid-Open No. HEI 5 (1993) -205).
JP-A-255683), a hydraulic fluid composition for a shock absorber in which a phosphate ester or the like and an aliphatic polyamine are blended in a lubricating base oil (JP-A-7-224293), and a phosphate ester or the like in the lubricating base oil. Hydraulic hydraulic oil composition for a shock absorber containing an aliphatic polyamine and an aliphatic monoamine
No. 258,673).

【0004】ところで、緩衝器は、制振作用を行うもの
であるが、制振力を普通、減衰力と呼び、緩衝器の性能
は、作動速度と減衰力に関係する。緩衝器、特に自動車
用緩衝器の場合、厳しい走行条件下において自動車への
振動を緩和して乗り心地や操縦安定性を確保することが
必要であるために、減衰力を安定して保持することが最
重要である。減衰力は、液体、すなわち油圧作動油の流
動抵抗と緩衝器各摺動部の摩擦力等が関与しており、複
数の抵抗の組み合わせである。したがって減衰力を一定
範囲に保持するためには、使用する油圧作動油の粘度と
摩擦特性ができるだけ安定していることが必要となる。
しかしながら、従来から提案されている緩衝器用油圧作
動油は、上記に示す如く、耐摩耗性や摩擦特性に関する
ものが殆どであり、粘度特性に関したものは少なく、例
えば、40℃における動粘度が3〜500cSt、流動
点が−25℃以下、かつくもり点が−25℃以下である
深脱ロウ基油に、粘度指数向上剤やリン系極圧剤を配合
したオリフィス機構を有する機械装置用潤滑油組成物
(特開昭63−280797号公報)などがあるのみで
ある。
By the way, the shock absorber performs a vibration damping action, and the damping force is usually called a damping force, and the performance of the shock absorber is related to the operating speed and the damping force. In the case of shock absorbers, especially automobile shock absorbers, it is necessary to reduce the vibration to the car under severe driving conditions to ensure ride comfort and steering stability, so that the damping force should be stably maintained. Is the most important. The damping force is related to the flow resistance of the liquid, that is, the hydraulic oil, the frictional force of each sliding portion of the shock absorber, and the like, and is a combination of a plurality of resistances. Therefore, in order to keep the damping force within a certain range, it is necessary that the viscosity and friction characteristics of the hydraulic oil used are as stable as possible.
However, most of conventionally proposed hydraulic fluids for shock absorbers are related to abrasion resistance and friction characteristics, and few are related to viscosity characteristics. Lubricating oil for machine equipment having an orifice mechanism in which a viscosity index improver or a phosphorus-based extreme pressure agent is blended with a deeply dewaxed base oil having a pour point of -25 ° C or less and a cloud point of -25 ° C or less. There is only a composition (JP-A-63-280797).

【0005】緩衝器は、比較的広い温度範囲で使用され
るために、温度による粘度の変化を小さくし、減衰力の
変化を招かなくする必要がある。特に、緩衝器用油圧作
動油の粘度は、低温になると増加し、低温粘度が高くな
り過ぎると、減衰力が大きくなりスムースな作動ができ
なくなって、乗り心地や操縦安定性が悪化する。そのた
めに、最近では、低温での減衰力の維持についての要求
が厳しくなっており、例えば、−20℃〜−40℃まで
の低温での減衰力を大幅に低減することが要求されてお
り、そのために緩衝器用油圧作動油に対して、低温粘度
特性の良いものが強く望まれている。しかしながら、従
来からの緩衝器用油圧作動油は、低粘度の基油に粘度指
数向上剤や流動点降下剤を配合しているが、低温粘度を
良くするために、基油粘度を下げると揮発性が増し、蒸
発量の増加やキャビテーションによる減衰力の変動を招
くという欠点を有している。さらに、粘度指数向上剤や
流動点降下剤を多量に配合した緩衝器用油圧作動油は、
ピストンの摺動やオリフィス内を油が流動する際に、剪
断を受け、その緩衝器用油圧作動油の粘度が低下する。
粘度の大幅な低下は、減衰力の減少をもたらすことにな
る。これらのために、緩衝器用油圧作動油に対して、低
温粘度特性と蒸発性、及び剪断安定性に優れ、高温から
低温に渡って減衰力安定性が良好な緩衝器用油圧作動油
の開発が強く望まれている。
[0005] Since the shock absorber is used in a relatively wide temperature range, it is necessary to reduce a change in viscosity due to temperature and to prevent a change in damping force. In particular, the viscosity of the hydraulic fluid for a shock absorber increases at low temperatures, and when the viscosity at low temperatures becomes too high, the damping force becomes large and smooth operation cannot be performed, and ride comfort and steering stability deteriorate. Therefore, recently, the requirement for maintaining the damping force at a low temperature has become strict, and for example, it is required to greatly reduce the damping force at a low temperature of -20 ° C to -40 ° C. Therefore, there is a strong demand for a hydraulic oil for a shock absorber having good low-temperature viscosity characteristics. However, conventional hydraulic fluids for shock absorbers contain a viscosity index improver or a pour point depressant in a low-viscosity base oil. And there is a disadvantage that the amount of evaporation increases and the damping force fluctuates due to cavitation. Furthermore, hydraulic fluids for shock absorbers containing a large amount of viscosity index improvers and pour point depressants are
The oil is sheared when the piston slides or the oil flows in the orifice, and the viscosity of the hydraulic oil for the shock absorber decreases.
A significant decrease in viscosity will result in a decrease in damping force. For these reasons, the development of hydraulic fluids for shock absorbers, which have excellent low-temperature viscosity characteristics, evaporative properties, and shear stability, and good damping force stability from high to low temperatures, has been strongly developed. Is desired.

【0006】[0006]

【発明が解決しようとする課題】上記のような開発状況
に鑑み、本発明の目的は、低温粘度特性、蒸発性、及び
剪断安定性に優れ、高温から低温に渡って減衰力安定性
が良好な緩衝器用油圧作動油組成物を提供することにあ
る。
SUMMARY OF THE INVENTION In view of the above situation, an object of the present invention is to provide excellent low-temperature viscosity characteristics, excellent evaporability and shear stability, and good damping force stability from high to low temperatures. Another object of the present invention is to provide a hydraulic oil composition for a shock absorber.

【0007】[0007]

【課題を解決するための手段】本発明者らは、前記した
従来技術の問題点を解消するために鋭意研究を重ねた結
果、特定性状の深脱蝋鉱油、及び/又は特定性状の合成
油の潤滑油基油に、ポリメタクリレート系、オレフィン
コポリマー系、星状ポリマーなどの粘度指数向上剤及び
/又はアクリレート系、ポリメタクリレート系などの流
動点降下剤を特定量配合し、しかも緩衝器用油圧作動油
の100℃における動粘度、粘度指数、かつ−40℃に
おけるブルックフィールド粘度を特定範囲内にすること
により、緩衝器用油圧作動油として要求される低温粘度
特性、蒸発性、及び剪断安定性に優れ、高温から低温に
渡って減衰力安定性が良好な緩衝器用油圧作動油組成物
が得られることを見い出した。本発明は、これらの知見
に基づいて完成するに至ったものである。すなわち、本
発明によれば、下記の鉱油(A)及び/又は合成油
(B)からなる基油に、組成物全量を基準として20重
量%以下の粘度指数向上剤及び/又は流動点降下剤を配
合してなる緩衝器用油圧作動油組成物であって、その粘
度特性は、100℃における動粘度が1〜20mm
s、粘度指数が140以上であり、かつ、−40℃にお
けるブルックフィールド粘度が2000mPa・s以下
であることを特徴とする緩衝器用油圧作動油組成物が提
供される。 鉱油(A):100℃における動粘度が2〜3mm
s、流動点が−30℃以下、及び曇り点が−27.5℃
以下である深脱蝋鉱油(a)、又は該深脱蝋鉱油(a)
と、40℃における動粘度が1.0〜6.0mm/s
である低粘度鉱油(b)との混合鉱油(ただし、該低粘
度鉱油(b)の含有量は、混合鉱油全量を基準として2
0重量%未満である)。 合成油(B):100℃における動粘度が1.5〜45
mm/sであるポリα−オレフィン(c)、及び/又
は100℃における動粘度が1.5〜20mm /s及
び流動点が−30℃以下であるエステル化合物(d)。
Means for Solving the Problems The present inventors have described the above-mentioned.
After intensive research to solve the problems of the prior art
Fruit, deep-dewaxed mineral oil of specific properties, and / or synthesis of specific properties
Oil lubricating base oil, polymethacrylate, olefin
Viscosity index improvers such as copolymers and star polymers;
/ Or acrylate, polymethacrylate, etc.
Hydraulic fluid for shock absorbers with specific amount of moving point depressant
Kinematic viscosity at 100 ° C, viscosity index, and -40 ° C
The Brookfield viscosity in the specified range
Low temperature viscosity required as hydraulic fluid for shock absorber
Excellent properties, evaporability and shear stability, from high to low temperatures
Hydraulic fluid composition for shock absorber with good damping force stability over the whole
Was obtained. The present invention is based on these findings.
It was completed based on. That is, the book
According to the invention, the following mineral oil (A) and / or synthetic oil
20 bases on the base oil consisting of (B) based on the total amount of the composition
% Or less of a viscosity index improver and / or a pour point depressant.
A hydraulic oil composition for a shock absorber, comprising:
The kinematic viscosity at 100 ° C. is 1 to 20 mm2/
s, viscosity index is 140 or more and at -40 ° C
Brookfield viscosity of 2000 mPa · s or less
A hydraulic fluid composition for a shock absorber characterized by
Provided. Mineral oil (A): kinematic viscosity at 100 ° C. is 2 to 3 mm2/
s, pour point of -30 ° C or less, and cloud point of -27.5 ° C
Or a deeply dewaxed mineral oil (a), or
And the kinematic viscosity at 40 ° C. is 1.0 to 6.0 mm2/ S
Mineral oil mixed with a low-viscosity mineral oil (b)
The mineral oil (b) content is 2% based on the total amount of the mixed mineral oil.
Less than 0% by weight). Synthetic oil (B): kinematic viscosity at 100 ° C. is 1.5 to 45.
mm2/ S of poly-α-olefin (c), and / or
Is a kinematic viscosity at 100 ° C. of 1.5 to 20 mm 2/ S and
And an ester compound (d) having a pour point of -30 ° C or lower.

【0008】本発明は、上記した如く、低温粘度特性、
蒸発性、及び剪断安定性に優れ、高温から低温に渡って
減衰力安定性が良好な緩衝器用油圧作動油組成物に係わ
るものであるが、その好ましい態様としては、次のもの
が包含される。 (イ)基油が、100℃における動粘度が2〜3mm
/s、流動点が−30℃以下、及び曇り点が−27.5
℃以下の深脱蝋鉱油(a)である上記記載の緩衝器用油
圧作動油組成物。 (ロ)基油が、100℃における動粘度が2〜3mm
/s、流動点が−30℃以下、及び曇り点が−27.5
℃以下である深脱蝋鉱油(a)と、40℃における動粘
度が1.0〜6.0mm/sである低粘度鉱油(b)
との混合鉱油(ただし、該低粘度鉱油(b)の含有量
は、混合鉱油全量を基準として20重量%未満である)
である上記記載の緩衝器用油圧作動油組成物。 (ハ)基油が、100℃における動粘度が2〜3mm
/s、流動点が−30℃以下、及び曇り点が−27.5
℃以下である深脱蝋鉱油(a)と、40℃における動粘
度が1.0〜2.5mm/sである低粘度鉱油
(b)との混合鉱油(ただし、該低粘度鉱油(b
の含有量は、混合鉱油全量を基準として20重量%未満
である)である上記記載の緩衝器用油圧作動油組成物。 (ニ)基油が、100℃における動粘度が2〜3mm
/s、流動点が−30℃以下、及び曇り点が−27.5
℃以下である深脱蝋鉱油(a)と、40℃における動粘
度が2.5〜6.0mm/sである低粘度鉱油
(b)との混合鉱油(ただし、該低粘度鉱油(b
の含有量は、混合鉱油全量を基準として20重量%未満
である)である上記記載の緩衝器用油圧作動油組成物。 (ホ)100℃における動粘度が2〜3mm/s、流
動点が−35℃以下、及び曇り点が−30℃以下の深脱
蝋鉱油である前記(イ)〜(ニ)のいずれかに記載の緩
衝器用油圧作動油組成物。 (ヘ)基油が、100℃における動粘度が1.5〜45
mm/sであるポリα−オレフィン(c)、及び/又
は100℃における動粘度が1.5〜20mm/s及
び流動点が−30℃以下であるエステル化合物(d)か
らなる合成油である上記記載の緩衝器用油圧作動油組成
物。 (ト)ポリα−オレフィン(c)とエステル化合物
(d)との混合割合が、(c)70〜90重量%、
(d)10〜30重量%である前記(ヘ)記載の緩衝器
用油圧作動油組成物。 (チ)基油が、100℃における動粘度が2〜3mm
/s、流動点が−30℃以下、及び曇り点が−27.5
℃以下である深脱蝋鉱油(a)と、100℃における動
粘度が1.5〜45mm/sであるポリα−オレフィ
ン(c)及び/又は100℃における動粘度が1.5〜
20mm/s及び流動点が−30℃以下であるエステ
ル化合物(d)との部分合成油である上記記載の緩衝器
用油圧作動油組成物。 (リ)基油が、100℃における動粘度が2〜3mm
/s、流動点が−30℃以下、及び曇り点が−27.5
℃以下である深脱蝋鉱油(a)及び40℃における動粘
度が1.0〜6.0mm/sである低粘度鉱油(b)
との混合鉱油(ただし、該低粘度鉱油(b)の含有量
は、混合鉱油全量を基準として20重量%未満である)
と、100℃における動粘度が1.5〜45mm/s
であるポリα−オレフィン(c)及び/又は100℃に
おける動粘度が1.5〜20mm/s及び流動点が−
30℃以下であるエステル化合物(d)との部分合成油
である上記記載の緩衝器用油圧作動油組成物。 (ヌ)ポリメタクリレート系、オレフィンコポリマー
系、星状ポリマー等、一般的な潤滑油用粘度指数向上剤
及び/又はアクリレート系、ポリメタクリレート系など
の流動点降下剤(e)を20重量%以下に配合した上記
記載の緩衝器用油圧作動油組成物。
[0008] As described above, the present invention provides a low-temperature viscosity property,
The present invention relates to a hydraulic fluid composition for a shock absorber having excellent evaporability and shear stability and good damping force stability from high to low temperatures. Preferred embodiments thereof include the following. . (A) the base oil has a kinematic viscosity at 100 ° C. of 2 to 3 mm 2;
/ S, a pour point of −30 ° C. or less, and a cloud point of −27.5.
The hydraulic oil composition for a shock absorber according to the above, which is a deep dewaxed mineral oil (a) having a temperature of not more than 0 ° C. (B) the base oil has a kinematic viscosity at 100 ° C. of 2 to 3 mm 2;
/ S, a pour point of −30 ° C. or less, and a cloud point of −27.5.
Deep-wax mineral oil (a) at a temperature of 40 ° C. or lower and low-viscosity mineral oil (b) having a kinematic viscosity at 40 ° C. of 1.0 to 6.0 mm 2 / s.
(However, the content of the low-viscosity mineral oil (b) is less than 20% by weight based on the total amount of the mixed mineral oil)
The hydraulic oil composition for a shock absorber according to the above. (C) the base oil has a kinematic viscosity at 100 ° C of 2 to 3 mm 2;
/ S, a pour point of −30 ° C. or less, and a cloud point of −27.5.
And a low viscosity mineral oil (b 1 ) having a kinematic viscosity of 1.0 to 2.5 mm 2 / s at 40 ° C. (wherein the low viscosity mineral oil (a) b 1 )
Is less than 20% by weight based on the total amount of the mixed mineral oil). (D) the base oil has a kinematic viscosity at 100 ° C. of 2 to 3 mm 2;
/ S, a pour point of −30 ° C. or less, and a cloud point of −27.5.
And a low viscosity mineral oil (b 2 ) having a kinematic viscosity at 40 ° C. of 2.5 to 6.0 mm 2 / s (provided that the low viscosity mineral oil (a) b 2 )
Is less than 20% by weight based on the total amount of the mixed mineral oil). (E) any of the above (a) to (d), which is a deep dewaxed mineral oil having a kinematic viscosity at 100 ° C of 2 to 3 mm 2 / s, a pour point of -35 ° C or less, and a cloud point of -30 ° C or less. 3. The hydraulic oil composition for a shock absorber according to the item 1. (F) the base oil has a kinematic viscosity at 100 ° C of 1.5 to 45;
mm 2 / s at which poly α- olefin (c), and / or 100 the kinematic viscosity at ° C. consists 1.5~20mm 2 / s and an ester compound are pour point of -30 ° C. or less (d) synthetic oils The hydraulic oil composition for a shock absorber according to the above. (G) the mixing ratio of the poly α-olefin (c) and the ester compound (d) is (c) 70 to 90% by weight,
(D) The hydraulic oil composition for a shock absorber according to the above (f), which is 10 to 30% by weight. (H) the base oil has a kinematic viscosity at 100 ° C of 2 to 3 mm 2;
/ S, a pour point of −30 ° C. or less, and a cloud point of −27.5.
Deep-wax mineral oil (a) having a kinematic viscosity at 100 ° C. of 1.5 to 45 mm 2 / s and / or a kinematic viscosity at 100 ° C. of 1.5 to 45 mm 2 / s.
The hydraulic oil composition for a shock absorber as described above, which is a partially synthetic oil with an ester compound (d) having a flow point of 20 mm 2 / s and a pour point of −30 ° C. or lower. (I) the base oil has a kinematic viscosity at 100 ° C of 2 to 3 mm 2;
/ S, a pour point of −30 ° C. or less, and a cloud point of −27.5.
Deep dewaxed mineral oil (a) having a kinematic viscosity of 1.0 to 6.0 mm 2 / s at 40 ° C. or lower (b).
(However, the content of the low-viscosity mineral oil (b) is less than 20% by weight based on the total amount of the mixed mineral oil)
And the kinematic viscosity at 100 ° C. is 1.5 to 45 mm 2 / s
And the kinematic viscosity at 100 ° C. is 1.5 to 20 mm 2 / s and the pour point is −
The hydraulic oil composition for a shock absorber according to the above, which is a partially synthetic oil with the ester compound (d) having a temperature of 30 ° C. or lower. (N) To reduce the viscosity index improver for general lubricating oils such as polymethacrylates, olefin copolymers and star polymers and / or pour point depressants (e) such as acrylates and polymethacrylates to 20% by weight or less. The blended hydraulic oil composition for a shock absorber as described above.

【0009】[0009]

【発明の実施の形態】以下、本発明を詳細に説明する。 (1)潤滑油基油 本発明の緩衝器用油圧作動油組成物において、基油とし
て用いる深脱蝋鉱油(a)は、パラフィン系原油又は中
間基原油を蒸留して得られた留出油を常法に従って精製
した後、深脱蝋処理を行なうことによって得ることがで
きる。なお、留出油とは原油を常圧蒸留するかあるいは
常圧蒸留の残渣油を減圧蒸留して得られるものを意味す
る。精製法は特に制限はないが、次の〜のいずれか
の処理をすることによって得ることができる。 留出油を水素化処理するか、又は水素化処理したの
ち、アルカリ蒸留若しくは硫酸洗浄を行なう。 留出油を溶剤精製処理するか、又は溶剤精製処理した
後、アルカリ蒸留若しくは硫酸洗浄を行なう。 留出油を水素化処理したのち、続いて第2段目の水素
化処理を行なう。 留出油を水素化処理したのち、第2段目の水素化処
理、さらに第3段目の水素化処理を行なう。 留出油を水素化処理したのち、第2段目の水素化処理
を行ない、さらにアルカリ蒸留若しくは硫酸洗浄を行な
う。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. (1) Lubricating oil base oil In the hydraulic oil composition for a shock absorber of the present invention, the deeply dewaxed mineral oil (a) used as the base oil is a distillate obtained by distilling a paraffinic crude oil or an intermediate base crude oil. It can be obtained by performing a deep dewaxing treatment after purifying according to a conventional method. The distillate refers to one obtained by distilling crude oil at normal pressure or distilling residual oil of normal pressure under reduced pressure. The purification method is not particularly limited, but can be obtained by any one of the following treatments. The distillate is subjected to a hydrotreating process or a hydrotreating process, followed by alkali distillation or sulfuric acid washing. The distillate is subjected to a solvent refining treatment or a solvent refining treatment, followed by alkali distillation or sulfuric acid washing. After hydrotreating the distillate, a second-stage hydrotreatment is performed. After hydrotreating the distillate, a second-stage hydrotreatment and a third-stage hydrotreatment are performed. After hydrotreating the distillate, a second-stage hydrotreatment is performed, followed by alkali distillation or sulfuric acid washing.

【0010】以下に処理法の1例を示す。パラフィン系
原油又は中間基原油から常法により、潤滑油粗原料を調
製し、苛酷な水素化処理を行なう。この処理によって芳
香族分などの潤滑油留分に好ましくない成分を除去した
り、有効な成分に変えたりする反応が行なわれる。この
際、硫黄分や窒素分も殆んど除去される。次いで、減圧
蒸留により必要な粘度を得るような分留を行なう。しか
る後に、既知の溶剤脱蝋を行ない、通常のパラフィン系
基油が有する流動点、すなわち−15〜−10℃程度に
脱蝋する。この脱蝋処理後、必要に応じてさらに水素化
処理を行ない芳香族分の大部分を水素化させて飽和分と
し、基油の熱的、化学的な安定性を向上させる。しか
し、流動点が未だ高いため潤滑油としては適当でない。
そのために引続き深脱蝋処理が行なわれる。この深脱蝋
処理は、苛酷な条件での溶剤脱蝋法や、ゼオライト触媒
を用い、該触媒の細孔に吸着されるパラフィン(主とし
てノルマルパラフィン)を選択的に水素雰囲気下で分解
して蝋分となるものを除去する接触水添脱蝋法が適用さ
れる。水素化処理は原料油の性状等により異なるが、通
常は反応温度200〜480℃、好ましくは250〜4
80℃,水素圧力5〜300kg/cm、好ましくは
30〜250kg/cm、水素導入量(対供給留出油
1kl当り)30〜3000Nm、好ましくは100
〜2000Nmの条件で行なわれる。また、この際に
用いられる触媒は担体としてアルミナ,シリカ,シリカ
・アルミナ,ゼオライト,活性炭,ボーキサイトなどを
用い、周期律表第VI族、第VIII族などの金属、好
ましくはコバルト,ニッケル,モリブデン,タングステ
ンなどの触媒成分を既知の方法で担持させたものが使用
される。なお、触媒は予め予備硫化したものが好まし
い。上記した如く、留出油は水素化処理した後、種々の
処理が行なわれるが、第2段目あるいは第3段目の水素
化処理を行なう場合、水素化処理条件は上記範囲内で設
定すればよく、第1〜3段目の各条件は同一であっても
よく異なってもよい。しかし、通常は第1段目よりは第
2段目、第2段目よりは第3段目の条件を厳しくして行
なわれる。次に、アルカリ蒸留は、微量の酸性物質を除
去して留出分の安定性を改良する工程として行なわれ、
NaOH,KOH等のアルカリを加えて減圧蒸留するこ
とにより行なう。また、硫酸洗浄は、一般に石油製品の
仕上げ工程として行なわれているものであり、芳香族炭
化水素、特に多環芳香族炭化水素やオレフィン類,硫黄
化合物などを除去して留出油の性状を改善するために適
用される。なお、留出油の処理は上記操作の組合せによ
り前記した如く〜の具体的方法があるが、これら方
法の中では特に,,の方法が好適である。
An example of the processing method will be described below. A crude lubricating oil raw material is prepared from a paraffinic crude oil or an intermediate base crude oil by an ordinary method and subjected to severe hydrotreating. By this treatment, a reaction is performed to remove components that are not desirable in the lubricating oil fraction such as aromatic components or to convert them into effective components. At this time, most of sulfur and nitrogen are also removed. Next, fractional distillation is performed to obtain the required viscosity by distillation under reduced pressure. Thereafter, known solvent dewaxing is performed to dewax to the pour point of ordinary paraffinic base oil, that is, about -15 to -10 ° C. After this dewaxing treatment, if necessary, further hydrogenation treatment is carried out to hydrogenate most of the aromatics to a saturated content, thereby improving the thermal and chemical stability of the base oil. However, since the pour point is still high, it is not suitable as a lubricating oil.
For this purpose, a deep dewaxing process is subsequently performed. This deep dewaxing treatment is carried out under a severe solvent dewaxing method, or by using a zeolite catalyst to selectively decompose paraffin (mainly normal paraffin) adsorbed in the pores of the catalyst under a hydrogen atmosphere to obtain a wax. A catalytic hydrogenation dewaxing method is applied to remove the components. The hydrotreating varies depending on the properties of the feedstock oil, etc., but usually the reaction temperature is from 200 to 480 ° C., preferably from 250 to 4 ° C.
80 ° C., hydrogen pressure 5 to 300 kg / cm 2 , preferably 30 to 250 kg / cm 2 , hydrogen introduction amount (per 1 kl of feed distillate) 30 to 3000 Nm 3 , preferably 100
It is performed under the condition of 20002000 Nm 3 . The catalyst used at this time uses alumina, silica, silica-alumina, zeolite, activated carbon, bauxite or the like as a carrier, and a metal such as Group VI or VIII of the periodic table, preferably cobalt, nickel, molybdenum, or the like. A catalyst component such as tungsten supported by a known method is used. Preferably, the catalyst is preliminarily sulfurized. As described above, the distillate is subjected to various treatments after the hydrotreating. When the second or third stage hydrotreating is performed, the hydrotreating conditions are set within the above range. The conditions in the first to third stages may be the same or different. However, usually, the conditions are set stricter in the second stage than in the first stage and in the third stage than in the second stage. Next, alkali distillation is performed as a step of improving the stability of the distillate by removing a trace amount of acidic substances,
This is performed by adding an alkali such as NaOH or KOH and performing distillation under reduced pressure. Sulfuric acid washing is generally performed as a finishing step for petroleum products, and removes aromatic hydrocarbons, particularly polycyclic aromatic hydrocarbons, olefins, sulfur compounds, and the like, to improve the properties of distillate oil. Applied to improve. In addition, there are the above-mentioned specific methods for the treatment of the distillate according to a combination of the above-mentioned operations, and among these methods, the method is particularly preferable.

【0011】本発明に用いられる深脱蝋基油(a)は、
上記の方法によって得ることができるが、100℃にお
ける動粘度が2〜3mm/s、好ましくは2〜2.5
mm /s、流動点が−30℃以下、好ましくは−35
℃以下、曇り点が−27.5℃以下、好ましくは−3
0.0℃以下である必要がある。100℃における動粘
度が2mm/s未満であると、耐摩耗性が低下し、蒸
発特性が悪化するので好ましくない。一方、3mm
sを超えると低温での粘度特性、すなわち低温流動性が
低下するので好ましくない。また、流動点が−30℃及
び曇り点が−27.5℃を超えると低温流動性が低下す
るので好ましくない。
The deeply dewaxed base oil (a) used in the present invention is:
It can be obtained by the above method,
Kinematic viscosity is 2-3mm2/ S, preferably 2 to 2.5
mm 2/ S, pour point of -30 ° C or less, preferably -35
° C or less, and the cloud point is -27.5 ° C or less, preferably -3.
It needs to be 0.0 ° C. or less. Kinematic viscosity at 100 ° C
Degree is 2mm2/ S, the abrasion resistance is reduced,
This is not preferable because the emission characteristics deteriorate. On the other hand, 3mm2/
If the viscosity exceeds s, viscosity characteristics at low temperature, that is, low-temperature fluidity,
It is not preferable because it lowers. In addition, the pour point is -30 ° C.
If the cloud point exceeds -27.5 ° C, the low-temperature fluidity decreases.
This is not preferred.

【0012】また、本発明の緩衝器用油圧作動油組成物
において、上記の深脱蝋鉱油に、混合して用いることが
できる低粘度基油として、40℃における動粘度が1.
0〜6.0mm/sである低粘度鉱油(b)があり、
例えば、40℃における動粘度が1.0〜2.5mm
/sの鉱油(b)、好ましくは40℃における動粘度
が1.5〜2.1mm/sの鉱油、又は40℃におけ
る動粘度が2.5〜6.0mm/sの鉱油(b)、
好ましくは40℃における動粘度が2.6〜3.5mm
/sの鉱油などが挙げられる。上記の深脱蝋鉱油に、
これらの低粘度鉱油を混合することにより、深脱蝋鉱油
単独の場合よりも飛躍的に低温流動性を高めることがで
きる。40℃における動粘度が1mm/s未満である
と、耐摩耗性が低下し、蒸発特性が悪化するので好まし
くない。一方、6mm/sを超えると低温での粘度特
性、すなわち低温流動性が低下するので好ましくない。
本発明おいて、緩衝器用油圧作動油組成物の基油とし
て、上記した深脱蝋鉱油(a)と低粘度鉱油(b)との
混合鉱油を用いた場合、該低粘度鉱油(b)の含有量
は、混合鉱油全量を基準として20重量%未満である必
要がある。好ましくは、10重量%以下である。ここで
混合割合が上記範囲外であると、蒸発特性が劣ったもの
となり、しかも緩衝器用油圧作動油本来の潤滑特性や摩
擦特性も不充分となるため好ましくない。
In the hydraulic fluid composition for a shock absorber according to the present invention, a low-viscosity base oil having a kinematic viscosity at 40.degree.
There is a low-viscosity mineral oil (b) that is 0-6.0 mm 2 / s,
For example, the kinematic viscosity at 40 ° C. is 1.0 to 2.5 mm 2
/ S mineral oil (b 1 ), preferably a mineral oil having a kinematic viscosity at 40 ° C. of 1.5 to 2.1 mm 2 / s, or a mineral oil having a kinematic viscosity at 40 ° C. of 2.5 to 6.0 mm 2 / s ( b 2 ),
Preferably, the kinematic viscosity at 40 ° C. is 2.6 to 3.5 mm.
2 / s mineral oil and the like. In the above deep dewaxed mineral oil,
By mixing these low-viscosity mineral oils, the low-temperature fluidity can be drastically improved as compared with the case of using deeply dewaxed mineral oil alone. If the kinematic viscosity at 40 ° C. is less than 1 mm 2 / s, the abrasion resistance decreases and the evaporation characteristics deteriorate, which is not preferable. On the other hand, if it exceeds 6 mm 2 / s, the viscosity characteristics at low temperature, that is, the low-temperature fluidity decreases, which is not preferable.
In the present invention, when a mixed mineral oil of the deeply dewaxed mineral oil (a) and the low-viscosity mineral oil (b) is used as a base oil of the hydraulic oil composition for a shock absorber, the low-viscosity mineral oil (b) The content should be less than 20% by weight based on the total amount of the mixed mineral oil. Preferably, it is at most 10% by weight. If the mixing ratio is outside the above range, the evaporation characteristics are inferior, and the lubricating characteristics and friction characteristics inherent to the hydraulic oil for shock absorbers are also unsatisfactory.

【0013】本発明の緩衝器用油圧作動油組成物におい
て、基油として用いるポリα−オレフィン(c)は、α
−オレフィンオリゴマーとも称される合成潤滑油であっ
て、次の一般式〔I〕
In the hydraulic fluid composition for a shock absorber according to the present invention, the poly α-olefin (c) used as the base oil is α
A synthetic lubricating oil, also called an olefin oligomer, having the following general formula [I]

【0014】[0014]

【化1】 Embedded image

【0015】(式中、Rは炭素数4〜12のアルキル基
を示し、mは0〜30を示す。)で表わされるものであ
る。ここでポリα−オレフィンとしては100℃におけ
る動粘度が1.5〜45mm/s、好ましくは1.7
〜40mm/sのものが用いられる。ここで、動粘度
が1.5mm/s未満のものは、蒸発量が多いという
不都合があり、一方45mm/sを超えるものでは、
低温粘度特性が悪くなるので好ましくない。具体的には
1−オクテン,1−デセン,1−ドデセンの2〜10量
体,好ましくは1−デセンの2〜4量体の如き低重合度
のポリα−オレフィンを用いることが粘度指数、流動点
の点から望ましい。このようなポリα−オレフィンは、
重合工程,触媒分解工程,蒸留工程,水素化工程からな
る公知の方法により製造することができる。また、重合
度の調節は重合工程における反応器の滞留時間を変更す
ることなどにより行なえばよい。
(Wherein, R represents an alkyl group having 4 to 12 carbon atoms, and m represents 0 to 30). Here, the poly-α-olefin has a kinematic viscosity at 100 ° C. of 1.5 to 45 mm 2 / s, preferably 1.7.
の も の 40 mm 2 / s is used. Here, when the kinematic viscosity is less than 1.5 mm 2 / s, there is a disadvantage that the evaporation amount is large. On the other hand, when the kinematic viscosity exceeds 45 mm 2 / s,
It is not preferable because the low-temperature viscosity characteristics deteriorate. Specifically, it is preferable to use a poly-α-olefin having a low polymerization degree such as a 2- to 10-mer of 1-octene, 1-decene, or 1-dodecene, preferably a 2- to 4-mer of 1-decene. Desirable in terms of pour point. Such a poly-α-olefin is
It can be produced by a known method comprising a polymerization step, a catalytic decomposition step, a distillation step, and a hydrogenation step. The degree of polymerization may be adjusted by changing the residence time of the reactor in the polymerization step.

【0016】本発明の緩衝器用油圧作動油組成物におい
て、基油として用いるエステル化合物(d)は、100
℃における動粘度が1.5〜20mm/s、流動点が
−30℃以下であるエステル化合物であれば用いること
ができるが、好ましいのは、100℃における動粘度が
1.5〜10mm/s、流動点が−35℃以下のもの
である。このようなエステル化合物としては、例えば、
二塩基酸エステル(ジエステル)やポリオールエステル
(ヒンダードエステル)などが挙げられ、特に二塩基酸
エステル(ジエステル)が、高粘度指数や低温流動性等
の観点から好適である。二塩基酸エステルは、普通、二
塩基酸1に対しアルコール2の割合でエステル化反応さ
せたものである。二塩基酸エステルの原料である二塩基
酸としては、アジピン酸、アゼライン酸、セバシン酸、
ドデカン二酸などが用いられ、アルコールとしては、炭
素数7〜13で側鎖をもった第一級アルコールがよく用
いられ、例えば、Cの2−エチルヘキサノール、C
12のイソデカノール、C13のトリデカノールなどが
挙げられる。二塩基酸エステルとしては、例えば、ジ−
2−エチルヘキシルセバケート(DOS)、ジ−2−エ
チルヘキシルシアジペート(DOA)、ジイソデシルア
ジペート(DIDA)、ジイソオクチルアジペート(D
IOA)、ジ−2−エチルヘキシルアゼレート(DO
Z)などが挙げられる。ポリオールエステルは、普通、
ネオペンチルポリオールと一塩基性脂肪酸のエステルで
ある。ポリオールエステルの原料であるネオペンチルポ
リオールとしては、二価のアルコールとしてネオペンチ
ルグリコール(NPG)、三価のものとしてトリメチロ
ールプロパン(TMP)やトリメチロールエタン(TM
E)、四価のものとしてペンタエリスリトール(P
E)、六価のものとしてジペンタエリスリトール(DP
E)があり、トリメチロールプロパン(TMP)とペン
タエリスリトール(PE)がよく用いられる。原料の一
塩基性脂肪酸としては、直鎖や分枝型のC〜C13
ものがよく用いられ、流動点を改良するために、炭素数
の異なる何種類かの直鎖の酸の混合物や分枝酸を少量混
ぜて用いることが多い。
In the hydraulic fluid composition for a shock absorber according to the present invention, the ester compound (d) used as the base oil is 100%.
An ester compound having a kinematic viscosity at 1.5 ° C. of 1.5 to 20 mm 2 / s and a pour point of −30 ° C. or less can be used, but a kinematic viscosity at 100 ° C. of 1.5 to 10 mm 2 is preferable. / S and a pour point of -35 ° C or less. Such ester compounds include, for example,
Examples thereof include dibasic acid esters (diesters) and polyol esters (hindered esters), and dibasic acid esters (diesters) are particularly preferable from the viewpoints of high viscosity index, low-temperature fluidity, and the like. The dibasic acid ester is usually one obtained by subjecting one dibasic acid to an esterification reaction at a ratio of two alcohols. Dibasic acids which are the raw materials for dibasic acid esters include adipic acid, azelaic acid, sebacic acid,
Such as dodecanedioic acid is used as the alcohol, a primary alcohol is often used having a side chain with 7 to 13 carbon atoms, for example, the C 2 2-ethylhexanol, C
12 of isodecanol and tridecanol of C 13 and the like. As the dibasic acid ester, for example, di-
2-ethylhexyl sebacate (DOS), di-2-ethylhexyl siadipate (DOA), diisodecyl adipate (DIDA), diisooctyl adipate (D
IOA), di-2-ethylhexyl azelate (DO
Z) and the like. Polyol esters are usually
It is an ester of neopentyl polyol and a monobasic fatty acid. Neopentyl polyol, which is a raw material of polyol ester, includes neopentyl glycol (NPG) as a dihydric alcohol, and trimethylolpropane (TMP) or trimethylolethane (TM) as a trivalent alcohol.
E), pentaerythritol (P
E), dipentaerythritol (DP
E), and trimethylolpropane (TMP) and pentaerythritol (PE) are often used. As the raw material monobasic fatty acid, a linear or branched C 3 -C 13 fatty acid is often used. In order to improve the pour point, a mixture of several types of linear acids having different carbon numbers is used. Or a small amount of a branched acid.

【0017】本発明では、緩衝器用油圧作動油組成物の
基油として、前記のポリα−オレフィン及び/又はエス
テル化合物を使用することができる。これらは、それぞ
れ単独で、あるいは両者を組み合わせて使用することが
できるが、ポリα−オレフィンとエステル化合物を組み
合わせて使用することが好ましい。ポリα−オレフィン
(c)とエステル化合物(d)との配合割合(c:d)
は、重量比で、通常、50:50〜95:5、好ましく
は70:30〜90:10、より好ましくは75:25
〜85:15である。この配合割合の範囲内にあること
によって、シールゴムとの適合性に優れ、かつ粘度指数
が高く、低温粘度特性を優れたものにすることができ
る。また、本発明では、緩衝器用油圧作動油組成物の基
油として、前記の鉱油(A)と合成油(B)をそれぞれ
単独で又は両者を組み合わせて用いてもよい。
In the present invention, the above-mentioned poly-α-olefin and / or ester compound can be used as the base oil of the hydraulic oil composition for a shock absorber. These can be used alone or in combination of both, but it is preferable to use a combination of a poly-α-olefin and an ester compound. Compounding ratio of poly α-olefin (c) and ester compound (d) (c: d)
Is usually 50:50 to 95: 5, preferably 70:30 to 90:10, and more preferably 75:25 by weight.
85:15. By being in this range, the compatibility with the seal rubber is excellent, the viscosity index is high, and the low-temperature viscosity characteristics can be improved. In the present invention, the mineral oil (A) and the synthetic oil (B) may be used alone or in combination as the base oil of the hydraulic oil composition for a shock absorber.

【0018】(2)粘度指数向上剤及び/又は流動点降
下剤(e) 本発明の緩衝器用油圧作動油組成物に配合される粘度指
数向上剤及び/又は流動点降下剤(e)は、粘度指数向
上剤と流動点降下剤、それぞれ単独又は両者を組み合わ
せて用いられる。粘度指数向上剤としては、ポリメタク
リレート系、オレフィンコポリマー系、星状ポリマー
等、一般的な潤滑油用粘度指数向上剤を用いることがで
き、流動点降下剤としては、アクリレート系、ポリメタ
クリレート系などを用いることができる。粘度指数向上
剤は、好ましくは、ポリメタクリレート系が用いられ、
ポリメタクリレート系の粘度指数向上剤は、分散型と非
分散型があり、いずれを用いてもよい。重量平均分子量
は、10,000〜300,000のものが好ましく用
いられ、特に好ましいのは10,000〜120,00
0のものである。重量平均分子量が10,000未満の
ものは、剪断安定性はよいものの低温粘度低減効果は小
さく、一方、300,000を超えるものは、低温粘度
低減効果は大きいものの剪断安定性は悪い。粘度指数向
上剤及び/又は流動点降下剤(e)の配合量は、組成物
全量に対して20重量%以下である。好ましくは、4〜
10重量%である。配合量が20重量%を超えると剪断
安定性が悪化するとともに、低温粘度が大きくなってし
まう。
(2) Viscosity index improver and / or pour point depressant (e) The viscosity index improver and / or pour point depressant (e) incorporated in the hydraulic fluid composition for a shock absorber of the present invention are: The viscosity index improver and the pour point depressant are used alone or in combination. As the viscosity index improver, general viscosity index improvers for lubricating oils such as polymethacrylates, olefin copolymers, and star polymers can be used. As pour point depressants, acrylates, polymethacrylates, and the like can be used. Can be used. The viscosity index improver is preferably a polymethacrylate type,
Polymethacrylate-based viscosity index improvers include a dispersion type and a non-dispersion type, and any of them may be used. Those having a weight average molecular weight of 10,000 to 300,000 are preferably used, and particularly preferably 10,000 to 120,000.
0. When the weight average molecular weight is less than 10,000, the shear stability is good but the low-temperature viscosity reduction effect is small. On the other hand, when the weight average molecular weight exceeds 300,000, the low temperature viscosity reduction effect is large but the shear stability is poor. The compounding amount of the viscosity index improver and / or the pour point depressant (e) is 20% by weight or less based on the total amount of the composition. Preferably, 4-
10% by weight. If the amount is more than 20% by weight, the shear stability is deteriorated and the low-temperature viscosity is increased.

【0019】(3)その他の添加剤 本発明の緩衝器用油圧作動油組成物には、本発明の目的
を損なわない限り、必要に応じてその他の添加剤、例え
ば、摩擦調整剤、耐摩耗剤、酸化防止剤、無灰清浄分散
剤、金属清浄剤、腐食防止剤、防錆剤、消泡剤などを適
宜添加することができる。摩擦調整剤としては、脂肪酸
(オレイン酸、ステアリン酸など)、高級アルコール
(オレイルアルコールなど)、脂肪酸エステル、リン酸
エステル、亜りん酸エステル、りん酸エステルアミン
塩、油脂類、多価アルコールエステル、ソルビタンエス
テル、脂肪族アミン等を挙げることができ、これらは、
通常、0.05〜3.0重量%の割合で使用される。耐
摩耗剤としては、ジチオりん酸金属塩(Zn、Pb、S
b、Moなど)、ジチオカルバミン酸金属塩(Zn、M
oなど)ナフテン酸金属塩(Pbなど)、脂肪酸金属塩
(Pbなど)、リン酸エステル、亜りん酸エステル、り
ん酸エステルアミン塩、硫化油脂、硫黄化合物、ホウ素
化合物、等を挙げることができ、これらは、通常、0.
05〜3.0重量%の割合で使用される。酸化防止剤と
しては、アルキル化ジフェニルアミン、フェニル−α−
ナフチルアミン、アルキル化フェニル−α−ナフチルア
ミン等のアミン系酸化防止剤、2,6−ジ−t−ブチル
フェノール、4,4’−メチレンビス−(2,6−ジタ
ーシャリブチルフェノール)等のフェノール系酸化防止
剤、ホスファイト等のりん系酸化防止剤、ジラウリル−
3,3’−チオジプロピオネイト等の硫黄系酸化防止剤
等を挙げることができ、これらは、通常、0.05〜
2.0重量%の割合で使用される。無灰清浄分散剤とし
ては、こはく酸イミド系、こはく酸アミド系、ベンジル
アミン系、こはく酸エステル系等があり、ホウ素含有無
灰清浄分散剤も使用できる。これらは、通常、0.05
〜7.0重量%の割合で使用される。金属清浄剤として
は、Ca−スルホネート、Mg−スルホネート、Ba−
スルホネート、Ca−フェネート、Mg−フェネート、
Ba−フェネート、Ca−サリシレート、Mg−サリシ
レート、Ba−サリシレート等があり、これらは、通
常、0.1〜5.0重量%の割合で使用される。腐食防
止剤としては、ベンゾトリアゾール、ベンゾトリアゾー
ル誘導体、チアジアゾール誘導体等があり、これらは、
通常0.01〜2.0重量%の割合で使用される。防錆
剤としては、カルボン酸、カルボン酸塩、スルホン酸
塩、アミン、アルケニルこはく酸又はその部分エステル
等が挙げられ、適宜添加することができる。消泡剤とし
ては、ジメチルポリシロキサン、ポリアクリレート等が
挙げられ、適宜添加することができる。
(3) Other additives In the hydraulic fluid composition for a shock absorber of the present invention, other additives, such as a friction modifier and an antiwear agent, may be added, if necessary, unless the object of the present invention is impaired. An antioxidant, an ashless detergent / dispersant, a metal detergent, a corrosion inhibitor, a rust inhibitor, an antifoaming agent, and the like can be appropriately added. Examples of the friction modifier include fatty acids (such as oleic acid and stearic acid), higher alcohols (such as oleyl alcohol), fatty acid esters, phosphate esters, phosphite esters, phosphate amine salts, oils and fats, polyhydric alcohol esters, Sorbitan esters, aliphatic amines and the like can be mentioned.
Usually, it is used in a proportion of 0.05 to 3.0% by weight. As antiwear agents, metal dithiophosphates (Zn, Pb, S
b, Mo, etc.), metal salts of dithiocarbamic acid (Zn, M
o etc.) Naphthenic acid metal salts (Pb etc.), fatty acid metal salts (Pb etc.), phosphate esters, phosphite esters, phosphate amine salts, sulfurized fats and oils, sulfur compounds, boron compounds, etc. , These are usually
It is used in a proportion of from 0.5 to 3.0% by weight. As antioxidants, alkylated diphenylamine, phenyl-α-
Amine antioxidants such as naphthylamine and alkylated phenyl-α-naphthylamine; phenolic antioxidants such as 2,6-di-t-butylphenol and 4,4′-methylenebis- (2,6-ditert-butylphenol) , Phosphite and other phosphorus antioxidants, dilauryl-
Sulfur-based antioxidants such as 3,3'-thiodipropionate and the like can be mentioned.
Used at a rate of 2.0% by weight. Examples of the ashless detergent / dispersant include succinimide-based, succinic amide-based, benzylamine-based and succinate-based detergents, and a boron-containing ashless detergent / dispersant can also be used. These are usually 0.05
It is used in a proportion of ~ 7.0% by weight. As the metal detergent, Ca-sulfonate, Mg-sulfonate, Ba-
Sulfonate, Ca-phenate, Mg-phenate,
There are Ba-phenate, Ca-salicylate, Mg-salicylate, Ba-salicylate and the like, which are usually used at a ratio of 0.1 to 5.0% by weight. Examples of the corrosion inhibitor include benzotriazole, benzotriazole derivatives, thiadiazole derivatives and the like.
Usually, it is used in a ratio of 0.01 to 2.0% by weight. Examples of the rust inhibitor include carboxylic acid, carboxylate, sulfonate, amine, alkenyl succinic acid and partial esters thereof, and the like can be added as appropriate. Examples of the antifoaming agent include dimethylpolysiloxane and polyacrylate, which can be added as appropriate.

【0020】(4)緩衝器用油圧作動油組成物 本発明の緩衝器用油圧作動油組成物は、減衰力安定性に
優れた、特に低温での乗り心地がよいものとするため
に、その粘度特性は、100℃における動粘度が1〜2
0mm/s、粘度指数が140以上であり、かつ、−
40℃におけるブルックフィールド(BF)粘度が20
00mPa・s以下である必要がある。好ましくは、1
00℃における動粘度が2〜8mm/s、粘度指数が
145以上であり、かつ、−40℃におけるブルックフ
ィールド粘度が1700mPa・s以下である。100
℃における動粘度が1mm/s未満の場合、蒸発量が
多くなり、また耐摩耗性が悪化し、一方、20mm
sを超えると低温粘度が大きくなりすぎる。粘度指数が
140未満の場合、低温粘度が大きくなりすぎる。−4
0℃におけるブルックフィールド粘度が2000mPa
・sを超えると低温における減衰力が大きくなり、乗り
心地や操縦安定性が悪くなる。
(4) Hydraulic oil composition for shock absorber The hydraulic oil composition for shock absorber of the present invention has excellent viscosity stability, especially its viscosity characteristics in order to provide good riding comfort at low temperatures. Has a kinematic viscosity at 100 ° C. of 1 to 2
0 mm 2 / s, a viscosity index of 140 or more, and −
Brookfield (BF) viscosity at 40 ° C. of 20
It is necessary to be not more than 00 mPa · s. Preferably, 1
The kinematic viscosity at 00 ° C is 2 to 8 mm 2 / s, the viscosity index is 145 or more, and the Brookfield viscosity at -40 ° C is 1700 mPa · s or less. 100
When the kinematic viscosity at 0 ° C is less than 1 mm 2 / s, the amount of evaporation increases and the abrasion resistance deteriorates, while 20 mm 2 / s
If it exceeds s, the low temperature viscosity becomes too large. When the viscosity index is less than 140, the low temperature viscosity becomes too large. -4
Brookfield viscosity at 0 ° C of 2000 mPa
If it exceeds s, the damping force at low temperatures becomes large, and the ride comfort and steering stability deteriorate.

【0021】[0021]

【実施例】以下に、実施例及び比較例を挙げて、本発明
についてさらに具体的に説明するが、本発明は、これら
の実施例のみに限定されるものではない。なお、実施例
におけるブルックフィールド粘度、蒸発性、剪断安定性
の各種物性の測定法は、下記の通りである。 (1)ブルックフィールド粘度 ASTM D2983に規定するブルックフィールド粘
度計により、−40℃におけるブルックフィールド(B
F)粘度を測定した。 (2)蒸発性 DIN51581に準拠して、温度120℃、3時間の
測定条件により、NOACK蒸発量を測定し、蒸発性を
評価した。 (3)剪断安定性 ASTM D2603に準拠して、試料に音波を照射し
て剪断を与え、照射前後の粘度から100℃における粘
度低下率を算出し、剪断安定性を評価した。その試験条
件は、試料30ml、音波出力10kHz、照射時間3
0分、循環水温度38℃とした。
The present invention will be described in more detail with reference to examples and comparative examples, but the present invention is not limited to these examples. The methods for measuring various physical properties of Brookfield viscosity, evaporability, and shear stability in Examples are as follows. (1) Brookfield Viscosity The Brookfield (B) at −40 ° C. was measured using a Brookfield viscometer specified in ASTM D2983.
F) The viscosity was measured. (2) Evaporability According to DIN51581, the NOACK evaporation amount was measured under the measurement conditions of a temperature of 120 ° C. and 3 hours, and the evaporability was evaluated. (3) Shear Stability According to ASTM D2603, a sample was irradiated with a sound wave to give shear, and the viscosity reduction rate at 100 ° C. was calculated from the viscosity before and after irradiation to evaluate the shear stability. The test conditions were as follows: sample 30 ml, sound wave output 10 kHz, irradiation time 3
The circulating water temperature was set to 38 ° C. for 0 minute.

【0022】[実施例1]潤滑油基油として、100℃
における動粘度が2.4mm/s、流動点が−35
℃、及び曇り点が−30℃以下である深脱蝋鉱油を用
い、添加剤として、組成物全量基準で、ポリメタクリレ
ート系粘度指数向上剤(重量平均分子量75,000)
4.0重量%、その他の添加剤として酸化防止剤、耐摩
耗剤等を必要な一定量添加して緩衝器用油圧作動油組成
物を調整した。ここで得られた緩衝器用油圧作動油組成
物の粘度特性、粘度指数、蒸発性及び剪断安定性を測定
し、評価した。結果を表1に示す。実施例1の緩衝器用
油圧作動油組成物は、その粘度特性は、100℃におけ
る動粘度が3.1mm/s、粘度指数が149であ
り、かつ、−40℃におけるブルックフィールド粘度が
1650mPa・sであり、蒸発性は、NOACK蒸発
量が4.3重量%、剪断安定性は、音波法粘度低下率が
4.0%であり、良好であつた。
Example 1 100 ° C. as lubricating base oil
Has a kinematic viscosity of 2.4 mm 2 / s and a pour point of −35.
C. and a deep dewaxed mineral oil having a cloud point of -30.degree. C. or lower, and as an additive, a polymethacrylate-based viscosity index improver (weight average molecular weight 75,000) based on the total amount of the composition.
A required amount of 4.0% by weight and other additives such as an antioxidant and an antiwear agent was added to prepare a hydraulic oil composition for a shock absorber. The viscosity characteristics, viscosity index, evaporability, and shear stability of the hydraulic oil composition for a shock absorber obtained here were measured and evaluated. Table 1 shows the results. The hydraulic fluid composition for a shock absorber of Example 1 has a viscosity characteristic of a kinematic viscosity at 100 ° C. of 3.1 mm 2 / s, a viscosity index of 149, and a Brookfield viscosity at −40 ° C. of 1650 mPa · s. As for the evaporating property, the NOACK evaporation amount was 4.3% by weight, and the shear stability was good because the sonication method viscosity reduction rate was 4.0%.

【0023】[0023]

【表1】 [Table 1]

【0024】[実施例2〜8]表1に示す潤滑油基油成
分と粘度指数向上剤及びその他の添加剤成分を同表に示
す割合で配合し、緩衝器用油圧作動油組成物を調製し
た。基油の配合割合は、基油全量基準であり、粘度指数
向上剤とその他の添加剤の添加割合は、組成物全量基準
である。実施例2〜8に示す緩衝器用油圧作動油組成物
の粘度特性、粘度指数、蒸発性及び剪断安定性を測定
し、評価した。結果を表1に示す。いずれの実施例にお
いても、緩衝器用油圧作動油として高品質のものが得ら
れることが明らかになった。
Examples 2 to 8 The lubricating base oil components shown in Table 1 were mixed with the viscosity index improver and other additive components in the proportions shown in the table to prepare hydraulic oil compositions for shock absorbers. . The mixing ratio of the base oil is based on the total amount of the base oil, and the adding ratio of the viscosity index improver and other additives is based on the total amount of the composition. The viscosity characteristics, viscosity index, evaporability and shear stability of the hydraulic fluid compositions for shock absorbers shown in Examples 2 to 8 were measured and evaluated. Table 1 shows the results. In any of the examples, it was found that high quality hydraulic oil for shock absorbers could be obtained.

【0025】[比較例1〜4]表1に示す潤滑油基油成
分と各種添加剤成分を同表に示す割合で配合し、緩衝器
用油圧作動油組成物を調製した。比較例1は、基油とし
て、深脱蝋鉱油を用いないで、通常の溶剤脱蝋鉱油(流
動点−15℃、100℃動粘度2.7mm/s)を用
い、組成物全量基準で、ポリメタクリレート系粘度指数
向上剤(重量平均分子量45,000)1.5重量%等
を配合した場合であるが、その結果、−40℃のブルッ
クフィールド粘度が4700mPa・sであり、低温粘
度特性が悪い。比較例2は、基油として、100℃にお
ける動粘度が2.4mm/sの深脱蝋鉱油を用い、組
成物全量基準で、ポリメタクリレート系粘度指数向上剤
(重量平均分子量75,000)21.0重量%等を配
合した場合であるが、低温粘度が2000mPa・sを
超え、かつ剪断安定性も悪い。比較例3は、基油とし
て、ポリα−オレフィンとエステル化合物との合成油を
用い、組成物全量基準で、ポリメタクリレート系粘度指
数向上剤(重量平均分子量100,000)26.0重
量%等を配合して、100℃における動粘度を20.2
mm/sとした場合であるが、低温粘度が2000m
Pa・sを超え、かつ剪断安定性も悪い。比較例4は、
基油として、基油全量基準で、100℃における動粘度
が2.4mm/sの深脱蝋鉱油70重量%に、40℃
における動粘度が1.8mm/sの低粘度鉱油30重
量%を混合して用い、組成物全量基準で、ポリメタクリ
レート系粘度指数向上剤(重量平均分子量75,00
0)15.0重量%等を配合した場合であるが、低温粘
度特性は良好なもののNOACK蒸発量は、明らかに悪
化するとともに剪断安定性も悪くなる。
[Comparative Examples 1 to 4] Lubricating base oil components and various additive components shown in Table 1 were blended in the proportions shown in the same table to prepare hydraulic working oil compositions for shock absorbers. Comparative Example 1 used a normal solvent dewaxed mineral oil (pour point -15 ° C, 100 ° C kinematic viscosity 2.7 mm 2 / s) without using a deeply dewaxed mineral oil as a base oil, and based on the total amount of the composition. And 1.5 wt% of a polymethacrylate-based viscosity index improver (weight average molecular weight: 45,000). As a result, the Brookfield viscosity at −40 ° C. is 4700 mPa · s, and the low-temperature viscosity characteristic is low. Is bad. Comparative Example 2 used a deep dewaxed mineral oil having a kinematic viscosity at 100 ° C. of 2.4 mm 2 / s as a base oil, and based on the total amount of the composition, a polymethacrylate-based viscosity index improver (weight average molecular weight 75,000). In the case where 21.0% by weight or the like is blended, the low-temperature viscosity exceeds 2000 mPa · s and the shear stability is poor. Comparative Example 3 used a synthetic oil of a poly-α-olefin and an ester compound as a base oil, and used a polymethacrylate-based viscosity index improver (weight average molecular weight of 100,000) 26.0% by weight based on the total amount of the composition. And a kinematic viscosity at 100 ° C. of 20.2
mm 2 / s, but the low-temperature viscosity is 2000 m
Exceeds Pa · s and has poor shear stability. Comparative Example 4
As a base oil, 70% by weight of a deep-dewaxed mineral oil having a kinematic viscosity at 100 ° C. of 2.4 mm 2 / s based on the total amount of the base oil was converted to
And 30% by weight of a low-viscosity mineral oil having a kinematic viscosity of 1.8 mm 2 / s, and a polymethacrylate-based viscosity index improver (weight-average molecular weight of 75,000
0) 15.0% by weight or the like is blended. Although the low-temperature viscosity characteristics are good, the NOACK evaporation amount is clearly deteriorated and the shear stability is also deteriorated.

【0026】[0026]

【発明の効果】本発明の緩衝器用油圧作動油組成物は、
特定性状の深脱蝋鉱油、及び/又は特定性状の合成油の
基油に、粘度指数向上剤及び/又は流動点降下剤を特定
量配合し、しかも緩衝器用油圧作動油の100℃におけ
る動粘度、粘度指数、かつ−40℃におけるブルックフ
ィールド粘度を特定範囲内にすることにより、緩衝器用
油圧作動油として要求される低温粘度特性、蒸発性、及
び剪断安定性に優れ、特に高温から低温に渡って減衰力
安定性に優れている。
The hydraulic fluid composition for a shock absorber according to the present invention comprises:
A specific amount of a viscosity index improver and / or a pour point depressant is blended with a base oil of a deep-dewaxed mineral oil having a specific property and / or a synthetic oil having a specific property, and the kinematic viscosity at 100 ° C. of a hydraulic fluid for a shock absorber. , Viscosity index, and Brookfield viscosity at −40 ° C. within the specified ranges, thereby exhibiting excellent low-temperature viscosity characteristics, evaporability, and shear stability required for hydraulic fluids for shock absorbers, and particularly from high to low temperatures. And excellent damping force stability.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C10M 145:14) C10N 30:02 30:06 30:08 40:08 (72)発明者 大塚 直登 埼玉県入間郡大井町西鶴ヶ岡一丁目3番1 号 東燃株式会社総合研究所内 Fターム(参考) 4H104 BA07A BB33A BB34A CA05A DA02A EA02A EA02Z EA04A EB02 EB05 LA01 LA03 LA04 LA20 PA05 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C10M 145: 14) C10N 30:02 30:06 30:08 40:08 (72) Inventor Naoto Otsuka Saitama 1-3-1 Nishi-Tsurugaoka, Oi-machi, Iruma-gun F-term in Tonen Research Laboratory (reference) 4H104 BA07A BB33A BB34A CA05A DA02A EA02A EA02Z EA04A EB02 EB05 LA01 LA03 LA04 LA20 PA05

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 下記の鉱油(A)及び/又は合成油
(B)からなる基油に、組成物全量を基準として20重
量%以下の粘度指数向上剤及び/又は流動点降下剤を配
合してなる緩衝器用油圧作動油組成物であって、 その粘度特性は、100℃における動粘度が1〜20m
/s、粘度指数が140以上であり、かつ、−40
℃におけるブルックフィールド粘度が2000mPa・
s以下であることを特徴とする緩衝器用油圧作動油組成
物。 鉱油(A):100℃における動粘度が2〜3mm
s、流動点が−30℃以下、及び曇り点が−27.5℃
以下である深脱蝋鉱油(a)、又は該深脱蝋鉱油(a)
と、40℃における動粘度が1.0〜6.0mm/s
である低粘度鉱油(b)との混合鉱油(ただし、該低粘
度鉱油(b)の含有量は、混合鉱油全量を基準として2
0重量%未満である)。 合成油(B):100℃における動粘度が1.5〜45
mm/sであるポリα−オレフィン(c)、及び/又
は100℃における動粘度が1.5〜20mm /s及
び流動点が−30℃以下であるエステル化合物(d)。
1. The following mineral oil (A) and / or synthetic oil
20 bases on the base oil consisting of (B) based on the total amount of the composition
% Or less of a viscosity index improver and / or a pour point depressant.
A hydraulic oil composition for a shock absorber, comprising a kinematic viscosity at 100 ° C. of 1 to 20 m.
m2/ S, a viscosity index of 140 or more, and -40
Brookfield viscosity at 2000C
s or less, the hydraulic fluid composition for a shock absorber
object. Mineral oil (A): kinematic viscosity at 100 ° C. is 2 to 3 mm2/
s, pour point of -30 ° C or less, and cloud point of -27.5 ° C
Or a deeply dewaxed mineral oil (a), or
And the kinematic viscosity at 40 ° C. is 1.0 to 6.0 mm2/ S
Mineral oil mixed with a low-viscosity mineral oil (b)
The mineral oil (b) content is 2% based on the total amount of the mixed mineral oil.
Less than 0% by weight). Synthetic oil (B): kinematic viscosity at 100 ° C. is 1.5 to 45.
mm2/ S of poly-α-olefin (c), and / or
Is a kinematic viscosity at 100 ° C. of 1.5 to 20 mm 2/ S and
And an ester compound (d) having a pour point of -30 ° C or lower.
JP10287958A 1997-02-10 1998-10-09 Hydraulic oil composition for buffer Pending JP2000109876A (en)

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SG9904835A SG108213A1 (en) 1998-10-09 1999-09-24 Hydraulic oil composition for shock absorbers
CA002284343A CA2284343A1 (en) 1998-10-09 1999-10-01 Hydraulic oil composition for shock absorbers
EP99307976A EP0992570A3 (en) 1998-10-09 1999-10-08 Hydraulic oil composition for shock absorbers
US10/682,545 US7078391B2 (en) 1997-02-10 2003-10-08 Method of treating edematous retinal disorders

Applications Claiming Priority (1)

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Publication Number Publication Date
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ID=17723955

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US20040176256A1 (en) * 2002-11-07 2004-09-09 Nippon Oil Corporation Lubricating oil composition for transmissions
US7585823B2 (en) 2003-09-13 2009-09-08 Exxonmobil Chemical Patents Inc. Lubricating fluids with enhanced energy efficiency and durability
DE102004015792A1 (en) * 2004-03-29 2005-10-20 Bantleon Hermann Gmbh Synthetic lubricant composition and its use
US7759293B2 (en) * 2004-11-22 2010-07-20 Nippon Oil Corporation Hydraulic oil composition for shock absorbers
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WO2012076285A1 (en) 2010-12-10 2012-06-14 Evonik Rohmax Additives Gmbh A lubricant composition
CN108329979A (en) * 2018-01-20 2018-07-27 盘锦北方沥青股份有限公司 A kind of long-life energy-saving hydraulic oil and preparation method thereof
US20230134730A1 (en) * 2020-04-30 2023-05-04 Eneos Corporation Refrigerating machine oil, working fluid composition for refrigerating machine, and method for producing refrigerating machine oil
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Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4776967A (en) * 1987-02-27 1988-10-11 Idemitsu Kosan Company Limited Lubricating oil composition
JP2573948B2 (en) * 1987-05-14 1997-01-22 出光興産 株式会社 Lubricating oil composition for machinery with orifice mechanism
US5646099A (en) * 1995-07-17 1997-07-08 Exxon Chemical Patents Inc. Automatic transmission fluids of improved viscometric properties
US5641732A (en) * 1995-07-17 1997-06-24 Exxon Chemical Patents Inc. Automatic transmission fluids of improved viscometric properties

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WO2008123249A1 (en) 2007-03-30 2008-10-16 Nippon Oil Corporation Operating oil for buffer
US8603953B2 (en) 2007-03-30 2013-12-10 Jx Nippon Oil & Energy Corporation Operating oil for buffer
JP2010531921A (en) * 2007-06-28 2010-09-30 シェブロン ユー.エス.エー. インコーポレイテッド Power steering fluid
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US9688941B2 (en) 2013-08-23 2017-06-27 Idemitsu Kosan Co., Ltd. Lubricating oil composition for shock absorber

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