JP3211959B2 - Lubricant or lubricant concentrate - Google Patents

Lubricant or lubricant concentrate

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Publication number
JP3211959B2
JP3211959B2 JP50365188A JP50365188A JP3211959B2 JP 3211959 B2 JP3211959 B2 JP 3211959B2 JP 50365188 A JP50365188 A JP 50365188A JP 50365188 A JP50365188 A JP 50365188A JP 3211959 B2 JP3211959 B2 JP 3211959B2
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Japan
Prior art keywords
lubricant
group
component
weight
mpa
Prior art date
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JP50365188A
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Japanese (ja)
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JPH01503545A (en
Inventor
フロエシュマン,エラスムス
Original Assignee
マックス グリル ゲゼルシャフト ミット ベシュレンクテル
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Publication of JPH01503545A publication Critical patent/JPH01503545A/en
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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
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • C10M169/044Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/02Petroleum fractions
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/04Fatty oil fractions
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/02Well-defined hydrocarbons
    • C10M105/06Well-defined hydrocarbons aromatic
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/18Ethers, e.g. epoxides
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/36Esters of polycarboxylic acids
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/38Esters of polyhydroxy compounds
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    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
    • C10M107/08Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation containing butene
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    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/22Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/28Macromolecular 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
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    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/30Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/32Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
    • C10M107/34Polyoxyalkylenes
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    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/16Ethers
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    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/12Thio-acids; Thiocyanates; Derivatives thereof
    • C10M135/14Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
    • C10M135/18Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond thiocarbamic type, e.g. containing the groups
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    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/32Heterocyclic sulfur, selenium or tellurium compounds
    • C10M135/36Heterocyclic sulfur, selenium or tellurium compounds the ring containing sulfur and carbon with nitrogen or oxygen
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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
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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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    • C10M141/00Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/10Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
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    • 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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    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic compounds
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
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    • C10M2203/065Well-defined aromatic compounds used as base material
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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Lubricants (AREA)

Abstract

A lubricant or lubricant concentrate based on mineral and/or synthetic oil with improved lubricating properties, in particular improved load-bearing, sliding and anticorrosion properties, contains a) one or more mineral and/or synthetic oils as the basic oil, b) at least one quadrivalent to octavalent alcohol with at least one quaternary carbon atom and at least one ether bond per molecule and having a density d20 of at least 0.900 and an enthalpy H of at least 350 kcal/kg, c) at least one asymmetric organaometallic compound, d) at least one phosphorus carrier, and e) at least one sulphur carrier, as well as f) other usual additives.

Description

【発明の詳細な説明】 本発明は潤滑剤が改善された、特に腐食防止性と同様
に耐荷重性、滑動性が改善された鉱油及び/又は合成油
に基づく新規の潤滑剤又は潤滑剤濃縮物に関する。
The present invention relates to novel lubricants or lubricant concentrates based on mineral and / or synthetic oils with improved lubricants, in particular with improved load-bearing, sliding properties as well as corrosion protection. About things.

去る10年間の間に多数の過程及び潤滑システムが運転
中の機械部品の摩擦及び摩耗を減少し、エネルギー及び
取替え部品の費用を低減し、更に潤滑剤及び材料の耐用
年数を伸ばすために開発されてきた。運転中の機械部品
の全使用期間において効果的である潤滑剤(以下、「終
生潤滑剤」という)は、ますます制限的になっている生
態学的な面からの要請を考慮すると、理想的な潤滑剤で
あると考えられる。
During the last decade, numerous processes and lubrication systems have been developed to reduce the friction and wear of operating machine parts, reduce the cost of energy and replacement parts, and extend the useful life of lubricants and materials. Have been. Lubricants that are effective during the entire life of a machine component in operation (hereinafter “lifetime lubricants”) are ideal in view of the increasingly restrictive ecological requirements. It is considered to be a good lubricant.

長寿命で高機械効率の潤滑剤、潤滑システム及び潤滑
過程への途中で、第1段階においていわゆる化学的摩耗
潤滑剤が開発された。それを使用することによつて、表
面上に化学的に反応性のおおいの被覆を形成することに
より又は潤滑剤基礎主成分中に化学的に反応性の化合物
を導入することにより運転中の部品の微小な山(microm
ountain)の表面上に塩を生成することによつて金属と
金属の接触は大きく妨げられる。この方法で機械部品の
シージングを防ぐことができる。しかし同時にお互いに
対して動く金属部品間の塩被覆のせん断による摩耗は促
進された。それゆえ材料の耐用年数は比較的短かいまま
である。さらに進んだ段階において、潤滑するおおい被
覆、懸濁物、ペースト又は脂肪の形で導入される、黒
鉛、MoS2、TiO2、Ca3(PO4、テフロンなどのような
運転中の金属部品間に導入される固体潤滑剤が開発され
た。この方法において摩擦された部品はお互いからより
よく分離され耐負荷性は増大した。しかしながら、高い
周速の求心的な動きの影響のもとで、その相違する特定
の密度により高い温度で固体潤滑剤と基礎媒材は遅かれ
早かれお互いに分離される。長命の潤滑はそれによつて
限定される。さらに進んだ段階において運転中に潤滑剤
中に溶解した化学的錯体から適切な金属カチオンの摩擦
表面上への析出が達成された。摩擦する部品の圧力と温
度のもとでそれらは金属境界層と共に共晶を形成し、そ
れはでこぼこの谷間をなめらかになるように満たし、そ
してでこぼこの最高点を一部摩擦化学的に一部微小可塑
的に平らにする。有機金属化合物のアニオン部分は新し
く再構築された共晶摩擦面上にもとの位置に潤滑剤とし
て働きまた粘着する反応層を形成する。
On the way to long life, high mechanical efficiency lubricants, lubrication systems and lubrication processes, so-called chemical wear lubricants were developed in the first phase. Parts in operation by using it, by forming a chemically reactive coating on the surface or by introducing a chemically reactive compound into the lubricant base component. Microm of mountain (microm
The formation of salts on the surface of the ountain greatly hinders metal-to-metal contact. In this way, sheathing of mechanical parts can be prevented. At the same time, however, wear due to shearing of the salt coating between the metal parts moving relative to each other was promoted. Therefore, the service life of the material remains relatively short. In a further stage, operating metals such as graphite, MoS 2 , TiO 2 , Ca 3 (PO 4 ) 2 , Teflon, etc., which are introduced in the form of lubricating sheathings, suspensions, pastes or fats Solid lubricants introduced between parts have been developed. In this way, the rubbed parts were better separated from each other and the load carrying capacity was increased. However, under the influence of high peripheral speed centripetal movement, the solid lubricant and the base medium are sooner or later separated from each other at higher temperatures due to their different specific densities. Long-life lubrication is thereby limited. In a further step, the deposition of the appropriate metal cations on the friction surface from the chemical complex dissolved in the lubricant during operation was achieved. Under the pressure and temperature of the parts to be rubbed, they form a eutectic with the metallic boundary layer, which fills the uneven valleys smoothly and partially tribochemically Flatten plastically. The anionic portion of the organometallic compound acts as a lubricant on the newly reconstructed eutectic friction surface at the original location and forms a sticky reaction layer.

長すぎる初期段階、高すぎる摩耗係数及び摩耗のほか
に、反応の進行の制御はこれらの潤滑システムに関する
問題である。狭い嵌合における製品調整のために微小の
凹凸を除去するための薬剤としてもはや十分に機能しな
い、材料と関係のない共晶及び反応層が形成されると、
この場所において過負荷となる領域が生じ、結果として
後に摺動面において金属の破損が生じるか、若しくは、
有機金属化合物の活性成分が強化され、化学的摩耗潤滑
相に速すぎる除去速度及び短すぎる耐用期間を与える結
果になる。
Control of the progress of the reaction, besides too long an initial stage, too high abrasion coefficient and wear, is a problem with these lubrication systems. When a eutectic and reaction layer unrelated to the material is formed, which no longer functions well as an agent for removing microscopic irregularities for product adjustment in a narrow fit,
An overloaded area occurs at this location, resulting in subsequent metal damage on the sliding surface, or
The active component of the organometallic compound is strengthened, resulting in the chemical wear lubricating phase having too fast removal rates and too short a service life.

たとえば、DE−PS941 678から五硫化リンの溶けやす
い反応生成物又は液体もしくは固体の脂肪族炭化水素も
しくはテルペン炭化水素の中身を有する潤滑油がわか
る。DE−PS923 984からスルホン酸亜鉛と組み合つて金
属含有アルキルフエノールスルフイドエステルを含有す
る潤滑油を知る。DE−AS1444892から芳香族亜鉛ジチオ
フオスフアートの塩及び亜鉛カルボン酸塩を水の存在下
に含有する潤滑油を知る。先に述べた両方の製品は潤滑
油洗浄剤であるが後の製品は銀のベアリング表面の腐食
を防止するといわれる。DE−AS1296730から任意にアル
キル化又はエステル化リン酸の塩と一緒に置換コハク酸
を含有する潤滑油を知る。この製品は洗浄剤として酸化
防止剤の機能がある。DE−AS1271878からジチオフオス
フアートとジチオフオスフイナート塩の組み合せを知
る。DE−OS1594555から遊離の硫黄、ジアルキルジチオ
フオスフアート及び塩素化炭化水素を含有する切削油を
知る。US−PS3462367に亜鉛又はアンチモンジチオカル
バメートを含有する潤滑油が開示されている。US−PS27
58087から高温で五硫化リンとオレフインを反応させて
調製した硫黄−リン−化合物、及びフタル酸亜鉛を含有
する潤滑油がわかる。しかしながら、これら既知のすべ
ての潤滑油添加物は今日の要求を満たさなく、特にそれ
らは潤滑箇所の領域に重質の酸化物の析出を引き起し、
またあまりにも高い摩耗を引き起す。
For example, DE-PS 941 678 describes soluble reaction products of phosphorus pentasulfide or lubricating oils having a liquid or solid aliphatic or terpene hydrocarbon content. DE-PS 923 984 discloses lubricating oils containing metal-containing alkylphenol sulfide esters in combination with zinc sulfonates. DE-AS 144 489 2 discloses a lubricating oil containing a salt of an aromatic zinc dithiophenophthalate and a zinc carboxylate in the presence of water. Both products mentioned above are lubricating oil cleaners, while later products are said to prevent corrosion of silver bearing surfaces. DE-AS1296730 discloses lubricating oils containing substituted succinic acids, optionally together with salts of alkylated or esterified phosphoric acids. This product has an antioxidant function as a cleaning agent. From DE-AS1271878, learn the combination of dithiophenosphate and dithiophene osfinate. From DE-OS 1 594 555 we know cutting oils containing free sulfur, dialkyldithiophenosphate and chlorinated hydrocarbons. US-PS3462367 discloses lubricating oils containing zinc or antimony dithiocarbamate. US-PS27
58087 shows a sulfur-phosphorus compound prepared by reacting phosphorus pentasulfide and olefin at high temperature, and a lubricating oil containing zinc phthalate. However, all these known lubricating oil additives do not meet today's requirements, in particular they cause heavy oxide precipitation in the area of the lubricating points,
It also causes too high abrasion.

US−PS2734865から硫化リン、獣脂油脂肪酸アルコー
ルエステル、塩化亜鉛及び水酸化バリウムの複合反応生
成物と結合してアルカリ土類金属塩のジチオフオスフア
ートの形成される潤滑油添加剤を使用することがわか
る。それによつて達成される摩擦係数及び摩耗値は今日
の要求に対しあまりに高過ぎ、さらに面圧力の値はあま
りに低すぎる。US−PS2734864から硫化リン、羊脂及び
アルコールエステルの複合反応生成物と結合してアルカ
リ土類金属のジチオフオスフアートの形成される潤滑油
添加剤がわかる。限定されない生成物は十分な量のバリ
ウム及び亜鉛を含有する。そのような潤滑油添加剤は我
慢のできない臭いのために実際に使用できなく、またそ
れと接触して受ける作業員の健康を危険にさらす。DE−
PS1954452から鉱油及び合成油に基礎を置く潤滑剤は鉱
油又は合成油のほかに添加剤として10〜18個の炭素原子
を有するエポキシ化脂肪酸と1価または多価アルコール
のエステル、亜鉛、鉛、スズ、タングステン、モリブデ
ン、ニオビウム又はランタンのアルキル、アラルキル又
はアラールジチオフオスフアート、及び任意に硫黄・リ
ン・化合物を含有することがわかる。DE−PS2108780か
ら鉱油又は合成油に基礎を置く潤滑剤及び潤滑剤濃縮物
は、それぞれ、アルキル、アリール又はアラルキル基で
エステル化された鉛、タングステン、モリブデン及び/
又はバナジウムジチオフオスフアートのほかに少なくと
も1種類の亜鉛ジアルキルジチオフオスフアート化合物
及び金属を含まない硫黄・リン・化合物を含有すること
がわかる。またこれら後の広範囲に及ぶ用途を見出した
潤滑剤は、現代の長寿命で高機械効率の潤滑剤に関する
すべての要求をもはや満たさない。それらの摩擦係数及
び摩耗はあまりにも高く、その貯蔵抵抗は不十分であ
り、その長期間使用は潤滑剤分野あまりにも高い再生分
担分を導く。
Use of a lubricating oil additive from US-PS2734865 which combines with the combined reaction product of phosphorus sulfide, tallow oil fatty acid alcohol ester, zinc chloride and barium hydroxide to form a dithiophenophthalate of an alkaline earth metal salt I understand. The coefficient of friction and wear values achieved thereby are too high for today's requirements, and the values of the surface pressure are too low. US-PS 2734864 describes lubricating oil additives which combine with the complex reaction product of phosphorus sulphide, mutton and alcohol esters to form an alkaline earth metal dithiophenophthalate. Non-limiting products contain sufficient amounts of barium and zinc. Such lubricating oil additives are practically unusable due to intolerable odors and also endanger the health of workers who come into contact with them. DE−
Lubricants based on mineral and synthetic oils from PS1954452 include mineral or synthetic oils, as additives, esters of epoxidized fatty acids with 10 to 18 carbon atoms and monohydric or polyhydric alcohols, zinc, lead, tin , Tungsten, molybdenum, niobium or lanthanum alkyl, aralkyl or aralkyldithiophenate, and optionally sulfur-phosphorus compounds. Lubricants and lubricant concentrates based on mineral or synthetic oils from DE-PS 2108780 are, respectively, lead, tungsten, molybdenum and / or esterified with alkyl, aryl or aralkyl groups.
Alternatively, it is found that in addition to vanadium dithiophenophthalate, at least one kind of zinc dialkyldithiophenophthalate compound and a metal-free sulfur-phosphorus-containing compound are contained. Also, lubricants that have found widespread use in these later years no longer meet all the requirements for modern long-life, high-mechanical-efficiency lubricants. Their coefficient of friction and wear are too high, their storage resistance is inadequate and their long-term use leads to too high a share of regeneration in the lubricant sector.

本発明の目的は潤滑性が改善された、特に摩擦及び摩
耗性が改善され、またエネルギー及び取り替え部品に関
する必要性をはつきりと減少し、そして最高の要求を満
たす鉱油又は合成油に基礎を置く新規の潤滑剤又は潤滑
剤濃縮物を提供することにある。
It is an object of the present invention to improve the lubricating properties, especially the friction and wear properties, to reduce the need for energy and replacement parts, and to build on mineral or synthetic oils meeting the highest requirements. It is to provide a new lubricant or lubricant concentrate.

本発明によるこの目的は、驚くべきことに通常の添加
剤のほかに鉱油及び/又は合成油にその分子中に少なく
とも1個の第4級炭素原子及び少なくとも1個のエーテ
ル結合を含有し、そして少なくとも0.900の密度d20及び
少なくとも350Kcal/Kgのエンタンピーを有する少なくと
も1種類の4価〜8価のアルコール、少なくとも1種類
の不斉有機金属化合物、少なくとも1種類のリン含有物
質及び少なくとも1種類の硫黄含有物質を添加すること
によつて達成することができる。
This object according to the invention is surprising in that, besides the usual additives, mineral oils and / or synthetic oils contain at least one quaternary carbon atom and at least one ether linkage in their molecules, and at least one tetravalent to octavalent alcohol having Entanpi density d 20 and at least 350 kcal / Kg of at least 0.900, at least one asymmetric organometallic compound, at least one phosphorus-containing material and at least one sulfur This can be achieved by adding contained substances.

本発明の主題は鉱油及び/又は合成油に基礎を置く新
規な潤滑剤又は潤滑剤濃縮物であつて、 a) 基油として1種又はそれ以上の鉱油及び/又は合
成油、並びに b) その分子中に少なくとも1個のエーテル結合だけ
でなく少なくとも1個の第4級炭素原子を有し、そして
少なくとも0.900の密度d20及び少なくとも350Kcal/Kgの
エンタルピーHを有する少なくとも1種類の4価〜8価
のアルコール、 c) 少なくとも1種類の不斉有機金属化合物、 d) 少なくとも1種類のリン含有物質、 e) 少なくとも1種類の硫黄含有物質及び f) さらにまた通常の添加剤 を含有することを特徴とする。
The subject of the present invention is a novel lubricant or lubricant concentrate based on mineral and / or synthetic oils, comprising: a) one or more mineral and / or synthetic oils as base oil; having at least one quaternary carbon atom not only at least one ether linkage in the molecule, and at least one tetravalent having enthalpy H of density d 20 and at least 350 kcal / Kg of at least 0.900 to 8 C) at least one asymmetric organometallic compound, d) at least one phosphorus-containing substance, e) at least one sulfur-containing substance, and f) also characterized by the usual additives And

本発明の潤滑剤及び潤滑剤濃縮物は、特にその摩擦及
び摩耗性並びにエネルギー及び取り替え部品に関する必
要性を実質的に減少することに関して既知の潤滑剤及び
潤滑剤濃縮物より優れている。このことは、摩擦及び摺
動領域に本発明の潤滑剤及び潤滑剤濃縮物を使用するこ
とにより、無定形の固体化された金属溶融物から成るガ
ラス表面のような金属表面が形成され、その表面が何れ
かの金属の結晶構造も示していないという事実によると
思われる。本発明の潤滑剤又は潤滑剤濃縮物を使用する
ことによつて形成されると信じられるガラス状の円滑な
摩擦及び滑走表面は、摩擦係数及び摩耗、酸化及び腐食
が実質的に減少されるから全体の潤滑過程を改善する。
またいわゆる嵌合関係により生じる錆び(fitting rus
t)は本発明の潤滑剤及び潤滑剤濃縮物によつて防止さ
れる。その上、本発明の潤滑剤及び潤滑剤濃縮物はどの
ような鉛も、硫黄含有まつこう鯨油も、またほとんどリ
ンを含有しないから非汚染性である。このことは本発明
の潤滑剤及び潤滑剤濃縮物について行なつた魚の試験及
び細菌培養試験で証明された。その上、それらは通常の
土壌中で3〜4ケ月以内に60%程度まで生物学的に分解
される。
The lubricants and lubricant concentrates of the present invention are superior to known lubricants and lubricant concentrates, particularly with regard to their friction and wear properties and substantially reducing energy and the need for replacement parts. This means that the use of the lubricants and lubricant concentrates of the present invention in the friction and sliding areas results in the formation of a metal surface, such as a glass surface made of an amorphous solidified metal melt. This is probably due to the fact that the surface does not show the crystal structure of any metal. The glassy smooth friction and gliding surfaces believed to be formed by using the lubricants or lubricant concentrates of the present invention provide a substantially reduced coefficient of friction and abrasion, oxidation and corrosion. Improve the overall lubrication process.
Also, rust caused by the so-called mating relationship (fitting rus)
t) is prevented by the lubricants and lubricant concentrates of the present invention. In addition, the lubricants and lubricant concentrates of the present invention are non-polluting because they contain no lead, no sulfur-containing pepper oil and little phosphorus. This has been demonstrated in fish tests and bacterial culture tests performed on the lubricants and lubricant concentrates of the present invention. Moreover, they are biologically degraded in normal soil to as much as 60% within 3-4 months.

このように、本発明の潤滑剤及び潤滑剤濃縮物は、非
常に非汚染性であるとみなすことができ、特に、これら
は自動車の等速ジョイント(homokinetic joints)、す
なわち高速回転及び高負荷を受ける小さなジョイントに
おいて使用されるのに適している。そして、本発明の潤
滑剤及び潤滑剤濃縮物は、他の全ての既知の潤滑剤より
理想的な潤滑剤、すなわち“終生潤滑剤”により近いも
のである。その上、本発明に従つて使用される第4級炭
素原子を持つポリエーテル化合物は意味のある熱安定性
を有し、また300℃までの高温運転へ利用することを可
能にする。それらは高い機械効率のエンジン、タービ
ン、ローラーベアリング、同調継手及びその他の高い機
械効率の機械要素と終生潤滑としてそれらを使用するた
めの可能性を提供する。
Thus, the lubricants and lubricant concentrates of the present invention can be considered to be very non-polluting, in particular, they can reduce the homokinetic joints of motor vehicles, i.e. high speed rotation and high loads. Suitable for use in receiving small joints. And the lubricants and lubricant concentrates of the present invention are closer to ideal lubricants, or "lifetime lubricants", than all other known lubricants. Moreover, the polyether compounds with quaternary carbon atoms used according to the invention have significant thermal stability and make them available for high-temperature operation up to 300 ° C. They offer the possibility of using them as high mechanical efficiency engines, turbines, roller bearings, tuning joints and other high mechanical efficiency mechanical elements and life-long lubrication.

本出願に使用された“鉱油及び/又は合成油に基礎を
置く潤滑剤又は潤滑剤濃縮物”は鉱油及び/又は合成油
に基礎を置く潤滑脂肪だけでなく潤滑油を含むことを意
味する。
As used herein, "lubricants or lubricant concentrates based on mineral and / or synthetic oils" are meant to include lubricating oils as well as lubricating fats based on mineral and / or synthetic oils.

ここに使用された“第4級炭素原子含有化合物”は分
子当り4価の少なくとも1個の炭素原子がおのおの4個
の炭素原子によつて置換される化合物を含むことを意味
する。そのような化合物の実例は単量体の、二量体の及
び三量体のペンタエリスリトールエーテル、別のポリオ
ールエーテル、ペンタエリスリトールエトキシエーテル
だけでなくテロメル酸ペンタエリスリトールエーテル及
び相当するエトキシル化エーテルである。
As used herein, "quaternary carbon atom-containing compound" is meant to include compounds in which at least one tetravalent carbon atom per molecule is replaced by each four carbon atoms. Illustrative of such compounds are the monomeric, dimeric and trimeric pentaerythritol ethers, another polyol ether, pentaerythritol ethoxy ether as well as pentaerythritol ether telomerate and the corresponding ethoxylated ether. .

以下の実施例からわかるように本発明の潤滑剤及び潤
滑剤濃縮物は、既知の潤滑剤及び潤滑剤濃縮物に比べて
実質的に改善された性質を有する。本発明の潤滑剤によ
つて形成されるガラス状の円滑な摩擦及び滑走面は駆動
エネルギーを節約し、また本質的に摩擦係数を低下し、
そしてまた非常に良好な粘着性の境界潤滑フイルムの形
成によつてそれはまた点状負荷と弾性的流体力学的潤滑
を可能にする。このことは潤滑剤と潤滑された場所の摩
擦温度の低下を生じ、両方の酸化抵抗の延長を生じそし
て金属摩擦のパートナーは明確な荷重変化及び温度応力
を少ししか受けない。
As can be seen from the examples below, the lubricants and lubricant concentrates of the present invention have substantially improved properties as compared to known lubricants and lubricant concentrates. The glassy smooth friction and running surface formed by the lubricant of the present invention saves driving energy and also inherently reduces the coefficient of friction,
And also by virtue of the formation of a very good sticky boundary lubricating film, it also enables point loads and elastic hydrodynamic lubrication. This results in a decrease in the friction temperature of the lubricant and the lubricated area, an increase in both oxidation resistances, and the metal friction partner undergoes less pronounced load changes and thermal stresses.

要約すると摩耗はこれらの効果によつて極端に低下さ
せられそして摩擦のパートナー及び潤滑剤の耐用年数は
はつきりと延長される。本発明によつてこれらの改善は
今まで高粘度又は中間の粘度を有する油の使用が絶対必
要であると考えられてきた、たとえば歯車、差動歯車、
又はタービンの歯車の分野に今や低粘度を有する油が使
用することができるように非常に広い粘度範囲に成し遂
げられる。その上本発明の潤滑剤及び潤滑剤濃縮物の熱
安定性は、ジーゼルエンジン及び航空機のタービンのよ
うな高い運転温度にさらされる潤滑場所に使用すること
を可能にする。
In summary, wear is greatly reduced by these effects and the service life of friction partners and lubricants is prolonged. According to the invention, these improvements have heretofore been considered to require the use of oils of high or medium viscosity, such as gears, differential gears,
Alternatively, a very wide viscosity range is achieved so that oils with low viscosity can now be used in the field of turbine gears. Moreover, the thermal stability of the lubricants and lubricant concentrates of the present invention allow for use in lubricated locations exposed to high operating temperatures, such as diesel engines and aircraft turbines.

本発明の好ましい実施態様に従つて潤滑剤又は潤滑剤
濃縮物は化合物(b)として、その水酸基が6〜18個の
炭素原子、好ましくは6〜12個の炭素原子、特に8〜12
個の炭素原子を有する直鎖又は有枝アルキル、アラルキ
ル又はアリール基によつてエーテル化又はエトキシエー
テル化されるモノ−、ジ−又はトリペンタエリスリトー
ルを含有する。
According to a preferred embodiment of the present invention, the lubricant or lubricant concentrate comprises as compound (b) the hydroxyl group of 6 to 18 carbon atoms, preferably 6 to 12 carbon atoms, especially 8 to 12 carbon atoms.
It contains mono-, di- or tripentaerythritol which is etherified or ethoxyetherified by a straight-chain or branched alkyl, aralkyl or aryl group having three carbon atoms.

本発明のさらに好ましい実施態様に従つて成分(b)
としてペンタエリスリトールのモノ−、ジ−又はテトラ
エーテルを含有する。
Component (b) according to a further preferred embodiment of the present invention
As pentaerythritol mono-, di- or tetraethers.

本発明の好ましい実施態様に従つて本発明の潤滑剤又
は潤滑剤濃縮物はその上に少なくとも1個の遊離水酸基
を有する化合物を含有する。
According to a preferred embodiment of the present invention, the lubricant or lubricant concentrate of the present invention contains a compound having at least one free hydroxyl group thereon.

本発明の好ましい実施態様に従つて潤滑剤又は潤滑剤
濃縮物は鉱油及び/又は合成油の重量を基準にして0.1
〜40重量%、好ましくは0.1〜20重量%、特に1〜12重
量%、特別に2〜6重量%の成分(b)を含有する。
According to a preferred embodiment of the present invention, the lubricant or lubricant concentrate is 0.1% by weight of mineral oil and / or synthetic oil.
It contains up to 40% by weight, preferably 0.1 to 20% by weight, in particular 1 to 12% by weight, in particular 2 to 6% by weight, of component (b).

本発明のさらにまた好ましい実施態様に従つて、本発
明の潤滑剤又は潤滑剤濃縮物は成分(b)としてモノ
−、ジ−又はトリペンタエリスリトールのエーテル誘導
体及び/又はエトキシル化エーテル誘導体及び/又はテ
ロメル酸ペンタエリスリトールエーテル又はそのエトキ
シル誘導体を含有する。
According to a still further preferred embodiment of the invention, the lubricants or lubricant concentrates according to the invention comprise, as component (b), mono-, di- or tripentaerythritol ether derivatives and / or ethoxylated ether derivatives and / or Contains pentaerythritol telomerate or an ethoxyl derivative thereof.

本発明の潤滑剤又は潤滑剤濃縮物は20℃で1.0mPa.s〜
20℃で2・106mPa.sの範囲の粘度を有する好ましくはビ
ート油、天然油及び/又は合成油を基油として含有す
る。特に好ましくは天然油として20℃で1.0mPa.s〜50℃
で540mPa.sの粘度を有する鉱油の使用、及び芳香族又は
脂肪族ジカルボン酸、特にポリ−α−オレフイン−ジカ
ルボン酸エステル、特別に1000〜3000の範囲内の分子量
を有する−ブチルエステルの使用、好ましくはフタル酸
ジイソデシルエステル、トリメチルアジピン酸ジデシル
エステル及びセバシン酸ジオクチルエステル、1000〜10
0000の分子量及び100℃で200〜43000mPa.sの粘度を有す
るポリイソブチレン、100℃で1000mPa.sの粘度を有する
ポリメタクリレート、100℃で5〜60mPa.sの粘度を有す
る水に不溶性のポリグリコール、50℃より高い引火点と
20℃で1.0mPa.s〜20℃で2000000mpa.sの範囲の粘度を有
するイソパラフイン油及び/又はアルキルベンゼン、及
びテロメル酸エステル、好ましくはネオペンチルグリコ
ール及び/又はテロメル酸のトリメチロールプロパンエ
ステルの使用である。
The lubricant or lubricant concentrate of the present invention is 1.0 mPa.s at 20 ° C.
It preferably contains beet oil, natural oil and / or synthetic oil having a viscosity in the range of 2 · 10 6 mPa · s at 20 ° C. as base oil. Particularly preferably, as a natural oil, 1.0 mPa.s to 50 ° C at 20 ° C.
Use of mineral oils having a viscosity of 540 mPa.s, and of aromatic or aliphatic dicarboxylic acids, in particular poly-α-olefin-dicarboxylic esters, especially -butyl esters having a molecular weight in the range from 1000 to 3000, Preferably diisodecyl phthalate, didecyl trimethyladipate and dioctyl sebacate, 1000 to 10
Polyisobutylene having a molecular weight of 0000 and a viscosity of 200-43000 mPa.s at 100 ° C., polymethacrylate having a viscosity of 1000 mPa.s at 100 ° C., and a water-insoluble polyglycol having a viscosity of 5-60 mPa.s at 100 ° C. With flash point higher than 50 ℃
Use of isoparaffin oil and / or alkylbenzene having a viscosity in the range of 1.0 mPa.s at 20 DEG C. to 2,000,000 mpa.s at 20 DEG C., and telomerates, preferably trimethylolpropane ester of neopentyl glycol and / or telomerate. It is.

更なる添加剤として本発明の潤滑剤又は潤滑剤濃縮物
は好ましくは硫黄含有物質、特にチアゾール、少なくと
も1個の金属ジアルキルジチオカルバメート及び/又は
金属ジアルキルジチオフオスフアート及び/又はリン含
有物質、特に有機ホスフアイト、好ましくはジアルキル
アリールホスフアイト、特別にジデシルフエニルホスフ
アイト又はジドデシルフエニルホスフアイト及び/又は
金属ジアルキルジチオフオスフアートを含有する。
As further additives, the lubricants or lubricant concentrates according to the invention are preferably sulfur-containing substances, especially thiazoles, at least one metal dialkyldithiocarbamate and / or metal dialkyldithiophenophthalate and / or phosphorus-containing substances, in particular It contains an organic phosphite, preferably a dialkylaryl phosphite, especially didecylphenyl phosphite or didodecylphenyl phosphite and / or a metal dialkyldithiophenophosphate.

硫黄含有物質は好ましくは本発明の潤滑剤又は潤滑剤
濃縮物中に0.5〜10重量%、特に1〜3重量%の量で含
有され、その上リン含有物質を好ましくは0.1〜10重量
%、特に0.1〜5重量%、特別に0.5〜2重量%の量で含
有する。
The sulfur-containing material is preferably contained in the lubricant or lubricant concentrate according to the invention in an amount of 0.5 to 10% by weight, in particular 1 to 3% by weight, while the phosphorus-containing material is preferably 0.1 to 10% by weight, In particular, it is contained in an amount of 0.1 to 5% by weight, especially 0.5 to 2% by weight.

本発明のさらに好ましい実施態様に従つて潤滑剤又は
潤滑剤濃縮物は通常の酸化防止剤、金属失活剤、洗浄
剤、分散剤、消泡剤及び/又は粘度指数改善剤を含有す
ることができる。
According to a further preferred embodiment of the present invention, the lubricant or lubricant concentrate may contain conventional antioxidants, metal deactivators, detergents, dispersants, defoamers and / or viscosity index improvers. it can.

本発明の添加剤は単一化合物として又は基礎媒質(基
油又は基礎脂肪)に対して濃縮物として組成物の形で上
述の量を添加することが可能である。
The additives according to the invention can be added in the abovementioned amounts in the form of a composition as a single compound or as a concentrate with respect to the base medium (base oil or base fat).

本発明の更なる特長及び利点は本発明の以下の記述か
らわかるであろう。
Further features and advantages of the invention will be apparent from the following description of the invention.

分子中に少なくとも1個の第4級炭素原子を有し本発
明によつて好ましく使用されるポリエーテル化合物は以
下の群の化合物を含むことができる。
The polyether compounds having at least one quaternary carbon atom in the molecule and preferably used according to the invention can include the following groups of compounds:

a) モノ−、ジ−及びトリペンタエリスリトールエー
テル及びそれらのエトキシル化エーテル誘導体。基本的
モノ−及びジペンタエリスリトールは以下の構造を有
し、 ただし水酸基は部分的に又は完全にエーテル化され、そ
してそのエーテル基は6〜18個、好ましくは8〜12個の
炭素原子を有する直鎖又は分枝アルキル、アラルキル又
はアリール基を含有することが好ましい。
a) Mono-, di- and tripentaerythritol ethers and their ethoxylated ether derivatives. Basic mono- and dipentaerythritol have the following structure: However, the hydroxyl groups can be partially or completely etherified, and the ether groups can contain straight-chain or branched alkyl, aralkyl or aryl groups having 6 to 18, preferably 8 to 12, carbon atoms. preferable.

これらの化合物は容易に調製できまたこれらの化合物
のたくさんの代表者は商業的に入手することができる。
These compounds can be easily prepared and many representatives of these compounds are commercially available.

適切なペンタエリスリトールエーテルの例はペンタエ
リスリトール モノヘキシルエーテル、ペンタエリスリ
トール モノオクチルエーテル、ペンタエリスリトール
モノノニルエーテル、ペンタエリスリトール モノデシ
ルエーテル、ペンタエリスリトール モノドデシルエー
テル、ペンタエリスリトール モノミリスチルエーテ
ル、ペンタエリスリトール モノヘキサデシルエーテ
ル、ペンタエリスリトール モノステアリルエーテル、
ペンタエリスリトール モノオレイルエーテル、ペンタ
エリスリトール モノイソステアリル−及び−イソパル
ミチン酸エーテル;ペンタエリスリトールの相当するジ
ヘキシル−、ジオクチル−、ジノニル−、ジデシル−、
ジドデシル−、ジミリスチル−、ジヘキサデシル−、ジ
ステアリル−、ジオレイル−、ジイソステアリル−及び
ジイソパルミチン酸エーテル;ペンタエリスリトールの
相当するトリヘキシル−、トリオクチル−、トリノニル
−、トリデシル−、トリドデシル−、トリミリスチル
−、トリヘキサデシル−、トリステアリル−、トリオレ
イル−、トリイソステアリル−及びトリイソパルミチン
酸エーテルだけでなくペンタエリスリトールの相当する
テトラヘキシル−、テトラオクチル−、テトラノニル
−、テトラデシル−、テトラドデシル−、テトラミリス
チル−、テトラヘキサデシル−、テトラステアリル−、
テトラオレイル−、テトライソステアリル−及びテトラ
イソパルミチン酸エーテルである。
Examples of suitable pentaerythritol ethers are pentaerythritol monohexyl ether, pentaerythritol monooctyl ether, pentaerythritol monononyl ether, pentaerythritol monodecyl ether, pentaerythritol monododecyl ether, pentaerythritol monomyristyl ether, pentaerythritol monohexadecyl ether , Pentaerythritol monostearyl ether,
Pentaerythritol monooleyl ether, pentaerythritol monoisostearyl- and -isopalmitate ethers; the corresponding dihexyl-, dioctyl-, dinonyl-, didecyl- of pentaerythritol
Didodecyl-, dimyristyl-, dihexadecyl-, distearyl-, dioleyl-, diisostearyl- and diisopalmitate ethers; the corresponding trihexyl-, trioctyl-, trinonyl-, tridecyl-, tridodecyl-, trimyristyl- of pentaerythritol , Trihexadecyl-, tristearyl-, trioleyl-, triisostearyl- and triisopalmitate ethers as well as the corresponding tetrahexyl-, tetraoctyl-, tetranonyl-, tetradecyl-, tetradodecyl-, of pentaerythritol Tetramyristyl-, tetrahexadecyl-, tetrastearyl-,
Tetraoleyl-, tetraisostearyl- and tetraisopalmitate ethers.

b) 次の骨格を持つペンタエリスリトールテロメル酸
誘導体: 式中Tはテロマーであり RはT又はアルキルである。
b) Pentaerythritol telomeric acid derivative having the following skeleton: Wherein T is a telomer and R is T or alkyl.

テロメル酸は比較的高い分子量を有して長鎖星状分子
構造を有する化合物であり、それは通例の方法でエーテ
ル化することができてそのエーテルは価値のある潤滑剤
である(アクゾ ケミストリー社の市販製品Kortacid
T)。
Telomeric acid is a compound having a relatively high molecular weight and a long chain star molecular structure, which can be etherified in a customary manner, and the ether is a valuable lubricant (Akzo Chemistry) Commercial product Kortacid
T).

本発明によつて使用することができる鉱油は、20℃で
1.0mPa.sの粘度を有するイソパラフイン油から20℃で12
mPa.sの粘度を有する薄いスピンドル油を越えて高粘稠
なブライトストツク(brightstock)及び50℃で540mPa.
sの粘度を有するシリンダー油に至るすべての通例の鉱
油である。
The mineral oil which can be used according to the invention is at 20 ° C.
From isoparaffin oil having a viscosity of 1.0 mPa.s
Beyond thin spindle oil with a viscosity of mPa.s, a highly viscous brightstock and 540 mPa.s at 50 ° C.
All customary mineral oils up to cylinder oils with a viscosity of s.

本発明によつて使用できる合成油の多くは、たとえば
BP社から商号“Hyvis 10"(100℃で200mPa.sの粘度を有
するポリイソブチレン)、“Hyvis 200"(100℃で4300m
Pa.sの粘度を有するポリイソブチレン)及び“Hyvis 20
00"(100℃で43000mPa.sの粘度を有するポリイソブチレ
ン)のもとで商業的に入手できる。100℃で1000mPa.sの
粘度を有するレーム(Rhm)社のViscoplex 4−95
(ポリメタクリレート)、ユニオンカーバイド社の100
℃で5.7mPa.sの粘度を有するUcolub N9、100℃で5.7mP
a.sの粘度を有するUcolub N36A、100℃で55mPa.sの粘
度を有するUcolub N36A、100℃で55mpa.sの粘度をUcol
ub N120A(これらのすべては水に不溶性のポリグリコ
ールである)だけでなく20℃で1.0mPa.sの粘度を有する
エツソ社の“Isopar J"(イソパラフイン油)も商業的
に入手可能である。
Many of the synthetic oils that can be used according to the invention include, for example,
BP's trade name “Hyvis 10” (polyisobutylene having a viscosity of 200 mPa.s at 100 ° C.), “Hyvis 200” (4300 m at 100 ° C.)
Polyisobutylene having a viscosity of Pa.s) and "Hyvis 20
Commercially available under "00" (polyisobutylene having a viscosity of 43000 mPa.s at 100 DEG C.) Viscoplex 4-95 from Rhhm having a viscosity of 1000 mPa.s at 100 DEG C.
(Polymethacrylate), Union Carbide 100
Ucolub N9 with a viscosity of 5.7 mPa.s at ℃, 5.7 mP at 100 ℃
Ucolub N36A with viscosity of as, Ucolub N36A with viscosity of 55 mPa.s at 100 ° C, Ucol with viscosity of 55 mpa.s at 100 ° C
Not only ub N120A (all of which are water-insoluble polyglycols) but also Etsuso's "Isopar J" (isoparaffin oil) having a viscosity of 1.0 mPa.s at 20 ° C. is commercially available. .

本発明に従つて使用できるリン含有化合物は下式の有
機リン化合物であり 式中Rはそれぞれ6〜12個の炭素原子を有する直鎖又は
有枝又は環式アルキル基、又は1〜6個の炭素原子を有
する低級アルキル基によつてO−又はP−位置で置換さ
れたフエニル基である。
The phosphorus-containing compound which can be used according to the invention is an organic phosphorus compound of the formula Wherein R is substituted at the O- or P-position by a straight-chain or branched or cyclic alkyl group, each having 6 to 12 carbon atoms, or a lower alkyl group having 1 to 6 carbon atoms. Phenyl group.

上記の式を有する有機化合物の好ましい例はモノデシ
ル−ジフエニルホスフアイト、ジデシルフエニルホスフ
アイト、トリフエニルホスフアイト、ジオクチル−フエ
ニルホスフアイト、ジヘキシル−フエニル−ホスフアイ
ト、ジイソデシル−フエニル−ホスフアイト、ジイソオ
クチル−フエニル−ホスフアイト、ジデシル−O−メチ
ル−フエニルホスフアイト及びジデシル−P−メチルフ
エニルホスフアイトである。
Preferred examples of the organic compound having the above formula include monodecyl-diphenyl phosphite, didecyl phenyl phosphite, triphenyl phosphite, dioctyl-phenyl phosphite, dihexyl-phenyl-phosphite, diisodecyl-phenyl-phosphite, and diisooctyl. Phenyl-phosphite, didecyl-O-methyl-phenylphosphite and didecyl-P-methylphenylphosphite.

硫黄含有物質として本発明に使用できる金属ジアルキ
ルジチオカルバメートは下式の化合物であり 式中Meは銅(Cu)、銀(Ag)、亜鉛(Zn)、カドミウム
(Cd)、チタン(Ti)、ホウ素(B)、ジルコン(Z
r)、スズ(Sn)、鉛(Pb)、バナジウム(V)、タン
タル(Ta)、アンチモン(Sb)、クロム(Cr)、モリブ
デン(Mo)、タングステン(W)、マンガン(Mn)、コ
バルト(Co)、及びニツケル(Ni)からなる群から選ば
れた金属であり、好ましくはホウ素(B)、ニツケル
(Ni)、コバルト(Co)又はモリブデン(Mo)である。
The metal dialkyldithiocarbamate that can be used in the present invention as a sulfur-containing substance is a compound of the following formula: In the formula, Me is copper (Cu), silver (Ag), zinc (Zn), cadmium (Cd), titanium (Ti), boron (B), zircon (Z
r), tin (Sn), lead (Pb), vanadium (V), tantalum (Ta), antimony (Sb), chromium (Cr), molybdenum (Mo), tungsten (W), manganese (Mn), cobalt ( Co) and a metal selected from the group consisting of nickel (Ni), preferably boron (B), nickel (Ni), cobalt (Co) or molybdenum (Mo).

リン含有物質のみならず硫黄含有物質として本発明に
使用できる金属ジアルキルジチオホスフアートは下式の
化合物であり 式中Meは銅(Cu)、銀(Ag)、亜鉛(Zn)、カドミウム
(Cd)、チタン(Ti)、ホウ素(B)、ジルコン(Z
r)、スズ(Sn)、鉛(Pb)、バナジウム(V)、タン
タル(Ta)、アンチモン(Sb)、クロム(Cr)、モリブ
デン(Mo)、タングステン(W)、マンガン(Mn)、コ
バルト(Co)、及びニツケル(Ni)からなる群から選ば
れた金属であり、好ましくは亜鉛(Zn)、ニツケル(N
i)、チタン(Ti)、バナジウム(V)、モリブデン(M
o)、タングステン(W)及びマンガン(Mn)である。
The metal dialkyldithiophosphate usable in the present invention as a sulfur-containing substance as well as a phosphorus-containing substance is a compound of the following formula: In the formula, Me is copper (Cu), silver (Ag), zinc (Zn), cadmium (Cd), titanium (Ti), boron (B), zircon (Z
r), tin (Sn), lead (Pb), vanadium (V), tantalum (Ta), antimony (Sb), chromium (Cr), molybdenum (Mo), tungsten (W), manganese (Mn), cobalt ( Co) and nickel (Ni), preferably zinc (Zn), nickel (N
i), titanium (Ti), vanadium (V), molybdenum (M
o), tungsten (W) and manganese (Mn).

上述の金属ジアルキルジチオカルバメート及び金属ジ
アルキルジチオホスファートのアルキル基はそれぞれ好
ましくは4〜8個の炭素原子を有しているため、選択さ
れる金属塩は市販の基油に溶解する。特に都合のよいア
ルキル基の例はn−、i−及びtert−ブチル基、n−及
びi−アミル基、n−及びi−ヘキシル基、n−及びi
−ヘプチル基及び2−エチルヘキシル基である。特別に
好ましいものはi−ブチル基、n−及びi−アミル基及
び2−エチルヘキシル基である。
Since the alkyl groups of the above-mentioned metal dialkyldithiocarbamates and metal dialkyldithiophosphates each preferably have 4 to 8 carbon atoms, the metal salt selected dissolves in a commercially available base oil. Examples of particularly convenient alkyl groups are n-, i- and tert-butyl, n- and i-amyl, n- and i-hexyl, n- and i.
-Heptyl group and 2-ethylhexyl group. Particularly preferred are i-butyl, n- and i-amyl and 2-ethylhexyl.

本発明によつて有利に使用することができる金属ジア
ルキルジチオカルバメートの例は以下のものである:銅
−ジアルキルジチオカルバメート及び銅−ビス−ジアル
キルジチオカルバメート、銀−ジアルキルジチオカルバ
メート、亜鉛−及びカドミウム−ビス−ジアルキルジチ
オカルバメート、ホウ素−トリスジアルキルジチオカル
バメート、同様にスズ−及び鉛−ビス−ジアルキルジチ
オカルバメート、アンチモン−、バナジウム−、タンタ
ル−トリス−ジアルキルジチオカルバメート、−テトラ
キス−、及び−ペンタキスジアルキルジチオカルバメー
ト、同様にその中のこれらの金属が混合した酸化度で存
在するジアルキルジチオカルバメート;クロム−ビス
−、クロム−トリス、クロム−テトラキス、及びクロム
−ヘキサキスジアルキルチオカルバメート、モリブデン
−、及びタングステン−テトラキス−、−ヘキサキス
−、及び−オキシビス−及び−オキシテトラキスジアル
キルジチオカルバメート、マンガン−ビス−、−トリス
−、−テトラキス−及び−ヘキサキスジアルキルジチオ
カルバメート、及びコバルト−及びニッケル−ビス−及
び−トリスジアルキルジチオカルバメート。
Examples of metal dialkyldithiocarbamates which can be advantageously used according to the invention are: copper-dialkyldithiocarbamate and copper-bis-dialkyldithiocarbamate, silver-dialkyldithiocarbamate, zinc- and cadmium-. Bis-dialkyldithiocarbamates, boron-trisdialkyldithiocarbamates, as well as tin- and lead-bis-dialkyldithiocarbamates, antimony-, vanadium-, tantalum-tris-dialkyldithiocarbamates, -tetrakis-, and -pentakisdialkyldithios Carbamates, also dialkyldithiocarbamates in which these metals are present in mixed degrees of oxidation; chromium-bis-, chromium-tris, chromium-tetrakis, and chromium-hexakisdialkyl Thiocarbamates, molybdenum- and tungsten-tetrakis-, -hexakis-, and -oxybis- and -oxytetrakisdialkyldithiocarbamates, manganese-bis-, -tris-, -tetrakis- and -hexakisdialkyldithiocarbamates, and cobalt -And nickel-bis- and -trisdialkyldithiocarbamates.

これらの化合物の中でホウ素−トリスジアルキルジチ
オカルバメート、ニツケル−トリスジアルキルジチオカ
ルバメート、モリブデン−テトラキス−及びモリブデン
−オキシテトラキスジアルキルジチオカルバメート、マ
ンガン−、バナジウム−、及びタングステン−テトラキ
スジアルキルジチオカルバメートが特に好ましい。
Among these compounds, boron-trisdialkyldithiocarbamate, nickel-trisdialkyldithiocarbamate, molybdenum-tetrakis- and molybdenum-oxytetrakisdialkyldithiocarbamate, manganese-, vanadium- and tungsten-tetrakisdialkyldithiocarbamate are particularly preferred.

本発明によつて有利に使用することができる金属ジア
ルキルホスフアートは金属ジアルキルジチオカルバメー
トに対して上記に一覧表にしたように同じ酸化度の同じ
金属のジアルキルジチオホスフアートである。
The metal dialkyl phosphates which can be advantageously used according to the invention are the same metal dialkyl dithio phosphates of the same degree of oxidation as listed above for the metal dialkyl dithiocarbamates.

特に都合よいものは亜鉛−ビスジアルキルジチオホス
フアート、ニツケル−ビス−及び−トリスジアルキルジ
チオホスフアート、チタン−及びバナジウム−テトラキ
スジアルキルジチオホスフアート、モリブデン−及びタ
ングステン−テトラキスアルキルジチオホスフアート及
びモリブデン−及びタングステン−オキシテトラキスジ
アルキルジチオホスフアートである。
Particularly advantageous are zinc-bisdialkyldithiophosphato, nickel-bis- and -trisdialkyldithiophosphato, titanium- and vanadium-tetrakisdialkyldithiophosphato, molybdenum- and tungsten-tetrakisalkyldithiophosphato and molybdenum- and Tungsten-oxytetrakisdialkyldithiophosphate.

本発明によつて使用される金属ジアルキルジチオカル
バメートの特に好ましい見本は、ホウ素−トリスジイソ
ブチルジチオカルバメート、ホウ素−トリスジ−2−エ
チルヘキシルジチオカルバメート、ニツケル−トリスジ
イソブチルジチオカルバメート、ニツケル−トリスジア
ミルジチオカルバメート、ニツケル−トリスジ−2−エ
チルヘキシルジチオカルバメート、モリブデン−テトラ
キスジ−2−エチルヘキシルジチオカルバメート、モリ
ブデン−オキシテトラキスジ−2−エチルヘキシルジチ
オカルバメート、マンガン−、バナジウム−及びタング
ステン−テトラキス−2−エチルヘキシルジチオカルバ
メート、同様にコバルト−ビス−ジイソブチルジチオカ
ルバメートである。
Particularly preferred samples of the metal dialkyldithiocarbamates used according to the invention are boron-trisdiisobutyldithiocarbamate, boron-trisdi-2-ethylhexyldithiocarbamate, nickel-trisdiisobutyldithiocarbamate, nickel-trisdiamildithiocarbamate, Nickel-trisdi-2-ethylhexyldithiocarbamate, molybdenum-tetrakisdi-2-ethylhexyldithiocarbamate, molybdenum-oxytetrakisdi-2-ethylhexyldithiocarbamate, manganese-, vanadium- and tungsten-tetrakis-2-ethylhexyldithiocarbamate, likewise Cobalt-bis-diisobutyldithiocarbamate.

本発明によつて使用される金属ジアルキルジチオホス
フエートの特に好ましい見本は亜鉛−ビス−ジ−2−エ
チルヘキシルジチオホスフアート、ニツケル−ビス−及
び−トリスジ−2−エチルヘキシルジチオホスフアー
ト、マンガン−、チタン−及びバナジウム−テトラキス
ジ−2−エチルヘキシルジチオホスフアート、同様にモ
リブデン−及びタングステン−テトラキス−及びモリブ
デン−及びタングステン−オキシテトラキスジ−2−エ
チルヘキシルジチオホスフアートである。
Particularly preferred examples of the metal dialkyldithiophosphates used according to the invention are zinc-bis-di-2-ethylhexyldithiophosphate, nickel-bis- and -trisdi-2-ethylhexyldithiophosphate, manganese, titanium. -And vanadium-tetrakisdi-2-ethylhexyldithiophosphato, as well as molybdenum- and tungsten-tetrakis- and molybdenum- and tungsten-oxytetrakisdi-2-ethylhexyldithiophosphato.

本発明は以下の実施例を使用してより詳細に説明され
るが、これに限定されものではない。
The present invention will be described in more detail using the following examples, but is not limited thereto.

以下の実施例において市販の潤滑油及び潤滑脂肪は、
それぞれ以下の組成を持つものが使用され、そしてそれ
らは一方において本発明の潤滑剤濃縮物を含有するもの
他方においてそれを含有しないものであるが、それらの
潤滑性に関して比較された。
In the following examples, commercially available lubricating oils and fats are:
Each of the following compositions was used, and they were compared with respect to their lubricity, on the one hand containing the lubricant concentrate of the invention and on the other hand not containing it.

各実施例において得た結果は図にグラフ状に描写す
る。
The results obtained in each example are depicted graphically in the figures.

試験を実行するために直径23mm厚さ10mmの精製された
鋼製の円板が使用され、その表面に試験されるべき各潤
滑剤又は潤滑剤濃縮物の一滴を塗布した。潤滑剤又は潤
滑剤濃縮物の滴が置かれた領域の上に、金属板の表面上
にその荷重が圧力を及ぼすために、直径10mmの同じ精製
された鋼製の球を置いた。金属球は圧力下に60〜180分
間1mmの振幅にわたつて50Hzの頻度で金属板の表面を動
きそして逆もどりした。試験の間じゆう負荷領域内の荷
重は50〜300Nに変動し、温度は50〜150℃に変化した(O
ptimol GmbH商会によつて世界的に販売されているSRV
(振動−摩擦−摩耗)装置)。
A refined steel disc 23 mm in diameter and 10 mm thick was used to perform the test, and the surface was coated with a drop of each lubricant or lubricant concentrate to be tested. Above the area where the lubricant or lubricant concentrate drops were placed, the same refined steel sphere of 10 mm diameter was placed so that the load exerted pressure on the surface of the metal plate. The metal sphere moved under the pressure on the surface of the metal plate at a frequency of 50 Hz over an amplitude of 1 mm for 60-180 minutes and back again. The load in the load area during the test varied from 50 to 300N and the temperature changed from 50 to 150 ° C (O
SRV sold worldwide by ptimol GmbH Shokai
(Vibration-friction-wear) device).

球の発振方向に対角線の試験期間内の金属板の表面と
負荷する球の間の摩擦のために生じた摩耗痕(摩耗によ
り生じた凹凸の輪郭)は適切な記録装置によつて記録し
た。下記に示す図が得られ、縦軸に、摩耗の高さは金属
板の表面の摩耗痕の最高点と最低点との間の差として、
さらにまた横軸上に金属板の表面の走査範囲を描く。
Abrasion marks caused by friction between the surface of the metal plate and the loaded sphere during a test period diagonally to the oscillating direction of the sphere (contour of unevenness caused by abrasion) were recorded by an appropriate recording device. The figure shown below is obtained, on the vertical axis, the height of wear is the difference between the highest and lowest points of wear marks on the surface of the metal plate,
Furthermore, the scanning range of the surface of the metal plate is drawn on the horizontal axis.

以下の図において縦軸の摩耗痕の1cmの深さは金属板
の表面の摩耗痕の1μmの本当の深さに相当する。だが
一方実施例2の図B′においては走査装置は図の摩耗痕
の1cmの深さが板の表面の摩耗痕の2.5μmの本当の深さ
に相当するように弱められた。
In the following figures, a depth of 1 cm of the wear mark on the vertical axis corresponds to a true depth of 1 μm of the wear mark on the surface of the metal plate. However, in FIG. B 'of Example 2, the scanning device was weakened so that the 1 cm depth of the wear marks in the figure corresponded to the true depth of 2.5 μm of the wear marks on the plate surface.

図は同一条件のもとに記録された(球の荷重50〜300
N、摩擦頻度50Hz、温度50〜150℃、摩擦振幅1mm、試験
時間1〜3時間)。
The figures were recorded under the same conditions (ball load 50-300
N, friction frequency 50 Hz, temperature 50 to 150 ° C., friction amplitude 1 mm, test time 1 to 3 hours).

以下の図に示した摩擦係数(RKmax=最大摩擦係数;RK
d=摩擦係数曲線の98%にわたる平均摩擦係数)は上記
のSRV装置を使用して測定した。別のやり方で述べない
かぎりすべての試験において、本発明の潤滑剤濃縮物と
して以下の組成を有する製品を使用した: 実施例1 50℃で2200mPa.sの粘度を有し、下記の組成を有する
高粘稠潤滑油を調製し試験した: トリメチルアジピン酸ジデシルエステル 34% ポリイソブチレン(43000mpa.s/100℃) 32% 潤滑剤混入物質 6% 本発明の潤滑剤濃縮物 28% 比較製品においては本発明の潤滑剤濃縮物は除外し
た。
The coefficient of friction shown in the following figure (R K max = maximum coefficient of friction; R K
d = mean coefficient of friction over 98% of the coefficient of friction curve) was measured using the SRV apparatus described above. Unless stated otherwise, in all tests, products having the following composition were used as lubricant concentrates according to the invention: Example 1 A highly viscous lubricating oil having a viscosity of 2200 mPa.s at 50 ° C. and having the following composition was prepared and tested: trimethyl adipate didecyl ester 34% polyisobutylene (43000 mpa.s / 100 ° C.) 32 % Lubricant contaminants 6% Inventive lubricant concentrate 28% In comparative products, inventive lubricant concentrate was excluded.

両製品は同一条件のもとで温度150℃、荷重200Nで1
時間試験した。得られた結果を下記の図A(本発明によ
る)及びA′(現在の技術水準による)にグラフ状に描
く。
Both products are 1 under the same conditions at a temperature of 150 ° C and a load of 200N.
Time tested. The results obtained are plotted graphically in the following figures A (according to the invention) and A '(according to the state of the art).

本発明の潤滑剤濃縮物の添加は1.13μm(2回の測定
の平均)の摩耗痕の深さを導く。本発明の潤滑剤濃縮物
の添加なしで1.68μm(2回の測定の平均)の摩耗痕の
深さが得られた。
The addition of the lubricant concentrate according to the invention leads to a wear scar depth of 1.13 μm (average of two measurements). A wear scar depth of 1.68 μm (average of two measurements) was obtained without the addition of the lubricant concentrate of the invention.

実施例2 50℃で190〜200mPa.sの粘度を有し、下記の組成を有
する中程度の粘稠さの潤滑油を調製し試験した: 重合体のα−オレフインエステル 12% トリメチルアジピン酸ジデシルエステル 36% ポリイソブチレン(43000mpa.s/100℃) 18% 潤滑剤混入物質 6% 本発明の潤滑剤濃縮物 28% 比較製品においては本発明の潤滑剤濃縮物は除外し
た。
Example 2 A moderately viscous lubricating oil having a viscosity of 190-200 mPa.s at 50 DEG C. and having the following composition was prepared and tested: Polymer alpha-olefin ester 12% trimethyladipate Decyl ester 36% Polyisobutylene (43000 mpa.s / 100 ° C.) 18% Lubricant contaminants 6% Inventive lubricant concentrate 28% In comparative products, the inventive lubricant concentrate was excluded.

両製品は同一条件のもとで温度150℃、荷重200Nで1
時間試験した。得られた結果を下記の図B(本発明によ
る)及びB′(現在の技術水準による)にグラフ状に描
く。
Both products are 1 under the same conditions at a temperature of 150 ° C and a load of 200N.
Time tested. The results obtained are depicted graphically in the following figures B (according to the invention) and B '(according to the state of the art).

本発明の潤滑剤濃縮物の添加は0.90μm(2回の測定
の平均)の摩耗痕の深さを導いた。本発明の潤滑剤濃縮
物の添加なしで13.98μm(2回の測定の平均)の摩耗
痕の深さが得られた。
The addition of the lubricant concentrate of the invention led to a wear scar depth of 0.90 μm (average of two measurements). A wear scar depth of 13.98 μm (average of two measurements) was obtained without the addition of the lubricant concentrate of the invention.

実施例3 50℃で120〜150mPa.sの粘度を有し、下記の組成を有
する中間の粘稠さの潤滑油を調製し試験した: 高粘稠のα−オレフインエステル共重合体 4% 中間の粘稠さのα−オレフインエステル重合体 12% トリメチルアジピン酸ジデシルエステル 34% ポリイソブチレン(200mpa.s/100℃) 12% 潤滑剤混入物質 6% 本発明の潤滑剤濃縮物 32% 比較製品においては本発明の潤滑剤濃縮物は除外し
た。
Example 3 An intermediate viscous lubricating oil having a viscosity of 120-150 mPa.s at 50 DEG C. and having the following composition was prepared and tested: High viscous alpha-olefin ester copolymer 4% intermediate Α-olefin ester polymer with a consistency of 12% Didecyl trimethyl adipate 34% Polyisobutylene (200mpa.s / 100 ° C) 12% Lubricant contamination 6% Lubricant concentrate of the invention 32% Comparative product In the above, the lubricant concentrate of the present invention was excluded.

両製品は同一の条件のもとで温度150℃、荷重200Nで
1時間試験した。得られた結果を下記の図C(本発明に
よる)及びC′(現在の技術水準による)にグラフ状に
描く。
Both products were tested under the same conditions at a temperature of 150 ° C. and a load of 200 N for 1 hour. The results obtained are depicted graphically in the following figures C (according to the invention) and C '(according to the state of the art).

本発明の潤滑剤濃縮物の添加は1.03μm(2回の測定
の平均)の摩耗痕の深さを引き起こした。本発明の潤滑
剤濃縮物の添加なしで3.48μm(2回の測定の平均)の
摩耗痕の深さが得られた。
The addition of the lubricant concentrate of the present invention caused a wear scar depth of 1.03 μm (average of two measurements). A wear scar depth of 3.48 μm (average of two measurements) was obtained without the addition of the lubricant concentrate of the invention.

実施例4 50℃で15000mPa.sの粘度を有し、下記の組成を有する
高粘稠粘着性の高温潤滑油を調製して試験した: トリメチルアジピン酸ジデシルエステル 29% ポリイソブチレン(43000mpa.s/100℃) 52% 本発明の潤滑剤濃縮物 19% 比較製品においては本発明の潤滑剤濃縮物は除外し
た。
Example 4 A highly viscous, sticky, high temperature lubricating oil having a viscosity of 15000 mPa.s at 50 ° C. and the following composition was prepared and tested: trimethyladipate didecyl ester 29% polyisobutylene (43000 mpa.s) / 100 ° C.) 52% Lubricant concentrate of the invention 19% In comparative products, the lubricant concentrate of the invention was excluded.

両製品は同一条件のもとで温度150℃、荷重200Nで1
時間試験した。得られた結果は下記の図D(本発明によ
る)及びD′(現在の技術水準による)にグラフ状に描
く。
Both products are 1 under the same conditions at a temperature of 150 ° C and a load of 200N.
Time tested. The results obtained are plotted graphically in the following figures D (according to the invention) and D '(according to the state of the art).

本発明の潤滑剤濃縮物の添加は0.8μm(3回の測定
の平均)の摩耗痕の深さを引き起こした。本発明の潤滑
剤濃縮物の添加なしで1.57μm(2回の測定の平均)の
摩耗痕の深さが得られた。
Addition of the lubricant concentrate of the present invention caused a wear scar depth of 0.8 μm (average of three measurements). A wear scar depth of 1.57 μm (average of two measurements) was obtained without the addition of the lubricant concentrate of the invention.

実施例5 下記の組成を有する高機械効率の歯車及び同調継手用
の多目的潤滑剤用潤滑脂肪が調製されて試験された: 鉱油 70% ステアリン酸リチウムに基礎を置くコンシステンシー改
良剤 9% 本発明の潤滑剤濃縮物 21% 比較製品においては本発明の潤滑剤濃縮物は3重量%
の二硫化モリブデン/黒鉛混合物で置換された。
Example 5 A lubricating fat for multipurpose lubricants for high mechanical efficiency gears and tuning joints having the following composition was prepared and tested: Mineral oil 70% Lithium stearate based consistency improver 9% The present invention Lubricant concentrate of 21% In the comparative product, the lubricant concentrate of the present invention is 3% by weight
Molybdenum disulfide / graphite mixture.

両製品は同一条件のもので温度50℃、荷重300Nで3時
間試験した。得られた結果は下記の図(本発明による)
及びF′(現在の技術水準による)にグラフ状に描く。
Both products were tested under the same conditions at a temperature of 50 ° C. and a load of 300 N for 3 hours. The results obtained are shown in the following figure (according to the invention)
And F '(according to the state of the art) in graphical form.

本発明の潤滑剤濃縮物の添加は0.95μm(3回の測定
の平均)の摩耗痕の深さを引き起こすが、一方比較添加
剤混合物の添加は1.63μm(3回の測定の平均)の摩耗
痕の深さを引き起こす。
The addition of the lubricant concentrate according to the invention causes a wear scar depth of 0.95 μm (mean of three measurements), while the addition of the comparative additive mixture results in a wear of 1.63 μm (mean of three measurements). Causes the depth of the scar.

本発明は好ましい実施態様を参照して詳細に説明され
たが、しかしながらそれに限定されるものでなくて、本
発明の範囲を越えることなく、専門家にとつて明白な方
法で多くの点で改変し修整できることは明らかである。
Although the present invention has been described in detail with reference to preferred embodiments, it is not limited thereto, but may be modified in many ways in a manner apparent to the expert without exceeding the scope of the invention. Obviously, it can be modified.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI C10M 135:18 C10M 135:18 107:08 107:08 107:22 107:22 105:36) 105:36) C10N 20:00 C10N 20:00 C Z 30:06 30:06 30:08 30:08 30:12 30:12 40:00 40:00 40:04 40:04 40:12 40:12 (56)参考文献 特開 昭58−117287(JP,A) 特開 昭59−75995(JP,A) 特開 昭58−61189(JP,A) (58)調査した分野(Int.Cl.7,DB名) C10M 169/04 C10M 129/16 C10M 129/74 C10M 137/02 C10M 137/10 C10M 135/18 C10M 107/08 C10M 107/22 C10M 105/36 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification code FI C10M 135: 18 C10M 135: 18 107: 08 107: 08 107: 22 107: 22 105: 36) 105: 36) C10N 20:00 C10N 20:00 CZ 30:06 30:06 30:08 30:08 30:12 30:12 40:00 40:00 40:04 40:04 40:12 40:12 (56) References 58-117287 (JP, A) JP-A-59-75995 (JP, A) JP-A-58-61189 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C10M 169/04 C10M 129/16 C10M 129/74 C10M 137/02 C10M 137/10 C10M 135/18 C10M 107/08 C10M 107/22 C10M 105/36

Claims (11)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】(a)天然油、合成油及びその混合物から
なる群から選ばれた基油、 (b)少なくとも0.900の密度d20を有し、且つその分子
中に少なくとも1個の第4級炭素原子を含む少なくとも
1種類の4価〜8価のアルコール誘導体であって、該ア
ルコールはモノ−、ジ−及びトリペンタエリスリトール
からなる群から選ばれ、アルコール性の基が6〜18の炭
素原子を有する直鎖若しくは有枝アルキル、アラルキル
又はアリール基を含むアルキル又はアリールハライドに
よって全てエーテル化される、少なくとも1種類の4価
〜8価のアルコール誘導体、 (c)立体障害フェノール、 (d)下記の式で表わされる少なくとも1種類のジアル
キルジチオカルバメート化合物、 (式中、Meはホウ素、バナジウム、クロム、モリブテ
ン、タングステン、マンガン、コバルト、ニッケル及び
その混合物からなる群から選ばれた金属であり、Rはそ
れぞれ独立して4〜8個の炭素原子を有するアルキル基
である。) (e)ジアルキルアリールホスファイト、モノアルキル
ジアリールホスファイト、トリアルキルホスファイト及
びトリアリールホスファイトからなる群から選ばれた少
なくとも1種類の化合物(但し、アルキル基は直鎖、有
枝又は環式であり、そして8〜12個の炭素原子を含有
し、また、アリール基は1〜6個の炭素原子を有するア
ルキル基によってo−位又はp−位が置換されたフェニ
ル基である)、 (f)チアゾール誘導体、 (g)下記の式で表わされる少なくとも1種類のジアル
キルジチオホスファート化合物、及び (式中、Meは亜鉛、モリブテン及びその混合物からなる
群から選ばれた金属であり、Rは4〜8個の炭素原子を
有するアルキル基である。) (h)酸化防止剤、金属不活性剤、洗浄剤、分散剤、消
泡剤及び粘度指数向上剤から選ばれ、前記成分(a)〜
(g)のいずれとも異なる添加剤を含有する潤滑剤であ
って、 上記成分(b)を成分(a)の重量を基準にして0.1〜4
0重量%、成分(d)と成分(g)とを合計量で0.5〜10
重量%、成分(e)を0.1〜5重量%、成分(f)を0.1
〜3重量%含有する、前記潤滑剤。
1. A (a) natural oils, synthetic oils and base oils selected from the group consisting of a mixture thereof, (b) has a density d 20 of at least 0.900, and at least one fourth in the molecule At least one tetravalent to octavalent alcohol derivative containing a secondary carbon atom, wherein the alcohol is selected from the group consisting of mono-, di- and tripentaerythritol, wherein the alcoholic group has 6 to 18 carbon atoms. (C) sterically hindered phenols, (c) sterically hindered phenols, all etherified by alkyl or aryl halides containing straight or branched alkyl, aralkyl or aryl groups having atoms. At least one dialkyldithiocarbamate compound represented by the following formula: (In the formula, Me is a metal selected from the group consisting of boron, vanadium, chromium, molybdenum, tungsten, manganese, cobalt, nickel and mixtures thereof, and R independently has 4 to 8 carbon atoms. (E) at least one compound selected from the group consisting of dialkylaryl phosphites, monoalkyldiaryl phosphites, trialkyl phosphites and triaryl phosphites (provided that the alkyl group is linear, A phenyl group which is branched or cyclic and contains 8 to 12 carbon atoms, and the aryl group is substituted at the o- or p-position by an alkyl group having 1 to 6 carbon atoms. (F) a thiazole derivative, (g) at least one dialkyldithiophosphate represented by the following formula: Compounds, and (In the formula, Me is a metal selected from the group consisting of zinc, molybdenum and a mixture thereof, and R is an alkyl group having 4 to 8 carbon atoms.) (H) Antioxidant, metal inert Selected from agents, detergents, dispersants, defoamers and viscosity index improvers;
(G) a lubricant containing an additive different from any of (g), wherein the component (b) is added in an amount of 0.1 to 4 based on the weight of the component (a);
0% by weight, the total amount of component (d) and component (g) is 0.5 to 10
% By weight, 0.1 to 5% by weight of the component (e), 0.1% by weight of the component (f).
The above-mentioned lubricant containing about 3% by weight.
【請求項2】成分(d)が、ホウ素−ジアルキルジチオ
カルバメート、ニッケル−ジアルキルジチオカルバメー
ト、コバルト−ジアルキルジチオカルバメート、モリブ
テン−ジアルキルジチオカルバメート及びその混合物か
らなる群から選ばれ、成分(g)が、亜鉛−ジアルキル
ジチオホスファート、モリブテン−ジアルキルジチオホ
スファート及びその混合物からなる群から選ばれる、請
求項1記載の潤滑剤。
2. Component (d) is selected from the group consisting of boron-dialkyldithiocarbamate, nickel-dialkyldithiocarbamate, cobalt-dialkyldithiocarbamate, molybten-dialkyldithiocarbamate and mixtures thereof, and component (g) is The lubricant of claim 1, wherein the lubricant is selected from the group consisting of zinc-dialkyldithiophosphate, molybten-dialkyldithiophosphate, and mixtures thereof.
【請求項3】成分(d)が、(i)ホウ素−トリス−ジ
イソブチルジチオカルバメート、ホウ素−トリス−ジ−
2−エチルヘキシルジチオカルバメート及びその混合物
からなる群から選ばれた化合物と共に、(ii)ニッケル
−トリス−ジイソブチルジチオカルバメート、ニッケル
−トリス−ジアミルジチオカルバメート、ニッケル−ト
リス−ジ−2−エチルヘキシルジチオカルバメート及び
その混合物からなる群から選ばれた化合物を含み、成分
(g)が、亜鉛−ビス−ジ−2−エチルヘキシルジチオ
ホスファート、モリブテン−テトラキス−ジ−2−エチ
ルヘキシルジチオホスファート、モリブテン−オキシテ
トラキス−ジ−2−エチルヘキシルジチオホスファート
及びその混合物からなる群から選ばれる、請求項2記載
の潤滑剤。
3. Component (d) is (i) boron-tris-diisobutyldithiocarbamate, boron-tris-di-
(Ii) nickel-tris-diisobutyldithiocarbamate, nickel-tris-diamyldithiocarbamate, nickel-tris-di-2-ethylhexyldithiocarbamate, and a compound selected from the group consisting of 2-ethylhexyldithiocarbamate and a mixture thereof. A compound selected from the group consisting of the mixture thereof, wherein component (g) is zinc-bis-di-2-ethylhexyldithiophosphate, molybten-tetrakis-di-2-ethylhexyldithiophosphate, molybten-oxytetrakis-phosphate. 3. The lubricant of claim 2, wherein the lubricant is selected from the group consisting of di-2-ethylhexyl dithiophosphate and mixtures thereof.
【請求項4】成分(a)の重量を基準にして、0.1〜20
重量%の成分(b)を含有する、請求項1記載の潤滑
剤。
4. The composition according to claim 1, wherein the weight of component (a) is 0.1 to 20.
The lubricant according to claim 1, which contains component (b) by weight.
【請求項5】成分(a)の重量を基準にして、1〜12重
量%の成分(b)を含有する、請求項4記載の潤滑剤。
5. The lubricant according to claim 4, which comprises from 1 to 12% by weight of component (b), based on the weight of component (a).
【請求項6】成分(a)の重量を基準にして、2〜6重
量%の成分(b)を含有する、請求項5記載の潤滑剤。
6. A lubricant according to claim 5, comprising 2 to 6% by weight of component (b), based on the weight of component (a).
【請求項7】基油が、20℃で0.1mPa.s〜2,000,000mPa.s
の範囲内の粘度を有する、請求項1記載の潤滑剤。
7. The base oil has a viscosity of 0.1 mPa.s to 2,000,000 mPa.s at 20 ° C.
The lubricant according to claim 1, having a viscosity in the range of:
【請求項8】合成油が、芳香族ジカルボン酸エステル、
脂肪族ジカルボン酸エステル及びその混合物からなる群
から選ばれる、請求項1記載の潤滑剤。
8. A synthetic oil comprising an aromatic dicarboxylic acid ester,
The lubricant according to claim 1, wherein the lubricant is selected from the group consisting of an aliphatic dicarboxylic acid ester and a mixture thereof.
【請求項9】合成油が、1000〜3000の範囲内の分子量を
有するポリ−α−オレフィン−ジカルボン酸エステルで
ある、請求項8記載の潤滑剤。
9. The lubricant according to claim 8, wherein the synthetic oil is a poly-α-olefin-dicarboxylic acid ester having a molecular weight in the range of 1,000 to 3,000.
【請求項10】合成油が、フタル酸ジイソデシルエステ
ル、トリメチルアジピン酸ジデシルエステル及びセバシ
ン酸ジオクチルエステル、1000〜100,000の分子量及び1
00℃で200mPa.s〜43000mPa.sの粘度を有するポリイソブ
チレン、100℃で1000mPa.sの粘度を有するポリメタクリ
レート、100℃で5mPa.s〜60mPa.sの粘度を有する水に不
溶性のポリグリコール、イソパラフィン油、50℃より高
い引火点と20℃で1.0mPa.s〜2,000,000mPa.sの範囲内の
粘度を有するアルキルベンゼン、及びテロメル酸エステ
ルからなる群から選ばれる、請求項1記載の潤滑剤。
10. The synthetic oil comprises diisodecyl phthalate, didecyl trimethyladipate and dioctyl sebacate, a molecular weight of 1,000 to 100,000 and a molecular weight of 1 to 100,000.
Polyisobutylene having a viscosity of 200 mPa.s to 43000 mPa.s at 00 ° C., polymethacrylate having a viscosity of 1000 mPa.s at 100 ° C., and a water-insoluble polyglycol having a viscosity of 5 mPa.s to 60 mPa.s at 100 ° C. The lubricant of claim 1, wherein the lubricant is selected from the group consisting of isoparaffin oil, an alkylbenzene having a flash point above 50 ° C. and a viscosity at 20 ° C. in the range of 1.0 mPa.s to 2,000,000 mPa.s, and a telomerate. .
【請求項11】天然油が鉱油である、請求項1記載の潤
滑剤。
11. The lubricant according to claim 1, wherein the natural oil is a mineral oil.
JP50365188A 1987-04-10 1988-04-11 Lubricant or lubricant concentrate Expired - Fee Related JP3211959B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19873712134 DE3712134A1 (en) 1987-04-10 1987-04-10 LUBRICANTS OR LUBRICANT CONCENTRATE
DE3712134.0 1987-04-10

Publications (2)

Publication Number Publication Date
JPH01503545A JPH01503545A (en) 1989-11-30
JP3211959B2 true JP3211959B2 (en) 2001-09-25

Family

ID=6325306

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Application Number Title Priority Date Filing Date
JP50365188A Expired - Fee Related JP3211959B2 (en) 1987-04-10 1988-04-11 Lubricant or lubricant concentrate

Country Status (7)

Country Link
EP (1) EP0286140B1 (en)
JP (1) JP3211959B2 (en)
AT (1) ATE111150T1 (en)
CA (1) CA1339121C (en)
DE (2) DE3712134A1 (en)
ES (1) ES2063742T3 (en)
WO (1) WO1988008022A1 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06200270A (en) * 1992-12-29 1994-07-19 Tonen Corp Lubricant composition for final reduction gear
WO1995019411A1 (en) * 1994-01-13 1995-07-20 Mobil Oil Corporation Additives for lubricants
US5500107A (en) * 1994-03-15 1996-03-19 Betz Laboratories, Inc. High temperature corrosion inhibitor
TW340870B (en) * 1995-04-07 1998-09-21 Nippon Nogen Co Ltd Lubricating oil additive, lubricating oil and working fluid for refrigerators
CA2223256A1 (en) * 1995-08-30 1997-03-06 Hirotaka Tomizawa Lubricating oil composition
WO1997015644A1 (en) * 1995-10-23 1997-05-01 Nsk Ltd. Lubricant composition
GB9813071D0 (en) 1998-06-17 1998-08-19 Exxon Chemical Patents Inc Lubricant compositions
EP3476922B1 (en) 2016-06-23 2021-08-25 JXTG Nippon Oil & Energy Corporation Grease composition for constant velocity joints, and constant velocity joint in which same is sealed

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1543830A (en) * 1966-11-10 1968-10-25 Mobil Oil Corp Lubricating compositions containing advanced anti-corrosion additives
US3843542A (en) * 1972-07-31 1974-10-22 Chevron Res Hydraulic oil
FR2467186A1 (en) * 1979-10-15 1981-04-17 Elf France ALKYL ETHERS OF POLYOLS, THEIR PREPARATION AND THEIR JOBS
AT381719B (en) * 1979-10-15 1986-11-25 Elf France LUBRICANTS OR LUBRICANT ADDITIVES
GB2065148A (en) * 1979-12-14 1981-06-24 Cooper & Co Ltd Edwin Lubricating composition
JPS5861189A (en) * 1981-10-07 1983-04-12 Hitachi Ltd Lubricant composition for plastic working
JPS5975995A (en) * 1982-10-25 1984-04-28 Showa Shell Sekiyu Kk Lubricating composition excellent in resistance to wear and extreme pressure and friction properties
FR2540104B1 (en) * 1983-02-01 1987-07-17 Elf France SYNTHESIS OF POLYOL ETHERS

Also Published As

Publication number Publication date
JPH01503545A (en) 1989-11-30
DE3712134C2 (en) 1993-07-15
CA1339121C (en) 1997-07-29
DE3851356D1 (en) 1994-10-13
EP0286140B1 (en) 1994-09-07
WO1988008022A1 (en) 1988-10-20
ES2063742T3 (en) 1995-01-16
ATE111150T1 (en) 1994-09-15
EP0286140A1 (en) 1988-10-12
DE3712134A1 (en) 1988-10-27

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