JP2000345178A - Heat-resistant lubricant composition and grease - Google Patents

Heat-resistant lubricant composition and grease

Info

Publication number
JP2000345178A
JP2000345178A JP16277399A JP16277399A JP2000345178A JP 2000345178 A JP2000345178 A JP 2000345178A JP 16277399 A JP16277399 A JP 16277399A JP 16277399 A JP16277399 A JP 16277399A JP 2000345178 A JP2000345178 A JP 2000345178A
Authority
JP
Japan
Prior art keywords
alkyl
grease
formula
substituted
heat
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
JP16277399A
Other languages
Japanese (ja)
Inventor
Tamio Akata
民生 赤田
Yoshinobu Fujii
祥伸 藤井
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.)
Matsumura Oil Research Corp
Original Assignee
Matsumura Oil Research Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Matsumura Oil Research Corp filed Critical Matsumura Oil Research Corp
Priority to JP16277399A priority Critical patent/JP2000345178A/en
Publication of JP2000345178A publication Critical patent/JP2000345178A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a heat-resistant lubricant composition which comprises the mixture of a specific alkyl-substituted diphenylsulfide with a specified alkyl- substituted diphenylether and can also be applied to lubricating greases used for bearings, gears, and the like, in industrial machines. SOLUTION: This composition comprises the mixture of (A) an alkyl- substituted diphenylsulfide of formula I [R1, R2 are each a 10 to 20C hydrocarbon; 1<=(m)+(n)<=-4] with (B) an alkyl-substituted diphenylether preferably in a component A/B weight ratio of 40/60 to 80/20. It is preferable that the component A or the mixture of the component A with the component B is used as a base oil in a grease comprising the base oil, a thickener and additives.

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、耐熱性潤滑油組成
物に関し、さらに詳しくは、ジフェニルスルフィドのア
ルキル置換体とジフェニルエーテルのアルキル置換体の
混合油からなる耐熱性潤滑油組成物に関し、種々の産業
用機械における軸受、歯車などに用いられる潤滑グリー
スにも適用できる耐熱性潤滑油組成物に関するものであ
る。
The present invention relates to a heat-resistant lubricating oil composition, and more particularly to a heat-resistant lubricating oil composition comprising a mixed oil of an alkyl-substituted diphenyl sulfide and an alkyl-substituted diphenyl ether. The present invention relates to a heat-resistant lubricating oil composition applicable to lubricating grease used for bearings, gears and the like in industrial machines.

【0002】[0002]

【従来の技術】近年、各種機械、軸受の小型軽量化、運
転の高速化、メンテナンスフリー化に伴ない、潤滑油、
潤滑グリースは高温、高速、高荷重といった過酷な条件
のもとで使用されるようになっているため、より優れた
耐熱性および耐酸化性の潤滑油が不可欠になっている。
例えば軸受潤滑において、使用条件が高温、高速になっ
た場合、潤滑に用いられるグリースは油膜切れによる温
度上昇や、高温条件による熱、酸化劣化を引き起こし、
スラッジの生成、さらには軸受の破損、機械の寿命の低
下につながる。このため高温条件下で使用可能な潤滑グ
リースは種々検討されており、一般的には高温条件での
改良はグリースの組成中、最も多く含有する基油と熱、
酸化劣化を防止する酸化防止剤によるところが大きい。
2. Description of the Related Art In recent years, with the reduction in the size and weight of various machines and bearings, the speeding up of operation, and the maintenance-free operation, lubricating oil,
Since lubricating greases are used under severe conditions such as high temperature, high speed and high load, lubricating oils having better heat resistance and oxidation resistance are indispensable.
For example, in bearing lubrication, when the operating conditions are high temperature and high speed, the grease used for lubrication causes temperature rise due to oil film breakage, heat and oxidative deterioration due to high temperature conditions,
This leads to sludge formation, further damage to bearings, and a reduction in machine life. For this reason, various lubricating greases that can be used under high-temperature conditions have been studied.Generally, improvement under high-temperature conditions is based on the most common base oil, heat,
This is largely due to antioxidants that prevent oxidative degradation.

【0003】[0003]

【発明が解決しようとする課題】このような耐熱性に優
れた基油としては、ポリフェニルエーテル、シリコーン
油、フッ素油などが知られている。しかし、ポリフェニ
ルエーテル、フッ素油は非常に高価であり、シリコーン
油は一般に潤滑性に難点があるといわれている。基油の
価格と性能のバランスは、安価で高性能のグリースを提
供する上で重要であり、最近では、アルキル化ジフェニ
ルエーテルを基油として用いる耐熱性グリースが知られ
ている。アルキル化ジフェニルエーテルは、熱・酸化安
定性に優れ、特に高温条件下での使用において蒸発量が
少なく、粘度変化が小さいことなどが特長である。この
ような特性は、他の汎用合成潤滑油、例えば、α−オレ
フィンオリゴマー、アルキルベンゼン、ポリアルキレン
グリコール、エステル系油では得られにくいため、比較
的安価で優れた耐熱性グリースを提供することができ
る。
As such base oils having excellent heat resistance, polyphenyl ether, silicone oil, fluorine oil and the like are known. However, polyphenyl ether and fluorine oil are very expensive, and silicone oil is generally said to have a problem in lubricity. The balance between the price and the performance of the base oil is important in providing an inexpensive and high-performance grease. Recently, a heat-resistant grease using an alkylated diphenyl ether as a base oil has been known. Alkylated diphenyl ethers are excellent in thermal and oxidative stability, and are characterized by a small amount of evaporation and a small change in viscosity particularly when used under high temperature conditions. Such properties are difficult to obtain with other general-purpose synthetic lubricating oils, for example, α-olefin oligomers, alkylbenzenes, polyalkylene glycols, and ester-based oils, so that a relatively inexpensive and excellent heat-resistant grease can be provided. .

【0004】しかし、アルキル化ジフェニルエーテルを
潤滑グリース基油として用いた場合、耐摩耗性に特に優
れた性質はなく、鉱物油やα−オレフィンオリゴマーの
ような炭化水素油と同等であるといえる。したがって、
耐熱性と潤滑性が同時に要求される高速、高荷重での軸
受の運転などでは耐熱性に問題がないにもかかわらず、
優れた潤滑性が得られないために、時には機械の作動時
に異常音を発生するなどの欠点があった。その解決策と
して潤滑性に優れたエステル系油などと混合して使用す
るなどの手法がとられているが、アルキル化ジフェニル
エーテルの配合割合を少なくすると、アルキル化ジフェ
ニルエーテルの持つ優れた耐熱、耐酸化性が損なわれる
ことがしばしばあった。
[0004] However, when an alkylated diphenyl ether is used as a lubricating grease base oil, it does not have particularly excellent wear resistance and can be said to be equivalent to hydrocarbon oils such as mineral oils and α-olefin oligomers. Therefore,
Despite the fact that there is no problem with heat resistance in high-speed, high-load bearing operation, etc., where heat resistance and lubricity are simultaneously required,
Since excellent lubricity cannot be obtained, there have been drawbacks such as an abnormal sound sometimes generated during operation of the machine. A solution to this problem is to use a mixture with an ester oil that has excellent lubricating properties.However, if the proportion of the alkylated diphenyl ether is reduced, the superior heat resistance and oxidation resistance of the alkylated diphenyl ether are obtained. Sex was often impaired.

【0005】今後、機械、軸受などの軽量化、小型化、
メンテナンスフリー化によってグリース潤滑の条件はさ
らに高温、高荷重、高速化するとともに、軸受寿命の延
長、さらには、機械の作動時の異音の撲滅が顧客満足度
の観点からも重要な課題となることが予測される。これ
らに対応するためには、潤滑グリースに用いる増ちょう
剤の種類や酸化防止剤、耐摩耗防止剤、極圧剤、防錆剤
などの各種添加剤の配合技術によってグリースの性能を
補うことができるが、その性能はグリース組成中に最も
多くを占める基油の性能によって大きく左右される。
In the future, the weight and size of machines and bearings will be reduced.
The maintenance-free grease lubrication conditions will be higher temperatures, higher loads, and higher speeds. In addition, extending bearing life and eliminating abnormal noise during machine operation will be important issues from the viewpoint of customer satisfaction. It is expected that. In order to cope with these problems, it is necessary to supplement the performance of the grease with the type of thickener used for lubricating grease and the compounding technology of various additives such as antioxidants, anti-wear agents, extreme pressure agents, rust inhibitors, etc. Although possible, its performance is greatly influenced by the performance of the base oil, which is the largest component in the grease composition.

【0006】本発明の課題は、高温、高速、高荷重な
ど、より厳しい条件下で使用されるグリースに対応する
ために、耐熱、耐酸化性が優れ、かつ潤滑性に優れた耐
熱性潤滑油組成物及びグリースを提供することにある。
An object of the present invention is to provide a heat-resistant lubricating oil which is excellent in heat resistance, oxidation resistance and lubricity in order to cope with grease used under severe conditions such as high temperature, high speed and high load. It is to provide a composition and a grease.

【0007】[0007]

【課題を解決するための手段】本発明は、式(1)で表
されるジフェニルスルフィドのアルキル置換体及び式
(2)で表されるジフェニルエーテルのアルキル置換体
の混合物からなる耐熱性潤滑油組成物に係る。
SUMMARY OF THE INVENTION The present invention provides a heat-resistant lubricating oil composition comprising a mixture of an alkyl-substituted diphenyl sulfide represented by the formula (1) and an alkyl-substituted diphenyl ether represented by the formula (2). Pertaining to things.

【0008】[0008]

【化3】 (式中、RおよびRは炭素数10〜20の炭化水素
基であり、RおよびR は互いに同一であっても異な
るものであってもよい。また、m、nは、1≦m+n≦
4を満たす0以上の整数を示す。)
Embedded image(Where R1And R2Is a hydrocarbon having 10 to 20 carbon atoms
And R is1And R 2Are the same but different
May be used. Also, m and n are 1 ≦ m + n ≦
Indicates an integer of 0 or more that satisfies 4. )

【0009】[0009]

【化4】 (式中、R、R、m、nは上記に同じ。)Embedded image (In the formula, R 1 , R 2 , m, and n are the same as above.)

【0010】また本発明は基油、増ちょう剤及び添加剤
からなるグリースにおいて、基油として式(1)のジフ
ェニルスルフィドのアルキル置換体を使用することを特
徴とするグリース、又は基油、増ちょう剤及び添加剤か
らなるグリースにおいて、基油として式(1)のジフェ
ニルスルフィドのアルキル置換体及び式(2)のジフェ
ニルエーテルのアルキル置換体の混合物を使用すること
を特徴とするグリースに係る。
The present invention also relates to a grease comprising a base oil, a thickener and an additive, characterized in that an alkyl-substituted diphenyl sulfide of the formula (1) is used as the base oil. A grease comprising a thickener and an additive, wherein a mixture of an alkyl-substituted diphenyl sulfide of the formula (1) and an alkyl-substituted diphenyl ether of the formula (2) is used as the base oil.

【0011】本発明は、所定化学構造のアルキル化ジフ
ェニルスルフィド及びアルキル化ジフェニルエーテルを
併用したことにより、アルキル化ジフェニルエーテル固
有の耐熱、耐酸化性以上の安定性を発揮し、優れた耐
熱、耐酸化性を有するだけでなく、特に特定の併用割合
で上記アルキル化ジフェニルスルフィド及びアルキル化
ジフェニルエーテルを用いることにより、各単独よりも
更に優れた熱安定性を示す相乗効果を発揮する耐熱性潤
滑油を提供し、特に高温で使用される潤滑グリースに好
適に用いられるものである。
According to the present invention, an alkylated diphenyl sulfide and an alkylated diphenyl ether having a predetermined chemical structure are used in combination to exhibit stability higher than the heat resistance and oxidation resistance inherent to alkylated diphenyl ether, and provide excellent heat resistance and oxidation resistance. In addition to providing a heat-resistant lubricating oil exhibiting a synergistic effect exhibiting even better thermal stability than each alone by using the above-mentioned alkylated diphenyl sulfide and alkylated diphenyl ether particularly at a specific combination ratio. Particularly, it is suitably used for lubricating grease used at high temperatures.

【0012】[0012]

【発明の実施の形態】本発明のアルキル化ジフェニルス
ルフィドは、一般的な有機合成の手法を用いて合成する
ことが可能である。例えば、出発原料として、ジフェニ
ルスルフィドとα−オレフィンを用いて、反応触媒とし
て塩化アルミニウムなどのルイス酸系均一触媒や、活性
白土などの固体酸不均一触媒などの一般的な芳香環核ア
ルキル化触媒を用いることによって容易に付加反応が進
行する。反応で用いるジフェニルスルフィドとα−オレ
フィンの使用割合は、目的化合物、反応に用いる触媒と
反応条件に応じて変えることができる。無水塩化アルミ
ニウムを用いた場合、反応後、反応混合物にアルカリ中
和剤および活性白土を加えて攪拌した後、ろ過、蒸留を
行うことによって目的化合物を得ることができる。得ら
れた化合物は目的に応じて、さらに活性白土を用いて脱
色処理することができる。
BEST MODE FOR CARRYING OUT THE INVENTION The alkylated diphenyl sulfide of the present invention can be synthesized by using a general organic synthesis technique. For example, using a diphenyl sulfide and an α-olefin as starting materials, a general aromatic ring nucleus alkylation catalyst such as a Lewis acid-based homogeneous catalyst such as aluminum chloride or a solid acid heterogeneous catalyst such as activated clay as a reaction catalyst. The addition reaction easily proceeds by using. The ratio of diphenyl sulfide and α-olefin used in the reaction can be changed according to the target compound, the catalyst used in the reaction and the reaction conditions. When anhydrous aluminum chloride is used, an alkali neutralizer and activated clay are added to the reaction mixture after the reaction, followed by stirring, followed by filtration and distillation to obtain the target compound. The obtained compound can be further subjected to a decolorization treatment using activated clay according to the purpose.

【0013】このようにして得られたアルキル化ジフェ
ニルスルフィドは、他の特徴を付与することを目的に鉱
物油の他、α−オレフィンオリゴマー、ポリオールエス
テル、ジエステル、ポリアルキレングリコール、アルキ
ルベンゼン、アリキルナフタレンなどの合成油と混合し
て使用することも可能である。
[0013] The alkylated diphenyl sulfide thus obtained may be used in addition to mineral oil, α-olefin oligomers, polyol esters, diesters, polyalkylene glycols, alkylbenzenes, alialkylnaphthalenes for the purpose of imparting other characteristics. It is also possible to mix and use with synthetic oils such as.

【0014】本発明で用いるアルキル化ジフェニルスル
フィドは、前記式(1)で示されるものであるが、炭素
数8〜24の炭化水素基としては、直鎖状または分岐状
のアルキル基が挙げられる。好ましい炭化水素基は、炭
素数10〜20のアルキル基であり、その具体例として
は、デシル基、ウンデシル基、ドデシル基、トリデシル
基、テトラデシル基、ンタデシル基、ヘキサデシル基、
ヘプタデシル基、オクタデシル基、ノナデシル基、エイ
コシル基などがあり、これらの分岐を有するものであっ
てもよい。炭素数が10に達しない炭化水素基の場合、
アルキル化ジフェニルスルフィドの蒸発量が多くなりす
ぎ、炭素数が20を超える場合には、流動点が高くなり
すぎる。なお、このような炭化水素基は、2つの芳香環
を有するジフェニルスルフィドのいずれの芳香環のいず
れの位置に結合したものであってもよい。また、ジフェ
ニルスルフィドに対して、付与する炭化水素基の個数
は、前記式(1)のnとmの合計が1〜4が好ましく、
4より大きい場合には、酸化安定性が低下し、炭化水素
基がないと、蒸気圧が高くなりすぎる。
The alkylated diphenyl sulfide used in the present invention is represented by the above formula (1). Examples of the hydrocarbon group having 8 to 24 carbon atoms include a linear or branched alkyl group. . Preferred hydrocarbon groups are alkyl groups having 10 to 20 carbon atoms, specific examples of which are decyl, undecyl, dodecyl, tridecyl, tetradecyl, untadecyl, hexadecyl,
There are a heptadecyl group, an octadecyl group, a nonadecyl group, an eicosyl group and the like, and those having these branches may be used. In the case of a hydrocarbon group having less than 10 carbon atoms,
When the amount of evaporation of the alkylated diphenyl sulfide becomes too large and the number of carbon atoms exceeds 20, the pour point becomes too high. In addition, such a hydrocarbon group may be bonded to any position of any aromatic ring of diphenyl sulfide having two aromatic rings. Further, the number of hydrocarbon groups to be provided to diphenyl sulfide is preferably such that the sum of n and m in the formula (1) is 1 to 4,
If it is larger than 4, the oxidative stability decreases, and if there is no hydrocarbon group, the vapor pressure becomes too high.

【0015】本発明で用いるジフェニルエーテルの炭化
水素置換体は、芳香環を酸素原子で結合した化学構造を
有する周知のアルキル化ジフェニルエーテル油を使用す
ることができるが、ジフェニルエーテル1分子当り、1
〜4のアルキル基を結合した炭化水素体が好ましく、そ
のような炭化水素基としては、直鎖状または分岐状のア
ルキル基であって炭素数が8〜24、特に12〜18の
ものが好ましい。
As the hydrocarbon-substituted diphenyl ether used in the present invention, a known alkylated diphenyl ether oil having a chemical structure in which an aromatic ring is bonded by an oxygen atom can be used.
Hydrocarbons having an alkyl group of from 4 to 4 are preferable, and such a hydrocarbon group is preferably a linear or branched alkyl group having 8 to 24 carbon atoms, particularly preferably 12 to 18 carbon atoms. .

【0016】本発明の耐熱性潤滑油組成物は、その組成
(配合割合)において、ジフェニルスルフィドのアルキ
ル置換体95〜5重量%、ジフェニルエ−テルのアルキ
ル置換体5〜95重量%、を混合する。ジフェニルスル
フィドのアルキル置換体とジフェニルエ−テルのアルキ
ル置換体を上記配合割合で混合することにより、所望の
粘度の潤滑油基油を得ることができる。この混合基油の
耐熱性は、各々単独で用いた場合より改善され、耐酸化
性、耐摩耗性もさらに向上させることができる。
In the heat-resistant lubricating oil composition of the present invention, 95 to 5% by weight of an alkyl-substituted product of diphenyl sulfide and 5-95% by weight of an alkyl-substituted product of diphenyl ether are mixed in the composition (blending ratio). I do. By mixing the alkyl-substituted product of diphenyl sulfide and the alkyl-substituted product of diphenyl ether in the above mixing ratio, a lubricating base oil having a desired viscosity can be obtained. The heat resistance of this mixed base oil is improved as compared with the case of using each alone, and the oxidation resistance and the wear resistance can be further improved.

【0017】より好ましい混合割合は、ジフェニルスル
フィドのアルキル置換体40〜80重量%、ジフェニル
エ−テルのアルキル置換体20〜60重量%である。こ
の場合は実施例から明らかなように ジフェニルスルフ
ィドのアルキル置換体及びジフェニルエ−テルのアルキ
ル置換体のいずれよりも優れた熱安定性を示し、相乗的
効果を発揮する。本発明の耐熱性潤滑油組成物には、必
要に応じて耐摩耗剤、極圧剤、酸化防止剤、粘度指数向
上剤、流動点降下剤、腐食防止剤、防錆剤などの添加剤
を配合したものであってもよい。
More preferably, the mixing ratio is 40 to 80% by weight of an alkyl-substituted diphenyl sulfide and 20 to 60% by weight of an alkyl-substituted diphenyl ether. In this case, as is clear from the examples, both of the alkyl-substituted product of diphenyl sulfide and the alkyl-substituted product of diphenyl ether show superior thermal stability and exhibit a synergistic effect. The heat-resistant lubricating oil composition of the present invention may optionally contain additives such as an antiwear agent, an extreme pressure agent, an antioxidant, a viscosity index improver, a pour point depressant, a corrosion inhibitor and a rust inhibitor. It may be blended.

【0018】このようにして得られる耐熱性潤滑油組成
物は、高温条件で使用されるグリース基油、ジェットエ
ンジン油、耐熱断熱エンジン油、ガスタービン油、無段
変速機油、拡散ポンプ油、ロータリポンプ油、含油プラ
スチック油、含油軸受油、ギヤ油、軸受油、油圧作動液
等として使用可能である。本発明の耐熱性潤滑油組成物
を基油として、これに増ちょう剤、添加剤を配合してグ
リースを得ることができる。
The heat-resistant lubricating oil composition thus obtained can be used under high-temperature conditions, such as grease base oil, jet engine oil, heat-insulated engine oil, gas turbine oil, continuously variable transmission oil, diffusion pump oil, rotary oil It can be used as pump oil, oil-impregnated plastic oil, oil-impregnated bearing oil, gear oil, bearing oil, hydraulic fluid and the like. Grease can be obtained by using the heat-resistant lubricating oil composition of the present invention as a base oil and blending it with a thickener and an additive.

【0019】本発明においては、上記基油として式
(1)のジフェニルスルフィドのアルキル置換体または
式(1)のジフェニルスルフィドのアルキル置換体及び
式(2)のジフェニルエーテルのアルキル置換体の混合
物を使用することができる。この場合は実施例から明ら
かなよう、特に機械の作動時の異音の発生がなく極めて
優れている。式(1)の化合物と式(2)の化合物を併
用する場合は、式(1)の化合物と式(2)の化合物の
比率が、重量比で40/60〜80/20とするのが好
適である。増ちょう剤としては、例えば金属セッケン、
ベントナイト、シリカゲル、銅フタロシアニン、アリル
尿素等を例示できる。添加剤としては例えば酸化防止
剤、防錆剤等を例示できる。
In the present invention, an alkyl-substituted diphenyl sulfide of the formula (1) or a mixture of an alkyl-substituted diphenyl sulfide of the formula (1) and an alkyl-substituted diphenyl ether of the formula (2) is used as the base oil. can do. In this case, as is apparent from the embodiment, there is no generation of abnormal noise particularly during operation of the machine, which is excellent. When the compound of the formula (1) and the compound of the formula (2) are used in combination, the weight ratio of the compound of the formula (1) to the compound of the formula (2) should be 40/60 to 80/20. It is suitable. As a thickener, for example, metal soap,
Bentonite, silica gel, copper phthalocyanine, allyl urea and the like can be exemplified. Examples of the additive include an antioxidant and a rust inhibitor.

【0020】[0020]

【実施例】以下に実施例を挙げて説明するが、なんらこ
れに限定されるものではない。
EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited thereto.

【0021】参考例1 攪拌機、滴下ロート、温度計、冷却管および窒素ガス導
入管を取りつけた容積10Lの四つ口フラスコに、ジフ
ェニルスルフィド2700g(14.5モル)と無水塩
化アルミニウム54g(0.4モル)を入れ、窒素雰囲
気下、70℃に加熱攪拌して触媒を溶解したのち、反応
系の温度を160℃に上げた。窒素流通下、上記反応系
中に、1−ドデセン3013g(18モル)と1−テト
ラデセン2367g(12モル)の混合物を、約120
分かけて滴下し、付加反応を行った。滴下終了後、さら
に160℃で30分間攪拌を続けたのち、反応混合物の
温度が90℃になるまで自然冷却し、アルカリ中和剤3
0gと活性白土30gを投入し、温度を80〜90℃に
保ったまま90分間、加熱攪拌した。続いて、50℃ま
で自然冷却したのち、減圧濾過し、次いで減圧蒸留し
て、未反応の原料およびモノアルキル付加体を除去し、
ジアルキルおよびトリアルキル付加体からなるジフェニ
ルスルフィドの炭化水素置換体3402gを得た。この
合成油を耐熱性潤滑油Aとする。
Reference Example 1 In a 10-liter four-necked flask equipped with a stirrer, a dropping funnel, a thermometer, a cooling tube and a nitrogen gas inlet tube, 2700 g (14.5 mol) of diphenyl sulfide and 54 g (0.4 g) of anhydrous aluminum chloride were placed. 4 mol), and the mixture was heated and stirred at 70 ° C. in a nitrogen atmosphere to dissolve the catalyst, and then the temperature of the reaction system was raised to 160 ° C. Under a nitrogen flow, a mixture of 3013 g (18 mol) of 1-dodecene and 2367 g (12 mol) of 1-tetradecene was introduced into the above reaction system for about 120 minutes.
The mixture was added dropwise over a period of minutes to perform an addition reaction. After completion of the dropwise addition, the mixture was further stirred at 160 ° C. for 30 minutes, and then naturally cooled until the temperature of the reaction mixture reached 90 ° C.
Then, 0 g and 30 g of activated clay were added, and the mixture was heated and stirred for 90 minutes while maintaining the temperature at 80 to 90 ° C. Subsequently, the mixture was naturally cooled to 50 ° C., filtered under reduced pressure, and then distilled under reduced pressure to remove unreacted raw materials and monoalkyl adducts.
3,402 g of a hydrocarbon-substituted product of diphenyl sulfide comprising a dialkyl and trialkyl adduct was obtained. This synthetic oil is referred to as heat-resistant lubricating oil A.

【0022】参考例2 実施例1と同様の装置を用いて、容積10Lの四つ口フ
ラスコに、ジフェニルエーテル1702g(10モル)
と無水塩化アルミニウム37g(0.28モル)を入れ
加熱攪拌して触媒を溶解した。窒素流通下、上記反応系
中に、1−ドデセン2016g(12モル)と1−テト
ラデセン1568g(8モル)の混合物を、約1時間で
滴下して付加反応を行った。滴下中の温度は、110〜
120℃に保持した。滴下終了後、さらに30分間攪拌
を続けたのち、反応混合物の温度が90℃になるまで自
然冷却し、アルカリ中和剤20gと活性白土20gを投
入し、温度を80〜90℃に保ったまま90分間、加熱
攪拌した。続いて、50℃まで自然冷却したのち、減圧
ろ過し、次いで減圧蒸留して、未反応の原料およびモノ
アルキル付加体を除去し、ジアルキルおよびトリアルキ
ル付加体からなるジフェニルエーテルの炭化水素置換体
2618gを得た。この合成油を耐熱性潤滑油Bとす
る。
Reference Example 2 Using a device similar to that of Example 1, 1702 g (10 mol) of diphenyl ether was placed in a four-necked flask having a volume of 10 L.
And 37 g (0.28 mol) of anhydrous aluminum chloride, and the mixture was heated and stirred to dissolve the catalyst. Under a nitrogen stream, a mixture of 2016 g (12 mol) of 1-dodecene and 1568 g (8 mol) of 1-tetradecene was dropped into the above reaction system in about 1 hour to carry out an addition reaction. The temperature during dropping is 110-
It was kept at 120 ° C. After completion of the dropwise addition, the mixture was further stirred for 30 minutes, and then naturally cooled until the temperature of the reaction mixture reached 90 ° C., 20 g of an alkali neutralizer and 20 g of activated clay were added, and the temperature was maintained at 80 to 90 ° C. The mixture was heated and stirred for 90 minutes. Subsequently, after natural cooling to 50 ° C., the mixture was filtered under reduced pressure, and then distilled under reduced pressure to remove unreacted raw materials and monoalkyl adducts. Obtained. This synthetic oil is referred to as heat-resistant lubricating oil B.

【0023】実施例1〜6及び比較例1〜2 耐熱性潤滑油Aと耐熱性潤滑油Bを、表1〜2に示す配
合割合(重量%)で混合して潤滑油組成物を調製した。
得られた潤滑油組成物について、一般性状として引火
点、流動点、40℃および100℃における動粘度、粘
度指数を測定し、これらの結果を表1中に併記した。ま
た、得られた潤滑油組成物について、下記の方法で熱安
定性試験を行い、これらの結果を表1〜2中に併記し
た。 熱安定性試験 ガラス製カップに試料油50gを秤量し、200℃に保
持した恒温槽に20日間静置し、蒸発量(質量%)の経
時変化および試験後の試料油の状態を観察した。
Examples 1 to 6 and Comparative Examples 1 to 2 Heat-resistant lubricating oil A and heat-resistant lubricating oil B were mixed in the proportions (% by weight) shown in Tables 1 and 2 to prepare lubricating oil compositions. .
About the obtained lubricating oil composition, a flash point, a pour point, a kinematic viscosity at 40 ° C. and 100 ° C., and a viscosity index were measured as general properties, and these results are also shown in Table 1. Further, a thermal stability test was performed on the obtained lubricating oil composition by the following method, and these results are also shown in Tables 1 and 2. Thermal Stability Test 50 g of the sample oil was weighed into a glass cup, and allowed to stand in a thermostat kept at 200 ° C. for 20 days, and the time-dependent change in the amount of evaporation (% by mass) and the state of the sample oil after the test were observed.

【0024】[0024]

【表1】 [Table 1]

【0025】[0025]

【表2】 [Table 2]

【0026】表1〜2の結果から明らかなように、実施
例1から6の組成物は、比較例2のアルキル化ジフェニ
ルエーテルと、ほぼ同様の一般性状値を有しているにも
かかわらず、耐熱性、耐酸化性は格段に優れたものであ
った。実施例1〜3においては、ジフェニルスルフィド
の炭化水素置換体を、アルキル化ジフェニルエーテルに
混合することにより、高温における蒸発量変化に相乗効
果がみられ、ジフェニルスルフィドの炭化水素置換体と
アルキル化ジフェニルエーテルの各々を単独で用いた場
合より、優れた耐熱性があった。以上のように、ジフェ
ニルスルフィドの炭化水素置換体を、アルキル化ジフェ
ニルエーテルに混合した組成物は、一般に耐熱性潤滑油
として、高温条件下で汎用的に使用されているアルキル
化ジフェニルエーテルに比べ、優れた耐熱、耐酸化性を
有しており、特に高温下で使用される各種潤滑油として
満足できるものであった。
As is evident from the results in Tables 1 and 2, the compositions of Examples 1 to 6 have almost the same general properties as the alkylated diphenyl ether of Comparative Example 2, Heat resistance and oxidation resistance were remarkably excellent. In Examples 1 to 3, by mixing the hydrocarbon-substituted diphenyl sulfide with the alkylated diphenyl ether, a synergistic effect was observed on the change in the amount of evaporation at high temperature, and the hydrocarbon-substituted diphenyl sulfide and the alkylated diphenyl ether were mixed. There was better heat resistance than when each was used alone. As described above, a composition obtained by mixing a hydrocarbon-substituted diphenyl sulfide with an alkylated diphenyl ether is generally superior as a heat-resistant lubricating oil to an alkylated diphenyl ether generally used under high-temperature conditions. It had heat resistance and oxidation resistance, and was particularly satisfactory as various lubricating oils used at high temperatures.

【0027】実施例7 実施例1の耐熱性潤滑油A(1570g)に、12−ヒ
ドロキシステアリン酸リチウム260gを加えて、攪拌
しながら加熱した後、ステンレス製容器に注入し、冷却
後3本ロールにより1回ミーリングを行った。これに上
記の耐熱性潤滑油Aを170g追加し、3本ロールによ
り2回ミーリングを行って、リチウム石鹸グリースを得
た。
Example 7 260 g of lithium 12-hydroxystearate was added to the heat-resistant lubricating oil A of Example 1 (1570 g), heated with stirring, poured into a stainless steel container, cooled, and then rolled with three rolls. Was performed once. 170 g of the above-mentioned heat-resistant lubricating oil A was added thereto, and milling was performed twice using three rolls to obtain a lithium soap grease.

【0028】実施例8 実施例7の操作を用いて、表3に示す組成のグリースを
調製した。各グリースの混和ちょう度、滴点、離油度を
測定した結果を表3に併記した。さらに、下記の方法
で、潤滑性試験を行い、これらの結果も表3に併記し
た。
Example 8 Using the procedure of Example 7, a grease having the composition shown in Table 3 was prepared. Table 3 also shows the results of measuring the penetration, dropping point, and oil release of each grease. Further, a lubricity test was conducted by the following method, and these results are also shown in Table 3.

【0029】比較例3 実施例7の操作を用いて、耐熱性潤滑油Bを基油とする
グリースを調製した。 潤滑性試験 高速四球試験機を用いて、回転数1200rpm、負荷
荷重40kgfで、室温下で1時間運転し、試験中の異
常音の発生有無と試験後の摩耗痕径を観察した。
Comparative Example 3 Using the procedure of Example 7, a grease using a heat-resistant lubricating oil B as a base oil was prepared. Lubricity Test Using a high-speed four-ball testing machine, the system was operated at room temperature for 1 hour at a rotational speed of 1200 rpm and a load of 40 kgf, and the occurrence of abnormal noise during the test and the wear scar diameter after the test were observed.

【0030】[0030]

【表3】 [Table 3]

【0031】表3から明らかなように、比較例3は、潤
滑性試験において、試験中、潤滑性不良による異常音が
発生したのに対し、実施例7,8のグリースでは、異常
音の発生はなく、摩耗痕径も、汎用的にグリース基油と
して使用されているアルキル化ジフェニルエーテルを基
油とした比較例3のグリースより小さく、ジフェニルス
ルフィドのアルキル置換体を用いた組成物は、グリース
の基油に適用できるものであった。
As is clear from Table 3, in the lubricating test, in the lubricating test, abnormal noise due to poor lubrication was generated, whereas in the greases of Examples 7 and 8, abnormal noise was generated. No, the wear scar diameter is smaller than the grease of Comparative Example 3 using an alkylated diphenyl ether as a base oil which is widely used as a grease base oil, and the composition using an alkyl-substituted diphenyl sulfide is It could be applied to base oils.

【0032】[0032]

【発明の効果】本発明は、以上説明したように、ジフェ
ニルスルフィドのアルキル置換体とジフェニルエーテル
のアルキル置換体を併用したことにより、ジフェニルエ
ーテルのアルキル置換体固有の耐熱性、耐酸化性以上の
性能を発揮し、優れた耐熱性潤滑油となるという利点が
ある。更にジフェニルスルフィドのアルキル置換体とジ
フェニルエーテルのアルキル置換体を特定の割合で併用
することにより、ジフェニルスルフィドのアルキル置換
体及びジフェニルエーテルのアルキル置換体のいずれよ
りも優れた熱安定性を示し、相乗的効果を発揮する。
As described above, according to the present invention, by using an alkyl-substituted diphenyl sulfide and an alkyl-substituted diphenyl ether in combination, the heat resistance and the oxidation resistance inherent to the alkyl-substituted diphenyl ether are improved. It has the advantage of exhibiting excellent heat-resistant lubricating oil. Furthermore, the combined use of the alkyl-substituted diphenyl sulfide and the alkyl-substituted diphenyl ether at a specific ratio shows superior thermal stability to both the alkyl-substituted diphenyl sulfide and the alkyl-substituted diphenyl ether, and a synergistic effect. Demonstrate.

【0033】さらに、ジフェニルスルフィドのアルキル
置換体又は、ジフェニルスルフィドのアルキル置換体及
びジフェニルエ−テルのアルキル置換体の混合物をグリ
ース基油として用いた場合、従来のアルキル化ジフェニ
ルエーテルを基油としたグリースに見られる異常音が発
生せず、優れたグリース用基油を提供することができ
る。
Further, when an alkyl-substituted diphenyl sulfide or a mixture of an alkyl-substituted diphenyl sulfide and an alkyl-substituted diphenyl ether is used as a grease base oil, a conventional grease using an alkylated diphenyl ether as a base oil is used. The grease base oil can be provided without generating the abnormal noise shown in FIG.

───────────────────────────────────────────────────── 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) C10N 50:10 Fターム(参考) 4H104 BB08A BG15A EB06 EB09 EB10 LA04 LA05 PA01 PA02 PA03 PA05 PA07 PA20 PA41 QA18 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI theme coat ゛ (reference) C10N 50:10 F term (reference) 4H104 BB08A BG15A EB06 EB09 EB10 LA04 LA05 PA01 PA02 PA03 PA05 PA07 PA20 PA41 QA18

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 式(1)で表されるジフェニルスルフィ
ドのアルキル置換体及び式(2)で表されるジフェニル
エーテルのアルキル置換体の混合物からなる耐熱性潤滑
油組成物。 【化1】 (式中、RおよびRは炭素数10〜20の炭化水素
基であり、RおよびR は互いに同一であっても異な
るものであってもよい。また、m、nは、1≦m+n≦
4を満たす0以上の整数を示す。) 【化2】 (式中、R、R、m、nは上記に同じ。)
1. A diphenyl sulphide represented by the formula (1)
Substituted alkyl and diphenyl represented by the formula (2)
Heat-resistant lubrication consisting of a mixture of alkyl-substituted ethers
Oil composition. Embedded image(Where R1And R2Is a hydrocarbon having 10 to 20 carbon atoms
And R is1And R 2Are the same but different
May be used. Also, m and n are 1 ≦ m + n ≦
Indicates an integer of 0 or more that satisfies 4. )(Where R1, R2, M and n are the same as above. )
【請求項2】 式(1)の化合物と式(2)の化合物の
比率が、重量比で40/60〜80/20である請求項
1記載の耐熱性潤滑油組成物。
2. The heat-resistant lubricating oil composition according to claim 1, wherein the ratio of the compound of the formula (1) to the compound of the formula (2) is 40/60 to 80/20 by weight.
【請求項3】 基油、増ちょう剤及び添加剤からなるグ
リースにおいて、基油として式(1)のジフェニルスル
フィドのアルキル置換体を使用することを特徴とするグ
リース。
3. A grease comprising a base oil, a thickener and an additive, characterized in that an alkyl-substituted diphenyl sulfide of the formula (1) is used as the base oil.
【請求項4】 基油、増ちょう剤及び添加剤からなるグ
リースにおいて、基油として式(1)のジフェニルスル
フィドのアルキル置換体及び式(2)のジフェニルエー
テルのアルキル置換体の混合物を使用することを特徴と
するグリース。
4. A grease comprising a base oil, a thickener and an additive, wherein a mixture of an alkyl-substituted diphenyl sulfide of the formula (1) and an alkyl-substituted diphenyl ether of the formula (2) is used as the base oil. Grease characterized by the following.
【請求項5】 式(1)の化合物と式(2)の化合物の
比率が、重量比で40/60〜80/20である請求項
4記載のグリース。
5. The grease according to claim 4, wherein the ratio of the compound of the formula (1) to the compound of the formula (2) is 40/60 to 80/20 by weight.
JP16277399A 1999-06-09 1999-06-09 Heat-resistant lubricant composition and grease Pending JP2000345178A (en)

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Country Link
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002338981A (en) * 2001-05-16 2002-11-27 Furukawa Electric Co Ltd:The Corrosion-proof transmission wire and corrosion-proofing heat-resistant grease used therefor
WO2005040081A1 (en) * 2003-10-23 2005-05-06 Matsumura Oil Research Corp. Alkyl-substituted diphenyl ether compound and composition containing the same
JP2012102051A (en) * 2010-11-10 2012-05-31 Moresco Corp Alkylated diphenyl ether and lubricant agent containing the compound
WO2014069669A1 (en) * 2012-10-31 2014-05-08 株式会社Moresco Alkylated diphenyl ether compound and lubricating oil containing said compound
WO2014069670A1 (en) * 2012-10-31 2014-05-08 株式会社Moresco Alkylated diphenyl ether compound and lubricating oil containing said compound

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002338981A (en) * 2001-05-16 2002-11-27 Furukawa Electric Co Ltd:The Corrosion-proof transmission wire and corrosion-proofing heat-resistant grease used therefor
WO2005040081A1 (en) * 2003-10-23 2005-05-06 Matsumura Oil Research Corp. Alkyl-substituted diphenyl ether compound and composition containing the same
JPWO2005040081A1 (en) * 2003-10-23 2007-03-08 株式会社松村石油研究所 Alkyl-substituted diphenyl ether compounds and compositions containing the same
JP4698422B2 (en) * 2003-10-23 2011-06-08 株式会社Moresco Alkyl substituted diphenyl ether compounds and compositions containing the same
JP2012102051A (en) * 2010-11-10 2012-05-31 Moresco Corp Alkylated diphenyl ether and lubricant agent containing the compound
WO2014069669A1 (en) * 2012-10-31 2014-05-08 株式会社Moresco Alkylated diphenyl ether compound and lubricating oil containing said compound
WO2014069670A1 (en) * 2012-10-31 2014-05-08 株式会社Moresco Alkylated diphenyl ether compound and lubricating oil containing said compound
CN104395274A (en) * 2012-10-31 2015-03-04 株式会社Moresco Alkylated diphenyl ether compound and lubricating oil containing the compound
CN104507900A (en) * 2012-10-31 2015-04-08 株式会社Moresco Alkylated diphenyl ether compound and lubricating oil containing said compound
CN104507900B (en) * 2012-10-31 2016-06-08 株式会社Moresco Alkylated diphenyl ethers compound and the lubricating oils containing this compound
US9561992B2 (en) 2012-10-31 2017-02-07 Moresco Corporation Alkylated diphenyl ether compound and lubricating oil containing said compound
US10487034B2 (en) 2012-10-31 2019-11-26 Moresco Corporation Alkylated diphenyl ether compound and lubricating oil containing said compound

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