JP2011529974A - Lubricating grease composition - Google Patents

Lubricating grease composition Download PDF

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JP2011529974A
JP2011529974A JP2011520423A JP2011520423A JP2011529974A JP 2011529974 A JP2011529974 A JP 2011529974A JP 2011520423 A JP2011520423 A JP 2011520423A JP 2011520423 A JP2011520423 A JP 2011520423A JP 2011529974 A JP2011529974 A JP 2011529974A
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lubricating grease
grease composition
acid
composition according
lithium
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JP2011529974A5 (en
JP5848126B2 (en
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ステファン・ダーグリング
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Shell Internationale Research Maatschappij BV
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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
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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
    • C10M107/30Macromolecular 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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    • C10M117/00Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
    • C10M2207/1236Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic used as thickening agent
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/127Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids polycarboxylic
    • C10M2207/1276Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids polycarboxylic used as thickening agent
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/128Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof
    • C10M2207/1285Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof used as thickening agents
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    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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    • C10M2209/105Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
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    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • C10M2209/107Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
    • C10M2209/1075Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106 used as base material
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    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
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Abstract

(i)ポリアルキレングリコール基油、(ii)リチウム錯体増粘剤、及び(iii)炭素原子数が18以上のカルボン酸を含む潤滑性グリース組成物で、特にデュアル・マス・フライホイールの摩擦低下に有用である。
【選択図】なし
A lubricating grease composition comprising (i) a polyalkylene glycol base oil, (ii) a lithium complex thickener, and (iii) a carboxylic acid having 18 or more carbon atoms, particularly a friction reduction of a dual mass flywheel. Useful for.
[Selection figure] None

Description

発明の分野
本発明は潤滑性グリース組成物、特にフライホール用、特にデュアル・マス・フライホイール(dual mass flywheel)用に使用される潤滑性グリース組成物に関する。
FIELD OF THE INVENTION The present invention relates to a lubricating grease composition, particularly a lubricating grease composition used for flyholes, particularly for dual mass flywheels.

発明の背景
潤滑の主目的は、摩擦及び摩耗を最小にするため、互いに動く固体表面を分離することである。この目的で最も多く使用される材料は油及びグリースである。潤滑剤の選択は殆ど特定の用途により決定される。
BACKGROUND OF THE INVENTION The main purpose of lubrication is to separate solid surfaces that move with each other to minimize friction and wear. The most frequently used materials for this purpose are oils and greases. The choice of lubricant is largely determined by the specific application.

デュアル・マス・フライホイールは、過剰な変速ギアのがたつき音をなくし、ギアチェンジ/シフト労力(effort)を減らし、また燃料経済性を向上させる。デュアル・マス・フライホイールは、駆動列(drive train)での振動を弱めるため、通常、標準的手動変速機付き軽量ディーゼルトラックや高性能の高級車に取り付けられている。これにより、自動車を長期間、損傷なく操作できる。   The dual mass flywheel eliminates excessive rattling gear shifting, reduces gear change / shift effort, and improves fuel economy. Dual mass flywheels are usually mounted on lightweight diesel trucks with standard manual transmissions or high-end luxury cars to damp vibrations in the drive train. As a result, the automobile can be operated for a long time without damage.

リチウム石鹸錯体を基材とするグリースは、フライホイール用に使用されることが知られている。このようなグリースでは十分な潤滑特性が得られることが判っている。しかし、高性能に対する要求はますます増大しているので、潤滑特性、特に摩擦低下特性が向上したデュアル・マス・フライホイール用グリースを提供することが望ましい。   It is known that greases based on lithium soap complexes are used for flywheels. Such greases have been found to provide sufficient lubrication characteristics. However, as the demand for high performance is increasing, it is desirable to provide a dual mass flywheel grease with improved lubrication properties, particularly friction reduction properties.

本発明によれば、(i)ポリアルキレングリコール基油、(ii)リチウム錯体増粘剤、及び(iii)炭素原子数が18以上のカルボン酸を含む潤滑性グリース組成物が提供される。   According to the present invention, there is provided a lubricating grease composition comprising (i) a polyalkylene glycol base oil, (ii) a lithium complex thickener, and (iii) a carboxylic acid having 18 or more carbon atoms.

更に本発明によれば、前述の潤滑性グリース組成物をデュアル・マス・フライホイール用に使用する方法が提供される。   Further in accordance with the present invention, there is provided a method of using the aforementioned lubricating grease composition for a dual mass flywheel.

更に本発明によれば、摩擦を低下させるため、前述の潤滑性グリース組成物を使用する方法が提供される。   Further in accordance with the present invention, there is provided a method of using the lubricating grease composition described above to reduce friction.

本発明のグリース組成物は優れた摩擦低下特性を示すと共に、良好な安定性、良好な耐摩耗特性、高度の耐遠心力性、及びグリース寿命の増大を示すことが意外にも見出された。   It was unexpectedly found that the grease composition of the present invention exhibits excellent friction reducing properties, as well as good stability, good wear resistance, high centrifugal resistance, and increased grease life. .

発明の詳細な説明
本発明の潤滑性グリースは必須成分としてポリアルキレングリコール基油を含有する。
本発明の潤滑性グリース組成物に使用されるポリアルキレングリコール基油については特別な制限はなく、従来の各種ポリアルキレングリコールが都合良く使用できる。
本発明で使用されるポリアルキレングリコール(PAG)は、モノマー単位として炭素原子数が1〜6のアルキレンオキシド(−R−O−)を示すことができる。
DETAILED DESCRIPTION OF THE INVENTION The lubricating grease of the present invention contains a polyalkylene glycol base oil as an essential component.
The polyalkylene glycol base oil used in the lubricating grease composition of the present invention is not particularly limited, and various conventional polyalkylene glycols can be conveniently used.
The polyalkylene glycol (PAG) used in the present invention can represent an alkylene oxide (—R—O—) having 1 to 6 carbon atoms as a monomer unit.

ポリアルキレングリコールは、水素末端基、アルキル、アリール、アルキルアリール、アルコキシ、アルキルアリールオキシ及び/又はヒドロキシ末端基を示すことができる。アルキルアリールオキシ基は、アリールアルキル(エン)基(例えばアリールCHCH−を意味するため、アリールアルキル(エン)オキシ基及びアルキルアリール基を意味するとも理解してよい。アルコキシ型を含むアルキル型の末端基、又はアルキルアリール型、アリールオキシ型及びアルキルアリールオキシ型の末端基は、アリール型に対し炭素原子数が好ましくは6〜24、特に好ましくは6〜18、及びアルキル型に対し炭素原子数が好ましくは1〜12を表す。 The polyalkylene glycol can exhibit hydrogen end groups, alkyl, aryl, alkylaryl, alkoxy, alkylaryloxy and / or hydroxy end groups. An alkylaryloxy group may also be understood to mean an arylalkyl (ene) group (eg, arylCH 2 CH 2 —, thus meaning an arylalkyl (ene) oxy group and an alkylaryl group. The terminal group of the type, or the terminal group of the alkylaryl type, aryloxy type and alkylaryloxy type preferably has 6 to 24 carbon atoms, particularly preferably 6 to 18 carbon atoms for the aryl type and carbon for the alkyl type. The number of atoms is preferably 1-12.

ここで使用されるポリアルキレングリコールの密度は、本組成物に使用されるリチウム錯体石鹸(例えばセバシン酸リチウム、アゼライン酸リチウム)の密度と同様であることが好ましい。ここで使用されるポリアルキレングリコールの密度は、好ましくは900〜1400kg/m、更に好ましくは950〜1100kg/m、なお更に好ましくは1000〜1100kg/mである。 It is preferable that the density of the polyalkylene glycol used here is the same as the density of the lithium complex soap (for example, lithium sebacate, lithium azelate) used in the present composition. The density of the polyalkylene glycol used here is preferably 900 to 1400 kg / m 3 , more preferably 950 to 1100 kg / m 3 , and still more preferably 1000 to 1100 kg / m 3 .

均質重合体、即ち、ポリアルキレングリコール(及び/又はポリプロピレンオキシド)か、又は共重合体、三元共重合体等であってよい。後者の場合、モノマー単位は、ランダム分布又はブロック構造を表してよい。ポリアルキレングリコールが非均質重合体でなければ、全モノマー単位の好ましくは20%以上、好ましくは40%以上は、ポリプロピレンオキシド(PO)から製造でき、またこれらポリアルキレングリコールの全モノマー単位の好ましくは20%以上は、エチレンオキシド(EO)を用いて製造できる(PO/EO共重合体)。更なる実施態様では、全モノマー単位の好ましくは20%以上、好ましくは40%以上は、ブチレンオキシド(BO)を用いて得られ、更にこれらポリアルキレングリコールの全モノマー単位の好ましくは20%以上は、エチレンオキシド(EO)を用いて得られる(BO/EO共重合体)。   It may be a homogeneous polymer, ie, a polyalkylene glycol (and / or polypropylene oxide), or a copolymer, terpolymer, and the like. In the latter case, the monomer units may represent a random distribution or block structure. If the polyalkylene glycol is not a heterogeneous polymer, preferably 20% or more, preferably 40% or more of the total monomer units can be produced from polypropylene oxide (PO), and preferably the total monomer units of these polyalkylene glycols are preferably More than 20% can be produced using ethylene oxide (EO) (PO / EO copolymer). In a further embodiment, preferably more than 20%, preferably more than 40% of the total monomer units are obtained using butylene oxide (BO), more preferably more than 20% of the total monomer units of these polyalkylene glycols. , Obtained using ethylene oxide (EO) (BO / EO copolymer).

ここでの好ましい実施態様では、全モノマー単位の好ましくは50%以上、好ましくは80%以上は、プロピレンオキシドから製造でき、残部はエチレンオキシドで製造できる。
ここでの特に好ましい実施態様ではポリアルキレングリコールはプロピレンオキシドの均質重合体である。ポリプロピレン均質重合体の例は、ダウケミカルから商品名Synalox(登録商標)、例えばSynalox(登録商標)100−150Bで市販されている。
In a preferred embodiment here, preferably 50% or more, preferably 80% or more of the total monomer units can be produced from propylene oxide and the remainder can be produced from ethylene oxide.
In a particularly preferred embodiment here, the polyalkylene glycol is a homopolymer of propylene oxide. Examples of polypropylene homopolymers are commercially available from Dow Chemical under the trade name Synalox®, such as Synalox® 100-150B.

(ポリ)アルコールを使用する場合、出発化合物は本発明の意味に従って、この重合体鎖の末端基とも言われる、重合体の末端に取り込まれる。好適な出発群(starting groups)は、活性水素含有化合物からなる。活性水素含有化合物は例えば水、n−ブタノール、プロピレングリコール、エチレングリコール、ペンタエリスリトールのようなネオペンチルグリコール、エチレンジアミン、フェノール、クレゾール又は他の(C〜C16(モノ、ジ又はトリ)アルキル)芳香族、(ヒドロキシアルキル)芳香族、ハイドロキノン、アミノエタノールアミン、トリエチレンテトラミン、ポリアミン、ソルビトール又は他の糖類である。カルボン酸又はカルボン酸無水物のような他のC−H酸性化合物も出発化合物として使用できる。他の好適な出発化合物の例としてはC10〜C18アルコールのような長鎖アルコールが含まれる。 When a (poly) alcohol is used, the starting compound is incorporated at the end of the polymer, also referred to as the end group of this polymer chain, according to the meaning of the present invention. Preferred starting groups consist of active hydrogen-containing compounds. Active hydrogen-containing compounds, for example water, n- butanol, propylene glycol, ethylene glycol, neopentyl glycols such as pentaerythritol, ethylene diamine, phenol, cresol or other (C 1 ~C 16 (mono-, di- or tri) alkyl) Aromatic, (hydroxyalkyl) aromatic, hydroquinone, aminoethanolamine, triethylenetetramine, polyamine, sorbitol or other sugars. Other CH acidic compounds such as carboxylic acids or carboxylic anhydrides can also be used as starting compounds. Examples of other suitable starting compounds include long chain alcohols such as C 10 -C 18 alcohol.

ポリアルキレングリコールは、例えば重合体鎖に側基又は末端基として挿入されたアリール基又は複素芳香族基に相当する基を有する。これらの基は、必要ならば直鎖又は分岐アルキル基又はアルキレン基で置換してよい。これらのアルキル基又はアルキレン基全体は好ましくは炭素原子数1〜18のものを表す。   The polyalkylene glycol has, for example, a group corresponding to an aryl group or heteroaromatic group inserted as a side group or terminal group into the polymer chain. These groups may be substituted with linear or branched alkyl groups or alkylene groups if necessary. These whole alkyl groups or alkylene groups preferably represent those having 1 to 18 carbon atoms.

ヒドロキシフルフリル又はヒドロキシテトラヒドロフラン、窒素複素環式化合物又は硫黄複素環式化合物のような環式エーテルアルコールも出発化合物群として使用できる。このようなポリアルキレングリコールはWO 01/57164に開示されている。この文献の教示はここに援用する。   Cyclic ether alcohols such as hydroxyfurfuryl or hydroxytetrahydrofuran, nitrogen heterocyclic compounds or sulfur heterocyclic compounds can also be used as a starting compound group. Such polyalkylene glycols are disclosed in WO 01/57164. The teachings of this document are incorporated herein.

本発明のポリアルキレングリコールは、平均分子量(数平均)が好ましくは200〜6000g/モル、更に好ましくは400〜4000g/モル、なお更に好ましくは1000〜3000g/モル、特に2000〜3000g/モルのものである。   The polyalkylene glycol of the present invention preferably has an average molecular weight (number average) of 200 to 6000 g / mol, more preferably 400 to 4000 g / mol, still more preferably 1000 to 3000 g / mol, and particularly 2000 to 3000 g / mol. It is.

本発明で使用されるポリアルキレングリコールは、出発化合物として、ポリアルコールを含むアルコールを、エチレンオキシド、プロピレンオキシド及び/又はブチレンオキシドのようなオキシランと反応させて製造できる。この反応に従って、ポリアルキレングリコールは末端基として遊離のヒドロキシル基を1個しか持たない。ヒドロキシル基を1個しか持たないポリアルキレングリコールは、遊離のヒドロキシル基を2個有するポリアルキレングリコールよりも好ましい。例えば更なるエーテル化工程後は、もはや遊離のヒドロキシル基を含まないポリアルキレングリコールは、安定性、吸湿性及び相溶性の点で特に好ましい。末端ヒドロキシル基のアルキル化により熱安定性が増大する。したがって、本発明の特に好ましい実施態様では、PAG基油は、末端封鎖した、即ち、遊離のヒドロキシル基が存在しないPAGを含む。   The polyalkylene glycol used in the present invention can be produced by reacting an alcohol containing a polyalcohol as a starting compound with an oxirane such as ethylene oxide, propylene oxide and / or butylene oxide. According to this reaction, the polyalkylene glycol has only one free hydroxyl group as a terminal group. Polyalkylene glycols having only one hydroxyl group are preferred over polyalkylene glycols having two free hydroxyl groups. For example, after further etherification steps, polyalkylene glycols which no longer contain free hydroxyl groups are particularly preferred in terms of stability, hygroscopicity and compatibility. Alkylation of the terminal hydroxyl group increases thermal stability. Thus, in a particularly preferred embodiment of the invention, the PAG base oil comprises a PAG that is end-capped, ie, free of free hydroxyl groups.

潤滑性組成物は、PAG基油を潤滑性組成物の総量に対し30重量%以上、好ましくは50重量%以上、更に好ましくは70重量%以上含有することが好ましい。基油として(1種又はそれ以上の)基油だけを使用することがなお更に好ましい。   The lubricating composition contains PAG base oil in an amount of 30% by weight or more, preferably 50% by weight or more, more preferably 70% by weight or more based on the total amount of the lubricating composition. It is even more preferred to use only the base oil (one or more) as the base oil.

本発明の好ましい実施態様ではPAG基油の40℃での動粘度(ASTM D445による)は、32〜690mm/s、好ましくは100〜300mm/s、更に好ましくは150〜250mm/sである。 In a preferred embodiment of the present invention, the PAG base oil has a kinematic viscosity at 40 ° C. (according to ASTM D445) of 32 to 690 mm 2 / s, preferably 100 to 300 mm 2 / s, more preferably 150 to 250 mm 2 / s. is there.

ポリアルキレングリコール基油の他、従来使用されているいずれの鉱物又は合成源であってよい別の基油を含有できる。しかし、本発明の好ましい実施態様では、基油は1種以上のポリアルキレングリコール基油のみからなる。   In addition to the polyalkylene glycol base oil, it may contain other base oils that may be any conventionally used mineral or synthetic source. However, in a preferred embodiment of the present invention, the base oil consists solely of one or more polyalkylene glycol base oils.

鉱物源の基油は、例えば溶剤精製又は水素化処理により製造した鉱油であってよい。合成源の基油は、一般にC10〜50炭化水素重合体の混合物、例えばα−オレフィンの液状重合体の混合物であってよい。これらは従来のエステル、例えばポリオールエステルであってもよい。基油はこれら油の混合物であってもよい。基油はロイヤルダッチ/シェルの企業グループから“HVI”又は“MVIN”の名称で販売されている鉱物源の基油はポリα−オレフィン又はこれら2種の混合物が好ましい。合成炭化水素基油、例えばロイヤルダッチ/シェルの企業グループから“XHVI”の名称で販売されているものも使用できる。グリースの製造に使用される潤滑性鉱油ベース原料が存在すれば、このベース原料はパラフィン系、ナフテン系及び混合系ベース原油から誘導され、従来法で精製した、いかなるベース原料であってもよい。 The mineral source base oil may be, for example, a mineral oil produced by solvent refining or hydroprocessing. The synthetic base oil may generally be a mixture of C10-50 hydrocarbon polymers, such as a liquid polymer mixture of α-olefins. These may be conventional esters such as polyol esters. The base oil may be a mixture of these oils. The base oil is preferably a poly-α-olefin or a mixture of the two, as the mineral source base oil sold under the names “HVI” or “MVIN” by the Royal Dutch / Shell business group. Synthetic hydrocarbon base oils such as those sold under the name “XHVI” by the Royal Dutch / Shell corporate group can also be used. If there is a lubricating mineral oil base stock used in the manufacture of grease, this base stock can be any base stock derived from paraffinic, naphthenic and mixed base crudes and refined by conventional methods.

本発明の潤滑性グリース組成物は、ポリアルキレングリコール基油の他に、更にリチウム石鹸錯体増粘剤を含有する。   The lubricating grease composition of the present invention further contains a lithium soap complex thickener in addition to the polyalkylene glycol base oil.

グリース中に存在するリチウム石鹸錯体の量は、組成物に対し、好ましくは2〜30重量%、好ましくは5〜20重量%である。
好ましい実施態様では、リチウム石鹸錯体は、C12〜C24ヒドロキシ脂肪酸のリチウム石鹸及びC〜C12脂肪族ジカルボン酸のリチウム石鹸を含有する。
The amount of lithium soap complex present in the grease is preferably 2-30% by weight, preferably 5-20% by weight, based on the composition.
In a preferred embodiment, the lithium soap complex contains C 12 -C 24 lithium hydroxy fatty acid soaps and lithium soaps of C 2 -C 12 aliphatic dicarboxylic acids.

更に好ましくはヒドロキシ脂肪酸のリチウム石鹸はC16〜C20ヒドロキシ脂肪酸である。特に好ましいヒドロキシ脂肪酸は、ヒドロキシステアリン酸、例えば9−ヒドロキシ、10−ヒドロキシ又は12−ヒドロキシステアリン酸、更に好ましくは後者である。二重結合が9−10位にある12−ヒドロキシステアリン酸の不飽和形態であるリシノレン酸も使用できる。他の好適なヒドロキシ脂肪酸としては12−ヒドロキシベヘン酸及び10−ヒドロキシパルミチン酸が含まれる。 More preferably, the hydroxy fatty acid lithium soap is a C 16 -C 20 hydroxy fatty acid. Particularly preferred hydroxy fatty acids are hydroxystearic acid, such as 9-hydroxy, 10-hydroxy or 12-hydroxystearic acid, more preferably the latter. Lisinolenic acid, an unsaturated form of 12-hydroxystearic acid with a double bond in the 9-10 position, can also be used. Other suitable hydroxy fatty acids include 12-hydroxybehenic acid and 10-hydroxypalmitic acid.

ジカルボン酸は好ましくはC〜C12、更に好ましくはC〜C10脂肪族ジカルボン酸である。好適な酸の例としては蓚酸、マロン酸、琥珀酸、グルタル酸、アジピン酸、スベリン酸、ピメリン酸、アゼライン酸、ドデカンジオン酸及びセバシン酸が含まれる。アゼライン酸及びセバシン酸が特に好ましい。 Dicarboxylic acid is preferably a C 4 -C 12, more preferably C 6 -C 10 aliphatic dicarboxylic acids. Examples of suitable acids include succinic acid, malonic acid, succinic acid, glutaric acid, adipic acid, suberic acid, pimelic acid, azelaic acid, dodecanedioic acid and sebacic acid. Azelaic acid and sebacic acid are particularly preferred.

12〜C24ヒドロキシ脂肪酸及びC〜C12脂肪族ジカルボン酸は20:1〜1:1、好ましくは10:1〜1:1、更に好ましくは8:1〜3:1の重量比で存在することが好ましい。 C 12 -C 24 hydroxy fatty acid and C 2 -C 12 aliphatic dicarboxylic acid is 20: 1 to 1: 1, preferably 10: 1 to 1: 1, more preferably 8: 1 to 3: 1 by weight Preferably it is present.

本発明潤滑性グリース組成物の他の必須成分は炭素原子数18以上の長鎖カルボン酸である。炭素原子数18以上の長鎖カルボン酸は、組成物に対し0.1〜10重量%、好ましくは約1〜約10重量%、更に好ましくは約1〜約5重量%存在することが好ましい。   Another essential component of the lubricating grease composition of the present invention is a long chain carboxylic acid having 18 or more carbon atoms. The long chain carboxylic acid having 18 or more carbon atoms is preferably present in an amount of 0.1 to 10% by weight, preferably about 1 to about 10% by weight, more preferably about 1 to about 5% by weight, based on the composition.

長鎖カルボン酸は炭素原子数18〜90のカルボン酸から選択される。特に好ましい実施態様では、一般式R(COOH)(但し、nは2又は3であり、Rは炭素原子24〜90、好ましくは36〜54の飽和でも不飽和でもよい炭化水素残基である)の二量体酸及び三量体酸から選ばれる。リノレン酸二量体は、リノレン酸の2分子を通常のディールス・アルダー反応に従って反応させて形成される。リノレン酸三量体は、各リノレン酸の不飽和基により共に連結したリノレン酸の3分子の重合により形成されたC54カルボン酸である。リノレン酸の二量体及び三量体は、Oleon Chemicalsから商品名Radiacidで、またArizona Chemicalsから商品名Unidymeで市販されている。特に好ましいリノレン酸の二量体及び三量体は、ベルギーのOleon Chemicalsから市販されているRadiacid 0975及びRadiacid 0980、並びに米国Arizona Chemicalsから市販されているUnidyme 12(C18二量体)である。 The long chain carboxylic acid is selected from carboxylic acids having 18 to 90 carbon atoms. In a particularly preferred embodiment, the general formula R (COOH) n , where n is 2 or 3, and R is a hydrocarbon residue of 24 to 90 carbon atoms, preferably 36 to 54, which may be saturated or unsaturated. ) Dimer acid and trimer acid. The linolenic acid dimer is formed by reacting two molecules of linolenic acid according to a normal Diels-Alder reaction. Linolenic trisodium mer is a C 54 carboxylic acid that is formed by polymerization of three molecules of linolenic acid linked together by unsaturated groups of each linolenic acid. The dimers and trimers of linolenic acid are commercially available from Oleon Chemicals under the trade name Radiacid and from Arizona Chemicals under the trade name Unidyme. Particularly preferred linolenic acid dimers and trimers are Radiacid 0975 and Radiacid 0980 commercially available from Oleon Chemicals, Belgium, and Unidyme 12 (C 18 dimer) commercially available from Arizona Chemicals, USA.

本発明の潤滑性グリースには、グリースに酸化安定性、粘稠性、極圧性及び耐腐食性のような所望特性を付与するために、従来の各種グリース用添加剤を当該利用分野で使用される量、取り入れてよい。好適な添加剤としては、1種以上の極圧/耐摩耗剤、例えばジアルキル又はジアリールジチオホスフェート、ボレート、置換チアジアゾール、例えばジアルコキシアミンと、置換有機ホスフェート、アミンホスフェート、天然又は合成源の硫酸化鯨油、硫酸化ラード、硫酸化エステル、硫酸化脂肪酸エステル、及び同様な硫酸化材料、例えば式(OR)P=O(但し、Rはアルキル、アリール又はアラルキル基)のオルガノホスフェート、及びトリホスホロチオネートとの反応で作った高分子窒素/燐化合物;カルシウム又はマグネシウムアルキルサリチレート又はアルキルアリールスルホネートのような1種以上の過塩基化金属含有洗浄剤;ポリイソブテニルコハク酸無水物とアミン又はエステルとの反応生成物のような1種以上の無灰分分散剤;ヒンダードフェノール又はアミン、例えばフェニルα−ナフチルアミンのような1種以上の酸化防止剤;1種以上の防錆剤;1種以上の摩擦改質剤;1種以上の粘度指数向上剤;1種以上の流動点降下剤;及び1種以上の粘稠剤が含まれる。グラファイト、微粉砕二硫化モリブデン、タルク、金属粉末、及びポリエチレンワックスのような各種重合体も特種な特性を付与するために添加してよい。 In the lubricating grease of the present invention, various conventional grease additives are used in the application field in order to impart desired properties such as oxidation stability, viscosity, extreme pressure and corrosion resistance to the grease. Can be taken in. Suitable additives include one or more extreme pressure / antiwear agents such as dialkyl or diaryldithiophosphates, borates, substituted thiadiazoles such as dialkoxyamines, and substituted organic phosphates, amine phosphates, sulfation of natural or synthetic sources. Whale oil, sulfated lard, sulfated esters, sulfated fatty acid esters, and similar sulfated materials such as organophosphates of the formula (OR) 3 P = O, where R is an alkyl, aryl or aralkyl group, and triphosphoro Polymeric nitrogen / phosphorus compounds made by reaction with thionate; one or more overbased metal-containing detergents such as calcium or magnesium alkyl salicylates or alkylaryl sulfonates; polyisobutenyl succinic anhydride and One or more non-reactive products such as reaction products with amines or esters Minute dispersants; one or more antioxidants such as hindered phenols or amines such as phenyl α-naphthylamine; one or more rust inhibitors; one or more friction modifiers; one or more viscosity index improvements Agents; one or more pour point depressants; and one or more thickeners. Various polymers such as graphite, finely pulverized molybdenum disulfide, talc, metal powder, and polyethylene wax may also be added to impart special properties.

摩擦レベルを下げるため、当業者はモリブデン系配合物の使用を大いに期待していて、このような潤滑性組成物の特許文献は多数提案されている。
本発明を以下の実施例を参照して説明する。
In order to reduce the friction level, those skilled in the art greatly expect the use of molybdenum-based formulations, and a large number of patent documents on such lubricating compositions have been proposed.
The invention will now be described with reference to the following examples.

実施例1〜3及び比較例A
実施例1〜3及び比較例Aの潤滑性グリースを以下の手順で製造した。
基油の50%を12−ヒドロキシステアリン酸、セバシン酸及び水酸化リチウム一水和物並びに水100mlと一緒にオートクレーブに装入した。オートクレーブを閉じ、145℃まで加熱した。ガス抜き(venting)温度に達してから、ガス抜きバルブを開き、水蒸気を30分間放出した。水蒸気圧が0バールになった時、なおガス抜きバルブを開けた状態で加熱を開始し、215℃とした。215℃の温度に達してから、ジャケットを用いて1℃/分の冷却速度で165℃に達するまで冷却した。165℃に達してから、基油の残りの50%を容器に装入した。次いで生成物を80℃に冷却し、添加剤を容器に装入した。次いで生成物を3本ロールミルで均質化した。
製造したグリースの組成を下記表1に示す。実施例1は不飽和C18脂肪酸の特定の二量体を4%含有する。実施例2は不飽和C18脂肪酸の特定の三量体を4%含有する。実施例3は飽和C18脂肪酸を含有する。比較例AはC18脂肪酸の二量体又は三量体を含有しない。
Examples 1 to 3 and Comparative Example A
The lubricating greases of Examples 1 to 3 and Comparative Example A were produced by the following procedure.
50% of the base oil was charged to the autoclave with 12-hydroxystearic acid, sebacic acid and lithium hydroxide monohydrate and 100 ml of water. The autoclave was closed and heated to 145 ° C. After reaching the venting temperature, the vent valve was opened and water vapor was released for 30 minutes. When the water vapor pressure reached 0 bar, heating was started with the degassing valve still open, and the temperature was 215 ° C. After reaching a temperature of 215 ° C., the jacket was used to cool to 165 ° C. at a cooling rate of 1 ° C./min. After reaching 165 ° C., the remaining 50% of the base oil was charged to the container. The product was then cooled to 80 ° C. and the additive was charged to the container. The product was then homogenized on a three roll mill.
The composition of the manufactured grease is shown in Table 1 below. Example 1 contains 4% of a specific dimer of unsaturated C18 fatty acids. Example 2 contains 4% of a specific trimer of unsaturated C18 fatty acids. Example 3 contains saturated C18 fatty acids. Comparative Example A does not contain a dimer or trimer of C18 fatty acids.

1.ダウケミカルから市販されているポリプロピレングリコール均質重合体
2.Oleon Chemicalsから市販されているC18脂肪酸の二量体
3.Oleon Chemicalsから市販されているC18脂肪酸の三量体
4.Oleon Chemicalsから市販されているC18飽和脂肪酸
5.米国Chemturaの市販品
6.ドイツ、Ludwigshafen、Chemturaの市販品
7.スイスCIBA Geigy Specialtiesの市販品
8.ベルギーCorm Van Loockeの市販品
1. 1. Polypropylene glycol homopolymers available from Dow Chemical 2. Dimer of C18 fatty acid commercially available from Oleon Chemicals. 3. Trimers of C18 fatty acids commercially available from Oleon Chemicals 4. C18 saturated fatty acids commercially available from Oleon Chemicals 5. Commercial product of Chemtura, USA 6. Commercial products from Ludwigshafen, Chemtura, Germany 7. Swiss commercial product of CIBA Geigy Specialties. Commercial products from Belgium, Belgium.

実施例4
摩擦係数の測定
下記試験法を用いて実施例1〜3及び比較例Aの摩擦係数を測定した。
Example 4
Measurement of Friction Coefficient The friction coefficients of Examples 1 to 3 and Comparative Example A were measured using the following test method.

マス・フライホイールの摩擦試験は動的捩り試験装備リグを用いて行った。材料規格と一致しなければならないマス・フライホイールの全ての内部部品には完全な新品を使用する必要がある。マス・フライホイールは一定した表面状態を得るため、動的捩り試験リグ中でまず状態調節される。試験部品の充填指針に従ってマス・フライホイールに(実施例及び比較例の)グリースを充填し、次いで120℃の温度、2000rpm、及び0.25Hzで角度+/−30°の振幅で試験する。マス・フライホイールの摩擦値は、完全な1サイクルに必要なトルクに相当する。摩擦係数は、0交差(zero crossing)での各方向からの変位(displacement)後の最大トルクから、0交差での各方向の再変位(displacement)後の最少トルクを引いて2で割って算出される。実施例1〜3及び比較例Aの摩擦係数を下記表2に示す。   The friction test of the mass flywheel was performed using a rig equipped with a dynamic torsion test. It is necessary to use completely new all internal parts of the mass flywheel that must meet the material standards. The mass flywheel is first conditioned in a dynamic torsion test rig to obtain a constant surface condition. Mass flywheels are filled with grease (in the examples and comparative examples) according to the test part filling guidelines and then tested at a temperature of 120 ° C., 2000 rpm, and 0.25 Hz with an angle of +/− 30 °. The mass flywheel friction value corresponds to the torque required for a complete cycle. The friction coefficient is calculated by subtracting the minimum torque after displacement in each direction at zero crossing from the maximum torque after displacement in each direction at zero crossing and dividing by 2. Is done. The friction coefficients of Examples 1 to 3 and Comparative Example A are shown in Table 2 below.


表2の結果からPAG+リチウム石鹸錯体に二量体(C36)酸又は三量体(C54)酸を添加すると、摩擦係数がかなり低下することが判る。

From the results in Table 2, it can be seen that the addition of dimer (C 36 ) acid or trimer (C 54 ) acid to the PAG + lithium soap complex significantly reduces the coefficient of friction.

WO 01/57164WO 01/57164

Claims (11)

(i)ポリアルキレングリコール基油、(ii)リチウム錯体増粘剤、及び(iii)炭素原子数が18以上のカルボン酸を含む潤滑性グリース組成物。   A lubricating grease composition comprising (i) a polyalkylene glycol base oil, (ii) a lithium complex thickener, and (iii) a carboxylic acid having 18 or more carbon atoms. 前記カルボン酸の炭素原子数が18〜54である請求項1に記載の潤滑性グリース組成物。   The lubricating grease composition according to claim 1, wherein the carboxylic acid has 18 to 54 carbon atoms. 前記カルボン酸が、一般式R(COOH)(但し、nは2又は3であり、Rは炭素原子数36〜54の炭化水素残基である)の二量体酸及び三量体酸から選ばれる請求項1又は2に記載の潤滑性グリース組成物。 The carboxylic acid is derived from dimer acid and trimer acid of the general formula R (COOH) n (where n is 2 or 3 and R is a hydrocarbon residue having 36 to 54 carbon atoms). The lubricating grease composition according to claim 1 or 2, which is selected. 前記カルボン酸が、リノレン酸の二量体又は三量体から選ばれる請求項1〜3のいずれか1項に記載の潤滑性グリース組成物。   The lubricating grease composition according to any one of claims 1 to 3, wherein the carboxylic acid is selected from a dimer or trimer of linolenic acid. 前記リチウム錯体増粘剤が、C12〜C24ヒドロキシカルボン酸のリチウム石鹸及びC〜C12ジカルボン酸のリチウム石鹸を含む請求項1〜4のいずれか1項に記載の潤滑性グリース組成物。 Wherein the lithium complex thickener, lubricating grease composition according to claim 1 comprising a C 12 -C 24 lithium soap of a hydroxy carboxylic acid and lithium soaps of C 2 -C 12 dicarboxylic acids . 前記C12〜C24ヒドロキシカルボン酸のリチウム石鹸が、12−ヒドロキシステアリン酸リチウムである請求項5に記載の潤滑性グリース組成物。 The lubricating grease composition according to claim 5, wherein the C 12 -C 24 hydroxycarboxylic acid lithium soap is lithium 12-hydroxystearate. 前記C〜C12ジカルボン酸が、アゼライン酸、セバチン酸及びそれらの混合物から選ばれる請求項5又は6に記載の潤滑性グリース組成物。 The C 2 -C 12 dicarboxylic acids, azelaic acid, lubricating grease composition according to claim 5 or 6 selected from sebacic acid and mixtures thereof. 前記ポリアルキレングリコール基油がポリプロピレングリコールの均質重合体である請求項1〜7のいずれか1項に記載の潤滑性グリース組成物。   The lubricating grease composition according to any one of claims 1 to 7, wherein the polyalkylene glycol base oil is a homogeneous polymer of polypropylene glycol. 前記ポリアルキレングリコール基油の密度が900〜1400kg/mである請求項1〜8のいずれか1項に記載の潤滑性グリース組成物。 The lubricating grease composition according to any one of claims 1 to 8, wherein the density of the polyalkylene glycol base oil is 900 to 1400 kg / m 3 . 請求項1〜9のいずれか1項に記載の潤滑性グリース組成物をデュアル・マス・フライホイール用に使用する方法。   A method of using the lubricating grease composition according to any one of claims 1 to 9 for a dual mass flywheel. 摩擦を低下させるため、請求項1〜10のいずれか1項に記載の潤滑性グリース組成物を使用する方法。   A method of using the lubricating grease composition according to any one of claims 1 to 10 to reduce friction.
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