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JP2000514853A - Lubricants containing alkyl-substituted naphthalenes and esters - Google Patents

Lubricants containing alkyl-substituted naphthalenes and esters

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Publication number
JP2000514853A
JP2000514853A JP10505719A JP50571998A JP2000514853A JP 2000514853 A JP2000514853 A JP 2000514853A JP 10505719 A JP10505719 A JP 10505719A JP 50571998 A JP50571998 A JP 50571998A JP 2000514853 A JP2000514853 A JP 2000514853A
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JP
Japan
Prior art keywords
lubricant
weight
ester
hours
alkyl
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.)
Ceased
Application number
JP10505719A
Other languages
Japanese (ja)
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JP2000514853A5 (en
Inventor
クリンカー、ランドール
Original Assignee
カストロール、リミテッド
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Application filed by カストロール、リミテッド filed Critical カストロール、リミテッド
Publication of JP2000514853A publication Critical patent/JP2000514853A/en
Publication of JP2000514853A5 publication Critical patent/JP2000514853A5/ja
Ceased legal-status Critical Current

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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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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    • 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
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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
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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
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    • C10M111/00Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
    • C10M111/02Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a non-macromolecular organic compound
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    • C10M149/00Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
    • C10M149/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M149/06Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amido or imido group
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    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
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    • C10M2207/28Esters
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    • C10M2207/28Esters
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

(57)【要約】 アルキル置換ナフタレンとエステルとを含む潤滑剤。   (57) [Summary] A lubricant containing an alkyl-substituted naphthalene and an ester.

Description

【発明の詳細な説明】 アルキル置換ナフタレンとエステルとを含む潤滑剤 この発明は、エステルを含む潤滑剤に関するものである。さらに詳しく言えば 、この発明は、揮発度と機能寿命の改良された高温鎖用オイルに関するものであ る。 駆動用鎖、パーチクルボード用プレス、テンター(幅出機)のフレーム及びス テンター(幅出機)のフレームに使用される潤滑剤組成物は、粘度の安定性を必 要とする。 エステルを含んだこれまでの潤滑剤は、エステルによって経験される高温での 粘度変化のために、高温で駆動用鎖に使用するには満足なものでなかった。ポリ アルファオレフィンを使用している組成物は、エステルによって経験するのと同 じ粘度変化を示さないが、ポリアルファオレフィンを含むオイルは、薄いフィル ム条件の下でワニスを生成する傾向を持つために、満足なものでないことが確か められた。これまでの潤滑剤のその他の欠点は、受け入れることができない揮発 度と不適当な機能寿命とである。 この発明は、エステルを含む潤滑剤組成物にアルキル置換ナフタレンを含ませ ることによって、上述の欠点とその他の不都合とを克服するものである。 この発明の1つの目的は、高温の環境中で作動する駆動用鎖及び他の鎖機構に 使用できる粘度特性の改良された潤滑剤を提供することである。 この発明のもう1つの目的は、揮発特性が改良され、機能寿命が延びた高温で の鎖用オイルを提供することである。 この発明に係る潤滑剤組成物は、アルキル置換ナフタレンとエステルとを含む ものである。アルキル置換ナフタレンと言う場合には、色々な長さを持った1個 又は2個以上の直鎖又は枝分かれしたアルキル基で置換されたナフタレンを指す ものと考えられる。 エステルを含む潤滑剤組成物中に1個又は2個以上のアルキル置換ナフタレン 化合物が含まれると、オイル全体の揮発度が低下するのは勿論、オイルの機能寿 命が伸びるというような、予期しない改良が起こる。 この発明は、潤滑剤組成物の揮発度を改良するに充分な量のアルキル置換ナフ タレンを含んでいる。或いはまた、この発明は、潤滑剤の機能寿命を伸ばすに充 分な量を含んでいる。一般に、アルキル置換ナフタレンは、潤滑剤組成物の約1 0重量%から約50重量%を構成し、或いはまた約12重量%から約30重量% を構成している。特別のことわりがなければ、この明細書のどこでも成分の量は 全組成物の重量%で表示されている。 この発明で用いることのできるエステルは、カーク・オスマーのエンサイクロ ペディア、オブ、ケミカル、テクノロジー(1994年第4版)、第9巻、78 1−812頁に開示されているので、ここではこれを引用して組み入れる。さら に詳述すると、この発明は、ジエステル、フタレート、トリメリテート、ピロメ リテート、ダイマーアシッドエステル、ポリオール及びポリオレートを含んでい てもよい。トリメリト酸エステルとポリオールとが、とくに適していると考えら れる。或る実施態様では、エステルが潤滑剤組成物の約40重量%から約90重 量%までを構成し、或いはまた約50重量%から約80重量%までを構成してい る。 実施例 次の実施例は、この発明の性質を理解するための基礎を提供するものであり、 この発明の範囲を限定するものではない。下記の実施例は色々な等級の粘度を持 ったこの発明の異なった実施態様を表している。 実施例1 実施例2 エムカレート(Emkarate)9130 70% 63.4% モービル(Mobil)MCP968 15% 18% インドポール(Indopol)H−1900 − 16% パラポール(Parapol)13.00 13% − イルガルーブ(Irgalube)349 0.6% 0.6% イルガノックス(Irganox)L06 0.6% 1% バンルーブ(Vanlube)SS 0.4% 0.6% ナサル(Nasul)707 0.4% 0.4% エムカレート9130は、ICIケミカルポリマー社から販売されているトリ メリト酸エステルである。モービルMCP968は、モービル、ケミカル、コン パニイから販売されているジアルキル及びトリアルキルナフタレンの混合物であ る。パラポール1300とインドポールH−1900は、ポリブテンの重合体で ある。イルガルーブ349は、チバガイギーPLCから販売されている耐摩耗性 添加剤である。イルガノックスL06は、またチバガイギーPLCから販売され ている酸化防止剤である。バンルーブSSは、RTバンダービルト、ケミカル、 コーポレイションから販売されている酸化防止剤である。最後に、ナサル707 は、キング、インダストリーズから販売されている防食剤である。 実施例1として記載した実施態様の市販品製造では、上に記載した量のエムカ レート9130とモービルMCP968とを一緒にして約70℃から約85℃の 温度に加熱する。次いで、パラボール1300(又はインドポールH−1900 )と、イルガノックスL06と、バンルーブSSを混合して混合物とする。イル ガノックスL06とバンルーブSSとは粉末であるから、混合物中で溶融しなけ ればならず、さらに混合物はイルガノックスL06とバンルーブSSとが完全に 混 合物中に分散するまで混合されなければならない。その後、この組成物の温度を 約60℃に低下させ、イルガルーブ349とナサル707とを組成物中に混合す る。 上に述べた実施例における潤滑剤組成物のサンプルは、前の段落で概略を説明 した工程に従って製造されたものである。その組成物の揮発度を評価するために 、TAインストルメントにより熱重量分析用にとくに設計された器具中でサンプ ルを一定温度に置いて、数個のサンプルの等温蒸発を測定した。下記の結果中で 、「t90」は元のサンプルの10重量%が蒸発した(すなわち、サンプルの9 0重量%が残っている)時間を表し、また「t50」は元のサンプルの50重量 %が蒸発した(すなわち、サンプルの50重量%が残っている)時間を表してい る。 実施例1 実施例2 200℃ t90 >10時間 >10時間 t50 >10時間 >10時間 225℃ t90 2.2時間 3.5時間 t50 >10時間 >10時間 250℃ t90 0.60時間 1.3時間 t50 3.3時間 5.5時間 275℃ t90 0.31時間 0.35時間 t50 1.3時間 1.3時間 このテスト結果は、この発明の有用で改良された蒸発特性を示している。 この発明のすぐれていることは、実施例1の蒸発特性をアルキルナフタレン化 合物が含まれていないサンプル(組成B)の蒸発特性と比較することによって判 明する。組成Bは次のものからなる。 エムカレート9130 85% モービルMCP968 − パラポール1300 13% イルガルーブ349 0.6% イルガノックスL06 0.6% バンルーブSS 0.4% ナサル707 0.4% 組成Bは、モービルMCP968(ジアルキル及びトリアルキルナフタレンの 混合物)の代わりに、エムカレート9130(トリメリト酸エステル)を余分に 含んでいる点を除けば、実施例1と同じ成分を同量含んでいる。実施例1と組成 Bのサンプル10〜12mgについて、等温走査を4個の異なる温度で行った。 下記の結果は、4個の温度の何れでも元のサンプルの50重量%が蒸発した(す なわち、サンプルの5重量%が残っている)温度を示している。 実施例1 組成B 225℃ t50 >10時間 7時間 250℃ t50 3.3時間 2.4時間 275℃ t51 1.4時間 0.6時間 300℃ t50 0.25時間 0.20時間 どの試験温度においても、実施例1の潤滑剤は、潤滑剤の50%が存在しなく なる程度に蒸発するのに長い時間を必要とした。この結果は、揮発度について、 この発明の改良が広い温度範囲にわたって観察されることを示している。 この発明の潤滑剤組成物は、高温での駆動用鎖の用途において使用の要求を満 たすことができるという点で、注目に値する。しかし、この発明は、また低い揮 発度と長い機能寿命とが望ましいすべての潤滑剤の用途に適していることは勿論 、歯車や空気圧縮機のようなその他の用途にも適している。 上述の明細事項、実施例及びデータは、ここに記載された発明を理解し使用す るための基礎を提供するものである。しかし、ここに記載した範囲内でのこの発 明の実施態様は、この発明の精神と発明の範囲との中に含まれている。DETAILED DESCRIPTION OF THE INVENTION              Lubricants containing alkyl-substituted naphthalenes and esters   The present invention relates to a lubricant containing an ester. More specifically, The present invention relates to a hot chain oil having improved volatility and functional life. You.   Drive chains, particle board presses, tenter frames Lubricant compositions used in tenter frames must have stable viscosity. I need it.   Traditional lubricants containing esters have been used at the high temperatures experienced by esters. Due to viscosity changes, it was not satisfactory for use in drive chains at high temperatures. Poly Compositions using alpha-olefins are similar to those experienced with esters. Oil that does not show the same viscosity change, but contains polyalphaolefin Is likely to be unsatisfactory due to its tendency to produce varnish under ambient conditions Was called. Other disadvantages of previous lubricants are unacceptable volatilization Degree and inadequate functional life.   The present invention provides a lubricant composition containing an ester containing an alkyl-substituted naphthalene. This overcomes the above disadvantages and other disadvantages.   One object of the present invention is to provide a drive chain and other chain mechanisms that operate in a high temperature environment. It is to provide a lubricant with improved viscosity properties that can be used.   It is another object of the present invention to provide a high temperature at elevated temperature with improved volatile properties and extended functional life. Is to provide a chain oil.   The lubricant composition according to the present invention contains an alkyl-substituted naphthalene and an ester Things. When we say alkyl-substituted naphthalene, one with various lengths Or a naphthalene substituted with two or more linear or branched alkyl groups It is considered something.   One or more alkyl-substituted naphthalenes in a lubricant composition containing an ester The inclusion of compounds not only reduces the overall volatility of the oil, but also the functional life of the oil. Unexpected improvements occur, such as extending lives.   The present invention relates to an alkyl-substituted naphne in an amount sufficient to improve the volatility of the lubricant composition. Contains taren. Alternatively, the invention is directed to extending the functional life of the lubricant. Contains a small amount. Generally, the alkyl-substituted naphthalenes comprise about 1 to about 1% of the lubricant composition. From 0% to about 50% by weight, or alternatively from about 12% to about 30% by weight. Is composed. Unless otherwise stated, the amounts of ingredients anywhere in this specification are Expressed as a percentage by weight of the total composition.   Esters which can be used in this invention are Kirk Osmer's encyclopedia. Pedia, of, Chemical, Technology (4th edition of 1994), Vol. 9, 78 Since it is disclosed on page 1-812, it is incorporated herein by reference. Further More specifically, the present invention relates to diesters, phthalates, trimellitates, Contains Retain, Dimer Acid Ester, Polyol and Polyolate You may. Trimellitic acid esters and polyols are considered to be particularly suitable. It is. In some embodiments, the ester comprises from about 40% to about 90% by weight of the lubricant composition. % By weight, or alternatively from about 50% to about 80% by weight. You. Example   The following examples provide a basis for understanding the nature of the invention, It is not intended to limit the scope of the invention. The examples below have various grades of viscosity. 3 illustrates different embodiments of the present invention.                                                 Example 1 Example 2       Emkarate 9130 70% 63.4%       Mobil MCP968 15% 18%       Indopol H-1900-16%       Parapol 13.00 13%-       Irgalube 349 0.6% 0.6%       Irganox L06 0.6% 1%       Vanlube SS 0.4% 0.6%       Nasul 707 0.4% 0.4%   Emcalate 9130 is a commercial product sold by ICI Chemical Polymer. It is a melitate ester. Mobil MCP968 is a mobile, chemical, A mixture of dialkyl and trialkyl naphthalenes sold by Pany You. Parapol 1300 and Indopol H-1900 are polybutene polymers is there. Ilgarve 349 is a wear resistant product sold by Ciba Geigy PLC It is an additive. Irganox L06 is also available from Ciba Geigy PLC Is an antioxidant. VANLUBE SS is RT Vanderbilt, Chemical, It is an antioxidant sold by Corporation. Finally, Nasar 707 Is an anticorrosive sold by King, Industries.   In the commercial production of the embodiment described as Example 1, the amount of emca Rate 9130 and Mobil MCP 968 together at about 70 ° C. to about 85 ° C. Heat to temperature. Then, Paraball 1300 (or Indopol H-1900) ), Irganox L06 and Banlube SS are mixed to form a mixture. Il Since GANOX L06 and Banlube SS are powders, they must be melted in a mixture. In addition, the mixture is completely Irganox L06 and Vanlube SS Mixed Must be mixed until dispersed in the compound. Then, the temperature of the composition Lower to about 60 ° C. and mix Irgarbe 349 and Nasal 707 in the composition You.   A sample of the lubricant composition in the above-described example is outlined in the previous paragraph. It is manufactured according to the steps described above. To evaluate the volatility of the composition Sampling in instruments specially designed for thermogravimetric analysis by TA Instruments The sample was placed at a constant temperature and the isothermal evaporation of several samples was measured. In the results below , “T90” indicates that 10% by weight of the original sample had evaporated (ie, 9% of the sample). 0% by weight) time and "t50" is 50 weight of the original sample Represents the time at which the% has evaporated (ie, 50% by weight of the sample remains). You.                                       Example 1 Example 2        200 ° C t90> 10 hours> 10 hours                    t50> 10 hours> 10 hours        225 ° C t90 2.2 hours 3.5 hours                    t50> 10 hours> 10 hours        250 ° C t90 0.60 hours 1.3 hours                    t50 3.3 hours 5.5 hours        275 ° C t90 0.31 hours 0.35 hours                    t50 1.3 hours 1.3 hours   This test result demonstrates the useful and improved evaporation characteristics of the present invention.   The advantage of this invention is that the evaporation characteristics of Example 1 are The comparison was made with the evaporation characteristics of a sample containing no compound (composition B). I will tell. Composition B consists of:       Emcalate 9130 85%       Mobil MCP968-       Parapole 1300 13%       Ilgarbe 349 0.6%       0.6% of Irganox L06       Banlube SS 0.4%       Nasal 707 0.4%   Composition B comprises Mobil MCP968 (a dialkyl and trialkyl naphthalene) Mixture) instead of emcalate 9130 (trimellitic acid ester) Except for the point, it contains the same components as in Example 1 in the same amounts. Example 1 and composition Isothermal scans were performed at four different temperatures on 10-12 mg of the B sample. The results below show that at all four temperatures 50% by weight of the original sample evaporated (I.e., 5% by weight of the sample remains).                                        Example 1 Composition B        225 ° C t50> 10 hours 7 hours        250 ℃ t50 3.3 hours 2.4 hours        275 ° C t51 1.4 hours 0.6 hours        300 ° C t50 0.25 hours 0.20 hours   At any test temperature, the lubricant of Example 1 had 50% of the lubricant absent. It took a long time to evaporate to some extent. The result is It shows that the improvement of the invention is observed over a wide temperature range.   The lubricant composition of the present invention meets the requirements for use in drive chain applications at high temperatures. It is noteworthy that it can be done. However, this invention also has low volatility. Of course it is suitable for all lubricant applications where power and long service life are desired Also suitable for other applications such as gears and air compressors.   The above specification, examples and data have been used to understand and use the invention described herein. It provides the basis for However, within this range, this The obvious embodiments are included within the spirit and scope of the invention.

【手続補正書】特許法第184条の8第1項 【提出日】平成10年9月18日(1998.9.18) 【補正内容】 補正した請求の範囲 1. アルキル置換ナフタレンとエステルとを含むことを特徴とする鎖用潤滑剤。 2. 潤滑剤が、約10重量%から約50重量%まで、好ましくは約12重量%か ら約30重量%までのアルキル置換ナフタレンを含有することを特徴とする、 請求項1に記載の鎖用潤滑剤。 3. 潤滑剤が、ジエステル、フタレート、トリメリテート、ピロメリテート、ダ イマーアシッドエステル、ポリオール及びポリオレエートから選ばれた少なく とも1つのエステルを含むこどを特徴とする、請求項1又は2に記載の鎖用潤 滑剤。 4. 潤滑剤が、約40重量%から約90重量%まで、好ましくは約50重量%か ら約80重量%までのエステルを含むことを特徴とする、請求項1−3の何れ か1つの項に記載の鎖用潤滑剤。 5. 鎖伝導、パーチクルボードプレス、テンターフレーム及びステンターフレー ム用潤滑剤として、請求項1−4の何れか1つの項に記載の鎖用潤滑剤の使用 。 6. 高温での潤滑剤の揮発度を減少させるために、エステルを含む鎖用潤滑剤中 でのアルキル置換ナフタレンの使用。[Procedure of Amendment] Article 184-8, Paragraph 1 of the Patent Act [Submission date] September 18, 1998 (September 18, 1998) [Correction contents]                            Amended claims 1. A chain lubricant comprising an alkyl-substituted naphthalene and an ester. 2. from about 10% to about 50%, preferably about 12% by weight of the lubricant;   Containing up to about 30% by weight of an alkyl-substituted naphthalene,   The chain lubricant according to claim 1. 3. If the lubricant is diester, phthalate, trimellitate, pyromellitate,   At least one selected from imer acid esters, polyols and polyoleates   3. The chain lubricant according to claim 1, wherein the at least one ester comprises at least one ester.   Lubricant. 4. If the lubricant is from about 40% to about 90% by weight, preferably about 50% by weight.   4. The composition of any of claims 1-3, wherein the ester comprises up to about 80% by weight of an ester.   The chain lubricant according to any one of the above items. 5. Chain conduction, particle board press, tenter frame and stenter frame   Use of the chain lubricant according to any one of claims 1-4 as a system lubricant . 6. In order to reduce the volatility of the lubricant at high temperatures, it is recommended that   Use of alkyl-substituted naphthalenes in the industry.

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Claims (1)

【特許請求の範囲】 1. アルキル置換ナフタレンとエステルとを含むことを特徴とする潤滑剤。 2. 潤滑剤が、約10重量%から約50重量%まで、好ましくは約12重量%か ら約30重量%までのアルキル置換ナフタレンを含有することを特徴とする、 請求項1に記載の潤滑剤。 3. 潤滑剤が、ジエステル、フタレート、トリメリテート、ピロメリテート、ダ イマーアシッドエステル、ポリオール及びポリオレエートから選ばれた少なく とも1つのエステルを含むことを特徴とする、請求項1又は2に記載の潤滑剤 。 4. 潤滑剤が、約40重量%から約90重量%まで、好ましくは約50重量%か ら約80重量%までのエステルを含むことを特徴とする、請求項1−3の何れ か1つの項に記載の潤滑剤。 5. 鎖伝導、パーチクルボードプレス、テンターフレーム及びステンターフレー ム用潤滑剤として、請求項1ー4の何れか1つの項に記載の潤滑剤の使用。 6. 高温での潤滑剤の揮発度を減少させるために、エステルを含む潤滑剤中での アルキル置換ナフタレンの使用。[Claims] 1. A lubricant containing an alkyl-substituted naphthalene and an ester. 2. from about 10% to about 50%, preferably about 12% by weight of the lubricant;   Containing up to about 30% by weight of an alkyl-substituted naphthalene,   The lubricant according to claim 1. 3. If the lubricant is diester, phthalate, trimellitate, pyromellitate,   At least one selected from imer acid esters, polyols and polyoleates   The lubricant according to claim 1, further comprising one ester.   . 4. If the lubricant is from about 40% to about 90% by weight, preferably about 50% by weight.   4. The composition of any of claims 1-3, wherein the ester comprises up to about 80% by weight of an ester.   The lubricant according to any one of the above items. 5. Chain conduction, particle board press, tenter frame and stenter frame   Use of the lubricant according to any one of claims 1 to 4 as a lubricant for the system. 6. Reduce the volatility of lubricants at elevated temperatures by reducing the   Use of alkyl-substituted naphthalenes.
JP10505719A 1996-07-12 1997-07-10 Lubricants containing alkyl-substituted naphthalenes and esters Ceased JP2000514853A (en)

Applications Claiming Priority (3)

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US2169496P 1996-07-12 1996-07-12
US60/021,694 1996-07-12
PCT/GB1997/001857 WO1998002510A1 (en) 1996-07-12 1997-07-10 A lubricant comprising an alkyl-substituted naphthaline and an ester

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JP2000514853A true JP2000514853A (en) 2000-11-07
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Cited By (4)

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JP2005330328A (en) * 2004-05-18 2005-12-02 Osamu Ogata Method of improving oil performance
JP2017538840A (en) * 2014-12-17 2017-12-28 クリューバー リュブリケーション ミュンヘン ソシエタス ヨーロピア ウント コンパニー コマンディートゲゼルシャフトKlueber Lubrication Muenchen SE & Co.KG High temperature lubricants for the food industry
JP2017538838A (en) * 2014-12-17 2017-12-28 クリューバー リュブリケーション ミュンヘン ソシエタス ヨーロピア ウント コンパニー コマンディートゲゼルシャフトKlueber Lubrication Muenchen SE & Co.KG High temperature lubricant
WO2019189834A1 (en) * 2018-03-30 2019-10-03 出光興産株式会社 Lubricant composition

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US6436882B1 (en) 2001-06-29 2002-08-20 King Industries, Inc. Functional fluids
WO2007131891A1 (en) * 2006-05-15 2007-11-22 Shell Internationale Research Maatschappij B.V. Lubricating oil composition
DE202006019075U1 (en) * 2006-09-13 2007-04-12 Addinol Lube Oil Gmbh High temperature lubricant, useful in lubricating chains, comprises oil mixture comprising trimellitate ester, polyolester and complex ester, additive package, high pressure additives, antioxidants, metal-deactivator and wear reducer
CN106833825A (en) * 2016-12-08 2017-06-13 天长市天龙泵阀成套设备厂 The chain greasisng oil of greasy property can be improved
CN108865360A (en) * 2018-07-26 2018-11-23 郑州市欧普士科技有限公司 A kind of environment-friendly type synthesizing ester high-temperature chain oil and preparation method thereof

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JPH02286792A (en) * 1989-04-28 1990-11-26 Nippon Oil Co Ltd Lubricating oil composition
DK0496486T3 (en) * 1991-01-11 1994-03-28 Mobil Oil Corp Lubricant Compositions
US5236610A (en) * 1992-02-03 1993-08-17 The United States Of America As Represented By The Secretary Of The Commerce Stable high temperature liquid lubricant blends and antioxidant additives for use therewith

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005330328A (en) * 2004-05-18 2005-12-02 Osamu Ogata Method of improving oil performance
JP2017538840A (en) * 2014-12-17 2017-12-28 クリューバー リュブリケーション ミュンヘン ソシエタス ヨーロピア ウント コンパニー コマンディートゲゼルシャフトKlueber Lubrication Muenchen SE & Co.KG High temperature lubricants for the food industry
JP2017538838A (en) * 2014-12-17 2017-12-28 クリューバー リュブリケーション ミュンヘン ソシエタス ヨーロピア ウント コンパニー コマンディートゲゼルシャフトKlueber Lubrication Muenchen SE & Co.KG High temperature lubricant
WO2019189834A1 (en) * 2018-03-30 2019-10-03 出光興産株式会社 Lubricant composition
JPWO2019189834A1 (en) * 2018-03-30 2021-04-15 出光興産株式会社 Lubricating oil composition

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KR20000023606A (en) 2000-04-25
CN1230212A (en) 1999-09-29
AU3454397A (en) 1998-02-09
NO990104D0 (en) 1999-01-11
TR199900054T2 (en) 1999-03-22
NO990104L (en) 1999-01-11
BR9710296A (en) 1999-08-17
CZ6799A3 (en) 1999-08-11
EP0912663A1 (en) 1999-05-06
CA2260046A1 (en) 1998-01-22
PL331096A1 (en) 1999-06-21
WO1998002510A1 (en) 1998-01-22

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