JPH0320394A - Turbine oil composition - Google Patents
Turbine oil compositionInfo
- Publication number
- JPH0320394A JPH0320394A JP15410089A JP15410089A JPH0320394A JP H0320394 A JPH0320394 A JP H0320394A JP 15410089 A JP15410089 A JP 15410089A JP 15410089 A JP15410089 A JP 15410089A JP H0320394 A JPH0320394 A JP H0320394A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- turbine
- antioxidant
- turbine oil
- oxidation stability
- 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.)
- Granted
Links
- 239000010723 turbine oil Substances 0.000 title claims abstract description 30
- 239000000203 mixture Substances 0.000 title claims description 11
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 14
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 14
- 239000002199 base oil Substances 0.000 claims abstract description 14
- 239000002480 mineral oil Substances 0.000 claims abstract description 7
- 235000010446 mineral oil Nutrition 0.000 claims abstract description 7
- 125000003118 aryl group Chemical group 0.000 claims description 8
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 7
- 239000003112 inhibitor Substances 0.000 claims description 5
- 230000003647 oxidation Effects 0.000 abstract description 21
- 238000007254 oxidation reaction Methods 0.000 abstract description 21
- 239000003921 oil Substances 0.000 abstract description 14
- 239000002253 acid Substances 0.000 abstract description 7
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 238000013112 stability test Methods 0.000 description 11
- 239000000654 additive Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical group CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- -1 alkenyl succinic acids Chemical class 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010248 power generation Methods 0.000 description 4
- 238000001179 sorption measurement Methods 0.000 description 4
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 101000823778 Homo sapiens Y-box-binding protein 2 Proteins 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000004811 liquid chromatography Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- HXDOZKJGKXYMEW-UHFFFAOYSA-N 4-ethylphenol Chemical compound CCC1=CC=C(O)C=C1 HXDOZKJGKXYMEW-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 235000011044 succinic acid Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 235000005956 Cosmos caudatus Nutrition 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000003254 anti-foaming effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- CMCJNODIWQEOAI-UHFFFAOYSA-N bis(2-butoxyethyl)phthalate Chemical compound CCCCOCCOC(=O)C1=CC=CC=C1C(=O)OCCOCCCC CMCJNODIWQEOAI-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000010725 compressor oil Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010720 hydraulic oil Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000010721 machine oil Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 125000005461 organic phosphorous group Chemical group 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Lubricants (AREA)
Abstract
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は改良されたタービン油題戒物に関する。[Detailed description of the invention] (Industrial application field) The present invention relates to an improved turbine oil remedy.
さらに詳しくは使用期間が著しく長く、しかも酸化安定
性及び色安定性に優れるタービン油組戒物に関する。More specifically, it relates to a turbine oil composition that has a significantly long period of use and has excellent oxidation stability and color stability.
(従来技術)
タービン油は元来5〜20年という長期間にわたって無
交換で使用される潤滑油であるので高い酸化安定性、抗
乳化性、消I泡性、さび止め性、耐腐食性等各種の性能
が要求されている。これらのの場合、精製された鉱油な
基油にし各種の添加剤を添加することが必要である。し
かし、近年の超大型蒸気タービンの開発に伴なって,従
来以上の過酷な使用条件に耐えるタービン油の必要性が
高1っており、特に高度の酸化安定性が要求されるよう
になってきている。従来はJIS K 2514に規定
されているタービン油酸化安定度試験で1000時間経
過後の酸価が1.oqKOH/P以下であれば良いとさ
れているが、最近の情勢では2000および2500時
間後に酸価が1.09KOH/?以下であるようなター
ビン油が一般的になってきた。(Prior art) Turbine oil is originally a lubricating oil that is used for a long period of 5 to 20 years without being replaced, so it has high oxidation stability, demulsifying property, anti-foaming property, rust prevention property, corrosion resistance, etc. Various types of performance are required. In these cases, it is necessary to use a refined mineral base oil and add various additives. However, with the development of ultra-large steam turbines in recent years, there is an increasing need for turbine oils that can withstand even harsher operating conditions than before, and a particularly high level of oxidation stability is now required. ing. Conventionally, in the turbine oil oxidation stability test specified in JIS K 2514, the acid value after 1000 hours was 1. It is said that it is good if the acid value is less than oqKOH/P, but the current situation is that the acid value is 1.09KOH/P after 2000 and 2500 hours? Turbine oils that are:
特に発電用タービン油においてはこれらに対応するため
、通常極めて高度に精製した基油に酸化防止剤として2
,6−ジターシャリープチル−4一メチルフェノール(
以下DBPCと略す。)を配合したものが使用されてい
る。さらに特公昭59−25834にはこれらにトリー
p−}リルフtス7エートを添加したものが開示されて
いる。Particularly in the case of turbine oil for power generation, in order to cope with these problems, antioxidants are usually added to extremely highly refined base oil.
, 6-ditertiarybutyl-4-methylphenol (
Hereinafter abbreviated as DBPC. ) is used. Furthermore, Japanese Patent Publication No. 59-25834 discloses a product in which tri-p-}lylph t-7ate is added to these.
(解決しようとする課題)
発電用タービンの潤滑油系においては、混入水分の除去
、油の外部リーク防止および油へ温大した冷却用水素を
鋭気するためオイルタンクが減圧下にさらされる場合が
あb、この場合、従来の酸化防止剤では短期間に補油し
なければならないという問題がある。又、通常タービン
油の補油あるいは更油の目安としてボンベ寿命(回転ボ
ンベ式酸化安定度試験( JIS K 2514 )結
果であb、タービン油の残存寿命の目安となる値。)が
50〜100分以上になるように管理されているため酸
化安定度試験で2, 0 0 0〜2, 5 0 0時
間のものでも、比較的早期に補油を必要とする場合があ
る。(Problem to be solved) In the lubricating oil system of power generation turbines, the oil tank is sometimes exposed to reduced pressure in order to remove mixed water, prevent oil from leaking to the outside, and release heated hydrogen for cooling into the oil. In this case, conventional antioxidants have the problem of having to be refueled in a short period of time. In addition, as a guide for bunkering or replacing turbine oil, the cylinder life (results from the rotating cylinder oxidation stability test (JIS K 2514) b, a value that is a guideline for the remaining life of the turbine oil) is 50 to 100. Even if the oxidation stability test is 2,000 to 2,500 hours, bunkering may be required relatively early.
このため、補油あるいは更油期間がさらに延長できるよ
うな優れた酸化安定性を有するタービン油であれば極め
て有効である。Therefore, a turbine oil with excellent oxidation stability that can further extend the bunkering or oil replacement period is extremely effective.
(問題を解決するための手段)
本発明は、上記課題を解決するため鋭意検討を重ねた結
果、ある種の選択された基油を用い、これに対し特定の
酸化防止剤を配合することによb驚〈べき程長い使用寿
命を示し、したがって補油あるいは更油の期間が従来に
比し約2倍延長できる優れた酸化安定性を有し、かつ色
安定性に優れたタービン油が得られることを見い出し、
本発明を完或するに至った。(Means for Solving the Problem) As a result of intensive studies to solve the above problems, the present invention uses a certain selected base oil and blends a specific antioxidant with it. A turbine oil with excellent oxidation stability and excellent color stability, which has a surprisingly long service life and can extend the period of relubrication or oil replacement by about twice that of conventional oils, has been obtained. find out what you can do,
The present invention has now been completed.
すなわち本発明は、芳香族含有量8%以下である鉱油を
基油としさび止め剤と酸化防止剤を含んでなう、当核酸
化防止剤が2,6−ジターシャリープチル−4−エチル
フェノールであることを特徴とするタービン油組成物に
存する。That is, the present invention uses mineral oil with an aromatic content of 8% or less as a base oil and contains a rust inhibitor and an antioxidant, and the nuclear antioxidant is 2,6-ditertiarybutyl-4-ethylphenol. A turbine oil composition characterized in that:
以下に本発明を詳細に説明する。The present invention will be explained in detail below.
本発明において使用されるタービン油の基油は、高度精
製鉱油を用いる。具体的には芳香族含有量が約8qb以
下、好ましくは約2〜5憾の鉱油を用いるのが適当であ
る。芳香族分が多過ぎると優れた酸化防止効果が得られ
ず、少なすぎるとさびが発生し易くなる。上記条件を満
たす鉱油を得る方法は任意に選ぶことができる。例えば
原油を常圧蒸留、減圧蒸留をした後溶剤脱ろうと溶剤精
製一酸白土処理、溶剤精製一水素精製、あるいは水素化
分解とを適宜組み合わせることによって該基油を傳るこ
とができ、場合によっては脱れき工程を経る必要がある
。The base oil of the turbine oil used in the present invention is highly refined mineral oil. Specifically, it is appropriate to use a mineral oil having an aromatic content of about 8 qb or less, preferably about 2 to 5 qb. If the aromatic content is too large, excellent antioxidant effects cannot be obtained, and if the aromatic content is too small, rust is likely to occur. A method for obtaining mineral oil that satisfies the above conditions can be arbitrarily selected. For example, the base oil can be obtained by subjecting crude oil to atmospheric distillation or vacuum distillation, followed by solvent dewaxing, solvent refining, monoacid clay treatment, solvent refining and hydrogen refining, or hydrocracking, as appropriate. It is necessary to go through a descaling process.
本発明で用いる基油は、以上のような処理を経て得られ
るが、実際には芳香族含有量が約8%以下、好筐しくは
約2〜5%であればよい。一般に潤滑油基油中には種々
の成分、例えば飽和炭化水素、芳香族炭化水素、さらに
微量成分として硫黄化合物、窒素化合物が含まれる。通
常、タービン油の基油のように比較的分子量の高い留分
中の組成は、個々の化合物を分析することは不可能で、
実用上は組成のタイプ分析を行うことにより組或を決定
している。タイプ分析の方法としては種々の方法がある
が液体クロマト分析を採用することが好1しく、この方
法によシ飽和炭化水素威分、芳香族炭化水素成分および
樹脂分に分別することができる。本発明における基油は
この液体クロマト分析によう芳香族含有量が約8%以下
、好筐し〈は約2〜5%であることが必要である。液体
クロマト分析は次のように行われる。The base oil used in the present invention is obtained through the above-described treatment, but in reality, the aromatic content may be about 8% or less, preferably about 2 to 5%. Generally, lubricating base oils contain various components such as saturated hydrocarbons, aromatic hydrocarbons, and trace components such as sulfur compounds and nitrogen compounds. Normally, it is impossible to analyze the composition of individual compounds in fractions with relatively high molecular weights, such as the base oil of turbine oil.
In practice, composition is determined by performing composition type analysis. Although there are various methods for type analysis, it is preferable to employ liquid chromatography, which allows separation into saturated hydrocarbon components, aromatic hydrocarbon components, and resin components. The base oil used in the present invention must have an aromatic content of about 8% or less, preferably about 2 to 5%, as determined by liquid chromatography analysis. Liquid chromatography analysis is performed as follows.
秋着管に詰めた活性シリカゲルを予めn−へブタンで湿
しておき、賦料油を秤量し、試料油と等量のn−へブタ
ンで希釈して吸着管に注入する。Activated silica gel packed in a fall tube is moistened in advance with n-hebutane, excipient oil is weighed out, diluted with n-hebutane in the same amount as the sample oil, and injected into the adsorption tube.
以後は規定量のn−へブタン、ペンゼyおよびメタノー
ルを順次加えて吸着管の下部に押し流す。Thereafter, specified amounts of n-hebutane, penzey, and methanol are sequentially added and flushed to the bottom of the adsorption tube.
シリカゲルに対する試料油および各溶剤の吸着力の差に
よう試料油は各炭化水素威分に分離して溶出する。吸着
管の下端から溶出した各炭化水素成分はその溶剤を蒸発
したのち秤量する。Due to the difference in the adsorption power of the sample oil and each solvent to the silica gel, the sample oil is separated into each hydrocarbon component and eluted. Each hydrocarbon component eluted from the lower end of the adsorption tube is weighed after its solvent has been evaporated.
芳香族炭化水素成分の割合(%)は次式から求められる
。The proportion (%) of the aromatic hydrocarbon component is determined from the following formula.
芳香族炭化水素成分の割合(%) =
ベンゼン溶出分×100
n−へブタン溶出分十ベンゼン溶出分十メタノール溶出
分?発明に用いる添加剤2,6ジターシャリープチル−
4−エチルフェノールは酸化防止剤であbC■,H,,
O(分子量:234、融点約43C以上)で示される淡
黄白色結晶である。Ratio of aromatic hydrocarbon components (%) = Benzene eluate x 100 n-hebutane eluate 10 benzene eluate 10 methanol eluate? Additive used in the invention 2,6 ditertiary butyl
4-Ethylphenol is an antioxidant bC■,H,,
It is a pale yellowish white crystal represented by O (molecular weight: 234, melting point about 43C or more).
一般にはパラエチルフェノールをブチル化した後精製し
て得られる。この添加剤の具体例としてはスワノックス
316(丸善石油化学製)、ヨシノックス250(吉富
製薬製)等を用いることができる。Generally, it is obtained by butylating para-ethylphenol and then purifying it. Specific examples of this additive include Swanox 316 (manufactured by Maruzen Petrochemical), Yoshinox 250 (manufactured by Yoshitomi Pharmaceutical), and the like.
添加量は好ましくは0.1〜1. 0 4であう,さら
に好喧しくは0.2〜0.94である。少なすぎると効
果がなく、多すぎても添加量に見合う効果は得られない
。The amount added is preferably 0.1 to 1. 0.4, more preferably 0.2 to 0.94. If it is too small, there will be no effect, and if it is too large, the effect commensurate with the amount added will not be obtained.
本発明に用いられるさび止め剤は、通常のものを用いる
ことができる。好1しくはアルケニルこはく酸あるいは
、その部分エステルを用いることができる。As the rust inhibitor used in the present invention, ordinary ones can be used. Preferably, alkenylsuccinic acid or a partial ester thereof can be used.
アルケニルこはく酸は次のような構造を有している。す
なわち、
R− CHCOOH
1
CH,COOH
ここでRは平均12〜20の炭素数をもつアルケニル基
で通常プロピレンやプデン類のオリゴマーを導入して合
成される。Alkenylsuccinic acid has the following structure. That is, R- CHCOOH 1 CH,COOH where R is an alkenyl group having an average of 12 to 20 carbon atoms, and is usually synthesized by introducing an oligomer of propylene or pudene.
一方、アルケエルこはく酸の部分エステルは、上配のア
ルケニルこは〈酸を原料とし、エチレンオキシド、プロ
ピレンオキシド等のアルキレンオキシドあるいはエチレ
ングリコール、ペンタエリスリトール等の多価アルコー
ルを反応させて部分エステル化したもので、好璽しくは
カルボキシル基の50係以下のエステル化率のものが適
切である。添加量は0.03〜1.Ol%、好1し〈は
0.03〜0.06.%である。少なすぎると効果がな
く、多過ぎると酸化防止効果の妨げとなる。その他のさ
び止め剤としてはスルホン酸塩、脂肪族アミン類、有機
亜りん酸およびシん酸エステル等がある。On the other hand, partial esters of alkenyl succinic acids are partially esterified by reacting the upper alkenyl succinic acids with alkylene oxides such as ethylene oxide and propylene oxide or polyhydric alcohols such as ethylene glycol and pentaerythritol. Preferably, the esterification rate of the carboxyl group is 50 or less. The amount added is 0.03 to 1. Ol%, preferably 1, is 0.03 to 0.06. %. If it is too small, there will be no effect, and if it is too large, the antioxidant effect will be hindered. Other rust inhibitors include sulfonates, aliphatic amines, organic phosphorous acids, and sic acid esters.
本発明のタービン油組成物はさび止め剤と酸化防止剤を
含んで々シ、当核酸化防止剤が2.6−ジターシャリー
プチル−4−エチルフェノール(以下DBEPと略す。The turbine oil composition of the present invention contains a rust inhibitor and an antioxidant, and the nuclear antioxidant is 2,6-ditertiarybutyl-4-ethylphenol (hereinafter abbreviated as DBEP).
)であるが、更に酸化安定性を低下させない添加剤を加
えることができる。例えば消泡剤としてポリアクリレー
ト系あるいはシリコン系添加剤を添加することができる
。さらに極圧剤としてトリクレジル7オス7エート等の
リン化合物、金属不活性化剤としてペンゾトリアゾール
誘導体等を用いることができる。又、DBPCとDBE
Pとの併用使用も可能である。), but further additives can be added that do not reduce the oxidative stability. For example, a polyacrylate or silicone additive can be added as an antifoaming agent. Further, a phosphorus compound such as tricresyl 7-mole 7-ate can be used as an extreme pressure agent, and a penzotriazole derivative or the like can be used as a metal deactivator. Also, DBPC and DBE
It is also possible to use it in combination with P.
本発明の主たる用途は発電用タービン油であるが、油圧
作動油、コンプレッサー油、軸受油、機械油への応用も
可能である。Although the main application of the present invention is turbine oil for power generation, it can also be applied to hydraulic oil, compressor oil, bearing oil, and machine oil.
(発明の効果)
本発明品は、タービン油酸化安定度試験において優れた
酸化安定性を示す。特に、酸化による劣化速度が従来の
ものに比して約1/2程度であう、したがって、発電用
タービン油の補油あるいは更油期間を著しく延長するこ
とが可能である。(Effects of the Invention) The product of the present invention exhibits excellent oxidation stability in a turbine oil oxidation stability test. In particular, the rate of deterioration due to oxidation is about 1/2 that of conventional oil, so it is possible to significantly extend the bunkering or replacement period for power generation turbine oil.
本発明のタービン油組成物中で用いられている酸化防止
剤は、従来用いられてきたDBPCのメチル基をエチル
基に変化させたものであるが、炭素原子1個の増加によ
り酸化安定性が2倍も改善されるということは全く予想
外の篤〈べき事実である。又、色劣化が少なく、極めて
優れた色安定性を示す。The antioxidant used in the turbine oil composition of the present invention is obtained by changing the methyl group of conventionally used DBPC to an ethyl group, but the oxidation stability is reduced due to the increase of one carbon atom. It is a completely unexpected and serious fact that the improvement is twice as great. In addition, there is little color deterioration and extremely excellent color stability is exhibited.
(実施例)
以下、実施例を挙げて本発明を具体的に説明するが、こ
れらによυ本発明が制約されるものではない。(Examples) Hereinafter, the present invention will be specifically explained with reference to Examples, but the present invention is not limited by these.
実施例1〜6、比較例1〜4
芳香族含有量を調整し・た基油に添加剤を添加して添加
タービン油を調製した。組成を第1表に示す。又、これ
ら調製した各試料について各種試験を実施し評価した。Examples 1 to 6, Comparative Examples 1 to 4 Additives were added to base oils whose aromatic content had been adjusted to prepare additive turbine oils. The composition is shown in Table 1. In addition, various tests were conducted and evaluated for each of these prepared samples.
〈酸化安定度試験{!}〉
JIS K 2514に準拠し、タービン油酸化安定度
試験を実施した。得られた結果を第1表に示す。<Oxidation stability test {! }> A turbine oil oxidation stability test was conducted in accordance with JIS K 2514. The results obtained are shown in Table 1.
第1表の結果から明らかなように本発明品であるタービ
ン油はいずれもタービン油酸化安定度試でなく、鋼板腐
食性が低、〈Jさび止め性、色相、消泡性、抗乳化性等
についても極めて優れた性能を有するものであることが
分った。As is clear from the results in Table 1, none of the turbine oils of the present invention were tested for turbine oil oxidation stability, and had low corrosion resistance to steel sheets. It was also found that it has extremely excellent performance.
〈酸化安定度試験(2)〉
タービン油酸化安定度試験( JIS K 2514
)の途中経過時間である1,000時間、1,500時
間において試料(50P)を採取し、その試料について
回転ポンペ式酸化安定度試験(JIS K 2514)
を行い、ボンベ寿命を求め残存寿命の指標とした。<Oxidation stability test (2)> Turbine oil oxidation stability test (JIS K 2514
) Samples (50P) were collected at 1,000 hours and 1,500 hours, and the samples were subjected to a rotary pump oxidation stability test (JIS K 2514).
The cylinder life was determined and used as an indicator of remaining life.
得られた結果を第2表に示す。The results obtained are shown in Table 2.
第2表の結果から明らかなように本発明品は、タービン
油酸化安定度試験の1, 0 0 0時間、1,500
時間においてもボンベ寿命は高く、残存寿命も長い。こ
のため、ボンベ寿命の低下率から推定すると実施例は比
較例に比べ約2倍の補油あるいは更油期間の延長が期待
出来る。As is clear from the results in Table 2, the product of the present invention was tested for turbine oil oxidation stability for 1,000 hours and 1,500 hours.
The cylinder life is high in terms of time, and the remaining life is also long. Therefore, when estimated from the rate of decrease in cylinder life, the Example can be expected to extend the refueling or oil change period approximately twice as much as the Comparative Example.
〈色安定度賦験〉
温度120C、試料量50d、触媒として鉄板および銅
板(50X20X1(m))の両者の存在下あるいは無
触媒下、1週間の試験時間における色の経時変化をみた
。<Color Stability Test> Changes in color over time were observed at a temperature of 120 C, a sample amount of 50 d, in the presence of both an iron plate and a copper plate (50 x 20 x 1 (m)) as catalysts, or in the absence of a catalyst, over a test period of one week.
得られた結果を第l図に示した。図から明らかなように
本発明品は色劣化が少なく、極めて優れた色安定性を示
した。The results obtained are shown in Figure 1. As is clear from the figure, the product of the present invention exhibited little color deterioration and exhibited extremely excellent color stability.
第1図は色安定度試験の結果を示す。
横軸は時間、縦軸は色(ASTM)を示す。数字は、1
,2・・・実施例1、3・・・実施例5、4・・・比較
例l、5・・・比較例3である。実線は触媒存在下、破
線は無触媒下である。
出 願人 コスモ石油株式会社
東北電力株式会社Figure 1 shows the results of the color stability test. The horizontal axis represents time, and the vertical axis represents color (ASTM). The number is 1
, 2...Example 1, 3...Example 5, 4...Comparative example 1, 5...Comparative example 3. The solid line is in the presence of a catalyst, and the broken line is in the absence of a catalyst. Applicant Cosmo Oil Co., Ltd. Tohoku Electric Power Co., Ltd.
Claims (1)
め剤と酸化防止剤を含んでなり、当該酸化防止剤が2,
6−ジターシャリーブチル−4−エチルフェノールであ
ることを特徴とするタービン油組成物。1. Mineral oil with an aromatic content of 8% or less is used as a base oil and contains a rust inhibitor and an antioxidant, and the antioxidant is 2.
A turbine oil composition characterized in that it is 6-ditertiarybutyl-4-ethylphenol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1154100A JPH0742468B2 (en) | 1989-06-16 | 1989-06-16 | Turbine oil composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1154100A JPH0742468B2 (en) | 1989-06-16 | 1989-06-16 | Turbine oil composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0320394A true JPH0320394A (en) | 1991-01-29 |
JPH0742468B2 JPH0742468B2 (en) | 1995-05-10 |
Family
ID=15576919
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1154100A Expired - Lifetime JPH0742468B2 (en) | 1989-06-16 | 1989-06-16 | Turbine oil composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0742468B2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5254706A (en) * | 1975-10-31 | 1977-05-04 | Nippon Oil Co Ltd | Improved turbine oil composition |
JPS62270697A (en) * | 1986-03-22 | 1987-11-25 | チバ−ガイギ− アクチエンゲゼルシヤフト | Lubricant composition |
-
1989
- 1989-06-16 JP JP1154100A patent/JPH0742468B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5254706A (en) * | 1975-10-31 | 1977-05-04 | Nippon Oil Co Ltd | Improved turbine oil composition |
JPS62270697A (en) * | 1986-03-22 | 1987-11-25 | チバ−ガイギ− アクチエンゲゼルシヤフト | Lubricant composition |
Also Published As
Publication number | Publication date |
---|---|
JPH0742468B2 (en) | 1995-05-10 |
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