JPH05502262A - Low volatility solvent for active substances containing aromatic components - Google Patents

Low volatility solvent for active substances containing aromatic components

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Publication number
JPH05502262A
JPH05502262A JP91502392A JP50239291A JPH05502262A JP H05502262 A JPH05502262 A JP H05502262A JP 91502392 A JP91502392 A JP 91502392A JP 50239291 A JP50239291 A JP 50239291A JP H05502262 A JPH05502262 A JP H05502262A
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JP
Japan
Prior art keywords
benzoic acid
carbon atoms
active substances
oil
low volatility
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
JP91502392A
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Japanese (ja)
Inventor
シュミット、カール
シュテバー、ヨーゼフ
ヴュースト、ラインホルト
ゴーデ、ペーター
Original Assignee
ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン
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Application filed by ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン filed Critical ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン
Publication of JPH05502262A publication Critical patent/JPH05502262A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるため要約のデータは記録されません。 (57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 芳香族成分を含む活性物質の為の低揮発性溶剤本発明は、油の、例えば油圧動力 伝動装置用の油圧流体としての使用における改良に関する。[Detailed description of the invention] Low volatility solvent for active substances containing aromatic components This invention relates to improvements in its use as a hydraulic fluid for power transmissions.

油が、例えば避けがたい漏出口から周囲に漏れる可能性があるものに油圧油を使 用する場合、環境に温和なエステル油、特に菜種油および/または大豆油を基剤 油として含む油圧油の需要が多くなりつつある。問題となる種類の典型的実例は 、林業および農業で使用する機械および工具、掘削機等である。ウォーター・ハ ザード指数(Water Hazard C1assification)が0 である油圧油の使用が、そ油圧油とは対照的に、相応するエステルを基剤とする 油は環境保護の目的にかなうものである。Hydraulic fluids are used in applications where oil may leak into the surrounding environment, e.g. through unavoidable leaks. When used, environmentally benign ester oils, especially rapeseed and/or soybean oil based Demand for hydraulic oil containing oil is increasing. A typical example of the kind of problem is , machinery and tools used in forestry and agriculture, excavators, etc. water ha Water Hazard C1 assignment is 0 The use of hydraulic fluids that are, in contrast to hydraulic fluids, based on corresponding esters The oil serves environmental protection purposes.

しかし、実用に適したエステル油、例えば粘性の低い菜種油およ・不飽和脂肪酸 系を基剤とするエステル油は、やや高い作業温度、例えば50〜80℃において さえ、速やかに粘度が上かる傾向にある。この原因は、ここで問題としている油 類のエステルを形成して、 いる酸のオレフィン性二重結合が、環境酸素の影響 下に、最終的には粘度の上昇につながる反応へと進みゃすいことにある。原則的 に、油圧油のこのような望ましくない粘度の上昇は、酸化防止剤の添加1 に= J″〈あ6程度防止可能tJ6が・1がL′:tl、ら0場合・満足0得られる 程度まで、特に長期間にわたって効果を持続させることはI 困難1あ3が知ら 0″い6.、:、:”r問題2じい6種類Om2チル油の作業寿命を延ばす為に は、多(の場合、一定期間後により多くの酸化防止剤、腐食防止剤等を添加する ことが必要となる。However, ester oils suitable for practical use, such as rapeseed oil with low viscosity and unsaturated fatty acids, Ester oils based on the However, the viscosity tends to increase rapidly. The cause of this is the oil in question here. The olefinic double bond of the acid forms esters of The downside is that it is easy to proceed to a reaction that ultimately leads to an increase in viscosity. principle This undesirable increase in the viscosity of the hydraulic oil is caused by the addition of antioxidants. J″〈A 6 degree can be prevented if tJ6 is ・1 is L′: tl, ra 0 ・Satisfaction 0 can be obtained It is difficult to maintain the effect to a certain extent, especially over a long period of time. 0"6.,:,:"rProblem 2 - 6 types of Om2To extend the working life of chill oil In the case of multi-oxidation, more antioxidants, corrosion inhibitors, etc. are added after a certain period of time. This is necessary.

酸化防止剤、腐食防止剤等の類いの添加が必要な助剤は、しばしば、常にではな いにせよ、少なくとも部分的に芳香族成分を含む化合物である。望ましくない環 境酸素の攻撃に対抗する適切な助剤または活性物質には、とりわけフェノール構 造体および/またはヒドロ牛/ン誘導体が多くミられる。例えば、本出願人によ る先の特許出願P3927155.2 [D8826“エンバイロメントーフレ ンドリー・ベース・オイル・フォー・ザ・フォーミュレーシゴン・オブ・ヒドラ ウリツク・オイルズ(Environment−friendly baseo il for the [’ormulation of hydraulic  oils) ’]では、油圧油の配合の為の、以下の成分を含む対応する天然 基剤性は、使用時の活性および/または低温安定性において改善がみられると記 載している a)油止成分として精製菜種油および/または大豆油b)メトキシフェノール、 エトキシフェノール、ブチルヒドロキシアニンール、ブチルヒドロキシトルエン 、メトキシヒドロ十ノペエトキ/ヒドロキシン、第三ブチルヒドロキノンおよび /またはトコフェロールから成る群から選択した抗酸化剤を混合物全体に対して 0. 5〜5重量%、および所望によりC)トリメチロールエタン、トリメチロ ールプロパンおよび/またはネオペンチルグリコールの、以下の項に属するモノ カルボン酸とのエステル。Auxiliary agents such as antioxidants, corrosion inhibitors, etc. that require addition are often, but not always, In any case, it is a compound that contains at least partially aromatic components. undesirable ring Suitable auxiliaries or active substances to counteract the attack of ambient oxygen include, inter alia, phenolic compounds. A large number of synthetic and/or hydrochloric acid derivatives are found. For example, the applicant Previous patent application P3927155.2 [D8826 “Environment undry base oil for the formula of hydra Uritsuk Oils (Environment-friendly baseo) il for the [’ormulation of hydrolic  oils) ] for the formulation of hydraulic oils, we offer corresponding natural products containing the following ingredients: Regarding base properties, it is reported that there is improvement in activity during use and/or low temperature stability. It is listed a) Refined rapeseed oil and/or soybean oil as oil-stopping ingredients b) Methoxyphenol, Ethoxyphenol, butylated hydroxyanine, butylated hydroxytoluene , methoxyhydrodecanopeethoxy/hydroxyne, tert-butylhydroquinone and / or an antioxidant selected from the group consisting of tocopherols to the entire mixture. 0. 5 to 5% by weight, and optionally C) trimethylolethane, trimethyl Polypropane and/or neopentyl glycol belonging to the following categories: Esters with carboxylic acids.

CI)飽和C5−toモ/カルボン酸および/またはC2)菜種油、大豆油およ び/または工業用オレイン酸を基材とする脂肪酸 エステル成分C)は、油止成分a)と実質上同量で存在する。CI) saturated C5-tomo/carboxylic acids and/or C2) rapeseed oil, soybean oil and and/or industrial oleic acid-based fatty acids Ester component C) is present in substantially the same amount as oilstop component a).

芳香族成分を主成分とする抗酸化剤のみを成分b)として使用する。これらのよ うな環境に温和な基剤油を実際に使用する為には、安定剤が好ましくは高a度で 溶解している活性物質a厚液を製造することがより望ましいということが判って いる。これらの活性物質濃厚液を後から添加することによって、油圧油の寿命を 効果的に延ばすことができる。しがし、溶剤の選択に多少問題がある。前述の種 類の活性物質a厚液は、低揮発性であり、常温で流動性がありがつ、使用する活 性物質の芳香族基本構造と相溶性が高く活性物質を必要な高濃度に確実に溶解す る溶剤を必要とする。部分的に芳香族基本構造を持つ溶剤もこの条件を満たすも のである。これらの基本的考察からすると、現在広く使用されているジブチルフ タレート(DBP)が、必要な活性物質濃厚液の製造に適した代表的溶剤である 。Only antioxidants based on aromatic components are used as component b). these For practical use of mild base oils in such environments, stabilizers are preferably used at high a. It has been found that it is more desirable to produce a thick solution of the active substance in solution. There is. The life of hydraulic oil can be extended by adding these active substance concentrates later. can be effectively extended. However, there is some problem with the selection of solvent. the aforementioned species Thick liquids of active substances of type A have low volatility and are fluid at room temperature, depending on the active substance used. It has high compatibility with the aromatic basic structure of the active substance and can reliably dissolve the active substance at the required high concentration. Requires a suitable solvent. Solvents with a partially aromatic basic structure also satisfy this condition. It is. Based on these basic considerations, the currently widely used dibutyl Talate (DBP) is a typical solvent suitable for producing the required active substance concentrates. .

しかし、最近ではDBPの無制限の使用に対する生態学的および毒物学的論議が 報じられている。これが本発明の出発点である。However, recently ecological and toxicological arguments against the unrestricted use of DBPs have emerged. It has been reported. This is the starting point of the invention.

本発明が解決しようとする問題は、環境に温和な油相、例えば上記において引用 した出願人による先の特許出願に記載のエステル油のような、既知の種類の油相 の使用の為に、少なくとも部分的に芳香族分子構造を持ち、環境的適合性によっ て特徴付けられる、前述の種類の助剤を提供することである。とりわけ本発明は 、上記の・種類の抗酸化剤および/または腐食防止剤を、それ自身ウォーター・ ハザード指数が0である溶剤中に溶解している濃厚液の状態にし、同時に常温で 流動性のある高濃縮液の製造を可能にし、かつ特別な作業もなくエステル基剤油 圧油と安全に混和させることから成る。The problem that the present invention seeks to solve is to provide an environmentally benign oil phase, e.g. oil phases of known types, such as the ester oils described in earlier patent applications filed by the same applicant. have an at least partially aromatic molecular structure and are environmentally compatible. The object of the present invention is to provide an auxiliary agent of the above-mentioned type, which is characterized as follows. In particular, the present invention , antioxidants and/or corrosion inhibitors of the types mentioned above can be added to the water themselves. Make it into a concentrated liquid dissolved in a solvent with a hazard index of 0, and at the same time at room temperature. Ester base oil that enables the production of highly fluid concentrated liquids without any special work. It consists of being safely miscible with pressure oil.

本発明が解決すべき問題は、環境的適合性が高い低揮発性溶剤として選択した安 息香酸ジエステルの使用によって技術的に解決される。The problem to be solved by the present invention is to select a safe solvent with high environmental compatibility and low volatility. Technically solved by the use of zoic acid diesters.

従って本発明は、環境的適合性の高い脂肪および/または油、とりわけエステル を基剤とする油圧油において使用する際に、少なくとも部分的に芳香族分子構造 を持つ活性物質、例えば抗酸化剤および/または腐食防止剤の為の、低揮発性環 境温和性溶剤としての、選択した、常温で流動性のある、少なくとも4の炭素原 子を含む直鎖および/または分枝状脂肪族ジオールの安息香酸ジエステルの使用 に関する。The invention therefore provides environmentally compatible fats and/or oils, especially esters. When used in hydraulic oils based on low volatility rings for active substances such as antioxidants and/or corrosion inhibitors with At least four selected carbon atoms, which are fluid at room temperature, as environment-friendly solvents. Use of benzoic acid diesters of linear and/or branched aliphatic diols containing children Regarding.

別の態様において、本発明は、常温で流動性があり、少なくとも4の炭素原子を 含む直鎖および/または分枝状脂肪族ジオールの安息香酸ジエステルが溶剤とし て存在していることを特徴とする、少なくとも部分的に芳香族基本構造を持つ抗 酸化剤および/または腐食防止剤等の活性物質を含み、常温で流動性のある低揮 発性溶剤を基剤とする添加剤に関する。In another embodiment, the present invention provides a method that is fluid at room temperature and contains at least 4 carbon atoms. benzoic acid diesters of linear and/or branched aliphatic diols containing Antibiotics having an at least partially aromatic basic structure characterized by the presence of Contains active substances such as oxidizing agents and/or corrosion inhibitors, and is free-flowing at room temperature. It relates to additives based on emissive solvents.

本発明に従った好ましい低揮発性溶剤は、流動点が0℃以下、好ましくは一10 ℃以下であって、同時に引火点が150℃より低くない、好ましくは200°C 以上である、安息香酸/ジオールのジエステルである。このような特性を持つ安 息香酸ジエステルは、特にジオールの雨水酸基の間に直鎖状に並んだ4〜9の炭 素原子を含む、とりわけ5〜7の炭素原子を含むジオールまたはエステルのジオ ール部分から誘導する°。ジオール間のこの直鎖は置換されていなくてもよいし 、また好ましくは多くとも3までの炭素原子を含む低級アルキル基による置換に よって1回以上分枝していてもよい。7オ一ル部分に多くとも10の炭素原子を 含む、ジオールの安息香酸ジエステルか特に適している。Preferred low volatility solvents according to the invention have pour points below 0°C, preferably -10°C. ℃ or less, and at the same time the flash point is not lower than 150℃, preferably 200℃ The above is a diester of benzoic acid/diol. Safety products with these characteristics Zozoic acid diesters are particularly characterized by 4 to 9 carbon atoms arranged in a linear chain between the hydroxyl groups of diols. Diols or esters containing elementary atoms, especially containing 5 to 7 carbon atoms ° Guide from the core part. This straight chain between diols may be unsubstituted or , also preferably substituted with lower alkyl groups containing up to 3 carbon atoms. Therefore, it may be branched one or more times. At most 10 carbon atoms in the 7-ol moiety Particularly suitable are benzoic acid diesters of diols, including.

上記の種類の安息香酸ジエステルは、それらの性状を総合すると、文頭に記載し た特性条件を満足している。この種類のエステルは芳香族分子部分を持つので、 多量の芳香族活性物質を添加剤中に溶解させることができる。従って、選択した 溶剤における活性物質含量の設定は、通例5〜約50重量%、好ましくは約40 重量%まて可能である。安息香酸エステル自身は環境に温和であり、特にウォー ター・ハザード指数はOである。これらは例えば上記のエステル油を基剤とする 油圧油に対して容易に導入でき、均一に混和することができる。The above types of benzoic acid diesters can be summarized as described at the beginning of the text. It satisfies the specified characteristic conditions. This type of ester has an aromatic molecular moiety, so Large amounts of aromatic active substances can be dissolved in the additive. Therefore, selected The setting of the active substance content in the solvent is usually from 5 to about 50% by weight, preferably about 40%. % by weight is also possible. Benzoic acid esters themselves are environmentally benign, especially when it comes to water. The tar hazard index is O. These are based on the ester oils mentioned above, for example. It can be easily introduced into hydraulic oil and can be mixed uniformly.

本発明による添加剤を介して導入するに好ましい活性物質は、メトキンフェノー ル、エトキシフェノール、ブチルヒドロキシアニソール、プチルヒドロキシトル エン、メトキシヒドロキノン、エトキンヒドロキノン、第三ブチルヒドロキノン および/またはトコフェノールから成る群から選択した抗酸化剤である。他の典 型的活性物質も添加剤濃厚液に加えることができる。これらの他の添加剤の例は 高圧添加剤、摩耗防止添加剤および/または流動点降下剤である。Preferred active substances to be introduced via the additive according to the invention are metquinphenol. , ethoxyphenol, butylated hydroxyanisole, butylated hydroxytolu Ene, methoxyhydroquinone, ethquinhydroquinone, tert-butylhydroquinone and/or an antioxidant selected from the group consisting of tocophenols. other texts Type active substances can also be added to the additive concentrate. Examples of these other additives are High pressure additives, anti-wear additives and/or pour point depressants.

油圧油の更なる個々の成分については、関連の先行技術文献、特(こ“ウルマン ズ・エンツイクロペディー・デア・テヒニシエン・ヘミ−(U llmanns  E nzyklopMdie der technischen Chemi e)”、第4版[フェアラーク・ヘミ−(Verlag Chemie) 、ヴ アインノλイム(Weinheim)] 、第13巻、85頁以降参照、ヒドラ ウリクフリュスイヒカイテン(Hydraulikflussigkeiten )およびディーター・クラマン(D 1eter K lamann) “シュ ミーアシニド・ノフエ・ラント・フェアヴアンテ・プロドウクチ、ヘアシュテル ング、アイゲンシャフテン、アンウ゛エンドウング(S chmierstof fe und vervandteProdukte、Herstellung 、Eigenschaften、Anwendung)” 、[フエアラーク・ ヘミ−(Verlag Chemie)、つ゛アインノ飄イム(Weinhei m)コ1982.147/148頁−11.9、ヒドラウリコエーレ(Hydr aulik61e)において見られる。Further information on the individual components of hydraulic fluids can be found in the relevant prior art literature, in particular Ullmanns E zyklop Mdie der technischen Chemi e)”, 4th edition [Verlag Chemie, V. Weinheim], Volume 13, page 85 et seq., Hydra Hydraulikflussigkeiten (Hydraulikflussigkeiten) ) and Dieter Klamann Measinide nohue rant fairvante prodoukci, Herster. Schmierstof fe und vervandteProdukte, Herstellung , Eigenschaften, Anwendung) Verlag Chemie, Weinhei m) Ko1982.147/148 p.-11.9, Hydr. aulik61e).

本発明のとりわけ1つの態様において、安息香酸ジエステルはポリ−α−オレフ ィンとの混合物にし、溶剤相として使用する。この関連においては、ポリ−α− オレフィンは、中程度の鎖長のα−オレフィンの低重合体である。安息香酸ジオ ールジエステルの流動性条件を満たす低重合体は特に適している。単量体分子中 に6〜12の炭素原子を含むα−オレフィンの低重合体が好ましく、Ctoα− オレフィンの低重合体が特に好ましい。低重合体はまた、例えば2〜6個のα− オレフィンから形成する。安息香酸ジエステルはポリ−α−オレフィンとの混合 比を広くとることができ、適当な2成分の量比は約95:5〜5:95、好まし くは約70 : 30〜30:0.1%酸化スズの存在下において、ペンタン− 1,5−ジオール856gを安息香酸1832gによって200’C7時間エス テル化した。無色透明の油が得られ、その特性数値は以下のとおりであった・酸 価0. 3、水酸価29、ケン化価350゜この油の引火点は、ドイツ工業規格 (DIN)ISO2595によると224℃、流動点はドイツ工業規格l5O3 016によると一33℃および曇点はドイツ工業規格Is○3015によると一 12℃であった。In one particular embodiment of the invention, the benzoic acid diester is a poly-alpha-olefin. Mixture with fin and use as solvent phase. In this context, poly-α- Olefins are oligomers of medium chain length α-olefins. benzoic acid geo Low polymers that meet the flowability requirements of diesters are particularly suitable. in monomer molecules Ctoα-olefin oligomers containing 6 to 12 carbon atoms are preferred; Particularly preferred are oligomers of olefins. Low polymers may also contain e.g. 2 to 6 α- Formed from olefins. Benzoic acid diester mixed with poly-α-olefin The ratio can be set over a wide range, and the appropriate quantitative ratio of the two components is about 95:5 to 5:95, preferably 70: 30-30: In the presence of 0.1% tin oxide, pentane- 856 g of 1,5-diol was treated with 1832 g of benzoic acid at 200'C for 7 hours. It became a tell. A colorless and transparent oil was obtained, and its characteristic values were as follows: Value 0. 3. Hydroxy value: 29, saponification value: 350° The flash point of this oil is according to German industrial standards. (DIN) According to ISO2595, 224℃, pour point is German Industrial Standard 15O3 According to the German Industrial Standard Is○3015, the cloud point is -33℃ according to 016. The temperature was 12°C.

虫斡亘ユ ネオペンチルグリコール159g、)リメチロールプロノ<ン136gおよび安 息香酸366gを実施例1と同様に反応させエステル化した。無色の油が得られ 、約3日後に結晶化した。Wataru Mushihiro Neopentyl glycol 159g, )limethylolpronone 136g and 366 g of zozoic acid was reacted and esterified in the same manner as in Example 1. A colorless oil is obtained. , crystallized after about 3 days.

比較例2 安息香酸183gおよびプロパン−1,2−ジオール76gを実施例1と同様に 反応させエステル化した。結晶性の生成物が得られた。Comparative example 2 183 g of benzoic acid and 76 g of propane-1,2-diol were added in the same manner as in Example 1. The mixture was reacted and esterified. A crystalline product was obtained.

実施例2 ブチルヒドロキシアニソール30gを、実施例1で得られたエステル70gに6 0°Cにおいて溶解した。この混合物は一10’Cにおいて3週間以上液体状態 を保った。Example 2 Add 30 g of butylhydroxyanisole to 70 g of the ester obtained in Example 1. Dissolved at 0°C. This mixture remains in a liquid state for more than 3 weeks at -10'C. was maintained.

虫蝮圓l アンヒドロトリメリド酸342g、オクタツール323gおよびデカノール48 5gを実施例1と同様に反応させエステル化した。Insect insect circle 342 g of anhydrotrimellidic acid, 323 g of octatool and 48 g of decanol 5 g was reacted and esterified in the same manner as in Example 1.

無色の油が得られ、その特性数値は以下のとおりであった。酸価0.5、水酸価 2、ケン化価285゜この油の流動点はドイツ工業規格I 5O3016による と一42℃であり、引火点はドイツ工業規格l5O2595によると280℃で あった。A colorless oil was obtained, the characteristic values of which were as follows. Acid value 0.5, hydroxyl value 2. Saponification value: 285° The pour point of this oil is according to German Industrial Standard I 5O3016. According to the German Industrial Standard 15O2595, the flash point is 280°C. there were.

実施例2と同様に、ブチルヒドロキシアニソール30gを、比較例3で得られた エステル70gに60″Cにおいて溶解した。ブチルヒドロキシアニソールは混 合物から析出した。Similarly to Example 2, 30 g of butylhydroxyanisole obtained in Comparative Example 3 was Dissolved in 70g of ester at 60"C. Butylhydroxyanisole was mixed. It was precipitated from the compound.

要約書 環境的適合性の高い脂肪および/または油、とりわけエステルを基材とする油圧 油において使用する際に、少なくとも部分的に芳香族基本構造を持つ活性物質、 例えば抗酸化剤および/または腐食防止剤の為の、低揮発性環境1和性溶剤とし ての、選択した、常温で流動性がある、少なくとも4の炭素原子を持つ直鎖およ び/または分枝状脂肪族ジオールの安息香酸ジエステルの使用を開示する。abstract Hydraulics based on environmentally compatible fats and/or oils, especially esters active substances having an at least partially aromatic basic structure when used in oils; As a low volatility environmentally compatible solvent, e.g. for antioxidants and/or corrosion inhibitors. straight-chain and at least 4 carbon atoms, which are fluid at room temperature, The use of benzoic acid diesters of branched aliphatic diols and/or branched aliphatic diols is disclosed.

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Claims (5)

【特許請求の範囲】[Claims] 1.環境的適合性の高い脂肪および/または油、とりわけエステルを基材とする 油圧油において使用する際に、少なくとも部分的に芳香族基本構造を持つ活性物 質、例えば抗酸化剤および/または腐食防止剤の為の、低揮発性環境温和性溶剤 としての、選択した、常温で流動性がある、少なくとも4の炭素原子を持つ直鎖 および/または分枝状脂肪族ジオールの安息香酸ジエステルの使用。1. Based on environmentally compatible fats and/or oils, especially esters Active substances with an at least partially aromatic basic structure when used in hydraulic fluids low volatility environmentally friendly solvents for substances such as antioxidants and/or corrosion inhibitors a selected linear chain having at least 4 carbon atoms, fluid at room temperature, as and/or the use of benzoic acid diesters of branched aliphatic diols. 2.使用する安息香酸/ジオールのジエステルが、0℃以下の、好ましくは−1 0℃以下の流動点、および150度より低くない、好ましくは200℃以上の引 火点を持ち、エステル化したジオールの両水酸基間に直鎖状の好ましくは4〜9 の炭素原子、より好ましくは5〜7の炭素原子を含み、場合により好ましくは3 までの炭素原子を含む低級アルキル基によって1回以上置換されていることを特 徴とする請求項1に記載の使用。2. The temperature of the benzoic acid/diol diester used is below 0°C, preferably -1 Pour point below 0°C and draw point not below 150°C, preferably above 200°C. A linear chain between both hydroxyl groups of the esterified diol, preferably 4 to 9, has a flash point. of carbon atoms, more preferably 5 to 7 carbon atoms, optionally preferably 3 substituted one or more times by a lower alkyl group containing up to 2. The use according to claim 1 as a sign. 3.安息香酸ジエステルを、活性物質含量が好ましくは約5〜40重量%である 特に濃厚な活性物質溶液の製造の為に使用することを特徴とする請求項1または 2に記載の使用。3. The benzoic acid diester has an active substance content of preferably about 5-40% by weight. 1 or 2, characterized in that it is used for the production of particularly concentrated active substance solutions; Use as described in 2. 4.多くとも10の炭素原子を含むジオールの安息香酸ジエステルを溶剤として 使用することを特徴とする請求項1〜3のいずれかに記載の使用。4. Benzoic acid diesters of diols containing at most 10 carbon atoms as solvents Use according to any one of claims 1 to 3, characterized in that it is used. 5.安息香酸ジエステルをポリ−α−オレフィンとの、混合比95:5〜5:9 5である混合物にして使用することを特徴とする請求項1〜4のいずれかに記載 の使用。5. Mixing ratio of benzoic acid diester to poly-α-olefin: 95:5 to 5:9 5. According to any one of claims 1 to 4, the mixture is used as a mixture of Use of.
JP91502392A 1989-12-09 1990-12-03 Low volatility solvent for active substances containing aromatic components Pending JPH05502262A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE3940803A DE3940803A1 (en) 1989-12-09 1989-12-09 EFFECTIVE SOLVENTS FOR FLAVORING ACTIVE INGREDIENTS
DE3940803.5 1989-12-09
PCT/EP1990/002083 WO1991009096A2 (en) 1989-12-09 1990-12-03 Non-volatile solvent for aroma-containing active ingredients

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Publication Number Publication Date
JPH05502262A true JPH05502262A (en) 1993-04-22

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EP (1) EP0505484A1 (en)
JP (1) JPH05502262A (en)
CA (1) CA2098109A1 (en)
DE (1) DE3940803A1 (en)
WO (1) WO1991009096A2 (en)

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DE10137130C1 (en) * 2001-07-30 2003-03-13 Excor Korrosionsforschung Gmbh Vapor phase corrosion inhibitors, process for their preparation and use
US8299004B2 (en) 2007-04-23 2012-10-30 Idemitsu Kosan Co., Ltd. Hydraulic fluid and hydraulic system
CN114317083B (en) * 2021-12-31 2022-09-13 上海恩坤工业技术有限公司 Lubricating composition, preparation method and lubricating method

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US3505230A (en) * 1967-03-29 1970-04-07 Monsanto Co Functional ester base fluids containing corrosion inhibitors
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DE3940803A1 (en) 1991-06-13
WO1991009096A2 (en) 1991-06-27
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WO1991009096A3 (en) 1991-07-25
CA2098109A1 (en) 1991-06-10

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