DE1031921B - Brake fluids - Google Patents
Brake fluidsInfo
- Publication number
- DE1031921B DE1031921B DEW11857A DEW0011857A DE1031921B DE 1031921 B DE1031921 B DE 1031921B DE W11857 A DEW11857 A DE W11857A DE W0011857 A DEW0011857 A DE W0011857A DE 1031921 B DE1031921 B DE 1031921B
- Authority
- DE
- Germany
- Prior art keywords
- glycol
- volume
- liquid
- percent
- brake fluid
- 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
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/082—Inorganic acids or salts thereof containing nitrogen
- C10M2201/083—Inorganic acids or salts thereof containing nitrogen nitrites
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/085—Phosphorus oxides, acids or salts
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/087—Boron oxides, acids or salts
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/046—Hydroxy ethers
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix 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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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/289—Partial esters containing free hydroxy groups
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/402—Castor oils
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/26—Amines
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
Description
DEUTSCHESGERMAN
Gegenstand des Patents 850 053 ist die Zusammensetzung von Bremsflüssigkeiten aus 10 bis 25 Volumprozent Mono- und Diricinoleaten aliphatischer Glykole, 3 bis 15 Volumprozent aliphatischer Glykole, 10 bis 24 Volumprozent 2-Methyl-2,4-pentandiol sowie 45 bis 70 Volumprozent niederer einwertiger Alkohole oder niederer Monoalkyläther des Mono- bzw. Diäthylen- oder -propylenglykols. The subject of patent 850 053 is the composition of brake fluids from 10 to 25 percent by volume Mono- and diricinoleates of aliphatic glycols, 3 to 15 percent by volume of aliphatic glycols, 10 to 24 percent by volume 2-methyl-2,4-pentanediol and 45 to 70 percent by volume of lower monohydric alcohols or lower monoalkyl ethers of mono- or diethylene or -propylene glycol.
Die Erfindung kennzeichnet sich demgegenüber durch einen weiteren Gehalt von im wesentlichen wasserunlöslichen Polypropylenglykol eines mittleren Molgewichtes von 1000 bis 3000, vorzugsweise etwa 2000.In contrast, the invention is characterized by a further content of essentially water-insoluble Polypropylene glycol with an average molecular weight of 1000 to 3000, preferably about 2000.
Der Gehalt an diesem Polypropylenglykol beträgt vorzugsweise 5 bis 20 Volumteile der Gesamtflüssigkeit.The content of this polypropylene glycol is preferably 5 to 20 parts by volume of the total liquid.
An eine zufriedenstellende Bremsflüssigkeit werden folgende Ansprüche gestellt:The following requirements are made of a satisfactory brake fluid:
Die Bremsflüssigkeit muß einen so hohen Siedepunkt haben, daß sie während des Gebrauchs nicht verdampft. Sie darf selbst in sehr tiefen Wintertemperaturen nicht erstarren oder fest werden. Bei der tiefsten umgebenden Temperatur darf die Viskosität der Bremsflüssigkeit nicht über etwa 2200 cP betragen. Die Bremsflüssigkeit darf Metall nicht angreifen und die Gummiabdichtungen nicht schwellen oder zerstören. Ebenso sind gute Schmierfähigkeit, Wasserverträglichkeit, Wärmestabilität und Mischbarkeit mit anderen Bremsflüssigkeiten erforderlich.The brake fluid must have a boiling point so high that it does not evaporate during use. It must not freeze or solidify even in very low winter temperatures. At the deepest surrounding Temperature, the viscosity of the brake fluid must not exceed approx. 2200 cP. The brake fluid is allowed Do not attack metal and do not swell or destroy the rubber seals. Good lubricity, Water compatibility, thermal stability and miscibility with other brake fluids required.
Diese Forderungen und auch der Anspruch, daß der Schmiermittelbestandteil in Wasser unlöslich ist, werden erfindungsgemäß dadurch erfüllt, daß der Schmiermittelbestandteil bei der erfindungsgemäßen Bremsflüssigkeit zum Teil aus Glykolricinoleat und zum Teil aus Polypropylenglykol besteht.These requirements and also the requirement that the lubricant component is insoluble in water become according to the invention fulfilled in that the lubricant component in the brake fluid according to the invention consists partly of glycol ricinoleate and partly of polypropylene glycol.
Die erfindungsgemäße Bremsflüssigkeit enthält als wasserunlöslichen Schmiermittelbestandteil ein Gemisch aus einem Ricinoleat eines aliphatischen Glykols und einem wasserunlöslichen Polypropylenglykol mit einem mittleren Molekulargewicht von 1000 bis 3000. Als Verdünnungsbestandteil enthält diese Flüssigkeit ein Verdünnungsmittel aus der Gruppe der Propylalkohole, Butylalkohole, Amylalkohole, Methoxybutanol und den niederen Monoalkyläthern von Äthylenglykol und Diäthylenglykol. Außerdem eine verhältnismäßig kleine Menge eines Glykols oder mehrerer Glykole, wie Propylenglykol, Butylenglykol oder Hexylenglykol, und ein Korrosionsschutzmittel sowie ein Oxydationsschutzmittel.The brake fluid according to the invention contains a mixture as a water-insoluble lubricant component from a ricinoleate of an aliphatic glycol and a water-insoluble polypropylene glycol with a average molecular weight from 1000 to 3000. This liquid contains a diluent as a diluent from the group of propyl alcohols, butyl alcohols, amyl alcohols, methoxybutanol and the lower monoalkyl ethers of ethylene glycol and diethylene glycol. In addition, a relatively small one Amount of one or more glycols, such as propylene glycol, butylene glycol or hexylene glycol, and a Anti-corrosion agent and an anti-oxidation agent.
Die Masse besteht aus 10 bis 25 Volumprozent eines Ricinoleates eines Glykols, das ein aliphatisches Glykol mit nicht mehr als fünf Kohlenstoffatomen je Molekül ist, aus 3 bis 15 Volumprozent eines wasserunlöslichen Polypropylenglykols mit einem durchschnittlichen Molekulargewicht von 1000 bis 3000, ferner von 45 bis 70 Volumprozent von wenigstens einem Verdünnungsmittel aus der Gruppe der Propylalkohole, Butylalkohole, Amylalkohole, Methoxybutanol und der niederen Mono-Brems flüssigkeitenThe mass consists of 10 to 25 percent by volume of a ricinoleate of a glycol, which is an aliphatic glycol with no more than five carbon atoms per molecule, from 3 to 15 percent by volume of a water-insoluble one Polypropylene glycol with an average molecular weight of 1000 to 3000, also from 45 to 70 percent by volume of at least one diluent from the group of propyl alcohols, butyl alcohols, Amyl alcohols, methoxybutanol and the lower mono brake fluids
Zusatz zum Patent 850 053Addition to patent 850 053
Anmelder:Applicant:
Wagner Electric Corporation,
St. Louis, Mo. (V. St. A.)Wagner Electric Corporation,
St. Louis, Mo. (V. St. A.)
Vertreter: Dr.-Ing. H. Ruschke,Representative: Dr.-Ing. H. Ruschke,
Berlin-Friedenau, Lauterstr. 37,Berlin-Friedenau, Lauterstr. 37,
und Dipl.-Ing. K. Grentzenberg, München 27,and Dipl.-Ing. K. Grentzenberg, Munich 27,
PatentanwältePatent attorneys
Beanspruchte Priorität:
V. St. v. Amerika vom 9. August 1962Claimed priority:
V. St. v. America 9 August 1962
George L. Doelling und Chester B. Swander,George L. Doelling and Chester B. Swander,
St. Louis, Mo, (V. St. A.),
sind als Erfinder genannt wordenSt. Louis, Mo., (V. St. A.),
have been named as inventors
alkyläther von Äthylen- und Diäthylenglykol, ferner aus 10 bis 24 Volumprozent wenigstens eines Glykols der
Gruppe aus Propylenglykol, Butylenglykol und Hexylenglykol, gewünschtenfalls zusammen mit einem Korrosionsschutzmittel
und einem Oxydationsschutzmittel.
In dem Schmiermittelbestandteil der Flüssigkeit werden die Ricinoleate der niederen aliphatischen Glykole
und Diglykole bevorzugt, da diese sehr stabil sind, der Flüssigkeit gute Schmiereigenschaften geben und die
Flüssigkeit nicht zum Ausfrieren bei niederen Temperaturen bringen, wie dies bei Rizinusöl der Fall ist.alkyl ethers of ethylene and diethylene glycol, furthermore from 10 to 24 percent by volume of at least one glycol from the group consisting of propylene glycol, butylene glycol and hexylene glycol, if desired together with an anti-corrosion agent and an anti-oxidation agent.
In the lubricant component of the liquid, the ricinoleates of the lower aliphatic glycols and diglycols are preferred because these are very stable, give the liquid good lubricating properties and do not cause the liquid to freeze out at low temperatures, as is the case with castor oil.
Propylenglykolmonoricinoleat ist der bevorzugte Ricinoleatester dieser Masse. Diäthylenglykolricinoleat und Butylenglykolricinoleat können ebenfalls verwendet werden. Ein im wesentlichen wasserunlöslicher Polypropylenglykol mit einem durchschnittlichen Molekulargewicht von 1000 bis 3000 kann ebenfalls in dem Schmiermittelbestandteil der Flüssigkeit verwendet werden. Das bevorzugte Polypropylenglykol hat ein mittleres Molekulargewicht von etwa 2000. Dieses Erzeugnis hat eine Viskosität, die etwas niedriger ist als die des Rizinusöls, und etwa 200E bei 37,80C gegen etwa 400E für Rizinusöl beträgt. Genau wie Rizinusöl ist auch die Schwellwirkung auf Gummi sehr gering.Propylene glycol monoricinoleate is the preferred ricinoleate ester of this composition. Diethylene glycol ricinoleate and butylene glycol ricinoleate can also be used. A substantially water-insoluble polypropylene glycol having an average molecular weight of 1,000 to 3,000 can also be used in the lubricant component of the liquid. The preferred polypropylene glycol having an average molecular weight of about 2000. This product has as the E and about 20 0 37.8 0 C to about 40 0 E is a viscosity which is somewhat lower than the castor oil, for castor oil. Just like castor oil, the swelling effect on rubber is very low.
Das Verdünnungsmittel oder das die Viskosität vermindernde Mittel der bevorzugten Flüssigkeit kann einThe diluent or viscosity reducing agent of the preferred liquid can be
80S 530/38580S 530/385
Alkohol, ζ. B. Normal-Butanol oder Isobutanol, ein .Alcohol, ζ. B. normal butanol or isobutanol.
Glykoläther, z. B. 3-Methoxybutanol oder Diäthylen- Beispiel δ Glycol ethers, e.g. B. 3-methoxybutanol or diethylene example δ
glykolmonoäthyläther oder ein anderer niederer Alkyl- Diäthylenglykolmonoäthyläther ... 70,0 Volumprozent äther von Äthylenglykol oder Diäthylenglykol sein. Bei Polypropylenglykolglycol monoethyl ether or another lower alkyl diethylene glycol monoethyl ether ... 70.0 percent by volume ether of ethylene glycol or diethylene glycol. For polypropylene glycol
Verwendung von Diäthylenglykolmonoäthyläther als 5 (Molekulargewicht 2000) 11,5 „Use of diethylene glycol monoethyl ether as 5 (molecular weight 2000) 11.5 "
Verdünnungsmittel sollte die reine Qualität von geringem Propylenglykol 5,0 „Diluent should be the pure quality of low propylene glycol 5.0 "
spezifischem Gewicht verwendet werden, da das handeis- Propylenglykolmonoricinoleat 12,5 „specific weight, as the commercial propylene glycol monoricinoleate 12.5 "
übliche Erzeugnis bis zu 20% oder mehr Äthylenglykol Diphenylpropan 0,3 „common product up to 20% or more ethylene glycol diphenylpropane 0.3 "
enthalten kann, also für Verwendung in dieser Mischung Kaliumricinoleat 0,7 „may contain, so for use in this mixture potassium ricinoleate 0.7 "
nicht geeignet ist. iois not suitable. ok
Zur Verhütung einer Korrosion der Metallteile der Die durch Mischeil dieser Bestandteile erhalteneTo prevent corrosion of the metal parts of the die obtained by mixing these components
Bremsanlage wird em Konrosionsschutzmittel verwendet. Bremsflüssigkeit hat folgende Eigenschaften: Kaliumricinoleat, Borax, Natriumnitrit oder Diamyl-Brake system is used as an anti-corrosion agent. Brake fluid has the following properties: Potassium ricinoleate, borax, sodium nitrite or diamyl
aminphosphat können verwendet werden. Ebenso kann Spezifisches Gewicht bei 2O0C 0,993amine phosphate can be used. The specific weight at 2O 0 C can also be 0.993
ein Oxydationsschutzmittel wie Diphenylolpropan oder 15 Säurezahl 0,17an antioxidant such as diphenylolpropane or 15 acid number 0.17
Hydrochinon oder 2,6-Di-tertiär-butyl-4-methylphenol Viskosität bei — 400C 89,5 0EHydroquinone or 2,6-di-tertiary-butyl-4-methylphenol viscosity at - 40 0 C 89.5 0 E
zugesetzt werden. Für die Zwecke genügt ein Zusatz Viskosität bei 18,90C 2,120Ecan be added. For the purpose of an additional sufficient viscosity at 18.9 0 C 2.12 0 E
von 0,2 bis 3,0% des Korrosionsschutzmittels und 0,1 Siedepunkt, SAE 1940Cfrom 0.2 to 3.0% of the corrosion protection agent and 0.1 boiling point, SAE 194 0 C
bis 0,3% des Oxydationsschutzmittels, berechnet auf Kaltversuch (6 Stunden bei -510C) flüssigto 0.3% of Oxydationsschutzmittels, calculated on cold test (6 hours at -51 0 C) liquid
das Gewicht der Flüssigkeit. 20the weight of the liquid. 20th
Die Mengenverhältnisse der in der Mischung verwen- Der SAE-Korrosionsversuch, 5 Tage bei 100° C, ergabThe proportions of the used in the mixture. The SAE corrosion test, 5 days at 100 ° C, resulted
deten Bestandteile sind ausschlaggebend, und die bean- mit dieser Flüssigkeit sehr zufriedenstellende Ergebnisse, spruchten Mengenverhältnisse sind ausgewählt, weil die Der Gewichtsverlust von Zinn, Stahl, Aluminium, Gußzahlreichen Forderungen an eine industriell benutzbare eisen, Messing und Kupfer betrug weniger als 0,1 mg/cm2, Bremsflüssigkeit nur dann erfüllt werden, wenn diese 25 d. h. sehr viel weniger, als die SAE-Normen zulassen. Mengenverhältnisse verwendet sind. Die Gummischwellung nach 5 Tagen bei 70° C anThe particular components are decisive, and the results obtained with this liquid are very satisfactory. The proportions required are selected because the weight loss of tin, steel, aluminum, cast iron, brass and copper required many industrial uses was less than 0.1 mg / cm 2 , brake fluid can only be met if it is 25, ie much less than the SAE standards allow. Quantities are used. The rubber swelling started after 5 days at 70 ° C
Die nachstehenden Beispiele dienen zur Erläuterung einem 31-mm-Manhatten-Becher betrug 4,95 Volumder Erfindung. Die Beispiele, die die verschiedenen Ver- prozent.The following examples are illustrative of a 31 mm Manhattan cup was 4.95 volumes Invention. The examples showing the different percentages.
hältnisse und Mengen erläutern, ergeben etwa 100 ecm Beispiel 3Explaining proportions and quantities result in about 100 ecm Example 3
Flüssigkeit. 3°Liquid. 3 °
Diäthylenglykolmonoäthyläther .. 60,00 Volumprozent Beispiel 1 PolypropylenglykolDiethylene glycol monoethyl ether .. 60.00 percent by volume Example 1 Polypropylene glycol
Diäthylenglykolmonoäthyläther ... 65 Volumprozent (Molekulargewicht 2000) 7,5Diethylene glycol monoethyl ether ... 65 percent by volume (molecular weight 2000) 7.5
Polypropylenglykol Propylenglykol 4,2Polypropylene glycol propylene glycol 4.2
(Molekulargewicht 2000) 11,5 „ 35 2-Methyl-2,4-pentandiol 10,0(Molecular weight 2000) 11.5 "35 2-methyl-2,4-pentanediol 10.0
2-Methyl-2,4-pentandiol Propylenglykolmonoricinoleat 17,0 „2-methyl-2,4-pentanediol propylene glycol monoricinoleate 17.0 "
(Hexylenglykol) 5,0 „ Diphenylpropan 0,3(Hexylene glycol) 5.0 "diphenylpropane 0.3
Propylenglykol 5,0Propylene glycol 5.0
Propylenglykolrnonoricinoleat 12,5Propylene glycol nonoricin oleate 12.5
Diphenylpropan 0,3Diphenylpropane 0.3
Kaliumricinoleat 0,7Potassium ricinoleate 0.7
Kaliumricinoleat 1,0 „Potassium ricinoleate 1.0 "
40 Die durch Mischen dieser Bestandteile erhaltene Bremsflüssigkeit hatte folgende Eigenschaften:40 The brake fluid obtained by mixing these components had the following properties:
Spezifisches Gewicht bei 200C 0,984Specific gravity at 20 0 C 0.984
Die aus diesen Bestandteilen gemischte Bremsflüssig- Säurezahl 0,16The brake fluid acid number mixed from these components is 0.16
keit hatte folgende Eigenschaften: Viskosität bei 200C 2,30Eness had the following properties: viscosity at 20 0 C 2.3 0 E
, . Gummischwellwert, 5 Tage bei 700C,,. Rubber threshold, 5 days at 70 0 C,
Spezifisches Gewicht bei 20 C 0,9905 Zunahme in Volumprozent 4,7%Specific weight at 20 C 0.9905 Increase in percentage by volume 4.7%
Farbe, Parlin-Skala 3 Siedepunkt ; 192°CColor, Parlin scale 3 boiling point; 192 ° C
PH-Wert, elektrometnsch 8,82 Kaltversuch (6 Stunden bei - 51° C) flüssigPH value, electromechanical 8.82 cold test (6 hours at - 51 ° C) liquid
Säurezahl 0,14 v ' 5 Acid number 0.14 v ' 5
Viskosität bei 37,80C 1,7°E 50 _ ..... ,CA~T, . ,e~ , . innon Viscosity at 37.8 0 C 1.7 ° E 50 _ ....., CA ~ T. , e ~,. innon
y ν 'ft b ' -4O0C 1060E Der ubhche SAE-Korrosionsversuch, 5 Tage bei 100 C,y ν 'ft b' -4O 0 C 106 0 E The ubhche SAE corrosion test, 5 days at 100 C,
Flammpunkt '.'.'.'.'.'.'.'.'.'.'.'.'.'.'.'.'.'.'.'.'. 101,7° C ergab fol^ende Verluste in mS/cm2: Flash point '.'. '.'. '.'. '.'. '.'. '.'. '.'. '.'. '.'. '.'. '.'. 101.7 ° C er g from the following losses in m S / cm2:
Siedepunkt : 196,1° C Verzinntes Eisen 0,04Boiling point: 196.1 ° C. Tinned iron 0.04
Gummischwellwert , bei70°C Stahl 0,17Rubber threshold, at 70 ° C steel 0.17
Gewichtszunahme nach 16 Stunden 4,23 % 55 Aluminium — 0,02Weight gain after 16 hours 4.23% 55 aluminum - 0.02
Erstarrungspunkt (6 Stunden bei —510C) ... flüssig Gußeisen 0,13Freezing point (6 hours at -51 0 C) ... liquid cast iron 0.13
Messing 0,12Brass 0.12
Der Korrosionsversuch nach den SAE-Vorschriften Kupfer 0,02The corrosion test according to the SAE regulations copper 0.02
für hydraulische Bremsflüssigkeiten (Standard of Auto- Alle diese Werte lagen weit unter den Grenzwertenfor hydraulic brake fluids (Standard of Auto- All these values were well below the limit values
motive Engineers, Normen der Automobil-Ingenieure) 60 der Vorschrift.motive engineers, standards of automotive engineers) 60 of the regulation.
wurde bei 100°C während 5 Tagen mit dieser Flüssigkeit Beispiel 4was at 100 ° C for 5 days with this liquid Example 4
durchgeführt. Der Aluminiumstreifen zeigte keinencarried out. The aluminum strip showed none
Gewichtsverlust. Verzinntes Eisen, Stahl, Gußeisen und 3-Methoxybutanol-3 55,0 VolumprozentWeight loss. Tin-plated iron, steel, cast iron and 3-methoxybutanol-3 55.0 percent by volume
Kupfer verloren je etwa 0,02 mg/cm2. Der Messing- PolypropylenglykolCopper lost about 0.02 mg / cm 2 each. The brass polypropylene glycol
Streifenverlust betrug 0,06 mg/cm2. Alle diese Ergebnisse 65 (Molekulargewicht 2000) 10,0 „Stripe loss was 0.06 mg / cm 2 . All of these results 65 (molecular weight 2000) 10.0 "
lagen weit unter dem durch die Vorschriften züge- Propylenglykol 6,7 „were far below the train regulations propylene glycol 6.7 "
lassenen Verlust, der für Messing und Kupfer 0,5, für 2-Methyl-2,4-pentandiol 10,0 „allowable loss, 0.5 for brass and copper, 10.0 for 2-methyl-2,4-pentanediol
Zinn, Stahl und Gußeisen 0,7 und für Aluminium Propylenglykolmonoricinoleat 17,0 „Tin, steel and cast iron 0.7 and for aluminum propylene glycol monoricinoleate 17.0 "
0,2 mg/cm2 beträgt. Nach der Korrosion war der pH-Wert Diphenylolpropan 0,3 „0.2 mg / cm 2 . After the corrosion of the pH value was 0.3 diphenylolpropane "
gleich 7,6. 70 Kaliumricinoleat 1,0 „equal to 7.6. 70 potassium ricinoleate 1.0 "
Die durch Mischen dieser Bestandteile erhaltene Bremsflüssigkeit hat folgende Eigenschaften:The brake fluid obtained by mixing these components has the following properties:
Spezifisches Gewicht bei 20° C 0,951Specific gravity at 20 ° C 0.951
Siedepunkt 1600CBoiling point 160 ° C
Viskosität bei 200C 2,75°EViscosity at 20 0 C ° 2.75 E
Kaltversuch (6 Stunden bei —510C) flüssigCold test (6 hours at -51 0 C) liquid
Gummischwellung, 5 Tage bei 700C,Rubber swelling, 5 days at 70 0 C,
Zunahme in Volumprozent 4,5 %Increase in volume percentage 4.5%
Eine sogenannte »arktische« Flüssigkeit wurde durch Mischen folgender Bestandteile in folgenden Mengen erhalten:A so-called "arctic" liquid was made by mixing the following ingredients in the following amounts obtain:
Normal-Butanol 50,0 VolumprozentNormal butanol 50.0 percent by volume
Diäthylenglykolmonoäthyläther ... 24,7 „Diethylene glycol monoethyl ether ... 24.7 "
PolypropylenglykolPolypropylene glycol
(Molekulargewicht 2000) 7,3(Molecular weight 2000) 7.3
Propylenglykol 6,1 „Propylene glycol 6.1 "
2-Methyl-2,4-pentandiol 3,02-methyl-2,4-pentanediol 3.0
Propylenglykolmonoricinoleat 8,0 „Propylene glycol monoricinoleate 8.0 "
2,6-Di-tertiär-butyl-4-methylphenol 0,1 „2,6-di-tert-butyl-4-methylphenol 0.1 "
Kaliumricinoleat 0,5 ,,Potassium ricinoleate 0.5 ,,
Die aus diesen Bestandteilen gemischte »arktische« Bremsflüssigkeit hatte einen Siedepunkt von 1300C. Die Gummischwellung, 5 Tage bei 70° C, auf einem 31-mm-Manhatten-Normalbecher ergab eine Zunahme im Fußdurchmesser von 0,94 mm. In einem Kaltversuch (6 Tage bei —53° C) war die Flüssigkeit im wesentlichen klar und ziemlich flüssig. Der Flammpunkt (Cleveland) war 600C. Das spezifische Gewicht bei 200C betrug 0,9031, und der pH-Wert, gemessen nach der SAE-Vorschrift, war 9,1. Nach Zusatz von 5% Wasser und weiterem Stehenlassen während 24 Stunden bei —53° C war die Mischung immer noch flüssig. Diese Bremsflüssigkeit arbeitet selbst bei sehr tiefen Temperaturen. Nach 6 Stunden war sie bei —67,8° C immer noch flüssig.The mixed from these components "Arctic" brake fluid had a boiling point of 130 mm 0 C. The rubber swelling, 5 days at 70 ° C, on a 31-mm-Manhatten normal cups showed an increase in base diameter of 0.94. In a cold test (6 days at -53 ° C) the liquid was essentially clear and fairly runny. The flash point (Cleveland) was 60 0 C. The specific gravity at 20 0 C was 0.9031, and the pH value, measured according to the SAE requirement, was 9.1. After adding 5% water and allowing it to stand for 24 hours at -53 ° C, the mixture was still liquid. This brake fluid works even at very low temperatures. After 6 hours it was still liquid at -67.8 ° C.
Normal-Butanol 50,0 VolumprozentNormal butanol 50.0 percent by volume
PolypropylenglykolPolypropylene glycol
(Molekulargewicht 1200) 19,0(1200 molecular weight) 19.0
Propylenglykol 9,0 „Propylene glycol 9.0 "
l-Methyl-2,4-pentandiol 15,01-methyl-2,4-pentanediol 15.0
Diäthylenglykolmonoricinoleat .... 6,0 ,,Diethylene glycol monoricinoleate .... 6.0 ,,
Hydrochinon 0,125 „Hydroquinone 0.125 "
Diamylamin 0,75 „Diamylamine 0.75 "
Phosphorsäure (85 %) 0,125Phosphoric acid (85%) 0.125
Die durch Mischen dieser Bestandteile erhaltene Bremsflüssigkeit hatte folgende Eigenschaften:The brake fluid obtained by mixing these components had the following properties:
Spezifisches Gewicht bei 20° C .... 0,899Specific weight at 20 ° C .... 0.899
Siedepunkt 129°CBoiling point 129 ° C
Flammpunkt (Cleveland) 57° CFlash point (Cleveland) 57 ° C
Gummischwellung, 16 Stunden bei 7O0C, Manhatten-31-mm-Becher,Gum swelling, 16 hours at 7O 0 C, Manhattan-31 mm cup,
Zunahme in Gewichtsprozent ... 2,82 °/0 Increase in percent by weight ... 2.82% / 0
pH-Wert, SAE-Verfahren 8,3p H value, SAE method 8.3
Kalt versuch (3 Tage bei —400C).. flüssig, jedoch warCold trial (3 days at -40 0 C) .. liquid, but was
die Viskosität ziemlieh hochthe viscosity is fairly high
Isobutanol 60,0 VolumprozentIsobutanol 60.0 percent by volume
PolypropylenglykolPolypropylene glycol
(Molekulargewicht 2725) 11,5(Molecular weight 2725) 11.5
2-Methyl-2,4-pentandiol 10,02-methyl-2,4-pentanediol 10.0
Propylenglykolmonoricinoleat . ... 12,5 ,,Propylene glycol monoricinoleate. ... 12.5 ,,
Diphenylpropan 0,3 „Diphenylpropane 0.3 "
Kaliumricinoleat 0,7 „Potassium ricinoleate 0.7 "
Die durch Mischen dieser Bestandteile erhaltene Bremsflüssigkeit hatte folgende Eigenschaften:The brake fluid obtained by mixing these components had the following properties:
Spezifisches Gewicht bei 20° C 0,876Specific weight at 20 ° C 0.876
Farbe, Parlin-Skala 2Color, Parlin Scale 2
Flammpunkt (Cleveland) 460CFlash point (Cleveland) 46 0 C
Siedepunkt 114°CBoiling point 114 ° C
Säurezahl 0,09Acid number 0.09
pH-Wert, SAE-Verfahren 8,98p H value, SAE method 8.98
Viskosität, SSU bei 200C 100Viscosity, SSU at 20 0 C 100
Kaltversuch (3 Tage bei — 400C) ziemlichCold test (3 days at - 40 0 C) pretty
flüssigfluid
Gummischwellung (5 Tage bei 700C), Zunahme im Durchmesser eines 31-mm-Bechers 0,94mmRubber swelling (5 days at 70 0 C), increase in diameter of a 31 mm cup 0,94mm
Äthylenglykolmono-N-butyläther .. 45 VolumprozentEthylene glycol mono-N-butyl ether .. 45 percent by volume
Normal-Propanol 15 „Normal propanol 15 "
1,3-Butylenglykol 6,31,3-butylene glycol 6.3
PolypropylenglykolPolypropylene glycol
(Molekulargewicht 1025) 17,5(Molecular weight 1025) 17.5
!,S-Butylenglykolmonoricinoleat ... 15,0 „!, S-butylene glycol monoricinoleate ... 15.0 "
Kaliumricinoleat 1,1 ,,Potassium ricinoleate 1.1 ,,
2,6-Di-tertiär-butyl-4-methylphenol 0,1 „2,6-di-tert-butyl-4-methylphenol 0.1 "
Die durch Mischen dieser Bestandteile erhaltene Bremsflüssigkeit hatte folgende Eigenschaften:The brake fluid obtained by mixing these components had the following properties:
Spezifisches Gewicht bei 2O0C 0,9287Specific gravity at 2O 0 C 0.9287
Flammpunkt (Cleveland) 57°CFlash point (Cleveland) 57 ° C
Siedepunkt, SAE-Verfahren 123° CBoiling point, SAE process 123 ° C
Pn-Wert, SAE-Verfahren 7,92Pn value, SAE method 7.92
Kaltversuch (16 Stunden bei —45,6° C) ziemlichCold test (16 hours at -45.6 ° C) quite
flüssigfluid
Claims (2)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US744385XA | 1952-08-09 | 1952-08-09 | |
US429390A US2803605A (en) | 1954-05-12 | 1954-05-12 | Brake fluid |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1031921B true DE1031921B (en) | 1958-06-12 |
Family
ID=26755667
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEW11857A Pending DE1031921B (en) | 1952-08-09 | 1953-08-06 | Brake fluids |
DEW16644A Pending DE1038222B (en) | 1952-08-09 | 1955-05-07 | Brake fluids |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEW16644A Pending DE1038222B (en) | 1952-08-09 | 1955-05-07 | Brake fluids |
Country Status (3)
Country | Link |
---|---|
DE (2) | DE1031921B (en) |
FR (2) | FR1088271A (en) |
GB (2) | GB744385A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1135121B (en) * | 1958-08-27 | 1962-08-23 | Iashellia Res Ltd | Hydraulic fluid |
DE1217530B (en) * | 1958-11-06 | 1966-05-26 | Inst Francais Du Petrol | Hydraulic fluid |
DE1218096B (en) * | 1961-07-26 | 1966-06-02 | Huels Chemische Werke Ag | Hydraulic fluid |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2918052A (en) * | 1957-03-14 | 1959-12-22 | Armour Res Found | Heat-releasing anti-icing means |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR976467A (en) * | 1948-01-19 | 1951-03-19 | Wagner Electric Corp | Fluid that can be used in hydraulic braking systems and devices |
-
1953
- 1953-07-29 GB GB21019/53A patent/GB744385A/en not_active Expired
- 1953-08-06 DE DEW11857A patent/DE1031921B/en active Pending
- 1953-08-07 FR FR1088271D patent/FR1088271A/en not_active Expired
-
1955
- 1955-04-29 GB GB12454/55A patent/GB783311A/en not_active Expired
- 1955-05-07 DE DEW16644A patent/DE1038222B/en active Pending
- 1955-05-12 FR FR67848D patent/FR67848E/en not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR976467A (en) * | 1948-01-19 | 1951-03-19 | Wagner Electric Corp | Fluid that can be used in hydraulic braking systems and devices |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1135121B (en) * | 1958-08-27 | 1962-08-23 | Iashellia Res Ltd | Hydraulic fluid |
DE1217530B (en) * | 1958-11-06 | 1966-05-26 | Inst Francais Du Petrol | Hydraulic fluid |
DE1230159B (en) * | 1958-11-06 | 1966-12-08 | Inst Francais Du Petrol | Hydraulic fluids |
DE1218096B (en) * | 1961-07-26 | 1966-06-02 | Huels Chemische Werke Ag | Hydraulic fluid |
Also Published As
Publication number | Publication date |
---|---|
DE1038222B (en) | 1958-09-04 |
FR67848E (en) | 1958-03-24 |
FR1088271A (en) | 1955-03-04 |
GB783311A (en) | 1957-09-18 |
GB744385A (en) | 1956-02-08 |
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