WO2004081155A1 - Dot 4 brake fluids - Google Patents

Dot 4 brake fluids Download PDF

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Publication number
WO2004081155A1
WO2004081155A1 PCT/EP2004/002552 EP2004002552W WO2004081155A1 WO 2004081155 A1 WO2004081155 A1 WO 2004081155A1 EP 2004002552 W EP2004002552 W EP 2004002552W WO 2004081155 A1 WO2004081155 A1 WO 2004081155A1
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WO
WIPO (PCT)
Prior art keywords
glycol
liquid according
weight
dot
poly
Prior art date
Application number
PCT/EP2004/002552
Other languages
German (de)
French (fr)
Inventor
Bernd Wenderoth
Bayram Aydin
Michael Roida
Ralf Strauss
Ladislaus Meszaros
Herbert Matzkait
Original Assignee
Basf Aktiengesellschaft
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Basf Aktiengesellschaft filed Critical Basf Aktiengesellschaft
Priority to BRPI0408234-6A priority Critical patent/BRPI0408234A/en
Priority to EP04719421A priority patent/EP1603996A1/en
Priority to MXPA05009288A priority patent/MXPA05009288A/en
Priority to AU2004219905A priority patent/AU2004219905A1/en
Priority to CA002517683A priority patent/CA2517683A1/en
Priority to US10/548,173 priority patent/US20060264337A1/en
Priority to JP2006500058A priority patent/JP2006519887A/en
Publication of WO2004081155A1 publication Critical patent/WO2004081155A1/en
Priority to NO20054265A priority patent/NO20054265L/en

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    • CCHEMISTRY; METALLURGY
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • 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
    • 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
    • C10M111/04Lubrication 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 macromolecular organic compound
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/0215Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms used as base material
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
    • C10M2207/0225Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups used as base material
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/024Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
    • C10M2209/1045Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only used as base material
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/105Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
    • C10M2209/1055Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only used as base material
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/108Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
    • C10M2209/1085Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified used as base material
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/20Containing nitrogen-to-oxygen bonds
    • C10M2215/202Containing nitrogen-to-oxygen bonds containing nitro groups
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids

Definitions

  • the present invention relates to new DOT 4 brake fluids in which the addition of borates (boric acid esters) is not necessary.
  • Hydraulic fluids and in particular brake fluids for motor vehicles are subject to very high requirements with regard to their chemical and physical properties.
  • DOT US Department of Transportation
  • FMVSS-No. 116 Federal Motor Vehicle Saftey Standard
  • SAE J 1704 standard published by the Society of Automotive Engineers
  • modern brake fluids are said to have high dry boiling points (reflux boiling points, dry [Equilibrium reflux boiling point, "ERBP”]) and high wet boiling points (reflux boiling points, moist ["wet ERBP”]) have, on the other hand, but also have a viscosity that changes only slightly within a wide temperature range.
  • wet boiling point "wet ERBP" > 155 ° C viscosity at -40 ° C: ⁇ 1800 mm 2 / s
  • DOT 4 brake fluids always contain boric acid esters such as methyl triglycol borate, which can chemically eliminate penetrating water from the brake fluid in certain quantities by hydrolysis.
  • boric acid esters themselves are hygroscopic, which means that such DOT 4 brake fluids are particularly useful in regions with high air humidity, for example in tropical and subtropical regions. areas can absorb so much moisture very quickly that the functionality of a brake system filled with it can be adversely affected despite the boric acid ester's collection function.
  • DOT 4 brake fluids which contain 54.5 to 92% of at least one boric acid ester, up to 20% polyalkylene glycols and 3 to 43% polyglycol monoalkyl or dialkyl ether in addition to other additives.
  • No. 3,972,822 describes DOT 4 brake fluids which contain 40 to 65% polyglycol monoalkyl ether, 16 to 45% polyglycols and 10 to 19% boric acid ester plus corrosion inhibitors.
  • WO 00/46325 describes DOT 4 brake fluids which contain methyl triglycol borate, glycol ethers and glycols in different amounts and an additive system.
  • Corresponding DOT 4 brake fluids are also disclosed in WO 02/38711, which contain different methylpolyglycol borates, polyglycol monoalkyl ethers and corrosion inhibitors.
  • DE 36 27 432 C2 describes borate-free brake fluids of 30 to 80% of a glycol component and up to 70% polyglycol alkyl ethers.
  • the glycol component in turn contains 0 to 80% by weight, preferably 55 to 80% by weight, of diethylene glycol and / or dipropylene glycol.
  • the polyglycol alkyl ether component contains 0 to 90% by weight, preferably 0 to 50% by weight, of at least one polyglycol monoalkyl ether.
  • the object of the present invention is to provide such a brake fluid.
  • This brake fluid should preferably be less hygroscopic and usable in regions with high air humidity.
  • the conversion should only require small amounts of boric acid esters or, ideally, even be completely unnecessary. This object is achieved by containing a brake fluid
  • liquids according to the invention are free from boric acid esters.
  • Diethylene glycol or dipropylene glycol or a mixture of diethylene glycol and dipropylene glycol can be used in any ratio.
  • Diethylene glycol is preferred.
  • Diethylene glycol and / or dipropylene glycol are present in the brake fluids according to the invention in an amount of 10 to 50% by weight, preferably 20 to 40% by weight.
  • Another component of the brake fluids according to the invention are one or more monoalkyl ethers of (poly) ethylene glycols and / or (poly) propylene glycols, which are present in the fluids according to the invention in an amount of 50 to 90% by weight, preferably 60 to 80% by weight, available. ,
  • Suitable (poly) ethylene glycols are monoethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, pentaethylene glycol and hexaethylene glycol.
  • Suitable (poly) propylene glycols are monopropylene glycol, dipropylene glycol, tripropylene glycol, tetrapropylene glycol, pentapropylene glycol and hexapropylene glycol.
  • Diethylene glycol, triethylene glycol and / or tetraethylene glycol are preferred.
  • the alkyl radical in the monoalkyl ethers of (poly) ethylene glycol and (poly) propylene glycol used according to the invention is preferably a linear or branched - - alkyl radical. It is more preferred to use a linear or branched C4-alkyl radical, for example methyl, ethyl, i-propyl, n-propyl, n-butyl, i-butyl, sec-butyl or tert-butyl.
  • alkyl radicals are methyl, ethyl, i-propyl or n-butyl.
  • the use of methyldiethylene glycol, methyltriethylene glycol, methyltetraethylene glycol and or butyltriethylene glycol is preferred.
  • the brake fluids according to the invention have wet boiling points and, in particular, dry boiling points which are those which have hitherto been achieved with borate-free brake fluids. They are comparable to those that have so far only been achieved with liquids containing borate. Due to the absence of borate, the liquids according to the invention are significantly less hygroscopic than those containing borate. This is particularly advantageous when used in tropical and subtropical areas, since part of the water is bound by the addition of borate, but water is also absorbed relatively quickly. This results in a deterioration in the quality of the brake fluid. In particular, this loss of quality often occurs in the braking system of motor vehicles, but also during the storage and transportation of the liquids.
  • the brake fluids according to the invention do not have the disadvantages mentioned.
  • the brake fluids according to the invention can contain boric acid esters in different amounts.
  • the advantages of low hygroscopicity according to the invention are generally not achieved in this way. This is especially the case when the amounts of boric acid esters customary according to the prior art are added.
  • liquids according to the invention are in particular free from polyalkylene glycol dialkyl ethers. Although these may also be present in different amounts, the advantages of the brake fluids according to the invention, in particular the compatibility with rubber and sealing materials, are generally not achieved, this of course also depending on the amount of polyalkylene glycol dialkyl ethers that may be present ,
  • polyglycols can be contained in the formulation bars according to the invention as an optional component.
  • Higher-boiling reaction products of ethylene oxide and / or propylene oxide and / or butylene oxide with water or diols are preferably used.
  • reaction products of mixtures of ethylene oxide and propylene oxide with water are used.
  • the number of alkylene oxide units in the polyglycols mentioned is generally 2 to 10, preferably 2 to 3 and in an amount of up to 5%.
  • the effect of these high-boiling polyglycols is that of a reducing agent, which is essentially due to an improvement in the temperature-viscosity behavior.
  • the polyglycols give the polyglycols, which are often thin at high temperatures, colmonoalkyl ethers have sufficient viscosity and thus ensure adequate lubrication. Adequate lubrication is desirable since rubber or elastomers on metal in the components of the motor vehicle brake system must slide as wear-free as possible.
  • the DOT 4- according to the invention contain
  • Brake fluids for motor vehicles further 0.001 to 10% by weight, preferably 0.005 to 4% by weight 5, in particular 0.005 to 1% by weight, of one or more corrosion inhibitors, for example 1H-1, 2,3-benzotriazole, 1H-1 , 2,3-tolutriazole, hydrogenated 1H-1,2,3-tolutriazole, benzimidazole and / or their derivatives, alkali metal salts of phosphoric acid and phosphorous acid, fatty acids, preferably caprylic, lauric, palmitic, stearic or oleic acid and their alkali metal salts, Esters of phosphoric acid and phosphorous acid, preferably ethyl phosphate, dimethyl phosphate, isopropyl phosphate, disopropyl phosphate, butyiphosphite or dimethyl phosphite, optionally ethoxylated mono- and dialkylamines and their salts with mineral and fatty acids,
  • R atom in each case independently of other radicals R present, a hydrogen or denotes a radical R 1, R 1 , each independently of other radicals R 1 , alkyl, aryl, aralkyl, halogen, haloalkyl, optionally alkyl-, aryl- or aralkyl-substituted amino, denotes a heterocyclic radical, cyano, carboxyl, alkoxycarbonyl, hydroxyl or alkoxyl, the abovementioned organic radicals for R 1 each have 1 to 30 carbon atoms, and
  • n 0, 1 or 2
  • preferred compounds of this type include purine, adenine, 6-chloropurine, 2,6-dichloropurine, 6-methoxypurine, 1H-1, 2,3-triazolo (4,5B) pyridine, 6-histaminopurine and 6-furrarylaminopurine.
  • the borate-free DOT 4 brake fluids according to the invention can furthermore contain the formulations described in WO 02/081604 with 1H-1,2,4-triazole.
  • brake fluids according to the invention can contain the cyclic carboxylic acid derivatives of the general formula I listed in WO 00/65001
  • X represents an oxygen atom or a grouping of the formula NR 1 , where
  • R 1 denotes hydrogen or a linear or branched Q- to C 2 o-alkyl group, which can additionally be interrupted by up to 9 non-adjacent oxygen atoms and / or can carry up to 6 hydroxyl groups, or a cycloalkyl group or an optionally substituted phenyl group designated,
  • A denotes a grouping of the formula -CR 2 R 3 -, wherein
  • R and R represent hydrogen or C 1 -C 8 -alkyl groups, which can additionally be interrupted by up to 4 non-adjacent oxygen atoms and / or can carry up to 3 hydroxyl groups, and
  • n a number from 2 to 7. These are suitable as components for lowering the low-temperature viscosity in the presence of water.
  • components and auxiliaries in the brake fluids for motor vehicles according to the invention can include conventional antioxidants such as e.g. Phenothiazine and / or those based on phenol, and conventional defoamers and dyes.
  • the borate-free DOT 4 brake fluids according to the invention excellently meet the requirements mentioned at the outset and also have a generally good corrosion behavior compared to the prior art, i.e. Excellent protection against corrosion is achieved with metals such as iron, steel, tinplate, cast iron (gray cast iron), lead, tin, chromium, zinc, aluminum, magnesium and their alloys and with soldering metals, for example solder, as well as with non-ferrous metals such as copper and their alloys, for example Brass.
  • metals such as iron, steel, tinplate, cast iron (gray cast iron), lead, tin, chromium, zinc, aluminum, magnesium and their alloys and with soldering metals, for example solder, as well as with non-ferrous metals such as copper and their alloys, for example Brass.
  • DOT 4 brake fluids for motor vehicles are their favorable low-temperature viscosity, good water compatibility, a gentle pH value, good low-temperature, high-temperature and oxidation stability and good chemical stability, to emphasize favorable behavior (ie good compatibility) towards materials such as rubbers, plastics, glue joints, fiber, elastomer and rubber seals and similar materials as well as good lubricating behavior.
  • the borate-free DOT 4 brake fluid BF1 used according to the invention had the following composition:
  • Example BF 1 According to the Invention:
  • Comparative example BF 2 (corresponds to example 5 from DE 36 27 432 C2) 39% diethylene glycol
  • 1% corrosion inhibitor (used: l, l'-iminodipropan-2-ol)
  • the borate-free DOT 4 brake fluids according to the invention are distinguished from the prior art according to DE 3627432 C2 in particular by a significantly higher dry boiling point “ERBP”, which in BF 1 exceeds the minimum requirement according to FMVSS No. 116 by a good 20 ° C., and by a lower water absorption and associated higher wet boiling point "wet ERBP".
  • the brake fluids according to the invention also lead to very good corrosion protection, as the following results for BF 1 show:

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Braking Arrangements (AREA)

Abstract

The invention relates to a brake fluid that comprises a) 10 to 50 % by weight, preferably 20 to 40 % by weight, of diethylene glycol and/or dipropylene glycol, b) 50 to 90 % by weight, preferably 60 to 80 % by weight, of one or more monoalkylethers of (poly)ethylene glycol and/or (poly)propylene glycol. The inventive fluids are especially borate-free and owing to their low hygroscopicity are suitable for use in areas with high atmospheric humidity.

Description

DOT 4-Bremsflüssigkeiten DOT 4 brake fluids
Die vorliegende Erfindung betrifft neue DOT 4-Bremsflüssigkeiten, bei denen der Zusatz von Boraten (Borsäureestern) nicht notwendig ist. Die Bremsflüssigkeiten enthaltenThe present invention relates to new DOT 4 brake fluids in which the addition of borates (boric acid esters) is not necessary. The brake fluids included
(a) 10 bis 50 Gew.-% Diethylenglykol und/oder Dipropylenglykol und(a) 10 to 50% by weight of diethylene glycol and / or dipropylene glycol and
(b) 50 bis 90 Gew.-% (Poly)Ethylen- und/oder (Poly)Propylenglykolmonoalkylether(b) 50 to 90% by weight of (poly) ethylene and / or (poly) propylene glycol monoalkyl ether
und sind vorzugsweise frei von Polyglykoldialkylethern.and are preferably free of polyglycol dialkyl ethers.
Hydraulische Flüssigkeiten und insbesondere Bremsflüssigkeiten für Kraftfahrzeuge unterliegen hinsichtlich ihrer chemischen und physikalischen Eigenschaften sehr hohen Anfor- derangen. Entsprechend der bestehenden Normen und Spezifikationen für Bremsflüssigkeiten vom US-Department of Transportation (DOT) im Federal Motor Vehicle Saftey Standard FMVSS-Nr. 116 und der von der Society of Automotive Engineers herausgegebenen Norm SAE J 1704 sollen moderne Bremsflüssigkeiten einerseits über hohe Trockenkochpunkte (Rückflusssiedepunkte, trocken [Equilibrium reflux boiling point, „ERBP"]) sowie hohe Nasskochpunkte (Rückflussiedepunkte, feucht [„wet ERBP"]) verfügen, andererseits aber auch eine Viskosität aufweisen, die sich innerhalb eines weiten Temperaturbereiches nur wenig ändert.Hydraulic fluids and in particular brake fluids for motor vehicles are subject to very high requirements with regard to their chemical and physical properties. According to the existing standards and specifications for brake fluids from the US Department of Transportation (DOT) in the Federal Motor Vehicle Saftey Standard FMVSS-No. 116 and the SAE J 1704 standard published by the Society of Automotive Engineers, modern brake fluids are said to have high dry boiling points (reflux boiling points, dry [Equilibrium reflux boiling point, "ERBP"]) and high wet boiling points (reflux boiling points, moist ["wet ERBP"]) have, on the other hand, but also have a viscosity that changes only slightly within a wide temperature range.
Für eine DOT 4-Bremsflüssigkeit gemäß FMVSS-Nr. 116 müssen demnach die nachfol- gend aufgeführten Spezifikationswerte eingehalten werden:For a DOT 4 brake fluid according to FMVSS no. 116 the specification values listed below must therefore be observed:
Trockenkochpunkt „ERBP": > 230°CDry boiling point "ERBP":> 230 ° C
Nasskochpunkt „wet ERBP": > 155°C Viskosität bei -40°C: < 1800 mm2/sWet boiling point "wet ERBP":> 155 ° C viscosity at -40 ° C: <1800 mm 2 / s
Darüber hinaus bestehen weitergehende Anforderungen nach einem ausreichend guten Korrosionsschutz für Metalle und Buntmetalle durch Bremsflüssigkeiten, was durch darin enthaltene Korrosionsschutzadditive erreicht werden kann.In addition, there are further requirements for a sufficiently good corrosion protection for metals and non-ferrous metals by brake fluids, which can be achieved by the corrosion protection additives contained therein.
Marktübliche DOT 4-Bremsf üssigkeiten enthalten immer Borsäureester wie beispielsweise Methyltriglykolborat, die eindringendes Wasser in bestimmten Mengen aus der Bremsflüssigkeit durch Hydrolyse chemisch eliminieren können. Nachteilig dabei ist, dass Borsäureester selbst hygroskopisch sind, wodurch solche DOT 4-Bremsflüssigkeiten insbesondere in Regionen mit hoher Luftfeuchtigkeit, beispielsweise in tropischen und subtropi- schen Gebieten sehr schnell so viel Feuchtigkeit aufnehmen können, dass trotz Auffangfunktion der Borsäureester die Funktionsfähigkeit eines damit gefüllten Bremssystems negativ beeinträchtigt werden kann.Commercial DOT 4 brake fluids always contain boric acid esters such as methyl triglycol borate, which can chemically eliminate penetrating water from the brake fluid in certain quantities by hydrolysis. The disadvantage here is that boric acid esters themselves are hygroscopic, which means that such DOT 4 brake fluids are particularly useful in regions with high air humidity, for example in tropical and subtropical regions. areas can absorb so much moisture very quickly that the functionality of a brake system filled with it can be adversely affected despite the boric acid ester's collection function.
In der US 3,625, 899 werden DOT 4-Bremsflüssigkeiten beschrieben, welche 54,5 bis 92% wenigstens eines Borsäureesters, bis zu 20% Polyalkylenglykole und 3 bis 43% Polygly- kolmonoalkyl- oder -dialkylether neben weiteren Additiven enthalten.US Pat. No. 3,625,899 describes DOT 4 brake fluids which contain 54.5 to 92% of at least one boric acid ester, up to 20% polyalkylene glycols and 3 to 43% polyglycol monoalkyl or dialkyl ether in addition to other additives.
Die US 3,972, 822 beschreibt DOT 4-Bremsflüssigkeiten welche 40 bis 65% Polyglykol- monoalkylether, 16 bis 45% Polyglykole und 10 bis 19% Borsäureester plus Korrosionsin- bibitoren enthalten.No. 3,972,822 describes DOT 4 brake fluids which contain 40 to 65% polyglycol monoalkyl ether, 16 to 45% polyglycols and 10 to 19% boric acid ester plus corrosion inhibitors.
In der WO 00/46325 werden DOT 4-Bremsflüssigkeiten beschrieben, die Methyltriglykol- borat, Glykolether und Glykole in unterschiedlichen Mengen sowie ein Additivsystem ent- halten.WO 00/46325 describes DOT 4 brake fluids which contain methyl triglycol borate, glycol ethers and glycols in different amounts and an additive system.
Auch in der WO 02/38711 werden entsprechende DOT 4-Bremsflüssigkeiten offenbart, die unterschiedliche Methylpolyglykolborate, Polyglykolmonoalkylether sowie Korrosionsin- hibitoren enthalten.Corresponding DOT 4 brake fluids are also disclosed in WO 02/38711, which contain different methylpolyglycol borates, polyglycol monoalkyl ethers and corrosion inhibitors.
In der DE 36 27 432 C2 werden boratfreie Bremsflüssigkeiten von 30 bis 80% einer Gly- kolkomponente und bis 70% Polyglykolalkylethern beschrieben. Die Glykolkomponente wiederum enthält 0 bis 80 Gew.-%, vorzugsweise 55 bis 80 Gew.-% Diethylenglykol und/oder Dipropylenglykol. Die Polyglykolalkylether-Komponente enthält 0 bis 90 Gew.- % vorzugsweise 0 bis 50 Gew.-% mindestens eines Polyglykolmonoalkylether s. Diese Flüssigkeiten erfüllen in ausgewählten Mischungsverhältnissen die DOT 4-Spezifikation. Nachteilig ist bei diesem Formulierungen insbesondere der nur knapp oberhalb der Spezifikationsgrenze liegende Trockenkochpunkt „ERBP" und außerdem der Einsatz von aufwendiger zu synthetisierenden Polyglykoldialkylethern, die oft auch zu Unverträglichkeits- reaktionen von Gummi- und Dichtungsmaterialien führen.DE 36 27 432 C2 describes borate-free brake fluids of 30 to 80% of a glycol component and up to 70% polyglycol alkyl ethers. The glycol component in turn contains 0 to 80% by weight, preferably 55 to 80% by weight, of diethylene glycol and / or dipropylene glycol. The polyglycol alkyl ether component contains 0 to 90% by weight, preferably 0 to 50% by weight, of at least one polyglycol monoalkyl ether. These liquids meet the DOT 4 specification in selected mixing ratios. A disadvantage of these formulations is, in particular, the dry boiling point “ERBP”, which is just above the specification limit, and also the use of complex polyglycol dialkyl ethers which are difficult to synthesize and which often also lead to incompatibility reactions of rubber and sealing materials.
Es besteht weiterhin ein Bedarf an niedrigviskosen Bremsflüssigkeiten, die die DOT 4- Spezifikation erfüllen.There is still a need for low viscosity brake fluids that meet the DOT 4 specification.
Die Aufgabe der vorliegenden Erfindung besteht in der Bereitstellung einer solchen Bremsflüssigkeit. Vorzugsweise soll diese Bremsflüssigkeit wenig hygroskopisch und in Regionen mit hoher Luftfeuchtigkeit einsetzbar sein. Insbesondere soll der Umsatz nur noch geringe Mengen Borsäureester notwendig oder im Idealfall sogar gänzlich überflüssig sein. Diese Aufgabe wird gelöst durch eine Bremsflüssigkeit enthaltendThe object of the present invention is to provide such a brake fluid. This brake fluid should preferably be less hygroscopic and usable in regions with high air humidity. In particular, the conversion should only require small amounts of boric acid esters or, ideally, even be completely unnecessary. This object is achieved by containing a brake fluid
a) 10 bis 50 Gew.-% Diethylenglykol und/oder Dipropylenglykol und b) 50 bis 90 Gew.-% einen oder mehrere Monoalkylether von (Poly)Ethylenglykol oder (Poly)Propylenglykol.a) 10 to 50% by weight of diethylene glycol and / or dipropylene glycol and b) 50 to 90% by weight of one or more monoalkyl ethers of (poly) ethylene glycol or (poly) propylene glycol.
Insbesondere sind die erfindungsgemäßen Flüssigkeiten frei von Borsäureestern.In particular, the liquids according to the invention are free from boric acid esters.
Es kann Diethylenglykol oder Dipropylenglykol oder eine Mischung von Diethylenglykol und Dipropylenglykol in einem beliebigen Verhältnis eingesetzt werden. Bevorzugt ist Diethylenglykol.Diethylene glycol or dipropylene glycol or a mixture of diethylene glycol and dipropylene glycol can be used in any ratio. Diethylene glycol is preferred.
Diethylenglykol und/oder Dipropylenglykol sind in den erfindungsgemäßen Bremsflüssigkeiten in einer Menge von 10 bis 50 Gew.-%, vorzugsweise 20 bis 40 Gew.-% vorhanden.Diethylene glycol and / or dipropylene glycol are present in the brake fluids according to the invention in an amount of 10 to 50% by weight, preferably 20 to 40% by weight.
Eine weitere Komponente der erfindungsgemäßen Bremsflüssigkeiten sind ein oder mehrere Monoalkylether von (Poly)Ethylenglykolen und/oder (Poly)Propylenglykolen, die in den erfindungsgemäßen Flüssigkeiten in einer Menge von 50 bis 90 Gew.-%, vorzugsweise 60 bis 80 Gew.-%, vorhanden sind. .Another component of the brake fluids according to the invention are one or more monoalkyl ethers of (poly) ethylene glycols and / or (poly) propylene glycols, which are present in the fluids according to the invention in an amount of 50 to 90% by weight, preferably 60 to 80% by weight, available. ,
Beispiele für geeignete (Poly)Ethylenglykole sind Monoethylenglykol, Diethylenglykol, Triethylenglykol, Tetraethylenglykol, Pentaethylenglykol und Hexaethylenglykol.Examples of suitable (poly) ethylene glycols are monoethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, pentaethylene glycol and hexaethylene glycol.
Beispiele für geeignete (Poly)Propylenglykole sind Monopropylenglykol, Dipropylengly- kol, Tripropylenglykol, Tetrapropylenglykol, Pentapropylenglykol und Hexapropylengly- kol.Examples of suitable (poly) propylene glycols are monopropylene glycol, dipropylene glycol, tripropylene glycol, tetrapropylene glycol, pentapropylene glycol and hexapropylene glycol.
Bevorzugt sind Diethylenglykol, Triethylenglykol und/oder Tetraethylenglykol.Diethylene glycol, triethylene glycol and / or tetraethylene glycol are preferred.
Der Alkylrest in den erfindungsgemäß eingesetzten Monoalkylethern von (Po- ly)Ethylenglykol und (Poly)Propylenglykol ist vorzugsweise ein linearer oder verzweigter - - Alkylrest. Es ist mehr bevorzugt, einen linearen oder verzweigten -C4- Alkylrest einzusetzen, beispielsweise Methyl, Ethyl, i-Propyl, n-Propyl, n-Butyl, i-Butyl, sec-Butyl oder tert-Butyl.The alkyl radical in the monoalkyl ethers of (poly) ethylene glycol and (poly) propylene glycol used according to the invention is preferably a linear or branched - - alkyl radical. It is more preferred to use a linear or branched C4-alkyl radical, for example methyl, ethyl, i-propyl, n-propyl, n-butyl, i-butyl, sec-butyl or tert-butyl.
Insbesondere sind die Alkylreste Methyl, Ethyl, i-Propyl oder n-Butyl. Im Rahmen der vorliegenden Erfindung ist der Einsatz von Methyldiethylenglykol, Me- thyltriethylenglykol, Methyltetraethylenglykol und oder Butyltriethylenglykol bevorzugt.In particular, the alkyl radicals are methyl, ethyl, i-propyl or n-butyl. In the context of the present invention, the use of methyldiethylene glycol, methyltriethylene glycol, methyltetraethylene glycol and or butyltriethylene glycol is preferred.
Die erfindungsgemäßen Bremsflüssigkeiten weisen Nasskochpunkte und insbesondere Trockenkochpunkte auf, die bei denen liegen, die bisher mit boratfreien Bremsflüssigkeiten erzielt werden konnten. Sie sind mit denen vergleichbar, die bislang nur mit borathaltigen Flüssigkeiten erzielt wurden. Durch die Abwesenheit von Borat sind die erfindungsgemäßen Flüssigkeiten jedoch deutlich weniger hygroskopisch als borathaltige. Dies ist insbesondere beim Einsatz in tropischen und subtropischen Gebieten vorteilhaft, da durch den Boratzusatz zwar ein Teil des Wassers gebunden wird, jedoch relativ schnell auch Wasser aufgenommen wird. Dadurch tritt in jedem Fall eine Qualitätsverschlechterung der Bremsflüssigkeit ein. Insbesondere tritt dieser Qualitätsverlust häufig häufig im Bremssystem von Kraftfahrzeugen, aber auch bereits bei Lagerung und Transport der Flüssigkeiten ein. Die erfindungsgemäßen Bremsflüssigkeiten weisen die genannten Nachteile nicht auf.The brake fluids according to the invention have wet boiling points and, in particular, dry boiling points which are those which have hitherto been achieved with borate-free brake fluids. They are comparable to those that have so far only been achieved with liquids containing borate. Due to the absence of borate, the liquids according to the invention are significantly less hygroscopic than those containing borate. This is particularly advantageous when used in tropical and subtropical areas, since part of the water is bound by the addition of borate, but water is also absorbed relatively quickly. This results in a deterioration in the quality of the brake fluid. In particular, this loss of quality often occurs in the braking system of motor vehicles, but also during the storage and transportation of the liquids. The brake fluids according to the invention do not have the disadvantages mentioned.
Die erfindungsgemäßen Bremsflüssigkeiten können zwar Borsäureestern in unterschiedlichen Mengen enthalten. Jedoch werden damit die erfindungsgemäßen Vorteile der geringen Hygroskopizität im allgemeinen nicht erreicht. Dies ist insbesondere dann der Fall, wenn die bisher nach dem Stand der Technik üblichen Mengen an Borsäurestern zugegeben wer- den.The brake fluids according to the invention can contain boric acid esters in different amounts. However, the advantages of low hygroscopicity according to the invention are generally not achieved in this way. This is especially the case when the amounts of boric acid esters customary according to the prior art are added.
Weiterhin sind die erfindungsgemäßen Flüssigkeiten insbesondere frei von Polyalkylengly- koldialkylethern. Auch diese können zwar in unterschiedlichen Mengen enthalten sein, jedoch werden dann im allgemeinen die Vorteile der erfindungsgemäßen Bremsflüssigkei- ten, insbesondere die Verträglichkeit mit Gummi- und Dichtungsmaterialien, nicht erreicht, wobei dies auch hier natürlich von der Menge der eventuell vorhandenen Polyalkylengly- koldialkylether abhängt.Furthermore, the liquids according to the invention are in particular free from polyalkylene glycol dialkyl ethers. Although these may also be present in different amounts, the advantages of the brake fluids according to the invention, in particular the compatibility with rubber and sealing materials, are generally not achieved, this of course also depending on the amount of polyalkylene glycol dialkyl ethers that may be present ,
Als optionale Komponente können weitere Polyglykole in den erfindungsgemäßen Formu- lierangen enthalten sein. Dabei werden vorzugsweise höhersiedende Umsetzungsprodukte von Ethylenoxid und/oder Propylenoxid und/oder Butylenoxid mit Wasser oder Diolen eingesetzt. Insbesondere finden Umsetzungsprodukte von Gemischen aus Ethylenoxid und Propylenoxid mit Wasser Verwendung. Die Anzahl der Alkylenoxid-Einheiten in den genannten Polyglykolen beträgt normalerweise generell 2 bis 10, vorzugsweise 2 bis 3 und in einer Menge von bis zu 5 %.Further polyglycols can be contained in the formulation bars according to the invention as an optional component. Higher-boiling reaction products of ethylene oxide and / or propylene oxide and / or butylene oxide with water or diols are preferably used. In particular, reaction products of mixtures of ethylene oxide and propylene oxide with water are used. The number of alkylene oxide units in the polyglycols mentioned is generally 2 to 10, preferably 2 to 3 and in an amount of up to 5%.
Die Wirkung dieser hochsiedenden Polyglykole ist die eines Sclimierrriittels, was im wesentlichen auf eine Verbesserung des Temperatur- Viskositäts-Verhaltens zurückzuführen ist. Die Polyglykole verleihen den bei hohen Temperaturen oftmals dünnflüssigen Polygly- kolmonoalkylethern genügend Viskosität und sorgen damit für eine ausreichende Schmierung. Eine genügende Schmierung ist erwünscht, da in den Bauteilen des Kraftfahrzeug- Bremssystems Gummi oder Elastomere auf Metall möglichst verschleißfrei gleiten müssen.The effect of these high-boiling polyglycols is that of a reducing agent, which is essentially due to an improvement in the temperature-viscosity behavior. The polyglycols give the polyglycols, which are often thin at high temperatures, colmonoalkyl ethers have sufficient viscosity and thus ensure adequate lubrication. Adequate lubrication is desirable since rubber or elastomers on metal in the components of the motor vehicle brake system must slide as wear-free as possible.
In einer weiteren Ausführangsform enthalten die erfindungsgemäßen DOT 4-In a further embodiment, the DOT 4- according to the invention contain
Bremsflüssigkeiten für Kraftfahrzeuge, weiterhin 0,001 bis 10 Gew.-%, vorzugsweise 0,005 bis 4 Gew.-%5 insbesondere 0,005 bis 1 Gew.-%, eines oder mehrerer Korrosionsinhibitoren, beispielsweise lH-l,2,3-Benzotriazol, lH-l,2,3-Tolutriazol, hydriertes 1H-1,2,3- Tolutriazol, Benzimidazol und/oder deren Derivate, Alkalimetallsalze von Phosphorsäure und phosphoriger Säure, Fettsäuren, vorzugsweise Capryl-, Laurin-, Palmitin-, Stearinoder Ölsäure sowie deren Alkalimetallsalze, Ester der Phosphorsäure und der phosphorigen Säure, vorzugsweise Ethylphosphat, Dimethylphosphat, Isopropylphosphat, Disopro- pylphosphat, Butyiphosphit oder Dimethylphosphit, gegebenenfalls ethoxylierte Mono- und Dialkylamine und deren Salze mit Mineral- und Fettsäuren, vorzugsweise Butylamin, Hexylamin, Octylamin, Isononylamin, Oleylamin, Dipropylamin, Diisopropylamin oder Dibutylamin, gegebenenfalls ethoxylierte Alkanolamine, vorzugsweise Mono-, Di-, oder Triethanolamin, N,N'-Di-n-Butylaminoethanol oder l,l'-Iminodipropan-2-ol, Cyclohexy- lamin, und/oder Nitroaromaten, vorzugsweise 3-Nitrobenzaldehyd.Brake fluids for motor vehicles, further 0.001 to 10% by weight, preferably 0.005 to 4% by weight 5, in particular 0.005 to 1% by weight, of one or more corrosion inhibitors, for example 1H-1, 2,3-benzotriazole, 1H-1 , 2,3-tolutriazole, hydrogenated 1H-1,2,3-tolutriazole, benzimidazole and / or their derivatives, alkali metal salts of phosphoric acid and phosphorous acid, fatty acids, preferably caprylic, lauric, palmitic, stearic or oleic acid and their alkali metal salts, Esters of phosphoric acid and phosphorous acid, preferably ethyl phosphate, dimethyl phosphate, isopropyl phosphate, disopropyl phosphate, butyiphosphite or dimethyl phosphite, optionally ethoxylated mono- and dialkylamines and their salts with mineral and fatty acids, preferably butylamine, hexylamine, octylamine, isononylamine, oleylamine, oleylamine , Diisopropylamine or dibutylamine, optionally ethoxylated alkanolamines, preferably mono-, di- or triethanolamine, N, N'-di-n-butylaminoethanol or l , l'-Iminodipropan-2-ol, cyclohexyl laminate, and / or nitroaromatics, preferably 3-nitrobenzaldehyde.
Auch eine oder mehrere der in WO 01/90281 beschriebenen heterocyclischen Verbindungen der nachstehenden allgemeinen FormelAlso one or more of the heterocyclic compounds of the following general formula described in WO 01/90281
Figure imgf000006_0001
Figure imgf000006_0001
in derin the
(i) x für N, Y für CR und Z für N oder(i) x for N, Y for CR and Z for N or
(ii) X für N, Y für N und Z für N oder CR oder(ii) X for N, Y for N and Z for N or CR or
(iii) X für CR, Y für N und Z für N steht,(iii) X is CR, Y is N and Z is N,
wobeiin which
R, jeweils unabhängig von weiteren vorhandenen Resten R, ein Wasserstoff atom oder einen Rest R1 bezeichnet, R1, jeweils unabhängig von weiteren vorhandenen Resten R1, Alkyl, Aryl, Aralkyl, Halogen, Halogenalkyl, gegebenenfalls alkyl-, aryl- oder aralkylsubstituiertes Amino, einen heterocychschen Rest, Cyano, Carboxyl, Alkoxycarbonyl, Hydroxyl oder Alkoxyl bedeutet, wobei die genannten organischen Reste für R1 jeweils 1 bis 30 C- Atome aufweisen, undR, atom in each case independently of other radicals R present, a hydrogen or denotes a radical R 1, R 1 , each independently of other radicals R 1 , alkyl, aryl, aralkyl, halogen, haloalkyl, optionally alkyl-, aryl- or aralkyl-substituted amino, denotes a heterocyclic radical, cyano, carboxyl, alkoxycarbonyl, hydroxyl or alkoxyl, the abovementioned organic radicals for R 1 each have 1 to 30 carbon atoms, and
n für 0, 1 oder 2 steht, können in den erfindungsgemäßen Bremsflüssigkeiten enthalten sein. Beispiele für bevorzugte Verbindungen dieses Typs umfassen Purin, Adenin, 6- Chloropurin, 2,6-Dichloropurin, 6-Methoxypurin, lH-l,2,3-Triazolo(4,5B)pyridin, 6- Histaminopurin und 6-Furrarylaminopurin.n stands for 0, 1 or 2, can be contained in the brake fluids according to the invention. Examples of preferred compounds of this type include purine, adenine, 6-chloropurine, 2,6-dichloropurine, 6-methoxypurine, 1H-1, 2,3-triazolo (4,5B) pyridine, 6-histaminopurine and 6-furrarylaminopurine.
Die erfindungemäßen boratfreien DOT 4-Bremsflüssigkeiten können weiterhin die in WO 02/081604 beschriebenen Formulierungen mit lH-l,2,4-Triazol enthalten.The borate-free DOT 4 brake fluids according to the invention can furthermore contain the formulations described in WO 02/081604 with 1H-1,2,4-triazole.
Außerdem können die erfindungsgemäßen Bremsflüssigkeiten die in WO 00/65001 aufge- führten cyclischen Carbonsäurederivate der allgemeinen Formel IIn addition, the brake fluids according to the invention can contain the cyclic carboxylic acid derivatives of the general formula I listed in WO 00/65001
Figure imgf000007_0001
Figure imgf000007_0001
enthalten, in derincluded in the
X für ein Sauerstoffatom oder eine Gruppierung der Formel N-R1 steht, wobeiX represents an oxygen atom or a grouping of the formula NR 1 , where
R1 Wasserstoff oder eine lineare oder verzweigte Q- bis C2o-Alkylgrappe bezeichnet, welche noch zusätzlich durch bis zu 9 nicht benachbarte Sauerstoffatome unterbrochen sein und/oder bis zu 6 Hydroxylgruppen tragen kann, oder eine Cycloalkylgrup- pe oder eine gegebenenfalls substituierte Phenylgrappe bezeichnet,R 1 denotes hydrogen or a linear or branched Q- to C 2 o-alkyl group, which can additionally be interrupted by up to 9 non-adjacent oxygen atoms and / or can carry up to 6 hydroxyl groups, or a cycloalkyl group or an optionally substituted phenyl group designated,
A eine Gruppierung der Formel -CR2R3- bezeichnet, wobeiA denotes a grouping of the formula -CR 2 R 3 -, wherein
R und R für Wasserstoff oder Ci- bis C8-Alkylgruppen stehen, welche noch zusätzlich durch bis zu 4 nicht benachbarte Sauerstoffatome unterbrochen sein und/oder bis zu 3 Hydroxylgruppen tragen können, undR and R represent hydrogen or C 1 -C 8 -alkyl groups, which can additionally be interrupted by up to 4 non-adjacent oxygen atoms and / or can carry up to 3 hydroxyl groups, and
n eine Zahl von 2 bis 7 bedeutet. Diese sind als Komponenten zur Erniedrigung der Tieftemperaturviskosität in Anwesenheit von Wasser geeignet.n represents a number from 2 to 7. These are suitable as components for lowering the low-temperature viscosity in the presence of water.
Weitere Komponenten und Hilfsmittel in den erfindungsgemäßen Bremsflüssigkeiten für Kraftfahrzeuge können übliche Antioxidationsmittel wie z.B. Phenothiazin und/solche auf Phenolbasis, und übliche Entschäumer sowie Farbstoffe sein.Other components and auxiliaries in the brake fluids for motor vehicles according to the invention can include conventional antioxidants such as e.g. Phenothiazine and / or those based on phenol, and conventional defoamers and dyes.
Alle vorstehenden und nachfolgenden Gew.-%- Angaben beziehen sich jeweils auf die Gesamtmenge der hydraulischen Flüssigkeit bzw. der Bremsflüssigkeit.All of the above and following percentages by weight relate to the total amount of hydraulic fluid or brake fluid.
Die erfindungsgemäßen boratfreien DOT 4-Bremsflüssigkeiten werden in hervorragender Weise den eingangs genannten Anforderungen gerecht und weisen außerdem einen gegenüber dem Stand der Technik generell gutes Korrosionsverhalten auf, d.h. ein sehr guter Korrosionsschutz wird bei Metallen wie Eisen, Stahl, Weißblech, Gusseisen (Grauguss), Blei, Zinn, Chrom, Zink, Aluminium, Magnesium und deren Legierungen und bei Lötmetallen, beispielsweise Lötzinn, sowie bei Buntmetallen wie Kupfer und deren Legierungen, beispielsweise Messing, bewirkt.The borate-free DOT 4 brake fluids according to the invention excellently meet the requirements mentioned at the outset and also have a generally good corrosion behavior compared to the prior art, i.e. Excellent protection against corrosion is achieved with metals such as iron, steel, tinplate, cast iron (gray cast iron), lead, tin, chromium, zinc, aluminum, magnesium and their alloys and with soldering metals, for example solder, as well as with non-ferrous metals such as copper and their alloys, for example Brass.
Neben den durch die Boratfreiheit deutlich verringerten hygroskopischen Eigenschaften sind als weitere Vorteile der erfindungsgemäßen DOT 4-Bremsflüssigkeiten für Kraftfahrzeuge deren günstige Tieftemperaturviskosität, eine gute Wasserverträglichkeit, ein schonender pH- Wert, eine gute Kälte-, Hochtemperatur- und Oxidationsstabilität sowie eine gute chemische Stabilität, ein günstiges Verhalten (d.h. eine gute Verträglichkeit) gegenüber Werkstoffen wie Kautschuken, Kunststoffen, Leimfugen, Fiber-, Elastomeren- und Gummidichtungen und ähnlichen Materialien sowie ein gutes Schmierverhalten hervorzuheben.In addition to the hygroscopic properties which are significantly reduced by the absence of borate, further advantages of the DOT 4 brake fluids for motor vehicles according to the invention are their favorable low-temperature viscosity, good water compatibility, a gentle pH value, good low-temperature, high-temperature and oxidation stability and good chemical stability, to emphasize favorable behavior (ie good compatibility) towards materials such as rubbers, plastics, glue joints, fiber, elastomer and rubber seals and similar materials as well as good lubricating behavior.
Die nachfolgenden Beispiele sollen die vorliegende Erfindung erläutern, ohne sie zu beschränken.The following examples are intended to illustrate the present invention without restricting it.
Anwendungstechnische Beispiele:Application examples:
Die verwendete erfindungsgemäße boratfreie DOT 4-Bremsflüssigkeit BF1 hatte folgende Zusammensetzung:The borate-free DOT 4 brake fluid BF1 used according to the invention had the following composition:
Erfindungsgemäßes Beispiel BF 1:Example BF 1 According to the Invention:
31 ,0 % Diethylenglykol 67,7 % Mischung aus Methyldiglykol, Butyldiglykol, Butyltriglykol u. Methyltetragly- kol 1,3 % Mischung aus l, -Iminodipropan-2-ol, Bisphenol A, Tolutriazol u. 3-31.0% diethylene glycol 67.7% mixture of methyl diglycol, butyl diglycol, butyl triglycol and. Methyl tetraglycol 1.3% mixture of l, -Iminodipropan-2-ol, bisphenol A, tolutriazole and. 3
Nitrobenzaldehydnitrobenzaldehyde
Vergleichsbeispiel BF 2 (entspricht Beispiel 5 aus DE 36 27 432 C2) 39 % DiethylenglykolComparative example BF 2 (corresponds to example 5 from DE 36 27 432 C2) 39% diethylene glycol
26 % Triethylenglykol 24 % Triethylenglykoldimethylether26% triethylene glycol 24% triethylene glycol dimethyl ether
10 % Methyltriglykol10% methyl triglycol
1 % Korrosionsinhibitor (verwendet: l,l'-Iminodipropan-2-ol)1% corrosion inhibitor (used: l, l'-iminodipropan-2-ol)
Physikalische Daten: BF 1 BF 2 (Vergleich)Physical data: BF 1 BF 2 (comparison)
ERBP [°C]: 251 234 wet ERBP [°C]: 159 153ERBP [° C]: 251 234 wet ERBP [° C]: 159 153
(Wasseraufnahme: (Wasseraufnahme:(Water intake: (Water intake:
3,27 %; Referenz RM 71 3,73 % ) 3,93%; Referenz RM 71 3,70%) Viskosität -40 °C: 1393 12773.27%; Reference RM 71 3.73%) 3.93%; Reference RM 71 3.70%) Viscosity -40 ° C: 1393 1277
[mm2/s][mm 2 / s]
Die erfindungsgemäßen boratfreien DOT 4-Bremsflüssigkeiten zeichnen sich gegenüber dem Stand der Technik gemäß DE 3627432 C2 insbesondere durch einen deutlich höheren Trockensiedepunkt „ERBP" aus, der bei BF 1 die Mindestanforderung gemäß FMVSS Nr. 116 um gut 20°C überschreitet, sowie durch eine geringere Wasseraufnahme und damit verbundenen höheren Nasskochpunkt „wet ERBP". Die erfindungsgemäßen Bremsflüssigkeiten führen außerdem zu einem sehr guten Korrosionsschutz, wie die nachstehenden Ergebnisse für BF 1 zeigen:The borate-free DOT 4 brake fluids according to the invention are distinguished from the prior art according to DE 3627432 C2 in particular by a significantly higher dry boiling point “ERBP”, which in BF 1 exceeds the minimum requirement according to FMVSS No. 116 by a good 20 ° C., and by a lower water absorption and associated higher wet boiling point "wet ERBP". The brake fluids according to the invention also lead to very good corrosion protection, as the following results for BF 1 show:
Korrosionstest gemäß SAE J 1704, Testdauer 120h/100 °C:Corrosion test according to SAE J 1704, test duration 120h / 100 ° C:
Metall Gewichtsänderang Aussehen [mg/cm2]Metal weight change appearance [mg / cm 2 ]
Weißblech ±0,00 unverändertTinplate ± 0.00 unchanged
Stahl +0,01 unverändert Aluminium ±0,00 unverändertSteel + 0.01 unchanged Aluminum ± 0.00 unchanged
Grauguss +0,04 unverändertGray cast iron +0.04 unchanged
Messing -0,05 leicht angelaufenBrass -0.05 slightly tarnished
Kupfer -0,05 leicht angelaufenCopper -0.05 slightly tarnished
Zink +0,03 angelaufenZinc +0.03 tarnished
pH- Wert vor / nach Test: 9,9 /9,6 pH before / after test: 9.9 / 9.6

Claims

Patentansprüche claims
1. Bremsflüssigkeit enthaltend a) 10 bis 50 Gew.-%, vorzugsweise 20 bis 40 Gew.-%, Diethylenglykol und /oder Dipropylenglykol b) 50 bis 90 Gew.-%, vorzugsweise 60 bis 80 Gew.-%, einen oder mehrere Monoalkylether von (Poly)Ethylenglykol und/oder (Poly)Propylenglykol.1. Brake fluid containing a) 10 to 50% by weight, preferably 20 to 40% by weight, diethylene glycol and / or dipropylene glycol b) 50 to 90% by weight, preferably 60 to 80% by weight, one or more Monoalkyl ether of (poly) ethylene glycol and / or (poly) propylene glycol.
2. Flüssigkeit nach Anspruch 1, dadurch gekennzeichnet, dass diese keine Borsäu- reester enthält.2. Liquid according to claim 1, characterized in that it contains no boric acid esters.
3. Flüssigkeit nach Ansprach 1 oder 2, dadurch gekennzeichnet, dass diese keine Po- lyalkylenglykoldialkylether enthält.3. Liquid according spoke 1 or 2, characterized in that it contains no polyalkylene glycol dialkyl ether.
4. Flüssigkeit nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass als4. Liquid according to one of claims 1 to 3, characterized in that as
Komponente a) Diethylenglykol verwendet wird.Component a) diethylene glycol is used.
5. Flüssigkeit nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, dass in der Komponente b) die Glykole ausgewählt sind aus Monoethylenglykol, Diethylengly- kol, Triethylenglykol, Tetraethylenglykol, Pentaethylenglykol, Hexaethylenglykol,5. Liquid according to one of claims 1 to 4, characterized in that in component b) the glycols are selected from monoethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, pentaethylene glycol, hexaethylene glycol,
Monopropylenglykol, Dipropylenglykol, Tripropylenglykol, Tetrapropylenglykol, Pentapropylenglykol und Hexapropylenglykol.Monopropylene glycol, dipropylene glycol, tripropylene glycol, tetrapropylene glycol, pentapropylene glycol and hexapropylene glycol.
6. Flüssigkeit nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, dass in der Komponente b) der Alkylrest ausgewählt ist aus linearen oder verzweigten Ci-C6-6. Liquid according to one of claims 1 to 5, characterized in that in component b) the alkyl radical is selected from linear or branched Ci-C 6 -
Alkylresten, vorzugsweise linearen und verzweigten C1-C4-Alkylresten, insbesondere Methyl, Ethyl, i-Propyl oder n-Butyl.Alkyl radicals, preferably linear and branched C 1 -C 4 alkyl radicals, in particular methyl, ethyl, i-propyl or n-butyl.
7. Flüssigkeit nach einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, dass die Komponente b) ausgewählt ist aus Methyldiethylenglykol, Methyltriethylenglykol,7. Liquid according to one of claims 1 to 6, characterized in that component b) is selected from methyldiethylene glycol, methyltriethylene glycol,
Methyltetraethylenglykol und Butyltriethylenglykol.Methyl tetraethylene glycol and butyltriethylene glycol.
8. Flüssigkeit nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, dass weiterhin Umsetzungsprodukte von Ethylenoxid und oder Propylenoxid und/oder Bu- tylenoxid mit Wasser oder Diolen, vorzugsweise Umsetzungsprodukte von Gemischen aus Ethylenoxid und Propylenoxid mit Wasser mit 2 bis 10, vorzugsweise 2 bis 3 Alkylenoxid-Einheiten vorhanden sind. 8. Liquid according to one of claims 1 to 7, characterized in that further reaction products of ethylene oxide and or propylene oxide and / or butylene oxide with water or diols, preferably reaction products of mixtures of ethylene oxide and propylene oxide with water with 2 to 10, preferably 2 up to 3 alkylene oxide units are present.
. Flüssigkeit nach einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, dass 0,01 bis 10 Gew.-%, vorzugsweise 0,005 bis 4 Gew.-%, insbesondere 0,005 bis 1 Gew.- %, eine oder mehrere Korrosionsinhibitoren vorhanden sind., Liquid according to one of claims 1 to 8, characterized in that 0.01 to 10 wt .-%, preferably 0.005 to 4 wt .-%, in particular 0.005 to 1 wt .-%, one or more corrosion inhibitors are present.
10. Flüssigkeit nach einem der Ansprüche 1 bis 9, dadurch gekennzeichnet, dass die10. Liquid according to one of claims 1 to 9, characterized in that the
Korrosionsinhibitoren ausgewählt sind aus der Gruppe lH-l,2,3-Benzotriazol, 1H- 1,2,3-Tolutriazol, hydriertes lH-l,2,3-Tolutriazol, Benzirnidazol und/oder deren Derivate, Alkalimetallsalze von Phosphorsäure und phosphoriger Säure, Fettsäuren, vorzugsweise Capryl-, Laurin-, Palmitin-, Stearin- oder Ölsäure und deren Alkali- metallsalze, Ester der Phosphorsäure und der phosphorigen Säure, vorzugsweiseCorrosion inhibitors are selected from the group 1H-1, 2,3-benzotriazole, 1H-1,2,3-tolutriazole, hydrogenated 1H-1, 2,3-tolutriazole, benzirnidazole and / or their derivatives, alkali metal salts of phosphoric acid and phosphorous acid , Fatty acids, preferably caprylic, lauric, palmitic, stearic or oleic acid and their alkali metal salts, esters of phosphoric acid and phosphorous acid, preferably
Ethylphosphat, Dimethylphosphat, Isopropylphosphat, Diisopropylphosphat, Butyl- phosphit oder Dimethylphosphit, gegebenenfalls ethoxylierte Mono- und Dialkyla- mine und deren Salze mit Mineral- und Fettsäuren, vorzugsweise Butylamin, Hexylamin, Octylamin, Isononylamin, Oleylamin, Dipropylamin, Diisopropylamin oder Dibutylamin, gegebenenfalls ethoxylierte Alkanolamine, vorzugsweise Mono-, Di-, oder Triethanolamin, N,N'-Di-n-Butylaminoethanol oder l, -Iminodipropan-2-ol, Cyclohexylamin, und/oder Nitroaromaten, vorzugsweise 3-Nitrobenzaldehyd.Ethyl phosphate, dimethyl phosphate, isopropyl phosphate, diisopropyl phosphate, butyl phosphite or dimethyl phosphite, optionally ethoxylated mono- and dialkylamines and their salts with mineral and fatty acids, preferably butylamine, hexylamine, octylamine, isononylamine, oleylamine, dipropylamine, diutopropylamine, optionally ethoxylated amine or diisopropylamine Alkanolamines, preferably mono-, di- or triethanolamine, N, N'-di-n-butylaminoethanol or l, -iminodipropan-2-ol, cyclohexylamine, and / or nitroaromatics, preferably 3-nitrobenzaldehyde.
11. Flüssigkeit nach einem der Ansprüche 1 bis 10, dadurch gekennzeichnet, dass diese die folgenden Spezifikationswerte (DOT 4) einhält:11. Liquid according to one of claims 1 to 10, characterized in that it meets the following specification values (DOT 4):
Trockenkochpunkt „ERBP": > 230°CDry boiling point "ERBP":> 230 ° C
Nasskochpunkt „wet ERBP": > 155°CWet boiling point "wet ERBP":> 155 ° C
Viskosität bei -40°C: < 1800mm2/sViscosity at -40 ° C: <1800mm 2 / s
12. Verwendung einer Flüssigkeit nach einem der Ansprüche 1 bis 11 als Bremsflüssigkeit in Kraftfahrzeugen, vorzugsweise in Gebieten mit hoher Luftfeuchtigkeit. 12. Use of a liquid according to one of claims 1 to 11 as a brake fluid in motor vehicles, preferably in areas with high humidity.
PCT/EP2004/002552 2003-03-12 2004-03-11 Dot 4 brake fluids WO2004081155A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
BRPI0408234-6A BRPI0408234A (en) 2003-03-12 2004-03-11 brake fluid and use of it
EP04719421A EP1603996A1 (en) 2003-03-12 2004-03-11 Dot 4 brake fluids
MXPA05009288A MXPA05009288A (en) 2003-03-12 2004-03-11 Dot 4 brake fluids.
AU2004219905A AU2004219905A1 (en) 2003-03-12 2004-03-11 DOT 4 brake fluids
CA002517683A CA2517683A1 (en) 2003-03-12 2004-03-11 Dot 4 brake fluids
US10/548,173 US20060264337A1 (en) 2003-03-12 2004-03-11 Dot 4 brake fluids
JP2006500058A JP2006519887A (en) 2003-03-12 2004-03-11 DOT4 brake fluid
NO20054265A NO20054265L (en) 2003-03-12 2005-09-15 DOT 4 Brake Bags

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2003110757 DE10310757A1 (en) 2003-03-12 2003-03-12 Brake fluid, used in motor vehicles, especially in regions with high humidity, comprises diethylene glycol and/or dipropylene glycol and (poly)ethylene glycol and/or (poly)propylene glycol monoalkyl ether
DE10310757.6 2003-03-12

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CN101955840A (en) * 2010-08-24 2011-01-26 柳盛春 High boiling point boric acid ester type synthetic brake fluid and preparation method thereof
CN103710115A (en) * 2013-12-27 2014-04-09 杨毅 Antilock material for engine crankshaft

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CA2517683A1 (en) 2004-09-23
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KR20050107607A (en) 2005-11-14
ZA200507266B (en) 2007-04-25
JP2006519887A (en) 2006-08-31
TW200502379A (en) 2005-01-16
CN1759165A (en) 2006-04-12
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BRPI0408234A (en) 2006-03-01
US20060264337A1 (en) 2006-11-23

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