EP0011730B2 - Fluides de freinage à action conservatrice ayant une teneur en acide oléique - Google Patents
Fluides de freinage à action conservatrice ayant une teneur en acide oléique Download PDFInfo
- Publication number
- EP0011730B2 EP0011730B2 EP79104326A EP79104326A EP0011730B2 EP 0011730 B2 EP0011730 B2 EP 0011730B2 EP 79104326 A EP79104326 A EP 79104326A EP 79104326 A EP79104326 A EP 79104326A EP 0011730 B2 EP0011730 B2 EP 0011730B2
- Authority
- EP
- European Patent Office
- Prior art keywords
- brake
- weight
- formula
- oleic acid
- brake fluids
- 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.)
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- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/20—Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
- C10M107/30—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M107/32—Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
- C10M107/34—Polyoxyalkylenes
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- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/78—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing boron
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- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/28—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/38—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
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- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
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- 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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- 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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- C10M2207/128—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 containing hydroxy groups; Ethers thereof
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Definitions
- Brake fluids with a preservative effect containing oleic acid Brake fluids with a preservative effect containing oleic acid.
- the invention relates to brake fluids based on polyglycol ethers and polyglycols containing fatty acids.
- DOT-3 brake fluids generally have good corrosion protection against tinplate, steel, cast iron, brass, copper and aluminum. Corrosion protection is only guaranteed if the metals are completely immersed in the liquid or otherwise well wetted by it.
- a major disadvantage of this brake pastes is that they greatly increase in re-filling of the brake system with brake fluid, the viscosity, so that the viscosity of the filled fluid under circumstances, the maximum viscosities of 1,500.10- 3 m 2 / s at -40 ° C substantially exceeds. Such mixtures then no longer meet the requirements of FMVSS 116, DOT3.
- Brake fluids containing corrosion-inhibiting oleic acid based on polyglycol ethers and polyglycols are already known from British patent specification 1,081,294.
- di- or trialkylene glycols should be used according to the teaching of the patent mentioned.
- these brake fluids provide insufficient rust protection in moisture corrosion tests compared to the brake fluids of the invention.
- a brake fluid consisting of a) 20% by weight polypropylene glycol with an average molecular weight of 2000; b) an alkenyl dicarboxylic acid anhydride; c) 78.2% by weight of a commercial, technical polyglycol ether mixture and d) antioxidants were available to the public prior to the priority date of the present patent.
- the task was therefore to propose brake fluids that can be used for impregnation at the same time and that allow the components to be stored for longer periods without corrosion.
- the high molecular weight polyalkylene glycols are carrier substances that have low water solubility and are characterized by high lipophilicity. This allows them to dissolve the oleic acid more, so that the concentration of oleic acid in the brake fluid can be up to 3%.
- Polyalkylene glycols of the formula I contained therein can consist solely of polypropylene glycols or can be prepared by mixing predominantly polypropylene glycols with polyethylene glycols or by reacting mixtures of ethylene oxide and (in excess) propylene oxide, statistical mixtures of compounds being formed which on average contain more propylene oxide than ethylene oxide residues and have molecular weights in the specified range.
- polyethylene glycols can also be reacted with propylene oxide or polypropylene glycols with ethylene oxide, the starting polyglycols the amount of alkylene oxides and the polymerization conditions being chosen so that polyalkylene glycols according to the formula with the molecular weights specified there of 500 to 3000, preferably 1800 to 2200, are formed.
- the procedure is expediently such that an epoxy mixture consisting of the desired molar ratios of ethylene oxide and propylene oxide is polymerized by methods known per se.
- Oleic acid is used as corrosion inhibitor.
- the basic components are the polyglycol ethers of the formula 11 which are customary in brake fluids, for example
- the brake fluids according to the invention can also contain boric acid esters of glycol ethers of the formula 11, e.g. in amounts of 20 to 50% by weight.
- Suitable boric acid esters are e.g. Methyl-tri-glycol-ortho-bora, ethyl-tri-glycol-ortho-borate, methyl / ethyl-di / tri-ortho-borate.
- cast iron wheel brake cylinders are halved on the long side, cleaned with isopropanol and dried well.
- the halved brake cylinder is then immersed in the brake fluid for 5 seconds each, drained for 5 seconds and stored in a closed container over a water vapor-saturated atmosphere.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Lubricants (AREA)
Claims (1)
- Liquides de frein à base d'éthers de polyglycols et de polyglycols ayant une teneur en acides gras, caractérisés en ce qu'ils contiennentA) 10 à 40% en poids, sur la base du liquide de frein, de polyalkylèneglycols, sous forme de composés unique ou de mélanges, de formule 1B) 0,1 à 3% en poids d'acide oléique, et, pour compléter à 100%, les composants suivants:C) des éthers de polyglycols de formuleD) le cas échéant, des polyglycols de l'oxyde d'éthylène et/ou de l'oxyde de propylène ayant un poids moléculaire dans la gamme des poids moléculaires des lubrifiants utilisés d'habitude dans des liquides de frein, et/ouE) le cas échéant, 20 à 50% en poids d'esters de l'acide borique et d'éthers de glycol de formule Il etF) de petites quantités d'antioxydants et d'inhibiteurs connus en soi, choisis dans le groupe composé par le benzotriazole, l'imidazole, l'imidazoline, des amines primaires, secondaires, des éthanolamines, le bisphénol A, le triphénylphos- phite ou le 2,4-di-tert.butylcrésol.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2851057 | 1978-11-25 | ||
DE19782851057 DE2851057A1 (de) | 1978-11-25 | 1978-11-25 | Bremsfluessigkeiten mit konservierender wirkung |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0011730A1 EP0011730A1 (fr) | 1980-06-11 |
EP0011730B1 EP0011730B1 (fr) | 1982-10-06 |
EP0011730B2 true EP0011730B2 (fr) | 1986-06-04 |
Family
ID=6055539
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP79104326A Expired EP0011730B2 (fr) | 1978-11-25 | 1979-11-06 | Fluides de freinage à action conservatrice ayant une teneur en acide oléique |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0011730B2 (fr) |
DE (2) | DE2851057A1 (fr) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1227061B (it) * | 1988-09-13 | 1991-03-14 | Lubritalia Spa | Fluidi idrodinamici di sicurezza resistenti alla propagazione della fiamma e con elevata temperatura di autoaccensione e procedimento per la loro preparazione. |
US6855676B2 (en) | 2002-02-11 | 2005-02-15 | Ecolab., Inc. | Lubricant for conveyor system |
BRPI0916028A2 (pt) * | 2008-11-07 | 2015-11-10 | Dow Global Technologies Inc | composição de fluido |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2434978A (en) * | 1944-04-15 | 1948-01-27 | William A Zisman | Anticorrosion additives for synthetic lubricants |
NL302392A (fr) * | 1962-12-28 | |||
GB1388012A (en) * | 1972-02-09 | 1975-03-19 | Shell Int Research | Hydraulic fluids and their preparation |
-
1978
- 1978-11-25 DE DE19782851057 patent/DE2851057A1/de not_active Withdrawn
-
1979
- 1979-11-06 EP EP79104326A patent/EP0011730B2/fr not_active Expired
- 1979-11-06 DE DE7979104326T patent/DE2963824D1/de not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE2963824D1 (en) | 1982-11-11 |
EP0011730A1 (fr) | 1980-06-11 |
DE2851057A1 (de) | 1980-06-12 |
EP0011730B1 (fr) | 1982-10-06 |
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