JP5480285B2 - Low viscosity functional fluid - Google Patents

Description

TECHNICAL FIELD This application claims the benefit of the filing date of US Application Serial No. 61 / 112,466 (filed November 7, 2008), which is incorporated herein by reference in its entirety.

  The present disclosure relates to low viscosity functional fluids useful for various applications and particularly as brake fluids.

Background Newly developed equipment, such as electronic or automatic anti-lock braking systems, stability control systems, and regenerative braking systems, is a high performance hydraulic fluid (e.g., brake fluid) with appropriate physical and performance characteristics. Has created a demand for. In particular, there is a strong need for high performance brake fluids that have high lubricity to reduce or eliminate brake noise while improving corrosion life by reducing corrosion. The US government has developed a standard governing the designation and warranty of functional fluids used as brake fluids using DOT (Department of Transportation) designation systems (eg DOT 3, DOT 4, DOT 5.1, etc.). It was. The standard is implemented by the Federal Motor Vehicle Safety Standard 116 (“FMVSS 116”). In addition, certain standards setting agencies, such as Society of Automotive Engineers (“SAE”) and International Standards Organization (“ISO”), have developed their own standards and guarantees for brake fluids. SAE Standard J1703 covers non-petroleum brake fluids with specific physical properties including those shown below. SAE standard J1704 covers "borate ester brake fluids" that achieve the above level of performance of the SAE J1703 standard. Similarly, ISO 4925 provides a number of brake fluid designations for use outside the United States, such as “Class 3,” “Class 4,” “Class 5-1,” and “Class 6.”

  FMVSS 116, SAE J1703, SAE J1704, and ISO 4925 have strict physical properties and performance requirements, especially minimum dry equilibrium reflux boiling point (ERBP), minimum wet equilibrium boiling point (WERBP), and maximum low temperature (−40 ° C.) viscosity. Give against. They also require maintaining appropriate corrosion resistance, stability and other specific physical properties such as pH, storage alkalinity, rubber swelling and the like. SAE J1703 (Rev. April 2004) and J1704 (Rev. April 2004) and FMVSS 116 are all incorporated herein by reference.

  The recent standards for brake fluid are listed below.

  One exemplary solution for providing such desirable functional fluids was introduced in co-owned US Patent Application Publication No. 2007/0027039 (Title of Invention “Low Viscosity Functional Fluids”). And incorporated herein by reference for all purposes. Advantageously, it has been found that the desirable properties of these prior art functional fluids can be further improved, especially in the areas of lubricity and corrosion resistance. Furthermore, it has been discovered that such improvements can be realized without incurring significant costs. In addition, it may be possible to actually reduce costs through the use of new ingredients, as well as prior art ingredients or other alternative ingredients of such functional fluids.

  Many newer brake system master cylinders include a plastic lining that is engaged by a rubber cup on the master cylinder piston when the brake is activated. Many known brake fluids have been found to provide insufficient lubricity in such applications, resulting in excessive noise and wear. It may be possible to reduce such noise and wear through the use of modified functional fluids.

  FMVSS 116, J1703, J1704, and ISO 4925 each have specified test procedures (where various metal strips of metal in a mixture of 5% (by volume) water and brake fluid for a specific time ( 120 hours), including corrosion specifications based on a specific temperature (100 ° C.). The standards of FMVSS 116, J1703, J1704, and ISO 4925 are based on actual road conditions (which provide a lot of brake fluid), especially in the northern climate of the United States (often in winter, salinity to control ice accumulation). It was found that the road surface in (provided) does not reproduce with high reliability. As a result, it has been proposed to modify the test procedure used to assess corrosion by adding a chloride salt (eg, NaCl) to the water / brake fluid mixture. However, current brake fluids cannot provide the level of corrosion resistance required for DOT 3, DOT 4, J1703, J1704 and ISO 4925 fluids when subjected to this modified test. For example, Shannon, US Pat. No. 6,558,569, and Park, US Pat. No. 6,339,050 describe a DOT 4 brake fluid comprising an alkyl glycol borate ester, an alkyl glycol, and a corrosion inhibitor package. . However, they do not address the problem of brake fluid contamination with salt water and provide an indication that the disclosed fluid can meet SAE J1703 / J1704 or ISO 4925 corrosion standards when subjected to a salt water environment. Absent. Thus, there is a need for functional fluids that address the above problems.

SUMMARY A fluid composition comprising an additive package comprising at least one glycol and at least one fatty acid and at least one phosphate ester is provided. In certain exemplary embodiments, the at least one fatty acid is an aliphatic carboxylic acid having at least 2, preferably at least 5, more preferably at least 10, and even more preferably at least 15 carbon atoms. . In another exemplary embodiment, the at least one fatty acid has no more than 35, preferably no more than 30, and even more preferably no more than 25 carbon atoms. In further exemplary embodiments, the fatty acid is monounsaturated. The fatty acid in the additive package is generally in an amount that is at least about 0.01%, preferably at least about 0.04%, and more preferably at least about 0.08% by weight of the fluid composition. Exists. The fatty acid is generally present in an amount that is no greater than 0.4%, more preferably no greater than about 0.2%, and even more preferably no greater than about 0.15% by weight of the fluid composition.

The phosphate ester is generally a mono-, di- or tri-ester of alcohol and phosphoric acid (H ₃ PO ₄ ). The alcohol preferably has the formula R ₁ —R ₂ —OH, wherein R ₁ is a substituted or unsubstituted alkyl group, alkenyl group or aryl group, and more preferably at least three. Even more preferably having at least 4 and even more preferably at least 6 carbon atoms. R ₁ has no more than 30, preferably no more than 28, even more preferably no more than 26, and even more preferably no more than 24 carbon atoms. R ₂ is preferably an alkyl group or an alkoxy group and has 2 to 6 carbon atoms. In one exemplary embodiment, R ₂ is an ethoxy group (—O—CH ₂ —CH ₂ —).

  When the fluid is applied between a first surface comprising a glass fiber / polyamide 66 composite and a second surface comprising 80 Shore A hardness EPDM rubber, comprising at least one glycol and additive package. A fluid composition is also provided wherein the coefficient of friction after 100 seconds of sliding engagement between the first surface and the second surface is less than about 0.07. In certain exemplary aspects, the coefficient of friction after 100 seconds of sliding engagement is less than about 0.03. In another exemplary embodiment, the fluid has an equilibrium reflux boiling point of at least about 230 ° C. In another exemplary embodiment, the fluid has a kinematic viscosity of about 1800 cSt or less at −40 ° C. In certain exemplary applications, the fluid is used as a master cylinder lubricant.

FIG. 1 is a plot of friction data for a first low viscosity glycol-based fluid and two modified fluids containing oleic acid and / or phosphate esters. FIG. 2 is a plot of friction data for two modified versions of a second low viscosity glycol based fluid and a fluid containing various amounts of phosphate ester.

DETAILED DESCRIPTION The present disclosure relates to a functional fluid that includes an additive package that includes one or more glycols and at least one fatty acid and a phosphate ester. Fatty acids and phosphate esters are preferably present in an amount effective to assist lubrication of the frictionally engaged surfaces to prevent corrosion when the fluid is contaminated with brine.

  The functional fluids described herein generally have a total glycol of greater than about 20% by weight, more preferably greater than about 40% by weight total glycol, and even more preferably greater than about 60% by weight total glycol. including. It is even more preferred that the total glycol amount be greater than about 70% by weight, and it is especially preferred that the total glycol amount be greater than about 80% by weight. The total amount of glycol is preferably less than 100% by weight of the total functional fluid composition and preferably no more than about 99% by weight of the total fluid composition.

  The glycol component can be formed of one, two, three or more glycols, polyglycols, or some, substantially all (at least 90% or at least 95%) or all of both. Preferably, the glycol or polyglycol of the glycol component is of the formula I:

Have

Each of R ₁ , R ₂ , R ₃ , R ₄ , R ₅ is either hydrogen (H), or an alkyl group containing 1-8 or more carbon atoms, or a mixture thereof; For example, provisional application serial number 60 / 976,010 (filed on Sep. 28, 2007), the title of the invention "Functional Fluid Composition" (incorporated herein by reference in its entirety). R ₁ is preferably an alkyl group containing 1 to 8 carbon atoms, such as an alkyl end-capped glycol ether, where the glycol or polyglycol is an alkoxy glycol ether (a glycol in which R ₁ is simply H). Conversely). Typically, R ₁ is less than 90%, more typically less than 50%, and even less than 30% or less than 20% by weight of the glycol component, the entire fluid composition, or both. , H. The term “polyglycol” means a glycol, eg, one of formula I where n is at least 2 or greater. The term “glycol” encompasses all polyglycols. It should be understood that the glycol component can include both glycols where R ₁ is an alkyl group and those where R ₁ is H.

  The glycol component can include a glycol where n = 1. When included, such glycols are less than about 5% by weight of the glycol component. Preferably, the glycol of the glycol component is glycol (eg, alkoxy glycol) where n = 2, glycol (eg, alkoxy glycol) where n = 3, glycol (eg, alkoxy glycol) n = 4 or more, or any mixture thereof. More preferred glycol components include a mixture of glycols (eg, alkoxy glycols), where n = 2, n = 3, and n = 4 or more. n = 2 or more glycols in the glycol component and / or in the entire functional fluid, at least about 50%, more preferably at least about 60%, and more preferably in the glycol component, the entire functional fluid or both Is preferably present in an amount that is at least about 75% by weight. The amount of glycol in which n is 2 or more is even more preferably at least about 90% by weight.

  It is also preferred that n = 2 or more glycols are present in the glycol component and / or the entire functional fluid in an amount of about 99% by weight or less.

  The glycol with n = 2 is preferably at least about 0.5% by weight of the total glycol component, more preferably at least about 1% by weight of the total glycol component, and even more preferably at least about 2% by weight of the total glycol component. Present in quantity. The amount of glycol where n = 2 is preferably no more than about 10% by weight of the total glycol component, more preferably no more than about 8% by weight of the total glycol component, and even more preferably no more than about 7% by weight of the total glycol component. Exists.

  The glycol where n = 3 is preferably an amount that is preferably no greater than about 80% by weight of the total glycol component, more preferably no greater than about 70% by weight of the total glycol component, and even more preferably no greater than about 66% by weight of the total glycol component. Exists. The glycol with n = 3 is preferably present in an amount that is at least about 40% by weight of the total glycol component, more preferably at least about 50% by weight, and even more preferably at least about 58% by weight of the total glycol component.

N = 4 or more glycols are present in an amount that is preferably no greater than about 45%, more preferably no greater than about 40%, and even more preferably no greater than about 35% by weight of the total glycol component. N = 4 or more glycols are present in an amount that is preferably at least about 15%, more preferably at least about 20%, and even more preferably at least about 25% by weight of the total glycol component. Preferred glycol components include those in which the R ₁ group includes methyl, ethyl, propyl, butyl, or combinations thereof.

Non-limiting examples of useful glycols (eg, alkoxy glycols or others) include methoxytriglycol, methoxydiglycol, methoxytetraglycol, methoxypolyglycol (eg, methoxytriglycol, methoxytetraglycol, and other glycols) R ₁ is CH ₃ and n is 5 or larger), ethoxytriglycol, ethoxydiglycol, ethoxytetraglycol, propoxytriglycol, butoxytriglycol (eg, triethylene glycol monobutyl ether) , Butoxydiglycol (eg, diethylene glycol monobutyl ether), butoxytetraglycol, butoxypolyglycol (eg, butoxytriglycol, butoxyte) And other glycols wherein R ₁ is alkyl having 4 carbon atoms and n is 5 or larger), butoxypentoxydiglycol, pentoxytriglycol, 2-ethylhexyl Diglycols, as well as any mixtures thereof, can be mentioned.

  Preferred glycols for the glycol component (eg, alkoxy glycol) include, but are not limited to, methoxytriglycol, methoxydiglycol, methoxypolyglycol, methoxytetraglycol, ethoxypolyglycol, ethoxytriglycol, ethoxydiglycol, ethoxytetraglycol, butoxy Polyglycol, butoxytriglycol, butoxydiglycol, butoxytetraglycol, triethylene glycol monohexyl ether, diethylene glycol monopropyl ether, triethylene glycol monopropyl ether, dipropylene glycol monomethyl ether, dipropylene glycol monopropyl ether, tripropylene glycol Monopropyl ether, dipropylene glycol monob Ether, tripropylene glycol monobutyl ether, polypropylene glycol monobutyl ether, polypropylene glycol monopropyl ether, or mixtures thereof. More preferred alkoxy glycol components are methoxy triglycol, methoxy diglycol, methoxy polyglycol, butoxy triglycol, butoxy diglycol, butoxy polyglycol, triethylene glycol monohexyl ether, diethylene glycol monopropyl ether, triethylene glycol monopropyl ether, Dipropylene glycol monomethyl ether, dipropylene glycol monopropyl ether, tripropylene glycol monopropyl ether, dipropylene glycol monobutyl ether, tripropylene glycol monobutyl ether, polypropylene glycol monopropyl ether, polypropylene glycol monobutyl ether, or mixtures thereof. The most preferred alkoxy glycol component is methoxy polyglycol, butoxy diglycol, butoxy triglycol, butoxy polyglycol, triethylene glycol monopropyl ether, tripropylene glycol monopropyl ether, tripropylene glycol monobutyl ether, polypropylene glycol monopropyl ether, or Contains a mixture of two or more of polypropylene glycol monobutyl ether.

  Further examples of useful glycols such as, but not limited to, diethylene glycol monopropyl ether, triethylene glycol monopropyl ether, dipropylene glycol monomethyl ether, dipropylene glycol monopropyl ether, tripropylene glycol monopropyl Ether, dipropylene glycol monobutyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monoethyl ether, tripropylene glycol monopropyl ether, tripropylene glycol monobutyl ether, polypropylene glycol monopropyl ether, polypropylene glycol monobutyl ether, polybutylene glycol monopropyl Ether, polybutylene Glycol monomethyl ether, combinations thereof and the like.

  Without limitation, a useful method for preparing alkoxy glycols includes an alkoxylation reaction in which an alkylene oxide is reacted with an alcohol to produce an alkoxy glycol.

The glycol component can also include glycol polymers, which can be homopolymers, block copolymers, random copolymers, and the like. Glycol copolymers are preferred. The glycol copolymer typically comprises one or more first repeat units of formula I having a first structure and one or more second repeat units having a second structure. In particular, the glycol copolymer typically comprises at least one first repeat unit of formula I, wherein R ₂ , R ₃ , R ₄ and R ₅ are each H. Glycol copolymers are also typically at least one and typically only one of R ₂ , R ₃ , R ₄ and R ₅ , but in some cases two, three or all four are Each includes at least one second repeat unit, which is an alkyl group containing 1 to 8 carbon atoms. Preferred second repeat units of the glycol copolymer include those in which the R ₂ or R ₃ group, and more preferably the R ₄ or R ₅ group, includes methyl, ethyl, propyl, butyl, or combinations thereof. It is done. More preferred second repeat units of the glycol copolymer include those in which the R ₂ or R ₃ group, and more preferably the R ₄ or R ₅ group contains a methyl or ethyl group. Even more preferred second repeat units of the glycol copolymer include those wherein the R ₂ or R ₃ group, and more preferably the R ₄ or R ₅ group, contains a methyl group (ie, a propylene oxide repeat unit). It is done.

In one exemplary embodiment, the glycol polymer has the formula:
_{R 7 - (O- (PO)} m (EO) n -R 8) x
(Wherein PO is a propylene oxide unit;
EO is an ethylene oxide unit;
R ₈ is hydrogen or a hydrocarbyl group;
x is at least 1;
R ₇ is hydrogen or an x-valent hydrocarbyl group;
m is a number of at least 0;
n is a number of at least 0; and m + n is greater than 0. )
Have

  The glycol polymer has a molecular weight of at least about 500 g / mol, preferably at least about 750 g / mol, and more preferably at least about 900 g / mol. The glycol polymer has a molecular weight of about 2,000 g / mol or less, more preferably about 1,500 g / mol or less, and even more preferably about 11,110 g / mol or less.

According to one exemplary embodiment of a glycol copolymer, m and n are equal, in which case the glycol copolymer contains equimolar ethylene oxide and propylene oxide repeating units. The number of repeating ethylene oxide units and the number of propylene oxide units are each preferably more than 2, more preferably more than 4, and even more preferably more than 8. One suitable glycol copolymer is UCON® 50HB-260 (The Dow Chemical Company). UCON 50 HB-260 contains an equal number of propylene oxide units and ethylene oxide units and has a molecular weight of about 1,000 g / mol. In UCON 50 HB-260, R ₇ is a monovalent alkyl group, x is 1 and R ₈ is a hydrogen atom.

  When used, the glycol borate ester component preferably has the formula:

Wherein R ₁ , R ₂ , R ₃ , R ₄ and R ₅ can be any group as defined for formula I, and n can be as defined for formula I. )
The at least 1 type of containing component which has is mentioned. Thus, the glycol borate ester component can have any repeat unit of the glycol component as discussed herein with respect to Formula I. It is also understood that the glycol borate ester component and any borate-containing compound are not considered part of the glycol component but are considered separate.

  Examples of optional glycol borate ester components include alkoxy glycol borate ester components such as methoxytriethylene glycol borate ester, ethoxytriethylene glycol borate ester, butoxy triethylene glycol borate ester and mixtures thereof, which are disclosed in US Pat. No. 558,569 (incorporated herein by reference). When the borate ester component is present in the composition, it is preferably present in an amount that is greater than about 1% by weight of the functional fluid. The optional borate ester is also preferably present in an amount that is less than about 10% by weight and more preferably less than about 4% by weight of the functional fluid. In one embodiment, the functional fluid composition is substantially free (less than about 0.5% by weight of the functional fluid) or completely free of any borate ester component.

  When a glycol borate ester component is included in the composition, this is typically the case when the glycol group of the component represents a substantial portion of the entire composition. Glycol groups as defined herein are part of Formula I and Formula II and are attached to the (H) hydrogen atom or (B) boron atom of these formulas. Thus, such glycol groups are as follows:

  These glycol groups represent at least about 50%, more preferably at least about 60%, even more typically at least about 80%, and even in some cases at least about 90% by weight of the total composition. be able to.

  As noted above, the functional fluid of the present disclosure also includes at least one fatty acid, at least one phosphate ester, one or more corrosion inhibitors, and the following: antifoaming agents, pH stabilizers, chelating agents, and antioxidants. Including an additive package containing one or more agents. Corrosion inhibitors in the additive package preferably include compounds that prevent corrosion of tinned iron, steel, aluminum, cast iron, brass and copper, each of which is listed in SAE J1703, SAE J1704 and FMVSS 116. Has the stated corrosion specifications. However, in a particularly preferred embodiment, the corrosion inhibitor also includes one or more compounds that prevent zinc corrosion.

  The additive package is preferably at least about 0.1% by weight of the fluid composition, more preferably at least about 0.2% by weight of the fluid composition, and most preferably at least about 0.3% by weight of the fluid composition. Is present in an amount. The additive package is preferably no more than about 10% by weight of the fluid composition, more preferably no more than about 6.0% by weight of the fluid composition, and most preferably no more than about 4.0% by weight of the fluid composition. Present in quantity.

  The fatty acid in the additive package is preferably one or more aliphatic carboxylic acids having at least 2, preferably at least 5, more preferably at least 10, and even more preferably at least 15 carbon atoms. Examples include acids. Aliphatic carboxylic acids generally have no more than 35, preferably no more than 30, and more preferably no more than 25 carbon atoms. Linear, monofunctional fatty acids are preferred, and linear, unsaturated, monofunctional fatty acids are more preferred. Monounsaturated fatty acids are particularly preferred. Suitable fatty acids include, but are not limited to, oleic acid, palmitic acid, stearic acid, myristic acid, palmitoic acid, elaidic acid, and linoleic acid. The fatty acid in the additive package is generally in an amount that is at least about 0.01%, preferably at least about 0.04%, and more preferably at least about 0.08% by weight of the fluid composition. Exists. The fatty acid is generally present in an amount that is no more than about 0.4%, more preferably no more than about 0.2%, and most preferably no more than about 0.15% by weight of the fluid composition.

The one or more additives in the additive package are generally phosphates, and more specifically phosphate esters. The phosphate ester is generally a mono-, di-, or tri-ester of alcohol and phosphoric acid (H ₃ PO ₄ ). The alcohol is preferably of the formula:
Formula III R ₁ —R ₂ —OH
Wherein R ₁ is a substituted or unsubstituted alkyl having at least 2, more preferably at least 3, even more preferably at least 4, and even more preferably at least 6 carbon atoms. Group, alkenyl group or aryl group. R ₁ preferably has no more than 30, more preferably no more than 28, even more preferably no more than 26, and even more preferably no more than 24 carbon atoms. R ₂ is preferably an alkyl or alkoxy group having 2 to 6 carbon atoms. In one exemplary embodiment, R ₂ is an ethoxy group (—O—CH ₂ —CH ₂ —). Suitable phosphate esters include, but are not limited to, RHODOFAC® RM-510 (Rhodia), dinonylphenol, ethoxylation, phosphate ester, LUBRHOPHOS® LP-700 (Rhodia), phosphate ester of ethoxylated phenol. , LUBRHOPHOS® LB-400 (Rhodia), ethoxylated phosphate ester of olein alcohol, LUBRHOPHOS® LK-500 (Rhodia), phosphate ester of ethoxylated hexanol, and tricresyl phosphate, phosphate tris of cresol Examples include esters.

  The phosphate ester is preferably present in an amount that is at least about 0.05%, more preferably at least about 0.1%, and even more preferably at least about 0.15% by weight of the functional fluid. The phosphate ester is preferably present in an amount that is no greater than about 0.4%, more preferably no greater than about 0.3%, and even more preferably no greater than about 0.25% by weight of the functional fluid. While not wishing to be bound by any theory, as further described below, the combination of a phosphate ester and a fatty acid in the functional fluid additive package unexpectedly improves the lubricity of the functional fluid. This is considered to give a synergistic effect.

  The corrosion inhibitor preferably includes at least one heterocyclic nitrogen-containing compound, such as triazoles such as benzotriazole, tritriazole, 1,2,4-triazole, and mixtures thereof. The triazole compound is present in an amount that is preferably at least about 0.01%, more preferably at least about 0.05%, and most preferably at least about 0.09% by weight of the total fluid weight. The triazole compound is preferably present in an amount that is no greater than about 0.4%, more preferably no greater than about 0.3%, and most preferably no greater than about 0.20% by weight of the total fluid composition. Without wishing to be bound by any theory, triazole compounds such as benzotriazole, tritriazole, and 1,2,4-triazoal are believed to be particularly effective in preventing copper corrosion.

  The corrosion inhibitor also preferably includes amine compounds other than triazoles, such as alkylamines (eg, di-n-butylamine and di-n-amylamine), cyclohexylamine, piperazine (eg, hydroxyethylpiperazine), and these Of the salt. Nontriazoleamine compounds that are particularly useful as corrosion inhibitors in the functional fluid compositions of the present disclosure include alkanolamines, preferably containing 1 to 3 alkanol groups, each alkanol group containing 1 to 6 carbon atoms. To do. Examples of useful alkanolamines include mono-, di- and trimethanolamine, mono-, di- and triethanolamine, mono-, di- and tripropanolamine, and mono-, di- and triisopropanolamine. Can be mentioned. Preferred alkanolamines include butyl diethanolamine and diisopropanolamine (“dipa”). Without wishing to be bound by any theory, it is believed that alkanolamines are useful for preventing corrosion of ferrous compounds (eg, iron, steel) and also act as buffers. .

  The non-triazole amine compound is preferably present in an amount that is at least about 0.1%, more preferably at least about 0.5%, and even more preferably at least about 0.8% by weight of the total fluid composition. . The non-triazole amine compound is present in an amount that is preferably no greater than about 3%, more preferably no greater than about 2.0%, and most preferably no greater than about 1.5% by weight of the total fluid composition.

  The corrosion inhibitor can include one or more alkenyl succinic anhydrides. Preferred alkenyl succinic anhydrides include maleic anhydride derivatives. Dodecenyl succinic anhydride is particularly preferred. When included in the functional fluid, the alkenyl succinic anhydride is preferably at least about 0.1%, more preferably at least about 0.12%, and most preferably at least about 0% of the functional fluid composition. Present in an amount which is 14% by weight. The alkenyl succinic anhydride is present in an amount that is preferably no greater than about 0.5%, more preferably no greater than about 0.3%, and most preferably no greater than about 0.2% by weight of the functional fluid composition. .

  In certain preferred embodiments, the corrosion inhibitor also includes one or more inorganic nitrates, preferably sodium nitrate. The inorganic nitrate is preferably present in an amount that is at least about 0.01%, more preferably at least about 0.015%, and most preferably at least about 0.02% by weight of the fluid composition. The inorganic nitrate is present in an amount that is preferably no greater than about 0.06%, more preferably no greater than about 0.05%, and most preferably no greater than about 0.04% by weight of the fluid composition. While not wishing to be bound by any theory, it is believed that inorganic nitrates are effective in preventing aluminum corrosion.

Corrosion inhibitors include one or more inorganic borates, such as sodium tetraborate (commonly known as Borax). Inorganic borates are preferably provided as solid hydrates. A particularly preferred inorganic borate is sodium tetraborate pentahydrate Na ₂ B ₄ O ₇ .5H ₂ O (also known as Borax 5 Mol). Another exemplary inorganic borate is sodium tetraborate decahydrate (Na ₂ B ₄ O ₇ .10H ₂ O). When present, the inorganic borate is provided in an amount that is preferably at least about 0.03%, more preferably at least about 0.05%, and most preferably at least about 0.07% by weight of the fluid composition. . The inorganic borate is preferably provided in an amount that is no greater than about 0.1%, more preferably no greater than about 0.09%, and most preferably no greater than about 0.08% by weight of the fluid composition. Without wishing to be bound by any theory, it is believed that inorganic borates are effective in preventing corrosion of ferrous iron (eg, iron and steel).

  The corrosion inhibitor can also optionally include one or more silicone compounds, such as silicate esters. Preferred silicate esters include polymers of dialkoxysiloxanes, including but not limited to poly (diethoxysiloxane) (eg, PSI-021). The silicone corrosion inhibitor is preferably provided in an amount that is at least about 0.001%, more preferably at least about 0.003%, and most preferably at least about 0.004% by weight of the fluid composition. The silicone corrosion inhibitor is preferably provided in an amount that is no greater than about 0.008%, more preferably no greater than about 0.007%, and most preferably no greater than about 0.006% by weight of the fluid composition. Without wishing to be bound by any theory, it is believed that silicone corrosion inhibitors prevent brass and aluminum corrosion.

  In addition to the corrosion inhibitors described above, the functional fluid additive package can also include other additive compounds such as antifoaming agents, pH stabilizers, chelating agents, antioxidants, and the like. Preferred antifoaming agents include poly (dimethylsiloxane) and silicone compounds, such as SAG 100 Antifoam (a product of GE Advanced Materials). When present, the antifoaming agent is provided in an amount that is preferably no greater than about 0.00020% and more preferably no greater than about 0.00015% by weight of the fluid composition. The antifoaming agent is preferably present in an amount that is at least about 0.00001% and more preferably at least about 0.00005% by weight of the fluid composition.

  Suitable antioxidants include phenolic compounds and quinoline compounds. Exemplary phenolic antioxidants include BHT (butylated hydroxytoluene); 2,6-di-tert-butyl-4-methylphenol (manufactured by Great Lakes Chemical Corporation, name Lowinox® 624) 2 , 6-di-tert-butyl-p-cresol), 2,6-di-tert-butyl-4-sec-butylphenol (manufacturer SI Group, with name Isox® 132), and bisphenol A. It is done. Exemplary quinoline antioxidants include Agateite® Resin D, a polymerized trimethyldihydroquinoline compound (manufacturer RT. Vanderbilt Company). When antioxidants are included in the additive package, they are preferably at least about 0.1%, more preferably at least about 0.2%, and most preferably at least about 0.25% of the fluid composition. It is given in an amount that is mass%. The antioxidant is preferably provided in an amount that is no greater than about 1.0%, more preferably no greater than about 0.8%, and most preferably no greater than about 0.4% by weight of the fluid composition.

  Suitable chelating agents include trioctyl phosphine oxide, tributyl phosphate, dibutybutyl phosphate, DEHPA (di (2-ethylhexyl) phosphate) and propanediamine / xylene compositions such as Dupont Metal Deactivator (N, N'-disalicylidene -1,2-propanediamine and xylene). When used, the chelating agent is preferably present in an amount that is at least about 0.01 wt%, more preferably at least about 0.05 wt%, and most preferably at least about 0.08 wt%. The chelating agent is preferably present in an amount that is no greater than about 0.2%, most preferably no greater than about 0.15%, and most preferably no greater than about 0.13% by weight of the fluid composition.

As noted above, SAE J1703 and J1704 describe the corrosion criteria for DOT 3 and DOT 4 brake fluids, respectively. For both standards, two sets of six defined metal corrosion test strips are polished, cleaned and weighed. Six metal strips containing each set are secured together at one end. Each strip is approximately 8 cm long, 1.3 cm wide, 0.6 mm thick or less, and has a surface area of 25 ± 5 cm ² . The prescribed metals are copper, brass, cast iron, aluminum, steel, and tinned iron. Two styrene butadiene rubber (“SBR”) cups are prepared as described in Section 7.6 of FMVSS 116 and Appendix C and D of SAE J1704 (Rev. April 2004) and their base diameters are measured. To do. In addition, the International Rubber Hardness Degree (“IRHD”) value of the cup is evaluated using the ASTM D1415 test method, which is incorporated herein by reference in its entirety. Two SBR cups and two metal strip combinations are placed in a bottle containing brake fluid and 5% (by volume) water, where each metal strip combination is in one of the respective cups. Put in. Cap the bottle and place in an oven at 100 ° C. for 120 hours. The strip is then removed and dried at 23 ° C. ± 2 ° C. for 1 hour. After drying, each strip is weighed to the nearest 0.1 mg and the change in mass is calculated for each strip. The area of the strip is then evaluated and the mass change per unit area of surface area (mg / cm ² units) is calculated. The cup diameter and IRHD value are then evaluated. In order to be certified as DOT 4 brake fluid according to FMVSS 116, the mass change per unit surface area must not exceed the following specifications (same as those of SAE J1703 and J1704):

  In addition, the SMV cup specification of FMVSS 116 requires an International Rubber Hardness Degrees with an inner cup diameter increase of 1.4 mm or less and a hardness reduction of 15 or less. The SAE J1704 specifications are identical except that they require an SBR cup volume increase of 16% or less (instead of defining an increase in diameter). In addition, SAE J1703 and J1704 have a pH greater than 7.0 when the functional fluid is mixed with an equal volume of 50% ethanol / 50% distilled water mixture (neutralized to pH 7.0). And 11.5 or less. The standard also requires that the sediment level be 0.1 vol% or less. Each criterion also includes a low temperature appearance requirement (requiring the absence of stratification, precipitation, or crystallization under defined test conditions).

  As mentioned above, a modification of the brake fluid / water composition used to implement the SAE J1703 and SAE J1704 test procedures to better simulate an environment with a lot of brake fluid is proposed. It has been. In particular, many regions use road salt to keep the road free from ice and snow in winter. As a result, the brake fluid is often contaminated with water / salt solutions, which can reduce the performance of the brake fluid. In one preferred embodiment, when the functional fluid of the present disclosure is subjected to a J1703 / J1704 corrosion test using a brake fluid and a mixture of 5% water (by volume) and 25 ppm chloride ion, the mixture is J1703 / J1704 and FMVSS. Meets 116 corrosion specifications for maximum allowable mass change per surface area for tinned iron, steel, aluminum, cast iron, brass and copper.

  In addition to these corrosion inhibiting properties, the fluid compositions of the present disclosure exhibit excellent water stability and can maintain high boiling points and low viscosities at relatively high water levels. In certain preferred embodiments, the fluid composition maintains a wet equilibrium reflux boiling point (WERBP) of about 140 ° C. or higher, preferably about 150 ° C. or higher, more preferably about 200 ° C. or higher, and even more preferably about 220 ° C. or higher. . In certain preferred embodiments, the fluid composition maintains a dry equilibrium reflux boiling point (ERBP) of about 200 ° C. or higher, preferably about 220 ° C. or higher, more preferably about 230 ° C. or higher, and even more preferably about 240 ° C. or higher. . The functional fluid preferably has a kinematic viscosity at −40 ° C. of about 1800 cSt or less, more preferably about 1400 cSt or less, and most preferably about 1000 cSt or less.

Example
Example 1-Functional fluid corrosion and lubrication performance with phosphate ester and with phosphate ester / oleic acid combination Lubricant and corrosion test data is commercially available DOT 3 brake fluid (PM6664) Obtained for the base fluid and two modified versions of the fluid containing RHODOFAC® RM 510 phosphate ester. In one of the modified fluids, the phosphate ester is combined with a fatty acid (oleic acid) and in the other type is free of fatty acid. The formulation is as follows:

  In Table 3, “methoxypolyglycol” (“MPG”) is methoxytriethylene glycol (10 wt% MPG) methoxytetraethylene glycol (78.4 wt% MPG), and methoxy polyglycol 5 or It means a mixture of those having more repeating ethylene glycol units (10.9% by weight of MPG). The blend of LV-RG1 and LV-RG2 has the following equilibrium reflux boiling point and viscosity:

  Each of the fluids is tested for corrosion protection using the SAE J1703 and J1704 test protocols. Both with and without the addition of 25 ppm chloride ions to the water mixed with the functional fluid. The results are as follows:

  The functional fluids in Table 3 are also tested for lubricity using a Cameron-Print Reciprocating Sliding Wear Tester. Here, the upper sample containing 80 Durometer EPDM rubber vibrates against the lower sample containing Du Pont ZYTEL® 70G43 nylon 66 resin reinforced with 43% by weight glass fiber. The results are given in FIG. This plots the coefficient of friction versus time. As FIG. 1 shows, both LV-RG1 and LV-RG2 fluids achieve better lubricity (ie, lower coefficient of friction) than the base PM6664 material after about 90 seconds. As indicated above, unlike PM6664, both LV-RG1 and LV-RG2 fluids contain phosphate esters. However, LV-RG2 also contains oleic acid. As FIG. 1 shows, the combination of oleic acid and phosphate ester gives more than a 2-fold improvement in lubricity and more consistent lubricity over the test period. As Table 4 shows, both LV-RG1 and LV-RG2 meet the ERBP specifications of both SAE J1703 (ERBP 230 ° C. or higher) and SAE J1704 (ERBP 205 ° C. or higher). They also meet both standards of −40 ° C. kinematic viscosity specification (1800 cSt or less) and SAE J1703 WERBP specification (140 ° C. or more). In addition, even with the addition of 25 ppm chloride ion, both LV-RG1 and LV-RG2 corrode the tinned iron, steel, aluminum, cast iron, brass, and copper of both SAE J1703 and J1704. It conforms to the specifications, and the hardness and rubber cup diameter specifications of both standards.

Example 2-Corrosion and Lubrication Performance of Functional Fluids with Various Amounts of Phosphate Esters and No Fatty Acids In this example, lubricity and corrosion data were obtained from commercially available DOT 3 brake fluid (DBF 310 GC ) And two modified fluids with various amounts of RHODOFAC® RM-510 (dialkylphenol ethoxylated phosphate ester) added. The formulation is given in Table 7:

  In Table 7, “butoxypolyethylene glycol (“ BPG ”)” is butoxytriethylene glycol (11.9 wt% BPG), butoxytetraethylene glycol (64.2 wt% BPG), and butoxypolyethylene glycol. Or a mixture of those having more repeating ethylene oxide units (21.9% by weight of BPG). “Diflash purification” includes diethylene glycol (22.8 wt% Diflash), triethylene glycol (58.3 wt% Diflash), tetraethylene glycol (16.4 wt% Diflash), and ethylene glycol 5 Or a mixture of those having more repeating ethylene oxide units (1.8% by weight Diflash). “Pusher purification” includes tetraethylene glycol (65.3 wt% Pusher), pentaethylene glycol (29.2 wt% Pusher), hexaethylene glycol (1.8 wt% Pusher), and ethylene glycol. Means a mixture of 7 or more repeating ethylene oxide units (2.3% by weight Pusher).

  The fluids in Table 7 are subjected to SAE J1703 / J1704 and FMVSS 116 corrosion tests (both with and without the addition of 25 ppm chloride ions to the water added to the functional fluid). The results are listed in Tables 8 and 9 below:

  As Tables 8 and 9 show, the formulation of both 0.1% RM-510 and 0.2% RM-510 is SAE J1703 / 1704 for tinned iron, steel, aluminum, cast iron, brass, and copper. Meets corrosion specifications and these rubber cup diameter and hardness specifications.

  The functional fluids in Table 7 are also tested for lubricity using the Cameron-Print device described above for Example 1. The surface used in the Cameron-Print device is that used in Example 1. The resulting lubricity data is represented in FIG. As the figure shows, the addition of 0.1% RM-510 gives greater lubricity from 10 seconds to about 230 seconds. However, after about 230 seconds, the 0.1% RM-510 formulation suffers from reduced lubricity. In contrast, a formulation with 0.2% RM-510 maintains a coefficient of friction of less than about 0.06 throughout the test period. Both formulations in Table 7 contain phosphate ester (RM-510), but none of these contain fatty acids. In contrast, the LV-RG2 formulation of Table 3 contains both fatty acids and phosphate esters. The comparison of FIGS. 1 and 2 shows that the combination of oleic acid and RM-510 gives a substantial increase in lubricity, even when the amount of RM-510 is kept constant, It is further shown that the phosphate ester combination achieves a synergistic effect and unexpected improvement in lubricity.

  The functional fluids of the present disclosure are well adapted for use as hydraulic fluids for many mechanical systems (eg, hydraulic lifts, cranes, forklifts, bulldozers, hydraulic jacks, brake systems, combinations thereof, etc.) . The high lubricity of these fluid compositions, as well as the ERBP, WERBP, and low temperature viscosities, make them brake systems in the means of transport (eg, fixed and rotary wing airplanes, trains, automobile class 1-8, etc.). Be well adapted to These brake systems include anti-lock brake systems (ABS), stability control systems, or combinations thereof.

  In one exemplary implementation, a brake system is provided that includes a depressible actuator, a master cylinder, a piston, and a rubber cup seal disposed on the piston. The functional fluid of the present disclosure is disposed in the bore of the master cylinder and is used to transmit pressure to a brake mechanism (eg, brake pads and rotor) to slow down or stop the vehicle. As the actuator is pressed, the piston moves along the inside of the master cylinder, transferring fluid from the cylinder bore. During this operation, the rubber cup frictionally engages the wall of the master cylinder. This in turn can cause the rubber cup to rub and cause leakage around the rubber cup and reduced braking performance. In certain exemplary applications, the master cylinder is along the plastic and the functional fluid lubricates the frictional engagement of the rubber cup and plastic master cylinder lining. As illustrated in FIGS. 1 and 2, the use of a functional fluid comprising at least one glycol and an additive package comprising at least one fatty acid and at least one phosphate ester is used between the rubber and the plastic surface. The amount of friction is beneficially reduced, thereby reducing the degree of rubbing experienced by the rubber cup.

  It will be further understood that the function or structure of multiple components or steps can be combined into a single component or step, or that the function or structure of one step or component can be divided into multiple steps or components. The present disclosure contemplates all of these combinations. Unless stated otherwise, the dimensions and arrangements of the various structures presented herein are not intended to be limiting and other dimensions or arrangements are possible. Multiple structural components or steps can be provided by a single integrated structure or step. Alternatively, a single integrated structure or step may be divided into separate components or steps. In addition, while features of the present disclosure may have been described in the context of only one example aspect, such feature may be one or more other features of other aspects for any given application. Can be combined with. From the foregoing, it will also be appreciated that the fabrication of unique structures herein and their operation also constitutes a method according to the present disclosure.

（式中、Ｒ ₁ 、Ｒ ₂ 、Ｒ ₃ 、Ｒ ₄ およびＲ ₅ は独立に、水素、および１〜８個の炭素原子を含有するアルキル基からなる群から選択され、そしてｎは少なくとも１である。）
を有する、上記［１］〜［３］のいずれかに記載の流体組成物。
［５］ 少なくとも１種のグリコールが、ｎ＝２である第１のグリコール成分と、ｎ＝３である第２のグリコール成分とを含む、上記［４］に記載の流体組成物。
［６］ 少なくとも１種のグリコール成分が、Ｒ ₁ が１個の炭素原子を含有するアルキル基である第１のグリコール成分と、Ｒ ₁ が４個の炭素原子を含有するアルキル基である第２のグリコール成分とを含む、上記［４］または［５］に記載の流体組成物。
［７］ 流体組成物の約７０質量％未満である量で存在する少なくとも１種のグリコールボレートエステルを更に含む、上記［１］〜［６］のいずれかに記載の流体組成物。
［８］ 添加剤パッケージが、流体組成物の約１０質量％未満である量で存在する、上記［１］〜［７］のいずれかに記載の流体組成物。
［９］ 添加剤パッケージが、流体組成物の約０．１質量％超である量で存在する、上記［１］〜［８］のいずれかに記載の流体組成物。
［１０］ 少なくとも１種の脂肪酸が、直鎖である、上記［１］〜［９］のいずれかに記載の流体組成物。
［１１］ 少なくとも１種の脂肪酸が、モノ不飽和である、上記［１］〜［１０］のいずれかに記載の流体組成物。
［１２］ 少なくとも１種の脂肪酸が、流体組成物の少なくとも約０．０１質量％の量で存在する、上記［１］〜［１１］のいずれかに記載の流体組成物。
［１３］ 脂肪酸が、流体組成物の約０．４％以下の量で存在する、上記［１］〜［１２］のいずれかに記載の流体組成物。
［１４］ ホスフェートエステルが、式Ｒ ₁ −Ｒ ₂ −ＯＨ（式中、Ｒ ₁ は置換または非置換のアルキル基、アルケニル基またはアリール基からなる群から選択され、そしてＲ ₂ はアルキル基およびアルコキシ基からなる群から選択される）を有するアルコールのホスフェートエステルである、上記［１］〜［１２］のいずれかに記載の流体組成物。
［１５］ Ｒ ₁ が少なくとも２個の炭素原子を有する、上記［１４］に記載の流体組成物。
［１６］ Ｒ ₁ が３０個以下の炭素原子を有する、上記［１４］または［１５］に記載の流体組成物。
［１７］ Ｒ ₁ が、アルキル置換されたアリール基である、上記［１４］〜［１６］のいずれかに記載の流体組成物。
［１８］ Ｒ ₂ がエトキシ基である、上記［１４］〜［１７］のいずれかに記載の流体組成物。
［１９］ Ｒ ₁ が、非置換のアルケニル基である、上記［１４］〜［１６］および［１８］のいずれかに記載の流体組成物。
［２０］ 少なくとも１種のホスフェートエステルが、流体組成物の約０．０５質量％以上の量で存在する、上記［１］〜［１９］のいずれかに記載の流体組成物。
［２１］ 少なくとも１種のホスフェートエステルが、流体組成物の約０．４質量％以下の量で存在する、上記［１］〜［２０］のいずれかに記載の流体組成物。
［２２］ 式：
Ｒ ₇ −（Ｏ−（ＰＯ） _m （ＥＯ） _n −Ｒ ₈ ） _x
（式中、ＰＯは、プロピレンオキサイド単位であり；
ＥＯは、エチレンオキサイド単位であり；
Ｒ ₇ は、水素またはｘ価ヒドロカルビル基であり；
ｘは、少なくとも１であり；
Ｒ ₈ は、水素またはヒドロカルビル基であり；
ｍは、少なくとも０の数であり；
ｎは、少なくとも０の数であり；そして
ｍ＋ｎは、０超である。）
を有するポリアルキレングリコールを更に含む、上記［１］〜［２１］のいずれかに記載の流体組成物。
［２３］ ｍ＝ｎである、上記［２２］に記載の流体組成物。
［２４］ 流体組成物の平衡還流沸点が少なくとも約２３０℃である、上記［１］〜［２３］のいずれかに記載の流体組成物。
［２５］ 流体組成物の動粘度が、−４０℃にて約１８００ｃＳｔ以下である、上記［１］〜［２４］のいずれかに記載の流体組成物。
［２６］ 組成物を水および塩化物塩と組合せて、水が総組成物の５体積％の量で存在しかつ塩化物イオンが総組成物の１００万分の２５質量部の量で存在する総組成物を得たときに、該総組成物が、ＳＡＥ基準Ｊ１７０４］に記載される錫めっき鉄、鋼、アルミニウム、鋳鉄、真鍮および銅についての最大許容質量変化仕様に適合する、上記［１］〜［２５］のいずれかに記載の流体組成物。
［２７］ 流体組成物を、ポリアミド６６および４３質量％ガラス繊維とのコンポジットを含む第１の表面と、ショアＡ硬度８０を有するＥＰＤＭゴムを含む第２の表面との間に適用し、そして該第１の表面が摺動自在に第２の表面を係合したときに、該第１の表面と該第２の表面との間の１００秒間の摺り係合の後の摩擦係数が０．０７未満である、上記［１］〜［２６］のいずれかに記載の流体組成物。
［２８］ ボアを有するマスターシリンダーを含み、上記［１］〜［２７］のいずれかに記載の流体組成物が該ボア内に配置されている、ブレーキシステム。
［２９］ マスターシリンダーが、ボアを規定する内側表面を有し、そして該内側表面がプラスチックライニングを有する、上記［２８］に記載のブレーキシステム。
［３０］ プラスチックライニングがポリアミドを含む、上記［２９］に記載のブレーキシステム。
［３１］ 少なくとも１種のグリコールおよび添加剤パッケージを含む流体組成物であって、流体組成物を、ポリアミド６６および４３質量％ガラス繊維とのコンポジットを含む第１の表面と、ショアＡ硬度８０を有するＥＰＤＭゴムを含む第２の表面との間に適用し、そして該第１の表面が摺動自在に第２の表面を係合したときに、該第１の表面と該第２の表面との間の１００秒間の摺り係合の後の摩擦係数が約０．０７未満である、流体組成物。
［３２］ 該第１の表面と該第２の表面との間の１００秒間の摺り係合の後の摩擦係数が、約０．０３未満である、上記［３１］に記載の流体組成物。
［３３］ 流体組成物の平衡還流沸点が少なくとも約２３０℃である、上記［３１］または［３２］に記載の流体組成物。
［３４］ 組成物の動粘度が、−４０℃にて約１８００ｃＳｔ以下である、上記［３１］〜［３３］のいずれかに記載の流体組成物。
［３５］ 組成物を水および塩化物塩と組合せて、水が総組成物の５体積％の量で存在しかつ塩化物イオンが総組成物の１００万分の２５質量部の量で存在する総組成物を得たときに、該総組成物が、ＳＡＥ基準Ｊ１７０４］に記載される錫めっき鉄、鋼、アルミニウム、鋳鉄、真鍮および銅についての最大許容質量変化仕様に適合する、上記［３１］〜［３４］のいずれかに記載の流体組成物。
［３６］ 少なくとも１種のグリコールが、式：

（式中、Ｒ ₁ 、Ｒ ₂ 、Ｒ ₃ 、Ｒ ₄ およびＲ ₅ は独立に、水素、および１〜８個の炭素原子を含有するアルキル基からなる群から選択され、そしてｎは少なくとも１である。）
を有する、上記［３１］〜［３５］のいずれかに記載の流体組成物。
［３７］ 少なくとも１種のグリコールが、ｎ＝２である第１のグリコール成分と、ｎ＝３である第２のグリコール成分とを含む、上記［３６］に記載の流体組成物。
［３８］ 少なくとも１種のグリコール成分が、Ｒ ₁ が１個の炭素原子を含有するアルキル基である第１のグリコール成分と、Ｒ ₁ が４個の炭素原子を含有するアルキル基である第２のグリコール成分とを含む、上記［３６］または［３７］に記載の流体組成物。
［３９］ 流体組成物の約７０質量％以下の量で存在する少なくとも１種のグリコールボレートエステルを更に含む、上記［３１］〜［３８］のいずれかに記載の流体組成物。
［４０］ 式：
Ｒ ₇ −（Ｏ−（ＰＯ） _m （ＥＯ） _n −Ｒ ₈ ） _x
（式中、ＰＯは、プロピレンオキサイド単位であり；
ＥＯは、エチレンオキサイド単位であり；
Ｒ ₈ は、水素またはヒドロカルビル基であり；
ｘは、少なくとも１であり；
Ｒ ₇ は、水素またはｘ価ヒドロカルビル基であり；
ｍは、少なくとも０の数であり；
ｎは、少なくとも０の数であり；そして
ｍ＋ｎは、０超である。）
を有する、少なくとも１種のポリアルキレングリコールを更に含む、上記［３１］〜［３９］のいずれかに記載の流体組成物。
［４１］ ｍ＝ｎである、上記［４０］に記載の流体組成物。
［４２］ 添加剤パッケージが、少なくとも１種の脂肪酸および少なくとも１種のホスフェートエステルを含む、上記［３１］〜［４１］のいずれかに記載の流体組成物。
［４３］ ボアを有するマスターシリンダーを含み、上記［３１］〜［４２］のいずれかに記載の流体組成物が該ボア内に配置されている、ブレーキシステム。
［４４］ マスターシリンダーが、ボアを規定する内側表面を有し、そして該内側表面がプラスチックライニングを有する、上記［４３］に記載のブレーキシステム。
［４５］ プラスチックライニングがポリアミドコンポジットを含む、上記［４４］に記載のブレーキシステム。 The description and illustrations provided herein are intended to introduce other persons skilled in the art to the disclosure, its principles, and its practical application. Those skilled in the art can adapt and apply the disclosure in its many forms to best suit the requirements of a particular application. Accordingly, the specific aspects of the disclosure described are not intended to be exclusive or limiting. Accordingly, the scope of the disclosure should be determined not with reference to the above description, but with reference to the appended claims, along with the full range of equivalents to which such claims are entitled. The disclosures of all articles and literature (eg patent applications and publications) are incorporated by reference in their entirety.
The present invention has the following aspects.
[1] at least one glycol; and
An additive package comprising at least one fatty acid and a phosphate ester;
A fluid composition comprising:
[2] The fluid composition of [1] above, wherein the at least one glycol is present in an amount greater than about 20% by weight of the total fluid composition.
[3] The fluid composition of [1] or [2] above, wherein the at least one glycol is present in an amount of less than about 99% by weight of the total fluid composition.
[4] At least one glycol has the formula:

Wherein R ₁ , R ₂ , R ₃ , R ₄ and R ₅ are independently selected from the group consisting of hydrogen and alkyl groups containing 1 to 8 carbon atoms, and n is at least 1 is there.)
The fluid composition according to any one of the above [1] to [3].
[5] The fluid composition according to the above [4], wherein the at least one glycol includes a first glycol component in which n = 2 and a second glycol component in which n = 3.
[6] At least one glycol component is a _first glycol component in which R ₁ is an alkyl group containing 1 carbon atom, and a second glycol component in which R ₁ is an alkyl group containing 4 carbon atoms. The fluid composition according to the above [4] or [5], comprising a glycol component.
[7] The fluid composition of any of the above-mentioned [1]-[6], further comprising at least one glycol borate ester present in an amount that is less than about 70% by weight of the fluid composition.
[8] The fluid composition according to any of [1] to [7] above, wherein the additive package is present in an amount that is less than about 10% by weight of the fluid composition.
[9] The fluid composition according to any of [1] to [8] above, wherein the additive package is present in an amount that is greater than about 0.1% by weight of the fluid composition.
[10] The fluid composition according to any one of [1] to [9], wherein the at least one fatty acid is linear.
[11] The fluid composition according to any one of [1] to [10], wherein at least one fatty acid is monounsaturated.
[12] The fluid composition according to any one of [1] to [11] above, wherein the at least one fatty acid is present in an amount of at least about 0.01% by mass of the fluid composition.
[13] The fluid composition according to any one of the above [1] to [12], wherein the fatty acid is present in an amount of about 0.4% or less of the fluid composition.
[14] The phosphate ester is of the formula R ₁ —R ₂ —OH, wherein R ₁ is selected from the group consisting of substituted or unsubstituted alkyl, alkenyl or aryl groups, and R ₂ is alkyl and alkoxy The fluid composition according to any one of the above [1] to [12], which is a phosphate ester of alcohol having (selected from the group consisting of groups).
[15] The fluid composition according to the above [14], wherein R ₁ has at least 2 carbon atoms.
[16] The fluid composition according to the above [14] or [15], wherein R ₁ has 30 or less carbon atoms.
[17] The fluid composition according to any one of the above [14] to [16], wherein R ₁ is an alkyl-substituted aryl group.
[18] The fluid composition according to any one of [14] to [17], wherein R ₂ is an ethoxy group.
[19] The fluid composition according to any one of [14] to [16] and [18], wherein R ₁ is an unsubstituted alkenyl group.
[20] The fluid composition according to any one of the above [1] to [19], wherein the at least one phosphate ester is present in an amount of about 0.05% by mass or more of the fluid composition.
[21] The fluid composition according to any one of the above [1] to [20], wherein the at least one phosphate ester is present in an amount of about 0.4% by mass or less of the fluid composition.
[22] Formula:
_{R 7 - (O- (PO)} m (EO) n -R 8) x
(Wherein PO is a propylene oxide unit;
EO is an ethylene oxide unit;
R ₇ is hydrogen or an x-valent hydrocarbyl group;
x is at least 1;
R ₈ is hydrogen or a hydrocarbyl group;
m is a number of at least 0;
n is a number of at least 0; and
m + n is greater than zero. )
The fluid composition according to any one of the above [1] to [21], further comprising a polyalkylene glycol having:
[23] The fluid composition according to the above [22], wherein m = n.
[24] The fluid composition according to any one of [1] to [23] above, wherein the fluid composition has an equilibrium reflux boiling point of at least about 230 ° C.
[25] The fluid composition according to any one of [1] to [24], wherein the fluid composition has a kinematic viscosity of about 1800 cSt or less at −40 ° C.
[26] Combining the composition with water and a chloride salt, a total of water present in an amount of 5% by volume of the total composition and chloride ions present in an amount of 25 parts per million by weight of the total composition. When the composition is obtained, the total composition meets the maximum allowable mass change specification for tinned iron, steel, aluminum, cast iron, brass and copper as described in SAE Standard J1704] [1] -Fluid composition in any one of [25].
[27] A fluid composition is applied between a first surface comprising a composite of polyamide 66 and 43% by weight glass fiber and a second surface comprising EPDM rubber having a Shore A hardness of 80, and When the first surface slidably engages the second surface, the coefficient of friction after 100 seconds of sliding engagement between the first surface and the second surface is 0.07. The fluid composition according to any one of [1] to [26], which is less than
[28] A brake system comprising a master cylinder having a bore, wherein the fluid composition according to any one of [1] to [27] is disposed in the bore.
[29] The brake system of [28] above, wherein the master cylinder has an inner surface defining a bore, and the inner surface has a plastic lining.
[30] The brake system according to [29], wherein the plastic lining includes polyamide.
[31] A fluid composition comprising at least one glycol and additive package, the fluid composition comprising a first surface comprising a composite of polyamide 66 and 43% by weight glass fiber, and a Shore A hardness of 80 The first surface and the second surface when applied between the second surface including the EPDM rubber and having the first surface slidably engage the second surface. A fluid composition wherein the coefficient of friction after 100 seconds of sliding engagement is less than about 0.07.
[32] The fluid composition according to [31], wherein the coefficient of friction after 100 seconds of sliding engagement between the first surface and the second surface is less than about 0.03.
[33] The fluid composition according to [31] or [32] above, wherein the fluid composition has an equilibrium reflux boiling point of at least about 230 ° C.
[34] The fluid composition according to any one of [31] to [33], wherein the composition has a kinematic viscosity of about 1800 cSt or less at −40 ° C.
[35] combining the composition with water and a chloride salt, wherein the water is present in an amount of 5% by volume of the total composition and the chloride ion is present in an amount of 25 parts per million by weight of the total composition. [31] above, when the composition is obtained, the total composition meets the maximum allowable mass change specifications for tinned iron, steel, aluminum, cast iron, brass and copper as described in SAE Standard J1704] -The fluid composition in any one of [34].
[36] At least one glycol is of the formula:

Wherein R ₁ , R ₂ , R ₃ , R ₄ and R ₅ are independently selected from the group consisting of hydrogen and alkyl groups containing 1 to 8 carbon atoms, and n is at least 1 is there.)
The fluid composition according to any one of the above [31] to [35].
[37] The fluid composition according to [36], wherein the at least one glycol includes a first glycol component in which n = 2 and a second glycol component in which n = 3.
[38] At least one glycol component is a _first glycol component in which R ₁ is an alkyl group containing 1 carbon atom and a second glycol component in which R ₁ is an alkyl group containing 4 carbon atoms. The fluid composition according to [36] or [37] above, comprising a glycol component of
[39] The fluid composition according to any of [31] to [38], further comprising at least one glycol borate ester present in an amount of about 70% by mass or less of the fluid composition.
[40] Formula:
_{R 7 - (O- (PO)} m (EO) n -R 8) x
(Wherein PO is a propylene oxide unit;
EO is an ethylene oxide unit;
R ₈ is hydrogen or a hydrocarbyl group;
x is at least 1;
R ₇ is hydrogen or an x-valent hydrocarbyl group;
m is a number of at least 0;
n is a number of at least 0; and
m + n is greater than zero. )
The fluid composition according to any one of the above [31] to [39], further comprising at least one polyalkylene glycol having:
[41] The fluid composition according to [40], wherein m = n.
[42] The fluid composition according to any one of [31] to [41], wherein the additive package includes at least one fatty acid and at least one phosphate ester.
[43] A brake system comprising a master cylinder having a bore, wherein the fluid composition according to any one of [31] to [42] is disposed in the bore.
[44] The brake system of [43] above, wherein the master cylinder has an inner surface defining a bore, and the inner surface has a plastic lining.
[45] The brake system according to [44], wherein the plastic lining includes a polyamide composite.

Claims (15)

An additive package comprising at least one glycol; and at least one fatty acid and a phosphate ester;
Wherein the at least one glycol is present in an amount greater than 80 % by weight of the total fluid composition, the phosphate ester comprises dinonylphenol ethoxylated phosphate ester, and the fatty acid is from 15 to 25 carbons. A fluid composition comprising atoms . The fluid composition, a) was applied between a first surface comprising a composite of polyamide 66 and b) 43 wt% glass textiles, and a second surface comprising EPDM rubber having a Shore A hardness of 80, and When the first surface slidably engages the second surface, the coefficient of friction after 100 seconds of sliding engagement between the first surface and the second surface is 0. The fluid composition of claim 1, wherein the fluid composition is less than 07. The fluid composition of claim 2 , wherein the coefficient of friction after 100 seconds of sliding engagement between the first surface and the second surface is less than 0.03.   The fluid composition of claim 1, wherein the at least one fatty acid is linear.   The fluid composition of claim 1, wherein the at least one fatty acid is monounsaturated. The phosphate ester is of the formula R ₁ —R ₂ —OH
Wherein R ₁ is selected from the group consisting of substituted or unsubstituted alkyl groups, alkenyl groups and aryl groups, and R ₂ is selected from the group consisting of alkyl groups and alkoxy groups.
The fluid composition of claim 1, wherein the fluid composition is a phosphate ester of an alcohol having the formula: The fluid composition of claim 6 , wherein R ₁ has at least 2 carbon atoms. The fluid composition of claim 6 , wherein R ₁ is an alkyl substituted aryl group. The fluid composition according to claim 6 , wherein R ₂ is an ethoxy group. The fluid composition according to claim 6 , wherein R ₁ is an unsubstituted alkenyl group. At least one glycol has the formula:

Wherein R ₁ , R ₂ , R ₃ , R ₄ and R ₅ are independently selected from the group consisting of hydrogen and alkyl groups containing 1 to 8 carbon atoms, and n is at least 1 is there.)
The fluid composition according to claim 1 or 2 , wherein: The fluid composition of claim 11 , wherein the at least one glycol comprises a first glycol component where n = 2 and a second glycol component where n = 3. A first glycol component wherein R ₁ is an alkyl group containing 1 carbon atom and a second glycol component wherein R ₁ is an alkyl group containing 4 carbon atoms. The fluid composition of claim 11 , comprising: The fluid composition of claim 1 or 2 , further comprising at least one glycol borate ester present in an amount that is less than 10 % by weight of the fluid composition. formula:
_{R 7 - (O- (PO)} m (EO) n -R 8) x
(Wherein PO is a propylene oxide unit;
EO is an ethylene oxide unit;
R ₇ is hydrogen or an x-valent hydrocarbyl group;
x is at least 1;
R ₈ is hydrogen or a hydrocarbyl group;
m is a number of at least 0;
n is a number of at least 0; and m + n is greater than 0. )
The fluid composition of claim 1 or 2 , further comprising a polyalkylene glycol having:

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