Classifications

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  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
  • C10M141/06—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic nitrogen-containing compound
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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
  • C10M129/42—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms polycarboxylic
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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
  • C10M129/68—Esters
  • C10M129/72—Esters of polycarboxylic acids
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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
  • C10M129/68—Esters
  • C10M129/76—Esters containing free hydroxy or carboxyl groups
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  • C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
  • C10M129/86—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of 30 or more atoms
  • C10M129/92—Carboxylic acids
  • C10M129/93—Carboxylic acids having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
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  • C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
  • C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
  • C10M133/16—Amides; Imides
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  • C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
  • C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
  • C10M133/38—Heterocyclic nitrogen compounds
  • C10M133/44—Five-membered ring containing nitrogen and carbon only
  • C10M133/46—Imidazoles
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/10—Carboxylix acids; Neutral salts thereof
  • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
  • C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
  • C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • 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
  • C10M2207/127—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 polycarboxylic
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/10—Carboxylix acids; Neutral salts thereof
  • C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
  • C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/10—Carboxylix acids; Neutral salts thereof
  • C10M2207/22—Acids obtained from polymerised unsaturated acids
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  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/28—Esters
  • C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/28—Esters
  • C10M2207/285—Esters of aromatic polycarboxylic acids
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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  • C10M2207/287—Partial esters
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/28—Esters
  • C10M2207/287—Partial esters
  • C10M2207/288—Partial esters containing free carboxyl groups
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/28—Esters
  • C10M2207/287—Partial esters
  • C10M2207/289—Partial esters containing free hydroxy groups
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  • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
  • C10M2207/28—Esters
  • C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
• • C—CHEMISTRY; METALLURGY
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  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
  • C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/08—Amides
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/08—Amides
  • C10M2215/082—Amides containing hydroxyl groups; Alkoxylated derivatives
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/086—Imides
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  • C10M2215/12—Partial amides of polycarboxylic acids
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/12—Partial amides of polycarboxylic acids
  • C10M2215/122—Phtalamic acid
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/22—Heterocyclic nitrogen compounds
  • C10M2215/223—Five-membered rings containing nitrogen and carbon only
  • C10M2215/224—Imidazoles
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/26—Amines
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  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2215/28—Amides; Imides
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  • C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • C10M2217/042—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds between the nitrogen-containing monomer and an aldehyde or ketone
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  • C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • C10M2217/043—Mannich bases
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  • C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
  • C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
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  • C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2040/00—Specified use or application for which the lubricating composition is intended
  • C10N2040/08—Hydraulic fluids, e.g. brake-fluids

Definitions

• the present invention relates to lubricating compositions which exhibit good rust inhibition and wet filterability and to their use.
• Fluids/lubricants for turbine (“R&O"), hydraulic and industrial applications are required to meet a variety of performance characteristics and these tend to be achieved by blending an additive/additive pack with a base oil.
• the additive/additive pack imparts the desired properties to the base oil thereby making it suitable for its intended utility.
• Rust inhibition is a property which is often desired, particularly in'hydraulic fluids and turbine oils, and numerous additives have been used to achieve this.
• acidic rust inhibitors such as reaction products of carboxylic acids, polyalkylene polyamines and alkenyl succinic anhydrides such as are described in USP 4,101,429.
• acidic rust inhibitors can give the desired level of rust inhibition, in the presence of water they tend also to interact with metals which may be present either deliberately, in the form of other functional additives components such as metal-containing detergents, or as contaminants. This interaction can lead to the production of degredation products leading to deposit formation as particulates and/or precipitates.
• the degradation product are particularly troublesome because to maintain good power transmission and to avoid damaging hydraulic equipment in which they are used, the hydraulic fluid should be kept meticulously clean and free of contaminants. To ensure that the fluid is substantially free of contaminants very fine filters are used. However, the kind of degredation products which are produced can result in filter clogging or blocking.
• Turbine oils represent another practical situation where the cleanliness of the lubricant (R&O oil) used is important. To maintain effective operating conditions and to avoid damaging the equipment in which they are used turbine oils should be kept meticulously clean and free of contaminants. Again, very fine filters are used to minimize contamination.
• R&O oil lubricant
• the present invention provides a lubricant composition which exhibits rust performance comparable to compositions based on the kind of acidic rust inhibitors mentioned above, and which do not interact adversely with metal(s) which are present in the formulated lubricant, especially when water is also present, i.e. the compositions exhibit good wet filterability. It is also desirable to provide a rust inhibitor system which has good solubility in a variety of oil basestocks. The present invention also satisfies this criterion.
• the present invention provides a lubricant composition
• a lubricant composition comprising a base oil, a rust inhibitor system comprising (A) at least one neutral rust inhibitor and (B) a compound of formula: in which Z is a group R 1 R 2 CH-, in which R 1 and R 2 are each independently hydrocarbyl groups containing up to 34 carbon atoms, the total number of carbon atoms in the groups R 1 and R 2 being from 11 to 35, and (C) a solubilising agent for the rust inhibitor system which is an ashless dispersant.
• neutral rust inhibitor in the present specification, means a rust inhibitor that is essentially free of -COOH functional groups.
• the at least one neutral rust inhibitor is a hydrocarbyl ester of formula R(COOR') n in which R and R' are each independently hydrocarbyl or hydroxyhydrocarbyl groups containing up to about 40 carbon atoms and n is from 1 to 4.
• R and R' are each independently hydrocarbyl groups, or hydroxyhydrocarbyl groups, containing 8 to 20 carbon atoms, and n is from 1 to 4.
• the maximum number of groups COOR' which are present on the hydrocarbyl or hydroxyhydrocarbyl group R will vary depending on the number of carbon atoms in R. For example, if R is a hydrocarbyl group containing only one carbon atom, the maximum possible value of n will be 4. When R is a hydroxyhydrocarbyl group containing one carbon atom the maximum value of n will be 3.
• the hydrocarbyl esters can be prepared by conventional esterification procedures from a suitable alcohol and an acid, acid halide, acid anhydride or mixtures thereof. Also, the esters of the invention can be prepared by conventional methods of transesterification. By “essentially free”, it is meant that the starting acids, acid halides, acid anhydrides or mixtures thereof used in preparing the hydrocarbyl esters are reacted with an amount of alcohol sufficient to theoretically convert all of the -COOH groups to esters. Typically, the ester will have a TAN of less than 10mgKOH/g.
• Preferred esters include, but are not limited to, octyloleyl malate, dioleylmalate, pentaerythritol monooleate and glycerol monooleate. Of these the use of pentaerythritol monooleate is more preferred.
• Another class of preferred neutral rust inhibitors includes aspartic acid diesters of 1-(2-hydroxyethyl-2-heptadecenyl)-imidazoline.
• This imidazoline is primarily a mixture of diester of L-aspartic acid and an imidazoline based on the reaction between oleic acid and ethanolamine.
• Esters of this type are commercially available from Mona Industries, Inc. as Monacor R 39.
• the radical Z may be, for example, 1-methylpentadecyl, 1-propyltridecenyl, 1-pentyltridecenyl, 1-tridecenylpentadecenyl or 1-tetradecyleicosenyl.
• the number of carbon atoms in the groups R 1 and R 2 is from 16 to 28 and more commonly 18 to 24. It is especially preferred that the total number of carbon atoms in R 1 and R 2 is about 20 to 22.
• the preferred compound (B) is a 3-C 18-24 alkenyl-2,5-pyrrolidindione, i.e. a compound in which the average number of carbon atoms in the alkenyl group is from 18 to 24.
• the compound (B) has a titratable acid number (TAN) of about 80 to about 140 mgKOH/g, preferably about 110mgKOH/g.
• TAN titratable acid number
• the compounds (B) are commercially available or may be made by the application or adaptation of known techniques (see for example EP-A-0389237).
• Component (C) is an ashless dispersant.
• the ashless dispersant may be a hydrocarbyl succinimide, i.e. the reaction product of a polyamine, such as a polyalkylene polyamine, and a hydrocarbyl succinic acylating agent.
• succinimide is intended to encompass compounds which many have an amide, amidine and/or salt linkage in addition to the imide linkage that results from the reaction mentioned.
• succinimides preferred are those in which one of the reactants is an aliphatic hydrocarbyl substituted succinic acylating agent in which the hydrocarbyl moiety contains at least 40 carbon atoms.
• the hydrocarbyl moiety is derived from a polyalkene.
• Useful polyalkenes normally have a number average molecular weight of from about 500 to about 10000, for example from about 950 to about 5000.
• the polyalkene itself may be derived from an ethylenically unsaturated monomer such as ethylene, propylene, 1-butene, isobutene and 1-octene, or polyolefinic monomers such as 1,3-butadiene or isoprene.
• the polyalkene is polyisobutene.
• the succinic groups of the acylating agent are usually derived from maleic acid or maleic anhydride or fumaric acid.
• the acylating agent is a polyisobutenyl succinic acid or anhydride.
• the polyalkylene polyamine may be represented by the formula H 2 N(CH 2 ) n (NH(CH 2 ) n ) m NH 2 in which n is 2 to about 10 (preferably 2 to 4, most preferably 2) and m is 0 to 10, preferably about 1 to 6.
• Examples include ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, spermine, pentaethylene hexamine, propylene diamine, butylene diamine, hexamethylene diamine and decamethylene diamine. Mixtures of amines may be used.
• Another useful type of polyamine comprises a mixture of acyclic hydrocarbyl polyamines and hydrocarbyl cyclic polyamines.
• the use of such amines, as well of those mentioned earlier are specifically disclosed in EP-A-0460309.
• the latter describes useful ashless dispersants of this type and their preparation. Useful dispersants are also commercially available.
• useful dispersants may also be formed by reacting the acylating agent with organic hydroxy compounds such as phenols and alcohols, and/or basic inorganic materials. Such dispersants are also well-known in the art (for example, USP 4,466,894).
• the ashless dispersant may be a so-called "Mannich dispersant". These are the reaction products of alkyl phenols, in which the alkyl group typically contains at least about 30 carbon atoms with aldehydes, especially formaldehyde, and amines, such as polyalkylene polyamines. These dispersants are also well-known in the art (for example, USP 3,413,347, USP 3,697,574, USP 3,725,277, USP 3,725,480 and USP 3,726,882).
• the ashless dispersant may be the reaction product of a high molecular weight hydrocarbyl halide with an amine.
• These dispersants are known in the art and described in such documents as USP 3,454,555 and USP 5,565,804.
• any of the aforementioned dispersants may be used in post-treated form, that is by subsequent reaction with one or more conventional post-treating agents.
• suitable post-treating agent include boron compounds, phosphorus compounds and acylating agents such as dibasic acylating agents. Suitable post-treatment is discussed in greater detail in, for example, EP-A-0460309.
• ashless dispersant which may be used, mention may be made of interpolymers of oil-solubilising monomers such as decyl methacrylate, vinyl decyl ether and high molecular weight olefins, with monomers containing polar substituents. These are also known in the art (for example, see USP 3,687,849 and USP 3,702,300).
• the composition further comprises, as component (D), an aliphatic carboxylic acid or anhydride in which the aliphatic group contains at least 20 carbon atoms.
• the group typically includes upto about 500 carbon atoms, preferably from about 10 to about 300 carbon atoms and often from about 10 to about 150 carbon atoms.
• component (D) may be an aliphatic substituted succinic anhydride or acid containing from about 20 to about 500 carbon atoms in the aliphatic substituent, preferably from about 30 to about 300 carbon atoms, and often from about 50 to about 150 carbon atoms.
• Patents describing useful aliphatic carboxylic acids or anhydrides and methods for preparing them include USP nos. 3,215,707, 3,219,666, 3,231,587, 3,912,764, 4,110,349 and 4,234,435 and GB 1,440,219.
• component (D) is an alkenyl carboxylic acid or anhydride in which the alkenyl group contains from 10 to 75 carbon atoms, preferably an alkenyl succinic anhydride in which the alkenyl group contains from 10 to 65 carbon atoms.
• component (D) may be a polyisobutenyl succinic anhydride in which the polyisobutenyl moiety has a number average molecular weight of about 300 to about 950. It has been found that component (D) provides further advantages in terms of component solubility.
• number average molecular weight is determined by mass spectral analysis.
• hydrocarbyl groups and moieties may be straight- or branched-chain.
• the compositions are substantially free of acidic rust inhibitors and/or metal detergents.
• substantially free means that no acidic rust inhibitors or metal, for example as metal-containing detergent, are purposefully added to the finished oil although there may be some present due to contamination or as an impurity.
• Lubricating oils contemplated for use in this invention include natural lubricating oils, synthetic lubricating oils and mixtures thereof. Suitable lubricating oils also include basestocks obtained by isomerization of synthetic wax and slack wax, as well as basestocks produced by hydrocracking (rather than solvent extracting) the aromatic and polar components of crude oil.
• both the natural and synthetic lubricating oils will each have a kinematic viscosity ranging from about 1 x 10 -6 m 2 /s to about 40 x 10 -6 m 2 /s (about 1 to about 40 cSt) at 100°C, although typical applications will require each oil to have a viscosity ranging from about 2 x 10 -6 m 2 /s to about 8 x 10 -6 m 2 /s (about 2 to about 8 cSt) at 100°C.
• Natural base oils include animal oils, vegetable oils (e.g., castor oil and lard oil), petroleum oils, mineral oils, and oils derived from coal or shale.
• the preferred natural base oil is mineral oil.
• the mineral oils useful in this invention include all common mineral oil base stocks. This would include oils that are naphthenic or paraffinic in chemical structure. Oils that are refined by conventional methodology using acid, alkali, and clay or other agents such as aluminum chloride, or they may be extracted oils produced, for example, by solvent extraction with solvents such as phenol, sulfur dioxide, furfural, dichlordiethyl ether, etc. They may be hydrotreated or hydro-refined, dewaxed by chilling or catalytic dewaxing processes, or hydrocracked. The mineral oil may be produced from natural crude sources or be composed of isomerized wax materials or residues of other refining processes.
• the mineral oils will have kinematic viscosities of from 2 x 10 -6 m 2 /s to 12 x 10 -6 m 2 /s (2 cSt to 12 cSt) at 100°C.
• the preferred mineral oils have kinematic viscosities of from 3 x 10 -6 m 2 /s to 10 x 10 -6 m 2 /s (3 to 10 cSt), and most preferred are those mineral oils with viscosities of 5 x 10 -6 m 2 /s to 9 x 10 -6 m 2 /s (5 to 9 cSt) at 100°C.
• Synthetic lubricating oils useful in this invention include hydrocarbon oils and halo-substituted hydrocarbon oils such as oligomerized, polymerized, and interpolymerized olefins [e.g., polybutylenes, polypropylenes, propylene, isobutylene copolymers, chlorinated polylactenes, poly(1-hexenes), poly(1-octenes), and mixtures thereof]; alkylbenzenes [e.g., polybutylenes, polypropylenes, propylene, isobutylene copolymers, chlorinated polylactenes, poly(1-hexenes), poly (1-octenes) and mixtures thereof]; alkylbenzenes [e.g., dodecyl-benzenes, tetradecylbenzenes, dinonylbenzenes and di(2-ethylhexyl)benzene]; polyphenyl
• Synthetic lubricating oils also include alkylene oxide polymers, interpolymers, copolymers, and derivatives thereof where the terminal hydroxyl groups have been modified by esterification or etherification.
• This class of synthetic oils is exemplified by: polyoxyalkylene polymers prepared by polymerization of ethylene oxide or propylene oxide; the alkyl and aryl ethers of these polyoxyalkylene polymers (e.g., methylpolyisopropylene glycol ether having an average molecular weight of 1000, diphenyl ether of polypropylene glycol having a molecular weight of 100-1500); and mono- and poly-carboxylic esters thereof (e.g., the acetic acid esters, mixed C 3 -C 8 fatty acid esters, and C 12 oxo acid diester of tetraethylene glycol).
• Another suitable class of synthetic lubricating oils comprises the esters of dicarboxylic acids (e.g., phthalic acid, succinic acid, alkyl succinic acids and alkenyl succinic acids, maleic acid, azelaic acid, suberic acid, sebacic acid, fumaric acid, adipic acid, linoleic acid dimer, malonic acid, alkylmalonic acids and alkenyl malonic acids) with a variety of alcohols (e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl alcohol, ethylene glycol, diethylene glycol monoethers and propylene glycol).
• dicarboxylic acids e.g., phthalic acid, succinic acid, alkyl succinic acids and alkenyl succinic acids, maleic acid, azelaic acid, suberic acid, sebacic acid, fumaric acid, adipic acid, lino
• esters include dibutyl adipate, di(2-ethylhexyl) sebacate, di-n-hexyl fumarate, dioctyl sebacate, diisooctyl azelate, diisodecyl azelate, dioctyl isophthalate, didecyl phthalate, dieicosyl sebacate, the 2-ethylhexyl diester of linoleic acid dimer, and the complex ester formed by reacting one mole of sebacic acid with two moles of tetraethylene glycol and two moles of 2-ethyl-hexanoic acid.
• a preferred type of oil from this class of synthetic oils are adipates of C 4 to C 12 alcohols.
• Esters useful as synthetic lubricating oils also include those made from C 5 to C 12 monocarboxylic acids and polyols and polyol ethers such as neopentyl glycol, trimethylolpropane pentaerythritol, dipentaerythritol and tripentaerythritol.
• Silicon-based oils (such as the polyalkyl-, polyaryl-, polyalkoxy-, or polyaryloxy-siloxane oils and silicate oils) comprise another useful class of synthetic lubricating oils. These oils include tetra-ethyl silicate, tetraisopropyl silicate, tetra-(2-ethylhexyl) silicate, tetra-(4-methyl-2-ethylhexyl) silicate, tetra-(p-tert-butylphenyl) silicate, hexa-(4-methyl-2-pentoxy)-disiloxane, poly(dimethyl)-siloxanes and poly (methylphenyl) siloxanes.
• oils include tetra-ethyl silicate, tetraisopropyl silicate, tetra-(2-ethylhexyl) silicate, tetra-(4-methyl-2-ethyl
• Other synthetic lubricating oils include liquid esters of phosphorus containing acids (e.g., tricresyl phosphate, trioctylphosphate, and diethyl ester of decylphosphonic acid), polymeric tetrahydrofurans and poly- ⁇ -olefins.
• liquid esters of phosphorus containing acids e.g., tricresyl phosphate, trioctylphosphate, and diethyl ester of decylphosphonic acid
• polymeric tetrahydrofurans e.g., tricresyl phosphate, trioctylphosphate, and diethyl ester of decylphosphonic acid
• polymeric tetrahydrofurans e.g., polymeric tetrahydrofurans and poly- ⁇ -olefins.
• the lubricating base oils may be derived from refined, re-refined oils, or mixtures thereof.
• Unrefined oils are obtained directly from a natural source or synthetic source (e.g., coal, shale, or tar sands bitumen) without further purification or treatment.
• Examples of unrefined oils include a shale oil obtained directly from a retorting operation, a petroleum oil obtained directly from distillation, or an ester oil obtained directly from an esterification process, each of which is then used without further treatment.
• Refined oils are similar to the unrefined oils except that refined oils have been treated in one or more purification steps to improve one or more properties.
• Suitable purification techniques include distillation, hydrotreating, dewaxing, solvent extraction, acid or base extraction, filtration, and percolation, all of which are known to those skilled in the art.
• Re-refined oils are obtained by treating used oils in processes similar to those used to obtain the refined oils. These re-refined oils are also known as reclaimed or reprocessed oils and are often additionally processed by techniques for removal of spent additives and oils breakdown products.
• White oils, as taught in U.S. 5,736,490 may also be used as the base oil, especially for turbine applications.
• Another aspect of the invention concerns the solubility of the active components of the lubricant compositions in a variety of types of base oil.
• the ashless dispersant (C) and, where present, compound (D) are responsible for the enhanced solubility of the rust inhibitor system, especially in hydroprocessed basestocks with reduced aromaticity and thus reduced solvency.
• One consequence of enhanced additive solubility is improved filterability.
• the invention also provides use of the ashless dispersant (C) and, optionally, compound (D) to improve aesthetic appearance of a base oil comprising the rust inhibitor system on contamination with water.
• the American Petroleum Institute has categorized these different basestock types as follows: Group I, >0.03 wt% sulfur, and/or ⁇ 90 vol% saturates, viscosity index between 80 and 120; Group II, ⁇ 0.03 wt% sulfur, and ⁇ 90 vol% saturates, viscosity index between 80 and 120; Group III, ⁇ 0.03 wt% sulfur, and ⁇ 90 vol% saturates, viscosity index >120; Group IV, all polyalphaolefins. Hydrotreated basestocks and catalytically dewaxed basestocks, because of their low sulfur and aromatics content, generally fall into the Group II and Group III categories.
• Polyalphaolefins (Group IV basestocks) are synthetic base oils prepared from various alpha olefins and are substantially free of sulfur and aromatics.
• the lubricant composition of the present invention may be prepared by simple blending of the various components with a suitable base oil.
• the additive components used in practice of this invention may be provided as a concentrate for formulation into a lubricant composition ready for use.
• the concentrate may comprise, in addition to the various components, a solvent or diluent for the fluid components.
• the solvent or diluent should be miscible with and/or capable of dissolving in the base oil to which the concentrate is to be added. Suitable solvents and diluents are well known.
• the solvent or diluent may be the base oil of the lubricating oil composition itself.
• the concentrate may suitably include any of the conventional additives used in lubricating oils compositions. The proportions of each component in the concentrate are controlled by the intended degree of dilution, though top treatment of the formulated fluid is possible.
• the weight ratio of components (A):(B) is usually from 3:1 to 8:1, preferably 4:1 to 6:1.
• the total amount of (A) and (B) should be present in the finished oil in an amount of 0.15 to 0.5% by weight, preferably from 0.20 to about 0.4% by weight.
• the weight ratio of [(A)+(B)]:(C) is usually 7.5:1, in the concentrate or finished oil.
• the total amount of (C) in the finished oil is usually 0.03% by weight.
• component (D) should be present in the finished oil in an amount of 0.01 % by weight.
• the amounts (A), (B), (C) and, where used, (D) in a concentrate are such that the amounts mentioned should be achieved in the finished composition when the concentrate is used at typical treat rates of, for instance, 0.30% by weight.
• additives commonly used in lubricants/fluids for turbine, hydraulic and industrial applications may be included in the compositions or concentrates of the present invention. These include antiwear agents, such as sulphur and/or phosphorus containing compounds, antioxidants, demulsifiers and corrosion inhibitors. These additives, when present, are used in amounts conventionally used in such applications. Some additives may be included in the concentrate and some added to the fully formulated lubricant/fluid as a top-treat.
• Lubricant fluid compositions were prepared in accordance with the following table. The amounts given for each component are expressed as percentage by weight of component in an additive concentrate. The treat rate indicates the level of dilution of the concentrate in formulating the composition.
• the compatibility of the additive components in the compositions was assessed visually after one month.
• each fluid was assessed using Afnor E48-691 (wet) test.
• Afnor E48-691 wet test.
• a water-treated fluid is filtered under conditions of constant pressure and temperature through a membrane with a determined absolute stopping power.
• the IF ratio therefore consists of comparing the filtration speeds of the fluid in the course of the test.
• the ratio as well as the filtration speed of the various segments for each sample are indicative of the ease of filtration of the fluid.
• An IF value of less than 1 indicates a fault in the test method. The closer the IF value to 1, the better filtrability of the fluid. If during testing the membrane becomes clogged an abort result is recorded.
• the Shell Filtration Test is used to evaluate the filterability characteristics of oil based hydraulic fluids with and without calcium and/or water contamination.
• the fluids as blended and the contaminated fluids are each tested in duplicate as follows. After pre-treatment at 70°C, 300 ml of test oil are filtered through a 1.2 micron Millipore membrane using a 650 mm Hg vacuum. The fluid temperature is not specifically controlled but should be in the range of 19 to 26°C. The time in seconds for each successive 100 ml of fluid to filter, or for the filter membrane to block, are noted.
• the results of the Shell Filtration Test are indicated as either PASS, meaning that all 300 ml of oil passed through the filter, or FAIL, meaning that the filter became blocked.
• test fluid The tendency of the hydraulic fluid to cause rusting was assessed during the ASTM D665B test.
• a steel blank is cleaned by rotation at 1700 rpm in contact with 150 grade aluminium oxide cloth and then with 280 grade cloth.
• a PTFE holder is attached to the blank and this assembly completely immersed in a test tube containing the fluid under test.
• 300 ml of test fluid is poured into a 400 ml beaker, the beaker having been cleaned first using detergent solution, rinsed with distilled water and dried in an oven for about 15 minutes.
• the beaker is then placed in an oil bath (set to 60°C) to which a perspex cover is attached.
• a stirrer is lowered into the test fluid through a hole in the top of the cover and the fluid stirred.
• the steel blank is removed from the test tube and allowed to drain briefly before placing into the beaker. After a further 30 minutes, 30 ml of synthetic sea water solution is added to the test fluid in the beaker. After 24 hours the steel blank is removed from the test fluid, allowed to drain, rinsed with heptane and assessed according to the following rating system:
• the Group III basestock was Yubase 6.

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• 1999
  • 1999-07-30 EP EP99306079A patent/EP1078977B1/de not_active Expired - Lifetime
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• 2000
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