Classifications

• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
  • C10M135/32—Heterocyclic sulfur, selenium or tellurium compounds
  • C10M135/36—Heterocyclic sulfur, selenium or tellurium compounds the ring containing sulfur and carbon with nitrogen or oxygen
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • 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
  • C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
  • C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
  • C10M2215/28—Amides; Imides
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
  • C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
  • C10M2219/022—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of hydrocarbons, e.g. olefines
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
  • C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
  • C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
  • C10M2219/106—Thiadiazoles
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
  • C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
  • C10M2223/04—Phosphate esters
  • C10M2223/043—Ammonium or amine salts thereof
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
  • C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
  • C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
  • C10M2223/04—Phosphate esters
  • C10M2223/047—Thioderivatives not containing metallic elements
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2010/00—Metal present as such or in compounds
  • C10N2010/04—Groups 2 or 12
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2010/00—Metal present as such or in compounds
  • C10N2010/08—Groups 4 or 14
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2010/00—Metal present as such or in compounds
  • C10N2010/10—Groups 5 or 15
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2010/00—Metal present as such or in compounds
  • C10N2010/12—Groups 6 or 16
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
  • C10N2030/40—Low content or no content compositions
  • C10N2030/42—Phosphor free or low phosphor content compositions
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
  • C10N2030/40—Low content or no content compositions
  • C10N2030/43—Sulfur free or low sulfur content compositions
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
  • C10N2030/54—Fuel economy
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2040/00—Specified use or application for which the lubricating composition is intended
  • C10N2040/02—Bearings
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2040/00—Specified use or application for which the lubricating composition is intended
  • C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
  • C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
  • C10N2060/14—Chemical after-treatment of the constituents of the lubricating composition by boron or a compound containing boron

Definitions

• a lubricant solution that can minimize power loss and operating temperature resulting in improved fluid efficiency would be technically and commercially beneficial.
• One aspect of the technology is therefore directed to an automotive or industrial gear oil comprising an oil of lubricating viscosity, and from 0.05 to 2 wt% of a reaction product of dimercaptodithiadiazole and at least one a, P-unsaturated carbonyl compound, or metal salt thereof.
• the formulation can also include an amine alkyl(thio)phosphate.
• the amine alkyl(thio)phosphate can be simply an amine alkylphosphate.
• the amine alkyl(thio)phosphate can be an amine alkylthiophosphate.
• the amine alkyl(thio)phosphate can include a combination of both amine phosphate and amine alkylthiophosphate.
• the lubricant can include an amine phosphate that is a substantially sulfur-free alkyl phosphate amine salt having at least about 30 mole percent of the phosphorus atoms in an alkyl pyrophosphate salt structure.
• At least about 80 mole percent of the alkyl groups in such a sulfur-free alkyl phosphate can be secondary alkyl groups of about 3 to about 12 carbon atoms. In some embodiments, at least about 25 mole percent of the alkyl groups in such a sulfur-free alkyl phosphate can be primary alkyl groups of about 3 to about 12 carbon atoms.
• the lubricant can also include a sulfurized olefin.
• the automotive or industrial gear oil can also contain other additives.
• the automotive or industrial gear oil can include other sulfur containing additives in an amount to provide the composition with a total sulfur level of about 0.75 to about 5 wt%.
• the automotive or industrial gear oil can have a total phosphorus level of about 0.01 to about 0.5 wt%.
• Another aspect of the technology encompasses a method of lubricating a driveline power transmitting device by supplying to the driveline power transmitting device an automotive or industrial gear oil as described, and operating the driveline power transmitting device.
• the driveline power transmitting device can be, for example, an axle, a bearing, a transmission or a gear.
• One aspect of the invention is an automotive or industrial gear oil containing (a) an oil of lubricating viscosity, (b) a DMTD derivative as taught herein, and optionally (c) sulfurized olefin or mixtures thereof, and (d) amine al- kyl(thio)phosphate.
• the base oil may be selected from any of the base oils in Groups I-V of the American Petroleum Institute (API) Base Oil Interchangeability Guidelines (2011), namely
• Group I >0.03 and/or ⁇ 90 80 to less than 120
• Group II ⁇ 0.03 and >90 80 to less than 120
• Groups I, II and III are mineral oil base stocks. Other generally recognized categories of base oils may be used, even if not officially identified by the API: Group II+, referring to materials of Group II having a viscosity index of 110-119 and lower volatility than other Group II oils; and Group III+, referring to materials of Group III having a viscosity index greater than or equal to 130.
• the oil of lubricating viscosity can include natural or synthetic oils and mixtures thereof. Mixtures of mineral oil and synthetic oils, e.g., polyalphaolefin oils and/or polyester oils, may be used.
• the oil of lubricating viscosity has a kinematic viscosity at 100 °C by ASTM D445 of 1.5 to 7.5, or 2 to 7, or 2.5 to 6.5, or 3 to 6 mm 2 /s.
• the oil of lubricating viscosity comprises a poly alpha olefin having a kinematic viscosity at 100 °C by ASTM D445 of 1.5 to 7.5 or any of the other aforementioned ranges.
• Dimercaptodithiadiazole can be derivatized by the reaction product resulting from the Michael addition of a,P-unsaturated carbonyl compounds and DMTD, that is, a 1,4 addition between DMTD and a carbonyl compound, such as ester, amide, or imide groups, capable of 1,4 addition.
• the reaction products to prepare the derivatives often result in a mixture of products, the products can be provided as pure compounds as well.
• the DMTD derivatives can be represented in the pure form by Formula I:
• X is a metal, and amine, or H; where “Y” is a group derived from a carboxylate, such as an itaconate, maleate, fumarate, or a (meth)acrylate; and n is 1, 2, 3 or 4.
• Metals can include transition metals such as zinc, titanium, cobalt, zirconium, manganese, or molybdenum, for example, post-transition metals and even some metalloids, such as, for example, aluminum, antimony or boron. Where a salt is desired, it can be obtained by 1,4 addition to the ester monomer followed by reaction with a metal oxide, hydroxide or alkoxide. In some embodiments, the DMTD can be substantially free of or free of antimony.
• the carbonyl compound is a carboxylate group capable of 1,4 addition.
• carboxylate groups capable of 1,4 addition i.e., a,P-unsatu- rated carbonyl compounds
• carboxylate groups capable of 1,4 addition can be readily envisaged by those of skill in the art, and include, both mono-carboxylates and di -carboxylates as well as higher carboxylates, e.g., tri carboxylates, tetracarboxylates, etc.
• the carboxylate may be C4 to C24 carboxylate, or C5 to C22 carboxylate, or C6 to C20 carboxylate, or even C6 to Cl 8 carboxylate.
• Example carboxylates can include, but not be limited to itaconates, citraconates, maleates, fumarates, mesaconates, as well as (meth)acrylates (where the parentheses “()” around (meth) indicate the methyl group may or may not be present).
• the carboxylates herein are in the form of an ester.
• the carbonyl compound may be in the form of an amide or imide.
• group for example as in a (meth)acrylate group, depending on the context, refers to the structure of the stated group on its own or as the structure in which the group would form after reaction with another compound.
• An example of the DMTD derivative can include the DMTD derivative resulting from the 1,4 addition between DMTD and a methacrylate, for example wherein the substituent Y of the DMTD derivatives of Formula I can be, for example, a methyl methacrylate group, for example, as represented by Formula IE Formula II
• the DMTD derivative could also be salted, for example, by reacting Formula II with a half a molar equivalent of a metal oxide, hydroxide or alkoxide, such as a zinc oxide to form a compound represented, for example, by Formula Ila:
• a further example can include the DMTD derivative resulting from the 1,4 addition between DMTD and an acrylate, wherein the substituent Y of the DMTD derivatives of Formula I can be, for example, a 2-ethylhexyl acrylate group, for example, as represented by Formula III:
• a salt of the foregoing formula can be prepared by the reaction with a metal hydroxide, such as, for example, a titanium alkoxide to obtain the salt of Formula Illa below.
• a metal hydroxide such as, for example, a titanium alkoxide
• a still further example can include the DMTD derivative resulting from the 1,4 addition between DMTD and a maleate, wherein the substituent Y of the DMTD derivatives of Formula I can be, for example, a di ethylhexyl maleate group, for example, as represented by Formula IV:
• DMTD derivatives resulting from the 1,4 addition between DMTD and a dialkyl itaconate such as dimethyl itaconate, dimethyl citraconate, dimethyl fumarate, and dimethyl mesaconate and the like.
• DMTD derivatives resulting from the Michael addition of an a,P-unsaturated carbonyl compounds and DMTD, salted with an amine compound.
• the amine compounds may include tetra methyl ethylene diamine or tolytriazole.
• Other examples of amines which may be suitable as the amine salt include mono-, di-, or tri -substituted amine with secondary and tertiary amines preferred.
• alkylamines such as methylamine, ethylamine, n-propylamine, n-butylamine, n-hexylamine, n-octylamine, 2-ethylhexyla- mine, benzylamine, 2-phenylethylamine, cocoamine, oleylamine, and tridecylamine (CAS #86089-17-0); secondary and tertiary alkylamines such as isopropylamine, sec- butylamine, t-butylamine, tert-hexylamine, 1 -methyl- 1 -amino-cyclohexane, tert-octyl- amine, tert-decylamine, tert-dodecylamine, tert-tetradecylamine, tert-hexadecylamine, tertoctadecylamine, tert-tetrac
• the DMTD derivatives can be employed in an automotive or industrial lubricant at 0.05 wt.% to 2 wt.%, or from 0.08 wt.% to 1.8 wt.%, or even from 0.1 wt.% to 1.6 wt.% or 0.12 wt.% to 1.4 wt.% or even 0.15 wt.% to 1.2 or even 0.2 to 1 wt.%, or even, or even 0.3 to 1 wt.% or 0.35 to 1 wt.%, or even 0.4 to 1 wt.%.
• the DMTD derivative can be present in an amount to deliver at least 0.05% to 0.35% by weight or 0.07% to 0.3% by weight or 0.08% to 0.26% by weight sulfur to the lubricating composition.
• the sulfurized olefins employed in the present technology encompass mixtures, the compositions of which are not easily described aside from the reaction used to prepare them.
• the sulfurized olefins are about 80% polysulfides, mostly di-t- butyl polysulfides, with a range of sulfur atoms of between 3 and 8.
• the mixtures may be generically represented by the formula: RI-SX-R.2, where Ri and R2 separately are derived from 2 to 6 carbon atom containing olefins and x is an integer of between 1 and 10, with the proviso that the sulfurized olefin will have a sulfur content of from about 10 to about 50 wt%.
• the sulfurized olefins are the reaction products of olefins containing from two to six carbon atoms reacted with hydrogen sulfide and sulfur under super-atmospheric pressure in the presence of a catalyst.
• Olefinic compounds which may be sulfurized by the method of this invention are diverse in nature and may be substituted or un-substituted. The nature of the substituents if/when the olefin is substituted is not normally a critical aspect of the technology and any such substituent is useful so long as it is or can be made compatible with lubricating environments and does not interfere under the contemplated reaction conditions.
• substituted compounds which are so unstable as to deleteriously decompose under the reaction conditions employed are not contemplated.
• substituents such as keto or aldehyde can desirably undergo sulfurization.
• suitable substituents are within the skill of the art or may be established through routine testing.
• Typical of such substituents include any of the above-listed moi eties as well as hydroxy, amidine, amino, sulfonyl, sulfinyl, sulfonate, nitro, phosphate, phosphite, alkali metal mercapto and the like.
• Example olefins from which the sulfurized olefin can be prepared can contain from 2 to 30 carbon atoms. In some cases the olefins can contain two to 16 carbon atoms. Often, the olefins can contain two to six carbon atoms.
• the sulfurized olefin may also be prepared from an olefin containing from three to five carbon atoms.
• the olefin can be butylene.
• the olefin can also be isobutylene.
• Amylene may also be employed as the olefin.
• the olefin may also be isoamylene.
• the olefin may also be diisobutylene.
• Sulfurized olefins suitable for use herein may be prepared from mixtures of any of the foregoing olefins.
• the amounts of sulfur and hydrogen sulfide per mole of olefinic compound are, respectively, about 0.3-2.0 gram-atoms and about 0.1-1.5 moles.
• the preferred ranges are about 0.5- 1.5 gram-atoms and about 0.4-1.25 moles respectively, and the most desirable ranges are about 0.7-1.2 gram-atoms and about 0.4-0.8 mole respectively.
• the temperature range in which the sulfurization reaction is carried out is generally about 50°-350° C.
• the preferred range is about 100°-200° C, with about 125°- 180° C being especially suitable.
• the reaction is conducted under superatmospheric pressure; this may be and usually is autogenous pressure (i.e., the pressure which naturally develops during the course of the reaction) but may also be externally applied pressure.
• the exact pressure developed during the reaction is dependent upon such factors as the design and operation of the system, the reaction temperature, and the vapor pressure of the reactants and products and it may vary during the course of the reaction.
• materials useful as sulfurization catalysts may be acidic, basic or neutral.
• Useful neutral and acidic materials include acidified clays such as "Super Filtrol", p-toluenesul- fonic acid, dialkyl-phosphorodithioic acids, and phosphorus sulfides such as phosphorus pentasulfide.
• the preferred catalysts are basic materials. These may be inorganic oxides and salts such as sodium hydroxide, calcium oxide and sodium sulfide. The most desirable basic catalysts, however, are nitrogen bases including ammonia and amines.
• the amines includes primary, secondary and tertiary hydrocarbyl amines wherein the hydro- carbyl radicals are alkyl, aryl, aralkyl, alkaryl or the like and contain about 1-20 carbon atoms.
• Suitable amines include aniline, benzylamine, dibenzylamine, dodecylamine, naphthylamine, tallow amines, N-ethyldipropylamine, N-phenylbenzylamine, N,N-di- ethylbutyl amine, m-toluidine and 2,3-xylidine. Also useful are heterocyclic amines such as pyrrolidine, N-methylpyrrolidine, piperidine, pyridine and quinoline.
• the preferred basic catalysts include ammonia and primary, secondary, or tertiary alkylamines having about 1-8 carbon atoms in the alkyl radicals.
• Representative amines of this type are methylamine, dimethylamine, trimethylamine, ethylamine, diethylamine, triethylamine, di-n-butylamine, tri-n-butylamine, tri-sec-hexylamine and tri-n-octylamine. Mixtures of these amines can be used, as well as mixtures of ammonia and amines.
• the amount of catalytic material used is generally about 0.05-2.0% of the weight of the olefinic compound.
• the preferred ammonia and amine catalysts about 0.0005-0.5 mole per mole of olefin is preferred, and about 0.001-0.1 mole is especially desirable.
• the sulfurized olefins can also include oligomeric polysulfides of C4Sx(C4S y )bC4, where b can be 0 to 8, and x and y can be 1 to 3, such as those prepared by the processes taught, for example, in U.S. Patent Nos. 2,708,199 and 3,697,499.
• the oligomeric polysulfide can contain from 30 to 60 wt.%, or in some embodiments, from 35 to 55 wt.%, or even from 40 to 50 wt.% sulfur.
• such oligomeric polysulfides are prepared by forming an adduct between 1 to 2 moles of olefin and a sulfur halide, followed by reacting the adduct with an alkali metal sulfide, optionally in the presence of free sulfur.
• the amount of sulfurized olefin in the automotive or industrial gear oil may be 0.01 to 10 percent by weight.
• Alternative amounts of the sulfurized olefin may be 0.1 to 8 percent, or 0.2 to 6 percent, or 0.5 to 5 percent by weight, or 2 to 5% by weight sulfurized olefin or 3.5 to 5% by weight sulfurized olefin.
• the amount of sulfurized olefin present may be suitable to provide sulfur to the lubricant formulation in an amount of 0.5 to 3 wt% sulfur, or 1.5 to 2.5 wt% sulfur, or 0.5 to 1 wt% sulfur.
• the amount may also be suitable to provide the lubricant formulation from 0.75 to 2.75 wt% sulfur.
• the amount may also be suitable to provide the lubricant formulation from 1 to 2.5 wt% sulfur.
• sulfurized olefin will typically comprise a mixture of various individual chemical species.
• Reference herein to a sulfurized olefin will be understood by those of ordinary skill to encompass mixtures of such compounds as may be prepared by the described syntheses.
• the amine alkyl(thio)phosphate can include an amine phosphate, that is, a phosphate that is substantially sulfur-free.
• substantially sulfur free it is meant that sulfur is not intentionally added to the amine phosphate, and preferably the amine phosphate is completely free of sulfur.
• sulfur contamination levels may be less than 2.5%, or 1%, 0.1%, or 0.01% by weight to be considered substantially sulfur free.
• the amine phosphate may include at least 30 mole percent of the phosphorus atoms in an alkyl pyrophosphate structure, as opposed to an orthophosphate (or monomeric phosphate) structure.
• the percentage of phosphorus atoms in the pyrophosphate structure may be 30 to 100 mole %, or 40 to 90 % or 50 to 80% or 55 to 70 % or 55 to 65%.
• the remaining amount of the phosphorus atoms may be in an orthophosphate structure or may consist, in part, in unreacted phosphorus acid or other phosphorus species.
• up to 60 or up to 50 mole percent of the phosphorus atoms are in mono- or di-alkyl-orthophosphate salt structure.
• the extent of neutralization of the amine phosphate in practice may be 50% to 100%, or 80% to 99%, or 90% to 98%, or 93% to 97%, or about 95%.
• the amine phosphate may also include some amount of partial esters including mono- and diesters of the orthophosphate structure and diesters of the pyrophosphate structure.
• the alkyl groups of the amine phosphate may independently be primary or secondary groups, or a mixture of both primary and secondary. In certain embodiments at least 80 mole percent, or at least 85, 90, 95, or 99 percent, of the alkyl groups will be secondary alkyl groups. In certain embodiments at least 25 mole percent, or at least 30, 40, 50, 60, 70, 80 or 90 or even 99 mole percent, of the alkyl groups will be primary alkyl groups.
• the alkyl groups will have 3 or 4 to 12 carbon atoms, or 3 to 8, or 4 to 6, or 5 to 10, or 6 to 8 carbon atoms.
• the alkyl groups can be straight chain, branched, cyclic or aromatic.
• Such groups include 2-butyl, 2-pentyl, 3 -pentyl, 3-methyl- 2 -butyl, 2-hexyl, 3 -hexyl, cyclohexyl, 4-methyl-2-pentyl, and other such secondary groups and isomers thereof having 6, 7, 8, 9, 10, 11, or 12 carbon atoms as well as propyl, butyl, isobutyl, pentyl, 3 -methylbutyl, 2-methylbutyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, phenethyl, and other such primary groups and isomers thereof having 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 carbon atoms.
• the alkyl group will have a methyl branch at the a-position of the group, an example being the 4-methyl-2- pentyl (also referred to as 4-methylpent-2-yl) group.
• Such amine alkyl(thio)phosphates are known, for example, from W02017/079016.
• the amine alkyl(thio)phosphate may also be an amine alkylthiophosphate, wherein the alkylthiophosphate is represented by the formula (R’O)2PSSH, wherein each R’ is independently a hydrocarbyl group containing from about 3 to about 30, preferably from about 3 up to about 18, or from about 3 up to about 12, or from up to about 8 carbon atoms.
• Example R’ groups can include isopropyl, isobutyl, n-butyl, sec-butyl, the various amyl, n-hexyl, methylisobutyl carbinyl, heptyl, 2-ethylhexyl, isooctyl, nonyl, behenyl, decyl, dodecyl, and tridecyl groups.
• Illustrative lower alkylphenyl R’ groups include butylphenyl, amylphenyl, heptylphenyl, etc.
• mixtures of R’ groups include: 1-butyl and 1-octyl; 1-pentyl and 2-ethyl-l -hexyl; isobutyl and n- hexyl; isobutyl and isoamyl; 2-propyl and 2-methyl-4-pentyl; isopropyl and sec-butyl; and isopropyl and isooctyl.
• the alkylthiophosphate of the amine alkylthiophosphate may be reacted with an epoxide or a polyhydric alcohol, such as glycerol.
• This reaction product may be used alone, or further reacted with a phosphorus acid, anhydride, or lower ester.
• the epoxide is generally an aliphatic epoxide or a styrene oxide. Examples of useful epoxides include ethylene oxide, propylene oxide, butene oxide, octene oxide, dodecene oxide, styrene oxide, etc. Ethylene oxide and propylene oxide are preferred.
• the glycols may be aliphatic glycols having from 2 to about 12, or from about 2 to about 6, or from 2 or 3 carbon atoms.
• Glycols include ethylene glycol, propylene glycol, and the like.
• the alkylthiophosphate, glycols, epoxides, inorganic phosphorus reagents and methods of reacting the same are described in U.S. Pat. Nos. 3,197,405 and 3,544,465 which are incorporated herein by reference for their disclosure to these.
• Amine Component - The amine component of the amine alkyl(thio)phosphate may be represented by R 2 3NH, where each R 2 is independently hydrogen or a hydrocarbyl group or an ester-containing group, or an ether-containing group, provided that at least one R 2 group is a hydrocarbyl group or an ester-containing group or an ether-containing group (that is, not NEE).
• Suitable hydrocarbyl amines include primary amines having 1 to 18 carbon atoms, or 3 to 12, or 4 to 10 carbon atoms, such as methylamine, ethylamine, propylamine, isopropylamine, butylamine and isomers thereof, pentylamine and isomers thereof, hexylamine and isomers thereof, heptylamine and isomers thereof, octylamine and isomers thereof such as isooctylamine and 2-ethylhexylamine, as well as higher amines.
• Other primary amines include dodecylamine, fatty amines as n-octylamine, n- decylamine, n-dodecylamine, n-tetradecylamine, n-hexadecylamine, n-octadecylamine, 2-ethylhexylamine, 2-propylhexylamine and oleylamine.
• fatty amines include commercially available fatty amines such as “Armeen®” amines (products available from Akzo Chemicals, Chicago, Ill.), such as Armeen® C, Armeen® O, Armeen® OL, Armeen® T, Armeen® HT, Armeen® S and Armeen® SD, wherein the letter designation relates to the fatty group, such as coco, oleyl, tallow, or stearyl groups.
• Secondary amines that may be used include dimethylamine, diethylamine, dipropylamine, dibutylamine, diamylamine, dihexylamine, diheptylamine, methylethylamine, ethylbutylamine, bis-2-ethylhexylamine, N-methyl-1 -amino-cyclohexane, Armeen® 2C, and ethyl amyl amine.
• the secondary amines may be cyclic amines such as piperidine, piperazine and morpholine.
• Suitable tertiary amines include tri-n-butylamine, tri-n-octylamine, tri-decyl- amine, tri-laurylamine, tri-hexadecylamine, and dimethyloleylamine (Armeen® DMOD). Triisodecylamine or tridecylamine and isomers thereof may be used.
• tertiary alkyl primary amines include tertbutylamine, tert-hexylamine, tert-octylamine (such as 1,1 -dimethylhexylamine), tertdecylamine (such as 1,1 -dimethyloctylamine), tert-dodecylamine, tert-tetradecyl amine, tert-hexadecylamine, tert-octadecylamine, tert-tetracosanylamine, and tert- octacosanylamine.
• a useful mixture of amines includes “Primene® 81R” or “Primene® JMT.”
• Primene® 81R and Primene® JMT may be mixtures of Cl 1 to C14 tertiary alkyl primary amines and Cl 8 to C22 tertiary alkyl primary amines, respectively.
• the amine may be an ester-containing amine such as an N-hydrocarbyl-substituted y- or 6-amino(thio)ester, which is therefore a secondary amine.
• the ester-containing amine may, for example, be prepared by Michael addition of a primary amine, typically having a branched hydrocarbyl group, with an ethylenically unsaturated ester or thio ester, or, for example, by reductive amination of the esters of 5- oxy substituted carboxylic acids or 5-oxy substituted thiocarboxylic acids.
• the amine alkyl(thio)phosphate may be a phosphate amine of formulas (I) or (II), or variants thereof, with the amine being 2-ethylhexylamine.
• the amine alkyl(thio)phosphate can be an amine alkylthiophosphate that is the reaction product of a Ci4 to Cis alkylated dialkyldithiophosphoric acid with Primene 81RTM (produced and sold by Dow) which is a mixture of Cn to Ci4 tertiary alkyl primary amines.
• the amine alkyl(thio)phosphate can include combinations of amine phosphates, combinations of amine alkylthiophosphates, and combinations of amine phosphates with amine alkylthiophosphates.
• the amount of amine alkyl(thio)phosphate in the automotive or industrial gear oil may be 0.01 to 5 percent by weight.
• Alternative amounts of the amine alkyl(thio)phos- phate may be 0.2 to 3 percent, or 0.6 to 2 percent, or even 0.7 to 1.75 percent, or 0.2 to 1.2 percent, or 0.5 to 2.0 percent, or 0.55 to 1.4 percent, or 0.6 to 1.3 percent, or 0.7 to 1.2, or 1 to 2, or even 1.5 to 2, or 1.2 to 1.8 percent by weight or even from 1.8 to 2.2 percent by weight.
• the amount may be suitable to provide phosphorus to the lubricant formulation in an amount of 200 to 3000 parts per million by weight (ppm), or 400 to 2000 ppm, or 300 to 2000, or 600 to 1500 ppm, or 700 to 1100 ppm, or 900 to 1900, or 1100 to 1800 ppm, or 1200 to 1600 ppm or 1500 to 2000 ppm.
• ppm parts per million by weight
• amine alkyl(thio)phosphate will typically comprise a mixture of various individual chemical species.
• Reference herein to an amine alkyl(thio)phosphate will be understood by those of ordinary skill to encompass mixtures of such compounds as may be prepared by the described syntheses.
• the automotive or industrial gear oil can also contain hydrocarbylthio-substi- tuted thiadiazoles and thiadiazole adducts such as post treated dispersants.
• hydrocarbylthio-substituted thiadiazole examples include a hydrocarbylthio-substituted 2,5-di- mercapto-l,3,4-thiadiazole, or oligomers thereof.
• the hydrocarbylthio-substituted thiadiazoles can be included at concentrations of from about 0.01 to about 2 wt%, or about 0.05 to about 1.5 wt%, or even 0.1 to about 1 wt%.
• Other materials may be present in the automotive or industrial gear oil in their conventional amounts including, for example, viscosity modifiers, dispersants, pour point additives, extreme pressure agents, antifoams, copper anticorrosion agents (such as dimercaptothiadiazole compounds), iron anticorrosion agents, friction modifiers, dyes, fragrances, optional detergents and antioxidants, and color stabilizers, for example.
• An automotive or industrial gear oil refers to an automotive or industrial gear oil having sufficient levels of additive to lubricate an industrial gear or driveline power transmitting device, including an automotive gear, such as a gear, bearing or axle, or a transmission.
• an automotive or industrial gear oil can be distinguished from other lubricants, such as engine oil lubricants, based on levels of sulfur and phosphorus.
• the automotive or industrial gear oil can have a total sulfur level of about 0.75 to about 5 wt.% based on the weight of the automotive or industrial gear oil.
• the total sulfur level can be from about 0.8 to about 4 wt.%, or even about 0.9 to about 3.5 wt.% or about 1 to about 3 wt.%.
• the automotive or industrial gear oil can have a total sulfur level of about 0.75 to about 2.7 wt.%, or even about 1 to about 2.5 wt.%, or even about 1.2 to about 2.5 wt.%, or about 1.5 to about 2.4 wt.%.
• the phosphorus can be brought to the automotive or industrial gear oil, for example, from the amine alkyl(thio)phosphate discussed above, or other phosphorus containing compounds.
• Such other phosphorus containing compounds can include, for example, phosphites or phosphonates. Suitable phosphites or phosphonates include those having at least one hydrocarbyl group with 3 or 4 or more, or 8 or more, or 12 or more, carbon atoms.
• the phosphite may be a mono-hydrocarbyl substituted phosphite, a di-hydrocarbyl substituted phosphite, or a tri-hydrocarbyl substituted phosphite.
• the phosphonate may be a mono-hydrocarbyl substituted phosphonate, a di -hydrocarbyl substituted phosphonate, or a tri-hydrocarbyl substituted phosphonate.
• the phosphite is sulphur-free i.e., the phosphite is not a thiophosphite.
• the phosphite or phosphonate may be represented by the formulae: wherein at least one R may be a hydrocarbyl group containing at least 3 carbon atoms and the other R groups may be hydrogen. In one embodiment, two of the R groups are hydrocarbyl groups, and the third is hydrogen. In one embodiment every R group is a hydrocarbyl group, i.e., the phosphite is a tri-hydrocarbyl substituted phosphite.
• the hydrocarbyl groups may be alkyl, cycloalkyl, aryl, acyclic or mixtures thereof.
• R groups in formula XII is an H group
• the compound would generally be considered a phosphite, but such a compound can often exist in between the tautomers of formula XI and XII, and thus, could also be referred to as a phosphonate or phosphite ester.
• the term phosphite as used herein, will be considered to encompass both phosphites and phospho- nates.
• the other phosphorus-containing compound can be a C3- 8 hydrocarbyl phosphite, or mixtures thereof, i.e., wherein each R may independently be hydrogen or a hydrocarbyl group having 3 to 8, or 4 to 6 carbon atoms, typically 4 carbon atoms.
• the C3-8 hydrocarbyl phosphite comprises dibutyl phosphite.
• the phosphorus-containing compound can be a C12-22 hydrocarbyl phosphite, or mixtures thereof, i.e., wherein each R may independently be hydrogen or a hydrocarbyl group having 12 to 24, or 14 to 20 carbon atoms, typically 16 to 18 carbon atoms.
• the C12-22 hydrocarbyl phosphite comprises a C16-18 hydrocarbyl phosphite.
• alkyl groups for R 3 , R 4 and R 5 include octyl, 2- ethylhexyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, octadecenyl, nonadecyl, eicosyl or mixtures thereof.
• the C 12-22 hydrocarbyl phosphite may be present in the automotive or industrial gear oil at about 0.05 wt.% to about 4.0 wt.% of the automotive or industrial gear oil, or from about 0.05 wt.% to about 3 wt.%, or from about 0.05 wt.% to about 1.5 wt.%, or from about 0.05 wt.% to about 1 wt.%, or from about 0.1 wt.% to about 0.5 wt.% of the automotive or industrial gear oil.
• the other phosphorus containing compound can include both a C3-8 and a C12 to C24 hydrocarbyl phosphite.
• the phosphite ester comprises the reaction product of (a) a monomeric phosphoric acid or an ester thereof with (b) at least two alkylene diols; a first alkylene diol (i) having two hydroxy groups in a 1,4 or 1,5 or 1,6 relationship; and a second alkylene diol(ii) being an alkyl-substitute 1,3-propylene glycol.
• Sulfur containing phosphites can include, for example, a material represented by the formula [R 1 O(OR 2 )(S)PSC2H4(C)(O)OR 4 O]nP(OR 5 )2-n(O)H, wherein R 1 and R 2 are each independently hydrocarbyl groups of 3 to 12 carbon atoms, or 6 to 8 carbon atoms, or wherein R 1 and R 2 together with the adjacent O and P atoms form a ring containing 2 to 6 carbon atoms; R 4 is an alkylene group of 2 to 6 carbon atoms or 2 to 4 carbon atoms; R 5 is hydrogen or a hydrocarbyl group of 1 to about 12 carbon atoms; and n is 1 or 2.
• the C12-22 hydrocarbyl phosphite may be present in the automotive or industrial gear oil at about 0.05 wt.% to about 1.5 wt.% of the automotive or industrial gear oil, or from about 0.1 wt.% to about 1.0 wt.% of the automotive or industrial gear oil.
• the other phosphorus containing compound can be a phosphorus containing amide.
• Phosphorus containing amides can be prepared by reaction of dithiophosphoric acid with an unsaturated amide.
• unsaturated amides include acrylamide, N,N’ -methylene bisacrylamide, methacrylamide, crotonamide and the like.
• the reaction product of the phosphorus acid and the unsaturated amide may be further reacted with a linking or a coupling compound, such as formaldehyde or paraformaldehyde.
• the phosphorus containing amides are known in the art and are disclosed in U.S. Pat. Nos. 4,670,169, 4,770,807 and 4,876,374 which are incorporated by reference for their disclosures of phosphorus amides and their preparation.
• the automotive or industrial gear oil can also have a total phosphorus level of about 0.01 to about 0.5 wt.%, or 0.03 to about 0.35 wt.%, or even about 0.05 to about 0.3 wt.%, or even about 0.1 to about 0.2 or about 0.12 to about 0.17.
• the automotive or industrial gear oil can also include a rust inhibitor.
• Rust inhibitors include organic compounds having one or more of an amine group, an ether group, a hydroxyl group, a carboxylic acid, ester, or salt group, or a nitrogen-containing heterocyclic group.
• Examples include fatty amines such as oleylamine, hydroxyamines such as isopropanolamine; condensates of hydroxyamines with fatty acids (such as the product of tall oil fatty acid with diethanolamine or with N- hydroxyethylethylenediamine), carboxylic acids, esters, and salts (such as alkyl substituted succinic acids, esters, and amine or ammonium salts, e.g., the mono- or diester from a succinic acid and propylene oxide), and compounds with multiple functionalities. Examples of the latter include sarcosine derivatives, having amide and acid functionality (e.g., R'CO— NR. 2 — CH2— COOH).
• Materials with nitrogen-containing heterocyles include triazole compounds such as tolyltriazole and triazine salts.
• Other rust inhibitors include ethoxylated phenols.
• Other rust inhibitors include various oxygenated materials that may be formed by partial oxidation of waxes or oils. Examples include paraffinic oil oxidates, wax oxidates, and petroleum oxidates.
• Other rust inhibitors include organic boron compounds such as long chain alkenyl amide borates.
• alkali metal sulfonates such as sodium sulfonates and sodium alkylbenzenesulfonates.
• esters of hydroxy-acids such as tartaric acid, citric acid, malic acid, lactic acid, oxalic acid, glycolic acid, hydroxypropionic acid, and hydroxy glutaric acid.
• esters including tartrate esters (that is, especially the diesters), formed from C6-12 or Ce-io or Cs-io alcohols, e.g., isotridecyl tartrate, 2-ethylhexyl tartrate, and mixed tartrate esters of C12-14 linear alcohol/Cn branched alcohol (e.g., 80-95:20-5 ratios or 90: 10 ratio). Amides and imides of such materials may also be useful.
• rust inhibitors include polyethers. These include polyalkylene oxides such as polyethylene oxide, polypropylene oxide, and copolymers of ethylene oxide and propylene oxide. Such polyethers may be capped at one end with an alkyl group such as a butyl group. Materials of this type are commercially available and are believed to be butyl-capped polypropylene oxides or butyl-capped ethylene oxidepropylene oxide copolymers. Such materials, if they contain a hydroxy group at one end of the chain, may also be referred to as polyether alcohols or polyether polyols.
• the rust inhibitor can be a polyether.
• the rust inhibitor can be one or more of a fatty amine, a condensate of a hydroxyamine with a fatty acid, a carboxylic acid, ester, or salt, a sarcosine derivative, a triazole compound, an ethyoxylated phenol, a partially oxidized wax or oil, a long chain alkenyl amide borate, an ester of a hydroxy acid, or a sodium sulfonate.
• the rust inhibitor can be present from 0.02 to 2 percent by weight of the automotive or industrial gear oil and in alternative embodiments 0.05 to lwt% or 0.1 to 0.5wt% or 0.1 to 0.2wt%.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 2 and 25 cSt.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 2 and 15 cSt.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 2 and 12 cSt.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 2 and 9 cSt.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 2 and 7 cSt.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 2 and 6 cSt.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 2 and 5 cSt.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 3 and 6.5 cSt.
• the automotive or industrial gear oil may have a kinematic viscosity at 100 °C by ASTM D445 of between 3 and 5.5 cSt.
• the disclosed technology in general provides a method of reducing power loss and reducing operating temperature in an automotive or industrial gear by providing to an automotive or industrial gear the automotive or industrial gear oil, and operating the automotive or industrial gear.
• the technology also provides a method of improving the operating efficiency of a gear, by lubricating the gear with the automotive or industrial gear oil and operating the gear.
• the technology provides a method of improving the operating efficiency of a new gear, by lubricating the gear with the automotive or industrial gear oil and operating the gear.
• new gear it means a gear that has not been previously used in operation. Efficiency may also be improved in a used gear that was previously operated under a fluid outside the composition taught herein.
• the disclosed technology provides a method of lubricating a driveline power transmitting device, comprising supplying thereto an automotive or industrial gear oil as described herein, that is, an automotive or industrial gear oil containing (a) an oil of lubricating viscosity, (b) a DMTD derivative as discussed herein and optional other additives, such as, for example, sulfurized olefin or in some instance, (a) an oil of lubricating viscosity, (b) a DMTD derivative as discussed herein and optional other additives, such as, for example, sulfurized olefin, and amine alkyl(thio)phosphate, and operating the driveline power transmitting device for a sufficient period to allow the automotive or industrial gear oil to minimize power losses and reduce operating temperatures of the driveline power transmitting device in a controlled manner to a greater extent than a typical gear lubricant.
• This reduction in power loss can be measured during operation of the device with the automotive or industrial gear oil.
• the driveline power transmitting device may comprise at least two gears as in a gearbox of a vehicle (e.g., a manual transmission) or in an axle or differential, or in other driveline power transmitting devices.
• the driveline power transmitting device may also include bearings.
• the rolling elements of the bearings may be cylindrical or ball in design.
• Lubricated gears of a differential may include amboid, or spiral bevel, or more commonly hypoid gears, such as those for example in a drive axle.
• the axles may have a gear ratio of 2: 1 to 8: 1, and the ring gear maybe be approximately 13 to 64 cm in diameter.
• the axle may incorporate an open differential or some type of traction enabling device.
• the axle may be part of a drivetrain with one or more drive axles, such as a tandem or tridem design, in which the axles may be coupled together with a power divider.
• Application of these axles includes light, medium and heavy duty vehicles (e.g. vocational or line haul service), and could be used on or off highway.
• the axle may be from a traditional petroleum powered vehicle, may be from an electrically driven vehicle, or a hybrid thereof.
• the electrically driven axle can combine an electric motor, power electronics and transmission in a unit directly powering the vehicle's axle, where the electronics of the electric motor, power electronics, etc. are protected from the automotive or industrial gear oil.
• the lubricant should be able to meet the other aspects expected of it in normal operation of the driveline power transmitting device.
• condensation product is intended to encompass esters, amides, imides and other such materials that may be prepared by a condensation reaction of an acid or a reactive equivalent of an acid (e.g., an acid halide, anhydride, or ester) with an alcohol or amine, irrespective of whether a condensation reaction is actually performed to lead directly to the product.
• an acid e.g., an acid halide, anhydride, or ester
• a particular ester may be prepared by a transesterification reaction rather than directly by a condensation reaction.
• the resulting product is still considered a condensation product.
• each chemical component described is presented exclusive of any solvent or diluent oil, which may be customarily present in the commercial material, that is, on an active chemical basis, unless otherwise indicated.
• each chemical or composition referred to herein should be interpreted as being a commercial grade material which may contain the isomers, by-products, derivatives, and other such materials which are normally understood to be present in the commercial grade.
• hydrocarbyl substituent or “hydrocarbyl group” is used in its ordinary sense, which is well-known to those skilled in the art. Specifically, it refers to a group having a carbon atom directly attached to the remainder of the molecule and having predominantly hydrocarbon character.
• hydrocarbyl groups include:
• hydrocarbon substituents that is, aliphatic (e.g., alkyl or alkenyl), alicyclic (e.g., cycloalkyl, cycloalkenyl) substituents, and aromatic-, aliphatic-, and alicyclic-substituted aromatic substituents, as well as cyclic substituents wherein the ring is completed through another portion of the molecule (e.g., two substituents together form a ring);
• aliphatic e.g., alkyl or alkenyl
• alicyclic e.g., cycloalkyl, cycloalkenyl
• aromatic-, aliphatic-, and alicyclic-substituted aromatic substituents as well as cyclic substituents wherein the ring is completed through another portion of the molecule (e.g., two substituents together form a ring);
• substituted hydrocarbon substituents that is, substituents containing nonhydrocarbon groups which, in the context of this invention, do not alter the predominantly hydrocarbon nature of the substituent (e.g., halo (especially chloro and fluoro), hydroxy, alkoxy, mercapto, alkylmercapto, nitro, nitroso, and sulfoxy); • hetero substituents, that is, substituents which, while having a predominantly hydrocarbon character, in the context of this invention, contain other than carbon in a ring or chain otherwise composed of carbon atoms and encompass substituents as pyridyl, furyl, thienyl and imidazolyl. Heteroatoms include sulfur, oxygen, and nitrogen. In general, no more than two, or no more than one, non-hydrocarbon substituent will be present for every ten carbon atoms in the hydrocarbyl group; alternatively, there may be no non-hydrocarbon substituents in the hydrocarbyl group.
• Dimercaptothiadiazole (DMTD; 100.2g) and ethylacetate (solvent; 200ml) were added to a reaction vessel and stirred to form a slurry.
• the mixture was heated to 25 °C and 2-ethylhexyl acrylate (122.6g) was added dropwise over 40 minutes.
• the reaction mixture was heated to 45 °C and held for 2.5 hours.
• Ethylacetate was removed under vacuum at 60 °C, and the desired product was obtained after filtration through diatomaceous earth. A yellow oil was obtained as the product.
• axles used were obtained from a North American tier I supplier. Each efficiency test was run with a new axle and no temperature control. The temperature was allowed to self-stabilize over time.
• Table 3 is a speed-load map that represents 16 sets of conditions that includes 4 different pinion speeds and 5 different pinion loads.
• stage 16 The test runs sequentially through each stage 1-16. One cycle is completed after the fluid has been subjected once to all 16 stages. The test is repeated for 10 cycles. The power loss and fluid temperature are measured after each stage and recorded. The power loss and temperature data reported here are for stage 16 of the procedure. Stage 16 exposes the fluid to the both the highest speed and highest load conditions. As it is the highest power stage, it shows the difference in power loss and operating temperature more dramatically than other stages. Data from cycle 1, cycle 3 and cycle 10 is reported for each fluid. Minimization of both power loss and operating temperature is most desirable.
• Each sample contains 4wt% sulfurized olefin as the EP/antiwear agent.
• Sample 1 contains no additional co-EP agent.
• Sample 2 and Sample 3 contain oil soluble derivatives of dimercaptothiadiazole where the effective concentration of dimercaptothiadizole delivered is equivalent for both samples at 0.35wt%.
• Sample 2 contains a dialkyldimercaptothiadiazole at 1.0wt% and Sample 3 contains the reaction product of dimercaptothiadiazole with 2-ethylhexyl acrylate at 0.78wt%. There is an improvement for both power loss and operating temperature observed for Sample 2 compared to Sample 1.
• Sample 4 contains a dispersant that has been post treated with dimercaptothiadiazole - as this is another method for solubilizing the dimercaptothiadiazole in oil.
• the treat rate of the dispersant is 2.5wt%. This delivers 0.13wt% dimercaptothiadiazole to the fully formulated fluid.
• the reaction product of DMTD and 2-ethylhexylacrylate was treated at 0.29wt% to give the identical effective concentration of DMTD to the post treated dispersant.
• the transitional term “comprising,” which is synonymous with “including,” “containing,” or “characterized by,” is inclusive or open-ended and does not exclude additional, un-recited elements or method steps.
• the term also encompass, as alternative embodiments, the phrases “consisting essentially of’ and “consisting of,” where “consisting of’ excludes any element or step not specified and “consisting essentially of’ permits the inclusion of additional un-recited elements or steps that do not materially affect the essential or basic and novel characteristics of the composition or method under consideration.
• the expression “consisting of’ or “consisting essentially of,” when applied to an element of a claim, is intended to restrict all species of the type represented by that element, notwithstanding the presence of “comprising” elsewhere in the claim.
• An automotive or industrial gear oil comprising a) an oil of lubricating viscosity; b) a DMTD derivative comprising the reaction product of DMTD and at least one C4 to C24 carboxylate, wherein the lubricant comprises a total sulfur level of about 0.75 to about 5 wt%.
• the automotive or industrial gear oil of any previous sentence comprising a total sulfur level of about 1 to about 2.5 wt.%.
• the automotive or industrial gear oil of any previous sentence comprising a total sulfur level of about 1.2 to about 2.5 wt.%.
• the sulfurized olefin comprises oligomeric polysulfide of C4Sx(C4S y )bC4, where b can be 0 to 8, and x and y can be 1 to 3.
• the sulfurized olefin comprises a mixture of sulfurized olefins of formula RI-SX-R.2 where Ri and R2 separately are derived from 2 to 6 carbon atom containing olefins and x is an integer of between 1 and 10, with the proviso that the sulfurized olefin will have a sulfur content of from about 10 to about 50 wt%.
• the automotive or industrial gear oil of any previous sentence further comprising 0.55 to 1.4 wt% of an amine alkyl(thio)phosphate compound.
• the automotive or industrial gear oil of any previous sentence further comprising 0.6 to 1.3 wt% of an amine alkyl(thio)phosphate compound.
• the automotive or industrial gear oil of any previous sentence further comprising amine alkyl(thio)phosphate compound suitable to provide phosphorus to the gear oil in an amount of 1100 to 1800 ppm.
• the automotive or industrial gear oil of any previous sentence further comprising amine alkyl(thio)phosphate compound suitable to provide phosphorus to the gear oil in an amount of 1200 to 1600 ppm.
• the amine phosphate comprises a substantially sulfur-free alkyl phosphate amine salt wherein at least about 30 mole percent of the phosphorus atoms are in an alkyl pyrophosphate salt structure and at least about 80 mole percent of the alkyl groups are secondary alkyl groups of about 3 to about 12 carbon atoms.
• the amine phosphate comprises a substantially sulfur-free alkyl phosphate amine salt wherein at least about 30 mole percent of the phosphorus atoms are in an alkyl pyrophosphate salt structure and at least about 25 mole percent of the alkyl groups in such a sulfur-free alkyl phosphate can be primary alkyl groups of about 3 to about 12 carbon atoms.
• a method of reducing power losses in a driveline power transmitting device comprising providing to the driveline power transmitting device the automotive or industrial gear oil of any previous sentence, and operating the driveline power transmitting device.
• a method of reducing the operating temperatures of a gear comprising lubricating the gear with the automotive or industrial gear oil as claimed in any previous sentence directed to automotive or industrial gear oils above, and operating the gear.
• a method of improving the operating efficiency of a gear comprising lubricating the gear with the automotive or industrial gear oil as claimed in any previous sentence directed to automotive or industrial gear oils above, and operating the gear.

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