WO2011017148A1 - Compositions lubrifiantes contenant un dispersant des asphaltènes - Google Patents

Compositions lubrifiantes contenant un dispersant des asphaltènes Download PDF

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Publication number
WO2011017148A1
WO2011017148A1 PCT/US2010/043490 US2010043490W WO2011017148A1 WO 2011017148 A1 WO2011017148 A1 WO 2011017148A1 US 2010043490 W US2010043490 W US 2010043490W WO 2011017148 A1 WO2011017148 A1 WO 2011017148A1
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Prior art keywords
composition
carbon atoms
group
lubricating
detergent
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PCT/US2010/043490
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English (en)
Inventor
William R. S. Barton
Stephen J. Cook
Daniel J. Saccomando
Alexandra Mayhew
Joanne L. Jones
Shaun P. Carney
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The Lubrizol Corporation
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Application filed by The Lubrizol Corporation filed Critical The Lubrizol Corporation
Priority to EP10744628A priority Critical patent/EP2462212A1/fr
Priority to CN201080044666.7A priority patent/CN102575185B/zh
Priority to KR1020127005681A priority patent/KR101811891B1/ko
Priority to SG2012007050A priority patent/SG178205A1/en
Priority to JP2012523652A priority patent/JP5823392B2/ja
Priority to CA2770160A priority patent/CA2770160A1/fr
Priority to US13/388,333 priority patent/US20120266837A1/en
Publication of WO2011017148A1 publication Critical patent/WO2011017148A1/fr

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    • 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
    • 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
    • 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
    • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04—Mixtures of base-materials and additives
    • C10M169/045—Mixtures of base-materials and additives the additives being a mixture of compounds of unknown or incompletely defined constitution and non-macromolecular compounds
    • 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
    • C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • 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
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02—Hydroxy compounds
    • C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027—Neutral 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
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/144—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups
    • 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
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28—Esters
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/221—Six-membered rings containing nitrogen and carbon only
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/223—Five-membered rings containing nitrogen and carbon only
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/223—Five-membered rings containing nitrogen and carbon only
    • C10M2215/224—Imidazoles
    • 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
    • C10M2215/28—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
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/30—Heterocyclic compounds
    • 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
    • C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/089—Overbased salts
    • 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
    • C10M2223/045—Metal containing thio derivatives
    • 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
    • C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01—Physico-chemical properties
    • 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
    • C10N2030/52—Base number [TBN]
    • 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
    • C10N2040/25—Internal-combustion engines
    • 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
    • C10N2040/25—Internal-combustion engines
    • C10N2040/252—Diesel engines

Definitions

  • the present invention relates to lubricating oil compositions and in particular to lubricating oil compositions suitable for medium or low speed diesel engines, such as marine diesel engines, including the four-stroke trunk- piston engine.
  • Lubricating oils for such engines are known and typically contain a range of additives which will perform a variety of functions.
  • contamination of these lubricating oil compositions with unburned residual fuel oil is a problem recognized in the industry. This leads to severe engine cleanliness problems in service which is sometimes referred to as "black paint" of asphal- tene deposits.
  • the problem is particularly widespread in marine diesel engines, such as 4-stroke trunk-piston engines where dirty cam boxes and crankcases are encountered, and 2-stroke cross-head engines which usually use two separate lubricating oils, one for the crankcase and one for the cylinder. It is in the crankcase of these 2-stroke engines where there is potential for these heavy deposits to occur.
  • the present invention provides a lubricating compositions, such as a marine diesel engine lubricating composition, comprising: (a) an oil of lubricating viscosity; (b) an asphaltene dispersant comprising a cyclic headgroup that contains a nitrogen atom and at least one other heteroatom; and (c) a detergent derived from an alkyl phenol.
  • a lubricating compositions such as a marine diesel engine lubricating composition, comprising: (a) an oil of lubricating viscosity; (b) an asphaltene dispersant comprising a cyclic headgroup that contains a nitrogen atom and at least one other heteroatom; and (c) a detergent derived from an alkyl phenol.
  • compositions of the present invention contain a minimum amount, such as least 1 weight percent, of the alkyl phenol detergent; further comprise (d) a salicylate detergent, wherein some maximum amount, such as 50 percent or less, of the total base number (TBN) of the overall composition is delivered from the salicylate detergent; or combinations thereof.
  • a salicylate detergent wherein some maximum amount, such as 50 percent or less, of the total base number (TBN) of the overall composition is delivered from the salicylate detergent; or combinations thereof.
  • the invention further provides methods of using such compositions in the operation of engine, particularly marine diesel engines.
  • compositions of the present invention contain an asphaltene dispersant that has a cyclic headgroup that contains a nitrogen atom and at least one other heteroatom.
  • the asphaltene dispersant contains at least one amidine headgroup, urea headgroup, guanidine headgroup, or combinations thereof.
  • the headgroup of the asphaltene dispersant contains a five-member ring, a six-member ring, or combinations thereof.
  • suitable asphaltene dispersants for use in the compositions and methods of the present invention include compounds represented by the following formulas:
  • each R 0 is a hydrocarbyl group containing a sufficient number of carbon atoms to render the compound oil-soluble. In other embodiments, R 0 is a hydrocarbyl containing 8 or more carbon atoms, or 8 to 250 carbon atoms. In some embodiments each R 1 is a hydrocarbyl group containing 1 to 6 carbon atoms, 1 to 2 carbon atoms, or 1 carbon atom. In some embodiments each R 2 is a hydrogen or a hydrocarbyl group containing 1 to 4 carbon atoms.
  • hydrocarbyl groups present in the formulas herein may contain hetero atoms, and in some embodiments hydrocarbyl groups such as R 0 may be groups such as -CH 2 (CH 2 ) m 0H or -CH 2 (CH 2 ) H1 NH 2 where m is 0 to 249, or 7 to 249, or at least 7.
  • the asphaltene dispersant of the present invention is a compound represented by any of the following formulas:
  • each R 1 is independently a hydrocarbylene group comprising 1 to 10 carbon atoms
  • each R 2 is independently hydrogen or a hydrocarbyl group comprising 1 to 50 carbon atoms
  • each R is independently a hydrocarbyl group containing 1 to 50 carbon atoms
  • R 4 is a hydrocarbyl group containing 1 to 200 carbon atoms
  • X is a hydrocarbylene group derived from an amine or a polyamine comprising 1 to 20 carbon atoms and 1 to 5 nitrogen atoms.
  • each R 1 is a hydrocarbylene group containing 1 to 6 carbon atoms, 1 to 2 carbon atoms, or 1 carbon atom. In other embodiments at least one R 1 group contains 1 carbon atom.
  • each R 2 is a hydrogen or a hydrocarbyl group containing 1 to 4 carbon atoms.
  • each R 3 is a hydrocarbyl group containing 8 or more carbon atoms, 8 to 30 carbon atoms, 12 to 24 carbon atoms, or 12 to 22 carbon atoms. In other embodiments at least one R group contains a sufficient number of carbon atoms to render the compound oil-soluble.
  • R4 is a hydrocarbyl group containing 20 to 200 carbon atoms or 50 to 150 carbon atoms.
  • X is a hydrocarbylene group derived from an amine or a polyamine comprising 2 to 10 carbon atoms, 4 to 8 carbon atoms, or 6 carbon atoms in addition to 1 to 5 nitrogen atoms, 1 to 3 nitrogen atoms, or 2 nitrogen atoms.
  • At least one R 2 group present in any of the compounds described above is a monounsaturated hydrocarbyl group.
  • the R 4 group, of formula (VI) is derived from polyisobutylene.
  • X is derived from a polyalkylene polyamine.
  • the various hydrocarbyl groups described for the formulas above may contain hetero atoms as well as cyclic groups, including cyclic groups formed by the linking of two or more hydrocarbyl groups present in the compound, forming a ring.
  • the hydrocarbyl groups of the formulas above contain an alkyl amine and/or a hydroxy group.
  • the asphaltene dis- persants of the present invention may also include compounds containing five member ring ureas, imidazolines, imidazoles, tetrazoles, tetrazolines, tetra- zolones, lactams, sultams, thioureas, triazoles, triazolines, pyridones, pyrimi- dones, or combinations thereof.
  • Still other examples of compounds that may be present in the asphaltene dispersants of the present invention include dihydropyrimidines, tetrahy- dropyrimi dines, pyrazole, imidazoline, dihydropyrimidinone, triazine, dihydro- triazine, tetrahydrotriazine, oxadiazoles, thiadiazole, dihydrooxadiazole, dihydrothiadiazole, or combinations thereof.
  • asphaltene dispersant compounds described above may be used alone or in combination with one another.
  • compositions of the present invention include a detergent derived from an alkyl phenol.
  • Suitable alkyl phenol detergents include phenate detergents, such as phenate sulfides, including calcium phenate sulfides.
  • phenate sulfides are neutral detergents, and in other embodiments the calcium phenate sulfides are overbased detergents.
  • the phenate may be a sulphur-containing phenate, a methylene-bridged phenate, or mixtures thereof. In one embodiment the phenate is sulphur-containing phenate.
  • the alkyl phenol detergent is present in the compositions of the present invention at 1 percent by weight or more in the overall composition. In other embodiments the alkyl phenol detergent is present at least 2, 3, 4, 6, 8 or 10 percent by weight in the overall composition.
  • the alkyl phenol detergent delivers at least 50 percent of the TBN of the overall composition. In other embodiments the alkyl phenol detergent delivers at least 60 percent, 70 percent, 75 percent, 90 percent or 95 percent of the TBN of the overall composition. In still other embodiments the compositions of the present invention are substantially free of other detergents such that alkyl phenol detergents deliver more than 99 percent, more than 99.5 percent, or even 100 percent of the TBN of the overall composition. In still further embodiments, the alkyl phenol detergent may provide at least 50, 60, 75, 90, 99 or even 100 percent of the TBN of all of the detergents present in the overall composition.
  • the phenate detergent may be a neutral or overbased material.
  • Over- based materials otherwise referred to as overbased or superbased salts, are generally single phase, homogeneous Newtonian systems characterised by an amount of excess metal that which would be necessary for neutralisation according to the stoichiometry of the metal and the particular acidic organic compound reacted with the metal.
  • the amount of excess metal is commonly expressed in terms of substrate to metal ratio.
  • substrate to metal ratio is the ratio of the total equivalents of the metal to the equivalents of the substrate. A more detailed description of the term metal ratio is provided in
  • the overbased alkali or alkaline earth metal phenate detergent may have a metal ratio of 0.8 or 1.0 to 10 or 3 to 9, or 4 to 8, or 5 to 7.
  • the phenate detergents may be overbased with calcium hydroxide.
  • the alkali or alkaline earth metal phenate detergent may have a total base number (TBN) of 30 or 50 to 400; or 200 to 350; or 220 to 300, and in another embodiment 255.
  • the phenate detergent has a TBN in the range of 30, 40 or 50 to 220, 205, or 190, and in another embodiment 150.
  • the phenate detergent has a TBN of 300 or more, 350 or more, or 400 or more, or from 300 or 350 to 400, and in another embodiment 395.
  • Suitable phenate detergents may be formed by reacting an alkylphenol, an alkaline earth metal base and sulfur, typically carried out in the presence of a promoter solvent to form a sulfurized metal phenate.
  • the alkylphenols useful in the present invention are of the formula R(C 6 H 4 )OH where R is a straight chain or branched chain alkyl group having from 8 to 40 carbon atoms and preferably from 10 to 30 carbons, and the moiety (C 6 H 4 ) is a benzene ring.
  • suitable alkyl groups include octyl, decyl, dodecyl, tetradecyl, and hexadecyl groups
  • the alkaline earth metal base can be a base of calcium, barium, magnesium and strontium. Preferred are calcium and magnesium.
  • the most commonly used bases are the oxides and hydroxides of the above metals such as calcium oxide, calcium hydroxide, barium oxide, barium hydroxide, magnesium oxide, and the like.
  • the promoter solvent also sometimes referred to as a mutual solvent, can be any stable organic liquid which has appreciable solubility for the alkaline earth metal base, the alkylphenol, and the sulfurized metal phenate intermediate.
  • Suitable solvents include glycols and glycol monoethers such as ethylene glycol, 1,4-butane diol, and derivatives of ethylene glycol, such as monomethyl ether, monoethyl ether, etc.
  • the solvent is one or more vicinal glycols and in another embodiment the solvent includes ethylene glycol.
  • the sulfur used in the reaction is elemental sulfur and may be used in the form of molten sulfur.
  • the phenate detergent is prepared in the presence of a co-surfactant.
  • suitable co-surfactants include low base alkylbenzene sulfonates, hydrocarbyl substituted acylating agents such as polyisobutenyl succinic anhydrides (PIBSA), and succinimide dispersants such as polyisobutenyl succinimides.
  • Suitable sulfonates include sulfonic acid salts from sulfonic acids having a molecular weight preferably of more than 400 obtained by sulfonating alkyl-benzenes derived from olefins or polymers of C2-C4 olefins of chain length C15-C80 and alkaline earth metals such as calcium, barium, magnesium etc.
  • Suitable co-surfactants include and/or may be derived from PIBSA, which may itself be derived from 300 to 5000, or 500 to 3000, or 800 to 1600 number average molecular weight polyisobuty- lene.
  • these phenate detergents may be overbased by reacting them with carbon dioxide gas in the presence of additional alkaline earth meal base, typically in the presence of a promoter solvent.
  • the phenate sulfide detergents of the composition can be represented by the formula:
  • the number of sulphur atoms y can be in the range from 1 to 8, preferably 1 to 6 and even more preferably 1 to 4;
  • R 5 can be hydrogen or hydrocar- byl groups;
  • T is hydrogen or an (S) y linkage terminating in hydrogen, an ion or a non-phenolic hydrocarbyl group;
  • w can be an integer from 0 to 4; and
  • M is hydrogen, a valence of a metal ion, an ammonium ion and mixtures thereof.
  • the metal can be monovalent, divalent, trivalent or mixtures of such metals.
  • the metal M can be an alkali metal, such as lithium, sodium, potassium or combinations thereof.
  • the metal M can be an alkaline earth metal, such as magnesium, calcium, barium or mixtures of such metals.
  • trivalent the metal M can be aluminum. In one embodiment the metal is an alkaline earth metal and in another embodiment the metal is calcium.
  • the monomeric units of structure (VII) combine in such a way with itself x number of times to form oligomers of hydrocarbyl phenol.
  • Oligomers are described as dimers, trimers, tetramers, pentamers and hexamers when x is equal to 0, 1 , 2, 3, and 4.
  • the number of oligomers represented by x can be in the range from 0 to 10, preferably 1 to 9, more preferably 1 to 8, even more even more preferably 2 to 6 and even more preferably 2 to 5.
  • an oligomer is present in significant quantities if concentrations are above 0.1 wt %, preferably above 1 wt % and even more preferably above 2 wt %.
  • an oligomer is present in trace amounts if concentrations are less than 0.1 wt %, for example, oligomers with 11 or more repeat units may be present.
  • x is 2 or higher.
  • the overall sulfur- containing phenate detergent contains less than 20 percent by weight dimeric structures.
  • each R 5 can be hydrogen or a hydrocarbyl group containing 4 to 80, 6 to 45, 8 to 30 or even 9 to 20 or 14 carbon atoms.
  • the number of R 5 substituents (w) other than hydrogen on each aromatic ring can be in the range from 0 to 4, 1 to 3 or even 1 to 2 or 1. Where two or more hydrocarbyl groups are present they may be the same or different and the minimum total number of carbon atoms present in the hydrocarbyl substituents on all the rings, to ensure oil solubility, can be 8 or 9.
  • the preferred components include 4-alkylated phenols containing alkyl groups with the number of carbon atoms between 9 and 14, for example 9, 10, 1 1, 12, 13, 14 and mixtures thereof.
  • the 4-alkylated phenols typically contain sulphur at position 2.
  • the phenate detergent represented by structure (VII) above may also be overbased using an alkaline earth metal base, such as calcium hydroxide.
  • the phenate detergent used in the present invention is an overbased sulfurized alkaline earth metal hydrocarbyl phenate, which may optionally be modified by the incorporation of at least one carboxylic acid having the formula: R-CH(R ⁇ -COOH where R is a Cio to C 24 straight chain alkyl group and R 1 is hydrogen, or an anhydride or ester thereof.
  • Such overbased phenates may be prepared by reacting: (a) a non-overbased sulfurized alkaline earth metal hydrocarbyl phenate as described above, (b) an alkaline earth metal base which may be added as a whole or in increments, (c) either a polyhydric alcohol having from 2 to 4 carbon atoms, a di- or tri- (C 2 to C 4 ) glycol, an alkylene glycol alkyl ether or a polyalkylene glycol alkyl ether, (d) a lubricating oil present as a diluent, (e) carbon dioxide added subsequent to each addition of component (b), and optionally (f) at least one carboxylic acid as defined above.
  • Component (b) may be any of the earth metal based described above and in some embodiments is calcium hydroxide.
  • Component (c) may suitably be either a dihydric alcohol, for example ethylene glycol or propylene glycol, or a trihydric alcohol, for example glyc- erol.
  • the di-or Id-(C 2 to C 4 ) glycol may suitably be either diethylene glycol or triethylene glycol.
  • the alkylene glycol alkyl ether or polyalkylene glycol alkyl ether may suitably be of the formula: R(OR ⁇ x OR 2 where R is a Ci to C 6 alkyl group, R 1 is an alkylene group, R 2 is hydrogen or Ci to C 6 alkyl and x is an integer in the range from 1 to 6.
  • Suitable examples include the monomethyl or dimethyl ethers of ethyleneglycol, diethylene glycol, triethylene glycol or tetraethylene glycol.
  • a particularly suitable solvent is methyl digol.
  • Mixtures of glycols and glycol ethers may also be employed.
  • the glycol or glycol ether is used in combination with an inorganic halide.
  • component (c) is either ethylene glycol or methyl digol, the latter in combination with ammonium chloride and acetic acid.
  • component (f), the carboxylic acid used to modify the phenate has an R group that is an unbranched alkyl group, which may contain from 10 to 24 or 18 to 24 carbon atoms.
  • suitable saturated carboxylic acids include capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid and lignoceric acid. Mixtures of acids may also be employed.
  • the acid anhydride or the ester derivatives of the acid preferably the acid anhydride.
  • the acid used is stearic acid.
  • sulphur additional to that already present by way of component (a), may be added to the reaction mixture.
  • the reaction described above may be carried out in the presence of a catalyst.
  • Suitable catalysts include hydrogen chloride, calcium chloride, ammonium chloride, aluminum chloride and zinc chloride
  • compositions of the present invention may further include a salicylate detergent.
  • Typical salicylate detergents are metal overbased salicylates having a sufficiently long hydrocarbon substituent to promote oil solubility.
  • Hydrocarbyl-substituted salicylic acids can be prepared by the reaction of the corresponding phenol by reaction of an alkali metal salt thereof with carbon dioxide.
  • the hydrocarbon substituent can be as described for the carboxylate or phenate detergents.
  • hydrocarbon-substituted salicylic acids may be represented by the formula
  • each R is an aliphatic hydrocarbyl group
  • y is independently 1 , 2, 3 or 4, with the proviso that R and y are such that the total number of carbon atoms provided by the R groups is at least 7 carbon atoms.
  • y is 1 or 2, and in one embodiment y is 1.
  • the total number of carbon atoms provided by the R groups may be 7 to 50, and in one embodiment 12 to 50, and in one embodiment 12 to 40, and in one embodiment 12 to 30, and in one embodiment 16 to 24, and in one embodiment 16 to 18, and in one embodiment 20 to 24.
  • y is 1 and R is an alkyl group containing 16 to 18 carbon atoms.
  • the metal salt is Infineum M7101 which is a product supplied by Infineum USA LP identified as a calcium salicylate dispersed in oil having a TBN of 168, a calcium content of 6.0% by weight, an a diluent oil concentration of 40% by weight.
  • the salicylate detergent delivers no more than
  • the salicylate detergent delivers no more than 40 percent, 30 percent, 25 percent, 10 percent or 5 percent of the TBN of the overall composition.
  • the compositions of the present invention are substantially free of salicylate detergents such that salicylate detergents deliver no more than 0.5 percent of the TBN of the overall composition, or even 0 percent of the of the TBN of the overall composition.
  • the salicylate is present in the compositions of the present invention at such amounts that no more than 30 percent, or 25 percent, of the TBN of the overall composition is provided by the salicylate detergent.
  • the invention further includes an oil of lubricating viscosity.
  • Suitable oils include natural and synthetic oils, oil derived from hydrocracking, hydrogenation, hydrofinishing, unrefined, refined and re-refined oils and mixtures thereof.
  • Unrefined oils are those obtained directly from a natural or synthetic source generally without (or with little) further purification treatment.
  • Refined oils are similar to the unrefined oils except they have been further treated in one or more purification steps to improve one or more properties.
  • Purification techniques include solvent extraction, secondary distillation, acid or base extraction, filtration, percolation and the like.
  • Re-refined oils are also known as reclaimed or reprocessed oils, and are obtained by processes similar to those used to obtain refined oils and often are additionally processed by techniques directed to removal of spent additives and oil breakdown products.
  • Natural oils useful in making the inventive lubricants include animal oils, vegetable oils (e.g., castor oil, lard oil), mineral lubricating oils such as liquid petroleum oils and solvent-treated or acid-treated mineral lubricating oils of the paraffinic, naphthenic or mixed paraffinic-naphthenic types and oils derived from coal or shale or mixtures thereof.
  • animal oils e.g., castor oil, lard oil
  • mineral lubricating oils such as liquid petroleum oils and solvent-treated or acid-treated mineral lubricating oils of the paraffinic, naphthenic or mixed paraffinic-naphthenic types and oils derived from coal or shale or mixtures thereof.
  • Synthetic lubricating oils are useful and include hydrocarbon oils such as polymerised and interpolymerised olefins (e.g., polybutylenes, poly- propylenes, propyleneisobutylene copolymers); poly(l-hexenes), poly(l- octenes), poly(l-decenes), and mixtures thereof; alkyl-benzenes (e.g.
  • dodecyl- benzenes tetradecylbenzenes, dinonylbenzenes, di-(2-ethylhexyl)-benzenes
  • polyphenyls e.g., biphenyls, terphenyls, alkylated polypheny Is
  • Other synthetic lubricating oils include but are not limited to liquid esters of phosphorus-containing acids (e.g., tricresyl phosphate, trioctyl phosphate, and the diethyl ester of decane phosphonic acid), and polymeric tetrahy- drofurans.
  • Synthetic oils may be produced by Fischer-Tropsch reactions and typically may be hydroisomerised Fischer-Tropsch hydrocarbons or waxes.
  • Oils of lubricating viscosity can also be defined as specified in the American Petroleum Institute (API) Base Oil Interchangeability Guidelines.
  • the five base oil groups are as follows: Group I (sulphur content >0.03 wt %, and/or ⁇ 90 wt % saturates, viscosity index 80-120); Group II (sulphur content ⁇ 0.03 wt %, and >90 wt % saturates, viscosity index 80-120); Group III (sulphur content ⁇ 0.03 wt %, and >90 wt % saturates, viscosity index >120); Group IV (all polyalphaolefins (PAOs)); and Group V (all others not included in Groups I, II, III, or IV).
  • the oil of lubricating viscosity comprises an API Group I, Group II, Group III, Group IV, Group V oil and mixtures thereof.
  • the oil of lubricating viscosity an API Group I,
  • Group IV oil and mixtures thereof More preferably the oil of lubricating viscosity an API Group I, Group II, Group III oil and mixtures thereof.
  • compositions of the present invention comprise: (a) an oil of lubricating viscosity; (b) an asphaltene dispersant comprising a cyclic headgroup that contains a nitrogen atom and at least one other heteroatom; and (c) a detergent derived from an alkyl phenol.
  • compositions of the present invention have a TBN of at least 25.
  • the amount of TBN delivered from the alkyl phenol detergent can be any of the minimum percentages described above.
  • the amount of TBN delivered from the salicylate detergent can be any of the maximum percentages described above.
  • the lubricating compositions of the present invention are marine diesel engine lubricants.
  • Component (a), the lubricating oil, may be present in the lubricating compositions of the present invention at 55 to 99.9, 60 to 98, 65 to 96, or 67 to 94 percent by weight.
  • Component (b), the asphaltene dispersant may be present in the lubricating compositions of the present invention at 0.1 to 6.0, 0.2 to 5.0, or 0.5 to 4.0, or even 1.0 to 4.0 or 3.0 percent by weight.
  • Component (c), the alkyl phenol derived detergent may be present in the lubricating compositions of the present invention at 0.5 to 30, 1 to 25, 2 to 22, or 5 to 20 percent by weight.
  • component (d) the salicylate detergent, may be present in the lubricating compositions of the present invention at greater than 0 to 10, 0.1 to 8, or 0.5 to 5 percent by weight.
  • compositions of the present invention may contain additional performance additives that are different from components (a)-(d).
  • additional additives may be present in the lubricating compositions of the present invention (either separately or combined) at 0 to 10, 0.1 to 7, 0.2 to 5, or even 1 to 5 percent by weight of the overall lubricating composition.
  • Additional performance additives may also be present in the lubricating compositions described herein, especially those additives that have been used in marine diesel cylinder lubricants.
  • known lubricant additives are metal salts of a phosphorus acid, including metal compounds represented by the formula:
  • R 6 and R 7 groups are independently hydrocarbyl groups that are typically free from acetylenic and usually also from ethylenic unsatura- tion. They are typically alkyl, cycloalkyl, aralkyl or alkaryl group and have 3 to 20, 3 to 16 or 3 to 13 carbon atoms.
  • the alcohol which reacts to provide the R 6 and R 7 groups can be a mixture of a secondary alcohol and a primary alcohol, for instance, a mixture of 2-ethylhexanol and 2-propanol or, alternatively, a mixture of secondary alcohols such as 2-propanol and 4-methyl-2-pentanol.
  • Such materials are often referred to as zinc dialkyldithiophosphates or simply zinc dithiophosphates. They are well known and readily available to those skilled in the art of lubricant formulation.
  • the amount of the metal salt of a phosphorus acid in a completely formulated lubricant, if present, may be 0.1 to 4, 0.5 to 2, or 0.75 to 1.25 percent by weight.
  • Additional performance additives which may be present in the compositions of the present invention include: metal deactivators, dispersants, antioxidants, antiwear agents, corrosion inhibitors, antiscuffing agents, extreme pressure agents, foam inhibitors, demulsifiers, friction modifiers, viscosity modifiers, pour point depressants and mixtures thereof.
  • metal deactivators include: metal deactivators, dispersants, antioxidants, antiwear agents, corrosion inhibitors, antiscuffing agents, extreme pressure agents, foam inhibitors, demulsifiers, friction modifiers, viscosity modifiers, pour point depressants and mixtures thereof.
  • fully- formulated lubricating oil will contain one or more of these performance additives.
  • Metal deactivators may be present including derivatives of ben- zotriazole, 1 ,2,4-triazoles, benzimidazoles, 2-alkyldithiobenzimidazoles, 2- alkyldithiobenzothiazoles, 2-(N,N-dialkyldithiocarbamoyl)benzothiazoles, 2,5- bis(alkyl-dithio)-l,3,4-thiadiazoles, 2,5-bis(N,N-dialkyldithiocarbamoyl)-l,3,4- thiadiazoles, and 2-alkyldithio-5-mercapto thiadiazoles.
  • the metal deactivator is 5-methylbenzotriazole (tolyltriazole).
  • Additional dispersants may be present including N-substituted long chain alkenyl succinimides such as polyisobutylene succinimide derived from polyisobuty- lene with a number average molecular weight in the range 350 to 5000 or 500 to 3000.
  • the invention further comprises at least one dis- persant derived from polyisobutylene succinimide derived from polyisobutylene with number average molecular weight in the range 350 to 5000 or 500 to 3000.
  • Another class of ashless dispersants is the Mannich bases.
  • Mannich dispersants are the reaction products of alkyl phenols with aldehydes and amines where the alkyl group typically contains at least 30 carbon atoms.
  • Antioxidants may be present, including diphenylamines, hindered phenols, molybdenum dithiocarbamates, sulphurised olefins and mixtures thereof.
  • Phenolic antioxidants include butyl substituted phenols containing 2 or 3 t-alkyl groups, especially t-butyl groups. The para position of the phenol may also be occupied by a hydrocarbyl group, including an ester-containing group or a group bridging two aromatic rings.
  • Antioxidants also include: aromatic amines, such as an alkylated diphenylamine such as nonylated diphenylamine, including mixtures of di-nonylated amine and mono-nonylated amine; sul- furized olefins, such as mono-, or disulfides or mixtures thereof; and molybde- num compounds. These materials can serve other functions as well, such as antiwear agents.
  • aromatic amines such as an alkylated diphenylamine such as nonylated diphenylamine, including mixtures of di-nonylated amine and mono-nonylated amine
  • sul- furized olefins such as mono-, or disulfides or mixtures thereof
  • molybde- num compounds molybde- num compounds.
  • Corrosion inhibitors may be present, including amine salts of car- boxylic acids such as octylamine octanoate (octylamine salt of octanoic acid), condensation products of dodecenyl succinic acid or anhydride and a fatty acid such as oleic acid with a polyamine, and half esters of alkenyl succinic acids with alkenyl containing 8 to 24 carbon atoms reacted with polyglycols.
  • car- boxylic acids such as octylamine octanoate (octylamine salt of octanoic acid)
  • condensation products of dodecenyl succinic acid or anhydride and a fatty acid such as oleic acid with a polyamine
  • half esters of alkenyl succinic acids with alkenyl containing 8 to 24 carbon atoms reacted with polyglycols amine salts of car- boxy
  • Antiscuffing agents may be present including organic sulfides and polysulfides, such as benzyldisulfide, bis-(chlorobenzyl) disulphide, dibutyl tetrasulfide, di-tertiary butyl polysulfide, sulfurized sperm oil, sulfurized methyl ester of oleic acid, sulfurized alkylphenol, sulfurized dipentene, sulfurized terpene, sulfurized Diels-Alder adducts, alkyl sulfenyl N'N-dialkyl dithiocarbamates, the reaction product of polyamines with polybasic acid esters, chlorobutyl esters of 2,3-dibromopropoxyisobutyric acid, acetoxymethyl esters of dialkyl dithiocarbamic acid and acyloxyalkyl ethers of xanthogenic acids and mixtures thereof.
  • organic sulfides and polysulfides such as
  • EP agents may be present, including oil soluble sulphur- and chlorosulphur-containing EP agents, chlorinated hydrocarbon EP agents and phosphorus EP agents.
  • Foam inhibitors may be present including organic silicones such as polyacetates, dimethyl silicone, polysiloxanes, polyacrylates or mixtures thereof. Examples of foam inhibitors include poly ethyl acrylate, poly 2- ethylhexylacrylate, poly vinyl acetate and mixtures thereof.
  • Demulsifiers may be present including derivatives of propylene oxide, ethylene oxide, polyoxyalkylene alcohols, alkyl amines, amino alcohols, diamines or polyamines reacted sequentially with ethylene oxide or substituted ethylene oxides or mixtures thereof. Examples of demulsifiers include trialkyl phosphates, polyethylene glycols, polyethylene oxides, polypropylene oxides,
  • Pour point depressants may be present including: esters of maleic anhydride-styrene copolymers; polymethacrylates; polyacrylates; polyacryla- mides; condensation products of haloparaffin waxes and aromatic compounds; vinyl carboxylate polymers; and terpolymers of dialkyl fumarates, vinyl esters of fatty acids, ethylene-vinyl acetate copolymers, alkyl phenol formaldehyde condensation resins, alkyl vinyl ethers and mixtures thereof.
  • Friction modifiers may be present including fatty amines and esters including glycerol esters such as glycerol monooleate, borated glycerol esters, fatty phosphites, fatty acid amides, fatty epoxides, borated fatty epoxides, alkoxylated fatty amines, borated alkoxylated fatty amines, metal salts of fatty acids, sulfurized olefins, fatty imidazolines, condensation products of carbox- ylic acids and polyalkylene-polyamines, and amine salts of alkylphosphoric acids.
  • glycerol esters such as glycerol monooleate, borated glycerol esters, fatty phosphites, fatty acid amides, fatty epoxides, borated fatty epoxides, alkoxylated fatty amines, borated alkoxylated fatty amines, metal
  • Viscosity modifiers may be present including hydrogenated styrene- butadiene rubbers, ethylene-propylene copolymers, polyisobutenes, hydrogenated styrene-isoprene polymers, hydrogenated radical isoprene polymers, polyme- thacrylate acid esters, polyacrylate acid esters, polyalkyl styrenes, alkenyl aryl conjugated diene copolymers, polyolefms, poly alky lmethacrylates, esters of maleic anhydride-styrene copolymers and mixtures thereof.
  • the lubricating composition of the present invention is useful for an internal combustion engine, for example stationary combustion engine, such as a power station combustion engine; a diesel fuelled engine, a gasoline fuelled engine, a natural gas fuelled engine or a mixed gasoline/alcohol fuelled engine.
  • the internal combustion engine is a 4-stroke and in another embodiment a 2-stroke engine.
  • the diesel fuelled engine is a marine diesel engine.
  • the present invention also includes methods of operating engines, such as marine diesel engines and power station combustion engine, by lubri- eating them with the compositions of the present invention. These methods include the steps of operating an engine and supplying the compositions described above to the engine.
  • compositions of the present invention are used as a system oil and/or crankcase oil in a marine diesel engine.
  • the compositions of the present invention are not marine diesel engine cylinder oils and are not used in marine diesel engines as cylinder oils.
  • Suitable marine diesel engines for use with the compositions and methods of the present are not overly limited. Suitable engines include 4- stroke trunk piston engines as well as 2-stroke cross-head engines that utilize a system oil. The use of the lubricating oil composition can impart one or more of improved cleanliness decreased cylinder wear, reduced deposits and reduced "black paint" build-up.
  • the invention also includes a process to prepare the lubricating compositions of the present invention, comprising mixing: (a) an oil of lubricat- ing viscosity; (b) an asphaltene dispersant comprising a cyclic headgroup that contains a nitrogen atom and at least one other heteroatom; and (c) a detergent derived from an alkyl phenol.
  • the mixing conditions are typically 15°C to 130 0 C, 20 0 C to 120 0 C or even 25°C to HO 0 C; and for a period of time in the range 30 seconds to 48 hours, 2 minutes to 24 hours, or even 5 minutes to 16 hours; and at pressures in the range 86.4 kPa to 266 kPa (650 mm Hg to 2000 mm Hg), 91.8 kPa to 200 kPa (690 mm Hg to 1500 mm Hg), or even 95.1 kPa to 133 kPa (715 mm Hg to 1000 mm Hg).
  • the process optionally includes mixing other performance additives as described above into the composition.
  • the optional performance additives can be added sequentially, separately or as a concentrate.
  • the present invention is in the form of a concentrate (which can be combined with additional oil to form, in whole or in part, a finished lubricant), the ratio of each of the above-mentioned dispersant, as well as other components, to diluent oil is typically in the range of 80:20 to 10:90 by weight.
  • the additives of the present invention may be prepared by reacting a substantially linear compound that contains at least one oxygen atom and at least two nitrogen atoms where the nitrogen atoms are separated by two or three carbon atoms, wherein the compound reacts with itself to form a ring structure containing the two nitrogen atoms.
  • the substantially linear compound itself may be derived from the reaction of a compound containing at least one -COOR group and a compound containing at least two nitrogen atoms where the nitrogen atoms are separated by two or three carbon atoms and where
  • R can be a hydrogen or a hydrocarbyl group, which may include one or more hetero atoms.
  • the substantially linear compound is derived from a fatty acid, such as a carboxylic acid, reacted with a compound contain- ing at least two nitrogen atoms where the nitrogen atoms are separated by two or three carbon atoms.
  • the carboxylic acid used to prepared the substantially linear compound has the structure: R -O-C(O)-R where each R and R is independently a hydrogen or a hydrocarbyl group, In some embodiments R contains from 1 to 250, 5 to 200, 10 to 50 or 16 to 20 carbon atoms. R may be derived from oleic acid or tallowic acid.
  • the nitrogen containing compound reacted with the fatty acid has a structure: (R')(R')N-R"-N(R')-R"-Y where Y is -N(R')(R') or -OR' and each R' is independently a hydrogen or a hydrocarbyl group, and each R" is independently a hydrocarbyl group.
  • suitable compounds include diethylenetriamine, aminoethyl ethanolamine, N,N-dimethylaminopropyl aminopropylamine, a polyisobutylene succinimide dispersant and combinations thereof.
  • the substantially linear compound is derived from a compound containing at least two nitrogen atoms where the nitrogen atoms are separated by two or three carbon atoms reacted with an oxygen containing compound.
  • the nitrogen containing compound may be a polyamine, such as Nl -coco-propane- 1 ,3 -diamine, l-(3-aminopropyl)-imidazole, N- tallowpropyldiamine, N-dodecylpropylamine, or combinations thereof.
  • the oxygen containing compound may generally have the structure: R' -0-C(O)- (CH 2 ) n [C(O)] m -O-R" where R' is hydrogen or a hydrocarbyl group, n is 0, 1 or 2, m is 0 or 1, and R" is a hydrogen or a hydrocarbyl group.
  • Suitable examples include gly colic acid, diethyl carbonate, and even polyisobutylene succinic anhydride, guanidine carbonate, and combinations thereof.
  • asphaltene dispersants of the present invention may go through one or more intermediate structures before reaching the desired structure.
  • These intermedi- ate structures may include any of the structures represented by the following formulas:
  • each R 2 is independently hydrogen or a hydrocarbyl group comprising 1 to 50 carbon atoms; each R 3 is independently a hydrocarbyl group containing 1 to 50 carbon atoms; each R 4 is a hydrocarbyl group containing 1 to 200 carbon atoms; and X is a hydrocarby- lene group derived from an amine or a polyamine comprising 1 to 20 carbon atoms and 1 to 5 nitrogen atoms.
  • compositions of the present invention include the asphaltene dispersants described above in combination with the one or more of the intermediates described above. All of these materials, including the intermediates can provide improved performance, particularly over the starting succinimide often used to prepare them.
  • hydrocarbyl and “hydrocarbylene” as used with respect to groups and or substituents are used in their ordinary sense, which is well-known to those skilled in the art. Specifically, these terms all refer to a group having a carbon atom directly attached to the remainder of the molecule and having predominantly hydrocarbon character.
  • hydrocarbyl and hydrocarbylene groups include: hydrocarbon substituents and/or connecting groups, 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); substituted hydrocarbon substituents, that is, substituents containing non-hydrocarbon groups which, in the context of this invention, do not alter the predominantly hydrocarbon nature of the sub- stituent (e.g., halo (especially chloro and fluoro), hydroxy, alkoxy, mercapto, alkylmercapto, nitro, nitroso, and sulfoxy); hetero substituents, that is, substituents,
  • Heteroatoms include sulfur, oxygen, nitrogen, and encompass substituents as pyridyl, furyl, thienyl and imidazolyl.
  • substituents as pyridyl, furyl, thienyl and imidazolyl.
  • no more than two, preferably no more than one, non-hydrocarbon substituent will be present for every ten carbon atoms in the hydrocarbyl group; typically, there will be no non-hydrocarbon substituents in the hydrocarbyl group.
  • An asphaltene dispersant is prepared by charging oleic acid (50 grams), toluene (50 grams) and Nl-(3-dimethylamino-propyl)-propane-l ,3- diamine (29.63 grams) to a 250 ml round bottom flask (Flask A) for reaction, equipped with overhead stirrer, heating mantle, thermocouple, Dean-Stark trap water cooled condenser and nitrogen inlet. The materials are mixed in the flask at 250 rpm and warmed to 100 0 C. The mixture is held with mixing for 1 hour and then warmed to 110 0 C and held with mixing overnight.
  • oleic acid 50 grams
  • toluene 50 grams
  • Nl-(3-dimethylamino-propyl)-propane-l ,3- diamine 29.63 grams
  • the mixture is then warmed to 120 0 C and held with mixing for 1 hour, warmed to 130 0 C and held with mixing for 1 hour, warmed to 135°C and held with mixing overnight, warmed to 140 0 C and held with mixing for 1 hour, warmed to 150 0 C and held with mixing overnight.
  • the reaction mixture is then cooled and allowed to stand over the weekend.
  • the reaction mixture is then warmed to 160 0 C and held with mixing for 1 hour, warmed to 170 0 C and held with mixing for 1 hour, warmed to 185°C and held with mixing for 30 hours.
  • the reaction is monitored by IR checking for a large amide peak with amidine peak shoulder at 1646 cm 1 .
  • the collected product (71.81 grams) is a pale yellow liquid
  • the collected product (61.4 grams) is then charged to a 250 ml 3- neck round bottom flask (Flask B), equipped with Dean-Stark trap and water cooled condenser, magnetic stirrer, heating mantle and thermocouple, and nitrogen inlet.
  • the material is warmed to 200 0 C with mixing at 100 rpm and held for 0.5 hours to allow the system to equilibrate.
  • the material is then warmed to 210 0 C and held with mixing for 1.5 hours.
  • the material is allowed to cool to room temperature overnight and then is warmed to 220 0 C and held with mixing for 4 hours.
  • the material is then cooled to 100 0 C and collected.
  • the process is monitored by IR checking for an increase in peak intensity at
  • the resulting material (61.4 grams) is a viscous clear orange oil with a total base number (TBN) of 216 mg KOH/g.
  • TBN total base number
  • the resulting material contains a 2-alkyl-tetrahydro-pyrimidine, specifically 2-oleyl-l-(3- dimethylaminopropyl)-l,4,5,6-tetrahydro-pyrimidine.
  • An asphaltene dispersant is prepared by charging oleic acid [2-(2- hydroxy-ethylamino)-ethyl]-amide (83.29 grams), to a 250 ml flask, equipped as Flask B described above. The material is warmed to 200 0 C with stirring at 100 rpm for 0.5 hours. The material is then warmed to 220 0 C and held with mixing for 2 hours. The material is allowed to cool to room temperature overnight. The material is then warmed to 220 0 C and held with mixing for 4 hours. The material is then cooled to 100 0 C and collected.
  • the process is monitored by IR checking for an increase in peak intensity at 1605 cm “1 (for the amidine) and a decrease in peak intensity at 1650 cm “1 (for the amide).
  • the resulting material (73.6 grams) is a viscous clear orange oil with a TBN of 149 mg KOH/g.
  • the resulting material contains a 2-alkyl-imidazoline, specifically 2-oleyl-l-(2-hydroxyethyl)-imidazoline.
  • An asphaltene dispersant is prepared according to the procedure of Example 1, except that Nl -tallow-propane- 1 ,3 -diamine (50 grams), toluene (50 grams) and glycolic acid (11.75 grams) are charged to the reaction flask.
  • the first part of the process, in the Flask A system results in 50.22 grams of a waxy solid.
  • the second part of the process, in the Flask B system results in 34.32 grams of a 1-alkyl-tetrahydro-pyrimidine, specifically (1-tallow-l, 4,5,6- tetrahydropyrimidin-2-yl)methanol.
  • An asphaltene dispersant is prepared by charging polyisobutylene succinic anhydride (PIBSA), derived from polyisobutylene having a number average molecular weight (Mn) of 2300, (502.5 grams) to a 1 litre reaction flask, equipped similarly to Flask A described above. The material is heated to 150 0 C under nitrogen with mixing at 350 rpm. l-(3-aminopropyl)-imidazole (22.8 grams) is then added to the flask dropwise over 0.5 hours. After the feed is complete, the reaction mixture is held at 150 0 C for 3.5 hours. The reaction is monitored by IR checking for a large imide peak at 1702 cm "1 . The resulting material (515.5 grams) is a dark brown material and contains a 1- alkylimidazole, specifically (l-polyisobutenesuccinimidylpropyl)imidazole.
  • PIBSA polyisobutylene succinic anhydride
  • An asphaltene dispersant is prepared by charging Nl-coco-propane- 1,3-diamine (55.36 grams) and diethyl carbonate (29.45 grams) to a 250 ml reaction flask, equipped as Flask A described above. The mixture is heated to 100 0 C under nitrogen with mixing at 300 rpm. The mixture is held at tempera- ture with mixing for 16 hours and is then warmed to 135°C and held with mixing for 5 hours, then warmed to 150 0 C and held with mixing for 3 hours.
  • the mixture is then cooled to room temperature, and then warmed to 120 0 C and held with mixing for 16 hours, then warmed to 180 0 C and held with mixing for 2 hours, then warmed to 190 0 C and held with mixing for 1 hour.
  • the reaction is monitored by IR.
  • the resulting material (51.09 grams) is a white, soft waxy solid and contains a l-alkyl-tetrahydro-pyrimidin-2-one, specifically 1-coco- tetrahydro-pyrimidin-2-one.
  • An asphaltene dispersant is prepared by charging DuomeenTM O (1126 grams), iminodiacetic acid (228.9 grams), and xylene (1500 ml) to a 5-liter round bottom flask equipped with a mechanical overheard stirrer, ther- mocouple and heating mantle, sub-surface nitrogen sparge line, and Dean-Stark trap with condenser. A polydimethylsiloxane is added (6 drops) and the mixture is heated, with stirring, to 145°C over 4.5 hours.
  • the mixture is then held at 150 0 C for 2 hours, then held at 155°C for 2.5 hours, then held at 160 0 C for 1.5 hours, then held at 170 0 C for 1.5 hours, then held at 180 0 C for 1.5 hours, then held at 200 0 C for 6.5 hours, then held at 220 0 C for 16 hours, and then held at 230 0 C for 8 hours, distilling off xylene as the temperature increases.
  • the flask is allowed to cool and is held at various points overnight, resuming the next day at the same point.
  • the resulting material (1175 grams) is cooled and collected.
  • An asphaltene dispersant is prepared by charging DuomeenTM T (2504.6 grams) and ethylene glycol (437.6 grams) to a 5-liter round bottom flask equipped as described in Example 5 above. The material is heated to 105 0 C with stirring. Ethylene carbonate (620.67) is added over 1 hour with the mixture exotherming to 108 0 C. The mixture is then held at 105 0 C, with mixing, for 1 hour, then held at 130 0 C for 5 hours, then held at 180 0 C for 6.5 hours. The mixture is then vacuum distilled at 180 0 C and about -0.9 bar for 3 hours in order to remove the ethylene glycol solvent. The flask is allowed to cool and is held at various points overnight, resuming the next day at the same point. The resulting material (2654.5 grams) is cooled and collected.
  • An asphaltene dispersant is prepared by charging diethylenetriamine (164.65 grams) and toluene (350 ml) to a 1 liter reaction flask, equipped similarly to Flask A described above. The mixture is heated to 100 0 C with mixing. The mixture is then heated to 135°C and oleic acid (151.11 grams) is added dropwise over 5 hours. The mixture is then heated to 135°C and held, with mixing, for 17 hours. Excess toluene and diethylenetriamine is vacuum stripped from the flask at 135°C and about -0.9 bar over 3 hours. The flask is allowed to cool and is held at various points overnight, resuming the next day at the same point. The resulting material (169.9 grams) is cooled and collected. Example 9
  • An asphaltene dispersant is prepared by charging oleic acid (300 grams) and toluene (100 grams) to a 1 liter reaction flask, equipped similarly to Flask A described above. The mixture is heated to 125°C with stirring and aminoethyl ethanolamine (1 10.6 grams) is then added over 1 hour. The reaction mixture is then heated to 135°C and held, with mixing, for 2 hours, then heated to 170 0 C over 1 hour, collecting and removing distillate from the system, then warmed to 210 0 C and held, with stirring, for 2 hours, then heated to 215°C and held, with stirring, for 3 hours. The reaction mixture is then vacuum distilled at 215°C and 100 mbar for 0.5 hours. The resulting material (363.45 grams) is cooled and collected.
  • An asphaltene dispersant is prepared by charging oleic acid (300 grams) and toluene (100 grams) to a 1 liter reaction flask, equipped similarly to Flask A described above. The mixture is heated to 100 0 C with stirring and N,N-dimethylaminopropyl aminopropylamine (100 grams) is then added over 1 hour.
  • the reaction mixture is then held for 0.5 hours, and then heated to 130 0 C and held, with mixing, for 0.5 hours, then heated to 150 0 C and held for 1 hour, then warmed to 175°C and held, with mixing, overnight, then warmed to 200 0 C and held for 1 hour, then warmed to 215°C and held for 1 hour, then warmed to 220 0 C and held for 3 hours.
  • the reaction mixture is then vacuum distilled at temperature for 5 hours.
  • the resulting material (386.11 grams) is cooled and collected.
  • An asphaltene dispersant is prepared by charging a polyisobutenyl succinimide dispersant, derived from 1000 Mn PIBSA and tetraethylene pen- tamine, (475.5 grams) to a 1 liter reaction flask, equipped similarly to Flask A described above. The material is heated to 175°C with stirring and held for 1 hour. The material is cooled to 100 0 C and tall oil fatty acid (43.9 grams) is added over 6 minutes. The mixture is then heated, with stirring, to 230 0 C over 0.5 hours and then held for 22 hours. The resulting material (503.4 grams) is cooled and collected.
  • An asphaltene dispersant is prepared by charging DuomeenTM T (300 grams) and glycolic acid (70.42 grams) to a 1 liter reaction flask, equipped similarly to Flask A described above. The material is heated to 140 0 C with stirring and held for 24 hours. The material is then heated to 220 0 C and held for 8 hours, and then cooled and held at room temperature overnight. The material (310.68 grams) is then collected and is a dark brown waxy solid at room temperature.
  • An asphaltene dispersant is prepared by charging DuomeenTM T (300 grams) to a 1 liter reaction flask, equipped similarly to Flask A described above. The material is heated to 1 10 0 C with stirring and guanidine carbonate
  • reaction mixture is then cooled to 120 0 C and filtered using
  • Formulation A is a salicylate-free formulation
  • Formulation B contains a mixture of salicylate and phenate detergents. All formulations contain 4 percent by weight of the dispersant being evaluated, are in the same base oils, and each example has a total base number (TBN) of 40.
  • Mn number average molecular weight
  • PIB polyisobutylene
  • 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.
  • the amount of each chemical component is presented exclusive of any solvent or diluent oil, which may be customarily present in the commercial material, unless otherwise indicated.
  • the upper and lower amount, range, and ratio limits set forth herein may be independently com- bined.
  • the ranges and amounts for each element of the invention can be used together with ranges or amounts for any of the other elements.
  • the expression "consisting essentially of permits the inclusion of substances that do not materially affect the basic and novel characteristics of the composition under consideration.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La présente invention porte sur une composition lubrifiante, en particulier sur des compositions lubrifiantes pour moteurs diesel marins, comprenant : (a) une huile de viscosité lubrifiante ; (b) un dispersant des asphaltènes comprenant un groupe de tête cyclique qui contient un atome d'azote et au moins un autre hétéroatome ; et (c) un détergent issu d'un alkyl phénol. L'invention porte également sur des procédés d'utilisation de ces compositions dans le fonctionnement de moteurs diesel en particulier de moteurs diesel marins.
PCT/US2010/043490 2009-08-06 2010-07-28 Compositions lubrifiantes contenant un dispersant des asphaltènes WO2011017148A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
EP10744628A EP2462212A1 (fr) 2009-08-06 2010-07-28 Compositions lubrifiantes contenant un dispersant des asphaltènes
CN201080044666.7A CN102575185B (zh) 2009-08-06 2010-07-28 含沥青质分散剂的润滑组合物
KR1020127005681A KR101811891B1 (ko) 2009-08-06 2010-07-28 아스팔텐 분산제를 함유하는 윤활 조성물
SG2012007050A SG178205A1 (en) 2009-08-06 2010-07-28 Asphaltene dispersant containing lubricating compositions
JP2012523652A JP5823392B2 (ja) 2009-08-06 2010-07-28 アスファルテン分散剤含有潤滑組成物
CA2770160A CA2770160A1 (fr) 2009-08-06 2010-07-28 Compositions lubrifiantes contenant un dispersant des asphaltenes
US13/388,333 US20120266837A1 (en) 2009-08-06 2010-07-28 Asphaltene Dispersant Containing Lubricating Compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US23169409P 2009-08-06 2009-08-06
US61/231,694 2009-08-06

Publications (1)

Publication Number Publication Date
WO2011017148A1 true WO2011017148A1 (fr) 2011-02-10

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Country Status (8)

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US (1) US20120266837A1 (fr)
EP (1) EP2462212A1 (fr)
JP (2) JP5823392B2 (fr)
KR (1) KR101811891B1 (fr)
CN (1) CN102575185B (fr)
CA (1) CA2770160A1 (fr)
SG (1) SG178205A1 (fr)
WO (1) WO2011017148A1 (fr)

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CN102866227A (zh) * 2011-07-07 2013-01-09 卢布里佐尔公司 烟灰小型试验
GB2496732A (en) * 2011-11-17 2013-05-22 Infineum Int Ltd Marine engine lubrication
US11725132B2 (en) 2016-12-30 2023-08-15 Stepan Company Compositions to stabilize asphaltenes in petroleum fluids

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KR102242740B1 (ko) * 2013-09-19 2021-04-21 더루우브리졸코오포레이션 직접 분사 엔진용 윤활제 조성물
US9909079B2 (en) * 2013-10-18 2018-03-06 Chevron Oronite Company Llc Lubricating oil composition for protection of silver bearings in medium speed diesel engines
CN104312703A (zh) * 2014-11-14 2015-01-28 柳州聚龙科技有限公司 船舶用润滑油
EP3253856A1 (fr) 2015-02-06 2017-12-13 The Procter and Gamble Company Produit de consommation comprenant des hydrocarbures modifiés par un amino
US20160229929A1 (en) * 2015-02-06 2016-08-11 The Procter & Gamble Company Amino Modified Hydrocarbons
WO2016138227A1 (fr) * 2015-02-26 2016-09-01 The Lubrizol Corporation Détergents aromatiques et compositions lubrifiantes de ceux-ci
US10655052B2 (en) 2016-12-30 2020-05-19 M-I L.L.C. Method and process to stabilize asphaltenes in petroleum fluids
KR102299697B1 (ko) * 2019-05-09 2021-09-08 한국화학연구원 양극성 첨가제를 이용한 악취 및 유해물질이 저감된 아스팔트 제조 공정
CN110129114A (zh) * 2019-06-04 2019-08-16 王保亮 一种发动机保护剂

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Publication number Priority date Publication date Assignee Title
CN102866227A (zh) * 2011-07-07 2013-01-09 卢布里佐尔公司 烟灰小型试验
GB2496732A (en) * 2011-11-17 2013-05-22 Infineum Int Ltd Marine engine lubrication
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GB2496732B (en) * 2011-11-17 2014-03-12 Infineum Int Ltd Marine engine lubrication
US11725132B2 (en) 2016-12-30 2023-08-15 Stepan Company Compositions to stabilize asphaltenes in petroleum fluids

Also Published As

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JP5823392B2 (ja) 2015-11-25
CA2770160A1 (fr) 2011-02-10
US20120266837A1 (en) 2012-10-25
JP2013501127A (ja) 2013-01-10
KR20120055593A (ko) 2012-05-31
CN102575185A (zh) 2012-07-11
CN102575185B (zh) 2014-03-05
SG178205A1 (en) 2012-03-29
EP2462212A1 (fr) 2012-06-13
KR101811891B1 (ko) 2017-12-22
JP2015193856A (ja) 2015-11-05

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