CA1306741C - Low phosphorus lubricants - Google Patents

Low phosphorus lubricants

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Publication number
CA1306741C
CA1306741C CA000560012A CA560012A CA1306741C CA 1306741 C CA1306741 C CA 1306741C CA 000560012 A CA000560012 A CA 000560012A CA 560012 A CA560012 A CA 560012A CA 1306741 C CA1306741 C CA 1306741C
Authority
CA
Canada
Prior art keywords
copper
oil
composition
soluble
sulphur
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CA000560012A
Other languages
French (fr)
Inventor
Terence Coclough
John Frederick Marsh
Frederick Alastair Gibson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Chemical Patents Inc
Original Assignee
Exxon Chemical Patents Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Publication of CA1306741C publication Critical patent/CA1306741C/en
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Abstract

ABSTRACT
Low Phosphorus Lubricants Lubricants having antiwear, corrosion inhibition and antioxidant performance appropriate to modern oil requirements with reduced or zero amounts of phosphorous and without the need for large amounts and/or expensive forms of antioxidant comprise 5 to 500 parts per million by weight (ppm) of added copper present in oil-soluble form, one or more added oil-soluble sulphur-containing compounds and a bearing corrosion inhibitor.

Description

L ~

Low Phos~horus Lubricants The present invention relates to lubricating coMpositions, e~pecially automobile crankcase lubricants, containing low or zero amounts of phosphorus.

There is currently a drive to reduce the amounts of phosphorus in lubricants because of the deleterious effect phosphorus has on catalysts commonly used in catalytic converters used for emission control. Levels of phosphorus have typically been of the order of 0.1% but there is an increasing need ~o reduce phosphorus levels to below 0.05 wt ~ or remove it altogether.
However; zinc dialkyl dithiophosphates (ZDDP) and other phosphorus containing additives have been widely used as anti-wear and/or anti-oxidant additives and simply reducing or removing such components results in lubricants with poor engine performance.

This invention provides lubricant compositions and concentrates with low or zero phosphorus contents which comprise copper, sulphur, and a bearing corrosion inhibitor, which compositions have been found to have remarkable engine performance.

US-A-2356661 deals with lubricating oils containing 50 to lO00 parts per million of copper as an oil-soluble organic compound such as copper dialkyl dithiocarbamates and including phosphorus containiny compounds together with from 0.1 to 0.5 wt ~ of total sulphur in the oil, sulphur being provided as oil-soluble organic sulphur compounds such as thiocarbamates.

US-A-2343756 discloses the addition of copper co~pounds including phosphorus-containing copper complexes in conjunction with sulphur compounds, to lubricating oils. Amounts of from 0.1 to 0.5 wt % of sulphur are disclosed, with amounts in excess of 0.5 wt % sulphur described as being potentially detrimental. In VS-A-2552580, cuprous thiophosphates are included in lubricant compositions at relatively high levels, which will give high phosphorus level in the oils.
,~

~3~

In US-A~3346493, a wide variety of metal-containing poly~eric amine metal reactants are employed as detergents in lubricant compositions. In an isolated example, a lubricant is described containing inter alia, a copper salt of an acylated nitrogen compound, 0.075% phosphorus as a ZDDP reacted with hexene oxide, and a sulphurized methyl ester of a tall oil acid.
Other copper containing lubricants either contain more phosphorus or no sulphur. US-A-4122033 discloses the entire group of transition metal compounds as antioxidation stabilizers in conjunction with amines, selenides, phosphines or phosphites and may be used in various applications including as additives for lubricants. None of the foregoing documents describe fully formulated lubricant oils which would be appropriate to meet the requirements for modern lubricants and none specifically address the reduction of phosphorus levels while maintaining performance in antiwear, antioxidation and corrosion inhibition.

EP-A-24146 discloses lubricant compositions containing an ashless dispersant and/or polymeric viscosity index improver dispersant and copper which may be in the form of a dithiocarbamate, but requires the presence of zinc and from 0.01 to 0.5 wt % phosphorus. Thiadiazole polysulphides are an optional component.

US-A-4330420 describes oils with reduced phosphorus content (but only to 0.05%P) using mixtures of dialkyldiphenylamine and a sulphurized polyolefin to compensate for reduction in the amount of ZDDP. There is no disclosure of the use of copper or thiadiazole polysulphides.

EP-A-89844 describes reaction products of 4,4'-methylene bis(2,6-di-t~butyl phenol) and tri-Sec-C4_12 alkyl orthoborate and their use in lubricants to enable the amount of ZDDP to be reduced to provide from 0.05 to 0.11 wt g P.

_ 3 ~ ~3~

US-A-4490265 describes lubricating oils comprising boron-containing heterocyclic compounds which may be in the form of a metal salt including a copper salt, thiadiazole polysulphides, terephthalic acid and as an vxidation inhibitor either a bis(dithiobenzil) metal derivative where the metal may inter alia be copper or a sulphur-bridged, bis hindered phenol. The desirability of reducing or eliminating phosphorus is not disclosed and all the Examples of lubricants contain 0.05 wt% P. US-A-4623474 makes a similar disclosure.

VS-A-4627930 also describes boron-containing heterocyclic compounds which may be in the form of a copper salt and may be sulphurized. Thiadiazole polysulphides and copper carboxylates are also disclosed. Although the boron containing heterocyclic compounds are described as phosphorus-free, there is no disclosure of a fully formulated oil containing less than 0.05 wt % P. US-A-4629580 contains a similar disclosure.
US-A-4629579 discloses boron and metal-boron derivatives for use as extreme pressure, anti-wear and friction reducing additives for lubricating oils, and compositions including one containing no ZDDP, but there is no disclosure of a composition containing low or zero amounts of phosphorus, with sulphur and copper.

Lubricant compositions containing low, or zero amounts of phosphorus, but no copper are described in WO-A-8604601, WO-A-8604602 and WO-A-8606092.

The invention seeks to provide lubricants having antiwear, corrosion inhibition and antioxidant performance appropriate to modern oil requirements with reduced or zero amounts of phosphorous and without the need for large amounts and/or expensive forms of antioxidant.

The term ~Modern oil~ as used herein in relation to automobile crankcase lubricants refers to oil which can meet the current requirements for crankcase lubricants in the major industrial countries. ~igh performance engines, increased lifetime _ 4 _ ~3~

requirements resulting from longer periods between oil changes, and higher opeeating temperatures all contribute to the increased performance required from lubricants. This invention is particularly concerned with automobile crankcase lubricants which can meet and exceed the requirements for the SF API
Engine Service Category for service station oils and/or the requirements for the CD API Engine Service Category for Commercial Oils/Diesel Engines, established jointly by API, SAE
and ASTM.

In one aspect, this invention provides a lubricant composition comprising a major a~ount of a lubricating oil/ 5 to 500 parts per million by weight (ppm) of added copper present in oil-soluble form, one or more added oil-soluble sulphur-containing compounds such that the composition preferably comprises from greater than 0.5 to 2.0 wt % of total sulphur, more preferably 0.5 to 1.0 wt % of total sulphur and an effective amount o~ a bearing corrosion inhibitor, the composition containing less than 0.01 wt % phosphorus, preferably being substantially phosphorus-free.

In particularly preferred embodiments of the invention, the lubricant composition will also contain one or more ashless dispersants and/or one or more viscosity index improver dispersants and/or one or more overbased additives which function as antacid and anti-rust agents, such as overbased calcium or magnesium sulphonates or phenates.

The use of copper in the invention enables a low phosphorus oil with performance meeting the re~uirements of modern oils to be obtained economically and with good control of oxidation, which in an automobile engine is catalysed by metal accumulated in the oil by wear or corrosion, with iron being a particular oxidation catalyst. At unduly low concentrations of copper, the anti-oxidant effect may not be sufficient for some applications. At unduly high concentrations, the ash level of the oil will he increased and an increased tendancy to bearing corrosion may be observed. The amount of added copper in the compositions will generally be within the range of 10 to 400 ppm, typically 10 to 300 ppm, preferably 10 to 200 ppm, e.g. 60 to 200 ppm.

- 5 - ~3~

The ability of the compositions of the invention comprising low amounts of oil-soluble copper compounds and very low or zero a~ounts of phosphorus to provide adequate antioxidant and antiwear performance for the stringent requirements of modern engine tests is surprising. Copper is known to act in many situations as an oxidation promoter or catalyst, and closely related metalsr such as cobalt and chromium, are not effective lubricant anti-oxidants. EP-A-24146 teaches the presence of at least 0.01 wt % of each of phosphorus and zinc.

It is also surprising that the copper compound functions effectively in compositions which may contain zinc and other metal compounds, such as calcium or magnesium overbased additivesl which have an inherent pro-oxidant activity.

The copper compounds used as ar.ti-oxidants in this invention may be chosen from those described in EP-A-24146 as suitable for lubricants provided that the copper compounds are substantially free of phosphorus.

Thus, the copper may be blended into the oil as the oil-soluble copper salt of a synthetic or natural carboxylic acid.
Examples of suitable carboxylic acids include Clo to Clg fatty acids such as stearic or palmitic acid, unsaturated acids such as oleic acid, branched carboxylic acids such as naphthenic acids of molecular weight fro~ 200 to 500, neodecanoic or 2-ethylhexanoic acid and alkyl or alkenyl substituted dicarboxylic acids such as polyalkene substituted succinic acids, e.g. octadecenyl succinic acids, dodecenyl succinic acids and polyisobutenyl succinic acids.

The copper may be blended into the oil as oil-soluble copper dithiocarbamates of the general formula (~R'NCSS~nCu~ where n is 1 or 2 and R and R' are the same or different hydrocarbyl radicals containing 1 to 18, preferably 2 to 12 carbon atoms such as alkyl, alkenyl, aryl, aralkyl/ alkaryl and cycloalkyl radicals. Other copper and sulphur containing compounds such as copper mercaptides, disulphides and thioxanthates are suitable for use in the invention. Copper sulphonates, phenates, and acetylacetonates may also be used.

- 6 - ~3~$~

Alternatively the copper may be introduced in the oil in an oi~ insoluble form provided that in the finished lubricant composition the copper is in the form on an oil-soluble compound. The term "added copper n is intended to exclude copper present in the oil as a result of accumulation of copper in the oil during use, e.g. by wear or corrosion of copper--containing components.

The lubricant compositions of the invention contain an added oil-soluble sulphur compound. one preferred class of such sulphur compounds are the dithiocarbamates, preferably of the formula: (RR'NCSS~n M, wherein R, R' and n are as defined hereinbefore and M is a suitable metal such as zinc, molybdenum or (as indicated above) copper or a optionally substituted hydrocarbyl radical. Preferred dithiocarbamates are dialkyl dithiocarbamates preferably containing 2 to 12 carbon atoms such as diamyl dithiocarbamates. A particularly preferred compound is zinc diamyl dithiocarbamate.

Sulphur may also be introduced as a mercaptide particularly the mercaptides of aliphatic mercaptans (including copper mercaptides as indicated above), sulphurized unsaturated organic compownds including sulphurized olefins (e.g.
US-A-4119549, ~S-A-4-4119550, US-A-4:L91659 and US-A-4147640), sulphurized Diels-Alder adducts (e.g. US-A~3632566, US-A-3498915 and US-E-27331) and particularly sulphurized unsaturated alcohols and esters such as sperm oil substitutes, e.g. sperm oil, sulphides including di- and polysulphides, thioethers, thiophenols/ thioxanthates ~including copper thioxanthates as indicated above), sulphurized esters, thioesters, thioamides, thia201es such as benzothiazoles and particularly mercaptobenzothiazoles, and thiadiazoles.

Mineral lubricating oils contain sulphur, whereas synthetic oils may be sulphur-free, so that the amount of sulphur added as a sulphur-containing compound varies according to the basestock and the sulphur contents of other components in the lubricating composition, more preferably so as to give a sulphur content of greater than 0.5 to 1~0 wt % total sulphur.

~ 7 ~ 13~7~
The lubricant compositions of the invention advantageously contain from 0.5 to 0.7 wt % total s, and most preferably 0.1 to 0.5 wt % S as added oil-soluble sulphur-containing compound. They also preferably contain 0.01 to 0.5 wt % zn, more preferably 0.05 to 0.2 wt % zn. In a particularly preferred aspect the compositions contain 0.5 to 3 wt % zinc dithiocarbamate.
.

The bearing corrosion inhibitor is a corrosion inhibitor effective at inhibiting corrosion effects on bearings such as Cu/Pb bearings, where effects such as copper staining and high weight loss can be encountered. Such additives have been found to promote the antiwear performance of the oil. Preferred bearing corrosion inhibitors are borate esters such as B(OR)3, (RO)2B-O-B(OR)2, (ROBO)3 (RO)2BORlOB(OR)2 and mixtures (wherein R is a substituted or unsubstituted alkyl, aryl or aralkyl group or two groups R form a substituted or unsubstituted alkylene group and Rl is a substituted or unsubstituted alkylene group) and these materials may be derived, for example, from alcohols such as alkoxyalkanols (both short chain alkanols and longer chain alcohols as in US A-4440656) and polyetheralkanols; mono-, di- and ~rihydroxy alkanols, e.g.
2-ethylhexanol, 2-ethylhexan-1, 3-diol, butane-1,2-diol butane-1,3-diol, glycerol and the acyclic polyols of US-A-2866811; hydroxy esters such as glyceryl mono-oleate oxazolines derived for example from oleic acid and tris(hydroxymethyl)-aminomethane; sulphur-containing alcohols such as may be obtained by reacting epoxides with mercaptans e.g. t-dodecyl-mercaptoethanol; amino alcohols such as alkanolamines e.g. triethanolamine and tri-isopropanolamine, hydroxyamines made by reacting a primary amine (e.g.
oleylamine) or secondary amine with ethylene or propylene oxide and the compounds of US-A-4406802. Preferred alcohols are 2-methylpentan-1,3-diol, butane-1,2-diol, butane-1,3-diol and similar 1,2 and 1,3 diols, and ethoxyethanol.

In a preferred aspect the invention contains from 0.01 to 10 wt %, preferably 0.1 to 5 wt %, of a borate ester especially an ester of an alkoxyalkanol or a polyetheralkanol, e.g. a tris(ethoxyethyl) orthoborate ester or metaborate ester, or a biborate of a diol such as butane-1,3-diol.

As an alternative, the bearing corrosion inhibitor is a thiadiazole mercaptan, especially a thiadiazole polysulphide containing from 5 to 50 caebon atoms, a derivative or polymer thereof. Preferred materials are the 1,3,4 thiadiazole polysulphides such as those described in US-A-2719125, 2719126 and 3087932. Especially preferred is the compound 2,5-bis (t-octadithio)-1,3,4-thiadiazole commercially available as Amoco 150 or 2,5-bis(nonyldithio)-1,3,4-thiadiazole avallable as Amoco 158. Other similar materials also suitable are described in US-A-3821236, 3904537, 4097387, 4107059, 4136043, 4188299 and 4193882. Derivatives of thiadiazole mercaptans may be used such as esters, condensation products with halogenated carboxylic acids, reaction products with aldehydes and amines, alcohols or mercaptansl amine salts, dithiocarbamates, reaction products with ashless dispersants (e.g. US-A-4140643 and US-A-4136043) and reaction products with sulphur halides and olefins.

These materials are preferably present in an amount of from 0.01 to 10 wt ~, more preferably 0.1 to 5O0 wt % of the lubricant composition.

The lubricating compositions may comprise small amounts of phosphorus, less than 0.01 wt %, preferably less than 0.005 wt %7 but more preferably the lubricating compositions are substantially free of phosphorus.

In a preferred aspect the lubricating composition further comprises:

(A) from 1 to 10 wt % of an ashless dispersant compound which i s :
an ashless nitrogen or ester containing dispersant compound preferably selected from:

(i) oil soluble salts~ amides, imides, oxazolines and esters~
or mixtures thereof, of long chain hydrocarbon substituted mono and dicarboxylic acids or their anhydrides;

a~em~

6t~

~ii) long chain aliphatic hydrocarbon having a polyamine attached directly thereto; and (iii) Mannich condensation products formed by condensing a molar proportion of long chain hydrocarbon substituted phenol with 1 to 2.5 moles of formaldehyde and 0.5 to 2 moles of polyalkylene polyamine;
wherein said long chain hydrocarbon group is a polymer of a Cz to C5 monoolefin, said polymer having a molecular weight of 700 to 5000; and/or (B) from 0.3 to 10 wt %, of a nitrogen or ester containing polymeric viscosity index improver dispersant which may include (a) polymers comprised of C4 to C24 unsaturated esters of vinyl alcohol or C3 to Clo unsaturated mono- or di-carboxylic acid with unsaturated nitrogen containing monomers having 4 to 20 carbons;
(b) polymers of C2 to C20 olefin with unsaturated C3 to Clo mono- or di-carboxylic acid neutralised with amine, hydroxy amine or alcohols; and (c) polymers of ethylene with a C3 to C20 olefin further reacted either by grafting C~ to C20 unsaturated nitrogen containing monomers thereon or by yrafting an unsaturatecl acid onto the polymer backbone and then reactin~ said carboxylic acid groups with amine, hydroxy amine or alcohol.

The nitrogen containing dispersant additives are those known in the art as sludge dispersants for crankcase motor oils, eOg.
such as shown in US-A-3275554, US-A-3565804, US-A-3442808, US-A-3442808, GB-A-983040 or BE-A-658236.

The most commonly used dispersants are those formed by reacting alkenyl succinic anhydride, e.g. polyisobutenyl succinic anhydride, and an amine described in US-A-3202678, 3154560~
3172892, 3024195, 3024237, 3219666, 3216936 and BE-A-662875.

~L3~6~

Alternatively the ashless dispersants may he esters derived from long chain hydrocarbon substituted carboxylic acids and from hydroxy compounds such as monohydric and polyhydric alcohols or aromatic compounds such as phenols and naphthols as prepared for example in US-A-3522179.

Hydroxyamines which can be reacted with any of the aforesaid long chain hydrocarbon substituted carboxylic acids to form dispersants include 2-amino-1-butanol, 2-amino-2-methyl-1-propanol, p-(beta-hydroxyethyl)-aniline, 2-amino-1-propanol~ 3-amino-1-propanol, 2-amino 2-methyl-1 3-propane-diol, 2-amino-2-ethyl-1, 3-propanediol, N-(beta-hydroxy-propyl)-N'-(beta-aminoethyl)-piperazine, tris~hydroxmethyl) amino-methane (also known as trismethylolaminomethane), 2-amino-1-butanol, ethanolamine, beta-(beta-hydroxyethoxy)-ethylamine, and the like. Mixtures of these or similar amines can also be employed.

Preerred dispersants are those derived from polyisobutenyl succinic anhydride and polyethylene amines, e.q. tetraethylene pentamine, polyoxyethylene and polyoxypropylene amines, e.g.
polyoxypropylene diamine, trisrnethylolamino~ethane and pentaerythritol, and combinations thereof. One particularly preferred dispersant combination involves a combination of (A) polyiobutenyl succinic anhydride with (B) a hydroxy compound, e.g. pentaerythritol, (C) a polyoxyalkylene polyamine, e.g.
polyoxypropylene diamine, and (D) a polyalkylene polyamine, e.g. polyethylene diamine and tetraethylene pentamine using about 0.01 to about 4 equivalents of (B) and (D) and about 0~01 to about 2 equivalents of (C) per equivalent of (A) as described in US-A-3894763. Another preferred dispersant combination involves the combination of (A) polyisobutenyl succinic anhydride with (B) a polyalkylene polyamine, e.g~
tetraethylene pentamine, and (C) a polyhydric alcohol or . ,, -,,: '' , 3~6~

polyhydroxy-substituted aliphatic primary amine, e.g.
pentaerythritol or trismethylolaminomethane as described in US-~-3632511.

The alkenyl succinic polyamine type dispersants can be further modified with a boron compound such as boron oxide, boron halides, boron acids and ester of boron acids in an amount to provide 0.1 to 10 atomic proportions of boron per mole of the acylated nitrogen compound as generally taught in US-A-3087936 and 3254025. Mixtures of dispersants can also be used such as those described in US-A-4113639.

The oils may contain from 1.0 to 10 wt %, more preferably 2.0 to 7.0 wt % of these dispersants.

The dispersancy may be provided by 0.3 to 10% of a polymeric Viscosity Index improver dispersant, for example copolymers of alkyl methacrylates with N-vinyl pyrrolidone or dimethylaminoalkyl methacrylate, alkyl fumarate-vinyl acetate N-vinyl pyrolidine copolymers, post-grafted interpolymers of ethylene-propylene with an active monomer such as maleic anhydride which may be further reacted with an alcohol or an alkylene polyamine, such as in US-A-4149984; or styrene/maleic anhydride polymers post-reacted with alcohols and amines, ethoxylated derivatives of acrylate polymers such as in US-A-3702300.

Magnesium and/or calcium containing additives are frequently included in lubricating compositions either alone or in combination with other alkali metal or alkaline earth metal additives such as those containing sodium. These may be present for example as the metal salts of sulphonic acids/
alkyl phenols, sulphurised alkyl phenols, alkyl salicylates, naphthenates, and oGher oil soluble mono- and di-carboxylic acids.

- 12 ~ ~ ~'6~7~

Highly basic alkaline earth metal alkaryl sulfonates are geneeally known for example in US-A-3150088 and 3150089. For the purposes of this invention, a preferred alkaline earth sulfonate is magnesiurn or calcium alkyl aromatic sulfonate having a total base number (TBN, as measured by the procedure of ASTM D2896) ranging from 300 to 400.

Polyvalent metal alkyl salicylate and naphthenate materials may also be included, such as the methylene and sulfur bridged materials which are readily derived from alkyl substituted salicylic or naphthenic acids or mixtures of either or both with alkyl substitu~ed phenols. Basic sulfurized salicylates and a method for their preparation are shown in US-A 3595791.

The sulfurized metal phenates can be considered the ~metal salt of a phenol sulfide~ which thus refers to a metal salt, whether neutral or basic, of a compound typified by the general formula:
b~sx ~ sx ~ 1~

OH OH n OH

where x = 1 or 2, n = 0, 1 or 2 or a polymeric form of such a compound, where R is an alkyl radical, n and x are each integers from 1 to 4, and the average number of carbon atoms in all of the R groups is at least about 9 in order to ensure adequate solubility in oil. The - 13 - ~ ~ ~67~

individual R groups may each contain frorn 5 to 40, preferably 8 to 20, carbon atoms. The metal salt is prepared by reacting an alkyl phenol sulfide with a sufficient quantity o~ metal containing material to impart the desired alkalinity to the sulfurized metal phenate.

The sulfurized alkyl phenol is converted by reaction with a metal containing material including oxides, hydroxides and cornplexes in an amount su~icient to neutralize said phenol and, if desired, to overbase the product to a desired alkalinity by procedures well known in the art. Pre~erred is a process of neutralization utilizing a solution of metal in a glycol ether.

Magnesium and calcium containing additives such as described above although beneficial in other respects can increase the tendency o~ the lubricating oil to oxidise. This is especially true of the highl~ basic sulphonates.

According to a preferred embodiment the invention therefore provides a crankcase lubricating composition also containing ~rom 2 to 8000 parts per million of calcium and/or magnesium.

The magnesium and/or calcium is generally present as basic or neutral detergents such as the sulphonates and phenates, and preferred additives are basic magnesium or calcium sulphonates. Preferably the oils contain from 500 to 5000 parts per million of calcium and/or magnesium ~rom such additives.

These compositions of our invention may as an alternative or in addition contain other similar metal-containing detergent additives, for example, those containing barium, sodium, potassium or lithium.

- 14 - ~3~

The lubricating oil used in the lubricant composition may be a mineral lubricating oil or a synthetic lubricating oil or a mixture thereof. Suitable synthetic oils include diester oils such as di(2-ethyl-hexyl) sebacate, azelate and adipate;
complex ester oils such as those formed for dicarboxylic acids, glycols and either monobasic acids or monohydric alcohols;
silicone oils; sulfide esters; organic carbonates; hydrocarbon oils and other synthetic oils known to the art. The invention is particularly useful in mineral lubricating oils and has the added benefit that it may allow use of base stock oils that have inferior antioxidant properties to those currently used.

The lubricating compositions of the present invention may and usually will contain other traditional lubricant additives provided that they are substantially phosphorus-free - for example, rust inhibitors such as oleic acid and its derivatives, such as N-oleylsarcosine, and oleic acid dimers, and trimers, lecithin~ sorbitan mono-oleate, dodecyl succinic anhydride or ethoxylated alkyl phenols; pour point depressants such as copolymers of vinyl acetate with fumaric acid esters of coconut oil alcohols; and viscosity index improvers such as olefin copolymers or polymethacrylates.

In copper-free oils other antioxidants in addition to the zinc dialkyldithiophosphate are sometimes required to improve the oxidative stability of the oil. These supplementary antioxidants are included especially when the basestock has poor oxidative stability; and typically the supplementary antioxidant is added to the oil in amounts from 0.1-1~5 wt %.
The supplementary antioxidants that are used include phenols, hindered-phenols, bis-phenols, and sulphurised phenols, catechol, alkylated catechols and sulphurised alkyl catechols, diphenylamine and alkyl diphenylamines and phenyl-l-naphthylamine and its alkylated derivatives.

- 15 - ~3~

The inclusion of small amounts of copper generally removes the need for these supplementary antioxidants. It would, however, still be within the scope of our invention for a supplementary antioxldant to be included especially for oils operating under particularly severe conditions where the presence of such supplementary antioxidants may be beneficial, provided that substantially no phosphorus is thereby introduced.

Additives for lubricating oils are generally supplied as concentrates in oil for incorporation into the bulk lubricant.
The present invention therefore provides concentrates comprising an oil solution containing:

(1) less than 0.1 wt % of phosphorus;
~2) from 1 to 50 wt % of an oil-soluble sulphur-containing compound;
(3) from 0.005 to 2 wt % of copper; and (4) from 0.1 to 20 wt % of a bearing corrosion inhibitor, and optionally ~5) a dispersant selected from the group consisting o:

(a) 0 to 6G, e.g. 10 to 60 wt ~ of an ashless dispersant compound, (b) 0 to 40, e.g. 3 to 40~ of a polymeric viscosity index improver dispersant, although it is usual to add any viscosity index improver separately.

The concentrate may also contain other additives such as the deteryents and viscosity index improvers previously described.
A particularly preferred concentrate also contains a magnesium and/or calcium containing additive and the invention therefore provides a concentrate which further comprises from 0.01 to 8 wt ~ of calcium and/or magnesium.

:~3~

The following Examples are now given, though only by way of illustration, to show certain aspects of the invention in more detail.

Comparative Examples I-VI and ~xamples 1 4 In the following Comparative Examples and Examples of the invention, formulations are prepared with the combinations and amounts of additives set out in Table 1, with the balance being a diluent oil suitable for lubricating compositions and comprising 0.3 wt ~ sulphur. The additives used are as follows:

A is a dispersant Y.I. additive comprising an oil solution containing 21% of a multifunctional ethylene-propylene copolymer and containiny 0.29 wt % N.

B is an ashless dispersant comprising a 50 wt % oil solution of borated polyisobutenyl succinimide having a polyisobutenyl radical with a molecular weight of approximately 950 and containing 1.6 wt ~ N and 0.35 wt %
B.

C is an oil solution of an overbased magnesium sulphonate having a TBN of 400 and a magnesium content of 9.2 wt and a sulphur content of 1.7 wt %.

D is an oil solution of an overbased calcium sulphonate having a TBN of 300 and a calcium content of 11.9 wt %
and a sulphur content of 1.9 wt %o ~ is an oil solution of copper oleate containing 4 wt copper.

F is a 30 wt % solution in oil of a hindered methylene bis-phenol antioxidant.

- 17 - ~3~6~

G is an alkylated diphenylamine antioxidant, commercially available as Irganox L-57 fro~ Ciba-Geigy.

H is a 50 wt % oil solution of a zinc diamyl dithiocarbamate containing 6 wt % of zinc and 12 wt %
sulphur.

J is an orthoborate ester made from ethoxyethanol comprising 5 wt ~ of boron.

K is 2,5-bis(nonyldithio)-1,3,4-thiadiazole, co~mercially available as Amoco 158 from Amoco Chemical Company, comprising 33 wt % sulphur.

L is an oil solution containing 12 wt % of molybdenum as the octoate.

M is a sulphurized ester sperm oil substitute, commercially available as Emery 9844 from Emery Corporation, and comprising 11.5 wt % sulphur.

The formulations were tested in the following standard tests:

Seq. IIID engine test according to ASTM STP 315M Part II
in which the maximum and average cam plus lifter wear are measured. A pass in this test is achieved with maximum wear of 0.02 cm tO.008 in.) or better, and an average wear of 0.01 cm (0.004 in.) or better.

Kinematic viscosity increase in the Seq. III~ was measured at 40~C as a percentage increase in 64 hours. A
pass is achieved in this test by achievinq a viscosity increase in 64 hours of not more than 375%.

CRC-L-38 Screener engine test based on ASTM STP 509A PE
IV in which the bearing weight loss (BWL) is measured~ A
pass in this test is achieved with BWL of not more than 40 mg Tf~deinar~

- 18 - ~3~7'~

-The results are shown in Table 2. These results show the invention provides a surprising advantage in lubricants which have excellent antioxidant, anti-wear, and bearing corrosion inhibition with substantial absence of phosphor~s. Comparative Examples I, II and III show that in the absence of a bearing corrosion inhibitor, wear performance was inadequate.
Comparative Example IV shows that the addition ~f a molybdenum additive did not improve wear performance. Comparative Example V shows that in the absence of copper antioxidant performance was inadequate even with conventional amounts of other known antioxidants.

A comparision of Comparative Example V with Example 2 shows that the use of copper not only improves antioxidant performance but also surprisingly improves antiwear performance. The Examples of the invention show that the performance of the formulations is not merely summation of the performance of individual additives, but gives a surprising improvement in antiwear, antioxidant and bearing corrosion performance, while having phosphorus levels below those commercially employed in conventional oils.

~ 3 ~ 6' 7 ~

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a:~ ~ ~ I o I I ~ _t I I I o o o o o o ~ O D ~ ~ U~ ~ O O O ~
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r-l H
.0 O~ ~ ~1 1 0 1 1~1 1 1 0 1 0 0 0 C~ O O

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1~ 0 ~ID ~) O ~ O O 0 ~1 H
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; ~ ~ ~1 1 0 1 1 l l I l I ~ O O O O O

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~ ~: O V
3 ~ aJ v c~ 1:
O V ~ '~
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m ~ o o ~

o ~C ~ ~ O~rl ~ O
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8 g o.
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Comparative Examples VIIX - IX and Examples 5 -_7 A key factor in the performance of crankcase lubricating oils in modern engines is their resistance to oxidation, particularly the avoidance of excessive viscosity increase~ The effectiveness of the compositions of the invention in resisting viscosity increase is demons~rated in the Seq~ IIID engine tests demonstrated in Examples 1-4 above. A further de~onstration is given below in a bench test - the ERCOT test - designed to simulate the oxidative, iron-catalysed environment of an internal combustion engine.

In the ERCOT test reported below a 300 gm sample of the oil composition under test containing 40 ppm of iron as ferric acetylacetonate was oxidised by passing 1.7 l/min o~ air through the sample at 165C and the viscosity was determined at intervals up to 64 hours using a Hakke viscometer. The results are expressed in centipoise (cp).

Comparative Examples VII - IX follow Example 11 oE
WO-A-8604601, Example 13 of WO-A~8604602 and Example XI of WO-A-06092 but using similar materials selected from those identified by letter in these Examples. The Comparative Examples do not use copper, and the results in Table 3 below show inadequate control of viscosity, whereas the compositions of the invention in Examples S-7 de~onstrate the effectiveness of the invention for use in modern oils exposed to an oxidative environment over a long period with extended engine oil drain times.

Apart from the components identified hereinbefore, the following were used:-N is a dispersant similar to dispersant B, but wherein thepolyisobutenyl radical has a molecular weight of approximately 1300, and the dispersant contains 1.46 wt %
N and 0.32 wt ~ B.

P is an anti-wear additive comprising an oil solution (90 active ingredient3 of a diisooctyl 2inc dithiophosphate which contains 7.0 wt % P and 7.7 wt % Zn.

TABLE~ 3 _._ .

Example VII VIII IX 5 6 7 . . ~

Component (%) H 2.0 2.0 - - 1.5 M 2.0 2.0 2.0 1.0 - 1.0 N 4.1 4.1 4.1 4.1 4.1 4.1 C 1.5 1.5 1.5 1.5 1.5 1.5 K 0.1 - - - 0.5 0.5 J - - 2.0 1.0 O . 1 E - - - 0.4 0.4 0.4 Oil To 100% -- ------------------~---------~

- -- - - - _ .. _ _, Visc. (cp) at EIours 38.2 38.9 36.635.6 36.9 3~.9 ~6 95.6 100.~ ~300 38.9 56.1 77.8 24 266.7 293.2 40.8 79.4137.7 ~300 ~300 70.3170.4214.2 4~ 135.818~.9221.6 64 260.8218.4262.4 .

;~3~6~
-~ - 23 -Concentrates - Typical concentrates for providing the above formulations, ~t % %S ~Cu %B

B 33.7 0.12 C1~3 o O i) ~ 31 E 3~4 0~16 J 11.2 . 0.56 M 33~? 3~38 100.0 4.19 0.16 0.68 : Example 4 B 35.7 C 19.1 0.32 0.13 E 3.6 0.14 K 5.9 1.95 M 35.6 4.09 _ 100 6.36 0~14 0~13 Concentrates may also contain some diluent oil to improve handling (reduce viscosity).

Claims (23)

1. A crankcase lubricant composition for use in automobile engines comprising a major amount of a lubricating oil, 5 to 500 parts per million by weight of added copper present in oil-soluble form, one or more added oil-soluble sulphur-containing compounds such that the composition comprises from greater than 0.5 to 2.0 wt.%
of total sulphur and a bearing corrosion inhibiting effective amount of a bearing corrosion inhibitor selected from the group consisting of borate esters, mono-, di- and trihydroxy alkanols, hydroxy esters, oxazolines, sulfur-containing alcohols, amino alcohols and thiadiazole mercaptans and derivatives thereof, the composition containing less than 0.01 wt.% phosphorus, wherein said copper is blended into the oil as an oil-soluble copper compound selected from the group consisting of copper salts of C10 to C18 fatty acids, copper salts of unsaturated carboxylic acids, copper salts of naphthenic acids of molecular weight from 200 to 500, copper salts of alkyl substituted dicarboxylic acids, copper sulphonates, copper phenates, and copper acetylacetonates.
2. A composition as claimed in claim 1, in which the amount of added copper in the composition is from 10 to 200 ppm.
3. A composition as claimed in claim 2, in which the amount of added copper in the composition is from 60 to 200 ppm.
4. A composition as claimed in claim 1, in which the oil-soluble sulphur compound is selected from the group consisting of dithiocarbamates of the formula: (RR'NCSS)n M (wherein R and R' are hydrocarbyl radicals containing 1 to 18 carbon atoms, and n is 1 or 2 and M is a suitable metal), mercaptides, su]phurized unsaturated organic compounds, sulphides, thioethers, thiophenols, thiophenols, thioxanthates, sulphurized esters, thioesters, thioamides, thiazoles and thiadiazoles.
5. A composition as claimed in claim 4, in which the oil-soluble sulphur compound is a dialkyl dithiocarbamate containing 2 to 12 carbon atoms.
6. A composition as claimed in claim l, which contains from greater than 0.5 to 1.0 wt.% total S, including from 0.1 to 0.5 wt.% S as added oil-soluble sulphur-containing compound.
7. A composition as claimed in claim 1, which contains 0.01 to 0.5 wt.% Zn.
8. A composition as claimed in claim 4 which contains from 0.5 to 3 wt.% zinc dithiocarbamate.
9. A composition as claimed in claim 1, in which the bearing corrosion inhibitor is selected from the group consisting of borate eskers of the formulae:

B (OR)3, (RO)2B-O-B(OR)2, (ROBO)3 and (RO)2BO-R1-OB(OR)2 wherein R is a substituted or unsubstituted alkyl, aryl or aralkyl group or two groups R together form a substituted or unsubstituted alkylene group and R1 is a substituted or unsubstituted alkylene group and a thiadiazole polysulphide containing from 5 to 50 carbon atoms, and derivatives and polymers thereof.
10. A composition as claimed in claim 9, which contains from 0.01 to 10 wt.% of a borate ester. 25
11. A composition as claimed in claim 9, in which the borate ester is a tris(ethoxyethyl) orthoborate ester or the biborate of butane-1,3-diol.
12. A composition as claimed in claim 9 which contains from 0.01 to 10 wt.% of 2,5-bis(t-nonyldithio)-1, 3,4-thiadiazole.
13. A composition as claimed in claim 1, which contains less than 0.005 wt.% of phophorus.
14. A composition as claimed in claim 13 which is substantially free of phosphorus.
15. A composition as claimed in claim 1, which further comprises from 1 to 10 wt.% of an ashless dispersant compound.
16. A composition as claimed in claim 1, which further comprises from 0.3 to 10 wt.% of a nitrogen or ester containing polymeric viscosity index improver dispersant.
17. A composition as claimed in claim 1, which comprises from 2 to 8000 parts per million of calcium and/or magnesium.
18. A composition as claimed in claim 17, which comprises from 500 to 5000 parts per million of calcium and/or magnesium as a basic calcium and/or magnesium sulphonate.
19. A composition as claimed in claim 1, which further comprises additives selected from the group consisting of rust inhibitors, pour point depressants, additional anti-oxidants and viscosity index improvers,
20. A concentrate comprising an oil solution containing:
(1) less than 0.1 wt.% of phosphorus;
(2) from 1 to 50 wt.% of an oil-soluble sulphur-containing compound;
(3) from 0.005 to 2 wt.% of copper;
(4) from 0.1 to 20 wt% of a bearing corrosion inhibitor selected from the group consisting of borate esters, mono-, di- and trihydroxy alkanols, hydroxy esters, oxazolines, sulfur-containing alcohols, amino alcohols and thiadiazole mercaptans and derivatives thereof: and (5) from 0 to 60 wt.% of an ashless dispersant, wherein said copper is blended into the oil as an .
oil-soluble copper compound selected from the group consisting of copper salts of C10 to C18 fatty acid , copper salts of unsaturated carboxylic acids, copper salts of naphthenic acids of molecular weight from 200 to 500, copper salts of alkyl substituted dicarboxylic acids, copper salts of alkenyl substituted dicarboxylic acids, copper sulphonates, copper phenates, and copper acetylacetonates.
21. A concentrate as claimed in claim 20, which further comprises from 0.01 to 8 wt.% of calcium and/or magnesium.
22. A method of providing an antioxidant to a phosphorous-free lubricant composition comprising an oil-soluble sulphur-containing compound, a bearing corrosion inhibitor, an ashless dispersant and/or a polymeric viscosity index improver dispersant, and a calcium and/or magnesium containing detergent, in which added copper present in an oil soluble form acts as an antioxidant.
23. A method of formulating a crankcase lubricant composition for automobile engines which contains less than 0.05 wt.% phosphorus in which the combination of 5 to 500 ppm of added copper present in an oil-soluble form, from greater than 0.5 to 2.0 wt.% of total sulphur, and a bearing corrosion inhibitor are used to control oxidation, wear and corrosion and meet at least the quality standard of category SF and/or CD of the API Engine Service Categories, wherein said copper is blended into the oil as an oil-soluble copper compound selected from the group consisting of copper salts of C10 to C18 fatty acids, copper salts of unsaturated carboxylic acids, copper salts of naphthenic acids of molecular weight from 200 to 500, copper salts of alkyl substituted dicarboxylic acids, copper salts of alkenyl substituted dicarboxylic acids, copper sulphonates, copper phenates, and copper acetylacetonates, and wherein said bearing corrosion inhibitor comprises a member selected from the group consisting of borate esters, mono-, di- and trihydroxy alkanols, hydroxy esters, oxazolines, sulfur-containing alcohols and thiadiazole mercaptans and derivatives thereof.
CA000560012A 1987-02-27 1988-02-26 Low phosphorus lubricants Expired - Lifetime CA1306741C (en)

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SG50093G (en) 1993-06-25
MX170110B (en) 1993-09-09
AR244317A1 (en) 1993-10-29
AU603186B2 (en) 1990-11-08
JPS63304096A (en) 1988-12-12
DE3875630T2 (en) 1993-03-18
EP0280580B1 (en) 1992-11-04
EP0280580A3 (en) 1989-07-12
EP0280580A2 (en) 1988-08-31
NO172853C (en) 1993-09-15
DK103788D0 (en) 1988-02-26
KR960014933B1 (en) 1996-10-21
MY103223A (en) 1993-05-29
NO880846L (en) 1988-08-29
BR8800835A (en) 1988-10-04
ES2045102T3 (en) 1994-01-16
ATE82020T1 (en) 1992-11-15
DK103788A (en) 1988-08-28
KR880010106A (en) 1988-10-07
GB8704682D0 (en) 1987-04-01
NO880846D0 (en) 1988-02-26
DE3875630D1 (en) 1992-12-10
ZA881262B (en) 1988-08-22
NO172853B (en) 1993-06-07
JP2505019B2 (en) 1996-06-05
AU1235188A (en) 1988-09-01

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