Patent Grant
11292980
The present invention relates to additive concentrates for use in forming a lubricating oil composition, in particular for use in forming an internal combustion engine lubricating oil composition, especially an automotive internal combustion engine crankcase lubricating oil composition. More specifically, although not exclusively, the present invention relates to such additive concentrates with improved stability; and, to the use of borated dispersants, preferably, in combination with polyalkenyl succinic anhydride(s) as additives in such concentrates to improve the stability of and/or stabilise the additive concentrate.
Lubricating oil compositions for internal combustion engines commonly comprise various combinations of chemical additives designed to impart improved performance characteristics to the lubricant and thereby the engine. The additives are commonly prepared as an additive concentrate comprising a specific combination of additives for a particular application, which are mixed together with diluent oil. The diluent oil facilitates storage and use. To prepare a fully formulated oil, the additive concentrate is mixed with the required base oil(s) and any additional additives.
An additive concentrate can be stored on the shelf for some time between manufacture and use. Given that the additives comprise a variety of different chemicals, it is not unusual for some of the additives to interact with each other. Whilst the chemicals may not necessarily chemically react with one another, some of them do not mix well together. This can result in undesirable generation of haze and/or sediment anchor gel in the additive concentrate.
Additive concentrate stability (i.e. storage stability to mitigate and/or prevent undesirable haze and/or sediment and/or gel in the additive concentrate) is a key concern to additive concentrate formulators. Interaction of additives can limit the combinations of additives that the formulator can use and means that sometimes an additive combination that is desirable for lubricant performance benefits cannot be used due to additive concentrate instability.
It has long been known to use friction modifiers and combinations of friction modifiers to obtain improved performance including improved anti-wear performance and improved fuel economy. However, conventional friction modifiers may cause additive concentrate instability as a result of poor compatibility of the friction modifiers with other additives present in an additive concentrate. This instability typically becomes increasingly pronounced as the amount of these conventional friction modifiers is increased in the additive concentrate. With the current drive to reduce friction coefficients of lubricants in order to improve fuel economy, it is desirable to use higher treat rates of friction modifier. However, this is not generally possible as it results in unacceptable levels of additive concentrate instability.
Known friction modifiers which are used in automotive lubricating oil compositions include ashless nitrogen-free organic friction modifiers which are long chain hydrocarbyl fatty acid esters (i.e. esters formed by the reaction of a long chain fatty acid (e.g. oleic acid), or suitable derivative thereof, and an alkanol (e.g. glycerol)); such friction modifiers include glycerol mono-oleate (GMO). These friction modifiers are typically not only extremely effective in the lubricating oil composition but also are typically relatively inexpensive compared with, for example, nitrogen-containing friction modifiers. It is therefore desirable to use such ashless nitrogen-free organic friction modifiers in lubricating oil compositions, particularly automotive internal combustion engine lubricating oil combustions.
Metal detergents are additives which are typically included in an additive concentrate for use in forming a lubricating oil composition, particularly automotive internal combustion engine lubricating oil combustions. Metal detergents function both as detergents to reduce or remove deposits and as acid neutralizers or rust inhibitors. Salicylate detergents are typically preferred to sulphonate and/or phenate detergents as they confer advantages in terms of piston cleanliness, TBN retention, rust control and anti-oxidancy performance.
Although it has been known that conventional friction modifiers may cause additive concentrate instability (i.e. storage instability due to the interaction of the friction modifier with other additives in the concentrate), particularly when the concentrate includes a relatively large amount of friction modifier, it has now been found that the combination of a particular type of ashless nitrogen-free organic friction modifier, namely a long chain hydrocarbyl fatty acid ester (e.g. glycerol mono-oleate), and a particular type of detergent, namely an alkali or alkaline earth metal salicylate detergent, in an additive concentrate may significantly increase additive concentrate instability (i.e. an increase in storage instability), even when the long chain hydrocarbyl fatty acid ester friction modifier is present in the additive concentrate in a relatively low amount. Consequently, when formulating a lubricating oil composition which includes an alkali or alkaline earth metal salicylate detergent and a long chain hydrocarbyl fatty acid ester friction modifier, particularly such a lubricating oil composition where it is desirable to include a relatively large amount of the friction modifier, the alkali or alkaline earth metal salicylate detergent together with other lubricant additives is typically blended to form an additive concentrate which is then added to an oil of lubricating viscosity (i.e. base stock) and the long chain hydrocarbyl fatty acid ester friction modifier is typically added separately to the lubricating oil composition in the form of a separate package. Accordingly, the present invention aims to solve the aforementioned technical problems of providing a storage stable additive concentrate which includes both an alkali or alkaline earth metal salicylate detergent and an ashless nitrogen-free organic friction modifier which is a long chain hydrocarbyl fatty acid ester, particularly an additive concentrate including such a friction modifier in a relatively large amount. Suitably, the present invention aims to provide such an additive concentrate which exhibits the requisite storage stability, thereby mitigating and/or preventing the formation of haze and/or sediment and/or gelation of the concentrate during storage. Conveniently, such an additive concentrate may permit the formation of a lubricating oil composition containing both an alkali or alkaline earth metal salicylate detergent and an ashless nitrogen-free organic friction modifier which is a long chain hydrocarbyl fatty acid ester, particularly a lubricating oil composition containing a relatively large amount of such a friction modifier, by adding a single additive concentrate to an oil of lubricating viscosity (i.e. base stock).
In accordance with a first aspect, the present invention provides an additive concentrate for use in forming a lubricating oil composition, the additive concentrate consisting of a diluent oil of lubricating viscosity present in a minor amount of less than 50 mass %, based on the total mass of the additive concentrate, and a plurality of oil-soluble or oil-dispersible additives contained therein, wherein the combined amount of all of said plurality of additives in the additive concentrate is greater than 50 mass % oar an active ingredient basis, based on the total mass of the additive concentrate, and wherein the plurality of additives include the following additives:
It will be appreciated that the term “stabilise the additive concentrate” refers to the storage stability of the additive concentrate as evidenced by the formation of any haze and/or sediment and/or gelation of the concentrate during storage. Preferably, the storage stability of the additive concentrate is assessed at 60° C. and atmospheric pressure, more preferably over a 12 week period, especially using the Storage Stability Test Method as described herein. Suitably, improvements in storage stability of the additive concentrate are believed to be due to mitigating and/or reducing interactions between additives (A) and (B) in the concentrate.
In a preferred form of the first aspect, the present invention provides an additive concentrate far use in forming a lubricating oil composition, the additive concentrate consisting of a diluent oil of lubricating viscosity present in a minor amount of less than 50 mass %, based on the total mass of the additive concentrate, and a plurality of oil-soluble or oil-dispersible additives contained therein, wherein the combined amount of all of said plurality of additives in the additive concentrate is greater than 50 mass % on an active ingredient basis, based on the total mass of the additive concentrate, and wherein the plurality of additives include the following additives:
In this preferred aspect, the average succination ratio (SR) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, may be greater than or equal to 1.30, more preferably greater than or equal to 1.35, most preferably greater than or equal to 1.55.
In this preferred aspect, the number average molecular weight (Mn) of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, is greater than or equal to 1000, such as 1250, more preferably greater than or equal to 1300, even more preferably greater than or equal to 1350.
Unexpectedly, it has been found that the inclusion of the one or more borated dispersants (C), preferably in combination with the one or more poly(C2 to C6)alkylenyl succinic anhydrides (D), in an additive concentrate typically stabilise and/or improve the storage stability of the additive concentrate when the additive concentrate includes at least the following additives: (A) an alkali or alkaline earth metal salicylate detergent, as defined herein; and, (B) a friction modifier which is an aliphatic (C7 to C29)hydrocarbyl fatty acid ester, as defined herein.
In particular, it has been found that the use of the one or more borated dispersant(s) (C) typically enhances the storage stability of the additive concentrate when used in combination with relatively low concentration levels of the one or more poly(C2 to C6)alkylenyl succinic anhydrides (D), the two additives providing a combined effect that improves and/or stabilises the storage stability of the additive concentrate to a relatively high degree. Suitably, this permits the detergent and friction modifier to be successfully formulated together in a single additive product. The use of one or more of the preferred embodiments of the poly(C2 to C6)alkylenyl succinic anhydrides (D), as defined herein, typically enables a further reduction in the concentrations of both the succinic anhydride and borated dispersant materials to achieve the desired level of package stability.
Thus, it has been found that by increasing the average succination ratio of the optional, albeit preferred, one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D) typically further stabilises and/or improves the storage stability of such an additive concentrate. Moreover, increasing the number average molecular weight of the poly(C2 to C6)alkylenyl chain(s) of the optional, albeit preferred, poly(C2 to C6)alkylenyl succinic anhydride(s) (D) (e.g. a number average molecular weight of the poly(C2 to C6)alkylenyl chain(s) of greater than or equal to 1250 daltons) typically further stabilises and/or improves the storage stability of such an additive concentrate.
Accordingly, the present invention permits the formulation of a stable additive concentrate (i.e. storage stable additive concentrate) which includes the combination of one or more alkali or alkaline earth metal salicylate detergent(s) (A), as defined herein, and one or more ashless nitrogen-free organic friction modifier(s) which is an aliphatic (C7 to C29)hydrocarbyl fatty acid ester (B), as defined herein, particularly such an additive concentrate including such a friction modifier in a relatively large amount.
Conveniently, the additive concentrate of the present invention may facilitate the formulation of a lubricating oil composition which includes both an alkali or alkaline earth metal salicylate detergent and a friction modifier which is an aliphatic (C7 to C29)hydrocarbyl fatty acid ester, particularly a lubricating oil composition including such a detergent and a relatively large quantity of such an ashless nitrogen-free organic friction modifier, by the addition of a single additive concentrate to an oil of lubricating viscosity (i.e. base stock).
It has been found that by increasing the average succination ratio (SR) of the optional, albeit preferred, one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, typically improves the storage stability of and/or stabilises the additive concentrate. The average succination ratio of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, is preferably greater than or equal to 1.30, preferably greater than or equal to 1.35, such as 1.40, more preferably greater than or equal to 1.45, even more preferably greater than or equal to 1.50, even more preferably greater than or equal to 1.55. Preferably, the average succination ratio of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, is less than or equal to 4.00, more preferably less than or equal to 3.50, even more preferably less than or equal to 3.20, even more preferably less than or equal to 3.00, even more preferably less than or equal to 2.75, even more preferably less than or equal to 2.50. A highly preferred average succination ratio of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) is from 1.35 to 3.50, especially from 1.40 to 3.00, and most especially from 1.50 to 2.75.
Alternatively, or additionally, it has been found that by increasing the number average molecular weight (Mn) of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, typically improves the storage stability of and/or stabilises the additive concentrate. Preferably, the number average molecular weight (Mn) of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s), as defined herein, is greater than or equal to 1000, such as 1250, more preferably greater than or equal to 1300, even more preferably greater than or equal to 1350, even more preferably greater than or equal to 1400, even more preferably greater than or equal to 1450, most preferably greater than or equal to 1500, daltons. Preferably, the number average molecular weight (Mn) of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s), as defined herein, is less than or equal to 5000, more preferably less than or equal to 4500, even more preferably less than or equal to 4000, even more preferably less than or equal to 3500, most preferably less than or equal to 3000, daltons. Highly preferred is where the number average molecular weight of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6 alkylenyl succinic anhydride(s) is from 1700 to 2500 daltons.
Additionally, or alternatively, it has also been found that by increasing the average saponification value (SAP value) of the optional, albeit proffered, one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, improves the storage stability of and/or stabilises the additive concentrate. Preferably, the average SAP value of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, is greater than or equal to 45, more preferably greater than or equal to 50, even more preferably greater than or equal to 55, even more preferably greater than or equal to 60, even more preferably greater than or equal to 65, even more preferably greater than or equal to 70 mg, even more preferably greater than or equal to 75 KOH/g (as measured in accordance with ASTM D94).
Preferably, the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D) is one or more polyisobutylenyl succinic anhydride(s) (PIBSA(s)).
Preferably, the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) (B), as defined herein, represent the only ashless nitrogen-free organic friction modifier(s) included in the additive concentrate. More preferably, the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) (B), as defined herein, represent the only ashless organic friction modifier(s) included in the additive concentrate.
Preferably, the one or more alkali or alkaline earth metal salicylate detergent(s) (A), as defined herein, represent the only metal detergent(s) included in the additive concentrate, more preferably the only detergent(s) (i.e. which includes both ash containing and ashless detergents) included in the additive concentrate.
In accordance with a second aspect, the present invention provides a method of forming a lubricating oil composition, preferably an internal combustion engine lubricating oil composition, comprising mixing the additive concentrate of the first aspect of the present invention with an oil of lubricating viscosity (i.e. base stock). Suitably, the internal combustion engine lubricating oil composition is for use in a spark-ignited or compression-ignited, especially a spark-ignited, internal combustion engine. Suitably, the lubricating oil composition, particularly the internal combustion engine lubricating oil composition, as defined herein, is a crankcase lubricating oil composition, especially an automotive internal combustion engine crankcase lubricating oil composition.
In accordance with a third aspect, the present invention provides the use of one or more borated dispersants (C) as an additive in an effective amount in an additive concentrate to improve the storage stability of the additive concentrate, wherein the additive concentrate consists of a diluent oil of lubricating viscosity present in a minor amount of less than 50 mass % based on the total mass of the additive concentrate, and a plurality of oil-soluble or oil-dispersible additives contained therein, wherein the combined amount of all of said plurality of additives in the additive concentrate is greater than 50 mass % on an active ingredient basis, based on the total mass of the additive concentrate, and wherein the plurality of additives include at least the following additives: (A) one or more oil-soluble or oil-dispersible alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, present in an amount of greater than or equal to 3.0 mass % on an active ingredient basis, based on the total mass of the additive concentrate; and, (B) one or more oil-soluble or oil-dispersible ashless nitrogen-free organic friction modifier(s) which is one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s), as defined herein, present in an amount of greater than or equal to 0.50 mass % on an active ingredient basis, based on the total mass of the additive concentrate.
Suitably, the improvement in storage stability of the additive concentrate is evidenced by mitigating and/or reducing the formation of haze, sediment and/or gelation of the additive concentrate. Preferably, the storage stability of the additive concentrate is assessed at a temperature of 60° C. and atmospheric pressure, more preferably over a 12 week period, especially using the Storage Stability Test Method as described herein.
In a preferred form of the third aspect, the invention provides the use of one or more borated dispersants (C) in combination with one or more oil-soluble or oil-dispersible poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, in an additive concentrate in a combined effective amount to improve the storage stability of the additive concentrate, wherein the additive concentrate consists of a diluent oil of lubricating viscosity present in a minor amount of less than 50 mass %, based on the total mass of the additive concentrate, and a plurality of oil-soluble or oil-dispersible additives contained therein, wherein the combined amount of all of said plurality of additives in the additive concentrate is greater than 50 mass % on an active ingredient basis, based on the total mass of the additive concentrate, and wherein the plurality of additives include at least the following additives: (A) one or more oil-soluble or oil-dispersible alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, present in an amount of greater than or equal to 3.0 mass % on an active ingredient basis, based on the total mass of the additive concentrate; and, (B) one or more oil-soluble or oil-dispersible ashless nitrogen-free organic friction modifier(s) which is one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s), as defined herein, present in an amount of greater than or equal to 0.50 mass % on an active ingredient basis, based on the total mass of the additive concentrate.
In accordance with a fourth aspect, the present invention provides the use of one or more borated dispersants (C), as defined herein, as an additive in an effective amount in an additive concentrate to improve the compatibility of and/or mitigate interaction between and/or prevent interaction between (A) one or more oil-soluble or oil-dispersible alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, as an additive present in an amount of greater than or equal to 3.0 mass % on an active ingredient basis, based on the total mass of the additive concentrate; and, (B) one or more oil-soluble or oil-dispersible ashless nitrogen free organic friction modifier(s) which is one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s), as defined herein, as an additive present in an amount of greater than or equal to 0.50 mass % on an active ingredient basis, based on the total mass of the additive concentrate, and wherein the additive concentrate consists of a diluent oil of lubricating viscosity present in a minor amount of less than 50 mass %, based on the total mass of the additive concentrate, and a plurality of oil-soluble or oil-dispersible additives, including at least additives (A) and (B), contained therein, and the combined amount of all of said plurality of additives in the additive concentrate is greater than 50 mass % on an active ingredient basis, based on the total mass of the additive concentrate.
Suitably, the improvement in compatibility of and/or the mitigation of and/or the prevention of interaction between said (A) one or more oil-soluble or oil-dispersible alkali metal or alkaline earth metal salicylate detergent(s) and said (B) one or more oil-soluble or oil-dispersible ashless nitrogen-free organic friction modifier(s) in the additive concentrate by the use of the one or more borated dispersants (C) is evidenced by mitigating and/or reducing the formation of haze, sediment and/or gelation of the additive concentrate. Preferably, the formation of haze, sediment and/or gelation of the additive concentrate is assessed at a temperature of 60° C. and atmospheric pressure, more preferably over a 12 week period, especially using the Storage Stability Test Method as described herein. Accordingly, the additive concentrate typically exhibits improved storage stability.
In a preferred embodiment of the fourth aspect of the invention, the one or more borated dispersants (C) is used in combination with one or more oil-soluble or oil-dispersible poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, in the additive concentrate in a combined effective amount to improve the compatibility of and/or mitigate interaction between and/or prevent interaction between additives (A) and (B) of the concentrate.
In the preferred use of the third and fourth aspects, the average succination ratio of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D) is preferably greater than or equal to 1.35.
In the preferred use of the third and fourth aspects, the number average molecular weight (Mn) of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D) is preferably greater than or equal to 1250 daltons.
In the preferred use of the third and fourth aspects, the average saponification value (SAP value) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D) is preferably greater than or equal to 45, as measured in accordance with ASTM D94.
The additive concentrate of the first aspect, and as defined in the second to fourth aspects, of the invention may further include, in addition to additives (A), (B), (C) and preferably (D), one or more oil-soluble or oil-dispersible, ashless (non-borated) dispersant(s) (G), preferably one or more oil-soluble or oil-dispersible nitrogen-containing ashless non-borated dispersant(s). Preferably, the one or more oil-soluble or oil-dispersible ashless dispersant(s) (G), as defined herein, is present in an amount of greater than or equal to 5 mass %, more preferably greater than or equal to 10 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the one or more oil-soluble or oil-dispersible ashless dispersant(s) (G), as defined herein, is present in an amount of less than or equal to 50 mass %, more preferably less than or equal to 45 mass %, even more preferably less than or equal to 40 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Although the inclusion of additive (G) in the concentrate is preferred, it is not essential.
The additive concentrate of the first aspect, and as defined in the second to fourth aspects, of the invention may further include, in addition to additives (A), (B) (C) and preferably (D), and optional additive (G) if present, one or more oil-soluble or oil-dispersible dihydrocarbyl dithiophosphate metal salt(s) (E), as defined herein. Preferably, the one or more oil-soluble or oil-dispersible dihydrocarbyl dithiophosphate metal salt(s) (E) is present in an amount of greater than or equal to 2 mass %, more preferably greater than or equal to 3 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the one or more oil-soluble or oil-dispersible dihydrocarbyl dithiophosphate metal salt(s) (E) is present in an amount of less than or equal to 20 mass %, more preferably less than or equal to 15 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Although the inclusion of additive (E) in the concentrate is preferred, it is not essential.
The additive concentrate of the first aspect, and as defined in the second to fourth aspects, of the invention may further include, in addition to additives (A), (B), (C) and preferably (D), and optional additives (U) and/or (E) if present, one or more oil-soluble or oil-dispersible ashless anti-oxidant(s) (F), as defined herein. Preferably, the one or more oil-soluble or oil-dispersible ashless anti-oxidant(s) (F) is an aminic anti-oxidant, particularly an aromatic amine anti-oxidant, a phenolic anti-oxidant or a combination thereof, especially an aromatic amine anti-oxidant. Preferably, the one or more oil-soluble or oil-dispersible ashless anti-oxidant(s) (F), as defined herein, is present in an amount of greater than or equal to 3 mass %, more preferably greater than or equal to 5 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the one or more oil-soluble or oil-dispersible ashless anti-oxidant(s) (F), as defined herein, is present in an amount of less than or equal to 20 mass %, more preferably less than or equal to 15 mass %, on an active ingredient basis, based on the total mass of the additive concentrate, Although the inclusion of additive (F) in the concentrate is preferred, it is not essential.
The additive concentrate of the first aspect, and as defined in the second to fourth aspects, of the invention may further include, in addition to additives (A), (B), (C) and preferably (D), and optional additives (G), (E) and/or (F), if present, one or more oil-soluble or oil-dispersible co-additives in an amount of from 0.1 to 30 mass % on an active ingredient basis, based on the total mass of the additive concentrate, selected from metal detergents, corrosion inhibitors, pour point depressants, anti-wear agents, friction modifiers, demulsifiers, antifoam agents, molybdenum compounds and viscosity modifiers.
A preferred additive concentrate of the first aspect, and as defined in the second to fourth aspects, of the invention includes the following additives:
optionally one or more additives selected from:
A preferred additive concentrate of the first aspect, and as defined in the second to fourth aspects, of the invention includes the following additives:
wherein (C) and (D) are each present in amounts that are effective, in combination, to stabilise the additive concentrate: and, optionally one or more additives selected from:
A more preferred additive concentrate of the first aspect, and as defined in the second to fourth aspects, of the invention includes the following additives:
optionally one or more additives selected from:
In this specification, the following words and expressions, if and when used, have the meanings given below:
Mw in relation to the poly(C2 to C6)alkylenyl chain(s) of the poly(C2 to C6)alkylenyl succinic anhydride(s) may be considered essentially identical to Mw of the appropriate one or more poly(C2 to C6)alkylene(s) used to form the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) by reaction with an appropriate reactant (e.g. maleic anhydride);
All percentages reported are mass % on an active ingredient basis, i.e, without regard to carrier or diluent oil, unless otherwise stated.
Further, it is understood that any upper and lower quantity, range and ratio limits set forth herein may be independently combined. Accordingly, any upper and lower quantity, range and ratio limits set forth herein associated with a particular technical feature of the present invention may be independently combined with any upper and lower quantity, range and ratio limits set forth herein associated with one or more other particular technical feature(s) of the present invention. Furthermore, any particular technical feature of the present invention, and all preferred variants thereof, may be independently combined with any other particular technical feature(s), and all preferred variants thereof.
Also, it will be understood that the preferred features of each aspect of the present invention are regarded as preferred features of every other aspect of the present invention.
The features of the invention relating, where appropriate, to each and all aspects of the invention, are described in more detail as follows:
Diluent Oil
The diluent oil of the additive concentrate of the first aspect of the present invention and the base stock of a lubricating oil composition (sometimes referred to as “base oil”) to which the additive concentrate is added to form the lubricant may be selected from natural (vegetable, animal or mineral) and synthetic lubricating oils and mixtures thereof.
The base stock groups are defined in the American Petroleum Institute (API) publication “Engine Oil Licensing and Certification System”, Industry Services Department, Fourteenth Edition, December 1996, Addendum 1, December 1998.
Definitions for the base stocks and base oils in this invention are the same as those found in the American Petroleum Institute (API) publication “Engine Oil Licensing and Certification System”, Industry Services Department, Fourteenth Edition, December 1996, Addendum 1, December 1998. Said publication categorizes base stocks as follows:
Preparation of the additive concentrate may be accomplished by adding the neat additives directly to the diluent oil or by adding them in a form which includes a carrier oil. Suitably, additives included in the additive concentrate may comprise a carrier oil; any such carrier is considered part of the diluent oil of the additive concentrate of the first aspect of the present invention for calculating the composition of the additive concentrate. Additives may be added to the diluent oil by any method known to those skilled in the art, either before, at the same time as, or after addition of other additives.
Examples of oils of lubricating viscosity which may be used as the diluent oil or the base stock for a lubricating oil composition containing the additive concentrate of the present invention are detailed as follows.
Natural oils include animal and vegetable oils (e.g. castor and lard oil), liquid petroleum oils and hydrorefined, solvent-treated mineral lubricating oils of the paraffinic, naphthenic and mixed paraffinic-naphthenic types. Oils of lubricating viscosity derived from coal or shale are also useful base oils.
Synthetic lubricating oils include hydrocarbon oils such as polymerized and interpolymerized olefins (e.g. polybutylenes, polypropylenes, propylene-isobutylene copolymers, chlorinated polybutylenes, poly(1-hexenes), poly(1-octenes), poly(1-decenes)); alkylbenzenes (e.g. dodecylbenzenes, tetradecylbenzenes, dinonylbenzenes, di(2-ethylhexyl)benzenes); polyphenols (e.g. biphenyls, terphenyls, alkylated polyphenols); and alkylated diphenyl ethers and alkylated diphenyl sulfides and the derivatives, analogues and homologues thereof.
Another suitable class of synthetic lubricating oils comprises the esters of dicarboxylic acids (e.g. phthalic acid, succinic acid, alkyl succinic acids and alkenyl succinic acids, maleic acid, azelaic acid, suberic acid, sebacic acid, fumaric acid, adipic acid, linoleic acid dimer, malonic acid, alkylmalonic acids, alkenyl malonic acids) with a variety of alcohols (e.g. butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl alcohol, ethylene glycol, diethylene glycol monoether, propylene glycol). Specific examples of these esters include dibutyl adipate, di(2-ethylhexyl) sebacate, di-n-hexyl fumarate, dioctyl sebacate, diisooctyl azelate, diisodecyl azelate, dioctyl phthalate, didecyl phthalate, dieicosyl sebacate, the 2-ethylhexyl diester of linoleic acid dirtier, and the complex ester formed by reacting one mole of sebacic acid with two moles of tetraethylene glycol and two moles of 2-ethylhexanoic acid.
Esters useful as synthetic oils also include those made from C5 to C12 monocarboxylic acids and polyols, and polyol ethers such as neopentyl trimethylolpropane, pentaerythritol, dipentaerythritol and tripentaerythritol.
Unrefined, refined and re-refined oils can be used in the additive concentrate of the present invention, or a lubricating oil composition formed therefrom. Unrefined oils are those obtained directly from a natural or synthetic source without further purification treatment. For example, a shale oil obtained directly from retorting operations, petroleum oil obtained directly from distillation or ester oil obtained directly from an esterification process and used without further treatment would be unrefined oil. 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. Many such purification techniques, such as distillation, solvent extraction, acid or base extraction, filtration and percolation are known to those skilled in the art. Re-refitted oils are obtained by processes similar to those used to obtain refined oils applied to refined oils which have been already used in service. Such re-refined oils are also known as reclaimed or reprocessed oils and often are additionally processed by techniques for approval of spent additive and oil breakdown products.
Other examples of base oil are gas-to-liquid (“GTL”) base oils, i.e. the base oil may be an oil derived from Fischer-Tropsch synthesised hydrocarbons made from synthesis gas containing H2 and CO using a Fischer-Tropsch catalyst. These hydrocarbons typically require further processing in order to be useful as a base oil. For example, they may, by methods known in the art, be hydroisomerized; hydrocracked and hydroisomerized; dewaxed; hydroisomerized and dewaxed.
Preferably, the volatility of the oil of lubricating viscosity (e.g. diluent oil or base stock of a lubricating oil composition), as measured by the Noack test (ASTM D5880), is less than or equal to 20%, preferably less than or equal to 16%, preferably less than or equal to 12%, more preferably less than or equal to 10%.
Suitably, the diluent oil of the additive concentrate is present in an amount of less than or equal to 45 mass %, preferably less than or equal to 40 mass %, more preferably less than or equal to 40 mass %, even more preferably less than or equal to 35 mass %, based on the total mass of the additive concentrate. Suitably the diluent oil of the additive concentrate is present in an amount of greater than or equal to 5 mass %, preferably greater than or equal to 10 mass %, more preferably greater than or equal to 15 mass %, even more preferably greater than or equal to 20 mass %, based on the total mass of the additive concentrate.
Accordingly, the plurality of additives in the additive concentrate are present in corresponding amounts, such that the total amount of the diluent oil and the plurality of additives in the additive concentrate equals 100 mass %, based on the total mass of the additive concentrate. Suitably, the plurality of additives in the additive concentrate are present in an amount of greater than or equal to 55, preferably greater than or equal to 60, more preferably greater than or equal to 65, mass % based on the total mass of the additive concentrate. Suitably, the plurality of additives in the additive concentrate are present in an amount of less than or equal to 95, preferably less than or equal to 90, more preferably less than or equal to 85, even more preferably less than or equal to 80, mass % based on the total mass of the additive concentrate.
Suitably, the diluent oil of the additive concentrate comprises a Group I or Group II base stock, especially a Group I base stock. Preferably, the diluent oil includes greater than or equal to 50 mass %, more preferably greater than or equal to 60 mass %, even more preferably greater than or equal to 70 mass %, especially greater than or equal to 75 mass %, of Group I base stock(s), based on the total mass of the diluent oil.
Salicylate Detergent (A)
A detergent is an additive that reduces formation of piston deposits, for example high-temperature varnish and lacquer deposits, in engines; it normally has acid-neutralising properties and is capable of keeping finely-divided solids in suspension. Most detergents are based on “soaps”, that is metal salts of acidic organic compounds. Accordingly, the additive concentrate of the present invention includes an alkali metal or alkaline earth metal salt of salicylic acid as the soap i.e. salicylate soap.
The additive concentrate of the present invention requires the presence of one or more alkali metal or alkaline earth metal salicylate detergent(s) present in an amount the combined amount of all alkali or alkaline metal salicylate detergent(s)) of greater than or equal to 3.0 mass % on an active ingredient basis, based on the total mass of the additive concentrate.
Preferably, the one or more alkali metal or alkaline earth metal salicylate detergent(s) is present in an amount (i.e. the combined amount of all alkali or alkaline metal salicylate detergent(s)) of greater than or equal to 5.0 mass %, more preferably greater than or equal to 7.5 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the one or more alkali metal or alkaline earth metal salicylate detergent(s) is present in an amount (i.e. the combined amount of all alkali or alkaline metal salicylate detergent(s)) of less than or equal to 30 mass %, more preferably less than or equal to 27.5 mass %, even more preferably less than or equal to 25 mass %, even more preferably less than or equal to 22.5 mass %, even more preferably less than or equal to 20 mass %, on an active ingredient basis, based on the total mass of the additive concentrate.
The salicylic acid(s) are typically prepared by carboxylation, for example by the Kolbe-Schmitt process, of phenoxides. Processes for overbasing the salicylic acid(s) and forming the detergents are known to those skilled in the art.
Detergents generally comprise a polar head with a long hydrophobic tail, the polar head comprising the metal salt of the acidic organic compound. The salts may contain a substantially stoichiometric amount of the metal when they are usually described as normal or neutral salts and would typically have a total base number or TBN at 100% active mass (as may be measured by ASTM D2896) of from 0 to 80. Large amounts of a metal base can be included by reaction of an excess of a metal compound, such as an oxide or hydroxide, with an acidic gas such as carbon dioxide. The resulting overbased detergent comprises neutralised detergent as an outer layer of a metal base (e.g. carbonate) micelle. Such overbased detergents may have a TBN at 100% active mass of 150 or greater, and typically of from 200 to 500 or more.
Suitably, the one or more alkali metal or alkali earth metal salicylate detergent(s), as defined herein, may be neutral or overbased. Suitably, the one or more alkali metal or alkali earth metal salicylate detergent(s) has a TBN at 100% active mass of from 0 to 600 (as may be measured by ASTM D2896). Preferably, the one or more alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, is an overbased alkali metal or alkaline earth metal salicylate detergent. Preferably, the one or more overbased alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, has a TBN at 100% active mass (as may be measured by ASTM D2896) of greater than or equal to 150, preferably greater than or equal to 200, more preferably greater than or equal to 250. Preferably, the one or more overbased alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, has a TBN at 100% active mass (as may be measured by ASTM D2896) of less than or equal to 600, preferably less than or equal to 550, more preferably less than or equal to 500. Suitably, the one or more overbased alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, has a TBN at 100% active mass (as may be measured by ASTM D2896) of from 150 to 600, preferably 150 to 500, more preferably 200 to 500.
Preferably, the one or more alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, is one or more alkali metal or alkaline earth metal C8 to C30 alkyl salicylate detergent(s), more preferably one or more alkali metal or alkaline earth metal C10 to C20 alkyl salicylate detergents(s), most preferably one or more alkali metal or alkaline earth metal C14 to C18 alkyl salicylate detergent(s). The alkyl group(s) may be linear or branched and examples of suitable alkyl groups include: octyl; nonyl; decyl; dodecyl; pentadecyl; octadecyl; eicosyl; docosyl; tricosyl; hexacosyl; and, triacontyl. The one or more alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, may also include sulfurized derivatives thereof.
Preferably, the one or more alkali metal or alkaline earth metal salicylate detergent(s), as defined herein, is one or more alkaline earth metal salicylate detergent(s). Calcium and magnesium salicylate detergent(s) are particularly preferred, especially calcium salicylate detergent(s), more especially overbased calcium salicylate detergent(s). Accordingly, the most preferred one or more alkaline earth metal salicylate detergent(s) is one or more overbased calcium salicylate detergent(s).
Suitably, the additive concentrate includes one or more alkaline earth metal salicylate detergent(s), as defined herein, especially one or more calcium salicylate detergent(s), in an amount of greater than or equal to 3.0 mass % on an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the additive concentrate includes one or more alkaline earth metal salicylate detergent(s), as defined herein, especially one or more calcium salicylate detergent(s), in an amount of greater than or equal to 5.0 mass %, more preferably greater than or equal to 7.5 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the additive concentrate includes one or more alkaline earth metal salicylate detergent(s), us defined herein, especially one or more calcium salicylate detergent(s), in an amount of less than or equal to 30 mass %, more preferably less than or equal to 27.5 mass %, even more preferably less than or equal to 25 mass %, even more preferably less than or equal to 22.5 mass %, even more preferably less than or equal to 20 mass %, on an active ingredient basis, based on the total mass of the additive concentrate.
Preferably, the additive concentrate includes one or more alkaline earth metal salicylate detergent(s), as defined herein, especially one or more calcium salicylate detergent(s), in an amount of from 3.0 to 30, more preferably from 5.0 to 25, even more preferably 5.0 to 20, mass % on an active ingredient basis, based on the total mass of the additive concentrate.
Other metal containing detergents may be present in the additive concentrate and include oil-soluble salts of neutral and overbased sulfonates, phenates, sulfurized phenates, thiophosphonates and naphthenates of a metal, particularly the alkali or alkaline earth metals, e.g. sodium, potassium, lithium, calcium and magnesium. The most commonly used metals are calcium and magnesium, which may both be present in detergents used in a lubricant, and mixtures of calcium and/or magnesium with sodium. Detergents may be used in various combinations,
According to a preferred aspect of the present invention, the one or more alkali or alkaline earth metal salicylate detergent(s), as defined herein, represent the only metal containing detergent(s) in the additive concentrate (i.e. the one or more alkali or alkaline earth metal salicylate detergent(s) is the sole metal containing detergent present in the additive concentrate). More preferably, the only detergent(s) in the additive concentrate is one or more alkaline earth metal salicylate detergent(s), as defined herein, even more preferably one or more calcium salicylate detergents(s), especially one or more overbased calcium salicylate detergent(s).
Friction Modifier (B)
The additive concentrate includes one or more oil-soluble or oil-dispersible ashless nitrogen-free organic friction modifier(s) (B) which is one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s), as defined herein, present in an amount of greater than or equal to 0.50 mass % on an active ingredient basis, based on the total mass of the additive concentrate.
Preferably, the one or more oil-soluble or oil-dispersible aliphatic (C7 to C29 hydrocarbyl fatty acid ester(s), as defined herein, is present in an amount of (i.e. the combined amount of all aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s)) greater than or equal to 0.75, more preferably greater than or equal to 1.0, even more preferably greater than or equal to 1.25, even more preferably greater than or equal to 1.50, even more preferably greater than or equal to 1.50, even more preferably greater than or equal to 1.75, even more preferably greater than or equal to 2.0, mass % on an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the one or more oil-soluble or oil-dispersible aliphatic (C7 to C29) hydrocarbyl fatty acid ester(s), as defined herein, is present in an amount of (i.e. the combined amount of all aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s)) less than or equal to 10 mass %, preferably less than or equal to 7.5 mass %, more preferably less than or equal to 5.0 mass %, even more preferably less than or equal to 4.0 mass %, on an active ingredient basis, based on the total mass of the additive concentrate.
Preferably, the one or more oil-soluble or oil-dispersible aliphatic (C7 to C29 hydrocarbyl fatty acid ester(s), as defined herein, is present in an amount of from 1.0 to 10.0, more preferably from 1.0 to 5.0, even more preferably from 1.5 to 4.0, mass % on an active ingredient basis, based on the total mass of the additive concentrate.
The one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s), as defined herein, may be derived by esterifying the corresponding one or more aliphatic (C7 to C29)hydrocarbyl fatty acid(s), and/or a reactive derivative(s) thereof (e.g. anhydride or acid chloride), with an alkanol using routine techniques well known to those skilled in the art. Alternatively, the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) may be obtained in its natural form e.g. as one or more aliphatic (C7 to C29)hydrocarbyl fatty acid glycerol ester(s). Suitably, the term “aliphatic (C7 to C29)hydrocarbyl” of the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s), as defined herein, refers to the total number of carbon atoms in the aliphatic hydrocarbyl chain of the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid(s) (exclusive of the carbonyl carbon atom of such acid(s)) from which the corresponding ester(s) may be derived therefrom.
Suitable aliphatic hydrocarbyl fatty acid(s) from which the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) may be derived and/or obtained in the natural esterified form (i.e. the glycerol ester) include one or more aliphatic (C7 to C29), preferably (C9 to C27), more preferably (C11 to C23), hydrocarbyl fatty acid(s) (i.e. aliphatic (C7 to C29)hydrocarbyl monocarboxylic acid(s)), wherein Cx to Cy designates the total number of carbon atoms in the aliphatic hydrocarbyl chain of the fatty acid, the fatty acid itself due to the presence of the carboxyl carbon atom includes a total of Cx+1 to Cy+1 carbon atoms. Preferably, the total number of carbon atoms in the one or more aliphatic hydrocarbyl fatty acid(s), inclusive of the carboxyl carbon atom, is an even number. Suitably, the aliphatic hydrocarbyl chain of the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid(s) may be saturated or unsaturated (i.e. including at least one carbon to carbon double bond); preferably, the aliphatic hydrocarbyl chain of the one or more aliphatic (C7 to C29) hydrocarbyl fatty acid(s) is unsaturated and includes at least one carbon to carbon double bond. Preferred one or more aliphatic (C7 to C29)hydrocarbyl fatty acid(s) include one or more of myristoleic acid, palmitoleic acid, sapienic acid, hexadecatrienoic acid, oleic acid, stearidonic acid, elaidic acid, vaccenic acid, linoleic acid, linoelaidic acid, linolenic acid, arachidonic acid, eicosapentaenoic acid, eicosenoic acid, erucic acid, docosahexaenoic acid, docosahexaenoic acid, tetracosapentaenoic acid and tetracosatetraenoic acid. More preferred one or more aliphatic (C7 to C29)hydrocarbyl fatty acids) include one or more of oleic acid, linoleic acid and linolenic acid. Oleic acid is especially preferred.
The one or more aliphatic (C7 to C29)hydrocarbyl fatty acid(s), as defined therein, or a reactive derivative(s) thereof, may be esterified by reaction with one or more alkanol(s), as defined herein, to form the corresponding one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s). Suitable one or more alkanol(s) include monohydric to (C1 to C20) alkanol(s), polyhydric (C2 to C20) alkanol(s), and combinations thereof. Preferably, the one or more alkanol(s) is a polyhydric (C2 to C20) alkanol(s), more preferably a polyhydric (C2 to C15) alkanol(s). Highly preferred polyhydric (C2 to C20) alkanol(s) include glycerol, neopentyl glycol, trimethylolethane, trimethylolpropane, trimethylolbutane, pentaerythritol, dipentaerythritol, tripentaerythritol and sorbitol. Glycerol is especially preferred.
Suitably, preferred one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) include one or more aliphatic (C9 to C27), more preferably (C11 to C23), hydrocarbyl fatty acid ester(s) which may be derived from the corresponding one or more aliphatic (C7 to C29)hydrocarbyl fatty acid(s), as defined herein, by reaction with one or more alkanol(s), as defined herein, or which may be obtained in a natural esterified form i.e. aliphatic (C7 to C29)hydrocarbyl fatty acid glycerol ester(s). Highly preferred one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) include one or more aliphatic (C7 to C29), preferably (C9 to C27), more preferably (C11 to C23), hydrocarbyl fatty acid glycerol ester(s).
The most preferred one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) is glycerol mono-oleate.
According to a preferred embodiment, the additive concentrate includes glycerol mono-oleate in an amount of greater than or equal to 0.50, preferably greater than or equal to 0.75, more preferably greater than or equal to 1.0, even more preferably greater than or equal to 1.25, even more preferably greater than or equal to 1.50, even more preferably greater than or equal to 1.50, even more preferably greater than or equal to 1.75, even more preferably greater than or equal to 2.0, mass % on an active ingredient basis, based on the total mass of the additive concentrate. According to a preferred embodiment, the additive concentrate includes glycerol mono-oleate in an amount of less than or equal to 10, preferably less than or equal to 7.5, more preferably less than or equal to 5.0, even more preferably less than or equal to 4.0, mass % an active ingredient basis, based on the total mass of the additive concentrate.
Preferably, the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) (B), as defined herein, represent the only ashless nitrogen-free organic friction modifier(s) included in the additive concentrate. More preferably, the one or more aliphatic (C7 to C29)hydrocarbyl fatty acid ester(s) (B), as defined herein, represent the only ashless organic friction modifier(s) included in the additive concentrate. Suitably, in a most preferred embodiment, glycerol mono-oleate is the only ashless nitrogen-free organic friction modifier, more preferably the only ashless friction modifier, present in the additive concentrate,
Borated Dispersant (C)
The borated dispersant (C) is prepared by borating the ashless dispersants described below, using known borating means and techniques,
Ashless dispersants are non-metallic organic materials that form substantially no ash on combustion, in contrast to metal-containing, and hence ash-forming, materials. They comprise a long chain hydrocarbon with a polar head, the polarity being derived from inclusion of, e.g. an O, P or N atom. The hydrocarbon is an oleophilic group that confers oil-solubility, having, for example 40 to 500 carbon atoms. Thus, ashless dispersants may comprise an oil-soluble polymeric hydrocarbon backbone having functional groups that are capable of associating with particles to be dispersed. Typically, dispersants comprise amine, alcohol, amide, or ester polar moieties attached to the polymer backbone often via a bridging group. Ashless dispersants may be, for example, selected from oil-soluble salts, esters, amino-esters, amides, imides, and oxazolines of long chain hydrocarbon-substituted mono- and dicarboxylic acids or their anhydrides; thiocarboxylate derivatives of a long chain of hydrocarbons; long chain aliphatic hydrocarbons having a polyamine attached directly thereto, and Mannich condensation products formed by condensing a long chain substituted phenol with formaldehyde and alkylene polyamine, such as described in U.S. Pat. No. 3,442,805.
The oil-soluble polymeric hydrocarbon backbone is typically an olefin polymer or polyene, especially a polymer comprising a major molar amount (i.e. greater than 50 mole %) of a C2 to C18 olefin (e.g. ethylene, propylene, butylenes, isobutylene, pentene, octane-1, styrene), and typically a C2 to C5 olefin. The oil-soluble polymeric hydrocarbon backbone may be homopolymeric (e.g. comprising a copolymer of ethylene and an alpha-olefin such as propylene or butylenes, or a copolymer of two different alpha-olefins).
A preferred class of olefin polymers comprises polybutenes, specifically polyisobutenes (PIB) or poly-n-butenes, such as may be prepared by polymerization of a C4 refinery stream. Other classes of olefin polymers include ethylene alpha-olefin (EAO) copolymers and alpha-olefin homo- and copolymers.
Ashless dispersants include, for example, derivatives of long chain hydrocarbon-substituted carboxylic acids, examples being derivatives of high molecular weight hydrocarbyl-substituted succinic acid. A noteworthy group of dispersants are hydrocarbon-substituted succinimides, made, for example, by reacting the above acids (or derivatives) with a nitrogen-containing compound, advantageously a polyalkylene polyamine, such as polyethylene polyamine. Particularly preferred are the reaction products of polyalkylene polyamines with alkenyl succinic anhydrides, such as described in U.S. Pat. Nos. 3,202,678; 3,154,560; 3,172,892; 3,024,195, 3,024,237; 3,219,666; and 3,216,936; and BE-A-66,875.
Preferred dispersants are polyalkene-substituted succinimides wherein the polyalkene group has a number-average molecular weight in the range of 900 to 5,000. The number-average molecular weight is measured by gel permeation chromatography (GPC). The polyalkene group may comprise a major molar amount (i.e. greater than 50 mole %) of a C2 to C18 alkene, e.g. ethene, propene, butene, isobutene, pentene, octane-1 and styrene. Preferably, the alkene is a C2 to C5 alkene; more preferably it is butene or isobutene, such as may be prepared by polymerisation of a C4 refinery stream. Most preferably, the number average molecular weight of the polyalkene group is in the range of 950 to 2,800.
The above ashless dispersants are post-treated with boron to form the borated dispersant (C), in ways known in the art, such as described in U.S. Pat. Nos. 3,087,936, 3,254,025 and 5,430,105. Boration may for example be accomplished by treating an acyl nitrogen-containing dispersant with a boron compound selected from boron oxide, boron halides, boron acids and esters of boron acids, in an amount sufficient to provide from about 0.1 to about 20 atomic proportions of boron for each mole of ashless dispersant.
The amount of berated dispersant used will vary depending upon the amount of stabilisation required in the circumstances, as typically determined by testing using the Storage Stability Test Method described hereinafter. In general, the amount need only be that which is effective to bring about the required stabilisation of the additive concentrate.
Typically, however, the amount of berated dispersant, as active ingredient, will range from 0.01 to 3 wt %, or more such as up to 4 wt %, preferably from 0.1 to 3.0 wt %, preferably 0.5 to 3.0 wt %, more preferably 0.7 to 2.5 wt %. This range is particularly advantageous for borated polyalkene-substituted succinimides, wherein the polyalkene group preferably has a number-average molecular weight in the range of 900 to 5,000, and more especially the most preferred dispersant defined above.
In embodiments, the one or more borated dispersants (C) is a borated form of an ashless dispersant selected from the oil-soluble salts, esters, amino-esters, amides, imides, and oxazolines of long chain hydrocarbon-substituted mono- and dicarboxylic acids or their anhydrides, thiocarboxylate derivatives of a long chain of hydrocarbons, long chain aliphatic hydrocarbons having a polyamine attached directly thereto, and Mannich condensation products formed by condensing a long chain substituted phenol with formaldehyde and alkylene polyamine.
In embodiments, the one or more borated dispersants (C) is a borated polyalkene-substituted succinimide, wherein the polyalkene group(s) have a number-average molecular weight in the range of 900 to 5,000 as measured by gel permeation chromatography (GPC).
Succinic Anhydride Derivative (D)
The additive concentrate includes one or more oil-soluble or oil-dispersible poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, present in an effective amount (i.e. the combination of all poly(C2 to C6)alkylenyl succinic anhydride(s)) to stabilise the additive concentrate (i.e. to stabilise the additive concentrate as measured in accordance with the storage stability test as described herein).
Preferably, the one or more oil-soluble or oil-dispersible poly(C2 to C6)alkylenyl succinic anhydride(s), as defined herein, is present in an amount of (i.e. the combination of all poly(C2 to C6)alkylenyl succinic anhydride(s)) greater than or equal to 0.75, more preferably greater than or equal to 1.0, even more preferably greater than or equal to 1.25, even more preferably greater than or equal to 1.50, even more preferably greater than or equal to 1.75, even more preferably greater than or equal to 2.0, mass % n an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the one or more oil-soluble or oil-dispersible poly(C2 to C6)alkylenyl succinic anhydride(s), as defined herein, is present in an amount of (i.e. the combination of all poly(C2 to C6)alkylenyl succinic anhydride(s)) less than or equal to 10, more preferably less than or equal to 7.5, even more preferably less than or equal to 5, mass % on an active ingredient basis, based on the total mass of the additive concentrate.
Preferably, the one or more oil-soluble or oil-dispersible poly(C2 to C6)alkylenyl succinic anhydride(s), as defined herein, is present in a total amount of from 1.0 to 10, more preferably from 1.5 to 7.5, even more preferably from 2.0 to 7.5, mass % on an active ingredient basis, based on the total mass of the additive concentrate. In practice, the amount needed to stabilise the additive concentrate in use in combination with the borated dispersant (C) can be determined by using the Storage Stability Test Method described in the examples.
It has been found that by increasing the average succination ratio (SR) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, typically improves the storage stability of and/or stabilises the additive concentrate. The average succination ratio of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, is preferably greater than or equal to 1.30, such as 1.35, more preferably greater than or equal to 1.40, even more preferably greater than or equal to 1.45, even more preferably greater than or equal to 1.50, even more preferably greater than or equal to 1.55. Preferably, the average succination ratio of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (D), as defined herein, is less than or equal to 4.00, more preferably less than or equal to 3.50, even mom preferably less than or equal to 3.20, even more preferably less than or equal to 3.00, even more preferably less than or equal to 2.75, even more preferably less than or equal to 2.50. A highly preferred average succination ratio of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) is from 1.35 to 3.50, especially from 1.40 to 100.
Preferably, the number average molecular weight of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s), as defined herein, is greater than or equal to 1000, preferably greater than or equal to 1250, more preferably greater than or equal to 1300, even more preferably greater than or equal to 1350, even more preferably greater than or equal to 1400, even more preferably greater than or equal to 1450, most preferably greater than or equal to 1500, daltons. Preferably, the number average molecular weight of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s), as defined herein, is less than or equal to 5000, more preferably less than or equal to 4500, even more preferably less than or equal to 4000, even more preferably less than or equal to 3500, most preferably less than or equal to 3000, daltons. Highly preferred is where the number average molecular weight of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) is from 1700 to 3000 daltons.
The number average molecular weight of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) may be considered to be essentially identical to the number average molecular weight (Mn) of the appropriate one or more poly(C2 to C6)alkylene(s) used to form the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (e.g. by reaction with an appropriate reactant, such as maleic anhydride).
Preferably, the ratio of the weight average molecular weight (Mw) to number average molecular weight (Mn), i.e. Mw/Mn, of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) is from 1.5 to 4.0.
Additionally, by increasing the average saponification value (SAP value) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (C), as defined herein, may improve the stability of and/or stabilises the additive concentrate. Preferably, the average SAP value of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) (C), as defined herein, is greater than or equal to 45, more preferably greater than or equal to 50, even more preferably greater than or equal to 55, even more preferably greater than or equal to 60, even more preferably greater than or equal to 65, even more preferably greater than or equal to 70 mg, even more preferably greater than or equal to 75 KOH/g (as measured in accordance with ASTM D94).
Preferably, the one or more poly(C2 to C6)alkylenyl succinic anhydride(s), as defined herein, includes one or more poly(ethylenyl) succinic anhydride(s), poly(propylenyl) succinic anhydride(s), poly(butylenyl) succinic anhydride(s), poly(isobutylenyl) succinic anhydride(s) or combinations thereof. More preferably, the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) comprises one or more poly(C4)alkylenyl succinic anhydrides, even more preferably one or more poly(butylenyl) or poly(isobutylenyl) succinic anhydride(s), especially one or more poly(isobutylenyl) succinic anhydride(s).
In a highly preferred embodiment, the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) is one or more poly(isobutylenyl) succinic anhydride(s) (PIBSA(s)). Said one or more poly(isobutylenyl) succinic anhydride(s) may represent the only one or more poly(C2 to C6)alkylenyl succinic anhydride(s) included in the additive concentrate.
Preferably, the additive concentrate includes one or more PIBSA(s) in an amount of greater than or equal to 0.75, more preferably greater than or equal to 1.0, even more preferably greater than or equal to 1.25, even more preferably greater than or equal to 1.50, even more preferably greater than or equal to 1.75, even more preferably greater than or equal to 2.0, mass % on an active ingredient basis, based on the total mass of the additive concentrate. Preferably, the additive concentrate includes one or more PIBSA(s) in an amount of less than or equal to 10, more preferably less than or equal to 7.5, even more preferably less than or equal to 5, mass % on an active ingredient basis, based on the total mass of the additive concentrate.
Preferably, the one or more PIBSA(s) is present in an amount of from 1.0 to 6.0, more preferably from 1.5 to 5.5, even more preferably from 2.0 to 5.0, mass % on an active ingredient basis, based on the total mass of the additive concentrate.
The one or more poly(C2 to C6)alkylenyl succinic anhydride(s) may be prepared by routine techniques well known to those skilled in the art, for example as disclosed in U.S. Pat. No. 4,234,435. For example, polyisobutylene (PIB) is readily available by cationic polymerization from butene streams (e.g. using aluminium tri-chloride or boron tri-fluoride catalysts). Such polyisobutylenes generally contain residual unsaturation in amounts of about one ethylenic double bond per polymer chain, positioned along the chain. In certain embodiments, the polyisobutylene comprises a highly reactive polyisobutylene (HR-PIB), having a terminal vinylidene content of at least 65%, preferably at least 85%. The preparation of such polymers is described, for example, in U.S. Pat. No. 4,152,499. HR-PIB is known and is commercially available under the tradenames Glissopal (BASF) and Ultravis (BP). Functionalisation of the polyalkylene (e.g. PIB) may be achieved by reaction with maleic anhydride or maleic acid using halogen assisted functionalization or the thermal “ene” reaction, to form the appropriate polyalkenyl succinic anhydride (e.g. PIBSA).
The number average molecular weight (Mn) of the poly(C2 to C6)alkylenyl chain(s) of the one or more poly(C2 to C6)alkylenyl succinic anhydride(s) may be controlled/selected by use of the appropriate precursor poly(C2 to C6)alkylene(s) starting material having the desired number average molecular weight. The average SAP value of the one or more poly(C2 to C6)alkylene succinic anhydride(s) and the average succination ratio of the one or more poly(C2 to C6)alkylene succinic anhydride(s) may be controlled by varying the concentrations of reactants (i.e. varying the concentration of poly(C2 to C6)alkylene(s) and succinic acylating forming group, e.g. maleic anhydride, to form the poly(C2 to C6)alkylenyl succinic anhydride(s).
Dihydrocarbyl Dithiophosphate Metal Salt (E)
The additive concentrate may optionally include one or more oil-soluble or oil-dispersible dihydrocarbyl dithiophosphate metal salt(s) (E), especially one or more dihydrocarbyl dithiophosphate zinc salt(s) (ZDDP(s)).
The preferred one or more zinc dihydrocarbyl dithiophosphate(s) (ZDDP(s)) are oil-soluble salts of dihydrocarbyl dithiophosphoric acids and may be represented by the following formula:
wherein R and R′ may be the same or different hydrocarbyl radicals containing from 1 to 18, preferably 2 to 12, carbon atoms and including radicals such as alkyl, alkenyl, aryl, arylalkyl, alkaryl and cycloaliphatic radicals. Particularly preferred as R and R′ groups are alkyl groups of 2 to 8 carbon atoms. Thus, the radicals may, for example, be ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, amyl, n-hexyl, i-hexyl, n-cetyl, decyl, dodecyl, octadecyl, 2-ethylhexyl, phenyl, butylphenyl, cyclohexyl, methylcyclopentyl, propenyl, butenyl. In order to obtain oil solubility, the total number of carbon atoms (i.e. R and R′) in the dithiophosphoric acid will generally be about 5 or greater. The one or more zinc dihydrocarbyl dithiophosphate(s) can therefore comprise one or more zinc diallyl dithiophosphate(s).
Suitably, if present, the one or more dihydrocarbyl dithiophosphate metal salt(s) (E), especially one or more dihydrocarbyl dithiophosphate zinc salt(s) (ZDDP(s)), as defined herein, is present in an amount of greater than or equal to 2 mass %, more preferably greater than or equal to 3 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Suitably, if present, the one or more dihydrocarbyl dithiophosphate metal salt(s) (E), especially one or more dihydrocarbyl dithiophosphate zinc salt(s) (ZDDP(s)), as defined herein, is present in an amount of less than or equal to 20 mass %, more preferably less than or equal to 15 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Although the inclusion of additive (E) in the concentrate is preferred, it is not essential.
Anti-Oxidant (F)
The additive concentrate may optionally include one or more oil-soluble or oil-dispersible ashless anti-oxidant(s) (F).
Suitably, the one or more oil-soluble or oil-dispersible ashless anti-oxidant(s) (F) is an aminic anti-oxidant(s), particularly an aromatic amine anti-oxidant, a phenolic anti-oxidant(s) or a combination thereof, especially an aromatic amine anti-oxidant(s) such as a dialkyl substituted diphenylamine(s).
Suitably, if present, the one or more oil-soluble or oil-dispersible ashless anti-oxidant(s) (F), as defined herein, is present in an amount of greater than or equal to 3 mass %, more preferably greater than or equal to 5 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Suitably, if present, the one or more oil-soluble or oil-dispersible ashless anti-oxidant(s) (F), as defined herein, is present in an amount of less than or equal to 20 mass %, more preferably less than or equal to 15 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Although the inclusion of additive (F) in the concentrate is preferred, it is not essential.
Non-Borated Ashless Dispersant (G)
The additive concentrate may optionally include one or more oil-soluble or oil-dispersible non-borated ashless dispersant(s) (G), preferably one or more oil-soluble or oil-dispersible non-borated ashless nitrogen-containing dispersant(s).
Non-borated ashless dispersants comprise an oil-soluble polymeric hydrocarbon backbone having functional groups that are capable of associating with particles to be dispersed. Typically, the dispersants comprise amine, alcohol, amide, or ester polar moieties attached to the polymer backbone often via a bridging group. The ashless dispersants may be, for example, selected from oil-soluble salts, esters, amino-esters, amides, imides, and oxazolines of long chain hydrocarbon substituted mono and dicarboxylic acids or their anhydrides; thiocarboxylate derivatives of long chain hydrocarbons; long chain aliphatic hydrocarbons having a polyamine attached directly thereto; and Mannich condensation products formed by condensing a long chain substituted phenol with formaldehyde and a polyalkylene polyamine.
Highly preferred non-borate ashless dispersant(s) (G), if present, include one or more polyalkylene succinimide(s), especially one or more polyisobutylene succinimide(s) (PIBSA-PAM). Such dispersant(s) are typically formed by reaction of the corresponding polyalkylene succinic anhydride (e.g. PIBSA) with a polyamine (PAM). If one or more ashless(s) dispersant(s), is present, then preferably the one or more polyalkylene succinimide(s), especially one or more polyisobutylene succinimide(s), represent the only ashless containing dispersants in the additive concentrate.
Suitably, if present, the one or more ashless dispersant(s) (G), as defined herein, especially the one or more polyalkylene succinimide(s) (e.g. PIBSA-PAM), is present in an amount of greater than or equal to 5 mass %, more preferably greater than or equal to 10 mass %, even more preferably greater than equal to 15 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Suitably, if present, the one or more ashless dispersant(s) (G), as defined herein, especially the one or more polyalkylene succinimide(s) (e.g. PIBSA-PAM), is present in an amount of less than or equal to 50 mass %, more preferably less than or equal to 45 mass %, even more preferably less than or equal to 40 mass %, on an active ingredient basis, based on the total mass of the additive concentrate. Although the inclusion of additive (G) in the concentrate is preferred, it is not essential.
Co-Additives
Other co-additives, in addition to additives (A), (B), (C), and preferably (D) (and the optional additives (F), (F) and (G) if present) which may be included in the additive concentrate of the present invention, or a lubricating oil compositions derived therefrom, comprise one or more oil-soluble or oil-dispersible co-additives selected from metal-containing detergents, corrosion inhibitors, pour point depressants, anti-wear agents, friction modifiers, anti-foam agents, viscosity modifiers, demulsifiers, and oil-soluble molybdenum compounds. Suitably, such co-additive(s) (i.e. the total amount of all such co-additives) are present in an amount of 0.1 to 30 mass %, on an active ingredient basis, based on the total mass of the additive concentrate.
Metal detergents that may be used include oil-soluble neutral and overbased sulfonates, phenates, sulfurized phenates, thiophosphonates, naphthenates and other oil-soluble carboxylates of a metal, particularly the alkali or alkaline earth metals, e.g., sodium, potassium, lithium, calcium, and magnesium. The most commonly used metals are calcium and magnesium, which may both be present in detergents, and mixtures of calcium and/or magnesium with sodium. Combinations of detergents, whether overbased or neutral or both, may be used.
Ashless anti-wear agents may be used and include 1, 2, 3-triazoles, benzotriazoles, sulfurized fatty acid esters and dithiocarbamate derivatives.
The concentrate may also include one or more oil-soluble or sail-dispersible molybdenum compound(s), which include dithiocarbamates, dithiophosphates, dithiophosphinates, xanthates, thioxanthates, sulfides, and the like, and mixtures thereof. Particularly preferred are molybdenum dithiocarbamates, dialkyldithiophosphates, alkyl xanthates and alkylthioxanthates.
Suitable molybdenum compounds include mono-, di-, tri- or tetra-nuclear. Dinuclear and trinuclear molybdenum compounds are preferred, especially preferred are trinuclear molybdenum compounds. Suitable molybdenum compounds are preferably organo-molybdenum compound. More preferably, any molybdenum compound is selected from the group consisting of molybdenum dithiocarbamates (MoDTC), molybdenum dithiophosphates, molybdenum dithiophosphinates, molybdenum xanthates, molybdenum thioxanthates, molybdenum sulfides and mixtures thereof. Most preferably, any molybdenum compound is present as a molybdenum dithiocarbamate compound.
Viscosity modifiers (VM) function to impart high and low temperature operability to a lubricating oil. The VM used may have that sole function, or may be multifunctional. Multifunctional viscosity modifiers that also function as dispersants are also known. Suitable viscosity modifier are polyisobutylene, copolymers of ethylene and propylene and higher alpha-olefins, polymethacrylates, polyalkylmethacrylates, methacrylate copolymers, copolymers of an unsaturated dicarboxylic acid and a vinyl compound, inter polymers of styrene and acrylic esters, and partially hydrogenated copolymers of styrene/isoprene, styrene/butadiene, and isoprene/butadiene, as well as the partially hydrogenated homopolymers of butadiene and isoprene and isoprene/divinylbenzene.
Rust inhibitors selected from the group consisting of nonionic polyoxyalkylene polyols and esters thereof, polyoxyalkylene phenols, and anionic alkyl sulfonic acids may be used.
Copper and lead bearing corrosion inhibitors may be used, but are typically not required with the formulation of the present invention. Typically such compounds are the thiadiazole polysulfides containing from 5 to 50 carbon atoms, their derivatives and polymers thereof. Other additives are the thio and polythio sulfenamides of thiadiazoles and benzotriazoles derivatives.
A small amount of a demulsifying component may be used. A preferred demulsifying component is described in EP 330,522. It is obtained by reacting an alkylene oxide with an adduct obtained by reacting a bis-epoxide with a polyhydric alcohol.
Pour point depressants, otherwise known as lube oil flow improvers, lower the minimum temperature at which the fluid will flow or can be poured. Such additives are well known. Typical of those additives which improve the low temperature fluidity of the fluid are C8 to C18 dialkyl fumarate/vinyl acetate copolymers, polyalkylmethacrylates and the like.
Foam control can be provided by many compounds including an antifoamant of the polysiloxane type, for example, silicone oil or polydimethyl siloxane.
The individual additive(s) may be incorporated into the diluent oil in any convenient way. Preferably, all the additives except for the viscosity modifier and the pour point depressant are blended into the additive concentrate, and that additive concentrate is subsequently blended into base stock to make a finished lubricant. The additive concentrate will typically be formulated to contain the additive(s) in proper amounts to provide the desired concentration in a fully formulated lubricant when the concentrate is combined with a predetermined amount of a base stock.
The concentrate may be made in accordance with the method described in U.S. Pat. No. 4,938,880. That patent describes making a pre-mix of ashless dispersant and metal detergents that is pre-blended at a temperature of at least about 100° C. Thereafter, the pre-mix is cooled to at least 85° C. and the additional components are added.
Typically, 2 to 20, preferably 4 to 18, and most preferably 5 to 17, mass % of the additive concentrate is mixed with a corresponding amount of base stock (i.e. the balance of 100 mass %) when formulating a lubricating oil composition.
Typically, the additive concentrate of the present invention suitably contains up to 4, more preferably up to 3, most preferably up to 2, mass % sulphur, based on the total mass of the concentrate and as measured according to ASTM method D4927.
Typically, a lubricating oil composition prepared from the additive concentrate of the present invention suitably contains up to 0.4, more preferably up to 0.3, most preferably up to 0.2, mass % sulphur, based on the total mass of the composition and as measured according to ASTM method D4927.
The additive concentrate of the present invention suitably contains up to and including 12 mass %, preferably up to 10 mass %, even more preferably up to 9 mass % sulphated ash as measured by ASTM D874.
Typically, a lubricating oil composition prepared from the additive concentrate of the present invention suitably contains up to and including 1.2 mass %, preferably up to 1.1 mass %, even more preferably up to 1.0 mass % sulphated ash as measured by ASTM D874.
Typically, the additive concentrate of the present invention suitably contains up to 2.0 more preferably up to 1.5, even more preferably up to 1.0, mass % nitrogen, based on the total mass of the concentrate and as measured according to ASTM method D5291.
Typically, a lubricating oil composition prepared from the additive concentrate of the present invention suitably contains up to 0.30, more preferably up to 0.20, even more preferably up to 0.15, mass % nitrogen, based on the total mass of the composition and as measured according ASTM method D5291.
Typically, a lubricating oil composition prepared from the additive concentrate of the present invention suitably contains up to and including 1200 ppm, preferably up to and including 1000 ppm, more preferably up to and including 800 ppm, of phosphorus as measured according to ASTM D5185.
Typically, the additive concentrate of the present invention has a total base number (TBN) as measured by ASTM D2896 of from 25 to 100, preferably from 45 to 80.
Typically, a lubricating oil composition prepared from the additive concentrate of the present invention suitably has a total base number (TBN) as measured by ASTM D2896 of from 4 to 15, preferably from 5 to 12.
Preferably, a lubricating oil composition prepared from the additive concentrate of the present invention is a multigrade identified by the viscometric descriptor SAE 20WX, SAE 15WX, SAE 10WX, SAE 5WX or SAE 0WX, where X represents any one of 20, 30, 40 and 50; the characteristics of the different viscometric grades can be found in the SAE J300 classification. More preferably, the lubricating oil composition is in the form of an SAE 10WX, SAE 5WX or SAE 0WX, preferably in the form of an SAE 5WX or SAE 0WX, wherein X represents any one of 20, 30, 40 and 50, especially where X is 20 or 30.
Suitably, the additive concentrate of the present invention is used to form a lubricating oil composition that is used to lubricate mechanical engine components, particularly in internal combustion engines, e.g. spark-ignited or compression-ignited internal combustion engines. Preferably, the additive concentrate of the present invention is used to form a spark-ignited or compression-ignited internal combustion engine lubricating oil composition, more preferably a spark-ignited or compression-ignited internal combustion engine crankcase lubricating oil composition, even more preferably an automotive spark-ignited or compression-ignited internal combustion engine crankcase lubricating oil composition.
The invention will now be described in the following examples which are not intended to limit the scope of the claims hereof.
Additive Concentrate Stability
A base additive concentrate A was prepared which included (on an active ingredient basis, based on the total mass of the base additive concentrate) the following components/diluent oil: a Group I diluent oil (41.9 mass %); polyisobutylenyl succinimide dispersant (28.4 mass %); overhased calcium salicylate detergent TBN 350 mg KOH/g (9.7 mass %) ZDDP (8.3 mass %); molybdenum dithiocarbamate (0.4 mass %); aminic anti-oxidant (8.6 mass %); and glycerol mono-oleate (“GMO”) (2.7 mass %).
The base additive concentrate was used to form a number of different final additive concentrates, as detailed in Table 1, by top-treating identical portions of the base additive concentrate with different polyisobutylenyl succinic anhydrides (PIBSAs) and/or borated dispersant in varying amounts. The final additive concentrates, as detailed in Table 1, differed only in the amount of and/or type of PIBSA, and berated dispersant, contained therein; the type of and amount of other components/diluent oil contributed by the base additive concentrate to each of the final additive concentrates being identical, and as stated in the preceding paragraph. The amount of PIBSA and berated dispersant in each of the final additive concentrates, as detailed in Table 1, is reported on a mass active ingredient basis, based on the total mass of the additive concentrate. For convenience, the amount of calcium salicylate detergent and glycerol mono-oleate (GMO) originating from the base additive concentrate A is also restated in Table 1.
Three different types of polyisobutylenyl succinic anhydrides (PIBSA 1, PIBSA 2 and PIBSA 3) were used to form the final additive concentrates, as detailed in Tables 1 and 2, these are:
The storage stability of each of the final additive concentrates was evaluated as detailed below.
Storage Stability Test Method
100 ml of the sample to be tested is poured into a centrifuge tube and the tube is supported near-vertically in an oven at 60° C. The condition of all samples was observed and noted initially and at weekly/two weekly intervals for 12 weeks. The centrifuge tube was observed under both natural light and a high intensity light source for sediment. The outside of the centrifuge tube was cleaned with solvent, if required, to ensure a clear view. The following observations were made:
1. Evidence of Sediment
2. Visual Inspection
Table 1 below records the pass/fail results from the testing according to the above method.
It can be seen that each PIBSA is, below a certain concentration, not effective per se in stabilising the final concentrate comprising calcium salicylate and GMO. These concentrate examples are designated with the suffix “C”. Thus, whilst PIBSA can stabilise such concentrates, the effect is concentration-dependent and requires the presence of a minimum effective amount in the absence of the berated dispersant.
Addition of the borated dispersant leads to an improvement in the stability of the final concentrates at PIBSA concentration levels that are themselves insufficient to stabilised the concentrate. The improvement is most marked for those concentrates comprising PIBSA 2 having the highest succination ratio of 1.62, where excellent passing stability is achieved even at the relatively low PIBSA level of 2.7 mass (concentrate examples 6 and 7) and low borated dispersant level of 2.3 mass %. At equivalent treat rate, PIBSA 3 (lower succination ratio) requires the higher borated dispersant level of 4.4 mass % to achieve similar stability (concentrate example 11).
Thus, the combined use of borated dispersant and PIBSA in relatively low amounts stabilised the additive concentrate, and enabled the salicylate detergent and organic friction modifier to be packaged together in a single concentrate.
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| 16161582 | Mar 2016 | EP | regional |
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