WO2016156328A1

WO2016156328A1 - Use of a lubricating composition comprising a hindered amine light stabilizer for improved piston cleanliness in an internal combustion engine

Info

Publication number: WO2016156328A1
Application number: PCT/EP2016/056818
Authority: WO
Inventors: Mark Clift Southby; Sergio Leon DE ROOY; Abraham Robert De Kraker
Original assignee: Shell Internationale Research Maatschappij B.V.; Shell Oil Company
Priority date: 2015-03-31
Filing date: 2016-03-29
Publication date: 2016-10-06

Abstract

Use of a lubricating composition comprising (i) base oil and (ii) hindered amine light stabilizer for providing improved piston cleanliness. Preferably, the hindered amine light stabiliser is a 2, 2, 6, 6-tetraalkyl piperidine derivative which contains at least one moiety of formula (I) : wherein R¹, R², R³, and R⁴ are independently selected from C₁-C₈ alkyl or R¹ and R² or R³ and R⁴ together are pentamethylene, and wherein R⁵ is independently selected from hydrogen and C₁-C₈ alkyl.

Description

BRICATING COMPOSITION COMPRISING A HINDERED AMINE LIGHT STABILIZER FOR IMPROVED PISTON CLEANLINESS IN AN INTERNAL COMBUSTION ENGINE

Field of the Invention

The present invention relates to a lubricating

composition, in particular to a lubricating composition which is suitable for lubricating internal combustion

engines and which has improved piston cleanliness

properties .

Background of the Invention

Lubricants may be used in machinery to prevent

friction between moving parts, such as pistons and

cylinders of an engine. In some cases, deposits may form in the lubricants that may hinder the movement of the

parts and, therefore, impact the performance of the

engine. Lubricants may be configured to reduce the

likelihood of deposits and/or affect the performance of the engine.

Lubricants may include a mix of oils and other

additives. The composition of the lubricant may be

selected to define properties which can be used to

enhance performance of the machinery. For example,

various engines may specify the use of a certain

viscosity of lubricant under certain conditions, such as outdoor temperature. In another example, the composition of the lubricant (and/or its additives) may be selected to control the engine' s tendency to oxidize and form

deposits .

It would be desirable to provide a lubricating

composition having improved piston cleanliness

properties .

Hindered amines are chemical compounds containing an amine functional group surrounded by a crowded steric environment. They have uses such as gas scrubbing, as stabilizers against light-induced polymer degradation, and as reagents for organic synthesis. Hindered amine light stabilizers are typically derivatives of 2,2,6,6- tetramethyl piperidine and are extremely efficient stabilizers against light-induced degradation of most polymers .

It has now surprisingly been found by the present inventors that hindered amine light stabilizers can be used to provide improved piston cleanliness properties of a lubricating oil composition for the crankcase of an internal combustion engine.

Summary of the Invention

According to the present invention, there is provided use of a lubricating composition comprising (i) base oil and (ii) hindered amine light stabilizer for providing improved piston cleanliness in an internal combustion engine.

According to another aspect of the present invention there is provided a method for improving the piston cleanliness properties of a lubricating oil composition used to lubricate the crankcase of an internal combustion engine comprising adding to the lubricating oil

composition an additive amount of one or more hindered amine light stabilizers .

Detailed Description of the Invention

As used herein, the term "improved piston

cleanliness" means reducing the amount of piston deposits which are found on the pistons of an internal combustion engine during operation of the engine, in particular as measured according to the hot tube deposits test method disclosed in WO2014036110.

In a preferred embodiment, the % improvement in piston cleanliness provided by the lubricating oil compositions herein is at least a 10% improvement in piston cleanliness, more preferably at least a 15% improvement in piston cleanliness, even more preferably at least a 19% improvement in piston cleanliness, compared to the piston cleanliness of an equivalent lubricating oil composition which does not contain a hindered amine light stabiliser.

In a preferred embodiment of the present invention, the piston cleanliness properties of the lubricating oil composition are measured according to the hot tube deposits test method disclosed in WO2014036110, which reference is incorporated herein by reference in its entirety .

As a first essential component, the lubricating oil composition herein comprises one or more hindered amine light stabilisers, preferably in an amount of from 0.01 wt% to 10 wt%, more preferably in an amount of from 0.25 wt% to 7 wt%, and even more preferably in an amount of from 0.1 wt% to 4 wt%, and especially in an amount of from 0.1 wt% to 2 wt%, by weight of the total lubricating oil composition.

Suitably for use herein the hindered amine light stabiliser is a 2, 2, 6, 6-tetraalkyl piperidine derivative which contains at least one moiety of formula (I) :

(I) wherein R¹, R², R³ and R⁴ are independently selected from Ci-Cs alkyl or R¹ and R² or R³ and R⁴ together are pentamethylene, and wherein R⁵ is independently selected from hydrogen and Ci-C₈ alkyl.

Hindered amine light stabilisers are disclosed for example in US patent nos. 5004770, 5204473, 5096950, 5300544, 5112890, 5124378, 5145893, 5216156, 5844026, 5980783, 6046304, 6117995, 6271377, 6297299, 6392041, 6376584 and 6472456 and US application Ser. Nos.

09/714717 and 10/485377, and US patent application US2007/0151143. The relevant disclosures of these patents and applications are incorporated herein by reference .

US Patent Nos. 6271377, 6392041 and 6376584 cited above disclose hindered hydroxylamine stabilizers.

Suitable hindered amine light stabilizers include, for example, l-cyclohexyloxy-2, 2, 6, 6-tetramethyl-4- octadecylaminopiperidine ; bis (2, 2,6,6- tetramethylpiperidin-4-yl) sebacate; bis (1-acetoxy- 2,2, 6, 6-tetramethylpiperidin-4-yl ) sebacate ;

bis (1, 2, 2, 6, 6-pentamethyl-4-yl) sebacate;

methyl (1, 2, 2, 6, 6-pentamethyl-4-piperidinyl) sebacate, bis (l-cyclohexyloxy-2, 2, 6, 6-tetramethylpiperidin-4-yl) sebacate; bis (l-octyloxy-2, 2, 6, 6-tetramethylpiperidin-4- yl) sebacate; bis (l-acyl-2, 2, 6, 6-tetramethylpiperidin-4- yl) sebacate; bis (1, 2, 2, 6, 6-pentamethyl-4-piperidyl) n- butyl-3, 5-di-tert-butyl-4-hydroxybenzylmalonate; 2, 4- bis [ (l-cyclohexyloxy-2, 2, 6, 6-tetramethylpiperidin-4 -yl ) butylamino] -6- (2-hydroxy-ethylamino-s-triazine; bis (1- cyclohexyloxy-2 , 2, 6, 6-tetramethylpiperidin-4-yl) adipate 2, 4-bis [ (l-cyclohexyloxy-2, 2, 6, 6-piperidin-4-yl) butylamino] -6-chloro-s-triazine; 1- (2-hydroxy-2- methylpropoxy) -4-hydroxy-2, 2, 6, 6-tetramethylpiperidine ; 1- (2-hydroxy-2-methylpropoxy) -4-oxo-2, 2,6,6- tetramethylpiperidine; 1- (2-hydroxy-2-methylpropoxy) -4- octadecanoyloxy-2 , 2, 6, 6-tetramethylpiperidine; bis (1- (2- hydroxy-2-methylpropoxy) -2, 2, 6, 6-tetramethylpiperidin-4- yl) sebacate; bis (1- (2-hydroxy-2-methylpropoxy) -2, 2, 6, 6- tetramethylpiperidin-4-yl) adipate; 2, 4-bis {N- [1- (2- hydroxy-2-methylpropoxy) -2, 2, 6, 6-tetramethylpiperidin-4- yl] -N-butyl-amino } -6- (2-hydroxyethylamino) -s-triazine; 4 benzoyl-2, 2, 6, 6-tetramethylpiperidine; di- (1,2,2,6, 6- pentamethylpiperidin-4-yl ) p-methoxybenzylidenemalonate ; 4 -stearyloxy-2 , 2, 6, 6-tetramethylpiperidine; bis (1- octyloxy-2, 2,6, 6-tetramethylpiperidyl ) succinate ;

1,2,2,6, 6-pentamethyl-4 -aminopiperidine ; 2-undecyl- 7,7,9, 9-tetramethyl-l-oxa-3 , 8-diaza-4-oxo- spiro [4,5] decane; tris (2, 2, 6, 6-tetramethyl-4-piperidyl) nitrilotriacetate; tris (2-hydroxy-3 (-amino- (2, 2, 6, 6- tetramethylpiperidin-4-yl) propyl) nitrilotriacetate ; tetrakis (2, 2, 6, 6-tetramethyl-4-piperidyl) -1, 2, 3, 4-butane tetracarboxylate; tetrakis (1, 2, 2, 6, 6-pentamethyl-4- piperidyl) -1, 2, 3, 4 -butane-tetracarboxylate ; 1, 1' - (1, 2- ethanediyl) -bis (3, 3, 5, 5-tetramethylpiperazinone) ; 3-n- octyl-7, 7, 9, 9-tetramethyl-l , 3, 8-triaza-spiro [4,5] decan- 2, 4-dione; 8-acetyl-3-dodecyl-7 , 7, 9, 9-tetramethyl-l, 3, 8- triazospiro [4,5] decane-2, 4-dione; 3-dodecyl-l- (2, 2, 6, 6- tetramethyl-4-piperidyl) pyrrolidin-2, 5-dione; 3-dodecyl- 1- (1, 2, 2, 6, 6-pentamethy1-4-piperidyl) pyrrolidine-2 , 5- dione ; N.N' -bis-formyl-N, N'-bis(2,2,6, 6-tetramethyl-4- piperidyl ) hexamethylenediamine ; and the following compounds :

the reaction product of 2, 4-bis [ (1-cyclo-hexyloxy- 2,2,6, 6-piperidin-4-yl) butylamino] -6-chloro-s-triazine with Ν,Ν' -bis ( 3-aminopropyl ) ethylenediamine ;

the condensate of 1- (2-hydroxyethyl) -2, 2, 6, 6-tetramethyl 4 -hydroxypiperidine and succinic acid;

linear or cyclic condensates of N, N' -bis (2, 2, 6, 6- tetramethyl-4-piperidyl) -hexamethylenediamine and 4-tert- octylamino-2 , 6-dichloro-l , 3, 5-triazine;

linear or cyclic condensates of N, N' -bis (2, 2, 6, 6- tetramethyl-4-piperidyl) -hexamethylenediamine and 4- cyclohexylamino-2 , 6-dichloro-l, 3, 5-triazine;

linear or cyclic condensates of N, N' -bis (2, 2, 6, 6- tetramethyl-4-piperidyl) -hexamethylenediamine and 4- morpholino-2 , 6-dichloro-l, 3, 5-triazine;

linear or cyclic condensates of N, N' -bis ( 1 , 2 , 2 , 6 , 6- pentamethyl-4 -piperidyl ) -hexamethylenediamine and 4- morpholino-2 , 6-dichloro-l, 3, 5-triazine;

the condensate of 2-chloro-4 , 6-bis (4-n-butylamino-

2, 2, 6, 6-tetramethylpiperidyl) -1, 3, 5-triazine and 1,2- bis (3-aminopropylamino) ethane;

the condensate of 2-chloro-4 , 6-bis (4-n-butylamino-

1, 2, 2, 6, 6-pentamethylpiperidyl) -1, 3, 5-triazine and 1,2- bis (3-aminopropylamino) ethane;

a reaction product of 7, 7, 9, 9-tetramethyl-2-cycloundecyl- l-oxa-3, 8-diaza-4-oxospiro [4,5] decane and

epichlorohydrin ;

poly [methyl, (3-oxy- (2,2,6, 6-tetramethylpiperidin-4- yl) propyl) ] siloxane, CAS#182635-99-0 ;

reaction product of maleic acid anhydride-Ci₈-C₂2^_alpha- olefin-copolymer with 2, 2, 6, 6-tetramethyl-4- aminopiperidine ;

the oligomeric compound which is the condensation product of 4,4' -hexamethylene-bis (amino-2, 2, 6, 6- tetramethylpiperidine) and 2, 4-dichloro-6- [ (2, 2, 6, 6- tetramethylpiperidin-4-yl) butylamino] -s-triazine end- capped with 2-chloro-4 , 6-bis (dibutylamino) -s-triazine; the oligomeric compound which is the condensation product of 4,4' -hexamethylene-bis (amino-1, 2, 2, 6, 6- pentamethylpiperidine ) and 2, 4-dichloro-6- [ (1, 2, 2, 6, 6- pentamethylpiperidin-4-yl) utylamino] -s-triazine end- capped with 2-chloro-4 , 6-bis (dibutylamino) -s-triazine; the oligomeric compound which is the condensation product of 4,4' -hexamethylene-bis (amino-l-propoxy-2 , 2, 6, 6- tetramethylpiperidine) and 2, 4-dichloro-6- [ (1-propoxy- 2,2, 6, 6-tetramethylpiperin-4 -yl ) butylamino] -s-triazine end-capped with 2-chloro-4 , 6-bis (dibutylamino) -s- triazine ;

the oligomeric compound which is the condensation product of 4,4' -hexamethylene-bis (amino-l-acyloxy-2 , 2, 6, 6- tetramethylpiperidine) and 2, 4-dichloro-6- [ (1-acyloxy- 2,2, 6, 6-tetramethylpiperin-4 -yl ) butylamino] -s-triazine end-capped with 2-chloro-4 , 6-bis (dibutylamino) -s- triazine; and

product obtained by reacting 1, 2-bis (3-amino- propylamino) ethane with cyanuric chloride, with (2,2,6,6- tetramethylpiperidin-4-yl) butylamine .

Also included are the sterically hindered N-H, N- methyl, N-methoxy, N-propoxy, N-octyloxy, N- cyclohexyloxy, N-acyloxy and N- (2-hydroxy-2- methylpropoxy) analogues of any of the above mentioned compounds. For example, replacing an N-H hindered amine with an N-methyl hindered amine would be employing the N- methyl analogue in place of the N-H.

Preferred hindered amine light stabilizers for use herein are selected from bis (l-octyloxy-2, 2, 6, 6- tetramethyl-4-piperidinyl) sebacate, bis (2, 2,6,6- tetramethyl-4-piperidinyl) sebacate, bis (1, 2,2,6, 6- pentamethyl-4 -piperidinyl ) sebacate, methyl (1,2,2,6, 6- pentamethyl-4 -piperidinyl ) sebacate, and mixtures thereof.

Examples of commercially available hindered amine light stabilisers suitable for use herein include those compounds available from Mayzo under the tradenames BLS 1770 and BLS 292.

There are no particular limitations regarding the base oil used in lubricating composition according to the present invention, and various conventional mineral oils, synthetic oils as well as naturally derived esters such as vegetable oils may be conveniently used.

The base oil used in the lubricating compositions herein may conveniently comprise mixtures of one or more mineral oils and/or one or more synthetic oils; thus, according to the present invention, the term "base oil" may refer to a mixture containing more than one base oil. Mineral oils include liquid petroleum oils and solvent- treated or acid-treated mineral lubricating oil of the paraffinic, naphthenic, or mixed paraffinic/naphthenic type which may be further refined by hydrofinishing processes and/or dewaxing.

Suitable base oils for use in the lubricating oil composition herein are Group I-III mineral base oils, Group IV poly-alpha olefins (PAOs), Group II-III Fischer- Tropsch derived base oils (preferably Group III), Group V ester base oils, and mixtures thereof.

By "Group I", "Group II" "Group III" and "Group IV" and "Group V" base oils as used herein are meant

lubricating oil base oils according to the definitions of American Petroleum Institute (API) for categories I, II, III, IV and V. These API categories are defined in API Publication 1509, 15th Edition, Appendix E, April 2002.

Fischer-Tropsch derived base oils are known in the art . By the term "Fischer-Tropsch derived" is meant that a base oil is, or is derived from, a synthesis product of a Fischer-Tropsch process. A Fischer-Tropsch derived base oil may also be referred to as a GTL (Gas-To- Liquids) base oil. Suitable Fischer-Tropsch derived base oils that may be conveniently used as the base oil in the lubricating composition herein are those as for example disclosed in EP0776959, EP0668342, W09721788, WO0015736, WO0014188, WO0014187, WO0014183, WO0014179, WO0008115, W09941332, EP1029029, WO0118156 and WO0157166.

Typically, the aromatics content of a Fischer- Tropsch derived base oil, suitably determined by ASTM D 4629, will typically be below 1 wt%, preferably below 0.5 wt% and more preferably below 0.1 wt%. Suitably, the base oil has a total paraffin content of at least 80 wt%, preferably at least 85, more preferably at least 90, yet more preferably at least 95 and most preferably at least 99 wt%. It suitably has a saturates content (as measured by IP-368) of greater than 98 wt%. Preferably the saturates content of the base oil is greater than 99 wt%, more preferably greater than 99.5 wt%. It further preferably has a maximum n-paraffin content of 0.5 wt%. The base oil preferably also has a content of naphthenic compounds of from 0 to less than 20 wt%, more preferably of from 0.5 to 10 wt%.

Typically, the Fischer-Tropsch derived base oil or base oil blend has a kinematic viscosity at 100°C (as measured by ASTM D 7042) in the range of from 1 to 30 mm²/s (cSt), preferably from 1 to 25 mm²/s (cSt), and more preferably from 2 mm²/s to 12 mm²/s. Preferably, the Fischer-Tropsch derived base oil has a kinematic viscosity at 100°C (as measured by ASTM D 7042) of at least 2.5 mm²/s, more preferably at least 3.0 mm²/s. In one embodiment of the present invention, the Fischer- Tropsch derived base oil has a kinematic viscosity at more preferably at most 4.2 mm /s (e.g. "GTL 4") . In another embodiment of the present invention, the Fischer- Tropsch derived base oil has a kinematic viscosity at 100°C of at most 8.5 mm²/s, preferably at most 8 mm²/s (e.g. "GTL 8") .

Further, the Fischer-Tropsch derived base oil typically has a kinematic viscosity at 40°C (as measured by ASTM D 7042) of from 10 to 100 mm²/s (cSt), preferably from 15 to 50 mm²/s.

Also, the Fischer-Tropsch derived base oil

preferably has a pour point (as measured according to ASTM D 5950) of below -30°C, more preferably below -40°C, and most preferably below -45°C.

The flash point (as measured by ASTM D92) of the Fischer-Tropsch derived base oil is preferably greater than 120°C, more preferably even greater than 140°C.

The Fischer-Tropsch derived base oil preferably has a viscosity index (according to ASTM D 2270) in the range of from 100 to 200. Preferably, the Fischer-Tropsch derived base oil has a viscosity index of at least 125, preferably 130. Also it is preferred that the viscosity index is below 180, preferably below 150.

In the event the Fischer-Tropsch derived base oil contains a blend of two or more Fischer-Tropsch derived base oils, the above values apply to the blend of the two or more Fischer-Tropsch derived base oils.

The lubricating oil composition herein preferably comprises 80 wt% or greater of Fischer-Tropsch derived base oil.

Synthetic oils include hydrocarbon oils such as olefin oligomers (including polyalphaolefin base oils; PAOs), dibasic acid esters, polyol esters, polyalkylene glycols (PAGs), alkyl naphthalenes and dewaxed waxy isomerates. Synthetic hydrocarbon base oils sold by the Shell Group under the designation "Shell XHVI" (trade mark) may be conveniently used.

Poly-alpha olefin base oils (PAOs) and their manufacture are well known in the art. Preferred poly- alpha olefin base oils that may be used in the

lubricating compositions of the present invention may be derived from linear C₂ to C₃₂, preferably C₆ to Ci₆, alpha olefins. Particularly preferred feedstocks for said poly-alpha olefins are 1-octene, 1-decene, 1-dodecene and 1-tetradecene .

There is a strong preference for using a Fischer- Tropsch derived base oil over a PAO base oil, in view of the high cost of manufacture of the PAOs. Thus,

preferably, the base oil contains more than 50 wt%, preferably more than 60 wt%, more preferably more than 70 wt%, even more preferably more than 80 wt . % . most preferably more than 90 wt% Fischer-Tropsch derived base oil. In an especially preferred embodiment not more than 5 wt%, preferably not more than 2 wt%, of the base oil is not a Fischer-Tropsch derived base oil. It is even more preferred that 100 wt% of the base oil is based on one or more Fischer-Tropsch derived base oils.

The total amount of base oil incorporated in the lubricating composition herein is preferably in the range of from 60 to 99 wt%, more preferably in the range of from 65 to 90 wt% and most preferably in the range of from 70 to 85 wt%, with respect to the total weight of the lubricating composition.

Typically the base oil (or base oil blend) as used in the lubricating composition herein has a kinematic viscosity at 100°C (according to ASTM D445) of above 2.5 cSt and below 5.6 cSt . According to a preferred embodiment of the present invention the base oil has a kinematic viscosity at 100°C (according to ASTM D445) of between 3.5 and 4.5 cSt . In the event the base oil contains a blend of two or more base oils, it is

preferred that the blend has a kinematic viscosity at 100°C of between 3.5 and 4.5 cSt .

Typically the lubricating compositions herein would be utilised in, but not necessarily limited to, SAE J300 viscosity grades OW-20, OW-30, OW-40, 5W-20, 5W-30 and 5W-40 as these are the grades which target fuel economy. As new SAE J300 viscosity grades are published, with lower viscosities than the current OW-20, the present invention would also be very much applicable to these new viscosity lower grades. It is conceivable that the present invention could also be used with higher

viscosity grades.

The lubricating composition herein preferably has a Noack volatility (according to ASTM D 5800) of below 15 wt%. Typically, the Noack volatility (according to ASTM D 5800) of the composition is between 1 and 15 wt%, preferably below 14.6 wt% and more preferably below 14.0 wt% .

Preferably, the lubricating oil composition has a kinematic viscosity in the range of from 2 to 80 mm²/s at 100 °C, more preferably of from 3 to 70 mm²/s, most preferably of from 4 to 50 mm²/s.

The total amount of phosphorus in the lubricating oil composition herein is preferably less than or equal to 0.08 wt%, by weight of the lubricating composition.

The lubricating oil composition herein preferably has a sulphated ash content of not greater than 2.0 wt%, more preferably not greater than 1.0 wt% and most preferably not greater than 0.8 wt%, based on the total weight of the lubricating oil composition.

The lubricating oil composition herein preferably has a sulphur content of not greater than 1.2 wt%, more preferably not greater than 0.8 wt% and most preferably not greater than 0.2 wt%, based on the total weight of the lubricating oil composition.

The lubricating composition herein further comprises one or more additives such as anti-oxidants, anti-wear additives, dispersants, detergents, overbased detergents, extreme pressure additives, friction modifiers, viscosity index improvers, pour point depressants, metal

passivators, corrosion inhibitors, demulsifiers , anti-foam agents, seal compatibility agents and additive diluent base oils, etc.

As the person skilled in the art is familiar with the above and other additives, these are not further discussed here in detail. Specific examples of such additives are described in for example Kirk-Othmer

Encyclopedia of Chemical Technology, third edition, volume 14, pages 477-526.

Antioxidants that may be conveniently used include those selected from the group of aminic antioxidants and/or phenolic antioxidants. In a preferred embodiment, said antioxidants are present in an amount in the range of from 0.1 to 5.0 wt%, more preferably in an amount in the range of from 0.3 to 3.0 wt%, and most preferably in an amount in the range of from 0.5 to 1.5 wt%, based on the total weight of the lubricating oil composition.

Examples of aminic antioxidants which may be

conveniently used include alkylated diphenylamines, phenyl-a-naphthylamines, phenyl--naphthylamines and alkylated a-naphthylamines .

Preferred aminic antioxidants include dialkyldiphenylamines such as p, p ' -dioctyl-diphenylamine, p, p ' -di-a-methylbenzyl-diphenylamine and N-p-butylphenyl- N-p ' -octylphenylamine, monoalkyldiphenylamines such as mono-t-butyldiphenylamine and mono-octyldiphenylamine, bis (dialkylphenyl) amines such as di-(2,4- diethylphenyl) amine and di (2-ethyl-4-nonylphenyl) amine, alkylphenyl-l-naphthylamines such as octylphenyl-1- naphthylamine and n-t-dodecylphenyl-l-naphthylamine, 1- naphthylamine, arylnaphthylamines such as phenyl-1- naphthylamine, phenyl-2-naphthylamine, N-hexylphenyl-2- naphthylamine and N-octylphenyl-2-naphthylamine,

phenylenediamines such as N, ' -diisopropyl-p- phenylenediamine and N, ' -diphenyl-p-phenylenediamine, and phenothiazines such as phenothiazine and 3,7- dioctylphenothiazine .

Preferred aminic antioxidants include those available under the following trade designations: "Sonoflex OD-3" (ex. Seiko Kagaku Co.), "Irganox L-57" (ex. Ciba

Specialty Chemicals Co.) and phenothiazine (ex. Hodogaya Kagaku Co . ) .

Examples of phenolic antioxidants which may be conveniently used include C₇-C₉ branched alkyl esters of 3, 5-bis (1, 1-dimethyl-ethyl ) -4-hydroxy-benzenepropanoic acid, 2-t-butylphenol, 2-t-butyl-4-methylphenol, 2-t- butyl-5-methylphenol, 2, 4-di-t-butylphenol, 2, 4-dimethyl-

6-t-butylphenol, 2-t-butyl-4-methoxyphenol, 3-t-butyl-4- methoxyphenol, 2, 5-di-t-butylhydroquinone, 2, 6-di-t-butyl- 4-alkylphenols such as 2, 6-di-t-butylphenol, 2,6-di-t- butyl-4-methylphenol and 2, 6-di-t-butyl-4-ethylphenol, 2, 6-di-t-butyl-4-alkoxyphenols such as 2, 6-di-t-butyl-4- methoxyphenol and 2, 6-di-t-butyl-4-ethoxyphenol, 3,5-di-t- butyl-4-hydroxybenzylmercaptooctylacetate, alkyl-3- (3, 5- di-t-butyl-4-hydroxyphenyl) propionates such as n- octadecyl-3- (3, 5-di-t-butyl-4-hydroxyphenyl) propionate, n- butyl-3- (3, 5-di-t-butyl-4-hydroxyphenyl) propionate and 2'- ethylhexyl-3- (3, 5-di-t-butyl-4-hydroxyphenyl) propionate,

2, 6-d-t-butyl-OC-dimethylamino-p-cresol, 2,2' -methylene- bis (4-alkyl-6-t-butylphenol) such as 2, 2 ' -methylenebis (4- methyl-6-t-butylphenol, and 2, 2-methylenebis (4-ethyl-6-t- butylphenol) , bisphenols such as 4 , 4 ' -butylidenebis ( 3- methyl-6-t-butylphenol, 4,4' -methylenebis (2, 6-di-t- butylphenol) , 4 , 4 ' -bis (2 , 6-di-t-butylphenol ) , 2,2-(di-p- hydroxyphenyl) propane, 2, 2-bis (3, 5-di-t-butyl-4- hydroxyphenyl) propane, 4,4' -cyclohexylidenebis (2, 6-t- butylphenol) , hexamethyleneglycol-bis [3- (3, 5-di-t-butyl-4- hydroxyphenyl) propionate] , triethyleneglycolbis [3- (3-t- butyl-4-hydroxy-5-methylphenyl) propionate] , 2,2' -thio- [diethyl-3- (3, 5-di-t-butyl-4-hydroxyphenyl) propionate] ,

3 , 9-bis { 1 , 1 -dimethyl-2- [3- ( 3 -t -buty1-4 -hydroxy-5-methyl- phenyl) propionyloxy ] ethyl } 2, 4, 8, 10- tetraoxaspiro [5,5] undecane, 4,4' -thiobis (3-methyl-6-t- butylphenol) and 2 , 2 ' -thiobis ( 4 , 6-di-t-butylresorcinol ) , polyphenols such as tetrakis [methylene-3- (3, 5-di-t-butyl-

4 -hydroxyphenyl) propionate ] methane, 1,1, 3-tris (2-methyl-4- hydroxy-5-t-butylphenyl) butane, 1,3, 5-trimethyl-2 , 4, 6- tris (3, 5-di-t-butyl-4-hydroxybenzyl ) benzene, bis- [3, 3 ' - bis (4 ' -hydroxy-3 ' -t-butylphenyl) butyric acid] glycol ester, 2- (3 ' , 5 ' -di-t-butyl-4-hydroxyphenyl)methyl-4- (2", 4"-di-t- butyl-3"-hydroxyphenyl)methyl-6-t-butylphenol and 2,6- bis (2 ' -hydroxy-3 ' -t-butyl-5 ' -methylbenzyl ) -4-methylphenol, and p-t-butylphenol - formaldehyde condensates and p-t- butylphenol - acetaldehyde condensates.

Preferred phenolic antioxidants include those available under the following trade designations:

"Irganox L-135" (ex. Ciba Specialty Chemicals Co.),

"Yoshinox SS" (ex. Yoshitomi Seiyaku Co.), "Antage W-400" (ex. Kawaguchi Kagaku Co.), "Antage W-500" (ex. Kawaguchi Kagaku Co.), "Antage W-300" (ex. Kawaguchi Kagaku Co.), "Irganox L109" (ex. Ciba Speciality Chemicals Co.),

"Tominox 917" (ex. Yoshitomi Seiyaku Co.), "Irganox L115"

(ex. Ciba Speciality Chemicals Co.), "Sumilizer GA80" (ex. Sumitomo Kagaku), "Antage RC" (ex. Kawaguchi Kagaku Co.), "Irganox L101" (ex. Ciba Speciality Chemicals Co.),

"Yoshinox 930" (ex. Yoshitomi Seiyaku Co.) .

The lubricating oil composition herein may comprise mixtures of one or more phenolic antioxidants with one or more aminic antioxidants.

Anti-wear additives that may be conveniently used include zinc-containing compounds such as zinc

dithiophosphate compounds selected from zinc dialkyl-, diaryl- and/or alkylaryl- dithiophosphates , molybdenum- containing compounds, boron-containing compounds and ashless anti-wear additives such as substituted or unsubstituted thiophosphoric acids, and salts thereof.

In a preferred embodiment, the lubricating oil composition may comprise a single zinc dithiophosphate or a combination of two or more zinc dithiophosphates as anti-wear additives, the or each zinc dithiophosphate being selected from zinc dialkyl-, diaryl- or alkylaryl- dithiophosphates .

Zinc dithiophosphate is a well known additive in the art and may be conveniently represented by general formula II;

s s wherein R^z to R may be the same or different and are each a primary alkyl group containing from 1 to 20 carbon atoms preferably from 3 to 12 carbon atoms, a secondary alkyl group containing from 3 to 20 carbon atoms, preferably from 3 to 12 carbon atoms, an aryl group or an aryl group substituted with an alkyl group, said alkyl substituent containing from 1 to 20 carbon atoms

preferably 3 to 18 carbon atoms.

Zinc dithiophosphate compounds in which to are all different from each other can be used alone or in admixture with zinc dithiophosphate compounds in which R² to R⁵ are all the same.

Preferably, the or each zinc dithiophosphate used in the present invention is a zinc dialkyl dithiophosphate.

Examples of suitable zinc dithiophosphates which are commercially available include those available ex.

Lubrizol Corporation under the trade designations "Lz

1097" and "Lz 1395", those available ex. Chevron Oronite under the trade designations "OLOA 267" and "OLOA 269R", and that available ex. Afton Chemical under the trade designation "HITEC 7197"; zinc dithiophosphates such as those available ex. Lubrizol Corporation under the trade designations "Lz 677A", "Lz 1095" and "Lz 1371", that available ex. Chevron Oronite under the trade designation "OLOA 262" and that available ex. Afton Chemical under the trade designation "HITEC 7169"; and zinc

dithiophosphates such as those available ex. Lubrizol

Corporation under the trade designations "Lz 1370" and "Lz 1373" and that available ex. Chevron Oronite under the trade designation "OLOA 260".

The lubricating oil composition herein may generally comprise in the range of from 0.4 to 1.2 wt% of zinc dithiophosphate, based on total weight of the lubricating oil composition.

Examples of such molybdenum-containing compounds may conveniently include molybdenum dithiocarbamates , trinuclear molybdenum compounds, for example as described in WO 98/26030, sulphides of molybdenum and molybdenum dithiophosphate .

Boron-containing compounds that may be conveniently used include borate esters, borated fatty amines, borated epoxides, alkali metal (or mixed alkali metal or alkaline earth metal) borates and borated overbased metal salts.

Typical detergents that may be used in the

lubricating composition herein include one or more salicylate and/or phenate and/or sulphonate detergents.

However, as metal organic and inorganic base salts which are used as detergents can contribute to the sulphated ash content of a lubricating oil composition, in a preferred embodiment of the present invention, the amounts of such additives are minimised.

Furthermore, in order to maintain a low sulphur level, salicylate detergents are preferred.

In order to maintain the total sulphated ash content of the lubricating oil composition herein at a level of preferably not greater than 2.0 wt%, more preferably at a level of not greater than 1.0 wt% and most preferably at a level of not greater than 0.8 wt%, based on the total weight of the lubricating oil composition, said

detergents are preferably used in amounts in the range of

0.05 to 20.0 wt%, more preferably from 1.0 to 10.0 wt% and most preferably in the range of from 2.0 to 5.0 wt%, based on the total weight of the lubricating oil

composition .

Furthermore, it is preferred that said detergents, independently, have a TBN (total base number) value in the range of from 10 to 500 mg.KOH/g, more preferably in the range of from 30 to 350 mg.KOH/g and most preferably in the range of from 50 to 300 mg.KOH/g, as measured by ISO 3771.

The lubricating oil compositions herein may

additionally contain an ash-free dispersant which is preferably admixed in an amount in the range of from 5 to 15 wt%, based on the total weight of the lubricating oil composition .

Examples of ash-free dispersants which may be used include the polyalkenyl succinimides and polyalkenyl succininic acid esters disclosed in Japanese Patent Nos . 1367796, 1667140, 1302811 and 1743435. Preferred dispersants include borated succinimides.

Examples of viscosity index improvers which may conveniently be used in the lubricating composition herein include the styrene-butadiene stellate copolymers, styrene-isoprene stellate copolymers and the

polymethacrylate copolymer and ethylene-propylene copolymers (also known as olefin copolymers) of the crystalline and non-crystalline type. Dispersant- viscosity index improvers may be used in the lubricating composition herein. However, preferably the composition herein contains less than 1.0 wt%, preferably less than 0.5 wt%, of a Viscosity Index improver concentrate (i.e. VI improver plus "carrier oil" or "diluent"), based on the total weight of the composition. Most preferably, the composition is free of Viscosity Index improver concentrate. The term "Viscosity Modifier" as used hereafter is meant to be the same as the above-mentioned term "Viscosity Index improver concentrate".

Preferably, the composition contains at least 0.1 wt% of a pour point depressant. As an example, alkylated naphthalene and phenolic polymers, polymethacrylates, maleate/ fumarate copolymer esters may be conveniently used as effective pour point depressants. Preferably not more than 0.3 wt% of the pour point depressant is used.

Furthermore, compounds such as alkenyl succinic acid or ester moieties thereof, benzotriazole-based compounds and thiodiazole-based compounds may be conveniently used in the lubricating composition herein as corrosion inhibitors .

Compounds such as polysiloxanes, dimethyl

polycyclohexane and polyacrylates may be conveniently used in the lubricating composition herein as defoaming agents.

Compounds which may be conveniently used in the lubricating composition herein as seal fix or seal compatibility agents include, for example, commercially available aromatic esters.

The above-mentioned additives are typically present in an amount in the range of from 0.01 to 35.0 wt%, based on the total weight of the lubricating composition, preferably in an amount in the range of from 0.05 to 25.0 wt%, more preferably from 1.0 to 20.0 wt%, based on the total weight of the lubricating composition.

Preferably, the composition contains at least 9.0 wt%, preferably at least 10.0 wt%, more preferably at least 11.0 wt% of an additive package comprising an anti- wear additive, a metal detergent, an ashless dispersant and an anti-oxidant .

The lubricating compositions herein are preferably engines oils for use in the crankcase of an engine. The engine oil may include a heavy duty diesel engine oil, a passenger car motor engine oil, as well as other types of engine oils, such as motor cycle oils and marine engine oils .

The lubricating compositions herein may be so-called "low SAPS" (SAPS = sulphated ash, phosphorus and sulphur), "mid SAPS" or "regular SAPS" formulations.

For Passenger Car Motor Oil (PCMO) engine oils the above ranges mean:

a sulphated ash content (according to ASTM D 874) of up to 0.5 wt%, up to 0.8 wt% and up to 1.5 wt%,

respectively;

a phosphorus content (according to ASTM D 5185) of up to 0.05 wt%, up to 0.08 wt% and typically up to 0.1 wt%, respectively; and

a sulphur content (according to ASTM D 5185) of up to 0.2 wt%, up to 0.3 wt% and typically up to 0.5 wt%, respectively.

For Heavy Duty Diesel Engine Oils the above ranges mean :

a sulphated ash content (according to ASTM D 874) of up to 1 wt%, up to 1 wt% and up to 2 wt%, respectively; a phosphorus content (according to ASTM D 5185) of up to 0.08 wt% (low SAPS) and up to 0.12 wt% (mid SAPS), respectively; and

a sulphur content (according to ASTM D 5185) of up to 0.3 wt% (low SAPS) and up to 0.4 wt% (mid SAPS), respectively.

The lubricating compositions herein may be

conveniently prepared using conventional formulation techniques by admixing base oil with the hindered amine light stabiliser and other additive components/additive package at a temperature of, for example, around 60 °C.

It has surprisingly been found that the lubricating compositions described herein containing the

abovementioned hindered amine light stabiliser provides reduced piston cleanliness, in particular as measured according to hot tube deposits test method as described in WO2014036110. In the hot tube deposits test method as described in WO2014036110 a cleanliness merit of 10.0 represents completely clean engine pistons. The

lubricating compositions described herein comprising a base oil and a hindered amine light stabiliser preferably provide a hot tube cleanliness merit result in the hot tube deposits test method described in WO2014036110 of 8.0 or above .

The present invention is described below with reference to the following Examples, which are not intended to limit the scope of the present invention in any way .

Examples

Lubricating formulations were prepared by top treating a reference lubricant (reference lubricant A which was a passenger car motor oil (PCMO) meeting GF-5 specification) with 3wt% of a hindered amine light stabilizer compound or a conventional antioxidant

compound. Comparative Example 1 consisted of reference lubricant A top treated with 3wt% of a conventional aminic antioxidant. Comparative Example 2 consisted of reference lubricant A top treated with 3wt% of a conventional phenolic antioxidant. Example 1 consisted of the

reference lubricant A top treated with 3wt% of decanedioic acid, 1, 10-bis (2, 2, 6, 6-tetramethyl-4-piperidinyl) ester (commercially available from Mayzo under the tradename BLS

1770) . Example 2 consisted of reference lubricant A top treated with 3 wt% of decanedioic acid, 1, 10-bis

(1, 2, 2, 6, 6-pentamethyl-4-piperidinyl) ester + decanedioic acid, 1-methyl 10-1, 2, 2, 6, 6-pentamethyl-4- piperidinyl ) ester (commercially available from Mayzo under the tradename BLS 292) . Examples 1 and 2 were subjected to the hot tube deposits test method described in

WO2014036110. The results of these experiments are set out in Table 1 below. A hot tube cleanliness merit result of 10 means completely clean. A hot tube cleanliness merit result over 8 demonstrates excellent piston cleanliness.

Table 1

Discussion

As shown in Table 1, both Examples 1 and 2 showed a hot tube cleanliness merit result of 8.1. This compared to hot tube cleanliness merit results of 7.5 and 6.9 for Comparative Example 1 and Comparative Example 2,

respectively. These results demonstrate that lubricating compositions top treated with 3 wt% of a hindered amine light stabiliser compound demonstrate improved piston cleanliness compared with comparative compositions top treated with conventional aminic/phenolic antioxidants.

Claims

C L A I M S

1. Use of a lubricating composition comprising (i) base oil and (ii) hindered amine light stabilizer for

providing improved piston cleanliness in an internal combustion engine.

2. Use according to Claim 1 wherein the hindered amine light stabiliser is a 2, 2, 6, 6-tetraalkyl piperidine derivative which contains at least one moiety of formula I :

(I)

wherein R¹, R², R³, and R⁴ are independently selected from Ci-C₈ alkyl or R¹ and R² or R³ and R⁴ together are

pentamethylene, and wherein R⁵ is independently selected from hydrogen and Ci-C₈ alkyl.

3. Use according to Claim 1 or 2 wherein the hindered amine light stabiliser is selected from bis (1-octyloxy- 2, 2, 6, 6-tetramethyl-4-piperidyl) sebacate, bis (2, 2,6,6- tetramethyl-4-piperidyl) sebacate, bis (1,2,2,6, 6- pentamethyl-4-piperidyl) sebacate, methyl (1,2,2,6,6- pentamethyl-4 -piperidinyl ) sebacate, and mixtures thereof.

4. Use according to any of Claims 1 to 3 wherein the hindered amine light stabiliser is present in the lubricating composition at a level of from 0.1 wt% to 6 wt%, by weight of the lubricating composition.

5. Use according to any of Claims 1 to 4 wherein the hindered amine light stabiliser is present in the lubricating composition at a level of from 0.5 to 5 wt%, by weight of the lubricating composition.

6. Use according to any of Claims 1 to 5 wherein the lubricating composition additionally comprises a performance additive.

7. Use according to any of Claims 1 to 6 wherein the lubricating composition comprises from 60 wt% to 99 wt% of base oil.

8. Use according to any of Claims 1 to 7 wherein the base oil comprises a Fischer-Tropsch derived base oil.

9. Method for improving the piston cleanliness properties of a lubricating oil composition used to lubricate the crankcase of an internal combustion engine comprising adding to the lubricating oil composition an additive amount of one or more hindered amine light stabilizers .