AU689911B2 - Shear stable lubricating compositions - Google Patents

Description

OPI DATE 05/01/96 AOJP DATE 15/02/96 APPLN, ID 27913/95 PCT NUMBER PCT/EP95/02270 I llIIII ll I l I l I 1 1111 II I AU9527913

INT,

(51) International Patent Classification 6 (11) International Publication Number: WO 95/34617 161/00 (C10M 161/00, 129:95, Al 133:52, 143:00), C10N 20:02, 30:04, (43) International Publication Date: 21 December 1995 (21.12.95) 40:25 (21) International Apolication Number: PCT/EP95/02270 (81) Designated States: AU, CA, JP, SG, European patent (AT, BE, CH, DE, DK, ES, FR, GB, GR, IE, IT, LU, MC, NL, PT, (22) International Filing Date: 12 June 1995 (12.06,95) SE).

Priority Data: Published 9412063.1 16 June 1994 (16.06,94) GB With international search report.

9412102.7 16 June 1994 (16,06,94) GB Before the expiration of the time limit for amending the claims and to be republished in the event of the receipt of amendments, (71) Applicants: EXXON CHEMICAL LIMITED [GB/GB]; Exxon Chemical Technology Centre, P.O. Box 1, Abingdon, Oxfordshire OX13 6BB EXXON CHEMICAL PATENTS INC. [US/US]; 1900 East Linden Avenue, Linden, NJ 07036 (US).

(72) Inventors: ADAMS, David, Robert; Cornerstones, High Street, Hinton Waldrist, Faringdon, Oxfordshire SN7 8RN (GB), BRICE, Paul; 22 Galley Field, Abingdon, Oxfordshire OX14 3RT (GB), (74) Agents: NORTHOVER, Robert, Frank et al.; Exxon Chemical Limited, Exxon Chemical Technology Centre, P.O. Box 1, Abingdon, Oxfordslire OX13 6BB (GB).

(54) Title: SHEAR STABLE LUBRICATING COMPOSITIONS (57) Abstract This invention relates to shear stable lubricating compositions, particularly multigrade oils for crankcase lubrication of gasoline and diesel engines. Multigrade crankcase oils are formulated with an ashless dispersant comprising an oil soluble polymeric hydrocarbon backbone having functional groups in which the hydrocarbon backbone is derived from an ethylene alpha-olefin (EAO) copolymer or alphaolefin homo- or copolymer having an Mn of from 500 to 7000. They provide better fuel economy and better starting at cold temperatures.

More economical multigrade crankcase oils may also be blended with less shear stable VMs for improved economy, with a possibility of employing a wider range of polymers. Oils may be blended having extremely good oil shear stability for the most demanding applications where high performance is required such as in turbocharged engines and racing engines, with reduced mechanical breakdown of the oil.

WO 95/34617 PCT/EP95/02270 Shear stable lubricating compositions This invention relates to shear stable lubricating compositions, particularly multigrade oils for crankcase lubrication of gasoline and diesel engines.

Lubricating oils used in gasoline and diesel crankcases comprise a natural and/or synthetic basestock containing one or more additives to impart desired characteristics to the lubricant, Such additives typically include ashless dispersant, metal detergent, antioxidant and antiwear components, which may be combined in a package, sometimes referred to as a detergent inhibitor (or DI) package. The additives in such a package may include functionalised polymers but these have relatively short chains, typically having a number average molecular weight M of not not more than 7000.

Multigrade oils usually also contain one or more viscosity modifiers (VM) which are longer chain polymers, which may be functionalised to provide other properties when they are known as multifunctional VMs (or MFVMs), but primarily act to improve the viscosity characteristics of the oil over the operating range. Thus the VM acts to increase viscosity at high temperature to provide more protection to the engine at high speeds, without unduly increasing viscosity at low temperatures which would otherwise make starting a cold engine difficult. High temperature performance is usually measured in terms of the kinematic viscosity (kV) at 100 C (ASTM D445), while low temperature performance is measured in terms of cold cranking simulator (CCS) viscosity (ASTM D5293, which is a revision of ASTM D2602).

Viscosity grades are defined by the SAE Classification system according to these two temperature measurements. SAE J300 defines the following grades: WO 95/34617 PCT/EP95/02270 2 SAE VISCOSITY GRADES SAE viscosity Maximum CCS kV 100oC mm 2 /s kV 100 0 C mm 2 /s grade Viscosity minimum maximum 3 Pa.s (OC) 3500 3.8 3500 4.1 3500 5.6 4500 5.6 6000 9.3 5.6 <9.3 -9.3 <12.5 12.5 <16.3 16.3 <21.9 Multigrade oils meet the requirements of both low temperature and high temperature perfomance, and are thus identified by reference to both relevant grades. For example, a 5W30 multigrade oil has viscosity characteristics that satisfy both the 5W and the 30 viscosity grade requirements i.e. a maximum CCS viscosity of 3500.10- 3 Pa.s at -25 0 C, a minimum kV100°C of 9.3 mm 2 /s and a maximum kV100 0 C of <12.5 mm 2 /s.

Viscosity modifiers comprise polymers having an Mn of at least 20,000. For ease of handling viscosity modifiers are usually employed as oil solutions of such polymers. When used in engines, oils are subjected to high mechanical shear, for example in bearings, pumps and gears, or to chemical attack such as oxidation, and the longer polymer chains of viscosity modifiers are broken which reduces their contribution to viscosity performance.

Shear stability is a measure of the ability of an oil to resist permanent viscosity loss under high shear the more shear stable an oil, the smaller the viscosity loss when subjected to shear. Polymeric viscosity modifiers which make a significant contribution to kV100C are not completely shear stable.

WO 95/34617 PCTIEP95/02270 3 Shear stability of viscosity modifiers or oils containing them may be measured by a number of methods including the Kurt-Orbahn Diesel Fuel Injector test (CEC-L-14-A-88). Oil shear stability is quoted as the loss of kV100C of the oil in the test. VM shear stability is quoted as the shear stability index or SSI of the VM. SSI is the loss of kV100°C in the test by a 14 mm 2 /s solution of the VM in a 5mm 2 /s diluent oil, the loss being expressed as a of the kV100°C contribution of the unsheared VM polymer. The kV100°C contribution of the unsheared VM polymer can be determined by comparing the kV100°C of diluent oil with and without the polymer present. Thus: SSI= (i tf)/(Ti 1o). 100, where ri is the viscosity of the solution of VM in diluent oil, rIo is the viscosity of the diluent oil without VM, and rf is the viscosity of the sheared VM solution.

Specifications for lubricants may be set in terms of a maximum loss of viscosity and/or minimum limit on after shear viscosity. The most severe requirements for oil shear stability at present are for oils that meet the VW500.00 specification and proposed ACEA specification, which require the kV100°C of the oil to be in grade (according to SAE J300) at the end of the shear test and to suffer a kV100 0 C viscosity loss not exceeding 15% in the Kurt-Orbahn Diesel Fuel Injector test. Thus for a multigrade oil meeting the grade requirement of SAE J300 a 15W/40 or 10W/40 oil) the oil must have a minimum kV100°C of 12.5 mm 2 /s at the end of the test and a maximum kV100 0 C viscosity loss of Economic VMs such as olein copolymers have poor shear stability (high SSI). Use of VMs with low SSI tends to be expensive. Conventional shorter chain polymers which are used in functionalised form as dispersants are much more shear stable but marke only a small contribution to kV100°C.

Thus the contribution to kVi 00°C maae by the polyisobutenyl succinimide dispersants described for example in US-A-4234435 is limited. In addition the amount of conventional dispersants is largely dictated by the requirements of sludge and varnish control which is the primary function of the ashless dispersant.

Thus multigrade oils have poor shear stability unless they use expensive VMs with low SSI. Poor shear stability requires the oils to be blended to a higher initial kV100 0 C which results in poorer fuel economy, and proposals for the ILSAC GF-2 specification for passenger car engine oils require demonstration of fuel economy performance in an ASTM Sequence VIA engine test. In addition very high levels of shear stability for high performance applications cannot be achieved.

A new class of ashless dispersants comprising functionalised and/or derivatised olefin polymers based on polymers synthesised using metallocene catalyst systems are described in US-A-5128056, 5151204, 5200103, 5225092, 5266223, 5334775; WO-A-94/19436, 94/13709; and EP-A-440506, 513157, 513211. These dispersants are described as having superior viscometric properties as expressed in a ratio of CCS viscosity to kV100°C.

It has now been found that certain multigrade crankcase oils formulated 15 with this new class of dispersant may provide better fuel economy and better starting at cold temperatures. More economical multigrade crankcase oils may also be blended with less shear stable VMs for improved economy, with a possibility of employing a wider range of polymers. Oils may be blended having extremely good oil shear stability for the most demanding applications where 20 high performance is required such as in turbocharged engines and racing engines, with reduced mechanical breakdown of the oil.

Accordingly, in one aspect the invention provides a multigrade crankcase lubricating oil composition having an initial (unsheared) kV100°C of not more than 1.5 mm 2 /s above the minimum kV100°C for its SAE J300 grade, a final (after shear) kV100°C meeting the minimum kV100°C requirement for its SAE J300 grade and a oil shear stability of less than 15% as measured in the Kurt- Orbahn Diesel Fuel Injector Test (CEC-L-14-A-88), which oil composition comprises: basestock oil; a detergent inhibitor package of lubricating oil additives, which package, when substantially free of additives derived from a polymer having an Mn of greater than 7000, contributes at least 4.5 mm 2 /s of the initial kV100°C of the

I

I lubricating oil and includes an ashless dispersant comprising an oil soluble polymeric hydrocarbon backbone having functional groups in which the hydrocarbon backbone is derived from an ethylene alpha-olefin (EAO) copolymer or alpha-olefin homo- or copolymer having an Mn of from 500 to 1000, and a viscosity modifier comprising one or more polymeric additives having an Mn of greater than 20,000.

Preferably the oil has an initial (unsheared) kV100°C of not more than 1.25 mm 2 more preferably 1mm 2 above the minimum high temperature viscosity for the SAE J300 grade, and desirably has an oil shear stability of less than 10%, preferably less than more preferably less than 1.75%, still more preferably less than 1% and most preferably less than as measured in the Kurt-Orbahn test. The detergent inhibitor package preferably contributes at least 5mm 2 more preferably at least 6mm 2 /s of the initial kV100°C of the lubricating 15 oil.

The detergent inhibitor package contribution to the initial kV100°C of the lubricating oil can be determined by blending oils with and without the package and measuring the difference in kV100°C. This kV100°C contribution excludes the contribution of any long chain polymer materials, which are normally 20 introduced only as the separate VM component or other long chain additives such as pour point depressants introduced with the VM. In the event that such a pour point depressant is included in the detergent package, its contribution to kV 100°C is not included as the detergent inhibitor package contribution.

Preferably the ethylene alpha-olefin (EAO) copolymer or alpha-olefin homo-or copolymer is one having >30% of terminal vinylidene unsaturation.

The invention also extends to the use in a multigrade crankcase oil of an ashless dispersant comprising an oil soluble polymeric hydrocarbon backbone having functional groups in which the hydrocarbon backbone is derived from an ethylene alpha-olefin (EAO) copolymer or alpha-olefin homo-or copolymer preferably having >30% of terminal vinylidene unsaturation and an Mn of from 500 to 7000, to improve the fuel economy performance of the oil. The invention further provides a process for improving the fuel economy of a gasoline or diesel I 6 engine in which the engine is lubricated with a multigrade crankcase oil which contains an ashless dispersant comprising an oil soluble polymeric hydrocarbon backbone having functional groups, in which the hydrocarbon backbone is derived from an ethylene alpha-olefin (EAO) copolymer or alphaolefin homo- or copolymer preferably having >30% of terminal vinylidene unsaturation and an Mn of from 500 to 7000.

The fuel economy benefit may be achieved according to the invention even when using relatively less shear stable VMs having an SSI of 30 or

S

S

S S e e o WO 95/34617 PCT/EP95/02270 .7 greater, though by using VMs with greater shear stability, of less than 30 SSI, fuel economy benefits may be achieved in an oil with good oil shear stability.

The invention may provide a means of achieving adequate fuel economy performance in the ASTM Sequence VIA engine test for the ILSAC GGF-2 oil specification.

DETAILED DESCRIPTION A. BASESTOCK The basestock used in the lubricating oil may be selected from any of the synthetic or natural oils used as crankcase lubricating oils for sparkignited and compression-ignited engines. The lubricating oil base stock conveniently has a viscosity of about 2.5 to about 12 mm 2 /s and preferably about 2.5 to about 9 mm 2 /s at 100oC. Mixtures of synthetic and natural base oils may be used if desired.

B. ASHLESS DISPERSANT The ashless dispersant comprises 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 dispersant 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 polyalkylene polyamine.

The oil soluble polymeric hydrocarbon backbone used in an ashless dispersants in the detergent inhibitor package is selected from ethylene alpha-olefin (EAO) copolymers and alpha-olefin homo- and copolymers such as may be prepared using the new metallocene catalyst chemistry, which may have a high degree of terminal vinylidene unsaturation. The term alpha-olefin is used herein to refer to an olefin of the formula: WO 95/34617 PCT/EP95/02270 8

R'

H- C CH2 wherein R' is preferably a C 1

C

1 8 alkyl group. The requirement for terminal vinylidene unsaturation refers to the presence in the polymer of the following structure:

R

Poly- C =-CH2 wherein Poly is the polymer chain and R is typically a C 1

C

1 8 alkyl group, typically methyl or ethyl. Preferably the polymers will have at least and most preferably at least 60%, of the polymer chains with terminal vinylidene unsaturation. As indicated in WO-A-94/19426, ethylene/1-butene copolymers typically have vinyl groups terminating no more than about percent of the chains, and internal mono-unsaturation in the balance of the chains. The nature of the unsaturation may be determined by FTIR spectroscopic analysis, titration or C-13 NMR.

The oil soluble polymeric hydrocarbon backbone may be a homopolymer polypropylene) or a copolymer of two or more of such olefins copolymers of ethylene and an alpha-olefin such as propylene or butylene, or copolymers of two different alpha-olefins). Other copolymers include those in which a minor molar amount of the copolymer monomers, 1 to 10 mole is an a,c-diene, such as a C 3 to C 22 non-conjugated diolefin a copolymer of isobutylene and butadiene, or a copolymer of ethylene, propylene and 1,4-hexadiene or 5-ethylidene-2-norbornene).

Atactic propylene oligomer typically having M, of from 700 to 5000 may also be used, as described in EP-A-490454, as well as heteropolymers such as polyepoxides.

One preferred class of olefin polymers is polybutenes and specifically poly-n-butenes, such as may be prepared by polymerization of a C4 refinery stream. Other preferred classes of olefin polymers are EAO copolymers that preferably contain 1 to 50 mole% ethylene, and more preferably 5 to 48 mole% ethylene. Such polymers may contain more than one alpha-olefin and may contain one or more C 3 to C22 diolefins. Also usable are mixtures of EAO's of varying ethylene content. Different polymer types, EAO, may WO 95/34617 PCT/EP95/02270 9 also be mixed or blended, as well as polymers differing in M; components derived from these also may be mixed or blended.

The olefin polymers and copolymers preferably have an M of from 700 to 5000, more preferably 2000 to 5000. Polymer molecular weight, specifically Mn, can be determined by various known techniques. One convenient method is gel permeation chromatography (GPC), which additionally provides molecular weight distribution information (see W. W.

Yau, J. J. Kirkland and D. D. Bly, "Modern Size Exclusion Liquid Chromatography", John Wiley and Sons, New York, 1979). Another useful method, particularly for lower molecular weight polymers, is vapor pressure osmometry (see, ASTM D3592).

The degree of polymerisation Dp of a polymer is: Mn x mol.% monomer i 100 x mol.wt monomer i i and thus for the copolymers of two monomers Dp may be calculated as follows: Mn x mol.% monomer 1 Mn x mol.% monomer 2 p 100 x mol.wt monomer 1 100 x mol.wt monomer 2 In a preferred aspect of the invention the degree of polymerisation for the polymer backbones used in the invention is at least 45, typically from to 165, more preferably 55 to 140.

Particularly preferred copolymers are ethylene butene copolymers.

In a preferred aspect of the invention the olefin polymers and copolymers may be prepared by various catalytic polymerization processes using metallocene catalysts which are, for example, bulky ligand transition metal compounds of the formula: [L]mM[A]n where L is a bulky ligand; A is a leaving group, M is a transition metal, and m and n are such that the total ligand valency corresponds to the transition WO 95/34617 PCT/EP95/02270 metal valency. Preferably the catalyst is four co-ordinate such that the compound is ionizable to a 1+ valency state.

The ligands L and A may be bridged to each other, and if two ligands A and/or L are present, they may be bridged. The metallocene compound may be a full sandwich compound having two or more ligands L which may be cyclopentadienyl ligands or cyclopentadienyl derived ligands, or they may be half saindwich compounds having one such ligand L. The ligand may be mono- or polynuclear or any other ligand capable of rn-5 bonding to the transition metal.

One or more of the ligands nay 7t-bond to the transition metal atom, which may be Group 4, 5 or 6 transition metal and/or a lanthanide or actinide transition metal, with zirconium, titanium and hafnium being particularly preferred.

The ligands may be substituted or unsubstituted, and mono-, di-, tri, tetra- and penta-substitution of the cyclopentadienyl ring is possible.

Optionally the substituent(s) may act as one or more bridges between the ligands and/or leaving groups and/or transition metal. Such bridges typically comprise one o more of a carbon, germanium, silicon, phosphorus or nitrogen atom-containing radical, and preferably the bridge places a one atom link between the entities being bridged, although that atom may and often does carry other substituents.

The metallocene may also contain a further displaceable ligand, preferably displaced by a cocatalyst a leaving group that is usually selected from a wide variety of hydrocarbyl groups and halogens.

Such polymerizations, catalysts, and cocatalysts or activators are described, for example, in US-A-4530914, 4665208, 4808561, 4871705, 4897455, 4937299, 4952716, 5017714, 5055438, 5057475, 5064802, 5096867, 5120867, 5124418, 5153157, 5198401, 5227440, 5241025; EP-A- 129368, 277003, 277004, 420436, 520732; and WO-A-91/04257, 92/00333, 93/08199, 93/08221, 94/07928 and 94/13715.

The oil soluble polymeric hydrocarbon backbone may be functionalized to incorporate a functional group into the backbone of the polymer, or as one or more groups pendant from the polymer backbone. The functional group typically will be polar and contain one or more hetero atoms WO 95/34617 PCT/EP95/02270 11 such as P, 0, S, N, halogen, or boron. It can be attached to a saturated hydrocarbon part of the oil soluble polymeric hydrocarbon backbone via substitution reactions or to an olefinic portion via addition or cycloaddition reactions. Alternatively, the functional group can be incorporated into the polymer in conjunction with oxidation or cleavage of the polymer chain end as in ozonolysis).

Useful functionalization reactions include: halogenation of the polymer at an olefinic bond and subsequent reaction of the halogenated polymer with an ethylenically unsaturated functional compound maleation where the io polymer is reacted with maleic acid or anhydride); reaction of the polymer with an unsaturated functional compound by the "ene" reaction absent halogenation; reaction of the polymer with at least one phenol group (this permits derivatization in a Mannich base-type condensation); reaction of the polymer at a point of unsaturation with carbon monoxide using a Koch-type reaction to introduce a carbonyl group in an iso or neo position; reaction of the polymer with the functionalizing compound by free radical addition using a free radical catalyst; reaction with a thiocarboxylic acid derivative; and reaction of the polymer by air oxidation methods, epoxidation, chloroamination, or ozonolysis.

The functionalized oil soluble polymeric hydrocarbon backbone is then further derivatized with a nucleophilic reactant such as an amine, aminoalcohol, alcohol, metal compound or mixture thereof to form a corresponding derivative. Useful amine compounds for derivatizing functionalized polymers comprise at least one amine and can comprise one or more additional amine or other reactive or polar groups. These amines may be hydrocarbyl amines or may be predominantly hydrocarbyl amines in which the hydrocarbyl group includes other groups, hydroxy groups, alkoxy groups, amide groups, nitriles, imidazoline groups, and the like. Particularly useful amine compounds include mono- and polyamines, e.g. polyalkylene and polyoxyalkylene polyamines of about 2 to 60, conveniently 2 to 40 3 to total carbon atoms and about 1 to 12, conveniently 3 to 12, and preferably 3 to 9 nitrogen atoms in the molecule. Mixtures of amine compounds may advantageously be used such as those prepared by reaction of alkylene dihalide with ammonia. Preferred amines are aliphatic saturated amines, including, 1,2-diaminoethane; 1,3-diaminopropane; 1,4diaminobutane; 1,6-diaminohexane; polyethylene amines such as diethylene WO 95/34617 PCTIEP95/02270 12 triamine; triethylene tetramine; tetraethyles pentamine; and polypropyleneamines such as 1,2-propylene diamine; and di-(1,2propylene)triamine.

Other useful amine compounds include: alicyclic diamines such as 1,4-di(aminomethyl) cyclohexane, and heterocyclic nitrogen compounds such as imidazolines. A particularly useful class of amines are the polyamido and related amido-amines as disclosed in US 4,857,217; 4,956,107; 4,963,275; and 5,229,022. Also usable is tris(hydroxymethyl)amino methane (THAM) as described in US 4,102,798; 4,113,639; 4,116,876; and UK 989,409.

Dendrimars, star-like amines, and comb-structure amines may also be used.

Similarly, one may use the condensed amines disclosed in US 5,053,152.

The functionalized polymer is reacted with the amine compound according to conventional techniques as described in EP-A 208,560; US 4,234,435 and US 5,229,022.

The functionalized oil soluble polymeric hydrocarbon backbones also may be derivatized with hydroxy compounds such as monohydric and polyhydric alcohols or with aromatic compounds such as phenols and naphthols. Polyhydric alcohols are preferred, alkylene glycols in which the alkylene radical contains from 2 to 8 carbon atoms, Other useful polyhydric alcohols include glycerol, mono-oleate of glycerol, monostearate of glycerol, monomethyl ether of glycerol, pentaerythritol, dipentaerythritol, and mixtures thereof. An ester dispersant may also be derived from unsaturated alcohols such as allyl alcohol, cinnamyl alcohol, propargyl alcohol, 1-cyclohexane-3-ol, and oleyl alcohol. Still other classes of the alcohols capable of yielding ashless dispersants comprise the ether-alcohols and including, for example, the oxy-alkylene, oxy-arylene. They are exemplified by ether-alcohols having up to 150 oxy-alkylene radicals in which the alkylene radical contains from 1 to 8 carbon atoms. The ester dispersants may be di-esters of succinic acids or acidic esters, partially esterified succinic acids; as well as partially esterified polyhydric alcohols or phenols, esters having free alcohols or phenolic hydroxyl radicals. An ester dispersant may be prepared by one of several known methods as illustrated, for example, in US 3,381,022.

A preferred group of ashless dispersants includes those substituted with succinic anhydride groups and reacted with polyethylene amines tetraethylene pentamine), aminoalcohols such as trismethylolaminomethane WO 95/34617 PCT/EP95/02270 13 and optionally additional reactants such as alcohols and reactive metals e.g., pentaerythritol, and combinations thereof). Also useful are dispersants wherein a polyamine is attached directly to the backbone by the methods shown in US 3,275,554 and 3,565,804 where a halogen group on a halogenated hydrocarbon is displaced with various alkylene polyamines.

Another class of ashless dispersants comprises Mannich base condensation products. Generally, these are.prepared by condensing about one mole of an alkyl-substituted mono- or polyhydroxy benzene with about 1 to 2.5 moles of carbonyl compounds formaldehyde and paraformaldehyde) and about 0.5 to 2 moles polyalkylene polyamine as disclosed, for example, in US 3,442,808. Such Mannich condensation products may include a polymer product of a metallocene cataylsed polymerisation as a substituent on the benzene group or may be reacted with a compound containing such a polymer substituted on a succinic anhydride, in a mannersimilar to that shown in US 3,442,808.

Examples of functionalized and/or derivatized olefin polymers based on polymers synthesized using metallocene catalyst systems are described in publications identified above.

The dispersant can be further post-treated by a variety of conventional post treatments such as boration, as generally taught in US 3,087,936 and 3,254,025. This is readily accomplished by treating an acyl nitrogencontaining dispersant with a boron compound selected from the group consisting of boron oxide, boron halides, boron acids and esters of boron acids, in an amount to provide from about 0.1 atomic proportion of boron for each mole of the acylated nitrogen composition to about 20 atomic proportions of boron for each atomic proportion of nitrogen of the acylated nitrogen composition. Usefully the dispersants contain from about 0.05 to wt. e.g. 0.05 to 0.7 wt. boron based on the total weight of the borated acyl nitrogen compound. The boron, which appears be in the product as dehydrated boric acid polymers (primarily (HBO 2 3 is believed to attach to the dispersant imides and diimides as amine salts the metaborate salt of the diimide. Boration is readily carried out by adding from about 0.05 to 4, 1 to 3 wt. (based on the weight of acyl nitrogen compound) of a boron compound, preferably boric acid, usually as a slurry, to the acyl nitrogen compound and heating with stirring at from 1350 to 1900 C, 140°-1700 C, for from 1 to 5 hours followed by nitrogen stripping. Alternatively, the boron WO 95/34617 PCT/EP95/02270 14 treatment can be carried out by adding boric acid to a hot reaction mixture of the dicarboxylic acid material and amine while removing water.

C. VISCOSITY MODIFIERS The viscosity modifier used in the invention functions 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 0o also known and may be prepared as described above for ashless dispersants. The oil soluble polymeric hydrocarbon backbone will usually have a Mn of from 20,000, more typically from 20,000 up to 500,000 or greater. In general, these dispersant viscosity modifiers are functionalized polymers inter polymers of ethylene-propylene post grafted with an active monomer such as maleic anhydride) which are then derivatized with, for example, an alcohol or amine.

Suitable compounds for use as monofunctional viscosity modifiers are generally high molecular weight hydrocarbon polymers, including polyesters.

Oil soluble viscosity modifying polymers generally have weight average molecular weights of from about 10,000 to 1,000,000, preferably 20,000 to 500,000, which may be determined by gel permeation chromatography (as described above) or by light scattering.

Representative examples of suitable viscosity modifiers are polyisobutylene, copolymers of ethylene and propylene and higher alphaolefins, 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.

In the first aspect of the invention the viscosity modifier can be chosen from any of the above categories of additive in such an amount to obtain the multigrade viscosity requirements within the additional constraints of the invention. In the oils of the second aspect of the invention the viscosity

I

WO 95/34617 PfTiEP95/02270 modifier has a relatively high SSI, and is preferably a polyisobutylene or copolymer of ethylene and propylene or higher alpha-olefin, as such viscosity modifiers are particularly economic and effective. In the third aspect of the invention the oils having a particularly high shear stability are preferably blended with a highly shear stable viscosity modifier having an SSI of 5 or less and such viscosity modifiers include in particular hydrogenated polyisoprene star polymers and hydrogenated styrene-isoprene block copolymers. An example of commercially available viscosity modifers of this type is the family of products sold by Shell International Chemical Co. Limited l0 as their Shellvis T M 200 series..

The viscosity modifier used in any aspect of the invention will be used in an amount to give the required viscosity characteristics. Since they are typically used in the form of oil solutions the amount of additive employed will depend on the concentration of polymer in the oil solution comprising the additive. However by way of illustration, typical oli solutions of polymer used as VMs are used in amount of from 1 to 30% of the blended oil. The amount of VM as active ingredient of the oil is generally from 0.01 to 6 wt%, and more preferably from 0.1 to 2 wt%.

OTHER DETERGENT INHIBITOR PACKAGE ADDITIVES Additional additives are typically incorporated into the compositions of the present invention. Examples of such additives are metal or ashcontaining detergents, antioxidants, anti-wear agents, friction modifiers, rust inhibitors, anti-foaming agents, demulsifiers, and pour point depressants.

Metal-containing or ash-forming detergents function both as detergents to reduce or remove deposits and as acid neutralizers or rust inhibitors, thereby reducing wear and corrosion and extending engine life.

Detergents generally comprise a polar head with a long hydrophobic tail, with the polar head comprising a metal salt of an acidic organic compound. The salts may contain a substantially stoichiometric amount of the metal in which case they are usually described as normal or neutral salts, and would typically have a total base number or TBN (as may be measured by ASTM D2896) of from 0 to 80. It is possible to include large amounts of a metal base by reacting an excess of a metal compound such as an oxide or hydroxide with an acidic gas such as carbon dioxide. The resulting overbased detergent WO 95/34617 PCTIEP95/02270 S16 comprises neutralised detergent as the outer layer of a metal base (e.g.

carbonate) micelle. Such overbased detergents may have a TBN of 150 or greater, and typically of from 250 to 450 or more.

Detergents that may be used include oil-soluble neutral and overbased sulfonates, phenates, sulfurized phenates, thiophosphonates, salicylates, and naphthenates and other oil-soluble carboxylates of a metal, particularly the alkali or alkaline earth metals, 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. Particularly convenient metal detergents are neutral and overbased calcium sulfonates having TBN of from to 450 TBN, and neutral and overbased calcium phenates and sulfurized phenates having TBN of from 50 to 450.

Sulfonates may be prepared from sulfonic acids which are typically obtained by the sulfonation of alkyl substituted aromatic hydrocarbons such as those obtained from the fractionation of petroleum or by the alkylation of aromatic hydrocarbons. Examples included those obtained by alkylating benzene, toluene, xylene, naphthalene, diphenyl or their halogen derivatives such as chlorobenzene, chlorotoluene and chloronaphthalene. The alkylation may be carried out in the presence of a catalyst with alkylating agents having from about 3 to more than 70 carbon atoms. The alkaryl sulfonates usually contain from about 9 to about 80 or more carbon atoms, preferably from about 16 to about 60 carbon atoms per alkyl substituted aromatic moiety.

The oil soluble sulfonates or alkaryl sulfonic acids may be neutralized with oxides, hydroxides, alkoxides, carbonates, carboxylate, sulfides, hydrosulfides, nitrates, borates and ethers of the metal. The amount of metal compound is chosen having regard to the desired TBN of the final product but typically ranges from about 100 to 220 wt (preferably at least 125 wt of that stoichiometrically required.

Metal salts of phenols and sulfurised phenols are prepared by reaction with an appropriate metal compound such as an oxide or hydroxide and neutral or overbased products may be obtained by methods well known in the art. Sulfurised phenols may be prepared by reacting a phenol with sulfur or a WO 95/34617 PCTIEP95/02270 17 sufur containing compound such as hydrogen sulfide, sulfur monohalide or sulfur dihalide, to form products which are generally mixtures of compounds in which 2 or more phenols are bridged by sulfur containing bridges.

Dihydrocarbyl dithiophosphate metal salts are frequently used as antiwear and antioxidant agents. The metal may be an alkali or alkaline earth metal, or aluminum, lead, tin, molybdenum, manganese, nickel or copper.

The zinc salts are most commonly used in lubricating oil in amounts of 0.1 to preferably 0.2 to 2 wt. based upon the total weight of the lubricating oil composition. They may be prepared in accordance with known techniques by first forming a dihydrocarbyl dithiophosphoric acid (DDPA), usually by reaction of one or more alcohol or a phenol with P 2

S

5 and then neutralizing the formed DDPA with a zinc compound. For example, a dithiophosphoric acid may be made by reacting mixtures of primary and secondary alcohols.

Alternatively, multiple dithiophosphoric acids can be prepared where the hydrocarbyl groups on one are entirely secondary in character and the hydrocarbyl groups on the others are entirely primary in character. To make the zinc salt any basic or neutral zinc compound could be used but the oxides, hydroxides and carbonates are most generally employed.

Commercial additives frequently contain an excess of zinc due to use of an excess of the basic zinc compound in the neutralization reaction.

The preferred zinc dihydrocarbyl dithiophosphates are oil soluble salts of dihydrocarbyl dithiophosphoric acids and may be represented by the following formula: s RO\11 R' p-s Zn

R

2 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, ipropyl, n-butyl, i-butyl, sec-butyl, amyl, n-hexyl, i-hexyl, n-octyl, decyl, dodecyl, octadecyl, 2-ethylhexyl, phenyl, butylphenyl, cyclohexyl, methylcyclopentyl, propenyl, butenyl. In order to obtain oil solubility, the total number of carbon atoms R and in the dithiophosphoric acid will I WO 95/34617 PCT/EP95/02270 18 generally be about 5 or greater. The zinc dihydrocarbyl dithiophosphate can therefore comprise zinc dialkyl dithiophosphates. Conveniently at least (mole) of the alcohols used to introduce hydrocarbyl groups into the dithiophosphoric acids are secondary alcohols.

Oxidation inhibitors or antioxidants reduce the tendency of mineral oils to deteriorate in service which deterioration can be evidenced by the products of oxidation such as sludge and varnish-like deposits on the metal surfaces and by viscosity growth. Such oxidation inhibitors include hindered phenols, to alkaline earth metal salts of alkylphenolthioesters having preferably C 5 to

C

12 alkyl side chains, calcium nonylphenol sulfide, ashless oil soluble phenates and sulfurized phenates, phosphosulfurized or sulfurized hydrocarbons, phosphorous esters, metal thiocarbamates, oil soluble copper compounds as described in US 4,867,890, and molybdenum containing compounds.

Typical oil soluble aromatic amines having at least two aromatic groups attached directly to one amine nitrogen contain from 6 to 16 carbon atoms. The amines may contain more than two aromatic groups.

Compounds having a total of at least three aromatic groups in which two aromatic groups are linked by a covalent bond or by an atom or group an oxygen or sulfur atom, or a -SO2- or alkylene group) and two are directly attached to one amine nitrogen also considered aromatic amines.

The aromatic rings are typically substituted by one or more substituents selected from alkyl, cycloalkyl, alkoxy, aryloxy, acyl, acylamino, hydroxy, and nitro groups.

Friction modifiers may be included to improve fuel economy. Oilsoluble alkoxylated mono- and diamines are well known to improve boundary layer lubrication. The amines may be used as such or in the form of an adduct or reaction product with a boron compound such as a boric oxide, boron halide, metaborate, boric acid or a mono-, di- or trialkyl borate.

Other friction modifiers are known, Among these are esters formed by reacting carboxylic acids and anhydrides with alkanols. Other conventional friction modifiers generally consist of a polar terminal group carboxyl or hydroxyl) covalently bonded to an oleophillic hydrocarbon chain. Esters of carboxylic acids and anhydrides with alkanols are described in US 4,702,850.

WO 95/34617 PCT/EP95/02270 19 Examples of other conventional friction modifiers are described by M. Belzer in the "Journal of Tribology" (1992), Vol. 114, pp. 675-682 and M. Belzer and S. Jahanmir in "Lubrication Science" (1988), Vol. 1, pp. 3-26.

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 0o typically not required with the formulation of the present invention. Typically such compounds are the thiadiazole polysulfides containing from 5 to carbon atoms, their derivatives and polymers thereof. Derivatives of 1,3,4 thiadiazoles such as those described in U.S. Pat. Nos. 2,719,125; 2,719,126; and 3,087,932; are typical. Other similar materials are described in U.S. Pat.

Nos. 3,821,236; 3,904,537; 4,097,387; 4,107,059; 4,136,043; 4,188,299; and 4,193,882. Other additives are the thio and polythio sulfenamides of thiadiazoles such as those described in UK. Patent Specification No.

1,560,830. Benzotriazoles derivatives also fall within this class of additives.

When these compounds are included in the lubricating composition, they are preferrably present in an amount not exceding 0.2 wt active ingredient.

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 bisepoxide with a polyhydric alcohol. The demulsifier should be used at a level not exceeding 0.1 mass active ingredient. A treat rate of 0.001 to 0.05 mass active ingredient is convenient.

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 C 8 to C 1 8 dialkyl fumarate/vinyl acetate copolymers and polyalkylmethacrylates.

Foam control can be provided by many compounds including an antifoamant of the polysiloxane type, for example, silicone oil or polydimethyl siloxane.

WO 95/34617 PCT/EP95/02270 Some of the above-mentioned additives can provide a multiplicity of effects; thus for example, a single additive may act as a dispersant-oxidation inhibitor. This approach is well known and does not require further elaboration.

When lubricating compositions contain one or more of the abovementioned additives, each additive is typically blended into the base oil in an amount which enables the additive to provide its desired function.

Representative effective amounts of such additives, when used in crankcase lubricants, are listed below. All the values listed are stated as mass percent active ingredient.

ADDITIVE MASS MASS (Broad) (Preferred) Ashless Dispersant 0.1 -20 1 -8 Metal detergents 0.1 15 0.2-9 Corrosion Inhibitor 0 5 0 Metal dihydrocarbyl dithiophosphate 0.1 -6 0.1 -4 Supplemental anti-oxidant 0 -5 0.01 Pour Point Depressant 0.01 -5 0.01- Anti-Foaming Agent 0 5 0.001-0.15 Supplemental Anti-wear Agents 0 0.5 0 0.2 Friction Modifier 0 5 0 Viscosity Modifier 1 0.01-6 0 -4 Mineral or Synthetic Base Oil Balance Balance 1. Subject to the limitations of the lubricating oils of the invention The components may be incorporated into a base oil in any convenient way. Thus, each of the components can be added directly to the oil by dispersing or dissolving it in the oil at the desired level of concentration.

Such blending may occur at ambient temperature or at an elevated temperature.

Preferably all the additives except for the viscosity modifier and the pour point depressant are blended into a concentrate or additive package described herein as the detergent inhibitor package, that is subsequently blended into basestock to make finished lubricant. Use of such concentrates WO 95/34617 PCT/EP95/02270 21 is conventional. The concentrate will typically be formulated to contain the additive(s) in proper amounts to provide the desired concentration in the final formulation when the concentrate is combined with a predetermined amount of base lubricant.

Preferably the concentrate is made in accordance with the method described in US 4,938,880. That patent describes making a premix of ashless dispersant and metal detergents that is pre-blended at a temperature of at least about 100C. Thereafter the pre-mix is cooled to at least 85 0 C and the additional components are added.

The final formulations may employ from 2 to 15 mass and preferably to 10 mass typically about 7 to 8 mass of the concentrate or additive package with the remainder being base oil.

The invention will now be described by of illustration only with reference to the following examples. In the examples, unless otherwise noted, all treat rates of all additives are reported as mass percent active ingredient.

Examples Examples 1-5 and Comparative Example 1 A series of 15W/40 multigrade crankcase lubricating oils meeting API SH/CD specifications were prepared from a mineral basestock, a detergent inhibitor package (DI package) containing an ashless dispersant, ZDDP, antioxidant, metal-containing detergents, friction modifier, demulsifier and an antifoam agent, and a separate viscosity modifier which is an oil solution of an ethylene-propylene copolymer having 25SSI, used at various treat rates.

Comparative Example 1 used a conventional borated polyisobutenyl succinimide dispersant (PIBSA/PAM), whereas Examples 1-4 used various ashless dispersants having an ethylene/butene copolymer backbone, functionalised by the introduction of a carbonyl group by the Koch reaction which is in turn reacted with a polyamine and borated (EBCO/PAM). The preparation of such an ashless dispersant is described in WO-A-94/13709.

The various ashless dispersants were used at different treat rates. The kV100 °C viscosity for each oil was measured and then the Kurt-Orbahn test was WO 95/34617 PCT/EP95/02270 22 conducted to determine the oil shear stability. The results are shown in the following table, Table 1: WO 95/34617 PCT/EP95/02270 23 Table 1 Example Comp. 1 1 2 3 4 type PIBSA/PAM EBCO/PAM EBCO/PAM EBCOIPAM EBCO/PAM EBCO/PAM treat 3.0 3.0 2.1 2.4 3.0 Polymer Mn (GPC) 2225 3700 4700 2400 2750 3250 Dp _39 93 127 60 74 Terminal 61 64 64 69 66 vinylidene C, (mole%) 0 41 51 39 50 46

VM

treat 7.2 2.5 4.5 6.0 2.5 kV100°C (mm 2 1s) Oil (initial) 13.9 13.8 14.0 13.6 12.6 14.0 DI pack 4 8.6 11.5 4.5 7.8 6.4 contribution Oil (after 12.4 13.1 13.0 12.5 12.1 13.1 shear) loss 10.9 5.3 7.1 8.3 3.4 6.8 Comparative Example 1 shows that with a conventional PIBSA/PAM dispersant an olefin copolymer VM with SSI of 25 requires the oil to be blended to an initial kV100°C of greater than 14 mm 2 /s to ensure that the after shear viscosity is greater than 12.5 mm2/s. Example 1 shows that using the same dispersant treat rate but with the EBCO/PAM dispersant in combination with a greatly reduced amount of VM, according to the invention to an excellent oil shear stability is obtained. The results indicate that a further reduction in the amount of the VM and thus of the initial kV100°C would be possible, which results enables oils with greatly improved fuel economy to be obtained. Example 1 also shows that despite the dispersant being prepared from a polymer of higher Mn than Comparative Example 1 the shear stability of the resulting oil can be improved. Example 1 meets the requirements for SAE 40 grade after shear. Examples 2, 3 and 5 are further examples of oils WO 95/34617 PCTIEP95/02270 24 meeting the 40 grade requirement after shear with high shear stability, with a number of different dispersants.

Example 4 is an oil with extremely good oil shear stability which is close to the 40 grade viscosity limit prior to shear, and loses only 3.4% of its kV100°C during shear in the Kurt-Orbahn test. A small increase in the quantity of VM would enable this oil to meet the SAE 40 grade viscosity limit after shear without raising the initial viscosity as high as 14 mm 2 /s as in Comparative Example 1.

Comparative Example 1 and Example 5 were tested in the Sequence VE engine test (ASTM STP 315) which measures inter alia the dispersancy characteristics of the oil, and thus the effectiveness of the dispersant system within it. The key measurements are sludge and varnish control. A pass in the VE engine for the purposes of achieving API SH performance is a rating of or betteron sludge and 5.0 or better on varnish. The results obtained are given in the following table, Table 2: Table 2 Example VE sludge ratin VE varnish rating Comp. 1 8.8 9.4 6.3 Pass 9.0 These results show that the oils of the invention have excellent disersancy despite the relatively low levels of ashless dispersant whereas the oil of Comparative Example 1 does not pass the VE test on either sludge or varnish rating.

Example 6 Very high oil shear stability oil A 10W/40 multigrade crankcase lubricating oil was blended from a mineral basestock, a hydrocracked mineral basestock, a detergent inhibitor package (DI package) containing an ashless dispersant, ZDDP, antioxidant, metal-containing detergents, friction modifier, demulsifier and an antifoam agent, and a separate viscosity modifier which is an oil solution of a WO 95/34617 PCT/E P95/02270 hydrogenated polyisoprene star Polymer available from Shell International Chemical Co. Limited as ShellvisThI 201. The W~ 00 0 C viscosity for the oil was measured and then the Kurt-Qrbahn test was conducted to determine the oil shear stability. The results are shown in the following table, Table 3: Table 3 Example 6 Dispersant type EBCOIPAM treat Polymer Mn (GPC) 2400 DP Terminal 64 viyideneA~ Cq, mole% 39 VM trea (mm 2 Oil (initial) 14.3 Dl pack (calculated) 1 Oil (after shear) 14.1 ,%Ioss 1.7 Footnote: 1. kWl 00C of Dl pack in Ex. 6 Is calculated as described in the footnote to Table 1.

Claims (18)

1. A multigrade crankcase lubricating oil composition having an initial (unsheared) kV100C of not more than 1.5mm 2 /s above the minimum kV100°C for its SAE J300 grade, a final (after shear) kV100°C meeting the minimum kV100C requirement for its SAE J300 grade and an oil shear stability of less than 15% as measured in the Kurt-Orbahn Diesel Fuel Injector Test (CEC-L-14- A-88) which oil composition comprises: basestock oil, a detergent inhibitor package of lubricating oil additives, which package, when substantially free of additives derived from a polymer having a in of greater than 7000, contributes at least 4.5mm 2 /s of the initial kV100°C of the lubricating oil and includes an ashless dispersant comprising an oil soluble polymeric hydrocarbon backbone having functional groups in which the hydrocarbon backbone is derived from an ethylene alpha-olefin (EAO) copolymer or alpha-olefin homo- or copolymer having an I n of from 500 to 7000, and a viscosity modifier comprising one or more polymeric additives having an Mn of greater than 20,000. B

2. An oil composition as claimed in claim 1, which has an initial kV100°C of not more than 1.25mm 2 /s above the minimum high temperature viscosity for the SAE J300 grade.

3. An oil composition as claimed in claim 2, which has an initial kV100°C of not more than lmm 2 /s above the minimum high temperature viscosity for the SAE J300 grade. I I I r 27

4. An oil composition as claimed in any of claims 1 to 3, which has an oil shear stability of less than 10% as measured in the Kurt-Orbahn test. An oil composition as claimed in claim 4, which has an oil shear stability of less than 8%.

6. An oil composition as claimed in any of claims 1 to 5 in which the detergent inhibitor package contributes at least 5mm 2 /s of the initial kV100°C of the lubricating oil.

7. An oil composition as claimed in claim 6, in which the detergent inhibitor package contributes at least 6mm 2 /s of the initial kV100°C of the lubricating oil.

8. An oil composition as claimed in any of the preceding claims wherein the viscosity modifier has a shear stability index of greater than

9. An oil composition as claimed in claim 8, in which the viscosity modifier has a shear stability index of greater than An oil composition as claimed in claim 8, in which the viscosity modifier has a shear stability index of at least 0

11. An oil composition as claimed in any one of the preceding claims having an oil shear stability of less than 1.75% as measured in the Kurt-Orbahn test.

12. An oil composition as claimed in claim 11, which has an oil shear stability of less than 1%.

13. An oil composition as claimed in claim 12, which has an oil shear stability of less than -r I 1

14. An oil composition as claimed ij any one of the preceding claims, in which the hydrocarbon backbone of the ashiess dispersant is derived from a polymerisation using a metallocene catalyst. An oil composition as claimed in any one of the preceding claims, in which the hydrocarbon backbone of the ashless dispersant is derived from an ethylene alpha-olefin (EAO) copolymer which has an Mn of from 2000 to 5000.

16. An oil composition as claimed in any one of the preceding claims, in which the hydrocarbon backbone of the ashless dispersant has a degree of polymerisation of a least

17. An oil composition as claimed in claim 16, in which the polymeric hydrocarbon backbone has a degree of polymerisation of from 50 to 165.

18. An oil composition as claimed in any one of the preceding claims in which the ethylene alpha-olefin (EAO) copolymer or alpha-olefin homo-or copolymer is one having >30% of terminal vinylidene unsaturation. .19. The use of a multigrade crankcase oil composition as claimed in cny of claims 1 to 18 for improving the fuel economy performance of the oil in a gasoline or diesel engine. a 9 29 A process for improving the fuel economy of a gasoline or diesel engine in which the engine is lubricated with a multigrade crankcase oil as claimed in any of claims 1 to 18. DATED this 2nd day of February, 1998 EXXON CHEMICAL LIMITED and EXXON CHEMICAL PATENTS INC WATERMARK PATENT TRADEMARK ATTORNEYS 4TH FLOOR, "DURACK CENTRE" 263 ADELAIDE TERRACE PERTH W.A. 6000 AUSTRALIA Ob 0 0 0,* 0 0 0 0* 0* 0 0 *000 0* g INTERNATIONAL SEARCH REPORT Intern at Application No PCT/EP 95/02270 A. CLASSIFICATION OF SUBJECT MATTER IPC 6 C10M161/00 //(C10M161/00,129:95,133:52,143:00),C10N20:02,30:04, 40:25 According to International Patent Classification (IPC) or to both natonal classification and IPC B. FIELDS SEARCHED Minimum documentation searched (classificaton system followed by classification symbols) IPC 6 C10M C08F Documentation searched other than mirmuum documentation to the extent that such documents are included in the fields searched Electronic data base consulted dunng the international search (name of data base and, where practical, search terms used) C. DOCUMENTS CONSIDERED TO BE RELEVANT Category" Citation of document, with imdication, where appropnate, of the relevant passages Relevant to claim No. Y US,A,5 229 022 (W.R.SONG) 20 July 1993 1-18 cited in the application see column 56, line 61 column 57, line 33 see column 5, line 20 column 6, line 56 X 19,20 see column 4, line 30 line 56 see column 69 column 71; example 28 Y US,A,5 200 103 (W.R.SONG) 6 April 1993 1-18 cited in the application see column 29, line 8 line see column 3, line 31 column 4, line 41 see column 2, line 39 line 63 X 19,20 see column 3, line 24 column 28 SFurther documents are listed in the continuation of box C. [M Patent family members are listed in annex. Special categories of cited documents ST' later document published after the international filing date or priority date and not in conflict with the application but document defining the general state of the art which is not or pnont date tand the pncictple or theory undecang the considered to be of particular relevance invention earlier document but published on or after the international document of particular relevance; the claimed inventon filing date cannot be considered novel or cannot be considered to document which may throw doubts on priority claim(s) or involve an inventive step when the document is taken alone which is cited to establish the publication date of another document of particular relevance; the claimed invention citation or other special reason (as specified) cannot be considered to involve an inventive step when the document referring to an oral disclosure, use, exhibition or document is combined with one or more other such docu- other means ments, such combination being obvious to a person skilled document published prior to the international filing date but m the art. later than the pnority date claimed document member of the same patent family Date of the actual completion of the international search Date of mailing of the interational search report 07 1995 October 1995 1 Name and mailing address of the ISA Authonzed officer European Patent Office, P.B. 5818 Patentlaan 2 NL 2280 HV Rijswijk Tel. (+31-70) 340.2040, Tx. 31 651 epo nl, Rotsaert L Fax: (+31-70) 340-3016 Form PCT/ISA/210 (lecond sheet) (July 1992) page 1. of 2 INTERNATIONAL SEARCH REPORT fnterr al Applicaion No PC1/EP 95/02270 C(Contnuatton) DOCUMENTS CONSIDERED TO BE RELEVANT Category' Citation of document, with indicaton, Where appropnate, of the relevant pasages Relevant to claim No. 225 092 (J.EMERT) 6 July 1993 cited in the application see column 31, line 10 line 50 see column 3, line 56 column 4, line 36 see column 3, line 6 line 23 US,A,4 234 435 (N.A.MEINHARDT) 18 November 1980 cited in the application see column 2, line 15 line 56 see column 51, line 60 column 52, line 16 1-18 19,20 1-18 1-18 US,A,4 036 910 see example I (W.S.ANDERSON) 19 July 1977 FoPr PCT/ISA/210 (continuion of second sheet) (July 1992) page 2 of 2 I ql INIT RNATIONAL SEARCH ,.iforniaton on patent family members REPORT Inter lai Application No PCTEP 95/02270 Patent document Publication IPatent family Publication cited In search report I date Imember(s) Idate US-A-5229022 20-07-93 AU-B- EP-A, B ES-T- W-A- US-A- US-A- US-A- US-A- US-A- U-B- AU-B- A- JP-A- 4052089 0353935 2045444 2099598 9001503 5350532 5435926 5433757 5277833 5266223 635812 7010991 0441548 5005097 05-03-90 07-02-90 16-01-94 11-04-90

22-02-90

27-09-94 25-07-95 18-07-95 11-01-94

30-11-93 01-04-93 24- 10-9 1 14-08-91 14-01-93 US-A-5200103 06-04-93 US-A- OE-D- DE-T- EP-A- JP-A- US-A- US-A- US-A- AU-B- CA-A- EP-A, F6 JP-A- WO-A- US-A- 5017299 69101564 69101564 0440507 4339894 5382698 5433874 5345002 4052089 1329218 0356010 2167396 9001503 5186851 2 1-05-9 1 11-05-94 21-07-94 07-08-91 26-11-92 17-01-95 18-07-95 06-09-94 05-03-90 03-05-94 28-02-90 27-06-90 22-02-90 16-02-93 US-A-5225092 06-07-93 AU-B- 636193 22-04-93 AU-B- 7010791 15-08-91 CN-A- 1053810 14-08-91 EP-A- 0440508 07-08-9 1 JP-A- 4363125 16-12-92 US-A- 5284595 08-02-94 US-A- 5294234 15-03-94 US-A-4234435 18-11-80 NONE Form PCT/ISA/2li (patent family annexl (July 19921 page 1 of 2 INTERNATIONAL SEARCH REPORT In ional Apphicallon No Infornutlof on patent ramly members PCT/EP 95/02270 Patent document Publication IPatent family Publication cited in search report date member(s) date US-A-4036910 19-07-77 BE-A- 759713 02-06-71 OE-A- 2060914 24-06-71 FR-A,B 2070826 17-09-71 GB-A- 1336746 07-11-73 NL-A- 7018020 15-06-71 US-A- 3763044 02-10-73 SE-B- 367648 04-06-74 I Prm PCT/ISA/212 (patent famUy annex) (July 1992) page 2 of 2