CA2019452A1 - Water resistant grease composition - Google Patents

Abstract

ABSTRACT OF THE DISCLOSURE

A grease composition having improved water resistance is disclosed. More specifically, the addition of an ethylene copolymer having an amine functionality to a base grease comprising a lubri-cating oil and a water insoluble thickener results in a grease composition which has enhanced water resistance relative to a grease containing an ethylene copolymer without amine functionality.

Description

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~ 1 --WATER RESISTANT GREASE COMPOSITION
BACKGROUND OF THE INVENTION
1. Field of the Invention This invention relates to a grease compo-sition having improved water resistance.

2. Description of Related Art The use of polymers to impart desirable properties to greases is known and widely practiced by grease manufacturer~ (see E. N. Klemgard, ubri-catina Greases ~1937) and C~ J. Boner, Manufacture and Application of Lubricatina Greases (1954)). For example, oil soluble polymers have been used to increase the viscosity of the lubricating oil in the grease, thereby resulting in a grease having en-hanced structural stability, reduced oil separation, and increased water resistance. However, although these benefits could be obtained without polymers using lubricating oils having high viscosity base-stocks, the resulting d~bit on low temperature mobility (i.e. pumpability) severely limits a non-polymer approach.

In addition, a recent publication (see G. D. ~ussey, "Alternation of ~rease Characteristics with New Generation Polymers", NLGI Spokesman, August 1987) compared the performance of commonly used polymers in various greases. However, none of the compositions mentioned in these references teach or suggest the water resistancs grease composition described hereinafter.

SUMMARY OF TH~ INVENTION

This invention concerns a grease composi-tion having improved water resistance due to the addition of a particular oil soluble ethylene copolymer. More specifically, a grease composition comprising (1) a lubricating oil, (2) a water insoluble thickener, and (3) an ethylene copol~mer having an amine functionality has been found to have enhanced water resistance relative to that obtained i~ the copolymer did not have amine functionality.
A further improvement in water resistance is obtained when lower molecular weight versions of the copolymer are used.

DETAILED DESCRIPTION OF THE INVENTIQN

The essential components of this invention are a lubricating oil, a water insoluble thickener, and an ethylene copolymer having amine function-ality.

A wide variety of lubricating oils can be employed in preparing the grease composition of this invention. Accordingly, the lubricating oil base can be any of the conventionally used mineral oils, synthetic hydrocarbon oils, or synthetic ester oils.
In general, these lubricating oils will have a viscosity in the range of about 5 to about 5,000 cSt at 40C, although typical applications will require an oil having a viscosity ranging from about 25 to about 2,000 cSt at 40~C. Mineral lubricating oil base stocks used in preparing the lubricating composition can be any conventionally refined base 2 ~ 3J

stocks derived from para~finic, naphthenic, and mixed base crudes. Synthetic lubricating oils that can be used include esters of dibasic acids such as di-2-ethylhexyl sebacate, esters of glycols such as a C13 oxo acid diester o~ tetraethylene glycol, or complex esters such as the ester formed from 1 mole of sebacic acid, 2 moles o~ tetraethylene glycol, and 2 moles of 2-ethylhexanoic acid. Other synkhe-tic oils that can be used include synthetic hydro-carbons such as polyalphaolefins; alkyl benzenes (e.~., alkylate bottoms from the alkylation sf benzene with tetrapropylene, or the copolymers of ethylene and propylene silicon oils, e.q., ethyl phenyl polysiloxanes, methyl polysiloxanes, etc.~;
polyglycol oils (e.~., those obtained by condensing butyl alcohol with propylene oxide); and car~onate esters (e.a., the product of reacting Cg oxo alcohol with ethyl carbonate to form a half ester followed by reaction o~ the latter with tetraethylene glycol, etc.). Other suitable synthetic oils include the polyphenyl ethers, e.q., those having from about 3 to 7 ether linkages and about 4 to 8 phenyl groups.
(See U.S. Patent 3,424,678, column 3.) Normally, the lubricating oil will comprise a major amount o~
the grease composition. Typically, the amount of lubricating oil will range from above about 50 to about 90 wt.%, preferably from about 70 to about 85 wt.%, of the grease composition.

The grease composition will also contain a thickener dispersed in the lubricating oil to form a ba~e grease. ~owever, the particular thickener employed is not critical and can vary broadly provided it is essentially water insoluble. For example, the thickener may be based on aluminum, barium, calcium, lithium soaps, or their complexes.
Soap thickeners may be derived from a wide range of animal oils, vegetable oils, and greases as well as the fatty acids derived there~rom. These materials are well known in the art and are described in, for example, C. J. Boner, Manufacture and Application of Lubricatiny Greases, Chapter 4, Robert E~ Xrieger Publishing Company, Inc., New York (1971). Carbon black, silica, and clays may be used as well as dyes, polyureas, and other organic thickeners.
Pyrrolidone based thickeners can also ba used.
Preferred thickeners are based on lithium soap, calcium soap, their complexes, or mixtures thereof.
Particularly preferred is a lithium or lithium complex thickener that incorporates an hydroxy ~atty acid having from 12 to 24 (preferably from 16 to 20) carbon atoms. A preferred hydroxy fatty acid is an hydroxy stearic acid (e.~., a 9-hydroxy or a 10-hydroxy stearic acid) of which 12-hydroxy stearic acid is most preferred (See U.S. Patent 3,929,651, the disclosure of which is incorporated herein by reference). The amount of thickener in the lubri-cating composition will typically range from about 1 to about 15 wt.%. For most purposes, between about 6 to about 12 wt.%, preferably ~etween a~out 8 to abou~ 10 wt.%, of the thickener will be pre~ent in the composition.

The grease composition will also contain an ethylene copolymer having amine functionality.
By "amine functionality" is meant the oil soluble ethylene copolymers d~scribed in U.S. 4,517,104, the disclosure of which is incorporated herein by 2 ~

reference. In general, these oil soluble ethylenP-copolymers will have a number average molecular w~ight (Mn) of from about 5,000 to about 500,000;
preferably from about 10,Q00 to about 300,000, and optimally from about 20,000 to about 175,000. These polymers will generally have a narrow range of molecular weight, as determined by the ratio of weight average molecular weight (Mw) to number average molecular waight (Mn). Polymers having a MW/Mn of less than 10, preferably less than 7, and more preferably 4 or less are most desirable. As used herein (Mn) and (Mw) are measured by the well known techniques of vapor phase osmometry (VPO), membrane osmometry, and gel permeation chromoto-graphy.

These polymers are prepared from ethylene and ethylenically unsaturated hydrocarbons including cyclic, alicyclic and acyclic, containing from 3 to 28 carbonæ, e.~. 2 to 18 carbons. The ethylene copolymers may contain from about 15 to about 90 wt.%, preferably from about 30 to about 80 wt.%, of ethylene and from about 10 to about 85 wt.%, prefer-ably from about 20 to about 70 wt.%, of one or more C3 to C28, preferably r3 to C1g, more preferbly C3 to Cg, alpha olefins. While not essential, such copolymers preferably have a degree o~ crystallinity of less than 25 wt %, as determined by X-ray and differential scanning calorimetry. Copolymers of ethylene and propylene are most preferred. Other alpha-olefins suitable in place of propylene to form the copolymer, or to be used in combination with ethylene and propylene, to form a terpolymer, tetra-polymer, etc., include 1-butene, 1-pentene, 1-2 ~ 2 hexene, 1-heptene, 1-octene, lOnonene, l-decene, etc.; also branched chain alpha-ole~ins such as 4-methyl-1-pentene, 4-methyl-1-hexene, 5-methyl pentene-l, 4,4-dimethyl-1-pentene, and 6~methyl heptene-l, etc., and mixtures thereo~.

The term copolymer as used herein, unless otherwise indicated, includes terpolymers, tetra-polymers, etc., of ethylene, said C3_2g alpha-olefin and/or a non-conjugated diolefin or mixtures of such diolefins which may also he used. The amount of the non-conjugated diolefin will generally range from about 0.5 to 20 mole percent, preferably a~out 1 to about 7 mole percent, based on the total amount of ethylene and alpha-ole~in present.

Representative examples of non-conjugated dienes that may be used as the third monomer in the terpolymer include:

a. Straight chain acyclic dienes such as:
1,4-hexadiene; 1,5-heptadiene; 1,6-octadiene.

b. Branched chain acyclic dienes such as:
5-methyl-1,4-hexadiene; 3,7-dimethyl 1,6-octadiene;

3,7 dimethyl 1,7-octadiene; and the mixed isomers of dihydro-myrcene and dihydro-cymene.

c. Single ring alicyclic-dienes such as:
1,4-cyclohexadiene; 1,5-cyclooctadiene; 1,5-cyclo-dodecadiene; 4-vinylcyclohexene; l-allyl, 4-iso-propylidene cyclohexane; 3-allyl-cyclopentene;

4-allyl cyclohexene and 1-isopropenyl-4-(4-butenyl)-cyclohexane.

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d. Multi-single ring alicyclic dienes such as: 4,4'-dicyclopentenyl and 4,4'-dicyclo-hexenyl dienes.

e. Multi-ring alicyclic fused and bridged ring dienes such as: tetrahydroindene; methyl tetrahydroindene; dicyclopentadiene; bicyclo(2.2.1)-hepta 2,5-diene; alkyl, alkenyl, alkylidene, cyclo-alkenyl and cycloalkylidene norbornenes such as:
ethyl norbornene; 5-methylene~6-methyl~2-norbornene;

5-methylene--6, 6-dimethyl-2-norbornene; 5-propenyl-2-norbornene 5-~3-cyclopentenyl)-2-norbornene and 5-cyclohexylidene-2-norbornene; norbornadiene; etc.

Ethylenically unsaturated carboxylic acid materials which are grafted (attached) onto the ethylene copolymer contain at least one ethylenic bond and at least one, pre~erably two, carboxylic acid groups, or an anhydride group, or a polar group which can be converted into said carboxyl groups by oxidation or hydrolysis. Ma~eic anhydride or a derivative thereof is preferred because it does not appear to homopolymerize appreciably but grafts onto the ethylene copolymer to give two carboxylic acid functionalities. Such preferred materials have the general formula Rl 12 C === ~
o-=l c==o o wherein Rl and R2 are hydrogen or a halogen.
Suitable examples additionally include chloro-maleic anhydride, itaconic anhydride, or the corresponding dicarboxylic acids, such as maleic acid or fumaric acid or their monoesters, etc.

As taught by U.S. Patents 4,160,739 and 4,161,452, various unsaturated comonomers may be grafted on the olefin copolymer together with the unsaturated acid component, e.~. maleic anhydride.
Such graft monomer systems may comprise one or a mixture o~ comonomers di~ferent from the unsaturated acid component and which contain only one copolymer-izable double bond and are copolymerizable with said unsaturated acid component. Typically, such comono-mers do not contain free carboxylic acid groups and are esters containing ~ ethylenic unsaturation in the acid or alcohol portion: hydrocarbons, both aliphatic and aromatic, containing ~ ethylenic unsaturation, such as the C4-C12 alpha olefins, Por example isobutylene, hexene, nonene, dodecene, etc.;
styrenes, for example styrene, ~-methyl styrene, p-methyl styrene, p-sec. butyl styrene, etc.; and vinyl monomers, for example vinyl acetatel vinyl chloride, vinyl ketones such as methyl and ethyl vinyl ketone, et~. Comonomers containing ~unctional groups which may cause crosslinking, ge7ation or other interfering reactions should be avoided, although minor amounts o~ such comonomers (up to about 10% by weight of the comonomer system~ oPten can be tolerated.

Specific useful copolymerizable comonomers include the following:

(A) Esters of saturated acids and unsat-urated alcohols wherein the saturated acids may be monobasic or polybasic acids containing up to about 40 carbon atoms such as the following: acetic, propionic, butyric, valeric, caproic, stearic, oxalic, malonic, succinic, glutaric, adipic, pime-lic, suberic, azelaic, sebacic, phthalic, isophtha lic, terephthalic, hemimellitic, trimellitic, trimesic and the like, including mixtures. The unsaturated alcohols may be monohydroxy or poly-hydroxy alcohols and may contain up to about 40 carbon atoms, such as the following: allyl, methally, crotyl, l-chloroallyl, 2-chloroallyl, cinnamyl, vinyl, methyl vinyl, l-phenallyl, butenyl, propargyl, 1-cyclohexene-3-ol, oleyl, and the like, including mixtures.

(B) Esters of unsaturated monocarboxylic acids containing up to about 12 carbon atoms such as acrylic, methacrylic and crotonic acid, and an esterifying agent containing up to about 50 carbon atoms, selected from saturated alcohols and alcohol epoxides. The satuarted alcohols may preferably contain up to about 40 carbon atoms and include monohydroxy compounds such as: methanol, ethanol, propanol, butanol, 2-ethylhexanol, octanol, dode-canol, cyclohexanol, cyclopentan~l, n~opentyl alcohol, and benzyl alcohol; and alcohol ethers such as the monomethyl or monobutyl ethers o~ ethylene or propylene glycol, and the like, including mixtures.
The alcohol epoxides include fatty alcohol epoxides, glycidol, and various derivatives of alkylene oxides, epichlorohydrin, and the like, including mixtures.

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The components of the graft copolymeriz-able system are used in a ratio of unsaturated acid monomer component to comonomer component of about 1:4 to 4:1, preferably about 1:2 to 2:1 by weight.

The grafting of the ethylene copolymer with the carboxylic acid material may be by any suitable method, such as thermally by the "ene"
reaction, using copolymers containing unsaturation, such as ethylene-propylene diene polymers either chlorinated or unchlorinated, or more pre~erably it is by free-radical induced graPting in solvent, preferably in a mineral lubricating oil as solvent.

The radical grafting is prePerably carried out using free radical initiators such as peroxides, hydroperoxides, and azo compounds and preferably those which have a boiling point greater than about 100C and which decompose thermally within the grafting temperature range to provide said free radicals. Representative of these free-radical initiators are azobutyro-nitrile, 2,5-dimethyl-hex-3-yne-2, 5 bis-tertiary-butyl peroxide (sold as Lupersol 130) or its hexane analogue, di-tertiary butyl peroxide and dicumyl peroxide. The initiator is generally used at a level of between about 0.005%
and about 1%, based on the total wsight of the pol~mer solution, and temperatures of about 150 to 22~C.

The ethylenically unsaturated carboxylic acid material, prePerably maleic anhydride, will be generally used in an amount ranging from about 0.01%
to about 10%, preferably 0.1 to 2.0%, based on weight of the initial total solution. The aforesaid carboxylic acid material and free radical initiator are generally used in a weight percent ratio range of 1:1 to 30:1, preferably 3:1 to 6:1.

The amine component will have two or more primary amine groups, wherein the primary amine groups may be unreacted, or wherein one of the amine groups may already be reacted.

Particularly preferred amine compounds have the following formulas:

(A) alkylene polyamines H--N----alkylene--7 t H
H H
x wherein x is an integer of abou$ 1 to 10, preferably about 2 to 7, and the alkylene radical is a straight or branched chain alkylene radical having 2 to 7, pre~erably about 2 to 4, carbon a~oms:

(B~ polyoxyalkylene polyamines NH2 al kyl ene ~ O--al kyl ene~ NH2 ( i ) m where m has a value of about 3 to 70, preferably 10 to 35; and R ~ alkylene ~ O--alkylene t NH2)3-6 n where n has a value of about 1 to 40 with the provision that the sum of all the n's is from about f~

3 to about 70, preferably from about 6 to about 35, and R is a polyvalent saturated hydrocarbon radical of up to ten carbon atoms having a valence of 3 to 6. The alkylene groups in either formula (i) or (ii) may be straight or branched chains containing about 2 to 7, preferably about 2 to 4, carbon atoms.

Examples of the alkylene polyamines of formula (A) above include methylene amines, ethylene amines, butylene amines, propylene amines, pentylene amines, hexylene amines, heptylene amines, octylene amines, other polymethylene amines, the cyclic and higher homologs of these amines such as the pipra-zines, the amino-alkyl-substituted piperazines, etc.
These amines include, for example, ethylene diamine, diethylene triamine, triethylene tetramine, propy-lene diamine, di(heptamethylene)triamine, tripropy-lene tetramine, tetraethylene pentamine , trimethy-lene diamine, pentaethylene hexamine, di(trimethy-lene)triamine, 2-heptyl-3-(2-aminopropyl)imidazo-line, 4-methylimidazolinet 1,3-bis(2-aminoethyl)imi-dazoline, pyrimidine, 1-(2-aminopropyl)piperazina, 1,4 bis-(2-aminoethyl)piperazine, N,N-dimethyamino-propyl amine, N,N-dioctylethyl amine, N-octyl-N~-methylethylene diamine, 2-methyl-1-t3-aminobutyl)-piperazine, etc. Other higher homologs which may be used can be obtained by condensing t~o or more of the above-mentioned alkylene amines in a known manner.

The ethylene amines which are particularly useful are described, for example, in the Encyclo-pedia of Chemical Technology under the heading of "Ethylene ~mines" (Kirk and Othmer), Volume 5, pgs.
898-905; Interscience Publishers, New York (1950).

The polyoxyalkylene polyamines of formula (B) above, preferably polyoxyalkylene diamines and polyoxyalkylene triamines, may have average mole-cular weights ranging from about 200 to about 4000 and preferably from about 400 to about 2000. The preferred polyoxyalkylene polyamines include the polyoxyethylene and polyoxypropylene diamines and the polyoxypropylene triamines having average molecular weights ranging ~rom about 200 to 2000.
The polyoxyalkylene polyamines are commercially available and may be obtained, for examples, from the Jefferson Chemical Company, Inc. under the trade name "Jeffamines D-230, D-400, D-1000, D-2000, T-403!', etc.

The acid component includes: hydrocarbyl substituted succinic anhydride or acid having 12 to 49 carbons, preferably 16 to 49 carbons in said hydrocarbyl group; long chain monocarboxylic acid of the formula RCOOH where R is a hydrocarbyl gxoup o~
50 to 400 carbons and long chain hydrocarbyl substi-tuted succinic anhydride or acid having 50 to 400 carbons in said hydrocarbyl group. Said hydrocarbyl groups are essentially alphatic and includ~ alkenyl and alkyl groups. The longer chain acids and anhydrides are preferred, particularly when the grafting reaction is carried out in lubricating oil because o~ its ability to impart dispersancy to reacted oil molecules as well as their greater solubilizing effect.

.3 7, Primarily because of its ready availabil-ity and low cost, the hydrocarbyl portion (e.~.
alkenyl groups) of the carboxylic acid or anhydride is pre~erably dPrived from a polymer of a C2 to Cs monoolefin, said polymer generally having a molecu-lar weight of about 140 to 6500, e.~. 700 to about 5000, most preferably 700 to 3000 molecular weight.
Particularly preferred is polyisobutylene.

The aforesaid amine and acid component may be prereacted, with the acid being generally attached to the amine through salt, imide, amide, amidine, ester, or other likages so that a primary amine group of the polyamine is still available for reaction with the acid moieties of the gra~ted polymer.

The amount of the ethylene copolymer containing amine ~unctionality in the grease compo-sition need only be that which improves the water resistance of the grease. Typically, however, the amount of copol~ner will range from about 0.01 to about 4 wt.%, preferably from about 0.1 to about 2 wt.%, based on weight of the grease, although larger amounts could be used if desired.

The particular copolymer e~ployed in this invention can be readily obtained in the market-place. As such, its methods of preparation is well known to those skilled in the art (see U.S.
~,517,104).

The grease composition may also contain small amounts o~ supplemental additives which include, but are not limited to, anticorrosive agents, extreme pressure antiwear agents, pour point depressants, tackiness agents, oxidation inhibitors, dyes, and the like, which are incorporated for specific purposes. The total amount of these additives will typically range from about 2 to about 5 wt.% based on total weight of the grease composi-tion. In addition, solid lubricants such as moly-bdenum disulfide and graphite may be present in the composition - typically from about 1 to about 5 wt.%
~preferably from about 1.5 to about 3 wt.%) for molybdenum disulfide and rom about 3 to about 15 wt.% (preferably from about 6 to about 12 wt.%) for graphite.

The grease composition of this invention is usually prepared in situ by chemically reacting or mecahnically dispersing thickener components in the lubrica~ing oil for from about 1 to about 8 hours or more (preferably from about 3 to about 6 hours) followed by heating at elevated temperature (e.q., from about 140 to about 225C depending upon the particular thickener used) until the mixture thickens. In some cases (e.~. a simple lithium grease), a preformed thickener can be use~. The mixture is then cooled to ambient temperature (typically about 60C) during which time the ethylene copolymer and other additives are added.
The polymer and the other additives can be added together or separately in any order.

The components of the grease composition can be mixed, blended, or milled in any number of ways which can readily be selected by one skilled in J

the art. Suitable means include external mixers, roll mills, internal mixers, Banbury mixers, screw extruders, augers, colloid mills, homogenizers, and the like.

The grease composition of this invention may be suitably employed in essentially any applica-tion requiring good water resistance. Examples of such applications include steel mills, underground mining, and the like. The composition, however, is particularly well suited for use in steel mill applications.

This invention will be further undPrstood by reference to the following examples which are not intended to restrict the scope of the claims appended hereto.

Example 1 - Water Spray-Off of a Lithium Grease Without Ethylene-Propylene Copolymer A base grease was prepared in a commercial gas-fired grease kettle from the following ingre-dients:

Weiyht (kg.) per 1000 In~redientskq. of Base Grease 1200 Coastal Pale 897.4 ~ithium Hydroxide Monohydrate 12.6 Fatty Acid 90.0 The fatty acid (which contains about 96.5 wt.~12-hydroxy stearic acid) was dissolved in approxi-mately 50% of the 1200 Coastal Pale (a naphthenic oil having a viscosity of 229 cSt at 40C) followed 2 ~

by neutralization o~ the resulting product with lithium hydroxide monohydrate previously dispersed in water (in the ratio of 0.4 kg. to 1 kg. of water). The mixture was heated to approximately 110C, adjusted to an alkalinity equivalent to 0.05 to 0.15 wt% NaO~, and further heated to about 196~C.
The remainder of the oil was added, and the product cooled to ambient temperature, filtered, and homo-genized in a colloid mill to form the base grease.

A diluent oil of 105 Coastal Pale (a naphthenic oil having a viscosity of 21 cSt at 40C~
was added to the base grease and blended in a Hobart mixer until the resulting grease (Grease A) had an NLGI No. 1 consistency (310-340 dmm. penetration X60).

The water spray-off (a measure of water resistance) of Grease A was determined using ASTM D
4049 "Resistance of Lubricating Grease to Water Spray" ~the disclosure of which is incorporated herein by reference), in which a steel panel was coated with a l/32 inch layer o~ grease and then sprayed with water controlled to 38 + 0.5C and 276 kPa. At the end of about 5 minutes, the amount of grease removed was determined, and spray-off reported as a percentage of the originai a~ount applied. The results obtained for Grease A are shown in Table 1 below.

Example 2 - Water Spray-Off of a Lithium Grease Containing Ethylene-Propylene Copolymer Without Amine Functionality Two polymer-containing blends (Greases B
and C) were then prepared by adding different 2 ~

amounts of the same ethylene-propylene copolymer to the base grease prepared above. The copol~mer was obtained as a commercial viscosity index improver in solution with Solvent 100 Neutral and then further diluted with 105 Coastal Pale for ease of handling.
The base grease, polymer, and diluent oil were blended for 30 min. in a Hobart mixer to produce greases having an NLGI No. 1 consistency. The water spxay-off of Greases B and C were then determined using ASTM D 4049 and the results obtained sum-marized in Table 1 below.

Example 3 - Water Spray-Off of a Lithium Grease Containing Ethylene-Propylene Copolymer With Amine Functionality Example 2 was repeated for several blends that contained a high molecular weight analog of an ethylene-propylene copolymer containing amine func-tionality (Greases D-H).

Although molecular weight can be estab-lished by a variety of techniques known in the art, the molecular weight of copolymers used as lubricant additives can be established by reference to their "Shear Stability Index" (or "SSI"). SSI measures the relative change in polymer viscosity due to mechanical shearing in a standard engine tes~ (L-38 10 Hr. Tast), and ranges from 0% ~or a low molecular weight copolymer to 22% or more for a high molecular weigh$ copolymer.

As in Example 2, the copolymer was ob-tained as a viscosity index improver in Solvent 100 Neutral LP and further diluted with 105 Coastal Pale 2 ~

for ease of handling. The copol~mer had an ethylene content of about 44 wt.%, an SSI of 22%, and a weight average molecular weight estimated to range ~rom about 140,000 to about 150,000. Aliquots of the copolymsr solution were blended with the base grease of Example 1 using a Hobart mixer to prepare greases having an NLGI No. 1 consistency. Copolymer concentrations ranged from 0.28 to 1.65 wt~. Water spray-off o~ Greases D-H was measured as in Example 1 and the results obtained summarized in Table 1 below.
xample 4 - Water Spray-Off of a Grease Containing a Low MW Ethylene-Propylene Copolymer With Amine Functionality ~ xample 3 was repeated using a low mole-cular weight analog of an ethylene-propylene co-polymer with amine functionality (Greases I-L). The copolymer had an ethylene content of about 44 wt.%, an SSI of zero, and a weight av~rage molecular weight estimated to be about 110,000. Copolymer concentrations ranged ~rom 0.93 to 1.86 wt%. The water spray-off o~ Greases I-L were measured as in Example 1 and the results obtained summarized in Table 1 below.

Table I

Concentr~tion, Water Spray-off, ~3~ Lll CoDolymer wt% wt~ Los~s A None o 00 9g BEthy1ene-Propylene 0.28 90 CEthyl~ne-Propylene 0.~8 70 DEthylene-Propylene 0~28 79 w. Amine Functionality High Molecu1ar Wt. (SSI=22%) E" " " " 0.38 58 F" " " " 0.56 50 G" " " " 1.11 42 H" " " " 1.65 45 IEthylene-Propylene 0.93 62 w. Amlne Functionality Low Molecular Wt. (SSI=0%) J" " " " 1.17 47 K" " " " 1.40 26 L" " " " 1.86 30 (I) Each grease had an NLGI No. I consistency.

A comparison of Greases A-C in Table shows that water spray-off is reduced (and water resistance is increased) when the grease contains an ethylene-propylene copolymer.

A comparison of Greases D-L with Greases B-C shows that a further reduction in water spray-off is obtained at the same copolymer concentrations when an ethylene-propylene copolymer with amine functionality is used.

A comparison of Greases D-H with Greases I-L shows that a still greater reduction in water spray-off is obtained when a low molecular weight analog of the ethylene-propylene copolymer with amine functionality is used. This may be seen by comparing the water spray-off at the copolymer con-centration of maximum effectiveness for the high and low molecular weight analogs. By "copolymer concen-tration of maximum effectiveness" is meant the co polymer concentration beyond which there is essen-tially no further improvement in water spray~off with copolymer addition. Thus, the "copolymer con-centration of maximum effectiveness" is about 1.1 wt.% for the high molecular weight analog and about lo 4 wt.% for the low molecular weight analog.
Accordingly, the minimum spray-off achieved is about 42 wt.% for the high molecular weight analog (Greases G and H) and about 26 wt.% for the low molecular weight analog (Greases K and L), consi-dering that the repeatability of ASTM D 4049 is ~6 wt.%.

Example 5 - Water Spray-Off oP a Lithium Complex Grease Containing an Ethylene-Propylene Copolymer With Amine Functionality A lithium complex grease was prepared in a laboratory gas-fired grease kettle using the follow-ing ingredient~:
n~redients wt.%
100 cSt Naphthenic Oil (1) 30.8 113 cSt Paraffinic Oil tl) 21.1 500 cSt Paraffinic Oil (1) 31.0 Lithium Hydroxide Monohydrate~.8 12-Hydroxy Stearic Acid 5.7 Azelaic Acid 4.4 Other Additives 4.2 (1) Viscosity at 40C.

The grease was prepared by charging a gas~fired laboratory kettle with about 70% of the oil, adding the fatty acids and heating to about 82 3 C to dissolve the components. The acids were neutralized with an aqueous dispersion of the alkali, and saponification completed by heating the reaction mixture t Q a temperature of about 200C.
After cooling the contents to about 93C, other additives (antiwear, antioxidant, and anticorrosion agents) were added, and the grease milled. The finished grease had a penetration t60X) of 330 dmm.

Examples 3 and 4 were repeated using the formulated lithium complex grease prepared above and ethylene-propylene copolymers of high and low mole-cular weight tSSI = 22~ and 0~, respectively).
Water spray-off was determined as in the previous examples and the results obtained summarized in Table 2 below.

Table 2 Concentration, Water Grease (1) Copolvmer wtX Sprav-off. wt% Loss M None -- 98 N Ethylene-Propylene 0.56 34 w. Amine Functionality (SSI = 22X) 0 Ethylene-Propylene 1.40 22 w. Amine Functionality (SSI = 0%) (1) Each grease had an NLGI No. 1 consistency.

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The data in Table 2 show that Grease M
with no copolymer had little resistance to water spray-off, wherea~ Greases N and O showed signifi-cantly greater resistance.

Claims (29)

1. A grease composition which comprises (a) a lubricating oil, (b) a water insoluble thickener, and (c) an ethylene copolymer having an amine functionality.

2. The composition of Claim 1 wherein the thickener is based on aluminum, barium, calcium, lithium soaps, or their complexes.

3. The composition of Claim 2 wherein the thickener is based on a lithium soap, a calcium soap, their complexes, or mixtures thereof.

4. The composition of claim 1 wherein the copolymer comprises from about 15 to about 90 wt.%
ethylene and from about 10 to about 85 wt.% of one or more C3 to C28 alpha olefins.

5. The composition of claim 4 wherein the alpha olefin contains a C3 to C8 alpha olefin.

6. The composition of claim 4 wherein the number average molecular weight is between about 5,000 and about 500,000.

7. The composition of claim 1 wherein the ethylene copolymer comprises the reaction product of (i) an ethylene copolymer comprising from about 15 to about 90 wt.% ethylene and from about 10 to about 85 wt.% of one or more C3 to C28 alpha-olefin wherein the copolymer has a number average molecular weight ranging from about 5,000 to about 500,000 and is grafted with an ethylenically unsatu-rated carboxylic acid material containing at least one ethylenic bond and at least one carboxylic acid groups or anhydride groups;

(ii) an alkylene or oxyalkylene amine having at least two primary amine groups selected from the group consisting of alkylene polyamines having alkylene groups of about 2 to 7 carbon atoms and 2 to 11 nitrogens, and polyoxyalxylene polyamines, wherein the alkylene groups contain 2 to 7 carbon atoms and the number of oxyalkylene groups will be about 3 to 70; and, (iii) a long chain hydrocarbyl substituted succinic anhydride or acid having 50 to 400 carbon atoms.

8. The composition of claim 7 wherein the reaction product is formed by simultaneously react-ing (i), (ii), and (iii) with removal of water.

9. The composition of claim 8 wherein (ii) and (iii) are first pre-reacted followed by reaction with (i). 1

10. The composition of claim 8 wherein (i) comprises a copolymer containing from about 30 to about 80 wt.% ethylene and from about 20 to about 70 wt.% propylene, having a number average molecular weight in the range of about 10,000 to 200,000 grafted with maleic anhydride.

11. The composition of claim 10 wherein (i) comprised ethylene and propylene grafted with maleic anhydride, wherein about 1 to 2 molar propor-tions of (ii) and about 1 to 4 molar proportions of (iii) are used per molar proportion of maleic anhydride moiety.

12. The composition of claim 8 wherein (iii) is a hydrocarbyl substituted succinic acid or anhydride in which the hydrocarbyl substituent is an alkenyl or alkyl group derived from a polymer of C2 to C5 mono-olefin.

13. The composition of claim 12 wherein the carboxylic acid is polyisobutenyl succinic anhydride having about 50 to 400 carbon atoms in the polyisobutenyl group.

14. The composition of claim 8 wherein the amine is alkylene polyamine of the general formula wherein x is about 1 to 10 and the alkylene radical is ethylene.

15. The composition of claim 8 which comprises the reaction product of 5 to 30 wt.% of the ethylene copolymer in 95 to 70 wt.% of a mineral lubricating oil, free radical grafted with maleic anhydride whereby both the copolymer and some oil have become reacted with maleic anhydride, then reacting with a mixture of diethylene triamine and polyisobutenyl succinic anhydride having 50 to 400 carbons in said polyisobutenyl substituent.

16. The composition of claim 8 which is the reaction product of 5 to 30 wt.% of ethylene-propylene copolymer in 95 to 70 wt.% mineral lubri-cating oil free radical grafted with maleic anhy-dride using a free radical peroxide initiator, and further reacted with an ashless dispersant reaction product of about 1 to 2 moles polyisobutenyl suc-cinic anhydride having 50 to 400 carbons in said polyisobutenyl substituent with a molar proportion of diethylene triamine.

17. The composition of claim 16 which is finally treated with an alkyl benzene sulfonic acid having an average of about 24 carbons in said alkyl group.

18. The composition of claim 8 wherein 5 to 30 wt.% of ethylene-propylene copolymer in 95 to 70 wt.% mineral lubricating oil is free radical grafted with maleic anhydride using a peroxide initiator, and is then simultaneously reacted with diethylene triamine and polyisobutenyl succinic anhydride.

19. A grease composition comprising (a) from above about 50 to about 90 wt.%
of a lubricating oil, (b) from about 1 to about 15 wt.% of a thickener based on a lithium soap, a calcium soap, their complexes, or mixtures thereof, and (c) from about 0.01 to about 4 wt.% of an ethylene-propylene copolymer having an amine functionality, an ethylene content between about 15 to about 90 wt.%, and a number average molecular weight between about 5,000 and about 500,000.

20. The composition of Claim 19 wherein the thickener is a lithium soap or a lithium complex soap based on an hydroxy fatty acid having from 12 to 24 carbon atoms.

21. The composition of Claim 20 wherein the hydroxy fatty acid comprises an hydroxy stearic acid.

22. The composition of Claim 21 wherein the hydroxy stearic acid comprises 12-hydroxy stearic acid.

23. The composition of claim 19 wherein the ethylene content is between about 30 to about 80 wt.%.

24. The composition of claim 23 wherein the number average molecular weight is between about 10,000 and about 300,000.

25. The composition of claim 24 wherein the number average molecular weight is between about 20,000 and about 175,000.

26. A method for increasing the water resistance of a grease composition containing (a) from above about 50 to about 90 wt.%
of a lubricating oil, and (b) from about 1 to about 15 wt.% of a water insoluble thickener, which method comprises adding to said composition from about 0.01 to about 4 wt.% of an ethylene-propylene copolymer having an amine functionality, an ethylene content of from about 15 to about 90 wt.%, and a number average molecular weight ranging between about 5,000 and about 500,000.

27. The method of Claim 26 wherein the thickener is based on a lithium soap, a calcium soap, their complexes, or mixtures thereof.

28. The method of Claim 27 wherein the thickener is a lithium soap or a lithium complex soap based on an hydroxy fatty acid.

29. The method of Claim 28 wherein a pure hydrocarbon solvent, a mixed hydrocarbon solvent, a chlorohydrocarbon solvent, or mixtures thereof is added to the lubricating composition.