US3856687A - Acid neutralizing accelerating compositions - Google Patents

Abstract

Acid neutralization accelerating compositions are disclosed comprising: (a) lubricating oil base, (b) an imidazoline polyalkoxylated compound, (c) a sulfonate or phenate dispersant, and (d) an alkaline earth metal carbonate.

Description

United States Patent 1191 1111 3,856,687 Lowe Dec. 24, 1974 ACID NEUTRALIZING ACCELERATING [56] References Cited COMPOSITIONS UNITED STATES PATENTS Inventor: Warren Lowe, El C Ca 2,833,717 5/1958 Whitacre 1. 252/334 2,964,473 12/1960 Hughes et al. 1 1 252/334 [73] Asslgnee' Research Company 3,368,971 2/]968 Retzloffet al. 252/334 Francisco, Calif.

[ Filedi N V- 5, 1973 Primary Examiner-Daniel E. Wyman 21 A l. N 413,144 Assistant Examiner-l. Vaughn 1 pp D Attorney, Agent, or FirmG. F. Magdeburger; C. J.

Related U-S. Application Data Tonkin; Nelson [63] Continuation of Ser. No. 142,838, May 10, 1971, abandoned, which is a continuation-in-part of Ser. No. 45,567, June 11, 1970, Pat. No. 3,711,406. [57] ABSTRACT Acid neutralization accelerating compositions are dis- [52] US. Cl 252/33.4, 252/33, 252/427, closed comprising: (a) lubricating oil base, (b) an im- 252/51.5 R, 252/389 R idazoline polyalkoxylated compound, (c) a sulfonate [51] Int. Cl. ClOm 1/40, ClOm 1/32 or phenate dispersant, and (d) an alkaline earth metal [58] Field of Search 252/334, 33, 389 R, 42.7, carbonate.

3 Claims, N0 Drawings ACID NEUTRALIZING ACCELERATING v COMPOSITIONS CROSS-REFERENCES This application is a continuation of application Ser. No. 142,838 filed May 10, 1971, now abandoned, which in turn is a continuation-in-part of U.S. application Ser. No. 45,567, filed June 11, 1970, now U.S. Pat. No. 3,711,406.

BACKGROUND OF THE INVENTION 1. Field of the Invention Lubricating oils are employed not only for lubrication, but as a vehicle to promote the protection of the surfaces lubricated by the oil. The tendency for rusting has required that lubricating oils include additives which inhibit rust. Also included in lubricating oils for internal combustion engines are bases capable of neutralizing the acids formed during fuel combustion or introduced into the oil by blow-by or other mechanisms.

The oxidation of hydrocarbon oils yields a variety of compounds that are deleterious for the service for which the oils are intended. A large variety of end products result from the oxidation. Among those identified are lactones, ketones, aldehydes, esters, alcohols, hydroxy acids, anhydrides, peroxides, and acids. The acidic and peroxidic components attack metals, corrode bearings, and promote wear and rust. Acidic products are also a major source of the oil insolubles that cause ring sticking, sludging, and impede oil flow.

Diesel fuels contain varying amounts of sulfur which is oxidized in combustion and mainly exhausted from the engine. However, appreciable quantities are blown through the ring zone together with air and water. Under these conditions, the S is converted to S0 which in turn is converted to sulfuric acid. This results in acidic attack on the oil, rings and cylinders.

While gasoline fuels are low enough in sulfur content so that sulfuric acid attack should pose no problem, the blow-by of fuel oxidation products and water which accumulate in the crankcase lead to sludging, corrosion and lacquer formation.

The three important mechanisms available for inhibiting rust and corrosion are acid neutralization, inhibition of oil oxidation and protective film formation. Since acids are involved in the rust and corrosion processes, it is obvious that their neutralization will serve as a preventative. This is a function performed by alkaline earth metal carbonates, which when dispersed in a lubricating oil by means of a metal salt dispersant (phenate or sulfonate) will maintain low copper-lead bearing corrosion rates and inhibit rusting as long as the pH of the oil is above 6. Furthermore, it has been shown that in the diesel engine corrosion by sulfuric acid is prevented as long as the pH of the oil is maintained above 4.5. Ring and cylinder wear in gasoline engines operating under low temperature conditions (jacket temperature 32C.) increases sharply when the pH of the oil drops below 6 [W. T. Stewart and F. A. Stuart, Advances in Petroleum Chemistry and Refining, Vol. 7, p. l (1963)].

Rusting and acidic corrosion also constitute a serious problem in steam turbines and other machinery exposed to moisture. Like the internal combustion engine corrosion discussed previously, this type of corrosive wear is readily controlled by effective alkaline additives.

2. Description of the Prior-Art In U.S. Pat. No. 3,458,444, alkenyl succininates of hydrocarbon-substituted ethanolamines are taught as rust inhibitors. Various alkanolamines are taught in U.S. Pat. Nos. 3,197,510 and 3,398,197, the compounds having a widevariety of uses. Esters of the imidazolines are taught as corrosion inhibitors in U.S. Pat. No. 3,017,352.

U.S. Pat. Nos. 2,681,315 and 2,833,717 teach lubricating oil compositions containing poly(oxyethylene)alkylphenol useful as rust or corrosioninhibiting additives. US. Pat. No. 2,921,027 teaches poly(oxyethylene)sorbitan fatty acid ester as a rust inhibitor. U.S. Pat. Nos. 2,620,302, 2,620,304, and 2,620,305 teach 1,2-poly(oxyalkylene)glycol lubricating compositions. Alkaline earth metal salt dispersants are also mentioned in some of the foregoing patents. U.S. Pat. No. 3,509,052 teaches the use of succinic acid derivatives in combination with poly)oxyalkylene)polyols and U.S. Pat. No. 3,567,784 is also concerned with the poly(oxyalkylene)polyols.

SUMMARY The compositions of this invention are a combination of a polyalkoxylated compound and an alkaline earth metal carbonate dispersed in an oil of lubricating viscosity. The presence of a polyalkoxylated compound in the composition promotes the neutralization of acid from an aqueous phase mixed with the oil as determined by pH measurements. The compositions provide rust and corrosion protection.

DESCRIPTION OF THE INVENTION The combination of certain polyalkoxylated compounds and alkaline earth metal carbonates dispersed in an oil of lubricating viscosity in accordance with the present invention results in surprising improvement in the rate of acid neutralization as demonstrated by the acid neutralization rate test to be described further. The use of certain polyalkoxylated compounds in combination with the dispersed carbonate inhibits rust formation and corrosion of ferrous metal surfaces coming into contact with lubricants containing said combinations. The polyalkoxylated compounds are present in amounts from 0.01 to about 5.0 percent by weight of the composition. These compounds are certain oilsoluble alkyl or alkenyl amines, glycols, alcohols, imidazolines, acids and phenols which are polyalkoxylated as described below.

The alkaline earth metal carbonate will normally be present to provide alkalinity values of from about 0.5 to mg. KOH/g, more usually from about 1 to 20 mg. KOH/g. (for method of determination, see Abbott & Farley, Methods and Significance of Base Determination in Marine Cylinder Lubrication Oils, 23rd ASLE Meeting, May, 1968.) While alkalinity values in excess of 10 mg. KOH/g. are not essential to rusting protection, values in excess of 10 mg. KOH/g. will frequently be used for a particular service. In marine lubrication, alkalinity values are high, while in automobile lubrication, alkalinity values are relatively low.

Other additives may also be included to fulfill functions other than those provided for by the dispersed carbonate base and polyalkoxylated compound, as well as to augment the functions of the latter additives.

The other additives will be present in varying amounts, the total amount of other additives normally not exceeding 15 weight percent and usually not being less than 0.1 weight percent. These additives include ashless dispersants such as succinimides, hydrocarbyl alkylene polyamines, etc., dithiophosphates, carboxylic acid corrosion inhibitors, etc.

Components Polyalkoxylated Compounds These compounds are of the general formula Y (R O),,H wherein R is a C -C alkylene radical and a is in the range from I to about 12. Among other possible embodiments of the invention, to be discussed subsequently, Y can be the phenoxy fragment having the forwherein R is an aliphatic hydrocarbyl radical of molecular weight in the range from about 50 to about 2000. If R is an alkyl group, and R is CI-I CH then the compound is an alkyl phenoxy poly- (oxyethylene)ethanol.

R is an alkylene radical of 2-5 carbon atoms representing the hydrocarbyl portion of the one or more alkylene oxide units incorporated into the molecule. For example, preferably R is the propylene oxide unit CH(CI-I )CH O, or most preferably, the ethylene oxide unit CH CI-I O.

R is an alkyl or alkenyl radical of about 5 or more carbon atoms, and has a molecular weight in the range from about 50 to 2000. The alkyl or alkenyl groups can be straight-chain or branched or partially straight-chain and partially branched. Preferably R is an alkyl or alkenyl having 0 to 2 sites of unsaturation. The R group can be derived from synthetic or natural sources. Illustrative R groups are dodecyl, tetradecyl, hexadecyl, octadecyl, etc. Dodecadienyl, n-octadecadienyl, hexadecenyl, etc. R can be polyisobutenyl or other polymers of olefin monomers of from 2 to 6 carbon atoms, and preferably from 3 to 4 carbon atoms.

Illustrative examples of the polyalkoxylated phenoxy compounds within the scope of the present invention are nonylphenoxy poly(oxyethylene)ethanol, dodecyl phenoxy poly(oxyethylene)-ethanol, dodecyl phenoxy poly(oxypropylene)propanol, hexadecadienyl phenoxy poly(oxyethylene)ethanol, etc.

In another embodiment of this invention, Y is the fatty acid fragment R COO and Y(R O),,H is a polyoxyalkylene fatty acid ester. In still another embodiment, Y is the alcoholic fragment, R CH O and Y(R-. 0),,H is an alkyl or alkenyl poly(oxyalkylene)alkanol.

Illustrative alkyl poly(oxyalkylene)alkanols and alkenyl poly(oxyalkylene)alkanols which fall within the scope of the present invention include decyl poly(oxyethylene) ethanol, dodecyl poly(oxypropylene)- propanol, octadecenyl poly(oxyethylene)ethanol, etc., all of the general formula, R CI-I O(RO),,I-I. Of these, the alkyl poly(oxyethylene)ethanols are the preferred embodiment.

Illustrative poly(oxyalkylene) fatty acid esters which are included within the scope of this invention are of the general formula R COO(R O),,H and include poly(oxyethylene)stearate, poly-(oxyethylene)laurate, poly(oxyethylene)oleate, poly(oxypropylene)-stearate, etc.

The conversion of an aliphatic alcohol, alkyl phenol or fatty acid into a polyoxyethylene derivative can be accomplished according to base catalyzed reactions which are well known in the literature.

The effectiveness of ethoxylation catalysts increases with their basicity. Ratios of0.005-0.5 mole of NaOH, NaOCH or KOH per mole of reactant are frequently used. Reaction temperatures range from l00-200C. depending upon the reactant and the properties desired, i.e., degree of ethoxylation. In general, the polyoxyalkylene surfactants are polydispersed mixtures of compounds that differ in the polymer chain length. However, their properties approximate those of the molecule represented by their average composition.

In yet another embodiment of this invention, Y is HO(R O) (CH(CH )CH O), and Y (RO),,H is a poly(oxypropylene)-poly(oxyethylene) glycol. R is ethylene, d is in the range from 0 to about and e is l to about l2. Propylene oxide is reacted with propylene glycol (l,2-propane diol) to form a series of polyoxypropylene hydrophobes with molecular weights of 800 and greater. The molecular weight of the polyoxypropylene glycol must be at least 800 for it to function as a hydrophobe. These hydrophobes are then made amphipathic by ethoxylation to polyoxyethylene contents of 2090 percent of the total weight. A series of products of this composition is marketed by Wyandotte Chemicals Corporation under their Pluronic trademark. Nitrogen Containing Polyalkoxylated Compounds In still another embodiment of this invention, Y is an alkylor alkenyl-substituted imidazoline nucleus and Y(RO),,H is an alkyl or alkenyl imidazopoly(oxyalkylene)alkanol. In a preferred embodiment the oxyalkylene is oxyethylene. For illustrative purposes, compounds within the scope of this embodiment include oleyl imidazo poly(oxyethylene)ethanol, heptadecyl imidazo poly(oxyethylene)ethanol, heptadecenyl imidazo poly(oxyethylene)ethanol, etc.

In a further embodiment of this invention, Y is itself a polyalkoxylated fragment of the formula wherein R is a C -C alkylene, R and R are as heretofore described, a is from I to about 12, as heretofore defined, b and b' in the range from O to about 12 and c is 0 or I. Preferably R is an alkylene of 2-3 carbon atoms. Illustrative compounds which find use within the scope of this invention are N,N,N'-tri(2-hydroxy ethyl)N-octadecyl propylene diamine, N,N,N'-tri(3- hydroxypropyl)-N-octadecadienyl propylene diamine, N,N-di(2-hydroxy ethyl)stearyl amine, N,N-di(3- hydroxy propyl)tetradecylamine, etc. R may be a polymer of an olefin monomer of from 2 to 6 carbon atoms. In a preferred embodiment of this invention R is a polybutenyl radical having a number average molecular weight of about 1400. The polybutene polyamine is, for example, the product of the reaction of a chlorinated polyisobutylene and ethylene diamine.

Some polyalkoxylated compounds suitable for use in this invention are commercially available under various trade names. Thus, suitable compounds include certain block copolymers of propylene oxide and ethylene oxide, such as the Pluronics (Wyandotte Chemicals); the poly(oxyethylene) alcohols such as the Neodols (Shell); poly(oxyethylene)amines, such as Ethoduomeens (Armour); poly(oxyethylene)imidazolines, such as Monazolines (Mona Industries); poly(oxyethylene)acids, such as Nonisols (Geigy) and Ethofats (Armour).

The over-all structure of these molecules is amphipathic and purposely so. An amphipathic molecule is an organic species encompassing in the same molecule two dissimilar structural groups, e.g., a water soluble and a water insoluble moiety. The composition, solubility properties, location, relation and relative sizes of these dissimilar moieties in relation to the over-all molecular configuration determines the efficacy of the polyalkoxylated compound for our purposes.

A variety of names have been used to describe the opposing properties of the moieties which make up an amphipathic molecule, e.g., hydrophobic-hydrophilic, lipophilic-lipophobic, oleophilic-oleophobic, and simply polar-nonpolar. In compounds of the class used in this invention, the polyoxyalkylene chain, (R O),,, is the water solubilizing (hydrophilic, polar or lipophobic) moiety and Y, mainly the hydrocarbyl R is the oil solubilizing (hydrophobic, nonpolar, or lipophilic) moiety.

The molecular weights of the amphipathic molecules found to be useful in the present invention range from a low of about 150 up to an average molecular weight of about 4500 when Y is a polymeric substance. For the purposes of the present invention, for each polyalkoxylated compound, there is an optimum solubility'and polar balance between the hydrophilic and hydrophobic moieties. Relatively small changes in the composition of the amphipathic molecule are sufficient to change its relative solubility and synergistic acid neutralization effect in conjunction with dispersed alkaline earth metal carbonates.

Thus the value of a which specifies the degree of polyalkoxylation can vary from 1 to about 12, but could exceed this greatly. The value of a must be balanced against the carbon number, chain length and degree of unsaturation in the hydrocarbyl radical R as well as the nature of the remainder of the Y fragment, whether phenoxy, alkoxy, heterocyclic, etc.

Alkaline Earth Metal Carbonates The alkaline earth metal carbonates are magnesium, calcium and barium carbonates, preferably calcium and barium carbonates. Small amounts of the hydroxides of the metals may also be present, usually not contributing more than about percent of the alkalinity value from the alkaline earth metal carbonate composition. The alkaline earth metal compounds are not soluble in hydrocarbon media. Therefore, they are invariably dispersed with some type of metal salt dispersant.

These dispersants are well known in the art and will be discussed only summarily.

The preferred dispersants are the sulfonate and phenate dispersants. The sulfonates are extensively discussed in US. Pat. No. 3,488,284. The organic sulfonates are prepared either from natural or synthetic sources. The natural sulfonates are referred to as mahogany sulfonates and are derived from petroleum mineral oil fractions and normally have from about 25 to 50 carbon atoms per sulfonic acid. Synthetic sources are also employed which are usually alkylated benzenes having from about 25 to 50 carbon atoms. The use of the sulfonates and the method of preparing overbased sulfonates is well known, as already indicated by the above patent. Other patents include US. Pat. Nos. 3,021,280, 3,256,186, 3,057,896 and 3,312,618.

Another class of dispersant for alkaline earth metal carbonates are the phenates. The phenates are alkylated phenols either individually or polymerized to a low order of from 2 to 5 alkyl phenols, normally bridged with sulfur, alkylene groups, or di(alkylene) amino groups (Mannich bases). The alkyl group on the phenol is normally of at least 8 carbon atoms and usually does not exceed 36 carbon atoms, more usually being in the range of about 12 to 30 carbon atoms. The phenoxide in the phenate also contributes to alkalinity value.

The overbased phenates are described in numerous patents such as US. Pat. Nos. 3,474,035, 3,429,812 3,388,063, 3,336,224 and 2,798,852.

Other dispersants which are also employed are the alkaline earth metal alkyl phosphonates and thiophosphonates. The phosphonates will normally be at least about 30 carbon atoms and may be as high as 200 carbon atoms, more usually from about 50 to carbon atoms. These overbased phosphonates are described in US. Pat. No. 3,312,618.

Another group of dispersants are the succinimides of alkylene polyamines. These dispersants usually have an alkyl or alkenyl group bonded to the succinimide group of at least 50 carbon atoms and not more than about 200 carbon atoms. The alkylene polyamines are normally ethylene or propylene polyamines having from 2 to 6 amino groups, more usually from 3 to 5 amino groups. Carboxylates also find use as dispersants. See US. Pat. No. 2,865,951.

The alkalinity value of the overbased dispersants will usually be at least and not exceed 500, more usually being in the range of about 200 to 450 mg. KOH/g. The equivalent ratio of base to dispersant will be at least 1 to 1 and more usually at least 1.5 to 1, normally not exceeding about 20 to 1.

These compositions are used in a sufficient amount to provide the desired alkalinity value in the final composition. Therefore, the alkaline earth metal carbonates are prepared as concentrates and then diluted in the lubricating oil medium with the polyalkoxylated compound to provide the desired end composition. Lubricating Oils The oils which find use in this invention are oils of lubricating viscosity derived from petroleum or synthetic sources. The oils may be paraffinic, ester, naphthenic, halo-substituted hydrocarbons, asphaltic or combinations thereof. Oils of lubricating viscosity normally have viscosities in the range of 35 to 50,000 Saybolt Universal Seconds (SUS) at 100F., more usually from about 50 to 10,000 SUS at 100F.

Other Additives Other additives are desirably included in the composition. These additives may be pour point depressants, oiliness agents, antioxidants, detergents (particularly succinimides), corrosion inhibitors, extreme pressure agents, etc. Usually, for oils to be used in an engine, the total amount of these additivies will range from about 0.1 to 15 weight percent, more usually from about 0.5 to 10 weight percent. The individual additives may vary in amount from about 0.01 to 10 weight percent of the total composition. In concentrates, the weight percent of these additives will usually range from about 0.3 to 30 weight percent.

A preferred aspect of using the compositions of this invention in lubricating oils is to include in the oil from about I to 50 mM./kg. of a dihydrocarbyl phosphorodithioate, wherein the hydrocarbyl groups are from about 4 to 36 carbon atoms. Usually, the hydrocarbyl groups will be alkyl or alkaryl groups. The remaining valence of the phosphorodithioate will usually be satisfied by zinc, but polyalkyleneoxy or a third hydrocarbyl group may also be used. (Hydrocarbyl is an organic radical composed solely of carbon and hydrogen which may be aliphatic, alicyclic or aromatic. In this invention, the preferred hydrocarbyl groups are free of aliphatic unsaturation.)

Neutralization Rate Test The Neutralization Rate Test (NRT) consists of the neutralization of an acidic aqueous phase with a basic oil phase. The progress of the neutralization is followed with a pH meter by measuring the pH at l5-second, 30- second, or some other convenient interval. The pH is then plotted versus the time. Lubricating oil compositions containing dispersed alkaline earth metal carbonate will neutralize the acid and exhibit a definite point of inflection (PI) usually in the pH range of 3.5 to 6.5, but the time elapsed to the point of inflection (TPI) varies very widely, depending on the presence or absence of a neutralization promoter of the present invention, all other test factors being kept constant.

It is believed that the PI corresponds to the first end point for the acid-base titration in the given system. For example, the first end point in the purely aqueous titra- Composition tion of 0.01 N HCl with 0.02 N sodium carbonate occurs at pH 4.5 and is believed to correspond to the con version of HCl to carbonic acid. A second end point occurs at pH 8.1 believed corresponding to the conversion of dissolved carbonic acid to bicarbonate.

The time elapsed from initial mixing of oil and aqueous phases to the PI is the TPI, and it forms the basis for comparing various oil compositions. In general, in the comparison of two oil compositions the one with a low TPI rating (fast acid neutralization) has appeared to have better rust performance than the composition with high TPI (slow acid neutralization) all other factors being kept constant. In examples to be elaborated below, the performance of the lubricating oil compositions in the well-known Sequence IIB Engine Test were shown to be related to NRT results in these cases, all other factors being kept constant.

Thus the NRT is used to test the efficacy of the polyalkoxylated material as an oil soluble promoter of neutralization. The test procedure is as follows. A 250ml. beaker containing aqueous HCl (0.0] to 0.003 N) is fitted into a test stand with a stirring paddle and the electrodes of a Beckman Expandomatic pH meter immersed in the solution. The stirrer is a Waco power stirrer operated at about 500 rpm. The electrodes are a Calomel electrode and a Glass electrode. Since the oil phase may have a tendency to foul the Glass electrode, periodic application of Desicote (Beckman hydrophobic surface coating) should be applied as a preventive. Care should also be taken to place the electrodes and stirrer in the same relative position in the beaker for each test, and the rate of stirring should be constant for highest reproducibility.

Next the test oil composition, ml., is layered onto the aqueous phase with as little mixing as possible. The pH meter is switched on, and the stop watch and the stirrer are started simultaneously. pH readings are then made at known elapsed times and plotted versus time. The TPI will vary from more than minutes for cer tain tested oil compositions containing carbonate but having no acid neutralization promoters, to less than one minute with certain polyoxyalkylene neutralization promoters present (see Table I).

1. Reference Oil 2 C 2 C5Hi.O-(CH CH O) H 9. Poly(oxyethylene)polybutene ethylene diamine in Reference Oil TABLE I Neutralization Rate Test Weight Percent TPI H I (CH CH OH'I TABLE l-Continued Neutralization Rate Test Composition Weight Percent TPI pll ll R C N CH2 CH2 OH 1 II N l2 HO- CH2 CH2 O) CH( CH 3 CllzO CH ZCHZO ll 0 5 l 5 d 16 b+d/a 0.15

Weight: percent of acid neutralization promoter added to reference oil.

Time elapsed from start of mixing to point of inflection, in minutes pH at point of inflection. Aqueous phase 0 .01 N HCl.

Reference Oil:

zinc dialkyl dithiophosphate and 80 millimoles/kg.

a 125 neutral paraffinic oil containing 3 8 percent by weight of polyisobutenyl succinimic'e of tetraethylenepentamine 6 25 millimoles/kg. of zinc dialkylphenyl dithiophosphate 9 25 mi1limoles/k;.

of carbonated of sulfurized calcium alkyl phenate having an alkalinity value of 259 mg. KOll/g. 9 25 weight percent calcium and mole ratio of CaCO; to phenoxide of about 1. 5-2 :1.

lmportant test parameters are, first, base oil viscosity. in any comparison of lubricating oil compositions, the V of the test oils should not vary by not more than percent. Secondly, the normality of the acid. If the normality of the acid is reduced by one-half, then the TH is reduced (roughly) by one-half. This parameter may be used to adjust the scale of neutralization times in different series of tests.

Reproducibility of the NRT has been established by extensive testing, e.g., 22 tests on the same reference composition, conducted in the same way, over a period of seven months gave an average TPI of 18.6 minutes with a standard deviation of one minute.

Table I illustrates the activity of the polyalkoxylated amphipathic compounds of this invention. Composition 1 consists of the reference oil used in the test. The alkalinity value from the calcium carbonate dispersed by calcium propylene phenate is 8.9 mg. KOH/g. It also contains other additives, but it does not contain an acid neutralization promoter. As a result, the TPI for the reference oil is 167 minutes. Composition 3 shows little improvement, if any, in the TPI by the inclusion of 0.5 weight percent of a primary linear C1245 alcohol, but compositions 4 and 5 show the appreciable improvement resulting from the inclusion of polyethoxylated versions of the same alcohol.

The other results of Table I are typical of satisfactory performing additives in the NRT. In general, one looks for addition agents which substantially reduce the TPI relative to that of the reference oil (0 weight percent of acid neutralization promoter). A reduction in the TPI of better than 50 percent is regarded as evidence that the addition agent will function to help fulfill the objects of this invention. There are, of course, other properties which are needed such as additive compatibility, stability, etc. So far as rust inhibition is concerned, there is strong evidence that while a satisfactory NRT result is not quantitatively predictive of an MS Sequence llB rust rating, at the very least, the NRT result does tend to be related to the comparative rust inhibition properties of any two additives, all other fac tors being kept constant. Table II presents evidence obtained from NRT and MS Sequence IIB tests relating the average engine rust" to the pH after four minutes of mixing of an oil composition with an acidic aqueous phase. These particular results indicate that the more rapidly the pH of the mixture tends toward neutrality (a pH of 7.0 at 24C. indicates acid-base neutrality), the lower is the average engine rust formation in Sequence llB test (higher rating). The llB test is part of GM specifications and requires a 8.9 to pass.

TABLE II M S Sequence llB Lubricating Oil Average Engine Composition Rust Rating pH GM specifications require average engine rust rating of 8.9 to pass MS Sequence "8 test.

A\'erage pH after four minutes elapsed time in NRT. Into 50 ml. of 0.0l N HCI in a l50-ml. beaker with stirring bar. magnetic stirrer and Glass electrode assembly, is pipetled 25 ml. of the oil composition with minimum mixing. The stirrer and stopwatch are started simultaneously and pH readings are taken.

Further Testing A number of lubricating oil compositions were prepared by combining the appropriate amount of alkaline earth metal carbonates, specifically calcium carbonate, dispersed by either a sulfonate or a phenate with an ethoxylated amine, N-octadecyl (derived from tallow fatty acids) N,N,N'-tri(2-hydroxyethyl) propylene diamine. (Supplied by Armour & Co. as Ethoduomeen T-l3; the composition also contains about 30 percent by weight of the total composition of N-octadecyl [derived from tallow fatty acid] N,N'-di(2-hydroxyethyl) amine.) These compositions were tested in a variety of ways to establish the effectiveness of polyalkoxylated amphipathics as rust and corrosion inhibitors.

The first test is carried out as follows: A GM Oldsmo bile oil relief valve (cut lengthwise into halves) is polished with No. 2/0 emery polishing paper, rinsed with CF. hexane and then stored in hexane. The relief valve is then placed in ml. of test oil heated in a beaker at l25l30F. for one minute. An acidic solution is provided by combining 9 ml. of a solution prepared from 4 ml. of concentrated hydrochloric acid, 4 ml. of glacial acetic acid, 4 ml. concentrated sulfuric acid and 84 ml. distilled water with 300 ml. of test oil in a 400 ml. beaker. After stirring at 2000 rpm for 8 minutes, the acid solution and test oil composition are placed in an oil bath maintained at F. The treated relief valve is then put into the oil mixture with the flat surface sitting on the bottom of the beaker. After stirring at 550 rpm for 20 hours, the beaker is removed from the oil bath, the valve removed from the oil and rinsed twice with C.P. hexane and rated. The valve is rated from to 10, 0 equaling heavy rust and 10 being clean.

The test oil employed, simulating a commercially compounded oil, was an SAE 30 oil (26.7 wt. percent 130 neutral oil, 42.8 wt. percent 480 neutral oil and 30.5 wt. percent 185 bright stock; this was the base oil in all the tests unless otherwise indicated) containing 2 weight percent of a polyisobutenyl succinimide of tetraethylene pentamine (the polyisobutenyl group having a number average molecular weight of about 1000), 12 mM./kg. of zinc dialkyl dithiophosphate (alkyl of from 4 to carbon atoms) and 40 mM./kg. based on Ca of calcium carbonate dispersed with calcium mahogany sulfonate wherein the base ratio is 9.3, and the calcium carbonate composition contains 1 1.4 percent calcium. The final composition has an alkalinity value from the calcium carbonate of about 1.45.

The rust rating for the reference oil without the polyethoxylated diamine was 6.5. With 0.3 weight percent of the polyethoxylated diamine and 0.15 weight percent of the monoamine, the rust rating was 9.1 and 9.4.

The next tests which were employed are called the Humidity Cabinet Test and the Hydrobromic Acid Panel Rust Test. The Humidity Cabinet Test is ASTM D-1748 and employs a sand-blasted steel panel 1/8 inch X 2 inches X 4 inches dipped in the oil to be tested, drained of free oil at room temperature and placed in the humidity cabinet at 120F. and 100 humidity for the time specified for the results. The HBr test employs 3 sand-blasted steel panels of the same size as above immersed for no more than 1 second in 0.1 percent aqueous hydrobromic acid. Within one second of removing the test panels from the hydrobromic acid solution, the test panels are dipped in the oil to be evalu ated at room temperature. The test panels are clipped and removed from the test oil 12 times during a period of 60 seconds, after which they are suspended in air for 4 hours at room temperature and then examined for rusting. The results are compared with a commercially available rust inhibitor. tetrapropenyl succinic acid.

TABLE lIlA requires a rating of 8.9 per pass. The first test was carried out using the same reference oil as employed in Half Relief Valve Rust Test and the same ethoxylated amine composition as employed in that test. The average rust rating for the reference formulation was 8.4 and 8.8. The reference formulation with the amine had an average rust rating of 9.2.

The MS Sequence IlB Engine Test was repeated using a mid-continent W base oil containing 1.9

10 weight percent of the same succinimide employed previously, 6.25 mM./kg. of zinc dialkylphenyl dithiophosphate (alkyl is polypropenyl of from 12 to 15 carbon atoms), 9.25 mM./kg of zinc dialkyl dithiophosphate (alkyl is from 4 to 5 carbon atoms) plus the additional 15 additives set forth in the following table:

Sulfonatc Calcium mahogany sulfonate and calcium carbonate having 119.3 base ratio. 11.4 wt. 71 Ca.

N-octadccyl (derived from tallow fatty acid) N.N'.N'-tritl'hydroxyethyl) propylene diamine. Additionally. there is .15 wt. "/1 of N-nctadeeyl (derived from tallow fatty acid) diethanolamine.

Calcium carbonate dispersed calcium polypropylene phenatc (polypropylene at from 12 to 15 carbon atoms) 9.25 wt. 71 Ca. mol ratio of CaCO; to phenoxide is about 15211.

The alkalinity value derived from the m'erhased sulfonate is 1.45 mg. KOH/g.

40 The alkalinity value derived from the overhead sulfonate is 2.9 mg. KOH/g.

The alkalinity value from the overbascd phenate is 4.45 mg. KOH/g. "The alkalinity value from the overbased phenatc is 8.9 mg. KOH/g.

(Humidity Cabinet Test) (HBr Panel Rust Test) Rust lnhibitor Rust Rating (hrs) Wt. 71 l 2 3 4 (heavy rust) Ethoxylated Amine 0.45 dup- 0 0 Two specks lieate (light) runs 0 O 0 0 Reference Oil In the base oil was included 2 wt. 2 polyisobutenyl succinimide of tetraethylene pentamine (polyisobutenyl of -l000 number average molecular weight); 12 mMJkg. of zinc dialkyl dithiophosphate (alkyl offrom 4 to 5 carbon atoms; 40 mMJkg. based on Ca of calcium mahogany sulfonate overbased with calcium carbonate (9.3 base ratio. 11.4

wt. k Ca); and 0.02 wt. 1' terephthalic acid.

0.35 wt. 1 of N.N',N'-tri(Z-hydroxyethyl) N-octadecyl propylene diamine and 0.15 wt. k of N-octadccyl diethanolamine.

The next series of tests is the MS Sequence llB Engine Test. This test is part of the GM specifications and The above results demonstrate that the combination of alkaline earth metal carbonate and the poly(oxyalkylene) alkyl amines provide excellent rust protection, not only under the conditions of recognized bench tests, but also under the severe conditions of the MS Sequence 118 Engine Test. Furthermore, the ethoxylated amine composition combination with alkaline earth metal carbonate provides a pass under the very rigid specifications set forth by General Motors. in addition, the use of the compositions of poly(oxyalkylene) compounds permits smaller amounts of ash to be introduced into the oil and therefore avoids the problems associated with high ash oils. Finally, poly(oxyalkylene) additives are compatible with a wide range of other lubricating oil additives providing clear bright lubricant compositions.

I claim:

1. A lubricating oil composition comprising: a major amount of a hydrocarbon oil of lubricating viscosity; from about 0.01 to weight percent of at least one oilsoluble acid neutralization accelerating compound of the formula my R C-N- (R 0) R wherein R is an ethylene or propylene radical, a is an integer in the range of l to about 12, and R is an aliphatic hydrocarbon radical of molecular weight in the range from about to about 2,000; and sufficient alkaline earth metal carbonate dispersed in said hydrocarbon oil with a sulfonate or phenate dispersant to provide an alkalinity value of 0.5 to 100 ml KOH/g.

2. A composition according to claim 1 wherein said dispersant is a sulfonate dispersant derived from a sulfonic acid of from 25 to 50 carbon atoms.

3. A composition according to claim 1 wherein said dispersant is a phenate derived from alkylated phenol or polymerized alkylated phenols having 2 to 5 phenol groups per molecule and an alkyl group of from 12 to 30 carbon atoms.

Claims (3)

1. A LUBRICATING OIL COMPOSITION COMPRISING: A MAJOR AMOUNT OF A HYDROCARBON OIL OF LUBRICATING VISCOSITY; FROM ABOUT 0.01 TO 5 WEIGHT PERCENT OF AT LEAST ONE OIL-SOLUBLE ACID NEUTRALIZATION ACCELERATING COMPOUND OF THE FORMULA

2. A composition according to claim 1 wherein said dispersant is a sulfonate dispersant derived from a sulfonic acid of from 25 to 50 carbon atoms.

3. A composition according to claim 1 wherein said dispersant is a phenate derived from alkylated phenol or polymerized alkylated phenols having 2 to 5 phenol groups per molecule and an alkyl group of from 12 to 30 carbon atoms.