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Publication numberUS2280474 A
Publication typeGrant
Publication dateApr 21, 1942
Filing dateJul 18, 1938
Priority dateJul 18, 1938
Publication numberUS 2280474 A, US 2280474A, US-A-2280474, US2280474 A, US2280474A
InventorsGordon D Byrkit, Bert H Lincoln, Waldo L Steiner
Original AssigneeSocony Vacuum Oil Co Inc
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Lubricating oil
US 2280474 A
Abstract  available in
Images(7)
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Claims  available in
Description  (OCR text may contain errors)

ntt pr. It i 2,230,474 LUBBICATING OIL Gordon D. Byrklt, Waldo L. Steiner, and Bert E. Lincoln, Ponca City, Okla assignors, by mesne ascents, to Soeony-Vacuum Oil Company,

lncorporatcmNew York, N. Y... a corporation of New York No Drawing. Application Jluly it, rose, s No. new

M Claims.

Our invention relates to methods for the production oflubricating oils and specifically comprises such products as new compositions of matter.

The general trend in the development of internal combustion engines and particularly Diesel engines has imposed increasing demahds upon lubricating oils. These demands have required lubricants of greatly increased load carrying capacity, lubricants which may be used satisfactorily at higher temperatures of operation and lubricants more stable to the efiect or high temperatures and pressures under an oxidizing condition. The operating dimculties encountered with Diesel engines now being used represent these increased demands and the increas-' ing requirements being placed on lubricants. @ther types of internal combustion engines encounter the same dlfilculties in some duties and when employed for some services have encountered troubles similar to or identical with those occurring with Diesel engines.

some of these difllculties are sludge formation, stuck piston rings and the like. The term sludge as used in this specification includes various types of materials which are objectionable and that type of sludge which results in piston ring sticking. This in turn causes inadequate lubrication of the piston and cylinder walls and hence increased cylinder wear. Mild and severe scoring of the cylinder walls may occur and under severe conditions there may be actual seizure of the piston and cylinder by welding. Another consequence of ring sticking is blow-by which causes loss of power, increased consumption of fuel and lubricant for the same output and overheating of the piston and cylinder walls. Permanent distortion of the latter is a result of this overheating.

These dimculties cannot be overcome by changing the character of the hydrocarbon oil 56 amount of additive material.

itself. Mineral lubricating oils of one type, however, may not cause as much dimculty as oils or another type. In some cases, changes in refining processes will reduce the difiiculties to a certain extent, but it is commercially impractical and uneconomical to manufacture and distribute special lubricants from oil of a particular type and refined by a special and often expensive refining process. Generally speaking, the more 7 highly parafllnic lubricants which are us conceded to be superior lubricants are not as satisfactory as the naphthenic type lubricants for this specific purpose.

At least two special lubricants have been ofiered to solve the foregoing dimculties, but they have been found unsatisfactory and inadequate in many respects. One of these is a hydrocarbon lubricating oil to which has been added halogen bearing metal soaps, while the other is a blend of mineral oil with a small quantity of calcium soaps of aromatic substituted fatty acids. Both of these types of special lubricants have been found inadequate in the following respects:

l. Solubility.-Many of these addition, agents are not sufficiently soluble in hydrocarbon oils to give stable solutions containing the requisite This causes difflculty in the manufacture and distribution of these lubricants. If the amount of addition agent be reduced to that which will remain permanently in solution, it is insumcient to produce an appreciable improvement in the behavior or the oil even in normal use. This dificulty is sometimes partially overcome by the addition of a mutual solvent for both the soap and the hydrocarbon oil.-

2. To overcome this lack of solubility, free organic acids such as olelc, phenylstearic and the like may be added which increase the solubility of the soap in the oil. The added acid may be the same or different from the acid combined as soap. The addition of free acid to lubricants, however, precludes their use with many of the now common bearing metals especially those containing lead and cadmium because of the rapid corrosion of these metals by organic acids.

3. Efiectiveness.--Neither of the two types of additive materials has satisfactorily reduced the ring sticking dimculty. This failure may be due to'lack of stability or lack of solubility in sufiicient amounts to accomplish the purpose or both.

One object of our invention is to provide lubricants which will greatly reduce or substr tlally eliminate ring sticking in internal combustion engines, particularly those of the Diesel type.

Another object of our invention is to provide materials which when added to hydrocarbon oils will accomplish the same result.

A further object of our invention is to provide addition agents for lubricants which accomplish the above purposes and which are at the same time noncorrosive to the various metals encountered in internal combustion engines.

A still further object of our invention is to provide addition agents for lubricants which accomplish the above purposes and which are at the same time stable under the conditions of use and which do not accelerate the formation of any objectionable type of sludge.

Still another object of our invention is to provide addition agents for lubricants which will cause any sludge resulting from changes of the mineral oil during use to be of a soft, pliable. noncohesive and noncoherent type which will not interfere with normal operation.

Briefly, our invention consists of the addition to lubricants of small amounts, usually not over 5.0 percent, and more often of from 0.5 to 2.0 percent of certain metal salts or soaps of organic acids containing, in addition to the acid. group. also an ester grouping in the molecule. Most of the salts or soaps of the suitable metals with acids of the type described, namely acids having an ester group elsewhere in the molecule, are characterized by their ready solubility in mineral oils. This is a distinct advantage'in that blending of the additive agent with hydrocarbon oils is particularly easily accomplished and also in that there is no possibility of any separation of the added salt during storage or use. 'Calcium and other metal salts of fatty acids such as stearic and the like are not generally soluble to any appreciable. extent in mineral oils and are thus not suitable for the present use. Even the Salt of substituted fatty acids. while somewhat better in this respect than the unsubstituted compounds, are still far from being adequately soluble. The introduction of one or more ester groups greatly increases solubility in hydrocarbon oils.

Some lubricating oils exhibit better solvent power for these salts than others though the greater solubility obtained by changing the base oil is still small compared to the introduction of an ester group into the soap radical. In general, naphthenic base oils are better salt solvents than mixed or paraflln base oils of thesame viscosity.

By oil having lubricating characteristics in the appended claims, we means to include the socalled mineral oils and various hydrogenated, polymerized and otherwise synthetically treated oils such as volatilized oils and the like. Furthermore, the lubricating oil may consist in whole or in part of animal or vegetable oils such as castor oil, lard oil, shale oil, corn oil, cottonseed oil and the like.

The addition of organic acids to improve the solubility of metal soaps as disclosed in the prior art is not nearly as effective as we obtain by introduclng an ester group or groups into the molecule itself. It is a distinct improvement to have a soluble soap with the solubilizing agent a nonacidic group in the molecule of the soap itself.

The metals which we use to prepare our addition agents from the ester-acids include calcium, strontium, barium, zinc, cadmium, beryllium, aluminum, gallium, indium, thallium, iron, lead, copper, tin, germanium, mo ybdenum, bismuth, antimony, manganese, cobalt, nickel, chromium, and others. Some of the suitable metals listed above may form two or more types of salts or soaps depending on the valence of the metal. For example, we may use stannous or stannic salts. The salts of the same metal in diiferent valence states are often quite diflerent in solubility and suitability for special purposes. Thus salts of stannic tin appear to be better oxidation inhibitors than the corresponding stannous soaps. Plumbic lead soaps are more effective anti-knock agents when added to gasoline than the divalent lead soaps.

Some of these metals form salts or soaps which are more suitable than others for some purposes. Thus iron, lead, and copper soaps in general are found to be accelerators of oxidation in crankcase lubricants. While these are effective in reducing ring sticking, their other effect of accelerating oxidation renders them somewhat less desirable than other metal soaps in this particular service. On the other hand, the soluble lead soaps, for example, are quite desirable in the manufacture oi mild and violent types-of 'hypoid lubricants. Here the value or the extreme pressure characteristics of the soap far overshadows its oxidation accelerating ability. This is especially the case when we use a refined oil relatively difllcult to oxidize or add an oxidation inhibiting material or both.

In some cases, we may use metal salts of our ester-acids in which the metal is present as a complex ion. Thus the cobalt and nickel ions (trivalent) form complexes with the diamines such as ethylene and propylene diamines which may be used for preparing our salts. For example, tri (ethylene diamine) nickelic cetyl phthalate:

C HaNH:

and chloropentammine cobaltic cetyl amylene succinate:

ClCO (NHa) 5 (O.CO.CH2CH.C5H9CO2C10H31) 2 may be used.

The ester-acids which we use to prepare our addition agents are of two general types, both of which contain a carboxyl group (available for the preparation of the metal soap) and also an ester group. These are the partial esters of polybasic acids and the esters of hydroxy acids. These two types are characterized by the formulas: (a) HO2C.R.CO.O.R' and (b) HO2C.R.O.CO.R respectively, in which R is a divalent group and R is a monovalent group. The salts derived from esteriiied hydroxyacids of the type designated by formula (b) above constitute the subject matter of our copending application Serial 344,734, filed July 10, 1940, which is a continuation-ln-part of the present application. Compounds of these types are closely related and may even be isomeric, as in the case of monoheptadgcyl phthalate (l) and stearoyi salicylic acid both of which have the formula, C25H40O4.

We may also use salts or soaps of the partial esters of polybasic organic acids and of polyhydroxy compounds. Examples of these are shown later.

. The characterof R and R in the above eneral formulas may vary within wide limits since the solubilizing eiIect of the ester group is so powerful that it overcomes any diflicult solubility effect of R and R. Even radicals commonly thought to be insoluble in hydrocarbon oils may in some cases be used. The products, however, in which R and R contribute to solubility are particularly advantageous. R and R may be carbocyclic, heterocyclic or open chain and may or may not carry substituting groups such as nitrogen, halogens, sulfur, or phosphorus containing groups. Examples of these are shown below. It is to be understood that any of these substituting groups may be inserted in any of the specific compounds mentioned.

Dibasic acids and their derivatives, particularly the anhydrides, are used to prepare the halt esters to be converted into metal soaps. lPhthalic anhydride is an aromatic acid derivative suited to our purpose. Other satisfactory acids and their derivatives are terephthalic, naphthalic and the like. The condensation products oi the Diels and Alder type are particularly useful. For example, we may condense, by the method of Diels and Alder, maleic anhydride with a terp'ene hydrocarbon such as alpha-,

terpinene or the like to obtain a carbocyclic dibasic acid anhydride. Such a product is own to the art as 3-isopropyl-6-methyl-3,6-endoeth- 'ylene-Ai-tetrahydrophthalic anhydride. Other materials-which may be substituted for maleic anhydride in the Diels and Alder condensation include acrylic, methacrylic, cinnamic and crotonic acids and their derivatives among others. Acrolein is also useful. Other materials which may be substituted for the terpene'in the above example include cyclopentadiene, cyclohexadiene, anthracene, furane, fulvene, acids of drying and semidrying oils such as tung, linseed, cottonseed, corn, soy bean, rapeseed and the like, fish oil acids and partially hydrogenated fish oil acids, turpentine and any other materials containing conjugated double bonds such as dienes present in cracked gases and gasolines.

In preparing these condensation products from mono-basic acids such as acrylic or from nonacids such as acrolein, we choose an acid for the other addend so that the product will have at least two carboxyl groups or one carbonyl and one hydroxyl group. In this way, we may prepareour ester-acid for conversion into the metal soap.

some examples of the acids we may use in making our metal salts or soaps are:

I. Partial esters of polybasic acids A. Cyclic polybasic ac ds 1. With aliphatic alcohols, e.

a. Mono-octadecyl pht alate: (o) I'lO2C.CsH4.CO2C sH b. Monocetyl ihthalate:

(0) HOzC. nsHcCOzCitHti c. Monotctradccyl 3-clilorophthalatc (0) HOZC.CB}I3C].CO2CHHN d. Monolaiiryl naphthalate:

e. Monocetyl ester of the Diels-Alder condensation product of maleic anhydride with a torpcnc hydrocarbon: liozcdcizlflis-cozcuiptnu d Ditctra ecy pyrome iic aci f (iiOzClzCtHflCOiCuHnhH, 5) (HOzC)zCeH:(C02 u i0)i(2, Oz )zGoH2(C0iCn ii)i(2, a. Phosphite ofmono-fl-hydroxyethylphthalaie:

(HOQC.CQH4COCH1CH1O 3]? h. Monolauryl 8-nitrophthalate: HOzC.CcHaNOiCOzCi2His 2. With cyclic alcohols, c. g.: 1 a. Monobcnzyl phthalate:

(o) H02C.C6H4CO2CH2C6H5 b. Mono-fi-phenylethyl tercphthalate:

(D) HOzC.CaH|COiCHzCH:C5H5

c. Monofuriurylna hthalat/i:

B. Aliphatic polybasic acids:

1. With aligihatic alcohols, c. g.: a It onomyricyl mslcate:

H0zC.CH=CH.COiCaoHai b. Monodecyl amylenesuccinate:

H0aC.CHCHCsHoC0 C oH:| c. Monolauryl malatc:

HOZC-OHIOHOH.CUZCIIH25 Mono-B-hydroxyethyl chlorosucclnate: HOIC.CH:CHCLCOIOHICHIOH Monotetradecyl adipate HOgC.CHzCHrCHgCHaCOzCuHzo I. Monododec lmerca tosuccinate HOC.CH: HSH. OiCiiHii 2. With cyclic alcohols, e. g.:

a. Monobenz'yl succinat'e HO:C.CH1CH2CO2CH2COH6 b. Mono-B-phenylethyl tlilodiglycollatc HO C.CH;.S.CH:OO1CHzOHzQHs c. Monocinnamyl oxalate H0,C;CO;CHCH=CHCH5 C. Substituted polybasic acids:

1. With aliphatic alcohols, e. g.:

a. Mono (Z-ethyl hexyl) phenylsuccinate HO2C.CH2CHCOH5.CO:CH|CH(CzHb) I CHgCHgCHzCHa b. Mono-octadecyl phenylglutarate HOIC.CH2CH 2CHC5H5COOIEHE'I c. Monoootyl p-nitrophenylsuccinate H02o.CHiCHCsHlNOr-COzCmHII 2. With cyclic alcohols, e. 3.:

a. Mono-hydrocinnarnyl o-tolylsucciniite HOzC.CHzCH(CuH4CHal COICHiCHICHICOH b Mono-tctrahydrofurfuryl phenylsuccinste HOzC-CHzCHCsH5CO1C4H'IO c. Monto-B-phenylethyl o-aminophenylsuoci- II. Esters o! hydroxyacids A. Cyclic hydroxyacids 1. With aliphatic acids, 9. g.:

a. Stearoyl salicylic acid:

(o) HOqC.CoH4O.CO.Ci7Hu b. Trimyristoyl pyrogallic acid: (l)HOC;CH (O.C0.C1 Ha|)s(3,4,5l 2. With cyclic acids, e. g.:

a. Furoyl mandelic acid:

HOzC.CHC Hs.O.CO.CHaO b. Hydrocinnamoyl salicylic acid (o) H0 0.C,H.0.CO.CH=CH:C6H5 B. Aliphatic hydroryacids 1. With aliphatic acids, 0. g.:

a. Triinolecular selfmndensation product of lz-hydroxystearic acid HOzC(CH2)ioCH.CeHis O.C C(CHz) "ICU-Colin O.CO(CH2)|0CHOHC5H1J b. Stcarcyl l2-hydroxystearic acid HOiC(CHz)ioCHCaHii .C O.C :Ha5 2. With cyclic acids, 0. g.:

a. Monophthalyl amyl lactate (0) HOaC.C H4CO.O.CH(CHJ)COzCsHu b. Monophthalyl amyl citrate (O) HOzC.CsHiCO.0.C(COaCiHu) (CH COiCiHii): c. Diphthalyl amyl tartratc (o) (H010-C6H|C0.0.CH-CO2C5HH)1 d. Monotriphthalyl fi-chloroethylmalate (D) H010.C6H|.C0.0CH(OOICHSCHICI) cfla ozcHa fizcl Some examples of the metal salts or soaps which we prepare from these acids and blend with hydrocarbon oils to obtain our improved lubricants are:

1. Calcium octadecyl phthalate 2. Nickelous octadecyl phthalate 3. Chromic (III) octadecyl phthalate 4. Mercurous octadecyl phthalate Mercuric octadecyl phthalate Magnesium octadecyl phthalate Manganese (II) octadecyl phthalate Stannous octadecyl phthalate 9. Lead (II) amyl 3 -isopropyl-6-methyl-3,6- endoethylene-A4tetrahydrophthalate 10. Lead (II) cetyl-3-i.sopropyl-6-methyl-3,6-

endoethylene-Ae-tetrahydrophthalate ll. Stannic cetyl-3qisopropyl-6-methyl-3,6-endoethylene-A'i-tetrahydrophthalate 12. Barium soap of the monodecyl ester of the Diels and Alder condensation product of methacrylic acid with corn oil fatty acids.

cinnate Indium (III) stearoyl salicylate Thallous trimyristoyl pyrogallat Thallic furoyl mandelate Molybdenum hydrocinnamyl salicylate Manganous tris-hydroxystearate Manganic. stearoyl l2-hydroxystearate Nickel phthalyl amyl lactate Calcium cetyl p-aminophenylsuccinate Stannic tetradecyl mercaptosuccinate Lead A-hydroxyethyl phthalate phosphite Copper lauryl 3-nitrophthalate Calcium mono-octadecyl chlorophthalate Stannic monochloro-octadecyl phthalate Lead p-chlorobenzyl phthalate Stannous o-chlorobenzyl succinate Mercuric monocetyl chlorophthalate The quantities of our metal salts or soaps to be used may vary within wide limits depending on their relative effectiveness in accomplishing a certain desired result. As oxidation inhibitors in crankcase oils from 0.01 to 1.0 percent are generally eiiective. A blend of this composition has some beneficial effect on ring-sticking as compared with a hydrocarbon oil, but in order to obtain a sufficient efiect to be satisfactory more is usually required. Thus we may employ from 0.5 to ten percent in order to prevent ring sticking. It is obvious that this will vary depending on the ring sticking tendency of the base oil, the efliciency ot the addition agent,

temperature and other conditions of operation.

and the like We are not limited to a blend of hydrocarbon oil and a single metal soap but we may use more than one soap in the same blend. These mixed soaps may be heterogeneous with respect to the acid or metal or both. Thus we may use a blend of hydrocarbon oil, a small quantity of tin cetyl phthalate and a small quantity of calcium cetyl phthalate. In this case the mixed soaps are heterogeneouswith respect to metals. Another blend may contain besides the hydrocarbon oil small quantities of nickel octadecyl phthalate and nickel stea'royl-12-hydroxystearic acid. This blend is heterogeneous with respect to acid radicals in the soaps. One blend consists of hydrocarbon oil, stannic cetyl 3-isopro- ,pyl-6-me'thyl-3, 6-endoethylene-A-4 -tetrahydrophthalic anhydride. calcium stearoyl salicylate and lead (II) amyl 3-isopropyl-6-methyl-3, 6-endoethylene A4 tetrahyrophathallc anhydride. This blend is heterogeneous with respect to both acids and metals.

Our metal soaps may be used advantageously in combination'with lubricants 01' all kinds including those designed for use in automotive .Indium (II) tetrahydrofurfuryl phenylsucq crankcases, Diesel oils and any other oils of lubrieating viscosity. Furthermore our addends are advantageously blended in gasoline and other petroleum fuels either directly or after being blended first in a lubricating oil and then added to the fuel. Soap thickened lubricants, that is greases, are modified by the incorporation or varying amounts of our metal soaps. The ordinary soaps used in making greases may be replaced in whole or in only small part by certain of our metal soaps. These addends modify considerably the tackiness, penetration, resistance to breakdown by working or heat, and other properties of the greases. In making these greases, the usual soaps such as sodium stearate, aluminum stearate, calcium soaps of beta fat and the like may be used to form the large part of the necessary soap. Various other thickening ingredients or materials for other purposes may be added. These include yarn, hair, graphite, glycerol, water, lamp black, mica, zinc dust, etc.

It may be desirable to include in one and the same blend, in addition to the addends here described, other addends for specific purposes. Thus we may add a pour point depressor such as a naphthalene-clor-wax condensation product and a viscosity index improver such as certain resins or polymerized hydrocarbons in addition to our metal soaps of ester-acids. Furthermore, various other metallic compounds may be added to the bend without interfering with the action of our ingredients. Indeed, in some cases, it is advantageous to combine with our addends here described in a lubricating oil blend, such materials as calcium dichlorostearate, chromium oleate, aluminum stearate and other metallic soaps. We may also add various halogenated Q yEen-bearing ring or chain compounds including methyl dichlorostearate, lauryl trichloroacetal, chlorodiphenylene oxide, chlorodiphenvl ether and the like. Furthermore, sulfur-bearing materials may be added in the form of sulfurized methyl esters of corn oil acids, benzyl disulflde, alkyl polysulfides and the like. Examples of these are shown below.

The following examples of the preparation and use of the products of our invention are given for the purpose of illustration and not limitation:

Example 1 A mixture of 148 parts by weight of phthalic anhydride and 270 parts of octadecanol was heated at about C. for about two hours. The product was taken up in petroleum ether, filtered at room temperature, and the solvent evaporated from the filtrate. The resulting halt .ester of phthalic acid required 22 ml. of N/lO alkali to neutralize one gram. Theory, 24 ml.

Example 2 Example 3 A blend of 98.7 partsof a naphthenic base oil and 1.3 parts of the calcium octadecyl phthalate was tested in a Lauson engine which has been described in the literature of the art. While the oil alone showed two stuck rings at the end of fifteen hours, the blended 011 showed no stuck rings and a much cleaner piston. After thirty hours with the blended oil, one ring was partly Example 8 Percent Mid-Continent paraflln base S. A. E. 40.--- 98.0 Stannic octadecyl 3-isopropyl6'-methyl-3, 6-

stuck endoethylene-M-tetrahydrophthalate 0.2 v Chlorodlphenylene oxide; 1.8

Example 4 r A mixture of 702 'parts of the condensation Example 9 product of maleic anhydride with alpha-terping i t naphthenic ene and 768 parts of commercial cetyl alcohol'at a mum cetyl phthalate about 140 c. was heated for twenty hours. A clfigfwax-mphthalene condensatwn prod- 08 id 1 sh rter timeis robabl am 1e. I gggf g g honeymkexin w Sulfunzed methyl esters of corn oil acids 0.4 and soluble in mineral oils. It was less viscous, Example 10 however, than the original dibasic acid. For the manufacture of a grease we y use:

Example 5 Percent The acid-ester of Example 4 was vigorously Oleic acid stirred with water to which sufilcient ammonia Lime 1.1 was added to neutralize the acid when a thick Water o paste resulted. An excess of neutral calcium ace- Distillate '(460 seconds at 100 F.) 77.1 tate solution was added with vigorous stirring. Bright stock 12,0 The oily product was washed thoroughly with Calcium cetyl 3-isopropyl-6-methyl-3,6- 3222:1125? tdiet'i ani alali'iion Itlhelalstgllrierci updin peendoethylene-A4-tetrahydrophthalate 1,5 Grated 2 g 2 a1 g g It will be observed from these data that in the 6 methy1 3, 6 endoethylene MP tetrahydmpm case of the mercuric soaps, 0.1 percent of the thalate. This was an oil somewhat darker and octadgcyl phthalate produced afppmximately the more viscous than the acid ester of Examme 4. same lmprevement in the base oil as was produced It was miscible in all proportions with hydrocarby f the Phenylsteamesimilarly hon oils the stanmc octadecyl phthalate produced con.. slderably greater improvement than the stannic Example 6 oleate. The other metal soaps of octadecyl A blend of 15 parts of the calcium cetyl 3-iso- Phthalate showed appreciable ovement in pr py1..6-methy1 3 6.. 1 the oxidation characteristics of the mineral oil. dmphthalate of Example 5 and 985 parts of It wlllbe understood that certain features and Continent paraflin base oil, S. A. E. 30, was tested subcombmatmns are of utility and may be in the Lauson engine and showed at the end of ployed w referePce other features and a fifteen hour run a much cleaner piston and ensubcPmbmatmnsis ntemp19ited y and gine free of sludge as compared with a comparis wlthm the scope of our claims- It is further able run using the base oil without the soap. obvious P Various changes may be de in E Z 7 details within the scope of our claims without l 8 departing from the spirit of our invention. It is, The mono-octadecyl hth t of Example 1 therefore, to be understood that our invention is was neutralized with alcoholic potash and the not to be limited to the p fic de ails shown and tin soap precipitated by the addition or stannic bed. chloride, The soap was taken up in petroleum Having thus described our invention, we claim: ether and this solution washed, dried and evap- A lubricant comprising in fl bination a orated. major proportion of an oil having lubricating Blends of the'tin octadecyl phthalate of Examcharacteristics and a minor proportion of a metal ple 7 and others of our metal salts of ester-acids salt of an organic acid containing an ester group were made in a well-refined Mid-Continent elsewhere in the molecule. paraflin base oil of S. A. E. 30 and treated in the 2. A lubricant comprising in combination a well known Indiana oxidation test. The results major proportion of an oil having lubricating are compared in the following table wlth the base characteristics and a minor proportion of a metal oil and a corresponding blend of tin oleate and salt of a partial ester of a polybasic organic acid. mercury phenyl stearate for comparison. 3. A lubricant comprising in combination a Indiana test-hours to form Addend Amount Sludge 33} True color 10mg. mg. 0.5 1.0 1,000 2,000

Percent None (base oil) 15 50 10 9A 13 33 Mercuric phenylstearate 0.3 16 63 11 22 13 44 Mercurlc octadecyl phtllalate 0.1 15 52 8 22 16 28 Ollromlc octadecyl llthalate" 0.2 21 53 10 22 21 a0 Nickelous octadecy phthalate. 02 ll 04 s 20 2a 42 Menganous octadecyl phthalate 0.2 13 40 7 15 21 54 Barium oetadecyl pllthalate 0.2 20 56 17 84 27 51 Stem ea 0.2 18 or 11 2o 26 40 Btannic octadecyl phtllalate... 0.2 33 64 21 31 29 49 major proportion of an oil having lubricating characteristics and a minor proportion of a metal salt of a halt ester of a dibasic organic acid.

4. A lubricant comprising in combination an oil of lubricating characteristics and from 0.01 to 10 per cent of a metal salt of an organic acid containing an ester group elsewhere in the molecule.

5. A lubricant comprising in combination an oil having lubricating characteristics and from 0.1 to per cent of a metal salt of an organic acid containing an ester group elsewhere in the molecule.

6. A lubricant comprising in combination a major proportion of an oil having lubricating characteristics and a minor proportion of a metal salt of a partial ester of a polybasic acid which is prepared by condensing a polybasic acid containing conjugated double bonds with a material having the structure:

hydride of which is prepared by condensing a.

material containing conjugated double bonds with an anhydride of a dibasic acid having a double bond alpha, beta to the carboxyl group.

9. A lubricant comprising in combination a major proportion of an oil having lubricating characteristics and a minor proportion of a metal salt of a half ester of a dibasic acid formed by condensing a monobasic acid containing conjugated double bonds with a monobasic acid having a double bond alpha, beta to the carboxyl group.

10. A lubricant comprising in combination a major proportion of an oil having lubricating characteristics and a minor proportion of a metal salt of a partial ester oi a polybasic acid anhydride which is prepared by condensing a polybasic acid anhydride containing conjugated double bonds with a material having the struc-- ture:

11. A lubricant comprising in combination a major proportion of an oil having lubricating characteristics and a minor proportion of calcium cetyl 3-isopropyl-6-methyle3,6-endoethylene-A4- tetrahydrophthalate.

12. A lubricant comprising in combination'a major proportion of an oil having lubricating characteristics and a minor proportion of tin octadeoyl 3-isopropyl-6-methyl-3,6-endoethyJene- A4-tetrahydrophthalate.

13.-A lubricant comprising in combination a major proportion of an oil having lubricating 'cERTIFIGATiGFcGRRECTIOK. Patent No. 2,2 o-A7h. Apri1'2l, .19L 2.

GORDON D. BYRKIT, ET AL.

It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 5, sec- "ond column, line 52, for that portion of the formula reading (O0 CH CH Cl)' read "(00 613 63 01)": page h, first co1umn, -line'70, for "tetrahyrophathalic" read --tetrahydrophthalicand second column, line 51, for "bend" read --blend--; page 5, second column, line 29 for "improvement" rea'd --improvement--; and that the said Letters Patent should be read with this correction therein that. the same may conform to the record of the case in the Patent Office. 4

Signed and sealed this 7th day of Juiy, A. D. 19112.

Henry Van Arsdale, (Seal) Acting Commissioner of Patents.

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US2417833 *Apr 22, 1944Mar 25, 1947Continental Oil CoLubricant
US2469003 *Jul 14, 1947May 3, 1949Gulf Research Development CoLubricating oil compositions
US2595169 *Jan 25, 1946Apr 29, 1952Standard Oil Dev CoSteam turbine lubricants
US2809161 *Dec 29, 1955Oct 8, 1957California Research CorpLubricant composition
US2810696 *Dec 29, 1955Oct 22, 1957California Research CorpLubricant composition
US2900339 *Mar 13, 1958Aug 18, 1959California Research CorpProcess for preparing lubricant compositions and concentrates therefor
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