US2308116A - Pour point depressant for lubricating oils - Google Patents
Pour point depressant for lubricating oils Download PDFInfo
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- US2308116A US2308116A US344912A US34491240A US2308116A US 2308116 A US2308116 A US 2308116A US 344912 A US344912 A US 344912A US 34491240 A US34491240 A US 34491240A US 2308116 A US2308116 A US 2308116A
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/06—Groups 3 or 13
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/08—Groups 4 or 14
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/12—Groups 6 or 16
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/14—Group 7
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/16—Groups 8, 9, or 10
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Definitions
- the metal stearate should be soluble in hydrocarbon oil and the valence of pour point depressants for lubriconvenient source for such a combination or mixture of sulphonated petroleum hydrocarbons is furnished by the so-termed' fmahogany petroleum sulphonic acids obtained in the acid refining of petroleum oil distillateswith concentrated and preferably fuming sulphuric acid under sulphonating conditions of acid concentration and temperature, and isolated from the pe troleum oil layer, after the separation of the acid sludge, in the form of their salts, i. e., ma-
- oil soluble metal pee troleum sulphonates are,for instance,the sodium; potassium, magnesium, zinc, nickel, cobalt, cadmium, tin, chromium, and aluminum sulphonates.
- Ammonium sulphonates may also be used though their addition is not recommended inmany cases on account of their heat instability which may its metal radical should be at least two and preferably three.
- metalllc soap pour point depressant of the stearate type or where an expressionof similar import is used, it is intended to designate thereby any oil-soluble metallic soap, such as a palmitate, stearate, oleate or the like, capable of depressing the pour point of a waxy lubricating oil, the normal relatively high pour point of which is due to the. wax contained therein, and typified by the conventionally used oil soluble metal stearates and particularly aluminum stearate.
- the oil soluble petroleum sulphonate that may be used within the purview of myinvention may be any one or more of the oil soluble metal sulphonates derived from the sulphonation of petroleum hydrocarbons.
- the oil soluble sulphonate may constitute either an individual sulphonated petroleum hydrocarbon or a mixture or combination of said sulphonated petroleum hydrocarbons. I prefer, however, to-use as the oil soluble sulphonate in accordance with my invention, a combination or mixture of-such sulphonated petroleum hydrocarbons.
- the tin, cobalt and cadmium petroleum sulphonates have the added advantage that they will impart. to an appreciable degree, anti-corrosive properties to any hydrocarbon oil product containing the same.
- the depressant in accordance with the invention may be conveniently prepared by intimately mixing a conventional metallic soap depressant with the required amount of oil soluble petroleum sulphonate.
- a ratio of metallic soap such as stearate to sulphonate from 10:1 to 2:1, the latter being the most efficient proportion; although the amount of sulphonate present in. the lowest effective ratio of metallic soap to sulphonate of 10:1 is relatively .small it nevertheless sufilces to substantially eliminate any reversion of v the pour point of thewaxy hydrocarbon oil.
- the oil soluble petroleum sulphonate may be used either as such, that is, in substantially'dry able solvent such as a petroleumhydrocarbon oil.
- a suitable oil-and preferably in what is termed retained oil" as such solution is the conventional product ordinarily and conveniently obtained in the manufacture of these substances.
- oil soluble petroleum sulphonate or any term of similar import connotes generically any one or more oil soluble metal salts of a sulphonated hydrocarbon or mixture of hydrocarbons within the petroleum hydrocarbon range and irrespective of whether the same is a mahogany petroleum sulphonate compound or fraction thereof, or not.
- the pom-point measurements of the untreated oil were carried out as prescribed by the well known ASTM test for thedetermination of pour point, designated as D9'7-39.
- the revision data recited in'the foregoing table were obtained by storing the oil at 32 F. and observing the temperature at which the oil loses fluidity after the indicated time intervals.
- the metallic soap-petroleum sulphonate depressant in accordance with the invention may be added to the waxy hydrocarbon oil, the pour point of which is to be depressed either as such, 1. e., in substantially dry form, or in the form of a concentrated base in a suitable carrier.
- the latter method is conventionally practiced inconnection with the use of pour point depressants generally and offers certain. advantages ease of handling and of distribution in .the oil 75 normally gel forming amounts (1.
- a lubricating oil distillate under sulpho-- such as 'rier it is as a rule preferred to select as the carrier a suitable hydrocarbon oil and preferably a hydrocarbon oil of the lubricating oil distillate range.
- a suitable hydrocarbon oil and preferably a hydrocarbon oil of the lubricating oil distillate range.
- a depressant containing, in addition to the metallic soap or mixture-of metallic soaps, a suitable oil soluble petroleum sul phonate, the afore-described-disadvantages are substantially eliminated and the base or-concentrate, substantially comprising a solution of the metallic soap-sulphonate-depressant is substantially free from gel formation.
- the volume of the hydrocarbon oil carrier is such that it is at least sumcient to wet the entire amount of oil soluble metallic soap, such-as a metal stearate, and dissolve the oil soluble petroleum sulphonate.
- oil carrier Approximately 30% of oil carrier will sufilcevin most cases for-this purpose. In many instances it is of advantage to use as the carrier that petroleum hydrocarbon oil to which the base or concentrate containing the depressant is to be added for the purpose of reducing its pour point.
- the petroleum sulphonate component of the base When usinggas the petroleum sulphonate component of the base a mixture of sulphonates obtained from the acid treatnating conditions as before described and containing retained oil, the latter may serve as the carrier, thus eliminating the necessity'for further hydrocarbon oil addition to the base. In the majority of cases it is preferred to use in excess of 30% and preferably between 45 and 94% petroleum hydrocarbon oil carrier (by weight) for the base.
- the oil soluble metal soap should be present in the hydrocarbon oil carrier to an appreciable extent, and preferably at least in, or in excess of,
- oilcarrier may, however, range from as low as 1% to as high as 48%. In most cases, depending upon the amount and type of.
- oil soluble metallic soap used in the base amounts of between 2% and of oil soluble Petroleum sulphonate content are recommended for the base.
- Tables-II and 1H illustrate the pour pointreduction of various Pennsylvania paraffin base oils after the addition, of the metallic soap-petroleum sulphonate depressant in accord ance with the invention.
- Table II shows various parafim base oils of substantially the same stearate and sulphonate content, i.- e., approximately .12 aluminum stearate and .04%
- a lubricating oil composition of relatively low, substantially non-fugitive; non-reverting pour point comprising a wax-containing petroleum hydrocarbon oil having normally a relatively high pour point due to the wax contained therein,- a polyvalent metal stearates pour point depressant in amount and potency sufficient to lower said pour point and an oil'soluble metallic petroleum sulphonate, said sulphonate and said soap being present in a ratio of 1:10 to 1:2.
- a lubricating oil composition of relatively ow, substantially non-fugitive, non-reverting pour point comprising a wax-containing petroleum hydrocarbon oil having normally a relatively high pour point due to the wax contained therein, approximately .01 to .5% polyvalent metal stearates pour point depressant for such oil and approximately .001 to .25% oil soluble metallic petroleum sulphonate.
- a lubricating oil composition of relatively low, substantially nonfugitive, non-reverting pour point comprising a wax-containing petroleum hydrocarbon oil having normally a relatively highpour point due to the wax contained therein, approximately .1 to .25% polyvalent metal stearates pour point depressant for such difiering stearate and mahogany sulphonate content, the minimum absolute depression of the pour point of each oil being 10 Table II Pennsylvania parali'm base oil (con- Normal Reduced Absolute taming .127 Al stearate-.0691. pour pour depres- Nalvlahsulphonate) point point sion 1; I S. A. E. 25 -30 55 S. A. E. 20. 25 20 S. A. E.
- a lubricating oil composition in accordance with claim 3 in which said metallic soap depressantiis aluminum stearate and in which said oil soluble petroleum sulphonate is tin petroleum mahogany sulphonate.
- a lubricating oil composition comprising a wax-containing petroleum hydrocarbon oil of normally high pour point and small quantities oi at least one soap having pour point depressing properties selected from the group consisting of polyvalent metal stearates, andpalmitates, and
- an oil soluble metallic petroleum sulphonate said soap being present in amount and potency sufiicient to lower said pour point at least 10 F.
- a lubricating oil composition comprising a wax-containing petroleum hydrocarbon oil of normally high pour point and small quantities of aluminum stearate in amount and potency sufllcient to lower said pour point at least 10 F. and an oil soluble metallic petroleum sulphonate.
- a lubricating oil compositionof relatively low, substantially non-fugitive, non-reverting pour point comprising a wax-containing petroleum hydrocarbon oil, having normally a relatively high pour point due-to the wax contained therein, a metallic soap pour point depressant composedof at least one member selected from the group consisting of polyvalent metal stearates and palmitates in amount and potency sufiicient to lower said pour point at least 10 F., and an oil soluble metallic petroleum sulphonate, said sulphonate and said soap being present in a ratio of at least 1:10.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
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- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Jan. 12, 1943 UNITED STATES. PATENT POUR'POINT DEPBESSANT LUBRICATING OILS OFFICE roa Isador Silvernian, Newark, N. 1., assign'or to L.
Sonneborn Sons, Inc.
ware
No Drawing. Application uly 11, 1940, i
, a corporation of Dela- Serial No. 344,912
8 Claims. (01. 252 36) high pour point due to the wax contained therein. The use of these depressants, however is attended by the disadvantage that thepour point obtained is substantially fugitive and reverts upon storageor in service progressively towards the pour point of the original undepressed oil.
I have discovered that-this disadvantage may be overcome and that a substantially permanent lowering of the pour point and a substantially non-fugitive, non-reverting pour point may be obtained by admixing withthe oil a metallic soap depressant in the presence of an oil soluble petroleum sulphonate.
The metal stearates conventionally used as pour point depressants, and particularly the tin, titanium, calcium, magnesium and aluminum stearates, constitute satisfactory depressants in accordance with the invention. They may be used either singly or in mixture with one another; Though the use of one or the other particular stearate may be recommended by special circumstances or considerations, as for instance, the use of tin stearate in cases where anti-corrosive properties are desired, the use of aluminum stearate in most .instances is the preferred practice. The metal stearate should be soluble in hydrocarbon oil and the valence of pour point depressants for lubriconvenient source for such a combination or mixture of sulphonated petroleum hydrocarbons is furnished by the so-termed' fmahogany petroleum sulphonic acids obtained in the acid refining of petroleum oil distillateswith concentrated and preferably fuming sulphuric acid under sulphonating conditions of acid concentration and temperature, and isolated from the pe troleum oil layer, after the separation of the acid sludge, in the form of their salts, i. e., ma-
- hogany petroleum sulphonatesor oil soluble petroleum sulphonates in accordance with well--v known practices. Suitable oil soluble metal pee troleum sulphonates are,for instance,the sodium; potassium, magnesium, zinc, nickel, cobalt, cadmium, tin, chromium, and aluminum sulphonates. Ammonium sulphonates may also be used though their addition is not recommended inmany cases on account of their heat instability which may its metal radical should be at least two and preferably three. v 7
Where in the specification and claims. reference is made to the term metalllc soap pour point depressant of the stearate type or where an expressionof similar import is used, it is intended to designate thereby any oil-soluble metallic soap, such as a palmitate, stearate, oleate or the like, capable of depressing the pour point of a waxy lubricating oil, the normal relatively high pour point of which is due to the. wax contained therein, and typified by the conventionally used oil soluble metal stearates and particularly aluminum stearate. I
The oil soluble petroleum sulphonate that may be used within the purview of myinvention may be any one or more of the oil soluble metal sulphonates derived from the sulphonation of petroleum hydrocarbons. The oil soluble sulphonate may constitute either an individual sulphonated petroleum hydrocarbon or a mixture or combination of said sulphonated petroleum hydrocarbons. I prefer, however, to-use as the oil soluble sulphonate in accordance with my invention, a combination or mixture of-such sulphonated petroleum hydrocarbons. The most entail the formation of deleterious free acidity. In the majority of cases, however, the tin and aluminum sulphonates are preferred. The tin, cobalt and cadmium petroleum sulphonates have the added advantage that they will impart. to an appreciable degree, anti-corrosive properties to any hydrocarbon oil product containing the same.
For best results I have found it of advantage and prefer to use an oil soluble petroleum sulphonate that has been substantially freed from inorganic impurities and free organic acidity. Though I preferably use in accordance with my invention a combination or mixture of sulphonated, compounds obtained from mahogany petroleum sulphonic acid or their salts, it ispossible and sometimes of advantage to use as the oil soluble petroleum sulphonate in. accordance with the invention, one or more fractions or component ingredientsof the mahogany petroleum sulphonates. I
The depressant in accordance with the invention may be conveniently prepared by intimately mixing a conventional metallic soap depressant with the required amount of oil soluble petroleum sulphonate. In most cases I prefer a ratio of metallic soap such as stearate to sulphonate from 10:1 to 2:1, the latter being the most efficient proportion; although the amount of sulphonate present in. the lowest effective ratio of metallic soap to sulphonate of 10:1 is relatively .small it nevertheless sufilces to substantially eliminate any reversion of v the pour point of thewaxy hydrocarbon oil.
. The oil soluble petroleum sulphonate; may be used either as such, that is, in substantially'dry able solvent such as a petroleumhydrocarbon oil. When using mahogany petroleum'sulphonate in accordance with the inventiomI prefer a solution in a suitable oil-and preferably in what is termed retained oil" as such solution is the conventional product ordinarily and conveniently obtained in the manufacture of these substances.
The expression oil soluble petroleum sulphonate or any term of similar import, as employed in the specification and claims, connotes generically any one or more oil soluble metal salts of a sulphonated hydrocarbon or mixture of hydrocarbons within the petroleum hydrocarbon range and irrespective of whether the same is a mahogany petroleum sulphonate compound or fraction thereof, or not.
For the purpose of depressing the pour point of a parafiin base oil such as a Pennsylvania grade oil, so much of the depressant prepared in accordance with the invention is added thereto as is equivalent to an amount of oil soluble metallic soap sufiicient to appreciably reduce the pour point of the oil and preferably reduce the same at least 10 below its normal pour point. Depending upon the viscosity of the oil, an amount equivalent to yield in the depressed oil at least ,01% to 25% metallic soap, such as aluminum stearate, will usually suffice. It is generally preferred, however, to procure maximum depression of pour point for a given oil and, in most cases, depending upon the viscosity of the oil, approximately .1% to .5% metallic soap such as aluminum stearate will produce such result.
In the following Table I a series of pour point reversion tests are tabulated for an SAE 10 and an SAE 40 oil respectively. In both cases the oil depressed with aluminum stearate alone showed an absolute reversion after 168 hours, in one case of 60 and in the other case of 35, whereas in I both instances the reversion of the pour point of the oil containing sodium mahogany sulphonate was zero.
Table I Reversion Pour point F. afterdepressed pour pcintF. Mill-s. 481m. 72hrs. l68hrs.
S. A. E. 10 Penn. grade oil original pour point +25 F.:
Aluminum stea- -30 t -25 -10 +25 rate alone. q Y Aluminum stea- -30 -30 -30 30 25 rate sodium mahogany: sulphonate. S. A. E. 40 Penn. grade oil original pour point +25 F.:
Aluminum stea- '-l0. -5 0 +25 ra Aluminum steal0 -l0 lo --10 -l0 rate+sodium mahogany sulphonate.
The pom-point measurements of the untreated oil were carried out as prescribed by the well known ASTM test for thedetermination of pour point, designated as D9'7-39. The revision data recited in'the foregoing table were obtained by storing the oil at 32 F. and observing the temperature at which the oil loses fluidity after the indicated time intervals.
The metallic soap-petroleum sulphonate depressant in accordance with the invention may be added to the waxy hydrocarbon oil, the pour point of which is to be depressed either as such, 1. e., in substantially dry form, or in the form of a concentrated base in a suitable carrier. The latter method is conventionally practiced inconnection with the use of pour point depressants generally and offers certain. advantages ease of handling and of distribution in .the oil 75 normally gel forming amounts (1.
' ment of a lubricating oil distillate under sulpho-- such as 'rier, it is as a rule preferred to select as the carrier a suitable hydrocarbon oil and preferably a hydrocarbon oil of the lubricating oil distillate range. When adding the metallic soap-sulphonate depressant in substantially dry form to the waxy hydrocarbon oil, it is preferred to accomplish the addition while the oil is hot.
The preparation of a metallic soap depressant base or concentrate has in the past offered a variety of disadvantages, foremost among which has been the occurrence of gel formation in the base as the consequence of peptization resulting in the partial or total loss of homogeneity of the base when comparatively large amounts of soap are present. For the purpose of preserving at least some degree of homogeneity it has been hitherto necessary to materially reduce the metallic soap concentration of the base and even then peptization of the gels formed upon-storage results in the formation of a precipitate of substantially undissolved discrete soap particles. When preparing a depressant, however, in accordance'with the invention, 1. e., a depressant containing, in addition to the metallic soap or mixture-of metallic soaps, a suitable oil soluble petroleum sul phonate, the afore-described-disadvantages are substantially eliminated and the base or-concentrate, substantially comprising a solution of the metallic soap-sulphonate-depressant is substantially free from gel formation. The gel formation in the base or concentrate isto such an extent suppressed that, whereas inthe past a maximum of but approximately three to four percent of a metallic soap, such as aluminum stearate, was capable of solution by the hydrocarbon oil carrier, and only then with the aid of a suitable gel breaking material, it is now possible to dissolve in the presence of the oil soluble petroleum sulphonate as high as 48% and sometimes even higher amounts of a suitable metallic soap in the hydrocarbon oil carrier. Thus the production of a pour point depressant base or concentrate is possible which is approximately twelve times as powerful as could hitherto be obtained.
when usingthe metallic soap-petroleum sulphonate depressant in accordance with the invention in the form of a base, it is desirable that the volume of the hydrocarbon oil carrier is such that it is at least sumcient to wet the entire amount of oil soluble metallic soap, such-as a metal stearate, and dissolve the oil soluble petroleum sulphonate. Approximately 30% of oil carrier will sufilcevin most cases for-this purpose. In many instances it is of advantage to use as the carrier that petroleum hydrocarbon oil to which the base or concentrate containing the depressant is to be added for the purpose of reducing its pour point. When usinggas the petroleum sulphonate component of the base a mixture of sulphonates obtained from the acid treatnating conditions as before described and containing retained oil, the latter may serve as the carrier, thus eliminating the necessity'for further hydrocarbon oil addition to the base. In the majority of cases it is preferred to use in excess of 30% and preferably between 45 and 94% petroleum hydrocarbon oil carrier (by weight) for the base. I
The oil soluble metal soap should be present in the hydrocarbon oil carrier to an appreciable extent, and preferably at least in, or in excess of,
e., at least, or in.
stearate .in the oilcarrier may, however, range from as low as 1% to as high as 48%. In most cases, depending upon the amount and type of.
oil soluble metallic soap used in the base, amounts of between 2% and of oil soluble Petroleum sulphonate content are recommended for the base.
Where in the specification and claims reference quired and will remairrsubstantially fluid and non-gel forming in storage.
When a baseor concentrateprepared in accordance with the invention 'contains'approximately 4% aluminum stearate, 2% sodium mahogany sulphonate and 94% carrier oil, of which 06-03% is retained oil, an addition of approximately 3% of thisbase or-concentrate to a Pennsylvaniaparaflin base-oil will-yield therein a stearate contentof approximately 0.12% and a sulphonate content of approximately 0.04%.
The following Tables-II and 1H illustrate the pour pointreduction of various Pennsylvania paraffin base oils after the addition, of the metallic soap-petroleum sulphonate depressant in accord ance with the invention. Whereas Table II shows various parafim base oils of substantially the same stearate and sulphonate content, i.- e., approximately .12 aluminum stearate and .04%
. sodium mahogany sulphonate, TablealII illustrates various Pennsylvania paraffin bas'e oils of hogany sulphonate which progressively reverted to normal. v
The foregoing description is -for purposes of illustration and not of limitation, and is not to be limited except by the appended claims in which I have endeavored to claim broadly all inherent novelty.
I claim:
1. A lubricating oil composition of relatively low, substantially non-fugitive; non-reverting pour point comprising a wax-containing petroleum hydrocarbon oil having normally a relatively high pour point due to the wax contained therein,- a polyvalent metal stearates pour point depressant in amount and potency sufficient to lower said pour point and an oil'soluble metallic petroleum sulphonate, said sulphonate and said soap being present in a ratio of 1:10 to 1:2.
2. A lubricating oil composition of relatively ow, substantially non-fugitive, non-reverting pour point comprising a wax-containing petroleum hydrocarbon oil having normally a relatively high pour point due to the wax contained therein, approximately .01 to .5% polyvalent metal stearates pour point depressant for such oil and approximately .001 to .25% oil soluble metallic petroleum sulphonate.
,3. A lubricating oil composition of relatively low, substantially nonfugitive, non-reverting pour point comprising a wax-containing petroleum hydrocarbon oil having normally a relatively highpour point due to the wax contained therein, approximately .1 to .25% polyvalent metal stearates pour point depressant for such difiering stearate and mahogany sulphonate content, the minimum absolute depression of the pour point of each oil being 10 Table II Pennsylvania parali'm base oil (con- Normal Reduced Absolute taming .127 Al stearate-.0691. pour pour depres- Nalvlahsulphonate) point point sion 1; I S. A. E. 25 -30 55 S. A. E. 20. 25 20 S. A. E. 30 25 l() 35 S. A. E. 40. ---25 --l() 35 S. A. E. 50. '25 0 25 Table III I Pennsylvaniaparallin base oil NaMah. s;A. E. safe. s. A. E. s. A. E. mate sulphonate s A E on 30 4o I Depression pour point The depressed pour point obtained in each of the oils listed in Tables II and III was free from reversion as compared with the pour point of the same oils containing the same aluminum stearate content but without the addition of the maoil and approximately .01 to oil soluble metallic petroleum sulphonate.
4. A lubricating oil composition in accordance with claim 3 in which said metallic soap depressant is aluminum stearate and in which said oil soluble petroleum sulphonate is alkali petroleum mahogany sulphonate. i
5. A lubricating oil composition in accordance with claim 3 in which said metallic soap depressantiis aluminum stearate and in which said oil soluble petroleum sulphonate is tin petroleum mahogany sulphonate.
6. A lubricating oil composition comprising a wax-containing petroleum hydrocarbon oil of normally high pour point and small quantities oi at least one soap having pour point depressing properties selected from the group consisting of polyvalent metal stearates, andpalmitates, and
an oil soluble metallic petroleum sulphonate, said soap being present in amount and potency sufiicient to lower said pour point at least 10 F.
7. A lubricating oil composition comprising a wax-containing petroleum hydrocarbon oil of normally high pour point and small quantities of aluminum stearate in amount and potency sufllcient to lower said pour point at least 10 F. and an oil soluble metallic petroleum sulphonate.
8. A lubricating oil compositionof relatively low, substantially non-fugitive, non-reverting pour point comprising a wax-containing petroleum hydrocarbon oil, having normally a relatively high pour point due-to the wax contained therein, a metallic soap pour point depressant composedof at least one member selected from the group consisting of polyvalent metal stearates and palmitates in amount and potency sufiicient to lower said pour point at least 10 F., and an oil soluble metallic petroleum sulphonate, said sulphonate and said soap being present in a ratio of at least 1:10.
ISADOR SILVERMAN.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US344912A US2308116A (en) | 1940-07-11 | 1940-07-11 | Pour point depressant for lubricating oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US344912A US2308116A (en) | 1940-07-11 | 1940-07-11 | Pour point depressant for lubricating oils |
Publications (1)
Publication Number | Publication Date |
---|---|
US2308116A true US2308116A (en) | 1943-01-12 |
Family
ID=23352628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US344912A Expired - Lifetime US2308116A (en) | 1940-07-11 | 1940-07-11 | Pour point depressant for lubricating oils |
Country Status (1)
Country | Link |
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US (1) | US2308116A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2415353A (en) * | 1944-03-15 | 1947-02-04 | Standard Oil Dev Co | Rust preventing turbine oil |
US2416192A (en) * | 1943-02-20 | 1947-02-18 | Union Oil Co | Petrolatum sulfonate |
US2423789A (en) * | 1944-06-01 | 1947-07-08 | Sonneborn Sons Inc L | Pour point depressants for lubricating oils |
US2438461A (en) * | 1944-08-03 | 1948-03-23 | Standard Oil Dev Co | Cutting oil composition |
US2458034A (en) * | 1946-11-20 | 1949-01-04 | Standard Oil Co | Mineral castor oil |
US2467836A (en) * | 1945-08-04 | 1949-04-19 | Standard Oil Dev Co | Lubricants |
US4261841A (en) * | 1979-12-18 | 1981-04-14 | Phillips Petroleum Company | Lubricating composition comprising hydrogenated oligomers of 1,3-diolefins and a calcium petroleum sulfonate |
-
1940
- 1940-07-11 US US344912A patent/US2308116A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2416192A (en) * | 1943-02-20 | 1947-02-18 | Union Oil Co | Petrolatum sulfonate |
US2415353A (en) * | 1944-03-15 | 1947-02-04 | Standard Oil Dev Co | Rust preventing turbine oil |
US2423789A (en) * | 1944-06-01 | 1947-07-08 | Sonneborn Sons Inc L | Pour point depressants for lubricating oils |
US2438461A (en) * | 1944-08-03 | 1948-03-23 | Standard Oil Dev Co | Cutting oil composition |
US2467836A (en) * | 1945-08-04 | 1949-04-19 | Standard Oil Dev Co | Lubricants |
US2458034A (en) * | 1946-11-20 | 1949-01-04 | Standard Oil Co | Mineral castor oil |
US4261841A (en) * | 1979-12-18 | 1981-04-14 | Phillips Petroleum Company | Lubricating composition comprising hydrogenated oligomers of 1,3-diolefins and a calcium petroleum sulfonate |
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