US2367435A - Compounded oil and process of preparing the same - Google Patents
Compounded oil and process of preparing the same Download PDFInfo
- Publication number
- US2367435A US2367435A US471894A US47189443A US2367435A US 2367435 A US2367435 A US 2367435A US 471894 A US471894 A US 471894A US 47189443 A US47189443 A US 47189443A US 2367435 A US2367435 A US 2367435A
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- United States
- Prior art keywords
- acids
- oil
- soaps
- alkaline earth
- sulphonic acids
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 14
- 230000008569 process Effects 0.000 title description 3
- 239000002253 acid Substances 0.000 description 70
- 150000007513 acids Chemical class 0.000 description 64
- 239000000344 soap Substances 0.000 description 53
- 239000003921 oil Substances 0.000 description 37
- 239000010687 lubricating oil Substances 0.000 description 26
- 239000003208 petroleum Substances 0.000 description 22
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 19
- 150000001342 alkaline earth metals Chemical class 0.000 description 17
- 239000012286 potassium permanganate Substances 0.000 description 16
- 239000000314 lubricant Substances 0.000 description 9
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 7
- 238000002485 combustion reaction Methods 0.000 description 7
- 229910052748 manganese Inorganic materials 0.000 description 7
- 239000011572 manganese Substances 0.000 description 7
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 6
- 229910052791 calcium Inorganic materials 0.000 description 6
- 239000011575 calcium Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000000470 constituent Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 241000158728 Meliaceae Species 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000011550 stock solution Substances 0.000 description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 4
- 239000001117 sulphuric acid Substances 0.000 description 4
- 235000011149 sulphuric acid Nutrition 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- -1 for example Substances 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 239000011147 inorganic material Substances 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 150000003460 sulfonic acids Chemical class 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- 229920000136 polysorbate Polymers 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- WIKSRXFQIZQFEH-UHFFFAOYSA-N [Cu].[Pb] Chemical compound [Cu].[Pb] WIKSRXFQIZQFEH-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 239000010710 diesel engine oil Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- LBSANEJBGMCTBH-UHFFFAOYSA-N manganate Chemical compound [O-][Mn]([O-])(=O)=O LBSANEJBGMCTBH-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- 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
- C10N2010/04—Groups 2 or 12
Definitions
- This invention relates to improvements in lubricating oils and has for a principal object the provision of a lubricating oil having superior non-sludging characteristics when employed under the conditions of high temperature and pressure met in internal combustion engines.
- Another object of the invention is to provide a lubricant which is non-corrosiveto the metal surfaces of an engine, especially to alloy bearmgs.
- a further object is the purification of sulphonic acids and sulphonic soaps to render the same more suitable for use as additives to lubricating oils.
- sulphonic acids derived from petroleum oils by treatment with concentrated sulphuric acid contain certain impurities which are the chief source of the corrosiveness generally experienced when their soaps are compounded with lubricating oils. If these impurities are removed or converted to non-corrosive compounds, the major portion'of the sulphonic acids produce alkaline earth soaps especially adapted for use in lubricating oils and oils blended with alkaline In the earth soaps of such purified sulphonic acids have vproven to be effective to a very high degree.
- the liquid lubricant comprises a body of petroleum lubricating oil which contains dissolved alkaline earth metal soaps of the more stable constituents of petroleum sulfonic acids and alkaline earth metal soaps of the oxidation products of less stable constituents of petroleum sulfonic acids.
- crude sulphonic acids derived from mineral oils are treated with potassium permanganate, preferably in an acidified aqueous solution, for a sumcient time to oxidize the more unstable compounds in the acids.
- potassium permanganate in an amount equal'to approxi mately 0.01 to 0.5 equivalent weight per molecule of sulphonic acid is used, but in most cases best results are obtained when using from about, 0.1 to 0.2 equivalent weight.
- equivalent weight of potassium permanganate is 31.6, a batch of 400 pounds of sulphonic acids having an average molecular weight of 400 (i.
- one pound-mole of sulphonic acids may be treated with as little as 0.3 pound of potassium permanganate with noticeable effect, or the batch may be treated with as much as about 16 pounds of potassium permanganate without obtaining any considerable amount of deleterious reactions with the excess permanganate.
- permanganate to oxidize the more unstable components of the crude sulphonic acids and the exact quantity of permanganate for best results in each individual case may readily be determined by a skilled chemist by simple tests.
- an ordinary glazed or lead lined a itator equipped with means for mechanical or air agitation is suitable.
- various types of batch or continuous contacting apparatus may be used.
- the reaction of the potassium permanganate with the unstable components may be. carried out; in various media, or even with dry permanganate by far the most satisfactory method is by contacting the sulphonic acids with the peracidified with a small amount of strong acid such as, for example, sulphuric acid. Care should be taken, of course, not to bring the permanganate into contact with concentrated strong acid, especially concentrated sulphuric acid, due to the danger of forming explosive mixtures.
- With efficient contacting the reaction of the potassium permanganate with the crude sulphonic acids takes place quite rapidly and, at ordinary temperatures, the reaction is nearly complete in several minutes. However, the reaction may be speeded up by applying a moderate degree of heat. For this purpose excellent results have been obtained using temperatures from 100 F.
- the sulphonic acids are emulsified to a greater or less extent with the water present. They may be separated therefrom by the addition of some solvent such as alcohol or gasoline, the former uniting with the water of the emulsion and the latter uniting with the sulphonic acids. In either case two layers are formed, the non-aqueous layer containing the sulphonic acids.
- the sulphonic acids are then freed from any solvent and converted to calcium or other alkaline earth soaps by treatment withlime or with the hydroxide of magnesium, strontium, or barium, or in any other desired manner, such as for example, first forming the sodium soaps and converting these to the alkaline earth soaps by treatment with suitable alkaline earth metal salt.
- the emulsion of purified sulphonic acids and water may be treated with lime or other alkaline earth metal hydroxide or water-soluble alkaline earth metal salt, such as for example calcium chloride, to form soaps of the sulphonic acid present and the resulting soaps are then separated from the water and inorganic salts by the use of alcohol or other diluent or. by the use of a solvent for the soaps.
- sulphonic acids prepared as the above, and the soaps made therefrom will contain a small percentage of'manganese in chemical combination therewith. However, this is not to be regarded as due to the formation of manganese soaps with the sulphonic radicals present in the original acids. Rather, it is in general the result of the addition of manganese to the more reactive molecules at the point of oxidation.
- the purified sulphonic acids may be freed from the manganese by repeated extractions with an aqueous solution of a strong acid. However, the removal of the manganese is not necessary as its presence improves to an appreciable extent the stability of the alkaline earth'soaps made therefrom.
- Petroleum sulphonic acids which may be used advantageously to produce the purified alkaline earth sulphonates of this invention are preferably of the oil-soluble type which are obtained, for example, in the treatment of relatively heavy mineral oils, preferably so-called naphthenic oils such as California gas oils or lubricating oils, with concentrated or preferably fuming sulphuric acid.
- two types of sulphonic acids are produced, namely, so-called green sulphonic acids which are substantially oilinsoluble and mahogany acids which are oil-soluble
- mahogany acids are preferred, although the green acids may also yield certain oil-soluble soaps which are applicable to the purposes of the invention
- Other oil-soluble hydrocarbon sulphonic acids suitable for the'invention may be produced by the sulphonation of variou hydrocarbons provided the number of carbon atoms is sufllcient to render the resulting alkaline earth soaps soluble in the lubricating oil.
- alkaline earth sulphonates prepared as above, preferably without removing the combined manganese, are added to lubricating oils of suitable viscosity in the proportion of from 0.1% to 5%, the proportion of 1% to 5% being preferred.
- a very convenient method of preparing the oil of the desired percentage of soap is to prepare a stock solution of .oil containing more than 5% and preferably as much as 20% or more of soap and use this stock solution for making blends of any desired viscosity by blending the stock solution in proper amounts with oil of required viscosity.
- An alternate procedure of preparing oils according to the invention is to start with the crude sulphonic acids or sulphonate soaps dissolved in the desired lubricating oil.
- the oil containing the crude acids or soaps is then treated with acidified potassium permanganate. After agitation for a suflicient length of time the oil is freed from water and inorganic salts.
- the oil thus treated will contain purified sulphonic acids, any soap present having been decomposed by the mineral acid used.
- suflicient lime or other-alkaline earth hydroxide is added to combine with the sulphonic acids present. Excess lime is removed by settling, filtering, or centrifuging.
- the finished oil will have substantially all the desired properties of oil prepared by treating the acids separately with permanganate and adding soaps of the treated acids to the oil as described above.
- the base oil to which the purified alkaline earth sulphonates may be added may be of the .so-called parafiinic, naphthenic, or mixed-base tage, important in some applications, of having a somewhat higher viscosity-temperature coefficient.
- the sulphonic soaps of the present invention the corrosiveness of the parafiinic oils is reduced to a minimum, and it is possible to retain any advantage of low viscositytemperature coefficient inherent in parafiinic oils without the attendant corrosiveness ordinarily experienced.
- the alkaline earth sulphonates affect the viscosity of mineral oils but little when blended in proportions of 5% or less. Hence, the choice of the proper viscosity for the base oil depends upon the application intended for the finished oil. In the lubrication of the modern high speed Diesel engine oils having S. A. E. viscosity rating of 10, 20, and 30 are usually employed. For aircraft engines, oils of S. A; E. 40 and 50 and even higher are commonly used. However, due to the added oiliness imparted to the oil by the sulphonic soaps, greater ranges of viscosity are made Table I the soap is present in amount of 1.0% to 5.0%. 5.
- Q 6. A liquid lubricant for internal combustion Engmetype 3L g g B lg g engines comprising a body of petroleum lubricatengine. engine.
- a liquid lubricant for internal combustion engines comprising a body of petroleum lubri- Table II Calcium soap or 7 Calcium soap oi sulphonic acids Soap used No additive untreated sultreated in acphonic acids cordance with invention Engine type 0m V-8 gigord V-8 zgiord V-8.
- Viscosity of oil after, B. U. 210 F.
- a liquid lubrlcant'for internal combustionengines comprising a body of petroleum lubricateating oil containing dissolved alkaline earth metal soaps of the more stable constituents of petroleum sulphonic acids and alkaline earth metal soaps of the oxidation products of less stable constituents of petroleum sulphonic acids.
- a lubricant according to claim 8 in which the alkaline earth metal is calcium.
- a lubricant according to claim 8 in which the alkaline earth metal is calcium, and the soaps are present in an amount greater than 0.1%.
- a liquid lubricant for internal combustion engines comprising a body of petroleum lubricating oil containing dissolved alkaline earth metal soaps of organic acids oi the composition obtained by treating petroleum sulphonic acids with from 0.01 to 0.5 equivalent or potassium permanganate and retaining in the acids the organically combined manganese.
- a non-corrosive lubricating oil of superior non-sludging characteristics when employed under the conditions or high temperature and pressure met in internal combustion engines comprising a body of petroleum lubricating oil contain- 70 ing dissolved alkaline earth metal soaps oi the mote stable constituents of mahogany sulfonic acids-and alkaline earth metal soaps or the oxidation products or less stable constituents of mahogany sulfonic acids.
- the method or preparing a lubricating oil having superior antisludsine' and anticorrosion properties which comprises; treating sulphonic acids with sufllcient potassium permanganate to oxidize the more unstable components of said acids, separating the treated sulphonic acids irom inorganic material, forming alkaline earth metal soapsoi the resulting acids, and dissolving said soaps in a petroleum lubricating 011.
- the method of preparing a lubricating oil vhavingsuperior antisludging and anticorrosion properties which comprises: treating petroleum sulphonic acids with suflicient potassium per- 'manganate to oxidize the more unstable components of said acids, separating the treated sulphonic acids from inorganic material, forming alkaline earth metal soaps of the resulting acids, and dissolving said soaps in a petroleum lubrieating oil.
- method 01' preparing alubricating oil having superior antisludging. and anticorrosion properties which comprises: treating a lubricating oil containing dissolved sulphonic acids with an acidified aqueous solution of potassium permanganate in suillcient amount to oxidize the more unstable components or said acids, separating the resulting oil irom'the aqueous phase, and then converting the acids contained in the oil to their corresponding alkaline earth metal soap.
- the method of preparing a lubricating oil having superior antisludging and anticorrosion properties which comprises: treating sulphonic properties which comprises: treating sulphonic acids with suflicient potassium permanganate to oxidize the more unstable components 01 said acids, separating the treated sulphonic acids from inorganic material, extracting the thus treated sulphonic acids with a dilute strong mineral acid to remove combined manganese, forming alkaline earth metal soaps oi the resulting acids, and dissolving'said soaps in a petroleum lubricating'oil.
- treating sulphonic properties which comprises: treating sulphonic acids with suflicient potassium permanganate to oxidize the more unstable components 01 said acids, separating the treated sulphonic acids from inorganic material, extracting the thus treated sulphonic acids with a dilute strong mineral acid to remove combined manganese, forming alkaline earth metal soaps oi the resulting acids, and dissolving'said soaps in a petroleum lubric
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Jan. 16, 1945 COMPOUNDED OIL AND PROCESS OF PREPARING THE SAME Paul M. Ruedrich, Berkeley, Calif., assignor to Tide Water Associated Oil Company,- San Francisco, Calif., acorporation of Delaware No Drawing. Application January 9, 1943,
Serial No. 471,894
23 Claims.
This invention relates to improvements in lubricating oils and has for a principal object the provision of a lubricating oil having superior non-sludging characteristics when employed under the conditions of high temperature and pressure met in internal combustion engines.
Another object of the invention is to provide a lubricant which is non-corrosiveto the metal surfaces of an engine, especially to alloy bearmgs.
A further object is the purification of sulphonic acids and sulphonic soaps to render the same more suitable for use as additives to lubricating oils. Q
Other objects of the invention will be apparent in the following disclosure.
In the lubrication of high speed Diesel engines problems relative to adequate oiliness, carbon formation, prevention of ring-sticking, and wear are multitudinous. Modern aircraft engines offer similar problems to a great extent, although such problems are present at least to some extent in most internal combustion engines. solution of these problems it has become more or less common practice to incorporate metal soaps in the lubricating oil supplied to the crankcase of these engines. Among the soaps commonly employed alkaline earth sulphonates have been found particularly adapted to overcome.
most of the problems involved. However, these sulphonates, unless specially treated, cause undue corrosion to metal parts of the engine, es-
' pecially to bearings of the copper-lead alloy type. It is an object of this invention to produce al-- kaline earth sulphonates which, when added to lubricating oil in suitable amounts, will render the same highly resistant to such bearing corrosion and, to a great extent, free from ring-sticking, sludging, lacquer formation, and other unfailvorable characteristics common to lubricating o s.
In accordance with the invention it has been found that sulphonic acids derived from petroleum oils by treatment with concentrated sulphuric acid contain certain impurities which are the chief source of the corrosiveness generally experienced when their soaps are compounded with lubricating oils. If these impurities are removed or converted to non-corrosive compounds, the major portion'of the sulphonic acids produce alkaline earth soaps especially adapted for use in lubricating oils and oils blended with alkaline In the earth soaps of such purified sulphonic acids have vproven to be effective to a very high degree.
The liquid lubricant comprises a body of petroleum lubricating oil which contains dissolved alkaline earth metal soaps of the more stable constituents of petroleum sulfonic acids and alkaline earth metal soaps of the oxidation products of less stable constituents of petroleum sulfonic acids.
In the preparation and purification of the sulphonic acids, according to the invention, crude sulphonic acids derived from mineral oils are treated with potassium permanganate, preferably in an acidified aqueous solution, for a sumcient time to oxidize the more unstable compounds in the acids. For this purpose potassium permanganate in an amount equal'to approxi mately 0.01 to 0.5 equivalent weight per molecule of sulphonic acid is used, but in most cases best results are obtained when using from about, 0.1 to 0.2 equivalent weight. For example, since the equivalent weight of potassium permanganate is 31.6, a batch of 400 pounds of sulphonic acids having an average molecular weight of 400 (i. e., one pound-mole of sulphonic acids) may be treated with as little as 0.3 pound of potassium permanganate with noticeable effect, or the batch may be treated with as much as about 16 pounds of potassium permanganate without obtaining any considerable amount of deleterious reactions with the excess permanganate. Depending upon the nature of the sulphonic acids, best results usually will be obtained by treating such a batch of sulphonic acids with from about 3 to about 6 pounds of potassium permanganate. It is the purpose of the treatment, with permanganate to oxidize the more unstable components of the crude sulphonic acids and the exact quantity of permanganate for best results in each individual case may readily be determined by a skilled chemist by simple tests. For carrying out the treatment, an ordinary glazed or lead lined a itator equipped with means for mechanical or air agitation is suitable. However, various types of batch or continuous contacting apparatus may be used.
Although the reaction of the potassium permanganate with the unstable components may be. carried out; in various media, or even with dry permanganate by far the most satisfactory method is by contacting the sulphonic acids with the peracidified with a small amount of strong acid such as, for example, sulphuric acid. Care should be taken, of course, not to bring the permanganate into contact with concentrated strong acid, especially concentrated sulphuric acid, due to the danger of forming explosive mixtures. With efficient contacting the reaction of the potassium permanganate with the crude sulphonic acids takes place quite rapidly and, at ordinary temperatures, the reaction is nearly complete in several minutes. However, the reaction may be speeded up by applying a moderate degree of heat. For this purpose excellent results have been obtained using temperatures from 100 F. to 200 F., although temperatures somewhat higher or lower may be used. Also, in order to insure complete reaction it is well to continue the contacting for approximately one hour. After this treatment it will be found that the sulphonic acids are emulsified to a greater or less extent with the water present. They may be separated therefrom by the addition of some solvent such as alcohol or gasoline, the former uniting with the water of the emulsion and the latter uniting with the sulphonic acids. In either case two layers are formed, the non-aqueous layer containing the sulphonic acids. The sulphonic acids are then freed from any solvent and converted to calcium or other alkaline earth soaps by treatment withlime or with the hydroxide of magnesium, strontium, or barium, or in any other desired manner, such as for example, first forming the sodium soaps and converting these to the alkaline earth soaps by treatment with suitable alkaline earth metal salt. Alternately, the emulsion of purified sulphonic acids and water may be treated with lime or other alkaline earth metal hydroxide or water-soluble alkaline earth metal salt, such as for example calcium chloride, to form soaps of the sulphonic acid present and the resulting soaps are then separated from the water and inorganic salts by the use of alcohol or other diluent or. by the use of a solvent for the soaps.
Generally, it will be found that sulphonic acids prepared as the above, and the soaps made therefrom, will contain a small percentage of'manganese in chemical combination therewith. However, this is not to be regarded as due to the formation of manganese soaps with the sulphonic radicals present in the original acids. Rather, it is in general the result of the addition of manganese to the more reactive molecules at the point of oxidation. If desired, the purified sulphonic acids may be freed from the manganese by repeated extractions with an aqueous solution of a strong acid. However, the removal of the manganese is not necessary as its presence improves to an appreciable extent the stability of the alkaline earth'soaps made therefrom.
Petroleum sulphonic acids which may be used advantageously to produce the purified alkaline earth sulphonates of this invention are preferably of the oil-soluble type which are obtained, for example, in the treatment of relatively heavy mineral oils, preferably so-called naphthenic oils such as California gas oils or lubricating oils, with concentrated or preferably fuming sulphuric acid. In this kind of treatment two types of sulphonic acids are produced, namely, so-called green sulphonic acids which are substantially oilinsoluble and mahogany acids which are oil-soluble The mahogany acids are preferred, although the green acids may also yield certain oil-soluble soaps which are applicable to the purposes of the invention Other oil-soluble hydrocarbon sulphonic acids suitable for the'invention may be produced by the sulphonation of variou hydrocarbons provided the number of carbon atoms is sufllcient to render the resulting alkaline earth soaps soluble in the lubricating oil.
To form the oils of this invention alkaline earth sulphonates prepared as above, preferably without removing the combined manganese, are added to lubricating oils of suitable viscosity in the proportion of from 0.1% to 5%, the proportion of 1% to 5% being preferred. A very convenient method of preparing the oil of the desired percentage of soap is to prepare a stock solution of .oil containing more than 5% and preferably as much as 20% or more of soap and use this stock solution for making blends of any desired viscosity by blending the stock solution in proper amounts with oil of required viscosity.
An alternate procedure of preparing oils according to the invention is to start with the crude sulphonic acids or sulphonate soaps dissolved in the desired lubricating oil. The oil containing the crude acids or soaps is then treated with acidified potassium permanganate. After agitation for a suflicient length of time the oil is freed from water and inorganic salts. The oil thus treated will contain purified sulphonic acids, any soap present having been decomposed by the mineral acid used. After separation of the acid and excess permanganate, suflicient lime or other-alkaline earth hydroxide is added to combine with the sulphonic acids present. Excess lime is removed by settling, filtering, or centrifuging. The finished oil will have substantially all the desired properties of oil prepared by treating the acids separately with permanganate and adding soaps of the treated acids to the oil as described above.
The base oil to which the purified alkaline earth sulphonates may be added may be of the .so-called parafiinic, naphthenic, or mixed-base tage, important in some applications, of having a somewhat higher viscosity-temperature coefficient. By the use of the sulphonic soaps of the present invention the corrosiveness of the parafiinic oils is reduced to a minimum, and it is possible to retain any advantage of low viscositytemperature coefficient inherent in parafiinic oils without the attendant corrosiveness ordinarily experienced.
The alkaline earth sulphonates affect the viscosity of mineral oils but little when blended in proportions of 5% or less. Hence, the choice of the proper viscosity for the base oil depends upon the application intended for the finished oil. In the lubrication of the modern high speed Diesel engine oils having S. A. E. viscosity rating of 10, 20, and 30 are usually employed. For aircraft engines, oils of S. A; E. 40 and 50 and even higher are commonly used. However, due to the added oiliness imparted to the oil by the sulphonic soaps, greater ranges of viscosity are made Table I the soap is present in amount of 1.0% to 5.0%. 5. A lubricant according to claim 1 in which 031mm g of the soap is present in amount in excess of 5%, son 12:33 5 2 igg g g ggigf thus making the lubricant suitable for use as a p phonic wa with the 5 stock solution to be later diluted with additional Invention petroleum oil. Q 6. A liquid lubricant for internal combustion Engmetype 3L g g B lg g engines comprising a body of petroleum lubricatengine. engine. ing oil containing dissolved alkaline earth metal 'ggg fi-g 10 soaps of petroleum sulphonic acids, the normally Hours ,run m i more unstable components of said acids having para no, 138310011 naphthemm" mphthemc been oxidized and retained in the lubricant in %A.E%grade go go oxldlzed form.
er cen soap r Appearance oipiston Covered%with 100% clean after A l quid lubricant for internal combustion hard, black wiping. in engines comprising a body of petroleum lubricatac Hen Ring grooves Deep aymmgrd very little so" me Oll containing dissolved alkaline earth metal carbon behind carbon. soaps of mahogany sulphonic acids, the normally llnll'S.
Piston liner .Q Free from abra- Free from abramore mlsliable componepts sald aclds having sons. sions. been oxidized and retained in the lubricant in Oil filter Fairlyt heavlydde- N0 sludge. no oxidized form 1 posi 0 sn ge. Cu-Pb bearings, loss, mgs. 291... 64. 8. A liquid lubricant for internal combustion engines comprising a body of petroleum lubri- Table II Calcium soap or 7 Calcium soap oi sulphonic acids Soap used No additive untreated sultreated in acphonic acids cordance with invention Engine type 0m V-8 gigord V-8 zgiord V-8.
2,566IIIIIIIIIIII 2,500. so 5o 50. v
50% paraflinlc.-. 50% parafilnicm 50% parafllnic.
%% naphthenic. gg% naphthenic 33% naphthenic.
Percent soap crankcase temp., "F.
Oil change Cleanliness oi pistons Carbon deposits top of pistons, gms
Carbon deposits, bottom oi pistonsfi ms.
Viscosity of oil, before, S. U. 210
Viscosity of oil, after, B. U. 210 F.
Acidity of oil. before KOH/gm Acidity of oil, alter, lIOH/gm The above tabulations illustratethe freedom from bearing-corrosion obtained by oils prepared in accordance with the invention. Also, they demonstrate the superior properties with respect to freedom from sludging, carbon-formation, and ring-sticking.
An additional efiect noticeable in engines using fuels compounded with tetraethyl lead is the absence of lead-salt deposits customarily round in the crankcase and on the underside of the pistons wherethis type of fuel is used. Such deposits are at times particularly troublesome due to the abrasive action of the salts on the moving surfaces of the engine. Oils compounds with metallic soaps not prepared in accordance with the present invention have proven ineflective in preventing these deposits. It is, therefore, an ob- Ject of the invention to produce a lubricating oil which will effectively restrain the formation of lead-salt deposits in the crankcases of engines using leaded fuels.
I claim: Y
1. A liquid lubrlcant'for internal combustionengines comprising a body of petroleum lubricateating oil containing dissolved alkaline earth metal soaps of the more stable constituents of petroleum sulphonic acids and alkaline earth metal soaps of the oxidation products of less stable constituents of petroleum sulphonic acids.
9. A lubricant according to claim 8, in which the alkaline earth metal is calcium.
10. A lubricant according to claim 8, in which the alkaline earth metal is calcium, and the soaps are present in an amount greater than 0.1%.
11. A lubricant according to claim 8 in which the soap contains'a small percentage of manganese in chemical combination therewith.
12. A liquid lubricant for internal combustion engines comprising a body of petroleum lubricating oil containing dissolved alkaline earth metal soaps of organic acids oi the composition obtained by treating petroleum sulphonic acids with from 0.01 to 0.5 equivalent or potassium permanganate and retaining in the acids the organically combined manganese.
13. A non-corrosive lubricating oil of superior non-sludging characteristics when employed under the conditions or high temperature and pressure met in internal combustion engines comprising a body of petroleum lubricating oil contain- 70 ing dissolved alkaline earth metal soaps oi the mote stable constituents of mahogany sulfonic acids-and alkaline earth metal soaps or the oxidation products or less stable constituents of mahogany sulfonic acids.
14. The method or preparing a lubricating oil having superior antisludsine' and anticorrosion properties which comprises; treating sulphonic acids with sufllcient potassium permanganate to oxidize the more unstable components of said acids, separating the treated sulphonic acids irom inorganic material, forming alkaline earth metal soapsoi the resulting acids, and dissolving said soaps in a petroleum lubricating 011.
15. The method of claim 14 in which the amount of potassium permanganate used is be- 7 tween 0.01 and 0.5 equivalent per molecule of sulphonic acid treated.
16. The method of claim 14 in which the amount or potassium permanganate used is be: tween about 9.1 and about 0.2 equivalent per molecule of sulphonic acid treated.
1'7. The method claim, 14 in which the alkaline'earth metal is calcium.
' 18. The method of preparing a lubricating oil vhavingsuperior antisludging and anticorrosion properties which comprises: treating petroleum sulphonic acids with suflicient potassium per- 'manganate to oxidize the more unstable components of said acids, separating the treated sulphonic acids from inorganic material, forming alkaline earth metal soaps of the resulting acids, and dissolving said soaps in a petroleum lubrieating oil.
19.- The method oi! preparing a lubricating oil having superior antisludging and anticorrosion acids with sumcient potassium permanganate in an acidified aqueous solution to oxidize the more unstable components of said aclds,.separating the treated sulphonic acids from the aqueous phase, forming alkaline earth metal soaps of the resultingacids, and dissolving said soaps in a petroleum lubricating 011.
. method 01' preparing alubricating oil having superior antisludging. and anticorrosion properties which comprises: treating a lubricating oil containing dissolved sulphonic acids with an acidified aqueous solution of potassium permanganate in suillcient amount to oxidize the more unstable components or said acids, separating the resulting oil irom'the aqueous phase, and then converting the acids contained in the oil to their corresponding alkaline earth metal soap.
21. The method of preparing a lubricating oil having superior antisludging and anticorrosion properties which comprises: treating sulphonic properties which comprises: treating sulphonic acids with suflicient potassium permanganate to oxidize the more unstable components 01 said acids, separating the treated sulphonic acids from inorganic material, extracting the thus treated sulphonic acids with a dilute strong mineral acid to remove combined manganese, forming alkaline earth metal soaps oi the resulting acids, and dissolving'said soaps in a petroleum lubricating'oil.
22. In a process wherein sulphonic acids are partially oxidized to improve their stability and the thus treated acids are converted into alkaline earth metal soaps which are dissolved in a petroleum lubricating oil, the combination oi,
PAUL M. nonunion.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US471894A US2367435A (en) | 1943-01-09 | 1943-01-09 | Compounded oil and process of preparing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US471894A US2367435A (en) | 1943-01-09 | 1943-01-09 | Compounded oil and process of preparing the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2367435A true US2367435A (en) | 1945-01-16 |
Family
ID=23873408
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US471894A Expired - Lifetime US2367435A (en) | 1943-01-09 | 1943-01-09 | Compounded oil and process of preparing the same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2367435A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2454826A (en) * | 1948-11-30 | Viscosity reduction of petroleum | ||
| US2673183A (en) * | 1949-08-16 | 1954-03-23 | Standard Oil Co | Metal cutting oil derived from oxidized petroleum oil |
| US3048607A (en) * | 1958-12-22 | 1962-08-07 | Gulf Research Development Co | Oil soluble amine salts of long chain alpha-sulfocarboxylic acids |
| US3388062A (en) * | 1967-01-27 | 1968-06-11 | Lockheed Aircraft Corp | Cutting fluids for machining and/or working of titanium and its alloys |
-
1943
- 1943-01-09 US US471894A patent/US2367435A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2454826A (en) * | 1948-11-30 | Viscosity reduction of petroleum | ||
| US2673183A (en) * | 1949-08-16 | 1954-03-23 | Standard Oil Co | Metal cutting oil derived from oxidized petroleum oil |
| US3048607A (en) * | 1958-12-22 | 1962-08-07 | Gulf Research Development Co | Oil soluble amine salts of long chain alpha-sulfocarboxylic acids |
| US3388062A (en) * | 1967-01-27 | 1968-06-11 | Lockheed Aircraft Corp | Cutting fluids for machining and/or working of titanium and its alloys |
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