US2443585A - Cylinder oils - Google Patents
Cylinder oils Download PDFInfo
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- US2443585A US2443585A US687536A US68753646A US2443585A US 2443585 A US2443585 A US 2443585A US 687536 A US687536 A US 687536A US 68753646 A US68753646 A US 68753646A US 2443585 A US2443585 A US 2443585A
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- steam
- cylinder
- oil
- acid
- per cent
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- 239000010727 cylinder oil Substances 0.000 title description 18
- 239000007795 chemical reaction product Substances 0.000 description 21
- 239000002253 acid Substances 0.000 description 20
- 150000002148 esters Chemical class 0.000 description 20
- 239000003921 oil Substances 0.000 description 19
- 239000000654 additive Substances 0.000 description 18
- 239000000047 product Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 239000002480 mineral oil Substances 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 238000003892 spreading Methods 0.000 description 13
- 230000007480 spreading Effects 0.000 description 13
- 235000010446 mineral oil Nutrition 0.000 description 12
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 11
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 11
- 125000001931 aliphatic group Chemical group 0.000 description 10
- 238000005461 lubrication Methods 0.000 description 10
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 9
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 9
- 239000001630 malic acid Substances 0.000 description 9
- 235000011090 malic acid Nutrition 0.000 description 9
- 238000006386 neutralization reaction Methods 0.000 description 9
- 230000000996 additive effect Effects 0.000 description 8
- 229940055577 oleyl alcohol Drugs 0.000 description 8
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 238000009833 condensation Methods 0.000 description 7
- 230000005494 condensation Effects 0.000 description 7
- 150000001261 hydroxy acids Chemical class 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 230000001050 lubricating effect Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
- 239000007859 condensation product Substances 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- -1 fatty acid esters Chemical class 0.000 description 5
- 229940049920 malate Drugs 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000010699 lard oil Substances 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 235000021588 free fatty acids Nutrition 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241000120283 Allotinus major Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010697 neat foot oil Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000004551 spreading oil Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 235000011044 succinic acid Nutrition 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000003760 tallow Substances 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic 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
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/288—Partial esters containing free carboxyl groups
-
- 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
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/135—Steam engines or turbines
Definitions
- the present invention relates to the lubrication of steam cylinders and, more particularly, to improved steam cylinderoils containing a minor proportion of a material increasing the spreading characteristics of steam cylinder mineral oils.
- the problem of lubricating steam cylinders involves at least one factor that is not encountered in the usual problems of lubricating surfaces which move relative to each other.
- the presence of a relatively large amount of Water and high temperatures is not encountered. Consequently, many of the additives now incorporated in lubricants for internal combustion engines are not suitable for use in the lubrication of steam cylinders.
- the role of the additive appears to be that of assisting in the spreading of the oil over the internal surface of the steam cylinder at the temperatures and pressures existing in the cylinder of a steam engine. Less mineral oil is required to provide satisfactory lubrication when the oil is spread uniformly over the internal surface of the cylinder. On the other hand, when the oil collects in globules larger amounts of oil are required to provide satisfactory lubrication of a steam cylinder.
- the use of a small amount of oil to properly lubricate a steam cylinder is acuned by two advantages, (1) lower lubrication cost, and (2) less carbon deposited on the cylinder Walls. 7
- the present invention comprises mixing about 0.1 per cent to about 1 per cent by weight of the product produced by condensing an aliphatic hydroxy dicanb'oxylic acid with a monohydric alcohol having at least five carbon atoms with a mineral oil fraction, known to the art as steam cylinder stock, and having a Saybolt Viscosity at 210 degrees Fahrenheit of about 100 seconds to about 300 seconds and a minimum flash point of about 425 degrees Fahrenheit.
- the additive is the reaction product of an aliphatic dicarboxylic hydroxy acid and an unsaturated aliphatic monohydric alcohol. Of these latter compounds, the reaction product of oleyl alcohol and malic acid is especially preferred.
- Products produced by the reaction of a given amount of hydroxy aliphatic dicarboxylic acid and the s-toichiometric amount of monohydric aliphatic alcohol necessary to produce either the neutral ester or the acid ester have given satisfactory results.
- the measure of the efficacy of an additive in a steam cylinder oil is the efiect of the additive on the rate and degree of spreading of a drop or globule of oil on the surface of Water.
- reaction products of oleyl alcohol, lauryl alcohol and stearyl alcohol with malic acid, tartaric acid, succinic acid and maleic acid were selected as illustrative of the effect of various condensation products upon the lubricating effect of a steam cylinder stock selected as the base steam cylinder stock and having the properties set forth hereinafter:
- Flash point 500 F. (minimum) S. U. V. at 100 211 seconds 'Saponification number, 190
- Reaction product A was obtained by reacting 0.25 mole of malic acid and an amount of commercial lauryl alcohol slightly in excess of 0.5 mole without a catalyst.
- the reactionmixture was digested at about 240 to about 250 degrees Fahrenheit for about 3 hours. Thereafter about 40 par-ts by volume of toluene were added and the mixture refluxed for about 6 hours at a pot temperature of about 285 to about 290 degrees Fahrenheit.
- the reaction mixture was then topped under vacuum.
- the residue comprising the reaction product immediately after preparation had a neutralization number (N. N.) of 16 which is equivalent to a concentration of about 10 per cent of the acid ester.
- Reaction product B was obtained by reacting about 0.2 mole of malic acid and an amount of commercial stearyl alcohol sold under the trade name of Stenol slightly in excess of about-0.4 mole in the absence of a catalyst.
- Stenol is a mixture of C18 alcohols containing substantially no unsaturated alcohols.
- the reaction mixture was digested at 240: 10 degrees Fahrenheit (bath temperature about 250 to about 260 degrees Fahrenheit) for about 4 hours under atmospheric pressure. Thereafter the mixture was digested un-.- der a vacuum for about 11 hours at a temperature of about 250 to about 260 degrees Fahrenheit.
- the reaction product immediately after preparation had a neutralization number (N. N.) of 26.
- vReaction products C and G were obtained by reacting 1 mole of malic acid and an amount of commercial oleyl alcohol (sold under the trade name of Ocenol) slightly in excess of 2 moles in the absence of catalyst.
- the reaction mixture was digested for several hours and the reaction product treated to separate acid esters from neutral esters.
- the reaction mixture immediately after preparation had a neutralization number (N. N.) of 17.
- the reaction mixture was extracted to remove Water soluble acids.
- a petroleum ether solution of the residue was extracted with 2 per cent solution of potassium hydroxide in 50 per cent alcohol to remove the acid esters.
- the residue from the alcoholic potassium hydroxide solution is neutral ester (product C).
- the alcoholic potassium hydroxide solution of acid ester was acidified and the acid ester recovered (product G)
- the neutralization number (N. N.) of product G immediately after preparation was 106, equivalent to about 70 per cent acid ester.
- Product F was prepared by digesting about 0.33 mole of maleic acid and an amount of Ocenol slightly in excess of 0.66 mole for about 0.75 hour. Thereafter about 50 to about 60 parts by volume of toluene were added and the mixture refluxed at a pot temperature of about 285 degrees Fahrenheit for about hours. The reaction mixture was filtered and topped.
- Product D was prepared by mixing about 1 mole of Ocenol, about 0.5 mole of succinic anhydride and about 350 cubic centimeters of xylene. The mixture was heated to reflux and maintained at about reflux temperature for about 12 hours. Water produced in the reaction was removed while refluxing. The reaction mixture was filtered and the filtrate topped to remove the xylene. The topped filtrate had a neutralization value of 19.0.
- Product E was produced from tartaric acid and oleyl alcohol in a manner similar to the foregoing procedures.
- the product had a neutralization value of about 7 immediately after prepara- 8, 12 and 13). It will also be observed that there is no apparent correlation between surface tension and the rate and degree of spreading of an oil.
- steam cylinder oil per se has a surface tension of 33 dynes per centimeter 1. cm.) at 7'7 degrees Fahrenheit but forms a globule on the surface of clean Water at 190 degrees Fahrenheit.
- the same steam cylinder oil containin 0.67 per cent of mono-oleyl malate has a surface tension of 32 dynes per centimeter but spreads instantaneously and completely (compare items 2 and 13).
- reaction products of an aliphatic monohydric alcohol having at least 5 carbon atoms and aliphatic dicarboxylic hydroxy acid, which reaction products have a neutralization number of at least 5 are effective additives for lubricating oils to be used in the lubrication of steam cylinders.
- an effective steam cylinder lubricant has an interfacial tension with distilled water at 77 degrees Fahrenheit not greater than about 25 dynes per centimeter and preferably has an interfacial tension of about 20 or less.
- a steam cylinder lubricant consisting essentially of a mineral oil fraction having a Sayb0lt viscosity from about 100 seconds to about 300 seconds, at 210 F., and a flash point of at least about 425 F., and about 0.2 per cent of the esterification reaction product of oleyl alcohol and malic acid, said reaction product containing about 67 per cent of an acid ester of said alcohol and said acid.
- a steam cylinder lubricant consisting essentially of a mineral oil fraction having a Saybolt viscosity from about 100 seconds to about 300 seconds at 210 F., and a flash point of at least about 425 F., and from about 0.2 per cent tion and an OH value oi 179 average. to about 1 per cent of the esterification reactlon Per cent Per cent Inter- Formula N Acid Acid suffice facial Spreading Characteristics No. Formulation fg i g Ester in Ester in gggfi gp Tension 190 F.
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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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
Description
Patented June 15, 1948 warn-:1) STATE CYLINDER OILS Leon Salz, Brooklyn, and Samuel P. Marley, Bayside, N. Y., assignors to Socony-Vacuum Oil Company, Incorporated, acorporation of New York No Drawing. Application July 31, 1946, Serial No. 687,536
2 Claims.
The present invention relates to the lubrication of steam cylinders and, more particularly, to improved steam cylinderoils containing a minor proportion of a material increasing the spreading characteristics of steam cylinder mineral oils.
The operation of steam engines involves lubrication of the cylinder walls in such a manner as to reduce the friction and wear of the piston and the walls. When conditions within the cylinder are such that substantially no condensation occurs within the cylinder, little-difficulty is experienced in lubricating the cylinder with pure mineral oil. However, the ideal conditions under which no condensation occurs within the cylinder are rarely achieved in industrial operations. Condensation is eliminated only when the steam is superheated to such a degree that the expansion occurring in the cylinder is insuflicient to lower the temperature of steam to that at which condensation occurs or when the steam is substantially dry throughout the piston cycle. Consequently, the steam in the cylinder is generally wet. The art has recognized that condensation practically always occurs in the cylinders of steam engines and has for many years striven to provide compounded oils which will lubricate the cylinder satisfactorily in the presence of condensate.
The art has recognized that when straight mineral oil is used under wet steam conditions, i, e., when condensate forms in the cylinder, the adhesion of the oil to the cylinder walls is poor and the quantity of oil required for satisfactory lubrication becomes excessive. This, in turn, causes the formation of carbon deposits which interfere with the smooth operation of the engine,
In order to improve the adhesion and spread ing of pure mineral oils to cylinder walls under the usually prevailing wet steam conditions, various additives have been blended with cylinder stocks. In the past the conventional additives have been fatty acid esters of glycerol or other alcohols such as lard, tallow, neatsfoot oil and degras. These additives under the conditions existing in the steam cylinder, i. e., in the presence of water and at high temperature and pressures, are hydrolyzed to the free fatty acids and the alcohol.
At the present time it is general practice to mix with the base mineral oil cylinder stock up to 12 per cent by weight of the afore-enumerated additives depending upon the quality of the steam in the cylinder. When the steam is superheated or dry throughout the piston cycle, compounding, i. e. mixing mineral oil and additive, is neither necessary nor desirable. However, as the quality of the steam decreases, i. e., as the amount of the liquid phase in the steam increases, it is necessary to increase the amount of additive. In other words, the wetter the steam, the greater the amount of additive. Accordingly, it would appear that the problem of lubricating steam cylinders involves spreading oil over a surface which is covered with a layer of water. In other words, the problem of lubricating steam cylinders involves at least one factor that is not encountered in the usual problems of lubricating surfaces which move relative to each other. For example, in lubricating the cylinder walls of internal combustion engines, the presence of a relatively large amount of Water and high temperatures is not encountered. Consequently, many of the additives now incorporated in lubricants for internal combustion engines are not suitable for use in the lubrication of steam cylinders.
The role of the additive appears to be that of assisting in the spreading of the oil over the internal surface of the steam cylinder at the temperatures and pressures existing in the cylinder of a steam engine. Less mineral oil is required to provide satisfactory lubrication when the oil is spread uniformly over the internal surface of the cylinder. On the other hand, when the oil collects in globules larger amounts of oil are required to provide satisfactory lubrication of a steam cylinder. The use of a small amount of oil to properly lubricate a steam cylinder is ac companied by two advantages, (1) lower lubrication cost, and (2) less carbon deposited on the cylinder Walls. 7
It has now been found that the disadvantages of prior art steam cylinder oils can be overcome by adding a minor proportion of the condensation product of a dicarboxylic hydroxy acid with a monohydric alcohol and preferably the reaction product of an unsaturated monohydric alcohol having about 16 to about 20 carbon atoms in the molecule and a dicarboxylic aliphatic hydroxy acid to a mineral oil fraction meeting the specifications for steam cylinders oils.
It is an object of the present invention to provide a compound cylinder oil containing a minor proportion of the condensation product of an aliphatic dicarboxylic hydroxy acid and a monohydric alcohol. It is another object of the present invention to provide a compound cylinder oil having an interfacial tension at 77 degrees Fahrenheit with distilled water of not more than about 25 dynes per centimeter and comprising a. major proportion of steam cylinder oil fraction of a mineral oil and a minor proportion of the condensation product of an aliphatic dicarboxylic hydroxy acid and a monohydric alcohol.
It is a further object of the present invention to provide a steam cylinderoil having an interfacial tension at '77 de rees Fahrenheit with distilled water of not more than about 25 dynes per centimeter and comprising a major proportion of a mineral oil fraction having a Saybolt viscosity at 210 degrees Fahrenheit of about seconds to about 300 seconds and a minimum flash point of about 425 degrees Fahrenheit and a minor proportion of a condensation product of an aliphatic dicarboxylic hydroxy acid and an unsaturated monohydric alcohol. Other objects and advantages will become apparent from the following description.
The present invention, generally stated, comprises mixing about 0.1 per cent to about 1 per cent by weight of the product produced by condensing an aliphatic hydroxy dicanb'oxylic acid with a monohydric alcohol having at least five carbon atoms with a mineral oil fraction, known to the art as steam cylinder stock, and having a Saybolt Viscosity at 210 degrees Fahrenheit of about 100 seconds to about 300 seconds and a minimum flash point of about 425 degrees Fahrenheit. Preferably, the additive is the reaction product of an aliphatic dicarboxylic hydroxy acid and an unsaturated aliphatic monohydric alcohol. Of these latter compounds, the reaction product of oleyl alcohol and malic acid is especially preferred.
Products produced by the reaction of a given amount of hydroxy aliphatic dicarboxylic acid and the s-toichiometric amount of monohydric aliphatic alcohol necessary to produce either the neutral ester or the acid ester have given satisfactory results. These products have a neutralization number within the range of 5 milligrams to 100 milligrams KOH per gram which, e. g., when calculated in terms of the acid ester of oleyl malate coon n- -n n-(t-on OOOCisHan Acid ester of oleyl malate (molecular weight=384) is equal to about 3.5 per cent to about 69 per cent mono-oleyl malate. However, products having acid ester concentration up to 100 per cent may be used. It is preferred to use products of the condensation of oleyl alcohol and malic acid which have a neutralization number of about 9 to about 100 milligrams of KOH per gram equivalent to an acid ester concentration calculatedas mono-oleyl malate of about 6 to about 69 per cent.
As has been pointed out hereinbefore, the measure of the efficacy of an additive in a steam cylinder oil is the efiect of the additive on the rate and degree of spreading of a drop or globule of oil on the surface of Water. The data present: ed in the following table shows Very well that typical products produced by the condensation of an aliphatic monohydric alcohol and an aliphatic dicarboxylic hydroxy acid increase the tendency of a steam cylinder oil to spread on the surface of water. The reaction products of oleyl alcohol, lauryl alcohol and stearyl alcohol with malic acid, tartaric acid, succinic acid and maleic acid were selected as illustrative of the effect of various condensation products upon the lubricating effect of a steam cylinder stock selected as the base steam cylinder stock and having the properties set forth hereinafter:
Steam cylinder stock A. P. I. gravity, 24.8
Flash point, 610 F.
S. U. V. at 210 F., 235 seconds Carbon residue, 2.8% (maximum) To provide a means of comparison with prior art additives, lard oil was selected a representative. The lard oil had the properties set forth hereinafter:
Specific gravity, 0.916
Flash point, 500 F. (minimum) S. U. V. at 100 211 seconds 'Saponification number, 190
mum) Iodine number, 75 (maximum) Free fatty acids, 3% (maximum) .Comparison'of the efiect of the addition agents disclosed herein upon the lubrication of steam cylinders has been correlated with the rate of spreading and completeness of spreading of cylinder oil and compounded cylinder oil, with surface tension and with interfacial tension. Those oils which provide satisfactory cylinder lubrication are characterized by almost instantaneous and complete spreading in the test described hereinafter and by an interfacial tension with dis: tilled water of notmore than about 25 dynes per centimeter (d. cm.) at '77 degrees Fahrenheit. The spreading characteristics of mineral oil and (minimineral oil compounded with various prior art and novel additives have been compared by ale lowing a drop of test oil weighingapproximately 35 milligrams to fall from the orifice of 5 millimeter glass tubing onto the surface of a pool of I distilled water at a temperature of about 190 degrees Fahrenheit held in a Petri dish cover having a diameter of 10 centimeters. The container was cleaned before each test by washing with water, drying with a soft towel, washing again in a bath of petroleum ether and a bath of acetone and drying. The surface and interfacial tensions of the various oils were determined with a du Nouy Tensiometer. Data thus obtained are tabulated in the table for the test steam cylinder oil and the oil compounded with prior art additives, the novel additives and analogous esters.
Reaction product A was obtained by reacting 0.25 mole of malic acid and an amount of commercial lauryl alcohol slightly in excess of 0.5 mole without a catalyst. The reactionmixture was digested at about 240 to about 250 degrees Fahrenheit for about 3 hours. Thereafter about 40 par-ts by volume of toluene were added and the mixture refluxed for about 6 hours at a pot temperature of about 285 to about 290 degrees Fahrenheit. The reaction mixture was then topped under vacuum. The residue comprising the reaction product immediately after preparation had a neutralization number (N. N.) of 16 which is equivalent to a concentration of about 10 per cent of the acid ester.
Reaction product B was obtained by reacting about 0.2 mole of malic acid and an amount of commercial stearyl alcohol sold under the trade name of Stenol slightly in excess of about-0.4 mole in the absence of a catalyst. -(As those skilled in the art know, Stenol is a mixture of C18 alcohols containing substantially no unsaturated alcohols.) The reaction mixture was digested at 240: 10 degrees Fahrenheit (bath temperature about 250 to about 260 degrees Fahrenheit) for about 4 hours under atmospheric pressure. Thereafter the mixture was digested un-.- der a vacuum for about 11 hours at a temperature of about 250 to about 260 degrees Fahrenheit. The reaction product immediately after preparation had a neutralization number (N. N.) of 26.
vReaction products C and G were obtained by reacting 1 mole of malic acid and an amount of commercial oleyl alcohol (sold under the trade name of Ocenol) slightly in excess of 2 moles in the absence of catalyst. The reaction mixture was digested for several hours and the reaction product treated to separate acid esters from neutral esters. The reaction mixture immediately after preparation had a neutralization number (N. N.) of 17. The reaction mixture was extracted to remove Water soluble acids. A petroleum ether solution of the residue was extracted with 2 per cent solution of potassium hydroxide in 50 per cent alcohol to remove the acid esters. The residue from the alcoholic potassium hydroxide solution is neutral ester (product C). The alcoholic potassium hydroxide solution of acid ester was acidified and the acid ester recovered (product G) The neutralization number (N. N.) of product G immediately after preparation was 106, equivalent to about 70 per cent acid ester.
Product F was prepared by digesting about 0.33 mole of maleic acid and an amount of Ocenol slightly in excess of 0.66 mole for about 0.75 hour. Thereafter about 50 to about 60 parts by volume of toluene were added and the mixture refluxed at a pot temperature of about 285 degrees Fahrenheit for about hours. The reaction mixture was filtered and topped.
Product D was prepared by mixing about 1 mole of Ocenol, about 0.5 mole of succinic anhydride and about 350 cubic centimeters of xylene. The mixture was heated to reflux and maintained at about reflux temperature for about 12 hours. Water produced in the reaction was removed while refluxing. The reaction mixture was filtered and the filtrate topped to remove the xylene. The topped filtrate had a neutralization value of 19.0.
Product E was produced from tartaric acid and oleyl alcohol in a manner similar to the foregoing procedures. The product had a neutralization value of about 7 immediately after prepara- 8, 12 and 13). It will also be observed that there is no apparent correlation between surface tension and the rate and degree of spreading of an oil. Thus, steam cylinder oil per se has a surface tension of 33 dynes per centimeter 1. cm.) at 7'7 degrees Fahrenheit but forms a globule on the surface of clean Water at 190 degrees Fahrenheit. On the other hand, the same steam cylinder oil containin 0.67 per cent of mono-oleyl malate has a surface tension of 32 dynes per centimeter but spreads instantaneously and completely (compare items 2 and 13). Accordingly, it is manifest that reaction products of an aliphatic monohydric alcohol having at least 5 carbon atoms and aliphatic dicarboxylic hydroxy acid, which reaction products have a neutralization number of at least 5 are effective additives for lubricating oils to be used in the lubrication of steam cylinders. It will also be observed that an effective steam cylinder lubricant has an interfacial tension with distilled water at 77 degrees Fahrenheit not greater than about 25 dynes per centimeter and preferably has an interfacial tension of about 20 or less.
We claim:
1. A steam cylinder lubricant consisting essentially of a mineral oil fraction having a Sayb0lt viscosity from about 100 seconds to about 300 seconds, at 210 F., and a flash point of at least about 425 F., and about 0.2 per cent of the esterification reaction product of oleyl alcohol and malic acid, said reaction product containing about 67 per cent of an acid ester of said alcohol and said acid.
2. A steam cylinder lubricant consisting essentially of a mineral oil fraction having a Saybolt viscosity from about 100 seconds to about 300 seconds at 210 F., and a flash point of at least about 425 F., and from about 0.2 per cent tion and an OH value oi 179 average. to about 1 per cent of the esterification reactlon Per cent Per cent Inter- Formula N Acid Acid suffice facial Spreading Characteristics No. Formulation fg i g Ester in Ester in gggfi gp Tension 190 F.
Additive Formula 77 F.
Distilled water 70 Steam cylinder oil 33 39 Globule; no spreading. 99% S. O. 0., 1% Lard oil 4.1 32 31 Globule; gradually widening to partial 1 spreading. 97% S. O. 0., 3% Lard oil 4. 1 32 22 Instantaneous and complete. 93% S. O. 0., 7% Lard O11 4. 1 32 16 Instantaneous and complete. 99% S. C. O., 1% Reaction Product A. 11. 3 6 0. 06 32 13 Do. 99% S. C. 0., 1% Reaction Product B. 12.8 9 0. 09 32 25 Do. 99% S. O. 0., 1% Reaction Product 0. 12.5 8 0. 08 32 11 Do. 99% S. O. 0., 1% Reaction Product D- 8. 7 6 0. 06 32 29 Gradual; only partial. 99% S. C. 0., 1% Reaction Product E. 9. 2 6 0. 06 32 10 Instantaneous and complete. 99% S. C. 0., 1% Reaction Product F. 15. 6 10 0. 10 32 33 Gradual; only partial. 99.87g (8} C. 0., 0.2% Reaction Prod- 98. 0 67 0.13 32 14 Instantaneous and complete. uc 99% S. C. 0., 1% Reaction Product G. 98.0 67 0. 67 32 6 Do. 99.8% S. O. 0., 0.2% oleyl alcohol. 0.14 33 36 Gradual; only partial. 99.8% S. C. 0., 0.2% Malic acid..... Insoluble 1n Steam cylinder oil 1 Values in dynes per centimeter.
1 The term partial signifies that the oil film occupiedcver V but less than the entire surface of the Petri dish. 3 The term complete signifies that the oil film occupied the entire surface of the Petri dish.
be noted that an increase in the concentration of acid ester in the steam cylinder oil beyond about 0.10 per cent while producing a decrease in interfacial tension appears to provide diminishing returns in so far as rate and completeness of spreading is concerned (compare items product of oleyl alcohol and malic acid, said reaction product containing about 67 per cent of an acid ester of said alcohol and said acid.
LEON SALZ. SAMUEL P. MARLEY.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,370,299 Farrington Feb. 27, 1945 2,096,390 Burwell Oct. 19, 1937 2,025,984 Harris Dec. 31, 1935
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US687536A US2443585A (en) | 1946-07-31 | 1946-07-31 | Cylinder oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US687536A US2443585A (en) | 1946-07-31 | 1946-07-31 | Cylinder oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2443585A true US2443585A (en) | 1948-06-15 |
Family
ID=24760799
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US687536A Expired - Lifetime US2443585A (en) | 1946-07-31 | 1946-07-31 | Cylinder oils |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2443585A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2493483A (en) * | 1948-04-26 | 1950-01-03 | Shell Dev | Marine engine lubricant |
| US2810744A (en) * | 1955-03-25 | 1957-10-22 | Exxon Research Engineering Co | Polymerization process for preparing lubricant additives and products |
| US3219657A (en) * | 1961-02-27 | 1965-11-23 | Monsanto Co | Saccharide polydicarboxylate half-esters |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2025984A (en) * | 1934-01-08 | 1935-12-31 | Benjamin R Harris | Ester of hydroxy carboxylic acids |
| US2096390A (en) * | 1934-12-27 | 1937-10-19 | Alox Corp | Compounded lubricants |
| US2370299A (en) * | 1941-02-26 | 1945-02-27 | Standard Oil Co California | Compounded lubricant |
-
1946
- 1946-07-31 US US687536A patent/US2443585A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2025984A (en) * | 1934-01-08 | 1935-12-31 | Benjamin R Harris | Ester of hydroxy carboxylic acids |
| US2096390A (en) * | 1934-12-27 | 1937-10-19 | Alox Corp | Compounded lubricants |
| US2370299A (en) * | 1941-02-26 | 1945-02-27 | Standard Oil Co California | Compounded lubricant |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2493483A (en) * | 1948-04-26 | 1950-01-03 | Shell Dev | Marine engine lubricant |
| US2810744A (en) * | 1955-03-25 | 1957-10-22 | Exxon Research Engineering Co | Polymerization process for preparing lubricant additives and products |
| US3219657A (en) * | 1961-02-27 | 1965-11-23 | Monsanto Co | Saccharide polydicarboxylate half-esters |
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