US2493213A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2493213A US2493213A US625955A US62595545A US2493213A US 2493213 A US2493213 A US 2493213A US 625955 A US625955 A US 625955A US 62595545 A US62595545 A US 62595545A US 2493213 A US2493213 A US 2493213A
- Authority
- US
- United States
- Prior art keywords
- oil
- test
- rust
- emulsion
- water
- 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
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
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
-
- 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
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
-
- 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
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/08—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-nitrogen bonds
-
- 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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/08—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
- C10M2227/082—Pb 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/135—Steam engines or turbines
Definitions
- the present invention is directed to an outstanding mineral oil composition which is substantially free from the aforesaid emulsion and rusting difficulties.
- the mineral oil composition of this invention comprises a mineral oil fraction having in admixture therewith a small amount of a trialkyl-plumbane salt of an aliphatic acid represented by the following general formula:
- R is an alkyl group having from about four to about ten carbon atoms
- R, R and R are either the same or different alkyl groups, and are preferably ethyl groups.
- Closely related compounds are not characterized by both rust and emulsion inhibiting properties, as are those compounds which satisfy the aforesaid general formula. For example, triethyl lead acetate, wherein R is a methyl group, is unsatisfactory as a rust inhibitor; and corresponding compounds wherein R is a lauryl, myristyl, stearyl group or the like are unsatisfactory as emulsion retardants.
- trialkylplumbane salts of aliphatic acids contemplated herein may be prepared by any of the procedures set forth in the chemical literature, typical of which are the methods described by Klippel, J. prakt. Chem, (1) 81, 287, (1881), and by Browne and Reid, J. Am. Chem. Soc. 49, 830-8 (1927).
- the preparation of compounds of this invention are illustrated below in the example wherein the method of Browne and Reid, referred to above, was followed:
- Trz'ethyl lead caproate One mol each of tetraethyl lead and of caproic acid were placed in an Erlenmeyer flask equipped with a reflux condenser. The flask was partially immersed in a water bath and the temperature of the bath was raised to C. A small amount, about 0.1 gram, of silica gel was added to the reactants whereupon a slow evolution of ethane was noted. The temperature was then slowly raised to C. and so maintained for 1 /2 hours. At the end of this period the liberation of ethane had practically ceased. The reaction mixture was a fluid which, upon cooling in an ice-water mixture, solidified to a white, crystalline mass.
- the salts of this invention are generally used in oils in amounts of from about 0.01 per cent to about 1.0 per cent, although preferred concentrations are of the border of 0.01 per cent to about 0 .1 per cent.
- these salts may be used alone in oils and may alsobe used in oils containing one or more additive agents.
- they may be used in oils with pour point depressants, oxidation inhibitors, film strength improving agents, oiliness agents, etc.
- Typical of such addition agents are the wellkrrown phenols, amines,; sulfides, organic compounds containing phosphorus, organic compounds containing ha'logen, and the like.
- a mineral oilcomposition comprising a mineral oil fraction normally permitting rusting of ferrous metal surfaces in contact" therewith in the presence of water, and normally susceptible to emulsion formation in the presence of water. having in admixture therewith a: minor proportion, from about 0.01 per cent toabout 1.0' per cent of triethyllead'caproat'e.
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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. 3, 1950 UNITED s'rres LUBRICANT No Drawing.
Application October 31, 1945, Serial No. 625,955
1 Claim. (01. 2s2 35 This invention has to do with lubricants. More particularly, the present invention has to do with lubricants which, in the presence of water, are likely to emulsify and which, in the presence of water and ferrous metal surfaces, generally fail to retard-orprevent rusting of said surfaces.
As is well known to those familiar with the art, difficulties have been experienced during the operation of steam turbines, and this is particularly true during the initial operation of new steam turbines because of emulsion formation andrusting of the ferrous metal parts. During steam turbine operation, some moisture or water accumulates in the oil system which is designed to lubricate the bearings. When conditions become favorable, the oil and water emulsify, whereupon the high degree of lubricating efficiency required in turbine operation is seriously reduced or-impaired. Y
Additionally, the combination of fresh (not previously used) oil, cleannew metal surfaces and moist conditions of operation of new steam turbines appears to be particularly conducive to rusting difficulties. Particles of rust deposited on or carried to bearing surfaces of small clearance such as the governor, for example, tend to cause sticking which renders them inoperative. In cases of severe rusting, bearings may be injured. This rusting phenomenon is evidently the result of improper or inadequate wetting of the metal surfaces with oil, thus permitting a preferential contact of the metal surfaces with the water which is present.
Numerous materials have been proposed for use in oils subject to the aforesaid shortcomings in order to counteracteither the 'emulsification tendency or the inadequate wetting" effect thereof. Generally, such materials as have been previously proposed may effectively reduce the emulsification tendency of the oil, but are usually in'efiective in retarding rust formation or even accelerate the same. Corresponding materials proposed to correct the rusting action normally characteristic of turbine oils and the like either fail to retard emulsion formation or favor such formation. Further diificulty is introduced when other addition agents are incorporated in mineral oil for the purpose of lowering the pour point of the oil, increasing oiliness, or increasing oxidation resistance Of the oil. In some cases, particularly when pour point depressants are incorporated in the oil, the addition agents have proven undesirable in that they have contributed to emulsion formation.
The present invention is directed to an outstanding mineral oil composition which is substantially free from the aforesaid emulsion and rusting difficulties. The mineral oil composition of this invention comprises a mineral oil fraction having in admixture therewith a small amount of a trialkyl-plumbane salt of an aliphatic acid represented by the following general formula:
RI R tbooR .4. I
wherein R is an alkyl group having from about four to about ten carbon atoms, and R, R and R are either the same or different alkyl groups, and are preferably ethyl groups. Closely related compounds are not characterized by both rust and emulsion inhibiting properties, as are those compounds which satisfy the aforesaid general formula. For example, triethyl lead acetate, wherein R is a methyl group, is unsatisfactory as a rust inhibitor; and corresponding compounds wherein R is a lauryl, myristyl, stearyl group or the like are unsatisfactory as emulsion retardants.
The trialkylplumbane salts of aliphatic acids contemplated herein may be prepared by any of the procedures set forth in the chemical literature, typical of which are the methods described by Klippel, J. prakt. Chem, (1) 81, 287, (1881), and by Browne and Reid, J. Am. Chem. Soc. 49, 830-8 (1927). The preparation of compounds of this invention are illustrated below in the example wherein the method of Browne and Reid, referred to above, was followed:
EXAMPLE Trz'ethyl lead caproate One mol each of tetraethyl lead and of caproic acid were placed in an Erlenmeyer flask equipped with a reflux condenser. The flask was partially immersed in a water bath and the temperature of the bath was raised to C. A small amount, about 0.1 gram, of silica gel was added to the reactants whereupon a slow evolution of ethane was noted. The temperature was then slowly raised to C. and so maintained for 1 /2 hours. At the end of this period the liberation of ethane had practically ceased. The reaction mixture was a fluid which, upon cooling in an ice-water mixture, solidified to a white, crystalline mass. The latter material was filtered on a suction filter and thereafter pressed on a porous plate. The crude product was then taken up in boiling petroleum ether to which a small amount of decolorizing charcoal had been added. Silica gel conthe oil compositions contemplated herein, typical emulsion and rust tests were carried out with a mineral oil and with blends of the mineral on and small amounts of saltsrepresented by the The emulsion tests used were the Herschel demulsibility test ataforesaid general formula.
130 F. described in the Federal Standard Stock Catalogue, VV-L-791a, Method 320.32, F-Gz; and the Steam emulsion test described in the Tag Manual for Inspectors of Petroleum, Test N0. 28, A. S. T. M. (Serial D157-36). These tests are not comparable, since frequently an oil which is quite acceptable in one test will not be acce'pt able in the other. Accordingly, an oil which is to be used in steam turbines, for example, should pass both of these tests. The Herschel demulsibility' test is designed to measure the resistance of an oil to the formation of semi-permanent emulsions with water, and is represented in terms of the demulsibility number, D. N.; improved emulsive properties being indicated by larger demulsibilty numbers. The steam emulsion test is represented in terms of the steam emulsion number, S. E. N. Lower S. E. N. values are indicative of improved emulsive properties inasmuch as the ability of the oil to resist emulsification varies inversely with the S. E. N.
In demonstrating the effectiveness of the salts of this invention, an S. A. E. lubricating oil (S. U. V. of 56 seconds at 210 F.) alone or containing 0.1 per cent of a commercial pour d'epressant (an esterified alkyl-substitu-ted phenol) having an adverse effect on emulsive properties, was used as the base oil. The results of these The rust test used'demonstrates the relative ability of an oil to resist rust formation on ferrous metal surfaces of steam turbines and simulates steam turbine operation. The test consists of inserting a clean steel specimen in 300 cos. of the test oil containing 30. cos. of distilled water, and stirring the oil at l38-142 F. for test periods of the order of two days. The rust formed is noted at the end of the test period. The oil used in the test is a turbine oil having a Saybolt Universal viscosity (S. U. V.) of 150 seconds at F. The results of these tests are set forth in Table II below.
Table II Improving Agent lgf g g Rust Test None .Q Very severe rust in i hr. Trletliyllead caproate; 0. 075 Mild rust in 24 hrs. Triethyllead caproate 0. 1 No rust in 72 hrs.
7 The salts of this invention are generally used in oils in amounts of from about 0.01 per cent to about 1.0 per cent, although preferred concentrations are of the border of 0.01 per cent to about 0 .1 per cent. As indicated-above. these salts" may be used alone in oils and may alsobe used in oils containing one or more additive agents. For example. they may be used in oils with pour point depressants, oxidation inhibitors, film strength improving agents, oiliness agents, etc. Typical of such addition agents are the wellkrrown phenols, amines,; sulfides, organic compounds containing phosphorus, organic compounds containing ha'logen, and the like.
It is to be understood that although the invention has been illustrated hereinabove by certain preferred s'altsand oil blends of" the same, it is not to-be restricted thereto and it tobe broadly construed in the light of the scope of the appended claim.
I claim:
A mineral oilcomposition comprising a mineral oil fraction normally permitting rusting of ferrous metal surfaces in contact" therewith in the presence of water, and normally susceptible to emulsion formation in the presence of water. having in admixture therewith a: minor proportion, from about 0.01 per cent toabout 1.0' per cent of triethyllead'caproat'e.
MARIO S. ALTAMURA.
REFERENCES- CITED The following references are of record in the filev of this patent:
UNITED STATES PATENTS Number Name Date 1,857,761 McCabe May 10,1932 2,236,910 Lin'coli'l et a1 Apr. 1, 1941 2,257,750 Lincoln et a1. Oct. 7, 1941 2,261,888 Rocchini NOV- 4, 1941 2,288,288 Lincoln et al'. June 30, 1942 2,290,413 De Groote' July 21, 1942 2,363,510 Farrington .2 Nov. 28, 1944 2,367,470 Neely et a1. Jan". 16, 1945
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US625955A US2493213A (en) | 1945-10-31 | 1945-10-31 | Lubricant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US625955A US2493213A (en) | 1945-10-31 | 1945-10-31 | Lubricant |
Publications (1)
Publication Number | Publication Date |
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US2493213A true US2493213A (en) | 1950-01-03 |
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US625955A Expired - Lifetime US2493213A (en) | 1945-10-31 | 1945-10-31 | Lubricant |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2594924A (en) * | 1947-07-22 | 1952-04-29 | Robert J Hickin | Partition assembling machine |
US2975137A (en) * | 1955-12-30 | 1961-03-14 | Sun Oil Co | Compression refrigeration working fluid |
US3280035A (en) * | 1963-04-17 | 1966-10-18 | Mobil Oil Corp | Oil compositions containing emulsioninhibiting acetylenic compounds |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1857761A (en) * | 1926-09-27 | 1932-05-10 | Standard Oil Dev Co | Nonsludging oil and method of making the same |
US2236910A (en) * | 1938-07-11 | 1941-04-01 | Continental Oil Co | Synthetic lubricant |
US2257750A (en) * | 1939-05-24 | 1941-10-07 | Continental Oil Co | Lubricating oil |
US2261888A (en) * | 1940-04-05 | 1941-11-04 | Gulf Research Development Co | Steam turbine lubrication |
US2288288A (en) * | 1938-08-26 | 1942-06-30 | Socony Vacuum Oil Co Inc | Lubricating oil |
US2290413A (en) * | 1940-10-11 | 1942-07-21 | Petrolite Corp | Composition of matter and process for preventing water-in-oil type emulsions resulting from acidization of calcareous oil-bearing strata |
US2363510A (en) * | 1942-09-15 | 1944-11-28 | Standard Oil Co California | Compounded oil |
US2367470A (en) * | 1939-06-20 | 1945-01-16 | Standard Oil Co California | Compounded oil |
-
1945
- 1945-10-31 US US625955A patent/US2493213A/en not_active Expired - Lifetime
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1857761A (en) * | 1926-09-27 | 1932-05-10 | Standard Oil Dev Co | Nonsludging oil and method of making the same |
US2236910A (en) * | 1938-07-11 | 1941-04-01 | Continental Oil Co | Synthetic lubricant |
US2288288A (en) * | 1938-08-26 | 1942-06-30 | Socony Vacuum Oil Co Inc | Lubricating oil |
US2257750A (en) * | 1939-05-24 | 1941-10-07 | Continental Oil Co | Lubricating oil |
US2367470A (en) * | 1939-06-20 | 1945-01-16 | Standard Oil Co California | Compounded oil |
US2261888A (en) * | 1940-04-05 | 1941-11-04 | Gulf Research Development Co | Steam turbine lubrication |
US2290413A (en) * | 1940-10-11 | 1942-07-21 | Petrolite Corp | Composition of matter and process for preventing water-in-oil type emulsions resulting from acidization of calcareous oil-bearing strata |
US2363510A (en) * | 1942-09-15 | 1944-11-28 | Standard Oil Co California | Compounded oil |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2594924A (en) * | 1947-07-22 | 1952-04-29 | Robert J Hickin | Partition assembling machine |
US2975137A (en) * | 1955-12-30 | 1961-03-14 | Sun Oil Co | Compression refrigeration working fluid |
US3280035A (en) * | 1963-04-17 | 1966-10-18 | Mobil Oil Corp | Oil compositions containing emulsioninhibiting acetylenic compounds |
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