US3799876A - Corrosion inhibiting lubrication method - Google Patents
Corrosion inhibiting lubrication method Download PDFInfo
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- US3799876A US3799876A US00097362A US9736270A US3799876A US 3799876 A US3799876 A US 3799876A US 00097362 A US00097362 A US 00097362A US 9736270 A US9736270 A US 9736270A US 3799876 A US3799876 A US 3799876A
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- 238000005260 corrosion Methods 0.000 title abstract description 29
- 230000007797 corrosion Effects 0.000 title abstract description 29
- 238000000034 method Methods 0.000 title abstract description 19
- 230000002401 inhibitory effect Effects 0.000 title abstract description 14
- 238000005461 lubrication Methods 0.000 title description 8
- -1 METHYL GROUP Chemical group 0.000 abstract description 16
- 239000010687 lubricating oil Substances 0.000 abstract description 14
- 239000001257 hydrogen Substances 0.000 abstract description 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 9
- 239000003112 inhibitor Substances 0.000 abstract description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 5
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 abstract description 4
- 239000007788 liquid Substances 0.000 abstract description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 150000003254 radicals Chemical class 0.000 abstract 3
- 239000012530 fluid Substances 0.000 description 19
- 125000004432 carbon atom Chemical group C* 0.000 description 13
- 239000000203 mixture Substances 0.000 description 12
- 239000002253 acid Substances 0.000 description 8
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 8
- 239000012808 vapor phase Substances 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 6
- 239000002199 base oil Substances 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- 150000002431 hydrogen Chemical group 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 4
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- FKDRSGGLIDRWBW-UHFFFAOYSA-N 1-(tert-butylamino)ethanol Chemical compound CC(O)NC(C)(C)C FKDRSGGLIDRWBW-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid group Chemical group C(CCCCCC)(=O)O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000010688 mineral lubricating oil Substances 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VHBZLDYGXAEIDU-UHFFFAOYSA-N 1-(cyclohexylamino)ethanol Chemical compound CC(O)NC1CCCCC1 VHBZLDYGXAEIDU-UHFFFAOYSA-N 0.000 description 1
- LEYYLQKYOZYCRF-UHFFFAOYSA-N 1-(hexylamino)ethanol Chemical compound CCCCCCNC(C)O LEYYLQKYOZYCRF-UHFFFAOYSA-N 0.000 description 1
- UQJDVLPHTXQTRP-UHFFFAOYSA-N 2,2-bis(heptanoyloxymethyl)butyl heptanoate Chemical compound CCCCCCC(=O)OCC(CC)(COC(=O)CCCCCC)COC(=O)CCCCCC UQJDVLPHTXQTRP-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 description 1
- 101150009724 CYBA gene Proteins 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- VLGUBUHHNFCMKI-UHFFFAOYSA-N aminomethoxymethanamine Chemical compound NCOCN VLGUBUHHNFCMKI-UHFFFAOYSA-N 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical class CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical class CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 239000010723 turbine oil 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M133/08—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy 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
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic 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
- C10M2207/282—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
- C10M2207/283—Esters of polyhydroxy compounds
-
- 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
- C10M2207/286—Esters of polymerised unsaturated 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
-
- 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
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
Definitions
- R is an alkyl radical having from 3 to 10 carbon atoms
- R is hydrogen, an alkyl radical having 1 to 8 carbon atoms, or in conjunction with R a cyclohexyl radical
- Y is an alkylene radical having from 2 to 3 carbon atoms
- R" is hydrogen or a methyl group.
- a novel method for lubricating and for inhibiting corrosion in a power system wherein integral parts of the system or metal surfaces are intermittently exposed in an atmosphere which is corrosive or permits corrosion to occur has now been developed.
- This method is based on the employment of a lubricating oil containing a specific class of alkylaminoalkanols therein.
- the specific alkylaminoalkanols function as vapor phase corrosion inhibitors in power systems. Since these corrosion inhibitors are vaporized under conditions present in power systems, they 3,799,876 Patented Mar. 26, 1974 ice are effective for protecting all of the metallic components of the system during normal operation periods as well as when the equipment is at rest.
- the lubricating fluid retains its corrosion inhibiting properties for an extended period of time as required of such fluids.
- the class of additives do not adversely effect the acidity or neutralization properties of the carrier fluid.
- the vapor phase corrosion inhibiting method of this invention is effective when employed in conjunction with a wide variety of lubricating oils.
- the inhibitors may be employed in both mineral and synthetic types of lubricating oils and may also be employed with other conventional lubricating oil additives.
- R is an alkyl radical having from 3 to 10 carbon atoms
- R is hydrogen, an alkyl radical having 1 to 8 carbon atoms, or in conjunction with R a cyclohexyl radical
- Y is an alkylene radical having from 2 to 3 carbon atoms
- R" is hydrogen or a methyl group.
- the preferred compounds are those in which R has 3 to 6 carbon atoms, R is hydrogen, Y is a divalent ethylene radical and R" is hydrogen.
- Typical compounds which are effective as vapor phase corrosion inhibitors in the lubrication method of the invention include t-butylaminoethanol, n-hexylaminoethanol, cyclohexylaminoethanol, 1,3-dimethylbutylaminoethanol, n-pentylaminopropanol-Z, n-butylaminopropanol-2, and n-hexylaminoethyl methyl ether.
- the fluids which can be employed in preparing a lubricating oil for the method of this invention include both mineral and synthetic oils of lubricating viscosities.
- the hydrocarbon mineral oils usable in this invention can be distillate or residual oils. Paraffin base distillate lubricating oil fractions are preferred for the formulation of premium engine oils.
- the lubricating oil base generally has been subjected to solvent refining to improve its lubricity and viscosity temperature relationship as -well as solvent dewaxing to remove waxy components and improve the pour of the oil.
- mineral lubricating oils having an SUS viscosity at F. between 50 and 1000 may be used in the formulation of the improved lubricants of this invention although the viscosity range will usually fall between 70 and 500 SUS at 100 F.
- a blend of base oils can be employed to provide a suitable base for multigrade oils.
- a suitable synthetic fluid is an ester base fluid prepared from pentaerythritol or trimethylolpropane and a mixture of hydrocarbyl monocarboxylic acids.
- Polypentaerythritols such as dipentaerythritol, tripentaerythritol and tetra-pentaerythritol can also be employed in the reaction to prepare the base oil.
- the hydrocarbon monocarboxylic acids which are used to form the ester-base fluid include the straight-chain and branched-chain aliphatic acids, cycloaliphatic acids and aromatic acids as well as mixtures of these acids.
- the acids employed have from about 2 to 18 carbon atoms per molecule, and preferably from about 5 to 10 carbon atoms. Examples of suitable specific acids are acetic, prohour interval. A rating of no rust to trace rust for this test shows that the method employing the indicated fluid was outstanding in providing vapor phase corrosion inhibition. Several individual runs were made for certain specific fluids.
- pentaerythritol tetraesters include pentaerythritol and crude caproic acid containing other C monobasic acids.
- Another suitable tetraester is prepared from a technical grade pentaerythritol and a mixture of acids comprising 38 percent valeric, 13 percent Z-methyl pentanoic, 32 percent octanoic and 17 percent pelargonic acids.
- Another effective ester is the triester of trimethylolpropane in which the trimethylolpropane is esterified with a monobasic acid mixture consisting of 2 percent valeric, 9 percent caproic, 13 percent heptanoic, 7 percent heptanoic, 7 percent octanoic, 3 percent caprylic, 65 percent pelargonic and 1 percent capric acids.
- Trimethylolpropane triheptanoate, trimethylolpropanepentanoate and trimethylolpropanehexanoate are also suitable ester bases.
- the fluid employed in the method of the invention comprises a substantial proportion of the base oil and a minor corrosion inhibiting amount of the alkylaminoalkanol defined above. Corrosion inhibiting amounts of the alkylaminoalkanol are readily dissolved in the base fluid. In general, from about 0.01 to 5 weight percent of the alkylaminoalkanol is dissolved in the base oil to provide an eflective corrosion inhibiting method although larger amounts can also be employed. The preferred concentration range is from 0.10 to 1.5 weight percent.
- the examples in Table 1 below illustrate preferred lubricant embodiments for use in the method of the invention.
- the base fluid was a blend of refined mineral oils. Specifically the base oil consisted of a 30 percent. to 70 percent blend of 145 SUS and 600 SUS at 100 F. parafiinic pale turbine oils. The corrosion inhibitors were blended into the base fluid and the latter tested in the method of the invention.
- the test employed was a modified version of the Shell Reflux Rust Test wherein the modification involved replacing the hot plate with a constant temperature oil bath maintained ta 210 F.
- the metal test specimens were inspected at one and two hour intervals as well as at the usual 20 The foregoing test results show that the method of the invention is outstandingly effective for providing extended vapor phase corrosion inhibition required by many kinds of power systems.
- R is an alkyl radical having from 3 to 10 carbon atoms
- R is hydrogen, an alkyl radical having from 1 to 8 carbon atoms or a cyclohexyl radical
- Y is an alkylene radical having from 2 to 3 carbon atoms.
- alkylaminomethylether is n-hexylaminoethylmethylether.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
METHOD FOR INHIBITING CORROSION IN A POWER SYSTEM CONTAINING A LUBRICATING OIL AND WHEREIN METALLIC MEMBERS OF THE SYSTEM ARE ONLY INTERMITTENLY CONTACT WITH THE LIQUID LUBRICATING OIL AND ARE SUSCEPTIBLE TO CORROSION COMPRISING ADDING AN ALKYLAMINOALKANOL OR ALKYLAMINOMETHYLETHER CORROSION INHIBITOR OT THE LUBRICATING OIL, SAID ALKYLAMINOALKANOL OR ALKULAMINOMETHYLETHER HAVING THE FORMULA:
RR''N--Y--OR
IN WHICH R IS AN ALKYL RADICAL HAVING FROM 3 TO 10 CARBON ATOMS, R7 IS HYDROGEN, AN ALKYL RADICAL HAVING 1 TO 8 CARBON ATOMS, OR IN INJUNCTION WITH R A CYCLOHEXYL RADICAL, Y IS AN ALKYLENE RADICAL HAVING FROM 2 TO 3 CARBON ATOMS ARE R" IS HYDROGEN OR A METHYL GROUP.
RR''N--Y--OR
IN WHICH R IS AN ALKYL RADICAL HAVING FROM 3 TO 10 CARBON ATOMS, R7 IS HYDROGEN, AN ALKYL RADICAL HAVING 1 TO 8 CARBON ATOMS, OR IN INJUNCTION WITH R A CYCLOHEXYL RADICAL, Y IS AN ALKYLENE RADICAL HAVING FROM 2 TO 3 CARBON ATOMS ARE R" IS HYDROGEN OR A METHYL GROUP.
Description
United States Patent O 3,799,876. CORROSION INHIBITING LUBRICATION METHOD James A. White, Groves, and Ralph P. Chesluk, Nederland, Tex., assignors to Texaco Inc., New York, NY. No Drawing. Filed Dec. 11, 1970, Ser. No. 97,362
Int. Cl. Cm 1/20, 1/32 US. Cl. 252-515 R 2 Claims ABSTRACT OF THE DISCLOSURE Method for inhibiting corrosion in a power system containing a: lubricating oil and wherein metallic members of the system are only intermittently contacted with the liquid lubricating oil and are susceptible to corrosion comprising adding an alkylarninoalkanol or alkyl' aminomethylether corrosion inhibitor to the lubricating oil, said alkylaminoalkanol or alkylaminomethylether having the formula:\
in which R is an alkyl radical having from 3 to 10 carbon atoms, R is hydrogen, an alkyl radical having 1 to 8 carbon atoms, or in conjunction with R a cyclohexyl radical, Y is an alkylene radical having from 2 to 3 carbon atoms and R" is hydrogen or a methyl group.
BACKGROUND OF THE INVENTION Field of the invention In the lubrication and operation of power systems wherein a fluid is employed for lubrication, cooling and/ or for transmitting power, such as in internal combustion engines and hydraulic systems, the fluid or lubricant is not continuously in contact with the metallic parts of the engine or hydraulic system. This condition is particularly pronounced when the power system is not in use since the fluid drains into a reservoir in a lower part of the equipment leaving parts of the power system exposed to the prevailing atmospheric envoronments. It will be appreciated that when the power system is in operation, the fluid will generally provide a satisfactory level of lubrication protecting the system from wear and corrosion. However, during intermittent operations or during the periods when the system is at rest, the fluid is ineffective for providing a satisfactory level of corrosion protection. This is particularly true under conditions in which corrosive gases or substantial amounts of water vapor come in contact with important parts of the power equipment. A method of lubrication which inhibits or prevents the corrosion of the equipment under the foregoing condition has now been developed.
Description of the prior art US. Pat. 2,775,560 discloses a lubricant containing a socalled vapor phase corrosion inhibiting agent. The particular agent is a low molecular weight aliphatic monocarboxylic acid containing from 8 to 10 carbon atoms in the molecule.
SUMMARY OF THE INVENTION A novel method for lubricating and for inhibiting corrosion in a power system wherein integral parts of the system or metal surfaces are intermittently exposed in an atmosphere which is corrosive or permits corrosion to occur has now been developed. This method is based on the employment of a lubricating oil containing a specific class of alkylaminoalkanols therein. A particular feature of the invention is that the specific alkylaminoalkanols function as vapor phase corrosion inhibitors in power systems. Since these corrosion inhibitors are vaporized under conditions present in power systems, they 3,799,876 Patented Mar. 26, 1974 ice are effective for protecting all of the metallic components of the system during normal operation periods as well as when the equipment is at rest. Another feature is that the lubricating fluid retains its corrosion inhibiting properties for an extended period of time as required of such fluids. A further feature of the invention is that the class of additives do not adversely effect the acidity or neutralization properties of the carrier fluid.
The vapor phase corrosion inhibiting method of this invention is effective when employed in conjunction with a wide variety of lubricating oils. The inhibitors may be employed in both mineral and synthetic types of lubricating oils and may also be employed with other conventional lubricating oil additives.
DESCRIPTION OF PREFERRED EMBODIMENTS The corrosion inhibiting lubrication method of the invention employs a fluid of lubricating viscosity containing a minor corrosion inhibiting amount of an alkylaminoalkanol or alkylaminomethylether represented by the formula:
in which R is an alkyl radical having from 3 to 10 carbon atoms, R is hydrogen, an alkyl radical having 1 to 8 carbon atoms, or in conjunction with R a cyclohexyl radical, Y is an alkylene radical having from 2 to 3 carbon atoms and R" is hydrogen or a methyl group. The preferred compounds are those in which R has 3 to 6 carbon atoms, R is hydrogen, Y is a divalent ethylene radical and R" is hydrogen.
Typical compounds which are effective as vapor phase corrosion inhibitors in the lubrication method of the invention include t-butylaminoethanol, n-hexylaminoethanol, cyclohexylaminoethanol, 1,3-dimethylbutylaminoethanol, n-pentylaminopropanol-Z, n-butylaminopropanol-2, and n-hexylaminoethyl methyl ether. Mixtures of these compounds such as a 3/1 mixture of monoand diheptyla-minoethanol have been observed to provide advantages over the use of a single corrosion inhibitor, a mixture of n-heptylarninoethanol and n-hexylaminopropanol-Z is also suitable.
The fluids which can be employed in preparing a lubricating oil for the method of this invention include both mineral and synthetic oils of lubricating viscosities. The hydrocarbon mineral oils usable in this invention can be distillate or residual oils. Paraffin base distillate lubricating oil fractions are preferred for the formulation of premium engine oils. The lubricating oil base generally has been subjected to solvent refining to improve its lubricity and viscosity temperature relationship as -well as solvent dewaxing to remove waxy components and improve the pour of the oil. Generally, mineral lubricating oils having an SUS viscosity at F. between 50 and 1000 may be used in the formulation of the improved lubricants of this invention although the viscosity range will usually fall between 70 and 500 SUS at 100 F. A blend of base oils can be employed to provide a suitable base for multigrade oils.
A suitable synthetic fluid is an ester base fluid prepared from pentaerythritol or trimethylolpropane and a mixture of hydrocarbyl monocarboxylic acids. Polypentaerythritols, such as dipentaerythritol, tripentaerythritol and tetra-pentaerythritol can also be employed in the reaction to prepare the base oil.
The hydrocarbon monocarboxylic acids which are used to form the ester-base fluid include the straight-chain and branched-chain aliphatic acids, cycloaliphatic acids and aromatic acids as well as mixtures of these acids. The acids employed have from about 2 to 18 carbon atoms per molecule, and preferably from about 5 to 10 carbon atoms. Examples of suitable specific acids are acetic, prohour interval. A rating of no rust to trace rust for this test shows that the method employing the indicated fluid was outstanding in providing vapor phase corrosion inhibition. Several individual runs were made for certain specific fluids.
TABLE I.--VAPOR PHASE RUST TEST Concentra- Busting rate, hours tion, wt. Example Inhibitor percent 1 2 20 1 t-Butylaminoethanol 1. 2N R, T N R, 2T NR, 2T 2 do 0.50 3NR BNR NR, 2T
0. 3T 2T, L 2'1, L 1. 00 3NR 3NR 3NR 0.50 3NR 3NR 2NR, 'I 0. 10 BT T, 2L '1, 2L 1. 00 3NR 3NR 3N 0.50 2NR, T 2NR, T 3T 0. l0 2T T, L L/M, M 1.00 3T T 3T 0.50 2NR, T 2NR, T 2NR, T 0. 10 3NR 3NR 3NR 1. 00 T T T 0. 50 T T T 1. 00 NR NR T 0. 50 T T L 0.10 T L M 1.00 NR,T NR,T NR,T 0.50 NR,T NR,T NR,T 0. 10 NR T T 1. 00 BNR 3NR NR, 2T 0.50 1. 00 R R N 0. 50 l. 00 0.50 1. 00 0. 50 0.10 1. 00 0. 50 0. 10
L 34 Decanoie acid 0. 10 BNR 1 Base oil is /70 145PPTO/600PPTO. LEGEND.-NR=I1O rust; T=trace, few pln points; L=light rust; S=severe, pitting, heavy rust; M=rnoderate rust.
propane with the preferred ester bases being the pentaerythritol tetraesters include pentaerythritol and crude caproic acid containing other C monobasic acids. Another suitable tetraester is prepared from a technical grade pentaerythritol and a mixture of acids comprising 38 percent valeric, 13 percent Z-methyl pentanoic, 32 percent octanoic and 17 percent pelargonic acids. Another effective ester is the triester of trimethylolpropane in which the trimethylolpropane is esterified with a monobasic acid mixture consisting of 2 percent valeric, 9 percent caproic, 13 percent heptanoic, 7 percent heptanoic, 7 percent octanoic, 3 percent caprylic, 65 percent pelargonic and 1 percent capric acids. Trimethylolpropane triheptanoate, trimethylolpropanepentanoate and trimethylolpropanehexanoate are also suitable ester bases.
The fluid employed in the method of the invention comprises a substantial proportion of the base oil and a minor corrosion inhibiting amount of the alkylaminoalkanol defined above. Corrosion inhibiting amounts of the alkylaminoalkanol are readily dissolved in the base fluid. In general, from about 0.01 to 5 weight percent of the alkylaminoalkanol is dissolved in the base oil to provide an eflective corrosion inhibiting method although larger amounts can also be employed. The preferred concentration range is from 0.10 to 1.5 weight percent.
The examples in Table 1 below illustrate preferred lubricant embodiments for use in the method of the invention. In each of these examples the base fluid was a blend of refined mineral oils. Specifically the base oil consisted of a 30 percent. to 70 percent blend of 145 SUS and 600 SUS at 100 F. parafiinic pale turbine oils. The corrosion inhibitors were blended into the base fluid and the latter tested in the method of the invention. The test employed was a modified version of the Shell Reflux Rust Test wherein the modification involved replacing the hot plate with a constant temperature oil bath maintained ta 210 F. In addition, the metal test specimens were inspected at one and two hour intervals as well as at the usual 20 The foregoing test results show that the method of the invention is outstandingly effective for providing extended vapor phase corrosion inhibition required by many kinds of power systems.
We claim:
1. In a power system comprised of metallic conduit and friction creating sliding surfaces susceptible to corrosion normally containing a liquid lubricating oil having an SUS viscosity at F. between 70 and 500 and wherein the lubricant is only intermittently in contact with parts of the metallic surfaces, the method of inhibiting corosion in said system which comprises employing a. mineral lubricating oil containing from about 0.01 to 5.00 weight percent of an alkylaminomethylether having the formula:
in which R is an alkyl radical having from 3 to 10 carbon atoms, R is hydrogen, an alkyl radical having from 1 to 8 carbon atoms or a cyclohexyl radical, and Y is an alkylene radical having from 2 to 3 carbon atoms.
2. A method according to claim 1 in which said alkylaminomethylether is n-hexylaminoethylmethylether.
References Cited UNITED STATES PATENTS 2,189,788 2/1940 Freeman 2525l.5 R 2,780,598 2/1957 Cafcas 25234.7 X 3,280,029 10/1966 Waldmann 25277 3,372,009 3/1968 Waldmann 4472 3,527,804 9/1970 Cyba 25251.5 R
DANIEL E. WYMANN, Primary Examiner W. J. SHINE, Assistant Examiner US. Cl. X.R 25277, 392
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US00097362A US3799876A (en) | 1970-12-11 | 1970-12-11 | Corrosion inhibiting lubrication method |
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US00097362A US3799876A (en) | 1970-12-11 | 1970-12-11 | Corrosion inhibiting lubrication method |
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US3799876A true US3799876A (en) | 1974-03-26 |
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US00097362A Expired - Lifetime US3799876A (en) | 1970-12-11 | 1970-12-11 | Corrosion inhibiting lubrication method |
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4062764A (en) * | 1976-07-28 | 1977-12-13 | Nalco Chemical Company | Method for neutralizing acidic components in petroleum refining units using an alkoxyalkylamine |
US4229284A (en) * | 1978-05-15 | 1980-10-21 | Nalco Chemical Co. | Corrosion control method using methoxypropylamine (mopa) in water-free petroleum and petrochemical process units |
US4477362A (en) * | 1981-03-18 | 1984-10-16 | The Lubrizol Corporation | Method for preparing nitrogen- and oxygen-containing compositions _useful as lubricant and fuel additives |
US4599090A (en) * | 1981-03-18 | 1986-07-08 | The Lubrizol Corporation | Method for preparing nitrogen- and oxygen-containing compositions useful as lubricant and fuel additives |
EP0192358A2 (en) * | 1985-02-04 | 1986-08-27 | Ge Chemicals, Inc. | Metal working fluid composition |
EP0196810A2 (en) * | 1985-03-29 | 1986-10-08 | Borg-Warner Corporation | Process and kit for working metals |
US4749503A (en) * | 1986-03-07 | 1988-06-07 | Chemical Exchange Industries, Inc. | Method and composition to control microbial growth in metalworking fluids |
US5773393A (en) * | 1991-09-16 | 1998-06-30 | The Lubrizol Corporation | Oil compositions useful in hydraulic fluids |
US20040204326A1 (en) * | 2003-04-08 | 2004-10-14 | Crompton Corporation | Anti-oxidants in soluble oil base for metal working fluids |
US20210161829A1 (en) * | 2015-12-22 | 2021-06-03 | Modernatx, Inc. | Compounds and compositions for intracellular delivery of agents |
-
1970
- 1970-12-11 US US00097362A patent/US3799876A/en not_active Expired - Lifetime
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4062764A (en) * | 1976-07-28 | 1977-12-13 | Nalco Chemical Company | Method for neutralizing acidic components in petroleum refining units using an alkoxyalkylamine |
US4229284A (en) * | 1978-05-15 | 1980-10-21 | Nalco Chemical Co. | Corrosion control method using methoxypropylamine (mopa) in water-free petroleum and petrochemical process units |
US4477362A (en) * | 1981-03-18 | 1984-10-16 | The Lubrizol Corporation | Method for preparing nitrogen- and oxygen-containing compositions _useful as lubricant and fuel additives |
US4599090A (en) * | 1981-03-18 | 1986-07-08 | The Lubrizol Corporation | Method for preparing nitrogen- and oxygen-containing compositions useful as lubricant and fuel additives |
EP0192358A3 (en) * | 1985-02-04 | 1987-10-14 | Borg-Warner Chemicals Inc. | Metal working fluid composition |
EP0192358A2 (en) * | 1985-02-04 | 1986-08-27 | Ge Chemicals, Inc. | Metal working fluid composition |
EP0196810A2 (en) * | 1985-03-29 | 1986-10-08 | Borg-Warner Corporation | Process and kit for working metals |
EP0196810A3 (en) * | 1985-03-29 | 1987-10-28 | Borg-Warner Corporation | Process and kit for working metals |
US4749503A (en) * | 1986-03-07 | 1988-06-07 | Chemical Exchange Industries, Inc. | Method and composition to control microbial growth in metalworking fluids |
US5773393A (en) * | 1991-09-16 | 1998-06-30 | The Lubrizol Corporation | Oil compositions useful in hydraulic fluids |
US20040204326A1 (en) * | 2003-04-08 | 2004-10-14 | Crompton Corporation | Anti-oxidants in soluble oil base for metal working fluids |
US7569526B2 (en) | 2003-04-08 | 2009-08-04 | Crompton Corporation | Anti-oxidants in soluble oil base for metal working fluids |
US20210161829A1 (en) * | 2015-12-22 | 2021-06-03 | Modernatx, Inc. | Compounds and compositions for intracellular delivery of agents |
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