US2854410A - Soap-thickened lubricating greases containing an alcohol-substituted amide - Google Patents
Soap-thickened lubricating greases containing an alcohol-substituted amide Download PDFInfo
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- US2854410A US2854410A US372179A US37217953A US2854410A US 2854410 A US2854410 A US 2854410A US 372179 A US372179 A US 372179A US 37217953 A US37217953 A US 37217953A US 2854410 A US2854410 A US 2854410A
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- United States
- Prior art keywords
- grease
- soap
- oil
- greases
- lubricating
- 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
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- 150000001408 amides Chemical class 0.000 title claims description 17
- 230000001050 lubricating effect Effects 0.000 title claims description 15
- 239000004519 grease Substances 0.000 claims description 27
- 239000000344 soap Substances 0.000 claims description 14
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 10
- 239000000194 fatty acid Substances 0.000 claims description 10
- 229930195729 fatty acid Natural products 0.000 claims description 10
- 150000004665 fatty acids Chemical class 0.000 claims description 10
- 239000010687 lubricating oil Substances 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 239000003921 oil Substances 0.000 description 24
- 235000019198 oils Nutrition 0.000 description 24
- 239000003381 stabilizer Substances 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 239000002480 mineral oil Substances 0.000 description 7
- 125000002947 alkylene group Chemical group 0.000 description 6
- 235000010446 mineral oil Nutrition 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 235000011121 sodium hydroxide Nutrition 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000007859 condensation product Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000010411 cooking Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 230000035900 sweating Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000013556 antirust agent Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 229910001864 baryta Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- -1 ethylene, propylene, butylene Chemical group 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- CKQVRZJOMJRTOY-UHFFFAOYSA-N octadecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O CKQVRZJOMJRTOY-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable 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
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- 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
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated derivatives
-
- 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
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
-
- 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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/042—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds between the nitrogen-containing monomer and an aldehyde or ketone
-
- 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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/043—Mannich bases
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/06—Groups 3 or 13
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
Definitions
- the present invention relates to improved lubricating greases. More particularly, the invention refers to lubricating greases of improved stability at high temperatures and under the influence of mechanical Working. In brief compass, the invention pertains to lubricating greases containing a small stabilizing proportion of the condensation product of an alkylene oxide with an amine or amide of a fatty acid.
- alkali soap base greases In the manufacture of alkali soap base greases, it is possible to prevent the sweating of the oil during storage or working by adding certain compounds, such as naphthenates or arylalkylsulphonates of sodium.
- the present invention relates to a process for preparing greases which possess good stability at high temperatures and under the influence of mechanical stresses and which will remain perfectly stable and homogeneous even when undergoing violent cooling.
- the proportion of stabilizers is in the region of 0.1-%, preferably 0.1-2%, and highly refined oils with a high viscosity index are generally used.
- R and R are aliphatic or aromatic hydrocarbon radicals and x and y are whole numbers.
- the amines and amides used for preparing these products can be aliphatic or aromatic, primary or secondary amines and amides, and their number of carbon atoms may range from 10 to 24. Particularly advantageous are the fatty amines and amides derived from corresponding fatty materials containing more than 10 carbon atoms, such as stearine, tallow, coconut, soya, etc.
- the alkylene oxides or polyoxyalkylenes to be reacted with the amines and amides are oxides of ethylene, propylene, butylene, etc., having preferably 2-6 carbon atoms, or the corresponding polyoxides.
- bracketed alkylene group for the given example of ethylene oxide only contains 2 carbon atoms.
- 3 carbon atoms would be obtained with'proly to vary between about 300 and 7000.
- polyalkylene groups have hydroxylated terminal groups which are capable ofbeing esterified or etherified by conventional methods.
- the lubricating oils used according to the invention may be of mineral or synthetic origin, having a Saybolt viscosity at 37.8 C. of from -2000 seconds, preferably of -1000 seconds and a viscosity index ranging from 0-160, but preferably above 60.
- the soaps to be dispersed in an oil having lubricating properties adequate for the contemplated use are preferably alkali metal soaps, and particularly those of sodium and lithium which tend to form greases with a sufficiently high pour point. They may be present in the grease in proportions of 3-30% by weight of total grease, depend-ing on the final characteristics it is desired to obtain.
- the fatty materials to be saponified are preferably saturated or unsaturated long-chain fatty acids.
- the fats themselves, such as triglycerides, may likewise be used, as well as the fatty acids obtained from hydrogenated animal, marine or vegetable oils or fats or those obtained by the oxidation of hydrocarbons, these fatty acids having a number of carbon atoms ranging from 8-40.
- an anti-oxidant such as phenyl alpha-'naphthylamine or otherwell known oxidation inhibitors, generally in proportions of 0.1-2%. It is, of course, obvious that other addition products, such as tackiness agents, antirust agents, extreme pressure agents and others may likewise be incorporated in suitable proportions, as is well known in the art.
- the greases composed in accordance with the invention may be prepared by the usual processes of mixing, heating and cooling.
- the fatty acid and stabilizing agents described above are added to all or part of the selected mineral oil.
- a saponifying agent is added and heating is continued until the mixture is completely dehydrated and melted.
- the grease is then poured in pans and, after cooling, the cakes of grease formed are worked to the desired consistency.
- the stabilizing agent may also be added, if desired, at the end of cooking and before pouring of the grease.
- Such stabilizers may likewise be suitable for improving the stability properties of greases obtained from naphthenic oils or synthetic oils of an aromatic character.
- the fatty acid is saponified with caustic soda, in the presence or absence of the stabilizer, at about 180 C.; cooking is continued to 225 C.; at this temperature, the molten grease is poured into pans and then worked cold to the desired consistency.
- the greases obtained were tested for their A. S. T. M. consistency characteristics and .pour points as follows.
- Example I The stabilizer is the condensation product of amines obtained from soya fatty acids with 5 molecules ethylene oxide (mean molecular weight 494).
- Viscosity Index 9) 78 77. 8 gtabiliier 0. 2
- Example 11 The stabilizer is the same as that used for Example I,
- the mineral oil has a viscosity index of 75 and is more viscous.
- Example III The stabilizer is the condensation product of amides obtained from coconut fatty acids with 50 molecules ethylene oxide (mean molecular-weight 2400).
- the stabilizer is the condensation product of amines obtained from tallow fatty acids and 15 molecules ethylene oxide (mean molecular weight 930).
- Viscosity Index ) 81.5 81. 25 Stabilizer 0. 25 Properties:
- Example IVb it will be found that owing to the incorporation into the grease of 0.25% stabilizer, there is obtained upon cooling a prefectly homogeneous cake of grease, which does not sweat oil and which, after working, gives a grease having all the desired properties.
- small quantities of various soaps may be introduced, such as aluminum, calcium, barium soap, etc. or very small proportions of a neutralizing base (lime, baryta, etc.) to alter the properties of the grease in the desired direction.
- a neutralizing base such as aluminum, calcium, barium soap, etc. or very small proportions of a neutralizing base (lime, baryta, etc.) to alter the properties of the grease in the desired direction.
- a lubricating grease comprising a major proportion of a lubricating oil having a viscosity in the range of 90- 1000 S. S. U. at 37.8 C. and a viscosity index of 60-160, in the range of 3-30 wt. percent of a grease-making alkali metal soap of a high molecular weight fatty acid and in the range of 0.1-5 wt. percent of an amide having the general formula:
- R is an aliphatic hydrocarbon radical having from to 24 carbon atoms and wherein x and y are Whole numbers, the molecular weight of said amide being between 300 and 7000.
- a lubricating grease comprising a major portion of a lubricating oil, a minor grease making proportion of an alkali metal soap base thickener and containing between 0.1 and 5.0 weight percent of an aliphatic substituted amide having a molecular weight between about 300 and 7,000 derived from a carboxylic acid having from 10 to 24 carbon atoms and having each of the nitrogen valencies linked to an ether alcohol having a terminal hydroxyl group.
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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)
Description
Unite SOAP-THICKENED LUBRICATING GREASES CON-'- TG AN ALCOHOL-SUBSTITUTED AMIDE No Drawing. Application August 3, 1953 Serial No. 372,179
Claims priority, application France December 12, 1952 7 Claims. (Cl. 25242.1)
The present invention relates to improved lubricating greases. More particularly, the invention refers to lubricating greases of improved stability at high temperatures and under the influence of mechanical Working. In brief compass, the invention pertains to lubricating greases containing a small stabilizing proportion of the condensation product of an alkylene oxide with an amine or amide of a fatty acid.
It is well known that in certain uses of greases, for instance in the lubrication of ball or roller bearings operating at high speed or under very high stresses, few greases retain their consistency and their structure. Indeed, the poor lubricating properties of the oils generally used cause rapid heating of the bearings, which results in a destruction of the structure of the grease; the oil then separates from the soap and runs off the bearings under the action of the centrifugal force.
It is well accepted that the lubricating properties of a grease depend mainly on the properties of the oil entering into its composition. The heating of a bearing, for instance, will be less if the oil possesses a suitable viscosity at the temperature at which it is used and a high viscosity index. It is, therefore, desirable in many cases to use lubricating greases containing oils having a high viscosity index.
However, it is Well known that when using paraflinic oils in the preparation of greases with an alkali soap base, and more specifically of sodium greases, it is very diflicult to avoid the separation of the soap from the oil and to obtain stable greases even with very slow cooling. In the case of rapid cooling, for example by pouring the liquefied grease at a temperature above its pour point in a thin layer on plates, a considerable degree of sweating of the oil and a separation of practically all the soap from the oil will be observed. This phenomenon is less pronounced if the mineral oils used are of naphthenic composition.
In the manufacture of alkali soap base greases, it is possible to prevent the sweating of the oil during storage or working by adding certain compounds, such as naphthenates or arylalkylsulphonates of sodium.
The present invention relates to a process for preparing greases which possess good stability at high temperatures and under the influence of mechanical stresses and which will remain perfectly stable and homogeneous even when undergoing violent cooling. These and other results are obtained in accordance with the invention by adding, particularly to alkali soap greases, certain stabilizing and dispersing agents formed mainly by condensation of amines and amides with alkylene oxides.
According to another characteristic, the proportion of stabilizers is in the region of 0.1-%, preferably 0.1-2%, and highly refined oils with a high viscosity index are generally used.
Other advantages and characteristics of the invention will appear more clearly from the description hereinafter in which a number of examples for obtaining greases will Patent Patented Sept. 30, 1958 and amides with alkylene oxides, may be illustrated by the following formulae, if for instance, ethylene oxide is taken as the basis.
(1) Hydroxyaminopolyalkylene compounds:
(2) Hydroxyam ide-polyalkylene compounds:
In the above formulae, R and R are aliphatic or aromatic hydrocarbon radicals and x and y are whole numbers.
The amines and amides used for preparing these products can be aliphatic or aromatic, primary or secondary amines and amides, and their number of carbon atoms may range from 10 to 24. Particularly advantageous are the fatty amines and amides derived from corresponding fatty materials containing more than 10 carbon atoms, such as stearine, tallow, coconut, soya, etc.
The alkylene oxides or polyoxyalkylenes to be reacted with the amines and amides are oxides of ethylene, propylene, butylene, etc., having preferably 2-6 carbon atoms, or the corresponding polyoxides.
Thus, it will be seen from the formulae given above that the bracketed alkylene group for the given example of ethylene oxide only contains 2 carbon atoms. In the same way, 3 carbon atoms would be obtained with'proly to vary between about 300 and 7000. Finally, the
polyalkylene groups have hydroxylated terminal groups which are capable ofbeing esterified or etherified by conventional methods.
Furthermore, the lubricating oils used according to the invention may be of mineral or synthetic origin, having a Saybolt viscosity at 37.8 C. of from -2000 seconds, preferably of -1000 seconds and a viscosity index ranging from 0-160, but preferably above 60.
The soaps to be dispersed in an oil having lubricating properties adequate for the contemplated use are preferably alkali metal soaps, and particularly those of sodium and lithium which tend to form greases with a sufficiently high pour point. They may be present in the grease in proportions of 3-30% by weight of total grease, depend-ing on the final characteristics it is desired to obtain. The fatty materials to be saponified are preferably saturated or unsaturated long-chain fatty acids. The fats themselves, such as triglycerides, may likewise be used, as well as the fatty acids obtained from hydrogenated animal, marine or vegetable oils or fats or those obtained by the oxidation of hydrocarbons, these fatty acids having a number of carbon atoms ranging from 8-40.
Finally, it is advantageous, though not indispensable, to use an anti-oxidant such as phenyl alpha-'naphthylamine or otherwell known oxidation inhibitors, generally in proportions of 0.1-2%. It is, of course, obvious that other addition products, such as tackiness agents, antirust agents, extreme pressure agents and others may likewise be incorporated in suitable proportions, as is well known in the art.
The greases composed in accordance with the invention may be prepared by the usual processes of mixing, heating and cooling. Thus, the fatty acid and stabilizing agents described above are added to all or part of the selected mineral oil. After heating to a temperature sufficient to obtain a homogeneous mixture, a saponifying agent is added and heating is continued until the mixture is completely dehydrated and melted. The grease is then poured in pans and, after cooling, the cakes of grease formed are worked to the desired consistency.
The stabilizing agent may also be added, if desired, at the end of cooking and before pouring of the grease.
It should also be noted that such stabilizers may likewise be suitable for improving the stability properties of greases obtained from naphthenic oils or synthetic oils of an aromatic character.
In the following examples basically the same grease manufacturing and testing methods were used as follows. The fatty acid is saponified with caustic soda, in the presence or absence of the stabilizer, at about 180 C.; cooking is continued to 225 C.; at this temperature, the molten grease is poured into pans and then worked cold to the desired consistency. The greases obtained were tested for their A. S. T. M. consistency characteristics and .pour points as follows.
(1) The percentage of oil separted from the grease after remaining for 50 hours in a drying cabinet at 100 C. In this test, 100 g. grease are placed in a fine mesh, conical metal sieve placed above a calibrated container.
(2) Resistance to mechanical working by measurement of the consistency after 100,000 strokes in the mechanical worker.
Example I The stabilizer is the condensation product of amines obtained from soya fatty acids with 5 molecules ethylene oxide (mean molecular weight 494).
Percent By Weight Ingredients Stearie Acid t 18 1? Pure Caustic Soda. 3 .5 Phenyl alpha-Naphthylamine 1 1 Mineral Oil (Saybolt Viscosity at 37.8 C.=300,
Viscosity Index=9) 78 77. 8 gtabiliier 0. 2
re r es:
P our Point, C 180 180 A. S. 'I. M. Consistency- After 60 Strokes 300 255 After 100,000 Strokes 390 310 Oil Separated at 100 C. After 50 Hours, Percent" 0 0.2
In test (a) during cooling in the pans, a large portion of the oil separate dfrom the grease containing no stabilizer.
Example 11 The stabilizer is the same as that used for Example I,
but the mineral oil has a viscosity index of 75 and is more viscous.
Percent By Weight Ingredients Stearic Acid 23 18 Pure Caustic Soda 4 3 Phenyl alpha-Naphthylamine 1 1 Mineral Oil (Saybolt Viscosity at 3 8 C Viscosity Index-=75) 72 77. 8 Stabilizer 0.2 Properties:
Pour Point, 0 203 190 A. S. T. M. Oonsistency 60 Strokes 345 260 100,000 Strokes Liquid 320 Oil Separated at C. After 50 Hrs, Percent. 12 0. 5
Example III The stabilizer is the condensation product of amides obtained from coconut fatty acids with 50 molecules ethylene oxide (mean molecular-weight 2400).
Ingredients Percent By Weight Stcaric Acid Z) Caustic Soda 3. 5 Phenyl alpha-Naphthylamine- 1 Mineral Oil (Saybolt Viscosity at 3 Index=102) 76. 1 Stabilizer. 0. 4 Properties:
-Pour Point, 0 200 A. S. T. M. Consistency- 60 Str 265 100,000 Strokes 321 Oil Separated at 100 C. After 50 111-5., Percent 0 Example IV The stabilizer is the condensation product of amines obtained from tallow fatty acids and 15 molecules ethylene oxide (mean molecular weight 930).
, Percent By \Veight Ingredients Stearic Acid" 15 15 Caustic Soda... 2. 5 2.5 Phenyl alpha-Naphthyla me 1 1 Mineral Oil (Saybolt Viscosity at 37.8 C.=150,
Viscosity Index=) 81.5 81. 25 Stabilizer 0. 25 Properties:
Pour Point, C 188 A. S. T. M. Consistency- 60 Strokes 265 100,000 Strokes 315 Oil Separated at 100 C. After 50 Hrs, Perce 0.37
It is impossible to manufacture a grease from the ingredients of Example IVa using an oil of low viscosity and high viscosity index and the recommended method (i. e. pouring the compound into pans). When the grease is poured into the pans it will be found, upon cooling, that the soap and oil have separated entirely.
In Example IVb on the other hand, it will be found that owing to the incorporation into the grease of 0.25% stabilizer, there is obtained upon cooling a prefectly homogeneous cake of grease, which does not sweat oil and which, after working, gives a grease having all the desired properties.
It will be seen from the above examples that by using suitable stabilizing agents as defined, it is possible to make from mineral or synthetic oils of highly varying viscosity and high viscosity index, relatively soft lubricating greases characterized by a high pour point, good stability of consistency under the action of mechanical stress and practically no sweating at a temperature of 100 C.
During cooking of the grease, small quantities of various soaps may be introduced, such as aluminum, calcium, barium soap, etc. or very small proportions of a neutralizing base (lime, baryta, etc.) to alter the properties of the grease in the desired direction.
It is, of course, obvious that the present invention has been described purely for the purpose of illustration and in no sense restrictively, and minor changes may be made without departing from its scope.
What is claimed is:
1. A lubricating grease comprising a major proportion of a lubricating oil having a viscosity in the range of 90- 1000 S. S. U. at 37.8 C. and a viscosity index of 60-160, in the range of 3-30 wt. percent of a grease-making alkali metal soap of a high molecular weight fatty acid and in the range of 0.1-5 wt. percent of an amide having the general formula:
wherein R is an aliphatic hydrocarbon radical having from to 24 carbon atoms and wherein x and y are Whole numbers, the molecular weight of said amide being between 300 and 7000.
2. The grease of claim 1 in which R is the hydrocarbon radical of coconut acid, and x+y=50, said molecular weight being about 2400.
3. A lubricating grease comprising a major portion of a lubricating oil, a minor grease making proportion of an alkali metal soap base thickener and containing between 0.1 and 5.0 weight percent of an aliphatic substituted amide having a molecular weight between about 300 and 7,000 derived from a carboxylic acid having from 10 to 24 carbon atoms and having each of the nitrogen valencies linked to an ether alcohol having a terminal hydroxyl group.
4. The lubricating grease defined in claim 3 wherein said lubricating oil has a Saybolt viscosity between about 90 and 1,000 seconds at 37.5 C. and a Viscosity index between about 60 and 160.
5. The lubricating grease as defined in claim 3 wherein said substituted amide is a product formed by condensing the amide with an alkylene oxide having from 2 to 6 carbon atoms in the molecule.
6. The product defined in claim 5 wherein the alk lene oxide is ethylene oxide.
7. The product defined in claim 6 wherein the amide is condensed with from 5 to molecules of ethylene oxide.
References Cited in the file of this patent UNITED STATES PATENTS 1,970,578 Schoeller et a1 Aug. 21, 1934 2,002,613 Orthner May 28, 1935 2,085,706 Schoeller et al. June 29, 1937 2,445,935 Bondi July 27, 1948 2,475,589 Bondi July 12, 1949 2,545,190 Bondi Mar. 13, 1951
Claims (1)
1. A LUBRICATING GREASE COMPRISING A MAJOR PROPORTION OF A LUBRICATING OIL HAVING A VISCOSITY IN THE RANGE OF 901000 S. S. U. AT 37.8*C. AND A VISCOSITY INDEX OF 60-160, IN THE RANGE OF 3-30 WT. PERCENT OF A GREASE-MAKING ALKALI METAL SOAP OF A HIGH MOLECULAR WEIGHT FATTY ACID AND IN THE RANGE OF 0.1-5 WT. PERCENT OF AN AMIDE HAVING THE GENERAL FORMULA:
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR2854410X | 1952-12-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2854410A true US2854410A (en) | 1958-09-30 |
Family
ID=9689336
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US372179A Expired - Lifetime US2854410A (en) | 1952-12-12 | 1953-08-03 | Soap-thickened lubricating greases containing an alcohol-substituted amide |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2854410A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2976243A (en) * | 1957-11-01 | 1961-03-21 | Exxon Research Engineering Co | Stable calcium acetate-mineral oil dispersion |
| US3446737A (en) * | 1966-08-18 | 1969-05-27 | Exxon Research Engineering Co | Friction reducing additive comprising metal soap solubilized in oil by an ncontaining dispersant |
| EP0903398A3 (en) * | 1997-09-23 | 2000-02-02 | Exxon Research And Engineering Company | Lubricating grease containing alkoxylated amine corrosion inhibitor |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1970578A (en) * | 1930-11-29 | 1934-08-21 | Ig Farbenindustrie Ag | Assistants for the textile and related industries |
| US2002613A (en) * | 1932-02-29 | 1935-05-28 | Gen Aniline Works Inc | Reaction product of an organic acid amide and an alkylene oxide |
| US2085706A (en) * | 1930-11-29 | 1937-06-29 | Ig Farbenindustrie Ag | Derivatives of carboxylic acid amides |
| US2445935A (en) * | 1945-10-31 | 1948-07-27 | Shell Dev | Production of greases |
| US2475589A (en) * | 1947-04-18 | 1949-07-12 | Shell Dev | Lubricating grease composition |
| US2545190A (en) * | 1948-09-14 | 1951-03-13 | Shell Dev | Alkali base lubricating greases |
-
1953
- 1953-08-03 US US372179A patent/US2854410A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1970578A (en) * | 1930-11-29 | 1934-08-21 | Ig Farbenindustrie Ag | Assistants for the textile and related industries |
| US2085706A (en) * | 1930-11-29 | 1937-06-29 | Ig Farbenindustrie Ag | Derivatives of carboxylic acid amides |
| US2002613A (en) * | 1932-02-29 | 1935-05-28 | Gen Aniline Works Inc | Reaction product of an organic acid amide and an alkylene oxide |
| US2445935A (en) * | 1945-10-31 | 1948-07-27 | Shell Dev | Production of greases |
| US2475589A (en) * | 1947-04-18 | 1949-07-12 | Shell Dev | Lubricating grease composition |
| US2545190A (en) * | 1948-09-14 | 1951-03-13 | Shell Dev | Alkali base lubricating greases |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2976243A (en) * | 1957-11-01 | 1961-03-21 | Exxon Research Engineering Co | Stable calcium acetate-mineral oil dispersion |
| US3446737A (en) * | 1966-08-18 | 1969-05-27 | Exxon Research Engineering Co | Friction reducing additive comprising metal soap solubilized in oil by an ncontaining dispersant |
| EP0903398A3 (en) * | 1997-09-23 | 2000-02-02 | Exxon Research And Engineering Company | Lubricating grease containing alkoxylated amine corrosion inhibitor |
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