US2990368A - Lubricating grease compositions containing an alkylaminocarbazole - Google Patents
Lubricating grease compositions containing an alkylaminocarbazole Download PDFInfo
- Publication number
- US2990368A US2990368A US734118A US73411858A US2990368A US 2990368 A US2990368 A US 2990368A US 734118 A US734118 A US 734118A US 73411858 A US73411858 A US 73411858A US 2990368 A US2990368 A US 2990368A
- Authority
- US
- United States
- Prior art keywords
- grease
- inhibitor
- amount
- alkylaminocarbazole
- lubricating grease
- 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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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/041—Carbon; Graphite; Carbon black
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/102—Silicates
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/105—Silica
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- 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
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- 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
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- 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
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- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/16—Naphthenic acids
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- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
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- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- 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
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- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/062—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups bound to the aromatic ring
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- 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
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- 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
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- C10M2215/066—Arylene diamines
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- C10M2215/102—Ureas; Semicarbazides; Allophanates
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- C10M2215/221—Six-membered rings containing nitrogen and carbon only
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- 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—Semi-solids; greasy
Definitions
- This invention relates to the stabilization of synthetic grease and more particularly to a novel method of preventing and/ or retarding deterioration thereof.
- the present application is a continuation-in-part of my earlier'application Serial No. 537,539, filed September 29, 1955, now Patent No. 2,864,676.
- Synethetic greases include lithium base grease, sodium base grease, potassium base grease, calcium base grease, barium base grease, strontium base grease, aluminum base grease, beryllium base grease, cadmium base grease, magnesium base grease, lead soap grease, complex soap grease, etc., or mixtures known as mixed base greases.
- These greases are solid or semi-solid gels and in general are prepared by the addition to mineral oils of hydrocarbon-soluble metal soaps or salts of higher fatty acids as, for example, lithium stearate, calcium stearate, aluminum naphthenate, etc. In another method, the metal soap or salt.
- the grease may contain thickening agents such as silica, carbon black, polyacrylates, talc, polyamides, alkylureas, etc.
- Another type of grease is prepared from oxidized petroleum wax to which the saponifiable base is combined with the proper amount of the desired 's'aponifying agent, and the resultant mixture processed to produce a grease.
- the present invention relates to a method of stabilizing synthetic grease which comprises incorporating therein a stabilizing concentration of an alkylaminocarbazole inhibitor.
- the present invention relates to a method of stabilizing lithium base grease which comprises incorporating therein from about 0.( )001% to about 5% by Weight of 3-octylaminocarbazole.
- the present invention relates to a synthetic grease containing a stabilizing concentration of the inhibitor herein set forth. 7
- stabilization of synthetic grease presents problems considerably different from those encountered in the stabilization of petroleum greases, for example.
- Synthetic greases have been developed for use at high temperatures and therefore require a stabilizing agent which will be'etfective at the high temperatures encountered during use of the synthetic grease.
- the chemical composition of synthetic greases is difi'ferent from the chemical composition of petroleum greases, and these different properties accordingly present different problems. 7
- stabilization of synthetic grease is accomplished by incorporating therein an alkylaminocarbazole inhibitor.
- Illustrative inhibitors include l-ethylaminocarbazole, l-propylaminocarbazole, l-butylaminocarbazole, l-amylaminocarbazole, 1.- hexyla'minocarbazole, l-heptylaminocarbazole, l-octylaminocarbazole, l-nonylaminocarbazole, l-decylaminocarbazole, l-undecylaminocarbazole, l-dodecylarninocarbazole, etc., 3-ethylaminocarbazole, 3-propylaminocarbazole, S-butylaminoca-rbazole, 3-amylaminocarbazole, 3- hexylaminocarbazole, 3-heptylaminocarbazole, 3-octy1- aminocarbazole, 3-nonylaminocarbazole, 3-decylami
- aminocarbazoles also having a substituent attached to the imiuo nitrogen may be used.
- the imino nitrogen is the heterocyclic nitrogen in the S-memberedring.
- Illustrative examples jofin hibitors in this class include N-ethyl-3-ethylaminocarbazole, N-ethyl-S-propylaminocarbazole, .N-ethyl-3-butylj aminocarbazole, N-ethyl-3-amylaminocarbazole, Nwethyl; 3-hexylaminocarbazole, N-ethyl-3-heptylaminocarbazole, N-ethyl-3-octylaminocarbazole, etc., N-propyl-3-ethylaminocarbazole, N-pro'pyl-B-propylaminocarbazole, N- propyl-3-butylaminocarbazole, N-propyl-3-amyl
- the amino or alkylaminotetras hydrocarbazoles may be employed.
- Illustrative examples hatching, etc., 3,6-diethylaminocarbazole, 3,6-dipropylamiof compounds in this class include 6 propylamino-l ,2,3,4- tetrahydrocarbazole, 6-buty1amino-1,2,3,4-tetrahydroqar apel tram, 6-amy1aminol,2,3,4-tetrahydrocarbazole, 6-hex -ylamino-1,2,3,4, tetrahydrocarbazole, etc, v
- alkyl-substituted amino or p'olyaminocarbazoles' are preferred, it-isunders'toodthat substituted amino or' polyamino' c'arbazc les in which the substituent comprises other groups may be employed.
- the other groups preferably comprise hydrocarbon groups and will be selected from cycloallryl, a'ryl, alkaryl or aralkyl.
- the substituent maycomprise an alkenyl or eycloalkenyl' group.
- the alkyl or'other hydrocarbon group may contain non-hydrocarbon comand/or sulfur.
- mixtures of compounds may be employed. In fact, during the preparation of some of these compounds, '9. mixturecontaining two different 'alkylamino or polyalkylamino compounds is formed, and such mixture may be used.
- the inhibitor compounds of the present invention may be prepared in any suitable manner.
- aminocarbazole may be prepared by nitration of oarbazole to form the nitro-substituted compound, followed by reduc tion of the nitro group tothe amino group and by reductive alkylation to form the alkylarninocanbazole.
- the alkylsubstitution preferably is of secondary configuration; that is, the alkyl group is attached to the nitrogen atom at an intermediate carbon atom of the alkyl group. This substitution is obtained by utilizing a ketone in the reductive alkylation reaction.
- an aldehyde is used in the reductive alkylation step.
- the inhibitor of the present invention is utilized in a concentration of from about 0,0001% to about 5% by weight of the grease.
- concentration to be used will depend upon the particular grease 1 7 being treated. In most cases concentrations of from about v0.01% to about 3% by weight generally is employed.
- the inhibitor may be used along vator as, for example, disalicylal diamino propane, ethylene diamine tetraacetic acid tetrasodiurn salt, etc., or to include other additives such as tricresyl phosphate, trialkyl phenols includingv 2,6-di-tert-butyl-4-methylphenol, 2,4-di-tmethyhfi-tert-butylphenol, etc., alkylated diphenyl phenyl naphthyl amines, dialkyl phenyl ene diamines, phenotbia'zinaorganic selenium compounds, etc.,
- the inhibitor of the present invention may be utilized as such or in a suitable solvent including hydrocarbons, alcohols, glycols, ketones, others, etc.
- the inhibitor may beprepared asa mixture with one or more of these other additives and incorporated'in-this manner ulcerhe grease or components'thereof.
- the inhibitor of the present invention may begincorporated in the grease in any suitable manneriand at any suitable stage of preparation. Thus, it may be added to one Tor more'components of the grease prior to compositing and processing thereof or it may be added to the mix at any time, preferably before final processing in order to obtain intimate mixing and dissolving of the inhibitor in the grease.
- Example I modified Norma-Hoffman method in which a sample of the grease is placed in a bomb and oxygen is charged thereto. The bomb then is heated to 212 F., and the time required for a drop of 5 pounds pressure is taken as the induction period. In this run, a control sample of the grease (not containing this additive) had an induction period of 10 hours. On the other hand, a sample of the grease containing 1% by weight of 3-octylaminocarbazole had an induction period of 3'1 hours. Thus, it is seen that the inhibitor of the present invention served to improved considerably the stability of the grease.
- Example 11 The run described in Example I was continued until a pressure drop of 30 pounds per square inch was obtained. In the control sample, this drop occurred after 23 hours. However, the sample containing 3-octylaminocarbazole ran for 122 hours before reaching the 30 pound pressure drop.
- Example III The inhibitor of this example is 3-isopropylaminocarbazole. This compound has a melting point of 181"- .182 C. and a boiling point of 190 C. at 1 mm. pressure. This additive is incorporated in a calcium base grease in 'a concentration of 0.5% by weight and serves to increase the time required for a drop of five pounds pressure when the grease is evaluated in the modified Norma-Hofiman method described in Example 1.
- Example IV The inhibitor of this example is 3,-6-diisopropylaminocarbazole, which compound has a boiling point of 170- 230 C. at 1 mm. pressure. 1.5% by weight of this inhibitor is incorporated in sodium base grease and serves to increase the time required for a drop of 5 pounds pressure when the grease is evaluated in the modified Norma-Hofiman method described in Example I;
- Example V thickening amount of a metal soap of a higher fatty acid and a stabilizing concentration of analkylaminocarbazole inhibitor.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a metal soap of a higher fatty acid and a stabilizing concentration of a polyalkylaminooarbazole inhibitor.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of an alkylamino carbazole inhibitor.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of a polyalkylaminocarbazole inhibitor.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of 1-(2-octylaminocarbazole).
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of 3-octylaminocarbazole.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of 3-isopropylamino carbazole.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of 3,6-diisopropy1- aminocanbazole.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a calcium soap of a higher fatty acid and a stabilizing concentration of 3-octylaminocarbazole.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a calcium soap of a higher fatty acid and a stabilizing concentration of 3-isopropylaminocarbazole.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of lithium stearate and from about 0.0001% to about 5% by weight of an alkylaminocarbazole inhibitor.
- a lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of calcium stearate and from about 0.0001% to about 5% by weight of an alkylaminocarbazole inhibitor.
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- Chemical & Material Sciences (AREA)
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- Oil, Petroleum & Natural Gas (AREA)
- Lubricants (AREA)
Description
States Patent 2,990,368 LUBRICATING GREASE COMPOSITIONS CON TAINING AN ALKYLAMINOCARBAZOLE Ralph B Thompson,.Hinsdale, Ill., assignor, by mesne assignments, to Universal Oil Products Company, Des ll Plaines, 111., a corporation of Delaware No Drawing. Filed May 9, 1958, Ser. No. 734,118
. 1 12' Claims. (Cl. 2.'5240.7)
This invention relates to the stabilization of synthetic grease and more particularly to a novel method of preventing and/ or retarding deterioration thereof. The present application is a continuation-in-part of my earlier'application Serial No. 537,539, filed September 29, 1955, now Patent No. 2,864,676.
Synethetic greases include lithium base grease, sodium base grease, potassium base grease, calcium base grease, barium base grease, strontium base grease, aluminum base grease, beryllium base grease, cadmium base grease, magnesium base grease, lead soap grease, complex soap grease, etc., or mixtures known as mixed base greases. These greases are solid or semi-solid gels and in general are prepared by the addition to mineral oils of hydrocarbon-soluble metal soaps or salts of higher fatty acids as, for example, lithium stearate, calcium stearate, aluminum naphthenate, etc. In another method, the metal soap or salt. is added to synthetic oils including, for example, di- (2-ethylhexyl) sebacate or azelate, di-tetradecyl sebacate, tricresyl phosphate, polyalkylene oxides, silicones, alkyl or alkyl aryl polysiloxanes or blends of these with petroleum oil. The grease may contain thickening agents such as silica, carbon black, polyacrylates, talc, polyamides, alkylureas, etc. Another type of grease is prepared from oxidized petroleum wax to which the saponifiable base is combined with the proper amount of the desired 's'aponifying agent, and the resultant mixture processed to produce a grease.
' In one embodiment the present invention relates to a method of stabilizing synthetic grease which comprises incorporating therein a stabilizing concentration of an alkylaminocarbazole inhibitor.
In a specific embodiment the present invention relates to a method of stabilizing lithium base grease which comprises incorporating therein from about 0.( )001% to about 5% by Weight of 3-octylaminocarbazole.
In still another embodiment, the present invention relates to a synthetic grease containing a stabilizing concentration of the inhibitor herein set forth. 7
The stabilization of synthetic grease presents problems considerably different from those encountered in the stabilization of petroleum greases, for example. Synthetic greases have been developed for use at high temperatures and therefore require a stabilizing agent which will be'etfective at the high temperatures encountered during use of the synthetic grease. Furthermore, the chemical composition of synthetic greases is difi'ferent from the chemical composition of petroleum greases, and these different properties accordingly present different problems. 7 In accordance with the present invention stabilization of synthetic grease is accomplished by incorporating therein an alkylaminocarbazole inhibitor. Illustrative inhibitors include l-ethylaminocarbazole, l-propylaminocarbazole, l-butylaminocarbazole, l-amylaminocarbazole, 1.- hexyla'minocarbazole, l-heptylaminocarbazole, l-octylaminocarbazole, l-nonylaminocarbazole, l-decylaminocarbazole, l-undecylaminocarbazole, l-dodecylarninocarbazole, etc., 3-ethylaminocarbazole, 3-propylaminocarbazole, S-butylaminoca-rbazole, 3-amylaminocarbazole, 3- hexylaminocarbazole, 3-heptylaminocarbazole, 3-octy1- aminocarbazole, 3-nonylaminocarbazole, 3-decylaminocarbazole, 3-undecylaminocarbazole, 3-dodecylaminocarnocarbazole, 3,6-dibutylaminocarbazole, 3,6-diamylami nocarbazole, 3,6-dihexylaminocarbazole, 3,6-diheptylami nocarbazole, 3,6-dioctylaminocarbazole, 3,6-dinonylauii nocarbazole, 3,6-didecylaminocarbazole, 3,6-diundecyla minocarbazole, 3,6-didodecylaminocarbazole,etc., 1,3,63,- tetraethylaminocarbazole, 1,3,,8-tetrapopylaminocanbazole, l,3,6,8-tetrabutylaminocarbazole, 1,3,6,8-tetraam ylaminocarbazole, 1,3,6,8-tetrahexylaminocarbazole, 1,3,6 8 tetraheptylaminocarbazole, 1,3,6,8-tetracotylami n 0 cat I,- bazole, etc. 2,3,6,7-tetraethylaminocarbazole,; 2 ,3, 6,- 7.,- aminocarbazole, 2,3,6,7 -tetrapropylamino c a r b ;a z o l e, 2,3,6,7-tetrabutylaminocarbazole, 2,,3,6,7-tetraamylaminocarbazole, 2,3,6,7wtetrahexylaminocarbazole, 2,3,6,7-tetra} heptylaminocarbazole, 2,3,6,7 tetraoctylaminocarbazole, etc, It is understood that the specificcompounds set forth above are illustrative and that correspondingcompounds having the substitutions in other positions may be utilized. q
In another embodiment, aminocarbazoles also having a substituent attached to the imiuo nitrogen may be used. The imino nitrogen is the heterocyclic nitrogen in the S-memberedring. Illustrative examples jofin hibitors in this class include N-ethyl-3-ethylaminocarbazole, N-ethyl-S-propylaminocarbazole, .N-ethyl-3-butylj aminocarbazole, N-ethyl-3-amylaminocarbazole, Nwethyl; 3-hexylaminocarbazole, N-ethyl-3-heptylaminocarbazole, N-ethyl-3-octylaminocarbazole, etc., N-propyl-3-ethylaminocarbazole, N-pro'pyl-B-propylaminocarbazole, N- propyl-3-butylaminocarbazole, N-propyl-3-amylaminocarbazole, N-propyl-Shexylaminocarbazole, N-propyl-3- heptylaminocarbazole, N-propyl-3-octy1aminocarbazole, etc., N-buty1-3-ethylaminocarbazole, N-butyl-3-propylaminocarbazole, N-butyl-3-butylaminocarbazole, N-butyl- 3-amy1aminocarbaz0le, N-bu-tyl-3.-hexylaminocarbazole, N-butyl-3-heptylaminocarbazole, N-butyl-3-octylaminocarbazole, etc., N-amyl-3-ethylaminocarbazole, N-amyl- 3-propylaminocarbazole, N-amyl-3-butylarninocarbazole, N-amyLS-amylaminocarbazole, N-amyl-3 hexylaminocar bazole, N-amyI-S-heptylaminocarbazole, N-amyl-3-octylaminocarbazole, etc., N-hexyl-3-ethylaminocarbazole, N hexyl-B-propylaminocarbazole, N-hexyl-3-butylaminocar bazole, N-hexyl-3-amylaminocarbazole, N-hexyl-B-hexylaminooarbazole, N-hexyl 3 heptylaminocarbazole,--N- hexyl 3 octyl'aminocarbazole, etc., N ethyl 3,6- dipropylaminocarbazole, N propyl 3,6 dipropylaminocarbazole, N-butyl-3,6-dipropylaminocarbazole, N- amyl 3,6-dipropylaminocarbazole, N-hexyl-3,6-dipropyl aminocarbazole, etc., N-ethyl-2,3,6,7-tetraethylaminocare bazole, N-ethy1-2,3,6,7-tetrapropylaminocarbazole, N ethyl-2,3,6,7-tetrabutylaminocarbazole, N-ethyl-2,3, 6,7- tetraamylaminocarbazole, N-ethyl-,2,3,6,7-tetrahexy1ami nocarbazole, etc., N-propyl 2,3,6,7-'t etraethylarninocarbazole, N-propyl-Z,3,6,T-tetrapropylaminocarbazole, N- propyl-2,3,6,7-tetrabutylaminocarbazole, N-propyl-2,3,6,7- tetraamylamiuocarbazole, N-propyl-2,3,6,7-tetrahexylaminocarbazole, etc., N-pr'opyl 1,3,6,8-tetrapropylaminocarbazole, N-propyl 1,3,6,8-tetrabutylaminocarbazole, etc. Here again, it is understood that the specific compounds set forth above are illustrative and that other compounds containing an alkyl substituent attached to the imino nitrogen and also those containing this substituent and alkyl substituents attached to one or more of the amino nitrogens may be employed.
In another embodiment, the amino or alkylaminotetras hydrocarbazoles may be employed. Illustrative examples bazole, etc., 3,6-diethylaminocarbazole, 3,6-dipropylamiof compounds in this class include 6 propylamino-l ,2,3,4- tetrahydrocarbazole, 6-buty1amino-1,2,3,4-tetrahydroqar bazole, 6-amy1aminol,2,3,4-tetrahydrocarbazole, 6-hex -ylamino-1,2,3,4, tetrahydrocarbazole, etc, v
While the alkyl-substituted amino or p'olyaminocarbazoles' are preferred, it-isunders'toodthat substituted amino or' polyamino' c'arbazc les in which the substituent comprises other groups may be employed. The other groups preferably comprise hydrocarbon groups and will be selected from cycloallryl, a'ryl, alkaryl or aralkyl. In some cases, the substituent maycomprise an alkenyl or eycloalkenyl' group. In still other cases, the alkyl or'other hydrocarbon group may contain non-hydrocarbon comand/or sulfur.
It is understood" that mixtures of compounds may be employed. In fact, during the preparation of some of these compounds, '9. mixturecontaining two different 'alkylamino or polyalkylamino compounds is formed, and such mixture may be used.
It is apparent that numerous compounds may be prepared andutilized in accordance with the present invention; However, all of these compounds are not necesponents including those comprising oxygen, nitrogen sarily'equivalent and maybe oi diiferent effectiveness in the same or different greases. The particular compound The particular carbazole compound illustrated is a 3- alkylaminocarbazole. Again, it is understood that this formula is merely for illustrative purposes and that other suitable alkylamino, including poly-substituted compounds, may be employed.
The inhibitor compounds of the present invention may be prepared in any suitable manner. For example, aminocarbazole may be prepared by nitration of oarbazole to form the nitro-substituted compound, followed by reduc tion of the nitro group tothe amino group and by reductive alkylation to form the alkylarninocanbazole. The alkylsubstitution preferably is of secondary configuration; that is, the alkyl group is attached to the nitrogen atom at an intermediate carbon atom of the alkyl group. This substitution is obtained by utilizing a ketone in the reductive alkylation reaction. When a primary group is. desired, an aldehyde is used in the reductive alkylation step. 1 In general the inhibitor of the present invention is utilized in a concentration of from about 0,0001% to about 5% by weight of the grease. The exact concentration to be used will depend upon the particular grease 1 7 being treated. In most cases concentrations of from about v0.01% to about 3% by weight generally is employed.
with other additives incorporated in synthetic grease, including alcohols, esters, organic amines, polybutene, sul-furized fatty materials, sulfur chlorine compounds, dyes, perfumed materials, fillers, etc. In some cases, it may be of advantage to also include a metal deacti- It is understood that the inhibitor may be used along vator as, for example, disalicylal diamino propane, ethylene diamine tetraacetic acid tetrasodiurn salt, etc., or to include other additives such as tricresyl phosphate, trialkyl phenols includingv 2,6-di-tert-butyl-4-methylphenol, 2,4-di-tmethyhfi-tert-butylphenol, etc., alkylated diphenyl phenyl naphthyl amines, dialkyl phenyl ene diamines, phenotbia'zinaorganic selenium compounds, etc.,
7 "2,990,368 i is? 4 as well as corrosion inhibitors, extreme pressure additives, viscosity index improvers, etc. The inhibitor of the present invention may be utilized as such or in a suitable solvent including hydrocarbons, alcohols, glycols, ketones, others, etc. When desired, the inhibitor may beprepared asa mixture with one or more of these other additives and incorporated'in-this manner irithe grease or components'thereof. a
The inhibitor of the present invention may begincorporated in the grease in any suitable manneriand at any suitable stage of preparation. Thus, it may be added to one Tor more'components of the grease prior to compositing and processing thereof or it may be added to the mix at any time, preferably before final processing in order to obtain intimate mixing and dissolving of the inhibitor in the grease.
The following examples are introduced to illustrate further the novelty and utility of the present invention but not with the intention of unduly limiting the same.
Example I modified Norma-Hoffman method, in which a sample of the grease is placed in a bomb and oxygen is charged thereto. The bomb then is heated to 212 F., and the time required for a drop of 5 pounds pressure is taken as the induction period. In this run, a control sample of the grease (not containing this additive) had an induction period of 10 hours. On the other hand, a sample of the grease containing 1% by weight of 3-octylaminocarbazole had an induction period of 3'1 hours. Thus, it is seen that the inhibitor of the present invention served to improved considerably the stability of the grease.
Example 11 The run described in Example I was continued until a pressure drop of 30 pounds per square inch was obtained. In the control sample, this drop occurred after 23 hours. However, the sample containing 3-octylaminocarbazole ran for 122 hours before reaching the 30 pound pressure drop.
Example III The inhibitor of this example is 3-isopropylaminocarbazole. This compound has a melting point of 181"- .182 C. and a boiling point of 190 C. at 1 mm. pressure. This additive is incorporated in a calcium base grease in 'a concentration of 0.5% by weight and serves to increase the time required for a drop of five pounds pressure when the grease is evaluated in the modified Norma-Hofiman method described in Example 1.
Example IV The inhibitor of this example is 3,-6-diisopropylaminocarbazole, which compound has a boiling point of 170- 230 C. at 1 mm. pressure. 1.5% by weight of this inhibitor is incorporated in sodium base grease and serves to increase the time required for a drop of 5 pounds pressure when the grease is evaluated in the modified Norma-Hofiman method described in Example I;
Example V thickening amount of a metal soap of a higher fatty acid and a stabilizing concentration of analkylaminocarbazole inhibitor.
2. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a metal soap of a higher fatty acid and a stabilizing concentration of a polyalkylaminooarbazole inhibitor.
3. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of an alkylamino carbazole inhibitor.
4. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of a polyalkylaminocarbazole inhibitor.
5. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of 1-(2-octylaminocarbazole).
6. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of 3-octylaminocarbazole.
7. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of 3-isopropylamino carbazole.
8. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a lithium soap of a higher fatty acid and a stabilizing concentration of 3,6-diisopropy1- aminocanbazole.
9. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a calcium soap of a higher fatty acid and a stabilizing concentration of 3-octylaminocarbazole.
10. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of a calcium soap of a higher fatty acid and a stabilizing concentration of 3-isopropylaminocarbazole.
11. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of lithium stearate and from about 0.0001% to about 5% by weight of an alkylaminocarbazole inhibitor.
12. A lubricating grease composition consisting essentially of a major amount of a lubricating oil, a greasethickening amount of calcium stearate and from about 0.0001% to about 5% by weight of an alkylaminocarbazole inhibitor.
References Cited in the file of this patent UNITED STATES PATENTS 1,836,702 Christmann Dec. 15, 1931 2,370,552 Lincoln et a1. Feb. 27, 1945 2,374,098 Ingram Apr. 17, 1945 2,595,140 Heinrich Apr. 29, 1952 2,607,735 Sproule et a1. Aug. 19, 1952 2,652,366 Jones et a1. Sept. 15, 1953
Claims (1)
1. LUBRICATING GREASE COMPOSITION CONSISTING ESSENTIALLY OF A MAJOR AMOUNT OF A LIBRICATING OIL, A GREASE THICKENING AMOUNT OF METAL SOAP OF A HIGHER FATTY ACID AND STABILIZING CONCENTRATION OF AN ALKYLAMINO CARBAZOLE INHIBITOR.
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US734118A US2990368A (en) | 1958-05-09 | 1958-05-09 | Lubricating grease compositions containing an alkylaminocarbazole |
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WO2023098954A1 (en) * | 2021-12-02 | 2023-06-08 | Continental Reifen Deutschland Gmbh | Compound, rubber blend containing the compound, vehicle tire comprising the rubber blend in at least one component, process for producing the compound, and use of the compound as an age resistor and/or antioxidant |
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US2607735A (en) * | 1949-03-12 | 1952-08-19 | Standard Oil Dev Co | Alkaline earth metal soap greases |
US2652366A (en) * | 1950-08-15 | 1953-09-15 | Shell Dev | Method of preparing lubricating grease compositions |
US2595140A (en) * | 1950-12-01 | 1952-04-29 | Standard Oil Dev Co | Oxidation resistant lubricating oil composition |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001051479A2 (en) * | 2000-01-07 | 2001-07-19 | Warner-Lambert Company | Tricyclic compounds with antiviral activity |
WO2001051479A3 (en) * | 2000-01-07 | 2002-02-14 | Warner Lambert Co | Tricyclic compounds with antiviral activity |
US6800656B2 (en) | 2000-01-07 | 2004-10-05 | Warner Lambert Company | Tricyclic compounds and method of treating herpes virus |
US20050075332A1 (en) * | 2000-01-07 | 2005-04-07 | Warner Lambert Company | Tricyclic compounds with antiviral activity |
WO2023098954A1 (en) * | 2021-12-02 | 2023-06-08 | Continental Reifen Deutschland Gmbh | Compound, rubber blend containing the compound, vehicle tire comprising the rubber blend in at least one component, process for producing the compound, and use of the compound as an age resistor and/or antioxidant |
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