US2880177A - Lubricating greases thickened with benzidine diazo compounds - Google Patents
Lubricating greases thickened with benzidine diazo compounds Download PDFInfo
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- US2880177A US2880177A US631069A US63106956A US2880177A US 2880177 A US2880177 A US 2880177A US 631069 A US631069 A US 631069A US 63106956 A US63106956 A US 63106956A US 2880177 A US2880177 A US 2880177A
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- bis
- grease
- disazo
- lubricating
- acetyl
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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
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/08—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
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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
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/081—Inorganic acids or salts thereof containing halogen
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/082—Inorganic acids or salts thereof containing nitrogen
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- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/084—Inorganic acids or salts thereof containing sulfur, selenium or tellurium
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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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- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/30—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
- C10M2207/302—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids derived from the combination of monocarboxylic acids, dicarboxylic acids and dihydroxy compounds only and having no free hydroxy or carboxyl groups
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- C10M2207/304—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids derived from the combination of monohydroxy compounds, dihydroxy compounds and dicarboxylic acids only and having no free hydroxy or carboxyl groups
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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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- C10M2209/111—Complex polyesters having dicarboxylic acid centres
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- C10M2209/112—Complex polyesters having dihydric acid centres
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- 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
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- 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
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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
- C10M2215/066—Arylene diamines
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- C10M2215/18—Containing nitrogen-to-nitrogen bonds, e.g. hydrazine
- C10M2215/182—Azo compounds
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- C10M2215/221—Six-membered rings containing nitrogen and carbon only
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- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
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- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
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- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
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- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
Definitions
- N N H Joseph F. Lyons, Wappingers Falls, Paul R. Thomas, N N I Beacon, and Norman R. Odell, Fishkill, N.Y., ore Cm 0 053305 to The Texas Company, New York, N .Y., ll corporation Bls (acetyl-N-phenyloarbamylmethi'l)4,4'-dtsazo-3,3'-dichloroof Delaware with? No Drawing. Application December 28, 1956 m 0003' 9 Claims. (Cl.
- Bls (acetyl-N-mxylylcarbamylmeth 1) 4,4'-disazo-2,2-111- chloro-5,5'-dlmethoxy iphenyl novel class of thickening agents therefor. More particularly it relates to lubricating greases thickened with com- 01 pounds of a class of high melting diazo compounds.
- the diazo compounds which are employed as thickening 40 agents in the greases of this invention are compounds represented by the general formula wherein A is chosen from the group consisting of acylacetarylamide and N-arylpyrazolone radicals and their substituted derivatives, and R and R are hydrogens or 6 (hm hm OCH3 or Cl Subsmuents'
- A is chosen from the group consisting of acylacetarylamide and N-arylpyrazolone radicals and their substituted derivatives, and R and R are hydrogens or 6 (hm hm OCH3 or Cl Subsmuents'
- the acylacetaryx' 0 Bis(1-p-toly1-3-methyl-5-keto-4-pyrazolinyl)4,4'-disazo-3,3'-
- Bis(acetyl N phenylcarbamylrnethyl)4,4 The above class of compounds includes the familiar 7o phenyl;bis(acetyl-N-phenylcarbamylmethyl)4,4-disazo-3, Benzidine Yellows and Vulcan Fast Reds, which are cm- 3' dichlorodiphenyl; bis(propionyl-N-phenylcarbamylployed extensively as rubber pigments.
- the grease preparation may be carried out by merely mixing together the thickener and additives, if any, with the lubricating oil, employing any convenient means to obtain a thorough dispersion of the thickener and additives in the lubricating oil base such as by milling in a colloid millor in a paint mill.
- the mixing may be carried out at ordinary or at elevated temperatures up to about 300 F. g desired in order to dissolve any difllculty soluble addives.
- Synthetic oils such as high molecular weight ethers and esters, including particularly the dicarboxylic acid esters, may be employed very advantageously to produce greases for operation at moderately elevated temperatures in the range from about 300 F. to about 400 F.
- Synthetic oils of these types may very advantageously comprise about 50-100 percent by weight of the oil component of the grease, the remainder being mineral oils or other oils of ditferent types.
- a particularly suitable class of dicarboxylic acid ester oils are those disclosed by R. T. Sanderson in US. 2,628,- 974, obtained by reacting dibasic aliphatic acids with glycols and end blocking the reaction products with monohydric aliphatic alcohols or monocarboxylic aliphatic acids.
- the preferred materials of this character are products obtained by reacting a mono-or polyalkylene glycol with a dicarboxylic acid and a monohydric alcohol, represented by the formula wherein R is an aliphatic group or an aliphatic ether group containing from 4 to 12 carbon atoms, R, is an aliphatic group containing from 1 to 12 carbon atoms, and x is an integer from 1 to 5.
- Example 1 A grease was prepared having the following composition in percent by weight:
- the bis(acetyl N o tolylcarbamylrnethyl)4,4'- disazo-3,3'-dichlorodiphenyl was a concentrated pigment in the form of a powder having an average particle size of about 0.01-0.15 micron in diameter.
- the grease was prepared by mixing together the components with an electric stirrer and finishing by milling with two passes through a Premier Colloid Mill at 0.002 inch clearance.
- the diphenyl-p-phenylenediamine was added to the initial mixture in the form of a solution in the tricresyl phosphate.
- a smooth yellow grease was obtained having excellent lubricating properties generally, including superior high temperature performance properties, as shown by the following tests:
- the high temperature performance test of the foregoing table is a test for determining the performance characteristics of greases in antifriction bearings at elevated temperatures and high rotative speeds.
- the test unit consists essentially of a steel spindle supported on ball bearings in an electrically heated housing and driven by an electric motor connected into an electric circuit containing a low amperage fuse 0.1 ampere below that required for full load running.
- the bearings are Norma- Hotfman ABEC No. 3 grade, and are mounted on a spindle approximately 5% inches apart. A thrust load of 17.5 pounds is applied to the bearings.
- One bearing is used for test purposes and the second hearing, which is not heated, is used as a guide hearing.
- the test consists of operating the test bearing for twenty-four hours at 10,000 r.p.m. and at a temperature of from 250 F. to 450 F. followed by a shutdown and cooling period of two hours, and repeating this cycle until the lubricant fails, which is indicated by rupture of the low amperage fuse in the motor circuit.
- Marlin Rockwell special heat treated high speed tool steel bearings with silver plated bronze retainers are used.
- three grams of the test grease are charged to the test bearing and worked into and around the races and balls.
- the hearing is next rotated both clockwise and counterclockwise for one minute each at 200 r.p.m. and assembled into the test unit.
- the heaters and the motor are then started and the test bearing brought up to the test temperature as rapidly as possible, which requires 1.0 to 1.25 hours, while the spindle is rotated at a speed of 10,000 r.p.m.
- the heaters and motors are shut off for 2 hours, during which the temperature of the test bearing drops to a minimum of 120-130 F.
- the total hours of operation, excluding the two hour shutdown periods, to the failure point is recorded as the "hours to failure.
- Example 2 A grease was prepared consisting of a silicone polymer oil thickened with 20 percent by weight, based on the weight of the composition, of bis(acetyl-N-phenylcarbamyl-methyl)4,4-disazo-3,3'-dichlorodiphenyl in the form of a powder having an average particle size'of about 0.01-0.15 micron in diameter and a measured surface area of about square meters per gram. It
- the silicone polymer oil was a commercial product sold by Dow Corning, Inc. under the trade name of DC-SSO, having a methyl-phenyl ratio of about 0.6 and a viscosity in the range from about 300 to about 400 seconds SU at F.
- the grease preparation was carried out by mixing the oil and thickener and finishing by one pass through a Premier Colloid Mill at 0.002 inch clearance. A soft smooth yellow grease was obtained having a dropping point of over 500 F. and an ASTM worked penetration of 345.
- Example 4 As a further example of the greases of this invention, a grease having the combination of high dropping point, water resistance and superior thermal stability at temperature up to about 400 F. is obtained by means of the following composition in percent by weight:
- the synthetic ester and mineral oil are as described in Example 1.
- a lubricating grease consisting essentially of a lubrieating oil thickened to a grease consistency with a compound having the general formula wherein A is chosen from the group consisting of acylacetarylamide, N-arylpyrazolone, and substituted acylacctarylamide and N-arylpyrazolone groups, and R and 7.
- the grease composition of claim 4 wherein the com- R' are chosen from the group consisting of hydrogen, position contains about 0.5-5 percent by weight of an methyl, methoxy and chlorine. amine oxidation inhibitor and about 1-10 percent by 2.
- the grease composition of claim 1 wherein the weight of an oil-soluble phosphorus acid ester.
- said lubricating oil comprises a silicone polymer oil hav- 8.
- a lubricating grease consisting essentially of a lubriing a viscosity in the lubricating oil viscosity range. eating oil thickened to a grease consistency with bis(acetyl- 3.
- the grease composition of claim 1 wherein the said N phenylcarbamylmethyl)4,4 disazo 3,3 diehlorodilubricating oil consists essentially of a methylphenyl siliphenyl. cone polymer having a viscosity in the range from about 9.
- a lubricating grease consisting essentially of a 300 to about 400 seconds SU at 100 F. methylphenyl silicone polymer having a viscosity of from 4.
- a lubricating grease consisting essentially of alubriabout 300 to about 400 seconds SU at 100' F. thickeating oil thickened to a grease consistency with a comened to a grease consistency by about 15-35% by weight pound having the formula based on the weight of the composition of bis(acetyl-N- wherein R is selected from the group consisting of aliphatic groups and aliphatic ether groups containing from 4 to 12 carbon atoms, R is an aliphatic group containing 10 from 1 to 12 carbon atoms, R, is an aliphatic group containing from 1 to 12 carbon atoms, and x is an integer from 1 to 5.
- R R mom wherein R and R are chosen from the group consisting phenylcarbamylmethyl)4,4' disazo 3,3 dichlorodiof hydrogen, methyl, methoxy and chlorine, and R" is phenyl. hydrogen or one or more lower alkyl groups.
- the grease composition of claim 4 wherein the said lubricating oil comprises about -100 percent of a References Cited in the file of this patent UNITED STATES PATENTS methylphenyl silicone polymer oil having a viscosity in 1 932,577 Eichwedg 1 1 O t, 31, 1933 the range from about to about 900 seconds SU at 2,361,568 Reynolds Oct. 31, 1944 F. 2,604,469 Herrmann July 22, 1952 6.
- the grease composition of claim 4 wherein the said 40 2,791,560 Dilworth et al. May 7, 1957
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Description
Patented the following: LUBRICATING GREASES THICKENED WITH BENZIDINE DIAZO COMPOUNDS 1 Cl 6 OHJIO E0011.
N=N H Joseph F. Lyons, Wappingers Falls, Paul R. Thomas, N N I Beacon, and Norman R. Odell, Fishkill, N.Y., ore Cm 0 053305 to The Texas Company, New York, N .Y., ll corporation Bls (acetyl-N-phenyloarbamylmethi'l)4,4'-dtsazo-3,3'-dichloroof Delaware with? No Drawing. Application December 28, 1956 m 0003' 9 Claims. (Cl. 252-493) This invention relates to lubricating g eases and to a 15 Bis(acetyl'N'phenylcarbmylmemyl)gy'dmzo's'm' methoxydlphenyl CHIC 0 C1 Cl C O CH: H( J-N=N N=N- 'm Qnnc'w (JONEQ CH| CH; 1 CH: Ht
Bls (acetyl-N-mxylylcarbamylmeth 1) 4,4'-disazo-2,2-111- chloro-5,5'-dlmethoxy iphenyl novel class of thickening agents therefor. More particularly it relates to lubricating greases thickened with com- 01 pounds of a class of high melting diazo compounds. H H
We have found that compounds of a class of diazotized benzidine derivatives form stable gels of grease-like con- 80 =0 0= sistency, having very superior lubricating properties, when they are dispersed in lubricating oils in suitable proportions. In particular, high temperature performance pr0perties are obtained in these compositions which are greatly superior to those obtainable in the conventional map 85 thickened greases, and also to those obtainable in other non-soap thickened greases of the prior art, containing Bis(l-phenyl-3-methy1-5-keto-4;pyrazolinyl)4,4'-d1sazo-3.3'- finely divided solids of other types having the property of diqhmmdlphenyl thickening lubricating oils to a grease consistency. R
The diazo compounds which are employed as thickening 40 agents in the greases of this invention are compounds represented by the general formula wherein A is chosen from the group consisting of acylacetarylamide and N-arylpyrazolone radicals and their substituted derivatives, and R and R are hydrogens or 6 (hm hm OCH3 or Cl Subsmuents' The acylacetaryx' 0 Bis(1-p-toly1-3-methyl-5-keto-4-pyrazolinyl)4,4'-disazo-3,3'-
amide and N-arylpyrazolone radicals may contain subdtmethoxydiphenyl H H cnnooc-ooN=N--C N=No-o=co0on1. ILB'\N (i=0 O=C Bis (1-phenyl-8'carboxyethyl-5-keto-4-pyrazollnyl)4,4'-dlsazo- 3,3-dlchlorodipl1euyl stituents of various types such as alkyl, aryl, alkaryl, aralkyl groups, OR", COOR", OH, j-NO -NH --NHR", -NR"R", halogens, etc., where R" this invention include the following: and R' are alkyl or aryl groups. Bis(acetyl N phenylcarbamylrnethyl)4,4 The above class of compounds includes the familiar 7o phenyl;bis(acetyl-N-phenylcarbamylmethyl)4,4-disazo-3, Benzidine Yellows and Vulcan Fast Reds, which are cm- 3' dichlorodiphenyl; bis(propionyl-N-phenylcarbamylployed extensively as rubber pigments. Particularly suitniethyl)4,4'-disazo-3,3'-dimethoxydiphenyl; bis(butyrylmay be employed as thickening agents in accordance with able compounds which are commercially available include Additional examples of compounds of this class which 3 N-phenylcarbamylmethyl)4,4' disazo 3,3 dichlorodiphenyl; bis(acetyl-N-o-chlorophenylcarbamylmethyl)4,4- disazodiphenyl; bis acetyl-N- l -naphthylcarbamylmethyl 4,4'-disazo-3,3'-dichlorodiphenyl; bis(acetyl-N-o-bromophenylcarbamylmethyl)4,4' disazo 3,3 dimethoxydiphenyl; bis(acetyl-N-m-xylylcarbamylmethyl)4,4'-disazo- 3,3 dimethoxydiphenyl; bis(acetyl-N-o-tolylcarbamylmethyl)4,4'-disazo-3,3'-dimethyldiphenyl; bis(acetyl-N- 2,5 dichlorophenylcarbamylmethyl)4,4-disazodiphcnyl; bis(acetyl N xenylcarbamylmethyl)4,4' disazo 3,3- dichlorodiphenyl; bis(acetyl N o nitrophenylcarbamylmethyl)4,4'-disazo-3,3'-dimethoxydiphenyl; bis(acetyl-N- o-methoxyphenylcarbamylmethyl)4,4 disazo 3,3 dichlorodiphenyl; bis(acetyl-N-2,4,6-trimethylphenylcarbamylmethyl)4,4'-disazo-3,3-dichlorodiphenyl; bis(acetyl- N phenylcarbamylmethyl)4,4' disazo 2,2',5,5 tetrachlorodiphenyl; bis(acetyl N o chlorophenylcarbamylmethyl)4,4' disazo 2,2 dichloro 5,5 dimethoxydiphenyl; bis(l-phenyl-3-methyl-5-keto-4-pyrazolinyl)4,4'- disazo-3,3'-dimethyldiphenyl; bis(la-naphthyl-3-ethyI-5- keto 4 pyrazolinyl)4,4' disazo 2,2 dichloro 5,5- dimethyldiphenyl; bis( l-phenyl-3-carboxymethyl-5-keto-4- pyrazolinyl)4,4' disazo-3,3'dimethyldiphenyl; bis( l-pethylphenyl 3 methyl 5 keto 4 pyrazolinyl)4,4- disazo-3,3' dimethoxydiphenyl; bis( l-m-xylyl-3-butyl-5- keto 4 pyrazolinyl)4,4' disazo 2,2',5,5 tetrachlorodiphenyl; bis(l-o-chlorophenyl-3-phenyl-S-keto-pyrazolinyl)4,4-disazodiphenyl; bis( l-p-bromophenyl-3-ethyl-5- keto-4-pyrazolinyl)4,4'-disazodiphenyl; bis(l-o-hydroxyp-nitrophenyl B-methyl 5 keto 4 pyrazolinyl)4,4'- disazo-3,3-dichlorodiphenyl.
The above compounds are either commercially available or readily obtainable by well known methods involving diazotizing benzidine or a substituted benzidine and then coupling the diazotized product with a suitable acylacetarylamide or N-arylpyrazolone, as described for example in German Patent 251,479 (1912).
The compounds are employed in finely divided form, ordinarily in the form of particles below about one micron in diameter, and preferably below about 0.5 micron in diameter, which may be obtained either by suitably controlling the crystallization conditions durlng the preparation, or by fine grinding. They may be employed either in pure form or in the form of the so-called reduced toners, wherein the compounds are deposited upon particles of inert inorganic materials such as SiO A1 TiO BaSO clay, etc. Generally such materials will be present only in minor amounts, such as up to about 10 percent by weight, but larger amounts, up to about 25 percent by weight or higher, may be present if desired. In addition, the compounds may contain small amounts, such as up to about 5 percent by weight, of various metal salts, particularly metal chlorides such as zinc chloride, ferric chloride, stannic chloride, and cadmium chloride, which may enter into the crystal structure in some manner which is not entirely understood when such salts are present in the reaction mixture during the crystallization.
The greases of this invention comprise essentially lubricating oils containing sufiicient amounts of thickening agents of the type described above to impart at least substantial thickening. Ordinarily the composition will contain from about 5 to about 45 percent by weight of a thickening agent of this type, and preferably about 15 to about 35 percent by weight of such thickening agent, based on the weight of the composition.
The grease preparation may be carried out by merely mixing together the thickener and additives, if any, with the lubricating oil, employing any convenient means to obtain a thorough dispersion of the thickener and additives in the lubricating oil base such as by milling in a colloid millor in a paint mill. The mixing may be carried out at ordinary or at elevated temperatures up to about 300 F. g desired in order to dissolve any difllculty soluble addives.
The lubricating oils employed in these greases may be any suitable oils of lubricating characteristics, including the conventional mineral lubricating oils, synthetic oils obtained by various refinery processes, such as cracking and polymerization, and other synthetic oleaginous compounds. Suitable mineral oils include paratfinic and naphthenic oils, particularly those having viscosities in the range from about to about 600 seconds SU at 100 F. The preferred class of lubricating oils are the silicone oils, which may be employed in accordance with this invention to produce greases having superior high temperature performance properties at temperatures above about 400 F. Other synthetic oils, such as high molecular weight ethers and esters, including particularly the dicarboxylic acid esters, may be employed very advantageously to produce greases for operation at moderately elevated temperatures in the range from about 300 F. to about 400 F. Synthetic oils of these types may very advantageously comprise about 50-100 percent by weight of the oil component of the grease, the remainder being mineral oils or other oils of ditferent types.
A particularly suitable class of dicarboxylic acid ester oils are those disclosed by R. T. Sanderson in US. 2,628,- 974, obtained by reacting dibasic aliphatic acids with glycols and end blocking the reaction products with monohydric aliphatic alcohols or monocarboxylic aliphatic acids. The preferred materials of this character are products obtained by reacting a mono-or polyalkylene glycol with a dicarboxylic acid and a monohydric alcohol, represented by the formula wherein R is an aliphatic group or an aliphatic ether group containing from 4 to 12 carbon atoms, R, is an aliphatic group containing from 1 to 12 carbon atoms, and x is an integer from 1 to 5.
The silicone oils are compounds having the general wherein R represents alkyl, aryl, alkaryl or aralkyl groups, which may be the same or different, and n is a number sufficient to give a viscosity in the lubricating oil range to the compound, preferably a viscosity in about the range from 70 to 900 seconds Saybolt Universal at 100' F. Suitable compounds of this type include dimethyl silicone polymer, diethyl silicone polymer, methylcyclohexyl silicone polymer, diphenyl silicone polymer, methylethyl silicone polymer, methyltolyl silicone polymer, etc. These materials may be prepared by various methods, including the hydrolysis of hydrolyzable organic-substituted silanes, as described, for example, in US. 2,410,346 and US. 2,469,888.
Additives of the usual types may be employed in these greases, such as, for example, oxidation inhibitors, corrosion inhibitors, tackiness agents, extreme pressure agents, and so forth. An oxidation inhibitor is preferably employed, which may be suitably an inhibitor of the amine type, such as diphenylamine, alphanaphthylamine, beta-naphthylamine, p-phenylene diamine, or N,N' diphenyl-p-phenylene diamine. Acompound of this type may be present in amounts from about 0.5 to about 5 percent by weight based on the weight of the composition. Very advantageously the composition may also contain about 1-10 percent by weight of an oil-soluble phosphorus acid ester, which may serve as a carrier and dispersing agent for the amine inhibitor. Also, additional thickening agents may be employed, such as other finely divided solids of various types and metal soaps of high molecular weight fatty acids, such as are conventionally employed in lubricating greases.
The following examples are given for the purpose of more fully disclosing the invention.
mesons? Example 1 A grease was prepared having the following composition in percent by weight:
The bis(acetyl N o tolylcarbamylrnethyl)4,4'- disazo-3,3'-dichlorodiphenyl was a concentrated pigment in the form of a powder having an average particle size of about 0.01-0.15 micron in diameter.
The synthetic ester was obtained by reacting together sebacic acid, 2-ethylhexane-1,3-diol, and 2 ethylhexanol in about a 2:1:2 ratio, respectively, and consisting predominantly of the compound (iS-C H17)O0C- (CHQr-COO iso-C I-I OOC-(CH -COO-(iso- 3 The mineral oil was a refined paraflinic distillate oil having a viscosity of about 330 seconds Saybolt Universal at 100 F. t
The grease was prepared by mixing together the components with an electric stirrer and finishing by milling with two passes through a Premier Colloid Mill at 0.002 inch clearance. The diphenyl-p-phenylenediamine was added to the initial mixture in the form of a solution in the tricresyl phosphate. A smooth yellow grease was obtained having excellent lubricating properties generally, including superior high temperature performance properties, as shown by the following tests:
Dropping point, "F 500+ Working stability, penetration at 77 R After 60 strokes 311 After 100,000 strokes 341 1 slze worker, slze cone. The high temperature performance test of the foregoing table is a test for determining the performance characteristics of greases in antifriction bearings at elevated temperatures and high rotative speeds. The test unit consists essentially of a steel spindle supported on ball bearings in an electrically heated housing and driven by an electric motor connected into an electric circuit containing a low amperage fuse 0.1 ampere below that required for full load running. The bearings are Norma- Hotfman ABEC No. 3 grade, and are mounted on a spindle approximately 5% inches apart. A thrust load of 17.5 pounds is applied to the bearings. One bearing is used for test purposes and the second hearing, which is not heated, is used as a guide hearing. The test consists of operating the test bearing for twenty-four hours at 10,000 r.p.m. and at a temperature of from 250 F. to 450 F. followed by a shutdown and cooling period of two hours, and repeating this cycle until the lubricant fails, which is indicated by rupture of the low amperage fuse in the motor circuit. In carrying out the test at 400 F. or above, Marlin Rockwell special heat treated high speed tool steel bearings with silver plated bronze retainers are used. In starting up the test, three grams of the test grease are charged to the test bearing and worked into and around the races and balls. The hearing is next rotated both clockwise and counterclockwise for one minute each at 200 r.p.m. and assembled into the test unit. The heaters and the motor are then started and the test bearing brought up to the test temperature as rapidly as possible, which requires 1.0 to 1.25 hours, while the spindle is rotated at a speed of 10,000 r.p.m.
After 24 hours of operation the heaters and motors are shut off for 2 hours, during which the temperature of the test bearing drops to a minimum of 120-130 F. The total hours of operation, excluding the two hour shutdown periods, to the failure point is recorded as the "hours to failure.
Example 2 A grease was prepared consisting of a silicone polymer oil thickened with 20 percent by weight, based on the weight of the composition, of bis(acetyl-N-phenylcarbamyl-methyl)4,4-disazo-3,3'-dichlorodiphenyl in the form of a powder having an average particle size'of about 0.01-0.15 micron in diameter and a measured surface area of about square meters per gram. It
contained 1.31 percent of zinc in the form of a soluble zinc salt.
The silicone polymer oil was a commercial product sold by Dow Corning, Inc. under the trade name of DC-SSO, having a methyl-phenyl ratio of about 0.6 and a viscosity in the range from about 300 to about 400 seconds SU at F.
The grease preparation was carried out by mixing the oil and thickener and finishing by one pass through a Premier Colloid Mill at 0.002 inch clearance. A soft smooth yellow grease was obtained having a dropping point of over 500 F. and an ASTM worked penetration of 345.
This grease ran for 968 hours at 400 F. in the high temperature performance test described above. This is far in excess of the high temperature performance life obtained with the best solids thickened greases of the prior art. For example, a grease of the same grade, consisting of DC-550 thickened with 30 percent by weight of finely divided indigo, ran for only 378 hours at 400 F. in this test under the same conditions.
Example 3 the following test results:
Dropping point, F. 500+ Working stability, A.S.T.M. penetration at 77 F.:
After 60 strokes 284 After 100,000 strokes 335 A.S.T.M. bomb oxidation test, 100 hrs. at 210 F.,
lbs. pressure drop 9-12 Dynamic water resistance, percent loss 0 Example 4 As a further example of the greases of this invention, a grease having the combination of high dropping point, water resistance and superior thermal stability at temperature up to about 400 F. is obtained by means of the following composition in percent by weight:
Bis( 1 phenyl 3 methyl 5 keto 4 pyrazolinyl)4,4 disazo 3,3 dichlorodiphenyl 20.0 Diphenyl-p-phenylenediamine 1.0 Tricresyl phosphate 3.0 Mineral oil 5.0 Synthetic ester 71.0
The synthetic ester and mineral oil are as described in Example 1.
Obviously many modifications and variations of the invention, as hereinbefore set forth, may be made without departing from the spirit and scope thereof and therefore, only such limitations should be imposed as are lubricating oil comprises about 50-100 percent of a polyindicated in the appended claims. ester represented by the general formula We claim:
1. A lubricating grease consisting essentially of a lubrieating oil thickened to a grease consistency with a compound having the general formula wherein A is chosen from the group consisting of acylacetarylamide, N-arylpyrazolone, and substituted acylacctarylamide and N-arylpyrazolone groups, and R and 7. The grease composition of claim 4 wherein the com- R' are chosen from the group consisting of hydrogen, position contains about 0.5-5 percent by weight of an methyl, methoxy and chlorine. amine oxidation inhibitor and about 1-10 percent by 2. The grease composition of claim 1 wherein the weight of an oil-soluble phosphorus acid ester. said lubricating oil comprises a silicone polymer oil hav- 8. A lubricating grease consisting essentially of a lubriing a viscosity in the lubricating oil viscosity range. eating oil thickened to a grease consistency with bis(acetyl- 3. The grease composition of claim 1 wherein the said N phenylcarbamylmethyl)4,4 disazo 3,3 diehlorodilubricating oil consists essentially of a methylphenyl siliphenyl. cone polymer having a viscosity in the range from about 9. A lubricating grease consisting essentially of a 300 to about 400 seconds SU at 100 F. methylphenyl silicone polymer having a viscosity of from 4. A lubricating grease consisting essentially of alubriabout 300 to about 400 seconds SU at 100' F. thickeating oil thickened to a grease consistency with a comened to a grease consistency by about 15-35% by weight pound having the formula based on the weight of the composition of bis(acetyl-N- wherein R is selected from the group consisting of aliphatic groups and aliphatic ether groups containing from 4 to 12 carbon atoms, R is an aliphatic group containing 10 from 1 to 12 carbon atoms, R, is an aliphatic group containing from 1 to 12 carbon atoms, and x is an integer from 1 to 5.
01130? R R mom wherein R and R are chosen from the group consisting phenylcarbamylmethyl)4,4' disazo 3,3 dichlorodiof hydrogen, methyl, methoxy and chlorine, and R" is phenyl. hydrogen or one or more lower alkyl groups.
5. The grease composition of claim 4 wherein the said lubricating oil comprises about -100 percent of a References Cited in the file of this patent UNITED STATES PATENTS methylphenyl silicone polymer oil having a viscosity in 1 932,577 Eichwedg 1 1 O t, 31, 1933 the range from about to about 900 seconds SU at 2,361,568 Reynolds Oct. 31, 1944 F. 2,604,469 Herrmann July 22, 1952 6. The grease composition of claim 4 wherein the said 40 2,791,560 Dilworth et al. May 7, 1957
Claims (1)
1. A LUBRICATING GREASE CONSISTING ESSENTIALLY OF A LUBRICATING OIL THICKENED TO A GREASE CONSISTENCY WITH A COMPOUND HAVING THE GENERAL FORMULA
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US631069A US2880177A (en) | 1956-12-28 | 1956-12-28 | Lubricating greases thickened with benzidine diazo compounds |
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US631069A US2880177A (en) | 1956-12-28 | 1956-12-28 | Lubricating greases thickened with benzidine diazo compounds |
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Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2978413A (en) * | 1958-12-19 | 1961-04-04 | Texaco Inc | Lubricating oils thickened to a grease consistency with cuprous n, n'-diarylamidine compounds |
US2984660A (en) * | 1958-05-23 | 1961-05-16 | Hoechst Ag | Disazo-dyestuff insoluble in water |
US3010905A (en) * | 1959-07-10 | 1961-11-28 | Texaco Inc | Lubricating greases thickened with nitrophenylazo naphthol compounds |
US3010904A (en) * | 1958-12-23 | 1961-11-28 | Texaco Inc | Lubricating greases thickened with dioxazine carbazole compounds |
US3013972A (en) * | 1959-08-06 | 1961-12-19 | Texaco Inc | Greases thickened with polyvalent metal salts of 2(2-hydroxy-3-carboxy-1-naphthylazo)benzenesulfonic acids |
US3025287A (en) * | 1960-04-08 | 1962-03-13 | Hoechst Ag | Disazo-dyestuffs insoluble in water |
US3030354A (en) * | 1959-03-04 | 1962-04-17 | Hoechst Ag | New disazo-dyestuffs insoluble in water |
US3102860A (en) * | 1960-08-31 | 1963-09-03 | Socony Mobil Oil Co Inc | Naphthalic imidazole grease |
US3226395A (en) * | 1960-10-04 | 1965-12-28 | Hoechst Ag | Water-insoluble phthalocyanine dyestuffs and process for their manufacture |
US3234133A (en) * | 1962-12-27 | 1966-02-08 | Texaco Inc | Grease composition |
US3235500A (en) * | 1962-12-27 | 1966-02-15 | Texaco Inc | Grease composition |
US3306890A (en) * | 1963-04-29 | 1967-02-28 | Allied Chem | Copper complexes of sulfamylphenylpyrazolone monoazo dyestuffs |
US3324106A (en) * | 1959-09-25 | 1967-06-06 | Kuhlmann Ets | 1-phenyl-5-pyrazolone-3-carbonamide disazo dyestuffs |
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US1932577A (en) * | 1931-12-24 | 1933-10-31 | Gen Aniline Works Inc | Water-insoluble disazo-dyestuffs |
US2361568A (en) * | 1942-02-25 | 1944-10-31 | Interchem Corp | Azo pigment |
US2604469A (en) * | 1947-12-30 | 1952-07-22 | Gen Aniline & Film Corp | Dustproofed organic color compounds |
US2791560A (en) * | 1954-04-14 | 1957-05-07 | Texas Co | Lubricating grease thickened with a sodium or lithium soap and indigo |
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- 1956-12-28 US US631069A patent/US2880177A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US1932577A (en) * | 1931-12-24 | 1933-10-31 | Gen Aniline Works Inc | Water-insoluble disazo-dyestuffs |
US2361568A (en) * | 1942-02-25 | 1944-10-31 | Interchem Corp | Azo pigment |
US2604469A (en) * | 1947-12-30 | 1952-07-22 | Gen Aniline & Film Corp | Dustproofed organic color compounds |
US2791560A (en) * | 1954-04-14 | 1957-05-07 | Texas Co | Lubricating grease thickened with a sodium or lithium soap and indigo |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2984660A (en) * | 1958-05-23 | 1961-05-16 | Hoechst Ag | Disazo-dyestuff insoluble in water |
US2978413A (en) * | 1958-12-19 | 1961-04-04 | Texaco Inc | Lubricating oils thickened to a grease consistency with cuprous n, n'-diarylamidine compounds |
US3010904A (en) * | 1958-12-23 | 1961-11-28 | Texaco Inc | Lubricating greases thickened with dioxazine carbazole compounds |
US3030354A (en) * | 1959-03-04 | 1962-04-17 | Hoechst Ag | New disazo-dyestuffs insoluble in water |
US3010905A (en) * | 1959-07-10 | 1961-11-28 | Texaco Inc | Lubricating greases thickened with nitrophenylazo naphthol compounds |
US3013972A (en) * | 1959-08-06 | 1961-12-19 | Texaco Inc | Greases thickened with polyvalent metal salts of 2(2-hydroxy-3-carboxy-1-naphthylazo)benzenesulfonic acids |
US3324106A (en) * | 1959-09-25 | 1967-06-06 | Kuhlmann Ets | 1-phenyl-5-pyrazolone-3-carbonamide disazo dyestuffs |
US3025287A (en) * | 1960-04-08 | 1962-03-13 | Hoechst Ag | Disazo-dyestuffs insoluble in water |
US3102860A (en) * | 1960-08-31 | 1963-09-03 | Socony Mobil Oil Co Inc | Naphthalic imidazole grease |
US3226395A (en) * | 1960-10-04 | 1965-12-28 | Hoechst Ag | Water-insoluble phthalocyanine dyestuffs and process for their manufacture |
US3234133A (en) * | 1962-12-27 | 1966-02-08 | Texaco Inc | Grease composition |
US3235500A (en) * | 1962-12-27 | 1966-02-15 | Texaco Inc | Grease composition |
US3306890A (en) * | 1963-04-29 | 1967-02-28 | Allied Chem | Copper complexes of sulfamylphenylpyrazolone monoazo dyestuffs |
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