US2380960A - Production of lubricants - Google Patents

Production of lubricants Download PDF

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US2380960A
US2380960A US449014A US44901442A US2380960A US 2380960 A US2380960 A US 2380960A US 449014 A US449014 A US 449014A US 44901442 A US44901442 A US 44901442A US 2380960 A US2380960 A US 2380960A
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soap
grease
aluminum
acid
hydrogenated
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US449014A
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Harold M Fraser
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INTERNAT LUBRICANT CORP
INTERNATIONAL LUBRICANT Corp
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INTERNAT LUBRICANT CORP
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M117/00Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof
    • C10M117/02Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof having only one carboxyl group bound to an acyclic carbon atom, cycloaliphatic carbon atom or hydrogen
    • C10M117/04Lubricating compositions characterised by the thickener being a non-macromolecular carboxylic acid or salt thereof having only one carboxyl group bound to an acyclic carbon atom, cycloaliphatic carbon atom or hydrogen containing hydroxy groups
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    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
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    • C10M2207/125Carboxylix 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
    • C10M2207/128Carboxylix 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 containing hydroxy groups; Ethers thereof
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    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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    • C10M2290/10Thickener
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    • C10N2010/00Metal present as such or in compounds
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
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    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Description

Patented Aug. 7, 1945 PRODUCTION OF LUBRICANTS Elan-old M. Fraser, New Orleans, La., assignor to international Lubricant Corporation, Orleans, La., a corporation oi. Lo
New
No Drawing. Application J one 29, 1942,
. Serial No. 449,014
Claims.
The present invention relates to the production of lubricants, and more particularly to lubricants containing a lubricant base as, for example, mineral oil or other equivalent oils well known in the art, and a material furnishing a hydrogenated ricinoleic acid radical: stated diflerently, a material containing the hydroxy fatty acid radicalof hydrogenated ricinoleic acid, said fatty acid radical being present in the lubricant, and particularly a grease in the form of a soap or a mixture of a soap and a fatty acid of hydrogenated casgor oil, otherwise termed l2-hydrozw-stearic aci In one form of the present-invention, it is desired to provide greases having incorporated indicates that it is the said hydroiw fatty acid radical which imparts the characteristic chemical and/or physical properties. to greases having present materials containing said radical.
Some of the materials, including those set forth furnishing l2-hydroxy-stearic acid or the hydroxy fatty acid radical of hydrogenated ricinoleic acid,.or what may be termed the hydrogenated ricinoleic acid, are soluble in the oil component of the lubricant grease, and therefore require no blending agent for their incorporation in the grease. As an example of such a material, there is set forth the lead soap of IZ-hydroxy-stearic acid, said soap being soluble in the mineral oil or other oil component of the grease. However, other materials containing the hydroxy fatty acid radical of hydrogenated riclnoleic acid are only slightly soluble or soluble with difllculty in mineral oils and other oils at low temperatures such as ordinary room temperatures, and therefore, it is necessary to provide for the permanent dispersion. or blending of such material including hydrogenated castor oil, IZ-hydroxy-stearicacid, and soaps of hydroxy stearic acid, including 12- hydroxy-stearic acid with the mineral and/or vegetable and/or animal oil constituent of the grease. In other words, when the material containing the hydroxy fatty acid radical of hydrogenated ricinolelc acid is soluble with dimculty, or only slightly soluble in a lubricant base,
1y disperse said material in the lubricant base. Examples of metal soaps only slightly soluble in the mineral oil base are the aluminum soaps of hydrogenated ricinoleic acid, and the aluminum, lead and sodium soaps of the polyhydroxy stearic acids. When the l2-hydroxy-stearic acid and/ or hydrogenated castor oil itself is incorporated in the mineral oil base, it is also desirable that a blending agent be present, and particularly the blending agent-comprising the aluminum soaps of the higher saturated fatty acids such as aluminum stearate, although other metal soaps may be used as the blending agent.
Many of the greases, particularly the soda base greases, when substantially dehydrated have a tendency to exhibit a granular structure. The metal soaps of hydrogenated ricinoleic acid, and particularly the metal soaps of hydrogenated castor oil as typified, bythe aluminum soap of hydrogenated ricinoleic acid, function as a granulation inhibitor, thereby producing a grease ofextremely smooth consistency. Similar results are obtained by incorporating in soda base greases varying amounts of hydrogenated castor oil itself or l2-hydroxy-stearic acid. These materials, as previously indicated, function similarly to the metal soaps of hydrogenated ricinoleic acid, since they are the full equivalents containing the essential hydroxy fatty acid radical of hydrogenated ricinoleic acid which is responsible for the granulation inhibiting property of said materials.
It is desired to point out it is highly advantageous to incorporate in greases soaps of hydroxy stearic acid, and particularly the lZ-hydroxy-stearic acid, because said soaps have a low water solubility. For example, the lead and aluminum soaps of hydrogenated castor oil or of 12- hydroxy stearic acid are substantially insoluble in water. The l2-hydroxy s'tearic acid itself and hydrogenated castor oil function similarly.
In accordance with the present invention, in one of its forms lubricant greases may have incorporated therein a soap of hydroxy-stearic acid, as for example a metal soap of said acids, and more particularly a metal soap of hydrogenated ricinoleic acid, said soap being the only soap. There may be a single soap of the above character present in the grease or a plurality of different soaps of the above character to thereby form a mixed soap base grease. For example, there may be present a mixture of the aluminum soaps and the lime soaps of the hydroxy-stearic acids, and particularly soaps of the 12-hydroxy-stearic acid, or the grease may have incorporated therein an aluminum soap, together with a sodium soa of a hydroxy-stearic acid of the character set forth. For example, there may be incorporated in the grease in addition to the lead soap of hydrogenatad ricinoleic acid an ordinary soda soap or a soda soap of hydrogenated ricinoleic acid. In short, the grease may have present a plurality of soaps, all of which may be soaps of hydroxystearic acidfor some of the soaps may be soaps of hydroxy-stearic acid, as for example metal soaps of hydrogenated ricinoleic acid, and the remaining soaps may be the ordinaryprior art soaps. The soaps present in the grease may be those of the monohydroxy-stearic acids, or those of the polyhydroxy-stearic acids, or the lubricant having said soaps present may also have any of the prior art soaps. Said soaps inherently contain because of their method of manufacture small quantities to relatively large quantities of 12-hydroxystearic acid. In the example herein set forth, there is always inherent present in the soap produced at least 3 to 6% of the free fatty acid of lwdrogenated castor oil, and consequently greases compounded in accordance with certain of the examples herein set forth do contain not only the soap of 12-hydroxy stearic acid but the 12-hydroxy-stearic acid itself, as will be more fully described hereinafter.
, In accordance with the present invention, certain addition agents maybe added to the grease to produce a smoother texture. Further, these greases function to reduce the milling time of the grease after cooling. It is preferred that these addition agents be added to pouring.
It is an object of the present invention to produce greases containing a material having present the hydroxy-fatty acid radical of hydrogenated ricinoleic acid, said radical being present. in a soap of hydrogenated ricinoleic acid, or in hydrogenated castor oil, or in 12-hydroxy-stearic acid itself, or in mixtures of any and all of said materials. While the l2-hydrorw-stearic acid may be obtained by saponifying an oil which has been hydrogenated, as for example castor oil, it is obvious that the 12-hydroxy-stearic acid may be produced by other methods. Soaps may be obtained from the lz-hydroxy-stearic acid by treating the latter with an organic compound or metal compound.
It is a further object of the present invention to incorporate in a grease in conjunction with a soap of polyhydroxy-stearic acid and/or a soap of 12-hydr'oxy-stearic acid, and/or 12-hydroxystearic acid itself, and/or hydrogenated castor oil, a metal salt of a higher unsaturated fatty acid, and particularly an aluminum salt of a higher saturated fatty acid, to produce greases novel in the art which possess the advantages above set forth, and other advantages which will appear from the following disclosure.
The present invention will be illustrated by a number of examples, the first of which will be directed to the incorporation of an aluminum soap of hydrogenated ricinoleic acid in the lubricant base, said soap requiring the presence of a dispersing or blending agent for the purpose of permanently blending and incorporating the soap in the lubricating base. 4
Referring to the blending agent, it may be stated that all of the aluminum soaps of the higher saturated fatty acids starting with those containing twelve (12) carbon atoms may be used as the carrier,-'dispers'ing or blending agent. The aluminum soaps of the unsaturated fatty acids carrying more than twelve (12) carbon atomsthe grease before a acid soaps adapted to be used as blending agents are:
Aluminum salt of palmitic acid. CuHnOa Aluminum salt of myristic acid CuHaO: Aluminum salt of lauric acid CuHaO: Aluminum salt of stearic acid Cal-Iss0:
Specific examples of suitable unsaturated fatty and resin acid soaps adapted to be used as blending agents are:
Aluminum salts of the following acids:
Myristolelc acid. CuHaOz Palmitoleic acid Cid-I300: Oleic acid CuHuO: Linoleic acid CuHnOz Linolenic acid CuHaoOs Abietic acid CmIhO:
the following characteristics: Titre 64.5 Sapon. No 178 Iodine N 2.5!
The hydrogenated castor oil is a solid and has a melting point of about 72 0., which indicates that the hydrogenation process has been practically carried to completion. The best results in practicing the present invention will be obtained by producing an aluminum soap of substantially completely hydrogenated csstor oil. However, the castor oil may be only partially hydrogenated and still may be used. Stated differently, the higher the degree of hydrogenation of the castor oil, the better results obtained when the aluminum soap thereof is incorporated in the lubricant base.
One thousand (1000) pounds of hydrogenated castor oil having the properties above set forth are mixed with two hundred and eighty (280) gallons of water and charged into a mechanically agitated kettle. This mixture is heated until the fatty material has melted. Thereafter, a solution of two hundred. and five (205) pounds of caustic soda dissolved in one hundred and seventy (170) gallons of water is run into the kettle slowly, the time consumed in said addition being approximately thirty (30) minutes. Heating and stirring is maintained for approxiately two (2) hours until the fatty base has saponifled. Thereafter. a solution of five hundred and sixty (580) pounds of aluminum sulphate dissolved'in two hundred (200) gallons of water which has been heated to approximately 1''. is run into the kettle, and the entire mixture agitated for a period of time suflicient to allow the aluminum salt to react with the water solution of the sodium hydrogenated ricinoieate, this usually taking, for
utes. The heating of the mixture is then stopped and the mixture is agitated until the aluminum soap has completely separated from the liquid. Thereafter, the liquid solution is drained from the bottom of the kettle. The soap remaining in the kettle is then washed by pumping therein water of the amount of about two hundred (200) gallons, the water being maintained at a temperature of from 150 to 175 F. After stirring for about ten (10) or fifteen m utes, t e tation is stopped and the wash Water is drained from the bottom of the kettle. Thisprocedure may be repeated until the aluminum soap of the hydrogenated castor oil is sufficiently pure for commercial purposes. the washing is repeated three (3) times.
This white insoluble soap of hydrogenated ricinoleic acid or soap of l2-hydroxy-stearic acid also contains at least 3 to 6% of the free fatty acid of hydrogenated castor oil or, stated diflerently, said soap contains in admixture therewith at least 3 to 6% of 12-hydroxy-stearic acid and in many cases a considerabl greater percentage is present. Therefore, greases or lubricants having incorporated therein soaps of lZ-hydroxy-stearic acid also carry varying amounts of l2-hydroxystearic acid, and since greases may be produced in accordance withthe present disclosure carrying up to 50% of soaps of 12-hydroxy-stearic acid, said greases inherently carry not only small, amounts of 12-hydroxy-stearic acid, but in some cases relatively large amounts of IZ-hydroxystearic acid. Therefore, in the above example the aluminum soap of 12-hydroxy-stearic acid carries at least 3 to 6% of 12-hydroxy-stearic acid.
set forth is added to the grease as set forth in Table II, then the amount of l2-hydroxy-stearic acid which will be present will vary between .015 to 03%. If in the composition set forth in Table II the amount of aluminum soap of hydrogenated castor oil is increased to 10% as it may well be, then the amount of lz-hydroxy-stearic acid present in the grease will vary from 0.3 to 0.6%. If 50% of the aluminum soap of 12-hydroxystearic acid is present in the composition set forth in Table II, then the amount of free 12- hydroxy-stearic acid will vary between 1.5 to 3%.
The aluminum salt of hydrogenated castor oil produced as above, contains a considerable quantity of water and, therefore, is pumped through a centrifuge where most of the water is removed. From the centrifuge, the moist aluminum salt of hydrogenated ricinoleic acid is removed to a hammer mill which breaks the salt into small granules. Preferably, the granules are' then placed on trays and introduced into ovens heated with hot air to a temperature of about 200 F. The aluminum salt of the hydrogenated castor oil is allowed to remain in the oven until it is dried, which is usually about twenty-four (24) hours. The dried salt is then run through a hammer mill adapted to break the salt into such a fine flocculent state that substantially all of the salt will pass through a one hundred (100) mesh sleve.
Instead of using aluminum sulphate, aluminum chloride may be used or any other water soluble aluminum salt, the acid radical of which will combine with the sodium to release the aluminum so that it may combine with the fatty acid, the sodium salt being water soluble.
Instead of treating hydrogenated castor oil as set forth, for a portion of the hydrogenated castor oil there may be substituted stearic acid or any Usually it is sufficient if If one-half percent of the soap produced as above material having present this constituent. The mixture of the hydrogenated castor oil and the stearic acid containing material may be treated as hereinbefore described in connection with bydrogenated castor oil. However, with the presence of the stearic acid component on the addi tion of a water soluble aluminum salt, aluminum stearate is formed in addition to the aluminum soap of hydrogenated ricinoleic acid or castor oil. In general, the hydrogenated ricinoleic acid may have substituted therefor up to fifty per cent (50%) of a stearic acid'component. For example, instead of treating one thousand pounds (1000 lbs.) of hydrogenated castor oil, there may be substituted for this constituent a mixture of nine hundred pounds (900 lbs.) of hydrogenated castor oil and one hundred pounds lbs.) of a material containing stearic acid; or the mixture may contain twenty per cent (20%), thirty per cent (30%), forty per cent (40%), Or fifty per cent (50%) of a stearic acid component or any other intermediate per cent, as for example twenty-five per cent (25%), thirty-five per cent (35%), or forty-five per cent (45%). The amount of stearic acid material which is substituted for a portion of the hydrogenated castor oil will vary in accordance with the desired characteristics of the final lubricating grease and the use for which it is intended.
It is desired to point out that the presence of the stearic acid component in the mixture of hydrogenated castor oil and stearic acid facilitates the cooking operation, that is, the melting of the fatty material, and further, produces a product which can be Washed and centrifuged with greater case than the aluminum soap of hydrogenated castor oil itself. This is a decided advantage.
The aluminum salt of hydrogenated ricinoleic acid containing because of its method of production a small quantityof 12-hydroxystearic acid or hydrogenated castor oil, together with a metal salt of a saturated or unsaturated fatty acid and particularly aluminum stearate or other aluminum or fatty acid soap, may be introduced into a lubricant base in any proportion, and particularly in such proportions as ar herein pointed out which function to prevent oil seepage or bleeding and also function to improve the' texture of the resulting lubricant, that is, which will prevent the granulation of the lubricant, reduce the graininess of the lubricant, and in general make the resultin lubricating grease smoother and firmer than would have been the case had the material containing the 12-hydroxy stearic acid radical been omitted.
While it is not desired to be limited to a lubrieating base or a grease containing any particular percentage of a material containing a soap of 12-hydroxy-stearic acid or lZ-hydroxy-stearic acid itself, or hydrogenated castor oil, in general it may be stated that the lubricant base may have said materials including the soaps present in amounts up to 50% of the total weight of the grease. In the more limited aspect of th present invention,-the aluminum salt of hydrogenated ricinoleic acid, and particularly castor oil, hydrogenated castor oil, and 12-hydroxy-stearic acid may be present in the lubricant or grease in amounts varying between A to 10% based on the total weight of the lubricating grease, the latter preferably having present other soaps such as ordinary aluminum soaps, sodium soaps, or the like. Satisfactory results have been obtained when th aluminum salt of hydrogenated ricinoleic acid or aluminum salt of lZ-hydroxy-stearic acid is present in amounts ranging from to 5% based on the total weight of the lubricating grease. Similar percentages of 12-hydroxystearic acid or hydrogenated castor oil may also be used, preferably in combination with the metal soaps of the saturated fatty acids such as aluminum stearate. It may be pointed out that the solid or semi-solid lubricants 0f the present invention having incorporated therein aluminum soaps 0f hydrogenated ricinoleic acid, and especially hydrogenated castor oil and/or the equivalents thereof, as above pointed out, together with other soaps such as aluminum stearate or sodium soaps, have more desirable properties than would have been the case had the same lubricant been used without the addition of the herein set forth aluminum soap of hydrogenated ricinoleic acid, and preferably the aluminum soap of hydrogenated castor oil Or their equivalents, as above pointed out. As pointed out, instead of using the aluminum soap of hydrogenated castor oil, a mixture of the soap and aluminum stearate or other metal fatty acids, especially the metal soaps of the higher saturated and unsaturated fatty acids containing twelve (12) carbon atoms or more, the latter functioning as a carrier dispersing or blending agent, may be incorporated in a grease or semi-solid lubricant. When the mixture is incorporated in the lubricant or grease usually more of the mixture is used than when the aluminum soap of hydrogenated castor oil is introduced by itself into the grease. For example, when one-quarter A) of one (1) per cent of the aluminum soap of the hydrogenated castor oil is added to the lubricating grease to produce the desired result, if a fifty-fifty mixture of the said soap and an aluminum stearate is used onehalf per cent of the mixture will be added to the lubricant to produce the same or similar result.
The advantages residing in the present invention will be clear from the following: a regular aluminum stearate grease was made up according to the following formula:
Table! Per cent Aluminum stearate 175 vis. oil at 100 F, (mixed base paraffin and asphalt oil) 93 Table II Per cent Aluminum stearate 6 Aluminum soap of hydrogenated castor oil /2 175 vis. oil at 100 F. (mixed base paraffin and asphalt oil) 93 The lubricant produced in accordance with the mixture of Table II stood for several days without any oil seeping therefrom. This indicates the advantage of having present the aluminum soap of hydrogenated castor oil. The A. S. T. M. worked penetration on the above grease was 346.
tion of a small amount of the aluminum soap of hydrogenated ricinoleic acid, and particularly other soaps, and especially those containing aluminum soaps, that the resulting grease is more stable, and smoother, and firmer, than a grease of similar characteristics, but in which no aluminum soap of hydrogenated castor oil is present.
Further, as pointed out, when agents are added in small quantities to make the grease harder, as for example, rosin, rosin oil, the resulting grease. despite the addition of the hardening agent, is still smooth and firm and does not leak oil, provided there has been incorporated in the grease a small amount of an aluminum soap of hydrogenated ricinoleic acid, or of hydrogenated ricinoleic acid, or 12-hydroxy stearic acid, the soap or equivalent being present in amounts varying from one-quarter A) to ten per cent (10%) and preferably one-quarter to five per cent (5%). The aluminum soap of hydrogenated ricinoleic acid orequivalent may be present in some cases in greater amounts up to fifty per cent (50%) of the total weight of the rease.
It is also desired to point out that those greases having the granulation inhibitor of the present invention, after being mixed, are poured into pans of any suitable size, as for example, twentyfour by sixty inches (24 x 60), the depth of the grease layer being about three inches (3"), and r then cooled by blowing first with warm air having a temperature of 125 F, and then slowly reducing the temperature of the air to room temperature over a period of eight (8) to twelve (12) hours.
It may be pointed out that it is a general rule that the hardness of the grease may be increased by increasing the amount of soap present. In other words, if the grease of Table II has the aluminum stearate increased from six and one-half per cent (S to eight (8%) the resulting grease would have a harder consistency than a grease having merely six and one-half per cent of the aluminum stearate.
The aluminum soap of hydrogenated ricinoleic acid and especially castor oil may be incorporated in a soda soap grease in accordance with the following:
Per cent Sodium soap of hydrogenated fish fatty acids having a titre of 51 to 56 2.5 Sodium soap of hydrogenated fish fatty glycerides 1.0 Sodium soap of regular castor oiL .25 Sodium soap of hydrogenated castor oil 25 Sodium soap of rosin .2 Aluminum soap of hydrogenated castor oil- .3 Aluminum stearate .2 coastal oil 15.0 3600 Green cast red coastal oil 79.65
It is desired to point out that in the above composition the soap content may be varied to suit the type of lubrication required. In said composition the amount of the sodium soaps may be materially increased and moreover, the amount aaeopoo of aluminum soap of hydrogenated castor oil may be increased. It may vary, as pointed out, from one-quarter 4%) per cent'to ten per cent or even, in some circumstances, less than one-quarter, (14%) of one per cent (1%), this however being unusual. Instead of using in the above composition aluminum stearate as the carrier dispersing or blending agent other aluminum soaps' of the higher fatty acids may be used as herein previously disclosed. However, the aluminum stearate gives the preferred results. The amount of blending agent used may vary over a very considerable range depending upon the character of the lubricating grease being treated.
In preparing the above, the sodium soaps and the Coastal Pale are heated ina vessel to which is then added .3 of 1% of the aluminum soap of hydrogenated castor oil and .2 of 1% of aluminum stearate. The heating is then continued until the grease melts to a sticky mass. upon, additional oil, that is, the 3600 green cast red oil is added slowly while stirring, the mixture being brought to a temperature of about 350 to 410 F. The grease is then pumped or poured at a temperature of about 350 to 360 F. into pans of any suitable size, the depth of the grease layer being about three (3) to four (4) inches. The grease is then cooled in a manner similar to that pointed out in connection with previous examples. The grease prepared in accordance with the above had an ASTM worked penetration of about 310 to 325 and the grease had a melting point of 300? F. The grease did not leak oil and was exceedingly stable during storage. In the grease prepared without the aluminum salt of hydrogenated castor oil, there would have been some leakage, and during storage, the grease would not have been as stable. This indicates the advantages of the present invention.
Further, it is desired to point out that if the aluminum soap of hydrogenated castor oil was omitted, the grease did not gel properly and the oil separated from the soap base.
Instead of incorporating the aluminum stearate in the grease in the manner above set forth, the grease may be prepared with the aluminum soap of hydrogenated castor oil, and another grease may be prepared with the aluminum stearate. When the two greases have been poured and cooled they may be then milled together as set forth in Fraser Patent No. 2,257,945.
It is desired to point out that the grease is poured at about 350 to 360 F., and the grease is cooled from this temperature to approximately 100 F. in twelve (12) hours to thereby produce a transparent grease, the water content of which is less than A; of 1%).
The aluminum soaps of hydroxy-stearic acid, and particularly the aluminum soap of 12-hydroxy-stearic acid, this soap being produced by various means, but preferably by saponification of hydrogenated ricinoleic acid, is not readilyaluminum soap of hydrogenated ricinoleic acid is substantially permanent.
If the aluminum soaps of non-hydrogenated commercial castor oil are used to replacethealuminum soap of the hydrogenated castor oil in Therethe above compounds, the resulting grease is much softer and the oil seeps out. It may be stated that in general, greases made with the addition-of the aluminum soap of hydrogenated ricinoleic acid, and especially hydrogenated castor oil, said greases containing other soaps of the fatty acids, soaps of rosin, and the like, are similar in body, exceedingly stable relative to oil separation, and retain their consistency better when worked than greases of substantially the same composition, but in which there is no aluminum soap of the hydrogenated ricinoleic acid, or more specifically the aluminum soap of hydrogenated castor oil.
It may be pointed out that the hydrogenated ricinoleic acid of the 12-hydroxy-stearic acid has an OH group present in the chain, and this is not true of the other fatty acids. It is believed that the manner in which the aluminum salt of hydrogenated ricinoleic acid acts in the present invention to prevent granulation and seepage of oil is due to the presence of an OH group in the chain. This same hydroxy fatty acid group is present in 12-hydroxy stearic acid and in hydrogenalted castor oil, and these materials when incorporated in a lubricant would impart the same characteristic chemical and physical properties to said lubricant as when the soaps of v12- hydroxy-stearic acid are incorporated in the lubricant. As pointed out, the essential structural feature of all of these compounds is the presence of the hydroxy-fatty acid radical of hydrogenated ricinoleic acid, and therefore the compounds are full equivalents and the soaps when produced in accordance with the method herein set forth contain in some cases small amounts and in other cases relative large amounts of 12- hydroxy stearic acid itself. From the above, it can be gathered that the aluminum soaps of the other fatty acids are not the equivalent of the aluminum soaps of hydrogenated ricinoleic acid as derived from hydrogenated castor oil.
While it is clear that the amount of carrier or blender may greatly vary, in general there should be about one-quarter A) or one-half to fifteen (15) parts of blending agent for every part of aluminum salt of hydrogenated castor oil or for every part of 12-hydroxy-stearic acid or hydrogenated castor oil. In some cases the amount of blending agent may be in the ratio of three (3) 'to thirty (30) parts of the blending agent to one (1) part of the material containing the hydroxy fatty acid radical of hydrogenated ricinoleic acid as typified by the aluminum soap of hydrogenated castor oil, or
' said soap containing a small amount of 12-hydroxy-stearic acid, or 12-hydroxy-stearic acid itself, or hydrogenated castor oil.
In accordance with the present invention, lead soaps of hydrogenated ricinoleic acid may also be incorporated in grease made from a. mineral, animal or vegetable base, or a combination of the same. The incorporation of the lead soaps of hydrogenated ricinoleic acid produces a grease which has'a good body, even in the presence of only a small percentage of the lead soap. The grease containing the lead soap of ricinoleic acid is characterized by hardness, a high melting point even in the presence of a small percentage of soap, insolubility in water, and a high film strength, as compared to other greases, including those greases containing the ordinary lead soap of castor oil. The lead soap of hydrogenated ricinoleic acid is soluble in the usual lubricant bases, as for example mineral oils, in proportion up to 40 to 50%. Usually, it is only necessary to incorporate in the grease a small percentage of this soap, as for example /2 to 2%, with the result that there is produced, even with this low soap content, a grease that has a high melting point and is characterized by water insolubility. While it has been stated that the lubricant grease shouldonly contain a small percentage of the lead soap of hydrogenated ricinoleic acid, that is from about A to 4%., greases containing up to 50% of this soap which are hard greases may be used as block greases on railroad axles, colander bearings, and for other purposes where it is known that a hard grease is necessary or desirable.
The following table sets forth greases containing 1%, 2% and 4% of the lead soap of hydrogenated ricinoleic acid, together with the worked penetration and the melting point of the result ing greases:
Table III A. S. T. M. Ubbelohde worked penemelting nation point 4 lead soa of h drogenated ricinoleic F.
3c H 250 25s lead son of h dro enate ricinoleic 3a 317 250 1% lead soap of hydrogenated ricinoleic acid 348 249 Mixed soap base greases containing the lead soap of hydrogenated ricinoleic acid, together with other soaps, were prepared by taking a grease containing 2% of the lead soap of hydrogenated ricinoleic acid, as for example the lead soap of hydrogenated castor oil, and mixing therewith a soda base grease containing 4% of a soda soap. These greases were mixed when cold in various proportions. 75% of the grease containing the lead soap of hydrogenated ricinoleic acid was mixed with 25% of the soda soap grease and the grease had a Ubbelohde melting point of 255 F. The final mixed base grease carried a total soap content of 2 of which l /2% was the lead soap of hydrogenated castor oil and 1% was the ordinary soda soap. In place of the ordinary soda soap there may be substituted a soda soap of hydrogenated castor oil.
Another grease was prepared by mixing 62 of the grease containing 2% of the lead soap of hydrogenated ricinoleic acid with 37%% of the grease containing 4% of a soda soap. The final grease which has a Ubbelohde melting point of 300 F. and carried approximately 3% total soap content, has incorporated therein approximately 1% of a lead soap and approximately 2% of the soda soap.
Another grease was made by mixing 25% of the grease containing 2% of the lead soap of hydrogenated castor oil and 75% of the grease containing 4% of the soda soap. The resulting grease which carried 3 total soap content and had a Ubbelohde melting point of 205 F. carried /2% of the lead soap and 3% of the soda soap.
The above greases were smooth, transparent and of good appearance. If the above mixture of greases are heated above the melting point and cooled, the heat treated greases are much softer and grainier than if the greases are mixed cold, and in view of the above, it is desired that the greases be mixed in a cold state, although heat may be employed under some circumstances.
Another mixed base soap grease was made by .in the cold to provide a smooth, transparent grease of good appearance.
Another mixed soapbase grease was prepared by mixing in the cold 50% of a grease containing 2% of the lead soap of hydrogenated castor oil with 50% of a lime ,base grease containing 10% of a lime soap. The resulting grease containing 1% of the lead soap of hydrogenated castor oil and 5% of a lime oap of fatty acids, had a melting. point of 205 F. The mixed grease was smooth, translucent and of good appearance. Another grease was made by mixing together equal parts of a grease containing /2% of a lead soap of hydrogenated castor oil and a soda base grease containing 10%% of soda soap. The resulting grease was melted together and poured into a pan at 250 F.. It was then cooled and found to have a melting point of 356 F. and an A. S. T. M. worked penetration of 240. The grease contained a total soap content of 11%, of which was a lead soap, and the remainder was the soda soap. The free alkali content of the resulting grease, as determined by the regular A. S. T. M. method was .08%, and the grease had a Saybolt oil viscosity of 500 seconds at F. When rolled in ball bearings, it retained the same approximate consistency for a working time of two hours.
Greases may be prepared containing the alkali earth soaps of hydrogenated ricinoleic acid such as castor oil. More specifically, there may be dissolved and incorporated in the mineral oil 1 to 8% of calcium soap of hydrogenated castor oil; or 1 t0 8% of the strontium soap of hydrogenated castor oil; or 1 to 8% of the barium soap of hydrogenated castor oil. These soaps are dissolved and incorporated in the mineral oil at a temperature of 350, and on cooling the soap separated from the oil. However, if the grease is reheated at a suitable temperature, as for example 220, and there is added an agent adapted to cause an emulsion to form, as for example about 1% of water based on the weight of the grease, an emulsion is formed and solid greases are obtained on at room temperature in 8 to 10 hours. The grease containing the nickel soap of hydrogenated ricinoleic acid, as for example castor oil, yielded a soft gel, but the other greases were of a more fluid viscous consistency. These greases of a fluid consistency exhibited properties which make them adaptable for many lubricating purposes.
While the present invention in its preferred form is directed to the production of greases in a solid form and desirably havin a low soap content with a high melting point, the invention is not limited thereto and includes the production (Ti liquid lubricating mediums, including fluid viscous lubricants adaptable for use in connection with the lubrication of Diesel engines. Such fluid lubricants may also be used as transmission oils, motor oils, and the like.
. While it has beenspecified that the soap of hydrogenated castor oil which is used is the metal soap, it is within the province of the present invention, in some cases, to substitute for the metal base an organic radical to produce an organic soap. For example, instead of using a metal constituent, the hydrogenated fatty acid may be combined with ethanolamlne to produce an amine soap which when incorporated in the lubricating greases, especially the fluid viscous lubricants, gives desirable results.
The soda soap of hydrogenated ricinoleic acid, as for example castor oil, may be formed directly in a mineral oil such as was used for the produc tion of the soaps immediately above described, said oil having a 300 viscosity at 100 Saybolt.
The sodium soap oi hydrogenated castor oil may be made by the direct saponification of hydrogenated castor oil present in the mineral oil. After the saponifying caustic soda 'has been added,
the temperature is raised to 350 F., and the mixture heated during saponification to drive off substantially all of the moisture. The resulting grease is smooth, pliable and has a worked A. S. T. M. consistency of 350 to 375 and contains 8% of sodium soap.
While in the majority of cases the herein described soaps may be dispersed in a mineral oil base, it is obvious that the mineral oil base mayhave mixed therewith any of the well known lubricating bases including hydrogenated fish oil, animal oils, vegetable oils, and rosin or a plurality thereof.
As previously pointed out, the soap which is incorporated in the grease in accordance with the present invention may in one form of the invention be a soap of hydrogenated ricinoleic acid which, as stated. may be termed a l2-hydroxystearic acid. This designation, in accordance with the common usage, means that the hydroxy group is on the twelfth carbon atom from the carboxyl group.
In accordance with the present invention, the
lubricating medium as, for example, a grease, may
have incorporated therein a soap of a 10-hydroxystearic acid, as for example the lead soap of this acid. Thisproduct may be manufactured by several accepted methods of preparation, including a metathesis reaction utilizing a soluble lead salt such as lead acetate in reaction with the sodium soap of the lO-hydroxy-stearic acid. The lead soap of the IO-hydroxy-stearic acid has a somewhat soften texture and a lower solubility in the mineral oil bases in which the lead soap of the 12-hydroxy-stearic acid was incorporated. Further, the lead soap of the 10-hydroxy-stearic acid does not gel and/or harden the grease in which is incorporated to the same optimum degree as that which occurs when the lead soap of the 12-hydroxy-stearic acid, the acid of which has been produced by acid or by other means, is incorporated in the grease.
In accordance with the present invention there may also be incorporated in a lubricating medium soaps of the poly-hydroxy-stearicacids. For ex- The , droxy stearic acid, said soap being produced by the metathesis or double decomposition method. The sodium soap produced, as above set forth,
was only slightly soluble in the mineral oil base and was soluble even with difficulty at 400 F; Therefore, it is necessary when incorporating this product to provide for a carrier much in the same manner as when the aluminum soap of ricinoleic acid is incorporated in a lubricant base.
The aluminum soap of the 9 and 10 dihydroxystearic acid also was slightly soluble in the hydrocarbon oil, preferably at temperatures approximating 400" F.
The lead soap of this dihydroxy-stearic acid, the hydroxy groups being in the 9 and 10 position, was prepared by the methods above set forth, and its properties were substantially parallel to that of the sodium and aluminum soap above set forth, except that it was more soluble in the hydrocarbon base and the solubility was better at 300 F. On heating to a higher temperature there was some degradation of the lead soap which re- .sulted in a grease which on cooling possessed the characteristics of a grease showin a low solubilized content of lead soap.
From the above it appears that the presence of more than one hydroxy group in a hydroxystearic acid soap reduces the solubility of metal soaps thereof in the lubricant base. Because of this reduced solubility, these soaps should preferably be added to the lubricant base in amounts under 1%,,although when a carrier is used the amounts'may be increased. However, it is desired to point out that the soaps of the polyhydroxystearic acids, as a class, exhibit inferior jellying characteristics as far as their effects upon the mineral oil base is concerned.
, It is desired to point out that irrespective of whether the lubricating medium is a grease or a viscous non-solid lubricat ng medium, it may have incorporated therein a mixture of a metal soap of a mono or polyhydroxy-stearic acid, to-
gether with an organic soap of a mono or polyhydroxy-stearic acid. In other words, instead of having a metal coupled to the acid constituent, the hydroxy-stearicacid may have coupled thereto an organic base. In the more specific aspect of the invention, the metal soap of the l2hydroxy-stearic acid which is herein termed the metal soap of hydrogenated ricinoleic acid, may have mixed therewith an organic soap of the 12- hydroxy-stearic acid.
, In general it may be stated that in the lubrieating medium herein disclosed, all or part of the metal soap of any of the hydroxy-stearic acids herein set forth may have all or part of the metal soap substituted by a soap made by sapon fying a hydroxy-stearic acid with an organic base to produce what may be termed an organic soap.
Referring to the preparation of greases which contain the aluminum soaps of hydrogenated ricinoleic acid, together with a carrier for the same,
.the aluminum soap of the hydrogenated ricinoleic acid is greatly improved due to the fact that one or more of the bonds of the aluminum contains or is coupled up with stearic acid, while the other bond is coupled up or contains hydrogenated ricinoleic acid.
It is desired to point out that in. general the lubricants, including the greases, mayhave present an organic soap of any of the hydroxy-stearic acids, including the mono-hydroxy-stearic acid and the polyhydroxy-stearic acids, and more specifically any of the herein mentioned metallic metal soaps, including aluminum, sodium, barium,
lead, strontium, calcium, magnesium, tin, nickel, cobalt, chromium, manganese, and the like, or
the lubricant including greases may have incorporated therein a plurality of any of the herein described soaps to thereby produce a mixed base lubricant.
The following illustrates the production of greases using an aluminum stearate grease which did not have incorporated therein a soap of 12- hydroxy-stearic acid or other equivalents, hydrogenated castor oil, or 12-hydroxy-stearic acid itself, and greases in which in one case there is incorporated hydrogenated oastor oil, and in anothe case 12-hydroxy-stearic acid. In one case a mixture was made of 6.8% aluminum stearate and 93.2% of a mixed parafiin and asphalt base oil having 180 Saybolt viscosity at 100 F. The resulting grease had an AS'IM worked penetration of 298 and was characterized by graininess and substantial seepage of oil.
Another lubricant was compounded having 6.8% aluminum stearate, 92.7% of the same oil base, and .5% of hydrogenated castor oil. The resulting grease had a worked penetration of 331. The grease instead of being grainy was smooth and showed substantially no oil separation. An-
other grease was compounded, using 6.8% of aluminum stearate, 92.7% of the same oil base, and .5% of free fatty acid of hydrogenated castor oil, or 12-hydroxy-stearic acid. The resulting grease was transparent and had an ASTM worked penetration of 334. The resulting grease was smooth and showed no oil separation.
Instead of using an aluminum stearate in the above examples, other aluminum salts of saturated and unsaturated fatty acids may be used.
This application is a continuation-in-part, of
application Serial No. 347,533, filed July 25, 1940, said application being a continuation-impart of application Serial No. 268,781, filed April 19, 1939.
I claim:
1. A lubricating grease containing a lubricant base together with a soap of a 12-hydroxy-stearic acid together with a blending agent therefor.
2. A lubricating grease containing a lubricant base together with a metal soap of a 12'-hydroxystearic acid together with a blending agent therefor.
3. A lubricating grease containing a lubricant base together with' a soap of 12-hydroxy-stearic acid.
4. A lubricating grease containing a lubricant base together with a metal soap oi. 12-hydroxystearic acid.
5. A lubricating grease containing a lubricant base together with a soap of hydrogenated ricinoleic acid.
6. A lubricating grease containing a lubricant base together with l to 10% of a soap of hydrogenated ricinoleic acid.
'7. A lubricating grease containing a lubricant base together with a metal soap of hydrogenated ricinolelc acid.
8. A lubricating grease containing a lubricant base together with 1 to 10% of a metal soap of hydrogenated ricinoleic acid.
9. A lubricating grease containing a lubricant base and having dispersed therethrough a metal soap of hydrogenated ricinoleic acid together with a blending agent therefor.
10. A lubricating grease containing a lubricant base, said grease having its normal texture modifled by the presence of a metal soap of hydrogenated ricinoleic acid acting as a granulation inhibitor.
11. A lubricating grease containing a lubricant base together with an aluminum soap of hydrogenated ricinoleic acid in an amount adapted to inhibit granulation of the grease.
12. A lubricating grease containing a lubricant base together with an aluminum soap of 12-hy droxy-stearic acid in an amount adapted to inhibit granulation of the grease, and a carrier for said granulation inhibitor.
13. A lubricating grease containing a lubricant base together with an aluminum soap of hydrogenated ricinoleic acid in an amount adapted to inhibit granulation of the grease, and a metal soap of a fatty acid having at least twelve carbon atoms, said metal soap functioning as a carrier and blending medium for said granulation inhibitor.
14. A lubricating grease containing a lubricant base together with an aluminum soap of hydrogenated ricinoleic acid in an amount adapted to inhibit granulation of the grease, and an alu minum soap of a 'fatty acid having at least twelve carbon atoms, said aluminum soap functioning as a carrier and blending medium for said granulation inhibitor.
15. A lubricating grease containing a lubricant base together with from to 10% of an aluminum soap of hydrogenated ricinoleic acid, and a metal soap of a fatty acid having at least twelve carbon atoms functioning as a carrier and blending agent for said aluminum soap.
16. A lubricating grease containing a lubricant base together with from A% to 10% of an aluminum soap of hydrogenated ricinoleic acid, and an aluminum soap of a fatty acid having at least twelve carbon atoms, the latter functioning as a carrier and blending agent for said aluminum soap of hydrogenated ricinoleic acid.
17. A lubricating grease containing a lubricant base together with to 5% of an aluminum soap of hydrogenated ricinoleic acid and a carrier adapted to permanently disperse and incorporate the aluminum soap in the lubricating grease, the carrier being present in the ratio of three to thirty parts to one part ,of said aluminum soap.
18. An aluminum base grease having incorporated therein /2% to 5% of the aluminum soap 'of hydrogenated ricinoleic acid.
19. An aluminum base grease having incorporated therein aluminum stearate and from A to 5% of the aluminum soap of hydrogenated ricinoleic acid.
20. A soda base grease having incorporated therein to 5% of an aluminum soap of 12- hydroxy-stearic acid.
21. A soda base grease having incorporated therein sodium soaps of fatty acids, sodium rosinate, and a small percentageof an aluminum soap of 12-hydroxy-stearic'acid, the latter functioning to stabilize the grease and prevent oil leakage.
22. A soda base grease having incorporated therein fatty acid soaps, sodium soaps, a hardening agent, a small percentage of an aluminum soap oi'hydrogenated ricinoleic acid, the latter functioning to stabilize the grease and prevent oil leakage,and a carrier and blending agent for said aluminum soap.
23. A soda base grease having incorporated therein about four percent (4%) of fatty acid sodium soap, less than one per cent (1%) of a hardening agent, less than one per cent (1%) of an aluminum soap of hydrogenated ricinoleic acid, the latter functioning to stabilize the grease and prevent oil leakage, and less than one per cent (1%) of a carrier and blending agent for said aluminum soap.
24. A soda base grease having incorporated therein up to four per cent (4%) or fatty acid sodium soap, a hardening agent, one-quarter (V4%) to five per cent (5%) of an aluminum soap of hydrogenated ricinoleic acid, the latter functioning to stabilize the grease and prevent all leakage, and a carrier and blending agent for said aluminum soap, the former being present in the ratio of V to parts to one part of the aluminum soap.
25. A lubricating grease containing a lubricant base and an in situ-tormed mixture of an aluminum soap of hydrogenated ricin'oleic acidand a'blending agent for said aluminum soap.
-26. The method comprising inhibiting granu- J lation of a lubricating grease by adding thereto a small proportion of an aluminum soap of hydrogenated ricinoleic acid.
27. The method comprising inhibiting granulation of 'a lubricating grease by adding thereto a small proportion of an aluminum soap of hydrogenated ricinoleic acid together with a carrier for said soap capable of permanently dispersing said soap in the lubricant base. 28. The method of forming a lubricating grease comprising mixing an alkaline earth metal base soap or lz-hydroxy-stearic acid with an oil base, heating the resulting mixture in the presence of water adapted to produce an emulsion, and cooling whereby a solid grease containing said soap is produced.
29. In the production of greases containing an 011 base and soaps, the step of cooking together the oil base, an aluminum soap of a fatty acid and an aluminum soap of 12-hydroxy-stearic acid whereby the disperslbility of the resulting soap in the grease is greatly improved.
30. -In the production of greases containing an oil base and soaps, the step 01' cooking together the oil base, an aluminum soap of a stearic acid and an aluminum soap of lz-hydroxy-stearic acid whereby the dispersibility of the resulting soap in the grease is greatly improved.
mom M.
US449014A 1940-01-09 1942-06-29 Production of lubricants Expired - Lifetime US2380960A (en)

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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2445936A (en) * 1945-04-27 1948-07-27 Shell Dev Waterproofing of lubricating greases
US2448721A (en) * 1942-08-14 1948-09-07 Nopco Chem Co Aluminum soap greases
US2450222A (en) * 1945-09-07 1948-09-28 Texas Co Shear-resistant greases
US2450255A (en) * 1945-04-17 1948-09-28 Texas Co Method of preparing lithium base greases
US2455649A (en) * 1944-08-29 1948-12-07 Standard Oil Dev Co Solidified oils and methods of manufacture
US2503749A (en) * 1945-02-28 1950-04-11 Texas Co Barium soap grease compositions and method of preparation
US2607734A (en) * 1950-05-20 1952-08-19 Standard Oil Dev Co Process of manufacturing hydroxy acid greases and product thereof
US2607735A (en) * 1949-03-12 1952-08-19 Standard Oil Dev Co Alkaline earth metal soap greases
US2608493A (en) * 1948-06-30 1952-08-26 Nopco Chem Co Synthetic waxes
US2613182A (en) * 1950-01-05 1952-10-07 Standard Oil Dev Co Keto-acid soap greases
US2841557A (en) * 1956-01-24 1958-07-01 Sinclair Refining Co Lithium soap grease and process of making same
US11760952B2 (en) 2021-01-12 2023-09-19 Ingevity South Carolina, Llc Lubricant thickener systems from modified tall oil fatty acids, lubricating compositions, and associated methods

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2448721A (en) * 1942-08-14 1948-09-07 Nopco Chem Co Aluminum soap greases
US2455649A (en) * 1944-08-29 1948-12-07 Standard Oil Dev Co Solidified oils and methods of manufacture
US2503749A (en) * 1945-02-28 1950-04-11 Texas Co Barium soap grease compositions and method of preparation
US2450255A (en) * 1945-04-17 1948-09-28 Texas Co Method of preparing lithium base greases
US2445936A (en) * 1945-04-27 1948-07-27 Shell Dev Waterproofing of lubricating greases
US2450222A (en) * 1945-09-07 1948-09-28 Texas Co Shear-resistant greases
US2608493A (en) * 1948-06-30 1952-08-26 Nopco Chem Co Synthetic waxes
US2607735A (en) * 1949-03-12 1952-08-19 Standard Oil Dev Co Alkaline earth metal soap greases
US2613182A (en) * 1950-01-05 1952-10-07 Standard Oil Dev Co Keto-acid soap greases
US2607734A (en) * 1950-05-20 1952-08-19 Standard Oil Dev Co Process of manufacturing hydroxy acid greases and product thereof
US2841557A (en) * 1956-01-24 1958-07-01 Sinclair Refining Co Lithium soap grease and process of making same
US11760952B2 (en) 2021-01-12 2023-09-19 Ingevity South Carolina, Llc Lubricant thickener systems from modified tall oil fatty acids, lubricating compositions, and associated methods

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