US3857789A - Slushing oil or rust inhibiting compositions - Google Patents
Slushing oil or rust inhibiting compositions Download PDFInfo
- Publication number
- US3857789A US3857789A US00084540A US8454070A US3857789A US 3857789 A US3857789 A US 3857789A US 00084540 A US00084540 A US 00084540A US 8454070 A US8454070 A US 8454070A US 3857789 A US3857789 A US 3857789A
- Authority
- US
- United States
- Prior art keywords
- percent
- composition
- weight
- acid
- sulfonate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/022—Well-defined aliphatic compounds saturated
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/024—Well-defined aliphatic compounds unsaturated
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/04—Well-defined cycloaliphatic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/104—Aromatic fractions
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/106—Naphthenic fractions
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/044—Cyclic ethers having four or more ring atoms, e.g. furans, dioxolanes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/046—Hydroxy ethers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
- C10M2207/128—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/22—Acids obtained from polymerised unsaturated acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/221—Six-membered rings containing nitrogen and carbon only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
- C10M2215/226—Morpholines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/30—Heterocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
Definitions
- the present invention is directed toward a novel rust inhibiting composition and, more particularly, to a combination of rust inhibitors in a suitable lubricating medium, wherein the slushing oil so provided has enhanced rust inhibiting characteristics due to the presence of a metal salt of a mahogany or naphthalene sulfonic acid and a higher fatty acid of 1560 carbon atoms.
- rust inhibiting compositions which, when applied as a coating, will have the effect of preventing the formation of rust over extended periods of time.
- the coating of a rust inhibiting paint has been applicable where the iron object is stationary and, accordingly, not subject to wear, etc., as would be the case if the iron object was part of a moving mechanism. Therefore, in such environment, wherein the object is stationary, a thick rust inhibiting coating of paint is generally capable of preventing rust over extended periods of time.
- a rust inhibiting composition comprising in combination a metal salt of a phosphate ester or a mixture of phosphate esters, plus an aliphatic carboxylic acid of -60 carbon atoms, e.g., a dimer acid.
- a further combination of a metal salt of a mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid, e.g., dimer acid, in a lubricating oil medium in the presence of a cosolvent provides further enhanced rust inhibition characteristics and such composition is eminently suitable for the inhibiting of rust of iron objects subject to wear and abrasion.
- It is yet a further object of the present invention to provide such a slushing oil comprising a metal salt of a mahogany or naphthalene sulfonic acid, a higher aliphatic carboxylic acid, e.g., dimer acid, a cosolvent therefor, and a paraffinic or naphthenic lubricating oil.
- Such a combination of components providing enhanced rust inhibiting characteristics is generally employed in combination with (c) a cosolvent for the sulfonate and aliphatic carboxylic acid, and (d) a lubricating oil, e.g., paraffinic or napthenic lubricating oil.
- compositions of the present invention in the form of slushing oils or fluids are particularly adapted for the rust prevention of iron objects subjected to movement generally causing wear and abrasion. It is within this environment that the compositions of the present invention provide for objects and advantages not obtainable with conventional rust inhibiting paints.
- a primary component of the slushing oil or fluid of the present invention comprises a metal salt of a mahogany sulfonic acid or naphthalene sulfonic acid.
- metal salts of mahogany or naphthalene sulfonic acids are materials which are well any sulfonic acid or mahogany sulfonate is meant to embrace any and all of the aforedescribed oil-soluble derivatives well known in the art.
- naphthalene sulfonic acids or naphthalene sulfonates are well known materials which are commercially available.
- naphthalene sulfonates are alkyl substituted naphthalene sulfonic acid derivatives wherein the alkyl groups have from 8 to about 30 carbon atoms.
- suitable naphthalene sulfonates in accordance with the present invention include such materials dioctyl naphthalene sulfonate dinonyl naphthalene sulfonate decyl naphthalene sulfonate dodecyl naphthalene sulfonate tridecyl naphthalene sulfonate tetradecyl naphthalene sulfonate hexadecyl naphthalene sulfonate octadecyl naphthalene sulfonate eicosyl naphthalene sulfonate, etc. 7
- the mahogany or naphthalene sulfonates are employed in the novel rust inhibiting composition of the present invention as their metallic salts.
- the suitable metals for producing the mahogany or naphthalene sulfonate salts are metals of Groups IIA, IIIA and IVA of the Periodic Table. Specifically preferred metals for the production of the metal salts include barium, calcium, strontium, lead and aluminum.
- a suitable mahogany sulfonate comprises Bryton Ba-3ON or Bryton Ca-3ON, respectively being the barium salt and calcium salt of mahogany sulfonate marketed by Bryton Chemical Company, a division of Continental Oil Co.
- Bryton Chemical Company a division of Continental Oil Co.
- the above terms are trademarks of the Bryton Chemical Co.
- a suitable naphthalene sulfonate in accordance with the present invention comprises a material known as NA-SUL-BSN, which is the barium salt of dinonyl naphthalene sulfonate NA-SUL- BSN is a registered trademark for the above identified product which is marketed by the R. T. Vanderbilt Co. Inc.
- the second component of the novel synergistic rust inhibiting composition of the present invention is a higher fatty acid containing from -60 carbon atoms.
- higher fatty acids include linoleic acid, linolenic acid, ricinoleic acid, palmitic acid, stearic acid, or mixtures thereof.
- the preferred fatty acid component of the novel synergistic rust inhibiting composition of the present invention comprises the dimer acids which conventionally contain from -60 carbon atoms.
- a particularly preferred component is dimer acid, adimer of linoleic acid having 36 carbon atoms.
- Suitable commercial dimer acids are sold by Emery Industries under the names of Empol 1010 dimer acid containing 97 percent of the dimer of linoleic acid, 3 percent of the trimer of linoleic aicd, and substantially no mono-basic acids.
- the commercial dimer acids for example, contain varying amounts of the trimer of linoleic acid and mono-basic acid.
- a dimer acid sold as Empol 1022 contains 75 percent of the dimer, 22 percent trimer, and 3 percent mono-basic acids
- Empol 1016 contains 87 percent dimer, 13 percent trimer, with only a trace of mono-basic acids. All such commercial formulations can be advantageously employed in accordance with the present invention,
- dimer acid produced by the dimerization of linoleic acid is not precisely known, it is hypothesized that the dimer acid has a structural formula as follows:
- Typical specifications of a commercial product containing approximately 85 percent of the dimer of linoleic acid, 12 percent of the trim'er of linoleic acid, and about 3 percent of the monomeric acid are as follows:
- the enhanced rust inhibition associated with the combination of components in accordance with the present invention is achieved when the metal salts of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid are present in amounts from about 10 to about 90 percent and 90 to about 10 percent by weight, respectively.
- the rust inhibiting composition of the present invention containing only the metal salts of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid contains about 20 to percent by weight of such sulfonate and 80 to 20 percent by weight of the higher aliphatic carboxylic acid, e.g., dimer acid.
- COSOLVENT As indicatedabove, the combination of components,- i.e., metal salt of a mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid, is generally employed in the form' of a slushing fluid or oil wherein such components are dissolved in a mineral oil, e.g., paraffinic or naphthenic oil, in the presence of a cosolvent.
- a mineral oil e.g., paraffinic or naphthenic oil
- the cosolvent for the metal salt of mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid can comprise an aromatic or heterocyclic solvent, or a vari-
- a class of well known glycol ethers is particularly adapted for use in accordance with the present invention.
- such a preferred class of cosolvents includes the monoand dialkyl ethers of ethylene, diethylene and triethylene glycols and similar propylene glycols wherein the alkyl group contains from I to 6 carbon atoms.
- Such preferred cosolvents employed in accordance with the present invention are exemplified by ethylene glycol monobutyl ether.
- any material which acts as a solvent for both the metal salt of the mahogany or naphthalene sulfonic acid and dimer acid can be advantageously utilized in accordance with the present invention and the selection of a proper solvent is governed primarily by such solubility considerations. Accordingly, while the above list is exemplary, it is not in any way meant to embrace all of the conventional solvent materials which can be advantageously utilized in accordance with the rust inhibiting composition of the present invention.
- the novel rust inhibiting composition of the present invention is generally employed in the form of a slushing oil or fluid wherein a mineral oil comprises the vehicle therefor.
- the mineral oil vehicle may be a paraffinic or naphthenic oil ranging in viscosity from 50 to 300 SUS at 100F.
- Naphthenic oils are preferred in accordance with the present invention since the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid are more readily soluble in naphthenic type oils.
- the vehicle in accordance with the present invention can comprise other well known petroleum based oils and lubricants.
- the vehicle for the slushing oil or fluid having enhanced rust inhibiting characteristics can comprise a conventional ester type lubricant, silicon oil, etc.
- the vehicle for the slushing oil fluid be a paraffinic or naphthenic oil, preferably a naphthenic oil, ranging in viscosity from 50 to 300 SUS at 100F.
- the amount of the various components are generally as follows:
- the final composition is generally prepared merely by adding and mixing the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid to the mineral oil vehicle with subsequent addition of the cosolvent, preferably the glycol ether. After a homogeneous solution is prepared by mixing, a final amount of mineral oil is added to the system to bring the same up to the final concentration and to provide the homogeneous mixture having enhanced rust inhibiting characteristics.
- the composition ofthe present invention provides for enhanced or synergistic rust inhibition.
- the use of the combination of the metal salt of the mahogany or naphthalene sulfonic acid and higher aliphatic carboxylic acid, i.e., dimer acid provides for a rust inhibition which is greater than would be expected from the rust inhibiting characteristics of the individual components alone.
- the composition of the present invention acts both as a rust inhibitor and a lubricant, the same is superior to conventional paint rust inhibitors and can be utilized in those environments wherein an iron object is not stationary and wherein due to movement, the same is normally subjected to wear and abrasion. Accordingly, this constitutes a distinct advantage of the novel compositions of the present invention over conventional rust inhibiting compositions.
- EXAMPLE 1 Some 19.98 g. of a 30 percent solution of the barium salt of mahogany sulfonate (Bryton Ba-3ON) in a mineral oil SUS solvent refined naphthenic pale oil) were placed in a 16 oz. widemouth, screw-cap bottle.
- barium salt of mahogany sulfonate Bryton Ba-3ON
- SUS solvent refined naphthenic pale oil SUS solvent refined naphthenic pale oil
- dimer acid (Empol 1022) were added. The mixture was blended until homogeneous. Then 9.0 g. of ethylene glycol monobutyl ether were added and the mixture was blended until homogeneous.
- Table 1 (Rust protection shown by individual components in 100 SUS solvent refined naphthenic pale oil) Additive and Days Protection A homogeneous mixture consisting of 2 percent calcium salt of mahogany sulfonate, Bryton Ca-3ON p 2 percent dimer acid, Empol 1022 3 percent ethylene glycol monobutyl ether 93 percent mineral oil was prepared and tested for rust inhibition in the same manner as described for Example 1. Coated panels remained without rust for 4 days in the Q.C.T. cabinet and for 52 days in the humidity cabinet. Comparing this performance with that of the individual components in Table 1 again shows the superior performance of the combination of ingredients with regard to rust inhibition. 1
- EXAMPLE 3 Some 12 g. of a 50 percent solution of the barium salt of dinonyl naphthalene sulfonate in a mineral oil were placed in a 16 02., wide-mouth, screw-cap bottle.
- dimer acid (Empol 1022)
- the mixture was blended until homogeneous.
- 9 g. of ethylene glycol monobutyl ether were added.
- the foregong examples clearly illustrate that the combination of a metal salt of mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid, e.g., dimer acid, provides for enhanced or synergistic results with regard to rust inhibition.
- a metal salt of mahogany or naphthalene sulfonic acid and a higher aliphatic carboxylic acid, e.g., dimer acid provides for enhanced or synergistic results with regard to rust inhibition.
- the foregoing examples clearly illustrate that since a mineral oil vehicle is employed, the rust inhibiting composition in the form a slushing oil or fluid possesses both rust inhibiting and lubricating properties. Accordingly, this makes the compositions of the present invention eminently suited for use in those environments wherein the iron object normally subject to rusting is also subjected to wear and abrasion.
- a rust-inhibiting slushing oil composition compris- A. 0.5 10 percent by weight of a metal salt of amahogany sulfonate or C alkyl substituted naphthalene sulfonate, said metal being selected from groups IlA, "IA and IVA of the Periodic Table;
- composition of claim 1 wherein said metal is selected from Ba, Ca, Sr, Pb and Al.
- component (A) is a metal salt of a mahogany sulfonate.
- component (A) is a metal salt of a C alkyl naphthalene sulfonate.
- composition ofclaim 4 wherein said C alkyl naphthalene sulfonate is dinonyl naphthalene sulfonate.
- composition of claim 1 wherein said higher aliphatic carboxylic acid is a dimer acid.
- composition of claim 6 wherein said dimer acid is a dimer of linoleic acid.
- composition of claim 1 wherein said cosolvent is a monoor dialkyl ether of ethylene glycol wherein the alkyl group contains from l-6 carbon atoms.
- composition of claim 8 wherein said cosolvent is ethylene glycol monobutyl ether.
- composition of claim 1 wherein said mineral oil is selected from paraffinic and naphthenic oils having a viscosity of 50 to 300 SUS at 100F.
- composition of claim 1 wherein said components (A), (.B), (C) and (D) are present in the follow ing amounts:
- a rust-inhibiting additive composition comprising:
- composition of claim 12 wherein said metal is selected from Ba, Ca, Sr, Pb and Al.
- component (A) is a metal salt of a mahogany sulfonate.
- component (A) is a metal salt of a C840 alkyl naphthalene sulfonate.
- composition of claim 12 wherein said higher aliphatic carboxylic acid is a dimer acid.
- composition of claim 17 wherein said dimer acid is a dimer of linoleic acid.
- a rust inhibiting slushing oil composition comprising 2 percent by weight of the barium salt of mahogany sulfonate, 2 percent by weight of a dimer of linoleic acid, 3 percent of ethylene glycol monobutyl ether, and 93 percent by weight of a mineral oil.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Abstract
Description
Claims (19)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00084540A US3857789A (en) | 1970-10-27 | 1970-10-27 | Slushing oil or rust inhibiting compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00084540A US3857789A (en) | 1970-10-27 | 1970-10-27 | Slushing oil or rust inhibiting compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
US3857789A true US3857789A (en) | 1974-12-31 |
Family
ID=22185607
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00084540A Expired - Lifetime US3857789A (en) | 1970-10-27 | 1970-10-27 | Slushing oil or rust inhibiting compositions |
Country Status (1)
Country | Link |
---|---|
US (1) | US3857789A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4224173A (en) * | 1978-06-12 | 1980-09-23 | Michael Ebert | Lubricant oil containing polytetrafluoroethylene and fluorochemical surfactant |
US4264653A (en) * | 1979-09-24 | 1981-04-28 | Pennwalt Corporation | Coating of steel |
US4396515A (en) * | 1980-03-28 | 1983-08-02 | Cincinnati Vulcan Company | Coating oil compositions |
US4834894A (en) * | 1980-12-29 | 1989-05-30 | Tribophysics Corporation | PTFE oil additive |
US5001013A (en) * | 1989-08-15 | 1991-03-19 | Cincinnati-Vulcan Company | Coating oil having improved electrocoat compatibility |
US5741763A (en) * | 1995-12-22 | 1998-04-21 | Exxon Research And Engineering Company | Lubricant oil composition |
US20140303055A1 (en) * | 2006-03-29 | 2014-10-09 | Kyodo Yushi Co., Ltd. | Lubricant Composition |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2481372A (en) * | 1946-09-27 | 1949-09-06 | Shell Dev | Rust protective lubricants |
US2624708A (en) * | 1950-06-23 | 1953-01-06 | Union Carbide & Carbon Corp | Inhibited polyoxyalkylene glycol fluids |
US2631979A (en) * | 1950-08-30 | 1953-03-17 | Standard Oil Dev Co | Rust inhibiting composition |
US2632695A (en) * | 1951-09-20 | 1953-03-24 | Socony Vacuum Oil Co Inc | Rust inhibitor for light petroleum products |
US2632694A (en) * | 1950-11-14 | 1953-03-24 | Sinclair Refining Co | Petroleum distillates containing ammonium mahogany sulfonates and oil soluble carboxylic acids to prevent corrosion |
US2671758A (en) * | 1949-09-27 | 1954-03-09 | Shell Dev | Colloidal compositions and derivatives thereof |
US2739126A (en) * | 1954-01-25 | 1956-03-20 | Bray Chemical Company | Corrosion preventive oils |
US2773036A (en) * | 1951-12-27 | 1956-12-04 | Tidewater Oil Company | Extreme pressure soluble oil compositions |
US2883277A (en) * | 1956-10-12 | 1959-04-21 | Gen Aniline & Film Corp | Synergistic corrosion inhibiting composition for gasoline |
US2904415A (en) * | 1956-05-23 | 1959-09-15 | Nat Aluminate Corp | Non-corrosive petroleum distillates |
CA615549A (en) * | 1961-02-28 | B. Sheldahl David | Water dispersible slushing composition | |
US3004917A (en) * | 1959-05-14 | 1961-10-17 | Exxon Research Engineering Co | Oil compositions containing rust inhibitors |
US3242078A (en) * | 1960-12-16 | 1966-03-22 | Exxon Research Engineering Co | Suspending colloidal calcium carbonate in hydrocarbon oils |
US3242079A (en) * | 1962-04-06 | 1966-03-22 | Lubrizol Corp | Basic metal-containing thickened oil compositions |
-
1970
- 1970-10-27 US US00084540A patent/US3857789A/en not_active Expired - Lifetime
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA615549A (en) * | 1961-02-28 | B. Sheldahl David | Water dispersible slushing composition | |
US2481372A (en) * | 1946-09-27 | 1949-09-06 | Shell Dev | Rust protective lubricants |
US2671758A (en) * | 1949-09-27 | 1954-03-09 | Shell Dev | Colloidal compositions and derivatives thereof |
US2624708A (en) * | 1950-06-23 | 1953-01-06 | Union Carbide & Carbon Corp | Inhibited polyoxyalkylene glycol fluids |
US2631979A (en) * | 1950-08-30 | 1953-03-17 | Standard Oil Dev Co | Rust inhibiting composition |
US2632694A (en) * | 1950-11-14 | 1953-03-24 | Sinclair Refining Co | Petroleum distillates containing ammonium mahogany sulfonates and oil soluble carboxylic acids to prevent corrosion |
US2632695A (en) * | 1951-09-20 | 1953-03-24 | Socony Vacuum Oil Co Inc | Rust inhibitor for light petroleum products |
US2773036A (en) * | 1951-12-27 | 1956-12-04 | Tidewater Oil Company | Extreme pressure soluble oil compositions |
US2739126A (en) * | 1954-01-25 | 1956-03-20 | Bray Chemical Company | Corrosion preventive oils |
US2904415A (en) * | 1956-05-23 | 1959-09-15 | Nat Aluminate Corp | Non-corrosive petroleum distillates |
US2883277A (en) * | 1956-10-12 | 1959-04-21 | Gen Aniline & Film Corp | Synergistic corrosion inhibiting composition for gasoline |
US3004917A (en) * | 1959-05-14 | 1961-10-17 | Exxon Research Engineering Co | Oil compositions containing rust inhibitors |
US3242078A (en) * | 1960-12-16 | 1966-03-22 | Exxon Research Engineering Co | Suspending colloidal calcium carbonate in hydrocarbon oils |
US3242079A (en) * | 1962-04-06 | 1966-03-22 | Lubrizol Corp | Basic metal-containing thickened oil compositions |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4224173A (en) * | 1978-06-12 | 1980-09-23 | Michael Ebert | Lubricant oil containing polytetrafluoroethylene and fluorochemical surfactant |
US4264653A (en) * | 1979-09-24 | 1981-04-28 | Pennwalt Corporation | Coating of steel |
US4396515A (en) * | 1980-03-28 | 1983-08-02 | Cincinnati Vulcan Company | Coating oil compositions |
US4834894A (en) * | 1980-12-29 | 1989-05-30 | Tribophysics Corporation | PTFE oil additive |
US5001013A (en) * | 1989-08-15 | 1991-03-19 | Cincinnati-Vulcan Company | Coating oil having improved electrocoat compatibility |
US5741763A (en) * | 1995-12-22 | 1998-04-21 | Exxon Research And Engineering Company | Lubricant oil composition |
US20140303055A1 (en) * | 2006-03-29 | 2014-10-09 | Kyodo Yushi Co., Ltd. | Lubricant Composition |
US9376644B2 (en) * | 2006-03-29 | 2016-06-28 | Kyodo Yushi Co., Ltd. | Lubricant composition |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4053426A (en) | Lubricant compositions | |
CA1283399C (en) | Grease composition | |
US2956020A (en) | Anti-corrosion compositions | |
US4193882A (en) | Corrosion inhibited lubricant composition | |
US2631979A (en) | Rust inhibiting composition | |
US2481372A (en) | Rust protective lubricants | |
JPS58171488A (en) | Lubricating oil composition | |
US2775560A (en) | Corrosion inhibitting lubricating compositions | |
US2412634A (en) | Lubricant | |
US2564422A (en) | Corrosion preventive composition | |
US3857789A (en) | Slushing oil or rust inhibiting compositions | |
US3004916A (en) | Lubricating oil | |
FI85159C (en) | Useful reaction product of triaxol and amine phosphate in lubricant | |
US2382699A (en) | Slushing oil compositions | |
US3169116A (en) | Corrosion inhibiting compsoitions | |
EP0295108B1 (en) | Corrosion inhibiting composition | |
US2602049A (en) | Antioxidants for mineral oil lubricants and compositions containing the same | |
US3121057A (en) | Succinamic metal salts in turbine oil | |
US2908648A (en) | Corrosion-inhibited compositions containing n-(alkylarylsulfonyl) amino acids and salts thereof | |
US4052322A (en) | Corrosion-inhibited grease compositions | |
US2533300A (en) | Morpholine mahogany sulfonate as a rust inhibitor for petroleum oils | |
US3214377A (en) | Phenylamides of organoamine polyacetic acids as anti-oxidants in greases | |
US2359738A (en) | Rust-preventive compositions | |
US3203896A (en) | Lubricating composition | |
US3359202A (en) | Lubricating compositions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: CHASE MANHATTAN BANK, THE NATIONAL ASSOCIATION Free format text: SECURITY INTEREST;ASSIGNOR:DORSET INC. A CORP OF DELAWARE;REEL/FRAME:005122/0370 Effective date: 19890329 |
|
AS | Assignment |
Owner name: GAF CHEMICALS CORPORATION Free format text: CHANGE OF NAME;ASSIGNOR:DORSET INC.;REEL/FRAME:005251/0071 Effective date: 19890411 |
|
AS | Assignment |
Owner name: RHONE-POULENC SPECIALTY CHEMICALS, L.P., NEW JERSE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:GAF CHEMICALS CORPORATION;REEL/FRAME:005315/0588 Effective date: 19900404 |
|
AS | Assignment |
Owner name: DORSET INC., A DE CORP. Free format text: CHANGE OF NAME;ASSIGNOR:GAF CORPORATION, A DE CORP.;REEL/FRAME:005250/0940 Effective date: 19890410 |
|
AS | Assignment |
Owner name: DORSET INC., Free format text: RELEASED BY SECURED PARTY;ASSIGNOR:CHASE MANHATTAN BANK, THE,;REEL/FRAME:005597/0269 Effective date: 19890329 |
|
AS | Assignment |
Owner name: RHONE - POULENC SPECIALITY CHEMICALS Free format text: A CORRECTIVE ASSIGNMENT TO CORRECT THE SINGLE SERIAL NUMBER 07194,259 IDENTIFIED IN PREVIOUSLY RECORDED ASSIGMENT ON REEL 5315/FRAME 589.;ASSIGNOR:GAF CHEMICALS CORPORATION;REEL/FRAME:005722/0439 Effective date: 19910513 |
|
AS | Assignment |
Owner name: RHONE-POULENC SURFACTANTS AND SPECIALTIES INC., NE Free format text: CHANGE OF NAME;ASSIGNOR:RHONE-POULENC SPECIALTY CHEMICALS INC.;REEL/FRAME:005748/0167 Effective date: 19910123 Owner name: RHONE-POULENC SURFACTANTS AND SPECIALTIES, L.P. Free format text: CHANGE OF NAME;ASSIGNOR:RHONE-POULENC SPECIALTY CHEMICALS, L.P.;REEL/FRAME:005753/0422 Effective date: 19900430 |