CA2299857A1 - Corrosion inhibitor and process - Google Patents

Corrosion inhibitor and process

Info

Publication number
CA2299857A1
CA2299857A1 CA 2299857 CA2299857A CA2299857A1 CA 2299857 A1 CA2299857 A1 CA 2299857A1 CA 2299857 CA2299857 CA 2299857 CA 2299857 A CA2299857 A CA 2299857A CA 2299857 A1 CA2299857 A1 CA 2299857A1
Authority
CA
Grant status
Application
Patent type
Prior art keywords
process
alkanolamine
composition
acid
comprises
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.)
Abandoned
Application number
CA 2299857
Other languages
French (fr)
Inventor
Gerald H. Kyle
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CHEMAX Inc
Original Assignee
Gerald H. Kyle
Chemax, Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M173/00Lubricating compositions containing more than 10% water
    • C10M173/02Lubricating compositions containing more than 10% water not containing mineral or fatty oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/26Carboxylic acids; Salts thereof
    • C10M129/28Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M129/38Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
    • C10M129/42Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
    • C10M133/04Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M133/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M133/08Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12Reaction products
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • C23F11/14Nitrogen-containing compounds
    • C23F11/141Amines; Quaternary ammonium compounds
    • C23F11/143Salts of amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • 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
    • C10M2207/127Carboxylix 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 polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/22Acids obtained from polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2230/00Specified physical or chemical properties of lubricating compositions
    • C10N2230/12Resistance to rust or corrosion
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/401Metal working with removal of material, e.g. cutting, grinding, drilling
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/402Metal working without removal of material, e.g. forming, gorging, drawing, pressing, stamping, rolling, extruding
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/403Manufacturing joint less pipes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/404Hot working
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/405Cold working
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/406Metal working of specific metals
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/406Metal working of specific metals
    • C10N2240/407Soft metals, e.g. aluminium
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/406Metal working of specific metals
    • C10N2240/408Iron or steel
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2240/00Specified uses or applications of lubricating compositions
    • C10N2240/40Metal working
    • C10N2240/406Metal working of specific metals
    • C10N2240/409Metal working of specific metals stainless steel
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2250/00Form or state of lubricant compositions in which they are used
    • C10N2250/02Emulsions; Colloids; Micelles

Abstract

A corrosion inhibitor composition for metal working and a method for making the same is provided.
The composition is made by reacting maleated tall oil fatty acids with alkanolamines. The alkanolamines suitable for the present invention may be ethanolamines or other alkanolamines such as di-glycolamine if ethanolamines are not environmentally preferred. The resulting reaction product salts provide an effective corrosion inhibitor suitable for incorporation into aqueous products such as buffing compounds, cutting fluids, drawing compounds, cleaning fluids and forging aids.

Description

CORROSION INHIBITOR AND PROCESS
Field of the Invention The present invention is generally directed to a corrosion inhibitor and a process for using the inhibitor. More particularly, the present invention is directed to a corrosion inhibitor particularly well suited for preventing corrosion during various metal working operations.
Background of the Invention This invention relates to corrosion inhibitors used in metal working. As used herein, metal working includes, but is not limited to, metal polishing, cutting, grinding, stamping, cleaning, drawing, forming, forging, and other processes where metal oxidation and corrosion is a problem.
It is well known in the metal working industries to combine corrosion inhibitors with cutting fluids, cleaners, and drawing compounds. Traditionally, typical inhibitors employ alkyl diacids of C6 to Clz chain length such as dodecanedioic acid to protect the metal.
U.S. Patent No. 5,292,480 to Fischer, et al.
Discloses a corrosion inhibitor for metal parts which is produced by reacting a fatty acid Diels-Alder adduct or fatty acid-ene with a polyalcohol to form an acid-anhydride ester corrosion inhibitor. The resulting ester may be further reacted with amines, metal hydroxides, metal oxides, ammonia, and combinations thereof to neutralize the ester. The corrosion inhibitor is disclosed as having utility for controlling corrosion in down-hole oil field and piping equipment.
U.S. Patent No. 5,643,534 to Minevski discloses a corrosion inhibiting composition supplied as a concentrate which includes a blend of salicylic acid;
a reaction product of maleated tall oil fatty acid polyhydroxy polyalkane and ammonium or potassium hydroxide; tallow diamine quaternary dichloride or alkanediol; and alkanol or alkanolamine. The inhibitor is disclosed as being useful in acid gas removal amine units which employ alkanol amine solutions.
While these corrosion inhibitors are believed satisfactory for their intended purposes, there exists room for improvement within the art. The present invention is an improvement in that it provides an effective corrosion inhibitor which is cost effective, easy to manufacture, and affords superior corrosion protection. A preferred embodiment of the composition has been found useful as an aqueous-based corrosion inhibitor which is compatible with a variety of metal working formulations and processes.
Summary of the Invention It is an object of the present invention to provide a composition useful as a corrosion inhibitor for metal working applications.
It is another object of the present invention to provide a corrosion inhibitor composition which is compatible with conventional additives used in the metal working industry.
It is a further and more particular object of this invention to provide a corrosion inhibitor with a broad range of utility and which has low toxicity.
It is a further object of this invention to provide a process of preventing corrosion in worked metals which comprises the use of a reaction product of a maleated tall oil fatty acid with one or more alkanolamines.
These and other objects of the present invention are achieved by providing a metal corrosion inhibitor composition. The corrosion inhibitor composition includes a reaction product of a maleated tall oil fatty acid with an alkanolamine. The alkanolamine can be, for instance, an ethanolamine, such as monoethanolamine, triethanolamine, and mixtures thereof. When in use, the corrosion inhibitor composition of the present invention can be contained in a dilute aqueous solution. For instance, the corrosion inhibitor composition can be present in the solution in an amount up to about 20% by weight, and particularly in an amount up to about 5% by weight.
In one embodiment of the present invention, the corrosion inhibitor composition can further include a reaction product of an alkanolamine and a C6 to ClB
alkyl carboxylic acid. The C6 to C1$ alkyl carboxylic acid can be, for example, neodecanoic acid, isononanoic acid, and mixtures thereof.
The metal corrosion inhibitor composition of the present invention is well suited to protecting metals when the metals are contacted with fluids, such as water, that can cause corrosion. For example, in one embodiment, the corrosion inhibitor of the present invention can be incorporated into a lubricating solution that lubricates the metal during metal working operations. The corrosion inhibitor composition can also be incorporated into rinsing solutions.

Description of Preferred Embodiments It is to be understood by one of ordinary skill in the art that the present discussion is a description of exemplary embodiments only, and is not intended as limiting the broader aspects of the present invention, which broader aspects are embodied in the exemplary construction.
A composition and process for treating metals, especially ferrous metals, to prevent corrosion are provided. Generally, the composition comprises a reaction mixture of a maleated tall oil fatty acid with one or more alkanolamines. Maleated tall oil fatty acid is known as an intermediate chemical for various corrosion inhibitors. However, the specific reaction products of the present invention offer improved qualities over other known derivatives of maleated tall oil fatty acid. The resulting reaction products of the present invention comprise alkanolamine salts of the maleated tall oil fatty acid and afford excellent corrosion resistance to worked metals. The reaction product(s)are water soluble; are compatible with typical metal working additives commonly used in metal finishing, buffing compounds, cutting fluids, and other metal working compounds; and have low toxicity.
An additional advantage of the present compositions and process is the ease of manufacture.
The present inhibitor formulation is made according to a process which takes place in simple reactor vessels at ambient laboratory conditions and pressures. While the reaction is slightly exothermic, no external pressure or temperature regulation is required.

Further, the reaction proceeds quickly, in contrast to conventional teachings where elevated pressures, temperatures and/or reaction times are needed.
As described above, in general, the corrosion 5 inhibitor composition of the present invention includes the reaction products of a maleated tall oil fatty acid with one or more alkanolamines.
Alkanolamines that may be used in the present invention can vary depending upon the particular application and the particular result desired. For most applications, ethanolamines can be used to neutralize the maleated tall oil fatty acid.
Particular ethanolamines that can be used include triethanolamine and monoethanolamine. In fact, it has been discovered that when a mixture of triethanolamine and monoethanolamine are used to neutralize the tall oil fatty acid, superior results are achieved. For instance, a triethanolamine and monoethanolamine mixture can be used to neutralize the fatty acid in which triethanolamine is present in the mixture in an amount of at least 30% by weight, particularly at least 50% by weight and, in one embodiment, present in an amount of about 66% by weight.
In general, one or more alkanolamines are combined with a maleated tall oil fatty acid in an amount sufficient to completely neutralize the fatty acid. Preferably, excess amounts of alkanolamines are present. For most applications, the weight ratio of alkanolamines to the maleated tall oil fatty acid is about 2 to 1.
Besides at least one alkanolamine and the maleated tall oil fatty acid, the reaction mixture of the present invention can include various other ingredients. For instance, various additives can be included in order to facilitate the reaction or in order to enhance the final properties of the composition. For example, in one embodiment, one or more alkyl carboxylic acids having from a C6 to a Cla carbon chain may be added to the reaction mixture.
Specifically, the alkyl carboxylic acid can be added in order to improve the properties of the final product. During the reaction, the alkyl carboxylic acid also becomes neutralized by the alkanolamines.
Examples of alkyl carboxylic acids that may be used in the process of the present invention include neodecanoic acid and isonononoic acid.
Once reacted, the corrosion inhibitor composition of the present invention should generally have a pH of greater than about 6, and preferably has a pH of greater than about 7. In one embodiment, the composition can have a pH of from about 7 to about 9.
It should be understood, however, that higher pHs are possible.
When used in metal working applications, the reaction products of the present invention can be combined in an aqueous solution. For most applications, the corrosion inhibitor composition of the present invention can be heavily diluted with water during use. For instance, the concentration of the reactant products in an aqueous solution during use is typically from about 0.25% to about 1% by weight.
The corrosion inhibitor of the present invention has been found to be compatible with a variety of standard additives found in metal working applications. For instance, the corrosion inhibitor composition can be combined with other corrosion inhibitors, surfactants, and lubricants.
For instance, in one embodiment of the present invention, the corrosion inhibitor composition can be contained within a lubricating solution that is intended to treat metal substrates when the substrates are subjected to various metal working processes.
Examples of surfactants that may be used with the composition of the present invention include, but are not limited to, fatty acid alkoxylates, fatty amine alkoxylates, alcohol alkoxylates, alkylphenol alkoxylates, castor oil alkoxylates, phosphate esters and polyols. Further, it is believed that any ethoxylated or propoxylated derivative may be combined and used with the composition of the present invention.
Metal lubricants that may be used with the composition of the present invention include most synthetic or nonsynthetic lubricants. Examples of lubricants include, for instance, mineral oil, vegetable oil, fatty esters, polyol esters, and any of the above described surfactants, which sometimes also serve as lubricants. In general, when treating metals, a lubricant solution can contain a lubricant in an amount up to about 80% by weight, particularly in an amount up to about 50% by weight, and more particularly in an amount from about 3% to about 40%
by weight. The remainder of the solution can include the corrosion inhibitor composition of the present invention, any surfactants, and water.

When in use, a lubricating composition is typically applied to a metal while the metal is being subjected to some type of process, such as a forming, cutting, stamping, drawing, polishing, grinding, or forging process. After the metal has been worked, the lubricating solution containing the corrosion inhibitor composition of the present invention is typically washed off. Of particular advantage, as described above, the corrosion inhibitor composition of the present invention is nontoxic and thus can be easily disposed of.
Besides being contained in a lubricating solution, the corrosion inhibitor composition of the present invention can also be contained in the rinsing solution and in other various solutions that contact the metal.

Example 1 A first preferred embodiment of the present invention is provided by the reaction of a maleated tall oil fatty acid (herein after "tall oil"), such as that available from Westvaco as TENAX 2010, with a mixture of alkanolamines, such as monoethanolamine (MEA) and triethanolamine (TEA). The maleated tall oil fatty acid used herein, has a monomer content of less than about 10%.
The reaction products are obtained as follows:
A 24.4% by weight of water is placed in a reaction vessel with stirring. 12.2% by weight of MEA
(Dow; Union Carbide) and 37.8% by weight of TEA (Dow;
Union Carbide) are added to the water with constant stirring or agitation. Once throughly mixed, 25.6% by weight of TENAX 2010 brand of tall oil is slowly added with constant stirring. The resulting exothermic reaction is allowed to proceed for approximately 30 minutes. A final pH of between 7-9 is obtained for the reaction product and may be adjusted using additional TEA or other similar acids.
The resulting reaction products are the amine salts of a polycarboxylic acid such as the tricarboxylic acid set forth below. The reaction products are in the form of a viscous, dark amber solution. The reaction and resulting reaction products are set forth in the following equation:

O
.. ~~
H 0 ~~"~ ~~ CH3 (CHZ~x H(CH~ ~ COH ~' H2NCH2CH20H + .'N ~ CHICHiOH?3---->
O O

10 , CH3 (CHZ~X H(CHi ~Y CO : ~3 X+Y=12 .X+Y=12 O ' + +
D ~ . 'D~ .~ ' ~ .
..~ , +
where D~ +, DZ + and D~ + =-H~NCHiCH20H or HN(CHZCHZOH}~.
As set forth in Examples 2 and 3, additional carboxylic acids such as neodecanoic acid and isonononoic acid may be added/reacted along with the tall oil. The reaction products and formulations set forth herein, provide a stable, versatile, water soluble corrosion-inhibiting formulation which is compatible with a variety of additional additives, including surfactants, lubricants, and other inhibitors.
The reaction mixture's primary products are the salts referenced in the reaction products above. A
small percentage of an ester amide reaction product may be present, but such products are not thought to significantly contribute to the corrosion inhibiting properties seen herein.
As set forth in the examples below, the combination of approximately 3 parts of TEA to 1 part of MEA has been found to perform best under the described test conditions. However, the use of TEA as the sole alkanolamine also provides a reaction product useful as a corrosion inhibitor. Beneficial results are achieved using diethanolamine (DEA) as the alkanolamine. However, as a suspected carcinogen, the use of DEA is not preferred. The formulations described above are preferred and achieve the beneficial results set forth in the additional examples below.
Example 2 A second preferred embodiment of the corrosion inhibitor formulation was prepared as described above, using the ingredients and proportions set forth in Table 1. The stock corrosion inhibitor as set forth in Table 1 was mixed in distilled water to provide working concentrations of 1%, 0.75%,0.5%, and 0.25%.
Each working concentration was used to evaluate the corrosion inhibiting properties with respect to cast iron chips in a open environment. Specifically, the above solutions were tested for their ability to inhibit corrosion according to standard test method ASTM-D4627-86. 10 grams of cast iron chips were placed in contact with a circular filter paper contained within a 9 cm petri dish bottom. 40 mls of the respective concentrations of the corrosion inhibitor were added to the petri dish, uniformly covering and wetting the cast iron chips. Air bubbles were displaced by gentle tapping of the petri dish, ensuring all the iron chips were in contact with the inhibitor solution.
Following an incubation period of 30 minutes, the inhibitor solution was decanted and the excess free fluid was removed. The iron chips were left undisturbed for 24 hours in the open petri container and under standard ambient laboratory conditions.
After 24 hours, the iron chips were removed from the filter paper and the number of rust spots appearing on the paper were recorded. The results are reported based upon the following rankings:
0-5 spots Excellent 5-10 spots Good 10-20 spots Fair >20 spots Poor Observations of the surface of the iron chips were also made. Further, qualitative assessments were possible by comparing the intensity of stains present on the filter paper.

_ CA 02299857 2000-03-02 --g2p 2 2 . 0 ' 2 2 . 0 MEp, ~ 11.0 11.0 TEA 34.0 34.0 TENAX 2010 23.0 23.0 Neodecanoic Acid ~ 10.0 --Isonononoic Acid -- 10.0 Results of Cast Excellent Excellent Iron Chip Test at 1%

Results of Cast Iron Chip Test at Excellent Excellent 0.75%

Results of Cast Iron Chip Test at Excellent Excellent 0.5%

Results of Cast Iron Chip Test at Fair Poor 0.25%

All values are in wt. %.

As seen in reference to Table 1, the corrosion inhibitor provided excellent corrosion protection to the test iron particles.
Example 3 By way of comparison, Table 2 sets forth data on formulations where the maleated tall oil fatty acid was replaced with various carboxylic acids. The carboxylic acids evaluated are known and used for their corrosion inhibiting properties. In each instance, the listed formulations were evaluated using the chip iron protocol of Example 2 and the results reported in Table 2.

0 0 0 0 o s~ ~ ~ ~

I . I . I 1 O '~ ~~ -~-I

O N ~7 I aD 1 ~ 1 I O ~

W
N ~ H

O O O O O

. 1 . . I I I O

O N tf7I GD t17I I I O

N ~

O O O O O S-I

I I I I O ~ cd r>y O cr '-i~ I I I I O O C=.i Cs.~ Cs~

M M .-i cp O O O O O f~

. . . . 1 I I I ri O -rl --1 3 M o ~r ~ ~n 1 I I o I rd O

M M r1 r'I r-1 G4 (3.1 C=.~ f3.1 N --. N

H O O O O O l.1 ~ ~ ~ N

I I I i O

N u7 c .-1O I I I 1 O O ~ ~ ~ r-1 M M rl r-I H Qr [xa Gu Ga H

O O O O O f.-1 I I I I O w"'1 ''~ -''1 tf~C r-1O I I I O i O b ~ b M M .-Ir-1 ~ G1, C~, C~ f~

U ~ s~ s~ t~

-.-1 O O O O

O ~ Sa Sa Sa ~-I
dp o~

H H H H
tl~ dP

U .O 'Z~ f~ ~ N

!J ~ -r1rl 1~ ~ ~ +.~
ow V7 "C~
b -.i -~ ~s_f'L3 U U U U
.I-~+~ ~.~ .I-~

S.a U -rl-rlU U b cd rtS rb ?, ~C U U .-t-rl4-.~w w 4.-a 'U

?~ r.~r..>rO O O O O O
~ +~ ~ ~

U s~ O v1 tn t~ tn -~-1U U r0 O U1 U1 v7 u1 4J N ~ N

N cn -~ -rlU s~ ~ .i-~ ~ ~.-~
H E.~ E-~ C-~

~ W ~ rt1b >~ ~ ~ ~ ~
b -I ~1. ~1. ~1, ~1, -t~ N ~ O O tn cn U1 u7 -~I -~ ~ -~-I -.-a U U

x H~ ~ O ~ ~ ~ Z H c~ rx ~ cx rC U U

Example 4 As set forth in Tables 3 and 4, various combinations of formulations were evaluated using TENAX 2010 in combination with other amino alcohols.
In particular, in this example, the monoethanolamine and the triethanolamine were replaced with the amino alcohols. The protocols and testing procedures used in Example 2 were followed. Results are as reported in Tables 3 and 4.

_.

f~ ~tflO ,-~ f,-I~ --I .-i I O -r1 -.-I ri ~ ~r o c I O

r-~C' N N LL

C t~ l0 M 1~-1'"~ rl ~-i I . O '~ w-I w-i ~ l0 I l0 H O ~ (s.i C~

rl C N r-IGL

r-I r-1 r1 N ~ M S-1 .,1 .,..I

I I O c0 ( ~C7C' I O I O [t, (s, Cxa --i~C7 c~1 0.~

d~P

I O ..., -r-I .~I 3 0 0 0 o I O

N ~i'N N W w w w .-1 N

'-1 ri '-I

I I O ~ ~

N O O O I i O ~ ro ~ ~
i N d' ~' Q'' (sr Cra Cxa H

H

I . I .,~ O .~-i -,-1 O O I O I tt7 O ~d b N C' C' Gc.~O.i C~ Gu dP I s~ s~ s~

O O O O

O '-I S-I 3-1 S-1 LI
oW oW

ri v ?t H H H H
~ oW tn ?i ~ 'b f'~ tn N

~., .J~ r-I1-1 .IJ J, a--~
-I oW dP

+.~ ~ ~ U tn N cn cn O ~ O o O

l ~ ~ ~ t0 N id c~

'b v U U U U
-t-~+~ ~ ~

N O N U N c0 b r0 O ~ rl rl W 4-i 4.a ~1-a I rd I O O O O O O
~ J.-r -a O O. ~ S~ !n U7 U7 tn N O O O rtS b ~ u1 U1 ~
~ N N N

>~ la s~ Cl~ U ~.-~.~-~ +-~ ~
,-. -- E-~ E-~ E1 H

..-I w O N ~ ~ .-m -i f~

U ~ 1.a "O ~ ~ ~ ~
U ~'1.S1~ f,.l~Cl o z ~ M ~ a, o ,~ >~

N W ' O O N ~ N Q ~
.C ,~ .s~

x E-~N ~ N ~ z fx !.~ ~ rx U U U U U U

__ N ~ M O ~r-1 -rl -r-I

1 1 ~ I

~ L,a f.~ Crr 0~ tt'I I I~ 1 N

N lf7 M S-1 .--1 r-I r-1 1 . I I O .,..I _ 0~ c' i t~ I 1 ~

w w Ga -i ~ N

(~'~N .-i f~ l~ 1,"~ r-~i r-i ~-I

i . . O

~ l0 M I f~ ~ ~

Gu Cz.i Cu v-IcP N

C~ C~ ~' t1' CO ~1 r-1 r~ ri .~ .,..I

l0 '-1O O O I O

~-1C ~-I .-i N ~

s~

M
1 O O O 1 ~1 r-I. r--I ~ O

I ' I 1 0 b b N N W C~ L=-r C~

H N

O O O S-I '-1 r-I '-"'I

1 . . 1 . I O W W

N I O ~ I ~ I

~ N N

O O f'-1 ~-i ~-I ~-I

''IO O ~(7 tn O c0 cd b N N ~ ~ ~ Cia C=.~ Cza O O

N ~

~I .-W , d,~ .rJ ~ +~

?~ O .s~ 'd cd c~ b td tn ~ -~ b U O U v~ v~ -I-~rn .~.~tn -a ~

N O ~ ~ ~ rb c>J rb v1 N N
u7 U7 b U O U O U O U O

I N ~ ~ ~' E-N

O i~, ~ O -.iw ~+-~ ~ ~
.

,-~I O I c0 S-~ O O ~ O G. O 0. O ~1, U

O fa ~ fa-. C1 :~ -.a -.~ .~-.I .~I

N O C1r O O O b U1 U7 .~ U1 ~ U1 O .C .C

U s~ u7 U ~ U ~ U ~ U ~ U
1-t -, f'7 -r-I -ri cU r-I r--i rl r-1 , N o'P 0~

. ow ~ U O ~ 'b ~ S~ ~ s~ ~ C ~ :~
~ oW ~

o z ~ r, b ~ ~ -~I o ~n ~n o ~n o ~n ~n ~ o c~ ~ o N

N W ~ O O ~ ~ ~ S-1 ~ S-I ~ ~-I ~ S-1 dP

..'L',E-~N 1 N I ,~, Z, f~-i CG H fY., (=C, " U ~ f"~ O H O H
H O

As set forth above, the preferred embodiment of the corrosion inhibitor affords significant corrosion protection to the test metals. Compositions replacing the tall oil with other carboxylic acids (Table 2) resulted in products which performed poorly compared to the tall oil reaction products of the present invention. Similar substitution efforts with respect to the preferred alkanolamines (Table 3 and 4), also failed to achieve results as good as the preferred compositions. The combination of MEA/TEA with the maleated tall oil produces a reaction product having superior performance qualities. In fact, a true synergy is achieved in the preferred combinations when compared to the corrosion inhibiting properties of the various reagents as evaluated in Tables 3 and 4.
The preferred embodiment of the present invention has demonstrated its effectiveness compared to other corrosion inhibitors evaluated. The corrosion inhibitors of the present invention offer greater protection than conventional inhibitors. Further, the present formulation achieves improved results while using lower concentrations than prior art formulations. Accordingly, the present formulations are advantageous in terms of economy of cost as well as effectiveness.
It will be understood that the invention is not limited to the particular embodiments or processes described herein, nor the particular parameters or dimensions described therefor. It should also be understood that other basic fatty acid material equivalent to that described falls within the scope of the present invention. Preparation routes of the compositions and process steps therefore are merely exemplary so as to enable one of ordinary skill in the art to employ the method and compositions described herein and used in accordance with the present 5 process. It will also be understood that while the form of the invention shown and described herein constitutes a preferred embodiment of the invention, this description is not intended to illustrate all possible forms of the invention. Aspects of the 10 various embodiments may be interchanged both in whole or in part. The words used are words of description rather than of limitation. Various changes and variations may be made to the present invention without departing from the spirit and scope of the 15 following claims.

Claims (29)

1. A metal corrosion inhibitor composition comprising:
a reaction product of a maleated tall oil fatty acid with an alkanolamine.
2. The composition as defined in claim 1, wherein said alkanolamine is an ethanolamine selected from the group consisting of monoethanolamine, triethanolamine, and mixtures thereof.
3. The composition as defined in claim 2, wherein said reaction products have a general chemical structure consisting of:
4. The composition according to claim 1, wherein said maleated tall oil fatty acid and said alkanolamine is reacted in the presence of neodecanoic acid.
5. The composition according to claim 1, wherein said maleated tall oil fatty acid and said alkanolamine is reacted in the presence of isonononoic acid.
6. The composition according to claim 1, wherein said maleated tall oil fatty acid and said alkanolamine is reacted in the presence of a mixture of isonononoic acid and neodecanoic acid.
7. The composition according to claim 2, wherein about 1 part of said maleated tall oil fatty acid is present to about 2 parts of said alkanolamines.
8. The composition according to claim 1, wherein said maleated tall oil fatty acid and said alkanolamine are reacted in the presence of a C6 to C18 alkyl carboxylic acid.
9. The composition according to claim 1, wherein said composition comprises an aqueous solution.
10. The composition according to claim 2, wherein said alkanolamine comprises a mixture of monoethanolamine and triethanolamine, and wherein about 1 part of said monoethanolamine is present to about 3 parts of said triethanolamine.
11. The composition as defined in claim 1, wherein, said alkanolamine comprises a material selected from the group consisting of a glycolamine, tri-isopropanolamine, mono-isopropanolamine, and mixtures thereof.
12. A process of inhibiting corrosion of metals, said method comprising adding to a metal an effective amount of an aqueous solution containing a corrosion inhibiting composition, said composition comprising a reaction product of a maleated tall oil fatty acid and an alkanolamine.
13. The process as defined in claim 12, wherein said alkanolamine comprises at least one ethanolamine.
14. The process according to claim 13, wherein said ethanolamine is triethanolamine.
15. The process according to claim 13, wherein said ethanolamine is monoethanolamine.
16. The process according to claim 13, wherein said ethanolamine is a mixture of monoethanolamine and triethanolamine.
17. The process according to claim 16, wherein said mixture of monoethanolamine and triethanolamine contains at least 50% by weight triethanolamine.
18. A process as defined in claim 12, wherein said corrosion inhibiting composition further comprises a reaction product of an alkanolamine with a C6 to C12 alkyl carboxylic acid.
19. The process according to claim 18, wherein said C6 to C18 alkyl carboxylic acid comprises a material selected from the group consisting of neodecanoic acid, isonononoic acid and mixtures thereof.
20. The process according to claim 12, wherein said alkanolamine comprises a material selected from the group consisting of a glycolamine, tri-isopropanolamine, mono-isopropanolamine, and mixtures thereof.
21. A process for working metals, said process comprising the steps of:
providing a metal substrate;
contacting said metal substrate with an aqueous solution, said aqueous solution containing a lubricant and a corrosion inhibitor, said corrosion inhibitor comprising a reaction product of a maleated tall oil fatty acid and an alkanolamine; and working said treated metal substrate in order to modify the shape of said substrate.
22. A process as defined in claim 21, wherein said alkanolamine comprises at least one ethanolamine.
23. A process as defined in claim 22, wherein said ethanolamine comprises monoethanolamine.
24. A process as defined in claim 22, wherein said ethanolamine comprises triethanolamine.
25. A process as defined in claim 22, wherein said ethanolamine comprises a mixture of triethanolamine and monoethanolamine.
26. A process as defined in claim 25, wherein said mixture of said monoethanolamine and triethanolamine comprises at least 50% by weight triethanolamine.
27. A process as defined in claim 21, wherein said aqueous solution further comprises a surfactant.
28. A process as defined in claim 21, wherein said corrosion inhibitor further comprises a reaction product of an alkanolamine and a material selected from the group consisting of neodecanoic acid, isonononoic acid, and mixtures thereof.
29. The process according to claim 21, wherein said alkanolamine comprises a material selected from the group consisting of a glycolamine, tri-isopropanolamine, mono-isopropanolamine, and mixtures thereof.
CA 2299857 1999-03-02 2000-03-02 Corrosion inhibitor and process Abandoned CA2299857A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US26068499 true 1999-03-02 1999-03-02
US09/260,684 1999-03-02

Publications (1)

Publication Number Publication Date
CA2299857A1 true true CA2299857A1 (en) 2000-09-02

Family

ID=22990180

Family Applications (1)

Application Number Title Priority Date Filing Date
CA 2299857 Abandoned CA2299857A1 (en) 1999-03-02 2000-03-02 Corrosion inhibitor and process

Country Status (2)

Country Link
CA (1) CA2299857A1 (en)
WO (1) WO2000052230A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8071715B2 (en) 2007-01-31 2011-12-06 Georgia-Pacific Chemicals Llc Maleated and oxidized fatty acids
US8133970B2 (en) 2008-01-31 2012-03-13 Georgia-Pacific Chemicals Llc Oxidized and maleated derivative compositions
WO2014145972A3 (en) * 2013-03-15 2014-12-04 Ethox Chemicals, Llc Bio-based dispersants

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3450247B2 (en) * 1999-12-28 2003-09-22 Necエレクトロニクス株式会社 Metal wiring formation method

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0711850B1 (en) * 1994-11-08 1999-03-10 Betzdearborn Europe, Inc. Method using a water soluble cyclic amine-dicarboxylic acid-alkanol amine salt corrosion inhibitor
US5759485A (en) * 1997-05-12 1998-06-02 Westvaco Corporation Water soluble corrosion inhibitors

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8071715B2 (en) 2007-01-31 2011-12-06 Georgia-Pacific Chemicals Llc Maleated and oxidized fatty acids
US8334363B2 (en) 2007-01-31 2012-12-18 Georgia-Pacific Chemicals Llc Oxidized and maleated compounds and compositions
US8133970B2 (en) 2008-01-31 2012-03-13 Georgia-Pacific Chemicals Llc Oxidized and maleated derivative compositions
WO2014145972A3 (en) * 2013-03-15 2014-12-04 Ethox Chemicals, Llc Bio-based dispersants
CN105431511A (en) * 2013-03-15 2016-03-23 埃瑟克斯化学有限责任公司 Bio-Based Dispersants

Also Published As

Publication number Publication date Type
WO2000052230A1 (en) 2000-09-08 application

Similar Documents

Publication Publication Date Title
US3374171A (en) Aqueous lubricant compositions containing an alkanolamine, a saturated organic acid and a polyoxyalkylene glycol
US3429909A (en) Secondary aminoalcohol-boric acid reaction product and production thereof
US2999064A (en) Stable aqueous cutting fluid
US5062979A (en) Soap free conveyor lubricant that gives clear solutions in water comprising alkoxyphosphate ester, alkyl benzene sulfonate and carboxylic acid
US6525005B1 (en) Antimicrobial conveyor lubricant composition and method for using
US3317430A (en) Detergent compositions
US5614027A (en) Metal cleaner with novel anti-corrosion system
US4391722A (en) Water-based low foam hydraulic fluid employing 2-ethylhexanol defoamer
US6204225B1 (en) Water-dispersible metal working fluid
US4264479A (en) Surfactant system
US5935914A (en) Lubricants for conveyor belt installation in the food industry
US3931029A (en) Corrosion inhibited antifreeze compositions and process for inhibiting the corrosion of solder alloys
US6686325B2 (en) Alkaline sensitive metal cleaning composition, method for cleaning an alkaline sensitive metal surface, and washing facility
US5073280A (en) Composition for inhibiting stress cracks in plastic articles and methods of use therefor
US3496104A (en) Cold rolling agent
US3663445A (en) Surface cleaning and defatting composition
US6372698B1 (en) Lubricant for chain conveyor belts and its use
US5391308A (en) Lubricant for transport of P.E.T. containers
US4389371A (en) Process for inhibiting the corrosion of aluminum
US5744069A (en) Water soluable metal anticorrosive
US4212750A (en) Metal working lubricant
US4491526A (en) Thickened, water-based hydraulic fluid with reduced dependence of viscosity on temperature
US5132046A (en) Water-based metal working fluid containing at least one alkanolamine compound as antimicrobial agent and a metal working process performed in the presence of said fluid
US5935920A (en) Cleaner with high wetting power
US5723418A (en) Alkyl ether amine conveyor lubricants containing corrosion inhibitors

Legal Events

Date Code Title Description
FZDE Dead