US3801504A - Non-flammable water based hot forging lubricating compositions - Google Patents

Non-flammable water based hot forging lubricating compositions Download PDF

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US3801504A
US3801504A US00126892A US3801504DA US3801504A US 3801504 A US3801504 A US 3801504A US 00126892 A US00126892 A US 00126892A US 3801504D A US3801504D A US 3801504DA US 3801504 A US3801504 A US 3801504A
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water
hot forging
clay
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A Stone
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Texaco Inc
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    • 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
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    • 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
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    • 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
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/04Elements
    • C10M2201/041Carbon; Graphite; Carbon black
    • C10M2201/042Carbon; Graphite; Carbon black halogenated, i.e. graphite fluoride
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/06Metal compounds
    • C10M2201/062Oxides; Hydroxides; Carbonates or bicarbonates
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    • C10M2201/087Boron oxides, acids or salts
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/10Compounds containing silicon
    • C10M2201/102Silicates
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    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/10Compounds containing silicon
    • C10M2201/102Silicates
    • C10M2201/103Clays; Mica; Zeolites
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/086Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type polycarboxylic, e.g. maleic acid
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • 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
    • C10M2209/104Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/12Polysaccharides, e.g. cellulose, biopolymers
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    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/24Metal working without essential removal of material, e.g. forming, gorging, drawing, pressing, stamping, rolling or extruding; Punching metal
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/241Manufacturing joint-less pipes
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/242Hot working
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/243Cold working
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
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    • C10N2040/244Metal working of specific metals
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/245Soft metals, e.g. aluminum
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/246Iron or steel
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
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    • C10N2040/244Metal working of specific metals
    • C10N2040/247Stainless steel
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    • C10N2070/00Specific manufacturing methods for lubricant compositions
    • C10N2070/02Concentrating of additives

Definitions

  • This invention concerns non-flammable water-based metal working lubricants. More particularly, this invention relates to the above lubricants containing alkali metal metasilicates and borax, and which have improved characteristics over compositions of the prior art.
  • Forging is a process for increasing the density, toughness and strength of the metal by grain deformation. It can be performed while the metal is in the hot state or cold. Both processes have advantages and disadvantages. While cold forging upgrades metallurgical properties, hot forging requires the expenditure of less energy and permits greater deformation. Two primary factors which are especially important in hot forging operations are the rate of production and die life. The dies are very expensive and every precaution, including the choice of proper lubricants, is taken to extend die life. The use of lubricants is to minimize metal pick-up and wear. Improper lubrication can cause undesired metal slippage and can result in defective forgings.
  • non-clay thickeners such as sodium carboxymethylcellulose
  • Clay thickeners are selected from the group consisting of finely divided particles of the montmorillonite group of minerals. These are expanding lattice type minerals illustrated most commonly by bentonite and hectorite. The major difference between the former over thelatter is that bentonite contains alumina as a major constituent while hectorite contains magnesia as a major component. More specifically, bentonite is a sodium aluminum silicate, while hectorite is a sodium magnesium-fluoro-litho-silicate. Usually the particle size of these clays is between 0.05 mm. and 0.01 mm. in diameter and they have an effective specific surface of the order of 200 to 400 square meters per gram.
  • Hectorite having a specific area of the order of 300 to 350 square meters per gram and whose dimensions when dispersed in solution are approximately 1 millimicron by 700 millimicrons is the preferred clay thickener.
  • Non-clay thickeners are referred to as organic thickeners and include alkylcelluloses, polymethylvinyl ether-maleic anhydride, alkali metal alkylcelluloses, and mixtures of one or more of these organic thickeners can aso be used.
  • a combination of hectorite with sodium carboxymethylcellulose is the preferred thickening system when used in the ratio of about 6 parts by weight of hectorite to about 1 part by weight of sodium carboxymethylcellulose.
  • Hectorite is preferred as the clay thickener because of its ability to be utilized in smaller concentrations than the bentonites to obtain the same degree of gelation and also because it exhibits a greater stability in aqueous solution.
  • (C) Fillers -Finely divided graphite having an average particle size of less than 50 microns is preferred. Preferably the particle size will have a particle size of less than 25 microns and will have a low ash content (less than 2.5% by weight) when fired. A mixture of graphite ranging from about 16 to 29 parts per Weight per hundred parts by weight of the finished grease is the preferred concentration. A mixture of up to 5 parts by Weight of finely particulated calcium carbonate when used with 16 to 29 grease, in order to more easily calculate the relative proportions of the components present,
  • (D) Sunfactant The surfactants which have proven to be the most useful of the commercially available materials are those alkoxylated derivatives of alkylated phenols containing an average of from 2 to 30 moles of alkylene oxide in the molecule, and where the alkylating group or groups contain from 4 to 12 carbon atoms per molecule of phenol.
  • the favored surfactant is nonylphenol ethoxylated with an average of from about 2 to 30 ethoxylate molecules.
  • the preferred surfactant is nonylphenol contain-. ing an average of 9.5 moles of ethoxylate in the molecule.
  • the lubricants may be used as formulated or cut back by diluting with water.
  • water dilutions ranging from about 1 part by weight up to about parts by weight of water per part by wieght of concentrate can be employed.
  • about equi-weight ratios are preferred.
  • the non-flammable composition is a black, thixotropic semi-solid lubricant, designed to be diluted with Water up to a 1:1 dilution.
  • the 1:1 cutback is fluid enough to be pumped and sprayed, shows good hot metal properties and is non-corrosive to steel and forms a stable, nonsettling product.
  • Example 3 when the components of Example 3 are added in a slightly diiferent sequence, an unsatisfactory lubricant (not sufiiciently stiff) is produced.
  • the grease lacks the necessary stiifness even if the remaining components of sodium metasilicate, sodium carboxymethylcellulose, borax and calcium carbonate are previously prepared and added to the water dispersion of surfactant and clay.
  • the hot forging lubricants of this invention have several advantages over the known prior art.
  • it in its diluted form (1:1), it provides good uniform coverage of the hot metal and can be applied by either spraying, dipping or by other dispersing methods of the art. It fulfills its primary function of cooling the workpiece and die, as well as setting the hot metal parts.
  • the lubricant is non-flammable and minimizes air pollution.
  • a non-flammable, Water-based, thixotropic hot forging lubricant composition concentrate suitable for further dilution with water consisting essentially of the following admixture of components in the indicated proportions:
  • clay thickener selected from the group consisting of bentonite and hectorite clays having a particle size of between 0.05 mm. and 0.01 mm. in diameter and an effective specific surface area in the order of 200 to 400 square meters per gram of clay,
  • composition includes up to 0.5 part by weight of surfactant selected from the group consisting of alkoxylated alkyl phenols containing an average of from 2 to 30 moles of alkylene oxide in the molecule, and where the alkylating group contains from 4 to 12 carbon atoms per molecule of phenol.
  • surfactant selected from the group consisting of alkoxylated alkyl phenols containing an average of from 2 to 30 moles of alkylene oxide in the molecule, and where the alkylating group contains from 4 to 12 carbon atoms per molecule of phenol.
  • a water-based, non-flammable hot forging lubricant concentrate consisting essentially of the following components in the indicated proportions:
  • a hot forging water-based, non-flammable lubricant concentrate consisting essentially of the following components in the indicated proportions:
  • a hot forging water-based, non-flammable lubricant concentrate consisting essentially of the following components in the indicated proportions:
  • trate suitable for further dilution with water consisting essentially of the steps of admixing (a) from about one-quarter to two-thirds of the weight of water used in the finished water-based lubricant with from about 2.5 to 5.5 parts by weight of clay thickener selected from the group consisting of bentonite and hectorite clays having a particle size of between 0.05 mm. and 0.01 mm. and having an effective specific surface area in the order of 200 to 400 square meters per gram of clay, and from about 12 to 29 parts by weight of graphite until a homogenous admixture is formed, and

Abstract

LUBRICANT COMPOSITION COMPRISING: (A) WATER BASE, (B) CLAY THICKENER, (C) GRAPHITE, (D) BORAX, (E) SODIUM METASILICATE, (F) NON-CLAY THICKENER, (G) POLYALKOXYLATED ALKYPHENOLS.

Description

United States Patent ABSTRACT OF THE DISCLOSURE Lubricant composition comprising:
(a) water base,
(b) clay thickener,
(c) graphite,
(d) borax,
(e) sodium metasilicate,
(f) non-clay thickener,
(g) polyalkoxylated alkyphenols.
This invention concerns non-flammable water-based metal working lubricants. More particularly, this invention relates to the above lubricants containing alkali metal metasilicates and borax, and which have improved characteristics over compositions of the prior art.
BACKGROUND OF THE INVENTION The metal industry is frequently used as a bellweather of industrial development and the afiiuence of a country.
.Upon first blush this seems rather anomalous since most metals have relatively little intrinsic value until they have been worked. That is, it is only after the metal has been forged, molded or otherwise shaped into useful forms that the value of the original, unworked metal appreciates manyfold.
Forging is a process for increasing the density, toughness and strength of the metal by grain deformation. It can be performed while the metal is in the hot state or cold. Both processes have advantages and disadvantages. While cold forging upgrades metallurgical properties, hot forging requires the expenditure of less energy and permits greater deformation. Two primary factors which are especially important in hot forging operations are the rate of production and die life. The dies are very expensive and every precaution, including the choice of proper lubricants, is taken to extend die life. The use of lubricants is to minimize metal pick-up and wear. Improper lubrication can cause undesired metal slippage and can result in defective forgings.
" However, the primary requirements of lubricants, particularly in hot forging operations, is to cool down the temperature of the workpiece and die as well as to wet the hot metal and thereby minimize frictional etfects caused by the workpiece sliding over the die. Further requirements are to eliminate the hazards of fire and minimize air pollution. Inasmuch as the die temperatures during use can range from 300 F. to about 600 F., the
use of conventional soap thickened mineral oil-based caused or accelerated corrosion.
. In view of the problems encountered with both oilbased and water-based lubricants, a need exists to develop a water-based lubricant which, in addition to being nonflammable, has improved hot metal wetting characteristics and which minimizes or inhibits corrosion.
Therefore, it is an'object of this invention to provide Patented Apr. 2, 1974 water-based hot forging lubricant concentrates which have substantially improved wetting properties and which minimize or inhibit corrosion.
These objects, among many others, are achieved by the preparation of the improved non-flammable, hot forging composition where preparation is described below:
A portion of the water used in the finished hot forging concentrate, usually about one-quarter to two-thirds of the total water, is charged to an oil-free kettle or vessel of an appropriate size fitted with the usual heating, cooling and mixing means. All of the clay thickener is stirred into the kettle containing water until the clay is evenly dispersed. At the time all of the graphite used is added to the aqueous clay dispersion until a homogenous mixture is obtained. Ordinarily a previously and separately prepared aqueous gel comprising non-clay thickeners (such as sodium carboxymethylcellulose), borax and sodium metasilicate is added to the aqueous clay dispersion until a uniformly dispersed mixture is obtained. At this point, all of the surfactant is added with stirring followed by the addition of the remainder of the water which has been used as rinse of the separately prepared gel container. The black gelled mixture is stirred with circulation and put through a sieve of the desired pore size and stored for use.
The order of above blending procedure is critical to success in that varying the sequence of addition of the various components produces a lubricant possessing inferior stability.
(A) Clay thickeners.-The favored clay thickeners are selected from the group consisting of finely divided particles of the montmorillonite group of minerals. These are expanding lattice type minerals illustrated most commonly by bentonite and hectorite. The major difference between the former over thelatter is that bentonite contains alumina as a major constituent while hectorite contains magnesia as a major component. More specifically, bentonite is a sodium aluminum silicate, while hectorite is a sodium magnesium-fluoro-litho-silicate. Usually the particle size of these clays is between 0.05 mm. and 0.01 mm. in diameter and they have an effective specific surface of the order of 200 to 400 square meters per gram.
Hectorite having a specific area of the order of 300 to 350 square meters per gram and whose dimensions when dispersed in solution are approximately 1 millimicron by 700 millimicrons is the preferred clay thickener.
(B) Non-clay thickeners.These optional thickeners are referred to as organic thickeners and include alkylcelluloses, polymethylvinyl ether-maleic anhydride, alkali metal alkylcelluloses, and mixtures of one or more of these organic thickeners can aso be used.
A combination of hectorite with sodium carboxymethylcellulose is the preferred thickening system when used in the ratio of about 6 parts by weight of hectorite to about 1 part by weight of sodium carboxymethylcellulose. Hectorite is preferred as the clay thickener because of its ability to be utilized in smaller concentrations than the bentonites to obtain the same degree of gelation and also because it exhibits a greater stability in aqueous solution.
(C) Fillers.-Finely divided graphite having an average particle size of less than 50 microns is preferred. Preferably the particle size will have a particle size of less than 25 microns and will have a low ash content (less than 2.5% by weight) when fired. A mixture of graphite ranging from about 16 to 29 parts per Weight per hundred parts by weight of the finished grease is the preferred concentration. A mixture of up to 5 parts by Weight of finely particulated calcium carbonate when used with 16 to 29 grease, in order to more easily calculate the relative proportions of the components present,
parts by weight of graphite appears to improve the uniformity of the finished grease composition.
(D) Sunfactant.--The surfactants which have proven to be the most useful of the commercially available materials are those alkoxylated derivatives of alkylated phenols containing an average of from 2 to 30 moles of alkylene oxide in the molecule, and where the alkylating group or groups contain from 4 to 12 carbon atoms per molecule of phenol. The favored surfactant is nonylphenol ethoxylated with an average of from about 2 to 30 ethoxylate molecules. The preferred surfactant is nonylphenol contain-. ing an average of 9.5 moles of ethoxylate in the molecule.
(D) Dilution of concentrate-The lubricants may be used as formulated or cut back by diluting with water. Generally, water dilutions ranging from about 1 part by weight up to about parts by weight of water per part by wieght of concentrate can be employed. However, inasmuch as the stability of the diluted concentrates decrease when the weight ratio of water to concentrate exceeds 1: 1, about equi-weight ratios are preferred.
(E) Preferred compositions-The components of the inventive lubricants are present in the following proportions:
(1) Water-from about 60 to 75 parts by weight.
(2) Thickenerfrom about 2.5 to about 5.5 percent hectorite clay, including optionally from 0.0 to 1.0 part by weight of sodium carboxymethylcellulose.
(3) Filler-from about 12 to 29 parts by weight of graphite, including optional calcium carbonate.
(4) Surfactantfrom 0.0 to about 0.6 part by weight of a nonylphenol containing an average of 9.5 ethoxylate groups in the molecule.
(5) Borax-from about 0.75 to 2.0 parts by weight.
(6) Sodium metasilicate pentahydratefrom 1.5 to 6.5 parts by Weight.
(F) Testing.Three criteria are used to determine the suitability of a lubricant sample to perform under operational conditions. They are:
1) Ability to Wet oily metal.A 1:10 ratio of a naphthenic oil in water emulsion is applied to a small piece of clean boiler plate and allowed to dry. A thin coating of the hot forging compound in diluted aqueous form is applied over the oily metal either by spraying or using a fiber paint roller. After standing for 5 minutes, the plates are rated visually for uniformity of coating. Ratings were either excellent, good, fair or poor.
(2) Brake on test.A clean piece of boiler plate is coated on one side with a known amount of hot (forging compound and allowed to dry. The plate is then placed in a furnace at 1600-1800 F. for 6 minutes. After removal and cooling visual ratings as follows were used: (a) gooduniform residue, no peeling or cracking; (b) fair--cracking, no peeling; (c) poor--peeling and cracking of residue.
(3) Spray test.-A vertically suspended piece of boiler plate x 10" x A") is heated before three triangularly arranged Fisher burners. The hot forging lubricants are applied by spraying (300 p.s.i.g.) at the nozzle (0.019 inch diameter), and gave a 90 spray pattern from a nozzle distance of 8-10 inches by one sweep requiring 3-4 seconds. The cooled pieces of plate are examined for uniform coverage.
To illustrate the detailed workings of the invention, two preparations of hot forging lubricants are submitted. Unless otherwise noted, all parts or percentages are by weight and all temperatures are F. rather than C.
EXAMPLE 1 Preparation of an illustrative hot forging lubricating composition In this preparation the procedure as disclosed is used to give a composition as given below.
Component: Parts by weight Water 64.1 Hectorite clay 2.9
Nonylphenol ethoxylated with an average of 9.5 ethoxylate groups 0.4 Sodium metasilicate- SH O 4.0 Sodium carboxymethylcellulose 0.6 Borax (Na B O -10H O) 1.0 Graphite 27.0
The non-flammable composition is a black, thixotropic semi-solid lubricant, designed to be diluted with Water up to a 1:1 dilution. The 1:1 cutback is fluid enough to be pumped and sprayed, shows good hot metal properties and is non-corrosive to steel and forms a stable, nonsettling product.
EXAMPLE 2 Preparation of a slightly different hot forging lubricant Again the procedure as disclosed is employed to produce the product whose composition by weight is disclosed below.
Component: Parts by weight Water 71.5 Hectorite clay 2.9 Sodium metasilicate-5H O 2.0 Sodium carboxymethyl-cellulose 0.6 Borax (Na2B407' 1.0 Graphite 22.0
Preparation of another hot forging lubricant Once more the preparative procedure is employed to produce the product whose composition by weight is disclosed below.
Component: Parts by Weight Water 74.6 Hectorite clay 4.0
Nonylphenol ethoxylated with an average of 12 ethoxylate groups 0.4 Sodium metasilicate-5H O 3.0 Sodium carboxymethyl-cellulose 1.0 Borax (Na2B407' Graphite 13.0 Calcium carbonate 2.0
When the above lubricant concentrate is cut back 1:1 with water, a satisfactory hot forging lubricant having the desired properties is produced.
However, when the components of Example 3 are added in a slightly diiferent sequence, an unsatisfactory lubricant (not sufiiciently stiff) is produced.
For example, using the sample proportions and components above, if the addition of surfactant to the water is made before the clay is dispersed into the water system, the grease lacks the necessary stiifness even if the remaining components of sodium metasilicate, sodium carboxymethylcellulose, borax and calcium carbonate are previously prepared and added to the water dispersion of surfactant and clay.
As the preceding specification and examples have indicated, the hot forging lubricants of this invention have several advantages over the known prior art. For example, in its diluted form (1:1), it provides good uniform coverage of the hot metal and can be applied by either spraying, dipping or by other dispersing methods of the art. It fulfills its primary function of cooling the workpiece and die, as well as setting the hot metal parts. In addition, the lubricant is non-flammable and minimizes air pollution.
In addition to the above advantages, the novel invention is relatively flexible in that numerous substitutions, changes and modifications can be made without departing from the inventive concept.
The true metes and bounds of this invention can best be determined by a perusal of the following claims read in the light of this specification.
What is claimed is:
1. A non-flammable, Water-based, thixotropic hot forging lubricant composition concentrate suitable for further dilution with water consisting essentially of the following admixture of components in the indicated proportions:
(a) from about 60-75 parts by weight of water,
(b) from about 2.5-5.5 parts by weight of clay thickener selected from the group consisting of bentonite and hectorite clays having a particle size of between 0.05 mm. and 0.01 mm. in diameter and an effective specific surface area in the order of 200 to 400 square meters per gram of clay,
(c) from about 12-29 parts by weight graphite,
(d) from about 0.75-2.0 parts by weight borax,
(e) from about 1.5-6.5 parts by weight sodium metasilicate.
2. The lubricant of claim 1 wherein the composition includes up to 0.5 part by weight of surfactant selected from the group consisting of alkoxylated alkyl phenols containing an average of from 2 to 30 moles of alkylene oxide in the molecule, and where the alkylating group contains from 4 to 12 carbon atoms per molecule of phenol.
3. The lubricant of claim 2 wherein the surfactant is an ethoxylated nonylphenol.
4. The lubricant of claim 1 wherein up to 1.0 part by weight of sodium carboxymethylcellulose thickener is present in the hot forging lubricating composition.
5. A water-based, non-flammable hot forging lubricant concentrate consisting essentially of the following components in the indicated proportions:
6. A hot forging water-based, non-flammable lubricant concentrate consisting essentially of the following components in the indicated proportions:
Component: Parts by weight Water 71.5 Hectorite clay 2.9 Graphite 22.0 Sodium carboxymethylcellulose 0.6 Sodium metasilicate'5H O 2.0 Borax 1.0
7. A hot forging water-based, non-flammable lubricant concentrate consisting essentially of the following components in the indicated proportions:
trate suitable for further dilution with water consisting essentially of the steps of admixing (a) from about one-quarter to two-thirds of the weight of water used in the finished water-based lubricant with from about 2.5 to 5.5 parts by weight of clay thickener selected from the group consisting of bentonite and hectorite clays having a particle size of between 0.05 mm. and 0.01 mm. and having an effective specific surface area in the order of 200 to 400 square meters per gram of clay, and from about 12 to 29 parts by weight of graphite until a homogenous admixture is formed, and
. (b) admixing a previously prepared homogenous admixture comprising from about 0.0 to 1.0 part by Weight of sodium carboxymethylcellulose from about 1.5 to 6.5 parts by weight of sodium metasilicate pentahydrate and from about 0.75 to 2.0 parts by weight of borax with said clay-graphite-water mixture until a uniform dispersion is produced, and
(c) admixing said aqueous dispersion with from 00 to 0.5 part by weight of an ethoxylated alkylphenol surfactant and the residual 'water to prepare the desired homogenous, non-flammable, water-based, hot forging lubricant.
9. The process of claim 8 wherein the clay thickener is hectorite, the ethoxylated alkylphenol surfactant is a nonylphenol containing an average of 9.5 ethoxylate groups per molecule of nonylphenol.
References Cited UNITED STATES PATENTS 2,833,717 5/1958 Whitacre 252-33.4 2,735,814 2/1956 Hodson et al. 25230 2,711,394 6/ 1955 Veatch et al 252-30 2,588,625 3/1952 Ferner et a1. 252-30 3,384,581 5/ 1968 Peace 25230 2,258,202 10/1941 Burns 252-30 1,395,073 10/1921 Willey 252-30 1,249,249 12/ 1917 Thorswik 25230 FOREIGN PATENTS 583,905 9/1959 Canada 252-30 189,500 1/ 1966 U.S.S.R 252-30 DANIEL E. WYMAN, Primary Examiner I. VAUGHN, Assistant Examiner US. Cl. X.R.
US00126892A 1971-03-22 1971-03-22 Non-flammable water based hot forging lubricating compositions Expired - Lifetime US3801504A (en)

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Cited By (27)

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US4052323A (en) * 1974-05-08 1977-10-04 Lonza, Ltd. High-temperature lubricant for the hot-working of metals
DE2734906A1 (en) * 1976-08-04 1978-02-09 Singer & Hersch Industrial Dev AQUEOUS LIQUID OR CONCENTRATE, METHOD FOR THE PRODUCTION AND USE THEREOF
US4104178A (en) * 1975-10-24 1978-08-01 Wyman-Gordon Company Water-based forging lubricant
US4115282A (en) * 1975-12-02 1978-09-19 Deutsche Texaco Aktiengesellschaft Biodegradable grease composition
US4155859A (en) * 1978-01-19 1979-05-22 The Lubrizol Corporation Forging lubricants and method of use thereof
US4287073A (en) * 1975-10-24 1981-09-01 Wyman-Gordon Company Water-based forging lubricant
US4336147A (en) * 1980-03-24 1982-06-22 Chevron Research Company Borate-containing water-in-oil microemulsion fluid
US4337161A (en) * 1980-03-24 1982-06-29 Chevron Research Company Borate-containing oil-in-water microemulsion fluid
AT379682B (en) * 1984-09-17 1986-02-10 Forschungsgesellschaft Joanneu ABSORPTION REFRIGERATOR
US4808324A (en) * 1986-04-04 1989-02-28 Lonza Ltd. Lubricant system for sheet and section rolling mills
US4828730A (en) * 1986-07-18 1989-05-09 Cincinnati Milacron Inc. Alkali metal aluminum silicate containing metal working fluid compositions and processes for machining metal employing such compositions
US5016456A (en) * 1988-03-30 1991-05-21 Lonza Ltd. Process for making hollow billets into tubes
US5042209A (en) * 1988-01-19 1991-08-27 Lonza Ltd. Process for charging a carrier gas stream with a free-flowing material and process for operating the device
US5099667A (en) * 1989-06-16 1992-03-31 Lonza Ltd. System for suspending and applying solid lubricants to tools or work pieces
US5102468A (en) * 1987-09-29 1992-04-07 Lonza Ltd. Device for applying a descaling agent to the inner surface of a hollow billet
DE4129140A1 (en) * 1991-09-02 1993-03-04 Del Ross Sergio WAESSED METAL-PROCESSING FLUIDS FOR TASTE-CUTTING CUTTING WORK AND THEIR USE
US5205488A (en) * 1990-03-26 1993-04-27 Lonza Ltd. Process and device for spraying a liquid intermittently, especially a lubricant suspension to be sprayed under high pressure
EP0554822A1 (en) * 1992-02-06 1993-08-11 Lonza Ag Mandrel lubricant for the manufacture of seamless tubes
US5271854A (en) * 1986-09-23 1993-12-21 Lonza Ltd. High temperature lubricant containing carboxylated styrene-butadiene latex
WO1994013760A2 (en) * 1992-12-01 1994-06-23 A.W. Chesterton Company Malleable packing
US5691282A (en) * 1995-05-16 1997-11-25 Timcal Ltd. Lubricant composition for use on workpieces in the hot forming of metals
WO1998013445A1 (en) * 1996-09-25 1998-04-02 Kelsan Technologies Corp. Solid lubricants and friction modifiers for heavy loads and rail applications
EP1316603A1 (en) * 2000-08-11 2003-06-04 Henkel Kommanditgesellschaft auf Aktien Water-based composition for protective film formation
DE102004045128A1 (en) * 2004-09-17 2006-03-23 Chemische Fabrik Budenheim Kg Lubricant for lubricating heated metal objects
EP2061862A2 (en) * 2006-08-21 2009-05-27 Dmitry Tananko Method for composing a nano-particle metal treatment composition for creating a ceramic-metal layer
US20120282369A1 (en) * 2011-05-02 2012-11-08 Pandur Jozsef Method for increasing the nutritional value of rapeseed and rape products with decreased oil content
EP3124582A4 (en) * 2014-03-28 2017-12-13 Nihon Parkerizing Co., Ltd. Aqueous lubricating coating agent having excellent corrosion resistance and workability, and metal material

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4052323A (en) * 1974-05-08 1977-10-04 Lonza, Ltd. High-temperature lubricant for the hot-working of metals
US4104178A (en) * 1975-10-24 1978-08-01 Wyman-Gordon Company Water-based forging lubricant
US4287073A (en) * 1975-10-24 1981-09-01 Wyman-Gordon Company Water-based forging lubricant
US4115282A (en) * 1975-12-02 1978-09-19 Deutsche Texaco Aktiengesellschaft Biodegradable grease composition
DE2734906A1 (en) * 1976-08-04 1978-02-09 Singer & Hersch Industrial Dev AQUEOUS LIQUID OR CONCENTRATE, METHOD FOR THE PRODUCTION AND USE THEREOF
US4155859A (en) * 1978-01-19 1979-05-22 The Lubrizol Corporation Forging lubricants and method of use thereof
US4336147A (en) * 1980-03-24 1982-06-22 Chevron Research Company Borate-containing water-in-oil microemulsion fluid
US4337161A (en) * 1980-03-24 1982-06-29 Chevron Research Company Borate-containing oil-in-water microemulsion fluid
AT379682B (en) * 1984-09-17 1986-02-10 Forschungsgesellschaft Joanneu ABSORPTION REFRIGERATOR
US4808324A (en) * 1986-04-04 1989-02-28 Lonza Ltd. Lubricant system for sheet and section rolling mills
US4828730A (en) * 1986-07-18 1989-05-09 Cincinnati Milacron Inc. Alkali metal aluminum silicate containing metal working fluid compositions and processes for machining metal employing such compositions
US5271854A (en) * 1986-09-23 1993-12-21 Lonza Ltd. High temperature lubricant containing carboxylated styrene-butadiene latex
US5102468A (en) * 1987-09-29 1992-04-07 Lonza Ltd. Device for applying a descaling agent to the inner surface of a hollow billet
US5042209A (en) * 1988-01-19 1991-08-27 Lonza Ltd. Process for charging a carrier gas stream with a free-flowing material and process for operating the device
US5016456A (en) * 1988-03-30 1991-05-21 Lonza Ltd. Process for making hollow billets into tubes
US5099667A (en) * 1989-06-16 1992-03-31 Lonza Ltd. System for suspending and applying solid lubricants to tools or work pieces
US5205488A (en) * 1990-03-26 1993-04-27 Lonza Ltd. Process and device for spraying a liquid intermittently, especially a lubricant suspension to be sprayed under high pressure
DE4129140A1 (en) * 1991-09-02 1993-03-04 Del Ross Sergio WAESSED METAL-PROCESSING FLUIDS FOR TASTE-CUTTING CUTTING WORK AND THEIR USE
KR100270173B1 (en) * 1992-02-06 2000-11-01 제임스 뷴 Mandrel lubricant for production of seamliess tubemandrel lubricant for production of seamliess tubes s
EP0554822A1 (en) * 1992-02-06 1993-08-11 Lonza Ag Mandrel lubricant for the manufacture of seamless tubes
US5492639A (en) * 1992-02-06 1996-02-20 Lonza Ltd. Mandrel lubricant for the production of seamless tubes
WO1994013760A3 (en) * 1992-12-01 1994-11-10 Chesterton A W Co Malleable packing
WO1994013760A2 (en) * 1992-12-01 1994-06-23 A.W. Chesterton Company Malleable packing
US5691282A (en) * 1995-05-16 1997-11-25 Timcal Ltd. Lubricant composition for use on workpieces in the hot forming of metals
WO1998013445A1 (en) * 1996-09-25 1998-04-02 Kelsan Technologies Corp. Solid lubricants and friction modifiers for heavy loads and rail applications
US6136757A (en) * 1996-09-25 2000-10-24 Kelsan Technologies Corporation Solid lubricants and friction modifiers for heavy loads and rail applications
AU736427B2 (en) * 1996-09-25 2001-07-26 Kelsan Technologies Corp. Solid lubricants and friction modifiers for heavy loads and rail applications
JP2001501994A (en) * 1996-09-25 2001-02-13 ケルサン テクノロジーズ コーポレイション Solid lubricants and friction modifiers for high load and track applications
EP1316603A1 (en) * 2000-08-11 2003-06-04 Henkel Kommanditgesellschaft auf Aktien Water-based composition for protective film formation
EP1316603A4 (en) * 2000-08-11 2009-09-09 Henkel Ag & Co Kgaa Water-based composition for protective film formation
DE102004045128A1 (en) * 2004-09-17 2006-03-23 Chemische Fabrik Budenheim Kg Lubricant for lubricating heated metal objects
EP2061862A2 (en) * 2006-08-21 2009-05-27 Dmitry Tananko Method for composing a nano-particle metal treatment composition for creating a ceramic-metal layer
EP2061862A4 (en) * 2006-08-21 2011-06-08 Dmitry Tananko Method for composing a nano-particle metal treatment composition for creating a ceramic-metal layer
US20120282369A1 (en) * 2011-05-02 2012-11-08 Pandur Jozsef Method for increasing the nutritional value of rapeseed and rape products with decreased oil content
EP3124582A4 (en) * 2014-03-28 2017-12-13 Nihon Parkerizing Co., Ltd. Aqueous lubricating coating agent having excellent corrosion resistance and workability, and metal material

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