CA1073442A - Hot melt metal working lubricants - Google Patents

Hot melt metal working lubricants

Info

Publication number
CA1073442A
CA1073442A CA283,299A CA283299A CA1073442A CA 1073442 A CA1073442 A CA 1073442A CA 283299 A CA283299 A CA 283299A CA 1073442 A CA1073442 A CA 1073442A
Authority
CA
Canada
Prior art keywords
mixture
acid
ester
alcohol
composition
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
Application number
CA283,299A
Other languages
French (fr)
Inventor
Richard W. Jahnke
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.)
Lubrizol Corp
Original Assignee
Lubrizol Corp
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
Priority claimed from US05/766,642 external-priority patent/US4116872A/en
Application filed by Lubrizol Corp filed Critical Lubrizol Corp
Application granted granted Critical
Publication of CA1073442A publication Critical patent/CA1073442A/en
Expired legal-status Critical Current

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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
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    • C10N2040/20Metal working
    • C10N2040/244Metal 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
    • 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
    • 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
    • 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
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/244Metal working of specific metals
    • C10N2040/247Stainless 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
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/015Dispersions of solid lubricants
    • C10N2050/02Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
    • 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
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/04Aerosols
    • 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
    • C10N2060/00Chemical after-treatment of the constituents of the lubricating composition
    • C10N2060/04Oxidation, e.g. ozonisation

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  • Chemical & Material Sciences (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Inorganic Chemistry (AREA)
  • Lubricants (AREA)
  • Forging (AREA)

Abstract

Title: HOT MELT METAL WORKING LUBRICANTS

Inventor: Richard William Jahnke Abstract of the Disclosure:
Metal working operations, especially drawing, are facilitated by applying to the metal a composition which provides lubricity thereto and which melts within the range of about 30-100°C. The composition comprises at least one neutral ester, and preferably a mixture of esters, prepared from polyalkylene glycols and saturated aliphatic alcohols having at least about 10 carbon atoms, and C12-25 aliphatic monocarboxylic acids and C4-20 aliphatic polycarboxylic acids. The preferred ester mixtures are prepared from poly-ethylene glycols, C14 -20 predominantly straight chain alkanols, stearic acid and adipic, azelaic or sebacic acid.
Optional ingredients include phosphorus acid salts and anti-oxidants. The composition may be applied in liquid form and solidifies on cooling to normal ambient and storage temperatures.

Description

This invention relates to metal working operations.
More particularly, it relates to compositions useful as lubricants and methods for lubricating metal during such ~ -operations, and to metal workpieces so lubricated.
Metal working operations, for example, rolling, forging, hot-pressing, blanking, bending, stamping, drawing, cutting, punching, spinning and the like generally employ a lubricant to facilitate the same. Lubricants greatly improve these operations in that they can reduce the power required for the operation, prevent sticking and decrease wear of dies, cutting bits and the like. In addition, they frequently provide rust inhibiting properties to the metal being treated.
Since it is conventional to subject the metal to ~ -various chemical treatments (such as the application of conversion coating solutions) after working, a cleaning operation is necessary between the working step and the chemical treatment step. In addition to the above proper-ties, therefore, it is preferred that the working lubricant be easily removable from the metal surface by ordinary cleaning compositions.
Heretofore, the lubricants applied for the above purposes have ordinarily been liquids. The equipment used for the application of such liquids is often expensive to ;
maintain and inconvenient to use. In addition, a dry-off oven is usually required to remove the water or solvent carrier from the liquid composition, which also greatly adds to the capital costs and operating and maintenance expenses of the method. Difficulties are also often encountered in automatic feeding of metal blanks and other-~ '-1-~, . ~ , . ., . ~ ::

wise handling the metal because the liquid compositions which are normally applied to the metal make it wet and slippery and consequently difficult to handle.
A principal object of the present invention, there-fore, is to provide an improved metal working method.
A further object is to provide a method using lubricants which impart to the metal being worked a unique combination of properties including lubricity, corrosion resistance, extreme pressure properties and protection against wear of working parts, and which in addition are relatively easy to remove from the surface of the metal by cleaning after the working operation is completed.
A further object is to provide novel compositions for use in the improved method.
Other objects will in part be obvious and will in part appear hereinafter.
According to this invention, the above objects are fulfilled by applying to the metal to be worked a composi-tion which provides lubricity thereto, which melts within the range of about 30-100C., and which comprises at least one neutral ester defined as follows:
I. The alcohol moieties are derived from (A) a polyalkylene glycol containing about 20-50 polyoxyalkylene units, or a mixture thereof with (B) at least one saturated aliphatic alcohol having at least about 10 carbon atoms;
II. The acid moieties are derived from (C) at least one Cl 2-2 5 aliphatic monocarboxylic acid, or a mixture thereof with (D) at least one C4-20 aliphatic polycarboxylic acid.

. .

~07344Z

Preferably, the composition melts to form a readily flowable liquid which is capable of easy and efficient application to the metal surface. One advantage of such a composition (sometimes referred to hereinafter as the "hot melt composi-tion") is that metals coated therewith are easier to handle under normal storage conditions than metals coated with pre-viously known lubricants.
The principal necessary characteristic of the hot melt composition is its capability of providing lubricity to the metal surface. For this purpose, lubricity may be de-fined in many ways which are well known to those s~illed in the art, and in terms of a number of test methods which, in one way or another, simulate metal working operations. For the purpose of this invention, a composition is deemed to provide lubricity to a metal workpiece if its use results in a deviation of 100 foot-pounds or less when tested by the following method:
A cold-rolled steel strip, 2" x 13-1/2", is drawn between two dies in an Instron Universal Tester, Model TT-C.
Prior to drawing, the edges of the strip are deburred and the strip is vapor degreased and wiped with a clean cloth.
It is then coated uniformly with a drawing lubricant and mounted in the testing machine. The dies are tightened by means of a torque wrench set at 40 foot-pounds torque and the strip is pulled through the die for two inches at the rate of five inches per minute. The force or "load", in foot-pounds, required to pull the strip through the die, and the deviation from a uniform load, are recorded on a chart.
The hot melt composition melts in the range of 30-100C., as previously indicated. Thus, it is solid at -normal ambient temperature (e.g., about 20-30C.) and pressure.
The preferred melting range is 35-70C., with 38-55C. being particularly desirable. When melted, the composition pre-ferably forms a readily flowable liquid.
The principal ingredient of the hot melt composi-tion is at least one substantially neutral ester (i.e., one in which substantially all of the acid groups are esterified) as defined hereinabove. The alcohols and acids from which the ester is derived are more fully identified as follows:
Alcohol A is a polyalkylene glycol, usually a polyethylene or polypropylene glycol and preferably the former, containing about 20-50 polyalkylene units. Such polyalkylene glycols are normally available as commercial mixtures such as the "Carbowax" polyethylene glycols sold by Union Carbide.
Alcohol B is at least one saturated aliphatic alcohol having at least about 10 carbon atoms. Examples are decanol, dodecanol, tetradecanol, stearyl alcohol, eicosanol, and commercial mixtures of such alcohols, as well as corresponding diols, triols, etc. Preferred are Cl 4-2 o alcohols, especially alkanols (that is, saturated monohydroxy alcohols) and more especially predominantly straight-chain alkanols.
Acid C is at least one C~ 2-2 5 aliphatic monocar-boxylic acid such as lauric, myristic, palmitic, stearic,eicosanoic, oleic or linoleic acid. Mixtures of such acids are also suitable. The preferred acid is stearic acid.
Acid D is at least one C4-20 aliphatic polycar-boxylic acid; examples are maleic, fumaric, succinic, adipic, glutaric, pimelic, sebacic, azelaic, suberic and citric 3~ ~,toe ~"

acids, as well as mixtures thereof. The preferred poly- -carboxylic acids are dicarboxylic and especially adipic, azelaic and sebacic acids.
A number of esters and ester mixtures are suitable for use according to this invention. For example, esters of alcohol A and acid C are useful; an example is the mono-stearate of a polyethylene glycol containing an average of about 22-48 oxyethylene units per molecule. The preferred ester compositions, however, contain a plurality of alcohol and acid moieties. Thus, they may comprise a mixture of at least one ester of alcohol A and acid C and at least one ester of alcohol B and acid D, typically containing about 5-95% by weight of the latter.
Especially preferred are mixtures of neutral esters of alcohols A and B and acids C and D, and compositions comprising such mixtures are within the scope of this inven-tion. They are conveniently prepared by simply reacting the alcohol mixture with the acid mixture, typically in the presence of a strong acid as catalyst. Most often, the alcohol mixture contains about 2-4 equivalents of A per equivalent of B and the acid mixture contains about 2-4 equivalents of C per equivalent of D. (The equivalent weight of an alcohol, for the purposes of this invention, is its molecular weight divided by the number of hydroxy groups per molecule and may be determined analytically, especially for polyalkylene glycols. The equivalent weight of a carboxylic acid is its molecular weight divided by the number of carboxy groups per molecule.) The preferred hot melt compositions contain, in addition to the esters described hereinabove, at least one ~073442 agent to improve extreme pressure properties. The most suitable extreme pressure agents are phosphorus acid salts of the formula ) a ~ !I x 4 M
R2(X2)b -5 wherein M is a Group I metal, a Group II metal, aluminum, tin, cobalt, lead, molybdenum, manganese, nickel or ammon-ium; each of Rl and R2 is a hydrocarbon-based radical, each of Xl, X2, X3 and X4 iS oxygen or sulfur; and each of a and b is 0 or 1.
In the above formula, each of Rl and R2 is a hydro-carbon-based radical. As used herein, the term "hydrocarbon-based radical" denotes a radical having predominantly hydro-carbon character within the context of this invention. Such radicals include the following:
(1) Hydrocarbon radicals, which may be aliphatic (e.g., alkyl or alkenyl), alicyclic (e.g., cycloalkyl or cycloalkenyl), aromatic, aliphatic- and alicyclic-substituted aromatic, aromatic-substituted aliphatic and alicyclic, and the like.
(2) Substituted hydrocarbon radicals, that is, radicals containing non-hydrocarbon substituents which, in ~ --~
the context of this invention, do not alter the predominantly hydrocarbon character of the radical. Suitable substituents of this type will be apparent to those skilled in the art.
(3) Hetero radicals; that is, radicals which, while predominantly hydrocarbon in character within the context of this invention, contain atoms other than carbon present in a chain or ring otherwise composed of carbon atoms. Suitable hetero atoms will be apparent to those skilled in the art and include, for example, nitrogen, oxygen and sulfur.
In general, no more than about three substituents or hetero atoms, and preferably no more than one, will be present for each 10 carbon atoms in the hydrocarbon-based -radical.
The hydrocarbon-based radicals in the phosphorus acid salt are ordinarily free from acetylenic and usually also from ethylenic unsaturation and have no more than about 30 carbon atoms, desirably no more than about 12 carbon atoms. They are usually hydrocarbon radicals such as methyl, ethyl, propyl, butyl, amyl, hexyl, octyl, decyl, dodecyl, vinyl, decenyl, cyclohexyl, phenyl and the like, all isomers 15 thereof being included. A particular preference is expressed `
for compounds in which Rl and R2 are lower alkyl radicals, the word "lower" denoting a radical containing not more than 7 carbon atoms.
It will be apparent that the phosphorus acids from 20 which the salts are derived include dialkylphosphoric acids, -~
dialkylphosphinic acids, and thio derivatives of such acids.
Preferred are the salts in which X3 and X4 are each sulfur and especially salts of phosphorodithioic acids; that is !
salts in which a and b are each 1 and Xl and x2 are each oxygen. In the above-defined salts, M may be any of the metals previously enumerated or ammonium; the latter term includes substituted ammonium salts (i.e., amine salts).
M is preferably zinc or lead, especially zinc.
The hot melt composition most often contains up to about 25% of the phosphorus acid salt as an optional ingredi-ent. It is also within the scope of this invention to incor-porate other known additives in minor amounts (typically about 0.01-5.0% by weight) into the hot melt composition. Es-pecially preferred other additives are antioxidants, typi-cally hindered phenols; such materials are well known in theart. Other suitable additives useful in these proportions include:
Surfactants, usually nonionic surfactants such as oxyalkylated phenols and the like.
Auxiliary extreme pressure agents such as chlori-nated waxes, sulfurized hydrocarbons, sulfurized esters, etc.
Corrosion and wear inhibiting agents, and auxiliary rust inhibiting agents.
Friction modifying agents, of which the following are illustrative: Alkyl or alkenyl phosphates of phosphites in which the alkyl or alkenyl group contains about 10-40 carbon atoms, and metal salts thereof, especially zinc salts;
Cl0-20 fatty acid amides; C,0-20 alkyl amine/s, especially tallow amines, and ethoxylated derivatives thereof; salts of 20 such amines with acids such as boric acid or phosphoric ~ -acid which have been partially esterified as noted above;
Cl 0-2 0,alkyl-substituted imidazolines and similar nitrogen heterocycles; sulfurized derivatives of sperm oil and other fatty oils; basic barium or calcium salts of such oils or of amine-formaldehyde condensates, especially those derived from tallow amines such as described above; and gels derived from basic alkaline earth metal sulfonates.
Melting point modifiers, typically relatively low melting point esters such as dioctyl phthalate.
The invention also contemplates the use of hot melt 1~7344Z

lubricants containing waxes and waxy polymers, such as crystal-line (including microcrystalline) and non-crystalline hydro-carbon waxes, hydroxylated hydrocarbon waxes, petrolatum, and low molecular weight olefin polymers, especially the poly-ethylenes sold as "Bareco Polywaxes" by Petrolite Corporation.Such waxes or polymers are typically present in amounts of about 0.25-1.0 part by weight per part of ester.
The hot melt composition may be prepared by in-timately blending the ingredients thereof, preferably in the liquid state, if more than one ingredient is involved. It may sometimes be preferable to employ a substantially inert liquid diluent to insure intimate blending. By "substantially inert" is meant a diluent which does not undergo any appre-ciable reaction with the ingredients of the composition under the conditions of blending. Preferred as diluents are liquids which are solvents for the ingredients being blended; suitable solvents will be apparent to those skilled in the art and pre-ferably comprise non-polar liquids such as benzene, toluene, xylene, chlorobenzene and the like. After blending is com-plete, the diluent is preferably removed, typically by evapora-tion.
It is also within the scope of the invention to incorporate a small particle size, pigment-type particulate solid in the hot melt lubricant to increase lubricity at temperatures above the melting point thereof. Suitable in this respect are such pigments as rutile titanium dioxide, anatase titanium dioxide, zinc oxide, leaded zinc oxide, zinc sulfide, lead titanate, antimony oxide, zirconium oxide, white lead, basic lead silicate, lithopone, titanated lithopone, titanium-barium pigment, titanium-calcium pigment, ~ T~ _g_ titanium-magnesium pigment, calcium carbonate, gilders whiting talc, barytes, magnesium silicate, aluminum silicates, diatomaceous earth, china clay, Asbestine, silica and mica.
Calcium carbonate is especially preferred. The amount of such pigment is typically about 0.1-0.2 part by weight per part of ester.
In the following table are listed typical hot melt compositions suitable for use in the method of this invention.

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Any metal to be worked may be treated according to the mèthod of this invention; examples are ferrous metals, aluminum, copper, magnesium, titanium, zinc and manganese as well as alloys thereof and alloys containing other ele-ments such as silicon.
The method of this invention includes any methodby which a metal workpiece may be coated with the hot melt composition prior to or concurrently with the working operation. For example, a cutting blade or drawing die may be coated with the composition which is then transferred to the workpiece by contact. More usually, however, the work-piece is coated with the hot melt composition before the -~
working operation. Thus, this invention also contemplates a metal workpiece having on its surface a film of the hot melt composition, whether in solid or liquid form. The hot melt composition will ordinarily form a continuous film over the entire surface of the workpiece. However, it is also within the scope of this invention to form a film on less than the entire surface of the workpiece. ~ -The physical state of the hot melt composition during application to the metal surface is not critical.
Thus, it may be applied as a solid (as by rubbing) or as a liquid (as by brushing, spraying, dipping, flooding, roller coating, reverse roller coating or the like). For ease and convenience of application, it is preferably applied in the liquid state, and when this is done the metal may be subse-quently cooled whereupon the hot melt composition solidifies, or it may be passed directly to the metal working operation while the composition is in the liquid state. Onelof the advantages of this invention, however, is that the hot melt composition solidifies to form a solid, non-blocking, non-slippery film on the metal workpiece, thus permitting con- i !
venient and safe material handling at reduced cost.
The surface temperature of the metal at the time - -the hot melt composition is applied may vary, for example, from normal ambient temperature to just below the decomposi-tion temperature thereof. Factors which will influence or determine the temperature of the metal at the time the composition is applied include processes which the metal is subjected to prior or subsequent to application of the composition, the melting point of the composition, and the temperature thereof at the time of application. Using the hot melt compositions described hereinabove, metal surface ~-temperatures of about 20-125C. at the time of application have been found particularly useful. The temperature of the hot melt composition should be higher than its melting temperature (preferably at least 10C. higher and usually about 20-40C. higher) at the time of application for ease of flow and uniform dispersion of the composition onto the metal and coverage thereby.
The melted hot melt composition may be applied to the metal in a minimum of space utilizing existing equipment such as coilers used in steel mills prior to coiling, and because it quickly solidifies at ambient temperatures and becomes dry, non-blocking and relatively non-slippery, standard handling equipment such as lifting and feeding rollers. Stackers and so on may also be used. The use of the hot melt composition also eliminates the need for a dry-off oven since there is no water or solvent to remove.

. .
. -;:

Claims (45)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE PROPERTY
OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A method for lubricating metal during working thereof which comprises applying to said metal a lubricating composition which provides lubricity thereto, said composi-tion melting within the range of about 30-100°C. and compris-ing at least one substantially neutral ester defined as follows:
I. The alcohol moieties are derived from (A) a polyalkylene glycol containing about 20-50 polyoxyalkylene units, or a mixture thereof with (B) at least one saturated aliphatic alcohol having at least about 10 carbon atoms;
II. The acid moieties are derived from (C) at least one C12-25 aliphatic monocarboxylic acid, or a mixture thereof with (D) at least one C4-20 aliphatic polycarboxylic acid.
2. A method according to claim 1 wherein the lubricating composition melts within the range of about 35-70°C.
3. A method according to claim 2 wherein the ester is at least one ester of alcohol A and acid C.
4. A method according to claim 2 wherein the ester is a mixture of at least one ester of alcohol A and acid C and at least one ester of alcohol B and acid D, the latter ester comprising about 5-95% by weight of said mixture.
5. A method according to claim 4 wherein A is a polyethylene glycol containing an average of 22-48 oxy-ethylene units, B is a C14-20 predominantly straight-chain alkanol or commercial mixture of such alkanols, C is an alkanoic acid and D is at least one of adipic, azelaic and sebacic acids.
6. A method according to claim 5 wherein C
is stearic acid.
7. A method according to claim 6 wherein the working comprises drawing.
8. A method according to claim 2 wherein the ester is a mixture prepared by reacting a mixture of alcohols A and B with a mixture of acids C and D.
9. A method according to claim 8 wherein about 2-4 equivalents of A are present per equivalent of B in the alcohol mixture, and about 2-4 equivalents of C are present per equivalent of D in the acid mixture.
10. A method according to claim 9 wherein A is a polyethylene glycol containing an average of 22-48 oxy-ethylene units, B is a C14-20 predominantly straight-chain alkanol or commercial mixture of such alkanols, C is an alkanoic acid and D is at least one of adipic, azelaic and sebacic acids.
11. A method according to claim 10 wherein C is stearic acid.
12. A method according to claim 11 wherein the working comprises drawing.
13. A method according to claim 2 wherein the composition additionally contains a phosphorus acid salt having the formula wherein M is a Group I metal, a Group II metal, aluminum, tin, cobalt, lead, molybdenum, manganese, nickel or ammonium;
each of R1 and R2 is a hydrocarbon-based radical; each of X1, X2, X3 and X4 is oxygen or sulfur; and each of a and b is 0 or 1.
14. A method according to claim 13 wherein M is zinc; each of R1 and R2 is a lower alkyl radical; X1 and X2 are oxygen; X3 and X4 are sulfur; and a and b are each 1.
15. A method according to claim 14 wherein the working comprises drawing.
16. A metal workpiece having on the surface thereof a film of a lubricating composition which provides lubricity thereto and which melts within the range of about 30-100°C., said composition comprising at least one substantially neutral ester defined as follows:
I. The alcohol moieties are derived from (A) a polyalkylene glycol containing about 20-50 polyoxyalkylene units, or a mixture thereof with (B) at least one saturated aliphatic alcohol having at least about 10 carbon atoms;
II. The acid moieties are derived from (C) at least one C12-25 aliphatic monocarboxylic acid, or a mixture thereof with (D) at least one C4-20 aliphatic polycarboxylic acid.
17. A workpiece according to claim 16 wherein the lubricating composition melts within the range of about 35-70°C.
18. A workpiece according to claim 17 wherein the ester is at least one ester of alcohol A and acid C.
19. A workpiece according to claim 17 wherein the ester is a mixture of at least one ester of alcohol A
and acid C and at least one ester of alcohol B and acid D, the latter ester comprising about 5-95% by weight of said mixture.
20. A workpiece according to claim 19 wherein A is a polyethylene glycol containing an average of 22-48 oxyethylene units, B is a C14-20 predominantly straight-chain alkanol or commercial mixture of such alkanols, C is an alkanoic acid and D is at least one of adipic, azelaic and sebacic acids.
21. A workpiece according to claim 20 wherein C
is stearic acid.
22. A workpiece according to claim 17 wherein the ester is a mixture prepared by reacting a mixture of alcohols A and B with a mixture of acids C and D.
23. A workpiece according to claim 22 wherein about 2-4 equivalents of A are present per equivalent of B
in the alcohol mixture, and about 2-4 equivalents of C are present per equivalent of D in the acid mixture.
24. A workpiece according to claim 23 wherein A is a polyethylene glycol containing an average of 22-48 oxyethylene units, B is a C14-20 predominantly straight-chain alkanol or commercial mixture of such alkanols, C is an alkanoic acid and D is at least one of adipic, azelaic and sebacic acids.
25. A workpiece according to claim 24 wherein C
is stearic acid.
26. A workpiece according to claim 17 wherein the composition additionally contains a phosphorus acid salt having the formula wherein M is a Group I metal, a Group II metal, aluminum, tin, cobalt, lead, molybdenum, manganese, nickel or ammonium;
each of R1 and R2 is a hydrocarbon-based radical; each of X1, X2, X3 and X4 is oxygen or sulfur; and each of a and b is 0 or 1.
27. A workpiece according to claim 26 wherein M is zinc; each of R1 and R2 is a lower alkyl radical; X1 and X2 are oxygen; X3 and X4 are sulfur; and a and b are each 1.
28. A composition which melts within the range of about 30-100°C. and which provides lubricity to metal surfaces, said composition comprising a mixture of sub-stantially neutral esters defined as follows:

I. The alcohol moieties are derived from (A) a polyalkylene glycol containing about 20-50 polyoxyalkylene units and (B) at least one saturated aliphatic alcohol having at least about 10 carbon atoms;
II. The acid moieties are derived from (C) at least one C12-25 aliphatic monocarboxylic acid and (D) at least one C4-20 aliphatic polycarboxylic acid.
29. A composition according to claim 28 which melts within the range of about 35-70°C.
30. A composition according to claim 29 wherein the ester is a mixture of at least one ester of alcohol A
and acid C and at least one ester of alcohol B and acid D, the latter ester comprising about 5-95% by weight of said mixture.
31. A composition according to claim 30 wherein A is a polyethylene glycol containing an average of 22-48 oxyethylene units, B is a C14-20 predominantly straight-chain alkanol or commercial mixture of such alkanols, C is an alkanoic acid and D is at least one of adipic, azelaic and sebacic acids.
32. A composition according to claim 31 wherein C is stearic acid.
33. A composition according to claim 29 wherein the ester is a mixture prepared by reacting a mixture of alcohols A and B with a mixture of acids C and D.
34. A composition according to claim 33 wherein about 2-4 equivalents of A are present per equivalent of B
in the alcohol mixture, and about 2-4 equivalents of C are present per equivalent of D in the acid mixture.
35. A composition according to claim 34 wherein A is a polyethylene glycol containing an average of 22-48 oxyethylene units, B is a C14-20 predominantly straight-chain alkanol or commercial mixture of such alkanols, C is an alkanoic acid and D is at least one of adipic, azelaic and sebacic acids.
36. A composition according to claim 35 wherein C is stearic acid.
37. A composition according to claim 28 which additionally contains at least one phosphorus acid salt having the formula wherein M is a Group I metal, a Group II metal, aluminum, tin, cobalt, lead, molybdenum, manganese, nickel or ammonium;
each of R1 and R2 is a hydrocarbon-based radical; each of X1, X2, X3 and X4 is oxygen or sulfur; and each of a and b is 0 or 1.
38. A composition according to claim 37 wherein M is zinc; each of R1 and R2 is a lower alkyl radical; X1 and X2 are oxygen; X3 and X4 are sulfur; and a and b are each 1.
39. A composition according to claim 28 which additionally contains an antioxidant.
40. A composition according to claim 30 which additionally contains an antioxidant.
41. A composition according to claim 32 which additionally contains an antioxidant.
42. A composition according to claim 33 which additionally contains an antioxidant.
43. A composition according to claim 35 which additionally contains an antioxidant.
44. A composition according to claim 36 which additionally contains an antioxidant.
45. A composition according to claim 38 which additionally contains an antioxidant.
CA283,299A 1976-10-27 1977-07-21 Hot melt metal working lubricants Expired CA1073442A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US73106076A 1976-10-27 1976-10-27
US05/766,642 US4116872A (en) 1977-02-08 1977-02-08 Hot melt metal working lubricants

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CA1073442A true CA1073442A (en) 1980-03-11

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ID=27112161

Family Applications (1)

Application Number Title Priority Date Filing Date
CA283,299A Expired CA1073442A (en) 1976-10-27 1977-07-21 Hot melt metal working lubricants

Country Status (10)

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JP (1) JPS5354159A (en)
BR (1) BR7705273A (en)
CA (1) CA1073442A (en)
DE (1) DE2748319A1 (en)
ES (1) ES462500A1 (en)
FR (1) FR2369336A2 (en)
GB (2) GB1551494A (en)
IT (1) IT1103297B (en)
MX (1) MX147444A (en)
SE (1) SE431767B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4172802A (en) * 1978-05-30 1979-10-30 Cincinnati Milacron Inc. Aqueous metal working fluid containing carboxylic acid group terminated diesters of polyoxyalkylene diols
JPS572397A (en) * 1980-06-05 1982-01-07 Daido Kagaku Kogyo Kk Lubricant for aluminum processing
DE3247426A1 (en) * 1982-12-22 1984-06-28 Merck Patent Gmbh, 6100 Darmstadt CUTTING OIL FOR THE BARBING PROCESSING OF COLORED METALS
FR2913355B1 (en) * 2007-03-08 2009-08-21 Michelin Soc Tech PROCESS FOR WET TREADING WIRE OF STEEL WIRES FOR REINFORCING PNEUMATIC BANDAGES
FR2913356B1 (en) * 2007-03-08 2009-08-14 Rhodia Recherches & Tech LUBRICATION WITH DISPERSIONS IN METAL DEFORMATION PROCESSES
JP7316883B2 (en) * 2019-08-30 2023-07-28 日本パーカライジング株式会社 Cold rolling oil composition and method for producing rolled steel sheet using the same

Also Published As

Publication number Publication date
ES462500A1 (en) 1978-12-16
BR7705273A (en) 1978-05-30
DE2748319A1 (en) 1978-05-03
GB1551493A (en) 1979-08-30
FR2369336A2 (en) 1978-05-26
IT1103297B (en) 1985-10-14
SE7708116L (en) 1978-04-28
MX147444A (en) 1982-12-03
GB1551494A (en) 1979-08-30
JPS5354159A (en) 1978-05-17
SE431767B (en) 1984-02-27

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