Method for working or forming metals in the presence of aqueous lubricants based on methanesulfonic acid

Abstract
A method for working or forming metals which consists in usings an aqueous lubricant containing as water-soluble extreme pressure additive, methanesulphonic acid or water-soluble methanesulphonic acid salt. The water-soluble methane sulphonic acid salt is an alkali or alkaline-earth, ammonium, alkanol amine or ethoxylated fatty amine salt. The inventive aqueous lubricants have good extreme pressure properties and good properties with respect to corrosion.
Description
FIELD OF THE INVENTION

The present invention relates to the field of lubricants and more particularly to that of aqueous lubricants containing water-soluble extreme pressure additives, and which are used for working or forming metals.


BACKGROUND

Metal working or forming operations require the use of a lubricant in order to reduce the forces between the part to be worked and the tool, to remove the chips and fragments, to cool the part or the plate worked, and to control its surface texture. Oil-based lubricants have conventionally been used. These are whole oils or emulsions to which lubricity promoters, antiwear (AW) and/or extreme pressure (EP) additives may have been added. EP additives are generally compounds containing sulfur. At the high temperatures prevailing at the contact between the metal parts during metal working operations, the sulfur compounds decompose. A layer of iron sulfide is formed on the surface of the parts, hindering the processes of welding and adhesion.


Whole oils have excellent lubricating properties, but when production rates are high, the removal of the heat generated requires the use of emulsions. However, the use of emulsions also tends to be limited because, over time, they deteriorate and give off foul odors. This is why the use of aqueous fluids is steadily spreading. These are either synthetic fluids, which are aqueous solutions based on water-soluble additives, or semisynthetic fluids which are oil-in-water microemulsions containing a large quantity of emulsifiers. However, while the aqueous fluids effectively remove the heat and display improved resistance to bacterial proliferation, they are often limited to metal working operations in which the friction and wear conditions are not too severe. This is because EP additives have been developed specifically for oils, so that very few of these additives are water-soluble and therefore suitable for aqueous fluids.


While numerous oil-soluble EP additives are available, the number of water-soluble EP additives is much smaller. In Lub. Eng. 1977, 3(6), 291-298, R. W. Mould et al. describe the EP properties of a number of water-soluble sulfur-bearing additives, such as sodium salts of thiosalicylic, 2-mercaptopropionic, 2,2′-dithiodibenzoic, 2,2′-dithiodipropionic and dithiodiglycolic acids. Similarly, the use of water-soluble salts of 3,3′-dithiodipropionic acid has been the subject of U.S. Pat. No. 4,880,552 and JP 63 265 997. In U.S. Pat. No. 4,606,833, dithiodiglycol is used in combination with a derivative of polyoxyalkylene glycol to improve the extreme pressure properties of aqueous lubricants. The use of derivatives of aminosulfonic acids as additives in aqueous lubricating systems has been the subject of patent application WO 8602941. More recently, in Japanese patent application JP 10 110 181, the water-soluble salts of 3,3′-dithiodipropionic acid were combined with alkyl thioacids in aqueous drawing and stamping lubricants.


However, these products are not sufficiently stable in water. They promote bacterial proliferation and liberate hydrogen sulfide, causing the aqueous fluids to emit a strong odor. Their formulation thus requires the use of a large quantity of bactericides, which is incompatible with the quantities usually permitted in aqueous lubricants. Furthermore, some of these extreme pressure additives are incompatible with most of the other additives routinely used in synthetic and semisynthetic formulations.


Recently, lubricant compositions containing salts of sulfamic acid amines with extreme pressure effect have been the subject of patent application WO 00/44848. However, sulfamic acid is highly corrosive. Moreover, its low solubility precludes the production of liquid concentrates that are easy to use in the formulations. Furthermore, to limit the environmental impact of the lubricant formulations used in the field of metal working and forming, it is particularly important to employ readily biodegradable additives.


SUMMARY OF THE INVENTION

It has now been found that the use of methanesulfonic acid (MSA) or of salts of methanesulfonic acid in aqueous metal-working formulations is particularly advantageous.







DETAILED DESCRIPTION

MSA is stable in water and completely soluble in all proportions at ambient temperature. MSA is non-corrosive; in aqueous solution, it liberates no H2S. MSA is readily biodegradable (100% decomposition in 28 days), which is environmentally friendly. MSA confers particularly advantageous extreme pressure properties on the lubricant formulations.


The subject of the present invention is therefore a method for working or forming metals in the presence of an aqueous lubricant containing a water-soluble extreme pressure additive, characterized in that this additive is methanesulfonic acid (MSA) or a water-soluble salt of MSA.


The water-soluble MSA salts according to the invention are obtained by neutralizing MSA with a salifying agent. Salts of alkali or alkaline-earth metals are preferred as water-soluble MSA salts according to the invention, but use can also be made of the water-soluble salts obtained from compounds satisfying the general formula:

R1NR2R3

where the symbols R1, R2 and R3, identical or different, each represent a hydrogen atom, an alkyl, alkenyl or alkylaryl radical with 1 to 22 carbon atoms, or an oxyethylated radical of the form (CH2—CH2—O)nH, where n is between 1 and 20.


Among the alkali metal salts, those obtained by neutralizing MSA with caustic soda or caustic potash are preferred.


As non-limiting examples of R1NR2R3 compounds, mention may be made of alkanolamines, in particular monoethanolamine, diethanolamine or triethanolamine, ethoxylated amines whereof the preferred compounds are those in which R1 is a radical with 12 to 22 carbon atoms, and R2 and R3 are oxyethyl radicals with 1 to 10 ethylene oxide groups.


The salifying agent is added in stoichiometric proportion with respect to the MSA, in excess with respect to the MSA, or in deficiency with respect to the MSA, depending on the pH desired for the final formulation. Preferably, the molar ratio between the MSA and the salifying agent is between 1:1 and 1:2.


The water-soluble MSA salts according to the invention are perfectly stable in water at ambient temperature and can be used to obtain concentrated or dilute aqueous lubricant formulations which are easily stored without liberating any H2S and have particularly advantageous extreme pressure properties.


Furthermore, these formulations are not corrosive.


The MSA or water-soluble MSA salts can be in the form of a concentrate that can subsequently be diluted during use, or in the form of a dilute solution. They can be used alone, but in general they are used in a mixture with other common additives of synthetic or semisynthetic fluids for metal working or forming. These additives include bactericides, emulsifiers, lubricity promoters, antiwear additives, antifoams and corrosion inhibitors.


The concentrates contain between 10% and 50% by weight of MSA or of water-soluble MSA salt, and preferably between 15% and 35%.


The MSA or the water-soluble MSA salts according to the invention, the concentrates containing same, and other additives conventionally found in aqueous lubricants for metal working or forming, can be incorporated with the aqueous lubricants commonly employed for metal working or forming, and particularly with the synthetic fluids (true solutions) or semisynthetic fluids (microemulsions), in concentrations between 0.01% and 20% by weight, and preferably between 0.1% and 10% by weight.


The efficiency of the extreme pressure additives according to the invention is evaluated by tests on a 4-ball machine by the 4-ball extreme pressure test according to ASTM Standard D-2783: this test consists in evaluating the extreme pressure capacity of a fluid from the value of the load above which 4 balls are welded together, preventing the rotation of the uppermost ball on the other 3 remaining in the test fluid, according to the following measurement protocol:

    • 100C6 steel balls 12.7 mm in diameter
    • Speed of rotation of the uppermost ball: 1500 revolutions per minute
    • Test duration: 10 seconds
    • Increasing loads.


The load corresponding to the welding of the 4 balls corresponds to the extreme pressure capacity; it must be as high as possible, typically=160 kg.


The anticorrosion power of the extreme pressure additives according to the invention is evaluated by contacting chips of cast iron with the aqueous lubricant to be tested by the following protocol:

    • 2 g of standard cast iron chips (ASTM D4627) are covered with 5 ml of aqueous lubricant to be tested in a petri dish with a filter paper on the bottom.
    • Contact time: 2 hours at ambient temperature.


The appearance of rust on the filter paper is the indicator of the anticorrosion power; the grading is shown in Table 1:












TABLE 1







Observation on the filter paper
Anticorrosion power









No trace of rust
Good



Few traces of rust
Medium



Traces of rust
Poor











The following examples illustrate the invention without limiting it. The percentages indicated are expressed by weight.


EXAMPLES
Example 1

Table 2 shows the composition and extreme pressure performance of the different formulations tested; these are dilute aqueous formulations of MSA or 1:1 water-soluble MSA salts. They contain 5% by weight of water-soluble additive.


These formulations are obtained at ambient temperature in a 300 ml beaker containing 200 ml of double-distilled water. The adequate quantity of pure MSA is slowly added with moderate magnetic stirring. The caustic soda (NaOH), caustic potash (KOH), monoethanolamine (MEA), triethanolamine (TEA) or ethoxylated fatty amine (NORAMOX® C2: monoamine on ethoxylated copra base with 2 moles of ethylene oxide or NORAMOX® O2: monoamine on ethoxylated oleic base with 2 moles of ethylene oxide, manufactured by CECA) is then added in stoichiometric proportions to obtain a 1:1 salt containing 5% by weight of active material. The solutions are all clear, stable and without any particular odor. Each of the compositions was subjected to the 4-ball test with determination of the welding load.












TABLE 2









Composition
Welding load










Formulation
Water (in %)
Additive (in %)
(in kg)













Control
100
None
80











1
95
MSA
5
400


2
95
MSA
3.53
400




NaOH
1.47


3
95
MSA
3.16
400




KOH
1.84


4
95
MSA
3.06
250




MEA
1.94


5
95
MSA
1.96
200




TEA
3.04


6
95
MSA
1.19
160




Noramox C2
3.81


7
95
MSA
1.04
160




Noramox O2
3.96









An examination of the results of the 4-ball test reveals that the lubricant formulations based on MSA or a water-soluble MSA salt according to the invention help to obtain a welding load=160 kg, much higher than the load measured with pure water used as a control. The incorporation of an additive based on MSA or a water-soluble MSA salt according to the invention helps to provide extreme pressure properties to the aqueous formulations used for metal working or forming. The MSA and Na and K salts of MSA help to obtain the highest efficiency.


Example 2

Table 3 shows the extreme pressure performance and corrosion properties of two aqueous lubricants containing a water-soluble MSA salt according to the invention. These compositions are prepared by neutralizing MSA with an excess of caustic soda (NaOH) or monoethanolamine (MEA). The water-soluble salt is in a concentration of 5% by weight in water; the compositions are clear, stable and without any particular odor.














TABLE 3









Weld-
Anti-


Formul-
AMS
NaOH
MEA
ing load
corro-


ation
(in moles)
(in moles)
(in moles)
(in kg)
sion grade







8
1
1.25

500
Good


9
1

2
200
Good









Compositions 8 and 9 according to the invention help to obtain high welding loads in the 4-ball EP test. They have good corrosion properties.

Claims
  • 1. A method for working or forming metals in the presence of an aqueous lubricant wherein the improvement comprises adding a water-soluble extreme pressure additive comprising from about 0.01 to about 20 percent by weight a water-soluble salt of methanesulfonic acid comprising a salt of an alkali or alkaline-earth metal, or of a compound of the formula: R1NR2R3 wherein R1, R2 and R3, are identical or different, each a hydrogen atom, an alkyl, alkenyl or alkylaryl radical with 1 to 22 carbon atoms, or an oxyethylated radical of the form (CH2-CHrO)nH, where n is between 1 and 20 to said aqueous lubricant.
  • 2. The method as claimed in claim 1, wherein said water soluble methanesulfonic acid salt is a sodium or potassium salt.
  • 3. The method as claimed in claim 1, wherein said compound of the formula R1NR2R3 is an alkanolamine.
  • 4. The method of claim 3 wherein said alkanolamine is a monoethanolamine, diethanolamine or triethanolamine.
  • 5. The method as claimed in claim 1, wherein said compound of the formula R1NR2R3 is an ethoxylated amine in which R1 is a radical with 12 to 22 carbon atoms and R2 and R3 are oxyethylated radicals of the formula (CH2—CH2—O)nH with n between 1 and 10.
  • 6. The method of claimed in claim 1 wherein the concentration of water-soluble methanesulfonic acid salt in said aqueous lubricant is between about 0.1% and 10% by weight.
Priority Claims (1)
Number Date Country Kind
01 14787 Nov 2001 FR national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/FR02/03847 11/8/2002 WO 00 5/13/2004
Publishing Document Publishing Date Country Kind
WO03/042342 5/22/2003 WO A
US Referenced Citations (61)
Number Name Date Kind
2540534 Kolfenbach et. al. Feb 1951 A
2841554 Ambrose et al. Jul 1958 A
3388062 Vaughn Jun 1968 A
3928215 Dreher et al. Dec 1975 A
4036764 Fischer et al. Jul 1977 A
4079012 Bosniack Mar 1978 A
4181624 Koch Jan 1980 A
4212750 Gorman Jul 1980 A
4239634 Marin et al. Dec 1980 A
4379063 Williams Apr 1983 A
4505830 Vinci Mar 1985 A
4560488 Vinci Dec 1985 A
4606833 Schuettenberg et al. Aug 1986 A
4620855 Higgius Nov 1986 A
4659488 Vinci Apr 1987 A
4670172 Sproul et al. Jun 1987 A
4747972 Holden et al. May 1988 A
4759861 Ogura et al. Jul 1988 A
4778614 Rawlinson et al. Oct 1988 A
4828657 Fukuoka et al. May 1989 A
4880552 Guesnet et al. Nov 1989 A
4923887 Bauer et al. May 1990 A
5312974 Wuest et al. May 1994 A
5322631 Fuchigami et al. Jun 1994 A
5352373 Goto Oct 1994 A
5367903 Keller Nov 1994 A
5449470 Cahoon et al. Sep 1995 A
5599780 Koyama et al. Feb 1997 A
5733853 Bardasz et al. Mar 1998 A
5908816 Kobessho et al. Jun 1999 A
6040281 Bereuter et al. Mar 2000 A
6190574 Nakagawa et al. Feb 2001 B1
6204228 MacNeil et al. Mar 2001 B1
6355604 Guillemet Mar 2002 B2
6376433 Connor Apr 2002 B1
6410491 Harrison et al. Jun 2002 B1
6436882 Rizvi Aug 2002 B1
6562766 Koyama et al. May 2003 B1
6602833 Skold Aug 2003 B1
6706670 Kalota et al. Mar 2004 B2
6764982 Bardasz et al. Jul 2004 B2
6787192 Fukumura et al. Sep 2004 B2
6809069 Deshimaru et al. Oct 2004 B2
6828286 Komiya et al. Dec 2004 B2
7008909 Burgo et al. Mar 2006 B2
7018959 McCullough et al. Mar 2006 B2
7285516 Carrick et al. Oct 2007 B2
7332461 Eastwood Feb 2008 B2
20020106978 Michaud et al. Aug 2002 A1
20030130142 Nguyen Jul 2003 A1
20030159938 Hradil Aug 2003 A1
20030220206 Komiya et al. Nov 2003 A1
20040149587 Hradil Aug 2004 A1
20050164610 Michaud et al. Jul 2005 A1
20050288193 Fujimaki et al. Dec 2005 A1
20060111252 Costello et al. May 2006 A1
20060113195 Hradil et al. Jun 2006 A1
20060156774 Inoue Jul 2006 A1
20060183649 Costello et al. Aug 2006 A1
20060223719 Riff et al. Oct 2006 A1
20070004600 Stoneman et al. Jan 2007 A1
Foreign Referenced Citations (7)
Number Date Country
318736 Jun 1989 EP
915183 Nov 2003 EP
60228541 Nov 1985 JP
63-265997 Nov 1988 JP
10-110181 Apr 1998 JP
1335562 Sep 1987 SU
WO 03042342 May 2003 WO
Related Publications (1)
Number Date Country
20050044912 A1 Mar 2005 US