Perfluorinated polyether lubricant compositions
A lubricant composition comprises a perfluorinated polyalkylether base fluid (PFPAE) and an oxidation-corrosion inhibiting amount of a perfluoro-substituted benzothiazole or bis-benzothiazole. The benzothiazole compound additive exhibits excellent solubility in the base fluid and possesses outstanding low volatility characteristics. As a result, the lubricant composition functions as a noncorrosive, stable material suitable for long term applications over a wide temperature range (-65.degree. F. to >600.degree. F.) in an oxidative environment.The perfluoro-substituted benzothiazoles and bis-benzothiazoles have the formula: Q--R.sub.f or Q--R.sub.f '--Q, wherein Q is ##STR1## wherein R.sub.f is a linear or branched perfluoroalkylether group containing at least one ether linkage and R.sub.f ' is a linear or branched perfluoroalkyleneeher group containing at least one ether linkage.In formulating the lubricant composition of this invention, an oxidation-corrosion inhibiting amount of the substituted benzothiazole is dissolved in the PFPAE base fluid. The amount of the benzothiazole employed generally ranges from about 0.05 to 5.0 weight percent, preferably about 0.5 to 2.0 weight percent, based on the weight of the base fluid. This provides a lubricant containing an amount of oxidation-corrosion inhibiting additive that is adequate for long term applications at elevated temperatures while maintaining excellent formulation stability after storage at low temperatures for long periods of time.
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This invention relates to oxidation-corrosion inhibitors for perfluoropolyalkylether fluids.
Highly fluorinated compounds have long been of interest because of their excellent potential for high temperature applications. Fluids based on perfluoropolyalkylethers (PFPAE) have, in addition to high thermal and oxidative stability, a wide liquid range which make them ideal candidates for aerospace applications. These fluids consist essentially of a mixture of fluorinated polyethers. These fluids have the general formulae:
R.sub.f O(Z).sub.m R.sub.f
wherein R.sub.f is a lower perfluoroalkyl group, such as CF.sub.3, C.sub.2 F.sub.5, C.sub.3 F.sub.7 and the like, wherein Z is --CX.sub.2 CX.sub.2 O--, --CX.sub.2 CX.sub.2 CX.sub.2 O--or --CX.sub.2 OCX.sub.2 CX.sub.2 O--, where X is --F, --CF.sub.3, --C.sub.2 F.sub.5 and the like, and m has a value of 5 to 50; or
R.sub.f O(Z).sub.n (Y).sub.p R.sub.f
wherein Y is --CFXO--, wherein X, R.sub.f and Z are as previously defined, and n and p are integers whose sum is between 5 and 200 and the ratio of p to n is between 0.1 and 10, and wherein the Z and Y units are statistically distributed along the PFPAE chain. Commercial base fluids have been available for some time, for example, Krytox.sup.R (DuPont), Fomblin.sup.R (Ausimont), Demnum.sup.R (Daikin) and the like. Their practical utility in aerospace and military applications has been hampered by the wear and corrosion of certain metal components exposed to these base fluids under extreme conditions.
Deficiencies in base fluids are generally removed and the performance of the fluids improved by the use of additives. Conventional additives developed for the improvement of a variety of specific properties of hydrocarbon base fluids are generally not suitable for perfluorinated fluids. These conventional additives are not soluble in perfluorinated fluids and are ineffective. One way of overcoming this incompatibility is to synthesize compounds containing fluoroalkylether groups plus selected functional groups for specific activity. Although this approach may make the compound soluble in a fluorinated base fluid, mere replacement of hydrocarbon groups with fluorocarbon groups can change the useful properties of the additive itself by changing the properties of the critical functional group present in the additive. These difficulties are well known to those familiar with the art. In spite of these difficulties, a few useful additives have been developed for perfluorinated fluids. One such example is the development of PFAE substituted triphenylphosphines, C. E. Snyder, Jr. and C. Tamborski, U.S. Pat. No. 4,097,388. These additives, when dissolved in PFPAE fluids, have significantly reduced the corrosion of certain metal components exposed to the fluid at high temperatures in an oxidative environment.
Jones et al, U.S. Pat. No. 3,666,769, issued May 30, 1972, disclose certain substituted benzothiazoles having in their 2-position a perfluoroalkyl, pefluoroaryl, perfluoro(alkoxyalkyl), perfluoro(aryloxyalkyl) or a polyoxyperfluoroalkylene substituent free of either olefinic or acetylenic unsaturation. These substituted benzothiazoles are very stable to high temperatures and are useful as turbine fluids, hydraulic fluids, lubricants, solvents and heat-transfer fluids.
We have discovered that these substituted benzothiazoles can be employed in small quantities to enhance the stability of fluorinated base fluids.
Accordingly, it is an object of this invention to provide perfluorinated fluids having improved stability properties.
Another object of this invention is to provide novel stability enhancing additives for perfluoropolyalkylethers.
Other objects and advantages of the invention will be apparent to those skilled in the art.
SUMMARY OF THE INVENTIONThe present invention resides in a lubricant composition comprising a perfluorinated polyalkylether base fluid and an oxidation-corrosion inhibiting amount of a perfluoro-substituted benzothiazole. The benzothiazole compound additive exhibits excellent solubility in the base fluid and possesses outstanding low volatility characteristics. As a result, the lubricant composition functions as a noncorrosive, stable material suitable for long term applications over a wide temperature range (-65.degree. F. to >600.degree. F.) in an oxidative environment.
The perfluoro-substituted benzothiazoles used as corrosion inhibitors in the lubricant composition of this invention have the following formula:
Q--R.sub.f or Q--R.sub.f '--Q
wherein Q is ##STR2## wherein R.sub.f is a linear or branched perfluoroalkylether group containing at least one ether linkage and R.sub.f ' is a linear or branched perfluoroalkyleneether group containing at least one ether linkage. R.sub.f and R.sub.f ' preferably contain at least two ether linkages.
Examples of the perfluoroalkyleher and perfluoroalkyleneether groups include the following wherein R.sub.f can be ##STR3## wherein x has a value of 1 to 20, preferably 3 to 8; and wherein R.sub.f ' can be ##STR4## wherein x is as defined above, and y and z each has a value of 1 to 20, preferably 1 to 5.
In formulating the lubricant composition of this invention, an oxidation-corrosion inhibiting amount of the substituted benzothiazole is dissolved in the PFPAE base fluid. The amount of the benzothiazole employed generally ranges from about 0.05 to 5.0 weight percent, preferably about 0.5 to 2.0 weight percent, based on the weight of the base fluid. This provides a lubricant containing an amount of oxidation-corrosion inhibiting additive that is adequate for long term applications at elevated temperatures while maintaining excellent formulation stability after storage at low temperatures for long periods of time.
The benzothiazole-substituted perfluoroalkylethers and perfluoroalkyleneethers are prepared by procedures known in the art. One convenient synthesis is given by Jones et al, U.S. Pat. No. 3,666,769, as shown by the following reaction sequence: ##STR5## The perfluoroalkyleneether bis-benzothiazole can be prepared in similar manner.
The following examples illustrate the invention:
EXAMPLE I Synthesis of Q--R.sub.f '--Q, wherein R.sub.f ' is ##STR6## wherein y+z is 3.To a solution of 11.7 g (93.2 mmol) of 2-aminobenzenethiol in 75 ml of anhydrous dietheyl ether was added 25.0 g (23.3 mmol) of the diacid fluoride ##STR7## wherein y+z is 3, over a period of 30 minutes. A mild exotherm was observed during the addition. The reaction mixture was refluxed for 3 hours with stirring. Stirring was then continued at room temperature for an additional 20 hours. At the end of this period, the amine salts had separated as a white solid. This solid was filtered off and the filtrate was treated with 2N HCl (3.times.100 ml) and phase separated. The ether layer was washed with water (2.times.100 ml), phase separated, dried over anhydrous magnesium sulfate and the solvent removed. 28 g of crude product was obtained as a yellow liquid.
The crude product (28 g) was heated with 15 g of polyphosphoric acid (PPA) at 200-250.degree. C. for 2 hours, while stirring the mixture vigorously. Distillation of the reaction mixture yielded 23 g of the bisbenzothiazole (yield, 79%; b.p. 197.degree. C./0.03 mm Hg). The infrared spectrum of the product did not show any absorption due to NH or C.dbd.O groups and was consistent with the expected structure.
EXAMPLE IIA lubricant composition was formulated using a base fluid of the formula
F(CF.sub.2 CF.sub.2 O).sub.r (CF.sub.2 O).sub.q R.sub.f
wherein R.sub.f is a perfluoroalkyl group of unspecified length, but probably having 1 or 2 carbon atoms, and q and r are integers such that the fluid has a kinematic viscosity of 17.56 cSt. at 100.degree. F. This base fluid was Fomblin Z, manufactured by Monticatini Edison of Milan, Italy, and was from the Brayco line of perfluoroalkylether fluids. One weight percent of a benzothiazole-substituted perfluoroalkylether of the formula: ##STR8## synthesized following the procedure given in Jones et al, above, was mixed into the base fluid.
A series of ferrous alloy coupons were immersed in the the inhibited fluid composition prepared above. For comparison, tests were also carried out in which specimens were immersed in base fluid which did not contain the oxidation-corrosion inhibiting additive. Air was bubbled through the Fomblin Z, both inhibited and not inhibited, at the rate of one liter per hour for 24 hours. Tests were conducted at constant temperatures of 525.degree. F., 550.degree. F. and 575.degree. F. The alloy specimens as well as the test apparatus were weighed before and after each test. The data obtained are set forth in Table I, below.
TABLE I
______________________________________
BASE
FLUID FORMULATED FLUID
PROPERTIES 525.degree. F.
525.degree. F.
550.degree. F.
575.degree. F.
______________________________________
Kinematic Viscosity
-72.8 +0.50 +0.20 +0.86
Change at 100.degree. F. (%)
Acid Number Change
36.2 <0.05 <0.05 <0.05
(mg KOH/g)
Fluid Loss (wt. %)
48.7 0.00 0.00 0.00
Metal Weight Change
(mg/cm.sup.2)
4140 Steel +0.07 -0.01 +0.13 +0.53
52100 Bearing Steel
+0.13 +0.06 +0.04 +0.02
410 Stainless Steel
-0.19 +0.05 +0.04 0.00
M-50 Tool Steel
+0.08 +0.08 +0.04 +0.65
440C Stainless Steel
+0.14 0.00 -0.05 -0.03
Fluid Appearance
Clear Clear Clear Clear
yellow yellow
______________________________________
EXAMPLE III
A lubricant composition was formulated using a base fluid of the formula ##STR9## wherein R.sub.f is a perfluoroalkyl group of unspecified length, but probably having 2 carbon atoms, and s is an integer such that the fluid has a kinematic viscosity of 282 cSt. at 100.degree. F. This base fluid was Krytox 143 AC fluid, a produce of E I dupont de Nemours Co., Wilmington, Del. One weight percent of a benzothiazole-substituted perfluoroalkylether of the formula: ##STR10## was mixed into the base fluid.
A series of ferrous alloy coupons were immersed in the the inhibited fluid composition prepared above. For comparison, tests were also carried out in which specimens were immersed in base fluid which did not contain the oxidation-corrosion inhibiting additive. Air was bubbled through the Krytox 143 AC, both inhibited and not inhibited, at the rate of one liter per hour for 24 hours. Tests were conducted at constant temperatures of 600.degree. F. and 625.degree. F. The alloy specimens as well as the test apparatus were weighed before and after each test. The data obtained are set forth in Table II, below.
TABLE II
______________________________________
FORMULATED
BASE FLUID FLUID
PROPERTIES 600.degree. F.
625.degree. F.
600.degree. F.
625.degree. F.
______________________________________
Kinematic Viscosity
+0.27 -4.71 +2.90 +3.90
Change at 100.degree. F. (%)
Acid Number Change
0.05 0.10 0.02 0.02
(mg KOH/g)
Fluid Loss (wt. %)
10.62 22.60 0.00 0.10
Metal Weight Change
(mg/cm.sup.2)
4140 Steel -0.80 -5.42 +0.48 +0.38
52100 Bearing Steel
+0.81 -10.52 +0.08 +0.24
410 Stainless Steel
-5.27 -7.73 0.00 +0.03
M-50 Tool Steel
-1.14 -7.78 +0.04 +0.67
440C Stainless Steel
-5.23 -10.76 +0.02 +0.11
Fluid Appearance
Clear Clear Clear Clear
with with straw yellow
ppt. ppt. color color with
fine ppt.
______________________________________
EXAMPLE IV
A lubricant composition was formulated using the Fomblin Z base fluid referred to in Example II. One weight percent of the bis-benzothiazole prepared in Example I was mixed into the base fluid.
A series of ferrous alloy coupons were immersed in the the inhibited fluid composition prepared above. Air was bubbled through the inhibited fluid at the rate of one liter per hour for 24 hours. Tests were conducted at constant temperatures of 550.degree. F. and 575.degree. F. The alloy specimens as well as the test apparatus were weighed before and after each test. The data obtained are set forth in Table III, below, along with data from Example II, Table I, for the base fluid which did not contain the oxidation-corrosion inhibiting additive.
TABLE III
______________________________________
FORMULATED
BASE FLUID
FLUID
PROPERTIES 525.degree. F.
550.degree. F.
575.degree. F.
______________________________________
Kinematic Viscosity
-72.8 +0.40 +1.15
Change at 100.degree. F. (%)
Acid Number Change
36.2 <0.00 0.00
(mg KOH/g)
Fluid Loss (wt. %)
48.7 0.00 0.00
Metal Weight Change
(mg/cm.sup.2)
4140 Steel +0.07 0.00 +0.24
52100 Bearing Steel
+0.13 0.00 -0.27
410 Stainless Steel
-0.19 0.00 0.00
M-50 Tool Steel
+0.08 +0.09 -0.12
440C Stainless Steel
+0.14 -0.04 0.00
Fluid Appearance
Clear Clear Clear
yellow yellow
______________________________________
The data in Tables I-III clearly demonstrate that the lubricant compositions of this invention have little, if any corrosive effect on ferrous alloys. Further, there was insignificant degradation of the base fluids themselves at the elevated temperatures of the tests.
Various modifications may be made to the invention as described without departing from the spirit of the invention or the scope of the appended claims.
Claims
1. A lubricant composition comprising a perfluorinated polyalkylether base fluid and an oxidation-corrosion inhibiting amount of a perfluoro-substituted benzothiazole.
2. The composition of claim 1 wherein said perfluoro-substituted benzothiazole has the formula Q--R.sub.f, wherein Q is ##STR11## and wherein R.sub.f is a linear or branched perfluoroalkylether group containing at least one ether linkage.
3. The composition of claim 1 wherein the amount of said substituted benzothiazole is about 0.05 to 5.0 weight percent.
4. The composition of claim 1 wherein the amount of said substituted benzothiazole is about 0.5 to 2.0 weight percent.
5. The composition of claim 2 wherein R.sub.f is ##STR12## wherein x has a value of 1 to 20.
6. The composition of claim 2 wherein R.sub.f is
7. The composition of claim 5 wherein said base fluid has the general formula F(CF.sub.2 CF.sub.2 O).sub.r (CF.sub.2 O).sub.q R.sub.f, wherein R.sub.f is a perfluoroalkyl group having 1 or 2 carbon atoms, and q and r are integers such that the fluid has a kinematic viscosity of 17.56 cSt. at 100.degree. F. and wherein said x has a value of 3.
8. The composition of claim 5 wherein said base fluid has the general formula ##STR13## wherein R.sub.f is a perfluoroalkyl group having 1 or 2 carbon atoms, and s is an integer such that the fluid has a kinematic viscosity of 282 cSt. at 100.degree. F. and wherein said x has a value of 3.
9. A lubricant composition comprising a perfluorinated polyalkylether base fluid and an oxidation-corrosion inhibiting amount of a perfluoro-substituted bis-benzothiazole.
10. The composition of claim 9 wherein said perfluoro-substituted bis-benzothiazole has the formula Q--R.sub.f '--Q, wherein Q is ##STR14## and wherein R.sub.f ' is a linear or branched perfluoroalkyleneether group containing at least one ether linkage.
11. The composition of claim 9 wherein the amount of said substituted bis-benzothiazole is about 0.05 to 5.0 weight percent.
12. The composition of claim 9 wherein the amount of said substituted bis-benzothiazole is about 0.5 to 2.0 weight percent.
13. The composition of claim 10 wherein R.sub.f ' is ##STR15## wherein y+z is 3.
14. The composition of claim 9 wherein said base fluid has the general formula F(CF.sub.2 CF.sub.2 O).sub.r (CF.sub.2 O).sub.q R.sub.f, wherein R.sub.f is a perfluoroalkyl group having 1 or 2 carbon atoms, and q and r are integers such that the fluid has a kinematic viscosity of 17.56 cSt. at 100.degree. F. and wherein R.sub.f ' is ##STR16## wherein y+z is 3.
| 3666769 | May 1972 | Jones et al. |
| 3715378 | February 1973 | Sianesi et al. |
| 4011267 | March 8, 1977 | Tamborski et al. |
| 4043926 | August 23, 1977 | Snyder et al. |
| 4097388 | June 27, 1978 | Snyder et al. |
| 4120863 | October 17, 1978 | Tamborski et al. |
| 4267348 | May 12, 1981 | Tamborski et al. |
| 4454349 | June 12, 1984 | Tamborski et al. |
| 4681693 | July 21, 1987 | Gavezotti et al. |
| 5124058 | June 23, 1992 | Corti et al. |
| 5169548 | December 8, 1992 | Strepparola et al. |
| 5302760 | April 12, 1994 | Gschwender et al. |
- Christian, John B. "Benzoxazole and benzothiazole anti-rust greases," Lubr. Eng., 36(11), pp. 639-642.
Type: Grant
Filed: Dec 1, 1994
Date of Patent: Jun 4, 1996
Assignee: The United States of America as represented by the Secretary of the Air Force (Washington, DC)
Inventors: Kalathil C. Eapen (Beavercreek, OH), Loomis S. Chen (Fairborn, OH)
Primary Examiner: Charles T. Jordan
Assistant Examiner: Meena Chelliah
Attorneys: Charles E. Bricker, Thomas L. Kundert
Application Number: 8/348,000
International Classification: C10M13528;
