The present invention relates to a fluid containing a sulfur-containing polyalkylene glycol base oil and an antioxidant.
Industrial fluids that are fire resistant, and particularly those that have thermo-oxidative stability, are desirable for high temperature applications such as lubricants and hydraulic fluids in steel processing and power generation. It is a continuous desire and challenge to increase the fire resistance and thermo-oxidative stability of such industrial fluids. Hydrocarbon oils, which are historically used as lubricants, are generally undesirable in such applications because of their combustible nature. Water-based lubricants offer better fire resistant properties than hydrocarbon oils but tend to be unsuitable for use in high temperature applications where water can evaporate. Anhydrous lubricants are typically needed for high temperature applications.
Conventional polyalkylene glycols (PAGs) are known as lubricant base oil alternatives to hydrocarbons and water. Conventional PAGs are PAGs that are initiated using a monol, diol or triol and reacted with ethylene oxide and/or propylene oxide to form polymers which typically have molecular weights greater than 500 g/mol and up to 50,000 g/mol. Lubricant compositions using such conventional PAGs as base oils offer favorable performance benefits as hydraulic fluids and turbine oils. Yet, conventional PAGs tend to suffer from oxidative instability unless an antioxidant is present. Therefore, as antioxidant depletes from a conventional PAG based lubricant composition the oxidative stability of the lubricant suffers undesirably.
It is desirable to identify an industrial fluid that offers fire resistant properties and thermo-oxidative stability while also offering lubricating capabilities of a PAG, especially if the performance of the lubricant base oil exceeds that of conventional PAGs so the oxidative stability of the fluid is less dependent on the amount of antioxidant present.
The present invention offers a fluid with surprisingly high fire resistant properties and thermo-oxidative stability while also offering lubricating capabilities of a PAG. The base oil of the inventive lubricant tends to have higher fire resistance properties and/or thermo-oxidative stability than conventional PAGs.
In a first aspect, the present invention is a fluid comprising a base oil and an antioxidant, the base oil consisting of a sulfur-containing polyalkylene glycol where greater than 80 weight-percent of the fluid is a sulfur-containing polyalkylene glycol and less than one weight-percent of the fluid is water, with weight percent based on total fluid weight and wherein the sulfur-containing polyalkylene glycol is free of oxygen bound directly to sulfur.
In a second aspect, the present invention is a method for using the fluid of the first aspect, the method comprising introducing the fluid of any previous claim into an apparatus as a material selected from a group consisting of hydraulic fluid and lubricating fluid.
The fluid of the present invention is useful as lubricants and hydraulic fluids, especially for use in high temperature and high pressure applications where aqueous lubricants are undesirable.
“And/or” means “and, or alternatively”. All ranges include endpoints unless otherwise stated.
Test methods refer to the most recent test method as of the priority date of this document unless a date is indicated with the test method number as a hyphenated two digit number. References to test methods contain both a reference to the testing society and the test method number. Test method organizations are referenced by one of the following abbreviations: ASTM refers to ASTM International (formerly known as American Society for Testing and Materials); EN refers to European Norm; DIN refers to Deutsches Institut für Normung; and ISO refers to International Organization for Standards.
Determine kinematic viscosity according to ASTM D7042. Calculate viscosity index for a lubricant formulation according to ASTM D2270. Determine pour point according to ASTM D97. Measure hydroxyl number according to ASTM D4274. Determine fire point values according to ASTM method D92.
The present invention is a fluid comprising a base oil and an antioxidant. The fluid is desirable as a hydraulic fluid and/or lubricant fluid. The fluid is particularly desirable due to its flame retardancy.
The base oil of the present invention is a sulfur-containing polyalkylene glycol (S-PAG) that is free of oxygen bound directly to sulfur. Desirably, the S-PAG comprises copolymerized propylene oxide, butylene oxide or a combination of both copolymerized propylene oxide and butylene oxide. Additionally, or alternatively, the S-PAG can be free of more than two, preferably free of more than one and can be completely free of copolymerized ethylene oxide. Desirably, the S-PAG is free of —C2H4O— components resulting from polymerization of ethylene oxide. For example, —C2H4O— originating from an alcohol initiator (for example, butanol or thiodiglycol) does not contribute a —C2H4O— component resulting from polymerization of ethylene oxide to the resulting S-PAG. For instance, the S-PAG can be free of —C2H4O— groups that are not bound directly to sulfur.
The S-PAG can have the structure of Structure (I):
where R1, R2, R3 and R4 are independently selected from a group consisting of methyl (—CH3) and ethyl (—CH2CH3) groups; R5 is selected from a group consisting of hydrogen, aliphatic groups containing from one to six carbons and aromatic groups containing six carbons; x is a number selected from a group consisting of 1 and 2; m, m′, n, and n′ are independently selected from a number in a range of zero to twenty such that the sum of m, m′, n and n′ is at least six and A is selected from a group consisting of —C2H4— and C6H4 groups. One particularly desirably S-PAG has the structure of Structure (I) where x is one and A is —C2H4—. In addition or as an alternative to any combination of these options for Structure (I), R1, R2, R3 and R4 can all be —CH3 groups. When m, n, m′ and n′ are each one or more then the polymer is a random or block copolymer. A random copolymer occurs when the reactive oxides are simultaneously added to the initiator. As the polymer grows the oxides randomly add to the polymer backbone creating a final random copolymer. A block structure occurs when one oxide is added to the initiator and when this has fully reacted then a second oxide is added. The final structure is described as a block structure since it contains blocks of oxides therein.
The fluid contains greater than 80 weight-percent (wt %), preferably 85 wt % or more, more preferably 90 wt % or more, and can be 95 wt % or more of the S-PAG base oil, with wt % relative to total fluid weight.
The antioxidant of the present invention can be selected from a group consisting of free radical scavengers, peroxide decomposers and phenolic antioxidants. Examples of free radical scavengers include aromatic based aminic antioxidants such as alkylated diphenylamines and phenyl-alpha-naphthylamine and alkylated phenyl-alpha-naphthylamines Peroxide decomposer antioxidants include carbamate type anti-oxidants such as alkylated dithiocarbamates. Free radical scavengers are desirable as antioxidants, especially aminic types. One particularly desirable antioxidant is octylated/butylated diphenylamine
The antioxidant is desirably present at a concentration of 0.25 wt % or more, preferably 0.5 wt % or more and at the same time five wt % or less, preferably two wt % or less with wt % based on total fluid weight.
Less than one wt % of the fluid is water, with wt %. Preferably the fluid contains 0.5 wt % or less, more preferably 0.1 wt % or less, more preferably 0.05 wt % or less and can contain 0.01 wt % or less or even be free of water. Wt% water is relative to total fluid weight. Water is undesirable if the fluid is used in high temperature applications where water may evaporate out from the fluid.
The fluid can contain or be free of any one or any combination of more than one additive including those selected from a group consisting of antiwear, extreme pressure, corrosion inhibitors, yellow metal passivators, dyes and foam control additives.
Surprisingly, it has been discovered with this invention that inclusion of sulfur in the backbone of a PAG can elevate the fire point of the PAG as determined according to ASTM method D92. It has also been surprisingly discovered with this invention that mixing the S-PAG with an antioxidant results in unexpectedly high thermo-oxidative stability relative to similar compositions without having sulfur in the backbone. The enhanced oxidative stability provides longer lifetime for the fluid without suffering from degradation due to oxidation.
A method for using the fluid of the present invention includes introducing the fluid into an apparatus as a material selected from a group consisting of hydraulic fluid and lubricating fluid.
Table 1 identifies materials used in the Examples and Comparative Examples.
Synthesis of S-PAG]: Propylene Oxide Homopolymer of 2,2′-thiodiethanol
Load 1190 grams (g) of 2,2′-thiodiethanol into a stainless steel alkoxylation reactor equipped with a stirrer, an alkylene oxide dosing system, a temperature control system and a means to apply vacuum. Add 26.5 g of a 45 wt % aqueous potassium hydroxide solution as a catalyst. Close the reactor and replace air in the reactor with nitrogen. Heat the reactor to 115 degrees Celsius (° C.) and remove water by applying vacuum at 30 millibar for 120 minutes to reduce the concentration of water to less than 3000 weight-parts per million by weight of total contents weight (ppm). Further heat the reactor to 130° C. and add 4750 g propylene oxide over 6 hours. Once all propylene oxide has been added, stop the propylene oxide feed and maintain the reactor at 130° C. for six hours to allow remaining oxide to react. Treat the resulting polyglycol with magnesium silicate and filter to remove catalyst. The product (S-PAG1) has a kinematic viscosity at 40° C. of 45.8 centistokes (cSt), at 100° C. of 6.96 cSt, a viscosity index of 109 and a hydroxyl number of 188.0 milligrams potassium hydroxide per gram.
S-PAG1 has a structure of that of Structure (I) where R1, R2, R3 and R4 are each methyl, R5 is hydrogen and, on average, the sum of m, m′, n and n′ is 8.4.
Synthesis of S-PAG2: Butylene Oxide Homopolymer of 2,2′-thiodiethanol
Load 582 g of 2,2′-thiodiethanol into a stainless steel alkoxylation reactor equipped with a stirrer, an alkylene oxide dosing system, a temperature control system and a means to apply vacuum. Add 13.9 g of a 45 wt % aqueous potassium hydroxide solution as a catalyst. Close the reactor and replace air in the reactor with nitrogen. Heat the reactor to 115° C. and remove water by applying vacuum at 30 millibar for 120 minutes to reduce the concentration of water to less than 3000 ppm. Further heat the reactor to 130° C. and add 2514 g 1,2-butylene oxide over 6 hours. Once all 1,2-butylene oxide has been added, stop the 1,2-butylene oxide feed and maintain the reactor at 130° C. for six hours to allow remaining oxide to react. Treat the resulting polyglycol with magnesium silicate and filter to remove catalyst. The product (S-PAG2) has a kinematic viscosity at 40° C. of 50.7 cSt, at 100° C. of 6.80 cSt, a viscosity index of 84 and a hydroxyl number of 179.0 milligrams potassium hydroxide per gram.
S-PAG2 has a structure of that of Structure (I) where R1, R2, R3 and R4 are each ethyl, R5 is hydrogen and on average, the sum of m, m′, n and n′ is 7.3.
Synthesis of S-PAG3: Propylene Oxide/Butylene Oxide Random Copolymer of 2,2′-thiodiethanol
Load 600 g of 2,2′-thiodiethanol into a stainless steel alkoxylation reactor equipped with a stirrer, an alkylene oxide dosing system, a temperature control system and a means to apply vacuum. Add 14.2 g of a 45 wt % aqueous potassium hydroxide solution as a catalyst.
Close the reactor and replace air in the reactor with nitrogen. Heat the reactor to 115° C. and remove water by applying vacuum at 30 millibar for 120 minutes to reduce the concentration of water to less than 3000 ppm. Further heat the reactor to 130° C. and add 2590 g of a 50/50 mixture (by weight 0 of propylene oxide and 1,2 butylene oxide over 6 hours. Once all alkylene oxide has been added, stop the alkylene oxide feed and maintain the reactor at 130° C. for six hours to allow remaining oxide to react. Treat the resulting polyglycol with magnesium silicate and filter to remove catalyst. The product (S-PAG3) has a kinematic viscosity at 40° C. of 48.7 cSt, at 100° C. of 7.05 cSt, a viscosity index of 101 and a hydroxyl number of 179.0 milligrams potassium hydroxide per gram.
S-PAG3 has a structure of that of Structure (I) where R1 and R2 are methyl, R3 and R4 are ethyl, on average m+m' is 4.5, n+n' is 3.7.
Characterize the fire point, according to ASTM method D92, of the base oils identified in Table 2. These values serve as reference values for fluid formulations.
Prepare fluids consisting of a base oil and antioxidant as described in Table 3. Wt% is based on total fluid weight. Characterize the fire point for the resulting fluids according to ASTM method D92. Results are in Table 3.
The data in Table 3 reveals that addition of antioxidant tends to increase the fire point of a base oil. However, compared with the data in Table 1, it is evident that S-PAG fluids depend less on the antioxidant to achieve fire point above 275° C. than PAG base oils that do not include sulfur. Therefore, the Examples of the present invention will sustain a higher fire point over the lifetime of the fluid even as antioxidant is consumed.
Characterize the oxidative stability of the fluids identified in Table 4 using a modified ASTM D-2893B test. Place 300 milliliters of the base oil in a borosilicate glass tube and heat to 121° C. under a dry air flow (10 liters per hour flow rate) for 28 days using the equipment described in ASTM D2893. Measure the total acid number (TAN) according to ASTM D664 both initially before heating and after 28 days at the 121° C. The change in TAN value between these two measurements determines whether a fluid passes or fails the oxidative stability test. A small change in TAN value corresponds to higher oxidative stability than a large change in TAN value. Fluids that demonstrate a TAN increase of less than 2.0 mgKOH/g “PASS” and those demonstrating a TAN increase of more than 2.0 mgKOH/g “FAIL” the test.
The data in Table 4 reveals a synergistically enhanced oxidative stability of the S-PAG material in combination with antioxidant. At a 0.5 wt % loading of antioxidant, the fluids with S-PAG base oil easily pass the oxidative stability test while the other base oils unquestionably fail the oxidative stability test even with twice as much antioxidant.
Filing Document | Filing Date | Country | Kind |
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PCT/US2016/047273 | 8/17/2016 | WO | 00 |
Number | Date | Country | |
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62207397 | Aug 2015 | US |