US2944973A - Di-ester fluids with improved water tolerance - Google Patents
Di-ester fluids with improved water tolerance Download PDFInfo
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- US2944973A US2944973A US546790A US54679055A US2944973A US 2944973 A US2944973 A US 2944973A US 546790 A US546790 A US 546790A US 54679055 A US54679055 A US 54679055A US 2944973 A US2944973 A US 2944973A
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular 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
- C10M2209/084—Acrylate; Methacrylate
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/108—Phenothiazine
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/02—Unspecified siloxanes; Silicones
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/08—Resistance to extreme temperature
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/06—Instruments or other precision apparatus, e.g. damping fluids
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
- C10N2040/13—Aircraft turbines
Definitions
- DI-ESTER FLUIDS WITH rinnovan WATER TOLERANCE Theodore W. Langer, Buffalo, and Blake F. Mago, North Tonawanda, N.Y., assignors to Union Carbide Corporation, a corporation of New York No Drawing. Filed Nov. 14, 1955, Ser. No. 546,790
- This invention generally relates to aliphatic di-ester fluids having improved water tolerance. It is concerned more particularly with mixtures of such di-esters with polyoxyalkylene glycols.
- Di-ester type fluids including substituted adipates, azelates and sebacates, find extensive use as high temperature turbine lubricants for aircraft engines, instruments and in general wherever excellent viscosity-solubility and viscosity-temperature properties are needed. These fluids, however, possess the unwanted tendency of dissolving or absorbing small amounts of Water. This solubility decreases at lower temperatures, and condensate absorbed by the fluids at operating temperatures later precipitates as ice after shut down at winter temperatures. Precipitation of the thus formed ice in oil lines or at nozzles can cause clogging.
- polyoxyalkylene glycol derivatives are the addition products formed by the reaction of an alcohol with ethylene oxide, or propylene oxide or a mixture of these oxides in which the ratios of the respective oxides are from about 25 percent-75 percent to 75 percent-25 percent.
- Such products are viscous liquids of relatively high average molecular weight, and actually are complex mixtures of polyoxyalkylene chains having different lengths.
- the lubricant fluid of the invention thus comprises a mixture of di-alkyl esters of simple and substituted d-i-basic acids having from 6 to 10 carbon atoms, and polyoxy alkylene glycols and mono and di-ether derivatives thereof having a viscosity ranging from 59 to 3000 SUS at 100 F.
- the cloud point is the temperature at which a definite turbidity is noted on cooling the fluid. This was determined by observing the sample in a test tube immersed in a cold bath. A thermometer placed in the sample was read when turbidity was first evident.
- Table I indicates that as di-esters absorb water from the atmosphere, their cloud points are raised objectionably.
- a quantity of di-2-ethylhexyl sebacate as received from a manufacturer contained 0.06 percent water, and di-2-ethylhexyl adipate from another source absorbed 0.09 percent water; Accordingly, both were turbid on standing at about 20 F.
- Table 'II cites examples showing that the water tolerance of di-Z-ethylhexyl adipate was increased appreciably by the addition of various polyoxyalkylene glycol derivatives.
- A is a polyoxypropylene glycol monobutyl ether having a viscosity of 3,000 SUS at F.
- B is a polyoxypropylene glycol dibutyl ether having a viscosity of SUS at 100 F.
- C is a butyl ethyl diether of a polyalkylene glycol made from a 5050 mixture of propylene and ethylene oxide with the final diether having a viscosity of 59 SUS at 100 F.
- organophosphate compounds of the type obtained by the reaction of inorganic phosphorus compounds with petroleum fractions (exampletricresylphosphate).
- inorganic phosphorus compounds with petroleum fractions (exampletricresylphosphate).
- Conventional corrosion problems are resolved through the selection of base fluid blends, together with proper choosing of additives for other purposes, as Well as by the addition of specific corrosion inhibitors.
- Viscosity tailoring of fluid may be eflccted by the addition of selected polymers such as polymethylmethacryl-ate or silo-xanes. Accordingly, various modifications and variations may be effected as regards these conventional additives without departing from therange of the invention or from the scope of the appended claims.
- a lubricant fluid having improved viscometric stability and low temperature Water tolerance consisting of 5 percent polyoxypropylene glycol monobutyl ether, 5 percent tri-cresyl phosphate, 0.5 percent phenothiazine, the balance di-Z-ethylhexyl adipate, said mixture having a Hardiman and Nissan viscosity index of 15-4.
- a lubricant fluid consisting of a mixture of di-2- ethylhexyl adipate plus 22 /2 percent of polyoxyprop y-lene glycol dibutyl other, 5 percent tri-cresyl phosphate and 0.5 percent of phenothiazine, said mixture having a viscosity of about 12,000 centistokes at --6'5 F. and a H-ardiman and Nissan viscosity index of 149.
- a lubricant fluid for gas turbine engines consisting of 6-percent polyoxypropylene glycol monobutyl ether, 5 percent .tri-cresyl phosphate, 10.5 percent phenothiazine, the balance consisting of mixed alcohol pimelates, said mixture having a viscosity of about 7,600 centistokes at -65 F. and a Hardiman and Nissan viscosity index of about 159.
- a lubricant fluid for gas turbine engines consisting of 80 percent di-Z-ethylhexyl adipa te and 20 percent of a polyoxypl'opylene glycol dibutyl ether having a viscosity of 130 Saybolt Universal seconds at 100 F.
- a lubricant fluid for gas turbine engines consisting of 90 percent of di-Z-ethylhexy-l adipate and 10 percent of a butyl ethyl diether of a polyoxya-lkylene glycol of a viscosity of 59 Saybolt Universal seconds at 100 F.
- a lubricant and hydraulic fluid mixture having improved viscometric stability and low temperature water tolerance containing, in addiiion i0 conventional additives for the control of oxidation, lubricity, corrosion and viscosity, 20 percent of polyoxypropylene glycol di-butyl ether having a viscosity of 130 Saybolt Universal seconds at 100 F the balance being di-Z-ethylhexyl adipate.
- a lubricant and hydraulic fluid mixture having improved viscometric stability and low temperature Water tolerance containing in addition to conventional additives for the control of oxidation, lubricity, corrosion and viscosity, 10 percent of a butyl ethyl di-ether of a polyoxyalkylene glycol having a viscosity of 59 Saybolt Universal seconds at 100" F., the balance being di-Z-ethylhexyl adipate.
- a lubricant and hydraulic fluid having improved viscometric stability and low temperature water tolerance consisting essentially of a mixture composed of at least one aliphatic diester selected from the group consisting of the higher alkyl adipates, sebacates, azelates and pimelatcs, and from 2 to 22% percent of at least one high viscosity alkyl polyoxyalkylene glycol other selected from the group consisting of lower alkyl monoand di-ethers of polyoxypropylene and polyoxyethylcne glycols, the vis cosity of said ether ranging from about 59 Saybolt Universal seconds to about 3000 Saybolt Universal seconds at F.
- the fluid of claim 8 additionally characterized by the presence therein of conventional additives for the control of oxidation, lubricity, corrosion and viscosity.
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Description
DI-ESTER FLUIDS WITH rinnovan WATER TOLERANCE Theodore W. Langer, Buffalo, and Blake F. Mago, North Tonawanda, N.Y., assignors to Union Carbide Corporation, a corporation of New York No Drawing. Filed Nov. 14, 1955, Ser. No. 546,790
9 Claims. (Cl. 252-475) This invention generally relates to aliphatic di-ester fluids having improved water tolerance. It is concerned more particularly with mixtures of such di-esters with polyoxyalkylene glycols.
Di-ester type fluids, including substituted adipates, azelates and sebacates, find extensive use as high temperature turbine lubricants for aircraft engines, instruments and in general wherever excellent viscosity-solubility and viscosity-temperature properties are needed. These fluids, however, possess the unwanted tendency of dissolving or absorbing small amounts of Water. This solubility decreases at lower temperatures, and condensate absorbed by the fluids at operating temperatures later precipitates as ice after shut down at winter temperatures. Precipitation of the thus formed ice in oil lines or at nozzles can cause clogging.
It has been found that the water tolerance and viscometric stability of the above di-ester fluids can be increased by the addition of polyoxyalkylene glycol derivatives. These derivatives are the addition products formed by the reaction of an alcohol with ethylene oxide, or propylene oxide or a mixture of these oxides in which the ratios of the respective oxides are from about 25 percent-75 percent to 75 percent-25 percent. Such products are viscous liquids of relatively high average molecular weight, and actually are complex mixtures of polyoxyalkylene chains having different lengths. For a further and more detailed description of the additives of the invention, reference is made to US. Patents 2,425,755 and 2,425,845, issued August 19, 1947, in the names respectively of F. H. Roberts et a1. and W. J. Toussaint et al.
The lubricant fluid of the invention thus comprises a mixture of di-alkyl esters of simple and substituted d-i-basic acids having from 6 to 10 carbon atoms, and polyoxy alkylene glycols and mono and di-ether derivatives thereof having a viscosity ranging from 59 to 3000 SUS at 100 F.
' To illustrate the eifectiveness of the additives of the invention in improving the water tolerance of di-esters, cloud point determinations were made on two of these.
The cloud point is the temperature at which a definite turbidity is noted on cooling the fluid. This was determined by observing the sample in a test tube immersed in a cold bath. A thermometer placed in the sample was read when turbidity was first evident.
Patented July 12, 1960 Table I indicates that as di-esters absorb water from the atmosphere, their cloud points are raised objectionably. A quantity of di-2-ethylhexyl sebacate as received from a manufacturer contained 0.06 percent water, and di-2-ethylhexyl adipate from another source absorbed 0.09 percent water; Accordingly, both were turbid on standing at about 20 F.
Table 'II cites examples showing that the water tolerance of di-Z-ethylhexyl adipate was increased appreciably by the addition of various polyoxyalkylene glycol derivatives.
A is a polyoxypropylene glycol monobutyl ether having a viscosity of 3,000 SUS at F.
B is a polyoxypropylene glycol dibutyl ether having a viscosity of SUS at 100 F. C is a butyl ethyl diether of a polyalkylene glycol made from a 5050 mixture of propylene and ethylene oxide with the final diether having a viscosity of 59 SUS at 100 F.
TABLE H Examples 1 to 8 Cloud Point with Dl-2- Polyalkylene Ethylhexyl Adipate, F. Example 1-8 Glycol Derivative 0.11% Water 0.16% Water -14 +16 -30 +6 32 +6 -52 -30 30 +5 52 30 -70 45 Below -70 Other diesters show similar beneficial effects from ad- Also, addition of 5 percent polyglycol B to di-Z-ethyl- 'hexyl sebacate containing 0.06 percent of water by Karl Fischer analysis lowered the ester cloud point from 20 F. to below the pour point of the fluid. Storage. tests of 72 hours duration at a 65 F. temperature with di-2- ethylhexyl ad-ipate containing 0.09 percent water indicated that 10 percent of polypropylene oxide monobutyl ether of a viscosity of 525 Saybolt Universal seconds (SUS), 6.5 percent of the same type of polyglycol having a viscosity of 1145 Saybolt seconds or 6 percent of the samehav-ing a viscosity of 1715 Saybolt seconds, or 22.5 percent polypropoxy dibutyl ether of a viscosity of 130 Saybolt seconds, result in clear blends. This is to be contrasted with samples of the adipate alone or mixed with polymethylmethacrylate thickeners which become turbid afiter similar exposure.
Another advantage of mixtures of di-esters with poly-' oxyalkylene glycols is the marked improved-temperature TABLE IV Examples 12 to 18 Corrosion-inhibited Blend Con- Viscosity (cstks) Hardi- Exaruple taming Tricresyl Phosphate man and and 0.5% Phenothiazine Nissan 210 F. 100 F. 65 F. V.I.
12 Di-2ethy1hexyl sebacate 3.35 13.3 12,600 143 13 Di-2-ethylhexyl adipate 2. 40 8.45 6,650 130 14 Dl-Z-ethylhexyl adipate plus 5 per- 3. 14 11.27 154 cent of A. 15 Di-2-ethylhexyl adipate plus 22.5 3.01 11.10 12, 400 149 percent of B. 16 Mixed alcohol pimelate 2. 33 7. 94 150 17 Mixed alcohol pimelate plus 6 per- 3. 26 11. 36 7, 650 159 cent of A. 18 Mixed alcohol pimelate plus 25 3.10 11.07 9, 450 154 percent of B. p
The foregoing additives in general gave better performance than unblocked polyglycols such as polypropylene glycol. Such compounds have applicability in particular cases. Typically the performance of polypropylene glycol appears in Table V.
It is to be understood that the benefits obtained by the addition of polyoxyalkylene glycols to aliphatic di-ester fluids are realized in the presence of other agents which may be added to the base fluids to overcome other performance problems. The end use of these fluids, for example, hydraulic fluids for aircraft engines, may require the inclusion of other additives for control of oxidation, lubricity, corrosion and viscosity tailoring. Oxidation control additives generally consist of aromatic amines such as phenothiazine or substituted phenols, and sometimes may contain sulfur. Improved lubricity or load-carrying ability can be secured by the addition of organophosphate compounds of the type obtained by the reaction of inorganic phosphorus compounds with petroleum fractions (exampletricresylphosphate). Conventional corrosion problems are resolved through the selection of base fluid blends, together with proper choosing of additives for other purposes, as Well as by the addition of specific corrosion inhibitors. Viscosity tailoring of fluid may be eflccted by the addition of selected polymers such as polymethylmethacryl-ate or silo-xanes. Accordingly, various modifications and variations may be effected as regards these conventional additives without departing from therange of the invention or from the scope of the appended claims.
What is claimed is:
1. A lubricant fluid having improved viscometric stability and low temperature Water tolerance consisting of 5 percent polyoxypropylene glycol monobutyl ether, 5 percent tri-cresyl phosphate, 0.5 percent phenothiazine, the balance di-Z-ethylhexyl adipate, said mixture having a Hardiman and Nissan viscosity index of 15-4.
2. A lubricant fluid consisting of a mixture of di-2- ethylhexyl adipate plus 22 /2 percent of polyoxyprop y-lene glycol dibutyl other, 5 percent tri-cresyl phosphate and 0.5 percent of phenothiazine, said mixture having a viscosity of about 12,000 centistokes at --6'5 F. and a H-ardiman and Nissan viscosity index of 149.
3. A lubricant fluid for gas turbine engines consisting of 6-percent polyoxypropylene glycol monobutyl ether, 5 percent .tri-cresyl phosphate, 10.5 percent phenothiazine, the balance consisting of mixed alcohol pimelates, said mixture having a viscosity of about 7,600 centistokes at -65 F. and a Hardiman and Nissan viscosity index of about 159.
4. A lubricant fluid for gas turbine engines consisting of 80 percent di-Z-ethylhexyl adipa te and 20 percent of a polyoxypl'opylene glycol dibutyl ether having a viscosity of 130 Saybolt Universal seconds at 100 F.
5. A lubricant fluid for gas turbine engines consisting of 90 percent of di-Z-ethylhexy-l adipate and 10 percent of a butyl ethyl diether of a polyoxya-lkylene glycol of a viscosity of 59 Saybolt Universal seconds at 100 F.
6. A lubricant and hydraulic fluid mixture having improved viscometric stability and low temperature water tolerance containing, in addiiion i0 conventional additives for the control of oxidation, lubricity, corrosion and viscosity, 20 percent of polyoxypropylene glycol di-butyl ether having a viscosity of 130 Saybolt Universal seconds at 100 F the balance being di-Z-ethylhexyl adipate.
7. A lubricant and hydraulic fluid mixture having improved viscometric stability and low temperature Water tolerance containing in addition to conventional additives for the control of oxidation, lubricity, corrosion and viscosity, 10 percent of a butyl ethyl di-ether of a polyoxyalkylene glycol having a viscosity of 59 Saybolt Universal seconds at 100" F., the balance being di-Z-ethylhexyl adipate.
8. A lubricant and hydraulic fluid having improved viscometric stability and low temperature water tolerance, consisting essentially of a mixture composed of at least one aliphatic diester selected from the group consisting of the higher alkyl adipates, sebacates, azelates and pimelatcs, and from 2 to 22% percent of at least one high viscosity alkyl polyoxyalkylene glycol other selected from the group consisting of lower alkyl monoand di-ethers of polyoxypropylene and polyoxyethylcne glycols, the vis cosity of said ether ranging from about 59 Saybolt Universal seconds to about 3000 Saybolt Universal seconds at F.
9. The fluid of claim 8 additionally characterized by the presence therein of conventional additives for the control of oxidation, lubricity, corrosion and viscosity.
References Cited in the file of this patent OTHER REFERENCES Ucon, August 3, 1947, copyright 1947, by Carbide and Carbon Chem. Corp, New York, N.Y., pp. 6-9, 14 and 15.
Claims (1)
- 8. A LUBRICANT AND HYDRAULIC FLUID HAVING IMPROVED VISCOMETRIC STABILITY AND LOW TEMPERATURE WATER TOLERANCE, CONSITING ESSENTIALLY OF A MIXTURE COMPOSED OF AT LEAST ONE ALIPHATIC DIESTER SELECTED FROM THE GROUP CONSISTING OF THE HIGHER ALKYL ADIPATES, SEBACATES, AZELATES AND PIMELATES, AND FROM 2 TO 22 1/2 PERCENT OF AT LEAST ONE HIGH VISCOSITY ALKYL POLYOXYALKYLENE GLYCOL ETHER SELECTED FROM THE GROUP CONSISTING OF LOWER ALKYL MONO- AND DI-ETHERS OF POLYOXYPROPYLENE AND POLYOXYETHYLENE GLYCOLS, THE VISCOSITY OF SAID ETHER RANGING FROM ABOUT 59 SAYBOLT UNIVERSALS SECONDS TO ABOUT 3000 SAYBOLT UNIVERSAL SECONDS AT 100*F.
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US546790A US2944973A (en) | 1955-11-14 | 1955-11-14 | Di-ester fluids with improved water tolerance |
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US546790A US2944973A (en) | 1955-11-14 | 1955-11-14 | Di-ester fluids with improved water tolerance |
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US2944973A true US2944973A (en) | 1960-07-12 |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3164553A (en) * | 1960-12-16 | 1965-01-05 | Union Carbide Corp | Process of treating synthetic lubricating oils with urea |
US3197408A (en) * | 1960-12-16 | 1965-07-27 | Union Carbide Corp | Synthetic functional fluids |
US3247111A (en) * | 1963-04-08 | 1966-04-19 | Socony Mobil Oil Co | High temperature jet lubricant |
US3296135A (en) * | 1963-02-08 | 1967-01-03 | Union Carbide Corp | Lubricant compositions having improved corrosion and oxidation properties |
US3337457A (en) * | 1964-02-11 | 1967-08-22 | Exxon Research Engineering Co | Crankcase lubricants comprising a mineral and synthetic ester oil blend |
US3609085A (en) * | 1970-03-16 | 1971-09-28 | Monsanto Co | Polyester functional fluid compositions |
US3640858A (en) * | 1968-11-14 | 1972-02-08 | Texaco Inc | Dual purpose lubricating compositions |
EP0190869A2 (en) * | 1985-01-31 | 1986-08-13 | Exxon Chemical Patents Inc. | Lubricating oil composition |
EP0227477A2 (en) * | 1985-12-23 | 1987-07-01 | The Dow Chemical Company | Lubricants for reciprocating air compressors |
DE3737782A1 (en) * | 1987-11-06 | 1989-05-18 | Toyota Motor Co Ltd | SYNTHETIC LUBRICANTS |
US5503762A (en) * | 1992-07-08 | 1996-04-02 | Henkel Kommanditgesellschaft Auf Aktien | Base oils with a high viscosity index and improved low-temperature behavior |
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US2390258A (en) * | 1943-05-24 | 1945-12-04 | Hydraulic Brake Co | Hydraulic pressure fluid |
US2402754A (en) * | 1943-05-24 | 1946-06-25 | Hydraulic pressure fluid | |
GB601419A (en) * | 1944-12-13 | 1948-05-05 | Carbide & Carbon Chem Corp | Improvements in or relating to synthetic lubricant compositions |
US2485376A (en) * | 1947-02-13 | 1949-10-18 | Rohm & Haas | Corrosion-resisting lubricating compositions |
US2534803A (en) * | 1946-01-11 | 1950-12-19 | Automotive Prod Co Ltd | Power transmission fluids |
US2599803A (en) * | 1948-11-01 | 1952-06-10 | Shell Dev | Lubricating composition |
US2698837A (en) * | 1950-11-15 | 1955-01-04 | Monsanto Chemicals | Functional fluids |
US2755251A (en) * | 1953-07-17 | 1956-07-17 | Atlas Powder Co | Hydraulic fluid compositions |
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1955
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Publication number | Priority date | Publication date | Assignee | Title |
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US2390258A (en) * | 1943-05-24 | 1945-12-04 | Hydraulic Brake Co | Hydraulic pressure fluid |
US2402754A (en) * | 1943-05-24 | 1946-06-25 | Hydraulic pressure fluid | |
GB601419A (en) * | 1944-12-13 | 1948-05-05 | Carbide & Carbon Chem Corp | Improvements in or relating to synthetic lubricant compositions |
US2534803A (en) * | 1946-01-11 | 1950-12-19 | Automotive Prod Co Ltd | Power transmission fluids |
US2485376A (en) * | 1947-02-13 | 1949-10-18 | Rohm & Haas | Corrosion-resisting lubricating compositions |
US2599803A (en) * | 1948-11-01 | 1952-06-10 | Shell Dev | Lubricating composition |
US2698837A (en) * | 1950-11-15 | 1955-01-04 | Monsanto Chemicals | Functional fluids |
US2755251A (en) * | 1953-07-17 | 1956-07-17 | Atlas Powder Co | Hydraulic fluid compositions |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3164553A (en) * | 1960-12-16 | 1965-01-05 | Union Carbide Corp | Process of treating synthetic lubricating oils with urea |
US3197408A (en) * | 1960-12-16 | 1965-07-27 | Union Carbide Corp | Synthetic functional fluids |
US3296135A (en) * | 1963-02-08 | 1967-01-03 | Union Carbide Corp | Lubricant compositions having improved corrosion and oxidation properties |
US3247111A (en) * | 1963-04-08 | 1966-04-19 | Socony Mobil Oil Co | High temperature jet lubricant |
US3337457A (en) * | 1964-02-11 | 1967-08-22 | Exxon Research Engineering Co | Crankcase lubricants comprising a mineral and synthetic ester oil blend |
US3640858A (en) * | 1968-11-14 | 1972-02-08 | Texaco Inc | Dual purpose lubricating compositions |
US3609085A (en) * | 1970-03-16 | 1971-09-28 | Monsanto Co | Polyester functional fluid compositions |
EP0190869A2 (en) * | 1985-01-31 | 1986-08-13 | Exxon Chemical Patents Inc. | Lubricating oil composition |
EP0190869A3 (en) * | 1985-01-31 | 1987-11-25 | Exxon Chemical Patents Inc. | Lubricating oil composition |
US4891145A (en) * | 1985-01-31 | 1990-01-02 | Exxon Chemical Patents Inc. | Lubricating oil composition |
EP0227477A2 (en) * | 1985-12-23 | 1987-07-01 | The Dow Chemical Company | Lubricants for reciprocating air compressors |
EP0227477A3 (en) * | 1985-12-23 | 1987-11-25 | The Dow Chemical Company | Lubricants for reciprocating air compressors |
DE3737782A1 (en) * | 1987-11-06 | 1989-05-18 | Toyota Motor Co Ltd | SYNTHETIC LUBRICANTS |
US4968453A (en) * | 1987-11-06 | 1990-11-06 | Toyota Jidosha Kabushiki Kaisha | Synthetic lubricating oil composition |
US5503762A (en) * | 1992-07-08 | 1996-04-02 | Henkel Kommanditgesellschaft Auf Aktien | Base oils with a high viscosity index and improved low-temperature behavior |
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