US20030004071A1 - Biodegradable synthetic lubricants - Google Patents
Biodegradable synthetic lubricants Download PDFInfo
- Publication number
- US20030004071A1 US20030004071A1 US10/146,124 US14612402A US2003004071A1 US 20030004071 A1 US20030004071 A1 US 20030004071A1 US 14612402 A US14612402 A US 14612402A US 2003004071 A1 US2003004071 A1 US 2003004071A1
- Authority
- US
- United States
- Prior art keywords
- acids
- ester
- fatty acids
- derived
- sorbitol
- 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.)
- Abandoned
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- 239000000314 lubricant Substances 0.000 title claims description 16
- 150000002148 esters Chemical class 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 22
- 229930195729 fatty acid Natural products 0.000 claims description 22
- 239000000194 fatty acid Substances 0.000 claims description 22
- 150000004665 fatty acids Chemical class 0.000 claims description 21
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 19
- 239000000600 sorbitol Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 17
- 239000012530 fluid Substances 0.000 claims description 14
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical class CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims description 11
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 11
- 238000009472 formulation Methods 0.000 claims description 7
- 229930014626 natural product Natural products 0.000 claims description 7
- 238000005065 mining Methods 0.000 claims description 4
- 239000003240 coconut oil Substances 0.000 claims description 3
- 235000019864 coconut oil Nutrition 0.000 claims description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 2
- 235000005822 corn Nutrition 0.000 claims description 2
- 230000006872 improvement Effects 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 240000008042 Zea mays Species 0.000 claims 1
- 229940049964 oleate Drugs 0.000 description 14
- 150000007513 acids Chemical class 0.000 description 13
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 12
- -1 C12 fatty acids Chemical class 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 238000012065 two one-sided test Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 3
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 239000010720 hydraulic oil Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 229960002446 octanoic acid Drugs 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-M decanoate Chemical compound CCCCCCCCCC([O-])=O GHVNFZFCNZKVNT-UHFFFAOYSA-M 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 231100000584 environmental toxicity Toxicity 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- BTGGRPUPMPLZNT-PGEUSFDPSA-N 2,2-bis[[(z)-octadec-9-enoyl]oxymethyl]butyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(CC)(COC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC BTGGRPUPMPLZNT-PGEUSFDPSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241000209149 Zea Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 239000007866 anti-wear additive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
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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
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/38—Esters of polyhydroxy compounds
-
- 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
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/40—Esters containing free hydroxy or carboxyl groups
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
- C10M2207/2835—Esters of polyhydroxy compounds used as base material
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/2875—Partial esters used as base material
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10N2020/081—Biodegradable compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10N2030/02—Pour-point; Viscosity index
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10N2030/64—Environmental friendly compositions
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/30—Refrigerators lubricants or compressors lubricants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/32—Wires, ropes or cables lubricants
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/34—Lubricating-sealants
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/36—Release agents or mold release agents
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/38—Conveyors or chain belts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/40—Generators or electric motors in oil or gas winning field
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/42—Flashing oils or marking oils
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/44—Super vacuum or supercritical use
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/50—Medical uses
Definitions
- This invention is in the art of synthetic lubricants based on esters.
- TMP oleate trimethylolpropane trioleate
- TMP oleate is considered the industry standard in formulating biodegradable hydraulic fluids. It has the appropriate viscosity (circa 46 cst at 40° C.) and biodegradability.
- TMP oleate has poor oxidative and thermal stability, and poor low temperature fluidity (e.g., pour point). An effective replacement for TMP oleate has heretofore been unavailable.
- U.S. Pat. Nos. 5,658,863; 5,681,800; 5,728,658; 5,767,047; and 5,817,607 are directed to biodegradable lubricants comprising, inter alia, esters derived from branched acids. These acids are based on propylene oligomers, which are not considered renewable natural products.
- esters prepared by esterifying linear acids with alcohols wherein both the acids and alcohols are derived from natural products, provide lubricants having good biodegradability and eco-toxicity requirements, as well as technical requirements that are similar to or even superior to lubricants currently used by equipment manufacturers.
- an ester made by reacting sorbitol with 3-6 molar equivalents of a mixture of at least two different fatty acids provides a lubricant equal to or superior to TMP oleate.
- Sorbitol can be derived from natural products such as corn oil (hydrogenation of glucose) and certain linear fatty acids are derived from natural products such as coconut oil.
- a polyol derived from natural sources is partially or fully esterified with at least two different linear acids derived from natural sources (e.g., renewable), preferably two or more different fatty acids, each independently having from 6 to 12 carbon atoms, still more preferably two different linear fatty acids selected from C6, C8, C10, and C12 fatty acids. It is preferred that sorbitol is esterified with 3-6 molar equivalents of the mixed fatty acids.
- the term “mixed” means at least two fatty acids having different carbon number. Three or more different fatty acids may also be used. Examples of suitable acids include, but are not limited to, caprylic acid, capric acid, and lauric acid.
- a sorbitol ester fluid was made by refluxing 1.25 moles of sorbitol with 5.5 moles of a commercially available 60:40 wt % mixture of caprylic acid/capric acid (C8 and C10, respectively) at 240° C. The reaction proceeded until the hydroxyl number was less than 3. The hydroxyl number can be determined by one of skill in the art. Unreacted acids were removed by vacuum distillation. A further reduction in acidity was obtained by neutralizing the free acid with Ca(OH)2 until the total acid number (TAN), as determined by ASTM D974, was less than 0.1. The properties of this ester fluid are compared with TMP oleate in Table 1, below.
- Viscosity was determined according to ASTM D445. Pour point is determined according to ASTM D97. Flash point is determined according to ASTM D92.
- the stability of the oil based on the sorbitol ester fluid is superior to the oil based on the oleate ester.
- This is shown in the dry TOST test (Modified ASTM D943) and the oxidation and corrosion test.
- the TOST test is modified from the published method D943 in that no water is included in the test.
- the oxidation and corrosion test is according to FTM 5308, modified in that only copper, aluminum, and steel are used as metal specimens.
- the TOST life is reported in hours to achieve a TAN of greater than 2.
- the oil based on TMP oleate lasted 332 hours while the oil based on the sorbitol ester lasted more than 1000 hours.
- the demulsibility test is run according to ASTM D1401. 40 mls of oil and 40 mls of water are mixed in a graduated cylinder and held at 180° F. The amount of time for the oil and water to separate is recorded. The sorbitol ester separated water faster than the TMP oleate, which is beneficial in wet hydraulic systems.
- Foaming is measured by ASTM D892. Air is blown through a porous stone into a cylinder of oil. The volume of foam produced and the time required for the foam to collapse is recorded.
- the present invention is directed to an hydraulic oil formulated using an ester lubricant based on polyols and fatty acids derived from natural products, preferably an ester derived by esterifying sorbitol with a mixture of at least two linear fatty acids, even more preferably wherein the at least two linear acids are independently selected from acids having from 6 to 12 carbon atoms, and most preferably wherein the acids mixture comprises caprylic acid [CH3(CH2)6COOH] and capric acid [CH3(CH2)8COOH].
- the polyol most preferably sorbitol, can be esterified using at least 3 molar equivalents of total acids in the linear fatty acid mixture, preferably at least 4 molar equivalents of total acids in the linear fatty acid mixture, and more preferably at least 5 molar equivalents of total acids in the linear fatty acid mixture (equivalents based on the number of hydroxyl groups in the polyol). It can be esterified using less than 4 molar equivalents of mixed linear fatty acids (i.e., less than four alcohol groups esterified) or more than 4 molar equivalents, up to fully esterified.
- the hydraulic oil according to the present invention is preferably used in environmentally sensitive applications such as forestry, mining, and agriculture.
- a lubricant formulation having an ester as the base material comprising making said ester by reacting sorbitol with 3 to 6 molar equivalents of mixed linear fatty acids; or more preferably wherein said mixed linear fatty acids are selected from C6 to C12 acids; or even more preferably wherein said mixed linear fatty acids are selected from C6, C8, C10, and C12 acids; or still more preferably wherein said mixed linear fatty acids are caprylic and capric acids; yet still more preferably wherein said base material is made by reacting sorbitol with a 60:40 wt % mixture of caprylic and capric acids.
- the present invention is directed to:
- An hydraulic fluid for equipment used in forestry, mining, or agricultural operations comprising a base stock consisting essentially of an ester derived from natural products; more preferably wherein said ester is made esterifying at least one linear acid derived from corn with linear alcohols derived from coconut oil.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention relates to synthetic esters made from materials which can be derived from renewable resources.
Description
- This application claims priority to U.S. Provisional Application No. 60/291,816, filed May 17, 2001.
- This invention is in the art of synthetic lubricants based on esters.
- There is a concern over the biodegradability and other eco-toxicity properties of lubricants used in environmentally sensitive applications such as forestry, mining, and agriculture. Equipment manufacturers who use these lubricants have observed that product performance declines when so-called “biodegradable” based fluids are used. In addition to the environmentally friendly qualities such as biodegradability, recent regulatory initiatives are directed to using fluids derived from renewable resources (e.g., from agricultural products).
- TMP oleate (trimethylolpropane trioleate) is considered the industry standard in formulating biodegradable hydraulic fluids. It has the appropriate viscosity (circa 46 cst at 40° C.) and biodegradability. However, TMP oleate has poor oxidative and thermal stability, and poor low temperature fluidity (e.g., pour point). An effective replacement for TMP oleate has heretofore been unavailable.
- U.S. Pat. Nos. 5,658,863; 5,681,800; 5,728,658; 5,767,047; and 5,817,607 are directed to biodegradable lubricants comprising, inter alia, esters derived from branched acids. These acids are based on propylene oligomers, which are not considered renewable natural products.
- Recently French Patent Application 2,763,597 (A1) described a lubricating oil composition for using industrial materials used in the preparation of products intended for living biological organisms, e.g., food preparation. The reference does not address lubricating oils having the appropriate properties to replace TMP oleate.
- Thus there is a need for a fluid having the appropriate technical properties required by a lubricant while at the same time having environmentally friendly properties and being derived from renewable resources.
- The present inventor has found that esters prepared by esterifying linear acids with alcohols, wherein both the acids and alcohols are derived from natural products, provide lubricants having good biodegradability and eco-toxicity requirements, as well as technical requirements that are similar to or even superior to lubricants currently used by equipment manufacturers. In particular, an ester made by reacting sorbitol with 3-6 molar equivalents of a mixture of at least two different fatty acids provides a lubricant equal to or superior to TMP oleate.
- Sorbitol can be derived from natural products such as corn oil (hydrogenation of glucose) and certain linear fatty acids are derived from natural products such as coconut oil.
- These and other objects, features, and advantages of the present invention will become apparent as reference is made to the following detailed description of the preferred embodiments, specific examples, and the attached claims.
- A polyol derived from natural sources, preferably sorbitol, is partially or fully esterified with at least two different linear acids derived from natural sources (e.g., renewable), preferably two or more different fatty acids, each independently having from 6 to 12 carbon atoms, still more preferably two different linear fatty acids selected from C6, C8, C10, and C12 fatty acids. It is preferred that sorbitol is esterified with 3-6 molar equivalents of the mixed fatty acids. As used herein the term “mixed” means at least two fatty acids having different carbon number. Three or more different fatty acids may also be used. Examples of suitable acids include, but are not limited to, caprylic acid, capric acid, and lauric acid.
- A sorbitol ester fluid was made by refluxing 1.25 moles of sorbitol with 5.5 moles of a commercially available 60:40 wt % mixture of caprylic acid/capric acid (C8 and C10, respectively) at 240° C. The reaction proceeded until the hydroxyl number was less than 3. The hydroxyl number can be determined by one of skill in the art. Unreacted acids were removed by vacuum distillation. A further reduction in acidity was obtained by neutralizing the free acid with Ca(OH)2 until the total acid number (TAN), as determined by ASTM D974, was less than 0.1. The properties of this ester fluid are compared with TMP oleate in Table 1, below.
TABLE 1 Comparison of Esters TMP oleate Sorbitol caprylate/caprate Viscosity at 100° C., cSt 9.4 7.5 Viscosity at 40° C., cSt 48.0 48.1 Pour point, ° C. −42 −48 Flash pt, ° C. >310 272 Biodegradability, % by OECD 81 83 method 301B - Viscosity was determined according to ASTM D445. Pour point is determined according to ASTM D97. Flash point is determined according to ASTM D92.
- As shown in Table 1, the properties of the ester fluid according to the present invention are similar with respect to the technical aspects of the industry standard TMP oleate, but having an improved biodegradability and pour point.
- An ISO VG 46 hydraulic oil (meaning that the oil has a viscosity of 46 centistokes, or “46 cSt” at 40° C.) was blended with a standard additive package (Rhein Chemie RC 9308) containing rust inhibitor, anti-oxidants, and an anti-wear additive, with the sorbitol ester fluid as the base stock. A comparative formulation was made in the same way but using TMP oleate as the base stock. A comparison of the two compositions is shown below in Table 2.
TABLE 2 Comparison of Formulated Hydraulic Fluid Target TMP oleate Sorbitol caprylate/caprate Dry TOST, hours 500 minimum 332 1000+ Oxidation @ 175° C./72 hr % Viscosity increase 25 max. 219 5.9 TAN increase 2 max. 2 0.3 ASTM D665 rust A & B Pass Pass Pass Demulsibility, (ASTM D1401) 40 max. 20 15 minutes Foam by ASTM D892, mls/ 15/0 max. 10/0 10/0 mls - As shown in the table above, the stability of the oil based on the sorbitol ester fluid is superior to the oil based on the oleate ester. This is shown in the dry TOST test (Modified ASTM D943) and the oxidation and corrosion test. The TOST test is modified from the published method D943 in that no water is included in the test. The oxidation and corrosion test is according to FTM 5308, modified in that only copper, aluminum, and steel are used as metal specimens. The TOST life is reported in hours to achieve a TAN of greater than 2. The oil based on TMP oleate lasted 332 hours while the oil based on the sorbitol ester lasted more than 1000 hours.
- In the oxidation and corrosion test, an oil sample is held for 72 hours at 175° C. in the presence of copper, steel, and aluminum specimen. Air is sparged through the sample at a rate of 5 liter/hr. The change in TAN and viscosity are reported at the completion of the test. The viscosity increase of the oleate ester was about 35 time higher than the sorbitol ester, and the TAN increase was about 4 times higher. These performance features are useful to prolong the service life of ester based hydraulic fluids.
- The demulsibility test is run according to ASTM D1401. 40 mls of oil and 40 mls of water are mixed in a graduated cylinder and held at 180° F. The amount of time for the oil and water to separate is recorded. The sorbitol ester separated water faster than the TMP oleate, which is beneficial in wet hydraulic systems.
- Foaming is measured by ASTM D892. Air is blown through a porous stone into a cylinder of oil. The volume of foam produced and the time required for the foam to collapse is recorded.
- The present invention is directed to an hydraulic oil formulated using an ester lubricant based on polyols and fatty acids derived from natural products, preferably an ester derived by esterifying sorbitol with a mixture of at least two linear fatty acids, even more preferably wherein the at least two linear acids are independently selected from acids having from 6 to 12 carbon atoms, and most preferably wherein the acids mixture comprises caprylic acid [CH3(CH2)6COOH] and capric acid [CH3(CH2)8COOH]. The polyol, most preferably sorbitol, can be esterified using at least 3 molar equivalents of total acids in the linear fatty acid mixture, preferably at least 4 molar equivalents of total acids in the linear fatty acid mixture, and more preferably at least 5 molar equivalents of total acids in the linear fatty acid mixture (equivalents based on the number of hydroxyl groups in the polyol). It can be esterified using less than 4 molar equivalents of mixed linear fatty acids (i.e., less than four alcohol groups esterified) or more than 4 molar equivalents, up to fully esterified. The hydraulic oil according to the present invention is preferably used in environmentally sensitive applications such as forestry, mining, and agriculture.
- The invention has been described above with particular attention to the most preferred embodiments, but it will be appreciated by one of ordinary skill in the art in possession of the present disclosure that many variations and modifications of the aforementioned may be practiced within the spirit and scope of the appended claims. Those particular preferred embodiments include:
- A lubricant formulation having an ester as the base material, the improvement comprising making said ester by reacting sorbitol with 3 to 6 molar equivalents of mixed linear fatty acids; or more preferably wherein said mixed linear fatty acids are selected from C6 to C12 acids; or even more preferably wherein said mixed linear fatty acids are selected from C6, C8, C10, and C12 acids; or still more preferably wherein said mixed linear fatty acids are caprylic and capric acids; yet still more preferably wherein said base material is made by reacting sorbitol with a 60:40 wt % mixture of caprylic and capric acids.
- In another preferred embodiment, the present invention is directed to:
- An hydraulic fluid for equipment used in forestry, mining, or agricultural operations comprising a base stock consisting essentially of an ester derived from natural products; more preferably wherein said ester is made esterifying at least one linear acid derived from corn with linear alcohols derived from coconut oil.
Claims (7)
1. A lubricant formulation having an ester as the base material, the improvement comprising making said ester by reacting sorbitol with 3 to 6 molar equivalents of mixed linear fatty acids.
2. The lubricant formulation according to claim 1 , wherein said mixed linear fatty acids are selected from C6 to C12 acids.
3. The lubricant formulation according to claim 1 , wherein said mixed linear fatty acids are selected from C6, C8, C10, and C12 acids.
4. The lubricant formulation according to claim 1 , wherein said mixed linear fatty acids are caprylic and capric acids.
5. The lubricant formulation according to claim 1 , wherein said base material is made by reacting sorbitol with a 60:40 wt % mixture of caprylic and capric acids.
6. A hydraulic fluid for equipment used in forestry, mining, or agricultural operations comprising a base stock consisting essentially of an ester derived from natural products.
7. The hydraulic fluid according to claim 6 , wherein said ester is made esterifying at least one linear acid derived from coconut oil with a linear alcohol derived from corn.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/146,124 US20030004071A1 (en) | 2001-05-17 | 2002-05-15 | Biodegradable synthetic lubricants |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29181601P | 2001-05-17 | 2001-05-17 | |
| US10/146,124 US20030004071A1 (en) | 2001-05-17 | 2002-05-15 | Biodegradable synthetic lubricants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20030004071A1 true US20030004071A1 (en) | 2003-01-02 |
Family
ID=23121965
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/146,124 Abandoned US20030004071A1 (en) | 2001-05-17 | 2002-05-15 | Biodegradable synthetic lubricants |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US20030004071A1 (en) |
| AU (1) | AU2002303357A1 (en) |
| WO (1) | WO2002092733A2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090088351A1 (en) * | 2007-09-27 | 2009-04-02 | Chevron U.S.A. Inc. | Production of Biofuels and Biolubricants From a Common Feedstock |
| US20180044606A1 (en) * | 2015-02-27 | 2018-02-15 | Idemitsu Kosan Co., Ltd. | Biodegradable lubricating oil composition |
| US12325821B2 (en) | 2022-07-12 | 2025-06-10 | Secure Specialty Chemicals Corp. | Lubricant blends and methods for improving lubricity of brine-based drilling fluids |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2709964A1 (en) * | 2008-01-29 | 2009-08-06 | The Procter & Gamble Company | A highly esterified oligosaccharide polyester lubricant for machinery |
| GB2553340A (en) * | 2016-09-02 | 2018-03-07 | Illinois Tool Works | Wire Rope lubricant |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI66899C (en) * | 1983-02-11 | 1984-12-10 | Kasvisoeljy Vaextolje Ab Oy | SMOERJMEDEL MED TRIGLYCERIDER SOM HUVUDKONPONENT |
| US5346724A (en) * | 1991-04-12 | 1994-09-13 | Nippon Oil Company, Ltd. | Oil and fat composition for lubricating food processing machines and use thereof |
| US5458794A (en) * | 1993-09-30 | 1995-10-17 | The Lubrizol Corporation | Lubricants containing carboxylic esters from polyhydroxy compounds, suitable for ceramic-containing engines |
| PT802962E (en) * | 1994-12-08 | 2002-08-30 | Exxonmobil Chem Patents Inc | USE OF A BIODEGRADAVEL BRANCH SYNTHETIC SYNTHETIC MATERIAL IN A TWO-TIME ENGINE OIL IN ORDER TO REDUCE SMOKE PRODUCTION IN TWO ARRESTED AIR |
| US5665686A (en) * | 1995-03-14 | 1997-09-09 | Exxon Chemical Patents Inc. | Polyol ester compositions with unconverted hydroxyl groups |
| US5710030A (en) * | 1995-09-13 | 1998-01-20 | Henkel Corporation | Process for preparing fuels, fuel substitutes, and fuel supplements from renewable resources |
| FR2763597B1 (en) * | 1997-05-20 | 1999-12-17 | Igol Ind | LUBRICATING OIL COMPOSITION FORMED BY A BIODEGRADABLE AND NON-TOXIC SUGAR POLYESTER |
| CA2388296A1 (en) * | 1999-10-15 | 2001-04-26 | Danisco Cultor America, Inc. | Method for the direct esterification of sorbitol with fatty acids |
-
2002
- 2002-04-16 WO PCT/US2002/011825 patent/WO2002092733A2/en not_active Ceased
- 2002-04-16 AU AU2002303357A patent/AU2002303357A1/en not_active Abandoned
- 2002-05-15 US US10/146,124 patent/US20030004071A1/en not_active Abandoned
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090088351A1 (en) * | 2007-09-27 | 2009-04-02 | Chevron U.S.A. Inc. | Production of Biofuels and Biolubricants From a Common Feedstock |
| US8124572B2 (en) * | 2007-09-27 | 2012-02-28 | Chevron U.S.A. Inc. | Production of biofuels and biolubricants from a common feedstock |
| US20180044606A1 (en) * | 2015-02-27 | 2018-02-15 | Idemitsu Kosan Co., Ltd. | Biodegradable lubricating oil composition |
| US12325821B2 (en) | 2022-07-12 | 2025-06-10 | Secure Specialty Chemicals Corp. | Lubricant blends and methods for improving lubricity of brine-based drilling fluids |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2002092733A2 (en) | 2002-11-21 |
| WO2002092733A3 (en) | 2003-03-20 |
| AU2002303357A1 (en) | 2002-11-25 |
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