US3250709A - Mixed salt lubricants containing asphalt to eliminate haze - Google Patents
Mixed salt lubricants containing asphalt to eliminate haze Download PDFInfo
- Publication number
- US3250709A US3250709A US393347A US39334764A US3250709A US 3250709 A US3250709 A US 3250709A US 393347 A US393347 A US 393347A US 39334764 A US39334764 A US 39334764A US 3250709 A US3250709 A US 3250709A
- Authority
- US
- United States
- Prior art keywords
- fatty acid
- alkaline earth
- earth metal
- percent
- molecular weight
- 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.)
- Expired - Lifetime
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- 239000000314 lubricant Substances 0.000 title claims description 36
- 150000003839 salts Chemical class 0.000 title claims description 35
- 239000010426 asphalt Substances 0.000 title claims description 29
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 45
- 239000000194 fatty acid Substances 0.000 claims description 45
- 229930195729 fatty acid Natural products 0.000 claims description 45
- 150000004665 fatty acids Chemical class 0.000 claims description 40
- 239000002270 dispersing agent Substances 0.000 claims description 28
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 21
- 239000002253 acid Substances 0.000 claims description 18
- -1 AMINO Chemical class 0.000 claims description 17
- 229920002367 Polyisobutene Polymers 0.000 claims description 17
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- 239000010688 mineral lubricating oil Substances 0.000 claims description 9
- 239000010802 sludge Substances 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 8
- 239000010687 lubricating oil Substances 0.000 claims description 7
- 239000012530 fluid Substances 0.000 claims description 6
- 150000005673 monoalkenes Chemical class 0.000 claims description 5
- 230000001050 lubricating effect Effects 0.000 claims description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 3
- 229920000768 polyamine Polymers 0.000 claims description 3
- 239000007859 condensation product Substances 0.000 claims description 2
- 239000001384 succinic acid Substances 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical class CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 22
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 239000000047 product Substances 0.000 description 9
- 229960000583 acetic acid Drugs 0.000 description 8
- 239000003760 tallow Substances 0.000 description 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 229910052791 calcium Inorganic materials 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 5
- 239000000920 calcium hydroxide Substances 0.000 description 5
- 235000011116 calcium hydroxide Nutrition 0.000 description 5
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 5
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 239000001639 calcium acetate Substances 0.000 description 3
- 235000011092 calcium acetate Nutrition 0.000 description 3
- 229960005147 calcium acetate Drugs 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 229920005652 polyisobutylene succinic anhydride Polymers 0.000 description 3
- YWWVWXASSLXJHU-AATRIKPKSA-N (9E)-tetradecenoic acid Chemical compound CCCC\C=C\CCCCCCCC(O)=O YWWVWXASSLXJHU-AATRIKPKSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 235000015278 beef Nutrition 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- YWWVWXASSLXJHU-UHFFFAOYSA-N 9E-tetradecenoic acid Natural products CCCCC=CCCCCCCCC(O)=O YWWVWXASSLXJHU-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 101500021084 Locusta migratoria 5 kDa peptide Proteins 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000001279 citrus aurantifolia swingle expressed oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- TXWRERCHRDBNLG-UHFFFAOYSA-N cubane Chemical compound C12C3C4C1C1C4C3C12 TXWRERCHRDBNLG-UHFFFAOYSA-N 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 235000021281 monounsaturated fatty acids Nutrition 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- CKQVRZJOMJRTOY-UHFFFAOYSA-N octadecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O CKQVRZJOMJRTOY-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004711 α-olefin Substances 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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/082—Inorganic acids or salts thereof containing nitrogen
- C10M2201/083—Inorganic acids or salts thereof containing nitrogen nitrites
-
- C—CHEMISTRY; METALLURGY
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- C—CHEMISTRY; METALLURGY
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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
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/122—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/22—Acids obtained from polymerised unsaturated acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
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- C—CHEMISTRY; METALLURGY
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- 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
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/062—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups bound to the aromatic ring
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl amines
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/086—Imides [having hydrocarbon substituents containing less than thirty carbon atoms]
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/12—Partial amides of polycarboxylic acids
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/26—Amines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/12—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of organic compounds, e.g. with PxSy, PxSyHal or PxOy
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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
- C10M2225/00—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2225/04—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of macromolecualr compounds not containing phosphorus in the monomers
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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
- C10M2225/00—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2225/04—Organic macromolecular compounds containing phosphorus as ingredients in lubricant compositions obtained by phosphorisation of macromolecualr compounds not containing phosphorus in the monomers
- C10M2225/041—Hydrocarbon polymers
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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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/08—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
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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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Definitions
- Fluid lubricants containing alkaline earth metal mixed salts have come into use for marine diesel cylinder lubrication because these mixed salts have good anti-wear and load-carrying abilities, in addition to their ability to neutralize-free acid.
- a fluid lubricant containing calcium mixed salts of acetic acid and C to C fatty acid made by coneutralizing the acids with lime was very successful commercially as a marine diesel lubricant. Haze was not a problem with this particular lubricant since the lubricant was opaque and any haze could not be seen.
- the calcium acetate salt primarily provided the anti-wear and loadcarrying properties, while the intermediate molecular weight, i.e.
- C to C fatty acid salt served primarily as a stabilizing and suspending agent for maintaining the calcium acetate suitably dispersed in the oil.
- their suspending power for the calcium acetate was not as great as desired, with the occasional result that some separation of oil and salt occurred in storage and in use, leading to plugged lines and valves. It was then found that these marine diesel lubricants could be further improved in their stability by using certain additives known as sludge dispersants for crankcase lubricating oils, particularly when using a highmolecular weight fatty acid in place of part or all of the intermediate molecular weight fatty acid.
- the present invention is based upon the discovery that the addition of asphalt to the aforesaid lubricant, and similar mixed salt lubricants, will eliminate the haze to thereby obtain a clear, bright product. It is not known why the asphalt is effective in removing and preventing haze. One possibility is that the high molecular weight asphalt components react chemically or physically with the colloidally suspended haze, and since the asphalt is United States Patent 0 "ice oil soluble, that it somehow carries the haze into solution, thereby giving a clear product.
- the asphalt for convenience in dissolving in the lubricant, is preferably used in the form of an asphaltic oil such as a residuum oil.
- asphaltic residuum oils generally have a viscosity of 210 F. of about 200 to 1350 SUS, and contain about 2 to 20 wt. percent of asphalt measured as Holde hard asphalt.
- Preferred residuum oils will have a viscosity of 210 F. of 250 to 1,000 SUS and contain 3 to 12 wt. percent of asphalt measured as Holde hard asphalt.
- Holde hard asphalt is that asphalt insoluble in 86 degree (API) naphtha.
- the asphaltic residuum oils can be obtained as residues -by distillation of asphaltic petroleum crude oils such as those of South America, e.g. Lagunillas; California, e.g. San Joaquin; or Mid-Continent crudes; etc.
- the asphaltic oil of the invention can also be prepared by cutting back asphalt with mineral oil. Natural asphalts, such as Trinidad, Bermudez, gilsonite, g-rahamite, and Cuban asphalt 'can also be used.
- the mixed salt lubricants of the invention will generally comprise a major amount of mineral lubricating oil and about 2.0 to 20.0 Wt. percent of alkaline earth metal mixed salts of low and higher molecularweight fatty acids, and about 0.1 to 7.0 wt. percent of a dispersant.
- the dispersant is for colloidally dispersing the insoluble low molecular Weight fatty acid salt so as to make a transparent lubricant.
- the lubricant will contain 4.0 to 12.0 wt. percent of the fatty acid salts and 0.3 to 2.0 wt. percent dispersant.
- the alkaline earth metal mixed salts will generally be a mixture of salts of about 2.0 to 8.0 molar proportion of low molecular weight acid per molar proportion of high molecular weight fatty acid. There may also be present salt of up to 5 molar proportions of intermediate molecular weight, e.g. C to- C fatty acid per molar proportion of said high molecular weight acid.
- the alkaline earth metal component of the mixed salts include calcium, barium, strontium and'magnesium, al-' though calcium is preferred.
- the fatty acids are coneutralized with alkaline earth metal base, e.g. a hydroxide, oxide or carbonate. Lime (calcium hydroxide) is preferred.
- the low molecular Weight fatty acid component of the mixed salt will include those of 2 to 4 carbon atoms such as acetic, propionic, etc. Acetic acid or its anhydride is preferred.
- Operable C to C fatty acids are capric, caproic, lauric, etc. These acids are usually commercially available as mixtures, e.g. coconut oil acid.
- the high molecular weight fatty acids are the C to C fatty .acids including tallow fatty acids, oleic, palmitoleic, gadoleic, erucic, arachidonic, myristoleic acid, etc.
- Thes fatty acids are usually derived from either animal or vegetable sources.
- commercial fatty acid derived from naturally occurring materials will contain both saturated and unsaturated acid.
- some commercial fatty acids will contain about 40 or even 60 wt. percent of saturated fatty acids,
- the dispersant is one of a class of materials used in lubricating oils, such as crankcase motor oils, to disperse sludge.
- phosphos-ulfurized olefins which are well known and are prepared by reacting an olefin or an olefin polymer with P S to form a material believed to be a dithiophos-phoric acid. More specifically, the phosphosul-furized olefins are generally prepared by reacting phosphorus pentasulfide with a polymer of a monoolefin, e.g.
- an alpha olefin having 2 to 6 carbon atoms, said polymer having a molecular weight in the range of 600 to 4,000 Staudinger, preferably 700 to 1400 Staudinger, for about 0.5 to hours at 150 to 600 F.
- P 8 treated polyisobutylene is particularly preferred.
- Preparation of these phosphosulfurized polyolefin-s is more fully described in US. Patent 2,875,188.
- the phosphosulfurized polyolefin can be used per se, or it can be first hydrolyzed, or it can be used in the form of its metal salt.
- Hydrolyzation is readily carried out by treating the phosphosulfurized polyolefin with steam to thereby increase the acidity o fthe phosphosulfurizcd polyolefin. This hydrolyzation technique and product is also well known in the art.
- sludge dispersants are amino alkyl phenols and their salts, such as those described in US. Patents 2,353,491; 2,459,112 and 3,036,003.
- a particularly preferred material of this type is prepared by reacting two moles of nonyl phenol with one mole of ethylene diamine and two moles of formaldehyde.
- Another recently developed sludge dispersant is polyisobutylene succinic anhydride wherein the isobutylene group has a molecular weight of about 700 to 1200, as well as polya-mine derivatives thereof, namely amic acids and imides obtained by reacting polyamines, for example tetraethylene pentamine, wit-h said aforesaid polyisobutylene succinic anhydride.
- polyamines for example tetraethylene pentamine, wit-h said aforesaid polyisobutylene succinic anhydride.
- An example of materials of this type is described in English Patent No. 922,831.
- Another dispersant is alkaline earth metal petroleum, or synthetic, alkyl aryl sulfonates of about 300 to 700 molecular weight.
- dispersants differ considerably from each other in their chemical composition, they are all characterized by their oil-solubility and their common physical ability to maintain small particles stably dispersed in oil. And for the purpose of this invention, the chemical nature of the dispersant does not appear important, rather it appears to be the physical ability of the dispersant to disperse the otherwise substantially oil-insoluble salt of the low molecular weight fatty acid in very fine or colloidal size particles, so as to make a transparent lubricant.
- dispersants are preferably present as the low molecular weight fatty acid salt is formed in situ in the lubricating oil, and if the dispersant is an acid, it can be simultaneously neutralized to metal salt along with the fatty acid, since the salt forms of the above-noted sludge dispersants are also effective as dispersants.
- the mixed salt lubricants will usually be prepared by coneutralizing the fatty acids in the presence of oil and dispersant, with the alkaline earth metal base, followed by dehydration at a temperature of about 250 to 350" F. If the dispersant is an acid, it will be converted into its salt form. For purposes of economy, concentrates containing salt of 10 to 40 wt. percent, usually to wt. percent, of the fatty acid mixture, will be first prepared and then later diluted with additional oil to form the final lubricant of the invention.
- the mixed salt lubricants frequently contain various other additives in amounts of 0.1 to 10.0 wt. percent, based on the weight of the finished lubricant.
- additives that can be used are corrosion inhibitors such as sodium nitrite, lanolin, wool grease stearine; antioxidants such as phenyl m-napthylamine; auxiliary extreme pressure agents; auxiliary antiwear agents; dyes; etc.
- Glacial Acetic Acid
- the phosphosulfurized polyisobutylene was prepared by reacting polyisobutylene of about I 800 molecular weight (Staudinger) with 15 wt. percent P 8 based on the weight of polyisobutylene, at about 425 F. for about 8 hours under a nitrogen atmosphere.
- Table I Tallow Fatty Acids Phosphosulfurized Polyiso- 4 butylene. Hydrated Lime Phenyl-u naphthyla-mine Mineral lubricating oil of 60 SUS viscosity at 210 F. Mineral lubricating oil of 78 SUS v'scosity at 210 F aesiduum on 5% asphalt) 0.00 0.10.
- the amounts of hydrated lime are such as to neutralize the acetic and tallow acid as well as the phosphosulfurized polyisobutylene which is converted to metal salt.
- polyisobutylene can be used in its non-salt form.
- Example I can be repeated by decreasing the amount of lime so it is just sufiicient to neutralize the acetic and tallow acids, correspondingly increasing the amount of oil and adding the phosphosulfurized polybutylene after the neutralization, or after dehydration and cooling of the lubricant.
- Example I can be repeated but replacing the phosphosulfurized polyisobutylene with an equal molar equivalent amount of polyisobutylene succinic anhydride wherein the polyisobutylene group has a molecular weight of 1100 and correspondingly adjusting the amount of lime and mineral oil so as to obtain a neutral product.
- Example I can be repeated but using in place the phosphosulfurized polyisobutylene, a mole equivalent amount of the reaction product of 2 moles of nonyl phenol with 1 mole of ethylene diamine and 2 moles of formaldehyde.
- the foregoing dispersants can be present either during the neutralization of the fatty acids which is the preferred method and wherein the dispersant is converted into the corresponding alkaline earth metal salt or the dispersant can be added after this neutralization.
- the purpose of the dispersant is to aid in dispersing the mixed salt so finely that the lubricant is transparent and, as long as this is achieved, the exact dispersant used or how it is used is not critical.
- the present invention resides in the discovery that small amounts of asphalt can be used to convert a hazy, transparent, fluid, mixed salt lubricant into a haze-free clear product.
- a haze-free transparent fluid lubricating composition comprising a major amount of mineral lubricating oil containing about 2 to 20 wt. percent of alkaline earth metal mixed salt of C to C fatty acid and C to C fatty acid in a relative molar ratio of about 2 to 8 molar equivalent proportions of said C to C fatty acid per mole equivalent of said C to C fatty acid, about 0.1 to 7.0 wt. percent of a lubricating oil sludge dispersant, and about .001 to 0.2 wt. percent of asphalt.
- alkaline earth metal salts of said acid condensation products of said acid and polyamine, and alkaline earth metal alkyl aryl sulfonates of about 300 to 700 molecular weight.
- a haze-free substantially transparent, lubricating composition comprising a major amount of mineral lubricating oil and within the range of about 2 to 20 wt. percent of alkaline earth metal mixed salt of C to C fatty acid and C to C fatty acid having a Wijs iodine number of about 35 to 110, in a relative mole ratio of about 2 to 8 molar equivalent proportion of said C to C fatty acid per mole equivalent of said C to C fatty acid and alkaline earth metal salt of about 0.1 to 7.0 wt.
- alkaline earth salt of phosphosulfurized polymer of a C to C monoolefin as a dispersant said polymer having a molecular weight of about 600 to 4,000 Staudinger, and about .001 to 0.2 wt. percent of asphalt.
- a haze-free substantially transparent fluid lubricating oil composition suitable for marine diesel cylinder lubrication comprising a major amount of mineral lubricating oil, about 4 to 12 wt. percent of calcium mixed salt of acetic acid and C to C fatty acid in a molar ratio of about 2 to 8 mole equivalent of acetic acid per mole equivalent of C to C fatty acid, and about 0.3 to 2.0 wt. percent of calcium salt of P treated polyisobutylene having a molecular weight of about 700 to 1400 Staudinger, and about .002 to .020 asphalt.
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Description
haze.
3 250 709 MIXED SALT LUBRICANTS CONTAINING ASPHALT T ELIMINATE HAZE Arnold J. Morway, Clark, N.J., and Ralph E. Darley,
Glen Buruie, Md., assiguors to Esso Research and Engineering Company, a corporation of Delaware No Drawing. Filed Aug. 31, 1964, Ser. No. 393,347
5 Claims. (Cl. 25232.7)
weight fatty acids and containing a small amount of asphalt to prevent haze.
Fluid lubricants containing alkaline earth metal mixed salts have come into use for marine diesel cylinder lubrication because these mixed salts have good anti-wear and load-carrying abilities, in addition to their ability to neutralize-free acid. For example, a fluid lubricant containing calcium mixed salts of acetic acid and C to C fatty acid made by coneutralizing the acids with lime, was very successful commercially as a marine diesel lubricant. Haze was not a problem with this particular lubricant since the lubricant was opaque and any haze could not be seen. In this prior lubricant, the calcium acetate salt primarily provided the anti-wear and loadcarrying properties, while the intermediate molecular weight, i.e. C to C fatty acid salt served primarily as a stabilizing and suspending agent for maintaining the calcium acetate suitably dispersed in the oil. However, due to the short chain length of the intermediate fatty acid salts, their suspending power for the calcium acetate was not as great as desired, with the occasional result that some separation of oil and salt occurred in storage and in use, leading to plugged lines and valves. It was then found that these marine diesel lubricants could be further improved in their stability by using certain additives known as sludge dispersants for crankcase lubricating oils, particularly when using a highmolecular weight fatty acid in place of part or all of the intermediate molecular weight fatty acid. This use of high molecular weight fatty acid, in combination with the surfactant effect of the sludge dispersant, can result in liquid lubricants of exceptional stability against sedimentation and separation, and which are transparent since the particle size of the. calcium acetate component is colloidal when made in the presence of the aforesaid sludge dispersant. However, these transparent lubricants are frequently hazy.- It is not known with certainty what causes the haze, although it is believed caused by water from the salt formation which is not removed by the normal dehydration of the lubricant, and which for some reason will not separate from the lubricant. This haze is objection-able since it frequently leads the consumer to mistakenly believe the product is inferior and thus presents a serious marketing handicap.
The present invention is based upon the discovery that the addition of asphalt to the aforesaid lubricant, and similar mixed salt lubricants, will eliminate the haze to thereby obtain a clear, bright product. It is not known why the asphalt is effective in removing and preventing haze. One possibility is that the high molecular weight asphalt components react chemically or physically with the colloidally suspended haze, and since the asphalt is United States Patent 0 "ice oil soluble, that it somehow carries the haze into solution, thereby giving a clear product.
Usually about .001 to 0.2 wt. percent, preferably .002 to .020 wt. percent, of asphalt will be added to the mixed salt lubricant to eliminate haze.
The asphalt, for convenience in dissolving in the lubricant, is preferably used in the form of an asphaltic oil such as a residuum oil. These asphaltic residuum oils generally have a viscosity of 210 F. of about 200 to 1350 SUS, and contain about 2 to 20 wt. percent of asphalt measured as Holde hard asphalt. Preferred residuum oils will have a viscosity of 210 F. of 250 to 1,000 SUS and contain 3 to 12 wt. percent of asphalt measured as Holde hard asphalt. Holde hard asphalt is that asphalt insoluble in 86 degree (API) naphtha.
The asphaltic residuum oils can be obtained as residues -by distillation of asphaltic petroleum crude oils such as those of South America, e.g. Lagunillas; California, e.g. San Joaquin; or Mid-Continent crudes; etc. The asphaltic oil of the invention can also be prepared by cutting back asphalt with mineral oil. Natural asphalts, such as Trinidad, Bermudez, gilsonite, g-rahamite, and Cuban asphalt 'can also be used.
The mixed salt lubricants of the invention will generally comprise a major amount of mineral lubricating oil and about 2.0 to 20.0 Wt. percent of alkaline earth metal mixed salts of low and higher molecularweight fatty acids, and about 0.1 to 7.0 wt. percent of a dispersant. The dispersant is for colloidally dispersing the insoluble low molecular Weight fatty acid salt so as to make a transparent lubricant. Preferably, the lubricant will contain 4.0 to 12.0 wt. percent of the fatty acid salts and 0.3 to 2.0 wt. percent dispersant.
The alkaline earth metal mixed salts will generally be a mixture of salts of about 2.0 to 8.0 molar proportion of low molecular weight acid per molar proportion of high molecular weight fatty acid. There may also be present salt of up to 5 molar proportions of intermediate molecular weight, e.g. C to- C fatty acid per molar proportion of said high molecular weight acid.
The alkaline earth metal component of the mixed salts include calcium, barium, strontium and'magnesium, al-' though calcium is preferred. Usually, the fatty acids are coneutralized with alkaline earth metal base, e.g. a hydroxide, oxide or carbonate. Lime (calcium hydroxide) is preferred.
The low molecular Weight fatty acid component of the mixed salt will include those of 2 to 4 carbon atoms such as acetic, propionic, etc. Acetic acid or its anhydride is preferred.
Operable C to C fatty acids are capric, caproic, lauric, etc. These acids are usually commercially available as mixtures, e.g. coconut oil acid.
Examples of the high molecular weight fatty acids are the C to C fatty .acids including tallow fatty acids, oleic, palmitoleic, gadoleic, erucic, arachidonic, myristoleic acid, etc. Thes fatty acids are usually derived from either animal or vegetable sources. In some cases, commercial fatty acid derived from naturally occurring materials will contain both saturated and unsaturated acid. For example, some commercial fatty acids will contain about 40 or even 60 wt. percent of saturated fatty acids,
with the remainder being principally mono-unsaturated fatty acid along with minor amounts of polyunsaturated Wijs iodine numbers of about 35 to 110, preferably 40 to 80, and saponi-fication numbers of 250 to 150, preferably 225 to 175 mg. KOH/ gm.
The dispersant is one of a class of materials used in lubricating oils, such as crankcase motor oils, to disperse sludge. One preferred type of these materials are the phosphos-ulfurized olefins, which are well known and are prepared by reacting an olefin or an olefin polymer with P S to form a material believed to be a dithiophos-phoric acid. More specifically, the phosphosul-furized olefins are generally prepared by reacting phosphorus pentasulfide with a polymer of a monoolefin, e.g. an alpha olefin, having 2 to 6 carbon atoms, said polymer having a molecular weight in the range of 600 to 4,000 Staudinger, preferably 700 to 1400 Staudinger, for about 0.5 to hours at 150 to 600 F. P 8 treated polyisobutylene is particularly preferred. Preparation of these phosphosulfurized polyolefin-s is more fully described in US. Patent 2,875,188. The phosphosulfurized polyolefin can be used per se, or it can be first hydrolyzed, or it can be used in the form of its metal salt. Hydrolyzation is readily carried out by treating the phosphosulfurized polyolefin with steam to thereby increase the acidity o fthe phosphosulfurizcd polyolefin. This hydrolyzation technique and product is also well known in the art.
Other useful sludge dispersants are amino alkyl phenols and their salts, such as those described in US. Patents 2,353,491; 2,459,112 and 3,036,003. A particularly preferred material of this type is prepared by reacting two moles of nonyl phenol with one mole of ethylene diamine and two moles of formaldehyde. Another recently developed sludge dispersant is polyisobutylene succinic anhydride wherein the isobutylene group has a molecular weight of about 700 to 1200, as well as polya-mine derivatives thereof, namely amic acids and imides obtained by reacting polyamines, for example tetraethylene pentamine, wit-h said aforesaid polyisobutylene succinic anhydride. An example of materials of this type is described in English Patent No. 922,831. Another dispersant is alkaline earth metal petroleum, or synthetic, alkyl aryl sulfonates of about 300 to 700 molecular weight.
While the preceding dispersants differ considerably from each other in their chemical composition, they are all characterized by their oil-solubility and their common physical ability to maintain small particles stably dispersed in oil. And for the purpose of this invention, the chemical nature of the dispersant does not appear important, rather it appears to be the physical ability of the dispersant to disperse the otherwise substantially oil-insoluble salt of the low molecular weight fatty acid in very fine or colloidal size particles, so as to make a transparent lubricant. These dispersants are preferably present as the low molecular weight fatty acid salt is formed in situ in the lubricating oil, and if the dispersant is an acid, it can be simultaneously neutralized to metal salt along with the fatty acid, since the salt forms of the above-noted sludge dispersants are also effective as dispersants.
The mixed salt lubricants will usually be prepared by coneutralizing the fatty acids in the presence of oil and dispersant, with the alkaline earth metal base, followed by dehydration at a temperature of about 250 to 350" F. If the dispersant is an acid, it will be converted into its salt form. For purposes of economy, concentrates containing salt of 10 to 40 wt. percent, usually to wt. percent, of the fatty acid mixture, will be first prepared and then later diluted with additional oil to form the final lubricant of the invention.
The mixed salt lubricants frequently contain various other additives in amounts of 0.1 to 10.0 wt. percent, based on the weight of the finished lubricant. Among additives that can be used are corrosion inhibitors such as sodium nitrite, lanolin, wool grease stearine; antioxidants such as phenyl m-napthylamine; auxiliary extreme pressure agents; auxiliary antiwear agents; dyes; etc.
The invention will be further understood by reference Glacial Acetic Acid;
to the following example which includes a preferred embodiment of the invention.
EXAMPLE I.PREPARATION OF CONCENTRATE A mixed salt concentrate was prepared having the following formulatino, wherein all percents are weight percents:
Percent Glacial acetic acid 22.35 Tallow fatty acid (beef tallow), sap. No. 195, Wijs iodine No. 55, ave. C chain 3.51 Phosphosulfurized polyisobutylene 3.40 Hydrated lime 14.63 Phenyla-naphthylamine 0.27 Mineral lubricating oil of SUS vicosity at The oil, tallow fatty acid, phosphosulfurized polyisobutylene, and hydrated lime were mixed together in a steam jacketed grease kettle. Then, acetic acid was slowly added over about a six hour period, while mixing and while keeping the temperature of the kettle contents below F. The resulting grease mixture was then heated to 300 F. in order to dehydrate said mixture. The product was then cooled to 250 F., where phenyla-naphthylamine was added, and was then further cooled to room temperature. Mixing was carried out during the entire process described above by cycling the kettle contents through 3 Charlotte colloidal mill and then back to the kettle.
The phosphosulfurized polyisobutylene was prepared by reacting polyisobutylene of about I 800 molecular weight (Staudinger) with 15 wt. percent P 8 based on the weight of polyisobutylene, at about 425 F. for about 8 hours under a nitrogen atmosphere.
18.525 parts of the concentrate were mixed with 81.456 parts of additional mineral lubricating oil of 78 SUS viscosity at 210 F. to thereby form a finished diesel engine cylinder lubricant containing no asphalt. The mixture was hazy. Then 0.10 part of a residuum oil which contained asphalt, was mixed into the lubricant, whereupon said lubricant became clear and free of haze. This residuum oil was obtained by distillation of Lagunillas asphaltic crude oil and had a viscosity of about 800 SUS at 210 F. and contained about 5 wt. percent of Holde hard asphalt.
The lubricant, with and without the asphalt-containing residiuum oil, and its properties are summarized in Table I which follows:
Table I Tallow Fatty Acids Phosphosulfurized Polyiso- 4 butylene. Hydrated Lime Phenyl-u naphthyla-mine Mineral lubricating oil of 60 SUS viscosity at 210 F. Mineral lubricating oil of 78 SUS v'scosity at 210 F aesiduum on 5% asphalt) 0.00 0.10.
roperties:
A earance Light Yellowish- Dark Brown pp Green, Hazy. Clear. SSUVisJlOO" F 1.3M
SSU Via/210 F Engler Vis. 50 C 18 Ash percent as CaSO4 Total Base No Centrifuge, percent Sediment As seen by the preceding table, the addition of 0.1% of residuum oil so as to incorporate 0.005% asphalt in the lubricant removed the haze and gave a clear product and also reduced the amount of sediment that separated when the lubricant was centrifuged. At the same time, there was substantially no other change in the lubricants properties except a darkening of color, which is not objectionable as long as a clear product is obtained.
In the preceding example the amounts of hydrated lime are such as to neutralize the acetic and tallow acid as well as the phosphosulfurized polyisobutylene which is converted to metal salt. polyisobutylene can be used in its non-salt form. To illustrate, Example I can be repeated by decreasing the amount of lime so it is just sufiicient to neutralize the acetic and tallow acids, correspondingly increasing the amount of oil and adding the phosphosulfurized polybutylene after the neutralization, or after dehydration and cooling of the lubricant.
As a further illustration of the invention, Example I can be repeated but replacing the phosphosulfurized polyisobutylene with an equal molar equivalent amount of polyisobutylene succinic anhydride wherein the polyisobutylene group has a molecular weight of 1100 and correspondingly adjusting the amount of lime and mineral oil so as to obtain a neutral product. Or Example I can be repeated but using in place the phosphosulfurized polyisobutylene, a mole equivalent amount of the reaction product of 2 moles of nonyl phenol with 1 mole of ethylene diamine and 2 moles of formaldehyde. As in the case of the phosphosulfurized polyisobutylene, the foregoing dispersants can be present either during the neutralization of the fatty acids which is the preferred method and wherein the dispersant is converted into the corresponding alkaline earth metal salt or the dispersant can be added after this neutralization. The purpose of the dispersant is to aid in dispersing the mixed salt so finely that the lubricant is transparent and, as long as this is achieved, the exact dispersant used or how it is used is not critical.
In summary, the present invention resides in the discovery that small amounts of asphalt can be used to convert a hazy, transparent, fluid, mixed salt lubricant into a haze-free clear product.
What is claimed is:
1. A haze-free transparent fluid lubricating composition comprising a major amount of mineral lubricating oil containing about 2 to 20 wt. percent of alkaline earth metal mixed salt of C to C fatty acid and C to C fatty acid in a relative molar ratio of about 2 to 8 molar equivalent proportions of said C to C fatty acid per mole equivalent of said C to C fatty acid, about 0.1 to 7.0 wt. percent of a lubricating oil sludge dispersant, and about .001 to 0.2 wt. percent of asphalt.
2. A lubricant according to claim 1, wherein said dis-' persant is selected from the group consisting of phosphosulfurized polymers of C to C monoolefins having a molecular weight of about 600 to 4,000 Staudinger, alkaline earth metal salts of said polymers, amino alkyl However, the phosphosulfurized phenols, alkaline earth metal salts of said amino alkyl phenols, polyisobutylene succinic acid having a polyisobutylene group of about 700 to 1200 molecular weight,-
alkaline earth metal salts of said acid, condensation products of said acid and polyamine, and alkaline earth metal alkyl aryl sulfonates of about 300 to 700 molecular weight.
3. A haze-free substantially transparent, lubricating composition comprising a major amount of mineral lubricating oil and within the range of about 2 to 20 wt. percent of alkaline earth metal mixed salt of C to C fatty acid and C to C fatty acid having a Wijs iodine number of about 35 to 110, in a relative mole ratio of about 2 to 8 molar equivalent proportion of said C to C fatty acid per mole equivalent of said C to C fatty acid and alkaline earth metal salt of about 0.1 to 7.0 wt. percent of alkaline earth salt of phosphosulfurized polymer of a C to C monoolefin as a dispersant, said polymer having a molecular weight of about 600 to 4,000 Staudinger, and about .001 to 0.2 wt. percent of asphalt.
4; A lubricating composition according to claim 3, wherein said alkaline earth metal is calcium, said C to C fatty acid is acetic acid, said G to C fatty acid is beef tallow acid, and said monoolefin is isobutylene.
5. A haze-free substantially transparent fluid lubricating oil composition suitable for marine diesel cylinder lubrication comprising a major amount of mineral lubricating oil, about 4 to 12 wt. percent of calcium mixed salt of acetic acid and C to C fatty acid in a molar ratio of about 2 to 8 mole equivalent of acetic acid per mole equivalent of C to C fatty acid, and about 0.3 to 2.0 wt. percent of calcium salt of P treated polyisobutylene having a molecular weight of about 700 to 1400 Staudinger, and about .002 to .020 asphalt.
References Cited by the Examiner UNITED STATES PATENTS 1,708,563 4/1929 Black et al 25259 X 2,104,097 1/1938 Pier et al 25259 X 2,353,491 7/ 1944 Oberright 25242.7 X 2,976,242 3/1961 Morway 25239 XR 3,125,521 3/1964 Detweiler et al. 25240.7 X
FOREIGN PATENTS 922,831 4/ 1963 Great Britain.
OTHER REFERENCES Cross: The Handbook of Petroleum, Asphalt and Natural Gas (1931), p. 524.
DANIEL E. WYMAN, Primary Examiner.
C. F. DEES, Assistant Examiner.
Claims (2)
1. A HAZE-FREE TRANSPARENT FLUID LUBRICATING COMPOSITION COMPRISING A MAJOR AMOUNT OF MINERAL LUBRICATING OIL CONTAINING ABOUT 2 TO 20 WT. PERCENT OF ALKALINE EARTH METAL MIXED SALT OF C2 TO C4 FATTY ACID AND C14 TO C30 FATTY ACID IN A RELATIVE MOLAR RATIO OF ABOUT 2 TO 8 MOLAR EQUIVALENT PROPORTIONS OF SAID C2 TO C4 FATTY ACID PER MOLE EQUIVALENT OF SAID C14 TO C30 FATTY ACID, ABOUT 0.1 TO 7.0 WT. PERCENT OF A LUBRICATING OIL SLUDGE DISPERSANT, AND ABOUT .001 TO 0.2 WT. PERCENT OF ASPHALT.
2. A LUBRICANT ACCORDING TO CLAIM 1, WHEREIN SAID DISPERSANT IS SELECTED FROM THE GROUP CONSISTING OF PHOSPHOSULFURIZED POLYMERS OF C2 TO C6 MONOOLEFINS HAVING A MOLECULAR WEIGHT OF ABOUT 600 TO 4,000 STAUDINGER, ALKALINE EARTH METAL SALTS OF SAID POLYMERS, AMINO ALKAYL PHENOLS, ALKALINE EARTH METAL SALTS OF SAID AMINO ALKYL PHENOLS, POLYISOBUTYLENE SUCCINIC ACID HAVING A POLYISOBUTYLENE GROUP OF ABOUT 700 TO 1200 MOLECULAR WEIGHT, ALKALINE EARTH METAL SALTS OF SAID ACID, CONDENSATION PRODUCTS OF SAID ACID AND POLYAMINE, AND ALKALINE EARTH METAL ALKYL ARYL SULFONATES OF ABOUT 300 TO 700 MOLECULAR WEIGHT.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US393347A US3250709A (en) | 1964-08-31 | 1964-08-31 | Mixed salt lubricants containing asphalt to eliminate haze |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US393347A US3250709A (en) | 1964-08-31 | 1964-08-31 | Mixed salt lubricants containing asphalt to eliminate haze |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3250709A true US3250709A (en) | 1966-05-10 |
Family
ID=23554319
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US393347A Expired - Lifetime US3250709A (en) | 1964-08-31 | 1964-08-31 | Mixed salt lubricants containing asphalt to eliminate haze |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3250709A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3437594A (en) * | 1966-11-25 | 1969-04-08 | Mobil Oil Corp | Alkaline earth metal carboxylate dispersions |
| US3793200A (en) * | 1970-07-13 | 1974-02-19 | Phillips Petroleum Co | Lubricating oil additives |
| US20040232051A1 (en) * | 2001-03-09 | 2004-11-25 | Ramesh Varadaraj | Low viscosity hydrocarbon oils by sonic treatment |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1708563A (en) * | 1926-10-13 | 1929-04-09 | Pan American Petroleum Company | Process of imparting fluorescence to oil |
| US2104097A (en) * | 1934-03-29 | 1938-01-04 | Ig Farbenindustrie Ag | Lubricating oils |
| US2353491A (en) * | 1944-01-14 | 1944-07-11 | Socony Vacuum Oil Co Inc | Lubricating oil composition |
| US2976242A (en) * | 1955-04-01 | 1961-03-21 | Exxon Research Engineering Co | Lubricating grease compositions |
| GB922831A (en) * | 1959-03-30 | 1963-04-03 | Lubrizol Corp | Metal-free lubricant additives |
| US3125521A (en) * | 1964-03-17 | Calcium mixed-salt lubricant stabilized |
-
1964
- 1964-08-31 US US393347A patent/US3250709A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3125521A (en) * | 1964-03-17 | Calcium mixed-salt lubricant stabilized | ||
| US1708563A (en) * | 1926-10-13 | 1929-04-09 | Pan American Petroleum Company | Process of imparting fluorescence to oil |
| US2104097A (en) * | 1934-03-29 | 1938-01-04 | Ig Farbenindustrie Ag | Lubricating oils |
| US2353491A (en) * | 1944-01-14 | 1944-07-11 | Socony Vacuum Oil Co Inc | Lubricating oil composition |
| US2976242A (en) * | 1955-04-01 | 1961-03-21 | Exxon Research Engineering Co | Lubricating grease compositions |
| GB922831A (en) * | 1959-03-30 | 1963-04-03 | Lubrizol Corp | Metal-free lubricant additives |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3437594A (en) * | 1966-11-25 | 1969-04-08 | Mobil Oil Corp | Alkaline earth metal carboxylate dispersions |
| US3793200A (en) * | 1970-07-13 | 1974-02-19 | Phillips Petroleum Co | Lubricating oil additives |
| US20040232051A1 (en) * | 2001-03-09 | 2004-11-25 | Ramesh Varadaraj | Low viscosity hydrocarbon oils by sonic treatment |
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