DE1258999B - Mineral or synthetic lubricating oil - Google Patents
Mineral or synthetic lubricating oilInfo
- Publication number
- DE1258999B DE1258999B DES89599A DES0089599A DE1258999B DE 1258999 B DE1258999 B DE 1258999B DE S89599 A DES89599 A DE S89599A DE S0089599 A DES0089599 A DE S0089599A DE 1258999 B DE1258999 B DE 1258999B
- Authority
- DE
- Germany
- Prior art keywords
- weight
- percent
- oil
- lubricating oil
- mineral
- 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.)
- Pending
Links
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims description 5
- 239000010688 mineral lubricating oil Substances 0.000 title claims description 5
- 239000010689 synthetic lubricating oil Substances 0.000 title claims description 5
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 claims description 8
- 229960005147 calcium acetate Drugs 0.000 claims description 8
- 235000011092 calcium acetate Nutrition 0.000 claims description 8
- 239000001639 calcium acetate Substances 0.000 claims description 8
- -1 sarcosine compound Chemical class 0.000 claims description 7
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 7
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N N-methylaminoacetic acid Natural products C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 235000007586 terpenes Nutrition 0.000 claims description 5
- VKCLPVFDVVKEKU-UHFFFAOYSA-N S=[P] Chemical compound S=[P] VKCLPVFDVVKEKU-UHFFFAOYSA-N 0.000 claims description 4
- 108010077895 Sarcosine Proteins 0.000 claims description 4
- 229940043230 sarcosine Drugs 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 19
- 239000010687 lubricating oil Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- 239000000654 additive Substances 0.000 description 13
- 239000000047 product Substances 0.000 description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 229910052791 calcium Inorganic materials 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- DIOYAVUHUXAUPX-KHPPLWFESA-N Oleoyl sarcosine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CC(O)=O DIOYAVUHUXAUPX-KHPPLWFESA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 239000001293 FEMA 3089 Substances 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- ONBMZSARMOMISG-UHFFFAOYSA-N 2,3-dioctylbenzenesulfonic acid Chemical compound CCCCCCCCC1=CC=CC(S(O)(=O)=O)=C1CCCCCCCC ONBMZSARMOMISG-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- AQQPJNOXVZFTGE-UHFFFAOYSA-N 2-octadecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O AQQPJNOXVZFTGE-UHFFFAOYSA-N 0.000 description 1
- QWHHBVWZZLQUIH-UHFFFAOYSA-N 2-octylbenzenesulfonic acid Chemical compound CCCCCCCCC1=CC=CC=C1S(O)(=O)=O QWHHBVWZZLQUIH-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- 239000013556 antirust agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical class [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229930006739 camphene Natural products 0.000 description 1
- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000011436 cob Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- SFMJNHNUOVADRW-UHFFFAOYSA-N n-[5-[9-[4-(methanesulfonamido)phenyl]-2-oxobenzo[h][1,6]naphthyridin-1-yl]-2-methylphenyl]prop-2-enamide Chemical compound C1=C(NC(=O)C=C)C(C)=CC=C1N1C(=O)C=CC2=C1C1=CC(C=3C=CC(NS(C)(=O)=O)=CC=3)=CC=C1N=C2 SFMJNHNUOVADRW-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
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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
- 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
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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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/024—Propene
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
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- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/17—Fisher Tropsch reaction products
- C10M2205/173—Fisher Tropsch reaction products used as base material
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
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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
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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
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/30—Complex esters, i.e. compounds containing at leasst three esterified carboxyl groups and derived from the combination of at least three different types of the following five types of compounds: monohydroxyl compounds, polyhydroxy xompounds, monocarboxylic acids, polycarboxylic acids or hydroxy carboxylic acids
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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
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
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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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated derivatives
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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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- 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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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/046—Overbased sulfonic acid salts
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/088—Neutral salts
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/089—Overbased salts
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- 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
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/02—Macromolecular compounds obtained by reactions of monomers involving only carbon-to-carbon unsaturated bonds
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- 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
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- 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
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- 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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- 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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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
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- C10N2040/253—Small diesel engines
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
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Description
DEUTSCHESGERMAN
PATENTAMTPATENT OFFICE
AUSLEGESCHRIFTEDITORIAL
Int. Cl.:Int. Cl .:
ClOmClOm
Deutsche Kl.: 23 c-1/01 German class: 23 c -1/01
Nummer: 1 258 999Number: 1 258 999
Aktenzeichen: S 89599IV c/23 cFile number: S 89599IV c / 23 c
Anmeldetag: 19. Februar 1964Filing date: February 19, 1964
Auslegetag: 18. Januar 1968Opening day: January 18, 1968
Die Erfindung bezieht sich/auf ein mineralisches oder synthetisches Schmieröl, das eine Mehrzahl von Schmierölzusätzen enthält.The invention relates to a mineral or synthetic lubricating oil comprising a plurality of Contains lubricating oil additives.
Die Verwendung der Einzelkomponenten als Schmierölzusätze ist hinreichend bekannt.The use of the individual components as lubricating oil additives is well known.
Es wurde nun gefunden, daß man eine besonders wertvolle Schmiermitteldispersion zum Schmieren von Schiffsdieselmaschinen erhält, wenn man dazu ein Schmieröl auf der Basis von mineralischen oder synthetischen Schmierölen mit einem Gehalt von 1 bis 20 Gewichtsprozent Calciumacetat, 0,01 bis 3 Gewichtsprozent einer N-acylsubstituierten Sarkosinverbindung der FormelIt has now been found that one can obtain a particularly valuable lubricant dispersion for lubrication from marine diesel engines, if you add a lubricating oil based on mineral or synthetic lubricating oils containing 1 to 20 percent by weight calcium acetate, 0.01 to 3 percent by weight of an N-acyl-substituted sarcosine compound of the formula
O
R — C — N — CH2 — COOHO
R - C - N - CH 2 - COOH
CH3 CH 3
worin R ein aliphatischer Kohlenwasserstoffrest mit 8 bis 24 Kohlenstoffatomen ist, 0,1 bis 10 Gewichtsprozent eines bekannten Metallsulfonats und 0,1 bis 5 Gewichtsprozent eines bekannten Reaktionsproduktes aus 1 Mol eines Phosphorsulfids mit 4 Mol eines dicyclischen Terpens verwendet.wherein R is an aliphatic hydrocarbon radical having 8 to 24 carbon atoms, 0.1 to 10 weight percent of a known metal sulfonate and 0.1 to 5 percent by weight of a known reaction product from 1 mole of a phosphorus sulfide with 4 moles of a dicyclic terpene used.
Diese Schmierölzusammensetzung verhindert die Bildung von Ablagerungen an den Zylinderdurchlässen oder Schlitzen, besitzt gute Lasttrageigenschaften, d. h. die Fähigkeit, hohen Drücken zu widerstehen, und neutralisiert die während der Verbrennung von hochschwefelhaltigen Brennstoffen in Dieselmaschinen gebildeten schwefelhaltigen Säuren.This lubricating oil composition prevents the formation of deposits on the cylinder passages or slitting, has good load bearing properties, i.e. H. the ability to handle high pressures too resist and neutralize the during the combustion of high sulfur fuels in Sulphurous acids formed by diesel engines.
Ein weiterer Vorteil der Mischung ist die äußerst niedrige Abnutzung von Maschinenteilen während des Betriebes der Schiffsdieselmaschinen.Another advantage of the mixture is the extremely low wear and tear on machine parts during the operation of marine diesel engines.
Das Calciumacetat wird bevorzugt in einer Menge von 2 bis 8 Gewichtsprozent, das Sarkosin von 0,1 bis 1, das Metallsulfonat von 1 bis 5 Gewichtsprozent und das Reaktionsprodukt von 1 bis 3 Gewichtsprozent verwendet.The calcium acetate is preferably in an amount of 2 to 8 percent by weight, the sarcosine of 0.1 to 1, the metal sulfonate from 1 to 5 percent by weight and the reaction product from 1 to 3 percent by weight used.
Die Gesamtmenge der Zusätze beträgt daher etwa 1 bis 35 Gewichtsprozent der Schmierölmenge. Bei Brennstoffen mit hohem Schwefelgehalt (1 bis 5% Schwefel) wird dem Schmieröl 15 bis 25 Gewichtsprozent Zusätze beigemischt.The total amount of additives is therefore about 1 to 35 percent by weight of the amount of lubricating oil. at Fuels with a high sulfur content (1 to 5% sulfur) add 15 to 25 percent by weight to the lubricating oil Additives mixed in.
Als Schmieröle werden naphthenbasische, paraffinbasische, coastalbasische und gemischtbasische öle, auch synthetische Kohlenwasserstofföle und andere synthetische öle, wie Alkylenoxydpolymerisate, Dicarbonsäureester, flüssige Ester von Phosphor, Polypropylenglykol verwendet. Die öle sollen eine Viskosität (S. U. S.) von mehr als 70 Sekunden Mineralisches oder synthetisches SchmierölThe lubricating oils used are naphthenic, paraffinic, coastal and mixed-basic oils, including synthetic hydrocarbon oils and other synthetic oils, such as alkylene oxide polymers, Dicarboxylic acid esters, liquid esters of phosphorus, polypropylene glycol are used. The oils should a viscosity (S.U. S.) greater than 70 seconds Mineral or synthetic lubricating oil
Anmelder:Applicant:
Mobil Oil Corporation,
New York, N. Y. (V. St. A.)Mobil Oil Corporation,
New York, NY (V. St. A.)
Vertreter:Representative:
Dr. E. Wiegand und Dipl.-Ing. W. Niemann,Dr. E. Wiegand and Dipl.-Ing. W. Niemann,
Patentanwälte,Patent attorneys,
8000 München 15, Nußbaumstr. 108000 Munich 15, Nussbaumstr. 10
Als Erfinder benannt:
Pierre Marie Coant, Woodbury, N. J.;
Francis George Augustine de Monterey,
Woodbury Heights, N. J. (V. St. A.)Named as inventor:
Pierre Marie Coant, Woodbury, NJ;
Francis George Augustine de Monterey,
Woodbury Heights, NJ (V. St. A.)
Beanspruchte Priorität:
V. St. v. Amerika vom 19. Februar 1963
(259 736)Claimed priority:
V. St. v. America 19 February 1963
(259 736)
bei 38 0C, vorzugsweise von 100 bis 2000 Sekunden bei 38° C besitzen. Sehr geeignet sind lösungsmittelraffinierte Coastalöle und Mischungen davon mit Viskositäten (S. U. S.) von 150 bis 700 Sekunden bei 38°C.hold at 38 0 C, preferably from 100 to 2,000 seconds at 38 ° C. Solvent-refined coastal oils and mixtures thereof with viscosities (SUS) of 150 to 700 seconds at 38 ° C are very suitable.
Das Calciumacetat kann wasserfrei oder hydratisiert sein.The calcium acetate can be anhydrous or hydrated.
Als N-acylsubstituierte Sarkosine werden folgende verwendet: N-Pelargonyl, N-Undecyloyl, N-Lauroyl, N-Myristoyl, N-Palmitoyl, N-Stearoyl, N-Oleoyl, N-Linoleoyl, N-Arachidoyl, N-Behenoyl, N-Hyenoyl. Oleylsarkosin wird bevorzugt.The following are used as N-acyl-substituted sarcosines: N-Pelargonyl, N-Undecyloyl, N-Lauroyl, N-myristoyl, N-palmitoyl, N-stearoyl, N-oleoyl, N-linoleoyl, N-arachidoyl, N-behenoyl, N-hyenoyl. Oleyl sarcosine is preferred.
Als Metallsulfonate werden bekannte Erdölsulfonsäuren und synthetische Alkarylsulfonsäuren, insbesondere diejenigen mit hohen Molekulargewichten, von 300 bis 800, wie Octylbenzolsulfonsäure, Dodecylbenzolsulfonsäure, Dioctylbenzolsulfonsäure, Octadecylbenzolsulfonsäure, Wachsbenzolsulfonsäure und Wachsnaphthalinsulfonsäure verwendet. Known petroleum sulfonic acids and synthetic alkaryl sulfonic acids, in particular, are used as metal sulfonates those with high molecular weights, from 300 to 800, such as octylbenzenesulfonic acid, Dodecylbenzenesulfonic acid, dioctylbenzenesulfonic acid, octadecylbenzenesulfonic acid, waxbenzenesulfonic acid and wax naphthalenesulfonic acid is used.
Als Metalle sind Calcium, Barium und Magnesium geeignet. Bevorzugt wird ein schwach basisches Calciumerdölsulfonat.Calcium, barium and magnesium are suitable metals. A weakly basic one is preferred Calcium petroleum sulfonate.
Das Reaktionsprodukt erhält man durch Umsetzung eines dicyclischen Terpens und eines Phosphorsulfids bei einer Temperatur von 100 bis 1600C.The reaction product obtained by reacting a di-cyclic terpene and a phosphorus sulfide at a temperature of 100 to 160 0 C.
709 719/389709 719/389
Die Phosphorsulfide umfassen ζ. B. P3S6,
P4S35PaS5, P4S7. P2S5 wird bevorzugt.The phosphorus sulfides include ζ. B. P3S6,
P 4 S 35 PaS 5 , P4S7. P2S5 is preferred.
Die dicyclischen Terpene sind solche, die eine Doppelbindung in dem Molekül enthalten und zwei Ringsysteme aufweisen. Beispiele sind Pinen, Camphen und Fenchen oder Gemische derselben. Auch ätherische öle, die vorwiegend ein solches Terpen enthalten, z. B. Terpentinöl, können verwendet werden. Bevorzugt sind Pinen und Terpentinöl. The dicyclic terpenes are those that contain a double bond in the molecule and have two ring systems. Examples are pinene, camphene and fenchen or mixtures thereof. Also essential oils that predominantly contain such a terpene, e.g. B. turpentine oil can be used will. Pinene and turpentine oil are preferred.
Zunächst wird getrennt eine stabilisierte ΌΊ-dispersion des Calciumacetats und Sarkosins in einem Manton-Gaulin-Homogenisator, der mit einem Druck von etwa 70 bis 350 kg/cm2 betrieben wird, durch Mischen hergestellt. Anschließend werden dann die anderen Zusätze der stabilisierten Dispersion bei 20 bis 1000C, vorzugsweise 90 bis 1000C, zugegeben.First, a stabilized ΌΊ-dispersion of calcium acetate and sarcosine is produced separately by mixing in a Manton-Gaulin homogenizer, which is operated at a pressure of about 70 to 350 kg / cm 2. The other additives are then added to the stabilized dispersion at from 20 to 100 ° C., preferably from 90 to 100 ° C.
Beispiel 5 Erfindungsgemäßes Schmierölgemisch ausExample 5 Lubricating oil mixture according to the invention from
Lösungsmittelraffiniertes CoastalölSolvent refined coastal oil
55 bis 60 S. U. S. bei 99° C 55 to 60 S. U.S. at 99 ° C
150 bis 160 S. U. S. bei 99°C 150 to 160 S.U. S. at 99 ° C
Produkt aus Beispiel 1 Product from example 1
Produkt aus Beispiel 3 Product from example 3
Produkt aus Beispiel 4 Product from example 4
TeileParts
7878
5 145 14
2020th
57 Teile Mineralöl, 40 Teile Calciumacetat und 3 Teile Oleoylsarkosin werden in einen Mischkessel eingebracht. Die Mischung wird unter Rühren auf 138 0C erhitzt, 20 Minuten lang bei dieser Temperatur gehalten und dann auf 25 0C abgekühlt. Sodann wird mittels eines Manton-Gaulin-Homogenisators (210 kg/cm2) homogenisiert.57 parts of mineral oil, 40 parts of calcium acetate and 3 parts of oleoyl sarcosine are placed in a mixing vessel. The mixture is heated to 138 ° C. with stirring, kept at this temperature for 20 minutes and then cooled to 25 ° C. It is then homogenized using a Manton-Gaulin homogenizer (210 kg / cm 2 ).
Das verwendete Mineralöl bestand aus einem lösungsmittelraffinierten naphthenischen Coastalöl mit einer Viskosität (S. U. S.) von 500 Sekunden bei 38°C. Das Calciumacetat enthielt 6% Wasser.The mineral oil used consisted of a solvent-refined naphthenic coastal oil having a viscosity (S.U. S.) of 500 seconds at 38 ° C. The calcium acetate contained 6% water.
Destillat von einer Viskosität (S. U. S.) von 95 Sekunden bei 38° C wird mit Oleum behandelt, dann gefiltert und mit Ätznatronlösung neutralisiert. Die Mischung von öl und Natriumsulfonaten wird dann mit einer wäßrigen Lösung von Bariumchloriden umgesetzt. Nach Abtrennung der ölschicht und Trocknen erhält man ein Bariumerdölsulfonat. Distillate with a viscosity (S.U. S.) of 95 seconds at 38 ° C is treated with oleum, then filtered and neutralized with caustic soda solution. The mixture of oil and sodium sulfonates is made then reacted with an aqueous solution of barium chlorides. After separation of the oil layer and drying gives a barium petroleum sulfonate.
Mineralöl eines schwach basischen Calciumerdölsulfonats (etwa 40% aktiver Bestandteil) der Eigenschaften :Mineral oil of a weakly basic calcium petroleum sulfonate (about 40% active ingredient) of the properties :
Dichte, 0API 15,6Density, 0 API 15.6
Flammpunkt, 0C 243Flash point, 0 C 243
Viskosität (S. U. S.), 99°C, Sekunden 1100Viscosity (S.U. S.), 99 ° C, 1100 seconds
Calcium, Gewichtsprozent 1,7Calcium, weight percent 1.7
Schwefel, Gewichtsprozent 2,7Sulfur, weight percent 2.7
Basenzahl 8,0Base number 8.0
800 Gewichtsteile Pinen und ein gleiches Gewicht von Motoröl, Viskosität (S. U. S.) 45 Sekunden bei 99°C, werden auf 105°C unter Rühren erhitzt. Es werden langsam 326 Teile P2S5 zugegeben, wobei die Temperatur infolge der exothermen Reaktion auf 115°C steigt. Die Mischung wird erhitzt und filtriert. Das Filtrat, das aus 1842 Gewichtsteilen besteht, wird dann im Vakuum bei 5 mm Druck auf eine Gefäßtemperatur von 1500C getoppt. Der Rückstand der aus 1693 Gewichtsteilen besteht, ist ein klares viskoses öl.800 parts by weight of pinene and an equal weight of motor oil, viscosity (SUS) 45 seconds at 99 ° C, are heated to 105 ° C with stirring. 326 parts of P2S5 are slowly added, the temperature rising to 115 ° C. as a result of the exothermic reaction. The mixture is heated and filtered. The filtrate, consisting of 1842 parts by weight, is then topped off under vacuum at 5 mm pressure to a pot temperature of 150 0 C. The residue, which consists of 1693 parts by weight, is a clear, viscous oil.
Das öl wird bei 900C 2 Stunden innig gemischt. Das öl hat folgende Eigenschaften:The oil is intimately mixed at 90 ° C. for 2 hours. The oil has the following properties:
Dichte, 0API 21,5Density, 0 API 21.5
S. U. S., 38°C 1242S. U.S., 38 ° C 1242
S. U. S., 99°C 95S.U. S., 99 ° C 95
Viskositätsindex 88Viscosity Index 88
Gesamtbasenzahl (TBN) 40Total Base Number (TBN) 40
Beispiel 6 Erfindungsgemäßes Schmierölgemisch ausExample 6 Lubricating oil mixture according to the invention from
Teile 70Part 70
Paraffinisches Destillatneutralöl
46,5 S. U. S., bei 99°C Paraffinic distillate neutral oil
46.5 SUS, at 99 ° C
NeutralölNeutral oil
90S. U. S. 990C 1390S. US 99 0 C 13
Produkt nach Beispiel 1 14Product according to example 1 14
Produkt nach Beispiel 3 2Product according to example 3 2
Produkt nach Beispiel 4 1Product according to example 4 1
Die Komponenten werden bei 82°C gerührt. Die Eigenschaften des Schmieröles sind:The components are stirred at 82 ° C. the Properties of the lubricating oil are:
Dichte, 0API 22,0Density, 0 API 22.0
S. U. S., 38°C 1200S. U.S., 38 ° C 1200
S. U. S., 99°C 95S.U. S., 99 ° C 95
Gesamtbasenzahl (TBN) 40Total Base Number (TBN) 40
Bei Anwendung des Schmieröls gemäß der Erfindung wird, wie Vergleichsversuche zeigten, ein synergistischer Effekt erzielt. Bei diesen Versuchen wurde das »Almen Load«-Prüfverfahren befolgt, .um die Lasttragfähigkeit eines Getriebeschmiermittels für Hochdruckschmierung zu bestimmen. Die Almenmaschine besteht aus einem Stift, der zwischen Buchsen umläuft, die steigend in periodischen Zeiträumen belastet werden, bis ein Anfressen oder ein Ausfall zwischen dem Stift und den Buchsen eintritt. Die Ablesungen bei Ausfall werden in Einheiten entsprechend englischen Pfund angegeben und sind Mittelwerte von zwei getrennten Versuchen.When using the lubricating oil according to the invention, as comparative tests showed, a synergistic effect achieved. The "Almen Load" test procedure was followed in these tests, . to determine the load-bearing capacity of a gear lubricant for high pressure lubrication. The Almenmaschine consists of a pin that revolves between sockets that rise in periodic intervals Periods of time are charged until a seizure or failure between the pin and the sockets entry. Failure readings are given in units equivalent to English pounds and are the mean values of two separate experiments.
Die zu prüfenden Schmiermittel wurden aus einem lösungsmittelraffinierten Mineralöl und verschiedenen Mengen der folgenden Zusätze hergestellt:The lubricants to be tested were made from a solvent-refined mineral oil and various Quantities of the following additives made:
A. der Calciumacetat-Oleylsarkosindispersion gemäß Beispiel 1,A. the calcium acetate oleyl sarcosine dispersion according to Example 1,
B. einer Calciumerdölsulfonatlösung, hergestellt gemäß Beispiel 3 undB. a calcium petroleum sulfonate solution, prepared according to Example 3 and
C. dem PiiSs-Pinenreaktionsprodukt, hergestellt gemäß Beispiel 4.C. the PiiSs pinene reaction product, prepared according to Example 4.
Die Ergebnisse der »Almen Load«-Prüfung sind nachstehend in Tabellenform zusammengefaßt. Die Zusammensetzungen jedes der geprüften Schmieröle sind ebenfalls in der Tabelle angegeben. Die Zusammensetzung des Schmieröles Nr. 8 ist ähnlich derjenigen der Beispiele 5 und 6.The results of the "Almen Load" test are summarized below in tabular form. the Compositions of each of the lubricating oils tested are also given in the table. The composition No. 8 lubricating oil is similar to that of Examples 5 and 6.
314th
3
214th
2
80003
8000
80003
8000
45001
4500
140001
14000
Anfreßlast, Einheiten "Almen Load" test
Seizure load, units
Die Zusammensetzungen 1 bis 7, bestehend aus öl allein, dem öl mit den einzelnen Zusätzen und dem öl mit zwei kombinierten Zusätzen, zeigten alle Ausfall bei Belastungen unter 10 000 Einheiten. Das Schmieröl 8 hatte jedoch eine maximale Belastbarkeit von 14 000 Einheiten bei einer Gesamtzusatzstoffkonzentration, die nicht größer als diejenige bei den Zusammensetzungen 2, 5 und 6 war.The compositions 1 to 7, consisting of oil alone, the oil with the individual additives and the oil with two combined additives, all showed failure at loads below 10,000 units. That However, lubricating oil 8 had a maximum load capacity of 14,000 units at a total additive concentration which was no greater than that of compositions 2, 5 and 6.
Dem beanspruchten Schmierölgemisch können auch noch andere übliche Zusätze, wie Fließpunkterniedriger, Viskositätsindexverbesserer, Antirostmittel, Reinigungsmittel oder Entschäumer beigemischt werden.Other customary additives, such as pour point depressants, Viscosity index improvers, anti-rust agents, cleaning agents or defoamers added will.
Claims (1)
Deutsche Patentschrift Nr. 856 773.Considered publications:
German patent specification No. 856 773.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US259736A US3259577A (en) | 1963-02-19 | 1963-02-19 | Lubricant and additives therefor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1258999B true DE1258999B (en) | 1968-01-18 |
Family
ID=22986151
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DES89599A Pending DE1258999B (en) | 1963-02-19 | 1964-02-19 | Mineral or synthetic lubricating oil |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3259577A (en) |
| DE (1) | DE1258999B (en) |
| GB (1) | GB1023710A (en) |
| NL (1) | NL6401443A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3488721A (en) * | 1967-06-12 | 1970-01-06 | Texaco Inc | Preparation of a grease additive concentrate containing a water-soluble inorganic compound |
| US4052322A (en) * | 1976-06-24 | 1977-10-04 | Texaco Inc. | Corrosion-inhibited grease compositions |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE856773C (en) * | 1943-11-04 | 1952-11-24 | Hoechst Ag | lubricant |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2416281A (en) * | 1944-06-09 | 1947-02-25 | Socony Vacuum Oil Co Inc | Mineral oil composition |
| US2928789A (en) * | 1954-05-07 | 1960-03-15 | Monsanto Chemicals | Mineral oil compositions |
| CH357130A (en) * | 1957-07-11 | 1961-09-30 | Geigy Ag J R | Anti-rust agents |
| US2976243A (en) * | 1957-11-01 | 1961-03-21 | Exxon Research Engineering Co | Stable calcium acetate-mineral oil dispersion |
| US2989464A (en) * | 1959-12-23 | 1961-06-20 | Exxon Research Engineering Co | Stabilized suspensions of calcium acetate in oil |
| US3206399A (en) * | 1961-09-29 | 1965-09-14 | Socony Mobil Oil Co Inc | Diesel lubricating oil |
| NL280245A (en) * | 1961-06-30 |
-
1963
- 1963-02-19 US US259736A patent/US3259577A/en not_active Expired - Lifetime
-
1964
- 1964-02-17 GB GB6492/64A patent/GB1023710A/en not_active Expired
- 1964-02-18 NL NL6401443A patent/NL6401443A/xx unknown
- 1964-02-19 DE DES89599A patent/DE1258999B/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE856773C (en) * | 1943-11-04 | 1952-11-24 | Hoechst Ag | lubricant |
Also Published As
| Publication number | Publication date |
|---|---|
| US3259577A (en) | 1966-07-05 |
| GB1023710A (en) | 1966-03-23 |
| NL6401443A (en) | 1964-08-20 |
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