DE1071869B - Scbmierölzusatlz - Google Patents
ScbmierölzusatlzInfo
- Publication number
- DE1071869B DE1071869B DENDAT1071869D DE1071869DA DE1071869B DE 1071869 B DE1071869 B DE 1071869B DE NDAT1071869 D DENDAT1071869 D DE NDAT1071869D DE 1071869D A DE1071869D A DE 1071869DA DE 1071869 B DE1071869 B DE 1071869B
- Authority
- DE
- Germany
- Prior art keywords
- lubricating oil
- oil additive
- oil
- percent
- 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.)
- Pending
Links
- 239000000654 additive Substances 0.000 title claims description 9
- 230000000996 additive effect Effects 0.000 title claims description 6
- 239000010687 lubricating oil Substances 0.000 title claims description 4
- -1 alkoxy ester Chemical class 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 3
- 230000001476 alcoholic effect Effects 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 150000002148 esters Chemical class 0.000 description 6
- 239000010802 sludge Substances 0.000 description 5
- 150000001991 dicarboxylic acids Chemical class 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- QMPKJVBRCQVFLL-UHFFFAOYSA-N 1,1,2-triphenylethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)CC1=CC=CC=C1 QMPKJVBRCQVFLL-UHFFFAOYSA-N 0.000 description 1
- GIMDPFBLSKQRNP-UHFFFAOYSA-N 1,1-diphenylethanol Chemical compound C=1C=CC=CC=1C(O)(C)C1=CC=CC=C1 GIMDPFBLSKQRNP-UHFFFAOYSA-N 0.000 description 1
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- MUVQKFGNPGZBII-UHFFFAOYSA-N 1-anthrol Chemical class C1=CC=C2C=C3C(O)=CC=CC3=CC2=C1 MUVQKFGNPGZBII-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229960004217 benzyl alcohol Drugs 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- KTHXBEHDVMTNOH-UHFFFAOYSA-N cyclobutanol Chemical compound OC1CCC1 KTHXBEHDVMTNOH-UHFFFAOYSA-N 0.000 description 1
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- QILSFLSDHQAZET-UHFFFAOYSA-N diphenylmethanol Chemical compound C=1C=CC=CC=1C(O)C1=CC=CC=C1 QILSFLSDHQAZET-UHFFFAOYSA-N 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- YFONKFDEZLYQDH-BOURZNODSA-N indaziflam Chemical compound CC(F)C1=NC(N)=NC(N[C@H]2C3=CC(C)=CC=C3C[C@@H]2C)=N1 YFONKFDEZLYQDH-BOURZNODSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- LZTRCELOJRDYMQ-UHFFFAOYSA-N triphenylmethanol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)C1=CC=CC=C1 LZTRCELOJRDYMQ-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene 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
- C10M145/00—Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
- C10M145/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/10—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
- C10M145/16—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate polycarboxylic
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F22/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F22/10—Esters
- C08F22/12—Esters of phenols or saturated alcohols
- C08F22/20—Esters containing oxygen in addition to the carboxy oxygen
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/12—Esters of phenols or saturated alcohols
- C08F222/20—Esters containing oxygen in addition to the carboxy oxygen
- C08F222/205—Esters containing oxygen in addition to the carboxy oxygen the ester chains containing seven or more carbon atoms
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L35/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L35/02—Homopolymers or copolymers of esters
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
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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
- C10M2207/30—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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- 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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- 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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- 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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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/086—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type polycarboxylic, e.g. maleic acid
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
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- C10M2213/00—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
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- C10M2213/00—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2213/04—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions obtained from monomers containing carbon, hydrogen, halogen and oxygen
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- C10M2213/00—Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2213/06—Perfluoro polymers
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- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/026—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrile group
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- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- 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
- C10M2217/042—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds between the nitrogen-containing monomer and an aldehyde or ketone
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- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/043—Mannich bases
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- C10M2221/02—Macromolecular compounds obtained by reactions of monomers involving only carbon-to-carbon unsaturated bonds
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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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- 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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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Lubricants (AREA)
Description
DEUTSCHES
PATENTAMT
kl. 23 c 1/01
INTEBNAT. Kt. C 10 Hl
C 1OM I6S/0OA 28
E16462 IVc/23c
ANMELDETAG: 20. SEPTEMBER 1958
BEKANNTMACHUNG
DER ANMELDUNG
OND AUSGABE DER
AÜSLEGESCHRIFT.· 24. DEZEMBER 1959
DER ANMELDUNG
OND AUSGABE DER
AÜSLEGESCHRIFT.· 24. DEZEMBER 1959
Gegenstand des Patentes 1 037 630 ist die Verwendung von 0,01 bis 20 Gewichtsprozent eines öllöslichen
Mischpolymeren eines Alkoxymischesters, der von einer mit einem aliphatischen Alkohol teilweise
veresterten, mit einem Alkylenoxyd umgesetzten ungesättigten Dicarbonsäure abstammt, mit einem ungesättigten
Ester als Schmierölzusatz.
Die Zusatzstoffe gemäß Hauptpatent sind gute Detergentien, verursachen keine störenden Abscheidungen
in Verbrennungsmotoren und haben einen erhöhten Viskositätsindex und einen gesenkten Fließpunkt.
Als Zusatzstoffe gemäß vorliegender Erfindung werden 0,01 bis 20 Gewichtsprozent eines öllöslichen
Mischpolymeren aus einem ungesättigten Ester und einem solchen Alkoxymischester verwendet, dessen
zur Teilveresterung der ungesättigten Dicarbonsäure eingesetzte alkoholische Komponente ein cyclischer
oder aromatischer Alkohol oder ein Phenol ist.
Als aromatische Alkohole sind Phenylmethanol oder Phenyläthanol, ferner sek. aromatische Alkohole wie
Diphenylmethanol oder Diphenyläthanol, weiterhin tert. aromatische Alkohole wie Triphenylmethanol oder
Triphenyläthanol zu nennen.
Cyclische Alkohole sind z. B. Cyclobutanol und Cyclohexandiol. Geeignete Phenole sind unter anderem
Monophenole, Polyphenole, Naphthole und Anthranole oder substituierte Phenole, namentlich Monophenole,
die durch eine C8 bis C24-Alkylkette substituiert sind.
Bevorzugt wird z. B. Dodecylphenol, der etwa durch Substitution eines Phenols mit einer durch Propylenpolymerisation
erhaltenen Alkylkette gewonnen werden kann.
Die bevorzugten Dicarbonsäuren und Alkylenoxyde entsprechen denen des Patents 1 037 630; zu nennen
sind hier ebenfalls vornehmlich Fumarsäure, Maleinsäure als Dicarbonsäuren und Äthylenoxyd oder Propylenoxyd
als Alkylenoxyde.
Die Zusatzstoffe sind Mischpolymere der Alkoxymischester mit ungesättigten Estern z. B. Vinylacetat,
ferner Estern eines oder mehrerer C8- bis C12-Alkohole
wie Octylalkohol und einer a-/?-ungesättigten Monocarbonsäure,
insbesondere die Acrylate und Methacrylate.
1 Mol Maleinsäureanhydrid wird mit 1 Mol Dodecylphenol in Gegenwart von 1 % p-Toluolsulfonsäure
als Katalysator teilverestert; das Reaktionswasser wird mit Xylol entfernt.
Dieser Monoester wird mit Äthylenoxyd bei 140° C in Gegenwart von Spuren eines BF3-Äther-Komplexes
in 8 Stunden kondensiert. Der äthoxylierte Monoester Schmierölzusatz
Zusatz zum Patent 1 037 630
Anmelder:
Esso Standard
Societe Anonyme Francaise,
Paris
Paris
Vertreter: E. Maemecke, Berlin-Lichterfelde West,
und Dr. W. Kühl, Hamburg 36, Esplanade 36 a,
Patentanwälte
Beanspruchte Priorität:
Frankreich vom 24. September 1957
Frankreich vom 24. September 1957
Charles Rihouet, Paris,
und Edouard Thomas, Vincennes, Seine (Frankreich),
sind als Erfinder genannt worden
sind als Erfinder genannt worden
wird dann mit 25 Gewichtsprozent Vinylacetat in Gegenwart von Benzoylperoxyd als Katalysator
6 Stunden bei 70° C mischpolymerisiert.
Der Alkoxymischester wird in einem paraffinbasischen Mineralöl einer Viskosität von 35 cst bei
37,8° C und mit einem Viskositätsindex von 112 in verschiedenen Mengen gelöst: Die eine Lösung —
Lösung A — enthält 1 Gewichtsprozent, die andere Lösung — Lösung B — 5 Gewichtsprozent Zusatzstoff.
Die Detergenswirkung dieser Lösungen wird in der Weise untersucht, daß 10 g Trockenschlamm eines gebrauchten
Motoröls in 90 g des Testöls bei 93,3° C suspendiert werden und die Suspension 24 Stunden
bei dieser Temperatur stehengelassen wird. Danach werden die oberen 25 ecm des Gemisches in ein Zentrifugenrohr
abgegossen und mit Hexan auf 100 ecm aufgefüllt. Dieses Gemisch wird dann zentrifugiert
und der Schlamm gesammelt, um die Fähigkeit der ölvermischung zur Schlammsuspendierung auszuwerten.
Die Wirksamkeit des Zusatzstoffes wird durch das Verhältnis des Volumens des suspendierten
909 690/528
Schlamms (VI) zum Volumen des ursprünglich eingeführten Schlamms (VO) gemessen.
| Wirksamkeit — |
VI
VO |
•100 | Wirksamkeit |
| Testöl | 0 | ||
| Grundöl | 30 45 |
||
| Vermischung A | |||
| Vermischung B | |||
Claims (2)
1. Verwendung von 0,01 bis 20 Gewichtsprozent eines öllöslichen Mischpolymeren als Schmierölzusatz
nach Patent 1037 630, dadurch gekennzeichnet,
daß die alkoholische Komponente des Alkoxymischesters ein aromatischer oder cyclischer
Alkohol oder ein Phenol ist.
2. Verwendung von Mischpolymeren nach Anspruch 1, dadurch gekennzeichnet, daß die alkoholische
Komponente der Alkoxymischester ein Alkylphenol, insbesondere Dodecy!phenol, ist.
® 909 690/528 12.?»
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1123354T | 1955-03-09 | ||
| FR72338T | 1958-03-03 | ||
| FR759580A FR73165E (fr) | 1955-03-09 | 1958-03-03 | Produits d'addition pour huiles lubrifiantes et leur procédé de fabrication |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1071869B true DE1071869B (de) | 1959-12-24 |
Family
ID=27245087
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT1071869D Pending DE1071869B (de) | 1955-03-09 | Scbmierölzusatlz | |
| DEE12062A Pending DE1037630B (de) | 1955-03-09 | 1956-03-08 | Schmieroelzusatz |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEE12062A Pending DE1037630B (de) | 1955-03-09 | 1956-03-08 | Schmieroelzusatz |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3010906A (de) |
| DE (2) | DE1037630B (de) |
| FR (3) | FR1123354A (de) |
| GB (3) | GB788129A (de) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1226563A (fr) * | 1959-02-20 | 1960-07-13 | Exxon Standard Sa | Graisses améliorées |
| US3223636A (en) * | 1961-05-23 | 1965-12-14 | Exxon Research Engineering Co | Lead corrosion inhibitor |
| NL109759C (de) * | 1961-12-29 | |||
| US3215632A (en) * | 1962-06-22 | 1965-11-02 | Shell Oil Co | Lubricating compositions |
| US3285887A (en) * | 1962-07-30 | 1966-11-15 | Chevron Res | Microgel polymers |
| US3254058A (en) * | 1963-03-06 | 1966-05-31 | Exxon Research Engineering Co | Gel and sediment prevention in polymeric additives for hydrocarbon oils |
| US3459733A (en) * | 1964-10-15 | 1969-08-05 | Mobil Oil Corp | Monomeric polyesters of polyhydroxy compounds and process for preparing same |
| US3729296A (en) * | 1966-10-14 | 1973-04-24 | Exxon Research Engineering Co | Polymeric wax crystal modifiers for high wax content petroleum oils |
| US3933761A (en) * | 1971-03-17 | 1976-01-20 | The Lubrizol Corporation | Nitrogen-containing ester and lubricant containing the same |
| DE3136931A1 (de) * | 1981-09-17 | 1983-04-07 | Akzo Gmbh, 5600 Wuppertal | Copolymere aus (alpha)-(beta)-ungesaettigten dicarbonsaeureestern, verfahren zu deren herstellung sowie deren verwendung als gleitmittel fuer die kunststoffverarbeitung |
| CN113527568B (zh) * | 2021-08-04 | 2022-05-31 | 刚和石油(营口)有限公司 | 一种改性甲基丙烯酸酯聚合物及其润滑组成物 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2703811A (en) * | 1955-03-08 | Dibasic acid esters of glycols | ||
| BE380814A (de) * | 1930-06-26 | |||
| US2255313A (en) * | 1937-08-06 | 1941-09-09 | Ellis Foster Co | Ethylenic-alpha-beta synthetic resins and process of making same |
| US2418688A (en) * | 1942-08-11 | 1947-04-08 | Nat Dairy Prod Corp | Method of making an elastic polymer by milling and heating glycol with a copolymer of an alkyl acrylate and maleic anhydride |
| US2384595A (en) * | 1943-05-31 | 1945-09-11 | Petrolite Corp | Lubricating oil |
| DE842340C (de) * | 1944-04-09 | 1952-06-26 | Basf Ag | Verfahren zur Herstellung von Polycarbonsaeureabkoemmlingen |
| US2533376A (en) * | 1946-06-14 | 1950-12-12 | Libbey Owens Ford Glass Co | Copolymerization of maleic anhydride and allyl esters of long chain monocarboxylic acids |
| BE478881A (de) * | 1947-02-14 | |||
| US2616851A (en) * | 1947-04-29 | 1952-11-04 | Socony Vacuum Oil Co Inc | Mineral oil composition containing esters of product obtained by reaction between maleic anhydride and vinyl acetate |
| US2570788A (en) * | 1948-02-17 | 1951-10-09 | Socony Vacuum Oil Co Inc | Synthetic lubricants |
| US2607761A (en) * | 1948-04-10 | 1952-08-19 | Ind Res Inst Of The University | Reaction products of alkylene oxides and synthetic polymeric carboxylic acids |
| US2615845A (en) * | 1948-08-02 | 1952-10-28 | Standard Oil Dev Co | Lubricating oil additives |
| US2704277A (en) * | 1949-02-18 | 1955-03-15 | Socony Vacuum Oil Co Inc | Mineral oil compositions containing esterified copolymers of alpha,-beta-unsaturated polybasic acids with allyl and vinyl ethers |
| US2559510A (en) * | 1949-04-21 | 1951-07-03 | Standard Oil Dev Co | Synthetic lubricants |
| GB663702A (en) * | 1949-09-10 | 1951-12-27 | Standard Oil Dev Co | Improvements in or relating to copolymers and to lubricant compositions containing them |
| US2721878A (en) * | 1951-08-18 | 1955-10-25 | Exxon Research Engineering Co | Strong acid as a polymerization modifier in the production of liquid polymers |
| US2721877A (en) * | 1951-08-22 | 1955-10-25 | Exxon Research Engineering Co | Lubricating oil additives and a process for their preparation |
| US2824840A (en) * | 1953-04-01 | 1958-02-25 | Exxon Research Engineering Co | Lubricating oil composition |
| US2993032A (en) * | 1956-02-03 | 1961-07-18 | California Research Corp | Detergent copolymers |
| NL238305A (de) * | 1958-04-21 |
-
0
- DE DENDAT1071869D patent/DE1071869B/de active Pending
-
1955
- 1955-03-09 FR FR1123354D patent/FR1123354A/fr not_active Expired
- 1955-12-14 GB GB35913/55A patent/GB788129A/en not_active Expired
-
1956
- 1956-01-26 US US561676A patent/US3010906A/en not_active Expired - Lifetime
- 1956-03-08 DE DEE12062A patent/DE1037630B/de active Pending
-
1957
- 1957-09-24 FR FR72338D patent/FR72338E/fr not_active Expired
-
1958
- 1958-03-03 FR FR759580A patent/FR73165E/fr not_active Expired
- 1958-08-28 GB GB27626/58A patent/GB832057A/en not_active Expired
- 1958-10-07 GB GB31954/58A patent/GB833977A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1123354A (fr) | 1956-09-20 |
| US3010906A (en) | 1961-11-28 |
| FR73165E (fr) | 1960-09-23 |
| GB832057A (en) | 1960-04-06 |
| FR72338E (fr) | 1960-04-06 |
| DE1037630B (de) | 1958-08-28 |
| GB833977A (en) | 1960-05-04 |
| GB788129A (en) | 1957-12-23 |
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