DE1279269B - Lubricating oil - Google Patents
Lubricating oilInfo
- Publication number
- DE1279269B DE1279269B DER26750A DER0026750A DE1279269B DE 1279269 B DE1279269 B DE 1279269B DE R26750 A DER26750 A DE R26750A DE R0026750 A DER0026750 A DE R0026750A DE 1279269 B DE1279269 B DE 1279269B
- Authority
- DE
- Germany
- Prior art keywords
- methyl
- acid
- friction
- coefficient
- mineral oil
- 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
- 239000010687 lubricating oil Substances 0.000 title description 3
- 239000000314 lubricant Substances 0.000 claims description 13
- 239000002480 mineral oil Substances 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 9
- 235000010446 mineral oil Nutrition 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 5
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 claims description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 3
- 125000004494 ethyl ester group Chemical group 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims 1
- 235000014121 butter Nutrition 0.000 claims 1
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 8
- 239000003921 oil Substances 0.000 description 6
- 239000000654 additive Substances 0.000 description 5
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 5
- 235000021355 Stearic acid Nutrition 0.000 description 4
- LGXSXDYIDKQMNR-UHFFFAOYSA-N methyl 2,2,3,3,4-pentachlorobutanoate Chemical compound ClCC(C(C(=O)OC)(Cl)Cl)(Cl)Cl LGXSXDYIDKQMNR-UHFFFAOYSA-N 0.000 description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
- 229940099259 vaseline Drugs 0.000 description 4
- CBXATHHSNACSCY-UHFFFAOYSA-N 2,2,3,3,4-pentachlorobutanoic acid Chemical compound ClCC(C(C(=O)O)(Cl)Cl)(Cl)Cl CBXATHHSNACSCY-UHFFFAOYSA-N 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- QFPRKSPAULXGPL-UHFFFAOYSA-N 2,2,3,3-tetrachlorobutanoic acid Chemical compound CC(Cl)(Cl)C(Cl)(Cl)C(O)=O QFPRKSPAULXGPL-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- -1 ethyl pentachlorobutyrates Chemical class 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 230000010355 oscillation Effects 0.000 description 2
- RVBUZBPJAGZHSQ-UHFFFAOYSA-N 2-chlorobutanoic acid Chemical compound CCC(Cl)C(O)=O RVBUZBPJAGZHSQ-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000011436 cob Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
Classifications
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/044—Acids; Salts or esters thereof
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/042—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/044—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
- C10N2040/046—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/10—Running-in-oil ; Grinding
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/251—Alcohol-fuelled engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
- C10N2040/28—Rotary engines
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
BUNDESREPUBLIK DEUTSCHLAND DEUTSCHES S/jffiTWi· PATENTAMT Int. CL: FEDERAL REPUBLIC OF GERMANY GERMAN S / jffiTWi · PATENT OFFICE Int. CL:
ClOmClOm
AUSLEGESCHRIFTEDITORIAL
Deutsche Kl.: 23 c-1/01 German class: 23 c -1/01
Nummer: 1279 269Number: 1279 269
Aktenzeichen: P 12 79 269.7-43 (R 26750)File number: P 12 79 269.7-43 (R 26750)
Anmeldetag: 18. November 1959 .Filing date: November 18, 1959.
Auslegetag: 3. Oktober 1968Open date: October 3, 1968
Aus den französischen Patentschriften 1050 806, 1145 476 und 1193 094 und der deutschen Patentschrift 1214 350 sind Hochleistungsschmiermittel bekannt, welche aus Mineralöl mit einem Zusatz von Tetrachlorlaurinsäurebzw. Teträchlorbuttersäure öder auch von-Pentachlorbuttersäure, ■ gegebenenfalls gemeinsam mit einem Zusatz von Estern höherer Fettsäuren bestehen. Bei diesen Schmiermitteln hat es sich allerdings als nachteilig herausgestellt, daß sie bei normalen mittleren Belastungen, bei denen immerhin ein Ölfilm aus reinem Mineralöl beiseite geschoben werden würde und es deshalb des Zusatzes von fett+· sauren Produkten als Haftmittel bedarf, Ungleichmäßigkeiten in der Schmierwirkung auftreten, so daß diese Mittel nicht universell einsetzbar sind.From French patents 1050 806, 1145 476 and 1193 094 and the German patent specification 1214 350 high-performance lubricants are known, which are made from mineral oil with an addition of Tetrachlorauric acid or Tetrachlorobutyric acid or else also von-pentachlorobutyric acid, ■ optionally together with an addition of esters of higher fatty acids. With these lubricants it has However, it has been found to be disadvantageous that they under normal average loads, at least with which an oil film of pure mineral oil would be pushed aside and therefore the addition of fat + acidic products as an adhesive, unevenness in the lubricating effect occur, so that these funds are not universally applicable.
Aus der deutschen Patentschrift 1041624 ist es weiterhin bekannt, Ester langkettiger Fettsäuren zusammen mit Estern der Tetralaurinsäure Mineralölen zuzugeben. Doch auch solche Schmiermittel genügen noch nicht den heute erforderlichen Anforderungen.From the German patent specification 1041624 it is furthermore known, esters of long-chain fatty acids together with esters of tetralauric acid mineral oils admit. But even such lubricants do not yet meet the requirements required today.
Es wurde nun gefunden, daß man wesentlich verbesserte Schmiermittel erhält, wenn man einem Schmiermittel aus einem Mineralöl und 0,05 bis 2% Stearin-, Palmitin- oder Behensäure bzw. deren Ester mit 1 bis 3 Kohlenstoffatomen im Alkylrest zusätzlich noch 0,2 bis 3% des Methyl- oder Äthylesters der Pentachlorbuttersäure der FormelIt has now been found that significant improvements have been made Lubricant is obtained by using a lubricant made from a mineral oil and 0.05 to 2% Stearic, palmitic or behenic acid or their esters with 1 to 3 carbon atoms in the alkyl radical still 0.2 to 3% of the methyl or ethyl ester of pentachlorobutyric acid of the formula
CCl3 — CHCl — CHCl — COOHCCl 3 - CHCl - CHCl - COOH
zusetzt. ,clogs. ,
Die benötigten Methyl- oder Äthylpentachlorbutyrate werden in bekannter Weise durch unmittelbare Veresterung der Pentachlorbuttersäure mit an SchmierölThe required methyl or ethyl pentachlorobutyrates are in a known manner by immediate Esterification of pentachlorobutyric acid with an lubricating oil
Anmelder:Applicant:
Regie Nationale des Usines Renault,
Billancourt, Seme (Frankreich)Directed by Nationale des Usines Renault,
Billancourt, Seme (France)
Vertreter:Representative:
DipL-Ing. C.H.Huss, Patentanwalt,'DipL-Ing. C.H. Huss, patent attorney, '
8100 Gapnisch-Partenkirchen^Rathausstr. 148100 Gapnisch-Partenkirchen ^ Rathausstr. 14th
Beanspruchte Priorität:Claimed priority:
Frankreich vom 21. November 1958 (779 796)France of November 21, 1958 (779 796)
Ghlorgas gesättigtem Methyl- oder Äthylalkohol erhalten. Ghlorgas saturated methyl or ethyl alcohol obtained.
ao Das erfindungsgemäße Schmiermittel gewährleistet bei Höchstdrücken das Gleiten ohne Festfressen wie die Schmiermittel nach dem Stand der Technik, und es hat darüber hinaus im Schmierbereich einen geringeren Reibungskoeffizienten, der bei mittleren Drücken in einem weiten Temperaturbereich stabil bleibt und auch gegenüber dem Schmiermittei gemäß der deutschen Patentschrift 1041624 seine stabile Schmierfähigkeit erst bei erheblich höheren Temperaturen verliert. Außerdem bewirkt das erfindungsgemäße Schmiermittel gegenüber Stahl eine ungewöhnlich geringe Korrosionswirkung. ; Die Tabelle I zeigt Ergebnisse, die mit der Vorrichtung von Bberl'age bei Drücken zwischen 250 und kg/mm2 ermittelt wurden.ao The lubricant according to the invention ensures sliding at maximum pressures without seizing like the lubricants according to the prior art, and it also has a lower coefficient of friction in the lubricating area, which remains stable over a wide temperature range at medium pressures and also compared to the lubricant according to the German patent 1041624 loses its stable lubricity only at significantly higher temperatures. In addition, the lubricant according to the invention has an unusually low corrosive effect on steel. ; Table I shows results which were determined with the device from Bberl'age at pressures between 250 and kg / mm 2 .
+ l°/oPenta- ·..-
chlorbutyrat
* 0,5 °/o Stearin
säuremineral oil
+ l ° / oPenta- ..-
chlorobutyrate
* 0.5 per cent stearin
acid
Mineralöl
+ lo/oMethyl-
^teärat■ / -
mineral oil
+ lo / o methyl
^ teärat
Mineralöl
+0,5 %> Stearin
säure-, }, · - / ■ -
mineral oil
+ 0.5%> stearin
acid
Mineralöl
rein . "■ - 1 V- 1 I 1 i
mineral oil
pure
.+ l%Penta-\,
chlorbutyrat -r*
+ 1%Methyl-,
stearatmineral oil
. + l% penta \,
chlorobutyrate - r *
+ 1% methyl,
stearate
11080
110
9570
95
-- 9060
- 90
8060
80
kg/mm2 .;, .Highest pressure without seizing,
kg / mm 2 .;,.
12080
120
Festfressen, kg/mm2 Lowest pressure when suddenly
Seizure, kg / mm 2
Der Zusatz von Methylpentachlorbutyrat zu Mineralölen in Verbindung mit Stearinsäure oder dem Methylester der Stearinsäure verbessert wesentlich die Widerstandsfähigkeit gegen Festfressen bei ungewöhnlich hohen Drücken.The addition of methyl pentachlorobutyrate to mineral oils in conjunction with stearic acid or the Methyl ester of stearic acid significantly improves the resistance to seizing when abnormal high pressures.
809 619/536809 619/536
In der Tabellen sind die Reibungskoeffizienten und deren mittlere Abweichungen, gemessen mittels der Vorrichtung von Her schell bei verschiedenen Temperaturen, angegeben.In the tables are the coefficients of friction and their mean deviations, measured by means of the Her schell device, at various Temperatures.
1. Reines VaselinöT 98%1.Pure vaseline oil 98%
Methylpentachlorbutyrat 1%Methyl pentachlorobutyrate 1%
Methylstearat ... 1%Methyl stearate ... 1%
2. Vaselinöl 98,5°/o2. Vaseline oil 98,5 ° / o
Methylpentachlorbutyrat 1%Methyl pentachlorobutyrate 1%
Stearinsäure 0,5%Stearic acid 0.5%
3. Reines Vaselinöl3. Pure petroleum jelly
4. Reines Vaselinöl mit 5%igem handelsüblichem Zusatz für Hochdrucköl· 4. Pure vaseline oil with 5% commercial additive for high pressure oil
TabeUeHTabeUeH
mit sehr starken Abweichungenunstable area
with very strong deviations
Im Falle der Mischung 1 bleibt der Reibungskoeffizient extrem schwach, und er bleibt sehr as schwach im Falle der Mischung 2, selbst bei Temperaturen von 115° C,' ganz im Gegensatz zu den Mischungen 3 und 4, die einen hohen Reibungskoeffizienten und eine starke Streuung bei Normaltemperatur zeigen.In the case of mixture 1, the coefficient of friction remains extremely weak, and it remains very weak in the case of Mix 2, even at temperatures of 115 ° C, 'in complete contrast to mixtures 3 and 4, which have a high coefficient of friction and show a strong scatter at normal temperature.
Besonders bemerkenswert ist es, daß in der erfindungsgemäßen Mischung 1 auch bei den Temperaturen 100 und 115° C noch keine erheblichen Schwankungen in der Anzeige der Reibungskoeffizienten auftreten. Dies steht im Gegensatz gegenüber der deutschen Patentschrift 1041624. Aus Fig. 7 dieser Patentschrift ergibt sich deutlich, daß bereits bei 100° C eine Aufspaltung der für die Reibungskoeffizienten gefundenen Werte in zwei Kurvenäste stattfindet. Bei einer Temperatur von 115° C ist also nicht nur der Reibungskoeffizient von 0,120 bei Verwendung von TetracMorlaurinsäuremethylester (1%) mit Stearinsäur emethylester.(l%) auf 0,107 bei Verwendung von PentacHorbuttersäuremethylester (1 %) mit Stearinsäuremethylester (1%) herabgesetzt, sondem die Temperaturgrenze von 100° C, bei der die Instabilität des Reibungskoeffizienten bei dem erstgenannten Schmieröl beginnt, ist bei dem erfindungsgemäßen Schmiermittel um mindestens 15° C heraufgesetzt. Die erfindungsgemäßen Schmiermittel eignen sich vorzugsweise für die Schmierung von Explosionsmotoren während der Einlaufzeit und für die dauernde Schmierung von Transmissionen, Getriebekasten, für konische Kupplungen.It is particularly noteworthy that in the invention Mixture 1 still shows no significant fluctuations in the display of the coefficient of friction even at temperatures of 100 and 115 ° C appear. This is in contrast to German patent specification 1041624. From FIG. 7 This patent specification clearly shows that even at 100 ° C. there is a split in the coefficients of friction found values takes place in two branches of the curve. So at a temperature of 115 ° C not only the coefficient of friction of 0.120 when using TetracMorlauric acid methyl ester (1%) with methyl stearate (1%) to 0.107 when using methyl pentacate (1%) with stearic acid methyl ester (1%) reduced, special the temperature limit of 100 ° C at which the Instability of the coefficient of friction begins with the first-mentioned lubricating oil is in the case of the invention Lubricant increased by at least 15 ° C. The lubricants according to the invention are suitable preferably for the lubrication of explosion engines during the running-in period and for the permanent lubrication of transmissions, gear boxes, for conical couplings.
Tabelle ΙΠTable ΙΠ
Vergleichswerte der SchwankungsbreiteComparative values of the fluctuation range
der Reibungskoeffizienten im Herschell-Gerätthe coefficient of friction in the Herschell device
bei 15 kg/mm2 Durchschnittsberührungsdrücken.at 15 kg / mm 2 average contact pressures.
Geprüft wurde Vaselinöl mit jeweils 1 GewichtsprozentVaseline oil was tested with 1 percent by weight each
der angegebenen Zusatzmittel. Dabei bedeutet St. = Stearinsäuremethylester.of the specified additives. St. = methyl stearate.
In allen Fällen gerät der Kugelwagen in starke Oszillation und zeigt auch hierdurch die ungenügende Schmierfähigkeit in diesem Belastungsbereich an.In all cases the ball runner block gets into strong oscillation and this also shows the insufficient oscillation Lubricity in this load range.
Vergleichswerte der-Reibungskoeffizienten im Herschell-Gerät für Schmiermittel gemäß deutschem Patent 1041624 bei 15 kg/mm2 Berührungsdrücken in Abhängigkeit zur Temperatur für folgende Zusätze:Comparative values of the coefficient of friction in the Herschell device for lubricants according to German patent 1041624 at 15 kg / mm 2 contact pressures depending on the temperature for the following additives:
• \ .. A = 1% Tetrachlorlaurinsäuremethylester + 1% Methylstearat B = 1% Pentachlorbuttersäuremethylester + 1% Methylstearat• \ .. A = 1% methyl tetrachloroate + 1% methyl stearate B = 1% methyl pentachlorobutyrate + 1% methyl stearate
50°CRubs
50 ° C
75° Cing coefficient
75 ° C
100° Csn at
100 ° C
0,1300.120
0.130
0,1140.120
0.114
0,1100.115
0.110
0,1000.110 *
0.100
0,1071.120 **
0.107
Der mit *' gekennzeichnete Wert" steht am Beginn einer Instabilität.The value marked with * 'is at the beginning of an instability.
Der mit ** gekennzeichnete Wert gibt den Höchstwert einer starken Instabilität schwankender ReibungSrkoeffizienten. The value marked with ** indicates the maximum value of a strong instability of fluctuating friction coefficients.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR779796A FR1215903A (en) | 1958-11-21 | 1958-11-21 | Lubricants for loaded mechanisms |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1279269B true DE1279269B (en) | 1968-10-03 |
Family
ID=8708531
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DER26750A Pending DE1279269B (en) | 1958-11-21 | 1959-11-18 | Lubricating oil |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3117932A (en) |
| DE (1) | DE1279269B (en) |
| FR (1) | FR1215903A (en) |
| GB (1) | GB922486A (en) |
| NL (2) | NL244855A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0004957A3 (en) * | 1978-04-26 | 1980-04-16 | Ciba-Geigy Ag | Compositions and use of chlorinated derivatives of butyric acid as additives for lubricants |
| US6028038A (en) * | 1997-02-14 | 2000-02-22 | Charles L. Stewart | Halogenated extreme pressure lubricant and metal conditioner |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1098408A (en) * | 1954-04-13 | 1955-07-26 | Renault | Lubricants for loaded mechanisms |
| GB784896A (en) * | 1955-01-11 | 1957-10-16 | Algemene Kunstzijde Unie Nv | Improved method and device for the manufacture of artificial threads and like products |
| DE1214350B (en) * | 1958-03-06 | 1966-04-14 | Renault | High performance lubricant |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA54031A (en) * | 1896-10-06 | 1896-11-10 | William Squires | Bicycle gearing |
| US2210140A (en) * | 1931-11-06 | 1940-08-06 | Colbeth Ivor Milton | Lubricant and process of producing it |
| FR1050806A (en) * | 1952-02-13 | 1954-01-11 | Renault | Lubricants for heavily loaded components |
| US2877182A (en) * | 1952-09-08 | 1959-03-10 | Dow Corning | Organosilicon lubricants |
-
0
- NL NL121572D patent/NL121572C/xx active
- NL NL244855D patent/NL244855A/xx unknown
-
1958
- 1958-11-21 FR FR779796A patent/FR1215903A/en not_active Expired
-
1959
- 1959-10-27 US US848892A patent/US3117932A/en not_active Expired - Lifetime
- 1959-10-28 GB GB36669/59A patent/GB922486A/en not_active Expired
- 1959-11-18 DE DER26750A patent/DE1279269B/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1098408A (en) * | 1954-04-13 | 1955-07-26 | Renault | Lubricants for loaded mechanisms |
| GB784896A (en) * | 1955-01-11 | 1957-10-16 | Algemene Kunstzijde Unie Nv | Improved method and device for the manufacture of artificial threads and like products |
| DE1214350B (en) * | 1958-03-06 | 1966-04-14 | Renault | High performance lubricant |
Also Published As
| Publication number | Publication date |
|---|---|
| NL121572C (en) | |
| GB922486A (en) | 1963-04-03 |
| FR1215903A (en) | 1960-04-21 |
| NL244855A (en) | |
| US3117932A (en) | 1964-01-14 |
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