DE947419C - Metal working fluids made from natural or synthetic lubricating oils - Google Patents

Metal working fluids made from natural or synthetic lubricating oils

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Publication number
DE947419C
DE947419C DEC11173A DEC0011173A DE947419C DE 947419 C DE947419 C DE 947419C DE C11173 A DEC11173 A DE C11173A DE C0011173 A DEC0011173 A DE C0011173A DE 947419 C DE947419 C DE 947419C
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Germany
Prior art keywords
natural
oil
metal working
lubricating oils
percent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
DEC11173A
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German (de)
Inventor
Dr Wilhelm Dietrich
Dr Hans-Joachim Mertens
Dr Fritz Wetter
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Huels AG
Original Assignee
Chemische Werke Huels AG
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Application filed by Chemische Werke Huels AG filed Critical Chemische Werke Huels AG
Priority to DEC11173A priority Critical patent/DE947419C/en
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Publication of DE947419C publication Critical patent/DE947419C/en
Expired legal-status Critical Current

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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic compounds
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    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
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    • C10M2207/02Hydroxy compounds
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    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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    • C10M2219/06Thio-acids; Thiocyanates; Derivatives thereof
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    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
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    • C10N2040/20Metal working
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Description

Metallbearbeitungsflüssigkeiten aus natürlichen oder synthetischen Schmierölen Bekanntlich wird bei hohem Druck zwischen Werkzeug und Werkstück, wie er z. -B. an Werkzeugmaschinen mit großer Zerspanungs- oder Schneidleistung auftritt, der Ölfilm leicht zum Zerreißen gebracht. Dies führt zur Zerstörung. der, Oberfläche des Werkstückes und zu vorzeitiger Abnutzung des Werkzeuges.Metalworking fluids made from natural or synthetic Lubricating oils It is well known that when there is high pressure between the tool and the workpiece, such as he z. -B. occurs on machine tools with high machining or cutting performance, the oil film easily ruptured. This leads to destruction. the, surface of the workpiece and premature wear of the tool.

Die Erfindung bezieht sich auf Metallbearbeitungsflüssigkeiten aus natürlichen oder synthetischen Schmierölen, die auf Grund der besonderen Zusammensetzung ausgezeichnete Eigenschaften bezüglich der Verschleiß- und Abriebfestigkeit bei der spanabhebenden und spanlosen Verformung besitzen.The invention relates to metalworking fluids from natural or synthetic lubricating oils due to their special composition excellent properties in terms of wear and abrasion resistance the cutting and non-cutting deformation.

Es wurde gefunden, daß man aus Schmierölen natürlichen oder synthetischen Ursprungs durch Zusatz von, bezogen auf das 'Schmieröl, x bis 15 Gewichtsprozent einer schwefelhaltigen organischen Verbindung gemäß Patent 925 192, 929 38q., .g26 68o, 926 681 und 927 ßig oder 927 87,0, ferner von o,ooi bis 0,05 Gewichtsprozent eines öllöslichen sauren Esters der Säuren des Phosphors, außerdem von o,o2 bis 2 Gewichtsprozent eines Lösungsvermittlers gemäß Patent 929 384 sowie von o,= bis 2 Gewichtsprozent eines Korrosionsschutzmittels, zweckmäßig gemäß Patent 933 048, hervorragende Metallbearbeitungsflüssigkeiten erhält.It has been found that lubricating oils of natural or synthetic origin can be obtained by adding, based on the lubricating oil, x to 15 percent by weight of a sulfur-containing organic compound according to Patent 925 192, 929 38q., .G26 68o, 926 681 and 927 or 927 87.0, further from o, ooi to 0.05 weight percent of an oil-soluble acidic ester of the acids of phosphorus, also from o, o2 to 2 weight percent of a solubilizer according to patent 929 384 and from o, = to 2 weight percent of a corrosion inhibitor, expediently according to U.S. Patent 933,048, maintains excellent metalworking fluids.

Geeignete Schmieröle natürlichen oder synthetischen Ursprungs sind z. B. paraffinische, naphthenische Kohlenwasserstoffe, polymerisierte Olefine, alkylierte Aromaten, Ester aus Dicarbonsäuren und aliphatischen, mehrwertigen Alkoholen. Sie können ferner fette Öle mit Schmiermittelcharakter, z. B. Rizinusöl, Rüböl usw., in Mengen bis zu etwa zo Gewichtsprozent, enthalten.Suitable lubricating oils are of natural or synthetic origin z. B. paraffinic, naphthenic hydrocarbons, polymerized olefins, alkylated Aromatics, esters from dicarboxylic acids and aliphatic, polyhydric alcohols. she can also be fatty oils with lubricant character, z. B. castor oil, rapeseed oil, etc., in amounts up to about zo percent by weight.

Besonders geeignete schwefelhaltige organische Verbindungen sind organische Disulfide, wie sie durch Oxydation von Äthyl-, Propyl-, i-Propyl-, n-Butyl-, i-Butyl-, Amylxanthogenaten mit Persulfaten oder Natriumhypochlorit nach bekannten Verfahren erhalten werden können, ferner Polysulfide von Xanthogenaten, die aus den Alkalisalzen der" Di- und Trithiokohlensäure und Chlorschwefel gewonnen werden (vgl. Patent 925 r92).Particularly suitable sulfur-containing organic compounds are organic Disulfides, such as those produced by the oxidation of ethyl, propyl, i-propyl, n-butyl, i-butyl, Amyl xanthates with persulfates or sodium hypochlorite by known methods can be obtained, furthermore, polysulphides of xanthates, which are obtained from the alkali salts the "di- and trithiocarbonic acid and chlorosulfur can be obtained (cf. Patent 925 r92).

Ferner sind brauchbar: z. - Organische Schwefelverbindungen der allgemeinen Formel R- (S)n- R, in der ,R: Wasserstoff oder einen Alkyl-, Cycloalkyl-, Aryl-, Aralkyl- oder heterocyclischen Rest bedeutet, der gerädkettig oder verzweigt, gesättigt oder ungesättigt, substituiert oder nicht substituiert sein kann sowie gegebenenfalls noch Metalle, beispielsweise Zinn oder Zink, enthält, und n eine Zahl von z bis 5 oder höher bedeutet, z. B: Thiodiglykol, Thiodiglykolsäureester, Thiodipropionsäurebutylester, Didodecyldisulfid, Diamyltrisulfid, Di ß, ß'-oxäthyldisulfid, Diäthylöxäthyldisulfid, Di-(-thiopropionsäurebutylester), Diben-yldisulfid, Dihexylphenoldisulfid, Di-tert.-butylkresoldisulfid, Dibenzolthiazoldisulfid (Patent 929 384).Also useful are: z. - Organic sulfur compounds of the general Formula R- (S) n- R, in which, R: hydrogen or an alkyl, cycloalkyl, aryl, Aralkyl or heterocyclic radical means straight-chain or branched, saturated or unsaturated, substituted or unsubstituted and optionally still contains metals, for example tin or zinc, and n is a number from z to 5 or higher means e.g. B: thiodiglycol, thiodiglycolic acid ester, thiodipropionic acid butyl ester, Didodecyl disulfide, diamyl trisulfide, Di ß, ß'-oxäthyldisulfid, Diethylöxäthyldisulfid, Di - (- thiopropionic acid butyl ester), diben-yl disulfide, dihexylphenol disulfide, di-tert-butylcresol disulfide, Dibenzolthiazole disulfide (Patent 929,384).

z. Geschwefelte niedrigmolekulare Olefine, die durch aromatische Reste substituiert sind, wie Styrol, Stuben, Monophenylbutadien, Diphenylbutadien, Mononaphthylbutadien, Dinaphthylbutadien .(vgl. Patent 926 68o).z. Sulfurized low molecular weight olefins by aromatic residues are substituted, such as styrene, Stuben, monophenylbutadiene, diphenylbutadiene, mononaphthylbutadiene, Dinaphthylbutadiene (see patent 926 68o).

3. Geschwefelte Ester aus ungesättigten Carbonsäuren und ein- oder mehrwertigen Alkoholen; wie Acrylsäureäthylester, Crotonsäurebntylester, Crotonsäureallylester, die Äthyl-, Propyl-, Butyl-, Amyl-, Oktyl-, Glykol-, Propylenglykol-, Butylenglykol-, Äthyldiäthylenglykol- und Dicyclopentadienolester der Ölsäure, Linolsäure, Linolensäure (vgl. Patent 926 68i).3. Sulfurized esters of unsaturated carboxylic acids and one or polyhydric alcohols; such as ethyl acrylate, butyl crotonate, allyl crotonate, the ethyl, propyl, butyl, amyl, octyl, glycol, propylene glycol, butylene glycol, Ethyl diethylene glycol and dicyclopentadienol esters of oleic acid, linoleic acid, linolenic acid (see patent 926 68i).

4. Geschwefelte . ungesättigte Alkohole, z. B. Allylalkohol, Allylcarbinol, Oktendiol,. Dicyclopentadienol, a- und ß-Terpineol und andere (vgl. Patent 927 8=9), 5. Geschwefelte flüssige, nicht cyclische Olefine, wie Dipropylen, Tripopylen, Diisobutylen, Hexene, Äthylhexene und andere Olefine mit einem Siedebereich von etwa 7o bis 16o° (vgl. Patent 927 82o). , Die einzusetzende Menge der obengenannten schwefelhaltigen organischen Verbindungen ist abhängig vom Schwefelgehalt des Einzelmoleküls. Infolgedessen müssen - um den gewünschten Effekt zu erzielen - die unter z bis 5 genannten Verbindungen in. etwas größeren Mengen dem Grundöl zugesetzt werden als die Xanthogenverbindungen. -Als öllösliche saure Ester der- Säuren des Phosphors kommen in Frage saure Ester der Ortho-, Meta- und Pyrophosphorsäure, der phosphorigen und ünterphosphorigen Säure, wie die Mono- und Diphosphate des Butanols, Hexanols, Octanols, Laurylalkohols, Phenols, der Kresole des 4-Chlorbenzylalkohols bzw. die entsprechenden Mono- und Diester der phosphorigen und unterphosphorigen Säure. Auch Triester, soweit sie unter den jeweiligen Verhältnissen--sauer reagieren, z. B. die Umsetzungsprodukte der Phosphortrihalogenide mit 0xidogruppen enthaltenden Verbindungen, z. B. Äthylenoxyd, wie Tri-(chloräthanol-)phosphorigsäureester, Tri-(phenylchloräthanol)-ph6sphorigsäureester, haben sich als brauchbar erwiesen.4. Sulphurized. unsaturated alcohols, e.g. B. allyl alcohol, allyl carbinol, Octene diol ,. Dicyclopentadienol, α- and ß-terpineol and others (see patent 927 8 = 9), 5. Sulphurized liquid, non-cyclic olefins, such as dipropylene, tripylene, diisobutylene, Hexene, ethylhexene and other olefins with a boiling range of about 7o to 16o ° (see patent 927 82o). , The amount to be used of the above sulfur-containing organic compounds depends on the sulfur content of the single molecule. Consequently must - in order to achieve the desired effect - the compounds mentioned under z to 5 in. Somewhat larger amounts are added to the base oil than the xanthogen compounds. -As oil-soluble acidic esters der- acids of phosphorus come into question acidic esters ortho-, meta- and pyrophosphoric acid, phosphorous and hypophosphorous Acids, such as the mono- and diphosphates of butanol, hexanol, octanol, lauryl alcohol, Phenol, the cresols of 4-chlorobenzyl alcohol or the corresponding mono- and Diesters of phosphorous and hypophosphorous acids. Even Trieste, as far as they are under the respective conditions - react acidic, z. B. the conversion products of phosphorus trihalides with compounds containing oxido groups, e.g. B. ethylene oxide, such as tri- (chloroethanol) phosphorous acid ester, tri- (phenylchloroethanol) phosphorous acid ester, have proven to be useful.

Als Lösungsvermittler, die neben einem guten Löseverrriögen - für die Zusätze und einer guten Löslichkeit in den Schnv.erölen den Flammpunkt der Mischungen nicht herabsetzen und möglichst zusätzlich die korrosionsverhindernden Eigenschaften der in der folgenden Gruppe genannten Korrosionsschutzmittel noch verstärken sollen, kommen in Frage gesättigte, verzweigte oder unverzweigte aliphatische, substituierte oder unsubstituierte cycloaliphatische, aromatische, araliphatische Alkohole, die mit so viel Alkylenoxyd; z. B. Äthylen-, Propylen-, Butylenöxyd und/oder deren Gemischen,. umgesetzt wurden, daß viskose Produkte mit Molgewichten von etwa zooo und mehr entstehen. Geeignete Alkohole sind z. B. Äthyl-r, g-hexandiol, 2-Methyl-pentandiol-i, 4, 2-Äthylhexanolol, Laurylalkohol; von diesen wiederum sind mit Propylenoxyd umgesetzter Äthylhexyl- oder Laurylalkohol vom Molgewicht z2oo bzw. deren Gemische besonders geeignet wegen ihres ausgezeichneten Lösungsvermögens (vgl. Patent 927 8z9).As a solubilizer, who in addition to a good solution - for the additives and a good solubility in the snow oils, the flash point of the mixtures do not reduce and, if possible, additionally the corrosion-preventing properties the corrosion protection agents mentioned in the following group are intended to strengthen, Saturated, branched or unbranched aliphatic, substituted ones come into question or unsubstituted cycloaliphatic, aromatic, araliphatic alcohols, the with so much alkylene oxide; z. B. ethylene, propylene, butylene oxide and / or mixtures thereof. have been implemented that viscous products with molecular weights of about zooo and more arise. Suitable alcohols are e.g. B. Ethyl-r, g-hexanediol, 2-methyl-pentanediol-i, 4, 2-ethylhexanolol, Lauryl alcohol; of these, in turn, are ethylhexyl reacted with propylene oxide or lauryl alcohol with a molecular weight of 250 or mixtures thereof are particularly suitable because of their excellent solvent power (see patent 927 8z9).

Einem etwa möglichen Angriff .auf die zu bearbeitenden und zu schmierenden Metalloberflächen durch fremde, z. B. atmosphärische Einflüsse wird durch Zufügen. eines Korrosionsschutzmittels begegnet. Hierfür haben sich als besonders vorteilhaft solche hydroxylgruppenhaltige organische Verbindungen erwiesen, deren HydroxyIgrüppen an verschiedene, durch Äthersauerstoff verbundene Kohlenstoffatome gebunden- sind- und wobei eine der Hydroxylgruppen durch eine Fettsäure verestert ist, z. B. Diglykol-, Triglykol-, Propylenglykol-, Dipropylenglykol-, Tripropylenglykol-, Glycerin-, Diglycerin-, Sorbitol-, Sorbitan-, Hexäntriol , Pentaerythritmonooleat, -stearat usw. (vgl. Patent 933 048).A possible attack on those to be processed and lubricated Metal surfaces by foreign, z. B. atmospheric influences is by adding. encountered an anti-corrosion agent. This has proven to be particularly beneficial such hydroxyl-containing organic compounds have been found, their hydroxyl groups are bound to different carbon atoms connected by ether oxygen and wherein one of the hydroxyl groups is esterified by a fatty acid, e.g. B. diglycol, Triglycol, propylene glycol, dipropylene glycol, tripropylene glycol, glycerine, diglycerine, Sorbitol, sorbitan, hexanetriol, pentaerythritol monooleate, stearate, etc. (see patent 933 048).

In Abhängigkeit vom Verwendungszweck der Metallbeaxbeitungsflüssigkeiten schwanken die zuzusetzenden Mengen. an schwefelhaltigen organischen Verbindungen, sauren Estern der Säuren des Phosphors, Lösungsvermittlern und Korrosionsschutzmitteln innerhalb gewisser Grenzen. Der bevorzugte Bereich der zuzusetzenden Mengen liegt bei 3 bis 6 Gewichtsprozent, bezogen auf das Schmieröl, besonders bei den Xanthogenverbindungen enthaltenden Zusätzen. Im einzelnen kann, die Zusammensetzung etwa folgende sein: . Menge in Gewichtsprozent I Bevorzugter Bereich i. Schwefelhaltige organische Verbindungen ..... i bis 15 2 bis 5 2. Saure Ester der Säuren des Phosphors ...... o,ooi bis 0,o5 0,0025 bis 0,025 3. Lösungsvermittler .......................... o,2 bis 2,0 0,5 bis i,o 4. Korrosionsschutzmittel ..................... o,i bis 2,o o,5 bis i,o 5. Schmieröl................................. Rest Rest Es ist im allgemeinen zweckmäßig, die Zusätze zunächst miteinander zu mischen und dann erst dem Schmieröl zuzugeben. Doch kann man die Zusätze dem Schmieröl auch einzeln zugeben, wobei schwerlösliche Zusätze zweckmäßig in Verbindung mit dem Lösungsvermittler angewandt werden. Aber selbst dann, wenn die Zusätze sich ohne Hilfe von Lösungsvermittlern im Schmieröl lösen, bringt die Verwendung der Lösungsvermittler beträchtliche Vorteile, da sie es ermöglichen, daß die Zusätze sich bereits in der Kälte und ohne wesentlichen Aufwand an Arbeit und Energie im Grundöl klar und klarbleibend lösen.The amounts to be added vary depending on the intended use of the metal working fluids. of sulfur-containing organic compounds, acidic esters of the acids of phosphorus, solubilizers and anti-corrosion agents within certain limits. The preferred range of the amounts to be added is 3 to 6 percent by weight, based on the lubricating oil, particularly in the case of the additives containing xanthogen compounds. In detail, the composition can be about the following:. Amount in percent by weight I Preferred range i. Organic compounds containing sulfur ..... i to 15 2 to 5 2. Acid esters of the acids of phosphorus ...... o, ooi to 0, o5 0.0025 to 0.025 3. Solubilizer .......................... o, 2 to 2.0 0.5 to i, o 4. Corrosion protection agents ..................... o, i to 2, o o, 5 to i, o 5. Lube oil ................................. remainder remainder It is generally advisable to first mix the additives with one another and only then to add them to the lubricating oil. However, the additives can also be added individually to the lubricating oil, in which case additives that are difficult to dissolve are expediently used in conjunction with the solubilizer. But even if the additives dissolve in the lubricating oil without the aid of solubilizers, the use of the solubilizers brings considerable advantages, since they enable the additives to remain clear and clear in the base oil even in the cold and without significant expenditure of labor and energy to solve.

Außer den genannten Verbindungen können den Metallbearbeitungsflüssigkeiten von Fall zu Fall noch andere -Mittel, z. B. Antioxydantien, Mittel zur Erniedrigung des Stockpunktes, zum Verhindern von Schaumbildung oder zur Änderung der Viskosität, zugesetzt werden.Besides the above compounds the metalworking fluids can other from time to time - the means for. B. antioxidants, agents for lowering the pour point, for preventing foam formation or for changing the viscosity, may be added.

Die neuen Metallbearbeitungsflüssigkeiten zeichnen sich gegenüber den bekannten Mitteln durch ihre überlegenen Eigenschaften hinsichtlich der Korrosionsfestigkeit, der Belastbarkeit durch Druck und des Gleitens aus. Bei einem Vergleich dieser Metallbearbeitungsflüssigkeiten mit den gebräuchlichen Schneidölen ergab sich folgendes: Auf einer Prüfmaschine nach Krekeler-Honsberg wurden Zerspanbarkeitsuntersuchungen nach dem Einstichverfahren (vgl. Technische Mitteilung 46 [i953], S.45 bis 51) im Vergleich mit bekannten, im Handel befindlichen Schneidölen durchgeführt, wobei als Zerspanungswerkstoff ein Schnellautomatenwerkstahl sag S 2o« von io mm fö und als Werkzeug ein Einstechmeißel aus Schnellstahl Böhler SRE 214 verwandt wurde. Die Schneidölmenge wurde auf 2,31/min eingestellt. Die Schnittgeschwindigkeiten betrugen Va = ioo m/min Tdi = 30 m/min Vm = 65 m/min bei einem Vorschub von S = 0,014 mm/Umdr. und einer Einstechtiefe von C = 3,5 mm. Dabei ergab sich bei Verwendung einer Metallbearbeitungsflüssigkeit gemäß dem folgenden Beispiel i nach 80o Einstichen im Mittel aus j e drei Versuchen eine Verschleißmarkenbreitevon 0,o88 mm gegenüber o,129 mm bei Verwendung eines handelsüblichen Schneidöles bester Qualität. Bei der angegebenen Prüfmethode läßt sich die Zerspanungsleistung aus der Ankerstromaufnahme des Antriebsmotors bestimmen. Setzt man die Ankerstromaufnahme beim Trockenschnitt gleich ioo 0/0, so ergibt sich für die Metallbearbeitungsflüssigkeiten ein Wert von 61% gegenüber 78 % für ein handelsübliches Schneidöl.The new metalworking fluids are distinguished from the known agents by their superior properties in terms of corrosion resistance, resistance to pressure and sliding. A comparison of these metal working fluids with common cutting oils resulted in the following: On a testing machine according to Krekeler-Honsberg, machinability studies were carried out using the piercing method (cf. Technical Bulletin 46 [i953], pages 45 to 51) in comparison with known, commercially available cutting oils carried out using a high-speed automatic tool steel sag S 2o "of 10 mm fö as the cutting material and a grooving chisel made of high-speed steel Böhler SRE 214 as the tool. The amount of cutting oil was set to 2.31 / min. The cutting speeds were Va = 100 m / min Tdi = 30 m / min Vm = 65 m / min with a feed rate of S = 0.014 mm / rev. and a penetration depth of C = 3.5 mm. When using a metalworking fluid according to the following example i, after 80 ° punctures, an average of three tests each resulted in a wear mark width of 0.088 mm compared to 0.129 mm when using a commercial cutting oil of the best quality. With the specified test method, the cutting performance can be determined from the armature current consumption of the drive motor. If the armature current consumption during dry cutting is set equal to 100 0/0, the result for the metal working fluids is a value of 61% compared to 78% for a commercially available cutting oil.

Die neuen Metallbearbeitungsflüssigkeiten zeichnen sich ferner durch hervorragende Mischbarkeit und Verträglichkeit mit den üblichen Schmierstoffen, z. B. für die Lager der Werkzeugmaschinen aus.The new metalworking fluids are also characterized by excellent miscibility and compatibility with common lubricants, z. B. for the bearings of the machine tools.

In den nachfolgenden Beispielen werden besonders geeignete korrosionsfeste Metallbearbeitungsflüssigkeiten angeführt: Beispiel i 30/, Di-butylxanthogensäuredisulfid mit 1,290/, Schwefel, 0,0150/, Monoäthylhexylphosphorsäureester, 0,75 % Monoäthylhexyläther des Polypropylenglykols vom Molgewicht 750, 1% Gemisch aus Diglykolmonooleat und i, 2-Propylenglykolmonooleat, Rest Mineralöl von 2,5° E/5o°C.Particularly suitable corrosion-resistant metalworking fluids are listed in the following examples: Example i 30 /, di-butylxanthogenic acid disulfide with 1.290 /, sulfur, 0.0150 /, monoethylhexylphosphoric acid ester, 0.75% monoethylhexyl ether of polypropylene glycol with a molecular weight of 750, 1% mixture of diglycol monooleate and i , 2-propylene glycol monooleate, the remainder mineral oil at 2.5 ° E / 50 ° C.

Beispiel 2 5 % Di-äthylhexylxanthogensäuredisulfid mit 1,44% S, 0,015 % Tri(-chloräthanol)-phosphit, 0,5 0/0 Monoäthylhexyläther des Polyäthylenglykols vom Molgewicht 750, a,5 % Sorbitolmonooleat, Rest synthetisches Mineralöl auf Basis polymerisierter Olefine. Prüfungsergebnis: Verschleißmarkenbreite 0,o87 mm. Beispiel 3 80/, geschwefeltes Styrol laut Patent 82668o, 0,o8 % Monolaurylphosphat, 0,75)/, Monooktyläther des Polypropylenglykols vom Molgewicht 1050, 0,5 0/0 Diglycerinoleat, Rest Mineralöl von 2,5° E/5o°C. Prüfungsergebnis: Verschleißmarkenbreite o,ogo mm. Beispiel 4 io % geschwefelter Crotonsäurebutylester gemäß Patent 926 681, 0,o25 % Dibutylphosphat, 0,75 0/0 Monolauryläther des Polypropylenglykols vom Molgewicht 1250, 0,504 Sorbitolmonooleat Rest synthetisches Esteröl aus Dicarbonsäuren und aliphatischen mehrwertigen Alkoholen. Prüfungsergebnis: Verschleißmarkenbreite 0,o85 mm.Example 2 5% diethylhexylxanthogenic acid disulfide with 1.44% S, 0.015% tri (chloroethanol) phosphite, 0.5 0/0 monoethylhexyl ether of polyethylene glycol with a molecular weight of 750, a, 5% sorbitol monooleate, the remainder synthetic mineral oil based on polymerized olefins . Test result: wear mark width 0.087 mm. Example 3 80 /, sulfurized styrene according to patent 82668o, 0.08% monolauryl phosphate, 0.75) /, monooctyl ether of polypropylene glycol with a molecular weight of 1050, 0.5% diglycerol oleate, the remainder mineral oil at 2.5 ° E / 50 ° C . Test result: wear mark width o, ogo mm. EXAMPLE 4 10% sulphurized butyl crotonate according to Patent 926 681, 0.025% dibutyl phosphate, 0.75% monolauryl ether of polypropylene glycol with a molecular weight of 1250, 0.504 sorbitol monooleate, the remainder is synthetic ester oil from dicarboxylic acids and aliphatic polyhydric alcohols. Test result: wear mark width 0.085 mm.

Beispiel 5 7% geschwefeltes Triisobutylen (S-Geh. 32,4 )/o) nach Patent 927 82o, 0,0150/,) 4-Chlorbenzylmonophosphat, 1,50/, Monolauryläther des Polyäthylenpropylenglykols vom Molgewicht 750, 0,50/0 Diglycerinmonooleat, Rest Mineralöl 2,5° E/500 C. Prüfungsergebnis: Verschleißmarkenbreite o,088 mm.Example 5 7% sulfurized triisobutylene (S-Geh. 32.4) / o) according to patent 927 82o, 0.0150 /,) 4-chlorobenzyl monophosphate, 1.50 /, monolauryl ether of polyethylene propylene glycol with a molecular weight of 750, 0.50 / 0 Diglycerol monooleate, remainder mineral oil 2.5 ° E / 500 C. Test result: Wear mark width 0.088 mm.

Claims (1)

PATENTANSPRUCH: Metallbearbeitungsflüssigkeiten aus natürlichen oder synthetischen Schmierölen, enthaltend x bis 15 Gewichtsprozent, bezogen auf das Schmieröl, Einer schwefelhaltigen organischen Verbindung gemäß Patent 925 192, 97,9 384, 926 68o, 926 681, 927 81g oder 927 82o, ferner o,oo= bis 0,05 Gewichtsprozent eines öllöslichen sauren Esters der Säuren des Phosphors, o,o2 bis 2 Gewichtsprozent eines Lösungsvermittlers gemäß Patent 927 8rg und o,r bis 2 Gewichtsprozent eines Korrosionsschutzmittels, zweckmäßig gemäß Patent 933 o48. PATENT CLAIM: Metal working fluids made from natural or synthetic lubricating oils, containing x to 15 percent by weight, based on the lubricating oil, a sulfur-containing organic compound according to Patent 925 192, 97.9 384, 926 68o, 9 26 68 1 , 927 81g or 927 82o, further o , oo = to 0.05 percent by weight of an oil-soluble acidic ester of the acids of phosphorus, o, o2 to 2 percent by weight of a solubilizer according to patent 927 8rg and o, r to 2 percent by weight of an anti-corrosion agent, expediently according to patent 933 o48.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1076299B (en) * 1956-08-18 1960-02-25 Basf Ag Lubricating oils
DE1794240A1 (en) * 1968-06-05 1971-10-14 Quaker Chem Corp Mechanical processing of malleable metals
FR2602787A1 (en) * 1986-07-28 1988-02-19 Magyar Asvanyolaj Es Foeldgaz AUXILIARY PRODUCTS CONTAINING EXTREME-PRESSURE ADDITIVES FOR INDUSTRIAL MACHINING OF METALS

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1076299B (en) * 1956-08-18 1960-02-25 Basf Ag Lubricating oils
DE1794240A1 (en) * 1968-06-05 1971-10-14 Quaker Chem Corp Mechanical processing of malleable metals
FR2602787A1 (en) * 1986-07-28 1988-02-19 Magyar Asvanyolaj Es Foeldgaz AUXILIARY PRODUCTS CONTAINING EXTREME-PRESSURE ADDITIVES FOR INDUSTRIAL MACHINING OF METALS

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