DE1594365A1 - Hydraulic fluid - Google Patents
Hydraulic fluidInfo
- Publication number
- DE1594365A1 DE1594365A1 DE19671594365 DE1594365A DE1594365A1 DE 1594365 A1 DE1594365 A1 DE 1594365A1 DE 19671594365 DE19671594365 DE 19671594365 DE 1594365 A DE1594365 A DE 1594365A DE 1594365 A1 DE1594365 A1 DE 1594365A1
- Authority
- DE
- Germany
- Prior art keywords
- viscosity
- liquid
- hydraulic fluid
- denormalized
- hydraulic
- 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
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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
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
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- 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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- 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
- C10M2203/102—Aliphatic fractions
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- 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
- C10M2203/104—Aromatic fractions
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/106—Naphthenic fractions
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- 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
- C10M2203/108—Residual fractions, e.g. bright stocks
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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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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/024—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings having at least two phenol groups but no condensed ring
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/124—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms containing hydroxy groups; Ethers thereof
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/22—Acids obtained from polymerised unsaturated acids
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
- C10M2215/065—Phenyl-Naphthyl amines
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- 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
- C10M2219/085—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing carboxyl groups; Derivatives thereof
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- 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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- 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
- C10M2223/041—Triaryl phosphates
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- 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
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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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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- 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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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
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- Chemical & Material Sciences (AREA)
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- Lubricants (AREA)
Description
PATENTANWÄLTE . -4 C η / O η rPATENT LAWYERS. -4 C η / O η r
DR.-ING. VON KREISLER DR.-ING. SCHÖNWALD DR.-ING. TH. MEYER DR. FUES DR. -ING. BY KREISLER DR.-ING. SCHÖNWALD DR.-ING. TH. MEYER DR. FUES
KÖLN !,DEICHMANNHAUS .COLOGNE !, DEICHMANNHAUS.
Köln, den 23.1.1967 Pu/AxCologne, January 23, 1967 Pu / Ax
The British Petroleum Company Limited '., . Britannic House, Flnsbury öircus, London, E.C.2 (England) The British Petroleum Company Limited '., . Britannic House, Flnsbury öircus, London, EC2 (England)
Die Erfindung bezieht sich auf hydraulische Flüssigkeiten, die sich zum Einsatz bei tiefen Temperaturen eignen.The invention relates to hydraulic fluids, which are suitable for use at low temperatures.
Zum Einsatz bei tiefen Temperaturen geeignete hydraulische Flüssigkeiten sind u.a. zum Betrieb von Kränen erforderlich, die auf Fahrzeugen montiert sind, die in Gebieten mit kaltem Klima eingesetzt sind. In der Kälte brauchen die hydraulischen Systeme eine überaus lange Anwärmzeit, wenn hydraulische Flüssigkeiten mit schlechten Tieftemperatureigenschaften verwendet werden. Da die Kräne normalerweise nur kurzzeitig eingesetzt werden, ist eine lange Anwärmzeit ein großer Nachteil. Ferner findet während der Anwärmzeit Blasenbildung statt, die mit der Zeit den Wirkungsgrad der hydraulischen Pumpe ernstlich beeinträchtigen kann. Es gibt hydraulische Flüssigkeiten, die zum Gebrauch in Flugzeugmotoren entwickelt worden sind, jedoch sind diese hydraulischen Flüssigkeiten im allgemeinen ziemlich teuer. Die Erfindung ist nun auf e.ln billiges Produkt gerichtet, das sich zum Einsatz bei tiefen Temperaturen eignet.Hydraulic ones suitable for use at low temperatures Liquids are required, among other things, to operate cranes mounted on vehicles operating in areas with cold climates are used. In the cold they need hydraulic systems, if hydraulic fluids with poor low temperature properties be used. Since the cranes are normally only used for a short time, there is a long warm-up time a great disadvantage. It also takes place during the warm-up period Blistering takes place, which over time reduces the efficiency of the can seriously affect the hydraulic pump. There are hydraulic fluids that are used in aircraft engines have been developed, however, these are hydraulic Liquids are generally quite expensive. The invention is now directed to a cheap product that is suitable for use at low temperatures.
Gegenstand der Erfindung ist eine zum Einsatz bei tiefen Temperaturen geeignete hydraulische Flüssigkeit, die da-The invention relates to one for use at depths Hydraulic fluid suitable for temperatures, which
909834/1181909834/1181
durch gekennzeichnet ist, daß sie eine aus einem "denormalisierten" Gasöl bestehende Grundflüssigkeit enthält, der ein Verdickungsmittel und viskositätsindexverbesserndes Mittel vom Typ der Polyacrylate, Polymethacrylate oder Polyolefine in einer solchen Menge zugemischt ist, daß die hydraulische Flüssigkeit "bei 37,80C eine Viskosität im·- Bereich-von 5 bis 15, vorzugsweise 5 bis 10 und insbesondere 5 bis 7,5 öS hat.is characterized by in that it contains a "denormalized" from a gas oil existing base liquid that is admixed with a thickener and viscosity index improving agent of the type of polyacrylates, polymethacrylates or polyolefins in an amount such that the hydraulic fluid "at 37.8 0 C a Viscosity in the range from 5 to 15, preferably 5 to 10 and in particular 5 to 7.5 oS.
Als "(denormalisiertes Gasöl" wird eine durch Destillation von. Rohöl erhaltene Gasölfraktion bezeichnet, deren Normalparaffingehalt so weit gesenkt worden ist, daß das Produkt einen n-Paraffingehalt von weniger als 10 Gew.o-$, vorzugsweise von weniger als 5 Gew„-$ hat„ Die Verringerung des n-Paraffingeiialtes wird durch Behandlung mit einem Molekularsieb erreicht, jedoch können auch.andere Methoden, z„B. die Harnstoffadduktion, angewendet werden« Die verschiedensten Verfahren, bei denen Molekularsiebe verwendet werden, werden heute an vielen Stellen großtechnisch durchgeführt» Ihr Zweck ist die Abtrennung' von ziemlich reinen n-Paraffinen von den eingesetzten Erdölfraktionen, Die n-Paraffine sind gewöhnlich als Einsatzmaterial für die verschiedensten Verfahren zur Herstellung von chemischen Produkten erforderliche Wenn das Einsatzmaterial für einen Molekularsiebprozess, eine Gasölfraktion ist, fällt das als Nebenprodukt gebildete denormalisierte Gasöl häufig in so großen Mengen an, daß es nicht leicht abgesetzt werden kann» Gemäß der Erfindung wird eine zusätzliche Verwendung für dieses Material geschaffen, .. As a "(denormalized gas oil" a gas oil fraction obtained by distilling crude oil is referred to, the normal paraffin content has been reduced sufficiently that the product is an n-paraffin content of less than 10 wt o -. $, Preferably less than 5 wt "- "The reduction of the n-paraffin content is achieved by treatment with a molecular sieve, but other methods, such as urea adduction, can also be used." carried out »Their purpose is to separate 'fairly pure n-paraffins from the petroleum fractions used. The n-paraffins are usually required as a feedstock for a wide variety of processes for the manufacture of chemical products denormalized gas oil formed as a by-product often in such large quantities as that it cannot be easily removed »According to the invention, an additional use is created for this material,.
Das Verdickungsmittel und viskositätsindexverbessernde Mittel kann aus dem reinen Polymeren bestehen,: aber diese Mittel werden gewöhnlich als konzentrierte lösungen, (.wenigstens 25 Gewo-$) des Polymeren in einem. ■leichtenmin er a,*-· lischen Schmieröl verkauft* Diese Konzentr-äte. sind zur „ Verwendung in den erfindüngsgemäßen hydräUliiSehen -Plüssig-.fceitendurchaus -geeignete. Am zweckmäßigsten^ sind Polymere.The thickening agent and viscosity index improver may consist of the pure polymer: but these Remedies are usually given as concentrated solutions, (.at least 25 Gewo- $) of the polymer in one. ■ easymin er a, * - · ical lubricating oil sold * These concentrates. are to " Use in the hydraulic systems according to the invention, plus they are definitely used -suitable. Polymers are most useful.
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Konzentrate mit einer Viskositätszahl (gemäß der nachstehenden Definition) im Bereich von 3-150 ml/g, insbesondere 10-50 ml/go Gewöhnlich sind etwa 3-10 Gew,-/o des Verdickungsmittels und viskositätsindexverbessernden Mitia.s erforderlich,, um ein Gemisch mit der erforderlichen Viskosität im oben genannten Bereich zu erhalten, aber bereits 1 Gewc-^ kann bei Verwendung eines Mittels von sehr hoher Viskositätszahl genügen, um ein Gemisch mit niedriger Viskosität zu bilden, und eine Menge bis zu 70 Gew.-$ kann bei Verwendung eines Mittels mit sehr niedriger Viskositätszahl erforderlich sein, um ein Gemisch von hoher Viskosität zu bilden» Die in der hydraulischen Flüssigkeit verwendete Menge des Verdickungsmittels und ViskositätsindexverbesGerungsmittels sollte vorzugsweise genügen, um den Viskositätsindex der hydraulischen Flüssigkeit auf wenigstens 150 zu erhöhen,, · Concentrates with a viscosity number (as defined below) in the range of 3-150 ml / g, especially 10-50 ml / g mixture to obtain the required viscosity in the above range, but c already 1 wt - ^, when using a composition of very high viscosity sufficient to form a mixture having a low viscosity, and an amount up to 70 wt .- $ can when using an agent with a very low viscosity it may be necessary to form a mixture of high viscosity »The amount of thickener and viscosity index improver used in the hydraulic fluid should preferably be sufficient to increase the viscosity index of the hydraulic fluid to at least 150 ,, ·
Die "Viskositätszahl11 der Viskositätsindexverbesserer wird mit Hilfe der nachstehenden Formel ermittelt, wobei Viskosität swerte für ein denormalisiertes Gasöl und eine Lösung,, die aus dem denormalisierten Gasöl mit 5 g des Viskositätsindexverbesserers pro 100 ml Öl besteht, verwendet werden«,The "viscosity number 11 of the viscosity index improver is determined with the aid of the following formula, using viscosity values for a denormalized gas oil and a solution consisting of the denormalized gas oil with 5 g of the viscosity index improver per 100 ml of oil",
Tr. :, Λ. ..;.,_,, [Viskosität der Lösung b. 37.80O J Viskos^tatszahl = "1J. x Tr . :, Λ . ..;., _ ,, [ viscosity of the solution b. 37.8 0 OJ Viscosity number = " 1 J. x
Konzentration der Lösung in g/mlConcentration of the solution in g / ml
/'viskosität der Lösung bei 37»8°G -Λ ^Viskosität des 01s bei 37i8"0 " J / ' viscosity of the solution at 37 »8 ° G -Λ ^ viscosity of the oil at 37i8" 0 " J
Als Viskositätsindexverbesserer wird vorzugsweise ein polymerisierter Ester von Acryl- oder Methacrylsäure mit einem aliphatischen einwertigen Alkohol, der 4— 20 0-Atome im Molekül enthalt, verwendet* Produkte dieses Typs sind im Handel gewöhnlich als konzentrierte Lösungen des Polymeren in -mineralischen Schmierölen erhältlich«- Diese Lösun- A viscosity index improver is preferably used polymerized esters of acrylic or methacrylic acid with an aliphatic monohydric alcohol containing 4-20 0 atoms Contains in the molecule, used * are products of this type usually commercially available as concentrated solutions of the polymer in mineral lubricating oils "- these solutions
909834/1181909834/1181
BAD ORIGINALBATH ORIGINAL
gen haben eine Viskosität von 300-1000 öS bei 990O und von 2000-1QOOO öS bei -3T1Q0O. Ein Beispiel hierfür Bind die Produkte der Handelsbezeichnung "Aoryloid 150" und "Acryloid 710" (Hersteller Rohm «b Haas Company Limited). Geeignet Bind jedooh auch Polyolefine, insbesondere Polyisobutylen, beispielsweise das Produkt der Händelsbetedehnung "Paratone 210", eine konzentrierte Lösung von Polyisobutylen in einem mineralischen Schmieröl mit einer Viskosität von etwa 650 öS bei 990O (Hersteller Esso Petrolmm Company Limited)·genes have a viscosity of 300-1000 ÖS at 99 0 O and 2000-1QOOO ÖS at -3T 1 Q 0 O. An example of this bind the products with the trade name "Aoryloid 150" and "Acryloid 710" (manufacturer Rohm «b Haas Company Limited). However, polyolefins, in particular polyisobutylene, for example the product of Handel's stretching "Paratone 210", a concentrated solution of polyisobutylene in a mineral lubricating oil with a viscosity of about 650 OS at 99 0 O (manufacturer Esso Petrolmm Company Limited) are also suitable.
Die hydraulische Flüssigkeit gemäß der Erfindung enthält vorzugsweise 0*01-5 Gew.-^, insbesondere 0,05*· 1 öew.-# . eines Antioxydans. Am geeignetsten sind phenolieohe Anti-· oxydantien» insbesondere die eterieoh gehinderten Phenole, z.B. 2|6-l)i-tert.-butyl-p-kresol, 2,4.-Dimethyl-6-tert.-butylphenpüu und 4,4l-Methylen-bis(2,6-di-tert.-butylphenol)#, jedooh können auoh Aainverbindungen als Inhibitoren, z.B. Phenyl-a-naphthylamin und Phenyl-ß-naphthylamin, entweder allein oder in Kombination mit phenolisohen Antioxydantien zugesetzt werden.The hydraulic fluid according to the invention preferably contains 0 * 01-5% by weight, in particular 0.05 * * 1% by weight. an antioxidant. The most suitable are phenolic antioxidants, in particular the heterogeneous phenols, for example 2-6-1) i-tert-butyl-p-cresol, 2,4-dimethyl-6-tert-butylphenol and 4,4 1 -Methylene bis (2,6-di-tert-butylphenol) # , however, aline compounds can also be added as inhibitors, for example phenyl-α-naphthylamine and phenyl-β-naphthylamine, either alone or in combination with phenolic antioxidants.
Sehr zweckmäßig enthalten die hydraulischen flüssigkeiten außerdem eine geringe Menge von beispielsweise 0,01 bis 0,5 Gew.-# eines Rostinhibitors. Ale Rostinhibitoren eignen sich u.a.ÄUMnylbernsteinsäuren, AlkyImercaptotssigsäuren und Alkaryloxyessigsauren.The hydraulic fluids also very advantageously contain a small amount of, for example, 0.01 to 0.5 wt. # Of a rust inhibitor. All rust inhibitors are suitable ÄUMnylsuccinic acids, alkyl mercaptot acetic acids and alkaryloxyacetic acids.
Ein weiterer wertvoller Bestandteil, der in geringer Menge der hydraulischen Flüssigkeit zugesetzt werden kann, ist ein versohleißmindernder Zusatz· Als versohleißmindernde Zusätze eignen sich u.a. die Aryl- und Alkylphosphate mit bis zu 30 O-Atomen, z.B. Iritolylphosphat und· Trixylylphosphat, phoejihor-sulfurieierte Kohlenwasserstoffe, z.B. phosphor-Bulfqrisierte Terpene, und Zinkdithiophosphate der Formel(R10)(R20)PS.S.Zn.S.PS(OR3)(OR4), worin R1, R? f Br und R Alkyl-, Alkaryl- oder Arylreste mit 3-10 O-AtomenAnother valuable component that can be added to the hydraulic fluid in small quantities is an additive to reduce wear , for example phosphorus-sulfated terpenes, and zinc dithiophosphates of the formula (R 1 0) (R 2 0) PS.S.Zn.S.PS (OR 3 ) (OR 4 ), wherein R 1 , R ? f Br and R alkyl, alkaryl or aryl radicals with 3-10 O atoms
90983A/118190983A / 1181
sind« Die Menge liegt gewöhnlich zwischen 0,1 und 2 Gewo«-$.are "The crowd is usually between 0.1 and 2 percent o" - $.
Eine Anzahl von erfindungsgemäßen hydraulischen Flüssigkeiten, die sieh für den Einsatz bei tiefen !Temperaturen eignen» wurde aus den in Tabelle 1 genannten Bestandteilen hergestellt«A number of hydraulic fluids according to the invention which are intended for use at low temperatures suitable »was made up of the components listed in Table 1 manufactured"
Tabelle 1
Bestandteile (Gewo-#) Gemisch Table 1
Ingredients (wt o - #) mixture
Benormalisiertes Gasöl 94,27 93,27 93,27 94,27Benormalized gas oil 94.27 93.27 93.27 94.27
{Aoryloidi50 5,00 5*00{Aoryloidi 50 5.00 5 * 00
VI-Ve rbes serer (iorylald 7iiO 6,00VI Ve rbes serer (iorylald 7iiO 6.00
(ParatoiB 210 6,00(ParatoiB 210 6.00
Antioxydans % Antioxidant %
2,6-pi-terto~butyl-p- '2,6-pi-tert ~ butyl-p- o '
kresol 0,20 0,20 0,20 0,20cresol 0.20 0.20 0.20 0.20
Rostinhibit-or«Rust inhibitor "
Alkeny!bernsteinsäure 0,03 0,03 0,03 0,03Alkeny / succinic acid 0.03 0.03 0.03 0.03
Verschleißmindernde Zusatzes ; Trixylylphosphat 0,50 0,50 0,50Wear-reducing additive; Trixylyl phosphate 0.50 0.50 0.50
Lubrizol 810 0,50Lubrizol 810 0.50
Das denormalisierte Gasöl wurde erhalten, indem eine -Straight-run-Gasölfraktion, die einen Siedebereich von etwa 250-30O0O und einen n-Paraffingehalt von etwa 20 Gewo-$ hatte, mit einem 5A-Molekularsieb in bekannter Weise so behandelt wurde, daß ihr n-Paraffingehalt auf etwa 5 Gewo-^ erniedrigt wurde· ,The denormalized gas oil was obtained by a -Straight-run gas oil fraction of about 20 weight have a boiling range of about 250-30O 0 O and an n-paraffin content o - $ had been treated with a 5A molecular sieve in a known manner so that its n-paraffin content to about 5 wt o - ^ was lowered ·,
Die ViskositätBindexverbesserer, das Antioxydans, der Rostinhibitor und die verschleißmindernden Zusätase waren sämtlich im Handel erhältliche Produkteo The viscosity index improver, the antioxidant, the rust inhibitor and the wear reducing additives were all commercially available products or the like
909834/1181 BAD909834/1181 BATH
Des Produkt der Handelsbezeichnung "Acryloid 150" ist ein klares viskoses- Konzentrat eines Methacrylatpolymeren in einem raffinierten leichten Mid-Continent-Schmieröl einer Viskosität Ton 32 cS "bei 37980G. Das Produkt der Handelsbezeichnung "Acryloid 710" 1st ein klares-viskoses Konzentrat ©Ines Aorylpolymeren in einem hochwertigen lösungsmittelextrahierten neutralen Schmieröl. Das Produkt der Handelsbezeichnung "Paratone 210" ist ein Konzentrat eines linearen Xsobutylenpolymeren in einem Schmieröl. Die Kennzahian dieser Polymeren einschließlich ihrer Viskositätszahlen sind naohstehend in Tabelle 2 genannte Of the product of the trade name is "Acryloid 150", a clear viskoses- concentrate of a methacrylate in a refined light Mid-Continent-lubricating oil having a viscosity tone 32 cS "at 3798 0 G. The product of the trade designation" Acryloid 710 "1st a clear-viscous concentrate © Ines Aoryl polymers in a high quality solvent-extracted neutral lubricating oil. The trade name "Paratone 210" product is a concentrate of a linear xsobutylene polymer in a lubricating oil. The characteristics of these polymers, including their viscosity numbers, are given in Table 2 below
Viskosität des im Schmiei*-Viscosity of the in Schmiei * -
öl gelösten Stoffs bfisolute oil bfi
37,80G, öS 32 -37.8 0 G, öS 32 -
37,8°C-Viskosität der
Lösung in denormalisiertem Gasöl, die 5 g VI-Verbesserer
pro 100 ml
Öl enthält, cS 6,98 6,58 5,6137.8 ° C viscosity of the
Solution in denormalized gas oil containing 5 g VI improver per 100 ml
Oil contains, cS 6.98 6.58 5.61
Viskositätszahl ■ " 26,6 23,8 17,4Viscosity number ■ "26.6 23.8 17.4
* Bei Verdünnung mit 3 Gewe-!Deilen Mineralöl vom. Flammpunkt 2O4°C.* When diluted with 3 percent by e - Deilen oil from. Flash point 2O4 ° C.
Der Rostinhibitor war eine Alkeny!bernsteinsäure der Formel HOOCCH2Gh(R)COOH, worin R verschiedene verzweigtkettige aliphatische C.j2""Xohlenwasserstoffreste darstellt, die_ Je eine olefinische Doppelbindung enthalten»The rust inhibitor was an alkeny! Succinic acid of the formula HOOCCH 2 Gh (R) COOH, where R represents various branched-chain aliphatic hydrocarbon radicals which contain one olefinic double bond each »
909834/1 18»909834/1 18 »
BAD ORIGINALBATH ORIGINAL
Der verschleißmindernde Zusatz "Lubrizol 810" Ist ein phosphor- und eohwefelhaltiger Kohlenwaeseratoff· Der Schwefelgehalt dieses Zusatzes liegt im Bereich von 30-34· §eWe*-fS und der Phosphorgehalt im Bereich von 1 Tale 2The wear-reducing additive "Lubrizol 810" is a Phosphorus and eohulfurhaltiger Kohlenwaeseratoff · Der The sulfur content of this additive is in the range of 30-34 · §eWe * -fS and the phosphorus content in the range of 1 valley 2
.Verschiedene-Eigenschaften der Gemische A, B, O und B sind nachstehend in Tabelle 3 genannt. In Tabelle 3 sind auch die Ergebnisse von Belastungsprüfungen genannt, die mit den Gemischen A und D nach dem Vierkugeltest durchgeführt wurden, bei dem der Verschleiß, der durch eine rotierende Stahlkugel, die gegen einen Ring von drei fest eingespannten, mit der hydraulischen Flüssigkeit geschmierten Kugeln gepresst wird, für verschiedene Belastungen gemessen wird» Die Schweißbelastung ist die höchste Belastung, bei der noch keine Verschweißung der vier Kugeln stattfindete Die 2,5-Seko-Fressbelastung ist die niedrigste Belastung, bei der leichtes Fressen innerhalb von 2,5 Sekunden nach Beginn der Prüfung unter dieser Belastung tiaeetet· Die mittlere Hertz-Belastung wird aus der Größe der Anschliff -Fläche berechnet, die bei jeder Belastung gebildet wird. Die angewendete Methode war die gleiche, wie sie In US Federal Test Method Standard Nr. 791A Method 65OS ·1 Tom 27o7ο 1964- beschrieben ist mit der Ausnahme, daß die Bauer der Einzelversuche 1 Minute an Stelle von 10 Sekunden be- « trug und ausgewählte und keine vorgeschriebenen Prüfbelastungen angewendet wurden..Various properties of mixtures A, B, O and B are listed in Table 3 below. In Table 3 are also called the results of stress tests that with mixtures A and D according to the four-ball test, in which the wear caused by a rotating steel ball stuck against a ring of three clamped, with the hydraulic fluid lubricated balls is pressed, measured for different loads will »The welding load is the highest load at which the four balls have not yet welded together The 2.5 seco eating load is the lowest load in the case of light eating, tiaeetet within 2.5 seconds after the start of the test under this load The mean Hertz load is calculated from the size of the polished surface that is formed with each load will. The method used was the same as that used in In US Federal Test Method Standard No. 791A Method 65OS x 1 Tom 27o7ο 1964- is described with the exception that the farmer individual attempts last 1 minute instead of 10 seconds and selected and no prescribed test loads were applied.
9098 34/9098 34 /
(ungefähr)», öSViscosity bj-l7.8 0 0
(approximately) », öS
35*
35
Schale),0OFlash point (closed
Bowl), 0 O
mg KOH/gNeutralization number,
mg KOH / g
(Methode B)ASTM D665 rust test
(Method B)
Rostno
rust
Rostno
rust
Rostno
rust
Rostno
rust
kugeIpruf«erätExamination with the four
kugeIpruf «advises
lastung, kgMean Hertz Be
load, kg
lastung, kg2.5 sec -Preesbe-
load, kg
♦Sbctrajpoliert unter Verwendung einer graphisohen Darstellung von Viskosität in Abhängigkeit von der Temperatur.♦ Sbctraj polished using a graphical representation of viscosity as a function of temperature.
90983A/118190983A / 1181
Claims (1)
als 10 0@w»£ β&ϋ£ι&1£.l.) Hydraulic fluid according to claims 1 to 7, characterized in that it is a gas oil fractionator with an n-paraffin content of less than the denormalized gas oil
than 10 0 @ w »£ β & ϋ £ ι & 1 £.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3674/66A GB1167195A (en) | 1966-01-27 | 1966-01-27 | Low Temperature Hydraulic Fluid. |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1594365A1 true DE1594365A1 (en) | 1969-08-21 |
Family
ID=9762795
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19671594365 Pending DE1594365A1 (en) | 1966-01-27 | 1967-01-25 | Hydraulic fluid |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE693278A (en) |
DE (1) | DE1594365A1 (en) |
FR (1) | FR1509377A (en) |
GB (1) | GB1167195A (en) |
SE (1) | SE332040B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2524118A1 (en) * | 1974-05-31 | 1975-12-04 | Nippon Oil Co Ltd | HYDRAULIC FLUID FOR CENTRAL SYSTEMS |
DE2740449A1 (en) * | 1977-09-08 | 1979-03-29 | Roehm Gmbh | METHOD FOR PRODUCING LUBRICANT OILS |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070197410A1 (en) * | 2006-02-21 | 2007-08-23 | Rohmax Additives Gmbh | Energy efficiency in hydraulic systems |
US20080302422A1 (en) * | 2007-06-07 | 2008-12-11 | Rohmax Additives Gmbh | Power output in hydraulic systems |
WO2009024610A1 (en) * | 2007-08-23 | 2009-02-26 | Shell Internationale Research Maatschappij B.V. | Use of a lubricating oil composition |
-
1966
- 1966-01-27 GB GB3674/66A patent/GB1167195A/en not_active Expired
-
1967
- 1967-01-19 FR FR91815A patent/FR1509377A/en not_active Expired
- 1967-01-25 DE DE19671594365 patent/DE1594365A1/en active Pending
- 1967-01-27 SE SE01209/67A patent/SE332040B/xx unknown
- 1967-01-27 BE BE693278D patent/BE693278A/xx unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2524118A1 (en) * | 1974-05-31 | 1975-12-04 | Nippon Oil Co Ltd | HYDRAULIC FLUID FOR CENTRAL SYSTEMS |
DE2740449A1 (en) * | 1977-09-08 | 1979-03-29 | Roehm Gmbh | METHOD FOR PRODUCING LUBRICANT OILS |
Also Published As
Publication number | Publication date |
---|---|
FR1509377A (en) | 1968-01-12 |
GB1167195A (en) | 1969-10-15 |
BE693278A (en) | 1967-07-27 |
SE332040B (en) | 1971-01-25 |
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