DE2147416C2 - Wasserunempfindliche hydraulische Flüssigkeiten - Google Patents
Wasserunempfindliche hydraulische FlüssigkeitenInfo
- Publication number
- DE2147416C2 DE2147416C2 DE2147416A DE2147416A DE2147416C2 DE 2147416 C2 DE2147416 C2 DE 2147416C2 DE 2147416 A DE2147416 A DE 2147416A DE 2147416 A DE2147416 A DE 2147416A DE 2147416 C2 DE2147416 C2 DE 2147416C2
- Authority
- DE
- Germany
- Prior art keywords
- water
- hydraulic fluids
- weight
- boric acid
- glycol
- 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
Links
- 239000012530 fluid Substances 0.000 title claims description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 16
- -1 boric acid ester compound Chemical class 0.000 claims description 21
- 239000004327 boric acid Substances 0.000 claims description 15
- 239000003085 diluting agent Substances 0.000 claims description 5
- 239000000314 lubricant Substances 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 22
- 125000004432 carbon atom Chemical group C* 0.000 description 13
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 11
- 238000010992 reflux Methods 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- GTAKOUPXIUWZIA-UHFFFAOYSA-N 2-[2-[2-(2-ethoxyethoxy)ethoxy]ethoxy]ethanol Chemical compound CCOCCOCCOCCOCCO GTAKOUPXIUWZIA-UHFFFAOYSA-N 0.000 description 4
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 4
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 3
- 239000012964 benzotriazole Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 3
- 229940043276 diisopropanolamine Drugs 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical class CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- TUEYHEWXYWCDHA-UHFFFAOYSA-N ethyl 5-methylthiadiazole-4-carboxylate Chemical compound CCOC(=O)C=1N=NSC=1C TUEYHEWXYWCDHA-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 210000002837 heart atrium Anatomy 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
Classifications
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
- C10M111/04—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/04—Esters of boric acids
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- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/20—Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
- C10M107/30—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M107/32—Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
- C10M107/34—Polyoxyalkylenes
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- C10M125/20—Compounds containing nitrogen
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- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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- 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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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02M—SUPPLYING COMBUSTION ENGINES IN GENERAL WITH COMBUSTIBLE MIXTURES OR CONSTITUENTS THEREOF
- F02M1/00—Carburettors with means for facilitating engine's starting or its idling below operational temperatures
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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Description
R[O-R"1,OR'
worin
R eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen,
R' Wasserstoff oder eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen,
R" eine Alkylengruppe mit 2 bis 4 Kohlenstoffatomen und
y eine ganze Zahl von 2 bis 4
bedeuten, und gegebenenfalls
c) einem Polyoxyalkylenglykol mit einem Molekulargewicht von nicht weniger als etwa 150 bis 400 nach Patent 17 68 933
c) einem Polyoxyalkylenglykol mit einem Molekulargewicht von nicht weniger als etwa 150 bis 400 nach Patent 17 68 933
dadurch gekennzeichnet, daß der Gehalt an der Borsäureester-Verbindung 20 bis 44 Gewichtsprozent,
bezogen auf das Gesamtgewicht der Flüssigkeit, beträgt.
2. Hydraulische Flüssigkeit nach Anspruch 1, dadurch gekennzeichnet, daß der Gehalt an der Borsäureester-Verbindung
mindestens 30 Gewichtsprozent beträgt.
3. Hydraulische Flüssigkeit nach den Ansprüchen 1 und 2, dadurch gekennzeichnet, daß sie einen
Triester der Borsäure der nachstehenden allgemeinen Formel
worin
R eine Alkylgruppe mit 1 bis 4 C-Atomen,
R' Wasserstoff oder eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen,
R" cine Alkylengruppe mit 2 bis 4 Kohlenstoffatomen und
R' Wasserstoff oder eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen,
R" cine Alkylengruppe mit 2 bis 4 Kohlenstoffatomen und
y eine ganze Zahl von 2 bis 4
bedeuten. Vorzugsweise hat R" die Bedeutung von —(CH2)a, wobei χ eine ganze Zahl von 2 bis 4 ist
Überraschenderweise wurde nunmehr gefunden, daß sich der Anwendungsbereich von wasserunempfindlichen
hydraulischen Flüssigkeiten dieses Typs wesentlich verbreitern läßt, wenn man den Bereich für der. Gehalt
an der Borsäureester-Verbindung erweitert Insbesondere
hydraulische Flüssigkeiten mit einem Gehalt an der borhaltigen Verbindung im Bereich von etwa 20 bis
44 Gewichtsprozent weisen einen niedrigeren Siedepunkt auf als die hydraulischen Flüssigkeiten des Hauptpatents,
was für bestimmte Anwendungszwecke vorteilhaft ist Trotzdem wird aber der Siedepunkt durch die
Aufnahme von Wasser während des praktischen Gebrauchs, beispielsweise als Bremsflüssigkeit in Kraftwagen,
nicht in unerwünschter Weise so weit herabgesetzt, daß die vorgeschriebenen Sicherheitsgrenzen überschritten
würden.
Demgemäß betrifft die vorliegende Erfindung hydraulische Flüssigkeiten, bestehend aus wenigstens einer
als Schmiermittel wirkenden Borsäureester-Verbindung, einem Verdünnungsmittel der allgemeinen Formel
I
[R1(O- R,), -O]3- B
enthält, in welcher
Ri einen Alkylrest mit 1 bis 4 Kohlenstoffatomen
bedeutet,
R1, ein Alkylenrest mit 2 bis 4 Kohlenstoffatomen
R1, ein Alkylenrest mit 2 bis 4 Kohlenstoffatomen
ist und
y eine ganze Zahl von 2 bis 4 darstellt.
y eine ganze Zahl von 2 bis 4 darstellt.
4. Hydraulische Flüssigkeit nach den Ansprüchen 1 bis 3, dadurch gekennzeichnet, daß der Gehalt
an dem Verdünnungsmittel der allgemeinen Formel (I) bis zu 80 Gewichtsprozent, bezogen auf
das Gesamtgewicht der Flüssigkeit, beträgt.
Das Patent 17 68 933 betrifft wasserunempfindliche hydraulische Flüssigkeiten, bestehend aus etw 44 bis
Gewichtsprozent, bezogen auf das Gesamtgewicht der Flüssigkeit, an wenigstens einer als Schmiermittel
wirkenden Borsäureester-Verbindung, 0 bis etwa Gewichtsprozent, bezogen auf das Gesamtgewicht
der Flüssigkeit, wenigstens eines Polyoxyalkylenglykols mit einem Molekulargewicht von nicht weniger als 150
bis zu etwa 400, und etwa 3 bis etwa 50 Gewichtsprozent,
bezogen auf das Gesamtgewicht der Flüssigkeit, an wenigstens einem Verdünnungsmittel der allgemeinen
Formel
R[O-R1I1OR'
R[O-R"],OR'
worin
R eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen,
R' Wasserstoff oder eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen.
R' Wasserstoff oder eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen.
R" eine Alkylengruppe mit 2 bis 4 Kohlenstoffatomen und
y eine ganze Zahl von 2 bis 4
bedeuten, und gegebenenfalls einem Polyoxyalkylenglykol mit einem Molekulargewicht von nicht weniger
als etwa 150 bis 400 nach Patent 17 68 933, welche dadurch
gekennzeichnet sind, daß der Gehalt an der Borsäureester-Verbindung etwa 20 bis 44 Gewichtsprozent,
bezogen auf das Gesamtgewicht der Flüssigkeit, beträgi.
Aus der CH-PS 3 16 412 sind'zwar Bremsflüssigkeiten
für Kraftfahrzeuge bekannt, welche als Basisflüssigkeit mindestens einen Glykoläther bzw. ein Glykol enthalten
und deren Schmierfähigkeit durch einen Gehalt von 3 bis 10% einer Borsäureverbindung, wie eines Borsäureesters,
verbessert werden soll. Diese Literaturstelle vermittelt aber keine Lehre, wie hydraulische Flüssigkeiten
beschaffen sein müssen, die eine erhöhte Wasserfestigkeit aufweisen und den sehr strengen US-Bestimmungen
in bezug auf den Mindest-Siedepunkt bei einem Wassergehalt von 3,5 Gewichtsprozent entsprechen.
Auch die aus der DE-AS 12 95 124 bekannten Hydraulikflüssigkeiten auf Glykol- bzw. Glykolätherbasis mit einem Gehalt an Komplexverbindungen, die durch Umsetzen von Tetraboraten bzw. Metaboraten mit überschüssigem Glykol erhalten werden können, genügen diesen strengen Anforderungen nicht. Vergleichs-
Auch die aus der DE-AS 12 95 124 bekannten Hydraulikflüssigkeiten auf Glykol- bzw. Glykolätherbasis mit einem Gehalt an Komplexverbindungen, die durch Umsetzen von Tetraboraten bzw. Metaboraten mit überschüssigem Glykol erhalten werden können, genügen diesen strengen Anforderungen nicht. Vergleichs-
M versuche zeigten, daß derartige Hydraulikflüssigkeiten
einen zu niedrigen Siedepunkt im wasserhaltigen Zustand und außerdem eine relativ hohe Viskosität im Vergleich
zu erfindungsgemäßen Hydraulikflüssigkeiten
aufweisen.
Vorzugsweise beträgt der Gehalt an der Borsäureester-Verbindung
bei den erfindungsgemäßen hydraulischen Flüssigkeiten mindstens 30 Gewichtsprozent
Die erfindungsgemäßen Hydraulikflüssigkeiten zeichnen sich unter anderem dadurch aus, daß sie den
vom US-Department of Transportation in Betracht gezogenen Standardbedingungen für Bremsflüssigkeiten
entsprechen, d. h., daß sie bei einem Wasserzusatz bis zu
etwa 3,5 Volumenprozent einen Siedepunkt oberhalb 1600C im praktisch wasserfreien Zustand einen Siedepunkt
oberhalb 232,2° C aufweisen.
Weiterhin zeigen die erfindungsgemäßen Hydraulikflüssigkeiten nur eine geringe Korrosivität, und sie sind
gut mit Kautschuk verträglich, auch ohne einen Zusatz an kostspieligen Alkoholen, wie 2-Äthylhexanol, Heptanolen,
Glykolbutyläthern und Glykoldiäthern.
Die Borsäureester-Verbindungen leiten sich vorzugsweise
vun einem Glykolmonoäther ab, insbesondere handelt es sich dabei um Triester der Borsäure der nachstehenden
allgemeinen Formel
[R1(O-R1)^-O]3-B
Die erfindungsgemäßen Hydraulikflüssigkeiten können außerdem übliche Zusatzstoffe in Mengen bis zu
10 Gewichtsprozent enthalten, beispielsweise Antikorrosions- und Anti-oxydationsrr.ittel, Rostinhibitoren,
Antischaummittel, Stabilisatoren und Mittel zur Verbesserung des Viskositätsindex.
Die Beispiele erläuteren die Erfindung.
(II)
in welcher
Ri einen Alkylrest mit 1 bis 4 Kohlenstoffatomen bedeutet,
R3 einen Alkylenrest mit 2 bis 4 Kohlenstoffatomen
darstellt und
y eine ganze Zahl von 2 bis 4 ist.
Beispiele hierfür sind die folgenden Verbindungen:
[CH3(OCH2CH2)SO]3-B,
[C2Hä(OHC2CH2)2O]3-B,
[C2H5(OCH2CH2J3O]3-B,
[C2H5(OCH2CH2J4O]3- B,
[C3H7(OCH2CH2J3O]3-B,
[C4H9(OCH2CH2J2O]3-B und
[C4H9(OCH2CH2J3O]3-B.
Derartige Borsäueester lassen sich in an sich bekannter Weise aus Borsäure und den entsprechenden Glykoläthern
in Anwesenheit eines mit Wasser azeotrop abdestillierenden Lösungsmittels herstellen.
Im Rahmen der Erfindung können aber auch andere Typen von Borsäureester-Verbindungen eingesetzt
werden, wie sie auch in dem Hauptpatent 17 68 933 beschrieben
sind.
Das Verdünnungsmittel der vorstehend angegebenen Formel I wird zweckmäßig in Mengen bis zu 80 Gewichtsprozent,
bezogen auf das Gesamtgewicht der Flüssigkeit, eingesetzt. Wegen ihrer besonders g günstigen
Wirkung auf die Viskositätseigenschaften und das Wasseraufnahmevermögen werden die nachstehenden
Glykoläther bevorzugt:
Diäthylenglykolmonomethyläther,
Diäthylenglykolmonoäthyläther,
Diäthylenglykolmonobutyläther,
Triäthylenglykolmonomethyläther,
Triäthylenglykolmonoäthyläther,
Triäthylenglykolmonobutyläther,
Tetraäthylenglykolmonomethyläther,
Tetraäthylenglykolmonoäthyläther und
Tetraä thy lenglykolmonobu ty lather.
Gegebenenfalls können die erfindungsgemäßen Hydraulikflüssigkeiten zusätzlich auch Polyoxyalkylenglykole enthalten, deren Molekulargewicht vorzugsweise etwa 1OO bis 300 beträgt.
Gegebenenfalls können die erfindungsgemäßen Hydraulikflüssigkeiten zusätzlich auch Polyoxyalkylenglykole enthalten, deren Molekulargewicht vorzugsweise etwa 1OO bis 300 beträgt.
Beispiel 1 | Gewichts |
prozent | |
40,0 | |
[CH3(OCH2CH2J3O]3-B | 9,4 |
Tetraäthylenglykolmonoäthyläther | 50,01 |
Triäthylenglykolmonomethyläther | 0,5 |
Monoäthanolamin | 0,03 |
Benzotriazol | 0,06 |
Düsopropanolaminnitrit | 100,00 |
Eigenschaften: | |
Siedepunkt unter Rückfluß | 243,3° C |
(wasserfrei) | |
Siedepunkt unter Rückfluß | |
(wasserhaltig) | |
(3,5 ml Wasser | 171.rc |
+100 ml Hydraulikflüssigkeit) | 584 cS |
Viskosität bei -4O0C | |
Beispiel 2 | Gewichts |
prozent | |
30,0 | |
[CH3(OCH2CH2J3O]3-B | 7,0 |
Tetraäthylenglykolmonoäthyläther | 62,56 |
Triäthylenglykolmonomethyläther | 0,38 |
Monoäthanoiamin | 0,02 |
Benzotriazol | 0,04 |
Düsopropanolaminnitrit | 100,00 |
Eigenschaften: | |
Siedepunkt unter Rückfluß | 241,70C |
(wasserfrei) | |
Siedepunkt unter Rückfluß | |
(wasserhaltig) | |
(3,5 ml Wasser | 166,7° C |
+100 ml Hydraulikflüssigkeit) | 456 cS |
Viskosität bei -40°C | |
Beispiel 3 | Gewichts |
prozent | |
20,00 | |
[CH3(OCH2CH2)3O]3-B | 4,70 |
Tetraäthylenglykolmonoäthyläther | 75,01 |
Triäthylenglykolmonomethyläther | 0,25 |
Monoäthanolamin | 0,01 |
Benzotriazol | 0,03 |
Düsopropanolaminnitrit | 100,00 |
Eigenschaften: | |
Siedepunkt unter Rückfluß | 240° C |
(wasserfrei) | |
Siedepunkt unter Rückfluß | |
(wasserhaltig) | |
(3,5 ml Wasser | 161,7°C |
+ 100 ml Hydraulikflüssikgeit) | 373 cS |
Viskosität bei —400C | |
21 47 416 | 15 | 168,9° C | |
5 | |||
Beispiel 4 | |||
Gewichts | |||
prozent | |||
1H3(OCH2CH2J3O]3-B | 40,00 5 | ||
■iäthylenglykolmonomethyläther | 50,59 | ||
iäthanolamin | 1,78 | ||
>lyäthylenglykol (M. G. 300) | 7,62 | ||
atriumnitrit | 0,01 | ||
100,00 ,o | |||
genschaften: | |||
Siedepunkt unter Rückfluß | |||
(wasserfrei) | 239,4° C | ||
Siedepunkt unter Rückfluß | |||
(wasserhaltig) | |||
(3,5 ml Wasser | |||
+100 ml Hydraulikflüssigkeit |
20
25
30
45
50
55
60
Claims (1)
- Patentansprüche:
1. Hydraulische Flüssigkeit, bestehend auswenigstens einer als Schmiermittel wirkenden Borsäureester-Verbindung,
einem Verdünnungsmittel der allgemeinen Formel
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Publications (2)
Publication Number | Publication Date |
---|---|
DE2147416A1 DE2147416A1 (de) | 1973-07-26 |
DE2147416C2 true DE2147416C2 (de) | 1984-09-20 |
Family
ID=27585215
Family Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19681768133 Pending DE1768133A1 (de) | 1967-04-13 | 1968-04-04 | Kristallines Mannitol und Verfahren zu dessen Herstellung |
DE1768933A Expired DE1768933C3 (de) | 1967-04-13 | 1968-07-15 | Wasserunempfindliche hydraulische Flüssigkeiten |
DE2141441A Expired DE2141441C3 (de) | 1967-04-13 | 1971-08-18 | Wasserunempfindliche hydraulische Flüssigkeit |
DE2147416A Expired DE2147416C2 (de) | 1967-04-13 | 1971-09-22 | Wasserunempfindliche hydraulische Flüssigkeiten |
DE19762610934 Pending DE2610934A1 (de) | 1967-04-13 | 1976-03-16 | Vergaser fuer ottomotoren |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19681768133 Pending DE1768133A1 (de) | 1967-04-13 | 1968-04-04 | Kristallines Mannitol und Verfahren zu dessen Herstellung |
DE1768933A Expired DE1768933C3 (de) | 1967-04-13 | 1968-07-15 | Wasserunempfindliche hydraulische Flüssigkeiten |
DE2141441A Expired DE2141441C3 (de) | 1967-04-13 | 1971-08-18 | Wasserunempfindliche hydraulische Flüssigkeit |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19762610934 Pending DE2610934A1 (de) | 1967-04-13 | 1976-03-16 | Vergaser fuer ottomotoren |
Country Status (5)
Country | Link |
---|---|
US (6) | US3637794A (de) |
CA (2) | CA980756A (de) |
DE (5) | DE1768133A1 (de) |
FR (3) | FR2113788B1 (de) |
GB (8) | GB1232370A (de) |
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- 1968-04-04 DE DE19681768133 patent/DE1768133A1/de active Pending
- 1968-07-05 GB GB1232370D patent/GB1232370A/en not_active Expired
- 1968-07-05 GB GB1232369D patent/GB1232369A/en not_active Expired
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- 1968-07-15 DE DE1768933A patent/DE1768933C3/de not_active Expired
-
1970
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-
1971
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- 1971-04-12 US US00133407A patent/US3711412A/en not_active Expired - Lifetime
- 1971-04-15 US US00134456A patent/US3711411A/en not_active Expired - Lifetime
- 1971-05-17 CA CA113,158A patent/CA980756A/en not_active Expired
- 1971-05-17 CA CA113,157A patent/CA987656A/en not_active Expired
- 1971-05-20 GB GB1604471*[A patent/GB1354355A/en not_active Expired
- 1971-08-18 DE DE2141441A patent/DE2141441C3/de not_active Expired
- 1971-09-02 FR FR7131836A patent/FR2132617B2/fr not_active Expired
- 1971-09-22 DE DE2147416A patent/DE2147416C2/de not_active Expired
- 1971-11-20 GB GB1604371*[A patent/GB1382418A/en not_active Expired
-
1972
- 1972-01-20 GB GB3405071A patent/GB1384251A/en not_active Expired
- 1972-01-20 GB GB2513674A patent/GB1384685A/en not_active Expired
-
1976
- 1976-02-11 GB GB5263/76A patent/GB1531096A/en not_active Expired
- 1976-03-16 DE DE19762610934 patent/DE2610934A1/de active Pending
- 1976-04-14 FR FR7611004A patent/FR2307970A1/fr active Granted
Also Published As
Publication number | Publication date |
---|---|
US3625899A (en) | 1971-12-07 |
FR2132617A2 (de) | 1972-11-24 |
CA987656A (en) | 1976-04-20 |
GB1232369A (de) | 1971-05-19 |
US3711412A (en) | 1973-01-16 |
DE2610934A1 (de) | 1976-10-21 |
DE2147416A1 (de) | 1973-07-26 |
GB1354355A (en) | 1974-06-05 |
FR2307970B1 (de) | 1978-05-05 |
GB1214171A (en) | 1970-12-02 |
GB1382418A (en) | 1975-01-29 |
US3711411A (en) | 1973-01-16 |
DE2141441C3 (de) | 1987-12-03 |
FR2113788B1 (de) | 1974-08-23 |
DE1768933B2 (de) | 1977-11-10 |
DE1768933A1 (de) | 1972-04-20 |
DE1768133A1 (de) | 1971-09-02 |
DE2141441A1 (de) | 1973-08-16 |
DE2141441B2 (de) | 1981-07-23 |
DE1768933C3 (de) | 1982-09-16 |
FR2132617B2 (de) | 1975-07-11 |
GB1384685A (en) | 1975-02-19 |
US3637794A (en) | 1972-01-25 |
GB1232370A (de) | 1971-05-19 |
FR2307970A1 (fr) | 1976-11-12 |
FR2113788A1 (de) | 1972-06-30 |
GB1531096A (en) | 1978-11-01 |
US3711410A (en) | 1973-01-16 |
GB1384251A (en) | 1975-02-19 |
US3729497A (en) | 1973-04-24 |
DE1768133B2 (de) | 1974-04-04 |
CA980756A (en) | 1975-12-30 |
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