DE1274775C2 - Feuerfestes schmieroel - Google Patents
Feuerfestes schmieroelInfo
- Publication number
- DE1274775C2 DE1274775C2 DE1965L0051528 DEL0051528A DE1274775C2 DE 1274775 C2 DE1274775 C2 DE 1274775C2 DE 1965L0051528 DE1965L0051528 DE 1965L0051528 DE L0051528 A DEL0051528 A DE L0051528A DE 1274775 C2 DE1274775 C2 DE 1274775C2
- Authority
- DE
- Germany
- Prior art keywords
- phosphate
- mud
- lubricating oil
- diphenyl
- corrosion
- 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
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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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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/08—Materials not undergoing a change of physical state when used
- C09K5/10—Liquid materials
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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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- 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
- C10M2207/129—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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- 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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- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
- C10M2211/024—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aromatic
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- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated compounds
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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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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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/041—Siloxanes with specific structure containing aliphatic substituents
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- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/04—Siloxanes with specific structure
- C10M2229/042—Siloxanes with specific structure containing aromatic substituents
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- C10M2290/00—Mixtures of base materials or thickeners or additives
- C10M2290/02—Mineral base oils; Mixtures of fractions
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Description
Schmierölgemische, die polychlorierte Diphenyle und Triarylpkosphate in Mengen von 20:80 bis
80:20 aufweisen, sind bekannt Sie werden wegen ihrer Feuerfestigkeit als Turbinenöle verwendet. Sie
haben aber den Nachteil, daß sie korrodieren und Schlamm bilden, wenn man sie dem ASTM-D-943-Turbinenöl-Oxydationsstabilitätstest
unterwirft. Diese Nachteile hat das erfindungsgemäße Mittel nicht.
Es wurde nämlich gefunden, daß die Verringerung des Phosphorsäureestergehaltes auf 3 % des Gemisches
mit dem polychlorierten Diphenyl gegebenenfalls in Gegenwart der üblichen Oxydations- bzw. Rostinhibitoren
ein Schmiermittel ergibt, das den vorstehend angegebenen ölgemischen hinsichtlich der Korrosionsfestigkeit
und Schlammbildung wesentlich überlegen ist, und ohne weiteres den Mindestanforderungen für
Turbinenöle des ASTM-D-943-Testes genügt.
Überraschenderweise weist das Schmiermittel, welches 3% Arylphosphorsäureester enthält, hinsichtlich
Druckbeständigkeit, wesentlich bessere Eigenschaften auf (vgl. die Kurven der Zeichnung, Höchstwert bei
etwa 3% Phosphorsäureestergehalt). Hier liegt offensichtlich ein synergistisches Zusammenwirken zwischen
dem Phosphorsäureester und dem polychlorierten Diphenyl in der angegebenen Menge vor. Eine verbesserte
Säurefestigkeit und verbesserte Eigenschaften hinsichtlich der Schlammbildung werden mit 3 % Triarylphosphat
erzielt.
Das polychlorierte Diphenyl kann trichloriertes Diphenyl, tetrachloriertes Diphenyl oder pentachloriertes
Diphenyl oder Mischungen dieser Diphenyle sein.
Der Phosphorsäureester kann irgendein flüssiges
Gemische (Gewicht, °/„)
Triarylphosphat der ortho-Phosphorsäure der Fonnel
(RO)3 = P = O sein, in der R ein monocyclischer
Arylrest, wie Phenyl, Tolyl, Xylenyl, Cumenyl, Äthylphenyl
ist; die drei R-Reste können gleich oder verschieden sein. Bevorzugt werden die Phosphorsäureester
des monocyclischen Aryls und Aryle, mit niederen Alkylsubstituenten, bei welchen das Alkyl Methyl oder
Äthyl ist Beispiele für bevorzugte Phosphorsäureester sind Triphenylphosphat, Tricresylphosphat Trixyle-
o nylphosphat, Phenyldicresylphosphat, Diphenylcresylphosphat,
Cyclohexyldicresylphosphat und n-Hexenyldicresylphosphat.
Den beanspruchten ölen können auch andere übliche Zusatzstoffe beigemischt werden, z. B.
Schaum- und P-ostinhibitoren, Antioxidantien und Mittel zum Verbessern des Viskositätsindex, jeweils
in Mengen von 0,1 bis 3 Gewichtsprozent oder bei Mitteln zur Verbesserung des Viskositätsindex in
Mengen von 2 bis 10%.
Um die synergistische Wirkung hinsichtlich der Beständigkeit der beanspruchten Mischung zu veranschaulichen,
wurden mehrere Versuche in einer Timken-Maschine durchgeführt und die Belastbarkeit
einer Reihe von vorstehend beschriebenen Schmiennittelmischungen gemessen. Diese Gemische
wiesen alle Triarylphosphatester in Mischung mit Tetrachlordiphenyl in dem kritischen Mengenbereich
von 1 bis 5 Gewichtsprozent auf; die Belastbarkeit wurde in ein Koordinatensystem eingetragen und eine
Reihe von Kurven erhalten, die in der Zeichnung dargestellt sind. Folgende Phosphatester wurden geprüft:
1. Tricresylphosphat, 2. Diphenylcresylphosphat, 3. Triphenylphosphat und 4. Trixylenylphosphat.
Die Prüfungen wurden nach der »Fed. Method
Std. 791a, Nr. 6505« durchgeführt. Wie sich aus den Kurven ergibt, war das Tricresylphosphat am besten,
dann folgte das Diphenylcresyl.
Weitere 18 Beispiele sind in Tabellenform zusammengefaßt, um die Wirkung einer niedrigen Konzentration
von 3 % des Phosphatesters bezüglich der Korrosionsfestigkeit und Schlammbildung zu zeigen,
die in einem gewissen Gegensatz zu der höheren Konzentration in dem polychlorierten Diphenyl steht,
wenn das Schmiermittel dem Standard-ASTM-D-943-Turbinenöl-Oxydationsstabilitätstest
unterworfen wird.
Gemisch
1 2 3
10 11
12 13 14 15 16 17 18
10
Trichi^riertes Diphenyl
Tetrachloriertes Diphenyl
Pentachloriertes Diphenyl
Tricresylphosphat
Trixylenylphosphat
Diphenylcresylphosphat
Tributylphosphat
Octyldiphenylphosphat
l-mono-Chlornaphthalin
di-tert.-Butyl-para-kresol
Calciumpetroleumsulf onat *)
Octa-decenyl-bernsteinsäure
Butylpolyacrylat(M.G. 10000) 5,0 5,0 5,0 5,0
74,4 84,4 89,4 91,4 95 91,4 91,4 90,4 90,4 91,4 91,4
3 5
0,5 0,5 0,5 0,5
0,1 0,1 0,1 0,1
0,1 0,1 0,1 0,1
41,4
3
3
91,4 40,439,4 38,4 39,4 90,9 50,050,0 50,0 50,0
0,5 0,5 0,5 0,5 0,5 0,5
0,1 0,1 0,1 0,1 0,1
0,1 0,1 0,1 0,1 0,1
0,05
5,0 5,0 5,0 5,0 5,0 5,0
5,0 5,0 5,0 5,0 5,0 5,0
0,5 1,0 2,0 3,0 2,0
0,5 0,5 0,5 0,5 0,5 0,5 0,5
0,1 0,1 0,1 0,1 0,1 0,1 0,1
5,0 5,0 5,0 5,0 5,0 5,0 5,0
♦) Ein Calciumsulfonat, das bei der Raffination von Mineralölen mittels Schwefelsäure odei z. B. als sulfoniertes Alkylbenzol erhalten wird.
Der Oxydationsstabilitätstest besteht darin, daß man Sauerstoff durch eine bestimmte Menge polierte
korrodierbare Metalle enthaltendes öl perlen läßt — bei den Versuchen war es eine Spule aus poliertem
Kupfer und Stahl — und die in dem Öl entwickelte
Acidität, die Korrosion des Metalls und die Menge gebildeten Schlammes mißt In der Tabelle I sind die
Zusammensetzungen der geprüften Schmiermittel und in Tabelle II die erhaltenen Versuchsergebnisse zusammengefaßt.
Tabelle | Π | Neutralisati | Neutralisati | Neutralisati | Hierzu | Neutralisati | Eisen- und Kupferspulen | Schlamm oder |
ASTM-TfSt D-943/54 | onszahl | onszahl nach | onszahl nach | onszahl nach | Abscheidungen | |||
Gemisch | vor dem Test | SOO Stunden | 1000 Stunden | 2000 Stunden | ||||
0,05 | 0,39 | 0,70 | Korrosion | Schlamm | ||||
0,10 | 0,50 | 0,82 | 1,05 | Korrosion | Schlamm | |||
1 | 0,05 | — | 0,17 | 0,39 | keine Korrosion | sehr wenig Schlamm | ||
2 | 0,04 | — | 0,14 | 0,29 | keine Korrosion | kein Schlamm | ||
3 | 0,05 | — | 0,20 | 0,52 | gerostetes Eisen | kein Schlamm | ||
4 | 0,06 | 0,87 | 1,02 | 1,77 | gerostetes Eisen | Schlamm | ||
5 | 0,08 | 0,74 | 0,95 | 1,21 | gerostetes Eisen | Schlamm | ||
6 | 0,07 | 0,92 | 1.11 | 1,92 | gerostetes Eisen | Schlamm | ||
7 | 0,08 | 0,82 | 0,99 | 1,42 | gerostetes Eisen | Schlamm | ||
8 | 0,09 | — | 0,25 | 0,51 | keine Korrosion | wenig Schlamm | ||
9 | 0,12 | — | 0,27 | 0,43 | keine Korrosion | kein Schlamm | ||
10 | 0,05 | — | 0,16 | 0,32 | keine Korrosion | kein Schlamm | ||
11 | 0,05 | — | 0,14 | 0,32 | keine Korrosion | kein Schlamm | ||
12 | 0,06 | — | 0,16 | 0,35 | keine Korrosion | kein Schlamm | ||
13 | 0,06 | — | 0,20 | 0,41 | keine Korrosion | sehr wenig Schlamm | ||
16 | 0,12 | — | 0,24 | 0,60 | keine Korrosion | kein Schlamm | ||
17 | 1 Blatt Zeichnungen | |||||||
18 | ||||||||
Claims (1)
- Patentanspruch:Feuerfestes Schmieröl, hydraulische Flüssigkeit und "Wärmeübertragungsmittel, bestehend aus polychloriertem Diphenyl, einem bekannten Triarylphosphat und üblichen Schmierölzusätzen, dadurch gekennzeichnet, daß die Mischung 3 Gewichtsprozent Triarylphosphat enthält.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE668430D BE668430A (de) | 1965-09-01 | ||
US466192A US3352780A (en) | 1965-06-23 | 1965-06-23 | Fire resistant-extreme pressure and hydrolysis resistant lubricant comprising polychlorinated diphenyl and triaryl phosphates |
GB36998/65A GB1133602A (en) | 1965-09-01 | 1965-08-27 | Improvements in or relating to fire-resistant liquids |
DE1965L0051528 DE1274775C2 (de) | 1965-09-01 | 1965-09-01 | Feuerfestes schmieroel |
NL6511657A NL6511657A (de) | 1965-09-01 | 1965-09-07 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1965L0051528 DE1274775C2 (de) | 1965-09-01 | 1965-09-01 | Feuerfestes schmieroel |
NL6511657A NL6511657A (de) | 1965-09-01 | 1965-09-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE1274775C2 true DE1274775C2 (de) | 1975-09-25 |
DE1274775B DE1274775B (de) | 1975-09-25 |
Family
ID=25986005
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1965L0051528 Expired DE1274775C2 (de) | 1965-06-23 | 1965-09-01 | Feuerfestes schmieroel |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE668430A (de) |
DE (1) | DE1274775C2 (de) |
GB (1) | GB1133602A (de) |
NL (1) | NL6511657A (de) |
-
0
- BE BE668430D patent/BE668430A/xx unknown
-
1965
- 1965-08-27 GB GB36998/65A patent/GB1133602A/en not_active Expired
- 1965-09-01 DE DE1965L0051528 patent/DE1274775C2/de not_active Expired
- 1965-09-07 NL NL6511657A patent/NL6511657A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
BE668430A (de) | |
NL6511657A (de) | 1967-03-08 |
GB1133602A (en) | 1968-11-13 |
DE1274775B (de) | 1975-09-25 |
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Legal Events
Date | Code | Title | Description |
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