DE1078723B - Lubricating and hydraulic oils - Google Patents
Lubricating and hydraulic oilsInfo
- Publication number
- DE1078723B DE1078723B DER22853A DER0022853A DE1078723B DE 1078723 B DE1078723 B DE 1078723B DE R22853 A DER22853 A DE R22853A DE R0022853 A DER0022853 A DE R0022853A DE 1078723 B DE1078723 B DE 1078723B
- Authority
- DE
- Germany
- Prior art keywords
- moles
- lubricating
- carbon atoms
- alcohols
- hydraulic oils
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000010720 hydraulic oil Substances 0.000 title claims description 8
- 239000010687 lubricating oil Substances 0.000 title claims description 8
- 230000001050 lubricating effect Effects 0.000 title claims description 7
- 150000001298 alcohols Chemical class 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 238000007278 cyanoethylation reaction Methods 0.000 claims description 7
- 150000002009 diols Chemical class 0.000 claims description 7
- 230000032050 esterification Effects 0.000 claims description 6
- 238000005886 esterification reaction Methods 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
- 239000000047 product Substances 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000010696 ester oil Substances 0.000 description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- TVONJMOVBKMLOM-UHFFFAOYSA-N 2-methylidenebutanenitrile Chemical compound CCC(=C)C#N TVONJMOVBKMLOM-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- BIGPRXCJEDHCLP-UHFFFAOYSA-N ammonium bisulfate Chemical compound [NH4+].OS([O-])(=O)=O BIGPRXCJEDHCLP-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Schmier- und Hydrauliköle Zusatz zur Patentanmeldung R 21162 IVc / 23 c Gegenstand der Patentanmeldung R 21162 IV c/ 23 c ist die Verwendung von Verbindungen auf Esterbasis als Schmier- und Hydrauliköle, die nach an sich bekannten Verfahrensschritten durch Anlagerung von Acrylnitril, Methacrylnitril oder Äthacrylnitril bzw. Dimerisierungs- oder Oligomerisierungsprodukten dieser Nitrile an einwertige Alkohole mit mindestens 4 C-Atomen oder an mehrwertige Alkohole mit bis zu 10 C-Atomen, Verseifung der gebildeten Cyanäthylierungsprodukte und gleichzeitige Veresterung mit einwertigen, mindestens 4 C-Atome aufweisenden Alkoholen erhältlich sind. - Als besonders vorteilhaft haben sich für den genannten Verwendungszweck solche Ester erwiesen, die durch Veresterung der Cyanäthylierungsprodukte wenigstens zum Teil mit verzweigtkettigen Alkoholen erhalten worden sind.Lubricating and hydraulic oils Addendum to patent application R 21162 IVc / 23 c The subject of patent application R 21162 IV c / 23 c is the use of compounds based on esters as lubricating and hydraulic oils, which are made according to process steps known per se due to the addition of acrylonitrile, methacrylonitrile or ethacrylonitrile or dimerization or oligomerization products of these nitriles with monohydric alcohols with at least 4 carbon atoms or polyhydric alcohols with up to 10 carbon atoms, saponification of the formed Cyanoethylation products and simultaneous esterification with monovalent, at least Alcohols containing 4 carbon atoms are available. - Have been particularly beneficial those esters have been found for the stated purpose which are produced by esterification of the cyanoethylation products, at least in part, with branched-chain alcohols have been received.
Es wurde gefunden, daß eine weitere Verbesserung der als Schmier- und Hydrauliköle zu verwendenden Esteröle hinsichtlich des Querschnittes ihrer Eigenschaften erzielt werden kann, wenn die Veresterung der verseiften Cyanäthylierungsprodukte nach Patentanmeldung R 21162 IVc/23 c an Stelle von einwertigen Alkoholen mit mindestens 4 C-Atomen mit einem Gemisch aus einem Monoalkohol mit mindestens 4 C-Atomen und einem Diol bzw. aus mehreren solchen Monoalkoholen und Diolen durchgeführt worden ist.It has been found that a further improvement in the lubricant and hydraulic oils, ester oils to be used in terms of the cross section of their properties can be achieved if the esterification of the saponified cyanoethylation products according to patent application R 21162 IVc / 23 c instead of monohydric alcohols with at least 4 carbon atoms with a mixture of a monoalcohol with at least 4 carbon atoms and a diol or from several such monoalcohols and diols is.
Zu den für den genannten Zweck verwendbaren Produkten kann man auch derart kommen, daß man in erster Stufe partiell mit einem Monoalkohol und in zweiter Stufe mit einem- Diol verseift, oder umgekehrt. Für bestimmte Zwecke kann es vorteilhaft sein, ein Gemisch aus einem der erfindungsgemäßen Esteröle mit einem Esteröl der bereits bekannten oder vorgeschlagenen Art oder/und mit anderen Schmier-oder Hydraulikölen zu verwenden.The products that can be used for the stated purpose can also be come in such a way that one in the first stage partially with a mono alcohol and in the second Stage saponified with a diol, or vice versa. For certain purposes it can be beneficial be a mixture of one of the ester oils according to the invention with an ester oil of already known or proposed type and / or with other lubricating or hydraulic oils to use.
Als Beispiele der zur Herstellung der erfindungsgemäßen Schmiermittel verwendbaren Alkohole seien Monoalkohole, wie Dodecylalkohol, Decylalkohol, Octanol, oder Diole, wie Glykol, Propandiol, Butandiol, Hexandiol, Diäthylen- und Triäthylenglykol, und dreiwertige Alkohole, wie Glycerin, genannt.As examples of the preparation of the lubricants according to the invention Usable alcohols are monoalcohols, such as dodecyl alcohol, decyl alcohol, octanol, or diols such as glycol, propanediol, butanediol, hexanediol, diethylene and triethylene glycol, and trihydric alcohols such as glycerine.
Die Verseifung der aus einem Alkohol und einem Acrylnitril . entstandenen Cyanäthylierungsprodukte kann in an sich üblicher Weise in schwefelsaurer Lösung erfolgen.The saponification of an alcohol and an acrylonitrile. resulting Cyanoethylation products can be obtained in a conventional manner in sulfuric acid solution take place.
Im allgemeinen wird man die Verseifung und die mit zwei verschiedenen Alkoholen erfolgende Veresterung in einer Verfahrensstufe durchführen, und zwar derart, daß pro Nitrilgruppe im Cyanäthylierungsprodukt 1 Mol Wasser, etwa 1 Mol H2 S 04 und eine äquivalente Alkoholmenge umgesetzt wird. Das jeweilige Mengenverhältnis zwischen Monoalkohol und Diol soll dabei so bemessen sein, daß auf 1 Mol des zweiwertigen Alkohols mindestens 2 Mol des einwertigen Alkohols kommen. - Zu Produkten mit besonders günstigem Verhalten kommt man, wenn als veresternder, mindestens 4 Kohlenstoffatome im Molekül enthaltender Monoalkohol wenigstens zum Teil ein verzweigtkettiger Alkohol verwendet wird.In general, one will use saponification and that with two different ones Carry out esterification of alcohols in one process step, namely such that per nitrile group in the cyanoethylation product 1 mole of water, about 1 mole H2 S 04 and an equivalent amount of alcohol is implemented. The respective proportions between monoalcohol and diol should be measured so that 1 mole of the divalent Alcohol come at least 2 moles of the monohydric alcohol. - To products with special One comes to favorable behavior when the esterifying agent has at least 4 carbon atoms Monoalcohol contained in the molecule is at least partly a branched-chain alcohol is used.
Das beschriebene Aufbauprinzip läßt hinsichtlich der Auswahl der die Esteröle ergebenden Komponen-. ten und hinsichtlich des Mengenverhältnisses, in denen die veresternden Alkohole innerhalb des angegebenen Bereichs verwendet werden können, eine Vielzahl von Variationsmöglichkeiten zu. Das angegebene Aufbauprinzip ermöglicht es, Schmier- und Hydrauliköle für einen jeweiligen Verwendungszweck quasi »nach Maß« herzustellen.The construction principle described leaves with regard to the selection of the components resulting in the ester oils. th and with regard to the quantitative ratio in which the esterifying alcohols can be used within the specified range, a large number of possible variations. The specified construction principle makes it possible to produce lubricating and hydraulic oils for a particular application, quasi “made to measure ”.
Die im nachstehenden hinsichtlich ihrer Eigenschaften beschriebenen und im Sinne vorliegender Erfindung aufgebauten Esteröle wurden derart hergestellt, daß zunächst eine Anlagerung des ungesättigten Nitrils bzw. Dinitrils an einen Alkohol in Gegenwart von Lithiumhydroxyd als Katalysator erfolgte und die nicht umgesetzten Ausgangskomponenten nach Neutralisation des alkalischen Katalysators über eine Kolonne im Vakuum abgezogen wurden. Zu dem verbleibenden Rohprodukt wurde ein Gemisch aus einem Monoalkohol und einem Diol hinzugegeben, worauf diesem Gemisch die äquivalente Menge an Schwefelsäure und Wasser langsam zugesetzt wurde. Bei der unter dauerndem Rühren erfolgenden Abkühlung scheidet sich das gebildete Ammoniumbisulfat aus und wird durch Filtration abgetrennt. Die überschüssige Schwefelsäure wird mit Natriumcarbonat neutralisiert und das entstandene Natriumsulfat wiederum durch Filtration abgetrennt. Die unterhalb des Siedepunktes des erhaltenen Esteröles flüchtigen Bestandteile werden im Vakuum abgezogen; das verbleibende Produkt wird unmittelbar, gegebenenfalls nach dem bereits erwähnten Zusatz weiterer Schmiermittel oder üblicher Schmiermittelverbesserer, als Schmier- oder Hydrauliköl verwendet. Die Herstellung der erfindungsgemäß verwendeten Verbindungen auf Esterbasis wird im Rahmen vorliegender Erfindung nicht unter Schutz gestellt.Those described below with regard to their properties and ester oils structured in the sense of the present invention were produced in such a way that initially an addition of the unsaturated nitrile or dinitrile to an alcohol took place in the presence of lithium hydroxide as a catalyst and the unreacted Starting components after neutralization of the alkaline catalyst via a column were removed in vacuo. A mixture of was added to the remaining crude product added a monoalcohol and a diol, whereupon this mixture the equivalent Amount of sulfuric acid and water was slowly added. With the under permanent The ammonium bisulfate formed separates out and cools with stirring is separated off by filtration. The excess sulfuric acid is made with sodium carbonate neutralized and the sodium sulfate formed was again separated off by filtration. The one below of the boiling point of the ester oil obtained Components are removed in vacuo; the remaining product is immediately optionally after the already mentioned addition of further lubricants or more usual Lubricant improver, used as a lubricating or hydraulic oil. The production the ester-based compounds used according to the invention are described in the present context Invention not protected.
Beispiel Acrylnitril wurde an Glykol angelagert. Je 2 Mol des erhaltenen
Cyanäthylierungsproduktes wurden ver-
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DER22853A DE1078723B (en) | 1958-03-07 | 1958-03-07 | Lubricating and hydraulic oils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DER22853A DE1078723B (en) | 1958-03-07 | 1958-03-07 | Lubricating and hydraulic oils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1078723B true DE1078723B (en) | 1960-03-31 |
Family
ID=7401237
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DER22853A Pending DE1078723B (en) | 1958-03-07 | 1958-03-07 | Lubricating and hydraulic oils |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE1078723B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1112600B (en) | 1959-02-17 | 1961-08-10 | Roehm & Haas Gmbh | Lubricating and hydraulic oils |
-
1958
- 1958-03-07 DE DER22853A patent/DE1078723B/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1112600B (en) | 1959-02-17 | 1961-08-10 | Roehm & Haas Gmbh | Lubricating and hydraulic oils |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE833098C (en) | Low temperature greases | |
| DE906808C (en) | Process for the preparation of p-tert-octyl-arylphosphoric acid esters | |
| DE1053124B (en) | Additives and thickeners for lubricants based on mineral or synthetic lubricating oils | |
| DE69738570T2 (en) | CONCENTRATED AQUEOUS TENSID COMPOSITIONS OF BETAINTYP AND METHOD FOR THE PRODUCTION THEREOF | |
| DE1124935B (en) | Process for the production of mixtures of mixed esters with dicarboxylic acid esters, which are used as lubricants | |
| DE1593216B2 (en) | Non-ionic surface-active compounds and processes for their manufacture | |
| DE1668518A1 (en) | Process for the production of non-ionic surface-active substances derived from diols with a fatty acid chain | |
| DE1078723B (en) | Lubricating and hydraulic oils | |
| CH621592A5 (en) | ||
| DE3521711A1 (en) | Ester oils and their use | |
| DE3046443C2 (en) | Soap compositions with improved resistance to cracking | |
| DE1142982B (en) | Lubricant based on a dicarboxylic acid diester | |
| DE2062034B2 (en) | Use of synthetic esters as hydraulic fluids or as a component of hydraulic fluids | |
| DE975547C (en) | Process for the production of polycondensed phosphoric acid esters | |
| DE4444473A1 (en) | Water-in-oil emulsion explosives used in the mining industry | |
| AT156593B (en) | Process for the solidification of glycerine or glycerine substitutes. | |
| DE134165C (en) | ||
| DE741891C (en) | Process for the preparation of water-soluble nitrogen-containing condensation products | |
| AT221278B (en) | Process for the preparation of surface-active agents based on derivatives of polyalkylene glycols | |
| DE1444888C3 (en) | Grease | |
| DE187822C (en) | ||
| DE2144252C3 (en) | Process for the production of synthetic ester oils and their use | |
| DE260235C (en) | ||
| DE976907C (en) | Plasticizers for polymers that are made exclusively or mainly from vinyl chloride | |
| DE1043561B (en) | Aqueous solutions or emulsions for the non-cutting cold forming of metals |