EP0231524A2 - Application of alkylbenzoylacrylic acids as corrosion inhibitors - Google Patents
Application of alkylbenzoylacrylic acids as corrosion inhibitors Download PDFInfo
- Publication number
- EP0231524A2 EP0231524A2 EP86118106A EP86118106A EP0231524A2 EP 0231524 A2 EP0231524 A2 EP 0231524A2 EP 86118106 A EP86118106 A EP 86118106A EP 86118106 A EP86118106 A EP 86118106A EP 0231524 A2 EP0231524 A2 EP 0231524A2
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- EP
- European Patent Office
- Prior art keywords
- corrosion
- general formula
- mineral oil
- corrosion inhibitors
- compounds
- 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.)
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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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/28—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/38—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
- C10M129/40—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms monocarboxylic
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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
- 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
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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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
- 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
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
Definitions
- the invention relates to the use of 3- (p-alkyl-benzoyl) acrylic acid as a corrosion inhibitor in lubricating oils and greases based on mineral oils.
- DE-AS 11 49 843 discloses half-amides of saturated or unsaturated dicarboxylic acids and their salts with alphatic primary amines as additives for fuel oils and lubricating oils. Although these additives significantly improve corrosion protection, they have an extremely strong tendency to foam, which cannot be accepted in such additives.
- DE-AS 12 98 672 discloses alkali or amine salts of sulfonaminocarboxylic acids as corrosion inhibitors with good lubricating properties and little tendency to foam.
- the object of the present invention was to provide a new class of compounds which does not have the disadvantages of the prior art mentioned.
- the compounds should show a corrosion-inhibiting effect which is at least equivalent to the known corrosion inhibitors. They should also be ecologically and toxicologically safe. It has now been found that 3- (p-alkylbenzoyl) acrylic acids fully meet the requirements mentioned.
- the invention relates to the use of 3- (p-alkyl-benzoyl) acrylic acids of the general formula (I) in which R represents an alkyl radical having 8 to 18 carbon atoms or mixtures of several compounds of the general formula (I) as corrosion inhibitors in lubricating oils and lubricating greases based on mineral oils.
- 3- (p-alkylbenzoyl) acrylic acids of the general formula (I) are known from DE-OS 33 38 953.
- the e-g there named compounds have alkyl radicals R having from 1 to 6 carbon atoms, and are used as corrosion inhibitors in aqueous systems.
- alkylbenzenes of the general formula (II) in which R has the meanings given above are reacted with maleic anhydride in the course of a Friedel-Crafts acylation, the compounds of the general formula (I) used according to the invention being formed immediately in good yields and high purity.
- 3- (p-alkylbenzoyl) acrylic acids of the general formula (I) are used as corrosion inhibitors, in which R represents an alkyl radical having 8 to 18 carbon atoms.
- the alkyl radicals are therefore unbranched or branched radicals from the group octyl, Nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl and octadecyl in question, with straight-chain or branched alkyl radicals having 8 to 12 carbon atoms, ie Octyl, nonyl, decyl, undecyl and dodecyl radicals are preferred.
- the compounds of the general formula ( I ) mentioned can be used both individually and as a mixture with one another as anti-corrosion agents in lubricating oils and lubricating greases based on mineral oils, Ge mix two or more compounds of general formula (I) can be mixed in anti-corrosion agents.
- the compounds of general formula (I) mentioned or their mixtures can be used in aqueous solutions, dispersions or emulsions for corrosion protection agents. They are soluble in mineral oil at room temperature so that liquid concentrates can be produced. Their effectiveness is very high even in low concentrations. It has surprisingly been shown that amounts in the range between 0.005 and 10% by weight are sufficient to ensure excellent corrosion protection. The preferred application amounts are in the range from 0.1 to 1% by weight, based on the mineral oil base.
- the test procedure was carried out as follows: steel sheets of the quality 088 St-1405, the degreased and had been sanded, were in mineral oil samples (mineral oil. Pioneer 4556 (Fa naphthene) Hansen & R osenthel, Hamburg)) disappeared, the one V e r - bond of the general formula (I) as a corrosion inhibitor.
- the steel sheets were kept in brief contact with the mineral oil / anti-corrosion agent sample, then removed and after 24 hours of draining or drying time in the humidity chamber according to DIN 51359, in which the relative air humidity was 100% with a continuous air supply of 875 l / h and a temperature of 50 ° C. After the prescribed test period, the steel sheets were assessed for signs of corrosion.
- Example 1 steel sheets were immersed in identical mineral oil which did not contain any compound of the general formula (I) which could be used as a corrosion inhibitor held.
- the evaluation of signs of corrosion was carried out according to the same treatment method in accordance with the evaluation scale given in Example 1. The results are shown in Table 1 above.
- the concentration of the compounds of general formula (I) used as corrosion inhibitor in the mineral oil used is shown in Table 2 below. The evaluation was carried out on the evaluation scale given in Example 1.
Abstract
Description
Die Erfindung betrifft die Verwendung von 3-(p-Alkyl- benzoyl-)acrylsäure als Korrosionsschutzmittel in Schmierölen und Schmierfetten auf Mineralölbasis.The invention relates to the use of 3- (p-alkyl-benzoyl) acrylic acid as a corrosion inhibitor in lubricating oils and greases based on mineral oils.
In industriellen Prozessen, in denen Metalloberflächen, insbesondere Oberflächen aus Eisen und dessen Legierungen, unter extremen Bedingungen des Drucks und der Temperatur mit ölen oder ölhaltigen wässrigen Emulsionen in Verbindung kommen, tritt das Problem der Korrosion der Metalloberflächen auf. Als solche Prozesse sind beispielsweise großindustrielle Kühlprozesse, Metall-Oberflächenreinigung sowie Bearbeitungsprozesse der Metalloberflächen, wie Bohren, Schneiden, Walzen usw. zu verstehen. In derartigen Prozessen werden öle oder ölhaltige Emulsionen benutzt, ohne daß der Einfluß von Wasser auf die Metalloberfläche ganz ausgeschlossen werden kann. Die sukzessive Korrosion der mit den ölen oder ölhaltigen Flüssigkeiten in Kon- takt kommenden Metallteile führt jedoch zu einer deutlichen Reduzierung der Lebensdauer derartiger Anlagen bzw. zu Problemen bei der nachfolgenden Behandlung der Metalloberfläche, beispielsweise bei der Aufbringung einer korrosionsschützenden Oberflächenschicht durch Phosphatierung oder Lackierung.In industrial processes in which metal surfaces, in particular surfaces made of iron and its alloys, come into contact with oil or oil-containing aqueous emulsions under extreme conditions of pressure and temperature, the problem of corrosion of the metal surfaces occurs. Such processes are, for example, large-scale industrial cooling processes, metal surface cleaning and processing processes of the metal surfaces, such as drilling, cutting, rolling, etc. Can be used in such processes oils or oil emulsions are used without the influence d ate of water on the metal surface completely excluded. The gradual corrosion of n with the oil or oily liquids in co - but clock-coming metal parts leads to a significant reduction in the life of such equipment or to problems in the subsequent treatment of the Metal surface, for example when applying a corrosion-protective surface layer by phosphating or painting.
Es ist deswegen seit langer Zeit bekannt, den mit den Metalloberflächen in Kontakt kommenden Flüssigkeiten auf ölbasis Korrosionsinhibitoren zuzusetzen. Als solche kommen in überwiegend ölhaltigen Flüssigkeiten oder reinen ölen zahlreiche Verbindungen bzw. Gemische verschiedener Verbindung in-Frage. So werden in der DE-AS 11 49 843 als Zusatzmittel für Brennstofföle und Schmieröle Halbamide von gesättigten oder ungesättigten Dicarbonsäuren und deren Salze mit alphatischen primären Aminen offenbart. Diese Zusatzmittel verbessern zwar den Korrosionsschutz deutlich, weisen jedoch eine ausgesprochen starke Neigung zum Schäumen auf, die in derartigen Zusatzmitteln nicht akzeptiert werden kann. Alkali- oder Aminsalze von Sulfonaminocarbonsäuren als Korrosionsschutzmittel mit guter Schmierwirkung und geringer Neigung zum Schäumen werden in der DE-AS 12 98 672 offenbart. Diese Verbindungen enthaltende Mittel haben jedoch den Nachteil, daß ihre Herstellung nur in fabrikationstechnisch aufwendigen Prozessen möglich ist und sie infolge eines relativ hohen Gehalt: an Sulfonamidgruppen mitunter toxisch wirken oder zumindest toxische Wirkungen erwarten lassen, was entsprechende toxikologische Prü- ' fungen erforderlich macht.It has therefore been known for a long time to add corrosion inhibitors to the oil-based liquids which come into contact with the metal surfaces. As such, numerous compounds or mixtures of different compounds come into question in predominantly oil-containing liquids or pure oils. For example, DE-AS 11 49 843 discloses half-amides of saturated or unsaturated dicarboxylic acids and their salts with alphatic primary amines as additives for fuel oils and lubricating oils. Although these additives significantly improve corrosion protection, they have an extremely strong tendency to foam, which cannot be accepted in such additives. DE-AS 12 98 672 discloses alkali or amine salts of sulfonaminocarboxylic acids as corrosion inhibitors with good lubricating properties and little tendency to foam. These compounds products containing, however, have the disadvantage that their production is only possible in fabrication technically complicated processes and due to a relatively high level: sometimes toxic to sulfonamide or at least toxic effects expected let what appropriate toxicological Prü- 'levies requires.
Zur Korrosionsinhibierung in öl oder ölhaltigen Systemen sind aus Ullmann's Encyclopädie d. techn.Chem. Bd. 18, 4. Aufl. (1979) S. 1/2; Winnacker, Küchler, Chem. Technologie, Bd. 4 Org. Technologie II, 3. Aufl. (1972) S. 475 außerdem synthetische Sulfonate aus der Gruppe der Petrolsulfonate bekannt.For corrosion inhibition in oil or oil-containing systems from Ullmann's Encyclopedia d. Technical Chem. Vol . 18, 4th ed. (1979) p. 1/2; Winnacker, Küchler, Chem. Technologie, Vol. 4 Org. Technologie II, 3rd edition (1972) p . 475 synthetic sulfonates from the group of petroleum sulfonates are also known.
Nachteil dieser Verbindungsklasse ist jedoch, daß sie biologisch nicht abbaubar sind und damit in Prozessen, in denen zwangsläufig auch Umweltkontakt stattfindet, nicht einsetzbar sind, da ein Austritt derartiger Mittel in Abwässer oder in den Boden schwer übersehbare ökologische Schäden herbeiführen würde.The disadvantage of this class of compounds, however, is that they are not biodegradable and therefore cannot be used in processes in which environmental contact inevitably takes place, since leakage of such agents into wastewater or into the soil would cause ecological damage that is difficult to overlook.
Aufgabe der vorliegenden Erfindung war es, eine neue Klasse von Verbindungen zur Verfügung zu stellen, die die genannten Nachteile des Standes der Technik nicht aufweist. Die Verbindungen sollten eine den bekannten Korrosionsinhibitoren zumindest gleichwertige korrosionsinhibierende Wirkung zeigen. Außerdem sollten sie ökologisch und toxikologisch unbedenklich sein. Es wurde nun gefunden, daß 3-(p-Alkylbenzoyl-)acrylsäuren die genannten Anforderungen vollständig erfüllen.The object of the present invention was to provide a new class of compounds which does not have the disadvantages of the prior art mentioned. The compounds should show a corrosion-inhibiting effect which is at least equivalent to the known corrosion inhibitors. They should also be ecologically and toxicologically safe. It has now been found that 3- (p-alkylbenzoyl) acrylic acids fully meet the requirements mentioned.
Die Erfindung betrifft die Verwendung von 3-(p-Alkyl- benzoyl-)acrylsäuren der allgemeine Formel (I)
3-(p-Alkylbenzoyl-)acrylsäuren der allgemeinen Formel (I)
Die Herstellung derartiger Verbindungen erfolgt nach an sich bekannten Methoden. Beispielsweise können Alkylbenzole der allgemeinen Formel (II)
Erfindungsgemäß werden als Korrosionsschutzmittel 3-(p-Alkylbenzoyl-)acrylsäuren der allgemeinen Formel (I) verwendet, in der R für einen Alkylrest mit 8 bis 18 C-Atomen steht.-Als Alkylreste kommen somit unverzweigte oder verzweigte Reste aus der Gruppe Octyl, Nonyl, Decyl, Undecyl, Dodecyl, Tridecyl, Tetradecyl, Pentadecyl, Hexadecyl, Heptadecyl und Octadecyl in Frage, wobei geradkettige oder verzweigte Alkylreste mit 8 bis 12 C-Atomen, d.h. Octyl-, Nonyl-, Decyl-, Undecyl- und Dodecylreste bevorzugt sind.According to the invention, 3- (p-alkylbenzoyl) acrylic acids of the general formula (I) are used as corrosion inhibitors, in which R represents an alkyl radical having 8 to 18 carbon atoms. The alkyl radicals are therefore unbranched or branched radicals from the group octyl, Nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl and octadecyl in question, with straight-chain or branched alkyl radicals having 8 to 12 carbon atoms, ie Octyl, nonyl, decyl, undecyl and dodecyl radicals are preferred.
Die genannten Verbindungen der allgemeinen Formel (I) sind sowohl einzeln-als auch in Mischung miteinander als Korrosionschutzmittel-in Schmierölen und Schmierfetten auf Mineralölbasis verwendbar, wobei in Gemischen zwei oder auch mehrere Verbindungen der allgemeinen Formel (I) in Korrosionsschutzmitteln gemischt sein können.The compounds of the general formula ( I ) mentioned can be used both individually and as a mixture with one another as anti-corrosion agents in lubricating oils and lubricating greases based on mineral oils, Ge mix two or more compounds of general formula (I) can be mixed in anti-corrosion agents.
Die genannten Verbindungen der allgemeinen Formel (I) oder ihre Gemische können in wässrigen Lösungen, Dispersionen oder Emulsionen für Korrosionsschutzmittel verwendet werden. Sie sind bei Raumtemperatur in Mineralöl löslich, so daß flüssige Konzentrate hergestellt werden können. Ihre Wirksamkeit ist bereits in geringen Konzentrationen sehr hoch. Es hat sich nämlich überraschend gezeigt, daß Mengen im Bereich zwischen 0,005 und 10 Gew.-% ausreichend sind, um einen hervorragenden Korrosionsschutz sicherzustellen. Die bevorzugten Anwendungsmengen liegen im Bereich von 0,ol bis 1 Gew.-%, bezogen auf die Mineralölbasis.The compounds of general formula (I) mentioned or their mixtures can be used in aqueous solutions, dispersions or emulsions for corrosion protection agents. They are soluble in mineral oil at room temperature so that liquid concentrates can be produced. Their effectiveness is very high even in low concentrations. It has surprisingly been shown that amounts in the range between 0.005 and 10% by weight are sufficient to ensure excellent corrosion protection. The preferred application amounts are in the range from 0.1 to 1% by weight, based on the mineral oil base.
Die Erfindung wird durch die nachfolgenden Beispiele näher erläutert.The invention is illustrated by the following examples.
Prüfung von Verbindungen der allgemeinen Formel (I) als Rostschutzmittel in Mineralöl nach DIN 51359 (Feuchtigkeitskammer)Testing of compounds of general formula (I) as rust inhibitor in mineral oil according to DIN 51359 (humidity chamber)
Das Prüfverfahren wurde wie folgt durchgeführt: Stahlbleche der Qualität 088 St-1405, die entfettet und geschmirgelt worden waren, wurden in Mineralölproben (Mineralöl: Pionier 4556 (naphthenbasisch) der Fa. Hansen & Rosenthel, Hamburg)) getaucht, die eine Ver- bindung der allgemeinen Formel (I) als Korrosionsinhibitor enthielten. Die Stahlbleche wurden in kurzem Kontakt mit'der Mineralöl-/Korrosionsschutzmittel-Probe gehalten, danach entnommen und nach 24 h Abtropf- bzw. Trockendauer in die Feuchtigkeitskammer nach DIN 51359 gehängt, in der bei kontinuierlicher Luftzufuhr von 875 1/h und einer Temperatur von 50°C die relative Luftfeuchte 100-% betrug. Nach Ablauf der vorgeschrie- - benen Prüfdauer wurden die Stahlbleche auf Korrosionserscheinungen beurteilt.The test procedure was carried out as follows: steel sheets of the quality 088 St-1405, the degreased and had been sanded, were in mineral oil samples (mineral oil. Pioneer 4556 (Fa naphthene) Hansen & R osenthel, Hamburg)) disappeared, the one V e r - bond of the general formula (I) as a corrosion inhibitor. The steel sheets were kept in brief contact with the mineral oil / anti-corrosion agent sample, then removed and after 24 hours of draining or drying time in the humidity chamber according to DIN 51359, in which the relative air humidity was 100% with a continuous air supply of 875 l / h and a temperature of 50 ° C. After the prescribed test period, the steel sheets were assessed for signs of corrosion.
Die Prüfdauer in der Feuchtigkeitskammer sowie die Konzentration des Rostinhibitors im verwendeten Mineralöl sind aus der nachstehenden Tabelle 1 ersichtlich. Die Bewertung wurde wie folgt vorgenommen:
- 0: keine Korrosion;
- 1: Spuren von Korrosion;
- 2: leichte Korrosion (korrodierte Fläche ≤5 %);
- 3: mäßige Korrosion (korrodierte Fläche im Bereich zwischen 5 und 20 %); und
- 4: starke Korrosion (korrodierte Fläche >20 %).
- 0: no corrosion;
- 1: traces of corrosion;
- 2: slight corrosion (corroded area ≤5%);
- 3: moderate corrosion (corroded area in the range between 5 and 20%); and
- 4: severe corrosion (corroded area> 20%).
Entsprechend der in Beispiel 1 beschriebenen Vorgehensweise wurden Stahlbleche in identisches Mineralöl getaucht, das keine als Korrosionsinhibitor verwendbare Verbindung der allgemeinen Formel (I) enthielt. Die Bewertung auf Korrosionserscheinungen erfolgte nach gleicher Behandlungsweise entsprechend der in Beispiel 1 angegebenen Bewertungsskala. Die Ergebnisse sind der obigen Tabelle 1 zu entnehmen.In accordance with the procedure described in Example 1, steel sheets were immersed in identical mineral oil which did not contain any compound of the general formula (I) which could be used as a corrosion inhibitor held. The evaluation of signs of corrosion was carried out according to the same treatment method in accordance with the evaluation scale given in Example 1. The results are shown in Table 1 above.
Während die in Mineralöl mit einer Verbindung der allgemeinen Formel (I) getauchten Stahlbleche überwiegend keine oder höchstens leichte Korrosion (Korrosionsgrad bis 2) aufwiesen, zeigten Bleche, die in Mineralöl ohne Korrosionsinhibitor getaucht worden waren, ausnahmslos eine starke Korrosion. Starke Korrosionserscheinungen wurden auch schon nach kurzer Prüfdauer beobachtet.While the steel sheets immersed in mineral oil with a compound of the general formula (I) predominantly showed no or at most slight corrosion (degree of corrosion up to 2), sheets which had been immersed in mineral oil without a corrosion inhibitor showed strong corrosion without exception. Significant signs of corrosion were observed even after a short test period.
Stahlstäbe der Qualität CK 15, die entfettet und geschmirgelt worden waren, wurden einer Mineralöl-/Wasser-Rührprüfung nach DIN 51585 unterworfen. Dazu wurden sie bei 60°C in eine gerührte Mischung aus Mineralöl der Qualität analog Beispiel 1 und Wasser (Me-thode A) oder aus Mineralöl der Qualität analog Beispiel 1 und künstlichem Meerwasser (Methode B) für 24 h getaucht, wobei die Mineralöl-Wasser-Mischung mit einer Drehzahl von 1000 UpM gerührt wurde. Das Volumenverhältnis öl/Wasser betrug dabei 10 : 1.Steel bars of quality CK 15, which had been degreased and sanded, were subjected to a mineral oil / water stirring test in accordance with DIN 51585. To this end they were incubated at 60 ° C into a stirred mixture of mineral oil to the quality described in Example 1 and water (M e-Thode A) or of mineral oil to the quality described in Example 1 and artificial seawater (Method B) dipped for 24 h, wherein the mineral oil -Water mixture was stirred at a speed of 1000 rpm. The oil / water volume ratio was 10: 1.
Nach 24 h wurden die Stäbe der Mineralöl-Wasser-Mischung entnommen und auf Korrosionserscheinungen beurteilt.After 24 hours, the rods were removed from the mineral oil-water mixture and assessed for signs of corrosion.
Die Konzentration der als Korrosionsschutz-Inhibitor verwendeten Verbindungen der allgemeinen Formel (I) in dem verwendeten Mineralöl ist aus der nachstehenden Tabelle 2 ersichtlich. Die Bewertung wurde nach der in Beispiel 1 angegebenen Bewertungsskala vorgenommen.
Entsprechend der in Beispiel 2 angegebenen Methode wurden Stahlstäbe in Mineralöl getaucht, das keinen Korrcsionsinhibitor der allgemeinen Formel (I) enthielt. Dabei wurde sowohl eine Mischung aus Mineralöl der Qualität analog Beispiel 1 und Wasser (Methode A) als auch eine Mischung aus Mineralöl der Qualität analog Beispiel 1 und künstlichem Meerwasser (Methode B) verwendet. Die Ergebnisse sind ebenfalls der obigen Tabelle 2 zu entnehmen.In accordance with the method given in Example 2, steel rods were immersed in mineral oil which did not contain a corrosion inhibitor of the general formula (I). Both a mixture of mineral oil the quality analogous to example 1 and water (method A) and a mixture of mineral oil of the quality analogous to example 1 and artificial seawater (method B). The results are also shown in Table 2 above.
Im Korrosionstest nach DIN 51585 zeigen die Verbindungen der allgemeinen Formel (I) einen befriedigenden bis guten Korrosionsschutz in Mineralöl, insbesondere bei Konzentrationen ab 0,05 Gew.-%, bezogen auf Mineralölbasis. Im Gegensatz dazu werden identische Stahlstäbe durch Mineralöl-Wasser-Mischungen ohne Korrosionsinhibitor stark korrodiert.In the corrosion test according to DIN 51585, the compounds of the general formula (I) show satisfactory to good corrosion protection in mineral oil, in particular at concentrations from 0.05% by weight, based on mineral oil. In contrast, identical steel rods are heavily corroded by mineral oil-water mixtures without a corrosion inhibitor.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT86118106T ATE69060T1 (en) | 1986-01-09 | 1986-12-29 | USE OF ALKYL BENZOY LACRYLIC ACIDS AS CORROSION INHIBITORS. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19863600401 DE3600401A1 (en) | 1986-01-09 | 1986-01-09 | USE OF ALKYLBENZOYL ACRYLIC ACIDS AS CORROSION INHIBITORS |
DE3600401 | 1986-01-09 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0231524A2 true EP0231524A2 (en) | 1987-08-12 |
EP0231524A3 EP0231524A3 (en) | 1988-03-23 |
EP0231524B1 EP0231524B1 (en) | 1991-10-30 |
Family
ID=6291557
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP86118106A Expired - Lifetime EP0231524B1 (en) | 1986-01-09 | 1986-12-29 | Application of alkylbenzoylacrylic acids as corrosion inhibitors |
Country Status (9)
Country | Link |
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US (1) | US4752406A (en) |
EP (1) | EP0231524B1 (en) |
JP (1) | JPS62167396A (en) |
AT (1) | ATE69060T1 (en) |
AU (1) | AU583171B2 (en) |
CA (1) | CA1272476A (en) |
DE (2) | DE3600401A1 (en) |
ES (1) | ES2026453T3 (en) |
ZA (1) | ZA87119B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
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GB8918086D0 (en) * | 1989-08-08 | 1989-09-20 | Ciba Geigy | Coating compositions |
US5961662A (en) | 1994-09-13 | 1999-10-05 | Kao Corporation | Washing method and clothes detergent composition |
US6100226A (en) * | 1998-05-20 | 2000-08-08 | The Lubrizol Corporation | Simple metal grease compositions |
WO2001059833A1 (en) | 2000-02-08 | 2001-08-16 | Ibiden Co., Ltd. | Ceramic board for semiconductor production and inspection devices |
JP2001244320A (en) | 2000-02-25 | 2001-09-07 | Ibiden Co Ltd | Ceramic substrate and manufacturing method therefor |
US20060090393A1 (en) * | 2004-10-29 | 2006-05-04 | Rowland Robert G | Epoxidized ester additives for reducing lead corrosion in lubricants and fuels |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1149843B (en) * | 1958-01-07 | 1963-06-06 | Socony Mobil Oil Co Inc | Additive for fuel and lubricating oils |
DE3338953A1 (en) * | 1983-10-27 | 1985-05-09 | Henkel KGaA, 4000 Düsseldorf | USE OF CORROSION INHIBITORS IN AQUEOUS SYSTEMS |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1298672B (en) * | 1967-07-15 | 1969-07-03 | Hoechst Ag | Corrosion-preventing metalworking agent |
DE2123858A1 (en) * | 1971-05-13 | 1972-12-07 | ||
JPH0235737B2 (en) * | 1982-01-26 | 1990-08-13 | Mitsui Petrochemical Ind | BEETAAAROIRUAKURIRUSANNOSEIHO |
-
1986
- 1986-01-09 DE DE19863600401 patent/DE3600401A1/en not_active Withdrawn
- 1986-12-29 AT AT86118106T patent/ATE69060T1/en not_active IP Right Cessation
- 1986-12-29 EP EP86118106A patent/EP0231524B1/en not_active Expired - Lifetime
- 1986-12-29 DE DE8686118106T patent/DE3682272D1/en not_active Expired - Fee Related
- 1986-12-29 ES ES198686118106T patent/ES2026453T3/en not_active Expired - Lifetime
-
1987
- 1987-01-06 US US07/000,708 patent/US4752406A/en not_active Expired - Fee Related
- 1987-01-07 CA CA000526851A patent/CA1272476A/en not_active Expired - Fee Related
- 1987-01-08 ZA ZA87119A patent/ZA87119B/en unknown
- 1987-01-08 AU AU67428/87A patent/AU583171B2/en not_active Ceased
- 1987-01-09 JP JP62003914A patent/JPS62167396A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1149843B (en) * | 1958-01-07 | 1963-06-06 | Socony Mobil Oil Co Inc | Additive for fuel and lubricating oils |
DE3338953A1 (en) * | 1983-10-27 | 1985-05-09 | Henkel KGaA, 4000 Düsseldorf | USE OF CORROSION INHIBITORS IN AQUEOUS SYSTEMS |
Non-Patent Citations (1)
Title |
---|
CHEMICAL ABSTRACTS, Band 78, Nr. 12, 26. M{rz 1973, Seite 91, Zusammenfassung 80361s, Columbus, Ohio, US; K. BOWDEN et al.: " Structure-activity relations. II. Antibacterial activity of 3-benzoylacrylic acids and esters", & ADVAN. CHEM. SER. 1972, 114(Biol. Correl.-Hansch Approach, Symp.),130-40 * |
Also Published As
Publication number | Publication date |
---|---|
DE3682272D1 (en) | 1991-12-05 |
ES2026453T3 (en) | 1992-05-01 |
US4752406A (en) | 1988-06-21 |
EP0231524B1 (en) | 1991-10-30 |
AU6742887A (en) | 1987-07-16 |
ZA87119B (en) | 1987-08-26 |
DE3600401A1 (en) | 1987-07-16 |
JPS62167396A (en) | 1987-07-23 |
EP0231524A3 (en) | 1988-03-23 |
AU583171B2 (en) | 1989-04-20 |
ATE69060T1 (en) | 1991-11-15 |
CA1272476A (en) | 1990-08-07 |
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