High efficiency polyalkylene glycol lubricants for use in worm gears
Abstract
A polyalkylene glycol based lubricant composition that contains specified rust inhibitors and antioxidants has lowered operating temperature and is particularly suitable for use in worm drive gearboxes. The rust inhibitors consist of an N-acylo arcosine and an imidizole while the antioxidant consists of an alkylated diphenyl amine and a hindered phenol.

Term
Term ended
Expired 11 February 2025, 1.6 years ago.
- Priority
- Filed
- Granted
- Expired
- Today
4 claims: 4 independent, 0 dependent
- 1A lubricant composition suitable for use in gearboxes comprising:a major amount of a base oil consisting of polyalkylene glycol fluid or mixture of polyalkylene glycol fluids, and, based on the total weight of the composition, (a) from 0.1 to 1.0 wt% of a rust inhibiting composition consisting of (i) a N-acylsarcosine of the formula where R is an alkyl or alkenyl group of from 10 to 30 carbon atoms;and(ii) a 4,5-dihydroimidazole of the formula where R1 is an alkyl or alkenyl group of from 10 to 30 carbon atoms and R2 is a hydroxy alkyl group of from 1 to 6 carbon atoms;and(b) from 0.1 to 2.0 wt% of an antioxidant composition consisting of (iii) an alkylated diphenyl amine of the formula where R3 and R4 are independently alkyl groups of from 2 to 20 carbon atoms;and(iv) a hindered phenol of the formula where R5 and R6 are independently alkyl groups of from 3 to 9 carbon atoms, x is an integer of from 1 to 4, and y is an integer of from 1 to 4,wherein the weight ratio of (i):(ii) is in the range of 3:1 to 1:3 and wherein the weight ratio of(iii):(iv) is in the range of 3:1 to 1:3. Composition de lubrifiant appropriée pour être utilisée dans des boîtes à engrenages, comprenant: une quantité majeure d'une huile de base composée d'un fluide de polyalkylène glycol ou d'un mélange de fluides de polyalkylène glycol, et basée sur le poids total de la composition, (a) entre 0,1 % en poids et 1,0 % en poids d'une composition antirouille, composée de (i) une N-acylsarcosine de la formule: dans laquelle R est un groupe alkyle ou alcényle qui contient entre 10 et 30 atomes de carbone;et(ii) un 4,5-dihydroimidazole de la formule: dans laquelle R1 est un groupe alkyle ou alcényle qui contient entre 10 et 30 atomes de carbone, et R2 est un groupe hydroxyalkyle qui contient entre 1 et 6 atomes de carbone;et(b) entre 0,1 % en poids et 2,0 % en poids d'une composition anti-oxydante, composée de (iii) une diphénylamine alkylée de la formule: dans laquelle R3 et R4 sont des groupes alkyle indépendants qui contiennent entre 2 et 20 atomes de carbone;et(iv) un phénol entravé de la formule dans laquelle R5 et R6 sont des groupes alkyle indépendants qui contiennent entre 3 et 9 atomes de carbone, x est un nombre entier qui est compris entre 1 et 4, et y est un nombre entier qui est compris entre 1 et 4, dans laquelle le rapport de poids de (i):(ii) est compris dans la gamme de 3:1 à 1:3 et dans laquelle le rapport de poids de (iii):(iv) est compris dans la gamme de 3:1 à 1:3. Schmiermittelzusammensetzung, die zur Verwendung in Getriebegehäusen geeignet ist, umfassend: eine größere Menge eines Basisöls bestehend aus Polyalkylenglykolfluid oder einer Mischung von Polyalkylenglykolfluiden und, bezogen auf das Gesamtgewicht der Zusammensetzung, (a) 0,1 bis 1,0 Gew.-% einer Rostschutzzusammensetzung bestehend aus (i) einem N-Acylsarcosin mit der Formel in der R eine Alkyl- oder Alkenylgruppe mit 10 bis 30 Kohlenstoffatomen ist, und(ii) einem 4,5-Dihydroimidazol mit der Formel in der R1 eine Alkyl- oder Alkenylgruppe mit 10 bis 30 Kohlenstoffatomen und R2 eine Hydroxyalkylgruppe mit 1 bis 6 Kohlenstoffatomen ist, und(b) 0,1 bis 2,0 Gew.-% einer Antioxidanszusammensetzung bestehend aus (iii) einem alkylierten Diphenylamin mit der Formel in der R3 und R4 unabhängig voneinander Alkylgruppen mit 2 bis 20 Kohlenstoffatomen sind, und(iv) einem gehinderten Phenol mit der Formel in der R5 und R6 unabhängig voneinander Alkylgruppen mit 3 bis 9 Kohlenstoffatomen sind, x eine ganze Zahl von 1 bis 4 ist und y eine ganze Zahl von 1 bis 4 ist,wobei das Gewichtsverhältnis von (i):(ii) im Bereich von 3:1 bis 1:3 liegt und das Gewichtsverhältnis von (iii):(iv) im Bereich von 3:1 bis 1:3 liegt.
- 2Composition selon la revendication 1, dans laquelle le polyalkylène glycol présente une viscosité qui est comprise dans la gamme de 50 cSt à 3000 cSt à 40°C. The composition of claim 1 wherein the polyalkylene glycol has a viscosity in the range of 50 to 3 000 cSt at 40°C. Zusammensetzung nach Anspruch 1, in der das Polyalkylenglykol eine Viskosität im Bereich von 50 bis 3000 cSt bei 40°C besitzt.
- 3Composition selon la revendication 1, dans laquelle l'huile de base est un mélange de fluides de polyalkylène glycol. The composition of claim 1 wherein the base oil is a mixture of polyalkylene glycol fluids. Zusammensetzung nach Anspruch 1, bei der das Basisöl eine Mischung von Polyalkylenglykolfluiden ist.
- 4Composition selon la revendication 1, contenant une quantité effective d'un additif anti-usure de phosphorothioate de phénol et d'un agent passivant de métal à base de tolyle triazole. The composition of claim 1 including an effective amount of a phenyl phosphorothioate antiwear additive and a tolyl triazole metal passivator. Zusammensetzung nach Anspruch 1, die eine wirksame Menge eines Phenolphosphortioat-Antiabriebadditivs und eines Tolyltriazol-Metallpassivierungsmittels enthält.
Independent claims4
32 paragraphs in 8 sections, as filed
FIELD OF INVENTION
The present invention relates generally to polyalkylene glycol (PAG) lubricants and specifically to improved food grade lubricants suitable for use in worm drive gearboxes and other mechanical devices where improved efficiency and lowered operating temperatures are desirable.
BACKGROUND OF INVENTION
As is well known, commercially available lubricant compositions are prepared from a variety of natural or synthetic base stocks or blends of base stocks combined with various additive packages and solvents depending upon their intended application. For example, polyalkylene glycol (PAG) fluids have found use as the base oil in gearbox lubricants because of their better oxidation stability at high temperature when compared to mineral lubricating oils. Notwithstanding the oxidation stability of polyalkylene glycols, lubricating compositions based on these fluids are formulated with various additives such as antioxidants, corrosion inhibitors and the like to provide enhanced performance of the lubricating composition.
Formulating lubricating compositions to meet ever more stringent requirements is quite complex because of the potential interactions that may occur between the various additives that may be employed. Indeed, experience has shown that incorporation of one type of additive in a lubricant composition can have a negative impact on the function of another type of additive in that composition. For example, the presence of antiwear additives in a lubricant often reduces the oxidation stability of the formulation compared to one in which the antiwear additive is absent. Because oxidative degradation of oils increases with increasing temperature there is a need for lubricating composition that possess lowered oil temperatures under conditions of use.
Thus, one object of the present invention is to provide lubricating composition having lowered oil temperatures under conditions of use.
Another object of the invention is to provide a high efficiency polyalkylene glycol based oil composition for use in worm gears.
Yet another object of the invention is to provide food grade lubricants, i.e., lubricant compositions composed of components that are approved by U.S. DEPARTMENT OF AGRICULTURE or the National Sanitary Foundation (NSF).
SUMMARY OF INVENTION
According to one embodiment of the invention a lubricant composition suitable for use in gearboxes comprises a major amount of a polyalkylene glycol base oil and, based on the total weight of the composition, <ol id="ol0001" compact="compact" ol-style=""><li>(a) from 0.1 to 1.0 wt% of a rust inhibiting composition consisting of <ol id="ol0002" ol-style=""><li>(i) a N-acylsarcosine of the formula <chemistry id="chem0001" num="0001"><img file="EP1733010B2_D0001.tif" /></chemistry> where R is an alkyl or alkenyl group of from 10 to 30 carbon atoms; and</li><li>(ii) 4,5-dihydroimidazole of the formula <chemistry id="chem0002" num="0002"><img file="EP1733010B2_D0002.tif" /></chemistry> where R<sub>1</sub> is an alkyl or alkenyl group of from 10 to 30 carbon atoms and R<sub>2</sub> is a hydroxy alkyl group of from 1 to 6 carbon atoms; and</li></ol></li><li>(b) from 0.1 to 2.0 wt% of an antioxidant composition consisting of <ul id="ul0001" list-style="none"><li>(iii) an alkylated diphenyl amine of the formula <chemistry id="chem0003" num="0003"><img file="EP1733010B2_D0003.tif" /></chemistry> where R<sub>3</sub> and R<sub>4</sub> are independently alkyl groups of from 2 to 20 carbon atoms; and</li><li>(iv) a hindered phenol of the formula <chemistry id="chem0004" num="0004"><img file="EP1733010B2_D0004.tif" /></chemistry> where R<sub>5</sub> and R<sub>6</sub> are independently alkyl groups of from 3 to 9 carbon atoms, x is an integer of from 1 to 4, and y is an integer of 1 to 4 wherein the weight ratio of (i):(ii) is in the range of 3:1 to 1:3 and wherein the weight ratio of (iii):(iv) is in the range of 3:1 to 1:3.</li></ul></li></ol>
A preferred lubricant composition includes an effective amount of a phenyl phosphorothioate antiwear additive and a tolyl triazole metal passivator.
Other aspects and embodiments of the invention will become apparent from the detailed description which follows.
BRIEF DESCRIPTION OF THE DRAWING
The accompanying figure is a graph showing the sump oil temperature over time in a gearbox operated with a commercially available polyalkylene glycol (PAG) oil and with the lubricating oil composition of the invention.
DETAILED DESCRIPTION OF INVENTION
The composition of the invention comprises a major amount of a polyalkylene glycol fluid of lubricating viscosity. Suitable polyalkeylene glycol fluids are copolymers of alkylene oxides. Especially suitable are copolymers of ethylene oxide and propylene oxide.
The kinematic viscosity of the fluids used typically will be in the range of 50 cSt to 3000 cSt at 40°C depending, of course, upon the intended use of the ultimate composition. For example, for gearboxes the preferred kinematic viscosity of the fluid will be in the range of 135 to 1100 cSt at 40°C.
A single polyalkylene glycol fluid or a mixture of two or more polyalkylene glycol fluids may be used as the base oil in the invention composition to attain a desired viscosity.
The compositions also contain from 0.1 to 1.0 wt%, based on the total composition, of a rust inhibiting composition consisting of <ul id="ul0002" list-style="none"><li>(i) a N-acylsarcosine of the formula <chemistry id="chem0005" num="0005"><img file="EP1733010B2_D0005.tif" /></chemistry> where R is an alkyl or alkenyl group of from 10 to 30 carbon atoms; and</li><li>(ii) 4,5-dihydroimidazole of the formula <chemistry id="chem0006" num="0006"><img file="EP1733010B2_D0006.tif" /></chemistry> where R<sub>1</sub> is an alkyl or alkenyl group of from 10 to 30 carbon atoms and R<sub>2</sub> is a hydroxy alkyl group of from 1 to 6 carbon atoms.</li></ul>
In the practice of the invention the weight ratio of (i): (ii) will be in the range of 3:1 to 1:3 and more preferably 1:1. Also, it is preferred that R<sub>1</sub> is an alkenyl group of 12 to 20 carbon atoms and especially 18 carbon atoms, and that R<sub>2</sub> is a hydroxy alkyl group having 2 carbon atoms.
The lubricating composition of the invention also includes from 0.1 to 2.0 wt%, based on the total compostion, of an antioxidant composition consisting of: <ul id="ul0003" list-style="none"><li>(iii) an alkylated diphenyl amine of the formula <chemistry id="chem0007" num="0007"><img file="EP1733010B2_D0007.tif" /></chemistry> where R<sub>3</sub> and R<sub>4</sub> are independently alkyl groups of from 2 to 20 carbon atoms; and</li><li>(iv) a hindered phenol of the formula <chemistry id="chem0008" num="0008"><img file="EP1733010B2_D0008.tif" /></chemistry></li></ul> where R<sub>5</sub> and R<sub>6</sub> are independently alkyl groups of from 3 to 9 carbon atoms, x is an integer of from 1 to 4, and y is an integer of from 1 to 4.
The weight ratio of (iii) to (iv) in the range of 3:1 to 1:3 and more preferably 1:1. Additionally it is preferred that R<sub>3</sub> and R<sub>4</sub> are alkyl groups of 4 to 8 carbon atoms, that R<sub>5</sub> and R<sub>6</sub> are tert butyl groups, that x is 2, and y is from 2 to 4 and especially 3.
As will be demonstrated hereinafter, lubricant additives may increase the operating temperature of a composition containing them. Consequently where operating temperatures are of particular concern such as in gearboxes, it is especially preferred that the compositions of the invention less than 1.0 wt% of the rust inhibiting composition. For example, from 0.40 to 0.80 wt% and less than 2.0 wt% of the antioxidant composition, for example from 0.50 to 1.50 wt%, the wt% in all instances based on the total weight of the composition.
The lubricating composition of the present invention preferably will contain an effective amount of a phenyl phosphorothioate antiwear additive and a tolyltriazole metal passivator.
The phenyl phosphorothioate antiwear additive is represented by the formula: <chemistry id="chem0009" num="0009"><img file="EP1733010B2_D0009.tif" /></chemistry> where R<sub>7</sub> is H or an alkyl group of from 1 to 8 carbon atoms. Preferably R<sub>7</sub> is H. In general the amount of the antiwear additive will be in the range of 0.1 to 1.0 wt% based on the total weight of the lubricating composition.
The metal passivator may be represented by the formula: <chemistry id="chem0010" num="0010"><img file="EP1733010B2_D0010.tif" /></chemistry> where R<sub>8</sub> is a branched alkyl group of from 2 to 20 carbon atoms and preferably is <chemistry id="chem0011" num="0011"><img file="EP1733010B2_D0011.tif" /></chemistry>
In general the amount of the metal passivator will be in the range of 0.01 to 0.50 wt% based on the total weight of the lubricating composition.
Other additives may be used as well such as colorants, antifoamants, dispersants and the like.
The compositions of the invention are particularly useful in gearboxes but may also be used in other mechanical devices where metal free lubricants are preferred. Examples include screw and reciprocating compressors, vane pumps, turbine support bearings and the like.
Also it will be appreciated that the base fluid and additives of the inventive compositions are used in amounts that meet standards set by the USDA and the NSF and hence may properly be considered to be food grade lubricants suitable for use where at least incidental contact with food for human consumption is possible.
The invention will be further illustrated by the following examples in which all the amounts in wt% are based on the total weight of the lubricating compositions.
The test rig used in the following examples was a worm drive gearbox having a 4.45cm (1.75 inch) centerline distance and a 20:1 reduction ratio. The rig was operated at 100% rated load. The input power and torque as well as the output power and torque were monitored over a multi-hour test.
EXAMPLE 1
The test rig described above was run with a polyalkylene glycol fluid formulated with antiwear, metal passivator and defoamant ("Base Lube") and the sump temperature of the oil was determined after equilibrium. At periodic intervals a rust inhibitor consisting of a mixture of equal parts by weight of Sarkosyl-O and Amine-O, a N-acyl sarcosine and an amine respective, sold by Ciba of Norwich, CT was added to the oil in four doses of 0.5 wt% until a total of 2.0 wt% was added. The sump temperature at equilibrium for each additive was determined. The results are given in Table 1. <tables id="tabl0001" num="0001"><table frame="none"><title><u>TABLE 1</u></title><tgroup cols="3" colsep="0"><colspec colnum="1" colname="col1" colwidth="24mm" /><colspec colnum="2" colname="col2" colwidth="33mm" /><colspec colnum="3" colname="col3" colwidth="34mm" /><thead><row><entry align="center" valign="top">Component</entry><entry align="center" valign="top">Concentration, wt%</entry><entry align="center" valign="top">Temperature, °C (°F)</entry></row></thead><tbody><row rowsep="0"><entry align="center" /><entry align="center" /><entry align="center" /></row><row rowsep="0"><entry>Base Lube</entry><entry align="center">0.00</entry><entry align="center">72.17 (161.9)</entry></row><row rowsep="0"><entry>Rust Inhibitor</entry><entry align="center">0.50</entry><entry align="center">72.50 (162.5)</entry></row><row rowsep="0"><entry>Rust Inhibitor</entry><entry align="center">1.00</entry><entry align="center">72.94 (163.3)</entry></row><row rowsep="0"><entry>Rust Inhibitor</entry><entry align="center">1.50</entry><entry align="center">73.00 (163.4)</entry></row><row rowsep="0"><entry>Rust Inhibitor</entry><entry align="center">2.00</entry><entry align="center">73.39 (164.1)</entry></row></tbody></tgroup></table></tables> As can be seen, increasing amounts of the additive results in increased temperature.
EXAMPLE 2
The procedure of Example 1 was followed except in this instance four doses of 1.0 wt% consisting of a mixture of equal parts by weight of Irganox L57, an alkylated diphenyl amine, and Irganox L109, an alkylated phenol sold by Ciba of Norwich, CT was used the results are shown in Table 2. <tables id="tabl0002" num="0002"><table frame="none"><title><u>TABLE2</u></title><tgroup cols="3" colsep="0"><colspec colnum="1" colname="col1" colwidth="22mm" /><colspec colnum="2" colname="col2" colwidth="33mm" /><colspec colnum="3" colname="col3" colwidth="34mm" /><thead><row><entry align="center" valign="top">Component</entry><entry align="center" valign="top">Concentration, wt%</entry><entry align="center" valign="top">Temperature, °C (°F)</entry></row></thead><tbody><row rowsep="0"><entry>Base Lube</entry><entry align="center">0.00</entry><entry align="center">72.17 (161.9)</entry></row><row rowsep="0"><entry>Antioxidant</entry><entry align="center">1.00</entry><entry align="center">72.56 (162.6)</entry></row><row rowsep="0"><entry>Antioxidant</entry><entry align="center">2.00</entry><entry align="center">72.83 (163.1)</entry></row><row rowsep="0"><entry>Antioxidant</entry><entry align="center">3.00</entry><entry align="center">73.06 (163.5)</entry></row><row rowsep="0"><entry>Antioxidant</entry><entry align="center">4.00</entry><entry align="center">73.67 (164.6)</entry></row></tbody></tgroup></table></tables> As can be seen, increasing amounts of the additive results in increased temperature.
EXAMPLE 3
Two lubricant compositions were tested using the test rig. Each of the compositions tested had a polyalkylene glycol base oil described above. In Composition A (according to the invention) the base oil was a mixture of 93 wt% Dow Synalox 40-D3001 and 5 wt% Dow Synalox 40-D700, each sold by Dow Chemical Company, Houston, TX. The formulation for Composition A is given in Table 3. <tables id="tabl0003" num="0003"><table frame="none"><title><u>TABLE 3</u></title><tgroup cols="3" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="39mm" /><colspec colnum="2" colname="col2" colwidth="30mm" /><colspec colnum="3" colname="col3" colwidth="25mm" /><thead><row><entry valign="top">Component</entry><entry valign="top">Formulation</entry><entry align="center" valign="top">Amount, wt%</entry></row></thead><tbody><row><entry>polyalkylene glycol</entry><entry>Base fluid</entry><entry align="center">98.00</entry></row><row><entry>alkylated diphenyl amine</entry><entry>Antioxidant</entry><entry align="center">0.50</entry></row><row><entry>hindered phenol</entry><entry>Antioxidant</entry><entry align="center">0.50</entry></row><row><entry>N-acylsarcosine</entry><entry>Rust inhibitor</entry><entry align="center">0.15</entry></row><row><entry>Imidazole</entry><entry>Rust inhibitor</entry><entry align="center">0.25</entry></row><row><entry>phenyl phosphorothioate</entry><entry>antiwear additive</entry><entry align="center">0.50</entry></row><row><entry>Tolyltriazole</entry><entry>metal passivator</entry><entry align="center">0.10</entry></row><row><entry>silicone (1%)</entry><entry>Defoamant</entry><entry align="center">0.002</entry></row></tbody></tgroup></table></tables>
Composition B is a commercially available poly alkylene glycol based lubricant.
The results of the test (made in duplicate) are shown graphically in the accompanying figure. As can be seen after equilibrium the composition of the invention, Composition A, had a lower sump operating temperature of 70°C (158°F) when compared to the temperature of 72.2°C (162°F) of the commercially available lube, Composition B.
Contents8
24 sheets
Sheet 1 Sheet 2 Sheet 3 Sheet 4 Sheet 5 Sheet 6 Sheet 7 Sheet 8 Sheet 9 Sheet 10 Sheet 11 Sheet 12 Sheet 13 Sheet 14 Sheet 15 Sheet 16 Sheet 17 Sheet 18 Sheet 19 Sheet 20 Sheet 21 Sheet 22 Sheet 23 Sheet 24
Every citation, both ways
| Document | Relation | Office | Cited during |
|---|---|---|---|
| DE3446646A1 | Cites | Germany | Opposition |
| US5925600A | Cites | United States of America | Opposition |
| DE3446646A1 | Cites | Germany | – |
| EP0460317A | Cites | European Patent Office (EPO) | – |
| EP0667389A | Cites | European Patent Office (EPO) | – |
| US3644482A | Cites | United States of America | – |
| US3663437A | Cites | United States of America | – |
| US4701273A | Cites | United States of America | – |
| US5024677A | Cites | United States of America | – |
| US5925600A | Cites | United States of America | – |
14 priority claims, no other members on record
Priority claims14
| Document | Office | Kind | Date |
|---|---|---|---|
| 544704P | United States of America | – | |
| 54470404 | United States of America | P | |
| 54470404 | United States of America | P | |
| 45755 | United States of America | – | |
| 4575505 | United States of America | A | |
| 4575505 | United States of America | A | |
| 2005004384 | United States of America | W | |
| 2005004384 | United States of America | W | |
| 2005004384 | – | – | – |
| 45755 | – | – | – |
| 544704P | – | – | – |
| US20040544704P | – | – | – |
| US20050045755 | – | – | – |
| WO2005US04384 | – | – | – |
86 legal events, as 8 offices reported them to INPADOC
Over the term
Point at a mark for the eventEvents
| Event | Code | Office | |
|---|---|---|---|
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Application deemed withdrawn, or ip right lapsed, due to non-payment of renewal feeWithdrawnR119 | R119 | DE | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Notification of lapseLapsedST | ST | FR | |
| Gb: european patent ceased through non-payment of renewal feeCeasedGBPC | GBPC | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Fee paymentPLFP | PLFP | FR | |
| Patent maintained in amended form27A | 27A | EP | |
| Designated contracting statesAK | AK | EP | |
| Epo decision maintaining patent in amended form now finalR102 | R102 | DE | |
| Patent maintained in amended formORIGINAL CODE: 0009272PUAH | PUAH | EP | |
| Information on the status of an ep patent application or granted ep patentGrantedSTATUS: PATENT MAINTAINED AS AMENDEDSTAA | STAA | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Information provided on ipc code assigned after grantRIC2 | RIC2 | EP | |
| Fee paymentPLFP | PLFP | FR | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Reply of patent proprietor to notice(s) of opposition receivedOppositionORIGINAL CODE: EPIDOSNOBS3PLBB | PLBB | EP | |
| Patent lapsedLapsedMM4A | MM4A | IE | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Patent ceasedCeasedPL | PL | CH | |
| Opposition filed against patentOppositionR026 | R026 | DE | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Opposition filedOpposition26 | 26 | EP | |
| Notice of opposition and request to file observation + time limit sentOppositionORIGINAL CODE: EPIDOSNOBS2PLAX | PLAX | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Opposition filedOppositionORIGINAL CODE: 0009260PLBI | PLBI | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Deletion acc. to par. 5 (withdrawal of the translation of the ep patent)MK05 | MK05 | AT | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lt: invalidation of european patent or patent extensionLTIE | LTIE | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Discontinued in the netherlands as no translation has been filedVDEP | VDEP | NL | |
| Dpma publication of mentioned ep patent grantGrantedR096 | R096 | DE | |
| European patents granted designating irelandGrantedFG4D | FG4D | IE | |
| European patent takes effect as a national patent in ch/liEP | EP | CH | |
| Designated contracting statesAK | AK | EP | |
| European patent grantedGrantedFG4D | FG4D | GB | |
| (expected) grantORIGINAL CODE: 0009210GRAA | GRAA | EP | |
| Grant fee paidORIGINAL CODE: EPIDOSNIGR3GRAS | GRAS | EP | |
| Title (correction)HIGH EFFICIENCY POLYALKYLENE GLYCOL LUBRICANTS FOR USE IN WORM GEARSRTI1 | RTI1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Information provided on ipc code assigned before grantRIC1 | RIC1 | EP | |
| Title (correction)HIGH EFFICIENCY POLYALKYLENE GLYCOL LUBRICANTS FOR USE IN WORM GEARSRTI1 | RTI1 | EP | |
| Despatch of communication of intention to grant a patentORIGINAL CODE: EPIDOSNIGR1GRAP | GRAP | EP | |
| Request for extension of the european patent (deleted)DAX | DAX | EP | |
| Request for examination filed17P | 17P | EP | |
| Designated contracting statesAK | AK | EP | |
| Public reference made under article 153(3) epc to a published international application that has entered the european phaseORIGINAL CODE: 0009012PUAI | PUAI | EP |
Numbers
- Publication
- 1733010
- Publication, DOCDB
- 1733010
- Publication, EPODOC
- EP1733010
- Application
- 57133662
- Application, DOCDB
- 05713366
- Application, EPODOC
- EP20050713366
Titles3
- German
- Hochwirksame Polyalkylenglykol-Schmiermittel zur Verwendung in Schneckengetrieben
- English
- High efficiency polyalkylene glycol lubricants for use in worm gears
- French
- Lubrifiants de haute performance à base de polyalkyleneglycol utilisés dans des vis sans fin
Classification
- CPC, 23
- C10M169/04
- C10M2207/283
- C10M2209/1033
- C10M2209/1045
- C10M2209/1055
- C10M2215/064
- C10M2215/08
- C10M2215/223
- C10M2215/224
- C10M2223/047
- C10M2229/02
- C10N2220/022
- C10N2020/02
- C10N2230/40
- C10N2030/40
- C10N2230/62
- C10N2030/62
- C10N2240/02
- C10N2040/02
- C10N2040/04
- C10N2240/04
- C10N2240/30
- C10N2040/30
- IPC, 12
- C10M169 04
- C10N20 02
- C10N30 06
- C10N30 10
- C10N30 12
- C10N30 14
- C10N40 04
- C10M107 34
- C10M129 76
- C10M133 12
- C10M133 16
- C10M133 46
Designated states30
- Contracting states, 30
- Austria
- Belgium
- Bulgaria
- Switzerland
- Cyprus
- Czechia
- Germany
- Denmark
- Estonia
- Spain
- Finland
- France
- United Kingdom
- Greece
- Hungary
- Ireland
- Iceland
- Italy
- Liechtenstein
- Lithuania
- Luxembourg
- Monaco
- Netherlands (Kingdom of the)
- Poland
and 6 moreShow fewer
- Portugal
- Romania
- Sweden
- Slovenia
- Slovakia
- Türkiye