Lubricant composition and use as a lubricant additive of guanidinium-based ionic liquids
Use of a guanidinium-based ionic liquid as detergent in a lubricant composition, notably for lubricating marine engines. A lubricant composition including a guanidinium-based ionic liquid.
1. 1 . A method for reducing and/or limiting and/or preventing and/or delaying the formation of deposits or for reducing the deposits already present on internal parts of a marine combustion engine comprising applying a guanidinium-based ionic liquid or a lubricant composition comprising the guanidinium-based ionic liquid to the internal parts of the marine combustion engine,
wherein the guanidinium-based ionic liquid corresponds to formula (I):
[CAT + ][X − ] (I)
wherein
[X − ] represents one or more anionic species, [CAT + ] is selected from cations of formula (II):
wherein:
R1, R2 are each independently selected from H, a C1-C30 linear or branched alkyl group, a C3-C8 cycloalkyl group, a C6-C12 aryl group, or a C7-C12 aralkyl group, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom,
R3, R4, R5, R6 are each independently selected from a C1-C30 linear or branched alkyl group, a C3-C8 cycloalkyl group, a C6-C12 aryl group, or a C7-C12 aralkyl group, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom,
or any two of (R3, R4) or (R5, R6) form together a methylene chain —(CH2)p-, with p is an integer from 2 to 5.
2. The method according to claim 1 , wherein the guanidinium-based ionic liquid or the lubricant composition is applied to the cylinder wall of the marine combustion ,engine.
3. The method according to claim 1 , wherein in formula (II):
R1, R2 are each independently selected from H, a C1-C6 linear or branched alkyl group,
R3, R4, R5, R6 are each independently selected from a C1-C6 linear or branched alkyl group.
4. The method according to claim 3 , wherein in formula (II):
R1, R2 are independently selected from the group consisting of H, methyl group and ethyl group,
R3, R4, R5, R6 are independently selected from methyl group and ethyl group.
5. The method according to claim 4 , wherein [CAT + ] is selected from:
6. The method according to claim 1 , wherein [X − ] represents one or more anions selected from the group consisting of carboxylates, hydroxycarboxylates and alcoholates.
7. The method according to claim 6 , wherein [X − ] is selected from:
a) carboxylates Ra—COO − , wherein Ra is selected from alkyl and alkenyl groups comprising from 1 to 30 atoms of carbon, aryl groups comprising from 6 to 30 atoms of carbon, aralkyl groups comprising from 7 to 30 atoms of carbon, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom;
b) alcoholates RaRbHCO − , wherein Ra is selected from alkyl and alkenyl groups comprising from 1 to 30 atoms of carbon, aryl groups comprising from 6 to 30 atoms of carbon, aralkyl groups comprising from 7 to 30 atoms of carbon, Rb is selected from H, alkyl and alkenyl groups comprising from 1 to 30 atoms of carbon, aryl groups comprising from 6 to 30 atoms of carbon, aralkyl groups comprising from 7 to 30 atoms of carbon, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom;
c) hydroxycarboxylates HO-Rc-COO − , wherein Rc is a di-radical selected from alkyl and alkenyl groups comprising from 1 to 30 atoms of carbon, aryl groups comprising from 6 to 30 atoms of carbon, aralkyl groups comprising from 7 to 30 atoms of carbon, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom.
8. The method according to claim 7 , wherein [X − ] is selected from the group consisting of 2-ethylhexanoate, 2-hydroxypropanoate, tert-amylphenolate and isooctylphenolate.
9. A method for lubricating two-stroke marine engines and four-stroke marine engines, said method comprising applying a marine lubricant composition to internal parts of said marine engine, where said marine lubricant composition comprising:
from 30.0 to 94% of at least one base oil,
from 0.05 to 15.0% of at least one guanidinium-based ionic liquid,
at least one detergent selected from neutral and overbased detergents having a Total Base Number according to ASTM D2896 of from 20 to 450 mg KOH/g
the percentages being defined by weight of component as compared to the total weight of the composition
wherein the guanidinium-based ionic liquid responds to formula (I):
[CAT + ][X − ] (I)
wherein
[X − ] represents one or more anionic species, [CAT + ] is selected from cations of formula (II):
wherein:
R1, R2 are each independently selected from H, a C1-C30 linear or branched alkyl group, a C3-C8 cycloalkyl group, a C6-C12 aryl group, or a C7-C12 aralkyl group, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom,
R3, R4, R5, R6, are each independently selected from a C1-C30 linear or branched alkyl group, a C3-C8 cycloalkyl group, a C6-C12 aryl group, or a C7-C12 aralkyl group, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom,
or any two of (R3, R4) or (R5, R6) form together a methylene chain —(CH2)p-, with p is an integer from 2 to 5.
10. The method of claim 9 wherein the marine lubricant composition comprises from 1 to 35% weight of neutral and overbased detergents, with regards to the total weight of the lubricant composition.
11. The method according to claim 9 , wherein the percentage by weight of guanidinium-based ionic liquid relative to the total weight of lubricant composition is chosen such that the alternative BN provided by the oil-soluble guanidinium-based ionic liquid represents at least 3% of the BN of said lubricant composition.
12. The method according to claims 9 , wherein the marine lubricant composition has a Total Base Number (TBN) value according to ASTM D2896 of above 10 mg KOH/g.
13. The method according to claim 9 , wherein the marine lubricant composition has a kinematic viscosity at 100° C. superior or equal to 5.6 mm 2/s and inferior or equal to 21.9 mm 2/s.
14. The method according to claim 9 , wherein [CAT + ] is selected from:
15. The method according to claim 9 , wherein [X − ] is selected from:
a) carboxylates Ra—COO − , wherein Ra is selected from alkyl and alkenyl groups comprising from 1 to 30 atoms of carbon, aryl groups comprising from 6 to 30 atoms of carbon, aralkyl groups comprising from 7 to 30 atoms of carbon, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom;
b) alcoholates RaRbHCO − , wherein Ra is selected from alkyl and alkenyl groups comprising from 1 to 30 atoms of carbon, aryl groups comprising from 6 to 30 atoms of carbon, aralkyl groups comprising from 7 to 30 atoms of carbon, Rb is selected from H, alkyl and alkenyl groups comprising from 1 to 30 atoms of carbon, aryl groups comprising from 6 to 30 atoms of carbon, aralkyl groups comprising from 7 to 30 atoms of carbon, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom;
c) hydroxycarboxylates HO-Rc-COO − , wherein Rc is a di-radical selected from alkyl and alkenyl groups comprising from 1 to 30 atoms of carbon, aryl groups comprising from 6 to 30 atoms of carbon, aralkyl groups comprising from 7 to 30 atoms of carbon, optionally substituted by a functional group comprising an oxygen and/or a nitrogen atom.