Molybdenum compounds
View Patent ↗Novel molybdenum compounds are prepared by reacting a hindered amine with a molybdenum source, in the presence of one of (a) water, (b) a diol and water, and (c) the reaction product of a fatty oil and a multifunctional amine, and water. Lubricant compositions containing these new compounds are more stabilized against oxidation and have improved friction reducing properties. Synergy is observed when the novel compounds are combined with a diaryl amine in a lubricant composition.
1. A novel molybdenum compound which is a reaction product of a hindered amine and a molybdenum source, and one of the following:
(a) the reaction product of a fatty oil with a diethanolamine and water; or
(b) a diol and water, wherein the diol is of the following formula:
where n=0 to 12, and R 33 and R 34 is hydrogen or a hydrocarbon with between 1 and 25 carbon atoms,
wherein the hindered amine is one or more chosen from the group consisting of:
(a) a compound of the formula
where R 16 is H, O or a hydrocarbon from 1 to 25 carbon atoms, an alkoxy radical with the oxygen bound to the nitrogen with the alkyl portion containing 1 to 25 carbon atoms, or a COR group, the R begin a hydrocarbon containing from 1 to 25 carbon atoms, R 17 , R 18 , R 22 , R 23 are hydrocarbons with 1 to 25 carbon atoms, R 19 , R 21 are H or hydrocarbons with 1 to 25 carbon atoms,
when n=1, R 20 is OH, H, O, NH 2 , NR 2 where R is a hydrocarbon with 1 to 25 carbon atoms, an ester group O 2 CR where R is a hydrocarbon with 1 to 25 carbon atoms, or a succinimide group,
when n=2, R 20 is the diacyl radical of an aliphatic dicarboxylic acid having 4 to 12 carbon atoms
(b) 4-stearoyloxy-2,2,6,6-tetramethylpiperidine,
(c) di(2,2,6,6-tetramethylpiperidin-4-yl)sebacate,
(d) di(1,2,2,6,6-pentamethylpiperidin-4-yl)sebacate,
(e) bis(1-octyloxy-2,2,6,-tetramethyl-4-piperidyl)sebacate
(f) polymer-bound piperidine compound,
(g) a compound of the group consisting of 2,2,6,6-tetramethylpiperidines, 1,2,2,6,6-pentamethylpiperidines, 1-oxo-2,2,6,6-tetramethylpiperidines, and 1-alkoxy-2,2,6,6-tetramethylpiperidines, and
(h) a compound of the group consisting of di(1,2,2,6,6-pentamethylpiperidin-4-yl)sebacate, 4-stearoyloxy-2,2,6,6-tetramethylpiperidine, di(,2,2,6,6-tetramethylpiperidin-4-yl)sebacate and bis (1-octyloxy-2,2,6,-tetramethyl-4-piperidyl)sebacate.
2. The novel molybdenum compound according to claim 1 , wherein the diol is 2-ethyl-1,3-hexanediol or 1,2-dodecanediol.
3. The novel molybdenum compound according to claim 1 , wherein the molybdenum source is one of a metal salt of molybdic acid, ammonium molybdate, and molybdenum trioxide.
4. A lubricating composition, comprising at least 50 wt % of a lubricating oil basestock and a molybdenum compound, the molybdenum compound being a reaction product of a hindered amine and a molybdenum source and one of the following:
(a) the reaction product of a fatty oil with a diethanolamine, and water, or
(b) a diol, and water, wherein the diol is of the following formula:
where n=0 to 12, and R 33 and R 34 is hydrogen or a hydrocarbon with between 1 and 25 carbon atoms,
wherein the molybdenum compound is present in the lubricating composition in an amount which provides 1 to 2000 ppm molybdenum, and
wherein the hindered amine is one or more chosen from the group consisting of:
(a) a compound of the formula
where R 16 is H, O or a hydrocarbon from 1 to 25 carbon atoms, an alkoxy radical with the oxygen bound to the nitrogen with the alkyl portion containing 1 to 25 carbon atoms, or a COR group, the R being a hydrocarbon containing from 1 to 25 carbon atoms, R 17 , R 18 , R 22 , R 23 are hydrocarbons with 1 to 25 carbon atoms, R 19 , R 21 are H or hydrocarbons with 1 to 25 carbon atoms,
when n=1, R 20 is OH, H, O, NH 2 , NR 2 where R is a hydrocarbon with 1 to 25 carbon atoms, an ester group O 2 CR where R is a hydrocarbon with 1 to 25 carbon atoms, or a succinimide group,
when n=2, R 20 is the diacyl radical of an aliphatic dicarboxylic acid having 4 to 12 carbon atoms
(b) 4-stearoyloxy-2,2,6,6-tetramethylpiperidin,
(c) di(2,2,6,6-tetramethylpiperidin-4-yl)sebacate,
(d) di(1,2,2,6,6-pentamethylpiperidin-4-yl)sebacate,
(e) bis(1-octyloxy-2,2,6,-tetramethyl-4-piperidyl)sebacate
(f) polymer-bound piperidine compound,
(g) a compound of the group consisting of 2,2,6,6-tetramethylpiperidines, 1,2,2,6,6-pentamethylpiperidines, 1-oxo-2,2,6,6-tetramethylpiperidines, and 1-alkoxy-2,2,6,6-tetramethylpiperidines, and
(h) a compound of the group consisting of di(1,2,2,6,6-pentamethylpiperidin-4-yl)sebacate, 4-stearoyloxy-2,2,6,6-tetramethylpiperidine, di(,2,2,6,6-tetramethylpiperidin-4-yl)sebacate and bis (1-octyloxy-2,2,6,-tetramethyl-4-piperidyl)sebacate.
5. The lubricating composition of claim 4 , wherein the molybdenum compound is present in the lubricating composition in an amount which provides about 50 to 750 ppm molybdenum.
6. The lubricating composition of claim 5 , wherein the molybdenum compound is present in the lubricating composition in an amount which provides about 125 to 750 ppm molybdenum.
7. The lubricating composition of claim 4 , wherein the molybdenum compound is present in the lubricating composition in an amount which provides about 700 ppm molybdenum.
8. The lubricating composition of claim 4 , further comprising a diaryl amine in an amount sufficient to provide about 0.001 to 2 wt % diarlyamine in the lubricating composition.
9. The lubricating composition of claim 4 , wherein the diaryl amine in an amount sufficient to provide about 0.5 to 1.5 wt % diarlyamine in the lubricating composition.
10. A process for preparing a novel molybdenum compound, comprising the steps of combining in a reaction vessel (1) a molybdenum source, (2) a hindered amine, and one of (3) (i) a diol and water, and (ii) the reaction of product of a fatty oil and a diethanolamine, and water; heating the reactants to a temperature between 60 and 150° C. for a period of 1 to 6 hours; and removing the water,
wherein the diol is of the following formula:
where n=0 to 12, and R 33 and R 34 is hydrogen or a hydrocarbon with between 1 and 25 carbon atoms, and
wherein the hindered amine is one or more chosen from the group consisting of:
(a) a compound of the formula
where R 16 is H, O or a hydrocarbon from 1 to 25 carbon atoms, an alkoxy radical with the oxygen bound to the nitrogen with the alkyl portion containing 1 to 25 carbon atoms, or a COR group, the R being a hydrocarbon containing from 1 to 25 carbon atoms, R 17 , R 18 , R 22 , R 23 are hydrocarbons with 1 to 25 carbon atoms, R 19 , R 21 are H or hydrocarbons with 1 to 25 carbon atoms,
when n=1, R 20 is OH, H, O, NH 2 , NR 2 where R is a hydrocarbon with 1 to 25 carbon atoms, an ester group O 2 CR where R is a hydrocarbon with 1 to 25 carbon atoms, or a succinimide group,
when n=2, R 20 is the diacyl radical of an aliphatic dicarboxylic acid having 4 to 12 carbon atoms
(b) 4-stearoyloxy-2,2,6,6-tetramethylpiperidine,
(c) di(2,2,6,6-tetramethylpiperidin-4-yl)sebacate,
(d) di(1,2,2,6,6-pentamethylpiperidin-4-yl)sebacate,
(e) bis(1-octyloxy-2,2,6,-tetramethyl-4-piperidyl)sebacate
(f) polymer-bound piperidine compound
(g) a compound of the group consisting of 2,2,6,6-tetramethylpiperidines, 1,2,2,6,6-pentamethylpiperidines, 1-oxo-2,2,6,6-tetramethylpiperidines, and 1-alkoxy-2,2,6,6-tetramethylpiperidines, and
(h) a compound of the group consisting of di(1,2,2,6,6-pentamethylpiperidin-4-yl)sebacate, 4-stearoyloxy-2,2,6,6-tetramethylpiperidine, di(,2,2,6,6-tetramethylpiperidin-4-yl)sebacate and bis (1-octyloxy-2,2,6,-tetramethyl-4-piperidyl)sebaca.