Patent Grant
8530686
The invention relates to novel organic molybdenum compounds, the use thereof as friction-modifiers and lubricating compositions which contain said compounds.
Friction-modifiers (friction-adjusting agents) are used for adjusting the friction characteristics of a lubricant to an appropriate level. Friction-modifiers which reduce friction are used in lubricating compositions such as gear oils and engine oils with a view to reducing fuel costs. Friction-modifiers which raise friction are used for maintaining a certain high friction level in the lubricating compositions which are used in the wet-type clutch part of an automatic gear box. Many types of such friction-modifiers have been proposed.
The organic molybdenum compounds are the most typical of these friction-modifiers and, as shown in “Shinban Sekiyu Seihin Tenkasai” (New Edition, Additives for Petroleum Products), by Toshio SAKURAI, Saiwai Shobo Co., published 25 Jul. 1986, these organic molybdenum compounds are compounds which have two molybdenum atoms in one molecule as shown in formulae (2) and (3) below.
(Those compounds for which in this formulae x=0 and y=4, and for which x+y=4, and for which x≧2 are insoluble in oil and the others are oil-soluble.)
Furthermore, compounds in which the element molybdenum is included twice in one molecule have been disclosed in Japanese Patent No. 3495764, Japanese Examined Patent Publication 45-24562, Japanese Unexamined Patent Application Laid Open 52-19629, Japanese Unexamined Patent Application Laid Open 52-106824, and Japanese Unexamined Patent Application Laid Open 48-56202.
A problem with catalyst poisoning in the apparatus which is used for cleaning-up the exhaust gas arises when compounds which contain phosphorus in the molecule as shown in the aforementioned general formula (2) are added to engine oils and there is a demand for compounds which are phosphorus-free.
An object of the present invention is to provide novel compounds which are useful as lubricating additives and the like which do not contain phosphorus, which reduce the friction coefficient and control the friction of a wet-type clutch, for example, optimally, and friction modifiers comprising said compounds.
A further object of the invention is to provide lubricating compositions which contain these compounds.
To achieve these objects, the present invention provides dicyclopentadienyl molybdenum crosslinked complexes having general formula (1) below.
In this formula X is the element oxygen or the element sulphur, Y is the element oxygen or Y is absent, and R1 to R10 are groups selected individually from the group comprising hydrogen, a methyl group and an ethyl group.
According to a preferred embodiment the dicyclopentadienyl molybdenum crosslinked complexes of general formula (1) can be represented by general formula (2) which is indicated below.
In this formula R1 to R10 are groups selected individually from the group comprising hydrogen, a methyl group and an ethyl group.
According to a preferred embodiment the dicyclopentadienyl molybdenum crosslinked complexes of general formula (1) can be represented by general formula (3) which is indicated below.
In this formula R1 to R10 are groups selected individually from the group comprising hydrogen, a methyl group and an ethyl group.
According to a preferred embodiment the dicyclopentadienyl molybdenum crosslinked complexes of general formula (1) can be represented by general formula (4) which is indicated below.
In this
formula R1 to R10 are groups selected individually from the group comprising hydrogen, a methyl group and an ethyl group.
According to a preferred embodiment the dicyclopentadienyl molybdenum crosslinked complexes of general formula (1) can be represented by general formula (5) which is indicated below.
In this formula R1 to R10 are groups selected individually from the group comprising hydrogen, a methyl group and an ethyl group.
Further the present invention provides the use of the dicyclopentadienyl molybdenum crosslinked complexes as friction-modifiers.
Also the present invention provides lubricating compositions which contain the compounds.
The compounds of this invention can be produced, for example, using the method indicated below.
First Process
Synthesis of the Synthesis Intermediate Raw Material Dicyclopentadienyl Molybdenum Hexa-Carbonyl Complex
Second Process
Synthesis of the Dicyclopentadienyl Molybdenum Crosslinked Complex
The di(cyclopentadienyl) μ-thioxomolybdenum complex of general formula (2), the di(cyclopentadienyl) μ-thioxodioxomolybdenum complex of general formula (3), the di(cyclopentadienyl) μ-oxomolybdenum complex of general formula (4) and the di(cyclopentadienyl) μ-oxodioxomolybdenum complex of general formula (5) are produced simultaneously in accordance with the reaction equation indicated below.
Hydrogen, the methyl group and the ethyl group can be cited for the aforementioned R1 to R10, and the compounds with combinations such as those shown in Tables 1 to 18 below can be cited.
Lubricating oils and greases, for example, can be cited as lubricating compositions of this invention. The amount of a compound of this invention in a lubricating composition is the same as with the conventional friction-modifiers, for example, being compounded in a proportion with respect to the composition generally of some 0.1 to 10 wt %.
There are no particular limitations regarding the base oil or grease used in lubricating composition according to the present invention, and various conventional greases, mineral oils and synthetic oils may be conveniently used. For the purpose of this description, the term “base oil” is meant to also include a grease base stock.
The base oil used in the present invention may conveniently comprise mixtures of one or more mineral oils and/or one or more synthetic oils.
Mineral oils include liquid petroleum oils and solvent-treated or acid-treated mineral lubricating oil of the paraffinic, naphthenic, or mixed paraffinic/naphthenic type which may be further refined by hydrofinishing processes and/or dewaxing.
Suitable base oils for use in the lubricating oil composition of the present invention are Group I, Group II or Group III base oils, polyalphaolefins, Fischer-Tropsch derived base oils and mixtures thereof.
By “Group I” base oil, “Group II” base oil and “Group III” base oil in the present invention are meant lubricating oil base oils according to the definitions of American Petroleum Institute (API) categories I, II and III. Such API categories are defined in API Publication 1509, 15th Edition, Appendix E, April 2002.
Suitable Fischer-Tropsch derived base oils that may be conveniently used as the base oil in the lubricating oil composition of the present invention are those as for example disclosed in EP 0 776 959, EP 0 668 342, WO 97/21788, WO 00/15736, WO 00/14188, WO 00/14187, WO 00/14183, WO 00/14179, WO 00/08115, WO 99/41332, EP 1 029 029, WO 01/18156 and WO 01/57166.
Synthetic oils include hydrocarbon oils such as olefin oligomers (PAOs), dibasic acid esters, polyol esters, and dewaxed waxy raffinate. Synthetic hydrocarbon base oils sold by the Shell Group under the designation “XHVI” (trade mark) may be conveniently used.
(1) Novel phosphorus-free Mo-based friction-modifiers have been obtained.
(2) The compounds of this invention exhibit a low friction coefficient and they can be used in particular as friction modifiers for various types of energy-saving engine lubricating oils.
(3) The compounds of this invention are especially suitable for use as friction-modifiers for fuel-saving engine oils as they are phosphorus-free.
(4) There is no damage to the catalysts (removal of NOx) which are housed in automobile exhaust gas cleaning apparatus.
The invention is described below by means of Examples and Comparative Examples but the invention is not limited in any way by these examples.
The synthesis of Compound 6 in the aforementioned Table 1, the case where X is S, there is no Y and R1 to R10 are CH3.
(i) First Process
Tetrahydrofuran (THF, 45 ml) was added to 3.75 g (18.8 mmol) of pentamethylcyclopentadiene and, after being cooled to −78° C., 12.5 ml (18.8 mmol) of Bu-Li were added dropwise and lithium pentamethylcyclopentadienyl was co-ordinated. Then 5 g (18.8 mmol) of molybdenum hexa-carbonyl were added to this material and heated under reflux for 48 hours and, after the reaction had been completed, the mother liquor was cooled to 0° C. Separately, 3.2 g (18.8 mmol) of iron(II) sulphate was added to a solution comprising a mixture of 100 ml of pure water and 20 ml of acetic acid and the solution so obtained was added dropwise to the mother liquor. The red coloured solution obtained was subjected to suction filtration, washed and dried and the di(pentamethylcyclopentadienyl)molybdenum hexa-carbonyl complex was obtained by recrystallization. Yield 24%
(ii) Second Process
The di(pentamethylcyclopentadienyl)molybdenum hexa-carbonyl complex (0.5 g, 0.79 mmol) and 0.69 g (5.84 mmol) of 3-sulphorane were dissolved in 100 ml of toluene and heated under reflux at 120° C. for 3 hours. After the reaction had been completed the solvent was removed and the reaction product was subjected to column chromatography and a red coloured complex was isolated. Yield 3%
The synthesis of Compound 5 in the aforementioned Table 1, the case where X is S, Y is O and R1 to R10 are CH3.
The aforementioned di(heptamethylcyclopentadienyl)molybdenum hexa-carbonyl complex (0.5 g, 0.79 mmol) and 0.69 g (5.84 mmol) of 3-sulphorane were dissolved in 100 ml of toluene and heated under reflux at 120° C. for 3 hours. After the reaction had been completed the solvent was removed and the reaction product was subjected to column chromatography and an orange coloured complex was isolated. Yield 4%
The synthesis of Compound 3 in the aforementioned Table 1, the case where X and Y are O and R1 to R10 are H.
(i) First Process
Tetrahydrofuran (THF, 45 ml) was added to 18.8 mmol of cyclopentadiene and, after being cooled to −78° C., 12.5 ml (18.8 mmol) of Bu-Li were added dropwise and the lithium pentamethylcyclopentadienyl was co-ordinated. Then 5 g (18.8 mmol) of molybdenum hexa-carbonyl were added to this material and heated under reflux for 48 hours and, after the reaction had been completed, the mother liquor was cooled to 0° C. Separately, 3.2 g (18.8 mmol) of iron(II) sulphate was added to a solution comprising a mixture of 100 ml of pure water and 20 ml of acetic acid and the solution so obtained was added dropwise to the mother liquor. The red coloured solution obtained was subjected to suction filtration, washed and dried and the di(cyclo-pentadienyl)molybdenum hexa-carbonyl complex was obtained by recrystallization. Yield 20%
(ii) Second Process
The di(cyclopentadienyl)molybdenum hexa-carbonyl complex (0.5 g, 1.02 mmol) and 0.6 g (5.08 mmol) of 3-sulphorane were dissolved in 50 ml of toluene and heated under reflux at 120° C. for 3 hours. After removing the solvent the yellow coloured product di(cyclopentadienyl) μ-oxodioxomolybdenum complex was produced and isolated from the reaction mixture by means of column chromatography. Yield 34%
The synthesis of Compound I in the aforementioned Table 1, the case where X is S, Y is O and R1 to R10 are H.
Reaction in the same way as in Example 3 and the red coloured product di(cyclopentadienyl) μ-thioxodioxomolybdenum complex was isolated by means of column chromatography. Yield 14%
The complex obtained in Example 2 was adjusted in such a way as to provide an Mo content of 500 ppm in engine oil (di-isononyl adipic acid) (viscosity at 100° C.: 3.04 mm2/s) to which 5% of a dispersing agent (alkenylsuccinic acid polyalkylene polyimide, trade name Infineum C9266) had been added.
The case where the complex obtained in Example 2 had not been used in the composition of Example 5 was taken as Comparative Example 1. Both of the compositions are shown in Table 20 below.
These sample oils were subjected to 30 minute friction coefficient measurement and evaluation under the conditions shown in Table 19 below using an SRV tester (a reciprocating movement tester of the cylinder-on-disc type shown in
Testing Conditions
The case of the Example 5 exhibited a low friction coefficient when compared with the base oil with no addition (Comparative Example 1) from 1 minute after the start of the test and it is clear that the compound had the function of a friction-modifier. That is to say, the compounding of a friction-modifier of this invention clearly shows a lower friction coefficient when compared with the case where it has not been compounded.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2007-023479 | Feb 2007 | JP | national |
The present application is a continuation of U.S. Ser. No. 12/525,359, filed on Nov. 25, 2009, which claims priority from PCT/US2008/051258, filed Feb. 1, 2008, which claims priority from JP 2007-023479, filed Feb. 1, 2007, all of which are incorporated herein by reference.
| Number | Name | Date | Kind |
|---|---|---|---|
| 3069445 | Gorsich | Dec 1962 | A |
| 3272606 | Brown et al. | Sep 1966 | A |
| 4966719 | Coyle et al. | Oct 1990 | A |
| 5126465 | Greaney et al. | Jun 1992 | A |
| Number | Date | Country |
|---|---|---|
| 3717143 | Dec 1988 | DE |
| 0668342 | Aug 1995 | EP |
| 0776959 | Jun 1997 | EP |
| 1029029 | Aug 2000 | EP |
| 1741772 | Oct 2007 | EP |
| 789383 | Jan 1958 | GB |
| 48056202 | Aug 1973 | JP |
| 52019629 | Feb 1977 | JP |
| 52106824 | Sep 1977 | JP |
| 62161992 | Jul 1987 | JP |
| 3495764 | Feb 2004 | JP |
| WO9721788 | Jun 1997 | WO |
| WO9941332 | Aug 1999 | WO |
| WO0008115 | Feb 2000 | WO |
| WO0014179 | Mar 2000 | WO |
| WO0014183 | Mar 2000 | WO |
| WO0014187 | Mar 2000 | WO |
| WO0014188 | Mar 2000 | WO |
| WO0015736 | Mar 2000 | WO |
| WO0118156 | Mar 2001 | WO |
| WO0157166 | Aug 2001 | WO |
| Entry |
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| Number | Date | Country | |
|---|---|---|---|
| 20130060055 A1 | Mar 2013 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12525359 | US | |
| Child | 13665714 | US |
