[0001] The present invention relates to a lubricating composition, in particular for use
as a gas engine oil.
[0002] In recent years the specifications for finished lubricants have required the lubricant
formulators to develop lubricants having, among others, improved friction reducing
properties with the purpose of meeting energy saving (or "fuel economy") trends.
[0003] As an example,
US 2007/0265176 discloses to this end the use of a lubricating oil composition comprising a major
amount of a base oil having a viscosity index greater than 80, a kinematic viscosity
at 100°C of from 2 to 50 mm
2/s, containing 90 wt.% or more saturates, having less than 5 ppm sulphur and wherein
the base oil is derived from a waxy feed, and a minor amount of: (a) a polyol ester
of an aliphatic carboxylic acid having 12 to 24 carbon atoms; and (b) an oil soluble
or oil dispersible molybdenum compound.
[0004] Furthermore,
US 2008/0015127 discloses the use of a lubricating composition comprising a base oil, a friction
modifier and a dispersant wherein the lubricating composition comprises less than
325 ppm boron.
[0005] US 6 562 765 discloses an engine oil comprising a base oil and at least 450 ppm molybdenum of
a friction modifier composition containing a specific oxymolybdenum complex and a
specific molybdenum dithiocarbamate.
[0006] It is an object of the present invention to improve the friction reduction properties
of lubricating compositions, especially for use in a gas engine.
[0007] It is another object of the present invention to provide alternative lubricating
compositions for use in a gas engine.
[0008] One or more of the above or other objects can be obtained by the present invention
by providing a lubricating composition comprising:
- a base oil;
- a molybdenum-containing compound; and
- a fatty acid amides.
[0009] It has now surprisingly been found according to the present invention that the lubricating
compositions according to the present invention may exhibit improved friction reduction
properties.
[0010] There are no particular limitations regarding the base oil used in lubricating composition
according to the present invention, and various conventional mineral oils, synthetic
oils as well as naturally derived esters such as vegetable oils may be conveniently
used.
[0011] 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; thus, according to the
present invention, the term "base oil" may refer to a mixture containing more than
one base oil. 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.
[0012] Suitable base oils for use in the lubricating oil composition of the present invention
are Group I-III mineral base oils, Group IV poly-alpha olefins (PAOs), Group I-III
Fischer-Tropsch derived base oils and mixtures thereof.
[0013] By "Group I", "Group II", "Group III" and "Group IV" base oils in the present invention
are meant lubricating oil base oils according to the definitions of American Petroleum
Institute (API) for category III and IV. These API categories are defined in
API Publication 1509, 15th Edition, Appendix E, April 2002.
[0014] Fischer-Tropsch derived base oils are known in the art. By the term "Fischer-Tropsch
derived" is meant that a base oil is, or is derived from, a synthesis product of a
Fischer-Tropsch process. A Fischer-Tropsch derived base oil may also be referred to
as a GTL (Gas-To-Liquids) base oil. Suitable Fischer-Tropsch derived base oils that
may be conveniently used as the base oil in the lubricating 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.
[0015] Synthetic oils include hydrocarbon oils such as olefin oligomers (including polyalphaolefin
base oils; PAOs), dibasic acid esters, polyol esters, polyalkylene glycols (PAGs),
alkyl naphthalenes and dewaxed waxy isomerates. Synthetic hydrocarbon base oils sold
by the Shell Group under the designation "Shell XHVI" (trade mark) may be conveniently
used.
[0016] Poly-alpha olefin base oils (PAOs) and their manufacture are well known in the art.
Preferred poly-alpha olefin base oils that may be used in the lubricating compositions
of the present invention may be derived from linear C
2 to C
32, preferably C
6 to C
16, alpha olefins. Particularly preferred feedstocks for said poly-alpha olefins are
1-octene, 1-decene, 1-dodecene and 1-tetradecene.
[0017] The total amount of base oil incorporated in the lubricating composition of the present
invention is preferably present in an amount in the range of from 60 to 99 wt.%, more
preferably in an amount in the range of from 65 to 98 wt.% and most preferably in
an amount in the range of from 70 to 95 wt.%, with respect to the total weight of
the lubricating composition.
[0018] There are no particular limitations regarding the molybdenum-containing compound
used in lubricating composition according to the present invention and various conventional
molybdenum-containing compounds may be conveniently used.
[0019] Preferably, the molybdenum-containing compound is a sulphur-containing molybdenum-containing
compound such as a compound selected from the group consisting of a molybdenum dithiocarbamate
(MoDTC), molybdenum dithiophosphate, molybdenum dithiophosphinate, molybdenum xanthate,
molybdenum thioxanthate, molybdenum sulfide and mixtures thereof. The molybdenum-containing
compound may also be a di- or trinuclear molybdenum compound. Most preferably, the
molybdenum compound is a molybdenum dithiocarbamate compound. Preferably the lubricating
composition according to the present invention comprises at least 0.40 wt.%, more
preferably at least 0.45 wt.%, even more preferably at least 0.50 wt.% of the molybdenum-containing
compound, based on the total weight of the lubricating composition. Typically, the
lubricating composition comprises at most 1.5 wt.%, more typically at most 1.0 wt.%,
of the molybdenum-containing compound, based on the total weight of the lubricating
composition.
[0020] There are no particular limitations regarding the fatty acid amide as used in lubricating
composition according to the present invention and various conventional saturated
or unsaturated fatty acid amides such as oleamide, stearamide, behenamide, docosamide,
erucamide may be conveniently used. Preferably the fatty acid amide contains from
12 to 26 carbon atoms, more preferably from 16 to 24 carbon atoms, most preferably
from 18 to 22 carbon atoms. Especially preferred are the unsaturated fatty acid amides,
preferably containing 18 to 22 carbon atoms such as oleamide (C
18), arachidonamide (C
20) and erucamide (C
22). It is even more preferred that the fatty acid amides are monounsaturated fatty
acid amides, preferably containing 18 to 22 carbon atoms such as oleamide and erucamide.
[0021] The amount of the fatty acid amide in the compositions of the invention is typically
from 0.01 wt.% to 2.0 wt.%, preferably from 0.05 wt.% to 1.5 wt.% and more preferably
from 0.1 to 1.0 wt.%, based on the total weight of the lubricating composition.
[0022] According to a preferred embodiment according to the present invention, the lubricating
composition further comprises a polyol ester. There are no particular limitations
regarding the polyol esters as used in lubricating composition according to the present
invention and various conventional polyol esters may be conveniently used.
[0023] Preferably, the polyol ester according to the present invention is a polyol ester
of an aliphatic carboxylic acid having 12 to 24 carbon atoms, more preferably 14 to
20 carbon atoms, most preferably 16 to 18 carbon atoms. The polyol moiety of the polyol
ester may include polyols such as diols, triols and the like such as ethylene glycol,
propylene glycol, glycerol, sorbitol, etc.
[0024] Examples of the carboxylic acid moiety of the polyol ester include octadecanoic acid,
oleic acid, hexadecanoic acid, dodecanoic acid, tetradecanoic acid and iso-forms thereof
(i.e. having branched carbon chains). Preferably the carboxylic acid moiety of the
polyol ester is a fatty acid.
[0025] The polyol esters used in the present invention may be mixtures of mono-, di- and
trimesters, but preferably are predominantly the monoesters.
[0026] It is even more preferred that the polyol ester is a polyol monoester of an iso-fatty
acid (i.e. a branched fatty acid) such as glycerol mono-isostearate, which is commercially
readily available. Other polyol esters such as the oleic acid monoester of glycerol
may be conveniently used as well.
[0027] The amount of the polyol ester in the compositions of the invention is typically
from 0.01 wt.% to 2.0 wt.%, preferably from 0.2 wt.% to 1.2 wt.% and more preferably
from 0.4 to 0.8 wt.%, based on the total weight of the lubricant composition.
[0028] The lubricating composition according to the present invention may further comprise
one or more other additives such as anti-oxidants, anti-wear additives, dispersants,
detergents, overbased detergents, extreme pressure additives, other friction modifiers,
viscosity modifiers, pour point depressants, metal passivators, corrosion inhibitors,
demulsifiers, anti-foam agents, seal compatibility agents and additive diluent base
oils, etc.
[0030] The lubricating compositions of the present invention may be conveniently prepared
by admixing the one or more additives with the base oil(s).
[0031] The above-mentioned additives are typically present in an amount in the range of
from 0.01 to 35.0 wt.%, based on the total weight of the lubricating composition,
preferably in an amount in the range of from 0.05 to 25.0 wt.%, more preferably from
1.0 to 20.0 wt.%, based on the total weight of the lubricating composition.
[0032] According to a preferred embodiment of the present invention, the lubricating composition
has a sulphated ash content (according to ASTM D 874) of at most 1.2 wt.%, preferably
at most 0.90 wt%, more preferably at most 0.50 wt.%.
[0033] Further it is preferred that the composition has a total base number (TBN) value
(according to ASTM D 2896) of between 4.0 and 12.0 mg KOH/g.
[0034] Moreover, the lubricating composition according to the present invention preferably
has a calcium content (according to ASTM D 4951) of at most 0.25 wt.%.
[0035] Typically, the kinematic viscosity 100°C (according to ASTM D 445) of the composition
according to the present invention is between 9.3 and 26.1 cSt, preferably above 9.3
and below 16.3 cSt.
[0036] In another aspect, the present invention provides the use of a lubricating composition
according to the present invention, in particular in a gas engine, in order to improve
the friction reduction properties (in particular according to the SRV test of DIN
51834-1).
[0037] The lubricating compositions according to the present invention are useful for lubricating
apparatus generally, but in particular for use as engine oils for internal combustion
engines. These engine oils include passenger car engines, diesel engines, marine diesel
engines, gas engines, two- and four-cycle engines, etc., and in particular gas engines.
[0038] The present invention is described below with reference to the following Examples,
which are not intended to limit the scope of the present invention in any way.
Examples
Lubricating Oil Compositions
[0039] Various lubricating compositions for use in a gas engine were formulated.
[0040] Table 1 indicates the composition and properties of the fully formulated gas engine
oil formulations that were tested; the amounts of the components are given in wt.%,
based on the total weight of the fully formulated formulations.
[0041] All tested gas engine oil formulations were formulated as SAE 40 formulations meeting
the so-called SAE J300 Specifications (as revised in May 2004; SAE stands for Society
of Automotive Engineers).
[0042] All the tested gas engine oil formulations contained a combination of a base oil,
an additive package and - if present - a total amount of 1.5 wt.% of one or more friction
modifiers, based on the total weight of the composition.
[0043] The additive packages contained a combination of additives including anti-oxidants,
zinc-based anti-wear additives, an ashless dispersant, overbased and ashless detergents,
a pour point depressant, a corrosion inhibitor and a metal passivator.
[0044] "Additive package 1" and "Additive package 2" were so-called Low Ash additive packages,
i.e. resulting in a total Sulfated Ash content of 0.50 wt.%; "Additi-cre package 1"
provided a TBN of about 4.5 mg KOH/g (according to ASTM D 2896), whereas "Additive
package 2" provided a TBN of about 9.0 mg KOH/g.
[0045] "Additive package 3" was a so-called Medium Ash additive package, i.e. resulting
in a total Sulfated Ash content of 0.90 wt.%.
[0046] "Base oil 1" was a commercially available Group II base oil having a kinematic viscosity
at 100°C (ASTM D445) of approx. 12.4 cSt (mm
2s
-1). Base oil 1 is commercially available from e.g. Chevron Products Company (San Ramon,
CA, United States) (under the trade designation "Chevron 600 R").
[0047] "Base oil 2" was a Fischer-Tropsch derived base oil ("GTL 8") having a kinematic
viscosity at 100°C (ASTM D445) of approx. 8 cSt (mm
2s
-1). This GTL base oil may be conveniently manufactured similar to the process as described
in e.g.
WO 02/070631, the teaching of which is hereby incorporated by reference.
[0048] "Base oil 3" was a commercially available Group I base oil having a kinematic viscosity
at 100°C (ASTM D445) of approx. 11.2 cSt (mm
2s
-1). Base oil 3 is commercially available from e.g. Shell Chemicals under the trade
designation "Catenex".
[0049] "Friction modifier 1" (hereafter "FM 1") was a molybdenum-containing dithiocarbamate
compound. FM 1 is commercially available from e.g. Infineum International Ltd (Abingdon,
United Kingdom) under the trade designation "Infineum C9455".
[0050] "Friction modifier 2" (hereafter "FM 2") was a fatty acid amide, more specifically
an oleamide. FM 2 is commercially available from e.g. Croda Oleochemicals (Hull, United
Kingdom) under the trade designation "Crodamide O".
[0051] "Friction modifier 3" (hereafter "FM 3") was a polyol ester, more specifically a
glycerol mono-isostearate (i.e. a glycerol monoester of an iso-fatty acid). FM 3 is
commercially available from e.g. Croda International Plc (Snaith, United Kingdom)
under the trade designation "Prisorine 2040".
[0052] "Friction modifier 4" (hereafter "FM 4") was a polyol ester, more specifically a
glycerol mono-octadecanoate. FM 4 is commercially available from e.g. Croda International
Plc (Snaith, United Kingdom) under the trade designation "Perfad 3336".
[0053] The compositions of Examples 1-5 and Comparative Examples 1-5 were obtained by mixing
the base oils with the additive package and friction modifier(s) using conventional
lubricant blending procedures.
Table 1
| Component [we.%] |
Example 1 |
Example 2 |
Example 3 |
Example 4 |
Example 5 |
Comp. Ex. 1 |
Comp. Ex. 2 |
Comp. Ex. 3 |
Comp. Ex. 4 |
Comp. Ex. 5 |
| Base oil 1 (Group II) |
89.50 |
89.50 |
- |
- |
89.50 |
91.00 |
89.50 |
89.50 |
89.50 |
89.50 |
| Base oil 2 (GTL 8) |
- |
- |
89.50 |
- |
- |
- |
- |
- |
- |
- |
| Base oil 3 (Group I) |
- |
- |
- |
86.70 |
- |
- |
- |
- |
- |
- |
| Additive package 1 |
9.00 |
- |
- |
- |
9.00 |
9.00 |
9.00 |
9.00 |
9.00 |
9.00 |
| Additive package 2 |
- |
9.00 |
9.00 |
- |
- |
- |
- |
- |
- |
- |
| Additive package 3 |
- |
- |
- |
11.80 |
- |
- |
- |
- |
- |
- |
| FM 1 (Mo-compound) |
0.60 |
0.60 |
0.60 |
0.60 |
0.60 |
- |
0.75 |
0.75 |
- |
- |
| FM 2 (Fatty acid amide; i.c. oleamide) |
0.30 |
0.15 |
0.15 |
0.15 |
0.30 |
- |
- |
- |
0.75 |
1.50 |
| FM 3 (polyol ester; i.c. glycerol mono-isostearate) |
0.60 |
0.75 |
0.75 |
0.75 |
- |
- |
0.75 |
- |
0.75 |
- |
| FM 4 (polyol ester; i.c. glycerol mono-octadecanoate) |
- |
- |
- |
- |
0.60 |
- |
- |
0.75 |
- |
- |
| TOTAL |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
100 |
| Properties of the formulated lubricating composition |
| Component [wt.%] |
Example 1 |
Example 2 |
Example 3 |
Example 4 |
Example 5 |
Comp. Ex. 1 |
Comp. Ex. 2 |
Comp. Ex. 3 |
Comp. Ex. 4 |
Comp. Ex. 5 |
| Sulfated ash content1 [wt.%] |
0.50 |
0.48 |
0.48 |
0.90 |
0.50 |
0.49 |
0.50 |
0.50 |
0.50 |
0.50 |
| TBN value2 [mg KOH/g] |
4.56 |
9.00 |
9.00 |
8.76 |
4.54 |
4.56 |
4.56 |
4.56 |
4.53 |
4.44 |
| Kinematic viscosity at 100°C3 [cSt] |
13.55 |
13.52 |
13.70 |
13.75 |
13.42 |
13.71 |
13.46 |
13.48 |
13.57 |
13.45 |
| Kinematic viscosity at 40°C3 [cSt] |
126.7 |
126.6 |
97.0 |
133.5 |
124.8 |
128.0 |
125.2 |
125.7 |
127.0 |
124.9 |
| Ca content4 [wt.%] |
0.14 |
0.13 |
0.13 |
0.25 |
0.14 |
0.14 |
0.14 |
0.14 |
0.14 |
0.14 |
| Zn content4 [wt.%] |
0.03 |
0.03 |
0.03 |
0.03 |
0.03 |
0.03 |
0.03 |
0.03 |
0.03 |
0.03 |
1According to ASTM D 874
2According to ASTM D 2896
3According to ASTM D 445
4Acoording to ASTM D 4951 |
Friction Reduction Properties
[0054] In order to demonstrate the friction reduction properties of the present invention,
measurements were performed according to the SRV-test of DIN 51834-1, whilst following
the ASTM D 6425 prescriptions with respect to test machine and materials. In the test,
the following test conditions were used:
- Load: 50 N
- Temperature: 150°C
- Reciprocating Frequency: 50 Hz
- Stroke length: 1 mm
- Time: 90 minutes.
[0055] The measured friction reduction properties are indicated in Table 2 below. The "normalised
friction coefficient" refers to the relative value when compared to the value of Comparative
Example 1; the lower this normalised friction coefficient is, the more friction reduction
occurs.
Table 2
| |
Example 1 |
Example 2 |
Example 3 |
Example 4 |
Example 5 |
Comp. Ex. 1 |
Comp. Ex. 2 |
Comp. Ex. 3 |
Comp. Ex. 4 |
Comp. Ex. 5 |
| Friction coefficient |
0.051 |
0.066 |
0.06 |
0.047 |
0.075 |
0.157 |
0.087 |
0.11 |
0.129 |
0.111 |
| Normalised friction coefficient |
32.48 |
42.04 |
38.22 |
29.94 |
47.77 |
100 |
55.41 |
70.06 |
82.17 |
70.70 |
| Friction reduction [%] |
67.52 |
57.96 |
61.78 |
70.06 |
52.23 |
0 |
44.59 |
29.94 |
17.83 |
29.30 |
Discussion
[0056] As can be learned from Table 2, the friction reduction values for the compositions
according to the present invention were significantly improved when compared with
Comparative Example 1 (containing no friction modifier) and Comparative Example 2
and 3 (containing the same amount of friction modifier but no fatty acid amide such
as an oleamide). This is a clear indication of desirable friction reduction properties
for the compositions according to the present invention.
[0057] Also, friction reduction values for the Examples according to the present invention
were also significantly improved when compared with Comparative Example 4 (containing
the same fatty acid amide and polyol ester but no molybdenum compound) and Comparative
Example 5 (containing only a fatty acid amide).
[0058] Also, as can be learned from Tables 1 and 2, the present invention surprisingly allows
formulating suitable gas engine oil compositions having a low sulphated ash content
and both low (Examples 1 and 5) or high (Examples 2-4) TBN-values. In this respect
it is noted that usually the performance of a friction modifier combination varies
with the specific formulation used; however, the combination according to the present
invention appears to perform consistently good.
[0059] From the comparison between Example 1 and Example 5 (differing only in the polyol
ester) it can be learned that according to the present invention there is a preference
for a polyol ester of a branched fatty acid (glycerol mono-isostearate) above a polyol
ester of an unbranched fatty acid (glycerol mono-octadecanoate).
1. A lubricating composition comprising:
- a base oil;
- a molybdenum-containing compound; and
- a fatty acid amide.
2. Lubricating composition according to claim 1, wherein the molybdenum-containing compound
is a sulphur-containing molybdenum-containing compound.
3. Lubricating composition according to claim 2, wherein the molybdenum-containing compound
is a dithiocarbamate compound.
4. Lubricating composition according to any of claims 1 to 3 wherein the composition
comprises at least 0.40 wt.%, more preferably at least 0.45 wt.%, even more preferably
at least 0.50 wt.% of the molybdenum-containing compound.
5. Lubricating composition according to any of claims 1 to 4, wherein the fatty acid
amide contains from 12 to 26 carbon atoms, preferably from 16 to 24 carbon atoms,
more preferably from 18 to 22 carbon atoms.
6. Lubricating composition according to any of claims 1 to 5, further comprising a polyol
ester.
7. Lubricating composition according to claim 6, wherein the polyol ester is a polyol
ester of an aliphatic carboxylic acid containing from 12 to 24 carbon atoms.
8. Lubricating composition according to claim 6 or 7, wherein the polyol ester is a polyol
monoester of an iso-fatty acid, preferably containing from 14 to 20 carbon atoms,
more preferably from 16 to 18 carbon atoms.
9. Use of a lubricating composition according to any of claims 1 to 8, in particular
in a gas engine, in order to improve friction reduction properties (in particular
according to the SRV test of DIN 51834-1).