U.S. patent application number 10/966469 was filed with the patent office on 2005-06-23 for lubricating compositions.
This patent application is currently assigned to Infineum USA LP. Invention is credited to Field, Ian Peter, Tamigniau, Etienne Marc.
Application Number | 20050137099 10/966469 |
Document ID | / |
Family ID | 8229534 |
Filed Date | 2005-06-23 |
United States Patent
Application |
20050137099 |
Kind Code |
A1 |
Field, Ian Peter ; et
al. |
June 23, 2005 |
Lubricating compositions
Abstract
A synthetic ester-containing lubricant with good soot-handling
and, with friction modifier, viscosity modifier and antioxidant
present, improved engine performance and cleanliness.
Inventors: |
Field, Ian Peter; (Abingdon,
GB) ; Tamigniau, Etienne Marc; (Tilly, BE) |
Correspondence
Address: |
STOUT, UXA, BUYAN & MULLINS LLP
4 VENTURE, SUITE 300
IRVINE
CA
92618
US
|
Assignee: |
Infineum USA LP
Linden
NJ
Fina Research S.A.
Seneffe
|
Family ID: |
8229534 |
Appl. No.: |
10/966469 |
Filed: |
October 14, 2004 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10966469 |
Oct 14, 2004 |
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10235466 |
Sep 5, 2002 |
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6844301 |
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10235466 |
Sep 5, 2002 |
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09539220 |
Mar 30, 2000 |
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09539220 |
Mar 30, 2000 |
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PCT/GB98/02947 |
Oct 1, 1998 |
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Current U.S.
Class: |
508/495 ;
508/485; 508/562; 508/584; 508/591 |
Current CPC
Class: |
C10N 2030/52 20200501;
C10M 129/10 20130101; C10M 2229/02 20130101; C10M 2203/06 20130101;
C10M 2207/281 20130101; C10N 2040/25 20130101; C10M 2203/1025
20130101; C10M 2205/04 20130101; C10M 2229/05 20130101; C10N
2040/252 20200501; C10M 2203/1006 20130101; C10M 2205/028 20130101;
C10M 2207/023 20130101; C10N 2020/02 20130101; C10N 2040/251
20200501; C10M 2203/1085 20130101; C10M 2207/283 20130101; C10M
143/12 20130101; C10M 2207/34 20130101; C10N 2030/02 20130101; C10M
133/08 20130101; C10M 2205/026 20130101; C10M 2207/282 20130101;
C10M 2207/286 20130101; C10M 2223/04 20130101; C10N 2040/255
20200501; C10N 2040/28 20130101; C10M 105/38 20130101; C10M
2203/1045 20130101; C10M 2215/042 20130101; C10M 2205/06 20130101;
C10M 129/74 20130101; C10M 2203/1065 20130101; C10M 2207/026
20130101; C10N 2040/253 20200501; C10M 101/02 20130101; C10M 169/04
20130101; C10M 159/20 20130101; C10M 2207/2835 20130101; C10M
2207/027 20130101; C10M 2207/26 20130101; C10M 2223/042 20130101;
C10M 2219/106 20130101 |
Class at
Publication: |
508/495 ;
508/485; 508/562; 508/584; 508/591 |
International
Class: |
C10M 129/74 |
Foreign Application Data
Date |
Code |
Application Number |
Oct 3, 1997 |
EP |
EP 97 307 845.4 |
Claims
1-75. (canceled)
76. A method of improving the ability of a lubricant composition to
retain particulate products of fuel combustion in suspension, the
method comprising adding to the lubricant from 5 to 50% by weight,
based on the total weight of the composition, of an ester effective
to improve the ability of the composition to retain said
particulate products in suspension, the ester being an ester of a
carboxylic acid, having at most 30 carbon atoms, and an alcohol,
the ester being substantially free from unreacted alcohol moieties
and having a molecular weight within the range of from 400 to
5000.
77. The method as claimed in claim 76, wherein the composition
contains from 10 to 40% of the ester.
78. The method as claimed in claim 76, wherein the composition
contains from 15 to 30% of the ester.
79. The method as claimed in claim 76, wherein the molecular weight
of the ester is at least 450.
80. The method as claimed in claim 76, wherein the molecular weight
of the ester is within the range of from 500 to 750.
81. The method as claimed in claim 76, wherein the ester is an
ester of a polyhydric alcohol and a monocarboxylic acid.
82. The method as claimed in claim 76, wherein the ester is an
ester of trimethylol propane and a mixture of C8 to C10 alkanoic
acids.
83. The method as claimed in claim 76, wherein the composition is a
crankcase lubricant.
84. The method as claimed in claim 76, wherein the composition is a
compression-ignited engine crankcase lubricant.
85. The method as claimed in claim 76 wherein the composition
comprises an API Group III base stock.
86. The method as claimed in claim 76, wherein the composition
comprises a hydroisomerized base stock.
Description
[0001] This is a continuation of PCT/GB98/02947, filed Oct. 1,
1998, which claims priority to EP 97307845.4, filed Oct. 3, 1997.
The above applications are expressly incorporated herein by
reference in their entirety.
[0002] This invention relates to lubricating compositions, more
especially to compositions suitable for use in piston engine,
especially diesel (compression-ignited) engine, crankcase
lubrication. The invention also relates to the use of certain
components to give improved properties in certain respects.
[0003] There is an increasing demand for improvement in efficiency
and useful life of oil-based lubricants. A factor substantially
shortening the useful life of a lubricating composition is
oxidation. This results in the formation of acids, which tend to
corrode engine parts, and in an unwanted viscosity increase, which
reduces the utility of the composition as a lubricant.
[0004] A primary purpose of a lubricant is to reduce the friction
between moving parts; in a crankcase lubricant friction reduction
results in lower engine wear and improved engine efficiency.
[0005] A further purpose of a crankcase lubricant is to maintain in
suspension any by-products of combustion that find their way into
the crankcase, preventing the formation of sludge and deposits that
would otherwise foul the engine.
[0006] There remains a need for improvement in all these functions
and properties of lubricant compositions.
[0007] The present invention provides the use, to improve the
ability of a lubricant composition to retain particulate combustion
products in suspension, of an ester of a carboxylic acid having at
most 30 carbon atoms and an alcohol, the ester having a molecular
weight within the range of from 400 to 5000. More especially, the
invention provides the use of such an ester to improve the soot
handling characteristics of the composition.
[0008] Mixtures of esters may be used provided their weight average
molecular weight is or their characteristics are within the desired
ranges. In many embodiments this may result from the use as acid
and/or alcohol component of a product derived from a natural
(animal or vegetable) source, or from petroleum base stock, in
which case the component will be a mixture of materials with a
narrow range of molecular weights. In other embodiments, the
mixture may be of materials of widely differing molecular weights
as when, for example, a small proportion of lower or higher ester
is added to adjust the properties, e.g., the viscosity, of the
ester component or of the total lubricant composition.
[0009] Advantageously, the molecular weight of the ester or the
weight average molecular weight of the ester mixture is at most
2000, more advantageously within the range of from 400 to 1000,
preferably from 450 to 1000 and most preferably from 500 to
750.
[0010] The ester is advantageously obtainable by reaction of one or
more carboxylic acids and one or more alcohols, more especially by
reaction of a polycarboxylic acid and a monohydric alcohol or,
preferably, a polyhydric alcohol and a monocarboxylic acid.
Advantageously, the ester is an aliphatic, preferably a saturated
aliphatic, ester.
[0011] The alcohol advantageously contains from 2 to 8, preferably
from 3 to 6, and most preferably 3 or 4, esterifiable hydroxyl
groups, and advantageously contains from 2 to 10, preferably 5 or
6, carbon atoms. The polyol is advantageously trimethylolpropane,
pentaerythritol, neopentyl glycol, or dimethylolpropane. The polyol
may contain one or more, advantageously 1 or 2, ether functions;
examples of such compounds are oligomers of the above-mentioned
polyols, e.g., di- or tri-pentaerythritol. Cycloaliphatic polyols
may be used but aliphatic polyols are presently preferred,
especially trimethylolpropane. The acid advantageously contains at
most 24, more advantageously from 6 to 18, carbon atoms, including
the carboxyl carbon atom, and preferably from 8 to 12, most
preferably from 8 to 10, carbon atoms, and, as indicated above,
advantageously contains a single carboxylic group.
[0012] As acids there are advantageously used aliphatic acids,
preferably saturated aliphatic acids. As examples there may be
mentioned hexanoic, heptanoic, octanoic, nonanoic, decanoic,
dodecanoic, and stearic acids. The acid may be linear or branched;
mixtures of acids may be preferred primarily for reasons of
availability. In embodiments in which a polyol is employed, it may
be esterified with a mixture of mono- and poly-carboxylic acids,
the latter advantageously in a minor proportion, to give a
so-called complex ester. Similarly, a polycarboxylic acid may be
used with a mixture of mono- and poly-ols.
[0013] Advantageously, the ester is substantially free from
unreacted alcohol and acid moieties; advantageously the acid number
of the ester is at most 5, preferably at most 1, mg KOH/g.
[0014] Advantageously, the pour point of the ester, as measured by
ASTM D97, is at most -15.degree. C., preferably at most -21.degree.
C. Its viscosity at 100.degree. C. is advantageously within the
range of from 3 to 12, and preferably within the range of from 4 to
8, mm.sup.2/sec or cSt. Its viscosity index is advantageously at
least 120, preferably from 130 to 160, as measured by ASTM
D2270.
[0015] The invention accordingly also provides the use, to improve
the ability of a lubricant composition to retain particulate
combustion products, especially soot, in suspension, of an ester
having an ASTM D97 pour point of at most -15.degree. C., a
viscosity at 100.degree. C. within the range of from 3 to 12
mm.sup.2/sec, and an ASTM D2270 viscosity index of at least 120.
Advantageously the ester has an acid number of at most 5 mg KOH/g,
and preferably its chemical constitution is as defined and
described above.
[0016] A presently preferred ester is trimethylolpropane esterified
by mixed C.sub.8 to C.sub.10 alkanoic acids, such as the ester
commercially available from FINA Chemicals as Radialube 7368.
Radialube is a trade mark.
[0017] As will be discussed in more detail below, a typical
lubricant composition will contain, in addition to a natural and/or
synthetic base stock, various additives among which may be
mentioned detergents, dispersants, antioxidants, antiwear agents,
corrosion inhibitors, friction modifiers, rust inhibitors, pour
point depressants, viscosity modifiers and antifoams. Two or more
materials in each functional category may be used, and a given
material may be effective in more than one functional category.
[0018] It has been found that the friction-reducing properties of
the lubricant of the present invention may be improved by the
incorporation of an amine-based friction modifier.
[0019] The invention accordingly further provides a lubricant
composition comprising an ester as defined above and an amine-based
friction modifier, the composition containing from 5 to 50% by
weight of the ester, based on the total weight of the
composition.
[0020] The invention also further provides the use, to improve the
friction-reducing properties of a lubricant composition, of an
ester as defined above and an amine-based friction modifier.
[0021] It has also been found that the oxidation stability and
deposit control of the ester-containing lubricant of the present
invention may be improved by the incorporation of a viscosity
modifier, more especially an alkenyl arene/diene copolymer
viscosity modifier, otherwise known as a viscosity index improver,
and an antioxidant, more especially a hindered phenol
antioxidant.
[0022] The invention still further provides a lubricant composition
comprising an ester as defined, an alkylene arene/diene copolymer
viscosity modifier, and a hindered phenol antioxidant, the
composition containing from 5 to 50% by weight of the ester, based
on the total weight of the composition.
[0023] The invention also provides the use, to improve the control
of piston deposits in a diesel (compression-ignited) engine, of a
lubricant composition containing an ester as defined, a viscosity
modifier as defined and a hindered phenol antioxidant.
[0024] It will be appreciated that advantageously the lubricant
composition will contain both the friction-reducing and the deposit
controlling components.
[0025] In all embodiments of the invention, the ester is
advantageously present in a proportion of from 5% to 50%,
preferably from 10% to 40%, and most preferably from 15% to 30%, by
weight of the total composition.
[0026] The base stock may comprise, in addition to the ester
provided according to the invention, other synthetic base stocks,
including esters other than those as defined above;
poly-.alpha.-olefins, polybutenes, alkyl benzenes, alkylated
naphthalenes, esters of phosphoric acids and polysilicone oils, as
well as natural base stocks.
[0027] Natural base stocks, within Group I, II, or III of the API
EOLCS 1509 definition, include mineral lubricating oils which may
vary widely as to their crude source, for example, as to whether
they are paraffinic, naphthenic, mixed, or paraffinic-naphthenic,
as well as to the method used in their production, for example,
their distillation range and whether they are straight run or
cracked, hydrofined, or solvent extracted.
[0028] An API Group III base stock, for example a hydrocracked or
hydroisomerized base stock, is preferred, a hydroisomerized base
stock being especially preferred. The base stock or base stocks,
other than the ester provided by the invention, together with any
of the additives present, make up the balance of the
composition.
[0029] The invention is especially applicable to compositions which
contain, in addition to the ester as defined above, an API Group
III base stock, especially a hydroisomerized base stock, and a
detergent in a proportion that gives an ash content of at least
1.5%, advantageously in the range of from 1.5% to 7%, and and
preferably from 1.5% to 3%, most preferably from 1.8% to 3%, by
weight.
[0030] The lubricating oil base stock mixture conveniently has a
viscosity of 2.5 to 12 cSt, or mm.sup.2/s, and preferably 3.5 to 9
cSt., or mm.sup.2/s, at 100.degree. C., the actual value depending
on the lubricant grade being manufactured.
[0031] As the amine-based friction modifier, there may be mentioned
more especially a tertiary amine. Examples of suitable tertiary
amines are given in International Applications Nos. WO 93/21288 and
WO 97/040050, the disclosures of which are incorporated by
reference herein. Advantageously there is used a compound of the
formula 1
[0032] wherein R.sup.1 represents an alkyl group, R.sup.2
represents hydrogen or an alkyl group, and m, n, and p
independently represent an integer within the range of from 1 to 4.
Advantageously, the alkyl group(s) contain(s) from 12 to 20 carbon
atoms. Advantageously m and p represent 2, n represents 2 or 3, and
R.sup.2 represents hydrogen. Especially preferred friction
modifiers are N-(2-hydroxyethyl)-N-(2-tallo-
woxyethyl)-2-aminoethanol, and
N-(2-hydroxyethyl)-N-(3-tallowoxypropyl)-2-- aminoethanol, wherein
tallow represents a natural product comprising predominantly
C.sub.16 and C.sub.18 alkyl groups.
[0033] The friction modifier is advantageously present in a
proportion of from 0.025% to 1.0%, preferably from 0.05% to 0.25%,
more preferably from 0.075% to 0.15%, by weight of the total
composition.
[0034] Viscosity modifiers impart high and low temperature
operability to a lubricating oil and permit it to remain shear
stable at elevated temperatures and also exhibit acceptable
viscosity or fluidity at low temperatures.
[0035] As the alkenyl arene/diene copolymer viscosity modifier,
there may be mentioned, more especially, hydrogenated copolymers,
in which advantageously at least 80%, preferably from 90 to 98%, of
the residual unsaturation has been removed. As preferred examples
of the copolymers there may be mentioned block copolymers, for
example di- and tri-block copolymers. As examples of such
copolymers there may be mentioned styrene, including
alkyl-substituted styrene, and isoprene copolymers. Other
conjugated dienes, e.g., butadiene, may also or instead be used. A
typical weight average molecular weight range for the polymer is
from 10,000 to 100,000, preferably from 70,000 to 100,000. As
further examples of suitable copolymers, there may be mentioned
star copolymers, which typically have a core of an alkenyl arene
polymer, e.g., of divinyl benzene, and a number of pendant arms,
typically 4 to 25, more especially 12 to 16, arms, provided by, for
example, a diene polymer, e.g., of isoprene, advantageously
hydrogenated, each arm typically having a molecular weight of from
30,000 to 50,000, and the star polymer typically having a molecular
weight of from 500,000 to 620,000. The free ends of the arms may
carry functional groups.
[0036] Advantageously, the copolymer is a hydrogenated
styrene/diene, preferably styrene/isoprene block copolymer.
[0037] The viscosity modifier is advantageously present in a
proportion of from 0.05% to 2%, preferably from 0.1% to 1.5%, more
preferably from 0.75% to 1.25%, by weight, based on the total
composition.
[0038] Antioxidants reduce the tendency of mineral oils to
deteriorate in service, evidence of such deterioration being, for
example, the production of varnish-like deposits on metal surfaces
and of sludge, and viscosity increase.
[0039] As hindered phenol antioxidant, there is advantageously used
one of the formula 2
[0040] wherein R.sup.3 represents a tertiary butyl group, and
R.sup.4 represents alkyl, optionally interrupted by a hetero atom,
preferably sulphur, CH.sub.2-aryl, aryl, or
(CH.sub.2).sub.nCOOR.sup.5, in which n represents 1 to 4 and
R.sup.5 represents an alkyl group. When R.sup.4represents an alkyl
group it advantageously contains from 6 to 20 carbon atoms.
Advantageously n represents 2, and advantageously R.sup.5
represents an alkyl group containing from 6 to 10, preferably 7 to
9, carbon atoms. A preferred antioxidant is Irganox (TM) L135, in
which R.sup.4 represents CH.sub.2CH.sub.2COOR.sup.5, R.sup.5 being
a mixture of C.sub.8 alkyl groups. Other suitable antioxidants
include hindered bis-phenols, many of which are known and commonly
used in the art.
[0041] The proportion of hindered phenolic antioxidant will depend
largely on its potency. In general, however, it is advantageously
present in a proportion of at least 0.25%, more advantageously from
0.5% to 5%, preferably from 1.0% to 4%, and most preferably from
1.5% to 3.5%, by weight based on the total weight of the
composition.
[0042] The lubricant compositions of the invention are especially
suitable for use as compression-ignited (diesel) engine crankcase
lubricants, for example automobile and truck engines, as well as
marine and railroad diesel engines, and the invention also provides
a process for lubricating such an engine which comprises supplying
to the engine a lubricant according to the invention and operating
the engine.
[0043] In addition to the additives provided in accordance with the
invention, the lubricant composition may comprise one or more of
the following components:
[0044] Suitable viscosity modifiers, in addition to one provided in
accordance with the invention, are generally high molecular weight
hydrocarbon polymers or polyesters, and viscosity index improver
dispersants, which function as dispersants as well as viscosity
index improvers. Oil-soluble viscosity modifying polymers generally
have weight average molecular weights of from about 10,000 to
1,000,000, preferably 20,000 to 500,000, as determined by gel
permeation chromatography or light scattering methods.
[0045] Corrosion inhibitors reduce the degradation of metallic
parts contacted by the lubricating oil composition. Thiadiazoles,
for example those disclosed in U.S. Pat. Nos. 2,719,125, 2,719,126
and 3,087,932, are examples of corrosion inhibitors for lubricating
oils. A preferred thiadiazole is bis-2,5-(nonyl
disulphide)-1,3,4-thiadiazole.
[0046] Suitable antioxidants, in addition to one provided in
accordance with the invention, include alkaline earth metal salts
of alkyl-phenolthioesters; diphenylamines; phenyl-naphthylamines;
and phosphosulphurized or sulphurized hydrocarbons.
[0047] Friction modifiers, in addition to one provided in
accordance with the invention, and fuel economy agents which are
compatible with the other ingredients or the final oil may also be
included. Examples of such materials are glyceryl monoesters of
higher fatty acids, dithiocarbamates, especially the molybdenum
salts, and oxazoline compounds.
[0048] Dispersants maintain oil-insoluble substances, resulting
from oxidation during use, in suspension in the fluid, thus
preventing sludge flocculation and precipitation or deposition on
metal parts. So-called ashless dispersants are organic materials
which form substantially no ash on combustion, in contrast to
metal-containing (and thus ash-forming) detergents. Suitable
dispersants include, for example, derivatives of long chain
hydrocarbon-substituted carboxylic acids in which the hydrocarbon
groups contain 50to 400 carbon atoms, examples of such derivatives
being derivatives of high molecular weight hydrocarbyl-substituted
succinic acid. Such hydrocarbon-substituted carboxylic acids may be
reacted with, for example, a nitrogen-containing compound,
advantageously a polyalkylene polyamine, or with an ester.
Particularly preferred dispersants are the reaction products of
polyalkylene amines with alkenyl succinic anhydrides. Examples of
specifications disclosing dispersants of the last-mentioned type
are U.S. Pat. Nos. 3,202,678, 3,154,560, 3,172,892, 3,024,195,
3,024,237, 3,219,666, 3,216,936 and Belgian Specification No.
662875.
[0049] Other suitable dispersants are the macrocyclic dispersants
disclosed, for example, in U.S. Pat. No. 4,637,886, and aminated
and optionally borated functionalized olefin polymers with at least
30% terminal vinylidene unsaturation, disclosed in WO-94/13709.
[0050] As indicated above, a viscosity index improver dispersant
functions both as a viscosity index improver and as a dispersant.
Examples of viscosity index improver dispersants suitable for use
in lubricating compositions include reaction products of amines,
for example polyamines, with a hydrocarbyl-substituted mono- or
dicarboxylic acid in which the hydrocarbyl substituent comprises a
chain of sufficient length to impart viscosity index improving
properties to the compounds.
[0051] Examples of dispersants and viscosity index improver
dispersants may be found in European Patent Specification No. 24146
B.
[0052] Detergents and metal rust inhibitors include the metal
salts, which may be overbased, of sulphonic acids, alkyl phenols,
sulphurized alkyl phenols, alkyl salicylates, naphthenates, and
other oil-soluble mono- and dicarboxylic acids. Overbased metal
sulphonates wherein the metal is selected from alkaline earth
metals and magnesium are particularly suitable for use as
detergents. Representative examples of detergents/rust inhibitors,
and their methods of preparation, are given in European
Specification No. 208 560 A.
[0053] Antiwear agents, as their name implies, reduce wear of metal
parts. Metal, especially zinc, dihydrocarbyl dithiophosphates
(ZDDPS) are very widely used as antiwear agents. Especially
preferred ZDDPs for use in oil-based compositions are those of the
formula Zn[SP(S)(OR.sup.1)(OR.sup- .2].sub.2 wherein R.sup.1 and
R.sup.2 are independently alkyl or aralkyl groups, advantageously
containing from 1 to 18, and preferably 2 to 12, carbon atoms. If a
material free from phosphorus is required, there may be used, for
example a dithiocarbamate, for example, those described in U.S.
Pat. Nos. 4,758,362 and 4,997,969.
[0054] Pour point depressants, otherwise known as lube oil flow
improvers, lower the temperature at which the fluid will flow or
can be poured. Such additives include copolymers of ethylene and an
.alpha.-olefin or unsaturated ester, polymethacrylates, and
succinic acid-olefin copolymers.
[0055] Foam control may be provided by an antifoam of the
polysiloxane type, for example, silicone oil or polydimethyl
siloxane.
[0056] Some of the above-mentioned additives provide a multiplicity
of effects; thus for example, a single additive may act as a
dispersant-oxidation inhibitor.
[0057] When lubricating compositions contain one or more of the
above-mentioned additives, each additive is typically blended into
the base oil in an amount which enables the additive to provide its
desired function.
[0058] Representative effective amounts of such additives, when
used in crankcase lubricants, are as follows:
1 Mass % a.i.* Mass % a.i.* Additive (Broad) (Preferred) Viscosity
Modifier 0.01-6 0.01-4 Corrosion Inhibitor 0.01-5 0.01-1.5
Oxidation Inhibitor 0.01-6 0.01-4 Friction Modifier 0.01-5 0.01-1.5
Dispersant 0.1-20 0.1-8 Detergents/rust inhibitors.sup.+ 0.01-6
0.01-5 Anti-wear Agent 0.01-6 0.01-4 Pour Point Depressant 0.01-5
0.01-1.5 Anti-Foaming Agent 0.001-3 0.001-0.15 Mineral or Synthetic
Oil Base Balance Balance *Mass % active ingredient based on the
final oil, excluding the additives provided according to the
invention, but may be reduced from the values given if the
invention provides an additive having the same function.
.sup.+Relatively larger proportions, for example at least 10 mass
%, are normally used for marine applications.
[0059] When a plurality of additives is employed it may be
desirable, although not essential, to prepare one or more additive
concentrates comprising the additives (a concentrate sometimes
being referred to as an additive package) whereby several additives
can be added simultaneously to the base oil to form the lubricating
oil composition. Dissolution of the additive concentrate(s) into
the lubricating oil may be facilitated by solvents and by mixing
accompanied with mild heating, but this is not essential.
[0060] It will be understood that the various components or the
composition, the essential components as well as the optional and
customary components, may react under the conditions of
formulation, storage, or use, and that the invention also provides
the product obtainable or obtained as a result of any such
reaction.
[0061] In the following examples, in which all percentages are by
weight, certain tests are referred to. They are carried out as
follows:
[0062] Mack T-8
[0063] This test is carried out in an E7-350 six cylinder Mack
diesel engine with mechanical fuel injection, the timing being
adjusted to give a target level of soot build-up in the lubricant
under test. The engine is run at 1800 rpm, at a fuel flow rate of
63.3 kg/hr, for 250 hours. The test evaluates the ability of an oil
to retain combustion products, typically soot, in suspension, as
demonstrated by reduced viscosity increase and filter plugging when
contaminated with a high level of soot. The maximum viscosity
increase allowed by the API CG-4 and ACEA E3-96 specifications for
one, or the first, test is 11.5 mm.sup.2/sec, or cSt, at a soot
loading of 3.8%. The maximum allowed increase in pressure
differential at that loading is 138 kPa.
[0064] Mercedes Benz OM441LA
[0065] This test is carried out on a six cylinder diesel engine
with rated performance of 250 kW at 1900 rpm, for 400 hours with 50
hours of full load alternating with 50 hours of cyclic conditions,
at an oil sump temperature of 125.degree. C. The engine is
subsequently inspected for engine sludge, piston cleanliness,
engine and turbo housing deposits, visible engine wear, bore
polish, cylinder wear and ring sticking, and the oil consumption is
measured. Sludge, cleanliness, deposits and engine wear are
evaluated on a merit ratings system, and cylinder wear is
measured.
[0066] In Example 1, a composition according to the invention was
compared with a modern European high power diesel lubricating oil,
a 15W40 product meeting the ACEA E3-96 requirement. The oil
contained, by weight, 14.8% Paranox 2281 and 8% Paratone 8002
(Trade Marks) providing an antioxidant and an olefin copolymer
viscosity modifier) in an Esso base stock.
[0067] The composition according to the invention was as
follows:
2 Component Function % Hydroisomerized 44.6 Base Stock (1) Ester
(2) 20.0 Hydrogenated Viscosity Modifier 0.9 Styrene/isoprene
Copolymer (3) Irganox L135 Hindered Phenolic 2.0 Antioxidant Amine
(4) Friction Modifier 0.1 Balance (5) 32.4 (1) Shell XHVI (2)
Trimethylolpropane ester of mixed C.sub.8 to C.sub.10 alkanoic
acids, viscosity at 100.degree. C. 4.5 mm.sup.2/s, VI 140, pour
point <-42.degree. C., acid value 0.1 mg KOH/g. (Radialube (TM)
7368) (3) ASTM D445 viscosity of a 6% solution in mineral oil: 1400
mm.sup.2/s at 100.degree. C. (4)
N-(2-hydroxyethyl)-N-(3-tallowoxypropyl)-2-aminoethanol (5)
Dispersant, ashless and metal detergent, antiwear agent, flow
improver, corrosion inhibitor, other antioxidant, antifoam and
diluents.
[0068] The composition had a viscosity at 100.degree. C. of 12
mm.sup.2 /sec, VI of 175, TBN of 15.3 and an ash content of 1.9% by
weight.
EXAMPLE 1
[0069] The composition according to the invention and the
comparison oil were subjected to the Mack T-8 test to establish
their soot handling abilities; a low viscosity increase and low
change in filter pressure indicate good handling properties. The
table shows the results.
3 Composition Comparison Pass* of Invention Oil Value Viscosity
Increase 3.2 9.3 11.5 at 3.8% soot, mm.sup.2/s Increase in 17 40
138.0 Differential Filter Pressure kPa *ACEA E3-96 pass values
(maximum).
EXAMPLE 2
[0070] The composition of the invention, as set out above, was
subjected to the OM441LA test, and its performance measured against
the Mercedes Benz Page 228.5 specification requirements. The
results shown in the table establish that all criteria are met.
4 Item Rated Target Item Result Cleanliness, Engine 9.0 min 9.4
Cleanliness, Piston 40 min 40 Deposits, % 2.0 max 1.5 Wear, Visual
2.5 max 2.1 Bore Polish 2.0% max 0.3% Cylinder Wear, mm 0.008 max
0.002 Ring Sticking (2nd ring) 1 max 0 Oil Consumption, g/h 100 max
67.7
* * * * *