[0001] This invention relates to lubricating oil compositions including a class of aniline
compounds. The aniline compounds are useful as ashless TBN (Total Base Number) boosters
for lubricating oil compositions, particularly crankcase lubricating oil compositions
having reduced levels of sulfated ash (SASH).
[0002] Environmental concerns have led to continued efforts to reduce the CO, hydrocarbon
and nitrogen oxide (NO
x) emissions from compression ignited (dieselfueled) and spark ignited (gasoline-fueled)
light duty internal combustion engines. Further, there have been continued efforts
to reduce the particulate emissions from compression ignited internal combustion engines.
To meet the upcoming emission standards for heavy duty diesel vehicles, original equipment
manufacturers (OEMs) will rely on the use of additional exhaust gas after-treatment
devices. Such exhaust gas after-treatment devices may include catalytic converters,
which may contain one or more oxidation catalysts, NO
x storage catalysts, and/or NH
3 reduction catalysts; and/or a particulate trap.
[0003] Oxidation catalysts can become poisoned and rendered less effective by exposure to
certain elements/compounds present in engine exhaust gases, particularly by exposure
to phosphorus and phosphorus compounds introduced into the exhaust gas by the degradation
of phosphorus-containing lubricating oil additives. Reduction catalysts are sensitive
to sulfur and sulfur compounds in the engine exhaust gas introduced by the degradation
of both the base oil used to blend the lubricant, and sulfur-containing lubricating
oil additives. Particulate traps can become blocked by metallic ash, which is a product
of degraded metal-containing lubricating oil additives.
[0004] To ensure a long service life, lubricating oil additives that exert a minimum negative
impact on such after-treatment devices must be identified, and OEM specifications
for "new service fill" and "first fill" heavy duty diesel (HDD) lubricants require
maximum sulfur levels of 0.4 mass %; maximum phosphorus levels of 0.12 mass %, and
sulfated ash contents below 1.1 mass %, which lubricants are referred to as "mid-SAPS"
lubricants (where "SAPS" is an acronym for "Sulfated Ash, Phosphorus, Sulfur"). In
the future, OEMs may further restrict these levels maximum levels to 0.08 mass % phosphorus,
0.2 mass % sulfur and 0.8 mass % sulfated ash, with such lubricants being referred
to as "low-SAPS" lubricating oil compositions.
[0005] As the amounts of phosphorus, sulfur and ash-containing lubricant additives are being
reduced to provide mid- and low-SAPS lubricants that are compatible with exhaust gas
after-treatment devices, the lubricating oil composition must continue to provide
the high levels of lubricant performance, including adequate detergency, dictated
by the "new service", and "first fill" specifications of the OEMs, such as the ACEA
E6 and MB p228.51 (European) and API CI-4+ and API CJ-4 (U.S.) specifications for
heavy duty engine lubricants. Criteria for being classified as a lubricating oil composition
meeting the above listed industry standards are known to those skilled in the art.
[0006] The ability of a lubricant to neutralized acidic byproducts of combustion, which
increases in engines provided with exhaust gas recirculation (EGR) systems, particularly
condensed EGR systems in which exhaust gasses are cooled prior to recirculation, can
be improved, and the drain interval of the lubricant can be extended, by increasing
the total base number (TBN) of the composition. Historically, TBN has been provided
by overbased detergents that introduce sulfated ash into the composition. It would
be advantageous to provide a lubricating oil composition with a high level of TBN
using a TBN boosting component that does not contribute sulfated ash. As highly basic
components are known to induce corrosion and, in some cases reduce the compatibility
between lubricating oil compositions and the fluoroelastomeric seal materials used
in engines, it would be preferable to provide such a component that does not induce
corrosion and, preferably, does not adversely affect seals compatibility. Due to demands
for improved fuel economy, less viscous lubricants, such as 0W and 5W 20 and 30 grade
lubricants have become more prevalent. To allow for easier formulation of such lubricants,
the amount of polymer introduced by additives is preferably minimized. Therefore,
it would be further preferable to provide a non-polymeric ashless TBN source.
[0007] US Patent Nos. 5,525,247;
5,672,570; and
6,569,818 are directed to "low ash" lubricating oil compositions in which sulfated ash content
is reduced by replacing overbased detergents with neutral detergents. These patents
describe such lubricants as providing sufficient detergency, but make no claim that
such lubricants will provide sufficient TBN for use, for example, in HDD engines.
US Patent Application 2007/0203031 describes the use of a high TBN nitrogen-containing dispersants as ashless TBN sources.
[0008] US Patent Nos. 4,100,082;
4,200,545;
4,320,021,
4,663,063;
4,708.809; and Russian Patent Application
SU1825780 describe amino-phenol compounds as lubricating oil additives (e.g., dispersant/detergents).
US Patent Nos. 2,511,750;
3,634,248;
4,269,720;
4,335,006;
4,411,805; and
6,242,394 describe certain aniline compounds as stabilizers (antioxidants) for lubricating
oil compositions.
US Patent No. 4,778,654 describes alkylaniline/formaldehyde co-oligomers useful as corrosion inhibitors.
[0009] The present Applicant's co-pending
EP 2 206 764 A1 describes aniline compounds as ashless TBN sources for lubricating oils. A preference
is expressed for di-alkyl substituted aniline compounds where both of the alkyl groups
attached to the nitrogen atom are linear. An example of a di-branched (di-2-ethylhexyl)
compound is provided but there are no data given for its TBN performance in a lubricating
oil.
[0010] It has now been found that certain alkoxy-substituted di-alkyl aniline species are
able to provide improved TBN performance when used as additives for lubricating oils.
Such oil also have enhanched fluoroelastomer seal compatibility, as measured for example
by the VW-6/AK6 test.
[0011] Accordingly in a first aspect, the present invention provides a lubricating oil composition
comprising a major amount of oil of lubricating viscosity and a minor amount of one
or more compounds of formula (I):
wherein R
1, R
2, R
3, R
4 and R
5 independently represent alkyl or substituted alkyl having no aryl substituent.
[0012] The compounds of formula (I) are characterised in that they have two different branched
alkyl groups attached to the nitrogen atom. One of the branched alkyl groups has a
branch at a carbon atom in an α-position to the nitrogen atom and the other has a
branch at a carbon atom in a β-position to the nitrogen atom. It has been found that
this specific configuration provides enhanced TBN performance.
[0013] Preferably, the lubricating oils meet the performance criteria of one or more of
the ACEA E6, MB p228.51, API CI-4+ and API CJ-4 specifications for heavy duty engine
lubricants.
[0014] In accordance with a second aspect, the present invention provides a concentrate
for the preparation of a lubricating oil composition according to any preceding claim,
the concentrate comprising from about 2.5 to about 30 mass % of one or more compounds
of formula (I); about 10 to about 40 mass % of a nitrogen-containing dispersant; about
2 to about 20 mass % of an aminic antioxidant, a phenolic antioxidant, a molybdenum
compound, or a mixture thereof; about 5 to 40 mass % of a detergent; and from about
2 to about 20 mass % of a metal dihydrocarbyl dithiophosphate.
[0015] In accordance with a third aspect of the present invention, there is provided a compound
of formula (I):
wherein R
1, R
2, R
3, R
4 and R
5 independently represent alkyl or substituted alkyl having no aryl substituent.
[0016] In accordance with a fourth aspect of the present invention, there is provided a
method of increasing the TBN of a lubricating oil composition without concurrently
increasing the SASH content, the method comprising adding to the lubricating oil composition
one or more compounds according to the third aspect.
[0017] In accordance with a fifth aspect, the present invention provides the use of a compound
according to the third aspect as an ashless lubricating oil composition TBN source.
[0018] The compounds useful as ashless TBN sources for lubricating oil compositions have
the formula (I):
[0019] Preferably, R
1, R
2, R
3, R
4 and R
5 independently represent alkyl groups.
[0020] Preferably, R
1 represents methyl or ethyl, with methyl being more preferred.
[0021] Preferably, R
3 represents methyl or ethyl, with ethyl being more preferred.
[0022] Embodiments where R
1 and/or R
3 represent longer alkyl groups, for example alkyl groups having 3 to 12 carbon atoms
are also within the scope of the present invention.
[0023] Preferably, R
2 represents an alkyl group having 3 to 12 carbon atoms, which group may be linear
or branched.
[0024] Preferably, R
4 represents an alkyl group having 3 to 12 carbon atoms, which group may be linear
or branched.
[0025] Preferably, R
5 represents methyl or ethyl such that the benzene ring is methoxy or ethoxy substituted.
More preferably, R
5 represents ethyl. Embodiments where R
5 represents a longer alkyl group, for example an alkyl group having 3 to 12 carbon
atoms are also within the scope of the present invention.
[0026] In a preferred embodiment, the compound of formula (I) has the following structure:
[0027] In another preferred embodiment, the compound of formula (I) has the following structure:
[0028] Preferably, the compounds of the present invention have a TBN (as measured in accordance
with ASTM D-2896 and/or ASTM D-4793) of at least about 50, preferably at least about
100, more preferably at least about 140, and most preferably at least about 180 mg
KOH/g.
[0029] Preferably, compounds of the present invention have a >99% weight loss, as determined
by thermal gravity analysis (at 10 °C/min temperature ramp rate in air) at a temperature
of at least about 200, preferably at least about 250, more preferably at least about
300 °C.
[0030] Methods for forming compounds of formula (I) should be apparent to those skilled
in the art. Some suitable methods are described below.
[0031] Aniline and substituted anilines such as ethoxyaniline are commercially available.
N, N-dialkylaniline and substituted derivatives such as N,N-dialkylethoxyaniline can
be prepared by reacting the appropriate aniline or substituted derivatives such as
ethoxyaniline with aldehydes/ketones in a 1:2 or excess molar ratio in the presence
of a reducing agent such as sodium triacetoxyborohydride in dichloromethane solvent.
Such methods are well known and described in the literature, see for example
Jn. Org. Chem (1996), 61, pp. 3489-3862.
[0032] Another method involves reacting the appropriate aniline or substituted aniline with
halogenated alkyl (e.g., brominated alkyl) in a 2:1 molar ratio, in the presence triethylamine,
in an acetonitrile solvent.
[0033] Yet another method reacts aniline or substituted derivatives such as ethoxyaniline
with aldehydes/ketones in a 1:2 or excess molar ratio in the presence of hydrogen
and 10% Pd/C catalyst in methanol solvent. Such methods are well known and a number
of such methods are described, for example, in
US Patent No. 2,045,574.)
[0034] The unsymmetrical compounds of the present invention can be made in analogous manners
using the methods described above and others by employing a step-wise approach whereby
one alkyl group is appended to the nitrogen atom before a second different alkyl group
is attached.
[0035] Oils of lubricating viscosity useful in the context of the present invention may
be selected from natural lubricating oils, synthetic lubricating oils and mixtures
thereof. The lubricating oil may range in viscosity from light distillate mineral
oils to heavy lubricating oils such as gasoline engine oils, mineral lubricating oils
and heavy duty diesel oils. Generally, the viscosity of the oil ranges from about
2 centistokes to about 40 centistokes, especially from about 4 centistokes to about
20 centistokes, as measured at 100°C.
[0036] Natural oils include animal oils and vegetable oils (e.g., castor oil, lard oil);
liquid petroleum oils and hydrorefined, solvent-treated or acid-treated mineral oils
of the paraffinic, naphthenic and mixed paraffinic-naphthenic types. Oils of lubricating
viscosity derived from coal or shale also serve as useful base oils.
[0037] Synthetic lubricating oils include hydrocarbon oils and halo-substituted hydrocarbon
oils such as polymerized and interpolymerized olefins (e.g., polybutylenes, polypropylenes,
propylene-isobutylene copolymers, chlorinated polybutylenes, poly(1-hexenes), poly(1-octenes),
poly(1-decenes)); alkylbenzenes (e.g., dodecylbenzenes, tetradecylbenzenes, dinonylbenzenes,
di(2-ethylhexyl)benzenes); polyphenyls (e.g., biphenyls, terphenyls, alkylated polyphenols);
and alkylated diphenyl ethers and alkylated diphenyl sulfides and derivative, analogs
and homologs thereof. Also useful are synthetic oils derived from a gas to liquid
process from Fischer-Tropsch synthesized hydrocarbons, which are commonly referred
to as gas to liquid, or "GTL" base oils.
[0038] Alkylene oxide polymers and interpolymers and derivatives thereof where the terminal
hydroxyl groups have been modified by esterification, etherification, etc., constitute
another class of known synthetic lubricating oils. These are exemplified by polyoxyalkylene
polymers prepared by polymerization of ethylene oxide or propylene oxide, and the
alkyl and aryl ethers of polyoxyalkylene polymers (e.g., methylpolyiso-propylene glycol
ether having a molecular weight of 1000 or diphenyl ether of poly-ethylene glycol
having a molecular weight of 1000 to 1500); and mono- and polycarboxylic esters thereof,
for example, the acetic acid esters, mixed C
3-C
8 fatty acid esters and C
13 oxo acid diester of tetraethylene glycol.
[0039] Another suitable class of synthetic lubricating oils comprises the esters of dicarboxylic
acids (e.g., phthalic acid, succinic acid, alkyl succinic acids and alkenyl succinic
acids, maleic acid, azelaic acid, suberic acid, sebasic acid, fumaric acid, adipic
acid, linoleic acid dimer, malonic acid, alkylmalonic acids, alkenyl malonic acids)
with a variety of alcohols (e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl
alcohol, ethylene glycol, diethylene glycol monoether, propylene glycol). Specific
examples of such esters includes dibutyl adipate, di(2-ethylhexyl) sebacate, di-n-hexyl
fumarate, dioctyl sebacate, diisooctyl azelate, diisodecyl azelate, dioctyl phthalate,
didecyl phthalate, dieicosyl sebacate, the 2-ethylhexyl diester of linoleic acid dimer,
and the complex ester formed by reacting one mole of sebacic acid with two moles of
tetraethylene glycol and two moles of 2-ethylhexanoic acid.
[0040] Esters useful as synthetic oils also include those made from C
5 to C
12 monocarboxylic acids and polyols and polyol esters such as neopentyl glycol, trimethylolpropane,
pentaerythritol, dipentaerythritol and tripentaerythritol.
[0041] Silicon-based oils such as the polyalkyl-, polyaryl-, polyalkoxy- or polyaryloxysilicone
oils and silicate oils comprise another useful class of synthetic lubricants; such
oils include tetraethyl silicate, tetraisopropyl silicate, tetra-(2-ethylhexyl)silicate,
tetra-(4-methyl-2-ethylhexyl)silicate, tetra-(p-tert-butyl-phenyl) silicate, hexa-(4-methyl-2-ethylhexyl)disiloxane,
poly(methyl)siloxanes and poly(methylphenyl)siloxanes. Other synthetic lubricating
oils include liquid esters of phosphorous-containing acids (e.g., tricresyl phosphate,
trioctyl phosphate, diethyl ester of decylphosphonic acid) and polymeric tetrahydrofurans.
[0042] The oil of lubricating viscosity may comprise a Group I, Group II or Group III, base
stock or base oil blends of the aforementioned base stocks. Preferably, the oil of
lubricating viscosity is a Group II or Group III base stock, or a mixture thereof,
or a mixture of a Group I base stock and one or more a Group II and Group III. Preferably,
a major amount of the oil of lubricating viscosity is a Group II, Group III, Group
IV or Group V base stock, or a mixture thereof. The base stock, or base stock blend
preferably has a saturate content of at least 65%, more preferably at least 75%, such
as at least 85%. Most preferably, the base stock, or base stock blend, has a saturate
content of greater than 90%. Preferably, the oil or oil blend will have a sulfur content
of less than 1%, preferably less than 0.6%, most preferably less than 0.4%, by weight.
[0043] Preferably the volatility of the oil or oil blend, as measured by the Noack volatility
test (ASTM D5880), is less than or equal to 30%, preferably less than or equal to
25%, more preferably less than or equal to 20%, most preferably less than or equal
16%. Preferably, the viscosity index (VI) of the oil or oil blend is at least 85,
preferably at least 100, most preferably from about 105 to 140.
[0044] Definitions for the base stocks and base oils in this invention are the same as those
found in the
American Petroleum Institute (API) publication "Engine Oil Licensing and Certification
System", Industry Services Department, Fourteenth Edition, December 1996, Addendum
1, December 1998. Said publication categorizes base stocks as follows:
- a) Group I base stocks contain less than 90 percent saturates and/or greater than
0.03 percent sulfur and have a viscosity index greater than or equal to 80 and less
than 120 using the test methods specified in Table 1.
- b) Group II base stocks contain greater than or equal to 90 percent saturates and
less than or equal to 0.03 percent sulfur and have a viscosity index greater than
or equal to 80 and less than 120 using the test methods specified in Table 1.
- c) Group III base stocks contain greater than or equal to 90 percent saturates and
less than or equal to 0.03 percent sulfur and have a viscosity index greater than
or equal to 120 using the test methods specified in Table 1.
- d) Group IV base stocks are polyalphaolefins (PAO).
- e) Group V base stocks include all other base stocks not included in Group I, II,
III, or IV.
Table I - Analytical Methods for Base Stock
Property |
Test Method |
Saturates |
ASTM D 2007 |
Viscosity Index |
ASTM D 2270 |
Sulfur |
ASTM D 2622 |
|
ASTM D 4294 |
|
ASTM D 4927 |
|
ASTM D 3120 |
[0045] Lubricating oil compositions of the present invention may further contain one or
more metal-containing or ash-forming detergents. Metal-containing or ash-forming detergents
function both as detergents to reduce or remove deposits and as acid neutralizers
or rust inhibitors, thereby reducing wear and corrosion and extending engine life.
Detergents generally comprise a polar head with a long hydrophobic tail, with the
polar head comprising a metal salt of an acidic organic compound. The salts may contain
a substantially stoichiometric amount of the metal in which case they are usually
described as normal or neutral salts, and would typically have a total base number
or TBN (as can be measured by ASTM D-2896 and/or ASTM D-4793) of from 0 to 80. A large
amount of a metal base may be incorporated by reacting excess metal compound (e.g.,
an oxide or hydroxide) with an acidic gas (e.g., carbon dioxide). The resulting overbased
detergent comprises neutralized detergent as the outer layer of a metal base (e.g.
carbonate) micelle. Such overbased detergents may have a TBN of 150 or greater, and
typically will have a TBN of from 250 to 450 or more. In the presence of the compounds
of formula (I), the amount of overbased detergent can be reduced, or detergents having
reduced levels of overbasing (e.g., detergents having a TBN of 100 to 200), or neutral
detergents can be employed, resulting in a corresponding reduction in the SASH content
of the lubricating oil composition without a reduction in the performance thereof.
[0046] Detergents that may be used include oil-soluble neutral and overbased sulfonates,
phenates, sulfurized phenates, thiophosphonates, salicylates, and naphthenates and
other oil-soluble carboxylates of a metal, particularly the alkali or alkaline earth
metals, e.g., sodium, potassium, lithium, calcium, and magnesium. The most commonly
used metals are calcium and magnesium, which may both be present in detergents used
in a lubricant, and mixtures of calcium and/or magnesium with sodium. Particularly
convenient metal detergents are neutral and overbased calcium sulfonates having TBN
of from 20 to 450 TBN, and neutral and overbased calcium phenates and sulfurized phenates
having TBN of from 50 to 450. Combinations of detergents, whether overbased or neutral
or both, may be used.
[0047] Sulfonates may be prepared from sulfonic acids which are typically obtained by the
sulfonation of alkyl substituted aromatic hydrocarbons such as those obtained from
the fractionation of petroleum or by the alkylation of aromatic hydrocarbons. Examples
included those obtained by alkylating benzene, toluene, xylene, naphthalene, diphenyl
or their halogen derivatives such as chlorobenzene, chlorotoluene and chloronaphthalene.
The alkylation may be carried out in the presence of a catalyst with alkylating agents
having from about 3 to more than 70 carbon atoms. The alkaryl sulfonates usually contain
from about 9 to about 80 or more carbon atoms, preferably from about 16 to about 60
carbon atoms per alkyl substituted aromatic moiety.
[0048] The oil soluble sulfonates or alkaryl sulfonic acids may be neutralized with oxides,
hydroxides, alkoxides, carbonates, carboxylate, sulfides, hydrosulfides, nitrates,
borates and ethers of the metal. The amount of metal compound is chosen having regard
to the desired TBN of the final product but typically ranges from about 100 to 220
mass % (preferably at least 125 mass %) of that stoichiometrically required.
[0049] Metal salts of phenols and sulfurized phenols are prepared by reaction with an appropriate
metal compound such as an oxide or hydroxide and neutral or overbased products may
be obtained by methods well known in the art. Sulfurized phenols may be prepared by
reacting a phenol with sulfur or a sulfur containing compound such as hydrogen sulfide,
sulfur monohalide or sulfur dihalide, to form products which are generally mixtures
of compounds in which 2 or more phenols are bridged by sulfur containing bridges.
[0050] Lubricating oil compositions of the present invention may further contain one or
more ashless dispersants, which effectively reduce formation of deposits upon use
in gasoline and diesel engines, when added to lubricating oils. Ashless dispersants
useful in the compositions of the present invention comprises an oil soluble polymeric
long chain backbone having functional groups capable of associating with particles
to be dispersed. Typically, such dispersants comprise amine, alcohol, amide or ester
polar moieties attached to the polymer backbone, often via a bridging group. The ashless
dispersant may be, for example, selected from oil soluble salts, esters, aminoesters,
amides, imides and oxazolines of long chain hydrocarbon-substituted mono-and polycarboxylic
acids or anhydrides thereof; thiocarboxylate derivatives of long chain hydrocarbons;
long chain aliphatic hydrocarbons having polyamine moieties attached directly thereto;
and Mannich condensation products formed by condensing a long chain substituted phenol
with formaldehyde and polyalkylene polyamine. The most common dispersant in use is
the well known succinimide dispersant, which is a condensation product of a hydrocarbyl-substituted
succinic anhydride and a poly(alkyleneamine). Both mono-succinimide and bis-succinimide
dispersants (and mixtures thereof) are well known.
[0051] Preferably, the ashless dispersant is a "high molecular weight" dispersant having
a number average molecular weight (M
n) greater than or equal to 4,000, such as between 4,000 and 20,000. The precise molecular
weight ranges will depend on the type of polymer used to form the dispersant, the
number of functional groups present, and the type of polar functional group employed.
For example, for a polyisobutylene derivatized dispersant, a high molecular weight
dispersant is one formed with a polymer backbone having a number average molecular
weight of from about 1680 to about 5600. Typical commercially available polyisobutylene-based
dispersants contain polyisobutylene polymers having a number average molecular weight
ranging from about 900 to about 2300, functionalized by maleic anhydride (MW = 98),
and derivatized with polyamines having a molecular weight of from about 100 to about
350. Polymers of lower molecular weight may also be used to form high molecular weight
dispersants by incorporating multiple polymer chains into the dispersant, which can
be accomplished using methods that are know in the art.
[0052] Preferred groups of dispersant include polyamine-derivatized poly α-olefin, dispersants,
particularly ethylene/butene alpha-olefin and polyisobutylene-based dispersants. Particularly
preferred are ashless dispersants derived from polyisobutylene substituted with succinic
anhydride groups and reacted with polyethylene amines, e.g. polyethylene diamine,
tetraethylene pentamine; or a polyoxyalkylene polyamine, e.g. polyoxypropylene diamine,
trimethylolaminomethane; a hydroxy compound, e.g. pentaerythritol; and combinations
thereof. One particularly preferred dispersant combination is a combination of (A)
polyisobutylene substituted with succinic anhydride groups and reacted with (B) a
hydroxy compound, e.g. pentaerythritol; (C) a polyoxyalkylene polyamine, e.g. polyoxypropylene
diamine, or (D) a polyalkylene diamine, e.g. polyethylene diamine and tetraethylene
pentamine using about 0.3 to about 2 moles of (B), (C) and/or (D) per mole of (A).
Another preferred dispersant combination comprises a combination of (A) polyisobutenyl
succinic anhydride with (B) a polyalkylene polyamine, e.g. tetraethylene pentamine,
and (C) a polyhydric alcohol or polyhydroxy-substituted aliphatic primary amine, e.g.
pentaerythritol or trismethylolaminomethane, as described in
U.S. Patent No. 3,632,511.
[0053] Another class of ashless dispersants comprises Mannich base condensation products.
Generally, these products are prepared by condensing about one mole of an alkyl-substituted
mono- or polyhydroxy benzene with about 1 to 2.5 moles of carbonyl compound(s) (e.g.,
formaldehyde and paraformaldehyde) and about 0.5 to 2 moles of polyalkylene polyamine,
as disclosed, for example, in
U.S. Patent No. 3,442,808. Such Mannich base condensation products may include a polymer product of a metallocene
catalyzed polymerization as a substituent on the benzene group, or may be reacted
with a compound containing such a polymer substituted on a succinic anhydride in a
manner similar to that described in
U.S. Patent No. 3,442,808. Examples of functionalized and/or derivatized olefin polymers synthesized using
metallocene catalyst systems are described in the publications identified
supra.
[0054] The dispersant can be further post treated by a variety of conventional post treatments
such as boration, as generally taught in
U.S. Patent Nos. 3,087,936 and
3,254,025. Boration of the dispersant is readily accomplished by treating an acyl nitrogen-containing
dispersant with a boron compound such as boron oxide, boron halide boron acids, and
esters of boron acids, in an amount sufficient to provide from about 0.1 to about
20 atomic proportions of boron for each mole of acylated nitrogen composition. Useful
dispersants contain from about 0.05 to about 2.0 mass %, e.g., from about 0.05 to
about 0.7 mass % boron. The boron, which appears in the product as dehydrated boric
acid polymers (primarily (HBO
2)
3), is believed to attach to the dispersant imides and diimides as amine salts, e.g.,
the metaborate salt of the diimide. Boration can be carried out by adding from about
0.5 to 4 mass %, e.g., from about 1 to about 3 mass % (based on the mass of acyl nitrogen
compound) of a boron compound, preferably boric acid, usually as a slurry, to the
acyl nitrogen compound and heating with stirring at from about 135°C to about 190°C,
e.g., 140°C to 170°C, for from about 1 to about 5 hours, followed by nitrogen stripping.
Alternatively, the boron treatment can be conducted by adding boric acid to a hot
reaction mixture of the dicarboxylic acid material and amine, while removing water.
Other post reaction processes commonly known in the art can also be applied.
[0055] The dispersant may also be further post treated by reaction with a so-called "capping
agent". Conventionally, nitrogen-containing dispersants have been "capped" to reduce
the adverse effect such dispersants have on the fluoroelastomer engine seals. Numerous
capping agents and methods are known. Of the known "capping agents", those that convert
basic dispersant amino groups to non-basic moieties (e.g., amido or imido groups)
are most suitable. The reaction of a nitrogen-containing dispersant and alkyl acetoacetate
(e.g., ethyl acetoacetate (EAA)) is described, for example, in
U.S. Patent Nos. 4,839,071;
4,839,072 and
4,579,675. The reaction of a nitrogen-containing dispersant and formic acid is described, for
example, in
U.S. Patent No. 3,185,704. The reaction product of a nitrogen-containing dispersant and other suitable capping
agents are described in
U.S. Patent Nos. 4,663,064 (glycolic acid);
4,612,132;
5,334,321;
5,356,552;
5,716,912;
5,849,676;
5,861,363 (alkyl and alkylene carbonates, e.g., ethylene carbonate);
5,328,622 (mono-epoxide);
5,026,495;
5,085,788;
5,259,906;
5,407,591 (poly (e.g., bis)-epoxides) and
4,686,054 (maleic anhydride or succinic anhydride). The foregoing list is not exhaustive and
other methods of capping nitrogen-containing dispersants are known to those skilled
in the art.
[0056] For adequate piston deposit control, a nitrogen-containing dispersant can be added
in an amount providing the lubricating oil composition with from about 0.03 mass %
to about 0.15 mass %, preferably from about 0.07 to about 0.12 mass %, of nitrogen.
[0057] Ashless dispersants are basic in nature and therefore have a TBN which, depending
on the nature of the polar group and whether or not the dispersant is borated or treated
with a capping agent, may be from about 5 to about 200 mg KOH/g. However, high levels
of basic dispersant nitrogen are known to have a deleterious effect on the fluoroelastomeric
materials conventionally used to form engine seals and, therefore, it is preferable
to use the minimum amount of dispersant necessary to provide piston deposit control,
and to use substantially no dispersant, or preferably no dispersant, having a TBN
of greater than 5. Preferably, the amount of dispersant employed will contribute no
more than 4, preferably no more than 3 mg KOH/g of TBN to the lubricating oil composition.
It is further preferable that dispersant provides no greater than 30, preferably no
greater than 25% of the TBN of the lubricating oil composition.
[0058] Additional additives may be incorporated in the compositions of the invention to
enable them to meet particular requirements. Examples of additives which may be included
in the lubricating oil compositions are metal rust inhibitors, viscosity index improvers,
corrosion inhibitors, oxidation inhibitors, friction modifiers, other dispersants,
anti-foaming agents, anti-wear agents and pour point depressants. Some are discussed
in further detail below.
[0059] Dihydrocarbyl dithiophosphate metal salts are frequently used as antiwear and antioxidant
agents. The metal may be an alkali or alkaline earth metal, or aluminum, lead, tin,
molybdenum, manganese, nickel or copper. The zinc salts are most commonly used in
lubricating oil in amounts of 0.1 to 10, preferably 0.2 to 2 wt. %, based upon the
total weight of the lubricating oil composition. They may be prepared in accordance
with known techniques by first forming a dihydrocarbyl dithiophosphoric acid (DDPA),
usually by reaction of one or more alcohol or a phenol with P
2S
5 and then neutralizing the formed DDPA with a zinc compound. For example, a dithiophosphoric
acid may be made by reacting mixtures of primary and secondary alcohols. Alternatively,
multiple dithiophosphoric acids can be prepared where the hydrocarbyl groups on one
are entirely secondary in character and the hydrocarbyl groups on the others are entirely
primary in character. To make the zinc salt, any basic or neutral zinc compound could
be used but the oxides, hydroxides and carbonates are most generally employed. Commercial
additives frequently contain an excess of zinc due to the use of an excess of the
basic zinc compound in the neutralization reaction.
[0060] The preferred zinc dihydrocarbyl dithiophosphates are oil soluble salts of dihydrocarbyl
dithiophosphoric acids and may be represented by the following formula:
wherein R and R' may be the same or different hydrocarbyl radicals containing from
1 to 18, preferably 2 to 12, carbon atoms and including radicals such as alkyl, alkenyl,
aryl, arylalkyl, alkaryl and cycloaliphatic radicals. Particularly preferred as R
and R' groups are alkyl groups of 2 to 8 carbon atoms. Thus, the radicals may, for
example, be ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, amyl, n-hexyl,
i-hexyl, n-octyl, decyl, dodecyl, octadecyl, 2-ethylhexyl, phenyl, butylphenyl, cyclohexyl,
methylcyclopentyl, propenyl, butenyl. In order to obtain oil solubility, the total
number of carbon atoms (i.e. R and R') in the dithiophosphoric acid will generally
be about 5 or greater. The zinc dihydrocarbyl dithiophosphate can therefore comprise
zinc dialkyl dithiophosphates. The present invention may be particularly useful when
used with lubricant compositions containing phosphorus levels of from about 0.02 to
about 0.12 mass %, such as from about 0.03 to about 0.10 mass %, or from about 0.05
to about 0.08 mass %, based on the total mass of the composition. In one preferred
embodiment, lubricating oil compositions of the present invention contain zinc dialkyl
dithiophosphate derived predominantly (e.g., over 50 mol. %, such as over 60 mol.
%) from secondary alcohols.
[0061] Oxidation inhibitors or antioxidants reduce the tendency of mineral oils to deteriorate
in service. Oxidative deterioration can be evidenced by sludge in the lubricant, varnish-like
deposits on the metal surfaces, and by viscosity growth. Such oxidation inhibitors
include hindered phenols, alkaline earth metal salts of alkylphenolthioesters having
preferably C
5 to C
12 alkyl side chains, calcium nonylphenol sulfide, oil soluble phenates and sulfurized
phenates, phosphosulfurized or sulfurized hydrocarbons, phosphorous esters, metal
thiocarbamates, oil soluble copper compounds as described in
U.S. Patent No. 4,867,890, and molybdenum-containing compounds.
[0062] Typical oil soluble aromatic amines having at least two aromatic groups attached
directly to one amine nitrogen contain from 6 to 16 carbon atoms. The amines may contain
more than two aromatic groups. Compounds having a total of at least three aromatic
groups in which two aromatic groups are linked by a covalent bond or by an atom or
group (e.g., an oxygen or sulfur atom, or a -CO-, -SO
2- or alkylene group) and two are directly attached to one amine nitrogen also considered
aromatic amines having at least two aromatic groups attached directly to the nitrogen.
The aromatic rings are typically substituted by one or more substituents selected
from alkyl, cycloalkyl, alkoxy, aryloxy, acyl, acylamino, hydroxy, and nitro groups.
[0063] Multiple antioxidants are commonly employed in combination. In one preferred embodiment,
lubricating oil compositions of the present invention contain from about 0.1 to about
1.2 mass % of aminic antioxidant and from about 0.1 to about 3 mass % of phenolic
antioxidant. In another preferred embodiment, lubricating oil compositions of the
present invention contain from about 0.1 to about 1.2 mass % of aminic antioxidant,
from about 0.1 to about 3 mass % of phenolic antioxidant and a molybdenum compound
in an amount providing the lubricating oil composition from about 10 to about 1000
ppm of molybdenum.
[0064] Representative examples of suitable viscosity modifiers are polyisobutylene, copolymers
of ethylene and propylene, polymethacrylates, methacrylate copolymers, copolymers
of an unsaturated dicarboxylic acid and a vinyl compound, interpolymers of styrene
and acrylic esters, and partially hydrogenated copolymers of styrene/ isoprene, styrene/butadiene,
and isoprene/butadiene, as well as the partially hydrogenated homopolymers of butadiene
and isoprene.
[0065] Friction modifiers and fuel economy agents that are compatible with the other ingredients
of the final oil may also be included. Examples of such materials include glyceryl
monoesters of higher fatty acids, for example, glyceryl mono-oleate; esters of long
chain polycarboxylic acids with diols, for example, the butane diol ester of a dimerized
unsaturated fatty acid; oxazoline compounds; and alkoxylated alkyl-substituted mono-amines,
diamines and alkyl ether amines, for example, ethoxylated tallow amine and ethoxylated
tallow ether amine.
[0066] Other known friction modifiers comprise oil-soluble organo-molybdenum compounds.
Such organo-molybdenum friction modifiers also provide antioxidant and antiwear credits
to a lubricating oil composition. Examples of such oil soluble organo-molybdenum compounds
include dithiocarbamates, dithiophosphates, dithiophosphinates, xanthates, thioxanthates,
sulfides, and the like, and mixtures thereof Particularly preferred are molybdenum
dithiocarbamates, dialkyldithiophosphates, alkyl xanthates and alkylthioxanthates.
[0067] Additionally, the molybdenum compound may be an acidic molybdenum compound. These
compounds will react with a basic nitrogen compound as measured by ASTM test D-664
or D-2896 titration procedure and are typically hexavalent. Included are molybdic
acid, ammonium molybdate, sodium molybdate, potassium molybdate, and other alkaline
metal molybdates and other molybdenum salts, e.g., hydrogen sodium molybdate, MoOCl
4, MoO
2Br
2, Mo
2O
3Cl
6, molybdenum trioxide or similar acidic molybdenum compounds.
[0068] Among the molybdenum compounds useful in the compositions of this invention are organo-molybdenum
compounds of the formulae:
Mo(ROCS
2)
4
and
Mo(RSCS
2)
4
wherein R is an organo group selected from the group consisting of alkyl, aryl, aralkyl
and alkoxyalkyl, generally of from 1 to 30 carbon atoms, and preferably 2 to 12 carbon
atoms and most preferably alkyl of 2 to 12 carbon atoms. Especially preferred are
the dialkyldithiocarbamates of molybdenum.
[0069] Another group of organo-molybdenum compounds useful in the lubricating compositions
of this invention are trinuclear molybdenum compounds, especially those of the formula
Mo
3S
kL
nQ
z and mixtures thereof wherein the L are independently selected ligands having organo
groups with a sufficient number of carbon atoms to render the compound soluble or
dispersible in the oil, n is from 1 to 4, k varies from 4 through 7, Q is selected
from the group of neutral electron donating compounds such as water, amines, alcohols,
phosphines, and ethers, and z ranges from 0 to 5 and includes non-stoichiometric values.
At least 21 total carbon atoms should be present among all the ligand organo groups,
such as at least 25, at least 30, or at least 35 carbon atoms.
[0070] A dispersant - viscosity index improver functions as both a viscosity index improver
and as a dispersant. Examples of dispersant - viscosity index improvers include reaction
products of amines, for example polyamines, with a hydrocarbyl-substituted mono-or
di-carboxylic acid in which the hydrocarbyl substituent comprises a chain of sufficient
length to impart viscosity index improving properties to the compounds. In general,
the viscosity index improver dispersant may be, for example, a polymer of a C
4 to C
24 unsaturated ester of vinyl alcohol or a C
3 to C
10 unsaturated mono-carboxylic acid or a C
4 to C
10 di-carboxylic acid with an unsaturated nitrogen-containing monomer having 4 to 20
carbon atoms; a polymer of a C
2 to C
20 olefin with an unsaturated C
3 to d
10 mono- or di-carboxylic acid neutralized with an amine, hydroxyl amine or an alcohol;
or a polymer of ethylene with a C
3 to C
20 olefin further reacted either by grafting a C
4 to C
20 unsaturated nitrogen-containing monomer thereon or by grafting an unsaturated acid
onto the polymer backbone and then reacting carboxylic acid groups of the grafted
acid with an amine, hydroxy amine or alcohol.
[0071] Pour point depressants, otherwise known as lube oil flow improvers (LOFI), lower
the minimum temperature at which the fluid will flow or can be poured. Such additives
are well known. Typical of those additives that improve the low temperature fluidity
of the fluid are C
8 to C
18 dialkyl fumarate/vinyl acetate copolymers, and polymethacrylates. Foam control can
be provided by an antifoamant of the polysiloxane type, for example, silicone oil
or polydimethyl siloxane.
[0072] Some of the above-mentioned additives can provide a multiplicity of effects; thus
for example, a single additive may act as a dispersant-oxidation inhibitor. This approach
is well known and need not be further elaborated herein.
[0073] In the present invention it may also be preferable to include an additive which maintains
the stability of the viscosity of the blend. Thus, although polar group-containing
additives achieve a suitably low viscosity in the pre-blending stage it has been observed
that some compositions increase in viscosity when stored for prolonged periods. Additives
which are effective in controlling this viscosity increase include the long chain
hydrocarbons functionalized by reaction with mono- or dicarboxylic acids or anhydrides
which are used in the preparation of the ashless dispersants as hereinbefore disclosed.
[0074] When lubricating compositions contain one or more of the above-mentioned additives,
each additive is typically blended into the base oil in an amount that enables the
additive to provide its desired function.
[0075] When lubricating compositions contain one or more of the above-mentioned additives,
each additive is typically blended into the base oil in an amount that enables the
additive to provide its desired function. Representative effect amounts of such additives,
when used in crankcase lubricants, are listed below. All the values listed are stated
as mass percent active ingredient.
Table II
ADDITIVE |
MASS % (Broad) |
MASS % (Preferred) |
Metal Detergents |
0.1-15 |
0.2 - 9 |
Corrosion Inhibitor |
0-5 |
0 - 1.5 |
Metal Dihydrocarbyl Dithiophosphate |
0.1 - 6 |
0.1 - 4 |
Antioxidant |
0 - 5 |
0.01 - 3 |
Pour Point Depressant |
0.01 - 5 |
0.01 - 1.5 |
Antifoaming Agent |
0 - 5 |
0.001 - 0.15 |
Supplemental Antiwear Agents |
0 - 1.0 |
0 - 0.5 |
Friction Modifier |
0 - 5 |
0 - 1.5 |
Viscosity Modifier |
0.01 - 10 |
0.25 - 3 |
Basestock |
Balance |
Balance |
[0076] Fully formulated lubricating oil compositions of the present invention preferably
have a TBN of at least 8.5, preferably at least 9, such as from about 8.5 to about
13, preferably from about 9 to about 13, and more preferably from about 9 to about
11 mg KOH/g (ASTM D-2896 and/or ASTM D-4739).
[0077] Fully formulated lubricating oil compositions of the present invention preferably
have a sulfated ash (SASH) content (ASTM D-874) of about 1.1 mass % or less, preferably
about 1.0 mass % or less, more preferably about 0.8 mass % or less.
[0078] Preferably, fully formulated lubricating oil compositions of the present invention
derive at least 5 %, preferably at least 10 %, more preferably at least 20 % of the
compositional TBN from ashless TBN sources including at least one compound of formula
(I). More preferably, fully formulated lubricating oil compositions of the present
invention derive at least 5 %, preferably at least 10 %, more preferably at least
20 % of the compositional TBN from at least one compound of formula (I), and less
than 25 %, preferably less than 20 %, more preferably less than 15 % of the compositional
TBN from ashless TBN sources other than compounds of formula (I), including basic
dispersants.
[0079] Fully formulated lubricating oil compositions of the present invention further preferably
have a sulfur content of less than about 0.4 mass %, more less than about 0.35 mass
% more preferably less than about 0.03 mass %, such as less than about 0.15 mass %.
Preferably, the Noack volatility (ASTM D5880) of the fully formulated lubricating
oil composition (oil of lubricating viscosity plus all additives and additive diluent)
will be no greater than 13, such as no greater than 12, preferably no greater than
10. Fully formulated lubricating oil compositions of the present invention preferably
have no greater than 1200 ppm of phosphorus, such as no greater than 1000 ppm of phosphorus,
or no greater than 800 ppm of phosphorus.
[0080] It may be desirable, although not essential to prepare one or more additive concentrates
comprising additives (concentrates sometimes being referred to as additive packages)
whereby several additives can be added simultaneously to the oil to form the lubricating
oil composition. A concentrate for the preparation of a lubricating oil composition
of the present invention may, for example, contain from about 5 to about 30 mass %
of one or more compounds of formula (I); about 10 to about 40 mass % of a nitrogen-containing
dispersant; about 2 to about 20 mass % of an aminic antioxidant, a phenolic antioxidant,
a molybdenum compound, or a mixture thereof; about 5 to 40 mass % of a detergent;
and from about 2 to about 20 mass % of a metal dihydrocarbyl dithiophosphate.
[0081] The final composition may employ from 5 to 25 mass %, preferably 5 to 18 mass %,
typically 10 to 15 mass % of the concentrate, the remainder being oil of lubricating
viscosity and viscosity modifier.
[0082] All weight (and mass) percents expressed herein (unless otherwise indicated) are
based on active ingredient (A.I.) content of the additive, and/or additive-package,
exclusive of any associated diluent. However, detergents are conventionally formed
in diluent oil, which is not removed from the product, and the TBN of a detergent
is conventionally provided for the active detergent in the associated diluent oil.
Therefore, weight (and mass) percents, when referring to detergents are (unless otherwise
indicated) total weight (or mass) percent of active ingredient and associated diluent
oil.
[0083] The invention will be further understood by reference to the following examples.
EXAMPLES
(i) Synthesis of 4-ethoxy-N-(4-methylpentan-2-yl)aniline
[0084] A 1 litre, three-necked round-bottomed flask equipped with a thermometer, addition
funnel and a mechanical stirrer was charged with 4-ethoxyaniline (20.00g, 143 mmol),
sodium triacetoxyborohydride (38.30g, 171 mmol) previously crushed in a mortar, and
475ml of dichloromethane. The addition funnel was charged with 4-methyl-2-pentanone
(15.98g, 157mmol) and 25ml of dichloromethane. The ketone was added slowly to the
flask via the funnel and the reaction left to proceed overnight. Following reaction,
saturated NaHCO
3 solution was added via the funnel. The organic phase was then washed again with saturated
NaHCO
3 solution, again with water and then dried using MgSO
4. After filtration and evaporation under vacuum, 31g of a pale yellow oil was obtained.
This product was used in the following step (ii).
(ii) Synthesis of 4-ethoxy-N-(2-ethylhexyl)-N-(4-methylpentan-2-yl)aniline
[0085] A 1 litre, three-necked round-bottomed flask equipped with a thermometer, addition
funnel and a mechanical stirrer was charged with 4-ethoxy-N-(4-methylpentan-2-yl)aniline
prepared in step (i) above (31.00g, 140 mmol), sodium triacetoxyborohydride (37.50g,
168 mmol) previously crushed in a mortar, and 475ml of dichloromethane. The addition
funnel was charged with 2-ethylhexanal (20.58g, 154mmol) and 25ml of dichloromethane.
The aldehyde was added slowly to the flask via the funnel and the reaction left to
proceed overnight. Following reaction, saturated NaHCO
3 solution was added via the funnel. The organic phase was then washed again with saturated
NaHCO
3 solution, again with water and then dried using MgSO
4. After filtration and evaporation under vacuum, 71.3g of a dark red oil was obtained.
This product was tested below where it is labelled as Synthesis Example 1.
Synthesis Example 2
(iii) Synthesis of 4-ethoxy-N-(butan-2-yl)aniline
[0086] A 2 litre, three-necked round-bottomed flask equipped with a thermometer, addition
funnel and a mechanical stirrer was charged with 4-ethoxyaniline (50.00g, 357 mmol),
sodium triacetoxyborohydride (104g, 464 mmol) previously crushed in a mortar, and
700ml of dichloromethane. The addition funnel was charged with 2-butanone (31.2g,
429mmol) and 50ml of dichloromethane. The ketone was added slowly to the flask via
the funnel and the reaction left to proceed for two days. The reaction was then quenched
by adding saturated NaHCO
3 solution via the funnel. The organic phase was then washed with saturated NaHCO
3 solution, again with water and then dried using MgSO
4. After filtration and evaporation under vacuum, 70.4g of a dark red oil was obtained.
This product was used in the following step (iii).
(iv) Synthesis of 4-ethoxy-N-(2-ethylhexyl)-N-(butan-2-yl)aniline
[0087] A 2 litre, three-necked round-bottomed flask equipped with a thermometer, addition
funnel and a mechanical stirrer was charged with 4-ethoxy-N-(butan-2-yl)aniline prepared
in step (iii) above (70.00g, 140 mmol), sodium triacetoxyborohydride (105g, 471 mmol)
previously crushed in a mortar, and 750ml of dichloromethane. The addition funnel
was charged with 2-ethylhexanal (58.0g, 435mmol) and 50ml of dichloromethane. The
aldehyde was added slowly to the flask via the funnel and the reaction left to proceed
for two days. The reaction was then quenched by adding saturated NaHCO
3 solution via the funnel. The organic phase was then washed with saturated NaHCO
3 solution, again with water and then dried using MgSO
4. After filtration and evaporation under vacuum, 108.2g of a dark red oil was obtained.
This product was tested below where it is labelled as Synthesis Example 2.
Comparative Example - (Synthesis Example 3)
[0088] 450 g of phenetidine (3.28 moles), 1682 g of 2-ethylhexanal (13.1 moles), 45 g of
10% Pd/C and 2L of dry methanol were charged into a Parr reactor. The reactor was
pressurized to 10 bar with hydrogen and stirred with heating to 100°C. The reaction
was monitored by HPLC to completion. The reactor was then cooled to room temperature
and the catalyst was removed by filtration. Distillation of the reaction mixture yielded
800g of product, the structure of which was confirmed by
1H- and
13C-NMR
[0089] The reaction scheme for the above-synthesis is shown below:
TBN Performance
[0090] The basicity of a lubricating oil composition can be determined by acid titration.
The resulting neutralization number is expressed as total base number, or TBN, and
can be measured using various methods. Method ASTM D-4739 (potentiometric hydrochloric
acid titration) was used herein. The ASTM D-4739 method is favoured in engine tests
and with used oils to measure TBN depletion/retention.
TBN Testing
[0091] A fully formulated lubricating oil composition containing dispersant, a detergent
mixture, antioxidant, ZDDP antiwear agent, pour point depressant and viscosity modifier,
in base oil was prepared. This lubricating oil composition, which was representative
of a commercial crankcase lubricant, was used as a reference lubricant. Fully formulated
lubricating oil compositions containing 1.68 mass% of the compounds of Synthesis Example
1 (Oil A) and Synthesis Example 2 (Oil B) were prepared. Also tested were fully formulated
lubricating oil compositions containing 1.00 mass % (Oil C) and 2.00 mass % (Oil D)
of the comparative compound of Synthesis Example 3. An additional amount of base oil
was added to each of the samples to provide comparable total mass. The TBN of each
of the resulting samples was determined in accordance with each of ASTM D4739 (in
units of mg KOH/g). The results are shown in Table III below.
Table III
Example |
Ref. |
Oil A |
Oil B |
Oil C |
Oil D |
Reference Sample (g) |
95.0 |
47.5 |
47.5 |
47.5 |
47.5 |
Added Base Oil (g) |
5.0 |
1.66 |
1.66 |
2 |
1.5 |
Aniline compound (g) |
- |
0.84 |
0.84 |
0.5 |
1.0 |
Total Weight (g) |
100 |
50 |
50 |
50 |
50 |
TBN by D-4739 |
8.75 |
10.49 |
11.60 |
8.87 |
8.97 |
ΔTBN against Ref. by D-4739 |
- |
1.74 |
2.85 |
0.12 |
0.22 |
[0092] As shown, the compounds of the invention as used in Oil A and Oil B effectively increased
the TBN of the lubricating oil composition as measured by ASTM D-4739, without contributing
to SASH content. The comparative compound of Synthesis Example 3 having a di-alkyl
branching arrangement not according to the present invention gave no significant improvement
in TBN. This was so even in the case of Oil D where a greater amount of compound was
used (2.00 mass% vs. 1.64 mass%).
Fluoroelastomer seal compatibility testing.
[0093] Oil A and a similar oil containing N,N-di-n-hexyl-4-ethoxyaniline in place of the
compound of the invention were tested in the VW-6/AK6 test. This procedure tests compatibility
of lubricating oils with Viton fluoroelastomer seal materials. The elongation at break
for a reference oil containing neither compound was on average -34.5% compared to
a new seal. For Oil A, the average was -51% and for the oil containing N,N-di-n-hexyl-4-ethoxyaniline,
-64%. These tests show that the compound of the invention had a much lower impact
on the seal material than the analogous compound bearing two liner alkyl chains.