Background
[0001] This invention relates generally to cyclic thioureas useful as additives for lubricating
oils.
[0002] Zinc dialkyldithiophosphates (ZDDP) are widely used as lubricant additives. The principal
disadvantages of these compounds are that an ash residue is produced by the zinc as
the additive is consumed, and that phosphorus is known to affect the efficiency of
catalytic converters in motor vehicles, thereby causing emissions problems. Cyclic
thiourea compounds useful as lubricant additives are disclosed in U.S. Patent No.
5,935,913. However, the compounds disclosed therein are not within the scope of the
present invention.
[0003] The problem addressed by this invention is to find additional non-metallic, non-phosphorus-containing
oil-soluble additives for lubricating oils.
Statement of Invention
[0004] The present invention is directed to a composition comprising:
(a) from 0.1% to 20% of at least one cyclic thiourea compound of formula I:

wherein W is O or S; R1 and R2 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl; R3 and R4 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl, or R3 and R4 groups combine with ring carbon atoms to which they are attached to form a five-
to seven-membered heterocyclic ring; and
(b) a lubricating oil.
[0005] The present invention is further directed to a method for improving the anti-wear
characteristics of a lubricating oil by adding from 0.1% to 20% of a compound of formula
I.
Detailed Description
[0006] All percentages are weight percentages based on the entire composition described,
unless specified otherwise. An "alkyl" group is a saturated hydrocarbyl group having
from one to twenty-two carbon atoms in a linear, branched or cyclic arrangement, and
having from 0 to 2 oxygen, nitrogen or sulfur atoms. Substitution on alkyl groups
of one or more halo, hydroxy, alkoxy, alkanoyl or amido groups is permitted; alkoxy,
alkanoyl and amido groups may in turn be substituted by one or more halo substituents.
In one preferred embodiment, alkyl groups contain from one to twelve carbon atoms
and from 0 to 1 oxygen, nitrogen or sulfur atoms; in another preferred embodiment,
alkyl groups contain from 12 to 22 carbon atoms, and more preferably, no heteroatoms.
An "alkenyl" group is an "alkyl" group in which at least one single bond has been
replaced with a double bond. An "aryl" group is a substituent derived from an aromatic
compound, including heterocyclic aromatic compounds having heteroatoms chosen from
among nitrogen, oxygen and sulfur. An aryl group has a total of from five to twenty
ring atoms, and has one or more rings which are separate or fused. Substitution on
aryl groups of one or more halo, alkyl, alkenyl, hydroxy, alkoxy, alkanoyl or amido
groups is permitted, with substitution by one or more halo groups being possible on
alkyl, alkenyl, alkoxy, alkanoyl or amido groups. An "aralkyl" group is an "alkyl"
group substituted by an "aryl" group. A "lubricating oil" is a natural or synthetic
oil, or a mixture thereof, having suitable viscosity for use as a lubricant, e.g.,
as crankcase oil in an internal combustion engine, automatic transmission fluid, turbine
lubricant, gear lubricant, compressor lubricant, metal-working lubricant, hydraulic
fluid, etc.
[0007] In one embodiment of the invention, preferably formula (I) has R
1, R
2, R
3 and R
4 which independently are hydrogen, alkyl, alkenyl, aryl or aralkyl, i.e., the compound
is not bicyclic. Preferably, R
1, R
2, R
3 and R
4 independently are hydrogen, alkyl or alkenyl, more preferably at least one of R
1, R
2, R
3 and R
4 is C
6-C
22 alkyl or alkenyl, more preferably at least one of R
1, R
2, R
3 and R
4 is C
10-C
22 alkyl, and most preferably at least one of R
1, R
2, R
3 and R
4 is C
16-C
22 alkyl.
[0008] In another embodiment of the invention R
3 and R
4 groups in formula I combine with ring carbon atoms to which they are attached to
form a five- to seven-membered heterocyclic ring. In a preferred embodiment R
3 and R
4 groups combine to form the following bicyclic system of formula (II):

wherein R
5 and R
6 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl. In a preferred embodiment
of the invention, in which W is O, R
1 and R
6 are the same, and R
2 and R
5 are the same, the compound is a symmetric bicyclic compound of formula (III):

[0009] In one embodiment of the invention, a compound of formula (I) is prepared from a
2-amino alkyl nitrile and carbon disulfide, as shown below:

Preferably, R
2 is C
6-C
22 alkyl or alkenyl, more preferably C
10-C
22 alkyl, and most preferably C
16-C
22 alkyl. Preferably, R
2 is derived from an unsubstituted C
16-C
22 alkyl amine, R
2NH
2, preferably one which is an oil-soluble amine. In one preferred embodiment, the alkyl
amine is a tertiary alkyl primary amine., i.e., a primary amine in which the alkyl
group is attached to the amino group through a tertiary carbon. Examples of commercially
available tertiary alkyl primary amines are the Primene
TM amines available from Rohm and Haas Company, Philadelphia, PA.
[0010] In one embodiment of the invention, a compound of formula (III) is prepared from
a substituted thiourea and a di-ester of acetylenedicarboxylic acid, as shown below:

The R groups are alkyl, alkenyl, or aralkyl groups, preferably C
1-C
4 alkyl groups. Preferably, R
1 and R
2 are hydrogen, alkyl or alkenyl, more preferably at least one of R
1 and R
2 is C
6-C
22 alkyl or alkenyl, more preferably at least one of R
1 and R
2 is C
10-C
22 alkyl, and most preferably at least one of R
1 and R
2 is C
16-C
22 alkyl.
[0011] In one embodiment of the invention, a compound of formula (I) is prepared from a
substituted thiourea and an ester of a α,β-unsaturated carboxylic acid, as shown below:

Preferably, R
3 and R
4 are hydrogen or C
1-C
4 alkyl. Preferably, R
1 and R
2 are hydrogen, alkyl or alkenyl, more preferably at least one of R
1 and R
2 is C
6-C
22 alkyl or alkenyl, more preferably at least one of R
1 and R
2 is C
10-C
22 alkyl, and most preferably at least one of R
1 and R
2 is C
16-C
22 alkyl.
[0012] Preferably, the compound(s) of formula (I) is present in a lubricating oil in a total
amount of at least 0.2%, more preferably at least 0.3%, and most preferably at least
0.4%. Preferably, the compound(s) of formula (I) is present in a lubricating oil in
a total amount no greater than 10%, more preferably no greater than 5%, and most preferably
no greater than 2%. Preferably, the compounds are soluble at the aforementioned levels.
[0013] Optionally, other additives typically used in lubricating oils are present in the
composition. Such additives include, but are not limited to, other anti-wear additives,
anti-corrosion additives, dispersants, detergents, antioxidants, antifoamants, friction
modifiers, seal swell agents, demulsifiers, viscosity index improvers and pour point
depressants. Other anti-wear additives that can be used in combination with the compound
of formula (I) include the commercial products known as ZDDP, which are zinc dialkyldithiophosphates.
In addition to improving the anti-wear characteristics of lubricating oils, the compound
of formula (I) typically also improves anti-corrosion characteristics and functions
as an anti-oxidant.
1. A composition comprising:
(a) from 0.1% to 20% of at least one cyclic thiourea compound of formula I:

wherein W is O or S; R1 and R2 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl; R3 and R4 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl, or R3 and R4 groups combine with ring carbon atoms to which they are attached to form a five-
to seven-membered heterocyclic ring; and
(b) a lubricating oil.
2. The composition of claim 1 in which W is O, and R1, R2, R3 and R4 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl.
3. The composition of claim 2 in which R1, R2, R3 and R4 independently are hydrogen or alkyl.
4. The composition of claim 3 in which at least one of R1, R2, R3 and R4 is C6-C22 alkyl.
5. The composition of claim 1 in which W is S, and R1, R2, R3 and R4 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl.
6. The composition of claim 1 in which R3 and R4 groups combine with ring carbon atoms to which they are attached to form a five-
to seven-membered heterocyclic ring.
7. The composition of claim 6 in which the cyclic thiourea has formula

wherein R
5 and R
6 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl.
8. The composition of claim 7 in which W is O, R1 and R6 are the same, and R2 and R5 are the same.
9. The composition of claim 8 in which R1 and R2 independently are hydrogen or alkyl.
10. The composition of claim 9 in which at least one of R1 and R2 is C6-C22 alkyl.