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| United States Patent | 4961868 |
| Link to this page | http://www.wikipatents.com/4961868.html |
| Inventor(s) | Doner; John P. (Sewell, NJ);
Horodysky; Andrew G. (Cherry Hill, NJ);
Keller, Jr.; John A. (Pitman, NJ) |
| Abstract | The invention is a grease composition comprising a major proportion of a
grease, a hydroxy-containing soap thickener and a minor amount of a
compound prepared by reacting a boron compound with an organic compound
containing oxygen, sulfur and/or nitrogen. Sulfur and/or phosphorous
compounds are also incorporated into the composition. |
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Title Information  |
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| Publication Date |
October 9, 1990 |
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| Filing Date |
March 7, 1989 |
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| Parent Case |
CROSS REFERENCE TO RELATED APPLICATIONS
This is a continuation of copending application Ser. No. 210,136 filed on
June 13, 1988, now abandoned, which is a continuation of copending
application Ser. No. 081,590 filed on Aug. 3, 1987, now abandoned, which
is a continuation of copending application Ser. No. 851,637 filed on Apr.
14, 1986, now abandoned which is a continuation-in-part of each of the
following copending applications, each of which, as well as the
application parent thereto, is incorporated herein by reference:
Application Ser. No. 774,873, filed Sept. 12, 1985, abandoned, which is a
continuation of application Ser. No. 641,077, filed Aug. 15, 1984
abandoned, which is a continuation-in-part of U.S. application Ser. No.
587,328, filed Mar. 7, 1984, abandoned.
U.S. application Ser. No. 641,078, filed Aug. 15, 1984, abandoned which is
a continuation-in-part of application Ser. No. 577,454, filed Feb. 6,
1984, abandoned.
U.S. application Ser. No. 831,073, filed Feb. 18, 1986, abandoned, which is
a continuation of Ser. No. 643,344, abandoned, filed Aug. 22, 1984.
U.S. application Ser. No. 643,346, filed Aug. 22, 1984, now U.S. Pat. No.
4,600,517.
U.S. application Ser. No. 792,168, filed Oct. 25, 1985, abandoned, which is
a continuation of application Ser. No. 643,347 filed Aug. 22, 1984
abandoned.
U.S. application Ser. No. 769,827, filed Aug. 27, 1985.
U.S. application Ser. No. 769,826, filed Aug. 27, 1985, U.S. Pat. No.
4,743,386 which is a continuation-in-part of application Ser. No. 682,579,
filed Dec. 17, 1984, abandoned, which is a continuation of application
Ser. No. 445,883, filed Dec. 1, 1982, abandoned U.S. Ser. No. 769,826 is a
continuation-in-part of application Ser. No. 638,609, filed Aug. 7, 1984,
U.S. Pat. No. 4,571,248 which is a division of application Ser. No.
456,880, filed Jan. 10, 1983, now U.S. Pat. No. 4,486,321.
U.S. application Ser. No. 769,912, filed Aug. 27, 1985, abandoned.
U.S. application Ser. No. 769,837, filed Aug. 27, 1985, U.S. Pat. No.
4,655,948.
U.S. application Ser. No. 641,079, filed Aug. 15, 1984, now U.S. Pat. No.
4,582,617, which is a continuation-in-part of U.S. application Ser. No.
519,878, filed Aug. 3, 1983, abandoned. |
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Title Information  |
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References  |
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| *references marked with an asterisk below are user-added references |
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U.S. References |
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|      Your vote accepted [0 after 0 votes] | | 4582617 Doner 508/185 Apr,1986 |      Your vote accepted [0 after 0 votes] | | 4529529 Horodysky 508/194 Jul,1985 |      Your vote accepted [0 after 0 votes] | | 4524005 Horodysky 508/194 Jun,1985 |      Your vote accepted [0 after 0 votes] | | 4486321 Horodysky 508/193 Dec,1984 |      Your vote accepted [0 after 0 votes] | | 4472289 Horodysky 508/199 Sep,1984 |      Your vote accepted [0 after 0 votes] | | 4440656 Horodysky 508/199 Apr,1984 |      Your vote accepted [0 after 0 votes] | | 4410438 Horodysky 508/185 Oct,1983 |      Your vote accepted [0 after 0 votes] | | 4406802 Horodysky 508/194 Sep,1983 |      Your vote accepted [0 after 0 votes] | | 4389322 Horodysky 508/194 Jun,1983 |      Your vote accepted [0 after 0 votes] | | 4382006 Horodysky 508/195 May,1983 |      Your vote accepted [0 after 0 votes] | | 4376712 Horodysky 508/198 Mar,1983 |      Your vote accepted [0 after 0 votes] | | 4374032 Gemmill 508/191 Feb,1983 |      Your vote accepted [0 after 0 votes] | | 4370248 Horodysky 508/198 Jan,1983 |      Your vote accepted [0 after 0 votes] | | 4159957 de Vries 508/195 Jul,1979 |      Your vote accepted [0 after 0 votes] | | 4140492 Feldman 44/317 Feb,1979 |      Your vote accepted [0 after 0 votes] | | 4016092 Andress 508/189 Apr,1977 |      Your vote accepted [0 after 0 votes] | | | | | |
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| Market Size |
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| Reasonable Royalty |
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Market Review  |
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Technical Review  |
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Claims  |
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We claim:
1. An improved grease composition comprising a major proportion of a
lubricating compound and:
(a) a borated derivative of an organic compound,
(b) a metal or amine derivative of a hydroxy-containing or
polyhydroxy-containing carboxylate soap thickener wherein said metal is
selected from calcium and lithium, and
(c) a phosphorus and sulfur containing compound selected from the group
consisting of zinc dihydrocarbyldithiophosphates; said borated organic
compound, said hydroxy-containing thickener and said phosphorus and sulfur
containing compound each being present in an amount sufficient to increase
the dropping point over the dropping point of a grease without said
borated organic compound and said phosphorus sulfur containing compound.
2. The composition of claim 1 wherein hydrocarbyl is selected from alkyl
and alkaryl groups having from about 3 to about 18 carbon atoms.
3. The composition of claim 2 wherein the hydrocarbyl group in an alkyl
group.
4. The composition of claim 3 wherein the alkyl group is derived from mixed
C.sub.3 secondary and C.sub.6 primary alcohols.
5. An improved grease composition comprising a major proportion of a
lubricating component and:
(a) means for elevating the dropping point of a grease comprising a
sufficient amount of a borated derivative of an organic compound; and
(b) a metal or amine derivative of a hydroxy-containing or
polyhydroxy-containing carboxylate soap thickener wherein said metal is
selected from lithium and calcium, and
(c) a phosphorus and sulfur containing compound selected from the group
consisting of zinc dihydrocarbyldithiophosphates.
6. The composition of claim 5 wherein said borated derivative is present in
said grease composition in an amount of between about 0.2 and about 10
percent by weight.
7. The composition of claim 5 wherein the total amount of thickener added
is between about 3 and about 20 percent by weight of the total
composition.
8. The composition of claim 7 wherein the thickener contains at least 15
percent by weight of hydroxy-containing thickener.
9. The composition of claim 5 wherein said grease contains between about
0.2 and about 10 percent by weight of said phosphorus- and sulfur-
containing compounds.
10. The composition of claim 5 wherein said hydroxy-containing soap
thickener is lithium hydroxystearate.
11. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting an alkoxylated alcohol of the formula
(RO)(R.sup.1 O).sub.x H
wherein R is a hydrocarbyl group or a mixture of hydrocarbyl groups,
containing from 1 to 50 carbon atoms, R.sup.1 is a C.sub.2 to C.sub.4
hydrocarbylene group and x is from 1 to 7 with a boron compound.
12. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting an alcohol of the formula
R.sup.2 OH
wherein R.sup.2 is a hydrocarbyl group, or mixture thereof, containing from
1 to 30 carbon atoms, with a boron compound.
13. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting a diol of the formula
R.sup.3 (OH).sub.2
wherein R.sup.3 is a hydrocarbyl group containing from 2 to 30 carbon atoms
with a boron compound.
14. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting an amine of the formula
##STR14##
wherein x is 0 to 2, R.sup.4, R.sup.5, R.sup.7 and R.sup.8 are hydrogen or
hydrocarbyl groups containing from 1 to 30 carbon atoms, hydroxyalkyl
groups containing 2 to 4 carbon atoms, a polyalkoxylated group containing
6 to 20 carbon atoms or th latter group containing sulfur or additional
oxygen, at least one of R.sup.4, R.sup.5, R.sup.7 and R.sup.8 being a
non-hydrogen group and R.sup.6 is a C.sub.2 to C.sub.4 alkylene group,
with a boron compound.
15. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting an ester of the formula
R.sup.9 (COOR.sup.10).sub.n
wherein n is 1 to 5 and R.sup.9 and R.sup.10 are hydrocarbyl or
hydroxyhydrocarbyl groups containing 1 to 20 carbon atoms, at least one of
R.sup.9 and R.sup.10 being a hydroxyhydrocarbyl group with a boron
compound.
16. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting an oxazoline of the generalized
structure
##STR15##
where R.sup.11 is a hydrocarbyl or hydrocarbylene group of one to fifty
carbon atoms, at least one of R.sup.12 or R.sup.13 is hydrogen and the
other is hydrogen or has the generalized structure
##STR16##
where R.sup.14 is hydrogen or a hydrocarbyl group of one to fifty carbon
atoms with a boron compound.
17. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting an oxazoline of the generalized
structure
##STR17##
where R.sup.17 is a hydrocarbyl or hydrocarbylene group of one to fifty
carbon atoms, at least one of R.sup.15 or R.sup.16 is hydrogen and the
other is hydrogen or has the generalized structure
##STR18##
where R.sup.18 is hydrogen or a hydrocarbyl group of one to fifty carbon
atoms with a boron compound.
18. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting an amine with an aldehyde and a phenol
or mercaptan and subsequently reacting the resulting product with a boron
compound, the hydroxy-containing thickener and borated amine condensation
product being present in sufficient quantities to effect an increase in
the dropping point of said grease.
19. The composition of claim 5 wherein the borated derivative is the
reaction product made by reacting an hydroxyl-containing amide having the
structural formula:
##STR19##
wherein R.sup.19 is a hydrocarbyl group of 1 to 60 carbon atoms and can
additionally contain sulfur, oxygen and/or nitrogen;
R.sup.20 and R.sup.21 are each a hydrocarbylene group or a mixture of
hydrocarbylene groups of 2 to 6 carbon atoms;
x is 0 to 15, and
y is 0 to 15, provided that x+y equals at least 1 with a boron compound.
20. The composition of claim 5 wherein the lubricating component is
selected from the group consisting of mineral oils, synthetic oils, or
mixtures thereof.
21. The composition of claim 20 wherein the synthetic oils are polglycols,
synthetic hydrocarbons, alkyl benzenes, dibasic acid esters, polyol
esters, phosphate esters or mixtures thereof.
22. The composition of claim 5 wherein the borated derivative additionally
contains oxygen, sulfur, and/or nitrogen which is reactive with a borating
agent.
23. The composition of claim 5 wherein the borated derivative of an organic
compound contains additionally any of the elements of the Periodic Table
of the Elements.
24. The composition of claim 5 wherein the borated derivative is a
polymeric organic borate.
25. A method for elevating the dropping point of a grease composition
comprising incorporating into said grease product means for elevating the
dropping point of said grease comprising an organic boron compound, a
metal or amine derivative of a hydroxy-containing or
polyhydroxy-containing soap carboxylate thickener wherein said metal is
selected from lithium and calcium and a phosphorus and sulfur containing
compound selected from the group consisting of zinc
dihydrocarbyldithiophosphates.
26. The method of claim 25 wherein the hydroxy-containing soap thickener is
at least 15% by weight of the total thickener is said grease composition.
27. The method of claim 25 wherein the borated derivative additionally
contains oxygen, sulfur and/or nitrogen which is reactive with a borating
agent.
28. The method of claim 25 wherein the borated derivative contains
additionally any of the elements of the Periodic Table of the Elements.
29. The method of claim 25 wherein the borated organic compound is a
polymeric organic borate.
30. A method for making grease wherein a liquid lubricant is mixed with a
thickening agent, the improvement comprising adding to said grease means
for elevating the dropping point of a grease comprising a borated organic
compound, a metal or amine derivative of a hydroxy-containing or
polyhydroxy-containing soap carboxylate thickener wherein said metal is
selected from lithium and calcium and a phosphorus and sulfur containing
compound selected from the group consisting of zinc
dihydrocarbyldithiophosphates.
31. The method of claim 30 wherein the borated derivative additionally
contains oxygen sulfur and/or nitrogen which is reactive with a borating
agent.
32. The method of claim 30 wherein the borated derivative contains
additionally any of the Periodic Table of the Elements.
33. The method of claim 30 wherein the borated organic compound is a
polymeric organic borate.
34. An improved grease composition comprising a major proportion of a
lubricating component and: comprising
(a) a borated derivative of an organic compound containing an hydroxyl,
epoxide, thiol or nitrogen moiety which is reactive with a borating agent,
and
(b) a metal or amine derivative of a hydroxy-containing or
polyhydroxy-containing carboxylate soap thickener wherein said metal is
selected from lithium and calcium, and
(c) a phosphorus and sulfur containing compound selected from the group
consisting of zinc dihydrocarbyldithiophosphates.
35. A method for elevating the dropping point of a grease composition
comprising incorporating into said grease means for elevating the dropping
point thereof; comprising an amount sufficient to significantly improve
the dropping point of
(a) a borated derivative of an organic compound containing an hydroxyl,
epoxide, thiol or nitrogen moiety,
(b) a metal or amine derivative of a hydroxy-containing or
polyhydroxy-containing carboxylate soap thickener wherein said metal is
selected from lithium and calcium, and
(c) a phosphorus and sulfur containing compound selected from the group
consisting of zinc dihydrocarbyldithiophosphates.
36. An improved grease composition comprising proportion of a component
and:
(a) means for elevating the dropping point of a grease comprising an amount
sufficient to significantly improve the dropping point of a borated
derivative of an organic compound containing an hydroxyl, epoxide, thiol
or nitrogen moiety which is reactive with a borating agent,
(b) a metal or amine derivative of a hydroxy-containing or
polyhydroxy-containing carboxylate soap thickener wherein said metal is
selected from lithium and calcium, and
(c) a phosphorus and sulfur containing compound selected from the group
consisting of zinc dihydrocarbyldithiophosphates. |
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Claims  |
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Description  |
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FIELD OF THE INVENTION
The invention is concerned with a novel group of grease compositions. It
more particularly relates to a grease composition comprising oil, a
thickener of which at least 10-15% of said thickener is a
hydroxy-containing soap thickener and borated derivative of an organic
compound containing optionally and preferably an oxygen, sulfur or
nitrogen moiety which is reactive with a borating agent, and said borated
derivation can optionally contain any other element of the Periodic Chart,
the grease compositions optionally containing additional phosphorus and
sulfur moieties.
DISCUSSION OF THE PRIOR ART
Borated alkoxylated alcohols have been used in commercial lubricant
formulations to provide improvement in lubricity properties. This is known
from U.S. Pat. No. 3,711,411, which discloses hydraulic fluids containing
such products.
It is known further than borated esters and related borates can be used in
other areas. For example, U.S. Pat. No. 3,740,358 teaches a
phenol-aldehyde foamable composition containing a boron compound, e.g. a
material formed by reacting boric acid or boric oxide with an aliphatic
hydroxyl-containing compound.
U.S. Pat. No. 2,160,917 discloses lubricants containing low molecular
weight borate esters, e.g., borate esters containing from 4 to 12 carbon
atoms. The disclosed borates include the tributyl and trilauryl borates.
Other patents include U.S. Pat. No. 3,014,870 (to mixtures of amine and
certain boronic mono- or diesters); U.S. Pat. No. 3,108,966 (aryl boronic
esters and thio acid ester lubricants); U.S. Pat. No. 3,133,951 (fuels
containing dialkyl boron esters); U.S. Pat. No. 3,347,793 (teriaryalkyl
boron esters) and U.S. Pat. No. 3,509,054 (esters or boron acids with
2,6-dialkyl-phenols).
From U.S. Pat. No. 4,328,113 it is also known that borated amines, such as
borated hydrocarbyl mono-and diamines, are useful as friction reducers in
lubricants, especially in lubricating oils.
Vicinal hydroxyl-containing alkyl carboxylates such as glycerol monooleate
have found use as lubricity additives. U.S. Pat. No. 2,788,326 discloses
some of the esters suitable for the present invention, e.g., glycerol
monooleate, as minor components of lubricating oil compositions, U.S. Pat.
No. 3,233,498 discloses, among others, the same ester as just mentioned,
as an additive to other oils. U.S. Pat. No. 2,443,578 teaches esters
wherein the free hydroxyl is found in the acid portion, as for example, in
tartaric acid.
The above patents, as are numerous others, are directed to the use of such
esters as additives. Other patents, such as U.S. Pat. Nos. 2,798,083;
2,820,014; 3,115,519; 3,282,917 and 3,309,318 as well as an article by R.
R. Barnes et al. entitled "Synthetic Ester Lubricants" in Lubrication
Engineering, August, 1975, pp. 454-457, teach lubricants prepared by
polyhydric alcohols and acid containing no hydroxyl other than those
associated with the acid function.
U.S. Pat. No. 4,374,032 corresponding to application Ser. No. 134,849,
filed Mar. 28, 1980, discloses the use of borated adducts of oxazolines as
a component of lubricating oils. U.S. Pat. No. 4,374,032 is incorporated
herein by reference.
U.S. Pat. No. 4389,322 discloses the use of borated adducts of ethoxylated
amides as a component of lubricating oils or greases. U.S. Pat. No.
4,389,322 is incorporated herein by reference.
The borated adducts of ethoxylated amides are prepared from ethoxylated
compounds having the following generalized structure:
##STR1##
R is a hydrocarbyl group having from about 1 to about 60 (preferably 8 to
30) carbon atoms; R may be alkyl, alkenyl, aralkyl, alkylaryl, etc; x and
y may be the same or different and are each a whole number from 0 to about
15, preferably 1 to 5, but the sum of x and y must equal 1 or more, or
more preferably, 2 or more. R.sup.4 is hydrogen or an alkyl or alkenyl
radical of one to six carbon atoms and preferably is hydrogen or a methyl
radical.
The borated derivatives can be prepared according to the discloses in U.S.
Pat. No. 4,490,256 which is incorporated herein by reference or by
treating the described amides with boric acid optionally in alcoholic
solvents such as butanol or pentanol, or optionally hydrocarbon solvents
such as benzene, toluene, xylene or mixtures thereof. Reaction
temperatures of 70.degree. to 260.degree. C. can be used but 110.degree.
to 170.degree. C. is preferred. Reaction times can be 1 to 10 hours or
more. Up to a stoichiometric amount or an excess of boric acid can be used
to produce a derivative containing 0.05% to 8% or more by weight of boron.
Other methods are also available to make similar borated derivatives. For
example, the ethoxylated amides may also be borated through
transesterification with a trialkyl borate such as tributyl borate (often
in the presence of boric acid).
The publication "Manufacture and Application of Lubricating Grease by C. J.
Boner (Reinhold Publishing Company) 1954, pp. 155 and 436, 437 disclose
the use of lithium soaps in grease making. The publication "Lubricant
Additive" by C. V. Smalheer et al. (Leyuis-Hiles Co.) 1967, pp. 1-11,
discloses the use of phosphonates and thiophosphonates as additives in
lubricants. "Condensed Chemical Dictionary" 9th Edition, (Van Nostrand
Reinhold Company) at pages 520 and 938 discloses the use of lithium
hydroxystearate in grease making and zinc dialkyldithiophosphate as a lube
oil additive.
These references, the publications by Boner and by Smalheer et al., and the
"Condensed Chemical Dictionary" refere | | |