[0001] This invention relates to fire resistant (difficultly inflammable) fluids based on
esters of phosphoric acid. More particularly, the invention relates to a fire resistant
fluid based on a phosphoric acid ester or a mixture of phosphoric acid esters and
containing a corrosion and hydrolysis inhibitor.
[0002] Hydraulic fluids based on phosphoric acid esters have been used for some time. They
have characteristics suitable therefor; particularly, they are not easily inflammable,
so that they are used above all in systems comprising closed hydraulic circuits such
as hydraulic systems of turbines and of pressure casting, continuous casting and press
plants. The use of such fluids is described for example in U.S. Patent 3,468,802 and
U.S. Patent 3,723,315.
[0003] Although such fluids are not easily inflammable and of relatively high thermal stability,
they may, in certain applications, possess insufficient resistance to oxidation and/or
hydrolysis or they may be highly corrosive to certain metals. To remedy such defects
of the known fluids certain inhibitors may be added thereto. For example, certain
aminopyridines may be added as antioxidants (U.S. Patent 3,783,132). Also, oxazolines
and imidazolines may be added as rust inhibitors (British Patent 1,317,636). Finally,
it is known to use certain amino compounds as corrosion inhibitors (U.S. Patent 3,468,802).
However, many of the proposed rust inhibitors show undesirable side effects which
impair the applicability of the hydraulic fluid.
[0004] In accordance with the invention there is provided a fire resistant fluid comprising
a phosphate ester and a corrosion or hydrolysis inhibiting amount of piperazine or
a substituted piperazine.
[0005] The fluid of the invention may be useful as a lubricant, a hydraulic fluid, a transformer
oil or for a variety of other purposes wherein a fire resistant fluid is required.
[0006] The problem underlying this invention is to develop a fire resistant fluid having
improved characteristics compared to those of known fluids used in hydraulic systems,
especially with regard to corrosion inhibition and/or hydrolytic stability.
[0007] This is achieved by a fire resistant fluid based on a phosphoric acid ester or a
mixture of phosphoric acid esters and containing piperazine and/or at least one piperazine
derivative as corrosion and/or hydrolysis inhibitor.
[0008] The use of such additives in phosphate esters confers not only improved hydrolytic
stability but also better corrosion inhibiting properties; particularly, the rust-preventing
properties are improved.
[0009] The proportion of piperazine or piperazine derivative in fluids according to the
invention is in the range of 0.005 to 5% by weight and is preferably in the range
of 0.01 to 0.5% by weight.
[0010] The phosphate esters used as the base for fire resistant fluids are mainly aryl esters
of phosphoric acid. The triaryl esters are particularly-preferred because they are
clearly superior in regard to fire resistance but diaryl alkyl phosphate esters may
also be employed. The preferred triaryl phosphate esters include, inter alia, tricresyl
phosphate ester, trixylyl phosphate ester, phenyl dicresyl phosphate ester, cresyl
diphenyl phosphate ester and tri(isopropylphenyl) phosphate ester, di(isopropylphenyl)
phenyl phosphate ester and isopropylphenyl diphenyl phosphate ester. Diphenyl-2-ethylhexyl
phosphate ester is an example of the diarylalkyl phosphate ester which may be used,
although with a clear loss of fire resistance in the fluid. If greater fire resistance
is required halogenated phosphate esters may be used, in particular chlorinated aryl
esters which, however, have considerable other disadvantages (such as corrosion).
[0011] The corrosion and hydrolysis inhibitor may be piperazine itself or a substituted
piperazine. Thus, alkyl, aryl, alkaryl and aralkyl substituted piperazines may be
used, and the substituent groups may themselves be substituted, for example, by halogene,
hydroxy, alkoxy, amino, alkylamino or dialkylamino groups. Other substituent groups
on the piperazine ring may be hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, alkoxyaryl,
amino, aminoalkyl, alkylamino, dialkylamino, alkylaminoalkyl and dialkylamino alkyl.
The substitution may be made on the carbon or nitrogen atoms of the piperazine ring.
Preferred types of substituted piperazine are:
Alkyl-, Dialkyl-, Trialkyl- or Tetraalkyl- piperazine,
N-alkyl-piperazine,
N,N'-Dialkyl-piperazine,
N-Aryl-piperazine,
N,N'-Diaryl-piperazine,
N-Alkylaryl-piperazine,
N,N-Di(Alkylaryl)-piperazine,
N-Hydroxyalkyl-piperazine,
N,N'-Di(hydroxyalkyl)-piperazine,
N-Aminoalkyl-piperazine, and
N,N'-Di(aminoalkyl)-piperazine.
[0012] In addition to piperazine and derivatives thereof the fluid according to the invention
may also include other additives when this is desirable for particular applications.
These other additives may be, for example, metal deactivators, antioxidants and antifoaming
agents.
[0013] Examples of antioxidants are:
Alkyl and non-alkylated aromatic amine:
Dioctyl-diphenylamine; tertiary octylphenyl-α
-naphthylamine; ditertiary octylpheno- thiazine; phenyl-α-naphthylamine; N,N'- di(sec
butyl)-p-phenylenediamine.
Sterically hindered phenols:
2,6-ditertiarybutyl-p-cresol; 2,6-di- tertiarybutylphenol; 2,4,6-triisopropyl- phenol;
2,2'-thio-bis-(4-methyl-6-tert butylphenol).
[0014] Esters of thiodipropionic acid: Dilaurylthiodipropionate ester.
[0015] Complex organic chelates: Copper-bis(trifluoracetyl acetonate), copper phthalocyanine,
tributyl ester of EDTA.
[0016] Examples of antifoaming agents are silicones.
EXAMPLE 1
EXAMPLE 2
[0018] The effect of the piperazine derivatives was tested with regard to hydrolytic stability
in accordance with the BBC Hydrolytic Stability Test (BBC ZLC 2-5-40, 100°C, 96 hours,
(no clay treatment). The results of the tests are as follows:

[0019] In Tables 1 and 2, Esters A-E are mixtures of the following:
Tri(isopropylphenyl) phosphate, di(isopropylphenyl) phenyl phosphate, isopropylphenyl
diphenyl phosphate and triphenyl phosphate.
1. A fluid comprising a phosphate ester and a corrosion or hydrolysis inhibiting amount
of piperazine or a substituted piperazine.
2. The fluid of Claim 1 wherein said phosphate ester is an aryl ester of phosphoric
acid.
3. The fluid of Claim 2 wherein the aryl ester is a diaryl ester.
4. The fluid of Claim 3 wherein the diaryl ester is diphenyl-2-ethylhexyl phosphate.
5. The fluid of Claim 2 wherein the aryl ester is a triaryl ester.
6. The fluid of Claim 5 wherein the triaryl est±r is selected from the group consisting
of tricresyl phosphate, trixylyl phosphate, phenyl dicresyl phosphate, cresyl diphenyl
phosphate, and tri(isopropylphenyl) phosphate.
7. The fluid of Claim 1 wherein the corrosion or hydrolysis inhibitor is piperazine.
8. The fluid of Claim 1 wherein the corrosion inhibitor is a substituted piperazine.
9. The fluid of Claim 8 wherein the substituent is selected from the group consisting
of alkyl, aryl, alkaryl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, alkoxyaryl, amino,
aminoalkyl, alkylamino, dialkylamino, alkylaminoalkyl and dialkylaminoalkyl.
10. The fluid of Claim 9 wherein said substituent is itself substituted with a member
selected from the group consisting of halogen, hydroxy, alkoxyl, amino, alkylamino
and dialkylamine.
11. The fluid of Claim 1 wherein the inhibitor is N,N'-dimethyl piperazine.
12. The fluid of Claim 1 wherein the inhibitor is 2-methyl piperazine.
13. The fluid of Claim 1 wherein the inhibitor is N-methyl piperazine.
14. The fluid of Claim 1 wherein the inhibitor is 1-(2-hydroxy) piperazine.
15. The fluid of Claim 1 wherein the inhibitor is N-(2-aminoethyl) piperazine.
16. The fluid of Claim 1 wherein the inhibitor is N-phenyl piperazine.
17. The fluid of Claim 1 wherein the inhibitor is N-benzyl piperazine.
18. The fluid of Claim 1 wherein the inhibitor is 2,5-dimethyl piperazine.