[0001] This invention relates to water-based hydraulic fluids thickened with water-soluble
polymers characterized by improved viscosity.
[0002] In the technology of hydraulic power transmission, mechanical power is imparted to
a fluid called "a hydraulic fluid" in the form of pressure by means of a hydraulic
pump. Power is utilized where desired by tapping a source of said hydraulic fluid
thus transforming the power as pressure back to mechanical motion by a mechanism called
a hydraulic motor. The hydraulic fluid is utilized as a pressure and volume transmitting
medium. Any non-compressible fluid can perform this function. Water is the oldest
fluid used for this purpose and is still sometimes used alone for this purpose. In
the prior art, there has been a heavy emphasis on the development of petroleum oils
for use as hydraulic fluids and, consequently, much of the equipment utilized.with
hydraulic fluids has been designed and manufactured specifically for use with petroleum
oils. A petroleum oil in comparison with water as a hydraulic fluid possesses the
advantage of inhibiting the development of rust of the ferrous components of the mechanical
equipment utilized in conjunction with hydraulic fluids, (i.e., hydraulic pumps, motors,
etc.) and in preventing wear of the machinery since the hydraulic fluid must lubricate
the equipment. Petroleum oils have a second advantage over the use of water as a hydraulic
fluid in that the petroleum oils normally exhibit a substantially higher viscosity
than water and thus contribute to reduction of the leakage of the fluid in the mechanical
equipment utilized. In addition, the technology relating to additives for petroleum
oils has developed to such an extent that the viscosity, foam stability, wear prevention
and corrosion prevention properties of such petroleum oil-based hydraulic fluids can
be further enhanced by the use of said additives.
[0003] Over the past 25 years, various substitutes for petroleum oil-based hydraulic fluids
have been developed in order to overcome one of the major deficiencies of petroleum
oils, namely, flammability. Recent interest in the use of hydraulic fluids having
up to 99 percent or more of water has resulted from the higher cost of petroleum oils
and recent emphasis on problems of ecologically suitable disposal of contaminated
or spent petroleum oil-based hydraulic fluids.
[0004] Mtalworking fluids of the so-called "soluble oil
* type have been considered for use as hydraulic fluids. Such fluids contain mineral
oil and emulsifiers as well as various additives to increase corrosion resistance
and improve antiwear and defoaming properties. Such fluids, when used as hydraulic
fluids, are not generally suitable for use in ordiry industrial equipment designed
specifically for use with the petroleum oil-based hydraulic fluids since such fluids
do not adequately prevent wear damage in some types of pumps and valves of such equipment.
However, such fluids have found application in specially designed, high cost, large
size equipment which, because of said large size and thus inflexibility, is not suitable
for use in most industrial plants. The soluble oil hydraulic fluid usage has thus
been quite limited; usage has been largely confined to large installations where flexibility
and size are not critical, such as in steel mills.
[0005] It is also known to use, in equipment designed for use in mineral oil-based hydraulic
fluids, flame-resistant: . glycol-water based hydraulic fluids such as are disclosed
in U.S. Patent No. 2,947,699. Up until recently, water-based hydraulic fluids containing
about 70 to 99+ percent water, have had very poor lubricating characteristics. While
hydraulic fluids are used primarily to transmit forces, it is necessary that they
provide lubrication for the impeller, rings, vanes, gears, pistons and cylinders and
other mechanical parts of hydraulic pumps in such systems in order to prevent excessive
wear on such parts.
[0006] Many prior art fluids, such as the petroleum oil type, are highly flammable and unsuitable
for certain uses where such fluids have frequently been the source of fire. Where
these fluids are used to control such industrial operations as heavy casting machines,
which are operated largely by hydraulic means, danger of fire exists. Therefore, there
is a growing demand for hydraulic fluids characterized by reduced flammability.
[0007] Hydraulic fluid compositions having water as a base are disclosed in U.S. Patents
Nos. 4,151,099 and 4,138,346. These patents disclose fluids comprising 1) a sulfur
containing compound and 2) a phosphate ester salt. The U.S. 4,151,099 patent also
includes a water-soluble polyoxyethylated ester of an aliphatic acid and a monohydric
or polyhydric aliphatic alcohol, either one or both said acid and said alcohol being
polyoxyethylated. These hydraulic fluids are optionally thickened with a polyglycol
thickener.
[0008] In U.S 2,558,030 a hydraulic fluid is disclosed having an organic polymeric thickener
such as copolymers of ethylene oxide and propylene oxide having high molecular weight.
[0009] U.S. 2,602,780 discloses hydraulic fluids with soluble polymeric thickeners such
as copolymers of ethylene oxide and propylene oxide having molecular weights of 15,000
to 20,000.
[0010] From the above it can be seen that it is well known in the art to employ in hydraulic
fluids organic polymeric thickeners such as copolymers of ethylene oxide and propylene
oxide having high molecular weight.

[0011] U.S. 3,346,501 discloses hydraulic fluids containing a conventional polyoxyalkylene
thickener, i.e., copolymers of ethylene oxide and 1,2-propylene oxide having molecular
weights of about 10,000 to 25,000 along with lauric acid and capric acid as antifoaming
agents in a conventional aqueous hydraulic fluid.
[0012] U.S. 3,580,847 discloses hydraulic fluid compositions employing high molecular weight
polyoxyalkylene polymers as thickeners along with acids such as lauric. This patent
calls for a two-phase hydraulic fluid with one. phase floating on the other, the floating
phase being a mineral oil or something similar.
[0013] U.S. 3,657,133 discloses a functional fluid such as transmission fluid which includes
acids such as lauric acid in combination with polyoxyalkylene glycols.
[0014] U.S. 3,629,111 discloses hydraulic fluids containing polyoxyalkylene glycols along
with capric and lauric acids. This patent is directed to use of a novel inhibitor
composition comprising a hydrazine compound with the organic acid.
[0015] This invention relates to thickened water-based hydraulic fluids. Such fluids are
prepared by blending water, organic thickener and conventional hydraulic fluid additives.
In accordance with the instant invention, it has been discovered that a substantial
increase in viscosity of a hydraulic fluid. thickened with a specified type of thickener
is achieved by blending with the fluid a very small amount of a carboxylic acid having
about 5 to 20 carbon atoms. The addition of a carboxylic acid has been found to substantially
increase the viscosity of a hydraulic fluid employing a thickener obtained by modifying
a conventional polyether polyol thickening agent with an alpha-olefin epoxide or glycidyl
ether having about 10 to 22 carbon atoms or mixtures thereof. Small amounts of higher
molecular weight glycols may also be incorporated into the chain. The hydraulic fluid
may be prepared by first preparing a concentrate containing from about 0 to 85 percent
by weight of water which is a most convenient form for shipping and which after shipping
is then further diluted with about 25 to 99 percent by weight water. The preparation
and shipping of such concentrates is preferred for high water type fluids. However,
water glycol type fluids are preferably prepared and shipped in the final or ready
to use form.
[0016] The above carboxylic acids which are added to increase viscosity in combination with
the specified thickener may be added to the thickener, the concentrate or to a finally
prepared hydraulic fluid.
[0017] In accordance with the instant invention the thickener is obtained by modifying a
conventional polyether polyol thickening agent with an alpha-olefin epoxide having
about 10 to 22 carbon atoms or mixtures thereof. Actually, any epoxide with a molecular
weight of about 150 to 300 may be employed. Any alcohol or aliphatic (or possibly
even aromatic) group of 10 to 24 carbons that can be placed at the end of the polyol
chain may be employed in lieu of the alpha-olefin epoxide. Glycidyl ethers make excellent
caps. A little ethylene oxide, propylene oxide or butylene oxide beyond the cap may
be employed. Small amounts of higher molecular weight glycols may be incorporated
into th4 chain. The conventional polyether polyol thickening agent can be an ethylene
oxide homopolymer or a straight or branched chain heteric or block copolymer of ethylene
oxide and at least one lower alkylene oxide having 3 to 4 carbon atoms. Said ethylene
oxide is used in the proportion of at least about 60 percent by weight based upon
the total weight of the polyether polyol. Generally, about 70 to 100 percent by weight
ethylene oxide is utilized with about 30 to 0 percent by weight of lower alkylene
oxide having 3 to 4 carbon atoms.
[0018] Such polyether polyols are generally prepared by reacting an active hydrogen-containing
compound having 1,2,3 or more active hydrogens with the ethylene oxide or ethylene
oxide and said lower alkylene oxide in the presence of an acid or basic oxyalkylation
catalyst and an inert organic solvent at elevated temperatures in the range of about
50°C to 150°C under an inert gas pressure generally from about 20 to about 100 pounds
per square inch gauge. Polyether polyols suitable as thickeners can be prepared by
further reacting a conventional polyether polyol as described above having a molecular
weight of about 1000 to about 40,000, preferably 2000 to about 30,000 with the above-described
epoxides, alcohols, glycidyl ethers, etc., so as to provide a cap on the polyether
polyol. The amount of epoxide, alcohol, glycidyl ethers, etc., required to obtain
the modified polyether polyol thickening agents of the invention is about 1 to about
20 percent by weight based upon the total weight of the modified polyether polyol
thickeners. Alternatively, the modified polyether polyol thickening agents can be
obtained by the copolymerization of a mixture of ethylene oxide and at least one other
lower alkylene oxide having 3 to 4 carbon atoms with an alpha-olefin epoxide having
about 12 to 18 carbon atoms or mixtures thereof. Further details of the preparation
of the alpha-olefin epoxide modified polyether polyol thickening agents useful in
the preparation of the hydraulic fluids of the invention can be obtained from co-pending
applications Serial No. 86,837 filed on October 22, 1979 and Serial No. 86,840 filed
October 22, 1979, both incorporated herein by reference.
[0019] Generally, about 10 to 60 percent of such thickeners based on the weight of the concentrate,
or 1 to 20 percent based on the weight of the final hydraulic fluid is employed.
[0020] In order to substantially increase viscosity in a hydraulic fluid employing the above-described
thickener, a carboxylic acid having 5 to 20 carbon atoms per COOH group and mixtures
thereof are blended with said fluid.
[0021] Preferred carboxylic acids for increasing viscosity in the presence of the above-described
thickener are lauric acid, capric acid, neodecanoic acid, stearic acid, palmitic acid,
oleic acid, sebacic acid, 4-octylbenzoic acid and adducts of organic acids.
[0022] While decanoic, also known as capric, acid has been well known in the art for years,
the neoacids, which are synthetic highly-branched organic acids, are relatively new.
The "neo" structure is generally considered to be as follows:

[0023] This product is described in the article entitled "Neoacids: Synthetic Highly Branched
Organic Acids", Journal of American Oil Chemists Society, Vol. 55, No. 4, pp. 342A
to 345A (1978).
[0024] Each of the above carboxylic acids may be used singly or in combination with one
or more of the other carboxylic acids set forth above. Generally the total amount
of said carboxylic acids would range from about 0.1 to 2 percent by weight in the
final hydraulic fluid. Where a concentrate is prepared first, the amount of said compounds
would be about 0.5 to 20 percent based on the weight of the concentrate.
[0025] The carboxylic acids described above may be employed with any conventional hydraulic
fluid incorporating any or all of the following prior art components. For example,
the hydraulic fluid may contain one or more of teh. following, as disclosed in U.S.
Patents Nos. 4,151,099 and 4,138,346; a phosphate ester, a sulfur compound, a water-soluble
polyoxyethylated aliphatic ester or ether and an alkyldialkanolamide. The fluid may
be a high water fluid or a water-glycol type fluid. Optionally, the fluids of the
invention can include a corrosion inhibitor, a defoamer and a metal deactivator (chelating
agent) as well as other conventional additives, such as dyes in normal amounts.
[0026] The phosphate ester may be selected from the group consisting of

and mixtures thereof wherein ethylene oxide groups are represented by EO; R is selected
from the group consisting of linear or branched chain alkyl groups wherein said alkyl
groups have about 6 to 30 carbon atoms, preferably about 8 to 20 carbon atoms, or
alkylaryl groups wherein the alkyl groups have about 6 to 30 carbon atoms, preferably
about 8 to 18 carbon atoms, and X preferably is selected from the group consisting
of hydrogen, alkali or alkaline earth metal, the residue of ammonia or an amine and
mixtures thereof, and n is a number from 1 to 50. Metals such as lithium, sodium,
potassium, rubidium, cesium, calcium, strontium, and barium are examples of the alkali
or alkaline earth metal..
[0027] The free acid form of the phosphate ester is preferably utilized in preparing hydraulic
fluids in accordance with compositions of the invention. These are more fully disclosed
in U.S. Patent 3,004,056 and U.S. 3,004,057, incorporated herein by reference. The
free acid 'form may be converted to the salt form in situ in the preparation of the
hydraulic fluids of the invention. Alternatively, the phosphate ester salts can be
used directly.
[0028] Water-soluble esters of ethoxylated aliphatic acids and/or water soluble ethers of
ethoxylated alcohols may be incorporated in the hydraulic fluid as an anti-wear lubricant
component. Preferred water-soluble esters or ethers are those of the ethoxylated CS-C36
aliphatic monohydric or polyhdyric alcohols or aliphatic acids, and aliphatic dimer
acids. The most desirable adducts are in the range of 10 to 20 carbons. Suitable esters
of ethoxylated aliphatic acids or alcohols are disclosed in U.S. Patent 4,151,099
particularly beginning in column 3 thereof which is hereby incorporated by reference.
[0029] Representative water-soluble polyoxyethylated esters having about 5 to about 20 moles
of oxide per mole are the polyoxyethylene derivatives of the following esters; sorbitan
monooleate, sorbitan trioleate, sorbitan monostearate, sorbitan tristearate, sorbitan
monopalmitate, sorbitan monoisostearate, and sorbitan monolaurate. ''
[0030] Conventional sulfur compound additives may also be incorporated in the hydraulic
fluid such as the ammonia, amine or metal salts of 2-mercaptobenzothiazole or 5-,
6-and 7-substituted 2-mercaptobenzothiazole, said salts being formed on neutralization
of the free acid form of 2-mercaptobenzothiazole with a base. Such sulfur compounds
are disclosed particularly beginning in column 5 of U.S. Patent 4,138,346 which is
hereby incorporated by reference.
[0031] The sulfur-containing compound may also be sulfurized oxymolybdenum and oxyantimony
compounds represented by:

wherein M is molybdenum or antimony and R is organic and is selected from the group
consisting of C
3-C
20 alkyl, aryl, alkylaryl radicals and mixtures thereof.
[0032] Representative useful molybdenum and antimony compounds are sulfurized oxymolybdenum
or oxyantimony organo-phosphorodithioate where the organic portion is alkyl, aryl
or alkylaryl and wherein said alkyl has a chain length of 3 to 20 carbon atoms.
[0033] The preferred alkyldialkanolamide has the formula

wherein R
1 is alkyl of about 4 to about 54, preferably about .4 to about 30, carbon atoms and
R
2 is alkyl of about 2 to .about 6 carbon atoms.
[0034] The alkyldialkanolamides are known compositions in the prior art. In general, these
compositions are prepared by esterifying a dialkanolamine with an alkyl dicarboxylic
acid and removing water of esterification. Useful alkyl dicarboxylic acids include
branched or straight chain saturated or unsaturated aliphatic monocarboxylic or dicarboxylic
acids as described below. Preferably, the saturated straight chain acids are used
and the preferred amides are diethanolamides. Examples of useful alkyldialkanolamides
are the alkyl diethanolamides and alkyl dipropanol amides where the alkyl group is
derived from a C
8-C
54 dicarboxylic acid.
[0035] The advantageous properties contributed to the hydraulic fluid by the alkyldialkanolamide
component of the hydraulic fluid of the invention are resistance to precipitation
in the presence of hard water, that is, in the presence of large amounts of calcium
and magnesium ions in the water utilized to prepare the hydraulic fluid of the invention.
In addition, the alkyldialkanolamides contribute to the antiwear and extreme pressure
performance of the composition as well as to the metal corrosion resistance which
is desirable in such fluidsn The alkyldialkanolamides in aqueous solution are completely
stable under neutral and alkaline conditions and show little tendency to hydrolyze
or decompose on storage.
[0036] The hydraulic fluids of the invention may consist of about 25 percent to about 99
percent water and about 75 percent to about 1 percent concentrate. These concentrates
may comprise water, the viscosity increasing compound and thickener possibly in combination
with a lower alcohol, the water-soluble esters of ethoxylated aliphatic acid and/or
ethoxylated alcohol ethers and/or sulfur containing compound; and/or phosphate ester,
and/or alkyldialkanolamide and, in addition, can contain defoamers, corrosion inhibitors
and metal deactivators or chelating agents. Preferably, the final fluids consist of
about 50 percent to 99 percent water and about 50 percent to about 1 percent concentrate.
The fluids are easily formulated at room temperature. Generally, distilled or de-ionized
water is used for water-glycol fluids and tap water is used for high water fluids.
[0037] The amount of sulfur-containing compound in'the hydraulic fluid concentrate of the
invention (when a concentrate is used) is generally about 0 to 10 percent by weight.
The concentration of the phosphate ester in the hydraulic fluid concentrate of the
invention is generally about 0 to 7.0 percent by weight of the concentrate. The concentration
of the water-soluble ester of the ethoxylated alipahtic acid and/or ethoxylated alcohol
ether in the ; hydraulic fluid concentrate of the invention is generally about 0 percent
to about 7.0 percent by weight. The minimum amount of any of the above components
when incorporated in the concentrate is 1.0 percent. Preferably, the proportion by
weight of each of these three components is 1.0 to 5.0 percent in a high water fluid
concentrate. They generally are not present in a water-glycol fluid.
[0038] The percent by weight alkanolamide in the concentrate is about 1 to 7, preferably
about 1 to 5 based upon the total weight of the concentrate.
[0039] The metal deactivators and corrosion inhibitors which can be added either to the
concentrate or to the hydraulic fluid or metalworking compositions of the invention
are as follows:
Liquid-vapor corrosion inhibitors may be employed and can be any of the alkali metal
nitrites, nitrates and benzoates. certain amines are also useful. The inhibitors can
be used individually or in combinations. Representative examples of the preferred
alkali metal nitrates and benzoates which are useful are as follows: sodium nitrate,
potassium nitrate, calcium nitrate, barium nitrate, lithium nitrate, strontium nitrate,
sodium benzoate, potassium benzoate, calcium benzoate, barium benzoate, .lithium benzoate
and strontium benzoate.
[0040] Representative amine-type corrosion inhibitors are ; as follows: butylamine, propylamine,
n-octylamine, hexyl- amine, morpholine, N-ethyl morpholine, N-methyl morpholine, aniline,
triphenylamine, aminotoluene, ethylene diamine, dimethylaminopropylamine, N,N-dimethyl
ethanolamine, triethanolamine, diethanolamine, monoethanolamine, 2-methyl pyridine,
4-methyl pyridine, piperazine, dimethyl morpholine, α- and γ-picoline, isopropylaminoethanol
and 2-amino-2-methylpropanol. These amines also function to neutralize the free acid
form of the phosphate ester converting ie to the salt form.
[0041] Imidazolines can be used for their known corrosion inhibiting properties with respect
to cast iron and steel. Useful imidazolines are heterocyclic nitrogen compounds having
the formula:

wherein R
4 is hydrogen or a monovalent radical selected from the group consisting of alkyl of
1 to 18 carbon atoms, alkylene of 1 to 18 carbon atoms, aryl, and alkylaryl having
1 to 18 carbon atoms in the alkyl portion, wherein
R3 is a divalent radical selected from the group consisting of alkyl and alkoxy having
2 to 18 carbon atoms where the alkoxy is derived from alkylene oxides selected from
the group consisting of ethylene oxide, propylene'oxide, butylene oxide, tetrahydrofuran
and mixtures thereof and wherein M is an alkali metal.
[0042] It is also contemplated to add other known corrosion inhibitors. Besides the amines,
alkali metal nitrates, benzoates and nitrites listed above, the alkoxylated fatty
acids are useful as. corrosion inhibitors.
[0043] The above corrosion inhibitors are employed in the hydraulic tluid concentrates in
total amount of about 2 to 25 percent by weight, preferably about 5 to 15 percent
by weight. More specifically, it is preferred to employ one or more of the following
as corrosion inhibitor: benzoates or benzoic acid in amount of about 1 to 5 percent,
amines in amount of about 2 to 10 percent, and imidazolines in amount of about 2 to
10 percent all by weight of the total amount of concentrate.
[0044] Metal deactivators may be used primarily to chelate copper and copper alloys. Such
materials are well known in the art and individual compounds can be selected from
the broad classes of materials useful for this purpose such as the various triazoles
and thiazoles as well as the amine derivatives of salicylidenes. Representative specific
examples of these metal deactivators are as follows: benzotriazole, tolyltriazole,
2-mercaptobenzothiazole, sodium 2-mercaptobenzothiazole, and N,N'-disalicylidene-1,2-propanediamine.
The concentration of metal deactivator to water in the hydraulic fluid concentrates
of the invention is generally about 2 to 10 percent by weight and preferably about
3 to 5 percent by weight.
[0045] Conventional defoamers such as the well known organic surfactant defoamers, for example
nonionic defoamers such as the polyoxyalkylene type nonionic surfactants, may also
be employed in normal amounts. Preferred amounts are about 0.5 to 5.0 percent by weight
of the total amount of concentrate.
[0046] Lower alcohols, i.e., those with about 2 to 10 carbon atoms, for example, methanol,ethanol,
propanol, ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol
and glycerol, may also be employed in normal amounts. Ethylene glycol and propylene
glycol are preferred. Preferred amounts of lower alcohols when employed are about
5 to 80 percent by weight of the concentrate. Where large amounts of lower alcohols
are used, such as in so-called water-glycol fluids, the fluid is not normally sold
as a concentrate but is sold as a ready-to-use fluid. The concentroate may contain
other conventional hydraulic fluid additives and possibly some impurities in normal
minimal amounts.
[0047] The phosphate esters and esters of ethoxylated aliphatic acids and alcohols are water-soluble
in the sense that no special method is required to disperse these materials in water
and keep them in suspension over long periods of time. As a means of reducing corrosion,
the pH of the water in the fluids of the invention is maintained above 7.0, preferably
7.0 to about 11.0, and most preferably. 9 to about 10.5. Preferably, pH of the fluid
concentrates is adjusted with an alkali metal or alkaline earth metal hydroxide, or
carbonate, ammonia or an amine. Where these are employed, benzoic acid may be employed
in lieu of alkali metal benzoates. The sulfurized molybdenum or antimony compounds
on the other hand are insoluble in water and require emulsification prior to use,
for instance, with anionic or nonionic surfactants. Useful representative anionic
or nonionic surfactants are: sodium petroleum sulfonate, i.e., sodium dodecylbenzene
sulfonate; polyoxyethylated fatty alcohol or fatty acid and polyoxyethylated alkyl
phenol.
[0048] The concentrates of the hydraulic fluids of this invention can be made up completely
free of water or contain any desired amount of water but preferably contain up to
85 percent by weight of water to increase fluidity and provide ease of blending at
the point of use. As pointed out above, these concentrates are typically diluted with
water in the proportion of 1:99 to 75:25 to make up the final hydraulic. fluid.
[0049] The preferred final hydraulic fluid of the invention may include 25 to 99 percent
by weight water and by weight one or more of the following conventional additives:
about 0.01 to 3.0 percent water soluble ester of exothylated aliphatic acid and/or
ethoxylated alcohol ether, about 0.01 to 2.0 percent sulfur-containing compound, abdut
0.01 to 3.0 percent ethoxylated phosphate ester, or salt thereof, about 0.01 to 3
percent alkanolamide, about 0.05 to 10 percent corrosion inhibitors, and most preferably
one or more of the following three corrosion inhibitors in amount of about 0.01 to
2 percent benzoic acid.and/or benzoates, about 0.02 to 3 percent amine type corrosion
inhibitors and about 0.02 to 2 percent ethoxylated imidazoline; about 0.02 to 5 percent
metal deactivators, about 0.01 to 2.0 percent defoamers and about 1 to 50 percent
lower alcohol, plus other conventional additives such as dyes and impurities in normal
amounts.
[0050] The following examples more fully describe the hydraulic fluids of the invention
and show the unexpected results obtained by their use.
[0051] Thickener #1 is a branched heteric copolymer of ethylene oxide, and 1,2-propylene
oxide having a molecular weight of i6,000 using trimethylolpropane as an initiator
and containing 85 percent oxyethylene units, and 15 percent oxypropylene units. This
basic heteric copolymer is further reacted with a mixture of alpha olefin epoxides
having 15 to 18 carbon atoms.
[0052] Thickener #2 is a branched heteric copolymer of ethylene oxide and 1,2-propylene
oxide using trimethylol propane as an initiator and containing 85 percent oxyethylene
units, and 15 percent oxypropylene units. This basic heteric copolymer is further
reacted with a mixture o6 alpha-olefin epoxides having 15 to 18 carbon atoms. The
total molecular weight is approximately 17,000.
[0053] Thickener #3 is a branched heteric copolymer of ethylene oxide and 1,2-propylene
oxide using trimethylol propane as an initiator and containing approximately 85 percent
oxyethylene units, and approximately 15 percent oxypropylene units. This basic heteric
copolymer is further reacted with a mixture of alpha olefin epoxides having 15 to
18 carbon atoms. The molecular weight is approximately 15,000.
[0054] The examples are intended for the purpose of illustration. Throughout the application,
all parts, proportions, and percentages are by weight and all temperatures are in
degrees centigrade unless otherwise noted.
Examples 1 and 2
[0055] A hydraulic fluid inhibitor concentrate was prepared by blending 30 parts by weight
morpholine and 8 parts by weight of a 50 percent by weight aqueous solution of sodium
mercaptobenzothiazole.
[0056] From the concentrate two stock solutions of the composition of Table I below were
prepared:

[0057] As can be seen from Table I, the addition of just 1 percent lauric acid increased
the viscosity of the hydraulic fluid almost ten times.
Examoles 3-8
[0058] Eight hydraulic fluids were prepared by first blending the following components in
the amounts set forth in Table II below:

[0059] From the base fluid of Table II above, the hydraulic fluids of Examples 3 to 8 were
prepared by blending the components in the amount set forth in Table III below. The
viscosities of the fluids were determined at ; 100°F and are set forth in Table III
below:

Examples 9-16
[0060] Eight hydraulic fluids were prepared by blending the following components in the
amounts set forth in Table IV below. The viscosities of the fluids were determined
at 100°F and are set forth in Table IV below:

[0061] These examples demonstrate that 1) in a water-glycol formulation, the greatest effect
is seen with acid and without,amines; 2) in a high-water fluid, the greatest effect
is seen in the presence of both amines and acid.
Examples 17-22
[0062] Eight hydraulic fluids were prepared by first blending the following components in
the amounts set forth in Table V below:

[0063] From the base fluid of Table V above, the hydraulic fluids of Examples 17 to 22 were
prepared by blending the components in the amounts set forth in Table VI below. The
viscosities of the fluids were determined and are set forth in Table VI below:

Examples 23-26
[0064] Four hydraulic fluids were prepared by first blending 800 parts by weight of base
fluid from Table V above with 4 parts by weight additional thickener #2, creating
a new base fluid that is 0.5 percent richer in thickener concentration. From this
base fluid, the. hydraulic fluids of Examples 23 to 26 were prepared by blending the
components in the amounts set forth in Table VII below. The viscosities of the fluids
were determined and are set forth in Table VII below:

[0065] These examples show that: 1) small increases in the concentration of the thickener
produce a large increase in viscosity in the presence of the organic acid (compare
Examples 23-26 to Examples 17-19 and 22); 2) the straight chain acids show the effect
more strongly but branched acids also show this effect.