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Claims  |
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What is claimed is:
1. Azeotrope--like compositions consisting essentially of from about 89 to
about 99.5 weight percent of 1,1,2,3,3,-pentafluoropropane and from about
0.5 to about 11 weight percent of methanol and from about 0 to about 1
weight percent nitromethane wherein said compositions boil at about
38.1.degree. C. at 760 mm Hg.
2. The azeotrope-like compositions of claim 1 consisting essentially of
from about 90 to about 98.2 weight percent said
1,1,2,3,3-pentafluoropropane and from about 1.8 to about 10 weight percent
said methanol and from about 0 to about 0.5 weight percent said
nitromethane wherein said compositions boil at about 38.1.degree. C. at
760 mm Hg.
3. The azeotrope-like compositions of claim 1 consisting essentially of
from about 90.6 to about 97.6 weight percent said
1,1,2,3,3-pentafluoropropane and from about 2.4 to about 9.4 weight
percent said methanol and from about 0 to about 0.4 weight percent said
nitromethane wherein said compositions boil at about 38.1.degree. C. at
760 mm Hg.
4. Azeotrope-like compositions consisting essentially of from about 97 to
about 99.99 weight percent of 1,1,2,3,3-pentafluoropropane and from about
0.01 to about 3 weight percent of ethanol and from about 0 to about 1
weight percent nitromethane wherein said compositions boil at about
8.5.degree. C. at 760 mm Hg.
5. The azeotrope-like compositions of claim 4 consisting essentially of
from about 98.5 to about 9.99 weight percent said
1,1,2,3,3-pentafluoropropane and from about 0.01 to about 1.5 weight
percent said ethanol and from about 0 to about 0.5 weight percent said
nitromethane wherein said compositions boil at about 38.5.degree. C. at
760 mm Hg.
6. The azeotrope-like compositions of claim 4 consisting essentially of
from about 98.8 to about 99.99 weight percent said
1,1,2,3,3-pentafluoropropane and from about 0.01 to about 1.2 weight
percent said ethanol and from about 0 to about 0.4 weight percent said
nitromethane wherein said compositions boil at about 38.5.degree. C. at
760 mm Hg.
7. The azeotrope-like compositions of claim 1 wherein an effective amount
of an inhibitor is present in said compositions to accomplish at least one
of the following: inhibit decomposition of the compositions, react with
undesirable decomposition products of the compositions, and prevent
corrosion of metal surfaces.
8. The azeotrope-like composition of claim 7 wherein said inhibitor is
selected from the group consisting of alkanols having 4 to 7 carbon atoms,
nitroalkanes having 2 to 3 carbon atoms, phosphite esters having 12 to 30
carbon atoms, ethers having 3 or 4 carbon atoms, acetals having 4 to 7
carbon atoms, ketones having 3 to 5 carbon atoms, and amines having 6 to 8
carbon atoms.
9. The azeotrope-like compositions of claim 7 wherein said inhibitor is
selected from the group consisting of 1,2-expoyalkanes having 2 to 7
carbon atoms.
10. The azeotrope-like compositions of claim 4 wherein an effective amount
of an inhibitor is present in said compositions to accomplish at least one
of the following: inhibit decomposition of the compositions, react with
undesirable decomposition products of the compositions, and prevent
corrosion of metal surfaces.
11. The azeotrope-like composition of claim 10 wherein said inhibitor is
selected from the group consisting of alkanols having 4 to 7 carbon atoms,
nitroalkanes having 2 to 3 carbon atoms, phosphite esters having 12 to 30
carbon atoms, ethers having 3 to 4 carbon atoms, acetals having 4 to 7
carbon atoms, ketones having 3 to 5 carbon atoms, and amines having 6 to 8
carbon atoms.
12. The azeotrope-like compositions of claim 10 wherein said inhibitor is
selected from the group comsisting of 1,2-epoxyalkanes having 2 to 7
carbon atoms.
13. A method of dissolving contaminants or removing contaminants from the
surface of a substrate which comprise the step of:
treating said surface of substrate with said azeotrope-like composition of
claim 1 as solvent.
14. A method of dissolving contaminants or removing contaminants from the
surface of a substrate which comprises the step of:
treating said surface of said substrate with said azeotrope-like
composition of claim 2 as solvent.
15. A method of dissolving contaminants or removing contaminants from the
surface of a substrate which comprises the step of:
treating said surface of said substrate with said azeotrope-like
composition of claim 3 as solvent.
16. A method of dissovling contaminants or removing contaminants form the
surface of a substrate which comprises the step of:
treating said surface of said substrate with said azeotrope-like
composition of claim 4 as solvent.
17. A method of dissolving contaminants or removing contaminants from the
surface of a substrate which comprises the step of:
treating said surface of said substrate with said azeotrope-like
composition of claim 5 as solvent.
18. A method of dissolving contaminants or removing contaminants from the
surface of a substrate which comprises the step of:
treating said surface of said substrate with said azeotrope-like
composition of claim 6 as solvent. |
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Claims  |
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Description  |
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BACKGROUND OF THE INVENTION
Vapor degreasing and solvent cleaning with fluorocarbon based solvents have
found widespread use in industry for the degreasing and otherwise cleaning
of solid surfaces, especially intricate parts and difficult to remove
soils.
In its simplest form, vapor degreasing or solvent cleaning consists of
exposing a room temperature object to be cleaned to the vapors of a
boiling solvent. Vapors condensing on the object provide clean distilled
solvent to wash away grease or other contamination. Final evaporation of
solvent from the object leaves behind no residue as would be the case
where the object is simply washed in liquid solvent.
For difficult to remove soils where elevated temperature is necessary to
improve the cleaning action of the solvent, or for large volume assembly
line operations where the cleaning of metal parts and assemblies must be
done efficiently and quickly, the conventional operation of a vapor
degreaser consists of immersing the part to be cleaned in a sump of
boiling solvent which removes the bulk of the soil, thereafter immersing
the part in a sump containing freshly distilled solvent near room
temperature, and finally exposing the part to solvent vapors over the
boiling sump which condense on the cleaned part. In addition, the part can
also be sprayed with distilled solvent before final rinsing.
Cold cleaning is another application where a number of solvents are used.
In most cold cleaning applications, the soiled part is either immersed in
the fluid or wiped with rags or similar objects soaked in solvents and
allowed to air dry.
Fluorocarbon solvents, such as trichlorotrifluoroethane, have attained
widespread use in recent years as effective, nontoxic, and nonflammable
agents useful in degreasing applications and other solvent cleaning
applications. Trichlorotrifluoroethane has been found to have satisfactory
solvent power for greases, oils, waxes and the like. It has therefore
found widespread use for cleaning electric motors, compressors, heavy
metal parts, delicate precision metal parts, printed circuit boards,
gyroscopes, guidance systems, aerospace and missile hardware, aluminum
parts and the like.
Azeotropic or azeotrope-like compositions are desired because they do not
fractionate upon boiling. This behavior is desirable because in the
previously described vapor degreasing equipment with which these solvents
are employed, redistilled material is generated for final rinse.cleaning.
Thus, the vapor degreasing system acts as a still. Unless the solvent
composition exhibits a constant boiling point, i.e., is azeotrope-like,
fractionation will occur and undesirable solvent distribution may act to
upset the cleaning and safety of processing. Preferential evaporation of
the more volatile components of the solvent mixtures, which would be the
case if they were not azeotrope-like, would result in mixtures with
changed compositions which may have less desirable properties, such as
lower solvency towards soils, less inertness towards metal, plastic or
elastomer components, and increased flammability and toxicity. The art has
looked towards azeotrope or azeotrope-like compositions including the
desired fluorocarbon components such as trichlorotrifluoroethane which
include components which contribute additionally desired characteristics,
such as polar functionality, increased solvency power, and stabilizers.
The art is continually seeking new fluorocarbon, hydrofluorocarbon, and
hydrochlorofluorocarbon based azeotrope-like mixtures which offer
alternatives for new and special applications for vapor degreasing and
other cleaning applications. Currently, of particular interest, are
fluorocarbon, hydrofluorocarbon, and hydrochlorofluorocarbon based
azeotrope-like mixtures with minimal or no chlorine which are considered
to be stratospherically safe substitutes for presently used
chlorofluorocarbons (CFCs). The latter are suspected of causing
environmental problems in connection with the earth's protective ozone
layer. Mathematical models have substantiated that hydrofluorocarbons,
such as 1,1,2,3,3.pentafluoropropane (known in the art as HFC-245ea), will
not adversely affect atmospheric chemistry, being negligible contributors
to ozone depletion and to green house global warming in comparison to
chlorofluorocarbons such as 1,1,2-trichloro-1,2,2-trifluoroethane
(CFC-113).
European Publication 431,458 published Jun. 12, 1991 teaches a mixture of
1,1,2,3,4,4-hexafluorobutane and ethanol. U.S. Pat. No. 5,023,010 teaches
an azeotropic mixture of 1,1,1,2,3,3-hexafluoro-3-methoxypropane and
methanol. U.S. Pat. No. 5,035,830 teaches an azeotropic mixture of
hexafluoropropylene/ethylene cyclic dimer and methanol or ethanol. U.S.
Pat. No. 5,064,559 teaches an azeotropic mixture of
1,1,1,2,3,4,4,5,5,5-decafluoropentane and methanol or ethanol. U.S. Pat.
No. 5,073,291 teaches an azeotrope-type mixture of
1,4-dihydroperfluorobutane and methanol.
U.S. Pat. Nos. 5,073,288 and 5,073,290 teach binary azeotrope-like
compositions of 1,1,1,2,2,3,5,5,5-nonafluoro-4-trifluoromethylpentane or
1,1,1,2,2,5,5,5-octafluoro-4-trifluoromethylpentane and methanol or
ethanol.
DETAILED DESCRIPTION OF THE INVENTION
Our solution to the need in the art for substitutes for chlorofluorocarbon
solvents is mixtures comprising 1,1,2,3,3-pentafluoropropane and methanol
or ethanol and optionally nitromethane. Also, novel azeotrope-like or
constant.boiling compositions have been discovered comprising
1,1,2,3,3-pentafluoropropane and methanol or ethanol and optionally
nitromethane.
Preferably, the novel azeotrope-like compositions comprise effective
amounts of 1,1,2,3,3-pentafluoropropane and methanol or ethanol and
optionally nitromethane. The term "effective amounts" as used herein means
the amount of each component which upon combination with the other
component, results in the formation of the present azeotrope-like
compositions.
The azeotrope-like compositions comprise from about 89 to about 99.99
weight percent of 1,1,2,3,3-pentafluoropropane and from about 0.01 to
about 11 of methanol or ethanol and from 0 to about 1 weight percent
nitromethane.
The present azeotrope-like compositions are advantageous for the following
reasons. The 1,1,2,3,3-pentafluoropropane is a negligible contributor to
ozone depletion and has a boiling point of 40.degree. C. The methanol and
ethanol components have good solvent properties. Thus, when these
components are combined in effective amounts, an efficient azeotrope-like
solvent results.
The preferred azeotrope-like compositions are in the Table below where
1,1,2,3,3-pentafluoropropane is abbreviated as HFC-245ea. In the Table,
the numerical ranges are understood to be prefaced by "about".
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MORE MOST BOIL-
PRE- PRE- PRE- ING
FERRED FERRED FERRED POINT
COM- RANGE RANGE RANGE (.degree.C.)
PONENTS (WT. %) (WT. %) (WT. %) (760 mmHg)
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HFC-245ea
89-99.5 90-98.2 90.6-97.6
38.1 .+-. 0.4
Methanol
0.5-11 1.8-10 2.4-9.2
Nitro- 0-1 0-0.5 0-0.4
methane
HFC-245ea
97-99.99
98.5-99.99
98.8-99.99
38.5 .+-. 0.2
Ethanol 0.01-3 0.01-1.5 0.01-1.2
Nitro- 0-1 0-0.5 0-0.4
methane
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All compositions within the indicated ranges, as well as certain
compositions outside the indicated ranges, are azeotrope-like, as defined
more particularly below.
The precise azeotrope compositions have not been determined but have been
ascertained to be within the above ranges. Regardless of where the true
azeotropes lie, all compositions with the indicated ranges, as well as
certain compositions outside the indicated ranges, are azeotrope like, as
defined more particularly below.
The term "azeotrope-like composition" as used herein is intended to mean
that the composition behaves like an azeotrope, i.e. has constant-boiling
characteristics or a tendency not to fractionate upon boiling or
evaporation. Thus, in such compositions, the composition of the vapor
formed during boiling or evaporation is identical or substantially
identical to the original liquid composition. Hence, during boiling or
evaporation, the liquid composition, if it changes at all, changes only to
a minimal or negligible extent. This is to be contrasted with
non-azeotrope-like compositions in which during boiling or evaporation,
the liquid composition changes to a substantial degree. As is readily
understood by persons skilled in the art, the boiling point of the
azeotrope-like composition will vary with the pressure.
The azeotrope-like compositions of the invention are useful as solvents in
a variety of vapor degreasing, cold cleaning and solvent cleaning
applications including defluxing and dry cleaning.
In the process embodiment of the invention, the azeotrope-like compositions
of the invention may be used to clean solid surfaces by treating said
surfaces with said compositions in any manner well known to the art such
as by dipping or spraying or use of conventional degreasing apparatus. In
one process embodiment of the invention, the azeotrope-like compositions
of the invention may be used to dissolve contaminants or remove
contaminants from the surface of a substrate by treating the surfaces with
the compositions in any manner well known to the art such as by dipping or
spraying or use of conventional degreasing apparatus wherein the
contaminants are substantially removed or dissolved.
The 1,1,2,3,3-pentafluoropropane of the present invention may be prepared
by any known method such as the reaction of commercially available
tetrahydrofuran and cobalt trifluoride as taught by J. Burdon et al.,
"Partial Fluorination of Tetrahydrofuran with Cobalt Trifluoride", J. of
Chem. Soc. (C), 1739 (1969). The methanol: ethanol: and nitromethane
components of the novel solvent azeotrope-like compositions of the
invention are known materials and are commercially available.
EXAMPLE 1
This example shows that a minimum in the boiling point versus composition
curve occurs in the region of 95 weight percent
1,1,2,3,3-pentafluoropropane (hereinafter HFC-245ea) and 5 weight percent
methanol indicating that an azeotrope forms in the neighborhood of this
composition.
A microebulliometer which consisted of a 15 milliliter round bottom double
neck flask containing a magnetic stirbar and heated with an electrical
heating mantel was used. Approximately 2.5 milliliters of the lower
boiling material, HFC-245ea, was charged into the microebulliometer and
methanol was added in small measured increments by an automated syringe
capable of injecting microliters. The temperature was measured using a
platinum resistance thermometer and barometric pressure was measured. An
approximate correction to the boiling point was done to obtain the boiling
point at 760 mm Hg.
The boiling point was measured and corrected to 760 mm Hg (101 kPa) for
various mixtures of HFC-245ea and methanol. Interpolation of the data
shows that a minimum boiling point occurs in the region of about 2.4 to
about 9 weight percent methanol. The best estimate of the position of the
minimum is 4.7 weight percent methanol, although the mixtures are
constant-boiling, to within 0.4.degree. C., in the region of 0.5 to 10
weight percent methanol. A minimum boiling azeotrope is thus shown to
exist in this composition range.
No attempt was made to fully characterize and define the outer limits of
the composition ranges which are constant boiling. Anyone skilled in the
art can readily ascertain other constant boiling or essentially constant
boiling mixtures containing the same components.
EXAMPLE 2
Example 1 was repeated except that ethanol was used instead of methanol.
Approximately 2.8 milliliters of the lower boiling material, HFC-245ea,
were initially charged into the microebulliometer and ethanol was added in
small measured increments by an automated syringe capable of injecting
microliters. The boiling point was measured and corrected to 760 mm Hg
(101 kPa), for various mixtures of HFC-245ea and ethanol. Interpolation of
these data shows that a minimum boiling point occurs in the region of
about 0.1 to about 0.8 weight percent ethanol. The best estimate of the
position of the minimum is 0.5 weight percent ethanol, although the
mixtures are constant.boiling, to within 0.2.degree. C., in the region of
0.01 to 2 weight percent ethanol. A minimum boiling azeotrope is thus
shown to exist in this composition range.
EXAMPLES 3 AND 4
Performance studies are conducted wherein metal coupons are cleaned using
the present azeotrope-like compositions as solvents. The metal coupons are
soiled with various types of oils and heated to 93.degree. C. so as to
partially simulate the temperature attained while machining and grinding
in the presence of these oils.
The metal coupons thus treated are degreased in a three-sump vapor phase
degreaser machine. In this typical three-sump degreaser, condenser coils
around the lip of the machine are used to condense the solvent vapor which
is then collected in a sump. The condensate overflows into cascading sumps
and eventually goes into the boiling sump.
The metal coupons are held in the solvent vapor and then vapor rinsed for a
period of 15 seconds to 2 minutes depending upon the oils selected. The
azeotrope-like compositions of Examples 1 and 2 are used as the solvents.
Cleanliness testing of the coupons is done by measurement of the weight
change of the coupons using an analytical balance to determine the total
residual materials left after cleaning.
EXAMPLES 5 AND 6
Each solvent of Examples 1 and 2 above is added to mineral oil in a weight
ratio of 50:50 at 27.degree. C. Each solvent is miscible in the mineral
oil.
EXAMPLES 7 AND 8
Metal coupons are soiled with various types of oil. The soiled metal
coupons are immersed in the solvents of Examples 1 and 2 above for a
period of 15 seconds to 2 minutes, removed, and allowed to air dry. Upon
visual inspection, the soil appears to be substantially removed.
EXAMPLES 9 AND 10
Metal coupons are soiled with various types of oil. The soiled metal
coupons are sprayed with the solvents of Examples 1 and 2 above and
allowed to air dry. Upon visual inspection, the soil appears to be
substantially removed.
Known additives may be used with the present azeotrope-like compositions in
order to tailor the composition for a particular use. Inhibitors may be
added to the present azeotrope-like compositions to inhibit decomposition
of the compositions; react with undesirable decomposition products of the
compositions; and/or prevent corrosion of metal surfaces. Any or all of
the following classes of inhibitors may be employed in the invention:
alkanols having 4 to 7 carbon atoms, nitroalkanes having 2 to 3 carbon
atoms, 1,2-epoxyalkanes having 2 to 7 carbon atoms, phosphite esters
having 12 to 30 carbon atoms, ethers having 3 or 4 carbon atoms,
unsaturated compounds having 4 to 6 carbon atoms, acetals having 4 to 7
carbon atoms, ketones having 3 to 5 carbon atoms, and amines having 6 to 8
carbon atoms. Other suitable inhibitors will readily occur to those
skilled in the art. In spraying applications, the azeotrope-like
compositions may be sprayed onto a surface by using a propellant.
The inhibitors may be used alone or in mixtures thereof in any proportions.
Typically, up to about 2 percent based on the total weight of the
azeotrope-like composition of inhibitor might be used.
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Description  |
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