US2999817A - Azeotropic composition - Google Patents

Azeotropic composition Download PDF

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Publication number
US2999817A
US2999817A US49436A US4943660A US2999817A US 2999817 A US2999817 A US 2999817A US 49436 A US49436 A US 49436A US 4943660 A US4943660 A US 4943660A US 2999817 A US2999817 A US 2999817A
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United States
Prior art keywords
solvent
azeotropic composition
azeotropic
methylene chloride
trifluoroethane
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US49436A
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Frank A Bower
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EIDP Inc
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EI Du Pont de Nemours and Co
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Priority to US49427A priority patent/US2999816A/en
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41NPRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
    • B41N3/00Preparing for use and conserving printing surfaces
    • B41N3/006Cleaning, washing, rinsing or reclaiming of printing formes other than intaglio formes
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/50Solvents
    • C11D7/5036Azeotropic mixtures containing halogenated solvents
    • C11D7/504Azeotropic mixtures containing halogenated solvents all solvents being halogenated hydrocarbons
    • C11D7/5059Mixtures containing (hydro)chlorocarbons
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G5/00Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
    • C23G5/02Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
    • C23G5/028Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing halogenated hydrocarbons
    • C23G5/02809Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing halogenated hydrocarbons containing chlorine and fluorine
    • C23G5/02812Perhalogenated hydrocarbons
    • C23G5/02816Ethanes
    • C23G5/02819C2Cl3F3

Definitions

  • This invention relates to an azeotropic composition and particularly to the azeotropic mixture of 1,1,2-triohloro- 1,2,2-trifluoroethane and methylene chloride.
  • chlorofluorome'thanes and chlorofluoroethanes have attained widespread'use as specialty solvents in recent years, particularly trichlorofluoromethane and trichlorotrifluoroethane. Both of these' compounds are relatively low boiling liquids (CCl F, 23.8 C.; CCI FCCIF 47.6" C.), which are nontoxic and nonfiamrnable, and which have good solvent power for greases, oils, waxes and the like. They have therefore found widespread use for cleaning electricmotors, compressors, oxygen storage tanks, photographic film, lithographic plates, typewriters; instruments gauges, sound tape, and as noncorrosivebrines.
  • the chlorofluoromethanes and chlorofluoroethanes have insufficient solvent power alone. This is particularly true in the electronic industry during the manufacture of printed circui L.
  • Printed circuits are well known in the electronics art; and consist of a circuit formed from a soft metal on a solid, nonconducting surface such as a reinforced phenolic 1 resin. During manufacture, the solid surface is coated with the metal, the desired portion of metal is coated with an impervious coating, and the excess metal is removed by etching with a suitable acid. After the excess metal has been removed, it is necessary to remove the impervious coating because solder joints must be made to the printed circuit" and these will not form if the coating is present.
  • the circuits are coated with a rosin flux to permit the joints to be soldered, which rosin flux must then be removed.
  • the chlorofluoromethane and chlorofluoroethane solvents do not have sufiicient solvent power to clean printed circuits; that is, to etfectively remove the rosin flux.
  • this invention comprises an azeotropic composition consisting of about 52% by weight of 1,1,2- trichloro-l,2,2atrifluoroethane and about 48% by weight of methylene chloride and boiling at 37 C. at 760 mm. pressure.
  • the azeotropic mixture of this invention has the desired properties which render it useful for this pur'p'oseI r i
  • the azeotropic mixture of l,l,2-trichloro-l,2,2-trifluoroethane and methylene chloride is of special value for cleaning printed circuits.
  • the l, --l,2-trichloro-l,2,2- trifiuoroethane alone is'not an elfective' solvent for cleaning printed circuits, and has no deleteriousfefiect on the boards which form the bases of the printed circuits.
  • Methylene chloride alone deleteriously ,aifects such boards, particularly laminated boards impregnated with phenolic resins, causing softening, swelling "and delamination of such boards and dissolving certain marking inks which are used to code various electronic components in the printed circuit assembly.
  • the azeotropic mixture of this invention does not have these effects and is an excellent solvent for such purpose.
  • the azeotrope of this invention has several advantages over the solvents heretofore employed for cleaning printed circuits.
  • Trichloroethylene, tetrachloroethylene, and methyl chloroform are unstable and require stabilizers, whereas the azeotropic composition of this invention does not require a stabilizer, has a more favorable evaporation rate (is lower boiling), and is considerably less toxic than such solvents.
  • the azeotropic composition of this invention is more effective as a solvent for such purposes than trichloroethylene and tetrachloroethylene.
  • Inhibited methyl chloroform (containing dioxane as a stabilizer) is too strong a solvent and attacks the backing of the printed circuits.
  • the azeotropic composition of this invention was established by the fractional distillation of a mixture containing 20% by weight'of l,l,2-trichloro-1,2,2-trifluoroethane and by weight of methylene chloride.
  • Printed circuit boards are usually prepared by impregnating glass cloth, nylon, or paper laminates with a phenol-formaldehyde resin or an epoxy resin.
  • Printed circuits are prepared by a variety of methods. In a typical procedure, the board consists originally of a phenolic resin impregnated base to which is bonded a sheet of copper, 2 to 4 mils thick, covering one surface of the board. The desired circuitis drawn on the copper with an asphalt based ink, using the silk screen method.
  • excess copper is then removed by etching with a ferric chloride-hydrochloric acid bath, sometimes containing ammonium chloride, leaving on the board the copper that is covered by the ink.
  • the asphalt ink is removed by cleaning with the azeotropic composition of this invention in an ultrasonic bath (some mechanical scrubbing is often used).
  • the entire surface of the board is then coated with a rosin flux and dried.
  • the electronic components (resistors, capacitors, etc.) are then added at the proper places for soldering to the circuit.
  • the board is then passed over a molten solder bath, contacting the desired joints With the molten metal, whereby the soldering is effected.
  • the excess rosin flux remaining on the board must be removed since, if present in the final assembly, it will lead to corrosion, poor electrical resistance and other deleterious properties.
  • the board is cleaned by placing it in an ultrasonic bath operating at about 32 kilocycles per second and at about 25 C., where it remains for one minute. If 1,1,2-trichloro-1,2,2-trifluoroethane is used alone as the solvent in the bath, it has no effect on the rosin flux. If trichloroethylene is used as the solvent in the bath, about 5% to about 50% of the flux remains after the treatment. If the same cleaning operation is repeated on another circuit board using the azeotropic mixture of 1,1,2-trichloro- 1,2,2-trifluoroethane and methylene chloride as the solvent, the rosin fiux is completely removed. Neither the 1,1,2 trichloro-1,2,2-trifluoroethane nor the azeotropic mixture has any efiect on the board which constitutes the backing of the printed circuit.
  • azeotropic composition of this invention in cleaning printed circuits is given for illustrative purposes solely, that this invention is not restricted to such specific embodiment, and that other techniques may be employed. Also, the azeotropic composition can be used for other purposes as indicated in the general description.
  • A11 azetropic composition consisting of about 52% by Weight of 1,1,2-trich1oro-1,2,2-trifluoroethane and about 48% by weight of methylene chloride and boiling at 37 C. and 760 mm. pressure.

Description

United States Patent C "ice j 2,999,817 AZEOTROPIC COMPOSITION corporation of Delaware No Drawing. Filed Aug. 15, 1960, Ser. No. 49,436
1 Claim. '(Cl. 252172) This invention relates to an azeotropic composition and particularly to the azeotropic mixture of 1,1,2-triohloro- 1,2,2-trifluoroethane and methylene chloride.
Several of the chlorofluorome'thanes and chlorofluoroethanes have attained widespread'use as specialty solvents in recent years, particularly trichlorofluoromethane and trichlorotrifluoroethane. Both of these' compounds are relatively low boiling liquids (CCl F, 23.8 C.; CCI FCCIF 47.6" C.), which are nontoxic and nonfiamrnable, and which have good solvent power for greases, oils, waxes and the like. They have therefore found widespread use for cleaning electricmotors, compressors, oxygen storage tanks, photographic film, lithographic plates, typewriters; instruments gauges, sound tape, and as noncorrosivebrines.
For certain solvent purposes however, the chlorofluoromethanes and chlorofluoroethanes have insufficient solvent power alone. This is particularly true in the electronic industry during the manufacture of printed circui L. Printed circuits are well known in the electronics art; and consist of a circuit formed from a soft metal on a solid, nonconducting surface such as a reinforced phenolic 1 resin. During manufacture, the solid surface is coated with the metal, the desired portion of metal is coated with an impervious coating, and the excess metal is removed by etching with a suitable acid. After the excess metal has been removed, it is necessary to remove the impervious coating because solder joints must be made to the printed circuit" and these will not form if the coating is present. After the imprevious coating is removed, the circuits are coated with a rosin flux to permit the joints to be soldered, which rosin flux must then be removed. The chlorofluoromethane and chlorofluoroethane solvents do not have sufiicient solvent power to clean printed circuits; that is, to etfectively remove the rosin flux.
It is an object of this invention to provide a novel azeotropic composition which has new and unusual properties. Another object is to provide an azeotropic composition which is valuable as a solvent, and particularly for cleaning printed circuits. A further object is to provide such a composition which is nonflammable and nontoxic, both in the liquid phase and in the vapor phase. Other objects are to provide new compositions of matter and to advance the art. Still other objects will appear hereinafter.
The above and other objects may be accomplished in accord with this invention which comprises an azeotropic composition consisting of about 52% by weight of 1,1,2- trichloro-l,2,2atrifluoroethane and about 48% by weight of methylene chloride and boiling at 37 C. at 760 mm. pressure.
It has been found that l,1,2-trichloro-l,2,2-trifiuoroethane and methylene chloride (CH Cl when admixed in the above proportions form an azeotrope which distils at constant composition, the liquid phase and the vapor phase in equilibrium therewith having the same composition. Such mixture is nonflammable and nontoxic in both the liquid phase and the vapor phase. It is useful as a heat exchange medium and as a hydraulic fluid. It is particularly useful as a solvent for greases, oils, waxes, and the like, in cleaning electric motors, compressors, photographic film, oxygen storage tanks, lithographic, plates, typewriters, precision instruments, gauges, sound tape, components of engines which use liquid oxygen, and
2,999,817, Patented Sept. 12, 1961 printed circuits. The 1,1,2trichloro-1,2,2-trifluoroethane alone has insufiicient solvent power for many of such purposes, and the methylene chloride alone is objectionable for some of such purposes. It has been found that, in the azeotrope, the components modify the solvent properties of each other so that the azeotropic mixture is an excellent solvent for such purposes without having the disadvantages of either.
In the cleaning of components of engines which use liquid oxygen, it is particularly-important that the solvent remove alloxidizable materials so that they will not contact the liquid oxygen and that the solvent leave no residue which will react with liquid oxygen. The azeotropic mixture of this invention has the desired properties which render it useful for this pur'p'oseI r i The azeotropic mixture of l,l,2-trichloro-l,2,2-trifluoroethane and methylene chloride is of special value for cleaning printed circuits. The l, --l,2-trichloro-l,2,2- trifiuoroethane alone is'not an elfective' solvent for cleaning printed circuits, and has no deleteriousfefiect on the boards which form the bases of the printed circuits. Methylene chloride alone deleteriously ,aifects such boards, particularly laminated boards impregnated with phenolic resins, causing softening, swelling "and delamination of such boards and dissolving certain marking inks which are used to code various electronic components in the printed circuit assembly. The azeotropic mixture of this invention does not have these effects and is an excellent solvent for such purpose.
The azeotrope of this invention has several advantages over the solvents heretofore employed for cleaning printed circuits. Trichloroethylene, tetrachloroethylene, and methyl chloroform, are unstable and require stabilizers, whereas the azeotropic composition of this invention does not require a stabilizer, has a more favorable evaporation rate (is lower boiling), and is considerably less toxic than such solvents. The azeotropic composition of this invention is more effective as a solvent for such purposes than trichloroethylene and tetrachloroethylene. Inhibited methyl chloroform (containing dioxane as a stabilizer) is too strong a solvent and attacks the backing of the printed circuits. -Isopropyl alcohol-toluene blends are flammable and irritating. The azeotropic mixture of 1,l,Z-trichloro-1,2,2-trifluoroethane and methylene chloride does not suifer from any of these defects.
The azeotropic composition of this invention was established by the fractional distillation of a mixture containing 20% by weight'of l,l,2-trichloro-1,2,2-trifluoroethane and by weight of methylene chloride. The first fraction collected, amounting to 40% of the original mixture, was the azeotrope containing 52% by weight of 1,1,Z-trichloro-1,2,2-trifluoroethane and 48% by weight of methylene chloride having a boiling point of 37 C. at 760 mm. pressure, freezing point C. to 92 C., 11 1.3860. Distillation of mixtures of different proportions, eg 60% CCl- FCClF and 40% CH Cl always gave, as the first fraction, the azeotrope boiling at 37 C. The fractions boiling at 37 C. could be redisti-lled, giving material which boiled at 37 C. throughout with no separation into the components of the mixture.
Printed circuit boards are usually prepared by impregnating glass cloth, nylon, or paper laminates with a phenol-formaldehyde resin or an epoxy resin. Printed circuits are prepared by a variety of methods. In a typical procedure, the board consists originally of a phenolic resin impregnated base to which is bonded a sheet of copper, 2 to 4 mils thick, covering one surface of the board. The desired circuitis drawn on the copper with an asphalt based ink, using the silk screen method. The
excess copper is then removed by etching with a ferric chloride-hydrochloric acid bath, sometimes containing ammonium chloride, leaving on the board the copper that is covered by the ink. After washing 01f the etch solution, the asphalt ink is removed by cleaning with the azeotropic composition of this invention in an ultrasonic bath (some mechanical scrubbing is often used). The entire surface of the board is then coated with a rosin flux and dried. The electronic components (resistors, capacitors, etc.) are then added at the proper places for soldering to the circuit. The board is then passed over a molten solder bath, contacting the desired joints With the molten metal, whereby the soldering is effected. After cooling, the excess rosin flux remaining on the board must be removed since, if present in the final assembly, it will lead to corrosion, poor electrical resistance and other deleterious properties.
The board is cleaned by placing it in an ultrasonic bath operating at about 32 kilocycles per second and at about 25 C., where it remains for one minute. If 1,1,2-trichloro-1,2,2-trifluoroethane is used alone as the solvent in the bath, it has no effect on the rosin flux. If trichloroethylene is used as the solvent in the bath, about 5% to about 50% of the flux remains after the treatment. If the same cleaning operation is repeated on another circuit board using the azeotropic mixture of 1,1,2-trichloro- 1,2,2-trifluoroethane and methylene chloride as the solvent, the rosin fiux is completely removed. Neither the 1,1,2 trichloro-1,2,2-trifluoroethane nor the azeotropic mixture has any efiect on the board which constitutes the backing of the printed circuit.
It will be understood that the preceding detailed description of the use of the azeotropic composition of this invention in cleaning printed circuits is given for illustrative purposes solely, that this invention is not restricted to such specific embodiment, and that other techniques may be employed. Also, the azeotropic composition can be used for other purposes as indicated in the general description.
From the preceding description, it will be apparent that this invention provides a novel azeotropic composition which has unusual properties and which is useful for a wide variety of purposes. Accordingly, it will be apparent that invention constitutes a valuable contribution to and advance in the art.
The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
A11 azetropic composition consisting of about 52% by Weight of 1,1,2-trich1oro-1,2,2-trifluoroethane and about 48% by weight of methylene chloride and boiling at 37 C. and 760 mm. pressure.
References Cited in the file of this patent UNITED STATES PATENTS 2,155,510 Shepperd Apr. 25, 1939 2,547,887 Reed et a1 Apr. 3, 1951 2,911,331 Dennis et a1. Nov. 3, 1959 OTHER REFERENCES Industrial solvents, Mellan, 2nd ed. (1950), pp. 4879, 314-315, 372-373.
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Cited By (41)

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US3212998A (en) * 1962-12-06 1965-10-19 Dow Chemical Co Azeotropic distillation of bromine
US3282853A (en) * 1964-03-24 1966-11-01 Du Pont Azeotropic composition and process for attenuating magnetic ink characters
US3330776A (en) * 1964-12-08 1967-07-11 Du Pont Trichlorotrifluoroethane hexafluoropropanol composition
US3332881A (en) * 1964-12-21 1967-07-25 Du Pont Azeotropic composition
US3351560A (en) * 1965-04-09 1967-11-07 Dow Chemical Co Solvent composition
US3400077A (en) * 1965-12-22 1968-09-03 Allied Chem Fluorinated hydrocarbon containing compositions
FR2077227A1 (en) * 1970-01-20 1971-10-22 Hoechst Ag
US3625763A (en) * 1968-12-04 1971-12-07 Bunker Ramo Conformal coating stripping method and composition
US3846332A (en) * 1971-08-02 1974-11-05 Airco Inc Azeotropes of 1-chloro-2,2,2-trifluoroethyl difluoromethyl ether with acetone, methyl ethylketone and tetrahydrofuran
FR2231771A1 (en) * 1973-05-29 1974-12-27 Cerca Corrosion protection of uranium radiation shields - by cleaning surface then electrode positing nickel, zinc, cadmium or nickel-tin alloy
US3915875A (en) * 1973-03-23 1975-10-28 Mc Donnell Douglas Corp Low temperature fluid
US3951843A (en) * 1973-01-09 1976-04-20 Lfe Corporation Fluorocarbon composition for use in plasma removal of photoresist material from semiconductor devices
US4055521A (en) * 1975-10-08 1977-10-25 Allied Chemical Corporation Constant boiling ternary compositions and the process for using such compositions in the preparation of polyurethane foam
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US4476036A (en) * 1983-09-12 1984-10-09 Allied Corporation Quaternary 1,1,2-trichloro-1,2,2-trifluoro azeotropic cleaning composition
US4715900A (en) * 1987-01-08 1987-12-29 E. I. Du Pont De Nemours And Company Azeotropic compositions of trichlorotrifluoroethane, dichlorodifluoroethane and methanol/ethanol
US4808331A (en) * 1988-05-24 1989-02-28 E. I. Du Pont De Nemours And Company Azeotrope or azeotrope-like composition of 1,1,2,-trichloro-1,2,2-trifluoroethane, trans-1,2-dichloroethylene and cyclopentane
US4873021A (en) * 1986-12-30 1989-10-10 E. I. Du Pont De Nemours And Company Azeotrope or azeotrope-like composition of trichlorotrifluoroethane and dichlorodifluoroethane
US4954289A (en) * 1989-06-12 1990-09-04 E. I. Du Pont De Nemours And Company Azeotropes of hydrogen-containing halocarbons with butanes
US4986928A (en) * 1990-03-21 1991-01-22 E. I. Du Pont De Nemours And Company Binary azeotropic compositions of 1-chloro-1,2,2-trifluorocyclobutane and methanol
US4994202A (en) * 1990-03-12 1991-02-19 E. I. Du Pont De Nemours And Company Azeotropic compositions of perfluoro-1,2-dimethylcyclobutane with 1,1-dichloro-1-fluoroethane or dichlorotrifluoroethane
US5023009A (en) * 1990-10-03 1991-06-11 E. I. Du Pont De Nemours And Company Binary azeotropic compositions of 1,1,1,2,3,3-hexafluoro-3-methoxypropane and 2,2,3,3,3-pentafluoropropanol-1
US5026499A (en) * 1990-03-21 1991-06-25 E. I. Du Pont De Nemours And Company Ternary azeotropic compositions of hexafluoropropylene/ethylene cyclic dimer with trans-1,2-dichloroethylene and methanol
US5026497A (en) * 1990-03-12 1991-06-25 E. I. Du Pont De Nemours And Company Azeotropic compositions of perfluoro-1,2-dimethylcyclobutane with methanol and 1,1-dichloro-1-fluoroethane or dichlorotrifluoroethane
US5037572A (en) * 1990-10-03 1991-08-06 E. I. Du Pont De Nemours And Company Ternary azeotropic compositions of n-perfluorobutylethylene and trans-1,2-dichloroethylene with methanol or ethanol or isopropanol
US5037573A (en) * 1990-10-03 1991-08-06 E. I. Du Pont De Nemours And Company Binary azeotropic compositions of 1,1-dichloro-1-fluoroethane and n-perfluorobutylethylene
US5039445A (en) * 1990-10-03 1991-08-13 E. I. Du Pont De Nemours And Company Ternary azeotropic compositions of N-perfluorobutylethylene and cis-1,2-dichloroethylene with methanol or ethanol or isopropanol
US5066417A (en) * 1989-07-20 1991-11-19 E. I. Du Pont De Nemours And Company Binary azeotropic compositions of 2,2-dichloro-1,2-difluoroethane with methanol, ethanol, or trans-1,2-dichloroethylene
US5073288A (en) * 1990-08-17 1991-12-17 E. I. Du Pont De Nemours And Company Compositions of 1,1,1,2,2,3,5,5,5-nonafluoro-4-trifluoromethylpentane and use thereof for cleaning solid surfaces
US5073290A (en) * 1990-08-17 1991-12-17 E. I. Du Pont De Nemours And Company Compositions of 1,1,1,2,2,5,5,5-octafluoro-4-trifluormethypentane and use thereof for cleaning solid surfaces
US5076956A (en) * 1990-11-29 1991-12-31 E. I. Du Pont De Nemours And Company Compositions of octafluorotrifluoromethylpentane and nonafluorotrifluoromethylpentane and use thereof for cleaning solid surfaces
US5084199A (en) * 1990-03-05 1992-01-28 E. I. Du Pont De Nemours And Company 1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning
US5171902A (en) * 1990-10-11 1992-12-15 E. I. Du Pont De Nemours And Company Saturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions
US5176757A (en) * 1990-03-05 1993-01-05 E. I. Du Pont De Nemours And Company 1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning
US5221361A (en) * 1990-08-17 1993-06-22 E. I. Du Pont De Nemours And Company Compositions of 1,1,1,2,2,5,5,5,-octafluoro-4-trifluoromethylpentane and use thereof for cleaning solid surfaces
US5240634A (en) * 1990-03-12 1993-08-31 E. I. Du Pont De Nemours And Company Ternary azeotropic compositions of 1,1-dichloro-1,2-difluoroethane and cis-1,2-dichloroethylene with methanol or ethanol or n-propanol
US5250213A (en) * 1991-05-06 1993-10-05 E. I. Du Pont De Nemours And Company 1,1,1,2,2,3,3,4,4,5,6-undecafluorohexane and use thereof in compositions and processes for cleaning
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US6030934A (en) * 1997-02-19 2000-02-29 3M Innovative Properties Company Azeotropic compositions of methoxy-perfluoropropane and their use
US8592538B2 (en) 2011-12-20 2013-11-26 Honeywell International Inc. Azeotropes of methyl chloride with fluorocarbons

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US3663255A (en) * 1969-12-01 1972-05-16 Dow Chemical Co Composition containing chlorinated hydrocarbons ketones and glycol ethers, for reflowing organic surfaces
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US3951843A (en) * 1973-01-09 1976-04-20 Lfe Corporation Fluorocarbon composition for use in plasma removal of photoresist material from semiconductor devices
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US5176757A (en) * 1990-03-05 1993-01-05 E. I. Du Pont De Nemours And Company 1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning
US5084199A (en) * 1990-03-05 1992-01-28 E. I. Du Pont De Nemours And Company 1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning
US5240634A (en) * 1990-03-12 1993-08-31 E. I. Du Pont De Nemours And Company Ternary azeotropic compositions of 1,1-dichloro-1,2-difluoroethane and cis-1,2-dichloroethylene with methanol or ethanol or n-propanol
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US5221361A (en) * 1990-08-17 1993-06-22 E. I. Du Pont De Nemours And Company Compositions of 1,1,1,2,2,5,5,5,-octafluoro-4-trifluoromethylpentane and use thereof for cleaning solid surfaces
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US5037573A (en) * 1990-10-03 1991-08-06 E. I. Du Pont De Nemours And Company Binary azeotropic compositions of 1,1-dichloro-1-fluoroethane and n-perfluorobutylethylene
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US5723701A (en) * 1990-10-11 1998-03-03 E. I. Du Pont De Nemours And Company Saturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions
US5171902A (en) * 1990-10-11 1992-12-15 E. I. Du Pont De Nemours And Company Saturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions
US5504265A (en) * 1990-10-11 1996-04-02 E. I. Du Pont De Nemours And Company Saturated linear polyfluorohydrocarbons, processes for their production, and their use in cleaning compositions
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