US3671444A - Azeotropic composition - Google Patents
Azeotropic composition Download PDFInfo
- Publication number
- US3671444A US3671444A US54084A US3671444DA US3671444A US 3671444 A US3671444 A US 3671444A US 54084 A US54084 A US 54084A US 3671444D A US3671444D A US 3671444DA US 3671444 A US3671444 A US 3671444A
- Authority
- US
- United States
- Prior art keywords
- tetrachlorodifluoroethane
- azeotropes
- methanol
- butanol
- ethanol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000000203 mixture Substances 0.000 title claims abstract description 30
- 238000004140 cleaning Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract description 39
- 239000002904 solvent Substances 0.000 abstract description 27
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 22
- SLGOCMATMKJJCE-UHFFFAOYSA-N 1,1,1,2-tetrachloro-2,2-difluoroethane Chemical compound FC(F)(Cl)C(Cl)(Cl)Cl SLGOCMATMKJJCE-UHFFFAOYSA-N 0.000 abstract description 17
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract description 16
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract description 10
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 abstract description 8
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 abstract description 6
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 abstract description 6
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 abstract description 6
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 abstract description 5
- 238000009835 boiling Methods 0.000 description 10
- 230000004907 flux Effects 0.000 description 7
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 6
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 238000005238 degreasing Methods 0.000 description 4
- 239000013527 degreasing agent Substances 0.000 description 4
- 231100000252 nontoxic Toxicity 0.000 description 4
- 230000003000 nontoxic effect Effects 0.000 description 4
- YACLCMMBHTUQON-UHFFFAOYSA-N 1-chloro-1-fluoroethane Chemical class CC(F)Cl YACLCMMBHTUQON-UHFFFAOYSA-N 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- 239000012808 vapor phase Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 239000010426 asphalt Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- -1 fluoroethane Methanol Ethanol Chemical compound 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 229910000679 solder Inorganic materials 0.000 description 2
- 238000005476 soldering Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- BTANRVKWQNVYAZ-SCSAIBSYSA-N (2R)-butan-2-ol Chemical compound CC[C@@H](C)O BTANRVKWQNVYAZ-SCSAIBSYSA-N 0.000 description 1
- UGCSPKPEHQEOSR-UHFFFAOYSA-N 1,1,2,2-tetrachloro-1,2-difluoroethane Chemical compound FC(Cl)(Cl)C(F)(Cl)Cl UGCSPKPEHQEOSR-UHFFFAOYSA-N 0.000 description 1
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000011101 paper laminate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G5/00—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
- C23G5/02—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
- C23G5/028—Cleaning 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
- C23G5/02809—Cleaning 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
- C23G5/02812—Perhalogenated hydrocarbons
- C23G5/02816—Ethanes
- C23G5/02822—C2Cl4F2
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5036—Azeotropic mixtures containing halogenated solvents
- C11D7/5068—Mixtures of halogenated and non-halogenated solvents
- C11D7/5077—Mixtures of only oxygen-containing solvents
- C11D7/5081—Mixtures of only oxygen-containing solvents the oxygen-containing solvents being alcohols only
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G5/00—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
- C23G5/02—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
-
- C—CHEMISTRY; METALLURGY
- C23—COATING 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
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G5/00—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
- C23G5/02—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
- C23G5/028—Cleaning 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
- C23G5/02806—Cleaning 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 only chlorine as halogen atom
Definitions
- the disclosure relates to binary azeotropic mixtures of tetrachlorodifluoroethane and methanol. 1! has also been discovered that n-butanol or isobutanol or sec-butanol will form azeotropes with these halogenated solvents.
- the disclosure also relates to ternary azeotropes of tetrachlorodifluoroethane and trichloroethylene with methanol. It has also been discovered that ethanol or isopropanol will also form ternary azeotropes with these two halogenated solvents.
- ternary azeotropes comprising tetrachlorodifluoroethane, trichloroethane and methanol. It has also been discovered that ethanol and isopropanol will also form ternary azeotropes with these two halogenated solvents.
- This invention relates to an azeotropic composition and particularly to the binary and ternary azeotropic mixture of tetrachlorodifluoroethane and methanol or any one of the isomers, n-butanol or iso-butanol or sec.-butanol.
- the present invention also relates to ternary azeotropes of tetrachlorodifluoroethane and trichloroethylene with either methanol or ethanol or isopropanol.
- ternary azeotropes have been discovered comprising tetrachlorodifluoro-ethane, trichloroethane and either methanol or ethanol or isopropanol. 1
- chlorofluoroethanes have attained widespread use as specialty solvents in recent years, particularly tetrachlorodifluoroethane.
- This is a relatively high melting compound (CCl FCCl F, 24.5 C.), which is nontoxic and nonflammable, and which has satisfactory solvent power for greases, oils, waxes and the like under certain conditions. It has therefore found use in cleaning electric motors, compressors, lithographic plates, typewriters, instruments, gauges, and as non-corrosive brines.
- Printed cicuits are well known in the electronics art; and consist of a circuit formed from a soft metal on a solid, non-conducting surface such as a reinforced phenolic 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 impervious coating is removed, the circuits are coated with a rosin flux to permit the joints to be soldered, after which the rosin flux must then be removed.
- the chlorofluoroethane solvent does not have sufficient solvent power to clean printed circuits; that is, to effectively remove the rosin flux.
- mixtures of solvents may be used for this purpose they have the disadvantage that they boil over a range of temperatures and consequently undergo fractionation in vapor degreasing or ultrasonic applications which are open to the atmosphere.
- the solvent When employing either of these cleaning or degreasing methods the solvent must also be both relatively nontoxic and nonflammable for safety reasons.
- Tetrachlorodifluoroethane is a relatively high boiling fluorocarbon and for this reason is especially advantageous in vapor degreasing applications since at these temperatures the hot vapor has more of atend'ency to dissolve high melting greases, or fluxes as well as oil residues and the like.
- the solvent vapors tend to condense on the article until the articles are heated by the vapors from room temperature up to the temperature of the vapor. The condensation thus formed on the articles tends to drip back into the solvent reservoir taking with it some of the soil on the article. For this reason the ability of a cleaning solvent to condense on the surface is especially advantageous.
- Tetrachlorodifluoroethane also is a better solvent than materials such as trichlorotrifluoromethane, however, it suffers the disadvantage that it is solidus at room temperature whereas the latter is liquidus. Accordingly tetrachlorodifluoroethane is more difficult to handle than I liquid'type cleaning solvents.
- the above object of this invention may be accomplished by a novel binary azeotropic composition of tetrachlorodifluoroethane (e.g., l l ,2,2,-tetrachlorol .2- difluoroethane) and either methanol or n-butanol or secondary butanol or iso-butanol; ternary azeotropes of tetrachlorodifluoroethane (e.g., 1,1 ,2,2-tetrachloro- 1 ,2- difluoroethane) trichloroethylene and either methanol or ethanol or isopropanol; and ternary azeotropes of tetrachlorodifluoroethane e.g., l, l ,2,2-tetrachlorol ,2-
- trichloroethane e.g., l,l,l-trichloroethane
- methanol or ethanol or isopropanol e.g., 1,l,2,2-tetrachloro-l,2-difluoroethane
- the isomer 1 l l ,2-tetrachloro-2,2- difluoroethane may be substituted therefore in whole or in part and especially in minor amounts or trace amounts.
- the preferred trichloroethane comprises the 1,1 ,l-trichloroethane isomer.
- All of these mixtures form azeotropes which distill at a constant temperature, the liquid phase and the vapor phase in equilibrium therewith having the same composition.
- Such mixture is relatively nonflammable and nontoxic in both the liquid phase and the vapor phase.
- These mixtures are particularly useful as solvents for greases, oils, waxes, and the like and cleaning electric motors, compressors, lithographic plates, typewriters precision instruments, gauges,-and the like and are particularly useful for cleaning printed circuits.
- the azeotropic mixtures are obtained at approximately 760 mm Hg a variation in pressure and consequently a change in the compositions and boiling points are also intended to be within the boardscope of the invention.
- the azeotropes may contain many different proportions of all of the aforementioned components provided a constant boiling mixture is obtained at the various pressures at which the compositions are used. Stated otherwise any pressure may be employed to obtain the azeotropes of this invention as long as a three component or two component constant boiling mixture is obtained, and accordingly the ratio of components of the azeotropes of the invention will also vary.
- the present invention relates to the aforementioned azeotropes that boil at atmospheric pressure 1 about 25, especially about 15 mm Hg.
- the desired circuit is 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.
- 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 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 32 kilocycles per second-at about l0-20 F. below the boiling point of the particular azeotrope for about 1 minute.
- An azeotropic composition consisting essentially of about 36 parts, by weight, of l,l,2,2-tetrachloro-l,Z-difluoroethane, about 26 parts ethanol and about 38 parts trichloroethylene.
- a method for cleaning a solid surface comprising contacting said surface with the composition of claim 1.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Detergent Compositions (AREA)
- Manufacturing Of Printed Wiring (AREA)
Abstract
It is not intended that the following abstract of the disclosure be construed as limiting the invention in any manner. The disclosure relates to binary azeotropic mixtures of tetrachlorodifluoroethane and methanol. It has also been discovered that n-butanol or isobutanol or sec-butanol will form azeotropes with these halogenated solvents. The disclosure also relates to ternary azeotropes of tetrachlorodifluoroethane and trichloroethylene with methanol. It has also been discovered that ethanol or isopropanol will also form ternary azeotropes with these two halogenated solvents. In a further embodiment ternary azeotropes are disclosed comprising tetrachlorodifluoroethane, trichloroethane and methanol. It has also been discovered that ethanol and isopropanol will also form ternary azeotropes with these two halogenated solvents.
Description
United States Patent Schoiield et al.
[ 1 June 20, 1972 [54] AZEOTROPIC COMPOSITION [72] Inventors: J. Allan Schofleld, lrvington; Roger A.
Delano, Dobbs Ferry, both of NY.
52 us. Cl. .252 171, 252/66, 252 010. 9 51 ..Clld 7 50, C23g 5/02 581 ..252/l7l,66-68,
[56] References Cited UNITED STATES PATENTS 3,085,1l6 4/l963 Kvalnes ..260/652.5 3,285,858 ll/l966 Hirschetal ..252/l7l Primary Examiner-Leon D. Rosdol Assistant Examiner-W. Schulz Attorney-Paul A. Rose, Aldo .l. Cozzi, Vincent P. Pirri and Robert C. Brown [57] ABSTRACT It is not intended that the following abstract of the disclosure be construed as limiting the invention in any manner.
The disclosure relates to binary azeotropic mixtures of tetrachlorodifluoroethane and methanol. 1! has also been discovered that n-butanol or isobutanol or sec-butanol will form azeotropes with these halogenated solvents.
The disclosure also relates to ternary azeotropes of tetrachlorodifluoroethane and trichloroethylene with methanol. It has also been discovered that ethanol or isopropanol will also form ternary azeotropes with these two halogenated solvents.
In a further embodiment ternary azeotropes are disclosed comprising tetrachlorodifluoroethane, trichloroethane and methanol. It has also been discovered that ethanol and isopropanol will also form ternary azeotropes with these two halogenated solvents.
3 Claims, No Drawings AZEOTROPIC COMPOSITION This is a division of application, Ser. No. 677,715 filed Oct. 24, 1967 now U.S. Pat. No. 3,554,918.
This invention relates to an azeotropic composition and particularly to the binary and ternary azeotropic mixture of tetrachlorodifluoroethane and methanol or any one of the isomers, n-butanol or iso-butanol or sec.-butanol. The present invention also relates to ternary azeotropes of tetrachlorodifluoroethane and trichloroethylene with either methanol or ethanol or isopropanol. In a further embodiment ternary azeotropes have been discovered comprising tetrachlorodifluoro-ethane, trichloroethane and either methanol or ethanol or isopropanol. 1
Several of the chlorofluoroethanes have attained widespread use as specialty solvents in recent years, particularly tetrachlorodifluoroethane. This is a relatively high melting compound (CCl FCCl F, 24.5 C.), which is nontoxic and nonflammable, and which has satisfactory solvent power for greases, oils, waxes and the like under certain conditions. It has therefore found use in cleaning electric motors, compressors, lithographic plates, typewriters, instruments, gauges, and as non-corrosive brines.
For certain solvent purposes however, the chlorofluoroethanes alone have insufficient solvent power. This is particularly true in the electronic industry during the manufacture of printed circuits." Printed cicuits are well known in the electronics art; and consist of a circuit formed from a soft metal on a solid, non-conducting surface such as a reinforced phenolic 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 impervious coating is removed, the circuits are coated with a rosin flux to permit the joints to be soldered, after which the rosin flux must then be removed.
The chlorofluoroethane solvent does not have sufficient solvent power to clean printed circuits; that is, to effectively remove the rosin flux. Although mixtures of solvents may be used for this purpose they have the disadvantage that they boil over a range of temperatures and consequently undergo fractionation in vapor degreasing or ultrasonic applications which are open to the atmosphere. When employing either of these cleaning or degreasing methods the solvent must also be both relatively nontoxic and nonflammable for safety reasons.
Tetrachlorodifluoroethane is a relatively high boiling fluorocarbon and for this reason is especially advantageous in vapor degreasing applications since at these temperatures the hot vapor has more of atend'ency to dissolve high melting greases, or fluxes as well as oil residues and the like. When articles such as circuit boards are passed through a vapor degreaser, the solvent vapors tend to condense on the article until the articles are heated by the vapors from room temperature up to the temperature of the vapor. The condensation thus formed on the articles tends to drip back into the solvent reservoir taking with it some of the soil on the article. For this reason the ability of a cleaning solvent to condense on the surface is especially advantageous. Higher boiling solvents prolong this condensation effect in a continuous degreaser since it takes a greater amount of time to bring the article passing through the degreaser up to the vapor temperature of the solvent. Consequently higher boiling solvents generally have better cleaning power per unit of time in a continuous vapor degreaser than the lower boiling solvents.
Tetrachlorodifluoroethane also is a better solvent than materials such as trichlorotrifluoromethane, however, it suffers the disadvantage that it is solidus at room temperature whereas the latter is liquidus. Accordingly tetrachlorodifluoroethane is more difficult to handle than I liquid'type cleaning solvents.
It is an object of this invention to provide a constant boiling or azeotropic solvent that is a liquid at room temperature, will not fractionate and also has the foregoing advantages' 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 an azeotropic composition which is both relatively nontoxic and n'onflammable both in the liquid phase and in the vapor phase and which at the same time is an excellent solvent for cleaning printed circuits especially by means of a continuous vapor degreasing machine. I
The above object of this invention may be accomplished by a novel binary azeotropic composition of tetrachlorodifluoroethane (e.g., l l ,2,2,-tetrachlorol .2- difluoroethane) and either methanol or n-butanol or secondary butanol or iso-butanol; ternary azeotropes of tetrachlorodifluoroethane (e.g., 1,1 ,2,2-tetrachloro- 1 ,2- difluoroethane) trichloroethylene and either methanol or ethanol or isopropanol; and ternary azeotropes of tetrachlorodifluoroethane e.g., l, l ,2,2-tetrachlorol ,2-
difluoroethane), trichloroethane (e.g., l,l,l-trichloroethane) and either methanol or ethanol or isopropanol. Although 1,l,2,2-tetrachloro-l,2-difluoroethane is a preferred tetrachlorodifluoroethane, the isomer 1 l l ,2-tetrachloro-2,2- difluoroethane may be substituted therefore in whole or in part and especially in minor amounts or trace amounts. The preferred trichloroethane comprises the 1,1 ,l-trichloroethane isomer. All of these mixtures form azeotropes which distill at a constant temperature, the liquid phase and the vapor phase in equilibrium therewith having the same composition. Such mixture is relatively nonflammable and nontoxic in both the liquid phase and the vapor phase. These mixtures are particularly useful as solvents for greases, oils, waxes, and the like and cleaning electric motors, compressors, lithographic plates, typewriters precision instruments, gauges,-and the like and are particularly useful for cleaning printed circuits.
Although the azeotropic mixtures are obtained at approximately 760 mm Hg a variation in pressure and consequently a change in the compositions and boiling points are also intended to be within the boardscope of the invention. Thus the azeotropes may contain many different proportions of all of the aforementioned components provided a constant boiling mixture is obtained at the various pressures at which the compositions are used. Stated otherwise any pressure may be employed to obtain the azeotropes of this invention as long as a three component or two component constant boiling mixture is obtained, and accordingly the ratio of components of the azeotropes of the invention will also vary. The variation of components is thus within the skill of the art and is easily determined once it is known that the halogenated hydrocarbons of this invention will form the aforementioned azeotropes. In a preferred embodiment the present invention relates to the aforementioned azeotropes that boil at atmospheric pressure 1 about 25, especially about 15 mm Hg.
EXAMPLE I Components Composition Percent Boiling Point, by Weight F. 760 mm Hg 1, l ,2,2-tetrachlorol ,2-difluoroethane 69.3 140 methanol 30.7
EXAMPLES ll-X The method of Example I is repeated using different mixtures of alcohols and/or l,l,l-trichloroethane or trichloroethylene and l, l ,2,2,-tetrachlorol ,2,- difluoroethane, the results of which are as follows:
COMPONENTS, PERCENT BY WEIGHT 1,1,12,2-tetta- 1,1,1-tri- Example ch1or0-12-di- Trichlorochloro- Bolling mm. Hg. number fluoroethane Methanol Ethanol l-Propanol n-Butanol l-Butanol s-Butanol ethylene ethane point, F. pressure Printed circuit boards are usually prepared by impregnating glass cloth, nylon, or paper laminates with a phenolformaldehyde resin or an epoxy resin. Printed circuits are prepared by a variety of methods. In a typical procedure, the board consists originally ofa 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 circuit is 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 0E 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 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 32 kilocycles per second-at about l0-20 F. below the boiling point of the particular azeotrope for about 1 minute.
When the board is cleaned with the azeotropic mixtures of this invention substantially all of the rosin flux is removed without any detrimental effect on the board which constitutes the backing of the printed circuit.
Although the invention has been described by reference to some preferred embodiments it is not intended that the broad scope of the novel azeotropic compositions be limited thereby but that certain modifications are intended to be included within the spirit and broad scope of the following claims.
What is claimed is:
1. An azeotropic composition consisting essentially of about 36 parts, by weight, of l,l,2,2-tetrachloro-l,Z-difluoroethane, about 26 parts ethanol and about 38 parts trichloroethylene.
2. A method for cleaning a solid surface comprising contacting said surface with the composition of claim 1.
3. A method in accordance with claim 2 wherein said composition is in vapor form.
Claims (2)
- 2. A method for cleaning a solid surface comprising contacting said surface with the composition of claim 1.
- 3. A method in accordance with claim 2 wherein said composition is in vapor form.
Applications Claiming Priority (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US67771567A | 1967-10-24 | 1967-10-24 | |
US5408670A | 1970-06-02 | 1970-06-02 | |
US5408470A | 1970-06-02 | 1970-06-02 | |
US5408170A | 1970-06-02 | 1970-06-02 | |
US5408370A | 1970-06-02 | 1970-06-02 | |
US5408570A | 1970-06-02 | 1970-06-02 | |
US5408270A | 1970-06-02 | 1970-06-02 | |
US00255972A US3833507A (en) | 1967-10-24 | 1972-05-23 | Azeotropic composition |
Publications (1)
Publication Number | Publication Date |
---|---|
US3671444A true US3671444A (en) | 1972-06-20 |
Family
ID=27574375
Family Applications (8)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US677715D Pending USB677715I5 (en) | 1967-10-24 | ||
US677715A Expired - Lifetime US3554918A (en) | 1967-10-24 | 1967-10-24 | Azeotropic composition |
US54081A Expired - Lifetime US3671442A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
US54084A Expired - Lifetime US3671444A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
US54086A Expired - Lifetime US3671445A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
US54082A Expired - Lifetime US3671443A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
US54085A Expired - Lifetime US3671446A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
US00255972A Expired - Lifetime US3833507A (en) | 1967-10-24 | 1972-05-23 | Azeotropic composition |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US677715D Pending USB677715I5 (en) | 1967-10-24 | ||
US677715A Expired - Lifetime US3554918A (en) | 1967-10-24 | 1967-10-24 | Azeotropic composition |
US54081A Expired - Lifetime US3671442A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
Family Applications After (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US54086A Expired - Lifetime US3671445A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
US54082A Expired - Lifetime US3671443A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
US54085A Expired - Lifetime US3671446A (en) | 1967-10-24 | 1970-06-02 | Azeotropic composition |
US00255972A Expired - Lifetime US3833507A (en) | 1967-10-24 | 1972-05-23 | Azeotropic composition |
Country Status (2)
Country | Link |
---|---|
US (8) | US3554918A (en) |
CA (1) | CA955820A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3936387A (en) * | 1972-02-04 | 1976-02-03 | Phillips Petroleum Company | Azeotrope of 1,2-dichloro-1-fluoroethane and methanol |
US4035258A (en) * | 1973-08-27 | 1977-07-12 | Phillips Petroleum Company | Azeotropic compositions |
US4169807A (en) * | 1978-03-20 | 1979-10-02 | Rca Corporation | Novel solvent drying agent |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4023984A (en) * | 1973-02-02 | 1977-05-17 | Imperial Chemical Industries Limited | Azeotropic solvent composition for cleaning |
US3957530A (en) * | 1973-03-06 | 1976-05-18 | Phillips Petroleum Company | Ternary azeotropic paint stripping compositions |
US3904542A (en) * | 1973-03-06 | 1975-09-09 | Phillips Petroleum Co | Azeotropic composition of fluorocarbon |
JPS5958099A (en) * | 1982-09-27 | 1984-04-03 | ダイキン工業株式会社 | cleaning composition |
NO834067L (en) * | 1982-11-08 | 1984-05-09 | Dow Chemical Co | SOLVENT MIXTURE TO REMOVE FLUID |
US4524011A (en) * | 1982-11-08 | 1985-06-18 | The Dow Chemical Company | Flux removal solvent blend |
JPS61190596A (en) * | 1985-02-20 | 1986-08-25 | ダイキン工業株式会社 | azeotrope-like composition |
DE3702399A1 (en) * | 1987-01-28 | 1988-08-11 | Kali Chemie Ag | NEW MIXTURES WITH DIFLUORTETRACHLORAETHANE |
US5514221A (en) * | 1993-04-15 | 1996-05-07 | Elf Atochem North America, Inc. | Cold cleaning process |
US5552080A (en) * | 1993-04-15 | 1996-09-03 | Elf Atochem North America, Inc. | Cold cleaning solvents |
US6342471B1 (en) * | 2000-01-25 | 2002-01-29 | Toney M. Jackson | Electrical contact cleaner |
FR2855069B1 (en) * | 2003-05-22 | 2006-06-16 | Solvay | PROCESS FOR THE SEPARATION OF AT LEAST ONE ORGANIC COMPOUND |
-
0
- US US677715D patent/USB677715I5/en active Pending
-
1967
- 1967-10-24 US US677715A patent/US3554918A/en not_active Expired - Lifetime
-
1968
- 1968-08-13 CA CA027,298A patent/CA955820A/en not_active Expired
-
1970
- 1970-06-02 US US54081A patent/US3671442A/en not_active Expired - Lifetime
- 1970-06-02 US US54084A patent/US3671444A/en not_active Expired - Lifetime
- 1970-06-02 US US54086A patent/US3671445A/en not_active Expired - Lifetime
- 1970-06-02 US US54082A patent/US3671443A/en not_active Expired - Lifetime
- 1970-06-02 US US54085A patent/US3671446A/en not_active Expired - Lifetime
-
1972
- 1972-05-23 US US00255972A patent/US3833507A/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3936387A (en) * | 1972-02-04 | 1976-02-03 | Phillips Petroleum Company | Azeotrope of 1,2-dichloro-1-fluoroethane and methanol |
US4035258A (en) * | 1973-08-27 | 1977-07-12 | Phillips Petroleum Company | Azeotropic compositions |
US4169807A (en) * | 1978-03-20 | 1979-10-02 | Rca Corporation | Novel solvent drying agent |
Also Published As
Publication number | Publication date |
---|---|
US3671442A (en) | 1972-06-20 |
US3671446A (en) | 1972-06-20 |
CA955820A (en) | 1974-10-08 |
US3671443A (en) | 1972-06-20 |
US3554918A (en) | 1971-01-12 |
US3833507A (en) | 1974-09-03 |
US3671445A (en) | 1972-06-20 |
USB677715I5 (en) |
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