US3833507A - Azeotropic composition - Google Patents

Azeotropic composition Download PDF

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Publication number
US3833507A
US3833507A US00255972A US25597272A US3833507A US 3833507 A US3833507 A US 3833507A US 00255972 A US00255972 A US 00255972A US 25597272 A US25597272 A US 25597272A US 3833507 A US3833507 A US 3833507A
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Prior art keywords
solvent
azeotropic composition
cleaning
tetrachloro
vapor
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US00255972A
Inventor
J Schofield
R Delano
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Lyondell Chemical Technology LP
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Union Carbide Corp
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Publication date
Priority to US677715D priority Critical patent/USB677715I5/en
Priority to US677715A priority patent/US3554918A/en
Priority to CA027,298A priority patent/CA955820A/en
Priority to US54084A priority patent/US3671444A/en
Priority to US54082A priority patent/US3671443A/en
Priority to US54085A priority patent/US3671446A/en
Priority to US54081A priority patent/US3671442A/en
Priority to US54086A priority patent/US3671445A/en
Priority to US00255972A priority patent/US3833507A/en
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Application granted granted Critical
Publication of US3833507A publication Critical patent/US3833507A/en
Assigned to MORGAN GUARANTY TRUST COMPANY OF NEW YORK, AND MORGAN BANK ( DELAWARE ) AS COLLATERAL ( AGENTS ) SEE RECORD FOR THE REMAINING ASSIGNEES. reassignment MORGAN GUARANTY TRUST COMPANY OF NEW YORK, AND MORGAN BANK ( DELAWARE ) AS COLLATERAL ( AGENTS ) SEE RECORD FOR THE REMAINING ASSIGNEES. MORTGAGE (SEE DOCUMENT FOR DETAILS). Assignors: STP CORPORATION, A CORP. OF DE.,, UNION CARBIDE AGRICULTURAL PRODUCTS CO., INC., A CORP. OF PA.,, UNION CARBIDE CORPORATION, A CORP.,, UNION CARBIDE EUROPE S.A., A SWISS CORP.
Assigned to UNION CARBIDE CORPORATION, reassignment UNION CARBIDE CORPORATION, RELEASED BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: MORGAN BANK (DELAWARE) AS COLLATERAL AGENT
Assigned to ARCO CHEMICAL TECHNOLOGY, INC. reassignment ARCO CHEMICAL TECHNOLOGY, INC. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: UNION CARBIDE CHEMICALS AND PLASTICS COMPANY, INC.
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • 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
    • C23G5/02822C2Cl4F2
    • 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
    • C11D7/5068Mixtures of halogenated and non-halogenated solvents
    • C11D7/5077Mixtures of only oxygen-containing solvents
    • C11D7/5081Mixtures of only oxygen-containing solvents the oxygen-containing solvents being alcohols only
    • 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
    • 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
    • C23G5/02806Cleaning 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

  • This invention relates to an azeotropic composition of a tetrachlorodifiuoroethane, methanol and trichloroethylene.
  • chlorofluoroethanes have attained widespread use as specialty solvents in recent years, particularly tetrachlorodifiuoroethane.
  • This is a relatively high melting compound (CCI 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 noncorrosive brines.
  • Printed circuits 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 sufiicient 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 a tendency 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 3,833,507 Patented Sept. 3, 1974 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 difiicult to handle than liquid type cleaning solvents.
  • the above object of this invention may be accomplished by a novel ternary azeotropic composition of tetrachlorodifiuoroethane (e.g. 1,1,2,2-tetrachloro 1,2 difluoroethane), methanol and trichloroethylene.
  • 1,1,2,2-tetrachloro 1,2 difluoroethane is the preferred tetrachlorodifluoroethane
  • the isomer 1,1,1,2 tetrachloro-2,2-difluoroethane may be substituted therefor in whole or in part and especially in minor amounts or trace amounts.
  • the ternary azeotrope of this invention is unusual but not unique among ternary azeotropes in that the proportions of the three elements of the azeotrope can vary to appreciable extent.
  • the permissible variations in the azeotrope, Without an appreciable change in boiling point are as follows:
  • compositions Percent by weight 1,1,2,2 tetrachloro 1,2 difiuoroethane 34-41 Methanol 30 Trichloroethylene 36-29 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 nonfiammable 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 broad scope of the invention.
  • the azeotropes may contain many ditferent 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 i about 25, especially 1 about 15 mm. Hg.
  • Example II Repeating the procedure of Example I, beginning with a mixture of equal amounts of each of the three components an azeotropic mixture which has a constant boiling point of 140 F. at 760 mm. Hg consisting essentially of 34.3 percent l,1,2,2-tetrachloro-1,2-difluoroethane, 30.1 percent methanol and 35.6 percent trichloroethylene by weight.
  • 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 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 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 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 of any of the aforementioned azeotropes and operating at about 32 kilocycles per second at about 10-20 F. below the boiling point of the particular azeotrope for about one minute.
  • An azeotropic composition consisting essentially of from about 34 to 41 parts by weight of l,1,2,2-tetrachloro- 1,2-difluoroethane, about 30 parts methanol and from about 36 to 29 parts trichloroethylene.
  • An azeotropic composition consisting essentially of about 34 parts by Weight of 1,1,2,2-tetrachloro-1,2-difluoroethane, about 30 parts methanol and about 36 parts trichloroethylene.
  • An azeotropic composition consisting essentially of about 40 parts by weight of 1,1,2,2-tetrachloro-1,2-difiuoroethane, about 30 parts methanol and about 30 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

A TERNARY AZEOTROPE OF 1,1,2,2-TRETRACHLORO-1,2-DIFLUOROETHANE, METHANOL AND TRICHLOROETHYLENE.

Description

3,833,507 AZEGTROPIC COMPOSITION J. Allan Schofield, Riverside, Conn., and Roger A. Delano,
Dobbs Ferry, N.Y., assignors to Union Carbide Corporation, New York, N.Y. No Drawing. Continuation-impart of abandoned applications Ser. No. 54,083, June 2, 1970, and Ser. No. 677,715, Oct. 24, 1967. This application May 23, 1972, Ser. No. 255,972
Int. Cl. Clld 7/50 U.S. Cl. 252-171 Claims ABSTRACT OF THE DISCLOSURE A ternary azeotrope of 1,1,2,2-tetrachloro-1,2-difluoroethane, methanol and trichloroethylene.
This application is a continuation-in-part of application Ser. No. 54,083 filed June 2, 1970 and application Ser. No. 677,715 filed Oct. 24, 1967 and both now abandoned.
This invention relates to an azeotropic composition of a tetrachlorodifiuoroethane, methanol and trichloroethylene.
Several of the chlorofluoroethanes have attained widespread use as specialty solvents in recent years, particularly tetrachlorodifiuoroethane. This is a relatively high melting compound (CCI 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 noncorrosive 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 circuits 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 sufiicient 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 a tendency 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 3,833,507 Patented Sept. 3, 1974 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 difiicult to handle than 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 printing circuits. A further object is to provide an azeotropic composition which is both relatively nontoxic and nonflammable 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.
The above object of this invention may be accomplished by a novel ternary azeotropic composition of tetrachlorodifiuoroethane (e.g. 1,1,2,2-tetrachloro 1,2 difluoroethane), methanol and trichloroethylene. Although 1,1,2,2-tetrachloro 1,2 difluoroethane is the preferred tetrachlorodifluoroethane, the isomer 1,1,1,2 tetrachloro-2,2-difluoroethane may be substituted therefor in whole or in part and especially in minor amounts or trace amounts.
The ternary azeotrope of this invention is unusual but not unique among ternary azeotropes in that the proportions of the three elements of the azeotrope can vary to appreciable extent. The permissible variations in the azeotrope, Without an appreciable change in boiling point are as follows:
Components: Percent by weight 1,1,2,2 tetrachloro 1,2 difiuoroethane 34-41 Methanol 30 Trichloroethylene 36-29 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 nonfiammable 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 broad scope of the invention. Thus the azeotropes may contain many ditferent 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 a'zeotropes. In a preferred embodiment the present invention relates to the aforementioned azeotropes that boil at atmospheric pressure i about 25, especially 1 about 15 mm. Hg.
EXAMPLE I Cornp Boiling sition point,
percent F. 760
Components by weight mm. Hg
1,1,2,2-tetrachloro-l,2-difluoroethane 40. 2 140 Methanol 30. 3 Triehloroethylene 29. 5
EXAMPLE II Repeating the procedure of Example I, beginning with a mixture of equal amounts of each of the three components an azeotropic mixture which has a constant boiling point of 140 F. at 760 mm. Hg consisting essentially of 34.3 percent l,1,2,2-tetrachloro-1,2-difluoroethane, 30.1 percent methanol and 35.6 percent trichloroethylene by weight.
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 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 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 oif 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 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 of any of the aforementioned azeotropes and operating at about 32 kilocycles per second at about 10-20 F. below the boiling point of the particular azeotrope for about one minute.
When the board is cleaned with the azeotropic mixture of this invention substantially all of the rosin flux is removed without any detrimental eifect 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 composition be limited thereby but that certain modifications are intended to be included within the spirit and broad scope of the following claims.
We claim:
1. An azeotropic composition consisting essentially of from about 34 to 41 parts by weight of l,1,2,2-tetrachloro- 1,2-difluoroethane, about 30 parts methanol and from about 36 to 29 parts trichloroethylene.
2. An azeotropic composition consisting essentially of about 34 parts by Weight of 1,1,2,2-tetrachloro-1,2-difluoroethane, about 30 parts methanol and about 36 parts trichloroethylene.
3. An azeotropic composition consisting essentially of about 40 parts by weight of 1,1,2,2-tetrachloro-1,2-difiuoroethane, about 30 parts methanol and about 30 parts trichloroethylene.
4. A method for cleaning a solid surface comprising contacting said surface with the composition of claim 1.
5. A method in accordance with claim 4 wherein said composition is in vapor form.
References Cited UNITED STATES PATENTS 11/1966 Hirsch et el. 25267 4/1963 Kvalnes 260652.5
WILLIAM E. SCHULZ, Primary Examiner
US00255972A 1967-10-24 1972-05-23 Azeotropic composition Expired - Lifetime US3833507A (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
US677715D USB677715I5 (en) 1967-10-24
US677715A US3554918A (en) 1967-10-24 1967-10-24 Azeotropic composition
CA027,298A CA955820A (en) 1967-10-24 1968-08-13 Azeotropic composition
US54085A US3671446A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54081A US3671442A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54086A US3671445A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54084A US3671444A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54082A US3671443A (en) 1967-10-24 1970-06-02 Azeotropic composition
US00255972A US3833507A (en) 1967-10-24 1972-05-23 Azeotropic composition

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
US67771567A 1967-10-24 1967-10-24
US5408470A 1970-06-02 1970-06-02
US5408370A 1970-06-02 1970-06-02
US5408570A 1970-06-02 1970-06-02
US5408670A 1970-06-02 1970-06-02
US5408270A 1970-06-02 1970-06-02
US5408170A 1970-06-02 1970-06-02
US00255972A US3833507A (en) 1967-10-24 1972-05-23 Azeotropic composition

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US3833507A true US3833507A (en) 1974-09-03

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US677715D Pending USB677715I5 (en) 1967-10-24
US677715A Expired - Lifetime US3554918A (en) 1967-10-24 1967-10-24 Azeotropic composition
US54084A Expired - Lifetime US3671444A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54085A Expired - Lifetime US3671446A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54081A Expired - Lifetime US3671442A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54082A Expired - Lifetime US3671443A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54086A Expired - Lifetime US3671445A (en) 1967-10-24 1970-06-02 Azeotropic composition
US00255972A Expired - Lifetime US3833507A (en) 1967-10-24 1972-05-23 Azeotropic composition

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US677715D Pending USB677715I5 (en) 1967-10-24
US677715A Expired - Lifetime US3554918A (en) 1967-10-24 1967-10-24 Azeotropic composition
US54084A Expired - Lifetime US3671444A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54085A Expired - Lifetime US3671446A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54081A Expired - Lifetime US3671442A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54082A Expired - Lifetime US3671443A (en) 1967-10-24 1970-06-02 Azeotropic composition
US54086A Expired - Lifetime US3671445A (en) 1967-10-24 1970-06-02 Azeotropic composition

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0105427A1 (en) * 1982-09-27 1984-04-18 Daikin Kogyo Co., Ltd. Use of a composition of 1,1,2,2-tetrachloro-1,2-difluoroethane, 1,1,2-trichloro-1,2,2-trifluoroethane and at least one other organic solvent for cleaning purposes
US4659505A (en) * 1985-02-20 1987-04-21 Daikin Kogyo Co., Ltd. Azeotropic like composition
US4906304A (en) * 1987-01-28 1990-03-06 Kali-Chemie Aktiengesellschaft Difluorotetrachloroethane mixtures and their use in removing waxes

Families Citing this family (12)

* Cited by examiner, † Cited by third party
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
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
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
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
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

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0105427A1 (en) * 1982-09-27 1984-04-18 Daikin Kogyo Co., Ltd. Use of a composition of 1,1,2,2-tetrachloro-1,2-difluoroethane, 1,1,2-trichloro-1,2,2-trifluoroethane and at least one other organic solvent for cleaning purposes
US4517108A (en) * 1982-09-27 1985-05-14 Daikin Kogyo Co., Ltd. Cleaning composition
US4659505A (en) * 1985-02-20 1987-04-21 Daikin Kogyo Co., Ltd. Azeotropic like composition
US4906304A (en) * 1987-01-28 1990-03-06 Kali-Chemie Aktiengesellschaft Difluorotetrachloroethane mixtures and their use in removing waxes

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US3671444A (en) 1972-06-20
US3671443A (en) 1972-06-20
US3671445A (en) 1972-06-20
US3671446A (en) 1972-06-20
US3671442A (en) 1972-06-20
US3554918A (en) 1971-01-12
CA955820A (en) 1974-10-08
USB677715I5 (en)

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