[go: up one dir, main page]

US3630926A - Azeotropic composition of 1 1 2 2-tetrachloro - 1 2-difluoroethane and trichloroethylene - Google Patents

Azeotropic composition of 1 1 2 2-tetrachloro - 1 2-difluoroethane and trichloroethylene Download PDF

Info

Publication number
US3630926A
US3630926A US782419A US3630926DA US3630926A US 3630926 A US3630926 A US 3630926A US 782419 A US782419 A US 782419A US 3630926D A US3630926D A US 3630926DA US 3630926 A US3630926 A US 3630926A
Authority
US
United States
Prior art keywords
trichloroethylene
difluoroethane
tetrachloro
azeotropic
composition
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
Application number
US782419A
Inventor
Jan R Haase
John Allan Schofield
Roger A Delano
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Application granted granted Critical
Publication of US3630926A publication Critical patent/US3630926A/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
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C23G5/02806Cleaning 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

  • the disclosure relates to azeotropic mixtures of tetrachlorodifluoroethane and trichloroethylene. It has been discovered that this azeotrope may be used in solvent vapor cleaning and degreasing applications.
  • This invention relates to an azeotropic composition and particularly to the azeotropic mixture of tetrachlorodifluoroethane and trichloroethylene.
  • Chlorofiuoroethane solvents known in the art ordinarily do not have suflicient solvent power to clean printed circuit boards; that is, to effectively remove the rosin flux and other contaminants deposited on the surface of such boards during the application of conductive metal leads thereto.
  • Ultrasonic or vapor degreasing techniques may be used to improve the cleaning action of such solvents.
  • mixtures of solvents have been 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. Additionally, when employing either of these methods the solvent must also be relatively nontoxic and nonflammable for safety reasons.
  • Tetrachlorodifluoroethane is a relatively high boiling halocarbon and for this reason is especially advantageous in vapor degreasing applications. At these higher temperatures the vapor has more of a tendency to dissolve high melting greases, or fluxes as well as oil residues and the like and at a faster rate.
  • the solvent vapors tend to condense on the article until the articles are heated by the vapors from room temperature 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 and wet the surface is especially advantageous.
  • Tetrachlorodifluoroethane also is a better solvent for most types of materials than trichlorotrifluoroethane however, it suffers the disadvantage that it is solidus at room temperature whereas the latter is liquidus. Accordingly tetrachlorodifluoroethane is more diflicult to handle than liquid type cleaning solvents.
  • novel mixtures comprising a two component composition of tetrachlorodifluoroethane (e.g. 1,1,2,2-tetrachloro- 1,2-difluoroethane) as a first component and trichloroethylene as a second component.
  • 1,1,2,2-tetrachloro-l,2-difluoroethane is a preferred tetrachlorodifiuoroethane component
  • the isomer l,1,1,2-tetrachloro- 2,2-difiuoroethane may be substituted as a component therefore in whole or in part and especially in minor amounts or trace amounts.
  • 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 mixtures are 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 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 different proportions 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 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.
  • the present invention relates to the aforementioned azeotropes that boil at atmospheric pressure i about 25, especially i about 15 mm. Hg.
  • An azeotropic composition is obtained by distilling a mixture of 1,1,2,2-tetrachloro-1,Z-difluoroethane and trichloroethylene. The mixture is charged to a laboratory scale distillation flask having an overhead condenser with provision for the removal of the distillate. The mixture is heated to its atmospheric boiling point and distilled at a high reflux.
  • An azeotropic mixture is obtained consisting essentially of the following composition as measured by gas chromatographic analysis, the boiling point of which is measured at substantially 760 millimeter Hg pressure:
  • Trichloroethylene 70. 2 188 be obtained with the following bnary and ternary systems of tetrachlorodifiuoroethane:
  • the azeotropes of the present invention will vary in composition from one fixed pressure as compared to a higher or lower pressure and in each instance the mixture at these various fixed pressures will be a constant boiling mixture and the ratios of the components will not vary.
  • the composition of the azeotrope of this invention will comprise about 29.8 parts by weight I about 10% especially 1 about 5% of l.l.2,2-tetrachloro l.2- difluoroethane and its equivalents, especially those equivalents noted herein and about 70.2 parts by weight about 10% especially about 5% trichloroethylene.
  • the ranges of the azeotropic composition in this manner it is intended for example that the l.l.2.2-tetrachloro-1,2-difluoroethane and its equivalents.
  • azeotrope in an amount comprising about 29.8 parts by weight 1 about 2.98 parts by weight or from about 32.78 parts by weight to about 26.82 parts by weight and the like for the other ranges and components expressed in such a manner.
  • a composition of matter consisting essentially of an azeotrope which at about 760 millimeters of mercury pressure and at about 188 F. consists essentially of about 29.8 percent by weight l,l,2,2-tetrachloro-1,2-difluoroethane and about 70.2 percent by weight trichloroethylene.
  • a method for cleaning a surface by contacting said surface with a composition of matter consisting essentially of an azeotrope which at about 760 millimeters of mercury pressure and at about 188 F. consists essentially of about 29.8 percent by weight 1,1,2,2-tetrachloro-l,Z-difiuoroethane and about 70.2 percent by weight trichloroethylene.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Detergent Compositions (AREA)
  • Manufacturing Of Printed Wiring (AREA)

Abstract

THE DISCLOSURE RELATES TO AZEOTROPIC MIXTURES OF TETRACHLORODIFLUOROETHANE AND TRICHLOROETHYLENE. IT HAS BEEN DISCOVERED THAT THIS AZEOTROPE MAY BE USED IN SOLVENT VAPOR CLEANING AND DEGREASING APPLICATIONS.

Description

United States Patent 3,630,926 AZEOTROPIC COMPOSITION OF 1,1,2,2-TETRA- CHLORO LZ-DIFLUOROETHANE AND TRI- CHLOROETHYLENE Jan R. Haase, Rochester, John Allan Schofield, Irvington, and Roger A. Delano, Dobbs Ferry, N.Y., assignors to Union Carbide Corporation, New York, N.Y. No Drawing. Filed Dec. 9, 1968, Ser. No. 782,419 Int. Cl. C09d 9/00; Clld 7/50; C23g /02 US. Cl. 252171 2 Claims ABSTRACT OF THE DISCLOSURE The disclosure relates to azeotropic mixtures of tetrachlorodifluoroethane and trichloroethylene. It has been discovered that this azeotrope may be used in solvent vapor cleaning and degreasing applications.
This invention relates to an azeotropic composition and particularly to the azeotropic mixture of tetrachlorodifluoroethane and trichloroethylene.
Chlorofiuoroethane solvents known in the art ordinarily do not have suflicient solvent power to clean printed circuit boards; that is, to effectively remove the rosin flux and other contaminants deposited on the surface of such boards during the application of conductive metal leads thereto. Ultrasonic or vapor degreasing techniques may be used to improve the cleaning action of such solvents. Although mixtures of solvents have been 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. Additionally, when employing either of these methods the solvent must also be relatively nontoxic and nonflammable for safety reasons.
Tetrachlorodifluoroethane is a relatively high boiling halocarbon and for this reason is especially advantageous in vapor degreasing applications. At these higher temperatures the vapor has more of a tendency to dissolve high melting greases, or fluxes as well as oil residues and the like and at a faster rate. 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 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 and wet 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 allow for longer periods of cleaning action per unit of time in a continuous vapor degreaser than the lower boiling solvents.
Tetrachlorodifluoroethane also is a better solvent for most types of materials than trichlorotrifluoroethane however, it suffers the disadvantage that it is solidus at room temperature whereas the latter is liquidus. Accordingly tetrachlorodifluoroethane is more diflicult 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 for oils and greases particularly for cleaning printed circuits. A further object is to provide an azeotropic composition which Hce is both relatively nontoxic and noflammable 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 continuous degreasing or ultrasonic means.
The above object of this invention may be accomplished by novel mixtures comprising a two component composition of tetrachlorodifluoroethane (e.g. 1,1,2,2-tetrachloro- 1,2-difluoroethane) as a first component and trichloroethylene as a second component. Although 1,1,2,2-tetrachloro-l,2-difluoroethane is a preferred tetrachlorodifiuoroethane component, the isomer l,1,1,2-tetrachloro- 2,2-difiuoroethane may be substituted as a component therefore in whole or in part and especially in minor amounts or trace amounts. 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 mixtures are 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 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 different proportions 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 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 i about 25, especially i about 15 mm. Hg.
EXAMPLE I An azeotropic composition is obtained by distilling a mixture of 1,1,2,2-tetrachloro-1,Z-difluoroethane and trichloroethylene. The mixture is charged to a laboratory scale distillation flask having an overhead condenser with provision for the removal of the distillate. The mixture is heated to its atmospheric boiling point and distilled at a high reflux. An azeotropic mixture is obtained consisting essentially of the following composition as measured by gas chromatographic analysis, the boiling point of which is measured at substantially 760 millimeter Hg pressure:
Azeotrope Composiboiling tion, perpoint,
cent by F. -760 Ex. Component weight mm. Hg
1 1,1,2,2-tetraehloro-l,2-difluoroethane 29.8 Trichloroethylene 70. 2 188 be obtained with the following bnary and ternary systems of tetrachlorodifiuoroethane:
TABLE I.SYSTEMS WHICH DO NOT FORM AZEOTROPES WITH TETRACHLORODIFLL'OROETIIANE Because of the aforementioned variations in pressure. the azeotropes of the present invention will vary in composition from one fixed pressure as compared to a higher or lower pressure and in each instance the mixture at these various fixed pressures will be a constant boiling mixture and the ratios of the components will not vary. Accordingly, the composition of the azeotrope of this invention will comprise about 29.8 parts by weight I about 10% especially 1 about 5% of l.l.2,2-tetrachloro l.2- difluoroethane and its equivalents, especially those equivalents noted herein and about 70.2 parts by weight about 10% especially about 5% trichloroethylene. By giving the ranges of the azeotropic composition in this manner it is intended for example that the l.l.2.2-tetrachloro-1,2-difluoroethane and its equivalents. especially those equivalents noted herein shall be present in the azeotrope in an amount comprising about 29.8 parts by weight 1 about 2.98 parts by weight or from about 32.78 parts by weight to about 26.82 parts by weight and the like for the other ranges and components expressed in such a manner.
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:
l. A composition of matter consisting essentially of an azeotrope which at about 760 millimeters of mercury pressure and at about 188 F. consists essentially of about 29.8 percent by weight l,l,2,2-tetrachloro-1,2-difluoroethane and about 70.2 percent by weight trichloroethylene.
2. A method for cleaning a surface by contacting said surface with a composition of matter consisting essentially of an azeotrope which at about 760 millimeters of mercury pressure and at about 188 F. consists essentially of about 29.8 percent by weight 1,1,2,2-tetrachloro-l,Z-difiuoroethane and about 70.2 percent by weight trichloroethylene.
References Cited UNITED STATES PATENTS 3,285,858 11/1966 Hirsch et al. 252-171 LEON D. ROSDOL, Primary Examiner W. E. SCHULZ, Assistant Examiner US. Cl. X.R.
l063l l; 25269. 364, Digest 9
US782419A 1968-12-09 1968-12-09 Azeotropic composition of 1 1 2 2-tetrachloro - 1 2-difluoroethane and trichloroethylene Expired - Lifetime US3630926A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US78241968A 1968-12-09 1968-12-09

Publications (1)

Publication Number Publication Date
US3630926A true US3630926A (en) 1971-12-28

Family

ID=25125993

Family Applications (1)

Application Number Title Priority Date Filing Date
US782419A Expired - Lifetime US3630926A (en) 1968-12-09 1968-12-09 Azeotropic composition of 1 1 2 2-tetrachloro - 1 2-difluoroethane and trichloroethylene

Country Status (1)

Country Link
US (1) US3630926A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3951843A (en) * 1973-01-09 1976-04-20 Lfe Corporation Fluorocarbon composition for use in plasma removal of photoresist material from semiconductor devices
US4035258A (en) * 1973-08-27 1977-07-12 Phillips Petroleum Company Azeotropic compositions
US4378303A (en) * 1980-04-14 1983-03-29 Daikin Kogyo Co., Ltd. Azeotropic solvent composition
US4570043A (en) * 1982-07-02 1986-02-11 The Electricity Council Dielectric fluids and apparatus incorporating such fluids

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3951843A (en) * 1973-01-09 1976-04-20 Lfe Corporation Fluorocarbon composition for use in plasma removal of photoresist material from semiconductor devices
US4035258A (en) * 1973-08-27 1977-07-12 Phillips Petroleum Company Azeotropic compositions
US4378303A (en) * 1980-04-14 1983-03-29 Daikin Kogyo Co., Ltd. Azeotropic solvent composition
US4570043A (en) * 1982-07-02 1986-02-11 The Electricity Council Dielectric fluids and apparatus incorporating such fluids

Similar Documents

Publication Publication Date Title
US5246617A (en) Azeotropic compositions of 1,1-dichloro-1-fluoroethane and methanol/ethanol
US4715900A (en) Azeotropic compositions of trichlorotrifluoroethane, dichlorodifluoroethane and methanol/ethanol
US3671443A (en) Azeotropic composition
US5073290A (en) Compositions of 1,1,1,2,2,5,5,5-octafluoro-4-trifluormethypentane and use thereof for cleaning solid surfaces
US4816176A (en) Azeotrope-like compositions of dichlorotrifluoroethane, methanol and nitromethane
US3630926A (en) Azeotropic composition of 1 1 2 2-tetrachloro - 1 2-difluoroethane and trichloroethylene
US3785987A (en) Ternary azeotropic cleaning solution based on tetradichlorodifluoroethane
US3607767A (en) Azeothropic composition of 1,1,2-trifluoroethane,methylene chloride,and cyclopentane
US6010997A (en) Compositions of 1-bromopropane, nitromethane or acetonitrile and an alcohol
US4045366A (en) Azeotrope-like compositions of trichlorotrifluoroethane, nitromethane and acetone
US3737388A (en) Azeotropic composition
US3530073A (en) Azeotropic composition
US4052328A (en) Azeotrope-like compositions of trichlorotrifluoroethane, ethanol, isopropanol and nitromethane
US3539462A (en) Azeotropic composition
US5084199A (en) 1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning
US4812256A (en) Azeotropic compositions of 1,1-difluoro-1,2,2-trichloroethane and methanol, ethanol, isopropanol or n-propanol
EP0389133B1 (en) Azeotropic composition of 2,2-dichloro-1,1,1-trifluoroethane and methanol
US4814100A (en) Azeotropic composition of 1,1-difluoro-2,2-dichloroethane and acetone
JPH04227799A (en) Cleaning composition based on 1,1,1,2,2-pentafluoro- 3,3-dichloropropane and methyl t-butyl ether
US4045365A (en) Azeotrope-like compositions of trichloro-trifluoroethane, acetonitrile and acetone
US5221361A (en) Compositions of 1,1,1,2,2,5,5,5,-octafluoro-4-trifluoromethylpentane and use thereof for cleaning solid surfaces
US4810412A (en) Azeotropic compositions of 1,1-difluoro-2,2-dichloroethane and methanol or ethanol
US3846327A (en) Azeotropic composition
US5176757A (en) 1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning
US5039444A (en) Azeotrope-like compositions of dichloro-trifluoroethane, cyclopentane and optionally nitromethane

Legal Events

Date Code Title Description
AS Assignment

Owner name: MORGAN GUARANTY TRUST COMPANY OF NEW YORK, AND MOR

Free format text: MORTGAGE;ASSIGNORS:UNION CARBIDE CORPORATION, A CORP.,;STP CORPORATION, A CORP. OF DE.,;UNION CARBIDE AGRICULTURAL PRODUCTS CO., INC., A CORP. OF PA.,;AND OTHERS;REEL/FRAME:004547/0001

Effective date: 19860106

AS Assignment

Owner name: UNION CARBIDE CORPORATION,

Free format text: RELEASED BY SECURED PARTY;ASSIGNOR:MORGAN BANK (DELAWARE) AS COLLATERAL AGENT;REEL/FRAME:004665/0131

Effective date: 19860925