US3729424A - Tertiary azeotropic cleaning solution based on tetrachlorodifluoroethane - Google Patents
Tertiary azeotropic cleaning solution based on tetrachlorodifluoroethane Download PDFInfo
- Publication number
- US3729424A US3729424A US00167012A US3729424DA US3729424A US 3729424 A US3729424 A US 3729424A US 00167012 A US00167012 A US 00167012A US 3729424D A US3729424D A US 3729424DA US 3729424 A US3729424 A US 3729424A
- Authority
- US
- United States
- Prior art keywords
- parts
- tetrachloro
- tetrachlorodifluoroethane
- difluoroethane
- azeotropes
- 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
Links
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
- 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
- C11D7/5086—Mixtures of only oxygen-containing solvents the oxygen-containing solvents being different from alcohols, e.g. mixtures of water and ethers
-
- 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
- This invention relates to binary and ternary azeotropic mixtures of tetrachlorodifluoroethane.
- the binary azeotropes contain tetrachlorodifiuoroethane as one component and either acetic acid, propionic acid, dioxane, monomethyl ether of ethylene glycol, ethyl acetate, isopropyl acetate or n-propyl acetate as the second component.
- the ternary azeotropes contain tetrachlorodifiuoroethane as the first component, 1,2-dichloroethane as the second component and either methanol, ethanol or isopropanol as the third component. It has been discovered that these azeotropes may be used in solvent vapor cleaning and degreasing applications.
- Chlorofiuoroethane solvents known in the art ordinarily do not have sufficient 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 nonfiammable for safety reasons.
- Tetrachlorodifiuoroethane is a relatively high boiling fluorocarbon and for this reason especially advantageous in vapor degreasing applications. At these temperatures the vapor has more of a tendency to dissolve high melting greases, or fiuxed 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.
- Tetrachlorodifiuoroethane also is a better solvent for most types of materials than trichlorotrifiuoroethane however, it suffers the disadvantage that it is solidus at room temperature whereas the latter is liq-uidus. Accordingly tetrachlorodifl'uoroethane is more difficult to handle than liquid type cleaning solvents.
- 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 either acetic acid, propionic acid, dioxane, monomethyl ether of ethylene glycol, ethyl acetate, ispropyl acetate or n-propyl acetate as a second component.
- novel mixtures comprising a three component composition of tetrachlorodifluoroethane (e.g. 1,1,2,2 tetrachloro 1,2 difluoroethane) as a first component, 1,2-dichloroethane as a second component and either methanol, ethanol or isopropanol as a third component.
- 1,1,2,2 tetrachloro 1,2 difluoroethane is a preferred tetrachlorodifluoroethane component
- the isomer 1,1,1,2 tetrachloro 2,2 difluoroethane may be substituted as a component therefore in whole or in part and especially in minor amounts or trace amounts. All of these aforementioned 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 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 aforementioned 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 diiferent 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 or three 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 about i 15 mm. Hg pressure.
- EXAMPLE 1 An azeotropic composition is obtained by distilling a mixture of 1,1,2,2-tetrachloro-l,Z-difluoroethane and acetic acid. The mixture is charged to a laboratory scale distillation flask having an overhead condenser with pro-- vision for the removal of the distillate. The mixture is heated to its atmospheric boiling point and distilled at a high reflux.
- azeotropic mixture consisting 4 essentially of about 93.0 parts 1,l,2,2-tetrachloro-1,2-di- TABLE II.SYSTEMS WHICH DID NOT FORM fluoroethane and about 7.0 parts acetic acid on a weight AZEOTROPES basis, based on refractive index analysis, the boiling point of which is about 194.3 F. :measured at substantially y 760 millimeters Hg pressure.
- Example 1 1, 1,2,2-tetrachloro- 1 ,2-d1fiuoroethane/ acetone
- Example 2-10 1 l ,2,2-tetrachloro 1,2-difluoroethane/ benzene
- the process of Example 1 is repeated using the compo- 1,1,2,2-tetraChI0-Lz-difilloroethane/chlol'ofofm nents noted in Table I and the composition is measured l ac i y i by gas chromatographic analysis and the boiling points of 0 iiig'z i fi i'gfg tg g 'z ,,,-erac oro-,-1uoroe ane epaue each azeotrope measured as m Table L l,1,2,2-tetrachloro-l,Z-difiuoroethane/rnethylene chloride 1, 1,2,2-tetrachloro-1,2-difiuor
- compositions of the azeotrope com- Temary azeotropes ponents as well as their equivalents noted herein will also 8 W 0.28 0 138 3 W as t' Lmicmomet'mne methanoL
- 1,1,2,2- W101 tetrachloro-1,2-difluoroethane in an amount of about 93 l-760I11m- Hg p u parts 1 about 10% shall mean about 83.7 parts to about 102.3 parts on a weight basis and likewise for the other components noted in Table III and the claims as well as A Pnnted clrcult board coated Wlth a rosin flux 15 40 their equivalents, especially those equivalents noted herein.
- a composition of matter consisting essentially of an azeotrope which at about 760 millimeters of mercury pressure and at about 138 F. consists essentially of about 55 percent by weight 1,1,2,2-tetrachloro-1,2-difluoroethane, about 17 percent by weight 1,2-dichloroethane and about 28 percent by weight of methanol.
- 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 138 F. consists essentially of about 55 percent by weight 1,1,2,2-tetrachloro-1,2-
- difluoroethane about 17 percent by weight 1,2-dich1oro- 10 ethane and about 28 percent by weight of methanol.
Landscapes
- 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 TETRACHLORODIFLUOROETHANE, DICHLOROETHANE AND METHANOL HAS SUPERIOR PROPERTIES FOR SOLVENT VAPOR CLEANING AND DEGREASING APPLICATIONS.
Description
United States Patent Oflice 3,729,424 Patented Apr. 24, 1973 TERTIARY AZEOTROPIC CLEANING SOLUTION BASED ON TETRACHLORODIFLUOROETHANE John Allan Schotield, Riverside, Conn., and Roger Albert Delano, Dobbs Ferry, N.Y., assignors to Union Carbide Corporation, New York, N.Y.
No Drawing. Original application Oct. 28, 1968, Ser. No. 771,334, now Patent No. 3,640,884. Divided and this application July 28, 1971, Ser. No. 167,012
Int. Cl. C09d 9/00; Clld 7/52; C23g /02 US. Cl. 252-171 2 Claims ABSTRACT OF THE DISCLOSURE A ternary azeotrope of tetrachlorodifluoroethane, dichloroethane and methanol has superior properties for solvent vapor cleaning and degreasing applications.
This application is a division of our copending US. application Ser. No. 771,334 filed Oct. 28, 1968 and now US. Pat. 3,640,884.
This invention relates to binary and ternary azeotropic mixtures of tetrachlorodifluoroethane. The binary azeotropes contain tetrachlorodifiuoroethane as one component and either acetic acid, propionic acid, dioxane, monomethyl ether of ethylene glycol, ethyl acetate, isopropyl acetate or n-propyl acetate as the second component. The ternary azeotropes contain tetrachlorodifiuoroethane as the first component, 1,2-dichloroethane as the second component and either methanol, ethanol or isopropanol as the third component. It has been discovered that these azeotropes may be used in solvent vapor cleaning and degreasing applications.
Chlorofiuoroethane solvents known in the art ordinarily do not have sufficient 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 nonfiammable for safety reasons.
Tetrachlorodifiuoroethane is a relatively high boiling fluorocarbon and for this reason especially advantageous in vapor degreasing applications. At these temperatures the vapor has more of a tendency to dissolve high melting greases, or fiuxed 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 etfect 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.
Tetrachlorodifiuoroethane also is a better solvent for most types of materials than trichlorotrifiuoroethane however, it suffers the disadvantage that it is solidus at room temperature whereas the latter is liq-uidus. Accordingly tetrachlorodifl'uoroethane is more difficult 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 and particularly for cleaning printed circuits. A further object is to provide an azeotropic composition which is both relatively nontoxic and nonfiammable 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 vapor 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 either acetic acid, propionic acid, dioxane, monomethyl ether of ethylene glycol, ethyl acetate, ispropyl acetate or n-propyl acetate as a second component. The above objects of this invention may also be accomplished by novel mixtures comprising a three component composition of tetrachlorodifluoroethane (e.g. 1,1,2,2 tetrachloro 1,2 difluoroethane) as a first component, 1,2-dichloroethane as a second component and either methanol, ethanol or isopropanol as a third component.
Although 1,1,2,2 tetrachloro 1,2 difluoroethane is a preferred tetrachlorodifluoroethane component, the isomer 1,1,1,2 tetrachloro 2,2 difluoroethane may be substituted as a component therefore in whole or in part and especially in minor amounts or trace amounts. All of these aforementioned 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 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 aforementioned 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 diiferent 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 or three 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 thus Within the skill of the art and is easily determined once it is known that the organic compounds 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 about i 15 mm. Hg pressure.
EXAMPLE 1 An azeotropic composition is obtained by distilling a mixture of 1,1,2,2-tetrachloro-l,Z-difluoroethane and acetic acid. The mixture is charged to a laboratory scale distillation flask having an overhead condenser with pro-- vision 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 4 essentially of about 93.0 parts 1,l,2,2-tetrachloro-1,2-di- TABLE II.SYSTEMS WHICH DID NOT FORM fluoroethane and about 7.0 parts acetic acid on a weight AZEOTROPES basis, based on refractive index analysis, the boiling point of which is about 194.3 F. :measured at substantially y 760 millimeters Hg pressure. Components:
1, 1,2,2-tetrachloro- 1 ,2-d1fiuoroethane/ acetone EXAMPLES 2-10 1 l ,2,2-tetrachloro 1,2-difluoroethane/ benzene The process of Example 1 is repeated using the compo- 1,1,2,2-tetraChI0-Lz-difilloroethane/chlol'ofofm nents noted in Table I and the composition is measured l ac i y i by gas chromatographic analysis and the boiling points of 0 iiig'z i fi i'gfg tg g 'z ,,,-erac oro-,-1uoroe ane epaue each azeotrope measured as m Table L l,1,2,2-tetrachloro-l,Z-difiuoroethane/rnethylene chloride 1, 1,2,2-tetrachloro-1,2-difiuoroethane /perchloroethylene TABLE I 1 1 ,2, Z-tetrachloro- 1 ,2-difluoroethane/ toluene 15 1 l ,2,2-tetrachloro-1,2-difluoroethane/ 1,1,1-trichlorohane E. ease; an 2 T No: Binary azeotropes components p weight) 13. ernary g flfifigf 93-040 194-3 1,l,2,2-tetrachloro-l,2-difluoroethane/methanol/ water 2.- 1,1,2,2-tetrachloro-1,2-difluoroeth- 95- 5 199.3 1,1,2,2-tetrachl0ro-1,Z-difluoroethane/perchloroethylcne/ 3 1 i h i i giiigrifi aainuometnas 0-12 0 197 3 methanol 'a'n'e dioxane. l,1,2,2-tetrachloro-l,Z-difluoroethanelperchloroethylene/ 4..." 1,1,2,2-tetrachl grgJ-l,gggtlllgrgfili 9l.88.2 197 h l 5 5855? y y 1,1,2,2-tetrach1oro-l,Z-difluoroethane/perchloroethylene/ 1,ggfit acgggrzdlfiuoroeth- 7. 2-928 172. 1 lsopropanol 6. 1,l,2,2:tetrachloro-1,2-difiuoroeth- 23.7-76.3 192.0 7 jfgjggtfgggifggfgfg 1910 Because of the fluctuation in ambient pressures as disane n-propyl acetate. cussed previously, the compositions of the azeotrope com- Temary azeotropes ponents as well as their equivalents noted herein will also 8 W 0.28 0 138 3 W as t' Lmicmomet'mne methanoL In the following claims 1t is intended that the compo- 1,1,2,Z-tBtYeGhIOI'OI,Mifluoroefll- 44.0-33-043-0 158-5 nents contained therein as well as those of Table III 10--.. a7.o-3s o-25 o 16M herein and their disclosed and art known equivalents, be
fine 1,2-dich10r0ethaneimpr0- construed in such a manner so that for example 1,1,2,2- W101 tetrachloro-1,2-difluoroethane in an amount of about 93 l-760I11m- Hg p u parts 1 about 10% shall mean about 83.7 parts to about 102.3 parts on a weight basis and likewise for the other components noted in Table III and the claims as well as A Pnnted clrcult board coated Wlth a rosin flux 15 40 their equivalents, especially those equivalents noted herein. clfiallcd in an ultrasonic degfeasl'ng apparatus with the Although the invention has been described by referazeotropic mixtures of this invention and substantially all ence t some f rr d e b diment it is not intended of the rosin flux is removed without any observable detrithat the broad scope of the novel azeotropic compositions TABLE III Components Binary azcotrospes Composition, parts by weight 1,1,2,2-tetrachloro-1,2-difluoroethane About 93 parts :I: about 10% especially i about 5%.
Do Acetic acid About 7 parts :I: about 10% especially :l: about 5%.
About 95 parts :l: about 10% especially :I: about 5%.
Do.. Propionie acid About 5 parts :l: about 10% especially :I: about 6%. Do.. About 88 parts i about 10% especially i about 5%. Do.- About 12 parts :1: about 10% especially i about 5%. Do.. About 91.8 parts i about 10% especially :I: about 5%. Do Monomethyl ether of ethylene glycol About 8.2 parts :i: about 10% especially :l: about 5%. Do About 7.2 parts :I: about 10% especially :1: about 5%. Do Ethyl acetate About 92.8 parts about 10% especially :1: about 5%. D0 About 23.7 parts :I: about 10% especially :l: about 5%. Do Isopropyl acetate... About 76.3 parts :i: about 10% especially :I: about 5%. Do.. About 9.4 parts :l: about 10% especially :I: about 5%. Do n-Propyl acetate About 90.6 parts i about 10% especially :I: about 5%.
Ternary azeotropes Do.. About 55.0 parts :1: about 10% especially :I: about 5%. Do 1,2-dichlomethane... About 17.0 parts i about 10% especially :I: about 5%. Do Me About 28.0 parts i about 10% especially :4: about 5%; Do About 44 parts :I: about 10% especially :1: about 5%. Do 1,2-dichloroethane About 33 parts :1: about 10% especially :1: about 5%. D0 Ei'hannl About 23 parts :I: about 10% especially :1: about 5%. Do About 37 parts :I: abotu 10% especially :I: about 5%. Do 1,2-dichloroethane..- About 38 parts :l: about 10% especially :1: about 5%. Do Isopropanol About 25 parts i about 10% especially :1: about 5%.
mental effect on the board which constitutes the backing of the printed circuit.
The formation of the azeotropes of this invention is unexpected in view of the fact that azeotropes could not be obtained with the following binary and ternary systems of tetrachlorodifluoroethane listed in Table II:
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. A composition of matter consisting essentially of an azeotrope which at about 760 millimeters of mercury pressure and at about 138 F. consists essentially of about 55 percent by weight 1,1,2,2-tetrachloro-1,2-difluoroethane, about 17 percent by weight 1,2-dichloroethane and about 28 percent by weight of methanol.
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 138 F. consists essentially of about 55 percent by weight 1,1,2,2-tetrachloro-1,2-
difluoroethane, about 17 percent by weight 1,2-dich1oro- 10 ethane and about 28 percent by weight of methanol.
References Cited UNITED STATES PATENTS 3,481,883 12/1969 Aoyama et a1. 252171 2,999,816 9/1961 Bennett et a1 252171 3,085,116 4/1963 Kvalnes 252-171 LEON D. ROS-DOL, Primary Examiner W. E. SCHULZ, Assistant Examiner US. Cl. X.R.
252--Digest 9; 260652.5
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US77133468A | 1968-10-28 | 1968-10-28 | |
US16701271A | 1971-07-28 | 1971-07-28 | |
US16703971A | 1971-07-28 | 1971-07-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3729424A true US3729424A (en) | 1973-04-24 |
Family
ID=27389337
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US771334A Expired - Lifetime US3640884A (en) | 1968-10-28 | 1968-10-28 | Azeotropic cleaning solvents based on 1 1 2 2-tetrachloro-1 2-difluoroethane |
US00167039A Expired - Lifetime US3785987A (en) | 1968-10-28 | 1971-07-28 | Ternary azeotropic cleaning solution based on tetradichlorodifluoroethane |
US00167012A Expired - Lifetime US3729424A (en) | 1968-10-28 | 1971-07-28 | Tertiary azeotropic cleaning solution based on tetrachlorodifluoroethane |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US771334A Expired - Lifetime US3640884A (en) | 1968-10-28 | 1968-10-28 | Azeotropic cleaning solvents based on 1 1 2 2-tetrachloro-1 2-difluoroethane |
US00167039A Expired - Lifetime US3785987A (en) | 1968-10-28 | 1971-07-28 | Ternary azeotropic cleaning solution based on tetradichlorodifluoroethane |
Country Status (1)
Country | Link |
---|---|
US (3) | US3640884A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4169807A (en) * | 1978-03-20 | 1979-10-02 | Rca Corporation | Novel solvent drying agent |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3846332A (en) * | 1971-08-02 | 1974-11-05 | Airco Inc | Azeotropes of 1-chloro-2,2,2-trifluoroethyl difluoromethyl ether with acetone, methyl ethylketone and tetrahydrofuran |
US4115914A (en) * | 1976-03-26 | 1978-09-26 | Hughes Aircraft Company | Electrically erasable non-volatile semiconductor memory |
JPS5958099A (en) * | 1982-09-27 | 1984-04-03 | ダイキン工業株式会社 | Detergent composition |
US5246618A (en) * | 1989-01-13 | 1993-09-21 | Kali-Chemie Ag | Cleaning compositions (containing fluorochlorocarbon, C1 to C4 alkanol and ethyl or methyl proprionate) |
DE3911078A1 (en) * | 1989-01-13 | 1990-10-11 | Kali Chemie Ag | CLEANING COMPOSITIONS |
-
1968
- 1968-10-28 US US771334A patent/US3640884A/en not_active Expired - Lifetime
-
1971
- 1971-07-28 US US00167039A patent/US3785987A/en not_active Expired - Lifetime
- 1971-07-28 US US00167012A patent/US3729424A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4169807A (en) * | 1978-03-20 | 1979-10-02 | Rca Corporation | Novel solvent drying agent |
Also Published As
Publication number | Publication date |
---|---|
US3785987A (en) | 1974-01-15 |
US3640884A (en) | 1972-02-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6753304B1 (en) | Compositions comprising perfluorobutyl methyl ether and use of said compositions | |
US5445757A (en) | Compositions comprising pentafluorobutane and use of these compositions | |
US5091104A (en) | Azeotrope-like compositions of tertiary butyl 2,2,2-trifluoroethyl ether and perfluoromethylcyclohexane | |
US3671443A (en) | Azeotropic composition | |
CA1332657C (en) | Azeotropic compositions of 1,1-dichloro-1- fluoroethane and methanol/ethanol | |
KR19980025367A (en) | Azeotropic mixtures of octamethyltrisiloxane with aliphatic or cycloaliphatic alcohols | |
US5073290A (en) | Compositions of 1,1,1,2,2,5,5,5-octafluoro-4-trifluormethypentane and use thereof for cleaning solid surfaces | |
US3729424A (en) | Tertiary azeotropic cleaning solution based on tetrachlorodifluoroethane | |
US3607767A (en) | Azeothropic composition of 1,1,2-trifluoroethane,methylene chloride,and cyclopentane | |
US5824632A (en) | Azeotropes of decamethyltetrasiloxane | |
US3737388A (en) | Azeotropic composition | |
JPH02258732A (en) | Azeotropic or azeotropic-like composition of 1,1,2- trichlorotrifluoroethane and trans-1,2-dichloroethylene with ehtanol,n-propanol,isopropanol or acetone,or with ethanol or acetone and nitromethane | |
US3630926A (en) | Azeotropic composition of 1 1 2 2-tetrachloro - 1 2-difluoroethane and trichloroethylene | |
US3530073A (en) | Azeotropic composition | |
CA1083915A (en) | Azeotrope-like compositions of tri- chlorotrifluoroethane, nitromethane and acetone | |
US3539462A (en) | Azeotropic composition | |
US5413730A (en) | Compositions containing a fluorinated ether and use of these compositions | |
US4812256A (en) | Azeotropic compositions of 1,1-difluoro-1,2,2-trichloroethane and methanol, ethanol, isopropanol or n-propanol | |
US5221361A (en) | Compositions of 1,1,1,2,2,5,5,5,-octafluoro-4-trifluoromethylpentane and use thereof for cleaning solid surfaces | |
US5176757A (en) | 1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning | |
US4810412A (en) | Azeotropic compositions of 1,1-difluoro-2,2-dichloroethane and methanol or ethanol | |
US3607768A (en) | Azeotropic composition | |
US3694368A (en) | Ternary azeotropic compositions | |
US5039444A (en) | Azeotrope-like compositions of dichloro-trifluoroethane, cyclopentane and optionally nitromethane | |
WO1991013846A1 (en) | 1,1,2,2,3,3-hexafluorocyclopentane and use thereof in compositions and processes for cleaning |
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 |