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 PDFInfo
- 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
Links
- 239000000203 mixture Substances 0.000 title abstract description 34
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 title abstract description 11
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 title abstract description 11
- 239000002904 solvent Substances 0.000 abstract description 20
- 238000004140 cleaning Methods 0.000 abstract description 10
- 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 7
- 238000005238 degreasing Methods 0.000 abstract description 6
- 238000009835 boiling Methods 0.000 description 11
- 229960002415 trichloroethylene Drugs 0.000 description 9
- 239000013527 degreasing agent Substances 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000012808 vapor phase Substances 0.000 description 3
- 230000009471 action Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-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
- 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 1
- 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 1
- 230000008859 change Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 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 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- 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
- C11D7/504—Azeotropic mixtures containing halogenated solvents all solvents being halogenated hydrocarbons
- C11D7/5059—Mixtures containing (hydro)chlorocarbons
-
- 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 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
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)
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 |
-
1968
- 1968-12-09 US US782419A patent/US3630926A/en not_active Expired - Lifetime
Cited By (4)
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 |