CA2031421A1 - Cleaning composition - Google Patents
Cleaning compositionInfo
- Publication number
- CA2031421A1 CA2031421A1 CA002031421A CA2031421A CA2031421A1 CA 2031421 A1 CA2031421 A1 CA 2031421A1 CA 002031421 A CA002031421 A CA 002031421A CA 2031421 A CA2031421 A CA 2031421A CA 2031421 A1 CA2031421 A1 CA 2031421A1
- Authority
- CA
- Canada
- Prior art keywords
- cleaning composition
- cleaning
- hcf2
- composition according
- pentane
- 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.)
- Abandoned
Links
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
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/261—Alcohols; Phenols
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
-
- 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
- C11D7/5004—Organic solvents
- C11D7/5018—Halogenated solvents
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G5/00—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
- C23G5/02—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
- C23G5/028—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing halogenated hydrocarbons
- C23G5/02803—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 fluorine
-
- 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
- C11D7/22—Organic compounds
- C11D7/24—Hydrocarbons
-
- 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
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/264—Aldehydes; Ketones; Acetals or ketals
-
- 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
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/266—Esters or carbonates
-
- 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
- C11D7/22—Organic compounds
- C11D7/28—Organic compounds containing halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Manufacturing Of Printed Wiring (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE:
The invention provides a cleaning composition containing as an active component an aliphatic fluorohydrocarbon represented by the formula CnFmH2n+2-m wherein 4?n?6 and 6?m?12.
The invention provides a cleaning composition containing as an active component an aliphatic fluorohydrocarbon represented by the formula CnFmH2n+2-m wherein 4?n?6 and 6?m?12.
Description
2~3142~
CLEANING COMPOSITION
The present invention relates to a cleaning composition and more particularly to a cleaning composition which is suitable for removal of fluxes, fats and oils, dust, etc.
deposited on IC components, components of precision instruments or the like.
In the manufacture of IC components, somponents of precision instruments, etc., cleaning has been heretofore conducted usually using an organic solvent to remove the fluxes, dust and the like which deposited on components during assembling. For such cleaning, 1,1,2-trichloro-1,2,2--trifluoroethane (R-113) has been widely used as the organic solvent. R-113 is nonflammable, low in toxicity and excellent in stability. Further, R-113, which has a proper solvency, can selectively dissolve only dirts and is unlikely to corrode metals, plastics, elastomers and the like. Printed boards to be cleaned for removal of fluxes are mostly composite products composed of metals, plastics, elastomers and the like. Also from this viewpoint, R-113 is beneficial.
However, use of R-113 is being restricted because R-113 would be likely to destroy the ozone layer in the stratosphere and may become the cause of cutaneous cancer.
It is an object of the present invention to provide a cleaning composition which is utterly unlikely to destroy ~3~ 421 the ozone layer and which is capable of accomplishing effective cleaning for removal of fluxes, oils and the like.
It is another object of the invention to provide a cleaning composition which has such a suitable solvency that it can selectively dissolve only dirts and it will not corrode metals, plastics, elastomers, etc.
We conducted extensive research to achieve the foregoing objects, and found the following. Specific aliphatic fluorohydrocarbons are (1) entirely free from the possibility of destroying the ozone layer because of the absence of chlorine in the molecule; (2) outstanding in the ability to remove fluxes, fats and oils, dust, etc.; and (3) capable of selectively dissolving only dirts without corroding composite products composed of metals, plastics, elastomers, etc. because of their proper solvency like that of R-113 heretofore used. The present invention has been accomplished based on these novel findings.
~ ccording to the present invention, there is provided a cleaning composition containing as an active component an aliphatic fluorohydrocarbon represented by the formula CI~FmH21~ +2-m wherein ~n<6 and 6<m<12.
The cleaning composition according to the invention contains as an active component an aliphatic fluorohydrocarbon represented by the formula ~ .
2~3~21 CnFmH2,1~2-m wherein 4<n<6 and 6_m<12. Such compound has never been used as a cleaning agent for removing fluxes, fats and oils, etc.
Examples of aliphatic fluorohydrocarbons present in the cleaning composition of the invention are compounds represented by the formulas C4F6H4, C4F8H2, C5F1H5, C5F8H4, C5FgH3/
C5FIoH2/ C6FgHs and C6Fl2H2, respectively. Preferred examples of aliphatic fluorohydrocarbons are 1,1,2,3,4,4-hexafluorobutane (HCF2CFHCFHCF2H), 1, 1, 1, 2,2,3,3,4-octafluorobutanet CF3cF2cF2cH2F) / 1, 1, 2,2,3,3,4-heptafluoropentane(HCF2(CF~)2CFHCH3, 1,1,2,3,3,4,5,5-octafluoropentane(HCF2CFHCF2CFHCF2H), 1, 1,2,2,3,3,4,4,5,-nonafluoropentane (HCF2 (CF2) 3CH2F), 1, 1,1,2,3,3,4,4,5,5,-decafluoropentane ( CF3CF ( CHF2) CF2CF2H), 1, 1, 1, 2,2,3,3,4,4,-nonafluorohexane (CF3 (CF2)3CH2CH3), 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluorohexane (HCF2(CF2)4CF2H), 2-trifluoromethyl-1,1,1,3,4,4,5,5,5-nonafluoropentane ((CF3)2CHCFHCF2CF3), etc.
The above-exemplified alipahtic fluorohydrocarbons can be used singly or at least two of them are usable in mixture.
The amount of the aliphatic fluorohydrocarbon to be contained in the cleaning composition of the invention is not specifically limited, usually about ~0% by weight or more, preferably about 80% by weight or more.
The composition of the invention may contain at least one organic solvent selected from the group consisting of 2~3~21 hydrocarbons, alcohols, esters and ketones in or~er to increase the solvency for dissolving fluxes. The amount of the organic solvent used is not specifically limited, usually about 30% by weight or less, preferably about 0.5 to about 10% by weight, more preferably about 1 to about 8% by weight, based on the whole amount of the cleaning composition of the invention. If the mixture of the aliphatic fluorohydrocarbon and the organic solvent can be an azeotropic composition, it is preferred to use the mixture as the azeotropic composition.
Useful hydrocarbons are not specifically limited.
Preferred hydrocarbons are hexane, heptane, isoheptane, octane, isooctane, methylcyclopentane, cyclohexane, methylcyclohexane, toluene, etc.
Useful alcohols are not specifieally limited.
Preferred alcohols are ehain saturated alcohols having about 1 to about 5 carbon atoms, such as methanol, ethanol, n-propanol, isopropanol, n-butyl alcohol, sec-butyl alcohol, isobutyl alcohol, tert-butyl alcohol, pentyl alcohol, sec-amyl alcohol, 1-ethyl-1-propanol, 2-methyl-1-butanol, isopentyl alcohol, tert-pentyl alcohol, 3-methyl~2-butanol, neopentyl alcohol, 2-ethyl~1-butanol, etc. Among tnem, methanol, ethanol, isopropanol, n-propanol, etc. are desirable.
Useful esters are not specifically limited. Preferred '~3~421 esters are esters of fatty acids having about 1 to about 5 carbon atoms with lower alcohols having about 1 to about 6 carbon atoms, such as methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl acetate, isobutyl acetate, methyl propionate, ethyl propionate, propyl propionate, isopropyl propionate, methyl butyrate, ethyl butyrate, methyl valerate, etc. Among them, methyl acetate, ethyl acetate, propyl acetate, butyl acetate, etc. are preferred.
Useful ketones are not specifically limited. Preferred ketones are those represented by the formula R-CO-R' wherein R and R' each represent a saturated hydrocarbon group having about 1 to about 4 carbon atoms. Examples of such ketones are acetone, 2-butanone, 2-pentanone, 3-pentanone, 4-methyl-2-pentanone, etc. Among them, acetone, 2-butanone, 4-methyl-2-pentanone, etc. are preferred.
The composition of the invention may further contain ingredients heretofore used for this kind of cleaning compositions according to a particular application. Useful ingredients are surfactants and li.ke auxiliary agents for cleaning compositions, stabilizers, hydrogen-containing chlorofluorohydrocarbons which would be less likely to destroy the ozone layer, hydrogen-containing fluorohydrocarbons and other hydrocarbons which are entirely free from the possibility of destroying the ozone layer, and so on. In removal of fluxes, fats and oils, dust, etc.
2~3~21 using the cleaning composition of the invention, a conventional cleaning method can be employed. Such cleaning methods include, for example, manually wiping methods, immersion methods, spraying methods, oscillating methods, ultrasonic cleaning methods, steam cleaning methods, etc.
The cleaning composition of the invention is not prone at all to destroy the ozone layer and is capable of accomplishing effective cleaning for removal of fluxes.
Having a proper solvency like that of R-113 heretofore used, the cleaning composition of the invention can selectively dissolve and remove only dirts (including fluxes, fats and oils, dust, etc.) without corroding composite products composed of metals, plastics, elastomers, etc.
The present invention will be described below in more detail with reference to the following examples.
Example 1 A test for ability to remove fluxes was carried out using the c]eaning compositions Nos. , to 27 of the present invention listed below in Table 1 and containing as an active component 1,1,2,2,3,3,4-heptafluoropentane (7F
pentane), 1,1,2,3,3,4,5,5-octafluoropentane (8F pentane) or 2-trifluoromethyl-1,1,1,3,4,4,5,5,5-nonafluoropentane (6FDH2).
A flux (trade name: Tamura F-Al-4, product of Tamura Seisakusho) was applied on the entire surface of a printed .- :
2~3~2~
board (copper clad laminate). The coated board was preheated at 110C for 20 seconds and soldering was conducted at 250C for 5 seconds. After the soldering, the printed board was immersed in the cleaning composition of the invention, followed by one minute of ultrasonic cleaning. The degree of the removal of the flux was evaluated according to the following criteria. Table 1 shows the results.
A: Flux was removed satisfactorily B: A slight quantity of flux remained unremoved C: A considerable quantity of flux remained unremoved 203~4~1 Table 1 _ _ ¦ No. Composition (wt.~) Result of cleani l 1 7F pentane (100) B
l 11 2 7F pentane (93) Ethanol (7) A
CLEANING COMPOSITION
The present invention relates to a cleaning composition and more particularly to a cleaning composition which is suitable for removal of fluxes, fats and oils, dust, etc.
deposited on IC components, components of precision instruments or the like.
In the manufacture of IC components, somponents of precision instruments, etc., cleaning has been heretofore conducted usually using an organic solvent to remove the fluxes, dust and the like which deposited on components during assembling. For such cleaning, 1,1,2-trichloro-1,2,2--trifluoroethane (R-113) has been widely used as the organic solvent. R-113 is nonflammable, low in toxicity and excellent in stability. Further, R-113, which has a proper solvency, can selectively dissolve only dirts and is unlikely to corrode metals, plastics, elastomers and the like. Printed boards to be cleaned for removal of fluxes are mostly composite products composed of metals, plastics, elastomers and the like. Also from this viewpoint, R-113 is beneficial.
However, use of R-113 is being restricted because R-113 would be likely to destroy the ozone layer in the stratosphere and may become the cause of cutaneous cancer.
It is an object of the present invention to provide a cleaning composition which is utterly unlikely to destroy ~3~ 421 the ozone layer and which is capable of accomplishing effective cleaning for removal of fluxes, oils and the like.
It is another object of the invention to provide a cleaning composition which has such a suitable solvency that it can selectively dissolve only dirts and it will not corrode metals, plastics, elastomers, etc.
We conducted extensive research to achieve the foregoing objects, and found the following. Specific aliphatic fluorohydrocarbons are (1) entirely free from the possibility of destroying the ozone layer because of the absence of chlorine in the molecule; (2) outstanding in the ability to remove fluxes, fats and oils, dust, etc.; and (3) capable of selectively dissolving only dirts without corroding composite products composed of metals, plastics, elastomers, etc. because of their proper solvency like that of R-113 heretofore used. The present invention has been accomplished based on these novel findings.
~ ccording to the present invention, there is provided a cleaning composition containing as an active component an aliphatic fluorohydrocarbon represented by the formula CI~FmH21~ +2-m wherein ~n<6 and 6<m<12.
The cleaning composition according to the invention contains as an active component an aliphatic fluorohydrocarbon represented by the formula ~ .
2~3~21 CnFmH2,1~2-m wherein 4<n<6 and 6_m<12. Such compound has never been used as a cleaning agent for removing fluxes, fats and oils, etc.
Examples of aliphatic fluorohydrocarbons present in the cleaning composition of the invention are compounds represented by the formulas C4F6H4, C4F8H2, C5F1H5, C5F8H4, C5FgH3/
C5FIoH2/ C6FgHs and C6Fl2H2, respectively. Preferred examples of aliphatic fluorohydrocarbons are 1,1,2,3,4,4-hexafluorobutane (HCF2CFHCFHCF2H), 1, 1, 1, 2,2,3,3,4-octafluorobutanet CF3cF2cF2cH2F) / 1, 1, 2,2,3,3,4-heptafluoropentane(HCF2(CF~)2CFHCH3, 1,1,2,3,3,4,5,5-octafluoropentane(HCF2CFHCF2CFHCF2H), 1, 1,2,2,3,3,4,4,5,-nonafluoropentane (HCF2 (CF2) 3CH2F), 1, 1,1,2,3,3,4,4,5,5,-decafluoropentane ( CF3CF ( CHF2) CF2CF2H), 1, 1, 1, 2,2,3,3,4,4,-nonafluorohexane (CF3 (CF2)3CH2CH3), 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluorohexane (HCF2(CF2)4CF2H), 2-trifluoromethyl-1,1,1,3,4,4,5,5,5-nonafluoropentane ((CF3)2CHCFHCF2CF3), etc.
The above-exemplified alipahtic fluorohydrocarbons can be used singly or at least two of them are usable in mixture.
The amount of the aliphatic fluorohydrocarbon to be contained in the cleaning composition of the invention is not specifically limited, usually about ~0% by weight or more, preferably about 80% by weight or more.
The composition of the invention may contain at least one organic solvent selected from the group consisting of 2~3~21 hydrocarbons, alcohols, esters and ketones in or~er to increase the solvency for dissolving fluxes. The amount of the organic solvent used is not specifically limited, usually about 30% by weight or less, preferably about 0.5 to about 10% by weight, more preferably about 1 to about 8% by weight, based on the whole amount of the cleaning composition of the invention. If the mixture of the aliphatic fluorohydrocarbon and the organic solvent can be an azeotropic composition, it is preferred to use the mixture as the azeotropic composition.
Useful hydrocarbons are not specifically limited.
Preferred hydrocarbons are hexane, heptane, isoheptane, octane, isooctane, methylcyclopentane, cyclohexane, methylcyclohexane, toluene, etc.
Useful alcohols are not specifieally limited.
Preferred alcohols are ehain saturated alcohols having about 1 to about 5 carbon atoms, such as methanol, ethanol, n-propanol, isopropanol, n-butyl alcohol, sec-butyl alcohol, isobutyl alcohol, tert-butyl alcohol, pentyl alcohol, sec-amyl alcohol, 1-ethyl-1-propanol, 2-methyl-1-butanol, isopentyl alcohol, tert-pentyl alcohol, 3-methyl~2-butanol, neopentyl alcohol, 2-ethyl~1-butanol, etc. Among tnem, methanol, ethanol, isopropanol, n-propanol, etc. are desirable.
Useful esters are not specifically limited. Preferred '~3~421 esters are esters of fatty acids having about 1 to about 5 carbon atoms with lower alcohols having about 1 to about 6 carbon atoms, such as methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl acetate, isobutyl acetate, methyl propionate, ethyl propionate, propyl propionate, isopropyl propionate, methyl butyrate, ethyl butyrate, methyl valerate, etc. Among them, methyl acetate, ethyl acetate, propyl acetate, butyl acetate, etc. are preferred.
Useful ketones are not specifically limited. Preferred ketones are those represented by the formula R-CO-R' wherein R and R' each represent a saturated hydrocarbon group having about 1 to about 4 carbon atoms. Examples of such ketones are acetone, 2-butanone, 2-pentanone, 3-pentanone, 4-methyl-2-pentanone, etc. Among them, acetone, 2-butanone, 4-methyl-2-pentanone, etc. are preferred.
The composition of the invention may further contain ingredients heretofore used for this kind of cleaning compositions according to a particular application. Useful ingredients are surfactants and li.ke auxiliary agents for cleaning compositions, stabilizers, hydrogen-containing chlorofluorohydrocarbons which would be less likely to destroy the ozone layer, hydrogen-containing fluorohydrocarbons and other hydrocarbons which are entirely free from the possibility of destroying the ozone layer, and so on. In removal of fluxes, fats and oils, dust, etc.
2~3~21 using the cleaning composition of the invention, a conventional cleaning method can be employed. Such cleaning methods include, for example, manually wiping methods, immersion methods, spraying methods, oscillating methods, ultrasonic cleaning methods, steam cleaning methods, etc.
The cleaning composition of the invention is not prone at all to destroy the ozone layer and is capable of accomplishing effective cleaning for removal of fluxes.
Having a proper solvency like that of R-113 heretofore used, the cleaning composition of the invention can selectively dissolve and remove only dirts (including fluxes, fats and oils, dust, etc.) without corroding composite products composed of metals, plastics, elastomers, etc.
The present invention will be described below in more detail with reference to the following examples.
Example 1 A test for ability to remove fluxes was carried out using the c]eaning compositions Nos. , to 27 of the present invention listed below in Table 1 and containing as an active component 1,1,2,2,3,3,4-heptafluoropentane (7F
pentane), 1,1,2,3,3,4,5,5-octafluoropentane (8F pentane) or 2-trifluoromethyl-1,1,1,3,4,4,5,5,5-nonafluoropentane (6FDH2).
A flux (trade name: Tamura F-Al-4, product of Tamura Seisakusho) was applied on the entire surface of a printed .- :
2~3~2~
board (copper clad laminate). The coated board was preheated at 110C for 20 seconds and soldering was conducted at 250C for 5 seconds. After the soldering, the printed board was immersed in the cleaning composition of the invention, followed by one minute of ultrasonic cleaning. The degree of the removal of the flux was evaluated according to the following criteria. Table 1 shows the results.
A: Flux was removed satisfactorily B: A slight quantity of flux remained unremoved C: A considerable quantity of flux remained unremoved 203~4~1 Table 1 _ _ ¦ No. Composition (wt.~) Result of cleani l 1 7F pentane (100) B
l 11 2 7F pentane (93) Ethanol (7) A
3 7F pentane (92) Isopropanol (8) A
4 7F pentane (95) Ethyl acetate (5) A
7F pentane (92) 2-Butanone (8) A
6 7F pentane (95) Methyl acetate (5j A
_ 7 7F pentane (93) Ethanol (5) A
Ethyl acetate (2) 8 7F pentane (94) Ethyl acetate (5) A
2-Butanone (1) _ 9 7F-pentane (93) 2-Butanone (5) A
Ethanol (2) 8F pentane (100) __ B
11 8F pentane (97) Ethanol (3) A
12 8F pentane (95) Isopropanol (5) A
13 8F pentane (96) Ethyl acetate (4) A
14 8F pentane (95) . 2-Butanone (5) A
203~421 Table 1 (continued) No. Composition (wt.%) Result of cleaning 8F pentane (96) Methyl acetate (4) A
16 8F pentane (93) Ethanol (5) A
_ Ethyl acetate (2) 17 8F pentane (94) Ethyl acetate (5) A
2-Butanone (1~
18 8F pentane (93) 2-Butanone (4) A
Ethanol (3) 19 6FDH2 (100) _ B
6FDH2 (80) Ethanol (20) A
21 6FDH2 (75) Isopropanol (25) A
22 6FDH2 (80) Ethyl acetate (20) A
23 6FDH2 (75) 2-Butanone (25) A
24 6FDH2 (80) Methyl acetate (20) A
6FDH2 (80) Ethanol (10) A
Ethyl acetate (10) 26 6FDH2 (75) Ethyl acetate (15) A
2-Butanone (10) _ 27 6FDH2 (80) 2-Butanone (7) A
Ethanol (13) 2~3~2~
~lo--Example 2 In order to check the influence on the plastics materi-als exerted by the cleaning compositions Nos. 1 to 18 used in Example 1, various plastics materials listed below in Table 2 were immersed in each composition at S0C for 1 hour. On withdrawal, the variation (expressed in percent-age) of the weight of each plastics material was measured and the degree of the influence was evaluated according to the following criteria. Table 2 shows the results.
0: Little or no influence was found (Variation of the weight: O to 1%) 1: The plastics material was slightly swelled, but substantially no problem was caused (Variation of the weight: 1 to 5%) 2: The plastics material was swelled and eroded (Variation of weight: 5 to 10%) 203~2~
Table 2 _~
Cleaning composition No.
Resin ___ .____ .___. ____ _._ ____ ____ ____ .___ _ 1 2 3 4 s 5 7 8 9 I _ _ .
¦ABS resin o O O O O O - O O o Polycarbonate O O O O O O O O O
¦Polystyrene O 1 1 1 1 1 1 1 I
¦Polymethacrylate O 1 1 1 1 1 1 1 ~EPOXY resin o o o o o o o o o ¦Phenolic resin O O O O O O O o o ~ _ . ., ..... . .. .. _ ¦Polyphenylene oxide O O O 1 1 1 O 1 l Table 2 (continued) . - Cleaning composition No.
Resin.____ ____ -----T----T----T----T------T----T-----ABS resinO O O ¦ O ¦ o~-¦ O ¦ O ¦ O ¦ O
Polycarbonate O O O ¦ O ¦ O ¦ O ¦ O ¦ O j O
r~ly~ tyr~A~ O 1 _ I I I I I I
Poly- O 1 1 1 1 1 1 1 1 1 1 1 1 1 1 methacrylate ~
l l l l l I
Epoxy resinO O O ¦ O ¦ O ¦ O ¦ O ¦ O ¦ O
~ ----t--------- I
Phenolic resin O O O ¦ O ¦ O ¦ O ¦ O ¦ O ¦ O
_ I .. I
Polyphenylene O O O ¦ 1 ¦ 1 ¦ 1 ¦ O ¦ 1 ¦ 1 oxide _ _ ~
The results shown in Tables 1 and 2 reveal that the composition of the present invention is excellent in ability to effectively remove fluxes and does not erode the plastics materials.
~ 203~2~
~12-Example 3 A flux (trade name: F~AL-4, product of Tamura Seisakusho) was applied on a printed board (10 cm x 10 cm) and the coated board was preheated at 110C. Soldering was conducted at 250C for 5 seconds. A test for ability to remove fluxes was conducted using the cleaning compositions of the invention as listed below in Table 3 by subjecting the printed board treated above to ultrasonic cleaning for 60 seconds and to vapor cleaning for 60 seconds.
After the cleaning, the degree of removal of the flux was evaluated by observing the printed board with the unaided eye and according to the following criteria. On the other hand, the amount of ionic residue was measured using an Omega meter 500 (trade name of a product of KENKO) and utilized for evaluation according to the following criterion. Table 3 shows the results.
Criteria for evaluation of the degree of removal of flux with the unaided eye:
A: The flux was removed satisfactorily B: A slight degree of flux remained unremoved C: A considerable degree of flux remained unremoved Criterion for evaluation by the amount of ionic residue:
Exhibiting satisfactory ability to remove fluxes when the amount of the inonic residue is up to 2 ~gNaCl/cm2 2~ 14~L
Table 3 Ability to remove fluxes Result Ionic (wt%) with residue eye (~gNaCl/cm2) I
¦ HCF2CFHCFHCF2H / C2HsOH 9 3 / 7 A1 . 4 / ( CH3) 2CHOH9 5 / 5 A1 . 5 I
¦ / CH3COOC2H59 7 / 3 A 1.5 /CH3COCzHs 95/5 A1. 8 HCF2(CF2)2CFHCH3/C2HsOH 90/10 A1. 5 / C3H70H 9 2 / 8 A1 . 6 / CH3COOC2H59 5 / 5 A1. 6 /CH3coc2Hs 90/10 A1. 9 HCF2CFHCF2CFHCF2H/C2H50H 90/10 A 1.3 _ / C3H70H 9 5 / 5 A1 . 5 / CH3COOC2Hs9 5 / 5 A1 . 4 _ . .
/ CH3COC2H59 0 /10 A1 . 6 HCF2 ( CF2) 3CH2F / C3H70~9 5 / 5 A1 . 5 CF3CF ( CHF2) C F2CF2H / C3H70H 9 4 / 6 A 1 . 7 /CH3COOC2Hs92/8 A1. 6 CF3(CF2)3CH2CH3/(CH3)2CHOH90/10 A 1.6 HcF2(cF2)4cF2H/c2HsoH 88/12 A1. 5 ( CH3) 2CHOH9 0 /10 A1 . 6 . .... ._ _.
C3H70H 9 2 / 8 A1 . 7 .
CH3COOC2Hs 9 0 /10 A1. 6 _ - ~3142~
-14~
Exam~le 4 A 100 mesh-cylindrical wire net (25~ x 15H mm) on which spindle oil was deposited was immersed in the cleaning composition of the invention heated to 60OC, followed by 60 seconds of ultrasonic cleaning. The wire net was further immersed in a solvent heated to 40 to 60C and subjected to shaking with hands or to ultrasonic cleaning for 60 seconds.
Thereafter, vapor cleaning was conducted for 60 seconds, whereby the cleaning composition was tested for degreasing ability. After the test, the quantity of oil remaining on the wire net was measured by an oil content meter (product of Horiba, Ltd.) and the degree of removal of oils was expressed in cleaning degree (%).
Table 4 below shows the composition of the cleaning compositions used and the cleaning degree.
2~421 Table 4 . - _ Degreasing ability (wt.~) Cleaning degree HCF2CFHCFHCF2H 10 0 9 9 . 6 CF3CF2CF2cH2F 10 0 9 9 . 3 HCF2 (CF2) 2CFHCH3 100 99 . 5 HCF2CFHCF2CFHCF2H 100 99. 6 HCF2 ( CF2 ) 3CH2F 10 0 9 9 . S
CF3CF (CHF2) CF2CF2H 100 99 . 3 CF3 (cF2) 3CH2CH3 100 99 . 2 HCF2 ( CF2) 4CF2H 10 0 9 9 . 2 I
( CF3 ) 2CHCFHCF2CF3 10 0 9 9 . 1 ¦ HCF2CFHCFHCF2H/n-Heptane 70/30 99.9 /Cyclohexane 90/10 99. 7 I . . . .. ___ __ ¦CF3CF2CF2CH2F/n-Heptane 70/30 99.9 ¦ /Cyclohexane 90/10 99.6 ~031421 Table 4 (continued) _ ~
Degreasing abili.ty ¦
(wt.%) Cleaing degree HCF2(CF2)2CFHCH3/n-Heptane 70/30 99.9 /Cyclohexane 90/10 99.7 .
HCF2CFHCF2CFH/n-Heptane 70/30 99.9 /Cyclohexane 90/10 99.7 I
HCF2(CF2)3CH2F/n-Heptane 70/30 99.9 ICyclohexane 90/10 99.6 CF3CF(CHF2)CF2CF2H/n-Heptane 70/30 99.9 . , ~
/Cyclohexane 90/10 99.7 CF3(CF2)3CH2CH3/n-Heptane 70/30 99.8 /Cyclohexane 90/10 99.6 HCF3(CF2)4CF2H/n-Heptane 70/30 99.9 /Cyclohexane 90/10 99.7 (CF3)2CHCFHCF2CF3/n-Heptane 70/30 99 9 /Cyclohexane 90/10 99.6 ~03~2~
As described above, the cleaning compositions of the present invention are excellent in degreasing ability.
7F pentane (92) 2-Butanone (8) A
6 7F pentane (95) Methyl acetate (5j A
_ 7 7F pentane (93) Ethanol (5) A
Ethyl acetate (2) 8 7F pentane (94) Ethyl acetate (5) A
2-Butanone (1) _ 9 7F-pentane (93) 2-Butanone (5) A
Ethanol (2) 8F pentane (100) __ B
11 8F pentane (97) Ethanol (3) A
12 8F pentane (95) Isopropanol (5) A
13 8F pentane (96) Ethyl acetate (4) A
14 8F pentane (95) . 2-Butanone (5) A
203~421 Table 1 (continued) No. Composition (wt.%) Result of cleaning 8F pentane (96) Methyl acetate (4) A
16 8F pentane (93) Ethanol (5) A
_ Ethyl acetate (2) 17 8F pentane (94) Ethyl acetate (5) A
2-Butanone (1~
18 8F pentane (93) 2-Butanone (4) A
Ethanol (3) 19 6FDH2 (100) _ B
6FDH2 (80) Ethanol (20) A
21 6FDH2 (75) Isopropanol (25) A
22 6FDH2 (80) Ethyl acetate (20) A
23 6FDH2 (75) 2-Butanone (25) A
24 6FDH2 (80) Methyl acetate (20) A
6FDH2 (80) Ethanol (10) A
Ethyl acetate (10) 26 6FDH2 (75) Ethyl acetate (15) A
2-Butanone (10) _ 27 6FDH2 (80) 2-Butanone (7) A
Ethanol (13) 2~3~2~
~lo--Example 2 In order to check the influence on the plastics materi-als exerted by the cleaning compositions Nos. 1 to 18 used in Example 1, various plastics materials listed below in Table 2 were immersed in each composition at S0C for 1 hour. On withdrawal, the variation (expressed in percent-age) of the weight of each plastics material was measured and the degree of the influence was evaluated according to the following criteria. Table 2 shows the results.
0: Little or no influence was found (Variation of the weight: O to 1%) 1: The plastics material was slightly swelled, but substantially no problem was caused (Variation of the weight: 1 to 5%) 2: The plastics material was swelled and eroded (Variation of weight: 5 to 10%) 203~2~
Table 2 _~
Cleaning composition No.
Resin ___ .____ .___. ____ _._ ____ ____ ____ .___ _ 1 2 3 4 s 5 7 8 9 I _ _ .
¦ABS resin o O O O O O - O O o Polycarbonate O O O O O O O O O
¦Polystyrene O 1 1 1 1 1 1 1 I
¦Polymethacrylate O 1 1 1 1 1 1 1 ~EPOXY resin o o o o o o o o o ¦Phenolic resin O O O O O O O o o ~ _ . ., ..... . .. .. _ ¦Polyphenylene oxide O O O 1 1 1 O 1 l Table 2 (continued) . - Cleaning composition No.
Resin.____ ____ -----T----T----T----T------T----T-----ABS resinO O O ¦ O ¦ o~-¦ O ¦ O ¦ O ¦ O
Polycarbonate O O O ¦ O ¦ O ¦ O ¦ O ¦ O j O
r~ly~ tyr~A~ O 1 _ I I I I I I
Poly- O 1 1 1 1 1 1 1 1 1 1 1 1 1 1 methacrylate ~
l l l l l I
Epoxy resinO O O ¦ O ¦ O ¦ O ¦ O ¦ O ¦ O
~ ----t--------- I
Phenolic resin O O O ¦ O ¦ O ¦ O ¦ O ¦ O ¦ O
_ I .. I
Polyphenylene O O O ¦ 1 ¦ 1 ¦ 1 ¦ O ¦ 1 ¦ 1 oxide _ _ ~
The results shown in Tables 1 and 2 reveal that the composition of the present invention is excellent in ability to effectively remove fluxes and does not erode the plastics materials.
~ 203~2~
~12-Example 3 A flux (trade name: F~AL-4, product of Tamura Seisakusho) was applied on a printed board (10 cm x 10 cm) and the coated board was preheated at 110C. Soldering was conducted at 250C for 5 seconds. A test for ability to remove fluxes was conducted using the cleaning compositions of the invention as listed below in Table 3 by subjecting the printed board treated above to ultrasonic cleaning for 60 seconds and to vapor cleaning for 60 seconds.
After the cleaning, the degree of removal of the flux was evaluated by observing the printed board with the unaided eye and according to the following criteria. On the other hand, the amount of ionic residue was measured using an Omega meter 500 (trade name of a product of KENKO) and utilized for evaluation according to the following criterion. Table 3 shows the results.
Criteria for evaluation of the degree of removal of flux with the unaided eye:
A: The flux was removed satisfactorily B: A slight degree of flux remained unremoved C: A considerable degree of flux remained unremoved Criterion for evaluation by the amount of ionic residue:
Exhibiting satisfactory ability to remove fluxes when the amount of the inonic residue is up to 2 ~gNaCl/cm2 2~ 14~L
Table 3 Ability to remove fluxes Result Ionic (wt%) with residue eye (~gNaCl/cm2) I
¦ HCF2CFHCFHCF2H / C2HsOH 9 3 / 7 A1 . 4 / ( CH3) 2CHOH9 5 / 5 A1 . 5 I
¦ / CH3COOC2H59 7 / 3 A 1.5 /CH3COCzHs 95/5 A1. 8 HCF2(CF2)2CFHCH3/C2HsOH 90/10 A1. 5 / C3H70H 9 2 / 8 A1 . 6 / CH3COOC2H59 5 / 5 A1. 6 /CH3coc2Hs 90/10 A1. 9 HCF2CFHCF2CFHCF2H/C2H50H 90/10 A 1.3 _ / C3H70H 9 5 / 5 A1 . 5 / CH3COOC2Hs9 5 / 5 A1 . 4 _ . .
/ CH3COC2H59 0 /10 A1 . 6 HCF2 ( CF2) 3CH2F / C3H70~9 5 / 5 A1 . 5 CF3CF ( CHF2) C F2CF2H / C3H70H 9 4 / 6 A 1 . 7 /CH3COOC2Hs92/8 A1. 6 CF3(CF2)3CH2CH3/(CH3)2CHOH90/10 A 1.6 HcF2(cF2)4cF2H/c2HsoH 88/12 A1. 5 ( CH3) 2CHOH9 0 /10 A1 . 6 . .... ._ _.
C3H70H 9 2 / 8 A1 . 7 .
CH3COOC2Hs 9 0 /10 A1. 6 _ - ~3142~
-14~
Exam~le 4 A 100 mesh-cylindrical wire net (25~ x 15H mm) on which spindle oil was deposited was immersed in the cleaning composition of the invention heated to 60OC, followed by 60 seconds of ultrasonic cleaning. The wire net was further immersed in a solvent heated to 40 to 60C and subjected to shaking with hands or to ultrasonic cleaning for 60 seconds.
Thereafter, vapor cleaning was conducted for 60 seconds, whereby the cleaning composition was tested for degreasing ability. After the test, the quantity of oil remaining on the wire net was measured by an oil content meter (product of Horiba, Ltd.) and the degree of removal of oils was expressed in cleaning degree (%).
Table 4 below shows the composition of the cleaning compositions used and the cleaning degree.
2~421 Table 4 . - _ Degreasing ability (wt.~) Cleaning degree HCF2CFHCFHCF2H 10 0 9 9 . 6 CF3CF2CF2cH2F 10 0 9 9 . 3 HCF2 (CF2) 2CFHCH3 100 99 . 5 HCF2CFHCF2CFHCF2H 100 99. 6 HCF2 ( CF2 ) 3CH2F 10 0 9 9 . S
CF3CF (CHF2) CF2CF2H 100 99 . 3 CF3 (cF2) 3CH2CH3 100 99 . 2 HCF2 ( CF2) 4CF2H 10 0 9 9 . 2 I
( CF3 ) 2CHCFHCF2CF3 10 0 9 9 . 1 ¦ HCF2CFHCFHCF2H/n-Heptane 70/30 99.9 /Cyclohexane 90/10 99. 7 I . . . .. ___ __ ¦CF3CF2CF2CH2F/n-Heptane 70/30 99.9 ¦ /Cyclohexane 90/10 99.6 ~031421 Table 4 (continued) _ ~
Degreasing abili.ty ¦
(wt.%) Cleaing degree HCF2(CF2)2CFHCH3/n-Heptane 70/30 99.9 /Cyclohexane 90/10 99.7 .
HCF2CFHCF2CFH/n-Heptane 70/30 99.9 /Cyclohexane 90/10 99.7 I
HCF2(CF2)3CH2F/n-Heptane 70/30 99.9 ICyclohexane 90/10 99.6 CF3CF(CHF2)CF2CF2H/n-Heptane 70/30 99.9 . , ~
/Cyclohexane 90/10 99.7 CF3(CF2)3CH2CH3/n-Heptane 70/30 99.8 /Cyclohexane 90/10 99.6 HCF3(CF2)4CF2H/n-Heptane 70/30 99.9 /Cyclohexane 90/10 99.7 (CF3)2CHCFHCF2CF3/n-Heptane 70/30 99 9 /Cyclohexane 90/10 99.6 ~03~2~
As described above, the cleaning compositions of the present invention are excellent in degreasing ability.
Claims (6)
1. A cleaning composition containing as an active component an aliphatic fluorohydrocarbon represented by the formula CnFmH2n+2-m wherein 4?n?6 and 6?m?12.
2. A cleaning composition according to claim 1 wherein the aliphatic fluorohydrocarbon is at least one compound selected from the group consisting of compounds represented by the formulas C4F6H4, C4F8H2, C5F7H5, C5F8H4, C5F9H3, C5F102, C6F9H5 and C6F12H2, respectively.
3. A cleaning composition according to claim 1 wherein the aliphatic fluorohydrocarbon is at least one compound selected from the group consisting of 1,1,2,3,4,4-hexafluorobutane (HCF2CFHCFHCF2H), 1,1,1,2,2,3,3,4-octafluorobutane (CF3CF2CF2CH2F), 1,1,2,2,3,3,4-heptafluoropentane (HCF2(CF2)2CFHCH3, 1,1,2,3,3,4,5,5-octafluoropentane (HCF2CFHCF2CFHCF2H), 1,1,2,2,3,3,4,4,5,-nonafluoropentane (HCF2(CF2)3CH2F), 1,1,1,2,3,3,4,4,5,5,-decafluoropentane (CF3CF(CHF2)CF2CF2H), 1,1,1,2,2,3,3,4,4,-nonafluorohexane (CF3(CF2)3CH2CH3), 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluorohexane (HCF2(CF2)4CF2H), and 2-trifluoromethyl-1,1,1,3,4,4,5,5,5-nonafluoropentane ((CF3)2CHCFHCF2CF3).
4. A cleaning composition according to claim 1 which contains at least one organic solvent selected from hydrocarbons, alcohols, esters and ketones.
5. A cleaning composition according to claim 1 which contains at least 70% by weight of the aliphatic fluorohydrocarbon.
6. A cleaning composition according to claim 4 which contains about 30% by weight or less of the organic solvent.
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP318644/1989 | 1989-12-07 | ||
| JP31864289 | 1989-12-07 | ||
| JP318642/1989 | 1989-12-07 | ||
| JP31864489 | 1989-12-07 | ||
| JP31864389 | 1989-12-07 | ||
| JP318643/1989 | 1989-12-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2031421A1 true CA2031421A1 (en) | 1991-06-08 |
Family
ID=27339673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002031421A Abandoned CA2031421A1 (en) | 1989-12-07 | 1990-12-04 | Cleaning composition |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP0431458A1 (en) |
| JP (1) | JP2850533B2 (en) |
| KR (1) | KR910012220A (en) |
| AU (1) | AU635362B2 (en) |
| BR (1) | BR9006196A (en) |
| CA (1) | CA2031421A1 (en) |
| CS (1) | CS611190A2 (en) |
| PL (1) | PL288145A1 (en) |
| RU (1) | RU2010847C1 (en) |
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| DE3631561A1 (en) * | 1986-09-17 | 1988-03-31 | Hoechst Ag | SOLUTIONS OF FLUOROPOLYMERS AND THEIR USE |
| US4842764A (en) * | 1988-05-03 | 1989-06-27 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1-dichloro-1-fluoroethane and methanol |
| DE3903336A1 (en) * | 1989-02-04 | 1990-08-09 | Bayer Ag | USING C (ARROW DOWN) 3 (DOWN ARROW) - UP TO C (DOWN ARROW) 5 (DOWN ARROW) -POLYFLUOROUS CANS AS PRESSURE GASES |
-
1990
- 1990-11-26 AU AU66916/90A patent/AU635362B2/en not_active Ceased
- 1990-11-28 EP EP90122748A patent/EP0431458A1/en not_active Withdrawn
- 1990-11-28 JP JP2331976A patent/JP2850533B2/en not_active Expired - Lifetime
- 1990-12-04 CA CA002031421A patent/CA2031421A1/en not_active Abandoned
- 1990-12-06 BR BR909006196A patent/BR9006196A/en not_active Application Discontinuation
- 1990-12-06 RU SU904894031A patent/RU2010847C1/en active
- 1990-12-07 CS CS906111A patent/CS611190A2/en unknown
- 1990-12-07 PL PL28814590A patent/PL288145A1/en unknown
- 1990-12-07 KR KR1019900020128A patent/KR910012220A/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP0431458A1 (en) | 1991-06-12 |
| JPH0428798A (en) | 1992-01-31 |
| RU2010847C1 (en) | 1994-04-15 |
| JP2850533B2 (en) | 1999-01-27 |
| AU635362B2 (en) | 1993-03-18 |
| PL288145A1 (en) | 1991-08-26 |
| BR9006196A (en) | 1991-09-24 |
| AU6691690A (en) | 1991-06-13 |
| CS611190A2 (en) | 1991-09-15 |
| KR910012220A (en) | 1991-08-07 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Dead |