CA2039829A1 - Solvent cleaning of articles - Google Patents
Solvent cleaning of articlesInfo
- Publication number
- CA2039829A1 CA2039829A1 CA002039829A CA2039829A CA2039829A1 CA 2039829 A1 CA2039829 A1 CA 2039829A1 CA 002039829 A CA002039829 A CA 002039829A CA 2039829 A CA2039829 A CA 2039829A CA 2039829 A1 CA2039829 A1 CA 2039829A1
- Authority
- CA
- Canada
- Prior art keywords
- solvent
- cleaning
- composition
- dichloroethane
- dichloro
- 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
- C11D7/50—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
-
- 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
- C23G5/02809—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
- C23G5/02825—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 containing hydrogen
- C23G5/02841—Propanes
- C23G5/02851—C2HCl2F5
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)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
- Manufacturing Of Printed Wiring (AREA)
Abstract
ABSTRACT
"SOLVENT CLEANING OF ARTICLES"
A solvent cleaning composition comprising a mixture, preferably an azeotropic or substantially azeotropic mixture, of dichloropentafluoropropane and 1,1-dichloroethane and its use to clean articles.
"SOLVENT CLEANING OF ARTICLES"
A solvent cleaning composition comprising a mixture, preferably an azeotropic or substantially azeotropic mixture, of dichloropentafluoropropane and 1,1-dichloroethane and its use to clean articles.
Description
203982~
.
. QM 35688 SOLVENT CLEANING OP ARTICLES
This invention relates to solvent cleaning applications in which contaminated articles such as, for example, metals, textiles, glass, plastics, electronic components and printed circuit boards are cleaned using a solvent and/or solvent vapour and more particularly to solvent mixtures useful in solvent cleaning applications and their use.
Solvent cleaning applications wherein contaminated articles are immersed in or washed with halogenated hydrocarbon solvents and/or the vapours thereof are well known and are in common use. Applications involving several stages of immersion, rinsing and drying are common and it is well known to use the solvent at ambient temperature (often accompanied by ultrasonic agitation) or at an elevated temperature up to the boiling point of the solvent. Examples of solvents used in these cleaning processes are 1,1,2-trichloro-1,2,2-trifluoroethane, 1,1,1-trichloroethane, trichloroethylene, perchloroethylene and methylene chloride. These solvents are used alone or in mixtures with cosolvents such as aliphatic alcohols or other low molecular weight, polar additives and depending to some extent upon the articles to be cleaned are often stabilised against degradation induced by light, heat and the presence of metals.
In the known solvent cleaning applications and especially in those applications where the solvent is used at an elevated temperature, there is a tendency for solvent vapour to be lost from the cleaning system into the atmosphere. Purther losses may occur in loading and unloading the solvents into cleaning plant and in recovering used solvent by distillation. Whilst care is usually exercised to minimize losses of solvent into the atmosphere, for instance by improved plant design and 2~39~29 vapour recovery systems, the expense of totally preventing losses is exorbitant and most practical cleaning applications result in some loss of solvent vapour into the atmosphere.
Until recently, the use of the common cleaning solvents has been regarded as an acceptable practice in that the solvents are stable, non-flammable materials of relatively low toxicity believed to be environmentally benign. However recent evidence suggests that some at least of the common solvents may have a long-term deleterious effect on the stratosphere, the so-called ozone layer, so that replacement solvents are seen to be desirable.
According to the invention there is provided a solvent cleaning composition comprising a mixture of at least one isomer of dichloropentafluoropropane and 1,1-dichloroethane.
The dichloropentafluoropropane may be a mixture of isomers but preferably contains at least a major proportion of 1,1-dichloro-2,2,3,3,3-pentafluoro-propane, which is known in the art as "225ca".
1,3-dichloro-1,2,2,3,3-pentafluoropropane which is known in the art as "225cb", is another useful isomer.
1,1-dichloro-2,2,3,3,3-pentafluoropropane and 1,1-dichloroethane form an azeotrope or essentially azeotropic mixture and the azeotrope is a preferred cleaning composition according to the invention, particularly in boiling-solvent cleaning applications.
The azeotrope consists of about 80.5% by weight 1,1-dichloro-2,2,3,3,3-pentafluoropropane and about 19.5% by weight 1,1-dichloroethane and has a boiling point of about 51.4C.
Whilst an azeotrope may be preferred since it maintains an essentially constant composition in use, we 2039~29 .
.
. QM 35688 SOLVENT CLEANING OP ARTICLES
This invention relates to solvent cleaning applications in which contaminated articles such as, for example, metals, textiles, glass, plastics, electronic components and printed circuit boards are cleaned using a solvent and/or solvent vapour and more particularly to solvent mixtures useful in solvent cleaning applications and their use.
Solvent cleaning applications wherein contaminated articles are immersed in or washed with halogenated hydrocarbon solvents and/or the vapours thereof are well known and are in common use. Applications involving several stages of immersion, rinsing and drying are common and it is well known to use the solvent at ambient temperature (often accompanied by ultrasonic agitation) or at an elevated temperature up to the boiling point of the solvent. Examples of solvents used in these cleaning processes are 1,1,2-trichloro-1,2,2-trifluoroethane, 1,1,1-trichloroethane, trichloroethylene, perchloroethylene and methylene chloride. These solvents are used alone or in mixtures with cosolvents such as aliphatic alcohols or other low molecular weight, polar additives and depending to some extent upon the articles to be cleaned are often stabilised against degradation induced by light, heat and the presence of metals.
In the known solvent cleaning applications and especially in those applications where the solvent is used at an elevated temperature, there is a tendency for solvent vapour to be lost from the cleaning system into the atmosphere. Purther losses may occur in loading and unloading the solvents into cleaning plant and in recovering used solvent by distillation. Whilst care is usually exercised to minimize losses of solvent into the atmosphere, for instance by improved plant design and 2~39~29 vapour recovery systems, the expense of totally preventing losses is exorbitant and most practical cleaning applications result in some loss of solvent vapour into the atmosphere.
Until recently, the use of the common cleaning solvents has been regarded as an acceptable practice in that the solvents are stable, non-flammable materials of relatively low toxicity believed to be environmentally benign. However recent evidence suggests that some at least of the common solvents may have a long-term deleterious effect on the stratosphere, the so-called ozone layer, so that replacement solvents are seen to be desirable.
According to the invention there is provided a solvent cleaning composition comprising a mixture of at least one isomer of dichloropentafluoropropane and 1,1-dichloroethane.
The dichloropentafluoropropane may be a mixture of isomers but preferably contains at least a major proportion of 1,1-dichloro-2,2,3,3,3-pentafluoro-propane, which is known in the art as "225ca".
1,3-dichloro-1,2,2,3,3-pentafluoropropane which is known in the art as "225cb", is another useful isomer.
1,1-dichloro-2,2,3,3,3-pentafluoropropane and 1,1-dichloroethane form an azeotrope or essentially azeotropic mixture and the azeotrope is a preferred cleaning composition according to the invention, particularly in boiling-solvent cleaning applications.
The azeotrope consists of about 80.5% by weight 1,1-dichloro-2,2,3,3,3-pentafluoropropane and about 19.5% by weight 1,1-dichloroethane and has a boiling point of about 51.4C.
Whilst an azeotrope may be preferred since it maintains an essentially constant composition in use, we 2039~29 .
have found that some non-azeotropic mixtures, for example that containing about 18% by weight of 1,1-dichloro-2,2,3,3,3-pentafluoropropane, do in fact exhibit acceptable compositional stability in use and may be attractive in affording the possibility of controlling the cleaning power of the cleaning composition.
The amounts of dichloropentafluoropropane and 1,1-dichloroethane in the mixture may vary within wide limits but the mixture should contain sufficient dichloropentafluoropropane to render the mixture non-flammable so that it does not have a flash point.
The mixture should contain at least 15% by weight of the dichloropentafluoropropane. Useful mixtures comprise from 15% to 90% by weight of dichloropentafluoropropane. It is often preferred that the mixture contains from 20X to 80% by weight of the dichloropentafluoropropane. However, we have found that at less than 20X w/w the dichloropentafluoropropane is 20 , an effective diluent for 1,1-dichloroethane.
There are two preferred mixtures for replacing the presently commonly used solvents 1,1,2-trichloro-1,2,2-trifluoroethane and 1,1,1-trichloroethane. One such mixture comprises about 50:50% by weight of the dichloropentafluoropropane and 1,1-dichloroethane; the other comprises about 18:80% bY
weight dichloropentafluoropropane: 1,1-dichloroethane.
In addition to dichloropentafluoropropane and 1,1-dichloroethane, the cleaning composition may contain an aliphatic hydrocarbon and/or a polar compound, for example an aliphatic alcohol, preferably an alcohol containing from 2 to 6 carbon atoms. Methanol, ethanol and propanol, (n-propanol or iso-propanol) are preferred, especially ethanol. The amount of the alcohol may be up to 50% by weight of the composition, although 2~39829 . , amounts below about 10% are preferred. A typlcal ternary mixture contains from about 2% to about 7X by weight of alcohol.
1,1-dichloro-2,2,3,3,3-pentafluoropropane, 1,1-dichloroethane and some at least of the lower alkanols form azeotropes and such ternary azeotropes represent another preferred feature of the invention, particularly in boiling-solvent cleaning applications.
The azeotrope containing methanol boils at about 46.4C and consists of about 76.3% by weight the dichloropentafluoropropane, about 17.7% by weight of 1,1-dichloroethane and about 6% by weight of methanol.
The azeotrope containing ethanol boils at about 51C and consists of about 79% by weight of the dichloropentafluoropropane, about 18X by weight of 1,1-dichloroethane and about 3% by weight of ethanol. On the other hand, a ternary azeotrope containing propanol does not appear to be produced.
As stated, the cleaning composition may contain an aliphatic hydrocarbon, acyclic or cyclic saturated or ethylenically unsaturated hydrocarbons being examples of suitable components. Suitable hydrocarbons, which should be liquids at room temperature, include those having a boiling point in the range 30C to 75C, preferably 40C to 65C. A particularly suitable hydrocarbon for use with 1,1-dichloro-2,2,3,3,3-pentafluoropropane and 1,1,-dichloroethane is cyclopentane, b.p 50C, although the compounds do not appear to form a ternary azeotrope.
As examples of suitable hydrocarbons for incorporation in the solvent cleaning composition according to the present invention may be mentioned inter alia:
2 ~ 2 9 B.Pt. (C) 2-methylbutane (isopentane) 30 2-methyl but-1-ene (amylene) 31 pentane 35-36 2-methyl but-2-ene 35-38 cyclopentane 50 2,2-dimethylbutane (neohexane) 50 4-methyl pent-1-ene 53-54 3-methyl pent-1-ene 54 cis-4-methyl pent-2-ene 57-58 2,3-dimethyl butane 58 2-methyl pentane (isohexane) 61 2-methyl pent-1-ene 62 3-methyl pentane 63 2-methyl-pent-2-ene 67 n-hexane 69 3-methyl pent-2-ene 69 methyl cyclopentane 72 The amount of the hydrocarbon in the solvent cleaning composition may vary within wide limits, for example from 20% to 80% by weight. However, hydrocarbons are generally readily flammable and the amount of the hydrocarbon should preferably be such that the composition remains non-flammable. In particular, the combined amount of hydrocarbon and 1,1-dichloroethane, which is also flammable, should preferably be below that at which the composition is flammable and exhibits a flash point. In addition to the requirement that the liquid composition be non-flammable, any vapours emitted during use of the composition should preferably also be non-fl mmable.
The compositions of the invention may contain one or more stabilisers as are often used in known cleaning compositions, notably nitroalkanes and epoxides.
'-` 2~3~g29 The cleaning compositions of the invention may be used as replacements for the solvents used in any of the known cleaning applications and a process is provided according the invention for cleaning articles which comprises contacting the article(s) with the cleaning composition and/or the vapour thereof. The compositions may be used in cold cleaning applications but will usually be employed at an elevated temperature up to their boiling points.
The invention is illustrated but in no way limited by the following examples.
This Example illustrates the use of an azeotropic mixture according to the present invention for the removal of flux from a printed circuit board.
1,1-dichloro-2,2,3,3,3-pentafluoropropane and 1,1-dichloroethane (80.5X halopropane/19.5X haloethane) was used to remove ionic solder flux residues from circuit boards by the following procedure.
A known weight of solder cream was applied to test boards (5 cm x 7 cm) cut from a copper-coated FR4 board and reflowed in a Micro VPS unit. The solder cream was a 62X tln/38X lead solder available as Multicore PRAB 3.
The solvent was boiled in a beaker fitted with an upper cooling coil through which cold water was circulated to create a boiling liquid phase and a vapour phase. The contaminated test board was dipped into the boiling liquid for 60 seconds and then held in the vapour for 30 seconds.
Residual ionic contamination of the test board, expressed as mg sodium chloride per s~uare centimetre, was determined using a Protonique Contaminometer. The ionic contamination of an unwashed test board was determined and the X removal of ionic contamination by 2~3~2~
the cleaning procedure was calculated. 72.4% of ionic contaminants were removed.
These Examples illustrate the use of ternary azeotropic mixtures according to the present invention for the removal of ionic solder flux from a printed circuit board.
The test procedure described in Example 1 was repeated using the ternary azeotropes described in Table 1.
The results obtained are shown in Table 1.
~39~
~ ''-~ U ____ ~ a u u ~ ~_ ~ ~ ~ ~ ~ .
a a E~
a, ~ ~e a ~ N ~e o~ o ,~
a ~ . a 1~1 ~ ~ Qu ~3~
g This Example illustrates the compatibility of solvent cleaning compositions according to the present invention with plastics materials.
Samples of three plastics materials (A-C) were thoroughly dried by heating in an ov~n at 80C for 1 hour followed by standing in a dessicator for a minimum of 24 hours.
The samples were removed from the dessicator, weighed immediately and then immersed in the boiling solvent for 30 minutes (+ 5 seconds) after which time they were removed and allowed to cool in air for 5 minutes and then weighed. The samples were then placed in a dessicator for 24 hours before being re-weighed.
The results are shown in Table 2.
The plastics materials tested were:-A - Polypropylene copolymer [LYM 123]
B - Nylon [Maranyl A125]
C - epoxy/glass fibre laminate [FR4]
The solvents used in the tests were:-I - An 80:20% by weight mixture of 1,1-dichloro-2,2,3,3,3-pentafluoropropane (DCPFP) and 1,1-dichloroethane (DCE).
II - A 60:40X by weight mixture of DCPFP and DCE.
III - A 20:80X by weight mixture of DCPFP and DCE.
IV - A 79:18:3% by weight mixture of DCPFP, DCE and ethanol.
In a Comparative Test, V - 1,1,2-trichloro-1,2,2-trifluoroethane, was used as solvent.
2~9~29 PLASTIC A ¦ s ¦ C
I l % Weight Change after 30 mins immersion SOLVENT
5 min 24 hr 3 min 24 hr 5 min 24 hr I +1.10 +0.55 -0.01 -0.02 -0.01 0 II +1.98 +0.88 0 +0.01 +0.02 +0.02 III +3.54 +1.35 0 -0.01 +0.62 +0.37 IV +0.97 +0.49 +0.03 0 +0.03 0 V +1.31 +0.57 -0.02 -0.02 0 -0.01 Comparative These Examples illustrate the stability of solvent cleaning compositions according to the present invention against degradation in the presence of aluminium, zinc and mild steel.
Nitromethane (0.3% by weight) was added to the azeotropic mixtures described in Table 3 and the resulting solvents 550 ml) were charged to a reflux apparatus heated on an oil bath.
Weighed test pieces of aluminium, zinc and mild steel were located in the reflux apparatus, partly immersed in the boiling solvent. After approximately 3 days the metal test pieces and the solvent were removed for analysis. The metal pieces were washed with 2~39~9 a small amount of deionised water (which was retained and used later to extract ionic species from the used solvent), rinsed with more water and brushed free of any deposits. They were then rinsed with acetone, dried and re-weighed.
The used solvent was extracted with the metal rinse water (see above) and the extract was analysed for chloride and fluoride ions.
The results were that no change in weight was detected in any of the metal test pieces and no change in halide ion content was detected in the solvent. There was no change in the GC trace for the solvent.
The mild steel test pieces were clean and bright and there was no visual evidence of a tidemark corresponding to the liquid/vapour interface. The aluminium test pieces and the zinc test pieces were also clean and bright although a very slight tidemark was observed on each test piece.
.~
Azeotropic Mixture Example Dichloropenta- 1,1-Dichloro- Ethanol No fluoropropane ethane 225ca 225cb (%)_ (X) (%) (%) 80.5 0 19.5 0 6 0 66~4 29.2 4.4
The amounts of dichloropentafluoropropane and 1,1-dichloroethane in the mixture may vary within wide limits but the mixture should contain sufficient dichloropentafluoropropane to render the mixture non-flammable so that it does not have a flash point.
The mixture should contain at least 15% by weight of the dichloropentafluoropropane. Useful mixtures comprise from 15% to 90% by weight of dichloropentafluoropropane. It is often preferred that the mixture contains from 20X to 80% by weight of the dichloropentafluoropropane. However, we have found that at less than 20X w/w the dichloropentafluoropropane is 20 , an effective diluent for 1,1-dichloroethane.
There are two preferred mixtures for replacing the presently commonly used solvents 1,1,2-trichloro-1,2,2-trifluoroethane and 1,1,1-trichloroethane. One such mixture comprises about 50:50% by weight of the dichloropentafluoropropane and 1,1-dichloroethane; the other comprises about 18:80% bY
weight dichloropentafluoropropane: 1,1-dichloroethane.
In addition to dichloropentafluoropropane and 1,1-dichloroethane, the cleaning composition may contain an aliphatic hydrocarbon and/or a polar compound, for example an aliphatic alcohol, preferably an alcohol containing from 2 to 6 carbon atoms. Methanol, ethanol and propanol, (n-propanol or iso-propanol) are preferred, especially ethanol. The amount of the alcohol may be up to 50% by weight of the composition, although 2~39829 . , amounts below about 10% are preferred. A typlcal ternary mixture contains from about 2% to about 7X by weight of alcohol.
1,1-dichloro-2,2,3,3,3-pentafluoropropane, 1,1-dichloroethane and some at least of the lower alkanols form azeotropes and such ternary azeotropes represent another preferred feature of the invention, particularly in boiling-solvent cleaning applications.
The azeotrope containing methanol boils at about 46.4C and consists of about 76.3% by weight the dichloropentafluoropropane, about 17.7% by weight of 1,1-dichloroethane and about 6% by weight of methanol.
The azeotrope containing ethanol boils at about 51C and consists of about 79% by weight of the dichloropentafluoropropane, about 18X by weight of 1,1-dichloroethane and about 3% by weight of ethanol. On the other hand, a ternary azeotrope containing propanol does not appear to be produced.
As stated, the cleaning composition may contain an aliphatic hydrocarbon, acyclic or cyclic saturated or ethylenically unsaturated hydrocarbons being examples of suitable components. Suitable hydrocarbons, which should be liquids at room temperature, include those having a boiling point in the range 30C to 75C, preferably 40C to 65C. A particularly suitable hydrocarbon for use with 1,1-dichloro-2,2,3,3,3-pentafluoropropane and 1,1,-dichloroethane is cyclopentane, b.p 50C, although the compounds do not appear to form a ternary azeotrope.
As examples of suitable hydrocarbons for incorporation in the solvent cleaning composition according to the present invention may be mentioned inter alia:
2 ~ 2 9 B.Pt. (C) 2-methylbutane (isopentane) 30 2-methyl but-1-ene (amylene) 31 pentane 35-36 2-methyl but-2-ene 35-38 cyclopentane 50 2,2-dimethylbutane (neohexane) 50 4-methyl pent-1-ene 53-54 3-methyl pent-1-ene 54 cis-4-methyl pent-2-ene 57-58 2,3-dimethyl butane 58 2-methyl pentane (isohexane) 61 2-methyl pent-1-ene 62 3-methyl pentane 63 2-methyl-pent-2-ene 67 n-hexane 69 3-methyl pent-2-ene 69 methyl cyclopentane 72 The amount of the hydrocarbon in the solvent cleaning composition may vary within wide limits, for example from 20% to 80% by weight. However, hydrocarbons are generally readily flammable and the amount of the hydrocarbon should preferably be such that the composition remains non-flammable. In particular, the combined amount of hydrocarbon and 1,1-dichloroethane, which is also flammable, should preferably be below that at which the composition is flammable and exhibits a flash point. In addition to the requirement that the liquid composition be non-flammable, any vapours emitted during use of the composition should preferably also be non-fl mmable.
The compositions of the invention may contain one or more stabilisers as are often used in known cleaning compositions, notably nitroalkanes and epoxides.
'-` 2~3~g29 The cleaning compositions of the invention may be used as replacements for the solvents used in any of the known cleaning applications and a process is provided according the invention for cleaning articles which comprises contacting the article(s) with the cleaning composition and/or the vapour thereof. The compositions may be used in cold cleaning applications but will usually be employed at an elevated temperature up to their boiling points.
The invention is illustrated but in no way limited by the following examples.
This Example illustrates the use of an azeotropic mixture according to the present invention for the removal of flux from a printed circuit board.
1,1-dichloro-2,2,3,3,3-pentafluoropropane and 1,1-dichloroethane (80.5X halopropane/19.5X haloethane) was used to remove ionic solder flux residues from circuit boards by the following procedure.
A known weight of solder cream was applied to test boards (5 cm x 7 cm) cut from a copper-coated FR4 board and reflowed in a Micro VPS unit. The solder cream was a 62X tln/38X lead solder available as Multicore PRAB 3.
The solvent was boiled in a beaker fitted with an upper cooling coil through which cold water was circulated to create a boiling liquid phase and a vapour phase. The contaminated test board was dipped into the boiling liquid for 60 seconds and then held in the vapour for 30 seconds.
Residual ionic contamination of the test board, expressed as mg sodium chloride per s~uare centimetre, was determined using a Protonique Contaminometer. The ionic contamination of an unwashed test board was determined and the X removal of ionic contamination by 2~3~2~
the cleaning procedure was calculated. 72.4% of ionic contaminants were removed.
These Examples illustrate the use of ternary azeotropic mixtures according to the present invention for the removal of ionic solder flux from a printed circuit board.
The test procedure described in Example 1 was repeated using the ternary azeotropes described in Table 1.
The results obtained are shown in Table 1.
~39~
~ ''-~ U ____ ~ a u u ~ ~_ ~ ~ ~ ~ ~ .
a a E~
a, ~ ~e a ~ N ~e o~ o ,~
a ~ . a 1~1 ~ ~ Qu ~3~
g This Example illustrates the compatibility of solvent cleaning compositions according to the present invention with plastics materials.
Samples of three plastics materials (A-C) were thoroughly dried by heating in an ov~n at 80C for 1 hour followed by standing in a dessicator for a minimum of 24 hours.
The samples were removed from the dessicator, weighed immediately and then immersed in the boiling solvent for 30 minutes (+ 5 seconds) after which time they were removed and allowed to cool in air for 5 minutes and then weighed. The samples were then placed in a dessicator for 24 hours before being re-weighed.
The results are shown in Table 2.
The plastics materials tested were:-A - Polypropylene copolymer [LYM 123]
B - Nylon [Maranyl A125]
C - epoxy/glass fibre laminate [FR4]
The solvents used in the tests were:-I - An 80:20% by weight mixture of 1,1-dichloro-2,2,3,3,3-pentafluoropropane (DCPFP) and 1,1-dichloroethane (DCE).
II - A 60:40X by weight mixture of DCPFP and DCE.
III - A 20:80X by weight mixture of DCPFP and DCE.
IV - A 79:18:3% by weight mixture of DCPFP, DCE and ethanol.
In a Comparative Test, V - 1,1,2-trichloro-1,2,2-trifluoroethane, was used as solvent.
2~9~29 PLASTIC A ¦ s ¦ C
I l % Weight Change after 30 mins immersion SOLVENT
5 min 24 hr 3 min 24 hr 5 min 24 hr I +1.10 +0.55 -0.01 -0.02 -0.01 0 II +1.98 +0.88 0 +0.01 +0.02 +0.02 III +3.54 +1.35 0 -0.01 +0.62 +0.37 IV +0.97 +0.49 +0.03 0 +0.03 0 V +1.31 +0.57 -0.02 -0.02 0 -0.01 Comparative These Examples illustrate the stability of solvent cleaning compositions according to the present invention against degradation in the presence of aluminium, zinc and mild steel.
Nitromethane (0.3% by weight) was added to the azeotropic mixtures described in Table 3 and the resulting solvents 550 ml) were charged to a reflux apparatus heated on an oil bath.
Weighed test pieces of aluminium, zinc and mild steel were located in the reflux apparatus, partly immersed in the boiling solvent. After approximately 3 days the metal test pieces and the solvent were removed for analysis. The metal pieces were washed with 2~39~9 a small amount of deionised water (which was retained and used later to extract ionic species from the used solvent), rinsed with more water and brushed free of any deposits. They were then rinsed with acetone, dried and re-weighed.
The used solvent was extracted with the metal rinse water (see above) and the extract was analysed for chloride and fluoride ions.
The results were that no change in weight was detected in any of the metal test pieces and no change in halide ion content was detected in the solvent. There was no change in the GC trace for the solvent.
The mild steel test pieces were clean and bright and there was no visual evidence of a tidemark corresponding to the liquid/vapour interface. The aluminium test pieces and the zinc test pieces were also clean and bright although a very slight tidemark was observed on each test piece.
.~
Azeotropic Mixture Example Dichloropenta- 1,1-Dichloro- Ethanol No fluoropropane ethane 225ca 225cb (%)_ (X) (%) (%) 80.5 0 19.5 0 6 0 66~4 29.2 4.4
Claims (13)
1. A solvent cleaning composition comprising a mixture of at least one isomer of dichloropentafluoro-propane and 1,1-dichloroethane.
2. A solvent cleaning composition as claimed in Claim 1 wherein a major proportion of the dichloropenta-fluoropropane is 1,1-dichloro-2,2,3,3,3-pentafluoro-propane.
3. A solvent cleaning composition as claimed in Claim 2 comprising up to about 20% w/w 1,1-dichloro-ethane.
4. A solvent composition as claimed in Claim 1 containing from 15-90% w/w of dichloropentafluoro-propane.
5. A solvent composition as claimed in Claim 2 wherein the 1,1-dichloro-2,2,3,3,3-pentafluoropropane and 1,1-dichloroethane are in the form of an azeotropic or substantially azeotropic mixture.
6. A solvent composition as claimed in Claim 1 further comprising an aliphatic hydrocarbon or polar organic compound or both.
7. A solvent composition as claimed in Claim 6 wherein the polar organic compound is an alcohol containing 2 to 6 carbon atoms.
8. A solvent composition as claimed in Claim 7 containing up to about 10% w/w of the alcohol.
9. A solvent composition as claimed in Claim 7 wherein 1,1-dichloro-2,2,3,3,3-pentafluoroethane, 1,1-dichloroethane and the alcohol form an azeotrope.
10. A solvent composition as claimed in Claim 9 wherein the alcohol is methanol or ethanol.
11. A solvent composition as claimed in Claim 6 comprising 1,1-dichloro-2,2,3,3,3-pentafluoropropane, 1,1-dichloroethane and cyclopentane.
12. A process for cleaning articles which comprises contacting the article(s) with the solvent composition claimed in Claim 1, or the vapour thereof, or both.
13. A process for cleaning articles as claimed in Claim 12 caried out at elevated temperature.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9007578.9 | 1990-04-04 | ||
| GB909007578A GB9007578D0 (en) | 1990-04-04 | 1990-04-04 | Solvent cleaning of articles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2039829A1 true CA2039829A1 (en) | 1991-10-05 |
Family
ID=10673848
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002039829A Abandoned CA2039829A1 (en) | 1990-04-04 | 1991-04-04 | Solvent cleaning of articles |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0450856A3 (en) |
| JP (1) | JPH05295394A (en) |
| KR (1) | KR910018531A (en) |
| AU (1) | AU7391491A (en) |
| CA (1) | CA2039829A1 (en) |
| GB (1) | GB9007578D0 (en) |
| IE (1) | IE911026A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IE902926A1 (en) * | 1989-10-06 | 1991-04-10 | Allied Signal Inc | Azeotrope-like compositions of dichloropentafluoropropane¹and 1,2-dichloroethylene |
| IE66347B1 (en) * | 1989-10-06 | 1995-12-27 | Allied Signal Inc | Azeotrope-like compositions of dichloropentafluoropropane and a hydrocarbon containing sex carbon atoms |
| UA40695U (en) * | 2008-10-23 | 2009-04-27 | Виктор Владимирович МУЖИЧУК | Perforated profile for quick-assembled constructions |
| JP6647269B2 (en) * | 2017-12-21 | 2020-02-14 | 株式会社Ｅｎｅｏｓサンエナジー | Solvent composition |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3634273A (en) * | 1968-01-10 | 1972-01-11 | Armour Ind Chem Co | Thickened chlorinated solvent compositions and method |
| WO1989012674A1 (en) * | 1988-06-22 | 1989-12-28 | Asahi Glass Company Ltd. | Halogenated hydrocarbon solvents and use thereof |
-
1990
- 1990-04-04 GB GB909007578A patent/GB9007578D0/en active Pending
-
1991
- 1991-03-27 EP EP19910302702 patent/EP0450856A3/en not_active Withdrawn
- 1991-03-27 IE IE102691A patent/IE911026A1/en unknown
- 1991-03-28 AU AU73914/91A patent/AU7391491A/en not_active Abandoned
- 1991-04-04 JP JP3071817A patent/JPH05295394A/en active Pending
- 1991-04-04 KR KR1019910005445A patent/KR910018531A/en not_active Application Discontinuation
- 1991-04-04 CA CA002039829A patent/CA2039829A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| KR910018531A (en) | 1991-11-30 |
| IE911026A1 (en) | 1991-10-09 |
| EP0450856A2 (en) | 1991-10-09 |
| JPH05295394A (en) | 1993-11-09 |
| GB9007578D0 (en) | 1990-05-30 |
| AU7391491A (en) | 1991-10-10 |
| EP0450856A3 (en) | 1991-11-21 |
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