DK151234B - APPLICATION OF A SOLVENT MIXTURE FOR CLEANING OF CONNECTED ELECTRONIC ARTICLES - Google Patents
APPLICATION OF A SOLVENT MIXTURE FOR CLEANING OF CONNECTED ELECTRONIC ARTICLES Download PDFInfo
- Publication number
- DK151234B DK151234B DK239673AA DK239673A DK151234B DK 151234 B DK151234 B DK 151234B DK 239673A A DK239673A A DK 239673AA DK 239673 A DK239673 A DK 239673A DK 151234 B DK151234 B DK 151234B
- Authority
- DK
- Denmark
- Prior art keywords
- alcohol
- methyl
- perchlorethylene
- pentanol
- solvent
- Prior art date
Links
- 239000011877 solvent mixture Substances 0.000 title claims description 8
- 238000004140 cleaning Methods 0.000 title description 5
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 claims description 25
- 229950011008 tetrachloroethylene Drugs 0.000 claims description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 22
- 238000009835 boiling Methods 0.000 claims description 12
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 claims description 10
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 claims description 8
- 239000012535 impurity Substances 0.000 claims description 6
- 229910000679 solder Inorganic materials 0.000 claims description 4
- 238000000746 purification Methods 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 239000002904 solvent Substances 0.000 description 26
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 25
- 239000000203 mixture Substances 0.000 description 18
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 15
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 12
- 230000004907 flux Effects 0.000 description 12
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 10
- 150000001298 alcohols Chemical class 0.000 description 10
- HNVRRHSXBLFLIG-UHFFFAOYSA-N 3-hydroxy-3-methylbut-1-ene Chemical compound CC(C)(O)C=C HNVRRHSXBLFLIG-UHFFFAOYSA-N 0.000 description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 6
- AQIXEPGDORPWBJ-UHFFFAOYSA-N pentan-3-ol Chemical compound CCC(O)CC AQIXEPGDORPWBJ-UHFFFAOYSA-N 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- FRDAATYAJDYRNW-UHFFFAOYSA-N 3-methyl-3-pentanol Chemical compound CCC(C)(O)CC FRDAATYAJDYRNW-UHFFFAOYSA-N 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 4
- 239000002985 plastic film Substances 0.000 description 4
- 229920006255 plastic film Polymers 0.000 description 4
- 238000005476 soldering Methods 0.000 description 4
- BZAZNULYLRVMSW-UHFFFAOYSA-N 2-Methyl-2-buten-3-ol Natural products CC(C)=C(C)O BZAZNULYLRVMSW-UHFFFAOYSA-N 0.000 description 3
- CEBKHWWANWSNTI-UHFFFAOYSA-N 2-methylbut-3-yn-2-ol Chemical compound CC(C)(O)C#C CEBKHWWANWSNTI-UHFFFAOYSA-N 0.000 description 3
- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-methylbutan-1-ol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 description 3
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 description 3
- 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 description 2
- BVOSSZSHBZQJOI-UHFFFAOYSA-N 1-Hexen-3-ol Chemical compound CCCC(O)C=C BVOSSZSHBZQJOI-UHFFFAOYSA-N 0.000 description 2
- TZYRSLHNPKPEFV-UHFFFAOYSA-N 2-ethyl-1-butanol Chemical compound CCC(CC)CO TZYRSLHNPKPEFV-UHFFFAOYSA-N 0.000 description 2
- PFNHSEQQEPMLNI-UHFFFAOYSA-N 2-methyl-1-pentanol Chemical compound CCCC(C)CO PFNHSEQQEPMLNI-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- QXLPXWSKPNOQLE-UHFFFAOYSA-N methylpentynol Chemical compound CCC(C)(O)C#C QXLPXWSKPNOQLE-UHFFFAOYSA-N 0.000 description 2
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 2
- UFLHIIWVXFIJGU-ONEGZZNKSA-N (E)-3-Hexenol Natural products CC\C=C\CCO UFLHIIWVXFIJGU-ONEGZZNKSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- UFLHIIWVXFIJGU-ARJAWSKDSA-N (Z)-hex-3-en-1-ol Chemical compound CC\C=C/CCO UFLHIIWVXFIJGU-ARJAWSKDSA-N 0.000 description 1
- 239000000267 (Z)-hex-3-en-1-ol Substances 0.000 description 1
- 0 *[N+](NO*C*[N+]([O-])I)[O-] Chemical compound *[N+](NO*C*[N+]([O-])I)[O-] 0.000 description 1
- 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
- PUNRPAWKFTXZIW-UHFFFAOYSA-N 3-ethylpent-1-yn-3-ol Chemical compound CCC(O)(CC)C#C PUNRPAWKFTXZIW-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
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000002529 flux (metallurgy) Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- UFLHIIWVXFIJGU-UHFFFAOYSA-N hex-3-en-1-ol Natural products CCC=CCCO UFLHIIWVXFIJGU-UHFFFAOYSA-N 0.000 description 1
- 238000011086 high cleaning Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 238000005507 spraying Methods 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
- 125000006000 trichloroethyl group Chemical group 0.000 description 1
- 239000002023 wood 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
- C11D7/5068—Mixtures of halogenated and non-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
- C23G5/02806—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
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K3/00—Apparatus or processes for manufacturing printed circuits
- H05K3/22—Secondary treatment of printed circuits
- H05K3/26—Cleaning or polishing of the conductive pattern
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00
- H05K2203/07—Treatments involving liquids, e.g. plating, rinsing
- H05K2203/0779—Treatments involving liquids, e.g. plating, rinsing characterised by the specific liquids involved
- H05K2203/0783—Using solvent, e.g. for cleaning; Regulating solvent content of pastes or coatings for adjusting the viscosity
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Metallurgy (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Detergent Compositions (AREA)
- Manufacturing Of Printed Wiring (AREA)
- Cleaning Or Drying Semiconductors (AREA)
Description
i 151234 oin 151234 o
Den foreliggende opfindelse angår anvendelse af en opløsningsmiddelblanding til rensning af loddede elektroniske genstande, såsom trykte kredsløb, for loddepas-ta og andre urenheder. Et trykt kredsløb består af et 5 panel eller et kort, hvorpå der ved hjælp af trykke- eller ætseteknik er påført et elektrisk kredsløb. Derefter monteres forskellige elektroniske komponenter på panelet, hvilke komponenter ved hjælp af lodning forbindes til kredsløbet. Sådanne elektroniske komponenter kan f.eks.The present invention relates to the use of a solvent mixture for the purification of soldered electronic articles, such as printed circuits, for solder fits and other impurities. A printed circuit consists of a 5 panel or a card on which an electrical circuit is applied by means of printing or etching. Then various electronic components are mounted on the panel, which components are soldered to the circuit by means of soldering. Such electronic components can e.g.
10 være transistorer og kondensatorer. Ofte udføres en sådan lodning af kredsløbspanelerne i en loddemaskine. Først ledes panelerne forbi midler, der er bestemt til at påføre flusmiddel til panelerne. Flusmidlet anvendes for at fjerne oxider fra den overflade, der skal loddes. Flus-15 midlet består ofte af træcolophonium. Det påføres fortrinsvis i væskeform, f.eks. ved påsprøjtning.10 being transistors and capacitors. Often, such soldering is done by the circuit panels in a soldering machine. First, the panels are passed by means intended to apply flux to the panels. The flux is used to remove oxides from the surface to be soldered. The flu-15 agent often consists of wood rosin. It is preferably applied in liquid form, e.g. by spraying.
Efter at flusmidlet er påført, bringes panelet med det trykte kredsløb i berøring med et bad af smeltet loddemiddel. Efter at loddeoperationen er tilendebragt, 20 skal panelet normalt renses for at fjerne flusmidlet og andre urenheder. Dette er nødvendigt af forskellige grunde. I drift frembringer elektroniske komponenter varme, som kan forøge deres temperaturer til over 60°C. Flusmidlet kan ved disse forhøjede temperaturer være elektrisk 25 ledende, hvilket kan resultere i uønskede krybestrømme.After the flux is applied, the panel of the printed circuit is brought into contact with a bath of molten solder. After the soldering operation is completed, the panel should normally be cleaned to remove the flux and other impurities. This is necessary for a variety of reasons. In operation, electronic components generate heat that can increase their temperatures to above 60 ° C. The flux may be electrically conductive at these elevated temperatures, which may result in undesirable creep currents.
I de tilfælde, hvor flusmidlet indeholder halogener, kan disse krybestrømme forekomme ved stuetemperatur. En anden grund til, at det er nødvendigt at rense panelet, er, at det normalt er ønskeligt at påføre en plastfilm på pane-30 let med det trykte kredsløb. Selv i små mængder kan tilstedeværelsen af flusmidlet vanskeliggøre eller umuliggøre tilførselen af sådanne plastfilm på panelet med det trykte kredsløb, fordi flusmidlet forhindrer vedhængning af plastfilmen til panelets overflade.In those cases where the flux contains halogens, these creep flows may occur at room temperature. Another reason why it is necessary to clean the panel is that it is usually desirable to apply a plastic film to the panel with the printed circuit. Even in small quantities, the presence of the flux may impede or make it impossible to apply such plastic films to the printed circuit board because the flux prevents adhesion of the plastic film to the panel surface.
35 En anden grund er, at utilstrækkeligt rensede elek troniske komponenter bliver klæbrige og derfor er vanske- 151234 2Another reason is that insufficiently cleaned electronic components become sticky and therefore difficult to remove.
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lige at håndtere, og deres udseende bliver forringet.just to deal with and their appearance deteriorates.
Det er kendt, at paneler med trykte kredsløb kan renses med forskellige opløsningsmidler, såsom en blanding af ethanol og methylchloroform eller en blanding af 5 iso-propanol og trichlortrifluorethan. Anvendelsen af sådanne midler har forårsaget visse ulemper, såsom ringe rensningsaktivitet, en skadelig virkning på de elektroniske komponenter eller risikoen for brand, fordi midlerne er brandfarlige.It is known that printed circuit panels can be purified with various solvents such as a mixture of ethanol and methyl chloroform or a mixture of isopropanol and trichlorotrifluoroethane. The use of such agents has caused certain disadvantages, such as poor cleaning activity, a detrimental effect on the electronic components or the risk of fire because the agents are flammable.
10 Fra· dansk patentansøgning nr. 2072/69 (DK-frem læggelsesskrift nr. 132.588) er det kendt som rensemiddel at anvende blandinger indeholdende tetrachlordifluorethan. Denne forbindelse har et smeltepunkt på +24°C, og selv blandinger med en aliphatisk alkohol har et temmeligt højt 15 smeltepunkt, jfr. tabellen side 5 i den nævnte danske patentansøgning. Disse blandinger må derfor være besværlige at håndtere, da de let størkner ved lavere temperatur. Ved de her omhandlede blandinger foreligger der derimod ingen risiko for størkning.10 From Danish Patent Application No. 2072/69 (Danish Patent Specification No. 132,588) it is known as a cleaning agent to use mixtures containing tetrachlorodifluoroethane. This compound has a melting point of + 24 ° C, and even mixtures with an aliphatic alcohol have a rather high melting point, cf. table 5 in the said Danish patent application. These mixtures must therefore be difficult to handle as they solidify slightly at lower temperature. On the other hand, in the mixtures in question, there is no risk of solidification.
20 En anden fordel ved den foreliggende opfindelse består i, at de anvendte blandinger ikke er brandfarlige, hvorimod de fleste af de i den ovennævnte danske ansøgning nr. 20.72/69 anvendte forbindelser har et flammepunkt, hvilket er yderst uhensigtsmæssigt ud fra et brandsikker-25 hedsmæssigt synspunkt.Another advantage of the present invention is that the mixtures used are non-flammable, whereas most of the compounds used in the aforementioned Danish Application No. 20.72 / 69 have a flash point, which is extremely inappropriate from a fire-proof type. from a standpoint of view.
En yderligere fordel ved de her omhandlede blandinger består i, at de anvendte chlorerede forbindelser er billige og let tilgængelige, medens tetrachlordifluor-ethan ikke er et kommercielt tilgængeligt produkt og er 30 dyrt at fremstille.A further advantage of the present compositions is that the chlorinated compounds used are inexpensive and readily available, while tetrachlorodifluoroethane is not a commercially available product and is expensive to prepare.
Ifølge den foreliggende opfindelse har det vist sig, at der opnås fremragende resultater ved at anvende en opløsningsmiddelblanding, der er ejendommelig ved, at den består af 3-50 vægtprocent af mindst en alkohol med 35 4-6 carbonatomer og 50-97 vægtprocent af mindst ét chlore- ret carbonhydrid af gruppen bestående af perchlorethylen, 151234According to the present invention, it has been found that excellent results are obtained by using a solvent mixture which is characterized in that it consists of 3-50% by weight of at least one alcohol having 35-6 carbon atoms and 50-97% by weight of at least one chlorinated hydrocarbon of the group consisting of perchlorethylene, 151234
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3 trichlorethylen og methylchloroform, til rensning af loddede genstande for loddepasta og andre urenheder.3 trichlorethylene and methyl chloroform, for cleaning soldered solder paste and other impurities.
Alkoholen kan være aliphatisk eller cyclisk. Til dette formål har det vist sig, at pentanol er en særlig 5 anvendelig alkohol, især når den anvendes i kombination med perchlorethylen. Det foretrækkes at anvende et opløsningsmiddel bestående af fra 10 til 20 vægtprocent pentanol og fra 80 til 90 vægtprocent perchlorethylen. Dette opløsningsmiddel er ikke brandfarligt, det har et lavt 10 damptryk, hvilket resulterer i et ringe tab af opløsningsmiddel ved evaporation, og det kan let genvindes ved azeo-trop destillation. Blandt de pentanolisomere foretrækkes anvendelsen af 1-pentanol.The alcohol may be aliphatic or cyclic. For this purpose, it has been found that pentanol is a particularly useful alcohol, especially when used in combination with perchlorethylene. It is preferred to use a solvent consisting of from 10 to 20% by weight pentanol and from 80 to 90% by weight perchlorethylene. This solvent is not flammable, it has a low vapor pressure, resulting in a slight loss of solvent by evaporation, and it can be easily recovered by azeotrop distillation. Among the pentanol isomers, the use of 1-pentanol is preferred.
Anvendelsen af opløsningsmidler indeholdende per-15 chlorethylen foretrækkes, fordi det har vist sig, at de har den mindst skadelige virkning på elektroniske komponenter. Sådanne komponenter er som regel overtrukket med en plastfolie og de er normalt mærket med maling af forskellige farver. Opløsningsmidler indeholdende perchlorethy-20 len kombinerer et lavt angreb på sådanne plastfolier og mærker med en høj rensningseffektivitet på flusmidler og andre urenheder. I opløsningsmidler baseret på perchlorethylen foretrækkes det at anvende alkoholer med et kogepunkt på 115-150°C, hvorved procentindholdet af alkoholen 25 falder inden for det i fig. 1 på den medfølgende tegning viste område. Foretrukne alkoholer, der kan anvendes i kombination med perchlorethylen, er 3-pentanol (kogepunkt 116°C), 1-butanol (kp. 118°C), 2-pentanol (kp. 119°C), 3-methyl-l-pentyn-3-ol (kp. 121°C), 3-methyl-3-pentanol 30 (kp. 122°C), 2-methyl-1-butanol (kp. 128°C), 3-methyl-l--butanol (kp. 130°C), 4-methyl-2-pentanol (kp. 133°C), l-hexen-3-ol (kp. 134°C), blandede isomere af primær amyl-alkohol (kp. 127-139°C), 1-pentanol (kp. 138°C), 3-ethyl--l-pentyn-3-ol (kp. 138°C), cyclopentanol (kp. 141°C), 2-35 -ethyl-l-butanol (kp. 146°C) og 2-methyl-l-pentanol (kp.The use of solvents containing perchlorethylene is preferred because it has been found to have the least detrimental effect on electronic components. Such components are usually coated with a plastic wrap and they are usually marked with paint of different colors. Solvents containing perchlorethylene combine a low attack on such plastic films and labels with a high cleaning efficiency on fluxes and other impurities. In perchlorethylene-based solvents, it is preferred to use alcohols having a boiling point of 115-150 ° C, whereby the percent content of the alcohol 25 falls within that of FIG. 1 in the accompanying drawing. Preferred alcohols that can be used in combination with perchlorethylene are 3-pentanol (bp 116 ° C), 1-butanol (bp 118 ° C), 2-pentanol (bp 119 ° C), 3-methyl-1- pentyn-3-ol (b.p. 121 ° C), 3-methyl-3-pentanol (b.p. 122 ° C), 2-methyl-1-butanol (b.p. 128 ° C), 3-methyl-1- -butanol (b.p. 130 ° C), 4-methyl-2-pentanol (b.p. 133 ° C), 1-hexen-3-ol (b.p. 134 ° C), mixed isomers of primary amyl alcohol (b.p. 127-139 ° C), 1-pentanol (b.p. 138 ° C), 3-ethyl-1-pentyn-3-ol (b.p. 138 ° C), cyclopentanol (b.p. 141 ° C), 2-35 -ethyl-1-butanol (b.p. 146 ° C) and 2-methyl-1-pentanol (b.p.
148°C). Andre anvendelige alkoholer, der kan anvendes i 4 151234148 ° C). Other Applicable Alcohols Usable in 4 151234
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kombination med perchlorethylen, er 2-methyl-3-buten-2--ol (kp. 99°C), 2-butanol (kp. 99°C), 2-methyl-2-butanol (kp. 102°C), 2-methyl-3-butyn-2-ol (kp. 104°C), 2-methyl--1-propanol (kp. 108°C), 2,2-dimethyl-l-propanol (kp.combination with perchlorethylene, is 2-methyl-3-buten-2-ol (bp 99 ° C), 2-butanol (bp 99 ° C), 2-methyl-2-butanol (bp 102 ° C) , 2-methyl-3-butyn-2-ol (b.p. 104 ° C), 2-methyl-1-propanol (b.p. 108 ° C), 2,2-dimethyl-1-propanol (b.p.
5 114°C), 3-hexen-l-ol (kp. 156°C), 1-hexanol (kp. 158°C) og cyclohexanol (kp. 161UC).5 114 ° C), 3-hexen-1-ol (b.p. 156 ° C), 1-hexanol (b.p. 158 ° C) and cyclohexanol (b.p. 161UC).
I opløsningsmidler baseret på trichlorethylen foretrækkes det at anvende alkoholer med et kogepunkt på 90--115°C/ hvorved procentindholdet af alkoholen falder in-10 den for det i fig. 3 på den medfølgende tegning viste område. Foretrukne alkoholer, der kan anvendes i kombination med trichlorethylen, er 2-methyl-3-buten-2-ol (kp. 99°C), 2-butanol (kp. 99°C), 2-methyl-2-butanol (kp. 102°C), 2--methyl-3-butyn-2-ol (kp. 104°C), 2-methyl-1-propanol (kp.In solvents based on trichlorethylene, it is preferred to use alcohols having a boiling point of 90--115 ° C /, whereby the percentage content of the alcohol falls within that of that of FIG. 3 in the accompanying drawing. Preferred alcohols that can be used in combination with trichloroethylene are 2-methyl-3-buten-2-ol (bp 99 ° C), 2-butanol (bp 99 ° C), 2-methyl-2-butanol ( b.p. 102 ° C), 2-methyl-3-butyn-2-ol (b.p. 104 ° C), 2-methyl-1-propanol (b.p.
15 108°C), 2,2-dimethyl-l-propanol (kp. 114°C) og 3-pentanol (kp. 116°C). Andre anvendelige alkoholer, der kan anvendes i kombination med trichlorethylen, er 1-butanol (kp. 118°C), 2-pentanol (kp. 119°C), 3-methyl-l-pentyn-3-ol (kp. 121°C) og 3-methyl-3-pentanol (kp. 122°C).(108 ° C), 2,2-dimethyl-1-propanol (bp 114 ° C) and 3-pentanol (bp 116 ° C). Other useful alcohols that can be used in combination with trichlorethylene are 1-butanol (bp 118 ° C), 2-pentanol (bp 119 ° C), 3-methyl-1-pentyn-3-ol (bp 121 And 3-methyl-3-pentanol (b.p. 122 ° C).
20 I opløsningsmidler baseret på methylchloroform foretrækkes det at anvende alkoholer med et kogepunkt på 82-105°C, hvorved procentindholdet af alkoholen falder inden for det i fig. 2 på den medfølgende tegning viste område. Foretrukne alkoholer, der kan anvendes i kombination 25 med methylchloroform, er 2-methyl-2-propanol (kp. 83°C), 2-methyl-3-buten-2-ol (kp. 99°C), 2-butanol (kp. 99°C), 2- methyl-2-butanol (kp. 102°C) og 2-methyl-3-butyn-2-ol (kp. 104°C). Andre anvendelige alkoholer, der kan anvendes i kombination med methylchloroform, er 2-methyl-1-pro- 30 panol (kp. 108°C), 2,2-dimethyl-l-propanol (kp. 114°C), 3- pentanol (kp. 116°C) og 1-butanol (kp. 118°C).In methyl chloroform-based solvents, it is preferred to use alcohols having a boiling point of 82-105 ° C, whereby the percentage content of the alcohol falls within that of FIG. 2 in the accompanying drawing. Preferred alcohols that can be used in combination with methyl chloroform are 2-methyl-2-propanol (bp 83 ° C), 2-methyl-3-buten-2-ol (bp 99 ° C), 2-butanol (b.p. 99 ° C), 2-methyl-2-butanol (b.p. 102 ° C) and 2-methyl-3-butyn-2-ol (b.p. 104 ° C). Other useful alcohols that can be used in combination with methyl chloroform are 2-methyl-1-propanol (bp 108 ° C), 2,2-dimethyl-1-propanol (bp 114 ° C), 3- pentanol (bp 116 ° C) and 1-butanol (bp 118 ° C).
De følgende eksempler illustrerer nogle særlige anvendelige opløsningsmidler. Dele er vægtdele, medmindre andet er angivet.The following examples illustrate some particularly useful solvents. Parts are parts by weight unless otherwise stated.
35 15123435 151234
OISLAND
5 (1) 13,5% 1-pentanol 86,5% perchlorethylen (2) 10,0% blandede isomere af primær amylalkohol 90,0% perchlorethylen 5 (3) 8,0% 4-methyl-2-pentanol 92,0% perchlorethylen (4) 7,0% 2-ethyl-l-butanol 93,0% perchlorethylen (5) 12,0% 2-butanol 10 88,0% trichlorethylen (6) 7,0% 2-methyl-2-butanol 93,0% trichlorethylen (7) 6,0% 2-methyl-2-propanol 94,0% methylchloroform 15 (8) 5,0% 2-butanol 95,0% methylchloroform.5 (1) 13.5% 1-pentanol 86.5% perchlorethylene (2) 10.0% mixed isomers of primary amyl alcohol 90.0% perchlorethylene 5 (3) 8.0% 4-methyl-2-pentanol 92, 0% perchlorethylene (4) 7.0% 2-ethyl-1-butanol 93.0% perchlorethylene (5) 12.0% 2-butanol 88.0% trichlorethylene (6) 7.0% 2-methyl-2 -butanol 93.0% trichloroethylene (7) 6.0% 2-methyl-2-propanol 94.0% methyl chloroform (8) 5.0% 2-butanol 95.0% methyl chloroform.
Det ifølge den foreliggende opfindelse anvendte opløsningsmiddel kan i nogle tilfælde fremkalde en perfekt rensevirkning på paneler med trykte kredsløb, uden at der 20 behøves nogen mekanisk behandling af panelet. Hvis panelet med trykte kredsløb f.eks. er blevet loddet under anvendelse af flusmidlet "Zeva Flussmittel", type C^p, kan flusmidlet fjernes ved blot at neddyppe panelet ved stuetemperatur i et opløsningsmiddel bestående af 13,5 vægtpro-25 cent 1-pentanol og 86,5 vægtprocent perchlorethylen. IThe solvent used in accordance with the present invention can in some cases produce a perfect cleaning effect on printed circuit panels without requiring any mechanical treatment of the panel. For example, if the printed circuit board. has been soldered using the flux "Zeva Flux Lubricant" type C 2 p, the flux can be removed by simply immersing the panel at room temperature in a solvent consisting of 13.5% by weight 1-pentanol and 86.5% by weight perchlorethylene. IN
andre tilfælde kan det være ønskeligt at forbedre rense-virkningen ved at behandle panelet ved en højere temperatur eller ved samtidig at udsætte panelet for en mekanisk behandling, såsom børstning. En børsteoperation fjerner og-30 så uopløselige urenheder. Det foretrækkes derfor at behandle paneler med trykte kredsløb i en maskine, hvor panelerne udsættes for den samtidige virkning af et opløsningsmiddel og børster. Opløsningsmidlets temperatur er fortrinsvis 20-50°C.in other cases, it may be desirable to improve the cleaning effect by treating the panel at a higher temperature or by simultaneously exposing the panel to a mechanical treatment such as brushing. A brush operation removes and then insoluble impurities. It is therefore preferred to treat printed circuit panels in a machine where the panels are exposed to the simultaneous action of a solvent and brushes. The temperature of the solvent is preferably 20-50 ° C.
35 Opløsningsmidlet ledes fortrinsvis igennem maski nen i modstrøm til panelerne. Det brugte opløsningsmiddel, 6Preferably, the solvent is passed through the machine countercurrent to the panels. The solvent used, 6
OISLAND
151234 der forlader apparatet, genvindes fortrinsvis ved destillation, og det således rensede opløsningsmiddel føres igen ind i maskinen. Den ved destillation tilvejebragte rensning gøres lettere, hvis opløsningsmidlet har en sammen-5 sætning, der er omtrent lig med den azeotrope blanding, der dannes ved destillationsprocessen. En blanding af 1--pentanol og perchlorethylen har f.eks. en azeotrop sammensætning på omtrent 15 vægtprocent 1-pentanol og 85 vægtprocent perchlorethylen og koger ved ca. 119°C. Det skal 10 imidlertid bemærkes, at der på grund af evaporation forekommer et tab af opløsningsmidlet i rensemaskinen. Den bestanddel, der har det laveste kogepunkt, fordamper lettest. I en blanding af 15% 1-pentanol og 85% perchlorethylen er de to bestanddeles evaporationsforhold så forskel-15 ligt fra det azeotrope forhold, at opløsningsmidlet i maskinen vil blive berøvet perchlorethylen. Det er derfor påkrævet, at det nye opløsningsmiddel, der tilføres maskinen for at udligne det tab, der sker ved evaporation, må have en forøget procentdel perchlorethylen. Hvis der f.eks.Preferably, leaving the apparatus is recovered by distillation and the thus-purified solvent is re-introduced into the machine. The purification provided by distillation is facilitated if the solvent has a composition approximately equal to the azeotropic mixture formed by the distillation process. A mixture of 1-pentanol and perchlorethylene has e.g. an azeotropic composition of about 15% by weight of 1-pentanol and 85% by weight of perchlorethylene and boiling at approx. 119 ° C. However, it should be noted that due to evaporation, a loss of the solvent occurs in the purifier. The component with the lowest boiling point evaporates most easily. In a mixture of 15% 1-pentanol and 85% perchlorethylene, the evaporation ratios of the two components are so different from the azeotropic ratio that the solvent in the machine will be deprived of perchlorethylene. Therefore, it is required that the new solvent supplied to the machine to offset the loss caused by evaporation must have an increased percentage of perchlorethylene. For example, if
20 ønskes et opløsningsmiddel bestående af 85% perchlorethylen i maskinen, må det nye opløsningsmiddel afhængig af maskinens konstruktion indeholde f.eks. 90 eller 95% perchlorethylen.If a solvent of 85% perchlorethylene is desired in the machine, the new solvent must, for example, contain e.g. 90 or 95% perchlorethylene.
Efter at have taget tabet på grund af evaporation 25 og den ønskede azeotrope destillation i betragtning, fore trækkes det at give opløsningsmidlet en procentdel alkohol, som afhænger af alkoholens kogepunkt som vist på tegningen, hvor fig. 1 vedrører en blanding af en alkohol og per-30 chlorethylen, fig. 2 en blanding af en alkohol og methylchloro- form, og fig. 3 en blanding af en alkohol og trichlorethy- len.After taking into account the loss due to evaporation 25 and the desired azeotropic distillation, it is preferred to give the solvent a percentage of alcohol which depends on the boiling point of the alcohol as shown in the drawing. 1 relates to a mixture of an alcohol and perchlorethylene; 2 shows a mixture of an alcohol and methyl chloroform; and FIG. 3 a mixture of an alcohol and the trichloroethyl.
35 I hver enkelt figur repræsenterer abscissen alko holens kogepunkt (°C) og ordinaten procentdelen af alko-35 In each figure, the abscissa represents the boiling point of the alcohol (° C) and the ordinate the percentage of alcohol.
OISLAND
7 151234 holen i opløsningsmidlet. Det foretrukne opløsningsmiddel ligger indenfor det område, der er vist i figurerne. Det kan fra fig. 1 f.eks. klart ses, at den foretrukne procentdel af 1-pentanol (kp. 138°C), når den blandes med per-5 chlorethylen,er fra 5 til 20 vægtprocent. Den foretrukne procentdel af cyclopentanol (kp. 141°C) er fra 5 til 18 vægtprocent. Den foretrukne procentdel af 4-methyl-2-pen-tanol (kp. 133°C) er fra 7 til 24 vægtprocent. Den foretrukne procentdel af 2-ethyl-l-butanol (kp. 146°C) er fra 10 5 til 13 vægtprocent. Det er en særlig fordel ved den fore liggende opfindelse, at de fleste af opløsningsmiddelblandingerne ifølge opfindelsen har et højt flammepunkt, således at risikoen for brand formindskes. De alkoholer, som har et højt kogepunkt, frembringer azeotrope blandinger, 15 som intet flammepunkt har. F.eks. har den azeotrope blanding af 1-pentanol og perchlorethylen ikke noget flammepunkt ved en temperatur, der ligger under dens kogepunkt på 119°C.7 The hole in the solvent. The preferred solvent is within the range shown in the figures. It can be seen from FIG. 1 e.g. it is clearly seen that the preferred percentage of 1-pentanol (b.p. 138 ° C) when mixed with per-chloroethylene is from 5 to 20% by weight. The preferred percentage of cyclopentanol (bp 141 ° C) is from 5 to 18% by weight. The preferred percentage of 4-methyl-2-pentanol (bp 133 ° C) is from 7 to 24% by weight. The preferred percentage of 2-ethyl-1-butanol (bp 146 ° C) is from 10 to 13% by weight. It is a particular advantage of the present invention that most of the solvent mixtures of the invention have a high flash point so as to reduce the risk of fire. The alcohols having a high boiling point produce azeotropic mixtures which have no flash point. Eg. For example, the azeotropic mixture of 1-pentanol and perchlorethylene has no flash point at a temperature below its boiling point of 119 ° C.
Claims (4)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE05847/72A SE367847B (en) | 1972-05-03 | 1972-05-03 | |
SE584772 | 1972-05-03 |
Publications (2)
Publication Number | Publication Date |
---|---|
DK151234B true DK151234B (en) | 1987-11-16 |
DK151234C DK151234C (en) | 1988-07-18 |
Family
ID=20267364
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK239673A DK151234C (en) | 1972-05-03 | 1973-05-02 | APPLICATION OF A SOLVENT MIXTURE FOR CLEANING OF CONNECTED ELECTRONIC ARTICLES |
Country Status (10)
Country | Link |
---|---|
JP (1) | JPS5715160B2 (en) |
CH (1) | CH582233A5 (en) |
DE (1) | DE2321880C2 (en) |
DK (1) | DK151234C (en) |
FR (1) | FR2183221B1 (en) |
GB (1) | GB1405692A (en) |
IT (1) | IT1053733B (en) |
NL (1) | NL183559C (en) |
NO (1) | NO146165C (en) |
SE (2) | SE367847B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1442393A (en) * | 1973-02-02 | 1976-07-14 | Ici Ltd | Solvent compositions for cleaning |
US4524011A (en) * | 1982-11-08 | 1985-06-18 | The Dow Chemical Company | Flux removal solvent blend |
JPS6137767U (en) * | 1984-08-10 | 1986-03-08 | 株式会社 田窪工業所 | greenhouse curtain equipment |
JP4743111B2 (en) * | 2006-12-25 | 2011-08-10 | パナソニック電工株式会社 | Recessed lighting fixture |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK132588B (en) * | 1968-04-16 | 1976-01-05 | Ici Ltd | CLEANER |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB472342A (en) * | 1935-05-22 | 1937-09-22 | Ici Ltd | Improvements in or relating to the cleaning and degreasing of materials |
NL109043C (en) * | 1955-02-24 | |||
US3000978A (en) * | 1959-11-12 | 1961-09-19 | Pittsburgh Plate Glass Co | Novel composition |
DE1958875C3 (en) * | 1969-11-24 | 1978-04-13 | Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt | Washing liquid for cleaning the surface of printed circuits |
-
1972
- 1972-05-03 SE SE05847/72A patent/SE367847B/xx unknown
-
1973
- 1973-04-30 DE DE2321880A patent/DE2321880C2/en not_active Expired
- 1973-05-01 GB GB2069273A patent/GB1405692A/en not_active Expired
- 1973-05-02 DK DK239673A patent/DK151234C/en not_active IP Right Cessation
- 1973-05-02 JP JP4860573A patent/JPS5715160B2/ja not_active Expired
- 1973-05-02 NO NO1813/73A patent/NO146165C/en unknown
- 1973-05-02 NL NLAANVRAGE7306119,A patent/NL183559C/en not_active IP Right Cessation
- 1973-05-03 FR FR7315903A patent/FR2183221B1/fr not_active Expired
- 1973-05-03 CH CH630773A patent/CH582233A5/xx not_active IP Right Cessation
- 1973-05-29 IT IT7324772A patent/IT1053733B/en active
- 1973-07-23 SE SE7310240A patent/SE414408B/en unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK132588B (en) * | 1968-04-16 | 1976-01-05 | Ici Ltd | CLEANER |
Also Published As
Publication number | Publication date |
---|---|
CH582233A5 (en) | 1976-11-30 |
NL7306119A (en) | 1973-11-06 |
GB1405692A (en) | 1975-09-10 |
DE2321880C2 (en) | 1983-06-01 |
SE414408B (en) | 1980-07-28 |
IT1053733B (en) | 1981-10-10 |
NL183559B (en) | 1988-06-16 |
NL183559C (en) | 1988-11-16 |
FR2183221B1 (en) | 1977-12-30 |
DK151234C (en) | 1988-07-18 |
FR2183221A1 (en) | 1973-12-14 |
SE367847B (en) | 1974-06-10 |
NO146165C (en) | 1982-08-11 |
NO146165B (en) | 1982-05-03 |
JPS5715160B2 (en) | 1982-03-29 |
DE2321880A1 (en) | 1973-11-15 |
JPS49115983A (en) | 1974-11-06 |
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