EP0456551A1 - 1,1,1,2,2-Pentafluor-3,3-Dichlor-Propan und Methyl Ter-Butyl-Aether enthaltende Reinigungsmittelzusammensetzung - Google Patents
1,1,1,2,2-Pentafluor-3,3-Dichlor-Propan und Methyl Ter-Butyl-Aether enthaltende Reinigungsmittelzusammensetzung Download PDFInfo
- Publication number
- EP0456551A1 EP0456551A1 EP19910401135 EP91401135A EP0456551A1 EP 0456551 A1 EP0456551 A1 EP 0456551A1 EP 19910401135 EP19910401135 EP 19910401135 EP 91401135 A EP91401135 A EP 91401135A EP 0456551 A1 EP0456551 A1 EP 0456551A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pentafluoro
- butyl ether
- dichloro
- propane
- composition according
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 33
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 title claims abstract description 22
- 238000004140 cleaning Methods 0.000 title claims abstract description 13
- COAUHYBSXMIJDK-UHFFFAOYSA-N 3,3-dichloro-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)(F)C(F)(F)C(Cl)Cl COAUHYBSXMIJDK-UHFFFAOYSA-N 0.000 title claims abstract 6
- 238000005238 degreasing Methods 0.000 claims abstract description 6
- 150000001875 compounds Chemical group 0.000 claims abstract description 4
- 239000007787 solid Substances 0.000 claims abstract description 4
- 238000009835 boiling Methods 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- LYGJENNIWJXYER-BJUDXGSMSA-N nitromethane Chemical group [11CH3][N+]([O-])=O LYGJENNIWJXYER-BJUDXGSMSA-N 0.000 claims 1
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 abstract description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- 230000004907 flux Effects 0.000 description 6
- 229910000679 solder Inorganic materials 0.000 description 4
- 238000004821 distillation Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000012808 vapor phase Substances 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000007605 air drying Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000009304 pastoral farming Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 238000012795 verification Methods 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
- C11D7/5077—Mixtures of only oxygen-containing solvents
- C11D7/5086—Mixtures of only oxygen-containing solvents the oxygen-containing solvents being different from alcohols, e.g. mixtures of water and ethers
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G5/00—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
- C23G5/02—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
- C23G5/028—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing halogenated hydrocarbons
- C23G5/02809—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
Definitions
- the present invention relates to the field of chlorofluorinated hydrocarbons and more particularly relates to a new composition having an azeotrope and usable as an agent for cleaning and degreasing solid surfaces, in particular in defluxing and cold cleaning of printed circuits.
- 1,1,2-Trichloro-1,2,2-trifluoroethane (known in the art under the designation F113) is widely used in the industry for cleaning and degreasing solid surfaces.
- F113 1,1,2-Trichloro-1,2,2-trifluoroethane
- F113 1,1,2-Trichloro-1,2,2-trifluoroethane
- F113 is most often combined with other organic solvents (for example methanol), preferably in the form of azeotropic or pseudo-azeotropic mixtures which do not demix and which, when used at reflux, have substantially the same composition in the vapor phase as in the liquid phase.
- organic solvents for example methanol
- F113 is one of the fully halogenated chlorofluorocarbons that are currently suspected of attacking or degrading stratospheric ozone.
- the present invention proposes to replace the compositions based on F113 with a new composition based on methyl tert-butyl ether (hereinafter MTBE) and 1,1,1,2,2-pentafluoro. -3,3-dichloro-propane.
- MTBE methyl tert-butyl ether
- This latter compound known in the art under the designation 225ca, is practically devoid of destructive effect with respect to ozone.
- the composition to be used according to the invention comprises from 55 to 80% by weight of 225ca and from 20 to 45% of MTBE.
- azeotrope whose temperature boiling point is 59.9 ° C. at normal atmospheric pressure (1.013 bar) and the composition according to the invention has a pseudo-azeotropic behavior, that is to say that the composition of the vapor and liquid phases is substantially the same, which is particularly advantageous for the intended applications.
- the 225ca content is chosen between 62 and 67% by weight and that of MTBE between 38 and 33% by weight.
- the 225ca / MTBE azeotrope is a negative azeotrope since its boiling point (59.9 ° C) is higher than that of the two constituents (225ca: 51.1 ° C; MTBE: 54 ° C).
- the composition according to the invention can be advantageously stabilized against hydrolysis and / or free radical attacks likely to occur in the cleaning processes, by adding to it a usual stabilizer such as, for example , nitromethane, propylene oxide or a mixture of these compounds, the proportion of stabilizer can range from 0.01 to 5% relative to the total weight: 225ca + MTBE.
- a usual stabilizer such as, for example , nitromethane, propylene oxide or a mixture of these compounds
- composition according to the invention can be used in the same applications and according to the same techniques as the previous compositions based on F113.
- This azeotrope used for cleaning solder flux or degreasing mechanical parts, gives as good results as compositions based on F113 and methanol.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Detergent Compositions (AREA)
- Manufacturing Of Printed Wiring (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9005807A FR2661918B1 (fr) | 1990-05-10 | 1990-05-10 | Composition nettoyante a base de 1,1,1,2,2-pentafluoro-3,3-dichloro-propane et de methyl tert-butyl ether. |
| FR9005807 | 1990-05-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0456551A1 true EP0456551A1 (de) | 1991-11-13 |
Family
ID=9396451
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19910401135 Withdrawn EP0456551A1 (de) | 1990-05-10 | 1991-04-29 | 1,1,1,2,2-Pentafluor-3,3-Dichlor-Propan und Methyl Ter-Butyl-Aether enthaltende Reinigungsmittelzusammensetzung |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US5102563A (de) |
| EP (1) | EP0456551A1 (de) |
| JP (1) | JPH04227799A (de) |
| CA (1) | CA2040980A1 (de) |
| FR (1) | FR2661918B1 (de) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR970002043B1 (ko) * | 1989-02-01 | 1997-02-21 | 아사히 가라스 가부시끼가이샤 | 히드로클로로플루오로카본 공비 또는 공비형 혼합물 |
| IE66347B1 (en) * | 1989-10-06 | 1995-12-27 | Allied Signal Inc | Azeotrope-like compositions of dichloropentafluoropropane and a hydrocarbon containing sex carbon atoms |
| IE902926A1 (en) * | 1989-10-06 | 1991-04-10 | Allied Signal Inc | Azeotrope-like compositions of dichloropentafluoropropane¹and 1,2-dichloroethylene |
| US5494601A (en) * | 1993-04-01 | 1996-02-27 | Minnesota Mining And Manufacturing Company | Azeotropic compositions |
| US5578137A (en) * | 1993-08-31 | 1996-11-26 | E. I. Du Pont De Nemours And Company | Azeotropic or azeotrope-like compositions including 1,1,1,2,3,4,4,5,5,5-decafluoropentane |
| US6048471A (en) * | 1997-07-18 | 2000-04-11 | Richard G. Henry | Zero volatile organic compound compositions based upon organic solvents which are negligibly reactive with hydroxyl radical and do not contribute appreciably to the formation of ground based ozone |
| US6306943B1 (en) | 1997-07-18 | 2001-10-23 | Polymer Solvents, Llc | Zero volitile organic solvent compositions |
| WO2016154487A1 (en) * | 2015-03-24 | 2016-09-29 | Gestalt Sciences Corporation | Compositions, devices, systems and methods relating to photo- and thermal- oxidative bleaching of pink-stains |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2128555A1 (de) * | 1971-03-03 | 1972-10-20 | Ici Ltd | |
| EP0258079A1 (de) * | 1986-07-21 | 1988-03-02 | Elf Atochem S.A. | Methylenchloridzusammensetzung und deren Verwendung für die Photolackentschichtung |
| EP0347924A1 (de) * | 1988-06-22 | 1989-12-27 | Asahi Glass Company Ltd. | Verwendung von Halogenkohlenwasserstofflösungsmittel als Reinigungsmittel |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR970002043B1 (ko) * | 1989-02-01 | 1997-02-21 | 아사히 가라스 가부시끼가이샤 | 히드로클로로플루오로카본 공비 또는 공비형 혼합물 |
| JPH02202998A (ja) * | 1989-02-02 | 1990-08-13 | Asahi Glass Co Ltd | 混合溶剤組成物 |
| JP2692233B2 (ja) * | 1989-02-03 | 1997-12-17 | 旭硝子株式会社 | 弗素化炭化水素系混合溶剤組成物 |
| DE69019183D1 (de) * | 1989-02-06 | 1995-06-14 | Asahi Glass Co Ltd | Azeotrope oder azeotropähnliche Zusammensetzung auf der Basis von Wasserstoff enthaltenden Chlorfluorkohlenwasserstoffen. |
| US4947881A (en) * | 1989-02-24 | 1990-08-14 | Allied-Signal Inc. | Method of cleaning using hydrochlorofluorocarbons |
| US4961869A (en) * | 1989-08-03 | 1990-10-09 | E. I. Du Pont De Nemours And Company | Ternary azeotropic compositions of 2,3-dichloro-1,1,1,3,3-pentafluoropropane with trans-1,2-dichloroethylene and methanol |
| IE64912B1 (en) * | 1989-10-06 | 1995-09-20 | Allied Signal Inc | Azetrope-like compositions of 1,3-dichloro-1,1,2,2,3-pentafluoropropane and 2-methyl-2-propanol |
| US4970013A (en) * | 1989-12-11 | 1990-11-13 | E. I. Dupont De Nemours And Company | Binary azeotropic composition of 2,3-dichloro-1,1,1,3-3-pentafluoropropane and methanol |
-
1990
- 1990-05-10 FR FR9005807A patent/FR2661918B1/fr not_active Expired - Lifetime
-
1991
- 1991-04-23 CA CA002040980A patent/CA2040980A1/fr not_active Abandoned
- 1991-04-29 EP EP19910401135 patent/EP0456551A1/de not_active Withdrawn
- 1991-05-10 US US07/698,021 patent/US5102563A/en not_active Expired - Fee Related
- 1991-05-10 JP JP3106018A patent/JPH04227799A/ja active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2128555A1 (de) * | 1971-03-03 | 1972-10-20 | Ici Ltd | |
| EP0258079A1 (de) * | 1986-07-21 | 1988-03-02 | Elf Atochem S.A. | Methylenchloridzusammensetzung und deren Verwendung für die Photolackentschichtung |
| EP0347924A1 (de) * | 1988-06-22 | 1989-12-27 | Asahi Glass Company Ltd. | Verwendung von Halogenkohlenwasserstofflösungsmittel als Reinigungsmittel |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2040980A1 (fr) | 1991-11-11 |
| US5102563A (en) | 1992-04-07 |
| FR2661918B1 (fr) | 1992-07-17 |
| FR2661918A1 (fr) | 1991-11-15 |
| JPH04227799A (ja) | 1992-08-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 19910504 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): BE DE ES FR GB IT NL |
|
| RAP3 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: ELF ATOCHEM S.A. |
|
| 17Q | First examination report despatched |
Effective date: 19941115 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
| 18D | Application deemed to be withdrawn |
Effective date: 19950517 |