AU609363B2 - Stabilized azeotrope of azeotrope-like composition of 1,1,2-trichloro-1,2,22-trifluorethane and trans 1, 2-dichloroethylene - Google Patents
Stabilized azeotrope of azeotrope-like composition of 1,1,2-trichloro-1,2,22-trifluorethane and trans 1, 2-dichloroethylene Download PDFInfo
- Publication number
- AU609363B2 AU609363B2 AU28965/89A AU2896589A AU609363B2 AU 609363 B2 AU609363 B2 AU 609363B2 AU 28965/89 A AU28965/89 A AU 28965/89A AU 2896589 A AU2896589 A AU 2896589A AU 609363 B2 AU609363 B2 AU 609363B2
- Authority
- AU
- Australia
- Prior art keywords
- composition
- solvent
- weight percent
- concentration
- present
- 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.)
- Ceased
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- 239000000203 mixture Substances 0.000 title claims description 45
- KFUSEUYYWQURPO-OWOJBTEDSA-N trans-1,2-dichloroethene Chemical group Cl\C=C\Cl KFUSEUYYWQURPO-OWOJBTEDSA-N 0.000 title claims description 18
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 claims description 25
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 23
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 claims description 15
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 claims description 13
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 claims description 12
- 230000000087 stabilizing effect Effects 0.000 claims description 10
- 239000002904 solvent Substances 0.000 description 52
- 238000004140 cleaning Methods 0.000 description 15
- 238000009835 boiling Methods 0.000 description 14
- 230000004907 flux Effects 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 7
- 239000011877 solvent mixture Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 230000007797 corrosion Effects 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000005476 soldering Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 229910000838 Al alloy Inorganic materials 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- -1 amine hydrochlorides Chemical class 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000002274 desiccant Substances 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229910000679 solder Inorganic materials 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- HLHGWZFLOVNPGQ-WLHGVMLRSA-N (e)-1,2-dichloroethene;1,1,2-trichloro-1,2,2-trifluoroethane Chemical compound Cl\C=C\Cl.FC(F)(Cl)C(F)(Cl)Cl HLHGWZFLOVNPGQ-WLHGVMLRSA-N 0.000 description 1
- MOEFFSWKSMRFRQ-UHFFFAOYSA-N 2-ethoxyphenol Chemical compound CCOC1=CC=CC=C1O MOEFFSWKSMRFRQ-UHFFFAOYSA-N 0.000 description 1
- JFSVGKRARHIICJ-UHFFFAOYSA-N 2-propoxyphenol Chemical compound CCCOC1=CC=CC=C1O JFSVGKRARHIICJ-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
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 101100521097 Caenorhabditis elegans pri-1 gene Proteins 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241001482237 Pica Species 0.000 description 1
- 101100269495 Rattus norvegicus Ina gene Proteins 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
- 230000003213 activating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002912 oxalic acid derivatives Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000013112 stability test 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
- 230000008016 vaporization Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Manufacturing Of Printed Wiring (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/198,015 US4804493A (en) | 1988-05-24 | 1988-05-24 | Stabilized azeotrope or azeotrope-like composition of 1,1,2-trichloro-1,2,2-trifluoroethane and trans-1,2-dichloroethylene |
| US198015 | 2002-07-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2896589A AU2896589A (en) | 1989-11-30 |
| AU609363B2 true AU609363B2 (en) | 1991-04-26 |
Family
ID=22731641
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU28965/89A Ceased AU609363B2 (en) | 1988-05-24 | 1989-02-01 | Stabilized azeotrope of azeotrope-like composition of 1,1,2-trichloro-1,2,22-trifluorethane and trans 1, 2-dichloroethylene |
Country Status (9)
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4767561A (en) * | 1987-09-23 | 1988-08-30 | E. I. Du Pont De Nemours And Company | Azeotrope or azeotrope-like composition of trichlorotrifluoroethane, methanol and 1,2-dichloroethylene |
| ATE87983T1 (de) * | 1988-02-02 | 1993-04-15 | Du Pont | Azeotrope oder azeotropaehnliche stabilisierte zusammensetzung von 1,1,2-trichlor-1,2,2trifluorethan, methanol und 1,2-dichloroethylen. |
| US4992604A (en) * | 1989-07-24 | 1991-02-12 | Ppg Industries, Inc. | Stabilized 1,1,1-trichloroethane compositions |
| US5035831A (en) * | 1989-10-06 | 1991-07-30 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1,2-trichloro-1,2,2-trifluoroethane, nitromethane, 1,2-dichloroethylene, and ethanol or isopropanol |
| US4961870A (en) * | 1989-12-14 | 1990-10-09 | Allied-Signal Inc. | Azeotrope-like compositions of 1,1,2-trichloro-1,2,2-trifluoroethane,1,2-dichloroethylene, and alkanol having 3 to 7 carbon atoms |
| FR2657876B1 (fr) * | 1990-02-07 | 1992-05-15 | Atochem | Composition nettoyante a base de 1,1-dichloro-1-fluoroethane et de formiate de methyle. |
| FR2657877B1 (fr) * | 1990-02-07 | 1992-05-15 | Atochem | Composition nettoyante a base de 1,1-dichloro-1-fluoroethane, de formiate de methyle et de methanol. |
| US5114608A (en) * | 1990-10-12 | 1992-05-19 | Baxter International Inc. | Method of cleaning hollow fiber components of a dialyzer with chloro fluorocarbon compositions stabilized by epoxidized fatty acid glycerides or esters |
| EP0927240A1 (en) | 1996-05-03 | 1999-07-07 | The Procter & Gamble Company | Detergent compositions comprising polyamine polymers with improved soil dispersancy |
| US6534688B2 (en) | 2001-06-11 | 2003-03-18 | Vulcan Chemicals | Dehydrochlorination stabilization of polychlorinated alkanes |
| US6500995B1 (en) | 2001-06-14 | 2002-12-31 | Vulcan Chemicals | Water-enhanced production of 1,1,1,3,3,-pentachloropropane |
| FR2861390B1 (fr) * | 2003-10-24 | 2006-01-21 | Arkema | Stabilisation du trans-1,2-dichlorethylene |
| US7390777B2 (en) * | 2004-02-13 | 2008-06-24 | Ppg Industries Ohio, Inc. | 1,2-dichloroethylene compositions |
| EP1700904A1 (en) | 2005-03-11 | 2006-09-13 | Unilever N.V. | Liquid detergent composition |
| EP1700907A1 (en) | 2005-03-11 | 2006-09-13 | Unilever N.V. | Liquid bleaching composition |
| CN101432400B (zh) * | 2006-05-01 | 2012-11-14 | 国际壳牌研究有限公司 | 气化反应器及其应用 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2896489A (en) * | 1988-02-02 | 1989-08-03 | E.I. Du Pont De Nemours And Company | Stabilized azeotrope or azeotrope-like composition of 1,1,2- trichloro-1,2,2-trifluoroethane, methanol and 1,2-dichloroethylene |
| AU590334B2 (en) * | 1985-10-02 | 1989-11-02 | Allied Corporation | Azeotrope-like compositions of trichlorotrifluoroethane, methanol, nitromethane and hexane |
| AU601927B2 (en) * | 1987-09-23 | 1990-09-20 | E.I. Du Pont De Nemours And Company | An azeotrope or azeotrope-like composition of trichlorotrifluoroethane, methanol and 1, 2-dichloroethylene |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE633999A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1962-06-26 | |||
| GB989155A (en) * | 1964-03-31 | 1965-04-14 | Ici Ltd | Solvent compositions |
| US3455835A (en) * | 1966-04-12 | 1969-07-15 | Du Pont | Azeotropic composition |
| GB1288565A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1969-03-24 | 1972-09-13 | ||
| NL7103446A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1970-03-18 | 1971-09-21 |
-
1988
- 1988-05-24 US US07/198,015 patent/US4804493A/en not_active Expired - Fee Related
-
1989
- 1989-01-27 IN IN86/CAL/89A patent/IN171552B/en unknown
- 1989-01-30 BR BR898900369A patent/BR8900369A/pt unknown
- 1989-01-30 EP EP89300861A patent/EP0343761A1/en not_active Withdrawn
- 1989-01-30 MY MYPI89000113A patent/MY103506A/en unknown
- 1989-01-31 KR KR1019890001115A patent/KR890018023A/ko not_active Withdrawn
- 1989-02-01 AU AU28965/89A patent/AU609363B2/en not_active Ceased
- 1989-02-01 CN CN89100718A patent/CN1037920A/zh active Granted
- 1989-02-01 JP JP1023639A patent/JPH02150499A/ja active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU590334B2 (en) * | 1985-10-02 | 1989-11-02 | Allied Corporation | Azeotrope-like compositions of trichlorotrifluoroethane, methanol, nitromethane and hexane |
| AU601927B2 (en) * | 1987-09-23 | 1990-09-20 | E.I. Du Pont De Nemours And Company | An azeotrope or azeotrope-like composition of trichlorotrifluoroethane, methanol and 1, 2-dichloroethylene |
| AU2896489A (en) * | 1988-02-02 | 1989-08-03 | E.I. Du Pont De Nemours And Company | Stabilized azeotrope or azeotrope-like composition of 1,1,2- trichloro-1,2,2-trifluoroethane, methanol and 1,2-dichloroethylene |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2896589A (en) | 1989-11-30 |
| BR8900369A (pt) | 1990-03-01 |
| IN171552B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1992-11-21 |
| EP0343761A1 (en) | 1989-11-29 |
| KR890018023A (ko) | 1989-12-18 |
| MY103506A (en) | 1993-06-30 |
| JPH02150499A (ja) | 1990-06-08 |
| US4804493A (en) | 1989-02-14 |
| CN1037920A (zh) | 1989-12-13 |
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