JPS6210213B2 - - Google Patents
Info
- Publication number
- JPS6210213B2 JPS6210213B2 JP52027129A JP2712977A JPS6210213B2 JP S6210213 B2 JPS6210213 B2 JP S6210213B2 JP 52027129 A JP52027129 A JP 52027129A JP 2712977 A JP2712977 A JP 2712977A JP S6210213 B2 JPS6210213 B2 JP S6210213B2
- Authority
- JP
- Japan
- Prior art keywords
- vinyl ether
- fluoro
- solution
- vapor
- alkyl vinyl
- 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.)
- Expired
Links
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 51
- 238000006116 polymerization reaction Methods 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 40
- 239000000110 cooling liquid Substances 0.000 claims description 30
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 29
- -1 alkyl vinyl ether Chemical compound 0.000 claims description 26
- 125000001153 fluoro group Chemical group F* 0.000 claims description 25
- 238000001816 cooling Methods 0.000 claims description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- OVGRCEFMXPHEBL-UHFFFAOYSA-N 1-ethenoxypropane Chemical compound CCCOC=C OVGRCEFMXPHEBL-UHFFFAOYSA-N 0.000 claims description 18
- 239000007788 liquid Substances 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 14
- 238000007710 freezing Methods 0.000 claims description 11
- 230000008014 freezing Effects 0.000 claims description 11
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 10
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 10
- 239000001110 calcium chloride Substances 0.000 claims description 10
- 235000011148 calcium chloride Nutrition 0.000 claims description 10
- 239000002826 coolant Substances 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 3
- 239000002904 solvent Substances 0.000 description 38
- 239000000243 solution Substances 0.000 description 31
- 238000011084 recovery Methods 0.000 description 27
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 17
- 239000012071 phase Substances 0.000 description 15
- JMGNVALALWCTLC-UHFFFAOYSA-N 1-fluoro-2-(2-fluoroethenoxy)ethene Chemical compound FC=COC=CF JMGNVALALWCTLC-UHFFFAOYSA-N 0.000 description 14
- 229920001577 copolymer Polymers 0.000 description 12
- 238000002474 experimental method Methods 0.000 description 11
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 11
- 239000000178 monomer Substances 0.000 description 10
- 239000007789 gas Substances 0.000 description 9
- 238000000926 separation method Methods 0.000 description 9
- 239000007791 liquid phase Substances 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000012986 chain transfer agent Substances 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 238000010908 decantation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000005086 pumping Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000012808 vapor phase Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 230000002269 spontaneous effect Effects 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- AEDZKIACDBYJLQ-UHFFFAOYSA-N ethane-1,2-diol;hydrate Chemical compound O.OCCO AEDZKIACDBYJLQ-UHFFFAOYSA-N 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/667,278 US4042634A (en) | 1976-03-15 | 1976-03-15 | Fluorocarbon separation process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS52111507A JPS52111507A (en) | 1977-09-19 |
| JPS6210213B2 true JPS6210213B2 (enExample) | 1987-03-05 |
Family
ID=24677573
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2712977A Granted JPS52111507A (en) | 1976-03-15 | 1977-03-14 | Method of separation of fluorocarbon |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4042634A (enExample) |
| JP (1) | JPS52111507A (enExample) |
| DE (1) | DE2711243A1 (enExample) |
| FR (1) | FR2344517A1 (enExample) |
| GB (1) | GB1514700A (enExample) |
| IT (1) | IT1075671B (enExample) |
| NL (1) | NL7702783A (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3015092A1 (de) * | 1980-04-19 | 1981-10-22 | Hoechst Ag, 6000 Frankfurt | Verfahren zur abtrennung von tetrafluorethylen aus gasgemischen, die insbesondere stickstoff oder kohlenmonoxid enthalten |
| JP2610538B2 (ja) * | 1990-04-13 | 1997-05-14 | 日本メクトロン株式会社 | パーフルオロ（プロピルビニルエーテル）の精製法 |
| IT1264662B1 (it) * | 1993-07-05 | 1996-10-04 | Ausimont Spa | Perflurodiossoli loro omopolimeri e copolimeri e loro impiego per il rivestimento di cavi elettrici |
| IT1264661B1 (it) * | 1993-07-05 | 1996-10-04 | Ausimont Spa | Copolimeri termoprocessabilin del tetrafluoroetilene |
| IT1272863B (it) * | 1995-01-04 | 1997-07-01 | Ausimont Spa | Copolimeri termoprocessabili del tetrafluoroetilene |
| IT1299036B1 (it) | 1998-04-07 | 2000-02-07 | Ausimont Spa | Purificazione del perfluoropropilviniletere |
| US7534845B2 (en) | 2000-04-21 | 2009-05-19 | Solvay Solexis S.P.A. | Fluorovinyl ethers and polymers obtainable therefrom |
| IT1318488B1 (it) | 2000-04-21 | 2003-08-25 | Ausimont Spa | Fluorovinileteri e polimeri da essi ottenibili. |
| IT1318487B1 (it) | 2000-04-21 | 2003-08-25 | Ausimont Spa | Fluoroelastomeri. |
| US7723447B2 (en) * | 2002-12-20 | 2010-05-25 | Exxonmobil Chemical Patents Inc. | Polymerization processes |
| AU2003297458A1 (en) * | 2002-12-20 | 2004-07-22 | Exxonmobil Chemical Patents Inc. | Polymerization processes |
| US7425601B2 (en) * | 2002-12-20 | 2008-09-16 | Exxonmobil Chemical Patents Inc. | Polymers with new sequence distributions |
| EP1572763B1 (en) * | 2002-12-20 | 2010-05-26 | ExxonMobil Chemical Patents Inc. | Polymers with new sequence distributions |
| JP4292914B2 (ja) | 2003-08-07 | 2009-07-08 | パナソニック株式会社 | 携帯受信装置とこれに用いる分波器 |
| WO2006009942A1 (en) * | 2004-06-21 | 2006-01-26 | Exxonmobil Chemical Patents Inc. | Polymerization process |
| WO2006009945A1 (en) | 2004-06-21 | 2006-01-26 | Exxonmobil Chemical Patents Inc. | Impact copolymers |
| WO2006083303A1 (en) * | 2004-06-21 | 2006-08-10 | Exxonmobil Chemical Patents Inc. | Polymerization process |
| WO2006009951A1 (en) * | 2004-06-21 | 2006-01-26 | Exxonmobil Chemical Patents Inc. | Polymer recovery method |
| ITMI20041573A1 (it) | 2004-07-30 | 2006-01-31 | Solvay Solexis Spa | Fluoroelastomeri |
| ITMI20041572A1 (it) | 2004-07-30 | 2004-10-30 | Solvay Solexis Spa | Capolimeri termoprocessabili a base di tfe |
| US7799882B2 (en) * | 2005-06-20 | 2010-09-21 | Exxonmobil Chemical Patents Inc. | Polymerization process |
| WO2020187839A1 (en) * | 2019-03-18 | 2020-09-24 | Solvay Specialty Polymers Italy S.P.A. | Heat exchange method using fluorinated compounds having a low gwp |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3635926A (en) * | 1969-10-27 | 1972-01-18 | Du Pont | Aqueous process for making improved tetrafluoroethylene / fluoroalkyl perfluorovinyl ether copolymers |
-
1976
- 1976-03-15 US US05/667,278 patent/US4042634A/en not_active Expired - Lifetime
-
1977
- 1977-03-11 GB GB10461/77A patent/GB1514700A/en not_active Expired
- 1977-03-14 JP JP2712977A patent/JPS52111507A/ja active Granted
- 1977-03-14 FR FR7707489A patent/FR2344517A1/fr active Granted
- 1977-03-14 IT IT21213/77A patent/IT1075671B/it active
- 1977-03-15 DE DE19772711243 patent/DE2711243A1/de not_active Ceased
- 1977-03-15 NL NL7702783A patent/NL7702783A/xx not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| FR2344517B1 (enExample) | 1983-08-19 |
| DE2711243A1 (de) | 1977-09-29 |
| JPS52111507A (en) | 1977-09-19 |
| FR2344517A1 (fr) | 1977-10-14 |
| US4042634A (en) | 1977-08-16 |
| GB1514700A (en) | 1978-06-21 |
| IT1075671B (it) | 1985-04-22 |
| NL7702783A (nl) | 1977-09-19 |
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