JP2004504283A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2004504283A5 JP2004504283A5 JP2002512100A JP2002512100A JP2004504283A5 JP 2004504283 A5 JP2004504283 A5 JP 2004504283A5 JP 2002512100 A JP2002512100 A JP 2002512100A JP 2002512100 A JP2002512100 A JP 2002512100A JP 2004504283 A5 JP2004504283 A5 JP 2004504283A5
- Authority
- JP
- Japan
- Prior art keywords
- gold
- reaction zone
- reactant
- moiety
- reactor
- 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.)
- Granted
Links
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 26
- 238000000034 method Methods 0.000 description 22
- 229910052737 gold Inorganic materials 0.000 description 21
- 239000010931 gold Substances 0.000 description 21
- 239000000376 reactant Substances 0.000 description 21
- 238000006243 chemical reaction Methods 0.000 description 19
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 13
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 10
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 10
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 10
- 229910001026 inconel Inorganic materials 0.000 description 8
- 238000010791 quenching Methods 0.000 description 8
- 238000000197 pyrolysis Methods 0.000 description 7
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- JQZFYIGAYWLRCC-UHFFFAOYSA-N 1-chloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)C(F)(F)Cl JQZFYIGAYWLRCC-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 150000001722 carbon compounds Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- DAFIBNSJXIGBQB-UHFFFAOYSA-N perfluoroisobutene Chemical group FC(F)=C(C(F)(F)F)C(F)(F)F DAFIBNSJXIGBQB-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000003682 fluorination reaction Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21833800P | 2000-07-14 | 2000-07-14 | |
| US60/218,338 | 2000-07-14 | ||
| US27138701P | 2001-02-26 | 2001-02-26 | |
| US60/271,387 | 2001-02-26 | ||
| US09/878,540 | 2001-06-11 | ||
| US09/878,540 US20020032356A1 (en) | 2000-07-14 | 2001-06-11 | Synthesis of perfluoroolefins |
| PCT/US2001/022234 WO2002006193A2 (en) | 2000-07-14 | 2001-07-13 | Synthesis of perfluoroolefins |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004504283A JP2004504283A (ja) | 2004-02-12 |
| JP2004504283A5 true JP2004504283A5 (https=) | 2008-09-04 |
| JP4926365B2 JP4926365B2 (ja) | 2012-05-09 |
Family
ID=27396530
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002512100A Expired - Fee Related JP4926365B2 (ja) | 2000-07-14 | 2001-07-13 | パーフルオロオレフィンの合成 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US20020032356A1 (https=) |
| EP (1) | EP1301453B1 (https=) |
| JP (1) | JP4926365B2 (https=) |
| CN (1) | CN1217895C (https=) |
| DE (1) | DE60142051D1 (https=) |
| WO (1) | WO2002006193A2 (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7655610B2 (en) * | 2004-04-29 | 2010-02-02 | Honeywell International Inc. | Blowing agent compositions comprising fluorinated olefins and carbon dioxide |
| US6958422B2 (en) * | 2003-12-17 | 2005-10-25 | E. I. Du Pont De Nemours And Company | Pyrolysis process |
| US20060116538A1 (en) * | 2004-10-29 | 2006-06-01 | Ralph Newton Miller | Azeotrope compositions comprising 1,1,3,3,3-pentafluoropropene and hydrogen fluoride and uses thereof |
| US20060094911A1 (en) * | 2004-10-29 | 2006-05-04 | Rao Velliyur N M | Noncatalytic manufacture of 1,1,3,3,3-pentafluoropropene from 1,1,1,3,3,3-hexafluoropropane |
| US7897823B2 (en) * | 2004-10-29 | 2011-03-01 | E. I. Du Pont De Nemours And Company | Process for production of azeotrope compositions comprising hydrofluoroolefin and hydrogen fluoride and uses of said azeotrope compositions in separation processes |
| CN101351430A (zh) * | 2005-11-03 | 2009-01-21 | 霍尼韦尔国际公司 | 氟化有机化合物的制备方法 |
| JP5393454B2 (ja) * | 2006-06-27 | 2014-01-22 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 1,2,3,3,3−ペンタフルオロプロペンの製造方法 |
| GB201010958D0 (en) * | 2010-06-30 | 2010-08-11 | 3M Innovative Properties Co | Process for manufacturing perfluoroolefins by pyrolysis of perfluorocarbons in the presence of hydrogen |
| JP2016013994A (ja) * | 2014-07-03 | 2016-01-28 | 日華化学株式会社 | テトラフルオロエチレン及び/又はヘキサフルオロプロピレンの製造方法 |
| CN110420572A (zh) * | 2019-08-29 | 2019-11-08 | 江西理文化工有限公司 | 一种新型生产六氟丙烯裂解系统 |
| WO2021093029A1 (en) | 2019-11-13 | 2021-05-20 | Fujian Yongjing Technology Co., Ltd | New process for synthesis of 2,3,3,3-tetrafluoropropene (1234yf) and 2,3-dichloro-1,1,1-trifluoropropane (243db) |
| JP7011268B2 (ja) | 2020-02-28 | 2022-01-26 | ダイキン工業株式会社 | ハイドロフルオロオレフィン又はフルオロオレフィンの製造方法 |
| CN114956953B (zh) * | 2022-06-21 | 2024-09-27 | 常熟三爱富氟化工有限责任公司 | 制备六氟丙烯的工艺 |
| EP4588907A1 (en) * | 2022-09-16 | 2025-07-23 | Agc Inc. | Fluoroolefin production method |
| CN121013831A (zh) * | 2023-04-26 | 2025-11-25 | Agc株式会社 | 氟烯烃的制造方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL67177C (https=) | 1939-07-01 | 1900-01-01 | ||
| BE463585A (https=) | 1942-07-23 | |||
| US2551573A (en) | 1945-11-30 | 1951-05-08 | Du Pont | Pyrolysis of chloro-fluoro alkanes |
| US2758138A (en) | 1954-05-06 | 1956-08-07 | Du Pont | Pyrolysis process for making perfluoropropene from tetrafluoroethylene |
| US2970176A (en) | 1957-10-31 | 1961-01-31 | Du Pont | Pyrolysis of fluorocarbons to hexafluoropropylene |
| DE1068695B (de) * | 1958-02-06 | 1959-11-12 | Farbwerke Hoechst Aktiengesellschaft vormals Meister Lucius 6. Brüning, Frankfurt/M | Verfahren zur Herstellung von Fluoräthylenen |
| NL122622C (https=) * | 1960-09-28 | |||
| US3446858A (en) | 1963-03-30 | 1969-05-27 | Daikin Ind Ltd | Process for the manufacture of hexafluoropropene |
| US3397248A (en) | 1964-05-15 | 1968-08-13 | Du Pont | Process for the preparation of hexafluoropropene |
| DE1236497B (de) | 1965-02-02 | 1967-03-16 | Fluorwerke Dohna | Verfahren zur Herstellung von Perfluorpropen |
| US3459818A (en) | 1966-05-28 | 1969-08-05 | Asahi Glass Co Ltd | Process of producing tetrafluoroethylene and hexafluoropropylene |
| US3873630A (en) | 1972-06-12 | 1975-03-25 | Du Pont | Process for pyrolyzing tetrafluoroethylene to hexafluoropropylene |
| US5334783A (en) | 1988-03-14 | 1994-08-02 | Hoechst Aktiengesellschaft | Process for the preparation of hexafluoropropene |
| DE58904105D1 (de) | 1988-03-14 | 1993-05-27 | Hoechst Ag | Verfahren zur herstellung von hexafluorpropen. |
| JPH08501551A (ja) * | 1992-09-22 | 1996-02-20 | イー・アイ・デュポン・ドゥ・ヌムール・アンド・カンパニー | 高度にフッ素化されたアルカンの製造のための耐蝕性装置 |
| WO1995024369A1 (en) | 1994-03-11 | 1995-09-14 | E.I. Du Pont De Nemours And Company | Process for converting chlorodifluoromethane and/or dichlorodifluoromethane |
| US5705719A (en) | 1996-08-01 | 1998-01-06 | E. I. Du Pont De Nemours And Company | Selective removal of perfluoroisobutylene from streams of halogenated hydrocarbons |
| FR2758556B1 (fr) * | 1997-01-17 | 1999-02-19 | Atochem Elf Sa | Isomerisation d'hydrofluorocarbures |
| CN1213974C (zh) * | 1999-06-04 | 2005-08-10 | 纳幕尔杜邦公司 | 生产氟代烯烃的方法 |
-
2001
- 2001-06-11 US US09/878,540 patent/US20020032356A1/en not_active Abandoned
- 2001-07-13 DE DE60142051T patent/DE60142051D1/de not_active Expired - Lifetime
- 2001-07-13 EP EP01952749A patent/EP1301453B1/en not_active Expired - Lifetime
- 2001-07-13 JP JP2002512100A patent/JP4926365B2/ja not_active Expired - Fee Related
- 2001-07-13 CN CN018128289A patent/CN1217895C/zh not_active Expired - Fee Related
- 2001-07-13 WO PCT/US2001/022234 patent/WO2002006193A2/en not_active Ceased
-
2006
- 2006-02-22 US US11/359,807 patent/US7271301B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2004504283A5 (https=) | ||
| JP5532131B2 (ja) | 1,1,2,3−テトラクロロプロペンの製造方法 | |
| JP4425636B2 (ja) | フルオロホルム(hfc−23)の処理 | |
| JP4547256B2 (ja) | ヘキサフルオロプロピレンの合成 | |
| US9061957B2 (en) | Method for producing fluorinated organic compounds | |
| JP4926365B2 (ja) | パーフルオロオレフィンの合成 | |
| JP5715177B2 (ja) | フッ素化有機化合物の製造方法 | |
| EP1084092B1 (en) | Process for the production of hexafluoropropylene from cc1f2cc1fcf3 and azeotropes of cc1f2cc1fcf3 with hf | |
| KR20060060021A (ko) | 플루오로카본의 제조시스템 및 제조방법 | |
| JP2009518288A (ja) | フッ素化有機化合物の製造方法 | |
| JP2005515140A5 (https=) | ||
| JP2002316957A (ja) | パーフルオロアルキルアイオダイドテロマーの連続製造方法 | |
| CN113454052A (zh) | 卤化烯烃化合物和氟化炔烃化合物的制造方法 | |
| TWI289548B (en) | Process for production of hexafluorobutadiene and 1,2-dichlorohexafluorocyclobutane | |
| US2615925A (en) | Preparation of olefinic compounds | |
| KR102566765B1 (ko) | 시클로부텐의 제조 방법 | |
| EP1294663A1 (en) | Fluorinated benzene manufacturing process | |
| JP5601471B2 (ja) | 塩素含有フルオロプロペンの製造方法 | |
| JPH09506901A (ja) | フッ素化オレフィンの製造方法 | |
| JP4834558B2 (ja) | 熱分解方法 | |
| CN217313342U (zh) | 液相连续氟化反应器 | |
| JP2021008431A (ja) | アルカンの製造方法 | |
| KR20190069549A (ko) | 플루오르화 사이클로부탄의 제조 방법 | |
| JP2023056213A (ja) | 1,1-ジクロロ-3,3,3-トリフルオロプロペンの製造方法 | |
| JP2009143812A (ja) | ωハロゲノアルカンの製造方法 |