ES2547073T3 - Método para preparar 1,1-difluoroetano - Google Patents
Método para preparar 1,1-difluoroetano Download PDFInfo
- Publication number
- ES2547073T3 ES2547073T3 ES11000069.2T ES11000069T ES2547073T3 ES 2547073 T3 ES2547073 T3 ES 2547073T3 ES 11000069 T ES11000069 T ES 11000069T ES 2547073 T3 ES2547073 T3 ES 2547073T3
- Authority
- ES
- Spain
- Prior art keywords
- catalyst
- products
- reaction vessel
- hydrogen
- strong
- 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 - Lifetime
Links
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 239000000376 reactant Substances 0.000 abstract 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 abstract 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract 2
- 238000003682 fluorination reaction Methods 0.000 abstract 2
- 229910000040 hydrogen fluoride Inorganic materials 0.000 abstract 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 abstract 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002841 Lewis acid Substances 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000003213 activating effect Effects 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 150000008282 halocarbons Chemical class 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 239000011968 lewis acid catalyst Substances 0.000 abstract 1
- 150000007517 lewis acids Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/125—Halogens; Compounds thereof with scandium, yttrium, aluminium, gallium, indium or thallium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/20—Vanadium, niobium or tantalum
- B01J23/22—Vanadium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/08—Halides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/135—Halogens; Compounds thereof with titanium, zirconium, hafnium, germanium, tin or lead
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/22—Halogenating
- B01J37/26—Fluorinating
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/202—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
- C07C17/206—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being HX
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/202—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
- C07C17/208—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being MX
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/21—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms with simultaneous increase of the number of halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C19/00—Acyclic saturated compounds containing halogen atoms
- C07C19/08—Acyclic saturated compounds containing halogen atoms containing fluorine
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/18—Carbon
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
Un procedimiento para la producción de 1,1-difluoroetano (HFC-152a), comprendiendo el procedimiento: (a) proporcionar un recipiente de reacción, (b) proporcionar en el recipiente de reacción carbono activado impregnado con un catalizador de fluoración de ácido de Lewis fuerte, en el que el catalizador de ácido de Lewis fuerte se selecciona del grupo que consiste en haluros de Sb, (c) activar el catalizador haciendo pasar a través del carbono activado impregnado con un catalizador de fluoración de ácido de Lewis fuerte gas fluoruro de hidrógeno anhidro y gas cloro, (d) poner en contacto, en un estado de vapor en el recipiente de reacción que contiene el catalizador activado, fluoruro de hidrógeno y uno o más hidrocarburos halogenados seleccionados del grupo que consiste en cloruro de vinilo, 1,2-dicloroetano y 1,1-dicloroetano durante 1 a 120 segundos a 40 hasta 200 ºC para producir una corriente de producto que comprende producto o productos hidrofluorocarbonados correspondientes al o a los reaccionantes hidrocarbonados clorados, cloruro de hidrógeno, reaccionante o reaccionantes hidrocarbonados clorados que no han reaccionado, y fluoruro de hidrógeno que no ha reaccionado, y (e) separar el o los productos hidrofluorocarbonados de la corriente de producto.
Description
Claims (1)
-
imagen1 imagen2
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/816,447 US7112708B2 (en) | 2004-04-01 | 2004-04-01 | Method of making difluoromethane, 1,1,1-trifluoroethane and 1,1-difluoroethane |
| US816447 | 2004-04-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2547073T3 true ES2547073T3 (es) | 2015-10-01 |
Family
ID=34964830
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES05779894T Expired - Lifetime ES2386898T3 (es) | 2004-04-01 | 2005-03-31 | Método para fabricar difluorometano |
| ES11000069.2T Expired - Lifetime ES2547073T3 (es) | 2004-04-01 | 2005-03-31 | Método para preparar 1,1-difluoroetano |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES05779894T Expired - Lifetime ES2386898T3 (es) | 2004-04-01 | 2005-03-31 | Método para fabricar difluorometano |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7112708B2 (es) |
| EP (2) | EP2336101B1 (es) |
| JP (1) | JP4871261B2 (es) |
| KR (1) | KR101163528B1 (es) |
| CN (1) | CN100526271C (es) |
| AT (1) | ATE556043T1 (es) |
| ES (2) | ES2386898T3 (es) |
| WO (1) | WO2005097716A1 (es) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7608574B2 (en) * | 2006-08-17 | 2009-10-27 | Honeywell International Inc. | Azeotropic or azeotropic-like compositions of 1,1,1-trifuoroethane and 1-chloro-2,2,2-trifluoroethane |
| KR101270583B1 (ko) * | 2011-08-25 | 2013-06-03 | 한국과학기술연구원 | 초임계유체공정에 의한 클로로디플루오로메탄으로부터 디플루오로메탄을 제조하는 방법 |
| JP5807690B2 (ja) | 2013-04-25 | 2015-11-10 | ダイキン工業株式会社 | 含フッ素オレフィンの製造方法 |
| CN104140353A (zh) * | 2014-07-18 | 2014-11-12 | 江西格美氟化工有限公司 | 偏氯乙烯液相一步氟化制1,1,1-三氟乙烷的方法 |
| CN104785306B (zh) * | 2015-03-18 | 2017-12-22 | 巨化集团技术中心 | 一种气相裂解三氯乙烷制备顺式二氯乙烯的镁基催化剂的原位活化和评价方法 |
| CN112739673B (zh) * | 2018-08-24 | 2025-03-25 | 霍尼韦尔国际公司 | 用于产生三氟碘甲烷和三氟乙酰碘的方法 |
| CN109734550B (zh) * | 2019-02-25 | 2023-06-30 | 内蒙古永和氟化工有限公司 | 一种1,1-二氟乙烷的制备方法 |
| CN112608216B (zh) * | 2020-11-23 | 2022-01-21 | 浙江衢化氟化学有限公司 | 一种联产1,1-二氟乙烷和氯乙烯的方法 |
| GB202100874D0 (en) | 2021-01-22 | 2021-03-10 | Mexichem Fluor Sa De Cv | Process |
| JP7599623B1 (ja) * | 2024-01-12 | 2024-12-13 | 三菱電機株式会社 | フロン冷媒の製造方法、フロン冷媒の貯蔵方法、ヒートポンプ装置の製造方法、および二酸化炭素貯蔵システム |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2749375A (en) * | 1956-06-05 | Fluorination | ||
| US2749374A (en) | 1950-02-24 | 1956-06-05 | Dow Chemical Co | Production of methylene fluoride |
| US2744148A (en) * | 1952-02-04 | 1956-05-01 | Dow Chemical Co | Process for fluorination of haloalkanes using a hydrogen fluoride activated catalyst containing alumina, a metal fluoride and basic aluminum fluoride |
| US2749274A (en) * | 1952-05-06 | 1956-06-05 | Bristol Lab Inc | Stable aqueous procaine penicillin suspension |
| US2745886A (en) * | 1955-01-31 | 1956-05-15 | Dow Chemical Co | Process for fluorinating aliphatic halohydrocarbons with a chromium fluoride catalyst and process for preparing the catalyst |
| BE766395A (fr) * | 1971-04-28 | 1971-10-28 | Solvay | Procede de fabrication du 1,1-difluorethane, |
| JPS5233604B2 (es) * | 1973-05-08 | 1977-08-30 | ||
| US4147733A (en) * | 1978-05-22 | 1979-04-03 | The Dow Chemical Company | Fluorination of chlorinated hydrocarbons |
| US5208395A (en) * | 1992-04-06 | 1993-05-04 | Elf Atochem North America, Inc. | Manufacture of hydrofluorocarbons |
| GB9404715D0 (en) * | 1993-03-24 | 1994-04-27 | Ici Plc | Production of difluoromethane |
| EP0712826A1 (en) | 1994-11-17 | 1996-05-22 | Elf Atochem North America, Inc. | 1,1,1-Trifluoroethane synthesis using a supported lewis acid |
| FR2736050B1 (fr) | 1995-06-29 | 1997-08-01 | Atochem Elf Sa | Procede de fabrication du difluoromethane |
| FR2748022B1 (fr) * | 1996-04-29 | 1998-07-24 | Atochem Elf Sa | Procede de fabrication du difluoromethane |
| JPH10120602A (ja) * | 1996-08-06 | 1998-05-12 | Asahi Glass Co Ltd | 含水素フッ素化アルカンの製造方法 |
| JP3367861B2 (ja) * | 1997-04-15 | 2003-01-20 | セントラル硝子株式会社 | 3,3−ジクロロ−1,1,1−トリフルオロアセトンの製造方法 |
| US6080899A (en) | 1999-01-25 | 2000-06-27 | Alliedsignal Inc. | Method of producing fluorinated organic compounds |
-
2004
- 2004-04-01 US US10/816,447 patent/US7112708B2/en not_active Expired - Lifetime
-
2005
- 2005-03-31 EP EP11000069.2A patent/EP2336101B1/en not_active Expired - Lifetime
- 2005-03-31 AT AT05779894T patent/ATE556043T1/de active
- 2005-03-31 ES ES05779894T patent/ES2386898T3/es not_active Expired - Lifetime
- 2005-03-31 ES ES11000069.2T patent/ES2547073T3/es not_active Expired - Lifetime
- 2005-03-31 EP EP05779894A patent/EP1735258B1/en not_active Expired - Lifetime
- 2005-03-31 CN CNB2005800163262A patent/CN100526271C/zh not_active Expired - Fee Related
- 2005-03-31 JP JP2007506320A patent/JP4871261B2/ja not_active Expired - Fee Related
- 2005-03-31 KR KR1020067022958A patent/KR101163528B1/ko not_active Expired - Fee Related
- 2005-03-31 WO PCT/US2005/011125 patent/WO2005097716A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| KR101163528B1 (ko) | 2012-07-10 |
| CN1956940A (zh) | 2007-05-02 |
| ATE556043T1 (de) | 2012-05-15 |
| EP1735258A1 (en) | 2006-12-27 |
| EP2336101B1 (en) | 2015-07-01 |
| KR20070002080A (ko) | 2007-01-04 |
| WO2005097716A1 (en) | 2005-10-20 |
| US7112708B2 (en) | 2006-09-26 |
| EP2336101A1 (en) | 2011-06-22 |
| EP1735258B1 (en) | 2012-05-02 |
| CN100526271C (zh) | 2009-08-12 |
| US20050222472A1 (en) | 2005-10-06 |
| JP4871261B2 (ja) | 2012-02-08 |
| ES2386898T3 (es) | 2012-09-05 |
| JP2007531732A (ja) | 2007-11-08 |
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