GB1561535A - Process for producing fluoroalkanes - Google Patents
Process for producing fluoroalkanes Download PDFInfo
- Publication number
- GB1561535A GB1561535A GB43403/76A GB4340376A GB1561535A GB 1561535 A GB1561535 A GB 1561535A GB 43403/76 A GB43403/76 A GB 43403/76A GB 4340376 A GB4340376 A GB 4340376A GB 1561535 A GB1561535 A GB 1561535A
- Authority
- GB
- United Kingdom
- Prior art keywords
- process according
- catalyst
- aluminium oxide
- impregnated
- bismuth
- 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
- 238000000034 method Methods 0.000 title claims description 33
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 50
- 239000003054 catalyst Substances 0.000 claims description 38
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 16
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 14
- 150000001621 bismuth Chemical class 0.000 claims description 13
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 10
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 239000004215 Carbon black (E152) Substances 0.000 claims description 9
- 150000002696 manganese Chemical class 0.000 claims description 9
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical group CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 claims description 7
- 229910052797 bismuth Inorganic materials 0.000 claims description 7
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 239000011572 manganese Substances 0.000 claims description 3
- 229910017604 nitric acid Inorganic materials 0.000 claims description 3
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 150000003839 salts Chemical group 0.000 claims description 2
- 239000001117 sulphuric acid Substances 0.000 claims description 2
- 235000011149 sulphuric acid Nutrition 0.000 claims description 2
- -1 bismuth salt Chemical class 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminium flouride Chemical compound F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 6
- 229940051271 1,1-difluoroethane Drugs 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000012266 salt solution Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 3
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000008246 gaseous mixture Substances 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- WAEMQWOKJMHJLA-UHFFFAOYSA-N Manganese(2+) Chemical compound [Mn+2] WAEMQWOKJMHJLA-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- JVWLUVNSQYXYBE-UHFFFAOYSA-N Ribitol Natural products OCC(C)C(O)C(O)CO JVWLUVNSQYXYBE-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001399 aluminium compounds Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 229940077746 antacid containing aluminium compound Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001622 bismuth compounds Chemical class 0.000 description 1
- BRCWHGIUHLWZBK-UHFFFAOYSA-K bismuth;trifluoride Chemical compound F[Bi](F)F BRCWHGIUHLWZBK-UHFFFAOYSA-K 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000010724 circulating oil Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- HEBKCHPVOIAQTA-ZXFHETKHSA-N ribitol Chemical compound OC[C@H](O)[C@H](O)[C@H](O)CO HEBKCHPVOIAQTA-ZXFHETKHSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- IAHFWCOBPZCAEA-UHFFFAOYSA-N succinonitrile Chemical compound N#CCCC#N IAHFWCOBPZCAEA-UHFFFAOYSA-N 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- B01J27/12—Fluorides
-
- 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
- B01J23/32—Manganese, technetium or rhenium
- B01J23/34—Manganese
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/07—Preparation of halogenated hydrocarbons by addition of hydrogen halides
- C07C17/08—Preparation of halogenated hydrocarbons by addition of hydrogen halides to unsaturated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752547182 DE2547182A1 (de) | 1975-10-22 | 1975-10-22 | Verfahren zur herstellung von 1,1-difluoraethan |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1561535A true GB1561535A (en) | 1980-02-20 |
Family
ID=5959720
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB43403/76A Expired GB1561535A (en) | 1975-10-22 | 1976-10-19 | Process for producing fluoroalkanes |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4138439A (cg-RX-API-DMAC7.html) |
| JP (1) | JPS5251304A (cg-RX-API-DMAC7.html) |
| BE (1) | BE847456A (cg-RX-API-DMAC7.html) |
| CA (1) | CA1067916A (cg-RX-API-DMAC7.html) |
| CH (1) | CH622234A5 (cg-RX-API-DMAC7.html) |
| DE (1) | DE2547182A1 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2328681A1 (cg-RX-API-DMAC7.html) |
| GB (1) | GB1561535A (cg-RX-API-DMAC7.html) |
| IT (1) | IT1069585B (cg-RX-API-DMAC7.html) |
| NL (1) | NL7611664A (cg-RX-API-DMAC7.html) |
| SE (1) | SE414763B (cg-RX-API-DMAC7.html) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4798818A (en) * | 1987-11-27 | 1989-01-17 | Dow Corning Corporation | Catalyst composition and process for its preparation |
| DE3936024A1 (de) * | 1989-10-28 | 1991-05-02 | Bayer Ag | Verfahren zum halogen-fluor-austausch in organischen verbindungen und katalysatoren hierzu |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2471525A (en) * | 1947-12-19 | 1949-05-31 | Phillips Petroleum Co | Reaction of an acetylene with hf to produce vinyl fluoride and/or difluoroethane andhomologues thereof |
| NL301860A (cg-RX-API-DMAC7.html) * | 1962-12-28 | |||
| US3395187A (en) * | 1965-05-03 | 1968-07-30 | Du Pont | Process for preparing vinyl fluoride and 1, 1-difluoroethane |
| US3904701A (en) * | 1969-01-03 | 1975-09-09 | Dynamit Nobel Ag | Process for the catalytic hydrofluorination of halogenated hydrocarbons |
| DE2000200C3 (de) * | 1970-01-03 | 1980-01-24 | Dynamit Nobel Ag, 5210 Troisdorf | Verfahren zur Herstellung von fluorierten aliphatischen Kohlenwasserstoffen mit zwei und mehr C-Atomen oder von fluorierten cycloaliphatischen Kohlenwasserstoffen |
| JPS5016767B1 (cg-RX-API-DMAC7.html) * | 1969-12-24 | 1975-06-16 | ||
| US3720722A (en) * | 1971-02-18 | 1973-03-13 | Daikin Ind Ltd | Novel aluminum fluoride catalyst and process for hydrofluorinating acetylene using same |
| BE787410A (fr) * | 1971-08-10 | 1973-02-12 | Bayer Ag | Procede de preparation du 1,1-difluorethane |
-
1975
- 1975-10-22 DE DE19752547182 patent/DE2547182A1/de not_active Withdrawn
-
1976
- 1976-10-18 CA CA263,558A patent/CA1067916A/en not_active Expired
- 1976-10-19 GB GB43403/76A patent/GB1561535A/en not_active Expired
- 1976-10-20 IT IT51822/76A patent/IT1069585B/it active
- 1976-10-20 BE BE171647A patent/BE847456A/xx unknown
- 1976-10-20 US US05/734,212 patent/US4138439A/en not_active Expired - Lifetime
- 1976-10-21 FR FR7631720A patent/FR2328681A1/fr active Granted
- 1976-10-21 CH CH1331076A patent/CH622234A5/de not_active IP Right Cessation
- 1976-10-21 SE SE7611683A patent/SE414763B/xx unknown
- 1976-10-21 NL NL7611664A patent/NL7611664A/xx not_active Application Discontinuation
- 1976-10-22 JP JP51127126A patent/JPS5251304A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5251304A (en) | 1977-04-25 |
| DE2547182A1 (de) | 1977-05-05 |
| BE847456A (fr) | 1977-02-14 |
| FR2328681A1 (fr) | 1977-05-20 |
| NL7611664A (nl) | 1977-04-26 |
| US4138439A (en) | 1979-02-06 |
| SE414763B (sv) | 1980-08-18 |
| CA1067916A (en) | 1979-12-11 |
| IT1069585B (it) | 1985-03-25 |
| FR2328681B1 (cg-RX-API-DMAC7.html) | 1982-11-12 |
| SE7611683L (sv) | 1977-04-23 |
| CH622234A5 (cg-RX-API-DMAC7.html) | 1981-03-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4600571A (en) | Catalysts and their use in ammonia production | |
| JP2557936B2 (ja) | 触媒の存在下でのフッ化水素化による１，１，１−トリフルオロ−２，２−ジクロロエタンの製法 | |
| AU592431B2 (en) | Improved silver catalyst | |
| US3803241A (en) | Process for the catalytic fluorination of saturated and unsaturated halogenated hydrocarbons | |
| US3862995A (en) | Manufacture of 1,1-difluoroethane | |
| US3904701A (en) | Process for the catalytic hydrofluorination of halogenated hydrocarbons | |
| JPH0348632A (ja) | １，１，１，２―テトラフルオロエタンの製造法 | |
| US4181629A (en) | Catalyst for the oxidation of methanol to formaldehyde and a method of preparing the catalyst | |
| JPH1147601A (ja) | 触媒ハロゲン化有機化合物のフッ素化方法 | |
| JP2537734B2 (ja) | 硫黄化合物含有ガスを処理するための触媒及び方法 | |
| JP3220525B2 (ja) | ジアルキルカーボネートの製造方法 | |
| US5345014A (en) | Process for preparing pentafluoroethane by dismutation of tetrafluorochloroethane | |
| JPS5821900B2 (ja) | ヘキサフルオルプロパノン −２ ノセイゾウホウ | |
| US6436362B1 (en) | Process for preparing aluminum fluoride | |
| CA1067916A (en) | Process for the production of 1,1-difluoro ethane | |
| EP0559926B1 (en) | Method for preparing a catalyst for conversion of methane to higher hydrocarbons and for dehydrogenating hydrocarbons | |
| JPH0531533B2 (cg-RX-API-DMAC7.html) | ||
| US4178316A (en) | Method of preparing 1,1-difluoroethylene from acetylene | |
| US3965038A (en) | Regeneration of bismuth containing catalyst used in the hydrofluorination of halogenated hydrocarbons | |
| JPS61221139A (ja) | ２，２，２‐トリフルオロエタノールの製造法 | |
| US7098166B2 (en) | Catalyst for preparing fluorine-containing alcohol compound and a process for preparation of fluorine-containing alcohol compound | |
| DE1900241A1 (de) | Verfahren zur katalytischen Hydrofluorierung von halogenierten Kohlenwasserstoffen | |
| JP3300120B2 (ja) | １，１，１−トリフルオロ−２−クロロエタンの製造方法 | |
| JP2000070713A (ja) | ハロゲン化有機化合物のフッ素化用触媒 | |
| DE2000200C3 (de) | Verfahren zur Herstellung von fluorierten aliphatischen Kohlenwasserstoffen mit zwei und mehr C-Atomen oder von fluorierten cycloaliphatischen Kohlenwasserstoffen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |