US20200172456A1 - Composition including fluoromethane and method for producing same - Google Patents
Composition including fluoromethane and method for producing same Download PDFInfo
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- US20200172456A1 US20200172456A1 US16/784,740 US202016784740A US2020172456A1 US 20200172456 A1 US20200172456 A1 US 20200172456A1 US 202016784740 A US202016784740 A US 202016784740A US 2020172456 A1 US2020172456 A1 US 2020172456A1
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- United States
- Prior art keywords
- fluoromethane
- hydrocarbon group
- composition
- optionally substituted
- alumina catalyst
- Prior art date
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- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 title claims abstract description 113
- 239000000203 mixture Substances 0.000 title claims abstract description 35
- 238000004519 manufacturing process Methods 0.000 title abstract description 11
- 239000003054 catalyst Substances 0.000 claims abstract description 60
- 239000007789 gas Substances 0.000 claims abstract description 57
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 56
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims abstract description 26
- 239000002253 acid Substances 0.000 claims abstract description 26
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 18
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 18
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 18
- 239000000460 chlorine Substances 0.000 claims abstract description 18
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 14
- 239000011737 fluorine Substances 0.000 claims abstract description 14
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims abstract description 13
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims abstract description 9
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 6
- 150000002367 halogens Chemical class 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 5
- 239000001257 hydrogen Substances 0.000 claims abstract description 5
- 150000002431 hydrogen Chemical class 0.000 claims abstract 3
- 238000000034 method Methods 0.000 claims description 25
- 238000001312 dry etching Methods 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 description 36
- 239000007858 starting material Substances 0.000 description 21
- 238000000197 pyrolysis Methods 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 238000009835 boiling Methods 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 239000012535 impurity Substances 0.000 description 10
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 10
- VWBMDRDQJLUMMS-UHFFFAOYSA-N 4-fluoro-1-iodo-2-methylbenzene Chemical compound CC1=CC(F)=CC=C1I VWBMDRDQJLUMMS-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 8
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- -1 trimethyl Chemical group 0.000 description 7
- 239000007795 chemical reaction product Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000003682 fluorination reaction Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 0 [1*]C([2*])OC Chemical compound [1*]C([2*])OC 0.000 description 5
- 239000000356 contaminant Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 4
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 4
- 238000011109 contamination Methods 0.000 description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 4
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 4
- 229940050176 methyl chloride Drugs 0.000 description 4
- DAFIBNSJXIGBQB-UHFFFAOYSA-N perfluoroisobutene Chemical group FC(F)=C(C(F)(F)F)C(F)(F)F DAFIBNSJXIGBQB-UHFFFAOYSA-N 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 2
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 2
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 2
- PNIDBKALSVNXJB-UHFFFAOYSA-N 3,3,3-trifluoro-2-(trifluoromethyl)propanoyl fluoride Chemical compound FC(=O)C(C(F)(F)F)C(F)(F)F PNIDBKALSVNXJB-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 2
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Chemical group 0.000 description 2
- 238000011088 calibration curve Methods 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 238000010813 internal standard method Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000004445 quantitative analysis Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- VNXYDFNVQBICRO-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoro-2-methoxypropane Chemical compound COC(C(F)(F)F)C(F)(F)F VNXYDFNVQBICRO-UHFFFAOYSA-N 0.000 description 1
- NDMMKOCNFSTXRU-UHFFFAOYSA-N 1,1,2,3,3-pentafluoroprop-1-ene Chemical compound FC(F)C(F)=C(F)F NDMMKOCNFSTXRU-UHFFFAOYSA-N 0.000 description 1
- QAERDLQYXMEHEB-UHFFFAOYSA-N 1,1,3,3,3-pentafluoroprop-1-ene Chemical compound FC(F)=CC(F)(F)F QAERDLQYXMEHEB-UHFFFAOYSA-N 0.000 description 1
- FYLUVRPNPUVQOJ-UHFFFAOYSA-N CC=C.F.F.F.F.F Chemical compound CC=C.F.F.F.F.F FYLUVRPNPUVQOJ-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- 241001539176 Hime Species 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 238000001036 glow-discharge mass spectrometry Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/361—Preparation of halogenated hydrocarbons by reactions involving a decrease in the number of carbon 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
- B01J21/04—Alumina
-
- 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
- B01J6/00—Heat treatments such as Calcining; Fusing ; Pyrolysis
- B01J6/008—Pyrolysis reactions
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/02—Boron or aluminium; Oxides or hydroxides thereof
- C07C2521/04—Alumina
Definitions
- perfluoroisobutylene (CF 3 ) 2 C ⁇ CF 2 )
- perfluoroisobutylene (CF 3 ) 2 C ⁇ CF 2 )
- 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether can be obtained by reacting perfluoroisobutylene with methanol.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
An object of the present invention is to provide a composition containing fluoromethane having high purity. A method for producing fluoromethane, comprising: pyrolyzing in a gas phase a fluorine-containing methyl ether represented by Formula (1):
- wherein R1 and R2 are the same or different, and each represents an optionally substituted linear or branched monovalent aliphatic hydrocarbon group, an optionally substituted monovalent aromatic hydrocarbon group, an optionally substituted monovalent cyclic aliphatic hydrocarbon group, hydrogen, or halogen, in the presence of an alumina catalyst to thereby obtain a mixed gas containing fluoromethane and acid fluoride, wherein: the alumina catalyst contains chlorine in an amount of 1.0 wt % or less.
Description
- The present invention relates to a composition comprising fluoromethane useful as a dry etching gas, and a method for producing the composition.
- Hydrofluorocarbons are useful as etching gases for the microfabrication of semiconductors, liquid crystals, and the like. In particular, fluoromethane (CH3F) is drawing attention as an etching gas for forming state-of-the-art microstructures.
- A known method for producing fluoromethane is, for example, a method in which a mixed gas containing fluoromethane and acid fluoride is obtained by pyrolyzing a starting compound in a gas phase in the presence of an alumina catalyst (Patent Document 1).
- Patent Document 1: JP2014-114277A
- An object of the present invention is to provide a composition containing fluoromethane having high purity.
- The inventors of the present invention conducted extensive research to attain the above object. It is known that an alumina catalyst is treated with hydrochloric acid in some cases to increase the reaction activity. As a result of the research, the present inventors found contamination of a small amount of methane, ethane, propane, methyl chloride, and the like in the reaction product due to the hydrochloric acid treatment. Of these contaminants, it is difficult to remove methyl chloride, even if the amount thereof is only several ppm. Regarding this problem, the present inventors discovered that the contamination of impurities in the final product may be prevented by using an alumina catalyst untreated with hydrochloric acid. The present invention has been completed upon further trial and error based on these findings, and encompasses the following items.
- A method for producing fluoromethane, comprising:
- pyrolyzing in a gas phase a fluorine-containing methyl ether represented by Formula (1):
- wherein R1 and R2 are the same or different, and each represents an optionally substituted linear or branched monovalent aliphatic hydrocarbon group, an optionally substituted monovalent aromatic hydrocarbon group, an optionally substituted monovalent cyclic aliphatic hydrocarbon group, hydrogen, or halogen,
- in the presence of an alumina catalyst to thereby obtain a mixed gas containing fluoromethane and acid fluoride,
- wherein:
- the alumina catalyst contains chlorine in an amount of 1.0 wt % or less.
- The method according to Item 1, wherein the catalyst is a γ-alumina catalyst.
- A composition comprising fluoromethane obtainable by the method of Item 1 or 2.
- A composition comprising fluoromethane in an amount of 99.999 mol % or more based on the total weight of the composition.
- The composition according to Item 3 or 4, wherein the composition is used as a dry etching gas.
- An alumina catalyst containing chlorine in an amount of 1.0 wt % or less, for use in a method for producing fluoromethane,
- the method comprising pyrolyzing a starting compound in a gas phase in the presence of a catalyst to thereby obtain a mixed gas containing fluoromethane and acid fluoride.
- The alumina catalyst according to Item 6, wherein the alumina catalyst is a γ-alumina catalyst.
- The present invention is capable of providing a composition containing fluoromethane having high purity.
- The method for producing fluoromethane according to the present invention comprises the step of pyrolyzing a starting compound in a gas phase in the presence of an alumina catalyst to thereby obtain a mixed gas containing fluoromethane and acid fluoride, wherein the alumina catalyst contains chlorine in an amount of 1.0 wt % or less.
- The reaction of performing pyrolysis in a gas phase to thereby obtain a mixed gas containing fluoromethane and acid fluoride has already been known, as disclosed, for example, in JP2014-114277A and the like.
- The present invention uses a fluorine-containing methyl ether represented by Formula (1) as a starting compound.
- (wherein R1 and R2 are the same or different, and each represents an optionally substituted linear or branched monovalent aliphatic hydrocarbon group, an optionally substituted monovalent aromatic hydrocarbon group, an optionally substituted monovalent cyclic aliphatic hydrocarbon group, hydrogen, or halogen).
- The method for producing fluorine-containing methyl ether to be used as a starting compound is not particularly limited, and compounds obtained by any methods may be used.
- In Formula (1) above, preferably, R1 and R2 are the same or different, and each represents an optionally substituted C1-30 linear or branched monovalent aliphatic hydrocarbon group, an optionally substituted C6-12 monovalent aromatic hydrocarbon group, or an optionally substituted C6-12 monovalent cyclic aliphatic hydrocarbon group. More preferably, R1 and R2 are the same or different, and each represents an optionally substituted C1-10 linear or branched monovalent aliphatic hydrocarbon group, an optionally substituted C6 10 monovalent aromatic hydrocarbon group, or an optionally substituted C6-10 monovalent cyclic aliphatic hydrocarbon group.
- Examples of the above C1-10 linear or branched monovalent aliphatic hydrocarbon group include, but are not particularly limited to, C1 10 alkyl group and the like.
- More specifically, examples of C1-10 alkyl include methyl, ethyl, trimethyl, propyl, 2-methylethyl, hexyl, octyl, and the like.
- The C1 10 alkyl is preferably C1 6 alkyl, more preferably C1-4 alkyl, further preferably C1-3 alkyl.
- Examples of C6-10 monovalent aromatic hydrocarbon group include, but are not particularly limited to, phenyl, methyl phenyl, ethyl phenyl, and the like.
- Examples of C6-10 monovalent cyclic aliphatic hydrocarbon group include, but are not particularly limited to, cyclohexyl, methyl cyclohexyl, ethyl cyclohexyl, and the like.
- In the above formula, at least one hydrogen atom of the monovalent aliphatic hydrocarbon group, monovalent aromatic hydrocarbon group, or monovalent cyclic aliphatic hydrocarbon group may be replaced by at least one heteroatom selected from the group consisting of fluorine, chlorine, and bromine; or all hydrogen atoms may be replaced.
- In the above formula, the halogen is preferably fluorine, chlorine, or bromine; and more preferably fluorine.
- Examples of specific compounds that can be used as starting compounds include, but are not limited to, 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether and the like.
- In particular, perfluoroisobutylene ((CF3)2C═CF2) , which is obtained as a by-product when hexafluoropropene used as a starting compound of fluororesin is produced, has hitherto been discarded as waste; however, 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether can be obtained by reacting perfluoroisobutylene with methanol. Use of the thus-obtained 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether as a starting compound in the present invention allows for effective utilization of waste, and enables the desired product to be produced inexpensively using the low-cost starting compound. In the present invention, the phrase stating that 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether used as a starting compound is “obtained by reacting perfluoroisobutylene and methanol” is limited to the meaning that the 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether is obtained by said reaction, and is not obtained by other methods. The method for obtaining 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether by reacting perfluoroisobutylene and methanol is a known method, and may be conducted in accordance with known reaction conditions. For example, the reaction may be performed in accordance with the method disclosed in JP2001-506261A.
- Although the method is not particularly limited, fluoromethane and 3,3,3-trifluoro-2-(trifluoromethyl)propanoyl fluoride may be obtained by, for example, pyrolyzing 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether, which is a starting compound. By rectifying this mixed gas, a composition containing fluoromethane at high purity may be obtained. The present inventors clarified that this composition contains a small amount of HFC-1225zc as a contaminant.
- An alumina catalyst containing a small amount of chlorine is used as a catalyst. Alumina catalysts include those containing chlorine as an impurity, or those treated with hydrochloric acid to improve the reaction activity. Therefore, these alumina catalysts contain chlorine as a contaminant. If the pyrolysis reaction of the present invention is performed using an alumina catalyst thus containing chlorine, the reaction product contains a small amount of methane, ethane, propane, methyl chloride, and the like as contaminants. In particular, the present inventors confirmed difficulties in removing even several ppm of methyl chloride. Therefore, the present invention is characterized by using an alumina catalyst containing a small amount of chlorine. Using such an alumina catalyst prevents the contamination of impurities in the reaction product.
- In other words, the present invention uses an alumina catalyst containing chlorine in an amount of 1.0 wt % or less, preferably 0.5 wt % or less, more preferably 0.1 wt % or less; further preferably, the present invention uses an alumina catalyst with a chlorine content of no more than the detection limit.
- In the present invention, the content of contaminants in the alumina catalyst is measured as follows using glow-discharge mass spectrometry. The surface of an alumina catalyst sample is sputtered by glow discharge under an Ar atmosphere, and the emitted neutral particles are ionized by the collision with Ar and electrons in the plasma; and the ions are measured by a high-resolution mass spectrometer.
- In the present invention, the pore volume may be measured by a commonly used gas adsorption method using a device from Nippon-bel.co.jp, or a similar device.
- α-alumina and activated alumina and the like may be used as an alumina catalyst. Examples of activated alumina include ρ-alumina, χ-alumina, κ-alumina, η-alumina, pseudo-γ-alumina, γ-alumina, δ-alumina and θ-alumina. Of these, γ-alumina and η-alumina are preferable, and γ-alumina is particularly preferable. Further, silica alumina (SiO2/Al2O3), a composite oxide, may also be used as a catalyst. The proportion of silica SiO2 in silica alumina is preferably 20 to 90 wt %, and more preferably 50 to 80 wt %.
- The larger the pore volume of the catalyst, the higher the activity. The pore volume of the catalyst is preferably 0.4 ml/g or more, and particularly preferably 0.6 ml/g or more.
- Further, the catalyst may have deposited thereon fluorides of alkali metals and alkaline earth metals, such as KF, NaF, and MgF2.
- In the present invention, fluorinated alumina catalysts may also be used. There is no particular limitation on the method for obtaining the above-mentioned fluorinated alumina catalysts. For example, the fluorinated alumina catalysts can be obtained by bringing the above-described alumina catalysts into contact with anhydrous hydrogen fluoride or fluorocarbon while heating to allow a fluorination reaction to proceed. The method for bringing the alumina catalysts into contact with hydrogen fluoride is not particularly limited, and may be a continuous flow method in which hydrogen fluoride is allowed to flow through a reaction tube containing the catalyst, or a batch method in which hydrogen fluoride or fluorocarbon is enclosed in a container containing the catalyst. In particular, the flow method is preferable in terms of a short treatment time.
- The fluorocarbon is preferably one with a large number of fluorine atoms and a small number of carbon atoms. Examples of fluorocarbon include trifluoromethane, difluorochloromethane, octafluoroethane, and the like.
- The degree of fluorination of such an alumina catalyst is not particularly limited; those having a fluorine content of about 5 to 50 wt % based on the total weight of fluorinated alumina catalyst are preferably used.
- The temperature of the fluorination treatment for such an alumina catalyst is preferably higher than that of the below-described pyrolysis reaction; and is, for example, preferably about 150 to 500° C., more preferably about 200° C. to 400° C., further preferably about 250° C. to 350° C. An excessively low temperature in the fluorination treatment decreases the effect of the catalyst because of insufficient fluorination, whereas an excessively high temperature in the fluorination treatment additionally requires a heat-resistant material; thus, it is not practical.
- The pyrolysis reaction of fluorine-containing methyl ether may be advanced by bringing the fluorine-containing methyl ether into contact with the above-described catalyst in a gas phase in the presence of the catalyst. There is no particular limitation on the specific method: an example is a method in which the catalyst is placed in a tubular flow reactor, and fluorine-containing methyl ether used as a starting material is introduced to the reactor and brought into contact with the catalyst in a gas phase.
- If the temperature of the pyrolysis reaction is excessively low, the conversion of the starting material tends to decrease. If the temperature of the pyrolysis reaction is excessively high, impurities tend to increase. Thus, the temperature of the pyrolysis reaction is preferably about 100° C. to 400° C., further preferably about 100° C. to 300° C., particularly preferably about 100° C. to 250° C.
- An excessively low pressure in the reactor tube during the pyrolysis reaction complicates the operation because of the possible contamination of air etc., whereas an excessively high pressure in the reactor tube during the pyrolysis reaction requires that the pressure resistance of the equipment be considered, and increases the possibility of leakage. Considering these points, the pressure in the reactor tube during the pyrolysis reaction is preferably about 0.05 to 1 MPa, more preferably about 0.1 to 0.5 MPa, and particularly preferably, in terms of reaction operation, about atmospheric pressure (about 0.1 MPa).
- There is no particular limitation on the contact time for causing the reaction. The contact time represented by W/F (g·sec/cc), i.e., the ratio of the amount of the catalyst W (g) relative to the flow rate F (the flow rate at 0° C. and 1 atm (about 0.1 MPa): cc/sec) of the starting material gas, i.e., fluorine-containing methyl ether that is supplied to the reactor, is preferably about 1 to 100 g·sec/cc, more preferably about 1 to 50 g·sec/cc, and even more preferably about 5 to 30 g·sec/cc. If the contact time is excessively long, it takes a long time to obtain the product. Thus, to increase the amount of production, it is preferred that the contact time be shortened. However, if the contact time is excessively short, the conversion tends to decrease. Thus, the contact time may be selected so that the highest productivity is obtained in terms of the conversion of the starting material and the selectivity of the desired product, according to the type of catalyst to be used, the amount of the catalyst, the reaction conditions, and the like.
- In general, it is desirable to conduct the reaction by selecting the contact time so that the conversion becomes 100% , according to the type of catalyst to be used, the amount of the catalyst, the reaction conditions, and the like.
- As a result of a pyrolysis reaction, a mixed gas containing fluoromethane and acid fluoride is obtained. The mixed gas contains, in addition the desired product, i.e., fluoromethane (boiling point: −79° C.), acid fluoride that is simultaneously produced by the pyrolysis. The mixed gas may further contain at least one member of starting compound, by-products, and impurities. Although it varies depending on the starting compound, examples of by-products include propene (boiling point: −47.7° C.), propene pentafluoride (boiling point: −21.1° C.), propane (boiling point: −1.4° C.), and the like.
- By rectifying the mixed gas containing fluoromethane and acid fluoride obtained by the above pyrolysis reaction, it is possible to obtain a composition containing fluoromethane at high purity.
- The method for separating the fluoromethane and the acid fluoride contained in the resulting product is not particularly limited; for example, by cooling the gas produced by the pyrolysis reaction, it is possible to separate it into a gas component and a liquid component, the gas component containing a low-boiling-point component that contains fluoromethane (boiling point: −79° C.) as a main component, and the liquid component containing a high-boiling-point component that contains acid fluoride as a main component and may further contain unreacted starting materials. In this case, although the cooling temperature is not particularly limited, for example, the temperature is preferably as low as possible so that the fluoromethane will not be condensed. For example, the gas may be cooled to a temperature at which a pressure less than the saturated vapor pressure of fluoromethane may be maintained in an enclosed space.
- With this method, it is possible to separate a component containing fluoromethane as a gas component. The gas component may contain propene (boiling point of −47.7° C.), pentafluoropropene (boiling point of −21.1° C.), propane (boiling point of −1.4° C.), and the like, as impurities. However, these impurities can be easily separated by distillation since fluoromethane and these impurities have very different boiling points.
- In addition, when the high-boiling-point component, which is obtained as a liquid component and contains acid fluoride as a main component, contains unreacted starting materials and the like, the unreacted starting materials and the like can be easily separated by distillation.
- Further, to selectively obtain fluoromethane, the product obtained after the pyrolysis reaction may be brought into contact with water, an aqueous alkaline solution, or the like to dissolve acid fluoride in an aqueous phase, thereby removing the acid fluoride. This enables selective collection of fluoromethane.
- In the above process, an alcohol may be used instead of water or an aqueous alkaline solution. Inexpensive alcohols are preferable in terms of cost. Examples of usable alcohols include methanol, ethanol, propanol, and the like. Of these, methanol is particularly preferable. Bringing the product into contact with an alcohol to produce an ester makes combustion treatment easier.
- Further, by subjecting the mixed gas directly to the rectification, it is possible to obtain a composition containing fluoromethane at high purity. It is therefore not necessary to remove the acid fluoride before the purification by fractionation operations or washing with water or alcohol, and the fluoromethane can be easily separated from the acid fluoride.
- The boiling point of acid fluoride is generally equal to or higher than room temperature; for example, the boiling point of 3,3,3-trifluoro-2-(trifluoromethyl)propanoyl fluoride is 32° C. Thus, the boiling point of acid fluoride is significantly higher than that of fluoromethane (boiling point: −79° C.). In the mixed gas, fluoromethane and acid fluoride are present at a molar ratio of 1:1. When the mixed gas is directly placed in an environment at around room temperature, acid fluoride is expected to be condensed. However, the present inventors unexpectedly found a phenomenon in which an interaction occurred between these two components, and the mixed gas as a whole acted as a gas that was not condensed, even at around room temperature (under predetermined pressure conditions). By taking advantage of these findings in the present invention, the mixed gas can be directly subjected to a rectification operation to efficiently separate fluoromethane.
- Preferably, the mixed gas obtained in the pyrolysis reaction is supplied to a rectification column. The supply of the mixed gas is preferably conducted at a pressure exceeding atmospheric pressure. This facilitates the transfer of the mixed gas to the rectification column. The pressure during transfer is more preferably 0.2 MPa to 0.15 MPa. At a pressure within this range, the mixed gas can be effectively supplied to the rectification column, while avoiding the condensation of the mixed gas.
- There is no particular limitation on the rectification. In general, two rectification columns are provided, and low-boiling-point components, such as methane or ethylene, are extracted from the top of a first rectification column. The remaining components containing fluoromethane and acid fluoride are obtained from the bottom of the column, and further supplied to a second rectification column. Then, fluoromethane can be extracted from the top of the column. In this method, the purity of the fluoromethane finally obtained from the top of the second rectification column is 99.999 mol % or more.
- The composition of the present invention is a composition that can be produced by the production method of the present invention, and is a composition containing 99.999 mol % or more of fluoromethane based on the total weight of the composition.
- In the above method, the weight-based proportions of the respective components based on the total weight of the composition are determined by gas chromatographic analysis (GC). Specifically, the proportions are determined as follows.
- A quantitative analysis is performed using a general internal standard method to determine the concentrations. Difluoro methane (HFC-32) and benzotrifluoride are used as internal standard substances respectively for a low-boiling-point compound and a high-boiling-point compound. Several kinds of standard samples containing known contents (molar ratios) of the internal standard substance and the test sample are analyzed, and a calibration curve of molar ratio versus peak area ratio is plotted. An internal standard substance of a known amount is added to a sample whose fluoromethane content is unknown, and the peak area ratio on the gas chromatogram is measured, thereby calculating the fluoromethane content from the relative mol sensitivity.
- The present invention is described in more detail below with reference to Examples.
- 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether (OIME) in a gas state was flowed into a reactor filled with a γ-alumina catalyst A free of chlorine heated to 150° C., and pyrolyzed. The conversion of OIME was 84%.
- The composition of the collected reaction product was as follows: 41.6 mol % of CH3F, 0.015% of HFO-1225zc (1,1,3,3,3-pentafluoro propene), 0.022 mol % of HFC-236fa (1,1,1,3,3,3-hexafluoro propane), 16.4 mol % of OIME, 41.7 mol % of acid fluoride, 0.21 mol % of HIME (1,1,1,3,3,3-hexafluoro-2-methoxy propane). The rest was other components. Methyl chloride was not detected.
- 1,1,3,3,3-pentafluoro-2-trifluoromethylpropyl methyl ether (OIME) in a gas state was flowed into a reactor filled with a γ-alumina catalyst B free of chlorine heated to 150° C., and pyrolyzed. The conversion of OIME was 92%.
- The composition of the collected reaction product was as follows: 0.002 mol % of methane, 0.0036 mol % of ethylene, 46.17 mol % of CH3F, 0.0092 mol % of propylene, 7.58 mol % of OIME, 46.17 mol % of acid fluoride, and 0.0615 mol % of other components. Methyl chloride was not detected.
- These substances were transferred to the rectification column to be purified. Impurities were not detected after the rectification, and the purity of CH3F was determined to be 99.999 mol % or more.
- In the present Examples and Comparative Examples, the mol concentrations of the respective components based on the total amount of the composition were determined as follows by gas chromatographic analysis (GC).
- Quantitative analysis was performed using a general internal standard method to determine the concentrations. Difluoro methane (HFC-32) and benzotrifluoride were respectively used as internal standard substances for a low-boiling-point compound and a high-boiling-point compound. Several kinds of standard samples containing known contents (molar ratios) of the internal standard substance and the test sample were analyzed, and a calibration curve of molar ratio versus peak area ratio was plotted. An internal standard substance of a known amount was added to a sample whose fluoromethane content was unknown, and the peak area ratio on the gas chromatogram was measured, thereby calculating the fluoromethane content from the relative mol sensitivity.
- Under the same reaction conditions as those of Example 2, OIME in a gas state was flowed into a reactor filled with a γ-alumina catalyst C containing 1.4 wt % of chlorine, and pyrolyzed. The conversion of OIME was 91%. The composition of the collected reaction product was as follows: 0.001 mol % of methane, 0.0002 mol % of ethylene, 46.49 mol % of CH3F, 0.001 mol % of propylene, 0.004 mol % of methyl chloride, 8.6 mol % of OIME, 44.6 mol % of acid fluoride. The rest was other substances.
- The purity after the rectification was 99.9983%, and 0.0013 mol % of methyl chloride and 0.0004 mol % of propylene were contained as impurities.
Claims (8)
1-2. (canceled)
3. A composition comprising fluoromethane obtainable by a method comprising:
pyrolyzing in a gas phase a fluorine-containing methyl ether represented by Formula (1):
wherein R1 and R2 are the same or different, and each represents an optionally substituted linear or branched monovalent aliphatic hydrocarbon group, an optionally substituted monovalent aromatic hydrocarbon group, an optionally substituted monovalent cyclic aliphatic hydrocarbon group, hydrogen, or halogen,
in the presence of an alumina catalyst to thereby obtain a mixed gas containing fluoromethane and acid fluoride,
wherein:
the alumina catalyst contains chlorine in an amount of 1.0 wt % or less.
4. A composition comprising fluoromethane in an amount of 99.999 mol % or more based on the total weight of the composition.
5. The composition according to claim 3 , wherein the composition is used as a dry etching gas.
6-7. (canceled)
8. A composition comprising fluoromethane obtainable by a method comprising:
pyrolyzing in a gas phase a fluorine-containing methyl ether represented by Formula (1):
wherein R1 and R2 are the same or different, and each represents an optionally substituted linear or branched monovalent aliphatic hydrocarbon group, an optionally substituted monovalent aromatic hydrocarbon group, an optionally substituted monovalent cyclic aliphatic hydrocarbon group, hydrogen, or halogen,
in the presence of a γ-alumina catalyst to thereby obtain a mixed gas containing fluoromethane and acid fluoride,
wherein:
the γ-alumina catalyst contains chlorine in an amount of 1.0 wt % or less.
9. The composition according to claim 8 , wherein the composition is used as a dry etching gas.
10. The composition according to claim 4 , wherein the composition is used as a dry etching gas.
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PCT/JP2016/066535 WO2016195055A1 (en) | 2015-06-03 | 2016-06-03 | Composition including fluoromethane and method for producing same |
US201715577963A | 2017-11-29 | 2017-11-29 | |
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