SU477575A3 - Способ получени низших перфторалканов и циклических перфторолефинов - Google Patents
Способ получени низших перфторалканов и циклических перфторолефиновInfo
- Publication number
- SU477575A3 SU477575A3 SU1677039A SU1677039A SU477575A3 SU 477575 A3 SU477575 A3 SU 477575A3 SU 1677039 A SU1677039 A SU 1677039A SU 1677039 A SU1677039 A SU 1677039A SU 477575 A3 SU477575 A3 SU 477575A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- pyrolysis
- pressure
- temperature
- vessel
- cyclic
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 7
- 125000004122 cyclic group Chemical group 0.000 title claims description 5
- 238000000197 pyrolysis Methods 0.000 claims description 12
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 4
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 4
- 239000011261 inert gas Substances 0.000 claims description 3
- 238000002955 isolation Methods 0.000 claims description 3
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 0.000 claims 1
- 150000002832 nitroso derivatives Chemical class 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 239000000047 product Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000004821 distillation Methods 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical compound NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- -1 polytetrafluoroethylene fluoride Polymers 0.000 description 5
- 238000007792 addition Methods 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical class FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 4
- 239000004810 polytetrafluoroethylene Substances 0.000 description 4
- RMHCWMIZBMGHKV-UHFFFAOYSA-N 1,1,2,3,3,4,4,5,5,6,6,6-dodecafluorohex-1-ene Chemical compound FC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F RMHCWMIZBMGHKV-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- ZVJOQYFQSQJDDX-UHFFFAOYSA-N 1,1,2,3,3,4,4,4-octafluorobut-1-ene Chemical compound FC(F)=C(F)C(F)(F)C(F)(F)F ZVJOQYFQSQJDDX-UHFFFAOYSA-N 0.000 description 2
- QVHWOZCZUNPZPW-UHFFFAOYSA-N 1,2,3,3,4,4-hexafluorocyclobutene Chemical compound FC1=C(F)C(F)(F)C1(F)F QVHWOZCZUNPZPW-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000004992 fission Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- UVWPNDVAQBNQBG-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-icosafluorononane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F UVWPNDVAQBNQBG-UHFFFAOYSA-N 0.000 description 1
- YCBPKOZNGFQMPB-UHFFFAOYSA-N 1,1,2,3,3,4,4,5,5,6,6,7,7,8,8,8-hexadecafluorooct-1-ene Chemical compound FC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YCBPKOZNGFQMPB-UHFFFAOYSA-N 0.000 description 1
- YBMDPYAEZDJWNY-UHFFFAOYSA-N 1,2,3,3,4,4,5,5-octafluorocyclopentene Chemical class FC1=C(F)C(F)(F)C(F)(F)C1(F)F YBMDPYAEZDJWNY-UHFFFAOYSA-N 0.000 description 1
- NYEZNHLGLOQHEE-UHFFFAOYSA-N 1,2,3,4,5,5,6,6-octafluorocyclohexa-1,3-diene Chemical compound FC1=C(F)C(F)(F)C(F)(F)C(F)=C1F NYEZNHLGLOQHEE-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 230000005526 G1 to G0 transition Effects 0.000 description 1
- 241000208202 Linaceae Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 150000001925 cycloalkenes Chemical class 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 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
- 239000012263 liquid product Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003822 preparative gas chromatography Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011265 semifinished product Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 229910052815 sulfur oxide Inorganic materials 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C07C17/367—Preparation of halogenated hydrocarbons by reactions involving a decrease in the number of carbon atoms by depolymerisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19702031047 DE2031047C3 (de) | 1970-06-24 | Verfahren zur Herstellung cyclischer Perfluorolefine mit 4 bis 6 Ringgliedern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU477575A3 true SU477575A3 (ru) | 1975-07-15 |
Family
ID=5774740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1677039A SU477575A3 (ru) | 1970-06-24 | 1971-06-23 | Способ получени низших перфторалканов и циклических перфторолефинов |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3816552A (enExample) |
| BE (1) | BE768850A (enExample) |
| CA (1) | CA943973A (enExample) |
| CH (1) | CH565723A5 (enExample) |
| FR (1) | FR2096789B1 (enExample) |
| GB (1) | GB1338425A (enExample) |
| NL (1) | NL7108425A (enExample) |
| SU (1) | SU477575A3 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5220082A (en) * | 1990-10-11 | 1993-06-15 | E. I. Du Pont De Nemours And Company | Process for production of polyfluoroolefins |
| CA2398476C (en) | 2000-02-10 | 2009-11-24 | South African Nuclear Energy Corporation Limited | Treatment of fluorocarbon feedstocks |
| PL201719B1 (pl) * | 2000-02-10 | 2009-05-29 | 3 M Innovative Properties Comp | Sposób obróbki surowca fluorowęglowodorowego |
| US7003035B2 (en) * | 2002-01-25 | 2006-02-21 | Microsoft Corporation | Video coding methods and apparatuses |
| US6919015B2 (en) * | 2002-12-16 | 2005-07-19 | 3M Innovative Properties Company | Process for manufacturing fluoroolefins |
| 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 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2664449A (en) * | 1947-01-06 | 1953-12-29 | William T Miller | Pyrolysis of trifluorochloroethylene polymers |
-
1971
- 1971-06-08 CA CA115,067A patent/CA943973A/en not_active Expired
- 1971-06-18 NL NL7108425A patent/NL7108425A/xx unknown
- 1971-06-21 CH CH903671A patent/CH565723A5/xx not_active IP Right Cessation
- 1971-06-22 GB GB2925771A patent/GB1338425A/en not_active Expired
- 1971-06-22 BE BE768850A patent/BE768850A/xx unknown
- 1971-06-22 US US00155649A patent/US3816552A/en not_active Expired - Lifetime
- 1971-06-23 SU SU1677039A patent/SU477575A3/ru active
- 1971-06-23 FR FR7122874A patent/FR2096789B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2096789A1 (enExample) | 1972-02-25 |
| CA943973A (en) | 1974-03-19 |
| CH565723A5 (enExample) | 1975-08-29 |
| BE768850A (fr) | 1971-12-22 |
| DE2031047A1 (enExample) | 1971-12-30 |
| NL7108425A (enExample) | 1971-12-28 |
| GB1338425A (en) | 1973-11-21 |
| US3816552A (en) | 1974-06-11 |
| FR2096789B1 (enExample) | 1975-08-22 |
| DE2031047B2 (de) | 1977-03-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3291843A (en) | Fluorinated vinyl ethers and their preparation | |
| Bartlett et al. | An acetylenic analog of neopentyl bromide; evidence that the hindrance to displacement reactions in neopentyl halides is steric in nature | |
| US2982786A (en) | Novel cyclic dimers of perfluorovinyl ethers | |
| SU477575A3 (ru) | Способ получени низших перфторалканов и циклических перфторолефинов | |
| Fowler et al. | Physical and chemical properties of pure fluorocarbons | |
| Chesick | THE KINETICS OF THE THERMAL DECOMPOSITION OF METHYLENECYCLOBUTANE1 | |
| US2733278A (en) | Process for preparing fluoroolefins | |
| Frey | Thermal unimolecular isomerization of 1-methylcyclobutene | |
| Pease et al. | Kinetics of Dissociation of Typical Hydrocarbon Vapors1 | |
| Turnbull et al. | A thermodynamic study of the dimerization of cyclopentadiene | |
| US3896179A (en) | Decomposition of unstable isomers | |
| Barbour et al. | The fluorination of hydrocarbons with cobalt trifluoride | |
| US3188356A (en) | Method for producing vinylidene fluoride | |
| US2413696A (en) | Fluorohydrocarbon | |
| US2709192A (en) | Process of preparing tetrafluoroethylene | |
| Blake et al. | The reaction of methyl radicals with formaldehyde | |
| US2436135A (en) | Halogenation of fluorinated compounds | |
| Morse et al. | Organic Fluorine Compounds: I. An Improved Synthesis of Hexafluoroacetone | |
| US2709182A (en) | Process for producing tetrafluoroethylene from perfluorocarbon having at least three carbon atoms | |
| US2401099A (en) | Reaction of 1, 3-dienes with polyhalogenated alkanes and products thereof | |
| Stull et al. | Thermodynamic properties of indane and indene | |
| Whipple | Vapor-liquid equilibria of some fluorinated hydrocarbon systems | |
| US2759983A (en) | Pyrolysis process for preparing hexafluoropropene from tetrafluoroethylene polymer | |
| Slabey | The reduction of pentaerythrityl tetrabromide in ethanol with zinc. Isolation of spiropentane | |
| US2773089A (en) | Fluorinated olefinic nitriles |