EA017229B1 - Способ конверсии углеводородного сырья с электролитическим извлечением галогенов - Google Patents
Способ конверсии углеводородного сырья с электролитическим извлечением галогенов Download PDFInfo
- Publication number
- EA017229B1 EA017229B1 EA200970960A EA200970960A EA017229B1 EA 017229 B1 EA017229 B1 EA 017229B1 EA 200970960 A EA200970960 A EA 200970960A EA 200970960 A EA200970960 A EA 200970960A EA 017229 B1 EA017229 B1 EA 017229B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- oxygen
- gas
- hydrogen
- hydrocarbons
- continuous method
- Prior art date
Links
- 150000002430 hydrocarbons Chemical class 0.000 title claims abstract description 145
- 229930195733 hydrocarbon Natural products 0.000 title claims abstract description 136
- 229910052736 halogen Inorganic materials 0.000 title claims abstract description 66
- 150000002367 halogens Chemical class 0.000 title claims abstract description 66
- 239000004215 Carbon black (E152) Substances 0.000 title claims abstract description 52
- 238000000034 method Methods 0.000 title description 55
- 230000008569 process Effects 0.000 title description 39
- 238000011084 recovery Methods 0.000 title description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 98
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000001301 oxygen Substances 0.000 claims abstract description 33
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 33
- 239000003345 natural gas Substances 0.000 claims abstract description 20
- 238000006243 chemical reaction Methods 0.000 claims description 51
- 239000001257 hydrogen Substances 0.000 claims description 47
- 229910052739 hydrogen Inorganic materials 0.000 claims description 47
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 45
- 239000007789 gas Substances 0.000 claims description 43
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 42
- 229910001868 water Inorganic materials 0.000 claims description 42
- 150000001350 alkyl halides Chemical class 0.000 claims description 37
- 229910000039 hydrogen halide Inorganic materials 0.000 claims description 36
- 239000012433 hydrogen halide Substances 0.000 claims description 36
- 239000003792 electrolyte Substances 0.000 claims description 25
- 239000003054 catalyst Substances 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 17
- 239000012528 membrane Substances 0.000 claims description 15
- 238000011437 continuous method Methods 0.000 claims description 14
- 238000009826 distribution Methods 0.000 claims description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 9
- 238000005341 cation exchange Methods 0.000 claims description 9
- 238000009792 diffusion process Methods 0.000 claims description 8
- 239000000446 fuel Substances 0.000 claims description 8
- 239000003570 air Substances 0.000 claims description 7
- 230000028161 membrane depolarization Effects 0.000 claims description 7
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 3
- 229910001882 dioxygen Inorganic materials 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- 150000003738 xylenes Chemical class 0.000 claims description 3
- 239000012736 aqueous medium Substances 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract description 144
- 230000015572 biosynthetic process Effects 0.000 abstract description 36
- 238000000926 separation method Methods 0.000 abstract description 29
- 238000010924 continuous production Methods 0.000 abstract description 15
- 230000026030 halogenation Effects 0.000 abstract description 4
- 238000005658 halogenation reaction Methods 0.000 abstract description 4
- 230000008929 regeneration Effects 0.000 abstract description 4
- 238000011069 regeneration method Methods 0.000 abstract description 4
- 150000001412 amines Chemical class 0.000 abstract description 3
- 230000001351 cycling effect Effects 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 62
- 239000000047 product Substances 0.000 description 62
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 58
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 56
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 54
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 41
- 229910052794 bromium Inorganic materials 0.000 description 41
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 35
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 31
- 238000005868 electrolysis reaction Methods 0.000 description 27
- 239000000571 coke Substances 0.000 description 23
- 238000009833 condensation Methods 0.000 description 22
- 230000005494 condensation Effects 0.000 description 22
- 238000005893 bromination reaction Methods 0.000 description 20
- 230000031709 bromination Effects 0.000 description 19
- 239000003245 coal Substances 0.000 description 19
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 18
- 239000003513 alkali Substances 0.000 description 17
- 229910001508 alkali metal halide Inorganic materials 0.000 description 16
- 150000008045 alkali metal halides Chemical class 0.000 description 16
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- 238000004821 distillation Methods 0.000 description 15
- 239000000243 solution Substances 0.000 description 15
- 239000002253 acid Substances 0.000 description 14
- 229940102396 methyl bromide Drugs 0.000 description 14
- 150000001347 alkyl bromides Chemical class 0.000 description 13
- -1 Br 2 Chemical class 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 12
- FJBFPHVGVWTDIP-UHFFFAOYSA-N dibromomethane Chemical compound BrCBr FJBFPHVGVWTDIP-UHFFFAOYSA-N 0.000 description 12
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 11
- 239000006096 absorbing agent Substances 0.000 description 11
- 238000010521 absorption reaction Methods 0.000 description 11
- 229910052799 carbon Inorganic materials 0.000 description 11
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 10
- 238000010586 diagram Methods 0.000 description 10
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 9
- 150000001335 aliphatic alkanes Chemical class 0.000 description 9
- 150000001336 alkenes Chemical class 0.000 description 9
- 235000019253 formic acid Nutrition 0.000 description 9
- 239000000543 intermediate Substances 0.000 description 9
- 238000003860 storage Methods 0.000 description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 8
- 239000006227 byproduct Substances 0.000 description 8
- 238000007323 disproportionation reaction Methods 0.000 description 8
- 230000005611 electricity Effects 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 8
- 238000007254 oxidation reaction Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 150000003973 alkyl amines Chemical class 0.000 description 7
- 239000002274 desiccant Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 229920005862 polyol Polymers 0.000 description 7
- 150000003077 polyols Chemical class 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000002028 Biomass Substances 0.000 description 6
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 238000004817 gas chromatography Methods 0.000 description 6
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- 238000006482 condensation reaction Methods 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- 239000001294 propane Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 239000010457 zeolite Substances 0.000 description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 229910021536 Zeolite Inorganic materials 0.000 description 4
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 description 4
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 4
- 238000005553 drilling Methods 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000036961 partial effect Effects 0.000 description 4
- 238000002407 reforming Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 3
- 229910001863 barium hydroxide Inorganic materials 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 229940006460 bromide ion Drugs 0.000 description 3
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 3
- 239000012295 chemical reaction liquid Substances 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000005265 energy consumption Methods 0.000 description 3
- UXKUODQYLDZXDL-UHFFFAOYSA-N fulminic acid Chemical compound [O-][N+]#C UXKUODQYLDZXDL-UHFFFAOYSA-N 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 230000003472 neutralizing effect Effects 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229940038384 octadecane Drugs 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 238000004445 quantitative analysis Methods 0.000 description 3
- 239000012047 saturated solution Substances 0.000 description 3
- 229910001415 sodium ion Inorganic materials 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 238000005576 amination reaction Methods 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 235000013844 butane Nutrition 0.000 description 2
- 229910002090 carbon oxide Inorganic materials 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- 101100458361 Drosophila melanogaster SmydA-8 gene Proteins 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000004280 Sodium formate Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001349 alkyl fluorides Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000003843 chloralkali process Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000006056 electrooxidation reaction Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000002140 halogenating effect Effects 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
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 230000004807 localization Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003606 oligomerizing effect Effects 0.000 description 1
- 238000013386 optimize process Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011027 product recovery Methods 0.000 description 1
- 238000011403 purification operation Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000006057 reforming reaction Methods 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/24—Halogens or compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B3/00—Electrolytic production of organic compounds
- C25B3/20—Processes
- C25B3/27—Halogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/26—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/26—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms
- C07C1/30—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only halogen atoms as hetero-atoms by splitting-off the elements of hydrogen halide from a single molecule
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/02—Alkenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
- C07C17/06—Preparation of halogenated hydrocarbons by addition of halogens combined with replacement of hydrogen atoms by halogens
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/06—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms
- C07C209/08—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
- C07C29/12—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of esters of mineral acids
- C07C29/124—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of esters of mineral acids of halides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
- C10B53/00—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
- C10B53/04—Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of powdered coal
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10B—DESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
- C10B57/00—Other carbonising or coking processes; Features of destructive distillation processes in general
- C10B57/04—Other carbonising or coking processes; Features of destructive distillation processes in general using charges of special composition
- C10B57/06—Other carbonising or coking processes; Features of destructive distillation processes in general using charges of special composition containing additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/02—Non-metals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K3/00—Modifying the chemical composition of combustible gases containing carbon monoxide to produce an improved fuel, e.g. one of different calorific value, which may be free from carbon monoxide
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/02—Hydrogen or oxygen
- C25B1/04—Hydrogen or oxygen by electrolysis of water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1011—Biomass
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1025—Natural gas
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/30—Aromatics
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/013—Alloys
- H01L2924/014—Solder alloys
-
- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
-
- 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
- Y02P20/141—Feedstock
- Y02P20/145—Feedstock the feedstock being materials of biological origin
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Metallurgy (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93022007P | 2007-05-14 | 2007-05-14 | |
PCT/US2008/006244 WO2008143940A2 (en) | 2007-05-14 | 2008-05-14 | Process for converting hydrocarbon feedstocks with electrolytic recovery of halogen |
Publications (2)
Publication Number | Publication Date |
---|---|
EA200970960A1 EA200970960A1 (ru) | 2010-04-30 |
EA017229B1 true EA017229B1 (ru) | 2012-10-30 |
Family
ID=40122241
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200970960A EA017229B1 (ru) | 2007-05-14 | 2008-05-14 | Способ конверсии углеводородного сырья с электролитическим извлечением галогенов |
EA201200888A EA201200888A1 (ru) | 2007-05-14 | 2008-05-14 | Способ конверсии углеводородного сырья с электролитическим извлечением галогенов |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201200888A EA201200888A1 (ru) | 2007-05-14 | 2008-05-14 | Способ конверсии углеводородного сырья с электролитическим извлечением галогенов |
Country Status (19)
Country | Link |
---|---|
US (1) | US20080314758A1 (OSRAM) |
EP (1) | EP2148942A4 (OSRAM) |
JP (1) | JP2010527358A (OSRAM) |
KR (1) | KR20100027135A (OSRAM) |
CN (1) | CN101687725A (OSRAM) |
AP (1) | AP2009005040A0 (OSRAM) |
AU (1) | AU2008254937C1 (OSRAM) |
BR (1) | BRPI0811606A2 (OSRAM) |
CA (1) | CA2684765A1 (OSRAM) |
CO (1) | CO6241174A2 (OSRAM) |
EA (2) | EA017229B1 (OSRAM) |
EC (1) | ECSP099732A (OSRAM) |
IN (1) | IN2009DN07232A (OSRAM) |
MX (1) | MX2009012353A (OSRAM) |
NO (1) | NO20093337L (OSRAM) |
NZ (1) | NZ580996A (OSRAM) |
TN (1) | TN2009000480A1 (OSRAM) |
WO (1) | WO2008143940A2 (OSRAM) |
ZA (1) | ZA200907775B (OSRAM) |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7838708B2 (en) | 2001-06-20 | 2010-11-23 | Grt, Inc. | Hydrocarbon conversion process improvements |
US20050171393A1 (en) | 2003-07-15 | 2005-08-04 | Lorkovic Ivan M. | Hydrocarbon synthesis |
CA2532367C (en) | 2003-07-15 | 2013-04-23 | Grt, Inc. | Hydrocarbon synthesis |
US8642822B2 (en) | 2004-04-16 | 2014-02-04 | Marathon Gtf Technology, Ltd. | Processes for converting gaseous alkanes to liquid hydrocarbons using microchannel reactor |
US20080275284A1 (en) | 2004-04-16 | 2008-11-06 | Marathon Oil Company | Process for converting gaseous alkanes to liquid hydrocarbons |
US20060229228A1 (en) * | 2005-04-11 | 2006-10-12 | Zachary John Anthony Komon | Method of making alkoxylates |
AU2007215476B2 (en) | 2006-02-03 | 2011-11-10 | Grt, Inc. | Continuous process for converting natural gas to liquid hydrocarbons |
US8921625B2 (en) | 2007-02-05 | 2014-12-30 | Reaction35, LLC | Continuous process for converting natural gas to liquid hydrocarbons |
WO2008148113A1 (en) | 2007-05-24 | 2008-12-04 | Grt, Inc. | Zone reactor incorporating reversible hydrogen halide capture and release |
US7696390B2 (en) * | 2008-06-10 | 2010-04-13 | Stauffer John E | Methanol synthesis |
US8282810B2 (en) * | 2008-06-13 | 2012-10-09 | Marathon Gtf Technology, Ltd. | Bromine-based method and system for converting gaseous alkanes to liquid hydrocarbons using electrolysis for bromine recovery |
US7812201B2 (en) | 2008-10-01 | 2010-10-12 | Targa Resources, Inc. | Process and catalyst for converting alkanes |
WO2010124041A1 (en) * | 2009-04-22 | 2010-10-28 | Grt, Inc. | Process for converting hydrocarbon feedstocks with electrolytic and photoelectrocatalytic recovery of halogens |
WO2010132325A1 (en) * | 2009-05-12 | 2010-11-18 | Shell Oil Company | An integrated process to produce hydrocarbons from natural gas containing carbon dioxide |
US8367884B2 (en) | 2010-03-02 | 2013-02-05 | Marathon Gtf Technology, Ltd. | Processes and systems for the staged synthesis of alkyl bromides |
US8815050B2 (en) | 2011-03-22 | 2014-08-26 | Marathon Gtf Technology, Ltd. | Processes and systems for drying liquid bromine |
US8436220B2 (en) * | 2011-06-10 | 2013-05-07 | Marathon Gtf Technology, Ltd. | Processes and systems for demethanization of brominated hydrocarbons |
US8829256B2 (en) | 2011-06-30 | 2014-09-09 | Gtc Technology Us, Llc | Processes and systems for fractionation of brominated hydrocarbons in the conversion of natural gas to liquid hydrocarbons |
US8802908B2 (en) | 2011-10-21 | 2014-08-12 | Marathon Gtf Technology, Ltd. | Processes and systems for separate, parallel methane and higher alkanes' bromination |
US9193641B2 (en) | 2011-12-16 | 2015-11-24 | Gtc Technology Us, Llc | Processes and systems for conversion of alkyl bromides to higher molecular weight hydrocarbons in circulating catalyst reactor-regenerator systems |
US9702049B1 (en) * | 2012-05-14 | 2017-07-11 | Melahn L. Parker | Biowaste treatment and recovery system |
US11167242B1 (en) | 2012-05-14 | 2021-11-09 | Chemergy, Inc. | Process for desulpherization and hydrogen recovery |
US10329676B2 (en) | 2012-07-26 | 2019-06-25 | Avantium Knowledge Centre B.V. | Method and system for electrochemical reduction of carbon dioxide employing a gas diffusion electrode |
US8641885B2 (en) | 2012-07-26 | 2014-02-04 | Liquid Light, Inc. | Multiphase electrochemical reduction of CO2 |
US9267212B2 (en) | 2012-07-26 | 2016-02-23 | Liquid Light, Inc. | Method and system for production of oxalic acid and oxalic acid reduction products |
US9175407B2 (en) | 2012-07-26 | 2015-11-03 | Liquid Light, Inc. | Integrated process for producing carboxylic acids from carbon dioxide |
US20130105304A1 (en) | 2012-07-26 | 2013-05-02 | Liquid Light, Inc. | System and High Surface Area Electrodes for the Electrochemical Reduction of Carbon Dioxide |
US8845876B2 (en) | 2012-07-26 | 2014-09-30 | Liquid Light, Inc. | Electrochemical co-production of products with carbon-based reactant feed to anode |
WO2014043651A2 (en) | 2012-09-14 | 2014-03-20 | Liquid Light, Inc. | High pressure electrochemical cell and process for the electrochemical reduction of carbon dioxide |
WO2014138252A1 (en) * | 2013-03-06 | 2014-09-12 | Ceramatec, Inc. | Method of producing coupled radical products via desulfoxylation |
WO2014193957A1 (en) * | 2013-05-30 | 2014-12-04 | Reaction 35, Llc | Recovery of halogens by partial condensation |
CN104947139B (zh) * | 2013-10-21 | 2017-05-03 | 中国民用航空飞行学院 | 一种煤电化液化电解方法 |
CN103952717A (zh) * | 2014-05-07 | 2014-07-30 | 北京化工大学 | 一种光电化学分解水与有机合成相互耦合的串联反应设计方法 |
US20170121831A1 (en) * | 2014-06-19 | 2017-05-04 | Liquid Light, Inc. | Integrated Process for Co-Production of Carboxylic Acids and Halogen Products from Carbon Dioxide |
KR102291922B1 (ko) | 2015-04-28 | 2021-08-20 | 대우조선해양 주식회사 | 천연가스를 이용하여 중질탄화수소를 생산하는 flng 및 flng에서 천연가스를 이용하여 중질탄화수소를 생산하는 방법 |
WO2019067784A1 (en) * | 2017-09-27 | 2019-04-04 | The Trustees Of The Stevens Institute Of Technology | PROCESS AND APPARATUS FOR RECOVERING AND CONVERTING ALKYL HALIDE FUMIGANT |
CN109608329A (zh) * | 2018-12-12 | 2019-04-12 | 浙江大学 | 一种低溴排放的对苯二甲酸生产方法 |
EP4126797A1 (en) | 2020-03-30 | 2023-02-08 | Totalenergies Onetech | Gas to hydrogen process with co-production of carbon |
US11739035B2 (en) | 2020-03-30 | 2023-08-29 | Totalenergies Onetech | Gas to olefins processes with coproduction of hydrogen |
WO2021198166A1 (en) | 2020-03-30 | 2021-10-07 | Total Se | Gas to olefins process with coproduction of hydrogen together with heat integration process |
WO2021198175A1 (en) | 2020-03-30 | 2021-10-07 | Total Se | Gas to olefins process with coproduction of hydrogen together with electrified reactional section |
CN111607442A (zh) * | 2020-05-15 | 2020-09-01 | 重庆燃气集团股份有限公司 | 一种天然气储气调峰的综合能源利用体系及储气调峰方法 |
WO2021239811A1 (en) | 2020-05-29 | 2021-12-02 | Total Se | Gas to methanol with coproduction of hydrogen |
DE102020212022A1 (de) | 2020-07-09 | 2022-01-13 | Siemens Aktiengesellschaft | Verfahren und Vorrichtung zur Herstellung von Kohlenmonoxid aus Kohlendioxid |
EP4561970A1 (en) * | 2022-07-25 | 2025-06-04 | TotalEnergies OneTech | Process for the production of dimethyl ether and hydrogen from methane using a solid metal oxide reagent |
CN115491697B (zh) * | 2022-10-21 | 2023-09-08 | 上海科技大学 | 一种烃类原料高效转化的方法及其装置 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2824891A (en) * | 1955-11-07 | 1958-02-25 | Universal Oil Prod Co | Surface active agents derived from aromatic aldehyde intermediates |
US4333805A (en) * | 1980-05-02 | 1982-06-08 | General Electric Company | Halogen evolution with improved anode catalyst |
US4732660A (en) * | 1985-09-09 | 1988-03-22 | The Dow Chemical Company | Membrane electrolyzer |
JPH0977707A (ja) * | 1995-09-13 | 1997-03-25 | Hironori Ishikawa | 水熱法によるメタノール等の燃料用アルコール類の合成法 |
US5998679A (en) * | 1998-05-20 | 1999-12-07 | Jlm Technology, Ltd. | Methods for converting lower alkanes and alkanes to alcohols and diols |
US6368490B1 (en) * | 1997-12-15 | 2002-04-09 | Bayer Aktiengesellschaft | Method for electrochemically processing HCL gas into highly pure chlorine |
US20050234277A1 (en) * | 2004-04-16 | 2005-10-20 | Waycuilis John J | Process for converting gaseous alkanes to liquid hydrocarbons |
Family Cites Families (106)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1037137B (de) * | 1957-01-25 | 1958-08-21 | Bayer Ag | Verfahren zur Herstellung halogenhaltiger, aromatisch-aliphatischer Polyaether |
US3562321A (en) * | 1961-10-10 | 1971-02-09 | Sun Oil Co | Preparation of oxygenated hydrocarbons |
US3496242A (en) * | 1967-08-30 | 1970-02-17 | Fmc Corp | Oxychlorination of mixed hydrocarbons |
US3865886A (en) * | 1973-06-20 | 1975-02-11 | Lummus Co | Production of allyl chloride |
US4138440A (en) * | 1974-08-14 | 1979-02-06 | Mobil Oil Corporation | Conversion of liquid alcohols and ethers with a fluid mass of ZSM-5 type catalyst |
US4071753A (en) * | 1975-03-31 | 1978-01-31 | Gte Laboratories Incorporated | Transducer for converting acoustic energy directly into optical energy |
US4133838A (en) * | 1975-05-15 | 1979-01-09 | Pearson Research Corp. | Process for preparing hydrocarbons from methanol and phosphorus pentoxide |
US4006169A (en) * | 1976-02-26 | 1977-02-01 | Smithkline Corporation | Epoxidation of α,β-ethylenic ketones |
US4072733A (en) * | 1976-04-02 | 1978-02-07 | Ethyl Corporation | Conversion of methanol and dimethyl ether |
US4133966A (en) * | 1977-12-23 | 1979-01-09 | Gulf Research & Development Company | Selective formation of ethanol from methanol, hydrogen and carbon monoxide |
US4191618A (en) * | 1977-12-23 | 1980-03-04 | General Electric Company | Production of halogens in an electrolysis cell with catalytic electrodes bonded to an ion transporting membrane and an oxygen depolarized cathode |
US4187255A (en) * | 1978-08-21 | 1980-02-05 | Conoco, Inc. | Process for methylating naphthalene |
US4311865A (en) * | 1979-04-04 | 1982-01-19 | Mobil Oil Corporation | Manufacture of hydrocarbons from oxygenates |
NL7902886A (nl) * | 1979-04-12 | 1980-10-14 | Shell Int Research | Werkwijze voor de bereiding van een koolwaterstof- mengsel. |
US4496752A (en) * | 1979-05-03 | 1985-01-29 | The Lummus Company | Production of epoxy compounds from olefinic compounds |
US4371716A (en) * | 1979-09-04 | 1983-02-01 | Shell Oil Company | β-(Sec-alkoxy) ethanol process |
US4431856A (en) * | 1980-09-29 | 1984-02-14 | Mobil Oil Corporation | Fluid zeolite catalyst conversion of alcohols and oxygenated derivatives to hydrocarbons |
US4373109A (en) * | 1981-08-05 | 1983-02-08 | Olah George A | Bifunctional acid-base catalyzed conversion of hetero-substituted methanes into olefins |
US4433192A (en) * | 1981-09-01 | 1984-02-21 | Olah George A | Condensation of natural gas or methane into gasoline range hydrocarbons |
US4568660A (en) * | 1982-01-25 | 1986-02-04 | Hercules Incorporated | Cycloolefin polymerization catalyst composition |
US4433189A (en) * | 1982-03-18 | 1984-02-21 | Mobil Oil Corporation | Catalytic conversion of methanol to light olefins |
US4499314A (en) * | 1982-03-31 | 1985-02-12 | Imperial Chemical Industries Plc | Methanol conversion to hydrocarbons with zeolites and cocatalysts |
DE3216722A1 (de) * | 1982-05-05 | 1983-11-10 | Hoechst Ag, 6230 Frankfurt | 4-halomethylbenzoesaeure-alkylester-imine und verfahren zu deren herstellung |
US4720600A (en) * | 1983-06-29 | 1988-01-19 | Mobil Oil Corporation | Production of middle distillate range hydrocarbons by light olefin upgrading |
US4642404A (en) * | 1984-01-23 | 1987-02-10 | Mobil Oil Corporation | Conversion of olefins and paraffins to higher hydrocarbons |
US4634800A (en) * | 1984-04-16 | 1987-01-06 | Atlantic Richfield Company | Methane conversion process |
US4497967A (en) * | 1984-06-15 | 1985-02-05 | The Halcon Sd Group, Inc. | Process for the preparation of ethanol from methanol, carbon monoxide _and hydrogen |
GB8429007D0 (en) * | 1984-11-16 | 1984-12-27 | British Petroleum Co Plc | Aromatics from ethane/ethylene |
US4764356A (en) * | 1984-12-21 | 1988-08-16 | Exxon Research & Engineering Co. | Process for synthesizing a zeolite catalyst on a pH controlled basis to improve catalyst life |
US4724275A (en) * | 1985-07-01 | 1988-02-09 | National Distillers And Chemical Corporation | Crystalline aluminosilicates and their use in the conversion of methanol to low molecular weight hydrocarbons |
GB8518820D0 (en) * | 1985-07-25 | 1985-08-29 | British Petroleum Co Plc | Chemical process |
US4795843A (en) * | 1985-08-26 | 1989-01-03 | Uop Inc. | Conversion of methane into larger organic hydrocarbons |
ZA874948B (en) * | 1986-07-07 | 1989-02-22 | Mobil Oil Corp | Aromatisation of aliphatics over gallium-containing zeolites |
US4795848A (en) * | 1986-08-28 | 1989-01-03 | The Standard Oil Company | Method for upgrading a low molecular weight alkane with a lead-zirconate catalyst |
US5082816A (en) * | 1986-08-28 | 1992-01-21 | The Standard Oil Company | Lead-zirconate catalysts |
US4720602A (en) * | 1986-09-08 | 1988-01-19 | Mobil Oil Corporation | Process for converting C2 to C12 aliphatics to aromatics over a zinc-activated zeolite |
US5087787A (en) * | 1986-12-29 | 1992-02-11 | Phillips Petroleum Company | Method of oxidative conversion |
US4795737A (en) * | 1987-03-25 | 1989-01-03 | Eastman Kodak Company | Process for the iodination of aromatic compounds over solid catalysts |
US4808763A (en) * | 1987-08-05 | 1989-02-28 | Amoco Corporation | Process for upgrading light paraffins |
US4804797A (en) * | 1987-08-24 | 1989-02-14 | Gas Research Institute | Production of commodity chemicals from natural gas by methane chlorination |
US4990711A (en) * | 1988-06-23 | 1991-02-05 | Mobil Oil Corporation | Synthetic polyolefin lubricant blends having high viscosity indices |
US4899002A (en) * | 1988-07-25 | 1990-02-06 | Mobil Oil Corp. | Integrated staged conversion of methanol to gasoline and distillate |
US4899001A (en) * | 1988-11-21 | 1990-02-06 | Uop | Process for the simultaneous hydroconversion of a first feedstock comprising unsaturated, halogenated organic compounds and a second feedstock comprising saturated, halogenated organic compounds |
US4895995A (en) * | 1988-12-02 | 1990-01-23 | Uop | Process for the simultaneous hydroconversion of a first feedstock comprising unsaturated, halogenated organic compounds and a second feedstock comprising saturated, halogenated organic compounds |
US5178748A (en) * | 1988-12-22 | 1993-01-12 | Imperial Chemical Industries | Catalytic reactions using zeolites |
US4990696A (en) * | 1988-12-29 | 1991-02-05 | Stauffer John E | Methyl alcohol process |
US4899000A (en) * | 1989-01-27 | 1990-02-06 | Stauffer John E | Production of allyl chloride |
US4982024A (en) * | 1989-12-26 | 1991-01-01 | Ethyl Corporation | Process for the selective dehydrohalogenation of an admixture of alkylhalides |
US4982041A (en) * | 1990-01-10 | 1991-01-01 | Union Carbide Chemicals And Plastics Company Inc. | Double perovskite catalysts for oxidative coupling |
US5087786A (en) * | 1990-04-25 | 1992-02-11 | Amoco Corporation | Halogen-assisted conversion of lower alkanes |
US5087779A (en) * | 1990-04-25 | 1992-02-11 | Amoco Corporation | Hydrocarbon halogenation |
US5068478A (en) * | 1990-05-25 | 1991-11-26 | Energia Andina, Ltd. | Producing alkenes and alkynes from alkanes and alkenes |
GB9013859D0 (en) * | 1990-06-21 | 1990-08-15 | Ici Plc | Zeolites |
US4988660A (en) * | 1990-06-25 | 1991-01-29 | Union Carbide Chemicals And Plastics Company Inc. | Double perovskite catalysts for oxidative coupling |
US5082473A (en) * | 1990-07-23 | 1992-01-21 | Keefer Bowie | Extraction and concentration of a gas component |
US5085674A (en) * | 1990-10-25 | 1992-02-04 | Union Carbide Industrial Gases Technology Corporation | Duplex adsorption process |
EP0584074B1 (en) * | 1990-12-06 | 1996-07-03 | Occidental Chemical Corporation | A process for the production of ethylene or a mixture of ethylene and vinyl chloride |
US5188725A (en) * | 1991-03-15 | 1993-02-23 | Mobil Oil Corporation | Fluidized catalyst process for production and etherification of olefins |
US5276240A (en) * | 1991-10-18 | 1994-01-04 | Board Of Regents, The University Of Texas System | Catalytic hydrodehalogenation of polyhalogenated hydrocarbons |
US5385650A (en) * | 1991-11-12 | 1995-01-31 | Great Lakes Chemical Corporation | Recovery of bromine and preparation of hypobromous acid from bromide solution |
US6169218B1 (en) * | 1992-02-10 | 2001-01-02 | Catalytic Distillation Technologies | Selective hydrogenation of highly unsaturated compounds in hydrocarbon streams |
US5185479A (en) * | 1992-04-21 | 1993-02-09 | Stauffer John E | Process for methyl alcohol |
CA2097090A1 (en) * | 1992-06-02 | 1993-12-03 | Quang N. Le | Process for the production of tertiary alkyl ether rich fcc gasoline |
US5284990A (en) * | 1992-07-16 | 1994-02-08 | Stratco, Inc. | Method for converting a hydrogen fluoride alkylation unit to a sulfuric acid alkylation unit |
US5276242A (en) * | 1992-08-26 | 1994-01-04 | Phillips Petroleum Company | Alkylation process |
US5276226A (en) * | 1992-10-05 | 1994-01-04 | Exxon Research & Engineering Company | Low temperature halogenation of alkanes |
TW291486B (OSRAM) * | 1992-12-17 | 1996-11-21 | Exxon Chemical Patents Inc | |
US5470377A (en) * | 1993-03-08 | 1995-11-28 | Whitlock; David R. | Separation of solutes in gaseous solvents |
US5382743A (en) * | 1993-04-26 | 1995-01-17 | Mobil Oil Corporation | Skeletal isomerization of n-pentenes using ZSM-35 in the presence of hydrogen |
US5382704A (en) * | 1993-06-30 | 1995-01-17 | E. I. Du Pont De Nemours And Company | Fluorinated methyl ethers |
US5382744A (en) * | 1993-07-12 | 1995-01-17 | Phillips Petroleum Company | Control of synthetic isopentane production during alkylation of amylenes |
US5500297A (en) * | 1993-08-09 | 1996-03-19 | The Trustees Of Princeton University | Electron acceptor compositions technical field |
US5600045A (en) * | 1993-12-02 | 1997-02-04 | The Dow Chemical Company | Process for conversion of crude hydrocarbon mixtures |
EP0704424B1 (en) * | 1994-09-28 | 1998-12-30 | Showa Denko Kabushiki Kaisha | 3-Alkoxypropionic ester derivative, olefin polymerization catalyst, and process for preparation of polyolefin |
GB2294262B (en) * | 1994-10-20 | 1998-07-08 | Evc Tech Ag | Single stage fixed bed oxychlorination of ethylene |
US5489727A (en) * | 1994-10-28 | 1996-02-06 | Phillips Petroleum Company | Isopentane disproportionation |
US5486627A (en) * | 1994-12-02 | 1996-01-23 | The Dow Chemical Company | Method for producing epoxides |
US5600043A (en) * | 1995-03-27 | 1997-02-04 | The Geon Company | Oxychlorination process |
DE69523077T2 (de) * | 1995-05-01 | 2002-06-06 | E.I. Du Pont De Nemours And Co., Wilmington | Elektrochemische umwandlung von wasserfreiem halogenwasserstoff in halogengas mittels einer kationenaustauschermembran |
US5705712A (en) * | 1995-10-05 | 1998-01-06 | Uop | Integrated process for producing diisopropyl ether, an isopropyl tertiary alkyl ether and isopropyl alcohol |
US5705729A (en) * | 1995-11-22 | 1998-01-06 | Mobil Oil Corporation | Isoparaffin-olefin alkylation process |
IN192223B (OSRAM) * | 1995-12-28 | 2004-03-20 | Du Pont | |
AU692723B2 (en) * | 1996-02-01 | 1998-06-11 | Phillips Petroleum Company | Catalyst composition and process for selecting hydrogenation of diolefins |
US5720858A (en) * | 1996-07-17 | 1998-02-24 | The United States Of America As Represented By The United States Department Of Energy | Method for the photocatalytic conversion of methane |
US5708246A (en) * | 1996-08-28 | 1998-01-13 | Battelle Memorial Institute | Method of photocatalytic conversion of C-H organics |
US6018088A (en) * | 1997-05-07 | 2000-01-25 | Olah; George A. | Superacid catalyzed formylation-rearrangement of saturated hydrocarbons |
EP0999182B1 (fr) * | 1998-11-02 | 2003-05-14 | Institut Francais Du Petrole | Procédé de préparation d'une zéolithe de type structural EUO à l'aide de germes de matériaux zéolitiques et son utilisation comme catalyseur d'isomérisation des aromatiques à huit atomes de carbone |
DK0999183T3 (da) * | 1998-11-02 | 2003-07-14 | Inst Francais Du Petrole | Fremgangsmåde til fremstilling af en zeolit af strukturtypen EUO ved hjælp af forstadier til det strukturerende middel og anvendelse heraf som katalysator til isomerisering af AC8 |
US6936565B2 (en) * | 1999-01-12 | 2005-08-30 | Hyperion Catalysis International, Inc. | Modified carbide and oxycarbide containing catalysts and methods of making and using thereof |
FR2793706B1 (fr) * | 1999-05-18 | 2001-08-03 | Total Raffinage Distribution | Support catalytique a base d'oxyde d'un metal du groupe ivb de la classification periodique des elements, sa preparation et ses utilisations |
US6680415B1 (en) * | 1999-11-22 | 2004-01-20 | Dow Global Technologies Inc. | Oxyhalogenation process using catalyst having porous rare earth halide support |
IT1317753B1 (it) * | 2000-02-02 | 2003-07-15 | Nora S P A Ora De Nora Impiant | Cella di elettrolisi con elettrodo a diffusione di gas. |
DE60130758T2 (de) * | 2000-05-31 | 2008-05-21 | Chevron U.S.A. Inc., San Ramon | Zeolith ssz-53 |
FR2813809B1 (fr) * | 2000-09-11 | 2003-07-25 | Air Liquide | Colonne a garnissage d'echange de chaleur et/ou de matiere |
PL355422A1 (en) * | 2000-11-29 | 2004-04-19 | Vinnolit Technologie Gmbh & Co.Kg | Method for producing 1,2-dichloroethane |
US6511526B2 (en) * | 2001-01-12 | 2003-01-28 | Vbox, Incorporated | Pressure swing adsorption gas separation method and apparatus |
US6509485B2 (en) * | 2001-02-22 | 2003-01-21 | Sri International | Preparation of epoxides from alkanes using lanthanide-promoted silver catalysts |
CN100424056C (zh) * | 2001-05-23 | 2008-10-08 | 陶氏环球技术公司 | C3+烃的氧化卤化和任选脱氢反应 |
US7161050B2 (en) * | 2001-06-20 | 2007-01-09 | Grt, Inc. | Method and apparatus for synthesizing olefins, alcohols, ethers, and aldehydes |
US6685821B2 (en) * | 2001-08-29 | 2004-02-03 | Giner Electrochemical Systems, Llc | Method and system for producing high-pressure hydrogen |
CA2532367C (en) * | 2003-07-15 | 2013-04-23 | Grt, Inc. | Hydrocarbon synthesis |
GB0320684D0 (en) * | 2003-09-03 | 2003-10-01 | Bp Chem Int Ltd | Process |
US6838576B1 (en) * | 2003-10-23 | 2005-01-04 | 3M Innovative Properties Company | Process for preparing functional group-containing olefinic compounds |
EP1735255A4 (en) * | 2004-04-16 | 2012-01-04 | Marathon Gtf Technology Ltd | METHOD FOR CONVERTING GASEOUS ALKANS IN LIQUID HYDROCARBONS |
US20060100469A1 (en) * | 2004-04-16 | 2006-05-11 | Waycuilis John J | Process for converting gaseous alkanes to olefins and liquid hydrocarbons |
AU2007215476B2 (en) * | 2006-02-03 | 2011-11-10 | Grt, Inc. | Continuous process for converting natural gas to liquid hydrocarbons |
-
2008
- 2008-05-14 IN IN7232DEN2009 patent/IN2009DN07232A/en unknown
- 2008-05-14 CA CA002684765A patent/CA2684765A1/en not_active Abandoned
- 2008-05-14 BR BRPI0811606A patent/BRPI0811606A2/pt not_active IP Right Cessation
- 2008-05-14 EA EA200970960A patent/EA017229B1/ru not_active IP Right Cessation
- 2008-05-14 WO PCT/US2008/006244 patent/WO2008143940A2/en active Application Filing
- 2008-05-14 NZ NZ580996A patent/NZ580996A/en not_active IP Right Cessation
- 2008-05-14 KR KR1020097025908A patent/KR20100027135A/ko not_active Withdrawn
- 2008-05-14 EP EP08754498A patent/EP2148942A4/en not_active Withdrawn
- 2008-05-14 US US12/152,515 patent/US20080314758A1/en not_active Abandoned
- 2008-05-14 EA EA201200888A patent/EA201200888A1/ru unknown
- 2008-05-14 AU AU2008254937A patent/AU2008254937C1/en not_active Expired - Fee Related
- 2008-05-14 JP JP2010508428A patent/JP2010527358A/ja active Pending
- 2008-05-14 AP AP2009005040A patent/AP2009005040A0/en unknown
- 2008-05-14 CN CN200880016076A patent/CN101687725A/zh active Pending
- 2008-05-14 MX MX2009012353A patent/MX2009012353A/es unknown
-
2009
- 2009-11-05 ZA ZA200907775A patent/ZA200907775B/xx unknown
- 2009-11-10 TN TNP2009000480A patent/TN2009000480A1/fr unknown
- 2009-11-13 NO NO20093337A patent/NO20093337L/no not_active Application Discontinuation
- 2009-11-13 EC EC2009009732A patent/ECSP099732A/es unknown
- 2009-11-13 CO CO09129699A patent/CO6241174A2/es not_active Application Discontinuation
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2824891A (en) * | 1955-11-07 | 1958-02-25 | Universal Oil Prod Co | Surface active agents derived from aromatic aldehyde intermediates |
US4333805A (en) * | 1980-05-02 | 1982-06-08 | General Electric Company | Halogen evolution with improved anode catalyst |
US4732660A (en) * | 1985-09-09 | 1988-03-22 | The Dow Chemical Company | Membrane electrolyzer |
JPH0977707A (ja) * | 1995-09-13 | 1997-03-25 | Hironori Ishikawa | 水熱法によるメタノール等の燃料用アルコール類の合成法 |
US6368490B1 (en) * | 1997-12-15 | 2002-04-09 | Bayer Aktiengesellschaft | Method for electrochemically processing HCL gas into highly pure chlorine |
US5998679A (en) * | 1998-05-20 | 1999-12-07 | Jlm Technology, Ltd. | Methods for converting lower alkanes and alkanes to alcohols and diols |
US20050234277A1 (en) * | 2004-04-16 | 2005-10-20 | Waycuilis John J | Process for converting gaseous alkanes to liquid hydrocarbons |
Also Published As
Publication number | Publication date |
---|---|
WO2008143940A3 (en) | 2009-12-30 |
EA201200888A1 (ru) | 2013-02-28 |
ZA200907775B (en) | 2010-07-28 |
IN2009DN07232A (OSRAM) | 2015-07-24 |
EA200970960A1 (ru) | 2010-04-30 |
ECSP099732A (es) | 2010-02-26 |
NO20093337L (no) | 2010-02-12 |
CO6241174A2 (es) | 2011-01-20 |
AU2008254937C1 (en) | 2013-05-30 |
AU2008254937A1 (en) | 2008-11-27 |
CN101687725A (zh) | 2010-03-31 |
BRPI0811606A2 (pt) | 2019-09-24 |
AP2009005040A0 (en) | 2009-12-31 |
KR20100027135A (ko) | 2010-03-10 |
TN2009000480A1 (en) | 2011-03-31 |
CA2684765A1 (en) | 2008-11-27 |
WO2008143940A2 (en) | 2008-11-27 |
EP2148942A4 (en) | 2011-11-09 |
EP2148942A2 (en) | 2010-02-03 |
MX2009012353A (es) | 2010-02-17 |
US20080314758A1 (en) | 2008-12-25 |
AU2008254937B2 (en) | 2013-01-17 |
JP2010527358A (ja) | 2010-08-12 |
NZ580996A (en) | 2011-09-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EA017229B1 (ru) | Способ конверсии углеводородного сырья с электролитическим извлечением галогенов | |
US20100270167A1 (en) | Process for converting hydrocarbon feedstocks with electrolytic and photoelectrocatalytic recovery of halogens | |
KR101433781B1 (ko) | 탄화수소를 형성하기 위한 시스템 및 방법 | |
CA2727545C (en) | Bromine-based method and system for converting gaseous alkanes to liquid hydrocarbons using electrolysis for bromine recovery | |
CA2727544C (en) | Hydrogenation of multi-brominated alkanes | |
KR101740419B1 (ko) | 천연 가스를 액체 탄화수소로 변환시키는 연속 공정 | |
AU2017209876B2 (en) | Electrolysis system and method for electrochemical ethylene oxide production | |
EA022995B1 (ru) | Непрерывный способ превращения природного газа в жидкие углеводороды | |
KR101356630B1 (ko) | 원자력 수소 생산용 하이브리드형 요오드화수소 분해장치 및 이를 이용한 연속 수소 분해 방법 | |
US12209322B2 (en) | Chlor-alkali and carbon monoxide electrolyzer integration | |
HK1147739A (en) | Continuous process for converting natural gas to liquid hydrocarbons | |
HK1171437A (en) | Continuous process for converting natural gas to liquid hydrocarbons |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM RU |