BE419138A - - Google Patents
Info
- Publication number
- BE419138A BE419138A BE419138DA BE419138A BE 419138 A BE419138 A BE 419138A BE 419138D A BE419138D A BE 419138DA BE 419138 A BE419138 A BE 419138A
- Authority
- BE
- Belgium
- Prior art keywords
- reaction
- equation
- methane
- cal
- basic
- Prior art date
Links
- 238000006243 chemical reaction Methods 0.000 claims description 125
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 93
- 229910001868 water Inorganic materials 0.000 claims description 33
- 239000000203 mixture Substances 0.000 claims description 32
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical class [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 20
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 17
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 16
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000007789 gas Substances 0.000 claims description 11
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 229910002090 carbon oxide Inorganic materials 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 230000008569 process Effects 0.000 claims description 5
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- -1 carbon anhydride Chemical class 0.000 claims description 3
- 239000001569 carbon dioxide Substances 0.000 claims description 2
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 7
- 230000002349 favourable effect Effects 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- 230000009471 action Effects 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 150000007824 aliphatic compounds Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 235000015096 spirit Nutrition 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 108010038629 Molybdoferredoxin Proteins 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- HBELESVMOSDEOV-UHFFFAOYSA-N [Fe].[Mo] Chemical compound [Fe].[Mo] HBELESVMOSDEOV-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000009830 intercalation Methods 0.000 description 1
- KWUUWVQMAVOYKS-UHFFFAOYSA-N iron molybdenum Chemical compound [Fe].[Fe][Mo][Mo] KWUUWVQMAVOYKS-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/86—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon
- C07C2/862—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by condensation between a hydrocarbon and a non-hydrocarbon the non-hydrocarbon contains only oxygen as hetero-atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE419138A true BE419138A (enExample) |
Family
ID=81497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE419138D BE419138A (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE419138A (enExample) |
-
0
- BE BE419138D patent/BE419138A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1258373A (fr) | Procede de fabrication de gaz de synthese utilisable notamment pour la production de methanol | |
| FR2937566A1 (fr) | Catalyseur d'hydrogenation, notamment de sulfure de carbone | |
| FR2667329A1 (fr) | Procede de production de fibres de carbone ayant des filaments en forme de serpentin. | |
| EP0004812B1 (fr) | Procédé de fabrication de nitroparaffines par nitration en phase gazeuse | |
| US3745209A (en) | Process for the preparation of vanadium(carbo)nitride | |
| EP0011602A1 (fr) | Composition d'alliage à base de titane et de fer pour le stockage de l'hydrogène | |
| FR2902786A1 (fr) | Procede de fabrication de 1,2-dichloroethane | |
| BE419138A (enExample) | ||
| DE2543788A1 (de) | Fluor und eine lewis-saeure enthaltende kohlenstoffverbindungen, ein verfahren zu ihrer herstellung sowie verfahren zur herstellung von abgeblaettertem graphit | |
| FR2736048A1 (fr) | Synthese du difluoromethane | |
| JPH0624720A (ja) | フッ素化フラーレンの製造方法 | |
| Luria et al. | Are HO radicals produced in the reaction of O (3P) with 1‐C4H8? | |
| US1438387A (en) | Manufacture of hydrogen | |
| US1253622A (en) | Manufacture of pure hydrogen. | |
| FR2880019A1 (fr) | Procede de fabrication de 1,2-dichloroethane | |
| US3522305A (en) | Production of urea and derivatives of ethylene and acetylene | |
| US553550A (en) | Process of producing illuminating-gas | |
| FR2582638A1 (fr) | Oxhydrures de terres rares et leur procede de preparation | |
| BE544849A (enExample) | ||
| BE464215A (enExample) | ||
| Lei | Computational Study of Nanomaterials: Properties, Syntheses, and Applications | |
| US1256272A (en) | Process for the synthetic production of cyanids. | |
| BE445727A (enExample) | ||
| CH270892A (fr) | Procédé de préparation d'un alliage dur et alliage obtenu par ce procédé. | |
| BE474881A (enExample) |