BE395649A - - Google Patents

Info

Publication number

BE395649A

BE395649A BE395649DA BE395649A BE 395649 A BE395649 A BE 395649A BE 395649D A BE395649D A BE 395649DA BE 395649 A BE395649 A BE 395649A

Authority

BE

Belgium

Prior art keywords

ethylene

gases

preparation

alcohol

process according

Prior art date

Links

• Espacenet
• Global Dossier
• Discuss

• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 24
• 239000007789 gas Substances 0.000 claims description 22
• 235000019441 ethanol Nutrition 0.000 claims description 19
• VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 17
• 239000005977 Ethylene Substances 0.000 claims description 17
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 10
• 238000000034 method Methods 0.000 claims description 10
• 239000000203 mixture Substances 0.000 claims description 10
• 239000003054 catalyst Substances 0.000 claims description 8
• 238000004519 manufacturing process Methods 0.000 claims description 8
• 238000002360 preparation method Methods 0.000 claims description 5
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
• 229930195733 hydrocarbon Natural products 0.000 claims description 4
• 150000002430 hydrocarbons Chemical class 0.000 claims description 4
• 238000011282 treatment Methods 0.000 claims description 4
• 238000006243 chemical reaction Methods 0.000 claims description 3
• BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 claims description 2
• 150000001298 alcohols Chemical class 0.000 claims description 2
• WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
• -1 propylene, butylene Chemical group 0.000 claims description 2
• 238000009833 condensation Methods 0.000 claims 1
• 230000005494 condensation Effects 0.000 claims 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
• VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
• 239000007788 liquid Substances 0.000 description 4
• 230000001476 alcoholic effect Effects 0.000 description 3
• 229910019142 PO4 Inorganic materials 0.000 description 2
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
• PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
• 230000015572 biosynthetic process Effects 0.000 description 2
• CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 2
• CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 2
• 229910000019 calcium carbonate Inorganic materials 0.000 description 2
• 235000010216 calcium carbonate Nutrition 0.000 description 2
• 230000036571 hydration Effects 0.000 description 2
• 238000006703 hydration reaction Methods 0.000 description 2
• 150000002576 ketones Chemical class 0.000 description 2
• QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
• 229910052753 mercury Inorganic materials 0.000 description 2
• 239000010452 phosphate Substances 0.000 description 2
• 239000002994 raw material Substances 0.000 description 2
• 239000000126 substance Substances 0.000 description 2
• KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
• 238000009825 accumulation Methods 0.000 description 1
• 230000003197 catalytic effect Effects 0.000 description 1
• 229910052593 corundum Inorganic materials 0.000 description 1
• KVIPHDKUOLVVQN-UHFFFAOYSA-N ethene;hydrate Chemical group O.C=C KVIPHDKUOLVVQN-UHFFFAOYSA-N 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
• 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
• 238000005057 refrigeration Methods 0.000 description 1
• 238000007127 saponification reaction Methods 0.000 description 1
• 238000003786 synthesis reaction Methods 0.000 description 1
• 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
• 238000009834 vaporization Methods 0.000 description 1
• 230000008016 vaporization Effects 0.000 description 1
• 229910001845 yogo sapphire Inorganic materials 0.000 description 1
• 235000014692 zinc oxide Nutrition 0.000 description 1
• RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1