BE357711A - - Google Patents

Info

Publication number

BE357711A

BE357711A BE357711DA BE357711A BE 357711 A BE357711 A BE 357711A BE 357711D A BE357711D A BE 357711DA BE 357711 A BE357711 A BE 357711A

Authority

BE

Belgium

Prior art keywords

diphenyl

vapors

temperature

benzol

container

Prior art date

Links

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• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 29
• 239000004305 biphenyl Substances 0.000 claims description 25
• 235000010290 biphenyl Nutrition 0.000 claims description 25
• 125000006267 biphenyl group Chemical group 0.000 claims description 25
• ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 25
• 238000000034 method Methods 0.000 claims description 18
• 239000002184 metal Substances 0.000 claims description 12
• 238000001816 cooling Methods 0.000 claims description 4
• 229910052799 carbon Inorganic materials 0.000 claims description 3
• 239000007795 chemical reaction product Substances 0.000 claims 2
• 238000002360 preparation method Methods 0.000 claims 1
• 239000007789 gas Substances 0.000 description 7
• 238000004519 manufacturing process Methods 0.000 description 6
• 238000006243 chemical reaction Methods 0.000 description 4
• 238000005192 partition Methods 0.000 description 4
• 230000015572 biosynthetic process Effects 0.000 description 3
• 238000010438 heat treatment Methods 0.000 description 3
• 239000011261 inert gas Substances 0.000 description 3
• 239000007788 liquid Substances 0.000 description 3
• 238000007086 side reaction Methods 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
• WYTGDNHDOZPMIW-RCBQFDQVSA-N alstonine Natural products C1=CC2=C3C=CC=CC3=NC2=C2N1C[C@H]1[C@H](C)OC=C(C(=O)OC)[C@H]1C2 WYTGDNHDOZPMIW-RCBQFDQVSA-N 0.000 description 2
• 238000002485 combustion reaction Methods 0.000 description 2
• 229910052739 hydrogen Inorganic materials 0.000 description 2
• 239000001257 hydrogen Substances 0.000 description 2
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
• 230000001174 ascending effect Effects 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 239000001569 carbon dioxide Substances 0.000 description 1
• 229910002092 carbon dioxide Inorganic materials 0.000 description 1
• 238000004880 explosion Methods 0.000 description 1
• 238000004508 fractional distillation Methods 0.000 description 1
• 239000000446 fuel Substances 0.000 description 1
• FFNMBRCFFADNAO-UHFFFAOYSA-N pirenzepine hydrochloride Chemical compound [H+].[H+].[Cl-].[Cl-].C1CN(C)CCN1CC(=O)N1C2=NC=CC=C2NC(=O)C2=CC=CC=C21 FFNMBRCFFADNAO-UHFFFAOYSA-N 0.000 description 1
• 238000010517 secondary reaction Methods 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• 238000009834 vaporization Methods 0.000 description 1
• 230000008016 vaporization Effects 0.000 description 1