BE438289A - - Google Patents

Info

Publication number

BE438289A

BE438289A BE438289DA BE438289A BE 438289 A BE438289 A BE 438289A BE 438289D A BE438289D A BE 438289DA BE 438289 A BE438289 A BE 438289A

Authority

BE

Belgium

Prior art keywords

sep

acid

liquid

luminescent material

acetone

Prior art date

Links

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• 239000002904 solvent Substances 0.000 claims description 16
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 14
• 238000000034 method Methods 0.000 claims description 14
• 239000002253 acid Substances 0.000 claims description 11
• 239000007788 liquid Substances 0.000 claims description 11
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
• KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 6
• 239000004327 boric acid Substances 0.000 claims description 6
• 229920002678 cellulose Polymers 0.000 claims description 5
• 238000010438 heat treatment Methods 0.000 claims description 5
• 239000004014 plasticizer Substances 0.000 claims description 5
• DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 4
• 230000002378 acidificating effect Effects 0.000 claims description 3
• 229920002301 cellulose acetate Polymers 0.000 claims description 3
• 150000001875 compounds Chemical class 0.000 claims description 2
• 239000001913 cellulose Substances 0.000 claims 1
• 239000000463 material Substances 0.000 description 19
• 239000011521 glass Substances 0.000 description 9
• 150000002148 esters Chemical class 0.000 description 7
• 239000011230 binding agent Substances 0.000 description 4
• 239000000203 mixture Substances 0.000 description 4
• 239000000725 suspension Substances 0.000 description 4
• 239000000020 Nitrocellulose Substances 0.000 description 3
• FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 3
• QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
• 229910052753 mercury Inorganic materials 0.000 description 3
• 229920001220 nitrocellulos Polymers 0.000 description 3
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
• 150000007513 acids Chemical class 0.000 description 2
• 229910052799 carbon Inorganic materials 0.000 description 2
• 238000000151 deposition Methods 0.000 description 2
• 229910052752 metalloid Inorganic materials 0.000 description 2
• 150000002738 metalloids Chemical class 0.000 description 2
• 238000005096 rolling process Methods 0.000 description 2
• 239000007787 solid Substances 0.000 description 2
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
• BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
• 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
• 229910052785 arsenic Inorganic materials 0.000 description 1
• RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 150000001721 carbon Chemical class 0.000 description 1
• 238000002485 combustion reaction Methods 0.000 description 1
• 239000000470 constituent Substances 0.000 description 1
• 238000000354 decomposition reaction Methods 0.000 description 1
• 230000008021 deposition Effects 0.000 description 1
• 230000000694 effects Effects 0.000 description 1
• 230000002349 favourable effect Effects 0.000 description 1
• 230000004927 fusion Effects 0.000 description 1
• 238000007429 general method Methods 0.000 description 1
• 235000011187 glycerol Nutrition 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 150000002894 organic compounds Chemical class 0.000 description 1
• WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
• XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1