BE333744A - - Google Patents

Info

Publication number

BE333744A

BE333744A BE333744DA BE333744A BE 333744 A BE333744 A BE 333744A BE 333744D A BE333744D A BE 333744DA BE 333744 A BE333744 A BE 333744A

Authority

BE

Belgium

Prior art keywords

nitro

powders

aromatic

nitroglycerin

glycerin

Prior art date

Links

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• 229960003711 glyceryl trinitrate Drugs 0.000 description 15
• 239000000006 Nitroglycerin Substances 0.000 description 14
• 239000000843 powder Substances 0.000 description 14
• SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 13
• 239000000126 substance Substances 0.000 description 8
• 239000000374 eutectic mixture Substances 0.000 description 7
• 238000000034 method Methods 0.000 description 7
• 239000000020 Nitrocellulose Substances 0.000 description 5
• 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 5
• -1 aromatic nitro-derivatives Chemical class 0.000 description 5
• 125000003118 aryl group Chemical group 0.000 description 5
• 230000000694 effects Effects 0.000 description 5
• 229920001220 nitrocellulos Polymers 0.000 description 5
• 229940079938 nitrocellulose Drugs 0.000 description 5
• 239000004202 carbamide Substances 0.000 description 3
• 230000008018 melting Effects 0.000 description 3
• 238000002844 melting Methods 0.000 description 3
• 239000000203 mixture Substances 0.000 description 3
• 150000002828 nitro derivatives Chemical group 0.000 description 3
• XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
• SPSSULHKWOKEEL-UHFFFAOYSA-N 2,4,6-trinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O SPSSULHKWOKEEL-UHFFFAOYSA-N 0.000 description 2
• RMBFBMJGBANMMK-UHFFFAOYSA-N 2,4-dinitrotoluene Chemical compound CC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O RMBFBMJGBANMMK-UHFFFAOYSA-N 0.000 description 2
• 239000002360 explosive Substances 0.000 description 2
• 238000003475 lamination Methods 0.000 description 2
• 238000004519 manufacturing process Methods 0.000 description 2
• 238000006467 substitution reaction Methods 0.000 description 2
• 150000003672 ureas Chemical class 0.000 description 2
• PLAZTCDQAHEYBI-UHFFFAOYSA-N 2-nitrotoluene Chemical class CC1=CC=CC=C1[N+]([O-])=O PLAZTCDQAHEYBI-UHFFFAOYSA-N 0.000 description 1
• 241000238876 Acari Species 0.000 description 1
• 230000004075 alteration Effects 0.000 description 1
• 229920002678 cellulose Polymers 0.000 description 1
• 239000001913 cellulose Substances 0.000 description 1
• 238000007906 compression Methods 0.000 description 1
• 230000006835 compression Effects 0.000 description 1
• 238000002425 crystallisation Methods 0.000 description 1
• 230000008025 crystallization Effects 0.000 description 1
• 238000005213 imbibition Methods 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 238000000926 separation method Methods 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 238000003860 storage Methods 0.000 description 1