BE446928A - - Google Patents

Info

Publication number

BE446928A

BE446928A BE446928DA BE446928A BE 446928 A BE446928 A BE 446928A BE 446928D A BE446928D A BE 446928DA BE 446928 A BE446928 A BE 446928A

Authority

BE

Belgium

Prior art keywords

wick

parts

mass

flame

mixture

Prior art date

Links

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• 239000000203 mixture Substances 0.000 claims description 13
• 150000001875 compounds Chemical class 0.000 claims description 8
• 238000002844 melting Methods 0.000 claims description 7
• 230000008018 melting Effects 0.000 claims description 7
• SOWBFZRMHSNYGE-UHFFFAOYSA-N oxamic acid Chemical compound NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 claims description 7
• 150000002148 esters Chemical class 0.000 claims description 6
• 239000000126 substance Substances 0.000 claims description 6
• 238000004040 coloring Methods 0.000 claims description 5
• WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
• XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 3
• TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 claims description 3
• 238000003825 pressing Methods 0.000 claims description 3
• 235000011037 adipic acid Nutrition 0.000 claims description 2
• 239000001361 adipic acid Substances 0.000 claims description 2
• 125000004494 ethyl ester group Chemical group 0.000 claims description 2
• 239000002360 explosive Substances 0.000 claims description 2
• 229910003002 lithium salt Inorganic materials 0.000 claims description 2
• 159000000002 lithium salts Chemical class 0.000 claims description 2
• 238000004519 manufacturing process Methods 0.000 claims description 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
• 229940082615 organic nitrates used in cardiac disease Drugs 0.000 claims description 2
• 238000000034 method Methods 0.000 claims 5
• 125000001931 aliphatic group Chemical group 0.000 claims 1
• 239000003292 glue Substances 0.000 claims 1
• WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 1
• 238000002485 combustion reaction Methods 0.000 description 3
• -1 aliphatic carbonic acids Chemical class 0.000 description 2
• 239000000470 constituent Substances 0.000 description 2
• 238000000354 decomposition reaction Methods 0.000 description 2
• PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
• RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
• WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
• 150000001408 amides Chemical class 0.000 description 1
• 229910052788 barium Inorganic materials 0.000 description 1
• DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
• 239000011230 binding agent Substances 0.000 description 1
• 230000008033 biological extinction Effects 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
• 239000004327 boric acid Substances 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
• 238000005266 casting Methods 0.000 description 1
• 238000006243 chemical reaction Methods 0.000 description 1
• 229910052802 copper Inorganic materials 0.000 description 1
• 239000010949 copper Substances 0.000 description 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
• 230000005496 eutectics Effects 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 150000002596 lactones Chemical class 0.000 description 1
• 229910052744 lithium Inorganic materials 0.000 description 1
• 239000000463 material Substances 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 150000002826 nitrites Chemical class 0.000 description 1
• LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
• 238000001556 precipitation Methods 0.000 description 1
• 230000002035 prolonged effect Effects 0.000 description 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 159000000008 strontium salts Chemical class 0.000 description 1
• 150000003475 thallium Chemical class 0.000 description 1
• 231100000331 toxic Toxicity 0.000 description 1
• 230000002588 toxic effect Effects 0.000 description 1