EP2128117A2 - Modifizierungsmittel für sprengstoffe - Google Patents
Modifizierungsmittel für sprengstoffe Download PDFInfo
- Publication number
- EP2128117A2 EP2128117A2 EP07861028A EP07861028A EP2128117A2 EP 2128117 A2 EP2128117 A2 EP 2128117A2 EP 07861028 A EP07861028 A EP 07861028A EP 07861028 A EP07861028 A EP 07861028A EP 2128117 A2 EP2128117 A2 EP 2128117A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- modifier
- composition
- formula
- acid
- cooh
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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- 239000003607 modifier Substances 0.000 title claims abstract description 65
- 239000002360 explosive Substances 0.000 title claims description 99
- 239000000203 mixture Substances 0.000 claims abstract description 157
- 229920002678 cellulose Polymers 0.000 claims abstract description 25
- 239000001913 cellulose Substances 0.000 claims abstract description 25
- 150000001298 alcohols Chemical class 0.000 claims abstract description 18
- 150000003839 salts Chemical class 0.000 claims abstract description 15
- 150000002823 nitrates Chemical class 0.000 claims abstract description 10
- 150000001540 azides Chemical class 0.000 claims abstract description 6
- 150000007524 organic acids Chemical class 0.000 claims abstract description 6
- SFDJOSRHYKHMOK-UHFFFAOYSA-N nitramide Chemical class N[N+]([O-])=O SFDJOSRHYKHMOK-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 4
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 claims description 43
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 27
- 235000006408 oxalic acid Nutrition 0.000 claims description 15
- 229920001220 nitrocellulos Polymers 0.000 claims description 13
- 229910052757 nitrogen Inorganic materials 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 11
- 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 8
- AGUIVNYEYSCPNI-UHFFFAOYSA-N N-methyl-N-picrylnitramine Chemical compound [O-][N+](=O)N(C)C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O AGUIVNYEYSCPNI-UHFFFAOYSA-N 0.000 claims description 8
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 8
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 8
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 8
- -1 nitroisobutyl glycerinetrinitrate Chemical compound 0.000 claims description 7
- 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 6
- VBIXEXWLHSRNKB-UHFFFAOYSA-N ammonium oxalate Chemical compound [NH4+].[NH4+].[O-]C(=O)C([O-])=O VBIXEXWLHSRNKB-UHFFFAOYSA-N 0.000 claims description 5
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 claims description 5
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical class [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 claims description 5
- 125000004971 nitroalkyl group Chemical group 0.000 claims description 5
- 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 claims description 4
- JWQFKVGACKJIAV-UHFFFAOYSA-N 5-[(3-carboxy-4-hydroxyphenyl)methyl]-2-hydroxybenzoic acid Chemical compound C1=C(O)C(C(=O)O)=CC(CC=2C=C(C(O)=CC=2)C(O)=O)=C1 JWQFKVGACKJIAV-UHFFFAOYSA-N 0.000 claims description 4
- 239000005711 Benzoic acid Substances 0.000 claims description 4
- 244000248349 Citrus limon Species 0.000 claims description 4
- 235000005979 Citrus limon Nutrition 0.000 claims description 4
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 235000010233 benzoic acid Nutrition 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 235000013877 carbamide Nutrition 0.000 claims description 4
- LYAGTVMJGHTIDH-UHFFFAOYSA-N diethylene glycol dinitrate Chemical compound [O-][N+](=O)OCCOCCO[N+]([O-])=O LYAGTVMJGHTIDH-UHFFFAOYSA-N 0.000 claims description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- CFYAUGJHWXGWHI-UHFFFAOYSA-N n-methyl-2,4,6-trinitroaniline Chemical compound CNC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O CFYAUGJHWXGWHI-UHFFFAOYSA-N 0.000 claims description 4
- 150000005181 nitrobenzenes Chemical class 0.000 claims description 4
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 4
- 229960004889 salicylic acid Drugs 0.000 claims description 4
- 159000000000 sodium salts Chemical class 0.000 claims description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 4
- 239000000026 Pentaerythritol tetranitrate Substances 0.000 claims description 3
- IDNUEBSJWINEMI-UHFFFAOYSA-N ethyl nitrate Chemical compound CCO[N+]([O-])=O IDNUEBSJWINEMI-UHFFFAOYSA-N 0.000 claims description 3
- UQXKXGWGFRWILX-UHFFFAOYSA-N ethylene glycol dinitrate Chemical compound O=N(=O)OCCON(=O)=O UQXKXGWGFRWILX-UHFFFAOYSA-N 0.000 claims description 3
- DGMJZELBSFOPHH-KVTDHHQDSA-N mannite hexanitrate Chemical compound [O-][N+](=O)OC[C@@H](O[N+]([O-])=O)[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)CO[N+]([O-])=O DGMJZELBSFOPHH-KVTDHHQDSA-N 0.000 claims description 3
- 229960001765 mannitol hexanitrate Drugs 0.000 claims description 3
- LRMHVVPPGGOAJQ-UHFFFAOYSA-N methyl nitrate Chemical compound CO[N+]([O-])=O LRMHVVPPGGOAJQ-UHFFFAOYSA-N 0.000 claims description 3
- 229960004321 pentaerithrityl tetranitrate Drugs 0.000 claims description 3
- PSXCGTLGGVDWFU-UHFFFAOYSA-N propylene glycol dinitrate Chemical compound [O-][N+](=O)OC(C)CO[N+]([O-])=O PSXCGTLGGVDWFU-UHFFFAOYSA-N 0.000 claims description 3
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 3
- JCMBWDZBURXGMC-UHFFFAOYSA-N 1,3,6-trinitronaphthalene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=CC2=CC([N+](=O)[O-])=CC=C21 JCMBWDZBURXGMC-UHFFFAOYSA-N 0.000 claims description 2
- HJRJRUMKQCMYDL-UHFFFAOYSA-N 1-chloro-2,4,6-trinitrobenzene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=C(Cl)C([N+]([O-])=O)=C1 HJRJRUMKQCMYDL-UHFFFAOYSA-N 0.000 claims description 2
- IDCPFAYURAQKDZ-UHFFFAOYSA-N 1-nitroguanidine Chemical compound NC(=N)N[N+]([O-])=O IDCPFAYURAQKDZ-UHFFFAOYSA-N 0.000 claims description 2
- IAHOUQOWMXVMEH-UHFFFAOYSA-N 2,4,6-trinitroaniline Chemical compound NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O IAHOUQOWMXVMEH-UHFFFAOYSA-N 0.000 claims description 2
- GGGVOOMKPJYWDF-UHFFFAOYSA-N 2,4,6-trinitroxylene Chemical group CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(C)=C1[N+]([O-])=O GGGVOOMKPJYWDF-UHFFFAOYSA-N 0.000 claims description 2
- JHGWQSGWUPCKNT-UHFFFAOYSA-N 2-tert-butyl-4-methyl-1,3,5-trinitrobenzene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(C(C)(C)C)=C1[N+]([O-])=O JHGWQSGWUPCKNT-UHFFFAOYSA-N 0.000 claims description 2
- QTYYIZYAWHBAHQ-UHFFFAOYSA-N 3-(3-amino-2,4,6-trinitrophenyl)-2,4,6-trinitroaniline Chemical group NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(C=2C(=C(N)C(=CC=2[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O)=C1[N+]([O-])=O QTYYIZYAWHBAHQ-UHFFFAOYSA-N 0.000 claims description 2
- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 claims description 2
- UATJOMSPNYCXIX-UHFFFAOYSA-N Trinitrobenzene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 UATJOMSPNYCXIX-UHFFFAOYSA-N 0.000 claims description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
- 235000010338 boric acid Nutrition 0.000 claims description 2
- 229960002645 boric acid Drugs 0.000 claims description 2
- 229940105990 diglycerin Drugs 0.000 claims description 2
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims description 2
- XMWRWTSZNLOZFN-UHFFFAOYSA-N musk xylene Chemical compound CC1=C(N(=O)=O)C(C)=C(N(=O)=O)C(C(C)(C)C)=C1N(=O)=O XMWRWTSZNLOZFN-UHFFFAOYSA-N 0.000 claims description 2
- BUGRLMJGTJHURD-UHFFFAOYSA-N n-(2,4-dinitrophenyl)-n-methylnitramide Chemical compound [O-][N+](=O)N(C)C1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O BUGRLMJGTJHURD-UHFFFAOYSA-N 0.000 claims description 2
- IQEJEZOCXWJNKR-UHFFFAOYSA-N n-methyl-2,4-dinitroaniline Chemical compound CNC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O IQEJEZOCXWJNKR-UHFFFAOYSA-N 0.000 claims description 2
- QTXRAUAAUYMDLX-UHFFFAOYSA-N n-methyl-n-(4-nitrophenyl)nitramide Chemical compound [O-][N+](=O)N(C)C1=CC=C([N+]([O-])=O)C=C1 QTXRAUAAUYMDLX-UHFFFAOYSA-N 0.000 claims description 2
- 235000011007 phosphoric acid Nutrition 0.000 claims description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 2
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 claims description 2
- ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 claims description 2
- 229940039790 sodium oxalate Drugs 0.000 claims description 2
- IXHMHWIBCIYOAZ-UHFFFAOYSA-N styphnic acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1[N+]([O-])=O IXHMHWIBCIYOAZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000001384 succinic acid Substances 0.000 claims description 2
- JDFUJAMTCCQARF-UHFFFAOYSA-N tatb Chemical class NC1=C([N+]([O-])=O)C(N)=C([N+]([O-])=O)C(N)=C1[N+]([O-])=O JDFUJAMTCCQARF-UHFFFAOYSA-N 0.000 claims description 2
- 150000005190 tetranitrobenzenes Chemical class 0.000 claims description 2
- HSYGKEBJFKQOLE-UHFFFAOYSA-N 1,1,1-trinitroethane Chemical compound [O-][N+](=O)C(C)([N+]([O-])=O)[N+]([O-])=O HSYGKEBJFKQOLE-UHFFFAOYSA-N 0.000 claims 1
- LKKHEZBRRGJBGH-UHFFFAOYSA-N 1,1-dinitroethane Chemical compound [O-][N+](=O)C(C)[N+]([O-])=O LKKHEZBRRGJBGH-UHFFFAOYSA-N 0.000 claims 1
- UXGRXJVMQSSUGS-UHFFFAOYSA-N 1,2-dinitroethane Chemical compound [O-][N+](=O)CC[N+]([O-])=O UXGRXJVMQSSUGS-UHFFFAOYSA-N 0.000 claims 1
- LIPDUIOSIFXENT-UHFFFAOYSA-N 1,3,5-triazido-2,4,6-trinitrobenzene Chemical compound [O-][N+](=O)C1=C(N=[N+]=[N-])C([N+]([O-])=O)=C(N=[N+]=[N-])C([N+]([O-])=O)=C1N=[N+]=[N-] LIPDUIOSIFXENT-UHFFFAOYSA-N 0.000 claims 1
- FZAZPMLWYUKRAE-UHFFFAOYSA-N 2,4,6-trinitrobenzene-1,3-diamine Chemical compound NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(N)=C1[N+]([O-])=O FZAZPMLWYUKRAE-UHFFFAOYSA-N 0.000 claims 1
- FMXDVBRYDYFVGS-UHFFFAOYSA-N 2-methoxy-1,3,5-trinitrobenzene Chemical compound COC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O FMXDVBRYDYFVGS-UHFFFAOYSA-N 0.000 claims 1
- SLAMLWHELXOEJZ-UHFFFAOYSA-N 2-nitrobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1[N+]([O-])=O SLAMLWHELXOEJZ-UHFFFAOYSA-N 0.000 claims 1
- AFPHTEQTJZKQAQ-UHFFFAOYSA-N 3-nitrobenzoic acid Chemical compound OC(=O)C1=CC=CC([N+]([O-])=O)=C1 AFPHTEQTJZKQAQ-UHFFFAOYSA-N 0.000 claims 1
- OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- NYTOUQBROMCLBJ-UHFFFAOYSA-N Tetranitromethane Chemical compound [O-][N+](=O)C([N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O NYTOUQBROMCLBJ-UHFFFAOYSA-N 0.000 claims 1
- NSGHSKHYRLWFOD-UHFFFAOYSA-N [N+](=O)(O)[O-].[N+](=O)(O)[O-].[N+](=O)([O-])N.C(C)O.C(C)O Chemical compound [N+](=O)(O)[O-].[N+](=O)(O)[O-].[N+](=O)([O-])N.C(C)O.C(C)O NSGHSKHYRLWFOD-UHFFFAOYSA-N 0.000 claims 1
- CCAKQXWHJIKAST-UHFFFAOYSA-N hexanitroethane Chemical compound [O-][N+](=O)C([N+]([O-])=O)([N+]([O-])=O)C([N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O CCAKQXWHJIKAST-UHFFFAOYSA-N 0.000 claims 1
- CMUOJBJRZUHRMU-UHFFFAOYSA-N nitrourea Chemical compound NC(=O)N[N+]([O-])=O CMUOJBJRZUHRMU-UHFFFAOYSA-N 0.000 claims 1
- GEVPUGOOGXGPIO-UHFFFAOYSA-N oxalic acid;dihydrate Chemical compound O.O.OC(=O)C(O)=O GEVPUGOOGXGPIO-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 47
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract description 6
- 235000011187 glycerol Nutrition 0.000 abstract description 3
- 150000002009 diols Chemical class 0.000 abstract description 2
- 150000002334 glycols Chemical class 0.000 abstract description 2
- 150000002828 nitro derivatives Chemical class 0.000 abstract description 2
- 150000004072 triols Chemical class 0.000 abstract description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 1
- 230000035945 sensitivity Effects 0.000 description 29
- 235000019441 ethanol Nutrition 0.000 description 19
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 18
- 239000007789 gas Substances 0.000 description 17
- 238000000354 decomposition reaction Methods 0.000 description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 15
- 238000004880 explosion Methods 0.000 description 14
- 238000005474 detonation Methods 0.000 description 13
- 239000002131 composite material Substances 0.000 description 11
- 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 10
- 238000013329 compounding Methods 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 229940079938 nitrocellulose Drugs 0.000 description 10
- 239000000028 HMX Substances 0.000 description 8
- 239000000654 additive Substances 0.000 description 8
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- UZGLIIJVICEWHF-UHFFFAOYSA-N octogen Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 UZGLIIJVICEWHF-UHFFFAOYSA-N 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 230000007704 transition Effects 0.000 description 7
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 229910017604 nitric acid Inorganic materials 0.000 description 6
- 150000002913 oxalic acids Chemical class 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000004451 Ballistite Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 229910002651 NO3 Inorganic materials 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 150000002170 ethers Chemical class 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000006266 etherification reaction Methods 0.000 description 4
- 239000003721 gunpowder Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 229910001868 water Inorganic materials 0.000 description 4
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
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Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B23/00—Compositions characterised by non-explosive or non-thermic constituents
- C06B23/006—Stabilisers (e.g. thermal stabilisers)
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B23/00—Compositions characterised by non-explosive or non-thermic constituents
- C06B23/005—Desensitisers, phlegmatisers
Definitions
- the proposed invention relates to modifiers from the range of organic and inorganic compositions, capable to modify their thermodynamic parameters, physical, chemical, biochemical properties for explosives, including gas generating compositions, rocket fuels and gunpowders based thereon.
- Glycerine trinitrate in the pure state is not applied because of its extreme instability, and, during its decomposition not only enormous quantity of energy is liberated as heat and huge volume of the heated gases: nitrogen, water, carbon dioxide, but also oxygen in free condition [1, 2] which may be used for amplification for explosive action of glycerine trinitrate in its mix with combustible materials including ethers of nitric acid of monoatomic, diatomic, triatomic and multinuclear alcohols, as well as cellulose [1-5], thus it is possible to obtain dynamites with active and inactive weight [1], for example, with fossil meal, a special kind of silica (porous SiO 2 , kieselguhr) [1-5].
- glycerine trinitrate other nitrates of alcohols became important as explosives, that is complex complete or/and incomplete ethers of alcohols and nitric acid, for example, methyl nitrate, ethyl nitrate [4], ethylene glycol dinitrate [2,4], propylene glycol dinitrate [2], mannitol hexanitrate, pentaerythritol tetranitrate [1] and so on [6, 7, 8]. They are safer to operate as compared to glycerine trinitrate, but as well as the latter they are also unsuitable for use when shooting with fire-arms.
- trinitro cellulose or pyroxylin where all the three hydroxyls are replaced by the residues of nitric acid [1-5], as well as glycerine trinitrate is a detonating explosive featuring high energy and it is applied as shattering explosive in blasting works, but it is not applied when shooting from gun and rocket weapon as the shattering explosion would break the installation before the projectile would come to movement [1-5].
- trinitro cellulose in gun systems it is necessary to slow down the speed of its combustion so as to gradually accrue the pressure of formed gases to set a projectile in motion (to push it out) [1-5].
- trinitro cellulose For reducing the speed of its combustion the trinitro cellulose is being gelled using various solvents, for example such as acetone, vinegar amyl ether and others [1], i.e. trinitrate of cellulose swells and forms dense jellylike mass; such a mass is used for pressing tapes of various thickness and sizes which after drying may be applied as a smokeless gunpowder. They are burning down more slowly than trinitrate of cellulose that enables to use them for shooting from gun and rocket installations. For obtaining a weapon smokeless gunpowder they are being cut to fine slices.
- solvents for example such as acetone, vinegar amyl ether and others [1]
- trinitrate of cellulose swells and forms dense jellylike mass
- such a mass is used for pressing tapes of various thickness and sizes which after drying may be applied as a smokeless gunpowder. They are burning down more slowly than trinitrate of cellulose that enables to use them for shooting from gun and rocket installations. For obtaining
- trinitrate of cellulose is also being gelled by using glycerine trinitrate thus the formed mass represents a special kind of dynamite also used in blasting works under the name "blasting gelatin” [1].
- the properties of trinitrate of cellulose are similar to those of similar complete or incomplete ethers formed during interaction (etherification) of our proposed corresponding alcohols with a mix of nitric and sulfuric acids
- the principles of the approach to the decision of tasks for purposeful modification of thermodynamic (thermochemical) parameters and stability influences negatively influencing the properties and quality of trinitrate of cellulose are authentic, as well as the substances (compositions) applied (used) as universal modifiers of new composite structures of compoundings of power systems of driving force based thereon.
- smokeless gunpowders are produced on the basis of nitrates of cellulose in structure with various softeners.
- smokeless gunpowders on the basis of glycerine trinitrate (ballistites) and pyroxylin [the Soviet encyclopaedic dictionary.-M.: Soviet encyclopedia, 1983, p.119 ].
- Smokeless gunpowders, both artillery ballistite and pyroxylin, and ballistite rocket firm fuel differ the big variety on ra ap THO-mass parameters (characteristics), structure, sensitivity a various sort to mechanical influences, power parameters, speed of burning, sensitivity a detonation pulse.
- liquid explosives such as glycerine trinitrate or compositions (structures, compoundings) based thereon
- high-energy substances in particular glycerine trinitrate
- compositions are constant objects for creating on the basis thereon explosive compositions for various purpose.
- retarding additives are used (applied).
- tri-nitro-glycerin explosive compositions substances, compoundings
- special-purpose designations including industrial (commercial) explosives, such as pobedits, detonites and similar compounds are created.
- these compositions (compounds) feature rather low sensitivity to mechanical influences due to low contents (approximately 10 %) of glycerine trinitrate and at the same time, and for the same reason they feature low energy characteristic (response).
- compositions on the basis of glycerine trinitrate
- Patent US 4011114, CI . C 06 B 45/10, 1976 These compositions (compoundings) feature rather high sensitivity to mechanical influences and low energy properties because of low (small) oxygen factor.
- Use (application) of trimethylolethane trinitrate as a retarder for glycerine trinitrate.
- Another gas generating composition for fire extinguishers contains in mass.% dibutil phthalate (17), acetate of cellulose (7,6), N-methyl-p-nitroaniline (1), nitrate of cellulose (30,4), trinitrate of pentaeritrit (37), ethyl centralite (2), tin oxides (5) while the temperature of its burning makes 1700°K. [Patent US 3639183, Cl . C 06 D 5/06, 1972].
- the purpose of improvement of such compositions is lowering the sensitivity to various mechanical influences and lowering the temperature of burning; and the main components of such compositions remain almost without qualitative and quantitative changes.
- the engineering problem of the invention consists in creating a universal modifier for explosives from a range of composite complete or incomplete nitrates of monoatomic, diatomic, triatomic or multinuclear alcohols, nitrocelluloses, nitroamines, azides, nitrobenzenes or nitroalkanes; introducing such a modifier in these explosives allows to modify their thermodynamic parameters, physical, chemical, biochemical properties and to create on the basis of these explosives, with the introduced modifiers, explosive and unexplosive composite compounds having liquid (consistent), heterogeneous or solid aggregate state depending on objects in view (tasks) with required properties that may vary, by varying the ratio of components included in the composition.
- the technical result of the invention is the inhibition of premature decomposition of explosives (compounds) at all the initial stages of development of this process, with its subsequent initiation (activation) as a result of smooth and fast growth (increase) of temperature thus leading to explosive decomposition or burning depending on sufficiency surplus of oxygen in the system, both due to oxygen-containing compounds (substances), and as a result of emission of oxygen in a pure state when decomposing the substances (compounds) included in explosive composition, i.e. controlling the rate of their decomposition, as well as decrease in sensitivity of explosives to various mechanical influences, improvement of the degree of compression.
- compositions have, basically, rather low temperature of decomposition and rather high temperature of ignition, thus, a part of thermal energy will be spent for decomposing these substances when introducing them into the specified explosives, thus there will be a decrease of general (total) temperature of formed gases with simultaneous increase in their volumes and there will be a proportional development of pressure due to gases formed as a result of decomposition and-or burning of these compositions.
- the explosives from the range of complex complete or incomplete nitrates of monoatomic, diatomic, triatomic or multinuclear alcohols, nitrocelluloses, nitroamines, nitroanilines, azides, nitrobenzenes or nitroalkanes, where it is offered to introduce the above modifiers, may be the following explosives:
- compositions do not limit the possible assortment of various other explosives (copositions) that in combination (mix) with our proposed compositions (substances) from between organic, inorganic acids and their salts or other of substances (compositions), featuring similar properties and used as universal modifiers, may also similarly (purposefully) influence various parameters and properties of new energy systems of driving force created on their basis with characteristics required for any specific purpose, where, the same explosive composition may feature different speed of decomposition depending on the way (method) of its activation, and may also show the properties of simple burning not passing to detonation or brisances, i.e.
- compositions As the operating principle of our offered modifiers in various composite structures of compounds for the specified classes of explosives (compositions) is essentially the same, and it consists in that these modifiers and substances (compositions) having similar properties under certain conditions may decay with emitting gaseous products, and in presence of enough of oxygen in the system may occur not only their decomposition, but also burning or a combination of these processes, thus there may be a thermodynamic (thermochemical) effect of significant decrease in temperature and increase in volume of the formed gases, and incidental proportional development of certain pressure [and the effect of decrease in temperature of gases is most pronounced in case when the compositions (substances) having the temperature of decomposition that is lower or coincides with the temperature of ignition are used (are applied) as modifiers], our approach to creating explosive and unexplosive energy systems of driving force with the properties set depending on the object in view is general and universal for all such systems.
- thermodynamic thermochemical
- the modifier for our offered explosives may be used in case of the ratio modifier/explosive equal to (0,1-99,9 : (99,9-0,1).
- FIG. 1 and Fig. 2 there are the diagrams of decomposition of mixes of oxalic acids (crystalline hydrate) with glycerine trinitrate in mass ratio 1:2 and 1:5 accordingly; it was been found that introducting oxalic acids (crystalline hydrate) does not worsen the heat-resistant characteristics of glycerine trinitrate. It is also determined, that the composition is not susceptible to transition of burning to explosion or detonation.
- FIG. 3 there is a diagram of decomposition of a mix of ammonium oxalate (crystalline hydrate) with glycerine trinitrate in mass ratio 1:1 accordingly, it was been found that introducing ammonium oxalate (crystalline hydrate) does not worsen the heat-resistant characteristics of glycerine trinitrate, but also renders inhibitory action on its autocatalytic decomposition. It is also determined, that the composition is not sucseptible to transition of burning to explosion or detonation.
- the mixes were prepared similarly to those of Example 1.
- Thematic examples are mixes of oxalic acids (crystalline hydrate) with glycerine trinitrate, thus the mixes prepared in mass ratio: composition No1 - 1:5, composition No2 - 1:2, composition No3 - 1:1, composition No4 - 2:1 accordingly, have been tested for explosive characteristics using a Kast's impact machine OST B 84-892-74 (Sensitivity impact using an impact machine at the bottom limit with instr. No1 and instr. No2) and the following results are received:
- compositions have been tested for sensitivity to shock-free friction at the bottom limit (OST B 84-894-74) at a speed of disk rotation (friction) of 520 rev/min.
- the tests were carried out at a temperature of 18°C.
- compositions have been tested for sensitivity to friction at a shock shift at the bottom limit (OST B 84-895-83).
- gelatinating (swelling) and polymeric compositions (substances) were used, such as pyroxylin, colloxylin and other compositions in monobasic and bibasic composite materials with our offered modifiers.
- the product is plastic, it is susceptible to molding, there is also an expressed influence of the modifier on the speed of burning and temperature of the obtained gases.
- the thematic example are also the obtained compositions of pyroxylin with salt of methylenedisalicylic acid.
- the stability of gunpowders made 3,5 to 4,5 kPa, at a norm of 8 kPa.
- diammonium salt of methylenedisalicylic acid up to 20% of mass. essential decrease in temperature of the formed gases down by 700-800 °K was marked, while maintaining acceptable power of gunpowders.
- compositions of pyroxylin with lemon salt may also servea thematic example, because when introducing it up to 0,5 % mass., the stability of gunpowders made 3,5-4,5 kPa, at a norm of 8 kPa. When introducing the lemon salt up to 20 % mass., the obtained compositions had the power of gunpowder comparable to the normal one at a level of 1030 to 1060 kJ/kg.
- thermodynamic calculated values of obtained compositions which had good convergence of results and completely confirmed the experimental data and the Claims.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2006136245/02A RU2318789C1 (ru) | 2006-10-16 | 2006-10-16 | Модификатор взрывчатых веществ |
PCT/RU2007/000556 WO2008048146A2 (fr) | 2006-10-16 | 2007-10-12 | Modificateur pour substances explosives |
Publications (2)
Publication Number | Publication Date |
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EP2128117A2 true EP2128117A2 (de) | 2009-12-02 |
EP2128117A4 EP2128117A4 (de) | 2013-10-30 |
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EP07861028.4A Withdrawn EP2128117A4 (de) | 2006-10-16 | 2007-10-12 | Modifizierungsmittel für sprengstoffe |
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US (2) | US20100096050A1 (de) |
EP (1) | EP2128117A4 (de) |
JP (1) | JP2010506821A (de) |
RU (1) | RU2318789C1 (de) |
WO (1) | WO2008048146A2 (de) |
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CN114045039B (zh) * | 2021-12-09 | 2022-10-04 | 湖南卫航科技有限公司 | 一种炸药模拟物及其制备方法、应用 |
CN115709075A (zh) * | 2022-11-15 | 2023-02-24 | 西安近代化学研究所 | 一种纳米二氧化锡负载单原子燃烧催化剂及其制备方法 |
CN116283452A (zh) * | 2023-03-03 | 2023-06-23 | 西南科技大学 | 基于pickering乳液法制备炸药/HNS核壳结构球形复合物的方法 |
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2006
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-
2007
- 2007-10-12 US US12/445,387 patent/US20100096050A1/en not_active Abandoned
- 2007-10-12 EP EP07861028.4A patent/EP2128117A4/de not_active Withdrawn
- 2007-10-12 JP JP2009533273A patent/JP2010506821A/ja active Pending
- 2007-10-12 WO PCT/RU2007/000556 patent/WO2008048146A2/ru active Application Filing
-
2012
- 2012-05-16 US US13/473,369 patent/US20120291931A1/en not_active Abandoned
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Also Published As
Publication number | Publication date |
---|---|
WO2008048146A2 (fr) | 2008-04-24 |
WO2008048146A3 (fr) | 2008-06-19 |
JP2010506821A (ja) | 2010-03-04 |
US20100096050A1 (en) | 2010-04-22 |
RU2318789C1 (ru) | 2008-03-10 |
US20120291931A1 (en) | 2012-11-22 |
EP2128117A4 (de) | 2013-10-30 |
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