JP2010506821A - 爆薬用調整剤 - Google Patents
爆薬用調整剤 Download PDFInfo
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- JP2010506821A JP2010506821A JP2009533273A JP2009533273A JP2010506821A JP 2010506821 A JP2010506821 A JP 2010506821A JP 2009533273 A JP2009533273 A JP 2009533273A JP 2009533273 A JP2009533273 A JP 2009533273A JP 2010506821 A JP2010506821 A JP 2010506821A
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- 239000002360 explosive Substances 0.000 title claims abstract description 108
- 239000000203 mixture Substances 0.000 claims abstract description 177
- 239000003607 modifier Substances 0.000 claims abstract description 44
- 229920002678 cellulose Polymers 0.000 claims abstract description 16
- 239000001913 cellulose Substances 0.000 claims abstract description 16
- 150000003839 salts Chemical class 0.000 claims abstract description 14
- 229910002651 NO3 Inorganic materials 0.000 claims abstract description 8
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims abstract description 6
- 150000001540 azides Chemical class 0.000 claims abstract description 5
- SFDJOSRHYKHMOK-UHFFFAOYSA-N nitramide Chemical compound N[N+]([O-])=O SFDJOSRHYKHMOK-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000007524 organic acids Chemical class 0.000 claims abstract description 5
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 51
- 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 47
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 31
- 235000006408 oxalic acid Nutrition 0.000 claims description 17
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000020 Nitrocellulose Substances 0.000 claims description 9
- 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 claims description 9
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- 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
- 239000004202 carbamide Substances 0.000 claims description 4
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- 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
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- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
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- 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
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- 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
- ORFRLGIDGMPZRH-UHFFFAOYSA-N (5-methyl-3-nitro-1,2-dinitrooxyhexan-3-yl) nitrate Chemical compound CC(C)CC(O[N+]([O-])=O)([N+]([O-])=O)C(O[N+]([O-])=O)CO[N+]([O-])=O ORFRLGIDGMPZRH-UHFFFAOYSA-N 0.000 claims description 2
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- 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
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- SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- 239000000026 Pentaerythritol tetranitrate Substances 0.000 claims description 2
- 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 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
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- CMUOJBJRZUHRMU-UHFFFAOYSA-N nitrourea Chemical compound NC(=O)N[N+]([O-])=O CMUOJBJRZUHRMU-UHFFFAOYSA-N 0.000 claims description 2
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- 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
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- C06B23/006—Stabilisers (e.g. thermal stabilisers)
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- C—CHEMISTRY; METALLURGY
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- 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
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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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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RU2247102C1 (ru) * | 2003-08-25 | 2005-02-27 | Федеральное государственное унитарное предприятие Федеральный научно-производственный центр "Алтай" | Взрывчатое вещество |
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RU2244703C1 (ru) | 2003-12-02 | 2005-01-20 | Инновационный фонд "Развития и взаимосвязи культур, наук, образований, религий, обществ, стран" ("РиВКНОРОС") | Стабилизатор химической стойкости пороха, твердого ракетного топлива и газогенерирующего состава на основе нитроцеллюлозы и способ их обработки |
US8092623B1 (en) * | 2006-01-31 | 2012-01-10 | The United States Of America As Represented By The Secretary Of The Navy | Igniter composition, and related methods and devices |
-
2006
- 2006-10-16 RU RU2006136245/02A patent/RU2318789C1/ru not_active IP Right Cessation
-
2007
- 2007-10-12 US US12/445,387 patent/US20100096050A1/en not_active Abandoned
- 2007-10-12 JP JP2009533273A patent/JP2010506821A/ja active Pending
- 2007-10-12 WO PCT/RU2007/000556 patent/WO2008048146A2/ru active Application Filing
- 2007-10-12 EP EP07861028.4A patent/EP2128117A4/en not_active Withdrawn
-
2012
- 2012-05-16 US US13/473,369 patent/US20120291931A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
RU2318789C1 (ru) | 2008-03-10 |
EP2128117A2 (en) | 2009-12-02 |
US20100096050A1 (en) | 2010-04-22 |
WO2008048146A3 (fr) | 2008-06-19 |
EP2128117A4 (en) | 2013-10-30 |
WO2008048146A2 (fr) | 2008-04-24 |
US20120291931A1 (en) | 2012-11-22 |
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