SE500687C2 - Energetiska material - Google Patents

Energetiska material

Info

Publication number: SE500687C2
Authority: SE; Sweden
Prior art keywords: component; weight; composition according; compound; composition
Prior art date: 1986-07-04

Application number

SE8801944A

Other languages

English (en)

Swedish (sv)

Other versions

SE8801944D0 (sv

SE8801944L (sv

Inventor

Ronald Benjamin Holt

John Charles Martin Phillips

Original Assignee

Royal Ordnance Plc

Priority date (The priority date 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 date listed.)

1986-07-04

Filing date

1988-05-25

Publication date

1994-08-08

1986-07-04 Priority claimed from GB868616322A external-priority patent/GB8616322D0/en

1988-05-25 Application filed by Royal Ordnance Plc filed Critical Royal Ordnance Plc

1988-05-25 Publication of SE8801944D0 publication Critical patent/SE8801944D0/xx

1991-09-06 Publication of SE8801944L publication Critical patent/SE8801944L/

1994-08-08 Publication of SE500687C2 publication Critical patent/SE500687C2/sv

Links

239000000463 material Substances 0.000 title claims description 17
239000000203 mixture Substances 0.000 claims abstract description 86
150000001875 compounds Chemical class 0.000 claims abstract description 27
239000000020 Nitrocellulose Substances 0.000 claims abstract description 23
229920001220 nitrocellulos Polymers 0.000 claims abstract description 23
239000011230 binding agent Substances 0.000 claims abstract description 14
239000004014 plasticizer Substances 0.000 claims abstract description 13
-1 nitramine compound Chemical class 0.000 claims abstract description 8
229920002678 cellulose Polymers 0.000 claims abstract description 6
BSPUVYFGURDFHE-UHFFFAOYSA-N Nitramine Natural products CC1C(O)CCC2CCCNC12 BSPUVYFGURDFHE-UHFFFAOYSA-N 0.000 claims abstract description 5
239000000945 filler Substances 0.000 claims abstract description 5
POCJOGNVFHPZNS-UHFFFAOYSA-N isonitramine Natural products OC1CCCCC11CNCCC1 POCJOGNVFHPZNS-UHFFFAOYSA-N 0.000 claims abstract description 5
239000003380 propellant Substances 0.000 claims description 18
229920006217 cellulose acetate butyrate Polymers 0.000 claims description 17
150000002828 nitro derivatives Chemical class 0.000 claims description 9
POCJOGNVFHPZNS-ZJUUUORDSA-N (6S,7R)-2-azaspiro[5.5]undecan-7-ol Chemical class O[C@@H]1CCCC[C@]11CNCCC1 POCJOGNVFHPZNS-ZJUUUORDSA-N 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 6
PQSWCVYWEGIBPY-UHFFFAOYSA-N 2,2-dinitroethylbenzene Chemical class [O-][N+](=O)C([N+]([O-])=O)CC1=CC=CC=C1 PQSWCVYWEGIBPY-UHFFFAOYSA-N 0.000 claims description 5
125000003118 aryl group Chemical group 0.000 claims description 5
KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 claims description 4
RMBFBMJGBANMMK-UHFFFAOYSA-N 2,4-dinitrotoluene Chemical compound CC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O RMBFBMJGBANMMK-UHFFFAOYSA-N 0.000 claims description 4
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical class CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 4
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 4
150000005224 alkoxybenzenes Chemical class 0.000 claims description 4
OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000007788 liquid Substances 0.000 claims description 4
ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 claims description 4
125000000547 substituted alkyl group Chemical group 0.000 claims description 4
XUUSVHGZGPBZLS-UHFFFAOYSA-N 1,3-dimethyl-2,4-dinitrobenzene Chemical group CC1=CC=C([N+]([O-])=O)C(C)=C1[N+]([O-])=O XUUSVHGZGPBZLS-UHFFFAOYSA-N 0.000 claims description 3
XOXVLXUOMLQTLM-UHFFFAOYSA-N 1-ethyl-2,3,4-trinitrobenzene Chemical compound CCC1=CC=C([N+]([O-])=O)C([N+]([O-])=O)=C1[N+]([O-])=O XOXVLXUOMLQTLM-UHFFFAOYSA-N 0.000 claims description 3
ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 claims description 3
239000000028 HMX Substances 0.000 claims description 3
125000002950 monocyclic group Chemical group 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 claims description 2
GHLOZOFSZVNFMD-UHFFFAOYSA-N 3,3-dinitropropylbenzene Chemical class [O-][N+](=O)C([N+]([O-])=O)CCC1=CC=CC=C1 GHLOZOFSZVNFMD-UHFFFAOYSA-N 0.000 claims description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 claims description 2
125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
150000003613 toluenes Chemical class 0.000 claims description 2
150000005186 trinitrobenzenes Chemical class 0.000 claims description 2
239000008096 xylene Substances 0.000 claims description 2
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 2
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 claims 2
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 claims 1
PZIMIYVOZBTARW-UHFFFAOYSA-N centralite Chemical compound C=1C=CC=CC=1N(CC)C(=O)N(CC)C1=CC=CC=C1 PZIMIYVOZBTARW-UHFFFAOYSA-N 0.000 abstract description 6
239000000306 component Substances 0.000 description 117
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 7
239000004202 carbamide Substances 0.000 description 7
239000000654 additive Substances 0.000 description 5
RPQSKHWNIKZEAI-UHFFFAOYSA-N 1-ethyl-2,4-dinitrobenzene Chemical compound CCC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O RPQSKHWNIKZEAI-UHFFFAOYSA-N 0.000 description 4
SWASTJCUMFALOW-UHFFFAOYSA-N 2-ethyl-1,3-dinitrobenzene Chemical compound CCC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O SWASTJCUMFALOW-UHFFFAOYSA-N 0.000 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 description 4
229920002301 cellulose acetate Polymers 0.000 description 4
239000008187 granular material Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
ZITQIEGKEPOOPD-UHFFFAOYSA-N 1,2,4-trinitro-5-propan-2-ylbenzene Chemical compound CC(C)C1=CC([N+]([O-])=O)=C([N+]([O-])=O)C=C1[N+]([O-])=O ZITQIEGKEPOOPD-UHFFFAOYSA-N 0.000 description 3
PVLUMVBVQMIJPD-UHFFFAOYSA-N 1,3-dinitro-2-propan-2-ylbenzene Chemical compound CC(C)C1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O PVLUMVBVQMIJPD-UHFFFAOYSA-N 0.000 description 3
IDCPFAYURAQKDZ-UHFFFAOYSA-N 1-nitroguanidine Chemical compound NC(=N)N[N+]([O-])=O IDCPFAYURAQKDZ-UHFFFAOYSA-N 0.000 description 3
BAWGGSYXBBWRAO-UHFFFAOYSA-N 2,4-dinitro-1-propan-2-ylbenzene Chemical compound CC(C)C1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O BAWGGSYXBBWRAO-UHFFFAOYSA-N 0.000 description 3
VDKWJWFQFPWXFC-UHFFFAOYSA-N 2-ethyl-1,3,5-trinitrobenzene Chemical compound CCC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O VDKWJWFQFPWXFC-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
239000001913 cellulose Substances 0.000 description 3
238000002485 combustion reaction Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
238000001125 extrusion Methods 0.000 description 3
239000004744 fabric Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
QUAMCNNWODGSJA-UHFFFAOYSA-N 1,1-dinitrooxybutyl nitrate Chemical compound CCCC(O[N+]([O-])=O)(O[N+]([O-])=O)O[N+]([O-])=O QUAMCNNWODGSJA-UHFFFAOYSA-N 0.000 description 2
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
XTRDKALNCIHHNI-UHFFFAOYSA-N 2,6-dinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O XTRDKALNCIHHNI-UHFFFAOYSA-N 0.000 description 2
AQDKZPFDOWHRDZ-UHFFFAOYSA-N 2-methyl-6-nitrophenol Chemical compound CC1=CC=CC([N+]([O-])=O)=C1O AQDKZPFDOWHRDZ-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
239000000006 Nitroglycerin Substances 0.000 description 2
PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
150000004996 alkyl benzenes Chemical class 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
239000003063 flame retardant Substances 0.000 description 2
229960003711 glyceryl trinitrate Drugs 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
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239000004814 polyurethane Substances 0.000 description 2
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 2
235000021286 stilbenes Nutrition 0.000 description 2
URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 2
239000000015 trinitrotoluene Substances 0.000 description 2
PNBOBRKDXRJMTL-UHFFFAOYSA-N (2-nitrophenyl) benzoate Chemical compound [O-][N+](=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1 PNBOBRKDXRJMTL-UHFFFAOYSA-N 0.000 description 1
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RDLIBIDNLZPAQD-UHFFFAOYSA-N 1,2,4-butanetriol trinitrate Chemical compound [O-][N+](=O)OCCC(O[N+]([O-])=O)CO[N+]([O-])=O RDLIBIDNLZPAQD-UHFFFAOYSA-N 0.000 description 1
QCZUVZZGFJABPY-UHFFFAOYSA-N 1,2,5-trimethyl-3-nitrobenzene Chemical compound CC1=CC(C)=C(C)C([N+]([O-])=O)=C1 QCZUVZZGFJABPY-UHFFFAOYSA-N 0.000 description 1
QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 1
DWVNLBRNGAANPI-UHFFFAOYSA-N 1,2-dimethoxy-3-nitrobenzene Chemical compound COC1=CC=CC([N+]([O-])=O)=C1OC DWVNLBRNGAANPI-UHFFFAOYSA-N 0.000 description 1
YFWBUVZWCBFSQN-UHFFFAOYSA-N 1,2-dimethoxy-4-nitrobenzene Chemical compound COC1=CC=C([N+]([O-])=O)C=C1OC YFWBUVZWCBFSQN-UHFFFAOYSA-N 0.000 description 1
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FVHAWXWFPBPFOS-UHFFFAOYSA-N 1,2-dimethyl-3-nitrobenzene Chemical compound CC1=CC=CC([N+]([O-])=O)=C1C FVHAWXWFPBPFOS-UHFFFAOYSA-N 0.000 description 1
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SCEKDQTVGHRSNS-UHFFFAOYSA-N 1,3,5-trimethyl-2-nitrobenzene Chemical compound CC1=CC(C)=C([N+]([O-])=O)C(C)=C1 SCEKDQTVGHRSNS-UHFFFAOYSA-N 0.000 description 1
MVBXGGHFJZBKFJ-UHFFFAOYSA-N 1,3-dimethoxy-2-nitrobenzene Chemical compound COC1=CC=CC(OC)=C1[N+]([O-])=O MVBXGGHFJZBKFJ-UHFFFAOYSA-N 0.000 description 1
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BYFNZOKBMZKTSC-UHFFFAOYSA-N 1,3-dimethyl-5-nitrobenzene Chemical compound CC1=CC(C)=CC([N+]([O-])=O)=C1 BYFNZOKBMZKTSC-UHFFFAOYSA-N 0.000 description 1
WDCYWAQPCXBPJA-UHFFFAOYSA-N 1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1 WDCYWAQPCXBPJA-UHFFFAOYSA-N 0.000 description 1
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ZQXWPHXDXHONFS-UHFFFAOYSA-N 1-(2,2-dinitropropoxymethoxy)-2,2-dinitropropane Chemical compound [O-][N+](=O)C([N+]([O-])=O)(C)COCOCC(C)([N+]([O-])=O)[N+]([O-])=O ZQXWPHXDXHONFS-UHFFFAOYSA-N 0.000 description 1
VOCGCNMEKJPLQQ-UHFFFAOYSA-N 1-(2-methylpropoxy)-2-nitrobenzene Chemical compound CC(C)COC1=CC=CC=C1[N+]([O-])=O VOCGCNMEKJPLQQ-UHFFFAOYSA-N 0.000 description 1
XGLGESCVNJSAQY-UHFFFAOYSA-N 1-ethoxy-2-nitrobenzene Chemical compound CCOC1=CC=CC=C1[N+]([O-])=O XGLGESCVNJSAQY-UHFFFAOYSA-N 0.000 description 1
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NWPKEYHUZKMWKJ-UHFFFAOYSA-N 1-ethoxy-4-nitrobenzene Chemical compound CCOC1=CC=C([N+]([O-])=O)C=C1 NWPKEYHUZKMWKJ-UHFFFAOYSA-N 0.000 description 1
RXAKLPGKSXJZEF-UHFFFAOYSA-N 1-ethyl-3-nitrobenzene Chemical compound CCC1=CC=CC([N+]([O-])=O)=C1 RXAKLPGKSXJZEF-UHFFFAOYSA-N 0.000 description 1
RESTWAHJFMZUIZ-UHFFFAOYSA-N 1-ethyl-4-nitrobenzene Chemical compound CCC1=CC=C([N+]([O-])=O)C=C1 RESTWAHJFMZUIZ-UHFFFAOYSA-N 0.000 description 1
WSZPRLKJOJINEP-UHFFFAOYSA-N 1-fluoro-2-[(2-fluoro-2,2-dinitroethoxy)methoxy]-1,1-dinitroethane Chemical compound [O-][N+](=O)C(F)([N+]([O-])=O)COCOCC(F)([N+]([O-])=O)[N+]([O-])=O WSZPRLKJOJINEP-UHFFFAOYSA-N 0.000 description 1
OTMLGCBMOMNGCV-UHFFFAOYSA-N 1-methoxy-3,5-dinitrobenzene Chemical compound COC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 OTMLGCBMOMNGCV-UHFFFAOYSA-N 0.000 description 1
DRKFWQDBPGTSOO-UHFFFAOYSA-N 1-methyl-2-nitro-4-propan-2-ylbenzene Chemical compound CC(C)C1=CC=C(C)C([N+]([O-])=O)=C1 DRKFWQDBPGTSOO-UHFFFAOYSA-N 0.000 description 1
BSMKYQUHXQAVKG-UHFFFAOYSA-N 1-nitro-2-propan-2-ylbenzene Chemical compound CC(C)C1=CC=CC=C1[N+]([O-])=O BSMKYQUHXQAVKG-UHFFFAOYSA-N 0.000 description 1
JXMYUMNAEKRMIP-UHFFFAOYSA-N 1-nitro-4-propan-2-ylbenzene Chemical compound CC(C)C1=CC=C([N+]([O-])=O)C=C1 JXMYUMNAEKRMIP-UHFFFAOYSA-N 0.000 description 1
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
BJAMBVUZPFZLHT-UHFFFAOYSA-N 2,3-dimethyl-1,4-dinitrobenzene Chemical compound CC1=C(C)C([N+]([O-])=O)=CC=C1[N+]([O-])=O BJAMBVUZPFZLHT-UHFFFAOYSA-N 0.000 description 1
XXWIYOBCHKCWNT-UHFFFAOYSA-N 2,4-dimethoxy-1-nitrobenzene Chemical compound COC1=CC=C([N+]([O-])=O)C(OC)=C1 XXWIYOBCHKCWNT-UHFFFAOYSA-N 0.000 description 1
MCRYBELDVGNCFW-UHFFFAOYSA-N 2,4-dimethyl-3-nitroaniline Chemical compound CC1=CC=C(N)C(C)=C1[N+]([O-])=O MCRYBELDVGNCFW-UHFFFAOYSA-N 0.000 description 1
VSRYYONYIUUFFY-UHFFFAOYSA-N 2,4-dimethyl-6-nitroaniline Chemical compound CC1=CC(C)=C(N)C([N+]([O-])=O)=C1 VSRYYONYIUUFFY-UHFFFAOYSA-N 0.000 description 1
KJRCHILWKQLEBC-UHFFFAOYSA-N 2,4-dimethyl-6-nitrophenol Chemical compound CC1=CC(C)=C(O)C([N+]([O-])=O)=C1 KJRCHILWKQLEBC-UHFFFAOYSA-N 0.000 description 1
CVYZVNVPQRKDLW-UHFFFAOYSA-N 2,4-dinitroanisole Chemical compound COC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O CVYZVNVPQRKDLW-UHFFFAOYSA-N 0.000 description 1
YSOKMOXAGMIZFZ-UHFFFAOYSA-N 2,4-dinitrophenetole Chemical compound CCOC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O YSOKMOXAGMIZFZ-UHFFFAOYSA-N 0.000 description 1
HHBUAAXHXWSZAG-UHFFFAOYSA-N 2,5-dimethyl-3-nitrophenol Chemical compound CC1=CC(O)=C(C)C([N+]([O-])=O)=C1 HHBUAAXHXWSZAG-UHFFFAOYSA-N 0.000 description 1
LDFJDBAOBVUXMQ-UHFFFAOYSA-N 2,6-dimethyl-3-nitroaniline Chemical compound CC1=CC=C([N+]([O-])=O)C(C)=C1N LDFJDBAOBVUXMQ-UHFFFAOYSA-N 0.000 description 1
TZASZCQVZPLXHP-UHFFFAOYSA-N 2,6-dimethyl-3-nitrophenol Chemical compound CC1=CC=C([N+]([O-])=O)C(C)=C1O TZASZCQVZPLXHP-UHFFFAOYSA-N 0.000 description 1
HOYRZHJJAHRMLL-UHFFFAOYSA-N 2,6-dinitro-p-cresol Chemical compound CC1=CC([N+]([O-])=O)=C(O)C([N+]([O-])=O)=C1 HOYRZHJJAHRMLL-UHFFFAOYSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
JSOGDEOQBIUNTR-UHFFFAOYSA-N 2-(azidomethyl)oxirane Chemical compound [N-]=[N+]=NCC1CO1 JSOGDEOQBIUNTR-UHFFFAOYSA-N 0.000 description 1
TXPURXMTKXRAMV-UHFFFAOYSA-N 2-[2-[2-(2-nitrooxyethoxy)ethoxy]ethoxy]ethyl nitrate Chemical compound [O-][N+](=O)OCCOCCOCCOCCO[N+]([O-])=O TXPURXMTKXRAMV-UHFFFAOYSA-N 0.000 description 1
LFQOLCFZVKRNMD-UHFFFAOYSA-N 2-ethoxy-1,3-dinitrobenzene Chemical compound CCOC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O LFQOLCFZVKRNMD-UHFFFAOYSA-N 0.000 description 1
HYQXQXJWUMOPKU-UHFFFAOYSA-N 2-ethoxy-1,4-dinitrobenzene Chemical compound CCOC1=CC([N+]([O-])=O)=CC=C1[N+]([O-])=O HYQXQXJWUMOPKU-UHFFFAOYSA-N 0.000 description 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 description 1
MUBJXSCTPOBLCX-UHFFFAOYSA-N 2-methoxy-1,4-dinitrobenzene Chemical compound COC1=CC([N+]([O-])=O)=CC=C1[N+]([O-])=O MUBJXSCTPOBLCX-UHFFFAOYSA-N 0.000 description 1
GVBUHJSIDPIOBZ-UHFFFAOYSA-N 2-methoxy-3-nitroaniline Chemical compound COC1=C(N)C=CC=C1[N+]([O-])=O GVBUHJSIDPIOBZ-UHFFFAOYSA-N 0.000 description 1
KZBOXYKTSUUBTO-UHFFFAOYSA-N 2-methyl-1,4-dinitrobenzene Chemical compound CC1=CC([N+]([O-])=O)=CC=C1[N+]([O-])=O KZBOXYKTSUUBTO-UHFFFAOYSA-N 0.000 description 1
CFBYEGUGFPZCNF-UHFFFAOYSA-N 2-nitroanisole Chemical compound COC1=CC=CC=C1[N+]([O-])=O CFBYEGUGFPZCNF-UHFFFAOYSA-N 0.000 description 1
ZLCPKMIJYMHZMJ-UHFFFAOYSA-N 2-nitrobenzene-1,3-diol Chemical compound OC1=CC=CC(O)=C1[N+]([O-])=O ZLCPKMIJYMHZMJ-UHFFFAOYSA-N 0.000 description 1
JKIFPWHZEZQCQA-UHFFFAOYSA-N 2-nitrobenzenethiol Chemical compound [O-][N+](=O)C1=CC=CC=C1S JKIFPWHZEZQCQA-UHFFFAOYSA-N 0.000 description 1
UUVUYEVFMFFSMP-UHFFFAOYSA-N 2-nitroethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC[N+]([O-])=O UUVUYEVFMFFSMP-UHFFFAOYSA-N 0.000 description 1
KWMRZXLGCIDAGB-UHFFFAOYSA-N 2-nitroethyl prop-2-enoate Chemical compound [O-][N+](=O)CCOC(=O)C=C KWMRZXLGCIDAGB-UHFFFAOYSA-N 0.000 description 1
VDDQPZYMXOVQDD-UHFFFAOYSA-N 3,3-dinitropropyl prop-2-enoate Chemical compound [O-][N+](=O)C([N+]([O-])=O)CCOC(=O)C=C VDDQPZYMXOVQDD-UHFFFAOYSA-N 0.000 description 1
OXAUFLJQLMOTSU-UHFFFAOYSA-N 3,4-dimethyl-2-nitroaniline Chemical compound CC1=CC=C(N)C([N+]([O-])=O)=C1C OXAUFLJQLMOTSU-UHFFFAOYSA-N 0.000 description 1
LRWWBVBRBWPHBA-UHFFFAOYSA-N 3,4-dimethyl-5-nitroaniline Chemical compound CC1=CC(N)=CC([N+]([O-])=O)=C1C LRWWBVBRBWPHBA-UHFFFAOYSA-N 0.000 description 1
INYDMNPNDHRJQJ-UHFFFAOYSA-N 3,4-dinitrotoluene Chemical compound CC1=CC=C([N+]([O-])=O)C([N+]([O-])=O)=C1 INYDMNPNDHRJQJ-UHFFFAOYSA-N 0.000 description 1
UDQLNMXIULDNCQ-UHFFFAOYSA-N 3,5-dimethyl-2-nitroaniline Chemical compound CC1=CC(C)=C([N+]([O-])=O)C(N)=C1 UDQLNMXIULDNCQ-UHFFFAOYSA-N 0.000 description 1
YXNYMZXPUWOUJT-UHFFFAOYSA-N 3,5-dimethyl-2-nitrophenol Chemical compound CC1=CC(C)=C([N+]([O-])=O)C(O)=C1 YXNYMZXPUWOUJT-UHFFFAOYSA-N 0.000 description 1
VIQHHRZADKSPIM-UHFFFAOYSA-N 3,6-dimethyl-2-nitrophenol Chemical compound CC1=CC=C(C)C([N+]([O-])=O)=C1O VIQHHRZADKSPIM-UHFFFAOYSA-N 0.000 description 1
YYGJRRYSYLLCQH-UHFFFAOYSA-N 3-methyl-2,4,6-trinitrophenol Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1[N+]([O-])=O YYGJRRYSYLLCQH-UHFFFAOYSA-N 0.000 description 1
SOPHXJOERHTMIL-UHFFFAOYSA-N 3-methyl-4,6-dinitro-2-propan-2-ylphenol Chemical compound CC(C)C1=C(C)C([N+]([O-])=O)=CC([N+]([O-])=O)=C1O SOPHXJOERHTMIL-UHFFFAOYSA-N 0.000 description 1
WGYFINWERLNPHR-UHFFFAOYSA-N 3-nitroanisole Chemical compound COC1=CC=CC([N+]([O-])=O)=C1 WGYFINWERLNPHR-UHFFFAOYSA-N 0.000 description 1
KGDIYDUZVHFMHQ-UHFFFAOYSA-N 4,5-dimethyl-2-nitrophenol Chemical compound CC1=CC(O)=C([N+]([O-])=O)C=C1C KGDIYDUZVHFMHQ-UHFFFAOYSA-N 0.000 description 1
PQVHMOLNSYFXIJ-UHFFFAOYSA-N 4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]pyrazole-3-carboxylic acid Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(N1CC2=C(CC1)NN=N2)=O)C(=O)O PQVHMOLNSYFXIJ-UHFFFAOYSA-N 0.000 description 1
GRXZQOTZXAKVLN-UHFFFAOYSA-N 4-methoxy-1,2-dinitrobenzene Chemical compound COC1=CC=C([N+]([O-])=O)C([N+]([O-])=O)=C1 GRXZQOTZXAKVLN-UHFFFAOYSA-N 0.000 description 1
AXBVSRMHOPMXBA-UHFFFAOYSA-N 4-nitrothiophenol Chemical compound [O-][N+](=O)C1=CC=C(S)C=C1 AXBVSRMHOPMXBA-UHFFFAOYSA-N 0.000 description 1
VNXFNSPVHVKLPN-UHFFFAOYSA-N 6-methyl-2,3,4-trinitrophenol Chemical compound CC1=CC([N+]([O-])=O)=C([N+]([O-])=O)C([N+]([O-])=O)=C1O VNXFNSPVHVKLPN-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
AGUIVNYEYSCPNI-UHFFFAOYSA-N N-methyl-N-picrylnitramine Chemical group [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 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
BNUHAJGCKIQFGE-UHFFFAOYSA-N Nitroanisol Chemical compound COC1=CC=C([N+]([O-])=O)C=C1 BNUHAJGCKIQFGE-UHFFFAOYSA-N 0.000 description 1
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 description 1
239000000026 Pentaerythritol tetranitrate Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
UATJOMSPNYCXIX-UHFFFAOYSA-N Trinitrobenzene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 UATJOMSPNYCXIX-UHFFFAOYSA-N 0.000 description 1
YQFGDVOVXBSQKZ-UHFFFAOYSA-N [N+](=O)([O-])C(CC1=CC=CC=C1)([N+](=O)[O-])[N+](=O)[O-].[N+](=O)([O-])C(CC1=CC=CC=C1)[N+](=O)[O-] Chemical compound [N+](=O)([O-])C(CC1=CC=CC=C1)([N+](=O)[O-])[N+](=O)[O-].[N+](=O)([O-])C(CC1=CC=CC=C1)[N+](=O)[O-] YQFGDVOVXBSQKZ-UHFFFAOYSA-N 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
CZZVSJPFJBUBDK-UHFFFAOYSA-N diazonio-(4-nitrophenyl)azanide Chemical compound [O-][N+](=O)C1=CC=C([N-][N+]#N)C=C1 CZZVSJPFJBUBDK-UHFFFAOYSA-N 0.000 description 1
LYAGTVMJGHTIDH-UHFFFAOYSA-N diethylene glycol dinitrate Chemical compound [O-][N+](=O)OCCOCCO[N+]([O-])=O LYAGTVMJGHTIDH-UHFFFAOYSA-N 0.000 description 1
KSHJAFFDLKPUMT-UHFFFAOYSA-N dinitro-ortho-cresol Chemical compound CC1=C(O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O KSHJAFFDLKPUMT-UHFFFAOYSA-N 0.000 description 1
VMMLSJNPNVTYMN-UHFFFAOYSA-N dinitromethylbenzene Chemical class [O-][N+](=O)C([N+]([O-])=O)C1=CC=CC=C1 VMMLSJNPNVTYMN-UHFFFAOYSA-N 0.000 description 1
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000000446 fuel Substances 0.000 description 1
239000001087 glyceryl triacetate Substances 0.000 description 1
235000013773 glyceryl triacetate Nutrition 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000003607 modifier Substances 0.000 description 1
QCOXCILKVHKOGO-UHFFFAOYSA-N n-(2-nitramidoethyl)nitramide Chemical compound [O-][N+](=O)NCCN[N+]([O-])=O QCOXCILKVHKOGO-UHFFFAOYSA-N 0.000 description 1
ARMSTQBMUHJXHU-UHFFFAOYSA-N n-(2-nitrophenyl)benzamide Chemical compound [O-][N+](=O)C1=CC=CC=C1NC(=O)C1=CC=CC=C1 ARMSTQBMUHJXHU-UHFFFAOYSA-N 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
AAAUMZZBNYAFHL-UHFFFAOYSA-N nitro nitroformate Chemical class [O-][N+](=O)OC(=O)[N+]([O-])=O AAAUMZZBNYAFHL-UHFFFAOYSA-N 0.000 description 1
RPMXALUWKZHYOV-UHFFFAOYSA-N nitroethene Chemical group [O-][N+](=O)C=C RPMXALUWKZHYOV-UHFFFAOYSA-N 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
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 1
229960004321 pentaerithrityl tetranitrate Drugs 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920001004 polyvinyl nitrate Polymers 0.000 description 1
159000000001 potassium salts Chemical class 0.000 description 1
OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
229910052939 potassium sulfate Inorganic materials 0.000 description 1
239000001120 potassium sulphate Substances 0.000 description 1
235000011151 potassium sulphates Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000012254 powdered material Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L sodium sulphate Substances [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229960002622 triacetin Drugs 0.000 description 1
AGCQZYRSTIRJFM-UHFFFAOYSA-N triethylene glycol dinitrate Chemical compound [O-][N+](=O)OCCOCCOCCO[N+]([O-])=O AGCQZYRSTIRJFM-UHFFFAOYSA-N 0.000 description 1
IPPYBNCEPZCLNI-UHFFFAOYSA-N trimethylolethane trinitrate Chemical compound [O-][N+](=O)OCC(C)(CO[N+]([O-])=O)CO[N+]([O-])=O IPPYBNCEPZCLNI-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/04—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
- C06B45/06—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component
- C06B45/10—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component the organic component containing a resin
- C06B45/105—The resin being a polymer bearing energetic groups or containing a soluble organic explosive
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B25/00—Compositions containing a nitrated organic compound
- C06B25/34—Compositions containing a nitrated organic compound the compound being a nitrated acyclic, alicyclic or heterocyclic amine

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Dispersion Chemistry (AREA)
Molecular Biology (AREA)
Crystallography & Structural Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

SE8801944A 1986-07-04 1988-05-25 Energetiska material SE500687C2 (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB868616322A GB8616322D0 (en)	1985-07-08	1986-07-04	Conduit fitting

Publications (3)

Publication Number	Publication Date
SE8801944D0 SE8801944D0 (sv)	1988-05-25
SE8801944L SE8801944L (sv)	1991-09-06
SE500687C2 true SE500687C2 (sv)	1994-08-08

Family

ID=10600560

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8801944A SE500687C2 (sv)	1986-07-04	1988-05-25	Energetiska material

Country Status (9)

Country	Link
AU (1)	AU663677B1 (fr)
BE (1)	BE1005565A7 (fr)
CA (1)	CA1325518C (fr)
DE (1)	DE3744680C2 (fr)
FR (1)	FR2664587B1 (fr)
GB (1)	GB2243826B (fr)
IT (1)	IT1235712B (fr)
NL (1)	NL194964C (fr)
SE (1)	SE500687C2 (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5540794A (en) *	1992-05-11	1996-07-30	Thiokol Corporation	Energetic binder and thermoplastic elastomer-based low vulnerability ammunition gun propellants with improved mechanical properties
SE470480B (sv) *	1992-10-02	1994-05-24	Bofors Explosives Ab	Drivmedel för Air bags
US5487851A (en) *	1993-12-20	1996-01-30	Thiokol Corporation	Composite gun propellant processing technique
US6214137B1 (en) *	1997-10-07	2001-04-10	Cordant Technologies Inc.	High performance explosive containing CL-20
EP1044180B1 (fr) *	1998-01-05	2018-04-11	Dynamit Nobel Defence GmbH	Utilisation de composés nitrés
US6241833B1 (en) *	1998-07-16	2001-06-05	Alliant Techsystems, Inc.	High energy gun propellants
WO2001046091A1 (fr) *	1999-12-22	2001-06-28	Doll, Daniel, W.	Explosifs moules par fusion a sensibilite reduite
US6964714B2 (en)	2001-06-27	2005-11-15	Alliant Techsystems Inc.	Reduced sensitivity, melt-pourable tritonal replacements
US7067024B2 (en)	2001-06-27	2006-06-27	Alliant Techsystems Inc.	Reduced sensitivity, melt-pourable TNT replacements
DE102010020776B4 (de) *	2010-05-18	2015-03-05	Diehl Bgt Defence Gmbh & Co. Kg	Treibladung und Verfahren zu ihrer Herstellung

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3528864A (en) *	1965-09-21	1970-09-15	Us Navy	High impulse explosives containing tungsten
DE2329558C3 (de) *	1973-06-09	1978-10-05	Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung E.V., 8000 Muenchen	Gießfähige Gasgeneratortreibstoffe
DE2365595A1 (de) *	1973-07-14	1975-10-02	Messerschmitt Boelkow Blohm	Hochleistungssprengkoerper
DE2336004A1 (de) *	1973-07-14	1975-02-13	Messerschmitt Boelkow Blohm	Hochleistungs-sprengstoff-formkoerper und verfahren zu ihrer herstellung
DE2709949C2 (de) *	1977-03-08	1982-09-16	Messerschmitt-Bölkow-Blohm GmbH, 8000 München	Kristalliner Hochleistungssprengstoff
US4092188A (en) *	1977-05-16	1978-05-30	Lovelace Alan M Acting Adminis	Nitramine propellants
DE2753555C1 (de) *	1977-12-01	1990-09-20	Dynamit Nobel Ag	Verwendung von polymeren Polynitroaromaten in Treibsaetzen
DE3023462A1 (de) *	1980-06-24	1984-02-23	Dynamit Nobel Ag, 5210 Troisdorf	Nitrierte arylaether

1987
- 1987-07-02 BE BE0000114A patent/BE1005565A7/fr active
- 1987-07-02 DE DE3744680A patent/DE3744680C2/de not_active Expired - Lifetime
- 1987-07-02 NL NL8715010A patent/NL194964C/nl not_active IP Right Cessation
- 1987-07-03 CA CA000541310A patent/CA1325518C/fr not_active Expired - Fee Related
- 1987-07-06 AU AU75645/87A patent/AU663677B1/en not_active Ceased
- 1987-07-06 GB GB8715870A patent/GB2243826B/en not_active Expired - Lifetime
1988
- 1988-02-23 FR FR8802281A patent/FR2664587B1/fr not_active Expired - Fee Related
- 1988-04-18 IT IT8847864A patent/IT1235712B/it active
- 1988-05-25 SE SE8801944A patent/SE500687C2/sv not_active IP Right Cessation

Also Published As

Publication number	Publication date
SE8801944D0 (sv)	1988-05-25
IT1235712B (it)	1992-09-24
DE3744680C2 (de)	1996-10-02
IT8847864A0 (it)	1988-04-18
FR2664587A1 (fr)	1992-01-17
NL194964B (nl)	2003-05-01
NL8715010A (nl)	1991-10-01
SE8801944L (sv)	1991-09-06
GB2243826A (en)	1991-11-13
DE3744680A1 (de)	1991-11-28
FR2664587B1 (fr)	1993-09-24
GB8715870D0 (en)	1991-06-12
AU663677B1 (en)	1995-10-19
NL194964C (nl)	2003-09-02
GB2243826B (en)	1992-03-25
BE1005565A7 (fr)	1993-06-15
CA1325518C (fr)	1993-12-28

Legal Events

Date	Code	Title	Description
2006-03-21	NUG	Patent has lapsed

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