NL194964C - Energierijke samenstelling. - Google Patents

Energierijke samenstelling. Download PDF

Info

Publication number: NL194964C
Authority: NL; Netherlands
Prior art keywords: component; weight; composition according; composition; energy
Prior art date: 1986-07-04

Application number

NL8715010A

Other languages

English (en)

Dutch (nl)

Other versions

NL194964B (nl

NL8715010A (nl

Original Assignee

Bae Systems 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

1987-07-02

Publication date

2003-09-02

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

1987-07-02 Application filed by Bae Systems Plc filed Critical Bae Systems Plc

1991-10-01 Publication of NL8715010A publication Critical patent/NL8715010A/nl

2003-05-01 Publication of NL194964B publication Critical patent/NL194964B/nl

2003-09-02 Application granted granted Critical

2003-09-02 Publication of NL194964C publication Critical patent/NL194964C/nl

Links

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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
BBUPBICWUURTNP-UHFFFAOYSA-N 2,4-dimethyl-1-nitrobenzene Chemical compound CC1=CC=C([N+]([O-])=O)C(C)=C1 BBUPBICWUURTNP-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
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
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
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
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
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Natural products CC=O IKHGUXGNUITLKF-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-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 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
229910002651 NO3 Inorganic materials 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
239000000026 Pentaerythritol tetranitrate Substances 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 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
GTTSNKDQDACYLV-UHFFFAOYSA-N Trihydroxybutane Chemical compound CCCC(O)(O)O GTTSNKDQDACYLV-UHFFFAOYSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920001577 copolymer Polymers 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
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
229960001826 dimethylphthalate Drugs 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
238000001035 drying Methods 0.000 description 1
230000003628 erosive effect Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000001087 glyceryl triacetate Substances 0.000 description 1
235000013773 glyceryl triacetate Nutrition 0.000 description 1
238000000227 grinding Methods 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
238000010348 incorporation Methods 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
AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
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 description 1
239000003607 modifier Substances 0.000 description 1
125000002950 monocyclic group Chemical group 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
150000002823 nitrates Chemical class 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
RPMXALUWKZHYOV-UHFFFAOYSA-N nitroethene Chemical group [O-][N+](=O)C=C RPMXALUWKZHYOV-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group 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
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920001004 polyvinyl nitrate Polymers 0.000 description 1
229940086066 potassium hydrogencarbonate Drugs 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
235000011151 potassium sulphates Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000012254 powdered material Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000003825 pressing Methods 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
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
235000021286 stilbenes Nutrition 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
150000005186 trinitrobenzenes Chemical class 0.000 description 1
229920006305 unsaturated polyester Polymers 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)

NL8715010A 1986-07-04 1987-07-02 Energierijke samenstelling. NL194964C (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB868616322A GB8616322D0 (en)	1985-07-08	1986-07-04	Conduit fitting
GB8616322		1986-07-04

Publications (3)

Publication Number	Publication Date
NL8715010A NL8715010A (nl)	1991-10-01
NL194964B NL194964B (nl)	2003-05-01
NL194964C true NL194964C (nl)	2003-09-02

Family

ID=10600560

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8715010A NL194964C (nl)	1986-07-04	1987-07-02	Energierijke samenstelling.

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
GB2243826B (en)	1992-03-25
BE1005565A7 (fr)	1993-06-15
CA1325518C (fr)	1993-12-28
SE500687C2 (sv)	1994-08-08

Legal Events

Date	Code	Title	Description
1994-06-01	BA	A request for search or an international-type search has been filed
1994-11-01	BB	A search report has been drawn up
1995-02-01	BC	A request for examination has been filed
2003-10-01	CNR	Transfer of rights (patent application after its laying open for public inspection)	Owner name: BAE SYSTEMS PLC
2006-04-03	V1	Lapsed because of non-payment of the annual fee	Effective date: 20060201

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