SE513930C2 - Flytande drivmedel - Google Patents
Flytande drivmedelInfo
- Publication number
- SE513930C2 SE513930C2 SE9900715A SE9900715A SE513930C2 SE 513930 C2 SE513930 C2 SE 513930C2 SE 9900715 A SE9900715 A SE 9900715A SE 9900715 A SE9900715 A SE 9900715A SE 513930 C2 SE513930 C2 SE 513930C2
- Authority
- SE
- Sweden
- Prior art keywords
- fuel
- solvent
- water
- weight
- glycerol
- Prior art date
Links
- 239000000446 fuel Substances 0.000 title claims abstract description 92
- 239000007788 liquid Substances 0.000 title claims abstract description 8
- 239000003380 propellant Substances 0.000 claims abstract description 27
- -1 dinitramide compound Chemical class 0.000 claims abstract description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 60
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 33
- 239000000203 mixture Substances 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 20
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 10
- 229920006395 saturated elastomer Polymers 0.000 claims description 10
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 8
- 150000002576 ketones Chemical class 0.000 claims description 7
- 150000001768 cations Chemical group 0.000 claims description 6
- 239000004471 Glycine Substances 0.000 claims description 4
- 150000001299 aldehydes Chemical class 0.000 claims description 4
- 150000001413 amino acids Chemical class 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000012047 saturated solution Substances 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 claims description 2
- 229910001410 inorganic ion Inorganic materials 0.000 claims description 2
- 150000003141 primary amines Chemical class 0.000 claims description 2
- 150000005846 sugar alcohols Polymers 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract description 33
- 231100000331 toxic Toxicity 0.000 abstract description 5
- 230000002588 toxic effect Effects 0.000 abstract description 5
- 231100000053 low toxicity Toxicity 0.000 abstract description 3
- 230000035945 sensitivity Effects 0.000 abstract description 3
- 239000007789 gas Substances 0.000 abstract description 2
- BRUFJXUJQKYQHA-UHFFFAOYSA-O ammonium dinitramide Chemical compound [NH4+].[O-][N+](=O)[N-][N+]([O-])=O BRUFJXUJQKYQHA-UHFFFAOYSA-O 0.000 description 21
- 239000007800 oxidant agent Substances 0.000 description 19
- 235000011187 glycerol Nutrition 0.000 description 18
- 238000004364 calculation method Methods 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000002485 combustion reaction Methods 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 238000007248 oxidative elimination reaction Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- MJVUDZGNBKFOBF-UHFFFAOYSA-N n-nitronitramide Chemical compound [O-][N+](=O)N[N+]([O-])=O MJVUDZGNBKFOBF-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000011973 solid acid Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- UOQFZGVGGMHGEE-UHFFFAOYSA-N 1,1-dihydroxypropan-2-one Chemical compound CC(=O)C(O)O UOQFZGVGGMHGEE-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical class CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- AJPXOOXHHFMBQS-UHFFFAOYSA-N N[N+]([O-])=O.N[N+]([O-])=O.NO Chemical compound N[N+]([O-])=O.N[N+]([O-])=O.NO AJPXOOXHHFMBQS-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 group 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- ZSCWLAADLCMTDR-UHFFFAOYSA-N azane;ethanol;methanol;propan-2-one Chemical compound N.OC.CCO.CC(C)=O ZSCWLAADLCMTDR-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001739 density measurement Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- YMBNBZFZTXCWDV-UHFFFAOYSA-N ethane-1,2-diol;propane-1,2,3-triol Chemical compound OCCO.OCC(O)CO YMBNBZFZTXCWDV-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 229910001416 lithium ion Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N methyl monoether Natural products COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- VDUIPQNXOQMTBF-UHFFFAOYSA-N n-ethylhydroxylamine Chemical compound CCNO VDUIPQNXOQMTBF-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- FVGBHSIHHXTYTH-UHFFFAOYSA-N pentane-1,1,1-triol Chemical compound CCCCC(O)(O)O FVGBHSIHHXTYTH-UHFFFAOYSA-N 0.000 description 1
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000004449 solid propellant Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B47/00—Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B31/00—Compositions containing an inorganic nitrogen-oxygen salt
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D5/00—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
- C06D5/08—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets by reaction of two or more liquids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Filling Or Discharging Of Gas Storage Vessels (AREA)
- Feeding, Discharge, Calcimining, Fusing, And Gas-Generation Devices (AREA)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/258,390 US6254705B1 (en) | 1999-02-26 | 1999-02-26 | Liquid propellant |
| SE9900715A SE513930C2 (sv) | 1999-02-26 | 1999-02-26 | Flytande drivmedel |
| AU34680/00A AU3468000A (en) | 1999-02-26 | 2000-02-23 | Dinitramide based liquid mono-propellants |
| IL14474300A IL144743A (en) | 1999-02-26 | 2000-02-23 | Dinitramide based liquid mono-propellants |
| EP00913204A EP1192115B1 (de) | 1999-02-26 | 2000-02-23 | Dinitramid enthaltende treibstoffzusammensetzung |
| BR0008548-0A BR0008548A (pt) | 1999-02-26 | 2000-02-23 | Formulação de mono-propelente lìquido |
| DE60003429T DE60003429T2 (de) | 1999-02-26 | 2000-02-23 | Dinitramid enthaltende treibstoffzusammensetzung |
| RU2001126122/02A RU2244704C2 (ru) | 1999-02-26 | 2000-02-23 | Жидкое одноосновное ракетное топливо на основе динитрамида |
| PCT/SE2000/000358 WO2000050363A1 (en) | 1999-02-26 | 2000-02-23 | Dinitramide based liquid mono-propellants |
| CNB008042454A CN1321950C (zh) | 1999-02-26 | 2000-02-23 | 二硝酰胺基液体单组份推进剂 |
| AT00913204T ATE243177T1 (de) | 1999-02-26 | 2000-02-23 | Dinitramid enthaltende treibstoffzusammensetzung |
| JP2000600948A JP4536262B2 (ja) | 1999-02-26 | 2000-02-23 | ジニトラミド系液体モノ推進剤 |
| NO20014152A NO20014152L (no) | 1999-02-26 | 2001-08-27 | Dinitramidbaserte flytende mono-drivmidler |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9900715A SE513930C2 (sv) | 1999-02-26 | 1999-02-26 | Flytande drivmedel |
| US09/258,390 US6254705B1 (en) | 1999-02-26 | 1999-02-26 | Liquid propellant |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE9900715D0 SE9900715D0 (sv) | 1999-02-26 |
| SE9900715L SE9900715L (sv) | 2000-08-27 |
| SE513930C2 true SE513930C2 (sv) | 2000-11-27 |
Family
ID=26663519
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE9900715A SE513930C2 (sv) | 1999-02-26 | 1999-02-26 | Flytande drivmedel |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6254705B1 (de) |
| EP (1) | EP1192115B1 (de) |
| JP (1) | JP4536262B2 (de) |
| CN (1) | CN1321950C (de) |
| AT (1) | ATE243177T1 (de) |
| AU (1) | AU3468000A (de) |
| BR (1) | BR0008548A (de) |
| DE (1) | DE60003429T2 (de) |
| IL (1) | IL144743A (de) |
| NO (1) | NO20014152L (de) |
| RU (1) | RU2244704C2 (de) |
| SE (1) | SE513930C2 (de) |
| WO (1) | WO2000050363A1 (de) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014084344A1 (ja) * | 2012-11-30 | 2014-06-05 | カーリットホールディングス株式会社 | 液体推進薬 |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0950648A1 (de) * | 1998-04-15 | 1999-10-20 | Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno | Monergoles flüssiges Treibstoffsystem |
| SE0101751D0 (sv) * | 2001-05-28 | 2001-05-28 | Svenska Rymdaktiebolaget | Ammonium dinitramide based liquid monopropellants exhibiting improved cumbustion stability and storage life |
| US7083690B2 (en) | 2001-07-03 | 2006-08-01 | Wiley Organics, Inc. | Catalyst system for rendering organic propellants hypergolic with hydrogen peroxide |
| DE60221679D1 (de) * | 2001-08-27 | 2007-09-20 | Wiley Organics Inc | Alkynylsilane als brennstoff und treibstoffe für raketen |
| US8894782B2 (en) | 2002-09-03 | 2014-11-25 | Wiley Organics, Inc. | Hypergolic hydrocarbon fuels |
| JP4500576B2 (ja) * | 2004-04-01 | 2010-07-14 | ダイセル化学工業株式会社 | ガス発生剤組成物 |
| JP4500586B2 (ja) * | 2004-05-31 | 2010-07-14 | ダイセル化学工業株式会社 | ガス発生剤組成物 |
| US8034133B2 (en) | 2004-05-31 | 2011-10-11 | Daicel Chemical Industries, Ltd. | Gas generating composition |
| US7598002B2 (en) * | 2005-01-11 | 2009-10-06 | Material Methods Llc | Enhanced electrochemical cells with solid-electrolyte interphase promoters |
| WO2006126397A1 (ja) * | 2005-05-26 | 2006-11-30 | National University Corporation Kyushu Institute Of Technology | 二液式液体推進薬、飛行体推進方法および推進機 |
| US7966805B2 (en) * | 2007-05-15 | 2011-06-28 | Raytheon Company | Hydroxyl amine based staged combustion hybrid rocket motor |
| JP5711536B2 (ja) * | 2007-11-09 | 2015-05-07 | ファイアースター エンジニアリング，エルエルシー | 一酸化二窒素と燃料とが混合されて成るモノプロペラント |
| US9481840B2 (en) * | 2009-04-13 | 2016-11-01 | University Of Alabama In Huntsville | Hydroxyethylhydrazinium nitrate-acetone formulations and methods of making hydroxyethylhydrazinium nitrate-acetone formulations |
| WO2012166046A2 (en) * | 2011-06-01 | 2012-12-06 | Ecaps Ab | Low-temperature operational and storable ammonium dinitramide based liquid monopropellant blends |
| CN102320906B (zh) * | 2011-08-16 | 2013-03-06 | 湖北三江航天江河化工科技有限公司 | 一种酰胺类助剂及其制备方法 |
| WO2013048315A2 (en) | 2011-09-26 | 2013-04-04 | Ecaps Aktiebolag | Method and arrangement for conversion of chemical energy from aqueous, liquid, adn-based monopropellants into mechanical energy |
| FR2986229B1 (fr) | 2012-01-27 | 2014-03-21 | Centre Nat Detudes Spatiales Cnes | Nouveaux monergols ioniques a base de n2o pour la propulsion spatiale |
| EP2847452B1 (de) * | 2012-05-09 | 2016-11-30 | ECAPS Aktiebolag | Verbesserter reaktor für auf ammoniumdinitramid basierende flüssige monotreibmittel und triebwerk mit dem reaktor |
| RU2547476C2 (ru) * | 2012-07-04 | 2015-04-10 | Николай Евгеньевич Староверов | Ракетное топливо (варианты) |
| RU2523367C2 (ru) * | 2012-07-09 | 2014-07-20 | Николай Евгеньевич Староверов | Ракетное горючее |
| RU2516825C1 (ru) * | 2012-10-08 | 2014-05-20 | Николай Евгеньевич Староверов | Ракетное топливо староверова - 14 (варианты) |
| RU2516711C1 (ru) * | 2012-10-16 | 2014-05-20 | Николай Евгеньевич Староверов | Ракетное топливо староверова - 15 (варианты) |
| US9182207B2 (en) * | 2012-10-24 | 2015-11-10 | Digital Solid State Propulsion, Inc. | Liquid electrically initiated and controlled gas generator composition |
| CN103159577B (zh) * | 2013-03-27 | 2015-09-02 | 北京理工大学 | 一种含adn的水下高能炸药及其制备方法 |
| WO2014189450A1 (en) * | 2013-05-20 | 2014-11-27 | Ecaps Ab | Oxidizer-rich liquid monopropellants for a dual mode chemical rocket engine |
| WO2014193300A1 (en) | 2013-05-29 | 2014-12-04 | Ecaps Ab | Dual mode chemical rocket engine, and dual mode propulsion system comprising the rocket engine |
| RU2570012C1 (ru) * | 2014-05-13 | 2015-12-10 | Николай Евгеньевич Староверов | Ракетное топливо староверова - 3 /варианты/ |
| JP2015218096A (ja) * | 2014-05-20 | 2015-12-07 | カーリットホールディングス株式会社 | 液体推進薬 |
| RU2572886C1 (ru) * | 2014-06-17 | 2016-01-20 | Николай Евгеньевич Староверов | Ракетное топливо староверова - 17 /варианты/ |
| RU2570444C1 (ru) * | 2014-06-17 | 2015-12-10 | Николай Евгеньевич Староверов | Ракетное топливо староверова - 19 /варианты/ |
| RU2572887C1 (ru) * | 2014-07-04 | 2016-01-20 | Николай Евгеньевич Староверов | Ракетное топливо староверова - 20 /варианты/ |
| JP6472628B2 (ja) * | 2014-09-30 | 2019-02-20 | カーリットホールディングス株式会社 | 液体推進薬の製造方法 |
| DE102014016299A1 (de) * | 2014-11-06 | 2016-05-12 | Deutsches Zentrum für Luft- und Raumfahrt e.V. (DLR) | Gasgenerator-Treibstoff auf der Basis von Ammoniumdinitramid (ADN) und Verfahren zu seiner Herstellung |
| JP7088740B2 (ja) * | 2018-05-17 | 2022-06-21 | カーリットホールディングス株式会社 | 液体推進剤およびその添加剤 |
| JP7250304B2 (ja) * | 2018-09-26 | 2023-04-03 | 国立大学法人室蘭工業大学 | タービン駆動用ガスジェネレータの推進剤及びその製造方法 |
| CN109694044B (zh) * | 2018-12-21 | 2020-09-18 | 湖北航天化学技术研究所 | 一种二硝酰胺羟胺的制备方法 |
| WO2023026312A1 (ja) * | 2021-08-22 | 2023-03-02 | 合同会社パッチドコニックス | 宇宙機搭載の推進剤および推進機関と、それらの方法 |
| CN116217314B (zh) * | 2023-04-25 | 2024-01-23 | 湖北航天化学技术研究所 | 一种复合含能粒子及其制备方法 |
| CN118908794B (zh) * | 2024-10-12 | 2024-12-27 | 中国科学院大连化学物理研究所 | 一种低碳富氮二硝酰胺铵液体推进剂及其制备方法和应用 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5223057A (en) | 1969-03-28 | 1993-06-29 | The United States Of America As Represented By The Secretary Of The Navy | Monopropellant aqueous hydroxyl ammonium nitrate/fuel |
| US5256220A (en) * | 1979-12-03 | 1993-10-26 | The United States Of America As Represented By The Secretary Of The Navy | Liquid monopropellants |
| US5254324A (en) * | 1990-06-18 | 1993-10-19 | Sri International | Dinitramide salts and method of making same |
| US5714714A (en) * | 1992-10-15 | 1998-02-03 | The United States Of America As Represented By The Secretary Of The Navy | Process for preparing ammonium dinitramide |
| US5292387A (en) * | 1993-01-28 | 1994-03-08 | Thiokol Corporation | Phase-stabilized ammonium nitrate and method of making same |
| US5324075A (en) * | 1993-02-02 | 1994-06-28 | Trw Inc. | Gas generator for vehicle occupant restraint |
| US5529649A (en) * | 1993-02-03 | 1996-06-25 | Thiokol Corporation | Insensitive high performance explosive compositions |
| US5498303A (en) | 1993-04-21 | 1996-03-12 | Thiokol Corporation | Propellant formulations based on dinitramide salts and energetic binders |
| US5441720A (en) * | 1993-07-13 | 1995-08-15 | The United States Of America As Represented By The Secretary Of The Navy | Pentafluorosulfanylnitramide salts |
| US5467714A (en) * | 1993-12-16 | 1995-11-21 | Thiokol Corporation | Enhanced performance, high reaction temperature explosive |
| US5587553A (en) * | 1994-11-07 | 1996-12-24 | Thiokol Corporation | High performance pressable explosive compositions |
| US5468313A (en) * | 1994-11-29 | 1995-11-21 | Thiokol Corporation | Plastisol explosive |
| US5868424A (en) * | 1996-03-06 | 1999-02-09 | Oea, Inc. | Substantially smoke-free and particulate-free inflator for inflatable safety restraint system |
| US5684269A (en) * | 1996-03-15 | 1997-11-04 | Morton International, Inc. | Hydroxylammonium nitrate/water/self-deflagrating fuels as gas generating pyrotechnics for use in automotive passive restraint systems |
| US6120058A (en) | 1996-08-23 | 2000-09-19 | Trw Vehicle Safety Systems Inc. | Air bag inflator |
| US5780769A (en) * | 1996-08-26 | 1998-07-14 | The United States Of America As Represented By The Secretary Of The Navy | Thermal stabilization of N,N-dinitramide salts |
| US5962808A (en) * | 1997-03-05 | 1999-10-05 | Automotive Systems Laboratory, Inc. | Gas generant complex oxidizers |
| JP3884127B2 (ja) * | 1997-06-30 | 2007-02-21 | 細谷火工株式会社 | 一液推進方法および一液推進装置 |
| EP0950648A1 (de) * | 1998-04-15 | 1999-10-20 | Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno | Monergoles flüssiges Treibstoffsystem |
| US5889161A (en) * | 1998-05-13 | 1999-03-30 | Sri International | N,N'-azobis-nitroazoles and analogs thereof as igniter compounds for use in energetic compositions |
-
1999
- 1999-02-26 SE SE9900715A patent/SE513930C2/sv not_active IP Right Cessation
- 1999-02-26 US US09/258,390 patent/US6254705B1/en not_active Expired - Lifetime
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2000
- 2000-02-23 AT AT00913204T patent/ATE243177T1/de not_active IP Right Cessation
- 2000-02-23 JP JP2000600948A patent/JP4536262B2/ja not_active Expired - Fee Related
- 2000-02-23 RU RU2001126122/02A patent/RU2244704C2/ru not_active IP Right Cessation
- 2000-02-23 IL IL14474300A patent/IL144743A/en not_active IP Right Cessation
- 2000-02-23 EP EP00913204A patent/EP1192115B1/de not_active Expired - Lifetime
- 2000-02-23 AU AU34680/00A patent/AU3468000A/en not_active Abandoned
- 2000-02-23 DE DE60003429T patent/DE60003429T2/de not_active Expired - Lifetime
- 2000-02-23 BR BR0008548-0A patent/BR0008548A/pt not_active Application Discontinuation
- 2000-02-23 WO PCT/SE2000/000358 patent/WO2000050363A1/en not_active Ceased
- 2000-02-23 CN CNB008042454A patent/CN1321950C/zh not_active Expired - Fee Related
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014084344A1 (ja) * | 2012-11-30 | 2014-06-05 | カーリットホールディングス株式会社 | 液体推進薬 |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2244704C2 (ru) | 2005-01-20 |
| NO20014152D0 (no) | 2001-08-27 |
| DE60003429D1 (de) | 2003-07-24 |
| ATE243177T1 (de) | 2003-07-15 |
| JP4536262B2 (ja) | 2010-09-01 |
| IL144743A (en) | 2004-06-20 |
| WO2000050363A1 (en) | 2000-08-31 |
| EP1192115B1 (de) | 2003-06-18 |
| IL144743A0 (en) | 2002-06-30 |
| SE9900715L (sv) | 2000-08-27 |
| AU3468000A (en) | 2000-09-14 |
| SE9900715D0 (sv) | 1999-02-26 |
| EP1192115A1 (de) | 2002-04-03 |
| US6254705B1 (en) | 2001-07-03 |
| DE60003429T2 (de) | 2004-05-06 |
| JP2002537218A (ja) | 2002-11-05 |
| CN1321950C (zh) | 2007-06-20 |
| BR0008548A (pt) | 2001-11-06 |
| CN1341086A (zh) | 2002-03-20 |
| NO20014152L (no) | 2001-09-27 |
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