EP2448885A1 - Verfahren zur herstellung von festen zusammengesetzten aluminisierten treibstoffen und feste zusammengesetzte aluminisierte treibstoffe - Google Patents
Verfahren zur herstellung von festen zusammengesetzten aluminisierten treibstoffen und feste zusammengesetzte aluminisierte treibstoffeInfo
- Publication number
- EP2448885A1 EP2448885A1 EP10745374A EP10745374A EP2448885A1 EP 2448885 A1 EP2448885 A1 EP 2448885A1 EP 10745374 A EP10745374 A EP 10745374A EP 10745374 A EP10745374 A EP 10745374A EP 2448885 A1 EP2448885 A1 EP 2448885A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- charge
- ammonium perchlorate
- weight
- value
- particle size
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 25
- 239000003380 propellant Substances 0.000 title abstract description 75
- 239000007787 solid Substances 0.000 title abstract description 8
- 238000004519 manufacturing process Methods 0.000 title abstract description 7
- 239000002245 particle Substances 0.000 claims abstract description 102
- 239000004449 solid propellant Substances 0.000 claims abstract description 58
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 claims abstract description 40
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 35
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 35
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 32
- 238000009826 distribution Methods 0.000 claims abstract description 20
- 239000011230 binding agent Substances 0.000 claims abstract description 8
- 239000004814 polyurethane Substances 0.000 claims abstract description 6
- 229920002635 polyurethane Polymers 0.000 claims abstract description 6
- 238000002485 combustion reaction Methods 0.000 claims description 58
- 239000000203 mixture Substances 0.000 claims description 33
- 230000001590 oxidative effect Effects 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 25
- 239000007788 liquid Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- 229920005862 polyol Polymers 0.000 claims description 8
- 150000003077 polyols Chemical class 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 6
- 239000004014 plasticizer Substances 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 5
- 239000003431 cross linking reagent Substances 0.000 claims description 5
- 238000004132 cross linking Methods 0.000 claims description 4
- 238000005266 casting Methods 0.000 claims description 3
- 230000010355 oscillation Effects 0.000 abstract description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 238000001033 granulometry Methods 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000000149 argon plasma sintering Methods 0.000 description 4
- 230000001186 cumulative effect Effects 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 239000000470 constituent Substances 0.000 description 3
- 230000001955 cumulated effect Effects 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 3
- DMYOHQBLOZMDLP-UHFFFAOYSA-N 1-[2-(2-hydroxy-3-piperidin-1-ylpropoxy)phenyl]-3-phenylpropan-1-one Chemical compound C1CCCCN1CC(O)COC1=CC=CC=C1C(=O)CCC1=CC=CC=C1 DMYOHQBLOZMDLP-UHFFFAOYSA-N 0.000 description 2
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 229920001079 Thiokol (polymer) Polymers 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- GKGXKPRVOZNVPQ-UHFFFAOYSA-N diisocyanatomethylcyclohexane Chemical compound O=C=NC(N=C=O)C1CCCCC1 GKGXKPRVOZNVPQ-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 239000003517 fume Substances 0.000 description 2
- 238000013178 mathematical model Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- GBLPOPTXAXWWPO-UHFFFAOYSA-N 8-methylnonyl nonanoate Chemical compound CCCCCCCCC(=O)OCCCCCCCC(C)C GBLPOPTXAXWWPO-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000002902 bimodal effect Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- ZKXWKVVCCTZOLD-UHFFFAOYSA-N copper;4-hydroxypent-3-en-2-one Chemical compound [Cu].CC(O)=CC(C)=O.CC(O)=CC(C)=O ZKXWKVVCCTZOLD-UHFFFAOYSA-N 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011981 development test Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- WDMPYXXSNYABKC-UHFFFAOYSA-N diazanium diperchlorate Chemical compound [NH4+].[NH4+].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O WDMPYXXSNYABKC-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- NHWGPUVJQFTOQX-UHFFFAOYSA-N ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium Chemical compound CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC NHWGPUVJQFTOQX-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- -1 isooctyl Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- QMMIOCOGDRYCEN-UHFFFAOYSA-N n-bis(2-methylaziridin-1-yl)phosphorylmethanamine Chemical compound C1C(C)N1P(=O)(NC)N1CC1C QMMIOCOGDRYCEN-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000001141 propulsive effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000002604 ultrasonography 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
- C06B33/00—Compositions containing particulate metal, alloy, boron, silicon, selenium or tellurium with at least one oxygen supplying material which is either a metal oxide or a salt, organic or inorganic, capable of yielding a metal oxide
- C06B33/06—Compositions containing particulate metal, alloy, boron, silicon, selenium or tellurium with at least one oxygen supplying material which is either a metal oxide or a salt, organic or inorganic, capable of yielding a metal oxide the material being an inorganic oxygen-halogen salt
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B29/00—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate
- C06B29/02—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate of an alkali metal
- C06B29/16—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate of an alkali metal with a nitrated organic compound
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B29/00—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate
- C06B29/22—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate the salt being ammonium perchlorate
-
- 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
- C06B45/02—Compositions or products which are defined by structure or arrangement of component of product comprising particles of diverse size or shape
-
- 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
Definitions
- the main objects of the present invention are:
- a process for obtaining a composite solid propellant (with a polyurethane binder loaded with ammonium perchlorate and aluminum), such a solid composite propellant, solid propellant charges and the associated rocket engines.
- the invention is in the field of solid propellant propulsion and more particularly relates to aluminized composite solid propellants.
- the object of the invention is to reduce the alumina deposits at the bottom of the engines with integrated nozzle and tend to reduce aerodynamic thrust oscillations while maintaining the ballistic properties, including the combustion rates, the propellants similar to industrial propellants for space application known to date.
- the solid propellant engines for space launchers are of the type of the Ariane 5 rocket or the American Space Shuttle, large (h ⁇ 20 m, D ⁇ 5 m), with integrated nozzle.
- the solid propellant loads contained in this type of engine have a mass ranging from a few hundred kilograms to several hundred tons. Their operating time is of the order of a few tens of seconds to a few minutes.
- the present invention is in this context large solid propellant engines.
- Solid propellants for these applications are composite propellants with an inert binder of the polyurethane type. They contain a charge of ammonium perchlorate (oxidizing charge) and an aluminum charge (reducing charge).
- the oxidizing charge of ammonium perchlorate contained in said propellants generally consists of the several charges of perchlorate of ammonium of different monomodal particle size distributions which have been added in the preparation of said propellants. It may be the same for the reducing load of aluminum.
- This family of propellants is that concerned by the present invention.
- the mass ratios of these ingredients are generally about 68% for ammonium perchlorate, 20% for aluminum and 12% for binder.
- the burning rate of the solid propellant depends on the pressure P prevailing in the combustion chamber and conventionally follows a law (called the law of old) expressed in the form:
- Vc aP n .
- Said combustion rate Vc and the pressure exponent n of the propellant are fundamental parameters for the ballistic adjustment of a solid propellant engine (combustion time, thrust, combustion stability, etc.),
- the aluminized composite propellants produce, during their combustion, gases and solid particles consisting mainly of alumina (about 30% of the mass ejected by the propellant).
- the aluminum introduced into the aluminized composite solid propellants is in the form of grains, more or less spherical, with a median diameter generally between 1 and 50 microns.
- the combustion of a drop of aluminum, expelled from the burning surface is shown schematically in Figure 1 attached. A flame surrounds the drop of aluminum and a cap of alumina is formed at the bottom of the drop. The combustion generates fumes of alumina (drops of small size, of the order of 1 ⁇ m) and larger drops of alumina from the cap, which explains the bimodal particle size distributions of alumina finally produced by solid propellants.
- the alumina generated by the combustion of the aluminized propellant represents, as indicated above, approximately 30% of the mass ejected by the propellant.
- This non-expelled mass penalizes, on the one hand, the performance of the engine and can, on the other hand, generate, after the extinction of the engine and by a vacuum emptying phenomenon, orbital debris of non-dimensional alumina. negligible (ie> to a few millimeters).
- aluminized solid propellants which, by combustion, produce small diameter alumina (thus promoting the reduction of thrust oscillations in solid propellant propellants and having the combined positive effect of reducing the deposit in the rear bottom of the nozzle) while maintaining ballistic properties, including combustion rates, similar to those of industrial propellants for space application known to date.
- the results of granulometric measurements of a particle size class are expressed in the form of curves, giving: on the one hand, the histogram of the volume percentages of particles (also called percentages of passing volume) as a function of the diameter (equivalent spherical) of the particles and, on the other hand, the cumulation of the voluminal percentages of particles as a function of the diameter (equivalent spherical) of the particles, cumulated carried out according to the increasing diameters.
- Dso diameter for which the cumulative volume percentage is equal to 50%
- a particle size class of a particulate material is defined by its particle size envelope defined by minimum and maximum values of D 10, D 50, D 90 .
- the present invention relates to solid propellants:
- the Applicant has been able to select and associate different granulometries (monomodal) of ammonium perchlorate, so that, during the combustion of the propellant, the agglomeration of the aluminum in combustion is limited, in order to reduce, or almost to remove, the production of particles larger than 10 microns diameter, while maintaining the standard values of the ballistic parameters for a propulsive space application.
- the present invention firstly relates to a process for obtaining a composite solid propellant, said process comprising: - obtaining a paste by mixing, in a mixer, a mixture containing a liquid polyol polymer (generally present in the mixture, at 5 to 15% by weight, more generally at 7 to 14% by weight), an oxidizing charge of ammonium perchlorate (generally present in the mixture at a rate of 40 to 80% by weight).
- a reducing charge of aluminum generally present in the mixture at a rate of 15 to 20% by weight, more generally at a rate of 16 to 19% in bulk
- said oxidizing charge of ammonium perchlorate in said paste results from the introduction into said mixer, separately or as a mixture, of at least:
- class A a first charge whose monomodate granulometric distribution (called class A) has a Dio value between 100 ⁇ m and 10 ⁇ m, a D 5 o value between 170 ⁇ m and 220 ⁇ m and a value of D 9 $ between 315 ⁇ m and 340 ⁇ m, and
- class B a second charge whose monomodal particle size distribution (called class B) has a Di 0 value between 15 ⁇ m and 20 ⁇ m, a Ds 0 value between 60 ⁇ m and 120 ⁇ m and a D 90 value between 185 ⁇ m and 220 ⁇ m; and eventually,
- class C a third charge whose monomodal particle size distribution (called class C) has a Dio value of between 1.7 ⁇ m and 3.6 ⁇ m, a D 50 value of between 6 ⁇ m and 12 ⁇ m and a Dgo value of between between 20 ⁇ m and 32 ⁇ m.
- the method of the invention is a method by analogy which comprises, in a conventional manner, obtaining a paste from the constituent ingredients of the propellant referred to, casting said paste in a mold and its crosslinking by heat treatment (baking ).
- the ingredients involved are the classic ingredients for this type of propellant. They understand :
- liquid polyol polymer preferably, said polyol polymer is a hydroxytelechelic polybutadiene;
- PA ammonium perchlorate
- said at least one crosslinking agent (generally liquid) of said polyol polymer: said at least one crosslinking agent (at least bifunctional) is generally chosen from polyisocyanates, it preferably consists of an aliphatic polyisocyanate. It advantageously consists of cyclohexylmethylene diisocyanate (MCDI);
- said at least one plasticizer is preferably chosen from dioctyl azéiate (DOZ), sebacate of isooctyl, isodecyl pelargonate, polyisobutylene, dioctyl phthalate (DOP);
- DOZ dioctyl azéiate
- DOP dioctyl phthalate
- said at least one additive may in particular consist of one or more adhesion agents between the binder and the oxidizing filler, such as, for example, bis (2-methylaziridinyl) -methylaminophosphine oxide (methyl BAPO) or triethylene pentamine acrylonitrile (TEPAN), in one or more antioxidant agents derived from those of the rubber industry, such as, for example, ditertiobutylparacresol (DBC) or 2,2'-methylenebis (4-methyl-6-tertio) ⁇ butylphenol) (MBP5), in one or more crosslinking catalysts, such as iron or copper acetylacetonate, tin dibutyldilaurate (DBTL), in one or more combustion catalysts, such as iron oxide , ...
- adhesion agents between the binder and the oxidizing filler such as, for example, bis (2-methylaziridinyl) -methylaminophosphine oxide (methyl BAPO) or triethylene pent
- the charge of ammonium perchlorate is, in the context of the process of the invention, optimized: it is obtained from at least a first and second (or even third) charges having , each, a monomodal particle size distribution as specified above. It results, typically, from the introduction, in the mixer, separately or in mixture, of at least two charges of different monomodal granulometry: the first of class A (see above) and the second of class
- the charge of ammonium perchlorate of the mixture, in the mixer is at least partly advantageously in its entirety, constituted from a first and second charges (each) of specific monomodal particle size, or even a first, second and third charge (each) of specific monomodafe particle size.
- the mixture (binary or ternary) of the first and second or first, second and third oxidizing charges of different specific monomodal granulometry can be performed upstream.
- the oxidizing charge of the propellant is carried out upstream and is then added, pre-constituted, in the mixer.
- the mixture (binary or ternary) of the first and second or first, second and third oxidizing charges of different specific monomodal granulometry may be carried out only in the mixer within the dough. According to this variant, it is not pre-constituted. The first, second or even third charges can thus be introduced separately. In the context of this variant, when three types of oxidizing charges are introduced, it is however possible to preconstitute a mixture (binary), first and second, first and third, or second and third, oxidizing charges of specific monomodal particle size. Then added to the mixer "said mixture and, respectively, the third, the second, or the first, oxidizing charge (complementary oxidizing charge) so that said first, second and third fillers constitute the oxidizing charge of the propellant.
- the oxidizing charge of ammonium perchlorate in the dough results only from the introduction into the mixer (separately or in mixture) of the first and the second charge, the monomodal particle size of which has been specified above. (using the value ranges of D I Q, DS ⁇ and D 90 ).
- oxidizing charge of ammonium perchlorate (100%) in the paste results, generally, from the introduction into the mixer, separately or as a mixture, of:
- the oxidizing charge of ammonium perchlorate (100%) in the paste results, very generally, from the introduction into the mixer, separately or as a mixture, of;
- the oxidizing charge of ammonium perchlorate (100%) in the paste results, preferably, from the introduction into the mixer, separately or as a mixture, of:
- the particle size of the aluminum charge is a second-order parameter, with reference to the technical problems mentioned above.
- the aluminum particles generally have a median diameter of less than or equal to 40 ⁇ m. The best results, up to the production of alumina of monomodal granulometry centered to 1 to 3 ⁇ m, are obtained with aluminum particles having a median diameter of between 1 and 10 ⁇ m and certain combinations of ammonium perchlorate of class A and B (see examples below) introduced into the mixer to form the ammonium perchlorate charge.
- Said aluminum filler therefore generally has a median diameter (D 50 ) less than or equal to 40 ⁇ m, advantageously between 1 and 10 ⁇ m.
- D 50 median diameter
- D 10 and D 90 of said aluminum charge advantageously correspond, respectively, to at least 1/4 and at most 4 times said median diameter
- the present invention relates to aluminized solid propellants obtainable by the above process, which process involves oxidizing ammonium perchlorate charges of different specific monomodal particle sizes.
- the solid propellants of the invention generally have combustion rates of between 6 and 12 mm / s and pressure exponents of between 0.15 and 0.4, advantageously between 0.2 and 0.4, over a range of operating pressure of 3 to 10 MPa, which corresponds to the standard values of the ballistic parameters.
- the great advantage of the method of the invention is thus to allow the production of solid propellants which have such ballistic properties and whose combustion generates particles of alumina of small grain size,
- the granulometry of the alumina produced by the combustion of the propellants of the invention was determined by means of measuring equipment, recognized by the international community, as "rotary trap or" Quench Party of Combustion Bomb ". by Norton Thiokol (see PC BRAITHWAITE, WN CHRISTENSEN, V. DAUGHERTY (Morton Thiokol), Quench bomb investigation of aluminum oxide formation from solid rocket propellants (part I): experimental metbodology, 25th JANNAF combustion meeting, CPIA Publication 498, vol.l, p. 175, October 1988).
- the principle is to burn a small sample of propellant at the end of a fixed rod in a chamber at room temperature pressurized, in general, with nitrogen.
- a bowl containing alcohol rotates around the sample. The distance between the sample and the alcohol film formed in the wall of the bowl is adjustable. Most drops ejected from the burning surface impart the rotating liquid. After the test, the liquid is recovered and the particles analyzed.
- the particle size distribution, by volume, of the recovered particles is then measured by means of a photon correlation optical particle size analyzer (PCS-DLS, Photons Correlation Spectroscopy-Diffusion Light Scattering).
- PCS-DLS Photons Correlation Spectroscopy-Diffusion Light Scattering
- the solid propellants of the invention produce, during their combustion, particles of smaller dimensions than those produced by the propellant combustion of the same type of the prior art.
- the percentage of the total volume (passing) corresponding to particles of diameter (spherical equivalent) greater than 10 ⁇ m is thus less than 15%, generally between 2% and 10%, for the propellants of the invention, much lower than that reference propellants of the prior art ( ⁇ 30%).
- the grain size curves of the particles produced by the combustion of the propellants of the invention always show, like those of the propellants of the prior art, a particle size peak centered on approximately 0.1 to 3 ⁇ m.
- a second particle size peak corresponding to particles of diameter greater than 10 microns. This second peak is centered at 10 to 50 ⁇ m for the propellants of the invention, values lower than those (60 to 100 ⁇ m) observed for propellants of the prior art.
- the preferred propellants of the invention do not exhibit said second particle size peak and therefore only produce a residual percentage of particles with a diameter greater than 10 ⁇ m.
- the invention relates to a solid propellant charge containing a solid propellant of the invention. According to yet another of its objects, the invention relates to a rocket engine comprising at least one load containing a propellant of the invention.
- the invention finally relates to an oxidizing charge of ammonium perchlorate, in particular useful for the implementation of the method for obtaining a composite solid propellant of the invention as described above, in particular useful for obtaining a composite solid propellant of the invention as described above, said charge is obtainable by mixing at least two charges selected from the first, second and third charges as defined above ( binary or ternary mixtures), advantageously obtainable by mixing at least a first charge and at least a second charge (binary mixtures) and optionally at least a third charge (ternary mixtures) as defined herein. above, very advantageously capable of being obtained by mixing at least a first charge and at least a second charge (binary mixtures) as defined above. It advantageously contains said feeds in the weight proportions specified above.
- Figure 1 shows a diagram of the combustion of a drop of aluminum.
- FIG. 2 illustrates the phenomena producing the different alumina granulometries generated during the combustion of a solid propellant.
- FIG. 3 shows the volume particle size curves, measured by means of a photon correlation optical particle size analyzer (PCS-DLS: Photons Correlation Spectroscopy-Diffusion Light Scattering), particles produced by the preferred propellant according to the invention (see FIG. Example 9 below) in comparison with those produced with a reference propellant of prior art (see below).
- PCS-DLS Photons Correlation Spectroscopy-Diffusion Light Scattering
- Table 1 below gives the mass percentages of the constituents (PA, AI) of solid propellants according to the invention, the ballistic properties of said propellants as well as the particle sizes of the alumina produced during the combustion of said propellants. These same data are given for three reference propellants.
- the solid propellants of Table 1 are solid polyurethane-bonded composite propellants and contain an oxidizing charge of ammonium perchlorate and an aluminum charge.
- Reference propellants 1 and 2 have a conventional composition. They are of the type used for space applications.
- the reference propellant 3 shows the influence of the strong presence (42%) of small particles of ammonium perchlorate on the rate of combustion (logically small alumina particles are then obtained).
- the solid propellants of the invention according to Examples 1 to 12 have combustion rates and pressure exponents measured at 5 MPa in the expected speed and exponent ranges for the targeted range of application, close to those of the reference propellots. 1 and 2.
- the last line of Table 1 relates to the propellant M 12 of Table 3 of Massa et al. (Journal of Propulsion and Power, Vol 24, No. 2,
- the alumina particles produced by the solid propellants of the Table 1 was recovered using a pressurized chamber equipped with a trapping means (test means "rotary trap described above) .
- the procedure for capturing the particles is as follows;
- the alcohol contained in the rotary trap is plated, in the form of a film (about 2 mm thick), on the side walls of the bowl, by rotating of the last ;
- the pressure inside the chamber is set to 5 MPa relative. Pressurization is carried out by nitrogen and the distance between the propellant sample and the alcohol film is 20 mm from the combustion. The emitted particles are taken horizontally;
- the free face of the propellant cube facing the alcohol film is lit (the very short duration of the combustion makes it possible to maintain an almost constant combustion surface).
- the principle of recovery consists in recovering in the alcohol the condensed phase particles emitted in the combustion gases of the propellant sample.
- PCS-DLS Photons Correlation Spectroscopy-Diffusion Light Scattering
- the particle size distribution or distribution of the particles collected in ethanol during the combustion of the propellant is expressed in the form of two curves; on the one hand, the histogram giving the volume fraction of the particles as a function of the class of equivalent spherical diameter of the particles analyzed, and, on the other hand, the curve giving the cumulated volume fraction as a function of the class of equivalent spherical diameter particles analyzed.
- FIG. 3 shows the curves obtained for the reference propellant i and that of example 9 according to the invention.
- Table 1 shows the characteristic values recorded on the particle size curves of the recovered particles produced by the combustion of the reference solid propellants and examples according to the invention (see the last three columns of Table 1).
- compositions of the solid propellants of Table 1 are given by the mass percentage of the ammonium perchlorate charge and the constitution of this charge (class A / B / C), the mass percentage of aluminum and its particle size class (specified in Table 2), the complement to 100% of the mass consisting of the polymer polyol polybutadiene hydroxytelechelic PBHT R45HTLO sold by the company Sartomer, the crosslinking agent MDCI, the plasticizer DOZ and additives.
- the particle size histograms always have at least one granulometric peak for diameters of less than 10 ⁇ m.
- the values given in the column "Dpkx10 ⁇ m" in Table 1 correspond to the value or the range of values (when there are several peaks, or when a dispersion of the values is measured over several tests) of the maximum said at least one granulometric peak for diameters less than 10 ⁇ m measured.
- the granulometric curve furthermore has a particle size peak for particles with a diameter of greater than 10 ⁇ m, the value or the range of values recorded (for example taken from several tests) of the diameter of the maximum of said particle size peak for particles with a diameter larger than 10 ⁇ m. 10 ⁇ m is indicated in the column "DpiolO ⁇ m" of Table 1.
- the solid propellants of the invention produce a reduced amount of alumina particles larger than 10 ⁇ m in diameter, relative to the reference propellants 1 and 2. This is expressed in Table 1 by the value of the volume percentage (volume passing up on the curve giving the cumulative volume fraction as a function of the equivalent spherical diameter class of the particles analyzed) corresponding to the classes of particles with a diameter greater than 10 ⁇ m. All the propellants of the invention lead to a passing volume percentage corresponding to particles of diameter greater than 10 microns much lower than that of the reference propellant.
- Said propellant M12 has a combustion rate of 14 mm / s at 4 MPa ( Figure 12c). As the burning speed of the solid propellants increases with the pressure, the burning rate of the M12 propellant at a pressure of 5 MPa (reference pressure for the examples of the invention) can only be greater than this value of 14 mm / s. It is therefore much higher than those of the reference propellants 1 and 2.
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0954501A FR2947543B1 (fr) | 2009-07-01 | 2009-07-01 | Procede d'obtention de propergols solides composites aluminises ; solides composites aluminises |
PCT/FR2010/051364 WO2011001107A1 (fr) | 2009-07-01 | 2010-06-29 | Procede d'obtention de propergols solides composites aluminises; propergols solides composites aluminises |
Publications (2)
Publication Number | Publication Date |
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EP2448885A1 true EP2448885A1 (de) | 2012-05-09 |
EP2448885B1 EP2448885B1 (de) | 2018-11-28 |
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EP10745374.8A Active EP2448885B1 (de) | 2009-07-01 | 2010-06-29 | Verfahren zur herstellung von festen zusammengesetzten aluminisierten treibstoffen und feste zusammengesetzte aluminisierte treibstoffe |
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US (1) | US20120079807A1 (de) |
EP (1) | EP2448885B1 (de) |
JP (1) | JP5773450B2 (de) |
KR (1) | KR101768440B1 (de) |
CN (1) | CN102471175B (de) |
BR (1) | BRPI1010746B1 (de) |
FR (1) | FR2947543B1 (de) |
IL (1) | IL217162A (de) |
RU (1) | RU2535224C2 (de) |
WO (1) | WO2011001107A1 (de) |
Families Citing this family (9)
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KR101296690B1 (ko) * | 2013-03-14 | 2013-08-19 | 엘아이지풍산프로테크(주) | 열가소성 바인더를 사용하여 형상 변형이 가능한 혼합형 고체 추진제 조성물 |
FR3007758B1 (fr) * | 2013-06-28 | 2015-10-09 | Herakles | Propergol solide composite dont la charge reductrice d'aluminium renferme un faible taux de magnesium |
CN103674644B (zh) * | 2013-12-10 | 2015-09-30 | 哈尔滨工程大学 | 一种铝冰固体推进剂试件的制作装置 |
FR3017615B1 (fr) * | 2014-02-18 | 2016-03-11 | Herakles | Chargements de propergol solide optimises pour limiter les instabilites thermo-acoustiques ; moteurs de fusee associes |
CN105130720B (zh) * | 2014-05-30 | 2017-11-14 | 湖北航天化学技术研究所 | 一种高能低燃速温度敏感系数推进剂 |
CN105840344B (zh) * | 2016-04-20 | 2017-12-08 | 哈尔滨工业大学 | 一种固体火箭发动机内孔燃烧药柱制备及安全快速脱模工艺 |
CN108530239B (zh) * | 2018-06-29 | 2020-08-14 | 湖北航天化学技术研究所 | 一种高固体含量nepe固体推进剂浆料、推进剂及制备方法 |
CN110041153A (zh) * | 2019-03-22 | 2019-07-23 | 山西北方兴安化学工业有限公司 | 一种双层管状组合推进剂药柱螺压包覆模具 |
FR3102476B1 (fr) | 2019-10-24 | 2021-11-26 | Arianegroup Sas | Propergol solide composite |
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US3795106A (en) | 1972-07-07 | 1974-03-05 | Rockwell International Corp | Baffled solid propellant motor |
EP0238210A3 (en) * | 1986-03-14 | 1989-05-24 | Imperial Chemical Industries Plc | Solid explosive composition |
US5112417A (en) * | 1991-05-20 | 1992-05-12 | United States Of America | Method of controlling the increase in potlife of propellants during processing |
JPH0794359B2 (ja) * | 1991-11-01 | 1995-10-11 | 旭化成工業株式会社 | 過塩素酸アンモニウムコンポジット推進薬 |
US5771679A (en) * | 1992-01-29 | 1998-06-30 | Thiokol Corporation | Aluminized plateau-burning solid propellant formulations and methods for their use |
US5334270A (en) * | 1992-01-29 | 1994-08-02 | Thiokol Corporation | Controlled burn rate, reduced smoke, solid propellant formulations |
JPH07133180A (ja) * | 1993-11-09 | 1995-05-23 | Daicel Chem Ind Ltd | ガス発生剤組成物 |
FR2728562B1 (fr) * | 1994-12-22 | 1997-01-24 | Poudres & Explosifs Ste Nale | Procede de fabrication en continu de chargements pyrotechniques a liant silicone et compositions susceptibles d'etre mises en oeuvre par ce procede |
FR2764645B1 (fr) | 1997-06-16 | 1999-08-20 | Aerospatiale | Chargement de propergol solide pour propulseur et propulseur muni d'un tel chargement |
WO1999018051A2 (en) * | 1997-10-03 | 1999-04-15 | Cordant Technologies, Inc. | High pressure, high performance solid rocket hydroxy-terminated polybutadiene propellant formulations |
US6503350B2 (en) * | 1999-11-23 | 2003-01-07 | Technanogy, Llc | Variable burn-rate propellant |
US6679959B2 (en) * | 2000-12-18 | 2004-01-20 | The United States Of America As Represented By The Secretary Of The Navy | Propellant |
FR2844557B1 (fr) | 2002-09-12 | 2006-03-03 | Snecma Propulsion Solide | Systeme et procede de controle des oscillations de pression d'origine hydrodynamique pour propulseur a propergol solide |
US7011722B2 (en) * | 2003-03-10 | 2006-03-14 | Alliant Techsystems Inc. | Propellant formulation |
US6979022B2 (en) * | 2003-05-23 | 2005-12-27 | Autoliv Asp, Inc. | Flexible inflator with co-extruded propellant and moisture barrier |
RU2258057C2 (ru) * | 2003-10-28 | 2005-08-10 | Процун Евгений Григорьевич | Смесевое твердое ракетное топливо |
JP5041467B2 (ja) * | 2007-01-11 | 2012-10-03 | 防衛省技術研究本部長 | コンポジット推進薬 |
-
2009
- 2009-07-01 FR FR0954501A patent/FR2947543B1/fr not_active Expired - Fee Related
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2010
- 2010-06-29 BR BRPI1010746A patent/BRPI1010746B1/pt active IP Right Grant
- 2010-06-29 WO PCT/FR2010/051364 patent/WO2011001107A1/fr active Application Filing
- 2010-06-29 JP JP2012519034A patent/JP5773450B2/ja active Active
- 2010-06-29 EP EP10745374.8A patent/EP2448885B1/de active Active
- 2010-06-29 RU RU2012102072/05A patent/RU2535224C2/ru active
- 2010-06-29 US US13/377,767 patent/US20120079807A1/en not_active Abandoned
- 2010-06-29 CN CN201080030001.0A patent/CN102471175B/zh active Active
- 2010-06-29 KR KR1020127002879A patent/KR101768440B1/ko active IP Right Grant
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2011
- 2011-12-22 IL IL217162A patent/IL217162A/en active IP Right Grant
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Also Published As
Publication number | Publication date |
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FR2947543A1 (fr) | 2011-01-07 |
IL217162A (en) | 2016-04-21 |
BRPI1010746B1 (pt) | 2020-05-05 |
KR20120095841A (ko) | 2012-08-29 |
US20120079807A1 (en) | 2012-04-05 |
BRPI1010746A2 (pt) | 2017-05-16 |
CN102471175A (zh) | 2012-05-23 |
IL217162A0 (en) | 2012-02-29 |
CN102471175B (zh) | 2014-11-05 |
RU2535224C2 (ru) | 2014-12-10 |
FR2947543B1 (fr) | 2012-06-15 |
EP2448885B1 (de) | 2018-11-28 |
JP2012531380A (ja) | 2012-12-10 |
KR101768440B1 (ko) | 2017-08-16 |
WO2011001107A1 (fr) | 2011-01-06 |
RU2012102072A (ru) | 2013-08-10 |
JP5773450B2 (ja) | 2015-09-02 |
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