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Polymer-bonded explosive

From Wikipedia, the free encyclopedia
Explosive materials where powder is bound together in a matrix with synthetic polymer
Not to be confused withplastic explosive.

Polymer-bonded explosives, also calledPBX orplastic-bonded explosives, areexplosive materials in which explosive powder is bound together in a matrix using small quantities (typically 5–10% by weight) of a syntheticpolymer. PBXs are normally used for explosive materials that are not easily melted into a casting, or are otherwise difficult to form.

PBX was first developed in 1952 atLos Alamos National Laboratory, asRDX embedded inpolystyrene withdiisooctyl phthalate (DEHP)plasticizer.HMX compositions withteflon-based binders were developed in 1960s and 1970s forgun shells and forApollo Lunar Surface Experiments Package (ALSEP)seismic experiments,[1] although the latter experiments are usually cited as usinghexanitrostilbene (HNS).[2]

Potential advantages

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Polymer-bonded explosives have several potential advantages:

  • If the polymer matrix is anelastomer (rubbery material), it tends to absorb shocks, making the PBX very insensitive to accidental detonation, and thus ideal forinsensitive munitions.
  • Hard polymers can produce PBX that is very rigid and maintains a precise engineering shape even under severe stress.
  • PBX powders can be pressed into a desired shape at room temperature; casting normally requires hazardous melting of the explosive. High pressure pressing can achieve density for the material very close to the theoretical crystal density of the base explosive material.
  • Many PBXes are safe to machine; turning solid blocks into complex three-dimensional shapes. For example, abillet of PBX can be precisely shaped on alathe orCNC machine. This technique is used to machineexplosive lenses necessary for modern nuclear weapons.[3]

Binders

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Fluoropolymers

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Main article:Fluoropolymer

Fluoropolymers are advantageous as binders due to their highdensity (yielding highdetonation velocity) and inert chemical behavior (yielding long shelf stability and lowaging). They are somewhat brittle, as theirglass transition temperature is at room temperature or above. This limits their use to insensitive explosives (e.g.TATB) where the brittleness does not have detrimental effects on safety. They are also difficult to process.[4]

Elastomers

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Main article:Elastomer

Elastomers have to be used with more mechanically sensitive explosives likeHMX. The elasticity of the matrix lowers sensitivity of the bulk material to shock and friction; their glass transition temperature is chosen to be below the lower boundary of the temperature working range (typically below -55 °C).Crosslinkedrubber polymers are however sensitive to aging, mostly by action offree radicals and byhydrolysis of the bonds by traces of water vapor. Rubbers likeEstane orhydroxyl-terminated polybutadiene (HTPB) are used for these applications extensively.Silicone rubbers andthermoplastic polyurethanes are also in use.[4]

Fluoroelastomers, e.g.Viton, combine the advantages of both.

Energetic polymers

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Energetic polymers (e.g. nitro or azido derivates of polymers) can be used as a binder to increase the explosive power in comparison with inert binders.Energetic plasticizers can be also used. The addition of a plasticizer lowers the sensitivity of the explosive and improves its processibility.[1]

Insults (potential explosive inhibitors)

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Explosive yields can be affected by the introduction of mechanical loads or the application of temperature; such damages are calledinsults. The mechanism of a thermal insult at low temperatures on an explosive is primarily thermomechanical, at higher temperatures it is primarily thermochemical.

Thermomechanical

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Thermomechanical mechanisms involve stresses by thermal expansion (namely differential thermal expansions, as thermal gradients tend to be involved), melting/freezing or sublimation/condensation of components, andphase transitions of crystals (e.g. transition of HMX from beta phase to delta phase at 175 °C involves a large change in volume and causes extensive cracking of its crystals).

Thermochemical

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Thermochemical changes involve decomposition of the explosives and binders, loss of strength of binder as it softens or melts, or stiffening of the binder if the increased temperature causes crosslinking of the polymer chains. The changes can also significantly alter the porosity of the material, whether by increasing it (fracturing of crystals, vaporization of components) or decreasing it (melting of components). The size distribution of the crystals can be also altered, e.g. byOstwald ripening. Thermochemical decomposition starts to occur at the crystal nonhomogeneities, e.g. intragranular interfaces between crystal growth zones, on damaged parts of the crystals, or on interfaces of different materials (e.g. crystal/binder). Presence of defects in crystals (cracks, voids, solvent inclusions...) may increase the explosive's sensitivity to mechanical shocks.[4]

Some example PBXs

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Some example PBXs
NameExplosive ingredientsInert ingredientsUsage
AFX-757RDX 25%, ammonium perchlorate 30%, aluminium 33%HTPB 4.44%, dioctyl adipate 6.56%Used in warheads forJASSM,GBU-39 Small Diameter Bomb and similar weapons.[5] Has high air blast equivalent, 1.39 times more thanComposition B, but low brisance due to low high explosive content.[6][7]
EDC-8PETN 76%RTV silicone 24%[8]
EDC-28RDX 94%FPC 461 6%[9]
EDC-29β-HMX 95%HTPB 5%UK composition[4]
EDC-32HMX 85%15% Viton A 15%[9]
EDC-37HMX 91%,NC 1%K-10 liquid 8%[9]
LX-04HMX 85%Viton-A 15%High-velocity;nuclear weapons (W62,W70)[9]
LX-07HMX 90%Viton-A 10%High-velocity;nuclear weapons (W71)[9]
LX-08PETN 63.7%Sylgard 182 (silicone rubber) 34.3%, 2% Cab-O-Sil[10]
LX-09-0HMX 93%2,2-dinitropropyl acrylate (pDNPA) 4.6%; FEFO 2.4%High-velocity;nuclear weapons (W68). Prone to deterioration and separation of theplasticizer andbinder. Caused serious safety problems. FEFO is 1,1-[methylenebis(oxy)]-bis-[2-fluoro-2,2-dinitroethane], liquid explosive.[3]
LX-09-1HMX 93.3%pDNPA 4.4%; FEFO 2.3%
LX-10-0HMX 95%Viton-A 5%High-velocity;nuclear weapons (W68 (replaced LX-09),W70,W79,W82)[9]
LX-10-1HMX 94.5%Viton-A 5.5%
LX-11-0HMX 80%Viton-A 20%High-velocity;nuclear weapons (W71)
LX-14-0HMX 95.5%Estane & 5702-Fl 4.5%[9]
LX-15HNS 95%Kel-F 800 5%
LX-16PETN 96%FPC461 4%FPC461 is avinyl chloride:chlorotrifluoroethylene copolymer and its response to gamma rays has been studied.[11]
LX-17-0TATB 92.5%Kel-F 800 7.5%High-velocity,insensitive;nuclear weapons (B83,W84,W87,W89)
PBX 9007RDX 90%Polystyrene 9.1%;DOP 0.5%;rosin 0.4%[9]
PBX 9010RDX 90%Kel-F 3700 10%High-velocity;nuclear weapons (W50,B43)[9]
PBX 9011HMX 90%Estane and 5703-Fl 10%High-velocity;nuclear weapons (B57 mods 1 and 2)[9]
PBX 9205RDX 92%Polystyrene 6%;DOP 2%Created in 1947 at Los Alamos, later given the PBX 9205 designation.[12]
PBX 9404HMX 94%,NC 3%Tris(b-chloroethyl)phosphate (CEF) 3%High-velocity;nuclear weapons, widely used (B43,W48,W50,W55,W56,B57 mod 2,B61 mods 0, 1, 2, 5,W69). Serious safety problems related to aging and decomposition of the nitrocellulose binder.[13]
PBX 9407RDX 94%FPC461 6%[9]
PBX 9501HMX 95%, BDNPA-F 2.5%Estane 2.5%High-velocity;nuclear weapons (W76,W78,W88). One of the most extensively studied high explosive formulations.[4] BDNPA-F is 1:1 mixture of bis(2,2-dinitropropyl) acetal and bis(2,2-dinitropropyl) formal.[3]
PBS 9501-Estane 2.5%; BDNPA-F 2.5%; sieved white sugar 95%Inert simulant of mechanical properties of PBX 9501[4]
PBX 9502TATB 95%Kel-F 800 5%High-velocity,insensitive; principal in recent USnuclear weapons (B61 mods 3, 4, 6–10,W80,W85,B90,W91), backfitted to earlier warheads to replace less safe explosives.[9]
PBX 9503TATB 80%;HMX 15%Kel-F 800 5%Also known as X-0351.[9]
PBX 9604RDX 96%Kel-F 800 4%
PBXN-101HMX 82%
PBXN-102HMX 59%, Aluminum 23%
PBXN-103Ammonium perchlorate (AP) 40%, Aluminum 27%,TMETN 23%TEGDN 2.5%Mk 48 torpedoes
PBXN-104HMX 70%
PBXN-105RDX 7%, AP 49.8%, Aluminum 25.8%
PBXN-106RDX 75%polyethylene glycol/BDNPA-F binderNaval shells
PBXN-107RDX 86%polyacrylate binderBGM-109 Tomahawk missiles
PBXN-109RDX 64%, Aluminum 20%HTPB, DOA (dioctyladipate), and IPDI (isophorone diisocyanate)Used in some versions of theMark 82,Mark 83 andMark 84 general-purpose bombs.[14]
PBXN-110HMX 88%5.4% Polybutadiene, 5% Isodecylpelargonate[15]
PBXN-111RDX 20%, AP 43%, Aluminum 25%
PBXW-114HMX 78%, Aluminum 10%
PBXW-115RDX 20%, AP 43%, Aluminum 25%
PBXN-1RDX 68%, Aluminum 20%
PBXN-3RDX 85%NylonAIM-9X Sidewinder Missile
PBXN-4Diaminotrinitrobenzene (DATB) 94%
PBXN-5HMX 95%fluoroelastomer 5%Naval shells
PBXN-6RDX 95%
PBXN-7RDX 35%, TATB 60%
PBXN-9HMX 92%HYTEMP 4454 2%,Diisooctyl adipate (DOA) 6%
XTX 8003PETN 80%Sylgard 182 (silicone rubber) 20%High-velocity, extrudable;nuclear weapons (W68,W76)[15]
XTX 8004RDX 80%Sylgard 182 (silicone rubber) 20%[15]

References

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  1. ^abAkhavan, Jacqueline (2004-01-01).The Chemistry of Explosives (2nd ed.). Royal Society of Chemistry.ISBN 978-0-85404-640-9.Archived from the original on 2023-02-15. Retrieved2021-12-13.
  2. ^James R.Bates; W.W.Lauderdale; Harold Kernaghan (April 1979)."ALSEP (Apollo Lunar Surface Experiments Package) Termination Report"(pdf-8.81 mb). NASA-Scientific and Technical Information Office.Archived(PDF) from the original on 2010-01-13. Retrieved2014-06-29.
  3. ^abcCarey Sublette (1999-02-20)."4.1.6.2.2.5 Explosives".4. Engineering and Design of Nuclear Weapons: 4.1 Elements of Fission Weapon Design. Retrieved2010-02-08.
  4. ^abcdefBlaine Asay, ed. (2009).Non-Shock Initiation of Explosives. Springer Berlin Heidelberg.ISBN 978-3-540-88089-9.
  5. ^Sweeney, Kevin P. (August 2016).Miniature Munitions: Is The US Military Prepared to Support Major Combat Operations(PDF) (Thesis). Air Command and Staff College, Air University.S2CID 115831591.
  6. ^Kolev, Stefan K.; Tsonev, Tsvetomir T. (2022). "Aluminized Enhanced Blast Explosive Based on Polysiloxane Binder".Propellants, Explosives, Pyrotechnics.47 (2).doi:10.1002/prep.202100195.S2CID 244902961.
  7. ^US patent 6523477B1, George W. Brooks & Eric E. Roach, "Enhanced Performance Insensitive Penetrator Warhead", issued 2003-02-25, assigned to Lockheed Martin Corporation 
  8. ^Technical Area 36 Open Detonation Unit — SUPPLEMENT 2-1 Waste Explosives Detonated at Technical Area 36(PDF) (Report). September 1999. p. 2.Archived(PDF) from the original on 2022-10-01.
  9. ^abcdefghijklmTechnical Area 36 Open Detonation Unit — SUPPLEMENT 2-1 Waste Explosives Detonated at Technical Area 36, p. 2.
  10. ^H K Otsuki; E Eagan-McNeill (May 1997).A Blue Print for Building a Risk Assessment (Report). Lawrence Livermore National Laboratory. p. 6. UCRL-JC-127467.Archived from the original on 2022-09-29.
  11. ^Sarah C. Chinn; Thomas S. Wilson; Robert S. Maxwell (March 2006)."Analysis of radiation induced degradation in FPC-461 fluoropolymers by variable temperature multinuclear NMR".Polymer Degradation and Stability.91 (3):541–547.doi:10.1016/j.polymdegradstab.2005.01.058.Archived from the original on 2022-04-17. Retrieved2019-09-09.
  12. ^Anders W. Lundberg."High Explosives in Stockpile Surveillance Indicate Constancy"(PDF). Lawrence Livermore National Laboratory (LLNL).Archived(PDF) from the original on 2012-10-10. Retrieved2014-03-02.
  13. ^Kinetics of PBX 9404 AgingArchived 2017-02-11 at theWayback Machine Alan K. Burnhamn; Laurence E. Fried. LLNL, Unclassified, 2007-04-24 (pdf)
  14. ^Janes (26 July 2022),"Mk 80 general-purpose bombs (BLU-110/111/117/126/129)",Janes Weapons: Air Launched,Coulsdon,Surrey: Jane's Group UK Limited., retrieved29 May 2023
  15. ^abcTechnical Area 36 Open Detonation Unit — SUPPLEMENT 2-1 Waste Explosives Detonated at Technical Area 36, p. 3.
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