Polymer-bonded explosive

Polymer-bonded explosives have several potential advantages: • If the polymer matrix is an elastomer (rubbery material), it tends to absorb shocks, making the PBX very insensitive to accidental detonation, and thus ideal for insensitive munitions. • Hard polymers can produce PBX that is very rigid and maintains a precisely engineered 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, a billet of PBX can be precisely shaped on a lathe or CNC machine. This technique is used to machine explosive lenses necessary for modern nuclear weapons. == Binders ==

Fluoropolymers Fluoropolymers are advantageous as binders due to their high density (yielding high detonation velocity) and inert chemical behavior (yielding long shelf stability and low aging). They are somewhat brittle, as their glass 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. == Insults (potential explosive inhibitors) ==

Explosive yields can be affected by the introduction of mechanical loads or the application of temperature; such damages are called insults. The mechanism of a thermal insult at low temperatures on an explosive is primarily thermomechanical, at higher temperatures it is primarily thermochemical. Thermomechanical 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, and phase 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 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. by Ostwald 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. == Some example PBXs ==