In this work, 1,3,5‐trinitroperhydro‐1,3,5‐triazine (RDX) with an average crystal size of 300 nm was prepared by bead milling to examine the effect of pH and ionic strength on the Zeta potential. The results showed that nanoRDX has no isoelectric point within the entire range studied (2
Wetting behavior of energetic materials surface including cyclotrimethylene trinitramine (RDX), cyclotetramethylene tetranitramine (HMX) and hexanitrohexaazaisowurtzitane (CL-20) using nonionic (Triton-X), anionic (SDS), and cationic (TTAB) surfactants has been studied by contact angle tensiometry. Results show that TTAB more significantly reduces the contact angle and improves wettability as compared to SDS and Triton-X. The liquid-vapor surface tension g lv was measured as a function of TTAB surfactant concentration in aqueous solutions and used to construct a Zisman plot to determine the critical surface tension of RDX, HMX and CL-20. The results show that HMX displays the highest degree of wettability while RDX is most difficult to wet.The computed values of the work of spreading complement the previously discussed results where contact angle decreases with increasing surfactant concentration. They also indicate that RDX appears most impacted by the addition of TTAB surfactant. However, the addition of TTAB also has a significant impact on improving the wettability of HMX and CL-20. This wettability study plays an important role in the formation of well-wetted energetic surfaces needed for efficient wet milling, coating and granulation processes.
The focus of this paper is to investigate the polymeric stabilization of cyclotetramethylene tetranitramine (HMX) suspensions using polyvinylpyrrolidone (PVP). The PVP adsorption on HMX surface was studied using zeta potential measurements, which revealed that the shorter PVP polymer chain (lesser molecular weight) adsorbed better than the longer one (greater molecular weight). This study also showed that the solvent dramatically affects the PVP adsorption. A turbidity test was conducted, showing that lower molecular weight PVP offers better stability. This stability is enhanced by increasing the ethanol concentration. The depletion mechanism was responsible for HMX stabilization with ethanol. Finally, a milling study was conducted to compare the HMX with and without a stabilization mechanism. This study indicated that PVP in 50 % water/50 % ethanol was able to stabilize HMX by depletion and reduce the size to 180 nm within 10 minutes of milling. Strong aggregation was observed for HMX milled in the absence of the stabilization mechanism. The stabilization techniques discussed in this study appeared to lead to a shorter processing time and a more efficient milling process when utilized. Under comparable milling conditions, a particle size of 180 nm could be achieved with stabilization compared to 500 nm without. Such a dramatic improvement of the milling process bodes well for future nanoHMX production, as well as that of similar materials.
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