Thermal Breakdown Mechanisms of Emulsion Explosives in Deep Mining
High Resolution Image Download MS PowerPoint Slide The longevity of emulsion explosives under extreme thermal conditions (up to 150 °C) is dictated by specific molecular-level degradation pathways, where surfactant headgroup reactivity, salt type, and chemical stabilizers determine interfacial integrity. Thermal breakdown mechanisms of emulsion explosives were investigated at temperatures up to 150 °C, analyzing the effects of surfactant chemistry and additives on rheological performance and interfacial stability. We demonstrate that at 150 °C, the heat-induced hydrolysis of ester headgroup emulsifiers severely degrades the interfacial surfactant film, causing interfacial film rupture, significant coalescence (∼50 μm drops), and subsequent crystallization. While heating breaks urea-containing emulsions through ammonia-induced interfacial weakening (increased G′), stability is tunable: sodium ions enhance thermal stability via strong Na + -PIBSA binding, whereas calcium ions induce rapid crystallization in the presence of urea. These findings establish the key degradation pathways to improve the high-temperature stability of explosive formulations.
Authors
- Brian S. Hawkett (ORCID: https://orcid.org/0000-0001-7609-0127)
- Gregory G. Warr (ORCID: https://orcid.org/0000-0002-6893-1253)
- Pramith Priyananda (ORCID: https://orcid.org/0000-0003-1189-3097)
- Nathan Paris
- Alexander M Djerdjev (ORCID: https://orcid.org/0000-0001-6143-2497)
Institutions
- The University of Sydney (AU)
Publication Details
- Journal
- ACS Omega
- Published
- 2026-06-29
- DOI
- https://doi.org/10.1021/acsomega.6c01794
- Primary Topic
- Energetic Materials and Combustion
- Type
- article
- Field-Weighted Citation Impact
- 0.00