Dissolution kinetics of sub-millimeter Composition B detonation residues: role of particle size and particle wetting

The dissolution of the 2,4,6-trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) from microscale particles (<250 μm) of the explosive formulation Composition B was examined and compared to dissolution from macroscopic particles (>0.5 mm). The dissolution of explosives from detonation soot was also examined. The measured mass transfer coefficients for the microscale particles were one to two orders of magnitude greater than the macroscopic particles. When normalized to particle surface area, mass transfer coefficients of microscale and macroscale particles were similar, indicating that the bulk dissolution processes were similar throughout the examined size range. However, an inverse relationship was observed between the particle diameter and the RDX:TNT mass transfer rate coefficient ratio for dry-attritted particles, which suggests that RDX may be more readily dissolved (relative to TNT) in microscale particles compared to macroscale particles. Aqueous weathering of larger Composition B residues generated particles that possessed mass transfer coefficients that were on the order of 5- to 20-fold higher than dry-attritted particles of all sizes, even when normalized to particle surface area. These aqueous weathered particles also possessed a fourfold lower absolute zeta-potential than dry-attritted particles, which is indicative that they were less hydrophobic (and hence, more wettable) than dry-attritted particles. The increased wettability of these particles provides a plausible explanation for the observed enhanced dissolution. The wetting history and the processes by which particles are produced (e.g., dry physical attrition vs. aqueous weathering) of Composition B residues should be considered when calculating mass transfer rates for fate and transport modeling.     

Temporal‐spatial variations of air pollutants in Lanzhou,Gansu Province,China, during the spring–summer periods, 2014–2016

In this article, we analyzed the mass concentrations of particulate matter 2.5 micrometers (µm) or less in size (PM_2.5), particulate matter 10 µm or less in size (PM₁₀), sulfur dioxide (SO₂), nitrogen dioxide (NO₂), carbon monoxide (CO), and ozone (O₃) in Lanzhou, the capital of Gansu province, China. We analyzed monitoring data collected from five air quality monitoring stations during the spring–summer period from 2014 to 2016. Our comparison of contaminant concentrations and average diurnal, daily, monthly, and annual concentrations revealed that the average concentrations of PM_2.5 and PM₁₀ amounted to 128.57 and 46.4 micrograms per cubic meters (µg/m³), respectively, exceeding the Chinese National Ambient Air Quality Standard (NAAQS). We used the Pearson correlation coefficient to establish connections between particulate matter and gaseous pollutants. The results show significant differences in the concentration levels of airborne pollutants. The Pearson correlation coefficient between PM_2.5 and PM₁₀ had the highest coefficient of r = 0.842. A correlation between the two particulate matter sizes (PM_2.5 and PM₁₀) and SO₂ was PM_2.5 and SO₂ r = 0.313; PM₁₀ and SO₂ r = 0.279; and CO and the two particulate matter sizes, PM_2.5 and CO r = 0.304; and PM₁₀ and CO r = 0.203. The average monthly ratio for the study months of PM_2.5 to PM₁₀ was 0.361. In addition, we used the hybrid single particle Lagrangian integrated trajectory model for tracking sources and pathways of the air pollutants in Lanzhou.