Shaw Environmental, Inc., 17 Princess Road, Lawrenceville, NJ 08648, USA.
Chemosphere. 2012 Jul;88(5):591-7. doi: 10.1016/j.chemosphere.2012.03.038. Epub 2012 Apr 6.
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 (<250μm) of the explosive formulation Composition B was examined and compared to dissolution from macroscopic particles (>0.5mm). 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.
从爆炸物配方 B 的微尺度颗粒(<250μm)中检查并比较了 2,4,6-三硝基甲苯(TNT)、六氢-1,3,5-三硝基-1,3,5-三嗪(RDX)和八氢-1,3,5,7-四硝基-1,3,5,7-四唑(HMX)的溶解情况,以及爆炸物从爆震烟尘中的溶解情况。测量的微尺度颗粒的传质系数比宏观颗粒大一到两个数量级。当归一化到颗粒表面积时,微尺度和宏观颗粒的传质系数相似,表明在整个考察的尺寸范围内,体相溶解过程相似。然而,对于干磨蚀颗粒,观察到粒径与 RDX:TNT 传质速率系数比之间存在反比关系,这表明与宏观颗粒相比,RDX 在微尺度颗粒中可能更容易溶解(相对于 TNT)。较大的 B 型炸药残留物的水相风化生成的颗粒具有的传质系数比所有尺寸的干磨蚀颗粒高 5-20 倍,即使归一化到颗粒表面积也是如此。这些水相风化的颗粒的绝对zeta 电位也比干磨蚀颗粒低四倍,这表明它们的疏水性(因此,润湿性)比干磨蚀颗粒低。这些颗粒的高润湿性为观察到的增强溶解提供了一个合理的解释。在计算命运和传输建模的传质速率时,应考虑 B 型炸药残留物的润湿历史和颗粒生成的过程(例如,干物理磨损与水相风化)。