A supercritical antisolvent (SAS) process was used to prepare micronized cyclotrimethylenetrinitramin (RDX). This study examined the influence of different solvents at a fixed temperature (50 °C) and pressure (13.7 or 15 MPa) on the morphology, particle size (PS), and particle size distribution (PSD) using a semicontinuous SAS process. Dimethyl sulfoxide (DMSO), dimethylformamide (DMF), acetone (AC), acetonitrile (ACN), n-methyl 2-pyrrolidone (NMP), and cyclohexanone (CHN) were used as solvents. The recrystallized RDX particles were characterized by scanning electron microscopy (SEM), particle size analyzer (PSA), Fourier transform infrared (FT-IR) spectroscopy, and differential scanning calorimetry (DSC). Depending on the solvent used, the recrystallized RDX particles showed a variety of morphologies, particle sizes, and particle size distributions (PSD). The mean particle size of the recrystallized RDX ranged from 2.6 to 17.7 µm. The enthalpy change (∆H ) 583.4, 847.7, 967.1, 823.9, 1131, and 1620 J/g) for the exothermic decomposition of recrystallized RDX was much higher than that of the unprocessed RDX (∆H ) 381.5 J/g).
Dense phase carbon dioxide (DPCD) is one of the most promising techniques available to control microorganisms as a non-thermal disinfection method. However, no study on the efficiency of biofilm disinfection using DPCD has been reported. The efficiency of DPCD in inactivating Pseudomonas aeruginosa biofilm, which is known to have high antimicrobial resistance, was thus investigated. P. aeruginosa biofilm, which was not immersed in water but was completely wet, was found to be more effectively inactivated by DPCD treatment, achieving a 6-log reduction within 7 min. The inactivation efficiency increased modestly with increasing pressure and temperature. This study also reports that the water-unimmersed condition is one of the most important operating parameters in achieving efficient biofilm control by DPCD treatment. In addition, observations by confocal laser scanning microscopy revealed that DPCD treatment not only inactivated biofilm cells on the glass coupons but also caused detachment of the biofilm following weakening of its structure as a result of the DPCD treatment; this is an added benefit of DPCD treatment.
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