Sublimation and Diffusion Kinetics of 2,4,6-Trinitrotoluene (TNT) Single Crystals by Atomic Force Microscopy (AFM).

In this article, we report the in-situ nanoscale experimental measurement of sublimation rates, activation energy of sublimation, and diffusion coefficients of 2,4,6-trinitrotoluene (TNT) single crystals in air using atomic force microscopy (AFM). The crystals were prepared by slow evaporation at 5 °C using acetone-dissolved TNT. The mass loss was calculated by monitoring the shrinkage of the surface area of layered islands formed on the surface of the TNT crystals due to sublimation upon isothermal heating at temperatures below the melting point.

Non-Isothermal Sublimation Kinetics of 2,4,6-Trinitrotoluene (TNT) Nanofilms.

Non-isothermal sublimation kinetics of low-volatile materials is more favorable over isothermal data when time is a crucial factor to be considered, especially in the subject of detecting explosives. In this article, we report on the in-situ measurements of the sublimation activation energy for 2,4,6-trinitrotoluene (TNT) continuous nanofilms in air using rising-temperature UV-Vis absorbance spectroscopy at different heating rates. The TNT films were prepared by the spin coating deposition technique.

Sublimation kinetics and diffusion coefficients of TNT, PETN, and RDX in air by thermogravimetry.

The diffusion coefficients of explosives are crucial in their trace detection and lifetime estimation. We report on the experimental values of diffusion coefficients of three of the most important explosives in both military and industry: TNT, PETN, and RDX. Thermogravimetric analysis (TGA) was used to determine the sublimation rates of TNT, PETN, and RDX powders in the form of cylindrical billets.

In situ direct measurement of vapor pressures and thermodynamic parameters of volatile organic materials in the vapor phase: benzoic acid, ferrocene, and naphthalene.

We report the direct determination of vapor pressures and optical and thermodynamic parameters of powders of low-volatile materials in their vapor phase using a commercial UV/Vis spectrometer. This methodology is based on the linear proportionality between the density of the saturated gas of the material and the absorbance of the gas at different temperatures. The vapor pressure values determined for benzoic acid and ferrocene are in good agreement with those reported in the literature with ∼2-7 % uncertainty.

Rapid estimation of thermodynamic parameters and vapor pressures of volatile materials at nanoscale.

Non-isothermal measurements of thermodynamic parameters and vapor pressures of low-volatile materials are favored when time is a crucial factor to be considered, such as in the case of detection of hazardous materials. In this article, we demonstrate that optical absorbance spectroscopy can be used non-isothermally to estimate the thermodynamic properties and vapor pressures of volatile materials with good accuracy. This is the first method to determine such parameters in nanoscale in just minutes.

Thermo-optical determination of vapor pressures of TNT and RDX nanofilms.

Accurate thermodynamic parameters of thin films of explosives are important for understanding their behavior in the nanometer scale as well as in standoff detection. Using UV-absorbance spectroscopy technique, accurate thermodynamic parameters such as activation energies of sublimation, sublimation rates, and vapor pressures of the explosives cyclotrimethylenetrinitramine (RDX) and 2,4,6-trinitrotoluene (TNT) were determined. The values of these parameters are in excellent agreement with those reported using traditional experiments based on gravimetry.

Simple method for determining the vapor pressure of materials using UV-absorbance spectroscopy.

Accurate thermodynamic parameters of thin films of materials are crucial in understanding their behavior in the nanometer scale. A new and simple method for determining the vapor pressure and thermodynamic properties of nanometer thick films of materials was developed based on UV-absorbance spectroscopy. Well-characterized benzoic acid was used to calibrate the spectrometer and the experimental conditions.

Early events in 2,4,6-trinitrotoluene (TNT) degradation by porphyrins: binding of TNT to porphyrin by hydrophobic and hydrogen bonds.

The interaction of meso-tri(4-sulfonatophenyl)mono(4-carboxyphenyl) porphyrin (C1TPP) with 2,4,6-trinitrotoluene (TNT) has been explored by UV-vis and fluorescence spectroscopy. The influence of temperature on the interaction has also been studied. C1TPP binds to TNT at pH 7.