Environmental Effects on Zirconium Hydroxide Nanoparticles and Chemical Warfare Agent Decomposition: Implications of Atmospheric Water and Carbon Dioxide.

Abstract

Zirconium hydroxide (Zr(OH)4) has excellent sorption properties and wide-ranging reactivity toward numerous types of chemical warfare agents (CWAs) and toxic industrial chemicals. Under pristine laboratory conditions, the effectiveness of Zr(OH)4 has been attributed to a combination of diverse surface hydroxyl species and defects; however, atmospheric components (e.g., CO2, H2O, etc.) and trace contaminants can form adsorbates with potentially detrimental impact to the chemical reactivity of Zr(OH)4. Here, we report the hydrolysis of a CWA simulant, dimethyl methylphosphonate (DMMP) on Zr(OH)4 determined by gas chromatography-mass spectrometry and in situ attenuated total reflectance Fourier transform infrared spectroscopy under ambient conditions. DMMP dosing on Zr(OH)4 formed methyl methylphosphonate and methoxy degradation products on free bridging and terminal hydroxyl sites of Zr(OH)4 under all evaluated environmental conditions. CO2 dosing on Zr(OH)4 formed adsorbed (bi)carbonates and interfacial carbonate complexes with relative stability dependent on CO2 and H2O partial pressures. High concentrations of CO2 reduced DMMP decomposition kinetics by occupying Zr(OH)4 active sites with carbonaceous adsorbates. Elevated humidity promoted hydrolysis of adsorbed DMMP on Zr(OH)4 to produce methanol and regenerated free hydroxyl species. Hydrolysis of DMMP by Zr(OH)4 occurred under all conditions evaluated, demonstrating promise for chemical decontamination under diverse, real-world conditions.