Zero valent iron (Fe 0) nanoparticles (NZVI) have been used for groundwater remediation of various contaminants because of their unique physiochemical properties. Various chlorinated aliphatic hydrocarbons, explosive material, and arsenic have been successfully decontaminated by NZVI. However, NZVI are not only highly reactive with the contaminants, but also rapidly react with surrounding media in the subsurface (dissolved oxygen and/or water) and other non-target compounds. Thus, significant loss of NZVI reactivity occurs before the particles reach the target contaminant. Additionally, strong magnetic interaction between particles causes agglomeration, limiting colloidal stability and reduction in reactive surface. Considering the requirements of an effective delivery system for NZVI, functionalized amphiphilic polysiloxanes are an ideal class of polymers for this application. Amphiphilic polysiloxane graft copolymers (APGCs) have been synthesized by hydrosilylation of hydride-functional polysiloxanes, poly ethylene glycol (PEG) and tert-butyl acrylate (tBA). Anchoring groups and carboxylic acid groups, in conjunction with the polysiloxane polymer backbone, will allow for efficient absorption of polymer molecules to the surface of the NZVI while the water-soluble grafts, PEG, will allow for dispersibility and colloidal stability in an aqueous medium. The hydrophobicity of the polysiloxane polymer backbone will protect the NZVI from excessive oxidation by water/non-target compounds by creating a barrier while also creating an affinity of the coated NZVI for the water/contaminant interface. Since polysiloxanes are very hydrophobic they will have a high affinity for the water/contaminant interface. They will also readily allow permeation of contaminants to the NZVI surface.

Project Objectives :

1. Synthesize and characterize the NZVI through transmission electron microscopy (TEM), scanning electron microscopy with X-ray microanalysis (SEM/EDS), X-ray diffraction (XRD), and BET surface area analysis.
2. Synthesize the APGCs by hydrosilylation and characterize using nuclear magnetic resonance spectroscopy (NMR) and Fourier transform infrared spectroscopy (FTIR).
3. Study colloidal stability of APGCs coated NZVI and compare with uncoated NZVI.
4. Compare the degree of oxidation by non-target compounds of APGCs coated and bare NZVI.
5. Study degradation kinetics of TCE and As(III) by APGCs coated NZVI and compare with kinetics data obtained with bare NZVI.