Effective in situ remediation of groundwater requires the successful delivery of reactive iron particles through soil. In this paper we report the transport characteristics of nanoscale zerovalent iron entrapped in porous silica particles and prepared through an aerosol-assisted process. The entrapment of iron nanoparticles into the silica matrix prevents their aggregation while maintaining the particles' reactivity. Furthermore, the silica particles are functionalized with alkyl groups and are extremely efficient in adsorbing dissolved trichloroethylene (TCE). Because of synthesis through the aerosol route, the particles are of the optimal size range (0.1-1 microm) for mobility through sediments. Column and capillary transport experiments confirm that the particles move far more effectivelythrough model soils than commercially available uncoated nanoscale reactive iron particles. Microcapillary experiments indicate that the particles partition to the interface of TCE droplets, further enhancing their potential for dense non-aqueous-phase liquid source-zone remediation.

Spherical silica particles containing nanoscale zerovalent iron were synthesized through an aerosol-assisted process. These particles are effective for groundwater remediation, with the environmentally benign silica particles serving as effective carriers for nanoiron transport. Incorporation of iron into porous sub-micrometer silica particles protects ferromagnetic iron nanoparticles from aggregation and may increase their subsurface mobility. Additionally, the presence of surface silanol groups on silica particles allows control of surface properties via silanol modification using organic functional groups. Aerosolized silica particles with functional alkyl moieties, such as ethyl groups on the surface, clearly adsorb solubilized trichloroethylene (TCE) in water. These materials may therefore act as adsorbents which have coupled reactivity characteristics. The nanoscale iron/silica composite particles with controlled surface properties have the potential to be efficiently applied for in situ source depletion and in the design of permeable reactive barriers.

Spherical iron-carbon nanocomposites were developed through a facile aerosol-based process with sucrose and iron chloride as starting materials. These composites exhibit multiple functionalities relevant to the in situ remediation of chlorinated hydrocarbons such as trichloroethylene (TCE). The distribution and immobilization of iron nanoparticles on the surface of carbon spheres prevents zerovalent nanoiron aggregation with maintenance of reactivity. The aerosol-based carbon microspheres allow adsorption of TCE, thus removing dissolved TCE rapidly and facilitating reaction by increasing the local concentration of TCE in the vicinity of iron nanoparticles. The strongly adsorptive property of the composites may also prevent release of any toxic chlorinated intermediate products. The composite particles are in the optimal range for transport through groundwater saturated sediments. Furthermore, those iron-carbon composites can be designed at low cost, the process is amenable to scale-up for in situ application, and the materials are intrinsically benign to the environment.

Nanoscale zerovalent iron particles (NZVI) are a preferred option for reductive dehalogenation of dense nonaqueous phase chlorinated hydrocarbons such as trichloroethylene (TCE) because of their environmentally benign nature, high efficiency, and low cost. This study describes an approach to engineered particles containing NZVI that are effective targeted delivery agents for the remediation of these compounds. The particles contain highly uniform carbon microspheres embedded with NZVI (Fe0/C composite particles). The highly adsorptive carbon keeps the TCE in the proximity of the reactive sites and serves as a sorptive sink for TCE removal. The Fe0/C composite particles are in the optimal size range for transport through soil and the polyelectrolyte (Carboxymethyl cellulose, CMC) is used to stabilize the composite microspheres in aqueous solution. The multiple functionalities associated with these particles can be designed at low cost and the materials are environmentally benign.

Effective in situ injection technology for the remediation of dense nonaqueous phase liquids (DNAPLs) such as trichloroethylene (TCE) requires the use of decontamination agents that effectively migrate through the soil media and react efficiently with dissolved TCE and bulk TCE. We describe the use of a novel decontamination system containing highly uniform carbon microspheres in the optimal size range for transport through the soil. The microspheres are enveloped in a polyelectrolyte (carboxymethyl cellulose, CMC) to which a bimetallic nanoparticle system of zero-valent iron and Pd is attached. The carbon serves as a strong adsorbent to TCE, while the bimetallic nanoparticle system provides the reactive component. The polyelectrolyte serves to stabilize the carbon microspheres in aqueous solution. The overall system resembles a colloidal micelle with a hydrophilic shell (polyelectrolyte coating) and hard hydrophobic core (carbon). In contact with bulk TCE, there is a sharp partitioning of the system to the TCE side of the interface due to the hydrophobicity of the core. These multifunctional systems appear to satisfy criteria related to remediation and are made with potentially environmentally benign materials.