Saebom Ko

Control of manganese dioxide particles resulting from in situ chemical oxidation using permanganate.

In situ chemical oxidation using permanganate is an approach to organic contaminant site remediation. Manganese dioxide particles are products of permanganate reactions. These particles have the potential to deposit in the subsurface and impact the flow-regime in/around permanganate injection, including the well screen, filter pack, and the surrounding subsurface formation. Control of these particles can allow for improved oxidant injection and transport and contact between the oxidant and contaminants of concern. The goals of this research were to determine if MnO(2) can be stabilized/controlled in an aqueous phase, and to determine the dependence of particle stabilization on groundwater characteristics. Bench-scale experiments were conducted to study the ability of four stabilization aids (sodium hexametaphosphate (HMP), Dowfax 8390, xanthan gum, and gum arabic) in maintaining particles suspended in solution under varied reaction conditions and time. Variations included particle and stabilization aid concentrations, ionic content, and pH. HMP demonstrated the most promising results, as compared to xanthan gum, gum arabic, and Dowfax 8390 based on results of spectrophotometric studies of particle behavior, particle filtration, and optical measurements of particle size and zeta potential. HMP inhibited particle settling, provided for greater particle stability, and resulted in particles of a smaller average size over the range of experimental conditions evaluated compared to results for systems that did not include HMP. Additionally, HMP did not react unfavorably with permanganate. These results indicate that the inclusion of HMP in a permanganate oxidation system improves conditions that may facilitate particle transport.

Enhanced permanganate in situ chemical oxidation through MnO2 particle stabilization: Evaluation in 1-D transport systems

In situ chemical oxidation using permanganate is an increasingly employed approach to organic contaminant remediation at hazardous waste sites. Manganese dioxide (MnO2) particles form as a by-product of the reaction of permanganate with contaminants and naturally-reduced subsurface materials. These particles are of interest because they have the potential to deposit in the subsurface and impact the flow regime in/around permanganate injection, including the well screen, filter pack, and the surrounding subsurface formation. Control of these particles can allow for improved oxidant injection and transport, and contact between the oxidant and contaminants of concern. Sodium hexametaphosphate (HMP) has previously been identified as a promising aid to stabilize MnO2 in solution when included in the oxidizing solution, increasing the potential to inhibit particle deposition and impact subsurface flow. The goal of the experimental studies described herein was to investigate the ability of HMP to prevent particle deposition in transport studies using four different types of porous media. Permanganate was delivered to a contaminant source zone (trichloroethylene) located within four different media types with variations in sand, clay, organic carbon, and iron oxides (as goethite) content. Deposition of MnO2 within the columns was quantified with distance from the source zone. Experiments were repeated in replicate columns with the inclusion of HMP directly with the oxidant delivery solution, and MnO2 deposition was again quantified. While total MnO2 deposition within the 60 cm columns did not change significantly with the addition of HMP, deposition within the contaminant source zone decreased by 25-85%, depending on the specific media type. The greatest differences in deposition were observed in the goethite-containing and clay-containing columns. Columns containing these two media types experienced completely plugged flow in the oxidant-only delivery systems; however, the addition of HMP prevented this plugging within the columns, increasing the oxidant throughput.

Measuring and modeling the magnetic settling of superparamagnetic nanoparticle dispersions.

In this paper, we present settling experiments and mathematical modeling to study the magnetic separation of superparamagnetic iron-oxide nanoparticles (SPIONs) from a brine. The experiments were performed using SPIONs suspensions of concentration between 3 and 202g/L dispersed in water and separated from the liquid under the effect of a permanent magnet. A 1D model was developed in the framework of the sedimentation theory with a conservation law for SPIONs and a mass flux function based on the Newtons law for motion in a magnetic field. The model describes both the hindering effect of suspension concentration (n) during settling due to particle collisions and the increase in settling rate due to the attraction of the SPIONs towards the magnet. The flux function was derived from the settling experiments and the numerical model validated against the analytical solution and the experimental data. Suspensions of SPIONs were of 2.8cm initial height, placed on a magnet, and monitored continuously with a digital camera. Applying a magnetic field of 0.5T of polarization, the SPIONs velocity was of approximately 3·10(-5)m/s close to the magnet and decreases of two orders of magnitude across the domain. The process was characterized initially by a classical sedimentation behavior, i.e., an upper interface between the clear water and the suspension slowly moving towards the magnet and a lower interface between the sediment layer and the suspension moving away from the magnet. Subsequently, a rapid separation of nanoparticle occured suggesting a non-classical settling phenomenon induced by magnetic forces which favor particle aggregation and therefore faster settling. The rate of settling decreased with n and an optimal condition for fast separation was found for an initial n of 120g/L. The model agrees well with the measurements in the early stage of the settling, but it fails to describe the upper interface movement during the later stage, probably because of particle aggregation induced by magnetization which is not accounted for in the model.

Highly porous CO2 hydrate generation aided by silica nanoparticles for potential secure storage of CO2 and desalination

We report a new way of storing CO2 in a highly porous hydrate structure, stabilized by silica nanoparticles (NPs). Such a porous CO2 hydrate structure was generated either by cooling down NP-stabilized CO2-in-seawater foams, or by gently mixing CO2 and seawater that contains silica NPs under CO2 hydrate-generating conditions. With the highly porous structure, enhanced desalination was also achievable when the partial meltdown of CO2 hydrate was allowed.

Recent Advances Incorporating Superparamagnetic Nanoparticles into Immunoassays

Superparamagnetic nanoparticles (SPMNPs) have attracted interest for various biomedical applications due to their unique magnetic behavior, excellent biocompatibility, easy surface modification, and low cost. Their unique magnetic properties, superparamagnetism, and magnetophoretic mobility have led to their inclusion in immunoassays to enhance biosensor sensitivity and allow for rapid detection of various analytes. In this review, we describe SPMNP characteristics valuable for incorporation into biosensors, including the use of SPMNPs to increase detection capabilities of surface plasmon resonance and giant magneto-resistive biosensors. The current status of SPMNP-based immunoassays to improve the sensitivity of rapid diagnostic tests is reviewed, and suggested strategies for the successful adoption of SPMNPs for immunoassays are presented.

Field demonstration of polymer-amended in situ chemical oxidation (PA-ISCO)

The methods and results of the first field-scale demonstration of polymer-amended in situ chemical oxidation (PA-ISCO) are presented. The demonstration took place at MCB CAMLEJ (Marine Corps Base, Camp Lejeune) Operable Unit (OU) 15, Site 88, in Camp Lejeune, North Carolina between October and December 2010. PA-ISCO was developed as an alternative treatment approach that utilizes viscosity-modified fluids to improve the in situ delivery and distribution (i.e. sweep-efficiency) of chemical oxidants within texturally heterogeneous contaminated aquifers. The enhanced viscosity of the fluid mitigates the effects of preferential flows, improving sweep-efficiency and enhancing the subsurface contact between the injected oxidant and the target contamination within the treatment zone. The PA-ISCO fluid formulation used in this demonstration included sodium permanganate as oxidant, xanthan gum biopolymer as a shear-thinning viscosifier, and sodium hexametaphosphate (SHMP) as an anti-coagulant. It was the goal of this demonstration to validate the utility of PA-ISCO within a heterogeneous aquifer. An approximate 100% improvement in sweep-efficiency was achieved for the PA-ISCO fluid, as compared to a permanganate-only injection within an adjacent control plot.