RESUMEN
This research investigates the use of polymeric matrices to encapsulate solid sorbents used to remove arsenic from drinking water. Arsenic-containing granular ferric oxy/hydroxide and ferric hydroxide amended alumina residuals were encapsulated in a polymeric matrix using a novel aqueous-based manufacturing process. The polymer was a blend of poly(styrene butadiene) and an epoxy resin. The polymeric waste forms produced were capable of containing more than 60 wt% of sorbent (dry basis), while keeping good mechanical properties. Arsenic leaching from encapsulated and unencapsulated residuals was evaluated using the standard toxicity characteristic leaching procedure (TCLP) and the California Waste Extraction Test (CA-WET). The results show that waste forms of the polymer-encapsulated residuals crushed for testing retain good leaching resistance when evaluated with the more aggressive CA-WET test, yielding leachate arsenic concentrations below the toxicity characteristic (TC) standard of 5mg/L. When residuals were preprocessed and encapsulated in a polymer form that avoided the size reduction required by leaching protocols, arsenic leached up to 700 times less than that from the unencapsulated residuals. Comparison of the waste form developed here with conventional cement matrices containing the same residuals show that the polymeric matrices were capable of encapsulating appreciably more material and leached arsenic at concentration levels that were more than an order of magnitude lower than cement.
Asunto(s)
Arsénico/química , Polímeros/química , Microscopía Electrónica de RastreoRESUMEN
The dynamics of disassembly of microtubules deposited on surfaces is shown to be strongly dependent on the electrostatic interaction between the microtubule and the substrate. Fluorescence microscopy of microtubules adsorbed on a Poly-L-Lysine film and immersed in pure water show a drastic decrease in disassembly velocity compared to the microtubules in bulk water solutions. While microtubules suspended in pure water disassemble in seconds, the dissociation velocity of microtubules adsorbed on a Poly-L-Lysine film ranges from 0.8 to 1.0 microm/min in pure water. Kinetic Monte Carlo simulations of the microtubule dynamics indicate that a decrease in the dissociation velocity of unstable microtubules can be achieved by reducing the heterodimer dissociation rate constant of tubulin heterodimers constituting a single protofilament, adsorbed to the Poly-L-Lysine film. This model suggests that the reduction of the dissociation velocity originates from the electrostatic interactions between the positively charged amino groups of the Poly-L-Lysine film and the negatively charged microtubule surface.
Asunto(s)
Microtúbulos/química , Adsorción , Simulación por Computador , Nanotecnología , Propiedades de SuperficieRESUMEN
We demonstrate the fabrication of a unique optical device, the single leakage-channel grating coupler, using solgel techniques. Design specifications are outlined to establish the material criteria for the sol-gel compositions. Material choice and preparation are described. We evaluate the characteristics and performance of the single leakage-channel grating coupler by comparing the predicted and the measured branching ratios. The branching ratio of the solution-derived device is within 3% of the theoretically predicted value.
RESUMEN
We describe the modeling and fabrication of waveguide grating couplers with theoretical outcoupling efficiencies into a single diffracted order nearing 100%. Termed single leakage-channel grating couplers (or SLCGC's), these devices utilize a high-reflectivity dielectric stack to reflect the outcoupled beam diffracted toward the substrate and back up into the air region, where it constructively adds with the beam diffracted into the air region. Computer modeling shows that the branching ratio and the leakage rate can be independently controlled, and that the branching ratio is independent of grating depth and grating period. A SLCGC with a branching ratio of 97.1% is fabricated by the use of a combination of vacuum-evaporation and wet-chemical techniques.