Dynamics of lead immobilization in sulfate reducing biofilms

We have evaluated the effects of selected minerals present in subsoil environment on the efficiency of lead removal from contaminated groundwaters using biofilms composed of sulfate-reducing microorganisms, and examined the stability of metal deposits after the biofilms had been temporarily exposed to the air. To quantify the studied effects, lead was immobilized in biofilms of Desulfovibrio desulfuricans grown anaerobically in two flat-plate flow reactors, one filled with hematite and the other with quartz. While the biofilms in both reactors were heterogeneous and consisted of voids and channels, the biofilms grown on hematite were denser, thicker, and more porous than those grown on quartz. The average H₂S concentrations, measured using microelectrodes, were higher in the biofilms grown on quartz than those measured in the biofilms grown on hematite. During 18 weeks of operation, iron was continuously released from the hematite. Lead was immobilized more efficiently in the biofilms grown on quartz than it was in the biofilms grown on hematite. Lead deposits were partially reoxidized, especially in biofilms grown on hematite, and the biofilms in both reactors responded to the presence of oxygen by lowering their density and increasing the H₂S production rate.     

Equilibrium and kinetics studies for adsorption of direct blue 71 from aqueous solution by wheat shells

This paper deals with the application of wheat shells (WS), an agricultural by-product, for the removal of direct blue 71 (DR) from aqueous solution. The characteristics of WS surface, such as surface area, Bohem titration and scanning electron microscopy (SEM) were obtained. The removal of direct blue 71 onto WS from aqueous solution was investigated by using parameters, such as pH, temperature, adsorbent dose, contact time and initial concentration. The adsorption process attains equilibrium within 36 h. The extent of dye removal decreased with increasing adsorbent dosage and also increased with increasing contact time, temperature, in solution concentration. Optimum pH value for dye adsorption was determined between 6 and 8. The experimental data were analysed by the Langmuir and Freundlich models of adsorption. It was found that the Langmuir equation fit better than the Freundlich equation. Maximum adsorption capacity (Q(m)) was calculated as at different temperatures (293, 303 and 313 K) 40.82, 45.66 and 46.30 mgg(-1), respectively. In addition, the adsorption data obtained at different temperatures of DR by WS were applied to pseudo first-order, pseudo second-order and Weber-Morris equations, and the rate constants of first-order adsorption (k(1)), the rate constants of second-order adsorption (k(2)) and intraparticle diffusion rate constants (k(3)) at these temperatures were calculated, respectively. The rates of adsorption were found to conform to pseudo second-order kinetics with good correlation (R(2)>or=0.9904). Also, free energy of adsorption (DeltaG degrees), enthalpy (DeltaH degrees), and entropy (DeltaS degrees) changes were determined to predict the nature of adsorption. Furthermore, the results indicate that WS could be employed as a low-cost alternative to other adsorbents in the removal of direct blue 71 from aqueous solution.     

Preparation and properties of polybenzidine film-coated electrode as an H2O2 selective polymeric material

By means of electrochemical polymerization, polybenzidine-modified electrodes were prepared in an aqueous monomer solution at a potential of 0.7 V versus Ag/AgCl. The permselective character of the polybenzidine electrode prepared in a one-step procedure was examined for electroactive (ascorbic acid, oxalic acid, and hydrogen peroxide) and nonelectroactive (lactose, sucrose, and urea) species. Influence of the various parameters on the permselective properties of the polybenzidine membrane was systematically investigated and the optimal values for these parameters were determined. It has been found that polybenzidine membrane showed selective permeation for hydrogen peroxide while blocking the permeation of electroactive and nonelectroactive interferents through film. In brief, it is claimed that this polybenzidine film can be used as a coating material to prevent interferences in electrochemical biosensor applications. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 70: 2227–2234, 1998     

Thread vulnerability in parallel applications

Continuously reducing transistor sizes and aggressive low power operating modes employed by modern architectures tend to increase transient error rates. Concurrently, multicore machines are dominating the architectural spectrum today in various application domains. These two trends require a fresh look at resiliency of multithreaded applications against transient errors from a software perspective. In this paper, we propose and evaluate a new metric called the Thread Vulnerability Factor (TVF$TVF$). A distinguishing characteristic of TVF$TVF$ is that its calculation for a given thread (which is typically one of the threads of a multithreaded application) does not depend on its code alone, but also on the codes of the threads that share resources and data with that thread. As a result, we decompose TVF$TVF$ of a thread into two complementary parts: local and remote. While the former captures the TVF$TVF$ induced by the code of the target thread, the latter represents the vulnerability impact of the threads that interact with the target thread. We quantify the local and remote TVF$TVF$ values for three architectural components (register file, ALUs, and caches) using a set of ten multithreaded applications from the Parsec and Splash-2 benchmark suites. Our experimental evaluation shows that TVF$TVF$ values tend to increase as the number of cores increases, which means the system becomes more vulnerable as the core count rises. We further discuss how TVF$TVF$ metric can be employed to explore performance–reliability tradeoffs in multicores. Reliability-based analysis of compiler optimizations and redundancy-based fault tolerance are also mentioned as potential usages of our TVF$TVF$ metric.     

High-Temperature Oxidation of Boron Nitride: I, Monolithic Boron Nitride

High-temperature oxidation of monolithic boron nitride (BN) is examined at 900–1200°C. Hot-pressed BN and both low- and high-density chemically vapor-deposited BN are studied. The oxidation product is B₂O₃( l ) and the oxidation kinetics are sensitive to crystallographic orientation, porosity, and impurity levels. The B₂O₃ product also reacts readily with ambient water vapor in the test furnace (ppm levels) to form the volatile species HBO₂( g ), leading to overall paralinear kinetics. The linear rate constant extracted from these experiments agreed with that predicted from diffusion of HBO₂( g ) across a static boundary layer.     

Microscale geochemical gradients in Hanford 300 Area sediment biofilms and influence of uranium

The presence and importance of microenvironments in the subsurface at contaminated sites were suggested by previous geochemical studies. However, no direct quantitative characterization of the geochemical microenvironments had been reported. We quantitatively characterized microscale geochemical gradients (dissolved oxygen (DO), H₂, pH, and redox potential) in Hanford 300A subsurface sediment biofilms. Our results revealed significant differences in geochemical parameters across the sediment biofilm/water interface in the presence and absence of U(VI) under oxic and anoxic conditions. While the pH was relatively constant within the sediment biofilm, the redox potential and the DO and H₂ concentrations were heterogeneous at the microscale (<500-1000 μm). We found microenvironments with high DO levels (DO hotspots) when the sediment biofilm was exposed to U(VI). On the other hand, we found hotspots (high concentrations) of H₂ under anoxic conditions both in the presence and in the absence of U(VI). The presence of anoxic microenvironments inside the sediment biofilms suggests that U(VI) reduction proceeds under bulk oxic conditions. To test this, we operated our biofilm reactor under air-saturated conditions in the presence of U(VI) and characterized U speciation in the sediment biofilm. U L_III-edge X-ray absorption spectroscopy (XANES and EXAFS) showed that 80-85% of the U was in the U(IV) valence state.     

Spectrophotometric and electrochemical behavior of a novel azocalix[4]arene derivative as a highly selective chromogenic chemosensor for Cr

In this study, a novel azocalix[4]arene derivative, 5,11,17-tris[(1-naphtyl)azo]-25,26,27,28-tetrahydroxy-calix[4]arene (NAC4) bearing napthyl groups on the upper rim was synthesized. Its complexation behavior for alkali, alkaline-earth and various heavy metal ions (Li⁺, Na⁺, K⁺, Rb⁺, Cs⁺, Mg²⁺, Ca²⁺, Sr²⁺, Ba²⁺, Pb²⁺, Hg²⁺, Ni²⁺, Cd²⁺, Cu²⁺, Zn²⁺, Co²⁺, Fe²⁺, Cr³⁺, Ag⁺) was investigated by spectroscopic and voltammetric methods. This chemosensor exhibits decreased absorbance in the presence of Hg²⁺ and a unique absorbance quenching effect only for Cr³⁺. In addition, a new absorption band centered at 565 nm with the formation of the 1:1 host–guest complex (Cr³⁺-NAC4) was observed in the case of Cr³⁺, leading to an obvious color change from light orange to dark lilac. In voltammetric experiments, Cr³⁺ ions decreased voltammetric peaks of NAC4, whereas no significant changes occurred in the presence of the other metal ions. The Benesi–Hildebrand method was used to determine a logarithmic value of 3.76 for the association constant of the complex between Cr³⁺ and NAC4.     

Power management system for a 2.5 W remote sensor powered by a sediment microbial fuel cell

One of the challenges in using wireless sensors that require high power to monitor the environment is finding a renewable power source that can produce enough power. Sediment microbial fuel cells (SMFCs) are considered an alternative renewable power source for remote monitoring, but current research on SMFCs has demonstrated that they can only produce several to tens of mW of continuous power. This limits the use of SMFCs as an alternative renewable remote power source to mW-level power. Such low power is only enough to operate a low-power sensors. However, there are many remote sensors that require higher power, on the order of watts. Current technology using a SMFC to power a remote sensor requiring watts-level intermittent power is limited because of limitations of power management technology. Our goal was to develop a power management system (PMS) that enables a SMFC to operate a remote sensor consuming 2.5 W of power. We designed a custom PMS to store microbial energy in capacitors and use the stored energy in short bursts. Our results demonstrate that SMFCs can be a viable alternative renewable power source for remote sensors requiring high power.     

The Nucleation Effect of PbSe Additive on Bi2Sr2CaCu2Oδ Glass Ceramics

Glass and Ceramics - The crystallisation kinetics and effects of doping on Bi2Sr2CaCu2Oδ (BSCCO) glass ceramic system with 0.0%, 0.1%, 0.3% and 0.5% PbSe were investigated in this study....