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An enantioselective molecular sensor was fabricated by inserting a chiral ligand, N-carbobenzoxy-L-aspartic acid (N-CBZ-L-Asp) or N-CBZ-D-Asp, into an octadecylsiloxane (ODS) monolayer by polysiloxane film immobilization (PFI). The resulting system can recognize one enantiomer of aspartic acids (Asps) due to the chiral ligand exchange reaction at the N-CBZ-L-/D-Asp modified indium tin oxide (ITO)-coated electrode. The enantioselective formation of diastereoisomeric complexes of Cu(II) with target enantiomers, in here L-/D-Asps, and N-CBZ-L-/D-Asp immobilized by PFI on the ITO electrode. Those diastereoisomeric complexes have different thermodynamic stabilities and Nernst factors and thus enable the sensors to convert the enantioselective recognition event into potential changes by detecting Asp enantiomers in a concentration range of (4.0 x [10.sup.-8])-(8.9 x [10.sup.-5]) M without any pre- or postseparation process. The enantiomeric selectivity coefficients of the sensors for the counterisomers were in the range of(4.0 x [10.sup.-5])-(5.0 x [10.sup.-5]).

The air plasma effluent of an arc-seed microwave torch is used to kill bacterial spores contained inside an envelope. The torch is operated at a 60-Hz periodic mode (with about 40% duty cycle) and runs stably at a low airflow rate (e.g., 0.3931/s). The images of plasma torch plumes show that the arc loop of the discharge prolongs from the electrodes by nearly 3 cm and microwave energizes the charge particles along the arc loop considerably. The emission spectroscopy of the torch indicates that the plasma effluent contains an abundance of reactive atomic oxygen. Bacillus cereus is chosen for the biological agent in the decontamination experiment. The experiment and the decontamination efficacy of this torch are presented. The averaged temperature inside the envelope is measured to be less than 40 [degrees]C, thus ruling out the thermal decontamination mechanism. Index Terms--Biological warfare agents, decontamination, microwave plasma torch (MPT), oxidation, spores.

The occurrence of scanning electron microscopy (SEM) and atomic force microscopy (AFM) side-by-side is becoming increasingly common in analytical research. This article shows microscopy techniques to image Bacillus spores, to measure spore dimensions, and to demonstrate how these methods provide supplementary information to study plasma torch effects. This paper demonstrates that observed morphologies of spores before and after exposure to a plasma torch are remarkably different. The use of SEM and AFM as a tool complex enables examination of spore morphology and dimensions as well as their alterations during decontamination using plasma torch. Index Terms--Atomic force microscopy (AFM), Bacillus cereus, decontamination, plasma torch, scanning electron microscopy (SEM).

Rapid and specific recognition of methylphosphonic acid (MPA), the degradation product of nerve agents sarin, soman, VX, etc., was achieved with potentiometric measurements using a chemical sensor fabricated by a surface imprinting technique coupled with a nanoscale transducer, indium tin oxide (ITO). An octadecylsiloxane thin layer was covalently bound to the ITO-coated glass surface in the presence of MPA. After extraction of MPA, potentiometric measurements showed selective detection of MPA. The selectivity of the sensor has been tested on other alkylphosphonic acids, such as ethylphosphonic acid and propylphosphonic acid, as well as tert-butylphosphonic acid. The viability of the sensor in the presence of other chemical analogues, such as organophosphorus pesticides and herbicides, was investigated.

The concept of an ion-sensitive hydrogel ionic reservoir is demonstrated for hydrogel particles of three different size ranges. On the basis of the experimental results, a two-step mechanism affecting the kinetics of proton uptake into the hydrogel particles with ionizable groups is proposed, first being the fast binding of ions to the immediate surface of each particle and second, a slower successive diffusion of bound sites into the nest inner layer of polymer network.