Adsorption of mercury by carbonaceous adsorbents prepared from rubber of tyre wastes

Rubber from tyre wastes has been used to prepare carbonaceous adsorbents and the products obtained have been tested as adsorbents for mercury in aqueous solution. The adsorbents have been prepared by applying thermal, chemical and combined (thermal and chemical or vice versa) treatments. Tyre rubber has been: heated at 400 or 900 degrees C for 2 h in N2, chemically-treated with H2SO4, HNO3 or H2SO4/HNO3 solution for 24 h, and in two successive steps first heated at 400 degrees C for 2h in N2 and then treated with a H2SO4/HNO3 solution for 24 h, or vice versa. Resultant products have been characterised in terms of elementary composition and textural properties. The adsorption of mercury has been studied from kinetic and equilibrium standpoints. The treatments effected to tyre rubber decrease the carbon content and the hydrogen content. The oxygen content and the nitrogen content increase for the chemically-treated products. The heat treatment of tyre rubber results in a larger development of surface area, microporosity, and mesoporosity than the chemical treatments. These treatments, however, produce a great creation of macropores. In comparison to the starting rubber, the adsorption process of mercury is faster when the material is heated or treated with the H2SO4, HNO3 or 1:3 H2SO4/HNO3 solution. These adsorbents are either a non-porous solid or possess a high mesopore volume or a wide pore size distribution in the macropore range. The adsorption capacity is larger for products prepared by heat, chemical and combined treatments of the rubber. A common textural characteristic of these adsorbents is their better developed microporosity. The ability to adsorb mercury is higher for the heated products than for the chemically-treated ones. The maximum adsorption of mercury is 211 mg g(-1). The constant Kf of the Freundlich equation is as high as 108.9 mg g(-1).     

5-Hydroxytryptophan as a precursor of a catalyst for the oxidation of NADH

Following oxidation of 5-hydroxytryptophan (5-HTPP) at a pyrolytic graphite electrode at pH 7.5, two quasi-reversible redox couples emerge at -0.170 and +0.032 V, respectively, due to oxidation products strongly adsorbed to the electrode surface. These redox processes have been electrochemically and kinetically characterized in terms of the dependence of the formal potential (E degrees ') with pH, variation of the current density with scan rate, operational stability, and electron-transfer rate constant (k(s)). The wave centered at +0.032 V could mediate the oxidation of NADH, exhibiting a strong and persistent electrocatalytic response. A quinone-imine structure has been proposed as the electrocatalytically active species. The kinetics of the reaction between the mediator and NADH has been characterized via rotating disk electrode voltammetry, and it has been found that the rate constant for the reaction is dependent on the solution concentration of NADH. 5-HTPP modified electrodes could be employed in the amperometric detection of NADH with a limit of detection in the nanomolar range. Moreover, 5-HTPP modified electrodes retain their electrocatalytic activity for at least one week. The potential application of these electrodes to amperometric biosensor is demonstrated.     

Self-association behaviour of protein:surfactant systems in alcohol/water mixtures

The effect of the addition of short-chain monohydric alcohols (ethanol and propan-2-ol) to the protein:surfactant system lysozyme:sodium dodecyl sulfate (Lz:SDS) in aqueous solution was investigated using a conductometric technique. A second protein:surfactant system, bovine serum albumin:SDS (BSA:SDS) was also investigated so that the effect of a different protein conformation and composition could be compared. The critical aggregation concentration (CAC) of the protein forming the complex and the critical micelle concentration (CMC *) of SDS in the presence of protein, at different alcohol concentrations, were determined. It was found in both cases that the addition of alcohol does not produce a significant change in the CAC, whereas the CMC * displays variation with alcohol concentration that shows an inversion in the ranges 0.05-0.06 ethanol mole fraction and 0.02-0.03 propan-2-ol mole fraction. This suggests that, in contrast with the CAC behaviour, the major factor that drives SDS micellization in the presence of protein is the variation in water structure. Results also suggest that it occurs in the same way for both proteins, where electrostatic interactions are the main force in the formation of the complex. Conversely, hydrophobic interactions play the dominant role at the micellization stage, and only the extent of the interaction between protein:surfactant aggregates and surfactant species seems to depend on protein nature.     

Clarifications to the paper "Holographic characteristics of a 1-mm-thick photopolymer to be used in holographic memories"

We have corrected typing errors related to the characterization of the dynamic range of the acrylamide photopolymer described in an earlier study [Appl. Opt. 42, 7008 (2003)]. The M number is expressed as M/# instead of M# as appears in the text. The value calculated from the experimental results that are included in the article is M/# = 3.8 instead of 38 as appears in the text.     

The efficiency of potassium removal during bicarbonate hemodialysis

Patients on chronic hemodialysis often portray high serum [K+]. Although dietary excesses are evident in many cases, in others, the cause of hyperkalemia cannot be identified. In such cases, hyperkalemia could result from decreased potassium removal during dialysis. This situation could occur if alkalinization of body fluids during dialysis would drive potassium into the cell, thus decreasing the potassium gradient across the dialysis membrane. In 35 chronic hemodialysis patients, we compared two dialysis sessions performed 7 days apart. Bicarbonate or acetate as dialysate buffers were randomly assigned for the first dialysis. The buffer was switched for the second dialysis. Serum [K+], [HCO3-], and pH were measured in samples drawn before dialysis; 60, 120, 180, and 240 min into dialysis; and 60 and 90 min after dialysis. The potassium removed was measured in the dialysate. During the first 2 hr, serum [K+] decreased equally with both types of dialysates but declined more during the last 2 hr with bicarbonate dialysis. After dialysis, the serum [K+] rebounded higher with bicarbonate bringing the serum [K+] up to par with acetate. The lower serum [K+] through the second half of bicarbonate dialysis did not impair potassium removal (295.9 +/- 9.6 mmol with bicarbonate and 299.0 +/- 14.4 mmol with acetate). The measured serum K+ concentrations correlated with serum [HCO3-] and blood pH during bicarbonate dialysis but not during acetate dialysis. Alkalinization induced by bicarbonate administration may cause redistribution of K during bicarbonate dialysis but this does not impair its removal. The more marked lowering of potassium during bicarbonate dialysis occurs late in dialysis, when exchange is negligible because of a low gradient.     

Invariant pattern recognition by use of wavelength multiplexing

Rotation-invariant pattern recognition can be achieved with circular-harmonic decomposition. A common problem with such a filter is that, because it is only a single term out of the circular decomposition, it does not contain much of the reference object's energy. Thus, the obtained correlation selectivity is low. This problem is solved by use of wavelength multiplexing. First, different harmonic terms are encoded by different wavelengths, and then they all are added incoherently in the output correlation plane. This process leads to rotation-invariant pattern recognition with a higher discrimination ability.     

Analysis of the resonant scattering of light by cylinders at oblique incidence

We study the resonant scattering of light at oblique incidence by dielectric uncoated and coated cylinders. We develop a stable algorithm that permits us to calculate the resonances of a single dielectric cylinder as the tilting angle varies. This algorithm is based on semiclassical formulas for the distance between resonances. Results show that the resonances and the resonant electromagnetic energy flux near and internal to the cylindrical surface are highly sensitive to variations in the tilting angle. In addition, the coating effects are studied for scattering of light at oblique incidence by an infinite, perfect cylindrical conductor coated by a dielectric layer. In this case the resonance calculations show a peculiar similarity between this light scattering and atomic-molecular scattering. A physical interpretation for these effects is given, based on an analogy of optics and quantum mechanics.     

Dynamic holographic moiré patterns in photorefractive Bi12TiO20 and small-angle measurements

A procedure for obtaining real-time holographic moirélike patterns and measuring small angles is proposed. Two rotated sinusoidal phase gratings are superposed, and the result represents a promising technique for making small-angle measurements in metrological applications. The experiments are performed with a diffusion-only recording mechanism in the photorefractive crystal Bi(12)TiO(20) illuminated by lambda = 0.633 mum light from a He-Ne laser.     

Rotation-invariant optical recognition of three-dimensional objects

An automatic method for rotation-invariant three-dimensional (3-D) object recognition is proposed. The method is based on the use of 3-D information contained in the deformed fringe pattern obtained when a grating is projected onto an object's surface. The proposed method was optically implemented by means of a two-cycle joint transform correlator. The rotation invariance is achieved by means of encoding with the fringe pattern a single component of the circular-harmonic expansion derived from the target. Thus the method is invariant for rotations around the line of sight. The whole experimental setup can be constructed with simple equipment. Experimental results show the utility of the proposed method.     

Software architecture for multi-bed FDK-based reconstruction in X-ray CT scanners

Most small-animal X-ray computed tomography (CT) scanners are based on cone-beam geometry with a flat-panel detector orbiting in a circular trajectory. Image reconstruction in these systems is usually performed by approximate methods based on the algorithm proposed by Feldkamp et al. (FDK). Besides the implementation of the reconstruction algorithm itself, in order to design a real system it is necessary to take into account numerous issues so as to obtain the best quality images from the acquired data. This work presents a comprehensive, novel software architecture for small-animal CT scanners based on cone-beam geometry with circular scanning trajectory. The proposed architecture covers all the steps from the system calibration to the volume reconstruction and conversion into Hounsfield units. It includes an efficient implementation of an FDK-based reconstruction algorithm that takes advantage of system symmetries and allows for parallel reconstruction using a multiprocessor computer. Strategies for calibration and artifact correction are discussed to justify the strategies adopted. New procedures for multi-bed misalignment, beam-hardening, and Housfield units calibration are proposed. Experiments with phantoms and real data showed the suitability of the proposed software architecture for an X-ray small animal CT based on cone-beam geometry.