Modeling flotation separation in a semi-batch process

A model for a semi-batch flotation separation process has been developed, based on available microprocess probabilities, and compared to experimental data obtained using a WEMCO laboratory flotation cell. In general, the model predicts the correct experimental trends. In many cases, the model also predicts removal efficiency very well. Parametric studies reveal that the model predictions are sensitive to a stability parameter, the turbulent energy density in the flotation cell, the contact angle between the solid particle and fluid, and the ratio of initial-to-critical film thickness.     

First Identification of a Putative Sex Pheromone in a Praying Mantid

Praying mantids are models for a wide variety of behavioral, physiological, and ecological studies, and sex pheromones have been assumed to be important components of their biology. However, no mantid pheromone has ever been identified. We collected volatiles emitted by females of the mantid, Sphodromantis lineola, via solid phase microextraction (SPME). Mass spectral analysis revealed the collected volatiles to be a mixture of pentadecanal and tetradecanal. We prepared a synthetic mixture of these compounds, and found that males were both attracted to this mixture and stimulated to exhibit typical precopulatory behavior. We then examined male antennae with scanning electron microscopy, and confirmed the presence of porous antennal sensilla typical of insect pheromone receptors, i.e., that male mantids are equipped with the appropriate morphological apparatus to receive volatile chemical signals. Pheromones, in conjunction with visual and tactile cues, are thus an important feature of the reproductive biology of this, and undoubtedly other species of mantids. In addition to adding a crucial aspect of behavioral biology to our knowledge of this group, identification and synthesis of mantid pheromones may be a first step in attracting and aggregating these generalist predators for use in pest control.     

Caffeine selectivity of divinylbenzene crosslinked polymers in aqueous media

The selective binding of caffeine to polymers is of interest in developing caffeine-specific sensors. The influence of the nature and quantity of crosslinking agents and functional monomers on the selectivity and binding affinity of a polymer to caffeine is reported. A high binding affinity and selectivity of divinylbenzene (DVB) crosslinked polymers toward caffeine was exhibited by the binding competition of caffeine with several dimethylated and chlorinated xanthines and N-methylated uric acids in aqueous media. To understand the nature of the caffeine–polymer interaction, we performed binding studies with solvents of different polarities and ionic strengths. The binding properties of DVB-based polymers containing different functional monomers were compared with Amberlite^® XAD resins. Analytes with hydrophilic and electron-withdrawing groups lowered their binding affinity with the polymer in comparison with caffeine and its dimethylated derivatives. The caffeine–polymer interaction appeared to be predominantly a hydrophobic π–π interaction but partly due to the presence of caffeine-specific sites. The reversibility of the caffeine–polymer binding was investigated, and the dissociation constants were approximated to be 27 and 6 mM. Dipole moments of caffeine and related molecules were estimated theoretically and were correlated with their corresponding B/T ratio, which is defined as the fraction of caffeine bound to the polymer. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 195–205, 2001     

Greenhouse gas emissions in an agroforestry system of the southeastern USA

Agroforestry systems may provide diverse ecosystem services and economic benefits that conventional agriculture cannot, e.g. potentially mitigating greenhouse gas emissions by enhancing nutrient cycling, since tree roots can capture nutrients not taken up by crops. However, greenhouse gas emission data from agroforestry systems are not available in the southeastern USA, thus limiting our ability to optimize agroforestry management strategies for the region. We hypothesized that tree-crop interactions could prevent excess N from being released to the atmosphere as nitrous oxide (N₂O). We determined N₂O and carbon dioxide (CO₂) emissions, soil temperature, water content, and surface-soil inorganic N in an 8-year-old agroforestry site at the Center for Environmental Farming Systems in Goldsboro, North Carolina, USA. The experimental design was a factorial arrangement of soil texture (loamy sand, sandy loam, and clay loam) and canopy cover (cropped alley, margin between crops and trees, and under Pinus palustris, Pinus taeda, and Quercus pagoda) with three replications. Sampling occurred 42 times within a year using static, vented chambers exposed to the soil for 1-h periods. Soil N₂O emission was lower under tree canopies than in cropped alleys, and margin areas were intermediate. Soil texture, water content, and inorganic N were key determinants of the magnitude of N₂O emission. Soil CO₂ emission was controlled by temperature and water content as expected, but surprisingly not by their interaction. Soil temperature was 1.8 ± 1.3 °C lower and soil water content was 0.043 ± 0.15 m³ m^?3 lower under tree canopy than in cropped alleys, which helped to reduce CO₂ emission under trees relative to that in cropped alleys. Our results provide a foundation for reducing greenhouse gas emissions in complex agricultural landscapes with varying soil texture by introducing timber production without abandoning agricultural operations.     

Combined Extraction of Cesium and Strontium from Alkaline Nitrate Solutions

Abstract

The combined extraction of cesium and strontium from caustic wastes can be achieved by adding a crown ether and a carboxylic acid to the Caustic‐Side Solvent Extraction (CSSX) solvent. The ligand 4,4′(5′)‐di(tert‐butyl)cyclohexano‐18‐crown‐6 and one of four different carboxylic acids were combined with the components of the CSSX solvent optimized for the extraction of cesium, allowing for the simultaneous extraction of cesium and strontium from alkaline nitrate media simulating alkaline high level wastes present at the U.S. Department of Energy Savannah River Site. Extraction and stripping experiments were conducted independently and exhibited adequate results for mimicking waste simulant processing through batch contacts. The promising results of these batch tests showed that the system could reasonably be tested on actual waste.     

An Ultrafine,Water-Based Condensation Particle Counter and its Evaluation under Field Conditions

An ultrafine, water-based condensation particle counter (U-WCPC, TSI Model 3786) has been compared to a butanol-based ultrafine counter (U-BCPC, TSI Model 3025) for measurement of atmospheric and freeway-tunnel aerosols. The U-WCPC utilizes a warm, wet-walled growth tube to activate and grow particles through water condensation in a laminar-flow. It has an aerosol sampling rate of 0.3 L/min, and a nominal detection limit near 3 nm. Several field comparisons were made to the butanol-based instrument with the same nominal detection limit. For measurements of size-selected aerosols with diameters of 5 nm and larger the two instruments generally agreed, with a mean response within 5%. At 3 nm particle size differences were observed, and these differences varied with the data set. Measurements of ambient aerosol in Boulder, Colorado showed higher counting efficiency at 3 nm with the U-BCPC, while in a California freeway tunnel the opposite trend was observed, with higher counting efficiencies at 3 nm observed by the U-WCPC. For direct measurement of atmospheric aerosols, the two types of instruments yielded equivalent concentrations, independent of particle number concentration.     

Graft polymerization of acrylonitrile onto starch‐coated polyethylene film surfaces

Starch‐coated polyethylene (PE) films were prepared by immersing PE in a hot, jet cooked solution of starch. They were allowed to react with acrylonitrile (AN) in the presence of ceric ammonium nitrate initiator, and the graft polymerization that occurred produced starch‐g‐polyacrylonitrile (PAN) coatings that contained about 25 wt % grafted PAN. The starch‐g‐PAN coatings tightly adhered to the PE film surfaces. When grafted starch coatings were wetted with water and the surfaces vigorously rubbed, less than 20% of the coating was removed. The fact that PAN‐grafted coatings were not removed with boiling water provided further evidence for their strong adherence. When starch was removed from the coating by acid hydrolysis, the residual grafted PAN still remained adsorbed on the PE surface. Because the grafted coating was completely removed by treatment with refluxing 0.7N sodium hydroxide, there is apparently no chemical bonding between starch‐g‐PAN and PE. The dimensional changes associated with the evaporation of water from these PAN‐grafted coatings caused the films to curl during drying. Because the final shape of these coated films depends upon the presence or absence of water in the surrounding environment, these films may be considered to be a type of stimulus‐responsive polymer. Attempts to graft polymerize methyl methacrylate and methyl acrylate onto starch‐coated PE surfaces, under conditions similar to those used with AN, were unsuccessful. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3323–3328, 2003     

Increasing Wet Green Strength of Alumina Body During Microfabrication by Colloidal Isopressing

Colloidal Isopressing involves formulating a slurry with a weakly attractive particle network that can be pre-consolidated to a high relative density by pressure filtration and still retain fluid-like characteristics. The pre-consolidated slurry is injected into an elastomeric mold and isopressed. Isopressing rapidly converts the slurry into an elastic body that can be removed from the mold without shape distortion. Not only is this process rapid, but since the water saturated compact produced by this method does not shrink during drying, it can also be converted into a green body without a long drying period. It is demonstrated that micron-size surface features, such as 5 μm wide channels with a depth/width ratio of 2, can be rapidly produced on the surface of alumina powder compacts. The fracturing of thin vertical portions of a micro-patterned surface during pressure release and demolding has been an obstacle to obtaining micron-sized features with high aspect ratios. A method is shown here that enables the fabrication of such features by strengthening the saturated isopressed body. It is shown that concentration controlled gelation of a poly(vinyl alcohol)–Tyzor^® Triethanolamine Tritanate (TE) additive effectively increases the strength of the elastic, isopressed body, saturated with water, while maintaining the low viscosity of the pre-consolidated slurry, which is required for transferring the pre-consolidated slurry into a rubber mold prior to isopressing.     

Rational Optimization of Dihydropyrimidinone-Quinoline Hybrids as Plasmodium falciparum Glutathione Reductase Inhibitors

A series of dihydropyrimidinone-based antimalarial compounds were designed and synthesised based on the previously identified amide-based quinoline hybrids which showed good resistance reversal ability against the resistant strain of Plasmodium falciparum. The aromatic ring on the dihydropyrimidinone of the original hits was exchanged for a methyl group to bring the molecular weights below 500 Da and also determine the effect of the aromatic ring count on the resistance reversal ability of the hybrids. Apart from the previously used amide bond, the hybrid linker was also extended to the triazole linker. Although the triazole linker is synthetically easier to access, the use of an amide linker seems to have an activity advantage. The synthesised compounds in addition to the previously identified hits were subjected to molecular docking particularly targeting the orthosteric site of Plasmodium falciparum glutathione reductase (PfGR) protein. The ligand with the best binding interaction was rationally optimised to increase its suitability as a competitive inhibitor against the cofactor of the PfGR. Two of the optimised ligands showed better binding affinities than the cofactor while one of the two ligands displayed hydrophobically packed correlated hydrogen-bond which is very important in maintaining the ligand stability within the protein. In silico ADME predictions of the synthesised compounds indicate that these compounds possess good pharmacokinetic properties.     

On the use of large time steps with ELLAM for transport with kinetic reactions over heterogeneous domains

An Eulerian Lagrangian localized adjoint method (ELLAM) is considered for the resolution of advection‐dominated transport problems in porous media. Contrary to standard Eulerian methods, ELLAM can use large time steps because the advection term is approximated accurately without any CFL restriction. However, it is shown in this article that special care must be taken for the approximation of the dispersive and reactive terms when large time steps are used over heterogeneous domains. An alternative procedure is proposed. It is based on an equivalent dispersion coefficient or an equivalent reaction rate when different zones are encountered during the tracking. Numerical experiments are performed with variable dispersion or variable reaction rates over space (including nonlinearity). When classical ELLAM require numerous time steps to handle heterogeneity, the alternative procedure is shown to perform with the same accuracy in a single time step. © 2009 American Institute of Chemical Engineers AIChE J, 2009