Kinetics and isotherm studies for the adsorption of boron from water using titanium dioxide

Boron is a necessary element for plants that are generally found in the ground and seawater, but it can also be poisonous in large doses. Contamination of water with boric acid or borate ions is a global concern. Due to the absence of the chemical charge that boron possesses, its removal is often difficult. To investigate boron's adsorption characteristics, kinetic, isotherm, and isothermal studies were performed. The adsorption of boron was shown to be a pH-dependent mechanism, with the best results at around pH 9.0. About 47% of the boron from a solution of 50 mg L⁻¹ was removed using 5 g titanium dioxide in 30 min. It was also demonstrated that boron adsorption kinetics increased with temperature, which is best described by the pseudo-second-order kinetic model (R² > 0.98) and also fits well with Elovich and pseudo-first-order models (R² > 0.94) at pH 9.0. Equilibrium was reached in about 40 min for all the samples. The film boundary layer diffusion step limits the rate. Experimental results correspond well to the Freundlich isotherm (R² = 0.95–0.99). Langmuir and Temkin's isotherms also fitted reasonably well (R² = 0.94–0.98). The Freundlich and Langmuir constants indicate favourable adsorption. The Gibbs free energy (ΔG) values increased negatively (from −11.47 to −15.63 kJ mol⁻¹) with increasing temperature, signifying a feasible and spontaneous process. The enthalpy change (ΔH) value of about 30.35 kJ mol⁻¹ indicated endothermic physical adsorption. The results indicate that titanium dioxide is an excellent and safe adsorbent for the removal of boron from water.     

DC Link Filter Design Considerations in Three-Phase Voltage Source Inverter-Fed Induction Motor Drive System

The dc link filter elements in a three-phase voltage source inverter-fed induction motor system can affect the performance of the drive system if not properly chosen. The requirements, design considerations, and a simplified procedure for the selection of filter component values based on minimization of voltage and current ripple currents in the dc link, damping effects, and on resonant frequency considerations are formulated. Typical computational results and experimental waveforms are presented.     

Graph theory augmented math programming approach to identify minimal reaction sets in metabolic networks

Bioprocesses are of growing importance as an avenue to produce chemicals. Microorganisms containing only desired catalytic and replication capabilities in their metabolic pathways are expected to offer efficient processes for chemical production. Realizing such minimal cells is the holy grail of metabolic engineering. In this paper, we propose a new method that combines graph-theoretic approaches with mixed-integer liner programming (MILP) to design metabolic networks with minimal reactions. Existing MILP based computational approaches are computationally complex especially for large networks. The proposed graph-theoretic approach offers an efficient divide-and-conquer strategy using the MILP formulation on sub-networks rather than considering the whole network monolithically. In addition to the resulting improvement in computational complexity, the proposed method also aids in identifying the key reactions to be knocked-out in order to achieve the minimal cell. The efficacy of the proposed approach is demonstrated using three case studies from two organisms, Escherichia coli and Saccharomyces cerevisiae.     

Synthesis of boron/nitrogen substituted carbons for aqueous asymmetric capacitors

Boron/nitrogen substituted carbons were synthesized by co-pyrolysis of polyborazylene/coal tar pitch blends to yield a carbon with a boron and nitrogen content of 14 at% and 10 at%, respectively. The presence of heteroatoms in these carbons shifted the hydrogen evolution overpotential to −1.4 V vs Ag/AgCl in aqueous electrolytes, providing a large electrochemical potential window (∼2.4 V) as well as a specific capacitance of 0.6 F/m². An asymmetric capacitor was fabricated using the as-prepared low surface area carbon as the negative electrode along with a redox active manganese dioxide as the positive electrode. The energy density of the capacitor exceeded 10 Wh/kg at a power density of 1 kW/kg and had a cycle life greater than 1000 cycles.     

Electrochemical copolymerization and characterization of aniline and isoprene in aqueous p‐toluene sulfonic acid solution

Uniform and adherent copolymer coating of poly(aniline‐co‐isoprene) was successfully formed on low‐carbon‐steel electrodes by potentiostatic electropolymerization. Electropolymerization was performed by using aqueous p‐toluene sulfonic acid solution as electrolyte. Applied potential and feed ratios of monomers (aniline and isoprene) were systematically varied and the reactions were done under aqueous conditions. The copolymer coatings were characterized by infrared spectroscopy and the formation of copolymer was confirmed by the presence of aliphatic secondary amine, aromatic secondary amine, and aliphatic CH stretch groups. The electronic structure of the copolymers was further investigated by using UV/Vis absorption spectroscopy. The electrochemistry of the formation of copolymers was studied by using cyclic voltammetry. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 184–192, 2002; DOI 10.1002/app.10298     

Starch urea formaldehyde matrix encapsulation of solid agrochemicals. I. Matrix synthesis and characterizations

A starch urea formaldehyde (starch-UF) matrix has been studied for application to the encapsulation of a solid insecticide. The pertinent parameters relating to the matrix synthesis have been identified and the influences of these parameters on release of the insecticide from the starch UF matrix have been investigated. The key parameter controlling the rate of release is the urea to starch ratio. It is shown that the release process can be described in terms of the generalized equation M_t/M_∞ = ktⁿ where k and n vary with system variables.     

In situ TEM study of microplasticity and Bauschinger effect in nanocrystalline metals

In situ transmission electron microscopy straining experiments with concurrent macroscopic stress–strain measurements were performed to study the effect of microstructural heterogeneity on the deformation behavior of nanocrystalline metal films. In microstructurally heterogeneous gold films (mean grain size d_m = 70 nm) comprising randomly oriented grains, dislocation activity is confined to relatively larger grains, with smaller grains deforming elastically, even at applied strains approaching 1.2%. This extended microplasticity leads to build-up of internal stresses, inducing a large Bauschinger effect during unloading. Microstructurally heterogeneous aluminum films (d_m = 140 nm) also show similar behavior. In contrast, microstructurally homogeneous aluminum films comprising mainly two grain families, both favorably oriented for dislocation glide, show limited microplastic deformation and minimal Bauschinger effect despite having a comparable mean grain size (d_m = 120 nm). A simple model is proposed to describe these observations. Overall, our results emphasize the need to consider both microstructural size and heterogeneity in modeling the mechanical behavior of nanocrystalline metals.     

Nanoenergetic Composites of CuO Nanorods,Nanowires, and Al‐Nanoparticles

This paper reports on the synthesis of the nanoenergetic composites containing CuO nanorods and nanowires, and Al‐nanoparticles. Nanorods and nanowires were synthesized using poly(ethylene glycol) templating method and combined with Al‐nanoparticles using ultrasonic mixing and self‐assembly methods. Poly(4‐vinylpyridine) was used for the self‐assembly of Al‐nanoparticles around the nanorods. At the optimized values of equivalence ratio, sonication time, and Al‐particle size, the combustion wave speed of 1650 m s⁻¹ was obtained for the nanorods‐based energetics. For the composite of nanowires and Al‐nanoparticles the speed was increased to 1900 m s⁻¹. The maximum combustion wave speed of 2400 m s⁻¹ was achieved for the self‐assembled composite, which is the highest known so far among the nanoenergetic materials. It is possible that in the self‐assembled composites, the interfacial contact between the oxidizer and fuel is higher and resistance to overall diffusional process is lower, thus enhancing the performance.     

Optimization of conditions for hydrogen production from complex dairy wastewater by anaerobic sludge using desirability function approach

Present study deals with the multiple-response optimization for biohydrogen production using anaerobic sludge and outstanding approach to overcome the drawbacks of conventional response surface methodology (RSM). Dairy wastewater was used as source in batch fermentation was followed for this study. Response surface methodology (RSM), based on a three level, four variable Box–Behnken design, was employed to obtain the best possible combination of substrate concentration, pH, COD/N ratio and COD/P ratio for maximum H₂ yield (HY) and specific hydrogen production rate (SHPR). Experimental data were evaluated by applying RSM integrating a desirability function approach. The optimum H₂ yield and SHPR conditions were: substrate concentration 15.3 g COD/L, pH 5.5, COD/N ratio 100.5 and COD/P ratio 120 with maximum overall desirability D of 0.94. The confirmation experiment under these optimal condition showed a HY and SHPR of 13.54 mmol H₂/g COD and 29.91 mmol H₂/g-VSS.d, respectively. This was only 0.22% and 0.20%, respectively, different from the predicted values, suggesting that the desirability function approach with RSM was a useful technique to get the maximum H₂ yield and SHPR simultaneously.