Single-Shot Characterization of Enzymatic Reaction Constants K(m) and k(cat) by an Acoustic-Driven, Bubble-Based Fast Micromixer

In this work we present an acoustofluidic approach for rapid, single-shot characterization of enzymatic reaction constants K(m) and k(cat). The acoustofluidic design involves a bubble anchored in a horseshoe structure which can be stimulated by a piezoelectric transducer to generate vortices in the fluid. The enzyme and substrate can thus be mixed rapidly, within 100 ms, by the vortices to yield the product. Enzymatic reaction constants K(m) and k(cat) can then be obtained from the reaction rate curves for different concentrations of substrate while holding the enzyme concentration constant. We studied the enzymatic reaction for β-galactosidase and its substrate (resorufin-β-D-galactopyranoside) and found K(m) and k(cat) to be 333 ± 130 μM and 64 ± 8 s(-1), respectively, which are in agreement with published data. Our approach is valuable for studying the kinetics of high-speed enzymatic reactions and other chemical reactions.     

Feasibility study of a solar chimney power plant in Jordan

A solar chimney power plant system is theoretically designed for future erection in Jordan. Analytical analysis of the system is simulated by mathematical software. The actual values of solar irradiation in Jordan are used in the simulation to predict the power output of the solar chimney power plant. The output results of the maximum (inlet) values of velocity, pressure, and mass flow rate of air versus the chimney height variation are obtained. Furthermore, the electrical power output and the efficiency of chimney versus chimney height variation were determined. For a solar collector diameter of 40 m and a chimney diameter of 3.5 m, the maximum power output (85 kW) was obtained for a chimney height of 210 m.     

A reaction mechanism for gasoline surrogate fuels for large polycyclic aromatic hydrocarbons

This work aims to develop a reaction mechanism for gasoline surrogate fuels (n-heptane, iso-octane and toluene) with an emphasis on the formation of large polycyclic aromatic hydrocarbons (PAHs). Starting from an existing base mechanism for gasoline surrogate fuels with the largest chemical species being pyrene (C₁₆H₁₀), this new mechanism is generated by adding PAH sub-mechanisms to account for the formation and growth of PAHs up to coronene (C₂₄H₁₂). The density functional theory (DFT) and the transition state theory (TST) have been adopted to evaluate the rate constants for several PAH reactions. The mechanism is validated in the premixed laminar flames of n-heptane, iso-octane, benzene and ethylene. The characteristics of PAH formation in the counterflow diffusion flames of iso-octane/toluene and n-heptane/toluene mixtures have also been tested for both the soot formation and soot formation/oxidation flame conditions. The predictions of the concentrations of large PAHs in the premixed flames having available experimental data are significantly improved with the new mechanism as compared to the base mechanism. The major pathways for the formation of large PAHs are identified. The test of the counterflow diffusion flames successfully predicts the PAH behavior exhibiting a synergistic effect observed experimentally for the mixture fuels, irrespective of the type of flame (soot formation flame or soot formation/oxidation flame). The reactions that lead to this synergistic effect in PAH formation are identified through the rate-of-production analysis.     

Numerical heat transfer study for a large rubber product

The physical processes of heat transfer are typically complicated in the curing of rubber. In this study, the image plot and the plot of the temperature profile were obtained in such an environment, and then compared with the finite element method (FEM), which is used in finite element analysis (FEA) software. A good agreement was observed, and the difference was less than 1% when evaluating the different curing conditions. This confirms that the correct curing time can be determined by studying the temperature profile, which will help to avoid the deterioration of the mechanical properties of thick rubber products.     

Development of a pH-responsive imprinted polymer for diclofenac and study of its binding properties in organic and aqueous media

Three different molecularly imprinted polymers (MIPs) for drug delivery of diclofenac in gastrointestinal tract were synthesized employing bulk polymerization method and their binding and release properties were studied in different pH values. Methacrylic acid (MAA), methacrylamide (MAAM) and 4-vinyl pyridine (4VP) were tested as functional monomers and ethylene glycole dimethacrylate (EDMA) was used as a cross-linker monomer in polymeric feed. Binding properties and imprinting factor (IF) of MIPs were studied in comparison with their non-imprinted ones (Blank) in organic and aqueous media. Diclofenac release in aqueous solvents at pH values of 1.5, 6.0 and 8.0, simulating gastrointestinal fluids, were also studied. The results indicated the specific binding of diclofenac to imprinted polymers. Duo to the stronger non-specific bounds in aqueous solutions, IF values decreased in water compared to acetonitrile as an organic medium. Our results proved that all polymers represented pH-responsive diclofenac delivery at above conditions. The data showed that imprinted polymer, prepared by MAA had superior properties, in comparison with other polymers, for minimum release (14%) of drug in gastric acid and maximum release (90%) in basic condition. The results indicated that diclofenac imprinted polymer could be used as a pH-responsive matrix in preparation of a new drug delivery system for diclofenac.     

Thermodynamic and kinetic studies for the adsorption of Hg(II) by nano-TiO2 from aqueous solution

Titanium dioxide nanocrystals were employed, for the first time, for the sorption of Hg(II) ions from aqueous solutions. The effects of varying parameters such as pH, temperature, initial metal concentration, and contact time on the adsorption process were examined. Adsorption equilibrium was established in 420 min and the maximum adsorption of Hg(II) on the TiO₂ was observed to occur at pH 8.0. The adsorption data correlated with Freundlich, Langmuir, Dubinin–Radushkevich (D–R), and Temkin isotherms. The Freundlich isotherm showed the best fit to the equilibrium data. The Pseudo-first order and pseudo-second-order kinetic models were studied to analyze the kinetic data. A second-order kinetic model fit the data with the (k₂ = 2.8126 × 10^?3 g mg^?1min^?1, 303 K). The intraparticle diffusion models were applied to ascertain the rate-controlling step. The thermodynamic parameters (ΔG°, ΔH°, and ΔS°) were calculated which showed an endothermic adsorption process. The equilibrium parameter (R_L) indicated that TiO₂ nanocrystals are useful for Hg(II) removal from aqueous solutions.     

Chaos Synchronization in Josephson Junctions

In this paper, we have discussed the application of new nonlinear recursive controllers on Josephson junction (JJ) chaotic systems. Controlling bifurcation as well as chaos has been rapidly advancing in the last decade. Thus, emphasis has been placed on control design techniques which result in prescribed nonlinear performance dynamics for practical controlled processes. This study has shown that a nonlinear recursive controller is effective in controlling an undesirable JJ chaotic behavior. In addition to that, the synchronization of two JJ chaotic nonlinear dynamical systems can be used to advantage in communication systems. In fact, communication security is promising through chaos. Using nonlinear control method, we have demonstrated that it is possible to achieve synchronization in electronic circuits such as JJ. The study showed the effectiveness of the designed controller in communication signal synchronization. For the purpose of verification and comparison, we designed a control signal based on master and slave concept.     

Nanofork for single cells adhesion measurement via ESEM-nanomanipulator system

In this paper, single cells adhesion force was measured using a nanofork. The nanofork was used to pick up a single cell on a line array substrate inside an environmental scanning electron microscope (ESEM). The line array substrate was used to provide small gaps between the single cells and the substrate. Therefore, the nanofork could be inserted through these gaps in order to successfully pick up a single cell. Adhesion force was measured during the cell pick-up process from the deflection of the cantilever beam. The nanofork was fabricated using focused ion beam (FIB) etching process while the line array substrate was fabricated using nanoimprinting technology. As to investigate the effect of contact area on the strength of the adhesion force, two sizes of gap distance of line array substrate were used, i.e., 1 μm and 2 μm. Results showed that cells attached on the 1 μm gap line array substrate required more force to be released as compared to the cells attached on the 1 μm gap line array substrate.