An iron-based T 1 contrast agent made of iron-phosphate complexes: In vitro and in vivo studies

A new iron-based T ₁ contrast agent consisting of a complex of iron ions coordinated to phosphate and amine ligands (Fe_(phos) in short) has been characterized by spectroscopic and magnetic measurements. NMR relaxation studies showed r ₁ values to be dependent on the phosphate salt concentration, K₂HPO₄, present in the medium. r ₁ reaches a maximum value of 2.5 mM^?1 s^?1 for measurements carried out at 7 T and 298 K. ³¹P MRS, Mössbauer spectroscopy and magnetic measurements of Fe_(phos) solutions suggest paramagnetic Fe³⁺ ions present in the studied iron–phosphate complex. In vitro and in vivo toxicity experiments with C6 cells and CD1 mice, respectively, demonstrated lack of toxicity for Fe_(phos) at the highest dose tested in the MRI experiments (12 mM iron for C6 cells and 0.32 mmol iron/kg for mice). Finally, T ₁ weighted images of brain tumours in mice have shown positive contrast enhancement of Fe_(phos) for tumour afflicted regions in the brain.     

Determination of the complex permittivity of cherry,pulped, green,and roasted coffee using a planar dielectric platform and a coaxial probe between 0.3 and 6 GHz

The complex permittivity for four processing stages of coffee: coffee cherries, pulped coffee, green coffee, and roasted coffee was obtained and divided into two groups. The wet group is constituted by cherry and pulped coffee, and the dry group by green and roasted coffee. The wet group presented a dielectric constant between 64 and 43, and a loss factor between 34 and 12. The dry group has values oscillating between 1.55 and 1.1 for the dielectric constant, and 0.037 and 0.005 for the loss factor. The permittivity difference between the wet and dry groups suggests the dependence of the coffee permittivity on the water content, along with the presence of other polar compounds. A decaying response for the dielectric constant was seen, with a proportion of 30:1 from the wet to the dry group. The loss factor presents a convex response for the wet group and a constant response for the dry group with a factor of 500 to a 100:1 from the wet to the dry group. A set of 18 samples at every stage was used to estimate the moisture content by partial least squares. The Meyer and Schilz coefficient was used for these models, that resulted in prediction errors of 2.8% and 3.8% when compared to the stage mean moisture content for the wet group. The dry group resulted in errors of 21% and 89.7%. These results indicate that the complex permittivity of coffee is capable of estimating physicochemical variables as the moisture content of the beans at distinct processing stages.     

Flywheel energy storage systems: Review and simulation for an isolated wind power system

In flywheel based energy storage systems (FESSs), a flywheel stores mechanical energy that interchanges in form of electrical energy by means of an electrical machine with a bidirectional power converter. FESSs are suitable whenever numerous charge and discharge cycles (hundred of thousands) are needed with medium to high power (kW to MW) during short-time periods (seconds–minutes). Monitoring of the FESS state of charge is simple and reliable as only the spinning speed is needed. The materials for the flywheel, the type of electrical machine, the type of bearings and the confinement atmosphere which all together determine the FESSs energy efficiency (>85%) are reviewed. Main FESS applications: power quality, traction and aerospace are presented. Additionally in this paper it is presented the simulation of an isolated wind power system (IWPS) consisting of a wind turbine generator (WTG), a consumer load, a synchronous machine (SM) and a FESS. A low-speed iron flywheel driven by an asynchronous machine (ASM) is sized for the presented IWPS. The simulation results with graphs for system frequency, system voltage, active powers of the different elements, and FESS-ASM speed, direct and quadrature currents are presented showing that the FESS effectively smoothes the wind power and consumer load variations.     

Thermal-Microstructural Analysis of Anodic and Electrolytic Copper Solidification: Simulation and Experimental Validation

This work analyzes the solidification process of anodic and electrolytic copper. The aim of this study is to perform an experimental validation of numerical results computed using a proposed thermal formulation including microstructural evolution. To this end, a set of experiments is carried out testing primary and eutectic phase formation in copper. To evaluate the formation of different microstructural phases, anodic copper (99.80 pct purity, approximately) and electrolytic copper (99.99 pct purity, approximately) are used. Primary and eutectic phases evolve in anodic copper; meanwhile, only a primary phase is obtained in electrolytic copper. The effect of heat extraction conditions is evaluated using sand, graphite, and steel molds to promote different cooling rates. The proposed microstructural model takes into account nucleation and grain growth laws based on thermal undercooling together with microstructural evolution. The primary copper evolution model is based on solute diffusion at the grain scale and on the dendrite top-growing kinetic; meanwhile, the eutectic evolution is assumed proportional to the copper initial composition and eutectic undercooling. The corresponding numerical formulation is solved in the framework of the finite-element method. Finally, the computed temperature histories and final values for the grain density and radius, including primary or dendritic phase and eutectic solid volumetric fractions, are all compared and validated with the experimental measurements.     

Kinetics of L-tryptophan production from indole and L-serine catalyzed by whole cells with tryptophanase activity

The essential amino acid L-tryptophan can be produced by a condensation reaction between indole and L-serine, catalyzed by whole cells of Escherichia coli B1t-7A with tryptophanase activity. The reaction was previously studied using soluble tryptophanase, a kinetic mechanism proposed and the catalytic properties of the enzyme described. It is important, however, to determine the kinetic parameters of the reaction catalyzed by whole cells, if the process is to be designed with the catalyst in this form. The reaction stoichiometry was established, a mole of product being formed from a mole of each reactant, with no indication of side reactions under the conditions used. The two-substrate reaction kinetics were characterized and modelled, assuming an enzyme-substituted mechanism and no product inhibition. Theoretical consumption rates of indole were compared with experimental values obtained in a batch reactor system. The K(m) values of whole cells towards L-serine and indole were 1.79 M and 0.07 M, respectively. These values are, as expected, considerably higher than their counterparts for soluble tryptophanase.     

ATR-FTIR Study of the Decomposition of Acetic Anhydride on Fosfotungstic Wells–Dawson Heteropoly Acid Using Concentration-Modulation Excitation Spectroscopy

The decomposition of acetic anhydride in liquid phase on a fosfotungstic Wells–Dawson heteropoly acid (HPA) was investigated by in situ ATR-FTIR spectroscopy. Transient and concentration-modulation excitation spectroscopy (MES) experiments in combination with phase-sensitive detection (PSD) were used to monitor the solid–liquid interface. The MES method is based on the periodic variation of a parameter of the reaction media such as, the reactant concentration. That periodic alteration causes varying infrared signals of the surface adsorbed species that are subsequently demodulated with the PSD methodology. Thus, the separation of the static signals from the changing ones is achieved, and species with different response can be observed in the spectra. Using MES-PSD coupled with ATR-FTIR, acetic anhydride was observed to decompose to acetic acid, acetate and acyl [CH₃C(O)⁺] species, involving Brønsted acid sites of the HPA catalyst. The CH₃C(O)⁺ is a very unstable intermediate species and it is the key intermediate in the Friedel–Crafts acylation reactions. Moreover, the acetate groups are spectator species since remain strongly adsorbed on the catalyst surface and do not further react.     

High-Impact PLA in Compatibilized PLA/PCL Blends: Optimization of Blend Composition and Type and Content of Compatibilizer

In this work, the effectiveness of seven commercial compatibilizers is tested in polylactide (PLA)/poly(ε-caprolactone) (PCL) blends with different compositions to obtain a high-impact PLA. None of the compatibilizers is effective for 90/10 and 80/20 PLA/PCL compositions, as no improvement of the impact strength is observed. For the 70/30 composition, compatibilizers having glycidyl methacrylate (GMA) and acrylate groups in their structure are proved the most effective, as the morphological change towards co-continuity induced by them leads to significant impact strength improvements (of ≈345% and 90% with respect to the neat PLA and the noncompatibilized PLA/PCL 70/30 blend, respectively). The 70/30 PLA/PCL composition, as it shows the best balance of properties, and the best compatibilizer (ElvaloyPTW) are chosen to carry out the optimization of the compatibilizer content. It is found that adding 6 phr to the blend results in highly toughened and ductile blends while maintaining a high modulus and yield strength values. Larger compatibilizer contents lead to even higher impact strength values, but the low-strain mechanical properties are notably reduced. Thus, in this work, a simple and easily scalable method to produce high-impact PLA is shown, as it implies the compounding of three commercially available components without involving any toxic solvents.