Thermal evaluation of the use of porous ceramic plates on ventilated façades—part II: Thermal behavior

The effects of porous ceramic plates on the thermal behavior of ventilated façades were evaluated, and the results are presented herein. Thermal behavior in a ventilated façade of specimens containing 40 wt% of lime mud and a firing temperature of 1100°C was evaluated and compared with a commercial porcelain ceramic tile, which was the reference material. An experimental apparatus was designed to evaluate the thermal performance of the studied ventilated façades. The results revealed that the ventilated façade composed of the studied porous ceramic tiles produced a greater reduction in temperature between the external environmental and the interior of a box representing a building (ΔT5) of 65.7°C, compared with the façade composed of the commercial porcelain ceramic tiles (ΔT5 = 56.0°C) and even the traditional façade (ΔT5 = 49.1°C). Thus, porous ceramic tiles based on byproducts are promising candidates for ventilated façade systems.     

Iron Oxide Nanoparticles Employed as Seeds for the Induction of Microcrystalline Diamond Synthesis

Iron nanoparticles were employed to induce the synthesis of diamond on molybdenum, silicon, and quartz substrates. Diamond films were grown using conventional conditions for diamond synthesis by hot filament chemical vapor deposition, except that dispersed iron oxide nanoparticles replaced the seeding. X-ray diffraction, visible, and ultraviolet Raman Spectroscopy, energy-filtered transmission electron microscopy , electron energy-loss spectroscopy, and X-ray photoelectron spectroscopy (XPS) were employed to study the carbon bonding nature of the films and to analyze the carbon clustering around the seed nanoparticles leading to diamond synthesis. The results indicate that iron oxide nanoparticles lose the O atoms, becoming thus active C traps that induce the formation of a dense region of trigonally and tetrahedrally bonded carbon around them with the ensuing precipitation of diamond-type bonds that develop into microcrystalline diamond films under chemical vapor deposition conditions. This approach to diamond induction can be combined with dip pen nanolithography for the selective deposition of diamond and diamond patterning while avoiding surface damage associated to diamond-seeding methods.     

Study of the performance of Mo2C for iso-octane steam reforming

In the present work, the performance of commercial molybdenum carbide (Mo₂C) for isooctane steam reforming has been investigated in order to determine the effects of major operating parameters (temperature, space velocity, and steam to carbon ratio) on the catalytic activity. While the results obtained indicate an onset reforming temperature of 850 °C, high concentrations of H₂ in the reforming environment were found to reduce the onset temperature to 750 °C. The catalytic activity at 850 °C was sufficient to produce hydrogen yields greater than 90% and carbon conversions close to 100%, with a low selectivity to CH₄ and CO₂. In addition, and consistent with thermodynamic predictions, a steam to carbon ratio of 1 appeared to optimize the reforming rates. Finally, based on experimental observations, a reaction mechanism was formulated and used to interpret the results obtained during catalytic activity measurements. This mechanism involves continuous oxidation and reduction of Mo metal, which can provide activity and stability to the catalyst when occurring at similar rates.     

Studies on the synthesis of diacetyl over oxidation zeolite catalysts

Diacetyl (2,3-butanedione) synthesis from methyl ethyl ketone over oxidation zeolites using O₂ as oxidant was studied. Various zeolites with Fe, V and Ti as active sites were employed. VS-1, Ti-NCL, Ti-MCM-41 and FeBEA type materials were synthesized and characterized by BET, FTIR, XRD, pyridine adsorption and template desorption. The detailed study of the effect of reaction temperature, the effect of concentration of oxygen and the addition of water was realized. The most active catalyst was zeolites with V as oxidation center.     

A sliding mode control proposal for open-loop unstable processes

This papers presents a sliding mode controller based on a first-order-plus-dead-time model of the process for controlling open-loop unstable systems. The proposed controller has a simple and fixed structure with a set of tuning equations as a function of the desired performance. Both linear and nonlinear models were used to study the controller performance by computer simulations.     

Smith predictor based-sliding mode controller for integrating processes with elevated deadtime

An approach to control integrating processes with elevated deadtime using a Smith predictor sliding mode controller is presented. A PID sliding surface and an integrating first-order plus deadtime model have been used to synthesize the controller. Since the performance of existing controllers with a Smith predictor decrease in the presence of modeling errors, this paper presents a simple approach to combining the Smith predictor with the sliding mode concept, which is a proven, simple, and robust procedure. The proposed scheme has a set of tuning equations as a function of the characteristic parameters of the model. For implementation of our proposed approach, computer based industrial controllers that execute PID algorithms can be used. The performance and robustness of the proposed controller are compared with the Matausek-Mici? scheme for linear systems using simulations.     

Vacuum packed particles as flexible endoscope guides with controllable rigidity

In order to fully benefit from the functionalities of flexible endoscopes in surgery a simple shaft-guide that can be used to support the flexible endoscope shaft is required. Such a shaft-guide must be flexible during insertion into the human body and rigidified when properly positioned to support the flexible endoscope shaft. A shaft-guide called ‘Vacu-SL’ was designed, consisting of a foil tube, filled with particles, that is rigidified by creating a vacuum in its tube. It is expected that the bending stiffness of a loaded, rigidified Vacu-SL shaft-guide is significantly influenced by the shape, hardness and size of the filler particles used. The goal of this study was to find the relations between the filler particles’ size, shape and hardness and a rigidified Vacu-SL shaft-guide’s bending stiffness. Vacu-SL test models were made using polystyrene, acrylic glass, glass, steel, and corundum particles as spheres, pebbles and granulate, with average diameters between 0.16–1.7 mm. These test models were rigidified and then loaded in a tensile tester. The forces needed for 5 and 10 mm deflections of the rigidified test models were measured. The results show that particle size, shape and hardness all influence a rigidified Vacu-SL shaft-guide’s bending stiffness. Size and hardness showed an optimum and granules performed better than spheres. Although the maximally measured bending stiffness might be insufficient to enable proper guidance of flexible endoscope shafts, the results suggest several ways to successfully improve the Vacu-SL shaft-guide.     

Synthesis at several length scales of zeolite A membranes using a continuous flow method

Zeolite A membranes were synthesized in the inner side of porous TiO₂ and α-Al₂O₃ tubular supports by a continuous method. The methodology was then used at several scales for preparing membranes on TiO₂ and α-Al₂O₃ supports with lengths of 6, 12 and 25 cm. Formation of an homogeneous zeolite film was confirmed by XRD and SEM in all supports. Single-gas permeation experiments (He, H₂, N₂ and n-C₃H₈) indicated that Knudsen diffusion was the predominant mechanism in both supports. All the synthesized membranes present high flux and moderate selectivity to water in water–ethanol mixtures.     

The relative positions of alanine residues in the hydrophobic core control the formation of two-stranded or four-stranded {alpha}-helical coiled-coils

The objective of this study was to investigate the positionaleffect of hydrophobic interactions in the -helical interfacein controlling the formation of two-stranded and four-strandedcoiled-coils. Two disulfide-bridged antiparallel coiled-coilswere designed which differ only in the position of a singleAla residue in the middle heptad: in peptide 2H the Ala residuesare in register (in the same rung), while in peptide 4H theyare not. Data from size-exclusion chromatography and sedimentationequilibrium experiments showed that under benign conditionspeptides 2H and 4H were two-stranded and four-stranded coiled-coilsrespectively. These results, in conjunction with molecular modelingstudies, suggest that when four Ala residues are in the sameplane of a potential four-stranded coiled-coil, the small sidechains of Ala would create a large cavity in the hydrophobicinterface of the potential four-stranded structure which isdestabilizing and favors the two-stranded, disulfide-bridgedcoiled-coil. In contrast, an alternating Leu-Ala hydrophobicpacking in the two planes distributes the potential cavity overa larger region, which may be partially filled by minor adjustmentsof the neighboring Leu side chains. As a result, there is stillsufficient hydrophobic contact to maintain the four-strandedstructure.