Effects of MEA fabrication method on durability of polymer electrolyte membrane fuel cells

To study the effects of fabrication methods on the durability of polymer electrolyte membrane fuel cells (PEMFCs), membrane-electrode assemblies (MEAs) were fabricated using a conventional method, a catalyst-coated membrane (CCM) method, and a CCM-hot pressed method. Single cells assembled with the prepared MEAs were operated galvanostatically at 600 mA cm⁻² for 1000 h for the conventional MEA and the CCM MEA and for 500 h for the CCM-hot pressed MEA. During operation, i-V curves, impedance spectra, and cyclic voltammograms were measured roughly every 100 h. Before and after long-term operation, the physical and chemical characteristics of the MEAs were analyzed using mercury porosimetry, X-ray diffraction (XRD), scanning electron microscopy (SEM), electron probe microanalysis (EPMA), and Fourier transformation infrared spectroscopy (FTIR). Under the operating conditions, the CCM MEA exhibited the lowest degradation rate as well as the highest initial performance.     

Effectiveness of parallel joins

The effectiveness of parallel processing of relational join operations is examined. The skew in the distribution of join attribute values and the stochastic nature of the task processing times are identified as the major factors that can affect the effective exploitation of parallelism. Expressions for the execution time of parallel hash join and semijoin are derived and their effectiveness analyzed. When many small processors are used in the parallel architecture, the skew can result in some processors becoming sources of bottleneck while other processors are being underutilized. Even in the absence of skew, the variations in the processing times of the parallel tasks belonging to a query can lead to high task synchronization delay and impact the maximum speedup achievable through parallel execution. For example, when the task processing time on each processor is exponential with the same mean, the speedup is proportional to P/ln(P) where P is the number of processors. Other factors such as memory size, communication bandwidth, etc., can lead to even lower speedup. These are quantified using analytical models     

Research on the engineering geological conditions and stability evaluation of the B2 talus slide at the Jin’an Bridge hydropower station,China

The B2 talus slide at the Jin’an Bridge hydropower station is located on the left bank of the Jinsha River and very close to the left abutment of the dam. The stability of the dam is directly influenced by the engineering geological properties, formation mechanisms, and failure modes of the B2 talus slide. This paper highlights the investigation and analysis of the in situ engineering geological conditions of the slide area. The results indicate that the B2 talus slide is composed of three parts: the talus deposits consisting of a soil-rock mixture (SRM) in the upper part, unloaded and relaxed rock mass in the middle part, and bedrock with several tuff interlayers in the lower part. Based on topographic and geomorphologic analyses, the structure of the rock and soil, distribution characteristics, formation mechanisms, and influencing factors, the strength of the SRM in the upper part and the properties of the tuff interlayer in the lower part are the main factors affecting the stability of the slide. Additionally, the failure modes of the slide are likely to be circular in nature in the talus deposits, broken line sliding along the interface between the unloaded and relaxed rock and the upper boundary of the tuff and broken line sliding along the tuff interlayer. The strength parameters of the SRM and the tuff interlayer were obtained through laboratory experiments and theoretical inverse analyses. Additionally, a three-dimensional geological model of the slide was created using the aforementioned results and the software GoCAD. Limit equilibrium and finite element methods were used to evaluate the stability of the slide using two-dimensional and three-dimensional models. The results indicate that the slope is stable under natural conditions. However, the slope may be unstable, under special conditions, such as artificial excavation, flood discharge atomization, rainstorms, and earthquakes.     

Hydrogen bonding in blends of polyesters with dipeptide‐containing polyphosphazenes

New biomedically erodible polymer composites were investigated. Polyphosphazenes containing the dipeptide side groups alanyl–glycine ethyl ester, valinyl–glycine ethyl ester, and phenylalanyl–glycine ethyl ester were blended with poly(lactide‐co‐glycolide) (PLGA) with lactic to glycolic acid ratios of 50 : 50 [PLGA (50 : 50)] and 85 : 15 [PLGA (85 : 15)] with solution‐phase techniques. Each dipeptide ethyl ester side group contains two N? H protons that are capable of hydrogen bonding with the carbonyl functions of PLGA. Polyphosphazenes that contain only the dipeptide ethyl ester groups are insoluble in organic solvents and are thus unsuitable for solution‐phase composite formation. To ensure solubility during and after synthesis, cosubstituted polymers with both dipeptide ethyl ester and glycine or alanine ethyl ester side groups were used. Solution casting or electrospinning was used to fabricate polymer blend matrices with different ratios of polyphosphazene to polyester, and their miscibilities were estimated with differential scanning calorimetry and scanning electron microscopy techniques. Polyphosphazenes with alanyl–glycine ethyl ester side groups plus the second cosubstituent were completely miscible with PLGA (50 : 50) and PLGA (85 : 15) when processed via solution‐casting techniques. This suggests that the hydrogen‐bonding protons in alanyl–glycine ethyl ester have access to the oxygen atoms of the carbonyl units in PLGA. However, when the same pair of polymers was electrospun from solution, the polymers proved to be immiscible. Solution‐cast miscible polymer blends were obtained from PLGA (50 : 50) plus the polyphosphazene that was cosubstituted with valinyl–glycine ethyl ester and glycine ethyl ester side groups. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Growth of Epitaxial (110) 0.7Pb(Mg<Subscript>1/3</Subscript>Nb<Subscript>2/3</Subscript>)O<Subscript>3</Subscript>-0.3PbTiO<Subscript>3</Subscript> Thin Films on r-Plane Sapphire Substrates by RF Magnetron Sputtering

The role of substrate temperature and substrate surface geometry in determining the crystal structure and crystallinity of 0.7Pb(Mg_1/3Nb_2/3)O₃-0.3PbTiO₃ (PMN-PT) thin films grown on r-plane sapphire substrates is examined. A 30-nm-thick amorphous PMN-PT seed layer deposited at 250°C and subjected to rapid thermal annealing at 850°C results in the formation of an epitaxial (110) perovskite PMN-PT growth template that can be used for subsequent growth of single-crystal (110) perovskite PMN-PT films at elevated temperature. The data show that single-crystal perovskite is promoted when the films nucleate with the \( \langle \overline{1} 11 \rangle \) PMN-PT direction parallel to the \( \langle 0\bar{2}21 \rangle \) Al₂O₃ direction.     

Electromagnetohydrodynamic boundary layer flow in hybrid nanofluid with thermal radiation effect: Numerical simulation

Hybrid nanofluid boundary layer flow past a stretching surface with zero mass flux boundary condition is explored in this article. The main aim of this article is to analyze the electromagnetohydrodynamic role in a hybrid nanofluid containing silver and molybdenum disulfide nanoparticles. The self-similar solution is embedded to reduce the governing partial differential equation into algebraic equations and a shooting algorithm is applied to obtain the solution of the resultant boundary value problem. Variation in momentum, energy, and nanoparticle concentration is explained through graphical profiles. Nusselt number and drag force coefficients are computed for various flow parameters and their impact on the nanofluid and hybrid nanofluid is computed and presented and explained in a comparative fashion. It is observed that the velocity profile shows the opposite nature with respect to the electric field and magnetic field. For electric field parameter velocity accelerates whereas for magnetic parameter velocity diminishes. Nusselt number increases with electric field parameter and nanoparticle volume fraction.     

The pLysRS-Ap4A Pathway in Mast Cells Regulates the Switch from Host Defense to a Pathological State

The innate and adaptive immune systems play an essential role in host defense against pathogens. Various signal transduction pathways monitor and balance the immune system since an imbalance may promote pathological states such as allergy, inflammation, and cancer. Mast cells have a central role in the regulation of the innate/adaptive immune system and are involved in the pathogenesis of many inflammatory and allergic diseases by releasing inflammatory mediators such as histamines, proteases, chemotactic factors, and cytokines. Although various signaling pathways are associated with mast cell activation, our discovery and characterization of the pLysRS-Ap₄A signaling pathway in these cells provided an additional important step towards a full understanding of the intracellular mechanisms involved in mast cell activation. In the present review, we will discuss in depth this signaling pathway’s contribution to host defense and the pathological state.     

REACTIVE EXTRACTION OF LEVULINIC ACID FROM AQUEOUS SOLUTIONS WITH TRI-n-OCTYLAMINE (TOA) IN 1-OCTANOL: EQUILIBRIA,KINETICS, AND MODEL DEVELOPMENT

Levulinic acid, a carboxylic acid containing a ketone structure, can be used as an acidulant in foods and beverages. Reactive extraction is a promising alternative for the recovery of carboxylic acids from aqueous streams. The design of an amine extraction process requires kinetic data for the acid-amine + solvent system used. In this study, equilibrium and kinetic data on the extraction of levulinic acid from aqueous solutions using tri-n-octylamine (TOA) in 1-octanol have been determined. The mass transfer coefficients of levulinic acid, TOA, and 2:1 levulinic acid-amine complex in 1-octanol were calculated from the acetic acid mass transfer coefficient, which was determined by measuring its fluxes of simple diffusion from kerosene to water. Based on the Hatta number and the criterion given by Doraiswamy and Sharma, the reaction regime has been found to be instantaneous reaction regime occurring at the interface on the organic phase side. An extraction model comprising equilibrium complexation constant w.r.t 2:1 levulinic acid-TOA complex formation, K_E2i (14.794 (m³ kmol^?1)²), and complex mass transfer coefficient, k_B2A (2.193 × 10^?6 m s^?1), has been developed.     

Understanding road surface pollutant wash-off and underlying physical processes using simulated rainfall.

Pollutant wash-off is one of the key pollutant processes that detailed knowledge is required in order to develop successful treatment design strategies for urban stormwater. Unfortunately, current knowledge relating to pollutant wash-off is limited. This paper presents the outcomes of a detailed investigation into pollutant wash-off on residential road surfaces. The investigations consisted of research methodologies formulated to overcome the physical constraints due to the heterogeneity of urban paved surfaces and the dependency on naturally occurring rainfall. This entailed the use of small road surface plots and artificially simulated rainfall. Road surfaces were selected due to its critical importance as an urban stormwater pollutant source.The study results showed that the influence of initially available pollutants on the wash-off process was limited. Furthermore, pollutant wash-off from road surfaces can be replicated using an exponential equation. However, the typical version of the exponential wash-off equation needs to be modified by introducing a non dimensional factor referred to as 'capacity factor' CF. Three rainfall intensity ranges were identified where the variation of CF can be defined. Furthermore, it was found that particulate density rather than size is the critical parameter that influences the process of pollutant wash-off.