Hydrogen-transfer catalytic activity of minerals common to coal

The hydrogenation/dehydrogenation catalytic activity of minerals commonly present in coal was investigated. The extent of reaction undergone by the model hydrogen-transfer system tetralin/1,2-dihydronaphthalene/naphthalene at 400 °C in the presence of these minerals was used to measure the catalytic activity. For the four most active minerals, the order of catalytic activity per gram of mineral, for a given range of particle size, is limonites > pyrites > diaspore > magnetites. The pure chemical analog of the limonites, Fe₂O₃, was found to have catalytic activity similar to that of the limonites. Heating the minerals at 400 °C before running the reaction was found to decrease these catalytic activities, despite the surface-area increases resulting from the annealing process. The catalytic activity per unit area of mineral was determined and used as an index of the catalytic activity of the reactive sites for these heterogeneous systems. The order of decreasing site catalytic activity for the more active minerals is pyrites > magnetites > diaspore > limonites. The observed mineral/ chemical compound catalytic activities indicate that the more reactive mineral hydrogenation/ dehydrogenation catalytic sites are composed of iron compounds.     

Molecular Cross-Talk between Gravity- and Light-Sensing Mechanisms in Euglena gracilis

Euglena gracilis is a photosynthetic flagellate. To acquire a suitable position in its surrounding aquatic environment, it exploits light and gravity primarily as environmental cues. Several physiological studies have indicated a fine-tuned relationship between gravity sensing (gravitaxis) and light sensing in E. gracilis. However, the underlying molecular mechanism is largely unknown. The photoreceptor photoactivated adenylyl cyclase (PAC) has been studied for over a decade. Nevertheless, no direct/indirect interaction partner (upstream/downstream) has been reported for PAC. It has been shown that a specific protein, kinase A (PKA), showed to be involved in phototaxis and gravitaxis. The current study reports the localization of the specific PKA and its relationship with PAC.     

Action-research-based optimisation model for health care behaviour change in rural India

In this research, we utilise a multi-method braided approach for a real-world health care intervention in rural India. We first use action research to conceptually underpin the role of self-help groups, disease profiles and appropriate interventions in health care behaviour change and improvement. Action research is then coupled with a non-linear integer-programming-based simulation to determine how health care resources need to be distributed over time, disease type and groups. The action research provides specific research questions and distributional forms needed for the optimisation analysis, while the non-linear integer-programming simulation provides specific recommendations on where and when to distribute resources. External validity of the study is ensured by the adoption of recommendations in the field as part of the action research. Findings from this research have important policy implications. For example, it identifies the value of continuous embedded interventions as opposed to periodic ones and the importance of flexibility in terms of which community groups and disease types to serve over time. This research also provides an important bridge between the operations research, health care in developing nations, organisational theory and humanitarian operations bodies of knowledge.     

Evidence of nano-galvanic couple formation on in-situ formed nano-aluminum amalgam surfaces for passivation-bypassed water splitting

Reaction of Al metal with water is a well-known technique for large scale production of hydrogen. However, this method suffers from kinetic limitations due to formation of a passivation layer on Al, preventing optimal operations. Using high resolution Scanning Kelvin Probe Force Microscopy (SKPFM), we show the origin of formation of 'nano-galvanic couple' on in situ formed nano-aluminum amalgam surfaces in a water splitting system; passivation based limitations are completely bypassed in this approach. Furthermore, they offer an opportunity to beneficiate and recover mercury in contaminated water. The nano-galvanic corrosion due to substantial lateral variation in surface contact potential is responsible for the observed high throughput of hydrogen production (720 mL/min per 0.5 g Al salt). It may be noted that this process fares better than in situ prepared nano-Al based hydrogen production, wherein 600 mL/min of hydrogen is obtained for 0.5 g Al salt. Investigations using Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS) provide evidence for passivation-bypassed hydrolysis and favourable kinetics for in situ derived nano-AlHg hydrolytic agents (when compared to nano-Al). This study, to the best of our knowledge, reports the first direct proof of nano-galvanic couple formation on in-situ prepared nanoaluminum amalgam surface; paving a direct way to overcome the long standing passivation problem in Al hydrolysis. It is found that the hydrogen production rate and standard deviation (SD) of the contact potential of nanoaluminum amalgam are directly related to the rate of addition of the reducing agent, offering an opportunity for kinetic control for the in situ hydrolytic process.     

Comparative studies on the electrochemical and physicochemical behaviour of three different benzimidazole motifs as corrosion inhibitor for mild steel in hydrochloric acid

This paper examines the anticorrosion characteristics of three different benzimidazole derivatives towards mild steel in 0.5?M hydrochloric acid at temperature ranges from 303 to 323?K. The benzimidazole derivatives used for the screening studies are 2-(2-methyl-1H-benzimidazol-1-yl) acethydrazide (EMBAH), 2-(2-ethyl-1H-benzimidazol-1-yl) acethydrazide (EEBAH) and 2-(2-propyl-1H-benzimidazol-1-yl) acethydrazide (EPBAH). The corrosion inhibition was investigated by weight loss, electrochemical impedance spectroscopy and potentiodynamic polarization studies. The adsorption interaction between metal and inhibitor followed Langmuir adsorption isotherm. The Gibb’s free energy values clarify the spontaneous nature of adsorption process. The temperature dependence of inhibition efficiency was explained by considering thermodynamic parameters of adsorption and kinetic parameters of corrosion. These inhibitors showed good efficiency at lower as well as moderately higher temperatures. Quantum chemical calculations were done using DFT at the B3LYP/6-31G¹ level to study the electronic properties of the molecules for correlating the inhibitive effect and molecular structure.     

Fractional Gravitational Grey Wolf Optimization to Multi-Path Data Transmission in IoT

Wireless Personal Communications - The advancements of technology in the field of communication made WSN based IoT attractive and applicable to various areas. It is comprised IoT nodes that work on...     

An ultra-low power high-performance CMOS temperature sensor with an inaccuracy of − 0.3 °C/ + 0.1 °C for aerospace applications

Microsystem Technologies - In the current paper, a new temperature sensor with improved temperature inaccuracy and with very low power consumption has been designed for avionic industry. The...     

Performance and emission characteristics of diesel engine operated on plastic pyrolysis oil with exhaust gas recirculation

The objective of this research was to study the performance and emission characteristics of using waste plastic pyrolysis oil in diesel engine without any engine modification. The engine used in this study is a four-stroke single-cylinder naturally aspirated diesel engine (compression ignition). In the present work, the engine fuelled with blends of diesel fuel (DF) with plastic oil in the ratio of 90:10 (blend10%), 80:20 (blend20%), 70:30 (blend30%), and 50:50 (blend50%) are experimentally measured the efficiencies and emissions, analysed the performance, and compared results with that of DF.     

New pseudo-dynamic analysis of two-layered cohesive-friction soil slope and its numerical validation

Natural slopes consist of non-homogeneous soil profiles with distinct characteristics from slopes made of homogeneous soil. In this study, the limit equilibrium modified pseudo-dynamic method is used to analyze the stability of two-layered c-φ soil slopes in which the failure surface is assumed to be a logarithmic spiral. The zero-stress boundary condition at the ground surface under the seismic loading condition is satisfied. New formulations derived from an analytical method are proposed for the predicting the seismic response in two-layered soil. A detailed parametric study was performed in which various parameters (seismic accelerations, damping, cohesion, and angle of internal friction) were varied. The results of the present method were compared with those in the available literature. The present analytical analysis was also verified against the finite element analysis results.