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Abstract The evolutionary algorithm of invasive weed optimization algorithm popularly known as the IWO has been used in this paper, to solve the unit commitment (UC) problem. This integer coded algorithm is based on the colonizing behavior of weed plants and has been developed to minimize the total generation cost over a scheduled time period while adhering to several constraints such as generation limits, meeting load demand, spinning reserves and minimum up and down time. The minimum up/down time constraints have been coded in a direct manner without using the penalty function method. The proposed algorithm was tested and validated using 10 units and 24 h system. The most important merit of the proposed methodology is high accuracy and good convergence speed as it is a derivative free algorithm. The simulation results of the proposed algorithm have been compared with the results of other tested algorithms for UC such as shuffled frog leaping, particle swarm optimization, genetic algorithm and Lagrangian relaxation and bacterial foraging algorithm.

The present research was mainly focused on the production of biodiesel from Annona squamosa oil using a synthesized Ni-doped CaO nanocatalyst. The optimization of the transesterification reaction parameters was studied through response surface methodology. The highest biodiesel yield of 99.1% was achieved with the optimized conditions of 7.86% catalyst concentration, 442 RPM, 15.19:1 molar ratio of methanol to oil, reaction temperature of 55.8°C and reaction time of 63.3 min. The results obtained from reaction kinetics study showed a good fit with a first-order kinetic model. The activation energy and R2value were determined to be 53.7 kJ/mol and 0.90, respectively. The synthesized Ni-doped CaO nanocatalyst was characterized using Scanning Electron Microscope with Energy Dispersive X-ray Spectroscopy which confirms the presence of nickel, calcium and oxygen. Also, the average size of the nanocatalyst was found to be 48.79 nm. The Fourier Transform–Infrared Spectroscopy results showed the occurrence of functional groups such as C-H and C = O bonds in the synthesized Ni-doped CaO nanocatalyst. The presence of fatty acid methyl esters in the produced biodiesel was analyzed through Gas Chromatography-Mass Spectrometry analysis. The obtained results from the current study provides the possibility and insights for sustainable biodiesel production and a greener environment.

AbstractNiFe2O4/polythiophene nanocomposite was synthesized by in situ chemical oxidative polymerization of thiophene in NiFe2O4 nanoparticles presence, whereas NiFe2O4 nanoparticles were prepared via coprecipitation method. Fourier transform infrared (FTIR), X‐ray diffraction (XRD), UV–Visible, and SEM, EDX techniques were used for characterization of the nanocomposite. The effect of various parameters such as adsorbent dose, contact time, initial dye concentration, and initial pH of solution on the adsorption of Janus green B (JG) and Fuchsin basic (FB) onto the nanocomposite was optimized by batch studies. The equilibrium uptake data ascribed well to the Langmuir model with maximum adsorption capacity of 143 and 498 mg/g at 303 K for JG and FB, respectively. The exceptional high adsorption capacity of NiFe2O4/polythiophene nanocomposite for JG and FB was ascribed to π‐π and electrostatic interactions. Kinetics studies pointed out that JG and FB removal followed pseudo‐second order model. The negative values of ΔH° (JG: –47.28; FB: −38.00 kJ/mol) and ΔG° (JG: −9.347 to −6.442; FB: −14.16 to – 12.85 kJ/mol) pointed out the feasibility, spontaneity, and exothermic nature of removal process. Negative value of ΔS° (JG: –0.125; FB: –0.078 kJ/mol) suggested decrease in randomness at the solid/liquid interface. The results showed that NiFe2O4/polythiophene is an appealing adsorbent for the uptake of JG and FB dyes from aquatic environment.

Abstract The goal of the safety design for the demonstration fast breeder reactor is to ensure that the safety level is equivalent to or higher than that of the light water reactors of the same period. The design of the safety features such as reactor shutdown, decay heat removal and confinement systems is of importance to reach the goal. The reactor core is equipped with two independent fast shutdown systems, the primary system and the backup system. In addition, it is planned to strengthen the passive shutdown capability by using self- actuated systems such as a Curie point device for the backup system. The decay heat is removed from the core to the atmosphere through the safety lines of the direct reactor auxiliary cooling system which is composed of four independent lines. Furthermore, under the severe conditions that no active function of the decay heat removal system is available, the heat can be removed by natural convection through the safety lines by taking advantage of the high boiling temperature of sodium. For the confinement function, the reactor vessel is surrounded by a containment vessel and a confinement area. The design concept of these safety features is described in this paper.

The development of efficient, low‐cost, non‐noble metal‐oxide‐based nanohybrid materials for overall water splitting is a critical strategy for enhancing clean energy use and addressing environmental issues. In this study, an interfacial engineering strategy for the development of bimetallic Co–Ni nanoparticles on graphitic carbon nitride (g‐C3N4) using ultrasonication followed by coprecipitation is conveyed. These nanoparticles demonstrate high efficacy as bifunctional electrocatalysts for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline conditions. Co–Ni nanoparticles on graphitic carbon nitride demonstrate an increased surface area via ultrasonication and subsequent coprecipitation. The g‐C3N4 combined with Co–Ni nanoparticles leads to the development of bifunctional catalysts that exhibit significant efficiency in both HER and OER, and their interfacial properties are investigated for the first time. The chemical composition and morphology of g‐C3N4 integrated with Co–Ni nanoparticles significantly influence the modulation of redox‐active sites and the facilitation of electron transfer, resulting in improved splitting efficiency. The interactions between the Co–Ni bimetal and g‐C3N4 demonstrate exceptional electrochemical performance for water splitting. Consequently, the 20% 20–Co–Ni–graphitic carbon nitride electrode demonstrated superior HER performance, comparable to the other electrodes. In the results, it is indicated that an increased molar ratio of Co and Ni incorporated in graphitic carbon nitride significantly improves HER performance.

Polymer-based multicolor emissive materials have growing demand due to their potential applications in various fields such as full-color displays, bioimaging, and light sources because of their processability and high stability. Herein, we report dual-color emissive hybrid materials based on biocompatible poly(l-lactide) and polyethylene glycol-modified two-dimensional layered double hydroxide quantum dots (PEG-LDHQDs). The morphology of polymer films tunes the spatial distribution of QDs within the polymer matrix, modulating the energy transfer between the QDs and affording the dual emission behavior in the aggregated states. The amorphous hybrid films show single emission (blue) from the finely dispersed QDs (mostly isolated) within the polymer matrix. In contrast, dual emission (blue and red) was observed when the polymer was crystallized due to the possible accumulation of QDs at the interface of crystalline and amorphous phases in the lamellar structure. Furthermore, the dual emission could be enhanced by the aggregation of QDs on the pores of the breath figure pattern constructed on the surface of the hybrid film.