The manufacturing of polystyrene around the globe has escalated in the past years due to its huge applications in various areas. The perpetual market needs of polystyrene led the polystyrene wastes accretion in the landfill causing environmental deterioration. The soaring need for polystyrene also led to the exhaustion of petroleum, a non-renewable energy source, as polystyrene is a petroleum-derived product. Researchers from around the world have discovered a few techniques to take care of the polystyrene scraps, namely recycling and energy recovery techniques. Nevertheless, there are demerits involved with recycling techniques, such as they call for huge labor expenses in the separation process and cause water pollution, thereby decreasing the process sustainability. Owing to these demerits, the researchers have focused their attention on the energy recovery technique. Since petroleum is the main ingredient of polystyrene synthesis, the restoration of liquid oil from polystyrene via the pyrolysis method is a promising technique as the recovered oil has greater calorific value as compared to commercially available fuel. The present paper surveys the pyrolysis technique for polystyrene and the important process parameters that control the end product, like oil, gas, and char. The chief process parameters that are discussed in this review paper include the type of reactors, temperature, residence time, pressure, catalyst types, type of fluidizing gases, and their flow rate. A more recent technique of utilizing a solvent to perform pyrolysis and the effect of various process conditions on the product yield have been discussed. Apart from this, various outlooks to optimize the liquid oil recovery from polystyrene are also reviewed.

The objective of this paper is to present a dynamic Monte Carlo model that is able to simulate the polymerization of styrene with bifunctional free‐radical initiators in a batch reactor. The model can predict the dynamic evolution of the chain length distribution of polystyrene in the reactor. The model includes all relevant polymerization mechanistic steps, including chemical and thermal radical generation, and diffusion‐controlled termination. The model was applied to styrene polymerization and the Monte Carlo estimates for chain length averages were compared to those obtained with the method of moments. Excellent agreement was obtained between the two methods. Although styrene polymerization was used as a case study, the proposed methodology can be easily extended to any other polymer type made by free‐radical polymerization.magnified image

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In this study, we report on the fabrication and utilization of NiCr alloy nanoparticles (NPs)-decorated carbon nanofibers (CNFs) as efficient and competent non-precious catalysts for the hydrolytic dehydrogenation of ammonia borane (AB) at 25 ± 2 °C. The introduced NFs have been fabricated in one step using a high-temperature thermal decomposition of the prepared electrospun nanofiber mats (nickel acetate tetrahydrate, chromium acetate dimer, and polyvinyl alcohol) in an inert atmosphere. The chemical composition of the NFs with different proportions of Ni1−xCrx (x = 0.0, 0.1, 0.15, 0.2, 0.25, 0.3) was established via standard characterization techniques. These techniques proved the formation of disorder Cr2Ni3 alloy and carbon for all the formulations. The as-synthesized composite NFs exhibited a higher catalytic performance for AB dehydrogenation than that of Cr-free Ni–CNFs. Among all the formulations, the sample composed of 15% Cr shows the best catalytic performance, as more H2 was released in less time. Furthermore, it shows good stability, as it is recyclable with little decline in the catalytic activity after six cycles. It also demonstrates the activation energy, entropy (ΔS), and enthalpy (ΔH) with 37.6 kJ/mole, 0.094 kJ/mole, and 35.03 kJ/mole, respectively. Accordingly, the introduced catalyst has a lower price with higher performance encouraging a practical sustainable H2 energy application from the chemical hydrogen storage materials.

At the end of 19th century, the modification of silica has brought revolution in the field of nanocomposites and gained the attention of researchers again by the development of the mesoporous silica class. Silica when used with elastomers provides distinctive characteristics merging the superior properties of inorganic fillers, such as hardness, increased thermal strength, and mechanical stability along with the processability, elasticity, and plasticity of the organic polymers. When carbon black is treated with elastomers instead of silica, it provides greater level of reinforcement because the surface of silica is polar and hydrophilic, but it has greater tendency to adsorb moisture, which affects the ionization of silanol groups. The reason behind switching to silica is adverse effects of carbon black on environment. When silica is added in greater amount, it increases the viscosity of rubbers significantly. The high viscosity causes the processing extra difficult by generating excessive wear and tear over the processing equipment. The increase in viscosity is associated with the strong interaction among the silica particles. It has also been reviewed that the use of silica as filler in elastomers was hindered as far as bifunctional organosilanes were discovered. These are referred to as surface-modifying materials and are initiators for treating silica surfaces to make the filler compatible and friendly to elastomers.

Organic–inorganic metal-halide-based hybrid perovskite solar cells (SCs) have attracted a great deal of attention from researchers around the globe with their certified power conversion efficiencies (PCEs) having now increased to 25.2%. Nevertheless, organic–inorganic hybrid halide perovskite SCs suffer the serious drawback of instability with respect to moisture and heat. However, all-inorganic perovskite SCs have emerged as promising candidates to tackle the thermal instability problem. Since the introduction of all-inorganic perovskite materials to the field of perovskite photovoltaics in 2014, a plethora of research articles has been published focusing on this research topic. The PCE of all-inorganic PSCs has climbed to a record 18.4% and research is underway to enhance this. In this review, I survey the gradual progress of all-inorganic perovskites, their material design, the fabrication of high-quality perovskite films, energetics, major challenges and schemes opening new horizons toward commercialization. Furthermore, techniques to stabilize cubically phased low-bandgap inorganic perovskites are highlighted, as this is an indispensable requirement for stable and highly efficient SCs. In addition, I explain the various energy loss mechanisms at the interface and in the bulk of perovskite and charge-selective layers, and recap previously published reports on the curtailment of charge-carrier recombination losses.

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