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In modern society, the multifarious polymeric material polyurethane (PU) is used in household appliances and commercial sectors. Statistics shows the usage of PU as rigid and flexible foams is the highest among different PU-based materials. Industrially viable synthesis, tailor-made porosity and pore morphology, robustness to micro-organisms, weathering, hydrolytic degradation, and resistance to a wide range of chemicals are the excellent attributes of PU foams. Despite achieving significant attention in academia and industries, the prominent tendency to fire-catching or flammability and rapid-fire spread on ignition are the serious concerns of PU foams at their end-use. The figures on home fire accidents and associated fire injuries, loss of civilians, and properties primarily due to fire-catching of furniture are highly devastating. Therefore, a large volume of efforts has been dedicated to decorating flame retardancy in PU foams using a wide range of flame retardants (FRs) (in-situ or post-synthesis). Hence, the focus of this review is to summarize various FRs for rigid and flexible PU foams. The mechanism of flame retardancy, advantages and limitations of various FRs, and the past decade’s advancements achieved concerning the flame retardancy of PU foams have been explored.

The rigid polyurethane foam (PU) is a versatile material, used especially for construction and household applications. The current situation demands a facile, cost-efficient, and greener approach for developing the polyurethanes from bio-derived materials. In this study, we present a novel bio-polyol synthesized using carvone, an extract from caraway, spearmint, or dill seeds via facile thiol-ene reaction. Our one-step reaction uses a UV irradiation to allow the room temperature conversion of the carvone to a high purity bio-polyol, as confirmed from the standard analytical characterizations. The hydroxyl number of 365 mg KOH/g close to its theoretical limit confirms the high conversion yield of the polyol for rigid PU synthesis. To overcome the flammability issues in PU, expandable graphite (EG) powder was used as an additive flame-retardant during the synthesis step. The resulting foams with EG maintained the uniform closed cell structure (>95%) with a high compression strength of 175 kPa. The addition of EG in PU results in the formation of a protective char layer during the flammability test and reduces the weight loss from 40.70% to 3.55% and burning time from 87 to 11 s. Our results confirm that the carvone-based polyol can be a novel alternative to the petroleum polyols for an industrial-scale application.

Energy storage has become increasingly important as a study area in recent decades. A growing number of academics are focusing their attention on developing and researching innovative materials for use in energy storage systems to promote sustainable development goals. This is due to the finite supply of traditional energy sources, such as oil, coal, and natural gas, and escalating regional tensions. Because of these issues, sustainable renewable energy sources have been touted as an alternative to nonrenewable fuels. Deployment of renewable energy sources requires efficient and reliable energy storage devices due to their intermittent nature. High-performance electrochemical energy storage technologies with high power and energy densities are heralded to be the next-generation storage devices. Transition metal chalcogenides (TMCs) have sparked interest among electrode materials because of their intriguing electrochemical properties. Researchers have revealed a variety of modifications to improve their electrochemical performance in energy storage. However, a stronger link between the type of change and the resulting electrochemical performance is still desired. This review examines the synthesis of chalcogenides for electrochemical energy storage devices, their limitations, and the importance of the modification method, followed by a detailed discussion of several modification procedures and how they have helped to improve their electrochemical performance. We also discussed chalcogenides and their composites in batteries and supercapacitors applications. Furthermore, this review discusses the subject’s current challenges as well as potential future opportunities.

Sunflower oil was used for the synthesis of a polyol via an epoxidation reaction followed by a ring-opening reaction. The successful synthesis of the sunflower oil-based polyol (SFO polyol) was demonstrated through structural characterizations and wet-chemistry analysis. Bio-based polyurethane (BPU) films were fabricated using synthesized polyol and diisocyanate. Various amounts of graphene oxide (GO) and reduced graphene oxide (rGO) were added separately to see their effect on the physicomechanical and thermal properties of BPU films. Several tests, such as thermogravimetric analysis, tensile strength, dynamic mechanical analysis, hardness, flexural strength, and the water contact angle, were performed to evaluate the effect of GO and rGO on the properties of the BPU films. Some of the analyses of the BPU films demonstrated an improvement in the mechanical properties, for example, the tensile strength increased from 22.5 to 26 MPa with the addition of only 0.05 wt.% GO. The storage modulus improved from 900 to 1000 and 1700 MPa after the addition of 0.02 and 0.05 wt.% GO, respectively. This study shows that a small amount of GO and rGO could improve the properties of BPU films, making them suitable for use in coating industries.

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