In this work, the characteristic structure of keratin extracted from two different kinds of industrial waste, namely sheep wool and chicken feathers, using the sulfitolysis method to allow film deposition, has been investigated. The structural and microscopic properties have been studied by means of scanning electron microscopy (SEM), Raman spectroscopy, atomic force microscopy (AFM), and infrared (IR) spectroscopy. Following this, small-angle X-ray scattering (SAXS) analysis for intermediate filaments has been performed. The results indicate that the assembly character of the fiber can be obtained by using the most suitable extraction method, to respond to hydration, thermal, and redox agents. The amorphous part of the fiber and medium range structure is variously affected by the competition between polar bonds (reversible hydrogen bonds) and disulfide bonds (DB), the covalent irreversible ones, and has been investigated by using fine structural methods such as Raman and SAXS, which have depicted in detail the intermediate filaments of keratin from the two different animal origins. The preservation of the secondary structure of the protein obtained does offer a potential for further application of the waste-obtained keratin in polymer films and, possibly, biocomposites.

Introducing lignocellulosic fibers as the matrix reinforcement in composites is an opportunity for weight reduction and also for the use of by-products and biomass waste from other systems, such as agriculture and textiles. In the case of nautical applications, biofouling, meaning damage during service by marine organisms, represents a significant issue. To address this problem, a number of measures can be taken: these include the introduction of various types of fillers, mainly mineral, in composites, tailored treatment of fibers, and hybrid approaches, including a number of different modifications, such as matrix or fiber grafting. This review reports the state of the art in the various studies carried out to elucidate the performance of natural fiber composites and hybrids as regards water absorption and more specifically exposure to seawater for a prolonged time so as to simulate service conditions. The perspectives on the use of natural fiber composites (NFCs) in aquatic environments will be discussed with respect to the possible onset of degradation by biofouling.

The growing demand for sustainable materials has driven the exploration of natural fibers as eco-friendly alternatives to synthetic reinforcements for composites. This study investigates the potential of Posidonia oceanica, an abundant marine biomass, which is often driven to be stacked on the backshore and used so far for energy recovery and low-value applications, as a filler and possible reinforcement in cementitious and polymer composites. Most applications of Posidonia are concentrated in the Mediterranean area and focused on the construction industry. However, its introduction in polymer composites, especially as a source of cellulose or in combination with the use of bio-based matrices, can also be proposed. With this aim, the physical and chemical properties of Posidonia oceanica fibers need to be characterized, and their compatibility with various matrices needs to be evaluated. Experimental results demonstrate that Posidonia oceanica fibers, especially when treated with alkali and silane, or combining both treatments, can exhibit mechanical properties quite comparable to other natural fibers, namely to those obtained from grass species. As with any other type of waste, yet with more interest for its wide accumulation over the coastal line, the use of Posidonia oceanica in composites may contribute to reducing the environmental footprint of these materials, aligning with circular economy principles. This review highlights the dual benefits of utilizing marine biomass by advancing material sustainability while not being detrimental to coastal waste management.

Eumelanin is a black-brown biopigment that provides photoprotection and pigmentation in mammals, insects, and invertebrates. It can be obtained by oxidative polymerisation of 5,6-dihydroxyindole (DHI) and its 2-carboxylic acid (DHICA). Due to its unique physical and chemical properties and its biocompatibility, eumelanin is a promising biomaterial for applications in energy storage, biomedicine, and sensing. However, poor solubility in water and lack of sustainable and low-cost sources of eumelanin have so far limited the full exploitation of this biomaterial. Insect farming is rapidly emerging as an alternative source of eumelanin. Unlike other types of eumelanin, BSF eumelanin, which is extracted from the exoskeleton of the black soldier fly (BSF, Hermetia illucens), is water-dispersible; however, its fundamental chemical properties are not completely understood. Here, we report the characterisation of BSF eumelanin using various spectroscopy techniques. Contrary to what is known about other insect eumelanins, which are believed to contain exclusively DHI, our results indicate that BSF eumelanin may contain both DHI and DHICA moieties. We discuss the potential reasons for this discrepancy.

Black soldier fly (BSF) melanin is a new supply of the brown-black pigment eumelanin. Given that eumelanin is a model bioelectronic material for applications such as medical devices and sensors, understanding BSF melanin’s electrical properties is important to confirm its viability as an advanced material. Presented here is a systematic, hydration dependent alternating current study of BSF melanin utilising both H₂O and D₂O vapours. There is a clear difference between the vapours, enabling a thorough analysis including Nyquist plots with model circuit analysis, broad band dielectric spectroscopic modelling as well as applying the Trukhan model to understand free ion concentration and mobility changes as a function of hydration. We find that BSF melanin behaves similarly to previous reports on synthetic systems, and the analysis here sheds additional light on potential charge transport changes. Significantly, a key finding is that there are two different mobility mechanisms for ion transport depending on hydration.

Field handheld/portable instrumentations, such as in-situ geochemical analyzers, have the potential to assist efficiently targeted geochemical archaeometry campaigns in detecting and quantifying specific elements. Non-destructive portable energy dispersive x-ray fluorescence and micro-destructive handheld laser-induced breakdown spectroscopy (LIBS) instrumentation were utilized to investigate the elemental composition, internal stratigraphy by depth profiling and microscale compositional mapping of five copper and two iron alloy artefacts collected from various ancient graves in the Minervino Murge area, Apulia, Italy. The primary elements identified by both techniques included Cu, Sn and Pb in copper alloys, and Fe with minor amounts of Cu and Pb in iron alloys. Furthermore, the elements Al, Ca, Si, Mg, Na and K, mostly originated from soil contamination, and the trace elements Sb, Ni and Zn were detected. The satisfactory performance of both techniques was assessed by their capacity to provide reproducible elemental composition data. Finally, the depth profile and mapping achieved by LIBS contributed to understanding the metal processing and history of the objects studied, so confirming both techniques to be robust analytical tools in outdoor archaeology and archaeometry campaigns.